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A female, 47-year-old patient underwent treatment for nasolabial folds. Polymethylmethacrylate (PMMA) 10% was injected with a 22 G microcannula. Local anesthesia of lidocaine 2% was administered, then the cannula was introduced through the right oral commissure. At that moment, the patient moved abruptly and reported feeling pain. Although the cannula had already been inserted, the filler had not yet been injected. A retrograde injection of 0.4 mL of PMMA in total was administered. As soon as injected, when removing the cannula, the responsible doctor noticed edema in the region of the nasolabial folds, which spread to the malar region, and the patient reported discomfort at the site. Then, the immediate formation of a small hematoma was observed in the cannula path and, after five minutes, the skin presented a livedoid aspect in the entire cheek region. The protocol for treating occlusion, which consists of severe massage in the region, application of hot compresses, prescription of acetylsalicylic acid (ASA) 300 mg, prednisone 20 mg and prophylactic antibiotic, was started at this moment. The doctor massaged vigorously the region and applied hot compresses. After action was taken, the patient remained in the clinic under observation for approximately one hour. As the patient reported that the pain had ceased, and a relative improvement was observed; she was prescribed antibiotics and sent home.
3.755859
0.984375
sec[1]/sec[0]/p[0]
en
0.999998
34263009
https://doi.org/10.1080/23320885.2021.1933492
[ "region", "cannula", "injected", "nasolabial", "folds", "pmma", "that", "moment", "pain", "doctor" ]
[ { "code": "ND56.0", "title": "Superficial injury of unspecified body region" }, { "code": "ND56.Z", "title": "Unspecified injury to unspecified part of trunk, limb or body region" }, { "code": "CA44", "title": "Pyothorax" }, { "code": "FB3Z", "title": "Disorders of muscles, unspecified" }, { "code": "ND56.8", "title": "Traumatic amputation of unspecified body region" }, { "code": "PL11.2Z", "title": "Embolisation, as mode of injury or harm, unspecified" }, { "code": "QA50", "title": "Embolisation without injury or harm" }, { "code": "EL73.2", "title": "Adverse reaction to injection of neurotoxin" }, { "code": "EL73.0", "title": "Adverse reaction to dermal or deep fillers" }, { "code": "ED6Y", "title": "Other specified disorders of skin pigmentation" } ]
=== ICD-11 CODES FOUND === [ND56.0] Superficial injury of unspecified body region Also known as: Superficial injury of unspecified body region | superficial injury of limb NOS | Superficial injury NOS | scratch NOS | Cutaneous wounds, injuries or scars Excludes: multiple superficial injuries NOS [ND56.Z] Unspecified injury to unspecified part of trunk, limb or body region Also known as: Unspecified injury to unspecified part of trunk, limb or body region | Injury of unspecified body region | injury NOS | trauma NOS | traumatic injury NOS [CA44] Pyothorax Definition: Suppurative inflammation of the pleural space, typically due to acute bacterial infection. It can occur as a complication of pneumonia, thoracotomy, abscesses (lung, hepatic, or subdiaphragmatic), or penetrating trauma with a secondary infection. Also known as: Pyothorax | empyema | pyopneumothorax | Pyothorax with fistula | empyema with fistula Includes: empyema | pyopneumothorax Excludes: due to tuberculosis [FB3Z] Disorders of muscles, unspecified Also known as: Disorders of muscles, unspecified | disorder of muscle, unspecified | muscle disease | muscular disease | muscular disorder [ND56.8] Traumatic amputation of unspecified body region Also known as: Traumatic amputation of unspecified body region | avulsion NOS | Traumatic amputation NOS | traumatic avulsion NOS | traumatic extremity loss Excludes: multiple: crushing injuries NOS | multiple traumatic amputations NOS [PL11.2Z] Embolisation, as mode of injury or harm, unspecified Also known as: Embolisation, as mode of injury or harm, unspecified | Embolisation, as mode of injury or harm | embolic phenomenon as mode of injury | embolism due to intervention | injection of air as mode of injury [QA50] Embolisation without injury or harm Definition: An embolisation without documented injury or harm occurs when a solid object within the venous or arterial circulation propagates to a distal location and becomes lodged there. Also known as: Embolisation without injury or harm | Embolic phenomenon without documented injury or harm | Air embolism without documented injury or harm | Injection of air without injury or harm Excludes: Embolisation, as mode of injury or harm [EL73.2] Adverse reaction to injection of neurotoxin Definition: Adverse event resulting from use of neurotoxins, especially botulinum toxin, into the skin. This is most commonly administered for aesthetic reasons. Recognised problems include ptosis, diplopia and hypersensitivity to the toxin. Details of the reaction should be coded separately. Also known as: Adverse reaction to injection of neurotoxin | Adverse reaction to injection of botulinum toxin [EL73.0] Adverse reaction to dermal or deep fillers Definition: Any adverse event attributable to the use of injected fillers used for soft tissue augmentation. Also known as: Adverse reaction to dermal or deep fillers | Cutaneous necrosis following injection of filler | Foreign body granulomatous reaction to injected filler | Nodule formation attributable to injected filler | Serious adverse reaction to injection of filler Excludes: Pyogenic abscess of the skin [ED6Y] Other specified disorders of skin pigmentation Also known as: Other specified disorders of skin pigmentation | Non-melanin pigmentation due to ingested or injected substance | Carotenoderma | Argyria | Chrysiasis === GRAPH WALKS === --- Walk 1 --- [ND56.0] Superficial injury of unspecified body region --RELATED_TO--> [?] Superficial incisional site infection Def: A surgical site infection involving only skin and subcutaneous tissue of the incision.... --EXCLUDES--> [?] Streptococcal cellulitis of skin --- Walk 2 --- [ND56.0] Superficial injury of unspecified body region --RELATED_TO--> [?] Superficial incisional site infection Def: A surgical site infection involving only skin and subcutaneous tissue of the incision.... --PARENT--> [?] Surgical wound of skin --- Walk 3 --- [ND56.Z] Unspecified injury to unspecified part of trunk, limb or body region --PARENT--> [ND56] Injury of unspecified body region Def: Damage inflicted on the body in an unspecified area as the direct or indirect result of an external force, with or without disruption of structural continuity.... --EXCLUDES--> [?] Injuries involving multiple body regions --- Walk 4 --- [ND56.Z] Unspecified injury to unspecified part of trunk, limb or body region --PARENT--> [ND56] Injury of unspecified body region Def: Damage inflicted on the body in an unspecified area as the direct or indirect result of an external force, with or without disruption of structural continuity.... --CHILD--> [ND56.2] Fracture of unspecified body region --- Walk 5 --- [CA44] Pyothorax Def: Suppurative inflammation of the pleural space, typically due to acute bacterial infection. It can occur as a complication of pneumonia, thoracotomy, abscesses (lung, hepatic, or subdiaphragmatic), or ... --EXCLUDES--> [?] Tuberculous pleurisy, without mention of bacteriological or histological confirmation Def: This is a common, and in many cases lethal, infectious disease caused by various strains of mycobacteria, usually Mycobacterium tuberculosis, with an inflammation of the pleura. This diagnosis is with... --PARENT--> [?] Tuberculosis of the respiratory system Def: This is a progressive or chronic disease resulting from infection with the bacterium Mycobacterium tuberculosis or other bacteria in the M. tuberculosis complex: M. bovis, M. africanum, M. canetti, M.... --- Walk 6 --- [CA44] Pyothorax Def: Suppurative inflammation of the pleural space, typically due to acute bacterial infection. It can occur as a complication of pneumonia, thoracotomy, abscesses (lung, hepatic, or subdiaphragmatic), or ... --EXCLUDES--> [?] Tuberculous pleurisy, without mention of bacteriological or histological confirmation Def: This is a common, and in many cases lethal, infectious disease caused by various strains of mycobacteria, usually Mycobacterium tuberculosis, with an inflammation of the pleura. This diagnosis is with... --CHILD--> [?] Tuberculous empyema, without mention of bacteriological or histological confirmation
[ "[ND56.0] Superficial injury of unspecified body region\n --RELATED_TO--> [?] Superficial incisional site infection\n Def: A surgical site infection involving only skin and subcutaneous tissue of the incision....\n --EXCLUDES--> [?] Streptococcal cellulitis of skin", "[ND56.0] Superficial injury of unspecified body region\n --RELATED_TO--> [?] Superficial incisional site infection\n Def: A surgical site infection involving only skin and subcutaneous tissue of the incision....\n --PARENT--> [?] Surgical wound of skin", "[ND56.Z] Unspecified injury to unspecified part of trunk, limb or body region\n --PARENT--> [ND56] Injury of unspecified body region\n Def: Damage inflicted on the body in an unspecified area as the direct or indirect result of an external force, with or without disruption of structural continuity....\n --EXCLUDES--> [?] Injuries involving multiple body regions", "[ND56.Z] Unspecified injury to unspecified part of trunk, limb or body region\n --PARENT--> [ND56] Injury of unspecified body region\n Def: Damage inflicted on the body in an unspecified area as the direct or indirect result of an external force, with or without disruption of structural continuity....\n --CHILD--> [ND56.2] Fracture of unspecified body region", "[CA44] Pyothorax\n Def: Suppurative inflammation of the pleural space, typically due to acute bacterial infection. It can occur as a complication of pneumonia, thoracotomy, abscesses (lung, hepatic, or subdiaphragmatic), or ...\n --EXCLUDES--> [?] Tuberculous pleurisy, without mention of bacteriological or histological confirmation\n Def: This is a common, and in many cases lethal, infectious disease caused by various strains of mycobacteria, usually Mycobacterium tuberculosis, with an inflammation of the pleura. This diagnosis is with...\n --PARENT--> [?] Tuberculosis of the respiratory system\n Def: This is a progressive or chronic disease resulting from infection with the bacterium Mycobacterium tuberculosis or other bacteria in the M. tuberculosis complex: M. bovis, M. africanum, M. canetti, M....", "[CA44] Pyothorax\n Def: Suppurative inflammation of the pleural space, typically due to acute bacterial infection. It can occur as a complication of pneumonia, thoracotomy, abscesses (lung, hepatic, or subdiaphragmatic), or ...\n --EXCLUDES--> [?] Tuberculous pleurisy, without mention of bacteriological or histological confirmation\n Def: This is a common, and in many cases lethal, infectious disease caused by various strains of mycobacteria, usually Mycobacterium tuberculosis, with an inflammation of the pleura. This diagnosis is with...\n --CHILD--> [?] Tuberculous empyema, without mention of bacteriological or histological confirmation" ]
ND56.0
Superficial injury of unspecified body region
[ { "from_icd11": "ND56.0", "icd10_code": "T009", "icd10_title": "" }, { "from_icd11": "ND56.0", "icd10_code": "T140", "icd10_title": "" }, { "from_icd11": "ND56.Z", "icd10_code": "T1491XA", "icd10_title": "Suicide attempt, initial encounter" }, { "from_icd11": "ND56.Z", "icd10_code": "T1490XS", "icd10_title": "Injury, unspecified, sequela" }, { "from_icd11": "ND56.Z", "icd10_code": "T1490", "icd10_title": "Injury, unspecified" }, { "from_icd11": "ND56.Z", "icd10_code": "T1491", "icd10_title": "Suicide attempt" }, { "from_icd11": "ND56.Z", "icd10_code": "T1490XA", "icd10_title": "Injury, unspecified, initial encounter" }, { "from_icd11": "ND56.Z", "icd10_code": "T148XXS", "icd10_title": "Other injury of unspecified body region, sequela" }, { "from_icd11": "ND56.Z", "icd10_code": "T148XXD", "icd10_title": "Other injury of unspecified body region, subsequent encounter" }, { "from_icd11": "ND56.Z", "icd10_code": "T148", "icd10_title": "Other injury of unspecified body region" }, { "from_icd11": "ND56.Z", "icd10_code": "T14", "icd10_title": "Injury of unspecified body region" }, { "from_icd11": "ND56.Z", "icd10_code": "T149", "icd10_title": "Unspecified injury" }, { "from_icd11": "CA44", "icd10_code": "J869", "icd10_title": "Pyothorax without fistula" }, { "from_icd11": "CA44", "icd10_code": "J860", "icd10_title": "Pyothorax with fistula" }, { "from_icd11": "CA44", "icd10_code": "J85-J86", "icd10_title": "" } ]
T009
Although Patient A experienced mild cough three days before the hospital visit, he did not report this symptom during the entrance screening at the hospital. He had a consultation with a dental surgeon and necessary dental procedures as preparation for orthognathic surgery in the dental clinic from 13:30 to 14:45. He underwent chest X-ray, blood sampling, and facial computed tomography (CT) scanning from 14:45 to 15:20. After that, he returned to the dental department for orthodontic treatment. The first step was pre-consultation examination in the oral and maxillofacial surgery department, which included dental impressions, intraoral photographs, extraoral photographs, dental X-rays, wax bite taking, and face-bow transfer. The second step was face-to-face consultation with a professor and one assistant. The third step was orthodontic treatment in the orthodontic department, including a dental bonding procedure and orthodontic wire change. During these dental procedures, Patient A did not wear a face mask. After all the procedures were over, he was given a verbal summary of future treatment procedures. He left the clinic at 16:40. The next morning, the patient developed dysgeusia and his dry cough worsened. He underwent RT-PCR for SARS-CoV-2. On May 13, 2020, he was confirmed to have SARS-CoV-2 infection. The low Ct value on RT-PCR (22.38 for RdRp and 22.52 for E genes) suggested high viral load.
3.521484
0.983398
sec[2]/sec[0]/p[0]
en
0.999998
34208462
https://doi.org/10.3390/ijerph18126481
[ "dental", "orthodontic", "face", "consultation", "department", "step", "cough", "clinic", "photographs", "sars" ]
[ { "code": "DA07.3", "title": "Disturbances in tooth formation" }, { "code": "DA09.61", "title": "Periapical abscess with sinus" }, { "code": "QA00.8", "title": "Dental examination" }, { "code": "DA08.0", "title": "Dental caries" }, { "code": "DA08.4", "title": "Deposits on teeth" }, { "code": "QB31.2", "title": "Fitting or adjustment of orthodontic device" }, { "code": "QB93", "title": "Contact with health services for orthodontic care" }, { "code": "ED90.1", "title": "Periorificial dermatitis" }, { "code": "8B88.0", "title": "Bell palsy" }, { "code": "LA51", "title": "Facial clefts" } ]
=== ICD-11 CODES FOUND === [DA07.3] Disturbances in tooth formation Definition: A group of conditions characterised by disturbances in tooth formation. Also known as: Disturbances in tooth formation | disturbance of tooth formation | Dental dysplasia | disorder of tooth formation | Florid cemento-osseous dysplasia Includes: Dental dysplasia | Florid cemento-osseous dysplasia | Regional odontodysplasia Excludes: Hutchinson teeth and mulberry molars in congenital syphilis | mottled teeth [DA09.61] Periapical abscess with sinus Also known as: Periapical abscess with sinus | Dental abscess with sinus | Dentoalveolar abscess with sinus | Dental sinus | periapical abscess fistula Includes: Dental abscess with sinus | Dentoalveolar abscess with sinus | Dental sinus [QA00.8] Dental examination Also known as: Dental examination | examination of teeth [DA08.0] Dental caries Definition: A condition characterised by localised destruction of calcified tissue, initiated on the tooth surface by decalcification of the enamel, followed by the enzymatic lysis of organic structures, resulting in cavity formation. Also known as: Dental caries | Dental decay | carious teeth | dental cavity | saprodontia Includes: Dental decay [DA08.4] Deposits on teeth Definition: In dentistry, calculus or tartar is a form of hardened dental plaque. Also known as: Deposits on teeth | Accretions on teeth | Extrinsic staining of teeth NOS | staining of teeth NOS | Betel deposits on teeth [QB31.2] Fitting or adjustment of orthodontic device Also known as: Fitting or adjustment of orthodontic device | fitting of orthodontics | orthodontics adjustment [QB93] Contact with health services for orthodontic care Also known as: Contact with health services for orthodontic care | orthodontic aftercare [ED90.1] Periorificial dermatitis Definition: Periorificial dermatitis is a term which links two erythematous and papulopustular facial dermatoses that are strongly linked to prolonged potent topical corticosteroid use, namely perioral dermatitis and periocular dermatitis. It is characterised by the development of erythema, papules and pustules in perioral and periocular skin. Also known as: Periorificial dermatitis | Perioral dermatitis | Corticosteroid-induced perioral dermatitis | Periocular dermatitis | Periorificial dermatitis of eyelids [8B88.0] Bell palsy Also known as: Bell palsy | Facial nerve paralysis | Facial nerve palsy | Seventh cranial nerve paralysis | facial palsy [LA51] Facial clefts Definition: Any condition caused by failure of the structures of the face to correctly develop during the antenatal period. These conditions are characterised by a partition in bone, soft tissue, or skin of the face. Also known as: Facial clefts | Craniofacial clefts | Median facial cleft | Tessier number 0-14 and 30 facial cleft | Midline facial cleft Excludes: Frontofacionasal dysostosis | Frontonasal dysplasia === GRAPH WALKS === --- Walk 1 --- [DA07.3] Disturbances in tooth formation Def: A group of conditions characterised by disturbances in tooth formation.... --EXCLUDES--> [?] Mottling of enamel Def: Mottling occurs only when the dentition is permanently exposed to excessive fluoride during the development calcification of teeth.... --PARENT--> [?] Fluoride related opacities or lesions Def: This is a fluoride related abnormality in the tissue of an organism (in layman's terms, "damage"), usually caused by disease or trauma.... --- Walk 2 --- [DA07.3] Disturbances in tooth formation Def: A group of conditions characterised by disturbances in tooth formation.... --EXCLUDES--> [?] Mottling of enamel Def: Mottling occurs only when the dentition is permanently exposed to excessive fluoride during the development calcification of teeth.... --PARENT--> [?] Fluoride related opacities or lesions Def: This is a fluoride related abnormality in the tissue of an organism (in layman's terms, "damage"), usually caused by disease or trauma.... --- Walk 3 --- [DA09.61] Periapical abscess with sinus --PARENT--> [DA09.6] Periapical abscess --CHILD--> [DA09.61] Periapical abscess with sinus --- Walk 4 --- [DA09.61] Periapical abscess with sinus --PARENT--> [DA09.6] Periapical abscess --CHILD--> [DA09.61] Periapical abscess with sinus --- Walk 5 --- [QA00.8] Dental examination --PARENT--> [QA00] General examination or investigation of persons without complaint or reported diagnosis --EXCLUDES--> [?] Special screening examination for neoplasms --- Walk 6 --- [QA00.8] Dental examination --PARENT--> [QA00] General examination or investigation of persons without complaint or reported diagnosis --EXCLUDES--> [?] Special screening examination for neoplasms
[ "[DA07.3] Disturbances in tooth formation\n Def: A group of conditions characterised by disturbances in tooth formation....\n --EXCLUDES--> [?] Mottling of enamel\n Def: Mottling occurs only when the dentition is permanently exposed to excessive fluoride during the development calcification of teeth....\n --PARENT--> [?] Fluoride related opacities or lesions\n Def: This is a fluoride related abnormality in the tissue of an organism (in layman's terms, \"damage\"), usually caused by disease or trauma....", "[DA07.3] Disturbances in tooth formation\n Def: A group of conditions characterised by disturbances in tooth formation....\n --EXCLUDES--> [?] Mottling of enamel\n Def: Mottling occurs only when the dentition is permanently exposed to excessive fluoride during the development calcification of teeth....\n --PARENT--> [?] Fluoride related opacities or lesions\n Def: This is a fluoride related abnormality in the tissue of an organism (in layman's terms, \"damage\"), usually caused by disease or trauma....", "[DA09.61] Periapical abscess with sinus\n --PARENT--> [DA09.6] Periapical abscess\n --CHILD--> [DA09.61] Periapical abscess with sinus", "[DA09.61] Periapical abscess with sinus\n --PARENT--> [DA09.6] Periapical abscess\n --CHILD--> [DA09.61] Periapical abscess with sinus", "[QA00.8] Dental examination\n --PARENT--> [QA00] General examination or investigation of persons without complaint or reported diagnosis\n --EXCLUDES--> [?] Special screening examination for neoplasms", "[QA00.8] Dental examination\n --PARENT--> [QA00] General examination or investigation of persons without complaint or reported diagnosis\n --EXCLUDES--> [?] Special screening examination for neoplasms" ]
DA07.3
Disturbances in tooth formation
[ { "from_icd11": "DA07.3", "icd10_code": "K004", "icd10_title": "Disturbances in tooth formation" }, { "from_icd11": "DA09.61", "icd10_code": "K046", "icd10_title": "Periapical abscess with sinus" }, { "from_icd11": "QA00.8", "icd10_code": "Z012", "icd10_title": "Encounter for dental examination and cleaning" }, { "from_icd11": "DA08.0", "icd10_code": "K027", "icd10_title": "Dental root caries" }, { "from_icd11": "DA08.0", "icd10_code": "K0263", "icd10_title": "Dental caries on smooth surface penetrating into pulp" }, { "from_icd11": "DA08.0", "icd10_code": "K0253", "icd10_title": "Dental caries on pit and fissure surface penetrating into pulp" }, { "from_icd11": "DA08.0", "icd10_code": "K029", "icd10_title": "Dental caries, unspecified" }, { "from_icd11": "DA08.0", "icd10_code": "K02", "icd10_title": "Dental caries" }, { "from_icd11": "DA08.0", "icd10_code": "K020", "icd10_title": "" }, { "from_icd11": "DA08.0", "icd10_code": "K021", "icd10_title": "" }, { "from_icd11": "DA08.0", "icd10_code": "K022", "icd10_title": "" }, { "from_icd11": "DA08.0", "icd10_code": "K023", "icd10_title": "Arrested dental caries" }, { "from_icd11": "DA08.0", "icd10_code": "K024", "icd10_title": "" }, { "from_icd11": "DA08.0", "icd10_code": "K025", "icd10_title": "Dental caries on pit and fissure surface" }, { "from_icd11": "DA08.0", "icd10_code": "K028", "icd10_title": "" } ]
K004
Disturbances in tooth formation
Th1 helper cell secretion of interferon gamma (IFNγ) is of pivotal significance for the activation of monocytes to establish an effective host defense against intracellular pathogens . Genetic defects of IFNγ signaling (e.g. affecting the IFNγ receptor or the transcription factor STAT1 [ 3 – 7 ]) thus lead to congenital immunodeficiency syndromes with susceptibility to infections with intracellular pathogens, particularly mycobacteria . In human immunodeficiency virus (HIV)-uninfected adults however, an acquired susceptibility to intracellular pathogens is rare. In 2004, high-titer neutralizing autoantibodies against IFNγ were first identified as the cause of an acquired immunodeficiency syndrome subsequently termed adult-onset immunodeficiency with anti-interferon-gamma autoantibodies (AIIA) [ 8 , 10 – 12 ]. This syndrome is characterized by a disturbed IFNγ signalling pathway leading to recurrent and disseminated infections with non-tuberculous mycobacteria (NTM), non-typhoidal salmonella , cytomegalovirus (CMV), varicella zoster virus (VZV) and other pathogens. Diagnosis of AIIA can be challenging as it involves specific testing not routinely available and clinical presentations can be unusual. We here report a rare case of a patient presenting with the nearly complete spectrum of simultaneous infections typical for this condition, where diagnosis was delayed by a misguiding secondary finding.
4.355469
0.878418
sec[0]/p[0]
en
0.999998
33176707
https://doi.org/10.1186/s12879-020-05553-y
[ "pathogens", "immunodeficiency", "intracellular", "infections", "interferon", "gamma", "against", "susceptibility", "mycobacteria", "virus" ]
[ { "code": "4A00.2", "title": "Genetic susceptibility to particular pathogens" }, { "code": "1A03.0", "title": "Enteropathogenic Escherichia coli infection" }, { "code": "4B4Z", "title": "Diseases of the immune system, unspecified" }, { "code": "4A0Z", "title": "Primary immunodeficiencies, unspecified" }, { "code": "4A20.Z", "title": "Acquired immunodeficiencies, unspecified" }, { "code": "4A01.1Z", "title": "Combined immunodeficiencies, unspecified" }, { "code": "4A0Y", "title": "Other specified primary immunodeficiencies" }, { "code": "1B21.0", "title": "Pulmonary infection due to non-tuberculous mycobacterium" }, { "code": "1B21.2Y&XN5LZ", "title": "Cutaneous Mycobacterium avium-intracellulare infection" }, { "code": "1B21.3", "title": "Disseminated non-tuberculous mycobacterial infection" } ]
=== ICD-11 CODES FOUND === [4A00.2] Genetic susceptibility to particular pathogens Also known as: Genetic susceptibility to particular pathogens | Idiopathic CD4 lymphocytopenia | Immunodeficiency due to interleukin-1 receptor-associated kinase-4 deficiency | IRAK4 - [interleukin-1 receptor-associated kinase-4 deficiency] | Lung fibrosis - immunodeficiency - gonadal dysgenesis [1A03.0] Enteropathogenic Escherichia coli infection Definition: An infection of the gastrointestinal system, caused by the gram-negative bacteria Escherichia coli. It is characterised by acute, profuse, watery diarrhoea. Transmission is by the faecal-oral route from contaminated food, water, or fomites. Confirmation is by identification of enteropathogenic Escherichia coli (EPEC) in a faecal sample. Also known as: Enteropathogenic Escherichia coli infection | EPEC - [Enteropathogenic Escherichia coli] infection | Enteritis in enteropathogenic Escherichia coli infection | Colitis in enteropathogenic Escherichia coli infection [4B4Z] Diseases of the immune system, unspecified Also known as: Diseases of the immune system, unspecified | immunological defect NOS | immunity disorder NOS | immune mechanism disorder NOS | immune compromised NOS [4A0Z] Primary immunodeficiencies, unspecified Also known as: Primary immunodeficiencies, unspecified [4A20.Z] Acquired immunodeficiencies, unspecified Also known as: Acquired immunodeficiencies, unspecified | Acquired immunodeficiencies [4A01.1Z] Combined immunodeficiencies, unspecified Also known as: Combined immunodeficiencies, unspecified | Combined immunodeficiencies | Combined T and B cell immunodeficiency | combined immunity deficiency | combined immunodeficiency syndrome [4A0Y] Other specified primary immunodeficiencies Also known as: Other specified primary immunodeficiencies | Lymphocyte function antigen-1 [LFA-1] defect [1B21.0] Pulmonary infection due to non-tuberculous mycobacterium Definition: A condition of the pulmonary system, caused by an infection with the bacteria Mycobacterium (excluding infections due to Mycobacterium tuberculosis and Mycobacterium leprae). This disease is characterised by cough, fever, weight loss, and fatigue. Transmission is by direct contact with Mycobacterium in the environment. Also known as: Pulmonary infection due to non-tuberculous mycobacterium | pulmonary mycobacterium infection | pulmonary diseases due to other mycobacteria | pulmonary nontuberculous mycobacteriosis | atypical mycobacterium pulmonary infection Includes: Pulmonary infection due to Mycobacterium avium-intracellulare complex | Pulmonary infection due to Mycobacterium kansasii | Pulmonary infection due to Mycobacterium xenopi [1B21.3] Disseminated non-tuberculous mycobacterial infection Also known as: Disseminated non-tuberculous mycobacterial infection | Disseminated Mycobacterium avium-intracellulare infection | DMAC - [disseminated mycobacterium avium-intracellulare complex infection] === GRAPH WALKS === --- Walk 1 --- [4A00.2] Genetic susceptibility to particular pathogens --RELATED_TO--> [?] Encephalitis due to herpes simplex virus Def: Herpetic encephalitis is a cerebral infection caused by herpes simplex virus type 1 (HSV1). It presents as acute necrosing temporal encephalitis. Onset is rapid (less than 48 hours) with a fever of 40... --CHILD--> [?] Herpesviral meningoencephalitis --- Walk 2 --- [4A00.2] Genetic susceptibility to particular pathogens --RELATED_TO--> [?] Chronic mucocutaneous candidosis Def: Chronic Mucocutaneous Candidiasis is a primary immune deficiency characterised by persistent and/or recurrent infections of skin, nails and mucous membranes, caused by organisms of the genus Candida, ... --PARENT--> [?] Candidosis of skin or mucous membranes --- Walk 3 --- [1A03.0] Enteropathogenic Escherichia coli infection Def: An infection of the gastrointestinal system, caused by the gram-negative bacteria Escherichia coli. It is characterised by acute, profuse, watery diarrhoea. Transmission is by the faecal-oral route fr... --PARENT--> [1A03] Intestinal infections due to Escherichia coli Def: Any condition of the gastrointestinal system, caused by an infection with the gram-negative bacteria Escherichia coli.... --CHILD--> [1A03.0] Enteropathogenic Escherichia coli infection Def: An infection of the gastrointestinal system, caused by the gram-negative bacteria Escherichia coli. It is characterised by acute, profuse, watery diarrhoea. Transmission is by the faecal-oral route fr... --- Walk 4 --- [1A03.0] Enteropathogenic Escherichia coli infection Def: An infection of the gastrointestinal system, caused by the gram-negative bacteria Escherichia coli. It is characterised by acute, profuse, watery diarrhoea. Transmission is by the faecal-oral route fr... --PARENT--> [1A03] Intestinal infections due to Escherichia coli Def: Any condition of the gastrointestinal system, caused by an infection with the gram-negative bacteria Escherichia coli.... --PARENT--> [?] Bacterial intestinal infections Def: Any condition of the intestines, caused by an infection with a bacterial source.... --- Walk 5 --- [4B4Z] Diseases of the immune system, unspecified --PARENT--> [04] Diseases of the immune system --RELATED_TO--> [?] Symptoms, signs or clinical findings of blood, blood-forming organs, or the immune system --- Walk 6 --- [4B4Z] Diseases of the immune system, unspecified --PARENT--> [04] Diseases of the immune system --PARENT--> [?] ICD-11 for Mortality and Morbidity Statistics
[ "[4A00.2] Genetic susceptibility to particular pathogens\n --RELATED_TO--> [?] Encephalitis due to herpes simplex virus\n Def: Herpetic encephalitis is a cerebral infection caused by herpes simplex virus type 1 (HSV1). It presents as acute necrosing temporal encephalitis. Onset is rapid (less than 48 hours) with a fever of 40...\n --CHILD--> [?] Herpesviral meningoencephalitis", "[4A00.2] Genetic susceptibility to particular pathogens\n --RELATED_TO--> [?] Chronic mucocutaneous candidosis\n Def: Chronic Mucocutaneous Candidiasis is a primary immune deficiency characterised by persistent and/or recurrent infections of skin, nails and mucous membranes, caused by organisms of the genus Candida, ...\n --PARENT--> [?] Candidosis of skin or mucous membranes", "[1A03.0] Enteropathogenic Escherichia coli infection\n Def: An infection of the gastrointestinal system, caused by the gram-negative bacteria Escherichia coli. It is characterised by acute, profuse, watery diarrhoea. Transmission is by the faecal-oral route fr...\n --PARENT--> [1A03] Intestinal infections due to Escherichia coli\n Def: Any condition of the gastrointestinal system, caused by an infection with the gram-negative bacteria Escherichia coli....\n --CHILD--> [1A03.0] Enteropathogenic Escherichia coli infection\n Def: An infection of the gastrointestinal system, caused by the gram-negative bacteria Escherichia coli. It is characterised by acute, profuse, watery diarrhoea. Transmission is by the faecal-oral route fr...", "[1A03.0] Enteropathogenic Escherichia coli infection\n Def: An infection of the gastrointestinal system, caused by the gram-negative bacteria Escherichia coli. It is characterised by acute, profuse, watery diarrhoea. Transmission is by the faecal-oral route fr...\n --PARENT--> [1A03] Intestinal infections due to Escherichia coli\n Def: Any condition of the gastrointestinal system, caused by an infection with the gram-negative bacteria Escherichia coli....\n --PARENT--> [?] Bacterial intestinal infections\n Def: Any condition of the intestines, caused by an infection with a bacterial source....", "[4B4Z] Diseases of the immune system, unspecified\n --PARENT--> [04] Diseases of the immune system\n --RELATED_TO--> [?] Symptoms, signs or clinical findings of blood, blood-forming organs, or the immune system", "[4B4Z] Diseases of the immune system, unspecified\n --PARENT--> [04] Diseases of the immune system\n --PARENT--> [?] ICD-11 for Mortality and Morbidity Statistics" ]
4A00.2
Genetic susceptibility to particular pathogens
[ { "from_icd11": "4A00.2", "icd10_code": "D848", "icd10_title": "Other specified immunodeficiencies" }, { "from_icd11": "1A03.0", "icd10_code": "A040", "icd10_title": "Enteropathogenic Escherichia coli infection" }, { "from_icd11": "4B4Z", "icd10_code": "D8940", "icd10_title": "Mast cell activation, unspecified" }, { "from_icd11": "4B4Z", "icd10_code": "D8949", "icd10_title": "Other mast cell activation disorder" }, { "from_icd11": "4B4Z", "icd10_code": "D892", "icd10_title": "Hypergammaglobulinemia, unspecified" }, { "from_icd11": "4B4Z", "icd10_code": "D8942", "icd10_title": "Idiopathic mast cell activation syndrome" }, { "from_icd11": "4B4Z", "icd10_code": "D8982", "icd10_title": "Autoimmune lymphoproliferative syndrome [ALPS]" }, { "from_icd11": "4B4Z", "icd10_code": "D89813", "icd10_title": "Graft-versus-host disease, unspecified" }, { "from_icd11": "4B4Z", "icd10_code": "D89810", "icd10_title": "Acute graft-versus-host disease" }, { "from_icd11": "4B4Z", "icd10_code": "D89811", "icd10_title": "Chronic graft-versus-host disease" }, { "from_icd11": "4B4Z", "icd10_code": "D8989", "icd10_title": "Other specified disorders involving the immune mechanism, not elsewhere classified" }, { "from_icd11": "4B4Z", "icd10_code": "D89812", "icd10_title": "Acute on chronic graft-versus-host disease" }, { "from_icd11": "4B4Z", "icd10_code": "D891", "icd10_title": "Cryoglobulinemia" }, { "from_icd11": "4B4Z", "icd10_code": "D899", "icd10_title": "Disorder involving the immune mechanism, unspecified" }, { "from_icd11": "4B4Z", "icd10_code": "D80-D89", "icd10_title": "" } ]
D848
Other specified immunodeficiencies
We discussed this clinical case during one active learning session (student’s case conference, MD academic year 3, Nazarbayev University School of Medicine) during the pediatric clerkship, and some important aspects were highlighted. The main point was that, in front of the confirmed radiological picture of bronchiectasis and the important personal history of recurrent respiratory infections, the patient never received an immunological work-up. Therefore, the simple measurement of serum immunoglobulins (IgA, IgG, IgM and IgE) was recommended, in addition to the sweat test for cystic fibrosis: as reported in Table 2 , hypogammaglobulinemia with severe reduction of IgG and total IgA deficiency (without hyper-IgM and hyper-IgE findings) was evidenced, which was consistent with a diagnosis of CVID. Indeed, no absolute cellular deficiency was detected by the following cytofluorimetry analysis of the main lymphocyte subpopulations (CD3+CD8+, CD3+CD4+, CD19+, CD16+CD56+). Accordingly, the patient started the replacement therapy with intra-venous immunoglobulin (IVIG, 0.4 g/kg, every 28 days). After one year since this treatment, this patient showed a significant reduction of the infectious episodes; unfortunately, no precise and confirmed information about the respiratory function and lung radiological picture are available at the moment, since the patient is currently followed at the regional hospital.
3.992188
0.969238
sec[1]/p[5]
en
0.999998
34449684
https://doi.org/10.3390/pediatric13030055
[ "this", "important", "main", "radiological", "picture", "respiratory", "reduction", "deficiency", "hyper", "since" ]
[ { "code": "4A01.03", "title": "Transient hypogammaglobulinaemia of infancy" }, { "code": "5C53.31", "title": "Mitochondrial protein import disorders" }, { "code": "1C81", "title": "Acute poliomyelitis" }, { "code": "LA8B.1", "title": "Congenital anomaly of pulmonary arterial tree" }, { "code": "FA31.6", "title": "Acquired clawhand or clubhand" }, { "code": "2D70", "title": "Malignant neoplasm metastasis in lung" }, { "code": "2C25.Z", "title": "Malignant neoplasms of bronchus or lung, unspecified" }, { "code": "2E62.2", "title": "Carcinoma in situ of bronchus or lung" }, { "code": "QA00.B", "title": "Radiological examination" }, { "code": "PK8Y", "title": "Other specified surgical or other medical procedures associated with injury or harm in diagnostic or therapeutic use" } ]
=== ICD-11 CODES FOUND === [4A01.03] Transient hypogammaglobulinaemia of infancy Also known as: Transient hypogammaglobulinaemia of infancy | immunoglobulin maturational delay | THI - [transient hypogammaglobulinaemia of infancy] [5C53.31] Mitochondrial protein import disorders Definition: This refers to disorders in the enzyme that belongs to the family of hydrolases, specifically those acting on acid anhydrides to catalyse transmembrane movement of substances. Also known as: Mitochondrial protein import disorders [1C81] Acute poliomyelitis Definition: A disease of the nervous system, caused by human poliovirus. This disease commonly presents with a fever, sore throat, headache, vomiting, or stiffness of the neck and back. This disease may present with an acute onset of flaccid paralysis. Transmission is commonly by the faecal-oral route or direct contact. Confirmation is by identification of poliovirus in a faecal sample or by a lumbar puncture. Also known as: Acute poliomyelitis | acute spinal poliomyelitis | polio NOS | PM - [poliomyelitis] | Heine-Medin disease [LA8B.1] Congenital anomaly of pulmonary arterial tree Definition: A congenital cardiovascular malformation of the pulmonary trunk (main pulmonary artery) and/or branch pulmonary arteries (right, left, and ramifications). Also known as: Congenital anomaly of pulmonary arterial tree | Aberrant pulmonary artery | abnormal origin of pulmonary artery | Anomaly of pulmonary artery | congenital malposition of pulmonary artery Includes: Aberrant pulmonary artery | Anomaly of pulmonary artery [FA31.6] Acquired clawhand or clubhand Also known as: Acquired clawhand or clubhand | Acquired clawhand | main en griffe | Acquired clubhand [2D70] Malignant neoplasm metastasis in lung Also known as: Malignant neoplasm metastasis in lung | metastasis in lung | pulmonary metastasis | secondary cancer in lung | secondary malignant tumour in lung Excludes: Malignant neoplasms of bronchus or lung [2C25.Z] Malignant neoplasms of bronchus or lung, unspecified Also known as: Malignant neoplasms of bronchus or lung, unspecified | Malignant neoplasms of bronchus or lung | malignant pulmonary adenomatosis of unspecified site | superior sulcus malignant tumour | bronchiole cancer [2E62.2] Carcinoma in situ of bronchus or lung Also known as: Carcinoma in situ of bronchus or lung | Intraepithelial neoplasia (dysplasia) of bronchus and lung, high grade | Carcinoma in situ of bronchus | bronchial in situ carcinoma | carcinoma in situ of carina [QA00.B] Radiological examination Also known as: Radiological examination | Routine chest X-ray Excludes: Special screening examination for neoplasm of breast [PK8Y] Other specified surgical or other medical procedures associated with injury or harm in diagnostic or therapeutic use Also known as: Other specified surgical or other medical procedures associated with injury or harm in diagnostic or therapeutic use | Diagnostic imaging procedures associated with injury or harm | complication of radiological procedure | radiological procedure associated with abnormal reaction of the patient, or of later complication, without mention of misadventure at the time of the procedure === GRAPH WALKS === --- Walk 1 --- [4A01.03] Transient hypogammaglobulinaemia of infancy --PARENT--> [4A01.0] Immunodeficiencies with predominantly antibody defects Def: A disorder characterised by an inability to mount a normal immune response due to antibody (i.e. immunoglobulin) defects... --PARENT--> [4A01] Primary immunodeficiencies due to disorders of adaptive immunity --- Walk 2 --- [4A01.03] Transient hypogammaglobulinaemia of infancy --PARENT--> [4A01.0] Immunodeficiencies with predominantly antibody defects Def: A disorder characterised by an inability to mount a normal immune response due to antibody (i.e. immunoglobulin) defects... --CHILD--> [4A01.02] Specific antibody deficiency with normal immunoglobulin concentrations or normal number of B cells --- Walk 3 --- [5C53.31] Mitochondrial protein import disorders Def: This refers to disorders in the enzyme that belongs to the family of hydrolases, specifically those acting on acid anhydrides to catalyse transmembrane movement of substances.... --RELATED_TO--> [?] Deafness-dystonia optic atrophy syndrome Def: An X-linked neurodegenerative syndrome characterized by prelingual or postlingual sensorineural hearing loss, progressive dystonia and visual impairment. In addition, psychiatric symptoms, cognitive i... --PARENT--> [?] Mitochondrial protein import disorders Def: This refers to disorders in the enzyme that belongs to the family of hydrolases, specifically those acting on acid anhydrides to catalyse transmembrane movement of substances.... --- Walk 4 --- [5C53.31] Mitochondrial protein import disorders Def: This refers to disorders in the enzyme that belongs to the family of hydrolases, specifically those acting on acid anhydrides to catalyse transmembrane movement of substances.... --PARENT--> [5C53.3] Disorders of mitochondrial membrane transport Def: An inborn error of metabolism in proteins in the membranes of mitochondria, which serve to transport molecules and other factors such as ions into or out of the organelles... --CHILD--> [5C53.3Y] Other specified disorders of mitochondrial membrane transport --- Walk 5 --- [1C81] Acute poliomyelitis Def: A disease of the nervous system, caused by human poliovirus. This disease commonly presents with a fever, sore throat, headache, vomiting, or stiffness of the neck and back. This disease may present w... --PARENT--> [?] Viral infections of the central nervous system Def: Any disease of the central nervous system, caused by an infection with a viral source.... --RELATED_TO--> [?] Enteroviral exanthematous fever Def: An acute febrile, characteristically morbilliform exanthem due to infection by one of many different enteroviruses, especially Coxsackievirus and Echovirus.... --- Walk 6 --- [1C81] Acute poliomyelitis Def: A disease of the nervous system, caused by human poliovirus. This disease commonly presents with a fever, sore throat, headache, vomiting, or stiffness of the neck and back. This disease may present w... --PARENT--> [?] Viral infections of the central nervous system Def: Any disease of the central nervous system, caused by an infection with a viral source.... --RELATED_TO--> [?] Progressive multifocal leukoencephalopathy
[ "[4A01.03] Transient hypogammaglobulinaemia of infancy\n --PARENT--> [4A01.0] Immunodeficiencies with predominantly antibody defects\n Def: A disorder characterised by an inability to mount a normal immune response due to antibody (i.e. immunoglobulin) defects...\n --PARENT--> [4A01] Primary immunodeficiencies due to disorders of adaptive immunity", "[4A01.03] Transient hypogammaglobulinaemia of infancy\n --PARENT--> [4A01.0] Immunodeficiencies with predominantly antibody defects\n Def: A disorder characterised by an inability to mount a normal immune response due to antibody (i.e. immunoglobulin) defects...\n --CHILD--> [4A01.02] Specific antibody deficiency with normal immunoglobulin concentrations or normal number of B cells", "[5C53.31] Mitochondrial protein import disorders\n Def: This refers to disorders in the enzyme that belongs to the family of hydrolases, specifically those acting on acid anhydrides to catalyse transmembrane movement of substances....\n --RELATED_TO--> [?] Deafness-dystonia optic atrophy syndrome\n Def: An X-linked neurodegenerative syndrome characterized by prelingual or postlingual sensorineural hearing loss, progressive dystonia and visual impairment. In addition, psychiatric symptoms, cognitive i...\n --PARENT--> [?] Mitochondrial protein import disorders\n Def: This refers to disorders in the enzyme that belongs to the family of hydrolases, specifically those acting on acid anhydrides to catalyse transmembrane movement of substances....", "[5C53.31] Mitochondrial protein import disorders\n Def: This refers to disorders in the enzyme that belongs to the family of hydrolases, specifically those acting on acid anhydrides to catalyse transmembrane movement of substances....\n --PARENT--> [5C53.3] Disorders of mitochondrial membrane transport\n Def: An inborn error of metabolism in proteins in the membranes of mitochondria, which serve to transport molecules and other factors such as ions into or out of the organelles...\n --CHILD--> [5C53.3Y] Other specified disorders of mitochondrial membrane transport", "[1C81] Acute poliomyelitis\n Def: A disease of the nervous system, caused by human poliovirus. This disease commonly presents with a fever, sore throat, headache, vomiting, or stiffness of the neck and back. This disease may present w...\n --PARENT--> [?] Viral infections of the central nervous system\n Def: Any disease of the central nervous system, caused by an infection with a viral source....\n --RELATED_TO--> [?] Enteroviral exanthematous fever\n Def: An acute febrile, characteristically morbilliform exanthem due to infection by one of many different enteroviruses, especially Coxsackievirus and Echovirus....", "[1C81] Acute poliomyelitis\n Def: A disease of the nervous system, caused by human poliovirus. This disease commonly presents with a fever, sore throat, headache, vomiting, or stiffness of the neck and back. This disease may present w...\n --PARENT--> [?] Viral infections of the central nervous system\n Def: Any disease of the central nervous system, caused by an infection with a viral source....\n --RELATED_TO--> [?] Progressive multifocal leukoencephalopathy" ]
4A01.03
Transient hypogammaglobulinaemia of infancy
[ { "from_icd11": "4A01.03", "icd10_code": "D807", "icd10_title": "Transient hypogammaglobulinemia of infancy" }, { "from_icd11": "1C81", "icd10_code": "A809", "icd10_title": "Acute poliomyelitis, unspecified" }, { "from_icd11": "1C81", "icd10_code": "A80", "icd10_title": "Acute poliomyelitis" }, { "from_icd11": "1C81", "icd10_code": "A800", "icd10_title": "Acute paralytic poliomyelitis, vaccine-associated" }, { "from_icd11": "1C81", "icd10_code": "A801", "icd10_title": "Acute paralytic poliomyelitis, wild virus, imported" }, { "from_icd11": "1C81", "icd10_code": "A802", "icd10_title": "Acute paralytic poliomyelitis, wild virus, indigenous" }, { "from_icd11": "1C81", "icd10_code": "A803", "icd10_title": "Acute paralytic poliomyelitis, other and unspecified" }, { "from_icd11": "1C81", "icd10_code": "A804", "icd10_title": "Acute nonparalytic poliomyelitis" }, { "from_icd11": "LA8B.1", "icd10_code": "Q2572", "icd10_title": "Congenital pulmonary arteriovenous malformation" }, { "from_icd11": "LA8B.1", "icd10_code": "Q2579", "icd10_title": "Other congenital malformations of pulmonary artery" }, { "from_icd11": "LA8B.1", "icd10_code": "Q2571", "icd10_title": "Coarctation of pulmonary artery" }, { "from_icd11": "LA8B.1", "icd10_code": "Q256", "icd10_title": "Stenosis of pulmonary artery" }, { "from_icd11": "LA8B.1", "icd10_code": "Q257", "icd10_title": "Other congenital malformations of pulmonary artery" }, { "from_icd11": "2D70", "icd10_code": "C7800", "icd10_title": "Secondary malignant neoplasm of unspecified lung" }, { "from_icd11": "2D70", "icd10_code": "C780", "icd10_title": "Secondary malignant neoplasm of lung" } ]
D807
Transient hypogammaglobulinemia of infancy
The second case is a 53-year-old female patient, without relevant pathological history, diagnosed with primary ocular diffuse large B cell lymphoma, stage IE (right eye), at the Jules Bordet Institute in Brussels, Belgium. The clinical presentation showed weight loss and granulomatous bilateral anterior uveitis, manifested with altered visual acuity. At diagnosis, the MYD88 L265P mutation was detected, which is associated with non-Hodgkin’s lymphomas with poor overall survival (OS). The patient was treated with intraocular administration of methotrexate (MTX) and rituximab, associated with MATRIX regimen (without thiotepa), administered for 6 cycles. Unfortunately, after 2 month of finishing chemotherapy, the lymphoma affected the patient’s left eye. The patient presented with severe and fast cognitive degradation and after a second biopsy, diagnosis of PCNSL was confirmed, it having infiltrated both frontal lobes. The second-line therapy was ibrutinib (560 mg/day), a treatment which continued for 4 months. The control MRI performed in July and September of the same year depicted demyelination of the white substance in frontal left lobe, but with remission of the CNS tumoral masses. The patient still presents headache, but PET scan made in September reveals complete metabolic remission and she is currently eligible for autologous stem cell transplantation (ASCT) in a secondary transplant center .
3.970703
0.981934
sec[1]/p[3]
en
0.999997
34640501
https://doi.org/10.3390/jcm10194483
[ "without", "cell", "lymphoma", "which", "associated", "frontal", "september", "remission", "relevant", "pathological" ]
[ { "code": "MH12.1", "title": "Death occurring less than 24 hours from onset of symptoms, not otherwise explained" }, { "code": "FA36.Y", "title": "Other specified effusion of joint" }, { "code": "3A51.1", "title": "Sickle cell disease without crisis" }, { "code": "QA50", "title": "Embolisation without injury or harm" }, { "code": "LB12.1Z", "title": "Atresia of oesophagus, unspecified" }, { "code": "MF9Y", "title": "Other specified clinical findings on examination of urine, without diagnosis" }, { "code": "5C56.20", "title": "Mucolipidosis" }, { "code": "9A96.3", "title": "Primary anterior uveitis" }, { "code": "3A61.Z", "title": "Acquired pure red cell aplasia, unspecified" }, { "code": "2B33.5", "title": "Malignant lymphoma, not elsewhere classified" } ]
=== ICD-11 CODES FOUND === [MH12.1] Death occurring less than 24 hours from onset of symptoms, not otherwise explained Also known as: Death occurring less than 24 hours from onset of symptoms, not otherwise explained | died without sign of disease | Death known not to be violent or instantaneous for which no cause can be discovered | death known not to be violent or instantaneous, cause unknown | Death without sign of disease Includes: Death known not to be violent or instantaneous for which no cause can be discovered | Death without sign of disease [FA36.Y] Other specified effusion of joint Also known as: Other specified effusion of joint | Non aspirated effusion of joint | Effusion of joint without blood | Effusion of joint, multiple sites | Effusion of joint, shoulder region [3A51.1] Sickle cell disease without crisis Definition: A disorder caused by a HbS mutation in the haemoglobin gene. This disorder is characterised by abnormal rigid sickle-shaped red blood cells decreasing its ability to carry oxygen. This disorder may present with fatigue, shortness of breath, dizziness, headaches, pallor of skin or mucous membranes, and jaundice. This disorder is confirmed by identification of HbS mutation by genetic testing. Also known as: Sickle cell disease without crisis | Hb-SS disease without crisis | HbSS without crisis | Sickle-cell anaemia without crisis | SCD - [sickle cell disease] [QA50] Embolisation without injury or harm Definition: An embolisation without documented injury or harm occurs when a solid object within the venous or arterial circulation propagates to a distal location and becomes lodged there. Also known as: Embolisation without injury or harm | Embolic phenomenon without documented injury or harm | Air embolism without documented injury or harm | Injection of air without injury or harm Excludes: Embolisation, as mode of injury or harm [LB12.1Z] Atresia of oesophagus, unspecified Also known as: Atresia of oesophagus, unspecified | Atresia of oesophagus | atresia of esophagus | Atresia of oesophagus without fistula | congenital atresia of oesophagus [MF9Y] Other specified clinical findings on examination of urine, without diagnosis Also known as: Other specified clinical findings on examination of urine, without diagnosis | Methaemoglobinuria | Other and unspecified abnormal findings in urine | Calciuria | Cells and casts in urine [5C56.20] Mucolipidosis Also known as: Mucolipidosis | Mucolipidosis type 3 | Pseudo-Hurler polydystrophy | Pseudo-Hurler disease | Mucolipidosis type 2 Excludes: Sialidosis (mucolipidosis type 1) [9A96.3] Primary anterior uveitis Definition: This refers to primary inflammation of the uvea. The uvea consists of the middle, pigmented, vascular structures of the eye and includes the iris, ciliary body, and choroid. Also known as: Primary anterior uveitis | anterior chamber cell [3A61.Z] Acquired pure red cell aplasia, unspecified Also known as: Acquired pure red cell aplasia, unspecified | Acquired pure red cell aplasia | acquired red cell aplasia | red cell aplasia NOS | pure red cell aplastic anaemia [2B33.5] Malignant lymphoma, not elsewhere classified Also known as: Malignant lymphoma, not elsewhere classified | Lymphoma NOS | NHL - [non-Hodgkin lymphoma] | non-Hodgkin lymphoma | Non-Hodgkin lymphoma, NOS === GRAPH WALKS === --- Walk 1 --- [MH12.1] Death occurring less than 24 hours from onset of symptoms, not otherwise explained --PARENT--> [MH12] Other sudden death, cause unknown --CHILD--> [MH12.0] Instantaneous death --- Walk 2 --- [MH12.1] Death occurring less than 24 hours from onset of symptoms, not otherwise explained --PARENT--> [MH12] Other sudden death, cause unknown --CHILD--> [MH12.Y] Other specified sudden death, cause unknown --- Walk 3 --- [FA36.Y] Other specified effusion of joint --PARENT--> [FA36] Effusion of joint Def: Increased intra-articular fluid secondary to trauma and/or other acquired conditions not detailed in other codes.... --CHILD--> [FA36.0] Effusion of joint containing blood --- Walk 4 --- [FA36.Y] Other specified effusion of joint --PARENT--> [FA36] Effusion of joint Def: Increased intra-articular fluid secondary to trauma and/or other acquired conditions not detailed in other codes.... --CHILD--> [FA36.0] Effusion of joint containing blood --- Walk 5 --- [3A51.1] Sickle cell disease without crisis Def: A disorder caused by a HbS mutation in the haemoglobin gene. This disorder is characterised by abnormal rigid sickle-shaped red blood cells decreasing its ability to carry oxygen. This disorder may pr... --PARENT--> [3A51] Sickle cell disorders or other haemoglobinopathies Def: Any disorder caused by a HbS mutation in the haemoglobin gene. This disorder is characterised by abnormal rigid sickle-shaped red blood cells decreasing its ability to carry oxygen. This disorder may ... --RELATED_TO--> [?] Other sickle-cell disorders with retinopathy Def: This is an autosomal recessive genetic blood disorder with overdominance, characterised by red blood cells that assume an abnormal, rigid, sickle shape. This diagnosis is due to persistent or acute da... --- Walk 6 --- [3A51.1] Sickle cell disease without crisis Def: A disorder caused by a HbS mutation in the haemoglobin gene. This disorder is characterised by abnormal rigid sickle-shaped red blood cells decreasing its ability to carry oxygen. This disorder may pr... --PARENT--> [3A51] Sickle cell disorders or other haemoglobinopathies Def: Any disorder caused by a HbS mutation in the haemoglobin gene. This disorder is characterised by abnormal rigid sickle-shaped red blood cells decreasing its ability to carry oxygen. This disorder may ... --CHILD--> [3A51.1] Sickle cell disease without crisis Def: A disorder caused by a HbS mutation in the haemoglobin gene. This disorder is characterised by abnormal rigid sickle-shaped red blood cells decreasing its ability to carry oxygen. This disorder may pr...
[ "[MH12.1] Death occurring less than 24 hours from onset of symptoms, not otherwise explained\n --PARENT--> [MH12] Other sudden death, cause unknown\n --CHILD--> [MH12.0] Instantaneous death", "[MH12.1] Death occurring less than 24 hours from onset of symptoms, not otherwise explained\n --PARENT--> [MH12] Other sudden death, cause unknown\n --CHILD--> [MH12.Y] Other specified sudden death, cause unknown", "[FA36.Y] Other specified effusion of joint\n --PARENT--> [FA36] Effusion of joint\n Def: Increased intra-articular fluid secondary to trauma and/or other acquired conditions not detailed in other codes....\n --CHILD--> [FA36.0] Effusion of joint containing blood", "[FA36.Y] Other specified effusion of joint\n --PARENT--> [FA36] Effusion of joint\n Def: Increased intra-articular fluid secondary to trauma and/or other acquired conditions not detailed in other codes....\n --CHILD--> [FA36.0] Effusion of joint containing blood", "[3A51.1] Sickle cell disease without crisis\n Def: A disorder caused by a HbS mutation in the haemoglobin gene. This disorder is characterised by abnormal rigid sickle-shaped red blood cells decreasing its ability to carry oxygen. This disorder may pr...\n --PARENT--> [3A51] Sickle cell disorders or other haemoglobinopathies\n Def: Any disorder caused by a HbS mutation in the haemoglobin gene. This disorder is characterised by abnormal rigid sickle-shaped red blood cells decreasing its ability to carry oxygen. This disorder may ...\n --RELATED_TO--> [?] Other sickle-cell disorders with retinopathy\n Def: This is an autosomal recessive genetic blood disorder with overdominance, characterised by red blood cells that assume an abnormal, rigid, sickle shape. This diagnosis is due to persistent or acute da...", "[3A51.1] Sickle cell disease without crisis\n Def: A disorder caused by a HbS mutation in the haemoglobin gene. This disorder is characterised by abnormal rigid sickle-shaped red blood cells decreasing its ability to carry oxygen. This disorder may pr...\n --PARENT--> [3A51] Sickle cell disorders or other haemoglobinopathies\n Def: Any disorder caused by a HbS mutation in the haemoglobin gene. This disorder is characterised by abnormal rigid sickle-shaped red blood cells decreasing its ability to carry oxygen. This disorder may ...\n --CHILD--> [3A51.1] Sickle cell disease without crisis\n Def: A disorder caused by a HbS mutation in the haemoglobin gene. This disorder is characterised by abnormal rigid sickle-shaped red blood cells decreasing its ability to carry oxygen. This disorder may pr..." ]
MH12.1
Death occurring less than 24 hours from onset of symptoms, not otherwise explained
[ { "from_icd11": "MH12.1", "icd10_code": "R961", "icd10_title": "" }, { "from_icd11": "3A51.1", "icd10_code": "D571", "icd10_title": "Sickle-cell disease without crisis" }, { "from_icd11": "QA50", "icd10_code": "XXI", "icd10_title": "" }, { "from_icd11": "3A61.Z", "icd10_code": "D609", "icd10_title": "Acquired pure red cell aplasia, unspecified" }, { "from_icd11": "3A61.Z", "icd10_code": "D608", "icd10_title": "Other acquired pure red cell aplasias" }, { "from_icd11": "3A61.Z", "icd10_code": "D60", "icd10_title": "Acquired pure red cell aplasia [erythroblastopenia]" }, { "from_icd11": "2B33.5", "icd10_code": "C8593", "icd10_title": "Non-Hodgkin lymphoma, unspecified, intra-abdominal lymph nodes" }, { "from_icd11": "2B33.5", "icd10_code": "C8592", "icd10_title": "Non-Hodgkin lymphoma, unspecified, intrathoracic lymph nodes" }, { "from_icd11": "2B33.5", "icd10_code": "C8591", "icd10_title": "Non-Hodgkin lymphoma, unspecified, lymph nodes of head, face, and neck" }, { "from_icd11": "2B33.5", "icd10_code": "C8599", "icd10_title": "Non-Hodgkin lymphoma, unspecified, extranodal and solid organ sites" }, { "from_icd11": "2B33.5", "icd10_code": "C8598", "icd10_title": "Non-Hodgkin lymphoma, unspecified, lymph nodes of multiple sites" }, { "from_icd11": "2B33.5", "icd10_code": "C8594", "icd10_title": "Non-Hodgkin lymphoma, unspecified, lymph nodes of axilla and upper limb" }, { "from_icd11": "2B33.5", "icd10_code": "C8597", "icd10_title": "Non-Hodgkin lymphoma, unspecified, spleen" }, { "from_icd11": "2B33.5", "icd10_code": "C8590", "icd10_title": "Non-Hodgkin lymphoma, unspecified, unspecified site" }, { "from_icd11": "2B33.5", "icd10_code": "C857", "icd10_title": "" } ]
R961
Our patient’s presentation was caused by severe constipation. Our literature review identified one case of ACS in an adult caused by constipation likely secondary to neurogenic bowel 8 and two cases thought to be due to clozapine use. 9 Her longstanding constipation was likely due to her medication regimen of clozapine, risperidone, and the anticholinergic medications glycopyrrolate and benztropine. Clozapine is effective for treatment-resistant schizophrenia but is prescribed uncommonly . 10 In a meta-analysis from 2016, constipation was reported in 31% of patients taking clozapine, nearly three times more than patients taking other antipsychotics. 11 A recent study of reports concerning clozapine to the Australian Therapeutic Goods Administration and New Zealand Pharmacovigilance Center found an 18% mortality rate over 22 years in patients with gastrointestinal adverse reactions serious enough to require hospitalization or surgical intervention. The same study reported data from a World Health Organization registry with a case fatality rate of 13% for the complaint of constipation. Case fatality rates were higher when sequela of constipation such as intestinal obstruction (25%) and intestinal ischemia (68%) were reported. 12 It is unknown whether ACS was diagnosed in any of those patients. Risperidone, glycopyrrolate, and benztropine have also been implicated as causes for constipation. 13 – 15
4.148438
0.675781
sec[2]/p[2]
en
0.999996
35226838
https://doi.org/10.5811/cpcem.2021.7.53295
[ "constipation", "clozapine", "patients", "caused", "likely", "risperidone", "glycopyrrolate", "benztropine", "taking", "fatality" ]
[ { "code": "ME05.0", "title": "Constipation" }, { "code": "DD91.1", "title": "Functional constipation" }, { "code": "DB32.1", "title": "Slow transit constipation" }, { "code": "DD93.Y", "title": "Other functional digestive disorders of infants, neonates or toddlers" }, { "code": "DD91.00", "title": "Irritable bowel syndrome, constipation predominant" }, { "code": "NE60", "title": "Harmful effects of drugs, medicaments or biological substances, not elsewhere classified" }, { "code": "PL14.C", "title": "Patient received diagnostic test or treatment intended for another patient" }, { "code": "QB14", "title": "Unavailability or inaccessibility of health care facilities" }, { "code": "PL14.2", "title": "Problem associated with physical transfer of patient" }, { "code": "QB12.0", "title": "Organ transplant candidate" } ]
=== ICD-11 CODES FOUND === [ME05.0] Constipation Definition: Constipation is an acute or chronic condition in which bowel movements occur less often than usual or consist of hard, dry stools that are often painful or difficult to pass. Here constipation other than specifically described elsewhere, such as in motility disorders of intestine or in functional bowel diseases, is described. Also known as: Constipation | faecal impaction | constipated | chronic constipation with overflow | difficult passing motion Includes: faecal impaction Excludes: Functional constipation | Functional constipation of infants, toddlers or children | Atonic constipation [DD91.1] Functional constipation Definition: Functional constipation is a functional bowel disorder that presents as persistently difficult, infrequent, or seemingly incomplete defecation, which do not meet IBS criteria. Also known as: Functional constipation | neurogenic constipation | spastic constipation | functional constipation with slow transit | Atonic constipation Excludes: Constipation NOS [DB32.1] Slow transit constipation Definition: Slow transit constipation (STC) typically involves the unusually slow passage of luminal contents through the large intestine. This can lead to chronic problems, such as constipation and uncontrollable soiling and could require colectomy. Also known as: Slow transit constipation | STC - [slow-transit constipation] | Colonic inertia [DD93.Y] Other functional digestive disorders of infants, neonates or toddlers Also known as: Other functional digestive disorders of infants, neonates or toddlers | Functional vomiting or aerophagia in childhood | Adolescent rumination syndrome | rumination syndrome in children | Cyclic vomiting syndrome in children [DD91.00] Irritable bowel syndrome, constipation predominant Definition: This is a bowel pattern subtype of irritable bowel syndrome, characterised by alteration of bowel habits with constipation predominant. Also known as: Irritable bowel syndrome, constipation predominant | IBS-C - [Irritable bowel syndrome, constipation predominant] [NE60] Harmful effects of drugs, medicaments or biological substances, not elsewhere classified Also known as: Harmful effects of drugs, medicaments or biological substances, not elsewhere classified | drugs, medicaments or biological substances, toxicity not elsewhere classified | adverse drug effects | drug reaction NOS | drug allergy NOS Excludes: Alcohol intoxication | pathological drug intoxication | hypersensitivity reaction to correctly administered drug [PL14.C] Patient received diagnostic test or treatment intended for another patient Also known as: Patient received diagnostic test or treatment intended for another patient | wrong patient | incorrect patient Excludes: Procedure undertaken at wrong site or wrong side, as mode of injury or harm [QB14] Unavailability or inaccessibility of health care facilities Also known as: Unavailability or inaccessibility of health care facilities | unavailability of medical facilities | Unavailability of outpatient clinic | Unavailability or inaccessibility of residential aged care service Excludes: bed unavailable [PL14.2] Problem associated with physical transfer of patient Also known as: Problem associated with physical transfer of patient [QB12.0] Organ transplant candidate Also known as: Organ transplant candidate | patient waiting for organ availability | health services provided because of need for organ transplant | organ transplant candidate awaiting organ availability | person on organ transplant waiting list === GRAPH WALKS === --- Walk 1 --- [ME05.0] Constipation Def: Constipation is an acute or chronic condition in which bowel movements occur less often than usual or consist of hard, dry stools that are often painful or difficult to pass. Here constipation other t... --EXCLUDES--> [?] Atonic constipation --PARENT--> [?] Functional constipation Def: Functional constipation is a functional bowel disorder that presents as persistently difficult, infrequent, or seemingly incomplete defecation, which do not meet IBS criteria.... --- Walk 2 --- [ME05.0] Constipation Def: Constipation is an acute or chronic condition in which bowel movements occur less often than usual or consist of hard, dry stools that are often painful or difficult to pass. Here constipation other t... --EXCLUDES--> [?] Functional constipation of infants, toddlers or children Def: This is a functional bowel disorder of infants, toddlers and children that presents as persistently difficult, infrequent, or seemingly incomplete defecation, which do not meet IBS criteria.... --PARENT--> [?] Functional digestive disorders of infants, toddlers or children Def: This group incorporates functional gastrointestinal disorders in infants and toddlers and disorders diagnosed more often in school-aged children and adolescents. These disorders include a variable com... --- Walk 3 --- [DD91.1] Functional constipation Def: Functional constipation is a functional bowel disorder that presents as persistently difficult, infrequent, or seemingly incomplete defecation, which do not meet IBS criteria.... --RELATED_TO--> [?] Slow transit constipation Def: Slow transit constipation (STC) typically involves the unusually slow passage of luminal contents through the large intestine. This can lead to chronic problems, such as constipation and uncontrollabl... --PARENT--> [?] Motility disorders of large intestine Def: Disorders of colonic motility due to abnormal contractions, such as spasms and colonic paralysis. The loss of ability to coordinate motor activity may cause a variety of disorders including colonic di... --- Walk 4 --- [DD91.1] Functional constipation Def: Functional constipation is a functional bowel disorder that presents as persistently difficult, infrequent, or seemingly incomplete defecation, which do not meet IBS criteria.... --EXCLUDES--> [?] Constipation Def: Constipation is an acute or chronic condition in which bowel movements occur less often than usual or consist of hard, dry stools that are often painful or difficult to pass. Here constipation other t... --EXCLUDES--> [?] Atonic constipation --- Walk 5 --- [DB32.1] Slow transit constipation Def: Slow transit constipation (STC) typically involves the unusually slow passage of luminal contents through the large intestine. This can lead to chronic problems, such as constipation and uncontrollabl... --PARENT--> [DB32] Motility disorders of large intestine Def: Disorders of colonic motility due to abnormal contractions, such as spasms and colonic paralysis. The loss of ability to coordinate motor activity may cause a variety of disorders including colonic di... --RELATED_TO--> [?] Paralytic ileus of large intestine Def: Paralytic ileus of large intestine is a decreased motor activity of colon due to non-mechanical causes. The intestinal paralysis need not be complete, but it must be sufficient to prohibit the passage... --- Walk 6 --- [DB32.1] Slow transit constipation Def: Slow transit constipation (STC) typically involves the unusually slow passage of luminal contents through the large intestine. This can lead to chronic problems, such as constipation and uncontrollabl... --PARENT--> [DB32] Motility disorders of large intestine Def: Disorders of colonic motility due to abnormal contractions, such as spasms and colonic paralysis. The loss of ability to coordinate motor activity may cause a variety of disorders including colonic di... --CHILD--> [DB32.2] Megacolon Def: Megacolon is a descriptive term indicating an abnormal dilation of large intestine. The dilatation is often accompanied by a paralysis of the peristaltic movements of the bowel....
[ "[ME05.0] Constipation\n Def: Constipation is an acute or chronic condition in which bowel movements occur less often than usual or consist of hard, dry stools that are often painful or difficult to pass. Here constipation other t...\n --EXCLUDES--> [?] Atonic constipation\n --PARENT--> [?] Functional constipation\n Def: Functional constipation is a functional bowel disorder that presents as persistently difficult, infrequent, or seemingly incomplete defecation, which do not meet IBS criteria....", "[ME05.0] Constipation\n Def: Constipation is an acute or chronic condition in which bowel movements occur less often than usual or consist of hard, dry stools that are often painful or difficult to pass. Here constipation other t...\n --EXCLUDES--> [?] Functional constipation of infants, toddlers or children\n Def: This is a functional bowel disorder of infants, toddlers and children that presents as persistently difficult, infrequent, or seemingly incomplete defecation, which do not meet IBS criteria....\n --PARENT--> [?] Functional digestive disorders of infants, toddlers or children\n Def: This group incorporates functional gastrointestinal disorders in infants and toddlers and disorders diagnosed more often in school-aged children and adolescents. These disorders include a variable com...", "[DD91.1] Functional constipation\n Def: Functional constipation is a functional bowel disorder that presents as persistently difficult, infrequent, or seemingly incomplete defecation, which do not meet IBS criteria....\n --RELATED_TO--> [?] Slow transit constipation\n Def: Slow transit constipation (STC) typically involves the unusually slow passage of luminal contents through the large intestine. This can lead to chronic problems, such as constipation and uncontrollabl...\n --PARENT--> [?] Motility disorders of large intestine\n Def: Disorders of colonic motility due to abnormal contractions, such as spasms and colonic paralysis. The loss of ability to coordinate motor activity may cause a variety of disorders including colonic di...", "[DD91.1] Functional constipation\n Def: Functional constipation is a functional bowel disorder that presents as persistently difficult, infrequent, or seemingly incomplete defecation, which do not meet IBS criteria....\n --EXCLUDES--> [?] Constipation\n Def: Constipation is an acute or chronic condition in which bowel movements occur less often than usual or consist of hard, dry stools that are often painful or difficult to pass. Here constipation other t...\n --EXCLUDES--> [?] Atonic constipation", "[DB32.1] Slow transit constipation\n Def: Slow transit constipation (STC) typically involves the unusually slow passage of luminal contents through the large intestine. This can lead to chronic problems, such as constipation and uncontrollabl...\n --PARENT--> [DB32] Motility disorders of large intestine\n Def: Disorders of colonic motility due to abnormal contractions, such as spasms and colonic paralysis. The loss of ability to coordinate motor activity may cause a variety of disorders including colonic di...\n --RELATED_TO--> [?] Paralytic ileus of large intestine\n Def: Paralytic ileus of large intestine is a decreased motor activity of colon due to non-mechanical causes. The intestinal paralysis need not be complete, but it must be sufficient to prohibit the passage...", "[DB32.1] Slow transit constipation\n Def: Slow transit constipation (STC) typically involves the unusually slow passage of luminal contents through the large intestine. This can lead to chronic problems, such as constipation and uncontrollabl...\n --PARENT--> [DB32] Motility disorders of large intestine\n Def: Disorders of colonic motility due to abnormal contractions, such as spasms and colonic paralysis. The loss of ability to coordinate motor activity may cause a variety of disorders including colonic di...\n --CHILD--> [DB32.2] Megacolon\n Def: Megacolon is a descriptive term indicating an abnormal dilation of large intestine. The dilatation is often accompanied by a paralysis of the peristaltic movements of the bowel...." ]
ME05.0
Constipation
[ { "from_icd11": "ME05.0", "icd10_code": "K5900", "icd10_title": "Constipation, unspecified" }, { "from_icd11": "ME05.0", "icd10_code": "K5909", "icd10_title": "Other constipation" }, { "from_icd11": "DD91.1", "icd10_code": "K5903", "icd10_title": "Drug induced constipation" }, { "from_icd11": "DD91.1", "icd10_code": "K5901", "icd10_title": "Slow transit constipation" }, { "from_icd11": "DD91.1", "icd10_code": "K5904", "icd10_title": "Chronic idiopathic constipation" }, { "from_icd11": "DD91.1", "icd10_code": "K5902", "icd10_title": "Outlet dysfunction constipation" }, { "from_icd11": "DD91.1", "icd10_code": "K590", "icd10_title": "Constipation" }, { "from_icd11": "DD91.00", "icd10_code": "K582", "icd10_title": "Mixed irritable bowel syndrome" }, { "from_icd11": "NE60", "icd10_code": "T50A95A", "icd10_title": "Adverse effect of other bacterial vaccines, initial encounter" }, { "from_icd11": "NE60", "icd10_code": "T50Z15A", "icd10_title": "Adverse effect of immunoglobulin, initial encounter" }, { "from_icd11": "NE60", "icd10_code": "T50Z95A", "icd10_title": "Adverse effect of other vaccines and biological substances, initial encounter" }, { "from_icd11": "NE60", "icd10_code": "T50A95S", "icd10_title": "Adverse effect of other bacterial vaccines, sequela" }, { "from_icd11": "NE60", "icd10_code": "T50B95A", "icd10_title": "Adverse effect of other viral vaccines, initial encounter" }, { "from_icd11": "NE60", "icd10_code": "T50A25A", "icd10_title": "Adverse effect of mixed bacterial vaccines without a pertussis component, initial encounter" }, { "from_icd11": "NE60", "icd10_code": "T50A91A", "icd10_title": "Poisoning by other bacterial vaccines, accidental (unintentional), initial encounter" } ]
K5900
Constipation, unspecified
A 10-year-old Saudi boy presented to the emergency department (A&E) of King Saud Hospital with complaints of fever, skin rash, and conjunctivitis of two days’ duration. He was well two days ago when he developed fever, which was intermittent initially and later became continuous; the fever was recorded up till 40 °C, relieved with antipyretic (acetaminophen) for a few hours before returning with rigors and chills. It was associated with generalized malaise and body aches. Skin rash appeared within 48 hours of onset of fever, on the face and then descended on the trunk and limbs. It was nonpruritic and without any skin bleed and was associated with mild swelling of hands, feet, and lips. He also developed redness of eyes but without watering, stickiness, or any pain on movement of eyeballs. There was a history of abdominal pain in the epigastrium and right hypochondrium with few grade III non-bloody stools. There was no associated history of photophobia, seizures, vomiting, pain abdomen, palpitations, breathing difficulty, joint pains or swelling, and urinary complaints or contact with any person with a similar illness at home. About four weeks ago, all family was diagnosed with PCR-positive COVID-19 infection after one of the parents developed symptoms of fever and body ache. No other family member developed any symptoms but they completed their isolation for 10 days. Repeat testing was not done.
3.628906
0.988281
sec[1]/p[0]
en
0.999996
PMC8826481
https://doi.org/10.7759/cureus.21064
[ "fever", "skin", "associated", "pain", "complaints", "rash", "hours", "body", "without", "swelling" ]
[ { "code": "MG26", "title": "Fever of other or unknown origin" }, { "code": "1D81.Z", "title": "Infectious mononucleosis, unspecified" }, { "code": "1B99", "title": "Pasteurellosis" }, { "code": "4A60.0", "title": "Familial Mediterranean fever" }, { "code": "JB40.0", "title": "Puerperal sepsis" }, { "code": "ME67", "title": "Skin disorder of uncertain or unspecified nature" }, { "code": "ME66.Y", "title": "Other specified skin changes" }, { "code": "EM0Y", "title": "Other specified diseases of the skin" }, { "code": "ME60.Z", "title": "Skin lesion of unspecified nature" }, { "code": "ME66.1", "title": "Changes in skin texture" } ]
=== ICD-11 CODES FOUND === [MG26] Fever of other or unknown origin Definition: An abnormal elevation of body temperature of unknown origin, often as a result of a pathologic process. Also known as: Fever of other or unknown origin | febrile | febris | fever | feverish Excludes: fever of unknown origin in newborn | Malignant hyperthermia due to anaesthesia [1D81.Z] Infectious mononucleosis, unspecified Also known as: Infectious mononucleosis, unspecified | Infectious mononucleosis | Glandular fever | Gammaherpesviral mononucleosis | kissing disease [1B99] Pasteurellosis Definition: A disease caused by an infection with the gram-negative bacteria Pasteurella. This disease is characterised by local cellulitis and may lead to other clinical signs depending on the route of infection. Transmission is commonly by direct contact through the bite, scratch, or lick from an infected animal, inhalation of infected respiratory secretions, or ingestion of contaminated meat. Confirmation is by identification of Pasteurella from the affected individual. Also known as: Pasteurellosis | pasteurella infection | shipping fever | transport fever [4A60.0] Familial Mediterranean fever Definition: FMF is an autoinflammatory disease associated with mutations in pyrin resulting in enhanced IL1 beta production. This results in clinical attacks of inflammation in the form of fever and serositis in the form of peritoneal, pleural or synovial inflammation along with increased acute phase reactants. Also known as: Familial Mediterranean fever | Periodic disease | FMF - [familial mediterranean fever] | periodic fever | periodic polyserositis [JB40.0] Puerperal sepsis Also known as: Puerperal sepsis | puerperal fever | postpartum sepsis | generalised puerperal infection | major puerperal infection Excludes: Obstetric pyaemic or septic embolism | sepsis during labour [ME67] Skin disorder of uncertain or unspecified nature Definition: A category to enable the presence of a skin disorder to be recorded without making assumptions as to the precise nature of the disorder in question. Also known as: Skin disorder of uncertain or unspecified nature | Skin disorder without established diagnosis | change of skin NOS | dermatological disease NOS | dermatological disorder NOS [ME66.Y] Other specified skin changes Also known as: Other specified skin changes | Cutis marmorata | Fear of skin disease | Retention hyperkeratosis | Dermatitis neglecta [EM0Y] Other specified diseases of the skin Also known as: Other specified diseases of the skin | Adverse cutaneous effects of healthcare related interventions | Cutaneous complications of surgical, laser or other interventional procedures | Postprocedural cutaneous complications of surgical, laser or other interventions | Cutaneous complications of surgical procedures [ME60.Z] Skin lesion of unspecified nature Also known as: Skin lesion of unspecified nature | Skin lesion of uncertain or unspecified nature | Skin lesion without established diagnosis | Pigmented skin lesion of unspecified nature | Ulcer of skin of unspecified nature [ME66.1] Changes in skin texture Definition: Alterations in skin texture of unspecified cause. Also known as: Changes in skin texture | Skin textural disturbance | Thickening of skin | induration of skin | Skin sclerosis === GRAPH WALKS === --- Walk 1 --- [MG26] Fever of other or unknown origin Def: An abnormal elevation of body temperature of unknown origin, often as a result of a pathologic process.... --EXCLUDES--> [?] Malignant hyperthermia due to anaesthesia Def: A condition caused by hypermetabolism in response to certain anaesthetic drugs. This condition is characterised by hyperthermia, tachycardia, tachypnoea, increased carbon dioxide production, increased... --PARENT--> [?] Other injury or harm from surgical or medical care, not elsewhere classified --- Walk 2 --- [MG26] Fever of other or unknown origin Def: An abnormal elevation of body temperature of unknown origin, often as a result of a pathologic process.... --RELATED_TO--> [?] Fever of newborn --PARENT--> [?] Fever of other or unknown origin Def: An abnormal elevation of body temperature of unknown origin, often as a result of a pathologic process.... --- Walk 3 --- [1D81.Z] Infectious mononucleosis, unspecified --PARENT--> [1D81] Infectious mononucleosis Def: A disease typically caused by an infection with Epstein-Barr virus or cytomegalovirus. This disease commonly presents with extreme fatigue, fever, acute pharyngitis, body aches, or lymphadenopathy. Tr... --CHILD--> [1D81.0] Mononucleosis due to Epstein-Barr virus Def: A disease typically caused by an infection with Epstein-Barr virus (EBV). This disease commonly presents with extreme fatigue, fever, acute pharyngitis, body aches, or lymphadenopathy. Transmission is... --- Walk 4 --- [1D81.Z] Infectious mononucleosis, unspecified --PARENT--> [1D81] Infectious mononucleosis Def: A disease typically caused by an infection with Epstein-Barr virus or cytomegalovirus. This disease commonly presents with extreme fatigue, fever, acute pharyngitis, body aches, or lymphadenopathy. Tr... --CHILD--> [1D81.1] Mononucleosis due to cytomegalovirus Def: A disease typically caused by an infection with cytomegalovirus. This disease commonly presents with extreme fatigue, fever, acute pharyngitis, body aches, or lymphadenopathy. Transmission is by direc... --- Walk 5 --- [1B99] Pasteurellosis Def: A disease caused by an infection with the gram-negative bacteria Pasteurella. This disease is characterised by local cellulitis and may lead to other clinical signs depending on the route of infection... --PARENT--> [?] Certain zoonotic bacterial diseases Def: This is a group of bacterial diseases that are transmitted to humans by contact with infected vertebrate animals.... --CHILD--> [1B90] Rat-bite fevers Def: Any disease caused by an infection with the gram-negative bacteria Streptobacillus moniliformis or gram-negative bacteria Spirillum minus. This disease presents with symptoms depending on the bacteria... --- Walk 6 --- [1B99] Pasteurellosis Def: A disease caused by an infection with the gram-negative bacteria Pasteurella. This disease is characterised by local cellulitis and may lead to other clinical signs depending on the route of infection... --PARENT--> [?] Certain zoonotic bacterial diseases Def: This is a group of bacterial diseases that are transmitted to humans by contact with infected vertebrate animals.... --CHILD--> [1B92] Glanders Def: A disease caused by an infection with the gram-negative bacteria Burkholderia mallei. This disease presents with symptoms depending on the route of infection. Transmission is by contact with tissues o...
[ "[MG26] Fever of other or unknown origin\n Def: An abnormal elevation of body temperature of unknown origin, often as a result of a pathologic process....\n --EXCLUDES--> [?] Malignant hyperthermia due to anaesthesia\n Def: A condition caused by hypermetabolism in response to certain anaesthetic drugs. This condition is characterised by hyperthermia, tachycardia, tachypnoea, increased carbon dioxide production, increased...\n --PARENT--> [?] Other injury or harm from surgical or medical care, not elsewhere classified", "[MG26] Fever of other or unknown origin\n Def: An abnormal elevation of body temperature of unknown origin, often as a result of a pathologic process....\n --RELATED_TO--> [?] Fever of newborn\n --PARENT--> [?] Fever of other or unknown origin\n Def: An abnormal elevation of body temperature of unknown origin, often as a result of a pathologic process....", "[1D81.Z] Infectious mononucleosis, unspecified\n --PARENT--> [1D81] Infectious mononucleosis\n Def: A disease typically caused by an infection with Epstein-Barr virus or cytomegalovirus. This disease commonly presents with extreme fatigue, fever, acute pharyngitis, body aches, or lymphadenopathy. Tr...\n --CHILD--> [1D81.0] Mononucleosis due to Epstein-Barr virus\n Def: A disease typically caused by an infection with Epstein-Barr virus (EBV). This disease commonly presents with extreme fatigue, fever, acute pharyngitis, body aches, or lymphadenopathy. Transmission is...", "[1D81.Z] Infectious mononucleosis, unspecified\n --PARENT--> [1D81] Infectious mononucleosis\n Def: A disease typically caused by an infection with Epstein-Barr virus or cytomegalovirus. This disease commonly presents with extreme fatigue, fever, acute pharyngitis, body aches, or lymphadenopathy. Tr...\n --CHILD--> [1D81.1] Mononucleosis due to cytomegalovirus\n Def: A disease typically caused by an infection with cytomegalovirus. This disease commonly presents with extreme fatigue, fever, acute pharyngitis, body aches, or lymphadenopathy. Transmission is by direc...", "[1B99] Pasteurellosis\n Def: A disease caused by an infection with the gram-negative bacteria Pasteurella. This disease is characterised by local cellulitis and may lead to other clinical signs depending on the route of infection...\n --PARENT--> [?] Certain zoonotic bacterial diseases\n Def: This is a group of bacterial diseases that are transmitted to humans by contact with infected vertebrate animals....\n --CHILD--> [1B90] Rat-bite fevers\n Def: Any disease caused by an infection with the gram-negative bacteria Streptobacillus moniliformis or gram-negative bacteria Spirillum minus. This disease presents with symptoms depending on the bacteria...", "[1B99] Pasteurellosis\n Def: A disease caused by an infection with the gram-negative bacteria Pasteurella. This disease is characterised by local cellulitis and may lead to other clinical signs depending on the route of infection...\n --PARENT--> [?] Certain zoonotic bacterial diseases\n Def: This is a group of bacterial diseases that are transmitted to humans by contact with infected vertebrate animals....\n --CHILD--> [1B92] Glanders\n Def: A disease caused by an infection with the gram-negative bacteria Burkholderia mallei. This disease presents with symptoms depending on the route of infection. Transmission is by contact with tissues o..." ]
MG26
Fever of other or unknown origin
[ { "from_icd11": "MG26", "icd10_code": "R5081", "icd10_title": "Fever presenting with conditions classified elsewhere" }, { "from_icd11": "MG26", "icd10_code": "R5084", "icd10_title": "Febrile nonhemolytic transfusion reaction" }, { "from_icd11": "MG26", "icd10_code": "R5082", "icd10_title": "Postprocedural fever" }, { "from_icd11": "MG26", "icd10_code": "R5083", "icd10_title": "Postvaccination fever" }, { "from_icd11": "MG26", "icd10_code": "R509", "icd10_title": "Fever, unspecified" }, { "from_icd11": "MG26", "icd10_code": "R502", "icd10_title": "Drug induced fever" }, { "from_icd11": "MG26", "icd10_code": "R50", "icd10_title": "Fever of other and unknown origin" }, { "from_icd11": "MG26", "icd10_code": "R508", "icd10_title": "Other specified fever" }, { "from_icd11": "1D81.Z", "icd10_code": "B2700", "icd10_title": "Gammaherpesviral mononucleosis without complication" }, { "from_icd11": "1D81.Z", "icd10_code": "B2790", "icd10_title": "Infectious mononucleosis, unspecified without complication" }, { "from_icd11": "1D81.Z", "icd10_code": "B2709", "icd10_title": "Gammaherpesviral mononucleosis with other complications" }, { "from_icd11": "1D81.Z", "icd10_code": "B2780", "icd10_title": "Other infectious mononucleosis without complication" }, { "from_icd11": "1D81.Z", "icd10_code": "B2799", "icd10_title": "Infectious mononucleosis, unspecified with other complication" }, { "from_icd11": "1D81.Z", "icd10_code": "B2701", "icd10_title": "Gammaherpesviral mononucleosis with polyneuropathy" }, { "from_icd11": "1D81.Z", "icd10_code": "B2789", "icd10_title": "Other infectious mononucleosis with other complication" } ]
R5081
Fever presenting with conditions classified elsewhere
Multiple adhesions were seen over the omentum, intestines, and uterus. The uterovesical fold was separated and the bladder was pushed down. Resection of the margins of the ovarian mass was performed systematically using a clamp, cut, ligate technique and cautery. The right round ligament was clamped cut and transfixed. The right fallopian tube along with the ovarian mass was removed and sent for histopathological examination (HPE) and frozen biopsy. Tissue noted to be adhered to the posterior wall of the uterus was resected gently using cautery and saline irrigation. Uterus left intact in situ, noted to be hypoplastic. The left ovarian margin cleared and the left ovary was left intact in situ. The left round ligament was clamped cut and transfixed. The left-sided fallopian tube was removed and sent for HPE. The contralateral fallopian tube was removed as it was badly adhered to the posterior surface of the uterus. Intraoperative surgical assistance for dissection between the sigmoid colon and the tumor was done by the surgeon. Three serosal tears of 1×1 cm were noted that were sutured back using vicryl 3-0. Hemostasis was achieved. The frozen section report confirmed germ cell tumor diagnosis consisting of YST of stage III A1 according to the International Federation of Gynaecology and Obstetrics staging as illustrated in Figure 3 . Based on the report, the decision for further staging was taken.
3.882813
0.972168
sec[1]/p[8]
en
0.999997
PMC11549645
https://doi.org/10.7759/cureus.71184
[ "uterus", "ovarian", "using", "fallopian", "tube", "cautery", "round", "ligament", "clamped", "transfixed" ]
[ { "code": "GA1Z&XA99N3", "title": "Noninflammatory disorders of uterus, except cervix" }, { "code": "GA01.Z", "title": "Inflammatory disorders of the uterus, except cervix, unspecified" }, { "code": "GA16.Y", "title": "Other specified acquired abnormalities of uterus, except cervix" }, { "code": "NB92.6", "title": "Injury of uterus" }, { "code": "GC04.1Y", "title": "Other specified fistulae involving female genital tract" }, { "code": "GA1Z&XA1QK0", "title": "Noninflammatory disorders of ovary" }, { "code": "GA07.Z&XA1QK0", "title": "Inflammation of ovary" }, { "code": "GA30.6", "title": "Premature ovarian failure" }, { "code": "JA01.2", "title": "Ovarian pregnancy" }, { "code": "QF01.10", "title": "Acquired absence of female genital organs" } ]
=== ICD-11 CODES FOUND === [GA01.Z] Inflammatory disorders of the uterus, except cervix, unspecified Also known as: Inflammatory disorders of the uterus, except cervix, unspecified | Inflammatory disorders of the uterus, except cervix | inflammatory disease of the uterus | uterine inflammatory disease | uterus inflammation [GA16.Y] Other specified acquired abnormalities of uterus, except cervix Also known as: Other specified acquired abnormalities of uterus, except cervix | Polyp of corpus uteri | intrauterine polyp | polyp of body of uterus | polyp of uterus [NB92.6] Injury of uterus Also known as: Injury of uterus | uterine injury | intrauterine injury NOS | Injury of uterus without open wound into cavity | Injury of uterus with open wound into cavity [GC04.1Y] Other specified fistulae involving female genital tract Also known as: Other specified fistulae involving female genital tract | Other female intestinal-genital tract fistulae | Intestinouterine fistula | enterouterine fistula | Cervicosigmoidal fistula [GA30.6] Premature ovarian failure Definition: Menopause occurring spontaneously before 40 years of age, generally resulting in secondary amenorrhea although some women may exhibit intermittent ovarian function and ovulation, with a minority conceiving and delivering a pregnancy. POF/POI occurs mostly without a known cause, but can be caused by the following conditions: numerical and structural chromosomal abnormalities, Fragile X (FMR1) premutations, autoimmune disorders, radiation therapy, chemotherapy, galactosemia, and other rare enzyme Also known as: Premature ovarian failure | female hypergonadotropic hypogonadism | hypergonadotrophic ovarian failure | primary female hypogonadism | POF - [premature ovarian failure] Excludes: Isolated gonadotropin deficiency | Postprocedural ovarian failure [JA01.2] Ovarian pregnancy Definition: A condition characterised by implantation of the embryo within the ovary during pregnancy. Also known as: Ovarian pregnancy [QF01.10] Acquired absence of female genital organs Also known as: Acquired absence of female genital organs | Acquired absence of cervix | amputation of cervix | Acquired absence of the uterus | acquired uterine absence === GRAPH WALKS === --- Walk 1 --- [GA01.Z] Inflammatory disorders of the uterus, except cervix, unspecified --PARENT--> [GA01] Inflammatory disorders of the uterus, except cervix Def: A spectrum of inflammations involving the Uterus and the supporting tissues. It is usually caused by an ascending infection of organisms from the endocervix. Such inflammation can lead to functional i... --CHILD--> [GA01.Y] Other specified inflammatory disorders of the uterus, except cervix --- Walk 2 --- [GA01.Z] Inflammatory disorders of the uterus, except cervix, unspecified --PARENT--> [GA01] Inflammatory disorders of the uterus, except cervix Def: A spectrum of inflammations involving the Uterus and the supporting tissues. It is usually caused by an ascending infection of organisms from the endocervix. Such inflammation can lead to functional i... --CHILD--> [GA01.0] Acute inflammatory disease of uterus --- Walk 3 --- [GA16.Y] Other specified acquired abnormalities of uterus, except cervix --PARENT--> [GA16] Acquired abnormalities of uterus, except cervix Def: Any condition of the uterus, caused by determinants arising after birth. These conditions are characterised by a malfunction, malformation, or another anomaly of the uterus (excluding the cervix).... --RELATED_TO--> [?] Adenomyosis Def: A condition of the uterus characterised by endometrial tissue growth in the myometrium, hypertrophy of the myometrium, and heavy or prolonged menstrual bleeding, dysmenorrhoea, dyspareunia, bleeding b... --- Walk 4 --- [GA16.Y] Other specified acquired abnormalities of uterus, except cervix --PARENT--> [GA16] Acquired abnormalities of uterus, except cervix Def: Any condition of the uterus, caused by determinants arising after birth. These conditions are characterised by a malfunction, malformation, or another anomaly of the uterus (excluding the cervix).... --CHILD--> [GA16.0] Endometrial glandular hyperplasia Def: A condition of the uterus, caused by chronic, excess oestrogen stimulation due to obesity, anovulation, or oestrogen therapy. This condition is characterised by excessive proliferation of the endometr... --- Walk 5 --- [NB92.6] Injury of uterus --PARENT--> [NB92] Injury of urinary or pelvic organs --CHILD--> [NB92.2] Injury of bladder --- Walk 6 --- [NB92.6] Injury of uterus --PARENT--> [NB92] Injury of urinary or pelvic organs --CHILD--> [NB92.0] Injury of kidney
[ "[GA01.Z] Inflammatory disorders of the uterus, except cervix, unspecified\n --PARENT--> [GA01] Inflammatory disorders of the uterus, except cervix\n Def: A spectrum of inflammations involving the Uterus and the supporting tissues. It is usually caused by an ascending infection of organisms from the endocervix. Such inflammation can lead to functional i...\n --CHILD--> [GA01.Y] Other specified inflammatory disorders of the uterus, except cervix", "[GA01.Z] Inflammatory disorders of the uterus, except cervix, unspecified\n --PARENT--> [GA01] Inflammatory disorders of the uterus, except cervix\n Def: A spectrum of inflammations involving the Uterus and the supporting tissues. It is usually caused by an ascending infection of organisms from the endocervix. Such inflammation can lead to functional i...\n --CHILD--> [GA01.0] Acute inflammatory disease of uterus", "[GA16.Y] Other specified acquired abnormalities of uterus, except cervix\n --PARENT--> [GA16] Acquired abnormalities of uterus, except cervix\n Def: Any condition of the uterus, caused by determinants arising after birth. These conditions are characterised by a malfunction, malformation, or another anomaly of the uterus (excluding the cervix)....\n --RELATED_TO--> [?] Adenomyosis\n Def: A condition of the uterus characterised by endometrial tissue growth in the myometrium, hypertrophy of the myometrium, and heavy or prolonged menstrual bleeding, dysmenorrhoea, dyspareunia, bleeding b...", "[GA16.Y] Other specified acquired abnormalities of uterus, except cervix\n --PARENT--> [GA16] Acquired abnormalities of uterus, except cervix\n Def: Any condition of the uterus, caused by determinants arising after birth. These conditions are characterised by a malfunction, malformation, or another anomaly of the uterus (excluding the cervix)....\n --CHILD--> [GA16.0] Endometrial glandular hyperplasia\n Def: A condition of the uterus, caused by chronic, excess oestrogen stimulation due to obesity, anovulation, or oestrogen therapy. This condition is characterised by excessive proliferation of the endometr...", "[NB92.6] Injury of uterus\n --PARENT--> [NB92] Injury of urinary or pelvic organs\n --CHILD--> [NB92.2] Injury of bladder", "[NB92.6] Injury of uterus\n --PARENT--> [NB92] Injury of urinary or pelvic organs\n --CHILD--> [NB92.0] Injury of kidney" ]
GA1Z&XA99N3
Noninflammatory disorders of uterus, except cervix
[ { "from_icd11": "GA01.Z", "icd10_code": "N719", "icd10_title": "Inflammatory disease of uterus, unspecified" }, { "from_icd11": "GA01.Z", "icd10_code": "N71", "icd10_title": "Inflammatory disease of uterus, except cervix" }, { "from_icd11": "NB92.6", "icd10_code": "S3763XA", "icd10_title": "Laceration of uterus, initial encounter" }, { "from_icd11": "NB92.6", "icd10_code": "S3769XA", "icd10_title": "Other injury of uterus, initial encounter" }, { "from_icd11": "NB92.6", "icd10_code": "S3760XA", "icd10_title": "Unspecified injury of uterus, initial encounter" }, { "from_icd11": "NB92.6", "icd10_code": "S376", "icd10_title": "Injury of uterus" }, { "from_icd11": "GA30.6", "icd10_code": "E2839", "icd10_title": "Other primary ovarian failure" }, { "from_icd11": "GA30.6", "icd10_code": "E28319", "icd10_title": "Asymptomatic premature menopause" }, { "from_icd11": "GA30.6", "icd10_code": "E28310", "icd10_title": "Symptomatic premature menopause" }, { "from_icd11": "GA30.6", "icd10_code": "E283", "icd10_title": "Primary ovarian failure" }, { "from_icd11": "JA01.2", "icd10_code": "O00201", "icd10_title": "Right ovarian pregnancy without intrauterine pregnancy" }, { "from_icd11": "JA01.2", "icd10_code": "O002", "icd10_title": "Ovarian pregnancy" } ]
N719
Inflammatory disease of uterus, unspecified
After the surgery, the patient was transferred to the intensive care unit (ICU) with artificial respiration, and dexmedetomidine 0.43 μg/kg/h and fentanyl 30 μg/h were administered for sedation and analgesia. On the first postoperative day (POD 1), an extreme elevation of creatine kinase (CK, 3,730 U/L) and a 39 °C fever of uncertain etiology were observed. We suspected propofol infusion syndrome (PRIS), malignant hyperthermia (MH), neuroleptic malignant syndrome, drug-induced rhabdomyolysis, and/or serotonin syndrome; therefore, we ceased administration of any potentially related drugs (propofol, piperacillin/tazobactam, fentanyl) and started administration of midazolam and dexmedetomidine instead. Although the CK value peaked at 45,288 U/L on POD 7 after gradual increase from POD 1, it was decreased after POD 8 due to the dantrolene 40 mg administrated on POD 7. In addition, a decrease in renal function (estimated glomerular filtration rate: 17.6 mL/min/1.73 m 2 ) was observed postoperatively; thus, continuous hemodiafiltration (CHDF) was performed from POD 2. Moreover, mechanical ventilation had been continued because of poor oxygenation due to pneumonia since surgery. We did not perform tracheostomy because of the high possibility of mediastinitis due to the protruding sternal wires and possible difficulty of hemostasis by anticoagulants for CHDF, in spite of long-term mechanical ventilation.
3.943359
0.963867
sec[1]/p[1]
en
0.999997
33011931
https://doi.org/10.1186/s40981-020-00382-z
[ "dexmedetomidine", "fentanyl", "propofol", "malignant", "administration", "chdf", "mechanical", "ventilation", "because", "transferred" ]
[ { "code": "NE60", "title": "Harmful effects of drugs, medicaments or biological substances, not elsewhere classified" }, { "code": "6C43.3", "title": "Opioid intoxication" }, { "code": "6C4F.3", "title": "Intoxication due to multiple specified psychoactive substances" }, { "code": "PB20&XM76M8", "title": "Accidental fentanyl poisoning" }, { "code": "PH40", "title": "Exposure to or harmful effects of undetermined intent of opioids or related analgesics" }, { "code": "2D4Z", "title": "Unspecified malignant neoplasms of unspecified sites" }, { "code": "2E2Z", "title": "Malignant neoplasm metastasis, unspecified" }, { "code": "2B70.Z", "title": "Malignant neoplasms of oesophagus, unspecified" }, { "code": "2B33.Y", "title": "Other malignant haematopoietic neoplasms without further specification" }, { "code": "2B31.1", "title": "Histiocytic sarcoma" } ]
=== ICD-11 CODES FOUND === [NE60] Harmful effects of drugs, medicaments or biological substances, not elsewhere classified Also known as: Harmful effects of drugs, medicaments or biological substances, not elsewhere classified | drugs, medicaments or biological substances, toxicity not elsewhere classified | adverse drug effects | drug reaction NOS | drug allergy NOS Excludes: Alcohol intoxication | pathological drug intoxication | hypersensitivity reaction to correctly administered drug [6C43.3] Opioid intoxication Definition: Opioid intoxication is a clinically significant transient condition that develops during or shortly after the consumption of opioids that is characterised by disturbances in consciousness, cognition, perception, affect, behaviour, or coordination. These disturbances are caused by the known pharmacological effects of opioids and their intensity is closely related to the amount of opioids consumed. They are time-limited and abate as opioids are cleared from the body. Presenting features may includ Also known as: Opioid intoxication | heroin intoxication | bad trip due to opioids | Acute intoxication due to fentanyl | Fentanyl and despropionyl fentanyl intoxication Excludes: opioid poisoning | Possession trance disorder | fentanyl poisoning [6C4F.3] Intoxication due to multiple specified psychoactive substances Definition: Intoxication due to multiple specified psychoactive substances is a clinically significant transient condition that develops during or shortly after the consumption of multiple specified substances or medications that is characterised by disturbances in consciousness, cognition, perception, affect, behaviour, or coordination. These disturbances are caused by the known pharmacological effects of the multiple specified psychoactive substances and their intensity is closely related to the amount of Also known as: Intoxication due to multiple specified psychoactive substances | mixed drug intoxication NOS | combined drug intoxication NOS | acute mixed drug intoxication NOS | acute combined drug intoxication NOS [PH40] Exposure to or harmful effects of undetermined intent of opioids or related analgesics Also known as: Exposure to or harmful effects of undetermined intent of opioids or related analgesics | Harmful effects of or exposure to opium, undetermined intent | Harmful effects of or exposure to morphine, undetermined intent | Harmful effects of or exposure to oxycodone, undetermined intent | Harmful effects of or exposure to codeine, undetermined intent [2D4Z] Unspecified malignant neoplasms of unspecified sites Also known as: Unspecified malignant neoplasms of unspecified sites | malignancy of unspecified site | malignancy unspecified primary site | malignant growth of unspecified site | malignant mass of unspecified site [2E2Z] Malignant neoplasm metastasis, unspecified Also known as: Malignant neoplasm metastasis, unspecified | secondary malignant neoplasm | metastasis | metastases | disseminated metastases [2B70.Z] Malignant neoplasms of oesophagus, unspecified Also known as: Malignant neoplasms of oesophagus, unspecified | Malignant neoplasms of oesophagus | cancer of oesophagus | oesophageal malignancy | oesophageal cancer [2B33.Y] Other malignant haematopoietic neoplasms without further specification Also known as: Other malignant haematopoietic neoplasms without further specification | Malignant neoplasm blood other | Haematological malignancy NOS | Neoplasm blood benign or unspecified [2B31.1] Histiocytic sarcoma Also known as: Histiocytic sarcoma | Malignant Histiocytosis Includes: Malignant Histiocytosis === GRAPH WALKS === --- Walk 1 --- [NE60] Harmful effects of drugs, medicaments or biological substances, not elsewhere classified --EXCLUDES--> [?] Alcohol intoxication Def: Alcohol intoxication is a clinically significant transient condition that develops during or shortly after the consumption of alcohol that is characterised by disturbances in consciousness, cognition,... --EXCLUDES--> [?] Harmful effects of or exposure to noxious substances chiefly nonmedicinal as to source, alcohols --- Walk 2 --- [NE60] Harmful effects of drugs, medicaments or biological substances, not elsewhere classified --EXCLUDES--> [?] Allergic or hypersensitivity conditions Def: Allergy is a hypersensitivity reaction initiated by proven immunologic mechanisms. Hypersensitivity is defined as conditions clinically resembling allergy that cause objectively reproducible symptoms... --CHILD--> [?] Allergic or hypersensitivity disorders involving skin or mucous membranes Def: Allergic or hypersensitivity disorders involving the skin and mucous includes a heterogeneous group of disorders involving skin and mucous membranes in which either allergy or hypersensitivity play a ... --- Walk 3 --- [6C43.3] Opioid intoxication Def: Opioid intoxication is a clinically significant transient condition that develops during or shortly after the consumption of opioids that is characterised by disturbances in consciousness, cognition, ... --EXCLUDES--> [?] Harmful effects of opioids or related analgesics --CHILD--> [?] Harmful effects of oxycodone --- Walk 4 --- [6C43.3] Opioid intoxication Def: Opioid intoxication is a clinically significant transient condition that develops during or shortly after the consumption of opioids that is characterised by disturbances in consciousness, cognition, ... --PARENT--> [6C43] Disorders due to use of opioids Def: Disorders due to use of opioids are characterised by the pattern and consequences of opioid use. Opioids is a generic term that encompasses the constituents or derivatives of the opium poppy Papaver s... --CHILD--> [6C43.2] Opioid dependence Def: Opioid dependence is a disorder of regulation of opioid use arising from repeated or continuous use of opioids. The characteristic feature is a strong internal drive to use opioids, which is manifeste... --- Walk 5 --- [6C4F.3] Intoxication due to multiple specified psychoactive substances Def: Intoxication due to multiple specified psychoactive substances is a clinically significant transient condition that develops during or shortly after the consumption of multiple specified substances or... --PARENT--> [6C4F] Disorders due to use of multiple specified psychoactive substances, including medications Def: Disorders due to use of multiple specified psychoactive substances, including medications are characterised by the pattern and consequences of multiple psychoactive substances. Although this grouping ... --CHILD--> [6C4F.2] Multiple specified psychoactive substances dependence Def: Multiple specified psychoactive substance dependence is a disorder of regulation of use of multiple specified substances arising from repeated or continuous use of the specified substances. The charac... --- Walk 6 --- [6C4F.3] Intoxication due to multiple specified psychoactive substances Def: Intoxication due to multiple specified psychoactive substances is a clinically significant transient condition that develops during or shortly after the consumption of multiple specified substances or... --PARENT--> [6C4F] Disorders due to use of multiple specified psychoactive substances, including medications Def: Disorders due to use of multiple specified psychoactive substances, including medications are characterised by the pattern and consequences of multiple psychoactive substances. Although this grouping ... --CHILD--> [6C4F.2] Multiple specified psychoactive substances dependence Def: Multiple specified psychoactive substance dependence is a disorder of regulation of use of multiple specified substances arising from repeated or continuous use of the specified substances. The charac...
[ "[NE60] Harmful effects of drugs, medicaments or biological substances, not elsewhere classified\n --EXCLUDES--> [?] Alcohol intoxication\n Def: Alcohol intoxication is a clinically significant transient condition that develops during or shortly after the consumption of alcohol that is characterised by disturbances in consciousness, cognition,...\n --EXCLUDES--> [?] Harmful effects of or exposure to noxious substances chiefly nonmedicinal as to source, alcohols", "[NE60] Harmful effects of drugs, medicaments or biological substances, not elsewhere classified\n --EXCLUDES--> [?] Allergic or hypersensitivity conditions\n Def: Allergy is a hypersensitivity reaction initiated by proven immunologic mechanisms.\n\nHypersensitivity is defined as conditions clinically resembling allergy that cause objectively reproducible symptoms...\n --CHILD--> [?] Allergic or hypersensitivity disorders involving skin or mucous membranes\n Def: Allergic or hypersensitivity disorders involving the skin and mucous includes a heterogeneous group of disorders involving skin and mucous membranes in which either allergy or hypersensitivity play a ...", "[6C43.3] Opioid intoxication\n Def: Opioid intoxication is a clinically significant transient condition that develops during or shortly after the consumption of opioids that is characterised by disturbances in consciousness, cognition, ...\n --EXCLUDES--> [?] Harmful effects of opioids or related analgesics\n --CHILD--> [?] Harmful effects of oxycodone", "[6C43.3] Opioid intoxication\n Def: Opioid intoxication is a clinically significant transient condition that develops during or shortly after the consumption of opioids that is characterised by disturbances in consciousness, cognition, ...\n --PARENT--> [6C43] Disorders due to use of opioids\n Def: Disorders due to use of opioids are characterised by the pattern and consequences of opioid use. Opioids is a generic term that encompasses the constituents or derivatives of the opium poppy Papaver s...\n --CHILD--> [6C43.2] Opioid dependence\n Def: Opioid dependence is a disorder of regulation of opioid use arising from repeated or continuous use of opioids. The characteristic feature is a strong internal drive to use opioids, which is manifeste...", "[6C4F.3] Intoxication due to multiple specified psychoactive substances\n Def: Intoxication due to multiple specified psychoactive substances is a clinically significant transient condition that develops during or shortly after the consumption of multiple specified substances or...\n --PARENT--> [6C4F] Disorders due to use of multiple specified psychoactive substances, including medications\n Def: Disorders due to use of multiple specified psychoactive substances, including medications are characterised by the pattern and consequences of multiple psychoactive substances. Although this grouping ...\n --CHILD--> [6C4F.2] Multiple specified psychoactive substances dependence\n Def: Multiple specified psychoactive substance dependence is a disorder of regulation of use of multiple specified substances arising from repeated or continuous use of the specified substances. The charac...", "[6C4F.3] Intoxication due to multiple specified psychoactive substances\n Def: Intoxication due to multiple specified psychoactive substances is a clinically significant transient condition that develops during or shortly after the consumption of multiple specified substances or...\n --PARENT--> [6C4F] Disorders due to use of multiple specified psychoactive substances, including medications\n Def: Disorders due to use of multiple specified psychoactive substances, including medications are characterised by the pattern and consequences of multiple psychoactive substances. Although this grouping ...\n --CHILD--> [6C4F.2] Multiple specified psychoactive substances dependence\n Def: Multiple specified psychoactive substance dependence is a disorder of regulation of use of multiple specified substances arising from repeated or continuous use of the specified substances. The charac..." ]
NE60
Harmful effects of drugs, medicaments or biological substances, not elsewhere classified
[ { "from_icd11": "NE60", "icd10_code": "T50A95A", "icd10_title": "Adverse effect of other bacterial vaccines, initial encounter" }, { "from_icd11": "NE60", "icd10_code": "T50Z15A", "icd10_title": "Adverse effect of immunoglobulin, initial encounter" }, { "from_icd11": "NE60", "icd10_code": "T50Z95A", "icd10_title": "Adverse effect of other vaccines and biological substances, initial encounter" }, { "from_icd11": "NE60", "icd10_code": "T50A95S", "icd10_title": "Adverse effect of other bacterial vaccines, sequela" }, { "from_icd11": "NE60", "icd10_code": "T50B95A", "icd10_title": "Adverse effect of other viral vaccines, initial encounter" }, { "from_icd11": "NE60", "icd10_code": "T50A25A", "icd10_title": "Adverse effect of mixed bacterial vaccines without a pertussis component, initial encounter" }, { "from_icd11": "NE60", "icd10_code": "T50A91A", "icd10_title": "Poisoning by other bacterial vaccines, accidental (unintentional), initial encounter" }, { "from_icd11": "NE60", "icd10_code": "T498X5A", "icd10_title": "Adverse effect of other topical agents, initial encounter" }, { "from_icd11": "NE60", "icd10_code": "T48905A", "icd10_title": "Adverse effect of unspecified agents primarily acting on the respiratory system, initial encounter" }, { "from_icd11": "NE60", "icd10_code": "T48995A", "icd10_title": "Adverse effect of other agents primarily acting on the respiratory system, initial encounter" }, { "from_icd11": "NE60", "icd10_code": "T50A15A", "icd10_title": "Adverse effect of pertussis vaccine, including combinations with a pertussis component, initial encounter" }, { "from_icd11": "NE60", "icd10_code": "T50B15A", "icd10_title": "Adverse effect of smallpox vaccines, initial encounter" }, { "from_icd11": "NE60", "icd10_code": "T416X3A", "icd10_title": "" }, { "from_icd11": "NE60", "icd10_code": "T419X3A", "icd10_title": "" }, { "from_icd11": "NE60", "icd10_code": "T418X2A", "icd10_title": "" } ]
T50A95A
Adverse effect of other bacterial vaccines, initial encounter
Patient P04 is a 36-year-old male. Fundus images show extensive intraretinal pigment migrations extending from the mid-periphery equatorial region to the arcades in both eyes with extensive arterial attenuation, macular and peripapillary atrophy, only central 1 PD foveal island was sparing . OCT images show high-density deposits on the surface of RPE layer in macula, residual intraretinal vacuoles and an entirely disrupted and atrophy of the retina and macula, the outer retinal structures are lost . Fluorescein angiography show heterogeneous hyperautofluorescence with hypoautofluorescent fovea compatible with retinal atrophy . The full-field ERG shows a decrease in rod and cone amplitudes in rod response and combined rod-cone response, as well as a delayed implicit time. The 30 Hz Flicker cone response also shows a decreased amplitude . Several variants were identified in patient P04: one known variant in OPTN that was previously reported as benign, and two additional variants in PDE6A . The novel variant was predicted by most of the online prediction programs as damaging (Table 1 ) and was not reported previously in the gnomAD database. The two PDE6A variants are located on different alleles, as can be concluded from the genotype of III1 . Those findings indicate that the variants identified in PDE6A are the cause of the disease. Fig. 4 Clinical observations and identification of variants in P04
4.105469
0.503906
sec[2]/p[7]
en
0.999996
35033039
https://doi.org/10.1186/s12886-021-02242-5
[ "variants", "atrophy", "cone", "response", "intraretinal", "macula", "retinal", "variant", "that", "previously" ]
[ { "code": "4A00.0Y", "title": "Other specified functional neutrophil defects" }, { "code": "8A40.Y", "title": "Other specified multiple sclerosis" }, { "code": "8E4A.0", "title": "Paraneoplastic or autoimmune disorders of the central nervous system, brain or spinal cord" }, { "code": "8E01.2", "title": "Variant Creutzfeldt-Jakob Disease" }, { "code": "5C56.00", "title": "Gangliosidosis" }, { "code": "FB32.Y", "title": "Other specified disorders of muscles" }, { "code": "BE2Y", "title": "Other specified diseases of the circulatory system" }, { "code": "CB40.Y", "title": "Other specified diseases of the respiratory system" }, { "code": "9C40.BZ", "title": "Optic atrophy, unspecified" }, { "code": "8E7Y", "title": "Other specified diseases of the nervous system" } ]
=== ICD-11 CODES FOUND === [4A00.0Y] Other specified functional neutrophil defects Also known as: Other specified functional neutrophil defects | Chronic granulomatous disease | Chronic septic granulomatosis | CGD - [chronic granulomatous disease] | chronic granulomatous disorder [8A40.Y] Other specified multiple sclerosis Also known as: Other specified multiple sclerosis | Certain specified rare variants of multiple sclerosis | Multiple sclerosis, Marburg variant | Myelinoclastic diffuse sclerosis | Schilder disease [8E4A.0] Paraneoplastic or autoimmune disorders of the central nervous system, brain or spinal cord Definition: Paraneoplastic and autoimmune disorders of the central nervous system, brain and spinal cord nervous system result from a targeted immune attack on neurons or glial cells in the central (e.g. encephalopathy, ataxia, myelopathy, myelitis) nervous system. In the paraneoplastic context, this attack is a consequence of a potentially effective tumour immune response initiated by onco-neural antigens derived from a systemic cancer. In the non-paraneoplastic context termed ‘autoimmune’ the etiology rem Also known as: Paraneoplastic or autoimmune disorders of the central nervous system, brain or spinal cord | Paraneoplastic encephalitis | Paraneoplastic encephalitis, neural autoantibody positive | Paraneoplastic encephalitis, neural autoantibody negative | Autoimmune encephalitis [8E01.2] Variant Creutzfeldt-Jakob Disease Definition: A disease of the brain, that is suspected to be caused by a prion associated with Bovine Spongiform Encephalopathy. This disease is characterised by a long incubation period, psychiatric symptoms followed by neurological deficits, and is fatal. Transmission may be by ingestion of food (with a bovine origin) contaminated with infected brain or spinal cord from an infected cow, or blood transfusion. Confirmation is by pathological examination of the brain. Also known as: Variant Creutzfeldt-Jakob Disease | vCJD - [Variant Creutzfeldt-Jakob Disease] [5C56.00] Gangliosidosis Also known as: Gangliosidosis | GM1 gangliosidosis | Landing disease | GM1 gangliosidosis type 1 | Generalised gangliosidosis [FB32.Y] Other specified disorders of muscles Also known as: Other specified disorders of muscles | Muscle wasting or atrophy, not elsewhere classified | muscle wasting | muscle wasting disorder | Sarcopenia [BE2Y] Other specified diseases of the circulatory system Also known as: Other specified diseases of the circulatory system | Certain specified forms of heart disease | Cardiac disorder, unspecified | disorder of heart NOS | organic disease or disorder of heart [CB40.Y] Other specified diseases of the respiratory system Also known as: Other specified diseases of the respiratory system | Secondary respiratory disorders | Respiratory disorders in diseases classified elsewhere | Diseases of bronchus, not elsewhere classified | Acquired bronchial diverticulum [9C40.BZ] Optic atrophy, unspecified Also known as: Optic atrophy, unspecified | Optic atrophy | optic nerve atrophy | Primary optic atrophy | OA - [optic atrophy] [8E7Y] Other specified diseases of the nervous system Also known as: Other specified diseases of the nervous system | Circumscribed brain atrophy | circumscribed cerebral atrophy | atrophic lobar sclerosis | atrophic lobar brain sclerosis === GRAPH WALKS === --- Walk 1 --- [4A00.0Y] Other specified functional neutrophil defects --PARENT--> [4A00.0] Functional neutrophil defects --CHILD--> [4A00.0Y] Other specified functional neutrophil defects --- Walk 2 --- [4A00.0Y] Other specified functional neutrophil defects --PARENT--> [4A00.0] Functional neutrophil defects --CHILD--> [4A00.00] Neutrophil immunodeficiency syndrome Def: Neutrophil immunodeficiency syndrome is a primary immunodeficiency characterised by neutrophilia with severe neutrophil dysfunction, leukocytosis, a predisposition to bacterial infections and poor wou... --- Walk 3 --- [8A40.Y] Other specified multiple sclerosis --PARENT--> [8A40] Multiple sclerosis Def: Multiple Sclerosis (MS) is a chronic, inflammatory demyelinating disease of the central nervous system. Three categories of multiple sclerosis have been outlined: Relapsing/remitting, secondary progre... --CHILD--> [8A40.0] Relapsing-remitting multiple sclerosis Def: Clearly defined disease relapses with full recovery or with sequelae and residual deficit upon recovery. The periods between disease relapses are characterised by a lack of disease progression.... --- Walk 4 --- [8A40.Y] Other specified multiple sclerosis --PARENT--> [8A40] Multiple sclerosis Def: Multiple Sclerosis (MS) is a chronic, inflammatory demyelinating disease of the central nervous system. Three categories of multiple sclerosis have been outlined: Relapsing/remitting, secondary progre... --CHILD--> [8A40.2] Secondary progressive multiple sclerosis --- Walk 5 --- [8E4A.0] Paraneoplastic or autoimmune disorders of the central nervous system, brain or spinal cord Def: Paraneoplastic and autoimmune disorders of the central nervous system, brain and spinal cord nervous system result from a targeted immune attack on neurons or glial cells in the central (e.g. encephal... --PARENT--> [8E4A] Paraneoplastic or autoimmune disorders of the nervous system Def: Paraneoplastic and autoimmune disorders of the nervous system result from a targeted immune attack on neurons or glial cells in the central (e.g. encephalopathy, ataxia, myelitis) or peripheral nervou... --PARENT--> [?] Certain disorders of the nervous system --- Walk 6 --- [8E4A.0] Paraneoplastic or autoimmune disorders of the central nervous system, brain or spinal cord Def: Paraneoplastic and autoimmune disorders of the central nervous system, brain and spinal cord nervous system result from a targeted immune attack on neurons or glial cells in the central (e.g. encephal... --RELATED_TO--> [?] Opsoclonus-myoclonus Def: Opsoclonus-myoclonus (OM) is an autoimmune disorder of eye movements characterised by opsoclonus (involuntary unpredictable rapid eye movements [saccades] without inter-saccadic intervals), myoclonus ... --CHILD--> [?] Paraneoplastic opsoclonus myoclonus Def: Paraneoplastic opsoclonus myoclonus (OM) results from a targeted attack on the brainstem as a consequence of a potentially effective tumour immune response initiated by onco-neural antigens derived fr...
[ "[4A00.0Y] Other specified functional neutrophil defects\n --PARENT--> [4A00.0] Functional neutrophil defects\n --CHILD--> [4A00.0Y] Other specified functional neutrophil defects", "[4A00.0Y] Other specified functional neutrophil defects\n --PARENT--> [4A00.0] Functional neutrophil defects\n --CHILD--> [4A00.00] Neutrophil immunodeficiency syndrome\n Def: Neutrophil immunodeficiency syndrome is a primary immunodeficiency characterised by neutrophilia with severe neutrophil dysfunction, leukocytosis, a predisposition to bacterial infections and poor wou...", "[8A40.Y] Other specified multiple sclerosis\n --PARENT--> [8A40] Multiple sclerosis\n Def: Multiple Sclerosis (MS) is a chronic, inflammatory demyelinating disease of the central nervous system. Three categories of multiple sclerosis have been outlined: Relapsing/remitting, secondary progre...\n --CHILD--> [8A40.0] Relapsing-remitting multiple sclerosis\n Def: Clearly defined disease relapses with full recovery or with sequelae and residual deficit upon recovery. The periods between disease relapses are characterised by a lack of disease progression....", "[8A40.Y] Other specified multiple sclerosis\n --PARENT--> [8A40] Multiple sclerosis\n Def: Multiple Sclerosis (MS) is a chronic, inflammatory demyelinating disease of the central nervous system. Three categories of multiple sclerosis have been outlined: Relapsing/remitting, secondary progre...\n --CHILD--> [8A40.2] Secondary progressive multiple sclerosis", "[8E4A.0] Paraneoplastic or autoimmune disorders of the central nervous system, brain or spinal cord\n Def: Paraneoplastic and autoimmune disorders of the central nervous system, brain and spinal cord nervous system result from a targeted immune attack on neurons or glial cells in the central (e.g. encephal...\n --PARENT--> [8E4A] Paraneoplastic or autoimmune disorders of the nervous system\n Def: Paraneoplastic and autoimmune disorders of the nervous system result from a targeted immune attack on neurons or glial cells in the central (e.g. encephalopathy, ataxia, myelitis) or peripheral nervou...\n --PARENT--> [?] Certain disorders of the nervous system", "[8E4A.0] Paraneoplastic or autoimmune disorders of the central nervous system, brain or spinal cord\n Def: Paraneoplastic and autoimmune disorders of the central nervous system, brain and spinal cord nervous system result from a targeted immune attack on neurons or glial cells in the central (e.g. encephal...\n --RELATED_TO--> [?] Opsoclonus-myoclonus\n Def: Opsoclonus-myoclonus (OM) is an autoimmune disorder of eye movements characterised by opsoclonus (involuntary unpredictable rapid eye movements [saccades] without inter-saccadic intervals), myoclonus ...\n --CHILD--> [?] Paraneoplastic opsoclonus myoclonus\n Def: Paraneoplastic opsoclonus myoclonus (OM) results from a targeted attack on the brainstem as a consequence of a potentially effective tumour immune response initiated by onco-neural antigens derived fr..." ]
4A00.0Y
Other specified functional neutrophil defects
[ { "from_icd11": "8E4A.0", "icd10_code": "G3183", "icd10_title": "Dementia with Lewy bodies" }, { "from_icd11": "8E4A.0", "icd10_code": "G2581", "icd10_title": "Restless legs syndrome" }, { "from_icd11": "8E4A.0", "icd10_code": "G3184", "icd10_title": "Mild cognitive impairment, so stated" }, { "from_icd11": "8E4A.0", "icd10_code": "G9349", "icd10_title": "Other encephalopathy" }, { "from_icd11": "8E4A.0", "icd10_code": "G0481", "icd10_title": "Other encephalitis and encephalomyelitis" }, { "from_icd11": "8E4A.0", "icd10_code": "G9589", "icd10_title": "Other specified diseases of spinal cord" }, { "from_icd11": "8E4A.0", "icd10_code": "G2589", "icd10_title": "Other specified extrapyramidal and movement disorders" }, { "from_icd11": "8E4A.0", "icd10_code": "G3189", "icd10_title": "Other specified degenerative diseases of nervous system" }, { "from_icd11": "8E4A.0", "icd10_code": "G2582", "icd10_title": "Stiff-man syndrome" }, { "from_icd11": "8E4A.0", "icd10_code": "G0489", "icd10_title": "Other myelitis" }, { "from_icd11": "8E4A.0", "icd10_code": "G9581", "icd10_title": "Conus medullaris syndrome" }, { "from_icd11": "8E4A.0", "icd10_code": "G3185", "icd10_title": "Corticobasal degeneration" }, { "from_icd11": "8E4A.0", "icd10_code": "G3181", "icd10_title": "Alpers disease" }, { "from_icd11": "8E4A.0", "icd10_code": "G3182", "icd10_title": "Leigh's disease" }, { "from_icd11": "8E4A.0", "icd10_code": "G992", "icd10_title": "Myelopathy in diseases classified elsewhere" } ]
G3183
Dementia with Lewy bodies
Screening tests after birth suggested deafness. Hearing tests between the ages of 2 to 4 months were inconclusive. At 4 months, severe deafness was diagnosed using the Auditory Brainstem Response (ABR) test, with 70 dB (left) and 80–90 dB (right) auditory deficits. At age 3 and a half months, CT imaging revealed shadowing of the entire pneumatic structures of both pyramids, suggesting inner ear inflammation. His middle ear canals were drained, anti-inflammatory treatment was applied and bilateral hearing aids were used from 6 months. Brainstem auditory evoked potentials (BAEP) at 5 months and at 16 months were positive. Hearing tests at 3 years 4 months showed sensorineural hearing loss of medium degree with a reaction to sound at 35 dB and 40–45 dB with and without hearing aids, respectively. This reflects an appreciable regression of deafness, out of character for B-WS or isolated ACTG1 -related deafness, which are both normally progressive. We conclude that early infection of the ear canals and subsequent healing were responsible for the regressive nature of deafness in our patient, since hearing improved after drainage and anti-inflammatory treatment. We note that congenital malformations of the skull (microcephaly, brachycephaly) may contribute to an anomalous inner ear structure causing secretion and fluid accumulation, and a predisposition to ear canal infections exacerbating hearing loss.
4.191406
0.82959
sec[1]/sec[1]/p[0]
en
0.999997
PMC8776155
https://doi.org/10.3390/ijms23020692
[ "hearing", "deafness", "auditory", "brainstem", "both", "inner", "canals", "anti", "inflammatory", "aids" ]
[ { "code": "AB52", "title": "Deafness not otherwise specified" }, { "code": "QA00.7", "title": "Examination of ears and hearing" }, { "code": "MC4Y", "title": "Other specified symptoms or signs involving the ear or mastoid process" }, { "code": "AB54", "title": "Presbycusis" }, { "code": "AB5Z", "title": "Disorders with hearing impairment, unspecified" }, { "code": "AB51.Z", "title": "Acquired hearing impairment, unspecified" }, { "code": "MB4B.Y", "title": "Other specified symbolic dysfunctions" }, { "code": "AB56", "title": "Hereditary hearing loss" }, { "code": "AB51.0", "title": "Acquired conductive hearing loss" }, { "code": "6B60.1", "title": "Dissociative neurological symptom disorder, with auditory disturbance" } ]
=== ICD-11 CODES FOUND === [AB52] Deafness not otherwise specified Also known as: Deafness not otherwise specified | deaf | hearing loss NOS | hearing impairment | hearing loss [QA00.7] Examination of ears and hearing Also known as: Examination of ears and hearing | examination of ear | hearing examination | hearing test [MC4Y] Other specified symptoms or signs involving the ear or mastoid process Also known as: Other specified symptoms or signs involving the ear or mastoid process | Hearing complaint | Fear of ear disease [AB54] Presbycusis Definition: The term presbycusis refers to sensorineural hearing impairment in elderly individuals. Characteristically, presbycusis involves bilateral high-frequency hearing loss associated with difficulty in speech discrimination and central auditory processing of information. Also known as: Presbycusis | Presbyacusia | age-related hearing loss | senile deafness | hard of hearing Includes: Presbyacusia [AB5Z] Disorders with hearing impairment, unspecified Also known as: Disorders with hearing impairment, unspecified | disorders with hearing loss [AB51.Z] Acquired hearing impairment, unspecified Also known as: Acquired hearing impairment, unspecified | Acquired hearing impairment | post lingual hearing loss | acquired deafness [MB4B.Y] Other specified symbolic dysfunctions Also known as: Other specified symbolic dysfunctions | Amimia | Auditory amnesia | Amusia | Asymbolia [AB56] Hereditary hearing loss Also known as: Hereditary hearing loss | genetic hearing loss | hereditary deafness Excludes: Congenital hearing impairment | Acquired hearing impairment [AB51.0] Acquired conductive hearing loss Definition: Conductive hearing loss occurs when there is a problem conducting sound waves anywhere along the route through the outer ear, tympanic membrane (eardrum), or middle ear (ossicles), bilateral. Also known as: Acquired conductive hearing loss | conduction deafness [6B60.1] Dissociative neurological symptom disorder, with auditory disturbance Definition: Dissociative neurological symptom disorder, with auditory disturbance is characterised by auditory symptoms such as loss of hearing or auditory hallucinations that are not consistent with a recognised disease of the nervous system, other mental, behavioural or neurodevelopmental disorder, or other medical condition and do not occur exclusively during another dissociative disorder. Also known as: Dissociative neurological symptom disorder, with auditory disturbance | Functional neurological symptom disorder, with auditory symptoms | Functional neurological symptom disorder, with auditory disturbance | Functional auditory disorder === GRAPH WALKS === --- Walk 1 --- [AB52] Deafness not otherwise specified --PARENT--> [?] Disorders with hearing impairment --CHILD--> [AB52] Deafness not otherwise specified --- Walk 2 --- [AB52] Deafness not otherwise specified --PARENT--> [?] Disorders with hearing impairment --CHILD--> [AB50] Congenital hearing impairment Def: Both dominant and recessive genes exist which can cause mild to profound impairment. If a family has a dominant gene for deafness it will persist across generations because it will manifest itself in ... --- Walk 3 --- [QA00.7] Examination of ears and hearing --PARENT--> [QA00] General examination or investigation of persons without complaint or reported diagnosis --CHILD--> [QA00.2] Routine newborn health examination Def: Health examination for infant under 29 days of age... --- Walk 4 --- [QA00.7] Examination of ears and hearing --PARENT--> [QA00] General examination or investigation of persons without complaint or reported diagnosis --EXCLUDES--> [?] Special screening examination for neoplasms --- Walk 5 --- [MC4Y] Other specified symptoms or signs involving the ear or mastoid process --PARENT--> [?] Symptoms or signs involving the ear or mastoid process --PARENT--> [?] Symptoms, signs or clinical findings of ear or mastoid process --- Walk 6 --- [MC4Y] Other specified symptoms or signs involving the ear or mastoid process --PARENT--> [?] Symptoms or signs involving the ear or mastoid process --RELATED_TO--> [?] Otalgia or effusion of ear
[ "[AB52] Deafness not otherwise specified\n --PARENT--> [?] Disorders with hearing impairment\n --CHILD--> [AB52] Deafness not otherwise specified", "[AB52] Deafness not otherwise specified\n --PARENT--> [?] Disorders with hearing impairment\n --CHILD--> [AB50] Congenital hearing impairment\n Def: Both dominant and recessive genes exist which can cause mild to profound impairment. If a family has a dominant gene for deafness it will persist across generations because it will manifest itself in ...", "[QA00.7] Examination of ears and hearing\n --PARENT--> [QA00] General examination or investigation of persons without complaint or reported diagnosis\n --CHILD--> [QA00.2] Routine newborn health examination\n Def: Health examination for infant under 29 days of age...", "[QA00.7] Examination of ears and hearing\n --PARENT--> [QA00] General examination or investigation of persons without complaint or reported diagnosis\n --EXCLUDES--> [?] Special screening examination for neoplasms", "[MC4Y] Other specified symptoms or signs involving the ear or mastoid process\n --PARENT--> [?] Symptoms or signs involving the ear or mastoid process\n --PARENT--> [?] Symptoms, signs or clinical findings of ear or mastoid process", "[MC4Y] Other specified symptoms or signs involving the ear or mastoid process\n --PARENT--> [?] Symptoms or signs involving the ear or mastoid process\n --RELATED_TO--> [?] Otalgia or effusion of ear" ]
AB52
Deafness not otherwise specified
[ { "from_icd11": "AB52", "icd10_code": "H9190", "icd10_title": "Unspecified hearing loss, unspecified ear" }, { "from_icd11": "AB52", "icd10_code": "H9193", "icd10_title": "Unspecified hearing loss, bilateral" }, { "from_icd11": "QA00.7", "icd10_code": "Z011", "icd10_title": "Encounter for examination of ears and hearing" }, { "from_icd11": "AB54", "icd10_code": "H9113", "icd10_title": "Presbycusis, bilateral" }, { "from_icd11": "AB54", "icd10_code": "H9110", "icd10_title": "Presbycusis, unspecified ear" }, { "from_icd11": "AB54", "icd10_code": "H911", "icd10_title": "Presbycusis" }, { "from_icd11": "AB5Z", "icd10_code": "H9192", "icd10_title": "Unspecified hearing loss, left ear" }, { "from_icd11": "AB5Z", "icd10_code": "H9191", "icd10_title": "Unspecified hearing loss, right ear" }, { "from_icd11": "AB5Z", "icd10_code": "H9011", "icd10_title": "Conductive hearing loss, unilateral, right ear, with unrestricted hearing on the contralateral side" }, { "from_icd11": "AB5Z", "icd10_code": "H918X3", "icd10_title": "Other specified hearing loss, bilateral" }, { "from_icd11": "AB5Z", "icd10_code": "H918X9", "icd10_title": "Other specified hearing loss, unspecified ear" }, { "from_icd11": "AB5Z", "icd10_code": "H918X2", "icd10_title": "Other specified hearing loss, left ear" }, { "from_icd11": "AB5Z", "icd10_code": "H918X1", "icd10_title": "Other specified hearing loss, right ear" }, { "from_icd11": "AB5Z", "icd10_code": "H9012", "icd10_title": "Conductive hearing loss, unilateral, left ear, with unrestricted hearing on the contralateral side" }, { "from_icd11": "AB5Z", "icd10_code": "H913", "icd10_title": "Deaf nonspeaking, not elsewhere classified" } ]
H9190
Unspecified hearing loss, unspecified ear
A 77-year-old immunocompetent man presented with a massive ulcerated bleeding lesion on the lower lip extending to the oral cavity mucosa . He was a heavily smoker with no history of recent travel abroad; he only reported a traumatic cut in the lesioned area. In the suspicion of malignancy, the lesion was biopsied; histology revealed an intense chronic flogistic reaction and dysplastic aspects, consistent with a traumatic lesion. Owing to the persistence of symptoms, the patient was re-biopsied; specimens showed a mixed inflammatory infiltrate with leishmanial amastigotes detected by H&E and Giemsa staining. CD1a immunohistochemistry showed numerous Leishmania amastigotes, and leishmanial DNA was also detected in the biopsy specimen by the two PCR assays amplifying a fragment of the small-subunit rRNA gene as well as of the kinetoplast DNA, respectively. Molecular typing indicated the presence of L. infantum . The patient underwent a multivalent therapy, including cryotherapy, intralesional meglumine antimoniate (one injection/week) and IM pentamidine isethionate injections (one per week, 3 mg/kg for six weeks), with only partial remission. Subsequent dermoscopy still showed pathological aspects and therapy was modified to oral miltefosine 150 mg/day for one month, allopurinol 300 mg/day for three months and fluconazole 200 mg/day for three weeks , with complete remission at a 3-month follow-up .
4.101563
0.975586
sec[1]/sec[2]/p[0]
en
0.999996
32325735
https://doi.org/10.3390/microorganisms8040588
[ "lesion", "oral", "traumatic", "biopsied", "aspects", "leishmanial", "amastigotes", "remission", "three", "immunocompetent" ]
[ { "code": "FA5Z", "title": "Arthropathies, unspecified" }, { "code": "FC0Z", "title": "Diseases of the musculoskeletal system or connective tissue, unspecified" }, { "code": "ME60.Z", "title": "Skin lesion of unspecified nature" }, { "code": "MD41", "title": "Clinical findings on diagnostic imaging of lung" }, { "code": "GC2Z&XA6KU8", "title": "Disease of kidney, not elsewhere classified" }, { "code": "MD11.8Z", "title": "Mouth breathing, unspecified" }, { "code": "DA01.00", "title": "Oral leukoplakia" }, { "code": "DA01.10", "title": "Oral aphthae or aphtha-like ulceration" }, { "code": "MD80.1", "title": "Symptom or complaint of the mouth, tongue or lip" }, { "code": "DA01.1Y", "title": "Other specified noninfectious erosive or ulcerative disorders of oral mucosa" } ]
=== ICD-11 CODES FOUND === [FA5Z] Arthropathies, unspecified Also known as: Arthropathies, unspecified | Disorders affecting predominantly peripheral joints | Disorders affecting predominantly peripheral limb joints | arthropathy NOS | arthropathic [FC0Z] Diseases of the musculoskeletal system or connective tissue, unspecified Also known as: Diseases of the musculoskeletal system or connective tissue, unspecified | bone disease NOS | bone disorder NOS | bone lesion NOS | musculoskeletal complications NOS [ME60.Z] Skin lesion of unspecified nature Also known as: Skin lesion of unspecified nature | Skin lesion of uncertain or unspecified nature | Skin lesion without established diagnosis | Pigmented skin lesion of unspecified nature | Ulcer of skin of unspecified nature [MD41] Clinical findings on diagnostic imaging of lung Definition: Clinical findings on diagnostic imaging of lung is findings on diagnostic imaging of the lung which don't appear in normal status of the body. Diagnostic imaging refers to technologies that doctors use to look inside body for clues about a medical condition. X-rays, CT scans, nuclear medicine scans, MRI scans and ultrasound are all types of diagnostic imaging. Also known as: Clinical findings on diagnostic imaging of lung | abnormal diagnostic imaging of lung | Hyperinflation of lung | Lung mass | Pulmonary lobe mass [MD11.8Z] Mouth breathing, unspecified Also known as: Mouth breathing, unspecified | Mouth breathing | breathing orally | mouth respiration [DA01.00] Oral leukoplakia Definition: Leukoplakia is a condition where areas of keratosis appear as adherent white patches on the mucous membranes of the oral cavity. Leukoplakia may affect other gastrointestinal tract mucosal sites, or mucosal surfaces of the urinary tract and genitals. Also known as: Oral leukoplakia | Leukoplakia of gingiva | leukoplakia of oral epithelium | leucoplakia of oral mucosa | leukokeratosis of oral mucosa Includes: Leukoplakia of gingiva Excludes: Hairy leukoplakia [DA01.10] Oral aphthae or aphtha-like ulceration Definition: This is a frequent small, shallow, painful ulceration in the oral mucosa. Recurrent oral ulceration that clinically resembles recurrent aphthous stomatitis but presents atypically, including commencement after adolescence, with fever, with a strong family history, or failing to resolve with age. Also known as: Oral aphthae or aphtha-like ulceration | Recurrent aphthous stomatitis | Recurrent oral aphthae | Major recurrent aphthous stomatitis | major aphthous stomatitis [MD80.1] Symptom or complaint of the mouth, tongue or lip Also known as: Symptom or complaint of the mouth, tongue or lip | Mouth swelling | mouth oedema | swollen mouth | Lip swelling [DA01.1Y] Other specified noninfectious erosive or ulcerative disorders of oral mucosa Also known as: Other specified noninfectious erosive or ulcerative disorders of oral mucosa | Oral ulceration due to immunobullous disease | Oral mucosal involvement by immunobullous disorder classified elsewhere | Oral ulceration due to physical injury | Mechanical oral ulceration === GRAPH WALKS === --- Walk 1 --- [FA5Z] Arthropathies, unspecified --PARENT--> [?] Arthropathies --CHILD--> [?] Infection related arthropathies Def: A disease of the joints, caused by an infection with a bacterial, viral, fungal, or parasitic source. Distinction is made between the following types of etiological relationship. a) direct infection ... --- Walk 2 --- [FA5Z] Arthropathies, unspecified --PARENT--> [?] Arthropathies --CHILD--> [?] Inflammatory arthropathies --- Walk 3 --- [FC0Z] Diseases of the musculoskeletal system or connective tissue, unspecified --PARENT--> [15] Diseases of the musculoskeletal system or connective tissue Def: This chapter contains diseases of musculoskeletal system and diseases of connective tissue.... --EXCLUDES--> [?] Endocrine, nutritional or metabolic diseases Def: This chapter includes endocrine diseases, nutritional diseases as well as metabolic diseases.... --- Walk 4 --- [FC0Z] Diseases of the musculoskeletal system or connective tissue, unspecified --PARENT--> [15] Diseases of the musculoskeletal system or connective tissue Def: This chapter contains diseases of musculoskeletal system and diseases of connective tissue.... --RELATED_TO--> [?] Symptoms, signs or clinical findings of the musculoskeletal system --- Walk 5 --- [ME60.Z] Skin lesion of unspecified nature --PARENT--> [ME60] Skin lesion of uncertain or unspecified nature Def: To be used where there is either significant uncertainty or alternatively no information as to the nature of a circumscribed skin lesion. This is of particular importance with regard to whether or not... --CHILD--> [ME60.0] Skin lesion of uncertain nature Def: This denotes the presence of a skin lesion but uncertainty as to its nature. No inference as to whether the lesion might be of serious significance (e.g. suspected skin cancer) is made.... --- Walk 6 --- [ME60.Z] Skin lesion of unspecified nature --PARENT--> [ME60] Skin lesion of uncertain or unspecified nature Def: To be used where there is either significant uncertainty or alternatively no information as to the nature of a circumscribed skin lesion. This is of particular importance with regard to whether or not... --CHILD--> [ME60.1] Pigmented skin lesion of uncertain nature Def: This denotes the presence of a pigmented skin lesion but uncertainty as to its nature. No inference as to whether the lesion might be of serious significance (e.g. suspected skin cancer) is made....
[ "[FA5Z] Arthropathies, unspecified\n --PARENT--> [?] Arthropathies\n --CHILD--> [?] Infection related arthropathies\n Def: A disease of the joints, caused by an infection with a bacterial, viral, fungal, or parasitic source.\n\nDistinction is made between the following types of etiological relationship.\na) direct infection ...", "[FA5Z] Arthropathies, unspecified\n --PARENT--> [?] Arthropathies\n --CHILD--> [?] Inflammatory arthropathies", "[FC0Z] Diseases of the musculoskeletal system or connective tissue, unspecified\n --PARENT--> [15] Diseases of the musculoskeletal system or connective tissue\n Def: This chapter contains diseases of musculoskeletal system and diseases of connective tissue....\n --EXCLUDES--> [?] Endocrine, nutritional or metabolic diseases\n Def: This chapter includes endocrine diseases, nutritional diseases as well as metabolic diseases....", "[FC0Z] Diseases of the musculoskeletal system or connective tissue, unspecified\n --PARENT--> [15] Diseases of the musculoskeletal system or connective tissue\n Def: This chapter contains diseases of musculoskeletal system and diseases of connective tissue....\n --RELATED_TO--> [?] Symptoms, signs or clinical findings of the musculoskeletal system", "[ME60.Z] Skin lesion of unspecified nature\n --PARENT--> [ME60] Skin lesion of uncertain or unspecified nature\n Def: To be used where there is either significant uncertainty or alternatively no information as to the nature of a circumscribed skin lesion. This is of particular importance with regard to whether or not...\n --CHILD--> [ME60.0] Skin lesion of uncertain nature\n Def: This denotes the presence of a skin lesion but uncertainty as to its nature. No inference as to whether the lesion might be of serious significance (e.g. suspected skin cancer) is made....", "[ME60.Z] Skin lesion of unspecified nature\n --PARENT--> [ME60] Skin lesion of uncertain or unspecified nature\n Def: To be used where there is either significant uncertainty or alternatively no information as to the nature of a circumscribed skin lesion. This is of particular importance with regard to whether or not...\n --CHILD--> [ME60.1] Pigmented skin lesion of uncertain nature\n Def: This denotes the presence of a pigmented skin lesion but uncertainty as to its nature. No inference as to whether the lesion might be of serious significance (e.g. suspected skin cancer) is made...." ]
FA5Z
Arthropathies, unspecified
[ { "from_icd11": "FA5Z", "icd10_code": "M00-M25", "icd10_title": "" }, { "from_icd11": "FC0Z", "icd10_code": "XIII", "icd10_title": "" }, { "from_icd11": "ME60.Z", "icd10_code": "L989", "icd10_title": "Disorder of the skin and subcutaneous tissue, unspecified" }, { "from_icd11": "MD41", "icd10_code": "R911", "icd10_title": "Solitary pulmonary nodule" }, { "from_icd11": "MD41", "icd10_code": "R91", "icd10_title": "Abnormal findings on diagnostic imaging of lung" }, { "from_icd11": "MD11.8Z", "icd10_code": "R065", "icd10_title": "Mouth breathing" }, { "from_icd11": "DA01.00", "icd10_code": "K1329", "icd10_title": "Other disturbances of oral epithelium, including tongue" }, { "from_icd11": "DA01.00", "icd10_code": "K1321", "icd10_title": "Leukoplakia of oral mucosa, including tongue" }, { "from_icd11": "DA01.00", "icd10_code": "K132", "icd10_title": "Leukoplakia and other disturbances of oral epithelium, including tongue" }, { "from_icd11": "DA01.10", "icd10_code": "K120", "icd10_title": "Recurrent oral aphthae" } ]
M00-M25
Up to one-third of patients with CCRC will have metastatic disease at the time of diagnosis . Many individuals will have metastatic disease in multiple organ sites, with a mean of four organs involved; however, it is not common for RCC to metastasize to the colon or rectum . Our patient had pulmonary, hepatic, and colorectal metastases at the time of diagnosis. The colorectal involvement manifested as obstruction and bleeding. The most common site of gastrointestinal RCC metastasis is the stomach, although the prevalence is so low that the probability of a second primary tumor is more likely than the occurrence of RCC metastasis to the stomach . It is estimated that small intestine involvement is only present in 3-4% of patients with RCC . Of the few cases involving the gastrointestinal tract, there have only been 10 cases of metastatic RCC presenting with lower gastrointestinal bleeding, and none of those cases could confirm the presence of metastasis as a result of direct invasion . The exact incidence of colonic involvement in the general population is unknown . Approximately 61 cases of rectal metastasis of CCRC in ADPKD patients have been recorded since 1954; however, all patients were previously diagnosed with primary tumors of the kidneys . Our case is very rare because our patient had benign kidney disease before being diagnosed with metastatic CCRC to his colon, rectum, liver, and lungs.
4.105469
0.69873
sec[2]/p[1]
en
0.999996
PMC8963926
https://doi.org/10.7759/cureus.22659
[ "patients", "metastatic", "metastasis", "cases", "ccrc", "involvement", "gastrointestinal", "time", "however", "common" ]
[ { "code": "PL14.C", "title": "Patient received diagnostic test or treatment intended for another patient" }, { "code": "QB14", "title": "Unavailability or inaccessibility of health care facilities" }, { "code": "PL14.2", "title": "Problem associated with physical transfer of patient" }, { "code": "QB12.0", "title": "Organ transplant candidate" }, { "code": "QA15.1", "title": "Counselling related to sexual behaviour and orientation or sexual relationships of the person" }, { "code": "2D4Z", "title": "Unspecified malignant neoplasms of unspecified sites" }, { "code": "5C64.5", "title": "Disorders of calcium metabolism" }, { "code": "2E2Z", "title": "Malignant neoplasm metastasis, unspecified" }, { "code": "2E03", "title": "Malignant neoplasm metastasis in bone or bone marrow" }, { "code": "2D70", "title": "Malignant neoplasm metastasis in lung" } ]
=== ICD-11 CODES FOUND === [PL14.C] Patient received diagnostic test or treatment intended for another patient Also known as: Patient received diagnostic test or treatment intended for another patient | wrong patient | incorrect patient Excludes: Procedure undertaken at wrong site or wrong side, as mode of injury or harm [QB14] Unavailability or inaccessibility of health care facilities Also known as: Unavailability or inaccessibility of health care facilities | unavailability of medical facilities | Unavailability of outpatient clinic | Unavailability or inaccessibility of residential aged care service Excludes: bed unavailable [PL14.2] Problem associated with physical transfer of patient Also known as: Problem associated with physical transfer of patient [QB12.0] Organ transplant candidate Also known as: Organ transplant candidate | patient waiting for organ availability | health services provided because of need for organ transplant | organ transplant candidate awaiting organ availability | person on organ transplant waiting list [QA15.1] Counselling related to sexual behaviour and orientation or sexual relationships of the person Also known as: Counselling related to sexual behaviour and orientation or sexual relationships of the person | advice on sexual behaviour or orientation | counselling on sexual behaviour or orientation | promiscuity counselling | patient concerned regarding sexual orientation [2D4Z] Unspecified malignant neoplasms of unspecified sites Also known as: Unspecified malignant neoplasms of unspecified sites | malignancy of unspecified site | malignancy unspecified primary site | malignant growth of unspecified site | malignant mass of unspecified site [5C64.5] Disorders of calcium metabolism Definition: This refers to disorders in the mechanism by which the body maintains adequate calcium levels. Derangements of this mechanism lead to hypercalcaemia or hypocalcaemia, both of which can have important consequences for health. Also known as: Disorders of calcium metabolism | Calcinosis | general calcification | heterotopic calcification | metastatic calcification Excludes: Hyperparathyroidism | Chondrocalcinosis [2E2Z] Malignant neoplasm metastasis, unspecified Also known as: Malignant neoplasm metastasis, unspecified | secondary malignant neoplasm | metastasis | metastases | disseminated metastases [2E03] Malignant neoplasm metastasis in bone or bone marrow Definition: The spread of a malignant neoplasm from a primary site to the skeletal system. The majority of metastatic neoplasms to the bone are carcinomas. Also known as: Malignant neoplasm metastasis in bone or bone marrow | bone metastasis | bony metastasis | osseous metastasis | secondary cancer of bone [2D70] Malignant neoplasm metastasis in lung Also known as: Malignant neoplasm metastasis in lung | metastasis in lung | pulmonary metastasis | secondary cancer in lung | secondary malignant tumour in lung Excludes: Malignant neoplasms of bronchus or lung === GRAPH WALKS === --- Walk 1 --- [PL14.C] Patient received diagnostic test or treatment intended for another patient --EXCLUDES--> [?] Procedure undertaken at wrong site or wrong side, as mode of injury or harm --CHILD--> [?] Performance of inappropriate operation --- Walk 2 --- [PL14.C] Patient received diagnostic test or treatment intended for another patient --EXCLUDES--> [?] Procedure undertaken at wrong site or wrong side, as mode of injury or harm --PARENT--> [?] Mode of injury or harm associated with a surgical or other medical procedure --- Walk 3 --- [QB14] Unavailability or inaccessibility of health care facilities --PARENT--> [?] Factors related to medical facilities or other health care --CHILD--> [QB12] Waiting period for investigation or treatment other than awaiting admission to adequate facility elsewhere --- Walk 4 --- [QB14] Unavailability or inaccessibility of health care facilities --EXCLUDES--> [?] Person awaiting admission to adequate facility elsewhere --CHILD--> [?] Person awaiting admission to residential aged care service --- Walk 5 --- [PL14.2] Problem associated with physical transfer of patient --PARENT--> [PL14] Mode of injury or harm associated with other health care related causes --EXCLUDES--> [?] Mode of injury or harm associated with a surgical or other medical device, implant or graft --- Walk 6 --- [PL14.2] Problem associated with physical transfer of patient --PARENT--> [PL14] Mode of injury or harm associated with other health care related causes --EXCLUDES--> [?] Mode of injury or harm associated with a surgical or other medical device, implant or graft
[ "[PL14.C] Patient received diagnostic test or treatment intended for another patient\n --EXCLUDES--> [?] Procedure undertaken at wrong site or wrong side, as mode of injury or harm\n --CHILD--> [?] Performance of inappropriate operation", "[PL14.C] Patient received diagnostic test or treatment intended for another patient\n --EXCLUDES--> [?] Procedure undertaken at wrong site or wrong side, as mode of injury or harm\n --PARENT--> [?] Mode of injury or harm associated with a surgical or other medical procedure", "[QB14] Unavailability or inaccessibility of health care facilities\n --PARENT--> [?] Factors related to medical facilities or other health care\n --CHILD--> [QB12] Waiting period for investigation or treatment other than awaiting admission to adequate facility elsewhere", "[QB14] Unavailability or inaccessibility of health care facilities\n --EXCLUDES--> [?] Person awaiting admission to adequate facility elsewhere\n --CHILD--> [?] Person awaiting admission to residential aged care service", "[PL14.2] Problem associated with physical transfer of patient\n --PARENT--> [PL14] Mode of injury or harm associated with other health care related causes\n --EXCLUDES--> [?] Mode of injury or harm associated with a surgical or other medical device, implant or graft", "[PL14.2] Problem associated with physical transfer of patient\n --PARENT--> [PL14] Mode of injury or harm associated with other health care related causes\n --EXCLUDES--> [?] Mode of injury or harm associated with a surgical or other medical device, implant or graft" ]
PL14.C
Patient received diagnostic test or treatment intended for another patient
[ { "from_icd11": "QB14", "icd10_code": "Z753", "icd10_title": "Unavailability and inaccessibility of health-care facilities" }, { "from_icd11": "QA15.1", "icd10_code": "F66", "icd10_title": "Other sexual disorders" }, { "from_icd11": "QA15.1", "icd10_code": "F660", "icd10_title": "" }, { "from_icd11": "QA15.1", "icd10_code": "F661", "icd10_title": "" }, { "from_icd11": "QA15.1", "icd10_code": "F662", "icd10_title": "" }, { "from_icd11": "QA15.1", "icd10_code": "F668", "icd10_title": "" }, { "from_icd11": "QA15.1", "icd10_code": "F669", "icd10_title": "" }, { "from_icd11": "QA15.1", "icd10_code": "Z701", "icd10_title": "Counseling related to patient's sexual behavior and orientation" }, { "from_icd11": "2D4Z", "icd10_code": "C802", "icd10_title": "Malignant neoplasm associated with transplanted organ" }, { "from_icd11": "2D4Z", "icd10_code": "C7650", "icd10_title": "Malignant neoplasm of unspecified lower limb" }, { "from_icd11": "2D4Z", "icd10_code": "C7642", "icd10_title": "Malignant neoplasm of left upper limb" }, { "from_icd11": "2D4Z", "icd10_code": "C7640", "icd10_title": "Malignant neoplasm of unspecified upper limb" }, { "from_icd11": "2D4Z", "icd10_code": "C7652", "icd10_title": "Malignant neoplasm of left lower limb" }, { "from_icd11": "2D4Z", "icd10_code": "C7651", "icd10_title": "Malignant neoplasm of right lower limb" }, { "from_icd11": "2D4Z", "icd10_code": "C7641", "icd10_title": "Malignant neoplasm of right upper limb" } ]
Z753
Unavailability and inaccessibility of health-care facilities
On day 1 after TAE, the cat's body temperature increased to 39.5°C, and the serum alanine aminotransferase (ALT) level increased to 303 U/L (reference range, 22–84 U/L). Therefore, lactated Ringer's solution was infused intravenously (3.0 mL/kg/h). On day 3 after TAE, the body temperature decreased to 38.6°C, and administration of lactated Ringer's solution was stopped. The cat was discharged 5 days after TAE. The ALT level, which was at its highest on postoperative day 1, gradually decreased from day 2 and eventually normalized to 66 U/L on day 11 after TAE. Moreover, there was no significant increase in alkaline phosphatase levels after embolization. Abdominal ultrasonography showed gradual disappearance of fluid in the abdominal cavity, and there was no fluid in the peritoneal cavity at discharge. At the time of discharge, the general condition of the cat was stable, both vigor and appetite were good„ and PCV had increased to 25%. After discharge, the cat's condition remained stable, and no further intra-abdominal bleeding occurred. The remaining mass was surgically removed 66 days after TAE. CT performed before resection revealed a reduction in the mass's longest diameter from 32 × 45 × 52 mm to 22 × 43 × 32 mm (a partial response) . Histopathological examination of the resected mass revealed a cholangiocellular adenoma. The cat was doing well at the last follow-up visit on day 549 after TAE.
3.787109
0.977539
sec[2]/sec[2]/p[0]
en
0.999995
34409090
https://doi.org/10.3389/fvets.2021.707120
[ "abdominal", "body", "temperature", "lactated", "ringer", "solution", "fluid", "cavity", "serum", "alanine" ]
[ { "code": "MD81.3", "title": "Acute abdomen" }, { "code": "JA01.0", "title": "Abdominal pregnancy" }, { "code": "ME04.Z", "title": "Ascites, unspecified" }, { "code": "NB51.0&XA3KX0", "title": "Laceration without foreign body of abdominal wall" }, { "code": "NB9Y", "title": "Other specified injuries to the abdomen, lower back, lumbar spine or pelvis" }, { "code": "ND51.Y", "title": "Other specified injuries of spine or trunk, level unspecified" }, { "code": "MG20.Z", "title": "Cachexia, unspecified" }, { "code": "ND56.Z", "title": "Unspecified injury to unspecified part of trunk, limb or body region" }, { "code": "8A22", "title": "Lewy body disease" }, { "code": "ME86.Z", "title": "Problem of unspecified body part" } ]
=== ICD-11 CODES FOUND === [MD81.3] Acute abdomen Definition: A clinical syndrome with acute abdominal pain that is severe, and rapid onset. Acute abdomen may be caused by a variety of disorders, injuries, or diseases Also known as: Acute abdomen | acute abdominal pain syndrome | surgical abdomen | abdominal acute syndrome | severe abdomen pain [JA01.0] Abdominal pregnancy Definition: A condition characterised by implantation of the embryo within the peritoneal cavity during pregnancy. Also known as: Abdominal pregnancy | abdomen pregnancy | intraperitoneal pregnancy Excludes: Maternal care for viable fetus in abdominal pregnancy | Delivery of viable fetus in abdominal pregnancy [ME04.Z] Ascites, unspecified Also known as: Ascites, unspecified | Ascites | abdominal dropsy | hydrops abdominis | ascites NOS [NB9Y] Other specified injuries to the abdomen, lower back, lumbar spine or pelvis Also known as: Other specified injuries to the abdomen, lower back, lumbar spine or pelvis | Abdominal wall trauma | Injury of pelvic floor | pelvic floor blunt injury | pelvic floor blunt trauma [ND51.Y] Other specified injuries of spine or trunk, level unspecified Also known as: Other specified injuries of spine or trunk, level unspecified | Superficial injury of trunk, level unspecified | multiple superficial injuries of trunk | Abrasion of trunk, level unspecified | Contusion of trunk, level unspecified [MG20.Z] Cachexia, unspecified Also known as: Cachexia, unspecified | Cachexia | cachectic | general body deterioration | inanition [ND56.Z] Unspecified injury to unspecified part of trunk, limb or body region Also known as: Unspecified injury to unspecified part of trunk, limb or body region | Injury of unspecified body region | injury NOS | trauma NOS | traumatic injury NOS [8A22] Lewy body disease Definition: Lewy body disease is a neurodegenerative disorder and the second most common form of dementia in the elderly after Alzheimer disease. Lewy bodies are histologically defined as intracytoplasmic eosinophilic neuronal inclusions in the cortex or brainstem. Also known as: Lewy body disease | Lewy body | DLBD - [diffuse Lewy body disease] | diffuse Lewy body disease | CLBD - [cortical Lewy body disease] [ME86.Z] Problem of unspecified body part Also known as: Problem of unspecified body part | Symptom or complaint of a body part === GRAPH WALKS === --- Walk 1 --- [MD81.3] Acute abdomen Def: A clinical syndrome with acute abdominal pain that is severe, and rapid onset. Acute abdomen may be caused by a variety of disorders, injuries, or diseases... --PARENT--> [MD81] Abdominal or pelvic pain Def: Pain, an unpleasant distress sensation occurring in varying degrees of severity, received by nerve ending in the abdominal and pelvic region.... --EXCLUDES--> [?] Spinal pain Def: This is a condition characterised by pain felt in the back that usually originates from the muscles, nerves, bones, joints or other structures in the spine.... --- Walk 2 --- [MD81.3] Acute abdomen Def: A clinical syndrome with acute abdominal pain that is severe, and rapid onset. Acute abdomen may be caused by a variety of disorders, injuries, or diseases... --PARENT--> [MD81] Abdominal or pelvic pain Def: Pain, an unpleasant distress sensation occurring in varying degrees of severity, received by nerve ending in the abdominal and pelvic region.... --EXCLUDES--> [?] Spinal pain Def: This is a condition characterised by pain felt in the back that usually originates from the muscles, nerves, bones, joints or other structures in the spine.... --- Walk 3 --- [JA01.0] Abdominal pregnancy Def: A condition characterised by implantation of the embryo within the peritoneal cavity during pregnancy.... --EXCLUDES--> [?] Maternal care for viable fetus in abdominal pregnancy --PARENT--> [?] Maternal care for other fetal problems Def: A condition characterised by the provision of health interventions to the mother due to any other issue that is either suspected or known to be present in the fetus.... --- Walk 4 --- [JA01.0] Abdominal pregnancy Def: A condition characterised by implantation of the embryo within the peritoneal cavity during pregnancy.... --EXCLUDES--> [?] Delivery of viable fetus in abdominal pregnancy Def: A condition caused by the development of a viable fetus to the culmination of the pregnancy period. This condition is characterised by parturition of a viable neonate from the abdominal cavity, at the... --PARENT--> [?] Other assisted single delivery --- Walk 5 --- [ME04.Z] Ascites, unspecified --PARENT--> [ME04] Ascites Def: Accumulation or retention of free fluid in the abdominal peritoneal cavity between the tissues lining the abdomen and abdominal organs. The fluid may be serous, haemorrhagic, or the result of inflamma... --CHILD--> [ME04.Y] Other specified ascites --- Walk 6 --- [ME04.Z] Ascites, unspecified --PARENT--> [ME04] Ascites Def: Accumulation or retention of free fluid in the abdominal peritoneal cavity between the tissues lining the abdomen and abdominal organs. The fluid may be serous, haemorrhagic, or the result of inflamma... --CHILD--> [ME04.Z] Ascites, unspecified
[ "[MD81.3] Acute abdomen\n Def: A clinical syndrome with acute abdominal pain that is severe, and rapid onset. Acute abdomen may be caused by a variety of disorders, injuries, or diseases...\n --PARENT--> [MD81] Abdominal or pelvic pain\n Def: Pain, an unpleasant distress sensation occurring in varying degrees of severity, received by nerve ending in the abdominal and pelvic region....\n --EXCLUDES--> [?] Spinal pain\n Def: This is a condition characterised by pain felt in the back that usually originates from the muscles, nerves, bones, joints or other structures in the spine....", "[MD81.3] Acute abdomen\n Def: A clinical syndrome with acute abdominal pain that is severe, and rapid onset. Acute abdomen may be caused by a variety of disorders, injuries, or diseases...\n --PARENT--> [MD81] Abdominal or pelvic pain\n Def: Pain, an unpleasant distress sensation occurring in varying degrees of severity, received by nerve ending in the abdominal and pelvic region....\n --EXCLUDES--> [?] Spinal pain\n Def: This is a condition characterised by pain felt in the back that usually originates from the muscles, nerves, bones, joints or other structures in the spine....", "[JA01.0] Abdominal pregnancy\n Def: A condition characterised by implantation of the embryo within the peritoneal cavity during pregnancy....\n --EXCLUDES--> [?] Maternal care for viable fetus in abdominal pregnancy\n --PARENT--> [?] Maternal care for other fetal problems\n Def: A condition characterised by the provision of health interventions to the mother due to any other issue that is either suspected or known to be present in the fetus....", "[JA01.0] Abdominal pregnancy\n Def: A condition characterised by implantation of the embryo within the peritoneal cavity during pregnancy....\n --EXCLUDES--> [?] Delivery of viable fetus in abdominal pregnancy\n Def: A condition caused by the development of a viable fetus to the culmination of the pregnancy period. This condition is characterised by parturition of a viable neonate from the abdominal cavity, at the...\n --PARENT--> [?] Other assisted single delivery", "[ME04.Z] Ascites, unspecified\n --PARENT--> [ME04] Ascites\n Def: Accumulation or retention of free fluid in the abdominal peritoneal cavity between the tissues lining the abdomen and abdominal organs. The fluid may be serous, haemorrhagic, or the result of inflamma...\n --CHILD--> [ME04.Y] Other specified ascites", "[ME04.Z] Ascites, unspecified\n --PARENT--> [ME04] Ascites\n Def: Accumulation or retention of free fluid in the abdominal peritoneal cavity between the tissues lining the abdomen and abdominal organs. The fluid may be serous, haemorrhagic, or the result of inflamma...\n --CHILD--> [ME04.Z] Ascites, unspecified" ]
MD81.3
Acute abdomen
[ { "from_icd11": "MD81.3", "icd10_code": "R100", "icd10_title": "Acute abdomen" }, { "from_icd11": "JA01.0", "icd10_code": "O0000", "icd10_title": "Abdominal pregnancy without intrauterine pregnancy" }, { "from_icd11": "JA01.0", "icd10_code": "O000", "icd10_title": "Abdominal pregnancy" }, { "from_icd11": "ME04.Z", "icd10_code": "R180", "icd10_title": "Malignant ascites" }, { "from_icd11": "ME04.Z", "icd10_code": "R18", "icd10_title": "Ascites" }, { "from_icd11": "ND51.Y", "icd10_code": "S30860A", "icd10_title": "Insect bite (nonvenomous) of lower back and pelvis, initial encounter" }, { "from_icd11": "ND51.Y", "icd10_code": "S30861A", "icd10_title": "Insect bite (nonvenomous) of abdominal wall, initial encounter" }, { "from_icd11": "MG20.Z", "icd10_code": "R627", "icd10_title": "Adult failure to thrive" }, { "from_icd11": "MG20.Z", "icd10_code": "R64", "icd10_title": "Cachexia" }, { "from_icd11": "ND56.Z", "icd10_code": "T1491XA", "icd10_title": "Suicide attempt, initial encounter" }, { "from_icd11": "ND56.Z", "icd10_code": "T1490XS", "icd10_title": "Injury, unspecified, sequela" }, { "from_icd11": "ND56.Z", "icd10_code": "T1490", "icd10_title": "Injury, unspecified" }, { "from_icd11": "ND56.Z", "icd10_code": "T1491", "icd10_title": "Suicide attempt" }, { "from_icd11": "ND56.Z", "icd10_code": "T1490XA", "icd10_title": "Injury, unspecified, initial encounter" }, { "from_icd11": "ND56.Z", "icd10_code": "T148XXS", "icd10_title": "Other injury of unspecified body region, sequela" } ]
R100
Acute abdomen
Pulmonary veno-occlusive disease (PVOD) is a kind of rare and fatal pulmonary arterial hypertension (PAH), which is difficult to diagnose and treat. It was first described by Dr. Julius Hora of Munich University in 1934 that PVOD is characterized by widespread occlusion of the pulmonary venules by fibrous tissue. The reported incidence rate of PVOD is 0.1 to 0.2 cases per million every year. Patients usually present with nonspecific respiratory and/or cardiac symptoms, including shortness of breath, dyspnea on exertion, fatigue, chest pain, dizziness, cough, and hemoptysis. PVOD is a clinicopathological entity with the diagnosis based on clinical manifestations and tissue confirmation. A combined picture of PAH along with concurrent pulmonary edema findings on diagnostic imaging is usually the initial hint toward PVOD diagnosis. The gold standard for diagnosis is lung biopsy, which usually shows pulmonary venules intimal fibrosis with diffuse smooth muscle narrowing, post-capillary proliferation, and interstitial/alveolar hemosiderophages. Biopsies are infrequent because patients often show intolerance or risk of bleeding. PVOD has a dismal prognosis and PAH-targeted drugs are not recommended. Lung transplantation is the most effective treatment. In this article, we present 2 cases of PVOD masquerading as idiopathic pulmonary arterial hypertension (IPAH) and responding well to PAH targeted drugs.
4.246094
0.733398
sec[0]/p[0]
en
0.999998
34731104
https://doi.org/10.1097/MD.0000000000027334
[ "pvod", "pulmonary", "usually", "arterial", "hypertension", "which", "venules", "tissue", "cases", "patients" ]
[ { "code": "CB40.Y", "title": "Other specified diseases of the respiratory system" }, { "code": "LA75.1", "title": "Agenesis of lung" }, { "code": "CA40.Z", "title": "Pneumonia, organism unspecified" }, { "code": "CB41", "title": "Respiratory failure" }, { "code": "NB32.3Y", "title": "Other injury of lung" }, { "code": "LA8Y", "title": "Other specified structural developmental anomaly of heart or great vessels" }, { "code": "2E67.13", "title": "High grade squamous intraepithelial lesion of vulva, HPV-associated" }, { "code": "BD5Z", "title": "Diseases of arteries or arterioles, unspecified" }, { "code": "BD52", "title": "Certain specified disorders of arteries or arterioles" }, { "code": "BD52.3", "title": "Rupture of artery" } ]
=== ICD-11 CODES FOUND === [CB40.Y] Other specified diseases of the respiratory system Also known as: Other specified diseases of the respiratory system | Secondary respiratory disorders | Respiratory disorders in diseases classified elsewhere | Diseases of bronchus, not elsewhere classified | Acquired bronchial diverticulum [LA75.1] Agenesis of lung Definition: This refers to the absence or rudimentary residua of an undeveloped lung. Also known as: Agenesis of lung | Pulmonary agenesis | absence of lung | aplasia of lung | apulmonism [CA40.Z] Pneumonia, organism unspecified Also known as: Pneumonia, organism unspecified | Pneumonia | infectious pneumonia | PN - [pneumonia] | lobar pneumonia NOS [CB41] Respiratory failure Definition: Respiratory failure is a life-threatening impairment of oxygenation or carbon dioxide (CO2) elimination. Respiratory failure may occur because of impaired gas exchange, decreased ventilation, or both. The level of oxygen in the blood becomes dangerously low or the level of carbon dioxide becomes dangerously high. Also known as: Respiratory failure | lung failure NOS | pulmonary failure Excludes: Acute respiratory distress syndrome | Respiratory arrest | Respiratory distress of newborn [NB32.3Y] Other injury of lung Also known as: Other injury of lung | Haematoma of lung | Traumatic hydropneumothorax | Acute traumatic lung congestion | Rupture of lung [LA8Y] Other specified structural developmental anomaly of heart or great vessels Also known as: Other specified structural developmental anomaly of heart or great vessels | Congenital anomaly of position or spatial relationships of thoraco-abdominal organs | Usual atrial arrangement | atrial situs solitus | Abnormal atrial arrangement [2E67.13] High grade squamous intraepithelial lesion of vulva, HPV-associated Definition: Squamous intraepithelial lesions (SILs) of the vulva (also known as vulvar intraepithelial neoplasia [VIN]), HPV-associated, are proliferations of squamous cells driven by HPV infection, showing maturation abnormalities and nuclear hyperchromasia that do not extend beyond the basement membrane. Also known as: High grade squamous intraepithelial lesion of vulva, HPV-associated | Vulvar intraepithelial neoplasia, usual type | Vulvar intraepithelial neoplasia, usual (classical) | VIN III, HPV associated | VIN II, HPV associated [BD5Z] Diseases of arteries or arterioles, unspecified Also known as: Diseases of arteries or arterioles, unspecified | artery disease NOS | arterial disease NOS | arteriolar disease NOS | disorder of artery NOS [BD52] Certain specified disorders of arteries or arterioles Also known as: Certain specified disorders of arteries or arterioles | Aortic dilatation - joint hypermobility - arterial tortuosity | Generalised arterial calcification of infancy | Median arcuate ligament syndrome | Aortic root abscess Excludes: collagen (vascular) diseases | Hypersensitivity angiitis | Acute arterial occlusion [BD52.3] Rupture of artery Also known as: Rupture of artery | ruptured artery | artery fistula | Aortic duodenal fistula | Aortic colon fistula Excludes: traumatic rupture of artery - see injury of blood vessel by body region === GRAPH WALKS === --- Walk 1 --- [CB40.Y] Other specified diseases of the respiratory system --PARENT--> [CB40] Certain diseases of the respiratory system --RELATED_TO--> [?] Airway obstruction in the neonate due to airway abnormality --- Walk 2 --- [CB40.Y] Other specified diseases of the respiratory system --PARENT--> [CB40] Certain diseases of the respiratory system --RELATED_TO--> [?] Airway obstruction in the neonate due to airway abnormality --- Walk 3 --- [LA75.1] Agenesis of lung Def: This refers to the absence or rudimentary residua of an undeveloped lung.... --PARENT--> [LA75] Structural developmental anomalies of lungs Def: Any condition caused by failure of the lungs to correctly develop during the antenatal period.... --CHILD--> [LA75.0] Accessory lobe of lung Def: An extra lobe of lung beyond the 3 on the right and the 2 on the left... --- Walk 4 --- [LA75.1] Agenesis of lung Def: This refers to the absence or rudimentary residua of an undeveloped lung.... --PARENT--> [LA75] Structural developmental anomalies of lungs Def: Any condition caused by failure of the lungs to correctly develop during the antenatal period.... --CHILD--> [LA75.0] Accessory lobe of lung Def: An extra lobe of lung beyond the 3 on the right and the 2 on the left... --- Walk 5 --- [CA40.Z] Pneumonia, organism unspecified --PARENT--> [CA40] Pneumonia Def: A disease of the lungs, frequently but not always caused by an infection with bacteria, virus, fungus, or parasite. This disease is characterised by fever, chills, cough with sputum production, chest ... --RELATED_TO--> [?] Congenital pneumonia Def: Congenital pneumonia is an acute respiratory infection contracted prenatally or during the intrapartum period that is caused by a virus, bacteria, or fungi.... --- Walk 6 --- [CA40.Z] Pneumonia, organism unspecified --PARENT--> [CA40] Pneumonia Def: A disease of the lungs, frequently but not always caused by an infection with bacteria, virus, fungus, or parasite. This disease is characterised by fever, chills, cough with sputum production, chest ... --CHILD--> [CA40.1] Viral pneumonia Def: A disease of the pulmonary system, caused by an infection with a viral source. This disease is characterised by fever, lethargy, headache, myalgia, vomiting, or coughing. Transmission is by inhalation...
[ "[CB40.Y] Other specified diseases of the respiratory system\n --PARENT--> [CB40] Certain diseases of the respiratory system\n --RELATED_TO--> [?] Airway obstruction in the neonate due to airway abnormality", "[CB40.Y] Other specified diseases of the respiratory system\n --PARENT--> [CB40] Certain diseases of the respiratory system\n --RELATED_TO--> [?] Airway obstruction in the neonate due to airway abnormality", "[LA75.1] Agenesis of lung\n Def: This refers to the absence or rudimentary residua of an undeveloped lung....\n --PARENT--> [LA75] Structural developmental anomalies of lungs\n Def: Any condition caused by failure of the lungs to correctly develop during the antenatal period....\n --CHILD--> [LA75.0] Accessory lobe of lung\n Def: An extra lobe of lung beyond the 3 on the right and the 2 on the left...", "[LA75.1] Agenesis of lung\n Def: This refers to the absence or rudimentary residua of an undeveloped lung....\n --PARENT--> [LA75] Structural developmental anomalies of lungs\n Def: Any condition caused by failure of the lungs to correctly develop during the antenatal period....\n --CHILD--> [LA75.0] Accessory lobe of lung\n Def: An extra lobe of lung beyond the 3 on the right and the 2 on the left...", "[CA40.Z] Pneumonia, organism unspecified\n --PARENT--> [CA40] Pneumonia\n Def: A disease of the lungs, frequently but not always caused by an infection with bacteria, virus, fungus, or parasite. This disease is characterised by fever, chills, cough with sputum production, chest ...\n --RELATED_TO--> [?] Congenital pneumonia\n Def: Congenital pneumonia is an acute respiratory infection contracted prenatally or during the intrapartum period that is caused by a virus, bacteria, or fungi....", "[CA40.Z] Pneumonia, organism unspecified\n --PARENT--> [CA40] Pneumonia\n Def: A disease of the lungs, frequently but not always caused by an infection with bacteria, virus, fungus, or parasite. This disease is characterised by fever, chills, cough with sputum production, chest ...\n --CHILD--> [CA40.1] Viral pneumonia\n Def: A disease of the pulmonary system, caused by an infection with a viral source. This disease is characterised by fever, lethargy, headache, myalgia, vomiting, or coughing. Transmission is by inhalation..." ]
CB40.Y
Other specified diseases of the respiratory system
[ { "from_icd11": "LA75.1", "icd10_code": "Q333", "icd10_title": "Agenesis of lung" }, { "from_icd11": "CA40.Z", "icd10_code": "J189", "icd10_title": "Pneumonia, unspecified organism" }, { "from_icd11": "CA40.Z", "icd10_code": "J181", "icd10_title": "Lobar pneumonia, unspecified organism" }, { "from_icd11": "CA40.Z", "icd10_code": "J188", "icd10_title": "Other pneumonia, unspecified organism" }, { "from_icd11": "CA40.Z", "icd10_code": "J168", "icd10_title": "Pneumonia due to other specified infectious organisms" }, { "from_icd11": "CA40.Z", "icd10_code": "J180", "icd10_title": "Bronchopneumonia, unspecified organism" }, { "from_icd11": "CA40.Z", "icd10_code": "J17", "icd10_title": "Pneumonia in diseases classified elsewhere" }, { "from_icd11": "CA40.Z", "icd10_code": "J182", "icd10_title": "Hypostatic pneumonia, unspecified organism" }, { "from_icd11": "CA40.Z", "icd10_code": "J16", "icd10_title": "Pneumonia due to other infectious organisms, not elsewhere classified" }, { "from_icd11": "CA40.Z", "icd10_code": "J171", "icd10_title": "" }, { "from_icd11": "CA40.Z", "icd10_code": "J173", "icd10_title": "" }, { "from_icd11": "CA40.Z", "icd10_code": "J178", "icd10_title": "" }, { "from_icd11": "CA40.Z", "icd10_code": "J18", "icd10_title": "Pneumonia, unspecified organism" }, { "from_icd11": "CB41", "icd10_code": "J9622", "icd10_title": "Acute and chronic respiratory failure with hypercapnia" }, { "from_icd11": "CB41", "icd10_code": "J9620", "icd10_title": "Acute and chronic respiratory failure, unspecified whether with hypoxia or hypercapnia" } ]
Q333
Agenesis of lung
To the best of our knowledge, our finding of a coarcted aneurysm-associated thrombus causing acute renal infarction has not been reported before. This 10-year-old boy presented with fever, rashes, and abdominal pain resulting from renal infarction caused by a coarcted aneurysm. The characteristics of hematuria, proteinuria, hypertension, and rashes on extremities mimic the features of Henoch–Schönlein purpura. Nevertheless, the left costovertebral knocking pain, fever, and elevated serum lactate dehydrogenase and C-reactive protein indicated the possibility of renal infarction ( 3 , 5 , 6 ). An abdominal CT confirmed the diagnosis. Besides thrombolytic or anticoagulant treatment, investigating the underlying etiology should be the focus in order to prevent recurrence of renal infarction. The most common causes of renal infarction are cardiogenic, including arrhythmia, cardiomyopathy, valvular heart diseases, and thrombi from the suprarenal aorta or left ventricle followed by renal artery injury and hypercoagulable state ( 6 , 7 ). Diagnostic testings including intra-cardiac diseases, hypercoagulable conditions, rheumatologic diseases, and images for the vascular abnormalities are essential for uncovering the underlying etiology. Computed tomographic angiogram demonstrated a descending aortic coarctation-associated aneurysm and complicated intra-aneurysmal mural thrombus formation with ulceration.
4.09375
0.929688
sec[2]/p[0]
en
0.999994
34422730
https://doi.org/10.3389/fped.2021.707560
[ "renal", "infarction", "aneurysm", "diseases", "coarcted", "associated", "thrombus", "fever", "rashes", "abdominal" ]
[ { "code": "GC2Z&XA6KU8", "title": "Disease of kidney, not elsewhere classified" }, { "code": "GB6Z", "title": "Kidney failure, unspecified" }, { "code": "LB30.1", "title": "Renal dysplasia" }, { "code": "NB92.0Y", "title": "Other specified injury of kidney" }, { "code": "LB30.7", "title": "Ectopic or pelvic kidney" }, { "code": "FB32.2Z", "title": "Ischaemic infarction of muscle, unspecified" }, { "code": "DD30.Z", "title": "Acute vascular disorders of intestine, unspecified" }, { "code": "8B26.Y", "title": "Other specified vascular syndromes of brain in cerebrovascular diseases" }, { "code": "GB90.3", "title": "Ischaemia or infarction of kidney" }, { "code": "DB98.0", "title": "Infarction of liver" } ]
=== ICD-11 CODES FOUND === [GB6Z] Kidney failure, unspecified Also known as: Kidney failure, unspecified | nontraumatic kidney injury | renal failure NOS | kidney block | renal impairment NOS [LB30.1] Renal dysplasia Definition: A condition characterised by abnormal development of one or both kidneys. Also known as: Renal dysplasia | congenital renal dysplasia | dysplasia of kidney | dysplastic kidney | Primary renal dysplasia Excludes: Autosomal dominant polycystic kidney disease [NB92.0Y] Other specified injury of kidney Also known as: Other specified injury of kidney | Injury of kidney without open wound into cavity | Injury of kidney with open wound into cavity | Haematoma of kidney | traumatic perirenal haematoma [LB30.7] Ectopic or pelvic kidney Definition: A birth defect characterised by an abnormally positioned kidney; may be asymptomatic or result in urine blockage, infection or kidney stones Also known as: Ectopic or pelvic kidney | Congenital displaced kidney | congenital misplaced kidney | congenital malposition of kidney | congenital prolapsed kidney Includes: Congenital displaced kidney | Malrotation of kidney [FB32.2Z] Ischaemic infarction of muscle, unspecified Also known as: Ischaemic infarction of muscle, unspecified | Ischaemic infarction of muscle | muscle infarction [DD30.Z] Acute vascular disorders of intestine, unspecified Also known as: Acute vascular disorders of intestine, unspecified | Acute vascular disorders of intestine | acute intestinal ischemia NOS | acute intestinal ischemic syndrome | acute ischaemic bowel disease [8B26.Y] Other specified vascular syndromes of brain in cerebrovascular diseases Also known as: Other specified vascular syndromes of brain in cerebrovascular diseases | Subcortical ischaemic stroke | subcortical infarction | Cortical ischaemic stroke | cortical infarction [GB90.3] Ischaemia or infarction of kidney Also known as: Ischaemia or infarction of kidney | Complete arterial ischaemia or infarction of kidney | Complete arterial ischaemia or infarction of kidney due to renal artery obstruction | obstructed renal artery | renal artery clot Excludes: Atherosclerosis of renal artery | Goldblatt kidney | Congenital renal artery stenosis [DB98.0] Infarction of liver Definition: Infarction of the liver is hepatic damage caused by limited blood supply to the liver due to obstruction or reduced blood flow of hepatic artery, portal vein or both. Also known as: Infarction of liver | hepatic infarct | hepatic infarction | liver infarct | liver infarction === GRAPH WALKS === --- Walk 1 --- [GB6Z] Kidney failure, unspecified --PARENT--> [?] Kidney failure Def: Inability of the kidneys to adequately filter the blood of waste products, with a lower than normal glomerular filtration rate (GFR). Can be abrupt and potentially reversible (acute kidney injury) or ... --RELATED_TO--> [?] Renal failure following abortion, ectopic or molar pregnancy --- Walk 2 --- [GB6Z] Kidney failure, unspecified --PARENT--> [?] Kidney failure Def: Inability of the kidneys to adequately filter the blood of waste products, with a lower than normal glomerular filtration rate (GFR). Can be abrupt and potentially reversible (acute kidney injury) or ... --EXCLUDES--> [?] Hypertensive renal disease Def: Hypertensive renal disease is a medical condition referring to damage to the kidney due to chronic high blood pressure.... --- Walk 3 --- [LB30.1] Renal dysplasia Def: A condition characterised by abnormal development of one or both kidneys.... --PARENT--> [LB30] Structural developmental anomalies of kidneys Def: Any condition caused by failure of the kidneys to correctly develop during the antenatal period.... --CHILD--> [LB30.2] Congenital single renal cyst Def: A single cyst in a kidney, noted in utero or from birth. No other structural abnormality of the kidney or urinary tract noted.... --- Walk 4 --- [LB30.1] Renal dysplasia Def: A condition characterised by abnormal development of one or both kidneys.... --EXCLUDES--> [?] Autosomal dominant polycystic kidney disease Def: Multiple cysts in both kidneys increasing in number and size from adolescence, associated with development of hypertension and chronic renal failure. Autosomal dominant familial pattern is usual and d... --PARENT--> [?] Hereditary cystic or dysplastic kidney disease, dominant inheritance Def: Cystic or dysplastic renal diseases that are inherited in an autosomal dominant fashion. Usually monogenetic, and can be associated with abnormalities in other organs.... --- Walk 5 --- [NB92.0Y] Other specified injury of kidney --PARENT--> [NB92.0] Injury of kidney --CHILD--> [NB92.00] Contusion of kidney, minor --- Walk 6 --- [NB92.0Y] Other specified injury of kidney --PARENT--> [NB92.0] Injury of kidney --PARENT--> [NB92] Injury of urinary or pelvic organs
[ "[GB6Z] Kidney failure, unspecified\n --PARENT--> [?] Kidney failure\n Def: Inability of the kidneys to adequately filter the blood of waste products, with a lower than normal glomerular filtration rate (GFR). Can be abrupt and potentially reversible (acute kidney injury) or ...\n --RELATED_TO--> [?] Renal failure following abortion, ectopic or molar pregnancy", "[GB6Z] Kidney failure, unspecified\n --PARENT--> [?] Kidney failure\n Def: Inability of the kidneys to adequately filter the blood of waste products, with a lower than normal glomerular filtration rate (GFR). Can be abrupt and potentially reversible (acute kidney injury) or ...\n --EXCLUDES--> [?] Hypertensive renal disease\n Def: Hypertensive renal disease is a medical condition referring to damage to the kidney due to chronic high blood pressure....", "[LB30.1] Renal dysplasia\n Def: A condition characterised by abnormal development of one or both kidneys....\n --PARENT--> [LB30] Structural developmental anomalies of kidneys\n Def: Any condition caused by failure of the kidneys to correctly develop during the antenatal period....\n --CHILD--> [LB30.2] Congenital single renal cyst\n Def: A single cyst in a kidney, noted in utero or from birth. No other structural abnormality of the kidney or urinary tract noted....", "[LB30.1] Renal dysplasia\n Def: A condition characterised by abnormal development of one or both kidneys....\n --EXCLUDES--> [?] Autosomal dominant polycystic kidney disease\n Def: Multiple cysts in both kidneys increasing in number and size from adolescence, associated with development of hypertension and chronic renal failure. Autosomal dominant familial pattern is usual and d...\n --PARENT--> [?] Hereditary cystic or dysplastic kidney disease, dominant inheritance\n Def: Cystic or dysplastic renal diseases that are inherited in an autosomal dominant fashion. Usually monogenetic, and can be associated with abnormalities in other organs....", "[NB92.0Y] Other specified injury of kidney\n --PARENT--> [NB92.0] Injury of kidney\n --CHILD--> [NB92.00] Contusion of kidney, minor", "[NB92.0Y] Other specified injury of kidney\n --PARENT--> [NB92.0] Injury of kidney\n --PARENT--> [NB92] Injury of urinary or pelvic organs" ]
GC2Z&XA6KU8
Disease of kidney, not elsewhere classified
[ { "from_icd11": "GB6Z", "icd10_code": "N19", "icd10_title": "Unspecified kidney failure" }, { "from_icd11": "GB6Z", "icd10_code": "N17-N19", "icd10_title": "" }, { "from_icd11": "GB6Z", "icd10_code": "N17", "icd10_title": "Acute kidney failure" }, { "from_icd11": "LB30.1", "icd10_code": "Q614", "icd10_title": "Renal dysplasia" }, { "from_icd11": "LB30.7", "icd10_code": "Q632", "icd10_title": "Ectopic kidney" }, { "from_icd11": "LB30.7", "icd10_code": "Q63", "icd10_title": "Other congenital malformations of kidney" }, { "from_icd11": "FB32.2Z", "icd10_code": "M62261", "icd10_title": "Nontraumatic ischemic infarction of muscle, right lower leg" }, { "from_icd11": "FB32.2Z", "icd10_code": "M62252", "icd10_title": "Nontraumatic ischemic infarction of muscle, left thigh" }, { "from_icd11": "FB32.2Z", "icd10_code": "M62251", "icd10_title": "Nontraumatic ischemic infarction of muscle, right thigh" }, { "from_icd11": "FB32.2Z", "icd10_code": "M62242", "icd10_title": "Nontraumatic ischemic infarction of muscle, left hand" }, { "from_icd11": "FB32.2Z", "icd10_code": "M6220", "icd10_title": "Nontraumatic ischemic infarction of muscle, unspecified site" }, { "from_icd11": "FB32.2Z", "icd10_code": "M622", "icd10_title": "Nontraumatic ischemic infarction of muscle" }, { "from_icd11": "DD30.Z", "icd10_code": "K55019", "icd10_title": "Acute (reversible) ischemia of small intestine, extent unspecified" }, { "from_icd11": "DD30.Z", "icd10_code": "K55029", "icd10_title": "Acute infarction of small intestine, extent unspecified" }, { "from_icd11": "DD30.Z", "icd10_code": "K55069", "icd10_title": "Acute infarction of intestine, part and extent unspecified" } ]
N19
Unspecified kidney failure
Two months after her discharge, the patient again presented to the ED after being found to have hypotension and hypoxia by a visiting nurse. She reported feeling chills, weakness, fatigue, and dizziness since April, which had become worse two days prior to the admission. She denied symptoms of flank pain, dysuria, hematuria, or urinary frequency. On presentation, the patient was afebrile, hypotensive at 83/61 mmHg, and tachycardic at 112 beats per minute. Physical exam was positive for bilateral costovertebral angle (CVA) tenderness. Labs were significant for brain natriuretic peptide (BNP) of 1,341 pg/mL, creatinine of 0.7 mg/dL (baseline: 0.3 mg/dL), troponin of 0.47 ng/mL, corrected calcium of 12.1 mg/dL, PTH of 371 pg/mL, erythrocyte sedimentation rate (ESR) of 82 mm/hr, C-reactive protein (CRP) of 192 mg/L, hypokalemia at K 2.8 mEq/L, and hypomagnesemia at 1.4 mg/dL. Blood culture grew Enterococcus faecalis (Table 1 ). Urinalysis showed moderate leukocyte esterase, WBC of 106/HPF, and RBC of 11/HPF (Table 1 ). Urine culture grew mixed flora with a colony count between 10,000 CFU/MI and 100,000 CFU/MI. Transabdominal ultrasound of kidneys and urinary bladder revealed multiple stones in the right kidney, left kidney, and left ureterovesical junction . CT abdomen/pelvis without IV contrast showed renal stones in the lower pole of bilateral kidneys and fullness of both renal collecting systems .
3.861328
0.980469
sec[1]/p[1]
en
0.999998
PMC8893220
https://doi.org/10.7759/cureus.21788
[ "urinary", "culture", "grew", "kidneys", "stones", "kidney", "renal", "hypotension", "hypoxia", "visiting" ]
[ { "code": "GB6Z", "title": "Kidney failure, unspecified" }, { "code": "GC04.Z", "title": "Fistula of the genitourinary tract, unspecified" }, { "code": "MF51", "title": "Anuria or oliguria" }, { "code": "GB70.Z", "title": "Calculus of upper urinary tract, unspecified" }, { "code": "GC2Z", "title": "Diseases of the urinary system, unspecified" }, { "code": "QE00", "title": "Acculturation difficulty" }, { "code": "MD40.51", "title": "Positive sputum culture" }, { "code": "MD40.52", "title": "Positive throat culture" }, { "code": "QE0Z", "title": "Problems associated with social or cultural environment, unspecified" }, { "code": "MG65", "title": "Abnormal microbiological findings in specimens from other organs, systems and tissues" } ]
=== ICD-11 CODES FOUND === [GB6Z] Kidney failure, unspecified Also known as: Kidney failure, unspecified | nontraumatic kidney injury | renal failure NOS | kidney block | renal impairment NOS [GC04.Z] Fistula of the genitourinary tract, unspecified Also known as: Fistula of the genitourinary tract, unspecified | Fistula of the genitourinary tract | persistent urinary fistula | persistent urinary tract fistula | recurrent urinary fistula [MF51] Anuria or oliguria Definition: Anuria means nonpassage of urine, in practice is defined as passage of less than 50 millilitres of urine in a day. Oliguria is the low output of urine. It is clinically classified as an output below 300-500ml/day. Also known as: Anuria or oliguria | Anuria | suppression of urinary secretion | ischuria | Oliguria Excludes: Maternal care for other conditions predominantly related to pregnancy [GB70.Z] Calculus of upper urinary tract, unspecified Also known as: Calculus of upper urinary tract, unspecified | Calculus of upper urinary tract | calculus of urinary tract NOS | urinary calculi | urinary calculus, unspecified [GC2Z] Diseases of the urinary system, unspecified Also known as: Diseases of the urinary system, unspecified | urinary tract disease NOS | Abnormal renal function | kidney dysfunction NOS | kidney hypofunction [QE00] Acculturation difficulty Definition: Problems resulting from the inability to adjust to a different culture or environment. Also known as: Acculturation difficulty | acculturation problem | cultural shock | social migrant difficulty | migration Excludes: Disorders specifically associated with stress [MD40.51] Positive sputum culture Also known as: Positive sputum culture [MD40.52] Positive throat culture Also known as: Positive throat culture [QE0Z] Problems associated with social or cultural environment, unspecified Also known as: Problems associated with social or cultural environment, unspecified | social environment problem [MG65] Abnormal microbiological findings in specimens from other organs, systems and tissues Also known as: Abnormal microbiological findings in specimens from other organs, systems and tissues | positive wound culture | Positive culture findings on specimen from other organs, systems and tissue === GRAPH WALKS === --- Walk 1 --- [GB6Z] Kidney failure, unspecified --PARENT--> [?] Kidney failure Def: Inability of the kidneys to adequately filter the blood of waste products, with a lower than normal glomerular filtration rate (GFR). Can be abrupt and potentially reversible (acute kidney injury) or ... --RELATED_TO--> [?] Congenital renal failure Def: A severe irreversible decline in the ability of kidneys to remove wastes, concentrate urine, and maintain electrolyte balance; blood pressure; and calcium metabolism which existed at, or often before,... --- Walk 2 --- [GB6Z] Kidney failure, unspecified --PARENT--> [?] Kidney failure Def: Inability of the kidneys to adequately filter the blood of waste products, with a lower than normal glomerular filtration rate (GFR). Can be abrupt and potentially reversible (acute kidney injury) or ... --RELATED_TO--> [?] Congenital renal failure Def: A severe irreversible decline in the ability of kidneys to remove wastes, concentrate urine, and maintain electrolyte balance; blood pressure; and calcium metabolism which existed at, or often before,... --- Walk 3 --- [GC04.Z] Fistula of the genitourinary tract, unspecified --PARENT--> [GC04] Fistula of the genitourinary tract Def: Any condition caused by trauma, medical intervention, infection, cancer, or congenital factors. This condition is characterised by the formation of an abnormal passage between any two locations within... --CHILD--> [GC04.1] Fistulae involving female genital tract Def: Any condition characterised by the formation of an abnormal passage between the genital tract and another organ, or between a genital organ and an adjacent organ or surface.... --- Walk 4 --- [GC04.Z] Fistula of the genitourinary tract, unspecified --PARENT--> [GC04] Fistula of the genitourinary tract Def: Any condition caused by trauma, medical intervention, infection, cancer, or congenital factors. This condition is characterised by the formation of an abnormal passage between any two locations within... --CHILD--> [GC04.2] Ureteral fistula Def: Abnormal passage or communication between the ureter and another body organ or cavity or the body surface.... --- Walk 5 --- [MF51] Anuria or oliguria Def: Anuria means nonpassage of urine, in practice is defined as passage of less than 50 millilitres of urine in a day. Oliguria is the low output of urine. It is clinically classified as an output below 3... --EXCLUDES--> [?] Maternal care for other conditions predominantly related to pregnancy Def: Any reason for encounter to assess (or care for) a mother for other conditions predominantly related to pregnancy.... --CHILD--> [?] Pregnancy dermatoses Def: A group of skin disorders which are specific to pregnancy.... --- Walk 6 --- [MF51] Anuria or oliguria Def: Anuria means nonpassage of urine, in practice is defined as passage of less than 50 millilitres of urine in a day. Oliguria is the low output of urine. It is clinically classified as an output below 3... --EXCLUDES--> [?] Maternal care for other conditions predominantly related to pregnancy Def: Any reason for encounter to assess (or care for) a mother for other conditions predominantly related to pregnancy.... --PARENT--> [?] Certain specified maternal disorders predominantly related to pregnancy Def: A group of conditions of the mother which occur during the period of time from conception to delivery (pregnancy)....
[ "[GB6Z] Kidney failure, unspecified\n --PARENT--> [?] Kidney failure\n Def: Inability of the kidneys to adequately filter the blood of waste products, with a lower than normal glomerular filtration rate (GFR). Can be abrupt and potentially reversible (acute kidney injury) or ...\n --RELATED_TO--> [?] Congenital renal failure\n Def: A severe irreversible decline in the ability of kidneys to remove wastes, concentrate urine, and maintain electrolyte balance; blood pressure; and calcium metabolism which existed at, or often before,...", "[GB6Z] Kidney failure, unspecified\n --PARENT--> [?] Kidney failure\n Def: Inability of the kidneys to adequately filter the blood of waste products, with a lower than normal glomerular filtration rate (GFR). Can be abrupt and potentially reversible (acute kidney injury) or ...\n --RELATED_TO--> [?] Congenital renal failure\n Def: A severe irreversible decline in the ability of kidneys to remove wastes, concentrate urine, and maintain electrolyte balance; blood pressure; and calcium metabolism which existed at, or often before,...", "[GC04.Z] Fistula of the genitourinary tract, unspecified\n --PARENT--> [GC04] Fistula of the genitourinary tract\n Def: Any condition caused by trauma, medical intervention, infection, cancer, or congenital factors. This condition is characterised by the formation of an abnormal passage between any two locations within...\n --CHILD--> [GC04.1] Fistulae involving female genital tract\n Def: Any condition characterised by the formation of an abnormal passage between the genital tract and another organ, or between a genital organ and an adjacent organ or surface....", "[GC04.Z] Fistula of the genitourinary tract, unspecified\n --PARENT--> [GC04] Fistula of the genitourinary tract\n Def: Any condition caused by trauma, medical intervention, infection, cancer, or congenital factors. This condition is characterised by the formation of an abnormal passage between any two locations within...\n --CHILD--> [GC04.2] Ureteral fistula\n Def: Abnormal passage or communication between the ureter and another body organ or cavity or the body surface....", "[MF51] Anuria or oliguria\n Def: Anuria means nonpassage of urine, in practice is defined as passage of less than 50 millilitres of urine in a day. Oliguria is the low output of urine. It is clinically classified as an output below 3...\n --EXCLUDES--> [?] Maternal care for other conditions predominantly related to pregnancy\n Def: Any reason for encounter to assess (or care for) a mother for other conditions predominantly related to pregnancy....\n --CHILD--> [?] Pregnancy dermatoses\n Def: A group of skin disorders which are specific to pregnancy....", "[MF51] Anuria or oliguria\n Def: Anuria means nonpassage of urine, in practice is defined as passage of less than 50 millilitres of urine in a day. Oliguria is the low output of urine. It is clinically classified as an output below 3...\n --EXCLUDES--> [?] Maternal care for other conditions predominantly related to pregnancy\n Def: Any reason for encounter to assess (or care for) a mother for other conditions predominantly related to pregnancy....\n --PARENT--> [?] Certain specified maternal disorders predominantly related to pregnancy\n Def: A group of conditions of the mother which occur during the period of time from conception to delivery (pregnancy)...." ]
GB6Z
Kidney failure, unspecified
[ { "from_icd11": "GB6Z", "icd10_code": "N19", "icd10_title": "Unspecified kidney failure" }, { "from_icd11": "GB6Z", "icd10_code": "N17-N19", "icd10_title": "" }, { "from_icd11": "GB6Z", "icd10_code": "N17", "icd10_title": "Acute kidney failure" }, { "from_icd11": "GC04.Z", "icd10_code": "N321", "icd10_title": "Vesicointestinal fistula" }, { "from_icd11": "MF51", "icd10_code": "R34", "icd10_title": "Anuria and oliguria" }, { "from_icd11": "GB70.Z", "icd10_code": "N202", "icd10_title": "Calculus of kidney with calculus of ureter" }, { "from_icd11": "GB70.Z", "icd10_code": "N209", "icd10_title": "Urinary calculus, unspecified" }, { "from_icd11": "GB70.Z", "icd10_code": "N20", "icd10_title": "Calculus of kidney and ureter" }, { "from_icd11": "QE00", "icd10_code": "Z603", "icd10_title": "Acculturation difficulty" }, { "from_icd11": "QE0Z", "icd10_code": "Z7389", "icd10_title": "Other problems related to life management difficulty" }, { "from_icd11": "QE0Z", "icd10_code": "Z7382", "icd10_title": "Dual sensory impairment" }, { "from_icd11": "QE0Z", "icd10_code": "Z608", "icd10_title": "Other problems related to social environment" }, { "from_icd11": "QE0Z", "icd10_code": "Z609", "icd10_title": "Problem related to social environment, unspecified" }, { "from_icd11": "QE0Z", "icd10_code": "Z60", "icd10_title": "Problems related to social environment" }, { "from_icd11": "QE0Z", "icd10_code": "Z73", "icd10_title": "Problems related to life management difficulty" } ]
N19
Unspecified kidney failure
A 15-year-old previously healthy male with no significant past medical history presented to the emergency department for bleeding left scapular mass. He initially noticed the lesion two weeks before the presentation. The mass ruptured due to leaning against the wall. He was brought to the hospital by his parents due to continued bleeding. He denied any pain from the area except shortly after it ruptured. There was no history of fever, night sweats, weight loss, chills, appetite changes, and numbness to the site. Clinical examination revealed a non-purulent, solitary, and well-circumscribed mass located on the skin overlying the lateral side of the left scapula, measuring about 2.5 x 3 cm. On palpation, the mass was firm and non-tender with a fluctuant inferior surface. Excoriations and scabs were also noticed on the mass . The rest of the examination was unremarkable. Baseline investigations, including the complete blood count and basic metabolic panel, were normal. Ultrasound findings were suggestive of neoplasm, and contrast-enhanced MRI was recommended for further evaluation . Initial differentials included cyst versus abscess versus neoplasm. MRI findings were highly suspicious for progressive neoplasm . We consulted the surgical team, and the mass's surgical excision was carried out. Biopsy of the mass confirmed pilomatrixoma . On one year follow-up, no recurrence of the lesion was observed.
3.708984
0.987793
sec[1]/p[0]
en
0.999995
34168921
https://doi.org/10.7759/cureus.15135
[ "neoplasm", "bleeding", "noticed", "lesion", "ruptured", "versus", "previously", "healthy", "past", "emergency" ]
[ { "code": "2F9Z", "title": "Neoplasms of unknown behaviour of unspecified site" }, { "code": "ME61", "title": "Subcutaneous swelling, mass or lump of uncertain or unspecified nature" }, { "code": "2E6Z", "title": "Carcinoma in situ of unspecified site" }, { "code": "2F91.1", "title": "Neoplasms of unknown behaviour of trachea, bronchus or lung" }, { "code": "2F92", "title": "Neoplasms of unknown behaviour of skin" }, { "code": "MG27", "title": "Haemorrhage, not elsewhere classified" }, { "code": "GA21.0", "title": "Postcoital or contact bleeding" }, { "code": "MF50.4Z", "title": "Haematuria, unspecified" }, { "code": "DB98.A", "title": "Hepatic haemorrhage" }, { "code": "GA20.3", "title": "Abnormal regularity of uterine bleeding" } ]
=== ICD-11 CODES FOUND === [2F9Z] Neoplasms of unknown behaviour of unspecified site Also known as: Neoplasms of unknown behaviour of unspecified site | neoplasia | neoplasm growth NOS | tumour of unspecified site | tumourlet of unspecified site [ME61] Subcutaneous swelling, mass or lump of uncertain or unspecified nature Definition: One or more localised subcutaneous soft tissue masses of undetermined or unspecified nature Also known as: Subcutaneous swelling, mass or lump of uncertain or unspecified nature | localised swelling, mass or lump of skin and subcutaneous tissue | localised subcutaneous nodules | subcutaneous nodules | superficial subcutaneous nodules Excludes: localized adiposity | mass and lump: breast | enlarged lymph nodes [2E6Z] Carcinoma in situ of unspecified site Also known as: Carcinoma in situ of unspecified site | carcinoma in situ of unspecified site | carcinoma in situ NOS | carcinoma in situ | in situ neoplasm [2F91.1] Neoplasms of unknown behaviour of trachea, bronchus or lung Also known as: Neoplasms of unknown behaviour of trachea, bronchus or lung | trachea, bronchus or lung tumour NOS | Intravascular bronchial alveolar tumour of unspecified site | Bronchial adenoma of unknown behaviour of unspecified site | Intravascular bronchial alveolar tumour unknown behaviour of unspecified site [2F92] Neoplasms of unknown behaviour of skin Also known as: Neoplasms of unknown behaviour of skin | skin tumour NOS [MG27] Haemorrhage, not elsewhere classified Definition: Bleeding or escape of blood from a vessel. Also known as: Haemorrhage, not elsewhere classified | arterial haemorrhage | bleeding | extravasation of blood | Haemorrhage NOS Excludes: Obstetric haemorrhage | Haemorrhage or haematoma complicating a procedure, not elsewhere classified | Fetal blood loss [GA21.0] Postcoital or contact bleeding Definition: A condition of the genital system, caused by infection, cervical ectropion, cervical or endometrial polyps, cancer, or trauma to the cervix or vagina. This condition is characterised by non-menstrual bleeding after sexual intercourse. Confirmation is by transvaginal imaging to identify any structural abnormalities. Also known as: Postcoital or contact bleeding | Postcoital bleeding | bleeding after intercourse | PCB - [postcoital bleeding] | postcoital haemorrhage [MF50.4Z] Haematuria, unspecified Also known as: Haematuria, unspecified | Haematuria | blood in urine | urinary blood | haematuria NOS [DB98.A] Hepatic haemorrhage Definition: Traumatic or nontraumatic spontaneous bleeding in the liver. The most common cause of the latter is the rupture of liver tumours. Also known as: Hepatic haemorrhage | haemorrhage of liver | hepatic bleeding | hepatorrhagia | liver haemorrhage Excludes: Hepatic haemorrhage due to hepatocellular carcinoma [GA20.3] Abnormal regularity of uterine bleeding Definition: A condition of the genital system affecting females, caused by hormonal disturbances. This condition is characterised by abnormal menstruation, with a between cycle variation of 2-20 days. Also known as: Abnormal regularity of uterine bleeding | Irregular menstrual bleeding | irregular cycle menstruation | irregular menses | irregular menstrual cycle === GRAPH WALKS === --- Walk 1 --- [2F9Z] Neoplasms of unknown behaviour of unspecified site --PARENT--> [?] Neoplasms of unknown behaviour, except of lymphoid, haematopoietic, central nervous system or related tissues --PARENT--> [02] Neoplasms Def: An abnormal or uncontrolled cellular proliferation which is not coordinated with an organism's requirements for normal tissue growth, replacement or repair.... --- Walk 2 --- [2F9Z] Neoplasms of unknown behaviour of unspecified site --PARENT--> [?] Neoplasms of unknown behaviour, except of lymphoid, haematopoietic, central nervous system or related tissues --RELATED_TO--> [?] Pathological fracture in neoplastic disease of unknown behaviour --- Walk 3 --- [ME61] Subcutaneous swelling, mass or lump of uncertain or unspecified nature Def: One or more localised subcutaneous soft tissue masses of undetermined or unspecified nature... --EXCLUDES--> [?] Localised adiposity Def: A condition characterised by accumulation of adipose tissue in specific regions of the body.... --CHILD--> [?] Fatty apron --- Walk 4 --- [ME61] Subcutaneous swelling, mass or lump of uncertain or unspecified nature Def: One or more localised subcutaneous soft tissue masses of undetermined or unspecified nature... --PARENT--> [?] Symptoms or signs involving the skin Def: This category allows the capture of imprecise data where a more specific diagnosis cannot be made or to supplement information about a specific diagnosis.... --CHILD--> [ME60] Skin lesion of uncertain or unspecified nature Def: To be used where there is either significant uncertainty or alternatively no information as to the nature of a circumscribed skin lesion. This is of particular importance with regard to whether or not... --- Walk 5 --- [2E6Z] Carcinoma in situ of unspecified site --PARENT--> [?] In situ neoplasms, except of lymphoid, haematopoietic, central nervous system or related tissues --CHILD--> [2E61] Carcinoma in situ of other or unspecified digestive organs --- Walk 6 --- [2E6Z] Carcinoma in situ of unspecified site --PARENT--> [?] In situ neoplasms, except of lymphoid, haematopoietic, central nervous system or related tissues --CHILD--> [2E62] Carcinoma in situ of middle ear or respiratory system
[ "[2F9Z] Neoplasms of unknown behaviour of unspecified site\n --PARENT--> [?] Neoplasms of unknown behaviour, except of lymphoid, haematopoietic, central nervous system or related tissues\n --PARENT--> [02] Neoplasms\n Def: An abnormal or uncontrolled cellular proliferation which is not coordinated with an organism's requirements for normal tissue growth, replacement or repair....", "[2F9Z] Neoplasms of unknown behaviour of unspecified site\n --PARENT--> [?] Neoplasms of unknown behaviour, except of lymphoid, haematopoietic, central nervous system or related tissues\n --RELATED_TO--> [?] Pathological fracture in neoplastic disease of unknown behaviour", "[ME61] Subcutaneous swelling, mass or lump of uncertain or unspecified nature\n Def: One or more localised subcutaneous soft tissue masses of undetermined or unspecified nature...\n --EXCLUDES--> [?] Localised adiposity\n Def: A condition characterised by accumulation of adipose tissue in specific regions of the body....\n --CHILD--> [?] Fatty apron", "[ME61] Subcutaneous swelling, mass or lump of uncertain or unspecified nature\n Def: One or more localised subcutaneous soft tissue masses of undetermined or unspecified nature...\n --PARENT--> [?] Symptoms or signs involving the skin\n Def: This category allows the capture of imprecise data where a more specific diagnosis cannot be made or to supplement information about a specific diagnosis....\n --CHILD--> [ME60] Skin lesion of uncertain or unspecified nature\n Def: To be used where there is either significant uncertainty or alternatively no information as to the nature of a circumscribed skin lesion. This is of particular importance with regard to whether or not...", "[2E6Z] Carcinoma in situ of unspecified site\n --PARENT--> [?] In situ neoplasms, except of lymphoid, haematopoietic, central nervous system or related tissues\n --CHILD--> [2E61] Carcinoma in situ of other or unspecified digestive organs", "[2E6Z] Carcinoma in situ of unspecified site\n --PARENT--> [?] In situ neoplasms, except of lymphoid, haematopoietic, central nervous system or related tissues\n --CHILD--> [2E62] Carcinoma in situ of middle ear or respiratory system" ]
2F9Z
Neoplasms of unknown behaviour of unspecified site
[ { "from_icd11": "2F9Z", "icd10_code": "D487", "icd10_title": "Neoplasm of uncertain behavior of other specified sites" }, { "from_icd11": "2F9Z", "icd10_code": "D482", "icd10_title": "Neoplasm of uncertain behavior of peripheral nerves and autonomic nervous system" }, { "from_icd11": "2F9Z", "icd10_code": "D37-D48", "icd10_title": "" }, { "from_icd11": "2F9Z", "icd10_code": "D377", "icd10_title": "" }, { "from_icd11": "2F9Z", "icd10_code": "D48", "icd10_title": "Neoplasm of uncertain behavior of other and unspecified sites" }, { "from_icd11": "2F9Z", "icd10_code": "D489", "icd10_title": "Neoplasm of uncertain behavior, unspecified" }, { "from_icd11": "ME61", "icd10_code": "R2240", "icd10_title": "Localized swelling, mass and lump, unspecified lower limb" }, { "from_icd11": "ME61", "icd10_code": "R2232", "icd10_title": "Localized swelling, mass and lump, left upper limb" }, { "from_icd11": "ME61", "icd10_code": "R2242", "icd10_title": "Localized swelling, mass and lump, left lower limb" }, { "from_icd11": "ME61", "icd10_code": "R2231", "icd10_title": "Localized swelling, mass and lump, right upper limb" }, { "from_icd11": "ME61", "icd10_code": "R2241", "icd10_title": "Localized swelling, mass and lump, right lower limb" }, { "from_icd11": "ME61", "icd10_code": "R2233", "icd10_title": "Localized swelling, mass and lump, upper limb, bilateral" }, { "from_icd11": "ME61", "icd10_code": "R2243", "icd10_title": "Localized swelling, mass and lump, lower limb, bilateral" }, { "from_icd11": "ME61", "icd10_code": "R2230", "icd10_title": "Localized swelling, mass and lump, unspecified upper limb" }, { "from_icd11": "ME61", "icd10_code": "R220", "icd10_title": "Localized swelling, mass and lump, head" } ]
D487
Neoplasm of uncertain behavior of other specified sites
A 76-year old man presented with a four month history of penile pain and erythema to the urology department. Symptom progression over the preceding months included burning with urination and difficulty retracting foreskin. Initial treatment with a two-week course of nystatin-triamcinolone cream was unsuccessful. Physical exam demonstrated a two-centimeter large fungating mass on the ventral surface of the distal shaft, which appeared to originate from the glans. Digital rectal exam revealed an enlarged, firm, and nodular prostate. The remainder of the physical exam was within normal limits. There was no palpable lymphadenopathy, no focal spinal tenderness, and a normal neurological exam without focal or gross motor weakness. Given the suspicious features of the mass for SCC, particularly the fungating and superficial nature, a discussion with the patient was made regarding management options including biopsy for definitive diagnosis versus partial penectomy. The patient opted for surgical treatment and tolerated surgery well. Pathology following treatment demonstrated Gleason 9 prostate cancer. CT scan of the pelvis was performed following penectomy to assess treatment response, and demonstrated a stable sclerotic lesion on the iliac bone with potential sclerosis inferior to this known lesion and no lymphadenopathy. Bone scan at this time demonstrated no definitive evidence of metastatic disease.
3.753906
0.98584
sec[1]/p[0]
en
0.999998
34430213
https://doi.org/10.1016/j.eucr.2021.101804
[ "exam", "physical", "fungating", "prostate", "lymphadenopathy", "definitive", "penectomy", "scan", "lesion", "bone" ]
[ { "code": "6B03", "title": "Specific phobia" }, { "code": "MG44.1Z", "title": "Lack of expected normal physiological development, unspecified" }, { "code": "PJ20", "title": "Physical maltreatment" }, { "code": "MB23.0", "title": "Aggressive behaviour" }, { "code": "QD70.Z", "title": "Problems associated with the natural environment or human-made changes to the environment, unspecified" }, { "code": "QE82.0", "title": "Personal history of physical abuse" }, { "code": "GA90", "title": "Hyperplasia of prostate" }, { "code": "GA91.Z", "title": "Inflammatory or other diseases of prostate, unspecified" }, { "code": "GA91.Y", "title": "Other specified inflammatory or other diseases of prostate" }, { "code": "GA91.0", "title": "Chronic prostatitis" } ]
=== ICD-11 CODES FOUND === [6B03] Specific phobia Definition: Specific phobia is characterised by a marked and excessive fear or anxiety that consistently occurs upon exposure or anticipation of exposure to one or more specific objects or situations (e.g., proximity to certain animals, flying, heights, closed spaces, sight of blood or injury) that is out of proportion to actual danger. The phobic objects or situations are avoided or else endured with intense fear or anxiety. Symptoms persist for at least several months and are sufficiently severe to result Also known as: Specific phobia | Simple phobia | isolated phobia | Acarophobia | Acrophobia Includes: Simple phobia Excludes: Body dysmorphic disorder | Hypochondriasis [MG44.1Z] Lack of expected normal physiological development, unspecified Also known as: Lack of expected normal physiological development, unspecified | Lack of expected normal physiological development | delayed physiological development | unspecified delay in development | development arrest [PJ20] Physical maltreatment Definition: Non-accidental acts of physical force that result, or have reasonable potential to result, in physical harm or that evoke significant fear. The category is applied to the victim of the maltreatment, not the perpetrator. Also known as: Physical maltreatment | physical abuse | Shaken infant syndrome | shaken baby syndrome | Battered baby syndrome [MB23.0] Aggressive behaviour Definition: Actions intended to threaten or hurt another person or to damage property that may be physical, verbal, or symbolic (e.g., acting against the other person's interests). Aggressive behaviour may be appropriate and self-protective, or inappropriate, hostile, and destructive. Also known as: Aggressive behaviour | Violent behaviour | physical violence [QD70.Z] Problems associated with the natural environment or human-made changes to the environment, unspecified Also known as: Problems associated with the natural environment or human-made changes to the environment, unspecified | Problems associated with the natural environment or human-made changes to the environment | physical environment problem | exposure to pollution NOS | unsatisfactory physical environment [QE82.0] Personal history of physical abuse Definition: Personal history of non-accidental acts of physical force that result, or have reasonable potential to result, in physical harm or that evoke significant fear. This category is applied to the victim of the maltreatment, not the perpetrator. Also known as: Personal history of physical abuse | Personal history of physical maltreatment | Physical abuse of child Excludes: History of spouse or partner violence, physical [GA90] Hyperplasia of prostate Definition: A condition of the prostate, caused by an increased rate of cellular division of the glandular and stromal cells. This condition is characterised by enlargement of the prostatic tissue, dysuria, urinary urgency, nocturia, weak urine stream, straining while urinating, incomplete bladder emptying during urination, or increased frequency of urinary tract infection. Also known as: Hyperplasia of prostate | Adenofibromatous hypertrophy of prostate | benign prostatic hyperplasia | prostate hyperplasia | prostatic area hypertrophy Includes: Adenofibromatous hypertrophy of prostate Excludes: Benign neoplasms of prostate [GA91.Z] Inflammatory or other diseases of prostate, unspecified Also known as: Inflammatory or other diseases of prostate, unspecified | Inflammatory or other diseases of prostate | inflammation of prostate NOS | prostatitis NOS | disease of prostate NOS [GA91.Y] Other specified inflammatory or other diseases of prostate Also known as: Other specified inflammatory or other diseases of prostate | Acute bacterial prostatitis | acute prostatitis | Prostatitis category I (NIH classification) | Prostatitis category I [GA91.0] Chronic prostatitis Definition: A condition caused by obstruction of the prostate glands. This condition is characterised by inflammation of the prostate gland, dysuria, pollakiuria, urinary urgency, genital pain, lower back pain, abdominal pain, and repeated bladder infections that last for at least three months. Also known as: Chronic prostatitis | Fibrous prostatitis | Hypertrophic prostatitis | Subacute prostatitis | Chronic bacterial prostatitis === GRAPH WALKS === --- Walk 1 --- [6B03] Specific phobia Def: Specific phobia is characterised by a marked and excessive fear or anxiety that consistently occurs upon exposure or anticipation of exposure to one or more specific objects or situations (e.g., proxi... --EXCLUDES--> [?] Body dysmorphic disorder Def: Body Dysmorphic Disorder is characterised by persistent preoccupation with one or more perceived defects or flaws in appearance that are either unnoticeable or only slightly noticeable to others. Indi... --EXCLUDES--> [?] Concern about body appearance --- Walk 2 --- [6B03] Specific phobia Def: Specific phobia is characterised by a marked and excessive fear or anxiety that consistently occurs upon exposure or anticipation of exposure to one or more specific objects or situations (e.g., proxi... --EXCLUDES--> [?] Body dysmorphic disorder Def: Body Dysmorphic Disorder is characterised by persistent preoccupation with one or more perceived defects or flaws in appearance that are either unnoticeable or only slightly noticeable to others. Indi... --PARENT--> [?] Obsessive-compulsive or related disorders Def: Obsessive-compulsive and related disorders is a group of disorders characterised by repetitive thoughts and behaviours that are believed to share similarities in aetiology and key diagnostic validator... --- Walk 3 --- [MG44.1Z] Lack of expected normal physiological development, unspecified --PARENT--> [MG44.1] Lack of expected normal physiological development Def: Lack of expected normal physiological development includes delayed milestone of development and other lack of expected normal physiological development including gross and fine motor development, lang... --EXCLUDES--> [?] Delayed puberty Def: This is when an organism has passed the usual age of onset of puberty with no physical or hormonal signs that it is beginning. Puberty may be delayed for several years and still occur normally, in whi... --- Walk 4 --- [MG44.1Z] Lack of expected normal physiological development, unspecified --PARENT--> [MG44.1] Lack of expected normal physiological development Def: Lack of expected normal physiological development includes delayed milestone of development and other lack of expected normal physiological development including gross and fine motor development, lang... --EXCLUDES--> [?] Disorders of intellectual development Def: Disorders of intellectual development are a group of etiologically diverse conditions originating during the developmental period characterised by significantly below average intellectual functioning ... --- Walk 5 --- [PJ20] Physical maltreatment Def: Non-accidental acts of physical force that result, or have reasonable potential to result, in physical harm or that evoke significant fear. The category is applied to the victim of the maltreatment, n... --PARENT--> [?] Maltreatment Def: Non-accidental acts of physical force, forced or coerced sexual acts, verbal or symbolic acts, or significant caregiving omissions that result in harm or have a reasonable potential for harm. These ca... --PARENT--> [23] External causes of morbidity or mortality Def: !markdown The WHO definition of an ‘injury’ is: ‘Injuries are caused by acute exposure to physical agents such as mechanical energy, heat, electricity, chemicals, and ionizing radiation interacting wi... --- Walk 6 --- [PJ20] Physical maltreatment Def: Non-accidental acts of physical force that result, or have reasonable potential to result, in physical harm or that evoke significant fear. The category is applied to the victim of the maltreatment, n... --PARENT--> [?] Maltreatment Def: Non-accidental acts of physical force, forced or coerced sexual acts, verbal or symbolic acts, or significant caregiving omissions that result in harm or have a reasonable potential for harm. These ca... --CHILD--> [PJ21] Sexual maltreatment Def: In adults, forced or coerced sexual acts or sexual acts with someone who is unable to consent; in children, sexual acts involving a child that are intended to provide sexual gratification to an adult....
[ "[6B03] Specific phobia\n Def: Specific phobia is characterised by a marked and excessive fear or anxiety that consistently occurs upon exposure or anticipation of exposure to one or more specific objects or situations (e.g., proxi...\n --EXCLUDES--> [?] Body dysmorphic disorder\n Def: Body Dysmorphic Disorder is characterised by persistent preoccupation with one or more perceived defects or flaws in appearance that are either unnoticeable or only slightly noticeable to others. Indi...\n --EXCLUDES--> [?] Concern about body appearance", "[6B03] Specific phobia\n Def: Specific phobia is characterised by a marked and excessive fear or anxiety that consistently occurs upon exposure or anticipation of exposure to one or more specific objects or situations (e.g., proxi...\n --EXCLUDES--> [?] Body dysmorphic disorder\n Def: Body Dysmorphic Disorder is characterised by persistent preoccupation with one or more perceived defects or flaws in appearance that are either unnoticeable or only slightly noticeable to others. Indi...\n --PARENT--> [?] Obsessive-compulsive or related disorders\n Def: Obsessive-compulsive and related disorders is a group of disorders characterised by repetitive thoughts and behaviours that are believed to share similarities in aetiology and key diagnostic validator...", "[MG44.1Z] Lack of expected normal physiological development, unspecified\n --PARENT--> [MG44.1] Lack of expected normal physiological development\n Def: Lack of expected normal physiological development includes delayed milestone of development and other lack of expected normal physiological development including gross and fine motor development, lang...\n --EXCLUDES--> [?] Delayed puberty\n Def: This is when an organism has passed the usual age of onset of puberty with no physical or hormonal signs that it is beginning. Puberty may be delayed for several years and still occur normally, in whi...", "[MG44.1Z] Lack of expected normal physiological development, unspecified\n --PARENT--> [MG44.1] Lack of expected normal physiological development\n Def: Lack of expected normal physiological development includes delayed milestone of development and other lack of expected normal physiological development including gross and fine motor development, lang...\n --EXCLUDES--> [?] Disorders of intellectual development\n Def: Disorders of intellectual development are a group of etiologically diverse conditions originating during the developmental period characterised by significantly below average intellectual functioning ...", "[PJ20] Physical maltreatment\n Def: Non-accidental acts of physical force that result, or have reasonable potential to result, in physical harm or that evoke significant fear. The category is applied to the victim of the maltreatment, n...\n --PARENT--> [?] Maltreatment\n Def: Non-accidental acts of physical force, forced or coerced sexual acts, verbal or symbolic acts, or significant caregiving omissions that result in harm or have a reasonable potential for harm. These ca...\n --PARENT--> [23] External causes of morbidity or mortality\n Def: !markdown\nThe WHO definition of an ‘injury’ is: ‘Injuries are caused by acute exposure to physical agents such as mechanical energy, heat, electricity, chemicals, and ionizing radiation interacting wi...", "[PJ20] Physical maltreatment\n Def: Non-accidental acts of physical force that result, or have reasonable potential to result, in physical harm or that evoke significant fear. The category is applied to the victim of the maltreatment, n...\n --PARENT--> [?] Maltreatment\n Def: Non-accidental acts of physical force, forced or coerced sexual acts, verbal or symbolic acts, or significant caregiving omissions that result in harm or have a reasonable potential for harm. These ca...\n --CHILD--> [PJ21] Sexual maltreatment\n Def: In adults, forced or coerced sexual acts or sexual acts with someone who is unable to consent; in children, sexual acts involving a child that are intended to provide sexual gratification to an adult...." ]
6B03
Specific phobia
[ { "from_icd11": "6B03", "icd10_code": "F40240", "icd10_title": "Claustrophobia" }, { "from_icd11": "6B03", "icd10_code": "F40231", "icd10_title": "Fear of injections and transfusions" }, { "from_icd11": "6B03", "icd10_code": "F40210", "icd10_title": "Arachnophobia" }, { "from_icd11": "6B03", "icd10_code": "F40243", "icd10_title": "Fear of flying" }, { "from_icd11": "6B03", "icd10_code": "F40241", "icd10_title": "Acrophobia" }, { "from_icd11": "6B03", "icd10_code": "F40232", "icd10_title": "Fear of other medical care" }, { "from_icd11": "6B03", "icd10_code": "F40298", "icd10_title": "Other specified phobia" }, { "from_icd11": "6B03", "icd10_code": "F40218", "icd10_title": "Other animal type phobia" }, { "from_icd11": "6B03", "icd10_code": "F402", "icd10_title": "Specific (isolated) phobias" }, { "from_icd11": "MG44.1Z", "icd10_code": "R6250", "icd10_title": "Unspecified lack of expected normal physiological development in childhood" }, { "from_icd11": "MG44.1Z", "icd10_code": "R6259", "icd10_title": "Other lack of expected normal physiological development in childhood" }, { "from_icd11": "MG44.1Z", "icd10_code": "R6251", "icd10_title": "Failure to thrive (child)" }, { "from_icd11": "MG44.1Z", "icd10_code": "R6252", "icd10_title": "Short stature (child)" }, { "from_icd11": "MG44.1Z", "icd10_code": "R62", "icd10_title": "Lack of expected normal physiological development in childhood and adults" }, { "from_icd11": "MG44.1Z", "icd10_code": "R628", "icd10_title": "" } ]
F40240
Claustrophobia
In endovascular treatment of cerebrovascular diseases, the double micro-guidewire technique is used to increase catheter stability ( 18 ), facilitate stent navigation through tortuous arteries ( 19 , 20 ), and help “Y” configuration stenting in middle cerebral artery bifurcation aneurysms ( 21 ) or coil embolization of aneurysms located in the posterior circulation ( 22 ). The role of a second micro-guidewire is certainly associated with straightening of the tortuous cerebral artery to facilitate subsequent endovascular maneuver. In our case, the double micro-guidewire technique was used to rescue the collapsed stent proximal end because stent collapse may lead to serious complications of stent occlusion, thrombosis, and ischemic events. The first micro-guidewire passed through the proximal lateral stent mesh into the stent lumen, which not only straightened the tortuous vertebral artery, but also reopened the collapsed stent proximal end. It was, thus, helpful for navigation of the second micro-guidewire right through the opened stent proximal end into the stent lumen for deployment of a supporting stent to prevent collapse of the stent proximal end. When faced with a collapsed stent end in tortuous cerebral arteries, immediate action is needed to rescue the seemingly imminent severe complications of ischemic events. This case report presented an effective approach for solving this severe issue.
4.121094
0.831543
sec[2]/p[2]
en
0.999996
34539544
https://doi.org/10.3389/fneur.2021.671158
[ "stent", "micro", "guidewire", "tortuous", "cerebral", "artery", "collapsed", "endovascular", "double", "technique" ]
[ { "code": "PK93.2", "title": "Gastroenterology or urology devices associated with injury or harm, prosthetic or other implants, materials or accessory devices" }, { "code": "QB51.1", "title": "Presence of urogenital implants" }, { "code": "QB51.Y", "title": "Presence of other specified devices other than cardiac or vascular implants" }, { "code": "QB51.3", "title": "Presence of otological or audiological implants" }, { "code": "PL12.3", "title": "Obstruction of device, as mode of injury or harm" }, { "code": "LD20.1", "title": "Syndromes with lissencephaly as a major feature" }, { "code": "DA0E.00", "title": "Micrognathia" }, { "code": "LB16.Y", "title": "Other specified structural developmental anomalies of large intestine" }, { "code": "LA11.1", "title": "Structural developmental anomalies of cornea" }, { "code": "LB59", "title": "Hypoplasia of testis or scrotum" } ]
=== ICD-11 CODES FOUND === [PK93.2] Gastroenterology or urology devices associated with injury or harm, prosthetic or other implants, materials or accessory devices Also known as: Gastroenterology or urology devices associated with injury or harm, prosthetic or other implants, materials or accessory devices | Surgical operation with implant of artificial internal gastroenterology or urology device associated with abnormal reaction of the patient, or of later complication, without mention of misadventure at the time of the procedure | Surgical operation with gastroenterological or urological bypass or graft associated with abnormal reaction of the patient, or of later complication, without mention of misadventure at the time of the procedure | Gastroenterology or urology devices associated with injury or harm, urethral or ureteral stents | Incrustation or calcification of indwelling ureteral stents Excludes: Circumstances associated with a surgical or other medical device influencing the episode of care without injury or harm [QB51.1] Presence of urogenital implants Also known as: Presence of urogenital implants | Presence of bladder implant | bladder replaced by other means | replacement of bladder by artificial or mechanical device or prosthesis | Presence of urethral stent [QB51.Y] Presence of other specified devices other than cardiac or vascular implants Also known as: Presence of other specified devices other than cardiac or vascular implants | Presence of bone or tendon implants other than orthopaedic joint implants | replacement of tendon by artificial or mechanical device or prosthesis | presence of tendon implant | Presence of skull plate [QB51.3] Presence of otological or audiological implants Also known as: Presence of otological or audiological implants | presence of audiological implant | presence of hearing device implant | presence of hearing-aid implant | presence of otological implant [PL12.3] Obstruction of device, as mode of injury or harm Definition: Obstruction associated with prosthetic devices, grafts or implants Also known as: Obstruction of device, as mode of injury or harm | occlusion shunt | blockage of device causing obstruction as mode of injury | blocked tube causing obstruction as mode of injury | occlusion of device causing obstruction as mode of injury Excludes: Obstruction of device without injury or harm [LD20.1] Syndromes with lissencephaly as a major feature Definition: The term lissencephaly covers a group of rare malformations sharing the common feature of anomalies in the appearance of brain convolutions (characterised by simplification or absence of folding) associated with abnormal organisation of the cortical layers as a result of neuronal migration defects during embryogenesis. Children with lissencephaly have feeding and swallowing problems, muscle tone anomalies (early hypotonia and subsequently limb hypertonia), seizures (in particular, infantile spas Also known as: Syndromes with lissencephaly as a major feature | Pachygyria | Agyria | Classic lissencephaly | Lissencephaly type 1 Includes: Agyria | Pachygyria [DA0E.00] Micrognathia Definition: Apparently reduced length and width of the mandible when viewed from the front but not from the side. This is a bundled term comprising shortening and narrowing of the mandible and chin. Also known as: Micrognathia | Congenital micrognathia | congenital micrognathism | Acquired micrognathia Excludes: Pierre Robin syndrome [LB16.Y] Other specified structural developmental anomalies of large intestine Also known as: Other specified structural developmental anomalies of large intestine | Intestinal neuronal dysplasia | Congenital diverticulum of large intestine | congenital colon diverticulum | Duplication of large intestine [LA11.1] Structural developmental anomalies of cornea Definition: Any condition caused by failure of the cornea to correctly develop during the antenatal period. Also known as: Structural developmental anomalies of cornea | Malformations of cornea | Cornea plana | Flat cornea | Cornea plana, unilateral [LB59] Hypoplasia of testis or scrotum Definition: A condition caused by incomplete development of the testis and scrotum during the antenatal period. This condition is characterised by a decrease or destruction in the number or size of cells testis and scrotal tissue. Also known as: Hypoplasia of testis or scrotum | Congenital hypoplasia of testis | testicular hypoplasia | congenital small testis | hypoplasia of testes === GRAPH WALKS === --- Walk 1 --- [PK93.2] Gastroenterology or urology devices associated with injury or harm, prosthetic or other implants, materials or accessory devices --EXCLUDES--> [?] Circumstances associated with a surgical or other medical device influencing the episode of care without injury or harm --CHILD--> [?] Structural device failure without injury or harm Def: Mechanical or material device failure not related to the installation of the device without any documented injury or harm.... --- Walk 2 --- [PK93.2] Gastroenterology or urology devices associated with injury or harm, prosthetic or other implants, materials or accessory devices --EXCLUDES--> [?] Circumstances associated with a surgical or other medical device influencing the episode of care without injury or harm --CHILD--> [?] Functional device failure without injury or harm Def: A device not working or operating correctly, or that has stopped functioning after a period of function, but without documented injury or harm to the patient.... --- Walk 3 --- [QB51.1] Presence of urogenital implants --PARENT--> [QB51] Presence of devices other than cardiac or vascular implants --CHILD--> [QB51.1] Presence of urogenital implants --- Walk 4 --- [QB51.1] Presence of urogenital implants --PARENT--> [QB51] Presence of devices other than cardiac or vascular implants --PARENT--> [?] Presence of device, implants or grafts --- Walk 5 --- [QB51.Y] Presence of other specified devices other than cardiac or vascular implants --PARENT--> [QB51] Presence of devices other than cardiac or vascular implants --EXCLUDES--> [?] Fitting, adjustment or management of devices --- Walk 6 --- [QB51.Y] Presence of other specified devices other than cardiac or vascular implants --PARENT--> [QB51] Presence of devices other than cardiac or vascular implants --PARENT--> [?] Presence of device, implants or grafts
[ "[PK93.2] Gastroenterology or urology devices associated with injury or harm, prosthetic or other implants, materials or accessory devices\n --EXCLUDES--> [?] Circumstances associated with a surgical or other medical device influencing the episode of care without injury or harm\n --CHILD--> [?] Structural device failure without injury or harm\n Def: Mechanical or material device failure not related to the installation of the device without any documented injury or harm....", "[PK93.2] Gastroenterology or urology devices associated with injury or harm, prosthetic or other implants, materials or accessory devices\n --EXCLUDES--> [?] Circumstances associated with a surgical or other medical device influencing the episode of care without injury or harm\n --CHILD--> [?] Functional device failure without injury or harm\n Def: A device not working or operating correctly, or that has stopped functioning after a period of function, but without documented injury or harm to the patient....", "[QB51.1] Presence of urogenital implants\n --PARENT--> [QB51] Presence of devices other than cardiac or vascular implants\n --CHILD--> [QB51.1] Presence of urogenital implants", "[QB51.1] Presence of urogenital implants\n --PARENT--> [QB51] Presence of devices other than cardiac or vascular implants\n --PARENT--> [?] Presence of device, implants or grafts", "[QB51.Y] Presence of other specified devices other than cardiac or vascular implants\n --PARENT--> [QB51] Presence of devices other than cardiac or vascular implants\n --EXCLUDES--> [?] Fitting, adjustment or management of devices", "[QB51.Y] Presence of other specified devices other than cardiac or vascular implants\n --PARENT--> [QB51] Presence of devices other than cardiac or vascular implants\n --PARENT--> [?] Presence of device, implants or grafts" ]
PK93.2
Gastroenterology or urology devices associated with injury or harm, prosthetic or other implants, materials or accessory devices
[ { "from_icd11": "PK93.2", "icd10_code": "T83711A", "icd10_title": "Erosion of implanted vaginal mesh to surrounding organ or tissue, initial encounter" }, { "from_icd11": "PK93.2", "icd10_code": "T83718A", "icd10_title": "Erosion of other implanted mesh to organ or tissue, initial encounter" }, { "from_icd11": "PK93.2", "icd10_code": "T83728A", "icd10_title": "Exposure of other implanted mesh into organ or tissue, initial encounter" }, { "from_icd11": "PK93.2", "icd10_code": "T83719A", "icd10_title": "Erosion of other prosthetic materials to surrounding organ or tissue, initial encounter" }, { "from_icd11": "PK93.2", "icd10_code": "T83718S", "icd10_title": "Erosion of other implanted mesh to organ or tissue, sequela" }, { "from_icd11": "PK93.2", "icd10_code": "T83712A", "icd10_title": "Erosion of implanted urethral mesh to surrounding organ or tissue, initial encounter" }, { "from_icd11": "PK93.2", "icd10_code": "T83721A", "icd10_title": "Exposure of implanted vaginal mesh into vagina, initial encounter" }, { "from_icd11": "PK93.2", "icd10_code": "T85590A", "icd10_title": "Other mechanical complication of bile duct prosthesis, initial encounter" }, { "from_icd11": "PK93.2", "icd10_code": "T83490A", "icd10_title": "Other mechanical complication of implanted penile prosthesis, initial encounter" }, { "from_icd11": "PK93.2", "icd10_code": "T85598A", "icd10_title": "Other mechanical complication of other gastrointestinal prosthetic devices, implants and grafts, initial encounter" }, { "from_icd11": "PK93.2", "icd10_code": "T85528A", "icd10_title": "Displacement of other gastrointestinal prosthetic devices, implants and grafts, initial encounter" }, { "from_icd11": "PK93.2", "icd10_code": "T85520A", "icd10_title": "Displacement of bile duct prosthesis, initial encounter" }, { "from_icd11": "PK93.2", "icd10_code": "T83193A", "icd10_title": "Other mechanical complication of other urinary stent, initial encounter" }, { "from_icd11": "PK93.2", "icd10_code": "T83123A", "icd10_title": "Displacement of other urinary stents, initial encounter" }, { "from_icd11": "PK93.2", "icd10_code": "T83111A", "icd10_title": "Breakdown (mechanical) of implanted urinary sphincter, initial encounter" } ]
T83711A
Erosion of implanted vaginal mesh to surrounding organ or tissue, initial encounter
We paid close attention to the neurological symptoms with regard to long-lasting severe anemia and hypoxemia both in utero and after delivery. The baby showed no clinically abnormal neurological symptoms during hospitalization. Cranial ultrasound on days 1, 2, 4 and 11 after birth revealed an increased resistance index (RI) of the middle cerebral artery but no hypoxic or ischemic changes (edema, hemorrhage, etc.) and no signs of periventricular leukomalacia (PVL). Moreover, the amplitude integrated electroencephalogram (aEEG) on the second day after birth showed that a sleep cycle appeared, a discontinuous quiet sleep period, and no seizures under video monitoring, which were all normal for a preterm infant at 31 + 5 weeks gestation. Assessment of general movements (GMs) (performed 13 days after birth) showed normal movement of the body. Both ears passed the automatic auditory brainstem response (AABR) test in the hearing screen. At 34 + 5 weeks of corrected gestation before discharge, brain magnetic resonance imaging (MRI) presented a normal structure according to gestation, and no signs of PVL or other abnormalities were noted. After 24 days of hospitalization (34 + 6 gestation), the baby was discharged with a body weight of 1810 g, body length of 40.4 cm, and head circumference of 28.5 cm. All of these values were less than the 10th percentiles, implying extrauterine growth restriction (EUGR).
4.074219
0.958496
sec[1]/sec[1]/sec[2]/p[0]
en
0.999997
34663239
https://doi.org/10.1186/s12884-021-04179-5
[ "gestation", "birth", "body", "neurological", "both", "baby", "hospitalization", "sleep", "paid", "close" ]
[ { "code": "JA61.Y", "title": "Other specified venous complications in pregnancy" }, { "code": "JA8E", "title": "Maternal care related to prolonged pregnancy" }, { "code": "JA01.Y", "title": "Other specified ectopic pregnancy" }, { "code": "JA61.Z", "title": "Venous complications in pregnancy, unspecified" }, { "code": "JA82.5", "title": "Maternal care for multiple gestation with malpresentation of one fetus or more" }, { "code": "QA46.Z", "title": "Outcome of delivery, unspecified" }, { "code": "LD9Z", "title": "Developmental anomalies, unspecified" }, { "code": "LD2Z", "title": "Multiple developmental anomalies or syndromes, unspecified" }, { "code": "KA4Z", "title": "Birth injury, unspecified" }, { "code": "QA46.0", "title": "Single live birth" } ]
=== ICD-11 CODES FOUND === [JA61.Y] Other specified venous complications in pregnancy Also known as: Other specified venous complications in pregnancy | Venous thrombosis in pregnancy | antepartum thrombosis NOS | Gestational thrombosis NOS | thrombosis in pregnancy NOS [JA8E] Maternal care related to prolonged pregnancy Definition: Pregnancy that has exceeded a duration of 42 weeks from the last menstrual period. Also known as: Maternal care related to prolonged pregnancy | post-term pregnancy | pregnancy beyond 42 weeks of gestation | prolonged gestation | postmature pregnancy Includes: Post-term [JA01.Y] Other specified ectopic pregnancy Also known as: Other specified ectopic pregnancy | Cornual gestation or pregnancy | cornual gestation | cornual pregnancy | Cervical pregnancy [JA61.Z] Venous complications in pregnancy, unspecified Also known as: Venous complications in pregnancy, unspecified | Venous complications in pregnancy | Gestational phlebopathy, NOS [JA82.5] Maternal care for multiple gestation with malpresentation of one fetus or more Also known as: Maternal care for multiple gestation with malpresentation of one fetus or more | abnormal presentation in multiple gestation [QA46.Z] Outcome of delivery, unspecified Also known as: Outcome of delivery, unspecified | Outcome of delivery | Multiple birth, unspecified | Single birth, unspecified [LD9Z] Developmental anomalies, unspecified Also known as: Developmental anomalies, unspecified | congenital malformations, deformations and chromosomal abnormalities | congenital malformation NOS | developmental abnormality NOS | fetal abnormality NOS [LD2Z] Multiple developmental anomalies or syndromes, unspecified Also known as: Multiple developmental anomalies or syndromes, unspecified | multiple congenital birth defects NOS | multiple congenital birth deformities NOS | multiple fetal abnormalities NOS | severe birth deformities NOS [KA4Z] Birth injury, unspecified Also known as: Birth injury, unspecified | childbirth trauma | birth injury nos | birth trauma of fetus | childbirth injury [QA46.0] Single live birth Definition: Live birth is the complete expulsion or extraction from a woman of a fetus, irrespective of the duration of the pregnancy, which, after such separation, shows signs of life. Also known as: Single live birth | single liveborn | outcome of delivery of single liveborn === GRAPH WALKS === --- Walk 1 --- [JA61.Y] Other specified venous complications in pregnancy --PARENT--> [JA61] Venous complications in pregnancy --EXCLUDES--> [?] Obstetric blood-clot embolism Def: A condition characterised by the lodging of a blood clot (a specific type of embolus known as a thrombus) in the bloodstream, which can cause a blockage associated with the physiological and other cha... --- Walk 2 --- [JA61.Y] Other specified venous complications in pregnancy --PARENT--> [JA61] Venous complications in pregnancy --EXCLUDES--> [?] Venous complications in the puerperium --- Walk 3 --- [JA8E] Maternal care related to prolonged pregnancy Def: Pregnancy that has exceeded a duration of 42 weeks from the last menstrual period.... --PARENT--> [?] Maternal care related to the fetus, amniotic cavity or possible delivery problems Def: A group of conditions characterised by the provision of health interventions to the mother due to conditions associated with the fetus, the amniotic cavity, or to issues associated with labour and del... --CHILD--> [JA80] Maternal care related to multiple gestation --- Walk 4 --- [JA8E] Maternal care related to prolonged pregnancy Def: Pregnancy that has exceeded a duration of 42 weeks from the last menstrual period.... --PARENT--> [?] Maternal care related to the fetus, amniotic cavity or possible delivery problems Def: A group of conditions characterised by the provision of health interventions to the mother due to conditions associated with the fetus, the amniotic cavity, or to issues associated with labour and del... --CHILD--> [JA81] Maternal care related to complications specific to multiple gestation --- Walk 5 --- [JA01.Y] Other specified ectopic pregnancy --PARENT--> [JA01] Ectopic pregnancy Def: Any condition characterised by implantation of the embryo outside the endometrium and endometrial cavity during pregnancy.... --PARENT--> [?] Abortive outcome of pregnancy Def: A group of conditions characterised by pregnancy which does not result in live offspring. These conditions include e.g. abortion, ectopic pregnancy or molar pregnancy.... --- Walk 6 --- [JA01.Y] Other specified ectopic pregnancy --PARENT--> [JA01] Ectopic pregnancy Def: Any condition characterised by implantation of the embryo outside the endometrium and endometrial cavity during pregnancy.... --CHILD--> [JA01.2] Ovarian pregnancy Def: A condition characterised by implantation of the embryo within the ovary during pregnancy....
[ "[JA61.Y] Other specified venous complications in pregnancy\n --PARENT--> [JA61] Venous complications in pregnancy\n --EXCLUDES--> [?] Obstetric blood-clot embolism\n Def: A condition characterised by the lodging of a blood clot (a specific type of embolus known as a thrombus) in the bloodstream, which can cause a blockage associated with the physiological and other cha...", "[JA61.Y] Other specified venous complications in pregnancy\n --PARENT--> [JA61] Venous complications in pregnancy\n --EXCLUDES--> [?] Venous complications in the puerperium", "[JA8E] Maternal care related to prolonged pregnancy\n Def: Pregnancy that has exceeded a duration of 42 weeks from the last menstrual period....\n --PARENT--> [?] Maternal care related to the fetus, amniotic cavity or possible delivery problems\n Def: A group of conditions characterised by the provision of health interventions to the mother due to conditions associated with the fetus, the amniotic cavity, or to issues associated with labour and del...\n --CHILD--> [JA80] Maternal care related to multiple gestation", "[JA8E] Maternal care related to prolonged pregnancy\n Def: Pregnancy that has exceeded a duration of 42 weeks from the last menstrual period....\n --PARENT--> [?] Maternal care related to the fetus, amniotic cavity or possible delivery problems\n Def: A group of conditions characterised by the provision of health interventions to the mother due to conditions associated with the fetus, the amniotic cavity, or to issues associated with labour and del...\n --CHILD--> [JA81] Maternal care related to complications specific to multiple gestation", "[JA01.Y] Other specified ectopic pregnancy\n --PARENT--> [JA01] Ectopic pregnancy\n Def: Any condition characterised by implantation of the embryo outside the endometrium and endometrial cavity during pregnancy....\n --PARENT--> [?] Abortive outcome of pregnancy\n Def: A group of conditions characterised by pregnancy which does not result in live offspring. These conditions include e.g. abortion, ectopic pregnancy or molar pregnancy....", "[JA01.Y] Other specified ectopic pregnancy\n --PARENT--> [JA01] Ectopic pregnancy\n Def: Any condition characterised by implantation of the embryo outside the endometrium and endometrial cavity during pregnancy....\n --CHILD--> [JA01.2] Ovarian pregnancy\n Def: A condition characterised by implantation of the embryo within the ovary during pregnancy...." ]
JA61.Y
Other specified venous complications in pregnancy
[ { "from_icd11": "JA8E", "icd10_code": "O480", "icd10_title": "Post-term pregnancy" }, { "from_icd11": "JA8E", "icd10_code": "O481", "icd10_title": "Prolonged pregnancy" }, { "from_icd11": "JA8E", "icd10_code": "O48", "icd10_title": "Late pregnancy" }, { "from_icd11": "JA8E", "icd10_code": "O480 ", "icd10_title": "" }, { "from_icd11": "JA61.Z", "icd10_code": "O2293", "icd10_title": "Venous complication in pregnancy, unspecified, third trimester" }, { "from_icd11": "JA61.Z", "icd10_code": "O228X3", "icd10_title": "Other venous complications in pregnancy, third trimester" }, { "from_icd11": "JA61.Z", "icd10_code": "O228X1", "icd10_title": "Other venous complications in pregnancy, first trimester" }, { "from_icd11": "JA61.Z", "icd10_code": "O228X2", "icd10_title": "Other venous complications in pregnancy, second trimester" }, { "from_icd11": "JA61.Z", "icd10_code": "O2291", "icd10_title": "Venous complication in pregnancy, unspecified, first trimester" }, { "from_icd11": "JA61.Z", "icd10_code": "O2292", "icd10_title": "Venous complication in pregnancy, unspecified, second trimester" }, { "from_icd11": "JA61.Z", "icd10_code": "O22", "icd10_title": "Venous complications and hemorrhoids in pregnancy" }, { "from_icd11": "JA61.Z", "icd10_code": "O228", "icd10_title": "Other venous complications in pregnancy" }, { "from_icd11": "JA61.Z", "icd10_code": "O229", "icd10_title": "Venous complication in pregnancy, unspecified" }, { "from_icd11": "JA82.5", "icd10_code": "O325", "icd10_title": "" }, { "from_icd11": "QA46.Z", "icd10_code": "Z379", "icd10_title": "Outcome of delivery, unspecified" } ]
O480
Post-term pregnancy
Enteral feedings have demonstrated superior patient outcomes compared to parenteral nutrition, decreasing costs and reducing hospital-acquired infections . First explained in 1980, percutaneous endoscopic gastrostomy (PEG) has become a commonly utilized technique for enteral nutrition support . While considered a generally safe procedure, complications, including skin maceration, leakage, and infection, have been reported to varying degrees . More severe injuries, including intraabdominal bleeding and injury to surrounding organ structures, are concerns that must be mitigated by the performing physician . Positioning the transverse colon over the anterior gastric wall could lead to colonic injury during PEG placement . As per protocol in most hospitals, a pre-procedure CT scan of the abdomen is usually done to evaluate the position of the transverse colon. Sometimes, laparoscopic assistance is done to assist in the safe placement of the PEG tube. Gastrocolocutaneous fistula is an epithelial connection between the stomach mucosa, colon, and abdominal skin. Potential etiologies include penetration of the colon during PEG insertion from the skin into the stomach through accidental puncture or gradual erosion of the tube into the adjacent bowel . Here, we report on a novel approach to the management of a patient who developed a gastrocolocutaneous fistula from PEG insertion at an outside institution.
4.148438
0.760254
sec[0]/p[0]
en
0.999994
39105023
https://doi.org/10.7759/cureus.63908
[ "colon", "skin", "enteral", "nutrition", "safe", "including", "injury", "transverse", "placement", "tube" ]
[ { "code": "1A40.0&XA03U9", "title": "Colon inflammation" }, { "code": "DB30.Y&XA03U9", "title": "Obstructed colon" }, { "code": "NB91.81", "title": "Laceration of colon" }, { "code": "DD3Z", "title": "Ischaemic vascular disorders of intestine, unspecified" }, { "code": "DB32.2Z&XA03U9", "title": "Colonic dilatation" }, { "code": "ME67", "title": "Skin disorder of uncertain or unspecified nature" }, { "code": "ME66.Y", "title": "Other specified skin changes" }, { "code": "EM0Y", "title": "Other specified diseases of the skin" }, { "code": "ME60.Z", "title": "Skin lesion of unspecified nature" }, { "code": "ME66.1", "title": "Changes in skin texture" } ]
=== ICD-11 CODES FOUND === [NB91.81] Laceration of colon Definition: A tear or wound of large intestine. Also known as: Laceration of colon [DD3Z] Ischaemic vascular disorders of intestine, unspecified Also known as: Ischaemic vascular disorders of intestine, unspecified | Vascular disorder of intestine, not elsewhere classified | vascular disorder of intestine | vascular bowel disease | ischaemic gut NOS [ME67] Skin disorder of uncertain or unspecified nature Definition: A category to enable the presence of a skin disorder to be recorded without making assumptions as to the precise nature of the disorder in question. Also known as: Skin disorder of uncertain or unspecified nature | Skin disorder without established diagnosis | change of skin NOS | dermatological disease NOS | dermatological disorder NOS [ME66.Y] Other specified skin changes Also known as: Other specified skin changes | Cutis marmorata | Fear of skin disease | Retention hyperkeratosis | Dermatitis neglecta [EM0Y] Other specified diseases of the skin Also known as: Other specified diseases of the skin | Adverse cutaneous effects of healthcare related interventions | Cutaneous complications of surgical, laser or other interventional procedures | Postprocedural cutaneous complications of surgical, laser or other interventions | Cutaneous complications of surgical procedures [ME60.Z] Skin lesion of unspecified nature Also known as: Skin lesion of unspecified nature | Skin lesion of uncertain or unspecified nature | Skin lesion without established diagnosis | Pigmented skin lesion of unspecified nature | Ulcer of skin of unspecified nature [ME66.1] Changes in skin texture Definition: Alterations in skin texture of unspecified cause. Also known as: Changes in skin texture | Skin textural disturbance | Thickening of skin | induration of skin | Skin sclerosis === GRAPH WALKS === --- Walk 1 --- [NB91.81] Laceration of colon Def: A tear or wound of large intestine.... --PARENT--> [NB91.8] Injury of colon --CHILD--> [NB91.80] Contusion of colon Def: An injury to large intestine resulting from a blow in which the subsurface tissue is injured and often internally bled but the skin is not broken.... --- Walk 2 --- [NB91.81] Laceration of colon Def: A tear or wound of large intestine.... --PARENT--> [NB91.8] Injury of colon --CHILD--> [NB91.82] Primary blast injury of colon Def: An injury to large intestine resulting from direct or indirect exposure to explosion. Primary injuries are caused by high-order explosives or shock waves.... --- Walk 3 --- [DD3Z] Ischaemic vascular disorders of intestine, unspecified --PARENT--> [?] Ischaemic vascular disorders of intestine Def: Intestinal ischemia characterised by blood supply to the gastrointestinal tract that is inadequate to meet its metabolic demand... --CHILD--> [DD31] Chronic vascular disorders of intestine --- Walk 4 --- [DD3Z] Ischaemic vascular disorders of intestine, unspecified --PARENT--> [?] Ischaemic vascular disorders of intestine Def: Intestinal ischemia characterised by blood supply to the gastrointestinal tract that is inadequate to meet its metabolic demand... --RELATED_TO--> [?] Angiodysplasia of colon Def: Small dilated submucosal vessels of colonic mucosa with perforating vessels going through the muscularis mucosae....
[ "[NB91.81] Laceration of colon\n Def: A tear or wound of large intestine....\n --PARENT--> [NB91.8] Injury of colon\n --CHILD--> [NB91.80] Contusion of colon\n Def: An injury to large intestine resulting from a blow in which the subsurface tissue is injured and often internally bled but the skin is not broken....", "[NB91.81] Laceration of colon\n Def: A tear or wound of large intestine....\n --PARENT--> [NB91.8] Injury of colon\n --CHILD--> [NB91.82] Primary blast injury of colon\n Def: An injury to large intestine resulting from direct or indirect exposure to explosion. Primary injuries are caused by high-order explosives or shock waves....", "[DD3Z] Ischaemic vascular disorders of intestine, unspecified\n --PARENT--> [?] Ischaemic vascular disorders of intestine\n Def: Intestinal ischemia characterised by blood supply to the gastrointestinal tract that is inadequate to meet its metabolic demand...\n --CHILD--> [DD31] Chronic vascular disorders of intestine", "[DD3Z] Ischaemic vascular disorders of intestine, unspecified\n --PARENT--> [?] Ischaemic vascular disorders of intestine\n Def: Intestinal ischemia characterised by blood supply to the gastrointestinal tract that is inadequate to meet its metabolic demand...\n --RELATED_TO--> [?] Angiodysplasia of colon\n Def: Small dilated submucosal vessels of colonic mucosa with perforating vessels going through the muscularis mucosae...." ]
1A40.0&XA03U9
Colon inflammation
[ { "from_icd11": "DD3Z", "icd10_code": "K559", "icd10_title": "Vascular disorder of intestine, unspecified" }, { "from_icd11": "DD3Z", "icd10_code": "K558", "icd10_title": "Other vascular disorders of intestine" }, { "from_icd11": "DD3Z", "icd10_code": "K55-K64", "icd10_title": "" }, { "from_icd11": "DD3Z", "icd10_code": "K55", "icd10_title": "Vascular disorders of intestine" }, { "from_icd11": "ME67", "icd10_code": "L989", "icd10_title": "Disorder of the skin and subcutaneous tissue, unspecified" }, { "from_icd11": "ME66.Y", "icd10_code": "L578", "icd10_title": "Other skin changes due to chronic exposure to nonionizing radiation" }, { "from_icd11": "EM0Y", "icd10_code": "L918", "icd10_title": "Other hypertrophic disorders of the skin" }, { "from_icd11": "EM0Y", "icd10_code": "L988", "icd10_title": "Other specified disorders of the skin and subcutaneous tissue" }, { "from_icd11": "ME66.1", "icd10_code": "R234", "icd10_title": "Changes in skin texture" } ]
K559
Vascular disorder of intestine, unspecified
The ECMO treatment used in this patient has the following advantages: 1) generally, systemic anticoagulation is required during ECMO diversion, which may increase the risk of bleeding during surgery. In this case, ECMO pipelines were established after thyroid tumor resection. The ECMO turnaround time was very short during tracheal resection and anastomosis. Protamine injection was used to neutralize heparin immediately after the removal of ECMO, so there would be no large blood loss during the operation. 2) There are many intubation modes that can be selected during ECMO operation, such as femoral arteriovenous intubation, internal jugular vein intubation, and common carotid artery intubation, which provide multiple anesthesia modes. 3) V-V ECMO is used to maintain a satisfactory oxygen supply without endotracheal intubation. 4) ECMO reduces the impact of tracheal intubation on the surgical field in a narrow space, improves the accuracy of anastomosis, and clearly avoids injury to the recurrent laryngeal nerve during anastomosis. There are also disadvantages in this case: ECMO does increase the cost of treatment, and the operation time will increase accordingly. However, we believe that under the condition of ECMO, the visual field of end-to-end tracheal anastomosis is more sufficient, and the anastomosis time can be greatly shortened, which actually shortens the operation time in another aspect.
4.046875
0.657715
sec[2]/sec[3]/p[2]
en
0.999995
PMC9878384
https://doi.org/10.3389/fonc.2022.990600
[ "ecmo", "intubation", "anastomosis", "time", "used", "this", "which", "increase", "tracheal", "resection" ]
[ { "code": "PK81.1", "title": "Extracorporeal life support procedure associated with injury or harm in therapeutic use" }, { "code": "QC48.Y", "title": "Other specified personal history of medical treatment" }, { "code": "NE87", "title": "Failed or difficult intubation" }, { "code": "JA67.50", "title": "Failed intubation during pregnancy" }, { "code": "JB43.50", "title": "Failed intubation during the puerperium" }, { "code": "JA67.51", "title": "Difficult intubation during pregnancy" }, { "code": "JB43.51", "title": "Difficult intubation during the puerperium" }, { "code": "NE81.3", "title": "Postsurgical leak" }, { "code": "QB6Y", "title": "Other specified surgical or postsurgical states" }, { "code": "GC01.0", "title": "Bladder neck obstruction" } ]
=== ICD-11 CODES FOUND === [PK81.1] Extracorporeal life support procedure associated with injury or harm in therapeutic use Also known as: Extracorporeal life support procedure associated with injury or harm in therapeutic use | ECMO - [extracorporeal membrane oxygenation] | complication during or following extracorporeal life support procedure Excludes: Circumstances associated with a surgical or other medical procedure influencing the episode of care, without injury or harm [QC48.Y] Other specified personal history of medical treatment Also known as: Other specified personal history of medical treatment | Personal history of contraception | history of contraception | Personal history of long-term use of medicaments other than anticoagulants | personal history of long term current use of medicaments [NE87] Failed or difficult intubation Definition: Intubation complicated by patient anatomy or physiology which complicates, prolongs or prevents intubation. Complication is defined as saturations falling more than 20% below baseline, significant damage to lips, teeth or tongue, or regurgitation and aspiration of gastric contents. Prolongation is defined as either intubation using special techniques (fibreoptic intubation) or three or more attempts at intubation using direct laryngoscopy or videolaryngoscopy when performed by a fully trained a Also known as: Failed or difficult intubation | Failed intubation | Difficult intubation Excludes: Failed or difficult intubation during pregnancy | Failed or difficult intubation during labour or delivery | Failed or difficult intubation during the puerperium [JA67.50] Failed intubation during pregnancy Also known as: Failed intubation during pregnancy [JB43.50] Failed intubation during the puerperium Also known as: Failed intubation during the puerperium [JA67.51] Difficult intubation during pregnancy Also known as: Difficult intubation during pregnancy [JB43.51] Difficult intubation during the puerperium Also known as: Difficult intubation during the puerperium [NE81.3] Postsurgical leak Also known as: Postsurgical leak | postoperative leak | Postsurgical air leak | postoperative air leak | Postsurgical bile leak Excludes: Malfunction or complication of external stoma of digestive organs | Tracheostomy malfunction [QB6Y] Other specified surgical or postsurgical states Also known as: Other specified surgical or postsurgical states | Presence of intestinal bypass or anastomosis | intestinal bypass and anastomosis status | anastomosis status | intestinal bypass status [GC01.0] Bladder neck obstruction Definition: A condition of the bladder, caused by congenital or acquired abnormalities that impair the muscles that connect the bladder to the urethra. This condition is characterised by obstruction of the bladder neck and constricted opening during urination. This condition may also present with pelvic pain, pollakiuria, incontinence, or incomplete bladder emptying. Confirmation is by video urodynamics to observe the obstruction as the bladder fills and voids. Also known as: Bladder neck obstruction | bladder outlet obstruction | obstruction of bladder neck or vesicourethral orifice | vesicourethral orifice obstruction | BNO - [bladder neck obstruction] Includes: Acquired bladder neck stenosis === GRAPH WALKS === --- Walk 1 --- [PK81.1] Extracorporeal life support procedure associated with injury or harm in therapeutic use --EXCLUDES--> [?] Circumstances associated with a surgical or other medical procedure influencing the episode of care, without injury or harm --EXCLUDES--> [?] Mode of injury or harm associated with a surgical or other medical procedure --- Walk 2 --- [PK81.1] Extracorporeal life support procedure associated with injury or harm in therapeutic use --PARENT--> [PK81] Certain medical procedures associated with injury or harm in therapeutic use --RELATED_TO--> [?] Skin complications of BCG immunisation Def: Complications secondary to immunization with attenuated Mycobacterium bovis (Bacillus Calmette-Guérin or BCG).... --- Walk 3 --- [QC48.Y] Other specified personal history of medical treatment --PARENT--> [QC48] Personal history of medical treatment --CHILD--> [QC48.Y] Other specified personal history of medical treatment --- Walk 4 --- [QC48.Y] Other specified personal history of medical treatment --PARENT--> [QC48] Personal history of medical treatment --CHILD--> [QC48.Z] Personal history of medical treatment, unspecified --- Walk 5 --- [NE87] Failed or difficult intubation Def: Intubation complicated by patient anatomy or physiology which complicates, prolongs or prevents intubation. Complication is defined as saturations falling more than 20% below baseline, significant da... --EXCLUDES--> [?] Failed or difficult intubation during labour or delivery --CHILD--> [?] Failed intubation during labour or delivery --- Walk 6 --- [NE87] Failed or difficult intubation Def: Intubation complicated by patient anatomy or physiology which complicates, prolongs or prevents intubation. Complication is defined as saturations falling more than 20% below baseline, significant da... --EXCLUDES--> [?] Failed or difficult intubation during labour or delivery --CHILD--> [?] Failed intubation during labour or delivery
[ "[PK81.1] Extracorporeal life support procedure associated with injury or harm in therapeutic use\n --EXCLUDES--> [?] Circumstances associated with a surgical or other medical procedure influencing the episode of care, without injury or harm\n --EXCLUDES--> [?] Mode of injury or harm associated with a surgical or other medical procedure", "[PK81.1] Extracorporeal life support procedure associated with injury or harm in therapeutic use\n --PARENT--> [PK81] Certain medical procedures associated with injury or harm in therapeutic use\n --RELATED_TO--> [?] Skin complications of BCG immunisation\n Def: Complications secondary to immunization with attenuated Mycobacterium bovis (Bacillus Calmette-Guérin or BCG)....", "[QC48.Y] Other specified personal history of medical treatment\n --PARENT--> [QC48] Personal history of medical treatment\n --CHILD--> [QC48.Y] Other specified personal history of medical treatment", "[QC48.Y] Other specified personal history of medical treatment\n --PARENT--> [QC48] Personal history of medical treatment\n --CHILD--> [QC48.Z] Personal history of medical treatment, unspecified", "[NE87] Failed or difficult intubation\n Def: Intubation complicated by patient anatomy or physiology which complicates, prolongs or prevents intubation.\n\nComplication is defined as saturations falling more than 20% below baseline, significant da...\n --EXCLUDES--> [?] Failed or difficult intubation during labour or delivery\n --CHILD--> [?] Failed intubation during labour or delivery", "[NE87] Failed or difficult intubation\n Def: Intubation complicated by patient anatomy or physiology which complicates, prolongs or prevents intubation.\n\nComplication is defined as saturations falling more than 20% below baseline, significant da...\n --EXCLUDES--> [?] Failed or difficult intubation during labour or delivery\n --CHILD--> [?] Failed intubation during labour or delivery" ]
PK81.1
Extracorporeal life support procedure associated with injury or harm in therapeutic use
[ { "from_icd11": "QC48.Y", "icd10_code": "Z794", "icd10_title": "Long term (current) use of insulin" }, { "from_icd11": "QC48.Y", "icd10_code": "Z7902", "icd10_title": "Long term (current) use of antithrombotics/antiplatelets" }, { "from_icd11": "QC48.Y", "icd10_code": "Z7982", "icd10_title": "Long term (current) use of aspirin" }, { "from_icd11": "QC48.Y", "icd10_code": "Z7984", "icd10_title": "Long term (current) use of oral hypoglycemic drugs" }, { "from_icd11": "QC48.Y", "icd10_code": "Z79899", "icd10_title": "Other long term (current) drug therapy" }, { "from_icd11": "NE87", "icd10_code": "T884XXA", "icd10_title": "Failed or difficult intubation, initial encounter" }, { "from_icd11": "NE87", "icd10_code": "T884XXS", "icd10_title": "Failed or difficult intubation, sequela" }, { "from_icd11": "NE87", "icd10_code": "T884XXD", "icd10_title": "Failed or difficult intubation, subsequent encounter" }, { "from_icd11": "NE87", "icd10_code": "T884", "icd10_title": "Failed or difficult intubation" }, { "from_icd11": "QB6Y", "icd10_code": "Z98890", "icd10_title": "Other specified postprocedural states" }, { "from_icd11": "GC01.0", "icd10_code": "N320", "icd10_title": "Bladder-neck obstruction" } ]
Z794
Long term (current) use of insulin
Due to his uncontrolled diabetes, his visual acuity at baseline on presentation was light perception in the right eye and no light perception in the left eye. Upon GW admission, his visual acuity was bare LP OD and NLP OS. Initial blood cultures at the outside hospital were positive for Methicillin-resistant staph aureus (MRSA) but five subsequent blood cultures performed during the subsequent hospital admission to GW were negative. On initial examination, there was significant proptosis and periorbital edema as well as erythema and tenderness of the left eye. There was 360 degrees of chemosis, and the cornea showed early signs of band keratopathy and stromal edema. Anterior chamber and lens were difficult to evaluate due to the high degree of corneal decompensation. The right eye had less extensive erythema and tenderness without proptosis. There was no chemosis, and the cornea showed early band keratopathy with keratic precipitates on the endothelium. The anterior chamber was difficult to evaluate for cell. Iris was responsive to light although sluggish. Lens was clear. A B-scan was performed in both eyes. In the right eye, it showed a tractional retinal detachment involving the macula. In the left eye, B scan demonstrated a tented globe and a total funnel retinal detachment along with hyperechoic opacities in the vitreous which could represent vitreous cells, a fibrous membrane, or hemorrhage.
3.890625
0.982422
sec[1]/p[1]
en
0.999998
37069286
https://doi.org/10.1186/s12348-023-00344-3
[ "light", "visual", "acuity", "perception", "blood", "cultures", "proptosis", "edema", "erythema", "tenderness" ]
[ { "code": "KA21.2Z", "title": "Low birth weight of newborn, unspecified" }, { "code": "MB48.3", "title": "Light-headedness" }, { "code": "9D45", "title": "Impairment of light sensitivity" }, { "code": "GA20.51", "title": "Light menstrual bleeding" }, { "code": "2A83.52", "title": "Light chain deposition disease" }, { "code": "9E1Z", "title": "Diseases of the visual system, unspecified" }, { "code": "MC1Y", "title": "Other specified symptoms or signs involving the visual system" }, { "code": "9D9Z", "title": "Vision impairment, unspecified" }, { "code": "9D90.2", "title": "Moderate vision impairment" }, { "code": "QA00.6Z", "title": "Examination of eyes or vision, unspecified" } ]
=== ICD-11 CODES FOUND === [KA21.2Z] Low birth weight of newborn, unspecified Also known as: Low birth weight of newborn, unspecified | Low birth weight of newborn | birthweight low for gestational age | fetal malnutrition, light-for-dates | intrauterine or fetal malnutrition, light-for-dates [MB48.3] Light-headedness Also known as: Light-headedness | light headed [9D45] Impairment of light sensitivity Also known as: Impairment of light sensitivity | Vision sensitivity deficiencies | Day blindness | Impairment of dark adaptation | Moderate Impairment of Dark adaptation [GA20.51] Light menstrual bleeding Definition: Menstruation with light (< 5 ml) volume of monthly blood loss Also known as: Light menstrual bleeding | light menstrual period | scanty menses | scanty menstruation | scanty period [2A83.52] Light chain deposition disease Definition: A disease of the kidney, caused by the deposition of pieces of truncated or abnormal light chain segments of white blood cells. This disease is characterised by fibrillar or granular tissue deposits and renal dysfunction, which may lead to organ failure. Confirmation is by identification of light chain deposition tissue biopsy under an electron microscope. Also known as: Light chain deposition disease | systemic light chain disease Excludes: Immunodeficiencies with isotype or light chain deficiencies with normal number of B cells [9E1Z] Diseases of the visual system, unspecified Also known as: Diseases of the visual system, unspecified | eye diseases NOS | disorder of vision | visual disorder [MC1Y] Other specified symptoms or signs involving the visual system Also known as: Other specified symptoms or signs involving the visual system | Erythema of eyelid | Visual disturbances | disturbances of vision | difficulty seeing [9D9Z] Vision impairment, unspecified Also known as: Vision impairment, unspecified | sight impaired | blindness and low vision | impaired vision [9D90.2] Moderate vision impairment Also known as: Moderate vision impairment | low vision, both eyes | visual impairment category 2, in both eyes | Low vision | LW - [low vision] Includes: visual impairment category 2, in both eyes [QA00.6Z] Examination of eyes or vision, unspecified Also known as: Examination of eyes or vision, unspecified | Examination of eyes or vision | general eye examination | routine eye examination | vision examination === GRAPH WALKS === --- Walk 1 --- [KA21.2Z] Low birth weight of newborn, unspecified --PARENT--> [KA21.2] Low birth weight of newborn Def: A paediatric condition in which the infant is born weighing between 1500 and 2499 g.... --CHILD--> [KA21.2Z] Low birth weight of newborn, unspecified --- Walk 2 --- [KA21.2Z] Low birth weight of newborn, unspecified --PARENT--> [KA21.2] Low birth weight of newborn Def: A paediatric condition in which the infant is born weighing between 1500 and 2499 g.... --PARENT--> [KA21] Disorders of newborn related to short gestation or low birth weight, not elsewhere classified Def: Infants whose weight is appropriate for their gestational ages are termed appropriate for gestational age (AGA). Infants that are heavier than expected are large for gestational age (LGA). Conversely,... --- Walk 3 --- [MB48.3] Light-headedness --PARENT--> [MB48] Dizziness or giddiness Def: Terms which may refer to a sense of spatial disorientation, motion of the environment, or lightheadedness. Dizziness is a general feeling of being off-balance. Giddiness is the feeling that you or you... --CHILD--> [MB48.1] Disorder of equilibrium --- Walk 4 --- [MB48.3] Light-headedness --PARENT--> [MB48] Dizziness or giddiness Def: Terms which may refer to a sense of spatial disorientation, motion of the environment, or lightheadedness. Dizziness is a general feeling of being off-balance. Giddiness is the feeling that you or you... --CHILD--> [MB48.1] Disorder of equilibrium --- Walk 5 --- [9D45] Impairment of light sensitivity --PARENT--> [?] Impairment of visual functions --RELATED_TO--> [?] Impairment of electrophysiological functions --- Walk 6 --- [9D45] Impairment of light sensitivity --PARENT--> [?] Impairment of visual functions --CHILD--> [9D43] Impairment of contrast vision Def: Contrast sensitivity refers to the ability to distinguish small differences in brightness between adjacent surfaces. Peak Contrast sensitivity refers to the smallest differences that are discernible ...
[ "[KA21.2Z] Low birth weight of newborn, unspecified\n --PARENT--> [KA21.2] Low birth weight of newborn\n Def: A paediatric condition in which the infant is born weighing between 1500 and 2499 g....\n --CHILD--> [KA21.2Z] Low birth weight of newborn, unspecified", "[KA21.2Z] Low birth weight of newborn, unspecified\n --PARENT--> [KA21.2] Low birth weight of newborn\n Def: A paediatric condition in which the infant is born weighing between 1500 and 2499 g....\n --PARENT--> [KA21] Disorders of newborn related to short gestation or low birth weight, not elsewhere classified\n Def: Infants whose weight is appropriate for their gestational ages are termed appropriate for gestational age (AGA). Infants that are heavier than expected are large for gestational age (LGA). Conversely,...", "[MB48.3] Light-headedness\n --PARENT--> [MB48] Dizziness or giddiness\n Def: Terms which may refer to a sense of spatial disorientation, motion of the environment, or lightheadedness. Dizziness is a general feeling of being off-balance. Giddiness is the feeling that you or you...\n --CHILD--> [MB48.1] Disorder of equilibrium", "[MB48.3] Light-headedness\n --PARENT--> [MB48] Dizziness or giddiness\n Def: Terms which may refer to a sense of spatial disorientation, motion of the environment, or lightheadedness. Dizziness is a general feeling of being off-balance. Giddiness is the feeling that you or you...\n --CHILD--> [MB48.1] Disorder of equilibrium", "[9D45] Impairment of light sensitivity\n --PARENT--> [?] Impairment of visual functions\n --RELATED_TO--> [?] Impairment of electrophysiological functions", "[9D45] Impairment of light sensitivity\n --PARENT--> [?] Impairment of visual functions\n --CHILD--> [9D43] Impairment of contrast vision\n Def: Contrast sensitivity refers to the ability to distinguish small differences in brightness between adjacent surfaces.\n\nPeak Contrast sensitivity refers to the smallest differences that are discernible ..." ]
KA21.2Z
Low birth weight of newborn, unspecified
[ { "from_icd11": "KA21.2Z", "icd10_code": "P071", "icd10_title": "Other low birth weight newborn" }, { "from_icd11": "9D45", "icd10_code": "H538", "icd10_title": "Other visual disturbances" }, { "from_icd11": "9D45", "icd10_code": "H536", "icd10_title": "Night blindness" }, { "from_icd11": "2A83.52", "icd10_code": "D477", "icd10_title": "" }, { "from_icd11": "9E1Z", "icd10_code": "H5500", "icd10_title": "Unspecified nystagmus" }, { "from_icd11": "9E1Z", "icd10_code": "H5509", "icd10_title": "Other forms of nystagmus" }, { "from_icd11": "9E1Z", "icd10_code": "H5581", "icd10_title": "Saccadic eye movements" }, { "from_icd11": "9E1Z", "icd10_code": "H5501", "icd10_title": "Congenital nystagmus" }, { "from_icd11": "9E1Z", "icd10_code": "H5502", "icd10_title": "Latent nystagmus" }, { "from_icd11": "9E1Z", "icd10_code": "H5589", "icd10_title": "Other irregular eye movements" }, { "from_icd11": "9E1Z", "icd10_code": "H5503", "icd10_title": "Visual deprivation nystagmus" }, { "from_icd11": "9E1Z", "icd10_code": "H5504", "icd10_title": "Dissociated nystagmus" }, { "from_icd11": "9E1Z", "icd10_code": "H44522", "icd10_title": "Atrophy of globe, left eye" }, { "from_icd11": "9E1Z", "icd10_code": "H3552", "icd10_title": "Pigmentary retinal dystrophy" }, { "from_icd11": "9E1Z", "icd10_code": "E70331", "icd10_title": "Hermansky-Pudlak syndrome" } ]
P071
Other low birth weight newborn
A 19-year-old previously healthy pregnant (seventh week) lady presented to our emergency department (ED) complaining of vomiting, melena, abdominal pain, shortness of breath, and generalized weakness. She had episodic diarrhea and mild right upper quadrant pain during the two weeks, prior to her presentation to ED. She was not taking any regular medications except for prenatal vitamins. On physical examination, she had blood pressure of 101/50 mmHg, heart rate of 145 beats per minute (bpm), respiratory rate of 34 breaths per minute, temperature of 37.1°C, with signs of dehydration and right upper abdominal tenderness and fullness. Abdominal ultrasound showed a large heterogeneous mainly hypoechoic lesion in the right liver lobe, with a maximum dimension of about 10 cm and pelvic ultrasound revealed an absence of fetal heart activity while blood work showed a hemoglobin (Hb) level of 4 g/dL. After stabilizing the patient and performing blood transfusion (four units of packed RBCs and fresh frozen plasma), she underwent an upper GI endoscopy in which gastric and duodenal inflammation was found with multiple duodenal ulcers which were clear of malignant changes on biopsies. Additionally, no masses and no source of active bleeding were evident. A subsequent lower GI endoscopy was unremarkable. It is of note that the patient had no prior history or laboratory evidence of Helicobacter pylori infection.
3.761719
0.985352
sec[1]/p[0]
en
0.999996
PMC8938252
https://doi.org/10.7759/cureus.22370
[ "abdominal", "blood", "pain", "heart", "minute", "ultrasound", "endoscopy", "which", "duodenal", "previously" ]
[ { "code": "MD81.3", "title": "Acute abdomen" }, { "code": "JA01.0", "title": "Abdominal pregnancy" }, { "code": "ME04.Z", "title": "Ascites, unspecified" }, { "code": "NB51.0&XA3KX0", "title": "Laceration without foreign body of abdominal wall" }, { "code": "NB9Y", "title": "Other specified injuries to the abdomen, lower back, lumbar spine or pelvis" }, { "code": "3C0Z", "title": "Diseases of the blood or blood-forming organs, unspecified" }, { "code": "MF50.4Z", "title": "Haematuria, unspecified" }, { "code": "MA12.1", "title": "Finding of cocaine in blood" }, { "code": "MA12.4", "title": "Finding of steroid agent in blood" }, { "code": "MA12.2", "title": "Finding of hallucinogen in blood" } ]
=== ICD-11 CODES FOUND === [MD81.3] Acute abdomen Definition: A clinical syndrome with acute abdominal pain that is severe, and rapid onset. Acute abdomen may be caused by a variety of disorders, injuries, or diseases Also known as: Acute abdomen | acute abdominal pain syndrome | surgical abdomen | abdominal acute syndrome | severe abdomen pain [JA01.0] Abdominal pregnancy Definition: A condition characterised by implantation of the embryo within the peritoneal cavity during pregnancy. Also known as: Abdominal pregnancy | abdomen pregnancy | intraperitoneal pregnancy Excludes: Maternal care for viable fetus in abdominal pregnancy | Delivery of viable fetus in abdominal pregnancy [ME04.Z] Ascites, unspecified Also known as: Ascites, unspecified | Ascites | abdominal dropsy | hydrops abdominis | ascites NOS [NB9Y] Other specified injuries to the abdomen, lower back, lumbar spine or pelvis Also known as: Other specified injuries to the abdomen, lower back, lumbar spine or pelvis | Abdominal wall trauma | Injury of pelvic floor | pelvic floor blunt injury | pelvic floor blunt trauma [3C0Z] Diseases of the blood or blood-forming organs, unspecified Also known as: Diseases of the blood or blood-forming organs, unspecified | Blood, lymph or spleen disease | blood condition NOS | blood disorder NOS | bone marrow disease NOS [MF50.4Z] Haematuria, unspecified Also known as: Haematuria, unspecified | Haematuria | blood in urine | urinary blood | haematuria NOS [MA12.1] Finding of cocaine in blood Also known as: Finding of cocaine in blood | cocaine in blood [MA12.4] Finding of steroid agent in blood Also known as: Finding of steroid agent in blood | steroid in blood [MA12.2] Finding of hallucinogen in blood Also known as: Finding of hallucinogen in blood | hallucinogen in blood === GRAPH WALKS === --- Walk 1 --- [MD81.3] Acute abdomen Def: A clinical syndrome with acute abdominal pain that is severe, and rapid onset. Acute abdomen may be caused by a variety of disorders, injuries, or diseases... --PARENT--> [MD81] Abdominal or pelvic pain Def: Pain, an unpleasant distress sensation occurring in varying degrees of severity, received by nerve ending in the abdominal and pelvic region.... --EXCLUDES--> [?] Flatulence and related conditions Def: Production or presence of gas in the gastrointestinal tract which may be expelled through the anus and other conditions associated with the production or presence of gas in the GI tract.... --- Walk 2 --- [MD81.3] Acute abdomen Def: A clinical syndrome with acute abdominal pain that is severe, and rapid onset. Acute abdomen may be caused by a variety of disorders, injuries, or diseases... --PARENT--> [MD81] Abdominal or pelvic pain Def: Pain, an unpleasant distress sensation occurring in varying degrees of severity, received by nerve ending in the abdominal and pelvic region.... --EXCLUDES--> [?] Flatulence and related conditions Def: Production or presence of gas in the gastrointestinal tract which may be expelled through the anus and other conditions associated with the production or presence of gas in the GI tract.... --- Walk 3 --- [JA01.0] Abdominal pregnancy Def: A condition characterised by implantation of the embryo within the peritoneal cavity during pregnancy.... --EXCLUDES--> [?] Delivery of viable fetus in abdominal pregnancy Def: A condition caused by the development of a viable fetus to the culmination of the pregnancy period. This condition is characterised by parturition of a viable neonate from the abdominal cavity, at the... --PARENT--> [?] Other assisted single delivery --- Walk 4 --- [JA01.0] Abdominal pregnancy Def: A condition characterised by implantation of the embryo within the peritoneal cavity during pregnancy.... --PARENT--> [JA01] Ectopic pregnancy Def: Any condition characterised by implantation of the embryo outside the endometrium and endometrial cavity during pregnancy.... --PARENT--> [?] Abortive outcome of pregnancy Def: A group of conditions characterised by pregnancy which does not result in live offspring. These conditions include e.g. abortion, ectopic pregnancy or molar pregnancy.... --- Walk 5 --- [ME04.Z] Ascites, unspecified --PARENT--> [ME04] Ascites Def: Accumulation or retention of free fluid in the abdominal peritoneal cavity between the tissues lining the abdomen and abdominal organs. The fluid may be serous, haemorrhagic, or the result of inflamma... --CHILD--> [ME04.0] Fluid in peritoneal cavity --- Walk 6 --- [ME04.Z] Ascites, unspecified --PARENT--> [ME04] Ascites Def: Accumulation or retention of free fluid in the abdominal peritoneal cavity between the tissues lining the abdomen and abdominal organs. The fluid may be serous, haemorrhagic, or the result of inflamma... --CHILD--> [ME04.Z] Ascites, unspecified
[ "[MD81.3] Acute abdomen\n Def: A clinical syndrome with acute abdominal pain that is severe, and rapid onset. Acute abdomen may be caused by a variety of disorders, injuries, or diseases...\n --PARENT--> [MD81] Abdominal or pelvic pain\n Def: Pain, an unpleasant distress sensation occurring in varying degrees of severity, received by nerve ending in the abdominal and pelvic region....\n --EXCLUDES--> [?] Flatulence and related conditions\n Def: Production or presence of gas in the gastrointestinal tract which may be expelled through the anus and other conditions associated with the production or presence of gas in the GI tract....", "[MD81.3] Acute abdomen\n Def: A clinical syndrome with acute abdominal pain that is severe, and rapid onset. Acute abdomen may be caused by a variety of disorders, injuries, or diseases...\n --PARENT--> [MD81] Abdominal or pelvic pain\n Def: Pain, an unpleasant distress sensation occurring in varying degrees of severity, received by nerve ending in the abdominal and pelvic region....\n --EXCLUDES--> [?] Flatulence and related conditions\n Def: Production or presence of gas in the gastrointestinal tract which may be expelled through the anus and other conditions associated with the production or presence of gas in the GI tract....", "[JA01.0] Abdominal pregnancy\n Def: A condition characterised by implantation of the embryo within the peritoneal cavity during pregnancy....\n --EXCLUDES--> [?] Delivery of viable fetus in abdominal pregnancy\n Def: A condition caused by the development of a viable fetus to the culmination of the pregnancy period. This condition is characterised by parturition of a viable neonate from the abdominal cavity, at the...\n --PARENT--> [?] Other assisted single delivery", "[JA01.0] Abdominal pregnancy\n Def: A condition characterised by implantation of the embryo within the peritoneal cavity during pregnancy....\n --PARENT--> [JA01] Ectopic pregnancy\n Def: Any condition characterised by implantation of the embryo outside the endometrium and endometrial cavity during pregnancy....\n --PARENT--> [?] Abortive outcome of pregnancy\n Def: A group of conditions characterised by pregnancy which does not result in live offspring. These conditions include e.g. abortion, ectopic pregnancy or molar pregnancy....", "[ME04.Z] Ascites, unspecified\n --PARENT--> [ME04] Ascites\n Def: Accumulation or retention of free fluid in the abdominal peritoneal cavity between the tissues lining the abdomen and abdominal organs. The fluid may be serous, haemorrhagic, or the result of inflamma...\n --CHILD--> [ME04.0] Fluid in peritoneal cavity", "[ME04.Z] Ascites, unspecified\n --PARENT--> [ME04] Ascites\n Def: Accumulation or retention of free fluid in the abdominal peritoneal cavity between the tissues lining the abdomen and abdominal organs. The fluid may be serous, haemorrhagic, or the result of inflamma...\n --CHILD--> [ME04.Z] Ascites, unspecified" ]
MD81.3
Acute abdomen
[ { "from_icd11": "MD81.3", "icd10_code": "R100", "icd10_title": "Acute abdomen" }, { "from_icd11": "JA01.0", "icd10_code": "O0000", "icd10_title": "Abdominal pregnancy without intrauterine pregnancy" }, { "from_icd11": "JA01.0", "icd10_code": "O000", "icd10_title": "Abdominal pregnancy" }, { "from_icd11": "ME04.Z", "icd10_code": "R180", "icd10_title": "Malignant ascites" }, { "from_icd11": "ME04.Z", "icd10_code": "R18", "icd10_title": "Ascites" }, { "from_icd11": "3C0Z", "icd10_code": "D75A", "icd10_title": "Glucose-6-phosphate dehydrogenase (G6PD) deficiency without anemia" }, { "from_icd11": "3C0Z", "icd10_code": "D7581", "icd10_title": "Myelofibrosis" }, { "from_icd11": "3C0Z", "icd10_code": "D7582", "icd10_title": "Heparin induced thrombocytopenia (HIT)" }, { "from_icd11": "3C0Z", "icd10_code": "D7589", "icd10_title": "Other specified diseases of blood and blood-forming organs" }, { "from_icd11": "3C0Z", "icd10_code": "D759", "icd10_title": "Disease of blood and blood-forming organs, unspecified" }, { "from_icd11": "3C0Z", "icd10_code": "D763", "icd10_title": "Other histiocytosis syndromes" }, { "from_icd11": "3C0Z", "icd10_code": "Q899", "icd10_title": "Congenital malformation, unspecified" }, { "from_icd11": "3C0Z", "icd10_code": "III", "icd10_title": "" }, { "from_icd11": "3C0Z", "icd10_code": "D70-D77", "icd10_title": "" }, { "from_icd11": "3C0Z", "icd10_code": "D75", "icd10_title": "Other and unspecified diseases of blood and blood-forming organs" } ]
R100
Acute abdomen
In August 2020, the patient experienced symptoms of delayed urination, shortened urinary line and a sense of frequent urination urgency. A color Doppler ultrasound showed no enlargement of the prostate, regular edge, complete capsule, uneven distribution of light spots, and strong light spots. Urodynamics showed bladder outlet obstruction IV (moderate and severe obstruction). Computed tomography (CT) showed that there was no obvious abnormality in the small calcification of the prostate, bladder or bilateral ureteral pelvic segments. Prostate specific antigen (PSA), carcinoembryonic antigen, carbohydrate antigen 19–9 and other related cancer indicators were within the normal range. Because we originally thought it was “benign prostatic hyperplasia,” we performed transurethral plasma resection of the prostate. The postoperative pathology showed: (prostate) adenocarcinoma, part of the cell morphology showed signet-ring differentiation, combined with medical history, and immunohistochemistry, tendency to metastasize from colon carcinoma to the prostate, cancer in vessels and cancer invasion in nerve fasciculus . The patient was diagnosed with ascending colon cecal junction carcinoma with prostate metastasis. The stage was pT4aN2bM1a (IVA). Considering the clear source of colon carcinoma metastasis, we began palliative chemotherapy in December 2020, and local radiotherapy of the prostate in May 2021.
3.810547
0.985352
sec[0]/sec[0]/p[1]
en
0.999996
PMC10019226
https://doi.org/10.1097/MD.0000000000033308
[ "prostate", "antigen", "cancer", "colon", "carcinoma", "urination", "light", "spots", "bladder", "obstruction" ]
[ { "code": "GA90", "title": "Hyperplasia of prostate" }, { "code": "GA91.Z", "title": "Inflammatory or other diseases of prostate, unspecified" }, { "code": "GA91.Y", "title": "Other specified inflammatory or other diseases of prostate" }, { "code": "GA91.0", "title": "Chronic prostatitis" }, { "code": "MF40.1", "title": "Problems of the prostate" }, { "code": "1E51.Y", "title": "Other specified chronic viral hepatitis" }, { "code": "1E50.1", "title": "Acute hepatitis B" }, { "code": "MA14.1B", "title": "Prostate specific antigen positive" }, { "code": "9C61.22", "title": "Lens-induced secondary open-angle glaucoma" }, { "code": "4A01.11", "title": "Major histocompatibility complex class I deficiency" } ]
=== ICD-11 CODES FOUND === [GA90] Hyperplasia of prostate Definition: A condition of the prostate, caused by an increased rate of cellular division of the glandular and stromal cells. This condition is characterised by enlargement of the prostatic tissue, dysuria, urinary urgency, nocturia, weak urine stream, straining while urinating, incomplete bladder emptying during urination, or increased frequency of urinary tract infection. Also known as: Hyperplasia of prostate | Adenofibromatous hypertrophy of prostate | benign prostatic hyperplasia | prostate hyperplasia | prostatic area hypertrophy Includes: Adenofibromatous hypertrophy of prostate Excludes: Benign neoplasms of prostate [GA91.Z] Inflammatory or other diseases of prostate, unspecified Also known as: Inflammatory or other diseases of prostate, unspecified | Inflammatory or other diseases of prostate | inflammation of prostate NOS | prostatitis NOS | disease of prostate NOS [GA91.Y] Other specified inflammatory or other diseases of prostate Also known as: Other specified inflammatory or other diseases of prostate | Acute bacterial prostatitis | acute prostatitis | Prostatitis category I (NIH classification) | Prostatitis category I [GA91.0] Chronic prostatitis Definition: A condition caused by obstruction of the prostate glands. This condition is characterised by inflammation of the prostate gland, dysuria, pollakiuria, urinary urgency, genital pain, lower back pain, abdominal pain, and repeated bladder infections that last for at least three months. Also known as: Chronic prostatitis | Fibrous prostatitis | Hypertrophic prostatitis | Subacute prostatitis | Chronic bacterial prostatitis [MF40.1] Problems of the prostate Definition: A group of disorders associated with the prostate occurring in diseases more specifically classified elsewhere. Also known as: Problems of the prostate [1E51.Y] Other specified chronic viral hepatitis Also known as: Other specified chronic viral hepatitis | Carrier of viral hepatitis (obsolete concept) | carrier of hepatitis virus | Hepatitis B surface antigen [HBsAg] carrier | carrier of hepatitis b surface antigen [1E50.1] Acute hepatitis B Definition: Acute liver injury and inflammation caused by recent and short-term (less than 6 months) infection with hepatitis B virus (HBV). Transmission is by sexual, blood and body fluid contamination (parenteral spread), and from mother to baby at the time of birth (vertical transmission). Diagnosis is confirmed by presence of recent acquisition of HBsAg, ideally with IgM-anti-HBc in serum. Clinical features, if they occur, are characterised by anorexia, nausea and fever, with jaundice in severe cases. Also known as: Acute hepatitis B | Acute hepatitis B virus infection | Acute hepatitis B with Hepatitis D virus co-infection | acute hepatitis B with delta-agent without hepatic coma | acute hepatitis type B, with delta-agent [MA14.1B] Prostate specific antigen positive Also known as: Prostate specific antigen positive | PSA - [prostate specific antigen] | elevated PSA | increased prostatic specific antigen | Abnormality of prostate-specific antigen [PSA] [9C61.22] Lens-induced secondary open-angle glaucoma Also known as: Lens-induced secondary open-angle glaucoma | Phacolytic glaucoma | Lens particle induced glaucoma | Phacoantigenic glaucoma [4A01.11] Major histocompatibility complex class I deficiency Also known as: Major histocompatibility complex class I deficiency | Bare lymphocyte syndrome type 1 | Immunodeficiency by defective expression of HLA - [human leukocyte antigen] class 1 | SCID - [severe combined immunodeficiency] due to absent class 2 HLA antigens | BLS - [bare lymphocyte syndrome] NOS === GRAPH WALKS === --- Walk 1 --- [GA90] Hyperplasia of prostate Def: A condition of the prostate, caused by an increased rate of cellular division of the glandular and stromal cells. This condition is characterised by enlargement of the prostatic tissue, dysuria, urina... --PARENT--> [?] Diseases of prostate --RELATED_TO--> [?] Tuberculosis of prostate Def: This is a common, and in many cases lethal, infectious disease caused by various strains of mycobacteria, usually Mycobacterium tuberculosis. This diagnosis is of the prostate.... --- Walk 2 --- [GA90] Hyperplasia of prostate Def: A condition of the prostate, caused by an increased rate of cellular division of the glandular and stromal cells. This condition is characterised by enlargement of the prostatic tissue, dysuria, urina... --EXCLUDES--> [?] Benign neoplasm of male genital organs Def: A non-metastasizing neoplasm that arises from the male reproductive system. Representative examples include benign prostate phyllodes tumour, benign Sertoli cell tumour, seminal vesicle cystadenoma, a... --CHILD--> [?] Benign neoplasm of prostate Def: A non-metastasizing neoplasm that arises from the prostate. Representative examples include benign phyllodes tumour, leiomyoma, and fibroma.... --- Walk 3 --- [GA91.Z] Inflammatory or other diseases of prostate, unspecified --PARENT--> [GA91] Inflammatory or other diseases of prostate Def: Any disease caused by obstruction of the prostate gland. These diseases are characterised by a build-up of secretions and inflammation of the prostate.... --RELATED_TO--> [?] Prostatitis due to Trichomonas vaginalis Def: This refers to an inflammation of the prostate gland caused by an infection with the protozoan parasite Trichomonas vaginalis.... --- Walk 4 --- [GA91.Z] Inflammatory or other diseases of prostate, unspecified --PARENT--> [GA91] Inflammatory or other diseases of prostate Def: Any disease caused by obstruction of the prostate gland. These diseases are characterised by a build-up of secretions and inflammation of the prostate.... --RELATED_TO--> [?] Prostatitis due to Trichomonas vaginalis Def: This refers to an inflammation of the prostate gland caused by an infection with the protozoan parasite Trichomonas vaginalis.... --- Walk 5 --- [GA91.Y] Other specified inflammatory or other diseases of prostate --PARENT--> [GA91] Inflammatory or other diseases of prostate Def: Any disease caused by obstruction of the prostate gland. These diseases are characterised by a build-up of secretions and inflammation of the prostate.... --CHILD--> [GA91.0] Chronic prostatitis Def: A condition caused by obstruction of the prostate glands. This condition is characterised by inflammation of the prostate gland, dysuria, pollakiuria, urinary urgency, genital pain, lower back pain, a... --- Walk 6 --- [GA91.Y] Other specified inflammatory or other diseases of prostate --PARENT--> [GA91] Inflammatory or other diseases of prostate Def: Any disease caused by obstruction of the prostate gland. These diseases are characterised by a build-up of secretions and inflammation of the prostate.... --RELATED_TO--> [?] Gonococcal prostatitis
[ "[GA90] Hyperplasia of prostate\n Def: A condition of the prostate, caused by an increased rate of cellular division of the glandular and stromal cells. This condition is characterised by enlargement of the prostatic tissue, dysuria, urina...\n --PARENT--> [?] Diseases of prostate\n --RELATED_TO--> [?] Tuberculosis of prostate\n Def: This is a common, and in many cases lethal, infectious disease caused by various strains of mycobacteria, usually Mycobacterium tuberculosis. This diagnosis is of the prostate....", "[GA90] Hyperplasia of prostate\n Def: A condition of the prostate, caused by an increased rate of cellular division of the glandular and stromal cells. This condition is characterised by enlargement of the prostatic tissue, dysuria, urina...\n --EXCLUDES--> [?] Benign neoplasm of male genital organs\n Def: A non-metastasizing neoplasm that arises from the male reproductive system. Representative examples include benign prostate phyllodes tumour, benign Sertoli cell tumour, seminal vesicle cystadenoma, a...\n --CHILD--> [?] Benign neoplasm of prostate\n Def: A non-metastasizing neoplasm that arises from the prostate. Representative examples include benign phyllodes tumour, leiomyoma, and fibroma....", "[GA91.Z] Inflammatory or other diseases of prostate, unspecified\n --PARENT--> [GA91] Inflammatory or other diseases of prostate\n Def: Any disease caused by obstruction of the prostate gland. These diseases are characterised by a build-up of secretions and inflammation of the prostate....\n --RELATED_TO--> [?] Prostatitis due to Trichomonas vaginalis\n Def: This refers to an inflammation of the prostate gland caused by an infection with the protozoan parasite Trichomonas vaginalis....", "[GA91.Z] Inflammatory or other diseases of prostate, unspecified\n --PARENT--> [GA91] Inflammatory or other diseases of prostate\n Def: Any disease caused by obstruction of the prostate gland. These diseases are characterised by a build-up of secretions and inflammation of the prostate....\n --RELATED_TO--> [?] Prostatitis due to Trichomonas vaginalis\n Def: This refers to an inflammation of the prostate gland caused by an infection with the protozoan parasite Trichomonas vaginalis....", "[GA91.Y] Other specified inflammatory or other diseases of prostate\n --PARENT--> [GA91] Inflammatory or other diseases of prostate\n Def: Any disease caused by obstruction of the prostate gland. These diseases are characterised by a build-up of secretions and inflammation of the prostate....\n --CHILD--> [GA91.0] Chronic prostatitis\n Def: A condition caused by obstruction of the prostate glands. This condition is characterised by inflammation of the prostate gland, dysuria, pollakiuria, urinary urgency, genital pain, lower back pain, a...", "[GA91.Y] Other specified inflammatory or other diseases of prostate\n --PARENT--> [GA91] Inflammatory or other diseases of prostate\n Def: Any disease caused by obstruction of the prostate gland. These diseases are characterised by a build-up of secretions and inflammation of the prostate....\n --RELATED_TO--> [?] Gonococcal prostatitis" ]
GA90
Hyperplasia of prostate
[ { "from_icd11": "GA90", "icd10_code": "N402", "icd10_title": "Nodular prostate without lower urinary tract symptoms" }, { "from_icd11": "GA90", "icd10_code": "N403", "icd10_title": "Nodular prostate with lower urinary tract symptoms" }, { "from_icd11": "GA90", "icd10_code": "N400", "icd10_title": "Benign prostatic hyperplasia without lower urinary tract symptoms" }, { "from_icd11": "GA90", "icd10_code": "N401", "icd10_title": "Benign prostatic hyperplasia with lower urinary tract symptoms" }, { "from_icd11": "GA90", "icd10_code": "N40", "icd10_title": "Benign prostatic hyperplasia" }, { "from_icd11": "GA91.Z", "icd10_code": "N414", "icd10_title": "Granulomatous prostatitis" }, { "from_icd11": "GA91.Z", "icd10_code": "N4289", "icd10_title": "Other specified disorders of prostate" }, { "from_icd11": "GA91.Z", "icd10_code": "N4283", "icd10_title": "Cyst of prostate" }, { "from_icd11": "GA91.Z", "icd10_code": "N410", "icd10_title": "Acute prostatitis" }, { "from_icd11": "GA91.Z", "icd10_code": "N419", "icd10_title": "Inflammatory disease of prostate, unspecified" }, { "from_icd11": "GA91.Z", "icd10_code": "N429", "icd10_title": "Disorder of prostate, unspecified" }, { "from_icd11": "GA91.Z", "icd10_code": "N418", "icd10_title": "Other inflammatory diseases of prostate" }, { "from_icd11": "GA91.Z", "icd10_code": "N41", "icd10_title": "Inflammatory diseases of prostate" }, { "from_icd11": "GA91.Z", "icd10_code": "N42", "icd10_title": "Other and unspecified disorders of prostate" }, { "from_icd11": "GA91.Z", "icd10_code": "N428", "icd10_title": "Other specified disorders of prostate" } ]
N402
Nodular prostate without lower urinary tract symptoms
A 33-year-old female with a history of encephalomyelitis treated with high-dose methylprednisolone in 2018 presented with neutropenia and mild anaemia in November 2021. A month later, she developed a high fever, fatigue, headache, and pancytopenia with an absolute neutrophil count (ANC) of 0.3 × 10 9 /L, HGB of 93 g/L, and PLT of 37 × 10 9 /L . The CRP level was 131 mg/L (normal: 0-8 mg/L) . She was admitted to our hospital. Bone marrow aspiration and biopsy demonstrated haemophagocytosis. Flow cytometric (FC) analysis of bone marrow showed no clonal abnormalities, and chromosome karyotype analysis was normal. The laboratory data revealed abnormal liver function with an ALT of 70 units/L, AST of 182 units/L, and TBil of 24 µmol/L. Coagulation detection showed a decreased level of fibrinogen (0.25 g/L) and prolonged APTT (75.4 s) . Her ferritin level was 12459 µg/L and the TG level (7.04 mmol/L) was four times higher than normal . EBV-DNA in blood plasma was 896.68 copies/ml (normal: <400 copies/ml). EBV nuclear antigen IgG (EBNA-IgG) and EBV capsid antigen IgG (EBCA-IgG) antibody titers were 235 U/ml (normal: < 5 U/ml) and 218 U/ml (normal: < 20 U/ml), respectively. Abdominal CT showed splenomegaly. The patient denied that she had repeatedly developed HLH and denied a family history of HLH. According to her clinical manifestations and laboratory parameters, she was diagnosed with HLH ( Table 1 ).
4.09375
0.96582
sec[1]/sec[1]/p[0]
en
0.999997
PMC10029757
https://doi.org/10.3389/fonc.2023.1054175
[ "bone", "marrow", "laboratory", "copies", "antigen", "denied", "encephalomyelitis", "treated", "methylprednisolone", "neutropenia" ]
[ { "code": "FC0Z", "title": "Diseases of the musculoskeletal system or connective tissue, unspecified" }, { "code": "FB84.Z", "title": "Osteomyelitis or osteitis, unspecified" }, { "code": "FB80.Z", "title": "Disorder of bone density or structure, unspecified" }, { "code": "FB86.11", "title": "Hypertrophy of bone" }, { "code": "FB86.1Z", "title": "Bone hyperplasias, unspecified" }, { "code": "3C0Z", "title": "Diseases of the blood or blood-forming organs, unspecified" }, { "code": "3A70.Z", "title": "Aplastic anaemia, unspecified" }, { "code": "3C0Y", "title": "Other specified diseases of the blood or blood-forming organs" }, { "code": "3A70.12", "title": "Idiopathic aplastic anaemia" }, { "code": "NE84", "title": "Failure or rejection of transplanted organs or tissues" } ]
=== ICD-11 CODES FOUND === [FC0Z] Diseases of the musculoskeletal system or connective tissue, unspecified Also known as: Diseases of the musculoskeletal system or connective tissue, unspecified | bone disease NOS | bone disorder NOS | bone lesion NOS | musculoskeletal complications NOS [FB84.Z] Osteomyelitis or osteitis, unspecified Also known as: Osteomyelitis or osteitis, unspecified | Osteomyelitis or osteitis | bone inflammation | bone ulcer | bone inflammatory disease [FB80.Z] Disorder of bone density or structure, unspecified Also known as: Disorder of bone density or structure, unspecified | Certain specified disorders of bone density or structure [FB86.11] Hypertrophy of bone Also known as: Hypertrophy of bone | bone thickening | periosteum thickening | Infantile cortical hyperostoses | Post traumatic subperiosteal ossification [FB86.1Z] Bone hyperplasias, unspecified Also known as: Bone hyperplasias, unspecified | Bone hyperplasias [3C0Z] Diseases of the blood or blood-forming organs, unspecified Also known as: Diseases of the blood or blood-forming organs, unspecified | Blood, lymph or spleen disease | blood condition NOS | blood disorder NOS | bone marrow disease NOS [3A70.Z] Aplastic anaemia, unspecified Also known as: Aplastic anaemia, unspecified | Aplastic anaemia | erythroid aplasia | AA - [aplastic anaemia] | haematopoietic aplasia [3C0Y] Other specified diseases of the blood or blood-forming organs Also known as: Other specified diseases of the blood or blood-forming organs | Congenital anomaly blood or lymph other | Blood dyscrasia | blood dyscrasia NOS | Bone marrow hyperplasia [3A70.12] Idiopathic aplastic anaemia Also known as: Idiopathic aplastic anaemia | Idiopathic bone marrow failure | idiopathic aplastic anaemia NOS [NE84] Failure or rejection of transplanted organs or tissues Also known as: Failure or rejection of transplanted organs or tissues | organ transplant rejection | transplant failure | transplant rejection | Bone-marrow transplant rejection === GRAPH WALKS === --- Walk 1 --- [FC0Z] Diseases of the musculoskeletal system or connective tissue, unspecified --PARENT--> [15] Diseases of the musculoskeletal system or connective tissue Def: This chapter contains diseases of musculoskeletal system and diseases of connective tissue.... --EXCLUDES--> [?] Endocrine, nutritional or metabolic diseases Def: This chapter includes endocrine diseases, nutritional diseases as well as metabolic diseases.... --- Walk 2 --- [FC0Z] Diseases of the musculoskeletal system or connective tissue, unspecified --PARENT--> [15] Diseases of the musculoskeletal system or connective tissue Def: This chapter contains diseases of musculoskeletal system and diseases of connective tissue.... --PARENT--> [?] ICD-11 for Mortality and Morbidity Statistics --- Walk 3 --- [FB84.Z] Osteomyelitis or osteitis, unspecified --PARENT--> [FB84] Osteomyelitis or osteitis --CHILD--> [FB84.2] Subacute osteomyelitis --- Walk 4 --- [FB84.Z] Osteomyelitis or osteitis, unspecified --PARENT--> [FB84] Osteomyelitis or osteitis --EXCLUDES--> [?] Inflammatory conditions of jaws --- Walk 5 --- [FB80.Z] Disorder of bone density or structure, unspecified --PARENT--> [FB80] Certain specified disorders of bone density or structure --EXCLUDES--> [?] Osteopetrosis Def: Osteopetrosis ('marble bone disease') is a descriptive term that refers to a group of rare, heritable disorders of the skeleton characterised by increased bone density on radiographs. Osteopetrotic co... --- Walk 6 --- [FB80.Z] Disorder of bone density or structure, unspecified --PARENT--> [FB80] Certain specified disorders of bone density or structure --CHILD--> [FB80.1] Skeletal fluorosis
[ "[FC0Z] Diseases of the musculoskeletal system or connective tissue, unspecified\n --PARENT--> [15] Diseases of the musculoskeletal system or connective tissue\n Def: This chapter contains diseases of musculoskeletal system and diseases of connective tissue....\n --EXCLUDES--> [?] Endocrine, nutritional or metabolic diseases\n Def: This chapter includes endocrine diseases, nutritional diseases as well as metabolic diseases....", "[FC0Z] Diseases of the musculoskeletal system or connective tissue, unspecified\n --PARENT--> [15] Diseases of the musculoskeletal system or connective tissue\n Def: This chapter contains diseases of musculoskeletal system and diseases of connective tissue....\n --PARENT--> [?] ICD-11 for Mortality and Morbidity Statistics", "[FB84.Z] Osteomyelitis or osteitis, unspecified\n --PARENT--> [FB84] Osteomyelitis or osteitis\n --CHILD--> [FB84.2] Subacute osteomyelitis", "[FB84.Z] Osteomyelitis or osteitis, unspecified\n --PARENT--> [FB84] Osteomyelitis or osteitis\n --EXCLUDES--> [?] Inflammatory conditions of jaws", "[FB80.Z] Disorder of bone density or structure, unspecified\n --PARENT--> [FB80] Certain specified disorders of bone density or structure\n --EXCLUDES--> [?] Osteopetrosis\n Def: Osteopetrosis ('marble bone disease') is a descriptive term that refers to a group of rare, heritable disorders of the skeleton characterised by increased bone density on radiographs. Osteopetrotic co...", "[FB80.Z] Disorder of bone density or structure, unspecified\n --PARENT--> [FB80] Certain specified disorders of bone density or structure\n --CHILD--> [FB80.1] Skeletal fluorosis" ]
FC0Z
Diseases of the musculoskeletal system or connective tissue, unspecified
[ { "from_icd11": "FC0Z", "icd10_code": "XIII", "icd10_title": "" }, { "from_icd11": "FB84.Z", "icd10_code": "M86672", "icd10_title": "Other chronic osteomyelitis, left ankle and foot" }, { "from_icd11": "FB84.Z", "icd10_code": "M86172", "icd10_title": "Other acute osteomyelitis, left ankle and foot" }, { "from_icd11": "FB84.Z", "icd10_code": "M86171", "icd10_title": "Other acute osteomyelitis, right ankle and foot" }, { "from_icd11": "FB84.Z", "icd10_code": "M86671", "icd10_title": "Other chronic osteomyelitis, right ankle and foot" }, { "from_icd11": "FB84.Z", "icd10_code": "M868X7", "icd10_title": "Other osteomyelitis, ankle and foot" }, { "from_icd11": "FB84.Z", "icd10_code": "M868X8", "icd10_title": "Other osteomyelitis, other site" }, { "from_icd11": "FB84.Z", "icd10_code": "M868X6", "icd10_title": "Other osteomyelitis, lower leg" }, { "from_icd11": "FB84.Z", "icd10_code": "M868X9", "icd10_title": "Other osteomyelitis, unspecified sites" }, { "from_icd11": "FB84.Z", "icd10_code": "M8668", "icd10_title": "Other chronic osteomyelitis, other site" }, { "from_icd11": "FB84.Z", "icd10_code": "M86662", "icd10_title": "Other chronic osteomyelitis, left tibia and fibula" }, { "from_icd11": "FB84.Z", "icd10_code": "M86151", "icd10_title": "Other acute osteomyelitis, right femur" }, { "from_icd11": "FB84.Z", "icd10_code": "M86141", "icd10_title": "Other acute osteomyelitis, right hand" }, { "from_icd11": "FB84.Z", "icd10_code": "M86641", "icd10_title": "Other chronic osteomyelitis, right hand" }, { "from_icd11": "FB84.Z", "icd10_code": "M8669", "icd10_title": "Other chronic osteomyelitis, multiple sites" } ]
XIII
A 60-year-old man on oral medication for diabetes, hypertension, and hyperlipidemia, including clopidogrel, underwent demarcation laser treatment for retinal holes of OU in 2010. He received the first dose of AZ on June 14, 2021. Two days later, he developed an occipital headache and binocular horizontal diplopia when looking straight ahead or to the right. He was admitted to the emergency room on June 18, 2021. His BCVAs were 0.8 both for the OD and OS, and his IOPs were 13 mmHg both for the OD and OS. There was no EOM limitation, but left superior oblique underaction (SOUA) was present . He had exotropia of 4 PD with OS deviation in the primary position, right gaze, and left gaze. Left hypertropia of 4 PD occurred only when he looked to the right. His head was tilted to the right at rest, and the diplopia was aggravated when he tilted his head to the left. A right distal internal carotid artery aneurysm was observed on brain MRI, which was an incidental finding that did not correlate with the symptoms. The patient was considered to have left fourth nerve palsy, and he continued taking clopidogrel and undergoing outpatient follow-up. Fig. 2 Hess screen tests and eye movements in case 6, demonstrating left fourth nerve palsy. a Nine cardinal gaze directions showing left superior oblique underaction on day 3. b Hess screen test on day 15. c Hess screen test on week 7. d Hess screen test on week 20
3.855469
0.984375
sec[2]/sec[5]/p[0]
en
0.999997
PMC9813886
https://doi.org/10.1186/s12886-022-02747-7
[ "hess", "screen", "gaze", "clopidogrel", "june", "diplopia", "both", "oblique", "underaction", "head" ]
[ { "code": "QA0A.Z", "title": "Special screening examination for other diseases or disorders, unspecified" }, { "code": "QA04.0", "title": "Blood-alcohol or blood-drug test" }, { "code": "QA09.Z", "title": "Special screening for neoplasm of unspecified site" }, { "code": "QA0A.3", "title": "Special screening examination for mental or behavioural disorders" }, { "code": "QA08.6", "title": "Special screening examination for other protozoal diseases or helminthiases" }, { "code": "9C83.01", "title": "Vertical gaze palsy" }, { "code": "9D51", "title": "Transient visual loss" }, { "code": "9C83.1Z", "title": "Spasm of conjugate gaze, unspecified" }, { "code": "9C83.11", "title": "Upward gaze deviation" }, { "code": "9C83.10", "title": "Horizontal conjugate gaze deviation" } ]
=== ICD-11 CODES FOUND === [QA0A.Z] Special screening examination for other diseases or disorders, unspecified Also known as: Special screening examination for other diseases or disorders, unspecified | Special screening examination for other diseases or disorders | special screening NOS | screening NOS | multiphasic screening [QA04.0] Blood-alcohol or blood-drug test Also known as: Blood-alcohol or blood-drug test | blood alcohol test | blood drug test | screening for drugs | screening for hormones Excludes: Finding of alcohol in blood | presence of drugs in blood [QA09.Z] Special screening for neoplasm of unspecified site Also known as: Special screening for neoplasm of unspecified site | Special screening examination for neoplasms | neoplasm screening | Special screening examination for neoplasm, unspecified [QA0A.3] Special screening examination for mental or behavioural disorders Also known as: Special screening examination for mental or behavioural disorders | developmental handicap screening | screening for behavioural disorder | Screening for alcoholism | Screening for depression [QA08.6] Special screening examination for other protozoal diseases or helminthiases Also known as: Special screening examination for other protozoal diseases or helminthiases | screening for helminthiasis | screening for protozoal disease | Filariasis screening | Leishmaniasis screening Excludes: Protozoal intestinal infections [9C83.01] Vertical gaze palsy Definition: A palsy of vertical gaze is an incomplete or absent movement of the two eyes in the vertical direction of gaze. Also known as: Vertical gaze palsy | Paralysis of downgaze | Paralysis of upgaze | Paralysis of combined upgaze and downgaze | Vertical one-and-a-half syndrome [9D51] Transient visual loss Also known as: Transient visual loss | transient blindness | Transient vision loss, type not specified | Transient vision loss, induced | Uthoff, gaze [9C83.1Z] Spasm of conjugate gaze, unspecified Also known as: Spasm of conjugate gaze, unspecified | Spasm of conjugate gaze | conjugate deviation of the eyes | Conjugate gaze deviation [9C83.11] Upward gaze deviation Also known as: Upward gaze deviation | Sustained upward gaze deviation | Sustained tonic upward gaze deviation | Intermittent upward gaze deviation | Paroxysmal tonic upgaze of childhood with ataxia [9C83.10] Horizontal conjugate gaze deviation Also known as: Horizontal conjugate gaze deviation | Sustained horizontal conjugate gaze deviation | Sustained horizontal conjugate gaze deviation, ipsilateral type | Sustained horizontal conjugate gaze deviation, contralateral type | Sustained tonic horizontal conjugate gaze deviation === GRAPH WALKS === --- Walk 1 --- [QA0A.Z] Special screening examination for other diseases or disorders, unspecified --PARENT--> [QA0A] Special screening examination for other diseases or disorders --PARENT--> [?] Contact with health services for purposes of examination or investigation --- Walk 2 --- [QA0A.Z] Special screening examination for other diseases or disorders, unspecified --PARENT--> [QA0A] Special screening examination for other diseases or disorders --CHILD--> [QA0A.0] Special screening examination for diseases of the blood or blood-forming organs or certain disorders involving the immune mechanism --- Walk 3 --- [QA04.0] Blood-alcohol or blood-drug test --PARENT--> [QA04] Examination or observation for reasons other than suspected diseases or conditions or administrative purposes --CHILD--> [QA04.1] Alcohol and drug testing other than by blood --- Walk 4 --- [QA04.0] Blood-alcohol or blood-drug test --EXCLUDES--> [?] Finding of alcohol in blood --PARENT--> [?] Clinical findings of substances chiefly nonmedicinal as to source in blood, blood-forming organs, or the immune system --- Walk 5 --- [QA09.Z] Special screening for neoplasm of unspecified site --PARENT--> [QA09] Special screening examination for neoplasms --CHILD--> [QA09.1] Special screening examination for neoplasm of intestinal tract --- Walk 6 --- [QA09.Z] Special screening for neoplasm of unspecified site --PARENT--> [QA09] Special screening examination for neoplasms --CHILD--> [QA09.0] Special screening examination for neoplasm of stomach
[ "[QA0A.Z] Special screening examination for other diseases or disorders, unspecified\n --PARENT--> [QA0A] Special screening examination for other diseases or disorders\n --PARENT--> [?] Contact with health services for purposes of examination or investigation", "[QA0A.Z] Special screening examination for other diseases or disorders, unspecified\n --PARENT--> [QA0A] Special screening examination for other diseases or disorders\n --CHILD--> [QA0A.0] Special screening examination for diseases of the blood or blood-forming organs or certain disorders involving the immune mechanism", "[QA04.0] Blood-alcohol or blood-drug test\n --PARENT--> [QA04] Examination or observation for reasons other than suspected diseases or conditions or administrative purposes\n --CHILD--> [QA04.1] Alcohol and drug testing other than by blood", "[QA04.0] Blood-alcohol or blood-drug test\n --EXCLUDES--> [?] Finding of alcohol in blood\n --PARENT--> [?] Clinical findings of substances chiefly nonmedicinal as to source in blood, blood-forming organs, or the immune system", "[QA09.Z] Special screening for neoplasm of unspecified site\n --PARENT--> [QA09] Special screening examination for neoplasms\n --CHILD--> [QA09.1] Special screening examination for neoplasm of intestinal tract", "[QA09.Z] Special screening for neoplasm of unspecified site\n --PARENT--> [QA09] Special screening examination for neoplasms\n --CHILD--> [QA09.0] Special screening examination for neoplasm of stomach" ]
QA0A.Z
Special screening examination for other diseases or disorders, unspecified
[ { "from_icd11": "QA0A.Z", "icd10_code": "Z13850", "icd10_title": "Encounter for screening for traumatic brain injury" }, { "from_icd11": "QA0A.Z", "icd10_code": "Z13858", "icd10_title": "Encounter for screening for other nervous system disorders" }, { "from_icd11": "QA0A.Z", "icd10_code": "Z1389", "icd10_title": "Encounter for screening for other disorder" }, { "from_icd11": "QA0A.Z", "icd10_code": "Z1379", "icd10_title": "Encounter for other screening for genetic and chromosomal anomalies" }, { "from_icd11": "QA0A.Z", "icd10_code": "Z13", "icd10_title": "Encounter for screening for other diseases and disorders" }, { "from_icd11": "QA0A.Z", "icd10_code": "Z137", "icd10_title": "Encounter for screening for genetic and chromosomal anomalies" }, { "from_icd11": "QA0A.Z", "icd10_code": "Z138", "icd10_title": "Encounter for screening for other specified diseases and disorders" }, { "from_icd11": "QA0A.Z", "icd10_code": "Z139", "icd10_title": "Encounter for screening, unspecified" }, { "from_icd11": "QA04.0", "icd10_code": "Z040", "icd10_title": "" }, { "from_icd11": "QA09.Z", "icd10_code": "Z1289", "icd10_title": "Encounter for screening for malignant neoplasm of other sites" }, { "from_icd11": "QA09.Z", "icd10_code": "Z129", "icd10_title": "Encounter for screening for malignant neoplasm, site unspecified" }, { "from_icd11": "QA09.Z", "icd10_code": "Z12", "icd10_title": "Encounter for screening for malignant neoplasms" }, { "from_icd11": "QA09.Z", "icd10_code": "Z128", "icd10_title": "Encounter for screening for malignant neoplasm of other sites" }, { "from_icd11": "QA0A.3", "icd10_code": "Z133", "icd10_title": "Encounter for screening examination for mental health and behavioral disorders" }, { "from_icd11": "QA08.6", "icd10_code": "Z116", "icd10_title": "Encounter for screening for other protozoal diseases and helminthiases" } ]
Z13850
Encounter for screening for traumatic brain injury
Many authors suggest that pediatric and adolescent patients with fibroadenomas, presenting typical findings, both clinical and ultrasonographic, can be managed conservatively rather than surgically. The surgical excision of a fibroadenoma can cause scarring at the incision site, dimpling of the breast, duct system damage, and ultimately mammographic post-surgical changes that lower the diagnostic accuracy of mammography later in life. In addition, a recurrence is expected in 10–25% of the patients . In cases managed conservatively, a safe management option is to regularly follow up the mass with ultrasound in order to confirm the stability of the lesion over time. For those who desire a definite confirmation of the diagnosis, fine-needle aspiration or core needle biopsy can be offered . However, if the surgical excision of the mass has been decided, a core needle biopsy or other invasive testing methods prior to the operation should be avoided, since pediatric patients do not easily tolerate invasive procedures that may negatively impact them psychologically and emotionally. In our case, core biopsy was not performed since surgical resection was the optimal treatment method upon diagnosis, due to the rapid growth pattern of the mass and the presence of internal vascularity in ultrasound, and an additional invasive procedure, such as core biopsy, would not alter the surgical plan for this patient.
4.144531
0.349854
sec[3]/p[4]
en
0.999995
PMC10003210
https://doi.org/10.3390/jcm12051855
[ "core", "biopsy", "that", "patients", "needle", "invasive", "pediatric", "managed", "conservatively", "excision" ]
[ { "code": "8C72.02", "title": "Central core disease" }, { "code": "8C72.0Y", "title": "Other specified congenital myopathy with structural abnormalities" }, { "code": "JA85.Y", "title": "Maternal care for other specified fetal abnormality or damage" }, { "code": "KD39.3", "title": "Fetus or newborn affected by complications of fetal surgery" }, { "code": "PK81.5", "title": "Biopsy procedure, not elsewhere classified, associated with injury or harm in therapeutic use" }, { "code": "PK81.4", "title": "Bone marrow aspiration or biopsy associated with injury or harm in therapeutic use" }, { "code": "PK98.0", "title": "Radiological devices associated with injury or harm, diagnostic or monitoring devices" }, { "code": "8A80.Z", "title": "Migraine, unspecified" }, { "code": "QA76", "title": "Medication or substance that is known to be an allergen without injury or harm" }, { "code": "PL13.6", "title": "Medication or substance that is known to be an allergen, as mode of injury or harm" } ]
=== ICD-11 CODES FOUND === [8C72.02] Central core disease Definition: Central core disease (CCD) is an inherited neuromuscular disorder characterised by central cores on muscle biopsy and clinical features of a congenital myopathy (hypotonia and motor developmental delay) and is characterised by predominantly proximal weakness, pronounced in the hip girdle. Also known as: Central core disease [8C72.0Y] Other specified congenital myopathy with structural abnormalities Also known as: Other specified congenital myopathy with structural abnormalities | Congenital myopathy with excess of thin filaments | Actin myopathy | Myopathy with hexagonally cross-linked tubular arrays | Cap disease [JA85.Y] Maternal care for other specified fetal abnormality or damage Also known as: Maternal care for other specified fetal abnormality or damage | Maternal care for damage to fetus from alcohol | suspected damage to fetus from maternal alcohol addiction affecting management of mother | pregnancy management affected by fetal damage from maternal alcohol addiction | maternal care for known or suspected damage to fetus from alcohol [KD39.3] Fetus or newborn affected by complications of fetal surgery Definition: A condition in the fetus due to an unfavourable evolution of a condition (complication) associated with a surgical health intervention applied to the fetus. Also known as: Fetus or newborn affected by complications of fetal surgery | Adverse outcome following fetal skin biopsy [PK81.5] Biopsy procedure, not elsewhere classified, associated with injury or harm in therapeutic use Also known as: Biopsy procedure, not elsewhere classified, associated with injury or harm in therapeutic use | complication during or following biopsy procedure, other than bone marrow Excludes: Bone marrow aspiration or biopsy associated with injury or harm in therapeutic use | Circumstances associated with a surgical or other medical procedure influencing the episode of care, without injury or harm [PK81.4] Bone marrow aspiration or biopsy associated with injury or harm in therapeutic use Also known as: Bone marrow aspiration or biopsy associated with injury or harm in therapeutic use | complication during or following bone marrow aspiration or biopsy Excludes: Circumstances associated with a surgical or other medical procedure influencing the episode of care, without injury or harm [PK98.0] Radiological devices associated with injury or harm, diagnostic or monitoring devices Also known as: Radiological devices associated with injury or harm, diagnostic or monitoring devices | Radiological devices associated with adverse incidents, malfunction of radiological apparatus | Radiological devices associated with adverse incidents, CT scanner or MRI causing physical injury | Radiological devices associated with adverse incidents, needles used in radiologically-guided biopsies Excludes: Circumstances associated with a surgical or other medical device influencing the episode of care without injury or harm [8A80.Z] Migraine, unspecified Also known as: Migraine, unspecified | Migraine [QA76] Medication or substance that is known to be an allergen without injury or harm Definition: Medication that has previously been identified as an allergen to the patient is administered, but does not result in injury or harm. Also known as: Medication or substance that is known to be an allergen without injury or harm Excludes: Medication or substance that is known to be an allergen, as mode of injury or harm [PL13.6] Medication or substance that is known to be an allergen, as mode of injury or harm Also known as: Medication or substance that is known to be an allergen, as mode of injury or harm | medication error relating to known allergy to drug or substance | adverse drug event relating to known allergy to drug or substance === GRAPH WALKS === --- Walk 1 --- [8C72.02] Central core disease Def: Central core disease (CCD) is an inherited neuromuscular disorder characterised by central cores on muscle biopsy and clinical features of a congenital myopathy (hypotonia and motor developmental dela... --PARENT--> [8C72.0] Congenital myopathy with structural abnormalities Def: Distinct group of inherited disorders of skeletal muscles which have characteristic structural abnormalities on muscle immuno-histochemistry.... --EXCLUDES--> [?] Secondary myopathies Def: This is a group of conditions in which the muscle fibres are dysfunctional, resulting in muscle weakness. The myopathy is caused by an underlying disorder.... --- Walk 2 --- [8C72.02] Central core disease Def: Central core disease (CCD) is an inherited neuromuscular disorder characterised by central cores on muscle biopsy and clinical features of a congenital myopathy (hypotonia and motor developmental dela... --PARENT--> [8C72.0] Congenital myopathy with structural abnormalities Def: Distinct group of inherited disorders of skeletal muscles which have characteristic structural abnormalities on muscle immuno-histochemistry.... --CHILD--> [8C72.02] Central core disease Def: Central core disease (CCD) is an inherited neuromuscular disorder characterised by central cores on muscle biopsy and clinical features of a congenital myopathy (hypotonia and motor developmental dela... --- Walk 3 --- [8C72.0Y] Other specified congenital myopathy with structural abnormalities --PARENT--> [8C72.0] Congenital myopathy with structural abnormalities Def: Distinct group of inherited disorders of skeletal muscles which have characteristic structural abnormalities on muscle immuno-histochemistry.... --CHILD--> [8C72.00] Nemaline myopathy Def: Nemaline myopathy encompasses a large spectrum of congenital myopathies characterised by hypotonia, weakness and depressed or absent deep tendon reflexes, with pathologic evidence of nemaline bodies (... --- Walk 4 --- [8C72.0Y] Other specified congenital myopathy with structural abnormalities --PARENT--> [8C72.0] Congenital myopathy with structural abnormalities Def: Distinct group of inherited disorders of skeletal muscles which have characteristic structural abnormalities on muscle immuno-histochemistry.... --CHILD--> [8C72.02] Central core disease Def: Central core disease (CCD) is an inherited neuromuscular disorder characterised by central cores on muscle biopsy and clinical features of a congenital myopathy (hypotonia and motor developmental dela... --- Walk 5 --- [JA85.Y] Maternal care for other specified fetal abnormality or damage --PARENT--> [JA85] Maternal care for fetal abnormality or damage Def: A condition characterised by the provision of health interventions to the mother due to some abnormality or damage that is either suspected or known to be present in the fetus.... --EXCLUDES--> [?] Maternal care for disproportion Def: A condition characterised by the provision of health interventions to the mother due to the situation in which the head or body of the fetus is too large to fit through the pelvis of the mother.... --- Walk 6 --- [JA85.Y] Maternal care for other specified fetal abnormality or damage --PARENT--> [JA85] Maternal care for fetal abnormality or damage Def: A condition characterised by the provision of health interventions to the mother due to some abnormality or damage that is either suspected or known to be present in the fetus.... --CHILD--> [JA85.0] Maternal care for central nervous system malformation in fetus
[ "[8C72.02] Central core disease\n Def: Central core disease (CCD) is an inherited neuromuscular disorder characterised by central cores on muscle biopsy and clinical features of a congenital myopathy (hypotonia and motor developmental dela...\n --PARENT--> [8C72.0] Congenital myopathy with structural abnormalities\n Def: Distinct group of inherited disorders of skeletal muscles which have characteristic structural abnormalities on muscle immuno-histochemistry....\n --EXCLUDES--> [?] Secondary myopathies\n Def: This is a group of conditions in which the muscle fibres are dysfunctional, resulting in muscle weakness. The myopathy is caused by an underlying disorder....", "[8C72.02] Central core disease\n Def: Central core disease (CCD) is an inherited neuromuscular disorder characterised by central cores on muscle biopsy and clinical features of a congenital myopathy (hypotonia and motor developmental dela...\n --PARENT--> [8C72.0] Congenital myopathy with structural abnormalities\n Def: Distinct group of inherited disorders of skeletal muscles which have characteristic structural abnormalities on muscle immuno-histochemistry....\n --CHILD--> [8C72.02] Central core disease\n Def: Central core disease (CCD) is an inherited neuromuscular disorder characterised by central cores on muscle biopsy and clinical features of a congenital myopathy (hypotonia and motor developmental dela...", "[8C72.0Y] Other specified congenital myopathy with structural abnormalities\n --PARENT--> [8C72.0] Congenital myopathy with structural abnormalities\n Def: Distinct group of inherited disorders of skeletal muscles which have characteristic structural abnormalities on muscle immuno-histochemistry....\n --CHILD--> [8C72.00] Nemaline myopathy\n Def: Nemaline myopathy encompasses a large spectrum of congenital myopathies characterised by hypotonia, weakness and depressed or absent deep tendon reflexes, with pathologic evidence of nemaline bodies (...", "[8C72.0Y] Other specified congenital myopathy with structural abnormalities\n --PARENT--> [8C72.0] Congenital myopathy with structural abnormalities\n Def: Distinct group of inherited disorders of skeletal muscles which have characteristic structural abnormalities on muscle immuno-histochemistry....\n --CHILD--> [8C72.02] Central core disease\n Def: Central core disease (CCD) is an inherited neuromuscular disorder characterised by central cores on muscle biopsy and clinical features of a congenital myopathy (hypotonia and motor developmental dela...", "[JA85.Y] Maternal care for other specified fetal abnormality or damage\n --PARENT--> [JA85] Maternal care for fetal abnormality or damage\n Def: A condition characterised by the provision of health interventions to the mother due to some abnormality or damage that is either suspected or known to be present in the fetus....\n --EXCLUDES--> [?] Maternal care for disproportion\n Def: A condition characterised by the provision of health interventions to the mother due to the situation in which the head or body of the fetus is too large to fit through the pelvis of the mother....", "[JA85.Y] Maternal care for other specified fetal abnormality or damage\n --PARENT--> [JA85] Maternal care for fetal abnormality or damage\n Def: A condition characterised by the provision of health interventions to the mother due to some abnormality or damage that is either suspected or known to be present in the fetus....\n --CHILD--> [JA85.0] Maternal care for central nervous system malformation in fetus" ]
8C72.02
Central core disease
[ { "from_icd11": "JA85.Y", "icd10_code": "O358XX0 ", "icd10_title": "" }, { "from_icd11": "JA85.Y", "icd10_code": "O358XX1 ", "icd10_title": "" }, { "from_icd11": "PK98.0", "icd10_code": "Y780", "icd10_title": "Diagnostic and monitoring radiological devices associated with adverse incidents" }, { "from_icd11": "8A80.Z", "icd10_code": "G43B0", "icd10_title": "Ophthalmoplegic migraine, not intractable" }, { "from_icd11": "8A80.Z", "icd10_code": "G43409", "icd10_title": "Hemiplegic migraine, not intractable, without status migrainosus" }, { "from_icd11": "8A80.Z", "icd10_code": "G43A0", "icd10_title": "Cyclical vomiting, in migraine, not intractable" }, { "from_icd11": "8A80.Z", "icd10_code": "G43D0", "icd10_title": "Abdominal migraine, not intractable" }, { "from_icd11": "8A80.Z", "icd10_code": "G43709", "icd10_title": "Chronic migraine without aura, not intractable, without status migrainosus" }, { "from_icd11": "8A80.Z", "icd10_code": "G43A1", "icd10_title": "Cyclical vomiting, in migraine, intractable" }, { "from_icd11": "8A80.Z", "icd10_code": "G43509", "icd10_title": "Persistent migraine aura without cerebral infarction, not intractable, without status migrainosus" }, { "from_icd11": "8A80.Z", "icd10_code": "G43719", "icd10_title": "Chronic migraine without aura, intractable, without status migrainosus" }, { "from_icd11": "8A80.Z", "icd10_code": "G43501", "icd10_title": "Persistent migraine aura without cerebral infarction, not intractable, with status migrainosus" }, { "from_icd11": "8A80.Z", "icd10_code": "G43C0", "icd10_title": "Periodic headache syndromes in child or adult, not intractable" }, { "from_icd11": "8A80.Z", "icd10_code": "G43401", "icd10_title": "Hemiplegic migraine, not intractable, with status migrainosus" }, { "from_icd11": "8A80.Z", "icd10_code": "G43419", "icd10_title": "Hemiplegic migraine, intractable, without status migrainosus" } ]
O358XX0
There is often difficulty confirming the origin of these left atrial densities. Our case highlights the mimicry of cardiac thrombi in clinical presentation and appearance to a myxoid mass seen on an echocardiogram. The left atrium is the most common site of intra-atrial thrombus formation due to the anatomy of the left atrial appendage providing a blood stasis environment . If the thrombus has well-defined borders with a stalk attached to the atrial septal wall, similar to our case, it may further increase suspicion of an atrial myxoma . Although the management of an atrial mass should be based on the clinical situation (accompanying heart disease, etc.) and the echocardiography findings (well-limited mass, echogenicity, etc.), the distinction between myxomas and thrombi may pose considerable diagnostic challenges . An intracardiac thrombus commonly presents as a mass in the left atrial appendage and may be associated with atrial fibrillation, atrial enlargement, mitral stenosis, or tricuspid stenosis . With this presentation, the next step in management is anticoagulation to prevent these thrombi from causing ischemic complications when embolized. In some cases, surgical intervention is needed to remove the mass and obtain a biopsy of the collected sample to confirm the thrombolytic nature versus a myxoma. But atrial thrombi misdiagnosed as myxomas can lead to an unnecessary surgical resection .
4.183594
0.856934
sec[2]/p[1]
en
0.999995
33425523
https://doi.org/10.7759/cureus.11944
[ "atrial", "thrombi", "thrombus", "these", "appendage", "well", "myxoma", "myxomas", "stenosis", "often" ]
[ { "code": "BC46&XA91S4", "title": "Atrial thrombosis" }, { "code": "LA8Z", "title": "Structural developmental anomaly of heart or great vessels, unspecified" }, { "code": "BC40.Z", "title": "Acquired atrial abnormality, unspecified" }, { "code": "BC81.2Z", "title": "Macro reentrant atrial tachycardia, unspecified" }, { "code": "LA8Y", "title": "Other specified structural developmental anomaly of heart or great vessels" }, { "code": "3B65&XT5R", "title": "Acute intravascular thrombotic microangiopathy" }, { "code": "3B65&XT8W", "title": "Chronic intravascular thrombotic microangiopathy" }, { "code": "BA41.Z", "title": "Acute myocardial infarction, unspecified" }, { "code": "PL12.3", "title": "Obstruction of device, as mode of injury or harm" }, { "code": "BD5Y", "title": "Other specified diseases of arteries or arterioles" } ]
=== ICD-11 CODES FOUND === [LA8Z] Structural developmental anomaly of heart or great vessels, unspecified Also known as: Structural developmental anomaly of heart or great vessels, unspecified | Heart malformations | Cardiac malformations | congenital anomaly of heart | congenital heart disease [BC40.Z] Acquired atrial abnormality, unspecified Also known as: Acquired atrial abnormality, unspecified | Acquired atrial abnormality [BC81.2Z] Macro reentrant atrial tachycardia, unspecified Also known as: Macro reentrant atrial tachycardia, unspecified | Macro reentrant atrial tachycardia | MRAT - [macro re-entrant atrial tachycardia] | intra-atrial re-entry tachycardia | Atrial flutter NOS [LA8Y] Other specified structural developmental anomaly of heart or great vessels Also known as: Other specified structural developmental anomaly of heart or great vessels | Congenital anomaly of position or spatial relationships of thoraco-abdominal organs | Usual atrial arrangement | atrial situs solitus | Abnormal atrial arrangement [BA41.Z] Acute myocardial infarction, unspecified Also known as: Acute myocardial infarction, unspecified | Acute myocardial infarction | cardiac attack | heart attack | acute cardiac infarction [PL12.3] Obstruction of device, as mode of injury or harm Definition: Obstruction associated with prosthetic devices, grafts or implants Also known as: Obstruction of device, as mode of injury or harm | occlusion shunt | blockage of device causing obstruction as mode of injury | blocked tube causing obstruction as mode of injury | occlusion of device causing obstruction as mode of injury Excludes: Obstruction of device without injury or harm [BD5Y] Other specified diseases of arteries or arterioles Also known as: Other specified diseases of arteries or arterioles | Arterial or microvascular embolism classified by source | Cardiac embolism | heart embolism | Thrombotic cardiac embolism === GRAPH WALKS === --- Walk 1 --- [LA8Z] Structural developmental anomaly of heart or great vessels, unspecified --PARENT--> [?] Structural developmental anomaly of heart or great vessels Def: A congenital malformation of the heart and/or great vessels or an acquired abnormality unique to the congenitally malformed heart.... --CHILD--> [LA82] Total mirror imagery Def: A congenital malformation in which there is complete mirror-imaged arrangement of the internal organs along the left-right axis of the body.... --- Walk 2 --- [LA8Z] Structural developmental anomaly of heart or great vessels, unspecified --PARENT--> [?] Structural developmental anomaly of heart or great vessels Def: A congenital malformation of the heart and/or great vessels or an acquired abnormality unique to the congenitally malformed heart.... --RELATED_TO--> [?] Congenital cardiac tumor, not otherwise specified Def: A congenital malformation consisting of growth of abnormal tissue within the heart.... --- Walk 3 --- [BC40.Z] Acquired atrial abnormality, unspecified --PARENT--> [BC40] Acquired atrial abnormality Def: A postnatal pathological change in form or function of one or both atriums.... --PARENT--> [?] Diseases of the myocardium or cardiac chambers Def: This refers to diseases of a type of involuntary striated muscle found in the walls and histological foundation of the heart, with specific reference to the atrial and ventricular chambers, as well as... --- Walk 4 --- [BC40.Z] Acquired atrial abnormality, unspecified --PARENT--> [BC40] Acquired atrial abnormality Def: A postnatal pathological change in form or function of one or both atriums.... --CHILD--> [BC40.0] Acquired interatrial communication Def: A postnatal pathological hole or pathway between the atrial chambers.... --- Walk 5 --- [BC81.2Z] Macro reentrant atrial tachycardia, unspecified --PARENT--> [BC81.2] Macro reentrant atrial tachycardia Def: An atrial arrhythmia in which there is intra-atrial reentry or circus movement around a fixed or functional central obstacle. The central obstacle may consist of normal (e.g. valves) or abnormal (e.g.... --CHILD--> [BC81.20] Cavotricuspid isthmus dependent macroreentry tachycardia Def: A macro re-entrant atrial tachycardia that rotates around the tricuspid annulus.... --- Walk 6 --- [BC81.2Z] Macro reentrant atrial tachycardia, unspecified --PARENT--> [BC81.2] Macro reentrant atrial tachycardia Def: An atrial arrhythmia in which there is intra-atrial reentry or circus movement around a fixed or functional central obstacle. The central obstacle may consist of normal (e.g. valves) or abnormal (e.g.... --CHILD--> [BC81.21] Non-scar, non-isthmus dependent macro reentrant atrial tachycardia Def: A macro re-entrant atrial tachycardia coursing around a normal cardiac structure (except the cavotricuspid isthmus) such as the mitral valve annulus, or superior caval vein....
[ "[LA8Z] Structural developmental anomaly of heart or great vessels, unspecified\n --PARENT--> [?] Structural developmental anomaly of heart or great vessels\n Def: A congenital malformation of the heart and/or great vessels or an acquired abnormality unique to the congenitally malformed heart....\n --CHILD--> [LA82] Total mirror imagery\n Def: A congenital malformation in which there is complete mirror-imaged arrangement of the internal organs along the left-right axis of the body....", "[LA8Z] Structural developmental anomaly of heart or great vessels, unspecified\n --PARENT--> [?] Structural developmental anomaly of heart or great vessels\n Def: A congenital malformation of the heart and/or great vessels or an acquired abnormality unique to the congenitally malformed heart....\n --RELATED_TO--> [?] Congenital cardiac tumor, not otherwise specified\n Def: A congenital malformation consisting of growth of abnormal tissue within the heart....", "[BC40.Z] Acquired atrial abnormality, unspecified\n --PARENT--> [BC40] Acquired atrial abnormality\n Def: A postnatal pathological change in form or function of one or both atriums....\n --PARENT--> [?] Diseases of the myocardium or cardiac chambers\n Def: This refers to diseases of a type of involuntary striated muscle found in the walls and histological foundation of the heart, with specific reference to the atrial and ventricular chambers, as well as...", "[BC40.Z] Acquired atrial abnormality, unspecified\n --PARENT--> [BC40] Acquired atrial abnormality\n Def: A postnatal pathological change in form or function of one or both atriums....\n --CHILD--> [BC40.0] Acquired interatrial communication\n Def: A postnatal pathological hole or pathway between the atrial chambers....", "[BC81.2Z] Macro reentrant atrial tachycardia, unspecified\n --PARENT--> [BC81.2] Macro reentrant atrial tachycardia\n Def: An atrial arrhythmia in which there is intra-atrial reentry or circus movement around a fixed or functional central obstacle. The central obstacle may consist of normal (e.g. valves) or abnormal (e.g....\n --CHILD--> [BC81.20] Cavotricuspid isthmus dependent macroreentry tachycardia\n Def: A macro re-entrant atrial tachycardia that rotates around the tricuspid annulus....", "[BC81.2Z] Macro reentrant atrial tachycardia, unspecified\n --PARENT--> [BC81.2] Macro reentrant atrial tachycardia\n Def: An atrial arrhythmia in which there is intra-atrial reentry or circus movement around a fixed or functional central obstacle. The central obstacle may consist of normal (e.g. valves) or abnormal (e.g....\n --CHILD--> [BC81.21] Non-scar, non-isthmus dependent macro reentrant atrial tachycardia\n Def: A macro re-entrant atrial tachycardia coursing around a normal cardiac structure (except the cavotricuspid isthmus) such as the mitral valve annulus, or superior caval vein...." ]
BC46&XA91S4
Atrial thrombosis
[ { "from_icd11": "LA8Z", "icd10_code": "Q248", "icd10_title": "Other specified congenital malformations of heart" }, { "from_icd11": "LA8Z", "icd10_code": "Q893", "icd10_title": "Situs inversus" }, { "from_icd11": "LA8Z", "icd10_code": "Q212", "icd10_title": "Atrioventricular septal defect" }, { "from_icd11": "LA8Z", "icd10_code": "Q249", "icd10_title": "Congenital malformation of heart, unspecified" }, { "from_icd11": "LA8Z", "icd10_code": "Q246", "icd10_title": "Congenital heart block" }, { "from_icd11": "LA8Z", "icd10_code": "Q242", "icd10_title": "Cor triatriatum" }, { "from_icd11": "LA8Z", "icd10_code": "Q219", "icd10_title": "Congenital malformation of cardiac septum, unspecified" }, { "from_icd11": "LA8Z", "icd10_code": "Q208", "icd10_title": "Other congenital malformations of cardiac chambers and connections" }, { "from_icd11": "LA8Z", "icd10_code": "Q897", "icd10_title": "Multiple congenital malformations, not elsewhere classified" }, { "from_icd11": "LA8Z", "icd10_code": "Q209", "icd10_title": "Congenital malformation of cardiac chambers and connections, unspecified" }, { "from_icd11": "LA8Z", "icd10_code": "Q218", "icd10_title": "Other congenital malformations of cardiac septa" }, { "from_icd11": "LA8Z", "icd10_code": "Q20", "icd10_title": "Congenital malformations of cardiac chambers and connections" }, { "from_icd11": "LA8Z", "icd10_code": "Q206", "icd10_title": "Isomerism of atrial appendages" }, { "from_icd11": "LA8Z", "icd10_code": "Q21", "icd10_title": "Congenital malformations of cardiac septa" }, { "from_icd11": "LA8Z", "icd10_code": "Q226", "icd10_title": "Hypoplastic right heart syndrome" } ]
Q248
Other specified congenital malformations of heart
A four-year-old female presented to King Abdullah Specialist Children’s Hospital Emergency Department with a history of recurrent fevers, productive cough, and a headache for the past two weeks. This patient has a significant past medical history of IL12RB1 deficiency, disseminated BCGitis, and disseminated salmonellosis, with a history of multiple pediatric intensive care unit admissions, secondary to septic shock. She was born to consanguineous parents, and her older sister was also diagnosed with IL12RB1 deficiency. On examination, she was alert, interactive, and not in pain or respiratory distress. The patient had generalized urticarial macules and papules with a few scattered purpuric lesions . There were multiple enlarged left cervical lymph nodes and an enlarged left inguinal lymph node, measuring 3x4 cm, with erythema of overlying skin. Chest, cardiovascular, and abdominal examinations were unremarkable. Height and weight growth parameters were normal. Laboratory investigations revealed a hemoglobin level of 59 gm/L. Low blood sodium levels for age-adjusted values were noted, as shown in Table 1 . C-reactive protein was 92 mg/L. Coagulation studies, liver panel, creatinine, and blood urea nitrogen all fell within the normal range. COVID-19 swab and blood cultures were taken. Thereafter, the patient was admitted for observation and transfused with 5 mL/kg of packed red blood cells (PRBCs).
3.830078
0.985352
sec[1]/p[0]
en
0.999996
PMC8855683
https://doi.org/10.7759/cureus.21415
[ "blood", "past", "deficiency", "disseminated", "multiple", "enlarged", "lymph", "four", "king", "abdullah" ]
[ { "code": "3C0Z", "title": "Diseases of the blood or blood-forming organs, unspecified" }, { "code": "MF50.4Z", "title": "Haematuria, unspecified" }, { "code": "MA12.1", "title": "Finding of cocaine in blood" }, { "code": "MA12.4", "title": "Finding of steroid agent in blood" }, { "code": "MA12.2", "title": "Finding of hallucinogen in blood" }, { "code": "PL13.8", "title": "Expired or deteriorated medication or substance, as mode of injury or harm" }, { "code": "BA50", "title": "Old myocardial infarction" }, { "code": "8B25.4", "title": "Late effects of stroke not known if ischaemic or haemorrhagic" }, { "code": "QE51.1", "title": "History of spouse or partner violence" }, { "code": "PB36", "title": "Unintentional exposure to or harmful effects of other or unspecified substances chiefly nonmedicinal as to source" } ]
=== ICD-11 CODES FOUND === [3C0Z] Diseases of the blood or blood-forming organs, unspecified Also known as: Diseases of the blood or blood-forming organs, unspecified | Blood, lymph or spleen disease | blood condition NOS | blood disorder NOS | bone marrow disease NOS [MF50.4Z] Haematuria, unspecified Also known as: Haematuria, unspecified | Haematuria | blood in urine | urinary blood | haematuria NOS [MA12.1] Finding of cocaine in blood Also known as: Finding of cocaine in blood | cocaine in blood [MA12.4] Finding of steroid agent in blood Also known as: Finding of steroid agent in blood | steroid in blood [MA12.2] Finding of hallucinogen in blood Also known as: Finding of hallucinogen in blood | hallucinogen in blood [PL13.8] Expired or deteriorated medication or substance, as mode of injury or harm Also known as: Expired or deteriorated medication or substance, as mode of injury or harm | drug past expiry date | expired drug | deteriorated drug | drug past due date [BA50] Old myocardial infarction Definition: Past myocardial infarction diagnosed by electrocardiogram (ECG) or other special investigation, but currently presenting no symptoms. Also known as: Old myocardial infarction | past myocardial infarction | healed myocardial infarction | myocardial scar | myocardial scarring Includes: healed myocardial infarction [8B25.4] Late effects of stroke not known if ischaemic or haemorrhagic Definition: Late effects occurring 1 month or later after the onset of the disease. Codes for acute stroke should be exclusively used for the acute stroke and immediately related hospitalisation episodes. Also known as: Late effects of stroke not known if ischaemic or haemorrhagic | sequelae of stroke, not specified as haemorrhage or infarction | old cerebrovascular accident | old CVA - [cerebrovascular accident] | old stroke [QE51.1] History of spouse or partner violence Definition: Non-accidental acts of physical force, forced or coerced sexual acts, verbal or symbolic acts, or significant caregiving omissions that result in harm to a spouse or intimate partner or that have a reasonable potential for harm. Also known as: History of spouse or partner violence | spouse violence | partner violence | History of spouse or partner violence, physical | partner physical violence [PB36] Unintentional exposure to or harmful effects of other or unspecified substances chiefly nonmedicinal as to source Also known as: Unintentional exposure to or harmful effects of other or unspecified substances chiefly nonmedicinal as to source | Unintentional exposure to or harmful effects of other or unspecified gases, fumes or vapours | Unintentional exposure to or harmful effects of nitrogen oxides | Unintentional exposure to or harmful effects of sulfur dioxide | Unintentional exposure to or harmful effects of formaldehyde === GRAPH WALKS === --- Walk 1 --- [3C0Z] Diseases of the blood or blood-forming organs, unspecified --PARENT--> [03] Diseases of the blood or blood-forming organs Def: This chapter includes diseases of the blood as well as diseases of blood forming organs.... --EXCLUDES--> [?] Diseases of the immune system --- Walk 2 --- [3C0Z] Diseases of the blood or blood-forming organs, unspecified --PARENT--> [03] Diseases of the blood or blood-forming organs Def: This chapter includes diseases of the blood as well as diseases of blood forming organs.... --CHILD--> [?] Diseases of spleen --- Walk 3 --- [MF50.4Z] Haematuria, unspecified --PARENT--> [MF50.4] Haematuria Def: Hematuria means presence of blood or red blood cells (RBCs) in the urine. There are two types of hematuria: gross hematuria (when one can see the blood in the urine) and microscopic hematuria (when th... --CHILD--> [MF50.41] Microscopic haematuria --- Walk 4 --- [MF50.4Z] Haematuria, unspecified --PARENT--> [MF50.4] Haematuria Def: Hematuria means presence of blood or red blood cells (RBCs) in the urine. There are two types of hematuria: gross hematuria (when one can see the blood in the urine) and microscopic hematuria (when th... --EXCLUDES--> [?] Recurrent or persistent glomerular haematuria Def: The presence in the urine of glomerular origin red blood cells (RBCs). In microscopic haematuria the urine appears normal to the naked eye, but examination with a microscope shows a high number of RBC... --- Walk 5 --- [MA12.1] Finding of cocaine in blood --PARENT--> [MA12] Clinical findings of drugs, medicaments and biological substances in blood, blood-forming organs, or the immune system --PARENT--> [?] Clinical findings in blood, blood-forming organs, or the immune system --- Walk 6 --- [MA12.1] Finding of cocaine in blood --PARENT--> [MA12] Clinical findings of drugs, medicaments and biological substances in blood, blood-forming organs, or the immune system --PARENT--> [?] Clinical findings in blood, blood-forming organs, or the immune system
[ "[3C0Z] Diseases of the blood or blood-forming organs, unspecified\n --PARENT--> [03] Diseases of the blood or blood-forming organs\n Def: This chapter includes diseases of the blood as well as diseases of blood forming organs....\n --EXCLUDES--> [?] Diseases of the immune system", "[3C0Z] Diseases of the blood or blood-forming organs, unspecified\n --PARENT--> [03] Diseases of the blood or blood-forming organs\n Def: This chapter includes diseases of the blood as well as diseases of blood forming organs....\n --CHILD--> [?] Diseases of spleen", "[MF50.4Z] Haematuria, unspecified\n --PARENT--> [MF50.4] Haematuria\n Def: Hematuria means presence of blood or red blood cells (RBCs) in the urine. There are two types of hematuria: gross hematuria (when one can see the blood in the urine) and microscopic hematuria (when th...\n --CHILD--> [MF50.41] Microscopic haematuria", "[MF50.4Z] Haematuria, unspecified\n --PARENT--> [MF50.4] Haematuria\n Def: Hematuria means presence of blood or red blood cells (RBCs) in the urine. There are two types of hematuria: gross hematuria (when one can see the blood in the urine) and microscopic hematuria (when th...\n --EXCLUDES--> [?] Recurrent or persistent glomerular haematuria\n Def: The presence in the urine of glomerular origin red blood cells (RBCs). In microscopic haematuria the urine appears normal to the naked eye, but examination with a microscope shows a high number of RBC...", "[MA12.1] Finding of cocaine in blood\n --PARENT--> [MA12] Clinical findings of drugs, medicaments and biological substances in blood, blood-forming organs, or the immune system\n --PARENT--> [?] Clinical findings in blood, blood-forming organs, or the immune system", "[MA12.1] Finding of cocaine in blood\n --PARENT--> [MA12] Clinical findings of drugs, medicaments and biological substances in blood, blood-forming organs, or the immune system\n --PARENT--> [?] Clinical findings in blood, blood-forming organs, or the immune system" ]
3C0Z
Diseases of the blood or blood-forming organs, unspecified
[ { "from_icd11": "3C0Z", "icd10_code": "D75A", "icd10_title": "Glucose-6-phosphate dehydrogenase (G6PD) deficiency without anemia" }, { "from_icd11": "3C0Z", "icd10_code": "D7581", "icd10_title": "Myelofibrosis" }, { "from_icd11": "3C0Z", "icd10_code": "D7582", "icd10_title": "Heparin induced thrombocytopenia (HIT)" }, { "from_icd11": "3C0Z", "icd10_code": "D7589", "icd10_title": "Other specified diseases of blood and blood-forming organs" }, { "from_icd11": "3C0Z", "icd10_code": "D759", "icd10_title": "Disease of blood and blood-forming organs, unspecified" }, { "from_icd11": "3C0Z", "icd10_code": "D763", "icd10_title": "Other histiocytosis syndromes" }, { "from_icd11": "3C0Z", "icd10_code": "Q899", "icd10_title": "Congenital malformation, unspecified" }, { "from_icd11": "3C0Z", "icd10_code": "III", "icd10_title": "" }, { "from_icd11": "3C0Z", "icd10_code": "D70-D77", "icd10_title": "" }, { "from_icd11": "3C0Z", "icd10_code": "D75", "icd10_title": "Other and unspecified diseases of blood and blood-forming organs" }, { "from_icd11": "3C0Z", "icd10_code": "D77", "icd10_title": "Other disorders of blood and blood-forming organs in diseases classified elsewhere" }, { "from_icd11": "3C0Z", "icd10_code": "D758", "icd10_title": "Other specified diseases of blood and blood-forming organs" }, { "from_icd11": "3C0Z", "icd10_code": "D76", "icd10_title": "Other specified diseases with participation of lymphoreticular and reticulohistiocytic tissue" }, { "from_icd11": "MF50.4Z", "icd10_code": "R310", "icd10_title": "Gross hematuria" }, { "from_icd11": "MF50.4Z", "icd10_code": "R312", "icd10_title": "Other microscopic hematuria" } ]
D75A
Glucose-6-phosphate dehydrogenase (G6PD) deficiency without anemia
During clinical follow-up, a progressively more elongated face and a more pronounced nasal bridge were noticed . At the last examination (12 years and 6 months), his height was 163.5 cm (>97th percentile), weight was 45 kg (75th−90th percentile), and head circumference was 54 cm (50th−75th percentile). He had a hypomimic and asymmetric face, flat occiput, hypertelorism, periorbital fullness, bilateral ptosis (more pronounced on the left side), epicanthus, exotropia, thick alae nasi, microretrognathia, a thin upper lip, a high-arched palate, small and spaced teeth, poor representation of muscle mass, pectus excavatum, scoliosis, widening of the proximal interphalangeal joints of the hands, flat feet with sandal gap, and II-III toe partial cutaneous syndactyly. He also showed vascular anomalies: visible vessels on the lower eyelids and congenital vascular anomalies (flat angiomas) that disappeared upon pressure, some in the occiput and vertex, and multiple in the back . Abdominal ultrasound, audiometric testing, fundus examination, and electroneurography (ENG) were normal. A small aneurysm at the level of the interatrial septum was detected during the echocardiography. Brain MRI at 6 years revealed cysts of the septum pellucidum and of the cavum vergae . A brain CT scan performed at 3 years of age revealed right choanal atresia . The ophthalmological evaluation documented hyperopia and astigmatism.
3.919922
0.981445
sec[1]/sec[1]/p[0]
en
0.999995
PMC10382204
https://doi.org/10.3389/fneur.2023.1207176
[ "percentile", "flat", "face", "pronounced", "occiput", "small", "vascular", "anomalies", "septum", "brain" ]
[ { "code": "5B81.00", "title": "Obesity in children or adolescents" }, { "code": "MB24.62", "title": "Flat affect" }, { "code": "FA31.5", "title": "Acquired pes planus" }, { "code": "1E81", "title": "Plane warts" }, { "code": "FA70.0", "title": "Kyphosis" }, { "code": "LA11.1", "title": "Structural developmental anomalies of cornea" }, { "code": "ED90.1", "title": "Periorificial dermatitis" }, { "code": "8B88.0", "title": "Bell palsy" }, { "code": "LA51", "title": "Facial clefts" }, { "code": "8B88.Z", "title": "Disorders of facial nerve, unspecified" } ]
=== ICD-11 CODES FOUND === [5B81.00] Obesity in children or adolescents Definition: In infants, children and adolescents, BMI categories for defining obesity vary by age and gender based on WHO growth charts. Children 0 to 5 years have obesity if weight-for-length/height or BMI-for-age is above 3 standard deviations of the median of the WHO Child Growth Standards. Children aged 5 to 19 years have obesity if BMI-for-age is above 2 standard deviations of the median of WHO Growth Reference for School-aged Children and Adolescents. Also known as: Obesity in children or adolescents | morbid obesity in children or adolescents | BMI-for age -[body mass index-for-age] percentile greater than 95 percent | Obesity in infants or children up to 5 years of age | Obesity in school-aged children or adolescents from 5 to 19 years [MB24.62] Flat affect Definition: Absence or near absence of any sign of affective expression. Also known as: Flat affect [FA31.5] Acquired pes planus Also known as: Acquired pes planus | acquired flat foot | acquired talipes planus | fallen arch | flat foot Excludes: Congenital pes planus [1E81] Plane warts Definition: Plane warts (flat warts) are clinically distinct from common warts and manifest as multiple small flat-topped, often lightly pigmented papules on the face or extremities. They are caused by human papillomavirus (HPV) subtypes 3 and 10. Also known as: Plane warts | Verruca plana | Flat warts [FA70.0] Kyphosis Definition: This is a curving of the spine that causes a bowing or rounding of the back, which leads to a hunchback or slouching posture. Also known as: Kyphosis | postural kyphosis | Kyphosis with no determinant | primary kyphosis | idiopathic kyphosis Excludes: Post radiation kyphosis [LA11.1] Structural developmental anomalies of cornea Definition: Any condition caused by failure of the cornea to correctly develop during the antenatal period. Also known as: Structural developmental anomalies of cornea | Malformations of cornea | Cornea plana | Flat cornea | Cornea plana, unilateral [ED90.1] Periorificial dermatitis Definition: Periorificial dermatitis is a term which links two erythematous and papulopustular facial dermatoses that are strongly linked to prolonged potent topical corticosteroid use, namely perioral dermatitis and periocular dermatitis. It is characterised by the development of erythema, papules and pustules in perioral and periocular skin. Also known as: Periorificial dermatitis | Perioral dermatitis | Corticosteroid-induced perioral dermatitis | Periocular dermatitis | Periorificial dermatitis of eyelids [8B88.0] Bell palsy Also known as: Bell palsy | Facial nerve paralysis | Facial nerve palsy | Seventh cranial nerve paralysis | facial palsy [LA51] Facial clefts Definition: Any condition caused by failure of the structures of the face to correctly develop during the antenatal period. These conditions are characterised by a partition in bone, soft tissue, or skin of the face. Also known as: Facial clefts | Craniofacial clefts | Median facial cleft | Tessier number 0-14 and 30 facial cleft | Midline facial cleft Excludes: Frontofacionasal dysostosis | Frontonasal dysplasia [8B88.Z] Disorders of facial nerve, unspecified Also known as: Disorders of facial nerve, unspecified | Disorders of facial nerve | Neuropathy of facial nerve | Disorders of 7th cranial nerve | Disorders of the seventh cranial nerve === GRAPH WALKS === --- Walk 1 --- [5B81.00] Obesity in children or adolescents Def: In infants, children and adolescents, BMI categories for defining obesity vary by age and gender based on WHO growth charts. Children 0 to 5 years have obesity if weight-for-length/height or BMI-for-a... --PARENT--> [5B81.0] Obesity due to energy imbalance Def: Obesity is a chronic complex disease defined by excessive adiposity that can impair health. It is in most cases a multifactorial disease due to obesogenic environments, psycho-social factors and genet... --CHILD--> [5B81.00] Obesity in children or adolescents Def: In infants, children and adolescents, BMI categories for defining obesity vary by age and gender based on WHO growth charts. Children 0 to 5 years have obesity if weight-for-length/height or BMI-for-a... --- Walk 2 --- [5B81.00] Obesity in children or adolescents Def: In infants, children and adolescents, BMI categories for defining obesity vary by age and gender based on WHO growth charts. Children 0 to 5 years have obesity if weight-for-length/height or BMI-for-a... --PARENT--> [5B81.0] Obesity due to energy imbalance Def: Obesity is a chronic complex disease defined by excessive adiposity that can impair health. It is in most cases a multifactorial disease due to obesogenic environments, psycho-social factors and genet... --PARENT--> [5B81] Obesity Def: Obesity is a chronic complex disease defined by excessive adiposity that can impair health. It is in most cases a multifactorial disease due to obesogenic environments, psycho-social factors and genet... --- Walk 3 --- [MB24.62] Flat affect Def: Absence or near absence of any sign of affective expression.... --PARENT--> [MB24.6] Disturbance of affect Def: A disturbance in the expression or outward manifestation of mood.... --CHILD--> [MB24.61] Blunted affect Def: A severe reduction in the expressive range and intensity of affect, but less than is observed in Flat affect.... --- Walk 4 --- [MB24.62] Flat affect Def: Absence or near absence of any sign of affective expression.... --PARENT--> [MB24.6] Disturbance of affect Def: A disturbance in the expression or outward manifestation of mood.... --CHILD--> [MB24.62] Flat affect Def: Absence or near absence of any sign of affective expression.... --- Walk 5 --- [FA31.5] Acquired pes planus --EXCLUDES--> [?] Congenital pes planus Def: Any condition caused by failure of the foot to correctly develop during the antenatal period. These conditions are characterised by severe rigid flat foot deformity.... --CHILD--> [?] Congenital pes planus, unilateral --- Walk 6 --- [FA31.5] Acquired pes planus --EXCLUDES--> [?] Congenital pes planus Def: Any condition caused by failure of the foot to correctly develop during the antenatal period. These conditions are characterised by severe rigid flat foot deformity.... --CHILD--> [?] Congenital pes planus, unilateral
[ "[5B81.00] Obesity in children or adolescents\n Def: In infants, children and adolescents, BMI categories for defining obesity vary by age and gender based on WHO growth charts. Children 0 to 5 years have obesity if weight-for-length/height or BMI-for-a...\n --PARENT--> [5B81.0] Obesity due to energy imbalance\n Def: Obesity is a chronic complex disease defined by excessive adiposity that can impair health. It is in most cases a multifactorial disease due to obesogenic environments, psycho-social factors and genet...\n --CHILD--> [5B81.00] Obesity in children or adolescents\n Def: In infants, children and adolescents, BMI categories for defining obesity vary by age and gender based on WHO growth charts. Children 0 to 5 years have obesity if weight-for-length/height or BMI-for-a...", "[5B81.00] Obesity in children or adolescents\n Def: In infants, children and adolescents, BMI categories for defining obesity vary by age and gender based on WHO growth charts. Children 0 to 5 years have obesity if weight-for-length/height or BMI-for-a...\n --PARENT--> [5B81.0] Obesity due to energy imbalance\n Def: Obesity is a chronic complex disease defined by excessive adiposity that can impair health. It is in most cases a multifactorial disease due to obesogenic environments, psycho-social factors and genet...\n --PARENT--> [5B81] Obesity\n Def: Obesity is a chronic complex disease defined by excessive adiposity that can impair health. It is in most cases a multifactorial disease due to obesogenic environments, psycho-social factors and genet...", "[MB24.62] Flat affect\n Def: Absence or near absence of any sign of affective expression....\n --PARENT--> [MB24.6] Disturbance of affect\n Def: A disturbance in the expression or outward manifestation of mood....\n --CHILD--> [MB24.61] Blunted affect\n Def: A severe reduction in the expressive range and intensity of affect, but less than is observed in Flat affect....", "[MB24.62] Flat affect\n Def: Absence or near absence of any sign of affective expression....\n --PARENT--> [MB24.6] Disturbance of affect\n Def: A disturbance in the expression or outward manifestation of mood....\n --CHILD--> [MB24.62] Flat affect\n Def: Absence or near absence of any sign of affective expression....", "[FA31.5] Acquired pes planus\n --EXCLUDES--> [?] Congenital pes planus\n Def: Any condition caused by failure of the foot to correctly develop during the antenatal period. These conditions are characterised by severe rigid flat foot deformity....\n --CHILD--> [?] Congenital pes planus, unilateral", "[FA31.5] Acquired pes planus\n --EXCLUDES--> [?] Congenital pes planus\n Def: Any condition caused by failure of the foot to correctly develop during the antenatal period. These conditions are characterised by severe rigid flat foot deformity....\n --CHILD--> [?] Congenital pes planus, unilateral" ]
5B81.00
Obesity in children or adolescents
[ { "from_icd11": "FA31.5", "icd10_code": "M2141", "icd10_title": "Flat foot [pes planus] (acquired), right foot" }, { "from_icd11": "FA31.5", "icd10_code": "M2142", "icd10_title": "Flat foot [pes planus] (acquired), left foot" }, { "from_icd11": "FA31.5", "icd10_code": "M2140", "icd10_title": "Flat foot [pes planus] (acquired), unspecified foot" }, { "from_icd11": "FA31.5", "icd10_code": "M214", "icd10_title": "Flat foot [pes planus] (acquired)" }, { "from_icd11": "1E81", "icd10_code": "B078", "icd10_title": "Other viral warts" }, { "from_icd11": "1E81", "icd10_code": "B070", "icd10_title": "Plantar wart" }, { "from_icd11": "1E81", "icd10_code": "B079", "icd10_title": "Viral wart, unspecified" }, { "from_icd11": "1E81", "icd10_code": "B07", "icd10_title": "Viral warts" }, { "from_icd11": "FA70.0", "icd10_code": "M40209", "icd10_title": "Unspecified kyphosis, site unspecified" }, { "from_icd11": "FA70.0", "icd10_code": "M4014", "icd10_title": "Other secondary kyphosis, thoracic region" }, { "from_icd11": "FA70.0", "icd10_code": "M40204", "icd10_title": "Unspecified kyphosis, thoracic region" }, { "from_icd11": "FA70.0", "icd10_code": "M40202", "icd10_title": "Unspecified kyphosis, cervical region" }, { "from_icd11": "FA70.0", "icd10_code": "M40294", "icd10_title": "Other kyphosis, thoracic region" }, { "from_icd11": "FA70.0", "icd10_code": "M40299", "icd10_title": "Other kyphosis, site unspecified" }, { "from_icd11": "FA70.0", "icd10_code": "M40295", "icd10_title": "Other kyphosis, thoracolumbar region" } ]
M2141
Flat foot [pes planus] (acquired), right foot
In our case, the primary cause of PVA was unknown. Pregnancy and the post-partum period are prothrombotic states for a number of reasons and are associated with a four- to fivefold increased risk of VTE compared to non-pregnant women . The physiologic and anatomical changes responsible for this increased risk include increased production of factors V, VII, VIII, IX, X, and XII, von Willebrand factor, fibrinogen, decreased protein S activity, decreased fibrinolysis, and progesterone-mediated veno-dilation, increased blood volume and venous hypertension. Anatomically, compression of the inferior vena cava and pelvic veins as the uterus enlarges contributes to venous dilation, hypertension, and stasis . Increased venodilation and blood volume have been shown to result in an increase in diameter of lower extremity vasculature, including the PV . It could therefore be hypothesized that pregnancy may have played a role in causing and/or contributing to the formation and growth of the PVA, as well as promoting intra-aneurysmal thrombus formation. A similar explanation has been proposed in a patient who presented with pain in the posterior fossa post-partum with a history of a popliteal mass identified in her second trimester who was found to have a dissecting PVA . The recurrence of PE in the post-partum period in our case reinforces this as a high-risk period, which extends up to 12 weeks post-partum .
4.230469
0.540527
sec[2]/p[1]
en
0.999998
PMC10161411
https://doi.org/10.1186/s12959-023-00495-2
[ "partum", "period", "risk", "pregnancy", "this", "dilation", "blood", "venous", "hypertension", "formation" ]
[ { "code": "4A60.0", "title": "Familial Mediterranean fever" }, { "code": "GA20.3", "title": "Abnormal regularity of uterine bleeding" }, { "code": "8C74.1Z", "title": "Periodic paralysis, unspecified" }, { "code": "MD11.Y", "title": "Other specified abnormalities of breathing" }, { "code": "GA20.50", "title": "Heavy menstrual bleeding" }, { "code": "QC4Y", "title": "Personal history of other specified health problems" }, { "code": "QA43.Z", "title": "Supervision of high-risk pregnancy, unspecified" }, { "code": "QA43.Y", "title": "Other specified supervision of high-risk pregnancy" }, { "code": "QD84.Z", "title": "Occupational exposure to risk-factors, unspecified" }, { "code": "MB26.A", "title": "Suicidal ideation" } ]
=== ICD-11 CODES FOUND === [4A60.0] Familial Mediterranean fever Definition: FMF is an autoinflammatory disease associated with mutations in pyrin resulting in enhanced IL1 beta production. This results in clinical attacks of inflammation in the form of fever and serositis in the form of peritoneal, pleural or synovial inflammation along with increased acute phase reactants. Also known as: Familial Mediterranean fever | Periodic disease | FMF - [familial mediterranean fever] | periodic fever | periodic polyserositis [GA20.3] Abnormal regularity of uterine bleeding Definition: A condition of the genital system affecting females, caused by hormonal disturbances. This condition is characterised by abnormal menstruation, with a between cycle variation of 2-20 days. Also known as: Abnormal regularity of uterine bleeding | Irregular menstrual bleeding | irregular cycle menstruation | irregular menses | irregular menstrual cycle [8C74.1Z] Periodic paralysis, unspecified Also known as: Periodic paralysis, unspecified | Periodic paralysis | Westphal disease | periodic myotonia | myoplegic dystrophy [MD11.Y] Other specified abnormalities of breathing Also known as: Other specified abnormalities of breathing | Bradypnoea | Choking sensation | Hypoventilation | hypoventilation syndrome NOS [GA20.50] Heavy menstrual bleeding Definition: Menstruation with heavy (> 80 ml) volume of monthly blood loss Also known as: Heavy menstrual bleeding | menstruation excessive | Heavy menstrual bleeding caused by bleeding disorders | Excessive menstruation with regular cycle | excessive menses [QC4Y] Personal history of other specified health problems Also known as: Personal history of other specified health problems | Personal history of diseases of the circulatory system | history of disease or disorder of circulatory system | personal history of conditions classifiable as diseases of the circulatory system | Personal history of diseases of the respiratory system [QA43.Z] Supervision of high-risk pregnancy, unspecified Also known as: Supervision of high-risk pregnancy, unspecified | Supervision of high-risk pregnancy [QA43.Y] Other specified supervision of high-risk pregnancy Also known as: Other specified supervision of high-risk pregnancy | Supervision of pregnancy with grand multiparity | pregnancy management affected by grand multiparity | multiparity affecting management of pregnancy, labour and delivery | pregnancy supervision for multiparity [QD84.Z] Occupational exposure to risk-factors, unspecified Also known as: Occupational exposure to risk-factors, unspecified | Occupational exposure to risk-factors | problem with occupational physical environment [MB26.A] Suicidal ideation Definition: Thoughts, ideas, or ruminations about the possibility of ending one's life, ranging from thinking that one would be better off dead to formulation of elaborate plans. Also known as: Suicidal ideation | suicidal tendency | suicidal tendencies | suicidal ideation tendencies | suicide risk Excludes: Suicide attempt | Personal history of self-harm === GRAPH WALKS === --- Walk 1 --- [4A60.0] Familial Mediterranean fever Def: FMF is an autoinflammatory disease associated with mutations in pyrin resulting in enhanced IL1 beta production. This results in clinical attacks of inflammation in the form of fever and serositis in ... --PARENT--> [4A60] Monogenic autoinflammatory syndromes Def: Monogenic hereditary autoinflammatory diseases characterised by apparently unprovoked generalised inflammation in the absence of infection or high titre autoantibodies.... --CHILD--> [4A60.1] Cryopyrin-associated periodic syndromes Def: CAPS is an autoinflammatory disease associated with gain of function changes in the cryopyrin protein, resulting in inflammasome activation and enhanced IL1 beta production. This results in clinical s... --- Walk 2 --- [4A60.0] Familial Mediterranean fever Def: FMF is an autoinflammatory disease associated with mutations in pyrin resulting in enhanced IL1 beta production. This results in clinical attacks of inflammation in the form of fever and serositis in ... --PARENT--> [4A60] Monogenic autoinflammatory syndromes Def: Monogenic hereditary autoinflammatory diseases characterised by apparently unprovoked generalised inflammation in the absence of infection or high titre autoantibodies.... --PARENT--> [?] Autoinflammatory disorders --- Walk 3 --- [GA20.3] Abnormal regularity of uterine bleeding Def: A condition of the genital system affecting females, caused by hormonal disturbances. This condition is characterised by abnormal menstruation, with a between cycle variation of 2-20 days.... --PARENT--> [GA20] Menstrual cycle bleeding disorders --CHILD--> [GA20.2] Ovulation bleeding Def: A condition of the genital system affecting females, caused by natural and routine fluctuations in endocrine hormones. This condition is characterised by recurrent and cyclic bleeding of the uterine l... --- Walk 4 --- [GA20.3] Abnormal regularity of uterine bleeding Def: A condition of the genital system affecting females, caused by hormonal disturbances. This condition is characterised by abnormal menstruation, with a between cycle variation of 2-20 days.... --PARENT--> [GA20] Menstrual cycle bleeding disorders --CHILD--> [GA20.1] Abnormal frequency of uterine bleeding Def: Any condition of the genital system affecting females, caused by hormonal disturbances. These conditions are characterised by menstrual bleeding episodes that occur with increased frequency or are del... --- Walk 5 --- [8C74.1Z] Periodic paralysis, unspecified --PARENT--> [8C74.1] Periodic paralysis Def: Rare group of neuromuscular disorders that are associated with defects in ion channels. Characterized by intermittent episodes of severe weakness of the limbs usually after heavy exercise, fasting, or... --CHILD--> [8C74.11] Hyperkalaemic periodic paralysis Def: Hyperkalaemic periodic paralysis (HyperPP) is a muscle disorder characterised by episodic attacks of muscle weakness associated with an increase in serum potassium concentration.... --- Walk 6 --- [8C74.1Z] Periodic paralysis, unspecified --PARENT--> [8C74.1] Periodic paralysis Def: Rare group of neuromuscular disorders that are associated with defects in ion channels. Characterized by intermittent episodes of severe weakness of the limbs usually after heavy exercise, fasting, or... --CHILD--> [8C74.1Y] Other specified periodic paralysis
[ "[4A60.0] Familial Mediterranean fever\n Def: FMF is an autoinflammatory disease associated with mutations in pyrin resulting in enhanced IL1 beta production. This results in clinical attacks of inflammation in the form of fever and serositis in ...\n --PARENT--> [4A60] Monogenic autoinflammatory syndromes\n Def: Monogenic hereditary autoinflammatory diseases characterised by apparently unprovoked generalised inflammation in the absence of infection or high titre autoantibodies....\n --CHILD--> [4A60.1] Cryopyrin-associated periodic syndromes\n Def: CAPS is an autoinflammatory disease associated with gain of function changes in the cryopyrin protein, resulting in inflammasome activation and enhanced IL1 beta production. This results in clinical s...", "[4A60.0] Familial Mediterranean fever\n Def: FMF is an autoinflammatory disease associated with mutations in pyrin resulting in enhanced IL1 beta production. This results in clinical attacks of inflammation in the form of fever and serositis in ...\n --PARENT--> [4A60] Monogenic autoinflammatory syndromes\n Def: Monogenic hereditary autoinflammatory diseases characterised by apparently unprovoked generalised inflammation in the absence of infection or high titre autoantibodies....\n --PARENT--> [?] Autoinflammatory disorders", "[GA20.3] Abnormal regularity of uterine bleeding\n Def: A condition of the genital system affecting females, caused by hormonal disturbances. This condition is characterised by abnormal menstruation, with a between cycle variation of 2-20 days....\n --PARENT--> [GA20] Menstrual cycle bleeding disorders\n --CHILD--> [GA20.2] Ovulation bleeding\n Def: A condition of the genital system affecting females, caused by natural and routine fluctuations in endocrine hormones. This condition is characterised by recurrent and cyclic bleeding of the uterine l...", "[GA20.3] Abnormal regularity of uterine bleeding\n Def: A condition of the genital system affecting females, caused by hormonal disturbances. This condition is characterised by abnormal menstruation, with a between cycle variation of 2-20 days....\n --PARENT--> [GA20] Menstrual cycle bleeding disorders\n --CHILD--> [GA20.1] Abnormal frequency of uterine bleeding\n Def: Any condition of the genital system affecting females, caused by hormonal disturbances. These conditions are characterised by menstrual bleeding episodes that occur with increased frequency or are del...", "[8C74.1Z] Periodic paralysis, unspecified\n --PARENT--> [8C74.1] Periodic paralysis\n Def: Rare group of neuromuscular disorders that are associated with defects in ion channels. Characterized by intermittent episodes of severe weakness of the limbs usually after heavy exercise, fasting, or...\n --CHILD--> [8C74.11] Hyperkalaemic periodic paralysis\n Def: Hyperkalaemic periodic paralysis (HyperPP) is a muscle disorder characterised by episodic attacks of muscle weakness associated with an increase in serum potassium concentration....", "[8C74.1Z] Periodic paralysis, unspecified\n --PARENT--> [8C74.1] Periodic paralysis\n Def: Rare group of neuromuscular disorders that are associated with defects in ion channels. Characterized by intermittent episodes of severe weakness of the limbs usually after heavy exercise, fasting, or...\n --CHILD--> [8C74.1Y] Other specified periodic paralysis" ]
4A60.0
Familial Mediterranean fever
[ { "from_icd11": "4A60.0", "icd10_code": "D8982", "icd10_title": "Autoimmune lymphoproliferative syndrome [ALPS]" }, { "from_icd11": "4A60.0", "icd10_code": "D89813", "icd10_title": "Graft-versus-host disease, unspecified" }, { "from_icd11": "4A60.0", "icd10_code": "D89810", "icd10_title": "Acute graft-versus-host disease" }, { "from_icd11": "4A60.0", "icd10_code": "D89811", "icd10_title": "Chronic graft-versus-host disease" }, { "from_icd11": "4A60.0", "icd10_code": "D8989", "icd10_title": "Other specified disorders involving the immune mechanism, not elsewhere classified" }, { "from_icd11": "4A60.0", "icd10_code": "D89812", "icd10_title": "Acute on chronic graft-versus-host disease" }, { "from_icd11": "4A60.0", "icd10_code": "D898", "icd10_title": "Other specified disorders involving the immune mechanism, not elsewhere classified" }, { "from_icd11": "GA20.3", "icd10_code": "N926", "icd10_title": "Irregular menstruation, unspecified" }, { "from_icd11": "GA20.3", "icd10_code": "N925", "icd10_title": "Other specified irregular menstruation" }, { "from_icd11": "8C74.1Z", "icd10_code": "G723", "icd10_title": "Periodic paralysis" }, { "from_icd11": "QC4Y", "icd10_code": "Z86718", "icd10_title": "Personal history of other venous thrombosis and embolism" }, { "from_icd11": "QC4Y", "icd10_code": "Z9181", "icd10_title": "History of falling" }, { "from_icd11": "QA43.Z", "icd10_code": "Z35", "icd10_title": "" }, { "from_icd11": "QA43.Z", "icd10_code": "Z354", "icd10_title": "" }, { "from_icd11": "QA43.Z", "icd10_code": "Z358", "icd10_title": "" } ]
D8982
Autoimmune lymphoproliferative syndrome [ALPS]
An oncology consult was requested for evaluation of suspected lymphoproliferative malignancies. A rheumatology consult was also requested for inflammatory polyarthritis and given her history of AOSD. On admission, laboratory data showed WBC 10,610/ml, platelet count 512,000/ml, C-reactive protein (CRP) 58 mg/dl, erythrocyte sedimentation rate (ESR) 84 mm/h. Liver function tests were within normal limit. The serum ferritin level was 962 ng/ml. Specific connective tissue disease serologies were all negative including antinuclear antibody (ANA) and rheumatoid factor. Other tests that were negative included, HIV test, Lyme Ab, Epstein-Barr virus (EBV) IgM, hepatitis B and C. During the hospital stay, the patient had intermittent fever. Chest X-ray was negative for any infiltrates, CT chest of abdomen and pelvis with intravenous (IV) contrast was done for evaluation of lymphadenopathy which was also negative for any infectious focus. Urinalysis was unremarkable, urine culture, and blood cultures were negative. CT scan of neck with IV contrast showed extensive multilevel bilateral cervical lymphadenopathy with the largest one measuring approximately 2.2 x 3.5 cm in the right submandibular region . CT scan of chest with IV contrast showed bulky bilateral axillary lymphadenopathy with the largest lymph node measuring 3.1 x 2.4 cm in the right axilla . Mild hepatosplenomegaly was also noted on CT imaging.
3.785156
0.980957
sec[1]/p[2]
en
0.999997
34367773
https://doi.org/10.7759/cureus.16163
[ "chest", "contrast", "lymphadenopathy", "consult", "requested", "scan", "largest", "measuring", "oncology", "suspected" ]
[ { "code": "CB7Z", "title": "Diseases of the respiratory system, unspecified" }, { "code": "CB27", "title": "Pleural effusion" }, { "code": "CA44", "title": "Pyothorax" }, { "code": "MD30.Z", "title": "Chest pain, unspecified" }, { "code": "NA80.Y&XJ1C6", "title": "Thoracic haematoma" }, { "code": "9D43", "title": "Impairment of contrast vision" }, { "code": "QA00.6Y", "title": "Other specified examination of eyes or vision" }, { "code": "NE60", "title": "Harmful effects of drugs, medicaments or biological substances, not elsewhere classified" }, { "code": "PB28", "title": "Unintentional exposure to or harmful effects of other or unspecified drug, medicament or biological substance" }, { "code": "PC98", "title": "Intentional self-harm by exposure to other or unspecified drug, medicament or biological substance" } ]
=== ICD-11 CODES FOUND === [CB7Z] Diseases of the respiratory system, unspecified Also known as: Diseases of the respiratory system, unspecified | disorder of respiratory system | respiratory disease NOS | respiratory tract disease | respiratory disorder NOS [CB27] Pleural effusion Definition: Presence of fluid in the pleural cavity resulting from excessive transudation or exudation from the pleural surfaces. Also known as: Pleural effusion | PE - [pleural effusion] | Pleurisy with effusion | pleurisy with effusion NOS | pleural effusion with transudate Includes: Pleurisy with effusion Excludes: Tuberculosis of the respiratory system | Chylous effusion | Pleurisy [CA44] Pyothorax Definition: Suppurative inflammation of the pleural space, typically due to acute bacterial infection. It can occur as a complication of pneumonia, thoracotomy, abscesses (lung, hepatic, or subdiaphragmatic), or penetrating trauma with a secondary infection. Also known as: Pyothorax | empyema | pyopneumothorax | Pyothorax with fistula | empyema with fistula Includes: empyema | pyopneumothorax Excludes: due to tuberculosis [MD30.Z] Chest pain, unspecified Also known as: Chest pain, unspecified | Pain in throat or chest | chest pain NOS | pain in chest | chest pressure [9D43] Impairment of contrast vision Definition: Contrast sensitivity refers to the ability to distinguish small differences in brightness between adjacent surfaces. Peak Contrast sensitivity refers to the smallest differences that are discernible for large stimuli. For smaller objects, such as those involved in many Activities of Daily Living, contrast sensitivity interacts with visual acuity and visual field. Better contrast makes smaller details visible. The visual field is larger for stronger stimuli. Also known as: Impairment of contrast vision | Moderate impairment of contrast vision | Profound impairment of contrast vision [QA00.6Y] Other specified examination of eyes or vision Also known as: Other specified examination of eyes or vision | No Impairment of Contrast vision | Normal colour vision | No Impairment of Dark adaptation | No diplopia [NE60] Harmful effects of drugs, medicaments or biological substances, not elsewhere classified Also known as: Harmful effects of drugs, medicaments or biological substances, not elsewhere classified | drugs, medicaments or biological substances, toxicity not elsewhere classified | adverse drug effects | drug reaction NOS | drug allergy NOS Excludes: Alcohol intoxication | pathological drug intoxication | hypersensitivity reaction to correctly administered drug [PB28] Unintentional exposure to or harmful effects of other or unspecified drug, medicament or biological substance Also known as: Unintentional exposure to or harmful effects of other or unspecified drug, medicament or biological substance | accidental overdose of other or unspecified drug, medicament or biological substance | accidental poisoning by other or unspecified drug, medicament or biological substance | other or unspecified drug, medicament or biological substance taken in error | accidental drug overdose [PC98] Intentional self-harm by exposure to other or unspecified drug, medicament or biological substance Also known as: Intentional self-harm by exposure to other or unspecified drug, medicament or biological substance | Intentional self-poisoning by and exposure to other or unspecified drug, medicament or biological substance | Intentional overdose of other or unspecified drug, medicament or biological substance | self-administered overdose by drugs | Intentional self-harm by exposure to or harmful effects of systemic antibiotics === GRAPH WALKS === --- Walk 1 --- [CB7Z] Diseases of the respiratory system, unspecified --PARENT--> [12] Diseases of the respiratory system --EXCLUDES--> [?] Endocrine, nutritional or metabolic diseases Def: This chapter includes endocrine diseases, nutritional diseases as well as metabolic diseases.... --- Walk 2 --- [CB7Z] Diseases of the respiratory system, unspecified --PARENT--> [12] Diseases of the respiratory system --RELATED_TO--> [?] Sleep-related breathing disorders Def: Sleep related breathing disorders are characterised by abnormalities of respiration during sleep. In some of these disorders, respiration is also abnormal during wakefulness. The disorders are grouped... --- Walk 3 --- [CB27] Pleural effusion Def: Presence of fluid in the pleural cavity resulting from excessive transudation or exudation from the pleural surfaces.... --EXCLUDES--> [?] Tuberculosis of the respiratory system Def: This is a progressive or chronic disease resulting from infection with the bacterium Mycobacterium tuberculosis or other bacteria in the M. tuberculosis complex: M. bovis, M. africanum, M. canetti, M.... --CHILD--> [?] Respiratory tuberculosis, confirmed Def: A disease of the respiratory tract, caused by an infection with the bacteria Mycobacterium tuberculosis, which has been confirmed by laboratory testing. This disease is characterised by chronic cough,... --- Walk 4 --- [CB27] Pleural effusion Def: Presence of fluid in the pleural cavity resulting from excessive transudation or exudation from the pleural surfaces.... --PARENT--> [?] Pleural, diaphragm or mediastinal disorders Def: Pleural, diaphragm and mediastinal disorders are disorders of the potential space between the two pleura (visceral and parietal) of the lungs, disorders of the diaphragm and mediastinum. The mediastin... --CHILD--> [CB21] Pneumothorax Def: Pneumothorax is an abnormal collection of air or gas in the pleural space that separates the lung from the chest wall, and that may interfere with normal breathing.... --- Walk 5 --- [CA44] Pyothorax Def: Suppurative inflammation of the pleural space, typically due to acute bacterial infection. It can occur as a complication of pneumonia, thoracotomy, abscesses (lung, hepatic, or subdiaphragmatic), or ... --EXCLUDES--> [?] Tuberculous pleurisy, without mention of bacteriological or histological confirmation Def: This is a common, and in many cases lethal, infectious disease caused by various strains of mycobacteria, usually Mycobacterium tuberculosis, with an inflammation of the pleura. This diagnosis is with... --CHILD--> [?] Tuberculous empyema, without mention of bacteriological or histological confirmation --- Walk 6 --- [CA44] Pyothorax Def: Suppurative inflammation of the pleural space, typically due to acute bacterial infection. It can occur as a complication of pneumonia, thoracotomy, abscesses (lung, hepatic, or subdiaphragmatic), or ... --PARENT--> [?] Lung infections Def: Any condition of the lungs, caused by an infection with a bacterial, viral, fungal, or parasitic source.... --CHILD--> [CA42] Acute bronchitis Def: An acute disease of the bronchi, commonly caused by an infection with a bacterial or viral source. This disease is characterised by inflammation of the bronchi. This disease presents with cough, wheez...
[ "[CB7Z] Diseases of the respiratory system, unspecified\n --PARENT--> [12] Diseases of the respiratory system\n --EXCLUDES--> [?] Endocrine, nutritional or metabolic diseases\n Def: This chapter includes endocrine diseases, nutritional diseases as well as metabolic diseases....", "[CB7Z] Diseases of the respiratory system, unspecified\n --PARENT--> [12] Diseases of the respiratory system\n --RELATED_TO--> [?] Sleep-related breathing disorders\n Def: Sleep related breathing disorders are characterised by abnormalities of respiration during sleep. In some of these disorders, respiration is also abnormal during wakefulness. The disorders are grouped...", "[CB27] Pleural effusion\n Def: Presence of fluid in the pleural cavity resulting from excessive transudation or exudation from the pleural surfaces....\n --EXCLUDES--> [?] Tuberculosis of the respiratory system\n Def: This is a progressive or chronic disease resulting from infection with the bacterium Mycobacterium tuberculosis or other bacteria in the M. tuberculosis complex: M. bovis, M. africanum, M. canetti, M....\n --CHILD--> [?] Respiratory tuberculosis, confirmed\n Def: A disease of the respiratory tract, caused by an infection with the bacteria Mycobacterium tuberculosis, which has been confirmed by laboratory testing. This disease is characterised by chronic cough,...", "[CB27] Pleural effusion\n Def: Presence of fluid in the pleural cavity resulting from excessive transudation or exudation from the pleural surfaces....\n --PARENT--> [?] Pleural, diaphragm or mediastinal disorders\n Def: Pleural, diaphragm and mediastinal disorders are disorders of the potential space between the two pleura (visceral and parietal) of the lungs, disorders of the diaphragm and mediastinum. The mediastin...\n --CHILD--> [CB21] Pneumothorax\n Def: Pneumothorax is an abnormal collection of air or gas in the pleural space that separates the lung from the chest wall, and that may interfere with normal breathing....", "[CA44] Pyothorax\n Def: Suppurative inflammation of the pleural space, typically due to acute bacterial infection. It can occur as a complication of pneumonia, thoracotomy, abscesses (lung, hepatic, or subdiaphragmatic), or ...\n --EXCLUDES--> [?] Tuberculous pleurisy, without mention of bacteriological or histological confirmation\n Def: This is a common, and in many cases lethal, infectious disease caused by various strains of mycobacteria, usually Mycobacterium tuberculosis, with an inflammation of the pleura. This diagnosis is with...\n --CHILD--> [?] Tuberculous empyema, without mention of bacteriological or histological confirmation", "[CA44] Pyothorax\n Def: Suppurative inflammation of the pleural space, typically due to acute bacterial infection. It can occur as a complication of pneumonia, thoracotomy, abscesses (lung, hepatic, or subdiaphragmatic), or ...\n --PARENT--> [?] Lung infections\n Def: Any condition of the lungs, caused by an infection with a bacterial, viral, fungal, or parasitic source....\n --CHILD--> [CA42] Acute bronchitis\n Def: An acute disease of the bronchi, commonly caused by an infection with a bacterial or viral source. This disease is characterised by inflammation of the bronchi. This disease presents with cough, wheez..." ]
CB7Z
Diseases of the respiratory system, unspecified
[ { "from_icd11": "CB7Z", "icd10_code": "J989", "icd10_title": "Respiratory disorder, unspecified" }, { "from_icd11": "CB7Z", "icd10_code": "X", "icd10_title": "" }, { "from_icd11": "CB7Z", "icd10_code": "J09-J18", "icd10_title": "" }, { "from_icd11": "CB27", "icd10_code": "J910", "icd10_title": "Malignant pleural effusion" }, { "from_icd11": "CB27", "icd10_code": "J918", "icd10_title": "Pleural effusion in other conditions classified elsewhere" }, { "from_icd11": "CB27", "icd10_code": "J90", "icd10_title": "Pleural effusion, not elsewhere classified" }, { "from_icd11": "CB27", "icd10_code": "J90-J94", "icd10_title": "" }, { "from_icd11": "CB27", "icd10_code": "J91", "icd10_title": "Pleural effusion in conditions classified elsewhere" }, { "from_icd11": "CA44", "icd10_code": "J869", "icd10_title": "Pyothorax without fistula" }, { "from_icd11": "CA44", "icd10_code": "J860", "icd10_title": "Pyothorax with fistula" }, { "from_icd11": "CA44", "icd10_code": "J85-J86", "icd10_title": "" }, { "from_icd11": "CA44", "icd10_code": "J86", "icd10_title": "Pyothorax" }, { "from_icd11": "MD30.Z", "icd10_code": "R0781", "icd10_title": "Pleurodynia" }, { "from_icd11": "MD30.Z", "icd10_code": "R0782", "icd10_title": "Intercostal pain" }, { "from_icd11": "MD30.Z", "icd10_code": "R079", "icd10_title": "Chest pain, unspecified" } ]
J989
Respiratory disorder, unspecified
The treatment comprised anti-heart failure, anti-hypertension, and surgical therapy. Figure 1A depicts the BP changes during the entire treatment period. Her BP was still considerably raised six hours after admission, and it showed no signs of lowering. Therefore, we stopped the milrinone infusion and oral spironolactone tablets, and kept treating refractory hypertension with the vasodilator sodium nitroprusside and the adrenergic α blocker phentolamine for 10 days. During this period, SBP was up to 266 mmHg and DBP was up to 159 mmHg. Amlodipine, in combination with sodium nitroprusside and phentolamine, was used to stabilize BP before tumor resection, followed by captopril and sodium nitroprusside. On the 27th day, we stopped the sodium nitroprusside, and switched to furosemide, spironolactone, metoprolol tartrate, captopril, and amlodipine tablets for 15 days. Then BP was sustained at 110–130/70–100 mmHg, and the values of catecholamines in urine were all returned to normal ( Supplementary Table S1 ). After a subsequent follow-up of 3 months, her transthoracic echocardiography showed that the left ventricular wall became thinner than before, and left ventricular systolic function returned to normal . After 7 months, her transthoracic echocardiography and hs-cTnT values were restored . This implied that the catecholamine cardiomyopathy induced severe decline in heart function had been reversed.
3.980469
0.95752
sec[1]/p[5]
en
0.999996
PMC9947659
https://doi.org/10.3389/fped.2023.1063795
[ "sodium", "nitroprusside", "mmhg", "anti", "heart", "hypertension", "period", "spironolactone", "tablets", "phentolamine" ]
[ { "code": "5C72", "title": "Hypo-osmolality or hyponatraemia" }, { "code": "5C71", "title": "Hyperosmolality or hypernatraemia" }, { "code": "5C64.6", "title": "Disorders of sodium metabolism" }, { "code": "5B5K.5", "title": "Sodium chloride deficiency" }, { "code": "5B91.2", "title": "Sodium chloride excess" }, { "code": "JA86.Y", "title": "Maternal care for other specified fetal problems" }, { "code": "MB23.1", "title": "Antisocial behaviour" }, { "code": "3B4Z", "title": "Coagulation defects, unspecified" }, { "code": "4A45.Z", "title": "Antiphospholipid syndrome, unspecified" }, { "code": "4A43.Y", "title": "Other specified overlap non-organ specific systemic autoimmune disease" } ]
=== ICD-11 CODES FOUND === [5C72] Hypo-osmolality or hyponatraemia Definition: Serum sodium concentrations of less than 135 mEq/L; decreased serum concentration of osmotically active particles Also known as: Hypo-osmolality or hyponatraemia | hypo-osmolality | hyponatraemia | hyponatremia syndrome | hyponatremic Includes: sodium [na] deficiency Excludes: Syndrome of inappropriate secretion of antidiuretic hormone [5C71] Hyperosmolality or hypernatraemia Definition: Serum sodium concentrations in excess of 145 mmol/L; increased serum concentration of osmotically active particles Also known as: Hyperosmolality or hypernatraemia | Hyperosmolality | hyperosmolality syndrome | nonketotic hyperosmolar syndrome | hyperosmolar syndrome [5C64.6] Disorders of sodium metabolism Also known as: Disorders of sodium metabolism [5B5K.5] Sodium chloride deficiency Definition: Sodium and chloride are usually found together in most foods as sodium chloride, also termed salt. For that reason, the effects of sodium and chloride deficiency are considered together. Deficiency can be caused by poor intake or increased losses (e.g., diuretics increase the urinary excretion of water, sodium, and chloride; in cystic fibrosis the sodium and chloride content of sweat is very high; gastrointestinal losses are associated with diarrhoeal diseases, emesis, ostomy output and other ca Also known as: Sodium chloride deficiency [5B91.2] Sodium chloride excess Definition: The main adverse effect of increased sodium chloride in the diet is increased blood pressure, which is a major risk factor for cardiovascular-renal diseases. However, evidence from a variety of studies, including observational studies and clinical trials, has demonstrated heterogeneity in the blood pressure responses to sodium intake. Those individuals with the greatest reductions in blood pressure in response to decreased sodium intake are termed “salt sensitive”. Also known as: Sodium chloride excess [JA86.Y] Maternal care for other specified fetal problems Also known as: Maternal care for other specified fetal problems | Maternal care for other isoimmunization | Isoimmunization NOS | maternal antibodies NOS | pregnancy management affected by incompatibility of blood groups NOS [MB23.1] Antisocial behaviour Definition: Behaviour in which the basic rights of others or major age-appropriate societal norms, rules, or laws, are violated. Also known as: Antisocial behaviour | Child or adolescent antisocial behaviour [3B4Z] Coagulation defects, unspecified Also known as: Coagulation defects, unspecified | blood clotting disturbance | blood clotting defect | blood clotting factor deficiency | clotting abnormality [4A45.Z] Antiphospholipid syndrome, unspecified Also known as: Antiphospholipid syndrome, unspecified | Antiphospholipid syndrome | Hughes syndrome | Anticardiolipin syndrome [4A43.Y] Other specified overlap non-organ specific systemic autoimmune disease Also known as: Other specified overlap non-organ specific systemic autoimmune disease | Antisynthetase syndrome | Reynolds syndrome | Syndromic multisystem autoimmune disease due to ITCH deficiency | Eosinophilia myalgia syndrome === GRAPH WALKS === --- Walk 1 --- [5C72] Hypo-osmolality or hyponatraemia Def: Serum sodium concentrations of less than 135 mEq/L; decreased serum concentration of osmotically active particles... --RELATED_TO--> [?] Hyponatremia of newborn Def: Hyponatremia is defined as serum sodium less than 130 mmol/L... --PARENT--> [?] Disturbances of sodium balance of newborn Def: A paediatric condition characterised by abnormally high or low levels of sodium in the blood in a newborn, when the normal range is defined as 135 to 150 mEq/L.... --- Walk 2 --- [5C72] Hypo-osmolality or hyponatraemia Def: Serum sodium concentrations of less than 135 mEq/L; decreased serum concentration of osmotically active particles... --EXCLUDES--> [?] Syndrome of inappropriate secretion of antidiuretic hormone Def: Syndrome of inappropriate antidiuretic hormone (ADH) secretion (SIADH) is characterised by continued ADH secretion, leading to hyponatremia, hypoosmolality and natriuresis. Exact prevalence is unknown... --CHILD--> [?] Nephrogenic syndrome of inappropriate antidiuresis --- Walk 3 --- [5C71] Hyperosmolality or hypernatraemia Def: Serum sodium concentrations in excess of 145 mmol/L; increased serum concentration of osmotically active particles... --RELATED_TO--> [?] Hypernatremia of newborn Def: Hypernatremia is defined as serum sodium greater than 145 mmol/L.... --PARENT--> [?] Hyperosmolality or hypernatraemia Def: Serum sodium concentrations in excess of 145 mmol/L; increased serum concentration of osmotically active particles... --- Walk 4 --- [5C71] Hyperosmolality or hypernatraemia Def: Serum sodium concentrations in excess of 145 mmol/L; increased serum concentration of osmotically active particles... --RELATED_TO--> [?] Hypernatremia of newborn Def: Hypernatremia is defined as serum sodium greater than 145 mmol/L.... --PARENT--> [?] Disturbances of sodium balance of newborn Def: A paediatric condition characterised by abnormally high or low levels of sodium in the blood in a newborn, when the normal range is defined as 135 to 150 mEq/L.... --- Walk 5 --- [5C64.6] Disorders of sodium metabolism --RELATED_TO--> [?] Congenital sodium diarrhoea Def: Congenital sodium diarrhoea is a congenital intestinal transport defect characterised by severe watery diarrhoea containing high concentrations of sodium, hyponatremia and metabolic acidosis. This is ... --PARENT--> [?] Congenital intestinal transport defect Def: This is a congenital disease of the small intestinal mucosa that presents with intractable diarrhoea and malabsorption of nutrients in young children, due to defect of transporter of nutrients in ente... --- Walk 6 --- [5C64.6] Disorders of sodium metabolism --RELATED_TO--> [?] Congenital sodium diarrhoea Def: Congenital sodium diarrhoea is a congenital intestinal transport defect characterised by severe watery diarrhoea containing high concentrations of sodium, hyponatremia and metabolic acidosis. This is ... --PARENT--> [?] Disorders of sodium metabolism
[ "[5C72] Hypo-osmolality or hyponatraemia\n Def: Serum sodium concentrations of less than 135 mEq/L; decreased serum concentration of osmotically active particles...\n --RELATED_TO--> [?] Hyponatremia of newborn\n Def: Hyponatremia is defined as serum sodium less than 130 mmol/L...\n --PARENT--> [?] Disturbances of sodium balance of newborn\n Def: A paediatric condition characterised by abnormally high or low levels of sodium in the blood in a newborn, when the normal range is defined as 135 to 150 mEq/L....", "[5C72] Hypo-osmolality or hyponatraemia\n Def: Serum sodium concentrations of less than 135 mEq/L; decreased serum concentration of osmotically active particles...\n --EXCLUDES--> [?] Syndrome of inappropriate secretion of antidiuretic hormone\n Def: Syndrome of inappropriate antidiuretic hormone (ADH) secretion (SIADH) is characterised by continued ADH secretion, leading to hyponatremia, hypoosmolality and natriuresis. Exact prevalence is unknown...\n --CHILD--> [?] Nephrogenic syndrome of inappropriate antidiuresis", "[5C71] Hyperosmolality or hypernatraemia\n Def: Serum sodium concentrations in excess of 145 mmol/L; increased serum concentration of osmotically active particles...\n --RELATED_TO--> [?] Hypernatremia of newborn\n Def: Hypernatremia is defined as serum sodium greater than 145 mmol/L....\n --PARENT--> [?] Hyperosmolality or hypernatraemia\n Def: Serum sodium concentrations in excess of 145 mmol/L; increased serum concentration of osmotically active particles...", "[5C71] Hyperosmolality or hypernatraemia\n Def: Serum sodium concentrations in excess of 145 mmol/L; increased serum concentration of osmotically active particles...\n --RELATED_TO--> [?] Hypernatremia of newborn\n Def: Hypernatremia is defined as serum sodium greater than 145 mmol/L....\n --PARENT--> [?] Disturbances of sodium balance of newborn\n Def: A paediatric condition characterised by abnormally high or low levels of sodium in the blood in a newborn, when the normal range is defined as 135 to 150 mEq/L....", "[5C64.6] Disorders of sodium metabolism\n --RELATED_TO--> [?] Congenital sodium diarrhoea\n Def: Congenital sodium diarrhoea is a congenital intestinal transport defect characterised by severe watery diarrhoea containing high concentrations of sodium, hyponatremia and metabolic acidosis. This is ...\n --PARENT--> [?] Congenital intestinal transport defect\n Def: This is a congenital disease of the small intestinal mucosa that presents with intractable diarrhoea and malabsorption of nutrients in young children, due to defect of transporter of nutrients in ente...", "[5C64.6] Disorders of sodium metabolism\n --RELATED_TO--> [?] Congenital sodium diarrhoea\n Def: Congenital sodium diarrhoea is a congenital intestinal transport defect characterised by severe watery diarrhoea containing high concentrations of sodium, hyponatremia and metabolic acidosis. This is ...\n --PARENT--> [?] Disorders of sodium metabolism" ]
5C72
Hypo-osmolality or hyponatraemia
[ { "from_icd11": "5C72", "icd10_code": "E871", "icd10_title": "Hypo-osmolality and hyponatremia" }, { "from_icd11": "5C71", "icd10_code": "E870", "icd10_title": "Hyperosmolality and hypernatremia" }, { "from_icd11": "5B5K.5", "icd10_code": "E618", "icd10_title": "Deficiency of other specified nutrient elements" }, { "from_icd11": "5B91.2", "icd10_code": "E678", "icd10_title": "Other specified hyperalimentation" }, { "from_icd11": "JA86.Y", "icd10_code": "O26841 ", "icd10_title": "" }, { "from_icd11": "JA86.Y", "icd10_code": "O26843 ", "icd10_title": "" }, { "from_icd11": "JA86.Y", "icd10_code": "O26849 ", "icd10_title": "" }, { "from_icd11": "JA86.Y", "icd10_code": "O3680X0 ", "icd10_title": "" }, { "from_icd11": "3B4Z", "icd10_code": "D688", "icd10_title": "Other specified coagulation defects" }, { "from_icd11": "3B4Z", "icd10_code": "D689", "icd10_title": "Coagulation defect, unspecified" }, { "from_icd11": "3B4Z", "icd10_code": "D699", "icd10_title": "Hemorrhagic condition, unspecified" }, { "from_icd11": "3B4Z", "icd10_code": "D698", "icd10_title": "Other specified hemorrhagic conditions" }, { "from_icd11": "3B4Z", "icd10_code": "D65-D69", "icd10_title": "" }, { "from_icd11": "3B4Z", "icd10_code": "D69", "icd10_title": "Purpura and other hemorrhagic conditions" }, { "from_icd11": "4A45.Z", "icd10_code": "D6861", "icd10_title": "Antiphospholipid syndrome" } ]
E871
Hypo-osmolality and hyponatremia
Staging was done for him, which came back negative for both bone and intra-abdominal metastasis. The case was discussed in our tumor board meeting and the decision was made to go for surgical resection. Laparotomy was done on July 2022. Upon exploration, the tumor was found to be unresectable due to its invasion into the anterior abdominal wall and the lateral pelvic wall so the patient was closed without any intervention. Postop, the patient was referred to oncology for palliative chemotherapy where he received six cycles of palliative gemcitabine and Carboplatin with a 25% dose reduction secondary to grade 4 myelotoxicity. The patient has been receiving avelumab after the stabilization of his condition. Then, the patient was referred to radiation oncology due to pain, for which he was given 21-Gy radiation therapy over three fractions. During follow-up, he developed bilateral hydronephrosis. Therefore, a bilateral nephrostomy was inserted, which result in the stabilization of the creatinine level. The final tumor node metastasis (TNM) staging for him was T4 N0 M0. The patient kept regular follow-ups with medical oncology till he passed away three years after the diagnosis. He was admitted due to small bowel obstruction for which he underwent exploratory laparotomy, right hemicolectomy, and the Hartmann procedure. The patient was kept in the ICU till his death, which was due to a cardiac arrest.
3.472656
0.98584
sec[1]/p[4]
en
0.999999
PMC10022250
https://doi.org/10.7759/cureus.36278
[ "which", "tumor", "oncology", "staging", "abdominal", "metastasis", "laparotomy", "wall", "referred", "palliative" ]
[ { "code": "BD50.41", "title": "Abdominal aortic aneurysm with rupture" }, { "code": "EK91", "title": "Dermatoses which may presage cutaneous lymphoma" }, { "code": "MH12.1", "title": "Death occurring less than 24 hours from onset of symptoms, not otherwise explained" }, { "code": "8A44.3", "title": "Certain specified leukodystrophies" }, { "code": "2F9Z", "title": "Neoplasms of unknown behaviour of unspecified site" }, { "code": "ME61", "title": "Subcutaneous swelling, mass or lump of uncertain or unspecified nature" }, { "code": "2E6Z", "title": "Carcinoma in situ of unspecified site" }, { "code": "2F91.1", "title": "Neoplasms of unknown behaviour of trachea, bronchus or lung" }, { "code": "2F92", "title": "Neoplasms of unknown behaviour of skin" }, { "code": "9B71.3&XS5S", "title": "Retinopathy of prematurity, Stage 2" } ]
=== ICD-11 CODES FOUND === [BD50.41] Abdominal aortic aneurysm with rupture Also known as: Abdominal aortic aneurysm with rupture | abdominal aorta aneurysm rupture | abdominal aorta aneurysm ruptured | abdominal aortic aneurysm which has ruptured | ruptured AAA [EK91] Dermatoses which may presage cutaneous lymphoma Definition: Dermatoses which may represent the earliest stages of cutaneous lymphoma but where it is not possible to confirm their neoplastic nature. Also known as: Dermatoses which may presage cutaneous lymphoma [MH12.1] Death occurring less than 24 hours from onset of symptoms, not otherwise explained Also known as: Death occurring less than 24 hours from onset of symptoms, not otherwise explained | died without sign of disease | Death known not to be violent or instantaneous for which no cause can be discovered | death known not to be violent or instantaneous, cause unknown | Death without sign of disease Includes: Death known not to be violent or instantaneous for which no cause can be discovered | Death without sign of disease [8A44.3] Certain specified leukodystrophies Also known as: Certain specified leukodystrophies | CACH syndrome | Vanishing white matter disease | Childhood ataxia with central nervous system hypomyelination | Congenital or early infantile CACH syndrome [2F9Z] Neoplasms of unknown behaviour of unspecified site Also known as: Neoplasms of unknown behaviour of unspecified site | neoplasia | neoplasm growth NOS | tumour of unspecified site | tumourlet of unspecified site [ME61] Subcutaneous swelling, mass or lump of uncertain or unspecified nature Definition: One or more localised subcutaneous soft tissue masses of undetermined or unspecified nature Also known as: Subcutaneous swelling, mass or lump of uncertain or unspecified nature | localised swelling, mass or lump of skin and subcutaneous tissue | localised subcutaneous nodules | subcutaneous nodules | superficial subcutaneous nodules Excludes: localized adiposity | mass and lump: breast | enlarged lymph nodes [2E6Z] Carcinoma in situ of unspecified site Also known as: Carcinoma in situ of unspecified site | carcinoma in situ of unspecified site | carcinoma in situ NOS | carcinoma in situ | in situ neoplasm [2F91.1] Neoplasms of unknown behaviour of trachea, bronchus or lung Also known as: Neoplasms of unknown behaviour of trachea, bronchus or lung | trachea, bronchus or lung tumour NOS | Intravascular bronchial alveolar tumour of unspecified site | Bronchial adenoma of unknown behaviour of unspecified site | Intravascular bronchial alveolar tumour unknown behaviour of unspecified site [2F92] Neoplasms of unknown behaviour of skin Also known as: Neoplasms of unknown behaviour of skin | skin tumour NOS === GRAPH WALKS === --- Walk 1 --- [BD50.41] Abdominal aortic aneurysm with rupture --PARENT--> [BD50.4] Abdominal aortic aneurysm --PARENT--> [BD50] Aortic aneurysm or dissection Def: Aortic aneurysm is a term for any swelling (dilation or aneurysm) of the aorta to greater than 1.5 times normal, usually representing an underlying weakness in the wall of the aorta at that location. ... --- Walk 2 --- [BD50.41] Abdominal aortic aneurysm with rupture --PARENT--> [BD50.4] Abdominal aortic aneurysm --CHILD--> [BD50.4Z] Abdominal aortic aneurysm, without mention of perforation or rupture --- Walk 3 --- [EK91] Dermatoses which may presage cutaneous lymphoma Def: Dermatoses which may represent the earliest stages of cutaneous lymphoma but where it is not possible to confirm their neoplastic nature.... --CHILD--> [EK91.2] Primary cutaneous plasmacytosis Def: A skin disorder resulting from focal or multifocal dense infiltration of the skin by plasma cell aggregates. It may be associated with high levels of serum IgG4. It typically presents as widespread re... --PARENT--> [EK91] Dermatoses which may presage cutaneous lymphoma Def: Dermatoses which may represent the earliest stages of cutaneous lymphoma but where it is not possible to confirm their neoplastic nature.... --- Walk 4 --- [EK91] Dermatoses which may presage cutaneous lymphoma Def: Dermatoses which may represent the earliest stages of cutaneous lymphoma but where it is not possible to confirm their neoplastic nature.... --CHILD--> [EK91.1] Poikiloderma vasculare atrophicans Def: Poikiloderma vasculare atrophicans is a cutaneous reaction pattern characterised by mottled hyper- and hypomelanosis, telangiectasia and progressive dermal and epidermal atrophy. It may manifest as a ... --PARENT--> [EK91] Dermatoses which may presage cutaneous lymphoma Def: Dermatoses which may represent the earliest stages of cutaneous lymphoma but where it is not possible to confirm their neoplastic nature.... --- Walk 5 --- [MH12.1] Death occurring less than 24 hours from onset of symptoms, not otherwise explained --PARENT--> [MH12] Other sudden death, cause unknown --CHILD--> [MH12.1] Death occurring less than 24 hours from onset of symptoms, not otherwise explained --- Walk 6 --- [MH12.1] Death occurring less than 24 hours from onset of symptoms, not otherwise explained --PARENT--> [MH12] Other sudden death, cause unknown --CHILD--> [MH12.Y] Other specified sudden death, cause unknown
[ "[BD50.41] Abdominal aortic aneurysm with rupture\n --PARENT--> [BD50.4] Abdominal aortic aneurysm\n --PARENT--> [BD50] Aortic aneurysm or dissection\n Def: Aortic aneurysm is a term for any swelling (dilation or aneurysm) of the aorta to greater than 1.5 times normal, usually representing an underlying weakness in the wall of the aorta at that location. ...", "[BD50.41] Abdominal aortic aneurysm with rupture\n --PARENT--> [BD50.4] Abdominal aortic aneurysm\n --CHILD--> [BD50.4Z] Abdominal aortic aneurysm, without mention of perforation or rupture", "[EK91] Dermatoses which may presage cutaneous lymphoma\n Def: Dermatoses which may represent the earliest stages of cutaneous lymphoma but where it is not possible to confirm their neoplastic nature....\n --CHILD--> [EK91.2] Primary cutaneous plasmacytosis\n Def: A skin disorder resulting from focal or multifocal dense infiltration of the skin by plasma cell aggregates. It may be associated with high levels of serum IgG4. It typically presents as widespread re...\n --PARENT--> [EK91] Dermatoses which may presage cutaneous lymphoma\n Def: Dermatoses which may represent the earliest stages of cutaneous lymphoma but where it is not possible to confirm their neoplastic nature....", "[EK91] Dermatoses which may presage cutaneous lymphoma\n Def: Dermatoses which may represent the earliest stages of cutaneous lymphoma but where it is not possible to confirm their neoplastic nature....\n --CHILD--> [EK91.1] Poikiloderma vasculare atrophicans\n Def: Poikiloderma vasculare atrophicans is a cutaneous reaction pattern characterised by mottled hyper- and hypomelanosis, telangiectasia and progressive dermal and epidermal atrophy. It may manifest as a ...\n --PARENT--> [EK91] Dermatoses which may presage cutaneous lymphoma\n Def: Dermatoses which may represent the earliest stages of cutaneous lymphoma but where it is not possible to confirm their neoplastic nature....", "[MH12.1] Death occurring less than 24 hours from onset of symptoms, not otherwise explained\n --PARENT--> [MH12] Other sudden death, cause unknown\n --CHILD--> [MH12.1] Death occurring less than 24 hours from onset of symptoms, not otherwise explained", "[MH12.1] Death occurring less than 24 hours from onset of symptoms, not otherwise explained\n --PARENT--> [MH12] Other sudden death, cause unknown\n --CHILD--> [MH12.Y] Other specified sudden death, cause unknown" ]
BD50.41
Abdominal aortic aneurysm with rupture
[ { "from_icd11": "BD50.41", "icd10_code": "I713", "icd10_title": "Abdominal aortic aneurysm, ruptured" }, { "from_icd11": "EK91", "icd10_code": "L989", "icd10_title": "Disorder of the skin and subcutaneous tissue, unspecified" }, { "from_icd11": "MH12.1", "icd10_code": "R961", "icd10_title": "" }, { "from_icd11": "2F9Z", "icd10_code": "D487", "icd10_title": "Neoplasm of uncertain behavior of other specified sites" }, { "from_icd11": "2F9Z", "icd10_code": "D482", "icd10_title": "Neoplasm of uncertain behavior of peripheral nerves and autonomic nervous system" }, { "from_icd11": "2F9Z", "icd10_code": "D37-D48", "icd10_title": "" }, { "from_icd11": "2F9Z", "icd10_code": "D377", "icd10_title": "" }, { "from_icd11": "2F9Z", "icd10_code": "D48", "icd10_title": "Neoplasm of uncertain behavior of other and unspecified sites" }, { "from_icd11": "2F9Z", "icd10_code": "D489", "icd10_title": "Neoplasm of uncertain behavior, unspecified" }, { "from_icd11": "ME61", "icd10_code": "R2240", "icd10_title": "Localized swelling, mass and lump, unspecified lower limb" }, { "from_icd11": "ME61", "icd10_code": "R2232", "icd10_title": "Localized swelling, mass and lump, left upper limb" }, { "from_icd11": "ME61", "icd10_code": "R2242", "icd10_title": "Localized swelling, mass and lump, left lower limb" }, { "from_icd11": "ME61", "icd10_code": "R2231", "icd10_title": "Localized swelling, mass and lump, right upper limb" }, { "from_icd11": "ME61", "icd10_code": "R2241", "icd10_title": "Localized swelling, mass and lump, right lower limb" }, { "from_icd11": "ME61", "icd10_code": "R2233", "icd10_title": "Localized swelling, mass and lump, upper limb, bilateral" } ]
I713
Abdominal aortic aneurysm, ruptured
A 25-year-old male with skin type V presented with multiple variably pigmented lesions all over the body since the age of 5. He reported a history of swelling affecting the bilateral nipple-areola complex (NAC) for 1 year. Lesions were foul-smelling and exacerbating during summer. He did not report a similar family history. On cutaneous examination, the bilateral NAC showed erythematous to gray verrucous plaques that hindered the visibility of the nipples . Dermoscopic examination (Dermlite, DL4, 10× magnification) of the NAC revealed a central crater filled with a yellow to yellowish-brown keratotic plug surrounded by white radial streaks, and outermost brown homogenous area and pigment network . The shape of the craters was variable with an angulated border. Histological examination of the plaque over the NAC, revealed a suprabasal acantholysis along with corp ronds and grains . A diagnosis of nevoid hyperkeratosis of nipple and areola (NHNA) secondary to Darier disease (DD) was made. Besides, there were multiple erythematous to gray-brown verrucous papules scattered all over the body, more so in the seborrheic distribution , which revealed a similar dermoscopic pattern irrespective of the size or duration of the lesions . The patient was treated with 30 mg isotretinoin capsules once a day. 2 months post-therapy, NHNA dermoscopic features and cutaneous lesions showed a significant improvement .
4.066406
0.976074
sec[1]/p[0]
en
0.999997
34414005
https://doi.org/10.5826/dpc.1103a44
[ "lesions", "over", "dermoscopic", "brown", "multiple", "body", "nipple", "areola", "similar", "cutaneous" ]
[ { "code": "FA5Z", "title": "Arthropathies, unspecified" }, { "code": "FC0Z", "title": "Diseases of the musculoskeletal system or connective tissue, unspecified" }, { "code": "ME60.Z", "title": "Skin lesion of unspecified nature" }, { "code": "MD41", "title": "Clinical findings on diagnostic imaging of lung" }, { "code": "GC2Z&XA6KU8", "title": "Disease of kidney, not elsewhere classified" }, { "code": "MB22.5", "title": "Increased goal-directed activity" }, { "code": "DA0E.5Y", "title": "Other specified malocclusion" }, { "code": "5B80.0Z", "title": "Overweight, unspecified" }, { "code": "NE60", "title": "Harmful effects of drugs, medicaments or biological substances, not elsewhere classified" }, { "code": "MG43.1", "title": "Overeating" } ]
=== ICD-11 CODES FOUND === [FA5Z] Arthropathies, unspecified Also known as: Arthropathies, unspecified | Disorders affecting predominantly peripheral joints | Disorders affecting predominantly peripheral limb joints | arthropathy NOS | arthropathic [FC0Z] Diseases of the musculoskeletal system or connective tissue, unspecified Also known as: Diseases of the musculoskeletal system or connective tissue, unspecified | bone disease NOS | bone disorder NOS | bone lesion NOS | musculoskeletal complications NOS [ME60.Z] Skin lesion of unspecified nature Also known as: Skin lesion of unspecified nature | Skin lesion of uncertain or unspecified nature | Skin lesion without established diagnosis | Pigmented skin lesion of unspecified nature | Ulcer of skin of unspecified nature [MD41] Clinical findings on diagnostic imaging of lung Definition: Clinical findings on diagnostic imaging of lung is findings on diagnostic imaging of the lung which don't appear in normal status of the body. Diagnostic imaging refers to technologies that doctors use to look inside body for clues about a medical condition. X-rays, CT scans, nuclear medicine scans, MRI scans and ultrasound are all types of diagnostic imaging. Also known as: Clinical findings on diagnostic imaging of lung | abnormal diagnostic imaging of lung | Hyperinflation of lung | Lung mass | Pulmonary lobe mass [MB22.5] Increased goal-directed activity Definition: Increased planning of and participation in multiple activities (e.g. sexual, occupational, political, religious), compared to the individual's typical level of activity. Also known as: Increased goal-directed activity | overactivity | behaviour of overactivity [DA0E.5Y] Other specified malocclusion Also known as: Other specified malocclusion | Crossbite | overbite | openbite | excessive overbite Includes: Crossbite [5B80.0Z] Overweight, unspecified Also known as: Overweight, unspecified | Overweight [NE60] Harmful effects of drugs, medicaments or biological substances, not elsewhere classified Also known as: Harmful effects of drugs, medicaments or biological substances, not elsewhere classified | drugs, medicaments or biological substances, toxicity not elsewhere classified | adverse drug effects | drug reaction NOS | drug allergy NOS Excludes: Alcohol intoxication | pathological drug intoxication | hypersensitivity reaction to correctly administered drug [MG43.1] Overeating Definition: The consumption of excess food in relation to energy and nutritional requirements. Also known as: Overeating | Excessive eating | gluttony | hyperalimentation | Hyperalimentation NOS Includes: Excessive eating Excludes: Bipolar or related disorders | Depressive disorders | Feeding or eating disorders === GRAPH WALKS === --- Walk 1 --- [FA5Z] Arthropathies, unspecified --PARENT--> [?] Arthropathies --CHILD--> [?] Inflammatory arthropathies --- Walk 2 --- [FA5Z] Arthropathies, unspecified --PARENT--> [?] Arthropathies --PARENT--> [15] Diseases of the musculoskeletal system or connective tissue Def: This chapter contains diseases of musculoskeletal system and diseases of connective tissue.... --- Walk 3 --- [FC0Z] Diseases of the musculoskeletal system or connective tissue, unspecified --PARENT--> [15] Diseases of the musculoskeletal system or connective tissue Def: This chapter contains diseases of musculoskeletal system and diseases of connective tissue.... --RELATED_TO--> [?] Nonorgan specific systemic autoimmune disorders --- Walk 4 --- [FC0Z] Diseases of the musculoskeletal system or connective tissue, unspecified --PARENT--> [15] Diseases of the musculoskeletal system or connective tissue Def: This chapter contains diseases of musculoskeletal system and diseases of connective tissue.... --PARENT--> [?] ICD-11 for Mortality and Morbidity Statistics --- Walk 5 --- [ME60.Z] Skin lesion of unspecified nature --PARENT--> [ME60] Skin lesion of uncertain or unspecified nature Def: To be used where there is either significant uncertainty or alternatively no information as to the nature of a circumscribed skin lesion. This is of particular importance with regard to whether or not... --PARENT--> [?] Symptoms or signs involving the skin Def: This category allows the capture of imprecise data where a more specific diagnosis cannot be made or to supplement information about a specific diagnosis.... --- Walk 6 --- [ME60.Z] Skin lesion of unspecified nature --PARENT--> [ME60] Skin lesion of uncertain or unspecified nature Def: To be used where there is either significant uncertainty or alternatively no information as to the nature of a circumscribed skin lesion. This is of particular importance with regard to whether or not... --CHILD--> [ME60.2] Ulcer of skin of uncertain nature Def: This denotes the presence of a skin ulcer but uncertainty as to its nature. No inference as to whether the ulcer might be of serious significance (e.g. suspected skin cancer) is made....
[ "[FA5Z] Arthropathies, unspecified\n --PARENT--> [?] Arthropathies\n --CHILD--> [?] Inflammatory arthropathies", "[FA5Z] Arthropathies, unspecified\n --PARENT--> [?] Arthropathies\n --PARENT--> [15] Diseases of the musculoskeletal system or connective tissue\n Def: This chapter contains diseases of musculoskeletal system and diseases of connective tissue....", "[FC0Z] Diseases of the musculoskeletal system or connective tissue, unspecified\n --PARENT--> [15] Diseases of the musculoskeletal system or connective tissue\n Def: This chapter contains diseases of musculoskeletal system and diseases of connective tissue....\n --RELATED_TO--> [?] Nonorgan specific systemic autoimmune disorders", "[FC0Z] Diseases of the musculoskeletal system or connective tissue, unspecified\n --PARENT--> [15] Diseases of the musculoskeletal system or connective tissue\n Def: This chapter contains diseases of musculoskeletal system and diseases of connective tissue....\n --PARENT--> [?] ICD-11 for Mortality and Morbidity Statistics", "[ME60.Z] Skin lesion of unspecified nature\n --PARENT--> [ME60] Skin lesion of uncertain or unspecified nature\n Def: To be used where there is either significant uncertainty or alternatively no information as to the nature of a circumscribed skin lesion. This is of particular importance with regard to whether or not...\n --PARENT--> [?] Symptoms or signs involving the skin\n Def: This category allows the capture of imprecise data where a more specific diagnosis cannot be made or to supplement information about a specific diagnosis....", "[ME60.Z] Skin lesion of unspecified nature\n --PARENT--> [ME60] Skin lesion of uncertain or unspecified nature\n Def: To be used where there is either significant uncertainty or alternatively no information as to the nature of a circumscribed skin lesion. This is of particular importance with regard to whether or not...\n --CHILD--> [ME60.2] Ulcer of skin of uncertain nature\n Def: This denotes the presence of a skin ulcer but uncertainty as to its nature. No inference as to whether the ulcer might be of serious significance (e.g. suspected skin cancer) is made...." ]
FA5Z
Arthropathies, unspecified
[ { "from_icd11": "FA5Z", "icd10_code": "M00-M25", "icd10_title": "" }, { "from_icd11": "FC0Z", "icd10_code": "XIII", "icd10_title": "" }, { "from_icd11": "ME60.Z", "icd10_code": "L989", "icd10_title": "Disorder of the skin and subcutaneous tissue, unspecified" }, { "from_icd11": "MD41", "icd10_code": "R911", "icd10_title": "Solitary pulmonary nodule" }, { "from_icd11": "MD41", "icd10_code": "R91", "icd10_title": "Abnormal findings on diagnostic imaging of lung" }, { "from_icd11": "MB22.5", "icd10_code": "R463", "icd10_title": "Overactivity" }, { "from_icd11": "5B80.0Z", "icd10_code": "E669", "icd10_title": "Obesity, unspecified" }, { "from_icd11": "NE60", "icd10_code": "T50A95A", "icd10_title": "Adverse effect of other bacterial vaccines, initial encounter" }, { "from_icd11": "NE60", "icd10_code": "T50Z15A", "icd10_title": "Adverse effect of immunoglobulin, initial encounter" }, { "from_icd11": "NE60", "icd10_code": "T50Z95A", "icd10_title": "Adverse effect of other vaccines and biological substances, initial encounter" }, { "from_icd11": "NE60", "icd10_code": "T50A95S", "icd10_title": "Adverse effect of other bacterial vaccines, sequela" }, { "from_icd11": "NE60", "icd10_code": "T50B95A", "icd10_title": "Adverse effect of other viral vaccines, initial encounter" }, { "from_icd11": "NE60", "icd10_code": "T50A25A", "icd10_title": "Adverse effect of mixed bacterial vaccines without a pertussis component, initial encounter" }, { "from_icd11": "NE60", "icd10_code": "T50A91A", "icd10_title": "Poisoning by other bacterial vaccines, accidental (unintentional), initial encounter" }, { "from_icd11": "NE60", "icd10_code": "T498X5A", "icd10_title": "Adverse effect of other topical agents, initial encounter" } ]
M00-M25
A 20-year-old lady presented with history of multiple nodular skin lesions, which were erythematous and were associated with stinging pain, 1-2 cm in size over both the upper and lower limbs and face for the past 1 year. This was associated with a low grade fever, on and off, responsive to antipyretic agents, for the same duration. She had history of pain in both knees at the onset of illness, for a period of 3 months, not associated with swelling, early morning stiffness, or pain in other joints, which was worse during the times she had fever. She had no dryness of eyes or mouth, tingling or numbness of extremities, shortness of breath, cough, chest pain, nasal or ear discharge, epistaxis, hearing loss, abdominal pain, weight loss, diarrhea, or dysuria. She had no foot drop or redness of eyes. She was investigated and found to have anemia (hemoglobin (Hb) 9.9 g%), normal total leucocyte count ((TLC) 6200/mm 3 ), differential leucocyte count ((DLC) neutrophils 50%, lymphocytes 46%) and platelet count ((Plt), 261000/mm 3 ), elevated erythrocyte sedimentation rate ((ESR), 36 mm/hour), and positive rheumatoid factor (RF) in serum by ELISA (26.11 IU, reference 0–15 IU). With this, she was thought to have rheumatoid arthritis and started on methotrexate 5 mg/week, hydroxychloroquine sulfate 200 mg daily, and methylprednisolone 4 mg daily. Subsequently, the skin lesion, fever, and joint pains subsided.
3.847656
0.984863
sec[1]/p[0]
en
0.999998
25580317
https://doi.org/10.1155/2014/641989
[ "pain", "associated", "fever", "count", "skin", "which", "both", "this", "eyes", "loss" ]
[ { "code": "MG3Z", "title": "Pain, unspecified" }, { "code": "8E43.Z", "title": "Pain disorders, unspecified" }, { "code": "MG31.Z", "title": "Acute pain, unspecified" }, { "code": "MG30.Z", "title": "Chronic pain, unspecified" }, { "code": "FB56.2", "title": "Myalgia" }, { "code": "MB25.02", "title": "Disorganised thinking" }, { "code": "LD2F.11", "title": "VATER association" }, { "code": "5A61.0", "title": "Hypopituitarism" }, { "code": "FB1Z", "title": "Conditions associated with the spine, unspecified" }, { "code": "QE5Z", "title": "Problems associated with relationships, unspecified" } ]
=== ICD-11 CODES FOUND === [MG3Z] Pain, unspecified Also known as: Pain, unspecified | pain observations | pain NOS | generalised pain | generalised pain, NOS [8E43.Z] Pain disorders, unspecified Also known as: Pain disorders, unspecified | Pain disorders [MG31.Z] Acute pain, unspecified Also known as: Acute pain, unspecified | Acute pain [MG30.Z] Chronic pain, unspecified Also known as: Chronic pain, unspecified | Chronic pain [FB56.2] Myalgia Definition: This is a disorder characterised by pain in a muscle or group of muscles. Also known as: Myalgia | muscle ache | muscle soreness | muscular pain | myalgic Excludes: Chronic primary musculoskeletal pain | Chronic secondary musculoskeletal pain [MB25.02] Disorganised thinking Definition: A disturbance in the associative thought process typically manifested in speech in which the person shifts suddenly from one topic to another that is unrelated or minimally related to the first. The individual gives no indication of being aware of the disconnectedness or illogicality of their thinking. Also known as: Disorganised thinking | thought derailment | loose associations | disorganised speech [LD2F.11] VATER association Definition: VACTERL/VATER is an association of congenital malformations typically characterised by the presence of at least three of the following: vertebral defects, anal atresia, cardiac defects, tracheo-oesophageal fistula, renal anomalies, and limb abnormalities. Also known as: VATER association | VACTERL association [5A61.0] Hypopituitarism Definition: A disorder manifesting a deficiency or decrease of one or more pituitary hormones, which is caused by a variety of diseases such as tumour, trauma/surgery, irradiation, inflammation and haemorrhage/infarction. Also known as: Hypopituitarism | subpituitarism | hypophyseal dystrophy | hypohypophysism | anterior pituitary insufficiency (in part) Includes: pituitary cachexia | pituitary short stature [FB1Z] Conditions associated with the spine, unspecified Also known as: Conditions associated with the spine, unspecified | dorsopathies | disorder of spine | spinal disorder [QE5Z] Problems associated with relationships, unspecified Also known as: Problems associated with relationships, unspecified === GRAPH WALKS === --- Walk 1 --- [MG3Z] Pain, unspecified --PARENT--> [?] Pain --EXCLUDES--> [?] Abdominal or pelvic pain Def: Pain, an unpleasant distress sensation occurring in varying degrees of severity, received by nerve ending in the abdominal and pelvic region.... --- Walk 2 --- [MG3Z] Pain, unspecified --PARENT--> [?] Pain --CHILD--> [MG30] Chronic pain Def: Pain is an unpleasant sensory and emotional experience associated with, or resembling that associated with, actual or potential tissue damage. Chronic pain is pain that persists or recurs for longer t... --- Walk 3 --- [8E43.Z] Pain disorders, unspecified --PARENT--> [8E43] Pain disorders --CHILD--> [8E43.0] Neuropathic pain Def: Neuropathic pain is described as electric, burning, or shock like, caused by metabolic, nutritional, infectious, genetic, autoimmune, and/or vasculitic processes. The pain may occur spontaneously, wit... --- Walk 4 --- [8E43.Z] Pain disorders, unspecified --PARENT--> [8E43] Pain disorders --CHILD--> [8E43.0] Neuropathic pain Def: Neuropathic pain is described as electric, burning, or shock like, caused by metabolic, nutritional, infectious, genetic, autoimmune, and/or vasculitic processes. The pain may occur spontaneously, wit... --- Walk 5 --- [MG31.Z] Acute pain, unspecified --PARENT--> [MG31] Acute pain Def: Pain with a duration of less than 3 months. This code should be used only when there is no further specification of site.... --CHILD--> [MG31.1] Acute headache, not elsewhere classified --- Walk 6 --- [MG31.Z] Acute pain, unspecified --PARENT--> [MG31] Acute pain Def: Pain with a duration of less than 3 months. This code should be used only when there is no further specification of site.... --CHILD--> [MG31.0] Acute pain in the face, not elsewhere classified
[ "[MG3Z] Pain, unspecified\n --PARENT--> [?] Pain\n --EXCLUDES--> [?] Abdominal or pelvic pain\n Def: Pain, an unpleasant distress sensation occurring in varying degrees of severity, received by nerve ending in the abdominal and pelvic region....", "[MG3Z] Pain, unspecified\n --PARENT--> [?] Pain\n --CHILD--> [MG30] Chronic pain\n Def: Pain is an unpleasant sensory and emotional experience associated with, or resembling that associated with, actual or potential tissue damage. Chronic pain is pain that persists or recurs for longer t...", "[8E43.Z] Pain disorders, unspecified\n --PARENT--> [8E43] Pain disorders\n --CHILD--> [8E43.0] Neuropathic pain\n Def: Neuropathic pain is described as electric, burning, or shock like, caused by metabolic, nutritional, infectious, genetic, autoimmune, and/or vasculitic processes. The pain may occur spontaneously, wit...", "[8E43.Z] Pain disorders, unspecified\n --PARENT--> [8E43] Pain disorders\n --CHILD--> [8E43.0] Neuropathic pain\n Def: Neuropathic pain is described as electric, burning, or shock like, caused by metabolic, nutritional, infectious, genetic, autoimmune, and/or vasculitic processes. The pain may occur spontaneously, wit...", "[MG31.Z] Acute pain, unspecified\n --PARENT--> [MG31] Acute pain\n Def: Pain with a duration of less than 3 months.\n\nThis code should be used only when there is no further specification of site....\n --CHILD--> [MG31.1] Acute headache, not elsewhere classified", "[MG31.Z] Acute pain, unspecified\n --PARENT--> [MG31] Acute pain\n Def: Pain with a duration of less than 3 months.\n\nThis code should be used only when there is no further specification of site....\n --CHILD--> [MG31.0] Acute pain in the face, not elsewhere classified" ]
MG3Z
Pain, unspecified
[ { "from_icd11": "MG3Z", "icd10_code": "R52", "icd10_title": "Pain, unspecified" }, { "from_icd11": "MG3Z", "icd10_code": "R529", "icd10_title": "" }, { "from_icd11": "MG31.Z", "icd10_code": "R520", "icd10_title": "" }, { "from_icd11": "MG30.Z", "icd10_code": "R521", "icd10_title": "" }, { "from_icd11": "MG30.Z", "icd10_code": "R522", "icd10_title": "" }, { "from_icd11": "FB56.2", "icd10_code": "M7918", "icd10_title": "Myalgia, other site" }, { "from_icd11": "FB56.2", "icd10_code": "M7910", "icd10_title": "Myalgia, unspecified site" }, { "from_icd11": "FB56.2", "icd10_code": "M7912", "icd10_title": "Myalgia of auxiliary muscles, head and neck" }, { "from_icd11": "FB56.2", "icd10_code": "M791", "icd10_title": "Myalgia" }, { "from_icd11": "MB25.02", "icd10_code": "R4689", "icd10_title": "Other symptoms and signs involving appearance and behavior" }, { "from_icd11": "MB25.02", "icd10_code": "R4681", "icd10_title": "Obsessive-compulsive behavior" }, { "from_icd11": "MB25.02", "icd10_code": "R468", "icd10_title": "Other symptoms and signs involving appearance and behavior" }, { "from_icd11": "LD2F.11", "icd10_code": "Q872", "icd10_title": "Congenital malformation syndromes predominantly involving limbs" }, { "from_icd11": "5A61.0", "icd10_code": "E230", "icd10_title": "Hypopituitarism" }, { "from_icd11": "5A61.0", "icd10_code": "Q044", "icd10_title": "Septo-optic dysplasia of brain" } ]
R52
Pain, unspecified
Following this reprocessing and reanalysis, the bioinformatics and clinical genetics teams reviewed candidate variants in gene.iobio . One of the candidate variants was a rare de novo frameshift variant in ARID1B. This variant was prioritized at the top of the variant list panel in gene.iobio . Coffin Siris syndrome was part of the initial differential diagnosis for this patient, but the patient did not present with classic Coffin-Siris syndrome. With this consideration, the clinical team entered Coffin Siris syndrome into the phenotype entry component of gene.iobio , which uses Phenolyzer 23 to generate a list of phenotype-associated genes . ARID1B was among the genes in this Coffin Siris syndrome-associated gene list . Also within this view of gene.iobio , the clinical team reviewed key variant annotations such as consequence, gnomAD allele frequency and inheritance . The clinical team also reviewed OMIM phenotypes and PubMed publications related to ARID1B for further clinical evidence. After reviewing this variant, phenotype and literature evidence, the clinical and bioinformatics teams were able to conclude this variant was causative of the patient’s phenotype, as it fits within a larger group of ARID1B-related disorders, of which Coffin-Siris is within 40 . Lastly, the team assigned a significance to the ARID1B variant and entered a note describing why this variant was considered causative .
4.113281
0.486328
sec[2]/p[2]
en
0.999996
34645894
https://doi.org/10.1038/s41598-021-99752-5
[ "this", "variant", "gene", "coffin", "siris", "iobio", "team", "phenotype", "reviewed", "list" ]
[ { "code": "4A01.03", "title": "Transient hypogammaglobulinaemia of infancy" }, { "code": "4A00.0Y", "title": "Other specified functional neutrophil defects" }, { "code": "8A40.Y", "title": "Other specified multiple sclerosis" }, { "code": "8E4A.0", "title": "Paraneoplastic or autoimmune disorders of the central nervous system, brain or spinal cord" }, { "code": "8E01.2", "title": "Variant Creutzfeldt-Jakob Disease" }, { "code": "5C56.00", "title": "Gangliosidosis" }, { "code": "9A70.Y", "title": "Other specified hereditary corneal dystrophies" }, { "code": "GB81", "title": "Autosomal dominant polycystic kidney disease" }, { "code": "8A02.12", "title": "Dystonia associated with heredodegenerative disorders" }, { "code": "5C50.E0", "title": "Classical organic aciduria" } ]
=== ICD-11 CODES FOUND === [4A01.03] Transient hypogammaglobulinaemia of infancy Also known as: Transient hypogammaglobulinaemia of infancy | immunoglobulin maturational delay | THI - [transient hypogammaglobulinaemia of infancy] [4A00.0Y] Other specified functional neutrophil defects Also known as: Other specified functional neutrophil defects | Chronic granulomatous disease | Chronic septic granulomatosis | CGD - [chronic granulomatous disease] | chronic granulomatous disorder [8A40.Y] Other specified multiple sclerosis Also known as: Other specified multiple sclerosis | Certain specified rare variants of multiple sclerosis | Multiple sclerosis, Marburg variant | Myelinoclastic diffuse sclerosis | Schilder disease [8E4A.0] Paraneoplastic or autoimmune disorders of the central nervous system, brain or spinal cord Definition: Paraneoplastic and autoimmune disorders of the central nervous system, brain and spinal cord nervous system result from a targeted immune attack on neurons or glial cells in the central (e.g. encephalopathy, ataxia, myelopathy, myelitis) nervous system. In the paraneoplastic context, this attack is a consequence of a potentially effective tumour immune response initiated by onco-neural antigens derived from a systemic cancer. In the non-paraneoplastic context termed ‘autoimmune’ the etiology rem Also known as: Paraneoplastic or autoimmune disorders of the central nervous system, brain or spinal cord | Paraneoplastic encephalitis | Paraneoplastic encephalitis, neural autoantibody positive | Paraneoplastic encephalitis, neural autoantibody negative | Autoimmune encephalitis [8E01.2] Variant Creutzfeldt-Jakob Disease Definition: A disease of the brain, that is suspected to be caused by a prion associated with Bovine Spongiform Encephalopathy. This disease is characterised by a long incubation period, psychiatric symptoms followed by neurological deficits, and is fatal. Transmission may be by ingestion of food (with a bovine origin) contaminated with infected brain or spinal cord from an infected cow, or blood transfusion. Confirmation is by pathological examination of the brain. Also known as: Variant Creutzfeldt-Jakob Disease | vCJD - [Variant Creutzfeldt-Jakob Disease] [5C56.00] Gangliosidosis Also known as: Gangliosidosis | GM1 gangliosidosis | Landing disease | GM1 gangliosidosis type 1 | Generalised gangliosidosis [9A70.Y] Other specified hereditary corneal dystrophies Also known as: Other specified hereditary corneal dystrophies | Epithelial juvenile corneal dystrophy | TGFBI - [transforming growth factor beta-induced] gene | Granular corneal dystrophy | granular-lattice corneal dystrophy Includes: Granular corneal dystrophy [GB81] Autosomal dominant polycystic kidney disease Definition: Multiple cysts in both kidneys increasing in number and size from adolescence, associated with development of hypertension and chronic renal failure. Autosomal dominant familial pattern is usual and due to mutations on chromosomes 16 and 4. Non-renal manifestations can include cysts in the liver and less commonly pancreas. Cerebral arterial aneurysms with subarachnoid haemorrhage, and other non-renal vascular abnormalities can also occur. Also known as: Autosomal dominant polycystic kidney disease | adult polycystic kidney disease | Polycystic kidney, adult type | APCKD - [autosomal polycystic kidney disease] | Autosomal dominant polycystic kidney disease type 1 without tuberous sclerosis [8A02.12] Dystonia associated with heredodegenerative disorders Definition: Dystonia occurring as a part of a more complex heredodegenerative disorder. It is not a pure dystonia and other neurological findings such as ataxia, pyramidal signs and cognitive issues may be seen. Also known as: Dystonia associated with heredodegenerative disorders | Dystonia due to autosomal dominant disorders | Rapid-onset dystonia-parkinsonism | Dystonia due to dentatorubropallidoluysian atrophy | Dystonia due to Huntington disease [5C50.E0] Classical organic aciduria Definition: This a term used to classify a group of metabolic disorders which disrupt normal amino acid metabolism, particularly branched-chain amino acids, causing a buildup of acids which are usually not present. Also known as: Classical organic aciduria | Methylmalonic aciduria - homocystinuria | Methylmalonic acidaemia - homocystinuria | Methylmalonic aciduria - homocystinuria type cbl C | Methylmalonic acidaemia - homocystinuria type cbl C === GRAPH WALKS === --- Walk 1 --- [4A01.03] Transient hypogammaglobulinaemia of infancy --PARENT--> [4A01.0] Immunodeficiencies with predominantly antibody defects Def: A disorder characterised by an inability to mount a normal immune response due to antibody (i.e. immunoglobulin) defects... --CHILD--> [4A01.01] Immunodeficiencies with severe reduction in at least two serum immunoglobulin isotypes with normal or low numbers of B cells Def: This refers to a nonfamilial type of primary immune deficiency disease characterised by a reduction in at least two serum immunoglobulin isotypes. Circulating B cells may be normal or low.... --- Walk 2 --- [4A01.03] Transient hypogammaglobulinaemia of infancy --PARENT--> [4A01.0] Immunodeficiencies with predominantly antibody defects Def: A disorder characterised by an inability to mount a normal immune response due to antibody (i.e. immunoglobulin) defects... --CHILD--> [4A01.02] Specific antibody deficiency with normal immunoglobulin concentrations or normal number of B cells --- Walk 3 --- [4A00.0Y] Other specified functional neutrophil defects --PARENT--> [4A00.0] Functional neutrophil defects --RELATED_TO--> [?] Papillon-Lefèvre syndrome Def: Papillon-Lefèvre syndrome (PLS) is a rare autosomal recessive disorder characterised by palmoplantar hyperkeratosis and severe early onset of destructive periodontitis leading to premature loss of bot... --- Walk 4 --- [4A00.0Y] Other specified functional neutrophil defects --PARENT--> [4A00.0] Functional neutrophil defects --CHILD--> [4A00.00] Neutrophil immunodeficiency syndrome Def: Neutrophil immunodeficiency syndrome is a primary immunodeficiency characterised by neutrophilia with severe neutrophil dysfunction, leukocytosis, a predisposition to bacterial infections and poor wou... --- Walk 5 --- [8A40.Y] Other specified multiple sclerosis --PARENT--> [8A40] Multiple sclerosis Def: Multiple Sclerosis (MS) is a chronic, inflammatory demyelinating disease of the central nervous system. Three categories of multiple sclerosis have been outlined: Relapsing/remitting, secondary progre... --PARENT--> [?] Multiple sclerosis or other white matter disorders Def: This is a group of conditions involving demyelination, damage to the myelin sheath which protects nerve axons and is responsible for neurotransmission.... --- Walk 6 --- [8A40.Y] Other specified multiple sclerosis --PARENT--> [8A40] Multiple sclerosis Def: Multiple Sclerosis (MS) is a chronic, inflammatory demyelinating disease of the central nervous system. Three categories of multiple sclerosis have been outlined: Relapsing/remitting, secondary progre... --CHILD--> [8A40.2] Secondary progressive multiple sclerosis
[ "[4A01.03] Transient hypogammaglobulinaemia of infancy\n --PARENT--> [4A01.0] Immunodeficiencies with predominantly antibody defects\n Def: A disorder characterised by an inability to mount a normal immune response due to antibody (i.e. immunoglobulin) defects...\n --CHILD--> [4A01.01] Immunodeficiencies with severe reduction in at least two serum immunoglobulin isotypes with normal or low numbers of B cells\n Def: This refers to a nonfamilial type of primary immune deficiency disease characterised by a reduction in at least two serum immunoglobulin isotypes. Circulating B cells may be normal or low....", "[4A01.03] Transient hypogammaglobulinaemia of infancy\n --PARENT--> [4A01.0] Immunodeficiencies with predominantly antibody defects\n Def: A disorder characterised by an inability to mount a normal immune response due to antibody (i.e. immunoglobulin) defects...\n --CHILD--> [4A01.02] Specific antibody deficiency with normal immunoglobulin concentrations or normal number of B cells", "[4A00.0Y] Other specified functional neutrophil defects\n --PARENT--> [4A00.0] Functional neutrophil defects\n --RELATED_TO--> [?] Papillon-Lefèvre syndrome\n Def: Papillon-Lefèvre syndrome (PLS) is a rare autosomal recessive disorder characterised by palmoplantar hyperkeratosis and severe early onset of destructive periodontitis leading to premature loss of bot...", "[4A00.0Y] Other specified functional neutrophil defects\n --PARENT--> [4A00.0] Functional neutrophil defects\n --CHILD--> [4A00.00] Neutrophil immunodeficiency syndrome\n Def: Neutrophil immunodeficiency syndrome is a primary immunodeficiency characterised by neutrophilia with severe neutrophil dysfunction, leukocytosis, a predisposition to bacterial infections and poor wou...", "[8A40.Y] Other specified multiple sclerosis\n --PARENT--> [8A40] Multiple sclerosis\n Def: Multiple Sclerosis (MS) is a chronic, inflammatory demyelinating disease of the central nervous system. Three categories of multiple sclerosis have been outlined: Relapsing/remitting, secondary progre...\n --PARENT--> [?] Multiple sclerosis or other white matter disorders\n Def: This is a group of conditions involving demyelination, damage to the myelin sheath which protects nerve axons and is responsible for neurotransmission....", "[8A40.Y] Other specified multiple sclerosis\n --PARENT--> [8A40] Multiple sclerosis\n Def: Multiple Sclerosis (MS) is a chronic, inflammatory demyelinating disease of the central nervous system. Three categories of multiple sclerosis have been outlined: Relapsing/remitting, secondary progre...\n --CHILD--> [8A40.2] Secondary progressive multiple sclerosis" ]
4A01.03
Transient hypogammaglobulinaemia of infancy
[ { "from_icd11": "4A01.03", "icd10_code": "D807", "icd10_title": "Transient hypogammaglobulinemia of infancy" }, { "from_icd11": "8E4A.0", "icd10_code": "G3183", "icd10_title": "Dementia with Lewy bodies" }, { "from_icd11": "8E4A.0", "icd10_code": "G2581", "icd10_title": "Restless legs syndrome" }, { "from_icd11": "8E4A.0", "icd10_code": "G3184", "icd10_title": "Mild cognitive impairment, so stated" }, { "from_icd11": "8E4A.0", "icd10_code": "G9349", "icd10_title": "Other encephalopathy" }, { "from_icd11": "8E4A.0", "icd10_code": "G0481", "icd10_title": "Other encephalitis and encephalomyelitis" }, { "from_icd11": "8E4A.0", "icd10_code": "G9589", "icd10_title": "Other specified diseases of spinal cord" }, { "from_icd11": "8E4A.0", "icd10_code": "G2589", "icd10_title": "Other specified extrapyramidal and movement disorders" }, { "from_icd11": "8E4A.0", "icd10_code": "G3189", "icd10_title": "Other specified degenerative diseases of nervous system" }, { "from_icd11": "8E4A.0", "icd10_code": "G2582", "icd10_title": "Stiff-man syndrome" }, { "from_icd11": "8E4A.0", "icd10_code": "G0489", "icd10_title": "Other myelitis" }, { "from_icd11": "8E4A.0", "icd10_code": "G9581", "icd10_title": "Conus medullaris syndrome" }, { "from_icd11": "8E4A.0", "icd10_code": "G3185", "icd10_title": "Corticobasal degeneration" }, { "from_icd11": "8E4A.0", "icd10_code": "G3181", "icd10_title": "Alpers disease" }, { "from_icd11": "8E4A.0", "icd10_code": "G3182", "icd10_title": "Leigh's disease" } ]
D807
Transient hypogammaglobulinemia of infancy
Our reported case was solitary SEM of prostate cancer of the small cell type. The majority of prostate cancers are acinar adenocarcinomas. Histological variants of prostate cancers can be defined as acinar adenocarcinoma and nonacinar carcinoma variants. The nonacinar carcinoma variants account for approximately 5–10% of the carcinomas that occur in the prostate. These include sarcomatoid carcinoma, ductal adenocarcinoma, urothelial carcinoma, basal cell carcinoma, and small cell carcinoma, in other words, neuroendocrine tumors. Small cell carcinoma developing in the prostate is a rare and very aggressive tumor, which frequently presents with disseminated disease. The incidence of prostate small cell carcinoma ranges from 0.3% to 1.0% in all prostate cancers. Prostatic small cell carcinoma shows different clinical features from those of prostatic acinar adenocarcinoma. Distinguishing clinical features include a lower percentage of men who present with an elevated serum PSA level at advanced stages of prostate cancer, poor hormonal responsiveness, and a short patient survival time. Most patients are 65–72 years old, and the most frequent presenting symptoms arise from bladder outlet obstruction and disseminated disease. One-third to two-thirds of patients with prostatic small cell carcinoma show an elevated serum PSA level, which could be due to an admixed adenocarcinomatous component [ 11 – 13 ].
4.257813
0.643066
sec[2]/p[4]
en
0.999996
27413569
https://doi.org/10.1155/2016/4728343
[ "carcinoma", "prostate", "cell", "small", "cancers", "acinar", "variants", "adenocarcinoma", "prostatic", "cancer" ]
[ { "code": "2D41", "title": "Unspecified carcinoma of unspecified site" }, { "code": "2C3Y", "title": "Other specified malignant neoplasms of skin" }, { "code": "2E6Z", "title": "Carcinoma in situ of unspecified site" }, { "code": "2C25.5", "title": "Unspecified malignant epithelial neoplasm of bronchus or lung" }, { "code": "2C90.Y", "title": "Other specified malignant neoplasms of kidney, except renal pelvis" }, { "code": "GA90", "title": "Hyperplasia of prostate" }, { "code": "GA91.Z", "title": "Inflammatory or other diseases of prostate, unspecified" }, { "code": "GA91.Y", "title": "Other specified inflammatory or other diseases of prostate" }, { "code": "GA91.0", "title": "Chronic prostatitis" }, { "code": "MF40.1", "title": "Problems of the prostate" } ]
=== ICD-11 CODES FOUND === [2D41] Unspecified carcinoma of unspecified site Also known as: Unspecified carcinoma of unspecified site | carcinoma of unspecified primary site | carcinoma NOS | Carcinoma in polyp of unspecified site | Carcinoma with apocrine metaplasia of unspecified site [2C3Y] Other specified malignant neoplasms of skin Also known as: Other specified malignant neoplasms of skin | Malignant neoplasm of eyelid NOS | Malignant pilonidal cyst | Radiotherapy-induced skin malignancy | Cutaneous carcinoma [2E6Z] Carcinoma in situ of unspecified site Also known as: Carcinoma in situ of unspecified site | carcinoma in situ of unspecified site | carcinoma in situ NOS | carcinoma in situ | in situ neoplasm [2C25.5] Unspecified malignant epithelial neoplasm of bronchus or lung Also known as: Unspecified malignant epithelial neoplasm of bronchus or lung | unspecified carcinoma of bronchus or lung | Metastatic lung carcinoma [primary lung carcinoma spreading elsewhere] | Metastatic carcinoma of lung [primary carcinoma of lung spreading elsewhere] | Lung carcinoma [2C90.Y] Other specified malignant neoplasms of kidney, except renal pelvis Also known as: Other specified malignant neoplasms of kidney, except renal pelvis | Congenital mesoblastic nephroma | Nephroblastoma | Wilms tumour of kidney | Wilms tumour of unspecified site Includes: Nephroblastoma [GA90] Hyperplasia of prostate Definition: A condition of the prostate, caused by an increased rate of cellular division of the glandular and stromal cells. This condition is characterised by enlargement of the prostatic tissue, dysuria, urinary urgency, nocturia, weak urine stream, straining while urinating, incomplete bladder emptying during urination, or increased frequency of urinary tract infection. Also known as: Hyperplasia of prostate | Adenofibromatous hypertrophy of prostate | benign prostatic hyperplasia | prostate hyperplasia | prostatic area hypertrophy Includes: Adenofibromatous hypertrophy of prostate Excludes: Benign neoplasms of prostate [GA91.Z] Inflammatory or other diseases of prostate, unspecified Also known as: Inflammatory or other diseases of prostate, unspecified | Inflammatory or other diseases of prostate | inflammation of prostate NOS | prostatitis NOS | disease of prostate NOS [GA91.Y] Other specified inflammatory or other diseases of prostate Also known as: Other specified inflammatory or other diseases of prostate | Acute bacterial prostatitis | acute prostatitis | Prostatitis category I (NIH classification) | Prostatitis category I [GA91.0] Chronic prostatitis Definition: A condition caused by obstruction of the prostate glands. This condition is characterised by inflammation of the prostate gland, dysuria, pollakiuria, urinary urgency, genital pain, lower back pain, abdominal pain, and repeated bladder infections that last for at least three months. Also known as: Chronic prostatitis | Fibrous prostatitis | Hypertrophic prostatitis | Subacute prostatitis | Chronic bacterial prostatitis [MF40.1] Problems of the prostate Definition: A group of disorders associated with the prostate occurring in diseases more specifically classified elsewhere. Also known as: Problems of the prostate === GRAPH WALKS === --- Walk 1 --- [2D41] Unspecified carcinoma of unspecified site --PARENT--> [?] Malignant neoplasms of ill-defined or unspecified primary sites --CHILD--> [2D42] Malignant neoplasms of ill-defined sites Def: Malignant neoplasms of ill defined sites is used for cases where the documentation refers to a site that includes multiple organ systems and tissue types that should be coded separately.... --- Walk 2 --- [2D41] Unspecified carcinoma of unspecified site --PARENT--> [?] Malignant neoplasms of ill-defined or unspecified primary sites --CHILD--> [2D40] Adenocarcinoma of unspecified site Def: A common cancer characterised by the presence of malignant glandular cells. Morphologically, adenocarcinomas are classified according to the growth pattern (e.g., papillary, alveolar) or according to ... --- Walk 3 --- [2C3Y] Other specified malignant neoplasms of skin --PARENT--> [?] Malignant neoplasms of skin Def: A primary or metastatic tumour involving the skin. Primary malignant skin tumours most often are carcinomas (either basal cell or squamous cell carcinomas that arise from cells in the epidermis) or me... --PARENT--> [?] Malignant neoplasms, stated or presumed to be primary, of specified sites, except of lymphoid, haematopoietic, central nervous system or related tissues --- Walk 4 --- [2C3Y] Other specified malignant neoplasms of skin --PARENT--> [?] Malignant neoplasms of skin Def: A primary or metastatic tumour involving the skin. Primary malignant skin tumours most often are carcinomas (either basal cell or squamous cell carcinomas that arise from cells in the epidermis) or me... --EXCLUDES--> [?] Malignant mesenchymal neoplasms Def: A usually aggressive malignant mesenchymal cell tumour most commonly arising from muscle, fat, fibrous tissue, bone, cartilage, and blood vessels. Sarcomas occur in both children and adults. The progn... --- Walk 5 --- [2E6Z] Carcinoma in situ of unspecified site --PARENT--> [?] In situ neoplasms, except of lymphoid, haematopoietic, central nervous system or related tissues --CHILD--> [2E60] Carcinoma in situ of oral cavity, oesophagus or stomach --- Walk 6 --- [2E6Z] Carcinoma in situ of unspecified site --PARENT--> [?] In situ neoplasms, except of lymphoid, haematopoietic, central nervous system or related tissues --CHILD--> [2E61] Carcinoma in situ of other or unspecified digestive organs
[ "[2D41] Unspecified carcinoma of unspecified site\n --PARENT--> [?] Malignant neoplasms of ill-defined or unspecified primary sites\n --CHILD--> [2D42] Malignant neoplasms of ill-defined sites\n Def: Malignant neoplasms of ill defined sites is used for cases where the documentation refers to a site that includes multiple organ systems and tissue types that should be coded separately....", "[2D41] Unspecified carcinoma of unspecified site\n --PARENT--> [?] Malignant neoplasms of ill-defined or unspecified primary sites\n --CHILD--> [2D40] Adenocarcinoma of unspecified site\n Def: A common cancer characterised by the presence of malignant glandular cells. Morphologically, adenocarcinomas are classified according to the growth pattern (e.g., papillary, alveolar) or according to ...", "[2C3Y] Other specified malignant neoplasms of skin\n --PARENT--> [?] Malignant neoplasms of skin\n Def: A primary or metastatic tumour involving the skin. Primary malignant skin tumours most often are carcinomas (either basal cell or squamous cell carcinomas that arise from cells in the epidermis) or me...\n --PARENT--> [?] Malignant neoplasms, stated or presumed to be primary, of specified sites, except of lymphoid, haematopoietic, central nervous system or related tissues", "[2C3Y] Other specified malignant neoplasms of skin\n --PARENT--> [?] Malignant neoplasms of skin\n Def: A primary or metastatic tumour involving the skin. Primary malignant skin tumours most often are carcinomas (either basal cell or squamous cell carcinomas that arise from cells in the epidermis) or me...\n --EXCLUDES--> [?] Malignant mesenchymal neoplasms\n Def: A usually aggressive malignant mesenchymal cell tumour most commonly arising from muscle, fat, fibrous tissue, bone, cartilage, and blood vessels. Sarcomas occur in both children and adults. The progn...", "[2E6Z] Carcinoma in situ of unspecified site\n --PARENT--> [?] In situ neoplasms, except of lymphoid, haematopoietic, central nervous system or related tissues\n --CHILD--> [2E60] Carcinoma in situ of oral cavity, oesophagus or stomach", "[2E6Z] Carcinoma in situ of unspecified site\n --PARENT--> [?] In situ neoplasms, except of lymphoid, haematopoietic, central nervous system or related tissues\n --CHILD--> [2E61] Carcinoma in situ of other or unspecified digestive organs" ]
2D41
Unspecified carcinoma of unspecified site
[ { "from_icd11": "2E6Z", "icd10_code": "D098", "icd10_title": "Carcinoma in situ of other specified sites" }, { "from_icd11": "2E6Z", "icd10_code": "D099", "icd10_title": "Carcinoma in situ, unspecified" }, { "from_icd11": "2E6Z", "icd10_code": "D00-D09", "icd10_title": "" }, { "from_icd11": "2E6Z", "icd10_code": "D09", "icd10_title": "Carcinoma in situ of other and unspecified sites" }, { "from_icd11": "2E6Z", "icd10_code": "D097", "icd10_title": "" }, { "from_icd11": "GA90", "icd10_code": "N402", "icd10_title": "Nodular prostate without lower urinary tract symptoms" }, { "from_icd11": "GA90", "icd10_code": "N403", "icd10_title": "Nodular prostate with lower urinary tract symptoms" }, { "from_icd11": "GA90", "icd10_code": "N400", "icd10_title": "Benign prostatic hyperplasia without lower urinary tract symptoms" }, { "from_icd11": "GA90", "icd10_code": "N401", "icd10_title": "Benign prostatic hyperplasia with lower urinary tract symptoms" }, { "from_icd11": "GA90", "icd10_code": "N40", "icd10_title": "Benign prostatic hyperplasia" }, { "from_icd11": "GA91.Z", "icd10_code": "N414", "icd10_title": "Granulomatous prostatitis" }, { "from_icd11": "GA91.Z", "icd10_code": "N4289", "icd10_title": "Other specified disorders of prostate" }, { "from_icd11": "GA91.Z", "icd10_code": "N4283", "icd10_title": "Cyst of prostate" }, { "from_icd11": "GA91.Z", "icd10_code": "N410", "icd10_title": "Acute prostatitis" }, { "from_icd11": "GA91.Z", "icd10_code": "N419", "icd10_title": "Inflammatory disease of prostate, unspecified" } ]
D098
Carcinoma in situ of other specified sites
In the preoperative period after BPGP measures were implemented, patients were also evaluated based on their comorbidities; hemoglobin was raised above 12 g/dL with iron and erythropoietin when needed. Autologous blood donation was suspended as previous patients all had a significant decrease in hemoglobin preoperatively after donating blood. A preoperative bath was implemented with chlorohexidine both the day before surgery and the day of surgery. Alcohol-based chlorohexidine was introduced for skin prep at the time of surgery, and a time-out with a checklist was implemented. Anesthesiology introduced tranexamic acid in a dose varying between 10–30 mg/kg initially, followed by 3 to 5 mg/kg/h of perfusion. Progressive remifentanil infusion replaced the use of fentanyl during anesthesia. Stainless steel instrumentation was abandoned and replaced by titanium-with-cobalt chrome rods; posterior osteotomies in the curve apex became routine. Hybrid constructs were already being replaced by all-screw constructs with higher implant density due to surgeons’ increased familiarity with thoracic pedicle screws. Multimodal neuromonitoring was introduced, replacing somatosensory-only monitoring. In the postoperative period, a restrictive transfusion policy was initiated, thus avoiding transfusion when hemoglobin was above 7 g/dL following an uneventful surgery with no clinical signs of hemodynamic instability.
4.027344
0.463379
sec[1]/sec[0]/p[0]
en
0.999998
PMC10252400
https://doi.org/10.3390/healthcare11111566
[ "implemented", "hemoglobin", "introduced", "replaced", "preoperative", "period", "patients", "based", "blood", "chlorohexidine" ]
[ { "code": "3A51.1", "title": "Sickle cell disease without crisis" }, { "code": "3A51.Z", "title": "Sickle cell disorders or other haemoglobinopathies, unspecified" }, { "code": "MA18.4", "title": "Low haemoglobin" }, { "code": "3A50.4", "title": "Hereditary persistence of fetal haemoglobin" }, { "code": "3A51.A", "title": "Haemoglobin E disease" }, { "code": "PL14.1", "title": "Non provision of necessary procedure" }, { "code": "QB51.1", "title": "Presence of urogenital implants" }, { "code": "QB63.5", "title": "Presence of transplanted bone" }, { "code": "LD7Y", "title": "Other specified chromosomal anomalies, excluding gene mutations" }, { "code": "QB63.Z", "title": "Presence of transplanted organ or tissue, unspecified" } ]
=== ICD-11 CODES FOUND === [3A51.1] Sickle cell disease without crisis Definition: A disorder caused by a HbS mutation in the haemoglobin gene. This disorder is characterised by abnormal rigid sickle-shaped red blood cells decreasing its ability to carry oxygen. This disorder may present with fatigue, shortness of breath, dizziness, headaches, pallor of skin or mucous membranes, and jaundice. This disorder is confirmed by identification of HbS mutation by genetic testing. Also known as: Sickle cell disease without crisis | Hb-SS disease without crisis | HbSS without crisis | Sickle-cell anaemia without crisis | SCD - [sickle cell disease] [3A51.Z] Sickle cell disorders or other haemoglobinopathies, unspecified Also known as: Sickle cell disorders or other haemoglobinopathies, unspecified | Sickle cell disorders or other haemoglobinopathies | Sickle-cell disease or disorder with elliptocytosis | sickle-cell hemoglobin disease with elliptocytosis | sickle-cell elliptocytosis [MA18.4] Low haemoglobin Also known as: Low haemoglobin Excludes: Low affinity haemoglobin [3A50.4] Hereditary persistence of fetal haemoglobin Definition: Hereditary persistence of fetal haemoglobin (HPFH) associated with beta-thalassaemia is a haemoglobinopathy characterised by high haemoglobin (Hb)F levels and an increased number of fetal-Hb-containing cells. The association of HPFH with beta-thalassaemia mitigates the clinical manifestations which vary from a normal state to beta-thalassaemia intermedia. Also known as: Hereditary persistence of fetal haemoglobin | HPFH - [Hereditary persistence of fetal haemoglobin] | fetal haemoglobin | persistence of fetal haemoglobin | persistent haemoglobin F [3A51.A] Haemoglobin E disease Definition: Haemoglobin E disease is characterised by the synthesis of an abnormal haemoglobin called haemoglobin E (HbE), instead of the normal haemoglobin A (HbA). Subjects heterozygous for HbE (AE) have an asymptomatic condition with no clinical relevance, except for the risk of transmitting E/beta thalassemia if the other parent carries beta thalassemia. The severity of these E/beta thalassemia forms is very variable, the clinical picture ranging from that of beta thalassemia minor through to thalassemi Also known as: Haemoglobin E disease | Homozygous HbE carriers | Compound HbE or other Hb mutant heterozygotes [PL14.1] Non provision of necessary procedure Also known as: Non provision of necessary procedure | Nonadministration of surgical and medical care | injury due to nonadministration of surgical and medical care | Premature cessation of surgical and medical care | Failure to introduce or to remove other tube or instrument Excludes: Delayed treatment [QB51.1] Presence of urogenital implants Also known as: Presence of urogenital implants | Presence of bladder implant | bladder replaced by other means | replacement of bladder by artificial or mechanical device or prosthesis | Presence of urethral stent [QB63.5] Presence of transplanted bone Also known as: Presence of transplanted bone | bone replaced by transplant | bone transplant status [LD7Y] Other specified chromosomal anomalies, excluding gene mutations Also known as: Other specified chromosomal anomalies, excluding gene mutations | Tetrasomies of the autosomes | Tetrasomy 12p mosaicism | Pallister-Killian syndrome | Tetrasomy 15q [QB63.Z] Presence of transplanted organ or tissue, unspecified Also known as: Presence of transplanted organ or tissue, unspecified | Presence of transplanted organ or tissue | transplanted organ or tissue status | organ or tissue replaced by heterogenous or homogenous transplant | organ transplant === GRAPH WALKS === --- Walk 1 --- [3A51.1] Sickle cell disease without crisis Def: A disorder caused by a HbS mutation in the haemoglobin gene. This disorder is characterised by abnormal rigid sickle-shaped red blood cells decreasing its ability to carry oxygen. This disorder may pr... --PARENT--> [3A51] Sickle cell disorders or other haemoglobinopathies Def: Any disorder caused by a HbS mutation in the haemoglobin gene. This disorder is characterised by abnormal rigid sickle-shaped red blood cells decreasing its ability to carry oxygen. This disorder may ... --RELATED_TO--> [?] Other sickle-cell disorders with retinopathy Def: This is an autosomal recessive genetic blood disorder with overdominance, characterised by red blood cells that assume an abnormal, rigid, sickle shape. This diagnosis is due to persistent or acute da... --- Walk 2 --- [3A51.1] Sickle cell disease without crisis Def: A disorder caused by a HbS mutation in the haemoglobin gene. This disorder is characterised by abnormal rigid sickle-shaped red blood cells decreasing its ability to carry oxygen. This disorder may pr... --PARENT--> [3A51] Sickle cell disorders or other haemoglobinopathies Def: Any disorder caused by a HbS mutation in the haemoglobin gene. This disorder is characterised by abnormal rigid sickle-shaped red blood cells decreasing its ability to carry oxygen. This disorder may ... --CHILD--> [3A51.0] Sickle cell trait Def: A disease caused by genetic inheritance of one abnormal allele of the haemoglobin gene. This disease does not display the severe symptoms of sickle cell disease that occurs in homozygous individuals. ... --- Walk 3 --- [3A51.Z] Sickle cell disorders or other haemoglobinopathies, unspecified --PARENT--> [3A51] Sickle cell disorders or other haemoglobinopathies Def: Any disorder caused by a HbS mutation in the haemoglobin gene. This disorder is characterised by abnormal rigid sickle-shaped red blood cells decreasing its ability to carry oxygen. This disorder may ... --RELATED_TO--> [?] Other sickle-cell disorders with retinopathy Def: This is an autosomal recessive genetic blood disorder with overdominance, characterised by red blood cells that assume an abnormal, rigid, sickle shape. This diagnosis is due to persistent or acute da... --- Walk 4 --- [3A51.Z] Sickle cell disorders or other haemoglobinopathies, unspecified --PARENT--> [3A51] Sickle cell disorders or other haemoglobinopathies Def: Any disorder caused by a HbS mutation in the haemoglobin gene. This disorder is characterised by abnormal rigid sickle-shaped red blood cells decreasing its ability to carry oxygen. This disorder may ... --CHILD--> [3A51.1] Sickle cell disease without crisis Def: A disorder caused by a HbS mutation in the haemoglobin gene. This disorder is characterised by abnormal rigid sickle-shaped red blood cells decreasing its ability to carry oxygen. This disorder may pr... --- Walk 5 --- [MA18.4] Low haemoglobin --EXCLUDES--> [?] Low affinity haemoglobin Def: A disease caused by determinants arising after birth, in the antenatal period or by genetically inherited factors leading to low oxygen affinity haemoglobin. This disease is characterised by abnormali... --PARENT--> [?] Other haemoglobinopathies Def: Any disease caused by determinants leading to abnormalities the integral structure of the haemoglobin molecule. This disease is characterised by decreased levels of red blood cells in the body. Confir... --- Walk 6 --- [MA18.4] Low haemoglobin --EXCLUDES--> [?] Low affinity haemoglobin Def: A disease caused by determinants arising after birth, in the antenatal period or by genetically inherited factors leading to low oxygen affinity haemoglobin. This disease is characterised by abnormali... --PARENT--> [?] Other haemoglobinopathies Def: Any disease caused by determinants leading to abnormalities the integral structure of the haemoglobin molecule. This disease is characterised by decreased levels of red blood cells in the body. Confir...
[ "[3A51.1] Sickle cell disease without crisis\n Def: A disorder caused by a HbS mutation in the haemoglobin gene. This disorder is characterised by abnormal rigid sickle-shaped red blood cells decreasing its ability to carry oxygen. This disorder may pr...\n --PARENT--> [3A51] Sickle cell disorders or other haemoglobinopathies\n Def: Any disorder caused by a HbS mutation in the haemoglobin gene. This disorder is characterised by abnormal rigid sickle-shaped red blood cells decreasing its ability to carry oxygen. This disorder may ...\n --RELATED_TO--> [?] Other sickle-cell disorders with retinopathy\n Def: This is an autosomal recessive genetic blood disorder with overdominance, characterised by red blood cells that assume an abnormal, rigid, sickle shape. This diagnosis is due to persistent or acute da...", "[3A51.1] Sickle cell disease without crisis\n Def: A disorder caused by a HbS mutation in the haemoglobin gene. This disorder is characterised by abnormal rigid sickle-shaped red blood cells decreasing its ability to carry oxygen. This disorder may pr...\n --PARENT--> [3A51] Sickle cell disorders or other haemoglobinopathies\n Def: Any disorder caused by a HbS mutation in the haemoglobin gene. This disorder is characterised by abnormal rigid sickle-shaped red blood cells decreasing its ability to carry oxygen. This disorder may ...\n --CHILD--> [3A51.0] Sickle cell trait\n Def: A disease caused by genetic inheritance of one abnormal allele of the haemoglobin gene. This disease does not display the severe symptoms of sickle cell disease that occurs in homozygous individuals. ...", "[3A51.Z] Sickle cell disorders or other haemoglobinopathies, unspecified\n --PARENT--> [3A51] Sickle cell disorders or other haemoglobinopathies\n Def: Any disorder caused by a HbS mutation in the haemoglobin gene. This disorder is characterised by abnormal rigid sickle-shaped red blood cells decreasing its ability to carry oxygen. This disorder may ...\n --RELATED_TO--> [?] Other sickle-cell disorders with retinopathy\n Def: This is an autosomal recessive genetic blood disorder with overdominance, characterised by red blood cells that assume an abnormal, rigid, sickle shape. This diagnosis is due to persistent or acute da...", "[3A51.Z] Sickle cell disorders or other haemoglobinopathies, unspecified\n --PARENT--> [3A51] Sickle cell disorders or other haemoglobinopathies\n Def: Any disorder caused by a HbS mutation in the haemoglobin gene. This disorder is characterised by abnormal rigid sickle-shaped red blood cells decreasing its ability to carry oxygen. This disorder may ...\n --CHILD--> [3A51.1] Sickle cell disease without crisis\n Def: A disorder caused by a HbS mutation in the haemoglobin gene. This disorder is characterised by abnormal rigid sickle-shaped red blood cells decreasing its ability to carry oxygen. This disorder may pr...", "[MA18.4] Low haemoglobin\n --EXCLUDES--> [?] Low affinity haemoglobin\n Def: A disease caused by determinants arising after birth, in the antenatal period or by genetically inherited factors leading to low oxygen affinity haemoglobin. This disease is characterised by abnormali...\n --PARENT--> [?] Other haemoglobinopathies\n Def: Any disease caused by determinants leading to abnormalities the integral structure of the haemoglobin molecule. This disease is characterised by decreased levels of red blood cells in the body. Confir...", "[MA18.4] Low haemoglobin\n --EXCLUDES--> [?] Low affinity haemoglobin\n Def: A disease caused by determinants arising after birth, in the antenatal period or by genetically inherited factors leading to low oxygen affinity haemoglobin. This disease is characterised by abnormali...\n --PARENT--> [?] Other haemoglobinopathies\n Def: Any disease caused by determinants leading to abnormalities the integral structure of the haemoglobin molecule. This disease is characterised by decreased levels of red blood cells in the body. Confir..." ]
3A51.1
Sickle cell disease without crisis
[ { "from_icd11": "3A51.1", "icd10_code": "D571", "icd10_title": "Sickle-cell disease without crisis" }, { "from_icd11": "3A51.Z", "icd10_code": "D57411", "icd10_title": "Sickle-cell thalassemia with acute chest syndrome" }, { "from_icd11": "3A51.Z", "icd10_code": "D57412", "icd10_title": "Sickle-cell thalassemia with splenic sequestration" }, { "from_icd11": "3A51.Z", "icd10_code": "D57419", "icd10_title": "Sickle-cell thalassemia with crisis, unspecified" }, { "from_icd11": "3A51.Z", "icd10_code": "D5740", "icd10_title": "Sickle-cell thalassemia without crisis" }, { "from_icd11": "3A51.Z", "icd10_code": "D57819", "icd10_title": "Other sickle-cell disorders with crisis, unspecified" }, { "from_icd11": "3A51.Z", "icd10_code": "D5780", "icd10_title": "Other sickle-cell disorders without crisis" }, { "from_icd11": "3A51.Z", "icd10_code": "D57811", "icd10_title": "Other sickle-cell disorders with acute chest syndrome" }, { "from_icd11": "3A51.Z", "icd10_code": "D57", "icd10_title": "Sickle-cell disorders" }, { "from_icd11": "3A51.Z", "icd10_code": "D578", "icd10_title": "Other sickle-cell disorders" }, { "from_icd11": "3A50.4", "icd10_code": "D564", "icd10_title": "Hereditary persistence of fetal hemoglobin [HPFH]" }, { "from_icd11": "PL14.1", "icd10_code": "Y654", "icd10_title": "Failure to introduce or to remove other tube or instrument" }, { "from_icd11": "PL14.1", "icd10_code": "Y66", "icd10_title": "Nonadministration of surgical and medical care" }, { "from_icd11": "QB51.1", "icd10_code": "Z960", "icd10_title": "Presence of urogenital implants" }, { "from_icd11": "QB63.5", "icd10_code": "Z946", "icd10_title": "Bone transplant status" } ]
D571
Sickle-cell disease without crisis
There are several reasons for performing RARC for multiple recurrent NMIBC without prior TURBT. First, the mortality rate of cystectomy for uncontrolled hemorrhagic cystitis is 16%. 11 Therefore, if there was a high likelihood of uncontrolled bleeding, immediate radical cystectomy would be appealing. Second, this patient did not want TURBT because of pain during bladder irrigation for hemorrhagic cystitis and bleeding after TURBT and chose cystectomy over bladder preservation. A possible serious complication of this surgery is rectal injury. The incidence of anastomotic leakage (25.0% vs 13.7%; p = 0.019) and the requirement for a permanent stoma (41.0% vs 12.4%; p < 0.001) were significantly higher in patients who underwent rectal cancer surgery following prior curative treatment for prostate cancer, compared with those who did not receive any prostatic intervention. 12 There are no reports of radical cystectomy after SRT following radical prostatectomy, but considering the previous reports, it should be recognized that rectal injury is more likely to result in permanent colostomy than routine radical total cystectomy. Therefore, the patient should be informed of the possibility of permanent colostomy before surgery. Significantly, this report acknowledges its limitations as it presents an exceptional case of radical cystectomy, a procedure that deviates from the conventional treatment approach.
4.152344
0.819824
sec[2]/p[1]
en
0.999996
37667760
https://doi.org/10.1002/iju5.12616
[ "cystectomy", "radical", "turbt", "this", "rectal", "permanent", "uncontrolled", "hemorrhagic", "cystitis", "therefore" ]
[ { "code": "QF01.Y", "title": "Other specified acquired absence of organs" }, { "code": "DC14.1", "title": "Postcholecystectomy syndrome" }, { "code": "GC01.0", "title": "Bladder neck obstruction" }, { "code": "4A01.03", "title": "Transient hypogammaglobulinaemia of infancy" }, { "code": "DB30.4", "title": "Stenosis of the rectum" }, { "code": "DB31.0&XA4KU2", "title": "Rectal fistula" }, { "code": "NB91.91", "title": "Laceration of rectum" }, { "code": "2F90.1", "title": "Neoplasms of unknown behaviour of rectum" }, { "code": "DB32.2Z&XA4KU2", "title": "Rectal dilatation" }, { "code": "8E21", "title": "Permanent vegetative state" } ]
=== ICD-11 CODES FOUND === [QF01.Y] Other specified acquired absence of organs Also known as: Other specified acquired absence of organs | Acquired absence of part of head or neck | Acquired absence of eye | absence of eye | absence of eyeball [DC14.1] Postcholecystectomy syndrome Definition: This describes the presence of abdominal symptoms after surgical removal of the gallbladder. Symptoms may include nausea and vomiting, bloating and diarrhoea, and pain in the upper right abdomen. The pain is often ascribed to discoordination of biliary sphincter of Oddi. Also known as: Postcholecystectomy syndrome | post cholecystectomy syndrome [GC01.0] Bladder neck obstruction Definition: A condition of the bladder, caused by congenital or acquired abnormalities that impair the muscles that connect the bladder to the urethra. This condition is characterised by obstruction of the bladder neck and constricted opening during urination. This condition may also present with pelvic pain, pollakiuria, incontinence, or incomplete bladder emptying. Confirmation is by video urodynamics to observe the obstruction as the bladder fills and voids. Also known as: Bladder neck obstruction | bladder outlet obstruction | obstruction of bladder neck or vesicourethral orifice | vesicourethral orifice obstruction | BNO - [bladder neck obstruction] Includes: Acquired bladder neck stenosis [4A01.03] Transient hypogammaglobulinaemia of infancy Also known as: Transient hypogammaglobulinaemia of infancy | immunoglobulin maturational delay | THI - [transient hypogammaglobulinaemia of infancy] [DB30.4] Stenosis of the rectum Definition: Rectal stenosis is defined as narrowing of the rectum. Also known as: Stenosis of the rectum | obstructed rectum | rectal stenosis | stricture of rectum | rectal obstruction [NB91.91] Laceration of rectum Also known as: Laceration of rectum [2F90.1] Neoplasms of unknown behaviour of rectum Also known as: Neoplasms of unknown behaviour of rectum | rectum tumour NOS [8E21] Permanent vegetative state Definition: Prognostic term applied to patients in a persistent vegetative state for whom no recovery is expected. Also known as: Permanent vegetative state === GRAPH WALKS === --- Walk 1 --- [QF01.Y] Other specified acquired absence of organs --PARENT--> [QF01] Acquired absence of organs --CHILD--> [QF01.1] Acquired absence of genital organs --- Walk 2 --- [QF01.Y] Other specified acquired absence of organs --PARENT--> [QF01] Acquired absence of organs --CHILD--> [QF01.0] Acquired absence of breast --- Walk 3 --- [DC14.1] Postcholecystectomy syndrome Def: This describes the presence of abdominal symptoms after surgical removal of the gallbladder. Symptoms may include nausea and vomiting, bloating and diarrhoea, and pain in the upper right abdomen. The ... --PARENT--> [DC14] Certain specified biliary diseases Def: This is a group of conditions characterised as being in or associated with the biliary tract, the passageway for bile, which are not classified elsewhere.... --EXCLUDES--> [?] Benign neoplasm of gallbladder, extrahepatic bile ducts or ampulla of Vater --- Walk 4 --- [DC14.1] Postcholecystectomy syndrome Def: This describes the presence of abdominal symptoms after surgical removal of the gallbladder. Symptoms may include nausea and vomiting, bloating and diarrhoea, and pain in the upper right abdomen. The ... --PARENT--> [DC14] Certain specified biliary diseases Def: This is a group of conditions characterised as being in or associated with the biliary tract, the passageway for bile, which are not classified elsewhere.... --EXCLUDES--> [?] Malignant neoplasms of hepatobiliary system --- Walk 5 --- [GC01.0] Bladder neck obstruction Def: A condition of the bladder, caused by congenital or acquired abnormalities that impair the muscles that connect the bladder to the urethra. This condition is characterised by obstruction of the bladde... --PARENT--> [GC01] Other disorders of bladder Def: Any disorder characterised by pathological changes to the urinary bladder.... --CHILD--> [GC01.0] Bladder neck obstruction Def: A condition of the bladder, caused by congenital or acquired abnormalities that impair the muscles that connect the bladder to the urethra. This condition is characterised by obstruction of the bladde... --- Walk 6 --- [GC01.0] Bladder neck obstruction Def: A condition of the bladder, caused by congenital or acquired abnormalities that impair the muscles that connect the bladder to the urethra. This condition is characterised by obstruction of the bladde... --PARENT--> [GC01] Other disorders of bladder Def: Any disorder characterised by pathological changes to the urinary bladder.... --RELATED_TO--> [?] Bladder pain Def: Complaint of suprapubic or retropubic pain, pressure, or discomfort, related to the bladder, and usually increasing with bladder filling. It may persist or be relieved after voiding....
[ "[QF01.Y] Other specified acquired absence of organs\n --PARENT--> [QF01] Acquired absence of organs\n --CHILD--> [QF01.1] Acquired absence of genital organs", "[QF01.Y] Other specified acquired absence of organs\n --PARENT--> [QF01] Acquired absence of organs\n --CHILD--> [QF01.0] Acquired absence of breast", "[DC14.1] Postcholecystectomy syndrome\n Def: This describes the presence of abdominal symptoms after surgical removal of the gallbladder. Symptoms may include nausea and vomiting, bloating and diarrhoea, and pain in the upper right abdomen. The ...\n --PARENT--> [DC14] Certain specified biliary diseases\n Def: This is a group of conditions characterised as being in or associated with the biliary tract, the passageway for bile, which are not classified elsewhere....\n --EXCLUDES--> [?] Benign neoplasm of gallbladder, extrahepatic bile ducts or ampulla of Vater", "[DC14.1] Postcholecystectomy syndrome\n Def: This describes the presence of abdominal symptoms after surgical removal of the gallbladder. Symptoms may include nausea and vomiting, bloating and diarrhoea, and pain in the upper right abdomen. The ...\n --PARENT--> [DC14] Certain specified biliary diseases\n Def: This is a group of conditions characterised as being in or associated with the biliary tract, the passageway for bile, which are not classified elsewhere....\n --EXCLUDES--> [?] Malignant neoplasms of hepatobiliary system", "[GC01.0] Bladder neck obstruction\n Def: A condition of the bladder, caused by congenital or acquired abnormalities that impair the muscles that connect the bladder to the urethra. This condition is characterised by obstruction of the bladde...\n --PARENT--> [GC01] Other disorders of bladder\n Def: Any disorder characterised by pathological changes to the urinary bladder....\n --CHILD--> [GC01.0] Bladder neck obstruction\n Def: A condition of the bladder, caused by congenital or acquired abnormalities that impair the muscles that connect the bladder to the urethra. This condition is characterised by obstruction of the bladde...", "[GC01.0] Bladder neck obstruction\n Def: A condition of the bladder, caused by congenital or acquired abnormalities that impair the muscles that connect the bladder to the urethra. This condition is characterised by obstruction of the bladde...\n --PARENT--> [GC01] Other disorders of bladder\n Def: Any disorder characterised by pathological changes to the urinary bladder....\n --RELATED_TO--> [?] Bladder pain\n Def: Complaint of suprapubic or retropubic pain, pressure, or discomfort, related to the bladder, and usually increasing with bladder filling. It may persist or be relieved after voiding...." ]
QF01.Y
Other specified acquired absence of organs
[ { "from_icd11": "QF01.Y", "icd10_code": "Z9049", "icd10_title": "Acquired absence of other specified parts of digestive tract" }, { "from_icd11": "DC14.1", "icd10_code": "K915", "icd10_title": "Postcholecystectomy syndrome" }, { "from_icd11": "GC01.0", "icd10_code": "N320", "icd10_title": "Bladder-neck obstruction" }, { "from_icd11": "4A01.03", "icd10_code": "D807", "icd10_title": "Transient hypogammaglobulinemia of infancy" }, { "from_icd11": "DB30.4", "icd10_code": "K624", "icd10_title": "Stenosis of anus and rectum" }, { "from_icd11": "2F90.1", "icd10_code": "D375", "icd10_title": "Neoplasm of uncertain behavior of rectum" }, { "from_icd11": "8E21", "icd10_code": "R402142", "icd10_title": "Coma scale, eyes open, spontaneous, at arrival to emergency department" }, { "from_icd11": "8E21", "icd10_code": "R402362", "icd10_title": "Coma scale, best motor response, obeys commands, at arrival to emergency department" }, { "from_icd11": "8E21", "icd10_code": "R402252", "icd10_title": "Coma scale, best verbal response, oriented, at arrival to emergency department" }, { "from_icd11": "8E21", "icd10_code": "R402412", "icd10_title": "Glasgow coma scale score 13-15, at arrival to emergency department" }, { "from_icd11": "8E21", "icd10_code": "R4020", "icd10_title": "Unspecified coma" }, { "from_icd11": "8E21", "icd10_code": "R402141", "icd10_title": "Coma scale, eyes open, spontaneous, in the field [EMT or ambulance]" }, { "from_icd11": "8E21", "icd10_code": "R402361", "icd10_title": "Coma scale, best motor response, obeys commands, in the field [EMT or ambulance]" }, { "from_icd11": "8E21", "icd10_code": "R402251", "icd10_title": "Coma scale, best verbal response, oriented, in the field [EMT or ambulance]" }, { "from_icd11": "8E21", "icd10_code": "R402413", "icd10_title": "Glasgow coma scale score 13-15, at hospital admission" } ]
Z9049
Acquired absence of other specified parts of digestive tract
A 41-year-old white female with no relevant past medical history became pregnant at 35 years old, which was the only pregnancy to date. At 25 weeks of gestation, while straining by lifting weights, she suddenly developed acute pulmonary oedema with mild hypotension (81/42 mmHg). The ECG showed sinus tachycardia, associated to mild troponin I elevation (0.97 ng/mL; 0–0.06), high brain natriuretic peptide levels (750 pg/mL; 0–100) and a left ventricular ejection fraction (LVEF) of 38%, with global hypokinesia on transthoracic echocardiogram (TTE). No other symptoms or signs including fever, or drug abuse were reported. Preeclampsia was ruled out as the patient was mild hypotensive and did not have proteinuria or peripheral edema. No other laboratory abnormalities were found, particularly regarding the inflammatory makers and liver enzymes. Viral screening for enterovirus including echo and coxsackie, adenovirus, parvovirus, cytomegalovirus and Ebstein-Barr virus was negative, and autoimmune screening including antinuclear antibodies, anticardiolipin antibodies, anti-b2GP1, antineutrophil cytoplasmic antibodies, C3 and C4 was unremarkable. Computed tomography angiography excluded pulmonary embolism. The patient improved in 48 hours on intravenous furosemide with complete LVEF recovery. No further complications occurred, including at the delivery at 37 weeks, which excluded peripartum cardiomyopathy.
4.023438
0.979492
sec[1]/p[0]
en
0.999995
24987459
https://doi.org/10.1186/1755-7682-7-30
[ "including", "antibodies", "which", "pulmonary", "lvef", "screening", "excluded", "white", "relevant", "past" ]
[ { "code": "7A24", "title": "Hypersomnia due to a medication or substance" }, { "code": "9D90", "title": "Vision impairment including blindness" }, { "code": "NE61", "title": "Harmful effects of or exposure to noxious substances, chiefly nonmedicinal as to source, not elsewhere classified" }, { "code": "3A50.02", "title": "Haemoglobin H disease (– α/– – included)" }, { "code": "LA8B.Z", "title": "Congenital anomaly of great arteries including arterial duct, unspecified" }, { "code": "JA86.Y", "title": "Maternal care for other specified fetal problems" }, { "code": "MA14.14", "title": "Anti-nuclear antibody positive" }, { "code": "MA14.13", "title": "Anti-nuclear antibody negative" }, { "code": "JA86.0", "title": "Maternal care for red cell antibodies" }, { "code": "MA14.1C", "title": "Raised antibody titre" } ]
=== ICD-11 CODES FOUND === [7A24] Hypersomnia due to a medication or substance Definition: Hypersomnia due to a medication or substance is characterised by excessive nocturnal sleep, daytime sleepiness, or excessive napping that is attributable to the sedating effects of medications, alcohol, or other psychoactive substances, including withdrawal syndromes (e.g., from stimulants) and is sufficiently severe to constitute an independent focus of clinical attention. Note: A definitive diagnosis requires use of polysomnography and multiple sleep latency test (MSLT) to rule out other hype Also known as: Hypersomnia due to a medication or substance | Hypersomnia due to substances including medications | Hypersomnolence due to substances including medications Includes: Hypersomnia due to substances including medications [9D90] Vision impairment including blindness Definition: !markdown The table below gives a classification of severity of vision impairment based on visual acuity.  For epidemiological studies, it is recommended to collect the following information on visual acuity for each eye, for both eyes open and for distance and near.  a) Uncorrected visual acuity  b) Presenting visual acuity  c) Best corrected visual acuity  Blindness is also categorized according to the degree of constriction of the central visual field in the better eye to less than 10 Also known as: Vision impairment including blindness [NE61] Harmful effects of or exposure to noxious substances, chiefly nonmedicinal as to source, not elsewhere classified Also known as: Harmful effects of or exposure to noxious substances, chiefly nonmedicinal as to source, not elsewhere classified | Harmful effects of or exposure to noxious substances chiefly nonmedicinal as to source, alcohols | alcohol poisoning | alcohol toxicity | Harmful effects of or exposure to noxious substances chiefly nonmedicinal as to source, Ethanol Excludes: corrosions | Bacterial foodborne intoxications [3A50.02] Haemoglobin H disease (– α/– – included) Definition: Haemoglobin H (HbH) disease is a moderate to severe form of alpha-thalassemia characterised by pronounced microcytic hypochromic haemolytic anaemia. Also known as: Haemoglobin H disease (– α/– – included) | alpha - /- - or mutational forms of alpha-thalassaemia | Alpha thalassaemia intermedia [LA8B.Z] Congenital anomaly of great arteries including arterial duct, unspecified Also known as: Congenital anomaly of great arteries including arterial duct, unspecified | Congenital anomaly of great arteries including arterial duct [JA86.Y] Maternal care for other specified fetal problems Also known as: Maternal care for other specified fetal problems | Maternal care for other isoimmunization | Isoimmunization NOS | maternal antibodies NOS | pregnancy management affected by incompatibility of blood groups NOS [MA14.14] Anti-nuclear antibody positive Also known as: Anti-nuclear antibody positive | ANA - [anti-nuclear antibody] positive [MA14.13] Anti-nuclear antibody negative Also known as: Anti-nuclear antibody negative | ANA - [anti-nuclear antibody] negative [JA86.0] Maternal care for red cell antibodies Definition: Maternal care for rhesus or other isoimmunization Also known as: Maternal care for red cell antibodies | Maternal care for rhesus isoimmunization | Rh factor immunization affecting management of pregnancy | Rh incompatibility | Rh incompatibility with hydrops fetalis [MA14.1C] Raised antibody titre Also known as: Raised antibody titre | antibody titre above reference range | high antibody titre | increased antibody titre Excludes: isoimmunization, in pregnancy affecting fetus or newborn === GRAPH WALKS === --- Walk 1 --- [7A24] Hypersomnia due to a medication or substance Def: Hypersomnia due to a medication or substance is characterised by excessive nocturnal sleep, daytime sleepiness, or excessive napping that is attributable to the sedating effects of medications, alcoho... --PARENT--> [?] Hypersomnolence disorders Def: Hypersomnolence disorders are characterised by a complaint of daytime sleepiness that is not due to another sleep-wake disorder (e.g. disturbed nocturnal sleep, misaligned circadian rhythm, or breathi... --PARENT--> [07] Sleep-wake disorders Def: Sleep-wake disorders are characterised by difficulty initiating or maintaining sleep (insomnia disorders), excessive sleepiness (hypersomnolence disorders), respiratory disturbance during sleep (sleep... --- Walk 2 --- [7A24] Hypersomnia due to a medication or substance Def: Hypersomnia due to a medication or substance is characterised by excessive nocturnal sleep, daytime sleepiness, or excessive napping that is attributable to the sedating effects of medications, alcoho... --PARENT--> [?] Hypersomnolence disorders Def: Hypersomnolence disorders are characterised by a complaint of daytime sleepiness that is not due to another sleep-wake disorder (e.g. disturbed nocturnal sleep, misaligned circadian rhythm, or breathi... --CHILD--> [7A21] Idiopathic hypersomnia Def: Idiopathic hypersomnia is characterised by daily periods of irrepressible need to sleep or daytime lapses into sleep occurring for at least several months in the absence of cataplexy or hypocretin def... --- Walk 3 --- [9D90] Vision impairment including blindness Def: !markdown The table below gives a classification of severity of vision impairment based on visual acuity.  For epidemiological studies, it is recommended to collect the following information on visual... --RELATED_TO--> [?] No vision impairment --PARENT--> [?] Vision impairment including blindness Def: !markdown The table below gives a classification of severity of vision impairment based on visual acuity.  For epidemiological studies, it is recommended to collect the following information on visual... --- Walk 4 --- [9D90] Vision impairment including blindness Def: !markdown The table below gives a classification of severity of vision impairment based on visual acuity.  For epidemiological studies, it is recommended to collect the following information on visual... --PARENT--> [?] Vision impairment Def: A vision impairment results when an eye condition affects the visual system and one or more of its vision functions. Typically, population-based surveys measure visual impairment using exclusively vis... --CHILD--> [9D93] Complex vision-related dysfunctions Def: Complex Vision-Related Dysfunctions involve interactions with other sensory and motor systems. They reflect the combined effects at all stages of processing.... --- Walk 5 --- [NE61] Harmful effects of or exposure to noxious substances, chiefly nonmedicinal as to source, not elsewhere classified --EXCLUDES--> [?] Burns Def: A burn is an injury to the tissues caused by a pathological flux of energy which causes cellular destruction and irreversible denaturation of proteins and is primarily caused by thermal or other acute... --CHILD--> [?] Burns of external body surface, specified by site --- Walk 6 --- [NE61] Harmful effects of or exposure to noxious substances, chiefly nonmedicinal as to source, not elsewhere classified --EXCLUDES--> [?] Bacterial foodborne intoxications Def: Any condition caused by an intoxication due to a bacterial toxin. Intoxication is by ingestion of contaminated food.... --EXCLUDES--> [?] Harmful effects of or exposure to noxious substances, Substances chiefly nonmedicinal as to source, Other noxious substances eaten as food
[ "[7A24] Hypersomnia due to a medication or substance\n Def: Hypersomnia due to a medication or substance is characterised by excessive nocturnal sleep, daytime sleepiness, or excessive napping that is attributable to the sedating effects of medications, alcoho...\n --PARENT--> [?] Hypersomnolence disorders\n Def: Hypersomnolence disorders are characterised by a complaint of daytime sleepiness that is not due to another sleep-wake disorder (e.g. disturbed nocturnal sleep, misaligned circadian rhythm, or breathi...\n --PARENT--> [07] Sleep-wake disorders\n Def: Sleep-wake disorders are characterised by difficulty initiating or maintaining sleep (insomnia disorders), excessive sleepiness (hypersomnolence disorders), respiratory disturbance during sleep (sleep...", "[7A24] Hypersomnia due to a medication or substance\n Def: Hypersomnia due to a medication or substance is characterised by excessive nocturnal sleep, daytime sleepiness, or excessive napping that is attributable to the sedating effects of medications, alcoho...\n --PARENT--> [?] Hypersomnolence disorders\n Def: Hypersomnolence disorders are characterised by a complaint of daytime sleepiness that is not due to another sleep-wake disorder (e.g. disturbed nocturnal sleep, misaligned circadian rhythm, or breathi...\n --CHILD--> [7A21] Idiopathic hypersomnia\n Def: Idiopathic hypersomnia is characterised by daily periods of irrepressible need to sleep or daytime lapses into sleep occurring for at least several months in the absence of cataplexy or hypocretin def...", "[9D90] Vision impairment including blindness\n Def: !markdown\nThe table below gives a classification of severity of vision impairment based on visual acuity. \nFor epidemiological studies, it is recommended to collect the following information on visual...\n --RELATED_TO--> [?] No vision impairment\n --PARENT--> [?] Vision impairment including blindness\n Def: !markdown\nThe table below gives a classification of severity of vision impairment based on visual acuity. \nFor epidemiological studies, it is recommended to collect the following information on visual...", "[9D90] Vision impairment including blindness\n Def: !markdown\nThe table below gives a classification of severity of vision impairment based on visual acuity. \nFor epidemiological studies, it is recommended to collect the following information on visual...\n --PARENT--> [?] Vision impairment\n Def: A vision impairment results when an eye condition affects the visual system and one or more of its vision functions. Typically, population-based surveys measure visual impairment using exclusively vis...\n --CHILD--> [9D93] Complex vision-related dysfunctions\n Def: Complex Vision-Related Dysfunctions involve interactions with other sensory and motor systems. They reflect the combined effects at all stages of processing....", "[NE61] Harmful effects of or exposure to noxious substances, chiefly nonmedicinal as to source, not elsewhere classified\n --EXCLUDES--> [?] Burns\n Def: A burn is an injury to the tissues caused by a pathological flux of energy which causes cellular destruction and irreversible denaturation of proteins and is primarily caused by thermal or other acute...\n --CHILD--> [?] Burns of external body surface, specified by site", "[NE61] Harmful effects of or exposure to noxious substances, chiefly nonmedicinal as to source, not elsewhere classified\n --EXCLUDES--> [?] Bacterial foodborne intoxications\n Def: Any condition caused by an intoxication due to a bacterial toxin. Intoxication is by ingestion of contaminated food....\n --EXCLUDES--> [?] Harmful effects of or exposure to noxious substances, Substances chiefly nonmedicinal as to source, Other noxious substances eaten as food" ]
7A24
Hypersomnia due to a medication or substance
[ { "from_icd11": "7A24", "icd10_code": "G4719", "icd10_title": "Other hypersomnia" }, { "from_icd11": "7A24", "icd10_code": "G4710", "icd10_title": "Hypersomnia, unspecified" }, { "from_icd11": "7A24", "icd10_code": "G4712", "icd10_title": "Idiopathic hypersomnia without long sleep time" }, { "from_icd11": "7A24", "icd10_code": "G4714", "icd10_title": "Hypersomnia due to medical condition" }, { "from_icd11": "7A24", "icd10_code": "G4713", "icd10_title": "Recurrent hypersomnia" }, { "from_icd11": "7A24", "icd10_code": "G471", "icd10_title": "Hypersomnia" }, { "from_icd11": "9D90", "icd10_code": "H5461", "icd10_title": "Unqualified visual loss, right eye, normal vision left eye" }, { "from_icd11": "9D90", "icd10_code": "H5440", "icd10_title": "Blindness, one eye, unspecified eye" }, { "from_icd11": "9D90", "icd10_code": "H5442", "icd10_title": "Blindness, left eye, normal vision right eye" }, { "from_icd11": "9D90", "icd10_code": "H5441", "icd10_title": "Blindness, right eye, normal vision left eye" }, { "from_icd11": "9D90", "icd10_code": "H5462", "icd10_title": "Unqualified visual loss, left eye, normal vision right eye" }, { "from_icd11": "9D90", "icd10_code": "H5442A3", "icd10_title": "Blindness left eye category 3, normal vision right eye" }, { "from_icd11": "9D90", "icd10_code": "H54413A", "icd10_title": "Blindness right eye category 3, normal vision left eye" }, { "from_icd11": "9D90", "icd10_code": "H5442A5", "icd10_title": "Blindness left eye category 5, normal vision right eye" }, { "from_icd11": "9D90", "icd10_code": "H5460", "icd10_title": "Unqualified visual loss, one eye, unspecified" } ]
G4719
Other hypersomnia
A 58-year-old woman with a history of hypertension and cardiomyopathy fell onto her face while running to join her family in another room. The family heard her fall and found her with her neck hyperextended against a wall. The patient was not breathing, and the family immediately administered cardiopulmonary resuscitation. She was intubated and resuscitated from pulseless electrical arrest by the emergency medical services. Computed tomography imaging showed a type III odontoid fracture ( Figure 1(a) ) and a Jefferson-type fracture of the atlas (not shown). The patient had ST elevation on electrocardiogram and underwent emergent cardiac catheterization, which did not demonstrate an occluded vessel. It did show severe systolic heart failure with an ejection fraction of 15%, and the patient required multiple pressors to keep her heart beating. The patient awoke alert but quadriplegic. Magnetic resonance imaging of her cervical spine showed a cervical cord contusion behind C2 with abnormal signal from the medulla to the inferior C3 level ( Figure 1(b) ). She was fully dependent on a ventilator and required an external pacemaker because of repetitive bradyarrhythmias and asystolic pauses. Because of the low quality of life inherent in being a C2 quadriplegic with complete paralysis below the neck and lifelong ventilator dependence, the patient and family elected to withdraw care and the patient died.
3.792969
0.983398
sec[1]/p[0]
en
0.999998
24826344
https://doi.org/10.1155/2012/821565
[ "family", "neck", "imaging", "type", "fracture", "heart", "required", "quadriplegic", "cervical", "ventilator" ]
[ { "code": "QE70.Z", "title": "Problems related to primary support group, including family circumstances, unspecified" }, { "code": "8C74.1Z", "title": "Periodic paralysis, unspecified" }, { "code": "2B90.Y", "title": "Other specified malignant neoplasms of colon" }, { "code": "EE61", "title": "Superficial fibromatoses" }, { "code": "9B70", "title": "Inherited retinal dystrophies" }, { "code": "ME86.C", "title": "Symptom or complaint of the neck" }, { "code": "LA6Z", "title": "Structural developmental anomalies of the neck, unspecified" }, { "code": "ME84.0", "title": "Cervical spine pain" }, { "code": "FA71", "title": "Torticollis" }, { "code": "NA23.4Y", "title": "Other specified strain or sprain of cervical spine" } ]
=== ICD-11 CODES FOUND === [QE70.Z] Problems related to primary support group, including family circumstances, unspecified Also known as: Problems related to primary support group, including family circumstances, unspecified | Problems related to primary support group, including family circumstances | family problem | problem related to primary support group | Problem related to gambling in the family [8C74.1Z] Periodic paralysis, unspecified Also known as: Periodic paralysis, unspecified | Periodic paralysis | Westphal disease | periodic myotonia | myoplegic dystrophy [2B90.Y] Other specified malignant neoplasms of colon Also known as: Other specified malignant neoplasms of colon | Neuroendocrine neoplasm of colon | Colon endocrine neoplasm | Neuroendocrine carcinoma of colon | NEC - [neuroendocrine carcinoma] of colon [EE61] Superficial fibromatoses Also known as: Superficial fibromatoses | Pachydermodactyly | Camptodactyly or streblodactyly | Familial camptodactyly | Sporadic camptodactyly [9B70] Inherited retinal dystrophies Also known as: Inherited retinal dystrophies | hereditary retinal dystrophies | Amaurosis - hypertrichosis | Autosomal dominant late-onset retinal degeneration | Bothnia retinal dystrophy Includes: Leber congenital amaurosis | Stargardt disease | Vitreoretinal dystrophy [ME86.C] Symptom or complaint of the neck Also known as: Symptom or complaint of the neck | Neck syndrome Excludes: Chronic primary musculoskeletal pain | Chronic secondary musculoskeletal pain [LA6Z] Structural developmental anomalies of the neck, unspecified Also known as: Structural developmental anomalies of the neck, unspecified | Malformations of the neck [ME84.0] Cervical spine pain Definition: This is a condition which is usually characterised by pain or discomfort in the neck region and can be caused by numerous spinal problems. It may be a feature of virtually every disorder and disease that occurs above the shoulder blades. Also known as: Cervical spine pain | cervical pain | neck ache | nonspecific pain in the neck region | cervicalgia Includes: cervicalgia Excludes: cervical disc degeneration | Chronic primary cervical pain | Chronic secondary musculoskeletal pain [FA71] Torticollis Also known as: Torticollis | contracture of neck | wry neck | wry neck/torticollis | Intermittent torticollis Excludes: Cervical dystonia | Congenital torticollis | current injury - see injury of spine by body region [NA23.4Y] Other specified strain or sprain of cervical spine Also known as: Other specified strain or sprain of cervical spine | Strain of cervical spine | cervical strain | Strain of cervical anterior longitudinal ligament | Sprain of cervical spine === GRAPH WALKS === --- Walk 1 --- [QE70.Z] Problems related to primary support group, including family circumstances, unspecified --PARENT--> [QE70] Problems related to primary support group, including family circumstances --EXCLUDES--> [?] Problems associated with upbringing --- Walk 2 --- [QE70.Z] Problems related to primary support group, including family circumstances, unspecified --PARENT--> [QE70] Problems related to primary support group, including family circumstances --CHILD--> [QE70.2] Dependent relative needing care at home --- Walk 3 --- [8C74.1Z] Periodic paralysis, unspecified --PARENT--> [8C74.1] Periodic paralysis Def: Rare group of neuromuscular disorders that are associated with defects in ion channels. Characterized by intermittent episodes of severe weakness of the limbs usually after heavy exercise, fasting, or... --CHILD--> [8C74.1Y] Other specified periodic paralysis --- Walk 4 --- [8C74.1Z] Periodic paralysis, unspecified --PARENT--> [8C74.1] Periodic paralysis Def: Rare group of neuromuscular disorders that are associated with defects in ion channels. Characterized by intermittent episodes of severe weakness of the limbs usually after heavy exercise, fasting, or... --CHILD--> [8C74.10] Hypokalaemic periodic paralysis Def: Hypokalaemic periodic paralysis (hypoPP) is a muscle channelopathy characterised by episodes of muscle paralysis lasting from a few to 24-48 hours and associated with a fall in blood potassium levels.... --- Walk 5 --- [2B90.Y] Other specified malignant neoplasms of colon --PARENT--> [2B90] Malignant neoplasms of colon Def: Primary malignant neoplasms arising in the colon.... --RELATED_TO--> [?] Gardner syndrome Def: Gardner syndrome develops adenomatous polyps throughout the gastrointestinal tract, accompanied by extracolonic manifestations, including periampullary adenomas, papillary carcinoma of the thyroid, he... --- Walk 6 --- [2B90.Y] Other specified malignant neoplasms of colon --PARENT--> [2B90] Malignant neoplasms of colon Def: Primary malignant neoplasms arising in the colon.... --RELATED_TO--> [?] Malignant Lymphoma of colon Def: A solid tumour of large intestine that begins in lymphocytes, a type of cells that forms part of the immune system, begin behaving abnormally and invasive, of the large intestine....
[ "[QE70.Z] Problems related to primary support group, including family circumstances, unspecified\n --PARENT--> [QE70] Problems related to primary support group, including family circumstances\n --EXCLUDES--> [?] Problems associated with upbringing", "[QE70.Z] Problems related to primary support group, including family circumstances, unspecified\n --PARENT--> [QE70] Problems related to primary support group, including family circumstances\n --CHILD--> [QE70.2] Dependent relative needing care at home", "[8C74.1Z] Periodic paralysis, unspecified\n --PARENT--> [8C74.1] Periodic paralysis\n Def: Rare group of neuromuscular disorders that are associated with defects in ion channels. Characterized by intermittent episodes of severe weakness of the limbs usually after heavy exercise, fasting, or...\n --CHILD--> [8C74.1Y] Other specified periodic paralysis", "[8C74.1Z] Periodic paralysis, unspecified\n --PARENT--> [8C74.1] Periodic paralysis\n Def: Rare group of neuromuscular disorders that are associated with defects in ion channels. Characterized by intermittent episodes of severe weakness of the limbs usually after heavy exercise, fasting, or...\n --CHILD--> [8C74.10] Hypokalaemic periodic paralysis\n Def: Hypokalaemic periodic paralysis (hypoPP) is a muscle channelopathy characterised by episodes of muscle paralysis lasting from a few to 24-48 hours and associated with a fall in blood potassium levels....", "[2B90.Y] Other specified malignant neoplasms of colon\n --PARENT--> [2B90] Malignant neoplasms of colon\n Def: Primary malignant neoplasms arising in the colon....\n --RELATED_TO--> [?] Gardner syndrome\n Def: Gardner syndrome develops adenomatous polyps throughout the gastrointestinal tract, accompanied by extracolonic manifestations, including periampullary adenomas, papillary carcinoma of the thyroid, he...", "[2B90.Y] Other specified malignant neoplasms of colon\n --PARENT--> [2B90] Malignant neoplasms of colon\n Def: Primary malignant neoplasms arising in the colon....\n --RELATED_TO--> [?] Malignant Lymphoma of colon\n Def: A solid tumour of large intestine that begins in lymphocytes, a type of cells that forms part of the immune system, begin behaving abnormally and invasive, of the large intestine...." ]
QE70.Z
Problems related to primary support group, including family circumstances, unspecified
[ { "from_icd11": "QE70.Z", "icd10_code": "Z6379", "icd10_title": "Other stressful life events affecting family and household" }, { "from_icd11": "QE70.Z", "icd10_code": "Z6372", "icd10_title": "Alcoholism and drug addiction in family" }, { "from_icd11": "QE70.Z", "icd10_code": "Z638", "icd10_title": "Other specified problems related to primary support group" }, { "from_icd11": "QE70.Z", "icd10_code": "Z639", "icd10_title": "Problem related to primary support group, unspecified" }, { "from_icd11": "QE70.Z", "icd10_code": "Z637", "icd10_title": "Other stressful life events affecting family and household" }, { "from_icd11": "8C74.1Z", "icd10_code": "G723", "icd10_title": "Periodic paralysis" }, { "from_icd11": "EE61", "icd10_code": "F54", "icd10_title": "Psychological and behavioral factors associated with disorders or diseases classified elsewhere" }, { "from_icd11": "9B70", "icd10_code": "H3552", "icd10_title": "Pigmentary retinal dystrophy" }, { "from_icd11": "9B70", "icd10_code": "H3550", "icd10_title": "Unspecified hereditary retinal dystrophy" }, { "from_icd11": "9B70", "icd10_code": "H3553", "icd10_title": "Other dystrophies primarily involving the sensory retina" }, { "from_icd11": "9B70", "icd10_code": "H3554", "icd10_title": "Dystrophies primarily involving the retinal pigment epithelium" }, { "from_icd11": "9B70", "icd10_code": "H355", "icd10_title": "Hereditary retinal dystrophy" }, { "from_icd11": "LA6Z", "icd10_code": "Q680", "icd10_title": "Congenital deformity of sternocleidomastoid muscle" }, { "from_icd11": "LA6Z", "icd10_code": "Q180", "icd10_title": "Sinus, fistula and cyst of branchial cleft" }, { "from_icd11": "LA6Z", "icd10_code": "Q188", "icd10_title": "Other specified congenital malformations of face and neck" } ]
Z6379
Other stressful life events affecting family and household
A 48 years old-black Senegalese woman was hospitalized in June 2011 for cholestatic jaundice, right upper quadrant pain, fever and weak general condition with weight loss of 15 kg in 2 months. She had no medical or surgical history or pre-existing medical condition. On physical examination, she had jaundice and fever (38.5 °C). The abdomen was soft, painful to palpation of the right upper quadrant with hepatomegaly. She had no peripheral lymph nodes or splenomegaly. Laboratory investigations showed a discrete cytolysis with aspartate aminotransferase (AST) = 62 IU/l (2 N), alanine aminotransferase (ALT) = 49 IU/l (1,3 N), cholestasis with alkaline phosphatase (ALP) to 367 IU/l (2.7 N), GGT 291 IU/l (3.4 N), total bilirubin : 118.3 mg/l, with conjugated fraction to 77.3 mg/l, without liver deficiency [prothrombin time (PT) = 81 % albumin = 36 g/l]. There was an inflammation, with an erythrocyte sedimentation rate of 33 mm in the first hour, a serum fibrin to 4.1 g/l, and polyclonal hypergammaglobulinemia (31 g/l). The blood cell count and renal functions were normal. The alpha-fetoprotein levels were normal (3.7 ng/ml). Search of acid-fast bacilli by gastric aspirate was negative. The viral serology [hepatitis B virus (HBV), hepatitis C virus (HCV), human immunodeficiency virus (HIV), human T-lymphotropic virus 1 (HTLV1)] were negative. The urine cultures were sterile, without hematuria or pyuria.
3.904297
0.981445
sec[1]/p[0]
en
0.999997
27324380
https://doi.org/10.1186/s13104-016-2091-6
[ "virus", "jaundice", "quadrant", "fever", "aminotransferase", "without", "hepatitis", "human", "black", "senegalese" ]
[ { "code": "1D9Z", "title": "Unspecified viral infection of unspecified site" }, { "code": "1E1Z", "title": "Unspecified viral disease" }, { "code": "1E1Y", "title": "Other specified viral diseases" }, { "code": "1D85.Z", "title": "Viral carditis, unspecified" }, { "code": "KA62.Z", "title": "Viral infection in the fetus or newborn, unspecified" }, { "code": "ME10.1", "title": "Unspecified jaundice" }, { "code": "DC10.02", "title": "Obstruction of bile duct" }, { "code": "3A2Z", "title": "Acquired haemolytic anaemia, unspecified" }, { "code": "KA87.Y", "title": "Other specified neonatal hyperbilirubinaemia" }, { "code": "KA86", "title": "Neonatal kernicterus" } ]
=== ICD-11 CODES FOUND === [1D9Z] Unspecified viral infection of unspecified site Also known as: Unspecified viral infection of unspecified site | viral infection NOS | viral disorder NOS | disease caused by virus | unspecified viremia [1E1Z] Unspecified viral disease Also known as: Unspecified viral disease [1E1Y] Other specified viral diseases Also known as: Other specified viral diseases | Acute infectious lymphocytosis [1D85.Z] Viral carditis, unspecified Also known as: Viral carditis, unspecified | Viral carditis [KA62.Z] Viral infection in the fetus or newborn, unspecified Also known as: Viral infection in the fetus or newborn, unspecified | Viral infection in the fetus or newborn | congenital virus disorder | congenital virus disease [ME10.1] Unspecified jaundice Definition: A clinical manifestation of hyperbilirubinemia of unspecified origin, characterised by the yellowish staining of the skin; mucus membranes and sclera. Also known as: Unspecified jaundice | icteric | icterus | jaundice | jaundiced Excludes: neonatal jaundice [DC10.02] Obstruction of bile duct Also known as: Obstruction of bile duct | extrahepatic biliary obstruction | extrahepatic bile duct obstruction | bile duct obstruction | bile stasis Excludes: with cholelithiasis [3A2Z] Acquired haemolytic anaemia, unspecified Also known as: Acquired haemolytic anaemia, unspecified | Acquired haematogenous icterus | haematogenous icterus | haematogenous jaundice | Acquired haemolytic icterus [KA87.Y] Other specified neonatal hyperbilirubinaemia Also known as: Other specified neonatal hyperbilirubinaemia | Neonatal hyperbilirubinaemia due to skin bruising | Neonatal hyperbilirubinemia secondary to skin bruising | Neonatal hyperbilirubinaemia due to internal bleeding | Neonatal hyperbilirubinemia secondary to internal bleeding [KA86] Neonatal kernicterus Definition: Kernicterus is a pathologic diagnosis of the neonate that is characterised by yellow staining of the basal ganglia following elevated bilirubin concentrations in the blood and/or a breech in the blood brain barrier more common in the premature infant or the sick term neonate. It is characterised later in infancy and childhood by hearing deficits, choreoathetosis, and varying degrees of cognitive deficit. Also known as: Neonatal kernicterus | bilirubin encephalopathy | nuclear jaundice | kernicterus of newborn NOS | hyperbilirubinaemia encephalopathy Excludes: kernicterus due to inborn errors of metabolism === GRAPH WALKS === --- Walk 1 --- [1D9Z] Unspecified viral infection of unspecified site --PARENT--> [?] Viral infection of unspecified site --EXCLUDES--> [?] Herpes simplex infections Def: Any condition caused by an infection with herpes simplex virus (human herpesviruses 1 and 2). Confirmation is by identification of herpes simplex virus type 1 or 2.... --- Walk 2 --- [1D9Z] Unspecified viral infection of unspecified site --PARENT--> [?] Viral infection of unspecified site --PARENT--> [?] Certain other viral diseases --- Walk 3 --- [1E1Z] Unspecified viral disease --PARENT--> [?] Certain other viral diseases --CHILD--> [1D81] Infectious mononucleosis Def: A disease typically caused by an infection with Epstein-Barr virus or cytomegalovirus. This disease commonly presents with extreme fatigue, fever, acute pharyngitis, body aches, or lymphadenopathy. Tr... --- Walk 4 --- [1E1Z] Unspecified viral disease --PARENT--> [?] Certain other viral diseases --CHILD--> [1D81] Infectious mononucleosis Def: A disease typically caused by an infection with Epstein-Barr virus or cytomegalovirus. This disease commonly presents with extreme fatigue, fever, acute pharyngitis, body aches, or lymphadenopathy. Tr... --- Walk 5 --- [1E1Y] Other specified viral diseases --PARENT--> [?] Certain other viral diseases --CHILD--> [1D81] Infectious mononucleosis Def: A disease typically caused by an infection with Epstein-Barr virus or cytomegalovirus. This disease commonly presents with extreme fatigue, fever, acute pharyngitis, body aches, or lymphadenopathy. Tr... --- Walk 6 --- [1E1Y] Other specified viral diseases --PARENT--> [?] Certain other viral diseases --RELATED_TO--> [?] Viral duodenitis Def: Duodenitis caused by infection with virus. This includes infection with cytomegalovirus, herpes virus, HIV and other viral infections in the duodenum....
[ "[1D9Z] Unspecified viral infection of unspecified site\n --PARENT--> [?] Viral infection of unspecified site\n --EXCLUDES--> [?] Herpes simplex infections\n Def: Any condition caused by an infection with herpes simplex virus (human herpesviruses 1 and 2). Confirmation is by identification of herpes simplex virus type 1 or 2....", "[1D9Z] Unspecified viral infection of unspecified site\n --PARENT--> [?] Viral infection of unspecified site\n --PARENT--> [?] Certain other viral diseases", "[1E1Z] Unspecified viral disease\n --PARENT--> [?] Certain other viral diseases\n --CHILD--> [1D81] Infectious mononucleosis\n Def: A disease typically caused by an infection with Epstein-Barr virus or cytomegalovirus. This disease commonly presents with extreme fatigue, fever, acute pharyngitis, body aches, or lymphadenopathy. Tr...", "[1E1Z] Unspecified viral disease\n --PARENT--> [?] Certain other viral diseases\n --CHILD--> [1D81] Infectious mononucleosis\n Def: A disease typically caused by an infection with Epstein-Barr virus or cytomegalovirus. This disease commonly presents with extreme fatigue, fever, acute pharyngitis, body aches, or lymphadenopathy. Tr...", "[1E1Y] Other specified viral diseases\n --PARENT--> [?] Certain other viral diseases\n --CHILD--> [1D81] Infectious mononucleosis\n Def: A disease typically caused by an infection with Epstein-Barr virus or cytomegalovirus. This disease commonly presents with extreme fatigue, fever, acute pharyngitis, body aches, or lymphadenopathy. Tr...", "[1E1Y] Other specified viral diseases\n --PARENT--> [?] Certain other viral diseases\n --RELATED_TO--> [?] Viral duodenitis\n Def: Duodenitis caused by infection with virus. This includes infection with cytomegalovirus, herpes virus, HIV and other viral infections in the duodenum...." ]
1D9Z
Unspecified viral infection of unspecified site
[ { "from_icd11": "1D9Z", "icd10_code": "B348", "icd10_title": "Other viral infections of unspecified site" }, { "from_icd11": "1D9Z", "icd10_code": "B349", "icd10_title": "Viral infection, unspecified" }, { "from_icd11": "1D9Z", "icd10_code": "B344", "icd10_title": "Papovavirus infection, unspecified" }, { "from_icd11": "1D9Z", "icd10_code": "B333", "icd10_title": "Retrovirus infections, not elsewhere classified" }, { "from_icd11": "1D9Z", "icd10_code": "B34", "icd10_title": "Viral infection of unspecified site" }, { "from_icd11": "1E1Z", "icd10_code": "B338", "icd10_title": "Other specified viral diseases" }, { "from_icd11": "1E1Z", "icd10_code": "B25-B34", "icd10_title": "" }, { "from_icd11": "1E1Z", "icd10_code": "B33", "icd10_title": "Other viral diseases, not elsewhere classified" }, { "from_icd11": "1E1Z", "icd10_code": "M015", "icd10_title": "" }, { "from_icd11": "1E1Y", "icd10_code": "B9789", "icd10_title": "Other viral agents as the cause of diseases classified elsewhere" }, { "from_icd11": "1D85.Z", "icd10_code": "B3324", "icd10_title": "Viral cardiomyopathy" }, { "from_icd11": "1D85.Z", "icd10_code": "B3323", "icd10_title": "Viral pericarditis" }, { "from_icd11": "1D85.Z", "icd10_code": "B332", "icd10_title": "Viral carditis" }, { "from_icd11": "KA62.Z", "icd10_code": "P35", "icd10_title": "Congenital viral diseases" }, { "from_icd11": "KA62.Z", "icd10_code": "P358", "icd10_title": "Other congenital viral diseases" } ]
B348
Other viral infections of unspecified site
A 41-year-old female presented ambulatory to the Emergency Department at 11:41 PM with a 3-week history of feeling generally unwell. She complained of severe myalgias, chills, and a fever two days earlier. She had been unable to go to work for the previous 4 days due to her illness. She admitted to taking ibuprofen, up to 800 mg every 2 hours for several days for her myalgias, but she and her husband denied any significant acetaminophen ingestion. She was hemodynamically unstable on presentation with a heart rate of 114 beats per minute and a blood pressure of 71/40 mm Hg. She was afebrile with a temperature of 36.4°C. Her respiratory rate was 18 breaths per minute, and her oxygen saturations were 98% on room air. She was alert and oriented with a GCS of 15 and was able to give a history of her illness. Her head and neck exam was unremarkable, and no oral lesions were documented. Her respiratory and cardiac examinations were normal. Her abdomen was soft and nontender with no organomegaly, and her skin was clear. A pelvic exam was not performed. Her past medical history was significant only for two uncomplicated pregnancies, a tubal ligation, and dysfunctional uterine bleeding. Her only medication was an oral contraceptive pill. Her social history was significant for 26 ounces of alcohol per week, mostly on weekends. There was no history of smoking, drug use, travel, or high-risk sexual behaviors.
3.535156
0.986816
sec[1]/p[0]
en
0.999997
24826316
https://doi.org/10.1155/2011/138341
[ "myalgias", "illness", "minute", "respiratory", "exam", "oral", "ambulatory", "emergency", "department", "feeling" ]
[ { "code": "FB56.2", "title": "Myalgia" }, { "code": "1D83", "title": "Epidemic myalgia" }, { "code": "DD92.1", "title": "Functional anorectal pain" }, { "code": "FB56.6", "title": "Other specified soft tissue disorders" }, { "code": "FA22", "title": "Polymyalgia rheumatica" }, { "code": "MG48", "title": "Unknown or unspecified causes of morbidity" }, { "code": "1D9Z", "title": "Unspecified viral infection of unspecified site" }, { "code": "6E8Z", "title": "Mental, behavioural or neurodevelopmental disorders, unspecified" }, { "code": "MG25", "title": "Feeling ill" }, { "code": "LA85.1", "title": "Transposition of the great arteries" } ]
=== ICD-11 CODES FOUND === [FB56.2] Myalgia Definition: This is a disorder characterised by pain in a muscle or group of muscles. Also known as: Myalgia | muscle ache | muscle soreness | muscular pain | myalgic Excludes: Chronic primary musculoskeletal pain | Chronic secondary musculoskeletal pain [1D83] Epidemic myalgia Definition: A disease caused by an infection with the group B Coxsackie virus. This disease is characterised by pleuritic pain, fever, or muscle swelling. Transmission is by the faecal-oral route. Also known as: Epidemic myalgia | Bornholm disease | Dabney's grip | Devil's grip | epidemic benign dry pleurisy Includes: Bornholm disease [DD92.1] Functional anorectal pain Definition: This group incorporates functional disorders which principally complaints pain in the anorectal regions. In this category two disorders (chronic proctalgia – Levator ani syndrome and proctalgia fugax) are distinguished on the basis of duration, frequency, and characteristic quality of pain. Also known as: Functional anorectal pain | Chronic proctalgia | Levator ani syndrome | levator syndrome | Levator spasm [FB56.6] Other specified soft tissue disorders Also known as: Other specified soft tissue disorders | Fat necrosis | fatty necrosis | Profichet's disease | Sloughing of fascia [FA22] Polymyalgia rheumatica Definition: Polymyalgia rheumatica (PMR) is a syndrome characterised by aching of the proximal portions of the extremities and torso. Provisional classification criteria for PMR by the European League Against Rheumatism/American College of Rheumatology Collaborative Initiative should be applied to patients aged 50 years or older with bilateral shoulder aching, and abnormal CRP and/or ESR. The scoring algorithm is based on morning stiffness >45 minutes (2 points), hip pain/limited range of motion (1 point), Also known as: Polymyalgia rheumatica | senile arthritis | polymyalgia arteritica | PMR - [polymyalgia rheumatica] | Forestier-Certonciny syndrome Excludes: Giant cell arteritis with polymyalgia rheumatica [MG48] Unknown or unspecified causes of morbidity Also known as: Unknown or unspecified causes of morbidity | undetermined cause | unknown cause of disease | illness | Illness NOS Includes: Undiagnosed disease, not specified as to the site or system involved [1D9Z] Unspecified viral infection of unspecified site Also known as: Unspecified viral infection of unspecified site | viral infection NOS | viral disorder NOS | disease caused by virus | unspecified viremia [6E8Z] Mental, behavioural or neurodevelopmental disorders, unspecified Also known as: Mental, behavioural or neurodevelopmental disorders, unspecified | Psychiatric disorder | mental disease NOS | mental disorder NOS | mental illness [MG25] Feeling ill Also known as: Feeling ill | malaise Includes: malaise [LA85.1] Transposition of the great arteries Definition: A congenital cardiovascular malformation in which the morphologically right ventricle or its remnant connects to the aorta and the morphologically left ventricle or its remnant connects to the pulmonary trunk. Also known as: Transposition of the great arteries | Discordant ventriculoarterial connection | complete transposition of great vessels | great vessels complete transposition | great vessels transposition === GRAPH WALKS === --- Walk 1 --- [FB56.2] Myalgia Def: This is a disorder characterised by pain in a muscle or group of muscles.... --PARENT--> [FB56] Specified soft tissue disorders, not elsewhere classified Def: This is a group of other disorders, which are not classified elsewhere, affecting tissues that connect, support, or surround other structures and organs of the body, not being bone.... --EXCLUDES--> [?] Mononeuropathy --- Walk 2 --- [FB56.2] Myalgia Def: This is a disorder characterised by pain in a muscle or group of muscles.... --EXCLUDES--> [?] Chronic secondary musculoskeletal pain Def: Chronic secondary musculoskeletal pain is chronic pain arising from bone(s), joint(s), muscle(s), vertebral column, tendon(s) or related soft tissue(s). It is a heterogeneous group of chronic pain con... --CHILD--> [?] Chronic secondary musculoskeletal pain from persistent inflammation Def: Chronic secondary musculoskeletal pain from persistent inflammation is chronic pain due to inflammatory mechanisms in joint(s), bone(s), tendon(s), muscle(s), soft tissue(s) or vertebral column. The p... --- Walk 3 --- [1D83] Epidemic myalgia Def: A disease caused by an infection with the group B Coxsackie virus. This disease is characterised by pleuritic pain, fever, or muscle swelling. Transmission is by the faecal-oral route.... --PARENT--> [?] Certain other viral diseases --RELATED_TO--> [?] Other viral diseases complicating pregnancy, childbirth or the puerperium --- Walk 4 --- [1D83] Epidemic myalgia Def: A disease caused by an infection with the group B Coxsackie virus. This disease is characterised by pleuritic pain, fever, or muscle swelling. Transmission is by the faecal-oral route.... --PARENT--> [?] Certain other viral diseases --RELATED_TO--> [?] Viral duodenitis Def: Duodenitis caused by infection with virus. This includes infection with cytomegalovirus, herpes virus, HIV and other viral infections in the duodenum.... --- Walk 5 --- [DD92.1] Functional anorectal pain Def: This group incorporates functional disorders which principally complaints pain in the anorectal regions. In this category two disorders (chronic proctalgia – Levator ani syndrome and proctalgia fugax)... --PARENT--> [DD92] Functional anorectal disorders Def: This group incorporates anorectal disorders which principally present anorectal and defecation complaints without apparent morphological changes of anorectal regions. However, the distinction between ... --CHILD--> [DD92.2] Functional defaecation disorders Def: Functional defaecation disorders are characterised by paradoxical contraction or inadequate relaxation of the pelvic floor muscles during attempted defaecation (dyssynergic defaecation) or inadequate ... --- Walk 6 --- [DD92.1] Functional anorectal pain Def: This group incorporates functional disorders which principally complaints pain in the anorectal regions. In this category two disorders (chronic proctalgia – Levator ani syndrome and proctalgia fugax)... --PARENT--> [DD92] Functional anorectal disorders Def: This group incorporates anorectal disorders which principally present anorectal and defecation complaints without apparent morphological changes of anorectal regions. However, the distinction between ... --EXCLUDES--> [?] Bodily distress disorder Def: Bodily distress disorder is characterised by the presence of bodily symptoms that are distressing to the individual and excessive attention directed toward the symptoms, which may be manifest by repea...
[ "[FB56.2] Myalgia\n Def: This is a disorder characterised by pain in a muscle or group of muscles....\n --PARENT--> [FB56] Specified soft tissue disorders, not elsewhere classified\n Def: This is a group of other disorders, which are not classified elsewhere, affecting tissues that connect, support, or surround other structures and organs of the body, not being bone....\n --EXCLUDES--> [?] Mononeuropathy", "[FB56.2] Myalgia\n Def: This is a disorder characterised by pain in a muscle or group of muscles....\n --EXCLUDES--> [?] Chronic secondary musculoskeletal pain\n Def: Chronic secondary musculoskeletal pain is chronic pain arising from bone(s), joint(s), muscle(s), vertebral column, tendon(s) or related soft tissue(s). It is a heterogeneous group of chronic pain con...\n --CHILD--> [?] Chronic secondary musculoskeletal pain from persistent inflammation\n Def: Chronic secondary musculoskeletal pain from persistent inflammation is chronic pain due to inflammatory mechanisms in joint(s), bone(s), tendon(s), muscle(s), soft tissue(s) or vertebral column. The p...", "[1D83] Epidemic myalgia\n Def: A disease caused by an infection with the group B Coxsackie virus. This disease is characterised by pleuritic pain, fever, or muscle swelling. Transmission is by the faecal-oral route....\n --PARENT--> [?] Certain other viral diseases\n --RELATED_TO--> [?] Other viral diseases complicating pregnancy, childbirth or the puerperium", "[1D83] Epidemic myalgia\n Def: A disease caused by an infection with the group B Coxsackie virus. This disease is characterised by pleuritic pain, fever, or muscle swelling. Transmission is by the faecal-oral route....\n --PARENT--> [?] Certain other viral diseases\n --RELATED_TO--> [?] Viral duodenitis\n Def: Duodenitis caused by infection with virus. This includes infection with cytomegalovirus, herpes virus, HIV and other viral infections in the duodenum....", "[DD92.1] Functional anorectal pain\n Def: This group incorporates functional disorders which principally complaints pain in the anorectal regions. In this category two disorders (chronic proctalgia – Levator ani syndrome and proctalgia fugax)...\n --PARENT--> [DD92] Functional anorectal disorders\n Def: This group incorporates anorectal disorders which principally present anorectal and defecation complaints without apparent morphological changes of anorectal regions. However, the distinction between ...\n --CHILD--> [DD92.2] Functional defaecation disorders\n Def: Functional defaecation disorders are characterised by paradoxical contraction or inadequate relaxation of the pelvic floor muscles during attempted defaecation (dyssynergic defaecation) or inadequate ...", "[DD92.1] Functional anorectal pain\n Def: This group incorporates functional disorders which principally complaints pain in the anorectal regions. In this category two disorders (chronic proctalgia – Levator ani syndrome and proctalgia fugax)...\n --PARENT--> [DD92] Functional anorectal disorders\n Def: This group incorporates anorectal disorders which principally present anorectal and defecation complaints without apparent morphological changes of anorectal regions. However, the distinction between ...\n --EXCLUDES--> [?] Bodily distress disorder\n Def: Bodily distress disorder is characterised by the presence of bodily symptoms that are distressing to the individual and excessive attention directed toward the symptoms, which may be manifest by repea..." ]
FB56.2
Myalgia
[ { "from_icd11": "FB56.2", "icd10_code": "M7918", "icd10_title": "Myalgia, other site" }, { "from_icd11": "FB56.2", "icd10_code": "M7910", "icd10_title": "Myalgia, unspecified site" }, { "from_icd11": "FB56.2", "icd10_code": "M7912", "icd10_title": "Myalgia of auxiliary muscles, head and neck" }, { "from_icd11": "FB56.2", "icd10_code": "M791", "icd10_title": "Myalgia" }, { "from_icd11": "1D83", "icd10_code": "B330", "icd10_title": "Epidemic myalgia" }, { "from_icd11": "DD92.1", "icd10_code": "K594", "icd10_title": "Anal spasm" }, { "from_icd11": "FB56.6", "icd10_code": "M7981", "icd10_title": "Nontraumatic hematoma of soft tissue" }, { "from_icd11": "FB56.6", "icd10_code": "M7989", "icd10_title": "Other specified soft tissue disorders" }, { "from_icd11": "FB56.6", "icd10_code": "M798", "icd10_title": "Other specified soft tissue disorders" }, { "from_icd11": "FA22", "icd10_code": "M353", "icd10_title": "Polymyalgia rheumatica" }, { "from_icd11": "FA22", "icd10_code": "M35", "icd10_title": "Other systemic involvement of connective tissue" }, { "from_icd11": "MG48", "icd10_code": "R69", "icd10_title": "Illness, unspecified" }, { "from_icd11": "1D9Z", "icd10_code": "B348", "icd10_title": "Other viral infections of unspecified site" }, { "from_icd11": "1D9Z", "icd10_code": "B349", "icd10_title": "Viral infection, unspecified" }, { "from_icd11": "1D9Z", "icd10_code": "B344", "icd10_title": "Papovavirus infection, unspecified" } ]
M7918
Myalgia, other site
The patient showed clinical improvement in aphasia and hemiparesis immediately after extubation. NCCT 24 hours after endovascular stroke therapy did not display signs of infarction or intracranial hemorrhage. On day 2 after endovascular stroke treatment, the patient was transferred to the hematology ward (NIHSS 5, mRS 3). A follow-up MRI was performed on day 10 after endovascular stroke treatment to evaluate the extent of a possible infarction and intracranial hemorrhage as possible contraindications to the continuation of chemotherapy. No hyperintensities on diffusion-weighted imaging (DWI), or changes of fluid attenuated inversion recovery (FLAIR) images as evidence of acute or subacute ischemia were detected . Time-of-flight MR angiography did not show a renewed occlusion. Fig. 1 Diffusion-weighted imaging (DWI, top row), apparent diffusion coefficient ( A , D , C , middle row) and fluid attenuated inversion recovery (FLAIR, bottom row) imaging at day 10 ( A , D and G ), day 23 ( B , E and H ), and day 92 ( C , F and I ) after endovascular recanalization of a left internal carotid artery occlusion. Please note the homogeneous white matter hyperintensity in the left anterior and middle cerebral artery territory on FLAIR images, which is not visible on day 10 ( G ), but on day 23 ( H ) and also on day 92 ( I ), sparing the subcortical U-fibers and with inconspicuous DWI at each corresponding MRI
4.03125
0.959961
sec[1]/p[3]
en
0.999995
36567313
https://doi.org/10.1186/s13256-022-03701-3
[ "endovascular", "stroke", "diffusion", "imaging", "flair", "infarction", "intracranial", "hemorrhage", "possible", "weighted" ]
[ { "code": "2F72.Y", "title": "Other specified neoplasms of uncertain behaviour of skin" }, { "code": "BB40/1A62.1", "title": "Acute or subacute infectious endocarditis [Cardiovascular late syphilis]" }, { "code": "8B20", "title": "Stroke not known if ischaemic or haemorrhagic" }, { "code": "8B11.5Z", "title": "Cerebral ischaemic stroke, unspecified" }, { "code": "JB64.4", "title": "Diseases of the circulatory system complicating pregnancy, childbirth or the puerperium" }, { "code": "8B11.2Z", "title": "Cerebral ischaemic stroke due to embolic occlusion, unspecified" }, { "code": "8B25.4", "title": "Late effects of stroke not known if ischaemic or haemorrhagic" }, { "code": "8A40.Y", "title": "Other specified multiple sclerosis" }, { "code": "FB32.Y", "title": "Other specified disorders of muscles" }, { "code": "4A42.1", "title": "Diffuse systemic sclerosis" } ]
=== ICD-11 CODES FOUND === [2F72.Y] Other specified neoplasms of uncertain behaviour of skin Also known as: Other specified neoplasms of uncertain behaviour of skin | Atypical fibroxanthoma | Kaposiform haemangioendothelioma | Basal cell tumour of unspecified site | Composite haemangioendothelioma of unspecified site [8B20] Stroke not known if ischaemic or haemorrhagic Definition: Fulfills criteria for stroke in acute symptoms of focal brain injury that have lasted 24 hours or more (or led to death before 24 hours), but subtype of stroke (ischemic or haemorrhagic) has not been determined by neuroimaging or other techniques. Also known as: Stroke not known if ischaemic or haemorrhagic | apoplexy | brain vascular accident | cerebral accident | cerebral apoplexy Excludes: sequelae of stroke [8B11.5Z] Cerebral ischaemic stroke, unspecified Also known as: Cerebral ischaemic stroke, unspecified | Cerebral ischaemic stroke of unknown cause | cryptogenic stroke | occlusion and stenosis of cerebral and precerebral arteries, resulting in cerebral infarction | cerebral infarct [JB64.4] Diseases of the circulatory system complicating pregnancy, childbirth or the puerperium Also known as: Diseases of the circulatory system complicating pregnancy, childbirth or the puerperium | Spontaneous coronary artery dissection complicating pregnancy, childbirth or the puerperium | Cerebrovascular disorder in the puerperium | puerperal cerebrovascular disease | Acute puerperal cerebrovascular disease Excludes: Obstetric embolism | venous complications and cerebrovenous sinus thrombosis in pregnancy | Venous complications in the puerperium [8B11.2Z] Cerebral ischaemic stroke due to embolic occlusion, unspecified Also known as: Cerebral ischaemic stroke due to embolic occlusion, unspecified | Cerebral ischaemic stroke due to embolic occlusion | cerebral infarction due to embolic occlusion | embolic stroke NOS | Embolic stroke of undermined source [8B25.4] Late effects of stroke not known if ischaemic or haemorrhagic Definition: Late effects occurring 1 month or later after the onset of the disease. Codes for acute stroke should be exclusively used for the acute stroke and immediately related hospitalisation episodes. Also known as: Late effects of stroke not known if ischaemic or haemorrhagic | sequelae of stroke, not specified as haemorrhage or infarction | old cerebrovascular accident | old CVA - [cerebrovascular accident] | old stroke [8A40.Y] Other specified multiple sclerosis Also known as: Other specified multiple sclerosis | Certain specified rare variants of multiple sclerosis | Multiple sclerosis, Marburg variant | Myelinoclastic diffuse sclerosis | Schilder disease [FB32.Y] Other specified disorders of muscles Also known as: Other specified disorders of muscles | Muscle wasting or atrophy, not elsewhere classified | muscle wasting | muscle wasting disorder | Sarcopenia [4A42.1] Diffuse systemic sclerosis Definition: Diffuse cutaneous systemic sclerosis (dcSSc) is a subtype of Systemic Sclerosis (SSc) characterised by truncal and acral skin fibrosis with an early and significant incidence of diffuse involvement (interstitial lung disease, oliguric renal failure, diffuse gastrointestinal disease, and myocardial involvement). Also known as: Diffuse systemic sclerosis | Progressive systemic sclerosis === GRAPH WALKS === --- Walk 1 --- [2F72.Y] Other specified neoplasms of uncertain behaviour of skin --PARENT--> [2F72] Neoplasms of uncertain behaviour of skin --CHILD--> [2F72.2] Melanocytic naevus with severe melanocytic dysplasia Def: Melanocytic naevus with severe melanocytic dysplasia is a histopathological diagnosis based on the presence of severe cytological atypia, defined as enlarged, spindle- and epithelioid-shaped melanocyt... --- Walk 2 --- [2F72.Y] Other specified neoplasms of uncertain behaviour of skin --PARENT--> [2F72] Neoplasms of uncertain behaviour of skin --CHILD--> [2F72.2] Melanocytic naevus with severe melanocytic dysplasia Def: Melanocytic naevus with severe melanocytic dysplasia is a histopathological diagnosis based on the presence of severe cytological atypia, defined as enlarged, spindle- and epithelioid-shaped melanocyt... --- Walk 3 --- [8B20] Stroke not known if ischaemic or haemorrhagic Def: Fulfills criteria for stroke in acute symptoms of focal brain injury that have lasted 24 hours or more (or led to death before 24 hours), but subtype of stroke (ischemic or haemorrhagic) has not been ... --EXCLUDES--> [?] Late effects of stroke not known if ischaemic or haemorrhagic Def: Late effects occurring 1 month or later after the onset of the disease. Codes for acute stroke should be exclusively used for the acute stroke and immediately related hospitalisation episodes.... --PARENT--> [?] Late effects of cerebrovascular disease Def: Effects of cerebrovascular disease 1 month or later after the onset of the disease. Codes for acute stroke should be exclusively used for the acute stroke and immediately related hospitalisation episo... --- Walk 4 --- [8B20] Stroke not known if ischaemic or haemorrhagic Def: Fulfills criteria for stroke in acute symptoms of focal brain injury that have lasted 24 hours or more (or led to death before 24 hours), but subtype of stroke (ischemic or haemorrhagic) has not been ... --EXCLUDES--> [?] Late effects of stroke not known if ischaemic or haemorrhagic Def: Late effects occurring 1 month or later after the onset of the disease. Codes for acute stroke should be exclusively used for the acute stroke and immediately related hospitalisation episodes.... --PARENT--> [?] Late effects of cerebrovascular disease Def: Effects of cerebrovascular disease 1 month or later after the onset of the disease. Codes for acute stroke should be exclusively used for the acute stroke and immediately related hospitalisation episo... --- Walk 5 --- [8B11.5Z] Cerebral ischaemic stroke, unspecified --PARENT--> [8B11.5] Cerebral ischaemic stroke of unknown cause Def: This is a sudden loss of brain function due to a lack of adequate blood flow. It is of an uncertain nature, and approximately 30% of examined events fall into this category.... --CHILD--> [8B11.5Z] Cerebral ischaemic stroke, unspecified --- Walk 6 --- [8B11.5Z] Cerebral ischaemic stroke, unspecified --PARENT--> [8B11.5] Cerebral ischaemic stroke of unknown cause Def: This is a sudden loss of brain function due to a lack of adequate blood flow. It is of an uncertain nature, and approximately 30% of examined events fall into this category.... --CHILD--> [8B11.51] Cerebral ischaemic stroke due to unspecified occlusion or stenosis of intracranial large artery Def: This is a sudden loss of brain function due to a lack of adequate blood flow of the large intracranial arteries....
[ "[2F72.Y] Other specified neoplasms of uncertain behaviour of skin\n --PARENT--> [2F72] Neoplasms of uncertain behaviour of skin\n --CHILD--> [2F72.2] Melanocytic naevus with severe melanocytic dysplasia\n Def: Melanocytic naevus with severe melanocytic dysplasia is a histopathological diagnosis based on the presence of severe cytological atypia, defined as enlarged, spindle- and epithelioid-shaped melanocyt...", "[2F72.Y] Other specified neoplasms of uncertain behaviour of skin\n --PARENT--> [2F72] Neoplasms of uncertain behaviour of skin\n --CHILD--> [2F72.2] Melanocytic naevus with severe melanocytic dysplasia\n Def: Melanocytic naevus with severe melanocytic dysplasia is a histopathological diagnosis based on the presence of severe cytological atypia, defined as enlarged, spindle- and epithelioid-shaped melanocyt...", "[8B20] Stroke not known if ischaemic or haemorrhagic\n Def: Fulfills criteria for stroke in acute symptoms of focal brain injury that have lasted 24 hours or more (or led to death before 24 hours), but subtype of stroke (ischemic or haemorrhagic) has not been ...\n --EXCLUDES--> [?] Late effects of stroke not known if ischaemic or haemorrhagic\n Def: Late effects occurring 1 month or later after the onset of the disease. Codes for acute stroke should be exclusively used for the acute stroke and immediately related hospitalisation episodes....\n --PARENT--> [?] Late effects of cerebrovascular disease\n Def: Effects of cerebrovascular disease 1 month or later after the onset of the disease. Codes for acute stroke should be exclusively used for the acute stroke and immediately related hospitalisation episo...", "[8B20] Stroke not known if ischaemic or haemorrhagic\n Def: Fulfills criteria for stroke in acute symptoms of focal brain injury that have lasted 24 hours or more (or led to death before 24 hours), but subtype of stroke (ischemic or haemorrhagic) has not been ...\n --EXCLUDES--> [?] Late effects of stroke not known if ischaemic or haemorrhagic\n Def: Late effects occurring 1 month or later after the onset of the disease. Codes for acute stroke should be exclusively used for the acute stroke and immediately related hospitalisation episodes....\n --PARENT--> [?] Late effects of cerebrovascular disease\n Def: Effects of cerebrovascular disease 1 month or later after the onset of the disease. Codes for acute stroke should be exclusively used for the acute stroke and immediately related hospitalisation episo...", "[8B11.5Z] Cerebral ischaemic stroke, unspecified\n --PARENT--> [8B11.5] Cerebral ischaemic stroke of unknown cause\n Def: This is a sudden loss of brain function due to a lack of adequate blood flow. It is of an uncertain nature, and approximately 30% of examined events fall into this category....\n --CHILD--> [8B11.5Z] Cerebral ischaemic stroke, unspecified", "[8B11.5Z] Cerebral ischaemic stroke, unspecified\n --PARENT--> [8B11.5] Cerebral ischaemic stroke of unknown cause\n Def: This is a sudden loss of brain function due to a lack of adequate blood flow. It is of an uncertain nature, and approximately 30% of examined events fall into this category....\n --CHILD--> [8B11.51] Cerebral ischaemic stroke due to unspecified occlusion or stenosis of intracranial large artery\n Def: This is a sudden loss of brain function due to a lack of adequate blood flow of the large intracranial arteries...." ]
2F72.Y
Other specified neoplasms of uncertain behaviour of skin
[ { "from_icd11": "2F72.Y", "icd10_code": "D485", "icd10_title": "Neoplasm of uncertain behavior of skin" }, { "from_icd11": "8B20", "icd10_code": "I64", "icd10_title": "" }, { "from_icd11": "JB64.4", "icd10_code": "O9942", "icd10_title": "Diseases of the circulatory system complicating childbirth" }, { "from_icd11": "JB64.4", "icd10_code": "O9943", "icd10_title": "Diseases of the circulatory system complicating the puerperium" }, { "from_icd11": "JB64.4", "icd10_code": "O99411", "icd10_title": "Diseases of the circulatory system complicating pregnancy, first trimester" }, { "from_icd11": "JB64.4", "icd10_code": "O99412", "icd10_title": "Diseases of the circulatory system complicating pregnancy, second trimester" }, { "from_icd11": "JB64.4", "icd10_code": "O99413", "icd10_title": "Diseases of the circulatory system complicating pregnancy, third trimester" }, { "from_icd11": "JB64.4", "icd10_code": "O994", "icd10_title": "Diseases of the circulatory system complicating pregnancy, childbirth and the puerperium" }, { "from_icd11": "8B11.2Z", "icd10_code": "I63412", "icd10_title": "Cerebral infarction due to embolism of left middle cerebral artery" }, { "from_icd11": "8B11.2Z", "icd10_code": "I6340", "icd10_title": "Cerebral infarction due to embolism of unspecified cerebral artery" }, { "from_icd11": "8B11.2Z", "icd10_code": "I6310", "icd10_title": "Cerebral infarction due to embolism of unspecified precerebral artery" }, { "from_icd11": "8B11.2Z", "icd10_code": "I63449", "icd10_title": "Cerebral infarction due to embolism of unspecified cerebellar artery" }, { "from_icd11": "8B11.2Z", "icd10_code": "I63421", "icd10_title": "Cerebral infarction due to embolism of right anterior cerebral artery" }, { "from_icd11": "8B11.2Z", "icd10_code": "I6312", "icd10_title": "Cerebral infarction due to embolism of basilar artery" }, { "from_icd11": "8B11.2Z", "icd10_code": "I63132", "icd10_title": "Cerebral infarction due to embolism of left carotid artery" } ]
D485
Neoplasm of uncertain behavior of skin
A 71-year-old Japanese woman presented to our hospital with high fever and severe cough, and was admitted for bacterial pneumonia. Before her admission, she had developed fever and cough, and had received treatment with the anti-inflammatory drug loxoprofen. However, her symptoms deteriorated. Her initial vital signs on admission were as follows: temperature, 37.8 °C; respiratory rate, 18 breaths/minute; and oxygen saturation (SpO 2 ) on room air, 94 %. A physical examination revealed fine crackles in both her lower lung fields. Her laboratory test values were as follows: white blood cell (WBC) count, 6000/μL; neutrophil count, 3780/μL; serum lactate dehydrogenase (LDH) level, 230 IU/L (normal, 119 to 229 IU/L); and serum C-reactive protein (CRP) level, 6.3 mg/dL (normal, <0.3 mg/dL). A chest radiograph showed reticular shadows in both her lower lung fields. Chest computed tomography showed consolidation. A sputum Gram stain revealed only normal bacterial flora. Mycoplasma antigen was absent. Urinary antigen tests for Legionella and Streptococcus pneumoniae also yielded negative results. Fig. 1 Chest X-ray images. a Chest X-ray on admission. b Chest X-ray at the time of worsening of respiratory failure. c Chest X-ray after steroid treatment Fig. 2 Chest computed tomography images. a Chest computed tomography on admission. b Chest computed tomography at the time of worsening of respiratory failure
3.8125
0.981445
sec[1]/p[0]
en
0.999995
27225339
https://doi.org/10.1186/s13256-016-0919-2
[ "chest", "computed", "tomography", "respiratory", "fever", "cough", "bacterial", "follows", "both", "lung" ]
[ { "code": "CB7Z", "title": "Diseases of the respiratory system, unspecified" }, { "code": "CB27", "title": "Pleural effusion" }, { "code": "CA44", "title": "Pyothorax" }, { "code": "MD30.Z", "title": "Chest pain, unspecified" }, { "code": "NA80.Y&XJ1C6", "title": "Thoracic haematoma" }, { "code": "CB41", "title": "Respiratory failure" }, { "code": "CB41.2Z", "title": "Respiratory failure, unspecified" }, { "code": "CB40.Y", "title": "Other specified diseases of the respiratory system" }, { "code": "MD11.Y", "title": "Other specified abnormalities of breathing" }, { "code": "MG26", "title": "Fever of other or unknown origin" } ]
=== ICD-11 CODES FOUND === [CB7Z] Diseases of the respiratory system, unspecified Also known as: Diseases of the respiratory system, unspecified | disorder of respiratory system | respiratory disease NOS | respiratory tract disease | respiratory disorder NOS [CB27] Pleural effusion Definition: Presence of fluid in the pleural cavity resulting from excessive transudation or exudation from the pleural surfaces. Also known as: Pleural effusion | PE - [pleural effusion] | Pleurisy with effusion | pleurisy with effusion NOS | pleural effusion with transudate Includes: Pleurisy with effusion Excludes: Tuberculosis of the respiratory system | Chylous effusion | Pleurisy [CA44] Pyothorax Definition: Suppurative inflammation of the pleural space, typically due to acute bacterial infection. It can occur as a complication of pneumonia, thoracotomy, abscesses (lung, hepatic, or subdiaphragmatic), or penetrating trauma with a secondary infection. Also known as: Pyothorax | empyema | pyopneumothorax | Pyothorax with fistula | empyema with fistula Includes: empyema | pyopneumothorax Excludes: due to tuberculosis [MD30.Z] Chest pain, unspecified Also known as: Chest pain, unspecified | Pain in throat or chest | chest pain NOS | pain in chest | chest pressure [CB41] Respiratory failure Definition: Respiratory failure is a life-threatening impairment of oxygenation or carbon dioxide (CO2) elimination. Respiratory failure may occur because of impaired gas exchange, decreased ventilation, or both. The level of oxygen in the blood becomes dangerously low or the level of carbon dioxide becomes dangerously high. Also known as: Respiratory failure | lung failure NOS | pulmonary failure Excludes: Acute respiratory distress syndrome | Respiratory arrest | Respiratory distress of newborn [CB41.2Z] Respiratory failure, unspecified Also known as: Respiratory failure, unspecified | Respiratory failure, unspecified as acute or chronic | respiration failure | respiratory failure NOS | respiration failed [CB40.Y] Other specified diseases of the respiratory system Also known as: Other specified diseases of the respiratory system | Secondary respiratory disorders | Respiratory disorders in diseases classified elsewhere | Diseases of bronchus, not elsewhere classified | Acquired bronchial diverticulum [MD11.Y] Other specified abnormalities of breathing Also known as: Other specified abnormalities of breathing | Bradypnoea | Choking sensation | Hypoventilation | hypoventilation syndrome NOS [MG26] Fever of other or unknown origin Definition: An abnormal elevation of body temperature of unknown origin, often as a result of a pathologic process. Also known as: Fever of other or unknown origin | febrile | febris | fever | feverish Excludes: fever of unknown origin in newborn | Malignant hyperthermia due to anaesthesia === GRAPH WALKS === --- Walk 1 --- [CB7Z] Diseases of the respiratory system, unspecified --PARENT--> [12] Diseases of the respiratory system --CHILD--> [?] Upper respiratory tract disorders Def: This group of disorders refers to diseases of the upper airways (upper respiratory tract). The upper airways anatomically are complicated structures which extend from the airway openings at the nares ... --- Walk 2 --- [CB7Z] Diseases of the respiratory system, unspecified --PARENT--> [12] Diseases of the respiratory system --CHILD--> [?] Certain lower respiratory tract diseases Def: This group refers to diseases of airways that forms the connection between the outside world and the terminal respiratory unit. Intrapulmonary airways are divided into three major groups; bronchi, mem... --- Walk 3 --- [CB27] Pleural effusion Def: Presence of fluid in the pleural cavity resulting from excessive transudation or exudation from the pleural surfaces.... --EXCLUDES--> [?] Chylous effusion Def: A chylothorax (chylous effusion) signifies leakage of chyle from the thoracic duct. A pleural fluid triglyceride concentration of more than 110 mg per decilitre signifies a high likelihood of chylotho... --PARENT--> [?] Other pleural conditions Def: Any other condition effecting the thin serous membrane enveloping the lungs and lining the thoracic cavity... --- Walk 4 --- [CB27] Pleural effusion Def: Presence of fluid in the pleural cavity resulting from excessive transudation or exudation from the pleural surfaces.... --EXCLUDES--> [?] Tuberculosis of the respiratory system Def: This is a progressive or chronic disease resulting from infection with the bacterium Mycobacterium tuberculosis or other bacteria in the M. tuberculosis complex: M. bovis, M. africanum, M. canetti, M.... --CHILD--> [?] Tuberculosis of lung, without mention of bacteriological or histological confirmation Def: This is a common, and in many cases lethal, infectious disease of the lung caused by various strains of mycobacteria, usually Mycobacterium tuberculosis. This diagnosis is without mention of bacteriol... --- Walk 5 --- [CA44] Pyothorax Def: Suppurative inflammation of the pleural space, typically due to acute bacterial infection. It can occur as a complication of pneumonia, thoracotomy, abscesses (lung, hepatic, or subdiaphragmatic), or ... --PARENT--> [?] Lung infections Def: Any condition of the lungs, caused by an infection with a bacterial, viral, fungal, or parasitic source.... --RELATED_TO--> [?] Chronic obstructive pulmonary disease with acute lower respiratory infection Def: Chronic obstructive pulmonary disease (COPD) with a lower respiratory tract infection usually caused by a virus or bacteria.... --- Walk 6 --- [CA44] Pyothorax Def: Suppurative inflammation of the pleural space, typically due to acute bacterial infection. It can occur as a complication of pneumonia, thoracotomy, abscesses (lung, hepatic, or subdiaphragmatic), or ... --EXCLUDES--> [?] Tuberculous pleurisy, without mention of bacteriological or histological confirmation Def: This is a common, and in many cases lethal, infectious disease caused by various strains of mycobacteria, usually Mycobacterium tuberculosis, with an inflammation of the pleura. This diagnosis is with... --CHILD--> [?] Tuberculous empyema, without mention of bacteriological or histological confirmation
[ "[CB7Z] Diseases of the respiratory system, unspecified\n --PARENT--> [12] Diseases of the respiratory system\n --CHILD--> [?] Upper respiratory tract disorders\n Def: This group of disorders refers to diseases of the upper airways (upper respiratory tract). The upper airways anatomically are complicated structures which extend from the airway openings at the nares ...", "[CB7Z] Diseases of the respiratory system, unspecified\n --PARENT--> [12] Diseases of the respiratory system\n --CHILD--> [?] Certain lower respiratory tract diseases\n Def: This group refers to diseases of airways that forms the connection between the outside world and the terminal respiratory unit. Intrapulmonary airways are divided into three major groups; bronchi, mem...", "[CB27] Pleural effusion\n Def: Presence of fluid in the pleural cavity resulting from excessive transudation or exudation from the pleural surfaces....\n --EXCLUDES--> [?] Chylous effusion\n Def: A chylothorax (chylous effusion) signifies leakage of chyle from the thoracic duct. A pleural fluid triglyceride concentration of more than 110 mg per decilitre signifies a high likelihood of chylotho...\n --PARENT--> [?] Other pleural conditions\n Def: Any other condition effecting the thin serous membrane enveloping the lungs and lining the thoracic cavity...", "[CB27] Pleural effusion\n Def: Presence of fluid in the pleural cavity resulting from excessive transudation or exudation from the pleural surfaces....\n --EXCLUDES--> [?] Tuberculosis of the respiratory system\n Def: This is a progressive or chronic disease resulting from infection with the bacterium Mycobacterium tuberculosis or other bacteria in the M. tuberculosis complex: M. bovis, M. africanum, M. canetti, M....\n --CHILD--> [?] Tuberculosis of lung, without mention of bacteriological or histological confirmation\n Def: This is a common, and in many cases lethal, infectious disease of the lung caused by various strains of mycobacteria, usually Mycobacterium tuberculosis. This diagnosis is without mention of bacteriol...", "[CA44] Pyothorax\n Def: Suppurative inflammation of the pleural space, typically due to acute bacterial infection. It can occur as a complication of pneumonia, thoracotomy, abscesses (lung, hepatic, or subdiaphragmatic), or ...\n --PARENT--> [?] Lung infections\n Def: Any condition of the lungs, caused by an infection with a bacterial, viral, fungal, or parasitic source....\n --RELATED_TO--> [?] Chronic obstructive pulmonary disease with acute lower respiratory infection\n Def: Chronic obstructive pulmonary disease (COPD) with a lower respiratory tract infection usually caused by a virus or bacteria....", "[CA44] Pyothorax\n Def: Suppurative inflammation of the pleural space, typically due to acute bacterial infection. It can occur as a complication of pneumonia, thoracotomy, abscesses (lung, hepatic, or subdiaphragmatic), or ...\n --EXCLUDES--> [?] Tuberculous pleurisy, without mention of bacteriological or histological confirmation\n Def: This is a common, and in many cases lethal, infectious disease caused by various strains of mycobacteria, usually Mycobacterium tuberculosis, with an inflammation of the pleura. This diagnosis is with...\n --CHILD--> [?] Tuberculous empyema, without mention of bacteriological or histological confirmation" ]
CB7Z
Diseases of the respiratory system, unspecified
[ { "from_icd11": "CB7Z", "icd10_code": "J989", "icd10_title": "Respiratory disorder, unspecified" }, { "from_icd11": "CB7Z", "icd10_code": "X", "icd10_title": "" }, { "from_icd11": "CB7Z", "icd10_code": "J09-J18", "icd10_title": "" }, { "from_icd11": "CB27", "icd10_code": "J910", "icd10_title": "Malignant pleural effusion" }, { "from_icd11": "CB27", "icd10_code": "J918", "icd10_title": "Pleural effusion in other conditions classified elsewhere" }, { "from_icd11": "CB27", "icd10_code": "J90", "icd10_title": "Pleural effusion, not elsewhere classified" }, { "from_icd11": "CB27", "icd10_code": "J90-J94", "icd10_title": "" }, { "from_icd11": "CB27", "icd10_code": "J91", "icd10_title": "Pleural effusion in conditions classified elsewhere" }, { "from_icd11": "CA44", "icd10_code": "J869", "icd10_title": "Pyothorax without fistula" }, { "from_icd11": "CA44", "icd10_code": "J860", "icd10_title": "Pyothorax with fistula" }, { "from_icd11": "CA44", "icd10_code": "J85-J86", "icd10_title": "" }, { "from_icd11": "CA44", "icd10_code": "J86", "icd10_title": "Pyothorax" }, { "from_icd11": "MD30.Z", "icd10_code": "R0781", "icd10_title": "Pleurodynia" }, { "from_icd11": "MD30.Z", "icd10_code": "R0782", "icd10_title": "Intercostal pain" }, { "from_icd11": "MD30.Z", "icd10_code": "R079", "icd10_title": "Chest pain, unspecified" } ]
J989
Respiratory disorder, unspecified
Fluorescein angiography showed hyperfluorescence corresponding to the peripheral whitening with perivascular leakage in the left eye and optic disc leakage in both eyes . B-scan of the superonasal quadrant did not reveal a corresponding elevation or abnormality . OCT of the lesion revealed retinal infiltration with hyperreflective dots . Figure 2 Fluorescein angiography of the left and right eyes. (A) Fluorescein angiography of the left eye: early hyperfluorescence corresponding to the area of retinal whitening and haziness. (B) Fluorescein angiography of the left eye: late frame shows perivascular leakage in the same area (vasculitis) together with late hyperfluorescence of the disc. (C) Fluorescein angiography of the right eye: late hyperfluorescence and leakage from the disc. Figure 3 B-scan ultrasound of the right and left eyes. (A) B-scan ultrasound of the right eye: elevation of optic nerve head. (B) B-scan ultrasound of the left eye: no visible elevation could be appreciated in the superonasal quadrant of the left eye. Figure 4 OCT of the lesion: irregular retinal contour with areas of retinal elevation. The individual retinal layers could not be distinguished due to infiltration with multiple hyperreflective dots. Diffuse thickening at the retinal nerve fiber layer. Irregular vitreo-retinal interface with traction by partial PVD together with moderate hyperreflective dots in the vitreous.
3.935547
0.778809
sec[0]/sec[0]/p[2]
en
0.999996
26069511
https://doi.org/10.1186/s12348-015-0045-0
[ "retinal", "fluorescein", "angiography", "hyperfluorescence", "leakage", "scan", "elevation", "corresponding", "disc", "eyes" ]
[ { "code": "9B7Z", "title": "Disorders of the retina, unspecified" }, { "code": "9B74.Z", "title": "Retinal vascular occlusions, unspecified" }, { "code": "9B73.4", "title": "Retinal breaks without detachment" }, { "code": "9B78.9", "title": "Retinal atrophy" }, { "code": "9B7Y", "title": "Other specified disorders of the retina" }, { "code": "CB21.Z", "title": "Pneumothorax, unspecified" }, { "code": "MF50.5", "title": "Extravasation of urine" }, { "code": "NE81.3", "title": "Postsurgical leak" }, { "code": "GB0Y", "title": "Other specified diseases of the male genital system" }, { "code": "CB60", "title": "Tracheostomy malfunction" } ]
=== ICD-11 CODES FOUND === [9B7Z] Disorders of the retina, unspecified Also known as: Disorders of the retina, unspecified | retinal disease | retinal lesion NOS [9B74.Z] Retinal vascular occlusions, unspecified Also known as: Retinal vascular occlusions, unspecified | Retinal vascular occlusions | occlusion of retinal vessels | retinal obstruction [9B73.4] Retinal breaks without detachment Also known as: Retinal breaks without detachment | Retinal break NOS | ruptured retina | Horseshoe tear of retina without detachment | Round hole of retina without detachment Includes: Horseshoe tear of retina without detachment | Round hole of retina without detachment Excludes: Chorioretinal scars after surgery for detachment | peripheral retinal degeneration without break [9B78.9] Retinal atrophy Definition: This is a group of genetic diseases and is characterised by the bilateral degeneration of the retina, causing progressive vision loss culminating in blindness. Also known as: Retinal atrophy | atrophic retina [9B7Y] Other specified disorders of the retina Also known as: Other specified disorders of the retina | Åland Island eye disease | Cone dystrophy with supernormal rod response | Familial retinal arterial macroaneurysm | IRVAN syndrome [CB21.Z] Pneumothorax, unspecified Also known as: Pneumothorax, unspecified | Pneumothorax | pneumothorax NOS | air leak NOS | pleural air leak NOS [MF50.5] Extravasation of urine Also known as: Extravasation of urine | leakage of urine | Rupture of a renal calyx | Rupture of a renal fornix [NE81.3] Postsurgical leak Also known as: Postsurgical leak | postoperative leak | Postsurgical air leak | postoperative air leak | Postsurgical bile leak Excludes: Malfunction or complication of external stoma of digestive organs | Tracheostomy malfunction [GB0Y] Other specified diseases of the male genital system Also known as: Other specified diseases of the male genital system | Diseases of male genital organs | disease or disorder of male genitourinary system | Pain in scrotum | scrotal pain [CB60] Tracheostomy malfunction Also known as: Tracheostomy malfunction | tracheostomy dysfunction | status of malfunctioning tracheostomy | functional disturbance of tracheostomy | tracheostomy complications === GRAPH WALKS === --- Walk 1 --- [9B7Z] Disorders of the retina, unspecified --PARENT--> [?] Disorders of the retina --RELATED_TO--> [?] Neoplasms of retina Def: This refers to tumours of the light-sensitive layer of tissue, lining the inner surface of the eye. The optics of the eye create an image of the visual world on the retina, which serves much the same ... --- Walk 2 --- [9B7Z] Disorders of the retina, unspecified --PARENT--> [?] Disorders of the retina --RELATED_TO--> [?] Traumatic injuries of the retina Def: This refers to traumatic injuries of the light-sensitive layer of tissue, lining the inner surface of the eye. The optics of the eye create an image of the visual world on the retina, which serves muc... --- Walk 3 --- [9B74.Z] Retinal vascular occlusions, unspecified --PARENT--> [9B74] Retinal vascular occlusions Def: These are obstruction or closure of retinal vascular structures.... --CHILD--> [9B74.2] Combined retinal arterial and vein occlusion --- Walk 4 --- [9B74.Z] Retinal vascular occlusions, unspecified --PARENT--> [9B74] Retinal vascular occlusions Def: These are obstruction or closure of retinal vascular structures.... --PARENT--> [?] Disorders of the retina --- Walk 5 --- [9B73.4] Retinal breaks without detachment --EXCLUDES--> [?] Chorioretinal scars after surgery for detachment --PARENT--> [?] Postprocedural disorders of eye or ocular adnexa --- Walk 6 --- [9B73.4] Retinal breaks without detachment --EXCLUDES--> [?] Peripheral retinal degeneration --CHILD--> [?] Paving stone degeneration of retina
[ "[9B7Z] Disorders of the retina, unspecified\n --PARENT--> [?] Disorders of the retina\n --RELATED_TO--> [?] Neoplasms of retina\n Def: This refers to tumours of the light-sensitive layer of tissue, lining the inner surface of the eye. The optics of the eye create an image of the visual world on the retina, which serves much the same ...", "[9B7Z] Disorders of the retina, unspecified\n --PARENT--> [?] Disorders of the retina\n --RELATED_TO--> [?] Traumatic injuries of the retina\n Def: This refers to traumatic injuries of the light-sensitive layer of tissue, lining the inner surface of the eye. The optics of the eye create an image of the visual world on the retina, which serves muc...", "[9B74.Z] Retinal vascular occlusions, unspecified\n --PARENT--> [9B74] Retinal vascular occlusions\n Def: These are obstruction or closure of retinal vascular structures....\n --CHILD--> [9B74.2] Combined retinal arterial and vein occlusion", "[9B74.Z] Retinal vascular occlusions, unspecified\n --PARENT--> [9B74] Retinal vascular occlusions\n Def: These are obstruction or closure of retinal vascular structures....\n --PARENT--> [?] Disorders of the retina", "[9B73.4] Retinal breaks without detachment\n --EXCLUDES--> [?] Chorioretinal scars after surgery for detachment\n --PARENT--> [?] Postprocedural disorders of eye or ocular adnexa", "[9B73.4] Retinal breaks without detachment\n --EXCLUDES--> [?] Peripheral retinal degeneration\n --CHILD--> [?] Paving stone degeneration of retina" ]
9B7Z
Disorders of the retina, unspecified
[ { "from_icd11": "9B7Z", "icd10_code": "H30-H36", "icd10_title": "" }, { "from_icd11": "9B7Z", "icd10_code": "H32", "icd10_title": "Chorioretinal disorders in diseases classified elsewhere" }, { "from_icd11": "9B7Z", "icd10_code": "H320", "icd10_title": "" }, { "from_icd11": "9B7Z", "icd10_code": "H328", "icd10_title": "" }, { "from_icd11": "9B74.Z", "icd10_code": "H348192", "icd10_title": "Central retinal vein occlusion, unspecified eye, stable" }, { "from_icd11": "9B74.Z", "icd10_code": "H348310", "icd10_title": "Tributary (branch) retinal vein occlusion, right eye, with macular edema" }, { "from_icd11": "9B74.Z", "icd10_code": "H348112", "icd10_title": "Central retinal vein occlusion, right eye, stable" }, { "from_icd11": "9B74.Z", "icd10_code": "H348122", "icd10_title": "Central retinal vein occlusion, left eye, stable" }, { "from_icd11": "9B74.Z", "icd10_code": "H34819", "icd10_title": "Central retinal vein occlusion, unspecified eye" }, { "from_icd11": "9B74.Z", "icd10_code": "H348392", "icd10_title": "Tributary (branch) retinal vein occlusion, unspecified eye, stable" }, { "from_icd11": "9B74.Z", "icd10_code": "H34812", "icd10_title": "Central retinal vein occlusion, left eye" }, { "from_icd11": "9B74.Z", "icd10_code": "H34813", "icd10_title": "Central retinal vein occlusion, bilateral" }, { "from_icd11": "9B74.Z", "icd10_code": "H348120", "icd10_title": "Central retinal vein occlusion, left eye, with macular edema" }, { "from_icd11": "9B74.Z", "icd10_code": "H348320", "icd10_title": "Tributary (branch) retinal vein occlusion, left eye, with macular edema" }, { "from_icd11": "9B74.Z", "icd10_code": "H34811", "icd10_title": "Central retinal vein occlusion, right eye" } ]
H30-H36
Marfan syndrome is an autosomal dominant disorder of the connective tissue predisposing to aortic aneurism and caused by mutations in the fibrillin-1 ( FBN1 ) gene on chromosome 15q21.1. A couple, in which the father is affected by Marfan syndrome and has had an aorta replacement and treatment for a detached retina, requested preimplantation genetic diagnosis (PGD). The father was previously referred to us by an accredited National Health Service (NHS) laboratory as heterozygous for two mutations in FBN1 , c.235C>T and c.3089A>G. The first, c.235C>T (p.Gln79X) is a nonsense change that has been reported in the FBN1 online mutation database http://www.umd.be/FBN1/4DACTION/WV/2699 . The second variant is a missense change c.3089A>G , this was not reported in the database at the time of writing. While the database does not assign specific pathologies to each mutation, the reasonable assumption was made that one or both of these mutations in FBN1 were the cause of Marfan Syndrome in this patient. While there was no molecular work up of older family members there was also no prior family history of the syndrome. Both were found to be present in his affected daughter (5 years old at the time of treatment) establishing that they are present in cis on the same paternal chromosome. The mother (36 years old at the time of treatment) had only one other natural pregnancy that resulted in a hydatidiform mole.
4.171875
0.520508
sec[1]/sec[0]/p[0]
en
0.999998
25561157
https://doi.org/10.1007/s10815-014-0405-y
[ "that", "marfan", "mutations", "database", "time", "chromosome", "father", "affected", "change", "mutation" ]
[ { "code": "8A80.Z", "title": "Migraine, unspecified" }, { "code": "QA76", "title": "Medication or substance that is known to be an allergen without injury or harm" }, { "code": "PL13.6", "title": "Medication or substance that is known to be an allergen, as mode of injury or harm" }, { "code": "9C40.A0", "title": "Papilloedema" }, { "code": "PA6Z", "title": "Unintentional fall from unspecified height" }, { "code": "LD28.01", "title": "Marfan syndrome" }, { "code": "LD28.0Z", "title": "Marfan syndrome or Marfan-related disorders, unspecified" }, { "code": "LD28.0Y", "title": "Other specified Marfan syndrome or Marfan-related disorders" }, { "code": "QA0A.6", "title": "Special screening examination for cardiovascular disorders" }, { "code": "GB90.4A", "title": "Nephrogenic diabetes insipidus" } ]
=== ICD-11 CODES FOUND === [8A80.Z] Migraine, unspecified Also known as: Migraine, unspecified | Migraine [QA76] Medication or substance that is known to be an allergen without injury or harm Definition: Medication that has previously been identified as an allergen to the patient is administered, but does not result in injury or harm. Also known as: Medication or substance that is known to be an allergen without injury or harm Excludes: Medication or substance that is known to be an allergen, as mode of injury or harm [PL13.6] Medication or substance that is known to be an allergen, as mode of injury or harm Also known as: Medication or substance that is known to be an allergen, as mode of injury or harm | medication error relating to known allergy to drug or substance | adverse drug event relating to known allergy to drug or substance [9C40.A0] Papilloedema Definition: Optic disc swelling that results from increased intracranial pressure Also known as: Papilloedema | Optic disc swelling that results from increased intracranial pressure Includes: Optic disc swelling that results from increased intracranial pressure [PA6Z] Unintentional fall from unspecified height Also known as: Unintentional fall from unspecified height | fall NOS | accidental fall | fall causing injury that resulted in death | fell NOS [LD28.01] Marfan syndrome Definition: Marfan syndrome is a systemic disease of connective tissue characterised by a variable combination of cardiovascular, musculo-skeletal, ophthalmic and pulmonary manifestations. Cardiovascular involvement is characterised by 1) progressive dilation of the aorta accompanied by an increased risk of aortic dissection, which affects prognosis and 2) mitral insufficiency. Skeletal involvement is often the first sign of the disease and can include dolichostenomelia, large size, arachnodactyly, joint hy Also known as: Marfan syndrome | Marfan disease | Marfan syndrome type 1 | Marfan syndrome type 2 | Loeys-Dietz syndrome type 2 [LD28.0Z] Marfan syndrome or Marfan-related disorders, unspecified Also known as: Marfan syndrome or Marfan-related disorders, unspecified | Marfan syndrome or Marfan-related disorders [LD28.0Y] Other specified Marfan syndrome or Marfan-related disorders Also known as: Other specified Marfan syndrome or Marfan-related disorders | Aneurysm - osteoarthritis syndrome | Familial thoracic aortic aneurysm or dissection | Marfanoid craniosynostosis syndrome | Shprintzen-Goldberg [QA0A.6] Special screening examination for cardiovascular disorders Also known as: Special screening examination for cardiovascular disorders | Family screening for Brugada syndrome | Family screening for Long QT syndrome | Screening for Ehlers-Danlos syndrome | Screening for hypertension [GB90.4A] Nephrogenic diabetes insipidus Definition: Nephrogenic diabetes insipidus is a condition in which the kidney tubules respond poorly to pituitary secreted anti-diuretic hormone, resulting in a failure to concentrate the urine, and water loss. Polyuria with dilute urine and polydypsia (excessive thirst) are present. It can be congenital or acquired with many causes. The congenital forms may be attributed to vasopressin receptor or aquaporin-2 defects. They are characterised by polyuria with polydipsia, recurrent bouts of fever, constipatio Also known as: Nephrogenic diabetes insipidus | renal diabetes insipidus | familial nephrogenic diabetes | antidiuretic-hormone-resistant diabetes insipidus | adiuretin-resistant diabetes insipidus Excludes: Central diabetes insipidus === GRAPH WALKS === --- Walk 1 --- [8A80.Z] Migraine, unspecified --PARENT--> [8A80] Migraine Def: A primary headache disorder, in most cases episodic. Disabling attacks lasting 4-72 hours are characterised by moderate or severe headache, usually accompanied by nausea, vomiting and/or photophobia a... --EXCLUDES--> [?] Headache, not elsewhere classified Def: Headache with characteristic features suggesting that it is a unique diagnostic entity, a finding or complaint, but not fulfilling criteria for any of the headache disorders described above.... --- Walk 2 --- [8A80.Z] Migraine, unspecified --PARENT--> [8A80] Migraine Def: A primary headache disorder, in most cases episodic. Disabling attacks lasting 4-72 hours are characterised by moderate or severe headache, usually accompanied by nausea, vomiting and/or photophobia a... --EXCLUDES--> [?] Headache, not elsewhere classified Def: Headache with characteristic features suggesting that it is a unique diagnostic entity, a finding or complaint, but not fulfilling criteria for any of the headache disorders described above.... --- Walk 3 --- [QA76] Medication or substance that is known to be an allergen without injury or harm Def: Medication that has previously been identified as an allergen to the patient is administered, but does not result in injury or harm.... --EXCLUDES--> [?] Medication or substance that is known to be an allergen, as mode of injury or harm --PARENT--> [?] Mode of injury or harm associated with exposure to a drug, medicament or biological substance --- Walk 4 --- [QA76] Medication or substance that is known to be an allergen without injury or harm Def: Medication that has previously been identified as an allergen to the patient is administered, but does not result in injury or harm.... --PARENT--> [?] Circumstances associated with exposure to a drug, medicament or biological substance influencing the episode of care without injury or harm --CHILD--> [QA71] Underdosing without injury or harm Def: Under-dosing occurs when a patient takes less of a medication than is prescribed by the provider or the manufacturer's instructions without documented injury or harm. This can be the result of inaccur... --- Walk 5 --- [PL13.6] Medication or substance that is known to be an allergen, as mode of injury or harm --PARENT--> [PL13] Mode of injury or harm associated with exposure to a drug, medicament or biological substance --CHILD--> [PL13.2] Drug-related injury or harm in the context of correct administration or dosage, as mode of injury or harm --- Walk 6 --- [PL13.6] Medication or substance that is known to be an allergen, as mode of injury or harm --PARENT--> [PL13] Mode of injury or harm associated with exposure to a drug, medicament or biological substance --CHILD--> [PL13.2] Drug-related injury or harm in the context of correct administration or dosage, as mode of injury or harm
[ "[8A80.Z] Migraine, unspecified\n --PARENT--> [8A80] Migraine\n Def: A primary headache disorder, in most cases episodic. Disabling attacks lasting 4-72 hours are characterised by moderate or severe headache, usually accompanied by nausea, vomiting and/or photophobia a...\n --EXCLUDES--> [?] Headache, not elsewhere classified\n Def: Headache with characteristic features suggesting that it is a unique diagnostic entity, a finding or complaint, but not fulfilling criteria for any of the headache disorders described above....", "[8A80.Z] Migraine, unspecified\n --PARENT--> [8A80] Migraine\n Def: A primary headache disorder, in most cases episodic. Disabling attacks lasting 4-72 hours are characterised by moderate or severe headache, usually accompanied by nausea, vomiting and/or photophobia a...\n --EXCLUDES--> [?] Headache, not elsewhere classified\n Def: Headache with characteristic features suggesting that it is a unique diagnostic entity, a finding or complaint, but not fulfilling criteria for any of the headache disorders described above....", "[QA76] Medication or substance that is known to be an allergen without injury or harm\n Def: Medication that has previously been identified as an allergen to the patient is administered, but does not result in injury or harm....\n --EXCLUDES--> [?] Medication or substance that is known to be an allergen, as mode of injury or harm\n --PARENT--> [?] Mode of injury or harm associated with exposure to a drug, medicament or biological substance", "[QA76] Medication or substance that is known to be an allergen without injury or harm\n Def: Medication that has previously been identified as an allergen to the patient is administered, but does not result in injury or harm....\n --PARENT--> [?] Circumstances associated with exposure to a drug, medicament or biological substance influencing the episode of care without injury or harm\n --CHILD--> [QA71] Underdosing without injury or harm\n Def: Under-dosing occurs when a patient takes less of a medication than is prescribed by the provider or the manufacturer's instructions without documented injury or harm. This can be the result of inaccur...", "[PL13.6] Medication or substance that is known to be an allergen, as mode of injury or harm\n --PARENT--> [PL13] Mode of injury or harm associated with exposure to a drug, medicament or biological substance\n --CHILD--> [PL13.2] Drug-related injury or harm in the context of correct administration or dosage, as mode of injury or harm", "[PL13.6] Medication or substance that is known to be an allergen, as mode of injury or harm\n --PARENT--> [PL13] Mode of injury or harm associated with exposure to a drug, medicament or biological substance\n --CHILD--> [PL13.2] Drug-related injury or harm in the context of correct administration or dosage, as mode of injury or harm" ]
8A80.Z
Migraine, unspecified
[ { "from_icd11": "8A80.Z", "icd10_code": "G43B0", "icd10_title": "Ophthalmoplegic migraine, not intractable" }, { "from_icd11": "8A80.Z", "icd10_code": "G43409", "icd10_title": "Hemiplegic migraine, not intractable, without status migrainosus" }, { "from_icd11": "8A80.Z", "icd10_code": "G43A0", "icd10_title": "Cyclical vomiting, in migraine, not intractable" }, { "from_icd11": "8A80.Z", "icd10_code": "G43D0", "icd10_title": "Abdominal migraine, not intractable" }, { "from_icd11": "8A80.Z", "icd10_code": "G43709", "icd10_title": "Chronic migraine without aura, not intractable, without status migrainosus" }, { "from_icd11": "8A80.Z", "icd10_code": "G43A1", "icd10_title": "Cyclical vomiting, in migraine, intractable" }, { "from_icd11": "8A80.Z", "icd10_code": "G43509", "icd10_title": "Persistent migraine aura without cerebral infarction, not intractable, without status migrainosus" }, { "from_icd11": "8A80.Z", "icd10_code": "G43719", "icd10_title": "Chronic migraine without aura, intractable, without status migrainosus" }, { "from_icd11": "8A80.Z", "icd10_code": "G43501", "icd10_title": "Persistent migraine aura without cerebral infarction, not intractable, with status migrainosus" }, { "from_icd11": "8A80.Z", "icd10_code": "G43C0", "icd10_title": "Periodic headache syndromes in child or adult, not intractable" }, { "from_icd11": "8A80.Z", "icd10_code": "G43401", "icd10_title": "Hemiplegic migraine, not intractable, with status migrainosus" }, { "from_icd11": "8A80.Z", "icd10_code": "G43419", "icd10_title": "Hemiplegic migraine, intractable, without status migrainosus" }, { "from_icd11": "8A80.Z", "icd10_code": "G43B1", "icd10_title": "Ophthalmoplegic migraine, intractable" }, { "from_icd11": "8A80.Z", "icd10_code": "G43C1", "icd10_title": "Periodic headache syndromes in child or adult, intractable" }, { "from_icd11": "8A80.Z", "icd10_code": "G43D1", "icd10_title": "Abdominal migraine, intractable" } ]
G43B0
Ophthalmoplegic migraine, not intractable
Patient was admitted for wide excision surgery and reconstruction with Latissimus Dorsi (LD) Flap. Tumor borders were marked. Incision was made 2 cm lateral from tumor borders. Incision deepened through the fascia of biceps brachial muscle. Arteries, veins, median and radial nerve were identified and preserved. The tumor did not infiltrate neurovascular. Wide excision was done. Long and short head biceps brachial muscle, part of brachialis muscle, musculocutaneous nerve and cephalic venous were elevated. Frozen section was performed intra operatively to confirm the margins were negative. Incision was done according to design and deepened to fascia of latissimus dorsi muscle. Latissimus dorsi muscle was elevated while preserving arteries, veins and thoracodorsalis nerve. Flap was put into the defect area. Distal part of latissimus dorsi was sutured to biceps brachii tendon. Medial part was sutured to long and short head of biceps brachii muscle. Surgical wound was sutured layer by layer . Fig. 3 Limb sparing surgery with Latissimus Dorsi (LD) Flap reconstruction in soft tissue sarcoma. A) Incision was made 2 cm lateral from tumor borders and deepened through the fascia. B, C) Arteries, veins, and nerves were identified and preserved. C) Tumor has been removed from the arm. D, E) Flap was put into the defect area. F) Post-operative view of the arm. G) The macroscopic appearance of the tumor. Fig. 3
3.636719
0.978027
sec[1]/p[1]
en
0.999998
35803098
https://doi.org/10.1016/j.ijscr.2022.107345
[ "tumor", "muscle", "latissimus", "dorsi", "flap", "incision", "biceps", "borders", "deepened", "fascia" ]
[ { "code": "2F9Z", "title": "Neoplasms of unknown behaviour of unspecified site" }, { "code": "ME61", "title": "Subcutaneous swelling, mass or lump of uncertain or unspecified nature" }, { "code": "2E6Z", "title": "Carcinoma in situ of unspecified site" }, { "code": "2F91.1", "title": "Neoplasms of unknown behaviour of trachea, bronchus or lung" }, { "code": "2F92", "title": "Neoplasms of unknown behaviour of skin" }, { "code": "FB3Z", "title": "Disorders of muscles, unspecified" }, { "code": "FB32.Y", "title": "Other specified disorders of muscles" }, { "code": "8C70.Z", "title": "Muscular dystrophy, unspecified" }, { "code": "FB32.2Z", "title": "Ischaemic infarction of muscle, unspecified" }, { "code": "FB56.2", "title": "Myalgia" } ]
=== ICD-11 CODES FOUND === [2F9Z] Neoplasms of unknown behaviour of unspecified site Also known as: Neoplasms of unknown behaviour of unspecified site | neoplasia | neoplasm growth NOS | tumour of unspecified site | tumourlet of unspecified site [ME61] Subcutaneous swelling, mass or lump of uncertain or unspecified nature Definition: One or more localised subcutaneous soft tissue masses of undetermined or unspecified nature Also known as: Subcutaneous swelling, mass or lump of uncertain or unspecified nature | localised swelling, mass or lump of skin and subcutaneous tissue | localised subcutaneous nodules | subcutaneous nodules | superficial subcutaneous nodules Excludes: localized adiposity | mass and lump: breast | enlarged lymph nodes [2E6Z] Carcinoma in situ of unspecified site Also known as: Carcinoma in situ of unspecified site | carcinoma in situ of unspecified site | carcinoma in situ NOS | carcinoma in situ | in situ neoplasm [2F91.1] Neoplasms of unknown behaviour of trachea, bronchus or lung Also known as: Neoplasms of unknown behaviour of trachea, bronchus or lung | trachea, bronchus or lung tumour NOS | Intravascular bronchial alveolar tumour of unspecified site | Bronchial adenoma of unknown behaviour of unspecified site | Intravascular bronchial alveolar tumour unknown behaviour of unspecified site [2F92] Neoplasms of unknown behaviour of skin Also known as: Neoplasms of unknown behaviour of skin | skin tumour NOS [FB3Z] Disorders of muscles, unspecified Also known as: Disorders of muscles, unspecified | disorder of muscle, unspecified | muscle disease | muscular disease | muscular disorder [FB32.Y] Other specified disorders of muscles Also known as: Other specified disorders of muscles | Muscle wasting or atrophy, not elsewhere classified | muscle wasting | muscle wasting disorder | Sarcopenia [8C70.Z] Muscular dystrophy, unspecified Also known as: Muscular dystrophy, unspecified | Muscular dystrophy | Gower's muscular dystrophy | progressive musclular dystrophy | pseudohypertrophic atrophy [FB32.2Z] Ischaemic infarction of muscle, unspecified Also known as: Ischaemic infarction of muscle, unspecified | Ischaemic infarction of muscle | muscle infarction [FB56.2] Myalgia Definition: This is a disorder characterised by pain in a muscle or group of muscles. Also known as: Myalgia | muscle ache | muscle soreness | muscular pain | myalgic Excludes: Chronic primary musculoskeletal pain | Chronic secondary musculoskeletal pain === GRAPH WALKS === --- Walk 1 --- [2F9Z] Neoplasms of unknown behaviour of unspecified site --PARENT--> [?] Neoplasms of unknown behaviour, except of lymphoid, haematopoietic, central nervous system or related tissues --CHILD--> [2F90] Neoplasms of unknown behaviour of oral cavity or digestive organs --- Walk 2 --- [2F9Z] Neoplasms of unknown behaviour of unspecified site --PARENT--> [?] Neoplasms of unknown behaviour, except of lymphoid, haematopoietic, central nervous system or related tissues --CHILD--> [2F91] Neoplasms of unknown behaviour of middle ear, respiratory or intrathoracic organs --- Walk 3 --- [ME61] Subcutaneous swelling, mass or lump of uncertain or unspecified nature Def: One or more localised subcutaneous soft tissue masses of undetermined or unspecified nature... --EXCLUDES--> [?] Breast lump or mass female --PARENT--> [?] Symptoms, signs or clinical findings involving the female genital system --- Walk 4 --- [ME61] Subcutaneous swelling, mass or lump of uncertain or unspecified nature Def: One or more localised subcutaneous soft tissue masses of undetermined or unspecified nature... --EXCLUDES--> [?] Breast lump or mass female --PARENT--> [?] Symptoms, signs or clinical findings involving the female genital system --- Walk 5 --- [2E6Z] Carcinoma in situ of unspecified site --PARENT--> [?] In situ neoplasms, except of lymphoid, haematopoietic, central nervous system or related tissues --CHILD--> [2E60] Carcinoma in situ of oral cavity, oesophagus or stomach --- Walk 6 --- [2E6Z] Carcinoma in situ of unspecified site --PARENT--> [?] In situ neoplasms, except of lymphoid, haematopoietic, central nervous system or related tissues --CHILD--> [2E60] Carcinoma in situ of oral cavity, oesophagus or stomach
[ "[2F9Z] Neoplasms of unknown behaviour of unspecified site\n --PARENT--> [?] Neoplasms of unknown behaviour, except of lymphoid, haematopoietic, central nervous system or related tissues\n --CHILD--> [2F90] Neoplasms of unknown behaviour of oral cavity or digestive organs", "[2F9Z] Neoplasms of unknown behaviour of unspecified site\n --PARENT--> [?] Neoplasms of unknown behaviour, except of lymphoid, haematopoietic, central nervous system or related tissues\n --CHILD--> [2F91] Neoplasms of unknown behaviour of middle ear, respiratory or intrathoracic organs", "[ME61] Subcutaneous swelling, mass or lump of uncertain or unspecified nature\n Def: One or more localised subcutaneous soft tissue masses of undetermined or unspecified nature...\n --EXCLUDES--> [?] Breast lump or mass female\n --PARENT--> [?] Symptoms, signs or clinical findings involving the female genital system", "[ME61] Subcutaneous swelling, mass or lump of uncertain or unspecified nature\n Def: One or more localised subcutaneous soft tissue masses of undetermined or unspecified nature...\n --EXCLUDES--> [?] Breast lump or mass female\n --PARENT--> [?] Symptoms, signs or clinical findings involving the female genital system", "[2E6Z] Carcinoma in situ of unspecified site\n --PARENT--> [?] In situ neoplasms, except of lymphoid, haematopoietic, central nervous system or related tissues\n --CHILD--> [2E60] Carcinoma in situ of oral cavity, oesophagus or stomach", "[2E6Z] Carcinoma in situ of unspecified site\n --PARENT--> [?] In situ neoplasms, except of lymphoid, haematopoietic, central nervous system or related tissues\n --CHILD--> [2E60] Carcinoma in situ of oral cavity, oesophagus or stomach" ]
2F9Z
Neoplasms of unknown behaviour of unspecified site
[ { "from_icd11": "2F9Z", "icd10_code": "D487", "icd10_title": "Neoplasm of uncertain behavior of other specified sites" }, { "from_icd11": "2F9Z", "icd10_code": "D482", "icd10_title": "Neoplasm of uncertain behavior of peripheral nerves and autonomic nervous system" }, { "from_icd11": "2F9Z", "icd10_code": "D37-D48", "icd10_title": "" }, { "from_icd11": "2F9Z", "icd10_code": "D377", "icd10_title": "" }, { "from_icd11": "2F9Z", "icd10_code": "D48", "icd10_title": "Neoplasm of uncertain behavior of other and unspecified sites" }, { "from_icd11": "2F9Z", "icd10_code": "D489", "icd10_title": "Neoplasm of uncertain behavior, unspecified" }, { "from_icd11": "ME61", "icd10_code": "R2240", "icd10_title": "Localized swelling, mass and lump, unspecified lower limb" }, { "from_icd11": "ME61", "icd10_code": "R2232", "icd10_title": "Localized swelling, mass and lump, left upper limb" }, { "from_icd11": "ME61", "icd10_code": "R2242", "icd10_title": "Localized swelling, mass and lump, left lower limb" }, { "from_icd11": "ME61", "icd10_code": "R2231", "icd10_title": "Localized swelling, mass and lump, right upper limb" }, { "from_icd11": "ME61", "icd10_code": "R2241", "icd10_title": "Localized swelling, mass and lump, right lower limb" }, { "from_icd11": "ME61", "icd10_code": "R2233", "icd10_title": "Localized swelling, mass and lump, upper limb, bilateral" }, { "from_icd11": "ME61", "icd10_code": "R2243", "icd10_title": "Localized swelling, mass and lump, lower limb, bilateral" }, { "from_icd11": "ME61", "icd10_code": "R2230", "icd10_title": "Localized swelling, mass and lump, unspecified upper limb" }, { "from_icd11": "ME61", "icd10_code": "R220", "icd10_title": "Localized swelling, mass and lump, head" } ]
D487
Neoplasm of uncertain behavior of other specified sites
First-degree relatives underwent genetic counselling. Proband’s mother carried the variant. She was offered clinical assessment, including biochemical and imaging tests of the pancreas, the pituitary, and the adrenal glands. Lab tests showed hypercalcemia (2.97 mmol/L) and elevated PTH . US of the neck revealed a hypoechoic nodule (0.5 × 0.3 cm) posterior to the left thyroid lobe and scintigraphy using TcMIBI showed an increased tracer uptake in the same location, so she was diagnosed with PHPT. Abdominal US confirmed the presence of renal lithiasis. Due to densitometric osteoporosis (lumbar spine 0.637 g/cm 2 and T score − 4.69 SD; femoral neck 0.593 g/cm 2 and T score − 3.23 SD), alendronate was prescribed. We performed unilateral neck exploration with the removal of a single parathyroid adenoma. PTH levels declined to normal after excision. CT scan of the chest and abdomen did not show abnormalities. Regarding pituitary hormones, lab test showed a low morning serum cortisol level (5.04 µg/dL; RV 6.02–18.4) with low adrenocorticotropin hormone level (4.2 pg/mL; RV 7.2–63.3), pattern suggesting secondary adrenal insufficiency. We performed a 250 µg cosyntropin stimulation test, which showed normal post-stimulation cortisol levels: (1) 30 min − 26.9 µg/dL and (2) 60 min 31.9 µg/dL (RV > 14 µg/dL). No other lab pituitary hormone alterations or radiological abnormalities of the gland were detected.
4.078125
0.947754
sec[3]/sec[3]/p[0]
en
0.999997
36334246
https://doi.org/10.1007/s40618-022-01948-7
[ "pituitary", "neck", "adrenal", "score", "abnormalities", "cortisol", "hormone", "stimulation", "degree", "relatives" ]
[ { "code": "5A61", "title": "Hypofunction or certain other specified disorders of pituitary gland" }, { "code": "5A61.0", "title": "Hypopituitarism" }, { "code": "5A61.Y", "title": "Other specified hypofunction or disorders of pituitary gland" }, { "code": "5D43", "title": "Postprocedural hypopituitarism" }, { "code": "2F9A&XA8J35", "title": "Neoplasms of unknown behaviour of pituitary gland" }, { "code": "ME86.C", "title": "Symptom or complaint of the neck" }, { "code": "LA6Z", "title": "Structural developmental anomalies of the neck, unspecified" }, { "code": "ME84.0", "title": "Cervical spine pain" }, { "code": "FA71", "title": "Torticollis" }, { "code": "NA23.4Y", "title": "Other specified strain or sprain of cervical spine" } ]
=== ICD-11 CODES FOUND === [5A61] Hypofunction or certain other specified disorders of pituitary gland Definition: Clinical status with disordered function of the pituitary gland without excessive pituitary hormone production, which is caused by a variety of diseases Also known as: Hypofunction or certain other specified disorders of pituitary gland | disorder of pituitary gland | pituitary disease | pituitary gland disease | pituitary glandular disease Excludes: Postprocedural hypopituitarism | Craniopharyngioma [5A61.0] Hypopituitarism Definition: A disorder manifesting a deficiency or decrease of one or more pituitary hormones, which is caused by a variety of diseases such as tumour, trauma/surgery, irradiation, inflammation and haemorrhage/infarction. Also known as: Hypopituitarism | subpituitarism | hypophyseal dystrophy | hypohypophysism | anterior pituitary insufficiency (in part) Includes: pituitary cachexia | pituitary short stature [5A61.Y] Other specified hypofunction or disorders of pituitary gland Also known as: Other specified hypofunction or disorders of pituitary gland | Prolactin deficiency | Isolated prolactin deficiency | Hypothalamic dysfunction, not elsewhere classified | dyspituitarism [5D43] Postprocedural hypopituitarism Definition: This is the postprocedural decreased (hypo) secretion of one or more of the eight hormones normally produced by the pituitary gland at the base of the brain. If there is decreased secretion of most pituitary hormones, the term panhypopituitarism (pan meaning "all") is used. Also known as: Postprocedural hypopituitarism | iatrogenic pituitary disorder | acquired pituitary gland absence | acquired pituitary glandular absence | iatrogenic postprocedural pituitary disorder [ME86.C] Symptom or complaint of the neck Also known as: Symptom or complaint of the neck | Neck syndrome Excludes: Chronic primary musculoskeletal pain | Chronic secondary musculoskeletal pain [LA6Z] Structural developmental anomalies of the neck, unspecified Also known as: Structural developmental anomalies of the neck, unspecified | Malformations of the neck [ME84.0] Cervical spine pain Definition: This is a condition which is usually characterised by pain or discomfort in the neck region and can be caused by numerous spinal problems. It may be a feature of virtually every disorder and disease that occurs above the shoulder blades. Also known as: Cervical spine pain | cervical pain | neck ache | nonspecific pain in the neck region | cervicalgia Includes: cervicalgia Excludes: cervical disc degeneration | Chronic primary cervical pain | Chronic secondary musculoskeletal pain [FA71] Torticollis Also known as: Torticollis | contracture of neck | wry neck | wry neck/torticollis | Intermittent torticollis Excludes: Cervical dystonia | Congenital torticollis | current injury - see injury of spine by body region [NA23.4Y] Other specified strain or sprain of cervical spine Also known as: Other specified strain or sprain of cervical spine | Strain of cervical spine | cervical strain | Strain of cervical anterior longitudinal ligament | Sprain of cervical spine === GRAPH WALKS === --- Walk 1 --- [5A61] Hypofunction or certain other specified disorders of pituitary gland Def: Clinical status with disordered function of the pituitary gland without excessive pituitary hormone production, which is caused by a variety of diseases... --RELATED_TO--> [?] Non-secreting pituitary adenoma --PARENT--> [?] Benign neoplasm of endocrine glands --- Walk 2 --- [5A61] Hypofunction or certain other specified disorders of pituitary gland Def: Clinical status with disordered function of the pituitary gland without excessive pituitary hormone production, which is caused by a variety of diseases... --CHILD--> [5A61.2] Gonadotropin deficiency Def: Deficiency of Luteinizing Hormone (LH), Follicle Stimulating Hormone (FSH) resulting in hypogonadism (male and female). Includes deficiency of Gonadotropin Releasing Hormone (GnRH, LHRH).... --EXCLUDES--> [?] Testicular hypofunction Def: In pre-puberty, a disorder characterised by atrophied testes and sterility, abnormal height and absence of secondary sex characteristics. In post-puberty, a disorder characterised by depressed sexual ... --- Walk 3 --- [5A61.0] Hypopituitarism Def: A disorder manifesting a deficiency or decrease of one or more pituitary hormones, which is caused by a variety of diseases such as tumour, trauma/surgery, irradiation, inflammation and haemorrhage/in... --PARENT--> [5A61] Hypofunction or certain other specified disorders of pituitary gland Def: Clinical status with disordered function of the pituitary gland without excessive pituitary hormone production, which is caused by a variety of diseases... --CHILD--> [5A61.0] Hypopituitarism Def: A disorder manifesting a deficiency or decrease of one or more pituitary hormones, which is caused by a variety of diseases such as tumour, trauma/surgery, irradiation, inflammation and haemorrhage/in... --- Walk 4 --- [5A61.0] Hypopituitarism Def: A disorder manifesting a deficiency or decrease of one or more pituitary hormones, which is caused by a variety of diseases such as tumour, trauma/surgery, irradiation, inflammation and haemorrhage/in... --RELATED_TO--> [?] Argonz-del Castillo Syndrome --PARENT--> [?] Functional hyperprolactinoma Def: Increased blood level of prolactin caused by non-tumourous mechanisms such as disruption of pituitary stalk, severe hypothyroidism, or administration of dopamine receptor antagonists.... --- Walk 5 --- [5A61.Y] Other specified hypofunction or disorders of pituitary gland --PARENT--> [5A61] Hypofunction or certain other specified disorders of pituitary gland Def: Clinical status with disordered function of the pituitary gland without excessive pituitary hormone production, which is caused by a variety of diseases... --CHILD--> [5A61.0] Hypopituitarism Def: A disorder manifesting a deficiency or decrease of one or more pituitary hormones, which is caused by a variety of diseases such as tumour, trauma/surgery, irradiation, inflammation and haemorrhage/in... --- Walk 6 --- [5A61.Y] Other specified hypofunction or disorders of pituitary gland --PARENT--> [5A61] Hypofunction or certain other specified disorders of pituitary gland Def: Clinical status with disordered function of the pituitary gland without excessive pituitary hormone production, which is caused by a variety of diseases... --EXCLUDES--> [?] Primary neoplasms of brain
[ "[5A61] Hypofunction or certain other specified disorders of pituitary gland\n Def: Clinical status with disordered function of the pituitary gland without excessive pituitary hormone production, which is caused by a variety of diseases...\n --RELATED_TO--> [?] Non-secreting pituitary adenoma\n --PARENT--> [?] Benign neoplasm of endocrine glands", "[5A61] Hypofunction or certain other specified disorders of pituitary gland\n Def: Clinical status with disordered function of the pituitary gland without excessive pituitary hormone production, which is caused by a variety of diseases...\n --CHILD--> [5A61.2] Gonadotropin deficiency\n Def: Deficiency of Luteinizing Hormone (LH), Follicle Stimulating Hormone (FSH) resulting in hypogonadism (male and female). Includes deficiency of Gonadotropin Releasing Hormone (GnRH, LHRH)....\n --EXCLUDES--> [?] Testicular hypofunction\n Def: In pre-puberty, a disorder characterised by atrophied testes and sterility, abnormal height and absence of secondary sex characteristics. In post-puberty, a disorder characterised by depressed sexual ...", "[5A61.0] Hypopituitarism\n Def: A disorder manifesting a deficiency or decrease of one or more pituitary hormones, which is caused by a variety of diseases such as tumour, trauma/surgery, irradiation, inflammation and haemorrhage/in...\n --PARENT--> [5A61] Hypofunction or certain other specified disorders of pituitary gland\n Def: Clinical status with disordered function of the pituitary gland without excessive pituitary hormone production, which is caused by a variety of diseases...\n --CHILD--> [5A61.0] Hypopituitarism\n Def: A disorder manifesting a deficiency or decrease of one or more pituitary hormones, which is caused by a variety of diseases such as tumour, trauma/surgery, irradiation, inflammation and haemorrhage/in...", "[5A61.0] Hypopituitarism\n Def: A disorder manifesting a deficiency or decrease of one or more pituitary hormones, which is caused by a variety of diseases such as tumour, trauma/surgery, irradiation, inflammation and haemorrhage/in...\n --RELATED_TO--> [?] Argonz-del Castillo Syndrome\n --PARENT--> [?] Functional hyperprolactinoma\n Def: Increased blood level of prolactin caused by non-tumourous mechanisms such as disruption of pituitary stalk, severe hypothyroidism, or administration of dopamine receptor antagonists....", "[5A61.Y] Other specified hypofunction or disorders of pituitary gland\n --PARENT--> [5A61] Hypofunction or certain other specified disorders of pituitary gland\n Def: Clinical status with disordered function of the pituitary gland without excessive pituitary hormone production, which is caused by a variety of diseases...\n --CHILD--> [5A61.0] Hypopituitarism\n Def: A disorder manifesting a deficiency or decrease of one or more pituitary hormones, which is caused by a variety of diseases such as tumour, trauma/surgery, irradiation, inflammation and haemorrhage/in...", "[5A61.Y] Other specified hypofunction or disorders of pituitary gland\n --PARENT--> [5A61] Hypofunction or certain other specified disorders of pituitary gland\n Def: Clinical status with disordered function of the pituitary gland without excessive pituitary hormone production, which is caused by a variety of diseases...\n --EXCLUDES--> [?] Primary neoplasms of brain" ]
5A61
Hypofunction or certain other specified disorders of pituitary gland
[ { "from_icd11": "5A61", "icd10_code": "E233", "icd10_title": "Hypothalamic dysfunction, not elsewhere classified" }, { "from_icd11": "5A61", "icd10_code": "E23", "icd10_title": "Hypofunction and other disorders of the pituitary gland" }, { "from_icd11": "5A61.0", "icd10_code": "E230", "icd10_title": "Hypopituitarism" }, { "from_icd11": "5A61.0", "icd10_code": "Q044", "icd10_title": "Septo-optic dysplasia of brain" }, { "from_icd11": "5A61.0", "icd10_code": "E231", "icd10_title": "Drug-induced hypopituitarism" }, { "from_icd11": "5D43", "icd10_code": "E893", "icd10_title": "Postprocedural hypopituitarism" }, { "from_icd11": "2F9A&XA8J35", "icd10_code": "D443", "icd10_title": "Neoplasm of uncertain behavior of pituitary gland" }, { "from_icd11": "LA6Z", "icd10_code": "Q680", "icd10_title": "Congenital deformity of sternocleidomastoid muscle" }, { "from_icd11": "LA6Z", "icd10_code": "Q180", "icd10_title": "Sinus, fistula and cyst of branchial cleft" }, { "from_icd11": "LA6Z", "icd10_code": "Q188", "icd10_title": "Other specified congenital malformations of face and neck" }, { "from_icd11": "LA6Z", "icd10_code": "Q10-Q18", "icd10_title": "" }, { "from_icd11": "LA6Z", "icd10_code": "Q182", "icd10_title": "Other branchial cleft malformations" }, { "from_icd11": "ME84.0", "icd10_code": "M542", "icd10_title": "Cervicalgia" }, { "from_icd11": "ME84.0", "icd10_code": "M530", "icd10_title": "Cervicocranial syndrome" }, { "from_icd11": "ME84.0", "icd10_code": "M531", "icd10_title": "Cervicobrachial syndrome" } ]
E233
Hypothalamic dysfunction, not elsewhere classified
Fewer than 15 cases of schwannoma recurrence after surgical excision have been reported in the literature. While our patient recovered from the operation without complications, his initial workup at our dermatology clinic was complex. His biopsy site from where we performed a punch biopsy had an exaggerated injury response, or pathergy . Pathergy is characterized by a state of altered tissue reactivity in response to trauma and is often used as a diagnostic test of Behçet's syndrome with a needle prick to look for evidence of this phenomenon . Pathergy can also be seen in other inflammatory conditions such as Crohn's disease, pyoderma gangrenosum, and Sweet's syndrome . After the shave excision of the patient’s persistent schwannoma, the site became markedly ulcerated and developed protuberant beefy red granulation tissue, once again felt to be consistent with pathergy. To our knowledge, there have been no cases reported in the literature where a patient with a schwannoma has experienced pathergy following a biopsy procedure for tissue diagnosis. We believe the pathogenesis of pathergy in our patient could be related to disturbance of the localized tissue while performing a biopsy. Physicians should be aware of these sequelae so that they may properly educate their patients to anticipate them as possible negative outcomes secondary to biopsy, and subsequently recognize and treat the complication.
4.117188
0.811523
sec[2]/p[2]
en
0.999998
PMC9587802
https://doi.org/10.7759/cureus.29463
[ "pathergy", "biopsy", "tissue", "schwannoma", "cases", "excision", "literature", "while", "site", "response" ]
[ { "code": "JA85.Y", "title": "Maternal care for other specified fetal abnormality or damage" }, { "code": "KD39.3", "title": "Fetus or newborn affected by complications of fetal surgery" }, { "code": "PK81.5", "title": "Biopsy procedure, not elsewhere classified, associated with injury or harm in therapeutic use" }, { "code": "PK81.4", "title": "Bone marrow aspiration or biopsy associated with injury or harm in therapeutic use" }, { "code": "PK98.0", "title": "Radiological devices associated with injury or harm, diagnostic or monitoring devices" }, { "code": "FB6Z", "title": "Soft tissue disorders, unspecified" }, { "code": "MC85", "title": "Gangrene" }, { "code": "FB56.6", "title": "Other specified soft tissue disorders" }, { "code": "GB61.Z", "title": "Chronic kidney disease, stage unspecified" }, { "code": "4A43.3", "title": "Mixed connective tissue disease" } ]
=== ICD-11 CODES FOUND === [JA85.Y] Maternal care for other specified fetal abnormality or damage Also known as: Maternal care for other specified fetal abnormality or damage | Maternal care for damage to fetus from alcohol | suspected damage to fetus from maternal alcohol addiction affecting management of mother | pregnancy management affected by fetal damage from maternal alcohol addiction | maternal care for known or suspected damage to fetus from alcohol [KD39.3] Fetus or newborn affected by complications of fetal surgery Definition: A condition in the fetus due to an unfavourable evolution of a condition (complication) associated with a surgical health intervention applied to the fetus. Also known as: Fetus or newborn affected by complications of fetal surgery | Adverse outcome following fetal skin biopsy [PK81.5] Biopsy procedure, not elsewhere classified, associated with injury or harm in therapeutic use Also known as: Biopsy procedure, not elsewhere classified, associated with injury or harm in therapeutic use | complication during or following biopsy procedure, other than bone marrow Excludes: Bone marrow aspiration or biopsy associated with injury or harm in therapeutic use | Circumstances associated with a surgical or other medical procedure influencing the episode of care, without injury or harm [PK81.4] Bone marrow aspiration or biopsy associated with injury or harm in therapeutic use Also known as: Bone marrow aspiration or biopsy associated with injury or harm in therapeutic use | complication during or following bone marrow aspiration or biopsy Excludes: Circumstances associated with a surgical or other medical procedure influencing the episode of care, without injury or harm [PK98.0] Radiological devices associated with injury or harm, diagnostic or monitoring devices Also known as: Radiological devices associated with injury or harm, diagnostic or monitoring devices | Radiological devices associated with adverse incidents, malfunction of radiological apparatus | Radiological devices associated with adverse incidents, CT scanner or MRI causing physical injury | Radiological devices associated with adverse incidents, needles used in radiologically-guided biopsies Excludes: Circumstances associated with a surgical or other medical device influencing the episode of care without injury or harm [FB6Z] Soft tissue disorders, unspecified Also known as: Soft tissue disorders, unspecified | disease of soft tissue NOS | unspecified soft tissue disorder, site unspecified | disorder of soft tissue | disorder of soft tissue NOS [MC85] Gangrene Definition: Gangrene, not elsewhere classified is the death of tissues in the body which happens when a part of the body loses its blood supply. Also known as: Gangrene | gangrene NOS | dry gangrene | wet gangrene | ulcerative gangrene Excludes: Pyoderma gangrenosum | Gas gangrene | Polymicrobial necrotising fasciitis [FB56.6] Other specified soft tissue disorders Also known as: Other specified soft tissue disorders | Fat necrosis | fatty necrosis | Profichet's disease | Sloughing of fascia [GB61.Z] Chronic kidney disease, stage unspecified Also known as: Chronic kidney disease, stage unspecified | Chronic kidney disease | chronic renal failure | chronic kidney failure | chronic renal disease [4A43.3] Mixed connective tissue disease Definition: Mixed connective tissue disease is an overlapping syndrome combining features of systemic lupus erythematosus, systemic sclerosis, and polymyositis with the presence of autoantibodies to U1-ribonucleoprotein. Raynaud’s phenomenon is seen in nearly all patients and pulmonary arterial hypertension is the most common cause of death in MCTD patients. Also known as: Mixed connective tissue disease | Sharp syndrome | MCTD - [mixed connective tissue disease] | Paediatric-onset mixed connective tissue disease | Paediatric-onset Sharp syndrome === GRAPH WALKS === --- Walk 1 --- [JA85.Y] Maternal care for other specified fetal abnormality or damage --PARENT--> [JA85] Maternal care for fetal abnormality or damage Def: A condition characterised by the provision of health interventions to the mother due to some abnormality or damage that is either suspected or known to be present in the fetus.... --CHILD--> [JA85.2] Maternal care for hereditary disease in fetus --- Walk 2 --- [JA85.Y] Maternal care for other specified fetal abnormality or damage --PARENT--> [JA85] Maternal care for fetal abnormality or damage Def: A condition characterised by the provision of health interventions to the mother due to some abnormality or damage that is either suspected or known to be present in the fetus.... --EXCLUDES--> [?] Maternal care for disproportion Def: A condition characterised by the provision of health interventions to the mother due to the situation in which the head or body of the fetus is too large to fit through the pelvis of the mother.... --- Walk 3 --- [KD39.3] Fetus or newborn affected by complications of fetal surgery Def: A condition in the fetus due to an unfavourable evolution of a condition (complication) associated with a surgical health intervention applied to the fetus.... --PARENT--> [KD39] Complications of intrauterine procedures, not elsewhere classified Def: A group of conditions characterised as an unfavourable evolution of a condition (complication) due to a health intervention applied inside of the uterus.... --EXCLUDES--> [?] Fetus or newborn affected by other forms of placental separation Def: A group of conditions characterised by findings in the fetus or newborn due to when the placental separates from the uterus of the mother or when the fetus of newborn is suspected to be affected by pl... --- Walk 4 --- [KD39.3] Fetus or newborn affected by complications of fetal surgery Def: A condition in the fetus due to an unfavourable evolution of a condition (complication) associated with a surgical health intervention applied to the fetus.... --PARENT--> [KD39] Complications of intrauterine procedures, not elsewhere classified Def: A group of conditions characterised as an unfavourable evolution of a condition (complication) due to a health intervention applied inside of the uterus.... --EXCLUDES--> [?] Fetus or newborn affected by other forms of placental separation Def: A group of conditions characterised by findings in the fetus or newborn due to when the placental separates from the uterus of the mother or when the fetus of newborn is suspected to be affected by pl... --- Walk 5 --- [PK81.5] Biopsy procedure, not elsewhere classified, associated with injury or harm in therapeutic use --EXCLUDES--> [?] Circumstances associated with a surgical or other medical procedure influencing the episode of care, without injury or harm --EXCLUDES--> [?] Mode of injury or harm associated with a surgical or other medical procedure --- Walk 6 --- [PK81.5] Biopsy procedure, not elsewhere classified, associated with injury or harm in therapeutic use --EXCLUDES--> [?] Bone marrow aspiration or biopsy associated with injury or harm in therapeutic use --PARENT--> [?] Certain medical procedures associated with injury or harm in therapeutic use
[ "[JA85.Y] Maternal care for other specified fetal abnormality or damage\n --PARENT--> [JA85] Maternal care for fetal abnormality or damage\n Def: A condition characterised by the provision of health interventions to the mother due to some abnormality or damage that is either suspected or known to be present in the fetus....\n --CHILD--> [JA85.2] Maternal care for hereditary disease in fetus", "[JA85.Y] Maternal care for other specified fetal abnormality or damage\n --PARENT--> [JA85] Maternal care for fetal abnormality or damage\n Def: A condition characterised by the provision of health interventions to the mother due to some abnormality or damage that is either suspected or known to be present in the fetus....\n --EXCLUDES--> [?] Maternal care for disproportion\n Def: A condition characterised by the provision of health interventions to the mother due to the situation in which the head or body of the fetus is too large to fit through the pelvis of the mother....", "[KD39.3] Fetus or newborn affected by complications of fetal surgery\n Def: A condition in the fetus due to an unfavourable evolution of a condition (complication) associated with a surgical health intervention applied to the fetus....\n --PARENT--> [KD39] Complications of intrauterine procedures, not elsewhere classified\n Def: A group of conditions characterised as an unfavourable evolution of a condition (complication) due to a health intervention applied inside of the uterus....\n --EXCLUDES--> [?] Fetus or newborn affected by other forms of placental separation\n Def: A group of conditions characterised by findings in the fetus or newborn due to when the placental separates from the uterus of the mother or when the fetus of newborn is suspected to be affected by pl...", "[KD39.3] Fetus or newborn affected by complications of fetal surgery\n Def: A condition in the fetus due to an unfavourable evolution of a condition (complication) associated with a surgical health intervention applied to the fetus....\n --PARENT--> [KD39] Complications of intrauterine procedures, not elsewhere classified\n Def: A group of conditions characterised as an unfavourable evolution of a condition (complication) due to a health intervention applied inside of the uterus....\n --EXCLUDES--> [?] Fetus or newborn affected by other forms of placental separation\n Def: A group of conditions characterised by findings in the fetus or newborn due to when the placental separates from the uterus of the mother or when the fetus of newborn is suspected to be affected by pl...", "[PK81.5] Biopsy procedure, not elsewhere classified, associated with injury or harm in therapeutic use\n --EXCLUDES--> [?] Circumstances associated with a surgical or other medical procedure influencing the episode of care, without injury or harm\n --EXCLUDES--> [?] Mode of injury or harm associated with a surgical or other medical procedure", "[PK81.5] Biopsy procedure, not elsewhere classified, associated with injury or harm in therapeutic use\n --EXCLUDES--> [?] Bone marrow aspiration or biopsy associated with injury or harm in therapeutic use\n --PARENT--> [?] Certain medical procedures associated with injury or harm in therapeutic use" ]
JA85.Y
Maternal care for other specified fetal abnormality or damage
[ { "from_icd11": "JA85.Y", "icd10_code": "O358XX0 ", "icd10_title": "" }, { "from_icd11": "JA85.Y", "icd10_code": "O358XX1 ", "icd10_title": "" }, { "from_icd11": "PK98.0", "icd10_code": "Y780", "icd10_title": "Diagnostic and monitoring radiological devices associated with adverse incidents" }, { "from_icd11": "FB6Z", "icd10_code": "M60-M79", "icd10_title": "" }, { "from_icd11": "MC85", "icd10_code": "R02", "icd10_title": "" }, { "from_icd11": "MC85", "icd10_code": "I96", "icd10_title": "Gangrene, not elsewhere classified" }, { "from_icd11": "FB56.6", "icd10_code": "M7981", "icd10_title": "Nontraumatic hematoma of soft tissue" }, { "from_icd11": "FB56.6", "icd10_code": "M7989", "icd10_title": "Other specified soft tissue disorders" }, { "from_icd11": "FB56.6", "icd10_code": "M798", "icd10_title": "Other specified soft tissue disorders" }, { "from_icd11": "GB61.Z", "icd10_code": "N183", "icd10_title": "Chronic kidney disease, stage 3 (moderate)" }, { "from_icd11": "GB61.Z", "icd10_code": "N189", "icd10_title": "Chronic kidney disease, unspecified" }, { "from_icd11": "GB61.Z", "icd10_code": "N250", "icd10_title": "Renal osteodystrophy" }, { "from_icd11": "GB61.Z", "icd10_code": "N18", "icd10_title": "Chronic kidney disease (CKD)" }, { "from_icd11": "4A43.3", "icd10_code": "M351", "icd10_title": "Other overlap syndromes" }, { "from_icd11": "4A43.3", "icd10_code": "M35", "icd10_title": "Other systemic involvement of connective tissue" } ]
O358XX0
On admission, the patient’s vital signs were stable, with a blood pressure of 130/80 mm Hg, pulse rate of 82 beats/minute, and body temperature of 36.5 °C. Physical examination revealed a poor performance status and conjunctival pallor. The abdomen was soft and undistended. Other physical examinations were unremarkable. The results of a complete blood count test revealed a hemoglobin of 6.4 g/dL, hematocrit of 19%, mean corpuscular volume of 108.2 fL, mean corpuscular hemoglobin of 36.3 pg, and mean corpuscular hemoglobin concentration of 33.6%. The results of the blood chemistry tests were within normal reference limits: total bilirubin of 0.6 mg/dL (reference range 0.2–1.2 mg/dL), aspartate aminotransferase of 27 IU/L (reference range 8–40 IU/L), alanine aminotransferase of 9 IU/L (reference range 5–41 IU/L), alkaline phosphatase of 100 IU/L (reference rage 40–130 IU/L), serum amylase of 77 IU/L (reference range 41–134 IU/L), and serum lipase of 39 IU/L (reference range 13–60 IU/L). In the emergency room, initial upper and lower gastrointestinal endoscopies did not reveal the source of bleeding. The pre-contrast phase CT scans showed severe fatty changes in the liver, gallbladder stones, and multiple calcifications at the pancreatic tail . Arterial phase CT scans showed peripancreatic inflammation at the tail of the pancreas and a tortuous splenic artery , without a definite source of bleeding.
3.910156
0.974121
sec[1]/p[1]
en
0.999997
PMC9666211
https://doi.org/10.1097/MD.0000000000031561
[ "reference", "range", "blood", "hemoglobin", "mean", "corpuscular", "physical", "aminotransferase", "serum", "source" ]
[ { "code": "6B22.Z", "title": "Olfactory reference disorder, unspecified" }, { "code": "MB26.03", "title": "Delusion of reference" }, { "code": "6B22.1", "title": "Olfactory reference disorder with poor to absent insight" }, { "code": "4B00.0Z", "title": "Neutropaenia, unspecified" }, { "code": "3B63.1Z", "title": "Acquired thrombocytosis, unspecified" }, { "code": "QA00.6Y", "title": "Other specified examination of eyes or vision" }, { "code": "MA14.1C", "title": "Raised antibody titre" }, { "code": "BD11.1", "title": "Left ventricular failure with mid range ejection fraction" }, { "code": "3C0Z", "title": "Diseases of the blood or blood-forming organs, unspecified" }, { "code": "MF50.4Z", "title": "Haematuria, unspecified" } ]
=== ICD-11 CODES FOUND === [6B22.Z] Olfactory reference disorder, unspecified Also known as: Olfactory reference disorder, unspecified | Olfactory reference disorder | Delusions of malodour [MB26.03] Delusion of reference Definition: A delusion that events, objects, or other people in the person's immediate environment have a particular and unusual personal significance, usually of a negative or pejorative nature. Also known as: Delusion of reference [6B22.1] Olfactory reference disorder with poor to absent insight Definition: All definitional requirements of olfactory reference disorder are met. Most or all of the time, the individual is convinced that the disorder-specific beliefs are true and cannot accept an alternative explanation for their experience. The lack of insight exhibited by the individual does not vary markedly as a function of anxiety level. Also known as: Olfactory reference disorder with poor to absent insight [4B00.0Z] Neutropaenia, unspecified Also known as: Neutropaenia, unspecified | Neutropenia | Disorders with decreased neutrophil counts | neutropaenic disorder | neutrophil count below reference range [3B63.1Z] Acquired thrombocytosis, unspecified Also known as: Acquired thrombocytosis, unspecified | Acquired thrombocytosis | Idiopathic haemorrhagic thrombocythaemia | Essential thrombocythaemia | primary haemorrhagic thrombocythaemia [QA00.6Y] Other specified examination of eyes or vision Also known as: Other specified examination of eyes or vision | No Impairment of Contrast vision | Normal colour vision | No Impairment of Dark adaptation | No diplopia [MA14.1C] Raised antibody titre Also known as: Raised antibody titre | antibody titre above reference range | high antibody titre | increased antibody titre Excludes: isoimmunization, in pregnancy affecting fetus or newborn [BD11.1] Left ventricular failure with mid range ejection fraction Also known as: Left ventricular failure with mid range ejection fraction | HFmEF - [heart failure with mid range ejection fraction] | Left ventricular failure with mid range ejection fraction due to cardiomyopathy | Left ventricular failure with mid range ejection fraction due to coronary artery disease | Left ventricular failure with mid range ejection fraction due to myocarditis [3C0Z] Diseases of the blood or blood-forming organs, unspecified Also known as: Diseases of the blood or blood-forming organs, unspecified | Blood, lymph or spleen disease | blood condition NOS | blood disorder NOS | bone marrow disease NOS [MF50.4Z] Haematuria, unspecified Also known as: Haematuria, unspecified | Haematuria | blood in urine | urinary blood | haematuria NOS === GRAPH WALKS === --- Walk 1 --- [6B22.Z] Olfactory reference disorder, unspecified --PARENT--> [6B22] Olfactory reference disorder Def: Olfactory Reference Disorder is characterised by persistent preoccupation with the belief that one is emitting a perceived foul or offensive body odour or breath that is either unnoticeable or only sl... --CHILD--> [6B22.Z] Olfactory reference disorder, unspecified --- Walk 2 --- [6B22.Z] Olfactory reference disorder, unspecified --PARENT--> [6B22] Olfactory reference disorder Def: Olfactory Reference Disorder is characterised by persistent preoccupation with the belief that one is emitting a perceived foul or offensive body odour or breath that is either unnoticeable or only sl... --CHILD--> [6B22.1] Olfactory reference disorder with poor to absent insight Def: All definitional requirements of olfactory reference disorder are met. Most or all of the time, the individual is convinced that the disorder-specific beliefs are true and cannot accept an alternative... --- Walk 3 --- [MB26.03] Delusion of reference Def: A delusion that events, objects, or other people in the person's immediate environment have a particular and unusual personal significance, usually of a negative or pejorative nature.... --PARENT--> [MB26.0] Delusion Def: A belief that is demonstrably untrue or not shared by others, usually based on incorrect inference about external reality. The belief is firmly held with conviction and is not, or is only briefly, sus... --PARENT--> [MB26] Symptoms or signs involving content of thought Def: Symptoms and signs involving content of thought include delusions, experiences of influence, passivity, and control, grandiosity, homicidal ideation, identity disturbance, obsessions, overvalued ideas... --- Walk 4 --- [MB26.03] Delusion of reference Def: A delusion that events, objects, or other people in the person's immediate environment have a particular and unusual personal significance, usually of a negative or pejorative nature.... --PARENT--> [MB26.0] Delusion Def: A belief that is demonstrably untrue or not shared by others, usually based on incorrect inference about external reality. The belief is firmly held with conviction and is not, or is only briefly, sus... --CHILD--> [MB26.01] Delusion of being controlled Def: A delusion that involves an external force or person controlling one's feelings, impulses, thoughts, or behaviour.... --- Walk 5 --- [6B22.1] Olfactory reference disorder with poor to absent insight Def: All definitional requirements of olfactory reference disorder are met. Most or all of the time, the individual is convinced that the disorder-specific beliefs are true and cannot accept an alternative... --PARENT--> [6B22] Olfactory reference disorder Def: Olfactory Reference Disorder is characterised by persistent preoccupation with the belief that one is emitting a perceived foul or offensive body odour or breath that is either unnoticeable or only sl... --CHILD--> [6B22.0] Olfactory reference disorder with fair to good insight Def: All definitional requirements of olfactory reference disorder are met. Much of the time, the individual is able to entertain the possibility that his or her disorder-specific beliefs may not be true a... --- Walk 6 --- [6B22.1] Olfactory reference disorder with poor to absent insight Def: All definitional requirements of olfactory reference disorder are met. Most or all of the time, the individual is convinced that the disorder-specific beliefs are true and cannot accept an alternative... --PARENT--> [6B22] Olfactory reference disorder Def: Olfactory Reference Disorder is characterised by persistent preoccupation with the belief that one is emitting a perceived foul or offensive body odour or breath that is either unnoticeable or only sl... --CHILD--> [6B22.Z] Olfactory reference disorder, unspecified
[ "[6B22.Z] Olfactory reference disorder, unspecified\n --PARENT--> [6B22] Olfactory reference disorder\n Def: Olfactory Reference Disorder is characterised by persistent preoccupation with the belief that one is emitting a perceived foul or offensive body odour or breath that is either unnoticeable or only sl...\n --CHILD--> [6B22.Z] Olfactory reference disorder, unspecified", "[6B22.Z] Olfactory reference disorder, unspecified\n --PARENT--> [6B22] Olfactory reference disorder\n Def: Olfactory Reference Disorder is characterised by persistent preoccupation with the belief that one is emitting a perceived foul or offensive body odour or breath that is either unnoticeable or only sl...\n --CHILD--> [6B22.1] Olfactory reference disorder with poor to absent insight\n Def: All definitional requirements of olfactory reference disorder are met. Most or all of the time, the individual is convinced that the disorder-specific beliefs are true and cannot accept an alternative...", "[MB26.03] Delusion of reference\n Def: A delusion that events, objects, or other people in the person's immediate environment have a particular and unusual personal significance, usually of a negative or pejorative nature....\n --PARENT--> [MB26.0] Delusion\n Def: A belief that is demonstrably untrue or not shared by others, usually based on incorrect inference about external reality. The belief is firmly held with conviction and is not, or is only briefly, sus...\n --PARENT--> [MB26] Symptoms or signs involving content of thought\n Def: Symptoms and signs involving content of thought include delusions, experiences of influence, passivity, and control, grandiosity, homicidal ideation, identity disturbance, obsessions, overvalued ideas...", "[MB26.03] Delusion of reference\n Def: A delusion that events, objects, or other people in the person's immediate environment have a particular and unusual personal significance, usually of a negative or pejorative nature....\n --PARENT--> [MB26.0] Delusion\n Def: A belief that is demonstrably untrue or not shared by others, usually based on incorrect inference about external reality. The belief is firmly held with conviction and is not, or is only briefly, sus...\n --CHILD--> [MB26.01] Delusion of being controlled\n Def: A delusion that involves an external force or person controlling one's feelings, impulses, thoughts, or behaviour....", "[6B22.1] Olfactory reference disorder with poor to absent insight\n Def: All definitional requirements of olfactory reference disorder are met. Most or all of the time, the individual is convinced that the disorder-specific beliefs are true and cannot accept an alternative...\n --PARENT--> [6B22] Olfactory reference disorder\n Def: Olfactory Reference Disorder is characterised by persistent preoccupation with the belief that one is emitting a perceived foul or offensive body odour or breath that is either unnoticeable or only sl...\n --CHILD--> [6B22.0] Olfactory reference disorder with fair to good insight\n Def: All definitional requirements of olfactory reference disorder are met. Much of the time, the individual is able to entertain the possibility that his or her disorder-specific beliefs may not be true a...", "[6B22.1] Olfactory reference disorder with poor to absent insight\n Def: All definitional requirements of olfactory reference disorder are met. Most or all of the time, the individual is convinced that the disorder-specific beliefs are true and cannot accept an alternative...\n --PARENT--> [6B22] Olfactory reference disorder\n Def: Olfactory Reference Disorder is characterised by persistent preoccupation with the belief that one is emitting a perceived foul or offensive body odour or breath that is either unnoticeable or only sl...\n --CHILD--> [6B22.Z] Olfactory reference disorder, unspecified" ]
6B22.Z
Olfactory reference disorder, unspecified
[ { "from_icd11": "6B22.Z", "icd10_code": "F428", "icd10_title": "Other obsessive-compulsive disorder" }, { "from_icd11": "3B63.1Z", "icd10_code": "D473", "icd10_title": "Essential (hemorrhagic) thrombocythemia" }, { "from_icd11": "MA14.1C", "icd10_code": "R760", "icd10_title": "Raised antibody titer" }, { "from_icd11": "3C0Z", "icd10_code": "D75A", "icd10_title": "Glucose-6-phosphate dehydrogenase (G6PD) deficiency without anemia" }, { "from_icd11": "3C0Z", "icd10_code": "D7581", "icd10_title": "Myelofibrosis" }, { "from_icd11": "3C0Z", "icd10_code": "D7582", "icd10_title": "Heparin induced thrombocytopenia (HIT)" }, { "from_icd11": "3C0Z", "icd10_code": "D7589", "icd10_title": "Other specified diseases of blood and blood-forming organs" }, { "from_icd11": "3C0Z", "icd10_code": "D759", "icd10_title": "Disease of blood and blood-forming organs, unspecified" }, { "from_icd11": "3C0Z", "icd10_code": "D763", "icd10_title": "Other histiocytosis syndromes" }, { "from_icd11": "3C0Z", "icd10_code": "Q899", "icd10_title": "Congenital malformation, unspecified" }, { "from_icd11": "3C0Z", "icd10_code": "III", "icd10_title": "" }, { "from_icd11": "3C0Z", "icd10_code": "D70-D77", "icd10_title": "" }, { "from_icd11": "3C0Z", "icd10_code": "D75", "icd10_title": "Other and unspecified diseases of blood and blood-forming organs" }, { "from_icd11": "3C0Z", "icd10_code": "D77", "icd10_title": "Other disorders of blood and blood-forming organs in diseases classified elsewhere" }, { "from_icd11": "3C0Z", "icd10_code": "D758", "icd10_title": "Other specified diseases of blood and blood-forming organs" } ]
F428
Other obsessive-compulsive disorder
In conclusion, we report the abrupt radiological response (correlated to neurological improvement), after only 6 days and four weeks of treatment with vemurafenib; the MRI follow-up showed further shrinkage and then stabilization in mass volume. To our knowledge, this is the first report assessing with consecutive MR images such a quick shrinkage in PLGGs treated with vemurafenib, highlighting the importance of an early investigation of BRAF status in all cases of LGG in children. We also wish to underline the pivotal role of neurosurgical biopsy for molecular diagnosis, in order to let a prompt BRAF mutations identification and guide subsequent targeted therapies. Being our first objective the rapid relief of symptoms due to tumor compression, such a remarkable result adds an important experience on the sparing of surgery-related procedures. The main limitations of this report are the ones expectedly pertaining to a case description involving a single or few patients, being PLGG a quite rare condition and vemurafenib having been adopted as a possible therapeutic strategy in pediatric tumors for a relatively short period. However, our cases demonstrate how a prompt radiological response to vemurafenib, and the related clinical improvement, can influence both therapeutic and surgical decisions, hopefully reducing the occurrence of second neurosurgery with associated risks of neurological sequelae.
4.125
0.577637
sec[2]/p[9]
en
0.999996
PMC9706968
https://doi.org/10.1186/s12887-022-03711-6
[ "vemurafenib", "radiological", "response", "neurological", "improvement", "shrinkage", "this", "braf", "cases", "prompt" ]
[ { "code": "QA00.B", "title": "Radiological examination" }, { "code": "PK8Y", "title": "Other specified surgical or other medical procedures associated with injury or harm in diagnostic or therapeutic use" }, { "code": "PK98.Z", "title": "Radiological devices associated with injury or harm, unspecified" }, { "code": "PK98.Y", "title": "Other specified radiological devices associated with injury or harm" }, { "code": "MG70", "title": "Abnormal diagnostic imaging results not elsewhere classified" }, { "code": "MB20.1", "title": "Coma" }, { "code": "4B4Z", "title": "Diseases of the immune system, unspecified" }, { "code": "MG46", "title": "Systemic inflammatory response syndrome of noninfectious origin" }, { "code": "MB72", "title": "Results of function studies of the nervous system" }, { "code": "MC81.0", "title": "Tachycardia, unspecified" } ]
=== ICD-11 CODES FOUND === [QA00.B] Radiological examination Also known as: Radiological examination | Routine chest X-ray Excludes: Special screening examination for neoplasm of breast [PK8Y] Other specified surgical or other medical procedures associated with injury or harm in diagnostic or therapeutic use Also known as: Other specified surgical or other medical procedures associated with injury or harm in diagnostic or therapeutic use | Diagnostic imaging procedures associated with injury or harm | complication of radiological procedure | radiological procedure associated with abnormal reaction of the patient, or of later complication, without mention of misadventure at the time of the procedure [PK98.Z] Radiological devices associated with injury or harm, unspecified Also known as: Radiological devices associated with injury or harm, unspecified | Radiological devices associated with injury or harm [PK98.Y] Other specified radiological devices associated with injury or harm Also known as: Other specified radiological devices associated with injury or harm [MG70] Abnormal diagnostic imaging results not elsewhere classified Also known as: Abnormal diagnostic imaging results not elsewhere classified | Abnormal radiological finding in skin and subcutaneous tissue | Mediastinal shift | mediastinum shift | Abnormal diagnostic imaging of genitourinary organs [MB20.1] Coma Definition: Acute state lasting more than one hour and usually less than a month. The comatose patient is unresponsive, lying with their eyes closed and cannot be aroused even by vigorous and noxious stimuli. Motor responses to noxious stimulation are limited to reflexive behaviour. Etiologies include but are not limited to traumatic, anoxic, infectious, neoplastic, vascular, inflammatory and metabolic brain injuries. Also known as: Coma | comatose | exanimation | Coma, NOS | Unconsciousness, NOS Excludes: Diabetic coma | Hepatic coma | Neonatal coma [4B4Z] Diseases of the immune system, unspecified Also known as: Diseases of the immune system, unspecified | immunological defect NOS | immunity disorder NOS | immune mechanism disorder NOS | immune compromised NOS [MG46] Systemic inflammatory response syndrome of noninfectious origin Also known as: Systemic inflammatory response syndrome of noninfectious origin | systemic inflammatory response syndrome NOS | SIRS -[systemic inflammatory response syndrome] of noninfectious origin | SIRS NOS -[systemic inflammatory response syndrome not otherwise specified] Excludes: Systemic inflammatory response syndrome of infectious origin [MB72] Results of function studies of the nervous system Also known as: Results of function studies of the nervous system | Abnormal results of function studies of central nervous system | abnormal central nervous system function studies | Abnormal brain function studies | Abnormal EEG - [electroencephalogram] [MC81.0] Tachycardia, unspecified Also known as: Tachycardia, unspecified | heart rate fast | rapid heart | Rapid heart beat | increased heart rate === GRAPH WALKS === --- Walk 1 --- [QA00.B] Radiological examination --EXCLUDES--> [?] Special screening examination for neoplasm of breast --EXCLUDES--> [?] Radiological examination --- Walk 2 --- [QA00.B] Radiological examination --PARENT--> [QA00] General examination or investigation of persons without complaint or reported diagnosis --EXCLUDES--> [?] Special screening examination for neoplasms --- Walk 3 --- [PK8Y] Other specified surgical or other medical procedures associated with injury or harm in diagnostic or therapeutic use --PARENT--> [?] Surgical or other medical procedures associated with injury or harm in diagnostic or therapeutic use --CHILD--> [PK8Y] Other specified surgical or other medical procedures associated with injury or harm in diagnostic or therapeutic use --- Walk 4 --- [PK8Y] Other specified surgical or other medical procedures associated with injury or harm in diagnostic or therapeutic use --PARENT--> [?] Surgical or other medical procedures associated with injury or harm in diagnostic or therapeutic use --CHILD--> [PK81] Certain medical procedures associated with injury or harm in therapeutic use --- Walk 5 --- [PK98.Z] Radiological devices associated with injury or harm, unspecified --PARENT--> [PK98] Radiological devices associated with injury or harm --CHILD--> [PK98.1] Radiological devices associated with injury or harm, therapeutic, nonsurgical or rehabilitative devices Def: A radiological device was involved in an adverse incident that occurred in a therapeutic (nonsurgical) and rehabilitative task... --- Walk 6 --- [PK98.Z] Radiological devices associated with injury or harm, unspecified --PARENT--> [PK98] Radiological devices associated with injury or harm --CHILD--> [PK98.1] Radiological devices associated with injury or harm, therapeutic, nonsurgical or rehabilitative devices Def: A radiological device was involved in an adverse incident that occurred in a therapeutic (nonsurgical) and rehabilitative task...
[ "[QA00.B] Radiological examination\n --EXCLUDES--> [?] Special screening examination for neoplasm of breast\n --EXCLUDES--> [?] Radiological examination", "[QA00.B] Radiological examination\n --PARENT--> [QA00] General examination or investigation of persons without complaint or reported diagnosis\n --EXCLUDES--> [?] Special screening examination for neoplasms", "[PK8Y] Other specified surgical or other medical procedures associated with injury or harm in diagnostic or therapeutic use\n --PARENT--> [?] Surgical or other medical procedures associated with injury or harm in diagnostic or therapeutic use\n --CHILD--> [PK8Y] Other specified surgical or other medical procedures associated with injury or harm in diagnostic or therapeutic use", "[PK8Y] Other specified surgical or other medical procedures associated with injury or harm in diagnostic or therapeutic use\n --PARENT--> [?] Surgical or other medical procedures associated with injury or harm in diagnostic or therapeutic use\n --CHILD--> [PK81] Certain medical procedures associated with injury or harm in therapeutic use", "[PK98.Z] Radiological devices associated with injury or harm, unspecified\n --PARENT--> [PK98] Radiological devices associated with injury or harm\n --CHILD--> [PK98.1] Radiological devices associated with injury or harm, therapeutic, nonsurgical or rehabilitative devices\n Def: A radiological device was involved in an adverse incident that occurred in a therapeutic (nonsurgical) and rehabilitative task...", "[PK98.Z] Radiological devices associated with injury or harm, unspecified\n --PARENT--> [PK98] Radiological devices associated with injury or harm\n --CHILD--> [PK98.1] Radiological devices associated with injury or harm, therapeutic, nonsurgical or rehabilitative devices\n Def: A radiological device was involved in an adverse incident that occurred in a therapeutic (nonsurgical) and rehabilitative task..." ]
QA00.B
Radiological examination
[ { "from_icd11": "QA00.B", "icd10_code": "Z016", "icd10_title": "" }, { "from_icd11": "PK8Y", "icd10_code": "Y848", "icd10_title": "Other medical procedures as the cause of abnormal reaction of the patient, or of later complication, without mention of misadventure at the time of the procedure" }, { "from_icd11": "PK8Y", "icd10_code": "Y832", "icd10_title": "Surgical operation with anastomosis, bypass or graft as the cause of abnormal reaction of the patient, or of later complication, without mention of misadventure at the time of the procedure" }, { "from_icd11": "PK98.Z", "icd10_code": "Y78", "icd10_title": "Radiological devices associated with adverse incidents" }, { "from_icd11": "MB20.1", "icd10_code": "R402142", "icd10_title": "Coma scale, eyes open, spontaneous, at arrival to emergency department" }, { "from_icd11": "MB20.1", "icd10_code": "R402362", "icd10_title": "Coma scale, best motor response, obeys commands, at arrival to emergency department" }, { "from_icd11": "MB20.1", "icd10_code": "R402252", "icd10_title": "Coma scale, best verbal response, oriented, at arrival to emergency department" }, { "from_icd11": "MB20.1", "icd10_code": "R402412", "icd10_title": "Glasgow coma scale score 13-15, at arrival to emergency department" }, { "from_icd11": "MB20.1", "icd10_code": "R4020", "icd10_title": "Unspecified coma" }, { "from_icd11": "MB20.1", "icd10_code": "R402141", "icd10_title": "Coma scale, eyes open, spontaneous, in the field [EMT or ambulance]" }, { "from_icd11": "MB20.1", "icd10_code": "R402361", "icd10_title": "Coma scale, best motor response, obeys commands, in the field [EMT or ambulance]" }, { "from_icd11": "MB20.1", "icd10_code": "R402251", "icd10_title": "Coma scale, best verbal response, oriented, in the field [EMT or ambulance]" }, { "from_icd11": "MB20.1", "icd10_code": "R402413", "icd10_title": "Glasgow coma scale score 13-15, at hospital admission" }, { "from_icd11": "MB20.1", "icd10_code": "R402143", "icd10_title": "Coma scale, eyes open, spontaneous, at hospital admission" }, { "from_icd11": "MB20.1", "icd10_code": "R402243", "icd10_title": "Coma scale, best verbal response, confused conversation, at hospital admission" } ]
Z016
CHS is often refractory to the standard treatment for nausea and vomiting . Unconventional antiemetics, such as haloperidol, have proved to be successful in alleviating symptoms; however, they can lead to adverse effects, such as dystonia, extrapyramidal reactions, and in rare cases, even to severe clinical pictures, such as neuroleptic malignant syndrome . The patient reported she was previously prescribed 1 mg oral haloperidol in a hospital setting, but had to discontinue shortly after due to the development of adverse effects. We treated her for 48 h with low doses of trazodone (100 mg/day) by i.v. infusion. This was followed by a benign clinical course and resolution of symptoms. At discharge, she consented to taking 150 mg of prolonged-release trazodone once daily in the evening for two weeks, and to increase it subsequently to 300 mg a day. The patient said she no longer had cravings for cannabis. She also immediately felt more relaxed and more focused on her academic activities. She was also advised to initiate a psychotherapy, but she refused. However, she agreed to undertake an online psychoeducation counseling course. At the 28 th week after her first visit, the patient was still continuing the prescribed therapy and reports she was abstaining from cannabis use. The patient reported no side effects while on trazodone. Laboratory examinations revealed no alterations or off-normal values.
3.917969
0.96875
sec[1]/sec[2]/p[1]
en
0.999998
PMC9224499
https://doi.org/10.3390/ijerph19127397
[ "effects", "trazodone", "haloperidol", "however", "adverse", "prescribed", "course", "cannabis", "often", "refractory" ]
[ { "code": "NF09", "title": "Adverse effects, not elsewhere classified" }, { "code": "NE60", "title": "Harmful effects of drugs, medicaments or biological substances, not elsewhere classified" }, { "code": "NE6Z", "title": "Harmful effects of unspecified substance" }, { "code": "NE61", "title": "Harmful effects of or exposure to noxious substances, chiefly nonmedicinal as to source, not elsewhere classified" }, { "code": "NF08.2Z", "title": "Effects of vibration, unspecified" }, { "code": "NF0Y", "title": "Other specified effects of external causes" }, { "code": "EH7Z", "title": "Unspecified adverse cutaneous reactions to medication" }, { "code": "MB41.2", "title": "Dysgeusia" }, { "code": "PL13.0", "title": "Overdose of substance, as mode of injury or harm" }, { "code": "PL13.3", "title": "Incorrect substance, as mode of injury or harm" } ]
=== ICD-11 CODES FOUND === [NF09] Adverse effects, not elsewhere classified Definition: Adverse effects which cannot be attributed to any more specific cause and thus excluding but not limited to injury, allergy, hypersensitivity, toxic effects and complications of surgical and medical care. Also known as: Adverse effects, not elsewhere classified | adverse effects, unspecified Excludes: Injury or harm arising from surgical or medical care, not elsewhere classified | Anaphylaxis | anaphylactic shock due to serum [NE60] Harmful effects of drugs, medicaments or biological substances, not elsewhere classified Also known as: Harmful effects of drugs, medicaments or biological substances, not elsewhere classified | drugs, medicaments or biological substances, toxicity not elsewhere classified | adverse drug effects | drug reaction NOS | drug allergy NOS Excludes: Alcohol intoxication | pathological drug intoxication | hypersensitivity reaction to correctly administered drug [NE6Z] Harmful effects of unspecified substance Also known as: Harmful effects of unspecified substance | poisoning NOS | Sequelae of poisoning by drugs, medicaments or biological substances | late effect of poisoning by drugs, medicaments or biological substances | Sequelae of toxic effects of substances chiefly nonmedicinal as to source [NE61] Harmful effects of or exposure to noxious substances, chiefly nonmedicinal as to source, not elsewhere classified Also known as: Harmful effects of or exposure to noxious substances, chiefly nonmedicinal as to source, not elsewhere classified | Harmful effects of or exposure to noxious substances chiefly nonmedicinal as to source, alcohols | alcohol poisoning | alcohol toxicity | Harmful effects of or exposure to noxious substances chiefly nonmedicinal as to source, Ethanol Excludes: corrosions | Bacterial foodborne intoxications [NF08.2Z] Effects of vibration, unspecified Also known as: Effects of vibration, unspecified | Effects of vibration [NF0Y] Other specified effects of external causes Also known as: Other specified effects of external causes | Adverse effect physical factor | Jet lag | Environmental exposure, not elsewhere classified | exposure NOS [EH7Z] Unspecified adverse cutaneous reactions to medication Also known as: Unspecified adverse cutaneous reactions to medication [MB41.2] Dysgeusia Definition: A disorder characterised by an alteration of the sense of taste Also known as: Dysgeusia | parageusia | loss of taste sense | disturbance of taste | cacogeusia Includes: cacogeusia | ageusia [PL13.0] Overdose of substance, as mode of injury or harm Definition: Incorrect dose - too high Also known as: Overdose of substance, as mode of injury or harm | wrong dose of substance as mode of injury | wrong strength of substance as mode of injury | dose of substance administered or taken too early or too quickly as a mode of injury | extra dose of substance administered as mode of injury Includes: overdose of prescribed drug | medication error leading to excess level or effect of prescribed drug Excludes: Overdose of substance without injury or harm | Unintentional exposure to or harmful effects of drugs, medicaments or biological substances | Intentional self-harm by exposure to or harmful effects of drugs, medicaments or biological substances [PL13.3] Incorrect substance, as mode of injury or harm Also known as: Incorrect substance, as mode of injury or harm | wrong drug or product given by healthcare provider as mode of injury | incorrect substance given as result of prescribing error | wrong drug given as result of prescribing error | incorrect substance or drug as result of administration error === GRAPH WALKS === --- Walk 1 --- [NF09] Adverse effects, not elsewhere classified Def: Adverse effects which cannot be attributed to any more specific cause and thus excluding but not limited to injury, allergy, hypersensitivity, toxic effects and complications of surgical and medical c... --EXCLUDES--> [?] Other serum reactions --CHILD--> [?] Serum sickness vasculitis Def: An acute vasculitic illness typified by fever, arthralgia and urticarial vasculitis resulting from an immune complex-mediated (type III) immune reaction to foreign protein. Historically this was large... --- Walk 2 --- [NF09] Adverse effects, not elsewhere classified Def: Adverse effects which cannot be attributed to any more specific cause and thus excluding but not limited to injury, allergy, hypersensitivity, toxic effects and complications of surgical and medical c... --EXCLUDES--> [?] Injury or harm arising from surgical or medical care, not elsewhere classified --PARENT--> [?] Injury, poisoning or certain other consequences of external causes Def: !markdown In the ICD, injury means physical or physiological bodily harm resulting from interaction of the body with energy (mechanical, thermal, electrical, chemical or radiant, or due to extreme pre... --- Walk 3 --- [NE60] Harmful effects of drugs, medicaments or biological substances, not elsewhere classified --EXCLUDES--> [?] Allergic or hypersensitivity conditions Def: Allergy is a hypersensitivity reaction initiated by proven immunologic mechanisms. Hypersensitivity is defined as conditions clinically resembling allergy that cause objectively reproducible symptoms... --PARENT--> [?] Diseases of the immune system --- Walk 4 --- [NE60] Harmful effects of drugs, medicaments or biological substances, not elsewhere classified --EXCLUDES--> [?] Allergic or hypersensitivity conditions Def: Allergy is a hypersensitivity reaction initiated by proven immunologic mechanisms. Hypersensitivity is defined as conditions clinically resembling allergy that cause objectively reproducible symptoms... --CHILD--> [?] Allergic or hypersensitivity disorders involving the eye Def: Allergic or hypersensitivity disorders involving the eye includes several clinically different conditions that can be considered as hypersensitivity disorders of the ocular surface. The classification... --- Walk 5 --- [NE6Z] Harmful effects of unspecified substance --PARENT--> [?] Harmful effects of substances --CHILD--> [NE60] Harmful effects of drugs, medicaments or biological substances, not elsewhere classified --- Walk 6 --- [NE6Z] Harmful effects of unspecified substance --PARENT--> [?] Harmful effects of substances --CHILD--> [NE60] Harmful effects of drugs, medicaments or biological substances, not elsewhere classified
[ "[NF09] Adverse effects, not elsewhere classified\n Def: Adverse effects which cannot be attributed to any more specific cause and thus excluding but not limited to injury, allergy, hypersensitivity, toxic effects and complications of surgical and medical c...\n --EXCLUDES--> [?] Other serum reactions\n --CHILD--> [?] Serum sickness vasculitis\n Def: An acute vasculitic illness typified by fever, arthralgia and urticarial vasculitis resulting from an immune complex-mediated (type III) immune reaction to foreign protein. Historically this was large...", "[NF09] Adverse effects, not elsewhere classified\n Def: Adverse effects which cannot be attributed to any more specific cause and thus excluding but not limited to injury, allergy, hypersensitivity, toxic effects and complications of surgical and medical c...\n --EXCLUDES--> [?] Injury or harm arising from surgical or medical care, not elsewhere classified\n --PARENT--> [?] Injury, poisoning or certain other consequences of external causes\n Def: !markdown\nIn the ICD, injury means physical or physiological bodily harm resulting from interaction of the body with energy (mechanical, thermal, electrical, chemical or radiant, or due to extreme pre...", "[NE60] Harmful effects of drugs, medicaments or biological substances, not elsewhere classified\n --EXCLUDES--> [?] Allergic or hypersensitivity conditions\n Def: Allergy is a hypersensitivity reaction initiated by proven immunologic mechanisms.\n\nHypersensitivity is defined as conditions clinically resembling allergy that cause objectively reproducible symptoms...\n --PARENT--> [?] Diseases of the immune system", "[NE60] Harmful effects of drugs, medicaments or biological substances, not elsewhere classified\n --EXCLUDES--> [?] Allergic or hypersensitivity conditions\n Def: Allergy is a hypersensitivity reaction initiated by proven immunologic mechanisms.\n\nHypersensitivity is defined as conditions clinically resembling allergy that cause objectively reproducible symptoms...\n --CHILD--> [?] Allergic or hypersensitivity disorders involving the eye\n Def: Allergic or hypersensitivity disorders involving the eye includes several clinically different conditions that can be considered as hypersensitivity disorders of the ocular surface. The classification...", "[NE6Z] Harmful effects of unspecified substance\n --PARENT--> [?] Harmful effects of substances\n --CHILD--> [NE60] Harmful effects of drugs, medicaments or biological substances, not elsewhere classified", "[NE6Z] Harmful effects of unspecified substance\n --PARENT--> [?] Harmful effects of substances\n --CHILD--> [NE60] Harmful effects of drugs, medicaments or biological substances, not elsewhere classified" ]
NF09
Adverse effects, not elsewhere classified
[ { "from_icd11": "NF09", "icd10_code": "T7601XA", "icd10_title": "Adult neglect or abandonment, suspected, initial encounter" }, { "from_icd11": "NF09", "icd10_code": "T7621XA", "icd10_title": "Adult sexual abuse, suspected, initial encounter" }, { "from_icd11": "NF09", "icd10_code": "T7691XA", "icd10_title": "Unspecified adult maltreatment, suspected, initial encounter" }, { "from_icd11": "NF09", "icd10_code": "T7611XA", "icd10_title": "Adult physical abuse, suspected, initial encounter" }, { "from_icd11": "NF09", "icd10_code": "T7621XS", "icd10_title": "Adult sexual abuse, suspected, sequela" }, { "from_icd11": "NF09", "icd10_code": "T7631XA", "icd10_title": "Adult psychological abuse, suspected, initial encounter" }, { "from_icd11": "NF09", "icd10_code": "T7601XD", "icd10_title": "Adult neglect or abandonment, suspected, subsequent encounter" }, { "from_icd11": "NF09", "icd10_code": "T788XXA", "icd10_title": "Other adverse effects, not elsewhere classified, initial encounter" }, { "from_icd11": "NF09", "icd10_code": "T781XXS", "icd10_title": "Other adverse food reactions, not elsewhere classified, sequela" }, { "from_icd11": "NF09", "icd10_code": "T788XXS", "icd10_title": "Other adverse effects, not elsewhere classified, sequela" }, { "from_icd11": "NF09", "icd10_code": "T76", "icd10_title": "Adult and child abuse, neglect and other maltreatment, suspected" }, { "from_icd11": "NF09", "icd10_code": "T78", "icd10_title": "Adverse effects, not elsewhere classified" }, { "from_icd11": "NF09", "icd10_code": "T781", "icd10_title": "Other adverse food reactions, not elsewhere classified" }, { "from_icd11": "NF09", "icd10_code": "T788", "icd10_title": "Other adverse effects, not elsewhere classified" }, { "from_icd11": "NF09", "icd10_code": "T789", "icd10_title": "" } ]
T7601XA
Adult neglect or abandonment, suspected, initial encounter
Abdominal color Doppler ultrasonography showed a large amount of abdominal flatulence. The local intestinal structure of the left lower abdomen was slightly disordered, and necrotizing enterocolitis was indicated. Ultrasonographic examination of the abdominal aorta, bilateral neck arteries, and veins showed no abnormality. Color Doppler ultrasonography of the liver, gallbladder, pancreas spleen, and kidneys showed no abnormality. The results of routine stool tests and occult blood tests were weakly positive. procalcitonin level was 0.18 ng/mL, and urine amylase had no abnormality. Blood gas analysis showed the following results: pH 7.38, PCO2 33.1 mmHg, PO2 84.4 mmHg, BE-5.5 mmol/L, lactic acid 5.8 mmol/L, blood glucose 8.1 mmol/L. The blood biochemistry test showed the following results: K + 5.23 mmol/L, Na + 130 mmol/L, Cl − 103 mmol/L, HCO3 − <5.0 mmol/L. Blood routine test showed the following results: white blood cells 18.22 × 10 9 /L, red blood cells 1.97 × 10 12 /L, hemoglobin 130 g/L, platelets 361 × 10 9 /L, lymphocyte percentage 40.0%, monocytes 11.0%, neutrophils 45.0%. When a blood sample was taken from the infant, his blood was pink serous, and the upper layer showed milky white cream, indicating severe hyperlipidemia, but could not be detected by liver function, kidney function, myocardial enzyme, blood lipid, blood amylase, coagulation routine, D -dimer, and other laboratory tests.
3.884766
0.918945
sec[1]/p[2]
en
0.999998
35960041
https://doi.org/10.1097/MD.0000000000029689
[ "blood", "mmol", "abdominal", "abnormality", "routine", "color", "doppler", "ultrasonography", "liver", "amylase" ]
[ { "code": "3C0Z", "title": "Diseases of the blood or blood-forming organs, unspecified" }, { "code": "MF50.4Z", "title": "Haematuria, unspecified" }, { "code": "MA12.1", "title": "Finding of cocaine in blood" }, { "code": "MA12.4", "title": "Finding of steroid agent in blood" }, { "code": "MA12.2", "title": "Finding of hallucinogen in blood" }, { "code": "GB42.1", "title": "Albuminuria, Grade A3" }, { "code": "GB42.0", "title": "Albuminuria, Grade A2" }, { "code": "MA18.0Y", "title": "Other specified elevated blood glucose level" }, { "code": "MD81.3", "title": "Acute abdomen" }, { "code": "JA01.0", "title": "Abdominal pregnancy" } ]
=== ICD-11 CODES FOUND === [3C0Z] Diseases of the blood or blood-forming organs, unspecified Also known as: Diseases of the blood or blood-forming organs, unspecified | Blood, lymph or spleen disease | blood condition NOS | blood disorder NOS | bone marrow disease NOS [MF50.4Z] Haematuria, unspecified Also known as: Haematuria, unspecified | Haematuria | blood in urine | urinary blood | haematuria NOS [MA12.1] Finding of cocaine in blood Also known as: Finding of cocaine in blood | cocaine in blood [MA12.4] Finding of steroid agent in blood Also known as: Finding of steroid agent in blood | steroid in blood [MA12.2] Finding of hallucinogen in blood Also known as: Finding of hallucinogen in blood | hallucinogen in blood [GB42.1] Albuminuria, Grade A3 Definition: Presence of excessive albumin in the urine, indicating abnormal permeability glomerular filtration. Can be quantitated by either timed collections or spot urine samples with the concentration adjusted to the urine creatinine concentration to correct for variations in overall urine concentration. When persistent and of moderate or greater severity usually indicates overt glomerular disease such as caused by diabetic glomerulosclerosis, glomerulonephritis or amyloid. Also known as: Albuminuria, Grade A3 | albuminuria >30 mg/mmol creatinine | macroalbuminuria | overt albuminuria | overt nephropathy [GB42.0] Albuminuria, Grade A2 Definition: Presence of excessive albumin in the urine, indicating abnormal permeability glomerular filtration. Can be quantitated by either timed collections or spot urine samples with the concentration adjusted to the urine creatinine concentration to correct for variations in overall urine concentration. When persistent and of moderate or greater severity usually indicates overt glomerular disease such as caused by diabetic glomerulosclerosis, glomerulonephritis or amyloid. Also known as: Albuminuria, Grade A2 | microalbuminuria | incipient nephropathy | mild to moderate albuminuria | albuminuria 3-30 mg/mmol creatinine [MA18.0Y] Other specified elevated blood glucose level Also known as: Other specified elevated blood glucose level | Blood glucose between 8.0 - 11.9 mmol/L pre-meal or fasting | Blood glucose between 12.0 - 13.9 mmol/L pre-meal or fasting | Blood glucose greater than or equal to 14.0 mmol/L pre-meal or fasting | Blood glucose between 12.0 - 13.9 mmol/L post-meal or not otherwise specified [MD81.3] Acute abdomen Definition: A clinical syndrome with acute abdominal pain that is severe, and rapid onset. Acute abdomen may be caused by a variety of disorders, injuries, or diseases Also known as: Acute abdomen | acute abdominal pain syndrome | surgical abdomen | abdominal acute syndrome | severe abdomen pain [JA01.0] Abdominal pregnancy Definition: A condition characterised by implantation of the embryo within the peritoneal cavity during pregnancy. Also known as: Abdominal pregnancy | abdomen pregnancy | intraperitoneal pregnancy Excludes: Maternal care for viable fetus in abdominal pregnancy | Delivery of viable fetus in abdominal pregnancy === GRAPH WALKS === --- Walk 1 --- [3C0Z] Diseases of the blood or blood-forming organs, unspecified --PARENT--> [03] Diseases of the blood or blood-forming organs Def: This chapter includes diseases of the blood as well as diseases of blood forming organs.... --CHILD--> [?] Coagulation defects, purpura or other haemorrhagic or related conditions Def: A condition caused by determinants arising during the antenatal period, after birth or by genetically inherited factors, leading to coagulation defects. This condition is characterised by increased br... --- Walk 2 --- [3C0Z] Diseases of the blood or blood-forming organs, unspecified --PARENT--> [03] Diseases of the blood or blood-forming organs Def: This chapter includes diseases of the blood as well as diseases of blood forming organs.... --EXCLUDES--> [?] Certain conditions originating in the perinatal period Def: This chapter includes conditions that have their origin in the perinatal period even though death or morbidity occurs later.... --- Walk 3 --- [MF50.4Z] Haematuria, unspecified --PARENT--> [MF50.4] Haematuria Def: Hematuria means presence of blood or red blood cells (RBCs) in the urine. There are two types of hematuria: gross hematuria (when one can see the blood in the urine) and microscopic hematuria (when th... --PARENT--> [MF50] Abnormal micturition --- Walk 4 --- [MF50.4Z] Haematuria, unspecified --PARENT--> [MF50.4] Haematuria Def: Hematuria means presence of blood or red blood cells (RBCs) in the urine. There are two types of hematuria: gross hematuria (when one can see the blood in the urine) and microscopic hematuria (when th... --CHILD--> [MF50.4Z] Haematuria, unspecified --- Walk 5 --- [MA12.1] Finding of cocaine in blood --PARENT--> [MA12] Clinical findings of drugs, medicaments and biological substances in blood, blood-forming organs, or the immune system --CHILD--> [MA12.2] Finding of hallucinogen in blood --- Walk 6 --- [MA12.1] Finding of cocaine in blood --PARENT--> [MA12] Clinical findings of drugs, medicaments and biological substances in blood, blood-forming organs, or the immune system --CHILD--> [MA12.2] Finding of hallucinogen in blood
[ "[3C0Z] Diseases of the blood or blood-forming organs, unspecified\n --PARENT--> [03] Diseases of the blood or blood-forming organs\n Def: This chapter includes diseases of the blood as well as diseases of blood forming organs....\n --CHILD--> [?] Coagulation defects, purpura or other haemorrhagic or related conditions\n Def: A condition caused by determinants arising during the antenatal period, after birth or by genetically inherited factors, leading to coagulation defects. This condition is characterised by increased br...", "[3C0Z] Diseases of the blood or blood-forming organs, unspecified\n --PARENT--> [03] Diseases of the blood or blood-forming organs\n Def: This chapter includes diseases of the blood as well as diseases of blood forming organs....\n --EXCLUDES--> [?] Certain conditions originating in the perinatal period\n Def: This chapter includes conditions that have their origin in the perinatal period even though death or morbidity occurs later....", "[MF50.4Z] Haematuria, unspecified\n --PARENT--> [MF50.4] Haematuria\n Def: Hematuria means presence of blood or red blood cells (RBCs) in the urine. There are two types of hematuria: gross hematuria (when one can see the blood in the urine) and microscopic hematuria (when th...\n --PARENT--> [MF50] Abnormal micturition", "[MF50.4Z] Haematuria, unspecified\n --PARENT--> [MF50.4] Haematuria\n Def: Hematuria means presence of blood or red blood cells (RBCs) in the urine. There are two types of hematuria: gross hematuria (when one can see the blood in the urine) and microscopic hematuria (when th...\n --CHILD--> [MF50.4Z] Haematuria, unspecified", "[MA12.1] Finding of cocaine in blood\n --PARENT--> [MA12] Clinical findings of drugs, medicaments and biological substances in blood, blood-forming organs, or the immune system\n --CHILD--> [MA12.2] Finding of hallucinogen in blood", "[MA12.1] Finding of cocaine in blood\n --PARENT--> [MA12] Clinical findings of drugs, medicaments and biological substances in blood, blood-forming organs, or the immune system\n --CHILD--> [MA12.2] Finding of hallucinogen in blood" ]
3C0Z
Diseases of the blood or blood-forming organs, unspecified
[ { "from_icd11": "3C0Z", "icd10_code": "D75A", "icd10_title": "Glucose-6-phosphate dehydrogenase (G6PD) deficiency without anemia" }, { "from_icd11": "3C0Z", "icd10_code": "D7581", "icd10_title": "Myelofibrosis" }, { "from_icd11": "3C0Z", "icd10_code": "D7582", "icd10_title": "Heparin induced thrombocytopenia (HIT)" }, { "from_icd11": "3C0Z", "icd10_code": "D7589", "icd10_title": "Other specified diseases of blood and blood-forming organs" }, { "from_icd11": "3C0Z", "icd10_code": "D759", "icd10_title": "Disease of blood and blood-forming organs, unspecified" }, { "from_icd11": "3C0Z", "icd10_code": "D763", "icd10_title": "Other histiocytosis syndromes" }, { "from_icd11": "3C0Z", "icd10_code": "Q899", "icd10_title": "Congenital malformation, unspecified" }, { "from_icd11": "3C0Z", "icd10_code": "III", "icd10_title": "" }, { "from_icd11": "3C0Z", "icd10_code": "D70-D77", "icd10_title": "" }, { "from_icd11": "3C0Z", "icd10_code": "D75", "icd10_title": "Other and unspecified diseases of blood and blood-forming organs" }, { "from_icd11": "3C0Z", "icd10_code": "D77", "icd10_title": "Other disorders of blood and blood-forming organs in diseases classified elsewhere" }, { "from_icd11": "3C0Z", "icd10_code": "D758", "icd10_title": "Other specified diseases of blood and blood-forming organs" }, { "from_icd11": "3C0Z", "icd10_code": "D76", "icd10_title": "Other specified diseases with participation of lymphoreticular and reticulohistiocytic tissue" }, { "from_icd11": "MF50.4Z", "icd10_code": "R310", "icd10_title": "Gross hematuria" }, { "from_icd11": "MF50.4Z", "icd10_code": "R312", "icd10_title": "Other microscopic hematuria" } ]
D75A
Glucose-6-phosphate dehydrogenase (G6PD) deficiency without anemia
Patient I:2. The proband presented complaining of blurred vision on distance and night blindness. The patient has a moderate myopia and BCVA was 0.63 in the right eye and 1.00 in the left eye. The patient presented a severe color defect at the Ishihara test. Anterior segment examination showed a bilateral lens opacification. Fundus examination showed a large bilateral chorioretinal atrophy, large peripheral pigmentary rearrangements and focal areas of Retinal Pigment Epithelium (RPE) disruption with light sparring of central macula pigmentation, especially in the left eye . A SD-OCT was performed, showing extensive chorioretinal atrophy and retinal thinning in the right eye with hyper-transmission posterior to the RPE, while, in the left eye, a residual central island of preserved Ellipsoid Zone (EZ) area was present, with chorioretinal atrophy in the superior area of the macula. Pseudodendritic outer retinal tubulations (ORT) were present in the context of the chorioretinal atrophy in the left eye . Areas of residual RPE could also be visualized in Infrared Reflectance (IR) images, mostly in the left eye compared to the right eye . FAF images in both eyes showed generalized decreased autofluorescence, with residual areas of autofluorescence in the central macular area in the right eye with a male resembling pattern and also in the temporal macular area in the left eye with a geographic pattern .
4.089844
0.970703
sec[2]/sec[0]/p[1]
en
0.999997
PMC9321261
https://doi.org/10.3390/genes13071268
[ "chorioretinal", "atrophy", "area", "areas", "retinal", "residual", "large", "macula", "present", "autofluorescence" ]
[ { "code": "9B65.Z", "title": "Posterior uveitis, unspecified" }, { "code": "9B60", "title": "Choroidal degeneration" }, { "code": "9B70", "title": "Inherited retinal dystrophies" }, { "code": "9B62", "title": "Chorioretinal scars" }, { "code": "LA13.1", "title": "Coloboma of choroid or retina" }, { "code": "FB32.Y", "title": "Other specified disorders of muscles" }, { "code": "BE2Y", "title": "Other specified diseases of the circulatory system" }, { "code": "CB40.Y", "title": "Other specified diseases of the respiratory system" }, { "code": "9C40.BZ", "title": "Optic atrophy, unspecified" }, { "code": "8E7Y", "title": "Other specified diseases of the nervous system" } ]
=== ICD-11 CODES FOUND === [9B65.Z] Posterior uveitis, unspecified Also known as: Posterior uveitis, unspecified | Posterior uveitis | Chorioretinitis | Retinochoroiditis | Choroiditis [9B60] Choroidal degeneration Also known as: Choroidal degeneration | degenerative choroidopathy | chorioretinal degeneration | hereditary chorioretinal degeneration | hereditary degeneration of choroid Excludes: angioid streaks [9B70] Inherited retinal dystrophies Also known as: Inherited retinal dystrophies | hereditary retinal dystrophies | Amaurosis - hypertrichosis | Autosomal dominant late-onset retinal degeneration | Bothnia retinal dystrophy Includes: Leber congenital amaurosis | Stargardt disease | Vitreoretinal dystrophy [9B62] Chorioretinal scars Also known as: Chorioretinal scars | chorioretinal cicatrix | cicatrix of choroid | choroid scar | macula scar Includes: Macula scars of posterior pole | Solar retinopathy [LA13.1] Coloboma of choroid or retina Definition: A condition of the eye characterised by absence of the retina in the lower inside corner of the eye. Also known as: Coloboma of choroid or retina | chorioretinal coloboma | Coloboma of choroid or retina, unilateral | Coloboma of choroid or retina, bilateral [FB32.Y] Other specified disorders of muscles Also known as: Other specified disorders of muscles | Muscle wasting or atrophy, not elsewhere classified | muscle wasting | muscle wasting disorder | Sarcopenia [BE2Y] Other specified diseases of the circulatory system Also known as: Other specified diseases of the circulatory system | Certain specified forms of heart disease | Cardiac disorder, unspecified | disorder of heart NOS | organic disease or disorder of heart [CB40.Y] Other specified diseases of the respiratory system Also known as: Other specified diseases of the respiratory system | Secondary respiratory disorders | Respiratory disorders in diseases classified elsewhere | Diseases of bronchus, not elsewhere classified | Acquired bronchial diverticulum [9C40.BZ] Optic atrophy, unspecified Also known as: Optic atrophy, unspecified | Optic atrophy | optic nerve atrophy | Primary optic atrophy | OA - [optic atrophy] [8E7Y] Other specified diseases of the nervous system Also known as: Other specified diseases of the nervous system | Circumscribed brain atrophy | circumscribed cerebral atrophy | atrophic lobar sclerosis | atrophic lobar brain sclerosis === GRAPH WALKS === --- Walk 1 --- [9B65.Z] Posterior uveitis, unspecified --PARENT--> [9B65] Posterior uveitis --CHILD--> [9B65.Z] Posterior uveitis, unspecified --- Walk 2 --- [9B65.Z] Posterior uveitis, unspecified --PARENT--> [9B65] Posterior uveitis --CHILD--> [9B65.0] Noninfectious posterior uveitis --- Walk 3 --- [9B60] Choroidal degeneration --EXCLUDES--> [?] Degeneration of macula or posterior pole --EXCLUDES--> [?] Age-related macular degeneration Def: Age-related macular degeneration (ARMD) is defined as an ocular disease leading to loss of central vision in the elderly, and characterised by primary and secondary damage of macular retinal pigment e... --- Walk 4 --- [9B60] Choroidal degeneration --EXCLUDES--> [?] Degeneration of macula or posterior pole --PARENT--> [?] Certain specified retinal disorders --- Walk 5 --- [9B70] Inherited retinal dystrophies --RELATED_TO--> [?] Usher syndrome Def: Usher syndrome is the most common cause of hereditary combined deafness-blindness, and is characterised by the association of sensorineural deafness (usually congenital) with retinitis pigmentosa and ... --PARENT--> [?] Syndromic genetic deafness --- Walk 6 --- [9B70] Inherited retinal dystrophies --RELATED_TO--> [?] Sjögren-Larsson syndrome Def: Sjögren-Larsson syndrome is a neurocutaneous disorder caused by an inborn error of lipid metabolism and characterised by congenital ichthyosis, intellectual deficit, and spasticity.... --PARENT--> [?] Other disorders of fatty acid oxidation or ketone body metabolism
[ "[9B65.Z] Posterior uveitis, unspecified\n --PARENT--> [9B65] Posterior uveitis\n --CHILD--> [9B65.Z] Posterior uveitis, unspecified", "[9B65.Z] Posterior uveitis, unspecified\n --PARENT--> [9B65] Posterior uveitis\n --CHILD--> [9B65.0] Noninfectious posterior uveitis", "[9B60] Choroidal degeneration\n --EXCLUDES--> [?] Degeneration of macula or posterior pole\n --EXCLUDES--> [?] Age-related macular degeneration\n Def: Age-related macular degeneration (ARMD) is defined as an ocular disease leading to loss of central vision in the elderly, and characterised by primary and secondary damage of macular retinal pigment e...", "[9B60] Choroidal degeneration\n --EXCLUDES--> [?] Degeneration of macula or posterior pole\n --PARENT--> [?] Certain specified retinal disorders", "[9B70] Inherited retinal dystrophies\n --RELATED_TO--> [?] Usher syndrome\n Def: Usher syndrome is the most common cause of hereditary combined deafness-blindness, and is characterised by the association of sensorineural deafness (usually congenital) with retinitis pigmentosa and ...\n --PARENT--> [?] Syndromic genetic deafness", "[9B70] Inherited retinal dystrophies\n --RELATED_TO--> [?] Sjögren-Larsson syndrome\n Def: Sjögren-Larsson syndrome is a neurocutaneous disorder caused by an inborn error of lipid metabolism and characterised by congenital ichthyosis, intellectual deficit, and spasticity....\n --PARENT--> [?] Other disorders of fatty acid oxidation or ketone body metabolism" ]
9B65.Z
Posterior uveitis, unspecified
[ { "from_icd11": "9B60", "icd10_code": "H31102", "icd10_title": "Choroidal degeneration, unspecified, left eye" }, { "from_icd11": "9B60", "icd10_code": "H31103", "icd10_title": "Choroidal degeneration, unspecified, bilateral" }, { "from_icd11": "9B60", "icd10_code": "H311", "icd10_title": "Choroidal degeneration" }, { "from_icd11": "9B70", "icd10_code": "H3552", "icd10_title": "Pigmentary retinal dystrophy" }, { "from_icd11": "9B70", "icd10_code": "H3550", "icd10_title": "Unspecified hereditary retinal dystrophy" }, { "from_icd11": "9B70", "icd10_code": "H3553", "icd10_title": "Other dystrophies primarily involving the sensory retina" }, { "from_icd11": "9B70", "icd10_code": "H3554", "icd10_title": "Dystrophies primarily involving the retinal pigment epithelium" }, { "from_icd11": "9B70", "icd10_code": "H355", "icd10_title": "Hereditary retinal dystrophy" }, { "from_icd11": "9B62", "icd10_code": "H31009", "icd10_title": "Unspecified chorioretinal scars, unspecified eye" }, { "from_icd11": "9B62", "icd10_code": "H31001", "icd10_title": "Unspecified chorioretinal scars, right eye" }, { "from_icd11": "9B62", "icd10_code": "H310", "icd10_title": "Chorioretinal scars" }, { "from_icd11": "FB32.Y", "icd10_code": "M6281", "icd10_title": "Muscle weakness (generalized)" }, { "from_icd11": "9C40.BZ", "icd10_code": "H47213", "icd10_title": "Primary optic atrophy, bilateral" }, { "from_icd11": "9C40.BZ", "icd10_code": "H47291", "icd10_title": "Other optic atrophy, right eye" }, { "from_icd11": "9C40.BZ", "icd10_code": "H47292", "icd10_title": "Other optic atrophy, left eye" } ]
H31102
Choroidal degeneration, unspecified, left eye
In the intensive care unit (ICU), she was given nothing by mouth (NPO) and started on total parenteral nutrition, broad-spectrum IV antibiotics for 7 days, and IV proton pump inhibitor therapy. Post-ablation, anticoagulation was continued with IV unfractionated heparin. Based on the patient’s clinical stability and following interdisciplinary discussion between the surgical and cardiac electrophysiology teams, the decision was made to continue a conservative management approach with close observation and frequent reassessment of symptoms and hemodynamics. On day 7 after admission, CT and EGD were again performed, which showed 2 esophageal injuries with ulceration and permeating fibrin around the injury. A nasal enteric tube was introduced under direct visualization during the endoscopy. On day 8, the patient was tolerating parenteral nutrition, was afebrile and normotensive, and her CRP level had downtrended, so she was transferred from the ICU to a medical floor. At day 22, the patient had no worsening of her clinical condition and an additional repeat EGD showed complete healing of one of the esophageal injuries, a closure of about 50% of the previously damaged area, and the presence of granulation tissue . The patient remained hospitalized for further monitoring and patient preference. On inpatient day 46, EGD revealed complete healing of the esophageal injury , and the patient was discharged.
3.568359
0.978516
sec[1]/p[0]
en
0.999999
36196233
https://doi.org/10.19102/icrm.2022.130904
[ "esophageal", "parenteral", "nutrition", "injuries", "injury", "complete", "healing", "intensive", "unit", "nothing" ]
[ { "code": "DA2Z", "title": "Diseases of oesophagus, unspecified" }, { "code": "DA24.Z", "title": "Oesophagitis, unspecified" }, { "code": "DA20.0", "title": "Oesophageal obstruction" }, { "code": "DA25.Z", "title": "Oesophageal ulcer, unspecified" }, { "code": "LB12.Y", "title": "Other specified structural developmental anomalies of oesophagus" }, { "code": "DB99.60", "title": "Cholestasis of parenteral nutrition" }, { "code": "EM0Y", "title": "Other specified diseases of the skin" }, { "code": "KA87.3", "title": "Neonatal hyperbilirubinaemia due to total parenteral nutrition" }, { "code": "PL00", "title": "Drugs, medicaments or biological substances associated with injury or harm in therapeutic use" }, { "code": "5C3Z", "title": "Nutritional disorders, unspecified" } ]
=== ICD-11 CODES FOUND === [DA2Z] Diseases of oesophagus, unspecified Also known as: Diseases of oesophagus, unspecified | disease of oesophagus | disorder of oesophagus | oesophageal disease | oesophageal disorder [DA24.Z] Oesophagitis, unspecified Also known as: Oesophagitis, unspecified | Oesophagitis | inflammation of oesophagus | oesophagitis NOS | oesophageal inflammation [DA20.0] Oesophageal obstruction Definition: Hindrance of the passage of luminal contents in the oesophagus. Obstruction of oesophagus can be partial or complete, and caused by intrinsic or extrinsic factors. Also known as: Oesophageal obstruction | obstruction of oesophagus | oesophageal narrowing | obstructed oesophagus | Stricture of oesophagus Excludes: Congenital stenosis or stricture of oesophagus | Anatomical alteration due to gastro-oesophageal reflux disease | Neoplasms of the oesophagus [DA25.Z] Oesophageal ulcer, unspecified Also known as: Oesophageal ulcer, unspecified | Oesophageal ulcer | Ulcer of oesophagus | ulcer of oesophagus NOS | OU - [oesophageal ulcer] [LB12.Y] Other specified structural developmental anomalies of oesophagus Also known as: Other specified structural developmental anomalies of oesophagus | Absence of oesophagus | Agenesis of oesophagus | Congenital displacement of oesophagus | Duplication of oesophagus [DB99.60] Cholestasis of parenteral nutrition Definition: This is a condition where bile cannot flow from the liver to the duodenum, so one must feed a person intravenously, bypassing the usual process of eating and digestion. Also known as: Cholestasis of parenteral nutrition [EM0Y] Other specified diseases of the skin Also known as: Other specified diseases of the skin | Adverse cutaneous effects of healthcare related interventions | Cutaneous complications of surgical, laser or other interventional procedures | Postprocedural cutaneous complications of surgical, laser or other interventions | Cutaneous complications of surgical procedures [KA87.3] Neonatal hyperbilirubinaemia due to total parenteral nutrition Definition: A paediatric condition characterised by persistently increased level of bilirubin above 85 umol/l (5 mg/dL) manifesting as yellowing of the eyes, skin, and other tissues of a newborn due to intravenous feeding which bypasses the normal processes of eating and digestion. Also known as: Neonatal hyperbilirubinaemia due to total parenteral nutrition [PL00] Drugs, medicaments or biological substances associated with injury or harm in therapeutic use Also known as: Drugs, medicaments or biological substances associated with injury or harm in therapeutic use | Drugs medicaments or biological substances associated with injury or harm in therapeutic use, Systemic antibiotics | Drugs medicaments or biological substances associated with injury or harm in therapeutic use, Systemic antibiotics, Penicillins | Drugs medicaments or biological substances associated with injury or harm in therapeutic use, Systemic antibiotics, Cephalosporins or other beta-lactam antibiotics | Drugs medicaments or biological substances associated with injury or harm in therapeutic use, Systemic antibiotics, Chloramphenicol group Excludes: Circumstances associated with exposure to a drug, medicament or biological substance influencing the episode of care without injury or harm [5C3Z] Nutritional disorders, unspecified Also known as: Nutritional disorders, unspecified | nutritional disease NOS | disorder of nutrition | nutritional disturbance | Nutritional liver disease, not elsewhere classified === GRAPH WALKS === --- Walk 1 --- [DA2Z] Diseases of oesophagus, unspecified --PARENT--> [?] Diseases of oesophagus --RELATED_TO--> [?] Structural developmental anomalies of oesophagus Def: Any congenital defect of oesophagus that results from interference with the normal growth and differentiation of the fetus. Such defects can arise at any stage of embryonic development, vary greatly i... --- Walk 2 --- [DA2Z] Diseases of oesophagus, unspecified --PARENT--> [?] Diseases of oesophagus --RELATED_TO--> [?] Structural developmental anomalies of oesophagus Def: Any congenital defect of oesophagus that results from interference with the normal growth and differentiation of the fetus. Such defects can arise at any stage of embryonic development, vary greatly i... --- Walk 3 --- [DA24.Z] Oesophagitis, unspecified --PARENT--> [DA24] Oesophagitis Def: Oesophagitis is inflammation of the oesophagus. Oesophagitis can cause painful, difficult swallowing and chest pain. Oesophagitis has several causes; some common causes include stomach reflux, infecti... --CHILD--> [DA24.0] Infectious oesophagitis Def: Infectious oesophagitis is inflammation, irritation and swelling of the oesophagus due to the infectious agent.... --- Walk 4 --- [DA24.Z] Oesophagitis, unspecified --PARENT--> [DA24] Oesophagitis Def: Oesophagitis is inflammation of the oesophagus. Oesophagitis can cause painful, difficult swallowing and chest pain. Oesophagitis has several causes; some common causes include stomach reflux, infecti... --CHILD--> [DA24.0] Infectious oesophagitis Def: Infectious oesophagitis is inflammation, irritation and swelling of the oesophagus due to the infectious agent.... --- Walk 5 --- [DA20.0] Oesophageal obstruction Def: Hindrance of the passage of luminal contents in the oesophagus. Obstruction of oesophagus can be partial or complete, and caused by intrinsic or extrinsic factors.... --EXCLUDES--> [?] Congenital stenosis or stricture of oesophagus Def: A form of incomplete oesophageal obstruction due to a developmental defect of the primitive foregut. Abnormal narrowing of the oesophagus occurs most often at the junction of the middle and lower thir... --CHILD--> [?] Congenital stenosis of oesophagus --- Walk 6 --- [DA20.0] Oesophageal obstruction Def: Hindrance of the passage of luminal contents in the oesophagus. Obstruction of oesophagus can be partial or complete, and caused by intrinsic or extrinsic factors.... --EXCLUDES--> [?] Neoplasms of the oesophagus Def: An abnormal tumour that form in tissues lining the oesophagus.... --CHILD--> [?] Malignant neoplasm metastasis in the oesophagus Def: A malignant neoplasm that has spread to the esophagus from another organ or system, or from another primary esophageal tumour. The primary esophageal tumour is not in continuity with the metastatic le...
[ "[DA2Z] Diseases of oesophagus, unspecified\n --PARENT--> [?] Diseases of oesophagus\n --RELATED_TO--> [?] Structural developmental anomalies of oesophagus\n Def: Any congenital defect of oesophagus that results from interference with the normal growth and differentiation of the fetus. Such defects can arise at any stage of embryonic development, vary greatly i...", "[DA2Z] Diseases of oesophagus, unspecified\n --PARENT--> [?] Diseases of oesophagus\n --RELATED_TO--> [?] Structural developmental anomalies of oesophagus\n Def: Any congenital defect of oesophagus that results from interference with the normal growth and differentiation of the fetus. Such defects can arise at any stage of embryonic development, vary greatly i...", "[DA24.Z] Oesophagitis, unspecified\n --PARENT--> [DA24] Oesophagitis\n Def: Oesophagitis is inflammation of the oesophagus. Oesophagitis can cause painful, difficult swallowing and chest pain. Oesophagitis has several causes; some common causes include stomach reflux, infecti...\n --CHILD--> [DA24.0] Infectious oesophagitis\n Def: Infectious oesophagitis is inflammation, irritation and swelling of the oesophagus due to the infectious agent....", "[DA24.Z] Oesophagitis, unspecified\n --PARENT--> [DA24] Oesophagitis\n Def: Oesophagitis is inflammation of the oesophagus. Oesophagitis can cause painful, difficult swallowing and chest pain. Oesophagitis has several causes; some common causes include stomach reflux, infecti...\n --CHILD--> [DA24.0] Infectious oesophagitis\n Def: Infectious oesophagitis is inflammation, irritation and swelling of the oesophagus due to the infectious agent....", "[DA20.0] Oesophageal obstruction\n Def: Hindrance of the passage of luminal contents in the oesophagus. Obstruction of oesophagus can be partial or complete, and caused by intrinsic or extrinsic factors....\n --EXCLUDES--> [?] Congenital stenosis or stricture of oesophagus\n Def: A form of incomplete oesophageal obstruction due to a developmental defect of the primitive foregut. Abnormal narrowing of the oesophagus occurs most often at the junction of the middle and lower thir...\n --CHILD--> [?] Congenital stenosis of oesophagus", "[DA20.0] Oesophageal obstruction\n Def: Hindrance of the passage of luminal contents in the oesophagus. Obstruction of oesophagus can be partial or complete, and caused by intrinsic or extrinsic factors....\n --EXCLUDES--> [?] Neoplasms of the oesophagus\n Def: An abnormal tumour that form in tissues lining the oesophagus....\n --CHILD--> [?] Malignant neoplasm metastasis in the oesophagus\n Def: A malignant neoplasm that has spread to the esophagus from another organ or system, or from another primary esophageal tumour. The primary esophageal tumour is not in continuity with the metastatic le..." ]
DA2Z
Diseases of oesophagus, unspecified
[ { "from_icd11": "DA2Z", "icd10_code": "K228", "icd10_title": "Other specified diseases of esophagus" }, { "from_icd11": "DA2Z", "icd10_code": "K229", "icd10_title": "Disease of esophagus, unspecified" }, { "from_icd11": "DA2Z", "icd10_code": "K22", "icd10_title": "Other diseases of esophagus" }, { "from_icd11": "DA2Z", "icd10_code": "K20-K31", "icd10_title": "" }, { "from_icd11": "DA2Z", "icd10_code": "K23", "icd10_title": "Disorders of esophagus in diseases classified elsewhere" }, { "from_icd11": "DA2Z", "icd10_code": "K238", "icd10_title": "" }, { "from_icd11": "DA24.Z", "icd10_code": "K208", "icd10_title": "Other esophagitis" }, { "from_icd11": "DA24.Z", "icd10_code": "K209", "icd10_title": "Esophagitis, unspecified" }, { "from_icd11": "DA24.Z", "icd10_code": "K200", "icd10_title": "Eosinophilic esophagitis" }, { "from_icd11": "DA24.Z", "icd10_code": "K210", "icd10_title": "Gastro-esophageal reflux disease with esophagitis" }, { "from_icd11": "DA24.Z", "icd10_code": "K20", "icd10_title": "Esophagitis" }, { "from_icd11": "DA20.0", "icd10_code": "K222", "icd10_title": "Esophageal obstruction" }, { "from_icd11": "DA25.Z", "icd10_code": "K2211", "icd10_title": "Ulcer of esophagus with bleeding" }, { "from_icd11": "DA25.Z", "icd10_code": "K2210", "icd10_title": "Ulcer of esophagus without bleeding" }, { "from_icd11": "DA25.Z", "icd10_code": "K221", "icd10_title": "Ulcer of esophagus" } ]
K228
Other specified diseases of esophagus
On day 8, despite being afebrile, he complained of severe generalized abdominal pain. Examination revealed a distended, severely tender abdomen. He was clinically pale. His blood pressure dropped to 80/60. Pulse rate 140 bpm. Investigations—Hb 8.8 g/dl, PCV 26%, WBC 4,000/mm 3 , platelets 90,000/mm 3 . His coagulation profile was normal. A concealed bleed was suspected and the patient was transfused with two pints of packed red cells. An ultrasound scan of the abdomen at that time revealed a large amount of free fluid in the pelvis and Morrison’s pouch. A contrast enhanced computed tomography (CT) scan of the abdomen was performed which revealed free fluid in the peritoneal cavity with a per-splenic haematoma. The patient was taken over to the surgical ward and an emergency laparotomy was performed. There was approximately 4 l of blood in the peritoneal cavity and a 4 cm splenic laceration close to the upper pole . Splenectomy was done. Four pints of packed rec cells were transfused during the surgery. Post Op day 1 the patient was haemodynamically stable. Hb 11.5 g/dl, PCV 35, WBC 14,000/mm 3 , platelets 183,000/mm 3 . The splenic histology was normal. The patient was discharged home 5 days following surgery. Figure 1 Contrast enhanced computed tomography scan of the abdomen—free fluid in peritoneal cavity with splenic laceration. Figure 2 Post-splenectomy—splenic laceration close to upper pole.
3.53125
0.986328
sec[1]/p[1]
en
0.999997
26136216
https://doi.org/10.1186/s13104-015-1234-5
[ "splenic", "abdomen", "scan", "free", "fluid", "peritoneal", "cavity", "laceration", "blood", "platelets" ]
[ { "code": "3B8Z", "title": "Diseases of spleen, unspecified" }, { "code": "LA8Z", "title": "Structural developmental anomaly of heart or great vessels, unspecified" }, { "code": "3B81.Y", "title": "Other specified acquired disorders of spleen" }, { "code": "LB22.Y", "title": "Other specified structural developmental anomalies of spleen" }, { "code": "3B81.2", "title": "Atrophy of spleen" }, { "code": "MD81.3", "title": "Acute abdomen" }, { "code": "JA01.0", "title": "Abdominal pregnancy" }, { "code": "ME04.Z", "title": "Ascites, unspecified" }, { "code": "NB51.0&XA3KX0", "title": "Laceration without foreign body of abdominal wall" }, { "code": "NB9Y", "title": "Other specified injuries to the abdomen, lower back, lumbar spine or pelvis" } ]
=== ICD-11 CODES FOUND === [3B8Z] Diseases of spleen, unspecified Also known as: Diseases of spleen, unspecified | splenic disease | splenopathy [LA8Z] Structural developmental anomaly of heart or great vessels, unspecified Also known as: Structural developmental anomaly of heart or great vessels, unspecified | Heart malformations | Cardiac malformations | congenital anomaly of heart | congenital heart disease [3B81.Y] Other specified acquired disorders of spleen Also known as: Other specified acquired disorders of spleen | Peliosis of spleen | Congestion of spleen | splenic congestion | Lymphoid hyperplasia of spleen [LB22.Y] Other specified structural developmental anomalies of spleen Also known as: Other specified structural developmental anomalies of spleen | Congenital malformation of spleen | malformations of spleen NOS | Aberrant spleen | Congenital lobulation of spleen [3B81.2] Atrophy of spleen Definition: A disease caused by determinants arising after birth, during the antenatal period or by genetically inherited factors. This disease is characterised by partial or complete degradation of the spleen. This disease may present with increased susceptibility to infection. Confirmation is through medical imaging. Also known as: Atrophy of spleen | hyposplenism | splenic atrophy | Hyposplenism due to previous infarction of spleen | Degenerative diseases of the spleen [MD81.3] Acute abdomen Definition: A clinical syndrome with acute abdominal pain that is severe, and rapid onset. Acute abdomen may be caused by a variety of disorders, injuries, or diseases Also known as: Acute abdomen | acute abdominal pain syndrome | surgical abdomen | abdominal acute syndrome | severe abdomen pain [JA01.0] Abdominal pregnancy Definition: A condition characterised by implantation of the embryo within the peritoneal cavity during pregnancy. Also known as: Abdominal pregnancy | abdomen pregnancy | intraperitoneal pregnancy Excludes: Maternal care for viable fetus in abdominal pregnancy | Delivery of viable fetus in abdominal pregnancy [ME04.Z] Ascites, unspecified Also known as: Ascites, unspecified | Ascites | abdominal dropsy | hydrops abdominis | ascites NOS [NB9Y] Other specified injuries to the abdomen, lower back, lumbar spine or pelvis Also known as: Other specified injuries to the abdomen, lower back, lumbar spine or pelvis | Abdominal wall trauma | Injury of pelvic floor | pelvic floor blunt injury | pelvic floor blunt trauma === GRAPH WALKS === --- Walk 1 --- [3B8Z] Diseases of spleen, unspecified --PARENT--> [?] Diseases of spleen --CHILD--> [3B81] Acquired disorders of spleen Def: Any condition caused by determinants acquired after birth, leading to dysfunction of the spleen.... --- Walk 2 --- [3B8Z] Diseases of spleen, unspecified --PARENT--> [?] Diseases of spleen --CHILD--> [3B8Z] Diseases of spleen, unspecified --- Walk 3 --- [LA8Z] Structural developmental anomaly of heart or great vessels, unspecified --PARENT--> [?] Structural developmental anomaly of heart or great vessels Def: A congenital malformation of the heart and/or great vessels or an acquired abnormality unique to the congenitally malformed heart.... --RELATED_TO--> [?] Congenital great vessel related acquired abnormality Def: Any postnatal pathological change in form or function of the heart and/or great vessels consequent to the presence of congenital cardiovascular disease.... --- Walk 4 --- [LA8Z] Structural developmental anomaly of heart or great vessels, unspecified --PARENT--> [?] Structural developmental anomaly of heart or great vessels Def: A congenital malformation of the heart and/or great vessels or an acquired abnormality unique to the congenitally malformed heart.... --RELATED_TO--> [?] Congenital great vessel related acquired abnormality Def: Any postnatal pathological change in form or function of the heart and/or great vessels consequent to the presence of congenital cardiovascular disease.... --- Walk 5 --- [3B81.Y] Other specified acquired disorders of spleen --PARENT--> [3B81] Acquired disorders of spleen Def: Any condition caused by determinants acquired after birth, leading to dysfunction of the spleen.... --CHILD--> [3B81.1] Postsurgical asplenia Def: A disease caused by underlying diseases, splenectomy or splenic rupture from trauma. This disease is characterised by absence of normal spleen function. This disease may present with increased suscept... --- Walk 6 --- [3B81.Y] Other specified acquired disorders of spleen --PARENT--> [3B81] Acquired disorders of spleen Def: Any condition caused by determinants acquired after birth, leading to dysfunction of the spleen.... --RELATED_TO--> [?] Malignant neoplasms of the spleen
[ "[3B8Z] Diseases of spleen, unspecified\n --PARENT--> [?] Diseases of spleen\n --CHILD--> [3B81] Acquired disorders of spleen\n Def: Any condition caused by determinants acquired after birth, leading to dysfunction of the spleen....", "[3B8Z] Diseases of spleen, unspecified\n --PARENT--> [?] Diseases of spleen\n --CHILD--> [3B8Z] Diseases of spleen, unspecified", "[LA8Z] Structural developmental anomaly of heart or great vessels, unspecified\n --PARENT--> [?] Structural developmental anomaly of heart or great vessels\n Def: A congenital malformation of the heart and/or great vessels or an acquired abnormality unique to the congenitally malformed heart....\n --RELATED_TO--> [?] Congenital great vessel related acquired abnormality\n Def: Any postnatal pathological change in form or function of the heart and/or great vessels consequent to the presence of congenital cardiovascular disease....", "[LA8Z] Structural developmental anomaly of heart or great vessels, unspecified\n --PARENT--> [?] Structural developmental anomaly of heart or great vessels\n Def: A congenital malformation of the heart and/or great vessels or an acquired abnormality unique to the congenitally malformed heart....\n --RELATED_TO--> [?] Congenital great vessel related acquired abnormality\n Def: Any postnatal pathological change in form or function of the heart and/or great vessels consequent to the presence of congenital cardiovascular disease....", "[3B81.Y] Other specified acquired disorders of spleen\n --PARENT--> [3B81] Acquired disorders of spleen\n Def: Any condition caused by determinants acquired after birth, leading to dysfunction of the spleen....\n --CHILD--> [3B81.1] Postsurgical asplenia\n Def: A disease caused by underlying diseases, splenectomy or splenic rupture from trauma. This disease is characterised by absence of normal spleen function. This disease may present with increased suscept...", "[3B81.Y] Other specified acquired disorders of spleen\n --PARENT--> [3B81] Acquired disorders of spleen\n Def: Any condition caused by determinants acquired after birth, leading to dysfunction of the spleen....\n --RELATED_TO--> [?] Malignant neoplasms of the spleen" ]
3B8Z
Diseases of spleen, unspecified
[ { "from_icd11": "3B8Z", "icd10_code": "D7389", "icd10_title": "Other diseases of spleen" }, { "from_icd11": "3B8Z", "icd10_code": "D7381", "icd10_title": "Neutropenic splenomegaly" }, { "from_icd11": "3B8Z", "icd10_code": "D739", "icd10_title": "Disease of spleen, unspecified" }, { "from_icd11": "3B8Z", "icd10_code": "D73", "icd10_title": "Diseases of spleen" }, { "from_icd11": "3B8Z", "icd10_code": "D738", "icd10_title": "Other diseases of spleen" }, { "from_icd11": "LA8Z", "icd10_code": "Q248", "icd10_title": "Other specified congenital malformations of heart" }, { "from_icd11": "LA8Z", "icd10_code": "Q893", "icd10_title": "Situs inversus" }, { "from_icd11": "LA8Z", "icd10_code": "Q212", "icd10_title": "Atrioventricular septal defect" }, { "from_icd11": "LA8Z", "icd10_code": "Q249", "icd10_title": "Congenital malformation of heart, unspecified" }, { "from_icd11": "LA8Z", "icd10_code": "Q246", "icd10_title": "Congenital heart block" }, { "from_icd11": "LA8Z", "icd10_code": "Q242", "icd10_title": "Cor triatriatum" }, { "from_icd11": "LA8Z", "icd10_code": "Q219", "icd10_title": "Congenital malformation of cardiac septum, unspecified" }, { "from_icd11": "LA8Z", "icd10_code": "Q208", "icd10_title": "Other congenital malformations of cardiac chambers and connections" }, { "from_icd11": "LA8Z", "icd10_code": "Q897", "icd10_title": "Multiple congenital malformations, not elsewhere classified" }, { "from_icd11": "LA8Z", "icd10_code": "Q209", "icd10_title": "Congenital malformation of cardiac chambers and connections, unspecified" } ]
D7389
Other diseases of spleen
Systemic chemotherapy was started in January 2021 with an initial dose of albumin-bound paclitaxel 400 mg and carboplatin 0.4 mg. Rash and pruritus developed during the second chemotherapy infusion of carboplatin, so treatment with carboplatin was discontinued. After 2 cycles of chemotherapy, objective tumor remission was evaluated as disease stabilization (SD) by RECIST 1.1 (efficacy evaluation criteria for solid tumors). After nearly 8 weeks of oral administration of the third-generation EGFR-TKI aumolertinib (110 mg/day) started in February 2021, imaging showed significant tumor regression, lesion volume reduction to 2.2 × 2.0 × 1.8 cm, partial remission (PR), and clinical stage reduction to stage IB (T2N0M0). After evaluation by the surgeon, the patient was eligible for surgery and underwent VATS left upper lung lobectomy + lymph node dissection with the patient’s consent in April 2021. Postoperative pathology showed interstitial fibrous lung tissue with numerous lymphocytic infiltrates, with large necrotic tissue and <10% residual tumor cells (major pathological response, MPR), which was considered as posttreatment changes of squamous carcinoma. There was no metastasis of cancer tissue in any of the lymph nodes examined. After discussion with the patient, he was willing to receive adjuvant therapy with aumolertinib, and the disease was judged to be stable by imaging results in February 2022.
3.966797
0.955078
sec[1]/sec[0]/p[1]
en
0.999995
PMC9004604
https://doi.org/10.3389/fonc.2022.872225
[ "chemotherapy", "carboplatin", "tumor", "tissue", "remission", "aumolertinib", "february", "imaging", "reduction", "stage" ]
[ { "code": "QB97", "title": "Contact with health services for chemotherapy session for neoplasm" }, { "code": "QC05.Y", "title": "Other specified prophylactic measures" }, { "code": "QB9Y", "title": "Other specified contact with health services for nonsurgical interventions not involving devices" }, { "code": "3B64.1Y", "title": "Other specified acquired thrombocytopenia" }, { "code": "QC48.Y", "title": "Other specified personal history of medical treatment" }, { "code": "2F9Z", "title": "Neoplasms of unknown behaviour of unspecified site" }, { "code": "ME61", "title": "Subcutaneous swelling, mass or lump of uncertain or unspecified nature" }, { "code": "2E6Z", "title": "Carcinoma in situ of unspecified site" }, { "code": "2F91.1", "title": "Neoplasms of unknown behaviour of trachea, bronchus or lung" }, { "code": "2F92", "title": "Neoplasms of unknown behaviour of skin" } ]
=== ICD-11 CODES FOUND === [QB97] Contact with health services for chemotherapy session for neoplasm Also known as: Contact with health services for chemotherapy session for neoplasm | antineoplastic chemotherapy regimen | cancer chemotherapy regimen | maintenance chemotherapy for neoplasm | neoplasm chemotherapy [QC05.Y] Other specified prophylactic measures Also known as: Other specified prophylactic measures | Other prophylactic chemotherapy | chemoprophylaxis | prophylactic chemotherapy | Systemic prophylactic chemotherapy [QB9Y] Other specified contact with health services for nonsurgical interventions not involving devices Also known as: Other specified contact with health services for nonsurgical interventions not involving devices | Chemotherapy other than for neoplasm | admission for chemotherapy administration other than for neoplasm | chemotherapy regimen other than for neoplasm | drug therapy other than for neoplasm [3B64.1Y] Other specified acquired thrombocytopenia Also known as: Other specified acquired thrombocytopenia | Acquired thrombocytopenia specified as refractory | Chemotherapy thrombocytopaenia | Liver thrombocytopaenia [QC48.Y] Other specified personal history of medical treatment Also known as: Other specified personal history of medical treatment | Personal history of contraception | history of contraception | Personal history of long-term use of medicaments other than anticoagulants | personal history of long term current use of medicaments [2F9Z] Neoplasms of unknown behaviour of unspecified site Also known as: Neoplasms of unknown behaviour of unspecified site | neoplasia | neoplasm growth NOS | tumour of unspecified site | tumourlet of unspecified site [ME61] Subcutaneous swelling, mass or lump of uncertain or unspecified nature Definition: One or more localised subcutaneous soft tissue masses of undetermined or unspecified nature Also known as: Subcutaneous swelling, mass or lump of uncertain or unspecified nature | localised swelling, mass or lump of skin and subcutaneous tissue | localised subcutaneous nodules | subcutaneous nodules | superficial subcutaneous nodules Excludes: localized adiposity | mass and lump: breast | enlarged lymph nodes [2E6Z] Carcinoma in situ of unspecified site Also known as: Carcinoma in situ of unspecified site | carcinoma in situ of unspecified site | carcinoma in situ NOS | carcinoma in situ | in situ neoplasm [2F91.1] Neoplasms of unknown behaviour of trachea, bronchus or lung Also known as: Neoplasms of unknown behaviour of trachea, bronchus or lung | trachea, bronchus or lung tumour NOS | Intravascular bronchial alveolar tumour of unspecified site | Bronchial adenoma of unknown behaviour of unspecified site | Intravascular bronchial alveolar tumour unknown behaviour of unspecified site [2F92] Neoplasms of unknown behaviour of skin Also known as: Neoplasms of unknown behaviour of skin | skin tumour NOS === GRAPH WALKS === --- Walk 1 --- [QB97] Contact with health services for chemotherapy session for neoplasm --PARENT--> [?] Contact with health services for nonsurgical interventions not involving devices --PARENT--> [?] Reasons for contact with the health services --- Walk 2 --- [QB97] Contact with health services for chemotherapy session for neoplasm --PARENT--> [?] Contact with health services for nonsurgical interventions not involving devices --CHILD--> [QB91] Contact with health services for piercing of body site other than ear --- Walk 3 --- [QC05.Y] Other specified prophylactic measures --PARENT--> [QC05] Need for certain specified other prophylactic measures --CHILD--> [QC05.Y] Other specified prophylactic measures --- Walk 4 --- [QC05.Y] Other specified prophylactic measures --PARENT--> [QC05] Need for certain specified other prophylactic measures --EXCLUDES--> [?] Allergen immunotherapy Def: Allergen immunotherapy (AIT) is the stimulation of the immune system with the administration of gradually increasing doses of the substance/allergen to which the patient is allergic. AIT is indicated ... --- Walk 5 --- [QB9Y] Other specified contact with health services for nonsurgical interventions not involving devices --PARENT--> [?] Contact with health services for nonsurgical interventions not involving devices --PARENT--> [?] Reasons for contact with the health services --- Walk 6 --- [QB9Y] Other specified contact with health services for nonsurgical interventions not involving devices --PARENT--> [?] Contact with health services for nonsurgical interventions not involving devices --CHILD--> [QB91] Contact with health services for piercing of body site other than ear
[ "[QB97] Contact with health services for chemotherapy session for neoplasm\n --PARENT--> [?] Contact with health services for nonsurgical interventions not involving devices\n --PARENT--> [?] Reasons for contact with the health services", "[QB97] Contact with health services for chemotherapy session for neoplasm\n --PARENT--> [?] Contact with health services for nonsurgical interventions not involving devices\n --CHILD--> [QB91] Contact with health services for piercing of body site other than ear", "[QC05.Y] Other specified prophylactic measures\n --PARENT--> [QC05] Need for certain specified other prophylactic measures\n --CHILD--> [QC05.Y] Other specified prophylactic measures", "[QC05.Y] Other specified prophylactic measures\n --PARENT--> [QC05] Need for certain specified other prophylactic measures\n --EXCLUDES--> [?] Allergen immunotherapy\n Def: Allergen immunotherapy (AIT) is the stimulation of the immune system with the administration of gradually increasing doses of the substance/allergen to which the patient is allergic. AIT is indicated ...", "[QB9Y] Other specified contact with health services for nonsurgical interventions not involving devices\n --PARENT--> [?] Contact with health services for nonsurgical interventions not involving devices\n --PARENT--> [?] Reasons for contact with the health services", "[QB9Y] Other specified contact with health services for nonsurgical interventions not involving devices\n --PARENT--> [?] Contact with health services for nonsurgical interventions not involving devices\n --CHILD--> [QB91] Contact with health services for piercing of body site other than ear" ]
QB97
Contact with health services for chemotherapy session for neoplasm
[ { "from_icd11": "QB97", "icd10_code": "Z5111", "icd10_title": "Encounter for antineoplastic chemotherapy" }, { "from_icd11": "QB97", "icd10_code": "Z5112", "icd10_title": "Encounter for antineoplastic immunotherapy" }, { "from_icd11": "QB97", "icd10_code": "Z511", "icd10_title": "Encounter for antineoplastic chemotherapy and immunotherapy" }, { "from_icd11": "QB97", "icd10_code": "Z51", "icd10_title": "Encounter for other aftercare and medical care" }, { "from_icd11": "QB9Y", "icd10_code": "Z5181", "icd10_title": "Encounter for therapeutic drug level monitoring" }, { "from_icd11": "QC48.Y", "icd10_code": "Z794", "icd10_title": "Long term (current) use of insulin" }, { "from_icd11": "QC48.Y", "icd10_code": "Z7902", "icd10_title": "Long term (current) use of antithrombotics/antiplatelets" }, { "from_icd11": "QC48.Y", "icd10_code": "Z7982", "icd10_title": "Long term (current) use of aspirin" }, { "from_icd11": "QC48.Y", "icd10_code": "Z7984", "icd10_title": "Long term (current) use of oral hypoglycemic drugs" }, { "from_icd11": "QC48.Y", "icd10_code": "Z79899", "icd10_title": "Other long term (current) drug therapy" }, { "from_icd11": "2F9Z", "icd10_code": "D487", "icd10_title": "Neoplasm of uncertain behavior of other specified sites" }, { "from_icd11": "2F9Z", "icd10_code": "D482", "icd10_title": "Neoplasm of uncertain behavior of peripheral nerves and autonomic nervous system" }, { "from_icd11": "2F9Z", "icd10_code": "D37-D48", "icd10_title": "" }, { "from_icd11": "2F9Z", "icd10_code": "D377", "icd10_title": "" }, { "from_icd11": "2F9Z", "icd10_code": "D48", "icd10_title": "Neoplasm of uncertain behavior of other and unspecified sites" } ]
Z5111
Encounter for antineoplastic chemotherapy
After these episodes she was transferred to our metabolic unit for further investigation. In her basal state, she persistently maintained mildly elevated lactate plasma levels (2.3–2.5 mmol/L); urine gas chromatography showed increased excretion of ketone bodies , lactate, 2-hydroxy butyrate and 3-hydroxy isovalerate, all compatible with an underlying mitochondrial disorder (see Table 1 ). Slight elevation of plasma alanine (Ala) was detected in one determination, but it was not sustained (see Table 1 ). Lactate and amino acids levels in cerebrospinal fluid were normal in basal state [lactate: 1.67 mM, Ala: 30 μmol/L (NV: 30 ± 11)]. Table 1 Metabolic study at different times in the patient's life and after 18 h of fasting Age 7 Months (no acidosis) 10 Months (no acidosis) 15 Months (no acidosis) 15 Months, 18 h of fasting Urine organic acids (mmol/mol creatinine) 3-Hydroxy butyrate (NV: 2–17) 158 1114 284 15,471 Acetoacetate (NV: 0–7) 117 792 20 9342 Lactate (NV: 5–113) 9312 359 28 23,846 2-Hydroxy butyrate(NV: 0–4) 380 273 15 11,944 3-Hydroxy isovalerate (NV: 1–40) 56 56 19 315 Plasma amino acids (μmol/L) Alanine (NV: 297 ± 96) 435 230 329 124 Others Normal Normal Normal Elevation of BCAA due to severe ketosis Plasma acylcarnitines μmol/L Normal Normal Normal Mild elevation of C12–C14 due to ketosis NV normal value, C12 dodecanoylcarnitine, C14 myristoylcarnitine, BCAA branched-chain amino acids
4.171875
0.797363
sec[2]/sec[0]/p[1]
en
0.999998
PMC9215049
https://doi.org/10.1186/s13023-022-02389-4
[ "lactate", "hydroxy", "plasma", "acids", "butyrate", "elevation", "amino", "acidosis", "metabolic", "basal" ]
[ { "code": "JB46.3", "title": "Agalactia" }, { "code": "MF31", "title": "Breast or lactation symptom or complaint" }, { "code": "JB46.4", "title": "Hypogalactia" }, { "code": "JB46.6", "title": "Galactorrhoea" }, { "code": "JB46.7", "title": "Other or unspecified disorders of lactation" }, { "code": "5C50.4", "title": "Disorders of lysine or hydroxylysine metabolism" }, { "code": "FA26.1", "title": "Hydroxyapatite deposition disease" }, { "code": "5C50.8", "title": "Disorders of proline or hydroxyproline metabolism" }, { "code": "5C50.E1", "title": "Cerebral organic aciduria" }, { "code": "5C50.E0", "title": "Classical organic aciduria" } ]
=== ICD-11 CODES FOUND === [JB46.3] Agalactia Also known as: Agalactia | Failure of lactation | absence of lactation | not producing any milk | Primary agalactia Includes: Failure of lactation | Primary agalactia [MF31] Breast or lactation symptom or complaint Also known as: Breast or lactation symptom or complaint | lactation problem [JB46.4] Hypogalactia Also known as: Hypogalactia | decreased lactation | hypolactation | inadequate lactation | poor lactation Includes: Insufficient milk supply | Delayed milk supply [JB46.6] Galactorrhoea Definition: Excessive or inappropriate lactation in females or males, and not necessarily related to pregnancy. Galactorrhoea can occur either unilaterally or bilaterally, and be profuse or sparse. Its most common cause is hyperprolactinemia. Also known as: Galactorrhoea | galactorrhoea associated with childbirth | galactorrhoea in pregnancy and the puerperium | increased postpartum lactation | persistent secretion of milk associated with childbirth Includes: Oversupply of milk Excludes: Galactorrhoea not associated with childbirth [JB46.7] Other or unspecified disorders of lactation Also known as: Other or unspecified disorders of lactation | unspecified disorder of lactation, unspecified as to episode of care | puerperal lactation disorder | Other or unspecified disorders of lactation, without mention of attachment difficulty | Other or unspecified disorders of lactation, with mention of attachment difficulty [5C50.4] Disorders of lysine or hydroxylysine metabolism Also known as: Disorders of lysine or hydroxylysine metabolism | glutaric aciduria NOS | Hyperlysinaemia | Lysine alpha-ketoglutarate reductase deficiency | Alpha-aminoadipic semialdehyde deficiency Excludes: Refsum disease | Zellweger syndrome | Glutaryl-CoA dehydrogenase deficiency [FA26.1] Hydroxyapatite deposition disease Definition: Calcium hydroxyapatite crystal deposition disease is characterised by the presence of basic calcium phosphate crystals - predominantly hydroxyapatite - in periarticular soft tissues, especially tendons. This entity is best recognised as "calcific tendinitis" at its most frequent site about the shoulder, but the disease involves numerous other sites and may be more appropriately termed calcific periarthritis. Also known as: Hydroxyapatite deposition disease | apatite-associated destructive arthritis | basic calcium phosphate arthritis | hydroxyapatite deposition disease, unspecified site | idiopathic destructive arthritis [5C50.8] Disorders of proline or hydroxyproline metabolism Also known as: Disorders of proline or hydroxyproline metabolism | Hyperhydroxyprolinaemia | Hydroxyprolinaemia | Hyperprolinaemia type 1 | Proline oxydase deficiency [5C50.E1] Cerebral organic aciduria Definition: This is a term used to classify a group of metabolic disorders which disrupt normal amino acid metabolism, particularly branched-chain amino acids, causing a buildup of acids which are usually not present. Also known as: Cerebral organic aciduria | Glutaric aciduria type 1 | Glutaric acidaemia type 1 | Glutaryl-CoA dehydrogenase deficiency | 2-hydroxyglutaric aciduria [5C50.E0] Classical organic aciduria Definition: This a term used to classify a group of metabolic disorders which disrupt normal amino acid metabolism, particularly branched-chain amino acids, causing a buildup of acids which are usually not present. Also known as: Classical organic aciduria | Methylmalonic aciduria - homocystinuria | Methylmalonic acidaemia - homocystinuria | Methylmalonic aciduria - homocystinuria type cbl C | Methylmalonic acidaemia - homocystinuria type cbl C === GRAPH WALKS === --- Walk 1 --- [JB46.3] Agalactia --PARENT--> [JB46] Certain specified disorders of breast or lactation associated with childbirth --CHILD--> [JB46.0] Retracted nipple associated with childbirth Def: A condition characterised as the abnormal inversion of a nipple that does not return to normal position even when stimulated that has occurred in association with childbirth.... --- Walk 2 --- [JB46.3] Agalactia --PARENT--> [JB46] Certain specified disorders of breast or lactation associated with childbirth --RELATED_TO--> [?] Breast or lactation symptom or complaint --- Walk 3 --- [MF31] Breast or lactation symptom or complaint --PARENT--> [?] Symptoms, signs or clinical findings involving the female genital system --CHILD--> [MF32] Menopausal symptom or complaint --- Walk 4 --- [MF31] Breast or lactation symptom or complaint --PARENT--> [?] Symptoms, signs or clinical findings involving the female genital system --RELATED_TO--> [?] Fear of complications of pregnancy --- Walk 5 --- [JB46.4] Hypogalactia --PARENT--> [JB46] Certain specified disorders of breast or lactation associated with childbirth --CHILD--> [JB46.2] Other or unspecified disorders of breast associated with childbirth --- Walk 6 --- [JB46.4] Hypogalactia --PARENT--> [JB46] Certain specified disorders of breast or lactation associated with childbirth --RELATED_TO--> [?] Breast or lactation symptom or complaint
[ "[JB46.3] Agalactia\n --PARENT--> [JB46] Certain specified disorders of breast or lactation associated with childbirth\n --CHILD--> [JB46.0] Retracted nipple associated with childbirth\n Def: A condition characterised as the abnormal inversion of a nipple that does not return to normal position even when stimulated that has occurred in association with childbirth....", "[JB46.3] Agalactia\n --PARENT--> [JB46] Certain specified disorders of breast or lactation associated with childbirth\n --RELATED_TO--> [?] Breast or lactation symptom or complaint", "[MF31] Breast or lactation symptom or complaint\n --PARENT--> [?] Symptoms, signs or clinical findings involving the female genital system\n --CHILD--> [MF32] Menopausal symptom or complaint", "[MF31] Breast or lactation symptom or complaint\n --PARENT--> [?] Symptoms, signs or clinical findings involving the female genital system\n --RELATED_TO--> [?] Fear of complications of pregnancy", "[JB46.4] Hypogalactia\n --PARENT--> [JB46] Certain specified disorders of breast or lactation associated with childbirth\n --CHILD--> [JB46.2] Other or unspecified disorders of breast associated with childbirth", "[JB46.4] Hypogalactia\n --PARENT--> [JB46] Certain specified disorders of breast or lactation associated with childbirth\n --RELATED_TO--> [?] Breast or lactation symptom or complaint" ]
JB46.3
Agalactia
[ { "from_icd11": "JB46.3", "icd10_code": "O923", "icd10_title": "Agalactia" }, { "from_icd11": "MF31", "icd10_code": "Z0489", "icd10_title": "Encounter for examination and observation for other specified reasons" }, { "from_icd11": "MF31", "icd10_code": "Z048", "icd10_title": "Encounter for examination and observation for other specified reasons" }, { "from_icd11": "JB46.4", "icd10_code": "O924", "icd10_title": "Hypogalactia" }, { "from_icd11": "JB46.6", "icd10_code": "O926", "icd10_title": "Galactorrhea" }, { "from_icd11": "JB46.7", "icd10_code": "O9279", "icd10_title": "Other disorders of lactation" }, { "from_icd11": "JB46.7", "icd10_code": "O927", "icd10_title": "Other and unspecified disorders of lactation" }, { "from_icd11": "JB46.7", "icd10_code": "O9270", "icd10_title": "Unspecified disorders of lactation" }, { "from_icd11": "5C50.4", "icd10_code": "E723", "icd10_title": "Disorders of lysine and hydroxylysine metabolism" }, { "from_icd11": "FA26.1", "icd10_code": "M1100", "icd10_title": "Hydroxyapatite deposition disease, unspecified site" }, { "from_icd11": "FA26.1", "icd10_code": "M110", "icd10_title": "Hydroxyapatite deposition disease" }, { "from_icd11": "5C50.8", "icd10_code": "E7281", "icd10_title": "Disorders of gamma aminobutyric acid metabolism" }, { "from_icd11": "5C50.8", "icd10_code": "E728", "icd10_title": "Other specified disorders of amino-acid metabolism" } ]
O923
Agalactia
In all published case reports, implants were surgically explanted. Sikder and co-authors emphasise the importance of minimising intraoperative trauma to the iris, lens and corneal endothelium. They describe a surgical technique for NewColorIris® implant removal that involves cutting the implant into three equal segments and removing each through a 2.75 mm temporal clear corneal incision . Despite careful explantation, the damage induced by artificial iris anterior chamber implants can be permanent. Our patient developed secondary corneal endothelial cell loss, glaucoma and cataracts as a result of NewColorIris® implants, as well as pressure-induced stromal keratopathy (PISK) . The latter complication has not been described previously in this context and to the best of our knowledge is unique in our patient. PISK is a rare condition affecting eyes that have undergone lamellar corneal refractive surgery . In this case, the patient underwent LASIK one year prior to NewColorIris® implantation and PISK occurred secondary to endothelial cell failure and high IOP. An important consideration is the purported underestimation of IOP by applanation tonometry in the prescence of interface fluid . A complete resolution of interface fluid was observed in both eyes following topical IOP-lowering treatment, iris implant removal and subsequent combined phacoemulsification with intraocular lens insertion and DSEK.
4.148438
0.748047
sec[2]/p[3]
en
0.999997
26253540
https://doi.org/10.1186/s12886-015-0084-1
[ "corneal", "implants", "iris", "newcoloriris", "implant", "pisk", "lens", "removal", "that", "induced" ]
[ { "code": "9A7Z", "title": "Disorders of the cornea, unspecified" }, { "code": "9A71", "title": "Infectious keratitis" }, { "code": "9A76", "title": "Corneal ulcer" }, { "code": "9A78.4", "title": "Corneal degeneration" }, { "code": "9A70.Z", "title": "Hereditary corneal dystrophies, unspecified" }, { "code": "GC7A", "title": "Disorders of breast augmentation" }, { "code": "QB51.7", "title": "Presence of orthopaedic joint implants" }, { "code": "QB51.Y", "title": "Presence of other specified devices other than cardiac or vascular implants" }, { "code": "QB51.5", "title": "Presence of endocrine implants" }, { "code": "QB51.6", "title": "Presence of tooth-root or mandibular implants" } ]
=== ICD-11 CODES FOUND === [9A7Z] Disorders of the cornea, unspecified Also known as: Disorders of the cornea, unspecified | corneal disease | disease of cornea | keratopathy [9A71] Infectious keratitis Also known as: Infectious keratitis | corneal inflammation | Bacterial keratitis | Fungal keratitis | fungal infection of cornea [9A76] Corneal ulcer Definition: Loss of epithelial tissue from the surface of the cornea due to progressive erosion and necrosis of the tissue. It is often caused by bacterial, fungal, or viral infection. Also known as: Corneal ulcer | cornea ulcer | ulcerative keratitis | corneal ulcer NOS | Central corneal ulcer Includes: Central corneal ulcer | Ring corneal ulcer | Corneal ulcer with hypopyon [9A78.4] Corneal degeneration Also known as: Corneal degeneration | degenerative corneal opacity | Pellucid marginal degeneration | Arcus senilis | gerontoxon Includes: Arcus senilis Excludes: Mooren ulcer [9A70.Z] Hereditary corneal dystrophies, unspecified Also known as: Hereditary corneal dystrophies, unspecified | Hereditary corneal dystrophies | hereditary corneal dystrophy | corneal dystrophy NOS | familial hereditary corneal degeneration [GC7A] Disorders of breast augmentation Definition: A group of disorders that may arise in concert with or subsequent to the surgical placement of breast implants. Also known as: Disorders of breast augmentation | Capsule contraction or scarring | Implant rupture [QB51.7] Presence of orthopaedic joint implants Also known as: Presence of orthopaedic joint implants | presence of joint implant | replacement of joint by artificial or mechanical device or prosthesis | Presence of shoulder-joint implant | presence of shoulder joint replacment prosthesis [QB51.Y] Presence of other specified devices other than cardiac or vascular implants Also known as: Presence of other specified devices other than cardiac or vascular implants | Presence of bone or tendon implants other than orthopaedic joint implants | replacement of tendon by artificial or mechanical device or prosthesis | presence of tendon implant | Presence of skull plate [QB51.5] Presence of endocrine implants Also known as: Presence of endocrine implants | presence of insulin pump Includes: presence of insulin pump [QB51.6] Presence of tooth-root or mandibular implants Also known as: Presence of tooth-root or mandibular implants | presence of tooth root implant | presence of mandibular implant === GRAPH WALKS === --- Walk 1 --- [9A7Z] Disorders of the cornea, unspecified --PARENT--> [?] Disorders of the cornea Def: This refers to disorders of the transparent front part of the eye that covers the iris, pupil, and anterior chamber. The cornea, with the anterior chamber and lens, refracts light, with the cornea acc... --CHILD--> [9A71] Infectious keratitis --- Walk 2 --- [9A7Z] Disorders of the cornea, unspecified --PARENT--> [?] Disorders of the cornea Def: This refers to disorders of the transparent front part of the eye that covers the iris, pupil, and anterior chamber. The cornea, with the anterior chamber and lens, refracts light, with the cornea acc... --CHILD--> [9A71] Infectious keratitis --- Walk 3 --- [9A71] Infectious keratitis --RELATED_TO--> [?] Herpes simplex keratitis Def: This is a viral disease from the herpesviridae family caused by both Herpes simplex virus type 1 (HSV-1) and type 2 (HSV-2). Infection with the herpes virus is categorized into one of several distinct... --PARENT--> [?] Viral keratitis Def: This is a parasitic condition in which the eye's cornea, the front part of the eye, becomes inflamed. The condition is often marked by moderate to intense pain and usually involves impaired eyesight. ... --- Walk 4 --- [9A71] Infectious keratitis --RELATED_TO--> [?] Herpes simplex keratitis Def: This is a viral disease from the herpesviridae family caused by both Herpes simplex virus type 1 (HSV-1) and type 2 (HSV-2). Infection with the herpes virus is categorized into one of several distinct... --CHILD--> [?] Neurotrophic keratopathy --- Walk 5 --- [9A76] Corneal ulcer Def: Loss of epithelial tissue from the surface of the cornea due to progressive erosion and necrosis of the tissue. It is often caused by bacterial, fungal, or viral infection.... --PARENT--> [?] Disorders of the cornea Def: This refers to disorders of the transparent front part of the eye that covers the iris, pupil, and anterior chamber. The cornea, with the anterior chamber and lens, refracts light, with the cornea acc... --CHILD--> [9A72] Traumatic keratitis --- Walk 6 --- [9A76] Corneal ulcer Def: Loss of epithelial tissue from the surface of the cornea due to progressive erosion and necrosis of the tissue. It is often caused by bacterial, fungal, or viral infection.... --PARENT--> [?] Disorders of the cornea Def: This refers to disorders of the transparent front part of the eye that covers the iris, pupil, and anterior chamber. The cornea, with the anterior chamber and lens, refracts light, with the cornea acc... --CHILD--> [9A70] Hereditary corneal dystrophies Def: The term corneal dystrophy embraces a heterogeneous group of bilateral genetically determined non-inflammatory corneal diseases that are usually restricted to the cornea. The designation is imprecise ...
[ "[9A7Z] Disorders of the cornea, unspecified\n --PARENT--> [?] Disorders of the cornea\n Def: This refers to disorders of the transparent front part of the eye that covers the iris, pupil, and anterior chamber. The cornea, with the anterior chamber and lens, refracts light, with the cornea acc...\n --CHILD--> [9A71] Infectious keratitis", "[9A7Z] Disorders of the cornea, unspecified\n --PARENT--> [?] Disorders of the cornea\n Def: This refers to disorders of the transparent front part of the eye that covers the iris, pupil, and anterior chamber. The cornea, with the anterior chamber and lens, refracts light, with the cornea acc...\n --CHILD--> [9A71] Infectious keratitis", "[9A71] Infectious keratitis\n --RELATED_TO--> [?] Herpes simplex keratitis\n Def: This is a viral disease from the herpesviridae family caused by both Herpes simplex virus type 1 (HSV-1) and type 2 (HSV-2). Infection with the herpes virus is categorized into one of several distinct...\n --PARENT--> [?] Viral keratitis\n Def: This is a parasitic condition in which the eye's cornea, the front part of the eye, becomes inflamed. The condition is often marked by moderate to intense pain and usually involves impaired eyesight. ...", "[9A71] Infectious keratitis\n --RELATED_TO--> [?] Herpes simplex keratitis\n Def: This is a viral disease from the herpesviridae family caused by both Herpes simplex virus type 1 (HSV-1) and type 2 (HSV-2). Infection with the herpes virus is categorized into one of several distinct...\n --CHILD--> [?] Neurotrophic keratopathy", "[9A76] Corneal ulcer\n Def: Loss of epithelial tissue from the surface of the cornea due to progressive erosion and necrosis of the tissue. It is often caused by bacterial, fungal, or viral infection....\n --PARENT--> [?] Disorders of the cornea\n Def: This refers to disorders of the transparent front part of the eye that covers the iris, pupil, and anterior chamber. The cornea, with the anterior chamber and lens, refracts light, with the cornea acc...\n --CHILD--> [9A72] Traumatic keratitis", "[9A76] Corneal ulcer\n Def: Loss of epithelial tissue from the surface of the cornea due to progressive erosion and necrosis of the tissue. It is often caused by bacterial, fungal, or viral infection....\n --PARENT--> [?] Disorders of the cornea\n Def: This refers to disorders of the transparent front part of the eye that covers the iris, pupil, and anterior chamber. The cornea, with the anterior chamber and lens, refracts light, with the cornea acc...\n --CHILD--> [9A70] Hereditary corneal dystrophies\n Def: The term corneal dystrophy embraces a heterogeneous group of bilateral genetically determined non-inflammatory corneal diseases that are usually restricted to the cornea. The designation is imprecise ..." ]
9A7Z
Disorders of the cornea, unspecified
[ { "from_icd11": "9A7Z", "icd10_code": "H16203", "icd10_title": "Unspecified keratoconjunctivitis, bilateral" }, { "from_icd11": "9A7Z", "icd10_code": "H16229", "icd10_title": "Keratoconjunctivitis sicca, not specified as Sjogren's, unspecified eye" }, { "from_icd11": "9A7Z", "icd10_code": "H16231", "icd10_title": "Neurotrophic keratoconjunctivitis, right eye" }, { "from_icd11": "9A7Z", "icd10_code": "H16213", "icd10_title": "Exposure keratoconjunctivitis, bilateral" }, { "from_icd11": "9A7Z", "icd10_code": "H16209", "icd10_title": "Unspecified keratoconjunctivitis, unspecified eye" }, { "from_icd11": "9A7Z", "icd10_code": "H16221", "icd10_title": "Keratoconjunctivitis sicca, not specified as Sjogren's, right eye" }, { "from_icd11": "9A7Z", "icd10_code": "H16222", "icd10_title": "Keratoconjunctivitis sicca, not specified as Sjogren's, left eye" }, { "from_icd11": "9A7Z", "icd10_code": "H16202", "icd10_title": "Unspecified keratoconjunctivitis, left eye" }, { "from_icd11": "9A7Z", "icd10_code": "H16299", "icd10_title": "Other keratoconjunctivitis, unspecified eye" }, { "from_icd11": "9A7Z", "icd10_code": "H16292", "icd10_title": "Other keratoconjunctivitis, left eye" }, { "from_icd11": "9A7Z", "icd10_code": "H16219", "icd10_title": "Exposure keratoconjunctivitis, unspecified eye" }, { "from_icd11": "9A7Z", "icd10_code": "H169", "icd10_title": "Unspecified keratitis" }, { "from_icd11": "9A7Z", "icd10_code": "H189", "icd10_title": "Unspecified disorder of cornea" }, { "from_icd11": "9A7Z", "icd10_code": "H168", "icd10_title": "Other keratitis" }, { "from_icd11": "9A7Z", "icd10_code": "H162", "icd10_title": "Keratoconjunctivitis" } ]
H16203
Unspecified keratoconjunctivitis, bilateral
A 23-year old female was referred because of hemoptysis. She had had aortic coarctation repair with a prosthetic patch at the age of 6. Eight years later an ascending-descending bypass was performed because of re-coarctation. At admission, she presented with an ascending aortic aneurysm and a large pseudoaneurysm at the distal anastomosis of the previous extra-anatomic bypass that was itself partially thrombosed. The proximal descending aorta was highly narrowed . A small peripheral aorto-bronchial fistula was suspected as cause of the hemoptysis because it could not be identified during bronchoscopy. Operative repair was performed under double arterial canulation (aortic for the upper body and femoral artery for the lower body perfusion). The procedure was performed through mid-sternotomy and left hemi-clamshell and consisted in double ligation of the descending aorta proximally and distally of the end-to-side previous bypass anastomosis in order to exclude the pseudo-aneurysm. The ascending aortic aneurysm was resected and the aorta replaced with a prosthetic vascular graft and finally, an ascending-descending bypass was performed to restore continuity between the ascending with the distal descending aorta . The suspected site of the aorto-bronchial fistula was addressed by a small wedge-resection and the suture line covered with a intercostal muscle flap. Postoperative recovery was uneventful.
3.878906
0.98291
sec[1]/sec[5]/p[0]
en
0.999998
PMC9515373
https://doi.org/10.3389/fcvm.2022.920614
[ "ascending", "descending", "aortic", "bypass", "aorta", "because", "aneurysm", "hemoptysis", "coarctation", "repair" ]
[ { "code": "8C01.0", "title": "Acute inflammatory demyelinating polyneuropathy" }, { "code": "8A40.Z", "title": "Multiple sclerosis, unspecified" }, { "code": "LA8A.3", "title": "Congenital supravalvar aortic stenosis" }, { "code": "LA8B.2Y", "title": "Other specified congenital anomaly of aorta or its branches" }, { "code": "ND56.4", "title": "Injury of nerve of unspecified body region" }, { "code": "LB52.1", "title": "Undescended testicle, unilateral" }, { "code": "BD50.4Z", "title": "Abdominal aortic aneurysm, without mention of perforation or rupture" }, { "code": "2C80.Z", "title": "Malignant neoplasms of testis, unspecified" }, { "code": "LB52.2", "title": "Undescended testicle, bilateral" }, { "code": "2E92.4Y", "title": "Other specified benign neoplasm of the large intestine" } ]
=== ICD-11 CODES FOUND === [8C01.0] Acute inflammatory demyelinating polyneuropathy Definition: Progressive weakness of the limbs over a few days to 28 days, symmetrical deficit, areflexia, absent or mild sensory disturbance, elevated cerebrospinal fluid protein, and slowing of nerve conduction velocities are the cardinal features. The disorder may be preceded by upper respiratory or gastrointestinal infection or immunization 1 to 4 weeks prior to onset of the illness. Bifacial palsy may be present. Also known as: Acute inflammatory demyelinating polyneuropathy | Guillain-Barré syndrome | Guillain Barre syndrome | Acute Inflammatory Demyelinating Polyradiculoneuropathy | acute ascending paralysis Includes: Acute Inflammatory Demyelinating Polyradiculoneuropathy [8A40.Z] Multiple sclerosis, unspecified Also known as: Multiple sclerosis, unspecified | Multiple sclerosis | cerebrospinal sclerosis | disseminated sclerosis | generalised multiple sclerosis [LA8A.3] Congenital supravalvar aortic stenosis Definition: A congenital cardiovascular malformation with narrowing of the aorta at the level of the sinotubular junction which may extend into the ascending aorta. Additional information: 'Congenital supravalvar aortic stenosis' is described as three forms: an hourglass deformity, a fibrous membrane, and a diffuse narrowing of the ascending aorta. Supravalvar aortic stenosis may involve the coronary artery ostia, and the aortic leaflets may be tethered. The coronary arteries can become tortuous and dilate Also known as: Congenital supravalvar aortic stenosis | stenosis of aorta | supravalvular aortic stenosis | stricture of aorta | congenital narrowed aorta Excludes: Congenital aortic valvar stenosis [LA8B.2Y] Other specified congenital anomaly of aorta or its branches Also known as: Other specified congenital anomaly of aorta or its branches | Congenital anomaly of ascending aorta | Hypoplasia of ascending aorta | Congenital ascending aorta aneurysm or dilation | congenital ascending aortic aneurysm or dilation [ND56.4] Injury of nerve of unspecified body region Also known as: Injury of nerve of unspecified body region | injuries to nerves, nerve plexuses and roots | injury to nerves, unspecified site | nerve damage NOS | Injury of nerve NOS Excludes: multiple injuries of nerves NOS [LB52.1] Undescended testicle, unilateral Definition: The situation in which one of the two testicles in a male has not transitioned from the abdomen, and therefore appears absent from the scrotum. Also known as: Undescended testicle, unilateral | unilateral cryptorchidism | unilateral undescended testis | nondescent unilateral testicle | unilateral cryptorchism [BD50.4Z] Abdominal aortic aneurysm, without mention of perforation or rupture Also known as: Abdominal aortic aneurysm, without mention of perforation or rupture | Abdominal aortic aneurysm | abdomen aneurysm | abdominal aorta aneurysm | aneurysm of abdominal aorta [2C80.Z] Malignant neoplasms of testis, unspecified Also known as: Malignant neoplasms of testis, unspecified | Malignant neoplasms of testis | cancer of testis | testis cancer | malignant neoplasm of testis, NOS [LB52.2] Undescended testicle, bilateral Definition: The situation in which both testicles in a male have not transitioned from the abdomen, and therefore appear absent from the scrotum. Also known as: Undescended testicle, bilateral | bilateral cryptorchidism | bilateral cryptorchism | bilateral nondescent testicle | bilateral undescended testes [2E92.4Y] Other specified benign neoplasm of the large intestine Also known as: Other specified benign neoplasm of the large intestine | Benign neoplasm of appendix | benign tumour of appendix | Benign epithelial tumour of appendix | Hyperplastic polyp of appendix === GRAPH WALKS === --- Walk 1 --- [8C01.0] Acute inflammatory demyelinating polyneuropathy Def: Progressive weakness of the limbs over a few days to 28 days, symmetrical deficit, areflexia, absent or mild sensory disturbance, elevated cerebrospinal fluid protein, and slowing of nerve conduction ... --PARENT--> [8C01] Inflammatory polyneuropathy Def: Acquired inflammatory peripheral neuropathies are of a presumed immune etiology and are classified on the basis of their clinical course: acute inflammatory demyelinating polyneuropathy (AIDP or Guill... --CHILD--> [8C01.1] Post vaccinal neuropathy --- Walk 2 --- [8C01.0] Acute inflammatory demyelinating polyneuropathy Def: Progressive weakness of the limbs over a few days to 28 days, symmetrical deficit, areflexia, absent or mild sensory disturbance, elevated cerebrospinal fluid protein, and slowing of nerve conduction ... --PARENT--> [8C01] Inflammatory polyneuropathy Def: Acquired inflammatory peripheral neuropathies are of a presumed immune etiology and are classified on the basis of their clinical course: acute inflammatory demyelinating polyneuropathy (AIDP or Guill... --CHILD--> [8C01.2] Subacute inflammatory demyelinating polyneuropathy Def: Subacute inflammatory demyelinating polyneuropathy (SIDP) is a subacute progressive symmetric sensorial and/or motor disorder characterised by muscular weakness with impaired sensation, absent or dimi... --- Walk 3 --- [8A40.Z] Multiple sclerosis, unspecified --PARENT--> [8A40] Multiple sclerosis Def: Multiple Sclerosis (MS) is a chronic, inflammatory demyelinating disease of the central nervous system. Three categories of multiple sclerosis have been outlined: Relapsing/remitting, secondary progre... --CHILD--> [8A40.0] Relapsing-remitting multiple sclerosis Def: Clearly defined disease relapses with full recovery or with sequelae and residual deficit upon recovery. The periods between disease relapses are characterised by a lack of disease progression.... --- Walk 4 --- [8A40.Z] Multiple sclerosis, unspecified --PARENT--> [8A40] Multiple sclerosis Def: Multiple Sclerosis (MS) is a chronic, inflammatory demyelinating disease of the central nervous system. Three categories of multiple sclerosis have been outlined: Relapsing/remitting, secondary progre... --CHILD--> [8A40.1] Primary progressive multiple sclerosis Def: Disease progression from onset, with occasional plateaus and temporary minor improvements allowed.... --- Walk 5 --- [LA8A.3] Congenital supravalvar aortic stenosis Def: A congenital cardiovascular malformation with narrowing of the aorta at the level of the sinotubular junction which may extend into the ascending aorta. Additional information: 'Congenital supravalva... --EXCLUDES--> [?] Congenital aortic valvar stenosis Def: A congenital cardiovascular malformation of the aortic valve in which there is narrowing or stricture (obstruction to flow). Additional information: 'Congenital aortic valvar stenosis' arises most co... --EXCLUDES--> [?] Hypoplastic left heart syndrome Def: A spectrum of congenital cardiovascular malformations with normally aligned great arteries without a common atrioventricular junction, characterised by underdevelopment of the left heart with signific... --- Walk 6 --- [LA8A.3] Congenital supravalvar aortic stenosis Def: A congenital cardiovascular malformation with narrowing of the aorta at the level of the sinotubular junction which may extend into the ascending aorta. Additional information: 'Congenital supravalva... --EXCLUDES--> [?] Congenital aortic valvar stenosis Def: A congenital cardiovascular malformation of the aortic valve in which there is narrowing or stricture (obstruction to flow). Additional information: 'Congenital aortic valvar stenosis' arises most co... --EXCLUDES--> [?] Hypoplastic left heart syndrome Def: A spectrum of congenital cardiovascular malformations with normally aligned great arteries without a common atrioventricular junction, characterised by underdevelopment of the left heart with signific...
[ "[8C01.0] Acute inflammatory demyelinating polyneuropathy\n Def: Progressive weakness of the limbs over a few days to 28 days, symmetrical deficit, areflexia, absent or mild sensory disturbance, elevated cerebrospinal fluid protein, and slowing of nerve conduction ...\n --PARENT--> [8C01] Inflammatory polyneuropathy\n Def: Acquired inflammatory peripheral neuropathies are of a presumed immune etiology and are classified on the basis of their clinical course: acute inflammatory demyelinating polyneuropathy (AIDP or Guill...\n --CHILD--> [8C01.1] Post vaccinal neuropathy", "[8C01.0] Acute inflammatory demyelinating polyneuropathy\n Def: Progressive weakness of the limbs over a few days to 28 days, symmetrical deficit, areflexia, absent or mild sensory disturbance, elevated cerebrospinal fluid protein, and slowing of nerve conduction ...\n --PARENT--> [8C01] Inflammatory polyneuropathy\n Def: Acquired inflammatory peripheral neuropathies are of a presumed immune etiology and are classified on the basis of their clinical course: acute inflammatory demyelinating polyneuropathy (AIDP or Guill...\n --CHILD--> [8C01.2] Subacute inflammatory demyelinating polyneuropathy\n Def: Subacute inflammatory demyelinating polyneuropathy (SIDP) is a subacute progressive symmetric sensorial and/or motor disorder characterised by muscular weakness with impaired sensation, absent or dimi...", "[8A40.Z] Multiple sclerosis, unspecified\n --PARENT--> [8A40] Multiple sclerosis\n Def: Multiple Sclerosis (MS) is a chronic, inflammatory demyelinating disease of the central nervous system. Three categories of multiple sclerosis have been outlined: Relapsing/remitting, secondary progre...\n --CHILD--> [8A40.0] Relapsing-remitting multiple sclerosis\n Def: Clearly defined disease relapses with full recovery or with sequelae and residual deficit upon recovery. The periods between disease relapses are characterised by a lack of disease progression....", "[8A40.Z] Multiple sclerosis, unspecified\n --PARENT--> [8A40] Multiple sclerosis\n Def: Multiple Sclerosis (MS) is a chronic, inflammatory demyelinating disease of the central nervous system. Three categories of multiple sclerosis have been outlined: Relapsing/remitting, secondary progre...\n --CHILD--> [8A40.1] Primary progressive multiple sclerosis\n Def: Disease progression from onset, with occasional plateaus and temporary minor improvements allowed....", "[LA8A.3] Congenital supravalvar aortic stenosis\n Def: A congenital cardiovascular malformation with narrowing of the aorta at the level of the sinotubular junction which may extend into the ascending aorta.\n\nAdditional information: 'Congenital supravalva...\n --EXCLUDES--> [?] Congenital aortic valvar stenosis\n Def: A congenital cardiovascular malformation of the aortic valve in which there is narrowing or stricture (obstruction to flow).\n\nAdditional information: 'Congenital aortic valvar stenosis' arises most co...\n --EXCLUDES--> [?] Hypoplastic left heart syndrome\n Def: A spectrum of congenital cardiovascular malformations with normally aligned great arteries without a common atrioventricular junction, characterised by underdevelopment of the left heart with signific...", "[LA8A.3] Congenital supravalvar aortic stenosis\n Def: A congenital cardiovascular malformation with narrowing of the aorta at the level of the sinotubular junction which may extend into the ascending aorta.\n\nAdditional information: 'Congenital supravalva...\n --EXCLUDES--> [?] Congenital aortic valvar stenosis\n Def: A congenital cardiovascular malformation of the aortic valve in which there is narrowing or stricture (obstruction to flow).\n\nAdditional information: 'Congenital aortic valvar stenosis' arises most co...\n --EXCLUDES--> [?] Hypoplastic left heart syndrome\n Def: A spectrum of congenital cardiovascular malformations with normally aligned great arteries without a common atrioventricular junction, characterised by underdevelopment of the left heart with signific..." ]
8C01.0
Acute inflammatory demyelinating polyneuropathy
[ { "from_icd11": "8C01.0", "icd10_code": "G610", "icd10_title": "Guillain-Barre syndrome" }, { "from_icd11": "8A40.Z", "icd10_code": "G35", "icd10_title": "Multiple sclerosis" }, { "from_icd11": "8A40.Z", "icd10_code": "G370", "icd10_title": "Diffuse sclerosis of central nervous system" }, { "from_icd11": "8A40.Z", "icd10_code": "G375", "icd10_title": "Concentric sclerosis [Balo] of central nervous system" }, { "from_icd11": "LA8A.3", "icd10_code": "Q253", "icd10_title": "Supravalvular aortic stenosis" }, { "from_icd11": "ND56.4", "icd10_code": "T144", "icd10_title": "" }, { "from_icd11": "LB52.1", "icd10_code": "Q5310", "icd10_title": "Unspecified undescended testicle, unilateral" }, { "from_icd11": "LB52.1", "icd10_code": "Q53112", "icd10_title": "Unilateral inguinal testis" }, { "from_icd11": "LB52.1", "icd10_code": "Q531", "icd10_title": "Undescended testicle, unilateral" }, { "from_icd11": "LB52.1", "icd10_code": "Q5310 ", "icd10_title": "" }, { "from_icd11": "BD50.4Z", "icd10_code": "I714", "icd10_title": "Abdominal aortic aneurysm, without rupture" }, { "from_icd11": "2C80.Z", "icd10_code": "C6292", "icd10_title": "Malignant neoplasm of left testis, unspecified whether descended or undescended" }, { "from_icd11": "2C80.Z", "icd10_code": "C6212", "icd10_title": "Malignant neoplasm of descended left testis" }, { "from_icd11": "2C80.Z", "icd10_code": "C6290", "icd10_title": "Malignant neoplasm of unspecified testis, unspecified whether descended or undescended" }, { "from_icd11": "2C80.Z", "icd10_code": "C6211", "icd10_title": "Malignant neoplasm of descended right testis" } ]
G610
Guillain-Barre syndrome
Infective endocarditis (IE) due to nutritionally variant streptococci (NVS) is a very rare condition and is often associated with negative blood cultures. IE caused by NVS has a higher rate of complications compared to endocarditis caused by other streptococci . Over 100 cases of NVS infective endocarditis have been reported in the literature so far. NVS microorganisms have been found to be responsible for up to 6% of all cases of streptococcal endocarditis . IE induced by NVS is characterized by frequent relapses and a higher morbidity compared with infections induced by other species of streptococci. A clinical decision for rapid surgical intervention may be needed, especially in penicillin-resistant cases . Nevertheless, our case was culture-negative, and the surgical decision was made based on TTE and TEE results that clearly showed the presence of vegetations. Until metagenomic sequencing results became available, empirical therapy was initiated. After the pathogen was identified, a change in antibiotic treatment was appropriate, since previous data have showed that G. adiacens -infected IE patients experience a high rate of treatment success using ceftriaxone and gentamicin . After changing to G. adiacens -specific targeted therapy, the patient became afebrile and was in a good condition, symptomatically. No relapses were found on subsequent follow-up visits during the following six months.
4.207031
0.810547
sec[3]/p[0]
en
0.999997
PMC8950401
https://doi.org/10.3390/pathogens11030295
[ "endocarditis", "streptococci", "cases", "infective", "caused", "higher", "compared", "induced", "relapses", "decision" ]
[ { "code": "BC43.3", "title": "Endocardial fibroelastosis" }, { "code": "BB40", "title": "Acute or subacute infectious endocarditis" }, { "code": "BB4Z", "title": "Acute or subacute endocarditis, unspecified" }, { "code": "BB40&XN3NM", "title": "Streptococcal endocarditis" }, { "code": "1A72.Y/BB40", "title": "Gonococcal endocarditis" }, { "code": "QD0Y", "title": "Carrier of other specified infectious disease agent" }, { "code": "CA40.0Y", "title": "Pneumonia due to other specified bacteria" }, { "code": "KA61.Z", "title": "Bacterial infection of the fetus or newborn, unspecified" }, { "code": "JB20.Z", "title": "Single spontaneous delivery, unspecified" }, { "code": "QA48.0", "title": "Care or examination immediately after delivery" } ]
=== ICD-11 CODES FOUND === [BC43.3] Endocardial fibroelastosis Definition: Endocardial fibroelastosis is the formation of a marked fibro-elastic thickening of the subendocardium in one or both cardiac ventricles. A disorder of fetuses and infants, secondary causes include congenital left-sided obstructive cardiac lesions, metabolic disorders, autoimmune disease (anti-Ro/anti-La antibodies), and transplacental viral infection such as mumps. Primary endocardial fibroelastosis has been linked to recessive and x-linked inheritance, such as with Barth syndrome. Also known as: Endocardial fibroelastosis | elastomyofibrosis | endomyocardial fibroelastosis | EFE - [endocardial fibroelastosis] | primary endocardial fibroelastosis [BB40] Acute or subacute infectious endocarditis Also known as: Acute or subacute infectious endocarditis | subacute infective endocarditis NOS | infective endocarditis NOS | acute infective endocarditis NOS | infectious endocarditis Excludes: Infectious myocarditis [BB4Z] Acute or subacute endocarditis, unspecified Also known as: Acute or subacute endocarditis, unspecified | endocarditis acute or subacute | Acute or subacute pulmonary endocarditis | Acute or subacute aortic valve endocarditis | Acute or subacute mitral valve nonrheumatic endocarditis [QD0Y] Carrier of other specified infectious disease agent Also known as: Carrier of other specified infectious disease agent | Carrier of bacterial agents other than typhoid, diphtheria or intestinal infectious bacteria | carrier of other specified bacterial diseases | Carrier of meningococci | Carrier of staphylococci [CA40.0Y] Pneumonia due to other specified bacteria Also known as: Pneumonia due to other specified bacteria | Pneumonia due to Acinetobacter | Pneumonia due to other streptococci | streptococcal purulent pneumonia | streptococcal pneumonia [KA61.Z] Bacterial infection of the fetus or newborn, unspecified Also known as: Bacterial infection of the fetus or newborn, unspecified | Other bacterial infections of the fetus or newborn | congenital bacterial infections of newborn | Congenital clostridium infection | congenital clostridial infection [JB20.Z] Single spontaneous delivery, unspecified Also known as: Single spontaneous delivery, unspecified | Single spontaneous delivery | spontaneous delivery NOS | normal delivery NOS | uncomplicated delivery [QA48.0] Care or examination immediately after delivery Also known as: Care or examination immediately after delivery | care and observation in uncomplicated delivery cases | postpartum care immediately after delivery | postpartum examination immediately after delivery | Postpartum care after hospital delivery Excludes: Complications predominantly related to the puerperium === GRAPH WALKS === --- Walk 1 --- [BC43.3] Endocardial fibroelastosis Def: Endocardial fibroelastosis is the formation of a marked fibro-elastic thickening of the subendocardium in one or both cardiac ventricles. A disorder of fetuses and infants, secondary causes include co... --PARENT--> [BC43] Cardiomyopathy Def: These are myocardial disorders in which the heart muscle is structurally and functionally abnormal, in the absence of coronary artery disease, hypertension, valvular disease and congenital heart disea... --RELATED_TO--> [?] Cardiomyopathy in the puerperium Def: A group of diseases in which the dominant feature is the involvement of the cardiac muscle itself occurring in puerperium, the period of 6-8 weeks after giving birth. Cardiomyopathies are classified a... --- Walk 2 --- [BC43.3] Endocardial fibroelastosis Def: Endocardial fibroelastosis is the formation of a marked fibro-elastic thickening of the subendocardium in one or both cardiac ventricles. A disorder of fetuses and infants, secondary causes include co... --PARENT--> [BC43] Cardiomyopathy Def: These are myocardial disorders in which the heart muscle is structurally and functionally abnormal, in the absence of coronary artery disease, hypertension, valvular disease and congenital heart disea... --RELATED_TO--> [?] Pacing-induced cardiomyopathy Def: Pacing-induced cardiomyopathy is ventricular dilation, dysfunction (systolic and/or diastolic) and dyskinesia associated with chronic ventricular pacing in the absence of other causes of cardiomyopath... --- Walk 3 --- [BB40] Acute or subacute infectious endocarditis --RELATED_TO--> [?] Endocardial fibroelastosis Def: Endocardial fibroelastosis is the formation of a marked fibro-elastic thickening of the subendocardium in one or both cardiac ventricles. A disorder of fetuses and infants, secondary causes include co... --CHILD--> [?] Congenital endocarditis --- Walk 4 --- [BB40] Acute or subacute infectious endocarditis --RELATED_TO--> [?] Endocardial fibroelastosis Def: Endocardial fibroelastosis is the formation of a marked fibro-elastic thickening of the subendocardium in one or both cardiac ventricles. A disorder of fetuses and infants, secondary causes include co... --CHILD--> [?] Congenital endocarditis --- Walk 5 --- [BB4Z] Acute or subacute endocarditis, unspecified --PARENT--> [?] Acute or subacute endocarditis Def: A condition characterised by inflammation of endocardium... --RELATED_TO--> [?] Typhoid fever with heart involvement Def: This is a common worldwide bacterial disease, transmitted by the ingestion of food or water contaminated with the faeces of an infected person, which contain the bacterium Salmonella typhi, serotype T... --- Walk 6 --- [BB4Z] Acute or subacute endocarditis, unspecified --PARENT--> [?] Acute or subacute endocarditis Def: A condition characterised by inflammation of endocardium... --CHILD--> [BB41] Myoendocarditis
[ "[BC43.3] Endocardial fibroelastosis\n Def: Endocardial fibroelastosis is the formation of a marked fibro-elastic thickening of the subendocardium in one or both cardiac ventricles. A disorder of fetuses and infants, secondary causes include co...\n --PARENT--> [BC43] Cardiomyopathy\n Def: These are myocardial disorders in which the heart muscle is structurally and functionally abnormal, in the absence of coronary artery disease, hypertension, valvular disease and congenital heart disea...\n --RELATED_TO--> [?] Cardiomyopathy in the puerperium\n Def: A group of diseases in which the dominant feature is the involvement of the cardiac muscle itself occurring in puerperium, the period of 6-8 weeks after giving birth. Cardiomyopathies are classified a...", "[BC43.3] Endocardial fibroelastosis\n Def: Endocardial fibroelastosis is the formation of a marked fibro-elastic thickening of the subendocardium in one or both cardiac ventricles. A disorder of fetuses and infants, secondary causes include co...\n --PARENT--> [BC43] Cardiomyopathy\n Def: These are myocardial disorders in which the heart muscle is structurally and functionally abnormal, in the absence of coronary artery disease, hypertension, valvular disease and congenital heart disea...\n --RELATED_TO--> [?] Pacing-induced cardiomyopathy\n Def: Pacing-induced cardiomyopathy is ventricular dilation, dysfunction (systolic and/or diastolic) and dyskinesia associated with chronic ventricular pacing in the absence of other causes of cardiomyopath...", "[BB40] Acute or subacute infectious endocarditis\n --RELATED_TO--> [?] Endocardial fibroelastosis\n Def: Endocardial fibroelastosis is the formation of a marked fibro-elastic thickening of the subendocardium in one or both cardiac ventricles. A disorder of fetuses and infants, secondary causes include co...\n --CHILD--> [?] Congenital endocarditis", "[BB40] Acute or subacute infectious endocarditis\n --RELATED_TO--> [?] Endocardial fibroelastosis\n Def: Endocardial fibroelastosis is the formation of a marked fibro-elastic thickening of the subendocardium in one or both cardiac ventricles. A disorder of fetuses and infants, secondary causes include co...\n --CHILD--> [?] Congenital endocarditis", "[BB4Z] Acute or subacute endocarditis, unspecified\n --PARENT--> [?] Acute or subacute endocarditis\n Def: A condition characterised by inflammation of endocardium...\n --RELATED_TO--> [?] Typhoid fever with heart involvement\n Def: This is a common worldwide bacterial disease, transmitted by the ingestion of food or water contaminated with the faeces of an infected person, which contain the bacterium Salmonella typhi, serotype T...", "[BB4Z] Acute or subacute endocarditis, unspecified\n --PARENT--> [?] Acute or subacute endocarditis\n Def: A condition characterised by inflammation of endocardium...\n --CHILD--> [BB41] Myoendocarditis" ]
BC43.3
Endocardial fibroelastosis
[ { "from_icd11": "BC43.3", "icd10_code": "I424", "icd10_title": "Endocardial fibroelastosis" }, { "from_icd11": "BB40", "icd10_code": "I330", "icd10_title": "Acute and subacute infective endocarditis" }, { "from_icd11": "BB4Z", "icd10_code": "I38", "icd10_title": "Endocarditis, valve unspecified" }, { "from_icd11": "BB4Z", "icd10_code": "I339", "icd10_title": "Acute and subacute endocarditis, unspecified" }, { "from_icd11": "BB4Z", "icd10_code": "I33", "icd10_title": "Acute and subacute endocarditis" }, { "from_icd11": "JB20.Z", "icd10_code": "O80", "icd10_title": "Encounter for full-term uncomplicated delivery" }, { "from_icd11": "JB20.Z", "icd10_code": "O808", "icd10_title": "" }, { "from_icd11": "JB20.Z", "icd10_code": "O809", "icd10_title": "" }, { "from_icd11": "QA48.0", "icd10_code": "Z390", "icd10_title": "Encounter for care and examination of mother immediately after delivery" } ]
I424
Endocardial fibroelastosis
The patient was evaluated for epilepsy surgery but was found to have normal brain magnetic resonance imaging (MRI), normal brain positron emission tomography (PET) scan, an inconclusive ictal single-photon emission computerized tomography (SPECT) scan, and a magnetoencephalogram (MEG) showing left greater than right bi-frontal epileptiform discharges. After discussion in a multidisciplinary patient management conference, a vagus nerve stimulator (VNS) was implanted. With medication changes and VNS implantation , the frequency, intensity and duration of seizures improved, but he continued to have 1–2 seizures/night despite maximal tolerable medication dosing and VNS management. Subsequent next-generation genetic sequencing (Invitae Epilepsy Panel, 146 genes) revealed the heterozygous variant c.851C>G in the CHRNA4 gene resulting in the missense mutation p.Ser284Trp within the α4 subunit α4β2 nAChR, classified by the laboratory as a variant of uncertain significance. The α4-Ser284 residue is conserved among CHRNA4 genes from vertebrate species, as well as human CHRNA1 through CHRNA7 genes . Located within the M2 transmembrane α-helix that lines the ion channel, α4-Ser284Trp maps onto the cryo-electron microscopic structure of the α4β2 nAChR such that the large Trp sidechain impinges upon the M2 transmembrane α-helix from the neighboring subunit in a manner that would promote expansion of the pore .
4.257813
0.857422
sec[1]/sec[0]/p[1]
en
0.999997
PMC9602795
https://doi.org/10.3390/ijms232012124
[ "genes", "that", "epilepsy", "brain", "emission", "tomography", "scan", "medication", "seizures", "variant" ]
[ { "code": "9A70.Y", "title": "Other specified hereditary corneal dystrophies" }, { "code": "GB81", "title": "Autosomal dominant polycystic kidney disease" }, { "code": "8A02.12", "title": "Dystonia associated with heredodegenerative disorders" }, { "code": "5C50.E0", "title": "Classical organic aciduria" }, { "code": "8E02.0", "title": "Genetic Creutzfeldt-Jakob disease" }, { "code": "8A80.Z", "title": "Migraine, unspecified" }, { "code": "QA76", "title": "Medication or substance that is known to be an allergen without injury or harm" }, { "code": "PL13.6", "title": "Medication or substance that is known to be an allergen, as mode of injury or harm" }, { "code": "9C40.A0", "title": "Papilloedema" }, { "code": "PA6Z", "title": "Unintentional fall from unspecified height" } ]
=== ICD-11 CODES FOUND === [9A70.Y] Other specified hereditary corneal dystrophies Also known as: Other specified hereditary corneal dystrophies | Epithelial juvenile corneal dystrophy | TGFBI - [transforming growth factor beta-induced] gene | Granular corneal dystrophy | granular-lattice corneal dystrophy Includes: Granular corneal dystrophy [GB81] Autosomal dominant polycystic kidney disease Definition: Multiple cysts in both kidneys increasing in number and size from adolescence, associated with development of hypertension and chronic renal failure. Autosomal dominant familial pattern is usual and due to mutations on chromosomes 16 and 4. Non-renal manifestations can include cysts in the liver and less commonly pancreas. Cerebral arterial aneurysms with subarachnoid haemorrhage, and other non-renal vascular abnormalities can also occur. Also known as: Autosomal dominant polycystic kidney disease | adult polycystic kidney disease | Polycystic kidney, adult type | APCKD - [autosomal polycystic kidney disease] | Autosomal dominant polycystic kidney disease type 1 without tuberous sclerosis [8A02.12] Dystonia associated with heredodegenerative disorders Definition: Dystonia occurring as a part of a more complex heredodegenerative disorder. It is not a pure dystonia and other neurological findings such as ataxia, pyramidal signs and cognitive issues may be seen. Also known as: Dystonia associated with heredodegenerative disorders | Dystonia due to autosomal dominant disorders | Rapid-onset dystonia-parkinsonism | Dystonia due to dentatorubropallidoluysian atrophy | Dystonia due to Huntington disease [5C50.E0] Classical organic aciduria Definition: This a term used to classify a group of metabolic disorders which disrupt normal amino acid metabolism, particularly branched-chain amino acids, causing a buildup of acids which are usually not present. Also known as: Classical organic aciduria | Methylmalonic aciduria - homocystinuria | Methylmalonic acidaemia - homocystinuria | Methylmalonic aciduria - homocystinuria type cbl C | Methylmalonic acidaemia - homocystinuria type cbl C [8E02.0] Genetic Creutzfeldt-Jakob disease Definition: A disease of the brain, that is associated with a prion. This disease is characterised by neurological deficits, and is fatal. Confirmation is by pathological examination of the brain. Also known as: Genetic Creutzfeldt-Jakob disease | CJD - [Creutzfeldt-Jakob disease] | Creutzfeldt-Jakob | Creutzfeldt-Jakob disease | JCD - [Jakob-Creutzfeldt disease] [8A80.Z] Migraine, unspecified Also known as: Migraine, unspecified | Migraine [QA76] Medication or substance that is known to be an allergen without injury or harm Definition: Medication that has previously been identified as an allergen to the patient is administered, but does not result in injury or harm. Also known as: Medication or substance that is known to be an allergen without injury or harm Excludes: Medication or substance that is known to be an allergen, as mode of injury or harm [PL13.6] Medication or substance that is known to be an allergen, as mode of injury or harm Also known as: Medication or substance that is known to be an allergen, as mode of injury or harm | medication error relating to known allergy to drug or substance | adverse drug event relating to known allergy to drug or substance [9C40.A0] Papilloedema Definition: Optic disc swelling that results from increased intracranial pressure Also known as: Papilloedema | Optic disc swelling that results from increased intracranial pressure Includes: Optic disc swelling that results from increased intracranial pressure [PA6Z] Unintentional fall from unspecified height Also known as: Unintentional fall from unspecified height | fall NOS | accidental fall | fall causing injury that resulted in death | fell NOS === GRAPH WALKS === --- Walk 1 --- [9A70.Y] Other specified hereditary corneal dystrophies --PARENT--> [9A70] Hereditary corneal dystrophies Def: The term corneal dystrophy embraces a heterogeneous group of bilateral genetically determined non-inflammatory corneal diseases that are usually restricted to the cornea. The designation is imprecise ... --CHILD--> [9A70.Z] Hereditary corneal dystrophies, unspecified --- Walk 2 --- [9A70.Y] Other specified hereditary corneal dystrophies --PARENT--> [9A70] Hereditary corneal dystrophies Def: The term corneal dystrophy embraces a heterogeneous group of bilateral genetically determined non-inflammatory corneal diseases that are usually restricted to the cornea. The designation is imprecise ... --RELATED_TO--> [?] X-linked ichthyosis Def: X-linked ichthyosis is an X-linked recessive genodermatosis associated with steroid sulfatase deficiency and elevated plasma cholesterol sulfate. Generalised scaling is present at or shortly after bir... --- Walk 3 --- [GB81] Autosomal dominant polycystic kidney disease Def: Multiple cysts in both kidneys increasing in number and size from adolescence, associated with development of hypertension and chronic renal failure. Autosomal dominant familial pattern is usual and d... --PARENT--> [?] Cystic or dysplastic kidney disease Def: Any disease of the kidney, caused by determinants arising during the antenatal period or after birth. These diseases are characterised by pathological changes to one or both kidneys, and may manifest ... --CHILD--> [GB80] Nonfamilial nongenetic cystic kidney disease Def: Diseases where there are developmental anatomical or pathological changes in the renal substance not occurring in a familial distribution and not known to have a mono-genetic cause.... --- Walk 4 --- [GB81] Autosomal dominant polycystic kidney disease Def: Multiple cysts in both kidneys increasing in number and size from adolescence, associated with development of hypertension and chronic renal failure. Autosomal dominant familial pattern is usual and d... --PARENT--> [?] Cystic or dysplastic kidney disease Def: Any disease of the kidney, caused by determinants arising during the antenatal period or after birth. These diseases are characterised by pathological changes to one or both kidneys, and may manifest ... --RELATED_TO--> [?] Tuberous sclerosis Def: A disease caused by a dominant mutation of 9q34 (TSC1) or 16p13 (TSC2). This disease may present with facial angiofibromas, Koenen tumours, fibrous plaques on the forehead and scalp, renal angiomyolip... --- Walk 5 --- [8A02.12] Dystonia associated with heredodegenerative disorders Def: Dystonia occurring as a part of a more complex heredodegenerative disorder. It is not a pure dystonia and other neurological findings such as ataxia, pyramidal signs and cognitive issues may be seen.... --PARENT--> [8A02.1] Secondary dystonia Def: This is dystonia – a disorder of involuntary muscle contractions – of an acquired nature. Causes include substance toxicity, injury, hypoxia and tumours.... --CHILD--> [8A02.11] Dystonia-plus Def: This is a group of heterogenous syndromes present with dystonia – a disorder of involuntary muscle contractions – along with other clinical features, but not in tandem with a neurodegenerative disease... --- Walk 6 --- [8A02.12] Dystonia associated with heredodegenerative disorders Def: Dystonia occurring as a part of a more complex heredodegenerative disorder. It is not a pure dystonia and other neurological findings such as ataxia, pyramidal signs and cognitive issues may be seen.... --PARENT--> [8A02.1] Secondary dystonia Def: This is dystonia – a disorder of involuntary muscle contractions – of an acquired nature. Causes include substance toxicity, injury, hypoxia and tumours.... --CHILD--> [8A02.10] Drug-induced dystonia Def: This is dystonia due to medications either as an idiosyncratic side effect or due to overdose of medications....
[ "[9A70.Y] Other specified hereditary corneal dystrophies\n --PARENT--> [9A70] Hereditary corneal dystrophies\n Def: The term corneal dystrophy embraces a heterogeneous group of bilateral genetically determined non-inflammatory corneal diseases that are usually restricted to the cornea. The designation is imprecise ...\n --CHILD--> [9A70.Z] Hereditary corneal dystrophies, unspecified", "[9A70.Y] Other specified hereditary corneal dystrophies\n --PARENT--> [9A70] Hereditary corneal dystrophies\n Def: The term corneal dystrophy embraces a heterogeneous group of bilateral genetically determined non-inflammatory corneal diseases that are usually restricted to the cornea. The designation is imprecise ...\n --RELATED_TO--> [?] X-linked ichthyosis\n Def: X-linked ichthyosis is an X-linked recessive genodermatosis associated with steroid sulfatase deficiency and elevated plasma cholesterol sulfate. Generalised scaling is present at or shortly after bir...", "[GB81] Autosomal dominant polycystic kidney disease\n Def: Multiple cysts in both kidneys increasing in number and size from adolescence, associated with development of hypertension and chronic renal failure. Autosomal dominant familial pattern is usual and d...\n --PARENT--> [?] Cystic or dysplastic kidney disease\n Def: Any disease of the kidney, caused by determinants arising during the antenatal period or after birth. These diseases are characterised by pathological changes to one or both kidneys, and may manifest ...\n --CHILD--> [GB80] Nonfamilial nongenetic cystic kidney disease\n Def: Diseases where there are developmental anatomical or pathological changes in the renal substance not occurring in a familial distribution and not known to have a mono-genetic cause....", "[GB81] Autosomal dominant polycystic kidney disease\n Def: Multiple cysts in both kidneys increasing in number and size from adolescence, associated with development of hypertension and chronic renal failure. Autosomal dominant familial pattern is usual and d...\n --PARENT--> [?] Cystic or dysplastic kidney disease\n Def: Any disease of the kidney, caused by determinants arising during the antenatal period or after birth. These diseases are characterised by pathological changes to one or both kidneys, and may manifest ...\n --RELATED_TO--> [?] Tuberous sclerosis\n Def: A disease caused by a dominant mutation of 9q34 (TSC1) or 16p13 (TSC2). This disease may present with facial angiofibromas, Koenen tumours, fibrous plaques on the forehead and scalp, renal angiomyolip...", "[8A02.12] Dystonia associated with heredodegenerative disorders\n Def: Dystonia occurring as a part of a more complex heredodegenerative disorder. It is not a pure dystonia and other neurological findings such as ataxia, pyramidal signs and cognitive issues may be seen....\n --PARENT--> [8A02.1] Secondary dystonia\n Def: This is dystonia – a disorder of involuntary muscle contractions – of an acquired nature. Causes include substance toxicity, injury, hypoxia and tumours....\n --CHILD--> [8A02.11] Dystonia-plus\n Def: This is a group of heterogenous syndromes present with dystonia – a disorder of involuntary muscle contractions – along with other clinical features, but not in tandem with a neurodegenerative disease...", "[8A02.12] Dystonia associated with heredodegenerative disorders\n Def: Dystonia occurring as a part of a more complex heredodegenerative disorder. It is not a pure dystonia and other neurological findings such as ataxia, pyramidal signs and cognitive issues may be seen....\n --PARENT--> [8A02.1] Secondary dystonia\n Def: This is dystonia – a disorder of involuntary muscle contractions – of an acquired nature. Causes include substance toxicity, injury, hypoxia and tumours....\n --CHILD--> [8A02.10] Drug-induced dystonia\n Def: This is dystonia due to medications either as an idiosyncratic side effect or due to overdose of medications...." ]
9A70.Y
Other specified hereditary corneal dystrophies
[ { "from_icd11": "GB81", "icd10_code": "Q612", "icd10_title": "Polycystic kidney, adult type" }, { "from_icd11": "8E02.0", "icd10_code": "A8100", "icd10_title": "Creutzfeldt-Jakob disease, unspecified" }, { "from_icd11": "8E02.0", "icd10_code": "A8109", "icd10_title": "Other Creutzfeldt-Jakob disease" }, { "from_icd11": "8E02.0", "icd10_code": "A810", "icd10_title": "Creutzfeldt-Jakob disease" }, { "from_icd11": "8A80.Z", "icd10_code": "G43B0", "icd10_title": "Ophthalmoplegic migraine, not intractable" }, { "from_icd11": "8A80.Z", "icd10_code": "G43409", "icd10_title": "Hemiplegic migraine, not intractable, without status migrainosus" }, { "from_icd11": "8A80.Z", "icd10_code": "G43A0", "icd10_title": "Cyclical vomiting, in migraine, not intractable" }, { "from_icd11": "8A80.Z", "icd10_code": "G43D0", "icd10_title": "Abdominal migraine, not intractable" }, { "from_icd11": "8A80.Z", "icd10_code": "G43709", "icd10_title": "Chronic migraine without aura, not intractable, without status migrainosus" }, { "from_icd11": "8A80.Z", "icd10_code": "G43A1", "icd10_title": "Cyclical vomiting, in migraine, intractable" }, { "from_icd11": "8A80.Z", "icd10_code": "G43509", "icd10_title": "Persistent migraine aura without cerebral infarction, not intractable, without status migrainosus" }, { "from_icd11": "8A80.Z", "icd10_code": "G43719", "icd10_title": "Chronic migraine without aura, intractable, without status migrainosus" }, { "from_icd11": "8A80.Z", "icd10_code": "G43501", "icd10_title": "Persistent migraine aura without cerebral infarction, not intractable, with status migrainosus" }, { "from_icd11": "8A80.Z", "icd10_code": "G43C0", "icd10_title": "Periodic headache syndromes in child or adult, not intractable" }, { "from_icd11": "8A80.Z", "icd10_code": "G43401", "icd10_title": "Hemiplegic migraine, not intractable, with status migrainosus" } ]
Q612
Polycystic kidney, adult type
Saddle pulmonary embolism (SPE) represents a rare type of venous thromboembolism that occurs in approximately 2.6–5.4% of all acute pulmonary embolism (PE) cases and frequently leads to hemodynamic collapse and sudden death [ 1 – 4 ]. As conventional reperfusion therapy including thrombolysis and thrombectomy is less efficacious in mitigating hemodynamic instability, venoarterial extracorporeal membrane oxygenation (VA-ECMO) has increasingly emerged as a salvage therapy for PE-induced hemodynamic instability, which is typically defined as persistent hypotension, obstructive shock, or cardiac arrest . Despite this, the appropriate selection of patients eligible for VA-ECMO remains an ongoing challenge in clinical practice. This is especially true for advanced malignancy patients with brain metastases given the potential bleeding complications and uncertain prognosis . Immunosuppression and irreversible central nervous system pathology have historically been considered to be relatively contraindicated to the application of extracorporeal membrane oxygenation (ECMO) . Consequently, despite a largely increased number of ECMO runs over the past decade, the ECMO runs for neoplasms remain quite infrequent . Herein, we reported a rare case describing the successful management of hemodynamic deterioration secondary to SPE-induced cardiac arrest using VA-ECMO in a lung cancer patient with brain metastases.
4.238281
0.87793
sec[0]/p[0]
en
0.999997
PMC9720990
https://doi.org/10.1186/s13019-022-02044-w
[ "ecmo", "hemodynamic", "pulmonary", "embolism", "rare", "instability", "extracorporeal", "membrane", "oxygenation", "induced" ]
[ { "code": "PK81.1", "title": "Extracorporeal life support procedure associated with injury or harm in therapeutic use" }, { "code": "QC48.Y", "title": "Other specified personal history of medical treatment" }, { "code": "LA88.42", "title": "Ventricular septal defect haemodynamically insignificant" }, { "code": "CB40.Y", "title": "Other specified diseases of the respiratory system" }, { "code": "LA75.1", "title": "Agenesis of lung" }, { "code": "CA40.Z", "title": "Pneumonia, organism unspecified" }, { "code": "CB41", "title": "Respiratory failure" }, { "code": "NB32.3Y", "title": "Other injury of lung" }, { "code": "DD30.Z", "title": "Acute vascular disorders of intestine, unspecified" }, { "code": "JB42.2", "title": "Obstetric blood-clot embolism" } ]
=== ICD-11 CODES FOUND === [PK81.1] Extracorporeal life support procedure associated with injury or harm in therapeutic use Also known as: Extracorporeal life support procedure associated with injury or harm in therapeutic use | ECMO - [extracorporeal membrane oxygenation] | complication during or following extracorporeal life support procedure Excludes: Circumstances associated with a surgical or other medical procedure influencing the episode of care, without injury or harm [QC48.Y] Other specified personal history of medical treatment Also known as: Other specified personal history of medical treatment | Personal history of contraception | history of contraception | Personal history of long-term use of medicaments other than anticoagulants | personal history of long term current use of medicaments [LA88.42] Ventricular septal defect haemodynamically insignificant Definition: A congenital cardiac malformation in which there is one or more small, clinically insignificant ventricular septal defect(s) in the absence of flow-related cardiac chamber dilation or abnormal elevation of pulmonary arterial pressure. Additional information: though restrictive ventricular septal defect is listed as a synonym of haemodynamically insignificant VSD, it should be recognised that some pressure restrictive ventricular septal defects will lead to flow-related chamber dilation, and thu Also known as: Ventricular septal defect haemodynamically insignificant | Maladie de Roger | restrictive ventricular septal defect [CB40.Y] Other specified diseases of the respiratory system Also known as: Other specified diseases of the respiratory system | Secondary respiratory disorders | Respiratory disorders in diseases classified elsewhere | Diseases of bronchus, not elsewhere classified | Acquired bronchial diverticulum [LA75.1] Agenesis of lung Definition: This refers to the absence or rudimentary residua of an undeveloped lung. Also known as: Agenesis of lung | Pulmonary agenesis | absence of lung | aplasia of lung | apulmonism [CA40.Z] Pneumonia, organism unspecified Also known as: Pneumonia, organism unspecified | Pneumonia | infectious pneumonia | PN - [pneumonia] | lobar pneumonia NOS [CB41] Respiratory failure Definition: Respiratory failure is a life-threatening impairment of oxygenation or carbon dioxide (CO2) elimination. Respiratory failure may occur because of impaired gas exchange, decreased ventilation, or both. The level of oxygen in the blood becomes dangerously low or the level of carbon dioxide becomes dangerously high. Also known as: Respiratory failure | lung failure NOS | pulmonary failure Excludes: Acute respiratory distress syndrome | Respiratory arrest | Respiratory distress of newborn [NB32.3Y] Other injury of lung Also known as: Other injury of lung | Haematoma of lung | Traumatic hydropneumothorax | Acute traumatic lung congestion | Rupture of lung [DD30.Z] Acute vascular disorders of intestine, unspecified Also known as: Acute vascular disorders of intestine, unspecified | Acute vascular disorders of intestine | acute intestinal ischemia NOS | acute intestinal ischemic syndrome | acute ischaemic bowel disease [JB42.2] Obstetric blood-clot embolism Definition: A condition characterised by the lodging of a blood clot (a specific type of embolus known as a thrombus) in the bloodstream, which can cause a blockage associated with the physiological and other changes that occur during the period of time from conception to delivery (pregnancy), during labour and delivery (childbirth) or during the approximately six weeks after delivery during which the uterus returns to the original size (puerperium). Also known as: Obstetric blood-clot embolism | obstetrical blood-clot embolism | blood clot embolism in pregnancy, childbirth or puerperium | puerperal embolism | Puerperal embolism NOS === GRAPH WALKS === --- Walk 1 --- [PK81.1] Extracorporeal life support procedure associated with injury or harm in therapeutic use --EXCLUDES--> [?] Circumstances associated with a surgical or other medical procedure influencing the episode of care, without injury or harm --CHILD--> [?] Foreign body accidentally left in body without injury or harm Def: A foreign body is any solid material not normally found in the human body. It is accidentally left in the body if there was no specific intention to keep it in the body.... --- Walk 2 --- [PK81.1] Extracorporeal life support procedure associated with injury or harm in therapeutic use --PARENT--> [PK81] Certain medical procedures associated with injury or harm in therapeutic use --CHILD--> [PK81.0] Ventilation associated with injury or harm in therapeutic use --- Walk 3 --- [QC48.Y] Other specified personal history of medical treatment --PARENT--> [QC48] Personal history of medical treatment --PARENT--> [?] Personal history of health problems --- Walk 4 --- [QC48.Y] Other specified personal history of medical treatment --PARENT--> [QC48] Personal history of medical treatment --CHILD--> [QC48.Z] Personal history of medical treatment, unspecified --- Walk 5 --- [LA88.42] Ventricular septal defect haemodynamically insignificant Def: A congenital cardiac malformation in which there is one or more small, clinically insignificant ventricular septal defect(s) in the absence of flow-related cardiac chamber dilation or abnormal elevati... --PARENT--> [LA88.4] Ventricular septal defect Def: A congenital cardiac malformation in which there is a hole or pathway between the ventricular chambers.... --CHILD--> [LA88.42] Ventricular septal defect haemodynamically insignificant Def: A congenital cardiac malformation in which there is one or more small, clinically insignificant ventricular septal defect(s) in the absence of flow-related cardiac chamber dilation or abnormal elevati... --- Walk 6 --- [LA88.42] Ventricular septal defect haemodynamically insignificant Def: A congenital cardiac malformation in which there is one or more small, clinically insignificant ventricular septal defect(s) in the absence of flow-related cardiac chamber dilation or abnormal elevati... --PARENT--> [LA88.4] Ventricular septal defect Def: A congenital cardiac malformation in which there is a hole or pathway between the ventricular chambers.... --PARENT--> [LA88] Congenital anomaly of a ventricle or the ventricular septum Def: A congenital cardiac malformation in which there is an abnormality of a ventricle and/or the ventricular septum. The ventricles include the ventricular inlet, ventricular body and ventricular outflow ...
[ "[PK81.1] Extracorporeal life support procedure associated with injury or harm in therapeutic use\n --EXCLUDES--> [?] Circumstances associated with a surgical or other medical procedure influencing the episode of care, without injury or harm\n --CHILD--> [?] Foreign body accidentally left in body without injury or harm\n Def: A foreign body is any solid material not normally found in the human body. It is accidentally left in the body if there was no specific intention to keep it in the body....", "[PK81.1] Extracorporeal life support procedure associated with injury or harm in therapeutic use\n --PARENT--> [PK81] Certain medical procedures associated with injury or harm in therapeutic use\n --CHILD--> [PK81.0] Ventilation associated with injury or harm in therapeutic use", "[QC48.Y] Other specified personal history of medical treatment\n --PARENT--> [QC48] Personal history of medical treatment\n --PARENT--> [?] Personal history of health problems", "[QC48.Y] Other specified personal history of medical treatment\n --PARENT--> [QC48] Personal history of medical treatment\n --CHILD--> [QC48.Z] Personal history of medical treatment, unspecified", "[LA88.42] Ventricular septal defect haemodynamically insignificant\n Def: A congenital cardiac malformation in which there is one or more small, clinically insignificant ventricular septal defect(s) in the absence of flow-related cardiac chamber dilation or abnormal elevati...\n --PARENT--> [LA88.4] Ventricular septal defect\n Def: A congenital cardiac malformation in which there is a hole or pathway between the ventricular chambers....\n --CHILD--> [LA88.42] Ventricular septal defect haemodynamically insignificant\n Def: A congenital cardiac malformation in which there is one or more small, clinically insignificant ventricular septal defect(s) in the absence of flow-related cardiac chamber dilation or abnormal elevati...", "[LA88.42] Ventricular septal defect haemodynamically insignificant\n Def: A congenital cardiac malformation in which there is one or more small, clinically insignificant ventricular septal defect(s) in the absence of flow-related cardiac chamber dilation or abnormal elevati...\n --PARENT--> [LA88.4] Ventricular septal defect\n Def: A congenital cardiac malformation in which there is a hole or pathway between the ventricular chambers....\n --PARENT--> [LA88] Congenital anomaly of a ventricle or the ventricular septum\n Def: A congenital cardiac malformation in which there is an abnormality of a ventricle and/or the ventricular septum. The ventricles include the ventricular inlet, ventricular body and ventricular outflow ..." ]
PK81.1
Extracorporeal life support procedure associated with injury or harm in therapeutic use
[ { "from_icd11": "QC48.Y", "icd10_code": "Z794", "icd10_title": "Long term (current) use of insulin" }, { "from_icd11": "QC48.Y", "icd10_code": "Z7902", "icd10_title": "Long term (current) use of antithrombotics/antiplatelets" }, { "from_icd11": "QC48.Y", "icd10_code": "Z7982", "icd10_title": "Long term (current) use of aspirin" }, { "from_icd11": "QC48.Y", "icd10_code": "Z7984", "icd10_title": "Long term (current) use of oral hypoglycemic drugs" }, { "from_icd11": "QC48.Y", "icd10_code": "Z79899", "icd10_title": "Other long term (current) drug therapy" }, { "from_icd11": "LA75.1", "icd10_code": "Q333", "icd10_title": "Agenesis of lung" }, { "from_icd11": "CA40.Z", "icd10_code": "J189", "icd10_title": "Pneumonia, unspecified organism" }, { "from_icd11": "CA40.Z", "icd10_code": "J181", "icd10_title": "Lobar pneumonia, unspecified organism" }, { "from_icd11": "CA40.Z", "icd10_code": "J188", "icd10_title": "Other pneumonia, unspecified organism" }, { "from_icd11": "CA40.Z", "icd10_code": "J168", "icd10_title": "Pneumonia due to other specified infectious organisms" }, { "from_icd11": "CA40.Z", "icd10_code": "J180", "icd10_title": "Bronchopneumonia, unspecified organism" }, { "from_icd11": "CA40.Z", "icd10_code": "J17", "icd10_title": "Pneumonia in diseases classified elsewhere" }, { "from_icd11": "CA40.Z", "icd10_code": "J182", "icd10_title": "Hypostatic pneumonia, unspecified organism" }, { "from_icd11": "CA40.Z", "icd10_code": "J16", "icd10_title": "Pneumonia due to other infectious organisms, not elsewhere classified" }, { "from_icd11": "CA40.Z", "icd10_code": "J171", "icd10_title": "" } ]
Z794
Long term (current) use of insulin
Entering visual acuity with spectacles was 20/125 −1 with pinhole potential to 20/50 +1 for the right eye, and 20/250 for the left eye with pinhole potential to 20/100 −1 . Slit lamp evaluation revealed severe keratinization of the lid margins, bulbar conjunctiva, and palpebral conjunctiva for both eyes. A symblepharon was noted nasally in both the right and left eye, left eye worse than right. All four puncta were scarred. The right cornea revealed grade 2 neovascularization, while the left cornea was more severe with grade 3 neovascularization. Corneal opacification for the right eye was grade 2, with iris details poorly seen with pupil margin just visible . The corneal opacification for the left eye was grade 3, with complete obscuration of iris and pupil details . Corneal staining was diffuse and grade 4 for each eye. Fig. 4 (A) Diffuse white light of the right cornea of patient in case 2 showing regression of central corneal haze at 5 months, (B) 10 months, and (C) 17 months of daily wear of a fluid-ventilating PROSE design with back-surface channels. Fig. 4 Fig. 5 (A) Diffuse white light of the left eye cornea with diffuse corneal neovascularization and haze at baseline for case 2. Progressive regression in corneal haze and neovascularization is visualized at (B) 5 months, (C) 10 months, and (D) 17 months with daily wear of a fluid-ventilating PROSE design with back-surface channels. Fig. 5
3.900391
0.964355
sec[1]/sec[1]/p[1]
en
0.999997
PMC9027328
https://doi.org/10.1016/j.ajoc.2022.101520
[ "corneal", "grade", "cornea", "neovascularization", "haze", "pinhole", "potential", "conjunctiva", "both", "opacification" ]
[ { "code": "9A7Z", "title": "Disorders of the cornea, unspecified" }, { "code": "9A71", "title": "Infectious keratitis" }, { "code": "9A76", "title": "Corneal ulcer" }, { "code": "9A78.4", "title": "Corneal degeneration" }, { "code": "9A70.Z", "title": "Hereditary corneal dystrophies, unspecified" }, { "code": "EH90.Z", "title": "Pressure ulcer of unspecified grade" }, { "code": "EH90.0", "title": "Pressure ulceration grade 1" }, { "code": "GA91.6", "title": "Low grade intraepithelial lesion of prostate" }, { "code": "2E67.22", "title": "High grade squamous intraepithelial lesion of vagina" }, { "code": "EH90.1", "title": "Pressure ulceration grade 2" } ]
=== ICD-11 CODES FOUND === [9A7Z] Disorders of the cornea, unspecified Also known as: Disorders of the cornea, unspecified | corneal disease | disease of cornea | keratopathy [9A71] Infectious keratitis Also known as: Infectious keratitis | corneal inflammation | Bacterial keratitis | Fungal keratitis | fungal infection of cornea [9A76] Corneal ulcer Definition: Loss of epithelial tissue from the surface of the cornea due to progressive erosion and necrosis of the tissue. It is often caused by bacterial, fungal, or viral infection. Also known as: Corneal ulcer | cornea ulcer | ulcerative keratitis | corneal ulcer NOS | Central corneal ulcer Includes: Central corneal ulcer | Ring corneal ulcer | Corneal ulcer with hypopyon [9A78.4] Corneal degeneration Also known as: Corneal degeneration | degenerative corneal opacity | Pellucid marginal degeneration | Arcus senilis | gerontoxon Includes: Arcus senilis Excludes: Mooren ulcer [9A70.Z] Hereditary corneal dystrophies, unspecified Also known as: Hereditary corneal dystrophies, unspecified | Hereditary corneal dystrophies | hereditary corneal dystrophy | corneal dystrophy NOS | familial hereditary corneal degeneration [EH90.Z] Pressure ulcer of unspecified grade Also known as: Pressure ulcer of unspecified grade | Pressure ulceration | pressure injury | pressure ulcer | decubitus ulcer [EH90.0] Pressure ulceration grade 1 Definition: Pressure ulceration grade I is a precursor to skin ulceration. The skin remains intact but there is non-blanchable redness of a localised area, usually over a bony prominence. The area may be painful, firm, soft, warmer or cooler as compared to adjacent tissue. It can be difficult to detect in individuals with dark skin but affected areas may differ in colour from the surrounding skin. The presence of pressure ulceration grade 1 may indicate persons at risk of progressing to frank ulceration. Also known as: Pressure ulceration grade 1 | pressure injury stage 1 | pressure injury stage 1 with nonblanchable erythema | pressure ulcer category 1 | stage I pressure injury Includes: pressure injury stage 1 with nonblanchable erythema [GA91.6] Low grade intraepithelial lesion of prostate Definition: A condition of the prostate, caused by an alteration or mutation in cell growth, or prostatic epithelial cells that are dividing more rapidly than normal epithelium. This condition is characterised by premalignant transformation and abnormal development of the prostatic epithelial tissue. Also known as: Low grade intraepithelial lesion of prostate | Low grade PIN - [prostatic intraepithelial neoplasia] | Low grade prostatic intraepithelial neoplasia | PIN - [prostatic intraepithelial neoplasia] grade 1 to 2 | Low grade dysplasia of prostate Includes: Low grade prostatic intraepithelial neoplasia Excludes: high grade dysplasia of prostate | PIN III | high grade PIN [2E67.22] High grade squamous intraepithelial lesion of vagina Also known as: High grade squamous intraepithelial lesion of vagina | vaginal intraepithelial neoplasia grade II | moderate vaginal dysplasia | vaginal intraepithelial neoplasia grade 2 | VaIN - [vaginal intraepithelial neoplasia] grade 2 [EH90.1] Pressure ulceration grade 2 Definition: Pressure injury with partial thickness loss of dermis. It presents as a shallow open ulcer with a red or pink wound bed without slough or as a serum-filled or serosanguinous blister which may rupture. This category should not be used to describe skin tears, tape burns, incontinence associated dermatitis, maceration or excoriation Also known as: Pressure ulceration grade 2 | bedsore stage II | pressure injury stage 2 | pressure ulcer category 2 | pressure injury stage 2 with partial thickness skin loss Includes: pressure injury stage 2 with partial thickness skin loss === GRAPH WALKS === --- Walk 1 --- [9A7Z] Disorders of the cornea, unspecified --PARENT--> [?] Disorders of the cornea Def: This refers to disorders of the transparent front part of the eye that covers the iris, pupil, and anterior chamber. The cornea, with the anterior chamber and lens, refracts light, with the cornea acc... --CHILD--> [9A72] Traumatic keratitis --- Walk 2 --- [9A7Z] Disorders of the cornea, unspecified --PARENT--> [?] Disorders of the cornea Def: This refers to disorders of the transparent front part of the eye that covers the iris, pupil, and anterior chamber. The cornea, with the anterior chamber and lens, refracts light, with the cornea acc... --CHILD--> [9A70] Hereditary corneal dystrophies Def: The term corneal dystrophy embraces a heterogeneous group of bilateral genetically determined non-inflammatory corneal diseases that are usually restricted to the cornea. The designation is imprecise ... --- Walk 3 --- [9A71] Infectious keratitis --RELATED_TO--> [?] Herpes simplex keratitis Def: This is a viral disease from the herpesviridae family caused by both Herpes simplex virus type 1 (HSV-1) and type 2 (HSV-2). Infection with the herpes virus is categorized into one of several distinct... --PARENT--> [?] Herpes simplex infection of the eye Def: A condition of the eye, caused by an infection with herpes simplex virus type 1 or 2. The condition is characterised by blepharoconjunctivitis or keratitis. Transmission is by direct contact. Confirma... --- Walk 4 --- [9A71] Infectious keratitis --RELATED_TO--> [?] Herpes simplex keratitis Def: This is a viral disease from the herpesviridae family caused by both Herpes simplex virus type 1 (HSV-1) and type 2 (HSV-2). Infection with the herpes virus is categorized into one of several distinct... --CHILD--> [?] Neurotrophic keratopathy --- Walk 5 --- [9A76] Corneal ulcer Def: Loss of epithelial tissue from the surface of the cornea due to progressive erosion and necrosis of the tissue. It is often caused by bacterial, fungal, or viral infection.... --PARENT--> [?] Disorders of the cornea Def: This refers to disorders of the transparent front part of the eye that covers the iris, pupil, and anterior chamber. The cornea, with the anterior chamber and lens, refracts light, with the cornea acc... --CHILD--> [9A72] Traumatic keratitis --- Walk 6 --- [9A76] Corneal ulcer Def: Loss of epithelial tissue from the surface of the cornea due to progressive erosion and necrosis of the tissue. It is often caused by bacterial, fungal, or viral infection.... --PARENT--> [?] Disorders of the cornea Def: This refers to disorders of the transparent front part of the eye that covers the iris, pupil, and anterior chamber. The cornea, with the anterior chamber and lens, refracts light, with the cornea acc... --CHILD--> [9A70] Hereditary corneal dystrophies Def: The term corneal dystrophy embraces a heterogeneous group of bilateral genetically determined non-inflammatory corneal diseases that are usually restricted to the cornea. The designation is imprecise ...
[ "[9A7Z] Disorders of the cornea, unspecified\n --PARENT--> [?] Disorders of the cornea\n Def: This refers to disorders of the transparent front part of the eye that covers the iris, pupil, and anterior chamber. The cornea, with the anterior chamber and lens, refracts light, with the cornea acc...\n --CHILD--> [9A72] Traumatic keratitis", "[9A7Z] Disorders of the cornea, unspecified\n --PARENT--> [?] Disorders of the cornea\n Def: This refers to disorders of the transparent front part of the eye that covers the iris, pupil, and anterior chamber. The cornea, with the anterior chamber and lens, refracts light, with the cornea acc...\n --CHILD--> [9A70] Hereditary corneal dystrophies\n Def: The term corneal dystrophy embraces a heterogeneous group of bilateral genetically determined non-inflammatory corneal diseases that are usually restricted to the cornea. The designation is imprecise ...", "[9A71] Infectious keratitis\n --RELATED_TO--> [?] Herpes simplex keratitis\n Def: This is a viral disease from the herpesviridae family caused by both Herpes simplex virus type 1 (HSV-1) and type 2 (HSV-2). Infection with the herpes virus is categorized into one of several distinct...\n --PARENT--> [?] Herpes simplex infection of the eye\n Def: A condition of the eye, caused by an infection with herpes simplex virus type 1 or 2. The condition is characterised by blepharoconjunctivitis or keratitis. Transmission is by direct contact. Confirma...", "[9A71] Infectious keratitis\n --RELATED_TO--> [?] Herpes simplex keratitis\n Def: This is a viral disease from the herpesviridae family caused by both Herpes simplex virus type 1 (HSV-1) and type 2 (HSV-2). Infection with the herpes virus is categorized into one of several distinct...\n --CHILD--> [?] Neurotrophic keratopathy", "[9A76] Corneal ulcer\n Def: Loss of epithelial tissue from the surface of the cornea due to progressive erosion and necrosis of the tissue. It is often caused by bacterial, fungal, or viral infection....\n --PARENT--> [?] Disorders of the cornea\n Def: This refers to disorders of the transparent front part of the eye that covers the iris, pupil, and anterior chamber. The cornea, with the anterior chamber and lens, refracts light, with the cornea acc...\n --CHILD--> [9A72] Traumatic keratitis", "[9A76] Corneal ulcer\n Def: Loss of epithelial tissue from the surface of the cornea due to progressive erosion and necrosis of the tissue. It is often caused by bacterial, fungal, or viral infection....\n --PARENT--> [?] Disorders of the cornea\n Def: This refers to disorders of the transparent front part of the eye that covers the iris, pupil, and anterior chamber. The cornea, with the anterior chamber and lens, refracts light, with the cornea acc...\n --CHILD--> [9A70] Hereditary corneal dystrophies\n Def: The term corneal dystrophy embraces a heterogeneous group of bilateral genetically determined non-inflammatory corneal diseases that are usually restricted to the cornea. The designation is imprecise ..." ]
9A7Z
Disorders of the cornea, unspecified
[ { "from_icd11": "9A7Z", "icd10_code": "H16203", "icd10_title": "Unspecified keratoconjunctivitis, bilateral" }, { "from_icd11": "9A7Z", "icd10_code": "H16229", "icd10_title": "Keratoconjunctivitis sicca, not specified as Sjogren's, unspecified eye" }, { "from_icd11": "9A7Z", "icd10_code": "H16231", "icd10_title": "Neurotrophic keratoconjunctivitis, right eye" }, { "from_icd11": "9A7Z", "icd10_code": "H16213", "icd10_title": "Exposure keratoconjunctivitis, bilateral" }, { "from_icd11": "9A7Z", "icd10_code": "H16209", "icd10_title": "Unspecified keratoconjunctivitis, unspecified eye" }, { "from_icd11": "9A7Z", "icd10_code": "H16221", "icd10_title": "Keratoconjunctivitis sicca, not specified as Sjogren's, right eye" }, { "from_icd11": "9A7Z", "icd10_code": "H16222", "icd10_title": "Keratoconjunctivitis sicca, not specified as Sjogren's, left eye" }, { "from_icd11": "9A7Z", "icd10_code": "H16202", "icd10_title": "Unspecified keratoconjunctivitis, left eye" }, { "from_icd11": "9A7Z", "icd10_code": "H16299", "icd10_title": "Other keratoconjunctivitis, unspecified eye" }, { "from_icd11": "9A7Z", "icd10_code": "H16292", "icd10_title": "Other keratoconjunctivitis, left eye" }, { "from_icd11": "9A7Z", "icd10_code": "H16219", "icd10_title": "Exposure keratoconjunctivitis, unspecified eye" }, { "from_icd11": "9A7Z", "icd10_code": "H169", "icd10_title": "Unspecified keratitis" }, { "from_icd11": "9A7Z", "icd10_code": "H189", "icd10_title": "Unspecified disorder of cornea" }, { "from_icd11": "9A7Z", "icd10_code": "H168", "icd10_title": "Other keratitis" }, { "from_icd11": "9A7Z", "icd10_code": "H162", "icd10_title": "Keratoconjunctivitis" } ]
H16203
Unspecified keratoconjunctivitis, bilateral
The GARS test recommended KB220PAM (a semi-customized KB220 that offers pro-dopamine regulation by providing a nutraceutical interventional precision complex to balance serotonergic, endorphinergic, glutaminergic, and dopaminergic system restoration). Following this sojourn, the patient has experienced continued improvement as evidenced by the following outcomes: (1) With family collaboration, the patient sought further counsel from the “Mount Sinai Addictive Behavior Program”; (2) Personal coaching focus with a foundation of clarity. Patient began to confront issues including denial, shame, blame, regret, remorse, guilt, hopelessness, helplessness and fear; (3) With the clarity and stabilizing process offered by EFT and pro-dopamine nutrition, the patient progressed to a physician-recommended new step, liberating her from medicinal dependence; (4) With cessation of 95% of medications (with the exception of one stabilizing medicinal agent), along with taking the KB220PAM, the patient confronted and overcame previously unassociated and unaddressed alcohol addiction ; (5) Patient’s awareness, clarity, accountability and personal drive has been clearer than she has ever remembered; (6) Her reliability and willingness to be accountable has created opportunities for transforming relationships in her personal and work life that commonly disintegrate permanently for individuals suffering from addiction.
3.867188
0.930176
sec[4]/p[0]
en
0.999998
PMC9503998
https://doi.org/10.3390/jpm12091416
[ "personal", "clarity", "recommended", "that", "dopamine", "stabilizing", "medicinal", "addiction", "gars", "semi" ]
[ { "code": "6D10.Z", "title": "Personality disorder, severity unspecified" }, { "code": "6B64", "title": "Dissociative identity disorder" }, { "code": "QE50.7", "title": "Personality difficulty" }, { "code": "6D10.2", "title": "Severe personality disorder" }, { "code": "6E68", "title": "Secondary personality change" }, { "code": "8A80.Z", "title": "Migraine, unspecified" }, { "code": "QA76", "title": "Medication or substance that is known to be an allergen without injury or harm" }, { "code": "PL13.6", "title": "Medication or substance that is known to be an allergen, as mode of injury or harm" }, { "code": "9C40.A0", "title": "Papilloedema" }, { "code": "PA6Z", "title": "Unintentional fall from unspecified height" } ]
=== ICD-11 CODES FOUND === [6D10.Z] Personality disorder, severity unspecified Also known as: Personality disorder, severity unspecified | Personality disorder | Specific personality disorders | Enduring personality change after psychiatric illness (deprecated) | Anankastic personality disorder [6B64] Dissociative identity disorder Definition: Dissociative identity disorder is characterised by disruption of identity in which there are two or more distinct personality states (dissociative identities) associated with marked discontinuities in the sense of self and agency. Each personality state includes its own pattern of experiencing, perceiving, conceiving, and relating to self, the body, and the environment. At least two distinct personality states recurrently take executive control of the individual’s consciousness and functioning i Also known as: Dissociative identity disorder | Multiple personality | Multiple personality disorder [QE50.7] Personality difficulty Definition: Personality difficulty refers to pronounced personality characteristics that may affect treatment or health services but do not rise to the level of severity to merit a diagnosis of Personality disorder. Personality difficulty is characterised by long-standing difficulties (e.g., at least 2 years), in the individual’s way of experiencing and thinking about the self, others and the world. In contrast to Personality disorders, these difficulties are manifested in cognitive and emotional experience Also known as: Personality difficulty Excludes: Personality disorder [6D10.2] Severe personality disorder Definition: All general diagnostic requirements for Personality Disorder are met. There are severe disturbances in functioning of the self (e.g., sense of self may be so unstable that individuals report not having a sense of who they are or so rigid that they refuse to participate in any but an extremely narrow range of situations; self view may be characterised by self-contempt or be grandiose or highly eccentric). Problems in interpersonal functioning seriously affect virtually all relationships and the a Also known as: Severe personality disorder | Severe personality disorder with prominent features of negative affectivity | Severe personality disorder with prominent dissocial features | Severe personality disorder with prominent features of disinhibition | Severe personality disorder with prominent anankastic features [6E68] Secondary personality change Definition: A syndrome characterised by a persistent personality disturbance that represents a change from the individual’s previous characteristic personality pattern that is judged to be a direct pathophysiological consequence of a health condition not classified under Mental and behavioural disorders, based on evidence from the history, physical examination, or laboratory findings. The symptoms are not accounted for by delirium or by another mental and behavioural disorder, and are not a psychologically Also known as: Secondary personality change | organic personality disorder | Personality change due to disorders or diseases not classified under mental and behavioural disorders Excludes: Personality difficulty | Personality disorder | Delirium [8A80.Z] Migraine, unspecified Also known as: Migraine, unspecified | Migraine [QA76] Medication or substance that is known to be an allergen without injury or harm Definition: Medication that has previously been identified as an allergen to the patient is administered, but does not result in injury or harm. Also known as: Medication or substance that is known to be an allergen without injury or harm Excludes: Medication or substance that is known to be an allergen, as mode of injury or harm [PL13.6] Medication or substance that is known to be an allergen, as mode of injury or harm Also known as: Medication or substance that is known to be an allergen, as mode of injury or harm | medication error relating to known allergy to drug or substance | adverse drug event relating to known allergy to drug or substance [9C40.A0] Papilloedema Definition: Optic disc swelling that results from increased intracranial pressure Also known as: Papilloedema | Optic disc swelling that results from increased intracranial pressure Includes: Optic disc swelling that results from increased intracranial pressure [PA6Z] Unintentional fall from unspecified height Also known as: Unintentional fall from unspecified height | fall NOS | accidental fall | fall causing injury that resulted in death | fell NOS === GRAPH WALKS === --- Walk 1 --- [6D10.Z] Personality disorder, severity unspecified --PARENT--> [6D10] Personality disorder Def: Personality disorder is characterised by problems in functioning of aspects of the self (e.g., identity, self-worth, accuracy of self-view, self-direction), and/or interpersonal dysfunction (e.g., abi... --PARENT--> [?] Personality disorders and related traits --- Walk 2 --- [6D10.Z] Personality disorder, severity unspecified --PARENT--> [6D10] Personality disorder Def: Personality disorder is characterised by problems in functioning of aspects of the self (e.g., identity, self-worth, accuracy of self-view, self-direction), and/or interpersonal dysfunction (e.g., abi... --CHILD--> [6D10.0] Mild personality disorder Def: All general diagnostic requirements for Personality Disorder are met. Disturbances affect some areas of personality functioning but not others (e.g., problems with self-direction in the absence of pro... --- Walk 3 --- [6B64] Dissociative identity disorder Def: Dissociative identity disorder is characterised by disruption of identity in which there are two or more distinct personality states (dissociative identities) associated with marked discontinuities in... --PARENT--> [?] Dissociative disorders Def: Dissociative disorders are characterised by involuntary disruption or discontinuity in the normal integration of one or more of the following: identity, sensations, perceptions, affects, thoughts, mem... --RELATED_TO--> [?] Secondary dissociative syndrome Def: A syndrome characterised by the presence of prominent dissociative symptoms (e.g., depersonalization, derealization) that is judged to be the direct pathophysiological consequence of a health conditio... --- Walk 4 --- [6B64] Dissociative identity disorder Def: Dissociative identity disorder is characterised by disruption of identity in which there are two or more distinct personality states (dissociative identities) associated with marked discontinuities in... --PARENT--> [?] Dissociative disorders Def: Dissociative disorders are characterised by involuntary disruption or discontinuity in the normal integration of one or more of the following: identity, sensations, perceptions, affects, thoughts, mem... --PARENT--> [06] Mental, behavioural or neurodevelopmental disorders Def: Mental, behavioural and neurodevelopmental disorders are syndromes characterised by clinically significant disturbance in an individual's cognition, emotional regulation, or behaviour that reflects a ... --- Walk 5 --- [QE50.7] Personality difficulty Def: Personality difficulty refers to pronounced personality characteristics that may affect treatment or health services but do not rise to the level of severity to merit a diagnosis of Personality disord... --PARENT--> [QE50] Problem associated with interpersonal interactions --CHILD--> [QE50.1] Relationships with teachers or classmates --- Walk 6 --- [QE50.7] Personality difficulty Def: Personality difficulty refers to pronounced personality characteristics that may affect treatment or health services but do not rise to the level of severity to merit a diagnosis of Personality disord... --EXCLUDES--> [?] Personality disorder Def: Personality disorder is characterised by problems in functioning of aspects of the self (e.g., identity, self-worth, accuracy of self-view, self-direction), and/or interpersonal dysfunction (e.g., abi... --CHILD--> [?] Moderate personality disorder Def: All general diagnostic requirements for Personality Disorder are met. Disturbances affect multiple areas of personality functioning (e.g., identity or sense of self, ability to form intimate relations...
[ "[6D10.Z] Personality disorder, severity unspecified\n --PARENT--> [6D10] Personality disorder\n Def: Personality disorder is characterised by problems in functioning of aspects of the self (e.g., identity, self-worth, accuracy of self-view, self-direction), and/or interpersonal dysfunction (e.g., abi...\n --PARENT--> [?] Personality disorders and related traits", "[6D10.Z] Personality disorder, severity unspecified\n --PARENT--> [6D10] Personality disorder\n Def: Personality disorder is characterised by problems in functioning of aspects of the self (e.g., identity, self-worth, accuracy of self-view, self-direction), and/or interpersonal dysfunction (e.g., abi...\n --CHILD--> [6D10.0] Mild personality disorder\n Def: All general diagnostic requirements for Personality Disorder are met. Disturbances affect some areas of personality functioning but not others (e.g., problems with self-direction in the absence of pro...", "[6B64] Dissociative identity disorder\n Def: Dissociative identity disorder is characterised by disruption of identity in which there are two or more distinct personality states (dissociative identities) associated with marked discontinuities in...\n --PARENT--> [?] Dissociative disorders\n Def: Dissociative disorders are characterised by involuntary disruption or discontinuity in the normal integration of one or more of the following: identity, sensations, perceptions, affects, thoughts, mem...\n --RELATED_TO--> [?] Secondary dissociative syndrome\n Def: A syndrome characterised by the presence of prominent dissociative symptoms (e.g., depersonalization, derealization) that is judged to be the direct pathophysiological consequence of a health conditio...", "[6B64] Dissociative identity disorder\n Def: Dissociative identity disorder is characterised by disruption of identity in which there are two or more distinct personality states (dissociative identities) associated with marked discontinuities in...\n --PARENT--> [?] Dissociative disorders\n Def: Dissociative disorders are characterised by involuntary disruption or discontinuity in the normal integration of one or more of the following: identity, sensations, perceptions, affects, thoughts, mem...\n --PARENT--> [06] Mental, behavioural or neurodevelopmental disorders\n Def: Mental, behavioural and neurodevelopmental disorders are syndromes characterised by clinically significant disturbance in an individual's cognition, emotional regulation, or behaviour that reflects a ...", "[QE50.7] Personality difficulty\n Def: Personality difficulty refers to pronounced personality characteristics that may affect treatment or health services but do not rise to the level of severity to merit a diagnosis of Personality disord...\n --PARENT--> [QE50] Problem associated with interpersonal interactions\n --CHILD--> [QE50.1] Relationships with teachers or classmates", "[QE50.7] Personality difficulty\n Def: Personality difficulty refers to pronounced personality characteristics that may affect treatment or health services but do not rise to the level of severity to merit a diagnosis of Personality disord...\n --EXCLUDES--> [?] Personality disorder\n Def: Personality disorder is characterised by problems in functioning of aspects of the self (e.g., identity, self-worth, accuracy of self-view, self-direction), and/or interpersonal dysfunction (e.g., abi...\n --CHILD--> [?] Moderate personality disorder\n Def: All general diagnostic requirements for Personality Disorder are met. Disturbances affect multiple areas of personality functioning (e.g., identity or sense of self, ability to form intimate relations..." ]
6D10.Z
Personality disorder, severity unspecified
[ { "from_icd11": "6D10.Z", "icd10_code": "F6089", "icd10_title": "Other specific personality disorders" }, { "from_icd11": "6D10.Z", "icd10_code": "F6081", "icd10_title": "Narcissistic personality disorder" }, { "from_icd11": "6D10.Z", "icd10_code": "F603", "icd10_title": "Borderline personality disorder" }, { "from_icd11": "6D10.Z", "icd10_code": "F602", "icd10_title": "Antisocial personality disorder" }, { "from_icd11": "6D10.Z", "icd10_code": "F609", "icd10_title": "Personality disorder, unspecified" }, { "from_icd11": "6D10.Z", "icd10_code": "F600", "icd10_title": "Paranoid personality disorder" }, { "from_icd11": "6D10.Z", "icd10_code": "F606", "icd10_title": "Avoidant personality disorder" }, { "from_icd11": "6D10.Z", "icd10_code": "F601", "icd10_title": "Schizoid personality disorder" }, { "from_icd11": "6D10.Z", "icd10_code": "F69", "icd10_title": "Unspecified disorder of adult personality and behavior" }, { "from_icd11": "6D10.Z", "icd10_code": "F607", "icd10_title": "Dependent personality disorder" }, { "from_icd11": "6D10.Z", "icd10_code": "F604", "icd10_title": "Histrionic personality disorder" }, { "from_icd11": "6D10.Z", "icd10_code": "F60-F69", "icd10_title": "" }, { "from_icd11": "6D10.Z", "icd10_code": "F60", "icd10_title": "Specific personality disorders" }, { "from_icd11": "6D10.Z", "icd10_code": "F608", "icd10_title": "Other specific personality disorders" }, { "from_icd11": "6D10.Z", "icd10_code": "F61", "icd10_title": "" } ]
F6089
Other specific personality disorders
A 29-year-old male carpenter initially presented to the referring facility with a 4-year history of recurrent vertigo and syncope with right rotation and extension of the neck. Computed tomography (CT)-scan and magnetic resonance imaging (MRI)-scan 2 years prior revealed a dominant right VA, with an aberrant course. The right VA traversed anterior to an enlarged C6 tubercle of the transverse process, between longus colli and longus capitis muscles at levels C4-5, and entered the foramen transversarium at C4 . The left VA was hypoplastic, and there were no significant posterior communicating arteries. Digital substraction angiography (DSA) demonstrated positional complete right VA occlusion at level C6. This was felt to be secondary to compression between the longus colli and the longus capitis muscles against an enlarged anterior C6 tubercle of the transverse process . He underwent a surgical decompression of the right VA at levels C5-C6 with removal of the enlarged anterior tubercle of C6. This was performed with intraoperative catheter angiography to confirm adequate free mobilization. The procedure was complicated by temporary post-operative dysphagia, and permanent mild Horner’s syndrome. Post-operatively, while his positional VBI symptoms improved, they persisted. He was managed conservatively and counseled to avoid extreme neck rotation and low dose aspirin was prescribed to prevent stroke.
4.003906
0.979004
sec[1]/sec[0]/p[0]
en
0.999997
35152775
https://doi.org/10.1177/00034894221077477
[ "longus", "enlarged", "tubercle", "rotation", "neck", "scan", "transverse", "process", "colli", "capitis" ]
[ { "code": "ME10.00", "title": "Hepatomegaly, not elsewhere classified" }, { "code": "GA16.Y", "title": "Other specified acquired abnormalities of uterus, except cervix" }, { "code": "ME10.01", "title": "Splenomegaly, not elsewhere classified" }, { "code": "DA03.Y", "title": "Other specified diseases of tongue" }, { "code": "LA11.1", "title": "Structural developmental anomalies of cornea" }, { "code": "1B10.Z", "title": "Respiratory tuberculosis, without mention of bacteriological or histological confirmation" }, { "code": "FB82.1", "title": "Osteochondrosis or osteochondritis dissecans" }, { "code": "1B21.Z", "title": "Non-tuberculous mycobacterial infection of unspecified site" }, { "code": "1B10.0", "title": "Respiratory tuberculosis, confirmed" }, { "code": "FB53.1", "title": "Rotator cuff syndrome" } ]
=== ICD-11 CODES FOUND === [ME10.00] Hepatomegaly, not elsewhere classified Also known as: Hepatomegaly, not elsewhere classified | enlarged liver | enlargement of liver | Hepatomegaly NOS | acute hepatomegaly [GA16.Y] Other specified acquired abnormalities of uterus, except cervix Also known as: Other specified acquired abnormalities of uterus, except cervix | Polyp of corpus uteri | intrauterine polyp | polyp of body of uterus | polyp of uterus [ME10.01] Splenomegaly, not elsewhere classified Definition: This refers to swelling of the spleen beyond its normal size, not elsewhere described. Also known as: Splenomegaly, not elsewhere classified | splenomegalia | Splenomegaly NOS | spleen palpable | enlarged spleen NOS Excludes: Hypersplenism [DA03.Y] Other specified diseases of tongue Also known as: Other specified diseases of tongue | Crenated tongue | Glossoplegia | Hemiatrophy of tongue | Thickening of tongue [LA11.1] Structural developmental anomalies of cornea Definition: Any condition caused by failure of the cornea to correctly develop during the antenatal period. Also known as: Structural developmental anomalies of cornea | Malformations of cornea | Cornea plana | Flat cornea | Cornea plana, unilateral [1B10.Z] Respiratory tuberculosis, without mention of bacteriological or histological confirmation Also known as: Respiratory tuberculosis, without mention of bacteriological or histological confirmation | Tuberculosis of the respiratory system | respiratory tuberculosis | pulmonary tuberculosis | pulmonary TB [FB82.1] Osteochondrosis or osteochondritis dissecans Definition: Note: Osteochondroses are typically referred to by eponyms. The most common eponyms are indexed to osteochondrosis with specification identified by the site and time in life. Also known as: Osteochondrosis or osteochondritis dissecans | osteochondral lesion | Osteochondrosis not specified as adult or juvenile, of unspecified site | osteochondrosis NOS | Juvenile osteochondrosis [1B21.Z] Non-tuberculous mycobacterial infection of unspecified site Also known as: Non-tuberculous mycobacterial infection of unspecified site | Infections due to non-tuberculous mycobacteria | infection due to other mycobacteria | Non-tuberculous mycobacterial infections | MOTT - [mycobacteria other than tubercle bacilli] [1B10.0] Respiratory tuberculosis, confirmed Definition: A disease of the respiratory tract, caused by an infection with the bacteria Mycobacterium tuberculosis, which has been confirmed by laboratory testing. This disease is characterised by chronic cough, and sputum production that may be haemorrhagic. Transmission is commonly by inhalation of infected respiratory secretions. Confirmation is by identification of Mycobacterium tuberculosis in clinical samples. Also known as: Respiratory tuberculosis, confirmed | respiratory tuberculosis, with bacteriological or histological confirmation | tuberculosis of chest, with bacteriological or histological confirmation | Tuberculosis of lung, confirmed by sputum microscopy with or without culture | pulmonary tuberculosis confirmed by sputum microscopy with or without culture [FB53.1] Rotator cuff syndrome Also known as: Rotator cuff syndrome | impingement syndrome | rotator cuff rupture | rotator cuff tear | rupture of rotator cuff of shoulder Excludes: Rotator cuff tendonitis === GRAPH WALKS === --- Walk 1 --- [ME10.00] Hepatomegaly, not elsewhere classified --PARENT--> [ME10.0] Hepatomegaly or splenomegaly Def: Hepatomegaly is swelling of the liver beyond its normal size and splenomegaly is an enlargement of the spleen beyond its normal size.... --CHILD--> [ME10.00] Hepatomegaly, not elsewhere classified --- Walk 2 --- [ME10.00] Hepatomegaly, not elsewhere classified --PARENT--> [ME10.0] Hepatomegaly or splenomegaly Def: Hepatomegaly is swelling of the liver beyond its normal size and splenomegaly is an enlargement of the spleen beyond its normal size.... --CHILD--> [ME10.02] Hepatomegaly with splenomegaly Def: This refers to swelling of the liver and spleen beyond its normal size, not elsewhere described.... --- Walk 3 --- [GA16.Y] Other specified acquired abnormalities of uterus, except cervix --PARENT--> [GA16] Acquired abnormalities of uterus, except cervix Def: Any condition of the uterus, caused by determinants arising after birth. These conditions are characterised by a malfunction, malformation, or another anomaly of the uterus (excluding the cervix).... --RELATED_TO--> [?] Leiomyoma of uterus Def: A well-circumscribed benign smooth muscle neoplasm of uterus characterised by the presence of spindle cells with cigar-shaped nuclei, interlacing fascicles, and a whorled pattern.... --- Walk 4 --- [GA16.Y] Other specified acquired abnormalities of uterus, except cervix --PARENT--> [GA16] Acquired abnormalities of uterus, except cervix Def: Any condition of the uterus, caused by determinants arising after birth. These conditions are characterised by a malfunction, malformation, or another anomaly of the uterus (excluding the cervix).... --CHILD--> [GA16.1] Malposition of uterus Def: A condition of the uterus, caused by weakened pelvic ligaments, enlargement of the uterus, scarred pelvic tissue from pregnancy, tumour, menopause, endometriosis, inflammation, or salpingitis. This co... --- Walk 5 --- [ME10.01] Splenomegaly, not elsewhere classified Def: This refers to swelling of the spleen beyond its normal size, not elsewhere described.... --EXCLUDES--> [?] Hypersplenism Def: A disease caused by determinants such as cirrhosis, malaria, tuberculosis or inflammatory disorders leading overactive spleen function. This disease is characterised by the presence of an enlarged spl... --EXCLUDES--> [?] Splenomegaly, not elsewhere classified Def: This refers to swelling of the spleen beyond its normal size, not elsewhere described.... --- Walk 6 --- [ME10.01] Splenomegaly, not elsewhere classified Def: This refers to swelling of the spleen beyond its normal size, not elsewhere described.... --EXCLUDES--> [?] Hypersplenism Def: A disease caused by determinants such as cirrhosis, malaria, tuberculosis or inflammatory disorders leading overactive spleen function. This disease is characterised by the presence of an enlarged spl... --EXCLUDES--> [?] Structural developmental anomalies of spleen Def: Any condition caused by failure of the spleen to correctly develop during the antenatal period....
[ "[ME10.00] Hepatomegaly, not elsewhere classified\n --PARENT--> [ME10.0] Hepatomegaly or splenomegaly\n Def: Hepatomegaly is swelling of the liver beyond its normal size and splenomegaly is an enlargement of the spleen beyond its normal size....\n --CHILD--> [ME10.00] Hepatomegaly, not elsewhere classified", "[ME10.00] Hepatomegaly, not elsewhere classified\n --PARENT--> [ME10.0] Hepatomegaly or splenomegaly\n Def: Hepatomegaly is swelling of the liver beyond its normal size and splenomegaly is an enlargement of the spleen beyond its normal size....\n --CHILD--> [ME10.02] Hepatomegaly with splenomegaly\n Def: This refers to swelling of the liver and spleen beyond its normal size, not elsewhere described....", "[GA16.Y] Other specified acquired abnormalities of uterus, except cervix\n --PARENT--> [GA16] Acquired abnormalities of uterus, except cervix\n Def: Any condition of the uterus, caused by determinants arising after birth. These conditions are characterised by a malfunction, malformation, or another anomaly of the uterus (excluding the cervix)....\n --RELATED_TO--> [?] Leiomyoma of uterus\n Def: A well-circumscribed benign smooth muscle neoplasm of uterus characterised by the presence of spindle cells with cigar-shaped nuclei, interlacing fascicles, and a whorled pattern....", "[GA16.Y] Other specified acquired abnormalities of uterus, except cervix\n --PARENT--> [GA16] Acquired abnormalities of uterus, except cervix\n Def: Any condition of the uterus, caused by determinants arising after birth. These conditions are characterised by a malfunction, malformation, or another anomaly of the uterus (excluding the cervix)....\n --CHILD--> [GA16.1] Malposition of uterus\n Def: A condition of the uterus, caused by weakened pelvic ligaments, enlargement of the uterus, scarred pelvic tissue from pregnancy, tumour, menopause, endometriosis, inflammation, or salpingitis. This co...", "[ME10.01] Splenomegaly, not elsewhere classified\n Def: This refers to swelling of the spleen beyond its normal size, not elsewhere described....\n --EXCLUDES--> [?] Hypersplenism\n Def: A disease caused by determinants such as cirrhosis, malaria, tuberculosis or inflammatory disorders leading overactive spleen function. This disease is characterised by the presence of an enlarged spl...\n --EXCLUDES--> [?] Splenomegaly, not elsewhere classified\n Def: This refers to swelling of the spleen beyond its normal size, not elsewhere described....", "[ME10.01] Splenomegaly, not elsewhere classified\n Def: This refers to swelling of the spleen beyond its normal size, not elsewhere described....\n --EXCLUDES--> [?] Hypersplenism\n Def: A disease caused by determinants such as cirrhosis, malaria, tuberculosis or inflammatory disorders leading overactive spleen function. This disease is characterised by the presence of an enlarged spl...\n --EXCLUDES--> [?] Structural developmental anomalies of spleen\n Def: Any condition caused by failure of the spleen to correctly develop during the antenatal period...." ]
ME10.00
Hepatomegaly, not elsewhere classified
[ { "from_icd11": "ME10.00", "icd10_code": "R160", "icd10_title": "Hepatomegaly, not elsewhere classified" }, { "from_icd11": "ME10.01", "icd10_code": "R161", "icd10_title": "Splenomegaly, not elsewhere classified" }, { "from_icd11": "1B10.Z", "icd10_code": "A162", "icd10_title": "" }, { "from_icd11": "1B10.Z", "icd10_code": "A163", "icd10_title": "" }, { "from_icd11": "1B10.Z", "icd10_code": "A164", "icd10_title": "" }, { "from_icd11": "1B10.Z", "icd10_code": "A165", "icd10_title": "" }, { "from_icd11": "1B10.Z", "icd10_code": "A167", "icd10_title": "" }, { "from_icd11": "1B10.Z", "icd10_code": "A168", "icd10_title": "" }, { "from_icd11": "1B10.Z", "icd10_code": "A169", "icd10_title": "" }, { "from_icd11": "FB82.1", "icd10_code": "M9262", "icd10_title": "Juvenile osteochondrosis of tarsus, left ankle" }, { "from_icd11": "FB82.1", "icd10_code": "M9320", "icd10_title": "Osteochondritis dissecans of unspecified site" }, { "from_icd11": "FB82.1", "icd10_code": "M9261", "icd10_title": "Juvenile osteochondrosis of tarsus, right ankle" }, { "from_icd11": "FB82.1", "icd10_code": "M9250", "icd10_title": "Juvenile osteochondrosis of tibia and fibula, unspecified leg" }, { "from_icd11": "FB82.1", "icd10_code": "M4200", "icd10_title": "Juvenile osteochondrosis of spine, site unspecified" }, { "from_icd11": "FB82.1", "icd10_code": "M9112", "icd10_title": "Juvenile osteochondrosis of head of femur [Legg-Calve-Perthes], left leg" } ]
R160
Hepatomegaly, not elsewhere classified
The term “movement disorder” denotes abnormality in movement, which may be either voluntary or involuntary . There are various movement disorders: dystonia, tremor, myoclonus, tardive dyskinesia, hemiballismus, tics, chorea, athetosis, and others . Multiple etiologies of movement disorders include genetics, toxins, metabolic abnormalities, infections, strokes, and vascular complications . Among them, drug-induced dyskinesia is one of the leading causes of movement disorder . In a constantly changing population using widespread polypharmacy, identifying the combination of drugs that can cause tremors is very important to generate risk profiles for individual patients . The drugs implicated in movement disorder are antipsychotics, CNS stimulants, antidepressants, anticonvulsants, antiparkinsonian drugs, bronchodilators, amiodarone, and lithium . However, a combination of skeletal muscle relaxants and second-generation antipsychotics such as baclofen and clozapine-induced movement disorder, especially dyskinesia, is a rare incident . Risk factors for drug-induced movement disorder include polypharmacy, male sex, older age, an increased dose of medicine, and extended-release drug formulations that quickly reach high toxic levels in the body . Herein, we present a case report of a 69-year-old male who presented with clozapine and baclofen-induced dyskinesia, a rare adverse effect of these medications.
4.242188
0.927734
sec[0]/p[0]
en
0.999995
PMC9203264
https://doi.org/10.7759/cureus.25068
[ "movement", "dyskinesia", "induced", "drug", "drugs", "disorders", "include", "polypharmacy", "combination", "that" ]
[ { "code": "8A0Z", "title": "Movement disorders, unspecified" }, { "code": "8A0Y", "title": "Other specified movement disorders" }, { "code": "6B60.8Y", "title": "Dissociative neurological symptom disorder, with other specified movement disturbance" }, { "code": "8A07", "title": "Certain specified movement disorder" }, { "code": "8D43.4", "title": "Movement disorders due to toxicity" }, { "code": "MB47.4", "title": "Dystonia" }, { "code": "8A02.2", "title": "Paroxysmal dystonia" }, { "code": "CB40.0", "title": "Ciliary dyskinesia" }, { "code": "DA21.Z", "title": "Motility disorders of oesophagus, unspecified" }, { "code": "8A02.0Z", "title": "Primary dystonia, unspecified" } ]
=== ICD-11 CODES FOUND === [8A0Z] Movement disorders, unspecified Also known as: Movement disorders, unspecified | extrapyramidal and movement disorders | abnormal movement NOS | disorder of basal ganglia | basal ganglia disease [8A0Y] Other specified movement disorders Also known as: Other specified movement disorders | Other movement disorders, not elsewhere classified | chorea NOS | Familial congenital mirror movements | Primary progressive freezing gait [6B60.8Y] Dissociative neurological symptom disorder, with other specified movement disturbance Also known as: Dissociative neurological symptom disorder, with other specified movement disturbance | Functional movement disorder | Other functional hyperkinetic movements [8A07] Certain specified movement disorder Definition: Neurologic motor disorders that present with slowness of movement (bradykinesia or hypokinesia) or abnormal involuntary movements (hyperkinesias) as a result of genetic, infectious, toxic, metabolic, inflammatory, or vascular abnormalities. Also known as: Certain specified movement disorder [8D43.4] Movement disorders due to toxicity Definition: Movements of the body such as hyperkinesias, dyskinesias, myoclonus, chorea, tremor and tics produced by toxicity either by toxin or drug, e.g. toxicity by manganese, neuroleptic drugs, calcium channel blockers, gastrointestinal prokinetics, antiarrhythmics and antidepressants that may induce Parkinsonism. Also known as: Movement disorders due to toxicity [MB47.4] Dystonia Definition: Sustained muscle contraction, involuntary movements that can lead to fixed abnormal postures Also known as: Dystonia | dystonia disorder | Dyskinesia NOS | dyskinetic [8A02.2] Paroxysmal dystonia Definition: Paroxysmal dyskinesias are a group of rare movement disorders characterised by their recurrent and episodic nature, arising from a background of normal motor activity and behaviour. These abnormal movements can manifest in the form of ballism, dystonia, chorea and athetosis or a combination of these. Also known as: Paroxysmal dystonia | Paroxysmal Dyskinesia | PxD - [paroxysmal dyskinesia] | Paroxysmal kinesigenic dyskinesia | paroxysmal kinesigenic dystonia [CB40.0] Ciliary dyskinesia Definition: Defective function of the cilia lining the respiratory tract (lower and upper, sinuses, Eustachian tube, middle ear) resulting in altered mucociliary transport and manifesting as recurrent upper and lower respiratory infection, chronic productive cough, chronic rhinosinusitis or persistent otitis media. Acquired forms result from respiratory tract injury associated especially with respiratory infections such as bronchiolitis or chronic obstructive pulmonary disease. The rare primary forms are in Also known as: Ciliary dyskinesia | Secondary ciliary dyskinesia | Acquired ciliary dyskinesia [DA21.Z] Motility disorders of oesophagus, unspecified Also known as: Motility disorders of oesophagus, unspecified | Motility disorders of oesophagus | Dyskinesia of oesophagus | oesophageal dysmotility | oesophageal motility disorder [8A02.0Z] Primary dystonia, unspecified Also known as: Primary dystonia, unspecified | Primary dystonia | neuroleptic dyskinesia === GRAPH WALKS === --- Walk 1 --- [8A0Z] Movement disorders, unspecified --PARENT--> [?] Movement disorders Def: This is a group of involuntary movement disorders.... --RELATED_TO--> [?] Periodic limb movement disorder Def: Periodic limb movement disorder is characterised by periodic episodes of repetitive (> 5/hour in children or > 15/hour in adults), highly stereotyped limb movements that occur during sleep, in conjunc... --- Walk 2 --- [8A0Z] Movement disorders, unspecified --PARENT--> [?] Movement disorders Def: This is a group of involuntary movement disorders.... --RELATED_TO--> [?] Restless legs syndrome Def: Restless legs syndrome is a waking sensorimotor disorder characterised by a complaint of a strong, nearly irresistible urge to move the limbs. This urge to move is often but not always accompanied by ... --- Walk 3 --- [8A0Y] Other specified movement disorders --PARENT--> [?] Movement disorders Def: This is a group of involuntary movement disorders.... --RELATED_TO--> [?] Hemifacial spasm Def: Hemifacial spasm (HFS) is a movement disorder most commonly caused by vascular compression of the VII cranial nerve at its root exit zone from the brainstem. It manifests as involuntary contractions a... --- Walk 4 --- [8A0Y] Other specified movement disorders --PARENT--> [?] Movement disorders Def: This is a group of involuntary movement disorders.... --CHILD--> [8A02] Dystonic disorders --- Walk 5 --- [6B60.8Y] Dissociative neurological symptom disorder, with other specified movement disturbance --PARENT--> [6B60.8] Dissociative neurological symptom disorder, with movement disturbance Def: Dissociative neurological symptom disorder, with movement disturbance is characterised by symptoms such as chorea, myoclonus, tremor, dystonia, facial spasm, parkinsonism, or dyskinesia that are not c... --CHILD--> [6B60.82] Dissociative neurological symptom disorder, with tremor Def: Dissociative neurological symptom disorder, with tremor is characterised by involuntary oscillation of a body part that is not consistent with a recognised disease of the nervous system, other mental,... --- Walk 6 --- [6B60.8Y] Dissociative neurological symptom disorder, with other specified movement disturbance --PARENT--> [6B60.8] Dissociative neurological symptom disorder, with movement disturbance Def: Dissociative neurological symptom disorder, with movement disturbance is characterised by symptoms such as chorea, myoclonus, tremor, dystonia, facial spasm, parkinsonism, or dyskinesia that are not c... --CHILD--> [6B60.80] Dissociative neurological symptom disorder, with chorea Def: Dissociative neurological symptom disorder, with chorea is characterised by irregular, non-repetitive, brief, jerky, flowing movements that move randomly from one part of the body to another that are ...
[ "[8A0Z] Movement disorders, unspecified\n --PARENT--> [?] Movement disorders\n Def: This is a group of involuntary movement disorders....\n --RELATED_TO--> [?] Periodic limb movement disorder\n Def: Periodic limb movement disorder is characterised by periodic episodes of repetitive (> 5/hour in children or > 15/hour in adults), highly stereotyped limb movements that occur during sleep, in conjunc...", "[8A0Z] Movement disorders, unspecified\n --PARENT--> [?] Movement disorders\n Def: This is a group of involuntary movement disorders....\n --RELATED_TO--> [?] Restless legs syndrome\n Def: Restless legs syndrome is a waking sensorimotor disorder characterised by a complaint of a strong, nearly irresistible urge to move the limbs. This urge to move is often but not always accompanied by ...", "[8A0Y] Other specified movement disorders\n --PARENT--> [?] Movement disorders\n Def: This is a group of involuntary movement disorders....\n --RELATED_TO--> [?] Hemifacial spasm\n Def: Hemifacial spasm (HFS) is a movement disorder most commonly caused by vascular compression of the VII cranial nerve at its root exit zone from the brainstem. It manifests as involuntary contractions a...", "[8A0Y] Other specified movement disorders\n --PARENT--> [?] Movement disorders\n Def: This is a group of involuntary movement disorders....\n --CHILD--> [8A02] Dystonic disorders", "[6B60.8Y] Dissociative neurological symptom disorder, with other specified movement disturbance\n --PARENT--> [6B60.8] Dissociative neurological symptom disorder, with movement disturbance\n Def: Dissociative neurological symptom disorder, with movement disturbance is characterised by symptoms such as chorea, myoclonus, tremor, dystonia, facial spasm, parkinsonism, or dyskinesia that are not c...\n --CHILD--> [6B60.82] Dissociative neurological symptom disorder, with tremor\n Def: Dissociative neurological symptom disorder, with tremor is characterised by involuntary oscillation of a body part that is not consistent with a recognised disease of the nervous system, other mental,...", "[6B60.8Y] Dissociative neurological symptom disorder, with other specified movement disturbance\n --PARENT--> [6B60.8] Dissociative neurological symptom disorder, with movement disturbance\n Def: Dissociative neurological symptom disorder, with movement disturbance is characterised by symptoms such as chorea, myoclonus, tremor, dystonia, facial spasm, parkinsonism, or dyskinesia that are not c...\n --CHILD--> [6B60.80] Dissociative neurological symptom disorder, with chorea\n Def: Dissociative neurological symptom disorder, with chorea is characterised by irregular, non-repetitive, brief, jerky, flowing movements that move randomly from one part of the body to another that are ..." ]
8A0Z
Movement disorders, unspecified
[ { "from_icd11": "8A0Z", "icd10_code": "G2571", "icd10_title": "Drug induced akathisia" }, { "from_icd11": "8A0Z", "icd10_code": "G2579", "icd10_title": "Other drug induced movement disorders" }, { "from_icd11": "8A0Z", "icd10_code": "G2570", "icd10_title": "Drug induced movement disorder, unspecified" }, { "from_icd11": "8A0Z", "icd10_code": "G2581", "icd10_title": "Restless legs syndrome" }, { "from_icd11": "8A0Z", "icd10_code": "R2681", "icd10_title": "Unsteadiness on feet" }, { "from_icd11": "8A0Z", "icd10_code": "G3109", "icd10_title": "Other frontotemporal dementia" }, { "from_icd11": "8A0Z", "icd10_code": "G2589", "icd10_title": "Other specified extrapyramidal and movement disorders" }, { "from_icd11": "8A0Z", "icd10_code": "G3101", "icd10_title": "Pick's disease" }, { "from_icd11": "8A0Z", "icd10_code": "G2582", "icd10_title": "Stiff-man syndrome" }, { "from_icd11": "8A0Z", "icd10_code": "G20", "icd10_title": "Parkinson's disease" }, { "from_icd11": "8A0Z", "icd10_code": "G255", "icd10_title": "Other chorea" }, { "from_icd11": "8A0Z", "icd10_code": "G210", "icd10_title": "Malignant neuroleptic syndrome" }, { "from_icd11": "8A0Z", "icd10_code": "G111", "icd10_title": "Early-onset cerebellar ataxia" }, { "from_icd11": "8A0Z", "icd10_code": "G259", "icd10_title": "Extrapyramidal and movement disorder, unspecified" }, { "from_icd11": "8A0Z", "icd10_code": "R268", "icd10_title": "Other abnormalities of gait and mobility" } ]
G2571
Drug induced akathisia
Our patient presented with only bilateral prelingual sensorineural hearing loss without any other signs or symptoms of the central nervous system or muscle involvement (e.g., seizures, dementia, hypotonia, paralysis) that would typically be found in COXPD24. Furthermore, head and neck CT and MRI scans revealed no abnormal findings indicative of NARS2-associated syndromes such as Alpers or Leigh syndrome. Laboratory tests did not show significant findings and, apart from delayed language development, cognitive and motor development milestones were otherwise within reference ranges. This presentation resembles the only known report of nonsyndromic hearing loss occurring due to a NARS2 mutation, labeled autosomal recessive deafness 94 (DFNB94). In 2015, Simon et al. described a consanguineous family in which five adult members possessed a homozygous missense mutation and had nonsyndromic hearing loss without any other clinical characteristics, apart from possible premature menopause in two family members; thus, the designation of DFNB94 was given . Other mt-aaRS mutations may also cause hearing loss, whether nonsyndromic or associated with specific syndromes. For example, mutations in the KARS gene can cause nonsyndromic autosomal recessive deafness 89 (DFNB89), while mutations in the LARS2 or HARS2 genes can cause Perrault syndrome, a disorder of sensorineural hearing loss and ovarian dysfunction .
4.355469
0.766113
sec[2]/p[2]
en
0.999996
PMC9748626
https://doi.org/10.7759/cureus.31467
[ "hearing", "loss", "nonsyndromic", "mutations", "cause", "sensorineural", "without", "associated", "syndromes", "apart" ]
[ { "code": "AB52", "title": "Deafness not otherwise specified" }, { "code": "QA00.7", "title": "Examination of ears and hearing" }, { "code": "MC4Y", "title": "Other specified symptoms or signs involving the ear or mastoid process" }, { "code": "AB54", "title": "Presbycusis" }, { "code": "AB5Z", "title": "Disorders with hearing impairment, unspecified" }, { "code": "FB32.Y", "title": "Other specified disorders of muscles" }, { "code": "QE61.0", "title": "Loss or death of child" }, { "code": "5C70.0", "title": "Dehydration" }, { "code": "MB27.Z", "title": "Symptoms or signs of perceptual disturbance, unspecified" }, { "code": "MG43.5", "title": "Excessive weight loss" } ]
=== ICD-11 CODES FOUND === [AB52] Deafness not otherwise specified Also known as: Deafness not otherwise specified | deaf | hearing loss NOS | hearing impairment | hearing loss [QA00.7] Examination of ears and hearing Also known as: Examination of ears and hearing | examination of ear | hearing examination | hearing test [MC4Y] Other specified symptoms or signs involving the ear or mastoid process Also known as: Other specified symptoms or signs involving the ear or mastoid process | Hearing complaint | Fear of ear disease [AB54] Presbycusis Definition: The term presbycusis refers to sensorineural hearing impairment in elderly individuals. Characteristically, presbycusis involves bilateral high-frequency hearing loss associated with difficulty in speech discrimination and central auditory processing of information. Also known as: Presbycusis | Presbyacusia | age-related hearing loss | senile deafness | hard of hearing Includes: Presbyacusia [AB5Z] Disorders with hearing impairment, unspecified Also known as: Disorders with hearing impairment, unspecified | disorders with hearing loss [FB32.Y] Other specified disorders of muscles Also known as: Other specified disorders of muscles | Muscle wasting or atrophy, not elsewhere classified | muscle wasting | muscle wasting disorder | Sarcopenia [QE61.0] Loss or death of child Also known as: Loss or death of child | loss of child | death of child Excludes: Prolonged grief disorder [5C70.0] Dehydration Definition: Dehydration occurs when there is an insufficient amount or excessive loss of water in the body. This can be caused by vomiting, diarrhoea, fever, use of diuretics, profuse sweating, or decreased water intake. Also known as: Dehydration | fluid depletion | anhydration | anhydremia | fluid volume deficit [MB27.Z] Symptoms or signs of perceptual disturbance, unspecified Also known as: Symptoms or signs of perceptual disturbance, unspecified | Symptoms or signs involving perceptual disturbance | sensory loss [MG43.5] Excessive weight loss Definition: A reduction of total body mass, due to loss of fluid, body fat or adipose tissue, or lean (muscle) mass that is sufficient in quantity or rate to create risk to the individual’s health. Also known as: Excessive weight loss | abnormal decrease in weight | abnormal weight loss | unintended weight loss | weight loss NOS === GRAPH WALKS === --- Walk 1 --- [AB52] Deafness not otherwise specified --PARENT--> [?] Disorders with hearing impairment --PARENT--> [10] Diseases of the ear or mastoid process Def: This chapter contains diseases of the ear and diseases of the mastoid process.... --- Walk 2 --- [AB52] Deafness not otherwise specified --PARENT--> [?] Disorders with hearing impairment --EXCLUDES--> [?] Otosclerosis Def: Otosclerosis is a genetically mediated metabolic bone disease that affects the otic capsule and stapes. It is an autosomal dominant disorder with varying penetrance and expressivity. Usually symptomat... --- Walk 3 --- [QA00.7] Examination of ears and hearing --PARENT--> [QA00] General examination or investigation of persons without complaint or reported diagnosis --EXCLUDES--> [?] Special screening examination for infectious diseases Def: A reason for encounter to screen for an infection with a bacterial, viral, fungal, or parasitic source.... --- Walk 4 --- [QA00.7] Examination of ears and hearing --PARENT--> [QA00] General examination or investigation of persons without complaint or reported diagnosis --EXCLUDES--> [?] Special screening examination for infectious diseases Def: A reason for encounter to screen for an infection with a bacterial, viral, fungal, or parasitic source.... --- Walk 5 --- [MC4Y] Other specified symptoms or signs involving the ear or mastoid process --PARENT--> [?] Symptoms or signs involving the ear or mastoid process --CHILD--> [MC40] Plugged feeling ear --- Walk 6 --- [MC4Y] Other specified symptoms or signs involving the ear or mastoid process --PARENT--> [?] Symptoms or signs involving the ear or mastoid process --CHILD--> [MC4Y] Other specified symptoms or signs involving the ear or mastoid process
[ "[AB52] Deafness not otherwise specified\n --PARENT--> [?] Disorders with hearing impairment\n --PARENT--> [10] Diseases of the ear or mastoid process\n Def: This chapter contains diseases of the ear and diseases of the mastoid process....", "[AB52] Deafness not otherwise specified\n --PARENT--> [?] Disorders with hearing impairment\n --EXCLUDES--> [?] Otosclerosis\n Def: Otosclerosis is a genetically mediated metabolic bone disease that affects the otic capsule and stapes. It is an autosomal dominant disorder with varying penetrance and expressivity. Usually symptomat...", "[QA00.7] Examination of ears and hearing\n --PARENT--> [QA00] General examination or investigation of persons without complaint or reported diagnosis\n --EXCLUDES--> [?] Special screening examination for infectious diseases\n Def: A reason for encounter to screen for an infection with a bacterial, viral, fungal, or parasitic source....", "[QA00.7] Examination of ears and hearing\n --PARENT--> [QA00] General examination or investigation of persons without complaint or reported diagnosis\n --EXCLUDES--> [?] Special screening examination for infectious diseases\n Def: A reason for encounter to screen for an infection with a bacterial, viral, fungal, or parasitic source....", "[MC4Y] Other specified symptoms or signs involving the ear or mastoid process\n --PARENT--> [?] Symptoms or signs involving the ear or mastoid process\n --CHILD--> [MC40] Plugged feeling ear", "[MC4Y] Other specified symptoms or signs involving the ear or mastoid process\n --PARENT--> [?] Symptoms or signs involving the ear or mastoid process\n --CHILD--> [MC4Y] Other specified symptoms or signs involving the ear or mastoid process" ]
AB52
Deafness not otherwise specified
[ { "from_icd11": "AB52", "icd10_code": "H9190", "icd10_title": "Unspecified hearing loss, unspecified ear" }, { "from_icd11": "AB52", "icd10_code": "H9193", "icd10_title": "Unspecified hearing loss, bilateral" }, { "from_icd11": "QA00.7", "icd10_code": "Z011", "icd10_title": "Encounter for examination of ears and hearing" }, { "from_icd11": "AB54", "icd10_code": "H9113", "icd10_title": "Presbycusis, bilateral" }, { "from_icd11": "AB54", "icd10_code": "H9110", "icd10_title": "Presbycusis, unspecified ear" }, { "from_icd11": "AB54", "icd10_code": "H911", "icd10_title": "Presbycusis" }, { "from_icd11": "AB5Z", "icd10_code": "H9192", "icd10_title": "Unspecified hearing loss, left ear" }, { "from_icd11": "AB5Z", "icd10_code": "H9191", "icd10_title": "Unspecified hearing loss, right ear" }, { "from_icd11": "AB5Z", "icd10_code": "H9011", "icd10_title": "Conductive hearing loss, unilateral, right ear, with unrestricted hearing on the contralateral side" }, { "from_icd11": "AB5Z", "icd10_code": "H918X3", "icd10_title": "Other specified hearing loss, bilateral" }, { "from_icd11": "AB5Z", "icd10_code": "H918X9", "icd10_title": "Other specified hearing loss, unspecified ear" }, { "from_icd11": "AB5Z", "icd10_code": "H918X2", "icd10_title": "Other specified hearing loss, left ear" }, { "from_icd11": "AB5Z", "icd10_code": "H918X1", "icd10_title": "Other specified hearing loss, right ear" }, { "from_icd11": "AB5Z", "icd10_code": "H9012", "icd10_title": "Conductive hearing loss, unilateral, left ear, with unrestricted hearing on the contralateral side" }, { "from_icd11": "AB5Z", "icd10_code": "H913", "icd10_title": "Deaf nonspeaking, not elsewhere classified" } ]
H9190
Unspecified hearing loss, unspecified ear
A 32-year-old woman came for treatment of infertility in November 2005. She gave history of ectopic pregnancy on two occasions. First ectopic pregnancy occurred in left tube, which was treated with laparoscopic salpingectomy in the year 1999. Again she had ruptured ectopic pregnancy a year later in the same tube, which was managed by laparoscopic salpingectomy. She underwent hysterosalpingography, which showed block in the right fallopian tube. She had past history of abdominal Koch’s (tuberculosis), for which she had received anti-tubercular treatment for 9 months. She had one attempt of In Vitro Fertilization-Embryo Transfer (IVF-ET) in 2002, which had failed, and this was her second attempt. Three embryos were transferred; and 14 days later, the beta-hCG was 228 mIU/mL. A transvaginal scan at 6 weeks revealed one intrauterine gestational sac with fetal pole and fetal heart. There was also an extrauterine sac measuring 1.6 cm in right adnexal region with live fetus. This was confirmed by two different sonologists. The couple was explained about the severity of the situation, and the option to choose between laparoscopic salpingectomy and ultrasound-guided intra-cardiac instillations of potassium chloride (KCL) was offered. However the couple deferred for any form of treatment as she was a asymptomatic. We decided to keep her under observation by serial ultrasound scans and clinical examination.
3.707031
0.986816
sec[1]/p[0]
en
0.999996
21209757
https://doi.org/10.4103/0974-1208.69333
[ "which", "ectopic", "pregnancy", "tube", "laparoscopic", "salpingectomy", "attempt", "this", "fetal", "couple" ]
[ { "code": "BD50.41", "title": "Abdominal aortic aneurysm with rupture" }, { "code": "EK91", "title": "Dermatoses which may presage cutaneous lymphoma" }, { "code": "MH12.1", "title": "Death occurring less than 24 hours from onset of symptoms, not otherwise explained" }, { "code": "8A44.3", "title": "Certain specified leukodystrophies" }, { "code": "JA01.Z", "title": "Ectopic pregnancy, unspecified" }, { "code": "LB17.1", "title": "Ectopic anus" }, { "code": "LB30.7", "title": "Ectopic or pelvic kidney" }, { "code": "DA07.Y", "title": "Other specified disorders of tooth development or eruption" }, { "code": "BC9Y", "title": "Other specified cardiac arrhythmia" }, { "code": "JA80.Z", "title": "Maternal care related to unspecified multiple gestation" } ]
=== ICD-11 CODES FOUND === [BD50.41] Abdominal aortic aneurysm with rupture Also known as: Abdominal aortic aneurysm with rupture | abdominal aorta aneurysm rupture | abdominal aorta aneurysm ruptured | abdominal aortic aneurysm which has ruptured | ruptured AAA [EK91] Dermatoses which may presage cutaneous lymphoma Definition: Dermatoses which may represent the earliest stages of cutaneous lymphoma but where it is not possible to confirm their neoplastic nature. Also known as: Dermatoses which may presage cutaneous lymphoma [MH12.1] Death occurring less than 24 hours from onset of symptoms, not otherwise explained Also known as: Death occurring less than 24 hours from onset of symptoms, not otherwise explained | died without sign of disease | Death known not to be violent or instantaneous for which no cause can be discovered | death known not to be violent or instantaneous, cause unknown | Death without sign of disease Includes: Death known not to be violent or instantaneous for which no cause can be discovered | Death without sign of disease [8A44.3] Certain specified leukodystrophies Also known as: Certain specified leukodystrophies | CACH syndrome | Vanishing white matter disease | Childhood ataxia with central nervous system hypomyelination | Congenital or early infantile CACH syndrome [JA01.Z] Ectopic pregnancy, unspecified Also known as: Ectopic pregnancy, unspecified | Ectopic pregnancy | extrauterine gestation or pregnancy | extrauterine pregnancy | EP - [ectopic pregnancy] [LB17.1] Ectopic anus Definition: While children with imperforate or obviously mislocated anus are identified in the newborn period, some children with a very mild abnormality may escape identification until after the newborn period. This mild mislocation of the anus has been termed anterior ectopic anus. Anterior ectopic anus is different from imperforate anus with perineal fistula in that the anal opening is usually of normal size, and only mildly misplaced. Most of these children come to medical attention due to severe consti Also known as: Ectopic anus | Misplaced anus | Anal ectopia [LB30.7] Ectopic or pelvic kidney Definition: A birth defect characterised by an abnormally positioned kidney; may be asymptomatic or result in urine blockage, infection or kidney stones Also known as: Ectopic or pelvic kidney | Congenital displaced kidney | congenital misplaced kidney | congenital malposition of kidney | congenital prolapsed kidney Includes: Congenital displaced kidney | Malrotation of kidney [DA07.Y] Other specified disorders of tooth development or eruption Also known as: Other specified disorders of tooth development or eruption | Enamel hypoplasia | enamel hypoplasia of single tooth | hypoplasia of enamel of teeth | localised enamel or dentine hypoplasia [BC9Y] Other specified cardiac arrhythmia Also known as: Other specified cardiac arrhythmia | Ectopic arrhythmia | ectopic cardiac arrhythmia | ectopic atrial pacemaker | ectopic rhythm NOS [JA80.Z] Maternal care related to unspecified multiple gestation Also known as: Maternal care related to unspecified multiple gestation | Maternal care related to multiple gestation | multiple gestation, unspecified, unspecified trimester | multiple pregnancy | Multiple pregnancy NOS === GRAPH WALKS === --- Walk 1 --- [BD50.41] Abdominal aortic aneurysm with rupture --PARENT--> [BD50.4] Abdominal aortic aneurysm --PARENT--> [BD50] Aortic aneurysm or dissection Def: Aortic aneurysm is a term for any swelling (dilation or aneurysm) of the aorta to greater than 1.5 times normal, usually representing an underlying weakness in the wall of the aorta at that location. ... --- Walk 2 --- [BD50.41] Abdominal aortic aneurysm with rupture --PARENT--> [BD50.4] Abdominal aortic aneurysm --CHILD--> [BD50.4Z] Abdominal aortic aneurysm, without mention of perforation or rupture --- Walk 3 --- [EK91] Dermatoses which may presage cutaneous lymphoma Def: Dermatoses which may represent the earliest stages of cutaneous lymphoma but where it is not possible to confirm their neoplastic nature.... --CHILD--> [EK91.0] Large plaque parapsoriasis Def: Large plaque parapsoriasis is a chronic skin disorder characterised by the indolent development over years or decades of scaly patches or slightly elevated plaques which may be clinically indistinguis... --PARENT--> [EK91] Dermatoses which may presage cutaneous lymphoma Def: Dermatoses which may represent the earliest stages of cutaneous lymphoma but where it is not possible to confirm their neoplastic nature.... --- Walk 4 --- [EK91] Dermatoses which may presage cutaneous lymphoma Def: Dermatoses which may represent the earliest stages of cutaneous lymphoma but where it is not possible to confirm their neoplastic nature.... --PARENT--> [?] Disorders of the skin of uncertain or unpredictable malignant potential --PARENT--> [14] Diseases of the skin Def: Diseases of the skin incorporate conditions affecting the epidermis, its appendages (hair, hair follicle, sebaceous glands, apocrine sweat gland apparatus, eccrine sweat gland apparatus and nails) and... --- Walk 5 --- [MH12.1] Death occurring less than 24 hours from onset of symptoms, not otherwise explained --PARENT--> [MH12] Other sudden death, cause unknown --CHILD--> [MH12.1] Death occurring less than 24 hours from onset of symptoms, not otherwise explained --- Walk 6 --- [MH12.1] Death occurring less than 24 hours from onset of symptoms, not otherwise explained --PARENT--> [MH12] Other sudden death, cause unknown --CHILD--> [MH12.0] Instantaneous death
[ "[BD50.41] Abdominal aortic aneurysm with rupture\n --PARENT--> [BD50.4] Abdominal aortic aneurysm\n --PARENT--> [BD50] Aortic aneurysm or dissection\n Def: Aortic aneurysm is a term for any swelling (dilation or aneurysm) of the aorta to greater than 1.5 times normal, usually representing an underlying weakness in the wall of the aorta at that location. ...", "[BD50.41] Abdominal aortic aneurysm with rupture\n --PARENT--> [BD50.4] Abdominal aortic aneurysm\n --CHILD--> [BD50.4Z] Abdominal aortic aneurysm, without mention of perforation or rupture", "[EK91] Dermatoses which may presage cutaneous lymphoma\n Def: Dermatoses which may represent the earliest stages of cutaneous lymphoma but where it is not possible to confirm their neoplastic nature....\n --CHILD--> [EK91.0] Large plaque parapsoriasis\n Def: Large plaque parapsoriasis is a chronic skin disorder characterised by the indolent development over years or decades of scaly patches or slightly elevated plaques which may be clinically indistinguis...\n --PARENT--> [EK91] Dermatoses which may presage cutaneous lymphoma\n Def: Dermatoses which may represent the earliest stages of cutaneous lymphoma but where it is not possible to confirm their neoplastic nature....", "[EK91] Dermatoses which may presage cutaneous lymphoma\n Def: Dermatoses which may represent the earliest stages of cutaneous lymphoma but where it is not possible to confirm their neoplastic nature....\n --PARENT--> [?] Disorders of the skin of uncertain or unpredictable malignant potential\n --PARENT--> [14] Diseases of the skin\n Def: Diseases of the skin incorporate conditions affecting the epidermis, its appendages (hair, hair follicle, sebaceous glands, apocrine sweat gland apparatus, eccrine sweat gland apparatus and nails) and...", "[MH12.1] Death occurring less than 24 hours from onset of symptoms, not otherwise explained\n --PARENT--> [MH12] Other sudden death, cause unknown\n --CHILD--> [MH12.1] Death occurring less than 24 hours from onset of symptoms, not otherwise explained", "[MH12.1] Death occurring less than 24 hours from onset of symptoms, not otherwise explained\n --PARENT--> [MH12] Other sudden death, cause unknown\n --CHILD--> [MH12.0] Instantaneous death" ]
BD50.41
Abdominal aortic aneurysm with rupture
[ { "from_icd11": "BD50.41", "icd10_code": "I713", "icd10_title": "Abdominal aortic aneurysm, ruptured" }, { "from_icd11": "EK91", "icd10_code": "L989", "icd10_title": "Disorder of the skin and subcutaneous tissue, unspecified" }, { "from_icd11": "MH12.1", "icd10_code": "R961", "icd10_title": "" }, { "from_icd11": "JA01.Z", "icd10_code": "O0081", "icd10_title": "Other ectopic pregnancy with intrauterine pregnancy" }, { "from_icd11": "JA01.Z", "icd10_code": "O0080", "icd10_title": "Other ectopic pregnancy without intrauterine pregnancy" }, { "from_icd11": "JA01.Z", "icd10_code": "O0090", "icd10_title": "Unspecified ectopic pregnancy without intrauterine pregnancy" }, { "from_icd11": "JA01.Z", "icd10_code": "O008", "icd10_title": "Other ectopic pregnancy" }, { "from_icd11": "JA01.Z", "icd10_code": "O009", "icd10_title": "Ectopic pregnancy, unspecified" }, { "from_icd11": "JA01.Z", "icd10_code": "O00", "icd10_title": "Ectopic pregnancy" }, { "from_icd11": "LB17.1", "icd10_code": "Q435", "icd10_title": "Ectopic anus" }, { "from_icd11": "LB30.7", "icd10_code": "Q632", "icd10_title": "Ectopic kidney" }, { "from_icd11": "LB30.7", "icd10_code": "Q63", "icd10_title": "Other congenital malformations of kidney" }, { "from_icd11": "JA80.Z", "icd10_code": "O30", "icd10_title": "Multiple gestation" }, { "from_icd11": "JA80.Z", "icd10_code": "O308", "icd10_title": "Other specified multiple gestation" }, { "from_icd11": "JA80.Z", "icd10_code": "O309", "icd10_title": "Multiple gestation, unspecified" } ]
I713
Abdominal aortic aneurysm, ruptured
Odontoid fractures have been reported in the literature to be commonest in Type II variety 11 as also in our series (11 of 13). Undisplaced fractures without significant mobility on flexion/extension X-rays are treated conservatively, usually with a halo vest immobilization [ Figure 3 ]. Displaced, non-comminuted, fresh and reducible Type II fractures were treated with anterior odontoid screw fixation [ Figure 4 ]. We put in a single odontoid screw and found putting in two screws was technically not feasible. The biomechanical 12 and clinical 13 studies in literature give ample efficacy of the same. Comminuted, non-reducible and/or late presentation of Type II fractures was treated with posterior instrumented C1-C2 fusion. In two of them we had to resort to wiring technique because the lack of reduction negates an attempt of transarticular screw fixation. In both these, we had to immobilize them postoperatively with SOMI brace for three months. Those who underwent transarticular screw fixation had a very stable construct and did not require postoperative immobilization as suggested by Magerl. 14 We did not have any serious technique related complications and the contemporary publications also vouch for their safety. Reported incidence of fusion is about 98% 15 and the incidence of vertebral artery injury is about 2.2% per screw with the incidence of neurological complications being about 0.1%. 16
3.992188
0.51416
sec[2]/p[4]
en
0.999995
21139783
https://doi.org/10.4103/0019-5413.36992
[ "screw", "fractures", "odontoid", "type", "treated", "fixation", "incidence", "about", "literature", "immobilization" ]
[ { "code": "QB84", "title": "Follow-up care involving removal of fracture plate or other internal fixation device" }, { "code": "DA21.20", "title": "Hypertensive peristalsis" }, { "code": "PK99.3", "title": "Orthopaedic devices associated with injury or harm, surgical instruments, materials or devices" }, { "code": "ND56.2", "title": "Fracture of unspecified body region" }, { "code": "ND32", "title": "Fractures involving multiple body regions" }, { "code": "NB52.Z", "title": "Fracture of lumbar spine or pelvis, unspecified" }, { "code": "FB80.B", "title": "Pathological fracture" }, { "code": "FB80.Y", "title": "Other specified disorders of bone density or structure" }, { "code": "NA22.12", "title": "Fracture of odontoid process" }, { "code": "LB73.23", "title": "Aplasia or hypoplasia of the odontoid process of axis" } ]
=== ICD-11 CODES FOUND === [QB84] Follow-up care involving removal of fracture plate or other internal fixation device Also known as: Follow-up care involving removal of fracture plate or other internal fixation device | Change of internal fixation device | change of fixation device | change of Kirschner wire | Checking of internal fixation device Excludes: removal of external fixation device [DA21.20] Hypertensive peristalsis Definition: This is a motility disorder of oesophagus characterised by hypertensive peristalsis. This motility abnormality includes nutcracker oesophagus that has been reported in association with dysphagia, non-cardiac chest pain, and heartburn. Also known as: Hypertensive peristalsis | Bársony-Polgár Syndrome II | corkscrew oesophagus | curling of oesophagus | Nutcracker oesophagus [PK99.3] Orthopaedic devices associated with injury or harm, surgical instruments, materials or devices Definition: Orthopaedic related surgical instruments like materials and devices (including sutures) were involved in an adverse related incident Also known as: Orthopaedic devices associated with injury or harm, surgical instruments, materials or devices | Orthopaedic devices associated with injury or harm, suture material | Orthopaedic devices associated with injury or harm, scalpel | Orthopaedic devices associated with injury or harm, cautery device | Orthopaedic devices associated with injury or harm, laser Excludes: Circumstances associated with a surgical or other medical device influencing the episode of care without injury or harm [ND56.2] Fracture of unspecified body region Also known as: Fracture of unspecified body region | avulsion fracture of unspecified body site | comminuted fracture of unspecified body site | compression fracture of unspecified body site | fracture dislocation of unspecified body site Excludes: multiple fractures NOS [ND32] Fractures involving multiple body regions Also known as: Fractures involving multiple body regions | multiple skeletal fractures | multiple fractures | multiple compression fractures | fracture of multiple bone sites [NB52.Z] Fracture of lumbar spine or pelvis, unspecified Also known as: Fracture of lumbar spine or pelvis, unspecified | Fracture of lumbar spine or pelvis | Fracture of pelvis, not elsewhere classified | fracture pelvis NOS | pelvic fracture [FB80.B] Pathological fracture Also known as: Pathological fracture | pathological bone fracture | Pathological fracture NOS | spontaneous fracture | spontaneous fracture with dislocation Excludes: Collapsed vertebra, not elsewhere classified [FB80.Y] Other specified disorders of bone density or structure Also known as: Other specified disorders of bone density or structure | Bone dysplasia | Inherited bone dysplasia | Acquired bone dysplasia | Drug-induced bone dysplasia [NA22.12] Fracture of odontoid process Also known as: Fracture of odontoid process | Fracture of dens | Fracture of dens, Type I | Fracture of dens, Type II | Fracture of dens, Type III [LB73.23] Aplasia or hypoplasia of the odontoid process of axis Also known as: Aplasia or hypoplasia of the odontoid process of axis === GRAPH WALKS === --- Walk 1 --- [QB84] Follow-up care involving removal of fracture plate or other internal fixation device --EXCLUDES--> [?] Follow-up care involving removal of external fixation device --PARENT--> [?] Contact with health services for specific surgical interventions --- Walk 2 --- [QB84] Follow-up care involving removal of fracture plate or other internal fixation device --EXCLUDES--> [?] Follow-up care involving removal of external fixation device --PARENT--> [?] Contact with health services for specific surgical interventions --- Walk 3 --- [DA21.20] Hypertensive peristalsis Def: This is a motility disorder of oesophagus characterised by hypertensive peristalsis. This motility abnormality includes nutcracker oesophagus that has been reported in association with dysphagia, non-... --PARENT--> [DA21.2] Disorder of oesophageal peristalsis Def: Disorder of oesophageal peristalsis is part of a spectrum of motility disorders in the thoracic oesophagus characterised by dysphagia and chest pain due to incoordination of oesophageal peristaltic co... --CHILD--> [DA21.20] Hypertensive peristalsis Def: This is a motility disorder of oesophagus characterised by hypertensive peristalsis. This motility abnormality includes nutcracker oesophagus that has been reported in association with dysphagia, non-... --- Walk 4 --- [DA21.20] Hypertensive peristalsis Def: This is a motility disorder of oesophagus characterised by hypertensive peristalsis. This motility abnormality includes nutcracker oesophagus that has been reported in association with dysphagia, non-... --PARENT--> [DA21.2] Disorder of oesophageal peristalsis Def: Disorder of oesophageal peristalsis is part of a spectrum of motility disorders in the thoracic oesophagus characterised by dysphagia and chest pain due to incoordination of oesophageal peristaltic co... --PARENT--> [DA21] Motility disorders of oesophagus Def: This group incorporates oesophageal disorders due to disturbances of oesophageal motor function.... --- Walk 5 --- [PK99.3] Orthopaedic devices associated with injury or harm, surgical instruments, materials or devices Def: Orthopaedic related surgical instruments like materials and devices (including sutures) were involved in an adverse related incident... --PARENT--> [PK99] Orthopaedic devices, implants or grafts associated with injury or harm --CHILD--> [PK99.0] Orthopaedic devices associated with injury or harm, diagnostic or monitoring devices Def: An orthopaedic device was involved in an incident that occurred in a diagnostic or monitoring task... --- Walk 6 --- [PK99.3] Orthopaedic devices associated with injury or harm, surgical instruments, materials or devices Def: Orthopaedic related surgical instruments like materials and devices (including sutures) were involved in an adverse related incident... --EXCLUDES--> [?] Circumstances associated with a surgical or other medical device influencing the episode of care without injury or harm --CHILD--> [?] Dislodgement, misconnection or de-attachment of a surgical or medical device without injury or harm Def: A device that has moved out of place, become disconnected, loosened or unstable, but without documented injury or harm....
[ "[QB84] Follow-up care involving removal of fracture plate or other internal fixation device\n --EXCLUDES--> [?] Follow-up care involving removal of external fixation device\n --PARENT--> [?] Contact with health services for specific surgical interventions", "[QB84] Follow-up care involving removal of fracture plate or other internal fixation device\n --EXCLUDES--> [?] Follow-up care involving removal of external fixation device\n --PARENT--> [?] Contact with health services for specific surgical interventions", "[DA21.20] Hypertensive peristalsis\n Def: This is a motility disorder of oesophagus characterised by hypertensive peristalsis. This motility abnormality includes nutcracker oesophagus that has been reported in association with dysphagia, non-...\n --PARENT--> [DA21.2] Disorder of oesophageal peristalsis\n Def: Disorder of oesophageal peristalsis is part of a spectrum of motility disorders in the thoracic oesophagus characterised by dysphagia and chest pain due to incoordination of oesophageal peristaltic co...\n --CHILD--> [DA21.20] Hypertensive peristalsis\n Def: This is a motility disorder of oesophagus characterised by hypertensive peristalsis. This motility abnormality includes nutcracker oesophagus that has been reported in association with dysphagia, non-...", "[DA21.20] Hypertensive peristalsis\n Def: This is a motility disorder of oesophagus characterised by hypertensive peristalsis. This motility abnormality includes nutcracker oesophagus that has been reported in association with dysphagia, non-...\n --PARENT--> [DA21.2] Disorder of oesophageal peristalsis\n Def: Disorder of oesophageal peristalsis is part of a spectrum of motility disorders in the thoracic oesophagus characterised by dysphagia and chest pain due to incoordination of oesophageal peristaltic co...\n --PARENT--> [DA21] Motility disorders of oesophagus\n Def: This group incorporates oesophageal disorders due to disturbances of oesophageal motor function....", "[PK99.3] Orthopaedic devices associated with injury or harm, surgical instruments, materials or devices\n Def: Orthopaedic related surgical instruments like materials and devices (including sutures) were involved in an adverse related incident...\n --PARENT--> [PK99] Orthopaedic devices, implants or grafts associated with injury or harm\n --CHILD--> [PK99.0] Orthopaedic devices associated with injury or harm, diagnostic or monitoring devices\n Def: An orthopaedic device was involved in an incident that occurred in a diagnostic or monitoring task...", "[PK99.3] Orthopaedic devices associated with injury or harm, surgical instruments, materials or devices\n Def: Orthopaedic related surgical instruments like materials and devices (including sutures) were involved in an adverse related incident...\n --EXCLUDES--> [?] Circumstances associated with a surgical or other medical device influencing the episode of care without injury or harm\n --CHILD--> [?] Dislodgement, misconnection or de-attachment of a surgical or medical device without injury or harm\n Def: A device that has moved out of place, become disconnected, loosened or unstable, but without documented injury or harm...." ]
QB84
Follow-up care involving removal of fracture plate or other internal fixation device
[ { "from_icd11": "QB84", "icd10_code": "Z4733", "icd10_title": "Aftercare following explantation of knee joint prosthesis" }, { "from_icd11": "QB84", "icd10_code": "Z4732", "icd10_title": "Aftercare following explantation of hip joint prosthesis" }, { "from_icd11": "QB84", "icd10_code": "Z472", "icd10_title": "Encounter for removal of internal fixation device" }, { "from_icd11": "QB84", "icd10_code": "Z471", "icd10_title": "Aftercare following joint replacement surgery" }, { "from_icd11": "QB84", "icd10_code": "Z4731", "icd10_title": "Aftercare following explantation of shoulder joint prosthesis" }, { "from_icd11": "QB84", "icd10_code": "Z4781", "icd10_title": "Encounter for orthopedic aftercare following surgical amputation" }, { "from_icd11": "QB84", "icd10_code": "Z4789", "icd10_title": "Encounter for other orthopedic aftercare" }, { "from_icd11": "QB84", "icd10_code": "Z47", "icd10_title": "Orthopedic aftercare" }, { "from_icd11": "QB84", "icd10_code": "Z470", "icd10_title": "" }, { "from_icd11": "QB84", "icd10_code": "Z478", "icd10_title": "Encounter for other orthopedic aftercare" }, { "from_icd11": "QB84", "icd10_code": "Z479", "icd10_title": "" }, { "from_icd11": "DA21.20", "icd10_code": "K224", "icd10_title": "Dyskinesia of esophagus" }, { "from_icd11": "PK99.3", "icd10_code": "T84114A", "icd10_title": "Breakdown (mechanical) of internal fixation device of right femur, initial encounter" }, { "from_icd11": "PK99.3", "icd10_code": "T84125A", "icd10_title": "Displacement of internal fixation device of left femur, initial encounter" }, { "from_icd11": "PK99.3", "icd10_code": "T84197A", "icd10_title": "Other mechanical complication of internal fixation device of bone of left lower leg, initial encounter" } ]
Z4733
Aftercare following explantation of knee joint prosthesis
A tracheostomy tube (Yunshin Medical Co., Bucheon, Korea) and an esophageal feeding tube (Sewoon Medical Co., Cheonan, Korea) were placed to alleviate the clinical signs of dyspnea and to assist enteral feeding, respectively. A constant-rate infusion of cefotaxime (Kukje Pharm, Sungnam, Korea) was initiated at 2 mg/kg/h following a loading dose of 20 mg/kg. Butorphanol was administered intravenously at a dose of 0.2 mg/kg every 6 h. Oral prednisolone was also initiated at 0.25 mg/kg twice a day to improve surgery-induced neuroinflammation. Oropharyngeal secretions and tracheal sputum were aspirated through a tracheostomy tube every 6 h. A soft canned diet (Recovery, Royal Canin Veterinary Diet, MO, USA) was given four times a day for 15 min through the esophageal feeding tube. The oral cavity was then rinsed twice daily with 0.12% chlorhexidine gluconate (Hexamedin; Bukwang Pharm., Seoul, Korea). On the 6th postoperative day, the patient achieved full weight bearing and became mobile without any signs of pain. On the repeated radiographs on the same day, the patient was shown to have recovered from aspiratory pneumonia. However, the multiple CN palsies did not show any significant improvement, and the tongue gradually protruded to the right lateral side . The multiple CN palsies thought to involve the 9th, 10th, and 12th CNs did not improve and slowly deteriorated even at 2 weeks postoperatively.
3.832031
0.968262
sec[1]/p[4]
en
0.999998
35878339
https://doi.org/10.3390/vetsci9070322
[ "tube", "korea", "feeding", "tracheostomy", "esophageal", "pharm", "initiated", "every", "oral", "twice" ]
[ { "code": "GA07.Z&XA3EF0", "title": "Inflammatory disease of fallopian tube" }, { "code": "JA01.1", "title": "Tubal pregnancy" }, { "code": "GB90.Y", "title": "Other specified disorders of kidney or ureter" }, { "code": "GB54", "title": "Tubulo-interstitial nephritis, not specified as acute or chronic" }, { "code": "AB10.Z", "title": "Disorders of Eustachian tube, unspecified" }, { "code": "MG43.3Z", "title": "Feeding difficulties, unspecified" }, { "code": "MG43.32", "title": "Feeding problem of adult" }, { "code": "MG43.31", "title": "Feeding problem of child" }, { "code": "6B8Z", "title": "Feeding or eating disorders, unspecified" }, { "code": "MG43.30", "title": "Feeding problem of infant" } ]
=== ICD-11 CODES FOUND === [JA01.1] Tubal pregnancy Definition: A condition characterised by implantation of the embryo within the fallopian tube (ampullary, isthmus, interstitium) during pregnancy. Also known as: Tubal pregnancy | Fallopian pregnancy | fallopian tube pregnancy | Tubal abortion | Rupture of fallopian tube due to pregnancy Includes: Fallopian pregnancy | Tubal abortion [GB90.Y] Other specified disorders of kidney or ureter Also known as: Other specified disorders of kidney or ureter | Other secondary disorders of kidney or ureter | Other disorders of kidney and ureter NEC | Inflammatory diseases of the renal pelvis or the ureter without tubulo-interstitial nephritis | Infectious diseases of the renal pelvis or the ureter without tubulo-interstitial nephritis [GB54] Tubulo-interstitial nephritis, not specified as acute or chronic Definition: A disease characterised by inflammation of and damage to tubules or the interstitium of the kidney while sparing the glomeruli secondary to immune reaction or toxic agent. Also known as: Tubulo-interstitial nephritis, not specified as acute or chronic | tubulo-interstitial nephritis | renal disease with interstitial nephritis | Congenital pyelitis | Cystopyelitis Excludes: calculous pyelonephritis [AB10.Z] Disorders of Eustachian tube, unspecified Also known as: Disorders of Eustachian tube, unspecified | Disorders of Eustachian tube | auditory tube disorder | disease of Eustachian tube | Eustachian tube dysfunction [MG43.3Z] Feeding difficulties, unspecified Also known as: Feeding difficulties, unspecified | Feeding difficulties | difficult feeding | faulty feeding | Feeding difficulties and mismanagement [MG43.32] Feeding problem of adult Also known as: Feeding problem of adult Excludes: Anorexia Nervosa | Bulimia Nervosa | Binge eating disorder [MG43.31] Feeding problem of child Also known as: Feeding problem of child Excludes: Feeding or eating disorders | Anorexia Nervosa | Avoidant-restrictive food intake disorder [6B8Z] Feeding or eating disorders, unspecified Also known as: Feeding or eating disorders, unspecified | Eating disorder, not elsewhere classified | eating disorder NOS [MG43.30] Feeding problem of infant Also known as: Feeding problem of infant Excludes: Feeding problems of newborn | Avoidant-restrictive food intake disorder === GRAPH WALKS === --- Walk 1 --- [JA01.1] Tubal pregnancy Def: A condition characterised by implantation of the embryo within the fallopian tube (ampullary, isthmus, interstitium) during pregnancy.... --PARENT--> [JA01] Ectopic pregnancy Def: Any condition characterised by implantation of the embryo outside the endometrium and endometrial cavity during pregnancy.... --CHILD--> [JA01.2] Ovarian pregnancy Def: A condition characterised by implantation of the embryo within the ovary during pregnancy.... --- Walk 2 --- [JA01.1] Tubal pregnancy Def: A condition characterised by implantation of the embryo within the fallopian tube (ampullary, isthmus, interstitium) during pregnancy.... --PARENT--> [JA01] Ectopic pregnancy Def: Any condition characterised by implantation of the embryo outside the endometrium and endometrial cavity during pregnancy.... --CHILD--> [JA01.2] Ovarian pregnancy Def: A condition characterised by implantation of the embryo within the ovary during pregnancy.... --- Walk 3 --- [GB90.Y] Other specified disorders of kidney or ureter --PARENT--> [GB90] Certain specified disorders of kidney or ureter Def: Any disorder characterised by pathological changes to the kidney or ureter.... --CHILD--> [GB90.0] Nephroptosis Def: Enhanced mobility of the kidney, resulting in ptosis when the patient is upright. More common on the right, associated with a longer renal artery, and debatably associated with fibromuscular hyperplas... --- Walk 4 --- [GB90.Y] Other specified disorders of kidney or ureter --PARENT--> [GB90] Certain specified disorders of kidney or ureter Def: Any disorder characterised by pathological changes to the kidney or ureter.... --RELATED_TO--> [?] Postinterventional ischemia or infarction of kidney Def: This refers to a restriction in blood supply to tissues of the kidney due to a health care intervention causing a shortage of oxygen and glucose needed for cellular metabolism resulting in the death o... --- Walk 5 --- [GB54] Tubulo-interstitial nephritis, not specified as acute or chronic Def: A disease characterised by inflammation of and damage to tubules or the interstitium of the kidney while sparing the glomeruli secondary to immune reaction or toxic agent.... --EXCLUDES--> [?] Calculus of upper urinary tract Def: A condition of the urinary system, caused by dehydration, decreased urine volume or fluid flow rates, or increased excretion of minerals such as calcium, oxalate, magnesium, cystine, and phosphate. Th... --PARENT--> [?] Urolithiasis Def: A condition of the urinary system, caused by dehydration, decreased urine volume or fluid flow rates, or increased excretion of minerals such as calcium, oxalate, magnesium, cystine, and phosphate. Th... --- Walk 6 --- [GB54] Tubulo-interstitial nephritis, not specified as acute or chronic Def: A disease characterised by inflammation of and damage to tubules or the interstitium of the kidney while sparing the glomeruli secondary to immune reaction or toxic agent.... --PARENT--> [?] Renal tubulo-interstitial diseases Def: Any disease characterised by pathological changes to the renal tubules and interstitial tissues.... --CHILD--> [GB52] Acute tubular necrosis Def: Any condition of the kidney, caused by hypotension, hypoperfusion, ischaemia, hypoxia, or use of nephrotoxic drugs. These conditions are characterised by death of tubular epithelial cells and acute ki...
[ "[JA01.1] Tubal pregnancy\n Def: A condition characterised by implantation of the embryo within the fallopian tube (ampullary, isthmus, interstitium) during pregnancy....\n --PARENT--> [JA01] Ectopic pregnancy\n Def: Any condition characterised by implantation of the embryo outside the endometrium and endometrial cavity during pregnancy....\n --CHILD--> [JA01.2] Ovarian pregnancy\n Def: A condition characterised by implantation of the embryo within the ovary during pregnancy....", "[JA01.1] Tubal pregnancy\n Def: A condition characterised by implantation of the embryo within the fallopian tube (ampullary, isthmus, interstitium) during pregnancy....\n --PARENT--> [JA01] Ectopic pregnancy\n Def: Any condition characterised by implantation of the embryo outside the endometrium and endometrial cavity during pregnancy....\n --CHILD--> [JA01.2] Ovarian pregnancy\n Def: A condition characterised by implantation of the embryo within the ovary during pregnancy....", "[GB90.Y] Other specified disorders of kidney or ureter\n --PARENT--> [GB90] Certain specified disorders of kidney or ureter\n Def: Any disorder characterised by pathological changes to the kidney or ureter....\n --CHILD--> [GB90.0] Nephroptosis\n Def: Enhanced mobility of the kidney, resulting in ptosis when the patient is upright. More common on the right, associated with a longer renal artery, and debatably associated with fibromuscular hyperplas...", "[GB90.Y] Other specified disorders of kidney or ureter\n --PARENT--> [GB90] Certain specified disorders of kidney or ureter\n Def: Any disorder characterised by pathological changes to the kidney or ureter....\n --RELATED_TO--> [?] Postinterventional ischemia or infarction of kidney\n Def: This refers to a restriction in blood supply to tissues of the kidney due to a health care intervention causing a shortage of oxygen and glucose needed for cellular metabolism resulting in the death o...", "[GB54] Tubulo-interstitial nephritis, not specified as acute or chronic\n Def: A disease characterised by inflammation of and damage to tubules or the interstitium of the kidney while sparing the glomeruli secondary to immune reaction or toxic agent....\n --EXCLUDES--> [?] Calculus of upper urinary tract\n Def: A condition of the urinary system, caused by dehydration, decreased urine volume or fluid flow rates, or increased excretion of minerals such as calcium, oxalate, magnesium, cystine, and phosphate. Th...\n --PARENT--> [?] Urolithiasis\n Def: A condition of the urinary system, caused by dehydration, decreased urine volume or fluid flow rates, or increased excretion of minerals such as calcium, oxalate, magnesium, cystine, and phosphate. Th...", "[GB54] Tubulo-interstitial nephritis, not specified as acute or chronic\n Def: A disease characterised by inflammation of and damage to tubules or the interstitium of the kidney while sparing the glomeruli secondary to immune reaction or toxic agent....\n --PARENT--> [?] Renal tubulo-interstitial diseases\n Def: Any disease characterised by pathological changes to the renal tubules and interstitial tissues....\n --CHILD--> [GB52] Acute tubular necrosis\n Def: Any condition of the kidney, caused by hypotension, hypoperfusion, ischaemia, hypoxia, or use of nephrotoxic drugs. These conditions are characterised by death of tubular epithelial cells and acute ki..." ]
GA07.Z&XA3EF0
Inflammatory disease of fallopian tube
[ { "from_icd11": "JA01.1", "icd10_code": "O00102", "icd10_title": "Left tubal pregnancy without intrauterine pregnancy" }, { "from_icd11": "JA01.1", "icd10_code": "O0010", "icd10_title": "Tubal pregnancy without intrauterine pregnancy" }, { "from_icd11": "JA01.1", "icd10_code": "O00101", "icd10_title": "Right tubal pregnancy without intrauterine pregnancy" }, { "from_icd11": "JA01.1", "icd10_code": "O00111", "icd10_title": "Right tubal pregnancy with intrauterine pregnancy" }, { "from_icd11": "JA01.1", "icd10_code": "O001", "icd10_title": "Tubal pregnancy" }, { "from_icd11": "GB54", "icd10_code": "N12", "icd10_title": "Tubulo-interstitial nephritis, not specified as acute or chronic" }, { "from_icd11": "AB10.Z", "icd10_code": "H6991", "icd10_title": "Unspecified Eustachian tube disorder, right ear" }, { "from_icd11": "AB10.Z", "icd10_code": "H6981", "icd10_title": "Other specified disorders of Eustachian tube, right ear" }, { "from_icd11": "AB10.Z", "icd10_code": "H6980", "icd10_title": "Other specified disorders of Eustachian tube, unspecified ear" }, { "from_icd11": "AB10.Z", "icd10_code": "H6982", "icd10_title": "Other specified disorders of Eustachian tube, left ear" }, { "from_icd11": "AB10.Z", "icd10_code": "H6990", "icd10_title": "Unspecified Eustachian tube disorder, unspecified ear" }, { "from_icd11": "AB10.Z", "icd10_code": "H68", "icd10_title": "Eustachian salpingitis and obstruction" }, { "from_icd11": "AB10.Z", "icd10_code": "H69", "icd10_title": "Other and unspecified disorders of Eustachian tube" }, { "from_icd11": "AB10.Z", "icd10_code": "H698", "icd10_title": "Other specified disorders of Eustachian tube" }, { "from_icd11": "AB10.Z", "icd10_code": "H699", "icd10_title": "Unspecified Eustachian tube disorder" } ]
O00102
Left tubal pregnancy without intrauterine pregnancy
Complications such as coronary artery occlusion have been reported in cases of RF energy delivery through the aortic sinus of Valsalva . To avoid complications associated with RF ablation in coronary cusps, it is advocated that the distance between the ablation catheter tip and the ostium of the left and right coronary artery should be more than 1.0 cm before RF energy is applied, and the tip temperature should be maintained below 55 Cº to avoid perforating the sinus of Valsalva, which would damage the aortic valve and cause coronary occlusion . We noticed RBBB following ablation of the AP. However on reviewing the recordings it was noted that he had similar morphology and QRS axis in the beats where the AP was refractory prior to ablation. Therefore it could be concluded that it was not a complication related to the ablation in the NCC. The first degree AV block seen on follow up could be related to multiple causes like multiple ablations in the antero-septum in the first and second EP study, ablation in the NCC or hypervagotonia. His PR interval after ablation was noted to be 165 ms however on follow up was detected to have first degree AV block possibly implying effect of vagal tone or delayed effect of ablation. His PR interval shortened to 120 ms with a heart rate >150 beats per minute during the exercise stress test. This favors effect of vagal tone as the etiology of prolonged PR interval.
4.164063
0.54834
sec[2]/p[3]
en
0.999997
22665961
N/A
[ "ablation", "coronary", "that", "interval", "effect", "complications", "artery", "occlusion", "energy", "aortic" ]
[ { "code": "QF01.10", "title": "Acquired absence of female genital organs" }, { "code": "9B73.3", "title": "Serous retinal detachment" }, { "code": "JA8C.Z", "title": "Maternal care related to premature separation of placenta, unspecified" }, { "code": "KA02.Y", "title": "Fetus or newborn affected by other specified complication of placenta" }, { "code": "5D40.00", "title": "Hypothyroidism postradioactive iodine ablation" }, { "code": "BA8Z", "title": "Diseases of coronary artery, unspecified" }, { "code": "BA4Z", "title": "Acute ischaemic heart disease, unspecified" }, { "code": "BA41.Z", "title": "Acute myocardial infarction, unspecified" }, { "code": "BA5Z", "title": "Chronic ischaemic heart disease, unspecified" }, { "code": "LA8C.2", "title": "Congenital coronary arterial fistula" } ]
=== ICD-11 CODES FOUND === [QF01.10] Acquired absence of female genital organs Also known as: Acquired absence of female genital organs | Acquired absence of cervix | amputation of cervix | Acquired absence of the uterus | acquired uterine absence [9B73.3] Serous retinal detachment Definition: This occurs due to inflammation, injury or vascular abnormalities that results in fluid accumulating underneath the retina without the presence of a hole, tear, or break. Also known as: Serous retinal detachment | serous retinal detachment, unspecified eye | sensory retinal detachment | Retinal detachment without retinal break | Retinal detachment NOS Excludes: Central serous chorioretinopathy [JA8C.Z] Maternal care related to premature separation of placenta, unspecified Also known as: Maternal care related to premature separation of placenta, unspecified | Maternal care related to premature separation of placenta | ablatio placentae | detachment of placenta | placenta abruptio [KA02.Y] Fetus or newborn affected by other specified complication of placenta Also known as: Fetus or newborn affected by other specified complication of placenta | Fetus or newborn affected by other forms of placental separation | Ablatio placentae affecting fetus or newborn | placenta ablation affecting fetus or newborn | Abruptio placentae affecting fetus or newborn [5D40.00] Hypothyroidism postradioactive iodine ablation Also known as: Hypothyroidism postradioactive iodine ablation [BA8Z] Diseases of coronary artery, unspecified Also known as: Diseases of coronary artery, unspecified | coronary artery insufficiency | coronary artery heart disease | CAD - [coronary artery disease] | coronary artery disorder [BA4Z] Acute ischaemic heart disease, unspecified Also known as: Acute ischaemic heart disease, unspecified | acute coronary syndrome | ACS - [acute coronary syndrome] | Silent myocardial ischaemia | asymptomatic ischemia [BA41.Z] Acute myocardial infarction, unspecified Also known as: Acute myocardial infarction, unspecified | Acute myocardial infarction | cardiac attack | heart attack | acute cardiac infarction [BA5Z] Chronic ischaemic heart disease, unspecified Also known as: Chronic ischaemic heart disease, unspecified | Ischaemic heart disease (chronic) NOS | coronary ischaemia | coronary damage NOS | atheroma of heart [LA8C.2] Congenital coronary arterial fistula Definition: A congenital cardiovascular malformation in which a coronary artery communicates, through an anomalous channel, with a cardiac chamber or with any segment of the systemic or pulmonary circulation. Additional information: this communication may be simple and direct or may be tortuous and dilated. In order of frequency the involved coronary artery is the right, the left and, rarely, both coronary arteries. Occasionally multiple fistulas are present. Also known as: Congenital coronary arterial fistula | coronary fistula | congenital arteriovenous coronary fistula | congenital coronary fistula to pulmonary artery | Congenital coronary arterial fistula to right ventricle Includes: congenital coronary fistula to pulmonary artery Excludes: anomalous origin of coronary artery from pulmonary arterial tree === GRAPH WALKS === --- Walk 1 --- [QF01.10] Acquired absence of female genital organs --RELATED_TO--> [?] Traumatic amputation of entire vulva --EXCLUDES--> [?] Female Genital Mutilation Def: A condition caused by procedures or other interventions for non-medical purposes. This condition is characterised by the partial or total removal of the external female genitalia or other injury to th... --- Walk 2 --- [QF01.10] Acquired absence of female genital organs --RELATED_TO--> [?] Traumatic amputation of part of vulva --EXCLUDES--> [?] Female Genital Mutilation Def: A condition caused by procedures or other interventions for non-medical purposes. This condition is characterised by the partial or total removal of the external female genitalia or other injury to th... --- Walk 3 --- [9B73.3] Serous retinal detachment Def: This occurs due to inflammation, injury or vascular abnormalities that results in fluid accumulating underneath the retina without the presence of a hole, tear, or break.... --EXCLUDES--> [?] Central serous chorioretinopathy Def: This is an eye disease which causes visual impairment, often temporary, usually in one eye. When the disorder is active it is characterised by leakage of fluid under the retina that has a propensity t... --PARENT--> [?] Macular disorders --- Walk 4 --- [9B73.3] Serous retinal detachment Def: This occurs due to inflammation, injury or vascular abnormalities that results in fluid accumulating underneath the retina without the presence of a hole, tear, or break.... --PARENT--> [9B73] Retinal detachments or breaks Def: Retinal breaks are full thickness openings in the neurosensory retina that can be in the form of a hole, a tear or a retinal dialysis. Retinal detachment is a condition in which the retina peels away ... --CHILD--> [9B73.0] Retinal detachment with retinal break --- Walk 5 --- [JA8C.Z] Maternal care related to premature separation of placenta, unspecified --PARENT--> [JA8C] Maternal care related to premature separation of placenta --CHILD--> [JA8C.Z] Maternal care related to premature separation of placenta, unspecified --- Walk 6 --- [JA8C.Z] Maternal care related to premature separation of placenta, unspecified --PARENT--> [JA8C] Maternal care related to premature separation of placenta --CHILD--> [JA8C.Y] Other specified maternal care related to premature separation of placenta
[ "[QF01.10] Acquired absence of female genital organs\n --RELATED_TO--> [?] Traumatic amputation of entire vulva\n --EXCLUDES--> [?] Female Genital Mutilation\n Def: A condition caused by procedures or other interventions for non-medical purposes. This condition is characterised by the partial or total removal of the external female genitalia or other injury to th...", "[QF01.10] Acquired absence of female genital organs\n --RELATED_TO--> [?] Traumatic amputation of part of vulva\n --EXCLUDES--> [?] Female Genital Mutilation\n Def: A condition caused by procedures or other interventions for non-medical purposes. This condition is characterised by the partial or total removal of the external female genitalia or other injury to th...", "[9B73.3] Serous retinal detachment\n Def: This occurs due to inflammation, injury or vascular abnormalities that results in fluid accumulating underneath the retina without the presence of a hole, tear, or break....\n --EXCLUDES--> [?] Central serous chorioretinopathy\n Def: This is an eye disease which causes visual impairment, often temporary, usually in one eye. When the disorder is active it is characterised by leakage of fluid under the retina that has a propensity t...\n --PARENT--> [?] Macular disorders", "[9B73.3] Serous retinal detachment\n Def: This occurs due to inflammation, injury or vascular abnormalities that results in fluid accumulating underneath the retina without the presence of a hole, tear, or break....\n --PARENT--> [9B73] Retinal detachments or breaks\n Def: Retinal breaks are full thickness openings in the neurosensory retina that can be in the form of a hole, a tear or a retinal dialysis. Retinal detachment is a condition in which the retina peels away ...\n --CHILD--> [9B73.0] Retinal detachment with retinal break", "[JA8C.Z] Maternal care related to premature separation of placenta, unspecified\n --PARENT--> [JA8C] Maternal care related to premature separation of placenta\n --CHILD--> [JA8C.Z] Maternal care related to premature separation of placenta, unspecified", "[JA8C.Z] Maternal care related to premature separation of placenta, unspecified\n --PARENT--> [JA8C] Maternal care related to premature separation of placenta\n --CHILD--> [JA8C.Y] Other specified maternal care related to premature separation of placenta" ]
QF01.10
Acquired absence of female genital organs
[ { "from_icd11": "9B73.3", "icd10_code": "H3323", "icd10_title": "Serous retinal detachment, bilateral" }, { "from_icd11": "9B73.3", "icd10_code": "H3320", "icd10_title": "Serous retinal detachment, unspecified eye" }, { "from_icd11": "9B73.3", "icd10_code": "H3322", "icd10_title": "Serous retinal detachment, left eye" }, { "from_icd11": "9B73.3", "icd10_code": "H3321", "icd10_title": "Serous retinal detachment, right eye" }, { "from_icd11": "9B73.3", "icd10_code": "H332", "icd10_title": "Serous retinal detachment" }, { "from_icd11": "JA8C.Z", "icd10_code": "O4593", "icd10_title": "Premature separation of placenta, unspecified, third trimester" }, { "from_icd11": "JA8C.Z", "icd10_code": "O4592", "icd10_title": "Premature separation of placenta, unspecified, second trimester" }, { "from_icd11": "JA8C.Z", "icd10_code": "O458X3", "icd10_title": "Other premature separation of placenta, third trimester" }, { "from_icd11": "JA8C.Z", "icd10_code": "O458X2", "icd10_title": "Other premature separation of placenta, second trimester" }, { "from_icd11": "JA8C.Z", "icd10_code": "O4590", "icd10_title": "Premature separation of placenta, unspecified, unspecified trimester" }, { "from_icd11": "JA8C.Z", "icd10_code": "O458X1", "icd10_title": "Other premature separation of placenta, first trimester" }, { "from_icd11": "JA8C.Z", "icd10_code": "O4591", "icd10_title": "Premature separation of placenta, unspecified, first trimester" }, { "from_icd11": "JA8C.Z", "icd10_code": "O45", "icd10_title": "Premature separation of placenta [abruptio placentae]" }, { "from_icd11": "JA8C.Z", "icd10_code": "O458", "icd10_title": "Other premature separation of placenta" }, { "from_icd11": "JA8C.Z", "icd10_code": "O459", "icd10_title": "Premature separation of placenta, unspecified" } ]
H3323
Serous retinal detachment, bilateral
An endoscopic examination showed a broad, ulcerative lesion at 33cm to 38cm from the incisor that spanned more than three-fourths of the esophageal lumen circumference . The biopsy findings indicated moderately differentiated squamous cell carcinoma. Endoscopic ultrasonography (EUS) revealed a blurring and thickening of the third layer (submucosal layer). However, the fourth layer (proper muscle layer) was spared. In addition, we observed three malignant lymph nodes >10mm that were round in shape, had smooth features and exhibited hypoechogenicity. They were located 27cm, 28cm and 42cm from the incisor . However, we did not find any metastases on a computed tomography (CT) scan or a positron emission tomography (PET)-CT scan. Figure 1 Endoscopic examination. Esophageal cancer was observed at the middle to distal esophagus. It spanned more than three-fourths of the luminal circumference. (A) White light endoscopy. (B) Chemoendoscopy with iodine staining. After chemoradiotherapy, the lesion size decreased to approximately half of the circumference of the esophageal lumen. (C) White light endoscopy. (D) Chemoendoscopy with iodine staining. Figure 2 Endoscopic ultrasonography findings. (A) Blurring and thickening of the submucosal layer were observed, but the proper muscle layer was spared. Three enlarged regional lymph nodes (>10mm) were observed at 42cm (B) , 28cm (C) and 27cm (D) from the incisor.
3.900391
0.864258
sec[1]/p[1]
en
0.999996
25519497
https://doi.org/10.1186/1752-1947-8-439
[ "layer", "endoscopic", "three", "incisor", "esophageal", "circumference", "lesion", "that", "spanned", "fourths" ]
[ { "code": "9B78.6Z", "title": "Separation of retinal layers, unspecified" }, { "code": "9B78.6Y", "title": "Other specified separation of retinal layers" }, { "code": "JB09.0", "title": "First degree perineal laceration during delivery" }, { "code": "JB09.1", "title": "Second degree perineal laceration during delivery" }, { "code": "JB09.2", "title": "Third degree perineal laceration during delivery" }, { "code": "DA25.3Y/PK80.32", "title": "Oesophageal ulcer due to endoscopic procedures" }, { "code": "DA42.8Z/PK80.32", "title": "Gastritis due to endoscopic procedures" }, { "code": "DA51.5Y/PK80.32", "title": "Duodenitis due to endoscopic procedures" }, { "code": "PL11.4", "title": "Failure of sterile precautions, as mode of injury or harm" }, { "code": "PK80.92", "title": "Vascular procedure associated with injury or harm, endoscopic approach" } ]
=== ICD-11 CODES FOUND === [9B78.6Z] Separation of retinal layers, unspecified Also known as: Separation of retinal layers, unspecified | Separation of retinal layers | Detachment of retinal pigment epithelium | retinal pigment epithelial detachment [9B78.6Y] Other specified separation of retinal layers Also known as: Other specified separation of retinal layers [JB09.0] First degree perineal laceration during delivery Definition: Perineal lacerations involving the fourchette, perineal skin, and vaginal mucous membrane but not the underlying fascia and muscle. Also known as: First degree perineal laceration during delivery | first degree perineal laceration | laceration of superficial layers of perineal structures | obstetrical laceration, first degree | perineal obstetric rupture, first degree [JB09.1] Second degree perineal laceration during delivery Definition: Perineal lacerations involve, in addition, the fascia and muscles of the perineal body but not the anal sphincter. Also known as: Second degree perineal laceration during delivery | obstetrical laceration, second degree | second degree tear | Injury of pelvic floor complicating delivery | First degree perineal laceration, rupture or tear also involving the pelvic floor Excludes: that involving anal sphincter [JB09.2] Third degree perineal laceration during delivery Definition: Perineal lacerations extending farther to involve the anal sphincter. Also known as: Third degree perineal laceration during delivery | obstetrical laceration, third degree | third degree perineal laceration | third degree obstetric perineal rupture | third degree perineal laceration, with delivery Excludes: that involving anal or rectal mucosa [PL11.4] Failure of sterile precautions, as mode of injury or harm Definition: An infection occurred because standard procedures designed to minimize the risk of hospital acquired infection were not followed or were insufficient. Also known as: Failure of sterile precautions, as mode of injury or harm | failure of sterile precautions during intervention | contamination as mode of injury or harm | failure to take proper precautions | Failure of sterile precautions during surgical and medical care Excludes: Failure of sterile precautions without injury or harm [PK80.92] Vascular procedure associated with injury or harm, endoscopic approach Also known as: Vascular procedure associated with injury or harm, endoscopic approach Excludes: Circumstances associated with a surgical or other medical procedure influencing the episode of care, without injury or harm === GRAPH WALKS === --- Walk 1 --- [9B78.6Z] Separation of retinal layers, unspecified --PARENT--> [9B78.6] Separation of retinal layers --CHILD--> [9B78.60] Serous detachment of retinal pigment epithelium Def: This refers to the serous detachment of the pigmented cell layer just outside the neurosensory retina that nourishes retinal visual cells, and is firmly attached to the underlying choroid and overlyin... --- Walk 2 --- [9B78.6Z] Separation of retinal layers, unspecified --PARENT--> [9B78.6] Separation of retinal layers --PARENT--> [9B78] Certain specified retinal disorders --- Walk 3 --- [9B78.6Y] Other specified separation of retinal layers --PARENT--> [9B78.6] Separation of retinal layers --CHILD--> [9B78.6Y] Other specified separation of retinal layers --- Walk 4 --- [9B78.6Y] Other specified separation of retinal layers --PARENT--> [9B78.6] Separation of retinal layers --CHILD--> [9B78.6Y] Other specified separation of retinal layers --- Walk 5 --- [JB09.0] First degree perineal laceration during delivery Def: Perineal lacerations involving the fourchette, perineal skin, and vaginal mucous membrane but not the underlying fascia and muscle.... --PARENT--> [JB09] Perineal laceration during delivery Def: An injury characterised by a laceration to the maternal perineum during delivery.... --CHILD--> [JB09.1] Second degree perineal laceration during delivery Def: Perineal lacerations involve, in addition, the fascia and muscles of the perineal body but not the anal sphincter.... --- Walk 6 --- [JB09.0] First degree perineal laceration during delivery Def: Perineal lacerations involving the fourchette, perineal skin, and vaginal mucous membrane but not the underlying fascia and muscle.... --PARENT--> [JB09] Perineal laceration during delivery Def: An injury characterised by a laceration to the maternal perineum during delivery.... --CHILD--> [JB09.0] First degree perineal laceration during delivery Def: Perineal lacerations involving the fourchette, perineal skin, and vaginal mucous membrane but not the underlying fascia and muscle....
[ "[9B78.6Z] Separation of retinal layers, unspecified\n --PARENT--> [9B78.6] Separation of retinal layers\n --CHILD--> [9B78.60] Serous detachment of retinal pigment epithelium\n Def: This refers to the serous detachment of the pigmented cell layer just outside the neurosensory retina that nourishes retinal visual cells, and is firmly attached to the underlying choroid and overlyin...", "[9B78.6Z] Separation of retinal layers, unspecified\n --PARENT--> [9B78.6] Separation of retinal layers\n --PARENT--> [9B78] Certain specified retinal disorders", "[9B78.6Y] Other specified separation of retinal layers\n --PARENT--> [9B78.6] Separation of retinal layers\n --CHILD--> [9B78.6Y] Other specified separation of retinal layers", "[9B78.6Y] Other specified separation of retinal layers\n --PARENT--> [9B78.6] Separation of retinal layers\n --CHILD--> [9B78.6Y] Other specified separation of retinal layers", "[JB09.0] First degree perineal laceration during delivery\n Def: Perineal lacerations involving the fourchette, perineal skin, and vaginal mucous membrane but not the underlying fascia and muscle....\n --PARENT--> [JB09] Perineal laceration during delivery\n Def: An injury characterised by a laceration to the maternal perineum during delivery....\n --CHILD--> [JB09.1] Second degree perineal laceration during delivery\n Def: Perineal lacerations involve, in addition, the fascia and muscles of the perineal body but not the anal sphincter....", "[JB09.0] First degree perineal laceration during delivery\n Def: Perineal lacerations involving the fourchette, perineal skin, and vaginal mucous membrane but not the underlying fascia and muscle....\n --PARENT--> [JB09] Perineal laceration during delivery\n Def: An injury characterised by a laceration to the maternal perineum during delivery....\n --CHILD--> [JB09.0] First degree perineal laceration during delivery\n Def: Perineal lacerations involving the fourchette, perineal skin, and vaginal mucous membrane but not the underlying fascia and muscle...." ]
9B78.6Z
Separation of retinal layers, unspecified
[ { "from_icd11": "9B78.6Z", "icd10_code": "H35719", "icd10_title": "Central serous chorioretinopathy, unspecified eye" }, { "from_icd11": "9B78.6Z", "icd10_code": "H35711", "icd10_title": "Central serous chorioretinopathy, right eye" }, { "from_icd11": "9B78.6Z", "icd10_code": "H357", "icd10_title": "Separation of retinal layers" }, { "from_icd11": "JB09.0", "icd10_code": "O700", "icd10_title": "First degree perineal laceration during delivery" }, { "from_icd11": "JB09.1", "icd10_code": "O701", "icd10_title": "Second degree perineal laceration during delivery" }, { "from_icd11": "JB09.2", "icd10_code": "O7020", "icd10_title": "Third degree perineal laceration during delivery, unspecified" }, { "from_icd11": "JB09.2", "icd10_code": "O7021", "icd10_title": "Third degree perineal laceration during delivery, IIIa" }, { "from_icd11": "JB09.2", "icd10_code": "O7023", "icd10_title": "Third degree perineal laceration during delivery, IIIc" }, { "from_icd11": "JB09.2", "icd10_code": "O702", "icd10_title": "Third degree perineal laceration during delivery" }, { "from_icd11": "PL11.4", "icd10_code": "Y62", "icd10_title": "Failure of sterile precautions during surgical and medical care" }, { "from_icd11": "PL11.4", "icd10_code": "Y620", "icd10_title": "Failure of sterile precautions during surgical operation" }, { "from_icd11": "PL11.4", "icd10_code": "Y621", "icd10_title": "Failure of sterile precautions during infusion or transfusion" }, { "from_icd11": "PL11.4", "icd10_code": "Y622", "icd10_title": "Failure of sterile precautions during kidney dialysis and other perfusion" }, { "from_icd11": "PL11.4", "icd10_code": "Y623", "icd10_title": "Failure of sterile precautions during injection or immunization" }, { "from_icd11": "PL11.4", "icd10_code": "Y624", "icd10_title": "Failure of sterile precautions during endoscopic examination" } ]
H35719
Central serous chorioretinopathy, unspecified eye
At the age of 8 months he had purpura and gingival bleeding following a cold. Although WBC counts (8,300/μl) and hemoglobin levels (8.3 g/dl) were unchanged, platelet counts progressively decreased (13 × 10 3 /μl) again. Because a complication of ITP was most suspected, intravenous immunoglobulin (IVIG) (1 g/kg) and a dosage of steroid were administered to him. Unexpectedly, not only platelet counts but also hemoglobin levels (from 8.6 to 12.5 g/dl) quickly increased in association with decrement in reticulocytes and total bilirubin (from 626 to 229 × 10 3 /μl, from 4.5 to 1.9 mg/dl, respectively) in response to IVIG therapy. At that time, the percentage of reticulated platelets was 1.3% (reference value: <2%), and a level of thrombopoietin was normal (32 pg/mL, reference value: <142 pg/ml). Upshaw Schulman syndrome was excluded because of only slight low level of ADAMTS-13 activity (34.7%, reference value: 70-130%) and normal result of von Willebrand factor multimer analysis . Because the erythrocyte binding IgG quantitative analysis showed mild elevation in the patient, we concluded that the infant with HS was accompanied by ITP and DAT negative AIHA (Evans' syndrome). At the age of 10 months after confirming stability of platelet counts, tapering betamethasone resulted in gradually decreasing hemoglobin levels and platelet counts (hemoglobin 9 g/dl, platelets 3-5 × 10 3 /μl) as Figure 1 shown.
4.113281
0.942871
sec[1]/p[1]
en
0.999999
19740448
https://doi.org/10.1186/1756-8722-2-40
[ "counts", "hemoglobin", "platelet", "because", "reference", "ivig", "that", "platelets", "purpura", "gingival" ]
[ { "code": "3B63.1Z", "title": "Acquired thrombocytosis, unspecified" }, { "code": "3B64.Z", "title": "Thrombocytopenia, unspecified" }, { "code": "4B0Z", "title": "Immune system disorders involving white cell lineages, unspecified" }, { "code": "4B03.Z", "title": "Eosinophilia, unspecified" }, { "code": "4B00.1Z", "title": "Neutrophilia, unspecified" }, { "code": "3A51.1", "title": "Sickle cell disease without crisis" }, { "code": "3A51.Z", "title": "Sickle cell disorders or other haemoglobinopathies, unspecified" }, { "code": "MA18.4", "title": "Low haemoglobin" }, { "code": "3A50.4", "title": "Hereditary persistence of fetal haemoglobin" }, { "code": "3A51.A", "title": "Haemoglobin E disease" } ]
=== ICD-11 CODES FOUND === [3B63.1Z] Acquired thrombocytosis, unspecified Also known as: Acquired thrombocytosis, unspecified | Acquired thrombocytosis | Idiopathic haemorrhagic thrombocythaemia | Essential thrombocythaemia | primary haemorrhagic thrombocythaemia [3B64.Z] Thrombocytopenia, unspecified Also known as: Thrombocytopenia, unspecified | Thrombocytopenia | low platelet count | low platelets | decreased platelets [4B0Z] Immune system disorders involving white cell lineages, unspecified Also known as: Immune system disorders involving white cell lineages, unspecified [4B03.Z] Eosinophilia, unspecified Also known as: Eosinophilia, unspecified | Eosinophilia | Disorders with increased eosinophil counts | Idiopathic hypereosinophilic syndrome [4B00.1Z] Neutrophilia, unspecified Also known as: Neutrophilia, unspecified | Neutrophilia | Disorders with increased neutrophil counts [3A51.1] Sickle cell disease without crisis Definition: A disorder caused by a HbS mutation in the haemoglobin gene. This disorder is characterised by abnormal rigid sickle-shaped red blood cells decreasing its ability to carry oxygen. This disorder may present with fatigue, shortness of breath, dizziness, headaches, pallor of skin or mucous membranes, and jaundice. This disorder is confirmed by identification of HbS mutation by genetic testing. Also known as: Sickle cell disease without crisis | Hb-SS disease without crisis | HbSS without crisis | Sickle-cell anaemia without crisis | SCD - [sickle cell disease] [3A51.Z] Sickle cell disorders or other haemoglobinopathies, unspecified Also known as: Sickle cell disorders or other haemoglobinopathies, unspecified | Sickle cell disorders or other haemoglobinopathies | Sickle-cell disease or disorder with elliptocytosis | sickle-cell hemoglobin disease with elliptocytosis | sickle-cell elliptocytosis [MA18.4] Low haemoglobin Also known as: Low haemoglobin Excludes: Low affinity haemoglobin [3A50.4] Hereditary persistence of fetal haemoglobin Definition: Hereditary persistence of fetal haemoglobin (HPFH) associated with beta-thalassaemia is a haemoglobinopathy characterised by high haemoglobin (Hb)F levels and an increased number of fetal-Hb-containing cells. The association of HPFH with beta-thalassaemia mitigates the clinical manifestations which vary from a normal state to beta-thalassaemia intermedia. Also known as: Hereditary persistence of fetal haemoglobin | HPFH - [Hereditary persistence of fetal haemoglobin] | fetal haemoglobin | persistence of fetal haemoglobin | persistent haemoglobin F [3A51.A] Haemoglobin E disease Definition: Haemoglobin E disease is characterised by the synthesis of an abnormal haemoglobin called haemoglobin E (HbE), instead of the normal haemoglobin A (HbA). Subjects heterozygous for HbE (AE) have an asymptomatic condition with no clinical relevance, except for the risk of transmitting E/beta thalassemia if the other parent carries beta thalassemia. The severity of these E/beta thalassemia forms is very variable, the clinical picture ranging from that of beta thalassemia minor through to thalassemi Also known as: Haemoglobin E disease | Homozygous HbE carriers | Compound HbE or other Hb mutant heterozygotes === GRAPH WALKS === --- Walk 1 --- [3B63.1Z] Acquired thrombocytosis, unspecified --PARENT--> [3B63.1] Acquired thrombocytosis Def: A chronic myeloproliferative neoplasm that involves primarily the megakaryocytic lineage. It is characterised by sustained thrombocytosis in the blood, increased numbers of large, mature megakaryocyte... --PARENT--> [3B63] Thrombocytosis Def: A disease caused by essential thrombocytosis or other myelo-proliferative disorders such as chronic myelogenous leukaemia, polycythaemia, myelofibrosis. This disease can also have secondary causes suc... --- Walk 2 --- [3B63.1Z] Acquired thrombocytosis, unspecified --PARENT--> [3B63.1] Acquired thrombocytosis Def: A chronic myeloproliferative neoplasm that involves primarily the megakaryocytic lineage. It is characterised by sustained thrombocytosis in the blood, increased numbers of large, mature megakaryocyte... --PARENT--> [3B63] Thrombocytosis Def: A disease caused by essential thrombocytosis or other myelo-proliferative disorders such as chronic myelogenous leukaemia, polycythaemia, myelofibrosis. This disease can also have secondary causes suc... --- Walk 3 --- [3B64.Z] Thrombocytopenia, unspecified --PARENT--> [3B64] Thrombocytopenia Def: This disease is characterised by decreased levels of platelets within the blood. This disease may present with increased bruising or haemorrhaging. Confirmation is by identification of decreased plate... --CHILD--> [3B64.1] Acquired thrombocytopenia Def: A disease caused by determinants arising after birth, leading to low platelet count. This disease is characterised by low levels of platelets within the blood. This disease may present with increased ... --- Walk 4 --- [3B64.Z] Thrombocytopenia, unspecified --PARENT--> [3B64] Thrombocytopenia Def: This disease is characterised by decreased levels of platelets within the blood. This disease may present with increased bruising or haemorrhaging. Confirmation is by identification of decreased plate... --RELATED_TO--> [?] Isolated thrombocytopenia --- Walk 5 --- [4B0Z] Immune system disorders involving white cell lineages, unspecified --PARENT--> [?] Immune system disorders involving white cell lineages --RELATED_TO--> [?] Combined immunodeficiencies --- Walk 6 --- [4B0Z] Immune system disorders involving white cell lineages, unspecified --PARENT--> [?] Immune system disorders involving white cell lineages --CHILD--> [4B00] Disorders of neutrophil number
[ "[3B63.1Z] Acquired thrombocytosis, unspecified\n --PARENT--> [3B63.1] Acquired thrombocytosis\n Def: A chronic myeloproliferative neoplasm that involves primarily the megakaryocytic lineage. It is characterised by sustained thrombocytosis in the blood, increased numbers of large, mature megakaryocyte...\n --PARENT--> [3B63] Thrombocytosis\n Def: A disease caused by essential thrombocytosis or other myelo-proliferative disorders such as chronic myelogenous leukaemia, polycythaemia, myelofibrosis. This disease can also have secondary causes suc...", "[3B63.1Z] Acquired thrombocytosis, unspecified\n --PARENT--> [3B63.1] Acquired thrombocytosis\n Def: A chronic myeloproliferative neoplasm that involves primarily the megakaryocytic lineage. It is characterised by sustained thrombocytosis in the blood, increased numbers of large, mature megakaryocyte...\n --PARENT--> [3B63] Thrombocytosis\n Def: A disease caused by essential thrombocytosis or other myelo-proliferative disorders such as chronic myelogenous leukaemia, polycythaemia, myelofibrosis. This disease can also have secondary causes suc...", "[3B64.Z] Thrombocytopenia, unspecified\n --PARENT--> [3B64] Thrombocytopenia\n Def: This disease is characterised by decreased levels of platelets within the blood. This disease may present with increased bruising or haemorrhaging. Confirmation is by identification of decreased plate...\n --CHILD--> [3B64.1] Acquired thrombocytopenia\n Def: A disease caused by determinants arising after birth, leading to low platelet count. This disease is characterised by low levels of platelets within the blood. This disease may present with increased ...", "[3B64.Z] Thrombocytopenia, unspecified\n --PARENT--> [3B64] Thrombocytopenia\n Def: This disease is characterised by decreased levels of platelets within the blood. This disease may present with increased bruising or haemorrhaging. Confirmation is by identification of decreased plate...\n --RELATED_TO--> [?] Isolated thrombocytopenia", "[4B0Z] Immune system disorders involving white cell lineages, unspecified\n --PARENT--> [?] Immune system disorders involving white cell lineages\n --RELATED_TO--> [?] Combined immunodeficiencies", "[4B0Z] Immune system disorders involving white cell lineages, unspecified\n --PARENT--> [?] Immune system disorders involving white cell lineages\n --CHILD--> [4B00] Disorders of neutrophil number" ]
3B63.1Z
Acquired thrombocytosis, unspecified
[ { "from_icd11": "3B63.1Z", "icd10_code": "D473", "icd10_title": "Essential (hemorrhagic) thrombocythemia" }, { "from_icd11": "3B64.Z", "icd10_code": "D6942", "icd10_title": "Congenital and hereditary thrombocytopenia purpura" }, { "from_icd11": "3B64.Z", "icd10_code": "D6941", "icd10_title": "Evans syndrome" }, { "from_icd11": "3B64.Z", "icd10_code": "D6949", "icd10_title": "Other primary thrombocytopenia" }, { "from_icd11": "3B64.Z", "icd10_code": "D696", "icd10_title": "Thrombocytopenia, unspecified" }, { "from_icd11": "3B64.Z", "icd10_code": "D69", "icd10_title": "Purpura and other hemorrhagic conditions" }, { "from_icd11": "3B64.Z", "icd10_code": "D694", "icd10_title": "Other primary thrombocytopenia" }, { "from_icd11": "4B0Z", "icd10_code": "D72829", "icd10_title": "Elevated white blood cell count, unspecified" }, { "from_icd11": "4B0Z", "icd10_code": "D72819", "icd10_title": "Decreased white blood cell count, unspecified" }, { "from_icd11": "4B0Z", "icd10_code": "D72818", "icd10_title": "Other decreased white blood cell count" }, { "from_icd11": "4B0Z", "icd10_code": "D72828", "icd10_title": "Other elevated white blood cell count" }, { "from_icd11": "4B0Z", "icd10_code": "D72823", "icd10_title": "Leukemoid reaction" }, { "from_icd11": "4B0Z", "icd10_code": "D72821", "icd10_title": "Monocytosis (symptomatic)" }, { "from_icd11": "4B0Z", "icd10_code": "D72825", "icd10_title": "Bandemia" }, { "from_icd11": "4B0Z", "icd10_code": "D72810", "icd10_title": "Lymphocytopenia" } ]
D473
Essential (hemorrhagic) thrombocythemia
Between June 2009 and June 2010 36 consecutive patients received an esophageal resection due to esophageal cancer in our department. All patients underwent Ivor Lewis subtotal esophagectomy with two-field lymph node dissection. In brief, all resections were performed by initial abdominal exploration through an upper midline laparotomy. The stomach was mobilized on the right gastric and gastroepiploic arteries. The left gastric artery was divided at its origin, and all lymph nodes along the celiac axis and its three branches along the left aspect of the portal vein, in front of the inferior vena cava, along the diaphragmatic pillars were resected. A pyloromyotomy was not performed routinely. With a right anterolateral thoracotomy, the chest was entered through the fifth intercostal space. The azygos vein arch was divided, and the esophagus was dissected from esophagogastric junction to the apex of the chest. Complete lymph node dissection of the dorsal mediastinum including subcarinal lymph nodes was performed. A resection of the thoracic duct was not performed routinely. Denudation of the lesser curvature was usually performed in the pleural cavity. After resection of the specimen, an end-to-side anastomosis was constructed between the esophagus and the stomach. The anastomosis was located in the apex of the chest and was delivered by a circular stapler device. None of the patients were excluded.
3.96875
0.53418
sec[1]/p[1]
en
0.999998
22866813
https://doi.org/10.1186/1477-7819-10-159
[ "lymph", "patients", "resection", "along", "chest", "june", "esophageal", "node", "dissection", "stomach" ]
[ { "code": "BD9Z", "title": "Disorders of lymphatic vessels or lymph nodes, unspecified" }, { "code": "BD90.Z", "title": "Lymphadenitis, unspecified" }, { "code": "BD90.Y", "title": "Other specified lymphadenitis" }, { "code": "BD9Y", "title": "Other specified disorders of lymphatic vessels or lymph nodes" }, { "code": "MA01.Z", "title": "Enlarged lymph nodes, unspecified" }, { "code": "PL14.C", "title": "Patient received diagnostic test or treatment intended for another patient" }, { "code": "QB14", "title": "Unavailability or inaccessibility of health care facilities" }, { "code": "PL14.2", "title": "Problem associated with physical transfer of patient" }, { "code": "QB12.0", "title": "Organ transplant candidate" }, { "code": "QA15.1", "title": "Counselling related to sexual behaviour and orientation or sexual relationships of the person" } ]
=== ICD-11 CODES FOUND === [BD9Z] Disorders of lymphatic vessels or lymph nodes, unspecified Also known as: Disorders of lymphatic vessels or lymph nodes, unspecified | Lymphatic system disorders | lymph disease NOS | lymph gland disease | Lymphatic system disease NOS [BD90.Z] Lymphadenitis, unspecified Also known as: Lymphadenitis, unspecified | Lymphadenitis | adenitis NOS | inflammation of gland | lymphatic gland inflammation [BD90.Y] Other specified lymphadenitis Also known as: Other specified lymphadenitis | Dermatopathic lymphadenopathy | lipomelanotic reticulosis | Infective inguinal bubo | bubo [BD9Y] Other specified disorders of lymphatic vessels or lymph nodes Also known as: Other specified disorders of lymphatic vessels or lymph nodes | Chylous cyst | Mesentery chylous cyst | Peritoneum chylous cyst | Lymphocele [MA01.Z] Enlarged lymph nodes, unspecified Also known as: Enlarged lymph nodes, unspecified | Enlarged lymph nodes | swollen glands | Lymphadenopathy | adenopathy [PL14.C] Patient received diagnostic test or treatment intended for another patient Also known as: Patient received diagnostic test or treatment intended for another patient | wrong patient | incorrect patient Excludes: Procedure undertaken at wrong site or wrong side, as mode of injury or harm [QB14] Unavailability or inaccessibility of health care facilities Also known as: Unavailability or inaccessibility of health care facilities | unavailability of medical facilities | Unavailability of outpatient clinic | Unavailability or inaccessibility of residential aged care service Excludes: bed unavailable [PL14.2] Problem associated with physical transfer of patient Also known as: Problem associated with physical transfer of patient [QB12.0] Organ transplant candidate Also known as: Organ transplant candidate | patient waiting for organ availability | health services provided because of need for organ transplant | organ transplant candidate awaiting organ availability | person on organ transplant waiting list [QA15.1] Counselling related to sexual behaviour and orientation or sexual relationships of the person Also known as: Counselling related to sexual behaviour and orientation or sexual relationships of the person | advice on sexual behaviour or orientation | counselling on sexual behaviour or orientation | promiscuity counselling | patient concerned regarding sexual orientation === GRAPH WALKS === --- Walk 1 --- [BD9Z] Disorders of lymphatic vessels or lymph nodes, unspecified --PARENT--> [?] Disorders of lymphatic vessels or lymph nodes Def: Disorders due to developmental and acquired disturbances of lymph circulation and drainage and to infective disorders of lymph vessels and nodes.... --RELATED_TO--> [?] Lymphatic malformations Def: Lymphatic malformations (LM), formerly referred to by the term lymphangioma, are malformations of the lymphatic system which result in obstructed lymphatic drainage. There are two types of LM: macrocy... --- Walk 2 --- [BD9Z] Disorders of lymphatic vessels or lymph nodes, unspecified --PARENT--> [?] Disorders of lymphatic vessels or lymph nodes Def: Disorders due to developmental and acquired disturbances of lymph circulation and drainage and to infective disorders of lymph vessels and nodes.... --EXCLUDES--> [?] Enlarged lymph nodes Def: Enlarged lymph node is called lymphadenopathy which means the abnormal enlargement of lymph nodes.... --- Walk 3 --- [BD90.Z] Lymphadenitis, unspecified --PARENT--> [BD90] Lymphadenitis --CHILD--> [BD90.2] Chronic lymphadenitis --- Walk 4 --- [BD90.Z] Lymphadenitis, unspecified --PARENT--> [BD90] Lymphadenitis --EXCLUDES--> [?] Enlarged lymph nodes Def: Enlarged lymph node is called lymphadenopathy which means the abnormal enlargement of lymph nodes.... --- Walk 5 --- [BD90.Y] Other specified lymphadenitis --PARENT--> [BD90] Lymphadenitis --EXCLUDES--> [?] Human immunodeficiency virus disease Def: A case of HIV infection is defined as an individual with HIV infection irrespective of clinical stage including severe or stage 4 clinical disease (also known as AIDS) confirmed by laboratory criteria... --- Walk 6 --- [BD90.Y] Other specified lymphadenitis --PARENT--> [BD90] Lymphadenitis --CHILD--> [BD90.2] Chronic lymphadenitis
[ "[BD9Z] Disorders of lymphatic vessels or lymph nodes, unspecified\n --PARENT--> [?] Disorders of lymphatic vessels or lymph nodes\n Def: Disorders due to developmental and acquired disturbances of lymph circulation and drainage and to infective disorders of lymph vessels and nodes....\n --RELATED_TO--> [?] Lymphatic malformations\n Def: Lymphatic malformations (LM), formerly referred to by the term lymphangioma, are malformations of the lymphatic system which result in obstructed lymphatic drainage. There are two types of LM: macrocy...", "[BD9Z] Disorders of lymphatic vessels or lymph nodes, unspecified\n --PARENT--> [?] Disorders of lymphatic vessels or lymph nodes\n Def: Disorders due to developmental and acquired disturbances of lymph circulation and drainage and to infective disorders of lymph vessels and nodes....\n --EXCLUDES--> [?] Enlarged lymph nodes\n Def: Enlarged lymph node is called lymphadenopathy which means the abnormal enlargement of lymph nodes....", "[BD90.Z] Lymphadenitis, unspecified\n --PARENT--> [BD90] Lymphadenitis\n --CHILD--> [BD90.2] Chronic lymphadenitis", "[BD90.Z] Lymphadenitis, unspecified\n --PARENT--> [BD90] Lymphadenitis\n --EXCLUDES--> [?] Enlarged lymph nodes\n Def: Enlarged lymph node is called lymphadenopathy which means the abnormal enlargement of lymph nodes....", "[BD90.Y] Other specified lymphadenitis\n --PARENT--> [BD90] Lymphadenitis\n --EXCLUDES--> [?] Human immunodeficiency virus disease\n Def: A case of HIV infection is defined as an individual with HIV infection irrespective of clinical stage including severe or stage 4 clinical disease (also known as AIDS) confirmed by laboratory criteria...", "[BD90.Y] Other specified lymphadenitis\n --PARENT--> [BD90] Lymphadenitis\n --CHILD--> [BD90.2] Chronic lymphadenitis" ]
BD9Z
Disorders of lymphatic vessels or lymph nodes, unspecified
[ { "from_icd11": "BD9Z", "icd10_code": "I898", "icd10_title": "Other specified noninfective disorders of lymphatic vessels and lymph nodes" }, { "from_icd11": "BD9Z", "icd10_code": "I899", "icd10_title": "Noninfective disorder of lymphatic vessels and lymph nodes, unspecified" }, { "from_icd11": "BD9Z", "icd10_code": "I89", "icd10_title": "Other noninfective disorders of lymphatic vessels and lymph nodes" }, { "from_icd11": "BD90.Z", "icd10_code": "I889", "icd10_title": "Nonspecific lymphadenitis, unspecified" }, { "from_icd11": "BD90.Z", "icd10_code": "I88", "icd10_title": "Nonspecific lymphadenitis" }, { "from_icd11": "BD90.Z", "icd10_code": "I888", "icd10_title": "Other nonspecific lymphadenitis" }, { "from_icd11": "BD90.Z", "icd10_code": "L00-L08", "icd10_title": "" }, { "from_icd11": "MA01.Z", "icd10_code": "R599", "icd10_title": "Enlarged lymph nodes, unspecified" }, { "from_icd11": "MA01.Z", "icd10_code": "R59", "icd10_title": "Enlarged lymph nodes" }, { "from_icd11": "QB14", "icd10_code": "Z753", "icd10_title": "Unavailability and inaccessibility of health-care facilities" }, { "from_icd11": "QA15.1", "icd10_code": "F66", "icd10_title": "Other sexual disorders" }, { "from_icd11": "QA15.1", "icd10_code": "F660", "icd10_title": "" }, { "from_icd11": "QA15.1", "icd10_code": "F661", "icd10_title": "" }, { "from_icd11": "QA15.1", "icd10_code": "F662", "icd10_title": "" }, { "from_icd11": "QA15.1", "icd10_code": "F668", "icd10_title": "" } ]
I898
Other specified noninfective disorders of lymphatic vessels and lymph nodes
Hepatic portal venous gas (HPVG) was first described more than 55 years ago by Wolfe and Evans and was presented as a radiologic sign associated with more than 75% of mortality rate in infants with necrotizing enterocolitis (NEC) . Since that time, HPVG has been associated with numerous other underlying abdominal diseases, ranging from benign causes to potentially lethal diseases requiring prompt surgical intervention. Moreover, HPVG is recognized not as a specific disease entity but rather as a diagnostic clue in patients with acute abdominal pathology. Although early reports of HPVG estimated a mortality rate of 75% to 80%, more recent studies suggest mortality rates of 25% to 35% [ 3 – 5 ]. The observed reduction in mortality may be attributed to the increased availability of more sensitive diagnostic imaging modalities (i.e., ultrasonography (US) and computed tomography (CT)) that can detect even minute quantities of air in the portal system. In addition, there is also an increase in the proportion of nonfatal conditions reported with HPVG without associated mesenteric ischemia . We report a case of HPVG in a patient with Noonan's syndrome due to acute gastric dilatation in the setting of gastric outlet obstruction caused by a congenital band that is extremely rare in adults. This study reviews the clinical data in adults from the literature and discusses the management of underlying disease.
4.234375
0.712402
sec[0]/p[0]
en
0.999995
23819076
https://doi.org/10.1155/2013/723160
[ "hpvg", "mortality", "associated", "that", "portal", "underlying", "abdominal", "diseases", "gastric", "adults" ]
[ { "code": "MH14", "title": "Other ill-defined or unspecified causes of mortality" }, { "code": "PB6Z", "title": "Unspecified unintentional cause of morbidity or mortality" }, { "code": "PL2Z", "title": "External causes of morbidity or mortality, unspecified" }, { "code": "PB6Y", "title": "Other unintentional cause of morbidity or mortality" }, { "code": "PL2Y", "title": "Other specified external causes of morbidity or mortality" }, { "code": "MB25.02", "title": "Disorganised thinking" }, { "code": "LD2F.11", "title": "VATER association" }, { "code": "5A61.0", "title": "Hypopituitarism" }, { "code": "FB1Z", "title": "Conditions associated with the spine, unspecified" }, { "code": "QE5Z", "title": "Problems associated with relationships, unspecified" } ]
=== ICD-11 CODES FOUND === [MH14] Other ill-defined or unspecified causes of mortality Also known as: Other ill-defined or unspecified causes of mortality | death NOS | cause of mortality not stated | death of unknown cause | unknown cause of mortality Includes: unknown cause of mortality [PB6Z] Unspecified unintentional cause of morbidity or mortality Also known as: Unspecified unintentional cause of morbidity or mortality | Exposure to unspecified factor | Exposure to unspecified factor causing fracture | Exposure to unspecified factor causing other and unspecified injury | accidental cause NOS [PL2Z] External causes of morbidity or mortality, unspecified Also known as: External causes of morbidity or mortality, unspecified [PB6Y] Other unintentional cause of morbidity or mortality Also known as: Other unintentional cause of morbidity or mortality | Exposure to other and unspecified man-made environmental factors | Exposure to other specified factors | Contact with agricultural machinery | contact with animal-powered farm machine [PL2Y] Other specified external causes of morbidity or mortality Also known as: Other specified external causes of morbidity or mortality | Sequelae of external causes of morbidity and mortality | late effect of external causes of morbidity and mortality | Sequelae of transport accidents | late effect of transport accidents [MB25.02] Disorganised thinking Definition: A disturbance in the associative thought process typically manifested in speech in which the person shifts suddenly from one topic to another that is unrelated or minimally related to the first. The individual gives no indication of being aware of the disconnectedness or illogicality of their thinking. Also known as: Disorganised thinking | thought derailment | loose associations | disorganised speech [LD2F.11] VATER association Definition: VACTERL/VATER is an association of congenital malformations typically characterised by the presence of at least three of the following: vertebral defects, anal atresia, cardiac defects, tracheo-oesophageal fistula, renal anomalies, and limb abnormalities. Also known as: VATER association | VACTERL association [5A61.0] Hypopituitarism Definition: A disorder manifesting a deficiency or decrease of one or more pituitary hormones, which is caused by a variety of diseases such as tumour, trauma/surgery, irradiation, inflammation and haemorrhage/infarction. Also known as: Hypopituitarism | subpituitarism | hypophyseal dystrophy | hypohypophysism | anterior pituitary insufficiency (in part) Includes: pituitary cachexia | pituitary short stature [FB1Z] Conditions associated with the spine, unspecified Also known as: Conditions associated with the spine, unspecified | dorsopathies | disorder of spine | spinal disorder [QE5Z] Problems associated with relationships, unspecified Also known as: Problems associated with relationships, unspecified === GRAPH WALKS === --- Walk 1 --- [MH14] Other ill-defined or unspecified causes of mortality --PARENT--> [?] Ill-defined and unknown causes of mortality --EXCLUDES--> [?] Obstetric death of unspecified cause Def: A condition characterised by maternal death during pregnancy or within 42 days following delivery. This death may be associated with physiological, obstetrical, or other changes or is provoked by inte... --- Walk 2 --- [MH14] Other ill-defined or unspecified causes of mortality --PARENT--> [?] Ill-defined and unknown causes of mortality --EXCLUDES--> [?] Obstetric death of unspecified cause Def: A condition characterised by maternal death during pregnancy or within 42 days following delivery. This death may be associated with physiological, obstetrical, or other changes or is provoked by inte... --- Walk 3 --- [PB6Z] Unspecified unintentional cause of morbidity or mortality --PARENT--> [?] Unintentional causes --CHILD--> [?] Unintentional fall --- Walk 4 --- [PB6Z] Unspecified unintentional cause of morbidity or mortality --PARENT--> [?] Unintentional causes --CHILD--> [?] Unintentional transport injury event Def: !markdown [Definitions in relation to transport injury events] (https://icdcdn.who.int/icd11referenceguide/en/html/index.html#descriptions-related-to-transport-injury-events)... --- Walk 5 --- [PL2Z] External causes of morbidity or mortality, unspecified --PARENT--> [23] External causes of morbidity or mortality Def: !markdown The WHO definition of an ‘injury’ is: ‘Injuries are caused by acute exposure to physical agents such as mechanical energy, heat, electricity, chemicals, and ionizing radiation interacting wi... --CHILD--> [?] Assault --- Walk 6 --- [PL2Z] External causes of morbidity or mortality, unspecified --PARENT--> [23] External causes of morbidity or mortality Def: !markdown The WHO definition of an ‘injury’ is: ‘Injuries are caused by acute exposure to physical agents such as mechanical energy, heat, electricity, chemicals, and ionizing radiation interacting wi... --CHILD--> [?] Unintentional causes
[ "[MH14] Other ill-defined or unspecified causes of mortality\n --PARENT--> [?] Ill-defined and unknown causes of mortality\n --EXCLUDES--> [?] Obstetric death of unspecified cause\n Def: A condition characterised by maternal death during pregnancy or within 42 days following delivery. This death may be associated with physiological, obstetrical, or other changes or is provoked by inte...", "[MH14] Other ill-defined or unspecified causes of mortality\n --PARENT--> [?] Ill-defined and unknown causes of mortality\n --EXCLUDES--> [?] Obstetric death of unspecified cause\n Def: A condition characterised by maternal death during pregnancy or within 42 days following delivery. This death may be associated with physiological, obstetrical, or other changes or is provoked by inte...", "[PB6Z] Unspecified unintentional cause of morbidity or mortality\n --PARENT--> [?] Unintentional causes\n --CHILD--> [?] Unintentional fall", "[PB6Z] Unspecified unintentional cause of morbidity or mortality\n --PARENT--> [?] Unintentional causes\n --CHILD--> [?] Unintentional transport injury event\n Def: !markdown\n[Definitions in relation to transport injury events]\n(https://icdcdn.who.int/icd11referenceguide/en/html/index.html#descriptions-related-to-transport-injury-events)...", "[PL2Z] External causes of morbidity or mortality, unspecified\n --PARENT--> [23] External causes of morbidity or mortality\n Def: !markdown\nThe WHO definition of an ‘injury’ is: ‘Injuries are caused by acute exposure to physical agents such as mechanical energy, heat, electricity, chemicals, and ionizing radiation interacting wi...\n --CHILD--> [?] Assault", "[PL2Z] External causes of morbidity or mortality, unspecified\n --PARENT--> [23] External causes of morbidity or mortality\n Def: !markdown\nThe WHO definition of an ‘injury’ is: ‘Injuries are caused by acute exposure to physical agents such as mechanical energy, heat, electricity, chemicals, and ionizing radiation interacting wi...\n --CHILD--> [?] Unintentional causes" ]
MH14
Other ill-defined or unspecified causes of mortality
[ { "from_icd11": "MH14", "icd10_code": "R99", "icd10_title": "Ill-defined and unknown cause of mortality" }, { "from_icd11": "PB6Z", "icd10_code": "W312XXA", "icd10_title": "Contact with powered woodworking and forming machines, initial encounter" }, { "from_icd11": "PB6Z", "icd10_code": "W311XXA", "icd10_title": "Contact with metalworking machines, initial encounter" }, { "from_icd11": "PB6Z", "icd10_code": "W3189XA", "icd10_title": "Contact with other specified machinery, initial encounter" }, { "from_icd11": "PB6Z", "icd10_code": "W319XXS", "icd10_title": "Contact with unspecified machinery, sequela" }, { "from_icd11": "PB6Z", "icd10_code": "W3182XA", "icd10_title": "Contact with other commercial machinery, initial encounter" }, { "from_icd11": "PB6Z", "icd10_code": "W3182XS", "icd10_title": "Contact with other commercial machinery, sequela" }, { "from_icd11": "PB6Z", "icd10_code": "W3089XA", "icd10_title": "Contact with other specified agricultural machinery, initial encounter" }, { "from_icd11": "PB6Z", "icd10_code": "W309XXS", "icd10_title": "Contact with unspecified agricultural machinery, sequela" }, { "from_icd11": "PB6Z", "icd10_code": "W3089XS", "icd10_title": "Contact with other specified agricultural machinery, sequela" }, { "from_icd11": "PB6Z", "icd10_code": "W310XXA", "icd10_title": "Contact with mining and earth-drilling machinery, initial encounter" }, { "from_icd11": "PB6Z", "icd10_code": "W3183XA", "icd10_title": "Contact with special construction vehicle in stationary use, initial encounter" }, { "from_icd11": "PB6Z", "icd10_code": "W3183XD", "icd10_title": "Contact with special construction vehicle in stationary use, subsequent encounter" }, { "from_icd11": "PB6Z", "icd10_code": "W319XXA", "icd10_title": "Contact with unspecified machinery, initial encounter" }, { "from_icd11": "PB6Z", "icd10_code": "W312XXS", "icd10_title": "Contact with powered woodworking and forming machines, sequela" } ]
R99
Ill-defined and unknown cause of mortality
A 16 month-old girl was evaluated for DD and seizures. She was born at 37 weeks of gestation by spontaneous delivery after an uneventful pregnancy. Neonatal weight was 2.49 kg (25 th percentile), length 47.8 cm (25 th percentile), head circumference 32.2 cm (3 rd percentile). APGAR scores were 9 at the first and fifth minute. At birth, a ventricular septal defect (VSD) and a bicuspid aortic valve were detected by ecochardiogram. She was able to sit alone at 7 months, but indipendent walking was still not achieved at 16 months. At 10 months she presented generalized seizures characterized by gaze, circumoral cyanosis, masticatory movements. Right temporal spike and wave activity, associated with irritative multifocal anomalies were recorded on EEG; even if valproic acid therapy was subsequently undertaken, EEG anomalies persisted for 1 year and the children experienced febrile seizures during the second year of life. Moreover, external hydrocephalus was detected by MRI. On physical examination at 16 months, weight was 10.3 kg (10 th –25 th percentile), head circumference 47 cm (50 th percentile), length 80 cm (50 th percentile); straight eyebrows, deep set eyes and divergent strabismus were noted. Ophtalmological examination revealed bilateral nystagmus and hypermetropic astigmatism. Subtelomeric FISH analysis revealed a de novo terminal deletion of chromosome 1p (46, XX, ish.del (1p)(pVYS218C-)).
4.046875
0.979004
sec[2]/sec[1]/p[0]
en
0.999997
19490664
https://doi.org/10.1186/1824-7288-35-9
[ "percentile", "seizures", "weight", "length", "head", "circumference", "anomalies", "girl", "evaluated", "born" ]
[ { "code": "5B81.00", "title": "Obesity in children or adolescents" }, { "code": "8A68.Z", "title": "Type of seizure, unspecified" }, { "code": "8A6Z", "title": "Epilepsy or seizures, unspecified" }, { "code": "8A63.Y", "title": "Seizure due to other acute cause" }, { "code": "8A67", "title": "Acute repetitive seizures" }, { "code": "8A68.Y", "title": "Other specified type of seizure" }, { "code": "MG43.5", "title": "Excessive weight loss" }, { "code": "MG43.6", "title": "Excessive weight gain" }, { "code": "MG44.11", "title": "Failure to thrive in infant or child" }, { "code": "5B80.0Z", "title": "Overweight, unspecified" } ]
=== ICD-11 CODES FOUND === [5B81.00] Obesity in children or adolescents Definition: In infants, children and adolescents, BMI categories for defining obesity vary by age and gender based on WHO growth charts. Children 0 to 5 years have obesity if weight-for-length/height or BMI-for-age is above 3 standard deviations of the median of the WHO Child Growth Standards. Children aged 5 to 19 years have obesity if BMI-for-age is above 2 standard deviations of the median of WHO Growth Reference for School-aged Children and Adolescents. Also known as: Obesity in children or adolescents | morbid obesity in children or adolescents | BMI-for age -[body mass index-for-age] percentile greater than 95 percent | Obesity in infants or children up to 5 years of age | Obesity in school-aged children or adolescents from 5 to 19 years [8A68.Z] Type of seizure, unspecified Also known as: Type of seizure, unspecified | Types of seizures | uncontrolled seizures | Seizure NOS | fits NOS [8A6Z] Epilepsy or seizures, unspecified Also known as: Epilepsy or seizures, unspecified | Cerebral seizures | Seizure disorder | seizure disorder, so described | epilepsy NOS [8A63.Y] Seizure due to other acute cause Also known as: Seizure due to other acute cause | Seizures due to immune disorders | Seizures due to medications | Toxic syndrome with generalised seizures, drug related | Acute seizures due to central nervous system infections or infestations [8A67] Acute repetitive seizures Definition: Acute repetitive seizures are multiple seizures, with a distinct time of onset, with recovery between each seizure, occurring within 24 hours in adults, or 12 hours in children. Also known as: Acute repetitive seizures | complex partial status epilepticus | Cluster seizures | Serial seizures | Recurrent seizures [8A68.Y] Other specified type of seizure Also known as: Other specified type of seizure | Absence episode | Absence seizure episode | Pseudotetanus | Clonic seizure disorder [MG43.5] Excessive weight loss Definition: A reduction of total body mass, due to loss of fluid, body fat or adipose tissue, or lean (muscle) mass that is sufficient in quantity or rate to create risk to the individual’s health. Also known as: Excessive weight loss | abnormal decrease in weight | abnormal weight loss | unintended weight loss | weight loss NOS [MG43.6] Excessive weight gain Definition: An increase in total body mass, due to increase in fluid, fat or adipose tissue, or lean (muscle) mass that is outside the expected range for normal growth and development and is sufficient in quantity or rate to create risk to the individual’s health. Also known as: Excessive weight gain | abnormal increase in weight | abnormal weight gain | unintended weight gain Excludes: Obesity [MG44.11] Failure to thrive in infant or child Definition: When an infant or child's current weight or rate of weight gain is significantly below that of other children of similar age and gender. Also known as: Failure to thrive in infant or child | failure to gain weight | failure to thrive NOS | FTT - [failure to thrive] syndrome Excludes: Failure to thrive in newborn | Anorexia Nervosa | Avoidant-restrictive food intake disorder [5B80.0Z] Overweight, unspecified Also known as: Overweight, unspecified | Overweight === GRAPH WALKS === --- Walk 1 --- [5B81.00] Obesity in children or adolescents Def: In infants, children and adolescents, BMI categories for defining obesity vary by age and gender based on WHO growth charts. Children 0 to 5 years have obesity if weight-for-length/height or BMI-for-a... --PARENT--> [5B81.0] Obesity due to energy imbalance Def: Obesity is a chronic complex disease defined by excessive adiposity that can impair health. It is in most cases a multifactorial disease due to obesogenic environments, psycho-social factors and genet... --CHILD--> [5B81.00] Obesity in children or adolescents Def: In infants, children and adolescents, BMI categories for defining obesity vary by age and gender based on WHO growth charts. Children 0 to 5 years have obesity if weight-for-length/height or BMI-for-a... --- Walk 2 --- [5B81.00] Obesity in children or adolescents Def: In infants, children and adolescents, BMI categories for defining obesity vary by age and gender based on WHO growth charts. Children 0 to 5 years have obesity if weight-for-length/height or BMI-for-a... --PARENT--> [5B81.0] Obesity due to energy imbalance Def: Obesity is a chronic complex disease defined by excessive adiposity that can impair health. It is in most cases a multifactorial disease due to obesogenic environments, psycho-social factors and genet... --CHILD--> [5B81.01] Obesity in adults Def: Obesity is defined as a body mass index (BMI) greater than or equal to 30.00 kg/m². There are three levels of severity in recognition of different management options.... --- Walk 3 --- [8A68.Z] Type of seizure, unspecified --PARENT--> [8A68] Types of seizures --CHILD--> [8A68.1] Absence seizures, atypical Def: Absence seizures with changes in tone more pronounced than in typical absences or with non-abrupt onset and/or cessation, often associated with slow, irregular, generalised spike-wave activity.... --- Walk 4 --- [8A68.Z] Type of seizure, unspecified --PARENT--> [8A68] Types of seizures --CHILD--> [8A68.1] Absence seizures, atypical Def: Absence seizures with changes in tone more pronounced than in typical absences or with non-abrupt onset and/or cessation, often associated with slow, irregular, generalised spike-wave activity.... --- Walk 5 --- [8A6Z] Epilepsy or seizures, unspecified --PARENT--> [?] Epilepsy or seizures Def: At least 2 unprovoked (or reflex) seizures occurring more than 24 hours apart.... --CHILD--> [8A60] Epilepsy due to structural or metabolic conditions or diseases Def: Epilepsy occurring in relation to a distinct other structural or metabolic condition or disease that has been demonstrated to be associated with a substantially increased risk of developing epilepsy.... --- Walk 6 --- [8A6Z] Epilepsy or seizures, unspecified --PARENT--> [?] Epilepsy or seizures Def: At least 2 unprovoked (or reflex) seizures occurring more than 24 hours apart.... --CHILD--> [8A60] Epilepsy due to structural or metabolic conditions or diseases Def: Epilepsy occurring in relation to a distinct other structural or metabolic condition or disease that has been demonstrated to be associated with a substantially increased risk of developing epilepsy....
[ "[5B81.00] Obesity in children or adolescents\n Def: In infants, children and adolescents, BMI categories for defining obesity vary by age and gender based on WHO growth charts. Children 0 to 5 years have obesity if weight-for-length/height or BMI-for-a...\n --PARENT--> [5B81.0] Obesity due to energy imbalance\n Def: Obesity is a chronic complex disease defined by excessive adiposity that can impair health. It is in most cases a multifactorial disease due to obesogenic environments, psycho-social factors and genet...\n --CHILD--> [5B81.00] Obesity in children or adolescents\n Def: In infants, children and adolescents, BMI categories for defining obesity vary by age and gender based on WHO growth charts. Children 0 to 5 years have obesity if weight-for-length/height or BMI-for-a...", "[5B81.00] Obesity in children or adolescents\n Def: In infants, children and adolescents, BMI categories for defining obesity vary by age and gender based on WHO growth charts. Children 0 to 5 years have obesity if weight-for-length/height or BMI-for-a...\n --PARENT--> [5B81.0] Obesity due to energy imbalance\n Def: Obesity is a chronic complex disease defined by excessive adiposity that can impair health. It is in most cases a multifactorial disease due to obesogenic environments, psycho-social factors and genet...\n --CHILD--> [5B81.01] Obesity in adults\n Def: Obesity is defined as a body mass index (BMI) greater than or equal to 30.00 kg/m². There are three levels of severity in recognition of different management options....", "[8A68.Z] Type of seizure, unspecified\n --PARENT--> [8A68] Types of seizures\n --CHILD--> [8A68.1] Absence seizures, atypical\n Def: Absence seizures with changes in tone more pronounced than in typical absences or with non-abrupt onset and/or cessation, often associated with slow, irregular, generalised spike-wave activity....", "[8A68.Z] Type of seizure, unspecified\n --PARENT--> [8A68] Types of seizures\n --CHILD--> [8A68.1] Absence seizures, atypical\n Def: Absence seizures with changes in tone more pronounced than in typical absences or with non-abrupt onset and/or cessation, often associated with slow, irregular, generalised spike-wave activity....", "[8A6Z] Epilepsy or seizures, unspecified\n --PARENT--> [?] Epilepsy or seizures\n Def: At least 2 unprovoked (or reflex) seizures occurring more than 24 hours apart....\n --CHILD--> [8A60] Epilepsy due to structural or metabolic conditions or diseases\n Def: Epilepsy occurring in relation to a distinct other structural or metabolic condition or disease that has been demonstrated to be associated with a substantially increased risk of developing epilepsy....", "[8A6Z] Epilepsy or seizures, unspecified\n --PARENT--> [?] Epilepsy or seizures\n Def: At least 2 unprovoked (or reflex) seizures occurring more than 24 hours apart....\n --CHILD--> [8A60] Epilepsy due to structural or metabolic conditions or diseases\n Def: Epilepsy occurring in relation to a distinct other structural or metabolic condition or disease that has been demonstrated to be associated with a substantially increased risk of developing epilepsy...." ]
5B81.00
Obesity in children or adolescents
[ { "from_icd11": "8A68.Z", "icd10_code": "R561", "icd10_title": "Post traumatic seizures" }, { "from_icd11": "8A68.Z", "icd10_code": "R569", "icd10_title": "Unspecified convulsions" }, { "from_icd11": "8A68.Z", "icd10_code": "R56", "icd10_title": "Convulsions, not elsewhere classified" }, { "from_icd11": "8A68.Z", "icd10_code": "R568", "icd10_title": "" }, { "from_icd11": "8A6Z", "icd10_code": "G40A09", "icd10_title": "Absence epileptic syndrome, not intractable, without status epilepticus" }, { "from_icd11": "8A6Z", "icd10_code": "G40B09", "icd10_title": "Juvenile myoclonic epilepsy, not intractable, without status epilepticus" }, { "from_icd11": "8A6Z", "icd10_code": "G40B19", "icd10_title": "Juvenile myoclonic epilepsy, intractable, without status epilepticus" }, { "from_icd11": "8A6Z", "icd10_code": "G40A19", "icd10_title": "Absence epileptic syndrome, intractable, without status epilepticus" }, { "from_icd11": "8A6Z", "icd10_code": "G40A11", "icd10_title": "Absence epileptic syndrome, intractable, with status epilepticus" }, { "from_icd11": "8A6Z", "icd10_code": "G40A01", "icd10_title": "Absence epileptic syndrome, not intractable, with status epilepticus" }, { "from_icd11": "8A6Z", "icd10_code": "G40409", "icd10_title": "Other generalized epilepsy and epileptic syndromes, not intractable, without status epilepticus" }, { "from_icd11": "8A6Z", "icd10_code": "G40802", "icd10_title": "Other epilepsy, not intractable, without status epilepticus" }, { "from_icd11": "8A6Z", "icd10_code": "G40801", "icd10_title": "Other epilepsy, not intractable, with status epilepticus" }, { "from_icd11": "8A6Z", "icd10_code": "G40901", "icd10_title": "Epilepsy, unspecified, not intractable, with status epilepticus" }, { "from_icd11": "8A6Z", "icd10_code": "G4089", "icd10_title": "Other seizures" } ]
R561
Post traumatic seizures
3 patients (5%) subsequently underwent lumbar fusion for increasing back pain despite good relief of radicular symptoms after endoscopic discectomy. One of these patients was a 25 year old male who presented initially with left L4 radicular symptoms. MRI showed L4L5 and L5S1 degenerate discs with a left L4L5 prolapsed intervetebral disc. A left L4L5 endoscopic discectomy was initially performed for him but on followup, he complained of increasing back pain and had L4L5, L5S1 transforaminal lumbar interbody fusion done 3 months after endoscopic discectomy. Another was a 45 year old male who had right L5 radicular symptoms and back pain preoperatively. MRI showed a right L5S1 posterolateral disc prolapse. He underwent right L5S1 endoscopic discectomy but also had increasing back pain on followup. He eventually had L5S1 posterior lumbar interbody fusion done 7 months post-edoscopic discectomy. For both of these patients, their initial radicular symptoms resolved after endoscopic discectomy. The third patient was a 36 year old female with left L4 radicular pain. MRI showed a L4L5 prolapsed disc. Post- endoscopic discectomy, her radicular sumptoms resolved. However 3 years postoperation, she complained of back pain and left L4 radicular pain again. Postoperation MRI showed diffuse L45 disc bulge and central and lateral recess stenosis. She subsequently underwent transforaminal lumbar interbody fusion.
3.876953
0.922852
sec[2]/p[3]
en
0.999997
19555483
https://doi.org/10.1186/1749-799X-4-20
[ "pain", "radicular", "discectomy", "endoscopic", "back", "lumbar", "fusion", "disc", "patients", "increasing" ]
[ { "code": "MG3Z", "title": "Pain, unspecified" }, { "code": "8E43.Z", "title": "Pain disorders, unspecified" }, { "code": "MG31.Z", "title": "Acute pain, unspecified" }, { "code": "MG30.Z", "title": "Chronic pain, unspecified" }, { "code": "FB56.2", "title": "Myalgia" }, { "code": "8B93.Z", "title": "Radiculopathy, unspecified" }, { "code": "DA09.8", "title": "Radicular cyst" }, { "code": "MG30.51", "title": "Chronic peripheral neuropathic pain" }, { "code": "8B93.Y", "title": "Other specified radiculopathy" }, { "code": "2E83.1", "title": "Benign osteogenic tumours of bone or articular cartilage of lower jaw" } ]
=== ICD-11 CODES FOUND === [MG3Z] Pain, unspecified Also known as: Pain, unspecified | pain observations | pain NOS | generalised pain | generalised pain, NOS [8E43.Z] Pain disorders, unspecified Also known as: Pain disorders, unspecified | Pain disorders [MG31.Z] Acute pain, unspecified Also known as: Acute pain, unspecified | Acute pain [MG30.Z] Chronic pain, unspecified Also known as: Chronic pain, unspecified | Chronic pain [FB56.2] Myalgia Definition: This is a disorder characterised by pain in a muscle or group of muscles. Also known as: Myalgia | muscle ache | muscle soreness | muscular pain | myalgic Excludes: Chronic primary musculoskeletal pain | Chronic secondary musculoskeletal pain [8B93.Z] Radiculopathy, unspecified Also known as: Radiculopathy, unspecified | Radiculopathy | radiculopathy, site unspecified | radicular neuropathy | radicular syndrome [DA09.8] Radicular cyst Definition: The radicular cyst is defined as an area of chronic inflammation exhibiting a closed central cavity surrounded by an epithelial lining. Also known as: Radicular cyst | apical cyst | apical radicular cyst | periradicular cyst | radiculodental cyst Excludes: lateral periodontal cyst [MG30.51] Chronic peripheral neuropathic pain Definition: Chronic peripheral neuropathic pain is chronic pain caused by a lesion or disease of the peripheral somatosensory nervous system. The pain may be spontaneous or evoked, as an increased response to a painful stimulus (hyperalgesia) or a painful response to a normally nonpainful stimulus (allodynia). The diagnosis of peripheral neuropathic pain requires a history of peripheral nervous system injury or disease and a neuroanatomically plausible distribution of the pain. Negative (e.g., decreased or Also known as: Chronic peripheral neuropathic pain | Chronic neuropathic pain after peripheral nerve injury | Chronic painful polyneuropathy | Chronic painful polyneuropathy associated with Human Immunodeficiency Virus infection | Chronic painful polyneuropathy associated with HIV - [Human immunodeficiency virus] infection Includes: Chronic neuropathic pain after peripheral nerve injury | Chronic painful polyneuropathy | Chronic painful radiculopathy [8B93.Y] Other specified radiculopathy Also known as: Other specified radiculopathy | Radiculopathy, multiple sites in spine | Radiculopathy, occipito-atlanto-axial region | Radiculopathy, cervical region | Radiculopathy, cervicothoracic region [2E83.1] Benign osteogenic tumours of bone or articular cartilage of lower jaw Also known as: Benign osteogenic tumours of bone or articular cartilage of lower jaw | benign neoplasm of mandible | Adenoameloblastoma of lower jaw | adenoameloblastoma of unspecified site | Adenomatoid odontogenic tumour of lower jaw === GRAPH WALKS === --- Walk 1 --- [MG3Z] Pain, unspecified --PARENT--> [?] Pain --EXCLUDES--> [?] Headache disorders --- Walk 2 --- [MG3Z] Pain, unspecified --PARENT--> [?] Pain --EXCLUDES--> [?] Headache disorders --- Walk 3 --- [8E43.Z] Pain disorders, unspecified --PARENT--> [8E43] Pain disorders --CHILD--> [8E43.0] Neuropathic pain Def: Neuropathic pain is described as electric, burning, or shock like, caused by metabolic, nutritional, infectious, genetic, autoimmune, and/or vasculitic processes. The pain may occur spontaneously, wit... --- Walk 4 --- [8E43.Z] Pain disorders, unspecified --PARENT--> [8E43] Pain disorders --CHILD--> [8E43.Z] Pain disorders, unspecified --- Walk 5 --- [MG31.Z] Acute pain, unspecified --PARENT--> [MG31] Acute pain Def: Pain with a duration of less than 3 months. This code should be used only when there is no further specification of site.... --CHILD--> [MG31.2] Acute postoperative pain, not elsewhere classified Def: Pain at the intervention site or caused by an intervention.... --- Walk 6 --- [MG31.Z] Acute pain, unspecified --PARENT--> [MG31] Acute pain Def: Pain with a duration of less than 3 months. This code should be used only when there is no further specification of site.... --CHILD--> [MG31.2] Acute postoperative pain, not elsewhere classified Def: Pain at the intervention site or caused by an intervention....
[ "[MG3Z] Pain, unspecified\n --PARENT--> [?] Pain\n --EXCLUDES--> [?] Headache disorders", "[MG3Z] Pain, unspecified\n --PARENT--> [?] Pain\n --EXCLUDES--> [?] Headache disorders", "[8E43.Z] Pain disorders, unspecified\n --PARENT--> [8E43] Pain disorders\n --CHILD--> [8E43.0] Neuropathic pain\n Def: Neuropathic pain is described as electric, burning, or shock like, caused by metabolic, nutritional, infectious, genetic, autoimmune, and/or vasculitic processes. The pain may occur spontaneously, wit...", "[8E43.Z] Pain disorders, unspecified\n --PARENT--> [8E43] Pain disorders\n --CHILD--> [8E43.Z] Pain disorders, unspecified", "[MG31.Z] Acute pain, unspecified\n --PARENT--> [MG31] Acute pain\n Def: Pain with a duration of less than 3 months.\n\nThis code should be used only when there is no further specification of site....\n --CHILD--> [MG31.2] Acute postoperative pain, not elsewhere classified\n Def: Pain at the intervention site or caused by an intervention....", "[MG31.Z] Acute pain, unspecified\n --PARENT--> [MG31] Acute pain\n Def: Pain with a duration of less than 3 months.\n\nThis code should be used only when there is no further specification of site....\n --CHILD--> [MG31.2] Acute postoperative pain, not elsewhere classified\n Def: Pain at the intervention site or caused by an intervention...." ]
MG3Z
Pain, unspecified
[ { "from_icd11": "MG3Z", "icd10_code": "R52", "icd10_title": "Pain, unspecified" }, { "from_icd11": "MG3Z", "icd10_code": "R529", "icd10_title": "" }, { "from_icd11": "MG31.Z", "icd10_code": "R520", "icd10_title": "" }, { "from_icd11": "MG30.Z", "icd10_code": "R521", "icd10_title": "" }, { "from_icd11": "MG30.Z", "icd10_code": "R522", "icd10_title": "" }, { "from_icd11": "FB56.2", "icd10_code": "M7918", "icd10_title": "Myalgia, other site" }, { "from_icd11": "FB56.2", "icd10_code": "M7910", "icd10_title": "Myalgia, unspecified site" }, { "from_icd11": "FB56.2", "icd10_code": "M7912", "icd10_title": "Myalgia of auxiliary muscles, head and neck" }, { "from_icd11": "FB56.2", "icd10_code": "M791", "icd10_title": "Myalgia" }, { "from_icd11": "8B93.Z", "icd10_code": "M4726", "icd10_title": "Other spondylosis with radiculopathy, lumbar region" }, { "from_icd11": "8B93.Z", "icd10_code": "M4722", "icd10_title": "Other spondylosis with radiculopathy, cervical region" }, { "from_icd11": "8B93.Z", "icd10_code": "M5417", "icd10_title": "Radiculopathy, lumbosacral region" }, { "from_icd11": "8B93.Z", "icd10_code": "M4724", "icd10_title": "Other spondylosis with radiculopathy, thoracic region" }, { "from_icd11": "8B93.Z", "icd10_code": "M5414", "icd10_title": "Radiculopathy, thoracic region" }, { "from_icd11": "8B93.Z", "icd10_code": "M5418", "icd10_title": "Radiculopathy, sacral and sacrococcygeal region" } ]
R52
Pain, unspecified
From the above-given laboratory reports and investigations, it was clear that the patient was suffering from Patau syndrome with congenital heart defects as echocardiography revealed clear findings. Moreover, visible dysmorphic features were observed on the patient body, such as the cleft palate, low set ears, cleft lip, and right club foot. This Echocardiography report and physical examination findings verified the ultimate diagnosis as Patau syndrome associated with congenital heart defects. On confirmation of diagnosis, the patient was transferred to the nursery ward. As a result of this diagnosis, the patient's first care strategy included oxygen administration to increase the oxygen saturation of the patient. Additionally, a nasogastric tube was passed, and the patient was given a feed every 5 seconds per 2 h. He was given IV Claforan 125mg twice a day, IV Ampicillin 125 mg two times a day, IV Lasix 5mg twice a day, and oral tablet Capril 1 cc, Tablet Aldactone 1 cc. The patient was also given 10 percent dextrose water 11ml/hr continuously. This medication administration was continued till the next day. On next day, IV Claforan, IV Ampicillin, and IV Lasix were given thrice a day. While tablet Capril, Tablet Aldactone, were given two times a day. The patient surgical plan of care included pulmonary binding, PDA ligation, VSD closure, and repair of ASA with disbanding of the pulmonary artery.
3.583984
0.984375
sec[1]/p[4]
en
0.999997
PMC9422041
https://doi.org/10.1016/j.amsu.2022.104100
[ "tablet", "this", "clear", "patau", "congenital", "heart", "defects", "echocardiography", "cleft", "included" ]
[ { "code": "NE60", "title": "Harmful effects of drugs, medicaments or biological substances, not elsewhere classified" }, { "code": "PL00", "title": "Drugs, medicaments or biological substances associated with injury or harm in therapeutic use" }, { "code": "PL13.1", "title": "Underdosing, as mode of injury or harm" }, { "code": "PL13.0", "title": "Overdose of substance, as mode of injury or harm" }, { "code": "4A01.03", "title": "Transient hypogammaglobulinaemia of infancy" }, { "code": "2F21.Y", "title": "Other specified benign keratinocytic acanthomas" }, { "code": "2C73.00", "title": "Clear cell adenocarcinoma of ovary" }, { "code": "2D12.1", "title": "Adenocarcinoma of other endocrine glands or related structures" }, { "code": "2C25.Y", "title": "Other specified malignant neoplasms of bronchus or lung" }, { "code": "2C25.2", "title": "Squamous cell carcinoma of bronchus or lung" } ]
=== ICD-11 CODES FOUND === [NE60] Harmful effects of drugs, medicaments or biological substances, not elsewhere classified Also known as: Harmful effects of drugs, medicaments or biological substances, not elsewhere classified | drugs, medicaments or biological substances, toxicity not elsewhere classified | adverse drug effects | drug reaction NOS | drug allergy NOS Excludes: Alcohol intoxication | pathological drug intoxication | hypersensitivity reaction to correctly administered drug [PL00] Drugs, medicaments or biological substances associated with injury or harm in therapeutic use Also known as: Drugs, medicaments or biological substances associated with injury or harm in therapeutic use | Drugs medicaments or biological substances associated with injury or harm in therapeutic use, Systemic antibiotics | Drugs medicaments or biological substances associated with injury or harm in therapeutic use, Systemic antibiotics, Penicillins | Drugs medicaments or biological substances associated with injury or harm in therapeutic use, Systemic antibiotics, Cephalosporins or other beta-lactam antibiotics | Drugs medicaments or biological substances associated with injury or harm in therapeutic use, Systemic antibiotics, Chloramphenicol group Excludes: Circumstances associated with exposure to a drug, medicament or biological substance influencing the episode of care without injury or harm [PL13.1] Underdosing, as mode of injury or harm Also known as: Underdosing, as mode of injury or harm | underdosing of substance leading to inadequate level or effect of medication or substance as mode of injury | inadequate or insufficient dosage of substance, as mode of injury | missed or omitted dose of substance as mode of injury | dose of substance administered or taken too late or too slowly as mode of injury [PL13.0] Overdose of substance, as mode of injury or harm Definition: Incorrect dose - too high Also known as: Overdose of substance, as mode of injury or harm | wrong dose of substance as mode of injury | wrong strength of substance as mode of injury | dose of substance administered or taken too early or too quickly as a mode of injury | extra dose of substance administered as mode of injury Includes: overdose of prescribed drug | medication error leading to excess level or effect of prescribed drug Excludes: Overdose of substance without injury or harm | Unintentional exposure to or harmful effects of drugs, medicaments or biological substances | Intentional self-harm by exposure to or harmful effects of drugs, medicaments or biological substances [4A01.03] Transient hypogammaglobulinaemia of infancy Also known as: Transient hypogammaglobulinaemia of infancy | immunoglobulin maturational delay | THI - [transient hypogammaglobulinaemia of infancy] [2F21.Y] Other specified benign keratinocytic acanthomas Also known as: Other specified benign keratinocytic acanthomas | Stucco keratosis | Inverted follicular keratosis | Warty dyskeratoma | Clear cell acanthoma [2C73.00] Clear cell adenocarcinoma of ovary Definition: A malignant glandular epithelial tumour characterised by the presence of clear and hobnail cells. The tumour is highly associated with ovarian endometriosis, pelvic endometriosis and paraendocrine hypercalcemia. Also known as: Clear cell adenocarcinoma of ovary | clear cell carcinoma of ovary [2D12.1] Adenocarcinoma of other endocrine glands or related structures Also known as: Adenocarcinoma of other endocrine glands or related structures | Adenocarcinoma of parathyroid gland | water clear cell adenocarcinoma of unspecified site | water clear cell carcinoma of unspecified site | Adenocarcinoma of pituitary gland [2C25.Y] Other specified malignant neoplasms of bronchus or lung Also known as: Other specified malignant neoplasms of bronchus or lung | Bronchial endocrine tumour | Bronchial neuroendocrine tumour | Bronchial carcinoid tumour | Bronchiolo-alveolar carcinoma of lung [2C25.2] Squamous cell carcinoma of bronchus or lung Definition: A carcinoma arising from malignant squamous bronchial epithelial cells and characterised by the presence of keratinization and/or intercellular bridges. Cigarette smoking and arsenic exposure are strongly associated with squamous cell lung carcinoma. Also known as: Squamous cell carcinoma of bronchus or lung | Papillary squamous cell carcinoma of lung | Basaloid squamous cell carcinoma of lung | Clear cell squamous cell carcinoma of lung | Squamous cell cancer of lung === GRAPH WALKS === --- Walk 1 --- [NE60] Harmful effects of drugs, medicaments or biological substances, not elsewhere classified --PARENT--> [?] Harmful effects of substances --PARENT--> [22] Injury, poisoning or certain other consequences of external causes Def: !markdown In the ICD, injury means physical or physiological bodily harm resulting from interaction of the body with energy (mechanical, thermal, electrical, chemical or radiant, or due to extreme pre... --- Walk 2 --- [NE60] Harmful effects of drugs, medicaments or biological substances, not elsewhere classified --EXCLUDES--> [?] Disorders due to substance use or addictive behaviours Def: Disorders due to substance use and addictive behaviours are mental and behavioural disorders that develop as a result of the use of predominantly psychoactive substances, including medications, or spe... --CHILD--> [?] Disorders due to addictive behaviours Def: Disorders due to addictive behaviours are recognizable and clinically significant syndromes associated with distress or interference with personal functions that develop as a result of repetitive rewa... --- Walk 3 --- [PL00] Drugs, medicaments or biological substances associated with injury or harm in therapeutic use --EXCLUDES--> [?] Circumstances associated with exposure to a drug, medicament or biological substance influencing the episode of care without injury or harm --EXCLUDES--> [?] Mode of injury or harm associated with exposure to a drug, medicament or biological substance --- Walk 4 --- [PL00] Drugs, medicaments or biological substances associated with injury or harm in therapeutic use --EXCLUDES--> [?] Circumstances associated with exposure to a drug, medicament or biological substance influencing the episode of care without injury or harm --PARENT--> [?] Health care related circumstances influencing the episode of care without injury or harm --- Walk 5 --- [PL13.1] Underdosing, as mode of injury or harm --PARENT--> [PL13] Mode of injury or harm associated with exposure to a drug, medicament or biological substance --CHILD--> [PL13.2] Drug-related injury or harm in the context of correct administration or dosage, as mode of injury or harm --- Walk 6 --- [PL13.1] Underdosing, as mode of injury or harm --PARENT--> [PL13] Mode of injury or harm associated with exposure to a drug, medicament or biological substance --CHILD--> [PL13.2] Drug-related injury or harm in the context of correct administration or dosage, as mode of injury or harm
[ "[NE60] Harmful effects of drugs, medicaments or biological substances, not elsewhere classified\n --PARENT--> [?] Harmful effects of substances\n --PARENT--> [22] Injury, poisoning or certain other consequences of external causes\n Def: !markdown\nIn the ICD, injury means physical or physiological bodily harm resulting from interaction of the body with energy (mechanical, thermal, electrical, chemical or radiant, or due to extreme pre...", "[NE60] Harmful effects of drugs, medicaments or biological substances, not elsewhere classified\n --EXCLUDES--> [?] Disorders due to substance use or addictive behaviours\n Def: Disorders due to substance use and addictive behaviours are mental and behavioural disorders that develop as a result of the use of predominantly psychoactive substances, including medications, or spe...\n --CHILD--> [?] Disorders due to addictive behaviours\n Def: Disorders due to addictive behaviours are recognizable and clinically significant syndromes associated with distress or interference with personal functions that develop as a result of repetitive rewa...", "[PL00] Drugs, medicaments or biological substances associated with injury or harm in therapeutic use\n --EXCLUDES--> [?] Circumstances associated with exposure to a drug, medicament or biological substance influencing the episode of care without injury or harm\n --EXCLUDES--> [?] Mode of injury or harm associated with exposure to a drug, medicament or biological substance", "[PL00] Drugs, medicaments or biological substances associated with injury or harm in therapeutic use\n --EXCLUDES--> [?] Circumstances associated with exposure to a drug, medicament or biological substance influencing the episode of care without injury or harm\n --PARENT--> [?] Health care related circumstances influencing the episode of care without injury or harm", "[PL13.1] Underdosing, as mode of injury or harm\n --PARENT--> [PL13] Mode of injury or harm associated with exposure to a drug, medicament or biological substance\n --CHILD--> [PL13.2] Drug-related injury or harm in the context of correct administration or dosage, as mode of injury or harm", "[PL13.1] Underdosing, as mode of injury or harm\n --PARENT--> [PL13] Mode of injury or harm associated with exposure to a drug, medicament or biological substance\n --CHILD--> [PL13.2] Drug-related injury or harm in the context of correct administration or dosage, as mode of injury or harm" ]
NE60
Harmful effects of drugs, medicaments or biological substances, not elsewhere classified
[ { "from_icd11": "NE60", "icd10_code": "T50A95A", "icd10_title": "Adverse effect of other bacterial vaccines, initial encounter" }, { "from_icd11": "NE60", "icd10_code": "T50Z15A", "icd10_title": "Adverse effect of immunoglobulin, initial encounter" }, { "from_icd11": "NE60", "icd10_code": "T50Z95A", "icd10_title": "Adverse effect of other vaccines and biological substances, initial encounter" }, { "from_icd11": "NE60", "icd10_code": "T50A95S", "icd10_title": "Adverse effect of other bacterial vaccines, sequela" }, { "from_icd11": "NE60", "icd10_code": "T50B95A", "icd10_title": "Adverse effect of other viral vaccines, initial encounter" }, { "from_icd11": "NE60", "icd10_code": "T50A25A", "icd10_title": "Adverse effect of mixed bacterial vaccines without a pertussis component, initial encounter" }, { "from_icd11": "NE60", "icd10_code": "T50A91A", "icd10_title": "Poisoning by other bacterial vaccines, accidental (unintentional), initial encounter" }, { "from_icd11": "NE60", "icd10_code": "T498X5A", "icd10_title": "Adverse effect of other topical agents, initial encounter" }, { "from_icd11": "NE60", "icd10_code": "T48905A", "icd10_title": "Adverse effect of unspecified agents primarily acting on the respiratory system, initial encounter" }, { "from_icd11": "NE60", "icd10_code": "T48995A", "icd10_title": "Adverse effect of other agents primarily acting on the respiratory system, initial encounter" }, { "from_icd11": "NE60", "icd10_code": "T50A15A", "icd10_title": "Adverse effect of pertussis vaccine, including combinations with a pertussis component, initial encounter" }, { "from_icd11": "NE60", "icd10_code": "T50B15A", "icd10_title": "Adverse effect of smallpox vaccines, initial encounter" }, { "from_icd11": "NE60", "icd10_code": "T416X3A", "icd10_title": "" }, { "from_icd11": "NE60", "icd10_code": "T419X3A", "icd10_title": "" }, { "from_icd11": "NE60", "icd10_code": "T418X2A", "icd10_title": "" } ]
T50A95A
Adverse effect of other bacterial vaccines, initial encounter
The tip of the catheter that was left in the right posterior sectoral duct was not placed in the extrahepatic space of the cut liver surface but rather was pulled into the liver, so we anticipated that this bile duct would have fibrosed in the several month period of time between operations. This would make it nearly impossible to find at reoperation. To facilitate identifying this catheter in the operating room, we first had the catheter injected with contrast in the interventional radiology department on the morning of surgery in an attempt to advance the catheter into the extrahepatic space. This no longer revealed an extravasation of contrast as when the catheter was initially placed, thus indicating there was no communication of the catheter with the peritoneal cavity. Next, the patient was moved to the operating room, where we performed an exploratory laparotomy; however, the sheath containing the posterior sectoral catheter was left in place to allow further manipulation in the operating room. At operation, we appreciated a large amount of fibrosis around the liver in the area of her previous biliary abscess. Next, the anterior biliary duct endostent was identified by palpation. Dissection around the anterior biliary duct led to the finding of a disruption of this duct at the confluence. This represented site of the leak of the left hepatic ductal stump was initially detected in Figure 4 .
3.931641
0.953613
sec[1]/sec[0]/p[0]
en
0.999997
24159406
https://doi.org/10.1155/2013/202315
[ "catheter", "this", "duct", "liver", "operating", "room", "biliary", "that", "sectoral", "extrahepatic" ]
[ { "code": "QB62.Z", "title": "Attention to artificial openings, unspecified" }, { "code": "QB30.5", "title": "Fitting or adjustment of urinary device" }, { "code": "PK93.10", "title": "Gastroenterology or urology devices associated with injury or harm, urinary catheter" }, { "code": "PK90.1", "title": "Anaesthesiology devices associated with injury or harm, therapeutic, nonsurgical or rehabilitative devices" }, { "code": "PK91.2Y", "title": "Other specified cardiovascular devices associated with injury or harm, prosthetic or other implants, materials or accessory devices" }, { "code": "4A01.03", "title": "Transient hypogammaglobulinaemia of infancy" }, { "code": "DC10.02", "title": "Obstruction of bile duct" }, { "code": "DC10.00", "title": "Obstruction of cystic duct" }, { "code": "DC13", "title": "Cholangitis" }, { "code": "LB20.23", "title": "Structural developmental anomalies of cystic duct" } ]
=== ICD-11 CODES FOUND === [QB62.Z] Attention to artificial openings, unspecified Also known as: Attention to artificial openings, unspecified | Attention to artificial openings | toilet or cleansing of artificial opening | removal of catheter | passage of sounds or bougies [QB30.5] Fitting or adjustment of urinary device Also known as: Fitting or adjustment of urinary device | change of indwelling catheter | Removal of indwelling urinary catheter | removal of urinary catheter | removal of indwelling catheter [PK93.10] Gastroenterology or urology devices associated with injury or harm, urinary catheter Also known as: Gastroenterology or urology devices associated with injury or harm, urinary catheter | Gastroenterology or urology devices associated with adverse incidents, Foley catheter | Gastroenterology or urology devices associated with adverse incidents, indwelling urinary catheter | Mechanical complication of urinary catheter | Mechanical complication of urinary indwelling catheter Excludes: Circumstances associated with a surgical or other medical device influencing the episode of care without injury or harm [PK90.1] Anaesthesiology devices associated with injury or harm, therapeutic, nonsurgical or rehabilitative devices Definition: An anaesthesiology device was involved in an adverse incident that occurred in a therapeutic (nonsurgical) and rehabilitative task Also known as: Anaesthesiology devices associated with injury or harm, therapeutic, nonsurgical or rehabilitative devices | Anaesthesiology devices associated with injury or harm, spinal catheter | Mechanical complication of spinal catheter | Anaesthesiology devices associated with injury or harm, epidural catheter | Anaesthesiology devices associated with injury or harm, endotracheal tube Excludes: Circumstances associated with a surgical or other medical device influencing the episode of care without injury or harm [PK91.2Y] Other specified cardiovascular devices associated with injury or harm, prosthetic or other implants, materials or accessory devices Also known as: Other specified cardiovascular devices associated with injury or harm, prosthetic or other implants, materials or accessory devices | Cardiovascular devices associated with injury or harm, conduits | Mechanical complication of other cardiac and vascular devices and implants | Mechanical complication of artificial heart | Mechanical complication of vascular balloon implant or device [4A01.03] Transient hypogammaglobulinaemia of infancy Also known as: Transient hypogammaglobulinaemia of infancy | immunoglobulin maturational delay | THI - [transient hypogammaglobulinaemia of infancy] [DC10.02] Obstruction of bile duct Also known as: Obstruction of bile duct | extrahepatic biliary obstruction | extrahepatic bile duct obstruction | bile duct obstruction | bile stasis Excludes: with cholelithiasis [DC10.00] Obstruction of cystic duct Also known as: Obstruction of cystic duct | cystic duct obstruction | cystic ductal obstruction | obstructed cystic duct | Acquired cystic duct atresia [DC13] Cholangitis Also known as: Cholangitis | acute cholangiolitis | ascending cholangitis | cholangiolitis | cholangitis NOS Excludes: chronic nonsuppurative destructive cholangitis | cholangitis with cholelithiasis | Primary sclerosing cholangitis [LB20.23] Structural developmental anomalies of cystic duct Also known as: Structural developmental anomalies of cystic duct | congenital deformity of cystic duct | cystic duct anomaly | cystic duct deformity | cystic duct distortion === GRAPH WALKS === --- Walk 1 --- [QB62.Z] Attention to artificial openings, unspecified --PARENT--> [QB62] Attention to artificial openings --EXCLUDES--> [?] Tracheostomy malfunction --- Walk 2 --- [QB62.Z] Attention to artificial openings, unspecified --PARENT--> [QB62] Attention to artificial openings --CHILD--> [QB62.1] Attention to gastrostomy --- Walk 3 --- [QB30.5] Fitting or adjustment of urinary device --PARENT--> [QB30] Adjustment or management of implanted devices --CHILD--> [QB30.0] Adjustment or management of implanted hearing device --- Walk 4 --- [QB30.5] Fitting or adjustment of urinary device --PARENT--> [QB30] Adjustment or management of implanted devices --CHILD--> [QB30.0] Adjustment or management of implanted hearing device --- Walk 5 --- [PK93.10] Gastroenterology or urology devices associated with injury or harm, urinary catheter --PARENT--> [PK93.1] Gastroenterology or urology devices associated with injury or harm, therapeutic, nonsurgical or rehabilitative devices Def: A gastroenterology or urology device was involved in an adverse incident that occurred in a therapeutic (nonsurgical) and rehabilitative task... --EXCLUDES--> [?] Circumstances associated with a surgical or other medical device influencing the episode of care without injury or harm --- Walk 6 --- [PK93.10] Gastroenterology or urology devices associated with injury or harm, urinary catheter --EXCLUDES--> [?] Circumstances associated with a surgical or other medical device influencing the episode of care without injury or harm --EXCLUDES--> [?] Mode of injury or harm associated with a surgical or other medical device, implant or graft
[ "[QB62.Z] Attention to artificial openings, unspecified\n --PARENT--> [QB62] Attention to artificial openings\n --EXCLUDES--> [?] Tracheostomy malfunction", "[QB62.Z] Attention to artificial openings, unspecified\n --PARENT--> [QB62] Attention to artificial openings\n --CHILD--> [QB62.1] Attention to gastrostomy", "[QB30.5] Fitting or adjustment of urinary device\n --PARENT--> [QB30] Adjustment or management of implanted devices\n --CHILD--> [QB30.0] Adjustment or management of implanted hearing device", "[QB30.5] Fitting or adjustment of urinary device\n --PARENT--> [QB30] Adjustment or management of implanted devices\n --CHILD--> [QB30.0] Adjustment or management of implanted hearing device", "[PK93.10] Gastroenterology or urology devices associated with injury or harm, urinary catheter\n --PARENT--> [PK93.1] Gastroenterology or urology devices associated with injury or harm, therapeutic, nonsurgical or rehabilitative devices\n Def: A gastroenterology or urology device was involved in an adverse incident that occurred in a therapeutic (nonsurgical) and rehabilitative task...\n --EXCLUDES--> [?] Circumstances associated with a surgical or other medical device influencing the episode of care without injury or harm", "[PK93.10] Gastroenterology or urology devices associated with injury or harm, urinary catheter\n --EXCLUDES--> [?] Circumstances associated with a surgical or other medical device influencing the episode of care without injury or harm\n --EXCLUDES--> [?] Mode of injury or harm associated with a surgical or other medical device, implant or graft" ]
QB62.Z
Attention to artificial openings, unspecified
[ { "from_icd11": "QB62.Z", "icd10_code": "Z436", "icd10_title": "Encounter for attention to other artificial openings of urinary tract" }, { "from_icd11": "QB62.Z", "icd10_code": "Z434", "icd10_title": "Encounter for attention to other artificial openings of digestive tract" }, { "from_icd11": "QB62.Z", "icd10_code": "Z438", "icd10_title": "Encounter for attention to other artificial openings" }, { "from_icd11": "QB62.Z", "icd10_code": "Z439", "icd10_title": "Encounter for attention to unspecified artificial opening" }, { "from_icd11": "QB62.Z", "icd10_code": "Z43", "icd10_title": "Encounter for attention to artificial openings" }, { "from_icd11": "QB30.5", "icd10_code": "Z466", "icd10_title": "Encounter for fitting and adjustment of urinary device" }, { "from_icd11": "PK93.10", "icd10_code": "T83022A", "icd10_title": "Displacement of nephrostomy catheter, initial encounter" }, { "from_icd11": "PK93.10", "icd10_code": "T83020A", "icd10_title": "Displacement of cystostomy catheter, initial encounter" }, { "from_icd11": "PK93.10", "icd10_code": "T83032A", "icd10_title": "Leakage of nephrostomy catheter, initial encounter" }, { "from_icd11": "PK93.10", "icd10_code": "T83092A", "icd10_title": "Other mechanical complication of nephrostomy catheter, initial encounter" }, { "from_icd11": "PK93.10", "icd10_code": "T83021A", "icd10_title": "Displacement of indwelling urethral catheter, initial encounter" }, { "from_icd11": "PK93.10", "icd10_code": "T83028A", "icd10_title": "Displacement of other urinary catheter, initial encounter" }, { "from_icd11": "PK93.10", "icd10_code": "T83090A", "icd10_title": "Other mechanical complication of cystostomy catheter, initial encounter" }, { "from_icd11": "PK93.10", "icd10_code": "T83012A", "icd10_title": "Breakdown (mechanical) of nephrostomy catheter, initial encounter" }, { "from_icd11": "PK93.10", "icd10_code": "T83030A", "icd10_title": "Leakage of cystostomy catheter, initial encounter" } ]
Z436
Encounter for attention to other artificial openings of urinary tract
Thirteen months later, nephrotic syndrome (proteinuria of 6.3 g/day) occurred after a respiratory infection. Estimated glomerular filtration rate (eGFR) was 108.6 mL/minute per 1.73 m 2 . Both leukocyturia and microscopic hematuria deteriorated. Anti-nuclear antibody titer was 1:160, and leukocytosis (13,300 cells per microliter) persisted. Complement C3 and C4 were within normal range, and cryoglobulinemia was ruled out. Both plasma and urinary protein immunofixations were unremarkable. Abdominal ultrasound, gynecologic, pulmologic, and urologic exams yielded normal results. Cardiac workup, including echocardiography and electrocardiography (ECG), was unrevealing except for an incomplete right bundle branch block and intraventricular conductance abnormalities in ECG leads II and aVF. A second renal biopsy confirmed FibGN. The prednisolone dose was temporarily increased (60 mg/day for three months and tapered off to 5 mg every other day) and had to be discontinued after five more months because of side effects consistent with iatrogenic Cushing's syndrome (for example, weight gain, glucose intolerance, mood changes, and typical fat distribution). After discontinuation of steroids, proteinuria remained below 3 g/day for three years. However, over the course of a total of five years without immunosuppressive therapy, proteinuria worsened (4.8 g/day) and eGFR decreased to 64 mL/minute per 1.73 m 2 .
4.125
0.964844
sec[1]/p[2]
en
0.999996
22531147
https://doi.org/10.1186/1752-1947-6-116
[ "proteinuria", "egfr", "minute", "both", "three", "five", "thirteen", "nephrotic", "occurred", "respiratory" ]
[ { "code": "MF96.Z", "title": "Proteinuria, unspecified" }, { "code": "MF96.Y", "title": "Other specified proteinuria" }, { "code": "GB4Y", "title": "Other specified glomerular diseases" }, { "code": "MF96.0", "title": "Orthostatic proteinuria" }, { "code": "JA22.0", "title": "Gestational proteinuria without hypertension" }, { "code": "GB61.1", "title": "Chronic kidney disease, stage 2" }, { "code": "GB61.5", "title": "Chronic kidney disease, stage 5" }, { "code": "GB61.4", "title": "Chronic kidney disease, stage 4" }, { "code": "GB61.3", "title": "Chronic kidney disease, stage 3b" }, { "code": "GB61.0", "title": "Chronic kidney disease, stage 1" } ]
=== ICD-11 CODES FOUND === [MF96.Z] Proteinuria, unspecified Also known as: Proteinuria, unspecified | Proteinuria | Albuminuria NOS | Proteinuria NOS [MF96.Y] Other specified proteinuria Also known as: Other specified proteinuria [GB4Y] Other specified glomerular diseases Also known as: Other specified glomerular diseases | Glomerular disease classified by clinical features or syndromes | Chronic proteinuria | Permanent proteinuria with focal and segmental hyalinosis without nephrotic syndrome | Recurrent or persistent glomerular haematuria [MF96.0] Orthostatic proteinuria Definition: A condition characterised by an elevated protein excretion while in the upright position and normal protein excretion in a supine or recumbent position. Also known as: Orthostatic proteinuria | benign postural proteinuria | orthostatic albuminuria | postural albuminuria | postural proteinuria [JA22.0] Gestational proteinuria without hypertension Also known as: Gestational proteinuria without hypertension | proteinuria complicating pregnancy | puerperal albuminuria | Gestational proteinuria, intermittent | Gestational proteinuria, persistent [GB61.1] Chronic kidney disease, stage 2 Definition: Kidney damage and GFR 60-89 ml/min/1.73m² Also known as: Chronic kidney disease, stage 2 | kidney damage and mild decrease in GFR | chronic renal failure, stage 2 | CKD - [chronic kidney disease] stage 2 | kidney damage and mild decrease in eGFR - [estimated glomerular filtration rate] Includes: chronic renal failure, stage 2 [GB61.5] Chronic kidney disease, stage 5 Definition: Kidney failure, GFR < 15 ml/min/1.73m² Also known as: Chronic kidney disease, stage 5 | chronic renal failure, stage 5 | CKD - [chronic kidney disease] stage 5 | end stage kidney failure | end stage renal failure Includes: chronic renal failure, stage 5 [GB61.4] Chronic kidney disease, stage 4 Definition: GFR (15-29 ml/min/1.73m²) Also known as: Chronic kidney disease, stage 4 | severe decrease in GFR | chronic renal failure, stage 4 | CKD - [chronic kidney disease] stage 4 | eGFR - [estimated glomerular filtration rate] 15-29 ml/min/1.73m² Includes: chronic renal failure, stage 4 [GB61.3] Chronic kidney disease, stage 3b Definition: GFR 30-44 ml/min/1.73m² Also known as: Chronic kidney disease, stage 3b | chronic renal failure, stage 3b | CKD - [chronic kidney disease] stage 3b | eGFR - [estimated glomerular filtration rate] 30-44 ml/min/1.73m² Includes: chronic renal failure, stage 3b [GB61.0] Chronic kidney disease, stage 1 Definition: Kidney damage with normal or increased GFR (>90 ml/min/1.73m²) Also known as: Chronic kidney disease, stage 1 | chronic renal failure, stage 1 | CKD - [chronic kidney disease] stage 1 | normal or increased eGFR (>90 ml/min/1.73m²) Includes: chronic renal failure, stage 1 === GRAPH WALKS === --- Walk 1 --- [MF96.Z] Proteinuria, unspecified --PARENT--> [MF96] Proteinuria Def: Excessive serum proteins in the urine, such as in renal disease when albumin is the main protein, but also may be due to other proteins such as immunoglobulin light chains in plasma cell dyscrasia suc... --RELATED_TO--> [?] Gestational oedema with proteinuria without hypertension Def: The accumulation of fluid and proteinuria due to the physiological alterations of pregnancy in the absence of hypertension... --- Walk 2 --- [MF96.Z] Proteinuria, unspecified --PARENT--> [MF96] Proteinuria Def: Excessive serum proteins in the urine, such as in renal disease when albumin is the main protein, but also may be due to other proteins such as immunoglobulin light chains in plasma cell dyscrasia suc... --RELATED_TO--> [?] Gestational oedema with proteinuria without hypertension Def: The accumulation of fluid and proteinuria due to the physiological alterations of pregnancy in the absence of hypertension... --- Walk 3 --- [MF96.Y] Other specified proteinuria --PARENT--> [MF96] Proteinuria Def: Excessive serum proteins in the urine, such as in renal disease when albumin is the main protein, but also may be due to other proteins such as immunoglobulin light chains in plasma cell dyscrasia suc... --EXCLUDES--> [?] Persistent proteinuria or albuminuria Def: Persistent albuminuria >3mg/mmol creatinine or >30mg/day is regarded as abnormal, indicative and often the first manifestation of chronic kidney disease (CKD). In surveillance for CKD in “at risk” pat... --- Walk 4 --- [MF96.Y] Other specified proteinuria --PARENT--> [MF96] Proteinuria Def: Excessive serum proteins in the urine, such as in renal disease when albumin is the main protein, but also may be due to other proteins such as immunoglobulin light chains in plasma cell dyscrasia suc... --CHILD--> [MF96.0] Orthostatic proteinuria Def: A condition characterised by an elevated protein excretion while in the upright position and normal protein excretion in a supine or recumbent position.... --- Walk 5 --- [GB4Y] Other specified glomerular diseases --PARENT--> [?] Glomerular diseases Def: Any disease characterised by pathological changes to the glomerulus.... --CHILD--> [GB41] Nephrotic syndrome Def: A condition characterised by severe proteinuria, greater than 3.5 g/day in an average adult. The substantial loss of protein in the urine results in hypoalbuminaemia and generalised oedema. There is a... --- Walk 6 --- [GB4Y] Other specified glomerular diseases --PARENT--> [?] Glomerular diseases Def: Any disease characterised by pathological changes to the glomerulus.... --RELATED_TO--> [?] Plasmodium malariae malaria with nephropathy Def: Quartan malarial nephropathy is a rare complication of malariae (quartan) malaria, especially occurring in children; it is a glomerulonephritis, usually fatal....
[ "[MF96.Z] Proteinuria, unspecified\n --PARENT--> [MF96] Proteinuria\n Def: Excessive serum proteins in the urine, such as in renal disease when albumin is the main protein, but also may be due to other proteins such as immunoglobulin light chains in plasma cell dyscrasia suc...\n --RELATED_TO--> [?] Gestational oedema with proteinuria without hypertension\n Def: The accumulation of fluid and proteinuria due to the physiological alterations of pregnancy in the absence of hypertension...", "[MF96.Z] Proteinuria, unspecified\n --PARENT--> [MF96] Proteinuria\n Def: Excessive serum proteins in the urine, such as in renal disease when albumin is the main protein, but also may be due to other proteins such as immunoglobulin light chains in plasma cell dyscrasia suc...\n --RELATED_TO--> [?] Gestational oedema with proteinuria without hypertension\n Def: The accumulation of fluid and proteinuria due to the physiological alterations of pregnancy in the absence of hypertension...", "[MF96.Y] Other specified proteinuria\n --PARENT--> [MF96] Proteinuria\n Def: Excessive serum proteins in the urine, such as in renal disease when albumin is the main protein, but also may be due to other proteins such as immunoglobulin light chains in plasma cell dyscrasia suc...\n --EXCLUDES--> [?] Persistent proteinuria or albuminuria\n Def: Persistent albuminuria >3mg/mmol creatinine or >30mg/day is regarded as abnormal, indicative and often the first manifestation of chronic kidney disease (CKD). In surveillance for CKD in “at risk” pat...", "[MF96.Y] Other specified proteinuria\n --PARENT--> [MF96] Proteinuria\n Def: Excessive serum proteins in the urine, such as in renal disease when albumin is the main protein, but also may be due to other proteins such as immunoglobulin light chains in plasma cell dyscrasia suc...\n --CHILD--> [MF96.0] Orthostatic proteinuria\n Def: A condition characterised by an elevated protein excretion while in the upright position and normal protein excretion in a supine or recumbent position....", "[GB4Y] Other specified glomerular diseases\n --PARENT--> [?] Glomerular diseases\n Def: Any disease characterised by pathological changes to the glomerulus....\n --CHILD--> [GB41] Nephrotic syndrome\n Def: A condition characterised by severe proteinuria, greater than 3.5 g/day in an average adult. The substantial loss of protein in the urine results in hypoalbuminaemia and generalised oedema. There is a...", "[GB4Y] Other specified glomerular diseases\n --PARENT--> [?] Glomerular diseases\n Def: Any disease characterised by pathological changes to the glomerulus....\n --RELATED_TO--> [?] Plasmodium malariae malaria with nephropathy\n Def: Quartan malarial nephropathy is a rare complication of malariae (quartan) malaria, especially occurring in children; it is a glomerulonephritis, usually fatal...." ]
MF96.Z
Proteinuria, unspecified
[ { "from_icd11": "MF96.Z", "icd10_code": "R809", "icd10_title": "Proteinuria, unspecified" }, { "from_icd11": "MF96.Z", "icd10_code": "R803", "icd10_title": "Bence Jones proteinuria" }, { "from_icd11": "MF96.Z", "icd10_code": "R808", "icd10_title": "Other proteinuria" }, { "from_icd11": "MF96.Z", "icd10_code": "R801", "icd10_title": "Persistent proteinuria, unspecified" }, { "from_icd11": "MF96.Z", "icd10_code": "N391", "icd10_title": "" }, { "from_icd11": "MF96.Z", "icd10_code": "R80", "icd10_title": "Proteinuria" }, { "from_icd11": "MF96.0", "icd10_code": "N2889", "icd10_title": "Other specified disorders of kidney and ureter" }, { "from_icd11": "MF96.0", "icd10_code": "N2882", "icd10_title": "Megaloureter" }, { "from_icd11": "MF96.0", "icd10_code": "N2886", "icd10_title": "Ureteritis cystica" }, { "from_icd11": "MF96.0", "icd10_code": "N2881", "icd10_title": "Hypertrophy of kidney" }, { "from_icd11": "MF96.0", "icd10_code": "N2884", "icd10_title": "Pyelitis cystica" }, { "from_icd11": "MF96.0", "icd10_code": "N2885", "icd10_title": "Pyeloureteritis cystica" }, { "from_icd11": "MF96.0", "icd10_code": "N288", "icd10_title": "Other specified disorders of kidney and ureter" }, { "from_icd11": "MF96.0", "icd10_code": "N392", "icd10_title": "" }, { "from_icd11": "JA22.0", "icd10_code": "O1213", "icd10_title": "Gestational proteinuria, third trimester" } ]
R809
Proteinuria, unspecified
This case illustrates the unusual case of a supraventricular tachycardia degenerating to VT in a patient with ischemic heart disease. Tachycardia-induced tachycardia is a rare condition. Cases have been described of AVNRT coincident with right ventricular outflow tract tachycardia or with left ventricular tachycardia . In some cases where AVNRT spontaneously triggered VT, catheter ablation of the slow pathway did not suppress subsequent inducibility of VT and ablation of both substrates of arrhythmia is recommended . Monomorphic VT is a frequent finding in patients with an old myocardial infarction, in which the scar represents the pathological substrate responsible for the re-entrant circuit. Polymorphic VT is a less frequent event in patients with chronic ischemic heart disease, both as a primary arrhythmia and as a finding during programmed ventricular stimulation, specially in patients after an episode of aborted sudden death . Polymorphic VT is more related to additional factors like electrolyte imbalance, ischemia, long QT, Brugada syndrome, catecholaminergic polymorphic VT, but all these factors were excluded in our case . The presence of ischemic heart disease with an old myocardial infarction without evidence of an acute ischemic milieu, recovered sudden death and inducibility of non-sustained polymorphic VT after successful slow pathway ablation lead us to implant an ICD to our patient.
4.15625
0.954102
sec[1]/p[0]
en
0.999998
21197279
N/A
[ "tachycardia", "ischemic", "polymorphic", "heart", "ventricular", "ablation", "patients", "cases", "avnrt", "slow" ]
[ { "code": "MC81.0", "title": "Tachycardia, unspecified" }, { "code": "BC71.0Z", "title": "Ventricular tachycardia, unspecified" }, { "code": "MC81.3", "title": "Paroxysmal tachycardia" }, { "code": "BC71.0Y", "title": "Other specified ventricular tachycardia" }, { "code": "BC81.0", "title": "Ectopic atrial tachycardia" }, { "code": "DD3Z", "title": "Ischaemic vascular disorders of intestine, unspecified" }, { "code": "BA5Z", "title": "Chronic ischaemic heart disease, unspecified" }, { "code": "BA4Z", "title": "Acute ischaemic heart disease, unspecified" }, { "code": "GB90.3", "title": "Ischaemia or infarction of kidney" }, { "code": "8B1Z", "title": "Cerebral ischaemia, unspecified" } ]
=== ICD-11 CODES FOUND === [MC81.0] Tachycardia, unspecified Also known as: Tachycardia, unspecified | heart rate fast | rapid heart | Rapid heart beat | increased heart rate [BC71.0Z] Ventricular tachycardia, unspecified Also known as: Ventricular tachycardia, unspecified | Ventricular tachycardia | VT - [ventricular tachycardia] | ventricular tachycardia NOS | paroxysmal ventricular tachycardia [MC81.3] Paroxysmal tachycardia Also known as: Paroxysmal tachycardia | Bouveret-Hoffmann syndrome | Bouveret syndrome | essential paroxysmal tachycardia | paroxysmal tachycardia NOS Excludes: complicating, abortion or ectopic or molar pregnancy [BC71.0Y] Other specified ventricular tachycardia Also known as: Other specified ventricular tachycardia | Monomorphic ventricular tachycardia | Secondary monomorphic ventricular tachycardia associated with diseases classified elsewhere | Left outflow tract ventricular tachycardia | Idiopathic fascicular ventricular tachycardia [BC81.0] Ectopic atrial tachycardia Definition: Ectopic atrial tachycardia originates from a small area (focus) in the atrium and spreading centrifugally. Also known as: Ectopic atrial tachycardia | Focal atrial tachycardia | Ectopic atrial tachycardia, automatic | focal atrial tachycardia, automatic | Ectopic atrial tachycardia, nonautomatic [DD3Z] Ischaemic vascular disorders of intestine, unspecified Also known as: Ischaemic vascular disorders of intestine, unspecified | Vascular disorder of intestine, not elsewhere classified | vascular disorder of intestine | vascular bowel disease | ischaemic gut NOS [BA5Z] Chronic ischaemic heart disease, unspecified Also known as: Chronic ischaemic heart disease, unspecified | Ischaemic heart disease (chronic) NOS | coronary ischaemia | coronary damage NOS | atheroma of heart [BA4Z] Acute ischaemic heart disease, unspecified Also known as: Acute ischaemic heart disease, unspecified | acute coronary syndrome | ACS - [acute coronary syndrome] | Silent myocardial ischaemia | asymptomatic ischemia [GB90.3] Ischaemia or infarction of kidney Also known as: Ischaemia or infarction of kidney | Complete arterial ischaemia or infarction of kidney | Complete arterial ischaemia or infarction of kidney due to renal artery obstruction | obstructed renal artery | renal artery clot Excludes: Atherosclerosis of renal artery | Goldblatt kidney | Congenital renal artery stenosis [8B1Z] Cerebral ischaemia, unspecified Also known as: Cerebral ischaemia, unspecified | brain ischaemia | cerebrovascular ischaemic disease | cerebrovascular ischaemia | cerebral anaemia === GRAPH WALKS === --- Walk 1 --- [MC81.0] Tachycardia, unspecified --PARENT--> [MC81] Abnormalities of heart beat Def: Abnormalities of heart beat is arrhythmia which is any disorder of the heart rate or rhythm. It means that the heart beats too quickly, too slowly or with an irregular pattern.... --EXCLUDES--> [?] Cardiac arrhythmia Def: This is any of a large and heterogeneous group of conditions in which there is abnormal electrical activity in the heart. The heartbeat may be too fast or too slow, and may be regular or irregular.... --- Walk 2 --- [MC81.0] Tachycardia, unspecified --PARENT--> [MC81] Abnormalities of heart beat Def: Abnormalities of heart beat is arrhythmia which is any disorder of the heart rate or rhythm. It means that the heart beats too quickly, too slowly or with an irregular pattern.... --CHILD--> [MC81.2] Palpitations --- Walk 3 --- [BC71.0Z] Ventricular tachycardia, unspecified --PARENT--> [BC71.0] Ventricular tachycardia Def: Ventricular tachycardia is a cardiac arrhythmia of three or more consecutive complexes in duration emanating from the ventricles at a rate of greater than 120 bpm in adolescents or adults and a rate g... --CHILD--> [BC71.01] Polymorphic ventricular tachycardia Def: Ventricular tachycardia with 2 or more QRS morphologies.... --- Walk 4 --- [BC71.0Z] Ventricular tachycardia, unspecified --PARENT--> [BC71.0] Ventricular tachycardia Def: Ventricular tachycardia is a cardiac arrhythmia of three or more consecutive complexes in duration emanating from the ventricles at a rate of greater than 120 bpm in adolescents or adults and a rate g... --CHILD--> [BC71.02] Sustained ventricular tachycardia Def: Ventricular tachycardia that has a duration of >30 seconds or causes haemodynamic instability.... --- Walk 5 --- [MC81.3] Paroxysmal tachycardia --RELATED_TO--> [?] Re-entry ventricular arrhythmia --PARENT--> [?] Paroxysmal tachycardia --- Walk 6 --- [MC81.3] Paroxysmal tachycardia --RELATED_TO--> [?] Re-entry ventricular arrhythmia --PARENT--> [?] Ventricular tachyarrhythmia Def: Any ventricular rhythm disturbance with a rate faster than the normal age dependent ventricular escape rate....
[ "[MC81.0] Tachycardia, unspecified\n --PARENT--> [MC81] Abnormalities of heart beat\n Def: Abnormalities of heart beat is arrhythmia which is any disorder of the heart rate or rhythm. It means that the heart beats too quickly, too slowly or with an irregular pattern....\n --EXCLUDES--> [?] Cardiac arrhythmia\n Def: This is any of a large and heterogeneous group of conditions in which there is abnormal electrical activity in the heart. The heartbeat may be too fast or too slow, and may be regular or irregular....", "[MC81.0] Tachycardia, unspecified\n --PARENT--> [MC81] Abnormalities of heart beat\n Def: Abnormalities of heart beat is arrhythmia which is any disorder of the heart rate or rhythm. It means that the heart beats too quickly, too slowly or with an irregular pattern....\n --CHILD--> [MC81.2] Palpitations", "[BC71.0Z] Ventricular tachycardia, unspecified\n --PARENT--> [BC71.0] Ventricular tachycardia\n Def: Ventricular tachycardia is a cardiac arrhythmia of three or more consecutive complexes in duration emanating from the ventricles at a rate of greater than 120 bpm in adolescents or adults and a rate g...\n --CHILD--> [BC71.01] Polymorphic ventricular tachycardia\n Def: Ventricular tachycardia with 2 or more QRS morphologies....", "[BC71.0Z] Ventricular tachycardia, unspecified\n --PARENT--> [BC71.0] Ventricular tachycardia\n Def: Ventricular tachycardia is a cardiac arrhythmia of three or more consecutive complexes in duration emanating from the ventricles at a rate of greater than 120 bpm in adolescents or adults and a rate g...\n --CHILD--> [BC71.02] Sustained ventricular tachycardia\n Def: Ventricular tachycardia that has a duration of >30 seconds or causes haemodynamic instability....", "[MC81.3] Paroxysmal tachycardia\n --RELATED_TO--> [?] Re-entry ventricular arrhythmia\n --PARENT--> [?] Paroxysmal tachycardia", "[MC81.3] Paroxysmal tachycardia\n --RELATED_TO--> [?] Re-entry ventricular arrhythmia\n --PARENT--> [?] Ventricular tachyarrhythmia\n Def: Any ventricular rhythm disturbance with a rate faster than the normal age dependent ventricular escape rate...." ]
MC81.0
Tachycardia, unspecified
[ { "from_icd11": "MC81.0", "icd10_code": "R000", "icd10_title": "Tachycardia, unspecified" }, { "from_icd11": "BC71.0Z", "icd10_code": "I472", "icd10_title": "Ventricular tachycardia" }, { "from_icd11": "MC81.3", "icd10_code": "I479", "icd10_title": "Paroxysmal tachycardia, unspecified" }, { "from_icd11": "MC81.3", "icd10_code": "I47", "icd10_title": "Paroxysmal tachycardia" }, { "from_icd11": "BC81.0", "icd10_code": "I471", "icd10_title": "Supraventricular tachycardia" }, { "from_icd11": "DD3Z", "icd10_code": "K559", "icd10_title": "Vascular disorder of intestine, unspecified" }, { "from_icd11": "DD3Z", "icd10_code": "K558", "icd10_title": "Other vascular disorders of intestine" }, { "from_icd11": "DD3Z", "icd10_code": "K55-K64", "icd10_title": "" }, { "from_icd11": "DD3Z", "icd10_code": "K55", "icd10_title": "Vascular disorders of intestine" }, { "from_icd11": "BA5Z", "icd10_code": "I25709", "icd10_title": "Atherosclerosis of coronary artery bypass graft(s), unspecified, with unspecified angina pectoris" }, { "from_icd11": "BA5Z", "icd10_code": "I25718", "icd10_title": "Atherosclerosis of autologous vein coronary artery bypass graft(s) with other forms of angina pectoris" }, { "from_icd11": "BA5Z", "icd10_code": "I25710", "icd10_title": "Atherosclerosis of autologous vein coronary artery bypass graft(s) with unstable angina pectoris" }, { "from_icd11": "BA5Z", "icd10_code": "I25700", "icd10_title": "Atherosclerosis of coronary artery bypass graft(s), unspecified, with unstable angina pectoris" }, { "from_icd11": "BA5Z", "icd10_code": "I25719", "icd10_title": "Atherosclerosis of autologous vein coronary artery bypass graft(s) with unspecified angina pectoris" }, { "from_icd11": "BA5Z", "icd10_code": "I25720", "icd10_title": "Atherosclerosis of autologous artery coronary artery bypass graft(s) with unstable angina pectoris" } ]
R000
Tachycardia, unspecified
Cystic lymphangiomas as seen in case 2 are sometimes clinically difficult to differentiate from mesenteric and omental cysts . Cystic lymphangiomas have an endothelial cell lining, foam cells, and a thin wall that contains lymphatic spaces, lymphoid tissue, and smooth muscle. Mesenteric cysts lack smooth muscle and lymphatic spaces, and the cells lining the cysts are cuboidal or columnar in nature. An omental cyst has the same histological characteristics as a mesenteric cyst but is confined to the greater and lesser omentum. Lymphangiomas are more diffuse and occur in the mesentery or retroperitoneum, and patients may present with them earlier in life than those with mesenteric or omental cysts . Long-term follow-up with ultrasonography scan is important, especially where complete excision has not been achieved because of risk of recurrence . Even though the child with cystic lymphangioma (case 2) developed a recurrence, it is small and well localized compared to the initial presentation without any mass effect. Given that the child continues to remain asymptomatic and its extremely small size (<2 cm) we plan to follow up with this child with serial pelvic ultrasonography. If the child does develop symptoms related to mass effect of this recurrent cyst or there is an increase in size on serial ultrasound scans, we would elect to resect this cyst, using the same surgical technique described here.
4.1875
0.645996
sec[3]/p[6]
en
0.999996
26798349
https://doi.org/10.1155/2015/937191
[ "mesenteric", "cysts", "cyst", "cystic", "lymphangiomas", "omental", "this", "lining", "cells", "that" ]
[ { "code": "DC51.Y&XA43V8", "title": "Mesentery rupture" }, { "code": "LB18", "title": "Congenital anomalies of intestinal fixation" }, { "code": "DD31.0Z", "title": "Non-occlusive mesenteric ischaemia, unspecified" }, { "code": "DD30.0", "title": "Acute mesenteric arterial infarction" }, { "code": "DC51.1&XA43V8", "title": "Adhesion of mesentery" }, { "code": "FB80.5", "title": "Solitary bone cyst" }, { "code": "EK70.Z", "title": "Cutaneous cysts, unspecified" }, { "code": "FB4Y", "title": "Other specified disorders of synovium or tendon" }, { "code": "CA0C", "title": "Cyst or mucocele of nose or nasal sinus" }, { "code": "9A7Y", "title": "Other specified disorders of the cornea" } ]
=== ICD-11 CODES FOUND === [LB18] Congenital anomalies of intestinal fixation Definition: A condition caused by failure of the intestines to correctly develop during the antenatal period. This condition may present with intermittent abdominal pain, vomiting, or diarrhoea. Confirmation is through observation of intestinal rotation by imaging. Also known as: Congenital anomalies of intestinal fixation | Congenital malrotation of large intestine | Congenital intestinal malrotation | Volvulus of midgut | Volvulus neonatorum [DD31.0Z] Non-occlusive mesenteric ischaemia, unspecified Also known as: Non-occlusive mesenteric ischaemia, unspecified | Non-occlusive mesenteric ischaemia | NOMI - [non-occlusive mesenteric ischaemia] | mesenteric ischaemia [DD30.0] Acute mesenteric arterial infarction Definition: Acute mesenteric arterial infarction is an ischemic disorder of sudden interruption of mesenteric arterial flow because of occlusion of mesenteric artery. This may be further subdivided into acute mesenteric arterial embolus (AMAE) and acute mesenteric arterial thrombosis (AMAT). Also known as: Acute mesenteric arterial infarction | OMAI - [occlusive mesenteric arterial ischemia] | mesenteric arterial occlusion | mesenteric infarct | mesenteric infarction [FB80.5] Solitary bone cyst Definition: A solitary bone cyst is a benign non-epithelial bone cavity that is asymptomatic and that is found most commonly in the second decade of life by chance. The long bones are most often affected, but cases involving the jaw bone have been reported. Also known as: Solitary bone cyst | cyst of bone | local cyst of bone | simple bone cyst | solitary bone cyst, unspecified site Excludes: solitary cyst of jaw [EK70.Z] Cutaneous cysts, unspecified Also known as: Cutaneous cysts, unspecified | Cutaneous cysts | Follicular cysts of skin and subcutaneous tissue [FB4Y] Other specified disorders of synovium or tendon Also known as: Other specified disorders of synovium or tendon | Shortening of tendon | short tendon | Shortening of tibialis anterior | Contracture of tendon [CA0C] Cyst or mucocele of nose or nasal sinus Definition: A condition which refers to diseases of the nose and nasal sinus that cause a cyst or mucocele. A mucocele is any dilatation (typically pathologic) with accumulation of mucus. Mucoceles are benign, epithelium-lined cysts filled with mucus, which can form in the paranasal sinuses. These structures may cause symptoms if sufficiently large or if exerting pressure on surrounding anatomic structures. Symptomatic mucoceles typically require surgical intervention. Mucoceles should be differentiated fro Also known as: Cyst or mucocele of nose or nasal sinus | cyst of sinus | mucocele of sinus | Cyst of maxillary sinus | cyst of maxillary antrum [9A7Y] Other specified disorders of the cornea Also known as: Other specified disorders of the cornea | Secondary disorders of sclera or cornea | Disorders of sclera and cornea in diseases classified elsewhere | Secondary keratitis or keratoconjunctivitis | Keratitis and keratoconjunctivitis in other diseases classified elsewhere === GRAPH WALKS === --- Walk 1 --- [LB18] Congenital anomalies of intestinal fixation Def: A condition caused by failure of the intestines to correctly develop during the antenatal period. This condition may present with intermittent abdominal pain, vomiting, or diarrhoea. Confirmation is t... --PARENT--> [?] Structural developmental anomalies of the digestive tract Def: Any condition caused by failure of the digestive tract to correctly develop during the antenatal period.... --CHILD--> [LB11] Congenital diverticulum of pharynx Def: A condition caused by failure of the pharynx to correctly develop during the antenatal period. This condition may present with difficulty swallowing, or may be asymptomatic. Confirmation is through ob... --- Walk 2 --- [LB18] Congenital anomalies of intestinal fixation Def: A condition caused by failure of the intestines to correctly develop during the antenatal period. This condition may present with intermittent abdominal pain, vomiting, or diarrhoea. Confirmation is t... --PARENT--> [?] Structural developmental anomalies of the digestive tract Def: Any condition caused by failure of the digestive tract to correctly develop during the antenatal period.... --CHILD--> [LB12] Structural developmental anomalies of oesophagus Def: Any congenital defect of oesophagus that results from interference with the normal growth and differentiation of the fetus. Such defects can arise at any stage of embryonic development, vary greatly i... --- Walk 3 --- [DD31.0Z] Non-occlusive mesenteric ischaemia, unspecified --PARENT--> [DD31.0] Non-occlusive mesenteric ischaemia Def: Non-occlusive mesenteric ischaemia causes 20% to 30% of acute mesenteric ischaemia episodes. Mesenteric ischaemia without anatomic arterial or venous obstruction is due to mesenteric vasospasm, which ... --RELATED_TO--> [?] Acute non-occlusive mesenteric arterial ischaemia --- Walk 4 --- [DD31.0Z] Non-occlusive mesenteric ischaemia, unspecified --PARENT--> [DD31.0] Non-occlusive mesenteric ischaemia Def: Non-occlusive mesenteric ischaemia causes 20% to 30% of acute mesenteric ischaemia episodes. Mesenteric ischaemia without anatomic arterial or venous obstruction is due to mesenteric vasospasm, which ... --CHILD--> [DD31.0Z] Non-occlusive mesenteric ischaemia, unspecified --- Walk 5 --- [DD30.0] Acute mesenteric arterial infarction Def: Acute mesenteric arterial infarction is an ischemic disorder of sudden interruption of mesenteric arterial flow because of occlusion of mesenteric artery. This may be further subdivided into acute mes... --PARENT--> [DD30] Acute vascular disorders of intestine Def: Intestinal ischaemia has an associated vascular block, usually due to atheroma, thrombus, or embolus but occasionally the result of an arteritis, vasculitis, or other condition.... --CHILD--> [DD30.0] Acute mesenteric arterial infarction Def: Acute mesenteric arterial infarction is an ischemic disorder of sudden interruption of mesenteric arterial flow because of occlusion of mesenteric artery. This may be further subdivided into acute mes... --- Walk 6 --- [DD30.0] Acute mesenteric arterial infarction Def: Acute mesenteric arterial infarction is an ischemic disorder of sudden interruption of mesenteric arterial flow because of occlusion of mesenteric artery. This may be further subdivided into acute mes... --PARENT--> [DD30] Acute vascular disorders of intestine Def: Intestinal ischaemia has an associated vascular block, usually due to atheroma, thrombus, or embolus but occasionally the result of an arteritis, vasculitis, or other condition.... --CHILD--> [DD30.2] Acute mesenteric venous occlusion Def: Acute mesenteric venous occlusion is an ischemic disorder of sudden interruption of mesenteric venous flow because of venous thrombosis....
[ "[LB18] Congenital anomalies of intestinal fixation\n Def: A condition caused by failure of the intestines to correctly develop during the antenatal period. This condition may present with intermittent abdominal pain, vomiting, or diarrhoea. Confirmation is t...\n --PARENT--> [?] Structural developmental anomalies of the digestive tract\n Def: Any condition caused by failure of the digestive tract to correctly develop during the antenatal period....\n --CHILD--> [LB11] Congenital diverticulum of pharynx\n Def: A condition caused by failure of the pharynx to correctly develop during the antenatal period. This condition may present with difficulty swallowing, or may be asymptomatic. Confirmation is through ob...", "[LB18] Congenital anomalies of intestinal fixation\n Def: A condition caused by failure of the intestines to correctly develop during the antenatal period. This condition may present with intermittent abdominal pain, vomiting, or diarrhoea. Confirmation is t...\n --PARENT--> [?] Structural developmental anomalies of the digestive tract\n Def: Any condition caused by failure of the digestive tract to correctly develop during the antenatal period....\n --CHILD--> [LB12] Structural developmental anomalies of oesophagus\n Def: Any congenital defect of oesophagus that results from interference with the normal growth and differentiation of the fetus. Such defects can arise at any stage of embryonic development, vary greatly i...", "[DD31.0Z] Non-occlusive mesenteric ischaemia, unspecified\n --PARENT--> [DD31.0] Non-occlusive mesenteric ischaemia\n Def: Non-occlusive mesenteric ischaemia causes 20% to 30% of acute mesenteric ischaemia episodes. Mesenteric ischaemia without anatomic arterial or venous obstruction is due to mesenteric vasospasm, which ...\n --RELATED_TO--> [?] Acute non-occlusive mesenteric arterial ischaemia", "[DD31.0Z] Non-occlusive mesenteric ischaemia, unspecified\n --PARENT--> [DD31.0] Non-occlusive mesenteric ischaemia\n Def: Non-occlusive mesenteric ischaemia causes 20% to 30% of acute mesenteric ischaemia episodes. Mesenteric ischaemia without anatomic arterial or venous obstruction is due to mesenteric vasospasm, which ...\n --CHILD--> [DD31.0Z] Non-occlusive mesenteric ischaemia, unspecified", "[DD30.0] Acute mesenteric arterial infarction\n Def: Acute mesenteric arterial infarction is an ischemic disorder of sudden interruption of mesenteric arterial flow because of occlusion of mesenteric artery. This may be further subdivided into acute mes...\n --PARENT--> [DD30] Acute vascular disorders of intestine\n Def: Intestinal ischaemia has an associated vascular block, usually due to atheroma, thrombus, or embolus but occasionally the result of an arteritis, vasculitis, or other condition....\n --CHILD--> [DD30.0] Acute mesenteric arterial infarction\n Def: Acute mesenteric arterial infarction is an ischemic disorder of sudden interruption of mesenteric arterial flow because of occlusion of mesenteric artery. This may be further subdivided into acute mes...", "[DD30.0] Acute mesenteric arterial infarction\n Def: Acute mesenteric arterial infarction is an ischemic disorder of sudden interruption of mesenteric arterial flow because of occlusion of mesenteric artery. This may be further subdivided into acute mes...\n --PARENT--> [DD30] Acute vascular disorders of intestine\n Def: Intestinal ischaemia has an associated vascular block, usually due to atheroma, thrombus, or embolus but occasionally the result of an arteritis, vasculitis, or other condition....\n --CHILD--> [DD30.2] Acute mesenteric venous occlusion\n Def: Acute mesenteric venous occlusion is an ischemic disorder of sudden interruption of mesenteric venous flow because of venous thrombosis...." ]
DC51.Y&XA43V8
Mesentery rupture
[ { "from_icd11": "LB18", "icd10_code": "Q433", "icd10_title": "Congenital malformations of intestinal fixation" }, { "from_icd11": "DD31.0Z", "icd10_code": "K55019", "icd10_title": "Acute (reversible) ischemia of small intestine, extent unspecified" }, { "from_icd11": "DD31.0Z", "icd10_code": "K55029", "icd10_title": "Acute infarction of small intestine, extent unspecified" }, { "from_icd11": "DD31.0Z", "icd10_code": "K55069", "icd10_title": "Acute infarction of intestine, part and extent unspecified" }, { "from_icd11": "DD31.0Z", "icd10_code": "K55021", "icd10_title": "Focal (segmental) acute infarction of small intestine" }, { "from_icd11": "DD31.0Z", "icd10_code": "K55039", "icd10_title": "Acute (reversible) ischemia of large intestine, extent unspecified" }, { "from_icd11": "DD31.0Z", "icd10_code": "K55059", "icd10_title": "Acute (reversible) ischemia of intestine, part and extent unspecified" }, { "from_icd11": "DD31.0Z", "icd10_code": "K55042", "icd10_title": "Diffuse acute infarction of large intestine" }, { "from_icd11": "DD31.0Z", "icd10_code": "K55041", "icd10_title": "Focal (segmental) acute infarction of large intestine" }, { "from_icd11": "DD31.0Z", "icd10_code": "K55011", "icd10_title": "Focal (segmental) acute (reversible) ischemia of small intestine" }, { "from_icd11": "DD31.0Z", "icd10_code": "K55012", "icd10_title": "Diffuse acute (reversible) ischemia of small intestine" }, { "from_icd11": "DD31.0Z", "icd10_code": "K55049", "icd10_title": "Acute infarction of large intestine, extent unspecified" }, { "from_icd11": "DD31.0Z", "icd10_code": "K55061", "icd10_title": "Focal (segmental) acute infarction of intestine, part unspecified" }, { "from_icd11": "DD31.0Z", "icd10_code": "K55022", "icd10_title": "Diffuse acute infarction of small intestine" }, { "from_icd11": "DD31.0Z", "icd10_code": "K55031", "icd10_title": "Focal (segmental) acute (reversible) ischemia of large intestine" } ]
Q433
Congenital malformations of intestinal fixation
The patient was taken in supine position under general anaesthesia. A small longitudinal skin incision 1.5 cm is made proximal upper arm in the upper extremity and fenestration was created in outer cortex of proximal humerus with 3.2 mm drill bit percutaneously under the guidance of image intensifier. An infant feeding tube was inserted to aspirate out the contents of the cyst which were sent for tissue analysis, a larger suction catheter was introduced, and copious irrigation of the bone cyst was carried out. Flexible titanium elastic nail of 3 mm passed through curved end to break the septae and curette the cyst wall, serosanguinous material content of cyst aspirated and collected through suction catheter. Tip of the nail was advanced distally in medullary canal to further decompress the cyst. Finally allogenic Morselized cancellous bone graft prepared and mixed with aspirated bone marrow packed into the cyst cavity through the drill sleeve under the guidance of image intensifier till whole of the cyst was visibly filled with bone graft wound was closed with skin suture and stabilized with “U” slab. Biopsy report confirmed the cyst to be simple bone cyst. The patient was followed up at regular interval, at 10-week follow-up plain skiagram and CT scan showed healing of fracture and resolution of lesion and the patient was able to attain full range of motion at both the shoulder and elbow joint .
3.646484
0.980957
sec[1]/sec[0]/p[1]
en
0.999997
23819089
https://doi.org/10.1155/2013/636197
[ "cyst", "bone", "skin", "drill", "guidance", "intensifier", "suction", "catheter", "nail", "aspirated" ]
[ { "code": "FB80.5", "title": "Solitary bone cyst" }, { "code": "EK70.Z", "title": "Cutaneous cysts, unspecified" }, { "code": "FB4Y", "title": "Other specified disorders of synovium or tendon" }, { "code": "CA0C", "title": "Cyst or mucocele of nose or nasal sinus" }, { "code": "9A7Y", "title": "Other specified disorders of the cornea" }, { "code": "FC0Z", "title": "Diseases of the musculoskeletal system or connective tissue, unspecified" }, { "code": "FB84.Z", "title": "Osteomyelitis or osteitis, unspecified" }, { "code": "FB80.Z", "title": "Disorder of bone density or structure, unspecified" }, { "code": "FB86.11", "title": "Hypertrophy of bone" }, { "code": "FB86.1Z", "title": "Bone hyperplasias, unspecified" } ]
=== ICD-11 CODES FOUND === [FB80.5] Solitary bone cyst Definition: A solitary bone cyst is a benign non-epithelial bone cavity that is asymptomatic and that is found most commonly in the second decade of life by chance. The long bones are most often affected, but cases involving the jaw bone have been reported. Also known as: Solitary bone cyst | cyst of bone | local cyst of bone | simple bone cyst | solitary bone cyst, unspecified site Excludes: solitary cyst of jaw [EK70.Z] Cutaneous cysts, unspecified Also known as: Cutaneous cysts, unspecified | Cutaneous cysts | Follicular cysts of skin and subcutaneous tissue [FB4Y] Other specified disorders of synovium or tendon Also known as: Other specified disorders of synovium or tendon | Shortening of tendon | short tendon | Shortening of tibialis anterior | Contracture of tendon [CA0C] Cyst or mucocele of nose or nasal sinus Definition: A condition which refers to diseases of the nose and nasal sinus that cause a cyst or mucocele. A mucocele is any dilatation (typically pathologic) with accumulation of mucus. Mucoceles are benign, epithelium-lined cysts filled with mucus, which can form in the paranasal sinuses. These structures may cause symptoms if sufficiently large or if exerting pressure on surrounding anatomic structures. Symptomatic mucoceles typically require surgical intervention. Mucoceles should be differentiated fro Also known as: Cyst or mucocele of nose or nasal sinus | cyst of sinus | mucocele of sinus | Cyst of maxillary sinus | cyst of maxillary antrum [9A7Y] Other specified disorders of the cornea Also known as: Other specified disorders of the cornea | Secondary disorders of sclera or cornea | Disorders of sclera and cornea in diseases classified elsewhere | Secondary keratitis or keratoconjunctivitis | Keratitis and keratoconjunctivitis in other diseases classified elsewhere [FC0Z] Diseases of the musculoskeletal system or connective tissue, unspecified Also known as: Diseases of the musculoskeletal system or connective tissue, unspecified | bone disease NOS | bone disorder NOS | bone lesion NOS | musculoskeletal complications NOS [FB84.Z] Osteomyelitis or osteitis, unspecified Also known as: Osteomyelitis or osteitis, unspecified | Osteomyelitis or osteitis | bone inflammation | bone ulcer | bone inflammatory disease [FB80.Z] Disorder of bone density or structure, unspecified Also known as: Disorder of bone density or structure, unspecified | Certain specified disorders of bone density or structure [FB86.11] Hypertrophy of bone Also known as: Hypertrophy of bone | bone thickening | periosteum thickening | Infantile cortical hyperostoses | Post traumatic subperiosteal ossification [FB86.1Z] Bone hyperplasias, unspecified Also known as: Bone hyperplasias, unspecified | Bone hyperplasias === GRAPH WALKS === --- Walk 1 --- [FB80.5] Solitary bone cyst Def: A solitary bone cyst is a benign non-epithelial bone cavity that is asymptomatic and that is found most commonly in the second decade of life by chance. The long bones are most often affected, but cas... --EXCLUDES--> [?] Other cysts of jaw Def: This is mostly odontogenic cysts but may be also of non-odontogenic source. The mandible and maxilla are the bones with the highest prevalent of cysts in the human body owing to odontogenic and develo... --CHILD--> [?] Solitary cyst jaw --- Walk 2 --- [FB80.5] Solitary bone cyst Def: A solitary bone cyst is a benign non-epithelial bone cavity that is asymptomatic and that is found most commonly in the second decade of life by chance. The long bones are most often affected, but cas... --EXCLUDES--> [?] Other cysts of jaw Def: This is mostly odontogenic cysts but may be also of non-odontogenic source. The mandible and maxilla are the bones with the highest prevalent of cysts in the human body owing to odontogenic and develo... --CHILD--> [?] Haemorrhagic cyst of jaw --- Walk 3 --- [EK70.Z] Cutaneous cysts, unspecified --PARENT--> [EK70] Cutaneous cysts --CHILD--> [EK70.2] Digital myxoid pseudocyst Def: Digital myxoid cysts (DMCs) are benign ganglion cysts of the digits, which typically present as a small dome-shaped, often translucent papule on the dorsum of the terminal phalanx and/or as longitudin... --- Walk 4 --- [EK70.Z] Cutaneous cysts, unspecified --PARENT--> [EK70] Cutaneous cysts --CHILD--> [EK70.1] Trichilemmal cyst Def: A trichilemmal (pilar) cyst is a common, typically non-tender, intradermal or subcutaneous cyst. The cysts are typically confined to the scalp and are often multiple. They usually occur sporadically b... --- Walk 5 --- [FB4Y] Other specified disorders of synovium or tendon --PARENT--> [?] Disorders of synovium or tendon Def: This is a group of disorders which affect the synovial joint lining (synovium) and also tendons.... --CHILD--> [FB41] Spontaneous rupture of synovium or tendon Def: This is a spontaneous rupture to a fluid-filled sac containing viscous fluid which normally acts to decrease friction and also provides a cushion between bones and tendons and/or muscles around a join... --- Walk 6 --- [FB4Y] Other specified disorders of synovium or tendon --PARENT--> [?] Disorders of synovium or tendon Def: This is a group of disorders which affect the synovial joint lining (synovium) and also tendons.... --CHILD--> [FB42] Certain specified disorders of synovium or tendon
[ "[FB80.5] Solitary bone cyst\n Def: A solitary bone cyst is a benign non-epithelial bone cavity that is asymptomatic and that is found most commonly in the second decade of life by chance. The long bones are most often affected, but cas...\n --EXCLUDES--> [?] Other cysts of jaw\n Def: This is mostly odontogenic cysts but may be also of non-odontogenic source. The mandible and maxilla are the bones with the highest prevalent of cysts in the human body owing to odontogenic and develo...\n --CHILD--> [?] Solitary cyst jaw", "[FB80.5] Solitary bone cyst\n Def: A solitary bone cyst is a benign non-epithelial bone cavity that is asymptomatic and that is found most commonly in the second decade of life by chance. The long bones are most often affected, but cas...\n --EXCLUDES--> [?] Other cysts of jaw\n Def: This is mostly odontogenic cysts but may be also of non-odontogenic source. The mandible and maxilla are the bones with the highest prevalent of cysts in the human body owing to odontogenic and develo...\n --CHILD--> [?] Haemorrhagic cyst of jaw", "[EK70.Z] Cutaneous cysts, unspecified\n --PARENT--> [EK70] Cutaneous cysts\n --CHILD--> [EK70.2] Digital myxoid pseudocyst\n Def: Digital myxoid cysts (DMCs) are benign ganglion cysts of the digits, which typically present as a small dome-shaped, often translucent papule on the dorsum of the terminal phalanx and/or as longitudin...", "[EK70.Z] Cutaneous cysts, unspecified\n --PARENT--> [EK70] Cutaneous cysts\n --CHILD--> [EK70.1] Trichilemmal cyst\n Def: A trichilemmal (pilar) cyst is a common, typically non-tender, intradermal or subcutaneous cyst. The cysts are typically confined to the scalp and are often multiple. They usually occur sporadically b...", "[FB4Y] Other specified disorders of synovium or tendon\n --PARENT--> [?] Disorders of synovium or tendon\n Def: This is a group of disorders which affect the synovial joint lining (synovium) and also tendons....\n --CHILD--> [FB41] Spontaneous rupture of synovium or tendon\n Def: This is a spontaneous rupture to a fluid-filled sac containing viscous fluid which normally acts to decrease friction and also provides a cushion between bones and tendons and/or muscles around a join...", "[FB4Y] Other specified disorders of synovium or tendon\n --PARENT--> [?] Disorders of synovium or tendon\n Def: This is a group of disorders which affect the synovial joint lining (synovium) and also tendons....\n --CHILD--> [FB42] Certain specified disorders of synovium or tendon" ]
FB80.5
Solitary bone cyst
[ { "from_icd11": "FB80.5", "icd10_code": "M85412", "icd10_title": "Solitary bone cyst, left shoulder" }, { "from_icd11": "FB80.5", "icd10_code": "M85441", "icd10_title": "Solitary bone cyst, right hand" }, { "from_icd11": "FB80.5", "icd10_code": "M8548", "icd10_title": "Solitary bone cyst, other site" }, { "from_icd11": "FB80.5", "icd10_code": "M8540", "icd10_title": "Solitary bone cyst, unspecified site" }, { "from_icd11": "FB80.5", "icd10_code": "M854", "icd10_title": "Solitary bone cyst" }, { "from_icd11": "EK70.Z", "icd10_code": "L729", "icd10_title": "Follicular cyst of the skin and subcutaneous tissue, unspecified" }, { "from_icd11": "EK70.Z", "icd10_code": "L728", "icd10_title": "Other follicular cysts of the skin and subcutaneous tissue" }, { "from_icd11": "EK70.Z", "icd10_code": "L60-L75", "icd10_title": "" }, { "from_icd11": "EK70.Z", "icd10_code": "L72", "icd10_title": "Follicular cysts of skin and subcutaneous tissue" }, { "from_icd11": "CA0C", "icd10_code": "J341", "icd10_title": "Cyst and mucocele of nose and nasal sinus" }, { "from_icd11": "FC0Z", "icd10_code": "XIII", "icd10_title": "" }, { "from_icd11": "FB84.Z", "icd10_code": "M86672", "icd10_title": "Other chronic osteomyelitis, left ankle and foot" }, { "from_icd11": "FB84.Z", "icd10_code": "M86172", "icd10_title": "Other acute osteomyelitis, left ankle and foot" }, { "from_icd11": "FB84.Z", "icd10_code": "M86171", "icd10_title": "Other acute osteomyelitis, right ankle and foot" }, { "from_icd11": "FB84.Z", "icd10_code": "M86671", "icd10_title": "Other chronic osteomyelitis, right ankle and foot" } ]
M85412
Solitary bone cyst, left shoulder
Patient was taken up for surgery under combined supraclavicular block and spinal anaesthesia. Through a dorsal approach over the radial border of ulna, wide resection of distal ulna was performed . The resected ulna measured 8 cm . Around 10 cm of proximal fibula was harvested in routine fashion. The harvested graft was trimmed to fit the distal ulna . Care was taken to position the cartilage surface of fibula facing the radius while the raw surface facing medially as otherwise fusion of the newly constructed DRUJ could occur. The fibular graft was stabilised on the ulnar stump with a 6 holed 3.5 mm narrow dynamic compression plate with 5 screws. To stabilise the distal radioulnar joint, palmaris longus tendon free graft was harvested through two separate stab incisions, one at the level of wrist and the other in the proximal forearm on the volar surface. A drill hole was made across the joint. Palmaris longus tendon was passed through the hole and sutured back on to it . To protect the palmaris longus tenodesis, two K wires were drilled additionally across the DRUJ. To augment the tenodesis, a slip of ECU was sutured to the palmaris longus tenodesis . Wounds were closed in routine fashion and above elbow POP slab was applied with forearm in supination. Sutures were removed on the 12th postoperative day. Histopathological examination of the resected specimen was consistent with giant cell tumour.
3.84375
0.967285
sec[1]/p[2]
en
0.999999
24455371
https://doi.org/10.1155/2013/953149
[ "ulna", "palmaris", "longus", "harvested", "graft", "surface", "tenodesis", "resected", "fibula", "routine" ]
[ { "code": "LB99.3", "title": "Ulnar hemimelia" }, { "code": "FB86.11", "title": "Hypertrophy of bone" }, { "code": "FA31.Y", "title": "Other specified acquired deformities of limbs" }, { "code": "FB80.Y", "title": "Other specified disorders of bone density or structure" }, { "code": "NC32.2", "title": "Fracture of shaft of ulna" }, { "code": "EA90.42", "title": "Palmoplantar pustulosis" }, { "code": "ED55.0", "title": "Acquired palmoplantar keratodermas" }, { "code": "EC20.32", "title": "Papular palmoplantar keratodermas" }, { "code": "1F2D.4", "title": "Tinea nigra" }, { "code": "CA70.0", "title": "Farmer lung" } ]
=== ICD-11 CODES FOUND === [LB99.3] Ulnar hemimelia Definition: Ulnar hemimelia is a congenital ulnar deficiency of the forearm characterised by complete or partial absence of the ulna bone. Also known as: Ulnar hemimelia | Longitudinal reduction defect of ulna | agenesis of ulna | congenital absence of ulna | congenital absence of ulna with or without absence of some distal elements [FB86.11] Hypertrophy of bone Also known as: Hypertrophy of bone | bone thickening | periosteum thickening | Infantile cortical hyperostoses | Post traumatic subperiosteal ossification [FA31.Y] Other specified acquired deformities of limbs Also known as: Other specified acquired deformities of limbs | Acquired deformity of forearm | Deflection of radius | Bowing of the radius | Bowing of forearm [FB80.Y] Other specified disorders of bone density or structure Also known as: Other specified disorders of bone density or structure | Bone dysplasia | Inherited bone dysplasia | Acquired bone dysplasia | Drug-induced bone dysplasia [NC32.2] Fracture of shaft of ulna Also known as: Fracture of shaft of ulna | fracture of ulna | comminuted fracture of shaft of ulna | oblique fracture of shaft of ulna | ulna fracture dislocation [EA90.42] Palmoplantar pustulosis Definition: Palmoplantar pustulosis (PPP) is a chronic inflammatory skin condition characterised by crops of sterile pustules on the palms and soles which erupt repeatedly over months or years. The affected areas tend to become red and scaly; cracks may form and these are often painful. It is strongly associated with smoking. It is associated with psoriasis elsewhere on the body in up to 24% of patients though appears to have a genetic profile distinct from psoriasis vulgaris. Interleukin-36 receptor gene p Also known as: Palmoplantar pustulosis | Palmoplantar pustular psoriasis | Pustulosis palmaris et plantaris | PPP - [palmoplantar pustulosis] | Pustular psoriasis of the palms and soles Includes: Palmoplantar pustular psoriasis [ED55.0] Acquired palmoplantar keratodermas Also known as: Acquired palmoplantar keratodermas | Acquired keratoderma palmaris et plantaris | Keratoderma of palms and soles, acquired | Keratoderma climactericum Excludes: inherited keratosis palmaris et plantaris [EC20.32] Papular palmoplantar keratodermas Definition: Palmoplantar keratoderma characterised by the presence of multiple small discrete hyperkeratotic papules involving palmar and plantar skin. Also known as: Papular palmoplantar keratodermas | Punctate palmoplantar keratoderma | Keratoderma punctata palmaris et plantaris | Buschke-Fischer-Brauer keratoderma | keratosis punctata [1F2D.4] Tinea nigra Definition: A disease of the skin, caused by an infection with the fungi Tinea nigra. This disease is characterised by brown to black macules; small, flat circumscribed changes in the colour of skin. This disease commonly presents on the palmar surfaces, soles, or other skin surfaces. Transmission is by direct contact with contaminated soil, wood, or vegetation. Confirmation is identification of Tinea nigra in a skin sample. Also known as: Tinea nigra | Keratomycosis nigricans palmaris Includes: Keratomycosis nigricans palmaris [CA70.0] Farmer lung Definition: Farmer's lung disease is a hypersensitivity pneumonitis, caused by inhalation of organic dust containing spores of microorganisms, often thermophilic actinomycetes and less commonly Saccharopolyspora rectivirgula, living in mouldy hay, straw, or grain. Typical symptoms include dyspnoea, cough, tiredness, headaches and occasional fever/night sweats, with acute, sub-acute or chronic clinical course and can result in chronic disability with granulomatous disease. Also known as: Farmer lung | farmers' lung | farmers' lung disease | mouldy hay disease | moldy hay disorder === GRAPH WALKS === --- Walk 1 --- [LB99.3] Ulnar hemimelia Def: Ulnar hemimelia is a congenital ulnar deficiency of the forearm characterised by complete or partial absence of the ulna bone.... --PARENT--> [LB99] Reduction defects of upper limb Def: Any condition caused by the failure of an upper limb to correctly develop during the antenatal period. These conditions are characterised by reduction in size or absence of the limb.... --CHILD--> [LB99.1] Humeral agenesis or hypoplasia --- Walk 2 --- [LB99.3] Ulnar hemimelia Def: Ulnar hemimelia is a congenital ulnar deficiency of the forearm characterised by complete or partial absence of the ulna bone.... --PARENT--> [LB99] Reduction defects of upper limb Def: Any condition caused by the failure of an upper limb to correctly develop during the antenatal period. These conditions are characterised by reduction in size or absence of the limb.... --CHILD--> [LB99.1] Humeral agenesis or hypoplasia --- Walk 3 --- [FB86.11] Hypertrophy of bone --PARENT--> [FB86.1] Bone hyperplasias --CHILD--> [FB86.11] Hypertrophy of bone --- Walk 4 --- [FB86.11] Hypertrophy of bone --PARENT--> [FB86.1] Bone hyperplasias --CHILD--> [FB86.1Y] Other specified bone hyperplasias --- Walk 5 --- [FA31.Y] Other specified acquired deformities of limbs --PARENT--> [FA31] Other acquired deformities of limbs --CHILD--> [FA31.2] Flexion deformity --- Walk 6 --- [FA31.Y] Other specified acquired deformities of limbs --PARENT--> [FA31] Other acquired deformities of limbs --EXCLUDES--> [?] Structural developmental anomalies of the skeleton Def: A deformation established before birth of an anatomical structure of one or more bones....
[ "[LB99.3] Ulnar hemimelia\n Def: Ulnar hemimelia is a congenital ulnar deficiency of the forearm characterised by complete or partial absence of the ulna bone....\n --PARENT--> [LB99] Reduction defects of upper limb\n Def: Any condition caused by the failure of an upper limb to correctly develop during the antenatal period. These conditions are characterised by reduction in size or absence of the limb....\n --CHILD--> [LB99.1] Humeral agenesis or hypoplasia", "[LB99.3] Ulnar hemimelia\n Def: Ulnar hemimelia is a congenital ulnar deficiency of the forearm characterised by complete or partial absence of the ulna bone....\n --PARENT--> [LB99] Reduction defects of upper limb\n Def: Any condition caused by the failure of an upper limb to correctly develop during the antenatal period. These conditions are characterised by reduction in size or absence of the limb....\n --CHILD--> [LB99.1] Humeral agenesis or hypoplasia", "[FB86.11] Hypertrophy of bone\n --PARENT--> [FB86.1] Bone hyperplasias\n --CHILD--> [FB86.11] Hypertrophy of bone", "[FB86.11] Hypertrophy of bone\n --PARENT--> [FB86.1] Bone hyperplasias\n --CHILD--> [FB86.1Y] Other specified bone hyperplasias", "[FA31.Y] Other specified acquired deformities of limbs\n --PARENT--> [FA31] Other acquired deformities of limbs\n --CHILD--> [FA31.2] Flexion deformity", "[FA31.Y] Other specified acquired deformities of limbs\n --PARENT--> [FA31] Other acquired deformities of limbs\n --EXCLUDES--> [?] Structural developmental anomalies of the skeleton\n Def: A deformation established before birth of an anatomical structure of one or more bones...." ]
LB99.3
Ulnar hemimelia
[ { "from_icd11": "LB99.3", "icd10_code": "Q715", "icd10_title": "Longitudinal reduction defect of ulna" }, { "from_icd11": "FB86.11", "icd10_code": "M89351", "icd10_title": "Hypertrophy of bone, right femur" }, { "from_icd11": "FB86.11", "icd10_code": "M89361", "icd10_title": "Hypertrophy of bone, right tibia" }, { "from_icd11": "FB86.11", "icd10_code": "M8938", "icd10_title": "Hypertrophy of bone, other site" }, { "from_icd11": "FB86.11", "icd10_code": "M89371", "icd10_title": "Hypertrophy of bone, right ankle and foot" }, { "from_icd11": "FB86.11", "icd10_code": "M89363", "icd10_title": "Hypertrophy of bone, right fibula" }, { "from_icd11": "FB86.11", "icd10_code": "M89333", "icd10_title": "Hypertrophy of bone, right radius" }, { "from_icd11": "FB86.11", "icd10_code": "M89362", "icd10_title": "Hypertrophy of bone, left tibia" }, { "from_icd11": "FB86.11", "icd10_code": "M8930", "icd10_title": "Hypertrophy of bone, unspecified site" }, { "from_icd11": "FB86.11", "icd10_code": "M893", "icd10_title": "Hypertrophy of bone" }, { "from_icd11": "FB80.Y", "icd10_code": "M8580", "icd10_title": "Other specified disorders of bone density and structure, unspecified site" }, { "from_icd11": "FB80.Y", "icd10_code": "M8588", "icd10_title": "Other specified disorders of bone density and structure, other site" }, { "from_icd11": "NC32.2", "icd10_code": "S52252A", "icd10_title": "Displaced comminuted fracture of shaft of ulna, left arm, initial encounter for closed fracture" }, { "from_icd11": "NC32.2", "icd10_code": "S52251B", "icd10_title": "Displaced comminuted fracture of shaft of ulna, right arm, initial encounter for open fracture type I or II" }, { "from_icd11": "NC32.2", "icd10_code": "S52202B", "icd10_title": "Unspecified fracture of shaft of left ulna, initial encounter for open fracture type I or II" } ]
Q715
Longitudinal reduction defect of ulna
The muscular hypotonia persisted and there was feeding difficulty requiring a feeding tube over the first month. The psychomotor development was severely affected and at a neurological examination at 4.5 months the development corresponded to 6 weeks. There was a general hypotonia, the movements of the legs and arms was largely reduced and stereotypical in quality. Eye contact could not be established and she had almost no sound production. She however reacted to sound and light/dark changes. She made no intention to turn over from back to belly and reverse. Spasticity was noted in the legs. A neurometabolic screen was initiated (see below) since the symptoms were considerably more severe than expected. A repeat MRI showed a progressive loss of the white matter and a secondary enlargement of the ventricles. An adequate spectroscopy could not be performed due to the leucodystrophic changes. Over the following months development was largely absent. She was able to swallow formula, but not in sufficient amounts and developed severe growth failure. After a discussion in the Ethical Committee of the hospital, the parents’ request not to put nasogastric feeding tube or gastrostomy was granted (due to the dismal prognosis). The girl passed away at 13 months of age. The autopsy revealed severe wasting of the organs with a body weight of 4850 g. The final cause of death was probably myocardial infarction.
3.964844
0.980957
sec[2]/sec[0]/p[1]
en
0.999997
28427446
https://doi.org/10.1186/s13023-017-0624-2
[ "feeding", "over", "development", "hypotonia", "tube", "legs", "largely", "sound", "changes", "muscular" ]
[ { "code": "MG43.3Z", "title": "Feeding difficulties, unspecified" }, { "code": "MG43.32", "title": "Feeding problem of adult" }, { "code": "MG43.31", "title": "Feeding problem of child" }, { "code": "6B8Z", "title": "Feeding or eating disorders, unspecified" }, { "code": "MG43.30", "title": "Feeding problem of infant" }, { "code": "MB22.5", "title": "Increased goal-directed activity" }, { "code": "DA0E.5Y", "title": "Other specified malocclusion" }, { "code": "5B80.0Z", "title": "Overweight, unspecified" }, { "code": "NE60", "title": "Harmful effects of drugs, medicaments or biological substances, not elsewhere classified" }, { "code": "MG43.1", "title": "Overeating" } ]
=== ICD-11 CODES FOUND === [MG43.3Z] Feeding difficulties, unspecified Also known as: Feeding difficulties, unspecified | Feeding difficulties | difficult feeding | faulty feeding | Feeding difficulties and mismanagement [MG43.32] Feeding problem of adult Also known as: Feeding problem of adult Excludes: Anorexia Nervosa | Bulimia Nervosa | Binge eating disorder [MG43.31] Feeding problem of child Also known as: Feeding problem of child Excludes: Feeding or eating disorders | Anorexia Nervosa | Avoidant-restrictive food intake disorder [6B8Z] Feeding or eating disorders, unspecified Also known as: Feeding or eating disorders, unspecified | Eating disorder, not elsewhere classified | eating disorder NOS [MG43.30] Feeding problem of infant Also known as: Feeding problem of infant Excludes: Feeding problems of newborn | Avoidant-restrictive food intake disorder [MB22.5] Increased goal-directed activity Definition: Increased planning of and participation in multiple activities (e.g. sexual, occupational, political, religious), compared to the individual's typical level of activity. Also known as: Increased goal-directed activity | overactivity | behaviour of overactivity [DA0E.5Y] Other specified malocclusion Also known as: Other specified malocclusion | Crossbite | overbite | openbite | excessive overbite Includes: Crossbite [5B80.0Z] Overweight, unspecified Also known as: Overweight, unspecified | Overweight [NE60] Harmful effects of drugs, medicaments or biological substances, not elsewhere classified Also known as: Harmful effects of drugs, medicaments or biological substances, not elsewhere classified | drugs, medicaments or biological substances, toxicity not elsewhere classified | adverse drug effects | drug reaction NOS | drug allergy NOS Excludes: Alcohol intoxication | pathological drug intoxication | hypersensitivity reaction to correctly administered drug [MG43.1] Overeating Definition: The consumption of excess food in relation to energy and nutritional requirements. Also known as: Overeating | Excessive eating | gluttony | hyperalimentation | Hyperalimentation NOS Includes: Excessive eating Excludes: Bipolar or related disorders | Depressive disorders | Feeding or eating disorders === GRAPH WALKS === --- Walk 1 --- [MG43.3Z] Feeding difficulties, unspecified --PARENT--> [MG43.3] Feeding difficulties --PARENT--> [MG43] Symptoms or signs concerning food or fluid intake Def: Symptoms or signs concerning food and fluid intake include anorexia, polydipsia, polyphagia, feeding difficulties or mismanagement, abnormal weight loss, abnormal weight gain, insufficient intake of f... --- Walk 2 --- [MG43.3Z] Feeding difficulties, unspecified --PARENT--> [MG43.3] Feeding difficulties --EXCLUDES--> [?] Feeding problems of newborn Def: A lack of interest in feeding or a problem receiving the proper amount of nutrition in a newborn.... --- Walk 3 --- [MG43.32] Feeding problem of adult --EXCLUDES--> [?] Bulimia Nervosa Def: Bulimia Nervosa is characterised by frequent, recurrent episodes of binge eating (e.g. once a week or more over a period of at least one month). A binge eating episode is a distinct period of time dur... --EXCLUDES--> [?] Binge eating disorder Def: Binge eating disorder is characterised by frequent, recurrent episodes of binge eating (e.g. once a week or more over a period of several months). A binge eating episode is a distinct period of time d... --- Walk 4 --- [MG43.32] Feeding problem of adult --EXCLUDES--> [?] Bulimia Nervosa Def: Bulimia Nervosa is characterised by frequent, recurrent episodes of binge eating (e.g. once a week or more over a period of at least one month). A binge eating episode is a distinct period of time dur... --EXCLUDES--> [?] Binge eating disorder Def: Binge eating disorder is characterised by frequent, recurrent episodes of binge eating (e.g. once a week or more over a period of several months). A binge eating episode is a distinct period of time d... --- Walk 5 --- [MG43.31] Feeding problem of child --EXCLUDES--> [?] Anorexia Nervosa Def: Anorexia Nervosa is characterised by significantly low body weight for the individual’s height, age and developmental stage that is not due to another health condition or to the unavailability of food... --EXCLUDES--> [?] Anorexia Def: Anorexia is a pathological lack or loss of appetite.... --- Walk 6 --- [MG43.31] Feeding problem of child --EXCLUDES--> [?] Feeding or eating disorders Def: Feeding and Eating Disorders involve abnormal eating or feeding behaviours that are not explained by another health condition and are not developmentally appropriate or culturally sanctioned. Feeding ... --CHILD--> [?] Anorexia Nervosa Def: Anorexia Nervosa is characterised by significantly low body weight for the individual’s height, age and developmental stage that is not due to another health condition or to the unavailability of food...
[ "[MG43.3Z] Feeding difficulties, unspecified\n --PARENT--> [MG43.3] Feeding difficulties\n --PARENT--> [MG43] Symptoms or signs concerning food or fluid intake\n Def: Symptoms or signs concerning food and fluid intake include anorexia, polydipsia, polyphagia, feeding difficulties or mismanagement, abnormal weight loss, abnormal weight gain, insufficient intake of f...", "[MG43.3Z] Feeding difficulties, unspecified\n --PARENT--> [MG43.3] Feeding difficulties\n --EXCLUDES--> [?] Feeding problems of newborn\n Def: A lack of interest in feeding or a problem receiving the proper amount of nutrition in a newborn....", "[MG43.32] Feeding problem of adult\n --EXCLUDES--> [?] Bulimia Nervosa\n Def: Bulimia Nervosa is characterised by frequent, recurrent episodes of binge eating (e.g. once a week or more over a period of at least one month). A binge eating episode is a distinct period of time dur...\n --EXCLUDES--> [?] Binge eating disorder\n Def: Binge eating disorder is characterised by frequent, recurrent episodes of binge eating (e.g. once a week or more over a period of several months). A binge eating episode is a distinct period of time d...", "[MG43.32] Feeding problem of adult\n --EXCLUDES--> [?] Bulimia Nervosa\n Def: Bulimia Nervosa is characterised by frequent, recurrent episodes of binge eating (e.g. once a week or more over a period of at least one month). A binge eating episode is a distinct period of time dur...\n --EXCLUDES--> [?] Binge eating disorder\n Def: Binge eating disorder is characterised by frequent, recurrent episodes of binge eating (e.g. once a week or more over a period of several months). A binge eating episode is a distinct period of time d...", "[MG43.31] Feeding problem of child\n --EXCLUDES--> [?] Anorexia Nervosa\n Def: Anorexia Nervosa is characterised by significantly low body weight for the individual’s height, age and developmental stage that is not due to another health condition or to the unavailability of food...\n --EXCLUDES--> [?] Anorexia\n Def: Anorexia is a pathological lack or loss of appetite....", "[MG43.31] Feeding problem of child\n --EXCLUDES--> [?] Feeding or eating disorders\n Def: Feeding and Eating Disorders involve abnormal eating or feeding behaviours that are not explained by another health condition and are not developmentally appropriate or culturally sanctioned. Feeding ...\n --CHILD--> [?] Anorexia Nervosa\n Def: Anorexia Nervosa is characterised by significantly low body weight for the individual’s height, age and developmental stage that is not due to another health condition or to the unavailability of food..." ]
MG43.3Z
Feeding difficulties, unspecified
[ { "from_icd11": "MG43.3Z", "icd10_code": "R633", "icd10_title": "Feeding difficulties" }, { "from_icd11": "6B8Z", "icd10_code": "F5082", "icd10_title": "Avoidant/restrictive food intake disorder" }, { "from_icd11": "6B8Z", "icd10_code": "F5089", "icd10_title": "Other specified eating disorder" }, { "from_icd11": "6B8Z", "icd10_code": "F5081", "icd10_title": "Binge eating disorder" }, { "from_icd11": "6B8Z", "icd10_code": "F9829", "icd10_title": "Other feeding disorders of infancy and early childhood" }, { "from_icd11": "6B8Z", "icd10_code": "F9821", "icd10_title": "Rumination disorder of infancy" }, { "from_icd11": "6B8Z", "icd10_code": "F508", "icd10_title": "Other eating disorders" }, { "from_icd11": "6B8Z", "icd10_code": "F509", "icd10_title": "Eating disorder, unspecified" }, { "from_icd11": "6B8Z", "icd10_code": "F50", "icd10_title": "Eating disorders" }, { "from_icd11": "6B8Z", "icd10_code": "F504", "icd10_title": "" }, { "from_icd11": "6B8Z", "icd10_code": "F505", "icd10_title": "" }, { "from_icd11": "6B8Z", "icd10_code": "F982", "icd10_title": "Other feeding disorders of infancy and childhood" }, { "from_icd11": "MB22.5", "icd10_code": "R463", "icd10_title": "Overactivity" }, { "from_icd11": "5B80.0Z", "icd10_code": "E669", "icd10_title": "Obesity, unspecified" }, { "from_icd11": "NE60", "icd10_code": "T50A95A", "icd10_title": "Adverse effect of other bacterial vaccines, initial encounter" } ]
R633
Feeding difficulties
Deep Sequencing, or Next Generation Sequencing (NGS), is a powerful tool to identify causative variants in clinical cases, where other methods have been exhausted. Here, we describe a 4-year-old male, born at full term following an uneventful pregnancy and delivery to non-consanguineous parents, and four siblings presented with generalized seizure at the age of 9 days. Upon ruling out all other major etiologies for seizures, initial evaluation identified severe hypocalcemia of 5.7 mg/dl [9–11], hyperphosphatemia of 11.5 mg/dl [5–9], and inappropriately low PTH of 20.7, alongside normal albumin, magnesium, potassium, chloride, blood gases, and vitamin D levels. Urinary calcium levels were low at 0.18 mg/dl [5.2–35.7]. Physical examination revealed no dysmorphic features, short stature, malformations, or developmental delay. Additional studies included chest X-ray, brain US, echocardiogram, renal ultrasound, electroencephalogram, bone age study, and audiogram were all normal. Following a clinical geneticist consultation, 22q11.2 deletion was ruled out via Fluorescent In-Situ Hybridization (FISH). Sanger Sequencing detected no genomic variants in PTH and GCM2 genes. Since no additional loci were related to the phenotype, array-CGH was not performed. Fig. 1 Family pedigree. Squares denote male family members, circles female members, and shaded symbols affected members; the arrow points to the proband
4.101563
0.928223
sec[0]/p[0]
en
0.999996
28444561
https://doi.org/10.1007/s00439-017-1804-9
[ "sequencing", "members", "variants", "additional", "family", "next", "generation", "powerful", "tool", "identify" ]
[ { "code": "LB73.10", "title": "Poland syndrome" }, { "code": "LD44.N0", "title": "CATCH 22 phenotype" }, { "code": "LB31.3", "title": "Exstrophy of urinary bladder" }, { "code": "LD2F.1Y", "title": "Other specified syndromes with multiple structural anomalies, not of environmental origin" }, { "code": "LA56", "title": "Pierre Robin syndrome" }, { "code": "QE60", "title": "Absence of family member" }, { "code": "QE61", "title": "Disappearance or death of family member" }, { "code": "QE50.4", "title": "Relationship with parents, in-laws or other family members" }, { "code": "QE70.2", "title": "Dependent relative needing care at home" }, { "code": "QE61.Y", "title": "Disappearance or death of other family member" } ]
=== ICD-11 CODES FOUND === [LB73.10] Poland syndrome Definition: Poland syndrome is characterised by a unilateral absence or hypoplasia of the pectoralis major muscle (most frequently involving the sternocostal portion), and a variable degree of ipsilateral hand anomalies, including symbrachydactyly. Also known as: Poland syndrome | Poland sequence | Poland anomaly [LD44.N0] CATCH 22 phenotype Definition: Monosomy 22q11 (DiGeorge Velocardiofacial syndrome, DGS/VCF) syndrome is a chromosomal anomaly characterised by the association of several variable malformations: hypoplastic thymus and parathyroid glands, congenital conotruncal heart defects, a subtle but characteristic facial dysmorphism, cleft palate or velar insufficiency, and learning difficulties. Also known as: CATCH 22 phenotype | Conotruncal anomalies face syndrome | Velocardiofacial syndrome | Shprintzen syndrome | Sedlackova syndrome Includes: Pharyngeal pouch syndrome | DiGeorge syndrome | Velocardiofacial syndrome [LB31.3] Exstrophy of urinary bladder Definition: Bladder exstrophy (or classic bladder exstrophy) is a congenital genitourinary malformation belonging to the spectrum of the exstrophy-epispadias complex and is characterised by an evaginated bladder plate, epispadias and an anterior defect of the pelvis, pelvic floor and abdominal wall. Also known as: Exstrophy of urinary bladder | Ectopia vesicae | Extroversion of bladder | bladder ectopia | congenital ectopic bladder Includes: Ectopia vesicae | Extroversion of bladder [LD2F.1Y] Other specified syndromes with multiple structural anomalies, not of environmental origin Also known as: Other specified syndromes with multiple structural anomalies, not of environmental origin | 46,XX disorder of sex development - anorectal anomalies | 46,XX DSD - anorectal anomalies | Aarskog-Scott syndrome | Aarskog syndrome [LA56] Pierre Robin syndrome Definition: Pierre-Robin syndrome (or Pierre-Robin sequence) is characterised by triad of orofacial morphological anomalies consisting of retrognathism, glossoptosis and a posterior median velopalatal cleft. This condition is referred to as a sequence because the posterior cleft palate is a secondary defect associated with abnormal mandibular development: mandibular hypoplasia occurring early in gestation causes the tongue to be maintained high-up in the oral cavity, preventing fusion of the palatal shelves Also known as: Pierre Robin syndrome | Pierre Robin sequence [QE60] Absence of family member Also known as: Absence of family member [QE61] Disappearance or death of family member Also known as: Disappearance or death of family member | assumed death of family member | death of family member | disappearance of family member Excludes: Prolonged grief disorder [QE50.4] Relationship with parents, in-laws or other family members Also known as: Relationship with parents, in-laws or other family members | Problems in relationship with parents | problem with parent | Problem with aged parent | Problem with sibling Excludes: Caregiver-child relationship problem | Problems associated with upbringing | Problem associated with interactions with spouse or partner [QE70.2] Dependent relative needing care at home Also known as: Dependent relative needing care at home | Sick or handicapped person in family needing care at home | Anxiety (normal) about sick person in family | Ill or disturbed family member [QE61.Y] Disappearance or death of other family member Also known as: Disappearance or death of other family member === GRAPH WALKS === --- Walk 1 --- [LB73.10] Poland syndrome Def: Poland syndrome is characterised by a unilateral absence or hypoplasia of the pectoralis major muscle (most frequently involving the sternocostal portion), and a variable degree of ipsilateral hand an... --PARENT--> [LB73.1] Structural developmental anomalies of chest wall Def: Any condition caused by failure of the chest wall to correctly develop during the antenatal period.... --CHILD--> [LB73.10] Poland syndrome Def: Poland syndrome is characterised by a unilateral absence or hypoplasia of the pectoralis major muscle (most frequently involving the sternocostal portion), and a variable degree of ipsilateral hand an... --- Walk 2 --- [LB73.10] Poland syndrome Def: Poland syndrome is characterised by a unilateral absence or hypoplasia of the pectoralis major muscle (most frequently involving the sternocostal portion), and a variable degree of ipsilateral hand an... --PARENT--> [LB73.1] Structural developmental anomalies of chest wall Def: Any condition caused by failure of the chest wall to correctly develop during the antenatal period.... --PARENT--> [LB73] Structural developmental anomalies of spine or bony thorax Def: Any condition caused by failure of the spine or bony thorax to correctly develop during the antenatal period.... --- Walk 3 --- [LD44.N0] CATCH 22 phenotype Def: Monosomy 22q11 (DiGeorge Velocardiofacial syndrome, DGS/VCF) syndrome is a chromosomal anomaly characterised by the association of several variable malformations: hypoplastic thymus and parathyroid gl... --PARENT--> [LD44.N] Deletions of chromosome 22 --CHILD--> [LD44.N0] CATCH 22 phenotype Def: Monosomy 22q11 (DiGeorge Velocardiofacial syndrome, DGS/VCF) syndrome is a chromosomal anomaly characterised by the association of several variable malformations: hypoplastic thymus and parathyroid gl... --- Walk 4 --- [LD44.N0] CATCH 22 phenotype Def: Monosomy 22q11 (DiGeorge Velocardiofacial syndrome, DGS/VCF) syndrome is a chromosomal anomaly characterised by the association of several variable malformations: hypoplastic thymus and parathyroid gl... --PARENT--> [LD44.N] Deletions of chromosome 22 --CHILD--> [LD44.NZ] Deletions of chromosome 22, unspecified --- Walk 5 --- [LB31.3] Exstrophy of urinary bladder Def: Bladder exstrophy (or classic bladder exstrophy) is a congenital genitourinary malformation belonging to the spectrum of the exstrophy-epispadias complex and is characterised by an evaginated bladder ... --PARENT--> [LB31] Structural developmental anomalies of urinary tract Def: Any condition caused by failure of the urinary tract to correctly develop during the antenatal period.... --CHILD--> [LB31.1] Congenital primary megaureter Def: Congenital primary megaureter is an idiopathic condition in which the bladder and bladder outlet are normal but the ureter is dilated to some extent. It may be obstructed, refluxing or unobstructed an... --- Walk 6 --- [LB31.3] Exstrophy of urinary bladder Def: Bladder exstrophy (or classic bladder exstrophy) is a congenital genitourinary malformation belonging to the spectrum of the exstrophy-epispadias complex and is characterised by an evaginated bladder ... --PARENT--> [LB31] Structural developmental anomalies of urinary tract Def: Any condition caused by failure of the urinary tract to correctly develop during the antenatal period.... --CHILD--> [LB31.2] Fetal lower urinary tract obstruction Def: A disease caused by partial or complete obstruction of the urethra, during the antenatal period. This disease can present with enlarged bladder, oligohydramnios, or pulmonary hypoplasia. Confirmation ...
[ "[LB73.10] Poland syndrome\n Def: Poland syndrome is characterised by a unilateral absence or hypoplasia of the pectoralis major muscle (most frequently involving the sternocostal portion), and a variable degree of ipsilateral hand an...\n --PARENT--> [LB73.1] Structural developmental anomalies of chest wall\n Def: Any condition caused by failure of the chest wall to correctly develop during the antenatal period....\n --CHILD--> [LB73.10] Poland syndrome\n Def: Poland syndrome is characterised by a unilateral absence or hypoplasia of the pectoralis major muscle (most frequently involving the sternocostal portion), and a variable degree of ipsilateral hand an...", "[LB73.10] Poland syndrome\n Def: Poland syndrome is characterised by a unilateral absence or hypoplasia of the pectoralis major muscle (most frequently involving the sternocostal portion), and a variable degree of ipsilateral hand an...\n --PARENT--> [LB73.1] Structural developmental anomalies of chest wall\n Def: Any condition caused by failure of the chest wall to correctly develop during the antenatal period....\n --PARENT--> [LB73] Structural developmental anomalies of spine or bony thorax\n Def: Any condition caused by failure of the spine or bony thorax to correctly develop during the antenatal period....", "[LD44.N0] CATCH 22 phenotype\n Def: Monosomy 22q11 (DiGeorge Velocardiofacial syndrome, DGS/VCF) syndrome is a chromosomal anomaly characterised by the association of several variable malformations: hypoplastic thymus and parathyroid gl...\n --PARENT--> [LD44.N] Deletions of chromosome 22\n --CHILD--> [LD44.N0] CATCH 22 phenotype\n Def: Monosomy 22q11 (DiGeorge Velocardiofacial syndrome, DGS/VCF) syndrome is a chromosomal anomaly characterised by the association of several variable malformations: hypoplastic thymus and parathyroid gl...", "[LD44.N0] CATCH 22 phenotype\n Def: Monosomy 22q11 (DiGeorge Velocardiofacial syndrome, DGS/VCF) syndrome is a chromosomal anomaly characterised by the association of several variable malformations: hypoplastic thymus and parathyroid gl...\n --PARENT--> [LD44.N] Deletions of chromosome 22\n --CHILD--> [LD44.NZ] Deletions of chromosome 22, unspecified", "[LB31.3] Exstrophy of urinary bladder\n Def: Bladder exstrophy (or classic bladder exstrophy) is a congenital genitourinary malformation belonging to the spectrum of the exstrophy-epispadias complex and is characterised by an evaginated bladder ...\n --PARENT--> [LB31] Structural developmental anomalies of urinary tract\n Def: Any condition caused by failure of the urinary tract to correctly develop during the antenatal period....\n --CHILD--> [LB31.1] Congenital primary megaureter\n Def: Congenital primary megaureter is an idiopathic condition in which the bladder and bladder outlet are normal but the ureter is dilated to some extent. It may be obstructed, refluxing or unobstructed an...", "[LB31.3] Exstrophy of urinary bladder\n Def: Bladder exstrophy (or classic bladder exstrophy) is a congenital genitourinary malformation belonging to the spectrum of the exstrophy-epispadias complex and is characterised by an evaginated bladder ...\n --PARENT--> [LB31] Structural developmental anomalies of urinary tract\n Def: Any condition caused by failure of the urinary tract to correctly develop during the antenatal period....\n --CHILD--> [LB31.2] Fetal lower urinary tract obstruction\n Def: A disease caused by partial or complete obstruction of the urethra, during the antenatal period. This disease can present with enlarged bladder, oligohydramnios, or pulmonary hypoplasia. Confirmation ..." ]
LB73.10
Poland syndrome
[ { "from_icd11": "LD44.N0", "icd10_code": "D821", "icd10_title": "Di George's syndrome" }, { "from_icd11": "LB31.3", "icd10_code": "Q6412", "icd10_title": "Cloacal exstrophy of urinary bladder" }, { "from_icd11": "LB31.3", "icd10_code": "Q6419", "icd10_title": "Other exstrophy of urinary bladder" }, { "from_icd11": "LB31.3", "icd10_code": "Q6410", "icd10_title": "Exstrophy of urinary bladder, unspecified" }, { "from_icd11": "LB31.3", "icd10_code": "Q64", "icd10_title": "Other congenital malformations of urinary system" }, { "from_icd11": "LB31.3", "icd10_code": "Q641", "icd10_title": "Exstrophy of urinary bladder" }, { "from_icd11": "LA56", "icd10_code": "Q870", "icd10_title": "Congenital malformation syndromes predominantly affecting facial appearance" }, { "from_icd11": "QE60", "icd10_code": "Z6332", "icd10_title": "Other absence of family member" }, { "from_icd11": "QE60", "icd10_code": "Z633", "icd10_title": "Absence of family member" }, { "from_icd11": "QE61", "icd10_code": "Z634", "icd10_title": "Disappearance and death of family member" }, { "from_icd11": "QE50.4", "icd10_code": "Z601", "icd10_title": "" }, { "from_icd11": "QE50.4", "icd10_code": "Z631", "icd10_title": "Problems in relationship with in-laws" }, { "from_icd11": "QE70.2", "icd10_code": "Z636", "icd10_title": "Dependent relative needing care at home" } ]
D821
Di George's syndrome
Endoscopic retrograde cholangiography and 3-dimensional computed tomography cholangiography found abrupt narrowing of the common hepatic duct that was 20 mm in length including the right and left hepatic ducts, with involvement of the right anterior and posterior bile duct bifurcations . Adenocarcinoma was evident by the cytological findings, and this was confirmed by brush cytology. Contrast enhanced computed tomography (CECT) showed no distant metastases or lymph node metastases. We diagnosed these findings as Bismuth type 4, T2N0M0 Stage II hilar cholangiocarcinoma. According to the preoperative imaging findings, the left bile duct was completely occluded by cancer, there was narrowing of right hepatic duct and anterior sector bile duct, and only the right posterior bile duct was free from the margin. Therefore, we planned left trisectionectomy, extrahepatic bile duct resection, and Roux-en-Y choledochojejunostomy. Fig. 1 Endoscopic retrograde cholangiography ( a ) and 3-dimensional CT cholangiography ( b , c , d ) reveals stenosis of the common hepatic duct that was 20 mm in length including the right and left hepatic ducts, with involvement of the right anterior (arrow) and posterior (arrow head) bile duct bifurcation. The pattern of confluence of the right posterior hepatic artery is of the supra-portal type. The left hepatic duct is completely occluded by cancer and could not be identified
4.003906
0.940918
sec[1]/p[1]
en
0.999996
30249240
https://doi.org/10.1186/s12893-018-0415-2
[ "duct", "hepatic", "bile", "cholangiography", "endoscopic", "retrograde", "dimensional", "computed", "tomography", "narrowing" ]
[ { "code": "DC10.02", "title": "Obstruction of bile duct" }, { "code": "DC10.00", "title": "Obstruction of cystic duct" }, { "code": "DC13", "title": "Cholangitis" }, { "code": "LB20.23", "title": "Structural developmental anomalies of cystic duct" }, { "code": "DC10.2", "title": "Fistula of gallbladder or bile duct" }, { "code": "DB9Z", "title": "Diseases of liver, unspecified" }, { "code": "DB97.Z", "title": "Inflammatory liver disease, unspecified" }, { "code": "DB99.7", "title": "Hepatic failure without mention whether acute or chronic" }, { "code": "LB20.0Y", "title": "Other specified structural developmental anomalies of liver" }, { "code": "LB20.0Z", "title": "Structural developmental anomalies of liver, unspecified" } ]
=== ICD-11 CODES FOUND === [DC10.02] Obstruction of bile duct Also known as: Obstruction of bile duct | extrahepatic biliary obstruction | extrahepatic bile duct obstruction | bile duct obstruction | bile stasis Excludes: with cholelithiasis [DC10.00] Obstruction of cystic duct Also known as: Obstruction of cystic duct | cystic duct obstruction | cystic ductal obstruction | obstructed cystic duct | Acquired cystic duct atresia [DC13] Cholangitis Also known as: Cholangitis | acute cholangiolitis | ascending cholangitis | cholangiolitis | cholangitis NOS Excludes: chronic nonsuppurative destructive cholangitis | cholangitis with cholelithiasis | Primary sclerosing cholangitis [LB20.23] Structural developmental anomalies of cystic duct Also known as: Structural developmental anomalies of cystic duct | congenital deformity of cystic duct | cystic duct anomaly | cystic duct deformity | cystic duct distortion [DC10.2] Fistula of gallbladder or bile duct Definition: This is an abnormal connection or passageway between gallbladder or bile duct and other organs. Also known as: Fistula of gallbladder or bile duct | fistula of gallbladder | gallbladder fistula | Cholecystocolic fistula | Cholecystoduodenal fistula [DB9Z] Diseases of liver, unspecified Also known as: Diseases of liver, unspecified | liver disease | liver condition NOS | organ liver disease | hepatopathy [DB97.Z] Inflammatory liver disease, unspecified Also known as: Inflammatory liver disease, unspecified | Certain specified inflammatory liver diseases | Nonspecific reactive hepatitis | inflammatory liver disease | hepatitis NOS [DB99.7] Hepatic failure without mention whether acute or chronic Also known as: Hepatic failure without mention whether acute or chronic | liver decompensation | liver function failure | hepatic failure NOS | liver failure NOS [LB20.0Y] Other specified structural developmental anomalies of liver Also known as: Other specified structural developmental anomalies of liver | Alagille syndrome | Alagille-Watson syndrome | Arteriohepatic dysplasia | Syndromic bile duct paucity [LB20.0Z] Structural developmental anomalies of liver, unspecified Also known as: Structural developmental anomalies of liver, unspecified | Structural developmental anomalies of liver | Malformations of liver | congenital anomaly of liver | congenital malformation of liver === GRAPH WALKS === --- Walk 1 --- [DC10.02] Obstruction of bile duct --EXCLUDES--> [?] Cholelithiasis Def: Cholelithiasis is calculus of gallbladder, cystic duct or bile duct. Most stones in the gallbladder are asymptomatic, but the most common initial symptom is biliary colic before the development of com... --CHILD--> [?] Mirizzi syndrome Def: This is a rare complication in which a gallstone becomes impacted in the cystic duct or neck of the gallbladder causing compression of the common bile duct (CBD) or common hepatic duct, resulting in o... --- Walk 2 --- [DC10.02] Obstruction of bile duct --EXCLUDES--> [?] Cholelithiasis Def: Cholelithiasis is calculus of gallbladder, cystic duct or bile duct. Most stones in the gallbladder are asymptomatic, but the most common initial symptom is biliary colic before the development of com... --CHILD--> [?] Mirizzi syndrome Def: This is a rare complication in which a gallstone becomes impacted in the cystic duct or neck of the gallbladder causing compression of the common bile duct (CBD) or common hepatic duct, resulting in o... --- Walk 3 --- [DC10.00] Obstruction of cystic duct --PARENT--> [DC10.0] Obstruction of gallbladder or bile ducts Def: This is obstruction in the small organ that aids mainly in fat digestion and concentrates bile produced by the liver and in any of a number of long tube-like structures that carry bile.... --CHILD--> [DC10.00] Obstruction of cystic duct --- Walk 4 --- [DC10.00] Obstruction of cystic duct --PARENT--> [DC10.0] Obstruction of gallbladder or bile ducts Def: This is obstruction in the small organ that aids mainly in fat digestion and concentrates bile produced by the liver and in any of a number of long tube-like structures that carry bile.... --CHILD--> [DC10.00] Obstruction of cystic duct --- Walk 5 --- [DC13] Cholangitis --EXCLUDES--> [?] Calculus of bile duct with cholangitis Def: Stones in bile duct present with inflammation of bile duct.... --CHILD--> [?] Calculus of bile duct with acute cholangitis Def: Stones in bile duct present with acute inflammation of bile duct.... --- Walk 6 --- [DC13] Cholangitis --EXCLUDES--> [?] Primary sclerosing cholangitis Def: Primary sclerosing cholangitis is a chronic disease which shows focal or multifocal strictures of intra- and/or extra-hepatic bile ducts without any apparent causes, leading to cholestasis and ultimat... --PARENT--> [?] Autoimmune liver disease Def: Autoimmune liver diseases are generally forms of chronic liver disease in which the etiology is unclear but autoimmune mechanisms are evident or postulated for the development of the disease. The prim...
[ "[DC10.02] Obstruction of bile duct\n --EXCLUDES--> [?] Cholelithiasis\n Def: Cholelithiasis is calculus of gallbladder, cystic duct or bile duct. Most stones in the gallbladder are asymptomatic, but the most common initial symptom is biliary colic before the development of com...\n --CHILD--> [?] Mirizzi syndrome\n Def: This is a rare complication in which a gallstone becomes impacted in the cystic duct or neck of the gallbladder causing compression of the common bile duct (CBD) or common hepatic duct, resulting in o...", "[DC10.02] Obstruction of bile duct\n --EXCLUDES--> [?] Cholelithiasis\n Def: Cholelithiasis is calculus of gallbladder, cystic duct or bile duct. Most stones in the gallbladder are asymptomatic, but the most common initial symptom is biliary colic before the development of com...\n --CHILD--> [?] Mirizzi syndrome\n Def: This is a rare complication in which a gallstone becomes impacted in the cystic duct or neck of the gallbladder causing compression of the common bile duct (CBD) or common hepatic duct, resulting in o...", "[DC10.00] Obstruction of cystic duct\n --PARENT--> [DC10.0] Obstruction of gallbladder or bile ducts\n Def: This is obstruction in the small organ that aids mainly in fat digestion and concentrates bile produced by the liver and in any of a number of long tube-like structures that carry bile....\n --CHILD--> [DC10.00] Obstruction of cystic duct", "[DC10.00] Obstruction of cystic duct\n --PARENT--> [DC10.0] Obstruction of gallbladder or bile ducts\n Def: This is obstruction in the small organ that aids mainly in fat digestion and concentrates bile produced by the liver and in any of a number of long tube-like structures that carry bile....\n --CHILD--> [DC10.00] Obstruction of cystic duct", "[DC13] Cholangitis\n --EXCLUDES--> [?] Calculus of bile duct with cholangitis\n Def: Stones in bile duct present with inflammation of bile duct....\n --CHILD--> [?] Calculus of bile duct with acute cholangitis\n Def: Stones in bile duct present with acute inflammation of bile duct....", "[DC13] Cholangitis\n --EXCLUDES--> [?] Primary sclerosing cholangitis\n Def: Primary sclerosing cholangitis is a chronic disease which shows focal or multifocal strictures of intra- and/or extra-hepatic bile ducts without any apparent causes, leading to cholestasis and ultimat...\n --PARENT--> [?] Autoimmune liver disease\n Def: Autoimmune liver diseases are generally forms of chronic liver disease in which the etiology is unclear but autoimmune mechanisms are evident or postulated for the development of the disease. The prim..." ]
DC10.02
Obstruction of bile duct
[ { "from_icd11": "DC10.02", "icd10_code": "K831", "icd10_title": "Obstruction of bile duct" }, { "from_icd11": "DC13", "icd10_code": "K8309", "icd10_title": "Other cholangitis" }, { "from_icd11": "DC13", "icd10_code": "K8301", "icd10_title": "Primary sclerosing cholangitis" }, { "from_icd11": "DC13", "icd10_code": "K830", "icd10_title": "Cholangitis" }, { "from_icd11": "DC10.2", "icd10_code": "K833", "icd10_title": "Fistula of bile duct" }, { "from_icd11": "DC10.2", "icd10_code": "K823", "icd10_title": "Fistula of gallbladder" }, { "from_icd11": "DB9Z", "icd10_code": "K7681", "icd10_title": "Hepatopulmonary syndrome" }, { "from_icd11": "DB9Z", "icd10_code": "K7689", "icd10_title": "Other specified diseases of liver" }, { "from_icd11": "DB9Z", "icd10_code": "K769", "icd10_title": "Liver disease, unspecified" }, { "from_icd11": "DB9Z", "icd10_code": "K77", "icd10_title": "Liver disorders in diseases classified elsewhere" }, { "from_icd11": "DB9Z", "icd10_code": "K762", "icd10_title": "Central hemorrhagic necrosis of liver" }, { "from_icd11": "DB9Z", "icd10_code": "K70-K77", "icd10_title": "" }, { "from_icd11": "DB9Z", "icd10_code": "K778", "icd10_title": "" }, { "from_icd11": "DB9Z", "icd10_code": "K72", "icd10_title": "Hepatic failure, not elsewhere classified" }, { "from_icd11": "DB9Z", "icd10_code": "K76", "icd10_title": "Other diseases of liver" } ]
K831
Obstruction of bile duct
During the operation, the nodule could not be visualized by the standard white light DaVinci endoscope . The endoscope was then toggled to a near-infrared mode that allows highlighting of any lesions that fluoresce over 800 nm (“Firefly mode”). Upon toggling to the Firefly mode, the nodule in the mediastinum was visualized. A Medtronic Visionsense Iridium system was also tested to identify the lesion . The lesion and surrounding tissue was excised without difficulty without extending the magnitude of the operation because of the localization by FGS. After excision, the nodule was visualized with a near-infrared microscope and fluorescence as identified in the lesion but not the normal surrounding fat . The ratio of fluorescence from the lesion to the fat was 6.3 (ImageJ, NIH). Fig. 3 White light imaging of the mediastinum showed no obvious sign of the mediastinal lesion. The anterior mediastinum, vena cava and heart are seen from the perspective of the right hemithorax Fig. 4 White light imaging did not reveal the location of the diseased tissue in the anterior mediastinum. However, near-infrared imaging localized the abnormal tissue distinctly for the surgeon to do a targeted resection Fig. 5 On the back table, the fluorescence from the abnormal tissue which was a suspected lymph node contrasted well from the surrounding fatty tissues. The ratio of fluorescence from the lesion to the fat was 6.3
3.931641
0.641113
sec[1]/p[4]
en
0.999997
PMC9734605
https://doi.org/10.1186/s13019-022-02054-8
[ "lesion", "mediastinum", "tissue", "fluorescence", "nodule", "visualized", "white", "light", "near", "infrared" ]
[ { "code": "FA5Z", "title": "Arthropathies, unspecified" }, { "code": "FC0Z", "title": "Diseases of the musculoskeletal system or connective tissue, unspecified" }, { "code": "ME60.Z", "title": "Skin lesion of unspecified nature" }, { "code": "MD41", "title": "Clinical findings on diagnostic imaging of lung" }, { "code": "GC2Z&XA6KU8", "title": "Disease of kidney, not elsewhere classified" }, { "code": "CB22.Z", "title": "Disease of mediastinum, unspecified" }, { "code": "CA44", "title": "Pyothorax" }, { "code": "CB22.Y", "title": "Other specified diseases of mediastinum, not elsewhere classified" }, { "code": "2F91.Y&XA7WA2", "title": "Neoplasms of unknown behaviour of mediastinum" }, { "code": "CB22.0", "title": "Fibrosing mediastinitis" } ]
=== ICD-11 CODES FOUND === [FA5Z] Arthropathies, unspecified Also known as: Arthropathies, unspecified | Disorders affecting predominantly peripheral joints | Disorders affecting predominantly peripheral limb joints | arthropathy NOS | arthropathic [FC0Z] Diseases of the musculoskeletal system or connective tissue, unspecified Also known as: Diseases of the musculoskeletal system or connective tissue, unspecified | bone disease NOS | bone disorder NOS | bone lesion NOS | musculoskeletal complications NOS [ME60.Z] Skin lesion of unspecified nature Also known as: Skin lesion of unspecified nature | Skin lesion of uncertain or unspecified nature | Skin lesion without established diagnosis | Pigmented skin lesion of unspecified nature | Ulcer of skin of unspecified nature [MD41] Clinical findings on diagnostic imaging of lung Definition: Clinical findings on diagnostic imaging of lung is findings on diagnostic imaging of the lung which don't appear in normal status of the body. Diagnostic imaging refers to technologies that doctors use to look inside body for clues about a medical condition. X-rays, CT scans, nuclear medicine scans, MRI scans and ultrasound are all types of diagnostic imaging. Also known as: Clinical findings on diagnostic imaging of lung | abnormal diagnostic imaging of lung | Hyperinflation of lung | Lung mass | Pulmonary lobe mass [CB22.Z] Disease of mediastinum, unspecified Also known as: Disease of mediastinum, unspecified | Diseases of mediastinum, not elsewhere classified | disease of mediastinum | disorder of mediastinum | mediastinal disease [CA44] Pyothorax Definition: Suppurative inflammation of the pleural space, typically due to acute bacterial infection. It can occur as a complication of pneumonia, thoracotomy, abscesses (lung, hepatic, or subdiaphragmatic), or penetrating trauma with a secondary infection. Also known as: Pyothorax | empyema | pyopneumothorax | Pyothorax with fistula | empyema with fistula Includes: empyema | pyopneumothorax Excludes: due to tuberculosis [CB22.Y] Other specified diseases of mediastinum, not elsewhere classified Also known as: Other specified diseases of mediastinum, not elsewhere classified | Hernia of mediastinum | mediastinal hernia | mediastinal herniation | Infectious mediastinitis [CB22.0] Fibrosing mediastinitis Definition: Fibrosing mediastinitis, also known as sclerosing mediastinitis or mediastinal fibrosis, is a disorder characterised by an excessive fibrotic reaction in the mediastinum. It can result in compromise of airways, great vessels, and other mediastinal structures, with morbidity directly related to the location and extent of fibrosis. The commonest cause is histoplasmosis, of which it is a rare late complication, but it may also occur in association with other infections and with systemic autoimmune Also known as: Fibrosing mediastinitis | mediastinal fibrosis | idiopathic mediastinal fibrosis | Histoplasmosis-related fibrosing mediastinitis | Histoplasmosis-related mediastinal fibrosis mediastinitis === GRAPH WALKS === --- Walk 1 --- [FA5Z] Arthropathies, unspecified --PARENT--> [?] Arthropathies --CHILD--> [?] Infection related arthropathies Def: A disease of the joints, caused by an infection with a bacterial, viral, fungal, or parasitic source. Distinction is made between the following types of etiological relationship. a) direct infection ... --- Walk 2 --- [FA5Z] Arthropathies, unspecified --PARENT--> [?] Arthropathies --CHILD--> [?] Osteoarthritis Def: Osteoarthritis (OA) can be defined as a group of distinct, but overlapping diseases, which may have different etiologies, but similar biological, morphological, and clinical outcomes affecting the art... --- Walk 3 --- [FC0Z] Diseases of the musculoskeletal system or connective tissue, unspecified --PARENT--> [15] Diseases of the musculoskeletal system or connective tissue Def: This chapter contains diseases of musculoskeletal system and diseases of connective tissue.... --RELATED_TO--> [?] Symptoms, signs or clinical findings of the musculoskeletal system --- Walk 4 --- [FC0Z] Diseases of the musculoskeletal system or connective tissue, unspecified --PARENT--> [15] Diseases of the musculoskeletal system or connective tissue Def: This chapter contains diseases of musculoskeletal system and diseases of connective tissue.... --RELATED_TO--> [?] Symptoms, signs or clinical findings of the musculoskeletal system --- Walk 5 --- [ME60.Z] Skin lesion of unspecified nature --PARENT--> [ME60] Skin lesion of uncertain or unspecified nature Def: To be used where there is either significant uncertainty or alternatively no information as to the nature of a circumscribed skin lesion. This is of particular importance with regard to whether or not... --CHILD--> [ME60.2] Ulcer of skin of uncertain nature Def: This denotes the presence of a skin ulcer but uncertainty as to its nature. No inference as to whether the ulcer might be of serious significance (e.g. suspected skin cancer) is made.... --- Walk 6 --- [ME60.Z] Skin lesion of unspecified nature --PARENT--> [ME60] Skin lesion of uncertain or unspecified nature Def: To be used where there is either significant uncertainty or alternatively no information as to the nature of a circumscribed skin lesion. This is of particular importance with regard to whether or not... --CHILD--> [ME60.1] Pigmented skin lesion of uncertain nature Def: This denotes the presence of a pigmented skin lesion but uncertainty as to its nature. No inference as to whether the lesion might be of serious significance (e.g. suspected skin cancer) is made....
[ "[FA5Z] Arthropathies, unspecified\n --PARENT--> [?] Arthropathies\n --CHILD--> [?] Infection related arthropathies\n Def: A disease of the joints, caused by an infection with a bacterial, viral, fungal, or parasitic source.\n\nDistinction is made between the following types of etiological relationship.\na) direct infection ...", "[FA5Z] Arthropathies, unspecified\n --PARENT--> [?] Arthropathies\n --CHILD--> [?] Osteoarthritis\n Def: Osteoarthritis (OA) can be defined as a group of distinct, but overlapping diseases, which may have different etiologies, but similar biological, morphological, and clinical outcomes affecting the art...", "[FC0Z] Diseases of the musculoskeletal system or connective tissue, unspecified\n --PARENT--> [15] Diseases of the musculoskeletal system or connective tissue\n Def: This chapter contains diseases of musculoskeletal system and diseases of connective tissue....\n --RELATED_TO--> [?] Symptoms, signs or clinical findings of the musculoskeletal system", "[FC0Z] Diseases of the musculoskeletal system or connective tissue, unspecified\n --PARENT--> [15] Diseases of the musculoskeletal system or connective tissue\n Def: This chapter contains diseases of musculoskeletal system and diseases of connective tissue....\n --RELATED_TO--> [?] Symptoms, signs or clinical findings of the musculoskeletal system", "[ME60.Z] Skin lesion of unspecified nature\n --PARENT--> [ME60] Skin lesion of uncertain or unspecified nature\n Def: To be used where there is either significant uncertainty or alternatively no information as to the nature of a circumscribed skin lesion. This is of particular importance with regard to whether or not...\n --CHILD--> [ME60.2] Ulcer of skin of uncertain nature\n Def: This denotes the presence of a skin ulcer but uncertainty as to its nature. No inference as to whether the ulcer might be of serious significance (e.g. suspected skin cancer) is made....", "[ME60.Z] Skin lesion of unspecified nature\n --PARENT--> [ME60] Skin lesion of uncertain or unspecified nature\n Def: To be used where there is either significant uncertainty or alternatively no information as to the nature of a circumscribed skin lesion. This is of particular importance with regard to whether or not...\n --CHILD--> [ME60.1] Pigmented skin lesion of uncertain nature\n Def: This denotes the presence of a pigmented skin lesion but uncertainty as to its nature. No inference as to whether the lesion might be of serious significance (e.g. suspected skin cancer) is made...." ]
FA5Z
Arthropathies, unspecified
[ { "from_icd11": "FA5Z", "icd10_code": "M00-M25", "icd10_title": "" }, { "from_icd11": "FC0Z", "icd10_code": "XIII", "icd10_title": "" }, { "from_icd11": "ME60.Z", "icd10_code": "L989", "icd10_title": "Disorder of the skin and subcutaneous tissue, unspecified" }, { "from_icd11": "MD41", "icd10_code": "R911", "icd10_title": "Solitary pulmonary nodule" }, { "from_icd11": "MD41", "icd10_code": "R91", "icd10_title": "Abnormal findings on diagnostic imaging of lung" }, { "from_icd11": "CB22.Z", "icd10_code": "J9859", "icd10_title": "Other diseases of mediastinum, not elsewhere classified" }, { "from_icd11": "CB22.Z", "icd10_code": "J9851", "icd10_title": "Mediastinitis" }, { "from_icd11": "CB22.Z", "icd10_code": "J985", "icd10_title": "Diseases of mediastinum, not elsewhere classified" }, { "from_icd11": "CA44", "icd10_code": "J869", "icd10_title": "Pyothorax without fistula" }, { "from_icd11": "CA44", "icd10_code": "J860", "icd10_title": "Pyothorax with fistula" }, { "from_icd11": "CA44", "icd10_code": "J85-J86", "icd10_title": "" }, { "from_icd11": "CA44", "icd10_code": "J86", "icd10_title": "Pyothorax" } ]
M00-M25
In each case the mass was closely associated with visible residual staples even when there was no luminal connection. The cytology of the mucus was unremarkable. Histology showed normal rectal mucosa in each case with only some surrounding fibrosis. Figure 1 shows an MRI along with the findings on colonoscopy and operative appearance of the pararectal mass in the same patient which was located laterally between the 2 o’clock and 5 o’clock positions in lithotomy with a size of 3.3 × 4.5 cm. In this case, the mass extended above the levator floor, the mass was performed with the incision procedure. Only two patients were assessed with repeat MRI examination one week after surgery and the postoperative course of all patients was unremarkable with all cases asymptomatic at a one-year follow-up. Fig. 1 MRI, colonoscopic and operative findings of the lateral pararectal mass in the same patient. A Sagittal image showing a large mucocele without sphincteric involvement ( A ). Image B confirms the mucocele locale and dimensions on axial MRI. B On flexible endoscopy the mucocele appears as a pararectal submucosal mass without any luminal connexion. C Clear mucoid material was evacuated from the mass. D The operative specimen included part of the rectal mucocele with visible rectal mucosa and retained staples. F Operative view in which the mucocele was formally opened and marsupialized with the rectal lumen
3.966797
0.824707
sec[2]/p[1]
en
0.999998
PMC9341070
https://doi.org/10.1186/s12893-022-01744-3
[ "mucocele", "rectal", "pararectal", "visible", "staples", "luminal", "unremarkable", "mucosa", "which", "clock" ]
[ { "code": "CA0C", "title": "Cyst or mucocele of nose or nasal sinus" }, { "code": "CA0C&XA8817", "title": "Mucocele of turbinate" }, { "code": "9A23.1", "title": "Acquired orbital cyst" }, { "code": "DB11.6", "title": "Mucocele of appendix" }, { "code": "DA04.5", "title": "Mucocele of salivary gland" }, { "code": "DB30.4", "title": "Stenosis of the rectum" }, { "code": "DB31.0&XA4KU2", "title": "Rectal fistula" }, { "code": "NB91.91", "title": "Laceration of rectum" }, { "code": "2F90.1", "title": "Neoplasms of unknown behaviour of rectum" }, { "code": "DB32.2Z&XA4KU2", "title": "Rectal dilatation" } ]
=== ICD-11 CODES FOUND === [CA0C] Cyst or mucocele of nose or nasal sinus Definition: A condition which refers to diseases of the nose and nasal sinus that cause a cyst or mucocele. A mucocele is any dilatation (typically pathologic) with accumulation of mucus. Mucoceles are benign, epithelium-lined cysts filled with mucus, which can form in the paranasal sinuses. These structures may cause symptoms if sufficiently large or if exerting pressure on surrounding anatomic structures. Symptomatic mucoceles typically require surgical intervention. Mucoceles should be differentiated fro Also known as: Cyst or mucocele of nose or nasal sinus | cyst of sinus | mucocele of sinus | Cyst of maxillary sinus | cyst of maxillary antrum [9A23.1] Acquired orbital cyst Also known as: Acquired orbital cyst | Hydatic cyst | Primary optic nerve sheath cyst | Mucocele of orbit | Hematic cyst of orbit [DB11.6] Mucocele of appendix Definition: Mucocele of the appendix is a cystic, dilated appendix filled with mucin. Simple mucocele is not a neoplasm and results from chronic obstruction of the proximal lumen, usually by fibrous tissue. Also known as: Mucocele of appendix | appendicular mucocele | appendiceal mucocele [DA04.5] Mucocele of salivary gland Definition: This is a clinical term used to describe a bluish, soft, often fluctuant swelling caused by either blockage or rupture of a salivary gland duct. Also known as: Mucocele of salivary gland | retention cyst of salivary gland | salivary cyst | salivary gland mucocele | sialocele [DB30.4] Stenosis of the rectum Definition: Rectal stenosis is defined as narrowing of the rectum. Also known as: Stenosis of the rectum | obstructed rectum | rectal stenosis | stricture of rectum | rectal obstruction [NB91.91] Laceration of rectum Also known as: Laceration of rectum [2F90.1] Neoplasms of unknown behaviour of rectum Also known as: Neoplasms of unknown behaviour of rectum | rectum tumour NOS === GRAPH WALKS === --- Walk 1 --- [CA0C] Cyst or mucocele of nose or nasal sinus Def: A condition which refers to diseases of the nose and nasal sinus that cause a cyst or mucocele. A mucocele is any dilatation (typically pathologic) with accumulation of mucus. Mucoceles are benign, ep... --PARENT--> [?] Upper respiratory tract disorders Def: This group of disorders refers to diseases of the upper airways (upper respiratory tract). The upper airways anatomically are complicated structures which extend from the airway openings at the nares ... --CHILD--> [CA00] Acute nasopharyngitis Def: A disease of the upper respiratory tract, caused by an infection with rhinovirus. This disease is characterised by pharyngitis, runny nose, stuffy nose, or cough. Transmission is by inhalation of infe... --- Walk 2 --- [CA0C] Cyst or mucocele of nose or nasal sinus Def: A condition which refers to diseases of the nose and nasal sinus that cause a cyst or mucocele. A mucocele is any dilatation (typically pathologic) with accumulation of mucus. Mucoceles are benign, ep... --PARENT--> [?] Upper respiratory tract disorders Def: This group of disorders refers to diseases of the upper airways (upper respiratory tract). The upper airways anatomically are complicated structures which extend from the airway openings at the nares ... --EXCLUDES--> [?] Chronic obstructive pulmonary disease with acute exacerbation, unspecified Def: An acute unspecified exacerbation of COPD is an acute event characterised by a worsening of the patient’s respiratory symptoms that is beyond normal day-to-day variations and leads to a change in medi... --- Walk 3 --- [9A23.1] Acquired orbital cyst --RELATED_TO--> [?] Epidermoid cyst Def: A cutaneous cyst with an epidermoid wall filled with keratin and its breakdown products. It most commonly forms as the result of squamous metaplasia in a damaged sebaceous gland but may result from tr... --PARENT--> [?] Acquired orbital cyst --- Walk 4 --- [9A23.1] Acquired orbital cyst --RELATED_TO--> [?] Epidermoid cyst Def: A cutaneous cyst with an epidermoid wall filled with keratin and its breakdown products. It most commonly forms as the result of squamous metaplasia in a damaged sebaceous gland but may result from tr... --PARENT--> [?] Cutaneous cysts --- Walk 5 --- [DB11.6] Mucocele of appendix Def: Mucocele of the appendix is a cystic, dilated appendix filled with mucin. Simple mucocele is not a neoplasm and results from chronic obstruction of the proximal lumen, usually by fibrous tissue.... --PARENT--> [DB11] Certain specified diseases of appendix Def: Diseases of appendix other than appendicitis or neoplasm. This includes intussusception, mucocele, hyperplasia, appendicular concretions, diverticulum, fistula and other specified diseases of appendix... --CHILD--> [DB11.0] Megaloappendix Def: The vermiform appendix is an organ that can have variable sizes, locations as well as functional potentials. This refers to the longer and the larger appendix than normal size.... --- Walk 6 --- [DB11.6] Mucocele of appendix Def: Mucocele of the appendix is a cystic, dilated appendix filled with mucin. Simple mucocele is not a neoplasm and results from chronic obstruction of the proximal lumen, usually by fibrous tissue.... --PARENT--> [DB11] Certain specified diseases of appendix Def: Diseases of appendix other than appendicitis or neoplasm. This includes intussusception, mucocele, hyperplasia, appendicular concretions, diverticulum, fistula and other specified diseases of appendix... --EXCLUDES--> [?] Neoplasms of the appendix Def: An abnormal tumour that form in tissues lining the appendix....
[ "[CA0C] Cyst or mucocele of nose or nasal sinus\n Def: A condition which refers to diseases of the nose and nasal sinus that cause a cyst or mucocele.\nA mucocele is any dilatation (typically pathologic) with accumulation of mucus. Mucoceles are benign, ep...\n --PARENT--> [?] Upper respiratory tract disorders\n Def: This group of disorders refers to diseases of the upper airways (upper respiratory tract). The upper airways anatomically are complicated structures which extend from the airway openings at the nares ...\n --CHILD--> [CA00] Acute nasopharyngitis\n Def: A disease of the upper respiratory tract, caused by an infection with rhinovirus. This disease is characterised by pharyngitis, runny nose, stuffy nose, or cough. Transmission is by inhalation of infe...", "[CA0C] Cyst or mucocele of nose or nasal sinus\n Def: A condition which refers to diseases of the nose and nasal sinus that cause a cyst or mucocele.\nA mucocele is any dilatation (typically pathologic) with accumulation of mucus. Mucoceles are benign, ep...\n --PARENT--> [?] Upper respiratory tract disorders\n Def: This group of disorders refers to diseases of the upper airways (upper respiratory tract). The upper airways anatomically are complicated structures which extend from the airway openings at the nares ...\n --EXCLUDES--> [?] Chronic obstructive pulmonary disease with acute exacerbation, unspecified\n Def: An acute unspecified exacerbation of COPD is an acute event characterised by a worsening of the patient’s respiratory symptoms that is beyond normal day-to-day variations and leads to a change in medi...", "[9A23.1] Acquired orbital cyst\n --RELATED_TO--> [?] Epidermoid cyst\n Def: A cutaneous cyst with an epidermoid wall filled with keratin and its breakdown products. It most commonly forms as the result of squamous metaplasia in a damaged sebaceous gland but may result from tr...\n --PARENT--> [?] Acquired orbital cyst", "[9A23.1] Acquired orbital cyst\n --RELATED_TO--> [?] Epidermoid cyst\n Def: A cutaneous cyst with an epidermoid wall filled with keratin and its breakdown products. It most commonly forms as the result of squamous metaplasia in a damaged sebaceous gland but may result from tr...\n --PARENT--> [?] Cutaneous cysts", "[DB11.6] Mucocele of appendix\n Def: Mucocele of the appendix is a cystic, dilated appendix filled with mucin. Simple mucocele is not a neoplasm and results from chronic obstruction of the proximal lumen, usually by fibrous tissue....\n --PARENT--> [DB11] Certain specified diseases of appendix\n Def: Diseases of appendix other than appendicitis or neoplasm. This includes intussusception, mucocele, hyperplasia, appendicular concretions, diverticulum, fistula and other specified diseases of appendix...\n --CHILD--> [DB11.0] Megaloappendix\n Def: The vermiform appendix is an organ that can have variable sizes, locations as well as functional potentials. This refers to the longer and the larger appendix than normal size....", "[DB11.6] Mucocele of appendix\n Def: Mucocele of the appendix is a cystic, dilated appendix filled with mucin. Simple mucocele is not a neoplasm and results from chronic obstruction of the proximal lumen, usually by fibrous tissue....\n --PARENT--> [DB11] Certain specified diseases of appendix\n Def: Diseases of appendix other than appendicitis or neoplasm. This includes intussusception, mucocele, hyperplasia, appendicular concretions, diverticulum, fistula and other specified diseases of appendix...\n --EXCLUDES--> [?] Neoplasms of the appendix\n Def: An abnormal tumour that form in tissues lining the appendix...." ]
CA0C
Cyst or mucocele of nose or nasal sinus
[ { "from_icd11": "CA0C", "icd10_code": "J341", "icd10_title": "Cyst and mucocele of nose and nasal sinus" }, { "from_icd11": "DA04.5", "icd10_code": "K116", "icd10_title": "Mucocele of salivary gland" }, { "from_icd11": "DB30.4", "icd10_code": "K624", "icd10_title": "Stenosis of anus and rectum" }, { "from_icd11": "2F90.1", "icd10_code": "D375", "icd10_title": "Neoplasm of uncertain behavior of rectum" } ]
J341
Cyst and mucocele of nose and nasal sinus
We present the case of a 75-year-old male whom initially presented to our service with a mass on his right upper back. The patient's medical history included coronary artery disease and hyperlipidemia. Further history revealed he had received (2) stents in the past and undergone multiple heart catheterizations (up to seven) approximately seven years prior at an outside facility. During his last catheterization and stent procedure, which took over 4 hours (approx. 33 mSv), he developed a radiation-induced injury to his right back around the T10 dermatome ( Figure 1(a) ). During the following years, the burn was closely followed at an outside facility, and the area developed a chronic nonhealing ulcer which continued to evolve over time eventually growing outward from his back and developing a foul odor on his presentation to our facility in 2017. He reported increasing pain at the periphery of the tumor margin. Up to a year prior to presentation, the area was flat and biopsies revealed no evidence of malignancy. Upon presentation to us, however, the physical exam demonstrated a fungating mass approximately 5 × 9 cm with central purulent necrosis and induration surrounding the periphery (Figures 1(b) – 1(d) ). No additional nodularity or adenopathy was found on physical exam initially. At this time, punch biopsies demonstrated undifferentiated pleomorphic sarcoma along with frankly necrotic debris.
3.84375
0.986328
sec[1]/p[0]
en
0.999996
30174980
https://doi.org/10.1155/2018/2903801
[ "back", "facility", "initially", "seven", "approximately", "outside", "which", "over", "area", "time" ]
[ { "code": "ND51.0", "title": "Dislocation or strain or sprain of unspecified joint or ligament of trunk" }, { "code": "ME84.Z", "title": "Spinal pain, unspecified" }, { "code": "ND51.Y", "title": "Other specified injuries of spine or trunk, level unspecified" }, { "code": "FB10", "title": "Spinal instabilities" }, { "code": "FA70.0", "title": "Kyphosis" }, { "code": "QB14", "title": "Unavailability or inaccessibility of health care facilities" }, { "code": "QB1Z", "title": "Factors related to medical facilities or other health care, unspecified" }, { "code": "QB10", "title": "Medical services not available in home" }, { "code": "QB15", "title": "Medical services not available in current medical facility" }, { "code": "QB1Y", "title": "Other specified factors related to medical facilities or other health care" } ]
=== ICD-11 CODES FOUND === [ND51.0] Dislocation or strain or sprain of unspecified joint or ligament of trunk Also known as: Dislocation or strain or sprain of unspecified joint or ligament of trunk | Back dislocation | Back sprain | Back strain | Dislocation of vertebra, not elsewhere classified [ME84.Z] Spinal pain, unspecified Also known as: Spinal pain, unspecified | Spinal pain | joint stiffness of spine | Dorsalgia | back ache [ND51.Y] Other specified injuries of spine or trunk, level unspecified Also known as: Other specified injuries of spine or trunk, level unspecified | Superficial injury of trunk, level unspecified | multiple superficial injuries of trunk | Abrasion of trunk, level unspecified | Contusion of trunk, level unspecified [FB10] Spinal instabilities Also known as: Spinal instabilities | spinal instabilities, site unspecified | spinal instability | instability of back | relaxation of back ligaments Excludes: Spondylolysis [FA70.0] Kyphosis Definition: This is a curving of the spine that causes a bowing or rounding of the back, which leads to a hunchback or slouching posture. Also known as: Kyphosis | postural kyphosis | Kyphosis with no determinant | primary kyphosis | idiopathic kyphosis Excludes: Post radiation kyphosis [QB14] Unavailability or inaccessibility of health care facilities Also known as: Unavailability or inaccessibility of health care facilities | unavailability of medical facilities | Unavailability of outpatient clinic | Unavailability or inaccessibility of residential aged care service Excludes: bed unavailable [QB1Z] Factors related to medical facilities or other health care, unspecified Also known as: Factors related to medical facilities or other health care, unspecified | Health care problem, not elsewhere classified | Medical facilities problem, not elsewhere classified [QB10] Medical services not available in home Also known as: Medical services not available in home | unavailability of medical facilities in home Excludes: Difficulty or need for assistance with activities [QB15] Medical services not available in current medical facility Also known as: Medical services not available in current medical facility [QB1Y] Other specified factors related to medical facilities or other health care Also known as: Other specified factors related to medical facilities or other health care | Transfer for suspected condition === GRAPH WALKS === --- Walk 1 --- [ND51.0] Dislocation or strain or sprain of unspecified joint or ligament of trunk --RELATED_TO--> [?] Fracture, dislocation or subluxation of spine due to birth injury Def: A true fracture of the spine is very rare due to birth injury. A fracture is usually in the cervical area and follows a difficult footling breech vaginal delivery. Dislocation refers to the displaceme... --PARENT--> [?] Birth injury to skeleton Def: A condition characterised by the presence of damage to the skeleton due to physical pressure or injury during delivery.... --- Walk 2 --- [ND51.0] Dislocation or strain or sprain of unspecified joint or ligament of trunk --PARENT--> [ND51] Other injuries of spine or trunk, level unspecified --CHILD--> [ND51.0] Dislocation or strain or sprain of unspecified joint or ligament of trunk --- Walk 3 --- [ME84.Z] Spinal pain, unspecified --PARENT--> [ME84] Spinal pain Def: This is a condition characterised by pain felt in the back that usually originates from the muscles, nerves, bones, joints or other structures in the spine.... --EXCLUDES--> [?] Chronic neuropathic pain Def: Chronic neuropathic pain is chronic pain caused by a lesion or disease of the somatosensory nervous system. The pain may be spontaneous or evoked, as an increased response to a painful stimulus (hyper... --- Walk 4 --- [ME84.Z] Spinal pain, unspecified --PARENT--> [ME84] Spinal pain Def: This is a condition characterised by pain felt in the back that usually originates from the muscles, nerves, bones, joints or other structures in the spine.... --CHILD--> [ME84.2] Low back pain Def: This is a condition which is defined as pain and discomfort, localised below the costal margin and above the inferior gluteal folds, with or without leg pain.... --- Walk 5 --- [ND51.Y] Other specified injuries of spine or trunk, level unspecified --PARENT--> [ND51] Other injuries of spine or trunk, level unspecified --EXCLUDES--> [?] Crushing injuries involving multiple body regions --- Walk 6 --- [ND51.Y] Other specified injuries of spine or trunk, level unspecified --PARENT--> [ND51] Other injuries of spine or trunk, level unspecified --PARENT--> [?] Injuries to unspecified part of trunk, limb or body region
[ "[ND51.0] Dislocation or strain or sprain of unspecified joint or ligament of trunk\n --RELATED_TO--> [?] Fracture, dislocation or subluxation of spine due to birth injury\n Def: A true fracture of the spine is very rare due to birth injury. A fracture is usually in the cervical area and follows a difficult footling breech vaginal delivery. Dislocation refers to the displaceme...\n --PARENT--> [?] Birth injury to skeleton\n Def: A condition characterised by the presence of damage to the skeleton due to physical pressure or injury during delivery....", "[ND51.0] Dislocation or strain or sprain of unspecified joint or ligament of trunk\n --PARENT--> [ND51] Other injuries of spine or trunk, level unspecified\n --CHILD--> [ND51.0] Dislocation or strain or sprain of unspecified joint or ligament of trunk", "[ME84.Z] Spinal pain, unspecified\n --PARENT--> [ME84] Spinal pain\n Def: This is a condition characterised by pain felt in the back that usually originates from the muscles, nerves, bones, joints or other structures in the spine....\n --EXCLUDES--> [?] Chronic neuropathic pain\n Def: Chronic neuropathic pain is chronic pain caused by a lesion or disease of the somatosensory nervous system. The pain may be spontaneous or evoked, as an increased response to a painful stimulus (hyper...", "[ME84.Z] Spinal pain, unspecified\n --PARENT--> [ME84] Spinal pain\n Def: This is a condition characterised by pain felt in the back that usually originates from the muscles, nerves, bones, joints or other structures in the spine....\n --CHILD--> [ME84.2] Low back pain\n Def: This is a condition which is defined as pain and discomfort, localised below the costal margin and above the inferior gluteal folds, with or without leg pain....", "[ND51.Y] Other specified injuries of spine or trunk, level unspecified\n --PARENT--> [ND51] Other injuries of spine or trunk, level unspecified\n --EXCLUDES--> [?] Crushing injuries involving multiple body regions", "[ND51.Y] Other specified injuries of spine or trunk, level unspecified\n --PARENT--> [ND51] Other injuries of spine or trunk, level unspecified\n --PARENT--> [?] Injuries to unspecified part of trunk, limb or body region" ]
ND51.0
Dislocation or strain or sprain of unspecified joint or ligament of trunk
[ { "from_icd11": "ND51.0", "icd10_code": "T092", "icd10_title": "" }, { "from_icd11": "ME84.Z", "icd10_code": "M5489", "icd10_title": "Other dorsalgia" }, { "from_icd11": "ME84.Z", "icd10_code": "M5481", "icd10_title": "Occipital neuralgia" }, { "from_icd11": "ME84.Z", "icd10_code": "M5408", "icd10_title": "Panniculitis affecting regions of neck and back, sacral and sacrococcygeal region" }, { "from_icd11": "ME84.Z", "icd10_code": "M549", "icd10_title": "Dorsalgia, unspecified" }, { "from_icd11": "ME84.Z", "icd10_code": "M54", "icd10_title": "Dorsalgia" }, { "from_icd11": "ME84.Z", "icd10_code": "M540", "icd10_title": "Panniculitis affecting regions of neck and back" }, { "from_icd11": "ME84.Z", "icd10_code": "M548", "icd10_title": "Other dorsalgia" }, { "from_icd11": "ND51.Y", "icd10_code": "S30860A", "icd10_title": "Insect bite (nonvenomous) of lower back and pelvis, initial encounter" }, { "from_icd11": "ND51.Y", "icd10_code": "S30861A", "icd10_title": "Insect bite (nonvenomous) of abdominal wall, initial encounter" }, { "from_icd11": "FB10", "icd10_code": "M532X2", "icd10_title": "Spinal instabilities, cervical region" }, { "from_icd11": "FB10", "icd10_code": "M532X9", "icd10_title": "Spinal instabilities, site unspecified" }, { "from_icd11": "FB10", "icd10_code": "M532X6", "icd10_title": "Spinal instabilities, lumbar region" }, { "from_icd11": "FB10", "icd10_code": "M532X4", "icd10_title": "Spinal instabilities, thoracic region" }, { "from_icd11": "FB10", "icd10_code": "M532X8", "icd10_title": "Spinal instabilities, sacral and sacrococcygeal region" } ]
T092
An emergency operation for the head injury was performed, and the ACJ injury was simultaneously fixed with a hook plate . On the second day after the procedure, SCJ dislocation was noticed during a radiological review. Closed reduction with a clamp was attempted, but grasping the clavicle was impossible due to excessive subcutaneous emphysema. The patient underwent open reduction. The reduction was performed without any difficulty by directly holding the clavicle with a clamp. The clavicle's position could be maintained without any support, but it was easily redislocated when compression force was applied to the medial clavicle. Surgical augmentation with reinforced, braided, polyethylene-blended sutures (FiberWire®, Arthrex, Naples, FL, USA) was performed. Three sutures were passed through a drilled hole on the clavicle; then, holes were made in the manubrium, as Thomas et al. described. Sutures were also passed through remnants of the ligaments and joint capsule, and all were fastened together . A sling was used for 3 weeks; then, full ROM exercise was allowed. At 3 months' follow-up, bony union of the left coracoid process was observed and the hook plate was removed. At 12 months' follow up, although a CT scan showed 2.5 mm residual superior displacement , it was not obvious on a physical examination. The patient did not have symptoms and completely returned to his previous work with full ROM.
3.759766
0.978516
sec[1]/sec[1]/p[1]
en
0.999997
29527368
https://doi.org/10.1155/2017/2935308
[ "clavicle", "reduction", "sutures", "injury", "hook", "plate", "clamp", "without", "passed", "full" ]
[ { "code": "LB72.Y", "title": "Other specified structural developmental anomalies of shoulder girdle" }, { "code": "FB86.11", "title": "Hypertrophy of bone" }, { "code": "ME85", "title": "Stiffness of joint" }, { "code": "FB80.Y", "title": "Other specified disorders of bone density or structure" }, { "code": "NC12.0Z", "title": "Fracture of clavicle, unspecified" }, { "code": "GC79", "title": "Disorders of breast reduction" }, { "code": "LB9A.Z", "title": "Reduction defects of lower limb, unspecified" }, { "code": "LB99.Z", "title": "Reduction defects of upper limb, unspecified" }, { "code": "LB9Z", "title": "Structural developmental anomalies of the skeleton, unspecified" }, { "code": "LB9A.Y", "title": "Other specified reduction defects of lower limb" } ]
=== ICD-11 CODES FOUND === [LB72.Y] Other specified structural developmental anomalies of shoulder girdle Also known as: Other specified structural developmental anomalies of shoulder girdle | Clavicular hypoplasia or aplasia | Absent clavicle | Medial condensing osteitis of clavicle | Congenital pseudoarthrosis of clavicle [FB86.11] Hypertrophy of bone Also known as: Hypertrophy of bone | bone thickening | periosteum thickening | Infantile cortical hyperostoses | Post traumatic subperiosteal ossification [ME85] Stiffness of joint Definition: Lack of range of motion of a joint secondary to pain, disease process or congenital malformation not detailed in or used in conjunction with other codes. Also known as: Stiffness of joint | joint stiffness | stiff joint | stiffness in joint | Stiffness of joint, multiple sites [FB80.Y] Other specified disorders of bone density or structure Also known as: Other specified disorders of bone density or structure | Bone dysplasia | Inherited bone dysplasia | Acquired bone dysplasia | Drug-induced bone dysplasia [NC12.0Z] Fracture of clavicle, unspecified Also known as: Fracture of clavicle, unspecified | Fracture of clavicle | fracture of collar bone | collar bone fracture dislocation [GC79] Disorders of breast reduction Also known as: Disorders of breast reduction [LB9A.Z] Reduction defects of lower limb, unspecified Also known as: Reduction defects of lower limb, unspecified | Reduction defects of lower limb | lower extremities underdeveloped [LB99.Z] Reduction defects of upper limb, unspecified Also known as: Reduction defects of upper limb, unspecified | Reduction defects of upper limb [LB9Z] Structural developmental anomalies of the skeleton, unspecified Also known as: Structural developmental anomalies of the skeleton, unspecified | Abnormal bone development | skeletal anomaly NOS [LB9A.Y] Other specified reduction defects of lower limb Also known as: Other specified reduction defects of lower limb === GRAPH WALKS === --- Walk 1 --- [LB72.Y] Other specified structural developmental anomalies of shoulder girdle --PARENT--> [LB72] Structural developmental anomalies of shoulder girdle Def: Any condition caused by failure of the shoulder girdle to correctly develop during the antenatal period.... --CHILD--> [LB72.1] Sprengel deformity Def: A condition caused by failure of the pectoral girdle to correctly develop during the antenatal period. This condition is characterised by abnormal descent, and altered position and anatomy of the scap... --- Walk 2 --- [LB72.Y] Other specified structural developmental anomalies of shoulder girdle --PARENT--> [LB72] Structural developmental anomalies of shoulder girdle Def: Any condition caused by failure of the shoulder girdle to correctly develop during the antenatal period.... --CHILD--> [LB72.2] Deformation of scapula --- Walk 3 --- [FB86.11] Hypertrophy of bone --PARENT--> [FB86.1] Bone hyperplasias --CHILD--> [FB86.11] Hypertrophy of bone --- Walk 4 --- [FB86.11] Hypertrophy of bone --PARENT--> [FB86.1] Bone hyperplasias --CHILD--> [FB86.1Y] Other specified bone hyperplasias --- Walk 5 --- [ME85] Stiffness of joint Def: Lack of range of motion of a joint secondary to pain, disease process or congenital malformation not detailed in or used in conjunction with other codes.... --PARENT--> [?] Symptoms or signs of the musculoskeletal system --RELATED_TO--> [?] Fear of musculoskeletal disease --- Walk 6 --- [ME85] Stiffness of joint Def: Lack of range of motion of a joint secondary to pain, disease process or congenital malformation not detailed in or used in conjunction with other codes.... --PARENT--> [?] Symptoms or signs of the musculoskeletal system --CHILD--> [ME81] Musculoskeletal chest pain
[ "[LB72.Y] Other specified structural developmental anomalies of shoulder girdle\n --PARENT--> [LB72] Structural developmental anomalies of shoulder girdle\n Def: Any condition caused by failure of the shoulder girdle to correctly develop during the antenatal period....\n --CHILD--> [LB72.1] Sprengel deformity\n Def: A condition caused by failure of the pectoral girdle to correctly develop during the antenatal period. This condition is characterised by abnormal descent, and altered position and anatomy of the scap...", "[LB72.Y] Other specified structural developmental anomalies of shoulder girdle\n --PARENT--> [LB72] Structural developmental anomalies of shoulder girdle\n Def: Any condition caused by failure of the shoulder girdle to correctly develop during the antenatal period....\n --CHILD--> [LB72.2] Deformation of scapula", "[FB86.11] Hypertrophy of bone\n --PARENT--> [FB86.1] Bone hyperplasias\n --CHILD--> [FB86.11] Hypertrophy of bone", "[FB86.11] Hypertrophy of bone\n --PARENT--> [FB86.1] Bone hyperplasias\n --CHILD--> [FB86.1Y] Other specified bone hyperplasias", "[ME85] Stiffness of joint\n Def: Lack of range of motion of a joint secondary to pain, disease process or congenital malformation not detailed in or used in conjunction with other codes....\n --PARENT--> [?] Symptoms or signs of the musculoskeletal system\n --RELATED_TO--> [?] Fear of musculoskeletal disease", "[ME85] Stiffness of joint\n Def: Lack of range of motion of a joint secondary to pain, disease process or congenital malformation not detailed in or used in conjunction with other codes....\n --PARENT--> [?] Symptoms or signs of the musculoskeletal system\n --CHILD--> [ME81] Musculoskeletal chest pain" ]
LB72.Y
Other specified structural developmental anomalies of shoulder girdle
[ { "from_icd11": "FB86.11", "icd10_code": "M89351", "icd10_title": "Hypertrophy of bone, right femur" }, { "from_icd11": "FB86.11", "icd10_code": "M89361", "icd10_title": "Hypertrophy of bone, right tibia" }, { "from_icd11": "FB86.11", "icd10_code": "M8938", "icd10_title": "Hypertrophy of bone, other site" }, { "from_icd11": "FB86.11", "icd10_code": "M89371", "icd10_title": "Hypertrophy of bone, right ankle and foot" }, { "from_icd11": "FB86.11", "icd10_code": "M89363", "icd10_title": "Hypertrophy of bone, right fibula" }, { "from_icd11": "FB86.11", "icd10_code": "M89333", "icd10_title": "Hypertrophy of bone, right radius" }, { "from_icd11": "FB86.11", "icd10_code": "M89362", "icd10_title": "Hypertrophy of bone, left tibia" }, { "from_icd11": "FB86.11", "icd10_code": "M8930", "icd10_title": "Hypertrophy of bone, unspecified site" }, { "from_icd11": "FB86.11", "icd10_code": "M893", "icd10_title": "Hypertrophy of bone" }, { "from_icd11": "ME85", "icd10_code": "M25661", "icd10_title": "Stiffness of right knee, not elsewhere classified" }, { "from_icd11": "ME85", "icd10_code": "M2560", "icd10_title": "Stiffness of unspecified joint, not elsewhere classified" }, { "from_icd11": "ME85", "icd10_code": "M25662", "icd10_title": "Stiffness of left knee, not elsewhere classified" }, { "from_icd11": "ME85", "icd10_code": "M25642", "icd10_title": "Stiffness of left hand, not elsewhere classified" }, { "from_icd11": "ME85", "icd10_code": "M25621", "icd10_title": "Stiffness of right elbow, not elsewhere classified" }, { "from_icd11": "ME85", "icd10_code": "M25612", "icd10_title": "Stiffness of left shoulder, not elsewhere classified" } ]
M89351
Hypertrophy of bone, right femur
To our knowledge this is the first description of the use of fibrin glue to cover the site of laser-excised tumor in the larynx in an attempt reduce the risk of postoperative bleeding, which is associated with significant morbidity and mortality. The senior author's involvement in an unpublished case of postoperative bleeding following laser resection of a supraglottic laryngeal tumor was instrumental in the adoption of the described technique. In that case, the patient developed chest pain and ECG signs of myocardial ischemia postoperatively resulting in the administration of anticoagulative therapy and, although the wound bed was dry immediately postoperatively, basal bronchopneumonia, respiratory failure, and death resulted from presumed slow laryngeal bleeding. This experience highlights the risk of an unprotected friable wound in the airway. Fibrin glue (fibrin sealant) is composed of human plasma proteins and mimics the final pathway of the coagulation cascade, yielding a stable and insoluble clot . The role of fibrin sealants throughout surgery is expanding and the use of fibrin has been described to line the repair of cricopharyngeal myotomy and in tracheal lacerations . Our patient suffered no complications associated with the use of fibrin glue and we have demonstrated that Tisseel can be applied to the larynx with the use of jet ventilation provided a pause in ventilation is permitted.
4.191406
0.765625
sec[2]/p[5]
en
0.999998
28154767
https://doi.org/10.1155/2017/2131068
[ "fibrin", "glue", "bleeding", "this", "laser", "tumor", "larynx", "risk", "postoperative", "associated" ]
[ { "code": "MC20.Y", "title": "Other specified clinical findings of the visual system" }, { "code": "BB20.Y", "title": "Other specified acute pericarditis" }, { "code": "DC50.Z", "title": "Peritonitis, unspecified" }, { "code": "3B2Y", "title": "Other specified haemorrhagic diseases due to acquired coagulation factor defects" }, { "code": "MD31", "title": "Pleurisy" }, { "code": "AA82", "title": "Chronic serous or mucoid otitis media" }, { "code": "6C4B.2Z", "title": "Volatile inhalant dependence, unspecified" }, { "code": "PB36", "title": "Unintentional exposure to or harmful effects of other or unspecified substances chiefly nonmedicinal as to source" }, { "code": "PD05", "title": "Intentional self-harm by exposure to or harmful effects of other or unspecified substances chiefly nonmedicinal as to source" }, { "code": "PH56", "title": "Exposure to or harmful effects of undetermined intent of other or unspecified substances chiefly nonmedicinal as to source" } ]
=== ICD-11 CODES FOUND === [MC20.Y] Other specified clinical findings of the visual system Also known as: Other specified clinical findings of the visual system | Fibrin in anterior chamber [BB20.Y] Other specified acute pericarditis Also known as: Other specified acute pericarditis | Acute nonspecific idiopathic pericarditis | acute nonspecific pericarditis | idiopathic pericarditis NOS | Pericarditis in vasculitis or connective tissue disease [DC50.Z] Peritonitis, unspecified Also known as: Peritonitis, unspecified | Peritonitis | peritoneum inflammation | peritonitis of undetermined cause | peritonitis of unspecified cause [3B2Y] Other specified haemorrhagic diseases due to acquired coagulation factor defects Also known as: Other specified haemorrhagic diseases due to acquired coagulation factor defects | Deficiency of coagulation factor due to vitamin K deficiency | Deficiency of coagulation factor due to nutritional vitamin K deficiency | Deficiency of coagulation factor due to other cause of vitamin K deficiency | Deficiency of coagulation factor due to other cause of vitamin K deficiency, coeliac disease included Includes: Deficiency of coagulation factor due to vitamin K deficiency | Acquired von Willebrand disease | Acquired prothrombin complex deficiency [MD31] Pleurisy Definition: Pleurisy or Pleuritis is the medical term for inflammation of the pleura. The most common cause of pleuritis is infection, but it can also be caused by lupus, rheumatoid arthritis, and certain medicines. Pleurisy or pleuritis usually accumulates exudative pleural effusions. Also known as: Pleurisy | pleuritis | pleurisy NOS | double pleurisy | pleurisy without effusion Excludes: pleurisy with effusion [AA82] Chronic serous or mucoid otitis media Definition: Chronic serous or mucoid otitis media is probably the most common form of sub-acute middle ear disease found in the developed world. It typically lingers following otitis media, when the fluid in the ear, formed by the infection, does not clear spontaneously. The tympanic membrane is intact but the middle ear is liquid- fluid filled. This presumably puts the middle ear at risk for further infection and often worsens hearing by about 30 dB. This is most frequently found in children and can interf Also known as: Chronic serous or mucoid otitis media | Chronic serous or mucoid otitis media with transudative | Chronic serous or mucoid otitis media with exudative | Chronic serous or mucoid otitis media with effusion | Seromucinous otitis media [6C4B.2Z] Volatile inhalant dependence, unspecified Also known as: Volatile inhalant dependence, unspecified | Volatile inhalant dependence | Volatile inhalant addiction | Glue sniffing dependence | glue sniffing addiction [PB36] Unintentional exposure to or harmful effects of other or unspecified substances chiefly nonmedicinal as to source Also known as: Unintentional exposure to or harmful effects of other or unspecified substances chiefly nonmedicinal as to source | Unintentional exposure to or harmful effects of other or unspecified gases, fumes or vapours | Unintentional exposure to or harmful effects of nitrogen oxides | Unintentional exposure to or harmful effects of sulfur dioxide | Unintentional exposure to or harmful effects of formaldehyde [PD05] Intentional self-harm by exposure to or harmful effects of other or unspecified substances chiefly nonmedicinal as to source Also known as: Intentional self-harm by exposure to or harmful effects of other or unspecified substances chiefly nonmedicinal as to source | intentional self-poisoning by exposure to or harmful effects of other and unspecified chemicals and noxious substances | intentional overdose of other and unspecified chemicals and noxious substances | Intentional self-harm by exposure to or harmful effects of other gases, fumes or vapours | Intentional self-harm by exposure to or harmful effects of nitrogen oxides [PH56] Exposure to or harmful effects of undetermined intent of other or unspecified substances chiefly nonmedicinal as to source Also known as: Exposure to or harmful effects of undetermined intent of other or unspecified substances chiefly nonmedicinal as to source | Exposure to or harmful effects of undetermined intent of other gases, fumes or vapours | Exposure to or harmful effects of undetermined intent of nitrogen oxides | Exposure to or harmful effects of undetermined intent of sulfur dioxide | Exposure to or harmful effects of undetermined intent of formaldehyde === GRAPH WALKS === --- Walk 1 --- [MC20.Y] Other specified clinical findings of the visual system --PARENT--> [MC20] Clinical findings of the visual system --CHILD--> [MC20.1] Small drusen of the macula --- Walk 2 --- [MC20.Y] Other specified clinical findings of the visual system --PARENT--> [MC20] Clinical findings of the visual system --CHILD--> [MC20.1] Small drusen of the macula --- Walk 3 --- [BB20.Y] Other specified acute pericarditis --PARENT--> [BB20] Acute pericarditis Def: Acute pericarditis is defined as pericardial inflammation of no more than 1 to 2 weeks duration.... --CHILD--> [BB20.0] Infectious pericarditis Def: A disease of the pericardium, caused by a secondary infection with a bacterial, viral, or fungal source. This disease is characterised by fever, odynophagia, cough, fatigue, or chest pain. Confirmatio... --- Walk 4 --- [BB20.Y] Other specified acute pericarditis --PARENT--> [BB20] Acute pericarditis Def: Acute pericarditis is defined as pericardial inflammation of no more than 1 to 2 weeks duration.... --EXCLUDES--> [?] Acute rheumatic pericarditis Def: A disease of the pericardium, caused by acute rheumatic fever. This disease is characterised by fever, dry cough, rapid heart rate, fatigue, or low blood pressure. Confirmation is by echocardiography,... --- Walk 5 --- [DC50.Z] Peritonitis, unspecified --PARENT--> [DC50] Peritonitis Def: Peritonitis is inflammation of the peritoneum, a condition marked by exudations in the peritoneum of serum, fibrin, cells, and pus.... --EXCLUDES--> [?] Puerperal sepsis --- Walk 6 --- [DC50.Z] Peritonitis, unspecified --PARENT--> [DC50] Peritonitis Def: Peritonitis is inflammation of the peritoneum, a condition marked by exudations in the peritoneum of serum, fibrin, cells, and pus.... --CHILD--> [DC50.0] Primary peritonitis Def: Peritonitis without surgical source nor the evident source of the infecting and other agent....
[ "[MC20.Y] Other specified clinical findings of the visual system\n --PARENT--> [MC20] Clinical findings of the visual system\n --CHILD--> [MC20.1] Small drusen of the macula", "[MC20.Y] Other specified clinical findings of the visual system\n --PARENT--> [MC20] Clinical findings of the visual system\n --CHILD--> [MC20.1] Small drusen of the macula", "[BB20.Y] Other specified acute pericarditis\n --PARENT--> [BB20] Acute pericarditis\n Def: Acute pericarditis is defined as pericardial inflammation of no more than 1 to 2 weeks duration....\n --CHILD--> [BB20.0] Infectious pericarditis\n Def: A disease of the pericardium, caused by a secondary infection with a bacterial, viral, or fungal source. This disease is characterised by fever, odynophagia, cough, fatigue, or chest pain. Confirmatio...", "[BB20.Y] Other specified acute pericarditis\n --PARENT--> [BB20] Acute pericarditis\n Def: Acute pericarditis is defined as pericardial inflammation of no more than 1 to 2 weeks duration....\n --EXCLUDES--> [?] Acute rheumatic pericarditis\n Def: A disease of the pericardium, caused by acute rheumatic fever. This disease is characterised by fever, dry cough, rapid heart rate, fatigue, or low blood pressure. Confirmation is by echocardiography,...", "[DC50.Z] Peritonitis, unspecified\n --PARENT--> [DC50] Peritonitis\n Def: Peritonitis is inflammation of the peritoneum, a condition marked by exudations in the peritoneum of serum, fibrin, cells, and pus....\n --EXCLUDES--> [?] Puerperal sepsis", "[DC50.Z] Peritonitis, unspecified\n --PARENT--> [DC50] Peritonitis\n Def: Peritonitis is inflammation of the peritoneum, a condition marked by exudations in the peritoneum of serum, fibrin, cells, and pus....\n --CHILD--> [DC50.0] Primary peritonitis\n Def: Peritonitis without surgical source nor the evident source of the infecting and other agent...." ]
MC20.Y
Other specified clinical findings of the visual system
[ { "from_icd11": "DC50.Z", "icd10_code": "K651", "icd10_title": "Peritoneal abscess" }, { "from_icd11": "DC50.Z", "icd10_code": "K652", "icd10_title": "Spontaneous bacterial peritonitis" }, { "from_icd11": "DC50.Z", "icd10_code": "K654", "icd10_title": "Sclerosing mesenteritis" }, { "from_icd11": "DC50.Z", "icd10_code": "K653", "icd10_title": "Choleperitonitis" }, { "from_icd11": "DC50.Z", "icd10_code": "K659", "icd10_title": "Peritonitis, unspecified" }, { "from_icd11": "DC50.Z", "icd10_code": "K658", "icd10_title": "Other peritonitis" }, { "from_icd11": "DC50.Z", "icd10_code": "K650", "icd10_title": "Generalized (acute) peritonitis" }, { "from_icd11": "DC50.Z", "icd10_code": "K65", "icd10_title": "Peritonitis" }, { "from_icd11": "MD31", "icd10_code": "R091", "icd10_title": "Pleurisy" }, { "from_icd11": "AA82", "icd10_code": "H6520", "icd10_title": "Chronic serous otitis media, unspecified ear" }, { "from_icd11": "AA82", "icd10_code": "H652", "icd10_title": "Chronic serous otitis media" }, { "from_icd11": "AA82", "icd10_code": "H653", "icd10_title": "Chronic mucoid otitis media" }, { "from_icd11": "6C4B.2Z", "icd10_code": "F18259", "icd10_title": "Inhalant dependence with inhalant-induced psychotic disorder, unspecified" }, { "from_icd11": "6C4B.2Z", "icd10_code": "F18280", "icd10_title": "Inhalant dependence with inhalant-induced anxiety disorder" }, { "from_icd11": "6C4B.2Z", "icd10_code": "F18288", "icd10_title": "Inhalant dependence with other inhalant-induced disorder" } ]
K651
Peritoneal abscess
A high degree of clinical suspicion is required for an early and correct diagnosis in the absence of an odontogenic etiology . Comprehensive history taking and intraoral examination complete with pulp viability testing and dental X-rays are usually sufficient for a diagnosis . Cone beam CT is unmatched when plane radiography is equivocal or inefficient in determining the extent and the relations of the periapical lesion with the adjacent teeth . Fistulography via X-ray or CT using a gutta-percha usually provides the diagnosis when all other modalities fail . Several authors describe treatment as removing the original source of infection by means of endodontic or extraction therapy with spontaneous closure of the fistulous tract within as much as 2 weeks . Notably, surgical revision or fistulectomy is usually reserved for those cases whose fistulous tracts fail to terminate and those patients with aesthetically unpleasant hyperpigmented scared tissue . In this case, the fistula's aperture seemed to be in close proximity to the distribution of marginal mandibular branch of the facial nerve. As such, a preliminary superficial parotidectomy with wide exposure was adopted to aid in identification and preservation of the branches of the facial nerve. Once the facial nerve branches were identified, an elliptical incision was made around the fistulas opening and the fistulous tract meticulously stripped.
4.183594
0.57959
sec[2]/p[1]
en
0.999998
29991948
https://doi.org/10.1155/2018/3710857
[ "usually", "fistulous", "facial", "nerve", "fail", "tract", "those", "branches", "degree", "suspicion" ]
[ { "code": "LA8Y", "title": "Other specified structural developmental anomaly of heart or great vessels" }, { "code": "2E67.13", "title": "High grade squamous intraepithelial lesion of vulva, HPV-associated" }, { "code": "ED90.1", "title": "Periorificial dermatitis" }, { "code": "8B88.0", "title": "Bell palsy" }, { "code": "LA51", "title": "Facial clefts" }, { "code": "8B88.Z", "title": "Disorders of facial nerve, unspecified" }, { "code": "LA52", "title": "Facial asymmetry" }, { "code": "8C1Z", "title": "Mononeuropathy of unspecified site" }, { "code": "ND56.4", "title": "Injury of nerve of unspecified body region" }, { "code": "8B80", "title": "Disorders of olfactory nerve" } ]
=== ICD-11 CODES FOUND === [LA8Y] Other specified structural developmental anomaly of heart or great vessels Also known as: Other specified structural developmental anomaly of heart or great vessels | Congenital anomaly of position or spatial relationships of thoraco-abdominal organs | Usual atrial arrangement | atrial situs solitus | Abnormal atrial arrangement [2E67.13] High grade squamous intraepithelial lesion of vulva, HPV-associated Definition: Squamous intraepithelial lesions (SILs) of the vulva (also known as vulvar intraepithelial neoplasia [VIN]), HPV-associated, are proliferations of squamous cells driven by HPV infection, showing maturation abnormalities and nuclear hyperchromasia that do not extend beyond the basement membrane. Also known as: High grade squamous intraepithelial lesion of vulva, HPV-associated | Vulvar intraepithelial neoplasia, usual type | Vulvar intraepithelial neoplasia, usual (classical) | VIN III, HPV associated | VIN II, HPV associated [ED90.1] Periorificial dermatitis Definition: Periorificial dermatitis is a term which links two erythematous and papulopustular facial dermatoses that are strongly linked to prolonged potent topical corticosteroid use, namely perioral dermatitis and periocular dermatitis. It is characterised by the development of erythema, papules and pustules in perioral and periocular skin. Also known as: Periorificial dermatitis | Perioral dermatitis | Corticosteroid-induced perioral dermatitis | Periocular dermatitis | Periorificial dermatitis of eyelids [8B88.0] Bell palsy Also known as: Bell palsy | Facial nerve paralysis | Facial nerve palsy | Seventh cranial nerve paralysis | facial palsy [LA51] Facial clefts Definition: Any condition caused by failure of the structures of the face to correctly develop during the antenatal period. These conditions are characterised by a partition in bone, soft tissue, or skin of the face. Also known as: Facial clefts | Craniofacial clefts | Median facial cleft | Tessier number 0-14 and 30 facial cleft | Midline facial cleft Excludes: Frontofacionasal dysostosis | Frontonasal dysplasia [8B88.Z] Disorders of facial nerve, unspecified Also known as: Disorders of facial nerve, unspecified | Disorders of facial nerve | Neuropathy of facial nerve | Disorders of 7th cranial nerve | Disorders of the seventh cranial nerve [LA52] Facial asymmetry Definition: A condition caused by failure of the face to develop symmetrically during the antenatal period. Also known as: Facial asymmetry | Asymmetric face | Hemifacial atrophy | Facial hemiatrophy | Hemifacial hypertrophy [8C1Z] Mononeuropathy of unspecified site Also known as: Mononeuropathy of unspecified site | inflammation of nerve NOS | nerve condition NOS | neuritis NOS | nerve disease NOS [ND56.4] Injury of nerve of unspecified body region Also known as: Injury of nerve of unspecified body region | injuries to nerves, nerve plexuses and roots | injury to nerves, unspecified site | nerve damage NOS | Injury of nerve NOS Excludes: multiple injuries of nerves NOS [8B80] Disorders of olfactory nerve Also known as: Disorders of olfactory nerve | disorders of olfactory [1st] nerve | disorders of the first nerve | first cranial nerve disorder | disease of first cranial nerve Includes: Disorder of 1st cranial nerve Excludes: Idiopathic anosmia | Idiopathic parosmia === GRAPH WALKS === --- Walk 1 --- [LA8Y] Other specified structural developmental anomaly of heart or great vessels --PARENT--> [?] Structural developmental anomaly of heart or great vessels Def: A congenital malformation of the heart and/or great vessels or an acquired abnormality unique to the congenitally malformed heart.... --RELATED_TO--> [?] Congenital great vessel related acquired abnormality Def: Any postnatal pathological change in form or function of the heart and/or great vessels consequent to the presence of congenital cardiovascular disease.... --- Walk 2 --- [LA8Y] Other specified structural developmental anomaly of heart or great vessels --PARENT--> [?] Structural developmental anomaly of heart or great vessels Def: A congenital malformation of the heart and/or great vessels or an acquired abnormality unique to the congenitally malformed heart.... --RELATED_TO--> [?] Congenital cardiac tumor, not otherwise specified Def: A congenital malformation consisting of growth of abnormal tissue within the heart.... --- Walk 3 --- [2E67.13] High grade squamous intraepithelial lesion of vulva, HPV-associated Def: Squamous intraepithelial lesions (SILs) of the vulva (also known as vulvar intraepithelial neoplasia [VIN]), HPV-associated, are proliferations of squamous cells driven by HPV infection, showing matur... --PARENT--> [2E67.1] Carcinoma in situ of vulva --EXCLUDES--> [?] Low grade squamous intraepithelial lesion of vulva Def: A condition of the vulva, characterised by lesion of the squamous vulvar intraepithelial cells, leading to unspecified grade or severity of dysplasia and varying degrees of atypia of the cells. This c... --- Walk 4 --- [2E67.13] High grade squamous intraepithelial lesion of vulva, HPV-associated Def: Squamous intraepithelial lesions (SILs) of the vulva (also known as vulvar intraepithelial neoplasia [VIN]), HPV-associated, are proliferations of squamous cells driven by HPV infection, showing matur... --RELATED_TO--> [?] Bowenoid papulosis of the vulva --PARENT--> [?] Genital warts of vulva Def: Human papillomavirus (HPV) infection of vulval skin. Vulval warts are usually transmitted by sexual contact. On the vulva they may appear as flat moist papules and plaques on the labia or as cauliflow... --- Walk 5 --- [ED90.1] Periorificial dermatitis Def: Periorificial dermatitis is a term which links two erythematous and papulopustular facial dermatoses that are strongly linked to prolonged potent topical corticosteroid use, namely perioral dermatitis... --PARENT--> [ED90] Rosacea and related disorders --CHILD--> [ED90.0] Rosacea Def: The term rosacea encompasses a spectrum of changes that occur mainly in facial skin but may also involve the eyes. Most patients with rosacea have facial erythema and vascular instability which are va... --- Walk 6 --- [ED90.1] Periorificial dermatitis Def: Periorificial dermatitis is a term which links two erythematous and papulopustular facial dermatoses that are strongly linked to prolonged potent topical corticosteroid use, namely perioral dermatitis... --PARENT--> [ED90] Rosacea and related disorders --CHILD--> [ED90.1] Periorificial dermatitis Def: Periorificial dermatitis is a term which links two erythematous and papulopustular facial dermatoses that are strongly linked to prolonged potent topical corticosteroid use, namely perioral dermatitis...
[ "[LA8Y] Other specified structural developmental anomaly of heart or great vessels\n --PARENT--> [?] Structural developmental anomaly of heart or great vessels\n Def: A congenital malformation of the heart and/or great vessels or an acquired abnormality unique to the congenitally malformed heart....\n --RELATED_TO--> [?] Congenital great vessel related acquired abnormality\n Def: Any postnatal pathological change in form or function of the heart and/or great vessels consequent to the presence of congenital cardiovascular disease....", "[LA8Y] Other specified structural developmental anomaly of heart or great vessels\n --PARENT--> [?] Structural developmental anomaly of heart or great vessels\n Def: A congenital malformation of the heart and/or great vessels or an acquired abnormality unique to the congenitally malformed heart....\n --RELATED_TO--> [?] Congenital cardiac tumor, not otherwise specified\n Def: A congenital malformation consisting of growth of abnormal tissue within the heart....", "[2E67.13] High grade squamous intraepithelial lesion of vulva, HPV-associated\n Def: Squamous intraepithelial lesions (SILs) of the vulva (also known as vulvar intraepithelial neoplasia [VIN]), HPV-associated, are proliferations of squamous cells driven by HPV infection, showing matur...\n --PARENT--> [2E67.1] Carcinoma in situ of vulva\n --EXCLUDES--> [?] Low grade squamous intraepithelial lesion of vulva\n Def: A condition of the vulva, characterised by lesion of the squamous vulvar intraepithelial cells, leading to unspecified grade or severity of dysplasia and varying degrees of atypia of the cells. This c...", "[2E67.13] High grade squamous intraepithelial lesion of vulva, HPV-associated\n Def: Squamous intraepithelial lesions (SILs) of the vulva (also known as vulvar intraepithelial neoplasia [VIN]), HPV-associated, are proliferations of squamous cells driven by HPV infection, showing matur...\n --RELATED_TO--> [?] Bowenoid papulosis of the vulva\n --PARENT--> [?] Genital warts of vulva\n Def: Human papillomavirus (HPV) infection of vulval skin. Vulval warts are usually transmitted by sexual contact. On the vulva they may appear as flat moist papules and plaques on the labia or as cauliflow...", "[ED90.1] Periorificial dermatitis\n Def: Periorificial dermatitis is a term which links two erythematous and papulopustular facial dermatoses that are strongly linked to prolonged potent topical corticosteroid use, namely perioral dermatitis...\n --PARENT--> [ED90] Rosacea and related disorders\n --CHILD--> [ED90.0] Rosacea\n Def: The term rosacea encompasses a spectrum of changes that occur mainly in facial skin but may also involve the eyes. Most patients with rosacea have facial erythema and vascular instability which are va...", "[ED90.1] Periorificial dermatitis\n Def: Periorificial dermatitis is a term which links two erythematous and papulopustular facial dermatoses that are strongly linked to prolonged potent topical corticosteroid use, namely perioral dermatitis...\n --PARENT--> [ED90] Rosacea and related disorders\n --CHILD--> [ED90.1] Periorificial dermatitis\n Def: Periorificial dermatitis is a term which links two erythematous and papulopustular facial dermatoses that are strongly linked to prolonged potent topical corticosteroid use, namely perioral dermatitis..." ]
LA8Y
Other specified structural developmental anomaly of heart or great vessels
[ { "from_icd11": "LA8Y", "icd10_code": "Q248 ", "icd10_title": "" }, { "from_icd11": "ED90.1", "icd10_code": "L710", "icd10_title": "Perioral dermatitis" }, { "from_icd11": "8B88.0", "icd10_code": "G510", "icd10_title": "Bell's palsy" }, { "from_icd11": "LA51", "icd10_code": "Q361", "icd10_title": "Cleft lip, median" }, { "from_icd11": "8B88.Z", "icd10_code": "G512", "icd10_title": "Melkersson's syndrome" }, { "from_icd11": "8B88.Z", "icd10_code": "G518", "icd10_title": "Other disorders of facial nerve" }, { "from_icd11": "8B88.Z", "icd10_code": "G519", "icd10_title": "Disorder of facial nerve, unspecified" }, { "from_icd11": "8B88.Z", "icd10_code": "G51", "icd10_title": "Facial nerve disorders" }, { "from_icd11": "8B88.Z", "icd10_code": "G511", "icd10_title": "Geniculate ganglionitis" }, { "from_icd11": "8B88.Z", "icd10_code": "G836", "icd10_title": "" }, { "from_icd11": "LA52", "icd10_code": "Q670", "icd10_title": "Congenital facial asymmetry" }, { "from_icd11": "8C1Z", "icd10_code": "G59", "icd10_title": "Mononeuropathy in diseases classified elsewhere" }, { "from_icd11": "8C1Z", "icd10_code": "G598", "icd10_title": "" }, { "from_icd11": "ND56.4", "icd10_code": "T144", "icd10_title": "" }, { "from_icd11": "8B80", "icd10_code": "G520", "icd10_title": "Disorders of olfactory nerve" } ]
Q248
To make matters worse, this issue has received insufficient attention. Promotion of modern diagnostic technology, a lack of bedside teaching, and decreased interest in physical examination owing to time limitations has led to the further neglect of physical examination competence . Our case aims to raise awareness of this decay in clinical skills and its probable negative impact on patient outcomes. For instance, our patient was originally diagnosed with Bell’s palsy. Classically, Bell’s palsy causes weakness of the entire unilateral face, including the failure of forehead muscle wrinkling on the affected side. However, in actuality, there was sparing of the forehead muscles on the affected side in our patient, owing to the bilateral innervation of these muscles. This generally should have prompted suspicion of a central nervous system lesion, such as stroke. The resulting delay in diagnosis contributed to patient morbidity, an unfortunate consequence that could have been avoided with a good physical exam. A thorough physical examination itself is certainly not a substitute for the use of technology. However, we encourage the appropriate application of a thorough history and physical examination to guide the prudent use of technology. Potential advantages of this approach include enhanced physician-patient relationship, improved patient safety, fewer diagnostic errors, and lower financial costs .
4.070313
0.912598
sec[2]/p[1]
en
0.999998
28589061
https://doi.org/10.7759/cureus.1212
[ "physical", "this", "technology", "owing", "bell", "palsy", "forehead", "affected", "side", "however" ]
[ { "code": "MG44.1Z", "title": "Lack of expected normal physiological development, unspecified" }, { "code": "PJ20", "title": "Physical maltreatment" }, { "code": "MB23.0", "title": "Aggressive behaviour" }, { "code": "QD70.Z", "title": "Problems associated with the natural environment or human-made changes to the environment, unspecified" }, { "code": "QE82.0", "title": "Personal history of physical abuse" }, { "code": "4A01.03", "title": "Transient hypogammaglobulinaemia of infancy" }, { "code": "QA30.1Z", "title": "Contact with health services for unspecified assisted reproductive technology" }, { "code": "QA30.1Y", "title": "Contact with health services for other specified assisted reproductive technology" }, { "code": "QA30.20", "title": "Contact with health services for controlled ovarian stimulation for assisted reproductive technology" }, { "code": "QA30.21", "title": "Contact with health services for controlled ovarian stimulation for non-assisted reproductive technology cycles" } ]
=== ICD-11 CODES FOUND === [MG44.1Z] Lack of expected normal physiological development, unspecified Also known as: Lack of expected normal physiological development, unspecified | Lack of expected normal physiological development | delayed physiological development | unspecified delay in development | development arrest [PJ20] Physical maltreatment Definition: Non-accidental acts of physical force that result, or have reasonable potential to result, in physical harm or that evoke significant fear. The category is applied to the victim of the maltreatment, not the perpetrator. Also known as: Physical maltreatment | physical abuse | Shaken infant syndrome | shaken baby syndrome | Battered baby syndrome [MB23.0] Aggressive behaviour Definition: Actions intended to threaten or hurt another person or to damage property that may be physical, verbal, or symbolic (e.g., acting against the other person's interests). Aggressive behaviour may be appropriate and self-protective, or inappropriate, hostile, and destructive. Also known as: Aggressive behaviour | Violent behaviour | physical violence [QD70.Z] Problems associated with the natural environment or human-made changes to the environment, unspecified Also known as: Problems associated with the natural environment or human-made changes to the environment, unspecified | Problems associated with the natural environment or human-made changes to the environment | physical environment problem | exposure to pollution NOS | unsatisfactory physical environment [QE82.0] Personal history of physical abuse Definition: Personal history of non-accidental acts of physical force that result, or have reasonable potential to result, in physical harm or that evoke significant fear. This category is applied to the victim of the maltreatment, not the perpetrator. Also known as: Personal history of physical abuse | Personal history of physical maltreatment | Physical abuse of child Excludes: History of spouse or partner violence, physical [4A01.03] Transient hypogammaglobulinaemia of infancy Also known as: Transient hypogammaglobulinaemia of infancy | immunoglobulin maturational delay | THI - [transient hypogammaglobulinaemia of infancy] [QA30.1Z] Contact with health services for unspecified assisted reproductive technology Also known as: Contact with health services for unspecified assisted reproductive technology | Contact with health services for assisted reproductive technology | ART - [assisted reproductive technology] [QA30.1Y] Contact with health services for other specified assisted reproductive technology Also known as: Contact with health services for other specified assisted reproductive technology [QA30.20] Contact with health services for controlled ovarian stimulation for assisted reproductive technology Definition: Medical treatment in which women are stimulated to induce the development of multiple ovarian follicles to obtain multiple oocytes at follicular aspiration. Also known as: Contact with health services for controlled ovarian stimulation for assisted reproductive technology | COS - [controlled ovarian stimulation] for ART - [assisted reproductive technology] [QA30.21] Contact with health services for controlled ovarian stimulation for non-assisted reproductive technology cycles Definition: Pharmacological treatment for women with normal ovulatory cycles in which the ovaries are stimulated to ovulate more than one oocyte. Also known as: Contact with health services for controlled ovarian stimulation for non-assisted reproductive technology cycles | COS - [controlled ovarian stimulation] for non-ART - [non-assisted reproductive technology] cycles === GRAPH WALKS === --- Walk 1 --- [MG44.1Z] Lack of expected normal physiological development, unspecified --PARENT--> [MG44.1] Lack of expected normal physiological development Def: Lack of expected normal physiological development includes delayed milestone of development and other lack of expected normal physiological development including gross and fine motor development, lang... --CHILD--> [MG44.11] Failure to thrive in infant or child Def: When an infant or child's current weight or rate of weight gain is significantly below that of other children of similar age and gender.... --- Walk 2 --- [MG44.1Z] Lack of expected normal physiological development, unspecified --PARENT--> [MG44.1] Lack of expected normal physiological development Def: Lack of expected normal physiological development includes delayed milestone of development and other lack of expected normal physiological development including gross and fine motor development, lang... --CHILD--> [MG44.12] Short stature of child Def: Short stature is when a child is significantly shorter than children of the same age and gender... --- Walk 3 --- [PJ20] Physical maltreatment Def: Non-accidental acts of physical force that result, or have reasonable potential to result, in physical harm or that evoke significant fear. The category is applied to the victim of the maltreatment, n... --PARENT--> [?] Maltreatment Def: Non-accidental acts of physical force, forced or coerced sexual acts, verbal or symbolic acts, or significant caregiving omissions that result in harm or have a reasonable potential for harm. These ca... --CHILD--> [PJ20] Physical maltreatment Def: Non-accidental acts of physical force that result, or have reasonable potential to result, in physical harm or that evoke significant fear. The category is applied to the victim of the maltreatment, n... --- Walk 4 --- [PJ20] Physical maltreatment Def: Non-accidental acts of physical force that result, or have reasonable potential to result, in physical harm or that evoke significant fear. The category is applied to the victim of the maltreatment, n... --PARENT--> [?] Maltreatment Def: Non-accidental acts of physical force, forced or coerced sexual acts, verbal or symbolic acts, or significant caregiving omissions that result in harm or have a reasonable potential for harm. These ca... --CHILD--> [PJ22] Psychological maltreatment Def: Non-accidental verbal or symbolic acts that result in significant psychological harm. The category is applied to the victim of the maltreatment, not the perpetrator.... --- Walk 5 --- [MB23.0] Aggressive behaviour Def: Actions intended to threaten or hurt another person or to damage property that may be physical, verbal, or symbolic (e.g., acting against the other person's interests). Aggressive behaviour may be app... --PARENT--> [MB23] Symptoms or signs involving appearance or behaviour --RELATED_TO--> [?] Speech dysfluency Def: Speech dysfluency is characterised by the frequent or pervasive disruption of the rhythmic flow of speech that arises subsequent to the developmental period (i.e., adult onset) and is outside the limi... --- Walk 6 --- [MB23.0] Aggressive behaviour Def: Actions intended to threaten or hurt another person or to damage property that may be physical, verbal, or symbolic (e.g., acting against the other person's interests). Aggressive behaviour may be app... --PARENT--> [MB23] Symptoms or signs involving appearance or behaviour --CHILD--> [MB23.1] Antisocial behaviour Def: Behaviour in which the basic rights of others or major age-appropriate societal norms, rules, or laws, are violated....
[ "[MG44.1Z] Lack of expected normal physiological development, unspecified\n --PARENT--> [MG44.1] Lack of expected normal physiological development\n Def: Lack of expected normal physiological development includes delayed milestone of development and other lack of expected normal physiological development including gross and fine motor development, lang...\n --CHILD--> [MG44.11] Failure to thrive in infant or child\n Def: When an infant or child's current weight or rate of weight gain is significantly below that of other children of similar age and gender....", "[MG44.1Z] Lack of expected normal physiological development, unspecified\n --PARENT--> [MG44.1] Lack of expected normal physiological development\n Def: Lack of expected normal physiological development includes delayed milestone of development and other lack of expected normal physiological development including gross and fine motor development, lang...\n --CHILD--> [MG44.12] Short stature of child\n Def: Short stature is when a child is significantly shorter than children of the same age and gender...", "[PJ20] Physical maltreatment\n Def: Non-accidental acts of physical force that result, or have reasonable potential to result, in physical harm or that evoke significant fear. The category is applied to the victim of the maltreatment, n...\n --PARENT--> [?] Maltreatment\n Def: Non-accidental acts of physical force, forced or coerced sexual acts, verbal or symbolic acts, or significant caregiving omissions that result in harm or have a reasonable potential for harm. These ca...\n --CHILD--> [PJ20] Physical maltreatment\n Def: Non-accidental acts of physical force that result, or have reasonable potential to result, in physical harm or that evoke significant fear. The category is applied to the victim of the maltreatment, n...", "[PJ20] Physical maltreatment\n Def: Non-accidental acts of physical force that result, or have reasonable potential to result, in physical harm or that evoke significant fear. The category is applied to the victim of the maltreatment, n...\n --PARENT--> [?] Maltreatment\n Def: Non-accidental acts of physical force, forced or coerced sexual acts, verbal or symbolic acts, or significant caregiving omissions that result in harm or have a reasonable potential for harm. These ca...\n --CHILD--> [PJ22] Psychological maltreatment\n Def: Non-accidental verbal or symbolic acts that result in significant psychological harm. The category is applied to the victim of the maltreatment, not the perpetrator....", "[MB23.0] Aggressive behaviour\n Def: Actions intended to threaten or hurt another person or to damage property that may be physical, verbal, or symbolic (e.g., acting against the other person's interests). Aggressive behaviour may be app...\n --PARENT--> [MB23] Symptoms or signs involving appearance or behaviour\n --RELATED_TO--> [?] Speech dysfluency\n Def: Speech dysfluency is characterised by the frequent or pervasive disruption of the rhythmic flow of speech that arises subsequent to the developmental period (i.e., adult onset) and is outside the limi...", "[MB23.0] Aggressive behaviour\n Def: Actions intended to threaten or hurt another person or to damage property that may be physical, verbal, or symbolic (e.g., acting against the other person's interests). Aggressive behaviour may be app...\n --PARENT--> [MB23] Symptoms or signs involving appearance or behaviour\n --CHILD--> [MB23.1] Antisocial behaviour\n Def: Behaviour in which the basic rights of others or major age-appropriate societal norms, rules, or laws, are violated...." ]
MG44.1Z
Lack of expected normal physiological development, unspecified
[ { "from_icd11": "MG44.1Z", "icd10_code": "R6250", "icd10_title": "Unspecified lack of expected normal physiological development in childhood" }, { "from_icd11": "MG44.1Z", "icd10_code": "R6259", "icd10_title": "Other lack of expected normal physiological development in childhood" }, { "from_icd11": "MG44.1Z", "icd10_code": "R6251", "icd10_title": "Failure to thrive (child)" }, { "from_icd11": "MG44.1Z", "icd10_code": "R6252", "icd10_title": "Short stature (child)" }, { "from_icd11": "MG44.1Z", "icd10_code": "R62", "icd10_title": "Lack of expected normal physiological development in childhood and adults" }, { "from_icd11": "MG44.1Z", "icd10_code": "R628", "icd10_title": "" }, { "from_icd11": "MG44.1Z", "icd10_code": "R629", "icd10_title": "" }, { "from_icd11": "PJ20", "icd10_code": "T7411XA", "icd10_title": "Adult physical abuse, confirmed, initial encounter" }, { "from_icd11": "PJ20", "icd10_code": "T7411XS", "icd10_title": "Adult physical abuse, confirmed, sequela" }, { "from_icd11": "PJ20", "icd10_code": "T741", "icd10_title": "Physical abuse, confirmed" }, { "from_icd11": "PJ20", "icd10_code": "Y06", "icd10_title": "" }, { "from_icd11": "MB23.0", "icd10_code": "R456", "icd10_title": "Violent behavior" }, { "from_icd11": "QD70.Z", "icd10_code": "Z58", "icd10_title": "" }, { "from_icd11": "QD70.Z", "icd10_code": "Z585", "icd10_title": "" }, { "from_icd11": "QD70.Z", "icd10_code": "Z588", "icd10_title": "" } ]
R6250
Unspecified lack of expected normal physiological development in childhood
The patient’s complete blood count showed a total white blood cell (WBC) count of 6.6 × 10 9 /L (60% neutrophils, 15% lymphocytes, and 25% monocytes), hemoglobin of 9.1 g/dl, and a platelet count of 36 × 10 9 /L. A peripheral smear taken upon admission showed normochromic normocytic anemia with marked monocytosis and apparently low platelets that could have been due to multiple platelet clumps, and there was no evidence of microangiopathic hemolytic anemia (MAHA), but subsequent peripheral smears drawn on the third and fifth days of admission showed evidence of MAHA with marked thrombocytopenia. The patient’s prothrombin time was 15.7 s (control 12 s), and her activated partial thromboplastin time was 36 s (control 25 s). Her d -dimer level was 1500 ng/ml (normal range < 500 ng/ml). Her fibrinogen levels were not available in the hospital. Her transaminases were within the normal ranges. Her serum protein concentration was 61 g/L with albumin of 30 g/L. The results of her renal function tests were normal. Her serum lactate dehydrogenase was 810 U/L (normal range 225–450 U/L). The results of her blood and urine cultures were sterile. A transthoracic echocardiogram showed normal cardiac valves and endocardium. The result of immunofluorescence antibody testing of rickettsial immunoglobulin G was strongly positive for Rickettsia conorii , with a rise in titer convalescent sera repeated after 2 weeks.
4.089844
0.968262
sec[1]/p[1]
en
0.999998
29801512
https://doi.org/10.1186/s13256-018-1672-5
[ "blood", "count", "platelet", "anemia", "evidence", "maha", "time", "control", "range", "serum" ]
[ { "code": "3C0Z", "title": "Diseases of the blood or blood-forming organs, unspecified" }, { "code": "MF50.4Z", "title": "Haematuria, unspecified" }, { "code": "MA12.1", "title": "Finding of cocaine in blood" }, { "code": "MA12.4", "title": "Finding of steroid agent in blood" }, { "code": "MA12.2", "title": "Finding of hallucinogen in blood" }, { "code": "3B63.1Z", "title": "Acquired thrombocytosis, unspecified" }, { "code": "3B64.Z", "title": "Thrombocytopenia, unspecified" }, { "code": "4B0Z", "title": "Immune system disorders involving white cell lineages, unspecified" }, { "code": "4B03.Z", "title": "Eosinophilia, unspecified" }, { "code": "4B00.1Z", "title": "Neutrophilia, unspecified" } ]
=== ICD-11 CODES FOUND === [3C0Z] Diseases of the blood or blood-forming organs, unspecified Also known as: Diseases of the blood or blood-forming organs, unspecified | Blood, lymph or spleen disease | blood condition NOS | blood disorder NOS | bone marrow disease NOS [MF50.4Z] Haematuria, unspecified Also known as: Haematuria, unspecified | Haematuria | blood in urine | urinary blood | haematuria NOS [MA12.1] Finding of cocaine in blood Also known as: Finding of cocaine in blood | cocaine in blood [MA12.4] Finding of steroid agent in blood Also known as: Finding of steroid agent in blood | steroid in blood [MA12.2] Finding of hallucinogen in blood Also known as: Finding of hallucinogen in blood | hallucinogen in blood [3B63.1Z] Acquired thrombocytosis, unspecified Also known as: Acquired thrombocytosis, unspecified | Acquired thrombocytosis | Idiopathic haemorrhagic thrombocythaemia | Essential thrombocythaemia | primary haemorrhagic thrombocythaemia [3B64.Z] Thrombocytopenia, unspecified Also known as: Thrombocytopenia, unspecified | Thrombocytopenia | low platelet count | low platelets | decreased platelets [4B0Z] Immune system disorders involving white cell lineages, unspecified Also known as: Immune system disorders involving white cell lineages, unspecified [4B03.Z] Eosinophilia, unspecified Also known as: Eosinophilia, unspecified | Eosinophilia | Disorders with increased eosinophil counts | Idiopathic hypereosinophilic syndrome [4B00.1Z] Neutrophilia, unspecified Also known as: Neutrophilia, unspecified | Neutrophilia | Disorders with increased neutrophil counts === GRAPH WALKS === --- Walk 1 --- [3C0Z] Diseases of the blood or blood-forming organs, unspecified --PARENT--> [03] Diseases of the blood or blood-forming organs Def: This chapter includes diseases of the blood as well as diseases of blood forming organs.... --EXCLUDES--> [?] Pregnancy, childbirth or the puerperium Def: A group of conditions characterised as occurring during the period of time from conception to delivery (pregnancy), during labour and delivery (childbirth) or during the approximately six weeks after ... --- Walk 2 --- [3C0Z] Diseases of the blood or blood-forming organs, unspecified --PARENT--> [03] Diseases of the blood or blood-forming organs Def: This chapter includes diseases of the blood as well as diseases of blood forming organs.... --RELATED_TO--> [?] Symptoms, signs or clinical findings of blood, blood-forming organs, or the immune system --- Walk 3 --- [MF50.4Z] Haematuria, unspecified --PARENT--> [MF50.4] Haematuria Def: Hematuria means presence of blood or red blood cells (RBCs) in the urine. There are two types of hematuria: gross hematuria (when one can see the blood in the urine) and microscopic hematuria (when th... --CHILD--> [MF50.41] Microscopic haematuria --- Walk 4 --- [MF50.4Z] Haematuria, unspecified --PARENT--> [MF50.4] Haematuria Def: Hematuria means presence of blood or red blood cells (RBCs) in the urine. There are two types of hematuria: gross hematuria (when one can see the blood in the urine) and microscopic hematuria (when th... --EXCLUDES--> [?] Recurrent or persistent glomerular haematuria Def: The presence in the urine of glomerular origin red blood cells (RBCs). In microscopic haematuria the urine appears normal to the naked eye, but examination with a microscope shows a high number of RBC... --- Walk 5 --- [MA12.1] Finding of cocaine in blood --PARENT--> [MA12] Clinical findings of drugs, medicaments and biological substances in blood, blood-forming organs, or the immune system --CHILD--> [MA12.2] Finding of hallucinogen in blood --- Walk 6 --- [MA12.1] Finding of cocaine in blood --PARENT--> [MA12] Clinical findings of drugs, medicaments and biological substances in blood, blood-forming organs, or the immune system --CHILD--> [MA12.0] Finding of opiate drug in blood
[ "[3C0Z] Diseases of the blood or blood-forming organs, unspecified\n --PARENT--> [03] Diseases of the blood or blood-forming organs\n Def: This chapter includes diseases of the blood as well as diseases of blood forming organs....\n --EXCLUDES--> [?] Pregnancy, childbirth or the puerperium\n Def: A group of conditions characterised as occurring during the period of time from conception to delivery (pregnancy), during labour and delivery (childbirth) or during the approximately six weeks after ...", "[3C0Z] Diseases of the blood or blood-forming organs, unspecified\n --PARENT--> [03] Diseases of the blood or blood-forming organs\n Def: This chapter includes diseases of the blood as well as diseases of blood forming organs....\n --RELATED_TO--> [?] Symptoms, signs or clinical findings of blood, blood-forming organs, or the immune system", "[MF50.4Z] Haematuria, unspecified\n --PARENT--> [MF50.4] Haematuria\n Def: Hematuria means presence of blood or red blood cells (RBCs) in the urine. There are two types of hematuria: gross hematuria (when one can see the blood in the urine) and microscopic hematuria (when th...\n --CHILD--> [MF50.41] Microscopic haematuria", "[MF50.4Z] Haematuria, unspecified\n --PARENT--> [MF50.4] Haematuria\n Def: Hematuria means presence of blood or red blood cells (RBCs) in the urine. There are two types of hematuria: gross hematuria (when one can see the blood in the urine) and microscopic hematuria (when th...\n --EXCLUDES--> [?] Recurrent or persistent glomerular haematuria\n Def: The presence in the urine of glomerular origin red blood cells (RBCs). In microscopic haematuria the urine appears normal to the naked eye, but examination with a microscope shows a high number of RBC...", "[MA12.1] Finding of cocaine in blood\n --PARENT--> [MA12] Clinical findings of drugs, medicaments and biological substances in blood, blood-forming organs, or the immune system\n --CHILD--> [MA12.2] Finding of hallucinogen in blood", "[MA12.1] Finding of cocaine in blood\n --PARENT--> [MA12] Clinical findings of drugs, medicaments and biological substances in blood, blood-forming organs, or the immune system\n --CHILD--> [MA12.0] Finding of opiate drug in blood" ]
3C0Z
Diseases of the blood or blood-forming organs, unspecified
[ { "from_icd11": "3C0Z", "icd10_code": "D75A", "icd10_title": "Glucose-6-phosphate dehydrogenase (G6PD) deficiency without anemia" }, { "from_icd11": "3C0Z", "icd10_code": "D7581", "icd10_title": "Myelofibrosis" }, { "from_icd11": "3C0Z", "icd10_code": "D7582", "icd10_title": "Heparin induced thrombocytopenia (HIT)" }, { "from_icd11": "3C0Z", "icd10_code": "D7589", "icd10_title": "Other specified diseases of blood and blood-forming organs" }, { "from_icd11": "3C0Z", "icd10_code": "D759", "icd10_title": "Disease of blood and blood-forming organs, unspecified" }, { "from_icd11": "3C0Z", "icd10_code": "D763", "icd10_title": "Other histiocytosis syndromes" }, { "from_icd11": "3C0Z", "icd10_code": "Q899", "icd10_title": "Congenital malformation, unspecified" }, { "from_icd11": "3C0Z", "icd10_code": "III", "icd10_title": "" }, { "from_icd11": "3C0Z", "icd10_code": "D70-D77", "icd10_title": "" }, { "from_icd11": "3C0Z", "icd10_code": "D75", "icd10_title": "Other and unspecified diseases of blood and blood-forming organs" }, { "from_icd11": "3C0Z", "icd10_code": "D77", "icd10_title": "Other disorders of blood and blood-forming organs in diseases classified elsewhere" }, { "from_icd11": "3C0Z", "icd10_code": "D758", "icd10_title": "Other specified diseases of blood and blood-forming organs" }, { "from_icd11": "3C0Z", "icd10_code": "D76", "icd10_title": "Other specified diseases with participation of lymphoreticular and reticulohistiocytic tissue" }, { "from_icd11": "MF50.4Z", "icd10_code": "R310", "icd10_title": "Gross hematuria" }, { "from_icd11": "MF50.4Z", "icd10_code": "R312", "icd10_title": "Other microscopic hematuria" } ]
D75A
Glucose-6-phosphate dehydrogenase (G6PD) deficiency without anemia