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vignette-icd-enriched

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Ms. R. is a 69-year-old woman with type 2 diabetes who has been treated with insulin since 2011. She is currently treated with basal-bolus insulin therapy that consists of once daily long-acting insulin analog and 3 rapid-acting insulin analog boluses with meals. Her diabetes control was poor for years, and in 4/2013 her A1c was 9.8%. Since 7/2014, her glycemic control has improved considerably with A1c levels ranging between 6.9% and 7.7%. She typically measures glucose 4 times/day before all meals and before bedtime. The frequency of her recorded hypoglycemia (glucose < 60 mg/dl) has been low at about 0.5 events per week without any nocturnal events. To achieve good glycemic control on insulin therapy, her insulin dosage has been adjusted 48 times over the past 28 weeks . Notably, her total daily insulin was increased by about 15% for a period of 5 months before it decreased to the original daily insulin dosage. Most of her dosage changes occurred in her long-acting insulin dose and her dinner rapid-acting insulin dose, although other components have changed as well. Fig. 1 d-Nav downloads for the index patients. The upper graph denotes total daily insulin over time. The lower graph denotes each component of the patient dosage, including long-acting insulin analog before bed and rapid-acting insulin analog with breakfast, lunch and dinner. Correction factors are not shown. a ) Ms. R.; b ) Mr. E
3.341797
0.962402
sec[0]/sec[0]/p[0]
en
0.999996
29682315
https://doi.org/10.1186/s40842-018-0056-5
[ "insulin", "acting", "daily", "analog", "long", "rapid", "control", "diabetes", "treated", "since" ]
[ { "code": "5A44", "title": "Insulin-resistance syndromes" }, { "code": "5A4Y", "title": "Other specified disorders of glucose regulation or pancreatic internal secretion" }, { "code": "QB51.5", "title": "Presence of endocrine implants" }, { "code": "EF02.0", "title": "Fat hypertrophy" }, { "code": "PK9C.2", "title": "Other or unspecified medical devices associated with injury or harm, prosthetic or other implants, materials or accessory devices" }, { "code": "MG55.0", "title": "Artemisinin resistant Plasmodium falciparum" }, { "code": "NE60", "title": "Harmful effects of drugs, medicaments or biological substances, not elsewhere classified" }, { "code": "PL14.1", "title": "Non provision of necessary procedure" }, { "code": "HA2Z", "title": "Sexual pain disorders, unspecified" }, { "code": "PB28", "title": "Unintentional exposure to or harmful effects of other or unspecified drug, medicament or biological substance" } ]
=== ICD-11 CODES FOUND === [5A44] Insulin-resistance syndromes Also known as: Insulin-resistance syndromes | Insulin-resistance syndrome type A | Insulin-resistance syndrome type B | Rabson-Mendenhall syndrome | Laminopathy type Decaudain-Vigouroux [5A4Y] Other specified disorders of glucose regulation or pancreatic internal secretion Also known as: Other specified disorders of glucose regulation or pancreatic internal secretion | Other hypoglycaemia | Hyperinsulinaemia | hyperinsulinism | functional hyperinsulinaemia [QB51.5] Presence of endocrine implants Also known as: Presence of endocrine implants | presence of insulin pump Includes: presence of insulin pump [EF02.0] Fat hypertrophy Definition: Focal hypertrophy of subcutaneous adipose tissue. It is a common sequela of long-term insulin injection into the skin. Also known as: Fat hypertrophy | Insulin-induced localised fat hypertrophy | Insulin-induced lipohypertrophy [PK9C.2] Other or unspecified medical devices associated with injury or harm, prosthetic or other implants, materials or accessory devices Also known as: Other or unspecified medical devices associated with injury or harm, prosthetic or other implants, materials or accessory devices | Surgical operation with implant of other or unspecified artificial internal device associated with abnormal reaction of the patient, or of later complication, without mention of misadventure at the time of the procedure | Mechanical complication of other specified internal prosthetic devices, implants and grafts | Mechanical complication of insulin pump Excludes: Circumstances associated with a surgical or other medical device influencing the episode of care without injury or harm [MG55.0] Artemisinin resistant Plasmodium falciparum Also known as: Artemisinin resistant Plasmodium falciparum | Antimicrobial resistant Plasmodium falciparum | multidrug-resistant falciparum malaria | artesunate monotherapy resistance | ACT - [artemisinin-based combination therapy] resistance [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 [PL14.1] 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 [HA2Z] Sexual pain disorders, unspecified Also known as: Sexual pain disorders, unspecified | Psychogenic dyspareunia | psychologic dyspareunia | psychologic painful sexual act of female | dyspareunia of nonorganic origin [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 === GRAPH WALKS === --- Walk 1 --- [5A44] Insulin-resistance syndromes --PARENT--> [?] Other disorders of glucose regulation or pancreatic internal secretion --RELATED_TO--> [?] PPoma Def: A benign or malignant neuroendocrine tumour that arises from the pancreas and secretes pancreatic polypeptide.... --- Walk 2 --- [5A44] Insulin-resistance syndromes --PARENT--> [?] Other disorders of glucose regulation or pancreatic internal secretion --RELATED_TO--> [?] Somatostatinoma Def: A rare, usually malignant neuroendocrine tumour arizing from delta cells. This neoplasm produces large amounts of somatostatin, which may result in a syndrome characterised by diarrhea, steatorrhea, w... --- Walk 3 --- [5A4Y] Other specified disorders of glucose regulation or pancreatic internal secretion --PARENT--> [?] Other disorders of glucose regulation or pancreatic internal secretion --RELATED_TO--> [?] Somatostatinoma Def: A rare, usually malignant neuroendocrine tumour arizing from delta cells. This neoplasm produces large amounts of somatostatin, which may result in a syndrome characterised by diarrhea, steatorrhea, w... --- Walk 4 --- [5A4Y] Other specified disorders of glucose regulation or pancreatic internal secretion --PARENT--> [?] Other disorders of glucose regulation or pancreatic internal secretion --EXCLUDES--> [?] Benign neoplasm of endocrine pancreas --- Walk 5 --- [QB51.5] Presence of endocrine implants --PARENT--> [QB51] Presence of devices other than cardiac or vascular implants --CHILD--> [QB51.2] Presence of intraocular lens --- Walk 6 --- [QB51.5] Presence of endocrine implants --PARENT--> [QB51] Presence of devices other than cardiac or vascular implants --CHILD--> [QB51.0] Presence of a neurostimulator
[ "[5A44] Insulin-resistance syndromes\n --PARENT--> [?] Other disorders of glucose regulation or pancreatic internal secretion\n --RELATED_TO--> [?] PPoma\n Def: A benign or malignant neuroendocrine tumour that arises from the pancreas and secretes pancreatic polypeptide....", "[5A44] Insulin-resistance syndromes\n --PARENT--> [?] Other disorders of glucose regulation or pancreatic internal secretion\n --RELATED_TO--> [?] Somatostatinoma\n Def: A rare, usually malignant neuroendocrine tumour arizing from delta cells. This neoplasm produces large amounts of somatostatin, which may result in a syndrome characterised by diarrhea, steatorrhea, w...", "[5A4Y] Other specified disorders of glucose regulation or pancreatic internal secretion\n --PARENT--> [?] Other disorders of glucose regulation or pancreatic internal secretion\n --RELATED_TO--> [?] Somatostatinoma\n Def: A rare, usually malignant neuroendocrine tumour arizing from delta cells. This neoplasm produces large amounts of somatostatin, which may result in a syndrome characterised by diarrhea, steatorrhea, w...", "[5A4Y] Other specified disorders of glucose regulation or pancreatic internal secretion\n --PARENT--> [?] Other disorders of glucose regulation or pancreatic internal secretion\n --EXCLUDES--> [?] Benign neoplasm of endocrine pancreas", "[QB51.5] Presence of endocrine implants\n --PARENT--> [QB51] Presence of devices other than cardiac or vascular implants\n --CHILD--> [QB51.2] Presence of intraocular lens", "[QB51.5] Presence of endocrine implants\n --PARENT--> [QB51] Presence of devices other than cardiac or vascular implants\n --CHILD--> [QB51.0] Presence of a neurostimulator" ]
5A44
Insulin-resistance syndromes
[ { "from_icd11": "5A44", "icd10_code": "E10-E14", "icd10_title": "" }, { "from_icd11": "QB51.5", "icd10_code": "Z9641", "icd10_title": "Presence of insulin pump (external) (internal)" }, { "from_icd11": "QB51.5", "icd10_code": "Z964", "icd10_title": "Presence of endocrine implants" }, { "from_icd11": "EF02.0", "icd10_code": "L988", "icd10_title": "Other specified disorders of the skin and subcutaneous tissue" }, { "from_icd11": "EF02.0", "icd10_code": "E881", "icd10_title": "Lipodystrophy, not elsewhere classified" }, { "from_icd11": "PK9C.2", "icd10_code": "T85694A", "icd10_title": "Other mechanical complication of insulin pump, initial encounter" }, { "from_icd11": "PK9C.2", "icd10_code": "T85614A", "icd10_title": "Breakdown (mechanical) of insulin pump, initial encounter" }, { "from_icd11": "PK9C.2", "icd10_code": "T85624A", "icd10_title": "Displacement of insulin pump, initial encounter" }, { "from_icd11": "PK9C.2", "icd10_code": "T85618A", "icd10_title": "Breakdown (mechanical) of other specified internal prosthetic devices, implants and grafts, initial encounter" }, { "from_icd11": "PK9C.2", "icd10_code": "T85628A", "icd10_title": "Displacement of other specified internal prosthetic devices, implants and grafts, initial encounter" }, { "from_icd11": "PK9C.2", "icd10_code": "T85621A", "icd10_title": "Displacement of intraperitoneal dialysis catheter, initial encounter" }, { "from_icd11": "PK9C.2", "icd10_code": "T85611A", "icd10_title": "Breakdown (mechanical) of intraperitoneal dialysis catheter, initial encounter" }, { "from_icd11": "PK9C.2", "icd10_code": "T85698A", "icd10_title": "Other mechanical complication of other specified internal prosthetic devices, implants and grafts, initial encounter" }, { "from_icd11": "PK9C.2", "icd10_code": "T85638A", "icd10_title": "Leakage of other specified internal prosthetic devices, implants and grafts, initial encounter" }, { "from_icd11": "PK9C.2", "icd10_code": "T85610A", "icd10_title": "Breakdown (mechanical) of cranial or spinal infusion catheter, initial encounter" } ]
E10-E14
A 13-year-old female presented with a history of a 40-day fever, abdominal pain for one month, and three days of limping before presentation. Initially, the fever was low-grade and responded to paracetamol; she was diagnosed with tonsilitis and was given amoxicillin at the health center without improvement. A week after the fever, she developed mild right-sided abdominal pain, relieved by applying pressure, such as lying down ipsilaterally, and aggravated by lying on the left side. Gradually, the pain worsened, as it progressed to the inguinal region and intensified while walking, which caused her to lean forward to minimize the pain. Additionally, she complained of vomiting after meals, especially in the morning, for two weeks before admission, which led to significant weight loss. She had no history of urinary tract infections, no history of preceding trauma, renal stones, or congenital anomalies; her family history was also unremarkable. Her temperature was 38.5 °C, pulse 139 bpm, respiration 25/min, blood pressure 87/54 mmHg, height 144 cm in the 10th percentile, and weight 30 kg in the 5th percentile. Physical examination revealed an alert and cooperative child with a fever. She had mild pallor, and there was right abdominal tenderness with no palpable masses. The hip was in a flexed position while another systemic exam was unremarkable. Laboratory investigations are illustrated in Table 1 .
3.71875
0.987305
sec[1]/p[0]
en
0.999998
PMC10518206
https://doi.org/10.7759/cureus.44118
[ "fever", "pain", "abdominal", "pressure", "lying", "while", "which", "weight", "unremarkable", "percentile" ]
[ { "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": "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" } ]
=== 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 [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 === 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.... --RELATED_TO--> [?] Pyrexia of unknown origin following delivery --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 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--> [1D81.0] 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 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.... --PARENT--> [01] Certain infectious or parasitic diseases Def: This chapter includes certain conditions caused by pathogenic organisms or microorganisms, such as bacteria, viruses, parasites or fungi.... --- 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--> [1B91] Leptospirosis Def: A disease caused by an infection with the gram-negative bacteria Leptospira. In the first phase, this disease is characterised by generalised illness (fever, chills, or myalgias) or individuals may be...
[ "[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--> [?] Pyrexia of unknown origin following delivery\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....", "[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--> [1D81.0] 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...", "[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 --PARENT--> [01] Certain infectious or parasitic diseases\n Def: This chapter includes certain conditions caused by pathogenic organisms or microorganisms, such as bacteria, viruses, parasites or fungi....", "[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--> [1B91] Leptospirosis\n Def: A disease caused by an infection with the gram-negative bacteria Leptospira. In the first phase, this disease is characterised by generalised illness (fever, chills, or myalgias) or individuals may be..." ]
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
A 30-year-old woman (G 2 P 1 , weight 62 kg, height 162 cm) with a 33-week gestation had dizziness, fatigue, dyspnea, and lower extremity edema for 1 week. She was diagnosed with congenital heart disease 10 years ago but remained asymptomatic without therapy until this time. She delivered a female baby by caesarean section without incident at another hospital 6 years ago. There was no other significant past medical history. Vital signs were HR 84 beats·min −1 , RR 20 breaths·min −1 , BP 125/80 mmHg, and S p O 2 58% on room air and 75%–88% on oxygen at 6 L·min −1 by facemask. She had marked cyanosis and clubbing of her fingers. Auscultation revealed a loud P 2 and a grade 5/6 systolic murmur in the pulmonary area. There was moderate lower extremity edema. Laboratory test results included Hb 14.5 g·dL −1 , Hct 45%, platelets 173 × 10 9 ·L −1 , ALT 271 g·L −1 , AST 184 g·L −1 , albumin 3.52 g·dL −1 , and normal PT and aPTT. Blood gases showed pH 7.35, P a O 2 61 mmHg, P a CO 2 34 mmHg, HCO 3 − 18.1 mmol·L −1 , base excess (BE) −6.6, and S a O 2 90.1%. Transthoracic echocardiography revealed a 20 mm VSD with bidirectional blood flow at rest, enlarged left ventricle (54 mm), mild dilation of the right atrium, hypertrophy of the right ventricle, mild tricuspid regurgitation, estimated systolic pulmonary artery pressure of 166 mmHg, mild pericardial effusion, and an estimated left ventricular EF of 61%.
4.042969
0.977539
sec[1]/sec[1]/p[0]
en
0.999998
21961000
https://doi.org/10.1155/2011/972671
[ "mmhg", "extremity", "edema", "without", "systolic", "pulmonary", "blood", "ventricle", "estimated", "weight" ]
[ { "code": "ND56.1", "title": "Open wound of unspecified body region" }, { "code": "LB9Z", "title": "Structural developmental anomalies of the skeleton, unspecified" }, { "code": "FB56.6", "title": "Other specified soft tissue disorders" }, { "code": "5B51&XS25", "title": "Severe wasting in infants, children or adolescents" }, { "code": "ND55", "title": "Other injuries of leg, level unspecified" }, { "code": "MG29.Z", "title": "Oedema, unspecified" }, { "code": "5B7Z", "title": "Unspecified undernutrition" }, { "code": "FA36.Z", "title": "Effusion of joint, unspecified" }, { "code": "JA22.1", "title": "Gestational oedema without hypertension" }, { "code": "MG29.1", "title": "Generalised oedema" } ]
=== ICD-11 CODES FOUND === [ND56.1] Open wound of unspecified body region Also known as: Open wound of unspecified body region | cut NOS | open wound NOS | penetrating wound NOS | Puncture wound with foreign body unspecified body region Excludes: Traumatic amputations involving multiple body regions | Open wounds involving multiple body regions | traumatic amputation NOS [LB9Z] Structural developmental anomalies of the skeleton, unspecified Also known as: Structural developmental anomalies of the skeleton, unspecified | Abnormal bone development | skeletal anomaly NOS [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 [ND55] Other injuries of leg, level unspecified Also known as: Other injuries of leg, level unspecified | other injuries of lower limb, level unspecified | Superficial injury of leg, level unspecified | Abrasion of leg, level unspecified | Contusion of leg, level unspecified Excludes: Fracture of leg, level unspecified | Injuries involving multiple body regions [MG29.Z] Oedema, unspecified Also known as: Oedema, unspecified | Oedema | dropsy | hydrops | Fluid retention NOS [5B7Z] Unspecified undernutrition Also known as: Unspecified undernutrition | Malnutrition NOS | nutritional deficiency NOS | nutritional depletion NOS | severe malnutrition NOS [FA36.Z] Effusion of joint, unspecified Also known as: Effusion of joint, unspecified | Effusion of joint | effusion into joint | effusion of joint, site unspecified | hydrarthrosis [JA22.1] Gestational oedema without hypertension Also known as: Gestational oedema without hypertension | oedema of pregnancy [MG29.1] Generalised oedema Also known as: Generalised oedema | anasarca === GRAPH WALKS === --- Walk 1 --- [ND56.1] Open wound of unspecified body region --EXCLUDES--> [?] Open wounds involving multiple body regions --EXCLUDES--> [?] Traumatic amputations involving multiple body regions --- Walk 2 --- [ND56.1] Open wound of unspecified body region --EXCLUDES--> [?] Traumatic amputations involving multiple body regions --EXCLUDES--> [?] Other injuries of leg, level unspecified --- Walk 3 --- [LB9Z] Structural developmental anomalies of the skeleton, unspecified --PARENT--> [?] Structural developmental anomalies of the skeleton Def: A deformation established before birth of an anatomical structure of one or more bones.... --CHILD--> [LB72] Structural developmental anomalies of shoulder girdle Def: Any condition caused by failure of the shoulder girdle to correctly develop during the antenatal period.... --- Walk 4 --- [LB9Z] Structural developmental anomalies of the skeleton, unspecified --PARENT--> [?] Structural developmental anomalies of the skeleton Def: A deformation established before birth of an anatomical structure of one or more bones.... --CHILD--> [LB71] Structural developmental anomalies of facial bones Def: Any condition caused by failure of the facial bones to correctly develop during the antenatal period.... --- Walk 5 --- [FB56.6] Other specified soft tissue disorders --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.... --CHILD--> [FB56.0] Foreign body granuloma of soft tissue, not elsewhere classified --- Walk 6 --- [FB56.6] Other specified soft tissue disorders --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.... --CHILD--> [FB56.1] Residual foreign body in soft tissue
[ "[ND56.1] Open wound of unspecified body region\n --EXCLUDES--> [?] Open wounds involving multiple body regions\n --EXCLUDES--> [?] Traumatic amputations involving multiple body regions", "[ND56.1] Open wound of unspecified body region\n --EXCLUDES--> [?] Traumatic amputations involving multiple body regions\n --EXCLUDES--> [?] Other injuries of leg, level unspecified", "[LB9Z] Structural developmental anomalies of the skeleton, unspecified\n --PARENT--> [?] Structural developmental anomalies of the skeleton\n Def: A deformation established before birth of an anatomical structure of one or more bones....\n --CHILD--> [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....", "[LB9Z] Structural developmental anomalies of the skeleton, unspecified\n --PARENT--> [?] Structural developmental anomalies of the skeleton\n Def: A deformation established before birth of an anatomical structure of one or more bones....\n --CHILD--> [LB71] Structural developmental anomalies of facial bones\n Def: Any condition caused by failure of the facial bones to correctly develop during the antenatal period....", "[FB56.6] Other specified soft tissue disorders\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 --CHILD--> [FB56.0] Foreign body granuloma of soft tissue, not elsewhere classified", "[FB56.6] Other specified soft tissue disorders\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 --CHILD--> [FB56.1] Residual foreign body in soft tissue" ]
ND56.1
Open wound of unspecified body region
[ { "from_icd11": "ND56.1", "icd10_code": "T141", "icd10_title": "" }, { "from_icd11": "LB9Z", "icd10_code": "Q8789", "icd10_title": "Other specified congenital malformation syndromes, not elsewhere classified" }, { "from_icd11": "LB9Z", "icd10_code": "Q8781", "icd10_title": "Alport syndrome" }, { "from_icd11": "LB9Z", "icd10_code": "Q742", "icd10_title": "Other congenital malformations of lower limb(s), including pelvic girdle" }, { "from_icd11": "LB9Z", "icd10_code": "Q749", "icd10_title": "Unspecified congenital malformation of limb(s)" }, { "from_icd11": "LB9Z", "icd10_code": "Q740", "icd10_title": "Other congenital malformations of upper limb(s), including shoulder girdle" }, { "from_icd11": "LB9Z", "icd10_code": "Q741", "icd10_title": "Congenital malformation of knee" }, { "from_icd11": "LB9Z", "icd10_code": "Q875", "icd10_title": "Other congenital malformation syndromes with other skeletal changes" }, { "from_icd11": "LB9Z", "icd10_code": "Q748", "icd10_title": "Other specified congenital malformations of limb(s)" }, { "from_icd11": "LB9Z", "icd10_code": "Q89", "icd10_title": "Other congenital malformations, not elsewhere classified" }, { "from_icd11": "LB9Z", "icd10_code": "Q65-Q79", "icd10_title": "" }, { "from_icd11": "LB9Z", "icd10_code": "Q73", "icd10_title": "Reduction defects of unspecified limb" }, { "from_icd11": "LB9Z", "icd10_code": "Q730", "icd10_title": "Congenital absence of unspecified limb(s)" }, { "from_icd11": "LB9Z", "icd10_code": "Q731", "icd10_title": "Phocomelia, unspecified limb(s)" }, { "from_icd11": "LB9Z", "icd10_code": "Q74", "icd10_title": "Other congenital malformations of limb(s)" } ]
T141
Endoscopic NJT placement is a simple and effective method. We have experienced over a 96% success rate using this technique . However, pushing the NJT blindly beyond the second portion of the duodenum may result in a kink in the distal end, especially in patients with stenosis of the duodenum or swelling in the tail of the pancreas. Endoscopic related pneumoretroperitoneum due to duodenal perforation has been reported . But in this patient, we initially thought that the duodenal perforation was not a complication of endoscopic NJT placement because it was not until the 16th day after placement that she had a high fever and abdominal distension. The patient tolerated EN well for 15 days. The duodenum is the lack of serous membrane. When it is surrounded by peripancreatic inflammation and fluid, it becomes swollen and fragile. In this patient, the NJT was kinking on the third portion of the duodenum. Additionally, the tip of the NJT had collided with the wall of the duodenum on the second portion for a long time. Duodenal perforation may occur when the pressure of the tip is not removed in time. Once the tip of the NJT was inserted into the retroperitoneum and EN was not stopped, retroperitoneal emphysema and an abscess occurred immediately. When NJT is placed using endoscopic techniques, the final position must be determined by an abdominal radiography and interpreted by the attending radiologist.
4.039063
0.538086
sec[2]/p[1]
en
0.999997
20509898
https://doi.org/10.1186/1752-1947-4-162
[ "duodenum", "endoscopic", "placement", "this", "portion", "duodenal", "perforation", "using", "that", "abdominal" ]
[ { "code": "DA5Z", "title": "Diseases of duodenum, unspecified" }, { "code": "DA51.Z", "title": "Duodenitis, unspecified" }, { "code": "DA50.0", "title": "Obstruction of duodenum" }, { "code": "DA63.Z", "title": "Duodenal ulcer, unspecified" }, { "code": "QF01.Y", "title": "Other specified acquired absence of organs" }, { "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 === [DA5Z] Diseases of duodenum, unspecified Also known as: Diseases of duodenum, unspecified | disorder of duodenum | duodenum disease NOS | duodenal disease NOS | duodenopathy NOS [DA51.Z] Duodenitis, unspecified Also known as: Duodenitis, unspecified | Duodenitis | nonspecific duodenitis | Inflammation of duodenum | dodecadactylitis [DA50.0] Obstruction of duodenum Definition: Hindrance of the passage of luminal contents in the duodenum. Obstruction of duodenum can be partial or complete, and caused by intrinsic or extrinsic factors. Simple obstruction is associated with diminished or stopped flow of luminal contents. Strangulating obstruction is associated with impaired blood flow to the duodenum in addition to obstructed flow of luminal contents. Also known as: Obstruction of duodenum | duodenal obstruction | obstructed duodenum | Aortomesenteric duodenum occlusion syndrome | Duodenal ileus Excludes: congenital stenosis of duodenum [DA63.Z] Duodenal ulcer, unspecified Also known as: Duodenal ulcer, unspecified | Duodenal ulcer | duodenal peptic ulcer [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 [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 --- [DA5Z] Diseases of duodenum, unspecified --PARENT--> [?] Diseases of duodenum Def: This is a group of conditions characterised as being in or associated with the duodenum, the first portion of the small intestine.... --CHILD--> [DA51] Duodenitis Def: Duodenitis is an injury of duodenal mucosa that involves epithelial damage and mucosal inflammation except for any epithelial defect. Duodenitis is caused by various factors such as high acid secretio... --- Walk 2 --- [DA5Z] Diseases of duodenum, unspecified --PARENT--> [?] Diseases of duodenum Def: This is a group of conditions characterised as being in or associated with the duodenum, the first portion of the small intestine.... --RELATED_TO--> [?] Duodenal ulcer Def: Duodenal ulcer is defined as a distinct breach in the mucosa of the duodenum as a result of caustic effects of acid and pepsin in the lumen. Histologically, duodenal ulcer is identified as necrosis of... --- Walk 3 --- [DA51.Z] Duodenitis, unspecified --PARENT--> [DA51] Duodenitis Def: Duodenitis is an injury of duodenal mucosa that involves epithelial damage and mucosal inflammation except for any epithelial defect. Duodenitis is caused by various factors such as high acid secretio... --CHILD--> [DA51.2] Lymphocytic duodenitis Def: Chronic duodenitis characterised by a dense infiltration of benign lymphocytes into the epithelium and lamina propria. Lymphocytic duodenitis may present early gluten-induced damage.... --- Walk 4 --- [DA51.Z] Duodenitis, unspecified --PARENT--> [DA51] Duodenitis Def: Duodenitis is an injury of duodenal mucosa that involves epithelial damage and mucosal inflammation except for any epithelial defect. Duodenitis is caused by various factors such as high acid secretio... --PARENT--> [?] Diseases of duodenum Def: This is a group of conditions characterised as being in or associated with the duodenum, the first portion of the small intestine.... --- Walk 5 --- [DA50.0] Obstruction of duodenum Def: Hindrance of the passage of luminal contents in the duodenum. Obstruction of duodenum can be partial or complete, and caused by intrinsic or extrinsic factors. Simple obstruction is associated with di... --EXCLUDES--> [?] Atresia of duodenum Def: Duodenal atresia is an embryopathy of the cranial intestine that leads to a complete absence of the duodenal lumen. In 30-52% of infants it is an isolated anomaly, but it is often associated with othe... --PARENT--> [?] Structural developmental anomalies of duodenum Def: Any congenital defect of duodenum 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 in ... --- Walk 6 --- [DA50.0] Obstruction of duodenum Def: Hindrance of the passage of luminal contents in the duodenum. Obstruction of duodenum can be partial or complete, and caused by intrinsic or extrinsic factors. Simple obstruction is associated with di... --EXCLUDES--> [?] Atresia of duodenum Def: Duodenal atresia is an embryopathy of the cranial intestine that leads to a complete absence of the duodenal lumen. In 30-52% of infants it is an isolated anomaly, but it is often associated with othe... --PARENT--> [?] Structural developmental anomalies of duodenum Def: Any congenital defect of duodenum 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 in ...
[ "[DA5Z] Diseases of duodenum, unspecified\n --PARENT--> [?] Diseases of duodenum\n Def: This is a group of conditions characterised as being in or associated with the duodenum, the first portion of the small intestine....\n --CHILD--> [DA51] Duodenitis\n Def: Duodenitis is an injury of duodenal mucosa that involves epithelial damage and mucosal inflammation except for any epithelial defect. Duodenitis is caused by various factors such as high acid secretio...", "[DA5Z] Diseases of duodenum, unspecified\n --PARENT--> [?] Diseases of duodenum\n Def: This is a group of conditions characterised as being in or associated with the duodenum, the first portion of the small intestine....\n --RELATED_TO--> [?] Duodenal ulcer\n Def: Duodenal ulcer is defined as a distinct breach in the mucosa of the duodenum as a result of caustic effects of acid and pepsin in the lumen. Histologically, duodenal ulcer is identified as necrosis of...", "[DA51.Z] Duodenitis, unspecified\n --PARENT--> [DA51] Duodenitis\n Def: Duodenitis is an injury of duodenal mucosa that involves epithelial damage and mucosal inflammation except for any epithelial defect. Duodenitis is caused by various factors such as high acid secretio...\n --CHILD--> [DA51.2] Lymphocytic duodenitis\n Def: Chronic duodenitis characterised by a dense infiltration of benign lymphocytes into the epithelium and lamina propria. Lymphocytic duodenitis may present early gluten-induced damage....", "[DA51.Z] Duodenitis, unspecified\n --PARENT--> [DA51] Duodenitis\n Def: Duodenitis is an injury of duodenal mucosa that involves epithelial damage and mucosal inflammation except for any epithelial defect. Duodenitis is caused by various factors such as high acid secretio...\n --PARENT--> [?] Diseases of duodenum\n Def: This is a group of conditions characterised as being in or associated with the duodenum, the first portion of the small intestine....", "[DA50.0] Obstruction of duodenum\n Def: Hindrance of the passage of luminal contents in the duodenum. Obstruction of duodenum can be partial or complete, and caused by intrinsic or extrinsic factors. Simple obstruction is associated with di...\n --EXCLUDES--> [?] Atresia of duodenum\n Def: Duodenal atresia is an embryopathy of the cranial intestine that leads to a complete absence of the duodenal lumen. In 30-52% of infants it is an isolated anomaly, but it is often associated with othe...\n --PARENT--> [?] Structural developmental anomalies of duodenum\n Def: Any congenital defect of duodenum 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 in ...", "[DA50.0] Obstruction of duodenum\n Def: Hindrance of the passage of luminal contents in the duodenum. Obstruction of duodenum can be partial or complete, and caused by intrinsic or extrinsic factors. Simple obstruction is associated with di...\n --EXCLUDES--> [?] Atresia of duodenum\n Def: Duodenal atresia is an embryopathy of the cranial intestine that leads to a complete absence of the duodenal lumen. In 30-52% of infants it is an isolated anomaly, but it is often associated with othe...\n --PARENT--> [?] Structural developmental anomalies of duodenum\n Def: Any congenital defect of duodenum 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 in ..." ]
DA5Z
Diseases of duodenum, unspecified
[ { "from_icd11": "DA51.Z", "icd10_code": "K2980", "icd10_title": "Duodenitis without bleeding" }, { "from_icd11": "DA51.Z", "icd10_code": "K2981", "icd10_title": "Duodenitis with bleeding" }, { "from_icd11": "DA51.Z", "icd10_code": "K2990", "icd10_title": "Gastroduodenitis, unspecified, without bleeding" }, { "from_icd11": "DA51.Z", "icd10_code": "K2991", "icd10_title": "Gastroduodenitis, unspecified, with bleeding" }, { "from_icd11": "DA51.Z", "icd10_code": "K29", "icd10_title": "Gastritis and duodenitis" }, { "from_icd11": "DA51.Z", "icd10_code": "K298", "icd10_title": "Duodenitis" }, { "from_icd11": "DA51.Z", "icd10_code": "K299", "icd10_title": "Gastroduodenitis, unspecified" }, { "from_icd11": "DA50.0", "icd10_code": "K315", "icd10_title": "Obstruction of duodenum" }, { "from_icd11": "DA63.Z", "icd10_code": "K265", "icd10_title": "Chronic or unspecified duodenal ulcer with perforation" }, { "from_icd11": "DA63.Z", "icd10_code": "K269", "icd10_title": "Duodenal ulcer, unspecified as acute or chronic, without hemorrhage or perforation" }, { "from_icd11": "DA63.Z", "icd10_code": "K264", "icd10_title": "Chronic or unspecified duodenal ulcer with hemorrhage" }, { "from_icd11": "DA63.Z", "icd10_code": "K260", "icd10_title": "Acute duodenal ulcer with hemorrhage" }, { "from_icd11": "DA63.Z", "icd10_code": "K261", "icd10_title": "Acute duodenal ulcer with perforation" }, { "from_icd11": "DA63.Z", "icd10_code": "K267", "icd10_title": "Chronic duodenal ulcer without hemorrhage or perforation" }, { "from_icd11": "DA63.Z", "icd10_code": "K266", "icd10_title": "Chronic or unspecified duodenal ulcer with both hemorrhage and perforation" } ]
K2980
Duodenitis without bleeding
The surgery required the deployment of four trocars. A 12-mm trocar was inserted through the umbilicus to establish pneumoperitoneum. Another 12-mm trocar was inserted below the xiphoid process, and 5-mm trocars were inserted in the right subcostal and flank regions. The boundary between the liver parenchyma and the cyst was determined via laparoscopic ultrasound sonography. A double-balloon catheter (S.A.N.D. balloon catheter, Hakko, Japan) was used to puncture the cystic wall and perform cystic fluid aspiration . Cytological examination confirmed the absence of malignancy before deroofing. The cystic fluid was serous, with bilirubin levels within normal limits (total bilirubin of 0.1 mg/dl). Using a vessel sealing device (Ligasure Medtronic, USA), the cystic wall was deroofed, revealing a bile leak originating from the cyst’s inner region . Laparoscopically, the orifice of the bile leakage was identified and closed using a 4-0 monofilament absorbable suture . The cessation of the bile leakage was confirmed and a drainage tube was inserted. The total operative time was 193 minutes and the volume of fluid drained from the cyst was 3190 ml. No bile leakage was observed postoperatively, and she was discharged on the 7th postoperative day. Pathological examination of the excised cystic wall revealed a simple hepatic cyst. No cyst recurrence was observed via CT and ultrasound 18 months after surgery.
3.857422
0.961426
sec[1]/p[1]
en
0.999998
38544677
https://doi.org/10.1093/jscr/rjae176
[ "cyst", "cystic", "bile", "wall", "fluid", "leakage", "trocars", "trocar", "ultrasound", "balloon" ]
[ { "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": "CA25.Z", "title": "Cystic fibrosis, unspecified" }, { "code": "CB40.Y", "title": "Other specified diseases of the respiratory system" }, { "code": "GB71.0", "title": "Calculus in bladder" }, { "code": "DB99.1Z", "title": "Hepatic cyst, unspecified" }, { "code": "5A01.2", "title": "Nontoxic multinodular goitre" } ]
=== 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 [CA25.Z] Cystic fibrosis, unspecified Also known as: Cystic fibrosis, unspecified | Cystic fibrosis | mucoviscidosis | CF - [cystic fibrosis] | cystic fibrosis nos [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 [GB71.0] Calculus in bladder Definition: A condition caused by dehydration, decreased urine volume or fluid flow rates, or increased excretion of minerals such as calcium, oxalate, magnesium, cystine, and phosphate. This condition is characterised by urinary calculi located in the bladder. This condition may also present with haematuria, dysuria, or pain in the flank, lower abdomen, or groin. Confirmation is by abdominal radiography, to determine the presence and location of calculi. Also known as: Calculus in bladder | Urinary bladder stone | bladder calculi | bladder stone | urinary bladder calculus Includes: Urinary bladder stone Excludes: Calculus in a bowel segment for urinary diversion (e.g. neobladder, pouch) (NFBC) [DB99.1Z] Hepatic cyst, unspecified Also known as: Hepatic cyst, unspecified | Hepatic cyst | cyst of liver | cystic liver | liver cyst [5A01.2] Nontoxic multinodular goitre Definition: Multiple nodules of the thyroid gland due to follicular multiplication, unaccompanied by hyperthyroidism or thyrotoxicosis Also known as: Nontoxic multinodular goitre | non-toxic multinodular goitre | multinodular nontoxic struma | cystic goitre | Cystic goitre NOS === 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... --PARENT--> [FB80] Certain specified disorders of bone density or structure --CHILD--> [FB80.1] Skeletal fluorosis --- 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... --PARENT--> [FB80] Certain specified disorders of bone density or structure --RELATED_TO--> [?] Osteogenesis imperfecta Def: Osteogenesis imperfecta (OI) comprises a heterogeneous group of genetic disorders characterised by increased bone fragility, low bone mass, and susceptibility to bone fractures with variable severity.... --- Walk 3 --- [EK70.Z] Cutaneous cysts, unspecified --PARENT--> [EK70] Cutaneous cysts --RELATED_TO--> [?] Neonatal milia --- Walk 4 --- [EK70.Z] Cutaneous cysts, unspecified --PARENT--> [EK70] Cutaneous cysts --PARENT--> [?] Benign proliferations, neoplasms and cysts of the skin --- 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--> [FB42] Certain specified disorders of synovium or tendon --- 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 --PARENT--> [FB80] Certain specified disorders of bone density or structure\n --CHILD--> [FB80.1] Skeletal fluorosis", "[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 --PARENT--> [FB80] Certain specified disorders of bone density or structure\n --RELATED_TO--> [?] Osteogenesis imperfecta\n Def: Osteogenesis imperfecta (OI) comprises a heterogeneous group of genetic disorders characterised by increased bone fragility, low bone mass, and susceptibility to bone fractures with variable severity....", "[EK70.Z] Cutaneous cysts, unspecified\n --PARENT--> [EK70] Cutaneous cysts\n --RELATED_TO--> [?] Neonatal milia", "[EK70.Z] Cutaneous cysts, unspecified\n --PARENT--> [EK70] Cutaneous cysts\n --PARENT--> [?] Benign proliferations, neoplasms and cysts of the skin", "[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", "[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": "CA25.Z", "icd10_code": "E8419", "icd10_title": "Cystic fibrosis with other intestinal manifestations" }, { "from_icd11": "CA25.Z", "icd10_code": "E848", "icd10_title": "Cystic fibrosis with other manifestations" }, { "from_icd11": "CA25.Z", "icd10_code": "E849", "icd10_title": "Cystic fibrosis, unspecified" }, { "from_icd11": "CA25.Z", "icd10_code": "E84", "icd10_title": "Cystic fibrosis" }, { "from_icd11": "CA25.Z", "icd10_code": "E841", "icd10_title": "Cystic fibrosis with intestinal manifestations" } ]
M85412
Solitary bone cyst, left shoulder
In 2012, a 19-year-old male presented to the emergency room of our university hospital with a primary complaint of acute chest pain. The day before, the patient was seen by his general practitioner because of high fever (up to 40 °C), sore throat, cough, and cervical lymphadenopathy. The general practitioner performed a throat swab, which was positive for S. pyogenes . Consequently, Penicillin V was administered, and the patient was discharged. However, because of severe chest pain, the patient presented to our emergency room the following day. The ECG showed ST-segment elevations in leads II, III, aVF, and V4–V6 , the cardiac enzymes were significantly elevated (CK 858 U/L with a CK-MB fraction of 9.7%, hs-Troponin T 1042 ng/L (reference range: <14 ng/L)). The patient was admitted to the intensive care unit (ICU) for continuous monitoring. No abnormalities could be seen upon echocardiography; systolic left ventricular function was normal with no apparent regional wall motion abnormalities. Cardiac MRI showed subepicardial late enhancement in the area of the apex as well as the apical and midventricular anterolateral wall and the adjacent posterior wall . Moreover, there was mild pericardial late enhancement suggestive of pericardial involvement. Furthermore, moderate apical and midventricular hypokinesia, as well as discrete dilatation of the LV (LVIDd 59 mm, LVEF 51%), became apparent upon MRI.
4.003906
0.979004
sec[1]/p[0]
en
0.999998
35735799
https://doi.org/10.3390/jcdd9060170
[ "wall", "emergency", "room", "chest", "pain", "general", "practitioner", "because", "throat", "cardiac" ]
[ { "code": "LB0Y", "title": "Other specified structural developmental anomalies of the diaphragm, abdominal wall or umbilical cord" }, { "code": "PA82", "title": "Unintentional striking against stationary object" }, { "code": "NB50.Y&XA3KX0&XJ1C6", "title": "Haematoma of abdominal wall" }, { "code": "DC51.1", "title": "Peritoneal adhesions" }, { "code": "LB73.1Z", "title": "Structural developmental anomalies of chest wall, unspecified" }, { "code": "JB22.1", "title": "Delivery by emergency caesarean section" }, { "code": "RA09", "title": "International emergency code 10" }, { "code": "BA03", "title": "Hypertensive crisis" }, { "code": "RA00", "title": "Conditions of uncertain aetiology and emergency use" }, { "code": "RA04", "title": "International emergency code 05" } ]
=== ICD-11 CODES FOUND === [LB0Y] Other specified structural developmental anomalies of the diaphragm, abdominal wall or umbilical cord Also known as: Other specified structural developmental anomalies of the diaphragm, abdominal wall or umbilical cord | Congenital deformity of abdominal wall | abdominal wall defect NOS [PA82] Unintentional striking against stationary object Also known as: Unintentional striking against stationary object | striking against stationary object | striking against or struck by other objects | Walked into wall [DC51.1] Peritoneal adhesions Definition: Disorders of peritoneum sticking by scar tissue or fibrosis Also known as: Peritoneal adhesions | abdominal adhesion | adhesive peritoneal band | peritoneal adhesion | peritoneal band Excludes: Adhesions of large intestine with obstruction | Postprocedural pelvic peritoneal adhesions | Intestinal adhesions or bands of small intestine with obstruction [LB73.1Z] Structural developmental anomalies of chest wall, unspecified Also known as: Structural developmental anomalies of chest wall, unspecified | Structural developmental anomalies of chest wall | Malformations of chest wall [JB22.1] Delivery by emergency caesarean section Also known as: Delivery by emergency caesarean section | emergency caesarean [RA09] International emergency code 10 Also known as: International emergency code 10 [BA03] Hypertensive crisis Also known as: Hypertensive crisis | Hypertensive emergency | hypertensive crisis with acute organ damage | severely elevated blood pressure with acute organ damage | Hypertensive urgency [RA00] Conditions of uncertain aetiology and emergency use Also known as: Conditions of uncertain aetiology and emergency use [RA04] International emergency code 05 Also known as: International emergency code 05 === GRAPH WALKS === --- Walk 1 --- [LB0Y] Other specified structural developmental anomalies of the diaphragm, abdominal wall or umbilical cord --PARENT--> [?] Structural developmental anomalies of the diaphragm, abdominal wall or umbilical cord Def: Any condition caused by failure of the diaphragm, abdominal wall or umbilical cord to correctly develop during the antenatal period.... --CHILD--> [LB01] Omphalocele Def: Omphalocele is an embryopathy classified in the group of abdominal celosomias and is characterised by a large hernia of the abdominal wall, centred on the umbilical cord, in which the protruding visce... --- Walk 2 --- [LB0Y] Other specified structural developmental anomalies of the diaphragm, abdominal wall or umbilical cord --PARENT--> [?] Structural developmental anomalies of the diaphragm, abdominal wall or umbilical cord Def: Any condition caused by failure of the diaphragm, abdominal wall or umbilical cord to correctly develop during the antenatal period.... --EXCLUDES--> [?] Prune belly syndrome Def: A syndrome is characterised by cryptorchidism, urinary tract defects, and poor development of the abdominal muscles causing the skin on the abdomen to wrinkle.... --- Walk 3 --- [PA82] Unintentional striking against stationary object --PARENT--> [?] Unintentional exposure to object, not elsewhere classified --CHILD--> [PA81] Unintentionally struck by moving object --- Walk 4 --- [PA82] Unintentional striking against stationary object --PARENT--> [?] Unintentional exposure to object, not elsewhere classified --CHILD--> [PA80] Unintentionally struck by projectile from firearm --- Walk 5 --- [DC51.1] Peritoneal adhesions Def: Disorders of peritoneum sticking by scar tissue or fibrosis... --EXCLUDES--> [?] Postprocedural pelvic peritoneal adhesions Def: A condition caused by or subsequent to any pelvic intervention leading to damage and inflammation of the peritoneum. This condition is characterised by fibrous bands of scar tissue and abnormal connec... --EXCLUDES--> [?] Endometriosis Def: A condition of the uterus that is frequently idiopathic. This condition is characterised by ectopic growth and function of endometrial tissue outside the uterine cavity. This condition may be associat... --- Walk 6 --- [DC51.1] Peritoneal adhesions Def: Disorders of peritoneum sticking by scar tissue or fibrosis... --EXCLUDES--> [?] Intestinal adhesions or bands of small intestine with obstruction Def: Small bowel obstruction resulting from intraabdominal adhesion due to laparotomy, trauma, and intraabdominal inflammation such as endometriosis.... --CHILD--> [?] Postoperative obstruction of the small intestine
[ "[LB0Y] Other specified structural developmental anomalies of the diaphragm, abdominal wall or umbilical cord\n --PARENT--> [?] Structural developmental anomalies of the diaphragm, abdominal wall or umbilical cord\n Def: Any condition caused by failure of the diaphragm, abdominal wall or umbilical cord to correctly develop during the antenatal period....\n --CHILD--> [LB01] Omphalocele\n Def: Omphalocele is an embryopathy classified in the group of abdominal celosomias and is characterised by a large hernia of the abdominal wall, centred on the umbilical cord, in which the protruding visce...", "[LB0Y] Other specified structural developmental anomalies of the diaphragm, abdominal wall or umbilical cord\n --PARENT--> [?] Structural developmental anomalies of the diaphragm, abdominal wall or umbilical cord\n Def: Any condition caused by failure of the diaphragm, abdominal wall or umbilical cord to correctly develop during the antenatal period....\n --EXCLUDES--> [?] Prune belly syndrome\n Def: A syndrome is characterised by cryptorchidism, urinary tract defects, and poor development of the abdominal muscles causing the skin on the abdomen to wrinkle....", "[PA82] Unintentional striking against stationary object\n --PARENT--> [?] Unintentional exposure to object, not elsewhere classified\n --CHILD--> [PA81] Unintentionally struck by moving object", "[PA82] Unintentional striking against stationary object\n --PARENT--> [?] Unintentional exposure to object, not elsewhere classified\n --CHILD--> [PA80] Unintentionally struck by projectile from firearm", "[DC51.1] Peritoneal adhesions\n Def: Disorders of peritoneum sticking by scar tissue or fibrosis...\n --EXCLUDES--> [?] Postprocedural pelvic peritoneal adhesions\n Def: A condition caused by or subsequent to any pelvic intervention leading to damage and inflammation of the peritoneum. This condition is characterised by fibrous bands of scar tissue and abnormal connec...\n --EXCLUDES--> [?] Endometriosis\n Def: A condition of the uterus that is frequently idiopathic. This condition is characterised by ectopic growth and function of endometrial tissue outside the uterine cavity. This condition may be associat...", "[DC51.1] Peritoneal adhesions\n Def: Disorders of peritoneum sticking by scar tissue or fibrosis...\n --EXCLUDES--> [?] Intestinal adhesions or bands of small intestine with obstruction\n Def: Small bowel obstruction resulting from intraabdominal adhesion due to laparotomy, trauma, and intraabdominal inflammation such as endometriosis....\n --CHILD--> [?] Postoperative obstruction of the small intestine" ]
LB0Y
Other specified structural developmental anomalies of the diaphragm, abdominal wall or umbilical cord
[ { "from_icd11": "PA82", "icd10_code": "W2209XA", "icd10_title": "Striking against other stationary object, initial encounter" }, { "from_icd11": "PA82", "icd10_code": "W2201XA", "icd10_title": "Walked into wall, initial encounter" }, { "from_icd11": "PA82", "icd10_code": "W2211XA", "icd10_title": "Striking against or struck by driver side automobile airbag, initial encounter" }, { "from_icd11": "PA82", "icd10_code": "W228XXS", "icd10_title": "Striking against or struck by other objects, sequela" }, { "from_icd11": "PA82", "icd10_code": "W2203XD", "icd10_title": "Walked into furniture, subsequent encounter" }, { "from_icd11": "PA82", "icd10_code": "W2203XA", "icd10_title": "Walked into furniture, initial encounter" }, { "from_icd11": "PA82", "icd10_code": "W228XXD", "icd10_title": "Striking against or struck by other objects, subsequent encounter" }, { "from_icd11": "PA82", "icd10_code": "W2212XA", "icd10_title": "Striking against or struck by front passenger side automobile airbag, initial encounter" }, { "from_icd11": "PA82", "icd10_code": "W2209XS", "icd10_title": "Striking against other stationary object, sequela" }, { "from_icd11": "PA82", "icd10_code": "W228XXA", "icd10_title": "Striking against or struck by other objects, initial encounter" }, { "from_icd11": "PA82", "icd10_code": "W22", "icd10_title": "Striking against or struck by other objects" }, { "from_icd11": "DC51.1", "icd10_code": "K660", "icd10_title": "Peritoneal adhesions (postprocedural) (postinfection)" }, { "from_icd11": "LB73.1Z", "icd10_code": "Q766", "icd10_title": "Other congenital malformations of ribs" }, { "from_icd11": "JB22.1", "icd10_code": "O821", "icd10_title": "" } ]
W2209XA
Striking against other stationary object, initial encounter
Echocardiography revealed preserved left ventricular ejection fraction (56%) with akinetic basal and mid segments of the inferior and posterior walls. Coronary angiography revealed significant luminal narrowing of proximal and mid segments of the RCA with a proximal linear filling defect and TIMI III flow to the distal RCA, in addition to persistence of the LAD and LCX aneurysms. Compared to the previous angiogram four years ago, the mid segment of the LAD showed an area of moderate (50%) narrowing with evident angiographic haziness . Intra-vascular ultrasound (IVUS) of the 3 vessels using 20 MHz Eagle Eye Platinum catheter (Volcano Corp.) revealed intimal thickening of the walls of the LAD and LCX aneurysms with no evidence of atherosclerosis and maximal lumen diameter of 7.8 and 7.5 mm respectively . The mid segment of the LAD aneurysm showed a mildly organized thrombus occupying the vessel lumen and causing 40% minimum lumen area (MLA) stenosis with MLA of 6 mm 2 . IVUS of the RCA showed a large aneurysm affecting the proximal and mid segments of the RCA with maximal lumen diameter 8.2 mm and minimally thickened concentric intima at the mid-section of the aneurysm with the proximal and distal parts of the aneurysm partially occluded by large, organized thrombi and segments showing poorly organized thrombi with areas of recanalization and calcification (linear defects by coronary angiography) .
4.230469
0.689453
sec[1]/p[1]
en
0.999997
29564353
https://doi.org/10.21542/gcsp.2017.32
[ "segments", "lumen", "aneurysm", "organized", "walls", "coronary", "angiography", "narrowing", "linear", "aneurysms" ]
[ { "code": "ME93.0", "title": "Segmental and somatic dysfunction" }, { "code": "8A06.1", "title": "Segmental myoclonus" }, { "code": "EC23.0", "title": "Non-syndromic genetically-determined hypermelanosis or lentiginosis" }, { "code": "GB40/MF8Y&XT8W", "title": "Chronic nephritic syndrome : focal and segmental glomerular lesions" }, { "code": "LB73.24", "title": "Segmentation anomalies of vertebrae" }, { "code": "BD51.Z", "title": "Aneurysm and dissection of unspecified artery" }, { "code": "BD75.Y", "title": "Venous varicosities of other specified sites" }, { "code": "BA81", "title": "Coronary artery aneurysm" }, { "code": "BB02.1Z", "title": "Aneurysm of pulmonary artery, unspecified" }, { "code": "BD51.4", "title": "Aneurysm or dissection of renal artery" } ]
=== ICD-11 CODES FOUND === [ME93.0] Segmental and somatic dysfunction Also known as: Segmental and somatic dysfunction | segmental dysfunction | somatic dysfunction | Segmental and somatic dysfunction, head region | Segmental and somatic dysfunction, occipitocervical region [8A06.1] Segmental myoclonus Definition: Rhythmic or semi-rhythmic involuntary contractions of muscle groups supplied by one or more contiguous segments of the brainstem and/or spinal cord. Also known as: Segmental myoclonus | Spinal segmental myoclonus | Propriospinal myoclonus [EC23.0] Non-syndromic genetically-determined hypermelanosis or lentiginosis Also known as: Non-syndromic genetically-determined hypermelanosis or lentiginosis | Familial progressive hyperpigmentation | Familial generalised lentiginosis | Inherited patterned lentiginosis | Centrofacial lentiginosis [LB73.24] Segmentation anomalies of vertebrae Definition: Any condition caused by failure of the vertebrae to correctly develop during the antenatal period. These conditions are characterised by an abnormal number of fully developed vertebrae. Confirmation is through verification of absent or improperly formed vertebrae by imaging. Also known as: Segmentation anomalies of vertebrae | Isolated hemivertebra | Multiple segmentation anomalies of vertebrae [BD51.Z] Aneurysm and dissection of unspecified artery Also known as: Aneurysm and dissection of unspecified artery | Arterial aneurysm or dissection, excluding aorta | cirsoid aneurysm NOS | false aneurysm NOS | ruptured aneurysm NOS [BD75.Y] Venous varicosities of other specified sites Also known as: Venous varicosities of other specified sites | Caput medusae | Jugular venous aneurysm | jugular vein aneurysm | Orbital varices [BA81] Coronary artery aneurysm Definition: Coronary dilatation which exceeds the diameter of normal adjacent segments or the diameter of the patient's largest coronary vessel by 1.5 times. Also known as: Coronary artery aneurysm | aneurysm of coronary vessels | aneurysmal lesion of coronary artery | arteriovenous aneurysm of coronary vessels | coronary aneurysm Excludes: Congenital coronary arterial aneurysm | Mucocutaneous lymph node syndrome [BB02.1Z] Aneurysm of pulmonary artery, unspecified Also known as: Aneurysm of pulmonary artery, unspecified | Aneurysm of pulmonary artery | pulmonary artery aneurysm | PA - [pulmonary artery aneurysm] | pulmonary aneurysm [BD51.4] Aneurysm or dissection of renal artery Also known as: Aneurysm or dissection of renal artery | aneurysm of renal artery | renal artery aneurysm | renal aneurysm === GRAPH WALKS === --- Walk 1 --- [ME93.0] Segmental and somatic dysfunction --PARENT--> [ME93] Biomechanical lesions, not elsewhere classified --CHILD--> [ME93.1] Subluxation stenosis of neural canal --- Walk 2 --- [ME93.0] Segmental and somatic dysfunction --PARENT--> [ME93] Biomechanical lesions, not elsewhere classified --CHILD--> [ME93.2] Osseous stenosis of neural canal --- Walk 3 --- [8A06.1] Segmental myoclonus Def: Rhythmic or semi-rhythmic involuntary contractions of muscle groups supplied by one or more contiguous segments of the brainstem and/or spinal cord.... --PARENT--> [8A06] Myoclonic disorders --EXCLUDES--> [?] 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 4 --- [8A06.1] Segmental myoclonus Def: Rhythmic or semi-rhythmic involuntary contractions of muscle groups supplied by one or more contiguous segments of the brainstem and/or spinal cord.... --PARENT--> [8A06] Myoclonic disorders --PARENT--> [?] Movement disorders Def: This is a group of involuntary movement disorders.... --- Walk 5 --- [EC23.0] Non-syndromic genetically-determined hypermelanosis or lentiginosis --PARENT--> [EC23] Genetic disorders of skin pigmentation Def: Genetic disorders of the skin characterised by disordered pigmentation, including albinism and inherited forms of lentiginosis.... --PARENT--> [?] Genetic or developmental disorders affecting the skin Def: A large group of disorders, some limited to the skin but many involving other organ systems, due to heritable genetic defects, chromosomal abnormalities or embryofetal developmental anomalies.... --- Walk 6 --- [EC23.0] Non-syndromic genetically-determined hypermelanosis or lentiginosis --PARENT--> [EC23] Genetic disorders of skin pigmentation Def: Genetic disorders of the skin characterised by disordered pigmentation, including albinism and inherited forms of lentiginosis.... --CHILD--> [EC23.0] Non-syndromic genetically-determined hypermelanosis or lentiginosis
[ "[ME93.0] Segmental and somatic dysfunction\n --PARENT--> [ME93] Biomechanical lesions, not elsewhere classified\n --CHILD--> [ME93.1] Subluxation stenosis of neural canal", "[ME93.0] Segmental and somatic dysfunction\n --PARENT--> [ME93] Biomechanical lesions, not elsewhere classified\n --CHILD--> [ME93.2] Osseous stenosis of neural canal", "[8A06.1] Segmental myoclonus\n Def: Rhythmic or semi-rhythmic involuntary contractions of muscle groups supplied by one or more contiguous segments of the brainstem and/or spinal cord....\n --PARENT--> [8A06] Myoclonic disorders\n --EXCLUDES--> [?] 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...", "[8A06.1] Segmental myoclonus\n Def: Rhythmic or semi-rhythmic involuntary contractions of muscle groups supplied by one or more contiguous segments of the brainstem and/or spinal cord....\n --PARENT--> [8A06] Myoclonic disorders\n --PARENT--> [?] Movement disorders\n Def: This is a group of involuntary movement disorders....", "[EC23.0] Non-syndromic genetically-determined hypermelanosis or lentiginosis\n --PARENT--> [EC23] Genetic disorders of skin pigmentation\n Def: Genetic disorders of the skin characterised by disordered pigmentation, including albinism and inherited forms of lentiginosis....\n --PARENT--> [?] Genetic or developmental disorders affecting the skin\n Def: A large group of disorders, some limited to the skin but many involving other organ systems, due to heritable genetic defects, chromosomal abnormalities or embryofetal developmental anomalies....", "[EC23.0] Non-syndromic genetically-determined hypermelanosis or lentiginosis\n --PARENT--> [EC23] Genetic disorders of skin pigmentation\n Def: Genetic disorders of the skin characterised by disordered pigmentation, including albinism and inherited forms of lentiginosis....\n --CHILD--> [EC23.0] Non-syndromic genetically-determined hypermelanosis or lentiginosis" ]
ME93.0
Segmental and somatic dysfunction
[ { "from_icd11": "ME93.0", "icd10_code": "M9905", "icd10_title": "Segmental and somatic dysfunction of pelvic region" }, { "from_icd11": "ME93.0", "icd10_code": "M990", "icd10_title": "Segmental and somatic dysfunction" }, { "from_icd11": "EC23.0", "icd10_code": "L814", "icd10_title": "Other melanin hyperpigmentation" }, { "from_icd11": "EC23.0", "icd10_code": "L80-L99", "icd10_title": "" }, { "from_icd11": "EC23.0", "icd10_code": "L81", "icd10_title": "Other disorders of pigmentation" }, { "from_icd11": "EC23.0", "icd10_code": "L813", "icd10_title": "Cafe au lait spots" }, { "from_icd11": "BD51.Z", "icd10_code": "I728", "icd10_title": "Aneurysm of other specified arteries" }, { "from_icd11": "BD51.Z", "icd10_code": "I729", "icd10_title": "Aneurysm of unspecified site" }, { "from_icd11": "BD51.Z", "icd10_code": "I72", "icd10_title": "Other aneurysm" }, { "from_icd11": "BA81", "icd10_code": "I2542", "icd10_title": "Coronary artery dissection" }, { "from_icd11": "BA81", "icd10_code": "I2541", "icd10_title": "Coronary artery aneurysm" }, { "from_icd11": "BA81", "icd10_code": "I254", "icd10_title": "Coronary artery aneurysm and dissection" }, { "from_icd11": "BB02.1Z", "icd10_code": "I281", "icd10_title": "Aneurysm of pulmonary artery" }, { "from_icd11": "BD51.4", "icd10_code": "I722", "icd10_title": "Aneurysm of renal artery" } ]
M9905
Segmental and somatic dysfunction of pelvic region
Microscopic sections showed a micronodular appearance, composed of irregularly shaped vascular spaces lined by plump endothelial cells and surrounded by concentric collagen fibers, features in keeping with SANT (approved by immunohistochemistry) . All the resected lymph nodes showed reactive changes. In a follow-up visit a month later, the patient showed improvement in her symptoms, and the anemia resolved (hemoglobin concentration: 12 g/dl). All workups for short stature (biochemical assessments and radiological tests for estimating bone age) showed appropriate results, and after receiving treatment for allergic sinusitis, the puffy face disappeared. Additionally, no clinical or radiologic deficits were noted during the 10-month follow-up visits. Informed consent was requested and obtained from the patient for publishing the case report and the accompanying images. Fig. 3 Low-power section of the resected mass shows multiple variably sized angiomatoid nodules within the red pulp separated by fibrosclerotic septa [hematoxylin and eosin (H&E) × 100] ( A ). The nodules are composed of well-formed capillaries arranged in a lobular pattern, sinusoid-like spaces, inflammatory cells, and histiocytes. There is no cellular atypia or necrosis (H&E × 200) ( B ) Fig. 4 The immunostaining of the resected mass revealed three distinct kinds of vessels in the angiomatoid nodules positive for CD31, CD34, and CD8
4.042969
0.859863
sec[1]/p[2]
en
0.999995
37735700
https://doi.org/10.1186/s13256-023-04144-0
[ "resected", "nodules", "composed", "spaces", "cells", "angiomatoid", "microscopic", "sections", "micronodular", "appearance" ]
[ { "code": "2E88", "title": "Benign endometrial stromal nodule" }, { "code": "FA20.0", "title": "Seropositive rheumatoid arthritis" }, { "code": "1F20.Z", "title": "Aspergillosis, unspecified" }, { "code": "MF30", "title": "Breast lump or mass female" }, { "code": "5A01.1", "title": "Nontoxic single thyroid nodule" }, { "code": "QD71.1", "title": "Inadequate housing" }, { "code": "PA50.Z", "title": "Unintentional air or space transport injury event, unspecified" }, { "code": "AB32.0", "title": "Persistent Postural-Perceptual Dizziness" }, { "code": "DA0E.3", "title": "Anomalies of tooth position" }, { "code": "NC90.Z", "title": "Superficial injury of knee or lower leg, unspecified" } ]
=== ICD-11 CODES FOUND === [2E88] Benign endometrial stromal nodule Also known as: Benign endometrial stromal nodule | benign endometrial stromal tumour | Endometrial node | Stromal nodule [FA20.0] Seropositive rheumatoid arthritis Also known as: Seropositive rheumatoid arthritis | high positive rheumatoid factor | low positive rheumatoid factor | high positive anticitrullinated protein antibody | low positive anticitrullinated protein antibody [1F20.Z] Aspergillosis, unspecified Also known as: Aspergillosis, unspecified | Aspergillosis | aspergilloma | aspergillus nodule | simple aspergilloma [MF30] Breast lump or mass female Also known as: Breast lump or mass female | breast irregular nodularity | breast node | lump in breast | lump or mass in breast NOS [5A01.1] Nontoxic single thyroid nodule Definition: Single tumour of the thyroid gland due to follicular multiplication, unaccompanied by hyperthyroidism or thyrotoxicosis Also known as: Nontoxic single thyroid nodule | colloid goitre (in part) | follicular goitre | struma follicularis | parenchymatous goitre [QD71.1] Inadequate housing Also known as: Inadequate housing | lack of adequate housing | problem with inadequate housing | restriction of housing space | unsatisfactory surroundings Excludes: Problems associated with the natural environment or human-made changes to the environment [PA50.Z] Unintentional air or space transport injury event, unspecified Also known as: Unintentional air or space transport injury event, unspecified | Unintentional air or space transport injury event | Air and space transport accidents | Air transport accident NOS | Aircraft accident NOS [AB32.0] Persistent Postural-Perceptual Dizziness Definition: Persistent non-vertiginous dizziness, unsteadiness, or both lasting three months or more. Symptoms are present most days, often increasing throughout the day, but may wax and wane. Momentary flares may occur spontaneously or with sudden movement. Affected individuals feel worst when upright, exposed to moving or complex visual stimuli, and during active or passive head motion. These situations may not be equally provocative. Typically, the disorder follows occurrences of acute or episodic vestib Also known as: Persistent Postural-Perceptual Dizziness | Chronic subjective dizziness | Phobic postural vertigo | Visual vertigo | Space and motion discomfort [DA0E.3] Anomalies of tooth position Definition: Dental anomalies are craniofacial abnormalities of form, function, or position of the teeth, bones, and tissues of the jaw and mouth. Anomalies of tooth position can be classified in ectopic, transmigration, transposition, rotation. Also known as: Anomalies of tooth position | Diastema of teeth | abnormal spacing of tooth or teeth | Crowding of tooth or teeth | Distomolar causing crowding Includes: Diastema of teeth [NC90.Z] Superficial injury of knee or lower leg, unspecified Also known as: Superficial injury of knee or lower leg, unspecified | Superficial injury of knee or lower leg | Superficial injury of knee | Superficial injury of popliteal space === GRAPH WALKS === --- Walk 1 --- [2E88] Benign endometrial stromal nodule --PARENT--> [?] Benign mesenchymal neoplasms Def: Bening neoplasms of muscle, fat, fibrous tissue, bone, cartilage, and blood vessels.... --CHILD--> [2E80] Benign lipomatous neoplasm Def: A benign tumour composed of adipose (fatty) tissue. The most common representative of this category is the lipoma.... --- Walk 2 --- [2E88] Benign endometrial stromal nodule --PARENT--> [?] Benign mesenchymal neoplasms Def: Bening neoplasms of muscle, fat, fibrous tissue, bone, cartilage, and blood vessels.... --CHILD--> [2E80] Benign lipomatous neoplasm Def: A benign tumour composed of adipose (fatty) tissue. The most common representative of this category is the lipoma.... --- Walk 3 --- [FA20.0] Seropositive rheumatoid arthritis --PARENT--> [FA20] Rheumatoid arthritis Def: Rheumatoid arthritis (RA) is persistent and/or erosive disease that is defined as the confirmed presence of synovitis in at least 1 joint, absence of an alternative diagnosis that better explains the ... --CHILD--> [FA20.0] Seropositive rheumatoid arthritis --- Walk 4 --- [FA20.0] Seropositive rheumatoid arthritis --PARENT--> [FA20] Rheumatoid arthritis Def: Rheumatoid arthritis (RA) is persistent and/or erosive disease that is defined as the confirmed presence of synovitis in at least 1 joint, absence of an alternative diagnosis that better explains the ... --EXCLUDES--> [?] Acute rheumatic fever Def: A disease of the connective tissue, caused by an infection with the gram-positive bacteria Streptococcus pyogenes (the disease may also affect the heart, joints, central nervous system, subcutaneous t... --- Walk 5 --- [1F20.Z] Aspergillosis, unspecified --PARENT--> [1F20] Aspergillosis Def: Aspergillosis is a disease caused by fungi of the genus Aspergillus. The organism is ubiquitous, being found in soil and water or in decaying vegetation. While Aspergillus is entirely harmless for mos... --CHILD--> [1F20.1] Non-invasive aspergillosis --- Walk 6 --- [1F20.Z] Aspergillosis, unspecified --PARENT--> [1F20] Aspergillosis Def: Aspergillosis is a disease caused by fungi of the genus Aspergillus. The organism is ubiquitous, being found in soil and water or in decaying vegetation. While Aspergillus is entirely harmless for mos... --RELATED_TO--> [?] Aspergillus-induced allergic or hypersensitivity conditions
[ "[2E88] Benign endometrial stromal nodule\n --PARENT--> [?] Benign mesenchymal neoplasms\n Def: Bening neoplasms of muscle, fat, fibrous tissue, bone, cartilage, and blood vessels....\n --CHILD--> [2E80] Benign lipomatous neoplasm\n Def: A benign tumour composed of adipose (fatty) tissue. The most common representative of this category is the lipoma....", "[2E88] Benign endometrial stromal nodule\n --PARENT--> [?] Benign mesenchymal neoplasms\n Def: Bening neoplasms of muscle, fat, fibrous tissue, bone, cartilage, and blood vessels....\n --CHILD--> [2E80] Benign lipomatous neoplasm\n Def: A benign tumour composed of adipose (fatty) tissue. The most common representative of this category is the lipoma....", "[FA20.0] Seropositive rheumatoid arthritis\n --PARENT--> [FA20] Rheumatoid arthritis\n Def: Rheumatoid arthritis (RA) is persistent and/or erosive disease that is defined as the confirmed presence of synovitis in at least 1 joint, absence of an alternative diagnosis that better explains the ...\n --CHILD--> [FA20.0] Seropositive rheumatoid arthritis", "[FA20.0] Seropositive rheumatoid arthritis\n --PARENT--> [FA20] Rheumatoid arthritis\n Def: Rheumatoid arthritis (RA) is persistent and/or erosive disease that is defined as the confirmed presence of synovitis in at least 1 joint, absence of an alternative diagnosis that better explains the ...\n --EXCLUDES--> [?] Acute rheumatic fever\n Def: A disease of the connective tissue, caused by an infection with the gram-positive bacteria Streptococcus pyogenes (the disease may also affect the heart, joints, central nervous system, subcutaneous t...", "[1F20.Z] Aspergillosis, unspecified\n --PARENT--> [1F20] Aspergillosis\n Def: Aspergillosis is a disease caused by fungi of the genus Aspergillus. The organism is ubiquitous, being found in soil and water or in decaying vegetation. While Aspergillus is entirely harmless for mos...\n --CHILD--> [1F20.1] Non-invasive aspergillosis", "[1F20.Z] Aspergillosis, unspecified\n --PARENT--> [1F20] Aspergillosis\n Def: Aspergillosis is a disease caused by fungi of the genus Aspergillus. The organism is ubiquitous, being found in soil and water or in decaying vegetation. While Aspergillus is entirely harmless for mos...\n --RELATED_TO--> [?] Aspergillus-induced allergic or hypersensitivity conditions" ]
2E88
Benign endometrial stromal nodule
[ { "from_icd11": "FA20.0", "icd10_code": "M0569", "icd10_title": "Rheumatoid arthritis of multiple sites with involvement of other organs and systems" }, { "from_icd11": "FA20.0", "icd10_code": "M0579", "icd10_title": "Rheumatoid arthritis with rheumatoid factor of multiple sites without organ or systems involvement" }, { "from_icd11": "FA20.0", "icd10_code": "M05612", "icd10_title": "Rheumatoid arthritis of left shoulder with involvement of other organs and systems" }, { "from_icd11": "FA20.0", "icd10_code": "M0570", "icd10_title": "Rheumatoid arthritis with rheumatoid factor of unspecified site without organ or systems involvement" }, { "from_icd11": "FA20.0", "icd10_code": "M0560", "icd10_title": "Rheumatoid arthritis of unspecified site with involvement of other organs and systems" }, { "from_icd11": "FA20.0", "icd10_code": "M0500", "icd10_title": "Felty's syndrome, unspecified site" }, { "from_icd11": "FA20.0", "icd10_code": "M0639", "icd10_title": "Rheumatoid nodule, multiple sites" }, { "from_icd11": "FA20.0", "icd10_code": "M0630", "icd10_title": "Rheumatoid nodule, unspecified site" }, { "from_icd11": "FA20.0", "icd10_code": "M05", "icd10_title": "Rheumatoid arthritis with rheumatoid factor" }, { "from_icd11": "FA20.0", "icd10_code": "M050", "icd10_title": "Felty's syndrome" }, { "from_icd11": "FA20.0", "icd10_code": "M063", "icd10_title": "Rheumatoid nodule" }, { "from_icd11": "1F20.Z", "icd10_code": "B4489", "icd10_title": "Other forms of aspergillosis" }, { "from_icd11": "1F20.Z", "icd10_code": "B4481", "icd10_title": "Allergic bronchopulmonary aspergillosis" }, { "from_icd11": "1F20.Z", "icd10_code": "B441", "icd10_title": "Other pulmonary aspergillosis" }, { "from_icd11": "1F20.Z", "icd10_code": "B449", "icd10_title": "Aspergillosis, unspecified" } ]
M0569
Rheumatoid arthritis of multiple sites with involvement of other organs and systems
This case presents a 36-year-old female patient who sought treatment for her maxillary left first premolar in the Department of Periodontology, School of Dentistry at Aracatuba, UNESP. She presented with a ceramic crown on tooth 24, and her main complaint was excessive tooth mobility, pain during mastication, tooth fragility, and bleeding during chewing or even spontaneously bleeding. Her medical history was unremarkable, and she denied use of alcohol or smoke and medications. The clinical examination showed endodontic treatment, signs of class I tooth mobility, and a ceramic crown ( Figure 1(A) ). During periodontal probing, it was verified 10 mm of probing depth in the buccal side ( Figure 1(B) ). Her periodontal biotype was classified as thick, with a sufficient amount of keratinized gingiva. Periapical radiograph revealed an inadequate endodontic treatment, vertical bone loss on the mesial, and distal side of the tooth, and the reminiscent bone height above the root apex was 10 mm ( Figure 1(C) ). After removing the prosthesis, it noted a vertical fracture in the mesial side of the teeth, which indicates its extraction ( Figure 1(D) ). The treatment proposed to the patient was the IDR technique with simultaneous regenerative procedure, dental implant placement, and prosthesis provisionalization in a one-stage approach. The patient signed an informed consent authorizing the proposed treatment.
3.890625
0.983887
sec[1]/p[0]
en
0.999998
PMC10874294
https://doi.org/10.1155/2024/5862595
[ "tooth", "side", "ceramic", "crown", "mobility", "bleeding", "endodontic", "periodontal", "probing", "vertical" ]
[ { "code": "DA07.6Y", "title": "Other specified disturbances in tooth eruption" }, { "code": "LA30.0", "title": "Anodontia" }, { "code": "QA00.8", "title": "Dental examination" }, { "code": "LA30.3", "title": "Hyperdontia" }, { "code": "DA0A.Y", "title": "Other specified disorders of teeth and supporting structures" }, { "code": "NE60", "title": "Harmful effects of drugs, medicaments or biological substances, not elsewhere classified" }, { "code": "LA8B.2Y", "title": "Other specified congenital anomaly of aorta or its branches" }, { "code": "LB9A.6", "title": "Split foot" }, { "code": "LA80.0", "title": "Laevocardia" }, { "code": "LA80.1", "title": "Dextrocardia" } ]
=== ICD-11 CODES FOUND === [DA07.6Y] Other specified disturbances in tooth eruption Also known as: Other specified disturbances in tooth eruption | Neonatal teeth | Natal teeth | Advanced tooth eruption | precocious dentition Includes: Neonatal teeth | Advanced tooth eruption [LA30.0] Anodontia Definition: Anodontia is a genetic disorder commonly defined as the absence of all teeth, affecting both temporary and permanent dentitions, and is extremely rarely encountered in a pure form without any associated abnormalities. Rare but more common than complete anodontia is hypodontia. Also known as: Anodontia | agomphiasis | agomphosis | anodontism | complete absence of teeth [QA00.8] Dental examination Also known as: Dental examination | examination of teeth [LA30.3] Hyperdontia Definition: Hyperdontia is the condition of having supernumerary teeth, or teeth which appear in addition to the regular number of teeth. Also known as: Hyperdontia | Supplementary teeth | Supernumerary teeth | supernumerary tooth | supplemental teeth Includes: Supplementary teeth | Supernumerary teeth | distomolar [DA0A.Y] Other specified disorders of teeth and supporting structures Also known as: Other specified disorders of teeth and supporting structures | Alveolar process haemorrhage | alveolar haemorrhage | Barodontalgia | aerodontalgia [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 [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 [LB9A.6] Split foot Definition: A condition caused by malformation of the foot during the antenatal period. This condition is characterised by a deep median cleft of the foot due to the absence of the central rays. Also known as: Split foot | lobster claw foot | split foot, unspecified side | cleft of foot | Split foot, unilateral [LA80.0] Laevocardia Definition: A congenital cardiovascular finding in which the heart is predominantly to the left of the thoracic midline. Also known as: Laevocardia | Left-sided heart | Levocardia [LA80.1] Dextrocardia Definition: A congenital cardiovascular malformation in which the heart is predominantly to the right of the thoracic midline. This is independent of the orientation of the cardiac apex. Also known as: Dextrocardia | heart in right chest | right-sided heart | congenital dextrocardia of heart | transposition of heart Excludes: Isomerism of left atrial appendages | Isomerism of right atrial appendages | Total mirror imagery === GRAPH WALKS === --- Walk 1 --- [DA07.6Y] Other specified disturbances in tooth eruption --PARENT--> [DA07.6] Disturbances in tooth eruption --PARENT--> [DA07] Disorders of tooth development or eruption Def: Alteration of the normal formation process of the tooth, the normal chronology of eruption into the mouth or the proper alignment in the dental arch affecting a single or multiple teeth.... --- Walk 2 --- [DA07.6Y] Other specified disturbances in tooth eruption --PARENT--> [DA07.6] Disturbances in tooth eruption --CHILD--> [DA07.60] Teething syndrome Def: Gum and jaw discomfort when an infant’s teeth emerges. Teething typically starts between 4 and 7 months of age and lasts until about the age of 3 years. Most common symptoms include irritability, cryi... --- Walk 3 --- [LA30.0] Anodontia Def: Anodontia is a genetic disorder commonly defined as the absence of all teeth, affecting both temporary and permanent dentitions, and is extremely rarely encountered in a pure form without any associat... --PARENT--> [LA30] Structural developmental anomalies of teeth and periodontal tissues --CHILD--> [LA30.0] Anodontia Def: Anodontia is a genetic disorder commonly defined as the absence of all teeth, affecting both temporary and permanent dentitions, and is extremely rarely encountered in a pure form without any associat... --- Walk 4 --- [LA30.0] Anodontia Def: Anodontia is a genetic disorder commonly defined as the absence of all teeth, affecting both temporary and permanent dentitions, and is extremely rarely encountered in a pure form without any associat... --PARENT--> [LA30] Structural developmental anomalies of teeth and periodontal tissues --RELATED_TO--> [?] Root anomaly Def: Common presence of fused roots showed by X-ray film that short or long root, supernumerary root, or fused roots. These root anomalies are commonly seen in permanent molars, especially in third molars ... --- Walk 5 --- [QA00.8] Dental examination --PARENT--> [QA00] General examination or investigation of persons without complaint or reported diagnosis --CHILD--> [QA00.0] General adult medical examination Def: Encounter for periodic examination (annual) (physical) and any associated laboratory and radiologic examinations on adult.... --- 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
[ "[DA07.6Y] Other specified disturbances in tooth eruption\n --PARENT--> [DA07.6] Disturbances in tooth eruption\n --PARENT--> [DA07] Disorders of tooth development or eruption\n Def: Alteration of the normal formation process of the tooth, the normal chronology of eruption into the mouth or the proper alignment in the dental arch affecting a single or multiple teeth....", "[DA07.6Y] Other specified disturbances in tooth eruption\n --PARENT--> [DA07.6] Disturbances in tooth eruption\n --CHILD--> [DA07.60] Teething syndrome\n Def: Gum and jaw discomfort when an infant’s teeth emerges. Teething typically starts between 4 and 7 months of age and lasts until about the age of 3 years. Most common symptoms include irritability, cryi...", "[LA30.0] Anodontia\n Def: Anodontia is a genetic disorder commonly defined as the absence of all teeth, affecting both temporary and permanent dentitions, and is extremely rarely encountered in a pure form without any associat...\n --PARENT--> [LA30] Structural developmental anomalies of teeth and periodontal tissues\n --CHILD--> [LA30.0] Anodontia\n Def: Anodontia is a genetic disorder commonly defined as the absence of all teeth, affecting both temporary and permanent dentitions, and is extremely rarely encountered in a pure form without any associat...", "[LA30.0] Anodontia\n Def: Anodontia is a genetic disorder commonly defined as the absence of all teeth, affecting both temporary and permanent dentitions, and is extremely rarely encountered in a pure form without any associat...\n --PARENT--> [LA30] Structural developmental anomalies of teeth and periodontal tissues\n --RELATED_TO--> [?] Root anomaly\n Def: Common presence of fused roots showed by X-ray film that short or long root, supernumerary root, or fused roots. These root anomalies are commonly seen in permanent molars, especially in third molars ...", "[QA00.8] Dental examination\n --PARENT--> [QA00] General examination or investigation of persons without complaint or reported diagnosis\n --CHILD--> [QA00.0] General adult medical examination\n Def: Encounter for periodic examination (annual) (physical) and any associated laboratory and radiologic examinations on adult....", "[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" ]
DA07.6Y
Other specified disturbances in tooth eruption
[ { "from_icd11": "LA30.0", "icd10_code": "K000", "icd10_title": "Anodontia" }, { "from_icd11": "QA00.8", "icd10_code": "Z012", "icd10_title": "Encounter for dental examination and cleaning" }, { "from_icd11": "LA30.3", "icd10_code": "K001", "icd10_title": "Supernumerary teeth" }, { "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" } ]
K000
Anodontia
Immune checkpoint inhibitors (ICIs) are a class of immunotherapy agents that have revolutionized cancer treatment by enhancing the immune system's ability to recognize and attack cancer cells. They are a class of monoclonal antibodies that target host immune negative regulation receptors, such as CTLA‐4 (cytotoxic T‐lymphocyte-associated protein 4), programmed cell death receptor 1 (PD‐1), and programmed cell death ligand 1 (PD‐L1) . Some of the US Food and Drug Administration-approved ICIs include ipilimumab (anti-CTLA-4), nivolumab, pembrolizumab, cemiplimab (anti-PD-1), avelumab, atezolizumab, and durvalumab (anti-PD-L1). With ICI therapy becoming more prevalent, we have started to notice many immune-related adverse events. ICIs break the balance of the body's immune system and reduce T-cell tolerance, thereby leading to the production of a series of adverse events. . These affect various organ systems in the body, including the skin, digestive, endocrine, respiratory, hematological, renal, and rarely the nervous and cardiovascular systems. Cardiac toxicities are rare and can range from pericarditis causing pericardial effusion to myocarditis and even severe fatal heart failure . Symptoms can present from shortly after initiation to several months after discontinuation. We report the case of pembrolizumab-induced myocarditis presenting as heart failure in a patient with colonic adenocarcinoma.
4.222656
0.817871
sec[0]/p[0]
en
0.999997
38883125
https://doi.org/10.7759/cureus.60459
[ "immune", "icis", "cell", "anti", "class", "that", "cancer", "system", "ctla", "programmed" ]
[ { "code": "4B4Z", "title": "Diseases of the immune system, unspecified" }, { "code": "4A01.1Z", "title": "Combined immunodeficiencies, unspecified" }, { "code": "4B4Y", "title": "Other specified diseases of the immune system" }, { "code": "1C62.3Z", "title": "HIV disease clinical stage 4 without mention of tuberculosis or malaria, unspecified" }, { "code": "4B2Y", "title": "Other specified disorders involving the immune system" }, { "code": "MF9Y", "title": "Other specified clinical findings on examination of urine, without diagnosis" }, { "code": "5C56.20", "title": "Mucolipidosis" }, { "code": "3A51.1", "title": "Sickle cell disease without crisis" }, { "code": "9A96.3", "title": "Primary anterior uveitis" }, { "code": "3A61.Z", "title": "Acquired pure red cell aplasia, unspecified" } ]
=== ICD-11 CODES FOUND === [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 [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 [4B4Y] Other specified diseases of the immune system Also known as: Other specified diseases of the immune system | Immunodeficiencies | Biotin-dependent carboxylase deficiency [1C62.3Z] HIV disease clinical stage 4 without mention of tuberculosis or malaria, unspecified Also known as: HIV disease clinical stage 4 without mention of tuberculosis or malaria, unspecified | HIV disease clinical stage 4 without mention of tuberculosis or malaria | HIV disease clinical stage 4 without tuberculosis or malaria | Acquired Immune Deficiency Syndrome | AIDS - [acquired immunodeficiency syndrome] [4B2Y] Other specified disorders involving the immune system Also known as: Other specified disorders involving the immune system | Certain inflammatory disorders with predominant lymph node involvement | Histiocytic necrotising lymphadenitis of Kikuchi and Fujimoto | Kikuchi-Fujimoto disease | Kimura disease [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) [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] [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 === GRAPH WALKS === --- Walk 1 --- [4B4Z] Diseases of the immune system, unspecified --PARENT--> [04] Diseases of the immune system --CHILD--> [?] Nonorgan specific systemic autoimmune disorders --- Walk 2 --- [4B4Z] Diseases of the immune system, unspecified --PARENT--> [04] Diseases of the immune system --EXCLUDES--> [?] Developmental anomalies Def: This chapter includes conditions caused by failure of a particular body site or body system to develop correctly during the antenatal period.... --- Walk 3 --- [4A01.1Z] Combined immunodeficiencies, unspecified --PARENT--> [4A01.1] Combined immunodeficiencies --CHILD--> [4A01.12] Major histocompatibility complex class II deficiency Def: Immunodeficiency by defective expression of HLA class II is an autosomal recessive primary immune deficiency, manifesting by recurrent viral and bacterial infections, often leading to chronic diarrhoe... --- Walk 4 --- [4A01.1Z] Combined immunodeficiencies, unspecified --PARENT--> [4A01.1] Combined immunodeficiencies --CHILD--> [4A01.10] Severe combined immunodeficiencies Def: Severe combined immunodeficiency (SCID) comprises a group of rare monogenic primary immunodeficiency disorders characterised by a lack of functional peripheral T lymphocytes resulting in early-onset s... --- Walk 5 --- [4B4Y] Other specified diseases of the immune system --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 --- [4B4Y] Other specified diseases of the immune system --PARENT--> [04] Diseases of the immune system --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 ...
[ "[4B4Z] Diseases of the immune system, unspecified\n --PARENT--> [04] Diseases of the immune system\n --CHILD--> [?] Nonorgan specific systemic autoimmune disorders", "[4B4Z] Diseases of the immune system, unspecified\n --PARENT--> [04] Diseases of the immune system\n --EXCLUDES--> [?] Developmental anomalies\n Def: This chapter includes conditions caused by failure of a particular body site or body system to develop correctly during the antenatal period....", "[4A01.1Z] Combined immunodeficiencies, unspecified\n --PARENT--> [4A01.1] Combined immunodeficiencies\n --CHILD--> [4A01.12] Major histocompatibility complex class II deficiency\n Def: Immunodeficiency by defective expression of HLA class II is an autosomal recessive primary immune deficiency, manifesting by recurrent viral and bacterial infections, often leading to chronic diarrhoe...", "[4A01.1Z] Combined immunodeficiencies, unspecified\n --PARENT--> [4A01.1] Combined immunodeficiencies\n --CHILD--> [4A01.10] Severe combined immunodeficiencies\n Def: Severe combined immunodeficiency (SCID) comprises a group of rare monogenic primary immunodeficiency disorders characterised by a lack of functional peripheral T lymphocytes resulting in early-onset s...", "[4B4Y] Other specified diseases of the immune system\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", "[4B4Y] Other specified diseases of the immune system\n --PARENT--> [04] Diseases of the immune system\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 ..." ]
4B4Z
Diseases of the immune system, unspecified
[ { "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": "D848", "icd10_title": "Other specified immunodeficiencies" }, { "from_icd11": "4B4Z", "icd10_code": "D899", "icd10_title": "Disorder involving the immune mechanism, unspecified" }, { "from_icd11": "4B4Z", "icd10_code": "D80-D89", "icd10_title": "" }, { "from_icd11": "4B4Z", "icd10_code": "D84", "icd10_title": "Other immunodeficiencies" } ]
D8940
Mast cell activation, unspecified
A 43-year-old African American male with a past medical history of type II diabetes mellitus, dyslipidemia, non-alcoholic steatohepatitis, major depressive disorder, and tobacco dependence was hospitalized after a suicide attempt by ingestion of 480,000 mg of metformin. He presented with altered mental status and continuous vomiting. Initial vital signs showed a blood pressure of 90/52 mmHg, pulse rate of 50 beats per minute (bpm), respiratory rate of 40 breaths per minute. His point of care glucose was 100 mg/dL. He received several isotonic intravenous fluid boluses with 0.9% saline, was intubated for airway support, and received activated charcoal and polyethylene glycol via a nasogastric tube. The initial serum potassium was 4.9 mmol/L, blood urea nitrogen (BUN) was 10 mg/dL, creatinine was 1.2 mg/dL, bicarbonate (HCO 3 ) was 16 mmol/L, anion gap was 22, serum lactate was 6.6 mmol/L, and arterial pH was 7.16. Labs 4 hours later showed serum potassium of 7.4 mmol/L, HCO 3 of 12 mmol/L, and lactate of 11.8 mmol/L. Given the amount of ingestion, worsening lactic acidosis, and hyperkalemia, emergent high flux hemodialysis (HFHD) was initiated with an Optiflux 200 (Fresenius Medical Care, Waltham, MA, USA) on a Gambro Phoenix Hemodialysis System (Gambro, Deerfield, IL, USA) with a blood flow of 450 mL/minute, dialysate flow of 500 mL/minute, potassium 1.0 bath, and a bicarbonate bath of 36 mmol/L.
3.943359
0.970215
sec[1]/p[0]
en
0.999996
37858266
https://doi.org/10.1186/s13256-023-04201-8
[ "mmol", "minute", "blood", "serum", "potassium", "ingestion", "bicarbonate", "lactate", "hemodialysis", "gambro" ]
[ { "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": "ED5Y", "title": "Other specified disorders of epidermal keratinisation" }, { "code": "KD30.0", "title": "Birth depression with 5 minute Apgar score 0-3" }, { "code": "KD30.1", "title": "Birth depression with 5 minute Apgar score 4-6" }, { "code": "KB21.0", "title": "Severe birth asphyxia" }, { "code": "KB21.1", "title": "Mild and moderate birth asphyxia" }, { "code": "3C0Z", "title": "Diseases of the blood or blood-forming organs, unspecified" }, { "code": "MF50.4Z", "title": "Haematuria, unspecified" } ]
=== ICD-11 CODES FOUND === [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 [ED5Y] Other specified disorders of epidermal keratinisation Also known as: Other specified disorders of epidermal keratinisation | Follicular digitate keratoses | Lichen spinulosus | Keratosis spinulosa | Keratosis circumscripta [KD30.0] Birth depression with 5 minute Apgar score 0-3 Definition: A condition characterised by cardiorespiratory and neurological depression, defined as an Apgar score between 0 to 3 at 5 minutes following birth. Also known as: Birth depression with 5 minute Apgar score 0-3 [KD30.1] Birth depression with 5 minute Apgar score 4-6 Definition: A condition characterised by cardiorespiratory and neurological depression, defined as an Apgar score between 4 and 6 at 5 minutes following birth. Also known as: Birth depression with 5 minute Apgar score 4-6 [KB21.0] Severe birth asphyxia Definition: Pulse less than 100 per minute at birth and falling or steady, respiration absent or gasping, colour poor, tone absent. Also known as: Severe birth asphyxia | severe perinatal hypoxia | asphyxia pallida of newborn | Asphyxia with 5-minute Apgar score 0-3 | newborn severe asphyxia [KB21.1] Mild and moderate birth asphyxia Definition: Normal respiration not established within one minute, but heart rate 100 or above, some muscle tone present, some response to stimulation. Also known as: Mild and moderate birth asphyxia | asphyxia livida of newborn | Asphyxia with 5-minute Apgar score 4-7 | Blue asphyxia [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 --- [GB42.1] Albuminuria, Grade A3 Def: 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... --PARENT--> [GB42] 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... --EXCLUDES--> [?] 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 2 --- [GB42.1] Albuminuria, Grade A3 Def: 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... --PARENT--> [GB42] 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... --EXCLUDES--> [?] 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... --- Walk 3 --- [GB42.0] Albuminuria, Grade A2 Def: 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... --PARENT--> [GB42] 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... --CHILD--> [GB42.1] Albuminuria, Grade A3 Def: 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... --- Walk 4 --- [GB42.0] Albuminuria, Grade A2 Def: 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... --PARENT--> [GB42] 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... --CHILD--> [GB42.0] Albuminuria, Grade A2 Def: 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... --- Walk 5 --- [MA18.0Y] Other specified elevated blood glucose level --PARENT--> [MA18.0] Elevated blood glucose level --CHILD--> [MA18.00] Abnormal glucose tolerance test Def: Greater than normal levels of glucose found in laboratory examination of the blood to check how the body breaks down (metabolizes) blood sugar. Positive findings may indicate diabetes or Cushing disea... --- Walk 6 --- [MA18.0Y] Other specified elevated blood glucose level --PARENT--> [MA18.0] Elevated blood glucose level --CHILD--> [MA18.00] Abnormal glucose tolerance test Def: Greater than normal levels of glucose found in laboratory examination of the blood to check how the body breaks down (metabolizes) blood sugar. Positive findings may indicate diabetes or Cushing disea...
[ "[GB42.1] Albuminuria, Grade A3\n Def: 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...\n --PARENT--> [GB42] 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...\n --EXCLUDES--> [?] 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....", "[GB42.1] Albuminuria, Grade A3\n Def: 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...\n --PARENT--> [GB42] 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...\n --EXCLUDES--> [?] 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...", "[GB42.0] Albuminuria, Grade A2\n Def: 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...\n --PARENT--> [GB42] 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...\n --CHILD--> [GB42.1] Albuminuria, Grade A3\n Def: 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...", "[GB42.0] Albuminuria, Grade A2\n Def: 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...\n --PARENT--> [GB42] 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...\n --CHILD--> [GB42.0] Albuminuria, Grade A2\n Def: 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...", "[MA18.0Y] Other specified elevated blood glucose level\n --PARENT--> [MA18.0] Elevated blood glucose level\n --CHILD--> [MA18.00] Abnormal glucose tolerance test\n Def: Greater than normal levels of glucose found in laboratory examination of the blood to check how the body breaks down (metabolizes) blood sugar. Positive findings may indicate diabetes or Cushing disea...", "[MA18.0Y] Other specified elevated blood glucose level\n --PARENT--> [MA18.0] Elevated blood glucose level\n --CHILD--> [MA18.00] Abnormal glucose tolerance test\n Def: Greater than normal levels of glucose found in laboratory examination of the blood to check how the body breaks down (metabolizes) blood sugar. Positive findings may indicate diabetes or Cushing disea..." ]
GB42.1
Albuminuria, Grade A3
[ { "from_icd11": "KD30.0", "icd10_code": "P210", "icd10_title": "" }, { "from_icd11": "KD30.1", "icd10_code": "P211", "icd10_title": "" }, { "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" } ]
P210
Cosyntropin stimulation test revealed an intact adrenal response. Recent infection in the setting of acute blood loss anemia, hypotension, and hyperkalemia prompted concern for secondary adrenal insufficiency, and an MRI was ordered to rule out a pituitary adenoma, but the patient suffered from claustrophobia and the imaging study was not successfully done. Nephrology initiated a sodium bicarbonate infusion and was also considering hemodialysis if the potassium did not improve the next day, as by now it had reached a peak of 6.5 mEq/L . Electrocardiograms persistently revealed normal sinus rhythm and no segmental or wave abnormalities . Intravenous hydrocortisone at 100 mg every eight hours was started per endocrinology, and by the next day, the hyperkalemia resolved, and her creatinine returned to baseline in the next 48 hours. The sodium bicarbonate infusion was discontinued, and the hydrocortisone was tapered down gradually to intravenous 50 mg twice a day, followed by 25 mg twice a day, and then an oral regimen for a total of four days. Wound cultures from the hip irrigation returned positive for methicillin-resistant Staphylococcus aureus (MRSA), and the patient was discharged and completed a one-month course of IV daptomycin at a short-stay unit. The patient received follow-up labs one month later, including adrenal labs that included ACTH and random cortisol that were within normal limits.
3.822266
0.976074
sec[1]/p[2]
en
0.999996
PMC10557372
https://doi.org/10.7759/cureus.44770
[ "adrenal", "next", "hyperkalemia", "sodium", "bicarbonate", "infusion", "intravenous", "hydrocortisone", "hours", "returned" ]
[ { "code": "5A76.Y", "title": "Other specified disorders of adrenal gland" }, { "code": "5A7Z", "title": "Disorders of the adrenal glands or adrenal hormone system, unspecified" }, { "code": "5A74.Z", "title": "Adrenocortical insufficiency, unspecified" }, { "code": "5A74.Y", "title": "Other specified adrenocortical insufficiency" }, { "code": "LC8Z", "title": "Structural developmental anomalies of the adrenal glands, unspecified" }, { "code": "NE85.6", "title": "Other or unspecified complications of amputation stump" }, { "code": "5C76", "title": "Hyperkalaemia" }, { "code": "KB63.31", "title": "Hyperkalaemia of newborn" }, { "code": "3A10.3", "title": "Familial pseudohyperkalaemia" }, { "code": "5C72", "title": "Hypo-osmolality or hyponatraemia" } ]
=== ICD-11 CODES FOUND === [5A76.Y] Other specified disorders of adrenal gland Also known as: Other specified disorders of adrenal gland | Suprarenal gland abscess | Suprarenal abscess | Adrenal gland inflammation | adrenal glandular inflammation [5A7Z] Disorders of the adrenal glands or adrenal hormone system, unspecified Also known as: Disorders of the adrenal glands or adrenal hormone system, unspecified | Adrenal gland disease, not elsewhere classified | adrenal cortex disease | adrenal cortical disease | adrenal glandular disease [5A74.Z] Adrenocortical insufficiency, unspecified Also known as: Adrenocortical insufficiency, unspecified | Adrenocortical insufficiency | adrenal failure NOS | Hypoadrenocorticism | adrenocortical hypofunction [5A74.Y] Other specified adrenocortical insufficiency Also known as: Other specified adrenocortical insufficiency | Congenital adrenocortical insufficiency | Congenital isolated ACTH deficiency | Familial adrenal hypoplasia | Familial hypoadrenocorticism [LC8Z] Structural developmental anomalies of the adrenal glands, unspecified Also known as: Structural developmental anomalies of the adrenal glands, unspecified | adrenal anomaly | adrenal gland anomaly | congenital anomaly of adrenal gland | congenital malformation of adrenal gland [NE85.6] Other or unspecified complications of amputation stump Also known as: Other or unspecified complications of amputation stump | Abnormal or painful amputation stump | Amputation stump contracture | Amputation stump oedema | Oedema of amputation stump Excludes: Phantom limb syndrome [5C76] Hyperkalaemia Also known as: Hyperkalaemia | Potassium [K] excess | Potassium [K] overload | hyperaemic syndrome | hyperpotassaemia Includes: Potassium [K] excess | Potassium [K] overload [KB63.31] Hyperkalaemia of newborn Definition: Hyperkalaemia is defined as serum potassium greater than 5.5 mmol/L. Also known as: Hyperkalaemia of newborn [3A10.3] Familial pseudohyperkalaemia Definition: A disease caused by a genetically inherited mutation. This disease is characterised by a temperature-dependent defect in red cell membrane permeability to potassium that leads to high in vitro potassium levels in samples stored below 37°C leading to elevated potassium levels in the blood that does not reflect the true potassium level. Confirmation is by identification of genetic mutation through genetic testing. Also known as: Familial pseudohyperkalaemia | Hereditary pseudohyperkalaemia | Familial pseudohyperkalaemia type 1 | Familial pseudohyperkalaemia type 2 | Familial pseudohyperkalaemia, Cardiff type [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 === GRAPH WALKS === --- Walk 1 --- [5A76.Y] Other specified disorders of adrenal gland --PARENT--> [5A76] Certain specified disorders of adrenal gland --CHILD--> [5A76.Y] Other specified disorders of adrenal gland --- Walk 2 --- [5A76.Y] Other specified disorders of adrenal gland --PARENT--> [5A76] Certain specified disorders of adrenal gland --CHILD--> [5A76.Y] Other specified disorders of adrenal gland --- Walk 3 --- [5A7Z] Disorders of the adrenal glands or adrenal hormone system, unspecified --PARENT--> [?] Disorders of the adrenal glands or adrenal hormone system --RELATED_TO--> [?] 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).... --- Walk 4 --- [5A7Z] Disorders of the adrenal glands or adrenal hormone system, unspecified --PARENT--> [?] Disorders of the adrenal glands or adrenal hormone system --RELATED_TO--> [?] Growth hormone deficiency Def: Deficiency of growth hormone in children, adolescents and adults. Includes deficiency of growth hormone releasing hormone (GHRH) and excess of central somatostatin, leading to growth hormone deficienc... --- Walk 5 --- [5A74.Z] Adrenocortical insufficiency, unspecified --PARENT--> [5A74] Adrenocortical insufficiency Def: A condition in which the adrenal glands do not produce adequate amounts of steroid hormones, primarily cortisol. It may also include impaired production of aldosterone (a mineralocorticoid), which reg... --RELATED_TO--> [?] Neonatal haemorrhage originating in adrenal gland Def: A condition characterised by bleeding into the adrenal glands in a newborn.... --- Walk 6 --- [5A74.Z] Adrenocortical insufficiency, unspecified --PARENT--> [5A74] Adrenocortical insufficiency Def: A condition in which the adrenal glands do not produce adequate amounts of steroid hormones, primarily cortisol. It may also include impaired production of aldosterone (a mineralocorticoid), which reg... --CHILD--> [5A74.0] Acquired adrenocortical insufficiency Def: This is a acquired condition in which the adrenal glands do not produce adequate amounts of steroid hormones, primarily cortisol; but may also include impaired production of aldosterone (a mineralocor...
[ "[5A76.Y] Other specified disorders of adrenal gland\n --PARENT--> [5A76] Certain specified disorders of adrenal gland\n --CHILD--> [5A76.Y] Other specified disorders of adrenal gland", "[5A76.Y] Other specified disorders of adrenal gland\n --PARENT--> [5A76] Certain specified disorders of adrenal gland\n --CHILD--> [5A76.Y] Other specified disorders of adrenal gland", "[5A7Z] Disorders of the adrenal glands or adrenal hormone system, unspecified\n --PARENT--> [?] Disorders of the adrenal glands or adrenal hormone system\n --RELATED_TO--> [?] 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)....", "[5A7Z] Disorders of the adrenal glands or adrenal hormone system, unspecified\n --PARENT--> [?] Disorders of the adrenal glands or adrenal hormone system\n --RELATED_TO--> [?] Growth hormone deficiency\n Def: Deficiency of growth hormone in children, adolescents and adults. Includes deficiency of growth hormone releasing hormone (GHRH) and excess of central somatostatin, leading to growth hormone deficienc...", "[5A74.Z] Adrenocortical insufficiency, unspecified\n --PARENT--> [5A74] Adrenocortical insufficiency\n Def: A condition in which the adrenal glands do not produce adequate amounts of steroid hormones, primarily cortisol. It may also include impaired production of aldosterone (a mineralocorticoid), which reg...\n --RELATED_TO--> [?] Neonatal haemorrhage originating in adrenal gland\n Def: A condition characterised by bleeding into the adrenal glands in a newborn....", "[5A74.Z] Adrenocortical insufficiency, unspecified\n --PARENT--> [5A74] Adrenocortical insufficiency\n Def: A condition in which the adrenal glands do not produce adequate amounts of steroid hormones, primarily cortisol. It may also include impaired production of aldosterone (a mineralocorticoid), which reg...\n --CHILD--> [5A74.0] Acquired adrenocortical insufficiency\n Def: This is a acquired condition in which the adrenal glands do not produce adequate amounts of steroid hormones, primarily cortisol; but may also include impaired production of aldosterone (a mineralocor..." ]
5A76.Y
Other specified disorders of adrenal gland
[ { "from_icd11": "5A7Z", "icd10_code": "E2740", "icd10_title": "Unspecified adrenocortical insufficiency" }, { "from_icd11": "5A7Z", "icd10_code": "E2749", "icd10_title": "Other adrenocortical insufficiency" }, { "from_icd11": "5A7Z", "icd10_code": "E279", "icd10_title": "Disorder of adrenal gland, unspecified" }, { "from_icd11": "5A7Z", "icd10_code": "E27", "icd10_title": "Other disorders of adrenal gland" }, { "from_icd11": "5A7Z", "icd10_code": "E274", "icd10_title": "Other and unspecified adrenocortical insufficiency" }, { "from_icd11": "LC8Z", "icd10_code": "Q891", "icd10_title": "Congenital malformations of adrenal gland" }, { "from_icd11": "NE85.6", "icd10_code": "T8781", "icd10_title": "Dehiscence of amputation stump" }, { "from_icd11": "NE85.6", "icd10_code": "T8789", "icd10_title": "Other complications of amputation stump" }, { "from_icd11": "NE85.6", "icd10_code": "T876", "icd10_title": "" }, { "from_icd11": "5C76", "icd10_code": "E875", "icd10_title": "Hyperkalemia" }, { "from_icd11": "3A10.3", "icd10_code": "D588", "icd10_title": "Other specified hereditary hemolytic anemias" }, { "from_icd11": "5C72", "icd10_code": "E871", "icd10_title": "Hypo-osmolality and hyponatremia" } ]
E2740
Unspecified adrenocortical insufficiency
Curettage and saucerization of involved segment of mandible and total extraction of all teeth was done on the 2nd day of admission under general anaesthesia with nasotracheal intubation. Intraoperative findings revealed extensive necrosis of cortex and medullary bone and greenish discoloration of medullary portion of mandible suggestive of pseudomonas infection with multiple loose teeth. Swab from surgical site was sent for gram, acid-fast, and fungal staining with culture and sensitivity test. Necrotic tissue from the mandible was sent for histopathological examination. Patient was shifted to intensive care unit with endotracheal tube in situ. Postoperative course was uneventful for the rest of day. Extubation was done on the following day. Post-op days 2 to 4 were uneventful though she continued to have intermittent fever. Her blood and urine cultures sent on admission did not grow any organisms. Gram, Ziehl-Neelsen, and fungal staining of swab from surgical site revealed presence of few pus cells, plenty of gram-negative bacilli and few gram-positive cocci in pairs with no evidence of acid-fast bacilli or fungal elements. Culture from the swab grew multidrug resistant organism Morganella morganii ssp. morganii . Antimicrobial therapy was changed to Meropenem 500 mg 12 hourly and Teicoplanin 50 mg 24 hourly according to susceptibility report. She continued to have intermittent fever (99–101 F).
3.808594
0.982422
sec[1]/p[2]
en
0.999998
22779014
https://doi.org/10.1155/2012/257940
[ "gram", "mandible", "swab", "sent", "fungal", "teeth", "medullary", "site", "acid", "fast" ]
[ { "code": "1B74.Y", "title": "Superficial bacterial folliculitis due to other specified organism" }, { "code": "1C41&XN5PZ/1G40", "title": "Sepsis due to Gram-negative organisms without mention of septic shock" }, { "code": "1D01.0Z", "title": "Bacterial meningitis, unspecified" }, { "code": "KA22.0", "title": "Exceptionally large newborn" }, { "code": "MG50.Y", "title": "Other specified finding of gram negative bacteria resistant to antimicrobial drugs" }, { "code": "DA06.Z", "title": "Diseases of jaws, unspecified" }, { "code": "DA0E.0Y&XA51B7", "title": "Mandibular hypoplasia" }, { "code": "NA03.3", "title": "Strain or sprain of jaw" }, { "code": "DA0E.7", "title": "Dentofacial parafunctional disorders" }, { "code": "NA02.7Z", "title": "Fracture of mandible, unspecified" } ]
=== ICD-11 CODES FOUND === [1B74.Y] Superficial bacterial folliculitis due to other specified organism Also known as: Superficial bacterial folliculitis due to other specified organism | Superficial folliculitis associated with normal skin flora | Gram-negative folliculitis | Pseudomonas folliculitis | Hot tub folliculitis [1D01.0Z] Bacterial meningitis, unspecified Also known as: Bacterial meningitis, unspecified | Bacterial meningitis | BM - [bacterial meningitis] | leptomeningitis bacterial | pachymeningitis bacterial [KA22.0] Exceptionally large newborn Definition: An exceptionally large baby is defined as having a weight at birth of > 4500 g, regardless of gestational age at birth. Also known as: Exceptionally large newborn | Birth weight 4500 grams or more | macrosomia | excessively large fetus or infant | Oversize fetus Excludes: Syndrome of infant of mother with gestational diabetes | Syndrome of infant of a diabetic mother, type 1 or 2, nongestational, insulin dependent [MG50.Y] Other specified finding of gram negative bacteria resistant to antimicrobial drugs Also known as: Other specified finding of gram negative bacteria resistant to antimicrobial drugs | Carbapenem resistant gram negative bacteria, not elsewhere classified | Colistin resistant gram negative bacteria, not elsewhere classified [DA06.Z] Diseases of jaws, unspecified Also known as: Diseases of jaws, unspecified | Diseases of jaws | disease of jaw | diseases of the jaws | disorder of jaw [NA03.3] Strain or sprain of jaw Definition: A collective term for muscle and ligament injuries of the tissues associated with the mandible without dislocation or fracture; a joint injury in which some of the fibers of a supporting ligament are ruptured but the continuity of the ligament remains intact. A strain is an overstretching or overexertion of some part of the musculature. Also known as: Strain or sprain of jaw | strain of jaw | sprain of mandible | strain of mandible | sprain of temporomandibular joint [DA0E.7] Dentofacial parafunctional disorders Definition: Bruxism is a repetitive jaw-muscle activity characterised by clenching or grinding of the teeth and/or by bracing or thrusting of the mandible. Bruxism has two distinct circadian manifestations: it can occur during sleep (indicated as sleep bruxism) or during wakefulness (indicated as awake bruxism) Also known as: Dentofacial parafunctional disorders | Bruxism | Teeth-clenching | Teeth-grinding | Awake bruxism Excludes: Atypical facial pain | dyskinesia | trismus [NA02.7Z] Fracture of mandible, unspecified Also known as: Fracture of mandible, unspecified | Fracture of mandible | fracture of lower jaw | mandibular fracture | jaw fracture === GRAPH WALKS === --- Walk 1 --- [1B74.Y] Superficial bacterial folliculitis due to other specified organism --PARENT--> [1B74] Superficial bacterial folliculitis Def: Bacterial infection of the follicular ostium manifested as follicular papules and pustules with perifollicular erythema. The most commonly isolated organisms are coagulase-negative staphylococci and S... --CHILD--> [1B74.0] Staphylococcus aureus superficial folliculitis Def: Infection of the follicular ostium with Staphylococcus aureus. There is a predilection for hairy areas including the scalp, beard and thighs.... --- Walk 2 --- [1B74.Y] Superficial bacterial folliculitis due to other specified organism --PARENT--> [1B74] Superficial bacterial folliculitis Def: Bacterial infection of the follicular ostium manifested as follicular papules and pustules with perifollicular erythema. The most commonly isolated organisms are coagulase-negative staphylococci and S... --CHILD--> [1B74.Z] Superficial bacterial folliculitis due to unspecified organism --- Walk 3 --- [1D01.0Z] Bacterial meningitis, unspecified --PARENT--> [1D01.0] Bacterial meningitis Def: Any disease of the meninges, caused by an infection with a bacterial source.... --CHILD--> [1D01.00] Meningitis due to Haemophilus influenzae --- Walk 4 --- [1D01.0Z] Bacterial meningitis, unspecified --PARENT--> [1D01.0] Bacterial meningitis Def: Any disease of the meninges, caused by an infection with a bacterial source.... --EXCLUDES--> [?] Bacterial encephalitis --- Walk 5 --- [KA22.0] Exceptionally large newborn Def: An exceptionally large baby is defined as having a weight at birth of > 4500 g, regardless of gestational age at birth.... --EXCLUDES--> [?] Syndrome of infant of mother with gestational diabetes Def: Describes the range of effects on the infant born to a woman with gestational diabetes (onset or first recognition of carbohydrate intolerance of variable severity in pregnancy). Common neonatal effec... --PARENT--> [?] Transitory disorders of carbohydrate metabolism specific to fetus or newborn Def: A group of paediatric conditions in which there is a temporary disorder in a newborn or infant associated with abnormal chemical reactions in the body disrupting the process of getting or making energ... --- Walk 6 --- [KA22.0] Exceptionally large newborn Def: An exceptionally large baby is defined as having a weight at birth of > 4500 g, regardless of gestational age at birth.... --EXCLUDES--> [?] Syndrome of infant of a diabetic mother, type 1 or 2, nongestational, insulin dependent Def: Describes the range of effects on the infant born to a woman with pregestational diabetes mellitus (type 1 or type 2). Common neonatal effects include macrosomia, intrauterine growth restriction, birt... --CHILD--> [?] Diabetic embryopathy Def: Diabetic embryopathy is characterised by congenital anomalies or fetal/neonatal complications in an infant that are linked to diabetes in the mother: macrosomia, cardiovascular malformations such as l...
[ "[1B74.Y] Superficial bacterial folliculitis due to other specified organism\n --PARENT--> [1B74] Superficial bacterial folliculitis\n Def: Bacterial infection of the follicular ostium manifested as follicular papules and pustules with perifollicular erythema. The most commonly isolated organisms are coagulase-negative staphylococci and S...\n --CHILD--> [1B74.0] Staphylococcus aureus superficial folliculitis\n Def: Infection of the follicular ostium with Staphylococcus aureus. There is a predilection for hairy areas including the scalp, beard and thighs....", "[1B74.Y] Superficial bacterial folliculitis due to other specified organism\n --PARENT--> [1B74] Superficial bacterial folliculitis\n Def: Bacterial infection of the follicular ostium manifested as follicular papules and pustules with perifollicular erythema. The most commonly isolated organisms are coagulase-negative staphylococci and S...\n --CHILD--> [1B74.Z] Superficial bacterial folliculitis due to unspecified organism", "[1D01.0Z] Bacterial meningitis, unspecified\n --PARENT--> [1D01.0] Bacterial meningitis\n Def: Any disease of the meninges, caused by an infection with a bacterial source....\n --CHILD--> [1D01.00] Meningitis due to Haemophilus influenzae", "[1D01.0Z] Bacterial meningitis, unspecified\n --PARENT--> [1D01.0] Bacterial meningitis\n Def: Any disease of the meninges, caused by an infection with a bacterial source....\n --EXCLUDES--> [?] Bacterial encephalitis", "[KA22.0] Exceptionally large newborn\n Def: An exceptionally large baby is defined as having a weight at birth of > 4500 g, regardless of gestational age at birth....\n --EXCLUDES--> [?] Syndrome of infant of mother with gestational diabetes\n Def: Describes the range of effects on the infant born to a woman with gestational diabetes (onset or first recognition of carbohydrate intolerance of variable severity in pregnancy). Common neonatal effec...\n --PARENT--> [?] Transitory disorders of carbohydrate metabolism specific to fetus or newborn\n Def: A group of paediatric conditions in which there is a temporary disorder in a newborn or infant associated with abnormal chemical reactions in the body disrupting the process of getting or making energ...", "[KA22.0] Exceptionally large newborn\n Def: An exceptionally large baby is defined as having a weight at birth of > 4500 g, regardless of gestational age at birth....\n --EXCLUDES--> [?] Syndrome of infant of a diabetic mother, type 1 or 2, nongestational, insulin dependent\n Def: Describes the range of effects on the infant born to a woman with pregestational diabetes mellitus (type 1 or type 2). Common neonatal effects include macrosomia, intrauterine growth restriction, birt...\n --CHILD--> [?] Diabetic embryopathy\n Def: Diabetic embryopathy is characterised by congenital anomalies or fetal/neonatal complications in an infant that are linked to diabetes in the mother: macrosomia, cardiovascular malformations such as l..." ]
1B74.Y
Superficial bacterial folliculitis due to other specified organism
[ { "from_icd11": "1D01.0Z", "icd10_code": "G042", "icd10_title": "Bacterial meningoencephalitis and meningomyelitis, not elsewhere classified" }, { "from_icd11": "1D01.0Z", "icd10_code": "G009", "icd10_title": "Bacterial meningitis, unspecified" }, { "from_icd11": "1D01.0Z", "icd10_code": "G008", "icd10_title": "Other bacterial meningitis" }, { "from_icd11": "1D01.0Z", "icd10_code": "G01", "icd10_title": "Meningitis in bacterial diseases classified elsewhere" }, { "from_icd11": "1D01.0Z", "icd10_code": "G00", "icd10_title": "Bacterial meningitis, not elsewhere classified" }, { "from_icd11": "KA22.0", "icd10_code": "P080", "icd10_title": "Exceptionally large newborn baby" }, { "from_icd11": "NA03.3", "icd10_code": "S034", "icd10_title": "Sprain of jaw" }, { "from_icd11": "NA02.7Z", "icd10_code": "S02652A", "icd10_title": "Fracture of angle of left mandible, initial encounter for closed fracture" }, { "from_icd11": "NA02.7Z", "icd10_code": "S0262XA", "icd10_title": "" }, { "from_icd11": "NA02.7Z", "icd10_code": "S02610A", "icd10_title": "Fracture of condylar process of mandible, unspecified side, initial encounter for closed fracture" }, { "from_icd11": "NA02.7Z", "icd10_code": "S02641A", "icd10_title": "Fracture of ramus of right mandible, initial encounter for closed fracture" }, { "from_icd11": "NA02.7Z", "icd10_code": "S0269XA", "icd10_title": "Fracture of mandible of other specified site, initial encounter for closed fracture" }, { "from_icd11": "NA02.7Z", "icd10_code": "S0261XA", "icd10_title": "" }, { "from_icd11": "NA02.7Z", "icd10_code": "S0266XB", "icd10_title": "Fracture of symphysis of mandible, initial encounter for open fracture" }, { "from_icd11": "NA02.7Z", "icd10_code": "S0265XA", "icd10_title": "" } ]
G042
Bacterial meningoencephalitis and meningomyelitis, not elsewhere classified
Owing to the patient's poor general condition on admission, his caloric intake was increased gradually using intravenous nutrition before starting enteral nutrition. The intake could be titrated without causing electrolyte abnormalities that are known to occur as refeeding syndrome (such as hypophosphatemia or hypokalemia). After the resolution of intestinal edema, which was confirmed by sonography, enteral nutrition was initiated and increased gradually. Although he never threw up or had self-induced vomiting, he had a very slow oral intake and was unable to reach the target oral intake, so he was fed through a nasogastric tube. After being counseled that his life was in danger due to his extreme emaciation, his oral intake gradually increased and the nasogastric tube was discontinued by week 9. BMI decreased to 8.9 kg/m 2 after admission, but weight gain was steady after enteral feeding resumed. By the 12 th week of hospitalization, his BMI recovered to 13 kg/m 2 . By the 20 th week, it was 15; therefore, he was discharged . His BMI remained stable at approximately 16 kg/m 2 . Once the patient's condition was physically stabilized, psychiatric counseling and disease education were initiated. The patient has been followed up for about 2 years to date without any recurring eating disorders or weight loss. On follow-up, neither morphological changes on imaging nor the onset of epilepsy were noted.
3.720703
0.979004
sec[1]/p[3]
en
0.999998
38716398
https://doi.org/10.1155/2024/7478666
[ "intake", "gradually", "nutrition", "enteral", "oral", "without", "that", "initiated", "nasogastric", "tube" ]
[ { "code": "MG43.4Z", "title": "Insufficient intake of food or water due to self neglect, unspecified" }, { "code": "NE60", "title": "Harmful effects of drugs, medicaments or biological substances, not elsewhere classified" }, { "code": "MG43.41", "title": "Refusal of fluid, not elsewhere classified" }, { "code": "5B7Z", "title": "Unspecified undernutrition" }, { "code": "5B7Y", "title": "Other specified undernutrition" }, { "code": "5C3Z", "title": "Nutritional disorders, unspecified" }, { "code": "5C3Y", "title": "Other specified nutritional disorders" }, { "code": "QC45", "title": "Personal history of endocrine, nutritional or metabolic diseases" }, { "code": "1A40.Z", "title": "Infectious gastroenteritis or colitis without specification of infectious agent" }, { "code": "1A2Z", "title": "Viral intestinal infections, unspecified" } ]
=== ICD-11 CODES FOUND === [MG43.4Z] Insufficient intake of food or water due to self neglect, unspecified Also known as: Insufficient intake of food or water due to self neglect, unspecified | Insufficient intake of food or water due to self neglect | inadequate food intake | food intake poor | inadequate intake NOS [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 [MG43.41] Refusal of fluid, not elsewhere classified Also known as: Refusal of fluid, not elsewhere classified | stopped drinking | water intake inadequate Excludes: Intentional self-harm by lack of water | Dehydration [5B7Z] Unspecified undernutrition Also known as: Unspecified undernutrition | Malnutrition NOS | nutritional deficiency NOS | nutritional depletion NOS | severe malnutrition NOS [5B7Y] Other specified undernutrition Also known as: Other specified undernutrition | Undernutrition based on anthropometric or clinical criteria | Undernutrition based on anthropometric or clinical criteria in infants, children or adolescents | thinness NOS in infants, children or adolescents | Undernutrition based on anthropometric or clinical criteria in adults [5C3Z] Nutritional disorders, unspecified Also known as: Nutritional disorders, unspecified | nutritional disease NOS | disorder of nutrition | nutritional disturbance | Nutritional liver disease, not elsewhere classified [5C3Y] Other specified nutritional disorders Also known as: Other specified nutritional disorders | Dermatoses resulting from defective nutrition | Skin disorder attributable to malnutrition or malabsorption | Skin disorder attributable to food fads or unhealthy diet [QC45] Personal history of endocrine, nutritional or metabolic diseases Also known as: Personal history of endocrine, nutritional or metabolic diseases | history of endocrine disease or disorder | history of metabolic disease or disorder | history of nutritional disease or disorder | history of nutritional deficiency [1A40.Z] Infectious gastroenteritis or colitis without specification of infectious agent Also known as: Infectious gastroenteritis or colitis without specification of infectious agent | Gastroenteritis or colitis without specification of infectious agent | diarrhoea and gastroenteritis of presumed infectious origin | diarrhoeal enteritis | GE - [gastroenteritis] [1A2Z] Viral intestinal infections, unspecified Also known as: Viral intestinal infections, unspecified | viral and other specified intestinal infections | acute infectious viral gastroenteritis | infantile gastroenteritis virus | infantile viral gastroenteritis === GRAPH WALKS === --- Walk 1 --- [MG43.4Z] Insufficient intake of food or water due to self neglect, unspecified --PARENT--> [MG43.4] Insufficient intake of food or water due to self neglect --CHILD--> [MG43.4Y] Other specified insufficient intake of food or water due to self neglect --- Walk 2 --- [MG43.4Z] Insufficient intake of food or water due to self neglect, unspecified --PARENT--> [MG43.4] Insufficient intake of food or water due to self neglect --EXCLUDES--> [?] Intentional self-harm by lack of water --- 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... --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 4 --- [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 5 --- [MG43.41] Refusal of fluid, not elsewhere classified --EXCLUDES--> [?] Intentional self-harm by lack of water --PARENT--> [?] Intentional self-harm by exposure to other mechanism --- Walk 6 --- [MG43.41] Refusal of fluid, not elsewhere classified --EXCLUDES--> [?] Dehydration Def: 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... --PARENT--> [?] Volume depletion
[ "[MG43.4Z] Insufficient intake of food or water due to self neglect, unspecified\n --PARENT--> [MG43.4] Insufficient intake of food or water due to self neglect\n --CHILD--> [MG43.4Y] Other specified insufficient intake of food or water due to self neglect", "[MG43.4Z] Insufficient intake of food or water due to self neglect, unspecified\n --PARENT--> [MG43.4] Insufficient intake of food or water due to self neglect\n --EXCLUDES--> [?] Intentional self-harm by lack of water", "[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...", "[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...", "[MG43.41] Refusal of fluid, not elsewhere classified\n --EXCLUDES--> [?] Intentional self-harm by lack of water\n --PARENT--> [?] Intentional self-harm by exposure to other mechanism", "[MG43.41] Refusal of fluid, not elsewhere classified\n --EXCLUDES--> [?] Dehydration\n Def: 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...\n --PARENT--> [?] Volume depletion" ]
MG43.4Z
Insufficient intake of food or water due to self neglect, unspecified
[ { "from_icd11": "MG43.4Z", "icd10_code": "R636", "icd10_title": "Underweight" }, { "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": "" } ]
R636
Underweight
Included patients were operated in the chronological order displayed in Graph 2 . Patients 1 and 2 underwent LPA stenting and Venus P -valve implantation in different procedures, whereas for patient 3 this was done in the same procedure. The interventions took place in our cardiac catheter laboratory. All three patients underwent general anaesthesia and were operated via femoral access. 100 IU/kg heparin dose was administered with an additional heparin bolus when needed, maintaining ACT > 250 s throughout. Initially, a diagnostic angiographic catheter was used to take measurements of the RVOT, MPA and PA branches. At this point, the Venus P -valve of the appropriate size was selected. Then, an extra stiff guidewire (Lunderquist) was positioned distally into the RPA. A 26 Fr long/sheath (DrySeal GORE) was also advanced distally into to the RPA. The delivery system of the previously selected Venus P -valve was subsequently advanced into the long-sheath. The valve was deployed coming from the RPA but starting to open the distal valve flare into the MPA trunk, just below the LPA stent . This implantation technique avoided valve infolding, impingement, and dislocation. After valve deployment, stent patency was confirmed via pulmonary angiography. For patient 3, we placed, as planned, the LPA stent first and then we implanted the Venus P valve with the same modified technique used for patients 1 and 2.
3.978516
0.693359
sec[2]/sec[3]/p[0]
en
0.999997
38803661
https://doi.org/10.3389/fcvm.2024.1378924
[ "valve", "patients", "venus", "this", "stent", "operated", "implantation", "catheter", "heparin", "used" ]
[ { "code": "GB61.Z", "title": "Chronic kidney disease, stage unspecified" }, { "code": "BC00", "title": "Multiple valve disease" }, { "code": "BB9Z", "title": "Pulmonary valve disease, unspecified" }, { "code": "BB6Z", "title": "Mitral valve disease, unspecified" }, { "code": "LA8Z", "title": "Structural developmental anomaly of heart or great vessels, 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 === [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 [BC00] Multiple valve disease Also known as: Multiple valve disease | Multiple valve disease of unspecified origin | multiple valvular cardiac dysfunction | multivalvular cardiac dysfunction | Disorders of both mitral and aortic valves [BB9Z] Pulmonary valve disease, unspecified Also known as: Pulmonary valve disease, unspecified | rheumatic heart disease of pulmonary valve, unspecified | chronic rheumatic pulmonary valve endocarditis | chronic rheumatic pulmonary valvular endocarditis | rheumatic disease of pulmonary valve [BB6Z] Mitral valve disease, unspecified Also known as: Mitral valve disease, unspecified | noninfective endocarditis of mitral valve | rheumatic heart disease of mitral valve, unspecified | mitral valvulopathy | mitral valve cardiopathy [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 [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 --- [GB61.Z] Chronic kidney disease, stage unspecified --PARENT--> [GB61] Chronic kidney disease Def: Glomerular Filtration Rate (GFR) < 60 ml/min/1.73m² or presence of kidney damage that is present for more than 3 months. Evidence of kidney damage can include structural abnormalities (imaging or hist... --CHILD--> [GB61.2] Chronic kidney disease, stage 3a Def: GFR 45-59 ml/min/1.63m²... --- Walk 2 --- [GB61.Z] Chronic kidney disease, stage unspecified --PARENT--> [GB61] Chronic kidney disease Def: Glomerular Filtration Rate (GFR) < 60 ml/min/1.73m² or presence of kidney damage that is present for more than 3 months. Evidence of kidney damage can include structural abnormalities (imaging or hist... --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 ... --- Walk 3 --- [BC00] Multiple valve disease --PARENT--> [?] Heart valve diseases --CHILD--> [?] Aortic valve disease --- Walk 4 --- [BC00] Multiple valve disease --PARENT--> [?] Heart valve diseases --CHILD--> [?] Tricuspid valve disease --- Walk 5 --- [BB9Z] Pulmonary valve disease, unspecified --PARENT--> [?] Pulmonary valve disease --CHILD--> [BB91] Pulmonary valve insufficiency Def: Pulmonary valve insufficiency which is an incomplete closure of the pulmonary valve allows blood to return from pulmonary artery into the right ventricle.... --- Walk 6 --- [BB9Z] Pulmonary valve disease, unspecified --PARENT--> [?] Pulmonary valve disease --EXCLUDES--> [?] Congenital anomaly of pulmonary valve Def: A congenital malformation of the heart where the pulmonary valve is abnormal....
[ "[GB61.Z] Chronic kidney disease, stage unspecified\n --PARENT--> [GB61] Chronic kidney disease\n Def: Glomerular Filtration Rate (GFR) < 60 ml/min/1.73m² or presence of kidney damage that is present for more than 3 months. Evidence of kidney damage can include structural abnormalities (imaging or hist...\n --CHILD--> [GB61.2] Chronic kidney disease, stage 3a\n Def: GFR 45-59 ml/min/1.63m²...", "[GB61.Z] Chronic kidney disease, stage unspecified\n --PARENT--> [GB61] Chronic kidney disease\n Def: Glomerular Filtration Rate (GFR) < 60 ml/min/1.73m² or presence of kidney damage that is present for more than 3 months. Evidence of kidney damage can include structural abnormalities (imaging or hist...\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 ...", "[BC00] Multiple valve disease\n --PARENT--> [?] Heart valve diseases\n --CHILD--> [?] Aortic valve disease", "[BC00] Multiple valve disease\n --PARENT--> [?] Heart valve diseases\n --CHILD--> [?] Tricuspid valve disease", "[BB9Z] Pulmonary valve disease, unspecified\n --PARENT--> [?] Pulmonary valve disease\n --CHILD--> [BB91] Pulmonary valve insufficiency\n Def: Pulmonary valve insufficiency which is an incomplete closure of the pulmonary valve allows blood to return from pulmonary artery into the right ventricle....", "[BB9Z] Pulmonary valve disease, unspecified\n --PARENT--> [?] Pulmonary valve disease\n --EXCLUDES--> [?] Congenital anomaly of pulmonary valve\n Def: A congenital malformation of the heart where the pulmonary valve is abnormal...." ]
GB61.Z
Chronic kidney disease, stage unspecified
[ { "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": "BC00", "icd10_code": "I081", "icd10_title": "Rheumatic disorders of both mitral and tricuspid valves" }, { "from_icd11": "BC00", "icd10_code": "I080", "icd10_title": "Rheumatic disorders of both mitral and aortic valves" }, { "from_icd11": "BC00", "icd10_code": "I082", "icd10_title": "Rheumatic disorders of both aortic and tricuspid valves" }, { "from_icd11": "BC00", "icd10_code": "I083", "icd10_title": "Combined rheumatic disorders of mitral, aortic and tricuspid valves" }, { "from_icd11": "BC00", "icd10_code": "I088", "icd10_title": "Other rheumatic multiple valve diseases" }, { "from_icd11": "BC00", "icd10_code": "I089", "icd10_title": "Rheumatic multiple valve disease, unspecified" }, { "from_icd11": "BC00", "icd10_code": "I05-I09", "icd10_title": "" }, { "from_icd11": "BC00", "icd10_code": "I08", "icd10_title": "Multiple valve diseases" }, { "from_icd11": "BC00", "icd10_code": "I34", "icd10_title": "Nonrheumatic mitral valve disorders" }, { "from_icd11": "BC00", "icd10_code": "I35", "icd10_title": "Nonrheumatic aortic valve disorders" }, { "from_icd11": "BC00", "icd10_code": "I36", "icd10_title": "Nonrheumatic tricuspid valve disorders" } ]
N183
Chronic kidney disease, stage 3 (moderate)
In December 2022, a 43-year-old female patient with Scl-70 positive and rapidly-progressive SSc was admitted to our clinic for initiation of immunosuppressive treatment. Diagnosis of SSc with pulmonary and cardiac involvement had been established one year before. Initial modified Rodnan skin score (mRSS) was 32, forced vital capacity (FVC) was 79% predicted, and estimated glomerular filtration rate (eGFR, MDRD) was 99 ml/min (see Table 1 ). Assessment of mRSS was routinely performed by the same senior consultant in rheumatology during the case, an experienced investigator of the former ASTIS trial. Due to progressive skin manifestation, treatment with cyclophosphamide (cyc) 750mg/m² was initiated. After two cycles with initial treatment response, a flare with rapid skin progression occurred in January 2023 associated with stiffness, joint pain and severe impairment in daily activities. In this situation, the indication for aHSCT was set. Rituximab was administered in a dose of 1x 1000mg as a bridging therapy to transplant. Analogous to the ASTIS protocol, mobilization chemotherapy for stem cell apheresis containing cyc in a dose of 2000mg/m² per day on two consecutive days was used followed by stimulation with granulocyte colony-stimulating factor (G-CSF) in February 2023. After successful apheresis of CD34-selected stem cells, the patient was discharged with a slightly reduced eGFR of 72 ml/min.
4.015625
0.961914
sec[1]/p[0]
en
0.999997
PMC10693324
https://doi.org/10.3389/fimmu.2023.1294496
[ "skin", "mrss", "egfr", "astis", "stem", "apheresis", "december", "rapidly", "clinic", "initiation" ]
[ { "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" }, { "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 === [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 [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 --- [ME67] Skin disorder of uncertain or unspecified nature Def: 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.... --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--> [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... --- Walk 2 --- [ME67] Skin disorder of uncertain or unspecified nature Def: 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.... --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--> [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... --- Walk 3 --- [ME66.Y] Other specified skin changes --PARENT--> [ME66] Miscellaneous non-specific skin-related symptoms and signs Def: Other specified skin changes which cannot be more precisely defined.... --CHILD--> [ME66.2] Excess and redundant skin Def: A condition which typically occurs in formerly grossly obese individuals following massive weight loss, as following bariatric surgery or severe calorie restriction.... --- Walk 4 --- [ME66.Y] Other specified skin changes --PARENT--> [ME66] Miscellaneous non-specific skin-related symptoms and signs Def: Other specified skin changes which cannot be more precisely defined.... --RELATED_TO--> [?] Abnormal skin pigmentation Def: Abnormal skin pigmentation without specification of type or cause.... --- Walk 5 --- [EM0Y] Other specified diseases of the skin --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... --CHILD--> [?] Inflammatory dermatoses Def: A large group of skin disorders in which inflammation plays an important role.... --- Walk 6 --- [EM0Y] Other specified diseases of the skin --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... --RELATED_TO--> [?] Haematoma of surgical wound of skin Def: Collection of blood within skin and soft tissues following surgical wound of skin usually resulting from defective haemostasis...
[ "[ME67] Skin disorder of uncertain or unspecified nature\n Def: 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....\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--> [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...", "[ME67] Skin disorder of uncertain or unspecified nature\n Def: 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....\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--> [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...", "[ME66.Y] Other specified skin changes\n --PARENT--> [ME66] Miscellaneous non-specific skin-related symptoms and signs\n Def: Other specified skin changes which cannot be more precisely defined....\n --CHILD--> [ME66.2] Excess and redundant skin\n Def: A condition which typically occurs in formerly grossly obese individuals following massive weight loss, as following bariatric surgery or severe calorie restriction....", "[ME66.Y] Other specified skin changes\n --PARENT--> [ME66] Miscellaneous non-specific skin-related symptoms and signs\n Def: Other specified skin changes which cannot be more precisely defined....\n --RELATED_TO--> [?] Abnormal skin pigmentation\n Def: Abnormal skin pigmentation without specification of type or cause....", "[EM0Y] Other specified diseases of the skin\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...\n --CHILD--> [?] Inflammatory dermatoses\n Def: A large group of skin disorders in which inflammation plays an important role....", "[EM0Y] Other specified diseases of the skin\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...\n --RELATED_TO--> [?] Haematoma of surgical wound of skin\n Def: Collection of blood within skin and soft tissues following surgical wound of skin usually resulting from defective haemostasis..." ]
ME67
Skin disorder of uncertain or unspecified nature
[ { "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" }, { "from_icd11": "GB61.1", "icd10_code": "N182", "icd10_title": "Chronic kidney disease, stage 2 (mild)" }, { "from_icd11": "GB61.5", "icd10_code": "N186", "icd10_title": "End stage renal disease" }, { "from_icd11": "GB61.5", "icd10_code": "N185", "icd10_title": "Chronic kidney disease, stage 5" }, { "from_icd11": "GB61.4", "icd10_code": "N184", "icd10_title": "Chronic kidney disease, stage 4 (severe)" }, { "from_icd11": "GB61.3", "icd10_code": "N183", "icd10_title": "Chronic kidney disease, stage 3 (moderate)" }, { "from_icd11": "GB61.0", "icd10_code": "N181", "icd10_title": "Chronic kidney disease, stage 1" } ]
L989
Disorder of the skin and subcutaneous tissue, unspecified
A 63-year-old woman, with a history of Boerhaave's oesophageal rupture status post-oesophagectomy with extra-thoracic transverse colon interposition 40 years ago, presented with two weeks of malaise and was found to have a non-mechanical primary bowel dysmotility. She was dehydrated and resuscitated in the emergency room with intravenous (IV) normal saline which was later switched to IV 5% dextrose normal saline. Over the next week, she became progressively more lethargic and was thought to be delirious with “sundowning”. On neurologic examination, she was drowsy but arousable to verbal stimuli with bilateral vertical and horizontal ophthalmoplegia. An MRI of the brain showed symmetrical hyperintensity in the bilateral medial thalami and dorsal midbrain, including periaqueductal grey matter, as shown in Figure 1 . She was started on high-dose IV thiamine (500 mg three times daily for two days followed by 250 mg daily for five days followed by oral treatment with 100 mg daily) along with other B-complex vitamins and magnesium. Repeat brain MRI one week later showed significantly reduced hyperintensities in the thalamus and the dorsal midbrain region. Unfortunately, her hospital course was complicated by Pseudomonas and Klebsiella pneumonia requiring intubation, along with sepsis and progressive multiple organ failure. She passed away after the goal of her care was changed to comfort measures only.
3.876953
0.982422
sec[1]/p[0]
en
0.999998
30364782
https://doi.org/10.7759/cureus.3187
[ "daily", "saline", "brain", "midbrain", "along", "boerhaave", "oesophageal", "rupture", "status", "oesophagectomy" ]
[ { "code": "QF21", "title": "Difficulty or need for assistance with general life tasks or life management" }, { "code": "8A83", "title": "Other primary headache disorder" }, { "code": "QB42", "title": "Dependence on renal dialysis" }, { "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" }, { "code": "PH48", "title": "Exposure to or harmful effects of undetermined intent of other or unspecified drugs, medicaments or biological substances" }, { "code": "PE88", "title": "Assault by exposure to or harmful effects of other or unspecified drug, medicament or biological substance" }, { "code": "8E7Y", "title": "Other specified diseases of the nervous system" }, { "code": "LA05.Z", "title": "Cerebral structural developmental anomalies, unspecified" } ]
=== ICD-11 CODES FOUND === [QF21] Difficulty or need for assistance with general life tasks or life management Also known as: Difficulty or need for assistance with general life tasks or life management | difficulty with carrying out tasks and daily routine | life management problem | difficulty with life management tasks | Difficulty with dealing with change such as relocation Includes: difficulty with carrying out tasks and daily routine [8A83] Other primary headache disorder Definition: A group of clinically heterogeneous headache disorders, believed to be primary. Although largely unrelated, they fall into four categories: headaches associated with physical exertion; headaches attributed to direct physical but innocuous stimuli; epicranial headaches; and other miscellaneous primary headache disorders. Also known as: Other primary headache disorder | Primary cough headache | Primary exercise headache | Primary headache associated with sexual activity | Preorgasmic headache [QB42] Dependence on renal dialysis Also known as: Dependence on renal dialysis | renal dialysis status | presence of arteriovenous shunt for dialysis | dependence on haemodialysis | Dependence on renal dialysis, acute haemodialysis Includes: renal dialysis status Excludes: dialysis preparation, treatment or session [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 [PH48] Exposure to or harmful effects of undetermined intent of other or unspecified drugs, medicaments or biological substances Also known as: Exposure to or harmful effects of undetermined intent of other or unspecified drugs, medicaments or biological substances | drug related harm | Exposure to or harmful effects of undetermined intent of systemic antibiotics | Exposure to or harmful effects of undetermined intent of penicillins | Exposure to or harmful effects of undetermined intent of cephalosporins or other beta-lactam antibiotics [PE88] Assault by exposure to or harmful effects of other or unspecified drug, medicament or biological substance Also known as: Assault by exposure to or harmful effects of other or unspecified drug, medicament or biological substance | homicidal poisoning by exposure to or harmful effects of other or unspecified drug, medicament or biological substance | Assault by exposure to or harmful effects of systemic antibiotics | Assault by exposure to or harmful effects of penicillins | Assault by exposure to or harmful effects of cephalosporins or other beta-lactam antibiotics [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 [LA05.Z] Cerebral structural developmental anomalies, unspecified Also known as: Cerebral structural developmental anomalies, unspecified | Cerebral structural developmental anomalies | Malformations of brain | brain abnormality NOS | brain deformity NOS === GRAPH WALKS === --- Walk 1 --- [QF21] Difficulty or need for assistance with general life tasks or life management --PARENT--> [?] Difficulty or need for assistance with activities Def: Identifies activities for which the person needs assistance or has such difficulty with, that it affects their need for health services or their treatment.... --EXCLUDES--> [?] Dependence on enabling machines or devices --- Walk 2 --- [QF21] Difficulty or need for assistance with general life tasks or life management --PARENT--> [?] Difficulty or need for assistance with activities Def: Identifies activities for which the person needs assistance or has such difficulty with, that it affects their need for health services or their treatment.... --EXCLUDES--> [?] Dependence on enabling machines or devices --- Walk 3 --- [8A83] Other primary headache disorder Def: A group of clinically heterogeneous headache disorders, believed to be primary. Although largely unrelated, they fall into four categories: headaches associated with physical exertion; headaches attri... --PARENT--> [?] Headache disorders --CHILD--> [8A81] Tension-type headache Def: A primary and highly prevalent headache disorder, in most cases episodic. Attacks of highly variable frequency and duration are characterised by mild-to-moderate headache without associated symptoms, ... --- Walk 4 --- [8A83] Other primary headache disorder Def: A group of clinically heterogeneous headache disorders, believed to be primary. Although largely unrelated, they fall into four categories: headaches associated with physical exertion; headaches attri... --PARENT--> [?] Headache disorders --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 5 --- [QB42] Dependence on renal dialysis --PARENT--> [?] Dependence on enabling machines or devices --CHILD--> [QB40] Dependence on aspirator --- Walk 6 --- [QB42] Dependence on renal dialysis --PARENT--> [?] Dependence on enabling machines or devices --CHILD--> [QB42] Dependence on renal dialysis
[ "[QF21] Difficulty or need for assistance with general life tasks or life management\n --PARENT--> [?] Difficulty or need for assistance with activities\n Def: Identifies activities for which the person needs assistance or has such difficulty with, that it affects their need for health services or their treatment....\n --EXCLUDES--> [?] Dependence on enabling machines or devices", "[QF21] Difficulty or need for assistance with general life tasks or life management\n --PARENT--> [?] Difficulty or need for assistance with activities\n Def: Identifies activities for which the person needs assistance or has such difficulty with, that it affects their need for health services or their treatment....\n --EXCLUDES--> [?] Dependence on enabling machines or devices", "[8A83] Other primary headache disorder\n Def: A group of clinically heterogeneous headache disorders, believed to be primary. Although largely unrelated, they fall into four categories: headaches associated with physical exertion; headaches attri...\n --PARENT--> [?] Headache disorders\n --CHILD--> [8A81] Tension-type headache\n Def: A primary and highly prevalent headache disorder, in most cases episodic. Attacks of highly variable frequency and duration are characterised by mild-to-moderate headache without associated symptoms, ...", "[8A83] Other primary headache disorder\n Def: A group of clinically heterogeneous headache disorders, believed to be primary. Although largely unrelated, they fall into four categories: headaches associated with physical exertion; headaches attri...\n --PARENT--> [?] Headache disorders\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....", "[QB42] Dependence on renal dialysis\n --PARENT--> [?] Dependence on enabling machines or devices\n --CHILD--> [QB40] Dependence on aspirator", "[QB42] Dependence on renal dialysis\n --PARENT--> [?] Dependence on enabling machines or devices\n --CHILD--> [QB42] Dependence on renal dialysis" ]
QF21
Difficulty or need for assistance with general life tasks or life management
[ { "from_icd11": "QF21", "icd10_code": "Z742", "icd10_title": "Need for assistance at home and no other household member able to render care" }, { "from_icd11": "QF21", "icd10_code": "Z600", "icd10_title": "Problems of adjustment to life-cycle transitions" }, { "from_icd11": "8A83", "icd10_code": "G44209", "icd10_title": "Tension-type headache, unspecified, not intractable" }, { "from_icd11": "8A83", "icd10_code": "G44221", "icd10_title": "Chronic tension-type headache, intractable" }, { "from_icd11": "8A83", "icd10_code": "G44229", "icd10_title": "Chronic tension-type headache, not intractable" }, { "from_icd11": "8A83", "icd10_code": "G44201", "icd10_title": "Tension-type headache, unspecified, intractable" }, { "from_icd11": "8A83", "icd10_code": "G44219", "icd10_title": "Episodic tension-type headache, not intractable" }, { "from_icd11": "8A83", "icd10_code": "G442", "icd10_title": "Tension-type headache" }, { "from_icd11": "QB42", "icd10_code": "Z992", "icd10_title": "Dependence on renal dialysis" }, { "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" } ]
Z742
Need for assistance at home and no other household member able to render care
A 51-year-old male presented to the emergency department complaining of fever lasting for 20 days, shortness of breath, chest tightness, and a cough spanning 4 days. He had no significant past medical history. His body temperature was 37.5°C, his blood pressure was 102/76 mm Hg, his heart rate was 109 beats per minute, and his physical examination was generally normal. Laboratory studies showed a white blood cell (WBC) count of 14.9 × 10 9 /L (reference range, 3.5–9.5 × 10 9 /L). Results also indicated troponin T to be 5.26 ng/mL (reference range, 0–0.11 ng/mL); creatine kinase (CK) 300 IU/L (reference range, 24–194 IU/L); creatine kinase enzymes (CKMB) 33 IU/L (reference range, 0–24 IU/L); and C-reactive protein (CRP) 9.1 mg/L (reference range, 0.0–5.0 mg/L). Chest computed tomography (CT) showed a moderate amount of pleural effusion with bilateral partial atelectasis and pericardial effusion . ECG on admission revealed sinus tachycardia, critical low voltage of limb lead, mild depression of the ST segment of the anterior wall lead, and a prolonged critical QT interval. Transthoracic echocardiography showed diffuse concentric LV hypertrophy with depressed LV diastolic function and a small pericardial effusion, which had been misdiagnosed as restrictive cardiomyopathy. The patient subsequently underwent coronary angiography, which demonstrated normal coronary anatomy with a right dominant system.
3.974609
0.97998
sec[1]/p[0]
en
0.999998
32080118
https://doi.org/10.1097/MD.0000000000019223
[ "reference", "range", "effusion", "chest", "blood", "creatine", "kinase", "pericardial", "critical", "lead" ]
[ { "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": "FA36.Z", "title": "Effusion of joint, unspecified" }, { "code": "1D01.Z", "title": "Infectious meningitis, 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 [FA36.Z] Effusion of joint, unspecified Also known as: Effusion of joint, unspecified | Effusion of joint | effusion into joint | effusion of joint, site unspecified | hydrarthrosis [1D01.Z] Infectious meningitis, unspecified Also known as: Infectious meningitis, unspecified | Infectious meningitis, not elsewhere classified | acute meningomyelitis | septic meningitis NOS | infectious meningitis NEC === 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... --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 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--> [MB26.02] Delusion of guilt Def: A delusion involving exaggerated or inappropriate responsibility, need for punishment or retribution, or disproportionate consequences of one’s actions, such as that a minor error in the past will lea... --- 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.Z] Olfactory reference disorder, unspecified --- 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... --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...
[ "[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 --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....", "[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--> [MB26.02] Delusion of guilt\n Def: A delusion involving exaggerated or inappropriate responsibility, need for punishment or retribution, or disproportionate consequences of one’s actions, such as that a minor error in the past will lea...", "[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", "[6B22.1] 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 --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..." ]
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": "FA36.Z", "icd10_code": "M25471", "icd10_title": "Effusion, right ankle" }, { "from_icd11": "FA36.Z", "icd10_code": "M25461", "icd10_title": "Effusion, right knee" }, { "from_icd11": "FA36.Z", "icd10_code": "M25462", "icd10_title": "Effusion, left knee" }, { "from_icd11": "FA36.Z", "icd10_code": "M25431", "icd10_title": "Effusion, right wrist" }, { "from_icd11": "FA36.Z", "icd10_code": "M25472", "icd10_title": "Effusion, left ankle" }, { "from_icd11": "FA36.Z", "icd10_code": "M25451", "icd10_title": "Effusion, right hip" }, { "from_icd11": "FA36.Z", "icd10_code": "M2548", "icd10_title": "Effusion, other site" }, { "from_icd11": "FA36.Z", "icd10_code": "M25411", "icd10_title": "Effusion, right shoulder" }, { "from_icd11": "FA36.Z", "icd10_code": "M25441", "icd10_title": "Effusion, right hand" }, { "from_icd11": "FA36.Z", "icd10_code": "M25452", "icd10_title": "Effusion, left hip" }, { "from_icd11": "FA36.Z", "icd10_code": "M25421", "icd10_title": "Effusion, right elbow" }, { "from_icd11": "FA36.Z", "icd10_code": "M25432", "icd10_title": "Effusion, left wrist" } ]
F428
Other obsessive-compulsive disorder
An 81-year-old woman was referred to the emergency department from the nephrology office for low blood pressure. She had nausea and occasional episodes of vomiting, and also reported metallic/salty taste in her mouth and a low appetite which she attributed to the use of spironolactone she had been taking for a month. She had an aortic valve replacement surgery four months back after which she went into respiratory, hepatic and renal failure, and disseminated intravascular coagulation (DIC). The hepatic failure resolved, but she had not been feeling well and had been since living at home with her son who helped her with most of her activities. For the past six months, she had been having alternating constipation and diarrhea and also lost about 40 pounds during this time; however, she denied any fever, dysphagia, odynophagia, abdominal pain, melena, and hematochezia. She also had a temporary episode of facial drooping and swaying to the left side four to five days back, where she did not go to the emergency department but was started on aspirin by her primary care physician. She had a history of chronic obstructive pulmonary disease (COPD), hypertension, high cholesterol, hypothyroidism, paroxysmal atrial fibrillation, hysterectomy, tonsillectomy, adenoidectomy, and cataract surgery. She quit smoking two months back after smoking one pack daily for the past 60 years, and had a glass of wine daily.
3.5
0.988281
sec[1]/p[0]
en
0.999996
31598442
https://doi.org/10.7759/cureus.5335
[ "back", "emergency", "department", "which", "four", "hepatic", "failure", "past", "smoking", "daily" ]
[ { "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": "JB22.1", "title": "Delivery by emergency caesarean section" }, { "code": "RA09", "title": "International emergency code 10" }, { "code": "BA03", "title": "Hypertensive crisis" }, { "code": "RA00", "title": "Conditions of uncertain aetiology and emergency use" }, { "code": "RA04", "title": "International emergency code 05" } ]
=== 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 [JB22.1] Delivery by emergency caesarean section Also known as: Delivery by emergency caesarean section | emergency caesarean [RA09] International emergency code 10 Also known as: International emergency code 10 [BA03] Hypertensive crisis Also known as: Hypertensive crisis | Hypertensive emergency | hypertensive crisis with acute organ damage | severely elevated blood pressure with acute organ damage | Hypertensive urgency [RA00] Conditions of uncertain aetiology and emergency use Also known as: Conditions of uncertain aetiology and emergency use [RA04] International emergency code 05 Also known as: International emergency code 05 === GRAPH WALKS === --- Walk 1 --- [ND51.0] Dislocation or strain or sprain of unspecified joint or ligament of trunk --PARENT--> [ND51] Other injuries of spine or trunk, level unspecified --EXCLUDES--> [?] Crushing injuries involving multiple body regions --- Walk 2 --- [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 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.... --PARENT--> [?] Symptoms or signs of the musculoskeletal system --- 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.... --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... --- Walk 5 --- [ND51.Y] Other specified injuries of spine or trunk, level unspecified --PARENT--> [ND51] Other injuries of spine or trunk, level unspecified --EXCLUDES--> [?] Injuries of intrathoracic organs with intra-abdominal or pelvic organs --- Walk 6 --- [ND51.Y] Other specified injuries of spine or trunk, level unspecified --PARENT--> [ND51] Other injuries of spine or trunk, level unspecified --CHILD--> [ND51.2] Injury of spinal cord, level unspecified
[ "[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 --EXCLUDES--> [?] Crushing injuries involving multiple body regions", "[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....", "[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 --PARENT--> [?] Symptoms or signs of the musculoskeletal system", "[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 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...", "[ND51.Y] Other specified injuries of spine or trunk, level unspecified\n --PARENT--> [ND51] Other injuries of spine or trunk, level unspecified\n --EXCLUDES--> [?] Injuries of intrathoracic organs with intra-abdominal or pelvic organs", "[ND51.Y] Other specified injuries of spine or trunk, level unspecified\n --PARENT--> [ND51] Other injuries of spine or trunk, level unspecified\n --CHILD--> [ND51.2] Injury of spinal cord, level unspecified" ]
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
Ring chromosome 20 syndrome is a rare chromosomal disorder associated with refractory epilepsy, as well as cognitive and behavioral impairments as impulsivity or aggressiveness. Child psychiatrists and neurologists are challenged by these severe symptoms. Antipsychotics may impact the seizure threshold, with a risk of increasing the number of seizures. Hence, it is complicated to initiate psychiatric medication when behavioral disorders are an expression of resistant epileptic disease. Here, we report the case of a 12‐year‐old girl, diagnosed with ring chromosome 20 syndrome. Clinical features included refractory focal impaired awareness seizures, in spite of antiepileptic polymedication, and major cognitive and behavioral impairments. Cognitive impairments were attention, memory, and executive deficit, and behavioral impairments were aggressiveness, irritability, disinhibition, and hyperactivity. As mood symptoms were fluctuant and could be considered as bipolar disorder not otherwise specified (BP‐NOS), we decided to introduce lithium. This treatment was very efficient with an improvement not only in behavioral symptoms but also in epilepsy. Then, we discuss the link between lithium treatment and possible pathophysiology in ring chromosome 20 syndrome. We suggest a possible effect of lithium on KCNQ2 gene that has been associated with some forms of epileptic disease as well as bipolar disorder.
4.191406
0.943359
sec[0]/p[0]
en
0.999996
30455928
https://doi.org/10.1002/ccr3.1796
[ "behavioral", "impairments", "ring", "chromosome", "cognitive", "lithium", "associated", "refractory", "epilepsy", "well" ]
[ { "code": "MB23.Z", "title": "Symptoms and signs involving appearance and behaviour, unspecified" }, { "code": "MB23.8", "title": "Disruptive behaviour" }, { "code": "MB23.N", "title": "Psychomotor retardation" }, { "code": "MB23.0", "title": "Aggressive behaviour" }, { "code": "MB23.2", "title": "Avoidance behaviour" }, { "code": "9D9Z", "title": "Vision impairment, unspecified" }, { "code": "GB6Z", "title": "Kidney failure, unspecified" }, { "code": "MB21.Z", "title": "Symptoms, signs or clinical findings involving cognition, unspecified" }, { "code": "AB52", "title": "Deafness not otherwise specified" }, { "code": "DB97.Y", "title": "Other specified inflammatory liver disease" } ]
=== ICD-11 CODES FOUND === [MB23.Z] Symptoms and signs involving appearance and behaviour, unspecified Also known as: Symptoms and signs involving appearance and behaviour, unspecified | Symptoms or signs involving appearance or behaviour | self neglect NOS | abnormal behaviour NOS [MB23.8] Disruptive behaviour Definition: Behaviour that causes disorder and turmoil in others or one's environment (e.g., angry outbursts, arguments, disobedience). Also known as: Disruptive behaviour Excludes: Disruptive behaviour or dissocial disorders [MB23.N] Psychomotor retardation Definition: A visible generalised slowing of movements and speech. Also known as: Psychomotor retardation | slowness and poor responsiveness | slow behaviour | poor responsiveness behaviour Excludes: Stupor [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 [MB23.2] Avoidance behaviour Definition: The act of keeping away from circumstances, situations, or stimuli that cause anxiety or other negative emotions in the individual. Also known as: Avoidance behaviour [9D9Z] Vision impairment, unspecified Also known as: Vision impairment, unspecified | sight impaired | blindness and low vision | impaired vision [GB6Z] Kidney failure, unspecified Also known as: Kidney failure, unspecified | nontraumatic kidney injury | renal failure NOS | kidney block | renal impairment NOS [MB21.Z] Symptoms, signs or clinical findings involving cognition, unspecified Also known as: Symptoms, signs or clinical findings involving cognition, unspecified | Symptoms, signs or clinical findings involving cognition | cognitive impairment NOS [AB52] Deafness not otherwise specified Also known as: Deafness not otherwise specified | deaf | hearing loss NOS | hearing impairment | hearing loss [DB97.Y] Other specified inflammatory liver disease Also known as: Other specified inflammatory liver disease | Hepatocholangitis | Cholestatic hepatitis | Cholangiolitic hepatitis | Acute active liver inflammation === GRAPH WALKS === --- Walk 1 --- [MB23.Z] Symptoms and signs involving appearance and behaviour, unspecified --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.... --- Walk 2 --- [MB23.Z] Symptoms and signs involving appearance and behaviour, unspecified --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 3 --- [MB23.8] Disruptive behaviour Def: Behaviour that causes disorder and turmoil in others or one's environment (e.g., angry outbursts, arguments, disobedience).... --EXCLUDES--> [?] Disruptive behaviour or dissocial disorders Def: Disruptive behaviour and dissocial disorders are characterised by persistent behaviour problems that range from markedly and persistently defiant, disobedient, provocative or spiteful (i.e., disruptiv... --CHILD--> [?] Conduct-dissocial disorder Def: Conduct-dissocial disorder is characterised by a repetitive and persistent pattern of behaviour in which the basic rights of others or major age-appropriate societal norms, rules, or laws are violated... --- Walk 4 --- [MB23.8] Disruptive behaviour Def: Behaviour that causes disorder and turmoil in others or one's environment (e.g., angry outbursts, arguments, disobedience).... --EXCLUDES--> [?] Disruptive behaviour or dissocial disorders Def: Disruptive behaviour and dissocial disorders are characterised by persistent behaviour problems that range from markedly and persistently defiant, disobedient, provocative or spiteful (i.e., disruptiv... --CHILD--> [?] Conduct-dissocial disorder Def: Conduct-dissocial disorder is characterised by a repetitive and persistent pattern of behaviour in which the basic rights of others or major age-appropriate societal norms, rules, or laws are violated... --- Walk 5 --- [MB23.N] Psychomotor retardation Def: A visible generalised slowing of movements and speech.... --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.N] Psychomotor retardation Def: A visible generalised slowing of movements and speech.... --EXCLUDES--> [?] Stupor Def: Total or nearly total lack of spontaneous movement and marked decrease in reactivity to environment.... --EXCLUDES--> [?] Catatonia Def: Catatonia is a syndrome of primarily psychomotor disturbances, characterized by the co-occurrence of several symptoms of decreased, increased, or abnormal psychomotor activity. The assessment of catat...
[ "[MB23.Z] Symptoms and signs involving appearance and behaviour, unspecified\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....", "[MB23.Z] Symptoms and signs involving appearance and behaviour, unspecified\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...", "[MB23.8] Disruptive behaviour\n Def: Behaviour that causes disorder and turmoil in others or one's environment (e.g., angry outbursts, arguments, disobedience)....\n --EXCLUDES--> [?] Disruptive behaviour or dissocial disorders\n Def: Disruptive behaviour and dissocial disorders are characterised by persistent behaviour problems that range from markedly and persistently defiant, disobedient, provocative or spiteful (i.e., disruptiv...\n --CHILD--> [?] Conduct-dissocial disorder\n Def: Conduct-dissocial disorder is characterised by a repetitive and persistent pattern of behaviour in which the basic rights of others or major age-appropriate societal norms, rules, or laws are violated...", "[MB23.8] Disruptive behaviour\n Def: Behaviour that causes disorder and turmoil in others or one's environment (e.g., angry outbursts, arguments, disobedience)....\n --EXCLUDES--> [?] Disruptive behaviour or dissocial disorders\n Def: Disruptive behaviour and dissocial disorders are characterised by persistent behaviour problems that range from markedly and persistently defiant, disobedient, provocative or spiteful (i.e., disruptiv...\n --CHILD--> [?] Conduct-dissocial disorder\n Def: Conduct-dissocial disorder is characterised by a repetitive and persistent pattern of behaviour in which the basic rights of others or major age-appropriate societal norms, rules, or laws are violated...", "[MB23.N] Psychomotor retardation\n Def: A visible generalised slowing of movements and speech....\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.N] Psychomotor retardation\n Def: A visible generalised slowing of movements and speech....\n --EXCLUDES--> [?] Stupor\n Def: Total or nearly total lack of spontaneous movement and marked decrease in reactivity to environment....\n --EXCLUDES--> [?] Catatonia\n Def: Catatonia is a syndrome of primarily psychomotor disturbances, characterized by the co-occurrence of several symptoms of decreased, increased, or abnormal psychomotor activity. The assessment of catat..." ]
MB23.Z
Symptoms and signs involving appearance and behaviour, unspecified
[ { "from_icd11": "MB23.Z", "icd10_code": "R4689", "icd10_title": "Other symptoms and signs involving appearance and behavior" }, { "from_icd11": "MB23.Z", "icd10_code": "R4681", "icd10_title": "Obsessive-compulsive behavior" }, { "from_icd11": "MB23.Z", "icd10_code": "R46", "icd10_title": "Symptoms and signs involving appearance and behavior" }, { "from_icd11": "MB23.Z", "icd10_code": "R466", "icd10_title": "Undue concern and preoccupation with stressful events" }, { "from_icd11": "MB23.Z", "icd10_code": "R468", "icd10_title": "Other symptoms and signs involving appearance and behavior" }, { "from_icd11": "MB23.N", "icd10_code": "R464", "icd10_title": "Slowness and poor responsiveness" }, { "from_icd11": "MB23.0", "icd10_code": "R456", "icd10_title": "Violent behavior" }, { "from_icd11": "9D9Z", "icd10_code": "H547", "icd10_title": "Unspecified visual loss" }, { "from_icd11": "9D9Z", "icd10_code": "H53-H54", "icd10_title": "" }, { "from_icd11": "9D9Z", "icd10_code": "H54", "icd10_title": "Blindness and low vision" }, { "from_icd11": "9D9Z", "icd10_code": "H549", "icd10_title": "" }, { "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": "MB21.Z", "icd10_code": "R419", "icd10_title": "Unspecified symptoms and signs involving cognitive functions and awareness" } ]
R4689
Other symptoms and signs involving appearance and behavior
As we sum up the case, cerebellar ataxia was the dominant feature at onset, which was rapidly followed by focal dystonia. Cognitive decline appeared somewhat late in the temporal course of events accompanied by typical myoclonic jerks. Our patient was in a terminal akinetic mute state within a span of a mere 30 days. Keeping in mind the clinical scenario, short duration (1 month) of illness, and rapid downhill course, our top differentials were primary and secondary brain neoplasms, metabolic derangement, infective encephalopathy, autoimmune (including paraneoplastic) encephalitis, and prion disease. However, all the available metabolic parameters were within normal limits. Infective or autoimmune encephalitis was also discounted after CSF analysis and culture turned out to be negative. Paraneoplastic markers in CSF also were non-contributory. As diffusion-weighted sequence of MRI of our patient’s brain revealed bilateral caudate hyperintensity as well as ribbon pattern in cortex, suggestive of sporadic CJD, we concentrated on prion disease. Serial EEG recordings in our patient revealed gradual slowing of the background activity with more obvious appearance of bi-hemispheric triphasic waves and nearly typical periodic sharp wave complexes. After 14-3-3 protein was detected positive in CSF sample, a diagnosis of probable sporadic CJD was made according to the current European diagnostic criteria .
4.121094
0.96875
sec[2]/p[0]
en
0.999997
31138302
https://doi.org/10.1186/s13256-019-2089-5
[ "course", "typical", "within", "brain", "metabolic", "infective", "autoimmune", "paraneoplastic", "encephalitis", "prion" ]
[ { "code": "LA8Y", "title": "Other specified structural developmental anomaly of heart or great vessels" }, { "code": "8B10.Y", "title": "Other specified transient ischaemic attack" }, { "code": "6A80", "title": "Symptomatic and course presentations for mood episodes in mood disorders" }, { "code": "LA8C.1", "title": "Anomalous aortic origin or course of coronary artery" }, { "code": "8B22.Y", "title": "Other specified cerebrovascular disease" }, { "code": "5C50.00", "title": "Classical phenylketonuria" }, { "code": "1D40", "title": "Chikungunya virus disease" }, { "code": "8A68.2", "title": "Absence seizures, typical" }, { "code": "8C72.00", "title": "Nemaline myopathy" }, { "code": "DA90.0", "title": "Syndromic diarrhoea" } ]
=== 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 [8B10.Y] Other specified transient ischaemic attack Also known as: Other specified transient ischaemic attack | Vertebrobasilar artery syndrome | vertebrobasilar arterial insufficiency | vertebrobasilar insufficiency | vertebro-basilar artery syndrome, course of resolution unspecified [6A80] Symptomatic and course presentations for mood episodes in mood disorders Definition: These categories may be applied to describe the presentation and characteristics of mood episodes in the context of single episode depressive disorder, recurrent depressive disorder, bipolar type I disorder, or bipolar type II disorder. These categories indicate the presence of specific, important features of the clinical presentation or of the course, onset, and pattern of mood episodes. These categories are not mutually exclusive, and as many may be added as apply. Also known as: Symptomatic and course presentations for mood episodes in mood disorders [LA8C.1] Anomalous aortic origin or course of coronary artery Definition: A congenital cardiovascular malformation in which the origin and/or course of a coronary artery is abnormal. This is where coronary "anomalies" in the presence of discordant ventriculo-arterial connections should be coded. Also known as: Anomalous aortic origin or course of coronary artery | Anomalous aortic origin of coronary artery with ventriculo-arterial concordance | Anomalous aortic origin of coronary artery | AAOCA - [Anomalous aortic origin of coronary artery] | Right coronary artery from left aortic sinus with ventriculo-arterial concordance [8B22.Y] Other specified cerebrovascular disease Also known as: Other specified cerebrovascular disease | Posterior reversible encephalopathy | Multiple or bilateral precerebral artery syndromes | multiple or bilateral precerebral artery syndromes, course of resolution unspecified | precerebral artery insufficiency NOS [5C50.00] Classical phenylketonuria Definition: Classical phenylketonuria is a severe form of phenylketonuria (PKU) an inborn error of amino acid metabolism characterised in untreated patients by severe intellectual deficit and neuropsychiatric complications. Also known as: Classical phenylketonuria | phenylpyruvic oligophrenia | oligophrenia phenylpyruvica | imbecilitus phenylpyruvica | Typical phenylketonuria [1D40] Chikungunya virus disease Also known as: Chikungunya virus disease | Chikungunya fever | Chikungunya haemorrhagic fever | Chikungunya viral disease | Chikungunya mosquito-borne viral fever [8A68.2] Absence seizures, typical Definition: Seizures characterised by sudden onset, interruption of ongoing activities, blank stare, possibly brief upward gaze deviation, unresponsiveness, duration from few seconds to half a minute, and rapid recovery. An EEG would show generalised epileptiform discharges during the event. Also known as: Absence seizures, typical [8C72.00] Nemaline myopathy Definition: 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 (rods) on muscle biopsy. Also known as: Nemaline myopathy | rod myopathy | nemaline body disease | Adult-onset nemaline myopathy | Amish nemaline myopathy [DA90.0] Syndromic diarrhoea Definition: Syndromic diarrhoea (SD), also known as phenotypic diarrhoea (PD) or tricho-hepato-enteric syndrome (THE), is a congenital enteropathy presenting with early-onset of severe diarrhoea requiring parenteral nutrition (PN), associated with facial dysmorphism, woolly and poorly pigmented hair and liver disease, with extensive fibrosis or cirrhosis, in about half of the patients. Also known as: Syndromic diarrhoea | Phenotypic diarrhoea | THE - [tricho-hepato-enteric] syndrome Includes: Phenotypic diarrhoea === 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 cardiac tumor, not otherwise specified Def: A congenital malformation consisting of growth of abnormal tissue within the heart.... --- 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.... --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 3 --- [8B10.Y] Other specified transient ischaemic attack --PARENT--> [8B10] Transient ischaemic attack Def: Transient episode of focal neurological dysfunction caused by focal brain ischemia without acute infarction in the clinically relevant area of the brain or transient monocular visual loss due to retin... --CHILD--> [8B10.Y] Other specified transient ischaemic attack --- Walk 4 --- [8B10.Y] Other specified transient ischaemic attack --PARENT--> [8B10] Transient ischaemic attack Def: Transient episode of focal neurological dysfunction caused by focal brain ischemia without acute infarction in the clinically relevant area of the brain or transient monocular visual loss due to retin... --CHILD--> [8B10.Z] Transient ischaemic attack, unspecified --- Walk 5 --- [6A80] Symptomatic and course presentations for mood episodes in mood disorders Def: These categories may be applied to describe the presentation and characteristics of mood episodes in the context of single episode depressive disorder, recurrent depressive disorder, bipolar type I di... --CHILD--> [6A80.1] Panic attacks in mood episodes Def: In the context of a current mood episode (manic, depressive, mixed, or hypomanic), there have been recurrent panic attacks (i.e., at least two) during the past month that occur specifically in respons... --PARENT--> [6A80] Symptomatic and course presentations for mood episodes in mood disorders Def: These categories may be applied to describe the presentation and characteristics of mood episodes in the context of single episode depressive disorder, recurrent depressive disorder, bipolar type I di... --- Walk 6 --- [6A80] Symptomatic and course presentations for mood episodes in mood disorders Def: These categories may be applied to describe the presentation and characteristics of mood episodes in the context of single episode depressive disorder, recurrent depressive disorder, bipolar type I di... --CHILD--> [6A80.2] Current depressive episode persistent Def: The diagnostic requirements for a depressive episode are currently met and have been met continuously for at least the past 2 years.... --PARENT--> [6A80] Symptomatic and course presentations for mood episodes in mood disorders Def: These categories may be applied to describe the presentation and characteristics of mood episodes in the context of single episode depressive disorder, recurrent depressive disorder, bipolar type I di...
[ "[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....", "[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 --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....", "[8B10.Y] Other specified transient ischaemic attack\n --PARENT--> [8B10] Transient ischaemic attack\n Def: Transient episode of focal neurological dysfunction caused by focal brain ischemia without acute infarction in the clinically relevant area of the brain or transient monocular visual loss due to retin...\n --CHILD--> [8B10.Y] Other specified transient ischaemic attack", "[8B10.Y] Other specified transient ischaemic attack\n --PARENT--> [8B10] Transient ischaemic attack\n Def: Transient episode of focal neurological dysfunction caused by focal brain ischemia without acute infarction in the clinically relevant area of the brain or transient monocular visual loss due to retin...\n --CHILD--> [8B10.Z] Transient ischaemic attack, unspecified", "[6A80] Symptomatic and course presentations for mood episodes in mood disorders\n Def: These categories may be applied to describe the presentation and characteristics of mood episodes in the context of single episode depressive disorder, recurrent depressive disorder, bipolar type I di...\n --CHILD--> [6A80.1] Panic attacks in mood episodes\n Def: In the context of a current mood episode (manic, depressive, mixed, or hypomanic), there have been recurrent panic attacks (i.e., at least two) during the past month that occur specifically in respons...\n --PARENT--> [6A80] Symptomatic and course presentations for mood episodes in mood disorders\n Def: These categories may be applied to describe the presentation and characteristics of mood episodes in the context of single episode depressive disorder, recurrent depressive disorder, bipolar type I di...", "[6A80] Symptomatic and course presentations for mood episodes in mood disorders\n Def: These categories may be applied to describe the presentation and characteristics of mood episodes in the context of single episode depressive disorder, recurrent depressive disorder, bipolar type I di...\n --CHILD--> [6A80.2] Current depressive episode persistent\n Def: The diagnostic requirements for a depressive episode are currently met and have been met continuously for at least the past 2 years....\n --PARENT--> [6A80] Symptomatic and course presentations for mood episodes in mood disorders\n Def: These categories may be applied to describe the presentation and characteristics of mood episodes in the context of single episode depressive disorder, recurrent depressive disorder, bipolar type I di..." ]
LA8Y
Other specified structural developmental anomaly of heart or great vessels
[ { "from_icd11": "LA8Y", "icd10_code": "Q248 ", "icd10_title": "" }, { "from_icd11": "5C50.00", "icd10_code": "E700", "icd10_title": "Classical phenylketonuria" }, { "from_icd11": "1D40", "icd10_code": "A920", "icd10_title": "Chikungunya virus disease" }, { "from_icd11": "DA90.0", "icd10_code": "K529", "icd10_title": "Noninfective gastroenteritis and colitis, unspecified" } ]
Q248
WAS is a rare and potentially fatal disorder of X-linked recessive inheritance that is characterized by recurrent sinopulmonary infections, eczema, and microthrombocytopenia. We report here a young child with newly diagnosed WAS complicated by CMV, with clinical and laboratory findings similar to JMML. Yoshimi et al. reported seven infant boys with WAS who initially presented with leukocytosis, monocytosis, and myeloid and erythroid precursors in their peripheral blood as well as bone marrow dysplasia . The authors noted that the patients’ MPV values were normal or high, which is incompatible with WAS. As we observed in our case, this clinical picture is indistinguishable from JMML. Affected patients may have variable clinical presentations due to disease-modifying genetic factors and different exposure to pathogens . The causes of JMML-like features in WAS patients are poorly understood. Recent reports suggest that such atypical features may be attributed to coexistence of viral infection or activation of WAS protein by a somatic mutation concomitant with RAS pathway mutations . Based on these considerations, we believe that CMV infection was responsible for our patient developing a JMML-like clinical picture and immune cytopenia. Although JMML mutational studies were not performed, persistent monocytosis, splenomegaly, and positive PCR results for CMV all support the diagnosis of CMV infection.
4.210938
0.691895
sec[0]/p[2]
en
0.999997
29983408
https://doi.org/10.4274/tjh.galenos.2018.2018.0187
[ "jmml", "that", "patients", "infection", "monocytosis", "picture", "like", "features", "rare", "potentially" ]
[ { "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": "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 === [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 [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 --- [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... --CHILD--> [8A80.0] Migraine without aura Def: Recurrent headache disorder manifesting in attacks lasting 4-72 hours. The duration of attacks may be shorter in children. Typical characteristics of the headache are unilateral location, pulsating qu... --- 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... --CHILD--> [8A80.1] Migraine with aura Def: Recurrent attacks, lasting minutes, of unilateral fully-reversible visual, sensory or other central nervous system symptoms that usually develop gradually and are usually followed by headache and asso... --- 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--> [QA72] Incorrect substance without injury or harm Def: Incorrect substance administration occurs when a substance is given which was not the intended or prescribed drug and does not result in injury or harm.... --- 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--> [PL13.1] Underdosing, 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 --CHILD--> [8A80.0] Migraine without aura\n Def: Recurrent headache disorder manifesting in attacks lasting 4-72 hours. The duration of attacks may be shorter in children. Typical characteristics of the headache are unilateral location, pulsating qu...", "[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 --CHILD--> [8A80.1] Migraine with aura\n Def: Recurrent attacks, lasting minutes, of unilateral fully-reversible visual, sensory or other central nervous system symptoms that usually develop gradually and are usually followed by headache and asso...", "[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--> [QA72] Incorrect substance without injury or harm\n Def: Incorrect substance administration occurs when a substance is given which was not the intended or prescribed drug and does not result in 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", "[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--> [PL13.1] Underdosing, 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
After satisfactory general anesthesia, the patient was placed on cardiopulmonary bypass. With the heart completely decompressed, the lung was retracted. The anomalous vein was identified in an oblique fissure of the right lung and demonstrated to drain through the diaphragm. The anomalous vein was dissected for a distance of several centimeters from the diaphragm up and toward the hilum of the lung. The right atrium was opened through a longitudinal incision approximately 1.5 cm away from the AV groove. There was a large fossa ovalis and a small patent foramen ovale. These landmarks were used as guide for excising the entire fossa ovalis to a diameter of approximately 1.6 to 1.8 cm. A ribbed 16 mm Gore-Tex graft was chosen and sutured end-to-side to this newly created atrial septal defect with continuous 5-0 Prolene suture. A linear incision slightly smaller than the graft was made very low in the lateral right atrial wall, and the graft was brought through this defect and then through a defect in the pleura. A linear incision was made in the anomalous pulmonary vein, and the graft was sutured to this vein meticulously with a continuous 5-0 Prolene suture . After confirming both anastomosis and the patency of the graft, the anomalous vein was ligated between the Gore-Tex graft and the diaphragm. The patient tolerated the procedure well and was discharged on warfarin four days after the procedure.
3.865234
0.967285
sec[2]/p[0]
en
0.999999
31198608
https://doi.org/10.1155/2019/6932680
[ "graft", "vein", "anomalous", "lung", "diaphragm", "incision", "this", "defect", "approximately", "fossa" ]
[ { "code": "NE84", "title": "Failure or rejection of transplanted organs or tissues" }, { "code": "EL53", "title": "Skin graft failure" }, { "code": "EL54", "title": "Composite graft failure" }, { "code": "PK99.2", "title": "Orthopaedic devices associated with injury or harm, prosthetic or other implants, materials or accessory devices" }, { "code": "PK95.2Y", "title": "Other specified neurological devices associated with injury or harm, prosthetic or other implants, materials or accessory devices" }, { "code": "BD7Z", "title": "Diseases of veins, unspecified" }, { "code": "MC88", "title": "Prominent veins" }, { "code": "BD7Y", "title": "Other specified diseases of veins" }, { "code": "BD75.Y", "title": "Venous varicosities of other specified sites" }, { "code": "BD73.2Z", "title": "Systemic vein obstruction, unspecified" } ]
=== ICD-11 CODES FOUND === [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 [EL53] Skin graft failure Definition: Failure of skin graft tissue to engraft as intended Also known as: Skin graft failure | Split skin graft failure | Full thickness skin graft failure [EL54] Composite graft failure Definition: Failure of composite graft tissue (e.g. skin and cartilage) to engraft as intended Also known as: Composite graft failure [PK99.2] Orthopaedic devices associated with injury or harm, prosthetic or other implants, materials or accessory devices Definition: Orthopaedic related prosthetic and other implants, materials and accessory devices were involved in an adverse related incident Also known as: Orthopaedic devices associated with injury or harm, prosthetic or other implants, materials or accessory devices | Surgical operation with implant of artificial internal orthopaedic device associated with abnormal reaction of the patient, or of later complication, without mention of misadventure at the time of the procedure | Orthopaedic devices associated with injury or harm, limb prosthesis | Orthopaedic devices associated with injury or harm, joint prosthesis | Mechanical complication of internal joint prosthesis Excludes: Wear of articular bearing surface of joint prosthesis | Circumstances associated with a surgical or other medical device influencing the episode of care without injury or harm [PK95.2Y] Other specified neurological devices associated with injury or harm, prosthetic or other implants, materials or accessory devices Also known as: Other specified neurological devices associated with injury or harm, prosthetic or other implants, materials or accessory devices | Mechanical complication of nerve graft [BD7Z] Diseases of veins, unspecified Also known as: Diseases of veins, unspecified [MC88] Prominent veins Also known as: Prominent veins [BD7Y] Other specified diseases of veins Also known as: Other specified diseases of veins [BD75.Y] Venous varicosities of other specified sites Also known as: Venous varicosities of other specified sites | Caput medusae | Jugular venous aneurysm | jugular vein aneurysm | Orbital varices [BD73.2Z] Systemic vein obstruction, unspecified Also known as: Systemic vein obstruction, unspecified | Systemic vein obstruction === GRAPH WALKS === --- Walk 1 --- [NE84] Failure or rejection of transplanted organs or tissues --PARENT--> [?] Injury or harm arising from surgical or medical care, not elsewhere classified --EXCLUDES--> [?] Attention to artificial openings --- Walk 2 --- [NE84] Failure or rejection of transplanted organs or tissues --PARENT--> [?] Injury or harm arising from surgical or medical care, not elsewhere classified --EXCLUDES--> [?] Harmful effects of drugs, medicaments or biological substances, not elsewhere classified --- Walk 3 --- [EL53] Skin graft failure Def: Failure of skin graft tissue to engraft as intended... --PARENT--> [?] Postprocedural disorders of the skin Def: This group of disorders incorporates drug eruptions, other cutaneous side effects of medication and adverse reactions to medical and surgical interventions.... --CHILD--> [EL51] Cutaneous flap necrosis Def: Necrosis of surgical skin flap... --- Walk 4 --- [EL53] Skin graft failure Def: Failure of skin graft tissue to engraft as intended... --PARENT--> [?] Postprocedural disorders of the skin Def: This group of disorders incorporates drug eruptions, other cutaneous side effects of medication and adverse reactions to medical and surgical interventions.... --CHILD--> [EL50] Unsatisfactory surgical scar of skin Def: A surgical skin scar with a poor functional or cosmetic outcome.... --- Walk 5 --- [EL54] Composite graft failure Def: Failure of composite graft tissue (e.g. skin and cartilage) to engraft as intended... --PARENT--> [?] Postprocedural disorders of the skin Def: This group of disorders incorporates drug eruptions, other cutaneous side effects of medication and adverse reactions to medical and surgical interventions.... --CHILD--> [EL51] Cutaneous flap necrosis Def: Necrosis of surgical skin flap... --- Walk 6 --- [EL54] Composite graft failure Def: Failure of composite graft tissue (e.g. skin and cartilage) to engraft as intended... --PARENT--> [?] Postprocedural disorders of the skin Def: This group of disorders incorporates drug eruptions, other cutaneous side effects of medication and adverse reactions to medical and surgical interventions.... --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...
[ "[NE84] Failure or rejection of transplanted organs or tissues\n --PARENT--> [?] Injury or harm arising from surgical or medical care, not elsewhere classified\n --EXCLUDES--> [?] Attention to artificial openings", "[NE84] Failure or rejection of transplanted organs or tissues\n --PARENT--> [?] Injury or harm arising from surgical or medical care, not elsewhere classified\n --EXCLUDES--> [?] Harmful effects of drugs, medicaments or biological substances, not elsewhere classified", "[EL53] Skin graft failure\n Def: Failure of skin graft tissue to engraft as intended...\n --PARENT--> [?] Postprocedural disorders of the skin\n Def: This group of disorders incorporates drug eruptions, other cutaneous side effects of medication and adverse reactions to medical and surgical interventions....\n --CHILD--> [EL51] Cutaneous flap necrosis\n Def: Necrosis of surgical skin flap...", "[EL53] Skin graft failure\n Def: Failure of skin graft tissue to engraft as intended...\n --PARENT--> [?] Postprocedural disorders of the skin\n Def: This group of disorders incorporates drug eruptions, other cutaneous side effects of medication and adverse reactions to medical and surgical interventions....\n --CHILD--> [EL50] Unsatisfactory surgical scar of skin\n Def: A surgical skin scar with a poor functional or cosmetic outcome....", "[EL54] Composite graft failure\n Def: Failure of composite graft tissue (e.g. skin and cartilage) to engraft as intended...\n --PARENT--> [?] Postprocedural disorders of the skin\n Def: This group of disorders incorporates drug eruptions, other cutaneous side effects of medication and adverse reactions to medical and surgical interventions....\n --CHILD--> [EL51] Cutaneous flap necrosis\n Def: Necrosis of surgical skin flap...", "[EL54] Composite graft failure\n Def: Failure of composite graft tissue (e.g. skin and cartilage) to engraft as intended...\n --PARENT--> [?] Postprocedural disorders of the skin\n Def: This group of disorders incorporates drug eruptions, other cutaneous side effects of medication and adverse reactions to medical and surgical interventions....\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..." ]
NE84
Failure or rejection of transplanted organs or tissues
[ { "from_icd11": "NE84", "icd10_code": "T865", "icd10_title": "Complications of stem cell transplant" }, { "from_icd11": "NE84", "icd10_code": "T8649", "icd10_title": "Other complications of liver transplant" }, { "from_icd11": "NE84", "icd10_code": "T86891", "icd10_title": "Other transplanted tissue failure" }, { "from_icd11": "NE84", "icd10_code": "T86890", "icd10_title": "Other transplanted tissue rejection" }, { "from_icd11": "NE84", "icd10_code": "T86822", "icd10_title": "Skin graft (allograft) (autograft) infection" }, { "from_icd11": "NE84", "icd10_code": "T86828", "icd10_title": "Other complications of skin graft (allograft) (autograft)" }, { "from_icd11": "NE84", "icd10_code": "T8641", "icd10_title": "Liver transplant rejection" }, { "from_icd11": "NE84", "icd10_code": "T8642", "icd10_title": "Liver transplant failure" }, { "from_icd11": "NE84", "icd10_code": "T8613", "icd10_title": "Kidney transplant infection" }, { "from_icd11": "NE84", "icd10_code": "T8643", "icd10_title": "Liver transplant infection" }, { "from_icd11": "NE84", "icd10_code": "T86898", "icd10_title": "Other complications of other transplanted tissue" }, { "from_icd11": "NE84", "icd10_code": "T86821", "icd10_title": "Skin graft (allograft) (autograft) failure" }, { "from_icd11": "NE84", "icd10_code": "T8621", "icd10_title": "Heart transplant rejection" }, { "from_icd11": "NE84", "icd10_code": "T8622", "icd10_title": "Heart transplant failure" }, { "from_icd11": "NE84", "icd10_code": "T86892", "icd10_title": "Other transplanted tissue infection" } ]
T865
Complications of stem cell transplant
For her presenting symptoms, she was previously evaluated for genetic abnormalities at an outside facility in 2021, where vitamin B6 levels of 301.3 nmol/L and 202.6 nmol/L (reference range, 20-125 nmol/L) approximately 5 months apart were reported. Additionally, in 2021, her total ALP levels were 50 U/L in January, 36 U/L in March, and 56 U/L in July, all within the normal limits of 31 to 125 U/L. Her ALP levels in 2017 and 2020 were 34 U/L and 43 U/L, respectively ( Table ). In 2022, she underwent a bone dual-energy x-ray absorptiometry examination at an outside facility to evaluate for low bone mass. Her dual-energy x-ray absorptiometry scan was within normal limits, with a T-score of 1.2 in the L1 to L3 region, a T-score of 1.3 in the left femoral neck, a T-score of 1.4 in the total left femur, a T-score of 0.9 in the right femoral neck, and a T-score of 1.1 in the total right femur. Table Patient Laboratory values Date Alkaline phosphatase, total (reference range, 31-125 U/L) Alkaline phosphatase, bone-specific (reference range, 5.3-19.5 μg/L) Vitamin B6 (reference range, 2.1-21.7 ng/mL, 20-125 nmol/L a ) February 2023 60 U/L 4.4 μg/L 43.9 ng/mL July 2021 56 U/L … 202.6 nmol/L a March 2021 36 U/L … … January 2021 50 U/L … 301.3 nmol/L a May 2020 43 U/L … … December 2018 54 U/L … … November 2017 34 U/L … … a Different units recorded due to being performed and reported from an outside facility
3.96875
0.900879
sec[1]/p[1]
en
0.999998
PMC10958627
https://doi.org/10.1016/j.aace.2023.11.006
[ "nmol", "score", "reference", "range", "total", "outside", "facility", "bone", "vitamin", "january" ]
[ { "code": "MB20.1&XC87", "title": "Glasgow Coma Scale, eyes opening, never" }, { "code": "KD30.0", "title": "Birth depression with 5 minute Apgar score 0-3" }, { "code": "KD30.1", "title": "Birth depression with 5 minute Apgar score 4-6" }, { "code": "MB20.1", "title": "Coma" }, { "code": "KB21.0", "title": "Severe birth asphyxia" }, { "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" } ]
=== ICD-11 CODES FOUND === [KD30.0] Birth depression with 5 minute Apgar score 0-3 Definition: A condition characterised by cardiorespiratory and neurological depression, defined as an Apgar score between 0 to 3 at 5 minutes following birth. Also known as: Birth depression with 5 minute Apgar score 0-3 [KD30.1] Birth depression with 5 minute Apgar score 4-6 Definition: A condition characterised by cardiorespiratory and neurological depression, defined as an Apgar score between 4 and 6 at 5 minutes following birth. Also known as: Birth depression with 5 minute Apgar score 4-6 [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 [KB21.0] Severe birth asphyxia Definition: Pulse less than 100 per minute at birth and falling or steady, respiration absent or gasping, colour poor, tone absent. Also known as: Severe birth asphyxia | severe perinatal hypoxia | asphyxia pallida of newborn | Asphyxia with 5-minute Apgar score 0-3 | newborn severe asphyxia [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 === GRAPH WALKS === --- Walk 1 --- [KD30.0] Birth depression with 5 minute Apgar score 0-3 Def: A condition characterised by cardiorespiratory and neurological depression, defined as an Apgar score between 0 to 3 at 5 minutes following birth.... --PARENT--> [KD30] Birth depression Def: A condition characterised by cardiorespiratory and neurological depression in a newborn.... --CHILD--> [KD30.1] Birth depression with 5 minute Apgar score 4-6 Def: A condition characterised by cardiorespiratory and neurological depression, defined as an Apgar score between 4 and 6 at 5 minutes following birth.... --- Walk 2 --- [KD30.0] Birth depression with 5 minute Apgar score 0-3 Def: A condition characterised by cardiorespiratory and neurological depression, defined as an Apgar score between 0 to 3 at 5 minutes following birth.... --PARENT--> [KD30] Birth depression Def: A condition characterised by cardiorespiratory and neurological depression in a newborn.... --CHILD--> [KD30.1] Birth depression with 5 minute Apgar score 4-6 Def: A condition characterised by cardiorespiratory and neurological depression, defined as an Apgar score between 4 and 6 at 5 minutes following birth.... --- Walk 3 --- [KD30.1] Birth depression with 5 minute Apgar score 4-6 Def: A condition characterised by cardiorespiratory and neurological depression, defined as an Apgar score between 4 and 6 at 5 minutes following birth.... --PARENT--> [KD30] Birth depression Def: A condition characterised by cardiorespiratory and neurological depression in a newborn.... --CHILD--> [KD30.1] Birth depression with 5 minute Apgar score 4-6 Def: A condition characterised by cardiorespiratory and neurological depression, defined as an Apgar score between 4 and 6 at 5 minutes following birth.... --- Walk 4 --- [KD30.1] Birth depression with 5 minute Apgar score 4-6 Def: A condition characterised by cardiorespiratory and neurological depression, defined as an Apgar score between 4 and 6 at 5 minutes following birth.... --PARENT--> [KD30] Birth depression Def: A condition characterised by cardiorespiratory and neurological depression in a newborn.... --CHILD--> [KD30.1] Birth depression with 5 minute Apgar score 4-6 Def: A condition characterised by cardiorespiratory and neurological depression, defined as an Apgar score between 4 and 6 at 5 minutes following birth.... --- Walk 5 --- [MB20.1] Coma Def: 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. Mot... --EXCLUDES--> [?] Neonatal encephalopathy, severe Def: A paediatric condition characterised by a newborn who does not open their eyes even in response to pain or noise, who does not respond verbally or who is inconsolable, and who either has an inappropri... --EXCLUDES--> [?] Hypoxic ischaemic encephalopathy of newborn Def: Hypoxic ischaemic encephalopathy (HIE) is when a newborn’s brain fails to receive a sufficient amount of oxygen or blood before and during birth that may lead to brain damage or death.... --- Walk 6 --- [MB20.1] Coma Def: 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. Mot... --EXCLUDES--> [?] Neonatal encephalopathy, severe Def: A paediatric condition characterised by a newborn who does not open their eyes even in response to pain or noise, who does not respond verbally or who is inconsolable, and who either has an inappropri... --EXCLUDES--> [?] Hypoxic ischaemic encephalopathy of newborn Def: Hypoxic ischaemic encephalopathy (HIE) is when a newborn’s brain fails to receive a sufficient amount of oxygen or blood before and during birth that may lead to brain damage or death....
[ "[KD30.0] Birth depression with 5 minute Apgar score 0-3\n Def: A condition characterised by cardiorespiratory and neurological depression, defined as an Apgar score between 0 to 3 at 5 minutes following birth....\n --PARENT--> [KD30] Birth depression\n Def: A condition characterised by cardiorespiratory and neurological depression in a newborn....\n --CHILD--> [KD30.1] Birth depression with 5 minute Apgar score 4-6\n Def: A condition characterised by cardiorespiratory and neurological depression, defined as an Apgar score between 4 and 6 at 5 minutes following birth....", "[KD30.0] Birth depression with 5 minute Apgar score 0-3\n Def: A condition characterised by cardiorespiratory and neurological depression, defined as an Apgar score between 0 to 3 at 5 minutes following birth....\n --PARENT--> [KD30] Birth depression\n Def: A condition characterised by cardiorespiratory and neurological depression in a newborn....\n --CHILD--> [KD30.1] Birth depression with 5 minute Apgar score 4-6\n Def: A condition characterised by cardiorespiratory and neurological depression, defined as an Apgar score between 4 and 6 at 5 minutes following birth....", "[KD30.1] Birth depression with 5 minute Apgar score 4-6\n Def: A condition characterised by cardiorespiratory and neurological depression, defined as an Apgar score between 4 and 6 at 5 minutes following birth....\n --PARENT--> [KD30] Birth depression\n Def: A condition characterised by cardiorespiratory and neurological depression in a newborn....\n --CHILD--> [KD30.1] Birth depression with 5 minute Apgar score 4-6\n Def: A condition characterised by cardiorespiratory and neurological depression, defined as an Apgar score between 4 and 6 at 5 minutes following birth....", "[KD30.1] Birth depression with 5 minute Apgar score 4-6\n Def: A condition characterised by cardiorespiratory and neurological depression, defined as an Apgar score between 4 and 6 at 5 minutes following birth....\n --PARENT--> [KD30] Birth depression\n Def: A condition characterised by cardiorespiratory and neurological depression in a newborn....\n --CHILD--> [KD30.1] Birth depression with 5 minute Apgar score 4-6\n Def: A condition characterised by cardiorespiratory and neurological depression, defined as an Apgar score between 4 and 6 at 5 minutes following birth....", "[MB20.1] Coma\n Def: 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. Mot...\n --EXCLUDES--> [?] Neonatal encephalopathy, severe\n Def: A paediatric condition characterised by a newborn who does not open their eyes even in response to pain or noise, who does not respond verbally or who is inconsolable, and who either has an inappropri...\n --EXCLUDES--> [?] Hypoxic ischaemic encephalopathy of newborn\n Def: Hypoxic ischaemic encephalopathy (HIE) is when a newborn’s brain fails to receive a sufficient amount of oxygen or blood before and during birth that may lead to brain damage or death....", "[MB20.1] Coma\n Def: 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. Mot...\n --EXCLUDES--> [?] Neonatal encephalopathy, severe\n Def: A paediatric condition characterised by a newborn who does not open their eyes even in response to pain or noise, who does not respond verbally or who is inconsolable, and who either has an inappropri...\n --EXCLUDES--> [?] Hypoxic ischaemic encephalopathy of newborn\n Def: Hypoxic ischaemic encephalopathy (HIE) is when a newborn’s brain fails to receive a sufficient amount of oxygen or blood before and during birth that may lead to brain damage or death...." ]
MB20.1&XC87
Glasgow Coma Scale, eyes opening, never
[ { "from_icd11": "KD30.0", "icd10_code": "P210", "icd10_title": "" }, { "from_icd11": "KD30.1", "icd10_code": "P211", "icd10_title": "" }, { "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" }, { "from_icd11": "MB20.1", "icd10_code": "R402363", "icd10_title": "Coma scale, best motor response, obeys commands, at hospital admission" }, { "from_icd11": "MB20.1", "icd10_code": "R402433", "icd10_title": "Glasgow coma scale score 3-8, at hospital admission" } ]
P210
We report the case of a previously well 18-year-old Sri Lankan Sinhalese boy, resident of a dengue endemic area, who presented with a 1-day history of high fever and tonic-clonic movements of the left upper and lower limbs later converting into a generalized tonic-clonic (GTC) seizure to the Teaching Hospital Peradeniya, Sri Lanka. The fever was high grade without chills but associated with arthralgia, myalgia, headache, and vomiting. The seizures commenced on the evening of the first day of the illness, lasted for 10 minutes and were associated with postictal drowsiness. A persistent left-sided face, arm, and leg weakness was apparent as the postictal drowsiness improved. There were no associated sensory symptoms and the weakness was more pronounced in his face and upper limb. There was no associated abdominal pain, postural dizziness, reduced urine output, or any bleeding tendency. There was no recent history of vaccination and no skin rashes. He had been investigated following a head injury 10 months back. He presented after a road traffic accident with mild drowsiness without any focal neurological weakness and a non-contrast computed tomography (NCCT) scan of his brain had been normal. He was completely well on discharge and no long-term neurological symptoms were evident until this incident. His past medical history was unremarkable with no history of epilepsy or collagen vascular diseases.
3.896484
0.984375
sec[1]/p[0]
en
0.999997
31488206
https://doi.org/10.1186/s13256-019-2201-x
[ "associated", "drowsiness", "weakness", "well", "fever", "tonic", "clonic", "without", "postictal", "face" ]
[ { "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" }, { "code": "MG42", "title": "Somnolence, not elsewhere classified" }, { "code": "MG22", "title": "Fatigue" }, { "code": "FB32.Y", "title": "Other specified disorders of muscles" }, { "code": "MB5Z", "title": "Paralytic symptoms, unspecified" }, { "code": "FA31.5", "title": "Acquired pes planus" } ]
=== ICD-11 CODES FOUND === [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 [MG42] Somnolence, not elsewhere classified Also known as: Somnolence, not elsewhere classified | Drowsiness | somnolence NEC Includes: Drowsiness Excludes: Sleep-wake disorders [MG22] Fatigue Definition: A feeling of exhaustion, lethargy, or decreased energy, usually experienced as a weakening or depletion of one's physical or mental resource and characterised by a decreased capacity for work and reduced efficiency in responding to stimuli. Fatigue is normal following a period of exertion, mental or physical, but sometimes may occur in the absence of such exertion as a symptom of health conditions. Also known as: Fatigue | decreased energy | worn out | Lethargy | lethargic Includes: General physical deterioration | Lethargy Excludes: Combat fatigue | Exhaustion due to exposure | heat exhaustion [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 [MB5Z] Paralytic symptoms, unspecified Also known as: Paralytic symptoms, unspecified | paralysis syndrome | incomplete paralysis | complete paralysis | paresis [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 === GRAPH WALKS === --- Walk 1 --- [MB25.02] Disorganised thinking Def: 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 i... --PARENT--> [MB25.0] Symptoms or signs of thought disorder Def: Disturbances in the associative thought process typically manifest in speech or writing that range from circumstantiality to incoherence. These may be indicative of Schizophrenia and other primary psy... --CHILD--> [MB25.02] Disorganised thinking Def: 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 i... --- Walk 2 --- [MB25.02] Disorganised thinking Def: 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 i... --PARENT--> [MB25.0] Symptoms or signs of thought disorder Def: Disturbances in the associative thought process typically manifest in speech or writing that range from circumstantiality to incoherence. These may be indicative of Schizophrenia and other primary psy... --CHILD--> [MB25.01] Tangentiality Def: A disturbance in the associative thought process typically manifest in speech in which the person tends to digress readily from the topic under discussion to other topics through associations without ... --- Walk 3 --- [LD2F.11] VATER association Def: 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-oesoph... --PARENT--> [LD2F.1] Syndromes with multiple structural anomalies, not of environmental origin --CHILD--> [LD2F.12] Sirenomelia Def: Sirenomelia is a rare lethal malformation characterised by severe anomalies of the caudal part of the fetus that include a single lower limb, with various degrees of involvement ranging from single to... --- Walk 4 --- [LD2F.11] VATER association Def: 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-oesoph... --PARENT--> [LD2F.1] Syndromes with multiple structural anomalies, not of environmental origin --RELATED_TO--> [?] Oculocerebrorenal syndrome Def: Oculocerebrorenal syndrome of Lowe (OCRL) is a multisystem disorder characterised by congenital cataracts, glaucoma, intellectual disabilities, postnatal growth retardation and renal tubular dysfuncti... --- Walk 5 --- [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--> [?] Prader-Willi syndrome Def: Prader-Willi syndrome is a rare genetic disorder characterised by hypothalamic-pituitary abnormalities with severe hypotonia during the neonatal period and first two years of life and the onset of hyp... --PARENT--> [?] Syndromes with obesity as a major feature --- Walk 6 --- [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--> [?] Prader-Willi syndrome Def: Prader-Willi syndrome is a rare genetic disorder characterised by hypothalamic-pituitary abnormalities with severe hypotonia during the neonatal period and first two years of life and the onset of hyp... --PARENT--> [?] Syndromes with obesity as a major feature
[ "[MB25.02] Disorganised thinking\n Def: 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 i...\n --PARENT--> [MB25.0] Symptoms or signs of thought disorder\n Def: Disturbances in the associative thought process typically manifest in speech or writing that range from circumstantiality to incoherence. These may be indicative of Schizophrenia and other primary psy...\n --CHILD--> [MB25.02] Disorganised thinking\n Def: 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 i...", "[MB25.02] Disorganised thinking\n Def: 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 i...\n --PARENT--> [MB25.0] Symptoms or signs of thought disorder\n Def: Disturbances in the associative thought process typically manifest in speech or writing that range from circumstantiality to incoherence. These may be indicative of Schizophrenia and other primary psy...\n --CHILD--> [MB25.01] Tangentiality\n Def: A disturbance in the associative thought process typically manifest in speech in which the person tends to digress readily from the topic under discussion to other topics through associations without ...", "[LD2F.11] VATER association\n Def: 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-oesoph...\n --PARENT--> [LD2F.1] Syndromes with multiple structural anomalies, not of environmental origin\n --CHILD--> [LD2F.12] Sirenomelia\n Def: Sirenomelia is a rare lethal malformation characterised by severe anomalies of the caudal part of the fetus that include a single lower limb, with various degrees of involvement ranging from single to...", "[LD2F.11] VATER association\n Def: 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-oesoph...\n --PARENT--> [LD2F.1] Syndromes with multiple structural anomalies, not of environmental origin\n --RELATED_TO--> [?] Oculocerebrorenal syndrome\n Def: Oculocerebrorenal syndrome of Lowe (OCRL) is a multisystem disorder characterised by congenital cataracts, glaucoma, intellectual disabilities, postnatal growth retardation and renal tubular dysfuncti...", "[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--> [?] Prader-Willi syndrome\n Def: Prader-Willi syndrome is a rare genetic disorder characterised by hypothalamic-pituitary abnormalities with severe hypotonia during the neonatal period and first two years of life and the onset of hyp...\n --PARENT--> [?] Syndromes with obesity as a major feature", "[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--> [?] Prader-Willi syndrome\n Def: Prader-Willi syndrome is a rare genetic disorder characterised by hypothalamic-pituitary abnormalities with severe hypotonia during the neonatal period and first two years of life and the onset of hyp...\n --PARENT--> [?] Syndromes with obesity as a major feature" ]
MB25.02
Disorganised thinking
[ { "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" }, { "from_icd11": "5A61.0", "icd10_code": "E231", "icd10_title": "Drug-induced hypopituitarism" }, { "from_icd11": "FB1Z", "icd10_code": "M435X2", "icd10_title": "Other recurrent vertebral dislocation, cervical region" }, { "from_icd11": "FB1Z", "icd10_code": "M438X4", "icd10_title": "Other specified deforming dorsopathies, thoracic region" }, { "from_icd11": "FB1Z", "icd10_code": "M4324", "icd10_title": "Fusion of spine, thoracic region" }, { "from_icd11": "FB1Z", "icd10_code": "M4325", "icd10_title": "Fusion of spine, thoracolumbar region" }, { "from_icd11": "FB1Z", "icd10_code": "M438X6", "icd10_title": "Other specified deforming dorsopathies, lumbar region" }, { "from_icd11": "FB1Z", "icd10_code": "M4320", "icd10_title": "Fusion of spine, site unspecified" }, { "from_icd11": "FB1Z", "icd10_code": "M438X7", "icd10_title": "Other specified deforming dorsopathies, lumbosacral region" }, { "from_icd11": "FB1Z", "icd10_code": "M438X5", "icd10_title": "Other specified deforming dorsopathies, thoracolumbar region" } ]
R4689
Other symptoms and signs involving appearance and behavior
In a second young woman with a lack of bone support for mentalis , distortion of the chin is evident both at rest and when she purses her lips . Immediately after treatment, improvement in her chin is observed at rest and on animation . Blocking the excessive movement of mentalis eliminates the resulting distortion and allows the patient to purse her lips with no skin wrinkling. Fig. 5 Case 4: Voluma was injected into the labiomental angle at the subcutaneous layer, superficial to depressor anguli oris and depressor labii inferioris (1.0 mL per side). Voluma was also injected at the chin apex into the deep fibers of mentalis (0.5 mL per side) using a 25-g cannula in a fanning pattern, and in a bolus pattern using a 27-g needle to reach the supraperiosteal level (0.3 mL per side). a Muscles involved. b Injection sites (blue markings; dot = bolus injection, bar = fanning). c At rest. Before treatment (left), wrinkling of the chin is evident at rest. Improvement in the chin is observed immediately after injection of Voluma in the labiomental angle and chin apex. d Purse (kiss). Before treatment (left), distortion of mentalis muscle during contraction as the patient purses her lips causes extreme wrinkling of the skin on the chin. After providing a mechanical block of mentalis muscle movement with Voluma injected in the labiomental angle and chin apex, the distortion and skin wrinkling are eliminated
4.023438
0.94873
sec[2]/p[6]
en
0.999995
29549406
https://doi.org/10.1007/s00266-018-1116-z
[ "chin", "mentalis", "distortion", "rest", "wrinkling", "voluma", "lips", "skin", "injected", "labiomental" ]
[ { "code": "NA0Z&XA2C62", "title": "Injury of chin" }, { "code": "JB04.2", "title": "Obstructed labour due to face presentation" }, { "code": "PK9B.2", "title": "General or plastic surgery devices associated with injury or harm, prosthetic or other implants, materials or accessory devices" }, { "code": "8A04.Y", "title": "Other specified disorders associated with tremor" }, { "code": "NE83.1", "title": "Infection arising from device, implant or graft, not elsewhere classified" }, { "code": "LB16.Z", "title": "Structural developmental anomalies of large intestine, unspecified" }, { "code": "9A24.Z", "title": "Bony deformity of orbit, unspecified" }, { "code": "LB20.23", "title": "Structural developmental anomalies of cystic duct" }, { "code": "LB20.2Z", "title": "Structural developmental anomalies of bile ducts, unspecified" }, { "code": "LA14.2", "title": "Structural developmental anomalies of orbit" } ]
=== ICD-11 CODES FOUND === [JB04.2] Obstructed labour due to face presentation Also known as: Obstructed labour due to face presentation | Labour and delivery affected by face presentation | Obstructed labour due to chin presentation [PK9B.2] General or plastic surgery devices associated with injury or harm, prosthetic or other implants, materials or accessory devices Definition: General- or plastic-surgery related prosthetic and other implants, materials and accessory devices were involved in an adverse related incident Also known as: General or plastic surgery devices associated with injury or harm, prosthetic or other implants, materials or accessory devices | Surgical operation with implant of artificial internal general or plastic surgery device associated with abnormal reaction of the patient, or of later complication, without mention of misadventure at the time of the procedure | General or plastic surgery devices associated with injury or harm, breast implant | General or plastic surgery devices associated with adverse incidents, breast implant | Mechanical complication of breast prosthesis and implant Excludes: Circumstances associated with a surgical or other medical device influencing the episode of care without injury or harm [8A04.Y] Other specified disorders associated with tremor Also known as: Other specified disorders associated with tremor | Other rhythmic disorders | Palatal tremor | Dystonic tremor | Rhythmic myoclonus [NE83.1] Infection arising from device, implant or graft, not elsewhere classified Also known as: Infection arising from device, implant or graft, not elsewhere classified | Infection or inflammatory reaction due to other cardiac and vascular devices, implants and grafts NOS | Infection or inflammation of artificial heart NOS | Infection or inflammation of vascular balloon implant or device NOS | Infection or inflammatory reaction of heart valve prosthesis NOS [LB16.Z] Structural developmental anomalies of large intestine, unspecified Also known as: Structural developmental anomalies of large intestine, unspecified | Structural developmental anomalies of large intestine | Malformation of large intestine | colon maldevelopment | bowel distortion NOS [9A24.Z] Bony deformity of orbit, unspecified Also known as: Bony deformity of orbit, unspecified | Bony deformity of orbit | distortion of orbit | Posttrauma deformity of orbit | posttrauma distortion of orbit [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 [LB20.2Z] Structural developmental anomalies of bile ducts, unspecified Also known as: Structural developmental anomalies of bile ducts, unspecified | Structural developmental anomalies of bile ducts | bile duct deformity | bile duct anomaly | bile duct distortion [LA14.2] Structural developmental anomalies of orbit Definition: Any condition caused by failure of the orbit to correctly develop during the antenatal period. Also known as: Structural developmental anomalies of orbit | congenital anomaly of orbit | congenital anomaly of orbit proper | specified congenital anomalies of orbit | anomaly of orbit === GRAPH WALKS === --- Walk 1 --- [JB04.2] Obstructed labour due to face presentation --PARENT--> [JB04] Obstructed labour due to malposition or malpresentation of fetus Def: A condition affecting pregnant females, caused by the abnormal position of fetal head or the abnormal presentation of the fetus away from the fetal head in vertex.... --CHILD--> [JB04.1] Obstructed labour due to breech presentation --- Walk 2 --- [JB04.2] Obstructed labour due to face presentation --PARENT--> [JB04] Obstructed labour due to malposition or malpresentation of fetus Def: A condition affecting pregnant females, caused by the abnormal position of fetal head or the abnormal presentation of the fetus away from the fetal head in vertex.... --PARENT--> [?] Complications of labour or delivery Def: Any complication characterised by the adverse evolution of a condition that arises during any one of the three stages of labour and delivery.... --- Walk 3 --- [PK9B.2] General or plastic surgery devices associated with injury or harm, prosthetic or other implants, materials or accessory devices Def: General- or plastic-surgery related prosthetic and other implants, materials and accessory devices 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.... --- Walk 4 --- [PK9B.2] General or plastic surgery devices associated with injury or harm, prosthetic or other implants, materials or accessory devices Def: General- or plastic-surgery related prosthetic and other implants, materials and accessory devices were involved in an adverse related incident... --PARENT--> [PK9B] General or plastic surgery devices, implants or grafts associated with injury or harm --CHILD--> [PK9B.2] General or plastic surgery devices associated with injury or harm, prosthetic or other implants, materials or accessory devices Def: General- or plastic-surgery related prosthetic and other implants, materials and accessory devices were involved in an adverse related incident... --- Walk 5 --- [8A04.Y] Other specified disorders associated with tremor --PARENT--> [8A04] Disorders associated with tremor Def: Tremor is an involuntary oscillation of a body part and is commonly classified according to the behavioural circumstances in which it occurs. Tremor may occur during attempted relaxation (rest tremor)... --CHILD--> [8A04.0] Enhanced physiological tremor Def: This is a high frequency, low amplitude tremor present with posture or action. It represents an exacerbation of a physiologic tremor which may have been worsened by drugs, stress, anxiety, etc.... --- Walk 6 --- [8A04.Y] Other specified disorders associated with tremor --PARENT--> [8A04] Disorders associated with tremor Def: Tremor is an involuntary oscillation of a body part and is commonly classified according to the behavioural circumstances in which it occurs. Tremor may occur during attempted relaxation (rest tremor)... --CHILD--> [8A04.2] Rest tremor Def: Resting tremors happen while the patient is sitting or lying down and relaxed. People who have a resting tremor can usually stop the tremor by deliberately moving the affected body part. It usually oc...
[ "[JB04.2] Obstructed labour due to face presentation\n --PARENT--> [JB04] Obstructed labour due to malposition or malpresentation of fetus\n Def: A condition affecting pregnant females, caused by the abnormal position of fetal head or the abnormal presentation of the fetus away from the fetal head in vertex....\n --CHILD--> [JB04.1] Obstructed labour due to breech presentation", "[JB04.2] Obstructed labour due to face presentation\n --PARENT--> [JB04] Obstructed labour due to malposition or malpresentation of fetus\n Def: A condition affecting pregnant females, caused by the abnormal position of fetal head or the abnormal presentation of the fetus away from the fetal head in vertex....\n --PARENT--> [?] Complications of labour or delivery\n Def: Any complication characterised by the adverse evolution of a condition that arises during any one of the three stages of labour and delivery....", "[PK9B.2] General or plastic surgery devices associated with injury or harm, prosthetic or other implants, materials or accessory devices\n Def: General- or plastic-surgery related prosthetic and other implants, materials and accessory devices 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....", "[PK9B.2] General or plastic surgery devices associated with injury or harm, prosthetic or other implants, materials or accessory devices\n Def: General- or plastic-surgery related prosthetic and other implants, materials and accessory devices were involved in an adverse related incident...\n --PARENT--> [PK9B] General or plastic surgery devices, implants or grafts associated with injury or harm\n --CHILD--> [PK9B.2] General or plastic surgery devices associated with injury or harm, prosthetic or other implants, materials or accessory devices\n Def: General- or plastic-surgery related prosthetic and other implants, materials and accessory devices were involved in an adverse related incident...", "[8A04.Y] Other specified disorders associated with tremor\n --PARENT--> [8A04] Disorders associated with tremor\n Def: Tremor is an involuntary oscillation of a body part and is commonly classified according to the behavioural circumstances in which it occurs. Tremor may occur during attempted relaxation (rest tremor)...\n --CHILD--> [8A04.0] Enhanced physiological tremor\n Def: This is a high frequency, low amplitude tremor present with posture or action. It represents an exacerbation of a physiologic tremor which may have been worsened by drugs, stress, anxiety, etc....", "[8A04.Y] Other specified disorders associated with tremor\n --PARENT--> [8A04] Disorders associated with tremor\n Def: Tremor is an involuntary oscillation of a body part and is commonly classified according to the behavioural circumstances in which it occurs. Tremor may occur during attempted relaxation (rest tremor)...\n --CHILD--> [8A04.2] Rest tremor\n Def: Resting tremors happen while the patient is sitting or lying down and relaxed. People who have a resting tremor can usually stop the tremor by deliberately moving the affected body part. It usually oc..." ]
NA0Z&XA2C62
Injury of chin
[ { "from_icd11": "JB04.2", "icd10_code": "O642XX0", "icd10_title": "Obstructed labor due to face presentation, not applicable or unspecified" }, { "from_icd11": "JB04.2", "icd10_code": "O642", "icd10_title": "Obstructed labor due to face presentation" }, { "from_icd11": "PK9B.2", "icd10_code": "T8549XA", "icd10_title": "Other mechanical complication of breast prosthesis and implant, initial encounter" }, { "from_icd11": "PK9B.2", "icd10_code": "T8543XA", "icd10_title": "Leakage of breast prosthesis and implant, initial encounter" }, { "from_icd11": "PK9B.2", "icd10_code": "T8544XA", "icd10_title": "Capsular contracture of breast implant, initial encounter" }, { "from_icd11": "PK9B.2", "icd10_code": "T8544XS", "icd10_title": "Capsular contracture of breast implant, sequela" }, { "from_icd11": "PK9B.2", "icd10_code": "T8542XA", "icd10_title": "Displacement of breast prosthesis and implant, initial encounter" }, { "from_icd11": "PK9B.2", "icd10_code": "T8541XA", "icd10_title": "Breakdown (mechanical) of breast prosthesis and implant, initial encounter" }, { "from_icd11": "PK9B.2", "icd10_code": "Y831", "icd10_title": "Surgical operation with implant of artificial internal device 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": "PK9B.2", "icd10_code": "Y812", "icd10_title": "Prosthetic and other implants, materials and accessory general- and plastic-surgery devices associated with adverse incidents" }, { "from_icd11": "PK9B.2", "icd10_code": "T854", "icd10_title": "Mechanical complication of breast prosthesis and implant" }, { "from_icd11": "NE83.1", "icd10_code": "T8359XA", "icd10_title": "" }, { "from_icd11": "NE83.1", "icd10_code": "T8453XD", "icd10_title": "Infection and inflammatory reaction due to internal right knee prosthesis, subsequent encounter" }, { "from_icd11": "NE83.1", "icd10_code": "T826XXA", "icd10_title": "Infection and inflammatory reaction due to cardiac valve prosthesis, initial encounter" }, { "from_icd11": "NE83.1", "icd10_code": "T84622A", "icd10_title": "Infection and inflammatory reaction due to internal fixation device of right tibia, initial encounter" } ]
O642XX0
Obstructed labor due to face presentation, not applicable or unspecified
Prior to presentation, Laura’s medical work-up showed focal chronic-type peptic duodenitis and reflux esophagitis. She was diagnosed with significant gluten sensitivity/intolerance, with a likely diagnosis of celiac disease. Laura had also been participating in weekly, individual play-based therapy for approximately 4 months to address her separation and other anxiety symptoms, without improvement. Her therapist did not have any expertise or experience in treating ARFID, therefore she was not focusing on weight regain or fears about eating. Laura was started on 20 mg of sertraline (liquid concentrate) 3 months prior to presentation at our service, though family had not seen any notable gains. Upon initial presentation to our team, Laura required hospitalization for 12 days for medical stabilization due to: symptomatic orthostasis, bradycardia, and severe malnutrition. During her hospital stay, Laura was diagnosed with ARFID, her sertraline was increased to 50 mg, and she was started on hydroxyzine, 5 mg TID to target pre-meal anxiety, nausea, and fullness. Following medical stabilization, Laura then began weekly outpatient treatment with her family to address the need for continued weight regain, anxiety/fears with eating, and separation anxiety. Given Laura had previously trended at or above the 85th percentile for BMI, the goal was to return her weight back to her personal healthy weight range.
3.609375
0.980469
sec[1]/p[1]
en
0.999997
31666952
https://doi.org/10.1186/s40337-019-0267-x
[ "laura", "anxiety", "weight", "diagnosed", "weekly", "address", "separation", "arfid", "regain", "fears" ]
[ { "code": "MB24.3", "title": "Anxiety" }, { "code": "6B00", "title": "Generalised anxiety disorder" }, { "code": "6E63", "title": "Secondary anxiety syndrome" }, { "code": "6B23.Z", "title": "Hypochondriasis, unspecified" }, { "code": "6B04", "title": "Social anxiety disorder" }, { "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" }, { "code": "JA65.2", "title": "Excessive weight gain in pregnancy" } ]
=== ICD-11 CODES FOUND === [MB24.3] Anxiety Definition: Apprehensiveness or anticipation of future danger or misfortune accompanied by a feeling of worry, distress, or somatic symptoms of tension. The focus of anticipated danger may be internal or external. Also known as: Anxiety | Nervous tension | nervous | Nervousness | nervous irritation Includes: Nervous tension [6B00] Generalised anxiety disorder Definition: Generalised anxiety disorder is characterised by marked symptoms of anxiety that persist for at least several months, for more days than not, manifested by either general apprehension (i.e. ‘free-floating anxiety’) or excessive worry focused on multiple everyday events, most often concerning family, health, finances, and school or work, together with additional symptoms such as muscular tension or motor restlessness, sympathetic autonomic over-activity, subjective experience of nervousness, diff Also known as: Generalised anxiety disorder | GAD - [generalised anxiety disorder] | anxiety generalised | Anxiety neurosis | neurotic anxiety [6E63] Secondary anxiety syndrome Definition: A syndrome characterised by the presence of prominent anxiety symptoms 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 mediated response to a severe medical condition (e.g., anxiety symptoms or panic attacks in r Also known as: Secondary anxiety syndrome | anxiety disorder due to a general medical condition | medical condition causing anxiety disorder | Organic anxiety disorder | Anxiety syndrome due to health condition not classified under mental and behavioural disorders Excludes: Adjustment disorder | Delirium [6B23.Z] Hypochondriasis, unspecified Also known as: Hypochondriasis, unspecified | Hypochondriasis | Hypochondriacal neurosis | hypochondria | hypochondriacal disorder [6B04] Social anxiety disorder Definition: Social anxiety disorder is characterised by marked and excessive fear or anxiety that consistently occurs in one or more social situations such as social interactions (e.g. having a conversation), doing something while feeling observed (e.g. eating or drinking in the presence of others), or performing in front of others (e.g. giving a speech). The individual is concerned that he or she will act in a way, or show anxiety symptoms, that will be negatively evaluated by others. Relevant social situa Also known as: Social anxiety disorder | social phobia | Social neurosis | Anthropophobia | fear of strangers [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 [JA65.2] Excessive weight gain in pregnancy Definition: Any reason for encounter to assess (or care for) a mother for excessive weight gain during pregnancy. Also known as: Excessive weight gain in pregnancy | excessive weight gain in pregnancy, unspecified trimester | maternal obesity syndrome | maternal obesity without hypertension | abnormal weight gain in pregnancy Excludes: Gestational oedema without hypertension === GRAPH WALKS === --- Walk 1 --- [MB24.3] Anxiety Def: Apprehensiveness or anticipation of future danger or misfortune accompanied by a feeling of worry, distress, or somatic symptoms of tension. The focus of anticipated danger may be internal or external... --PARENT--> [MB24] Symptoms or signs involving mood or affect Def: Symptoms and signs involving the regulation and expression of emotions or feeling states.... --CHILD--> [MB24.1] Anger Def: An emotional state related to one's psychological interpretation of having been threatened that may range in intensity from mild irritation to intense fury and rage.... --- Walk 2 --- [MB24.3] Anxiety Def: Apprehensiveness or anticipation of future danger or misfortune accompanied by a feeling of worry, distress, or somatic symptoms of tension. The focus of anticipated danger may be internal or external... --PARENT--> [MB24] Symptoms or signs involving mood or affect Def: Symptoms and signs involving the regulation and expression of emotions or feeling states.... --CHILD--> [MB24.2] Anhedonia Def: Inability to experience pleasure from normally pleasurable activities.... --- Walk 3 --- [6B00] Generalised anxiety disorder Def: Generalised anxiety disorder is characterised by marked symptoms of anxiety that persist for at least several months, for more days than not, manifested by either general apprehension (i.e. ‘free-floa... --PARENT--> [?] Anxiety or fear-related disorders Def: Anxiety and fear-related disorders are characterised by excessive fear and anxiety and related behavioural disturbances, with symptoms that are severe enough to result in significant distress or signi... --CHILD--> [6B01] Panic disorder Def: Panic disorder is characterised by recurrent unexpected panic attacks that are not restricted to particular stimuli or situations. Panic attacks are discrete episodes of intense fear or apprehension a... --- Walk 4 --- [6B00] Generalised anxiety disorder Def: Generalised anxiety disorder is characterised by marked symptoms of anxiety that persist for at least several months, for more days than not, manifested by either general apprehension (i.e. ‘free-floa... --PARENT--> [?] Anxiety or fear-related disorders Def: Anxiety and fear-related disorders are characterised by excessive fear and anxiety and related behavioural disturbances, with symptoms that are severe enough to result in significant distress or signi... --RELATED_TO--> [?] Secondary anxiety syndrome Def: A syndrome characterised by the presence of prominent anxiety symptoms judged to be a direct pathophysiological consequence of a health condition not classified under mental and behavioural disorders,... --- Walk 5 --- [6E63] Secondary anxiety syndrome Def: A syndrome characterised by the presence of prominent anxiety symptoms judged to be a direct pathophysiological consequence of a health condition not classified under mental and behavioural disorders,... --PARENT--> [?] Secondary mental or behavioural syndromes associated with disorders or diseases classified elsewhere Def: This grouping includes syndromes characterised by the presence of prominent psychological or behavioural symptoms judged to be direct pathophysiological consequences of a medical condition not classif... --EXCLUDES--> [?] 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 6 --- [6E63] Secondary anxiety syndrome Def: A syndrome characterised by the presence of prominent anxiety symptoms judged to be a direct pathophysiological consequence of a health condition not classified under mental and behavioural disorders,... --EXCLUDES--> [?] Adjustment disorder Def: Adjustment disorder is a maladaptive reaction to an identifiable psychosocial stressor or multiple stressors (e.g. divorce, illness or disability, socio-economic problems, conflicts at home or work) t... --EXCLUDES--> [?] Separation anxiety disorder Def: Separation anxiety disorder is characterised by marked and excessive fear or anxiety about separation from specific attachment figures. In children and adolescents, separation anxiety typically focuse...
[ "[MB24.3] Anxiety\n Def: Apprehensiveness or anticipation of future danger or misfortune accompanied by a feeling of worry, distress, or somatic symptoms of tension. The focus of anticipated danger may be internal or external...\n --PARENT--> [MB24] Symptoms or signs involving mood or affect\n Def: Symptoms and signs involving the regulation and expression of emotions or feeling states....\n --CHILD--> [MB24.1] Anger\n Def: An emotional state related to one's psychological interpretation of having been threatened that may range in intensity from mild irritation to intense fury and rage....", "[MB24.3] Anxiety\n Def: Apprehensiveness or anticipation of future danger or misfortune accompanied by a feeling of worry, distress, or somatic symptoms of tension. The focus of anticipated danger may be internal or external...\n --PARENT--> [MB24] Symptoms or signs involving mood or affect\n Def: Symptoms and signs involving the regulation and expression of emotions or feeling states....\n --CHILD--> [MB24.2] Anhedonia\n Def: Inability to experience pleasure from normally pleasurable activities....", "[6B00] Generalised anxiety disorder\n Def: Generalised anxiety disorder is characterised by marked symptoms of anxiety that persist for at least several months, for more days than not, manifested by either general apprehension (i.e. ‘free-floa...\n --PARENT--> [?] Anxiety or fear-related disorders\n Def: Anxiety and fear-related disorders are characterised by excessive fear and anxiety and related behavioural disturbances, with symptoms that are severe enough to result in significant distress or signi...\n --CHILD--> [6B01] Panic disorder\n Def: Panic disorder is characterised by recurrent unexpected panic attacks that are not restricted to particular stimuli or situations. Panic attacks are discrete episodes of intense fear or apprehension a...", "[6B00] Generalised anxiety disorder\n Def: Generalised anxiety disorder is characterised by marked symptoms of anxiety that persist for at least several months, for more days than not, manifested by either general apprehension (i.e. ‘free-floa...\n --PARENT--> [?] Anxiety or fear-related disorders\n Def: Anxiety and fear-related disorders are characterised by excessive fear and anxiety and related behavioural disturbances, with symptoms that are severe enough to result in significant distress or signi...\n --RELATED_TO--> [?] Secondary anxiety syndrome\n Def: A syndrome characterised by the presence of prominent anxiety symptoms judged to be a direct pathophysiological consequence of a health condition not classified under mental and behavioural disorders,...", "[6E63] Secondary anxiety syndrome\n Def: A syndrome characterised by the presence of prominent anxiety symptoms judged to be a direct pathophysiological consequence of a health condition not classified under mental and behavioural disorders,...\n --PARENT--> [?] Secondary mental or behavioural syndromes associated with disorders or diseases classified elsewhere\n Def: This grouping includes syndromes characterised by the presence of prominent psychological or behavioural symptoms judged to be direct pathophysiological consequences of a medical condition not classif...\n --EXCLUDES--> [?] 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...", "[6E63] Secondary anxiety syndrome\n Def: A syndrome characterised by the presence of prominent anxiety symptoms judged to be a direct pathophysiological consequence of a health condition not classified under mental and behavioural disorders,...\n --EXCLUDES--> [?] Adjustment disorder\n Def: Adjustment disorder is a maladaptive reaction to an identifiable psychosocial stressor or multiple stressors (e.g. divorce, illness or disability, socio-economic problems, conflicts at home or work) t...\n --EXCLUDES--> [?] Separation anxiety disorder\n Def: Separation anxiety disorder is characterised by marked and excessive fear or anxiety about separation from specific attachment figures. In children and adolescents, separation anxiety typically focuse..." ]
MB24.3
Anxiety
[ { "from_icd11": "MB24.3", "icd10_code": "R450", "icd10_title": "Nervousness" }, { "from_icd11": "6B00", "icd10_code": "F411", "icd10_title": "Generalized anxiety disorder" }, { "from_icd11": "6E63", "icd10_code": "F064", "icd10_title": "Anxiety disorder due to known physiological condition" }, { "from_icd11": "6B23.Z", "icd10_code": "F4522", "icd10_title": "Body dysmorphic disorder" }, { "from_icd11": "6B23.Z", "icd10_code": "F4521", "icd10_title": "Hypochondriasis" }, { "from_icd11": "6B23.Z", "icd10_code": "F452", "icd10_title": "Hypochondriacal disorders" }, { "from_icd11": "6B04", "icd10_code": "F4010", "icd10_title": "Social phobia, unspecified" }, { "from_icd11": "6B04", "icd10_code": "F4011", "icd10_title": "Social phobia, generalized" }, { "from_icd11": "6B04", "icd10_code": "F401", "icd10_title": "Social phobias" }, { "from_icd11": "MG43.5", "icd10_code": "R634", "icd10_title": "Abnormal weight loss" }, { "from_icd11": "MG43.6", "icd10_code": "R635", "icd10_title": "Abnormal weight gain" }, { "from_icd11": "5B80.0Z", "icd10_code": "E669", "icd10_title": "Obesity, unspecified" }, { "from_icd11": "JA65.2", "icd10_code": "O2603", "icd10_title": "Excessive weight gain in pregnancy, third trimester" }, { "from_icd11": "JA65.2", "icd10_code": "O2601", "icd10_title": "Excessive weight gain in pregnancy, first trimester" }, { "from_icd11": "JA65.2", "icd10_code": "O2602", "icd10_title": "Excessive weight gain in pregnancy, second trimester" } ]
R450
Nervousness
A 36-year-old man was admitted to the emergency department of our level I trauma center after he was run over by a car at approximately 40 km per hour. On arrival, his level of consciousness was fluctuating, and his vital signs were unstable. He was complaining of chest pain and difficulty breathing and had a respiratory rate of 32 breaths per minute with an oxygen saturation of 88%. Physical examination revealed a lip laceration, a road rash covering 40% of his anterior abdominal surface, a large hematoma on the right flank, and pelvic tenderness. Portable radiographs of the chest and pelvis revealed multiple bilateral displaced rib fractures, a left clavicular fracture, small bilateral pneumothoraces, subcutaneous emphysema, and left lung patchy opacities concerning for pulmonary contusions, as well as multiple pelvic fractures with a left sacroiliac joint diastasis. Bilateral chest tubes were placed, and the patient was intubated. The focused assessment with sonography in trauma (FAST) was positive for intra-abdominal free fluid. The patient was taken to the operating room for an emergency exploratory laparotomy. He was found to have a large retroperitoneal zone 3 hematoma and a grade 3 splenic injury. A splenectomy and preperitoneal packing were performed. He also underwent angioembolization of bilateral internal iliac arteries. Post-operatively, he was transferred to the intensive care unit.
3.632813
0.983887
sec[1]/p[1]
en
0.999998
37522945
https://doi.org/10.1007/s00256-023-04415-3
[ "chest", "emergency", "trauma", "abdominal", "large", "hematoma", "pelvic", "multiple", "fractures", "department" ]
[ { "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": "JB22.1", "title": "Delivery by emergency caesarean section" }, { "code": "RA09", "title": "International emergency code 10" }, { "code": "BA03", "title": "Hypertensive crisis" }, { "code": "RA00", "title": "Conditions of uncertain aetiology and emergency use" }, { "code": "RA04", "title": "International emergency code 05" } ]
=== 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 [JB22.1] Delivery by emergency caesarean section Also known as: Delivery by emergency caesarean section | emergency caesarean [RA09] International emergency code 10 Also known as: International emergency code 10 [BA03] Hypertensive crisis Also known as: Hypertensive crisis | Hypertensive emergency | hypertensive crisis with acute organ damage | severely elevated blood pressure with acute organ damage | Hypertensive urgency [RA00] Conditions of uncertain aetiology and emergency use Also known as: Conditions of uncertain aetiology and emergency use [RA04] International emergency code 05 Also known as: International emergency code 05 === 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 --EXCLUDES--> [?] Endocrine, nutritional or metabolic diseases Def: This chapter includes endocrine diseases, nutritional diseases as well as metabolic diseases.... --- 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.... --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 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--> [?] Bronchopleural tuberculosis --- 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... --EXCLUDES--> [?] Primary respiratory tuberculosis without mention of bacteriological or histological confirmation Def: This is a common, and in many cases lethal, infectious disease of the respiratory caused by various strains of mycobacteria, usually Mycobacterium tuberculosis. This diagnosis is without mention of ba...
[ "[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 --EXCLUDES--> [?] Endocrine, nutritional or metabolic diseases\n Def: This chapter includes endocrine diseases, nutritional diseases as well as metabolic diseases....", "[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 --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...", "[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--> [?] Bronchopleural tuberculosis", "[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 --EXCLUDES--> [?] Primary respiratory tuberculosis without mention of bacteriological or histological confirmation\n Def: This is a common, and in many cases lethal, infectious disease of the respiratory caused by various strains of mycobacteria, usually Mycobacterium tuberculosis. This diagnosis is without mention of ba..." ]
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 brachiocephalic trunk was unable to mobilize because it was intimately fused with the anterior wall of the false aneurysm. Therefore, the right subclavian artery was controlled. A temporary bypass (TB) shunt of 20 mm between the ascending and descending aorta was created. In addition, from this bypass an anastomosis with a bifurcation prosthesis for temporary blood supply to the brachiocephalic trunk and left common carotid artery was formed. The first branch of the bifurcated bypass was anastomosed to the right subclavian artery, and the second connected through cannulation to the left carotid artery. The bloodstream was allowed to run through all temporary shunts. The ascending aorta was clamped distal to the shunt, and the descending aorta was clamped proximal to the shunts. Single clamps were placed on the brachiocephalic trunk, left carotid, and left subclavian arteries. Then, a longitudinal aortotomy was made on the front wall of the aortic arch. On the back, the aortic wall was detected, with the defect (with smooth edges, 35 × 20 mm) leading into the cavity of the giant pseudoaneurysm, which was partially filled with old thrombotic material. The posterior aortic wall defect was closed with a Dacron patch. The anterior aortic wall was restored by closing the incision in the aortic wall, with Teflon felt reinforcement. Blood flow was sequentially restored in the aorta and its branches .
4.070313
0.90332
sec[1]/p[7]
en
0.999995
30795033
https://doi.org/10.1055/s-0039-1678553
[ "wall", "aortic", "artery", "aorta", "brachiocephalic", "trunk", "subclavian", "temporary", "bypass", "carotid" ]
[ { "code": "LB0Y", "title": "Other specified structural developmental anomalies of the diaphragm, abdominal wall or umbilical cord" }, { "code": "PA82", "title": "Unintentional striking against stationary object" }, { "code": "NB50.Y&XA3KX0&XJ1C6", "title": "Haematoma of abdominal wall" }, { "code": "DC51.1", "title": "Peritoneal adhesions" }, { "code": "LB73.1Z", "title": "Structural developmental anomalies of chest wall, unspecified" }, { "code": "BD5Z", "title": "Diseases of arteries or arterioles, unspecified" }, { "code": "LA8A.3", "title": "Congenital supravalvar aortic stenosis" }, { "code": "BD40.1", "title": "Atherosclerosis of aorta" }, { "code": "BB71.Z", "title": "Aortic valve insufficiency, unspecified" }, { "code": "LA8B.2Y", "title": "Other specified congenital anomaly of aorta or its branches" } ]
=== ICD-11 CODES FOUND === [LB0Y] Other specified structural developmental anomalies of the diaphragm, abdominal wall or umbilical cord Also known as: Other specified structural developmental anomalies of the diaphragm, abdominal wall or umbilical cord | Congenital deformity of abdominal wall | abdominal wall defect NOS [PA82] Unintentional striking against stationary object Also known as: Unintentional striking against stationary object | striking against stationary object | striking against or struck by other objects | Walked into wall [DC51.1] Peritoneal adhesions Definition: Disorders of peritoneum sticking by scar tissue or fibrosis Also known as: Peritoneal adhesions | abdominal adhesion | adhesive peritoneal band | peritoneal adhesion | peritoneal band Excludes: Adhesions of large intestine with obstruction | Postprocedural pelvic peritoneal adhesions | Intestinal adhesions or bands of small intestine with obstruction [LB73.1Z] Structural developmental anomalies of chest wall, unspecified Also known as: Structural developmental anomalies of chest wall, unspecified | Structural developmental anomalies of chest wall | Malformations of chest wall [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 [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 [BD40.1] Atherosclerosis of aorta Also known as: Atherosclerosis of aorta | aorta atheroma | aorta calcification | aorta arteriosclerosis | aortic degeneration [BB71.Z] Aortic valve insufficiency, unspecified Also known as: Aortic valve insufficiency, unspecified | Aortic valve insufficiency | aortic insufficiency | aortic valve incompetency | AI - [aortic incompetence] [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 === GRAPH WALKS === --- Walk 1 --- [LB0Y] Other specified structural developmental anomalies of the diaphragm, abdominal wall or umbilical cord --PARENT--> [?] Structural developmental anomalies of the diaphragm, abdominal wall or umbilical cord Def: Any condition caused by failure of the diaphragm, abdominal wall or umbilical cord to correctly develop during the antenatal period.... --CHILD--> [LB01] Omphalocele Def: Omphalocele is an embryopathy classified in the group of abdominal celosomias and is characterised by a large hernia of the abdominal wall, centred on the umbilical cord, in which the protruding visce... --- Walk 2 --- [LB0Y] Other specified structural developmental anomalies of the diaphragm, abdominal wall or umbilical cord --PARENT--> [?] Structural developmental anomalies of the diaphragm, abdominal wall or umbilical cord Def: Any condition caused by failure of the diaphragm, abdominal wall or umbilical cord to correctly develop during the antenatal period.... --CHILD--> [LB01] Omphalocele Def: Omphalocele is an embryopathy classified in the group of abdominal celosomias and is characterised by a large hernia of the abdominal wall, centred on the umbilical cord, in which the protruding visce... --- Walk 3 --- [PA82] Unintentional striking against stationary object --PARENT--> [?] Unintentional exposure to object, not elsewhere classified --EXCLUDES--> [?] Assault by exposure to object not elsewhere classified --- Walk 4 --- [PA82] Unintentional striking against stationary object --PARENT--> [?] Unintentional exposure to object, not elsewhere classified --EXCLUDES--> [?] Unintentional contact with person, animal or plant --- Walk 5 --- [DC51.1] Peritoneal adhesions Def: Disorders of peritoneum sticking by scar tissue or fibrosis... --EXCLUDES--> [?] Adhesions of large intestine with obstruction Def: Large bowel obstruction resulting from intraabdominal adhesion due to laparotomy, trauma, and intraabdominal inflammation such as endometriosis.... --CHILD--> [?] Postoperative obstruction of the large intestine --- Walk 6 --- [DC51.1] Peritoneal adhesions Def: Disorders of peritoneum sticking by scar tissue or fibrosis... --EXCLUDES--> [?] Postprocedural pelvic peritoneal adhesions Def: A condition caused by or subsequent to any pelvic intervention leading to damage and inflammation of the peritoneum. This condition is characterised by fibrous bands of scar tissue and abnormal connec... --EXCLUDES--> [?] Endometriosis Def: A condition of the uterus that is frequently idiopathic. This condition is characterised by ectopic growth and function of endometrial tissue outside the uterine cavity. This condition may be associat...
[ "[LB0Y] Other specified structural developmental anomalies of the diaphragm, abdominal wall or umbilical cord\n --PARENT--> [?] Structural developmental anomalies of the diaphragm, abdominal wall or umbilical cord\n Def: Any condition caused by failure of the diaphragm, abdominal wall or umbilical cord to correctly develop during the antenatal period....\n --CHILD--> [LB01] Omphalocele\n Def: Omphalocele is an embryopathy classified in the group of abdominal celosomias and is characterised by a large hernia of the abdominal wall, centred on the umbilical cord, in which the protruding visce...", "[LB0Y] Other specified structural developmental anomalies of the diaphragm, abdominal wall or umbilical cord\n --PARENT--> [?] Structural developmental anomalies of the diaphragm, abdominal wall or umbilical cord\n Def: Any condition caused by failure of the diaphragm, abdominal wall or umbilical cord to correctly develop during the antenatal period....\n --CHILD--> [LB01] Omphalocele\n Def: Omphalocele is an embryopathy classified in the group of abdominal celosomias and is characterised by a large hernia of the abdominal wall, centred on the umbilical cord, in which the protruding visce...", "[PA82] Unintentional striking against stationary object\n --PARENT--> [?] Unintentional exposure to object, not elsewhere classified\n --EXCLUDES--> [?] Assault by exposure to object not elsewhere classified", "[PA82] Unintentional striking against stationary object\n --PARENT--> [?] Unintentional exposure to object, not elsewhere classified\n --EXCLUDES--> [?] Unintentional contact with person, animal or plant", "[DC51.1] Peritoneal adhesions\n Def: Disorders of peritoneum sticking by scar tissue or fibrosis...\n --EXCLUDES--> [?] Adhesions of large intestine with obstruction\n Def: Large bowel obstruction resulting from intraabdominal adhesion due to laparotomy, trauma, and intraabdominal inflammation such as endometriosis....\n --CHILD--> [?] Postoperative obstruction of the large intestine", "[DC51.1] Peritoneal adhesions\n Def: Disorders of peritoneum sticking by scar tissue or fibrosis...\n --EXCLUDES--> [?] Postprocedural pelvic peritoneal adhesions\n Def: A condition caused by or subsequent to any pelvic intervention leading to damage and inflammation of the peritoneum. This condition is characterised by fibrous bands of scar tissue and abnormal connec...\n --EXCLUDES--> [?] Endometriosis\n Def: A condition of the uterus that is frequently idiopathic. This condition is characterised by ectopic growth and function of endometrial tissue outside the uterine cavity. This condition may be associat..." ]
LB0Y
Other specified structural developmental anomalies of the diaphragm, abdominal wall or umbilical cord
[ { "from_icd11": "PA82", "icd10_code": "W2209XA", "icd10_title": "Striking against other stationary object, initial encounter" }, { "from_icd11": "PA82", "icd10_code": "W2201XA", "icd10_title": "Walked into wall, initial encounter" }, { "from_icd11": "PA82", "icd10_code": "W2211XA", "icd10_title": "Striking against or struck by driver side automobile airbag, initial encounter" }, { "from_icd11": "PA82", "icd10_code": "W228XXS", "icd10_title": "Striking against or struck by other objects, sequela" }, { "from_icd11": "PA82", "icd10_code": "W2203XD", "icd10_title": "Walked into furniture, subsequent encounter" }, { "from_icd11": "PA82", "icd10_code": "W2203XA", "icd10_title": "Walked into furniture, initial encounter" }, { "from_icd11": "PA82", "icd10_code": "W228XXD", "icd10_title": "Striking against or struck by other objects, subsequent encounter" }, { "from_icd11": "PA82", "icd10_code": "W2212XA", "icd10_title": "Striking against or struck by front passenger side automobile airbag, initial encounter" }, { "from_icd11": "PA82", "icd10_code": "W2209XS", "icd10_title": "Striking against other stationary object, sequela" }, { "from_icd11": "PA82", "icd10_code": "W228XXA", "icd10_title": "Striking against or struck by other objects, initial encounter" }, { "from_icd11": "PA82", "icd10_code": "W22", "icd10_title": "Striking against or struck by other objects" }, { "from_icd11": "DC51.1", "icd10_code": "K660", "icd10_title": "Peritoneal adhesions (postprocedural) (postinfection)" }, { "from_icd11": "LB73.1Z", "icd10_code": "Q766", "icd10_title": "Other congenital malformations of ribs" }, { "from_icd11": "BD5Z", "icd10_code": "I7389", "icd10_title": "Other specified peripheral vascular diseases" }, { "from_icd11": "BD5Z", "icd10_code": "I7419", "icd10_title": "Embolism and thrombosis of other parts of aorta" } ]
W2209XA
Striking against other stationary object, initial encounter
Our patient had respiratory distress on admission, and nasoendoscopy revealed mild arytenoid and supraglottic swelling. Respiratory condition worsened on day 2 of admission; the patient became progressively more tachypnoeic with increasing secretion load and required supplemental oxygen. Due to work of breathing, she was initially trialled on non-invasive ventilation (NIV) which was soon switched to high-flow nasal cannula (Fi02 0.3, flow rate 30 L/min) in view of inability to clear secretions whilst on NIV. Twenty-four hours later, at the end of day 3 of admission, she developed sudden onset severe respiratory distress with desaturation and required intubation and mechanical ventilation. Clinical examination demonstrated extensive subcutaneous emphysema. Chest X-ray confirmed presence of right-sided pneumothorax, small left-sided pneumothorax, and pneumomediastinum . A chest tube was inserted for the right-sided pneumothorax. Pneumomediastinum and contralateral pneumothorax remained stable on several follow-up images throughout the hospital stay, including CT scan for characterisation . Upper gastrointestinal endoscopy excluded mucosal tear in the pharynx or oesophagus. She was successfully extubated on day 7, and chest tube was removed on day 9. Fig. 6 Chest radiograph showing subcutaneous emphysema, pneumothoraces, and pneumomediastinum (left); CT thorax demonstrating pneumomediastinum (right)
3.689453
0.983398
sec[1]/sec[1]/p[0]
en
0.999997
31205959
https://doi.org/10.1186/s41038-019-0153-4
[ "chest", "pneumothorax", "pneumomediastinum", "respiratory", "sided", "distress", "required", "ventilation", "flow", "subcutaneous" ]
[ { "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": "CB21.Z", "title": "Pneumothorax, unspecified" }, { "code": "CB21.Y", "title": "Other specified pneumothorax" }, { "code": "KB27.1", "title": "Pneumothorax originating in the perinatal period" }, { "code": "NB32.0", "title": "Traumatic pneumothorax" }, { "code": "CB21.0", "title": "Spontaneous tension pneumothorax" } ]
=== 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 [CB21.Z] Pneumothorax, unspecified Also known as: Pneumothorax, unspecified | Pneumothorax | pneumothorax NOS | air leak NOS | pleural air leak NOS [CB21.Y] Other specified pneumothorax Also known as: Other specified pneumothorax | Chronic pneumothorax | Acute pneumothorax | Persistent pneumothorax | Catamenial pneumothorax [KB27.1] Pneumothorax originating in the perinatal period Definition: Abnormal presence of air or other gas in the pleural cavity, usually secondary to tracking of free air from pulmonary interstitial emphysema, or rupture of subpleural blebs. Also known as: Pneumothorax originating in the perinatal period | perinatal pneumothorax | newborn pneumothorax | pneumothorax, perinatal period | congenital pneumothorax [NB32.0] Traumatic pneumothorax Also known as: Traumatic pneumothorax | injury of lung with pneumothorax | chronic traumatic pneumothorax | Postsurgical pneumothorax | pneumothorax, due to operative injury of chest wall or lung [CB21.0] Spontaneous tension pneumothorax Definition: A tension pneumothorax is present when the intrapleural pressure is greater than atmospheric throughout expiration and often during inspiration as well. The mechanism responsible for tension pneumothorax is the disruption of the visceral or parietal pleura in such a manner that a one-way valve develops. A tension pneumothorax can occur after any type of pneumothorax; it is independent of the etiology. It can sometimes occur after a spontaneous pneumothorax but is more common after a traumatic pn Also known as: Spontaneous tension pneumothorax | tension pneumothorax === GRAPH WALKS === --- Walk 1 --- [CB7Z] Diseases of the respiratory system, unspecified --PARENT--> [12] Diseases of the respiratory system --EXCLUDES--> [?] 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 --- [CB7Z] Diseases of the respiratory system, unspecified --PARENT--> [12] Diseases of the respiratory system --PARENT--> [?] ICD-11 for Mortality and Morbidity Statistics --- 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, not confirmed Def: A disease of the respiratory tract, caused by an infection with the bacteria Mycobacterium tuberculosis, which has not been confirmed. This disease is characterised by a chronic cough, and sputum prod... --- Walk 4 --- [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 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... --EXCLUDES--> [?] Primary respiratory tuberculosis without mention of bacteriological or histological confirmation Def: This is a common, and in many cases lethal, infectious disease of the respiratory caused by various strains of mycobacteria, usually Mycobacterium tuberculosis. This diagnosis is without mention of ba... --- 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 --EXCLUDES--> [?] 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...", "[CB7Z] Diseases of the respiratory system, unspecified\n --PARENT--> [12] Diseases of the respiratory system\n --PARENT--> [?] ICD-11 for Mortality and Morbidity Statistics", "[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, not confirmed\n Def: A disease of the respiratory tract, caused by an infection with the bacteria Mycobacterium tuberculosis, which has not been confirmed. This disease is characterised by a chronic cough, and sputum prod...", "[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...", "[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 --EXCLUDES--> [?] Primary respiratory tuberculosis without mention of bacteriological or histological confirmation\n Def: This is a common, and in many cases lethal, infectious disease of the respiratory caused by various strains of mycobacteria, usually Mycobacterium tuberculosis. This diagnosis is without mention of ba...", "[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
A 65-year-old male, a former smoker, with hypertension, type two diabetes mellitus, and dyslipidemia presented with symptoms of angina. Cardiac catheterization revealed triple vessel vessel coronary artery disease and he was scheduled to undergo CABG. After the surgery, the patient was transferred to the ICU for postoperative management. On postoperative day (POD) four, the patient experienced nausea and abdominal pain. Physical exam was remarkable for distended abdomen, hypoactive bowel sounds, and tympanitic sound to percussion. Despite the abdominal complaint, the patient was alert, oriented, and hemodynamically stable. He tolerated a liquid diet and passed flatus, but there were no bowel movements. Abdominal ultrasound was negative for intra-abdominal pathology, and blood tests did not reveal any abnormal electrolyte imbalance. Abdominal X-ray revealed dilation of the central small bowel as well as the colon . Subsequent abdominal CT showed distention of the colon with the cecum and transverse colon measuring 9 cm and 11 cm respectively without any evidence of an obstruction, findings consistent with Ogilvie’s syndrome. The patient was initially managed with bowel rest, nasogastric tube for intermittent suction, and rectal tube without any improvement. Due to the persistence of symptoms, he underwent colonoscopic decompression on POD day nine, which led to the complete resolution of symptoms.
3.695313
0.985352
sec[1]/p[0]
en
0.999998
PMC10545265
https://doi.org/10.7759/cureus.46372
[ "abdominal", "bowel", "colon", "vessel", "postoperative", "without", "tube", "former", "smoker", "hypertension" ]
[ { "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": "DB30.Z", "title": "Obstruction of large intestine, unspecified" }, { "code": "DA96.04", "title": "Short bowel syndrome" }, { "code": "DD3Z", "title": "Ischaemic vascular disorders of intestine, unspecified" }, { "code": "DD30.Z", "title": "Acute vascular disorders of intestine, unspecified" }, { "code": "DA93.0", "title": "Paralytic ileus" } ]
=== 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 [DB30.Z] Obstruction of large intestine, unspecified Also known as: Obstruction of large intestine, unspecified | Obstruction of large intestine | bowel obstruction | large bowel obstruction | abdominal colon obstruction [DA96.04] Short bowel syndrome Definition: Having less than 200 cm of residual small bowel with or without colon in an adult and for children (< 18 yrs), less than 25% of the normal length of intestine for their respective age. Also known as: Short bowel syndrome | Secondary short bowel syndrome | short gut syndrome | short bowel NOS | SBS - [short bowel syndrome] Excludes: Congenital short bowel [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 [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 [DA93.0] Paralytic ileus Definition: A type of ileus, a functional not mechanical obstruction of the small intestines, and a state of pathophysiologic inhibition of motor activity due to non-mechanical causes. The paralysis does not need to be complete, but the intestinal muscles must be so inactive that it leads to a functional blockage of the intestine. Also known as: Paralytic ileus | adynamic ileus | Paralytic ileus of bowel | ileus NOS | paralysis of bowel Excludes: Obstructive ileus of small intestine due to impaction | Gallstone ileus of small intestine === 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.... --CHILD--> [MD81.0] Abdominal tenderness --- 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--> [?] Renal colic Def: A severe paroxysmal pain in the flank radiating to the groin, scrotum or labia, caused by blockage of the renal pelvis or ureter most commonly by a renal stone. May be associated with nausea and vomit... --- 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.... --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 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.Z] Ascites, unspecified --- 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 --CHILD--> [MD81.0] Abdominal tenderness", "[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--> [?] Renal colic\n Def: A severe paroxysmal pain in the flank radiating to the groin, scrotum or labia, caused by blockage of the renal pelvis or ureter most commonly by a renal stone. May be associated with nausea and vomit...", "[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 --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....", "[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", "[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": "DB30.Z", "icd10_code": "K5660", "icd10_title": "Unspecified intestinal obstruction" }, { "from_icd11": "DB30.Z", "icd10_code": "K56600", "icd10_title": "Partial intestinal obstruction, unspecified as to cause" }, { "from_icd11": "DB30.Z", "icd10_code": "K5669", "icd10_title": "Other intestinal obstruction" }, { "from_icd11": "DB30.Z", "icd10_code": "K56609", "icd10_title": "Unspecified intestinal obstruction, unspecified as to partial versus complete obstruction" }, { "from_icd11": "DB30.Z", "icd10_code": "K56699", "icd10_title": "Other intestinal obstruction unspecified as to partial versus complete obstruction" }, { "from_icd11": "DB30.Z", "icd10_code": "K56690", "icd10_title": "Other partial intestinal obstruction" }, { "from_icd11": "DB30.Z", "icd10_code": "K56691", "icd10_title": "Other complete intestinal obstruction" }, { "from_icd11": "DB30.Z", "icd10_code": "K56601", "icd10_title": "Complete intestinal obstruction, unspecified as to cause" }, { "from_icd11": "DB30.Z", "icd10_code": "K567", "icd10_title": "Ileus, unspecified" }, { "from_icd11": "DB30.Z", "icd10_code": "K624", "icd10_title": "Stenosis of anus and rectum" } ]
R100
Acute abdomen
The patient was an 81-year-old woman with left ventricular dysfunction (left ventricular ejection fraction, 49%) and severe chronic kidney disease (Estimated glomerular filtration rate, 10.6 mL/min/1.73m 2 ). She was on warfarin due to long-standing atrial fibrillation (AF). She underwent total arch replacement for Stanford type A acute aortic dissection at age of 70 . During the sternotomy, an epicardial left ventricular lead was placed because she was previously diagnosed as dilated cardiomyopathy with left ventricular ejection fraction of 33% and left bundle branch block. She subsequently underwent cardiac resynchronization therapy-defibrillator (CRT-D) implantation using this lead. Thereafter, a pseudoaneurysm developed around the anastomosis of the prosthetic vascular graft on the proximal side and continued to growth over time. Therefore, she underwent ascending aortic replacement at age of 76 . Although hematoma developed around the prosthetic vascular graft on the ascending aorta one year after the second sternotomy, she followed an uneventful course without symptoms for several years . Fig. 1 Enhanced computed tomography. A : 3D imaging from left anterior oblique; ①Aortic arch replacement on the first sternotomy. ②Ascending aorta replacement on the second sternotomy. B : Axial view; ③Periprosthetic vascular graft hematoma ④Lead on epicardium. ⑤Prosthetic vascular graft on ascending aorta
3.90625
0.981445
sec[0]/sec[0]/p[0]
en
0.999997
38287252
https://doi.org/10.1186/s12872-024-03750-0
[ "ventricular", "replacement", "sternotomy", "vascular", "graft", "ascending", "aorta", "ejection", "fraction", "arch" ]
[ { "code": "LA89.Z", "title": "Functionally univentricular heart, unspecified" }, { "code": "BC45", "title": "Cardiomegaly" }, { "code": "BA41.Z", "title": "Acute myocardial infarction, unspecified" }, { "code": "BC46&XA7XU8", "title": "Ventricular thrombosis" }, { "code": "BD1Z&XT5R", "title": "Acute heart failure" }, { "code": "QA21.6Y", "title": "Other specified surveillance of contraceptive device" }, { "code": "QB51.3", "title": "Presence of otological or audiological implants" }, { "code": "QB30.20", "title": "Adjustment or management of cardiac pacemaker" }, { "code": "QB51.7", "title": "Presence of orthopaedic joint implants" }, { "code": "BC01/BB9Z", "title": "Pulmonary prosthetic valve failure requiring replacement" } ]
=== ICD-11 CODES FOUND === [LA89.Z] Functionally univentricular heart, unspecified Also known as: Functionally univentricular heart, unspecified | Functionally univentricular heart | Univentricular cardiopathy | Single ventricle | univentricular heart [BC45] Cardiomegaly Also known as: Cardiomegaly | enlargement of heart | hypertrophic heart | heart hypertrophy | Cardiac hypertrophy Includes: Left ventricular hyperplasia [BA41.Z] Acute myocardial infarction, unspecified Also known as: Acute myocardial infarction, unspecified | Acute myocardial infarction | cardiac attack | heart attack | acute cardiac infarction [QA21.6Y] Other specified surveillance of contraceptive device Also known as: Other specified surveillance of contraceptive device | Issue of repeat prescription for intrauterine contraceptive device | issue of repeat prescription for contraceptive IUD - [intrauterine device] | Removal of intrauterine contraceptive device | removal of contraceptive device [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 [QB30.20] Adjustment or management of cardiac pacemaker Also known as: Adjustment or management of cardiac pacemaker | change of pacemaker | checking of cardiac pacemaker | checking or testing of cardiac pulse generator battery | checking or testing of pulse generator Excludes: Dysfunction or complication of pacemaker, pacemaker lead or implantable cardioverter defibrillator, not elsewhere classified [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 === GRAPH WALKS === --- Walk 1 --- [LA89.Z] Functionally univentricular heart, unspecified --PARENT--> [LA89] Functionally univentricular heart Def: The term “functionally univentricular heart” describes a spectrum of congenital cardiovascular malformations in which the ventricular mass may not readily lend itself to partitioning that commits one ... --CHILD--> [LA89.2] Mitral atresia Def: A congenital cardiovascular malformation with absence of the mitral valvar annulus (connection/junction) or an imperforate mitral valve.... --- Walk 2 --- [LA89.Z] Functionally univentricular heart, unspecified --PARENT--> [LA89] Functionally univentricular heart Def: The term “functionally univentricular heart” describes a spectrum of congenital cardiovascular malformations in which the ventricular mass may not readily lend itself to partitioning that commits one ... --CHILD--> [LA89.2] Mitral atresia Def: A congenital cardiovascular malformation with absence of the mitral valvar annulus (connection/junction) or an imperforate mitral valve.... --- Walk 3 --- [BC45] Cardiomegaly --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... --CHILD--> [BC42] Myocarditis Def: Myocarditis (inflammatory cardiomyopathy) is inflammation of the heart muscle generally in the presence of a dilated cardiomyopathy that results from exposure to either discrete infectious external an... --- Walk 4 --- [BC45] Cardiomegaly --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... --PARENT--> [11] Diseases of the circulatory system Def: This refers to diseases of the organ system that passes nutrients (such as amino acids, electrolytes and lymph), gases, hormones, blood cells, etc. to and from cells in the body to help fight diseases... --- Walk 5 --- [BA41.Z] Acute myocardial infarction, unspecified --PARENT--> [BA41] Acute myocardial infarction Def: The term acute myocardial infarction (MI) should be used when there is evidence of myocardial necrosis in a clinical setting consistent with acute myocardial ischemia. Under these conditions any one o... --CHILD--> [BA41.1] Acute non-ST elevation myocardial infarction --- Walk 6 --- [BA41.Z] Acute myocardial infarction, unspecified --PARENT--> [BA41] Acute myocardial infarction Def: The term acute myocardial infarction (MI) should be used when there is evidence of myocardial necrosis in a clinical setting consistent with acute myocardial ischemia. Under these conditions any one o... --CHILD--> [BA41.Z] Acute myocardial infarction, unspecified
[ "[LA89.Z] Functionally univentricular heart, unspecified\n --PARENT--> [LA89] Functionally univentricular heart\n Def: The term “functionally univentricular heart” describes a spectrum of congenital cardiovascular malformations in which the ventricular mass may not readily lend itself to partitioning that commits one ...\n --CHILD--> [LA89.2] Mitral atresia\n Def: A congenital cardiovascular malformation with absence of the mitral valvar annulus (connection/junction) or an imperforate mitral valve....", "[LA89.Z] Functionally univentricular heart, unspecified\n --PARENT--> [LA89] Functionally univentricular heart\n Def: The term “functionally univentricular heart” describes a spectrum of congenital cardiovascular malformations in which the ventricular mass may not readily lend itself to partitioning that commits one ...\n --CHILD--> [LA89.2] Mitral atresia\n Def: A congenital cardiovascular malformation with absence of the mitral valvar annulus (connection/junction) or an imperforate mitral valve....", "[BC45] Cardiomegaly\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...\n --CHILD--> [BC42] Myocarditis\n Def: Myocarditis (inflammatory cardiomyopathy) is inflammation of the heart muscle generally in the presence of a dilated cardiomyopathy that results from exposure to either discrete infectious external an...", "[BC45] Cardiomegaly\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...\n --PARENT--> [11] Diseases of the circulatory system\n Def: This refers to diseases of the organ system that passes nutrients (such as amino acids, electrolytes and lymph), gases, hormones, blood cells, etc. to and from cells in the body to help fight diseases...", "[BA41.Z] Acute myocardial infarction, unspecified\n --PARENT--> [BA41] Acute myocardial infarction\n Def: The term acute myocardial infarction (MI) should be used when there is evidence of myocardial necrosis in a clinical setting consistent with acute myocardial ischemia. Under these conditions any one o...\n --CHILD--> [BA41.1] Acute non-ST elevation myocardial infarction", "[BA41.Z] Acute myocardial infarction, unspecified\n --PARENT--> [BA41] Acute myocardial infarction\n Def: The term acute myocardial infarction (MI) should be used when there is evidence of myocardial necrosis in a clinical setting consistent with acute myocardial ischemia. Under these conditions any one o...\n --CHILD--> [BA41.Z] Acute myocardial infarction, unspecified" ]
LA89.Z
Functionally univentricular heart, unspecified
[ { "from_icd11": "LA89.Z", "icd10_code": "Q209", "icd10_title": "Congenital malformation of cardiac chambers and connections, unspecified" }, { "from_icd11": "BC45", "icd10_code": "I517", "icd10_title": "Cardiomegaly" }, { "from_icd11": "BA41.Z", "icd10_code": "I21A1", "icd10_title": "Myocardial infarction type 2" }, { "from_icd11": "BA41.Z", "icd10_code": "I21A9", "icd10_title": "Other myocardial infarction type" }, { "from_icd11": "BA41.Z", "icd10_code": "I2109", "icd10_title": "ST elevation (STEMI) myocardial infarction involving other coronary artery of anterior wall" }, { "from_icd11": "BA41.Z", "icd10_code": "I2119", "icd10_title": "ST elevation (STEMI) myocardial infarction involving other coronary artery of inferior wall" }, { "from_icd11": "BA41.Z", "icd10_code": "I2111", "icd10_title": "ST elevation (STEMI) myocardial infarction involving right coronary artery" }, { "from_icd11": "BA41.Z", "icd10_code": "I2102", "icd10_title": "ST elevation (STEMI) myocardial infarction involving left anterior descending coronary artery" }, { "from_icd11": "BA41.Z", "icd10_code": "I2129", "icd10_title": "ST elevation (STEMI) myocardial infarction involving other sites" }, { "from_icd11": "BA41.Z", "icd10_code": "I2121", "icd10_title": "ST elevation (STEMI) myocardial infarction involving left circumflex coronary artery" }, { "from_icd11": "BA41.Z", "icd10_code": "I2101", "icd10_title": "ST elevation (STEMI) myocardial infarction involving left main coronary artery" }, { "from_icd11": "BA41.Z", "icd10_code": "I214", "icd10_title": "Non-ST elevation (NSTEMI) myocardial infarction" }, { "from_icd11": "BA41.Z", "icd10_code": "I213", "icd10_title": "ST elevation (STEMI) myocardial infarction of unspecified site" }, { "from_icd11": "BA41.Z", "icd10_code": "I219", "icd10_title": "Acute myocardial infarction, unspecified" }, { "from_icd11": "BA41.Z", "icd10_code": "I21", "icd10_title": "Acute myocardial infarction" } ]
Q209
Congenital malformation of cardiac chambers and connections, unspecified
E-NECs are mainly located in the middle-to-lower esophageal segments, due to the greater availability of Merkel cells and endocrine cells in the cardiac glands in the middle and lower esophagus, respectively. These malignant cells may be functional; however, most of them are non-functional, particularly the poorly differentiated ones . E-NECs are usually an incidental finding on UGIE, with the visualization of a single lesion. However, the lesion may appear as an ulcerated or fungating mass, with deep infiltration of the esophageal wall . The symptoms vary according to the size, location, secretory activity, and metastasis of the tumor . Dysphagia and weight loss are the most common presenting symptoms, while dysphonia, odynophagia, retrosternal and epigastric pain, dyspnea, and gastrointestinal bleeding are also reported . Similarly, our case was a female, aged 65 years, who had symptoms for three months and presented with dysphagia, retrosternal burning sensation, weight loss, and altered bowel habits. UGIE revealed a circumferential ulcero-proliferative mass with two umbilicated lesions located in the middle and lower esophageal segments. Additionally, the aggressive nature of the NEC, particularly the high-grade tumor, leads to a high proportion of metastasis during patient presentation . Similarly, due to the high-grade tumor, our patient had metastasis in the regional lymph nodes and liver.
4.113281
0.671875
sec[2]/p[1]
en
0.999996
38410310
https://doi.org/10.7759/cureus.53027
[ "middle", "esophageal", "cells", "metastasis", "tumor", "necs", "located", "segments", "functional", "however" ]
[ { "code": "CB40.2", "title": "Pulmonary collapse" }, { "code": "LA8B.21", "title": "Coarctation of aorta" }, { "code": "AB0Z", "title": "Otitis media, unspecified" }, { "code": "AB1Y&XA0G74", "title": "Fistula of middle ear" }, { "code": "2F91.Y&XA0G74", "title": "Neoplasms of unknown behaviour of middle ear" }, { "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" } ]
=== ICD-11 CODES FOUND === [CB40.2] Pulmonary collapse Also known as: Pulmonary collapse | Atelectasis | lung collapse | pulmonary atelectasis | pulmonary collapse with atelectasis Includes: Atelectasis Excludes: Primary atelectasis of newborn | tuberculous atelectasis, not confirmed | tuberculous atelectasis, confirmed [LA8B.21] Coarctation of aorta Definition: A congenital cardiovascular malformation in which there is a discrete luminal narrowing of the junction between the aortic arch and the descending aorta. Additional information: 'Coarctation of the aorta' generally indicates a narrowing of the descending thoracic aorta just distal to the left subclavian artery. However, the term may also be accurately used to refer to a region of narrowing anywhere in the thoracic or abdominal aorta. Also known as: Coarctation of aorta | aortic coarctation | Preductal coarctation of aorta | Postductal coarctation of aorta | Descending thoracic or abdominal aortic coarctation [AB0Z] Otitis media, unspecified Also known as: Otitis media, unspecified | ear infection | middle ear infection | inflammation of the middle ear | middle ear catarrh [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 === GRAPH WALKS === --- Walk 1 --- [CB40.2] Pulmonary collapse --EXCLUDES--> [?] 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,... --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 2 --- [CB40.2] Pulmonary collapse --EXCLUDES--> [?] Respiratory tuberculosis, not confirmed Def: A disease of the respiratory tract, caused by an infection with the bacteria Mycobacterium tuberculosis, which has not been confirmed. This disease is characterised by a chronic cough, and sputum prod... --CHILD--> [?] Tuberculous pleurisy, not confirmed --- Walk 3 --- [LA8B.21] Coarctation of aorta Def: A congenital cardiovascular malformation in which there is a discrete luminal narrowing of the junction between the aortic arch and the descending aorta. Additional information: 'Coarctation of the a... --PARENT--> [LA8B.2] Congenital anomaly of aorta or its branches Def: A congenital cardiovascular malformation of the aorta and/or its branches.... --CHILD--> [LA8B.22] Interrupted aortic arch Def: A congenital cardiovascular malformation in which there is an absence of luminal continuity between the ascending and descending aorta. Additional information: this includes luminal atresia with disc... --- Walk 4 --- [LA8B.21] Coarctation of aorta Def: A congenital cardiovascular malformation in which there is a discrete luminal narrowing of the junction between the aortic arch and the descending aorta. Additional information: 'Coarctation of the a... --PARENT--> [LA8B.2] Congenital anomaly of aorta or its branches Def: A congenital cardiovascular malformation of the aorta and/or its branches.... --CHILD--> [LA8B.23] Congenital anomaly of descending thoracic or abdominal aorta Def: A congenital cardiovascular malformation of the aorta distal to the aortic arch... --- Walk 5 --- [AB0Z] Otitis media, unspecified --PARENT--> [?] Otitis media --CHILD--> [AB00] Acute otitis media --- Walk 6 --- [AB0Z] Otitis media, unspecified --PARENT--> [?] Otitis media --CHILD--> [?] Suppurative otitis media Def: This involves a perforation (hole) in the tympanic membrane and active bacterial infection within the middle ear space for several weeks or more. There may be enough pus that it drains to the outside ...
[ "[CB40.2] Pulmonary collapse\n --EXCLUDES--> [?] 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,...\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....", "[CB40.2] Pulmonary collapse\n --EXCLUDES--> [?] Respiratory tuberculosis, not confirmed\n Def: A disease of the respiratory tract, caused by an infection with the bacteria Mycobacterium tuberculosis, which has not been confirmed. This disease is characterised by a chronic cough, and sputum prod...\n --CHILD--> [?] Tuberculous pleurisy, not confirmed", "[LA8B.21] Coarctation of aorta\n Def: A congenital cardiovascular malformation in which there is a discrete luminal narrowing of the junction between the aortic arch and the descending aorta.\n\nAdditional information: 'Coarctation of the a...\n --PARENT--> [LA8B.2] Congenital anomaly of aorta or its branches\n Def: A congenital cardiovascular malformation of the aorta and/or its branches....\n --CHILD--> [LA8B.22] Interrupted aortic arch\n Def: A congenital cardiovascular malformation in which there is an absence of luminal continuity between the ascending and descending aorta.\n\nAdditional information: this includes luminal atresia with disc...", "[LA8B.21] Coarctation of aorta\n Def: A congenital cardiovascular malformation in which there is a discrete luminal narrowing of the junction between the aortic arch and the descending aorta.\n\nAdditional information: 'Coarctation of the a...\n --PARENT--> [LA8B.2] Congenital anomaly of aorta or its branches\n Def: A congenital cardiovascular malformation of the aorta and/or its branches....\n --CHILD--> [LA8B.23] Congenital anomaly of descending thoracic or abdominal aorta\n Def: A congenital cardiovascular malformation of the aorta distal to the aortic arch...", "[AB0Z] Otitis media, unspecified\n --PARENT--> [?] Otitis media\n --CHILD--> [AB00] Acute otitis media", "[AB0Z] Otitis media, unspecified\n --PARENT--> [?] Otitis media\n --CHILD--> [?] Suppurative otitis media\n Def: This involves a perforation (hole) in the tympanic membrane and active bacterial infection within the middle ear space for several weeks or more. There may be enough pus that it drains to the outside ..." ]
CB40.2
Pulmonary collapse
[ { "from_icd11": "CB40.2", "icd10_code": "J9811", "icd10_title": "Atelectasis" }, { "from_icd11": "CB40.2", "icd10_code": "J9819", "icd10_title": "Other pulmonary collapse" }, { "from_icd11": "CB40.2", "icd10_code": "J981", "icd10_title": "Pulmonary collapse" }, { "from_icd11": "LA8B.21", "icd10_code": "Q251", "icd10_title": "Coarctation of aorta" }, { "from_icd11": "LA8B.21", "icd10_code": "Q251 ", "icd10_title": "" }, { "from_icd11": "AB0Z", "icd10_code": "H673", "icd10_title": "Otitis media in diseases classified elsewhere, bilateral" }, { "from_icd11": "AB0Z", "icd10_code": "H6690", "icd10_title": "Otitis media, unspecified, unspecified ear" }, { "from_icd11": "AB0Z", "icd10_code": "H6693", "icd10_title": "Otitis media, unspecified, bilateral" }, { "from_icd11": "AB0Z", "icd10_code": "H669", "icd10_title": "Otitis media, unspecified" }, { "from_icd11": "AB0Z", "icd10_code": "H67", "icd10_title": "Otitis media in diseases classified elsewhere" }, { "from_icd11": "AB0Z", "icd10_code": "H670", "icd10_title": "" }, { "from_icd11": "AB0Z", "icd10_code": "H671", "icd10_title": "Otitis media in diseases classified elsewhere, right ear" }, { "from_icd11": "AB0Z", "icd10_code": "H678", "icd10_title": "" }, { "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" } ]
J9811
Atelectasis
Faced with irreversible colon necrosis, resection of sigmoid colon and descending colon and proximal colostomy was performed. The closure of the rectal stump, below the peritoneal reflection, was performed with mechanical suture. As there was no response to induction via vaginal labor and the patient conditions were critical, it was decided to carry out a postmortem cesarean section. However, after removal of the dead fetus, the patient showed a uterine atony by severe bleeding, about 800 mL of blood, and it was refractory to standard clinical measures. Unfortunately, she required a concomitant total abdominal hysterectomy. After cesarean section, the peritoneal cavity was washing with saline and the abdominal wall was closing by planes. As the patient remained shocked and with respiratory distress syndrome during the surgical procedure, and she had received 4 UI of the plasma and 1 UI of the red blood cell concentration, the postoperative was followed at unit of intensive care. She remained for four days on mechanical ventilation and broad-spectrum antibiotic therapy. The renal and respiratory failure was improving gradually being transferred on the 7th day to the infirmary. With progressive improvement in general condition and normalization of pulmonary and renal function, she was discharged on 15th postoperative days. Colostomy was closed after three months and colorectal anastomosis was done.
3.568359
0.983398
sec[1]/p[4]
en
0.999996
22567527
https://doi.org/10.1155/2012/641093
[ "colon", "colostomy", "peritoneal", "mechanical", "cesarean", "section", "blood", "abdominal", "remained", "respiratory" ]
[ { "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": "DE12.0", "title": "Colostomy or enterostomy malfunction or complication" }, { "code": "QB62.3", "title": "Attention to colostomy" }, { "code": "QB61.4", "title": "Presence of colostomy" }, { "code": "DE12.0/ME24.4", "title": "Colostomy stenosis" }, { "code": "DE12.0/ME24.1", "title": "Colostomy fistula" } ]
=== 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 [DE12.0] Colostomy or enterostomy malfunction or complication Also known as: Colostomy or enterostomy malfunction or complication | colostomy and enterostomy complication, unspecified | colostomy and enterostomy complications | malfunction of colostomy and enterostomy | Ileostomy malfunction [QB62.3] Attention to colostomy Also known as: Attention to colostomy | colon stoma care | colostomy care | stoma care of colostomy [QB61.4] Presence of colostomy Also known as: Presence of colostomy | colon stoma status | colostomy status === GRAPH WALKS === --- Walk 1 --- [NB91.81] Laceration of colon Def: A tear or wound of large intestine.... --PARENT--> [NB91.8] Injury of colon --CHILD--> [NB91.82] 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 2 --- [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 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... --EXCLUDES--> [?] Necrotising enterocolitis of newborn Def: This is a fulminating disease of neonates in which there is extensive mucosal ulceration, pseudomembrane formation, submucosal haemorrhage, and necrosis usually of the right colon, caecum, terminal il... --- 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... --CHILD--> [DD3Y] Other specified ischaemic vascular disorders of intestine
[ "[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....", "[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....", "[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 --EXCLUDES--> [?] Necrotising enterocolitis of newborn\n Def: This is a fulminating disease of neonates in which there is extensive mucosal ulceration, pseudomembrane formation, submucosal haemorrhage, and necrosis usually of the right colon, caecum, terminal il...", "[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--> [DD3Y] Other specified ischaemic vascular disorders of intestine" ]
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": "DE12.0", "icd10_code": "K914", "icd10_title": "" }, { "from_icd11": "QB62.3", "icd10_code": "Z433", "icd10_title": "Encounter for attention to colostomy" }, { "from_icd11": "QB61.4", "icd10_code": "Z933", "icd10_title": "Colostomy status" } ]
K559
Vascular disorder of intestine, unspecified
Extensive additional testing was performed for infectious diseases, including serology enzyme-linked immunosorbent assay (ELISA) testing for Dirofilaria immitis , Ehrlichia canis , E. ewengii , Borrelia burgdorferi , Anaplasma phagocytophilum , and A. platys , enzyme immunoassay (EIA) urine antigen testing for Blastomyces dermatitidis , and serology immunofluorescent antibody tests (IFAT) for Ehrlichia canis , Rickettsia rickettsii , Borrelia burgdorferi , Babesia canis , Cryptococcus neoformans , Toxoplasma gondii , and Neospora caninum . Submitted antibody titers returned positive for IgG against Neospora caninum , with an IFAT dilution titer of 1:4096 (the baseline dilution is 1:32). All other antibody titers and antemortem infectious disease testing performed were negative. Due to the rapid progression of clinical signs, treatment was initiated before diagnostic results were received, and the patient was placed on broad spectrum antimicrobials including clindamycin (12.5 mg/kg twice daily) and trimethoprim/sulfamethoxazole (TMS, 20 mg/kg twice daily) as well as dexamethasone SP (0.14 mg/kg once daily) and gabapentin (8.3 mg/kg twice daily) to control inflammation and pain pending definitive diagnostic results. Two days after diagnostic testing was performed, the patient acutely experienced cardiac arrest. The body was submitted to the Purdue Animal Disease Diagnostic Laboratory for necropsy.
4.058594
0.925293
sec[1]/sec[0]/p[2]
en
0.999997
39591318
https://doi.org/10.3390/vetsci11110544
[ "testing", "daily", "canis", "antibody", "twice", "infectious", "including", "serology", "enzyme", "ehrlichia" ]
[ { "code": "QA40", "title": "Pregnancy examination or test" }, { "code": "QA00.6Z", "title": "Examination of eyes or vision, unspecified" }, { "code": "QA00.7", "title": "Examination of ears and hearing" }, { "code": "QA00.A", "title": "Skin or other sensitisation tests" }, { "code": "QA3Y", "title": "Contact with health services for other specified procreative management" }, { "code": "QF21", "title": "Difficulty or need for assistance with general life tasks or life management" }, { "code": "8A83", "title": "Other primary headache disorder" }, { "code": "QB42", "title": "Dependence on renal dialysis" }, { "code": "1F6D", "title": "Toxocariasis" }, { "code": "1B95", "title": "Brucellosis" } ]
=== ICD-11 CODES FOUND === [QA40] Pregnancy examination or test Also known as: Pregnancy examination or test | pregnancy examination | pregnancy test | Pregnancy examination or test, pregnancy not confirmed | pregnancy not yet confirmed [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 [QA00.7] Examination of ears and hearing Also known as: Examination of ears and hearing | examination of ear | hearing examination | hearing test [QA00.A] Skin or other sensitisation tests Also known as: Skin or other sensitisation tests | diagnostic skin or sensitisation tests | general skin examination | Skin tests for bacterial disease | Skin tests for hypersensitivity [QA3Y] Contact with health services for other specified procreative management Also known as: Contact with health services for other specified procreative management | Procreative investigation or testing | procreative test | Fallopian tube insufflation | Sperm count for procreative test [QF21] Difficulty or need for assistance with general life tasks or life management Also known as: Difficulty or need for assistance with general life tasks or life management | difficulty with carrying out tasks and daily routine | life management problem | difficulty with life management tasks | Difficulty with dealing with change such as relocation Includes: difficulty with carrying out tasks and daily routine [8A83] Other primary headache disorder Definition: A group of clinically heterogeneous headache disorders, believed to be primary. Although largely unrelated, they fall into four categories: headaches associated with physical exertion; headaches attributed to direct physical but innocuous stimuli; epicranial headaches; and other miscellaneous primary headache disorders. Also known as: Other primary headache disorder | Primary cough headache | Primary exercise headache | Primary headache associated with sexual activity | Preorgasmic headache [QB42] Dependence on renal dialysis Also known as: Dependence on renal dialysis | renal dialysis status | presence of arteriovenous shunt for dialysis | dependence on haemodialysis | Dependence on renal dialysis, acute haemodialysis Includes: renal dialysis status Excludes: dialysis preparation, treatment or session [1F6D] Toxocariasis Definition: A condition caused by an infection with the parasitic worm Toxocara. In ocular infections, this condition is characterised by vision loss or inflammation of the eye; in visceral infections, this condition is characterised by fever, coughing, enlarged liver, or pneumonia. This condition may also be asymptomatic. Transmission is by the faecal-oral route through the ingestion of food, water, or soil that contains Toxocara eggs (contaminated by faeces from an infected dog or cat). Confirmation is by Also known as: Toxocariasis | Visceral larva migrans | Larva migrans visceralis | toxocaral visceral larva migrans | visceral larva migrans syndrome Includes: Toxocara infestation [1B95] Brucellosis Definition: A disease caused by an infection with the gram-negative bacteria Brucella. This disease is characterised by fever, muscular pain, or sweating. Transmission is by ingestion of unpasteurized milk and soft cheeses made from infected animals. Confirmation is by identification of Brucella or antibodies to Brucella. Also known as: Brucellosis | Malta fever | Mediterranean fever | undulant fever | brucellosis infection Includes: Malta fever | Mediterranean fever | undulant fever === GRAPH WALKS === --- Walk 1 --- [QA40] Pregnancy examination or test --PARENT--> [?] Contact with health services for reasons associated with reproduction --RELATED_TO--> [?] Contact with health services for preimplantation genetic diagnosis Def: A reason for encounter to genetically profile oocytes, zygotes, or embryos through in vitro fertilization prior to implantation for diagnosis of genetic, structural, or chromosomal alterations.... --- Walk 2 --- [QA40] Pregnancy examination or test --PARENT--> [?] Contact with health services for reasons associated with reproduction --CHILD--> [QA21] Contact with health services for contraceptive management --- Walk 3 --- [QA00.6Z] Examination of eyes or vision, unspecified --PARENT--> [QA00.6] Examination of eyes or vision --EXCLUDES--> [?] Examination for driving license --- Walk 4 --- [QA00.6Z] Examination of eyes or vision, unspecified --PARENT--> [QA00.6] Examination of eyes or vision --CHILD--> [QA00.6Y] Other specified examination of eyes or vision --- Walk 5 --- [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 6 --- [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
[ "[QA40] Pregnancy examination or test\n --PARENT--> [?] Contact with health services for reasons associated with reproduction\n --RELATED_TO--> [?] Contact with health services for preimplantation genetic diagnosis\n Def: A reason for encounter to genetically profile oocytes, zygotes, or embryos through in vitro fertilization prior to implantation for diagnosis of genetic, structural, or chromosomal alterations....", "[QA40] Pregnancy examination or test\n --PARENT--> [?] Contact with health services for reasons associated with reproduction\n --CHILD--> [QA21] Contact with health services for contraceptive management", "[QA00.6Z] Examination of eyes or vision, unspecified\n --PARENT--> [QA00.6] Examination of eyes or vision\n --EXCLUDES--> [?] Examination for driving license", "[QA00.6Z] Examination of eyes or vision, unspecified\n --PARENT--> [QA00.6] Examination of eyes or vision\n --CHILD--> [QA00.6Y] Other specified examination of eyes or vision", "[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", "[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" ]
QA40
Pregnancy examination or test
[ { "from_icd11": "QA40", "icd10_code": "Z3201", "icd10_title": "Encounter for pregnancy test, result positive" }, { "from_icd11": "QA40", "icd10_code": "Z3200", "icd10_title": "Encounter for pregnancy test, result unknown" }, { "from_icd11": "QA40", "icd10_code": "Z3202", "icd10_title": "Encounter for pregnancy test, result negative" }, { "from_icd11": "QA40", "icd10_code": "Z32", "icd10_title": "Encounter for pregnancy test and childbirth and childcare instruction" }, { "from_icd11": "QA40", "icd10_code": "Z320", "icd10_title": "Encounter for pregnancy test" }, { "from_icd11": "QA40", "icd10_code": "Z321", "icd10_title": "" }, { "from_icd11": "QA00.6Z", "icd10_code": "Z010", "icd10_title": "Encounter for examination of eyes and vision" }, { "from_icd11": "QA00.7", "icd10_code": "Z011", "icd10_title": "Encounter for examination of ears and hearing" }, { "from_icd11": "QA00.A", "icd10_code": "Z015", "icd10_title": "" }, { "from_icd11": "QF21", "icd10_code": "Z742", "icd10_title": "Need for assistance at home and no other household member able to render care" }, { "from_icd11": "QF21", "icd10_code": "Z600", "icd10_title": "Problems of adjustment to life-cycle transitions" }, { "from_icd11": "8A83", "icd10_code": "G44209", "icd10_title": "Tension-type headache, unspecified, not intractable" }, { "from_icd11": "8A83", "icd10_code": "G44221", "icd10_title": "Chronic tension-type headache, intractable" }, { "from_icd11": "8A83", "icd10_code": "G44229", "icd10_title": "Chronic tension-type headache, not intractable" }, { "from_icd11": "8A83", "icd10_code": "G44201", "icd10_title": "Tension-type headache, unspecified, intractable" } ]
Z3201
Encounter for pregnancy test, result positive
The patient’s baseline ECG 1 month before admission, performed for atrial fibrillation monitoring, demonstrated sinus bradycardia at 55 beats/min and a QRS complex duration of 104 milliseconds . An ECG taken during an episode of WCT showed a regular wide complex monomorphic tachycardia at a rate of 120 beats/min, with a normal axis, a QRS complex duration of 196 milliseconds, a long intrinsicoid, and a left bundle branch block configuration pattern . An ECG obtained between WCT episodes showed sinus bradycardia at 51 beats/min with diffuse large T-wave inversions and with a QRS complex duration of 138 milliseconds and a QTc interval (Bazett) of 627 milliseconds . Laboratory tests revealed normal values of serum electrolytes, thyroid-stimulating hormone, renal function panel, and hemoglobin at baseline. The TTE on admission showed a newly reduced ejection fraction of 30% ± 5%, new periapical akinesis, and ballooning of the left ventricle suggestive of apical takotsubo syndrome . Figure 1 Baseline Electrocardiogram 1 Month Before Hospitalization Figure 2 Electrocardiogram Showing Wide QRS Complex Tachycardia Figure 3 Electrocardiogram Between Wide Complex Tachycardia Episodes Showing Diffuse Large T-Wave Inversions With a Prolonged QT Interval Figure 4 Transthoracic Echocardiogram (Left) Apical 3-chamber view showing diastole) compared with (right) systolic apical ballooning of the left ventricle.
4.121094
0.937012
sec[3]/p[0]
en
0.999997
PMC11775788
https://doi.org/10.1016/j.jaccas.2024.102811
[ "complex", "milliseconds", "baseline", "beats", "duration", "wide", "tachycardia", "apical", "electrocardiogram", "sinus" ]
[ { "code": "LA88.2Z", "title": "Tetralogy of Fallot, unspecified" }, { "code": "5A70.Y", "title": "Other specified Cushing syndrome" }, { "code": "1B10.Z", "title": "Respiratory tuberculosis, without mention of bacteriological or histological confirmation" }, { "code": "6B41", "title": "Complex post traumatic stress disorder" }, { "code": "LA88.Y", "title": "Other specified congenital anomaly of a ventricle or the ventricular septum" }, { "code": "BC60", "title": "Atrial premature depolarization" }, { "code": "BC70", "title": "Ventricular premature depolarization" }, { "code": "MC81.Z", "title": "Abnormalities of heart beat, unspecified" }, { "code": "MC81.0", "title": "Tachycardia, unspecified" }, { "code": "MC81.Y", "title": "Other specified abnormalities of heart beat" } ]
=== ICD-11 CODES FOUND === [LA88.2Z] Tetralogy of Fallot, unspecified Also known as: Tetralogy of Fallot, unspecified | Tetralogy of Fallot | tetrad of Fallot | Fallot tetralogy | Fallot tetrad [5A70.Y] Other specified Cushing syndrome Also known as: Other specified Cushing syndrome | ACTH-dependent Cushing syndrome | ACTH-independent Cushing syndrome | ACTH-independent Cushing syndrome due to bilateral adrenocortical hyperplasia | ACTH-independent macronodular adrenal hyperplasia [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 [6B41] Complex post traumatic stress disorder Definition: Complex post traumatic stress disorder (Complex PTSD) is a disorder that may develop following exposure to an event or series of events of an extremely threatening or horrific nature, most commonly prolonged or repetitive events from which escape is difficult or impossible (e.g. torture, slavery, genocide campaigns, prolonged domestic violence, repeated childhood sexual or physical abuse). All diagnostic requirements for PTSD are met. In addition, Complex PTSD is characterised by severe and pers Also known as: Complex post traumatic stress disorder | enduring personality change after catastrophic experience | complex PTSD | personality change after disasters | Personality change after concentration camp experiences Excludes: Post traumatic stress disorder | Personality disorder [LA88.Y] Other specified congenital anomaly of a ventricle or the ventricular septum Also known as: Other specified congenital anomaly of a ventricle or the ventricular septum | Congenital right ventricular anomaly | Right ventricular hypoplasia | Hypoplastic right ventricle | Right ventricular myocardial sinusoids [BC60] Atrial premature depolarization Definition: Cardiac electrical depolarization arising from the atria, occurring earlier than the expected sinus beat Also known as: Atrial premature depolarization | atrial extrasystoles | ectopic atrial beats | premature atrial contraction | premature atrial beats [BC70] Ventricular premature depolarization Definition: Ventricular depolarization occurring earlier than the expected ventricular depolarization initiated by the sinoatrial node or another supraventricular pacemaker. Also known as: Ventricular premature depolarization | premature ventricular complex | premature ventricular contraction | premature ventricular systole | ventricular ectopic beats [MC81.Z] Abnormalities of heart beat, unspecified Also known as: Abnormalities of heart beat, unspecified | Abnormalities of heart beat | abnormal heart rate | abnormal rhythm disorder | abnormal rhythms [MC81.0] Tachycardia, unspecified Also known as: Tachycardia, unspecified | heart rate fast | rapid heart | Rapid heart beat | increased heart rate [MC81.Y] Other specified abnormalities of heart beat Also known as: Other specified abnormalities of heart beat | Coupled rhythm | Gallop rhythm | Pulse, alternating | Pulse, bigeminal === GRAPH WALKS === --- Walk 1 --- [LA88.2Z] Tetralogy of Fallot, unspecified --PARENT--> [LA88.2] Tetralogy of Fallot Def: A group of congenital cardiovascular malformations with biventricular atrioventricular alignments or connections characterised by anterosuperior deviation of the conal or outlet septum or its fibrous ... --CHILD--> [LA88.21] Tetralogy of Fallot with pulmonary atresia Def: A congenital cardiovascular malformation that is a variant of tetralogy of Fallot in which there is no direct communication between the right ventricle and the pulmonary arterial tree.... --- Walk 2 --- [LA88.2Z] Tetralogy of Fallot, unspecified --PARENT--> [LA88.2] Tetralogy of Fallot Def: A group of congenital cardiovascular malformations with biventricular atrioventricular alignments or connections characterised by anterosuperior deviation of the conal or outlet septum or its fibrous ... --CHILD--> [LA88.20] Tetralogy of Fallot with absent pulmonary valve syndrome Def: A congenital cardiovascular malformation that is a variant of tetralogy of Fallot in which the ventriculo-arterial junction of the right ventricle with the pulmonary trunk features an atypical valve w... --- Walk 3 --- [5A70.Y] Other specified Cushing syndrome --PARENT--> [5A70] Cushing syndrome Def: Cushing syndrome results from excess of corticosteroid hormones in the body due to overstimulation of the adrenal glands by excessive amounts of the hormone ACTH, secreted either by a tumuor of the pi... --CHILD--> [5A70.0] Pituitary-dependent Cushing disease Def: Pituitary-dependent Cushing disease is caused by a pituitary tumour, generally benign (adenoma) but rarely malignant (carcinoma), which secretes adrenocorticotropin (ACTH) autonomously, leading to hyp... --- Walk 4 --- [5A70.Y] Other specified Cushing syndrome --PARENT--> [5A70] Cushing syndrome Def: Cushing syndrome results from excess of corticosteroid hormones in the body due to overstimulation of the adrenal glands by excessive amounts of the hormone ACTH, secreted either by a tumuor of the pi... --PARENT--> [?] Disorders of the adrenal glands or adrenal hormone system --- Walk 5 --- [1B10.Z] Respiratory tuberculosis, without mention of bacteriological or histological confirmation --PARENT--> [1B10] 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.... --PARENT--> [?] Tuberculosis Def: A disease caused by an infection with bacteria of the Mycobacterium tuberculosis complex. This disease presents with symptoms depending on the site of infection. Transmission is commonly by inhalation... --- Walk 6 --- [1B10.Z] Respiratory tuberculosis, without mention of bacteriological or histological confirmation --PARENT--> [1B10] 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--> [1B10.Z] Respiratory tuberculosis, without mention of bacteriological or histological confirmation
[ "[LA88.2Z] Tetralogy of Fallot, unspecified\n --PARENT--> [LA88.2] Tetralogy of Fallot\n Def: A group of congenital cardiovascular malformations with biventricular atrioventricular alignments or connections characterised by anterosuperior deviation of the conal or outlet septum or its fibrous ...\n --CHILD--> [LA88.21] Tetralogy of Fallot with pulmonary atresia\n Def: A congenital cardiovascular malformation that is a variant of tetralogy of Fallot in which there is no direct communication between the right ventricle and the pulmonary arterial tree....", "[LA88.2Z] Tetralogy of Fallot, unspecified\n --PARENT--> [LA88.2] Tetralogy of Fallot\n Def: A group of congenital cardiovascular malformations with biventricular atrioventricular alignments or connections characterised by anterosuperior deviation of the conal or outlet septum or its fibrous ...\n --CHILD--> [LA88.20] Tetralogy of Fallot with absent pulmonary valve syndrome\n Def: A congenital cardiovascular malformation that is a variant of tetralogy of Fallot in which the ventriculo-arterial junction of the right ventricle with the pulmonary trunk features an atypical valve w...", "[5A70.Y] Other specified Cushing syndrome\n --PARENT--> [5A70] Cushing syndrome\n Def: Cushing syndrome results from excess of corticosteroid hormones in the body due to overstimulation of the adrenal glands by excessive amounts of the hormone ACTH, secreted either by a tumuor of the pi...\n --CHILD--> [5A70.0] Pituitary-dependent Cushing disease\n Def: Pituitary-dependent Cushing disease is caused by a pituitary tumour, generally benign (adenoma) but rarely malignant (carcinoma), which secretes adrenocorticotropin (ACTH) autonomously, leading to hyp...", "[5A70.Y] Other specified Cushing syndrome\n --PARENT--> [5A70] Cushing syndrome\n Def: Cushing syndrome results from excess of corticosteroid hormones in the body due to overstimulation of the adrenal glands by excessive amounts of the hormone ACTH, secreted either by a tumuor of the pi...\n --PARENT--> [?] Disorders of the adrenal glands or adrenal hormone system", "[1B10.Z] Respiratory tuberculosis, without mention of bacteriological or histological confirmation\n --PARENT--> [1B10] 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 --PARENT--> [?] Tuberculosis\n Def: A disease caused by an infection with bacteria of the Mycobacterium tuberculosis complex. This disease presents with symptoms depending on the site of infection. Transmission is commonly by inhalation...", "[1B10.Z] Respiratory tuberculosis, without mention of bacteriological or histological confirmation\n --PARENT--> [1B10] 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--> [1B10.Z] Respiratory tuberculosis, without mention of bacteriological or histological confirmation" ]
LA88.2Z
Tetralogy of Fallot, unspecified
[ { "from_icd11": "LA88.2Z", "icd10_code": "Q213", "icd10_title": "Tetralogy of Fallot" }, { "from_icd11": "LA88.2Z", "icd10_code": "Q213 ", "icd10_title": "" }, { "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": "6B41", "icd10_code": "F62", "icd10_title": "" }, { "from_icd11": "6B41", "icd10_code": "F620", "icd10_title": "" }, { "from_icd11": "BC60", "icd10_code": "I491", "icd10_title": "Atrial premature depolarization" }, { "from_icd11": "BC60", "icd10_code": "I49", "icd10_title": "Other cardiac arrhythmias" }, { "from_icd11": "BC70", "icd10_code": "I493", "icd10_title": "Ventricular premature depolarization" }, { "from_icd11": "MC81.Z", "icd10_code": "R009", "icd10_title": "Unspecified abnormalities of heart beat" } ]
Q213
Tetralogy of Fallot
Postoperatively, the patient was admitted to the intensive care unit for the management of heart failure. Oxygen administration was initiated at 30 L/min with a high nasal flow rate, and SpO2 was maintained at 99%. A bolus dose of 10 mg furosemide was administered to treat pulmonary edema. On the first postoperative day, chest radiography revealed a CTAR of 67%, worsening cardiac enlargement, and pulmonary congestion that had not improved. However, SpO2 was maintained at 99% even when the oxygen dosage was reduced to 5 L/min of mask oxygen. At this point, the patient was still poorly oxygenated with an arterial oxygen partial pressure (PaO2) to the fraction of inspired oxygen (FiO2) ratio or P/F ratio of 260; therefore, she continued to be managed in the intensive care unit. On the second postoperative day, oxygen was administered at 3 L/min of mask oxygen. SpO2 was stable at 99%, chest radiography showed a slight improvement with a CTAR of 62%, the pulmonary congestion improved, and the P/F ratio was 318, all of which indicated improved oxygenation. Oxygen administration was gradually tapered off. On the fifth postoperative day, SpO2 was maintained at 99% and oxygen administration was terminated. The NYHA of the patient improved from IV to III. On the seventh postoperative day, propranolol hydrochloride was administered to treat HCM. At the one-month checkup, her NYHA score had improved to II .
3.765625
0.973633
sec[1]/p[5]
en
0.999996
40276453
https://doi.org/10.7759/cureus.81124
[ "oxygen", "improved", "postoperative", "administration", "maintained", "pulmonary", "intensive", "unit", "treat", "chest" ]
[ { "code": "MD11.1", "title": "Asphyxia" }, { "code": "NE60", "title": "Harmful effects of drugs, medicaments or biological substances, not elsewhere classified" }, { "code": "3A51.7", "title": "High affinity haemoglobin" }, { "code": "NF05", "title": "Asphyxiation" }, { "code": "PB08", "title": "Unintentional threat to breathing from low oxygen environment" }, { "code": "NE81.0Z", "title": "Haemorrhage or haematoma of other or unspecified site complicating a procedure, not elsewhere classified" }, { "code": "NE81.3", "title": "Postsurgical leak" }, { "code": "QF00", "title": "Acquired absence of limb" }, { "code": "DB30.2", "title": "Adhesions of large intestine with obstruction" }, { "code": "MG30.21", "title": "Chronic postsurgical pain" } ]
=== ICD-11 CODES FOUND === [MD11.1] Asphyxia Definition: Asphyxia is a life-threatening condition in which oxygen is prevented from reaching the tissues by obstruction of or damage to any part of the respiratory system. More generally the term indicates all the conditions generating impaired or impeded breathing. Also known as: Asphyxia | pathological asphyxia | decreased oxygen supply | oxygen deficiency | positional asphyxia Excludes: asphyxia due to foreign body in respiratory tract | asphyxia due to carbon monoxide | asphyxia due to traumatic [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 [3A51.7] High affinity haemoglobin Definition: A disease caused by determinants arising after birth, in the antenatal period or by genetically inherited factors leading to high oxygen affinity haemoglobin. This disease is characterised by abnormalities in the globin chains that alter the affinity of the haemoglobin molecule for oxygen, affecting the normal loading of oxygen in the lungs and delivery of oxygen to the tissues. Also known as: High affinity haemoglobin | Haemoglobins with abnormal oxygen affinity [NF05] Asphyxiation Also known as: Asphyxiation | suffocation NOS | traumatic asphyxia | positional asphyxiation | asphyxia (ligature) Excludes: Respiratory distress of newborn | Adult acute respiratory distress syndrome | asphyxia from carbon monoxide [PB08] Unintentional threat to breathing from low oxygen environment Also known as: Unintentional threat to breathing from low oxygen environment | confined to or trapped in a low-oxygen environment | Accidental mechanical suffocation in refrigerator | Diving with insufficient air supply | Accidentally shut in other airtight space [NE81.0Z] Haemorrhage or haematoma of other or unspecified site complicating a procedure, not elsewhere classified Also known as: Haemorrhage or haematoma of other or unspecified site complicating a procedure, not elsewhere classified | Haemorrhage or haematoma complicating a procedure, not elsewhere classified | postoperative haemorrhage | postoperative bleeding | Haemorrhage at any site resulting from a procedure [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 [QF00] Acquired absence of limb Also known as: Acquired absence of limb | post traumatic loss of limb | postoperative loss of limb | bilateral amputee | amputee Includes: postoperative loss of limb | post traumatic loss of limb Excludes: Other acquired deformities of limbs | Congenital absence of thigh or lower leg with foot present | Congenital absence of both lower leg and foot [DB30.2] Adhesions of large intestine with obstruction Definition: Large bowel obstruction resulting from intraabdominal adhesion due to laparotomy, trauma, and intraabdominal inflammation such as endometriosis. Also known as: Adhesions of large intestine with obstruction | Postoperative obstruction of the large intestine [MG30.21] Chronic postsurgical pain Definition: Chronic postsurgical pain is chronic pain developing or increasing in intensity after a surgical procedure and persisting beyond the healing process, i.e. at least 3 months after surgery. The pain is either localised to the surgical field, projected to the innervation territory of a nerve situated in this area, or referred to a dermatome (after surgery/injury to deep somatic or visceral tissues). Other causes of pain including infection, malignancy etc. need to be excluded as well as pain contin Also known as: Chronic postsurgical pain | postsurgical pain | chronic postoperative pain | chronic postamputation pain | Chronic pain after spinal surgery Includes: Chronic pain after spinal surgery | Chronic pain after herniotomy | Chronic pain after hysterectomy === GRAPH WALKS === --- Walk 1 --- [MD11.1] Asphyxia Def: Asphyxia is a life-threatening condition in which oxygen is prevented from reaching the tissues by obstruction of or damage to any part of the respiratory system. More generally the term indicates all... --EXCLUDES--> [?] Foreign body in respiratory tract --CHILD--> [?] Foreign body in nasal sinus --- Walk 2 --- [MD11.1] Asphyxia Def: Asphyxia is a life-threatening condition in which oxygen is prevented from reaching the tissues by obstruction of or damage to any part of the respiratory system. More generally the term indicates all... --EXCLUDES--> [?] 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... --EXCLUDES--> [?] Stress fracture, not elsewhere classified --- 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... --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 4 --- [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 substance use Def: Disorders due to substance use include disorders that result from a single occasion or repeated use of substances that have psychoactive properties, including certain medications. Disorders related to... --- Walk 5 --- [3A51.7] High affinity haemoglobin Def: A disease caused by determinants arising after birth, in the antenatal period or by genetically inherited factors leading to high oxygen affinity haemoglobin. This disease is characterised by abnormal... --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 ... --PARENT--> [?] Anaemias or other erythrocyte disorders --- Walk 6 --- [3A51.7] High affinity haemoglobin Def: A disease caused by determinants arising after birth, in the antenatal period or by genetically inherited factors leading to high oxygen affinity haemoglobin. This disease is characterised by abnormal... --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...
[ "[MD11.1] Asphyxia\n Def: Asphyxia is a life-threatening condition in which oxygen is prevented from reaching the tissues by obstruction of or damage to any part of the respiratory system. More generally the term indicates all...\n --EXCLUDES--> [?] Foreign body in respiratory tract\n --CHILD--> [?] Foreign body in nasal sinus", "[MD11.1] Asphyxia\n Def: Asphyxia is a life-threatening condition in which oxygen is prevented from reaching the tissues by obstruction of or damage to any part of the respiratory system. More generally the term indicates all...\n --EXCLUDES--> [?] 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...\n --EXCLUDES--> [?] Stress fracture, not elsewhere classified", "[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 ...", "[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 substance use\n Def: Disorders due to substance use include disorders that result from a single occasion or repeated use of substances that have psychoactive properties, including certain medications. Disorders related to...", "[3A51.7] High affinity haemoglobin\n Def: A disease caused by determinants arising after birth, in the antenatal period or by genetically inherited factors leading to high oxygen affinity haemoglobin. This disease is characterised by abnormal...\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 --PARENT--> [?] Anaemias or other erythrocyte disorders", "[3A51.7] High affinity haemoglobin\n Def: A disease caused by determinants arising after birth, in the antenatal period or by genetically inherited factors leading to high oxygen affinity haemoglobin. This disease is characterised by abnormal...\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..." ]
MD11.1
Asphyxia
[ { "from_icd11": "MD11.1", "icd10_code": "R0901", "icd10_title": "Asphyxia" }, { "from_icd11": "MD11.1", "icd10_code": "R0902", "icd10_title": "Hypoxemia" }, { "from_icd11": "MD11.1", "icd10_code": "R090", "icd10_title": "Asphyxia and hypoxemia" }, { "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" } ]
R0901
Asphyxia
The diagnostic considerations in this case encompassed neoplasms consist of epidermoid cells, including poorly differentiated mucoepidermoid carcinoma, nonkeratinizing squamous cell carcinoma, and neuroendocrine carcinoma. Histologically, poorly differentiated mucoepidermoid carcinoma exhibited a solid growth pattern with a decreased presence of mucous cells and an increased abundance of epidermoid cells, demonstrating heightened cytologic atypia, necrosis, and perineural invasion. Mucoepidermoid carcinoma typically displayed robust positivity for KRT7 and negativity for KRT19. Additionally, a majority of mucoepidermoid carcinoma harbored rearrangement in the MAML2 gene. Nonkeratinizing squamous cell carcinoma was characterized by its relative immaturity, minimal to no keratinization, nuclear atypia, numerous mitotic figures, and peripheral palisading of tumor nuclei. The tumor comprised interconnecting squamous sheets that invade the stroma with a broad, pushing border. Immunohistochemically, nonkeratinizing squamous cell carcinoma was positive for high-molecular-weight cytokeratin, p63, and p40. Neuroendocrine carcinoma was composed of cells with hyperchromatic nuclei, indistinct nucleoli, and scant cytoplasm. The presence of numerous mitoses and apoptotic cells is notable. At least one neuroendocrine marker, such as Syn, CgA, or CD56, was typically immunopositive in neuroendocrine carcinomas.
4.417969
0.673828
sec[2]/p[3]
en
0.999996
PMC11320854
https://doi.org/10.1186/s13000-024-01530-0
[ "carcinoma", "cells", "mucoepidermoid", "squamous", "neuroendocrine", "nonkeratinizing", "cell", "epidermoid", "poorly", "differentiated" ]
[ { "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": "MF9Y", "title": "Other specified clinical findings on examination of urine, without diagnosis" }, { "code": "5C56.20", "title": "Mucolipidosis" }, { "code": "3A51.1", "title": "Sickle cell disease without crisis" }, { "code": "9A96.3", "title": "Primary anterior uveitis" }, { "code": "3A61.Z", "title": "Acquired pure red cell aplasia, unspecified" } ]
=== 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 [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) [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] [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 === GRAPH WALKS === --- Walk 1 --- [2D41] Unspecified carcinoma of unspecified site --PARENT--> [?] Malignant neoplasms of ill-defined or unspecified primary sites --PARENT--> [?] Malignant neoplasms, except primary neoplasms of lymphoid, haematopoietic, central nervous system or related tissues --- Walk 2 --- [2D41] Unspecified carcinoma of unspecified site --PARENT--> [?] Malignant neoplasms of ill-defined or unspecified primary sites --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 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... --CHILD--> [2C30] Melanoma of skin Def: A primary melanoma arising from atypical melanocytes in the skin. Precursor lesions include acquired and congenital melanocytic nevi, and dysplastic nevi. Several histologic variants have been recogni... --- 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--> [?] Carcinoma in situ of skin Def: Stage 0 includes: Tis, N0, M0. Tis: Carcinoma in situ. N0: No regional lymph node metastasis. M0: No clinical or radiographic evidence of distant metastasis.... --- 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 --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....
[ "[2D41] Unspecified carcinoma of unspecified site\n --PARENT--> [?] Malignant neoplasms of ill-defined or unspecified primary sites\n --PARENT--> [?] Malignant neoplasms, except primary neoplasms of lymphoid, haematopoietic, central nervous system or related tissues", "[2D41] Unspecified carcinoma of unspecified site\n --PARENT--> [?] Malignant neoplasms of ill-defined or unspecified primary sites\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...", "[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 --CHILD--> [2C30] Melanoma of skin\n Def: A primary melanoma arising from atypical melanocytes in the skin. Precursor lesions include acquired and congenital melanocytic nevi, and dysplastic nevi. Several histologic variants have been recogni...", "[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--> [?] Carcinoma in situ of skin\n Def: Stage 0 includes: Tis, N0, M0. Tis: Carcinoma in situ. N0: No regional lymph node metastasis. M0: No clinical or radiographic evidence of distant metastasis....", "[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 --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...." ]
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": "3A51.1", "icd10_code": "D571", "icd10_title": "Sickle-cell disease without crisis" }, { "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]" } ]
D098
Carcinoma in situ of other specified sites
Place the patient in the lateral position and mark the right mid-axillary line at the 8th intercostal for the observation port. An artificial pneumothorax was created with CO2 insufflation at a pressure of 10-12 mmHg. Under thoracoscopic guidance, surgical and auxiliary surgical ports were placed in the 3rd and 6th intercostal spaces on the midaxillary line and in the 6th intercostal space on the subscapularis angular line. With the assistance of thoracoscopy, the umbilical vein arch was ligated using vascular clips and ultrasonic knife, the esophageal lesion was mobilized. Thoracic duct ligation was performed, and lymph nodes were cleared adjacent to the esophagus, carinae area, and right and left recurrent laryngeal nerves. Negative-pressure drains were placed in the mediastinal and thoracic. Subsequently, in the supine position, an observation hole was made approximately 1.0 cm below the navel to establish an artificial pneumoperitoneum. Surgical ports were created on both the right and left sides of the navel, adjacent to the rectus abdominis muscle and below the rib arch along the midclavicular line. The stomach was mobilized, and the abdominal lymphadenectomy was performed. Under laparoscopic guidance, a tubular stomach was created from the lesser curvature. An incision was made at the anterior border of the left sternocleidomastoid muscle and an esophagogastric anastomosis was performed .
3.984375
0.679199
sec[1]/sec[1]/sec[0]/p[5]
en
0.999997
PMC11782036
https://doi.org/10.3389/fonc.2024.1426592
[ "line", "intercostal", "created", "position", "observation", "artificial", "pressure", "guidance", "ports", "arch" ]
[ { "code": "FB86.0", "title": "Epiphyseal arrest" }, { "code": "9A78.1", "title": "Corneal pigmentations or deposits" }, { "code": "6D11.5", "title": "Borderline pattern" }, { "code": "EE10.1Y", "title": "Other specified abnormality of nail surface" }, { "code": "PK91.16", "title": "Cardiovascular devices associated with injury or harm: peripheral venous catheter" }, { "code": "8C12.0", "title": "Intercostal neuropathy" }, { "code": "8E43.Y", "title": "Other specified pain disorders" }, { "code": "ME81.0", "title": "Intercostal pain" }, { "code": "NB30.50", "title": "Laceration of intercostal blood vessels" }, { "code": "NB30.5Z", "title": "Injury of intercostal blood vessels, unspecified" } ]
=== ICD-11 CODES FOUND === [FB86.0] Epiphyseal arrest Also known as: Epiphyseal arrest | Harris lines | Atraumatic epiphyseal arrest | Epiphyseal arrest due to hormone disorders | Epiphyseal arrest due to kidney disease [9A78.1] Corneal pigmentations or deposits Also known as: Corneal pigmentations or deposits | Haematocornea | corneal blood staining | keratohaemia | Kayser-Fleischer ring Includes: Haematocornea | Kayser-Fleischer ring | Krukenberg spindle [6D11.5] Borderline pattern Definition: The Borderline pattern specifier may be applied to individuals whose pattern of personality disturbance is characterised by a pervasive pattern of instability of interpersonal relationships, self-image, and affects, and marked impulsivity, as indicated by many of the following: Frantic efforts to avoid real or imagined abandonment; A pattern of unstable and intense interpersonal relationships; Identity disturbance, manifested in markedly and persistently unstable self-image or sense of self; A t Also known as: Borderline pattern [EE10.1Y] Other specified abnormality of nail surface Also known as: Other specified abnormality of nail surface | Longitudinal ridging of nails | Beaded nails | Trachyonychia | Median nail dystrophy [PK91.16] Cardiovascular devices associated with injury or harm: peripheral venous catheter Also known as: Cardiovascular devices associated with injury or harm: peripheral venous catheter | complication of intravenous line | IV - [intravenous] line complication Excludes: Circumstances associated with a surgical or other medical device influencing the episode of care without injury or harm [8C12.0] Intercostal neuropathy Definition: Peripheral neuropathy of the intercostal nerves Also known as: Intercostal neuropathy | disease of intercostal nerve | disorder of intercostal nerve [8E43.Y] Other specified pain disorders Also known as: Other specified pain disorders | Paroxysmal extreme pain disorder | Rectus abdominis syndrome | Kómár syndrome | Intercostal nerve syndrome [ME81.0] Intercostal pain Also known as: Intercostal pain Excludes: Chronic primary musculoskeletal pain | Chronic secondary musculoskeletal pain [NB30.50] Laceration of intercostal blood vessels Also known as: Laceration of intercostal blood vessels [NB30.5Z] Injury of intercostal blood vessels, unspecified Also known as: Injury of intercostal blood vessels, unspecified | Injury of intercostal blood vessels === GRAPH WALKS === --- Walk 1 --- [FB86.0] Epiphyseal arrest --PARENT--> [FB86] Disorders associated with bone growth --PARENT--> [?] Osteopathies or chondropathies --- Walk 2 --- [FB86.0] Epiphyseal arrest --PARENT--> [FB86] Disorders associated with bone growth --CHILD--> [FB86.1] Bone hyperplasias --- Walk 3 --- [9A78.1] Corneal pigmentations or deposits --PARENT--> [9A78] Certain specified disorders of cornea --CHILD--> [9A78.2] Corneal oedema --- Walk 4 --- [9A78.1] Corneal pigmentations or deposits --PARENT--> [9A78] Certain specified disorders of cornea --RELATED_TO--> [?] Ocular laceration or rupture with prolapse or loss of intraocular tissue, unilateral Def: Forcible or traumatic tearing or breaking of the eyeball with protrusion or loss of the tissues and fluids located within the eyeball.... --- Walk 5 --- [6D11.5] Borderline pattern Def: The Borderline pattern specifier may be applied to individuals whose pattern of personality disturbance is characterised by a pervasive pattern of instability of interpersonal relationships, self-imag... --PARENT--> [6D11] Prominent personality traits or patterns Def: Trait domain qualifiers may be applied to Personality Disorders or Personality Difficulty to describe the characteristics of the individual’s personality that are most prominent and that contribute to... --CHILD--> [6D11.2] Dissociality in personality disorder or personality difficulty Def: The core feature of the Dissociality trait domain is disregard for the rights and feelings of others, encompassing both self-centeredness and lack of empathy. Common manifestations of Dissociality, no... --- Walk 6 --- [6D11.5] Borderline pattern Def: The Borderline pattern specifier may be applied to individuals whose pattern of personality disturbance is characterised by a pervasive pattern of instability of interpersonal relationships, self-imag... --PARENT--> [6D11] Prominent personality traits or patterns Def: Trait domain qualifiers may be applied to Personality Disorders or Personality Difficulty to describe the characteristics of the individual’s personality that are most prominent and that contribute to... --CHILD--> [6D11.1] Detachment in personality disorder or personality difficulty Def: The core feature of the Detachment trait domain is the tendency to maintain interpersonal distance (social detachment) and emotional distance (emotional detachment). Common manifestations of Detachmen...
[ "[FB86.0] Epiphyseal arrest\n --PARENT--> [FB86] Disorders associated with bone growth\n --PARENT--> [?] Osteopathies or chondropathies", "[FB86.0] Epiphyseal arrest\n --PARENT--> [FB86] Disorders associated with bone growth\n --CHILD--> [FB86.1] Bone hyperplasias", "[9A78.1] Corneal pigmentations or deposits\n --PARENT--> [9A78] Certain specified disorders of cornea\n --CHILD--> [9A78.2] Corneal oedema", "[9A78.1] Corneal pigmentations or deposits\n --PARENT--> [9A78] Certain specified disorders of cornea\n --RELATED_TO--> [?] Ocular laceration or rupture with prolapse or loss of intraocular tissue, unilateral\n Def: Forcible or traumatic tearing or breaking of the eyeball with protrusion or loss of the tissues and fluids located within the eyeball....", "[6D11.5] Borderline pattern\n Def: The Borderline pattern specifier may be applied to individuals whose pattern of personality disturbance is characterised by a pervasive pattern of instability of interpersonal relationships, self-imag...\n --PARENT--> [6D11] Prominent personality traits or patterns\n Def: Trait domain qualifiers may be applied to Personality Disorders or Personality Difficulty to describe the characteristics of the individual’s personality that are most prominent and that contribute to...\n --CHILD--> [6D11.2] Dissociality in personality disorder or personality difficulty\n Def: The core feature of the Dissociality trait domain is disregard for the rights and feelings of others, encompassing both self-centeredness and lack of empathy. Common manifestations of Dissociality, no...", "[6D11.5] Borderline pattern\n Def: The Borderline pattern specifier may be applied to individuals whose pattern of personality disturbance is characterised by a pervasive pattern of instability of interpersonal relationships, self-imag...\n --PARENT--> [6D11] Prominent personality traits or patterns\n Def: Trait domain qualifiers may be applied to Personality Disorders or Personality Difficulty to describe the characteristics of the individual’s personality that are most prominent and that contribute to...\n --CHILD--> [6D11.1] Detachment in personality disorder or personality difficulty\n Def: The core feature of the Detachment trait domain is the tendency to maintain interpersonal distance (social detachment) and emotional distance (emotional detachment). Common manifestations of Detachmen..." ]
FB86.0
Epiphyseal arrest
[ { "from_icd11": "FB86.0", "icd10_code": "M891", "icd10_title": "Physeal arrest" }, { "from_icd11": "9A78.1", "icd10_code": "H18049", "icd10_title": "Kayser-Fleischer ring, unspecified eye" }, { "from_icd11": "9A78.1", "icd10_code": "H180", "icd10_title": "Corneal pigmentations and deposits" }, { "from_icd11": "PK91.16", "icd10_code": "T8242XA", "icd10_title": "Displacement of vascular dialysis catheter, initial encounter" }, { "from_icd11": "PK91.16", "icd10_code": "T8249XD", "icd10_title": "Other complication of vascular dialysis catheter, subsequent encounter" }, { "from_icd11": "PK91.16", "icd10_code": "T8243XA", "icd10_title": "Leakage of vascular dialysis catheter, initial encounter" }, { "from_icd11": "PK91.16", "icd10_code": "T824", "icd10_title": "Mechanical complication of vascular dialysis catheter" }, { "from_icd11": "8C12.0", "icd10_code": "G580", "icd10_title": "Intercostal neuropathy" }, { "from_icd11": "ME81.0", "icd10_code": "R073", "icd10_title": "" }, { "from_icd11": "NB30.5Z", "icd10_code": "S25512A", "icd10_title": "Laceration of intercostal blood vessels, left side, initial encounter" }, { "from_icd11": "NB30.5Z", "icd10_code": "S25501A", "icd10_title": "Unspecified injury of intercostal blood vessels, right side, initial encounter" }, { "from_icd11": "NB30.5Z", "icd10_code": "S25502A", "icd10_title": "Unspecified injury of intercostal blood vessels, left side, initial encounter" }, { "from_icd11": "NB30.5Z", "icd10_code": "S25509A", "icd10_title": "Unspecified injury of intercostal blood vessels, unspecified side, initial encounter" }, { "from_icd11": "NB30.5Z", "icd10_code": "S255", "icd10_title": "Injury of intercostal blood vessels" } ]
M891
Physeal arrest
We present the case of a 38-year-old male undergoing HD with a history of end-stage renal disease (ESRD) secondary to autosomal dominant polycystic kidney disease on renal replacement therapy (RRT) for the last 18 years. Other past medical history included arterial hypertension, secondary osteoporosis due to secondary hyperparathyroidism, and virus C hepatitis. At 35 years of age, due to markedly elevated PTH levels reaching 2100 pg/mL (normal range in general population 15–65 pg/mL) despite optimal medical treatment, he underwent total PTx, resulting in an initial reduction of PTH to 330 pg/mL and the onset of severe hypocalcemia. Following the administration of calcium supplements and vitamin D analogs, the patient developed painful necrotic plaques on the fingers, which were subsequently diagnosed as classic calciphylaxis lesions . After a thorough evaluation of clinical features and underlying comorbidities, differential diagnosis was made with livedo reticularis, cholesterol embolism, pyoderma gangrenosum, and vasculitis. Consequently, it was decided to postpone calcium and vitamin D supplementation and a skin biopsy was considered. However, the spontaneous resolution of ischemic skin lesions after discontinuing calcium supplements in the absence of inflammatory syndrome, anticoagulation or eosinophilia supported the diagnosis of CUA and led to reconsideration of the need for a skin biopsy.
4.035156
0.979004
sec[1]/p[0]
en
0.999999
PMC11940037
https://doi.org/10.3390/biomedicines13030715
[ "calcium", "skin", "renal", "supplements", "vitamin", "lesions", "biopsy", "present", "undergoing", "stage" ]
[ { "code": "5B5K.1Z", "title": "Calcium deficiency, unspecified" }, { "code": "5B91.0", "title": "Hypercalcaemia" }, { "code": "5B5K.1Y", "title": "Other specified calcium deficiency" }, { "code": "5C64.5", "title": "Disorders of calcium metabolism" }, { "code": "FB40.Y", "title": "Other specified tenosynovitis" }, { "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 === [5B5K.1Z] Calcium deficiency, unspecified Also known as: Calcium deficiency, unspecified | Calcium deficiency | hypocalcaemia NOS | disturbance of calcium absorption | disorder of calcium absorption [5B91.0] Hypercalcaemia Definition: Hypercalcaemia is a condition caused by increased calcium levels. The higher the calcium levels and the faster its level rises, the more severe will be the symptoms. When present, symptoms are caused by dehydration secondary to urinary losses of calcium, water and other electrolytes, and to an increase in membrane potential caused by the elevation in extracellular fluid ionized calcium concentration. Patients with moderate to severe hypercalcaemia often complain of nausea and vomiting, symptoms Also known as: Hypercalcaemia | Calcium excess | elevated serum calcium | hypercalcaemic crisis | hypercalcaemic syndrome [5B5K.1Y] Other specified calcium deficiency Also known as: Other specified calcium deficiency | Dietary hypocalcaemia | dietary calcium deficiency [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 [FB40.Y] Other specified tenosynovitis Also known as: Other specified tenosynovitis | Other tenosynovitis or tendinitis | synovitis NOS | Bicipital tendinitis | biceps tendinitis [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 --- [5B5K.1Z] Calcium deficiency, unspecified --PARENT--> [5B5K.1] Calcium deficiency Def: Hypocalcaemia is defined as a total serum calcium concentration of less than 8.4 mg/dl (2.1 mmol/litre) or an ionized calcium concentration of less than 4.48 mg/dl (1.12 mmol/litre). There are numerou... --CHILD--> [5B5K.1Y] Other specified calcium deficiency --- Walk 2 --- [5B5K.1Z] Calcium deficiency, unspecified --PARENT--> [5B5K.1] Calcium deficiency Def: Hypocalcaemia is defined as a total serum calcium concentration of less than 8.4 mg/dl (2.1 mmol/litre) or an ionized calcium concentration of less than 4.48 mg/dl (1.12 mmol/litre). There are numerou... --RELATED_TO--> [?] Neonatal hypocalcaemia Def: Hypocalcaemia is a common metabolic problem in newborns. In the neonate, hypocalcaemia is defined by birth weight (BW) categories. In infants with BW greater than 1500 g, hypocalcaemia is defined as a... --- Walk 3 --- [5B91.0] Hypercalcaemia Def: Hypercalcaemia is a condition caused by increased calcium levels. The higher the calcium levels and the faster its level rises, the more severe will be the symptoms. When present, symptoms are caused ... --PARENT--> [5B91] Mineral excesses --RELATED_TO--> [?] Hyperkalaemia --- Walk 4 --- [5B91.0] Hypercalcaemia Def: Hypercalcaemia is a condition caused by increased calcium levels. The higher the calcium levels and the faster its level rises, the more severe will be the symptoms. When present, symptoms are caused ... --RELATED_TO--> [?] Myopathy due to hypercalcaemia --PARENT--> [?] Hypercalcaemia Def: Hypercalcaemia is a condition caused by increased calcium levels. The higher the calcium levels and the faster its level rises, the more severe will be the symptoms. When present, symptoms are caused ... --- Walk 5 --- [5B5K.1Y] Other specified calcium deficiency --PARENT--> [5B5K.1] Calcium deficiency Def: Hypocalcaemia is defined as a total serum calcium concentration of less than 8.4 mg/dl (2.1 mmol/litre) or an ionized calcium concentration of less than 4.48 mg/dl (1.12 mmol/litre). There are numerou... --RELATED_TO--> [?] Neonatal hypocalcaemia Def: Hypocalcaemia is a common metabolic problem in newborns. In the neonate, hypocalcaemia is defined by birth weight (BW) categories. In infants with BW greater than 1500 g, hypocalcaemia is defined as a... --- Walk 6 --- [5B5K.1Y] Other specified calcium deficiency --PARENT--> [5B5K.1] Calcium deficiency Def: Hypocalcaemia is defined as a total serum calcium concentration of less than 8.4 mg/dl (2.1 mmol/litre) or an ionized calcium concentration of less than 4.48 mg/dl (1.12 mmol/litre). There are numerou... --RELATED_TO--> [?] Neonatal hypocalcaemia Def: Hypocalcaemia is a common metabolic problem in newborns. In the neonate, hypocalcaemia is defined by birth weight (BW) categories. In infants with BW greater than 1500 g, hypocalcaemia is defined as a...
[ "[5B5K.1Z] Calcium deficiency, unspecified\n --PARENT--> [5B5K.1] Calcium deficiency\n Def: Hypocalcaemia is defined as a total serum calcium concentration of less than 8.4 mg/dl (2.1 mmol/litre) or an ionized calcium concentration of less than 4.48 mg/dl (1.12 mmol/litre). There are numerou...\n --CHILD--> [5B5K.1Y] Other specified calcium deficiency", "[5B5K.1Z] Calcium deficiency, unspecified\n --PARENT--> [5B5K.1] Calcium deficiency\n Def: Hypocalcaemia is defined as a total serum calcium concentration of less than 8.4 mg/dl (2.1 mmol/litre) or an ionized calcium concentration of less than 4.48 mg/dl (1.12 mmol/litre). There are numerou...\n --RELATED_TO--> [?] Neonatal hypocalcaemia\n Def: Hypocalcaemia is a common metabolic problem in newborns. In the neonate, hypocalcaemia is defined by birth weight (BW) categories. In infants with BW greater than 1500 g, hypocalcaemia is defined as a...", "[5B91.0] Hypercalcaemia\n Def: Hypercalcaemia is a condition caused by increased calcium levels. The higher the calcium levels and the faster its level rises, the more severe will be the symptoms. When present, symptoms are caused ...\n --PARENT--> [5B91] Mineral excesses\n --RELATED_TO--> [?] Hyperkalaemia", "[5B91.0] Hypercalcaemia\n Def: Hypercalcaemia is a condition caused by increased calcium levels. The higher the calcium levels and the faster its level rises, the more severe will be the symptoms. When present, symptoms are caused ...\n --RELATED_TO--> [?] Myopathy due to hypercalcaemia\n --PARENT--> [?] Hypercalcaemia\n Def: Hypercalcaemia is a condition caused by increased calcium levels. The higher the calcium levels and the faster its level rises, the more severe will be the symptoms. When present, symptoms are caused ...", "[5B5K.1Y] Other specified calcium deficiency\n --PARENT--> [5B5K.1] Calcium deficiency\n Def: Hypocalcaemia is defined as a total serum calcium concentration of less than 8.4 mg/dl (2.1 mmol/litre) or an ionized calcium concentration of less than 4.48 mg/dl (1.12 mmol/litre). There are numerou...\n --RELATED_TO--> [?] Neonatal hypocalcaemia\n Def: Hypocalcaemia is a common metabolic problem in newborns. In the neonate, hypocalcaemia is defined by birth weight (BW) categories. In infants with BW greater than 1500 g, hypocalcaemia is defined as a...", "[5B5K.1Y] Other specified calcium deficiency\n --PARENT--> [5B5K.1] Calcium deficiency\n Def: Hypocalcaemia is defined as a total serum calcium concentration of less than 8.4 mg/dl (2.1 mmol/litre) or an ionized calcium concentration of less than 4.48 mg/dl (1.12 mmol/litre). There are numerou...\n --RELATED_TO--> [?] Neonatal hypocalcaemia\n Def: Hypocalcaemia is a common metabolic problem in newborns. In the neonate, hypocalcaemia is defined by birth weight (BW) categories. In infants with BW greater than 1500 g, hypocalcaemia is defined as a..." ]
5B5K.1Z
Calcium deficiency, unspecified
[ { "from_icd11": "5B5K.1Z", "icd10_code": "E58", "icd10_title": "Dietary calcium deficiency" }, { "from_icd11": "5C64.5", "icd10_code": "E8352", "icd10_title": "Hypercalcemia" }, { "from_icd11": "5C64.5", "icd10_code": "E8351", "icd10_title": "Hypocalcemia" }, { "from_icd11": "5C64.5", "icd10_code": "E8359", "icd10_title": "Other disorders of calcium metabolism" }, { "from_icd11": "5C64.5", "icd10_code": "E8350", "icd10_title": "Unspecified disorder of calcium metabolism" }, { "from_icd11": "5C64.5", "icd10_code": "E835", "icd10_title": "Disorders of calcium metabolism" }, { "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" } ]
E58
Dietary calcium deficiency
The eosinophil performs its functions largely through its mediators, in which the main effects include participating in the body’s defense against helminthic parasites and inflammatory responses in general, regulating homeostasis in certain circumstances, such as wound healing and mammary gland development . However, eosinophilic inflammation can cause severe tissue damage in some situations, especially AEC > 1.5x10 3 /μL. There are various causes of eosinophilia/HE, including clonal HE and reactive HE. Reactive or secondary eosinophilia encompasses all medical conditions and disease states (including infections, allergic diseases, primary immunodeficiency, autoimmune diseases, malignancies, drug reactions, etc.) . The patient did not have manifestations of these diseases and did not have risk factors for infections of parasites. He had a positive dengue IgM ELISA that was performed on the 13th day after admission (or the 18th day after the onset of the first symptoms). Based on the epidemiology and clinical features of the patient, it can be confirmed that he could not develop these diseases. Therefore, dengue infection was the most likely cause because of the popularity of the virus in southern Vietnam. Eosinophilia can be found in dengue infection . Dengue-associated stroke has also been reported (ischemic or hemorrhagic stroke) as an infrequent neurological complication of dengue infection .
4.167969
0.495117
sec[2]/p[1]
en
0.999997
PMC11310897
https://doi.org/10.7759/cureus.64220
[ "dengue", "diseases", "eosinophilia", "infection", "parasites", "cause", "including", "reactive", "infections", "these" ]
[ { "code": "1D2Z", "title": "Dengue fever, unspecified" }, { "code": "1D22", "title": "Severe dengue" }, { "code": "1D21", "title": "Dengue with warning signs" }, { "code": "1D20", "title": "Dengue without warning signs" }, { "code": "QA08.5", "title": "Special screening examination for other viral diseases" }, { "code": "FB3Z", "title": "Disorders of muscles, unspecified" }, { "code": "FA5Z", "title": "Arthropathies, unspecified" }, { "code": "1D9Z", "title": "Unspecified viral infection of unspecified site" }, { "code": "1E1Z", "title": "Unspecified viral disease" }, { "code": "FC0Z", "title": "Diseases of the musculoskeletal system or connective tissue, unspecified" } ]
=== ICD-11 CODES FOUND === [1D2Z] Dengue fever, unspecified Also known as: Dengue fever, unspecified | breakbone fever | classical dengue | classical dengue fever | dandy fever [1D22] Severe dengue Definition: Clinical signs include: 1. Severe plasma leakage leading to shock (dengue shock syndrome - DSS) and/or fluid accumulation with respiratory distress; 2. severe bleeding as evaluated by clinician, 3. severe organ involvement: Liver AST or ALT ≥ 1000, CNS: impaired consciousness, involvement of other organs, as myocarditis or nephritis. Also known as: Severe dengue | Severe dengue haemorrhagic fever | Severe dengue fever | dengue shock syndrome | Encephalitis due to Dengue fever [1D21] Dengue with warning signs Definition: Clinical warning signs are: abdominal pain or tenderness, mucosal bleeding, lethargy and/or restlessness, rapid decrease in platelet count, increase in haematocrit. Other signs can include: persistent vomiting, visible fluid accumulation, liver enlargement more than 2 cm. Also known as: Dengue with warning signs | Bangkok haemorrhagic fever | Singapore haemorrhagic fever | Thailand haemorrhagic fever | Southeast Asia haemorrhagic fever [1D20] Dengue without warning signs Also known as: Dengue without warning signs | Dengue fever without warning signs | Dengue haemorrhagic fever Grade 1 | Dengue haemorrhagic fever without warning signs Includes: Dengue haemorrhagic fever Grade 1 | Dengue fever without warning signs | Dengue haemorrhagic fever without warning signs [QA08.5] Special screening examination for other viral diseases Also known as: Special screening examination for other viral diseases | Measles screening | Poliomyelitis screening | Rubella screening | Screening for Dengue fever Includes: Screening for COVID-19 Excludes: Viral intestinal infections | Special screening examination for infections with a predominantly sexual mode of transmission | Special screening examination for human immunodeficiency virus [FB3Z] Disorders of muscles, unspecified Also known as: Disorders of muscles, unspecified | disorder of muscle, unspecified | muscle disease | muscular disease | muscular disorder [FA5Z] Arthropathies, unspecified Also known as: Arthropathies, unspecified | Disorders affecting predominantly peripheral joints | Disorders affecting predominantly peripheral limb joints | arthropathy NOS | arthropathic [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 [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 === GRAPH WALKS === --- Walk 1 --- [1D2Z] Dengue fever, unspecified --PARENT--> [?] Dengue Def: Dengue is a viral disease transmitted by the bite of a mosquito infected by dengue viruses. It is one disease entity with different clinical presentations and often with unpredictable clinical evoluti... --CHILD--> [1D20] Dengue without warning signs --- Walk 2 --- [1D2Z] Dengue fever, unspecified --PARENT--> [?] Dengue Def: Dengue is a viral disease transmitted by the bite of a mosquito infected by dengue viruses. It is one disease entity with different clinical presentations and often with unpredictable clinical evoluti... --CHILD--> [1D20] Dengue without warning signs --- Walk 3 --- [1D22] Severe dengue Def: Clinical signs include: 1. Severe plasma leakage leading to shock (dengue shock syndrome - DSS) and/or fluid accumulation with respiratory distress; 2. severe bleeding as evaluated by clinician, 3. se... --PARENT--> [?] Dengue Def: Dengue is a viral disease transmitted by the bite of a mosquito infected by dengue viruses. It is one disease entity with different clinical presentations and often with unpredictable clinical evoluti... --CHILD--> [1D21] Dengue with warning signs Def: Clinical warning signs are: abdominal pain or tenderness, mucosal bleeding, lethargy and/or restlessness, rapid decrease in platelet count, increase in haematocrit. Other signs can include: persistent... --- Walk 4 --- [1D22] Severe dengue Def: Clinical signs include: 1. Severe plasma leakage leading to shock (dengue shock syndrome - DSS) and/or fluid accumulation with respiratory distress; 2. severe bleeding as evaluated by clinician, 3. se... --PARENT--> [?] Dengue Def: Dengue is a viral disease transmitted by the bite of a mosquito infected by dengue viruses. It is one disease entity with different clinical presentations and often with unpredictable clinical evoluti... --CHILD--> [1D21] Dengue with warning signs Def: Clinical warning signs are: abdominal pain or tenderness, mucosal bleeding, lethargy and/or restlessness, rapid decrease in platelet count, increase in haematocrit. Other signs can include: persistent... --- Walk 5 --- [1D21] Dengue with warning signs Def: Clinical warning signs are: abdominal pain or tenderness, mucosal bleeding, lethargy and/or restlessness, rapid decrease in platelet count, increase in haematocrit. Other signs can include: persistent... --PARENT--> [?] Dengue Def: Dengue is a viral disease transmitted by the bite of a mosquito infected by dengue viruses. It is one disease entity with different clinical presentations and often with unpredictable clinical evoluti... --CHILD--> [1D21] Dengue with warning signs Def: Clinical warning signs are: abdominal pain or tenderness, mucosal bleeding, lethargy and/or restlessness, rapid decrease in platelet count, increase in haematocrit. Other signs can include: persistent... --- Walk 6 --- [1D21] Dengue with warning signs Def: Clinical warning signs are: abdominal pain or tenderness, mucosal bleeding, lethargy and/or restlessness, rapid decrease in platelet count, increase in haematocrit. Other signs can include: persistent... --PARENT--> [?] Dengue Def: Dengue is a viral disease transmitted by the bite of a mosquito infected by dengue viruses. It is one disease entity with different clinical presentations and often with unpredictable clinical evoluti... --CHILD--> [1D21] Dengue with warning signs Def: Clinical warning signs are: abdominal pain or tenderness, mucosal bleeding, lethargy and/or restlessness, rapid decrease in platelet count, increase in haematocrit. Other signs can include: persistent...
[ "[1D2Z] Dengue fever, unspecified\n --PARENT--> [?] Dengue\n Def: Dengue is a viral disease transmitted by the bite of a mosquito infected by dengue viruses. It is one disease entity with different clinical presentations and often with unpredictable clinical evoluti...\n --CHILD--> [1D20] Dengue without warning signs", "[1D2Z] Dengue fever, unspecified\n --PARENT--> [?] Dengue\n Def: Dengue is a viral disease transmitted by the bite of a mosquito infected by dengue viruses. It is one disease entity with different clinical presentations and often with unpredictable clinical evoluti...\n --CHILD--> [1D20] Dengue without warning signs", "[1D22] Severe dengue\n Def: Clinical signs include: 1. Severe plasma leakage leading to shock (dengue shock syndrome - DSS) and/or fluid accumulation with respiratory distress; 2. severe bleeding as evaluated by clinician, 3. se...\n --PARENT--> [?] Dengue\n Def: Dengue is a viral disease transmitted by the bite of a mosquito infected by dengue viruses. It is one disease entity with different clinical presentations and often with unpredictable clinical evoluti...\n --CHILD--> [1D21] Dengue with warning signs\n Def: Clinical warning signs are: abdominal pain or tenderness, mucosal bleeding, lethargy and/or restlessness, rapid decrease in platelet count, increase in haematocrit. Other signs can include: persistent...", "[1D22] Severe dengue\n Def: Clinical signs include: 1. Severe plasma leakage leading to shock (dengue shock syndrome - DSS) and/or fluid accumulation with respiratory distress; 2. severe bleeding as evaluated by clinician, 3. se...\n --PARENT--> [?] Dengue\n Def: Dengue is a viral disease transmitted by the bite of a mosquito infected by dengue viruses. It is one disease entity with different clinical presentations and often with unpredictable clinical evoluti...\n --CHILD--> [1D21] Dengue with warning signs\n Def: Clinical warning signs are: abdominal pain or tenderness, mucosal bleeding, lethargy and/or restlessness, rapid decrease in platelet count, increase in haematocrit. Other signs can include: persistent...", "[1D21] Dengue with warning signs\n Def: Clinical warning signs are: abdominal pain or tenderness, mucosal bleeding, lethargy and/or restlessness, rapid decrease in platelet count, increase in haematocrit. Other signs can include: persistent...\n --PARENT--> [?] Dengue\n Def: Dengue is a viral disease transmitted by the bite of a mosquito infected by dengue viruses. It is one disease entity with different clinical presentations and often with unpredictable clinical evoluti...\n --CHILD--> [1D21] Dengue with warning signs\n Def: Clinical warning signs are: abdominal pain or tenderness, mucosal bleeding, lethargy and/or restlessness, rapid decrease in platelet count, increase in haematocrit. Other signs can include: persistent...", "[1D21] Dengue with warning signs\n Def: Clinical warning signs are: abdominal pain or tenderness, mucosal bleeding, lethargy and/or restlessness, rapid decrease in platelet count, increase in haematocrit. Other signs can include: persistent...\n --PARENT--> [?] Dengue\n Def: Dengue is a viral disease transmitted by the bite of a mosquito infected by dengue viruses. It is one disease entity with different clinical presentations and often with unpredictable clinical evoluti...\n --CHILD--> [1D21] Dengue with warning signs\n Def: Clinical warning signs are: abdominal pain or tenderness, mucosal bleeding, lethargy and/or restlessness, rapid decrease in platelet count, increase in haematocrit. Other signs can include: persistent..." ]
1D2Z
Dengue fever, unspecified
[ { "from_icd11": "1D2Z", "icd10_code": "A97", "icd10_title": "" }, { "from_icd11": "1D2Z", "icd10_code": "A979", "icd10_title": "" }, { "from_icd11": "1D22", "icd10_code": "A972", "icd10_title": "" }, { "from_icd11": "1D21", "icd10_code": "A971", "icd10_title": "" }, { "from_icd11": "1D20", "icd10_code": "A970", "icd10_title": "" }, { "from_icd11": "QA08.5", "icd10_code": "Z1159", "icd10_title": "Encounter for screening for other viral diseases" }, { "from_icd11": "QA08.5", "icd10_code": "Z1151", "icd10_title": "Encounter for screening for human papillomavirus (HPV)" }, { "from_icd11": "QA08.5", "icd10_code": "Z115", "icd10_title": "Encounter for screening for other viral diseases" }, { "from_icd11": "FB3Z", "icd10_code": "M60831", "icd10_title": "Other myositis, right forearm" }, { "from_icd11": "FB3Z", "icd10_code": "M60869", "icd10_title": "Other myositis, unspecified lower leg" }, { "from_icd11": "FB3Z", "icd10_code": "M60811", "icd10_title": "Other myositis, right shoulder" }, { "from_icd11": "FB3Z", "icd10_code": "M6080", "icd10_title": "Other myositis, unspecified site" }, { "from_icd11": "FB3Z", "icd10_code": "M60851", "icd10_title": "Other myositis, right thigh" }, { "from_icd11": "FB3Z", "icd10_code": "M6010", "icd10_title": "Interstitial myositis of unspecified site" }, { "from_icd11": "FB3Z", "icd10_code": "M6018", "icd10_title": "Interstitial myositis, other site" } ]
A97
Patient 1 (P1), born to non-consanguineous parents of Indigenous Canadian ancestry with a history of miscarriages, was diagnosed with a bifid uvula, exudative vitreous retinopathy, and developed atopic dermatitis and intractable seizures within the first year of life. Brain magnetic resonance imaging (MRI) showed bilateral polymicrogyria, delayed myelination, white matter loss, calcifications, dysplastic corpus callosum, enlarged ventricles, and microcephaly . Patient 2 (P2) was born at 33 wk gestation with intrauterine growth restriction and microcephaly to non-consanguineous parents. While P1 had more severe disease, both P1 and P2 had several overlapping clinical features (outlined in Table S1 ). These included developmental delay and vision defects, severe colitis recalcitrant to medical therapy requiring a colectomy in P1 , and immune dysregulation together with atopy features including chronic infections, atopic dermatitis, multiple allergies, elevated serum IgE levels, eosinophilia, and eosinophilic enteropathy . A third family was identified after four pregnancies were terminated due to brain malformations (fetuses F1–F4). Each fetus had multiple brain abnormalities including Dandy–Walker malformation, ventriculomegaly/hydrocephaly, posterior fossa cyst, and corpus callosum agenesis/hypoplasia. There were also other developmental defects including cleft palate and abdominal wall defects.
4.089844
0.821777
sec[1]/sec[0]/p[0]
en
0.999997
PMC11554753
https://doi.org/10.1084/jem.20240546
[ "brain", "defects", "including", "born", "consanguineous", "parents", "atopic", "dermatitis", "corpus", "callosum" ]
[ { "code": "8E7Y", "title": "Other specified diseases of the nervous system" }, { "code": "LA05.Z", "title": "Cerebral structural developmental anomalies, unspecified" }, { "code": "1D00.Z", "title": "Infectious encephalitis, unspecified" }, { "code": "LA00.0Z", "title": "Anencephaly, unspecified" }, { "code": "NA07.3Y", "title": "Other specified diffuse brain injury" }, { "code": "BE2Z", "title": "Diseases of the circulatory system, unspecified" }, { "code": "LD9Z", "title": "Developmental anomalies, unspecified" }, { "code": "5D2Z", "title": "Metabolic disorders, unspecified" }, { "code": "MC1Y", "title": "Other specified symptoms or signs involving the visual system" }, { "code": "AB52", "title": "Deafness not otherwise specified" } ]
=== ICD-11 CODES FOUND === [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 [LA05.Z] Cerebral structural developmental anomalies, unspecified Also known as: Cerebral structural developmental anomalies, unspecified | Cerebral structural developmental anomalies | Malformations of brain | brain abnormality NOS | brain deformity NOS [1D00.Z] Infectious encephalitis, unspecified Also known as: Infectious encephalitis, unspecified | Infectious encephalitis, not elsewhere classified | encephalitis NOS | acute encephalitis NOS | acute brain inflammation [LA00.0Z] Anencephaly, unspecified Also known as: Anencephaly, unspecified | Anencephaly | anencephalic monster | anencephalus | brain absence [NA07.3Y] Other specified diffuse brain injury Also known as: Other specified diffuse brain injury | Brain contusion | Cerebral contusion NOS | Diffuse cortex contusion | diffuse cortical contusion [BE2Z] Diseases of the circulatory system, unspecified Also known as: Diseases of the circulatory system, unspecified | circulatory disease NOS | cardiovascular disease NOS | cardiovascular system disease NOS | CVS - [cardiovascular system] disease [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 [5D2Z] Metabolic disorders, unspecified Also known as: Metabolic disorders, unspecified | metabolic abnormality | metabolic debility | metabolic defect | metabolic disruption [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 [AB52] Deafness not otherwise specified Also known as: Deafness not otherwise specified | deaf | hearing loss NOS | hearing impairment | hearing loss === GRAPH WALKS === --- Walk 1 --- [8E7Y] Other specified diseases of the nervous system --PARENT--> [08] Diseases of the nervous system Def: This is a group of conditions characterised as being in or associated with the nervous system.... --RELATED_TO--> [?] Syndromes with central nervous system anomalies as a major feature --- Walk 2 --- [8E7Y] Other specified diseases of the nervous system --PARENT--> [08] Diseases of the nervous system Def: This is a group of conditions characterised as being in or associated with the nervous system.... --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 3 --- [LA05.Z] Cerebral structural developmental anomalies, unspecified --PARENT--> [LA05] Cerebral structural developmental anomalies Def: Any condition caused by failure of the brain to correctly develop during the antenatal period.... --CHILD--> [LA05.1] Megalencephaly Def: A condition caused by failure of the brain to correctly develop during the antenatal period. This condition is characterised by increased size or weight of an otherwise correctly formed brain. This co... --- Walk 4 --- [LA05.Z] Cerebral structural developmental anomalies, unspecified --PARENT--> [LA05] Cerebral structural developmental anomalies Def: Any condition caused by failure of the brain to correctly develop during the antenatal period.... --EXCLUDES--> [?] Encephalocele --- Walk 5 --- [1D00.Z] Infectious encephalitis, unspecified --PARENT--> [1D00] Infectious encephalitis, not elsewhere classified Def: A disease of the brain, caused by an infection.... --CHILD--> [1D00.0] Bacterial encephalitis --- Walk 6 --- [1D00.Z] Infectious encephalitis, unspecified --PARENT--> [1D00] Infectious encephalitis, not elsewhere classified Def: A disease of the brain, caused by an infection.... --CHILD--> [1D00.2] Parasitic or protozoal encephalitis Def: A disease of the brain, caused by an infection with a parasitic or protozoal source....
[ "[8E7Y] Other specified diseases of the nervous system\n --PARENT--> [08] Diseases of the nervous system\n Def: This is a group of conditions characterised as being in or associated with the nervous system....\n --RELATED_TO--> [?] Syndromes with central nervous system anomalies as a major feature", "[8E7Y] Other specified diseases of the nervous system\n --PARENT--> [08] Diseases of the nervous system\n Def: This is a group of conditions characterised as being in or associated with the nervous system....\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 ...", "[LA05.Z] Cerebral structural developmental anomalies, unspecified\n --PARENT--> [LA05] Cerebral structural developmental anomalies\n Def: Any condition caused by failure of the brain to correctly develop during the antenatal period....\n --CHILD--> [LA05.1] Megalencephaly\n Def: A condition caused by failure of the brain to correctly develop during the antenatal period. This condition is characterised by increased size or weight of an otherwise correctly formed brain. This co...", "[LA05.Z] Cerebral structural developmental anomalies, unspecified\n --PARENT--> [LA05] Cerebral structural developmental anomalies\n Def: Any condition caused by failure of the brain to correctly develop during the antenatal period....\n --EXCLUDES--> [?] Encephalocele", "[1D00.Z] Infectious encephalitis, unspecified\n --PARENT--> [1D00] Infectious encephalitis, not elsewhere classified\n Def: A disease of the brain, caused by an infection....\n --CHILD--> [1D00.0] Bacterial encephalitis", "[1D00.Z] Infectious encephalitis, unspecified\n --PARENT--> [1D00] Infectious encephalitis, not elsewhere classified\n Def: A disease of the brain, caused by an infection....\n --CHILD--> [1D00.2] Parasitic or protozoal encephalitis\n Def: A disease of the brain, caused by an infection with a parasitic or protozoal source...." ]
8E7Y
Other specified diseases of the nervous system
[ { "from_icd11": "LA05.Z", "icd10_code": "Q048", "icd10_title": "Other specified congenital malformations of brain" }, { "from_icd11": "LA05.Z", "icd10_code": "Q043", "icd10_title": "Other reduction deformities of brain" }, { "from_icd11": "LA05.Z", "icd10_code": "Q049", "icd10_title": "Congenital malformation of brain, unspecified" }, { "from_icd11": "LA05.Z", "icd10_code": "Q04", "icd10_title": "Other congenital malformations of brain" }, { "from_icd11": "1D00.Z", "icd10_code": "G0490", "icd10_title": "Encephalitis and encephalomyelitis, unspecified" }, { "from_icd11": "1D00.Z", "icd10_code": "G0491", "icd10_title": "Myelitis, unspecified" }, { "from_icd11": "1D00.Z", "icd10_code": "G0430", "icd10_title": "Acute necrotizing hemorrhagic encephalopathy, unspecified" }, { "from_icd11": "1D00.Z", "icd10_code": "G0431", "icd10_title": "Postinfectious acute necrotizing hemorrhagic encephalopathy" }, { "from_icd11": "1D00.Z", "icd10_code": "G0439", "icd10_title": "Other acute necrotizing hemorrhagic encephalopathy" }, { "from_icd11": "1D00.Z", "icd10_code": "G0481", "icd10_title": "Other encephalitis and encephalomyelitis" }, { "from_icd11": "1D00.Z", "icd10_code": "G0489", "icd10_title": "Other myelitis" }, { "from_icd11": "1D00.Z", "icd10_code": "G04", "icd10_title": "Encephalitis, myelitis and encephalomyelitis" }, { "from_icd11": "1D00.Z", "icd10_code": "G048", "icd10_title": "Other encephalitis, myelitis and encephalomyelitis" }, { "from_icd11": "LA00.0Z", "icd10_code": "Q000", "icd10_title": "Anencephaly" }, { "from_icd11": "BE2Z", "icd10_code": "I998", "icd10_title": "Other disorder of circulatory system" } ]
Q048
Other specified congenital malformations of brain
Phlegmonous gastritis (PG) is a rare, severe infection of the gastric wall, with a high mortality rate of up to 40%. Pathophysiology is not fully understood, but it is thought to involve bacterial invasion of the gastric wall mucosa and reaching the muscular layer either directly or from bacteremia. These organisms may be gas-forming, and this leads to mucosal swelling, inflammation, and intramural gas . Clinical presentation is non-specific and may include severe epigastric abdominal pain, vomiting, and fever; however, purulent vomiting is characteristic . It is more common in patients with predisposing factors such as immunodeficiencies and alcoholism; however, it can happen in patients with no risk factors . A computed tomography (CT) scan can show diffuse thickening and edema of the gastric wall . Gastric endoscopy can show an inflamed gastric wall and occasionally purulent discharge and hemorrhage. Gastric biopsy is crucial for obtaining culture and ruling out gastric pathology . PG requires early, broad-spectrum antibiotics to reduce the mortality. Surgical intervention may be needed for possible complications like perforation and peritonitis . We report a patient who developed PG in the setting of the first presentation of acute leukemia, was successfully treated with systemic antimicrobial therapy and chemotherapy, and does not require total parenteral nutrition or surgical intervention.
4.199219
0.928711
sec[0]/p[0]
en
0.999997
40443637
https://doi.org/10.7759/cureus.83156
[ "gastric", "wall", "mortality", "vomiting", "however", "purulent", "patients", "factors", "intervention", "phlegmonous" ]
[ { "code": "DA4Z", "title": "Diseases of stomach, unspecified" }, { "code": "DA60.Z", "title": "Gastric ulcer, unspecified" }, { "code": "QF01.Y", "title": "Other specified acquired absence of organs" }, { "code": "LB13.Z", "title": "Structural developmental anomalies of stomach, unspecified" }, { "code": "DA42.73", "title": "Chronic atrophic gastritis of unknown aetiology" }, { "code": "LB0Y", "title": "Other specified structural developmental anomalies of the diaphragm, abdominal wall or umbilical cord" }, { "code": "PA82", "title": "Unintentional striking against stationary object" }, { "code": "NB50.Y&XA3KX0&XJ1C6", "title": "Haematoma of abdominal wall" }, { "code": "DC51.1", "title": "Peritoneal adhesions" }, { "code": "LB73.1Z", "title": "Structural developmental anomalies of chest wall, unspecified" } ]
=== ICD-11 CODES FOUND === [DA4Z] Diseases of stomach, unspecified Also known as: Diseases of stomach, unspecified | disorder of stomach | gastropathy NOS | gastric disease NOS | stomach disease NOS [DA60.Z] Gastric ulcer, unspecified Also known as: Gastric ulcer, unspecified | Gastric ulcer | stomach ulcer | Cushings ulcer | cushing's ulcer of stomach [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 [LB13.Z] Structural developmental anomalies of stomach, unspecified Also known as: Structural developmental anomalies of stomach, unspecified | Structural developmental anomalies of stomach | Malformations of stomach [DA42.73] Chronic atrophic gastritis of unknown aetiology Definition: Persistent or recurrent inflammation of the gastric mucosa with atrophy leading to decreased hydrochloric acid concentration in the gastric juice. Atrophic gastritis frequently progresses from chronic gastritis. Also known as: Chronic atrophic gastritis of unknown aetiology | Gastric atrophy | atrophic gastritis | AG - [atrophic gastritis] | CAG - [chronic atrophic gastritis] Includes: Gastric atrophy [LB0Y] Other specified structural developmental anomalies of the diaphragm, abdominal wall or umbilical cord Also known as: Other specified structural developmental anomalies of the diaphragm, abdominal wall or umbilical cord | Congenital deformity of abdominal wall | abdominal wall defect NOS [PA82] Unintentional striking against stationary object Also known as: Unintentional striking against stationary object | striking against stationary object | striking against or struck by other objects | Walked into wall [DC51.1] Peritoneal adhesions Definition: Disorders of peritoneum sticking by scar tissue or fibrosis Also known as: Peritoneal adhesions | abdominal adhesion | adhesive peritoneal band | peritoneal adhesion | peritoneal band Excludes: Adhesions of large intestine with obstruction | Postprocedural pelvic peritoneal adhesions | Intestinal adhesions or bands of small intestine with obstruction [LB73.1Z] Structural developmental anomalies of chest wall, unspecified Also known as: Structural developmental anomalies of chest wall, unspecified | Structural developmental anomalies of chest wall | Malformations of chest wall === GRAPH WALKS === --- Walk 1 --- [DA4Z] Diseases of stomach, unspecified --PARENT--> [?] Diseases of stomach Def: This is a group of conditions characterised as being in or associated with the stomach.... --EXCLUDES--> [?] Gastrostomy malfunction --- Walk 2 --- [DA4Z] Diseases of stomach, unspecified --PARENT--> [?] Diseases of stomach Def: This is a group of conditions characterised as being in or associated with the stomach.... --RELATED_TO--> [?] Gastric ulcer Def: Gastric ulcer is defined as a distinct breach in the mucosa of the stomach as a result of caustic effects of acid and pepsin in the lumen. Histologically, gastric ulcer is identified as necrosis of th... --- Walk 3 --- [DA60.Z] Gastric ulcer, unspecified --PARENT--> [DA60] Gastric ulcer Def: Gastric ulcer is defined as a distinct breach in the mucosa of the stomach as a result of caustic effects of acid and pepsin in the lumen. Histologically, gastric ulcer is identified as necrosis of th... --CHILD--> [DA60.1] Helicobacter pylori associated gastric ulcer Def: Helicobacter pylori (H. pylori) is a gram-negative bacillus that is found in the mucous layer overlying gastric epithelium, within epithelial cells and attached to mucous cells, leading to inflammatio... --- Walk 4 --- [DA60.Z] Gastric ulcer, unspecified --PARENT--> [DA60] Gastric ulcer Def: Gastric ulcer is defined as a distinct breach in the mucosa of the stomach as a result of caustic effects of acid and pepsin in the lumen. Histologically, gastric ulcer is identified as necrosis of th... --EXCLUDES--> [?] Acute haemorrhagic gastritis of unknown aetiology Def: Rapid onset inflammation of the mucosal lining of the stomach with associated bleeding or abnormal blood flow.... --- Walk 5 --- [QF01.Y] Other specified acquired absence of organs --PARENT--> [QF01] Acquired absence of organs --PARENT--> [?] Acquired absence of body structure --- Walk 6 --- [QF01.Y] Other specified acquired absence of organs --PARENT--> [QF01] Acquired absence of organs --EXCLUDES--> [?] Postprocedural endocrine or metabolic disorders Def: Any endocrine or metabolic disorder caused by or subsequent to any medical procedure....
[ "[DA4Z] Diseases of stomach, unspecified\n --PARENT--> [?] Diseases of stomach\n Def: This is a group of conditions characterised as being in or associated with the stomach....\n --EXCLUDES--> [?] Gastrostomy malfunction", "[DA4Z] Diseases of stomach, unspecified\n --PARENT--> [?] Diseases of stomach\n Def: This is a group of conditions characterised as being in or associated with the stomach....\n --RELATED_TO--> [?] Gastric ulcer\n Def: Gastric ulcer is defined as a distinct breach in the mucosa of the stomach as a result of caustic effects of acid and pepsin in the lumen. Histologically, gastric ulcer is identified as necrosis of th...", "[DA60.Z] Gastric ulcer, unspecified\n --PARENT--> [DA60] Gastric ulcer\n Def: Gastric ulcer is defined as a distinct breach in the mucosa of the stomach as a result of caustic effects of acid and pepsin in the lumen. Histologically, gastric ulcer is identified as necrosis of th...\n --CHILD--> [DA60.1] Helicobacter pylori associated gastric ulcer\n Def: Helicobacter pylori (H. pylori) is a gram-negative bacillus that is found in the mucous layer overlying gastric epithelium, within epithelial cells and attached to mucous cells, leading to inflammatio...", "[DA60.Z] Gastric ulcer, unspecified\n --PARENT--> [DA60] Gastric ulcer\n Def: Gastric ulcer is defined as a distinct breach in the mucosa of the stomach as a result of caustic effects of acid and pepsin in the lumen. Histologically, gastric ulcer is identified as necrosis of th...\n --EXCLUDES--> [?] Acute haemorrhagic gastritis of unknown aetiology\n Def: Rapid onset inflammation of the mucosal lining of the stomach with associated bleeding or abnormal blood flow....", "[QF01.Y] Other specified acquired absence of organs\n --PARENT--> [QF01] Acquired absence of organs\n --PARENT--> [?] Acquired absence of body structure", "[QF01.Y] Other specified acquired absence of organs\n --PARENT--> [QF01] Acquired absence of organs\n --EXCLUDES--> [?] Postprocedural endocrine or metabolic disorders\n Def: Any endocrine or metabolic disorder caused by or subsequent to any medical procedure...." ]
DA4Z
Diseases of stomach, unspecified
[ { "from_icd11": "DA60.Z", "icd10_code": "K259", "icd10_title": "Gastric ulcer, unspecified as acute or chronic, without hemorrhage or perforation" }, { "from_icd11": "DA60.Z", "icd10_code": "K255", "icd10_title": "Chronic or unspecified gastric ulcer with perforation" }, { "from_icd11": "DA60.Z", "icd10_code": "K254", "icd10_title": "Chronic or unspecified gastric ulcer with hemorrhage" }, { "from_icd11": "DA60.Z", "icd10_code": "K257", "icd10_title": "Chronic gastric ulcer without hemorrhage or perforation" }, { "from_icd11": "DA60.Z", "icd10_code": "K250", "icd10_title": "Acute gastric ulcer with hemorrhage" }, { "from_icd11": "DA60.Z", "icd10_code": "K256", "icd10_title": "Chronic or unspecified gastric ulcer with both hemorrhage and perforation" }, { "from_icd11": "DA60.Z", "icd10_code": "K253", "icd10_title": "Acute gastric ulcer without hemorrhage or perforation" }, { "from_icd11": "DA60.Z", "icd10_code": "K252", "icd10_title": "Acute gastric ulcer with both hemorrhage and perforation" }, { "from_icd11": "DA60.Z", "icd10_code": "K251", "icd10_title": "Acute gastric ulcer with perforation" }, { "from_icd11": "DA60.Z", "icd10_code": "K25", "icd10_title": "Gastric ulcer" }, { "from_icd11": "QF01.Y", "icd10_code": "Z9049", "icd10_title": "Acquired absence of other specified parts of digestive tract" }, { "from_icd11": "LB13.Z", "icd10_code": "Q402", "icd10_title": "Other specified congenital malformations of stomach" }, { "from_icd11": "LB13.Z", "icd10_code": "Q403", "icd10_title": "Congenital malformation of stomach, unspecified" }, { "from_icd11": "DA42.73", "icd10_code": "K2940", "icd10_title": "Chronic atrophic gastritis without bleeding" }, { "from_icd11": "DA42.73", "icd10_code": "K2941", "icd10_title": "Chronic atrophic gastritis with bleeding" } ]
K259
Gastric ulcer, unspecified as acute or chronic, without hemorrhage or perforation
A 45-year-old male patient presented with a history of elephantiasis in the right lower limb, spanning over five years, with no prior treatment. Three days prior to presentation, the patient sustained a fall from a bicycle, resulting in trauma to his right foot. Subsequently, he noted an increase in redness and swelling of the affected foot, which was insidious in onset and progressively worsened. Concurrently, he developed respiratory distress, increased drowsiness, and lethargy, and experienced a persistent low-grade fever two days earlier. Initially, the patient was treated at an external medical facility, where he underwent local debridement of the affected site on July 13, 2023. Due to the exacerbation of symptoms, including increased drowsiness and hypotension, along with plans for plastic surgery, he was then referred to our institution for further management. The patient does not have any systemic diseases or illnesses. Notable findings upon examination included a wound measuring approximately 10x6 cm on the lateral aspect of the right lower limb, 5x4 cm on the foot, and 10x7 cm on the medial aspect. Local examination showed that slough was present, indicating tissue necrosis, along with tenderness, while redness was notably absent. Non-pitting edema was also present. A surgical consultation confirmed the diagnosis of cellulitis in the right lower limb, necessitating debridement surgery.
3.757813
0.985352
sec[1]/p[0]
en
0.999997
PMC11364152
https://doi.org/10.7759/cureus.65855
[ "limb", "foot", "redness", "affected", "drowsiness", "local", "debridement", "along", "aspect", "present" ]
[ { "code": "ND56.1", "title": "Open wound of unspecified body region" }, { "code": "LB9Z", "title": "Structural developmental anomalies of the skeleton, unspecified" }, { "code": "FB56.6", "title": "Other specified soft tissue disorders" }, { "code": "5B51&XS25", "title": "Severe wasting in infants, children or adolescents" }, { "code": "ND55", "title": "Other injuries of leg, level unspecified" }, { "code": "ND19.Z", "title": "Traumatic amputation of ankle or foot, unspecified" }, { "code": "QF00", "title": "Acquired absence of limb" }, { "code": "ND14.A", "title": "Strain or sprain of other or unspecified parts of foot" }, { "code": "ND11.Y", "title": "Other specified superficial injury of ankle or foot" }, { "code": "LB9A.6", "title": "Split foot" } ]
=== ICD-11 CODES FOUND === [ND56.1] Open wound of unspecified body region Also known as: Open wound of unspecified body region | cut NOS | open wound NOS | penetrating wound NOS | Puncture wound with foreign body unspecified body region Excludes: Traumatic amputations involving multiple body regions | Open wounds involving multiple body regions | traumatic amputation NOS [LB9Z] Structural developmental anomalies of the skeleton, unspecified Also known as: Structural developmental anomalies of the skeleton, unspecified | Abnormal bone development | skeletal anomaly NOS [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 [ND55] Other injuries of leg, level unspecified Also known as: Other injuries of leg, level unspecified | other injuries of lower limb, level unspecified | Superficial injury of leg, level unspecified | Abrasion of leg, level unspecified | Contusion of leg, level unspecified Excludes: Fracture of leg, level unspecified | Injuries involving multiple body regions [ND19.Z] Traumatic amputation of ankle or foot, unspecified Also known as: Traumatic amputation of ankle or foot, unspecified | Traumatic amputation of ankle or foot | traumatic amputation of foot | avulsion of foot | severed foot [QF00] Acquired absence of limb Also known as: Acquired absence of limb | post traumatic loss of limb | postoperative loss of limb | bilateral amputee | amputee Includes: postoperative loss of limb | post traumatic loss of limb Excludes: Other acquired deformities of limbs | Congenital absence of thigh or lower leg with foot present | Congenital absence of both lower leg and foot [ND14.A] Strain or sprain of other or unspecified parts of foot Also known as: Strain or sprain of other or unspecified parts of foot | Sprain of foot | Strain of foot | Midtarsal sprain | Midtarsal strain [ND11.Y] Other specified superficial injury of ankle or foot Also known as: Other specified superficial injury of ankle or foot | Contusion of toe with damage to nail | Haematoma of foot | feet haematoma | Nonthermal blister of toe [LB9A.6] Split foot Definition: A condition caused by malformation of the foot during the antenatal period. This condition is characterised by a deep median cleft of the foot due to the absence of the central rays. Also known as: Split foot | lobster claw foot | split foot, unspecified side | cleft of foot | Split foot, unilateral === GRAPH WALKS === --- Walk 1 --- [ND56.1] Open wound of unspecified body region --EXCLUDES--> [?] Traumatic amputations involving multiple body regions --EXCLUDES--> [?] Open wounds involving multiple body regions --- Walk 2 --- [ND56.1] Open wound of unspecified body region --EXCLUDES--> [?] Traumatic amputations involving multiple body regions --CHILD--> [?] Traumatic amputation of both hands --- Walk 3 --- [LB9Z] Structural developmental anomalies of the skeleton, unspecified --PARENT--> [?] Structural developmental anomalies of the skeleton Def: A deformation established before birth of an anatomical structure of one or more bones.... --CHILD--> [LB70] Structural developmental anomalies of cranium Def: Any condition caused by failure of the cranium to correctly develop during the antenatal period.... --- Walk 4 --- [LB9Z] Structural developmental anomalies of the skeleton, unspecified --PARENT--> [?] Structural developmental anomalies of the skeleton Def: A deformation established before birth of an anatomical structure of one or more bones.... --CHILD--> [LB72] Structural developmental anomalies of shoulder girdle Def: Any condition caused by failure of the shoulder girdle to correctly develop during the antenatal period.... --- Walk 5 --- [FB56.6] Other specified soft tissue disorders --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--> [?] Radiculopathy --- Walk 6 --- [FB56.6] Other specified soft tissue disorders --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.... --CHILD--> [FB56.0] Foreign body granuloma of soft tissue, not elsewhere classified
[ "[ND56.1] Open wound of unspecified body region\n --EXCLUDES--> [?] Traumatic amputations involving multiple body regions\n --EXCLUDES--> [?] Open wounds involving multiple body regions", "[ND56.1] Open wound of unspecified body region\n --EXCLUDES--> [?] Traumatic amputations involving multiple body regions\n --CHILD--> [?] Traumatic amputation of both hands", "[LB9Z] Structural developmental anomalies of the skeleton, unspecified\n --PARENT--> [?] Structural developmental anomalies of the skeleton\n Def: A deformation established before birth of an anatomical structure of one or more bones....\n --CHILD--> [LB70] Structural developmental anomalies of cranium\n Def: Any condition caused by failure of the cranium to correctly develop during the antenatal period....", "[LB9Z] Structural developmental anomalies of the skeleton, unspecified\n --PARENT--> [?] Structural developmental anomalies of the skeleton\n Def: A deformation established before birth of an anatomical structure of one or more bones....\n --CHILD--> [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....", "[FB56.6] Other specified soft tissue disorders\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--> [?] Radiculopathy", "[FB56.6] Other specified soft tissue disorders\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 --CHILD--> [FB56.0] Foreign body granuloma of soft tissue, not elsewhere classified" ]
ND56.1
Open wound of unspecified body region
[ { "from_icd11": "ND56.1", "icd10_code": "T141", "icd10_title": "" }, { "from_icd11": "LB9Z", "icd10_code": "Q8789", "icd10_title": "Other specified congenital malformation syndromes, not elsewhere classified" }, { "from_icd11": "LB9Z", "icd10_code": "Q8781", "icd10_title": "Alport syndrome" }, { "from_icd11": "LB9Z", "icd10_code": "Q742", "icd10_title": "Other congenital malformations of lower limb(s), including pelvic girdle" }, { "from_icd11": "LB9Z", "icd10_code": "Q749", "icd10_title": "Unspecified congenital malformation of limb(s)" }, { "from_icd11": "LB9Z", "icd10_code": "Q740", "icd10_title": "Other congenital malformations of upper limb(s), including shoulder girdle" }, { "from_icd11": "LB9Z", "icd10_code": "Q741", "icd10_title": "Congenital malformation of knee" }, { "from_icd11": "LB9Z", "icd10_code": "Q875", "icd10_title": "Other congenital malformation syndromes with other skeletal changes" }, { "from_icd11": "LB9Z", "icd10_code": "Q748", "icd10_title": "Other specified congenital malformations of limb(s)" }, { "from_icd11": "LB9Z", "icd10_code": "Q89", "icd10_title": "Other congenital malformations, not elsewhere classified" }, { "from_icd11": "LB9Z", "icd10_code": "Q65-Q79", "icd10_title": "" }, { "from_icd11": "LB9Z", "icd10_code": "Q73", "icd10_title": "Reduction defects of unspecified limb" }, { "from_icd11": "LB9Z", "icd10_code": "Q730", "icd10_title": "Congenital absence of unspecified limb(s)" }, { "from_icd11": "LB9Z", "icd10_code": "Q731", "icd10_title": "Phocomelia, unspecified limb(s)" }, { "from_icd11": "LB9Z", "icd10_code": "Q74", "icd10_title": "Other congenital malformations of limb(s)" } ]
T141
After two weeks of gradual clinical improvement, the patient experienced acute-on-chronic neurological deterioration with further decreased consciousness, hemispatial neglect, increased upper limb tone, and reduced lower limb reflexes. An urgent CT brain scan showed early hydrocephalus. Subsequent cranial MRI showed diffusion-restricting fluid-fluid levels in the lateral ventricles, which were initially interpreted as intraventricular haemorrhage. CT angiography showed no vascular abnormality or bleeding point. A follow-up cranial MRI with contrast revealed linear ependymal enhancement in the occipital horns and leptomeningeal enhancement without evidence of bleeding, findings that were consistent with pyogenic ventriculitis . A diagnostic lumbar puncture confirmed bacterial meningitis (Table 2 ). At this stage, meropenem was used for ESBL E. coli pyelitis/emphysematous cystitis with linezolid, fluconazole, ciprofloxacin, and ivermectin for SHS due to concurrent vancomycin-resistant Enterococcus (VRE) and candiduria. E . raffinosus was cultured from the cerebrospinal fluid (CSF) resistant to penicillin and ampicillin but sensitive to vancomycin and ciprofloxacin (Vanc MIC <16 on Vitek, CLSI (Clinical and Laboratory Standards Institute)). Bacterial DNA was confirmed by 16S PCR/NAAT. CSF analysis by wet mount was negative for parasites or filariform larvae. He tested negative for HIV and HTLV-1/2.
4.097656
0.967773
sec[1]/p[3]
en
0.999998
40385832
https://doi.org/10.7759/cureus.82417
[ "fluid", "limb", "bleeding", "enhancement", "bacterial", "ciprofloxacin", "vancomycin", "resistant", "gradual", "improvement" ]
[ { "code": "FA36.Z", "title": "Effusion of joint, unspecified" }, { "code": "5C70.0", "title": "Dehydration" }, { "code": "5C78", "title": "Fluid overload" }, { "code": "MG29.Z", "title": "Oedema, unspecified" }, { "code": "ME04.Z", "title": "Ascites, unspecified" }, { "code": "ND56.1", "title": "Open wound of unspecified body region" }, { "code": "LB9Z", "title": "Structural developmental anomalies of the skeleton, unspecified" }, { "code": "FB56.6", "title": "Other specified soft tissue disorders" }, { "code": "5B51&XS25", "title": "Severe wasting in infants, children or adolescents" }, { "code": "ND55", "title": "Other injuries of leg, level unspecified" } ]
=== ICD-11 CODES FOUND === [FA36.Z] Effusion of joint, unspecified Also known as: Effusion of joint, unspecified | Effusion of joint | effusion into joint | effusion of joint, site unspecified | hydrarthrosis [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 [5C78] Fluid overload Definition: This is the condition where there is too much fluid in the blood. The opposite condition is hypovolemia, which is too little fluid volume in the blood. Fluid volume excess in the intravascular compartment occurs due to an increase in total body sodium content and a consequent increase in extracellular body water. The mechanism usually stems from compromised regulatory mechanisms for sodium handling as seen in congestive heart failure (CHF), kidney failure, and liver failure. It may also be cause Also known as: Fluid overload | fluid excess | fluid volume excess | hypervolemia | volume excess [MG29.Z] Oedema, unspecified Also known as: Oedema, unspecified | Oedema | dropsy | hydrops | Fluid retention NOS [ME04.Z] Ascites, unspecified Also known as: Ascites, unspecified | Ascites | abdominal dropsy | hydrops abdominis | ascites NOS [ND56.1] Open wound of unspecified body region Also known as: Open wound of unspecified body region | cut NOS | open wound NOS | penetrating wound NOS | Puncture wound with foreign body unspecified body region Excludes: Traumatic amputations involving multiple body regions | Open wounds involving multiple body regions | traumatic amputation NOS [LB9Z] Structural developmental anomalies of the skeleton, unspecified Also known as: Structural developmental anomalies of the skeleton, unspecified | Abnormal bone development | skeletal anomaly NOS [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 [ND55] Other injuries of leg, level unspecified Also known as: Other injuries of leg, level unspecified | other injuries of lower limb, level unspecified | Superficial injury of leg, level unspecified | Abrasion of leg, level unspecified | Contusion of leg, level unspecified Excludes: Fracture of leg, level unspecified | Injuries involving multiple body regions === GRAPH WALKS === --- Walk 1 --- [FA36.Z] Effusion of joint, unspecified --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.Y] Other specified effusion of joint --- Walk 2 --- [FA36.Z] Effusion of joint, unspecified --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.Z] Effusion of joint, unspecified --- Walk 3 --- [5C70.0] Dehydration Def: 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... --RELATED_TO--> [?] Dehydration of newborn Def: A paediatric condition characterised by excessive loss of body water in a newborn.... --PARENT--> [?] Certain specified transitory neonatal electrolyte or metabolic disturbances Def: A group of paediatric conditions in which there is a temporary abnormality in the normal processes of enzyme catalyzed reactions within tissue cells (metabolism) or with the levels of minerals in the ... --- Walk 4 --- [5C70.0] Dehydration Def: 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... --RELATED_TO--> [?] Dehydration of newborn Def: A paediatric condition characterised by excessive loss of body water in a newborn.... --PARENT--> [?] Certain specified transitory neonatal electrolyte or metabolic disturbances Def: A group of paediatric conditions in which there is a temporary abnormality in the normal processes of enzyme catalyzed reactions within tissue cells (metabolism) or with the levels of minerals in the ... --- Walk 5 --- [5C78] Fluid overload Def: This is the condition where there is too much fluid in the blood. The opposite condition is hypovolemia, which is too little fluid volume in the blood. Fluid volume excess in the intravascular compart... --PARENT--> [?] Disorders of fluid, electrolyte or acid-base balance --CHILD--> [5C70] Volume depletion --- Walk 6 --- [5C78] Fluid overload Def: This is the condition where there is too much fluid in the blood. The opposite condition is hypovolemia, which is too little fluid volume in the blood. Fluid volume excess in the intravascular compart... --PARENT--> [?] Disorders of fluid, electrolyte or acid-base balance --CHILD--> [5C72] Hypo-osmolality or hyponatraemia Def: Serum sodium concentrations of less than 135 mEq/L; decreased serum concentration of osmotically active particles...
[ "[FA36.Z] Effusion of joint, unspecified\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.Y] Other specified effusion of joint", "[FA36.Z] Effusion of joint, unspecified\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.Z] Effusion of joint, unspecified", "[5C70.0] Dehydration\n Def: 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...\n --RELATED_TO--> [?] Dehydration of newborn\n Def: A paediatric condition characterised by excessive loss of body water in a newborn....\n --PARENT--> [?] Certain specified transitory neonatal electrolyte or metabolic disturbances\n Def: A group of paediatric conditions in which there is a temporary abnormality in the normal processes of enzyme catalyzed reactions within tissue cells (metabolism) or with the levels of minerals in the ...", "[5C70.0] Dehydration\n Def: 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...\n --RELATED_TO--> [?] Dehydration of newborn\n Def: A paediatric condition characterised by excessive loss of body water in a newborn....\n --PARENT--> [?] Certain specified transitory neonatal electrolyte or metabolic disturbances\n Def: A group of paediatric conditions in which there is a temporary abnormality in the normal processes of enzyme catalyzed reactions within tissue cells (metabolism) or with the levels of minerals in the ...", "[5C78] Fluid overload\n Def: This is the condition where there is too much fluid in the blood. The opposite condition is hypovolemia, which is too little fluid volume in the blood. Fluid volume excess in the intravascular compart...\n --PARENT--> [?] Disorders of fluid, electrolyte or acid-base balance\n --CHILD--> [5C70] Volume depletion", "[5C78] Fluid overload\n Def: This is the condition where there is too much fluid in the blood. The opposite condition is hypovolemia, which is too little fluid volume in the blood. Fluid volume excess in the intravascular compart...\n --PARENT--> [?] Disorders of fluid, electrolyte or acid-base balance\n --CHILD--> [5C72] Hypo-osmolality or hyponatraemia\n Def: Serum sodium concentrations of less than 135 mEq/L; decreased serum concentration of osmotically active particles..." ]
FA36.Z
Effusion of joint, unspecified
[ { "from_icd11": "FA36.Z", "icd10_code": "M25471", "icd10_title": "Effusion, right ankle" }, { "from_icd11": "FA36.Z", "icd10_code": "M25461", "icd10_title": "Effusion, right knee" }, { "from_icd11": "FA36.Z", "icd10_code": "M25462", "icd10_title": "Effusion, left knee" }, { "from_icd11": "FA36.Z", "icd10_code": "M25431", "icd10_title": "Effusion, right wrist" }, { "from_icd11": "FA36.Z", "icd10_code": "M25472", "icd10_title": "Effusion, left ankle" }, { "from_icd11": "FA36.Z", "icd10_code": "M25451", "icd10_title": "Effusion, right hip" }, { "from_icd11": "FA36.Z", "icd10_code": "M2548", "icd10_title": "Effusion, other site" }, { "from_icd11": "FA36.Z", "icd10_code": "M25411", "icd10_title": "Effusion, right shoulder" }, { "from_icd11": "FA36.Z", "icd10_code": "M25441", "icd10_title": "Effusion, right hand" }, { "from_icd11": "FA36.Z", "icd10_code": "M25452", "icd10_title": "Effusion, left hip" }, { "from_icd11": "FA36.Z", "icd10_code": "M25421", "icd10_title": "Effusion, right elbow" }, { "from_icd11": "FA36.Z", "icd10_code": "M25432", "icd10_title": "Effusion, left wrist" }, { "from_icd11": "FA36.Z", "icd10_code": "M25473", "icd10_title": "Effusion, unspecified ankle" }, { "from_icd11": "FA36.Z", "icd10_code": "M25412", "icd10_title": "Effusion, left shoulder" }, { "from_icd11": "FA36.Z", "icd10_code": "M25422", "icd10_title": "Effusion, left elbow" } ]
M25471
Effusion, right ankle
In patients with ILC, treatment involves a combination of surgery, chemotherapy, and radiation therapy. Prior to initiation of treatment, a preoperative MR is often obtained to verify the extent of the cancer and to inform the best treatment approach. Surgical excision with clear margins may be performed, however, due to the diffuse nature of ILC, mastectomy is considered especially in cases of multifocal or multicentric disease. Postoperatively, radiation therapy is administered for extensive disease. Neoadjuvant chemoradiation is considered in patients with tumors with advanced stage . Selection of hormonal agents is guided by ER/PR/HER2 status. In patients with ER/PR-positive tumors, tamoxifen is utilized for premenopausal women, while an aromatase inhibitor is preferred in postmenopausal women . In HER2 positive tumors, trastuzumab is the drug of choice . In cases involving pectoralis muscle invasion, excision of the muscle is performed along with the appropriate surgical and systemic therapies. Ultimately a multidisciplinary approach involving surgeons, oncologists, and radiation therapists is essential to formulate an effective treatment regimen tailored to a patient's clinical situation. Our patient was treated with mastectomy, endocrine therapy utilizing letrozole, an aromatase inhibitor, and adjuvant chemotherapy consisting of doxorubicin and cyclophosphamide with pegfilgrastim support.
4.234375
0.599121
sec[2]/p[3]
en
0.999998
40242378
https://doi.org/10.1016/j.radcr.2025.03.051
[ "patients", "radiation", "tumors", "chemotherapy", "approach", "excision", "mastectomy", "considered", "cases", "women" ]
[ { "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": "NF00", "title": "Effects of radiation, not elsewhere classified" }, { "code": "QC48.Y", "title": "Other specified personal history of medical treatment" }, { "code": "EK90.Y", "title": "Other discrete epidermal dysplasias" }, { "code": "CA82.1", "title": "Chronic or other pulmonary manifestations due to radiation" }, { "code": "DA25.32", "title": "Radiation oesophageal ulcer" } ]
=== 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 [NF00] Effects of radiation, not elsewhere classified Also known as: Effects of radiation, not elsewhere classified | radiation complications | infrared rays injury | Radiation sickness Excludes: Sunburn | Burns | specified adverse effects of radiation, such as leukaemia [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 [EK90.Y] Other discrete epidermal dysplasias Also known as: Other discrete epidermal dysplasias | Actinic cheilitis | Photochemotherapy-induced keratosis | Thermal keratosis | Chronic radiation keratosis [CA82.1] Chronic or other pulmonary manifestations due to radiation Definition: A chronic inflammatory reaction of the lung ultimately resulting in fibrosis in response to repeated or high dose radiation exposure. Also known as: Chronic or other pulmonary manifestations due to radiation | Fibrosis of lung following radiation | radiation fibrosis of lung | Chronic radiation pulmonary fibrosis [DA25.32] Radiation oesophageal ulcer Also known as: Radiation oesophageal ulcer === 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 --PARENT--> [?] Mode of injury or harm associated with a surgical or other medical procedure --- 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 --EXCLUDES--> [?] Patient received diagnostic test or treatment intended for another patient --- Walk 3 --- [QB14] Unavailability or inaccessibility of health care facilities --PARENT--> [?] Factors related to medical facilities or other health care --CHILD--> [QB10] Medical services not available in home --- Walk 4 --- [QB14] Unavailability or inaccessibility of health care facilities --PARENT--> [?] Factors related to medical facilities or other health care --CHILD--> [QB10] Medical services not available in home --- 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 --CHILD--> [PL14.2] Problem associated with physical transfer of patient --- 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 --CHILD--> [PL14.0] Non-administration of necessary drug
[ "[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", "[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 --EXCLUDES--> [?] Patient received diagnostic test or treatment intended for another patient", "[QB14] Unavailability or inaccessibility of health care facilities\n --PARENT--> [?] Factors related to medical facilities or other health care\n --CHILD--> [QB10] Medical services not available in home", "[QB14] Unavailability or inaccessibility of health care facilities\n --PARENT--> [?] Factors related to medical facilities or other health care\n --CHILD--> [QB10] Medical services not available in home", "[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 --CHILD--> [PL14.2] Problem associated with physical transfer of patient", "[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 --CHILD--> [PL14.0] Non-administration of necessary drug" ]
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": "NF00", "icd10_code": "T66XXXA", "icd10_title": "Radiation sickness, unspecified, initial encounter" }, { "from_icd11": "NF00", "icd10_code": "T66XXXS", "icd10_title": "Radiation sickness, unspecified, sequela" }, { "from_icd11": "NF00", "icd10_code": "T66", "icd10_title": "Radiation sickness, unspecified" }, { "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" } ]
Z753
Unavailability and inaccessibility of health-care facilities
Laboratory investigations showed normocytic anemia and marked eosinophilia. Peripheral blood smear analysis confirmed normocytic normochromic erythrocytes, mild anisopoikilocytosis, and an elevated eosinophil count with normal leukocyte and platelet morphology. Liver function tests were within normal limits. Abdominal ultrasonography revealed moderate ascites with no discernible organomegaly. Given the significant eosinophilia, absolute eosinophil count (AEC) and serum immunoglobulin E (IgE) levels were measured, showing elevated levels of 3470 IU/mL and 971 cells/µL, respectively (Table 1 ). The analysis of the ascitic fluid confirmed eosinophilic ascites and showed a low serum-ascites albumin gradient (SAAG) along with high protein levels (Table 2 ). Serial stool cultures, sensitivity tests, and routine stool examinations for ova and cysts were performed but returned negative results. In light of the patient’s occupation and clinical findings, including eosinophilic ascites, differential diagnoses included parasitic infections such as filariasis or strongyloidiasis. Serological testing for filariasis and a duodenal biopsy for strongyloidiasis were performed, both of which returned negative results. However, the patient was treated empirically with diethylcarbamazine and ivermectin for two weeks, targeting potential parasitic etiologies, without symptomatic improvement or resolution of ascites.
4.171875
0.921875
sec[1]/p[2]
en
0.999996
39364509
https://doi.org/10.7759/cureus.68511
[ "ascites", "normocytic", "eosinophilia", "eosinophil", "count", "serum", "eosinophilic", "stool", "returned", "parasitic" ]
[ { "code": "ME04.Z", "title": "Ascites, unspecified" }, { "code": "ME04.Y", "title": "Other specified ascites" }, { "code": "DC51.0", "title": "Chylous ascites" }, { "code": "2D91", "title": "Malignant neoplasm metastasis in peritoneum" }, { "code": "1B12.7", "title": "Tuberculosis of the digestive system" }, { "code": "4B03.Z", "title": "Eosinophilia, unspecified" }, { "code": "4B03.0", "title": "Constitutional eosinophilia" }, { "code": "4B03.1", "title": "Acquired eosinophilia" }, { "code": "CB02.Z", "title": "Pulmonary eosinophilia, unspecified" }, { "code": "CB02.Y", "title": "Other specified pulmonary eosinophilia" } ]
=== ICD-11 CODES FOUND === [ME04.Z] Ascites, unspecified Also known as: Ascites, unspecified | Ascites | abdominal dropsy | hydrops abdominis | ascites NOS [ME04.Y] Other specified ascites Also known as: Other specified ascites [DC51.0] Chylous ascites Definition: Chylous ascites is a rare form of ascites caused by accumulation of lymph in the peritoneal cavity, usually due to intra-abdominal malignancy, liver cirrhosis or abdominal surgery complications, and present with painless but progressive abdominal distension, dyspnoea and weight gain. Also known as: Chylous ascites | chyloperitoneum [2D91] Malignant neoplasm metastasis in peritoneum Also known as: Malignant neoplasm metastasis in peritoneum | peritoneal metastases | peritoneal metastasis | carcinomatosis of peritoneal cavity | carcinomatosis peritonei [1B12.7] Tuberculosis of the digestive system Definition: Tuberculosis of the digestive tract or hepatobiliary system Also known as: Tuberculosis of the digestive system | tuberculosis of gastrointestinal tract | Tuberculous duodenitis | Tuberculous gastritis | tuberculosis of stomach [4B03.Z] Eosinophilia, unspecified Also known as: Eosinophilia, unspecified | Eosinophilia | Disorders with increased eosinophil counts | Idiopathic hypereosinophilic syndrome [4B03.0] Constitutional eosinophilia Also known as: Constitutional eosinophilia | Congenital eosinophilia [4B03.1] Acquired eosinophilia Also known as: Acquired eosinophilia | Infection-related eosinophilia | Eosinophilia due to allergic diseases | Eosinophilia due to drug reaction | Eosinophilia reactive to neoplasm [CB02.Z] Pulmonary eosinophilia, unspecified Also known as: Pulmonary eosinophilia, unspecified | Pulmonary eosinophilia | eosinophilic lung infiltrate | Weingarten's syndrome [CB02.Y] Other specified pulmonary eosinophilia Also known as: Other specified pulmonary eosinophilia === GRAPH WALKS === --- Walk 1 --- [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 2 --- [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 3 --- [ME04.Y] Other specified ascites --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 4 --- [ME04.Y] Other specified ascites --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 --- Walk 5 --- [DC51.0] Chylous ascites Def: Chylous ascites is a rare form of ascites caused by accumulation of lymph in the peritoneal cavity, usually due to intra-abdominal malignancy, liver cirrhosis or abdominal surgery complications, and p... --PARENT--> [DC51] Certain specified disorders of peritoneum or retroperitoneum --CHILD--> [DC51.0] Chylous ascites Def: Chylous ascites is a rare form of ascites caused by accumulation of lymph in the peritoneal cavity, usually due to intra-abdominal malignancy, liver cirrhosis or abdominal surgery complications, and p... --- Walk 6 --- [DC51.0] Chylous ascites Def: Chylous ascites is a rare form of ascites caused by accumulation of lymph in the peritoneal cavity, usually due to intra-abdominal malignancy, liver cirrhosis or abdominal surgery complications, and p... --PARENT--> [DC51] Certain specified disorders of peritoneum or retroperitoneum --EXCLUDES--> [?] 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...
[ "[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--> [ME04.0] Fluid in peritoneal cavity", "[ME04.Y] Other specified ascites\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.Y] Other specified ascites\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", "[DC51.0] Chylous ascites\n Def: Chylous ascites is a rare form of ascites caused by accumulation of lymph in the peritoneal cavity, usually due to intra-abdominal malignancy, liver cirrhosis or abdominal surgery complications, and p...\n --PARENT--> [DC51] Certain specified disorders of peritoneum or retroperitoneum\n --CHILD--> [DC51.0] Chylous ascites\n Def: Chylous ascites is a rare form of ascites caused by accumulation of lymph in the peritoneal cavity, usually due to intra-abdominal malignancy, liver cirrhosis or abdominal surgery complications, and p...", "[DC51.0] Chylous ascites\n Def: Chylous ascites is a rare form of ascites caused by accumulation of lymph in the peritoneal cavity, usually due to intra-abdominal malignancy, liver cirrhosis or abdominal surgery complications, and p...\n --PARENT--> [DC51] Certain specified disorders of peritoneum or retroperitoneum\n --EXCLUDES--> [?] 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..." ]
ME04.Z
Ascites, unspecified
[ { "from_icd11": "ME04.Z", "icd10_code": "R180", "icd10_title": "Malignant ascites" }, { "from_icd11": "ME04.Z", "icd10_code": "R18", "icd10_title": "Ascites" }, { "from_icd11": "ME04.Y", "icd10_code": "R188", "icd10_title": "Other ascites" }, { "from_icd11": "1B12.7", "icd10_code": "A1883", "icd10_title": "Tuberculosis of digestive tract organs, not elsewhere classified" }, { "from_icd11": "1B12.7", "icd10_code": "A1832", "icd10_title": "Tuberculous enteritis" }, { "from_icd11": "1B12.7", "icd10_code": "A1884", "icd10_title": "Tuberculosis of heart" }, { "from_icd11": "1B12.7", "icd10_code": "A1889", "icd10_title": "Tuberculosis of other sites" }, { "from_icd11": "1B12.7", "icd10_code": "A1839", "icd10_title": "Retroperitoneal tuberculosis" }, { "from_icd11": "1B12.7", "icd10_code": "A1831", "icd10_title": "Tuberculous peritonitis" }, { "from_icd11": "1B12.7", "icd10_code": "K67", "icd10_title": "Disorders of peritoneum in infectious diseases classified elsewhere" }, { "from_icd11": "1B12.7", "icd10_code": "A183", "icd10_title": "Tuberculosis of intestines, peritoneum and mesenteric glands" }, { "from_icd11": "1B12.7", "icd10_code": "A188", "icd10_title": "Tuberculosis of other specified organs" }, { "from_icd11": "1B12.7", "icd10_code": "K230", "icd10_title": "" }, { "from_icd11": "1B12.7", "icd10_code": "K673", "icd10_title": "" }, { "from_icd11": "1B12.7", "icd10_code": "K93", "icd10_title": "" } ]
R180
Malignant ascites
The term CLOCC has previously been known by a variety of terms, including mild encephalitis/ encephalopathy with reversible splenial lesion , reversible splenial lesion syndrome or as transient splenial lesions . It has now been proposed as CLOCC to better reflect the underlying pathophysiology and the concept that these lesions are not always strictly splenial, not always reversible and not always associated with encephalopathy ; however, nomenclature in the literature is inconsistent. Whilst most cases present with signs and symptoms of encephalopathy or encephalitis, there are cases where only a headache or fever without neurological signs or symptoms are present . Our case did not have encephalopathy but did have a worsening headache with fever, had the classical pattern of a high T2 signal, a low T1 signal, restricted diffusion and a lack of contrast enhancement at the splenium of the corpus callosum which was notably reversible as evidenced by a normal subsequent MRI. Whilst these neuroimaging findings are not typical of TBM, the concomitant meningeal enhancement, multiple small tuberculomas and, importantly, the presence of M. Tuberculosis in the CSF, confirms the diagnosis. Given the absence of known household exposure to TB and the age of our case, we propose that he acquired TB in a community setting where young adolescents with infectious TB often socialise and gather, e.g., schools .
4.160156
0.708984
sec[2]/p[1]
en
0.999998
40278769
https://doi.org/10.3390/tropicalmed10040096
[ "encephalopathy", "reversible", "splenial", "always", "clocc", "known", "encephalitis", "lesion", "lesions", "that" ]
[ { "code": "8E47", "title": "Encephalopathy, not elsewhere classified" }, { "code": "8D43.0Y&XM0ZH6", "title": "Encephalopathy due to lead" }, { "code": "NA07.0Y", "title": "Other specified concussion" }, { "code": "8D43.0Z", "title": "Encephalopathy due to toxicity, unspecified" }, { "code": "NE80.3", "title": "Other serum reactions" }, { "code": "ME0A", "title": "Visible peristalsis" }, { "code": "9C85.Y", "title": "Other specified irregular eye movements" }, { "code": "GB01.0", "title": "Torsion of testis" }, { "code": "8B22.Y", "title": "Other specified cerebrovascular disease" }, { "code": "DA09.0", "title": "Pulpitis" } ]
=== ICD-11 CODES FOUND === [8E47] Encephalopathy, not elsewhere classified Definition: Global brain dysfunction Also known as: Encephalopathy, not elsewhere classified | encephalopathy NEC | encephalopathy NOS | encephalopathy disease | encephalopathy syndrome [NA07.0Y] Other specified concussion Also known as: Other specified concussion | Dupré syndrome | Irritation of meninges | Traumatic encephalopathy [8D43.0Z] Encephalopathy due to toxicity, unspecified Also known as: Encephalopathy due to toxicity, unspecified | Encephalopathy due to toxicity | toxic encephalopathy | toxic brain fever | toxic brain inflammation [NE80.3] Other serum reactions Also known as: Other serum reactions | Allergic reaction to serum | serum allergy | Complications of vaccination, protein sickness | Protein sickness Excludes: serum hepatitis [ME0A] Visible peristalsis Definition: The wavelike increased peristaltic motions of the intestines by which contents are forced onward toward the opening in such a way that they become visible through the abdominal walls by visual examination. Also known as: Visible peristalsis | Hyperperistalsis | Reverse peristalsis [9C85.Y] Other specified irregular eye movements Also known as: Other specified irregular eye movements | Oculomasticatory myorhythmia | Oculofacioskeletal myorhythmia | Spontaneous eye movement in unconscious patients | Ocular bobbing [GB01.0] Torsion of testis Definition: A condition of the testes, caused by determinants arising during the antenatal period, or exposure to cold temperatures. This condition is characterised by twisting of the spermatic cord, ischaemia of the testis, severe pain, tenderness, and decreased or absent cremasteric reflex. Confirmation is by imaging. Also known as: Torsion of testis | Torsion of spermatic cord | testicular torsion | torsion of spermatic cord NOS | Torsion of testis with reversible ischemia of the testis Includes: Torsion of spermatic cord [8B22.Y] Other specified cerebrovascular disease Also known as: Other specified cerebrovascular disease | Posterior reversible encephalopathy | Multiple or bilateral precerebral artery syndromes | multiple or bilateral precerebral artery syndromes, course of resolution unspecified | precerebral artery insufficiency NOS [DA09.0] Pulpitis Definition: Inflammation of pulpal tissue resulting from irritating factors of diverse nature such as bacterial, hyperaemic, chemical or thermal that act directly or indirectly on the dental pulp. Also known as: Pulpitis | Pulpitis NOS | Suppurative pulpitis | Acute pulpitis | Chronic pulpitis Includes: Suppurative pulpitis === GRAPH WALKS === --- Walk 1 --- [8E47] Encephalopathy, not elsewhere classified Def: Global brain dysfunction... --RELATED_TO--> [?] Hepatic encephalopathy Def: Hepatic encephalopathy is a complication of liver cirrhosis and a hallmark of acute liver failure, and is also observed in patients with portosystemic shunts without cirrhosis. Hepatic encephalopathy ... --CHILD--> [?] Hepatic encephalopathy, stage 2 --- Walk 2 --- [8E47] Encephalopathy, not elsewhere classified Def: Global brain dysfunction... --RELATED_TO--> [?] Hepatic encephalopathy Def: Hepatic encephalopathy is a complication of liver cirrhosis and a hallmark of acute liver failure, and is also observed in patients with portosystemic shunts without cirrhosis. Hepatic encephalopathy ... --PARENT--> [?] Certain specified diseases of liver Def: This is a group of conditions characterised as being in or associated with the liver that are not classified elsewhere.... --- Walk 3 --- [NA07.0Y] Other specified concussion --PARENT--> [NA07.0] Concussion Def: Loss or diminution of consciousness due to injury.... --CHILD--> [NA07.01] Concussion with incomplete loss of consciousness without amnesia --- Walk 4 --- [NA07.0Y] Other specified concussion --PARENT--> [NA07.0] Concussion Def: Loss or diminution of consciousness due to injury.... --CHILD--> [NA07.02] Concussion with loss of consciousness, short duration of less than 30 minutes --- Walk 5 --- [8D43.0Z] Encephalopathy due to toxicity, unspecified --PARENT--> [8D43.0] Encephalopathy due to toxicity --CHILD--> [8D43.0Y] Other specified encephalopathy due to toxicity --- Walk 6 --- [8D43.0Z] Encephalopathy due to toxicity, unspecified --PARENT--> [8D43.0] Encephalopathy due to toxicity --CHILD--> [8D43.0Y] Other specified encephalopathy due to toxicity
[ "[8E47] Encephalopathy, not elsewhere classified\n Def: Global brain dysfunction...\n --RELATED_TO--> [?] Hepatic encephalopathy\n Def: Hepatic encephalopathy is a complication of liver cirrhosis and a hallmark of acute liver failure, and is also observed in patients with portosystemic shunts without cirrhosis. Hepatic encephalopathy ...\n --CHILD--> [?] Hepatic encephalopathy, stage 2", "[8E47] Encephalopathy, not elsewhere classified\n Def: Global brain dysfunction...\n --RELATED_TO--> [?] Hepatic encephalopathy\n Def: Hepatic encephalopathy is a complication of liver cirrhosis and a hallmark of acute liver failure, and is also observed in patients with portosystemic shunts without cirrhosis. Hepatic encephalopathy ...\n --PARENT--> [?] Certain specified diseases of liver\n Def: This is a group of conditions characterised as being in or associated with the liver that are not classified elsewhere....", "[NA07.0Y] Other specified concussion\n --PARENT--> [NA07.0] Concussion\n Def: Loss or diminution of consciousness due to injury....\n --CHILD--> [NA07.01] Concussion with incomplete loss of consciousness without amnesia", "[NA07.0Y] Other specified concussion\n --PARENT--> [NA07.0] Concussion\n Def: Loss or diminution of consciousness due to injury....\n --CHILD--> [NA07.02] Concussion with loss of consciousness, short duration of less than 30 minutes", "[8D43.0Z] Encephalopathy due to toxicity, unspecified\n --PARENT--> [8D43.0] Encephalopathy due to toxicity\n --CHILD--> [8D43.0Y] Other specified encephalopathy due to toxicity", "[8D43.0Z] Encephalopathy due to toxicity, unspecified\n --PARENT--> [8D43.0] Encephalopathy due to toxicity\n --CHILD--> [8D43.0Y] Other specified encephalopathy due to toxicity" ]
8E47
Encephalopathy, not elsewhere classified
[ { "from_icd11": "8E47", "icd10_code": "G9349", "icd10_title": "Other encephalopathy" }, { "from_icd11": "8E47", "icd10_code": "G9340", "icd10_title": "Encephalopathy, unspecified" }, { "from_icd11": "8E47", "icd10_code": "G9341", "icd10_title": "Metabolic encephalopathy" }, { "from_icd11": "8E47", "icd10_code": "G934", "icd10_title": "Other and unspecified encephalopathy" }, { "from_icd11": "8E47", "icd10_code": "G943", "icd10_title": "" }, { "from_icd11": "NA07.0Y", "icd10_code": "S060X0A", "icd10_title": "Concussion without loss of consciousness, initial encounter" }, { "from_icd11": "8D43.0Z", "icd10_code": "G92", "icd10_title": "Toxic encephalopathy" }, { "from_icd11": "NE80.3", "icd10_code": "T880XXA", "icd10_title": "Infection following immunization, initial encounter" }, { "from_icd11": "NE80.3", "icd10_code": "T8061XA", "icd10_title": "Other serum reaction due to administration of blood and blood products, initial encounter" }, { "from_icd11": "NE80.3", "icd10_code": "T8069XA", "icd10_title": "Other serum reaction due to other serum, initial encounter" }, { "from_icd11": "NE80.3", "icd10_code": "T8062XA", "icd10_title": "Other serum reaction due to vaccination, initial encounter" }, { "from_icd11": "NE80.3", "icd10_code": "T806", "icd10_title": "Other serum reactions" }, { "from_icd11": "NE80.3", "icd10_code": "T880", "icd10_title": "Infection following immunization" }, { "from_icd11": "ME0A", "icd10_code": "R192", "icd10_title": "Visible peristalsis" }, { "from_icd11": "GB01.0", "icd10_code": "N4400", "icd10_title": "Torsion of testis, unspecified" } ]
G9349
Other encephalopathy
Another distinctive feature of this case is the presence of elevated anticardiolipin antibodies, which raised our suspicion of APS. At the three-month follow-up, despite the patient's compliance with NOAC anticoagulation following discharge, he presented with a new thrombotic event, specifically left femoral-popliteal venous axis thrombosis. The cardiolipin antibody titer was repeated and remained elevated, confirming the diagnosis of APS. Many clinical trials have shown an increased risk of recurrent thrombotic events associated with NOACs compared with VKA in patients with APS. In 2021, a review was conducted on a limited number of patients to evaluate the efficacy of NOACs in the prevention of thrombotic events in patients with APS. The findings indicate that patients with arterial APS or triple positivity (anti-cardiolipin (aCL), anti-β2 glycoprotein I (β2GPI), and lupus anticoagulant (LAC)) should be treated with VKA, whereas those with venous APS and single or double positivity may be candidates for NOACs. However, further high-quality studies are required to confirm this. In the case of our patient, despite the diagnosis of venous APS and single positivity, a new thrombotic event occurred following initial treatment with Apixaban. Consequently, a switch to a VKA was deemed appropriate. So we stopped the NOAC and started Acenocoumarol with doses adjusted to maintain an INR between 2 and 3.
4.242188
0.905273
sec[2]/p[6]
en
0.999997
39588428
https://doi.org/10.7759/cureus.72425
[ "thrombotic", "patients", "venous", "noacs", "positivity", "this", "despite", "noac", "event", "cardiolipin" ]
[ { "code": "DD30.Z", "title": "Acute vascular disorders of intestine, unspecified" }, { "code": "JA61.Y", "title": "Other specified venous complications in pregnancy" }, { "code": "JB41.Y", "title": "Other specified venous complications in the puerperium" }, { "code": "BA41.Z", "title": "Acute myocardial infarction, unspecified" }, { "code": "DB61", "title": "Perianal venous thrombosis" }, { "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 === [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 [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 [JB41.Y] Other specified venous complications in the puerperium Also known as: Other specified venous complications in the puerperium | Genital varices in the puerperium | varix of vulva in puerperium | Postpartum varicose veins of legs | varicose veins of legs in the puerperium [BA41.Z] Acute myocardial infarction, unspecified Also known as: Acute myocardial infarction, unspecified | Acute myocardial infarction | cardiac attack | heart attack | acute cardiac infarction [DB61] Perianal venous thrombosis Definition: Extremely painful cherry like lesions under the perianal skin containing clotted blood have been attributed to rupture of a blood vessel with haematoma. However, histology confirmed that these lesions are thrombi lying within the thin-walled vessels of the external anal plexus. Also known as: Perianal venous thrombosis | thrombosed external pile | anal thrombosis | Perianal haematoma (nontraumatic) | perianal thrombosis Includes: perianal thrombosis | Perianal haematoma (nontraumatic) [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 --- [DD30.Z] Acute vascular disorders of intestine, unspecified --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--> [DD30.1] Acute mesenteric arterial ischaemia Def: Acute mesenteric ischemia is low flow states of mesenteric circulation, in which inadequate blood flow through the mesenteric circulation causes ischemia and eventual gangrene of the bowel wall. It ca... --- Walk 2 --- [DD30.Z] Acute vascular disorders of intestine, unspecified --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.... --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... --- Walk 3 --- [JA61.Y] Other specified venous complications in pregnancy --PARENT--> [JA61] Venous complications in pregnancy --CHILD--> [JA61.2] Superficial thrombophlebitis in pregnancy --- Walk 4 --- [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 5 --- [JB41.Y] Other specified venous complications in the puerperium --PARENT--> [JB41] Venous complications in the puerperium --CHILD--> [JB41.0] Superficial thrombophlebitis in the puerperium --- Walk 6 --- [JB41.Y] Other specified venous complications in the puerperium --PARENT--> [JB41] Venous complications in the puerperium --EXCLUDES--> [?] Venous complications in pregnancy
[ "[DD30.Z] Acute vascular disorders of intestine, unspecified\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--> [DD30.1] Acute mesenteric arterial ischaemia\n Def: Acute mesenteric ischemia is low flow states of mesenteric circulation, in which inadequate blood flow through the mesenteric circulation causes ischemia and eventual gangrene of the bowel wall. It ca...", "[DD30.Z] Acute vascular disorders of intestine, unspecified\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 --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...", "[JA61.Y] Other specified venous complications in pregnancy\n --PARENT--> [JA61] Venous complications in pregnancy\n --CHILD--> [JA61.2] Superficial thrombophlebitis in 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...", "[JB41.Y] Other specified venous complications in the puerperium\n --PARENT--> [JB41] Venous complications in the puerperium\n --CHILD--> [JB41.0] Superficial thrombophlebitis in the puerperium", "[JB41.Y] Other specified venous complications in the puerperium\n --PARENT--> [JB41] Venous complications in the puerperium\n --EXCLUDES--> [?] Venous complications in pregnancy" ]
DD30.Z
Acute vascular disorders of intestine, unspecified
[ { "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" }, { "from_icd11": "DD30.Z", "icd10_code": "K55021", "icd10_title": "Focal (segmental) acute infarction of small intestine" }, { "from_icd11": "DD30.Z", "icd10_code": "K55039", "icd10_title": "Acute (reversible) ischemia of large intestine, extent unspecified" }, { "from_icd11": "DD30.Z", "icd10_code": "K55059", "icd10_title": "Acute (reversible) ischemia of intestine, part and extent unspecified" }, { "from_icd11": "DD30.Z", "icd10_code": "K55042", "icd10_title": "Diffuse acute infarction of large intestine" }, { "from_icd11": "DD30.Z", "icd10_code": "K55041", "icd10_title": "Focal (segmental) acute infarction of large intestine" }, { "from_icd11": "DD30.Z", "icd10_code": "K55011", "icd10_title": "Focal (segmental) acute (reversible) ischemia of small intestine" }, { "from_icd11": "DD30.Z", "icd10_code": "K55012", "icd10_title": "Diffuse acute (reversible) ischemia of small intestine" }, { "from_icd11": "DD30.Z", "icd10_code": "K55049", "icd10_title": "Acute infarction of large intestine, extent unspecified" }, { "from_icd11": "DD30.Z", "icd10_code": "K55061", "icd10_title": "Focal (segmental) acute infarction of intestine, part unspecified" }, { "from_icd11": "DD30.Z", "icd10_code": "K55022", "icd10_title": "Diffuse acute infarction of small intestine" }, { "from_icd11": "DD30.Z", "icd10_code": "K55031", "icd10_title": "Focal (segmental) acute (reversible) ischemia of large intestine" }, { "from_icd11": "DD30.Z", "icd10_code": "K55032", "icd10_title": "Diffuse acute (reversible) ischemia of large intestine" } ]
K55019
Acute (reversible) ischemia of small intestine, extent unspecified
Discoid lupus erythematosus (DLE) is the most common form of chronic cutaneous lupus erythematosus (CCLE), typically affecting women of childbearing age . Discoid lupus erythematosus usually presents in sun-exposed areas such as the face, ears, and scalp and poses a high risk of morbidity due to its potential for skin atrophy and scarring . The pathophysiology of drug-induced lupus erythematosus (DILE) is incompletely understood yet thought to involve a preexposing genetic or epigenetic susceptibility, instigated as a result of drug biotransformation . Discoid lupus erythematosus is often associated with systemic lupus erythematosus (SLE), as up to 20% of patients with DLE may develop systemic involvement over time. Certain medications, including proton pump inhibitors, hydralazine, and procainamide, have been reported to trigger cutaneous and systemic lupus erythematosus, although no reports of semaglutide-induced DLE have been reported to date . Glucagon-like peptide-1 receptor agonists (GLP-1 RAs), such as semaglutide, are increasingly used for the treatment of type 2 diabetes and obesity, providing metabolic and cardiovascular benefits . The immunomodulating properties of these compounds have also been investigated for their potential to treat or potentiate autoimmune disease . Here, we present a case of possible DLE following the initiation of semaglutide (Ozempic) in an adult male patient.
4.3125
0.824219
sec[0]/p[0]
en
0.999995
40330408
https://doi.org/10.7759/cureus.81663
[ "lupus", "erythematosus", "discoid", "systemic", "semaglutide", "cutaneous", "potential", "drug", "induced", "common" ]
[ { "code": "EB51.0", "title": "Discoid lupus erythematosus" }, { "code": "1B12.8", "title": "Cutaneous tuberculosis" }, { "code": "EB51.Y", "title": "Other specified chronic cutaneous lupus erythematosus" }, { "code": "4A40.0Y/BB20.Y", "title": "Pericarditis in systemic lupus erythematosus" }, { "code": "4A40.0Y", "title": "Other specified systemic lupus erythematosus" }, { "code": "ME64.0", "title": "Erythema" }, { "code": "EB10", "title": "Diffuse inflammatory erythemas" }, { "code": "4A40.Z", "title": "Lupus erythematosus, unspecified" }, { "code": "EB11", "title": "Annular erythema" }, { "code": "CA0Y", "title": "Other specified upper respiratory tract disorders" } ]
=== ICD-11 CODES FOUND === [EB51.0] Discoid lupus erythematosus Definition: Discoid lupus erythematosus is characterised by the presence of discoid plaques showing varying degrees of oedema, erythema, scaling, follicular plugging and atrophy. It typically involves the face, ears and scalp, but widespread dissemination may occur. It can cause marked disfigurement with prominent facial scarring and permanent hair loss. Also known as: Discoid lupus erythematosus | CDLE - [Chronic discoid lupus erythematosus] | DLE - [Discoid lupus erythematosus] | Chronic discoid lupus erythematosus | discoid lupus NOS [1B12.8] Cutaneous tuberculosis Definition: Tuberculosis involving the skin and mucous membranes including lupus vulgaris, scrofuloderma and periorificial tuberculosis. Also known as: Cutaneous tuberculosis | Tuberculosis of skin | Tuberculosis cutis | Tuberculous chancre | Primary inoculation tuberculosis Excludes: Tuberculids | Skin complications of BCG immunisation [EB51.Y] Other specified chronic cutaneous lupus erythematosus Also known as: Other specified chronic cutaneous lupus erythematosus | Verrucous lupus erythematosus | Warty lupus erythematosus | Lupus erythematosus tumidus | Tumid lupus erythematosus [4A40.0Y] Other specified systemic lupus erythematosus Also known as: Other specified systemic lupus erythematosus | Systemic lupus erythematosus with vasculitis | Systemic lupus erythematosus with neuropsychiatric involvement | lupus encephalopathy | Systemic lupus erythematosus with encephalitis Includes: Systemic lupus erythematosus with lung involvement | Systemic lupus erythematosus with kidney involvement [ME64.0] Erythema Definition: Redness of skin due to the presence of increased amounts of oxygenated haemoglobin within dilated skin capillaries. It may be due to localised or generalised inflammatory processes but may result from increased cutaneous blood flow following exertion or associated with pyrexia. Also known as: Erythema [EB10] Diffuse inflammatory erythemas Definition: A group of disorders characterised by diffuse redness of the skin. They may be due to drugs, viral infections or circulating toxins but frequently a precise aetiology cannot be determined. Also known as: Diffuse inflammatory erythemas | Erythroderma | Exfoliative dermatitis | Toxic erythema | Exanthematous rash [4A40.Z] Lupus erythematosus, unspecified Also known as: Lupus erythematosus, unspecified | Lupus erythematosus | LE - [lupus erythematosus] [EB11] Annular erythema Definition: Annular erythema is the term given to a group of chronic annular and gyrate eruptions in which irregular rings and arcs of elevated erythema form from initial inflammatory papules which slowly enlarge whilst clearing centrally. The lesions are usually located on the buttocks, thighs and upper arms, but any area may be involved. The condition may persist for months to years. In the majority of cases the aetiology remains obscure. Also known as: Annular erythema | Erythema annulare | Erythema annulare centrifugum [CA0Y] Other specified upper respiratory tract disorders Also known as: Other specified upper respiratory tract disorders | Acute adenoiditis | adenoid infection | Pharyngotonsillitis | tonsillopharyngitis === GRAPH WALKS === --- Walk 1 --- [EB51.0] Discoid lupus erythematosus Def: Discoid lupus erythematosus is characterised by the presence of discoid plaques showing varying degrees of oedema, erythema, scaling, follicular plugging and atrophy. It typically involves the face, e... --PARENT--> [EB51] Chronic cutaneous lupus erythematosus Def: Chronic cutaneous lupus erythematosus (LE) is characterised by the presence of circumscribed cutaneous plaques showing varying degrees of oedema, erythema, scaling, follicular plugging and atrophy. It... --EXCLUDES--> [?] Systemic lupus erythematosus Def: Systemic lupus erythematosus (SLE) is a clinically multisystem disease, which is autoimmune in origin and is characterised by the presence of autoantibodies directed against nuclear antigens. Manifest... --- Walk 2 --- [EB51.0] Discoid lupus erythematosus Def: Discoid lupus erythematosus is characterised by the presence of discoid plaques showing varying degrees of oedema, erythema, scaling, follicular plugging and atrophy. It typically involves the face, e... --PARENT--> [EB51] Chronic cutaneous lupus erythematosus Def: Chronic cutaneous lupus erythematosus (LE) is characterised by the presence of circumscribed cutaneous plaques showing varying degrees of oedema, erythema, scaling, follicular plugging and atrophy. It... --CHILD--> [EB51.Z] Chronic cutaneous lupus erythematosus, unspecified --- Walk 3 --- [1B12.8] Cutaneous tuberculosis Def: Tuberculosis involving the skin and mucous membranes including lupus vulgaris, scrofuloderma and periorificial tuberculosis.... --EXCLUDES--> [?] Skin complications of BCG immunisation Def: Complications secondary to immunization with attenuated Mycobacterium bovis (Bacillus Calmette-Guérin or BCG).... --CHILD--> [?] BCG-induced lupus vulgaris Def: Lupus vulgaris resulting from BCG immunization [Dermatology TAG]... --- Walk 4 --- [1B12.8] Cutaneous tuberculosis Def: Tuberculosis involving the skin and mucous membranes including lupus vulgaris, scrofuloderma and periorificial tuberculosis.... --RELATED_TO--> [?] Acute miliary cutaneous tuberculosis Def: Acute miliary cutaneous tuberculosis is a disseminated form of tuberculosis due to haematogenous spread. It may be a component of generalised miliary tuberculosis but the underlying disease may not be... --PARENT--> [?] Acute miliary tuberculosis of a single specified site Def: A disease caused by an infection with the bacteria Mycobacterium tuberculosis that is disseminated through the body, and affecting a specific body site. This disease is characterised by numerous small... --- Walk 5 --- [EB51.Y] Other specified chronic cutaneous lupus erythematosus --PARENT--> [EB51] Chronic cutaneous lupus erythematosus Def: Chronic cutaneous lupus erythematosus (LE) is characterised by the presence of circumscribed cutaneous plaques showing varying degrees of oedema, erythema, scaling, follicular plugging and atrophy. It... --EXCLUDES--> [?] Systemic lupus erythematosus Def: Systemic lupus erythematosus (SLE) is a clinically multisystem disease, which is autoimmune in origin and is characterised by the presence of autoantibodies directed against nuclear antigens. Manifest... --- Walk 6 --- [EB51.Y] Other specified chronic cutaneous lupus erythematosus --PARENT--> [EB51] Chronic cutaneous lupus erythematosus Def: Chronic cutaneous lupus erythematosus (LE) is characterised by the presence of circumscribed cutaneous plaques showing varying degrees of oedema, erythema, scaling, follicular plugging and atrophy. It... --EXCLUDES--> [?] Systemic lupus erythematosus Def: Systemic lupus erythematosus (SLE) is a clinically multisystem disease, which is autoimmune in origin and is characterised by the presence of autoantibodies directed against nuclear antigens. Manifest...
[ "[EB51.0] Discoid lupus erythematosus\n Def: Discoid lupus erythematosus is characterised by the presence of discoid plaques showing varying degrees of oedema, erythema, scaling, follicular plugging and atrophy. It typically involves the face, e...\n --PARENT--> [EB51] Chronic cutaneous lupus erythematosus\n Def: Chronic cutaneous lupus erythematosus (LE) is characterised by the presence of circumscribed cutaneous plaques showing varying degrees of oedema, erythema, scaling, follicular plugging and atrophy. It...\n --EXCLUDES--> [?] Systemic lupus erythematosus\n Def: Systemic lupus erythematosus (SLE) is a clinically multisystem disease, which is autoimmune in origin and is characterised by the presence of autoantibodies directed against nuclear antigens. Manifest...", "[EB51.0] Discoid lupus erythematosus\n Def: Discoid lupus erythematosus is characterised by the presence of discoid plaques showing varying degrees of oedema, erythema, scaling, follicular plugging and atrophy. It typically involves the face, e...\n --PARENT--> [EB51] Chronic cutaneous lupus erythematosus\n Def: Chronic cutaneous lupus erythematosus (LE) is characterised by the presence of circumscribed cutaneous plaques showing varying degrees of oedema, erythema, scaling, follicular plugging and atrophy. It...\n --CHILD--> [EB51.Z] Chronic cutaneous lupus erythematosus, unspecified", "[1B12.8] Cutaneous tuberculosis\n Def: Tuberculosis involving the skin and mucous membranes including lupus vulgaris, scrofuloderma and periorificial tuberculosis....\n --EXCLUDES--> [?] Skin complications of BCG immunisation\n Def: Complications secondary to immunization with attenuated Mycobacterium bovis (Bacillus Calmette-Guérin or BCG)....\n --CHILD--> [?] BCG-induced lupus vulgaris\n Def: Lupus vulgaris resulting from BCG immunization [Dermatology TAG]...", "[1B12.8] Cutaneous tuberculosis\n Def: Tuberculosis involving the skin and mucous membranes including lupus vulgaris, scrofuloderma and periorificial tuberculosis....\n --RELATED_TO--> [?] Acute miliary cutaneous tuberculosis\n Def: Acute miliary cutaneous tuberculosis is a disseminated form of tuberculosis due to haematogenous spread. It may be a component of generalised miliary tuberculosis but the underlying disease may not be...\n --PARENT--> [?] Acute miliary tuberculosis of a single specified site\n Def: A disease caused by an infection with the bacteria Mycobacterium tuberculosis that is disseminated through the body, and affecting a specific body site. This disease is characterised by numerous small...", "[EB51.Y] Other specified chronic cutaneous lupus erythematosus\n --PARENT--> [EB51] Chronic cutaneous lupus erythematosus\n Def: Chronic cutaneous lupus erythematosus (LE) is characterised by the presence of circumscribed cutaneous plaques showing varying degrees of oedema, erythema, scaling, follicular plugging and atrophy. It...\n --EXCLUDES--> [?] Systemic lupus erythematosus\n Def: Systemic lupus erythematosus (SLE) is a clinically multisystem disease, which is autoimmune in origin and is characterised by the presence of autoantibodies directed against nuclear antigens. Manifest...", "[EB51.Y] Other specified chronic cutaneous lupus erythematosus\n --PARENT--> [EB51] Chronic cutaneous lupus erythematosus\n Def: Chronic cutaneous lupus erythematosus (LE) is characterised by the presence of circumscribed cutaneous plaques showing varying degrees of oedema, erythema, scaling, follicular plugging and atrophy. It...\n --EXCLUDES--> [?] Systemic lupus erythematosus\n Def: Systemic lupus erythematosus (SLE) is a clinically multisystem disease, which is autoimmune in origin and is characterised by the presence of autoantibodies directed against nuclear antigens. Manifest..." ]
EB51.0
Discoid lupus erythematosus
[ { "from_icd11": "EB51.0", "icd10_code": "L932", "icd10_title": "Other local lupus erythematosus" }, { "from_icd11": "1B12.8", "icd10_code": "A184", "icd10_title": "Tuberculosis of skin and subcutaneous tissue" }, { "from_icd11": "ME64.0", "icd10_code": "L539", "icd10_title": "Erythematous condition, unspecified" }, { "from_icd11": "ME64.0", "icd10_code": "L54", "icd10_title": "Erythema in diseases classified elsewhere" }, { "from_icd11": "ME64.0", "icd10_code": "L548", "icd10_title": "" }, { "from_icd11": "EB10", "icd10_code": "L538", "icd10_title": "Other specified erythematous conditions" }, { "from_icd11": "EB10", "icd10_code": "L530", "icd10_title": "Toxic erythema" }, { "from_icd11": "EB10", "icd10_code": "L26", "icd10_title": "Exfoliative dermatitis" }, { "from_icd11": "4A40.Z", "icd10_code": "L80-L99", "icd10_title": "" }, { "from_icd11": "4A40.Z", "icd10_code": "L93", "icd10_title": "Lupus erythematosus" }, { "from_icd11": "EB11", "icd10_code": "L531", "icd10_title": "Erythema annulare centrifugum" }, { "from_icd11": "EB11", "icd10_code": "L532", "icd10_title": "Erythema marginatum" }, { "from_icd11": "EB11", "icd10_code": "L533", "icd10_title": "Other chronic figurate erythema" } ]
L932
Other local lupus erythematosus
A 46-year-old left-handed male presented with a chief complaint of left vertex headache, 8/10 pain, after a motor vehicle collision, with head strike and loss of consciousness. The patient was GCS15 and had left eye ecchymosis and facial swelling. The patient’s pre-stimulation EMF data showed localization of the site of brain injury to SOI6 (left motor cortex and deeper structures) and OS3 (right sensory cortex and deeper structures) and revealed a pair of peak and valley at 7.9 Hz (red arrow) which was selected as the FOI . Continuous EMF stimulation at 7.9 Hz, 10.0 V over 3 minutes was applied . Post-stimulation, the patient reported a headache improved to 2/10 pain, and the post-stimulation EMF showed similar amplitude (red arrow) between SOI and OS . Given that the patient still endorsed a headache, and post-stimulation EMF recording and assessment did not demonstrate a sustained change, a longer duration of continuous EMF stimulation was delivered, aiming to achieve resolution of his headache. Therefore, continuous EMF stimulation at 7.9 Hz, 10.0 V over 5 minutes was delivered . Post-stimulation, the patient reported resolution of his headache from an initial headache of 8/10. Post-stimulation EMF showed the SOI was at a peak and higher amplitude than that of the OS . Given the complete resolution of his headache, there was no indication to increase the duration of stimulation to 8 minutes.
3.945313
0.979004
sec[2]/p[2]
en
0.999997
PMC12101138
https://doi.org/10.7759/cureus.84653
[ "stimulation", "headache", "continuous", "minutes", "resolution", "pain", "motor", "cortex", "deeper", "structures" ]
[ { "code": "MB72", "title": "Results of function studies of the nervous system" }, { "code": "4A01.0Y", "title": "Other specified immunodeficiencies with predominantly antibody defects" }, { "code": "NE60", "title": "Harmful effects of drugs, medicaments or biological substances, not elsewhere classified" }, { "code": "8D85", "title": "Autonomic nervous system disorder due to substances" }, { "code": "6C46.3", "title": "Stimulant intoxication including amphetamines, methamphetamine or methcathinone" }, { "code": "MB4D", "title": "Headache, not elsewhere classified" }, { "code": "8A8Z", "title": "Headache disorders, unspecified" }, { "code": "8A8Y", "title": "Other specified headache disorders" }, { "code": "8A82", "title": "Trigeminal autonomic cephalalgias" }, { "code": "8A83", "title": "Other primary headache disorder" } ]
=== ICD-11 CODES FOUND === [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] [4A01.0Y] Other specified immunodeficiencies with predominantly antibody defects Also known as: Other specified immunodeficiencies with predominantly antibody defects | Common variable immunodeficiency | B-cell activating factor receptor deficiency | BAFF - [ B-cell activating factor] receptor deficiency | Cluster of differentiation 19 deficiency [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 [8D85] Autonomic nervous system disorder due to substances Also known as: Autonomic nervous system disorder due to substances | Serotonin syndrome | Seritonergic syndrome | Autonomic disorder due to stimulant intoxication | Autonomic disorder due to Wernicke-Korsakoff syndrome [6C46.3] Stimulant intoxication including amphetamines, methamphetamine or methcathinone Definition: Stimulant intoxication including amphetamines, methamphetamine and methcathinone but excluding caffeine, cocaine and synthetic cathinones is a clinically significant transient condition that develops during or shortly after the consumption of amphetamine or other stimulants that is characterised by disturbances in consciousness, cognition, perception, affect, behaviour, or coordination. These disturbances are caused by the known pharmacological effects of amphetamine or other stimulants and thei Also known as: Stimulant intoxication including amphetamines, methamphetamine or methcathinone | Amphetamine or certain specified stimulant intoxication | Amphetamine intoxication | Methamphetamine intoxication | Acute methamphetamine intoxication Excludes: amphetamine poisoning | Caffeine intoxication | Cocaine intoxication [MB4D] Headache, not elsewhere classified Definition: 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. Also known as: Headache, not elsewhere classified | cephalalgia | cephalgia | cephalodynia | pain in head NOS Excludes: Trigeminal neuralgia | Atypical facial pain | Acute headache, not elsewhere classified [8A8Z] Headache disorders, unspecified Also known as: Headache disorders, unspecified [8A8Y] Other specified headache disorders Also known as: Other specified headache disorders [8A82] Trigeminal autonomic cephalalgias Definition: A group of related primary headache disorders essentially characterised by unilateral headache and trigeminal autonomic activation. In most but not all of these disorders, the headache is short-lasting and very frequently recurring, but sometimes remitting for long periods. Also known as: Trigeminal autonomic cephalalgias | Cluster headache | Horton headache | Episodic cluster headache | Chronic cluster headache [8A83] Other primary headache disorder Definition: A group of clinically heterogeneous headache disorders, believed to be primary. Although largely unrelated, they fall into four categories: headaches associated with physical exertion; headaches attributed to direct physical but innocuous stimuli; epicranial headaches; and other miscellaneous primary headache disorders. Also known as: Other primary headache disorder | Primary cough headache | Primary exercise headache | Primary headache associated with sexual activity | Preorgasmic headache === GRAPH WALKS === --- Walk 1 --- [MB72] Results of function studies of the nervous system --PARENT--> [?] Clinical findings in the nervous system --CHILD--> [MB71] Clinical findings on diagnostic imaging of central nervous system Def: Clinical findings on diagnostic imaging of central nervous system is findings on diagnostic imaging of the brain or the spinal cord which don't appear in normal status of the body. Diagnostic imaging ... --- Walk 2 --- [MB72] Results of function studies of the nervous system --PARENT--> [?] Clinical findings in the nervous system --CHILD--> [MB70] Clinical findings in cerebrospinal fluid --- Walk 3 --- [4A01.0Y] Other specified immunodeficiencies with predominantly antibody defects --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 4 --- [4A01.0Y] Other specified immunodeficiencies with predominantly antibody defects --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 5 --- [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 6 --- [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,... --CHILD--> [?] Severe alcohol intoxication Def: Severe alcohol intoxication is a clinically significant transient condition that develops during or shortly after the administration of alcohol that is characterised by obvious disturbance in consciou...
[ "[MB72] Results of function studies of the nervous system\n --PARENT--> [?] Clinical findings in the nervous system\n --CHILD--> [MB71] Clinical findings on diagnostic imaging of central nervous system\n Def: Clinical findings on diagnostic imaging of central nervous system is findings on diagnostic imaging of the brain or the spinal cord which don't appear in normal status of the body. Diagnostic imaging ...", "[MB72] Results of function studies of the nervous system\n --PARENT--> [?] Clinical findings in the nervous system\n --CHILD--> [MB70] Clinical findings in cerebrospinal fluid", "[4A01.0Y] Other specified immunodeficiencies with predominantly antibody defects\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", "[4A01.0Y] Other specified immunodeficiencies with predominantly antibody defects\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", "[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 ...", "[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 --CHILD--> [?] Severe alcohol intoxication\n Def: Severe alcohol intoxication is a clinically significant transient condition that develops during or shortly after the administration of alcohol that is characterised by obvious disturbance in consciou..." ]
MB72
Results of function studies of the nervous system
[ { "from_icd11": "MB72", "icd10_code": "R29818", "icd10_title": "Other symptoms and signs involving the nervous system" }, { "from_icd11": "MB72", "icd10_code": "R29810", "icd10_title": "Facial weakness" }, { "from_icd11": "MB72", "icd10_code": "R29898", "icd10_title": "Other symptoms and signs involving the musculoskeletal system" }, { "from_icd11": "MB72", "icd10_code": "R9402", "icd10_title": "Abnormal brain scan" }, { "from_icd11": "MB72", "icd10_code": "R9401", "icd10_title": "Abnormal electroencephalogram [EEG]" }, { "from_icd11": "MB72", "icd10_code": "R29890", "icd10_title": "Loss of height" }, { "from_icd11": "MB72", "icd10_code": "R9409", "icd10_title": "Abnormal results of other function studies of central nervous system" }, { "from_icd11": "MB72", "icd10_code": "R298", "icd10_title": "Other symptoms and signs involving the nervous and musculoskeletal systems" }, { "from_icd11": "MB72", "icd10_code": "R940", "icd10_title": "Abnormal results of function studies of central nervous system" }, { "from_icd11": "MB72", "icd10_code": "R941", "icd10_title": "Abnormal results of function studies of peripheral nervous system and special senses" }, { "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" } ]
R29818
Other symptoms and signs involving the nervous system
In October 2002, an immature male New Zealand fur seal was taken into rehabilitation care after being found hauled out on a beach near Narooma, New South Wales (NSW), Australia, in an emaciated body condition and exhibiting dehydration, severe anemia, and several deep skin wounds over the right hip and right hind flipper, presumably associated with a failed predation attempt by a shark. Upon examination, the seal was noted to have several small raised, sometimes pedunculated and coalescing papillary masses on the roof of the mouth with similar but smaller lesions, evident on the caudoventral right and ventral left aspects of the tongue . There was also a circumferential zone of mucosal pallor around the right mandibular canine tooth . Biopsies of the papillary masses were taken from the roof of the mouth and tongue region in February 2003. Fig. 1 Papillary proliferations, cellular atypia, and the presence of koilocytes in oral lesions. Multifocally coalescing sessile to papillary proliferations of the palatine and lingual epithelium of a New Zealand fur seal Registry #3254 ( a , b ). A zone of mucosal pallor surrounding the mandibular canine tooth ( c ). Demarcated lingual epithelial proliferation, with basophilia, and expansion of the stratum spinosum and stratum corneum ( d —inset higher magnification of the lesion demonstrating cellular atypia and the presence of koilocytes—black arrowheads).
3.982422
0.489746
sec[1]/sec[1]/p[0]
en
0.999997
PMC11721157
https://doi.org/10.1038/s44298-024-00020-w
[ "papillary", "seal", "zealand", "several", "coalescing", "masses", "roof", "mouth", "lesions", "tongue" ]
[ { "code": "BE2Y", "title": "Other specified diseases of the circulatory system" }, { "code": "DA01.40&XA00H5", "title": "Papillary hyperplasia of palate" }, { "code": "BC0Z", "title": "Heart valve diseases, unspecified" }, { "code": "9A60.0Z", "title": "Papillary conjunctivitis, unspecified" }, { "code": "DA03.2", "title": "Atrophy of tongue papillae" }, { "code": "3A50.01", "title": "Thalassaemic alpha-chain variants" }, { "code": "ND51.Y", "title": "Other specified injuries of spine or trunk, level unspecified" }, { "code": "ND53.Y", "title": "Other specified injuries of arm, level unspecified" }, { "code": "6D10.2", "title": "Severe personality disorder" }, { "code": "6D10.Z", "title": "Personality disorder, severity unspecified" } ]
=== ICD-11 CODES FOUND === [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 [BC0Z] Heart valve diseases, unspecified Also known as: Heart valve diseases, unspecified | chronic rheumatic heart disease with valvulitis | heart valve lesion NOS | valvulopathy NOS | valvular heart disease NOS [9A60.0Z] Papillary conjunctivitis, unspecified Also known as: Papillary conjunctivitis, unspecified | Papillary conjunctivitis [DA03.2] Atrophy of tongue papillae Also known as: Atrophy of tongue papillae | Atrophic glossitis | Hunter glossitis | Central papillary atrophy of the tongue Includes: Atrophic glossitis | Central papillary atrophy of the tongue [3A50.01] Thalassaemic alpha-chain variants Also known as: Thalassaemic alpha-chain variants | Haemoglobin Koya Dora | Haemoglobin Pakse | Haemoglobin Seal Rock | Haemoglobin Constant Spring [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 [ND53.Y] Other specified injuries of arm, level unspecified Also known as: Other specified injuries of arm, level unspecified | Superficial injury of arm, level unspecified | superficial injury of upper limb, level unspecified | Abrasion of arm, level unspecified | Contusion of arm, level unspecified [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 [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 === GRAPH WALKS === --- Walk 1 --- [BE2Y] Other specified diseases of the circulatory system --PARENT--> [11] Diseases of the circulatory system Def: This refers to diseases of the organ system that passes nutrients (such as amino acids, electrolytes and lymph), gases, hormones, blood cells, etc. to and from cells in the body to help fight diseases... --CHILD--> [?] Hypotension --- Walk 2 --- [BE2Y] Other specified diseases of the circulatory system --PARENT--> [11] Diseases of the circulatory system Def: This refers to diseases of the organ system that passes nutrients (such as amino acids, electrolytes and lymph), gases, hormones, blood cells, etc. to and from cells in the body to help fight diseases... --CHILD--> [?] Hypertensive diseases Def: Although a continuous association exists between higher blood pressure (BP) and increased cardiovascular disease risk, it is useful to categorize BP levels for clinical and public health decision maki... --- Walk 3 --- [BC0Z] Heart valve diseases, unspecified --PARENT--> [?] Heart valve diseases --CHILD--> [?] Mitral valve disease Def: This is a disorder of the heart in which the mitral valve does not close properly when the heart pumps out blood. It is the abnormal leaking of blood from the left ventricle through the mitral valve i... --- Walk 4 --- [BC0Z] Heart valve diseases, unspecified --PARENT--> [?] Heart valve diseases --EXCLUDES--> [?] Congenital anomaly of a ventriculo-arterial valve or adjacent regions Def: A congenital cardiovascular malformation of a ventriculo-arterial valve or its immediate subvalvar and supravalvar regions.... --- Walk 5 --- [9A60.0Z] Papillary conjunctivitis, unspecified --PARENT--> [9A60.0] Papillary conjunctivitis --PARENT--> [9A60] Conjunctivitis --- Walk 6 --- [9A60.0Z] Papillary conjunctivitis, unspecified --PARENT--> [9A60.0] Papillary conjunctivitis --CHILD--> [9A60.00] Giant papillary conjunctivitis Def: Giant papillary conjunctivitis is a nonallergic hypersensitivity inflammation of the ocular surface, most frequently to contact lenses, ocular prostheses, postoperative sutures, and scleral buckles....
[ "[BE2Y] Other specified diseases of the circulatory system\n --PARENT--> [11] Diseases of the circulatory system\n Def: This refers to diseases of the organ system that passes nutrients (such as amino acids, electrolytes and lymph), gases, hormones, blood cells, etc. to and from cells in the body to help fight diseases...\n --CHILD--> [?] Hypotension", "[BE2Y] Other specified diseases of the circulatory system\n --PARENT--> [11] Diseases of the circulatory system\n Def: This refers to diseases of the organ system that passes nutrients (such as amino acids, electrolytes and lymph), gases, hormones, blood cells, etc. to and from cells in the body to help fight diseases...\n --CHILD--> [?] Hypertensive diseases\n Def: Although a continuous association exists between higher blood pressure (BP) and increased cardiovascular disease risk, it is useful to categorize BP levels for clinical and public health decision maki...", "[BC0Z] Heart valve diseases, unspecified\n --PARENT--> [?] Heart valve diseases\n --CHILD--> [?] Mitral valve disease\n Def: This is a disorder of the heart in which the mitral valve does not close properly when the heart pumps out blood. It is the abnormal leaking of blood from the left ventricle through the mitral valve i...", "[BC0Z] Heart valve diseases, unspecified\n --PARENT--> [?] Heart valve diseases\n --EXCLUDES--> [?] Congenital anomaly of a ventriculo-arterial valve or adjacent regions\n Def: A congenital cardiovascular malformation of a ventriculo-arterial valve or its immediate subvalvar and supravalvar regions....", "[9A60.0Z] Papillary conjunctivitis, unspecified\n --PARENT--> [9A60.0] Papillary conjunctivitis\n --PARENT--> [9A60] Conjunctivitis", "[9A60.0Z] Papillary conjunctivitis, unspecified\n --PARENT--> [9A60.0] Papillary conjunctivitis\n --CHILD--> [9A60.00] Giant papillary conjunctivitis\n Def: Giant papillary conjunctivitis is a nonallergic hypersensitivity inflammation of the ocular surface, most frequently to contact lenses, ocular prostheses, postoperative sutures, and scleral buckles...." ]
BE2Y
Other specified diseases of the circulatory system
[ { "from_icd11": "BC0Z", "icd10_code": "I511", "icd10_title": "Rupture of chordae tendineae, not elsewhere classified" }, { "from_icd11": "BC0Z", "icd10_code": "I38", "icd10_title": "Endocarditis, valve unspecified" }, { "from_icd11": "BC0Z", "icd10_code": "I39", "icd10_title": "Endocarditis and heart valve disorders in diseases classified elsewhere" }, { "from_icd11": "BC0Z", "icd10_code": "I512", "icd10_title": "Rupture of papillary muscle, not elsewhere classified" }, { "from_icd11": "BC0Z", "icd10_code": "I05-I09", "icd10_title": "" }, { "from_icd11": "BC0Z", "icd10_code": "I05", "icd10_title": "Rheumatic mitral valve diseases" }, { "from_icd11": "BC0Z", "icd10_code": "I06", "icd10_title": "Rheumatic aortic valve diseases" }, { "from_icd11": "BC0Z", "icd10_code": "I08", "icd10_title": "Multiple valve diseases" }, { "from_icd11": "BC0Z", "icd10_code": "I34", "icd10_title": "Nonrheumatic mitral valve disorders" }, { "from_icd11": "BC0Z", "icd10_code": "I35", "icd10_title": "Nonrheumatic aortic valve disorders" }, { "from_icd11": "BC0Z", "icd10_code": "I36", "icd10_title": "Nonrheumatic tricuspid valve disorders" }, { "from_icd11": "BC0Z", "icd10_code": "I37", "icd10_title": "Nonrheumatic pulmonary valve disorders" }, { "from_icd11": "BC0Z", "icd10_code": "I398", "icd10_title": "" }, { "from_icd11": "9A60.0Z", "icd10_code": "H1010", "icd10_title": "Acute atopic conjunctivitis, unspecified eye" }, { "from_icd11": "9A60.0Z", "icd10_code": "H101", "icd10_title": "Acute atopic conjunctivitis" } ]
I511
Rupture of chordae tendineae, not elsewhere classified
A 61-year-old male with no past medical history presented to the emergency department with complaints of skin rash, fever, shortness of breath, and cough for about a week. On admission, he was found to be febrile (38.8°C or 101.8°F) and tachycardic (115 bpm). Physical exam showed mild pharyngeal erythema and a few coarse crackles at the lung bases and a maculopapular rash on the trunk, shoulders, and upper thighs. Laboratory findings showed leukocytosis of 15.0 K/mcl (normal: 4.5-11.0 K/mcl) with neutrophilia at 12.22 K/mcl (normal: 2.6-8.2 K/mcl), and mild eosinophilia of 0.36 K/mcl (normal: 00.0-0.35 K/mcl). Chest X-ray showed a right lower lung infiltrate, confirmed with computed tomography (CT) of the chest as well, which did not show pleural effusion or lymphadenopathy . A multiplex polymerase chain reaction (PCR) respiratory panel called BioFire (originally from France but with headquarters in Salt Lake City, Utah) that screens for both common viral and bacterial pathogens was performed on a nasopharyngeal swab sample, and it was positive for Mycoplasma pneumoniae and coronavirus NL63. Because the patient lives in an area endemic of coccidioidomycosis, Coccidioides spp. immunoglobulin M (IgM) and immunoglobulin G (IgG) detected using enzyme-immunoassay (EIA) (manufactured by Premier, Inc., Charlotte, North Carolina) on the patient’s serum were requested on admission and came back negative.
3.974609
0.974121
sec[1]/p[0]
en
0.999996
PMC12065599
https://doi.org/10.7759/cureus.82025
[ "rash", "lung", "chest", "immunoglobulin", "past", "emergency", "department", "complaints", "skin", "fever" ]
[ { "code": "ME66.6Z", "title": "Rash, unspecified" }, { "code": "ME66.6Y", "title": "Other specified rash" }, { "code": "ME62", "title": "Acute skin eruption of uncertain or unspecified nature" }, { "code": "ME63", "title": "Chronic skin disorder of uncertain or unspecified nature" }, { "code": "EA00", "title": "Viral exanthem due to unknown or unspecified agent" }, { "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" } ]
=== ICD-11 CODES FOUND === [ME66.6Z] Rash, unspecified Also known as: Rash, unspecified | Rash | skin rash NOS [ME66.6Y] Other specified rash Also known as: Other specified rash [ME62] Acute skin eruption of uncertain or unspecified nature Definition: A provisional diagnosis for an acute skin eruption of less than six weeks' duration of unknown, uncertain or unspecified nature. Also known as: Acute skin eruption of uncertain or unspecified nature | Acute skin eruption without established diagnosis | Acute rash | Acute pustular skin eruption Excludes: Drug eruptions [ME63] Chronic skin disorder of uncertain or unspecified nature Definition: A provisional diagnosis for a chronic skin disorder (of at least six weeks' duration) of unknown, uncertain or unspecified nature. Also known as: Chronic skin disorder of uncertain or unspecified nature | Chronic skin disorder without established diagnosis | Chronic rash [EA00] Viral exanthem due to unknown or unspecified agent Definition: An exanthematic rash with symptoms suggestive of a viral aetiology where the agent is either unknown or unspecified. Also known as: Viral exanthem due to unknown or unspecified agent | Viral exanthem | viral rash NOS | virus exanthema | nonspecific exanthematous viral infection [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 === GRAPH WALKS === --- Walk 1 --- [ME66.6Z] Rash, unspecified --PARENT--> [ME66.6] Rash Def: A non-specific term indicating the presence of an acquired skin disturbance to be used only when no more precise information is available.... --CHILD--> [ME66.60] Rash localised Def: A very non-specific term to denote a localised acquired visible alteration of the skin from normal in situations where a more precise description or diagnosis cannot be made. If a diagnosis cannot be ... --- Walk 2 --- [ME66.6Z] Rash, unspecified --PARENT--> [ME66.6] Rash Def: A non-specific term indicating the presence of an acquired skin disturbance to be used only when no more precise information is available.... --EXCLUDES--> [?] Chronic skin disorder of uncertain or unspecified nature Def: A provisional diagnosis for a chronic skin disorder (of at least six weeks' duration) of unknown, uncertain or unspecified nature.... --- Walk 3 --- [ME66.6Y] Other specified rash --PARENT--> [ME66.6] Rash Def: A non-specific term indicating the presence of an acquired skin disturbance to be used only when no more precise information is available.... --EXCLUDES--> [?] Chronic skin disorder of uncertain or unspecified nature Def: A provisional diagnosis for a chronic skin disorder (of at least six weeks' duration) of unknown, uncertain or unspecified nature.... --- Walk 4 --- [ME66.6Y] Other specified rash --PARENT--> [ME66.6] Rash Def: A non-specific term indicating the presence of an acquired skin disturbance to be used only when no more precise information is available.... --CHILD--> [ME66.61] Rash generalised Def: A very non-specific term to denote a widespread acquired visible alteration of the skin from normal in situations where a more precise description or diagnosis cannot be made. If a diagnosis cannot be... --- Walk 5 --- [ME62] Acute skin eruption of uncertain or unspecified nature Def: A provisional diagnosis for an acute skin eruption of less than six weeks' duration of unknown, uncertain 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--> [ME62] Acute skin eruption of uncertain or unspecified nature Def: A provisional diagnosis for an acute skin eruption of less than six weeks' duration of unknown, uncertain or unspecified nature.... --- Walk 6 --- [ME62] Acute skin eruption of uncertain or unspecified nature Def: A provisional diagnosis for an acute skin eruption of less than six weeks' duration of unknown, uncertain or unspecified nature.... --CHILD--> [ME62.2] Acute urticarial skin eruption Def: A provisional diagnosis for a skin eruption of unknown or uncertain nature which arises abruptly and consists of urticaria-like papules and plaques. Drugs are a common precipitant.... --PARENT--> [ME62] Acute skin eruption of uncertain or unspecified nature Def: A provisional diagnosis for an acute skin eruption of less than six weeks' duration of unknown, uncertain or unspecified nature....
[ "[ME66.6Z] Rash, unspecified\n --PARENT--> [ME66.6] Rash\n Def: A non-specific term indicating the presence of an acquired skin disturbance to be used only when no more precise information is available....\n --CHILD--> [ME66.60] Rash localised\n Def: A very non-specific term to denote a localised acquired visible alteration of the skin from normal in situations where a more precise description or diagnosis cannot be made. If a diagnosis cannot be ...", "[ME66.6Z] Rash, unspecified\n --PARENT--> [ME66.6] Rash\n Def: A non-specific term indicating the presence of an acquired skin disturbance to be used only when no more precise information is available....\n --EXCLUDES--> [?] Chronic skin disorder of uncertain or unspecified nature\n Def: A provisional diagnosis for a chronic skin disorder (of at least six weeks' duration) of unknown, uncertain or unspecified nature....", "[ME66.6Y] Other specified rash\n --PARENT--> [ME66.6] Rash\n Def: A non-specific term indicating the presence of an acquired skin disturbance to be used only when no more precise information is available....\n --EXCLUDES--> [?] Chronic skin disorder of uncertain or unspecified nature\n Def: A provisional diagnosis for a chronic skin disorder (of at least six weeks' duration) of unknown, uncertain or unspecified nature....", "[ME66.6Y] Other specified rash\n --PARENT--> [ME66.6] Rash\n Def: A non-specific term indicating the presence of an acquired skin disturbance to be used only when no more precise information is available....\n --CHILD--> [ME66.61] Rash generalised\n Def: A very non-specific term to denote a widespread acquired visible alteration of the skin from normal in situations where a more precise description or diagnosis cannot be made. If a diagnosis cannot be...", "[ME62] Acute skin eruption of uncertain or unspecified nature\n Def: A provisional diagnosis for an acute skin eruption of less than six weeks' duration of unknown, uncertain 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--> [ME62] Acute skin eruption of uncertain or unspecified nature\n Def: A provisional diagnosis for an acute skin eruption of less than six weeks' duration of unknown, uncertain or unspecified nature....", "[ME62] Acute skin eruption of uncertain or unspecified nature\n Def: A provisional diagnosis for an acute skin eruption of less than six weeks' duration of unknown, uncertain or unspecified nature....\n --CHILD--> [ME62.2] Acute urticarial skin eruption\n Def: A provisional diagnosis for a skin eruption of unknown or uncertain nature which arises abruptly and consists of urticaria-like papules and plaques. Drugs are a common precipitant....\n --PARENT--> [ME62] Acute skin eruption of uncertain or unspecified nature\n Def: A provisional diagnosis for an acute skin eruption of less than six weeks' duration of unknown, uncertain or unspecified nature...." ]
ME66.6Z
Rash, unspecified
[ { "from_icd11": "ME62", "icd10_code": "R21", "icd10_title": "Rash and other nonspecific skin eruption" }, { "from_icd11": "ME62", "icd10_code": "R20-R23", "icd10_title": "" }, { "from_icd11": "ME63", "icd10_code": "L989", "icd10_title": "Disorder of the skin and subcutaneous tissue, unspecified" }, { "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": "" } ]
R21
Rash and other nonspecific skin eruption
The second patient is a full-term girl, born with 2450 g after an intrauterine growth restriction and delivered via cesarean due to a bicornuate uterus. She is the second child of a non-consanguineous Caucasian couple, without any relevant medical history. On the 10th day of life, a blood count revealed severe hyporegenerative anemia and severe neutropenia ( Table 1 ). At 2 months old, hematologic and metabolic workup revealed persistent thrombocytopenia, significant fumaric aciduria, and slightly increased plasma amino acids alanine and glutamine. BM aspiration revealed a normal maturation of the three cell lines but with vacuolization of myeloid and erythroid precursors and ring sideroblasts (15%) . Due to the child's young age and low diagnostic added value, trephine biopsy was not performed. Acquired causes of sideroblastic anemia were ruled out based on normal copper levels, the absence of myelodysplastic syndrome on BMA, and the absence of toxic or drug intake. A genetic panel was also carried out and came back negative (no mutations in the SCL19A2, SLC25A19 genes TRK1). In addition to monthly RBC transfusions and occasional platelet transfusions, the patient received thiamine and riboflavin supplements until mtDNA results were available. However, these supplements did not improve her condition. mtDNA sequencing shows the presence of a heteroplasmic : m8483-13459 SLSMD, consistent with PS.
4.121094
0.97168
sec[0]/sec[1]/p[0]
en
0.999996
40420845
https://doi.org/10.1155/crpe/3076141
[ "anemia", "absence", "transfusions", "supplements", "mtdna", "full", "term", "girl", "born", "intrauterine" ]
[ { "code": "3A9Z", "title": "Anaemias or other erythrocyte disorders, unspecified" }, { "code": "KA8Y", "title": "Other specified haemorrhagic or haematological disorders of fetus or newborn" }, { "code": "3A70.11", "title": "Aplastic anaemia due to other external agents" }, { "code": "JB64.0", "title": "Anaemia complicating pregnancy, childbirth or the puerperium" }, { "code": "3A70.Z", "title": "Aplastic anaemia, unspecified" }, { "code": "8A68.Y", "title": "Other specified type of seizure" }, { "code": "LA75.1", "title": "Agenesis of lung" }, { "code": "8A66.1Z", "title": "Non-convulsive status epilepticus, unspecified" }, { "code": "LB20.0Y", "title": "Other specified structural developmental anomalies of liver" }, { "code": "QF01.Y", "title": "Other specified acquired absence of organs" } ]
=== ICD-11 CODES FOUND === [3A9Z] Anaemias or other erythrocyte disorders, unspecified Also known as: Anaemias or other erythrocyte disorders, unspecified | anaemia NOS | anaemic condition NOS | primary anaemia NOS | multifactorial anaemia NOS [KA8Y] Other specified haemorrhagic or haematological disorders of fetus or newborn Also known as: Other specified haemorrhagic or haematological disorders of fetus or newborn | Kasabach-Merritt syndrome | Blood dyscrasia of fetus or newborn | Other congenital anaemias, not elsewhere classified | newborn anaemia NOS [3A70.11] Aplastic anaemia due to other external agents Also known as: Aplastic anaemia due to other external agents | toxic anaemia | toxic aplastic anaemia | aplastic anaemia due to toxic cause [JB64.0] Anaemia complicating pregnancy, childbirth or the puerperium Definition: A condition of the circulatory system affecting pregnant females, characterised by a haemoglobin level below 11 grams per decilitre that complicates pregnancy, childbirth, or the puerperium. Also known as: Anaemia complicating pregnancy, childbirth or the puerperium | anaemia in mother complicating pregnancy, childbirth or puerperium | Anaemia of or complicating pregnancy | Anaemia of the puerperium | puerperal anaemia [3A70.Z] Aplastic anaemia, unspecified Also known as: Aplastic anaemia, unspecified | Aplastic anaemia | erythroid aplasia | AA - [aplastic anaemia] | haematopoietic aplasia [8A68.Y] Other specified type of seizure Also known as: Other specified type of seizure | Absence episode | Absence seizure episode | Pseudotetanus | Clonic seizure disorder [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 [8A66.1Z] Non-convulsive status epilepticus, unspecified Also known as: Non-convulsive status epilepticus, unspecified | Non-convulsive status epilepticus | Epileptic absence status | Petit mal status epilepticus | Petit-mal status [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 [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 === GRAPH WALKS === --- Walk 1 --- [3A9Z] Anaemias or other erythrocyte disorders, unspecified --PARENT--> [?] Anaemias or other erythrocyte disorders --CHILD--> [?] Nutritional or metabolic anaemias --- Walk 2 --- [3A9Z] Anaemias or other erythrocyte disorders, unspecified --PARENT--> [?] Anaemias or other erythrocyte disorders --RELATED_TO--> [?] Anaemia complicating pregnancy, childbirth or the puerperium Def: A condition of the circulatory system affecting pregnant females, characterised by a haemoglobin level below 11 grams per decilitre that complicates pregnancy, childbirth, or the puerperium.... --- Walk 3 --- [KA8Y] Other specified haemorrhagic or haematological disorders of fetus or newborn --PARENT--> [?] Haemorrhagic or haematological disorders of fetus or newborn Def: A group of conditions occurring during the period of time around childbirth, especially the five months before and one month after birth which are associated with bleeding, the blood, and blood formin... --EXCLUDES--> [?] Congenital stenosis or stricture of bile ducts --- Walk 4 --- [KA8Y] Other specified haemorrhagic or haematological disorders of fetus or newborn --PARENT--> [?] Haemorrhagic or haematological disorders of fetus or newborn Def: A group of conditions occurring during the period of time around childbirth, especially the five months before and one month after birth which are associated with bleeding, the blood, and blood formin... --EXCLUDES--> [?] Hereditary haemolytic anaemia --- Walk 5 --- [3A70.11] Aplastic anaemia due to other external agents --PARENT--> [3A70.1] Acquired aplastic anaemias Def: A condition occurring secondary to other disorders or via an auto-immune response directed to the bone marrow arising after birth. This disease is characterised by an almost complete absence of hemato... --RELATED_TO--> [?] Myelofibrosis with myeloid metaplasia Def: Myelofibrosis with myeloid metaplasia is a myeloproliferative disease which clinical manifestations depend on the type of blood cell affected and may include anaemia, pallor, splenomegaly, hypermetabo... --- Walk 6 --- [3A70.11] Aplastic anaemia due to other external agents --PARENT--> [3A70.1] Acquired aplastic anaemias Def: A condition occurring secondary to other disorders or via an auto-immune response directed to the bone marrow arising after birth. This disease is characterised by an almost complete absence of hemato... --CHILD--> [3A70.10] Drug-induced aplastic anaemia Def: A disease caused by drug intake. This disease is characterised by inability of stem cells to generate new mature cells leading to low levels of red blood cells, white blood cells, platelets. This dise...
[ "[3A9Z] Anaemias or other erythrocyte disorders, unspecified\n --PARENT--> [?] Anaemias or other erythrocyte disorders\n --CHILD--> [?] Nutritional or metabolic anaemias", "[3A9Z] Anaemias or other erythrocyte disorders, unspecified\n --PARENT--> [?] Anaemias or other erythrocyte disorders\n --RELATED_TO--> [?] Anaemia complicating pregnancy, childbirth or the puerperium\n Def: A condition of the circulatory system affecting pregnant females, characterised by a haemoglobin level below 11 grams per decilitre that complicates pregnancy, childbirth, or the puerperium....", "[KA8Y] Other specified haemorrhagic or haematological disorders of fetus or newborn\n --PARENT--> [?] Haemorrhagic or haematological disorders of fetus or newborn\n Def: A group of conditions occurring during the period of time around childbirth, especially the five months before and one month after birth which are associated with bleeding, the blood, and blood formin...\n --EXCLUDES--> [?] Congenital stenosis or stricture of bile ducts", "[KA8Y] Other specified haemorrhagic or haematological disorders of fetus or newborn\n --PARENT--> [?] Haemorrhagic or haematological disorders of fetus or newborn\n Def: A group of conditions occurring during the period of time around childbirth, especially the five months before and one month after birth which are associated with bleeding, the blood, and blood formin...\n --EXCLUDES--> [?] Hereditary haemolytic anaemia", "[3A70.11] Aplastic anaemia due to other external agents\n --PARENT--> [3A70.1] Acquired aplastic anaemias\n Def: A condition occurring secondary to other disorders or via an auto-immune response directed to the bone marrow arising after birth. This disease is characterised by an almost complete absence of hemato...\n --RELATED_TO--> [?] Myelofibrosis with myeloid metaplasia\n Def: Myelofibrosis with myeloid metaplasia is a myeloproliferative disease which clinical manifestations depend on the type of blood cell affected and may include anaemia, pallor, splenomegaly, hypermetabo...", "[3A70.11] Aplastic anaemia due to other external agents\n --PARENT--> [3A70.1] Acquired aplastic anaemias\n Def: A condition occurring secondary to other disorders or via an auto-immune response directed to the bone marrow arising after birth. This disease is characterised by an almost complete absence of hemato...\n --CHILD--> [3A70.10] Drug-induced aplastic anaemia\n Def: A disease caused by drug intake. This disease is characterised by inability of stem cells to generate new mature cells leading to low levels of red blood cells, white blood cells, platelets. This dise..." ]
3A9Z
Anaemias or other erythrocyte disorders, unspecified
[ { "from_icd11": "3A9Z", "icd10_code": "D6489", "icd10_title": "Other specified anemias" }, { "from_icd11": "3A9Z", "icd10_code": "D6481", "icd10_title": "Anemia due to antineoplastic chemotherapy" }, { "from_icd11": "3A9Z", "icd10_code": "D6101", "icd10_title": "Constitutional (pure) red blood cell aplasia" }, { "from_icd11": "3A9Z", "icd10_code": "D6109", "icd10_title": "Other constitutional aplastic anemia" }, { "from_icd11": "3A9Z", "icd10_code": "D649", "icd10_title": "Anemia, unspecified" }, { "from_icd11": "3A9Z", "icd10_code": "D748", "icd10_title": "Other methemoglobinemias" }, { "from_icd11": "3A9Z", "icd10_code": "D749", "icd10_title": "Methemoglobinemia, unspecified" }, { "from_icd11": "3A9Z", "icd10_code": "D740", "icd10_title": "Congenital methemoglobinemia" }, { "from_icd11": "3A9Z", "icd10_code": "D60-D64", "icd10_title": "" }, { "from_icd11": "3A9Z", "icd10_code": "D64", "icd10_title": "Other anemias" }, { "from_icd11": "3A9Z", "icd10_code": "D74", "icd10_title": "Methemoglobinemia" }, { "from_icd11": "3A9Z", "icd10_code": "D55-D59", "icd10_title": "" }, { "from_icd11": "3A9Z", "icd10_code": "D610", "icd10_title": "Constitutional aplastic anemia" }, { "from_icd11": "3A9Z", "icd10_code": "D648", "icd10_title": "Other specified anemias" }, { "from_icd11": "3A70.11", "icd10_code": "D612", "icd10_title": "Aplastic anemia due to other external agents" } ]
D6489
Other specified anemias
A 30-year-old female was admitted to our hospital after an elevated carbohydrate antigen (CA 19-9, 42.1 U/ml) was discovered on a health check-up. Her past medical history was unremarkable. Contrast-enhanced computed tomography (CT) was performed to check for abdominal malignancy. Axial and coronal reformatted arterial phase CT images showed an 8 cm, avidly heterogeneous enhancing mass (arrow) below the left kidney (open arrow). Left hydronephrosis (open arrow) occurred as the mass (arrow) compressed the left upper ureter. Coronal maximum-intensity projection reformatted CT image revealed multiple serpentine arteries (open arrowheads) along the periphery of the mass (arrow). The patient underwent magnetic resonance imaging (MRI) for further evaluation. The retroperitoneal mass (arrow) was iso-intense on T1-weighted image and hyperintense on T2-weighted image, with a well-circumscribed margin . Coronal T2-weighted image revealed multiple signal voids (open arrowheads) along the periphery of the mass (arrow), a finding that suggests the vessels . Axial dynamic gadolinium-enhanced T1-weighted images demonstrated the mass (arrow) with heterogeneous and strong enhancement on the arterial phase and prolonged enhancement on the portal venous and three-minute delayed phase . The patient underwent mass excision and left nephrectomy, and she was diagnosed with retroperitoneal solitary fibrous tumor (SFT).
3.898438
0.981934
sec[0]/p[0]
en
0.999995
32676545
https://doi.org/10.5334/jbsr.2150
[ "arrow", "open", "weighted", "coronal", "phase", "check", "enhanced", "axial", "reformatted", "arterial" ]
[ { "code": "DA0E.5Y", "title": "Other specified malocclusion" }, { "code": "ME05.0", "title": "Constipation" }, { "code": "QB61.Z", "title": "Presence of artificial opening, unspecified" }, { "code": "LA8B.4", "title": "Patent arterial duct" }, { "code": "NA81.4", "title": "Open bite of thorax" }, { "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" }, { "code": "JA65.2", "title": "Excessive weight gain in pregnancy" } ]
=== ICD-11 CODES FOUND === [DA0E.5Y] Other specified malocclusion Also known as: Other specified malocclusion | Crossbite | overbite | openbite | excessive overbite Includes: Crossbite [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 [QB61.Z] Presence of artificial opening, unspecified Also known as: Presence of artificial opening, unspecified | Presence of artificial opening | artificial opening status | Artificial opening status, unspecified [LA8B.4] Patent arterial duct Definition: A congenital cardiovascular finding in which the arterial duct (ductus arteriosus) is open beyond the normal age of spontaneous closure. Also known as: Patent arterial duct | patent ductus Botalli | patent ductus arteriosus NOS | open ductus arteriosus | persistent ductus arteriosus Includes: bilateral arterial ducts [NA81.4] Open bite of thorax Also known as: Open bite of thorax | Open bite of front wall of thorax | Open bite of back wall of thorax [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 [JA65.2] Excessive weight gain in pregnancy Definition: Any reason for encounter to assess (or care for) a mother for excessive weight gain during pregnancy. Also known as: Excessive weight gain in pregnancy | excessive weight gain in pregnancy, unspecified trimester | maternal obesity syndrome | maternal obesity without hypertension | abnormal weight gain in pregnancy Excludes: Gestational oedema without hypertension === GRAPH WALKS === --- Walk 1 --- [DA0E.5Y] Other specified malocclusion --PARENT--> [DA0E.5] Malocclusion Def: Malocclusion is the atypical relationship between maxillary and mandibular teeth which may interfere with the efficiency of excursive movements of the mandible that are essential for the effective mas... --PARENT--> [DA0E] Dentofacial anomalies Def: A congenital or acquired abnormality in which the dental and oral structures deviate from normal form, function, or position.... --- Walk 2 --- [DA0E.5Y] Other specified malocclusion --PARENT--> [DA0E.5] Malocclusion Def: Malocclusion is the atypical relationship between maxillary and mandibular teeth which may interfere with the efficiency of excursive movements of the mandible that are essential for the effective mas... --CHILD--> [DA0E.51] Angle class I malocclusion Def: The maxillary first permanent molar is in slight distoversion in relation to the mandibular first permanent molar, and the mesiobuccal cusp of the maxillary molar is aligned with the buccal groove of ... --- Walk 3 --- [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 Def: Functional constipation is a functional bowel disorder that presents as persistently difficult, infrequent, or seemingly incomplete defecation, which do not meet IBS criteria.... --CHILD--> [?] 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... --- Walk 4 --- [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 5 --- [QB61.Z] Presence of artificial opening, unspecified --PARENT--> [QB61] Presence of artificial opening --EXCLUDES--> [?] Malfunction or complication of external stoma of urinary tract Def: A condition caused by a surgically created opening connecting the urinary tract to the external environment. This condition is characterised by dysfunction or decreased function of the incision.... --- Walk 6 --- [QB61.Z] Presence of artificial opening, unspecified --PARENT--> [QB61] Presence of artificial opening --EXCLUDES--> [?] Malfunction or complication of external stoma of urinary tract Def: A condition caused by a surgically created opening connecting the urinary tract to the external environment. This condition is characterised by dysfunction or decreased function of the incision....
[ "[DA0E.5Y] Other specified malocclusion\n --PARENT--> [DA0E.5] Malocclusion\n Def: Malocclusion is the atypical relationship between maxillary and mandibular teeth which may interfere with the efficiency of excursive movements of the mandible that are essential for the effective mas...\n --PARENT--> [DA0E] Dentofacial anomalies\n Def: A congenital or acquired abnormality in which the dental and oral structures deviate from normal form, function, or position....", "[DA0E.5Y] Other specified malocclusion\n --PARENT--> [DA0E.5] Malocclusion\n Def: Malocclusion is the atypical relationship between maxillary and mandibular teeth which may interfere with the efficiency of excursive movements of the mandible that are essential for the effective mas...\n --CHILD--> [DA0E.51] Angle class I malocclusion\n Def: The maxillary first permanent molar is in slight distoversion in relation to the mandibular first permanent molar, and the mesiobuccal cusp of the maxillary molar is aligned with the buccal groove of ...", "[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\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 --CHILD--> [?] 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...", "[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....", "[QB61.Z] Presence of artificial opening, unspecified\n --PARENT--> [QB61] Presence of artificial opening\n --EXCLUDES--> [?] Malfunction or complication of external stoma of urinary tract\n Def: A condition caused by a surgically created opening connecting the urinary tract to the external environment. This condition is characterised by dysfunction or decreased function of the incision....", "[QB61.Z] Presence of artificial opening, unspecified\n --PARENT--> [QB61] Presence of artificial opening\n --EXCLUDES--> [?] Malfunction or complication of external stoma of urinary tract\n Def: A condition caused by a surgically created opening connecting the urinary tract to the external environment. This condition is characterised by dysfunction or decreased function of the incision...." ]
DA0E.5Y
Other specified malocclusion
[ { "from_icd11": "ME05.0", "icd10_code": "K5900", "icd10_title": "Constipation, unspecified" }, { "from_icd11": "ME05.0", "icd10_code": "K5909", "icd10_title": "Other constipation" }, { "from_icd11": "QB61.Z", "icd10_code": "Z936", "icd10_title": "Other artificial openings of urinary tract status" }, { "from_icd11": "QB61.Z", "icd10_code": "Z934", "icd10_title": "Other artificial openings of gastrointestinal tract status" }, { "from_icd11": "QB61.Z", "icd10_code": "Z938", "icd10_title": "Other artificial opening status" }, { "from_icd11": "QB61.Z", "icd10_code": "Z939", "icd10_title": "Artificial opening status, unspecified" }, { "from_icd11": "QB61.Z", "icd10_code": "Z93", "icd10_title": "Artificial opening status" }, { "from_icd11": "LA8B.4", "icd10_code": "Q250", "icd10_title": "Patent ductus arteriosus" }, { "from_icd11": "MG43.5", "icd10_code": "R634", "icd10_title": "Abnormal weight loss" }, { "from_icd11": "MG43.6", "icd10_code": "R635", "icd10_title": "Abnormal weight gain" }, { "from_icd11": "5B80.0Z", "icd10_code": "E669", "icd10_title": "Obesity, unspecified" }, { "from_icd11": "JA65.2", "icd10_code": "O2603", "icd10_title": "Excessive weight gain in pregnancy, third trimester" }, { "from_icd11": "JA65.2", "icd10_code": "O2601", "icd10_title": "Excessive weight gain in pregnancy, first trimester" }, { "from_icd11": "JA65.2", "icd10_code": "O2602", "icd10_title": "Excessive weight gain in pregnancy, second trimester" }, { "from_icd11": "JA65.2", "icd10_code": "O260", "icd10_title": "Excessive weight gain in pregnancy" } ]
K5900
Constipation, unspecified
Patient 1 : A 21-year-old otherwise healthy female was diagnosed with core-binding factor (CBF)-AML (t (8; 12) (q21.3; q22)), corresponding RUNX1/RUNX1T1 transcript. After the first-line therapies ( Table 1 ), minimal residual disease (MRD) positivity of 0.02% was still detected in the bone marrow (BM). The patient then moved to Finland. At the first visit to our center, a florid BM-relapse was detected only 14 weeks after the start of the last consolidation cycle. We initiated a course of 7 + 3 combined with fractionated GO ( Table 1 ). Along with stomatitis and cytarabine-related cutaneous reaction, from day 13 onwards, the patient suffered from high fever, malaise, Clostridium difficile colitis, and oral HSV infection. Moreover, Enterococcus faecium septicemia persisted from day 21, though no deep foci of infection or endocarditis were detected. Human herpes virus 6 nucleic acid test (HHV6-NAT) was positive on day 25 . As a first sign of a toxic reaction, plasma lactate dehydrogenase (P-LD) started to rise from day 11. The reaction escalated quickly from day 19, when blood samples became macroscopically hemolytic. Free plasma hemoglobin (P-Hb) rose markedly, but P-haptoglobin (P-Haptog) and P-Bilirubin (P-Bil) were paradoxically normal, unlike in typical intravascular hemolysis . Kidney and liver tests remained normal, but plasma troponin I level was elevated and the patient was hypertensive.
4.078125
0.972168
sec[1]/p[0]
en
0.999997
33824768
https://doi.org/10.1155/2021/6641349
[ "reaction", "plasma", "infection", "otherwise", "healthy", "diagnosed", "core", "binding", "factor", "corresponding" ]
[ { "code": "NE60", "title": "Harmful effects of drugs, medicaments or biological substances, not elsewhere classified" }, { "code": "6B43", "title": "Adjustment disorder" }, { "code": "NE80.Z", "title": "Injury or harm arising following infusion, transfusion or therapeutic injection, not elsewhere classified, unspecified" }, { "code": "4B24.Z", "title": "Graft-versus-host disease, unspecified" }, { "code": "NE80.3", "title": "Other serum reactions" }, { "code": "2A83.2", "title": "Solitary plasmacytoma" }, { "code": "2A83.Z", "title": "Plasma cell neoplasm, unspecified" }, { "code": "5D0Y", "title": "Other specified metabolic disorders" }, { "code": "2A83.Y", "title": "Other specified plasma cell neoplasms" }, { "code": "2A83.4", "title": "Plasma cell leukaemia" } ]
=== 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 [6B43] Adjustment disorder Definition: Adjustment disorder is a maladaptive reaction to an identifiable psychosocial stressor or multiple stressors (e.g. divorce, illness or disability, socio-economic problems, conflicts at home or work) that usually emerges within a month of the stressor. The disorder is characterised by preoccupation with the stressor or its consequences, including excessive worry, recurrent and distressing thoughts about the stressor, or constant rumination about its implications, as well as by failure to adapt to Also known as: Adjustment disorder | brief situational non-psychotic disorder | adaptation reaction NOS | adjustment reaction | emotional crisis Excludes: separation anxiety disorder of childhood | Recurrent depressive disorder | Single episode depressive disorder [NE80.Z] Injury or harm arising following infusion, transfusion or therapeutic injection, not elsewhere classified, unspecified Also known as: Injury or harm arising following infusion, transfusion or therapeutic injection, not elsewhere classified, unspecified | Injury or harm arising following infusion, transfusion or therapeutic injection, not elsewhere classified | transfusion reaction NOS | Blood transfusion reaction not elsewhere classified | blood transfusion reaction NOS [4B24.Z] Graft-versus-host disease, unspecified Also known as: Graft-versus-host disease, unspecified | Graft-versus-host disease | GVHD - [graft-versus-host disease] | graft-versus-host reaction or disease | GVH - [graft-versus-host] disease [NE80.3] Other serum reactions Also known as: Other serum reactions | Allergic reaction to serum | serum allergy | Complications of vaccination, protein sickness | Protein sickness Excludes: serum hepatitis [2A83.2] Solitary plasmacytoma Definition: A single focus of clonal (malignant) plasma cells either in the bone or in another anatomic site without peripheral blood involvement. Also known as: Solitary plasmacytoma | solitary plasmacytoma without mention of remission | solitary myeloma | localised malignant plasma cell tumour NOS | plasmacytoma NOS Includes: solitary myeloma [2A83.Z] Plasma cell neoplasm, unspecified Also known as: Plasma cell neoplasm, unspecified | Plasma cell neoplasms | plasma cell tumours | plasma cells dyscrasia | plasma cell neoplasm NOS [5D0Y] Other specified metabolic disorders Also known as: Other specified metabolic disorders | Disorders of plasma-protein metabolism, not elsewhere classified | abnormal protein transport | dysproteinaemia | Absence of albumin in blood [2A83.Y] Other specified plasma cell neoplasms Also known as: Other specified plasma cell neoplasms | POEMS syndrome | Osteosclerotic myeloma | Peripheral neuropathy - organomegaly - endocrinopathy - monoclonal plasma cell disorder - skin changes [2A83.4] Plasma cell leukaemia Definition: An aggressive plasma cell neoplasm. It is characterised by the presence of neoplastic plasma cells in the peripheral blood (PB). The neoplastic plasma cells comprise more than 20% of the white cells in the PB or the number of clonal plasma cells in the PB exceeds 2x10⁹/L. Also known as: Plasma cell leukaemia | plasma cell leukaemia, NOS | leukemic plasma cell | plasma cell leukaemia without mention of remission | plasmacytic leukaemia === GRAPH WALKS === --- Walk 1 --- [NE60] Harmful effects of drugs, medicaments or biological substances, not elsewhere classified --PARENT--> [?] Harmful effects of substances --CHILD--> [NE6Z] Harmful effects of unspecified substance --- 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 --- [6B43] Adjustment disorder Def: Adjustment disorder is a maladaptive reaction to an identifiable psychosocial stressor or multiple stressors (e.g. divorce, illness or disability, socio-economic problems, conflicts at home or work) t... --EXCLUDES--> [?] Separation anxiety disorder Def: Separation anxiety disorder is characterised by marked and excessive fear or anxiety about separation from specific attachment figures. In children and adolescents, separation anxiety typically focuse... --EXCLUDES--> [?] Social anxiety disorder Def: Social anxiety disorder is characterised by marked and excessive fear or anxiety that consistently occurs in one or more social situations such as social interactions (e.g. having a conversation), doi... --- Walk 4 --- [6B43] Adjustment disorder Def: Adjustment disorder is a maladaptive reaction to an identifiable psychosocial stressor or multiple stressors (e.g. divorce, illness or disability, socio-economic problems, conflicts at home or work) t... --EXCLUDES--> [?] Single episode depressive disorder Def: Single episode depressive disorder is characterised by the presence or history of one depressive episode when there is no history of prior depressive episodes. A depressive episode is characterised by... --EXCLUDES--> [?] Recurrent depressive disorder Def: Recurrent depressive disorder is characterised by a history of at least two depressive episodes separated by at least several months without significant mood disturbance. A depressive episode is chara... --- Walk 5 --- [NE80.Z] Injury or harm arising following infusion, transfusion or therapeutic injection, not elsewhere classified, unspecified --PARENT--> [NE80] Injury or harm arising following infusion, transfusion or therapeutic injection, not elsewhere classified --EXCLUDES--> [?] Endophthalmitis --- Walk 6 --- [NE80.Z] Injury or harm arising following infusion, transfusion or therapeutic injection, not elsewhere classified, unspecified --PARENT--> [NE80] Injury or harm arising following infusion, transfusion or therapeutic injection, not elsewhere classified --EXCLUDES--> [?] Failure or rejection of transplanted organs or tissues
[ "[NE60] Harmful effects of drugs, medicaments or biological substances, not elsewhere classified\n --PARENT--> [?] Harmful effects of substances\n --CHILD--> [NE6Z] Harmful effects of unspecified substance", "[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 ...", "[6B43] Adjustment disorder\n Def: Adjustment disorder is a maladaptive reaction to an identifiable psychosocial stressor or multiple stressors (e.g. divorce, illness or disability, socio-economic problems, conflicts at home or work) t...\n --EXCLUDES--> [?] Separation anxiety disorder\n Def: Separation anxiety disorder is characterised by marked and excessive fear or anxiety about separation from specific attachment figures. In children and adolescents, separation anxiety typically focuse...\n --EXCLUDES--> [?] Social anxiety disorder\n Def: Social anxiety disorder is characterised by marked and excessive fear or anxiety that consistently occurs in one or more social situations such as social interactions (e.g. having a conversation), doi...", "[6B43] Adjustment disorder\n Def: Adjustment disorder is a maladaptive reaction to an identifiable psychosocial stressor or multiple stressors (e.g. divorce, illness or disability, socio-economic problems, conflicts at home or work) t...\n --EXCLUDES--> [?] Single episode depressive disorder\n Def: Single episode depressive disorder is characterised by the presence or history of one depressive episode when there is no history of prior depressive episodes. A depressive episode is characterised by...\n --EXCLUDES--> [?] Recurrent depressive disorder\n Def: Recurrent depressive disorder is characterised by a history of at least two depressive episodes separated by at least several months without significant mood disturbance. A depressive episode is chara...", "[NE80.Z] Injury or harm arising following infusion, transfusion or therapeutic injection, not elsewhere classified, unspecified\n --PARENT--> [NE80] Injury or harm arising following infusion, transfusion or therapeutic injection, not elsewhere classified\n --EXCLUDES--> [?] Endophthalmitis", "[NE80.Z] Injury or harm arising following infusion, transfusion or therapeutic injection, not elsewhere classified, unspecified\n --PARENT--> [NE80] Injury or harm arising following infusion, transfusion or therapeutic injection, not elsewhere classified\n --EXCLUDES--> [?] Failure or rejection of transplanted organs or tissues" ]
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 patient was a 16-year-old male (CMV seronegative at the time of transplant) who underwent liver transplantation for Primary Sclerosing Cholangitis from a 4/6 HLA-matched deceased and unrelated donor (CMV seropositive). Twenty-one days after the transplantation, the patient developed a symptomatic primary CMV infection (CMV-DNA 1,686,000 copies/mL) characterized by leukopenia (760 cells/μL) and interstitial pneumonia. After 20 days-therapy with GCV followed by one month with Valganciclovir (900 mg × 2 vv/day), CMV viral load decreased but a severe absolute leukopenia persisted . Two weeks later, the infection recurred (CMV DNA 193,300 copies/mL) with manifestation of alveolar pneumonitis associated with a worsening of the clinical status (weight lost and sleeping status). The patient was treated with Valganciclovir, 900 mg × 2 vv/day, resulting in a decrease of CMV DNAemia. One month later, another increase of CMV-DNA (116,829 copies/mL) was observed and a third cycle (one month) of antiviral therapy was started and associated with the reduction of immunosuppression with Tacrolimus. CMV-DNA viral load decreased, but the status of severe leukopenia (760 cells/μL) and thrombocytopenia (126,000 platelet/mm 3 ) persisted. Despite immunosuppression reduction. No circulating IFN-γ secreting CMV-specific T-cells were detected in the blood. CMV-DNA was also detected in a sample of bone marrow biopsy.
4.105469
0.973145
sec[0]/sec[0]/p[0]
en
0.999997
33810329
https://doi.org/10.3390/microorganisms9040684
[ "copies", "leukopenia", "cells", "status", "transplantation", "infection", "valganciclovir", "viral", "load", "persisted" ]
[ { "code": "MA16.10", "title": "Decreased white blood cell count" }, { "code": "4A01.10", "title": "Severe combined immunodeficiencies" }, { "code": "FA20.0", "title": "Seropositive rheumatoid arthritis" }, { "code": "4B00.00", "title": "Constitutional neutropaenia" }, { "code": "MF9Y", "title": "Other specified clinical findings on examination of urine, without diagnosis" }, { "code": "5C56.20", "title": "Mucolipidosis" }, { "code": "3A51.1", "title": "Sickle cell disease without crisis" }, { "code": "9A96.3", "title": "Primary anterior uveitis" }, { "code": "3A61.Z", "title": "Acquired pure red cell aplasia, unspecified" }, { "code": "8A66.1Z", "title": "Non-convulsive status epilepticus, unspecified" } ]
=== ICD-11 CODES FOUND === [MA16.10] Decreased white blood cell count Also known as: Decreased white blood cell count | low white cell count | leukopenia | low white blood cell count | hypoleukocytosis (deprecated) [4A01.10] Severe combined immunodeficiencies Definition: Severe combined immunodeficiency (SCID) comprises a group of rare monogenic primary immunodeficiency disorders characterised by a lack of functional peripheral T lymphocytes resulting in early-onset severe respiratory infections and failure to thrive. Also known as: Severe combined immunodeficiencies | SCID - [Severe combined immunodeficiencies] | severe combined immunodeficiency disease | Severe combined immunodeficiency with reticular dysgenesis | Severe combined immunodeficiency with leukopenia [FA20.0] Seropositive rheumatoid arthritis Also known as: Seropositive rheumatoid arthritis | high positive rheumatoid factor | low positive rheumatoid factor | high positive anticitrullinated protein antibody | low positive anticitrullinated protein antibody [4B00.00] Constitutional neutropaenia Definition: This is a granulocyte disorder characterised by an abnormally low number of neutrophils. Neutrophils usually make up 50-70% of circulating white blood cells and serve as the primary defence against infections by destroying bacteria in the blood. Also known as: Constitutional neutropaenia | congenital agranulocytosis and neutropaenia | congenital leukopaenia | Congenital neutropaenias | primary neutropaenia Excludes: Cartilage-hair hypoplasia [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) [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] [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 [8A66.1Z] Non-convulsive status epilepticus, unspecified Also known as: Non-convulsive status epilepticus, unspecified | Non-convulsive status epilepticus | Epileptic absence status | Petit mal status epilepticus | Petit-mal status === GRAPH WALKS === --- Walk 1 --- [MA16.10] Decreased white blood cell count --PARENT--> [MA16.1] Abnormality of white blood cells --EXCLUDES--> [?] Neutrophilia --- Walk 2 --- [MA16.10] Decreased white blood cell count --PARENT--> [MA16.1] Abnormality of white blood cells --EXCLUDES--> [?] Neutrophilia --- Walk 3 --- [4A01.10] Severe combined immunodeficiencies Def: Severe combined immunodeficiency (SCID) comprises a group of rare monogenic primary immunodeficiency disorders characterised by a lack of functional peripheral T lymphocytes resulting in early-onset s... --PARENT--> [4A01.1] Combined immunodeficiencies --RELATED_TO--> [?] Laron syndrome with immunodeficiency Def: Laron syndrome with immunodeficiency is characterised by severe post-natal growth retardation, delayed bone age and facial dysmorphism (prominent forehead, hypoplastic nasal bridge), and low serum IGF... --- Walk 4 --- [4A01.10] Severe combined immunodeficiencies Def: Severe combined immunodeficiency (SCID) comprises a group of rare monogenic primary immunodeficiency disorders characterised by a lack of functional peripheral T lymphocytes resulting in early-onset s... --PARENT--> [4A01.1] Combined immunodeficiencies --CHILD--> [4A01.12] Major histocompatibility complex class II deficiency Def: Immunodeficiency by defective expression of HLA class II is an autosomal recessive primary immune deficiency, manifesting by recurrent viral and bacterial infections, often leading to chronic diarrhoe... --- Walk 5 --- [FA20.0] Seropositive rheumatoid arthritis --PARENT--> [FA20] Rheumatoid arthritis Def: Rheumatoid arthritis (RA) is persistent and/or erosive disease that is defined as the confirmed presence of synovitis in at least 1 joint, absence of an alternative diagnosis that better explains the ... --RELATED_TO--> [?] Respiratory disorders in rheumatoid arthritis Def: This encompasses pathological conditions affecting the organs and tissues that make gas exchange possible in higher organisms, and includes conditions of the upper respiratory tract, trachea, bronchi,... --- Walk 6 --- [FA20.0] Seropositive rheumatoid arthritis --PARENT--> [FA20] Rheumatoid arthritis Def: Rheumatoid arthritis (RA) is persistent and/or erosive disease that is defined as the confirmed presence of synovitis in at least 1 joint, absence of an alternative diagnosis that better explains the ... --EXCLUDES--> [?] Juvenile idiopathic polyarthritis, rheumatoid factor negative Def: Rheumatoid factor-negative polyarthritis is a term used to describe a group of poorly defined heterogenous conditions that incorporates forms of rheumatoid factor-negative polyarthritis and forms of o...
[ "[MA16.10] Decreased white blood cell count\n --PARENT--> [MA16.1] Abnormality of white blood cells\n --EXCLUDES--> [?] Neutrophilia", "[MA16.10] Decreased white blood cell count\n --PARENT--> [MA16.1] Abnormality of white blood cells\n --EXCLUDES--> [?] Neutrophilia", "[4A01.10] Severe combined immunodeficiencies\n Def: Severe combined immunodeficiency (SCID) comprises a group of rare monogenic primary immunodeficiency disorders characterised by a lack of functional peripheral T lymphocytes resulting in early-onset s...\n --PARENT--> [4A01.1] Combined immunodeficiencies\n --RELATED_TO--> [?] Laron syndrome with immunodeficiency\n Def: Laron syndrome with immunodeficiency is characterised by severe post-natal growth retardation, delayed bone age and facial dysmorphism (prominent forehead, hypoplastic nasal bridge), and low serum IGF...", "[4A01.10] Severe combined immunodeficiencies\n Def: Severe combined immunodeficiency (SCID) comprises a group of rare monogenic primary immunodeficiency disorders characterised by a lack of functional peripheral T lymphocytes resulting in early-onset s...\n --PARENT--> [4A01.1] Combined immunodeficiencies\n --CHILD--> [4A01.12] Major histocompatibility complex class II deficiency\n Def: Immunodeficiency by defective expression of HLA class II is an autosomal recessive primary immune deficiency, manifesting by recurrent viral and bacterial infections, often leading to chronic diarrhoe...", "[FA20.0] Seropositive rheumatoid arthritis\n --PARENT--> [FA20] Rheumatoid arthritis\n Def: Rheumatoid arthritis (RA) is persistent and/or erosive disease that is defined as the confirmed presence of synovitis in at least 1 joint, absence of an alternative diagnosis that better explains the ...\n --RELATED_TO--> [?] Respiratory disorders in rheumatoid arthritis\n Def: This encompasses pathological conditions affecting the organs and tissues that make gas exchange possible in higher organisms, and includes conditions of the upper respiratory tract, trachea, bronchi,...", "[FA20.0] Seropositive rheumatoid arthritis\n --PARENT--> [FA20] Rheumatoid arthritis\n Def: Rheumatoid arthritis (RA) is persistent and/or erosive disease that is defined as the confirmed presence of synovitis in at least 1 joint, absence of an alternative diagnosis that better explains the ...\n --EXCLUDES--> [?] Juvenile idiopathic polyarthritis, rheumatoid factor negative\n Def: Rheumatoid factor-negative polyarthritis is a term used to describe a group of poorly defined heterogenous conditions that incorporates forms of rheumatoid factor-negative polyarthritis and forms of o..." ]
MA16.10
Decreased white blood cell count
[ { "from_icd11": "4A01.10", "icd10_code": "D810", "icd10_title": "Severe combined immunodeficiency [SCID] with reticular dysgenesis" }, { "from_icd11": "4A01.10", "icd10_code": "D811", "icd10_title": "Severe combined immunodeficiency [SCID] with low T- and B-cell numbers" }, { "from_icd11": "4A01.10", "icd10_code": "D812", "icd10_title": "Severe combined immunodeficiency [SCID] with low or normal B-cell numbers" }, { "from_icd11": "4A01.10", "icd10_code": "D813", "icd10_title": "Adenosine deaminase [ADA] deficiency" }, { "from_icd11": "4A01.10", "icd10_code": "D822", "icd10_title": "Immunodeficiency with short-limbed stature" }, { "from_icd11": "FA20.0", "icd10_code": "M0569", "icd10_title": "Rheumatoid arthritis of multiple sites with involvement of other organs and systems" }, { "from_icd11": "FA20.0", "icd10_code": "M0579", "icd10_title": "Rheumatoid arthritis with rheumatoid factor of multiple sites without organ or systems involvement" }, { "from_icd11": "FA20.0", "icd10_code": "M05612", "icd10_title": "Rheumatoid arthritis of left shoulder with involvement of other organs and systems" }, { "from_icd11": "FA20.0", "icd10_code": "M0570", "icd10_title": "Rheumatoid arthritis with rheumatoid factor of unspecified site without organ or systems involvement" }, { "from_icd11": "FA20.0", "icd10_code": "M0560", "icd10_title": "Rheumatoid arthritis of unspecified site with involvement of other organs and systems" }, { "from_icd11": "FA20.0", "icd10_code": "M0500", "icd10_title": "Felty's syndrome, unspecified site" }, { "from_icd11": "FA20.0", "icd10_code": "M0639", "icd10_title": "Rheumatoid nodule, multiple sites" }, { "from_icd11": "FA20.0", "icd10_code": "M0630", "icd10_title": "Rheumatoid nodule, unspecified site" }, { "from_icd11": "FA20.0", "icd10_code": "M05", "icd10_title": "Rheumatoid arthritis with rheumatoid factor" }, { "from_icd11": "FA20.0", "icd10_code": "M050", "icd10_title": "Felty's syndrome" } ]
D810
Severe combined immunodeficiency [SCID] with reticular dysgenesis
The patient continued to be followed on an approximately yearly basis for several years. By age 19, his scotopic ffERG had become mildly decreased, accompanied by continued worsening of photopic signals (mild to moderate). Bright flash responses were not electronegative. A corneal specialist consultation found he was not a good candidate for surgical intervention. At age 21, he was incidentally noted to have developed bilateral retinoschisis on Cirrus OCT, with schisis mostly in the outer plexiform layer . Acuity was reduced to 20/63 OD and 20/125 OS, which was felt to be a real, significant change at the time. Although the cause was judged to be likely secondary to corneal edema, a contribution from schisis could not be excluded. Refraction at that time was −6.75 + 4.00×120 OD and −8.75 + 4.75×55 length data are not available, but neither fundoscopy nor OCT suggested a posterior staphyloma or other signs of myopic maculopathy. Although use of carbonic anhydrase inhibitor therapy was considered, it was not pursued due to continued corneal edema. Scans on subsequent follow-up over the past two years have shown approximately stable splitting. Although acuity remained stable in the left eye, it continued to drop in the right, last measuring 20/100 at age 23. In addition, mottling of blue-light autofluorescence signal was noted, particularly in the macula, consistent with his cone-rod degeneration .
4.050781
0.976563
sec[2]/p[4]
en
0.999998
32787478
https://doi.org/10.1080/13816810.2020.1799416
[ "corneal", "although", "approximately", "schisis", "acuity", "time", "edema", "yearly", "basis", "several" ]
[ { "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": "DA08.10", "title": "Excessive attrition of teeth" }, { "code": "9D94", "title": "Impairment of presenting visual acuity" }, { "code": "9D96", "title": "Impairment of uncorrected visual acuity" }, { "code": "9D95", "title": "Impairment of best corrected visual acuity" }, { "code": "PL13.52", "title": "Incorrect timing of drug or medicament, as mode of injury" } ]
=== 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 [DA08.10] Excessive attrition of teeth Definition: The pathological wearing away of tooth substance as a result of tooth-to-tooth contact. Also known as: Excessive attrition of teeth | occlusal wear of teeth | approximal wear of teeth [9D94] Impairment of presenting visual acuity Also known as: Impairment of presenting visual acuity [9D96] Impairment of uncorrected visual acuity Also known as: Impairment of uncorrected visual acuity [9D95] Impairment of best corrected visual acuity Also known as: Impairment of best corrected visual acuity [PL13.52] Incorrect timing of drug or medicament, as mode of injury Also known as: Incorrect timing of drug or medicament, as mode of injury | wrong timing of drug | timing error in giving drug | timing mistake in administration of drug | administration error involving timing of drug Excludes: Problem with delayed treatment | Overdose of substance, as mode of injury or harm === 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--> [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... --CHILD--> [?] Stromal keratitis Def: Herpes simplex (HSV) stromal keratitis is an infectious ocular disease of either necrotizing or non-necrotizing form, due to an HSV infection, and characterised by corneal stromal necrosis, inflammati... --- 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... --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 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--> [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", "[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 --CHILD--> [?] Stromal keratitis\n Def: Herpes simplex (HSV) stromal keratitis is an infectious ocular disease of either necrotizing or non-necrotizing form, due to an HSV infection, and characterised by corneal stromal necrosis, inflammati...", "[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...", "[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--> [9A71] Infectious keratitis" ]
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 patient also developed a fever and worsening cough. An auxiliary examination tested positive for mycoplasma pneumoniae, promping the addition of azithromycin therapy for infection control. Consequently, a chest Computer Tomography (CT) scan revealed a mass adjacent to the lower esophagus in the mediastinum, along with a small amount of pleural effusion on both sides . Further dynamic contrast-enhanced chest CT and mediastinal MRI were conducted, indicating a space-occupying lesion near the lower esophagus, suggesting a tumor-like lesion, potentially Castleman's disease. Taking into account the patient's history, clinical manifestations, and examination results, the girl was suspected to have Castleman's disease along with secondary pemphigus. Following a multidisciplinary team discussion, the patient received an endoscopic ultrasonography-guided fine needle aspiration that ruled out malignant tumors. Subsequently, she had video-assisted thoracoscopic surgery to remove the posterior mediastinal mass. The postoperative pathology revealed lymphoid hyperplasia, which is consistent with the hyaline-vascular type of Castleman's disease, based on the morphology, immunohistochemistry results, and molecular testing . However, the girl was in poor condition during the perioperative period , and her parents refused to conduct skin or mucosal biopsies to verify the diagnosis of paraneoplastic pemphigus.
3.927734
0.98291
sec[1]/sec[1]/p[3]
en
0.999995
PMC11620853
https://doi.org/10.3389/fped.2024.1469495
[ "castleman", "chest", "esophagus", "along", "mediastinal", "lesion", "girl", "pemphigus", "fever", "cough" ]
[ { "code": "4B2Y", "title": "Other specified disorders involving the immune system" }, { "code": "8E4A.1", "title": "Paraneoplastic or autoimmune disorders of the peripheral or autonomic nervous system" }, { "code": "2A81.Y", "title": "Other specified diffuse large B-cell lymphomas" }, { "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": "DA2Z", "title": "Diseases of oesophagus, unspecified" }, { "code": "DA24.Z", "title": "Oesophagitis, unspecified" } ]
=== ICD-11 CODES FOUND === [4B2Y] Other specified disorders involving the immune system Also known as: Other specified disorders involving the immune system | Certain inflammatory disorders with predominant lymph node involvement | Histiocytic necrotising lymphadenitis of Kikuchi and Fujimoto | Kikuchi-Fujimoto disease | Kimura disease [8E4A.1] Paraneoplastic or autoimmune disorders of the peripheral or autonomic nervous system Definition: Paraneoplastic and autoimmune disorders of the peripheral and autonomic nervous system result from a targeted immune attack on neurons or glial cells in the peripheral nervous systems (peripheral or autonomic neuropathies). 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 remains elusive though increasing e Also known as: Paraneoplastic or autoimmune disorders of the peripheral or autonomic nervous system | Paraneoplastic sensory ganglionopathy | Paraneoplastic sensory neuronopathy | Paraneoplastic sensory ganglionopathy, neural autoantibody negative | Autoimmune sensory ganglionopathy [2A81.Y] Other specified diffuse large B-cell lymphomas Also known as: Other specified diffuse large B-cell lymphomas | Diffuse large B-cell lymphoma of stomach | Large B-cell lymphoma arising in HHV8-associated multicentric Castleman disease | Richter syndrome [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 [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 === GRAPH WALKS === --- Walk 1 --- [4B2Y] Other specified disorders involving the immune system --PARENT--> [?] Certain disorders involving the immune system Def: Disorders in which disturbed immune regulation plays an important part but which cannot be more precisely located elsewhere in the classification.... --CHILD--> [4B22] Cryoglobulinaemia --- Walk 2 --- [4B2Y] Other specified disorders involving the immune system --PARENT--> [?] Certain disorders involving the immune system Def: Disorders in which disturbed immune regulation plays an important part but which cannot be more precisely located elsewhere in the classification.... --CHILD--> [4B21] Polyclonal hypergammaglobulinaemia --- Walk 3 --- [8E4A.1] Paraneoplastic or autoimmune disorders of the peripheral or autonomic nervous system Def: Paraneoplastic and autoimmune disorders of the peripheral and autonomic nervous system result from a targeted immune attack on neurons or glial cells in the peripheral nervous systems (peripheral or a... --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 4 --- [8E4A.1] Paraneoplastic or autoimmune disorders of the peripheral or autonomic nervous system Def: Paraneoplastic and autoimmune disorders of the peripheral and autonomic nervous system result from a targeted immune attack on neurons or glial cells in the peripheral nervous systems (peripheral or a... --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... --CHILD--> [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... --- Walk 5 --- [2A81.Y] Other specified diffuse large B-cell lymphomas --PARENT--> [2A81] Diffuse large B-cell lymphomas Def: Non-Hodgkin lymphomas are characterised by a proliferation of predominantly large neoplastic B lymphocytes.... --CHILD--> [2A81.0] Primary mediastinal large B-cell lymphoma Def: A large B-cell non-Hodgkin lymphoma arising in the mediastinum. Morphologically it is characterised by a massive diffuse lymphocytic proliferation associated with compartmentalizing fibrosis.... --- Walk 6 --- [2A81.Y] Other specified diffuse large B-cell lymphomas --PARENT--> [2A81] Diffuse large B-cell lymphomas Def: Non-Hodgkin lymphomas are characterised by a proliferation of predominantly large neoplastic B lymphocytes.... --CHILD--> [2A81.2] Plasmablastic lymphoma Def: An aggressive diffuse large B-cell lymphoma frequently arising in the setting of HIV infection and characterised by the presence of large neoplastic cells resembling B-immunoblasts which have the immu...
[ "[4B2Y] Other specified disorders involving the immune system\n --PARENT--> [?] Certain disorders involving the immune system\n Def: Disorders in which disturbed immune regulation plays an important part but which cannot be more precisely located elsewhere in the classification....\n --CHILD--> [4B22] Cryoglobulinaemia", "[4B2Y] Other specified disorders involving the immune system\n --PARENT--> [?] Certain disorders involving the immune system\n Def: Disorders in which disturbed immune regulation plays an important part but which cannot be more precisely located elsewhere in the classification....\n --CHILD--> [4B21] Polyclonal hypergammaglobulinaemia", "[8E4A.1] Paraneoplastic or autoimmune disorders of the peripheral or autonomic nervous system\n Def: Paraneoplastic and autoimmune disorders of the peripheral and autonomic nervous system result from a targeted immune attack on neurons or glial cells in the peripheral nervous systems (peripheral or a...\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.1] Paraneoplastic or autoimmune disorders of the peripheral or autonomic nervous system\n Def: Paraneoplastic and autoimmune disorders of the peripheral and autonomic nervous system result from a targeted immune attack on neurons or glial cells in the peripheral nervous systems (peripheral or a...\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 --CHILD--> [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...", "[2A81.Y] Other specified diffuse large B-cell lymphomas\n --PARENT--> [2A81] Diffuse large B-cell lymphomas\n Def: Non-Hodgkin lymphomas are characterised by a proliferation of predominantly large neoplastic B lymphocytes....\n --CHILD--> [2A81.0] Primary mediastinal large B-cell lymphoma\n Def: A large B-cell non-Hodgkin lymphoma arising in the mediastinum. Morphologically it is characterised by a massive diffuse lymphocytic proliferation associated with compartmentalizing fibrosis....", "[2A81.Y] Other specified diffuse large B-cell lymphomas\n --PARENT--> [2A81] Diffuse large B-cell lymphomas\n Def: Non-Hodgkin lymphomas are characterised by a proliferation of predominantly large neoplastic B lymphocytes....\n --CHILD--> [2A81.2] Plasmablastic lymphoma\n Def: An aggressive diffuse large B-cell lymphoma frequently arising in the setting of HIV infection and characterised by the presence of large neoplastic cells resembling B-immunoblasts which have the immu..." ]
4B2Y
Other specified disorders involving the immune system
[ { "from_icd11": "8E4A.1", "icd10_code": "M5489", "icd10_title": "Other dorsalgia" }, { "from_icd11": "8E4A.1", "icd10_code": "M5481", "icd10_title": "Occipital neuralgia" }, { "from_icd11": "8E4A.1", "icd10_code": "M5417", "icd10_title": "Radiculopathy, lumbosacral region" }, { "from_icd11": "8E4A.1", "icd10_code": "G0481", "icd10_title": "Other encephalitis and encephalomyelitis" }, { "from_icd11": "8E4A.1", "icd10_code": "M5414", "icd10_title": "Radiculopathy, thoracic region" }, { "from_icd11": "8E4A.1", "icd10_code": "G6289", "icd10_title": "Other specified polyneuropathies" }, { "from_icd11": "8E4A.1", "icd10_code": "M5418", "icd10_title": "Radiculopathy, sacral and sacrococcygeal region" }, { "from_icd11": "8E4A.1", "icd10_code": "M5415", "icd10_title": "Radiculopathy, thoracolumbar region" }, { "from_icd11": "8E4A.1", "icd10_code": "G6181", "icd10_title": "Chronic inflammatory demyelinating polyneuritis" }, { "from_icd11": "8E4A.1", "icd10_code": "M5410", "icd10_title": "Radiculopathy, site unspecified" }, { "from_icd11": "8E4A.1", "icd10_code": "G6281", "icd10_title": "Critical illness polyneuropathy" }, { "from_icd11": "8E4A.1", "icd10_code": "G6282", "icd10_title": "Radiation-induced polyneuropathy" }, { "from_icd11": "8E4A.1", "icd10_code": "G0489", "icd10_title": "Other myelitis" }, { "from_icd11": "8E4A.1", "icd10_code": "G6189", "icd10_title": "Other inflammatory polyneuropathies" }, { "from_icd11": "8E4A.1", "icd10_code": "M5413", "icd10_title": "Radiculopathy, cervicothoracic region" } ]
M5489
Other dorsalgia
With the horse in dorsal recumbency a standard midline approach was used, and a 25 cm incision was made through the linea alba. Manual exploration of the abdomen revealed a small intestinal strangulation, several dilated loops of small intestine and a mild impaction of the ascending colon. The strangulation was located in the distal jejunum , which after reduction and reposition appeared to have a Y-shaped anatomy in this horse . Given its appearance a congenital anomaly was presumed. The tube-like diverticulum originated from the mesenteric side of the jejunum instead of the anti-mesenteric side, as it is most often described for a Meckel’s diverticulum [ 9 – 11 ]. Oral to the strangulation, the jejunum was fluid filled and distended for a length of 6–7 m. After correction of the strangulation, the small intestines were decompressed by gently pushing its contents into the cecum before resection was started. Fig. 1 Intra-operative view of the strangulation in the distal jejunum. Arrow: The distal tip of the diverticulum, a hemorrhagic fat pedicle, secured the loop of strangulation. Note the surrounding dilated small intestines Fig. 2 Intra-operative view of the Meckel’s diverticulum ( a ) and jejunum ( b ) after reduction of the strangulation. The mesenteric (*) positioned diverticulum (between the black arrows) first runs parallel to the jejunum and diverges after 17 cm into a free diverticulum
4.058594
0.882813
sec[1]/sec[2]/p[1]
en
0.999996
33121487
https://doi.org/10.1186/s12917-020-02631-w
[ "strangulation", "jejunum", "diverticulum", "small", "mesenteric", "horse", "dilated", "reduction", "side", "meckel" ]
[ { "code": "PB02", "title": "Unintentional threat to breathing by strangulation" }, { "code": "GA18.5", "title": "Torsion of ovary, ovarian pedicle or fallopian tube" }, { "code": "DA91.1", "title": "Volvulus of small intestine" }, { "code": "DB1Y", "title": "Other specified diseases of appendix" }, { "code": "GC01.0", "title": "Bladder neck obstruction" }, { "code": "DE11", "title": "Dumping syndrome" }, { "code": "1A40.0&XA8UM1", "title": "Jejunitis" }, { "code": "DA94.0Z", "title": "Primary ulcer of small intestine, unspecified" }, { "code": "QF01.Y", "title": "Other specified acquired absence of organs" }, { "code": "LB15.1", "title": "Atresia of small intestine" } ]
=== ICD-11 CODES FOUND === [PB02] Unintentional threat to breathing by strangulation Also known as: Unintentional threat to breathing by strangulation | strangulation NOS | ligature strangulation NOS | Accidental suffocation and strangulation in bed | accidental mechanical suffocation in bed [GA18.5] Torsion of ovary, ovarian pedicle or fallopian tube Definition: A condition of the ovary, ovarian pedicle, and fallopian tube, caused by a benign ovarian cyst or ovarian hyperstimulation. This condition is characterised by the partial or complete rotation of the ovarian vascular pedicle and abdominal pain. Confirmation is by imaging. Also known as: Torsion of ovary, ovarian pedicle or fallopian tube | torsion of ovary and ovarian pedicle with torsion of fallopian tube | Torsion of ovary | ovarian torsion | strangulation of ovary [DA91.1] Volvulus of small intestine Definition: A volvulus is an abnormal twisting of the intestine around the axis of its own mesentery, resulting in obstruction of the more proximal bowel. Twisting of the mesentery may involve the mesenteric vessels and so make the involved loop particularly susceptible to strangulation and gangrene, with resulting perforation, peritonitis, and sepsis. Also known as: Volvulus of small intestine | small bowel loop | small bowel strangulation | SBO - [small bowel obstruction] strangulated [DB1Y] Other specified diseases of appendix Also known as: Other specified diseases of appendix | Appendiceal colic | appendicular colic | appendix colic | Adhesion of appendix [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 [DE11] Dumping syndrome Definition: Dumping syndrome is a group of signs and symptoms that develops most often in people who have had surgery to remove all or part of their stomach, or in whom surgically bypassed. It may occur early (during a meal or within 15-30 minutes after a meal with nausea, vomiting, abdominal pain, cramps, diarrhoea, dizziness, and heart palpitations) or late (1 to 3 hours after eating with sweating, weakness, fatigue, dizziness, lightheadedness, heart palpitations, and fainting). Also known as: Dumping syndrome | jejunal syndrome | postgastric surgery syndrome | postgastrectomy syndrome | post cibal syndrome [DA94.0Z] Primary ulcer of small intestine, unspecified Also known as: Primary ulcer of small intestine, unspecified | Primary ulcer of small intestine | acute jejunal ulcer | jejunal peptic ulcer | acute peptic jejunal ulcer [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 [LB15.1] Atresia of small intestine Definition: Jejunoileal atresias and stenoses are major causes of neonatal intestinal obstruction. Atresia refers to a congenital obstruction with complete occlusion of the intestinal lumen. It accounts for 95% of obstructions. Four types of jejunoileal atresias are described. They can range from having a small area of blockage or web to missing large sections of the intestines. Intestinal atresia is one of the most frequent causes of bowel obstruction in the newborn. The ileal atresia is more common than j Also known as: Atresia of small intestine | Congenital stenosis of small intestine | Congenital absence of small intestine | congenital small intestinal stricture NOS | Multiple-level intestinal atresia Includes: Congenital absence of small intestine | Congenital stenosis of small intestine === GRAPH WALKS === --- Walk 1 --- [PB02] Unintentional threat to breathing by strangulation --PARENT--> [?] Unintentional threat to breathing --CHILD--> [PB01] Unintentional threat to breathing by hanging --- Walk 2 --- [PB02] Unintentional threat to breathing by strangulation --PARENT--> [?] Unintentional threat to breathing --CHILD--> [PB01] Unintentional threat to breathing by hanging --- Walk 3 --- [GA18.5] Torsion of ovary, ovarian pedicle or fallopian tube Def: A condition of the ovary, ovarian pedicle, and fallopian tube, caused by a benign ovarian cyst or ovarian hyperstimulation. This condition is characterised by the partial or complete rotation of the o... --PARENT--> [GA18] Acquired abnormalities of ovary Def: Any condition of the ovary, caused by determinants arising after birth. These conditions are characterised by a malfunction, malformation, or another anomaly of the ovary.... --RELATED_TO--> [?] Cystic teratoma Def: A condition of the ovary, caused by abnormal proliferation due to genetic mutations, abnormal growth or division of germ cells. This condition is characterised by a benign ovarian neoplasm, and abdomi... --- Walk 4 --- [GA18.5] Torsion of ovary, ovarian pedicle or fallopian tube Def: A condition of the ovary, ovarian pedicle, and fallopian tube, caused by a benign ovarian cyst or ovarian hyperstimulation. This condition is characterised by the partial or complete rotation of the o... --PARENT--> [GA18] Acquired abnormalities of ovary Def: Any condition of the ovary, caused by determinants arising after birth. These conditions are characterised by a malfunction, malformation, or another anomaly of the ovary.... --RELATED_TO--> [?] Cystic teratoma Def: A condition of the ovary, caused by abnormal proliferation due to genetic mutations, abnormal growth or division of germ cells. This condition is characterised by a benign ovarian neoplasm, and abdomi... --- Walk 5 --- [DA91.1] Volvulus of small intestine Def: A volvulus is an abnormal twisting of the intestine around the axis of its own mesentery, resulting in obstruction of the more proximal bowel. Twisting of the mesentery may involve the mesenteric vess... --PARENT--> [DA91] Obstruction of small intestine Def: Hindrance of the passage of luminal contents in the small intestine. Obstruction of the small intestine can be partial or complete, and caused by intrinsic or extrinsic factors. Simple obstruction is ... --CHILD--> [DA91.1] Volvulus of small intestine Def: A volvulus is an abnormal twisting of the intestine around the axis of its own mesentery, resulting in obstruction of the more proximal bowel. Twisting of the mesentery may involve the mesenteric vess... --- Walk 6 --- [DA91.1] Volvulus of small intestine Def: A volvulus is an abnormal twisting of the intestine around the axis of its own mesentery, resulting in obstruction of the more proximal bowel. Twisting of the mesentery may involve the mesenteric vess... --PARENT--> [DA91] Obstruction of small intestine Def: Hindrance of the passage of luminal contents in the small intestine. Obstruction of the small intestine can be partial or complete, and caused by intrinsic or extrinsic factors. Simple obstruction is ... --EXCLUDES--> [?] Intra-abdominal hernia Def: A hernia occurs intra-abdominally through the opening covered by peritoneum....
[ "[PB02] Unintentional threat to breathing by strangulation\n --PARENT--> [?] Unintentional threat to breathing\n --CHILD--> [PB01] Unintentional threat to breathing by hanging", "[PB02] Unintentional threat to breathing by strangulation\n --PARENT--> [?] Unintentional threat to breathing\n --CHILD--> [PB01] Unintentional threat to breathing by hanging", "[GA18.5] Torsion of ovary, ovarian pedicle or fallopian tube\n Def: A condition of the ovary, ovarian pedicle, and fallopian tube, caused by a benign ovarian cyst or ovarian hyperstimulation. This condition is characterised by the partial or complete rotation of the o...\n --PARENT--> [GA18] Acquired abnormalities of ovary\n Def: Any condition of the ovary, caused by determinants arising after birth. These conditions are characterised by a malfunction, malformation, or another anomaly of the ovary....\n --RELATED_TO--> [?] Cystic teratoma\n Def: A condition of the ovary, caused by abnormal proliferation due to genetic mutations, abnormal growth or division of germ cells. This condition is characterised by a benign ovarian neoplasm, and abdomi...", "[GA18.5] Torsion of ovary, ovarian pedicle or fallopian tube\n Def: A condition of the ovary, ovarian pedicle, and fallopian tube, caused by a benign ovarian cyst or ovarian hyperstimulation. This condition is characterised by the partial or complete rotation of the o...\n --PARENT--> [GA18] Acquired abnormalities of ovary\n Def: Any condition of the ovary, caused by determinants arising after birth. These conditions are characterised by a malfunction, malformation, or another anomaly of the ovary....\n --RELATED_TO--> [?] Cystic teratoma\n Def: A condition of the ovary, caused by abnormal proliferation due to genetic mutations, abnormal growth or division of germ cells. This condition is characterised by a benign ovarian neoplasm, and abdomi...", "[DA91.1] Volvulus of small intestine\n Def: A volvulus is an abnormal twisting of the intestine around the axis of its own mesentery, resulting in obstruction of the more proximal bowel. Twisting of the mesentery may involve the mesenteric vess...\n --PARENT--> [DA91] Obstruction of small intestine\n Def: Hindrance of the passage of luminal contents in the small intestine. Obstruction of the small intestine can be partial or complete, and caused by intrinsic or extrinsic factors. Simple obstruction is ...\n --CHILD--> [DA91.1] Volvulus of small intestine\n Def: A volvulus is an abnormal twisting of the intestine around the axis of its own mesentery, resulting in obstruction of the more proximal bowel. Twisting of the mesentery may involve the mesenteric vess...", "[DA91.1] Volvulus of small intestine\n Def: A volvulus is an abnormal twisting of the intestine around the axis of its own mesentery, resulting in obstruction of the more proximal bowel. Twisting of the mesentery may involve the mesenteric vess...\n --PARENT--> [DA91] Obstruction of small intestine\n Def: Hindrance of the passage of luminal contents in the small intestine. Obstruction of the small intestine can be partial or complete, and caused by intrinsic or extrinsic factors. Simple obstruction is ...\n --EXCLUDES--> [?] Intra-abdominal hernia\n Def: A hernia occurs intra-abdominally through the opening covered by peritoneum...." ]
PB02
Unintentional threat to breathing by strangulation
[ { "from_icd11": "PB02", "icd10_code": "W76", "icd10_title": "" }, { "from_icd11": "GA18.5", "icd10_code": "N8351", "icd10_title": "Torsion of ovary and ovarian pedicle" }, { "from_icd11": "GA18.5", "icd10_code": "N83511", "icd10_title": "Torsion of right ovary and ovarian pedicle" }, { "from_icd11": "GA18.5", "icd10_code": "N8353", "icd10_title": "Torsion of ovary, ovarian pedicle and fallopian tube" }, { "from_icd11": "GA18.5", "icd10_code": "N83512", "icd10_title": "Torsion of left ovary and ovarian pedicle" }, { "from_icd11": "GA18.5", "icd10_code": "N83521", "icd10_title": "Torsion of right fallopian tube" }, { "from_icd11": "GA18.5", "icd10_code": "N8352", "icd10_title": "Torsion of fallopian tube" }, { "from_icd11": "GA18.5", "icd10_code": "N83519", "icd10_title": "Torsion of ovary and ovarian pedicle, unspecified side" }, { "from_icd11": "GA18.5", "icd10_code": "N83", "icd10_title": "Noninflammatory disorders of ovary, fallopian tube and broad ligament" }, { "from_icd11": "GA18.5", "icd10_code": "N835", "icd10_title": "Torsion of ovary, ovarian pedicle and fallopian tube" }, { "from_icd11": "DA91.1", "icd10_code": "K562", "icd10_title": "Volvulus" }, { "from_icd11": "GC01.0", "icd10_code": "N320", "icd10_title": "Bladder-neck obstruction" }, { "from_icd11": "DE11", "icd10_code": "K911", "icd10_title": "Postgastric surgery syndromes" }, { "from_icd11": "DA94.0Z", "icd10_code": "K633", "icd10_title": "Ulcer of intestine" }, { "from_icd11": "QF01.Y", "icd10_code": "Z9049", "icd10_title": "Acquired absence of other specified parts of digestive tract" } ]
W76
A 56-year-old female underwent surgery for ameloblastoma in the left mandible 2 years previously. Specialist examination revealed that the patient had swelling on the left face and neoplasm in the area surrounding the left mandibular angle and ramus, approximately 5.0 × 4.0 cm measuring in size. The patient also had a mild limitation in mouth opening, and 36, 37, and 38 were not detected in the oral cavity. According to the patient’s previous medical records and consultation report from the pathology department of our hospital, the pathological diagnosis of the patient was confirmed as ameloblastoma . The patient was diagnosed with ameloblastoma upon admission and scheduled to undergo partial mandibular resection and fibular osteocutaneous flap repair. She underwent CTA examination of the maxillofacial and the left calf prior to surgery. The obtained CTA data were imported into a software workstation for 3D reconstruction and subsequently downloaded onto a holographic display . During the operation, the left calf was automatically positioned according to the holographic display, and the perforator vessels were dissected in real-time . Fibular osteocutaneous flaps were prepared to repair the mandible, and direct sutures were placed at the donor site . After the operation, the flap fully survived, and during the 6-month follow-up, the patient expressed satisfaction with the reconstructive outcome.
3.855469
0.98291
sec[2]/sec[1]/p[0]
en
0.999998
PMC11294116
https://doi.org/10.3389/fonc.2024.1437598
[ "ameloblastoma", "mandible", "mandibular", "according", "fibular", "osteocutaneous", "flap", "repair", "calf", "holographic" ]
[ { "code": "2E83.1", "title": "Benign osteogenic tumours of bone or articular cartilage of lower jaw" }, { "code": "2B5J", "title": "Malignant miscellaneous tumours of bone or articular cartilage of other or unspecified sites" }, { "code": "2E83.0", "title": "Benign osteogenic tumours of bone or articular cartilage of skull or face" }, { "code": "2E83.Z", "title": "Benign osteogenic tumour of unspecified site" }, { "code": "DA06.Z", "title": "Diseases of jaws, unspecified" }, { "code": "DA0E.0Y&XA51B7", "title": "Mandibular hypoplasia" }, { "code": "NA03.3", "title": "Strain or sprain of jaw" }, { "code": "DA0E.7", "title": "Dentofacial parafunctional disorders" }, { "code": "NA02.7Z", "title": "Fracture of mandible, unspecified" }, { "code": "DA0E.8", "title": "Temporomandibular joint disorders" } ]
=== ICD-11 CODES FOUND === [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 [2B5J] Malignant miscellaneous tumours of bone or articular cartilage of other or unspecified sites Also known as: Malignant miscellaneous tumours of bone or articular cartilage of other or unspecified sites | Malignant miscellaneous bone tumours of bone or articular cartilage of skull or face | Malignant miscellaneous bone tumours of craniofacial bone or articular cartilage | malignant neoplasm of craniofacial bone and articular cartilage | Malignant miscellaneous bone tumours of maxillofacial bone or articular cartilage Excludes: Neoplasms of haematopoietic or lymphoid tissues [2E83.0] Benign osteogenic tumours of bone or articular cartilage of skull or face Also known as: Benign osteogenic tumours of bone or articular cartilage of skull or face | Benign neoplasm of craniofacial bones | Benign neoplasm of craniofacial bone and articular cartilage | Benign neoplasm of maxillofacial bones | benign neoplasm of maxillofacial bone and articular cartilage [2E83.Z] Benign osteogenic tumour of unspecified site Also known as: Benign osteogenic tumour of unspecified site | Benign osteogenic tumours | benign bone neoplasm | benign bone tumour | benign cartilaginous neoplasm [DA06.Z] Diseases of jaws, unspecified Also known as: Diseases of jaws, unspecified | Diseases of jaws | disease of jaw | diseases of the jaws | disorder of jaw [NA03.3] Strain or sprain of jaw Definition: A collective term for muscle and ligament injuries of the tissues associated with the mandible without dislocation or fracture; a joint injury in which some of the fibers of a supporting ligament are ruptured but the continuity of the ligament remains intact. A strain is an overstretching or overexertion of some part of the musculature. Also known as: Strain or sprain of jaw | strain of jaw | sprain of mandible | strain of mandible | sprain of temporomandibular joint [DA0E.7] Dentofacial parafunctional disorders Definition: Bruxism is a repetitive jaw-muscle activity characterised by clenching or grinding of the teeth and/or by bracing or thrusting of the mandible. Bruxism has two distinct circadian manifestations: it can occur during sleep (indicated as sleep bruxism) or during wakefulness (indicated as awake bruxism) Also known as: Dentofacial parafunctional disorders | Bruxism | Teeth-clenching | Teeth-grinding | Awake bruxism Excludes: Atypical facial pain | dyskinesia | trismus [NA02.7Z] Fracture of mandible, unspecified Also known as: Fracture of mandible, unspecified | Fracture of mandible | fracture of lower jaw | mandibular fracture | jaw fracture [DA0E.8] Temporomandibular joint disorders Definition: This is an umbrella term covering acute or chronic pain, especially in the muscles of mastication and/or inflammation of the temporomandibular joint, which connects the mandible to the skull. Also known as: Temporomandibular joint disorders | temporomandibular joint disease | temporomandibular jaw disorder | TMJ - [temporomandibular joint] disorder | temporomandibular developmental disorder of jaw Includes: Temporomandibular joint-pain-dysfunction syndrome | Derangement of temporomandibular joint | Chronic temporomandibular disorder pain Excludes: current temporomandibular joint: strain | current temporomandibular joint: dislocation === GRAPH WALKS === --- Walk 1 --- [2E83.1] Benign osteogenic tumours of bone or articular cartilage of lower jaw --PARENT--> [2E83] Benign osteogenic tumours Def: A neoplasm arising from the bone or articular cartilage that does not invade adjacent tissues or metastasize to other anatomic sites. Representative examples include benign fibrous histiocytoma of bon... --PARENT--> [?] Benign mesenchymal neoplasms Def: Bening neoplasms of muscle, fat, fibrous tissue, bone, cartilage, and blood vessels.... --- Walk 2 --- [2E83.1] Benign osteogenic tumours of bone or articular cartilage of lower jaw --PARENT--> [2E83] Benign osteogenic tumours Def: A neoplasm arising from the bone or articular cartilage that does not invade adjacent tissues or metastasize to other anatomic sites. Representative examples include benign fibrous histiocytoma of bon... --PARENT--> [?] Benign mesenchymal neoplasms Def: Bening neoplasms of muscle, fat, fibrous tissue, bone, cartilage, and blood vessels.... --- Walk 3 --- [2B5J] Malignant miscellaneous tumours of bone or articular cartilage of other or unspecified sites --EXCLUDES--> [?] Neoplasms of haematopoietic or lymphoid tissues Def: A neoplasm arising from hematopoietic or lymphoid cells found in the bone marrow, peripheral blood, lymph nodes and spleen (organs of the hematopoietic or lymphoid system). Hematopoietic or lymphoid c... --EXCLUDES--> [?] Malignant neoplasm metastasis in lymph nodes --- Walk 4 --- [2B5J] Malignant miscellaneous tumours of bone or articular cartilage of other or unspecified sites --EXCLUDES--> [?] Neoplasms of haematopoietic or lymphoid tissues Def: A neoplasm arising from hematopoietic or lymphoid cells found in the bone marrow, peripheral blood, lymph nodes and spleen (organs of the hematopoietic or lymphoid system). Hematopoietic or lymphoid c... --EXCLUDES--> [?] Malignant neoplasm metastasis in bone or bone marrow Def: The spread of a malignant neoplasm from a primary site to the skeletal system. The majority of metastatic neoplasms to the bone are carcinomas.... --- Walk 5 --- [2E83.0] Benign osteogenic tumours of bone or articular cartilage of skull or face --PARENT--> [2E83] Benign osteogenic tumours Def: A neoplasm arising from the bone or articular cartilage that does not invade adjacent tissues or metastasize to other anatomic sites. Representative examples include benign fibrous histiocytoma of bon... --CHILD--> [2E83.1] Benign osteogenic tumours of bone or articular cartilage of lower jaw --- Walk 6 --- [2E83.0] Benign osteogenic tumours of bone or articular cartilage of skull or face --PARENT--> [2E83] Benign osteogenic tumours Def: A neoplasm arising from the bone or articular cartilage that does not invade adjacent tissues or metastasize to other anatomic sites. Representative examples include benign fibrous histiocytoma of bon... --CHILD--> [2E83.2] Benign osteogenic tumours of bone or articular cartilage of vertebral column
[ "[2E83.1] Benign osteogenic tumours of bone or articular cartilage of lower jaw\n --PARENT--> [2E83] Benign osteogenic tumours\n Def: A neoplasm arising from the bone or articular cartilage that does not invade adjacent tissues or metastasize to other anatomic sites. Representative examples include benign fibrous histiocytoma of bon...\n --PARENT--> [?] Benign mesenchymal neoplasms\n Def: Bening neoplasms of muscle, fat, fibrous tissue, bone, cartilage, and blood vessels....", "[2E83.1] Benign osteogenic tumours of bone or articular cartilage of lower jaw\n --PARENT--> [2E83] Benign osteogenic tumours\n Def: A neoplasm arising from the bone or articular cartilage that does not invade adjacent tissues or metastasize to other anatomic sites. Representative examples include benign fibrous histiocytoma of bon...\n --PARENT--> [?] Benign mesenchymal neoplasms\n Def: Bening neoplasms of muscle, fat, fibrous tissue, bone, cartilage, and blood vessels....", "[2B5J] Malignant miscellaneous tumours of bone or articular cartilage of other or unspecified sites\n --EXCLUDES--> [?] Neoplasms of haematopoietic or lymphoid tissues\n Def: A neoplasm arising from hematopoietic or lymphoid cells found in the bone marrow, peripheral blood, lymph nodes and spleen (organs of the hematopoietic or lymphoid system). Hematopoietic or lymphoid c...\n --EXCLUDES--> [?] Malignant neoplasm metastasis in lymph nodes", "[2B5J] Malignant miscellaneous tumours of bone or articular cartilage of other or unspecified sites\n --EXCLUDES--> [?] Neoplasms of haematopoietic or lymphoid tissues\n Def: A neoplasm arising from hematopoietic or lymphoid cells found in the bone marrow, peripheral blood, lymph nodes and spleen (organs of the hematopoietic or lymphoid system). Hematopoietic or lymphoid c...\n --EXCLUDES--> [?] Malignant neoplasm metastasis in bone or bone marrow\n Def: The spread of a malignant neoplasm from a primary site to the skeletal system. The majority of metastatic neoplasms to the bone are carcinomas....", "[2E83.0] Benign osteogenic tumours of bone or articular cartilage of skull or face\n --PARENT--> [2E83] Benign osteogenic tumours\n Def: A neoplasm arising from the bone or articular cartilage that does not invade adjacent tissues or metastasize to other anatomic sites. Representative examples include benign fibrous histiocytoma of bon...\n --CHILD--> [2E83.1] Benign osteogenic tumours of bone or articular cartilage of lower jaw", "[2E83.0] Benign osteogenic tumours of bone or articular cartilage of skull or face\n --PARENT--> [2E83] Benign osteogenic tumours\n Def: A neoplasm arising from the bone or articular cartilage that does not invade adjacent tissues or metastasize to other anatomic sites. Representative examples include benign fibrous histiocytoma of bon...\n --CHILD--> [2E83.2] Benign osteogenic tumours of bone or articular cartilage of vertebral column" ]
2E83.1
Benign osteogenic tumours of bone or articular cartilage of lower jaw
[ { "from_icd11": "2E83.1", "icd10_code": "D165", "icd10_title": "Benign neoplasm of lower jaw bone" }, { "from_icd11": "2B5J", "icd10_code": "C419", "icd10_title": "Malignant neoplasm of bone and articular cartilage, unspecified" }, { "from_icd11": "2B5J", "icd10_code": "C418", "icd10_title": "" }, { "from_icd11": "2E83.0", "icd10_code": "D164", "icd10_title": "Benign neoplasm of bones of skull and face" }, { "from_icd11": "2E83.Z", "icd10_code": "Q784", "icd10_title": "Enchondromatosis" }, { "from_icd11": "2E83.Z", "icd10_code": "D169", "icd10_title": "Benign neoplasm of bone and articular cartilage, unspecified" }, { "from_icd11": "2E83.Z", "icd10_code": "D16", "icd10_title": "Benign neoplasm of bone and articular cartilage" }, { "from_icd11": "NA03.3", "icd10_code": "S034", "icd10_title": "Sprain of jaw" }, { "from_icd11": "NA02.7Z", "icd10_code": "S02652A", "icd10_title": "Fracture of angle of left mandible, initial encounter for closed fracture" }, { "from_icd11": "NA02.7Z", "icd10_code": "S0262XA", "icd10_title": "" }, { "from_icd11": "NA02.7Z", "icd10_code": "S02610A", "icd10_title": "Fracture of condylar process of mandible, unspecified side, initial encounter for closed fracture" }, { "from_icd11": "NA02.7Z", "icd10_code": "S02641A", "icd10_title": "Fracture of ramus of right mandible, initial encounter for closed fracture" }, { "from_icd11": "NA02.7Z", "icd10_code": "S0269XA", "icd10_title": "Fracture of mandible of other specified site, initial encounter for closed fracture" }, { "from_icd11": "NA02.7Z", "icd10_code": "S0261XA", "icd10_title": "" }, { "from_icd11": "NA02.7Z", "icd10_code": "S0266XB", "icd10_title": "Fracture of symphysis of mandible, initial encounter for open fracture" } ]
D165
Benign neoplasm of lower jaw bone
A 56-year-old African American female patient presented to the hospital with two weeks of progressively worsening generalized fatigue, lightheadedness, and dyspnea on exertion. The patient had a history of depression and was recently prescribed duloxetine. The patient endorsed some weight loss over the past three months due to decreased PO intake from depression, however, denied any other past medical history. The patient did not follow a vegetarian/vegan diet. She denied any neurological symptoms, including paresthesias, weakness, or sensory changes. She denied any obvious bleeding, extremity pain or swelling, surgery, recent travel, or immobility. The patient was not taking any medications despite being prescribed duloxetine-she had self-discontinued after a week. The patient had a history of five biological children with one miscarriage. She also denied any chest pain, palpitations, orthopnea, or family history of cardiac disease. She endorsed no history of smoking or alcohol use. Moreover, the patient also did not have any history of cancer or lower extremity infection. The physical exam was unremarkable including a full neurological exam with no lower extremity swelling or pain. The patient's BMI was elevated to 34.1 kg/m 2 consistent with obesity. The patient was noted to be afebrile and normotensive, but tachycardic on vital signs with EKG showing sinus tachycardia without any ST changes.
3.648438
0.985352
sec[1]/p[0]
en
0.999997
40357099
https://doi.org/10.7759/cureus.82151
[ "denied", "extremity", "pain", "depression", "prescribed", "duloxetine", "endorsed", "past", "neurological", "including" ]
[ { "code": "LD2A.Y", "title": "Other specified malformative disorders of sex development" }, { "code": "ND56.1", "title": "Open wound of unspecified body region" }, { "code": "LB9Z", "title": "Structural developmental anomalies of the skeleton, unspecified" }, { "code": "FB56.6", "title": "Other specified soft tissue disorders" }, { "code": "5B51&XS25", "title": "Severe wasting in infants, children or adolescents" }, { "code": "ND55", "title": "Other injuries of leg, level unspecified" }, { "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" } ]
=== ICD-11 CODES FOUND === [LD2A.Y] Other specified malformative disorders of sex development Also known as: Other specified malformative disorders of sex development | 45, X, 46, XY gonadal dysgenesis | Mixed gonadal dysgenesis | Streak testis | 46, XX disorders of sex development [ND56.1] Open wound of unspecified body region Also known as: Open wound of unspecified body region | cut NOS | open wound NOS | penetrating wound NOS | Puncture wound with foreign body unspecified body region Excludes: Traumatic amputations involving multiple body regions | Open wounds involving multiple body regions | traumatic amputation NOS [LB9Z] Structural developmental anomalies of the skeleton, unspecified Also known as: Structural developmental anomalies of the skeleton, unspecified | Abnormal bone development | skeletal anomaly NOS [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 [ND55] Other injuries of leg, level unspecified Also known as: Other injuries of leg, level unspecified | other injuries of lower limb, level unspecified | Superficial injury of leg, level unspecified | Abrasion of leg, level unspecified | Contusion of leg, level unspecified Excludes: Fracture of leg, level unspecified | Injuries involving multiple body regions [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 === GRAPH WALKS === --- Walk 1 --- [LD2A.Y] Other specified malformative disorders of sex development --PARENT--> [LD2A] Malformative disorders of sex development Def: Any condition caused by failure of the genitals to correctly develop during the antenatal period.... --RELATED_TO--> [?] 46,XX disorders of sex development induced by androgens of maternal origin Def: This refers to 46,XX disorders of sex development induced by any natural or synthetic compound, usually a steroid hormone, that stimulates or controls the development and maintenance of male character... --- Walk 2 --- [LD2A.Y] Other specified malformative disorders of sex development --PARENT--> [LD2A] Malformative disorders of sex development Def: Any condition caused by failure of the genitals to correctly develop during the antenatal period.... --CHILD--> [LD2A.2] Testicular agenesis Def: A rare 46,XY disorder of gonadal development characterized by congenital complete absence of testicular tissue in an individual with an otherwise male phenotype and normal karyotype. In addition, a sm... --- Walk 3 --- [ND56.1] Open wound of unspecified body region --EXCLUDES--> [?] Traumatic amputations involving multiple body regions --CHILD--> [?] Traumatic amputation of both hands --- Walk 4 --- [ND56.1] Open wound of unspecified body region --EXCLUDES--> [?] Open wounds involving multiple body regions --CHILD--> [?] Open wounds involving multiple regions of arm --- Walk 5 --- [LB9Z] Structural developmental anomalies of the skeleton, unspecified --PARENT--> [?] Structural developmental anomalies of the skeleton Def: A deformation established before birth of an anatomical structure of one or more bones.... --CHILD--> [LB70] Structural developmental anomalies of cranium Def: Any condition caused by failure of the cranium to correctly develop during the antenatal period.... --- Walk 6 --- [LB9Z] Structural developmental anomalies of the skeleton, unspecified --PARENT--> [?] Structural developmental anomalies of the skeleton Def: A deformation established before birth of an anatomical structure of one or more bones.... --CHILD--> [LB72] Structural developmental anomalies of shoulder girdle Def: Any condition caused by failure of the shoulder girdle to correctly develop during the antenatal period....
[ "[LD2A.Y] Other specified malformative disorders of sex development\n --PARENT--> [LD2A] Malformative disorders of sex development\n Def: Any condition caused by failure of the genitals to correctly develop during the antenatal period....\n --RELATED_TO--> [?] 46,XX disorders of sex development induced by androgens of maternal origin\n Def: This refers to 46,XX disorders of sex development induced by any natural or synthetic compound, usually a steroid hormone, that stimulates or controls the development and maintenance of male character...", "[LD2A.Y] Other specified malformative disorders of sex development\n --PARENT--> [LD2A] Malformative disorders of sex development\n Def: Any condition caused by failure of the genitals to correctly develop during the antenatal period....\n --CHILD--> [LD2A.2] Testicular agenesis\n Def: A rare 46,XY disorder of gonadal development characterized by congenital complete absence of testicular tissue in an individual with an otherwise male phenotype and normal karyotype. In addition, a sm...", "[ND56.1] Open wound of unspecified body region\n --EXCLUDES--> [?] Traumatic amputations involving multiple body regions\n --CHILD--> [?] Traumatic amputation of both hands", "[ND56.1] Open wound of unspecified body region\n --EXCLUDES--> [?] Open wounds involving multiple body regions\n --CHILD--> [?] Open wounds involving multiple regions of arm", "[LB9Z] Structural developmental anomalies of the skeleton, unspecified\n --PARENT--> [?] Structural developmental anomalies of the skeleton\n Def: A deformation established before birth of an anatomical structure of one or more bones....\n --CHILD--> [LB70] Structural developmental anomalies of cranium\n Def: Any condition caused by failure of the cranium to correctly develop during the antenatal period....", "[LB9Z] Structural developmental anomalies of the skeleton, unspecified\n --PARENT--> [?] Structural developmental anomalies of the skeleton\n Def: A deformation established before birth of an anatomical structure of one or more bones....\n --CHILD--> [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...." ]
LD2A.Y
Other specified malformative disorders of sex development
[ { "from_icd11": "ND56.1", "icd10_code": "T141", "icd10_title": "" }, { "from_icd11": "LB9Z", "icd10_code": "Q8789", "icd10_title": "Other specified congenital malformation syndromes, not elsewhere classified" }, { "from_icd11": "LB9Z", "icd10_code": "Q8781", "icd10_title": "Alport syndrome" }, { "from_icd11": "LB9Z", "icd10_code": "Q742", "icd10_title": "Other congenital malformations of lower limb(s), including pelvic girdle" }, { "from_icd11": "LB9Z", "icd10_code": "Q749", "icd10_title": "Unspecified congenital malformation of limb(s)" }, { "from_icd11": "LB9Z", "icd10_code": "Q740", "icd10_title": "Other congenital malformations of upper limb(s), including shoulder girdle" }, { "from_icd11": "LB9Z", "icd10_code": "Q741", "icd10_title": "Congenital malformation of knee" }, { "from_icd11": "LB9Z", "icd10_code": "Q875", "icd10_title": "Other congenital malformation syndromes with other skeletal changes" }, { "from_icd11": "LB9Z", "icd10_code": "Q748", "icd10_title": "Other specified congenital malformations of limb(s)" }, { "from_icd11": "LB9Z", "icd10_code": "Q89", "icd10_title": "Other congenital malformations, not elsewhere classified" }, { "from_icd11": "LB9Z", "icd10_code": "Q65-Q79", "icd10_title": "" }, { "from_icd11": "LB9Z", "icd10_code": "Q73", "icd10_title": "Reduction defects of unspecified limb" }, { "from_icd11": "LB9Z", "icd10_code": "Q730", "icd10_title": "Congenital absence of unspecified limb(s)" }, { "from_icd11": "LB9Z", "icd10_code": "Q731", "icd10_title": "Phocomelia, unspecified limb(s)" }, { "from_icd11": "LB9Z", "icd10_code": "Q74", "icd10_title": "Other congenital malformations of limb(s)" } ]
T141
A 68‐year‐old Japanese woman with a surgical history of total aortic arch replacement for a distal aortic arch aneurysm 20 years earlier visited our hospital because of back pain for three days and haemoptysis. Chest non‐contrast computed tomography (NCCT) was performed because of a contrast agent allergy and showed an abnormal mediastinal mass‐like lesion in the subaortic region . The radiologist and pulmonologist were unable to definitively diagnose the mediastinal mass as a neoplastic or vascular abnormality, so computed tomography (CT) angiography was performed after pre‐medication, which revealed contrast medium extravasation from the vicinity of the anastomotic site of the artificial blood vessel of the aortic arch, suggestive of pseudoaneurysm in the mediastinal area . She was immediately transferred to the cardiovascular surgery department and underwent emergency stent graft insertion. A pseudoaneurysm occurring a long time after thoracic replacement is extremely rare, and only one case has been previously reported in which the patient developed a pseudoaneurysm more than 20 years after undergoing cardiac surgery . In this patient, CT angiography should have been performed according to the chest CT protocol because of her symptoms of haemoptysis and back pain. With the growing diversity in chest CT protocols, physicians need to choose the recommended protocols for individual indications.
3.986328
0.967773
sec[0]/p[0]
en
0.999997
32832089
https://doi.org/10.1002/rcr2.645
[ "aortic", "arch", "because", "chest", "contrast", "mediastinal", "pseudoaneurysm", "replacement", "back", "pain" ]
[ { "code": "BD5Z", "title": "Diseases of arteries or arterioles, unspecified" }, { "code": "LA8A.3", "title": "Congenital supravalvar aortic stenosis" }, { "code": "BD40.1", "title": "Atherosclerosis of aorta" }, { "code": "BB71.Z", "title": "Aortic valve insufficiency, unspecified" }, { "code": "LA8B.2Y", "title": "Other specified congenital anomaly of aorta or its branches" }, { "code": "FA31.5", "title": "Acquired pes planus" }, { "code": "LA8B.24", "title": "Congenital anomaly of aortic arch branch" }, { "code": "4A44.1", "title": "Aortic arch syndrome" }, { "code": "LB98.1", "title": "Congenital pes planus" }, { "code": "QC10", "title": "Procedure not carried out because of contraindication" } ]
=== ICD-11 CODES FOUND === [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 [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 [BD40.1] Atherosclerosis of aorta Also known as: Atherosclerosis of aorta | aorta atheroma | aorta calcification | aorta arteriosclerosis | aortic degeneration [BB71.Z] Aortic valve insufficiency, unspecified Also known as: Aortic valve insufficiency, unspecified | Aortic valve insufficiency | aortic insufficiency | aortic valve incompetency | AI - [aortic incompetence] [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 [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 [LA8B.24] Congenital anomaly of aortic arch branch Definition: A congenital cardiovascular malformation of one or more branches of the aortic arch (innominate, carotid, or subclavian arteries). Also known as: Congenital anomaly of aortic arch branch | Aberrant origin of right subclavian artery | aberrant right subclavian artery syndrome | ARSA - [aberrant right subclavian artery] | ARSCA - [aberrant right subclavian artery] [4A44.1] Aortic arch syndrome Definition: Arteritis, often granulomatous, predominantly affecting the aorta and/or its major branches. Onset usually in patients younger than 50. Also known as: Aortic arch syndrome | obliterative aortitis | aortic arch arteritis | subclavian-carotid obstruction syndrome | idiopathic medial aortopathy and arteriopathy [LB98.1] Congenital pes planus Definition: 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. Also known as: Congenital pes planus | congenital rocker bottom flat foot | congenital pes planovalgus | congenital weak arches | congenital fallen arches Includes: congenital flat foot [QC10] Procedure not carried out because of contraindication Also known as: Procedure not carried out because of contraindication | intervention not carried out because of contraindication | Procedure cancelled due to contraindication === GRAPH WALKS === --- Walk 1 --- [BD5Z] Diseases of arteries or arterioles, unspecified --PARENT--> [?] Diseases of arteries or arterioles --CHILD--> [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 --- [BD5Z] Diseases of arteries or arterioles, unspecified --PARENT--> [?] Diseases of arteries or arterioles --EXCLUDES--> [?] Diseases of coronary artery Def: Conditions affecting the blood perfusion of the heart.... --- Walk 3 --- [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--> [?] Congenital subaortic stenosis --- Walk 4 --- [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... --PARENT--> [?] Congenital anomaly of aortic valve Def: A congenital cardiovascular malformation where the aortic valve is abnormal.... --- Walk 5 --- [BD40.1] Atherosclerosis of aorta --PARENT--> [BD40] Atherosclerotic chronic arterial occlusive disease --EXCLUDES--> [?] Coronary atherosclerosis Def: Atherosclerosis is the build up inside the coronary arteries of cholesterol, fatty acids, calcium, fibrous connective tissue and cells (mostly macrophages), referred to as plaque. The effect of this i... --- Walk 6 --- [BD40.1] Atherosclerosis of aorta --PARENT--> [BD40] Atherosclerotic chronic arterial occlusive disease --EXCLUDES--> [?] Chronic vascular disorders of intestine
[ "[BD5Z] Diseases of arteries or arterioles, unspecified\n --PARENT--> [?] Diseases of arteries or arterioles\n --CHILD--> [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. ...", "[BD5Z] Diseases of arteries or arterioles, unspecified\n --PARENT--> [?] Diseases of arteries or arterioles\n --EXCLUDES--> [?] Diseases of coronary artery\n Def: Conditions affecting the blood perfusion of the heart....", "[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--> [?] Congenital subaortic stenosis", "[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 --PARENT--> [?] Congenital anomaly of aortic valve\n Def: A congenital cardiovascular malformation where the aortic valve is abnormal....", "[BD40.1] Atherosclerosis of aorta\n --PARENT--> [BD40] Atherosclerotic chronic arterial occlusive disease\n --EXCLUDES--> [?] Coronary atherosclerosis\n Def: Atherosclerosis is the build up inside the coronary arteries of cholesterol, fatty acids, calcium, fibrous connective tissue and cells (mostly macrophages), referred to as plaque. The effect of this i...", "[BD40.1] Atherosclerosis of aorta\n --PARENT--> [BD40] Atherosclerotic chronic arterial occlusive disease\n --EXCLUDES--> [?] Chronic vascular disorders of intestine" ]
BD5Z
Diseases of arteries or arterioles, unspecified
[ { "from_icd11": "BD5Z", "icd10_code": "I7389", "icd10_title": "Other specified peripheral vascular diseases" }, { "from_icd11": "BD5Z", "icd10_code": "I7419", "icd10_title": "Embolism and thrombosis of other parts of aorta" }, { "from_icd11": "BD5Z", "icd10_code": "I7411", "icd10_title": "Embolism and thrombosis of thoracic aorta" }, { "from_icd11": "BD5Z", "icd10_code": "I7410", "icd10_title": "Embolism and thrombosis of unspecified parts of aorta" }, { "from_icd11": "BD5Z", "icd10_code": "I7381", "icd10_title": "Erythromelalgia" }, { "from_icd11": "BD5Z", "icd10_code": "I745", "icd10_title": "Embolism and thrombosis of iliac artery" }, { "from_icd11": "BD5Z", "icd10_code": "I789", "icd10_title": "Disease of capillaries, unspecified" }, { "from_icd11": "BD5Z", "icd10_code": "I748", "icd10_title": "Embolism and thrombosis of other arteries" }, { "from_icd11": "BD5Z", "icd10_code": "I749", "icd10_title": "Embolism and thrombosis of unspecified artery" }, { "from_icd11": "BD5Z", "icd10_code": "I781", "icd10_title": "Nevus, non-neoplastic" }, { "from_icd11": "BD5Z", "icd10_code": "I788", "icd10_title": "Other diseases of capillaries" }, { "from_icd11": "BD5Z", "icd10_code": "I744", "icd10_title": "Embolism and thrombosis of arteries of extremities, unspecified" }, { "from_icd11": "BD5Z", "icd10_code": "I70-I79", "icd10_title": "" }, { "from_icd11": "BD5Z", "icd10_code": "I74", "icd10_title": "Arterial embolism and thrombosis" }, { "from_icd11": "BD5Z", "icd10_code": "I73", "icd10_title": "Other peripheral vascular diseases" } ]
I7389
Other specified peripheral vascular diseases
Given the large size of the PAA, the patient was evaluated by an adult congenital heart specialist as well as by the cardiovascular surgery service. She underwent right and left heart catheterization that demonstrated a normal peak gradient (8 mmHg) across the pulmonic valve, normal right- and left-sided pressures, and angiographically normal coronary arteries. Cardiac CT was performed for additional anatomic assessment with a PAA of 62.6 × 61.7 mm without thrombus within the aneurysm sac . The pulmonic root and RVOT were normal in size; there was no evidence of compression of adjacent structures . Surgical intervention was ultimately deferred due to her asymptomatic status and absence of high-risk features such as pulmonary hypertension, sac thrombus, compressive effect on the surrounding structures, and insufficient evidence for rate of growth of the aneurysm. Multidisciplinary cardiovascular team discussion concluded medical management with close follow-up was the best strategy. The patient is scheduled for serial imaging to monitor for growth in the size of the aneurysm and clinical surveillance for development of resultant complications. She will undergo annual transthoracic echocardiogram to monitor for development of pulmonary regurgitation and pulmonary hypertension. Strict blood pressure control was also recommended. She was instructed to avoid heavy lifting and high intensity workouts.
3.878906
0.974121
sec[4]/p[0]
en
0.999997
33110662
https://doi.org/10.1155/2020/8885260
[ "aneurysm", "pulmonary", "heart", "cardiovascular", "pulmonic", "thrombus", "evidence", "structures", "hypertension", "growth" ]
[ { "code": "BD51.Z", "title": "Aneurysm and dissection of unspecified artery" }, { "code": "BD75.Y", "title": "Venous varicosities of other specified sites" }, { "code": "BA81", "title": "Coronary artery aneurysm" }, { "code": "BB02.1Z", "title": "Aneurysm of pulmonary artery, unspecified" }, { "code": "BD51.4", "title": "Aneurysm or dissection of renal artery" }, { "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" } ]
=== ICD-11 CODES FOUND === [BD51.Z] Aneurysm and dissection of unspecified artery Also known as: Aneurysm and dissection of unspecified artery | Arterial aneurysm or dissection, excluding aorta | cirsoid aneurysm NOS | false aneurysm NOS | ruptured aneurysm NOS [BD75.Y] Venous varicosities of other specified sites Also known as: Venous varicosities of other specified sites | Caput medusae | Jugular venous aneurysm | jugular vein aneurysm | Orbital varices [BA81] Coronary artery aneurysm Definition: Coronary dilatation which exceeds the diameter of normal adjacent segments or the diameter of the patient's largest coronary vessel by 1.5 times. Also known as: Coronary artery aneurysm | aneurysm of coronary vessels | aneurysmal lesion of coronary artery | arteriovenous aneurysm of coronary vessels | coronary aneurysm Excludes: Congenital coronary arterial aneurysm | Mucocutaneous lymph node syndrome [BB02.1Z] Aneurysm of pulmonary artery, unspecified Also known as: Aneurysm of pulmonary artery, unspecified | Aneurysm of pulmonary artery | pulmonary artery aneurysm | PA - [pulmonary artery aneurysm] | pulmonary aneurysm [BD51.4] Aneurysm or dissection of renal artery Also known as: Aneurysm or dissection of renal artery | aneurysm of renal artery | renal artery aneurysm | renal aneurysm [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 === GRAPH WALKS === --- Walk 1 --- [BD51.Z] Aneurysm and dissection of unspecified artery --PARENT--> [BD51] Arterial aneurysm or dissection, excluding aorta --EXCLUDES--> [?] Acute myocardial infarction, without specification of ST elevation Def: This is commonly known as a heart attack, results from the interruption of blood supply to a part of the heart, causing heart cells to die. This is most commonly due to occlusion (blockage) of a coron... --- Walk 2 --- [BD51.Z] Aneurysm and dissection of unspecified artery --PARENT--> [BD51] Arterial aneurysm or dissection, excluding aorta --CHILD--> [BD51.2] Aneurysm or dissection of other precerebral arteries --- Walk 3 --- [BD75.Y] Venous varicosities of other specified sites --PARENT--> [BD75] Venous varicosities of sites other than lower extremity --CHILD--> [BD75.0] Sublingual varices Def: Varicose veins on the underside of the tongue... --- Walk 4 --- [BD75.Y] Venous varicosities of other specified sites --PARENT--> [BD75] Venous varicosities of sites other than lower extremity --CHILD--> [BD75.1] Scrotal varices --- Walk 5 --- [BA81] Coronary artery aneurysm Def: Coronary dilatation which exceeds the diameter of normal adjacent segments or the diameter of the patient's largest coronary vessel by 1.5 times.... --EXCLUDES--> [?] Congenital coronary arterial aneurysm Def: A congenital cardiovascular malformation in which there is one or more localized dilation(s) of a coronary vessel. Additional information: coronary artery aneurysms are usually seen in two forms, sa... --PARENT--> [?] Congenital anomaly of coronary artery Def: A congenital cardiovascular malformation of a coronary artery. This includes absence of a coronary, anomalous origin or course, dilation or stenosis, and fistulas. Additional information: congenital ... --- Walk 6 --- [BA81] Coronary artery aneurysm Def: Coronary dilatation which exceeds the diameter of normal adjacent segments or the diameter of the patient's largest coronary vessel by 1.5 times.... --EXCLUDES--> [?] Congenital coronary arterial aneurysm Def: A congenital cardiovascular malformation in which there is one or more localized dilation(s) of a coronary vessel. Additional information: coronary artery aneurysms are usually seen in two forms, sa... --PARENT--> [?] Congenital anomaly of coronary artery Def: A congenital cardiovascular malformation of a coronary artery. This includes absence of a coronary, anomalous origin or course, dilation or stenosis, and fistulas. Additional information: congenital ...
[ "[BD51.Z] Aneurysm and dissection of unspecified artery\n --PARENT--> [BD51] Arterial aneurysm or dissection, excluding aorta\n --EXCLUDES--> [?] Acute myocardial infarction, without specification of ST elevation\n Def: This is commonly known as a heart attack, results from the interruption of blood supply to a part of the heart, causing heart cells to die. This is most commonly due to occlusion (blockage) of a coron...", "[BD51.Z] Aneurysm and dissection of unspecified artery\n --PARENT--> [BD51] Arterial aneurysm or dissection, excluding aorta\n --CHILD--> [BD51.2] Aneurysm or dissection of other precerebral arteries", "[BD75.Y] Venous varicosities of other specified sites\n --PARENT--> [BD75] Venous varicosities of sites other than lower extremity\n --CHILD--> [BD75.0] Sublingual varices\n Def: Varicose veins on the underside of the tongue...", "[BD75.Y] Venous varicosities of other specified sites\n --PARENT--> [BD75] Venous varicosities of sites other than lower extremity\n --CHILD--> [BD75.1] Scrotal varices", "[BA81] Coronary artery aneurysm\n Def: Coronary dilatation which exceeds the diameter of normal adjacent segments or the diameter of the patient's largest coronary vessel by 1.5 times....\n --EXCLUDES--> [?] Congenital coronary arterial aneurysm\n Def: A congenital cardiovascular malformation in which there is one or more localized dilation(s) of a coronary vessel. \n\nAdditional information: coronary artery aneurysms are usually seen in two forms, sa...\n --PARENT--> [?] Congenital anomaly of coronary artery\n Def: A congenital cardiovascular malformation of a coronary artery. This includes absence of a coronary, anomalous origin or course, dilation or stenosis, and fistulas.\n\nAdditional information: congenital ...", "[BA81] Coronary artery aneurysm\n Def: Coronary dilatation which exceeds the diameter of normal adjacent segments or the diameter of the patient's largest coronary vessel by 1.5 times....\n --EXCLUDES--> [?] Congenital coronary arterial aneurysm\n Def: A congenital cardiovascular malformation in which there is one or more localized dilation(s) of a coronary vessel. \n\nAdditional information: coronary artery aneurysms are usually seen in two forms, sa...\n --PARENT--> [?] Congenital anomaly of coronary artery\n Def: A congenital cardiovascular malformation of a coronary artery. This includes absence of a coronary, anomalous origin or course, dilation or stenosis, and fistulas.\n\nAdditional information: congenital ..." ]
BD51.Z
Aneurysm and dissection of unspecified artery
[ { "from_icd11": "BD51.Z", "icd10_code": "I728", "icd10_title": "Aneurysm of other specified arteries" }, { "from_icd11": "BD51.Z", "icd10_code": "I729", "icd10_title": "Aneurysm of unspecified site" }, { "from_icd11": "BD51.Z", "icd10_code": "I72", "icd10_title": "Other aneurysm" }, { "from_icd11": "BA81", "icd10_code": "I2542", "icd10_title": "Coronary artery dissection" }, { "from_icd11": "BA81", "icd10_code": "I2541", "icd10_title": "Coronary artery aneurysm" }, { "from_icd11": "BA81", "icd10_code": "I254", "icd10_title": "Coronary artery aneurysm and dissection" }, { "from_icd11": "BB02.1Z", "icd10_code": "I281", "icd10_title": "Aneurysm of pulmonary artery" }, { "from_icd11": "BD51.4", "icd10_code": "I722", "icd10_title": "Aneurysm of renal artery" }, { "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" } ]
I728
Aneurysm of other specified arteries
During hospitalization, patient underwent a lumbar puncture (LP) with studies demonstrating xanthochromia, 482 nucleated cells with 29% neutrophils and 60% lymphocytes, 12 red blood cells, glucose 41 and total protein 271, most consistent with lymphocytic pleocytosis. She was started on broad-spectrum antibiotics (cefepime and vancomycin) initially. Routine electroencephalogram (EEG) was negative for seizures. Ophthalmology was consulted based on the MRI findings and patient was found to have normal visual acuity, visual fields consistent with left superior homonymous quadrantanopia, with no papilledema. Neurosurgery was also consulted and after discussion with the tumor board, plan was to obtain biopsy of the lesion. Patient underwent right supraorbital craniotomy for biopsy of the lesion. Surgical pathology showed noncaseating granulomatous inflammation most consistent with neuro-sarcoidosis. Her post-op labs were remarkable for cortisol <1.0, indicating adrenal insufficiency. No other endocrinopathies were noted pre- and post-surgery. Her serum and CNS angiotensin-converting enzyme (ACE) were negative. Other tests including cerebrospinal fluid (CSF) cytology, bacterial CSF culture, meningitis panel, HIV, and tuberculosis TB-Quantiferon test were all negative. Patient also had CT chest as part of sarcoidosis workup. CT chest showed no hilar or mediastinal adenopathy concerning for sarcoidosis.
3.902344
0.979492
sec[1]/p[3]
en
0.999996
33240714
https://doi.org/10.7759/cureus.11119
[ "consistent", "sarcoidosis", "cells", "consulted", "visual", "biopsy", "lesion", "chest", "hospitalization", "lumbar" ]
[ { "code": "MF8Y", "title": "Other specified clinical findings in specimens from the urinary system" }, { "code": "4B20.Z", "title": "Sarcoidosis, unspecified" }, { "code": "4B20.Y", "title": "Other specified sarcoidosis" }, { "code": "4B20.5", "title": "Cutaneous sarcoidosis" }, { "code": "4B20.4", "title": "Ocular sarcoidosis" }, { "code": "4B20.0", "title": "Sarcoidosis of lung" }, { "code": "MF9Y", "title": "Other specified clinical findings on examination of urine, without diagnosis" }, { "code": "5C56.20", "title": "Mucolipidosis" }, { "code": "3A51.1", "title": "Sickle cell disease without crisis" }, { "code": "9A96.3", "title": "Primary anterior uveitis" } ]
=== ICD-11 CODES FOUND === [MF8Y] Other specified clinical findings in specimens from the urinary system Also known as: Other specified clinical findings in specimens from the urinary system | Glomerular disease with minor glomerular abnormality | Glomerular disease with minimal change disease | Secondary glomerular disease with minor glomerular abnormality | Glomerular disease with minor glomerular abnormality in diseases classified elsewhere [4B20.Z] Sarcoidosis, unspecified Also known as: Sarcoidosis, unspecified | Sarcoidosis | Besnier-Boeck-Schaumann disease | Boeck's disease | Boeck's sarcoid [4B20.Y] Other specified sarcoidosis Also known as: Other specified sarcoidosis | Sarcoidosis of lung with sarcoidosis of lymph nodes | Sarcoidosis of the musculoskeletal system | Sarcoid arthropathy | arthritis secondary to sarcoidosis [4B20.5] Cutaneous sarcoidosis Also known as: Cutaneous sarcoidosis | Sarcoidosis of skin | Acute sarcoidosis with erythema nodosum | Löfgren syndrome | Papular, micropapular or lichenoid sarcoidosis [4B20.4] Ocular sarcoidosis Definition: This is a syndrome involving abnormal collections of chronic inflammatory cells (granulomas) that can form as nodules in multiple organs. Also known as: Ocular sarcoidosis | Sarcoid associated anterior uveitis | Iridocyclitis in sarcoidosis [4B20.0] Sarcoidosis of lung Also known as: Sarcoidosis of lung | lung sarcoid | pulmonary sarcoidosis | sarcoidosis in lung [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) [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] [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 === GRAPH WALKS === --- Walk 1 --- [MF8Y] Other specified clinical findings in specimens from the urinary system --PARENT--> [?] Clinical findings in specimens from the urinary system --CHILD--> [MF80] Diffuse mesangial sclerosis Def: Diffuse mesangial sclerosis is a histological appearance which is characterised by diffuse thickening of basement membrane and massive enlargement of mesangial areas leading to contraction and scleros... --- Walk 2 --- [MF8Y] Other specified clinical findings in specimens from the urinary system --PARENT--> [?] Clinical findings in specimens from the urinary system --PARENT--> [?] Symptoms, signs or clinical findings of the genitourinary system --- Walk 3 --- [4B20.Z] Sarcoidosis, unspecified --PARENT--> [4B20] Sarcoidosis Def: Sarcoidosis is a multisystem disorder of unknown cause characterised by the formation of immune granulomas in involved organs. The lung and the lymphatic system are predominantly affected, but virtual... --CHILD--> [4B20.2] Sarcoidosis of the digestive system Def: This is a syndrome involving abnormal collections of chronic inflammatory cells (granulomas) that can form as nodules in the digestive system.... --- Walk 4 --- [4B20.Z] Sarcoidosis, unspecified --PARENT--> [4B20] Sarcoidosis Def: Sarcoidosis is a multisystem disorder of unknown cause characterised by the formation of immune granulomas in involved organs. The lung and the lymphatic system are predominantly affected, but virtual... --CHILD--> [4B20.1] Sarcoidosis of lymph nodes Def: Lymphadenopathy is very common in sarcoidosis. Intrathoracic nodes are enlarged in 75 to 90% of all patients; usually this involves the hilar nodes, but the paratracheal nodes are commonly involved. P... --- Walk 5 --- [4B20.Y] Other specified sarcoidosis --PARENT--> [4B20] Sarcoidosis Def: Sarcoidosis is a multisystem disorder of unknown cause characterised by the formation of immune granulomas in involved organs. The lung and the lymphatic system are predominantly affected, but virtual... --CHILD--> [4B20.1] Sarcoidosis of lymph nodes Def: Lymphadenopathy is very common in sarcoidosis. Intrathoracic nodes are enlarged in 75 to 90% of all patients; usually this involves the hilar nodes, but the paratracheal nodes are commonly involved. P... --- Walk 6 --- [4B20.Y] Other specified sarcoidosis --PARENT--> [4B20] Sarcoidosis Def: Sarcoidosis is a multisystem disorder of unknown cause characterised by the formation of immune granulomas in involved organs. The lung and the lymphatic system are predominantly affected, but virtual... --CHILD--> [4B20.1] Sarcoidosis of lymph nodes Def: Lymphadenopathy is very common in sarcoidosis. Intrathoracic nodes are enlarged in 75 to 90% of all patients; usually this involves the hilar nodes, but the paratracheal nodes are commonly involved. P...
[ "[MF8Y] Other specified clinical findings in specimens from the urinary system\n --PARENT--> [?] Clinical findings in specimens from the urinary system\n --CHILD--> [MF80] Diffuse mesangial sclerosis\n Def: Diffuse mesangial sclerosis is a histological appearance which is characterised by diffuse thickening of basement membrane and massive enlargement of mesangial areas leading to contraction and scleros...", "[MF8Y] Other specified clinical findings in specimens from the urinary system\n --PARENT--> [?] Clinical findings in specimens from the urinary system\n --PARENT--> [?] Symptoms, signs or clinical findings of the genitourinary system", "[4B20.Z] Sarcoidosis, unspecified\n --PARENT--> [4B20] Sarcoidosis\n Def: Sarcoidosis is a multisystem disorder of unknown cause characterised by the formation of immune granulomas in involved organs. The lung and the lymphatic system are predominantly affected, but virtual...\n --CHILD--> [4B20.2] Sarcoidosis of the digestive system\n Def: This is a syndrome involving abnormal collections of chronic inflammatory cells (granulomas) that can form as nodules in the digestive system....", "[4B20.Z] Sarcoidosis, unspecified\n --PARENT--> [4B20] Sarcoidosis\n Def: Sarcoidosis is a multisystem disorder of unknown cause characterised by the formation of immune granulomas in involved organs. The lung and the lymphatic system are predominantly affected, but virtual...\n --CHILD--> [4B20.1] Sarcoidosis of lymph nodes\n Def: Lymphadenopathy is very common in sarcoidosis. Intrathoracic nodes are enlarged in 75 to 90% of all patients; usually this involves the hilar nodes, but the paratracheal nodes are commonly involved. P...", "[4B20.Y] Other specified sarcoidosis\n --PARENT--> [4B20] Sarcoidosis\n Def: Sarcoidosis is a multisystem disorder of unknown cause characterised by the formation of immune granulomas in involved organs. The lung and the lymphatic system are predominantly affected, but virtual...\n --CHILD--> [4B20.1] Sarcoidosis of lymph nodes\n Def: Lymphadenopathy is very common in sarcoidosis. Intrathoracic nodes are enlarged in 75 to 90% of all patients; usually this involves the hilar nodes, but the paratracheal nodes are commonly involved. P...", "[4B20.Y] Other specified sarcoidosis\n --PARENT--> [4B20] Sarcoidosis\n Def: Sarcoidosis is a multisystem disorder of unknown cause characterised by the formation of immune granulomas in involved organs. The lung and the lymphatic system are predominantly affected, but virtual...\n --CHILD--> [4B20.1] Sarcoidosis of lymph nodes\n Def: Lymphadenopathy is very common in sarcoidosis. Intrathoracic nodes are enlarged in 75 to 90% of all patients; usually this involves the hilar nodes, but the paratracheal nodes are commonly involved. P..." ]
MF8Y
Other specified clinical findings in specimens from the urinary system
[ { "from_icd11": "4B20.Z", "icd10_code": "D8689", "icd10_title": "Sarcoidosis of other sites" }, { "from_icd11": "4B20.Z", "icd10_code": "D8685", "icd10_title": "Sarcoid myocarditis" }, { "from_icd11": "4B20.Z", "icd10_code": "D8686", "icd10_title": "Sarcoid arthropathy" }, { "from_icd11": "4B20.Z", "icd10_code": "D8682", "icd10_title": "Multiple cranial nerve palsies in sarcoidosis" }, { "from_icd11": "4B20.Z", "icd10_code": "D8683", "icd10_title": "Sarcoid iridocyclitis" }, { "from_icd11": "4B20.Z", "icd10_code": "D8687", "icd10_title": "Sarcoid myositis" }, { "from_icd11": "4B20.Z", "icd10_code": "D8681", "icd10_title": "Sarcoid meningitis" }, { "from_icd11": "4B20.Z", "icd10_code": "D869", "icd10_title": "Sarcoidosis, unspecified" }, { "from_icd11": "4B20.Z", "icd10_code": "D86", "icd10_title": "Sarcoidosis" }, { "from_icd11": "4B20.Z", "icd10_code": "D868", "icd10_title": "Sarcoidosis of other sites" }, { "from_icd11": "4B20.5", "icd10_code": "D863", "icd10_title": "Sarcoidosis of skin" }, { "from_icd11": "4B20.0", "icd10_code": "D860", "icd10_title": "Sarcoidosis of lung" }, { "from_icd11": "3A51.1", "icd10_code": "D571", "icd10_title": "Sickle-cell disease without crisis" } ]
D8689
Sarcoidosis of other sites
The diagnosis were cerebral cysticercosis, symptomatic epilepsy and encephalatrophy. The patient had a history of cerebral cysticercosis and had been considered to have a ‘Herxheimer reaction’ after a significant worsening of headache symptoms at the beginning of treatment. T. solium was detected by CSF tNGS, and the diagnosis of cerebral cysticercosis was clear. According to the American Journal of Heat Disease (New Year’s Edition 48), Albendazole (15 mg/kg/d), praziquantel (50 mg/kg/d), and dexamethasone (0.1 mg/kg/d) were administered for 10 days, with glucocorticosteroids initiated 1 day prior to antiparasite treatment ( 1 ). The patient was administered oral albendazole at a dose of 0.2 g once daily for 3 days. Throughout the treatment, the patient experienced no exacerbation of headache, no rash, and no fever. Hence the patient was treated with albendazole at a dosage of 0.4 g three times a day orally, in combination with prednisone acetate at 50 mg once a day for a duration of 10 days. Following this period, prednisone acetate was gradually tapered off, while albendazole at 0.4 g three times a day continued for an additional 7 days. To control seizures, the patient was administered oxcarbazepine at a dosage of 0.15 g twice daily orally. Following the treatment, the patient’s condition stabilized, with no reported headaches, seizure-related limb shaking, slurred speech, or facial drooping.
3.964844
0.972656
sec[1]/p[5]
en
0.999996
40313611
https://doi.org/10.3389/fneur.2025.1504348
[ "albendazole", "cerebral", "cysticercosis", "headache", "daily", "three", "times", "orally", "prednisone", "acetate" ]
[ { "code": "1D00.Z", "title": "Infectious encephalitis, unspecified" }, { "code": "8E7Y", "title": "Other specified diseases of the nervous system" }, { "code": "8B20", "title": "Stroke not known if ischaemic or haemorrhagic" }, { "code": "8B1Z", "title": "Cerebral ischaemia, unspecified" }, { "code": "8B11.5Z", "title": "Cerebral ischaemic stroke, unspecified" }, { "code": "1F70.Z", "title": "Cysticercosis, unspecified" }, { "code": "1F70.Y", "title": "Other specified cysticercosis" }, { "code": "1F70.1", "title": "Cysticercosis of eye" }, { "code": "1F70.0Z", "title": "Cysticercosis of central nervous system, unspecified" }, { "code": "9A21.Y&XN8XE", "title": "Cysticercosis of orbit" } ]
=== ICD-11 CODES FOUND === [1D00.Z] Infectious encephalitis, unspecified Also known as: Infectious encephalitis, unspecified | Infectious encephalitis, not elsewhere classified | encephalitis NOS | acute encephalitis NOS | acute brain inflammation [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 [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 [8B1Z] Cerebral ischaemia, unspecified Also known as: Cerebral ischaemia, unspecified | brain ischaemia | cerebrovascular ischaemic disease | cerebrovascular ischaemia | cerebral anaemia [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 [1F70.Z] Cysticercosis, unspecified Also known as: Cysticercosis, unspecified | Cysticercosis | cysticerciasis infection due to larval form of Taenia solium [1F70.Y] Other specified cysticercosis Also known as: Other specified cysticercosis | Cysticercosis of the intestine [1F70.1] Cysticercosis of eye Definition: A disease of the eye, caused by an infection of tissue with larval cysts from the parasitic worm Taenia solium. This disease is characterised by cysts floating in the vitreous humour of the eye leading to impaired vision. Transmission is by haematogenous spread of larvae to the eye after ingestion of Taenia solium eggs in contaminated food or water. Confirmation is commonly by history of travel in parasite endemic regions and advanced imaging of the eye. Also known as: Cysticercosis of eye | Endophthalmitis in cysticercosis of eye [1F70.0Z] Cysticercosis of central nervous system, unspecified Also known as: Cysticercosis of central nervous system, unspecified | Cysticercosis of central nervous system | cerebral cysticercosis | neurocysticercosis | brain cysticercosis === GRAPH WALKS === --- Walk 1 --- [1D00.Z] Infectious encephalitis, unspecified --PARENT--> [1D00] Infectious encephalitis, not elsewhere classified Def: A disease of the brain, caused by an infection.... --CHILD--> [1D00.1] Fungal encephalitis --- Walk 2 --- [1D00.Z] Infectious encephalitis, unspecified --PARENT--> [1D00] Infectious encephalitis, not elsewhere classified Def: A disease of the brain, caused by an infection.... --CHILD--> [1D00.0] Bacterial encephalitis --- Walk 3 --- [8E7Y] Other specified diseases of the nervous system --PARENT--> [08] Diseases of the nervous system Def: This is a group of conditions characterised as being in or associated with the nervous system.... --RELATED_TO--> [?] Structural developmental anomalies of the nervous system Def: Any condition caused by failure of the nervous system to correctly develop during the antenatal period.... --- Walk 4 --- [8E7Y] Other specified diseases of the nervous system --PARENT--> [08] Diseases of the nervous system Def: This is a group of conditions characterised as being in or associated with the nervous system.... --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 5 --- [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 6 --- [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...
[ "[1D00.Z] Infectious encephalitis, unspecified\n --PARENT--> [1D00] Infectious encephalitis, not elsewhere classified\n Def: A disease of the brain, caused by an infection....\n --CHILD--> [1D00.1] Fungal encephalitis", "[1D00.Z] Infectious encephalitis, unspecified\n --PARENT--> [1D00] Infectious encephalitis, not elsewhere classified\n Def: A disease of the brain, caused by an infection....\n --CHILD--> [1D00.0] Bacterial encephalitis", "[8E7Y] Other specified diseases of the nervous system\n --PARENT--> [08] Diseases of the nervous system\n Def: This is a group of conditions characterised as being in or associated with the nervous system....\n --RELATED_TO--> [?] Structural developmental anomalies of the nervous system\n Def: Any condition caused by failure of the nervous system to correctly develop during the antenatal period....", "[8E7Y] Other specified diseases of the nervous system\n --PARENT--> [08] Diseases of the nervous system\n Def: This is a group of conditions characterised as being in or associated with the nervous system....\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....", "[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..." ]
1D00.Z
Infectious encephalitis, unspecified
[ { "from_icd11": "1D00.Z", "icd10_code": "G0490", "icd10_title": "Encephalitis and encephalomyelitis, unspecified" }, { "from_icd11": "1D00.Z", "icd10_code": "G0491", "icd10_title": "Myelitis, unspecified" }, { "from_icd11": "1D00.Z", "icd10_code": "G0430", "icd10_title": "Acute necrotizing hemorrhagic encephalopathy, unspecified" }, { "from_icd11": "1D00.Z", "icd10_code": "G0431", "icd10_title": "Postinfectious acute necrotizing hemorrhagic encephalopathy" }, { "from_icd11": "1D00.Z", "icd10_code": "G0439", "icd10_title": "Other acute necrotizing hemorrhagic encephalopathy" }, { "from_icd11": "1D00.Z", "icd10_code": "G0481", "icd10_title": "Other encephalitis and encephalomyelitis" }, { "from_icd11": "1D00.Z", "icd10_code": "G0489", "icd10_title": "Other myelitis" }, { "from_icd11": "1D00.Z", "icd10_code": "G04", "icd10_title": "Encephalitis, myelitis and encephalomyelitis" }, { "from_icd11": "1D00.Z", "icd10_code": "G048", "icd10_title": "Other encephalitis, myelitis and encephalomyelitis" }, { "from_icd11": "8B20", "icd10_code": "I64", "icd10_title": "" }, { "from_icd11": "8B1Z", "icd10_code": "I67848", "icd10_title": "Other cerebrovascular vasospasm and vasoconstriction" }, { "from_icd11": "8B1Z", "icd10_code": "I6789", "icd10_title": "Other cerebrovascular disease" }, { "from_icd11": "8B1Z", "icd10_code": "I6782", "icd10_title": "Cerebral ischemia" }, { "from_icd11": "8B1Z", "icd10_code": "I6781", "icd10_title": "Acute cerebrovascular insufficiency" }, { "from_icd11": "8B1Z", "icd10_code": "I67841", "icd10_title": "Reversible cerebrovascular vasoconstriction syndrome" } ]
G0490
Encephalitis and encephalomyelitis, unspecified
At 31 weeks of gestation, the patient suddenly had chest tightness, a temperature of 37.6 °C, nausea, headache, chest pain with breathing, and a cough with white foam sputum. She vomited 1 time and had concomitant back pain. MRI examination showed that there was no obvious abnormality in the brain. Echocardiography showed that the hyperechoic mass at the beginning of the left pulmonary artery was significantly smaller than that at the previous time (13 mm * 8 mm) and that the mass swung with the cardiac cycle. There is no obvious reduction of the mitral valve vegetation (18 mm * 7 mm, posterior leaflet; 11 mm*7 mm, anterior leaflet) . Furthermore, the blood picture indexes, except for procalcitonin, were significantly increased. If we were to consider a monistic explanation wherein a small bacterial embolus was shed, a cerebral infarction could not be completely ruled out, even though it was not indicated by the MRI. Thus, an emergency cesarean section was performed, and a live male baby was delivered in the cephalic position, with a weight of 2160 g, a length of 43 cm, and an Apgar score of 10 points. Fig. 3 a Echocardiography at 31 weeks of gestation shows that the vegetation has shrunk. b No obvious reduction of mitral valve vegetation. (PA = pulmonary artery; PDA = patent ductus arteriosus; RPA = right pulmonary artery; DAO = descending aorta; green arrow = infective endocarditis vegetative)
3.861328
0.983398
sec[1]/p[3]
en
0.999996
32448305
https://doi.org/10.1186/s13019-020-01147-6
[ "that", "obvious", "pulmonary", "artery", "vegetation", "gestation", "chest", "pain", "time", "echocardiography" ]
[ { "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": "6D50", "title": "Factitious disorder imposed on self" }, { "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" } ]
=== 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 [6D50] Factitious disorder imposed on self Definition: Factitious disorder imposed on self is characterised by feigning, falsifying, or inducing medical, psychological, or behavioural signs and symptoms or injury associated with identified deception. If a pre-existing disorder or disease is present, the individual intentionally aggravates existing symptoms or falsifies or induces additional symptoms. The individual seeks treatment or otherwise presents himself or herself as ill, injured, or impaired based on the feigned, falsified, or self-induced s Also known as: Factitious disorder imposed on self | artificial factitious disease | feigned disorder without obvious motivation | factitious disturbance | factitious disorder, not otherwise specified Includes: Münchhausen syndrome Excludes: Excoriation disorder | Malingering [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 === 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... --PARENT--> [?] Headache disorders --- 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... --CHILD--> [8A80.0] Migraine without aura Def: Recurrent headache disorder manifesting in attacks lasting 4-72 hours. The duration of attacks may be shorter in children. Typical characteristics of the headache are unilateral location, pulsating qu... --- 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.... --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 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--> [PL13.1] Underdosing, 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--> [PL13.1] Underdosing, 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 --PARENT--> [?] Headache disorders", "[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 --CHILD--> [8A80.0] Migraine without aura\n Def: Recurrent headache disorder manifesting in attacks lasting 4-72 hours. The duration of attacks may be shorter in children. Typical characteristics of the headache are unilateral location, pulsating qu...", "[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 --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", "[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--> [PL13.1] Underdosing, 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--> [PL13.1] Underdosing, 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
After the aortic clamp was released, sinus rhythm was restored spontaneously at a rate of 120 to 130 beats per minute and the electrocardiogram showed ST segment elevation. Intravenous infusions of epinephrine and nitroglycerin were administered at a dose of 0.05 μg/(kg·min) and 0.5 μg/(kg·min), respectively. When bypass withdrawal was attempted, sustained hypotension and low saturation of blood oxygen occurred. The systolic blood pressure ranged between 40 ~ 50 mmHg and a SpO 2 value at the finger could not be detected. An oximetry probe was attached to the ear of the infant for SpO2 monitoring, but no signal was detectable. The arterial blood gas analysis revealed a PaO 2 of 35.4 mmHg, PaCO 2 of 43.2 mmHg Hb and a hemoglobin concentration of 100.5 g/L. There was severe myocardial edema and this made the size of the heart exceed the pericardial cavity. The rate of the epinephrine intravenous infusion was increased to 0.1 μg/(kg·min), but no significant increase in blood pressure occurred. A systolic blood pressure below 50 mmHg is insufficient for satisfactory perfusion of body organs. As CPB had been completed and the aortic cannula removed, pressure detection at aortic root was not performed. Cerebral oximetry (Engin Bio-medical Electronics Co., Ltd., Suzhou, China) was applied to the left side to evaluate cerebral perfusion and revealed a cerebral tissue oxygen saturation (SctO 2 ) of 35.7%.
4.078125
0.893066
sec[1]/p[2]
en
0.999996
32593285
https://doi.org/10.1186/s12871-020-01071-1
[ "blood", "pressure", "mmhg", "aortic", "cerebral", "intravenous", "epinephrine", "saturation", "oxygen", "occurred" ]
[ { "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": "EH90.Z", "title": "Pressure ulcer of unspecified grade" }, { "code": "MB23.L", "title": "Pressured speech" }, { "code": "MD30.Z", "title": "Chest pain, unspecified" }, { "code": "CB22.Y", "title": "Other specified diseases of mediastinum, not elsewhere classified" }, { "code": "BA2Z", "title": "Hypotension, 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 [EH90.Z] Pressure ulcer of unspecified grade Also known as: Pressure ulcer of unspecified grade | Pressure ulceration | pressure injury | pressure ulcer | decubitus ulcer [MB23.L] Pressured speech Definition: Speech in which the person feels undue pressure to get the words out. The person’s speech is usually rapid, loud, and emphatic and may be difficult or impossible to interrupt. Frequently, the person talks without any social stimulation and may continue to talk even though no one is listening. Also known as: Pressured speech Excludes: Schizophrenia or other primary psychotic disorders | Bipolar or related disorders [MD30.Z] Chest pain, unspecified Also known as: Chest pain, unspecified | Pain in throat or chest | chest pain NOS | pain in chest | chest pressure [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 [BA2Z] Hypotension, unspecified Also known as: Hypotension, unspecified | hypopiesis | low blood pressure | arterial hypotension NOS | decreased blood pressure === 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--> [?] 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 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--> [MF50.4Z] Haematuria, unspecified --- 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--> [MF50.40] Macroscopic haematuria --- 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--> [MA12.0] Finding of opiate drug 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 --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....", "[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--> [MF50.4Z] Haematuria, unspecified", "[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--> [MF50.40] Macroscopic haematuria", "[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", "[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
Since December 2019, coronavirus disease (COVID-19), caused by a novel coronavirus named severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), emerged in Wuhan, Hubei province, China, and spread worldwide. Due to the reduced accessibility of cancer care services caused by the COVID-19 pandemic, cancer patients have been suffering from dual anxiety due to SARS-CoV-2 infection and cancer progression. Reports of COVID-19 in cancer patients have been limited so far, and most studies have focused mainly on the epidemiological and clinical features of the infection ( 1 – 3 ). To the best of our knowledge, cases of cancer patients who contracted COVID-19 during chemotherapy or radiotherapy have not been reported in detail. Nasopharyngeal cancer patients deserve more attention since the nasopharyngeal cavity is a crucial pathway by which this respiratory virus invades the lungs and is the primary reservoir of SARS-CoV-2 ( 4 ). Due to the potential adverse effects of chemo/radiotherapy on immunity, there is growing fear of receiving treatment among cancer patients. Therefore, more accurate reports from the frontlines are valuable to policy makers and oncologists alike. Herein, we report the case of a nasopharyngeal cancer patient who contracted COVID-19 during radiochemotherapy and has since recovered from the infection. The case occurred in Wuhan, the original epicenter of the outbreak in China.
4.046875
0.838867
sec[0]/p[0]
en
0.999997
33194574
https://doi.org/10.3389/fonc.2020.01755
[ "cancer", "covid", "patients", "since", "coronavirus", "sars", "infection", "nasopharyngeal", "caused", "respiratory" ]
[ { "code": "2D4Z", "title": "Unspecified malignant neoplasms of unspecified sites" }, { "code": "2C0Z", "title": "Malignant neoplasms of intestine, unspecified" }, { "code": "2B5Z", "title": "Malignant mesenchymal neoplasm of unspecified type" }, { "code": "2E2Z", "title": "Malignant neoplasm metastasis, unspecified" }, { "code": "2D42", "title": "Malignant neoplasms of ill-defined sites" }, { "code": "RA01.0", "title": "COVID-19, virus identified" }, { "code": "RA02", "title": "Post COVID-19 condition" }, { "code": "RA01", "title": "COVID-19" }, { "code": "RA01.1", "title": "COVID-19, virus not identified" }, { "code": "QA08.5", "title": "Special screening examination for other viral diseases" } ]
=== ICD-11 CODES FOUND === [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 [2C0Z] Malignant neoplasms of intestine, unspecified Also known as: Malignant neoplasms of intestine, unspecified | cancer of intestine | malignant neoplasm of intestine NOS | malignant tumour of intestine NOS | intestinal cancer NOS [2B5Z] Malignant mesenchymal neoplasm of unspecified type Also known as: Malignant mesenchymal neoplasm of unspecified type | calvarium cancer | ethmoid bone cancer | facial bone cancer | frontal bone cancer [2E2Z] Malignant neoplasm metastasis, unspecified Also known as: Malignant neoplasm metastasis, unspecified | secondary malignant neoplasm | metastasis | metastases | disseminated metastases [2D42] Malignant neoplasms of ill-defined sites Definition: 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. Also known as: Malignant neoplasms of ill-defined sites | Malignant neoplasm of ill-defined site of head, face or neck | Malignant neoplasm of nose NOS | Primary malignant neoplasm of cheek | malignant neoplasm of cheek NOS [RA01.0] COVID-19, virus identified Also known as: COVID-19, virus identified | 2019-new Coronavirus acute respiratory disease (deprecated) | 2019-nCoV acute respiratory disease [temporary name] (deprecated) | Coronavirus disease 2019 | SARS-CoV-2 disease Includes: Coronavirus disease 2019 | COVID-19 NOS Excludes: Coronavirus infection, unspecified site | Middle East respiratory syndrome | Severe acute respiratory syndrome [RA02] Post COVID-19 condition Definition: Post COVID-19 condition occurs in individuals with a history of probable or confirmed SARS CoV-2 infection, usually 3 months from the onset of COVID-19 with symptoms, and that last for at least 2 months and cannot be explained by an alternative diagnosis. Common symptoms include fatigue, shortness of breath, cognitive dysfunction but also others, and generally have an impact on everyday functioning. Symptoms may be new onset following initial recovery from an acute COVID-19 episode or persist fr Also known as: Post COVID-19 condition | postCOVID condition | post-COVID-19 condition | long COVID [RA01] COVID-19 Definition: As definition may evolve, the URL for the Global surveillance document will be added as the short description Also known as: COVID-19 [RA01.1] COVID-19, virus not identified Also known as: COVID-19, virus not identified | clinically diagnosed COVID-19 | suspected COVID-19 | probable COVID-19 | clinical COVID-19 Excludes: COVID-19, virus identified | Coronavirus infection, unspecified site | Special screening examination for other viral diseases [QA08.5] Special screening examination for other viral diseases Also known as: Special screening examination for other viral diseases | Measles screening | Poliomyelitis screening | Rubella screening | Screening for Dengue fever Includes: Screening for COVID-19 Excludes: Viral intestinal infections | Special screening examination for infections with a predominantly sexual mode of transmission | Special screening examination for human immunodeficiency virus === GRAPH WALKS === --- Walk 1 --- [2D4Z] Unspecified malignant neoplasms of unspecified sites --PARENT--> [?] Malignant neoplasms of ill-defined or unspecified primary sites --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 2 --- [2D4Z] Unspecified malignant neoplasms of unspecified sites --PARENT--> [?] Malignant neoplasms of ill-defined or unspecified primary sites --CHILD--> [2D41] Unspecified carcinoma of unspecified site --- Walk 3 --- [2C0Z] Malignant neoplasms of intestine, unspecified --PARENT--> [?] Malignant neoplasms of intestine --CHILD--> [2B80] Malignant neoplasms of small intestine Def: A primary malignant neoplasm involving the small intestine.... --- Walk 4 --- [2C0Z] Malignant neoplasms of intestine, unspecified --PARENT--> [?] Malignant neoplasms of intestine --CHILD--> [?] Malignant neoplasms of large intestine --- Walk 5 --- [2B5Z] Malignant mesenchymal neoplasm of unspecified type --PARENT--> [?] 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... --CHILD--> [2B50] Chondrosarcoma, primary site --- Walk 6 --- [2B5Z] Malignant mesenchymal neoplasm of unspecified type --PARENT--> [?] 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... --CHILD--> [2B52] Ewing sarcoma, primary site Def: A small round cell tumour that lacks morphologic, immunohistochemical, and electron microscopic evidence of neuroectodermal differentiation. It represents one of the two ends of the spectrum called Ew...
[ "[2D4Z] Unspecified malignant neoplasms of unspecified sites\n --PARENT--> [?] Malignant neoplasms of ill-defined or unspecified primary sites\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...", "[2D4Z] Unspecified malignant neoplasms of unspecified sites\n --PARENT--> [?] Malignant neoplasms of ill-defined or unspecified primary sites\n --CHILD--> [2D41] Unspecified carcinoma of unspecified site", "[2C0Z] Malignant neoplasms of intestine, unspecified\n --PARENT--> [?] Malignant neoplasms of intestine\n --CHILD--> [2B80] Malignant neoplasms of small intestine\n Def: A primary malignant neoplasm involving the small intestine....", "[2C0Z] Malignant neoplasms of intestine, unspecified\n --PARENT--> [?] Malignant neoplasms of intestine\n --CHILD--> [?] Malignant neoplasms of large intestine", "[2B5Z] Malignant mesenchymal neoplasm of unspecified type\n --PARENT--> [?] 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...\n --CHILD--> [2B50] Chondrosarcoma, primary site", "[2B5Z] Malignant mesenchymal neoplasm of unspecified type\n --PARENT--> [?] 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...\n --CHILD--> [2B52] Ewing sarcoma, primary site\n Def: A small round cell tumour that lacks morphologic, immunohistochemical, and electron microscopic evidence of neuroectodermal differentiation. It represents one of the two ends of the spectrum called Ew..." ]
2D4Z
Unspecified malignant neoplasms of unspecified sites
[ { "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" }, { "from_icd11": "2D4Z", "icd10_code": "C801", "icd10_title": "Malignant (primary) neoplasm, unspecified" }, { "from_icd11": "2D4Z", "icd10_code": "C768", "icd10_title": "Malignant neoplasm of other specified ill-defined sites" }, { "from_icd11": "2D4Z", "icd10_code": "C761", "icd10_title": "Malignant neoplasm of thorax" }, { "from_icd11": "2D4Z", "icd10_code": "C762", "icd10_title": "Malignant neoplasm of abdomen" }, { "from_icd11": "2D4Z", "icd10_code": "C763", "icd10_title": "Malignant neoplasm of pelvis" }, { "from_icd11": "2D4Z", "icd10_code": "C800", "icd10_title": "Disseminated malignant neoplasm, unspecified" }, { "from_icd11": "2D4Z", "icd10_code": "C76-C80", "icd10_title": "" }, { "from_icd11": "2D4Z", "icd10_code": "C76", "icd10_title": "Malignant neoplasm of other and ill-defined sites" } ]
C802
Malignant neoplasm associated with transplanted organ
She was transferred to our hospital on the 17th day, and was scheduled to undergo a semi-radical surgery for the malignant ovarian tumor on the 31st day (1 month) after the cerebral infarction. To reduce the relative risk of pulmonary embolism, a temporary inferior vena cava (IVC) filter (Denali™ Vena Cava Filter, BD, Franklin Lakes, NJ, US) was placed on the 2nd day after admission. Both edoxaban and cilostazol were discontinued 5 days preceding surgery, and intravenous (IV) infusion of unfractionated heparin was initiated on the next day. Preoperative electrocardiogram showed regular sinus tachycardia. Transthoracic echocardiography (TTE) and carotid artery echography did not detect causative embolic sources or abnormalities such as an intracardiac right to left shunt. Blood test results the day before surgery were not remarkable except activated partial thromboplastin time (APTT) of 40 sec, fibrinogen of 656 mg/dL, and D-dimer of 1.4 μg/mL. Heparinization was terminated 6 h prior to surgery. In addition to standard monitoring, we observed depth of anesthesia (BIS™, Medtronic, Minneapolis, MN, USA), and regional cerebral oxygen saturation levels during anesthesia. The baseline rSO 2 at room air was 58% and 66% on the right and left side of the forehead, respectively. Transesophageal echocardiography (TEE) was kept at hand in preparation for hemodynamic instabilities such as pulmonary embolism.
3.857422
0.97168
sec[1]/p[1]
en
0.999996
32388737
https://doi.org/10.1186/s40981-020-00339-2
[ "cerebral", "pulmonary", "embolism", "vena", "cava", "filter", "echocardiography", "anesthesia", "transferred", "scheduled" ]
[ { "code": "1D00.Z", "title": "Infectious encephalitis, unspecified" }, { "code": "8E7Y", "title": "Other specified diseases of the nervous system" }, { "code": "8B20", "title": "Stroke not known if ischaemic or haemorrhagic" }, { "code": "8B1Z", "title": "Cerebral ischaemia, unspecified" }, { "code": "8B11.5Z", "title": "Cerebral ischaemic stroke, unspecified" }, { "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" } ]
=== ICD-11 CODES FOUND === [1D00.Z] Infectious encephalitis, unspecified Also known as: Infectious encephalitis, unspecified | Infectious encephalitis, not elsewhere classified | encephalitis NOS | acute encephalitis NOS | acute brain inflammation [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 [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 [8B1Z] Cerebral ischaemia, unspecified Also known as: Cerebral ischaemia, unspecified | brain ischaemia | cerebrovascular ischaemic disease | cerebrovascular ischaemia | cerebral anaemia [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 [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 === GRAPH WALKS === --- Walk 1 --- [1D00.Z] Infectious encephalitis, unspecified --PARENT--> [1D00] Infectious encephalitis, not elsewhere classified Def: A disease of the brain, caused by an infection.... --CHILD--> [1D00.1] Fungal encephalitis --- Walk 2 --- [1D00.Z] Infectious encephalitis, unspecified --PARENT--> [1D00] Infectious encephalitis, not elsewhere classified Def: A disease of the brain, caused by an infection.... --CHILD--> [1D00.0] Bacterial encephalitis --- Walk 3 --- [8E7Y] Other specified diseases of the nervous system --PARENT--> [08] Diseases of the nervous system Def: This is a group of conditions characterised as being in or associated with the nervous system.... --RELATED_TO--> [?] Non-viral and unspecified infections of the central nervous system Def: Any condition of the nervous system, caused by an infection with a bacterial, fungal, parasitic or unspecified source.... --- Walk 4 --- [8E7Y] Other specified diseases of the nervous system --PARENT--> [08] Diseases of the nervous system Def: This is a group of conditions characterised as being in or associated with the nervous system.... --RELATED_TO--> [?] Non-viral and unspecified infections of the central nervous system Def: Any condition of the nervous system, caused by an infection with a bacterial, fungal, parasitic or unspecified source.... --- Walk 5 --- [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 6 --- [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...
[ "[1D00.Z] Infectious encephalitis, unspecified\n --PARENT--> [1D00] Infectious encephalitis, not elsewhere classified\n Def: A disease of the brain, caused by an infection....\n --CHILD--> [1D00.1] Fungal encephalitis", "[1D00.Z] Infectious encephalitis, unspecified\n --PARENT--> [1D00] Infectious encephalitis, not elsewhere classified\n Def: A disease of the brain, caused by an infection....\n --CHILD--> [1D00.0] Bacterial encephalitis", "[8E7Y] Other specified diseases of the nervous system\n --PARENT--> [08] Diseases of the nervous system\n Def: This is a group of conditions characterised as being in or associated with the nervous system....\n --RELATED_TO--> [?] Non-viral and unspecified infections of the central nervous system\n Def: Any condition of the nervous system, caused by an infection with a bacterial, fungal, parasitic or unspecified source....", "[8E7Y] Other specified diseases of the nervous system\n --PARENT--> [08] Diseases of the nervous system\n Def: This is a group of conditions characterised as being in or associated with the nervous system....\n --RELATED_TO--> [?] Non-viral and unspecified infections of the central nervous system\n Def: Any condition of the nervous system, caused by an infection with a bacterial, fungal, parasitic or unspecified source....", "[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..." ]
1D00.Z
Infectious encephalitis, unspecified
[ { "from_icd11": "1D00.Z", "icd10_code": "G0490", "icd10_title": "Encephalitis and encephalomyelitis, unspecified" }, { "from_icd11": "1D00.Z", "icd10_code": "G0491", "icd10_title": "Myelitis, unspecified" }, { "from_icd11": "1D00.Z", "icd10_code": "G0430", "icd10_title": "Acute necrotizing hemorrhagic encephalopathy, unspecified" }, { "from_icd11": "1D00.Z", "icd10_code": "G0431", "icd10_title": "Postinfectious acute necrotizing hemorrhagic encephalopathy" }, { "from_icd11": "1D00.Z", "icd10_code": "G0439", "icd10_title": "Other acute necrotizing hemorrhagic encephalopathy" }, { "from_icd11": "1D00.Z", "icd10_code": "G0481", "icd10_title": "Other encephalitis and encephalomyelitis" }, { "from_icd11": "1D00.Z", "icd10_code": "G0489", "icd10_title": "Other myelitis" }, { "from_icd11": "1D00.Z", "icd10_code": "G04", "icd10_title": "Encephalitis, myelitis and encephalomyelitis" }, { "from_icd11": "1D00.Z", "icd10_code": "G048", "icd10_title": "Other encephalitis, myelitis and encephalomyelitis" }, { "from_icd11": "8B20", "icd10_code": "I64", "icd10_title": "" }, { "from_icd11": "8B1Z", "icd10_code": "I67848", "icd10_title": "Other cerebrovascular vasospasm and vasoconstriction" }, { "from_icd11": "8B1Z", "icd10_code": "I6789", "icd10_title": "Other cerebrovascular disease" }, { "from_icd11": "8B1Z", "icd10_code": "I6782", "icd10_title": "Cerebral ischemia" }, { "from_icd11": "8B1Z", "icd10_code": "I6781", "icd10_title": "Acute cerebrovascular insufficiency" }, { "from_icd11": "8B1Z", "icd10_code": "I67841", "icd10_title": "Reversible cerebrovascular vasoconstriction syndrome" } ]
G0490
Encephalitis and encephalomyelitis, unspecified
She was diagnosed with infective endocarditis complicated with systemic multiple abscesses due to CA-MRSA and C. albicans . However, because of brain hemorrhage and low platelet count, primary surgical treatment was considered intolerable. Therefore, medical antibacterial treatment with fluconazole (FLCZ), meropenem (MEPM), and vancomycin (VCM) was introduced, and heart failure treatment with mechanical circulatory support and renal replacement therapy was continued . A steroid therapy was also introduced for the destructive thyroiditis. Hemodynamics were stabilized, and ECMO and IABP were weaned off on day 5 of admission. Renal function also normalized, and the renal replacement therapy could also be discontinued. The platelet counts gradually increased and reached 10.0 × 10 4 /µL, and surgical treatments were conducted on day 26 of admission after regression of cerebral hemorrhage was confirmed by brain CT scan . Fig. 3 Time course of multiple treatments, weight blood cell counts, serum C-reactive protein level, and the results of blood culture after admission. CHDF, continuous, hemodiafiltration; CRP, C-reactive protein; FLCZ, fluconazole; IABP, intra-arterial balloon pumping; MCFG, micafungin; MEPM, meropenem; MRSA, methicillin-resistant Staphylococcus aureus ; ST, trimethoprim-sulfamethoxazole; WBC, white blood cell; VA-ECMO, venoarterial extracorporeal membrane oxygenation; VCM, vancomycin
3.917969
0.967773
sec[1]/p[2]
en
0.999995
PMC11533610
https://doi.org/10.1186/s44215-023-00057-y
[ "renal", "blood", "multiple", "mrsa", "brain", "hemorrhage", "platelet", "fluconazole", "flcz", "meropenem" ]
[ { "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": "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 === [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 [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 --- [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 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--> [?] Renal failure following abortion, ectopic or molar pregnancy --- Walk 3 --- [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... --CHILD--> [?] Autosomal dominant polycystic kidney disease, Type 2 Def: Autosomal dominant polycystic kidney disease due to mutations on Polycystin2 gene on chromosome 4 (PKD1 gene).... --- 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... --CHILD--> [?] Autosomal dominant polycystic kidney disease type 1 without tuberous sclerosis Def: Autosomal dominant polycystic kidney disease due to mutations on Polycystin1 gene on chromosome 16 (PKD1 gene)... --- 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 --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....", "[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", "[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 --CHILD--> [?] Autosomal dominant polycystic kidney disease, Type 2\n Def: Autosomal dominant polycystic kidney disease due to mutations on Polycystin2 gene on chromosome 4 (PKD1 gene)....", "[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 --CHILD--> [?] Autosomal dominant polycystic kidney disease type 1 without tuberous sclerosis\n Def: Autosomal dominant polycystic kidney disease due to mutations on Polycystin1 gene on chromosome 16 (PKD1 gene)...", "[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": "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": "" } ]
N19
Unspecified kidney failure
He was then admitted with the chief complaint of decreased visual acuity in the right eye. Best corrected visual acuity (VA) was 20/200 in the right eye and 20/20 in the left eye. Intraocular pressure was 10 mmHg in the right eye and 18 mmHg in the left eye. Slit-lamp and fundoscopic examination of the right eye showed respectively anterior uveitis rated to 2+ for both anterior chamber cells and flare, according to the Standardization of Uveitis Nomenclature (SUN) guidelines and vitritis associated with large paravascular haemorrhages and yellow necrotic borders. The retinal lesion was located on the temporal superior vascular arcade and involved the posterior pole but not the fovea, which was confirmed by angiography . The left eye appeared normal. Both CMV DNA in serum and aqueous humor were positive (respectively 330,000 copies/mL and 76,000 copies/mL). There was no other tissue-invasive disease and no acute graft dysfunction. Fig. 1 a : Color fundus photograph of the right eye showing inflammation of the posterior chamber (vitritis) associated with large paravascular haemorrhages and yellow necrotic borders. b : Fluorescein angiography of the same eye showing hypofluorescence due to hemorrhages, and hyperfluorescence due to leakage. c : Evolution after 2 weeks: attenuation of vitritis, stabilization of retinitis. d : Evolution after 1 month: resolution of vitritis, stabilization of retinitis
3.986328
0.979492
sec[1]/p[9]
en
0.999996
33256663
https://doi.org/10.1186/s12886-020-01741-1
[ "vitritis", "visual", "acuity", "mmhg", "respectively", "uveitis", "both", "chamber", "associated", "large" ]
[ { "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" }, { "code": "9D94", "title": "Impairment of presenting visual acuity" }, { "code": "9D96", "title": "Impairment of uncorrected visual acuity" }, { "code": "9D95", "title": "Impairment of best corrected visual acuity" }, { "code": "JB0D.7", "title": "Failed application of vacuum extractor or forceps, unspecified" }, { "code": "9A96.Z", "title": "Anterior uveitis, unspecified" } ]
=== ICD-11 CODES FOUND === [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 [9D94] Impairment of presenting visual acuity Also known as: Impairment of presenting visual acuity [9D96] Impairment of uncorrected visual acuity Also known as: Impairment of uncorrected visual acuity [9D95] Impairment of best corrected visual acuity Also known as: Impairment of best corrected visual acuity [JB0D.7] Failed application of vacuum extractor or forceps, unspecified Also known as: Failed application of vacuum extractor or forceps, unspecified | Failed application of ventouse or forceps, with subsequent delivery by forceps or caesarean section respectively Includes: Failed application of ventouse or forceps, with subsequent delivery by forceps or caesarean section respectively [9A96.Z] Anterior uveitis, unspecified Also known as: Anterior uveitis, unspecified | Anterior uveitis | uveokeratitis | keratouveitis | iridocyclitis === GRAPH WALKS === --- Walk 1 --- [9E1Z] Diseases of the visual system, unspecified --PARENT--> [09] Diseases of the visual system Def: This refers to any diseases of the visual system, which includes the eyes and adnexa, the visual pathways and brain areas, which initiate and control visual perception and visually guided behaviour.... --RELATED_TO--> [?] Contusion of eyeball or orbital tissues Def: Injuries to the eyeball and surrounding tissue resulting in haemorrhage, usually manifested in the skin.... --- Walk 2 --- [9E1Z] Diseases of the visual system, unspecified --PARENT--> [09] Diseases of the visual system Def: This refers to any diseases of the visual system, which includes the eyes and adnexa, the visual pathways and brain areas, which initiate and control visual perception and visually guided behaviour.... --EXCLUDES--> [?] Certain infectious or parasitic diseases Def: This chapter includes certain conditions caused by pathogenic organisms or microorganisms, such as bacteria, viruses, parasites or fungi.... --- Walk 3 --- [MC1Y] Other specified symptoms or signs involving the visual system --PARENT--> [?] Symptoms or signs involving the visual system --CHILD--> [MC11] Eye sensation abnormal --- Walk 4 --- [MC1Y] Other specified symptoms or signs involving the visual system --PARENT--> [?] Symptoms or signs involving the visual system --RELATED_TO--> [?] Ophthalmoparesis Def: Paresis of one or more extraocular muscles... --- Walk 5 --- [9D9Z] Vision impairment, unspecified --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--> [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... --- Walk 6 --- [9D9Z] Vision impairment, unspecified --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... --PARENT--> [09] Diseases of the visual system Def: This refers to any diseases of the visual system, which includes the eyes and adnexa, the visual pathways and brain areas, which initiate and control visual perception and visually guided behaviour....
[ "[9E1Z] Diseases of the visual system, unspecified\n --PARENT--> [09] Diseases of the visual system\n Def: This refers to any diseases of the visual system, which includes the eyes and adnexa, the visual pathways and brain areas, which initiate and control visual perception and visually guided behaviour....\n --RELATED_TO--> [?] Contusion of eyeball or orbital tissues\n Def: Injuries to the eyeball and surrounding tissue resulting in haemorrhage, usually manifested in the skin....", "[9E1Z] Diseases of the visual system, unspecified\n --PARENT--> [09] Diseases of the visual system\n Def: This refers to any diseases of the visual system, which includes the eyes and adnexa, the visual pathways and brain areas, which initiate and control visual perception and visually guided behaviour....\n --EXCLUDES--> [?] Certain infectious or parasitic diseases\n Def: This chapter includes certain conditions caused by pathogenic organisms or microorganisms, such as bacteria, viruses, parasites or fungi....", "[MC1Y] Other specified symptoms or signs involving the visual system\n --PARENT--> [?] Symptoms or signs involving the visual system\n --CHILD--> [MC11] Eye sensation abnormal", "[MC1Y] Other specified symptoms or signs involving the visual system\n --PARENT--> [?] Symptoms or signs involving the visual system\n --RELATED_TO--> [?] Ophthalmoparesis\n Def: Paresis of one or more extraocular muscles...", "[9D9Z] Vision impairment, unspecified\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--> [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...", "[9D9Z] Vision impairment, unspecified\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 --PARENT--> [09] Diseases of the visual system\n Def: This refers to any diseases of the visual system, which includes the eyes and adnexa, the visual pathways and brain areas, which initiate and control visual perception and visually guided behaviour...." ]
9E1Z
Diseases of the visual system, unspecified
[ { "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" }, { "from_icd11": "9E1Z", "icd10_code": "H57812", "icd10_title": "Brow ptosis, left" }, { "from_icd11": "9E1Z", "icd10_code": "H5789", "icd10_title": "Other specified disorders of eye and adnexa" }, { "from_icd11": "9E1Z", "icd10_code": "H3550", "icd10_title": "Unspecified hereditary retinal dystrophy" }, { "from_icd11": "9E1Z", "icd10_code": "E7030", "icd10_title": "Albinism, unspecified" } ]
H5500
Unspecified nystagmus
Kermani et al. described in his retrospective study four cases of mucormycosis. The first case was a 3-year-old girl with poor overall health condition who had the infection as a picture of mastoiditis. It is worth noting that she developed an anaphylactic shock while on amphotericin B unlike our patient who tolerated the drug extremely well. Furthermore, she was operated on but died four days later due to complication of sepsis, lateral sinus thrombosis, and multiorgan failure . Compared to our patient, she had a very good postoperative course and was better with the combination therapy that we initiated and monitored closely with careful tittering. Kermani et al., in his second case, describe an 18-year-old male with type 1 DM. The patient with mucormycosis was found in his maxillary sinus, hard palate, and inflammation of the periorbital region as a picture of cellulitis. The patient was also started on amphotericin B with surgical curettage of the palatine lesion. His symptoms resolved after 9 months completely except persistent grade II facial palsy. Compared to our patient, the infection was found in the ear auricle where her facial palsy was completely resolved 2 months later. Lastly, the last two cases were in relatively older patients who were also type 1 DM of 24- and 77-year-old males. They had a similar course with amphotericin B, and their symptoms resolved completely in 10 months .
3.894531
0.718262
sec[2]/p[2]
en
0.999995
33954001
https://doi.org/10.1155/2021/6618191
[ "amphotericin", "resolved", "completely", "kermani", "four", "cases", "mucormycosis", "infection", "picture", "that" ]
[ { "code": "EM0Y", "title": "Other specified diseases of the skin" }, { "code": "9B10.20", "title": "Traumatic cataract" }, { "code": "KB23.1", "title": "Transient tachypnoea of newborn" }, { "code": "MB5Z", "title": "Paralytic symptoms, unspecified" }, { "code": "LB9B", "title": "Reduction defects of upper and lower limbs" }, { "code": "LA85.1", "title": "Transposition of the great arteries" }, { "code": "LD40.Y", "title": "Other specified complete trisomies of the autosomes" }, { "code": "9D90.6", "title": "Blindness" }, { "code": "LD50.Y", "title": "Other specified number anomalies of chromosome X" }, { "code": "NA82.4", "title": "Multiple fractures of ribs" } ]
=== ICD-11 CODES FOUND === [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 [9B10.20] Traumatic cataract Definition: Partial or complete opacity on or in the lens or capsule of one or both eyes, impairing vision or causing blindness. The many kinds of cataract are classified by their morphology (size, shape, location) or etiology (cause and time of occurrence) resulting from or following injury. Also known as: Traumatic cataract | rupture of lens NOS | Localised traumatic opacities | Partially resolved traumatic cataract | Total traumatic cataract [KB23.1] Transient tachypnoea of newborn Definition: Transient tachypnoea of newborn is usually a benign self-limiting illness of term and near-term infants demonstrating increased respiratory rate and requiring supplementary oxygen after birth. Also known as: Transient tachypnoea of newborn | idiopathic tachypnoea of newborn | rapid; respiratory, transient, of newborn | tachypnoea resolving about 6 hours postnatally | transitory tachypnoea of newborn [MB5Z] Paralytic symptoms, unspecified Also known as: Paralytic symptoms, unspecified | paralysis syndrome | incomplete paralysis | complete paralysis | paresis [LB9B] Reduction defects of upper and lower limbs Also known as: Reduction defects of upper and lower limbs | Tetraamelia | Total amelia | Split hand - split foot | Acheiropodia [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 [LD40.Y] Other specified complete trisomies of the autosomes Also known as: Other specified complete trisomies of the autosomes | Other complete trisomies | entire chromosome trisomy, meiotic nondisjunction | Other trisomy mosaicism | Whole chromosome trisomy, mosaicism disorder [9D90.6] Blindness Definition: The numerical definition used for WHO statistics refers to profound, near-total or total loss. The functional definition refers to individuals who have little or no residual vision and who have to rely predominantly on vision substitution skills, i.e. on using senses other than vision (Braille or talking books for reading, a long cane or guide dog for mobility, or touch for manipulation). Also known as: Blindness | acquired amaurosis | acquired blindness | amaurosis | blindness, both eyes Includes: visual impairment category 5 | visual impairment categories 4, 5, 6 in both eyes | visual impairment categories 4, 5, 6 in one eye and categories 1, 2, 3 or 9 in the other eye [LD50.Y] Other specified number anomalies of chromosome X Also known as: Other specified number anomalies of chromosome X | Female with more than three X chromosomes | abnormal female chromosomes, with more than three x chromosomes | Tetrasomy X | 48 xxxx syndrome [NA82.4] Multiple fractures of ribs Also known as: Multiple fractures of ribs | rib fractures | Multiple rib fractures, involving first rib | Multiple rib fractures, involving two ribs | Multiple rib fractures, involving three ribs === GRAPH WALKS === --- Walk 1 --- [EM0Y] Other specified diseases of the skin --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... --RELATED_TO--> [?] Neonatal phototherapy burn Def: Burn resulting from phototherapy administered to neonate, usually for the treatment of neonatal jaundice.... --- Walk 2 --- [EM0Y] Other specified diseases of the skin --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... --RELATED_TO--> [?] Neonatal phototherapy burn Def: Burn resulting from phototherapy administered to neonate, usually for the treatment of neonatal jaundice.... --- Walk 3 --- [9B10.20] Traumatic cataract Def: Partial or complete opacity on or in the lens or capsule of one or both eyes, impairing vision or causing blindness. The many kinds of cataract are classified by their morphology (size, shape, locatio... --PARENT--> [9B10.2] Certain specified cataracts Def: A cataract is clouding of the lens of the eye, which impedes the passage of light.... --PARENT--> [9B10] Cataract --- Walk 4 --- [9B10.20] Traumatic cataract Def: Partial or complete opacity on or in the lens or capsule of one or both eyes, impairing vision or causing blindness. The many kinds of cataract are classified by their morphology (size, shape, locatio... --PARENT--> [9B10.2] Certain specified cataracts Def: A cataract is clouding of the lens of the eye, which impedes the passage of light.... --CHILD--> [9B10.21] Diabetic cataract Def: This refers to an unspecified group of metabolic diseases in which a person has high blood sugar, either because the pancreas does not produce enough insulin, or because cells do not respond to the in... --- Walk 5 --- [KB23.1] Transient tachypnoea of newborn Def: Transient tachypnoea of newborn is usually a benign self-limiting illness of term and near-term infants demonstrating increased respiratory rate and requiring supplementary oxygen after birth.... --PARENT--> [KB23] Respiratory distress of newborn Def: A condition characterised by developmental insufficiency of surfactant associated proteins or surfactant production and structural immaturity in the lungs.... --CHILD--> [KB23.2] Respiratory instability of prematurity Def: Infant within the neonatal period who requires continued respiratory life support, including positive pressure ventilation and/or prolonged oxygen therapy, without a clear pathologic diagnosis. This m... --- Walk 6 --- [KB23.1] Transient tachypnoea of newborn Def: Transient tachypnoea of newborn is usually a benign self-limiting illness of term and near-term infants demonstrating increased respiratory rate and requiring supplementary oxygen after birth.... --PARENT--> [KB23] Respiratory distress of newborn Def: A condition characterised by developmental insufficiency of surfactant associated proteins or surfactant production and structural immaturity in the lungs.... --EXCLUDES--> [?] Respiratory failure of newborn Def: Acute or chronic respiratory failure in a newborn. Neonates in acute respiratory failure require respiratory support....
[ "[EM0Y] Other specified diseases of the skin\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...\n --RELATED_TO--> [?] Neonatal phototherapy burn\n Def: Burn resulting from phototherapy administered to neonate, usually for the treatment of neonatal jaundice....", "[EM0Y] Other specified diseases of the skin\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...\n --RELATED_TO--> [?] Neonatal phototherapy burn\n Def: Burn resulting from phototherapy administered to neonate, usually for the treatment of neonatal jaundice....", "[9B10.20] Traumatic cataract\n Def: Partial or complete opacity on or in the lens or capsule of one or both eyes, impairing vision or causing blindness. The many kinds of cataract are classified by their morphology (size, shape, locatio...\n --PARENT--> [9B10.2] Certain specified cataracts\n Def: A cataract is clouding of the lens of the eye, which impedes the passage of light....\n --PARENT--> [9B10] Cataract", "[9B10.20] Traumatic cataract\n Def: Partial or complete opacity on or in the lens or capsule of one or both eyes, impairing vision or causing blindness. The many kinds of cataract are classified by their morphology (size, shape, locatio...\n --PARENT--> [9B10.2] Certain specified cataracts\n Def: A cataract is clouding of the lens of the eye, which impedes the passage of light....\n --CHILD--> [9B10.21] Diabetic cataract\n Def: This refers to an unspecified group of metabolic diseases in which a person has high blood sugar, either because the pancreas does not produce enough insulin, or because cells do not respond to the in...", "[KB23.1] Transient tachypnoea of newborn\n Def: Transient tachypnoea of newborn is usually a benign self-limiting illness of term and near-term infants demonstrating increased respiratory rate and requiring supplementary oxygen after birth....\n --PARENT--> [KB23] Respiratory distress of newborn\n Def: A condition characterised by developmental insufficiency of surfactant associated proteins or surfactant production and structural immaturity in the lungs....\n --CHILD--> [KB23.2] Respiratory instability of prematurity\n Def: Infant within the neonatal period who requires continued respiratory life support, including positive pressure ventilation and/or prolonged oxygen therapy, without a clear pathologic diagnosis. This m...", "[KB23.1] Transient tachypnoea of newborn\n Def: Transient tachypnoea of newborn is usually a benign self-limiting illness of term and near-term infants demonstrating increased respiratory rate and requiring supplementary oxygen after birth....\n --PARENT--> [KB23] Respiratory distress of newborn\n Def: A condition characterised by developmental insufficiency of surfactant associated proteins or surfactant production and structural immaturity in the lungs....\n --EXCLUDES--> [?] Respiratory failure of newborn\n Def: Acute or chronic respiratory failure in a newborn. Neonates in acute respiratory failure require respiratory support...." ]
EM0Y
Other specified diseases of the skin
[ { "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": "9B10.20", "icd10_code": "H26109", "icd10_title": "Unspecified traumatic cataract, unspecified eye" }, { "from_icd11": "9B10.20", "icd10_code": "H261", "icd10_title": "Traumatic cataract" }, { "from_icd11": "KB23.1", "icd10_code": "P221", "icd10_title": "Transient tachypnea of newborn" }, { "from_icd11": "MB5Z", "icd10_code": "G8384", "icd10_title": "Todd's paralysis (postepileptic)" }, { "from_icd11": "MB5Z", "icd10_code": "G8331", "icd10_title": "Monoplegia, unspecified affecting right dominant side" }, { "from_icd11": "MB5Z", "icd10_code": "G8389", "icd10_title": "Other specified paralytic syndromes" }, { "from_icd11": "MB5Z", "icd10_code": "G8383", "icd10_title": "Posterior cord syndrome" }, { "from_icd11": "MB5Z", "icd10_code": "G8381", "icd10_title": "Brown-Sequard syndrome" }, { "from_icd11": "MB5Z", "icd10_code": "G8382", "icd10_title": "Anterior cord syndrome" }, { "from_icd11": "MB5Z", "icd10_code": "G8332", "icd10_title": "Monoplegia, unspecified affecting left dominant side" }, { "from_icd11": "MB5Z", "icd10_code": "G8334", "icd10_title": "Monoplegia, unspecified affecting left nondominant side" }, { "from_icd11": "MB5Z", "icd10_code": "G8330", "icd10_title": "Monoplegia, unspecified affecting unspecified side" }, { "from_icd11": "MB5Z", "icd10_code": "G839", "icd10_title": "Paralytic syndrome, unspecified" } ]
L918
Other hypertrophic disorders of the skin
A 31-year-old man received a haplo-HSCT with sequential conditioning to treat a diffuse large B-cell lymphoma. Outcomes, drug treatments, and biological screening for infections after the HSCT are reported in Figure 1 . After 30 days post-transplant, we observed a complete (100%) donor chimerism. He developed an acute cutaneous graft versus host disease (GVHD) (stage I, grade I) treated with topical corticosteroids. Due to the occurrence of a severe (stage III) digestive GVHD, a high dose of corticosteroids (2 mg/kg) and ruloxitinib (10 mg twice a day) were started. Ruloxitinib was rapidly stopped due to thrombopenia. Due to corticosteroids resistance, ciclosporin was introduced two months post-transplant and allowed complete remission of cutaneous and digestive GVHD. Maintenance corticosteroids (0.5 mg/kg per day) were continued. During the 3 months post-transplant, the patient was screened with polymerase chain reaction (PCR) in peripheral blood (PB) every 1–2 weeks for cytomegalovirus (CMV), Epstein–Barr virus (EBV), and HAdV as recommended. All CMV and HAdV PCRs remained negative. Recurrent EBV DNA-emia was observed and treated by two rituximab administrations, leading to a significant decrease in viral load. Among further post-allograft infections, we noticed genital herpes and a Bacteroides uniformis bacteremia, which were treated by acyclovir and amoxicillin/clavulanic acid, respectively.
4.089844
0.96582
sec[1]/p[0]
en
0.999996
33804012
https://doi.org/10.3390/pathogens10030340
[ "corticosteroids", "transplant", "gvhd", "treated", "hsct", "infections", "complete", "cutaneous", "stage", "digestive" ]
[ { "code": "EE40.32", "title": "Purpura or bruising due to vascular fragility" }, { "code": "EE40.0", "title": "Corticosteroid-induced skin atrophy" }, { "code": "9C61.2A", "title": "Glaucoma due to drugs" }, { "code": "EE40.1Y", "title": "Stretch marks of other specified aetiology" }, { "code": "NE60", "title": "Harmful effects of drugs, medicaments or biological substances, not elsewhere classified" }, { "code": "QB63.Z", "title": "Presence of transplanted organ or tissue, unspecified" }, { "code": "QB63.Y", "title": "Presence of other transplanted organ or tissue" }, { "code": "NE84", "title": "Failure or rejection of transplanted organs or tissues" }, { "code": "QB63.4", "title": "Presence of transplanted skin" }, { "code": "QE00", "title": "Acculturation difficulty" } ]
=== ICD-11 CODES FOUND === [EE40.32] Purpura or bruising due to vascular fragility Definition: Purpura due to leakage or rupture of abnormally fragile cutaneous blood vessels. Also known as: Purpura or bruising due to vascular fragility | Senile purpura | Actinic purpura | Corticosteroid-induced purpura | Purpura or bruising due to genetically-determined skin fragility Includes: Senile purpura | Corticosteroid-induced purpura | Purpura or bruising due to genetically-determined skin fragility [EE40.0] Corticosteroid-induced skin atrophy Also known as: Corticosteroid-induced skin atrophy [9C61.2A] Glaucoma due to drugs Also known as: Glaucoma due to drugs | Glaucoma secondary to drugs | Corticosteroid-induced glaucoma | corticosteroid glaucoma | steroid-induced glaucoma [EE40.1Y] Stretch marks of other specified aetiology Also known as: Stretch marks of other specified aetiology | Pubertal stretch marks | Pubertal striae distensae | Obesity-related stretch marks | Striae distensae due to obesity [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 [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 [QB63.Y] Presence of other transplanted organ or tissue Also known as: Presence of other transplanted organ or tissue | Presence of transplanted heart and lungs | heart and lungs transplant status | Presence of transplanted intestine | intestinal transplant [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 [QB63.4] Presence of transplanted skin Also known as: Presence of transplanted skin | skin transplant status | autogenous skin transplant status | skin transplantation [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 === GRAPH WALKS === --- Walk 1 --- [EE40.32] Purpura or bruising due to vascular fragility Def: Purpura due to leakage or rupture of abnormally fragile cutaneous blood vessels.... --PARENT--> [EE40.3] Skin fragility Def: Fragility of the skin due principally to genetic or acquired abnormalities of dermal matrix proteins.... --CHILD--> [EE40.30] Genetically-determined skin fragility --- Walk 2 --- [EE40.32] Purpura or bruising due to vascular fragility Def: Purpura due to leakage or rupture of abnormally fragile cutaneous blood vessels.... --RELATED_TO--> [?] Scorbutic purpura Def: Scorbutic purpura is a cutaneous haemorrhagic manifestation of scurvy with petechial exanthema and ecchymosis at pressure points. They are secondary to defective formation of connective tissues and co... --PARENT--> [?] Purpura or bruising due to vascular fragility Def: Purpura due to leakage or rupture of abnormally fragile cutaneous blood vessels.... --- Walk 3 --- [EE40.0] Corticosteroid-induced skin atrophy --PARENT--> [EE40] Atrophy or degeneration of dermal or subcutaneous connective tissue Def: A heterogeneous group of disorders resulting from atrophic and degenerative changes in dermal and subcutaneous collagen and elastin.... --CHILD--> [EE40.1] Stretch marks Def: Linear scars attributable to rupture of the normal dermal matrix from distension by abnormal physical forces (pregnancy, obesity, pubertal growth spurt), increased collagenase activity (corticosteroid... --- Walk 4 --- [EE40.0] Corticosteroid-induced skin atrophy --PARENT--> [EE40] Atrophy or degeneration of dermal or subcutaneous connective tissue Def: A heterogeneous group of disorders resulting from atrophic and degenerative changes in dermal and subcutaneous collagen and elastin.... --CHILD--> [EE40.2] Atrophic scarring of the skin Def: The process whereby healing of damaged skin results in a reduction of dermal thickness as well as scarring, thus the counterpart of hypertrophic scarring.... --- Walk 5 --- [9C61.2A] Glaucoma due to drugs --PARENT--> [9C61.2] Secondary open-angle glaucoma --RELATED_TO--> [?] Glaucoma due to ocular surgery or laser --- Walk 6 --- [9C61.2A] Glaucoma due to drugs --PARENT--> [9C61.2] Secondary open-angle glaucoma --CHILD--> [9C61.20] Pseudoexfoliative open-angle glaucoma Def: Pseudoexfoliative Open-Angle glaucoma is a condition where fibrillar pseudoexfoliative material is produced by various ocular tissues and is deposited on the trabecular meshwork, lens, and other struc...
[ "[EE40.32] Purpura or bruising due to vascular fragility\n Def: Purpura due to leakage or rupture of abnormally fragile cutaneous blood vessels....\n --PARENT--> [EE40.3] Skin fragility\n Def: Fragility of the skin due principally to genetic or acquired abnormalities of dermal matrix proteins....\n --CHILD--> [EE40.30] Genetically-determined skin fragility", "[EE40.32] Purpura or bruising due to vascular fragility\n Def: Purpura due to leakage or rupture of abnormally fragile cutaneous blood vessels....\n --RELATED_TO--> [?] Scorbutic purpura\n Def: Scorbutic purpura is a cutaneous haemorrhagic manifestation of scurvy with petechial exanthema and ecchymosis at pressure points. They are secondary to defective formation of connective tissues and co...\n --PARENT--> [?] Purpura or bruising due to vascular fragility\n Def: Purpura due to leakage or rupture of abnormally fragile cutaneous blood vessels....", "[EE40.0] Corticosteroid-induced skin atrophy\n --PARENT--> [EE40] Atrophy or degeneration of dermal or subcutaneous connective tissue\n Def: A heterogeneous group of disorders resulting from atrophic and degenerative changes in dermal and subcutaneous collagen and elastin....\n --CHILD--> [EE40.1] Stretch marks\n Def: Linear scars attributable to rupture of the normal dermal matrix from distension by abnormal physical forces (pregnancy, obesity, pubertal growth spurt), increased collagenase activity (corticosteroid...", "[EE40.0] Corticosteroid-induced skin atrophy\n --PARENT--> [EE40] Atrophy or degeneration of dermal or subcutaneous connective tissue\n Def: A heterogeneous group of disorders resulting from atrophic and degenerative changes in dermal and subcutaneous collagen and elastin....\n --CHILD--> [EE40.2] Atrophic scarring of the skin\n Def: The process whereby healing of damaged skin results in a reduction of dermal thickness as well as scarring, thus the counterpart of hypertrophic scarring....", "[9C61.2A] Glaucoma due to drugs\n --PARENT--> [9C61.2] Secondary open-angle glaucoma\n --RELATED_TO--> [?] Glaucoma due to ocular surgery or laser", "[9C61.2A] Glaucoma due to drugs\n --PARENT--> [9C61.2] Secondary open-angle glaucoma\n --CHILD--> [9C61.20] Pseudoexfoliative open-angle glaucoma\n Def: Pseudoexfoliative Open-Angle glaucoma is a condition where fibrillar pseudoexfoliative material is produced by various ocular tissues and is deposited on the trabecular meshwork, lens, and other struc..." ]
EE40.32
Purpura or bruising due to vascular fragility
[ { "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
Further CT scan showed that the thickened soft tissue in the anterior mediastinum almost disappeared 3 months after ASCT , while an anterior mediastinal mass was detected again 6 months after ASCT , suggesting a potential recurrence of the original lesion. On January 31, 2018, a multi-disciplinary team (MDT), composed of specialists from the Imaging Department (including the specialists from the PET center), Thoracic Surgery Department and the Hematology, was built to make a discussion regarding the condition of the patient. They thought the anterior mediastinal mass was unknown and might be thymus tissue or tumor tissue, and a further observation or a biopsy was required to define. Following another discussion regarding the condition, a video-assisted thoracoscopic surgery was performed for biopsy of the soft tissue of the anterior mediastinum for pathological examination and the result showed thymus tissue . Final chest CT scan 12 months after ASCT showed an anterior mediastinal mass similar to that on the previous chest CT image . The patient has achieved disease-free survival so far. The timeline of the patient is shown in Additional file 1 . Fig. 2 The results of anterior mediastinal biopsy in patients suggested that the thymus tissue. Figure 2 Shows thymus lobule structure, fat hyperplasia and separation, left superior cortex lymphocyte rich (HE staining [h e matoxylin–eosin staining] 100)
3.898438
0.958984
sec[1]/p[3]
en
0.999995
33446156
https://doi.org/10.1186/s12893-021-01048-y
[ "tissue", "mediastinal", "thymus", "that", "asct", "biopsy", "scan", "soft", "mediastinum", "specialists" ]
[ { "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" }, { "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 === [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 [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 --- [FB6Z] Soft tissue disorders, unspecified --PARENT--> [?] Soft tissue disorders --CHILD--> [?] Disorders of muscles --- Walk 2 --- [FB6Z] Soft tissue disorders, unspecified --PARENT--> [?] Soft tissue disorders --CHILD--> [?] Miscellaneous specified soft tissue disorders Def: This is a group of other disorders, which are not defined elsewhere, affecting tissues that connect, support, or surround other structures and organs of the body, not being bone.... --- Walk 3 --- [MC85] Gangrene Def: Gangrene, not elsewhere classified is the death of tissues in the body which happens when a part of the body loses its blood supply.... --EXCLUDES--> [?] Gas gangrene Def: Gas gangrene or clostridial myonecrosis is a potentially fatal, rapidly progressive necrotizing infection of muscle and soft tissue resulting from bacterial invasion of healthy muscle from adjacent tr... --PARENT--> [?] Other bacterial diseases --- Walk 4 --- [MC85] Gangrene Def: Gangrene, not elsewhere classified is the death of tissues in the body which happens when a part of the body loses its blood supply.... --EXCLUDES--> [?] Pyoderma gangrenosum Def: An idiopathic, rapidly evolving, and severely debilitating disease occurring most commonly in association with chronic ulcerative colitis. It is characterised by the presence of boggy, purplish ulcers... --CHILD--> [?] Pyoderma gangrenosum classified by clinical type --- Walk 5 --- [FB56.6] Other specified soft tissue disorders --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--> [?] Radiculopathy --- Walk 6 --- [FB56.6] Other specified soft tissue disorders --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.... --CHILD--> [FB56.0] Foreign body granuloma of soft tissue, not elsewhere classified
[ "[FB6Z] Soft tissue disorders, unspecified\n --PARENT--> [?] Soft tissue disorders\n --CHILD--> [?] Disorders of muscles", "[FB6Z] Soft tissue disorders, unspecified\n --PARENT--> [?] Soft tissue disorders\n --CHILD--> [?] Miscellaneous specified soft tissue disorders\n Def: This is a group of other disorders, which are not defined elsewhere, affecting tissues that connect, support, or surround other structures and organs of the body, not being bone....", "[MC85] Gangrene\n Def: Gangrene, not elsewhere classified is the death of tissues in the body which happens when a part of the body loses its blood supply....\n --EXCLUDES--> [?] Gas gangrene\n Def: Gas gangrene or clostridial myonecrosis is a potentially fatal, rapidly progressive necrotizing infection of muscle and soft tissue resulting from bacterial invasion of healthy muscle from adjacent tr...\n --PARENT--> [?] Other bacterial diseases", "[MC85] Gangrene\n Def: Gangrene, not elsewhere classified is the death of tissues in the body which happens when a part of the body loses its blood supply....\n --EXCLUDES--> [?] Pyoderma gangrenosum\n Def: An idiopathic, rapidly evolving, and severely debilitating disease occurring most commonly in association with chronic ulcerative colitis. It is characterised by the presence of boggy, purplish ulcers...\n --CHILD--> [?] Pyoderma gangrenosum classified by clinical type", "[FB56.6] Other specified soft tissue disorders\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--> [?] Radiculopathy", "[FB56.6] Other specified soft tissue disorders\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 --CHILD--> [FB56.0] Foreign body granuloma of soft tissue, not elsewhere classified" ]
FB6Z
Soft tissue disorders, unspecified
[ { "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" }, { "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" } ]
M60-M79
Skin lesions appeared as early as the first day of life as numerous papulo-vesicular lesions, which became generalized during the following days requiring admission into pediatric intensive care unit. These lesions have been nearly continuously present, with exacerbations, occasionally hemorrhagic and complicated with infections, ulcerated lesions, and ulcerative granulomata . In recent years, large areas of cutis laxa and hyperpigmentation were detected . At 2.5 years of age, bilateral conjunctivitis, corneal erosions, and nodules appeared . Fig. 2 Description of cutaneous, pulmonary, and ocular inflammatory manifestations in patients. Panel a Multiple papules and serosal and hemorrhagic vesicles on the hands and palms detected in patient 1 at the age of 4 years. Panel b Large areas of cutis laxa in the abdominal region detected in patient 1 at the age of 7 years. Panels c, d Ocular inflammatory lesions including intense bilateral conjunctivitis, keratitis, episcleritis, and nodules in the sclera detected over the course of the disease in patient 1. Panel e Bronchiectasis detected in patient 1. Panel f Blistering inflammatory cutaneous lesions in the leg detected in patient 2 at the age of 6 months. Panel g Areas of cutis laxa detected in patient 2 at the age of 6 years. Panel h Ocular inflammatory lesions including conjunctivitis and corneal limbitis detected in patient 2 at the age of 7 years
3.935547
0.625977
sec[2]/sec[0]/sec[0]/p[1]
en
0.999996
32671674
https://doi.org/10.1007/s10875-020-00794-7
[ "lesions", "panel", "inflammatory", "areas", "cutis", "laxa", "conjunctivitis", "ocular", "appeared", "hemorrhagic" ]
[ { "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": "FA2Z", "title": "Inflammatory arthropathies, unspecified" }, { "code": "FB84.Z", "title": "Osteomyelitis or osteitis, unspecified" }, { "code": "8C1Z", "title": "Mononeuropathy of unspecified site" }, { "code": "BD90.Z", "title": "Lymphadenitis, unspecified" }, { "code": "FB55.Z", "title": "Enthesopathies, unspecified" } ]
=== 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 [FA2Z] Inflammatory arthropathies, unspecified Also known as: Inflammatory arthropathies, unspecified | polyarthritis NOS | inflammatory joint disease NOS | nonpyogenic arthritis NOS | arthritic nodosa [FB84.Z] Osteomyelitis or osteitis, unspecified Also known as: Osteomyelitis or osteitis, unspecified | Osteomyelitis or osteitis | bone inflammation | bone ulcer | bone inflammatory disease [8C1Z] Mononeuropathy of unspecified site Also known as: Mononeuropathy of unspecified site | inflammation of nerve NOS | nerve condition NOS | neuritis NOS | nerve disease NOS [BD90.Z] Lymphadenitis, unspecified Also known as: Lymphadenitis, unspecified | Lymphadenitis | adenitis NOS | inflammation of gland | lymphatic gland inflammation [FB55.Z] Enthesopathies, unspecified Also known as: Enthesopathies, unspecified | Certain specified enthesopathies | Enthesopathy of elbow | enthesopathy of elbow region | Adhesive capsulitis not elsewhere classified === GRAPH WALKS === --- Walk 1 --- [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 2 --- [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 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.... --CHILD--> [?] Conditions associated with the spine Def: This is a group of conditions in which there is a deviation from or interruption of the normal structure or function of the spine.... --- 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--> [?] Nonorgan specific systemic autoimmune disorders --- 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--> [?] 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...", "[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 ...", "[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 --CHILD--> [?] Conditions associated with the spine\n Def: This is a group of conditions in which there is a deviation from or interruption of the normal structure or function of the spine....", "[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", "[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": "FA2Z", "icd10_code": "M1389", "icd10_title": "Other specified arthritis, multiple sites" }, { "from_icd11": "FA2Z", "icd10_code": "M1380", "icd10_title": "Other specified arthritis, unspecified site" }, { "from_icd11": "FA2Z", "icd10_code": "M13862", "icd10_title": "Other specified arthritis, left knee" }, { "from_icd11": "FA2Z", "icd10_code": "M13872", "icd10_title": "Other specified arthritis, left ankle and foot" }, { "from_icd11": "FA2Z", "icd10_code": "M13871", "icd10_title": "Other specified arthritis, right ankle and foot" }, { "from_icd11": "FA2Z", "icd10_code": "M13861", "icd10_title": "Other specified arthritis, right knee" }, { "from_icd11": "FA2Z", "icd10_code": "M13879", "icd10_title": "Other specified arthritis, unspecified ankle and foot" }, { "from_icd11": "FA2Z", "icd10_code": "M13842", "icd10_title": "Other specified arthritis, left hand" }, { "from_icd11": "FA2Z", "icd10_code": "M13841", "icd10_title": "Other specified arthritis, right hand" }, { "from_icd11": "FA2Z", "icd10_code": "M13811", "icd10_title": "Other specified arthritis, right shoulder" } ]
M00-M25
A 67-year-old female patient with a history of glaucoma and left fallopian tube serous adenocarcinoma status post total abdominal hysterectomy and right salpingo-oophorectomy presented with symptoms of lower GI bleeding and anemia for which she underwent colonoscopy. Her family history was positive for endometrial cancer in her sister, and genetic studies showed mutations in mismatch repair genes suggestive of hereditary non-polyposis colorectal cancer (Lynch syndrome - MLH1/MSH2/MSH6/PMS2). Immunohistochemistry of the fallopian tube tumor was positive for Ber-Ep4, EMA, and WT1. It was negative for calretinin with some cells positive for estrogen receptor (ER) immunostain (consistent with high-grade serous adenocarcinoma of Müllerian origin). Colonoscopy revealed that the patient had a proximal transverse colon mass, which appeared as a primary colon malignant mass . Assuming this was primary colon malignancy, she underwent right hemicolectomy with the intraoperative presence of enlarged lymphatics along the ileocolic trunk. She had elevated CA-125 levels, and carcinoembryonic antigen levels were within normal limits. Pathology showed poorly differentiated carcinoma involving right pericolic adipose tissue suggestive of primary fallopian cancer origin. The patient was discharged in stable condition and placed on gemcitabine chemotherapy after this for which she completed three out of six cycles.
3.986328
0.981445
sec[1]/p[0]
en
0.999998
32953309
https://doi.org/10.7759/cureus.9795
[ "fallopian", "which", "cancer", "colon", "tube", "serous", "adenocarcinoma", "colonoscopy", "suggestive", "origin" ]
[ { "code": "JA01.1", "title": "Tubal pregnancy" }, { "code": "GA1Z&XA3EF0", "title": "Noninflammatory disorders of fallopian tube" }, { "code": "GA07.Z&XA3EF0", "title": "Inflammatory disease of fallopian tube" }, { "code": "GA31.01", "title": "Primary female infertility of tubal origin" }, { "code": "GA17.Y", "title": "Other specified acquired abnormalities of fallopian tube" }, { "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": "2D4Z", "title": "Unspecified malignant neoplasms of unspecified sites" } ]
=== 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 [GA31.01] Primary female infertility of tubal origin Definition: Female infertility caused by dysfunction of one or both fallopian tubes, usually related to pelvic adhesions or occurring after pelvic surgery, with or without hydrosalpinx Also known as: Primary female infertility of tubal origin | infertility of tubal origin NOS | Fallopian tube occlusion | blocked fallopian tube | fallopian tube obstruction [GA17.Y] Other specified acquired abnormalities of fallopian tube Also known as: Other specified acquired abnormalities of fallopian tube | Diverticulum of fallopian tube | Infarction of fallopian tube | Cyst of fallopian tube, not elsewhere classified | oviduct cyst [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 [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 === 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--> [JA01.1] Tubal pregnancy Def: A condition characterised by implantation of the embryo within the fallopian tube (ampullary, isthmus, interstitium) 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.... --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 3 --- [GA31.01] Primary female infertility of tubal origin Def: Female infertility caused by dysfunction of one or both fallopian tubes, usually related to pelvic adhesions or occurring after pelvic surgery, with or without hydrosalpinx... --PARENT--> [GA31.0] Primary female infertility Def: Infertility in a woman who has never had a clinical pregnancy... --PARENT--> [GA31] Female infertility Def: Disease of the reproductive system defined by the failure to achieve a clinical pregnancy after 12 months or more of regular unprotected sexual intercourse.... --- Walk 4 --- [GA31.01] Primary female infertility of tubal origin Def: Female infertility caused by dysfunction of one or both fallopian tubes, usually related to pelvic adhesions or occurring after pelvic surgery, with or without hydrosalpinx... --PARENT--> [GA31.0] Primary female infertility Def: Infertility in a woman who has never had a clinical pregnancy... --CHILD--> [GA31.00] Primary female infertility of uterine origin Def: Female infertility caused by uterine abnormalities on the level of the endometrium or myometrium, with more detailed description classified elsewhere, i.e. under genitourinary infections, STDs and non... --- Walk 5 --- [GA17.Y] Other specified acquired abnormalities of fallopian tube --PARENT--> [GA17] Acquired abnormalities of fallopian tube Def: A condition of the fallopian tube, caused by determinants arising after birth. This condition is characterised by a malfunction, malformation, or another anomaly.... --PARENT--> [?] Noninflammatory disorders of female genital tract Def: Any disorder of the female genital tract, characterised by pathological changes, leading to noninflammatory effects.... --- Walk 6 --- [GA17.Y] Other specified acquired abnormalities of fallopian tube --PARENT--> [GA17] Acquired abnormalities of fallopian tube Def: A condition of the fallopian tube, caused by determinants arising after birth. This condition is characterised by a malfunction, malformation, or another anomaly.... --PARENT--> [?] Noninflammatory disorders of female genital tract Def: Any disorder of the female genital tract, characterised by pathological changes, leading to noninflammatory effects....
[ "[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--> [JA01.1] Tubal pregnancy\n Def: A condition characterised by implantation of the embryo within the fallopian tube (ampullary, isthmus, interstitium) 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 --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....", "[GA31.01] Primary female infertility of tubal origin\n Def: Female infertility caused by dysfunction of one or both fallopian tubes, usually related to pelvic adhesions or occurring after pelvic surgery, with or without hydrosalpinx...\n --PARENT--> [GA31.0] Primary female infertility\n Def: Infertility in a woman who has never had a clinical pregnancy...\n --PARENT--> [GA31] Female infertility\n Def: Disease of the reproductive system defined by the failure to achieve a clinical pregnancy after 12 months or more of regular unprotected sexual intercourse....", "[GA31.01] Primary female infertility of tubal origin\n Def: Female infertility caused by dysfunction of one or both fallopian tubes, usually related to pelvic adhesions or occurring after pelvic surgery, with or without hydrosalpinx...\n --PARENT--> [GA31.0] Primary female infertility\n Def: Infertility in a woman who has never had a clinical pregnancy...\n --CHILD--> [GA31.00] Primary female infertility of uterine origin\n Def: Female infertility caused by uterine abnormalities on the level of the endometrium or myometrium, with more detailed description classified elsewhere, i.e. under genitourinary infections, STDs and non...", "[GA17.Y] Other specified acquired abnormalities of fallopian tube\n --PARENT--> [GA17] Acquired abnormalities of fallopian tube\n Def: A condition of the fallopian tube, caused by determinants arising after birth. This condition is characterised by a malfunction, malformation, or another anomaly....\n --PARENT--> [?] Noninflammatory disorders of female genital tract\n Def: Any disorder of the female genital tract, characterised by pathological changes, leading to noninflammatory effects....", "[GA17.Y] Other specified acquired abnormalities of fallopian tube\n --PARENT--> [GA17] Acquired abnormalities of fallopian tube\n Def: A condition of the fallopian tube, caused by determinants arising after birth. This condition is characterised by a malfunction, malformation, or another anomaly....\n --PARENT--> [?] Noninflammatory disorders of female genital tract\n Def: Any disorder of the female genital tract, characterised by pathological changes, leading to noninflammatory effects...." ]
JA01.1
Tubal pregnancy
[ { "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": "GA31.01", "icd10_code": "N971", "icd10_title": "Female infertility of tubal origin" }, { "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": "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" } ]
O00102
Left tubal pregnancy without intrauterine pregnancy
She received 60 Gy delivered in 30 fractions to her primary and mediastinal nodal disease with intensity modulated radiation therapy prescribed to the 90% isodose line with concurrent cisplatin and etoposide. The planning treatment volume received a maximum dose of 66.7 Gy and a mean dose of 63.8 Gy. The volume of uninvolved lung receiving greater than or equal to 20 Gy (V20Gy) was 22%. The ipsilateral left main stem and branches of the bronchus were within the planning treatment volume and received full dose . She tolerated therapy well with only grade one dermatitis, fatigue, and pneumonitis. Two months after chemoradiotherapy, the patient underwent thoracotomy, left upper lobectomy, mediastinal lymph node dissection, and intercostal muscle flap buttress to the bronchial stump. Postsurgical pathology revealed pathologic complete response to neoadjuvant therapy, with no tumor detected in the left upper lobe or dissected lymph nodes. She recovered from surgery without complications and was discharged after 3 days. Throughout the next 2 years, CT surveillance scans were performed and notable for apical postradiation fibrosis. The patient continued to smoke. Figure 2 Intensity modulated radiation therapy treatment plan. Radiation plan of the left upper lobe and mediastinal adenocarcinoma with representative coronal plane. Prescription dose was 60 Gy in 2 Gy fractions to the 90% isodose line. Fig 2
3.927734
0.964844
sec[2]/p[0]
en
0.999995
34761140
https://doi.org/10.1016/j.adro.2021.100811
[ "mediastinal", "radiation", "fractions", "intensity", "modulated", "isodose", "line", "planning", "lymph", "lobe" ]
[ { "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" }, { "code": "NF00", "title": "Effects of radiation, not elsewhere classified" }, { "code": "QC48.Y", "title": "Other specified personal history of medical treatment" }, { "code": "EK90.Y", "title": "Other discrete epidermal dysplasias" }, { "code": "CA82.1", "title": "Chronic or other pulmonary manifestations due to radiation" }, { "code": "DA25.32", "title": "Radiation oesophageal ulcer" } ]
=== ICD-11 CODES FOUND === [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 [NF00] Effects of radiation, not elsewhere classified Also known as: Effects of radiation, not elsewhere classified | radiation complications | infrared rays injury | Radiation sickness Excludes: Sunburn | Burns | specified adverse effects of radiation, such as leukaemia [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 [EK90.Y] Other discrete epidermal dysplasias Also known as: Other discrete epidermal dysplasias | Actinic cheilitis | Photochemotherapy-induced keratosis | Thermal keratosis | Chronic radiation keratosis [CA82.1] Chronic or other pulmonary manifestations due to radiation Definition: A chronic inflammatory reaction of the lung ultimately resulting in fibrosis in response to repeated or high dose radiation exposure. Also known as: Chronic or other pulmonary manifestations due to radiation | Fibrosis of lung following radiation | radiation fibrosis of lung | Chronic radiation pulmonary fibrosis [DA25.32] Radiation oesophageal ulcer Also known as: Radiation oesophageal ulcer === GRAPH WALKS === --- Walk 1 --- [CB22.Z] Disease of mediastinum, unspecified --PARENT--> [CB22] Diseases of mediastinum, not elsewhere classified Def: This refers to diseases of the mediastinum where the mediastinum is an undelineated group of structures in the thorax, surrounded by loose connective tissue. It is the central compartment of the thora... --CHILD--> [CB22.Z] Disease of mediastinum, unspecified --- Walk 2 --- [CB22.Z] Disease of mediastinum, unspecified --PARENT--> [CB22] Diseases of mediastinum, not elsewhere classified Def: This refers to diseases of the mediastinum where the mediastinum is an undelineated group of structures in the thorax, surrounded by loose connective tissue. It is the central compartment of the thora... --CHILD--> [CB22.Z] Disease of mediastinum, unspecified --- Walk 3 --- [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--> [?] Influenza Def: Any disease of the respiratory system, caused by an infection with influenza virus. These diseases are characterised by fever, cough, headache, myalgia, arthralgia, or malaise. Transmission is by inha... --- Walk 4 --- [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... --- Walk 5 --- [CB22.Y] Other specified diseases of mediastinum, not elsewhere classified --PARENT--> [CB22] Diseases of mediastinum, not elsewhere classified Def: This refers to diseases of the mediastinum where the mediastinum is an undelineated group of structures in the thorax, surrounded by loose connective tissue. It is the central compartment of the thora... --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... --- Walk 6 --- [CB22.Y] Other specified diseases of mediastinum, not elsewhere classified --PARENT--> [CB22] Diseases of mediastinum, not elsewhere classified Def: This refers to diseases of the mediastinum where the mediastinum is an undelineated group of structures in the thorax, surrounded by loose connective tissue. It is the central compartment of the thora... --CHILD--> [CB22.Z] Disease of mediastinum, unspecified
[ "[CB22.Z] Disease of mediastinum, unspecified\n --PARENT--> [CB22] Diseases of mediastinum, not elsewhere classified\n Def: This refers to diseases of the mediastinum where the mediastinum is an undelineated group of structures in the thorax, surrounded by loose connective tissue. It is the central compartment of the thora...\n --CHILD--> [CB22.Z] Disease of mediastinum, unspecified", "[CB22.Z] Disease of mediastinum, unspecified\n --PARENT--> [CB22] Diseases of mediastinum, not elsewhere classified\n Def: This refers to diseases of the mediastinum where the mediastinum is an undelineated group of structures in the thorax, surrounded by loose connective tissue. It is the central compartment of the thora...\n --CHILD--> [CB22.Z] Disease of mediastinum, unspecified", "[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--> [?] Influenza\n Def: Any disease of the respiratory system, caused by an infection with influenza virus. These diseases are characterised by fever, cough, headache, myalgia, arthralgia, or malaise. Transmission is by inha...", "[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...", "[CB22.Y] Other specified diseases of mediastinum, not elsewhere classified\n --PARENT--> [CB22] Diseases of mediastinum, not elsewhere classified\n Def: This refers to diseases of the mediastinum where the mediastinum is an undelineated group of structures in the thorax, surrounded by loose connective tissue. It is the central compartment of the thora...\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...", "[CB22.Y] Other specified diseases of mediastinum, not elsewhere classified\n --PARENT--> [CB22] Diseases of mediastinum, not elsewhere classified\n Def: This refers to diseases of the mediastinum where the mediastinum is an undelineated group of structures in the thorax, surrounded by loose connective tissue. It is the central compartment of the thora...\n --CHILD--> [CB22.Z] Disease of mediastinum, unspecified" ]
CB22.Z
Disease of mediastinum, unspecified
[ { "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" }, { "from_icd11": "NF00", "icd10_code": "T66XXXA", "icd10_title": "Radiation sickness, unspecified, initial encounter" }, { "from_icd11": "NF00", "icd10_code": "T66XXXS", "icd10_title": "Radiation sickness, unspecified, sequela" }, { "from_icd11": "NF00", "icd10_code": "T66", "icd10_title": "Radiation sickness, unspecified" }, { "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" } ]
J9859
Other diseases of mediastinum, not elsewhere classified
In January 2013, a 49-year-old male (Patient #1) was admitted to the University Medical Center Hamburg-Eppendorf due to progressive visual problems. He reported a prior episode of similar symptoms with spontaneous recovery 10 months earlier. He had a medical history of systemic sarcoidosis (Stage II = lymphadenopathy and parenchymal disease), histologically proven by a mediastinal lymph node biopsy in 2001, which led to a treatment with corticosteroids for 18 months . However, he was not taking any immunosuppressive medication at the time of developing neurological symptoms in 2012 and 2013. Neurological examination revealed a Balint’s syndrome, which consists of simultanagnosia, optic ataxia and oculomotor apraxia. Cranial MRI showed increased signal intensities in T 2 -weighted scans in the parietooccipital area and in the inner capsule and no gadolinium enhancement in T 1 -weighted scans . CSF analysis revealed an elevated protein level of 721 mg l −1 without pathological cell counts or isolated oligoclonal bands. PCR analysis for JCV DNA in the CSF was negative (detection limit 100 copies ml −1 ). Due to the rapid progression of neurological symptoms with enlarging lesions and hemiparesis, a brain biopsy was performed in April 2013 leading to the diagnosis of PML . Repeated analysis of the CSF for JCV DNA by PCR confirmed the diagnosis with 20 copies ml −1 (detection limit 10 copies ml −1 ).
4.113281
0.964844
sec[2]/sec[0]/p[0]
en
0.999998
34993476
https://doi.org/10.1093/braincomms/fcab292
[ "neurological", "copies", "biopsy", "which", "weighted", "scans", "detection", "limit", "january", "university" ]
[ { "code": "QF10", "title": "Limited function or disability of body organ or system" }, { "code": "6B60.Z", "title": "Dissociative neurological symptom disorder, with unspecified symptoms" }, { "code": "8D43.Z", "title": "Neurological disorders due to toxicity, unspecified" }, { "code": "8D43.Y", "title": "Other specified neurological disorders due to toxicity" }, { "code": "MD93", "title": "Dysphagia" }, { "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" } ]
=== ICD-11 CODES FOUND === [QF10] Limited function or disability of body organ or system Also known as: Limited function or disability of body organ or system | disability of body organ or system | limited function of body organ or system | Limited function or disability of blood or blood forming organs | Limited function of blood or blood forming organs Excludes: Difficulty or need for assistance with activities [6B60.Z] Dissociative neurological symptom disorder, with unspecified symptoms Also known as: Dissociative neurological symptom disorder, with unspecified symptoms | Dissociative neurological symptom disorder | Functional neurological disorders | Functional neurological symptom disorder | Conversion disorder [8D43.Z] Neurological disorders due to toxicity, unspecified Also known as: Neurological disorders due to toxicity, unspecified | Neurological disorders due to toxicity [8D43.Y] Other specified neurological disorders due to toxicity Also known as: Other specified neurological disorders due to toxicity | Certain specified neurological disorders due to toxicity | Neurological disorder due to insect bite | Neurological disorder due to reptile bite | Encephalomyelopathy due to toxicity [MD93] Dysphagia Definition: Difficulty in swallowing which may result from neuromuscular disorder or mechanical obstruction. Dysphagia is classified into two distinct types: oropharyngeal dysphagia due to malfunction of the pharynx and upper oesophageal sphincter; and oesophageal dysphagia due to malfunction of the oesophagus. Also known as: Dysphagia | Difficulty in swallowing | difficulty swallowing | difficulty in swallowing NOS | swallowing problem Includes: Difficulty in swallowing Excludes: Functional swallowing disorder [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 === GRAPH WALKS === --- Walk 1 --- [QF10] Limited function or disability of body organ or system --PARENT--> [?] Factors influencing health status --CHILD--> [?] Problems associated with the environment --- Walk 2 --- [QF10] Limited function or disability of body organ or system --EXCLUDES--> [?] Difficulty or need for assistance with activities Def: Identifies activities for which the person needs assistance or has such difficulty with, that it affects their need for health services or their treatment.... --EXCLUDES--> [?] Dependence on enabling machines or devices --- Walk 3 --- [6B60.Z] Dissociative neurological symptom disorder, with unspecified symptoms --PARENT--> [6B60] Dissociative neurological symptom disorder Def: Dissociative neurological symptom disorder is characterised by the presentation of motor, sensory, or cognitive symptoms that imply an involuntary discontinuity in the normal integration of motor, sen... --EXCLUDES--> [?] Factitious disorders Def: Factitious disorders are characterised by intentionally feigning, falsifying, inducing, or aggravating medical, psychological, or behavioural signs and symptoms or injury in oneself or in another pers... --- Walk 4 --- [6B60.Z] Dissociative neurological symptom disorder, with unspecified symptoms --PARENT--> [6B60] Dissociative neurological symptom disorder Def: Dissociative neurological symptom disorder is characterised by the presentation of motor, sensory, or cognitive symptoms that imply an involuntary discontinuity in the normal integration of motor, sen... --EXCLUDES--> [?] Factitious disorders Def: Factitious disorders are characterised by intentionally feigning, falsifying, inducing, or aggravating medical, psychological, or behavioural signs and symptoms or injury in oneself or in another pers... --- Walk 5 --- [8D43.Z] Neurological disorders due to toxicity, unspecified --PARENT--> [8D43] Neurological disorders due to toxicity --PARENT--> [?] Nutritional or toxic disorders of the nervous system --- Walk 6 --- [8D43.Z] Neurological disorders due to toxicity, unspecified --PARENT--> [8D43] Neurological disorders due to toxicity --CHILD--> [8D43.1] Cognitive impairment due to toxicity Def: These are conditions of impaired cognition due to the toxicity of substances....
[ "[QF10] Limited function or disability of body organ or system\n --PARENT--> [?] Factors influencing health status\n --CHILD--> [?] Problems associated with the environment", "[QF10] Limited function or disability of body organ or system\n --EXCLUDES--> [?] Difficulty or need for assistance with activities\n Def: Identifies activities for which the person needs assistance or has such difficulty with, that it affects their need for health services or their treatment....\n --EXCLUDES--> [?] Dependence on enabling machines or devices", "[6B60.Z] Dissociative neurological symptom disorder, with unspecified symptoms\n --PARENT--> [6B60] Dissociative neurological symptom disorder\n Def: Dissociative neurological symptom disorder is characterised by the presentation of motor, sensory, or cognitive symptoms that imply an involuntary discontinuity in the normal integration of motor, sen...\n --EXCLUDES--> [?] Factitious disorders\n Def: Factitious disorders are characterised by intentionally feigning, falsifying, inducing, or aggravating medical, psychological, or behavioural signs and symptoms or injury in oneself or in another pers...", "[6B60.Z] Dissociative neurological symptom disorder, with unspecified symptoms\n --PARENT--> [6B60] Dissociative neurological symptom disorder\n Def: Dissociative neurological symptom disorder is characterised by the presentation of motor, sensory, or cognitive symptoms that imply an involuntary discontinuity in the normal integration of motor, sen...\n --EXCLUDES--> [?] Factitious disorders\n Def: Factitious disorders are characterised by intentionally feigning, falsifying, inducing, or aggravating medical, psychological, or behavioural signs and symptoms or injury in oneself or in another pers...", "[8D43.Z] Neurological disorders due to toxicity, unspecified\n --PARENT--> [8D43] Neurological disorders due to toxicity\n --PARENT--> [?] Nutritional or toxic disorders of the nervous system", "[8D43.Z] Neurological disorders due to toxicity, unspecified\n --PARENT--> [8D43] Neurological disorders due to toxicity\n --CHILD--> [8D43.1] Cognitive impairment due to toxicity\n Def: These are conditions of impaired cognition due to the toxicity of substances...." ]
QF10
Limited function or disability of body organ or system
[ { "from_icd11": "QF10", "icd10_code": "Z736", "icd10_title": "Limitation of activities due to disability" }, { "from_icd11": "6B60.Z", "icd10_code": "F449", "icd10_title": "Dissociative and conversion disorder, unspecified" }, { "from_icd11": "6B60.Z", "icd10_code": "F442", "icd10_title": "Dissociative stupor" }, { "from_icd11": "6B60.Z", "icd10_code": "F44", "icd10_title": "Dissociative and conversion disorders" }, { "from_icd11": "8D43.Z", "icd10_code": "T6591XA", "icd10_title": "Toxic effect of unspecified substance, accidental (unintentional), initial encounter" }, { "from_icd11": "8D43.Z", "icd10_code": "T6591XS", "icd10_title": "Toxic effect of unspecified substance, accidental (unintentional), sequela" }, { "from_icd11": "8D43.Z", "icd10_code": "T6594XA", "icd10_title": "Toxic effect of unspecified substance, undetermined, initial encounter" }, { "from_icd11": "8D43.Z", "icd10_code": "T6592XA", "icd10_title": "Toxic effect of unspecified substance, intentional self-harm, initial encounter" }, { "from_icd11": "8D43.Z", "icd10_code": "T6593XA", "icd10_title": "Toxic effect of unspecified substance, assault, initial encounter" }, { "from_icd11": "8D43.Z", "icd10_code": "T6592XS", "icd10_title": "Toxic effect of unspecified substance, intentional self-harm, sequela" }, { "from_icd11": "8D43.Z", "icd10_code": "T6593XS", "icd10_title": "Toxic effect of unspecified substance, assault, sequela" }, { "from_icd11": "8D43.Z", "icd10_code": "T6594XS", "icd10_title": "Toxic effect of unspecified substance, undetermined, sequela" }, { "from_icd11": "8D43.Z", "icd10_code": "T6591", "icd10_title": "Toxic effect of unspecified substance, accidental (unintentional)" }, { "from_icd11": "8D43.Z", "icd10_code": "T659", "icd10_title": "Toxic effect of unspecified substance" }, { "from_icd11": "MD93", "icd10_code": "R1312", "icd10_title": "Dysphagia, oropharyngeal phase" } ]
Z736
Limitation of activities due to disability
Macroscopically, the lesion was a well-circumscribed, solid white tumor and measured 18 × 15 × 10 mm in size . Histologically, hematoxylin and eosin staining revealed that the tumor was composed of atypical spindle cells with eosinophilic cytoplasm derived from proper mucous membrane and submucosa . Immunohistochemistry demonstrated that the tumor cells were positive for alpha-smooth muscle antin and desmin , but negative for CD34 and S-100 protein, which was consistent with preoperative biopsy specimens. Ki-67 index was estimated to be 60% . Based on these findings, the diagnosis of leiomyosarcoma was confirmed. Post-operative course was uneventful and the patient was discharged on postoperative day 9. The patient underwent computed tomography scans every 6 months and EGD annually for postoperative surveillance. The patient also had blood work done every 3 months. The patient is currently in good condition without recurrence or metastasis at 12 months after surgery. Fig. 3 Pathological findings. Hematoxylin and eosin staining shows well-developed fascicles of atypical spindle cells with eosinophilic cytoplasm ( a ) (200×); derived from proper mucous membrane and submucosa ( b ) (100×). Immunohistochemistry showed the tumor cells were positive for alpha-smooth muscle actin ( c ) (200×), and desmin ( d ) (200×), and negative for CD 34 ( e ) (100×). Ki-67 index was estimated to be 60% ( f ) (100×)
4.035156
0.94873
sec[1]/p[3]
en
0.999995
34143361
https://doi.org/10.1186/s40792-021-01218-3
[ "tumor", "cells", "well", "hematoxylin", "eosin", "staining", "that", "atypical", "spindle", "eosinophilic" ]
[ { "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": "MF9Y", "title": "Other specified clinical findings on examination of urine, without diagnosis" }, { "code": "5C56.20", "title": "Mucolipidosis" }, { "code": "3A51.1", "title": "Sickle cell disease without crisis" }, { "code": "9A96.3", "title": "Primary anterior uveitis" }, { "code": "3A61.Z", "title": "Acquired pure red cell aplasia, unspecified" } ]
=== 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 [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) [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] [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 === 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 --RELATED_TO--> [?] Pathological fracture in neoplastic disease of unknown behaviour --- 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--> [?] Enlarged lymph nodes Def: Enlarged lymph node is called lymphadenopathy which means the abnormal enlargement of lymph nodes.... --EXCLUDES--> [?] Nonspecific mesenteric lymphadenitis --- 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 --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 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
[ "[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", "[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--> [?] Enlarged lymph nodes\n Def: Enlarged lymph node is called lymphadenopathy which means the abnormal enlargement of lymph nodes....\n --EXCLUDES--> [?] Nonspecific mesenteric lymphadenitis", "[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 --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....", "[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" ]
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
The procedure for patient 5 was performed in the operating room with intraoperative MRI. The patient was positioned on the AtamA® board, which was mounted on the operating table and allows for frameless stereotaxy. The head was immobilized in the head-fixation ring on the AtamA® board and remained fixed throughout the procedure. We employed frameless stereotaxy to place the Mini Bolt along a preplanned trajectory using the BrainLab VarioGuide mounted on the AtamA® board. No intraoperative CT was necessary. After covering the Mini Bolt with a sterile cap, the sterile drapes were removed and the bolt was covered with sterile gauze. The patient was transported to the intraoperative MRI (3T MAGNETOM Skyra, Siemens), where under sterile conditions we placed the RPD and the NeuroBlate probe through the Mini Bolt. Subsequent T1 MPRAGE sequence with half-dose of gadolinium confirmed accurate placement of the probe within the tumor target. Ablation was monitored with MR thermography. After completion of the ablation, we obtained an additional T1 MPRAGE sequence with half-dose gadolinium. The probe and RPD were then removed, and the Mini Bolt was capped under sterile conditions. The patient was returned to the operating table, while still on the AtamA® board. There, the Mini Bolt was removed, and the incision was closed with 3-0 Nylon suture. We then removed the patient’s head from the head-fixation ring.
3.859375
0.925781
sec[1]/p[11]
en
0.999997
33489596
https://doi.org/10.7759/cureus.12186
[ "bolt", "mini", "sterile", "atama", "board", "head", "operating", "intraoperative", "probe", "mounted" ]
[ { "code": "8C72.0Y", "title": "Other specified congenital myopathy with structural abnormalities" }, { "code": "PA04&XE9EE&XE6PF", "title": "Unintentional land transport traffic event injuring an occupant of a minibus" }, { "code": "GA31.Z", "title": "Female infertility without specification whether primary or secondary" }, { "code": "GB04.Z", "title": "Male infertility, unspecified" }, { "code": "1D01.Z", "title": "Infectious meningitis, unspecified" }, { "code": "PL11.4", "title": "Failure of sterile precautions, as mode of injury or harm" }, { "code": "5A81.1", "title": "Testicular hypofunction" }, { "code": "PA92&XE9TW", "title": "Striking against diving board" }, { "code": "PA4Z", "title": "Unintentional water transport injury event with damage to water vessel unspecified" }, { "code": "PA50.Z&XE1JR&XE9Y1", "title": "Person injured while boarding or alighting from aircraft" } ]
=== ICD-11 CODES FOUND === [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 [GA31.Z] Female infertility without specification whether primary or secondary Also known as: Female infertility without specification whether primary or secondary | Female infertility | female infertility of unspecified origin | female sterility NOS | inability to achieve a pregnancy [GB04.Z] Male infertility, unspecified Also known as: Male infertility, unspecified | Male infertility | male sterility | absolute infertility [1D01.Z] Infectious meningitis, unspecified Also known as: Infectious meningitis, unspecified | Infectious meningitis, not elsewhere classified | acute meningomyelitis | septic meningitis NOS | infectious meningitis NEC [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 [5A81.1] Testicular hypofunction Definition: 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 function, loss of sex drive and sterility, muscle weakness and osteoporosis (due to loss of the androgen anabolic effect). Also known as: Testicular hypofunction | hypofunction testicle | gonadal insufficiency of testis | Testicular hypogonadism NOS | undeveloped testis [PA4Z] Unintentional water transport injury event with damage to water vessel unspecified Also known as: Unintentional water transport injury event with damage to water vessel unspecified | Water transport accidents | Boat transport accident NOS | ship transport accident NOS | Watercraft transport accident NOS === GRAPH WALKS === --- Walk 1 --- [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 2 --- [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 3 --- [GA31.Z] Female infertility without specification whether primary or secondary --PARENT--> [GA31] Female infertility Def: Disease of the reproductive system defined by the failure to achieve a clinical pregnancy after 12 months or more of regular unprotected sexual intercourse.... --CHILD--> [GA31.1] Secondary female infertility Def: Infertility in a woman who has had at least one clinical pregnancy... --- Walk 4 --- [GA31.Z] Female infertility without specification whether primary or secondary --PARENT--> [GA31] Female infertility Def: Disease of the reproductive system defined by the failure to achieve a clinical pregnancy after 12 months or more of regular unprotected sexual intercourse.... --RELATED_TO--> [?] Contact with health services for fertility preservation counselling Def: A reason for encounter to counsel an individual's queries or complaints regarding fertility preservation.... --- Walk 5 --- [GB04.Z] Male infertility, unspecified --PARENT--> [GB04] Male infertility Def: Any disorder of the reproductive system affecting males, characterised by dysfunctionalities in the ejection of semen or an abnormal absence in the measurable level of sperm in semen.... --CHILD--> [GB04.0] Azoospermia Def: Any condition of the genital system affecting males, caused by obstruction of the reproductive tract, abnormal hormone levels, testicular failure, or inadequate production of spermatozoa. These condit... --- Walk 6 --- [GB04.Z] Male infertility, unspecified --PARENT--> [GB04] Male infertility Def: Any disorder of the reproductive system affecting males, characterised by dysfunctionalities in the ejection of semen or an abnormal absence in the measurable level of sperm in semen.... --PARENT--> [?] Diseases of the male genital system Def: Any disease characterised by pathological changes to the male genital system....
[ "[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...", "[GA31.Z] Female infertility without specification whether primary or secondary\n --PARENT--> [GA31] Female infertility\n Def: Disease of the reproductive system defined by the failure to achieve a clinical pregnancy after 12 months or more of regular unprotected sexual intercourse....\n --CHILD--> [GA31.1] Secondary female infertility\n Def: Infertility in a woman who has had at least one clinical pregnancy...", "[GA31.Z] Female infertility without specification whether primary or secondary\n --PARENT--> [GA31] Female infertility\n Def: Disease of the reproductive system defined by the failure to achieve a clinical pregnancy after 12 months or more of regular unprotected sexual intercourse....\n --RELATED_TO--> [?] Contact with health services for fertility preservation counselling\n Def: A reason for encounter to counsel an individual's queries or complaints regarding fertility preservation....", "[GB04.Z] Male infertility, unspecified\n --PARENT--> [GB04] Male infertility\n Def: Any disorder of the reproductive system affecting males, characterised by dysfunctionalities in the ejection of semen or an abnormal absence in the measurable level of sperm in semen....\n --CHILD--> [GB04.0] Azoospermia\n Def: Any condition of the genital system affecting males, caused by obstruction of the reproductive tract, abnormal hormone levels, testicular failure, or inadequate production of spermatozoa. These condit...", "[GB04.Z] Male infertility, unspecified\n --PARENT--> [GB04] Male infertility\n Def: Any disorder of the reproductive system affecting males, characterised by dysfunctionalities in the ejection of semen or an abnormal absence in the measurable level of sperm in semen....\n --PARENT--> [?] Diseases of the male genital system\n Def: Any disease characterised by pathological changes to the male genital system...." ]
8C72.0Y
Other specified congenital myopathy with structural abnormalities
[ { "from_icd11": "GA31.Z", "icd10_code": "N979", "icd10_title": "Female infertility, unspecified" }, { "from_icd11": "GA31.Z", "icd10_code": "N978", "icd10_title": "Female infertility of other origin" }, { "from_icd11": "GA31.Z", "icd10_code": "N970", "icd10_title": "Female infertility associated with anovulation" }, { "from_icd11": "GA31.Z", "icd10_code": "N97", "icd10_title": "Female infertility" }, { "from_icd11": "GA31.Z", "icd10_code": "N973", "icd10_title": "" }, { "from_icd11": "GA31.Z", "icd10_code": "N974", "icd10_title": "" }, { "from_icd11": "GB04.Z", "icd10_code": "N469", "icd10_title": "Male infertility, unspecified" }, { "from_icd11": "GB04.Z", "icd10_code": "N4601", "icd10_title": "Organic azoospermia" }, { "from_icd11": "GB04.Z", "icd10_code": "N46", "icd10_title": "Male infertility" }, { "from_icd11": "1D01.Z", "icd10_code": "G02", "icd10_title": "Meningitis in other infectious and parasitic diseases classified elsewhere" }, { "from_icd11": "1D01.Z", "icd10_code": "G028", "icd10_title": "" }, { "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" } ]
N979
Female infertility, unspecified
Upon transfer to our hospital, she was found to have a fever of 37.3 °C, heart rate of 90 beats/min, blood pressure of 144/83 mmHg, and oxygen saturation of 97% on room air. Physical examination revealed diffusely decreased respiratory sounds in the right lung, severe abdominal distension, and pitting edema of the lower extremities. No peripheral lymph nodes were palpable, while laboratory studies revealed mild thrombocytopenia (platelet count of 123 × 10 9 /L) and elevated levels of alkaline phosphatase (325 IU/L), soluble interleukin-2 receptor (981 U/mL), C-reactive protein (CRP) (3.0 mg/dL), and creatinine (1.71 mg/dL), along with proteinuria and microscopic hematuria ( Table 1 ). Although the patient was positive for anti-Sjögren’s-syndrome-related antigen A and anti-histidyl-tRNA synthetase antibodies, she did not fulfill the criteria for connective tissue disease. Screening tests for hepatitis B virus, hepatitis C virus, cytomegalovirus, and human immunodeficiency virus were negative. Although her serum IL-6 level was almost normal (5.0 pg/mL; reference range < 4.0 pg/mL), elevated serum VEGF levels were noted (256 pg/mL; reference range < 38.3 pg/mL). Computed tomography (CT) revealed right pleural effusion, massive ascites, and hepatosplenomegaly without enlarged lymph nodes , and bone marrow biopsy showed hypercellular marrow with megakaryocyte hyperplasia and mild reticulin fibrosis .
4.035156
0.972656
sec[1]/p[1]
en
0.999997
34577894
https://doi.org/10.3390/medicina57090971
[ "virus", "lymph", "nodes", "although", "anti", "hepatitis", "serum", "reference", "range", "marrow" ]
[ { "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": "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" } ]
=== 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 [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 === GRAPH WALKS === --- Walk 1 --- [1D9Z] Unspecified viral infection of unspecified site --PARENT--> [?] Viral infection of unspecified site --CHILD--> [1D91] Enterovirus infection of unspecified site --- Walk 2 --- [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 3 --- [1E1Z] Unspecified viral disease --PARENT--> [?] Certain other viral diseases --CHILD--> [1D80] Mumps Def: A disease caused by an infection with mumps virus. This disease commonly presents with fever, headache, fatigue, or eventually parotitis. Transmission is by contact with respiratory secretions, direct... --- Walk 4 --- [1E1Z] Unspecified viral disease --PARENT--> [?] Certain other viral diseases --RELATED_TO--> [?] Other viral diseases complicating pregnancy, childbirth or the puerperium --- Walk 5 --- [1E1Y] Other specified viral diseases --PARENT--> [?] Certain other viral diseases --RELATED_TO--> [?] Other viral diseases complicating pregnancy, childbirth or the puerperium --- Walk 6 --- [1E1Y] Other specified viral diseases --PARENT--> [?] Certain other viral diseases --CHILD--> [1D82] Cytomegaloviral disease Def: Any condition caused by an infection with cytomegalovirus (CMV). These conditions are commonly asymptomatic. Transmission is by direct contact with infected body fluids....
[ "[1D9Z] Unspecified viral infection of unspecified site\n --PARENT--> [?] Viral infection of unspecified site\n --CHILD--> [1D91] Enterovirus infection of unspecified site", "[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....", "[1E1Z] Unspecified viral disease\n --PARENT--> [?] Certain other viral diseases\n --CHILD--> [1D80] Mumps\n Def: A disease caused by an infection with mumps virus. This disease commonly presents with fever, headache, fatigue, or eventually parotitis. Transmission is by contact with respiratory secretions, direct...", "[1E1Z] Unspecified viral disease\n --PARENT--> [?] Certain other viral diseases\n --RELATED_TO--> [?] Other viral diseases complicating pregnancy, childbirth or the puerperium", "[1E1Y] Other specified viral diseases\n --PARENT--> [?] Certain other viral diseases\n --RELATED_TO--> [?] Other viral diseases complicating pregnancy, childbirth or the puerperium", "[1E1Y] Other specified viral diseases\n --PARENT--> [?] Certain other viral diseases\n --CHILD--> [1D82] Cytomegaloviral disease\n Def: Any condition caused by an infection with cytomegalovirus (CMV). These conditions are commonly asymptomatic. Transmission is by direct contact with infected body fluids...." ]
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
Nitrous oxide (N 2 O) is inhalational anesthetic agent widely used in dentistry and minor medical procedures . Nitrous oxide exerts rapid-onset anxiolytic and hallucinogenic effects, typically beginning within 10 s of inhalation and dissipating within minutes . The recreational use of nitrous oxide has surged in recent years. N 2 O can increase the risk of vitamin B 12 deficiency as it irreversibly binds and inactivates vitamin B 12 . Its chronic or heavy abuse can lead to complications such as peripheral neuropathy, subacute combined degeneration, bone marrow suppression, and even cerebral venous thrombosis (CVT) . Hyperhomocysteinemia, a consequence of vitamin B12 deficiency, is a recognized risk factor for thrombosis, which overlaps mechanistically with the hypercoagulable state observed in anti-phospholipid syndrome (APS). Although APS is an autoimmune disorder characterized by thrombotic events and persistent antiphospholipid antibodies, environmental or drug-related triggers may unmask latent disease in predisposed individuals . Pulmonary embolism with nitrous oxide inhalant abuse case with a single positive Lupus Anticoagulant (LA) test has been reported once , but it was not confirmed and the patient was COVID-19 positive. To the best of our knowledge, this is the first reported case of nitrous oxide abuse unmasking APS in a patient diagnosed with CVT and pulmonary thromboembolism (PTE).
4.261719
0.846191
sec[0]/p[0]
en
0.999998
PMC12105173
https://doi.org/10.1186/s12883-025-04237-x
[ "nitrous", "oxide", "vitamin", "abuse", "within", "risk", "deficiency", "thrombosis", "pulmonary", "inhalational" ]
[ { "code": "PB21&XM73B5", "title": "Unintentional exposure to or harmful effects of nitrous oxide" }, { "code": "PC91&XM73B5", "title": "Intentional self-harm by exposure to or harmful effects of nitrous oxide" }, { "code": "NE60", "title": "Harmful effects of drugs, medicaments or biological substances, not elsewhere classified" }, { "code": "8A45.1", "title": "White matter disorders due to toxicity" }, { "code": "PE81&XM73B5", "title": "Assault by exposure to or harmful effects of nitrous oxide" }, { "code": "CA60.8", "title": "Siderosis" }, { "code": "5C52.0Z", "title": "Inborn errors of fatty acid oxidation or ketone body metabolism, unspecified" }, { "code": "5C53.23", "title": "Mitochondrial protein translation defects" }, { "code": "5C53.2Z", "title": "Disorders of mitochondrial oxidative phosphorylation, unspecified" }, { "code": "4B01.03", "title": "Disorders of neutrophil oxidative metabolism" } ]
=== 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 [8A45.1] White matter disorders due to toxicity Also known as: White matter disorders due to toxicity | White matter disorder due to hexachlorophene toxicity | White matter disorder due to trimethyltin toxicity | White matter disorder due to carbon monoxide toxicity | White matter disorder due to heroin vapour toxicity [CA60.8] Siderosis Definition: Siderosis refers to pneumoconiosis resulting from inhalation of iron from welding fumes or from iron or hematite mine dust. Also known as: Siderosis | arc-welders' disease | arc-welders' lung | arc-welders' nodulation | arc-welders' pneumoconiosis [5C52.0Z] Inborn errors of fatty acid oxidation or ketone body metabolism, unspecified Also known as: Inborn errors of fatty acid oxidation or ketone body metabolism, unspecified | Inborn errors of fatty acid oxidation or ketone body metabolism | Fatty acid oxidation or ketogenesis disorders | disorder of fat oxidation | disorder of fatty acid metabolism [5C53.23] Mitochondrial protein translation defects Definition: This refers to defects 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 translation defects | Combined oxidative phosphorylation deficiency | Combined mitochondrial respiratory chain complex deficiency | Respiratory chain multiple deficiencies | COXPD - [Combined oxidative phosphorylation deficiency] [5C53.2Z] Disorders of mitochondrial oxidative phosphorylation, unspecified Also known as: Disorders of mitochondrial oxidative phosphorylation, unspecified | Disorders of mitochondrial oxidative phosphorylation | Mitochondrial respiratory chain disorders | OXPHOS - [oxidative phosphorylation] diseases [4B01.03] Disorders of neutrophil oxidative metabolism Also known as: Disorders of neutrophil oxidative metabolism === 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,... --CHILD--> [?] Moderate alcohol intoxication Def: Moderate alcohol intoxication is a clinically significant transient condition that develops during or shortly after the administration of alcohol that is characterised by clearly perceptible and recog... --- 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 --- [8A45.1] White matter disorders due to toxicity --RELATED_TO--> [?] Myelopathy due to radiation injury Def: Radiation myelopathy is a serious potential complication associated with radiation therapy to the spinal cord. Its exact cause is unknown. It represents a spectrum of syndromes, the most common of whi... --CHILD--> [?] Myelopathy due to delayed radiation Def: Chronic progressive radiation myelitis, typically presents several months after the conclusion of radiation. Latency periods range from 1 month to 13 years, with the shorter intervals usually seen at ... --- Walk 4 --- [8A45.1] White matter disorders due to toxicity --RELATED_TO--> [?] Myelopathy due to radiation injury Def: Radiation myelopathy is a serious potential complication associated with radiation therapy to the spinal cord. Its exact cause is unknown. It represents a spectrum of syndromes, the most common of whi... --CHILD--> [?] Myelopathy due to delayed radiation Def: Chronic progressive radiation myelitis, typically presents several months after the conclusion of radiation. Latency periods range from 1 month to 13 years, with the shorter intervals usually seen at ...
[ "[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 --CHILD--> [?] Moderate alcohol intoxication\n Def: Moderate alcohol intoxication is a clinically significant transient condition that develops during or shortly after the administration of alcohol that is characterised by clearly perceptible and recog...", "[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...", "[8A45.1] White matter disorders due to toxicity\n --RELATED_TO--> [?] Myelopathy due to radiation injury\n Def: Radiation myelopathy is a serious potential complication associated with radiation therapy to the spinal cord. Its exact cause is unknown. It represents a spectrum of syndromes, the most common of whi...\n --CHILD--> [?] Myelopathy due to delayed radiation\n Def: Chronic progressive radiation myelitis, typically presents several months after the conclusion of radiation. Latency periods range from 1 month to 13 years, with the shorter intervals usually seen at ...", "[8A45.1] White matter disorders due to toxicity\n --RELATED_TO--> [?] Myelopathy due to radiation injury\n Def: Radiation myelopathy is a serious potential complication associated with radiation therapy to the spinal cord. Its exact cause is unknown. It represents a spectrum of syndromes, the most common of whi...\n --CHILD--> [?] Myelopathy due to delayed radiation\n Def: Chronic progressive radiation myelitis, typically presents several months after the conclusion of radiation. Latency periods range from 1 month to 13 years, with the shorter intervals usually seen at ..." ]
PB21&XM73B5
Unintentional exposure to or harmful effects of nitrous oxide
[ { "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
Metastatic mucinous tumors can be very similar to the primary ovarian mucinous tumors, grossly. Our case showed the right ovary having multiple mucin-filled cystic areas along with many areas of necrosis. The solid areas were also mostly necrosed with evidence of hemorrhage. Grossly, the gallbladder did not show any mass, but its wall was diffusely thickened. Occasionally, these tumors pose major diagnostic problems microscopically, particularly when there is a bland-appearing epithelium or an adenofibroma or cystadenoma-like pattern. The presence of these bland and borderline-like areas could mislead one into concluding that the carcinoma arose out of a background primary ovarian neoplasm. Not infrequently, well-differentiated glands and cysts dispersed in prominent fibrous stroma strikingly mimicked ovarian adenofibroma, and similar well-differentiated cysts in a less conspicuous stroma mimicked a cystadenoma. 2 Similar misinterpretation of such an area as a pre-existing ovarian lesion could lead one to wrongly conclude that the entire process was primary in the ovary. Awareness of this phenomenon and attention to the clinical findings, gross features, and other histologic indicators of metastatic disease, as noted previously, should enable one to avoid this diagnostic pitfall. However, in a limited sample, such as the intraoperative frozen section, this can be a particularly treacherous area.
4.203125
0.541992
sec[2]/p[2]
en
0.999996
34307215
https://doi.org/10.4322/acr.2021.248
[ "ovarian", "areas", "tumors", "similar", "this", "metastatic", "mucinous", "grossly", "ovary", "these" ]
[ { "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" }, { "code": "QF29", "title": "Difficulty or need for assistance with major areas of life" }, { "code": "EH40.1Y", "title": "Other specified infantile napkin dermatoses" }, { "code": "GA90", "title": "Hyperplasia of prostate" }, { "code": "2B66.Z", "title": "Malignant neoplasms of other or unspecified parts of mouth, unspecified" }, { "code": "EG63.Z", "title": "Sacrococcygeal pilonidal disease, unspecified" } ]
=== ICD-11 CODES FOUND === [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 [QF29] Difficulty or need for assistance with major areas of life Also known as: Difficulty or need for assistance with major areas of life | difficulty with major areas of life | need for assistance with major areas of life | Difficulty or need for assistance with education | Difficulty or needs for assistance with work and economic life [EH40.1Y] Other specified infantile napkin dermatoses Also known as: Other specified infantile napkin dermatoses | Infections of the napkin area [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 [2B66.Z] Malignant neoplasms of other or unspecified parts of mouth, unspecified Also known as: Malignant neoplasms of other or unspecified parts of mouth, unspecified | Malignant neoplasms of other or unspecified parts of mouth | cancer of buccal mucosa | cancer of cheek mucosa | internal cheek cancer [EG63.Z] Sacrococcygeal pilonidal disease, unspecified Also known as: Sacrococcygeal pilonidal disease, unspecified | Sacrococcygeal pilonidal disease | pilonidal disease of sacrococcygeal area | sacrococcygeal pilonidal disease NOS === GRAPH WALKS === --- Walk 1 --- [GA30.6] Premature ovarian failure Def: 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 conce... --RELATED_TO--> [?] Secondary amenorrhoea Def: In women who have menstruated previously, no menses for an interval of time equivalent to a total of at least 3 previous cycles, or 6 months... --CHILD--> [?] Premature ovarian failure due to autoimmune oophoritis Def: This refers to the loss of function of the ovaries before age 40, due to autoimmune inflammation of the ovaries.... --- Walk 2 --- [GA30.6] Premature ovarian failure Def: 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 conce... --EXCLUDES--> [?] 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... --CHILD--> [?] Acquired hypopituitarism Def: This is the acquired decreased (hypo) secretion of one or more of the eight hormones normally produced by the pituitary gland at the base of the brain.... --- Walk 3 --- [JA01.2] Ovarian pregnancy Def: A condition characterised by implantation of the embryo within the ovary during pregnancy.... --PARENT--> [JA01] Ectopic pregnancy Def: Any condition characterised by implantation of the embryo outside the endometrium and endometrial cavity during pregnancy.... --CHILD--> [JA01.0] Abdominal pregnancy Def: A condition characterised by implantation of the embryo within the peritoneal cavity during pregnancy.... --- Walk 4 --- [JA01.2] Ovarian pregnancy Def: A condition characterised by implantation of the embryo within the ovary during pregnancy.... --PARENT--> [JA01] Ectopic pregnancy Def: Any condition characterised by implantation of the embryo outside the endometrium and endometrial cavity during pregnancy.... --CHILD--> [JA01.0] Abdominal pregnancy Def: A condition characterised by implantation of the embryo within the peritoneal cavity during pregnancy.... --- Walk 5 --- [QF01.10] Acquired absence of female genital organs --RELATED_TO--> [?] 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... --PARENT--> [?] Acquired absence of female genital organs --- Walk 6 --- [QF01.10] Acquired absence of female genital organs --RELATED_TO--> [?] 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... --PARENT--> [?] Other conditions of the genitourinary system Def: Any disorder characterised by pathological changes to the genitourinary system....
[ "[GA30.6] Premature ovarian failure\n Def: 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 conce...\n --RELATED_TO--> [?] Secondary amenorrhoea\n Def: In women who have menstruated previously, no menses for an interval of time equivalent to a total of at least 3 previous cycles, or 6 months...\n --CHILD--> [?] Premature ovarian failure due to autoimmune oophoritis\n Def: This refers to the loss of function of the ovaries before age 40, due to autoimmune inflammation of the ovaries....", "[GA30.6] Premature ovarian failure\n Def: 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 conce...\n --EXCLUDES--> [?] 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 --CHILD--> [?] Acquired hypopituitarism\n Def: This is the acquired decreased (hypo) secretion of one or more of the eight hormones normally produced by the pituitary gland at the base of the brain....", "[JA01.2] Ovarian pregnancy\n Def: A condition characterised by implantation of the embryo within the ovary 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--> [JA01.0] Abdominal pregnancy\n Def: A condition characterised by implantation of the embryo within the peritoneal cavity during pregnancy....", "[JA01.2] Ovarian pregnancy\n Def: A condition characterised by implantation of the embryo within the ovary 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--> [JA01.0] Abdominal pregnancy\n Def: A condition characterised by implantation of the embryo within the peritoneal cavity during pregnancy....", "[QF01.10] Acquired absence of female genital organs\n --RELATED_TO--> [?] 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...\n --PARENT--> [?] Acquired absence of female genital organs", "[QF01.10] Acquired absence of female genital organs\n --RELATED_TO--> [?] 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...\n --PARENT--> [?] Other conditions of the genitourinary system\n Def: Any disorder characterised by pathological changes to the genitourinary system...." ]
GA1Z&XA1QK0
Noninflammatory disorders of ovary
[ { "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" }, { "from_icd11": "QF29", "icd10_code": "Z742", "icd10_title": "Need for assistance at home and no other household member able to render care" }, { "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": "2B66.Z", "icd10_code": "C0689", "icd10_title": "Malignant neoplasm of overlapping sites of other parts of mouth" }, { "from_icd11": "2B66.Z", "icd10_code": "C062", "icd10_title": "Malignant neoplasm of retromolar area" }, { "from_icd11": "2B66.Z", "icd10_code": "C060", "icd10_title": "Malignant neoplasm of cheek mucosa" } ]
E2839
Other primary ovarian failure
In February 2021, the patient underwent AZD1222 COVID-19 vaccination (first dose injected into her left arm). Four days later, another PET/CT was performed to exclude new extracerebral metastases (PET2). No sign of melanoma recurrence was found in the iliac lymph nodes or central nervous system. However, a metabolically active lymph node in the left axillary region was noted . The lymph node had the dimension of 9 × 7 mm, and the maximal standardized uptake value was 5.2. Additionally, an area of increased 18 F-FDG accumulation was found in the left deltoid muscle that corresponded to the site of the recent vaccination. An inflammatory reaction to the injection was suspected to be responsible for the 18 F-FDG accumulation in the axillary lymph node. However, in order to rule out a melanoma metastasis in the axillary lymph node, a follow-up PET/CT (PET3) was recommended 28 days later . This scan did not present any 18 F-FDG accumulation in the reported lymph node. The diameter of the node did not change. No other finding was reported, except for a focus of slightly increased 18 F-FDG accumulation (diameter of 10 mm) in the right cerebellar lobe that had not been present in the PET2 scan. Fortunately, the subsequent MRI did not confirm any lesion in the cerebellum and did not show any other intracranial recurrence. However, further MRI monitoring of the central nervous system has been recommended.
4.015625
0.964355
sec[1]/p[2]
en
0.999999
34414110
https://doi.org/10.3389/fonc.2021.690443
[ "lymph", "node", "accumulation", "however", "axillary", "vaccination", "melanoma", "recurrence", "nervous", "system" ]
[ { "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": "FA20.0", "title": "Seropositive rheumatoid arthritis" }, { "code": "MF30", "title": "Breast lump or mass female" }, { "code": "BB40", "title": "Acute or subacute infectious endocarditis" }, { "code": "FA0Z", "title": "Osteoarthritis, unspecified" }, { "code": "FA85.10", "title": "Localised central endplate defect" } ]
=== 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 [FA20.0] Seropositive rheumatoid arthritis Also known as: Seropositive rheumatoid arthritis | high positive rheumatoid factor | low positive rheumatoid factor | high positive anticitrullinated protein antibody | low positive anticitrullinated protein antibody [MF30] Breast lump or mass female Also known as: Breast lump or mass female | breast irregular nodularity | breast node | lump in breast | lump or mass in breast NOS [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 [FA0Z] Osteoarthritis, unspecified Also known as: Osteoarthritis, unspecified | osteoarthritis NOS | arthrosis NOS | OA - [osteoarthritis] | Osteoarthritis with determinants [FA85.10] Localised central endplate defect Also known as: Localised central endplate defect | Schmorl nodes | schmorl's nodes | schmorl's nodules === 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.... --CHILD--> [BD92] Lymphangiectasia --- 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.... --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 3 --- [BD90.Z] Lymphadenitis, unspecified --PARENT--> [BD90] Lymphadenitis --CHILD--> [BD90.0] Acute 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 --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...
[ "[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 --CHILD--> [BD92] Lymphangiectasia", "[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...", "[BD90.Z] Lymphadenitis, unspecified\n --PARENT--> [BD90] Lymphadenitis\n --CHILD--> [BD90.0] Acute 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 --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..." ]
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": "FA20.0", "icd10_code": "M0569", "icd10_title": "Rheumatoid arthritis of multiple sites with involvement of other organs and systems" }, { "from_icd11": "FA20.0", "icd10_code": "M0579", "icd10_title": "Rheumatoid arthritis with rheumatoid factor of multiple sites without organ or systems involvement" }, { "from_icd11": "FA20.0", "icd10_code": "M05612", "icd10_title": "Rheumatoid arthritis of left shoulder with involvement of other organs and systems" }, { "from_icd11": "FA20.0", "icd10_code": "M0570", "icd10_title": "Rheumatoid arthritis with rheumatoid factor of unspecified site without organ or systems involvement" }, { "from_icd11": "FA20.0", "icd10_code": "M0560", "icd10_title": "Rheumatoid arthritis of unspecified site with involvement of other organs and systems" }, { "from_icd11": "FA20.0", "icd10_code": "M0500", "icd10_title": "Felty's syndrome, unspecified site" } ]
I898
Other specified noninfective disorders of lymphatic vessels and lymph nodes
A 12-month-old male was referred because of fever, seizure and anemia while suffering from fever and diarrhea for 3 days. The seizure was upward gaze with generalized tonic–clonic movement in a few seconds. In the initial examination, abdominal distention and hepatosplenomegaly were observed. At admission, laboratory findings showed leukocytosis with lymphocytosis and decreased hemoglobin. The main findings of LP were pleocytosis with 90% lymph and negative for bacterial growth. The molecular test for SARS-CoV-2 and HSV-1 and 2 in CSF was negative. With suspicion of meningoencephalitis, wide-spectrum antibiotics were used. CT scan showed peripherally located patchy consolidations and ground-glass opacities in the basal segments of the right-lower lobe and inferior aspects of the right-middle lobe and lingula . SARS-CoV-2 and TB tests in respiratory samples were negative. Because of the reverse in CD4/CD8 ratio, an HIV test was ordered and reported as negative. The molecular test for SARS-CoV-2 again was negative. Abdominal sonography and CT scan showed hepatosplenomegaly and lymphadenopathy in the para -aorta and celiac trunk. Although his brain CT scan and MRI findings were normal, bone marrow aspiration revealed mild erythroid hyperplasia. Nasopharyngeal swab became positive for SARS-CoV-2 on day 18. Treatment was started with hydroxychloroquine, and the patient became well and was discharged.
3.859375
0.985352
sec[0]/sec[1]/p[0]
en
0.999997
34650617
https://doi.org/10.2217/fvl-2021-0091
[ "sars", "scan", "because", "fever", "seizure", "abdominal", "hepatosplenomegaly", "molecular", "lobe", "became" ]
[ { "code": "1D65", "title": "Severe acute respiratory syndrome" }, { "code": "RA01.0", "title": "COVID-19, virus identified" }, { "code": "RA01.0/CA40.1Z", "title": "COVID-19 with pneumonia, SARS-CoV-2 identified" }, { "code": "RA01.1/CA40.1Z", "title": "COVID-19 with pneumonia, SARS-CoV-2 not identified" }, { "code": "MB71.Y", "title": "Other specified clinical findings on diagnostic imaging of central nervous system" }, { "code": "NE60", "title": "Harmful effects of drugs, medicaments or biological substances, not elsewhere classified" }, { "code": "JA66.3", "title": "Abnormal ultrasonic finding on antenatal screening of mother" }, { "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" }, { "code": "QC10", "title": "Procedure not carried out because of contraindication" } ]
=== ICD-11 CODES FOUND === [1D65] Severe acute respiratory syndrome Definition: A disease of the respiratory system, caused by an infection with coronavirus. This disease is characterised by fever, headache, cough, myalgia, tachycardia, or diarrhoea. This disease may also lead to pneumonia. Transmission is by direct contact, inhalation of infected respiratory secretions, or airborne transmission. Confirmation is by identification of coronavirus in a blood, stool, respiratory secretions, or body tissue sample. Also known as: Severe acute respiratory syndrome | SARS - [severe acute respiratory syndrome] Excludes: COVID-19, virus identified | COVID-19, virus not identified [RA01.0] COVID-19, virus identified Also known as: COVID-19, virus identified | 2019-new Coronavirus acute respiratory disease (deprecated) | 2019-nCoV acute respiratory disease [temporary name] (deprecated) | Coronavirus disease 2019 | SARS-CoV-2 disease Includes: Coronavirus disease 2019 | COVID-19 NOS Excludes: Coronavirus infection, unspecified site | Middle East respiratory syndrome | Severe acute respiratory syndrome [MB71.Y] Other specified clinical findings on diagnostic imaging of central nervous system Also known as: Other specified clinical findings on diagnostic imaging of central nervous system | Epidural haemorrhage, localised, no generalised mass effect or midline shift | Epidural haemorrhage, confined to a small region in relation to a fracture | Epidural haemorrhage, size less than 1 x 1 x 1 cm, not in relation to a fracture | Epidural haemorrhage, mass effect or midline shift less than 0.5 cm [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 [JA66.3] Abnormal ultrasonic finding on antenatal screening of mother Definition: A sign characterised by an abnormality detected by ultrasound during an antenatal screening of the mother. Also known as: Abnormal ultrasonic finding on antenatal screening of mother | antenatal ultrasound scan abnormal [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 [QC10] Procedure not carried out because of contraindication Also known as: Procedure not carried out because of contraindication | intervention not carried out because of contraindication | Procedure cancelled due to contraindication === GRAPH WALKS === --- Walk 1 --- [1D65] Severe acute respiratory syndrome Def: A disease of the respiratory system, caused by an infection with coronavirus. This disease is characterised by fever, headache, cough, myalgia, tachycardia, or diarrhoea. This disease may also lead to... --EXCLUDES--> [?] COVID-19, virus not identified --CHILD--> [?] COVID-19 with pneumonia, SARS-CoV-2 not identified --- Walk 2 --- [1D65] Severe acute respiratory syndrome Def: A disease of the respiratory system, caused by an infection with coronavirus. This disease is characterised by fever, headache, cough, myalgia, tachycardia, or diarrhoea. This disease may also lead to... --EXCLUDES--> [?] COVID-19, virus identified --EXCLUDES--> [?] Severe acute respiratory syndrome Def: A disease of the respiratory system, caused by an infection with coronavirus. This disease is characterised by fever, headache, cough, myalgia, tachycardia, or diarrhoea. This disease may also lead to... --- Walk 3 --- [RA01.0] COVID-19, virus identified --EXCLUDES--> [?] Middle East respiratory syndrome Def: A disease caused by an infection with Middle East Respiratory Syndrome coronavirus (MERS-CoA). This disease is characterised by severe acute respiratory illness with fever, cough, and shortness of bre... --PARENT--> [?] Certain zoonotic viral diseases --- Walk 4 --- [RA01.0] COVID-19, virus identified --EXCLUDES--> [?] Coronavirus infection, unspecified site --EXCLUDES--> [?] Severe acute respiratory syndrome Def: A disease of the respiratory system, caused by an infection with coronavirus. This disease is characterised by fever, headache, cough, myalgia, tachycardia, or diarrhoea. This disease may also lead to... --- Walk 5 --- [MB71.Y] Other specified clinical findings on diagnostic imaging of central nervous system --PARENT--> [MB71] Clinical findings on diagnostic imaging of central nervous system Def: Clinical findings on diagnostic imaging of central nervous system is findings on diagnostic imaging of the brain or the spinal cord which don't appear in normal status of the body. Diagnostic imaging ... --CHILD--> [MB71.0] Intracranial space-occupying lesion --- Walk 6 --- [MB71.Y] Other specified clinical findings on diagnostic imaging of central nervous system --PARENT--> [MB71] Clinical findings on diagnostic imaging of central nervous system Def: Clinical findings on diagnostic imaging of central nervous system is findings on diagnostic imaging of the brain or the spinal cord which don't appear in normal status of the body. Diagnostic imaging ... --PARENT--> [?] Clinical findings in the nervous system
[ "[1D65] Severe acute respiratory syndrome\n Def: A disease of the respiratory system, caused by an infection with coronavirus. This disease is characterised by fever, headache, cough, myalgia, tachycardia, or diarrhoea. This disease may also lead to...\n --EXCLUDES--> [?] COVID-19, virus not identified\n --CHILD--> [?] COVID-19 with pneumonia, SARS-CoV-2 not identified", "[1D65] Severe acute respiratory syndrome\n Def: A disease of the respiratory system, caused by an infection with coronavirus. This disease is characterised by fever, headache, cough, myalgia, tachycardia, or diarrhoea. This disease may also lead to...\n --EXCLUDES--> [?] COVID-19, virus identified\n --EXCLUDES--> [?] Severe acute respiratory syndrome\n Def: A disease of the respiratory system, caused by an infection with coronavirus. This disease is characterised by fever, headache, cough, myalgia, tachycardia, or diarrhoea. This disease may also lead to...", "[RA01.0] COVID-19, virus identified\n --EXCLUDES--> [?] Middle East respiratory syndrome\n Def: A disease caused by an infection with Middle East Respiratory Syndrome coronavirus (MERS-CoA). This disease is characterised by severe acute respiratory illness with fever, cough, and shortness of bre...\n --PARENT--> [?] Certain zoonotic viral diseases", "[RA01.0] COVID-19, virus identified\n --EXCLUDES--> [?] Coronavirus infection, unspecified site\n --EXCLUDES--> [?] Severe acute respiratory syndrome\n Def: A disease of the respiratory system, caused by an infection with coronavirus. This disease is characterised by fever, headache, cough, myalgia, tachycardia, or diarrhoea. This disease may also lead to...", "[MB71.Y] Other specified clinical findings on diagnostic imaging of central nervous system\n --PARENT--> [MB71] Clinical findings on diagnostic imaging of central nervous system\n Def: Clinical findings on diagnostic imaging of central nervous system is findings on diagnostic imaging of the brain or the spinal cord which don't appear in normal status of the body. Diagnostic imaging ...\n --CHILD--> [MB71.0] Intracranial space-occupying lesion", "[MB71.Y] Other specified clinical findings on diagnostic imaging of central nervous system\n --PARENT--> [MB71] Clinical findings on diagnostic imaging of central nervous system\n Def: Clinical findings on diagnostic imaging of central nervous system is findings on diagnostic imaging of the brain or the spinal cord which don't appear in normal status of the body. Diagnostic imaging ...\n --PARENT--> [?] Clinical findings in the nervous system" ]
1D65
Severe acute respiratory syndrome
[ { "from_icd11": "1D65", "icd10_code": "U04", "icd10_title": "" }, { "from_icd11": "1D65", "icd10_code": "U049", "icd10_title": "" }, { "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": "" } ]
U04
However, the patient complained of pain in his upper abdomen followed by nausea and vomiting on the 5th day, when he was supposed to be discharged. The abdominal computed tomography revealed an unusually elevated left hemi-diaphragm with displacement of colon to left upper quadrant . This was not evident on a chest x-ray (CXR) taken 4 months previously. Ultrasound of chest detected a thin diaphragm with nearly no diaphragmatic movement in the left side during deep breathing (Supplemental Video (Video that demonstrates the normal right diaphragmatic excursion and contraction during deep inspiration, but no diaphragmatic movement in the left side, 1 minute, 33MB), http://links.lww.com/MD/F569 ). Inspiratory/expiratory CXRs revealed little movement of the left diaphragm , raising suspicion of DP secondary to phrenic nerve palsy. Furthermore, the brachial plexus magnetic resonance imaging showed left C5 and C6 root avulsion injuries . A diagnosis of brachial plexus injury, occurring concurrently with left hemidiaphragmatic paralysis caused by phrenic nerve palsy was made. The subsequent pulmonary function test (PFT) showed significant ventilatory impairment, forced vital capacity (FVC) 2.28L (61% of predicated value), and forced expiratory volume in 1s 65L (53% of predicated value) with a mild diffusion defect. The patient had no shortness of breath and was discharged on day 7 with oral mecobalamin.
3.966797
0.977539
sec[1]/p[1]
en
0.999997
33530199
https://doi.org/10.1097/MD.0000000000024043
[ "diaphragm", "diaphragmatic", "movement", "discharged", "chest", "side", "video", "expiratory", "phrenic", "nerve" ]
[ { "code": "CB23", "title": "Disorders of diaphragm" }, { "code": "LB00.1", "title": "Absence of diaphragm" }, { "code": "NB32.Y&XA2JL0", "title": "Laceration of diaphragm" }, { "code": "LB00.Y", "title": "Other specified structural developmental anomalies of diaphragm" }, { "code": "DC51.1&XA2JL0", "title": "Adhesion of diaphragm" }, { "code": "LB00.Z", "title": "Structural developmental anomalies of diaphragm, unspecified" }, { "code": "DD50.0", "title": "Diaphragmatic hernia" }, { "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" } ]
=== ICD-11 CODES FOUND === [CB23] Disorders of diaphragm Definition: This category includes the abnormalities of diaphragmatic position or motion (paralysis, relaxation, and acquired deformity) and the inflammation of the diaphragm, but neoplasms of the diaphragm, congenital malformation of diaphragm, and diaphragmatic hernias are included in other categories. Also known as: Disorders of diaphragm | diaphragmatic disorder | disease of diaphragm | disorder of diaphragm | Acquired diaphragmatic deformity Excludes: Congenital diaphragmatic hernia | Structural developmental anomalies of diaphragm [LB00.1] Absence of diaphragm Also known as: Absence of diaphragm | diaphragm agenesis [LB00.Y] Other specified structural developmental anomalies of diaphragm Also known as: Other specified structural developmental anomalies of diaphragm | Eventration of diaphragm | diaphragm elevation | high diaphragm | Oesophageal hiatus hypertrophy [LB00.Z] Structural developmental anomalies of diaphragm, unspecified Also known as: Structural developmental anomalies of diaphragm, unspecified | Structural developmental anomalies of diaphragm | congenital diaphragm deformity | diaphragmatic anomaly | CDD - [congenital diaphragmatic defect] [DD50.0] Diaphragmatic hernia Definition: A hernia occurs through the foramen in the diaphragm. Also known as: Diaphragmatic hernia | hiatus hernia | oesophageal hiatus hernia | paraoesophageal hernia | sliding hiatus hernia Includes: paraoesophageal hernia Excludes: Congenital diaphragmatic hernia | Congenital hiatus hernia [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 === GRAPH WALKS === --- Walk 1 --- [CB23] Disorders of diaphragm Def: This category includes the abnormalities of diaphragmatic position or motion (paralysis, relaxation, and acquired deformity) and the inflammation of the diaphragm, but neoplasms of the diaphragm, cong... --EXCLUDES--> [?] Structural developmental anomalies of diaphragm --CHILD--> [?] Absence of diaphragm --- Walk 2 --- [CB23] Disorders of diaphragm Def: This category includes the abnormalities of diaphragmatic position or motion (paralysis, relaxation, and acquired deformity) and the inflammation of the diaphragm, but neoplasms of the diaphragm, cong... --EXCLUDES--> [?] Structural developmental anomalies of diaphragm --PARENT--> [?] Structural developmental anomalies of the diaphragm, abdominal wall or umbilical cord Def: Any condition caused by failure of the diaphragm, abdominal wall or umbilical cord to correctly develop during the antenatal period.... --- Walk 3 --- [LB00.1] Absence of diaphragm --PARENT--> [LB00] Structural developmental anomalies of diaphragm --PARENT--> [?] Structural developmental anomalies of the diaphragm, abdominal wall or umbilical cord Def: Any condition caused by failure of the diaphragm, abdominal wall or umbilical cord to correctly develop during the antenatal period.... --- Walk 4 --- [LB00.1] Absence of diaphragm --PARENT--> [LB00] Structural developmental anomalies of diaphragm --CHILD--> [LB00.Y] Other specified structural developmental anomalies of diaphragm --- Walk 5 --- [LB00.Y] Other specified structural developmental anomalies of diaphragm --PARENT--> [LB00] Structural developmental anomalies of diaphragm --CHILD--> [LB00.Y] Other specified structural developmental anomalies of diaphragm --- Walk 6 --- [LB00.Y] Other specified structural developmental anomalies of diaphragm --PARENT--> [LB00] Structural developmental anomalies of diaphragm --CHILD--> [LB00.0] Congenital diaphragmatic hernia Def: Congenital diaphragmatic hernia is a posterolateral defect of the diaphragm that allows passage of abdominal viscera into the thorax, leading to respiratory insufficiency and persistent pulmonary hype...
[ "[CB23] Disorders of diaphragm\n Def: This category includes the abnormalities of diaphragmatic position or motion (paralysis, relaxation, and acquired deformity) and the inflammation of the diaphragm, but neoplasms of the diaphragm, cong...\n --EXCLUDES--> [?] Structural developmental anomalies of diaphragm\n --CHILD--> [?] Absence of diaphragm", "[CB23] Disorders of diaphragm\n Def: This category includes the abnormalities of diaphragmatic position or motion (paralysis, relaxation, and acquired deformity) and the inflammation of the diaphragm, but neoplasms of the diaphragm, cong...\n --EXCLUDES--> [?] Structural developmental anomalies of diaphragm\n --PARENT--> [?] Structural developmental anomalies of the diaphragm, abdominal wall or umbilical cord\n Def: Any condition caused by failure of the diaphragm, abdominal wall or umbilical cord to correctly develop during the antenatal period....", "[LB00.1] Absence of diaphragm\n --PARENT--> [LB00] Structural developmental anomalies of diaphragm\n --PARENT--> [?] Structural developmental anomalies of the diaphragm, abdominal wall or umbilical cord\n Def: Any condition caused by failure of the diaphragm, abdominal wall or umbilical cord to correctly develop during the antenatal period....", "[LB00.1] Absence of diaphragm\n --PARENT--> [LB00] Structural developmental anomalies of diaphragm\n --CHILD--> [LB00.Y] Other specified structural developmental anomalies of diaphragm", "[LB00.Y] Other specified structural developmental anomalies of diaphragm\n --PARENT--> [LB00] Structural developmental anomalies of diaphragm\n --CHILD--> [LB00.Y] Other specified structural developmental anomalies of diaphragm", "[LB00.Y] Other specified structural developmental anomalies of diaphragm\n --PARENT--> [LB00] Structural developmental anomalies of diaphragm\n --CHILD--> [LB00.0] Congenital diaphragmatic hernia\n Def: Congenital diaphragmatic hernia is a posterolateral defect of the diaphragm that allows passage of abdominal viscera into the thorax, leading to respiratory insufficiency and persistent pulmonary hype..." ]
CB23
Disorders of diaphragm
[ { "from_icd11": "CB23", "icd10_code": "J986", "icd10_title": "Disorders of diaphragm" }, { "from_icd11": "LB00.1", "icd10_code": "Q791", "icd10_title": "Other congenital malformations of diaphragm" }, { "from_icd11": "LB00.Z", "icd10_code": "Q799", "icd10_title": "Congenital malformation of musculoskeletal system, unspecified" }, { "from_icd11": "DD50.0", "icd10_code": "K449", "icd10_title": "Diaphragmatic hernia without obstruction or gangrene" }, { "from_icd11": "DD50.0", "icd10_code": "K440", "icd10_title": "Diaphragmatic hernia with obstruction, without gangrene" }, { "from_icd11": "DD50.0", "icd10_code": "K441", "icd10_title": "Diaphragmatic hernia with gangrene" }, { "from_icd11": "DD50.0", "icd10_code": "K44", "icd10_title": "Diaphragmatic hernia" }, { "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" } ]
J986
Disorders of diaphragm
She is a 66-year-old woman with a history of endometrial cancer and chemoradiotherapy following hysterectomy. She sustained a pelvic fracture 11 months afterwards with initially suspected disease recurrence on MRI prompting eventual PET/CT and multiple biopsies which were negative. She continued to have pain and gait issues for another year and developed a right thigh abscess confirmed by CT. Additionally, a possible fistulous communication with the bladder and left pelvis was noted; however, this was not further evaluated or definitively managed beyond abscess drainage at that time. Repeat CT 1 month later was notable for pubosymphyseal diastasis with fragmented pubic bone fractures. Approximately 2 years later, she developed sepsis due to a right groin abscess which was drained by general surgery; however, this re-accumulated 1 week later prompting percutaneous drainage. Upon noting high drain output with low urinary output, an elevated drain creatinine level was determined and raised concern for a urinary fistula. CT cystogram subsequently confirmed the fistula and her care was transferred to our institution after receiving bilateral nephrostomy tube and urethral catheter diversions. Three months later, she underwent surgical extirpation with rectus muscle interposition flap. Post-operatively, she developed an ileus requiring 3-day nasogastric decompression. She was discharged on ceftriaxone.
3.583984
0.986328
sec[1]/sec[0]/sec[3]/p[0]
en
0.999996
34386191
https://doi.org/10.1093/jscr/rjab331
[ "abscess", "prompting", "which", "however", "this", "drainage", "drain", "output", "urinary", "fistula" ]
[ { "code": "1B75.3", "title": "Pyogenic abscess of the skin" }, { "code": "FB30", "title": "Infectious myositis" }, { "code": "FA10.Z", "title": "Direct infections of joint, unspecified" }, { "code": "FB84.Y", "title": "Other specified osteomyelitis or osteitis" }, { "code": "FB40.0", "title": "Infectious tenosynovitis" }, { "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": "4A01.03", "title": "Transient hypogammaglobulinaemia of infancy" } ]
=== ICD-11 CODES FOUND === [1B75.3] Pyogenic abscess of the skin Definition: A pus-producing abscess of the skin most commonly due to bacterial infection by Staphylococcus aureus. It is prone to develop where the normal anatomy is disturbed as in pilonidal disease, an epidermoid cyst or around foreign bodies such as surgical sutures. Also known as: Pyogenic abscess of the skin | abscess NOS [FB30] Infectious myositis Definition: Infective myositis is an acute, subacute, or chronic infection of skeletal muscle and may be caused by a wide range of infecting organisms. Immunosuppression, particularly as the result of HIV infection, is an important predisposing factor. Also known as: Infectious myositis | Bacterial myositis | Bacterial pyomyositis | Tropical muscle abscess | Tropical pyomyositis [FA10.Z] Direct infections of joint, unspecified Also known as: Direct infections of joint, unspecified | Direct infections of joint | septic arthritis | pyogenic arthritis | arthritis due to infection [FB84.Y] Other specified osteomyelitis or osteitis Also known as: Other specified osteomyelitis or osteitis | Other chronic osteomyelitis | Garre's disease | chronic or old osteomyelitis with or without mention of periostitis | chronic bone abscess [FB40.0] Infectious tenosynovitis Also known as: Infectious tenosynovitis | Bacterial infection of tendon sheath | Fungal infection of tendon sheath | Mycobacterial infection of tendon sheath | Parasitic infection of tendon sheath [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 [4A01.03] Transient hypogammaglobulinaemia of infancy Also known as: Transient hypogammaglobulinaemia of infancy | immunoglobulin maturational delay | THI - [transient hypogammaglobulinaemia of infancy] === GRAPH WALKS === --- Walk 1 --- [1B75.3] Pyogenic abscess of the skin Def: A pus-producing abscess of the skin most commonly due to bacterial infection by Staphylococcus aureus. It is prone to develop where the normal anatomy is disturbed as in pilonidal disease, an epidermo... --RELATED_TO--> [?] Infected epidermoid cyst Def: An epidermoid cyst which has become secondarily infected by, most commonly, Staphylococcus aureus. It manifests as pain, swelling and erythema of a preexisting cyst and is predisposed to rupture.... --PARENT--> [?] Pyogenic abscess of the skin Def: A pus-producing abscess of the skin most commonly due to bacterial infection by Staphylococcus aureus. It is prone to develop where the normal anatomy is disturbed as in pilonidal disease, an epidermo... --- Walk 2 --- [1B75.3] Pyogenic abscess of the skin Def: A pus-producing abscess of the skin most commonly due to bacterial infection by Staphylococcus aureus. It is prone to develop where the normal anatomy is disturbed as in pilonidal disease, an epidermo... --RELATED_TO--> [?] Infected epidermoid cyst Def: An epidermoid cyst which has become secondarily infected by, most commonly, Staphylococcus aureus. It manifests as pain, swelling and erythema of a preexisting cyst and is predisposed to rupture.... --PARENT--> [?] Pyogenic abscess of the skin Def: A pus-producing abscess of the skin most commonly due to bacterial infection by Staphylococcus aureus. It is prone to develop where the normal anatomy is disturbed as in pilonidal disease, an epidermo... --- Walk 3 --- [FB30] Infectious myositis Def: Infective myositis is an acute, subacute, or chronic infection of skeletal muscle and may be caused by a wide range of infecting organisms. Immunosuppression, particularly as the result of HIV infecti... --PARENT--> [?] Disorders of muscles --PARENT--> [?] Soft tissue disorders --- Walk 4 --- [FB30] Infectious myositis Def: Infective myositis is an acute, subacute, or chronic infection of skeletal muscle and may be caused by a wide range of infecting organisms. Immunosuppression, particularly as the result of HIV infecti... --PARENT--> [?] Disorders of muscles --EXCLUDES--> [?] Muscular dystrophy Def: Progressive, hereditary skeletal muscle diseases characterised by muscle weakness, wasting, defects in muscle proteins, necrosis of muscle tissue and replacement of muscle tissue with connective and f... --- Walk 5 --- [FA10.Z] Direct infections of joint, unspecified --PARENT--> [FA10] Direct infections of joint Def: Hematogenic or non-hematogenic infections of joints.... --CHILD--> [FA10.2] Fungal infection of joint --- Walk 6 --- [FA10.Z] Direct infections of joint, unspecified --PARENT--> [FA10] Direct infections of joint Def: Hematogenic or non-hematogenic infections of joints.... --EXCLUDES--> [?] Reactive arthropathies Def: A disease of the joints, caused by an infection in another part of the body, auto-immune disease, or post-vaccination. This disease is characterised by a secondary inflammation of the joints in reacti...
[ "[1B75.3] Pyogenic abscess of the skin\n Def: A pus-producing abscess of the skin most commonly due to bacterial infection by Staphylococcus aureus. It is prone to develop where the normal anatomy is disturbed as in pilonidal disease, an epidermo...\n --RELATED_TO--> [?] Infected epidermoid cyst\n Def: An epidermoid cyst which has become secondarily infected by, most commonly, Staphylococcus aureus. It manifests as pain, swelling and erythema of a preexisting cyst and is predisposed to rupture....\n --PARENT--> [?] Pyogenic abscess of the skin\n Def: A pus-producing abscess of the skin most commonly due to bacterial infection by Staphylococcus aureus. It is prone to develop where the normal anatomy is disturbed as in pilonidal disease, an epidermo...", "[1B75.3] Pyogenic abscess of the skin\n Def: A pus-producing abscess of the skin most commonly due to bacterial infection by Staphylococcus aureus. It is prone to develop where the normal anatomy is disturbed as in pilonidal disease, an epidermo...\n --RELATED_TO--> [?] Infected epidermoid cyst\n Def: An epidermoid cyst which has become secondarily infected by, most commonly, Staphylococcus aureus. It manifests as pain, swelling and erythema of a preexisting cyst and is predisposed to rupture....\n --PARENT--> [?] Pyogenic abscess of the skin\n Def: A pus-producing abscess of the skin most commonly due to bacterial infection by Staphylococcus aureus. It is prone to develop where the normal anatomy is disturbed as in pilonidal disease, an epidermo...", "[FB30] Infectious myositis\n Def: Infective myositis is an acute, subacute, or chronic infection of skeletal muscle and may be caused by a wide range of infecting organisms. Immunosuppression, particularly as the result of HIV infecti...\n --PARENT--> [?] Disorders of muscles\n --PARENT--> [?] Soft tissue disorders", "[FB30] Infectious myositis\n Def: Infective myositis is an acute, subacute, or chronic infection of skeletal muscle and may be caused by a wide range of infecting organisms. Immunosuppression, particularly as the result of HIV infecti...\n --PARENT--> [?] Disorders of muscles\n --EXCLUDES--> [?] Muscular dystrophy\n Def: Progressive, hereditary skeletal muscle diseases characterised by muscle weakness, wasting, defects in muscle proteins, necrosis of muscle tissue and replacement of muscle tissue with connective and f...", "[FA10.Z] Direct infections of joint, unspecified\n --PARENT--> [FA10] Direct infections of joint\n Def: Hematogenic or non-hematogenic infections of joints....\n --CHILD--> [FA10.2] Fungal infection of joint", "[FA10.Z] Direct infections of joint, unspecified\n --PARENT--> [FA10] Direct infections of joint\n Def: Hematogenic or non-hematogenic infections of joints....\n --EXCLUDES--> [?] Reactive arthropathies\n Def: A disease of the joints, caused by an infection in another part of the body, auto-immune disease, or post-vaccination. This disease is characterised by a secondary inflammation of the joints in reacti..." ]
1B75.3
Pyogenic abscess of the skin
[ { "from_icd11": "1B75.3", "icd10_code": "L02612", "icd10_title": "Cutaneous abscess of left foot" }, { "from_icd11": "1B75.3", "icd10_code": "L02611", "icd10_title": "Cutaneous abscess of right foot" }, { "from_icd11": "1B75.3", "icd10_code": "L02511", "icd10_title": "Cutaneous abscess of right hand" }, { "from_icd11": "1B75.3", "icd10_code": "L02512", "icd10_title": "Cutaneous abscess of left hand" }, { "from_icd11": "1B75.3", "icd10_code": "L02619", "icd10_title": "Cutaneous abscess of unspecified foot" }, { "from_icd11": "1B75.3", "icd10_code": "L02519", "icd10_title": "Cutaneous abscess of unspecified hand" }, { "from_icd11": "1B75.3", "icd10_code": "L02529", "icd10_title": "Furuncle unspecified hand" }, { "from_icd11": "1B75.3", "icd10_code": "L02539", "icd10_title": "Carbuncle of unspecified hand" }, { "from_icd11": "1B75.3", "icd10_code": "L02629", "icd10_title": "Furuncle of unspecified foot" }, { "from_icd11": "1B75.3", "icd10_code": "L02639", "icd10_title": "Carbuncle of unspecified foot" }, { "from_icd11": "1B75.3", "icd10_code": "L02214", "icd10_title": "Cutaneous abscess of groin" }, { "from_icd11": "1B75.3", "icd10_code": "L02414", "icd10_title": "Cutaneous abscess of left upper limb" }, { "from_icd11": "1B75.3", "icd10_code": "L0231", "icd10_title": "Cutaneous abscess of buttock" }, { "from_icd11": "1B75.3", "icd10_code": "L02413", "icd10_title": "Cutaneous abscess of right upper limb" }, { "from_icd11": "1B75.3", "icd10_code": "L02212", "icd10_title": "Cutaneous abscess of back [any part, except buttock]" } ]
L02612
Cutaneous abscess of left foot
The following case is of a 10-year-old boy with a regressive form of ASD, where milestones and speech had been lost. At the time of presentation, he exhibited significant developmental and language delays, problems with socialization, no eye contact, and anxiety and panic to the level where he could not sleep alone. He was also obsessed with electronic games. His speech was characterized by talking in the third person and problems with receptive language. He had difficulties explaining what he wanted, generally communicating with pointing. He would have flares of PANDAS (pediatric autoimmune neuropsychiatric disorders associated with streptococcal infection) where OCD-like behaviors, including tics, aggression, biting, and evidence of paranoid thoughts would be exhibited. Many of these symptoms were resolved when antibiotics for strep were given. He had been treated with five courses of antibiotics in the six months before presentation to the clinician. He had also presented on a gluten-free, dairy-free diet and had been on that for six years. The only ASD “specific” treatments he had been given were some “herbal tinctures” for immune support. Before addressing genomics, as per their usual protocol, TACGA worked on his gut microbiome inflammation and addressed his diet and nutrient deficiencies. Similar to the experiences of other clinicians, some improvements were seen with these interventions.
3.822266
0.984863
sec[4]/sec[1]/sec[0]/p[0]
en
0.999996
PMC8879068
https://doi.org/10.3390/ijms23042167
[ "speech", "language", "problems", "these", "antibiotics", "free", "diet", "regressive", "form", "milestones" ]
[ { "code": "MA80.Z", "title": "Speech or language disturbances, unspecified" }, { "code": "MB23.L", "title": "Pressured speech" }, { "code": "6B60.5", "title": "Dissociative neurological symptom disorder, with speech disturbance" }, { "code": "MB25.02", "title": "Disorganised thinking" }, { "code": "MA81", "title": "Speech dysfluency" }, { "code": "6A01.2", "title": "Developmental language disorder" }, { "code": "6A01.Z", "title": "Developmental speech or language disorders, unspecified" }, { "code": "6A01.20", "title": "Developmental language disorder with impairment of receptive and expressive language" }, { "code": "6A01.21", "title": "Developmental language disorder with impairment of mainly expressive language" }, { "code": "QE70.Z", "title": "Problems related to primary support group, including family circumstances, unspecified" } ]
=== ICD-11 CODES FOUND === [MA80.Z] Speech or language disturbances, unspecified Also known as: Speech or language disturbances, unspecified | Speech or language disturbances | speech defect NOS | speech disorder NOS | problem with voice production [MB23.L] Pressured speech Definition: Speech in which the person feels undue pressure to get the words out. The person’s speech is usually rapid, loud, and emphatic and may be difficult or impossible to interrupt. Frequently, the person talks without any social stimulation and may continue to talk even though no one is listening. Also known as: Pressured speech Excludes: Schizophrenia or other primary psychotic disorders | Bipolar or related disorders [6B60.5] Dissociative neurological symptom disorder, with speech disturbance Definition: Dissociative neurological symptom disorder, with speech disturbance is characterised by symptoms such as difficulty with speaking (dysphonia), loss of the ability to speak (aphonia) or difficult or unclear articulation of speech (dysarthria) that are not consistent with a recognised disease of the nervous system, a neurodevelopmental or neurocognitive disorder, other mental, behavioural or neurodevelopmental disorder, or other medical condition and do not occur exclusively during another dissoci Also known as: Dissociative neurological symptom disorder, with speech disturbance | Functional neurological symptom disorder, with speech disturbance | Functional speech disorder [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 [MA81] Speech dysfluency Definition: 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 limits of normal variation and results in reduced intelligibility and significantly affects communication. It can involve repetitions of sounds, syllables or words, prolongations, word breaks, blockage of production, excessive use of interjections, and rapid short bursts of speech. Also known as: Speech dysfluency | speech impediment NOS | Adult onset cluttering | Adult onset stammering | Adult onset stuttering Excludes: Developmental language disorder | Developmental speech or language disorders | Developmental speech fluency disorder [6A01.2] Developmental language disorder Definition: Developmental language disorder is characterised by persistent deficits in the acquisition, understanding, production or use of language (spoken or signed), that arise during the developmental period, typically during early childhood, and cause significant limitations in the individual’s ability to communicate. The individual’s ability to understand, produce or use language is markedly below what would be expected given the individual’s age. The language deficits are not explained by another neu Also known as: Developmental language disorder | language development disorder | language learning impairment | specific language impairment Excludes: Autism spectrum disorder | Diseases of the nervous system | Deafness not otherwise specified [6A01.Z] Developmental speech or language disorders, unspecified Also known as: Developmental speech or language disorders, unspecified | Developmental speech or language disorders | developmental language impairment | developmental speech and language disorder | developmental speech or language disorder [6A01.20] Developmental language disorder with impairment of receptive and expressive language Definition: Developmental language disorder with impairment of receptive and expressive language is characterised by persistent difficulties in the acquisition, understanding, production, and use of language that arise during the developmental period, typically during early childhood, and cause significant limitations in the individual’s ability to communicate. The ability to understand spoken or signed language (i.e., receptive language) is markedly below the expected level given the individual’s age and l Also known as: Developmental language disorder with impairment of receptive and expressive language | developmental receptive language disorder | receptive language disorder | developmental dysphasia or aphasia, receptive type | mixed receptive language disorder Includes: developmental dysphasia or aphasia, receptive type Excludes: acquired aphasia with epilepsy [Landau-Kleffner] | Autism spectrum disorder | Selective mutism [6A01.21] Developmental language disorder with impairment of mainly expressive language Definition: Developmental language disorder with impairment of mainly expressive language is characterised by persistent difficulties in the acquisition, production, and use of language that arise during the developmental period, typically during early childhood, and cause significant limitations in the individual’s ability to communicate. The ability to produce and use spoken or signed language (i.e., expressive language) is markedly below the expected level given the individual’s age and level of intellec Also known as: Developmental language disorder with impairment of mainly expressive language | developmental expressive language disorder | Developmental dysphasia or aphasia, expressive type | Developmental expressive dysphasia | Developmental expressive type aphasia Includes: Developmental dysphasia or aphasia, expressive type Excludes: acquired aphasia with epilepsy [Landau-Kleffner] | Selective mutism | dysphasia and aphasia: developmental, receptive type [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 === GRAPH WALKS === --- Walk 1 --- [MA80.Z] Speech or language disturbances, unspecified --PARENT--> [MA80] Speech or language disturbances Def: Speech or language disturbances, not classified elsewhere include dysphasia and aphasia, dysarthria and anarthria, and other speech or language disturbances.... --CHILD--> [MA80.1] Dysphasia Def: A cognitive disorder marked by an impaired ability to comprehend or express language in its written or spoken form. This condition is caused by diseases which affect the language areas of the dominant... --- Walk 2 --- [MA80.Z] Speech or language disturbances, unspecified --PARENT--> [MA80] Speech or language disturbances Def: Speech or language disturbances, not classified elsewhere include dysphasia and aphasia, dysarthria and anarthria, and other speech or language disturbances.... --PARENT--> [?] Symptoms or signs involving speech, language or voice --- Walk 3 --- [MB23.L] Pressured speech Def: Speech in which the person feels undue pressure to get the words out. The person’s speech is usually rapid, loud, and emphatic and may be difficult or impossible to interrupt. Frequently, the person t... --EXCLUDES--> [?] Bipolar or related disorders Def: Bipolar and related disorders are episodic mood disorders defined by the occurrence of Manic, Mixed or Hypomanic episodes or symptoms. These episodes typically alternate over the course of these disor... --CHILD--> [?] Bipolar type I disorder Def: Bipolar type I disorder is an episodic mood disorder defined by the occurrence of one or more manic or mixed episodes. A manic episode is an extreme mood state lasting at least one week unless shorten... --- Walk 4 --- [MB23.L] Pressured speech Def: Speech in which the person feels undue pressure to get the words out. The person’s speech is usually rapid, loud, and emphatic and may be difficult or impossible to interrupt. Frequently, the person t... --EXCLUDES--> [?] Schizophrenia or other primary psychotic disorders Def: Schizophrenia and other primary psychotic disorders are characterised by significant impairments in reality testing and alterations in behaviour manifest in positive symptoms such as persistent delusi... --CHILD--> [?] Schizotypal disorder Def: Schizotypal disorder is characterised by an enduring pattern (i.e. characteristic of the person’s functioning over a period of at least several years) of eccentricities in behaviour, appearance and sp... --- Walk 5 --- [6B60.5] Dissociative neurological symptom disorder, with speech disturbance Def: Dissociative neurological symptom disorder, with speech disturbance is characterised by symptoms such as difficulty with speaking (dysphonia), loss of the ability to speak (aphonia) or difficult or un... --PARENT--> [6B60] Dissociative neurological symptom disorder Def: Dissociative neurological symptom disorder is characterised by the presentation of motor, sensory, or cognitive symptoms that imply an involuntary discontinuity in the normal integration of motor, sen... --CHILD--> [6B60.1] Dissociative neurological symptom disorder, with auditory disturbance Def: 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... --- Walk 6 --- [6B60.5] Dissociative neurological symptom disorder, with speech disturbance Def: Dissociative neurological symptom disorder, with speech disturbance is characterised by symptoms such as difficulty with speaking (dysphonia), loss of the ability to speak (aphonia) or difficult or un... --PARENT--> [6B60] Dissociative neurological symptom disorder Def: Dissociative neurological symptom disorder is characterised by the presentation of motor, sensory, or cognitive symptoms that imply an involuntary discontinuity in the normal integration of motor, sen... --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...
[ "[MA80.Z] Speech or language disturbances, unspecified\n --PARENT--> [MA80] Speech or language disturbances\n Def: Speech or language disturbances, not classified elsewhere include dysphasia and aphasia, dysarthria and anarthria, and other speech or language disturbances....\n --CHILD--> [MA80.1] Dysphasia\n Def: A cognitive disorder marked by an impaired ability to comprehend or express language in its written or spoken form. This condition is caused by diseases which affect the language areas of the dominant...", "[MA80.Z] Speech or language disturbances, unspecified\n --PARENT--> [MA80] Speech or language disturbances\n Def: Speech or language disturbances, not classified elsewhere include dysphasia and aphasia, dysarthria and anarthria, and other speech or language disturbances....\n --PARENT--> [?] Symptoms or signs involving speech, language or voice", "[MB23.L] Pressured speech\n Def: Speech in which the person feels undue pressure to get the words out. The person’s speech is usually rapid, loud, and emphatic and may be difficult or impossible to interrupt. Frequently, the person t...\n --EXCLUDES--> [?] Bipolar or related disorders\n Def: Bipolar and related disorders are episodic mood disorders defined by the occurrence of Manic, Mixed or Hypomanic episodes or symptoms. These episodes typically alternate over the course of these disor...\n --CHILD--> [?] Bipolar type I disorder\n Def: Bipolar type I disorder is an episodic mood disorder defined by the occurrence of one or more manic or mixed episodes. A manic episode is an extreme mood state lasting at least one week unless shorten...", "[MB23.L] Pressured speech\n Def: Speech in which the person feels undue pressure to get the words out. The person’s speech is usually rapid, loud, and emphatic and may be difficult or impossible to interrupt. Frequently, the person t...\n --EXCLUDES--> [?] Schizophrenia or other primary psychotic disorders\n Def: Schizophrenia and other primary psychotic disorders are characterised by significant impairments in reality testing and alterations in behaviour manifest in positive symptoms such as persistent delusi...\n --CHILD--> [?] Schizotypal disorder\n Def: Schizotypal disorder is characterised by an enduring pattern (i.e. characteristic of the person’s functioning over a period of at least several years) of eccentricities in behaviour, appearance and sp...", "[6B60.5] Dissociative neurological symptom disorder, with speech disturbance\n Def: Dissociative neurological symptom disorder, with speech disturbance is characterised by symptoms such as difficulty with speaking (dysphonia), loss of the ability to speak (aphonia) or difficult or un...\n --PARENT--> [6B60] Dissociative neurological symptom disorder\n Def: Dissociative neurological symptom disorder is characterised by the presentation of motor, sensory, or cognitive symptoms that imply an involuntary discontinuity in the normal integration of motor, sen...\n --CHILD--> [6B60.1] Dissociative neurological symptom disorder, with auditory disturbance\n Def: 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...", "[6B60.5] Dissociative neurological symptom disorder, with speech disturbance\n Def: Dissociative neurological symptom disorder, with speech disturbance is characterised by symptoms such as difficulty with speaking (dysphonia), loss of the ability to speak (aphonia) or difficult or un...\n --PARENT--> [6B60] Dissociative neurological symptom disorder\n Def: Dissociative neurological symptom disorder is characterised by the presentation of motor, sensory, or cognitive symptoms that imply an involuntary discontinuity in the normal integration of motor, sen...\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..." ]
MA80.Z
Speech or language disturbances, unspecified
[ { "from_icd11": "MA80.Z", "icd10_code": "R479", "icd10_title": "Unspecified speech disturbances" }, { "from_icd11": "MA80.Z", "icd10_code": "R4702", "icd10_title": "Dysphasia" }, { "from_icd11": "MA80.Z", "icd10_code": "R4789", "icd10_title": "Other speech disturbances" }, { "from_icd11": "MA80.Z", "icd10_code": "R4781", "icd10_title": "Slurred speech" }, { "from_icd11": "MA80.Z", "icd10_code": "R4782", "icd10_title": "Fluency disorder in conditions classified elsewhere" }, { "from_icd11": "MA80.Z", "icd10_code": "R47", "icd10_title": "Speech disturbances, not elsewhere classified" }, { "from_icd11": "MA80.Z", "icd10_code": "R470", "icd10_title": "Dysphasia and aphasia" }, { "from_icd11": "MA80.Z", "icd10_code": "R478", "icd10_title": "Other speech disturbances" }, { "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": "6A01.2", "icd10_code": "F809", "icd10_title": "Developmental disorder of speech and language, unspecified" }, { "from_icd11": "6A01.Z", "icd10_code": "F8081", "icd10_title": "Childhood onset fluency disorder" }, { "from_icd11": "6A01.Z", "icd10_code": "F8089", "icd10_title": "Other developmental disorders of speech and language" }, { "from_icd11": "6A01.Z", "icd10_code": "F80", "icd10_title": "Specific developmental disorders of speech and language" } ]
R479
Unspecified speech disturbances
Despite the delayed presentation to our unit, the patient was treated in accordance with the BOAST 4 guidelines for severe open lower limb injuries. Intraoperatively, wound exploration revealed no signs of early infection, and following a discussion about the various options of treating the wound, it was closed in conjunction with the plastic surgeons. Examination under anesthesia prior to stabilization revealed gross valgus laxity and instability in external rotation. The patient then underwent stabilization of the three joint dislocations: 1. Open reduction of the patellofemoral dislocation with reconstruction of the medial patellofemoral ligament with ipsilateral semitendinosus tendon autograft. 2. Medial collateral ligament repair with suture anchors at femoral insertion 3. Medial meniscal root and body repair. 4. Reduction under anesthesia of the proximal tibiofibular joint. After reduction, the joint was stable and did not require additional fixation. 5. In view of the open nature of the injury, it was felt that the ACL and PCL partial injuries should be assessed at a later date and not treated with immediate reconstruction due to the risk of septic arthritis. The peripheral tibial plateau avulsion fracture did not require internal fixation. 6. A knee-spanning external fixator was constructed to maintain reduction of the tibiofemoral joint and enable inspection of the injured soft tissues.
3.728516
0.974121
sec[1]/sec[1]/p[0]
en
0.999996
34991682
https://doi.org/10.1186/s13256-021-03201-w
[ "joint", "reduction", "open", "treated", "injuries", "wound", "anesthesia", "stabilization", "patellofemoral", "reconstruction" ]
[ { "code": "FA5Z", "title": "Arthropathies, unspecified" }, { "code": "FA2Z", "title": "Inflammatory arthropathies, unspecified" }, { "code": "FA36.Z", "title": "Effusion of joint, unspecified" }, { "code": "FA37.Y", "title": "Other specified certain joint disorders, not elsewhere classified" }, { "code": "FA34.3", "title": "Contracture of joint" }, { "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 === [FA5Z] Arthropathies, unspecified Also known as: Arthropathies, unspecified | Disorders affecting predominantly peripheral joints | Disorders affecting predominantly peripheral limb joints | arthropathy NOS | arthropathic [FA2Z] Inflammatory arthropathies, unspecified Also known as: Inflammatory arthropathies, unspecified | polyarthritis NOS | inflammatory joint disease NOS | nonpyogenic arthritis NOS | arthritic nodosa [FA36.Z] Effusion of joint, unspecified Also known as: Effusion of joint, unspecified | Effusion of joint | effusion into joint | effusion of joint, site unspecified | hydrarthrosis [FA37.Y] Other specified certain joint disorders, not elsewhere classified Also known as: Other specified certain joint disorders, not elsewhere classified | Calcification of joint | Periarticular calcification | Periarticular ossification | Fistula of joint [FA34.3] Contracture of joint Also known as: Contracture of joint | contracture of joint, site unspecified | joint contraction | joint contracture | abduction contracture joint Excludes: Dupuytren contracture | contracture of tendon (sheath) without contracture of joint | acquired deformities of limbs [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 --- [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 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 --- [FA2Z] Inflammatory arthropathies, unspecified --PARENT--> [?] Inflammatory arthropathies --RELATED_TO--> [?] Peripheral spondyloarthritis Def: Experts from the Assessment of SpondyloArthritis international Society (ASAS) developed classification criteria for axSpA and peripheral SpA. These criteria were developed for patients with peripheral... --- Walk 4 --- [FA2Z] Inflammatory arthropathies, unspecified --PARENT--> [?] Inflammatory arthropathies --RELATED_TO--> [?] Peripheral spondyloarthritis Def: Experts from the Assessment of SpondyloArthritis international Society (ASAS) developed classification criteria for axSpA and peripheral SpA. These criteria were developed for patients with peripheral... --- Walk 5 --- [FA36.Z] Effusion of joint, unspecified --PARENT--> [FA36] Effusion of joint Def: Increased intra-articular fluid secondary to trauma and/or other acquired conditions not detailed in other codes.... --EXCLUDES--> [?] Tertiary yaws Def: Tertiary yaws develops in <10% of untreated infected individuals after and interval of 5 years or more. The late stage skin lesions are characterised by gummatous nodules with necrotic tissue destruct... --- Walk 6 --- [FA36.Z] Effusion of joint, unspecified --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
[ "[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...", "[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...", "[FA2Z] Inflammatory arthropathies, unspecified\n --PARENT--> [?] Inflammatory arthropathies\n --RELATED_TO--> [?] Peripheral spondyloarthritis\n Def: Experts from the Assessment of SpondyloArthritis international Society (ASAS) developed classification criteria for axSpA and peripheral SpA. These criteria were developed for patients with peripheral...", "[FA2Z] Inflammatory arthropathies, unspecified\n --PARENT--> [?] Inflammatory arthropathies\n --RELATED_TO--> [?] Peripheral spondyloarthritis\n Def: Experts from the Assessment of SpondyloArthritis international Society (ASAS) developed classification criteria for axSpA and peripheral SpA. These criteria were developed for patients with peripheral...", "[FA36.Z] Effusion of joint, unspecified\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 --EXCLUDES--> [?] Tertiary yaws\n Def: Tertiary yaws develops in <10% of untreated infected individuals after and interval of 5 years or more. The late stage skin lesions are characterised by gummatous nodules with necrotic tissue destruct...", "[FA36.Z] Effusion of joint, unspecified\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" ]
FA5Z
Arthropathies, unspecified
[ { "from_icd11": "FA5Z", "icd10_code": "M00-M25", "icd10_title": "" }, { "from_icd11": "FA2Z", "icd10_code": "M1389", "icd10_title": "Other specified arthritis, multiple sites" }, { "from_icd11": "FA2Z", "icd10_code": "M1380", "icd10_title": "Other specified arthritis, unspecified site" }, { "from_icd11": "FA2Z", "icd10_code": "M13862", "icd10_title": "Other specified arthritis, left knee" }, { "from_icd11": "FA2Z", "icd10_code": "M13872", "icd10_title": "Other specified arthritis, left ankle and foot" }, { "from_icd11": "FA2Z", "icd10_code": "M13871", "icd10_title": "Other specified arthritis, right ankle and foot" }, { "from_icd11": "FA2Z", "icd10_code": "M13861", "icd10_title": "Other specified arthritis, right knee" }, { "from_icd11": "FA2Z", "icd10_code": "M13879", "icd10_title": "Other specified arthritis, unspecified ankle and foot" }, { "from_icd11": "FA2Z", "icd10_code": "M13842", "icd10_title": "Other specified arthritis, left hand" }, { "from_icd11": "FA2Z", "icd10_code": "M13841", "icd10_title": "Other specified arthritis, right hand" }, { "from_icd11": "FA2Z", "icd10_code": "M13811", "icd10_title": "Other specified arthritis, right shoulder" }, { "from_icd11": "FA2Z", "icd10_code": "M13162", "icd10_title": "Monoarthritis, not elsewhere classified, left knee" }, { "from_icd11": "FA2Z", "icd10_code": "M13869", "icd10_title": "Other specified arthritis, unspecified knee" }, { "from_icd11": "FA2Z", "icd10_code": "M1388", "icd10_title": "Other specified arthritis, other site" }, { "from_icd11": "FA2Z", "icd10_code": "M13171", "icd10_title": "Monoarthritis, not elsewhere classified, right ankle and foot" } ]
M00-M25
After using the combination of BRAF + MEK inhibitors as the first line and treatment, with immune checkpoint inhibitors as a second line of treatment, i.e., the anti PD-1, treatment was limited to chemotherapy, anti CTLA-4 (ipilimumab), and radiotherapy (controversial)/re-challenge of the treatment with Dabrafenib + Trametinib (the BRAF + MEK inhibitor combination in Romania). In January 2022, the targeted treatment was reinitiated, keeping the standard doses of treatment—Dabrafenib 150 mg BID (taken two times a day), Trametinib 2 mg/day, but with extremely difficult clinical tolerance, manifested by daily chills, facial edema, including that of the lips, generalized pustular erythematous, pruriginous eruption, with areas of integumentary peeling and depigmentation—symptoms that are not controlled by corticoid and antihistaminic treatment. After a prolonged discontinuation of treatment for approximately 6 weeks, until the disappearance of the clinical complaints, the patient required admission to the Oncology Department for ongoing hospitalization for the titration of systemic treatment and clinical monitoring of the symptoms. The clinical oncological and dermatological evaluation upon the attempt to resume the treatment with Dabrafenib and Trametinib guided the diagnosis to allergic reactions to the treatment but could not rule out a cutaneous adverse reaction with severely increased potential.
4.023438
0.937988
sec[1]/p[4]
en
0.999997
PMC10178057
https://doi.org/10.3390/diagnostics13091635
[ "dabrafenib", "trametinib", "combination", "braf", "inhibitors", "line", "anti", "that", "using", "immune" ]
[ { "code": "4A01.1Z", "title": "Combined immunodeficiencies, unspecified" }, { "code": "PB29", "title": "Unintentional exposure to or harmful effects of multiple drugs, medicaments or biological substances" }, { "code": "8A40.Z", "title": "Multiple sclerosis, unspecified" }, { "code": "6C4F.3", "title": "Intoxication due to multiple specified psychoactive substances" }, { "code": "PH49", "title": "Exposure to or harmful effects of undetermined intent of multiple drugs, medicaments or biological substances" }, { "code": "3B21.Z", "title": "Haemorrhagic disorder due to unspecified circulating anticoagulants or coagulation factors" }, { "code": "HA02.0Z", "title": "Anorgasmia, unspecified" }, { "code": "6D11.3", "title": "Disinhibition in personality disorder or personality difficulty" }, { "code": "NE60", "title": "Harmful effects of drugs, medicaments or biological substances, not elsewhere classified" }, { "code": "6D86.5", "title": "Disinhibition in dementia" } ]
=== ICD-11 CODES FOUND === [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 [PB29] Unintentional exposure to or harmful effects of multiple drugs, medicaments or biological substances Also known as: Unintentional exposure to or harmful effects of multiple drugs, medicaments or biological substances | accidental overdose of multiple drugs, medicaments or biological substances | accidental poisoning by multiple drugs, medicaments or biological substances | multiple drugs, medicaments or biological substances taken in error | combined drug toxicity NOS Includes: accidental overdose of multiple drugs, medicaments or biological substances [8A40.Z] Multiple sclerosis, unspecified Also known as: Multiple sclerosis, unspecified | Multiple sclerosis | cerebrospinal sclerosis | disseminated sclerosis | generalised multiple sclerosis [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 [PH49] Exposure to or harmful effects of undetermined intent of multiple drugs, medicaments or biological substances Also known as: Exposure to or harmful effects of undetermined intent of multiple drugs, medicaments or biological substances | mixed substance toxicity NOS | acute combined drug toxicity [3B21.Z] Haemorrhagic disorder due to unspecified circulating anticoagulants or coagulation factors Also known as: Haemorrhagic disorder due to unspecified circulating anticoagulants or coagulation factors | Haemorrhagic disorder due to circulating anticoagulants or coagulation factors inhibitors | acquired coagulation factor inhibitor disorder | acquired inhibitor of coagulation | antithrombinaemia [HA02.0Z] Anorgasmia, unspecified Also known as: Anorgasmia, unspecified | Anorgasmia | abnormal orgasm | female sexual orgasmic dysfunction | male sexual orgasmic dysfunction [6D11.3] Disinhibition in personality disorder or personality difficulty Definition: The core feature of the Disinhibition trait domain is the tendency to act rashly based on immediate external or internal stimuli (i.e., sensations, emotions, thoughts), without consideration of potential negative consequences. Common manifestations of Disinhibition, not all of which may be present in a given individual at a given time, include: impulsivity; distractibility; irresponsibility; recklessness; and lack of planning. Also known as: Disinhibition in personality disorder or personality difficulty [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 [6D86.5] Disinhibition in dementia Definition: In addition to the cognitive disturbances characteristic of dementia, the current clinical picture includes clinically significant lack of restraint manifested in disregard for social conventions, impulsivity, and poor risk assessment. Also known as: Disinhibition in dementia === GRAPH WALKS === --- Walk 1 --- [4A01.1Z] Combined immunodeficiencies, unspecified --PARENT--> [4A01.1] Combined immunodeficiencies --CHILD--> [4A01.11] Major histocompatibility complex class I deficiency --- Walk 2 --- [4A01.1Z] Combined immunodeficiencies, unspecified --PARENT--> [4A01.1] Combined immunodeficiencies --CHILD--> [4A01.12] Major histocompatibility complex class II deficiency Def: Immunodeficiency by defective expression of HLA class II is an autosomal recessive primary immune deficiency, manifesting by recurrent viral and bacterial infections, often leading to chronic diarrhoe... --- Walk 3 --- [PB29] Unintentional exposure to or harmful effects of multiple drugs, medicaments or biological substances --PARENT--> [?] Unintentional exposure to or harmful effects of drugs, medicaments or biological substances --CHILD--> [PB22] Unintentional exposure to or harmful effects of psychostimulants --- Walk 4 --- [PB29] Unintentional exposure to or harmful effects of multiple drugs, medicaments or biological substances --PARENT--> [?] Unintentional exposure to or harmful effects of drugs, medicaments or biological substances --CHILD--> [PB20] Unintentional exposure to or harmful effects of opioids or related analgesics --- Walk 5 --- [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--> [8A40.2] Secondary progressive multiple sclerosis --- Walk 6 --- [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....
[ "[4A01.1Z] Combined immunodeficiencies, unspecified\n --PARENT--> [4A01.1] Combined immunodeficiencies\n --CHILD--> [4A01.11] Major histocompatibility complex class I deficiency", "[4A01.1Z] Combined immunodeficiencies, unspecified\n --PARENT--> [4A01.1] Combined immunodeficiencies\n --CHILD--> [4A01.12] Major histocompatibility complex class II deficiency\n Def: Immunodeficiency by defective expression of HLA class II is an autosomal recessive primary immune deficiency, manifesting by recurrent viral and bacterial infections, often leading to chronic diarrhoe...", "[PB29] Unintentional exposure to or harmful effects of multiple drugs, medicaments or biological substances\n --PARENT--> [?] Unintentional exposure to or harmful effects of drugs, medicaments or biological substances\n --CHILD--> [PB22] Unintentional exposure to or harmful effects of psychostimulants", "[PB29] Unintentional exposure to or harmful effects of multiple drugs, medicaments or biological substances\n --PARENT--> [?] Unintentional exposure to or harmful effects of drugs, medicaments or biological substances\n --CHILD--> [PB20] Unintentional exposure to or harmful effects of opioids or related analgesics", "[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--> [8A40.2] Secondary progressive multiple sclerosis", "[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...." ]
4A01.1Z
Combined immunodeficiencies, unspecified
[ { "from_icd11": "4A01.1Z", "icd10_code": "D8189", "icd10_title": "Other combined immunodeficiencies" }, { "from_icd11": "4A01.1Z", "icd10_code": "D819", "icd10_title": "Combined immunodeficiency, unspecified" }, { "from_icd11": "4A01.1Z", "icd10_code": "D81", "icd10_title": "Combined immunodeficiencies" }, { "from_icd11": "4A01.1Z", "icd10_code": "D815", "icd10_title": "Purine nucleoside phosphorylase [PNP] deficiency" }, { "from_icd11": "4A01.1Z", "icd10_code": "D818", "icd10_title": "Other combined immunodeficiencies" }, { "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": "3B21.Z", "icd10_code": "D6832", "icd10_title": "Hemorrhagic disorder due to extrinsic circulating anticoagulants" }, { "from_icd11": "3B21.Z", "icd10_code": "D68312", "icd10_title": "Antiphospholipid antibody with hemorrhagic disorder" }, { "from_icd11": "3B21.Z", "icd10_code": "D68318", "icd10_title": "Other hemorrhagic disorder due to intrinsic circulating anticoagulants, antibodies, or inhibitors" }, { "from_icd11": "3B21.Z", "icd10_code": "D68311", "icd10_title": "Acquired hemophilia" }, { "from_icd11": "3B21.Z", "icd10_code": "D6831", "icd10_title": "Hemorrhagic disorder due to intrinsic circulating anticoagulants, antibodies, or inhibitors" }, { "from_icd11": "3B21.Z", "icd10_code": "D683", "icd10_title": "Hemorrhagic disorder due to circulating anticoagulants" }, { "from_icd11": "6D11.3", "icd10_code": "F6089", "icd10_title": "Other specific personality disorders" } ]
D8189
Other combined immunodeficiencies
Actinomyces infections have been documented as very difficult to treat. They are typically treated using high-dose penicillin, ceftriaxone, or amoxicillin but symptoms often recur regardless . Oral treatment is usually continued for 1–2 months for mild disease and 6–12 months for severe disease . Severe disease is characterized by significant purulence and formation of fistulous tracts, which this patient did not have . The patient presented in this case was put on amoxicillin to which she responded well evidenced by improving clinical signs and the absence of bacteria in subsequent cultures. She has later put on a longer course of ampicillin after symptom recurrence. In retrospect, it is possible that the patient's risk of recurrence could have been lowered if a high-dose penicillin or amoxicillin, known for its higher bioavailability, had been chosen for subsequent treatment at the time of recurrence. This is because the later testing conducted was less extensive, and the possibility of a remaining Actinomyces spp. infection was not completely ruled out. Although penicillin and amoxicillin are the recommended treatments for actinomycosis, the six-week course of ampicillin administered during the resurgence of symptoms still provided coverage against Actinomyces spp. It is challenging to determine the exact impact as the abscess resolved following marsupialization and treatment with ampicillin.
4.160156
0.836426
sec[2]/p[4]
en
0.999995
PMC10359135
https://doi.org/10.1155/2023/9912910
[ "amoxicillin", "actinomyces", "penicillin", "this", "ampicillin", "recurrence", "which", "course", "infections", "documented" ]
[ { "code": "1C10.Z", "title": "Actinomycosis, unspecified" }, { "code": "1C10.1", "title": "Abdominal actinomycosis" }, { "code": "1C10.Y", "title": "Other specified forms of actinomycosis" }, { "code": "NE60", "title": "Harmful effects of drugs, medicaments or biological substances, not elsewhere classified" }, { "code": "QC44.2", "title": "Personal history of allergy to drugs, medicaments or biological substances" }, { "code": "MG50.70", "title": "Penicillin resistant Neisseria meningitidis" }, { "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" }, { "code": "4A01.03", "title": "Transient hypogammaglobulinaemia of infancy" }, { "code": "MG50.30", "title": "Ampicillin resistant Haemophilus influenzae" } ]
=== ICD-11 CODES FOUND === [1C10.Z] Actinomycosis, unspecified Also known as: Actinomycosis, unspecified | Actinomycosis | actinomycotic infection | actinomycotic infection of unspecified site | actinomycosis NOS [1C10.1] Abdominal actinomycosis Definition: This is a cervicofacial infectious bacterial disease caused by Actinomyces species such as Actinomyces israelii or A. gerencseriae. It can also be caused by Propionibacterium propionicus, and the condition is likely to be polymicrobial aerobic anaerobic infection. Also known as: Abdominal actinomycosis | abdominal actinomycotic infection | ray fungus disease of the intestines | gastrointestinal actinomycosis | Enteritis due to Actinomyces [1C10.Y] Other specified forms of actinomycosis Also known as: Other specified forms of actinomycosis | Myelitis associated with actinomyces | Actinomycotic encephalitis | Actinomycotic meningitis | meningitis due to actinomycosis [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 [QC44.2] Personal history of allergy to drugs, medicaments or biological substances Also known as: Personal history of allergy to drugs, medicaments or biological substances | history of allergy to drugs, medicaments or biological substances | personal history of allergy to medicinal agents | personal history of allergy to medical substances | history of allergy to medicinal agents [MG50.70] Penicillin resistant Neisseria meningitidis Also known as: Penicillin resistant Neisseria meningitidis [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 [4A01.03] Transient hypogammaglobulinaemia of infancy Also known as: Transient hypogammaglobulinaemia of infancy | immunoglobulin maturational delay | THI - [transient hypogammaglobulinaemia of infancy] [MG50.30] Ampicillin resistant Haemophilus influenzae Also known as: Ampicillin resistant Haemophilus influenzae === GRAPH WALKS === --- Walk 1 --- [1C10.Z] Actinomycosis, unspecified --PARENT--> [1C10] Actinomycosis Def: A disease commonly caused by an infection with the gram-positive bacteria Actinomyces. This disease is characterised by painful abscesses in the mouth, lungs, and gastrointestinal tract. Actinomycosis... --EXCLUDES--> [?] Actinomycetoma Def: Actinomycetoma is a chronic progressive subcutaneous infection caused by implantation of aerobic branching actinomycetes through a skin wound. These organisms are filamentous bacteria which live as sa... --- Walk 2 --- [1C10.Z] Actinomycosis, unspecified --PARENT--> [1C10] Actinomycosis Def: A disease commonly caused by an infection with the gram-positive bacteria Actinomyces. This disease is characterised by painful abscesses in the mouth, lungs, and gastrointestinal tract. Actinomycosis... --CHILD--> [1C10.2] Cervicofacial actinomycosis Def: Cervicofacial actinomycosis is the commonest clinical form of actinomycosis, a sporadically occurring endogenous polymicrobial inflammatory process in which fermentative actinomycetes of the genera Ac... --- Walk 3 --- [1C10.1] Abdominal actinomycosis Def: This is a cervicofacial infectious bacterial disease caused by Actinomyces species such as Actinomyces israelii or A. gerencseriae. It can also be caused by Propionibacterium propionicus, and the cond... --PARENT--> [1C10] Actinomycosis Def: A disease commonly caused by an infection with the gram-positive bacteria Actinomyces. This disease is characterised by painful abscesses in the mouth, lungs, and gastrointestinal tract. Actinomycosis... --CHILD--> [1C10.1] Abdominal actinomycosis Def: This is a cervicofacial infectious bacterial disease caused by Actinomyces species such as Actinomyces israelii or A. gerencseriae. It can also be caused by Propionibacterium propionicus, and the cond... --- Walk 4 --- [1C10.1] Abdominal actinomycosis Def: This is a cervicofacial infectious bacterial disease caused by Actinomyces species such as Actinomyces israelii or A. gerencseriae. It can also be caused by Propionibacterium propionicus, and the cond... --PARENT--> [1C10] Actinomycosis Def: A disease commonly caused by an infection with the gram-positive bacteria Actinomyces. This disease is characterised by painful abscesses in the mouth, lungs, and gastrointestinal tract. Actinomycosis... --CHILD--> [1C10.2] Cervicofacial actinomycosis Def: Cervicofacial actinomycosis is the commonest clinical form of actinomycosis, a sporadically occurring endogenous polymicrobial inflammatory process in which fermentative actinomycetes of the genera Ac... --- Walk 5 --- [1C10.Y] Other specified forms of actinomycosis --PARENT--> [1C10] Actinomycosis Def: A disease commonly caused by an infection with the gram-positive bacteria Actinomyces. This disease is characterised by painful abscesses in the mouth, lungs, and gastrointestinal tract. Actinomycosis... --EXCLUDES--> [?] Actinomycetoma Def: Actinomycetoma is a chronic progressive subcutaneous infection caused by implantation of aerobic branching actinomycetes through a skin wound. These organisms are filamentous bacteria which live as sa... --- Walk 6 --- [1C10.Y] Other specified forms of actinomycosis --PARENT--> [1C10] Actinomycosis Def: A disease commonly caused by an infection with the gram-positive bacteria Actinomyces. This disease is characterised by painful abscesses in the mouth, lungs, and gastrointestinal tract. Actinomycosis... --EXCLUDES--> [?] Actinomycetoma Def: Actinomycetoma is a chronic progressive subcutaneous infection caused by implantation of aerobic branching actinomycetes through a skin wound. These organisms are filamentous bacteria which live as sa...
[ "[1C10.Z] Actinomycosis, unspecified\n --PARENT--> [1C10] Actinomycosis\n Def: A disease commonly caused by an infection with the gram-positive bacteria Actinomyces. This disease is characterised by painful abscesses in the mouth, lungs, and gastrointestinal tract. Actinomycosis...\n --EXCLUDES--> [?] Actinomycetoma\n Def: Actinomycetoma is a chronic progressive subcutaneous infection caused by implantation of aerobic branching actinomycetes through a skin wound. These organisms are filamentous bacteria which live as sa...", "[1C10.Z] Actinomycosis, unspecified\n --PARENT--> [1C10] Actinomycosis\n Def: A disease commonly caused by an infection with the gram-positive bacteria Actinomyces. This disease is characterised by painful abscesses in the mouth, lungs, and gastrointestinal tract. Actinomycosis...\n --CHILD--> [1C10.2] Cervicofacial actinomycosis\n Def: Cervicofacial actinomycosis is the commonest clinical form of actinomycosis, a sporadically occurring endogenous polymicrobial inflammatory process in which fermentative actinomycetes of the genera Ac...", "[1C10.1] Abdominal actinomycosis\n Def: This is a cervicofacial infectious bacterial disease caused by Actinomyces species such as Actinomyces israelii or A. gerencseriae. It can also be caused by Propionibacterium propionicus, and the cond...\n --PARENT--> [1C10] Actinomycosis\n Def: A disease commonly caused by an infection with the gram-positive bacteria Actinomyces. This disease is characterised by painful abscesses in the mouth, lungs, and gastrointestinal tract. Actinomycosis...\n --CHILD--> [1C10.1] Abdominal actinomycosis\n Def: This is a cervicofacial infectious bacterial disease caused by Actinomyces species such as Actinomyces israelii or A. gerencseriae. It can also be caused by Propionibacterium propionicus, and the cond...", "[1C10.1] Abdominal actinomycosis\n Def: This is a cervicofacial infectious bacterial disease caused by Actinomyces species such as Actinomyces israelii or A. gerencseriae. It can also be caused by Propionibacterium propionicus, and the cond...\n --PARENT--> [1C10] Actinomycosis\n Def: A disease commonly caused by an infection with the gram-positive bacteria Actinomyces. This disease is characterised by painful abscesses in the mouth, lungs, and gastrointestinal tract. Actinomycosis...\n --CHILD--> [1C10.2] Cervicofacial actinomycosis\n Def: Cervicofacial actinomycosis is the commonest clinical form of actinomycosis, a sporadically occurring endogenous polymicrobial inflammatory process in which fermentative actinomycetes of the genera Ac...", "[1C10.Y] Other specified forms of actinomycosis\n --PARENT--> [1C10] Actinomycosis\n Def: A disease commonly caused by an infection with the gram-positive bacteria Actinomyces. This disease is characterised by painful abscesses in the mouth, lungs, and gastrointestinal tract. Actinomycosis...\n --EXCLUDES--> [?] Actinomycetoma\n Def: Actinomycetoma is a chronic progressive subcutaneous infection caused by implantation of aerobic branching actinomycetes through a skin wound. These organisms are filamentous bacteria which live as sa...", "[1C10.Y] Other specified forms of actinomycosis\n --PARENT--> [1C10] Actinomycosis\n Def: A disease commonly caused by an infection with the gram-positive bacteria Actinomyces. This disease is characterised by painful abscesses in the mouth, lungs, and gastrointestinal tract. Actinomycosis...\n --EXCLUDES--> [?] Actinomycetoma\n Def: Actinomycetoma is a chronic progressive subcutaneous infection caused by implantation of aerobic branching actinomycetes through a skin wound. These organisms are filamentous bacteria which live as sa..." ]
1C10.Z
Actinomycosis, unspecified
[ { "from_icd11": "1C10.Z", "icd10_code": "A4289", "icd10_title": "Other forms of actinomycosis" }, { "from_icd11": "1C10.Z", "icd10_code": "A4281", "icd10_title": "Actinomycotic meningitis" }, { "from_icd11": "1C10.Z", "icd10_code": "A4282", "icd10_title": "Actinomycotic encephalitis" }, { "from_icd11": "1C10.Z", "icd10_code": "A429", "icd10_title": "Actinomycosis, unspecified" }, { "from_icd11": "1C10.Z", "icd10_code": "A427", "icd10_title": "Actinomycotic sepsis" }, { "from_icd11": "1C10.Z", "icd10_code": "A30-A49", "icd10_title": "" }, { "from_icd11": "1C10.Z", "icd10_code": "A42", "icd10_title": "Actinomycosis" }, { "from_icd11": "1C10.Z", "icd10_code": "A428", "icd10_title": "Other forms of actinomycosis" }, { "from_icd11": "1C10.1", "icd10_code": "A421", "icd10_title": "Abdominal actinomycosis" }, { "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" } ]
A4289
Other forms of actinomycosis
After a multidisciplinary discussion the decision was made to address the SVC, after which he was taken to the bronchoscopy suite for placement of a tracheal stent. Due to the patient’s intolerance of supine positioning and high risk for general anesthesia due to central airway occlusion (CAO), he was placed in the right lateral semi sitting position (45°) with moderate sedation consisting of midazolam 2°mg and dexmedetomidine (DEX) between rate of 1.2–1.8°mcg/kg/h for a total of 40°mcg . Nebulized tetracaine 0.25%/Epinephrine 0.003% was given pre-procedurally. A flexible bronchoscope was introduced through the mouth and into the trachea where 10mL tetracaine 0.25%/Epinephrine 0.003% was injected transtracheally and also liberally applied topically. Significant tracheal deviation/narrowing due to external compression of the trachea was observed. There was a 5°cm long segment of tracheal narrowing secondary to external compression with a lumen around 4°mm in the distal end of the trachea. Ahead of placement of rigid bronchoscope, 20°mg propfol was given intravenously. While still breathing spontaneously, a 16 × 60°mm Ultraflex metallic stent was deployed in the distal trachea with significant improvement of tracheal diameter to 70% of normal . The patient tolerated the procedure without complication and noted immediate improvement in his respiratory status including tolerating a supine position .
3.816406
0.968262
sec[1]/p[1]
en
0.999996
PMC10415654
https://doi.org/10.1016/j.heliyon.2023.e18678
[ "tracheal", "trachea", "placement", "stent", "supine", "position", "tetracaine", "epinephrine", "bronchoscope", "narrowing" ]
[ { "code": "CA05.1", "title": "Acute tracheitis" }, { "code": "CA0Y", "title": "Other specified upper respiratory tract disorders" }, { "code": "LA73.Z", "title": "Structural developmental anomalies of trachea, unspecified" }, { "code": "2F91.1", "title": "Neoplasms of unknown behaviour of trachea, bronchus or lung" }, { "code": "LA73.0", "title": "Congenital stenosis of trachea" }, { "code": "QC2Y", "title": "Other specified contact with health services associated with the health of others" }, { "code": "PK91.10", "title": "Cardiovascular devices associated with injury or harm, pacemaker" }, { "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" } ]
=== ICD-11 CODES FOUND === [CA05.1] Acute tracheitis Definition: This condition refers to the acute inflammation of the trachea. Also known as: Acute tracheitis | acute tracheitis NOS | tracheitis NOS | tracheal inflammation | Acute catarrhal tracheitis Excludes: Chronic tracheitis [CA0Y] Other specified upper respiratory tract disorders Also known as: Other specified upper respiratory tract disorders | Acute adenoiditis | adenoid infection | Pharyngotonsillitis | tonsillopharyngitis [LA73.Z] Structural developmental anomalies of trachea, unspecified Also known as: Structural developmental anomalies of trachea, unspecified | Structural developmental anomalies of trachea | Malformations of trachea | tracheal deformity | tracheal anomaly [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 [LA73.0] Congenital stenosis of trachea Definition: Tracheal stenosis is a fixed intrinsic narrowing of the trachea. The narrowing can be localised to a short or long tracheal segment, often due to a complete tracheal ring. Alternatively, the tracheal lumen may become progressively narrow caudally. Also known as: Congenital stenosis of trachea | tracheal atresia | Atresia of trachea | congenital trachea stricture Includes: Atresia of trachea [QC2Y] Other specified contact with health services associated with the health of others Also known as: Other specified contact with health services associated with the health of others | Boarder in health-care facility other than healthy person accompanying sick person | Health supervision or care of other healthy infant or child | child in care | healthy infant receiving care [PK91.10] Cardiovascular devices associated with injury or harm, pacemaker Also known as: Cardiovascular devices associated with injury or harm, pacemaker | Cardiovascular devices associated with injury or harm, infection following placement of cardiac pacemaker | Cardiac pacemaker malfunction | Mechanical complication of cardiac pacemaker | Malfunction of artificial pacing Excludes: Pacemaker or implantable cardioverter defibrillator battery at end of battery life | Circumstances associated with a surgical or other medical device influencing the episode of care without injury or harm [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 === GRAPH WALKS === --- Walk 1 --- [CA05.1] Acute tracheitis Def: This condition refers to the acute inflammation of the trachea.... --RELATED_TO--> [?] Neonatal tracheitis Def: A disease of the trachea in neonates, caused by an infection with a bacterial, viral, or fungal source. This disease is characterised by stridor, or increased respiratory effort. Transmission is commo... --PARENT--> [?] Neonatal infections involving respiratory system --- Walk 2 --- [CA05.1] Acute tracheitis Def: This condition refers to the acute inflammation of the trachea.... --EXCLUDES--> [?] Chronic bronchitis --EXCLUDES--> [?] Certain specified chronic obstructive pulmonary disease --- Walk 3 --- [CA0Y] Other specified upper respiratory tract disorders --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 4 --- [CA0Y] Other specified upper respiratory tract disorders --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 ... --PARENT--> [12] Diseases of the respiratory system --- Walk 5 --- [LA73.Z] Structural developmental anomalies of trachea, unspecified --PARENT--> [LA73] Structural developmental anomalies of trachea --CHILD--> [LA73.1] Congenital tracheomalacia Def: Congenital tracheomalacia is a relatively uncommon anomaly that results from an intrinsic weakness of the cartilaginous support of the trachea such that it is prone to collapse especially during expir... --- Walk 6 --- [LA73.Z] Structural developmental anomalies of trachea, unspecified --PARENT--> [LA73] Structural developmental anomalies of trachea --CHILD--> [LA73.Y] Other specified structural developmental anomalies of trachea
[ "[CA05.1] Acute tracheitis\n Def: This condition refers to the acute inflammation of the trachea....\n --RELATED_TO--> [?] Neonatal tracheitis\n Def: A disease of the trachea in neonates, caused by an infection with a bacterial, viral, or fungal source. This disease is characterised by stridor, or increased respiratory effort. Transmission is commo...\n --PARENT--> [?] Neonatal infections involving respiratory system", "[CA05.1] Acute tracheitis\n Def: This condition refers to the acute inflammation of the trachea....\n --EXCLUDES--> [?] Chronic bronchitis\n --EXCLUDES--> [?] Certain specified chronic obstructive pulmonary disease", "[CA0Y] Other specified upper respiratory tract disorders\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...", "[CA0Y] Other specified upper respiratory tract disorders\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 --PARENT--> [12] Diseases of the respiratory system", "[LA73.Z] Structural developmental anomalies of trachea, unspecified\n --PARENT--> [LA73] Structural developmental anomalies of trachea\n --CHILD--> [LA73.1] Congenital tracheomalacia\n Def: Congenital tracheomalacia is a relatively uncommon anomaly that results from an intrinsic weakness of the cartilaginous support of the trachea such that it is prone to collapse especially during expir...", "[LA73.Z] Structural developmental anomalies of trachea, unspecified\n --PARENT--> [LA73] Structural developmental anomalies of trachea\n --CHILD--> [LA73.Y] Other specified structural developmental anomalies of trachea" ]
CA05.1
Acute tracheitis
[ { "from_icd11": "CA05.1", "icd10_code": "J0410", "icd10_title": "Acute tracheitis without obstruction" }, { "from_icd11": "CA05.1", "icd10_code": "J0411", "icd10_title": "Acute tracheitis with obstruction" }, { "from_icd11": "CA05.1", "icd10_code": "J041", "icd10_title": "Acute tracheitis" }, { "from_icd11": "LA73.Z", "icd10_code": "Q321", "icd10_title": "Other congenital malformations of trachea" }, { "from_icd11": "LA73.Z", "icd10_code": "Q32", "icd10_title": "Congenital malformations of trachea and bronchus" }, { "from_icd11": "2F91.1", "icd10_code": "D381", "icd10_title": "Neoplasm of uncertain behavior of trachea, bronchus and lung" }, { "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" } ]
J0410
Acute tracheitis without obstruction
A 58-year-old female patient first presented to our medical center in 2010, who had no significant past medical history and presented with repeated external urethral orifice itching over the previous 1 year and with painless occasional urethral bleeding over the previous 3 months. Vaginal examination showed a pedicled mass measuring approximately 1.0 × 1.5 cm at the external urethral orifice at 11 o’clock position, with ulcerated bleeding on the surface, obvious tenderness, and medium texture. No enlarged inguinal lymph nodes were palpated. The results of serum projects were in the normal range and urinalysis showed a large number of red blood cells per high power field. A puncture biopsy of the mass showed villiform adenocarcinoma (mild to moderate atypia) before admission in a local hospital. The patient underwent urethral orifice tumor resection under local infiltration anesthesia. Subsequent routine pathology confirmed the urethral adenocarcinoma with mucinous features (moderate atypia) . The patient recovered without complications, maintained normal urination function, and did not receive other adjuvant therapy due to the current localised TNM stage (T1N0M0). However, during a postoperative 5-years follow-up time of case 2, the periodic routine follow-up examinations was not properly conducted, which was not enough to determine whether the patient had local recurrence or distant metastasis.
3.816406
0.985352
sec[1]/sec[1]/p[0]
en
0.999997
36676733
https://doi.org/10.3390/medicina59010109
[ "urethral", "orifice", "local", "over", "bleeding", "adenocarcinoma", "atypia", "routine", "center", "past" ]
[ { "code": "GC0Y", "title": "Other diseases of urinary system" }, { "code": "GC02.Z", "title": "Urethritis and urethral syndrome, unspecified" }, { "code": "GC02.Y", "title": "Other specified urethritis and urethral syndrome" }, { "code": "GC03", "title": "Urethral stricture" }, { "code": "LB31.C", "title": "Congenital absence of bladder or urethra" }, { "code": "GC01.Y", "title": "Other specified disorders of bladder" }, { "code": "LA87.1Y", "title": "Other specified congenital anomaly of mitral valve" }, { "code": "LA87.0Y", "title": "Other specified congenital anomaly of tricuspid valve" }, { "code": "DA20.0", "title": "Oesophageal obstruction" }, { "code": "LA8C.Y", "title": "Other specified congenital anomaly of coronary artery" } ]
=== ICD-11 CODES FOUND === [GC0Y] Other diseases of urinary system Also known as: Other diseases of urinary system | Acquired urethral deformity, not elsewhere classified | acquired urethral deformity NOS | Urethral bleeding | bleeding from urethra [GC02.Z] Urethritis and urethral syndrome, unspecified Also known as: Urethritis and urethral syndrome, unspecified | Urethritis and urethral syndrome | urethral syndrome NOS | urethra syndrome [GC02.Y] Other specified urethritis and urethral syndrome Also known as: Other specified urethritis and urethral syndrome | Other urethritis | inflammation of urethra | paraurethritis | periurethritis [GC03] Urethral stricture Definition: Stenosis of the urethra accompanied by fibrosis and scarring of the spongiosal body Also known as: Urethral stricture | ankylurethria | urethral stenosis | urethral contracture | urethral obstruction [LB31.C] Congenital absence of bladder or urethra Definition: Any condition caused by failure of both the bladder and the urethra to develop during the antenatal period. This condition may result in fetal death, or sepsis and sever complications in cases of live births. Also known as: Congenital absence of bladder or urethra | Congenital absence of bladder | acystia | agenesis of bladder | Congenital absence of urethra [GC01.Y] Other specified disorders of bladder Also known as: Other specified disorders of bladder | Non-neurogenic neurogenic bladder | Occult neuropathic bladder | Hinman syndrome | Hinman-Allen syndrome [LA87.1Y] Other specified congenital anomaly of mitral valve Also known as: Other specified congenital anomaly of mitral valve | Mitral annular hypoplasia | hypoplasia of mitral valvar annulus | hypoplasia of the mitral annulus | Straddling mitral valve [LA87.0Y] Other specified congenital anomaly of tricuspid valve Also known as: Other specified congenital anomaly of tricuspid valve | Tricuspid annular hypoplasia | hypoplasia of the tricuspid annulus | hypoplasia of tricuspid valvar annulus | Straddling tricuspid valve [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 [LA8C.Y] Other specified congenital anomaly of coronary artery Also known as: Other specified congenital anomaly of coronary artery | Myocardial bridging of coronary artery | myocardial bridge | Congenital coronary arterial orifice stenosis | congenital coronary stricture Includes: Congenital coronary arterial aneurysm === GRAPH WALKS === --- Walk 1 --- [GC0Y] Other diseases of urinary system --PARENT--> [?] Certain specified diseases of urinary system --EXCLUDES--> [?] 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 2 --- [GC0Y] Other diseases of urinary system --PARENT--> [?] Certain specified diseases of urinary system --RELATED_TO--> [?] Urinary incontinence Def: Any condition of the urinary system, caused by determinants arising during the antenatal period or after birth, leading to loss of voluntary control or support of the urethra. These conditions are cha... --- Walk 3 --- [GC02.Z] Urethritis and urethral syndrome, unspecified --PARENT--> [GC02] Urethritis and urethral syndrome Def: A condition of the urethra, caused by non-infectious factors such as trauma, allergies, anatomical malformations, or scarring and adhesions following a medical intervention. This condition is characte... --CHILD--> [GC02.Y] Other specified urethritis and urethral syndrome --- Walk 4 --- [GC02.Z] Urethritis and urethral syndrome, unspecified --PARENT--> [GC02] Urethritis and urethral syndrome Def: A condition of the urethra, caused by non-infectious factors such as trauma, allergies, anatomical malformations, or scarring and adhesions following a medical intervention. This condition is characte... --EXCLUDES--> [?] Predominantly sexually transmitted infections --- Walk 5 --- [GC02.Y] Other specified urethritis and urethral syndrome --PARENT--> [GC02] Urethritis and urethral syndrome Def: A condition of the urethra, caused by non-infectious factors such as trauma, allergies, anatomical malformations, or scarring and adhesions following a medical intervention. This condition is characte... --RELATED_TO--> [?] Infections of urethra in pregnancy Def: Urethra infections occurring during pregnancy... --- Walk 6 --- [GC02.Y] Other specified urethritis and urethral syndrome --PARENT--> [GC02] Urethritis and urethral syndrome Def: A condition of the urethra, caused by non-infectious factors such as trauma, allergies, anatomical malformations, or scarring and adhesions following a medical intervention. This condition is characte... --PARENT--> [?] Certain specified diseases of urinary system
[ "[GC0Y] Other diseases of urinary system\n --PARENT--> [?] Certain specified diseases of urinary system\n --EXCLUDES--> [?] 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...", "[GC0Y] Other diseases of urinary system\n --PARENT--> [?] Certain specified diseases of urinary system\n --RELATED_TO--> [?] Urinary incontinence\n Def: Any condition of the urinary system, caused by determinants arising during the antenatal period or after birth, leading to loss of voluntary control or support of the urethra. These conditions are cha...", "[GC02.Z] Urethritis and urethral syndrome, unspecified\n --PARENT--> [GC02] Urethritis and urethral syndrome\n Def: A condition of the urethra, caused by non-infectious factors such as trauma, allergies, anatomical malformations, or scarring and adhesions following a medical intervention. This condition is characte...\n --CHILD--> [GC02.Y] Other specified urethritis and urethral syndrome", "[GC02.Z] Urethritis and urethral syndrome, unspecified\n --PARENT--> [GC02] Urethritis and urethral syndrome\n Def: A condition of the urethra, caused by non-infectious factors such as trauma, allergies, anatomical malformations, or scarring and adhesions following a medical intervention. This condition is characte...\n --EXCLUDES--> [?] Predominantly sexually transmitted infections", "[GC02.Y] Other specified urethritis and urethral syndrome\n --PARENT--> [GC02] Urethritis and urethral syndrome\n Def: A condition of the urethra, caused by non-infectious factors such as trauma, allergies, anatomical malformations, or scarring and adhesions following a medical intervention. This condition is characte...\n --RELATED_TO--> [?] Infections of urethra in pregnancy\n Def: Urethra infections occurring during pregnancy...", "[GC02.Y] Other specified urethritis and urethral syndrome\n --PARENT--> [GC02] Urethritis and urethral syndrome\n Def: A condition of the urethra, caused by non-infectious factors such as trauma, allergies, anatomical malformations, or scarring and adhesions following a medical intervention. This condition is characte...\n --PARENT--> [?] Certain specified diseases of urinary system" ]
GC0Y
Other diseases of urinary system
[ { "from_icd11": "GC02.Z", "icd10_code": "N342", "icd10_title": "Other urethritis" }, { "from_icd11": "GC02.Z", "icd10_code": "N343", "icd10_title": "Urethral syndrome, unspecified" }, { "from_icd11": "GC02.Z", "icd10_code": "N34", "icd10_title": "Urethritis and urethral syndrome" }, { "from_icd11": "GC03", "icd10_code": "N35014", "icd10_title": "Post-traumatic urethral stricture, male, unspecified" }, { "from_icd11": "GC03", "icd10_code": "N35919", "icd10_title": "Unspecified urethral stricture, male, unspecified site" }, { "from_icd11": "GC03", "icd10_code": "N35911", "icd10_title": "Unspecified urethral stricture, male, meatal" }, { "from_icd11": "GC03", "icd10_code": "N35912", "icd10_title": "Unspecified bulbous urethral stricture, male" }, { "from_icd11": "GC03", "icd10_code": "N35819", "icd10_title": "Other urethral stricture, male, unspecified site" }, { "from_icd11": "GC03", "icd10_code": "N3592", "icd10_title": "Unspecified urethral stricture, female" }, { "from_icd11": "GC03", "icd10_code": "N3582", "icd10_title": "Other urethral stricture, female" }, { "from_icd11": "GC03", "icd10_code": "N35812", "icd10_title": "Other urethral bulbous stricture, male" }, { "from_icd11": "GC03", "icd10_code": "N35028", "icd10_title": "Other post-traumatic urethral stricture, female" }, { "from_icd11": "GC03", "icd10_code": "N35111", "icd10_title": "Postinfective urethral stricture, not elsewhere classified, male, meatal" }, { "from_icd11": "GC03", "icd10_code": "N359", "icd10_title": "Urethral stricture, unspecified" }, { "from_icd11": "GC03", "icd10_code": "N358", "icd10_title": "Other urethral stricture" } ]
N342
Other urethritis
Clinicians need to remain cognisant of alternative diagnoses to malignancy and have a heightened index of suspicion in patients with large colonic masses with multi-organ involvement. Confirmation of a benign diagnosis, such as actinomycosis, may reduce surgical morbidity by affording less radical resection when possible. Interestingly, non-operative therapy with long course antibiotics (6–12-months) is well described for actinomycosis but has limited utility when unable to effectively rule out malignancy . Unfortunately, the presence of large abscesses not amenable to percutaneous drainage or soft tissue necrosis, for which the condition is notorious, often necessitate operative intervention . As performed in the index case, en bloc resection is often necessary given a presumptive pre-operative diagnosis of locally advanced cancer. Following surgery, in contrast to the aforementioned conservative treatment, there is far less consensus on the duration of antibiotics , . Proposed regimes vary widely not only in duration but also in choice of agent, dosage, pelvic versus abdominal involvement, as well as clinical response . There is no role for chemotherapy in the treatment of this infectious condition. We opted for a short course of antibiotics with close clinical follow-up as our patient had no known risk factors and had been doing well off antibiotic therapy while awaiting final histopathology.
4.171875
0.63623
sec[2]/p[1]
en
0.999998
36907045
https://doi.org/10.1016/j.ijscr.2023.107957
[ "antibiotics", "well", "malignancy", "index", "large", "involvement", "actinomycosis", "less", "resection", "course" ]
[ { "code": "NE60", "title": "Harmful effects of drugs, medicaments or biological substances, not elsewhere classified" }, { "code": "MG50.9Z", "title": "Salmonella resistant to unspecified antibiotic" }, { "code": "MG50.AZ", "title": "Shigella resistant to unspecified antibiotic" }, { "code": "MG50.BZ", "title": "Vibrio resistant to unspecified antibiotic" }, { "code": "QC05.Y", "title": "Other specified prophylactic measures" }, { "code": "EB30", "title": "Eosinophilic cellulitis" }, { "code": "QC2Y", "title": "Other specified contact with health services associated with the health of others" }, { "code": "4A60.1", "title": "Cryopyrin-associated periodic syndromes" }, { "code": "2D10.0", "title": "Follicular carcinoma of thyroid gland" }, { "code": "2B5H", "title": "Well differentiated lipomatous tumour, primary site" } ]
=== 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 [MG50.9Z] Salmonella resistant to unspecified antibiotic Also known as: Salmonella resistant to unspecified antibiotic | Antibiotic resistant Salmonella [MG50.AZ] Shigella resistant to unspecified antibiotic Also known as: Shigella resistant to unspecified antibiotic | Antibiotic resistant Shigella [MG50.BZ] Vibrio resistant to unspecified antibiotic Also known as: Vibrio resistant to unspecified antibiotic | Antibiotic resistant Vibrio [QC05.Y] Other specified prophylactic measures Also known as: Other specified prophylactic measures | Other prophylactic chemotherapy | chemoprophylaxis | prophylactic chemotherapy | Systemic prophylactic chemotherapy [EB30] Eosinophilic cellulitis Definition: Eosinophilic cellulitis (Wells syndrome) is characterised by a distinctive clinical picture resembling cellulitis, and a typical histology with tissue eosinophilia, oedema and ‘flame’ figures (clusters of eosinophils and histiocytes around a core of collagen and eosinophilic debris). It can affect either sex, usually in adult life. Any site may be involved, with single or multiple lesions, and recurrences are common. Initially, the lesions are itchy erythematous plaques with features resembling Also known as: Eosinophilic cellulitis | Wells' syndrome [QC2Y] Other specified contact with health services associated with the health of others Also known as: Other specified contact with health services associated with the health of others | Boarder in health-care facility other than healthy person accompanying sick person | Health supervision or care of other healthy infant or child | child in care | healthy infant receiving care [4A60.1] Cryopyrin-associated periodic syndromes Definition: 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 signs and symptoms of inflammation in the form of rash, fever, joint and eye symptoms with increased acute phase reactants. Also known as: Cryopyrin-associated periodic syndromes | CAPS - [Cryopyrin-associated periodic syndromes] | Cryopyrinopathies | Chronic infantile neurological, cutaneous and articular syndrome | Infantile-onset multisystem inflammatory disease Includes: Cryopyrinopathies [2D10.0] Follicular carcinoma of thyroid gland Definition: A differentiated adenocarcinoma arising from the follicular cells of the thyroid gland. The nuclear features which characterise the thyroid gland papillary carcinoma are absent. Radiation exposure is a risk factor and it comprises approximately 10% to 15% of thyroid cancers. Clinically, it usually presents as a solitary mass in the thyroid gland. It is generally unifocal and thickly encapsulated and shows invasion of the capsule or the vessels. Diagnostic procedures include: thyroid ultrasound a Also known as: Follicular carcinoma of thyroid gland | follicular carcinoma of unspecified site | follicular thyroid carcinoma | moderately differentiated follicular carcinoma of thyroid gland | pure follicle carcinoma of thyroid gland [2B5H] Well differentiated lipomatous tumour, primary site Also known as: Well differentiated lipomatous tumour, primary site | Atypical liposarcoma === GRAPH WALKS === --- Walk 1 --- [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 substance use Def: Disorders due to substance use include disorders that result from a single occasion or repeated use of substances that have psychoactive properties, including certain medications. Disorders related to... --- Walk 2 --- [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--> [?] Possession trance disorder Def: Possession trance disorder is characterised by trance states in which there is a marked alteration in the individual’s state of consciousness and the individual’s customary sense of personal identity ... --- Walk 3 --- [MG50.9Z] Salmonella resistant to unspecified antibiotic --PARENT--> [MG50.9] Antibiotic resistant Salmonella --CHILD--> [MG50.91] Third generation cephalosporin resistant Salmonella --- Walk 4 --- [MG50.9Z] Salmonella resistant to unspecified antibiotic --PARENT--> [MG50.9] Antibiotic resistant Salmonella --CHILD--> [MG50.92] Carbapenem resistant Salmonella --- Walk 5 --- [MG50.AZ] Shigella resistant to unspecified antibiotic --PARENT--> [MG50.A] Antibiotic resistant Shigella --CHILD--> [MG50.A1] Fluoroquinolone resistant Shigella --- Walk 6 --- [MG50.AZ] Shigella resistant to unspecified antibiotic --PARENT--> [MG50.A] Antibiotic resistant Shigella --CHILD--> [MG50.A2] Third-generation cephalosporins resistant Shigella
[ "[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 substance use\n Def: Disorders due to substance use include disorders that result from a single occasion or repeated use of substances that have psychoactive properties, including certain medications. Disorders related to...", "[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--> [?] Possession trance disorder\n Def: Possession trance disorder is characterised by trance states in which there is a marked alteration in the individual’s state of consciousness and the individual’s customary sense of personal identity ...", "[MG50.9Z] Salmonella resistant to unspecified antibiotic\n --PARENT--> [MG50.9] Antibiotic resistant Salmonella\n --CHILD--> [MG50.91] Third generation cephalosporin resistant Salmonella", "[MG50.9Z] Salmonella resistant to unspecified antibiotic\n --PARENT--> [MG50.9] Antibiotic resistant Salmonella\n --CHILD--> [MG50.92] Carbapenem resistant Salmonella", "[MG50.AZ] Shigella resistant to unspecified antibiotic\n --PARENT--> [MG50.A] Antibiotic resistant Shigella\n --CHILD--> [MG50.A1] Fluoroquinolone resistant Shigella", "[MG50.AZ] Shigella resistant to unspecified antibiotic\n --PARENT--> [MG50.A] Antibiotic resistant Shigella\n --CHILD--> [MG50.A2] Third-generation cephalosporins resistant Shigella" ]
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 patient initially presented with normal platelet count and with normal mentation. The patient did not have any previous issues relating to any hematologic disorders. The rapid onset of thrombocytopenia and renal failure in the context of severe COVID19 infection raised the concern for possible thrombocytopenia induced by consumptive process due to her underlying infection. In addition, COVID19‐induced thrombotic angiopathy without TTP was also considered on account of the patient's coagulopathic and inflammatory changes. The presence of a significant number of schistocytes on peripheral smear raised the concern for thrombotic thrombocytopenic purpura (TTP), despite initial presentation with normal platelet count and concurrent COVID19 infection. Due to high clinical and laboratory suspicion for TTP, plasma exchange with FFP was initiated with pending ADAMTS13 results. The patient experienced a significant improvement in her clinical status, biochemically, by laboratory values and with significant decrease in schistocytes observed per high power field. The patient's coagulation profile was not consistent with disseminated intravascular coagulation (DIC). On account of normal ADAMTS13 levels, yet clear laboratory and pathologic evidence of a thrombotic microangiopathy, our patient was diagnosed with COVID19‐induced thrombotic angiopathy, which responded briskly to plasma exchange intervention.
4
0.978516
sec[1]/p[0]
en
0.999997
34853683
https://doi.org/10.1002/ccr3.4991
[ "thrombotic", "infection", "induced", "laboratory", "platelet", "count", "thrombocytopenia", "raised", "concern", "angiopathy" ]
[ { "code": "DD30.Z", "title": "Acute vascular disorders of intestine, unspecified" }, { "code": "JA61.Y", "title": "Other specified venous complications in pregnancy" }, { "code": "JB41.Y", "title": "Other specified venous complications in the puerperium" }, { "code": "BA41.Z", "title": "Acute myocardial infarction, unspecified" }, { "code": "DB61", "title": "Perianal venous thrombosis" }, { "code": "1H0Z", "title": "Infection, unspecified" }, { "code": "1G40", "title": "Sepsis without septic shock" }, { "code": "FA10.Z", "title": "Direct infections of joint, unspecified" }, { "code": "1D9Z", "title": "Unspecified viral infection of unspecified site" }, { "code": "1A40.Z", "title": "Infectious gastroenteritis or colitis without specification of infectious agent" } ]
=== ICD-11 CODES FOUND === [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 [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 [JB41.Y] Other specified venous complications in the puerperium Also known as: Other specified venous complications in the puerperium | Genital varices in the puerperium | varix of vulva in puerperium | Postpartum varicose veins of legs | varicose veins of legs in the puerperium [BA41.Z] Acute myocardial infarction, unspecified Also known as: Acute myocardial infarction, unspecified | Acute myocardial infarction | cardiac attack | heart attack | acute cardiac infarction [DB61] Perianal venous thrombosis Definition: Extremely painful cherry like lesions under the perianal skin containing clotted blood have been attributed to rupture of a blood vessel with haematoma. However, histology confirmed that these lesions are thrombi lying within the thin-walled vessels of the external anal plexus. Also known as: Perianal venous thrombosis | thrombosed external pile | anal thrombosis | Perianal haematoma (nontraumatic) | perianal thrombosis Includes: perianal thrombosis | Perianal haematoma (nontraumatic) [1H0Z] Infection, unspecified Also known as: Infection, unspecified | infection NOS | infectious disease NOS | infection unknown | infection process NOS [1G40] Sepsis without septic shock Definition: Sepsis is defined as a life-threatening organ dysfunction caused by a dysregulated host response to infection. Also known as: Sepsis without septic shock | sepsis without septic shock with known organism | Sepsis-associated hypotension | Unspecified sepsis | general septic intoxication Excludes: Septicaemia | Sepsis of fetus or newborn [FA10.Z] Direct infections of joint, unspecified Also known as: Direct infections of joint, unspecified | Direct infections of joint | septic arthritis | pyogenic arthritis | arthritis due to infection [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 [1A40.Z] Infectious gastroenteritis or colitis without specification of infectious agent Also known as: Infectious gastroenteritis or colitis without specification of infectious agent | Gastroenteritis or colitis without specification of infectious agent | diarrhoea and gastroenteritis of presumed infectious origin | diarrhoeal enteritis | GE - [gastroenteritis] === GRAPH WALKS === --- Walk 1 --- [DD30.Z] Acute vascular disorders of intestine, unspecified --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.... --RELATED_TO--> [?] 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 ... --- Walk 2 --- [DD30.Z] Acute vascular disorders of intestine, unspecified --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.... --- Walk 3 --- [JA61.Y] Other specified venous complications in pregnancy --PARENT--> [JA61] Venous complications in pregnancy --EXCLUDES--> [?] Complications following abortion, ectopic or molar pregnancy Def: Any complication affecting pregnant females, caused by or subsequent to abortion, ectopic, and molar pregnancy.... --- Walk 4 --- [JA61.Y] Other specified venous complications in pregnancy --PARENT--> [JA61] Venous complications in pregnancy --CHILD--> [JA61.1] Genital varices in pregnancy --- Walk 5 --- [JB41.Y] Other specified venous complications in the puerperium --PARENT--> [JB41] Venous complications in the puerperium --EXCLUDES--> [?] Venous complications in pregnancy --- Walk 6 --- [JB41.Y] Other specified venous complications in the puerperium --PARENT--> [JB41] Venous complications in the puerperium --CHILD--> [JB41.2] Haemorrhoids in the puerperium
[ "[DD30.Z] Acute vascular disorders of intestine, unspecified\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 --RELATED_TO--> [?] 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 ...", "[DD30.Z] Acute vascular disorders of intestine, unspecified\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....", "[JA61.Y] Other specified venous complications in pregnancy\n --PARENT--> [JA61] Venous complications in pregnancy\n --EXCLUDES--> [?] Complications following abortion, ectopic or molar pregnancy\n Def: Any complication affecting pregnant females, caused by or subsequent to abortion, ectopic, and molar pregnancy....", "[JA61.Y] Other specified venous complications in pregnancy\n --PARENT--> [JA61] Venous complications in pregnancy\n --CHILD--> [JA61.1] Genital varices in pregnancy", "[JB41.Y] Other specified venous complications in the puerperium\n --PARENT--> [JB41] Venous complications in the puerperium\n --EXCLUDES--> [?] Venous complications in pregnancy", "[JB41.Y] Other specified venous complications in the puerperium\n --PARENT--> [JB41] Venous complications in the puerperium\n --CHILD--> [JB41.2] Haemorrhoids in the puerperium" ]
DD30.Z
Acute vascular disorders of intestine, unspecified
[ { "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" }, { "from_icd11": "DD30.Z", "icd10_code": "K55021", "icd10_title": "Focal (segmental) acute infarction of small intestine" }, { "from_icd11": "DD30.Z", "icd10_code": "K55039", "icd10_title": "Acute (reversible) ischemia of large intestine, extent unspecified" }, { "from_icd11": "DD30.Z", "icd10_code": "K55059", "icd10_title": "Acute (reversible) ischemia of intestine, part and extent unspecified" }, { "from_icd11": "DD30.Z", "icd10_code": "K55042", "icd10_title": "Diffuse acute infarction of large intestine" }, { "from_icd11": "DD30.Z", "icd10_code": "K55041", "icd10_title": "Focal (segmental) acute infarction of large intestine" }, { "from_icd11": "DD30.Z", "icd10_code": "K55011", "icd10_title": "Focal (segmental) acute (reversible) ischemia of small intestine" }, { "from_icd11": "DD30.Z", "icd10_code": "K55012", "icd10_title": "Diffuse acute (reversible) ischemia of small intestine" }, { "from_icd11": "DD30.Z", "icd10_code": "K55049", "icd10_title": "Acute infarction of large intestine, extent unspecified" }, { "from_icd11": "DD30.Z", "icd10_code": "K55061", "icd10_title": "Focal (segmental) acute infarction of intestine, part unspecified" }, { "from_icd11": "DD30.Z", "icd10_code": "K55022", "icd10_title": "Diffuse acute infarction of small intestine" }, { "from_icd11": "DD30.Z", "icd10_code": "K55031", "icd10_title": "Focal (segmental) acute (reversible) ischemia of large intestine" }, { "from_icd11": "DD30.Z", "icd10_code": "K55032", "icd10_title": "Diffuse acute (reversible) ischemia of large intestine" } ]
K55019
Acute (reversible) ischemia of small intestine, extent unspecified
Meckel’s diverticulum (MD) is the most common congenital anomaly of the intestines. It was first described by the German anatomist Johann Meckel in 1809 as an omphalomesenteric duct remnant . The ‘rule of twos’ is a useful mnemonic for the features of MD although the figures do have a broad range: it occurs in 2% of the population, measures about 2 inches (5 cm) in length, located ~2 feet (60 cm) from the ileocecal valve, may contain two types of tissue (gastric and pancreatic) and it is symptomatic in just 2% of the affected population mostly under the age of 2 years . Hemorrhage and anemia are the most frequent presenting complaint in inverted MD. Others include intestinal obstruction, diverticulitis, Littre hernia or perforation . Adult intussusception because of an inverted MD is exceptionally rare . Preoperative diagnosis of inverted MD is challenging because of overlapping clinical and imaging characteristics. Therefore, it is necessary for surgeons to early recognize its various clinical presentations. Whether diagnosed preoperatively or intraoperatively, surgery remains the mainstay of treatment. Our study presents an adult female presented with a sign of small bowel obstruction because of intussusception of inverted MD that was managed successfully with surgery. The aim of this report is to shed light on this rare entity and to alert surgeons to not oversight MD in the adult population.
4.152344
0.877441
sec[0]/p[0]
en
0.999998
PMC10200354
https://doi.org/10.1093/jscr/rjad288
[ "inverted", "population", "because", "meckel", "obstruction", "intussusception", "rare", "surgeons", "this", "diverticulum" ]
[ { "code": "2F21.Y", "title": "Other specified benign keratinocytic acanthomas" }, { "code": "2F7Z", "title": "Neoplasms of uncertain behaviour of unspecified site" }, { "code": "LD41.P", "title": "Duplications with other complex rearrangements" }, { "code": "QA00.Y", "title": "Other specified general examination or investigation of persons without complaint or reported diagnosis" }, { "code": "QA03.Z", "title": "Routine general health check-up of defined subpopulation, unspecified" }, { "code": "QA03.Y", "title": "Other specified routine general health check-up of defined subpopulation" }, { "code": "QC10", "title": "Procedure not carried out because of contraindication" }, { "code": "QB12.0", "title": "Organ transplant candidate" }, { "code": "QC04.5", "title": "Immunization not carried out because of patient refusal" }, { "code": "QC04.Z", "title": "Immunization not carried out for unspecified reason" } ]
=== ICD-11 CODES FOUND === [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 [2F7Z] Neoplasms of uncertain behaviour of unspecified site Also known as: Neoplasms of uncertain behaviour of unspecified site | Anaemia in neoplastic disease of uncertain behaviour | Brain degeneration in neoplastic disease of uncertain behaviour | Cerebellar ataxia in neoplastic disease of uncertain behaviour | Encephalopathy in neoplastic disease of uncertain behaviour [LD41.P] Duplications with other complex rearrangements Also known as: Duplications with other complex rearrangements | 15q11 duplication or inversion | 8p inverted duplication or deletion | 8p inverted duplication or deletion syndrome | Cat-eye syndrome [QA00.Y] Other specified general examination or investigation of persons without complaint or reported diagnosis Also known as: Other specified general examination or investigation of persons without complaint or reported diagnosis | Examination for period of rapid growth in childhood | evaluation of period of rapid growth in childhood | observation of development state of period of rapid growth in childhood | Examination for adolescent development state [QA03.Z] Routine general health check-up of defined subpopulation, unspecified Also known as: Routine general health check-up of defined subpopulation, unspecified | Routine general health check-up of defined subpopulation [QA03.Y] Other specified routine general health check-up of defined subpopulation Also known as: Other specified routine general health check-up of defined subpopulation | Routine medical examination of refugees | Routine medical examination of students | Routine medical examination of preschool children | Routine medical examination of schoolchildren [QC10] Procedure not carried out because of contraindication Also known as: Procedure not carried out because of contraindication | intervention not carried out because of contraindication | Procedure cancelled due to contraindication [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 [QC04.5] Immunization not carried out because of patient refusal Also known as: Immunization not carried out because of patient refusal [QC04.Z] Immunization not carried out for unspecified reason Also known as: Immunization not carried out for unspecified reason | Immunization not carried out | vaccination not done | Immunization not carried out because of contraindication, not otherwise specified === GRAPH WALKS === --- Walk 1 --- [2F21.Y] Other specified benign keratinocytic acanthomas --PARENT--> [2F21] Benign keratinocytic acanthomas Def: A group of benign discrete epidermal proliferative disorders including seborrhoeic keratosis and clear cell acanthoma.... --CHILD--> [2F21.0] Seborrhoeic keratosis Def: Seborrhoeic keratoses are very common benign neoplasms of epidermal keratinocytes which increase in prevalence and number with age. They are commonly multiple and are very variable in shape and colour... --- Walk 2 --- [2F21.Y] Other specified benign keratinocytic acanthomas --PARENT--> [2F21] Benign keratinocytic acanthomas Def: A group of benign discrete epidermal proliferative disorders including seborrhoeic keratosis and clear cell acanthoma.... --CHILD--> [2F21.0] Seborrhoeic keratosis Def: Seborrhoeic keratoses are very common benign neoplasms of epidermal keratinocytes which increase in prevalence and number with age. They are commonly multiple and are very variable in shape and colour... --- Walk 3 --- [2F7Z] Neoplasms of uncertain behaviour of unspecified site --PARENT--> [?] Neoplasms of uncertain behaviour, except of lymphoid, haematopoietic, central nervous system or related tissues Def: A neoplasm except of lymphoid, haematopoietic, central nervous system or related tissues displaying morphologic, phenotypic, or genotypic characteristics that are clearly not benign but do not permit ... --CHILD--> [2F71] Neoplasms of uncertain behaviour of middle ear, respiratory or intrathoracic organs --- Walk 4 --- [2F7Z] Neoplasms of uncertain behaviour of unspecified site --PARENT--> [?] Neoplasms of uncertain behaviour, except of lymphoid, haematopoietic, central nervous system or related tissues Def: A neoplasm except of lymphoid, haematopoietic, central nervous system or related tissues displaying morphologic, phenotypic, or genotypic characteristics that are clearly not benign but do not permit ... --RELATED_TO--> [?] Pathological fracture in neoplastic disease of uncertain behaviour --- Walk 5 --- [LD41.P] Duplications with other complex rearrangements --PARENT--> [LD41] Duplications of the autosomes --CHILD--> [LD41.1] Duplications of chromosome 2 --- Walk 6 --- [LD41.P] Duplications with other complex rearrangements --PARENT--> [LD41] Duplications of the autosomes --PARENT--> [?] Chromosomal anomalies, excluding gene mutations Def: Any disease caused by alteration of the number or structure of chromosomes....
[ "[2F21.Y] Other specified benign keratinocytic acanthomas\n --PARENT--> [2F21] Benign keratinocytic acanthomas\n Def: A group of benign discrete epidermal proliferative disorders including seborrhoeic keratosis and clear cell acanthoma....\n --CHILD--> [2F21.0] Seborrhoeic keratosis\n Def: Seborrhoeic keratoses are very common benign neoplasms of epidermal keratinocytes which increase in prevalence and number with age. They are commonly multiple and are very variable in shape and colour...", "[2F21.Y] Other specified benign keratinocytic acanthomas\n --PARENT--> [2F21] Benign keratinocytic acanthomas\n Def: A group of benign discrete epidermal proliferative disorders including seborrhoeic keratosis and clear cell acanthoma....\n --CHILD--> [2F21.0] Seborrhoeic keratosis\n Def: Seborrhoeic keratoses are very common benign neoplasms of epidermal keratinocytes which increase in prevalence and number with age. They are commonly multiple and are very variable in shape and colour...", "[2F7Z] Neoplasms of uncertain behaviour of unspecified site\n --PARENT--> [?] Neoplasms of uncertain behaviour, except of lymphoid, haematopoietic, central nervous system or related tissues\n Def: A neoplasm except of lymphoid, haematopoietic, central nervous system or related tissues displaying morphologic, phenotypic, or genotypic characteristics that are clearly not benign but do not permit ...\n --CHILD--> [2F71] Neoplasms of uncertain behaviour of middle ear, respiratory or intrathoracic organs", "[2F7Z] Neoplasms of uncertain behaviour of unspecified site\n --PARENT--> [?] Neoplasms of uncertain behaviour, except of lymphoid, haematopoietic, central nervous system or related tissues\n Def: A neoplasm except of lymphoid, haematopoietic, central nervous system or related tissues displaying morphologic, phenotypic, or genotypic characteristics that are clearly not benign but do not permit ...\n --RELATED_TO--> [?] Pathological fracture in neoplastic disease of uncertain behaviour", "[LD41.P] Duplications with other complex rearrangements\n --PARENT--> [LD41] Duplications of the autosomes\n --CHILD--> [LD41.1] Duplications of chromosome 2", "[LD41.P] Duplications with other complex rearrangements\n --PARENT--> [LD41] Duplications of the autosomes\n --PARENT--> [?] Chromosomal anomalies, excluding gene mutations\n Def: Any disease caused by alteration of the number or structure of chromosomes...." ]
2F21.Y
Other specified benign keratinocytic acanthomas
[ { "from_icd11": "2F7Z", "icd10_code": "D482", "icd10_title": "Neoplasm of uncertain behavior of peripheral nerves and autonomic nervous system" }, { "from_icd11": "2F7Z", "icd10_code": "D37-D48", "icd10_title": "" }, { "from_icd11": "LD41.P", "icd10_code": "Q925", "icd10_title": "Duplications with other complex rearrangements" }, { "from_icd11": "QA03.Z", "icd10_code": "Z10", "icd10_title": "" }, { "from_icd11": "QA03.Z", "icd10_code": "Z108", "icd10_title": "" }, { "from_icd11": "QC10", "icd10_code": "Z5309", "icd10_title": "Procedure and treatment not carried out because of other contraindication" }, { "from_icd11": "QC10", "icd10_code": "Z530", "icd10_title": "Procedure and treatment not carried out because of contraindication" }, { "from_icd11": "QC04.5", "icd10_code": "Z2821", "icd10_title": "Immunization not carried out because of patient refusal" }, { "from_icd11": "QC04.5", "icd10_code": "Z282", "icd10_title": "Immunization not carried out because of patient decision for other and unspecified reason" }, { "from_icd11": "QC04.Z", "icd10_code": "Z283", "icd10_title": "Underimmunization status" }, { "from_icd11": "QC04.Z", "icd10_code": "Z2803", "icd10_title": "Immunization not carried out because of immune compromised state of patient" }, { "from_icd11": "QC04.Z", "icd10_code": "Z2809", "icd10_title": "Immunization not carried out because of other contraindication" }, { "from_icd11": "QC04.Z", "icd10_code": "Z2802", "icd10_title": "Immunization not carried out because of chronic illness or condition of patient" }, { "from_icd11": "QC04.Z", "icd10_code": "Z2882", "icd10_title": "Immunization not carried out because of caregiver refusal" }, { "from_icd11": "QC04.Z", "icd10_code": "Z2889", "icd10_title": "Immunization not carried out for other reason" } ]
D482
Neoplasm of uncertain behavior of peripheral nerves and autonomic nervous system
The diagnosis of systemic mastocytosis in our case report was established based on the presence of 1 major (the presence of mast cells in the bone marrow biopsy tissue) and 3 minor criteria (KIT-activating KIT point mutation at codon 816, CD25+ mast cells in bone marrow, and baseline serum tryptase concentration >20 ng/mL). Concomitant vertebral and cardiac impairment may be the consequence of the lesions associated with mastocytosis, which would explain the rapid evolution towards perforation of the mitral valve through the profibrotic pathways. Although it is the only case of systemic mastocytosis reported in the literature to date, which associates infective endocarditis caused by a pathogen rarely encountered in human pathology, we consider that it is important to include in the possible cardiovascular diseases associated with mastocytosis also infective endocarditis. The association of infective endocarditis with S. pseudoporcinus with pneumonia or pulmonary empyema , on aortic valve , associated with chronic obstructive pulmonary disease (COPD), mitral valve prolapses, and history of pulmonary embolism , in pregnant women was described, but never in the infective endocarditis-spondylodiscitis-mastocytosis triad. In terms of the limitations of our case report, they are related to the lack of etiological diagnosis of spondylodiscitis, the case being treated conservatively and not surgically.
4.152344
0.912598
sec[2]/p[2]
en
0.999997
37235295
https://doi.org/10.3390/tropicalmed8050247
[ "mastocytosis", "infective", "endocarditis", "associated", "valve", "pulmonary", "systemic", "presence", "mast", "cells" ]
[ { "code": "2A21.Z", "title": "Mastocytosis, unspecified" }, { "code": "2A21.Y", "title": "Other specified mastocytosis" }, { "code": "2A21.0Z", "title": "Systemic mastocytosis, unspecified" }, { "code": "2A21.1Z", "title": "Cutaneous mastocytosis, unspecified" }, { "code": "2A21.0Y", "title": "Other specified systemic mastocytosis" }, { "code": "1H0Z", "title": "Infection, unspecified" }, { "code": "1G40", "title": "Sepsis without septic shock" }, { "code": "FA10.Z", "title": "Direct infections of joint, unspecified" }, { "code": "1D9Z", "title": "Unspecified viral infection of unspecified site" }, { "code": "1A40.Z", "title": "Infectious gastroenteritis or colitis without specification of infectious agent" } ]
=== ICD-11 CODES FOUND === [2A21.Z] Mastocytosis, unspecified Also known as: Mastocytosis, unspecified | Mastocytosis | malignant mastocytoma | malignant mast cell tumours | malignant mastocytosis [2A21.Y] Other specified mastocytosis Also known as: Other specified mastocytosis [2A21.0Z] Systemic mastocytosis, unspecified Also known as: Systemic mastocytosis, unspecified | Systemic mastocytosis | SMCD - [systemic mast cell disease] | systemic tissue mast cell disease [2A21.1Z] Cutaneous mastocytosis, unspecified Also known as: Cutaneous mastocytosis, unspecified | Cutaneous mastocytosis [2A21.0Y] Other specified systemic mastocytosis Also known as: Other specified systemic mastocytosis | Indolent systemic mastocytosis | Isolated bone marrow mastocytosis | Smouldering systemic mastocytosis | Systemic mastocytosis with an associated clonal haematologic non-mast cell lineage disease [1H0Z] Infection, unspecified Also known as: Infection, unspecified | infection NOS | infectious disease NOS | infection unknown | infection process NOS [1G40] Sepsis without septic shock Definition: Sepsis is defined as a life-threatening organ dysfunction caused by a dysregulated host response to infection. Also known as: Sepsis without septic shock | sepsis without septic shock with known organism | Sepsis-associated hypotension | Unspecified sepsis | general septic intoxication Excludes: Septicaemia | Sepsis of fetus or newborn [FA10.Z] Direct infections of joint, unspecified Also known as: Direct infections of joint, unspecified | Direct infections of joint | septic arthritis | pyogenic arthritis | arthritis due to infection [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 [1A40.Z] Infectious gastroenteritis or colitis without specification of infectious agent Also known as: Infectious gastroenteritis or colitis without specification of infectious agent | Gastroenteritis or colitis without specification of infectious agent | diarrhoea and gastroenteritis of presumed infectious origin | diarrhoeal enteritis | GE - [gastroenteritis] === GRAPH WALKS === --- Walk 1 --- [2A21.Z] Mastocytosis, unspecified --PARENT--> [2A21] Mastocytosis Def: Mastocytosis is due to a clonal, neoplastic proliferation of mast cells that accumulate in one or more organ systems. Activating mutations of KIT are frequently found. It is characterised by the prese... --CHILD--> [2A21.0] Systemic mastocytosis Def: Systemic mastocytosis (SM) comprises a heterogeneous group of rare acquired and chronic haematological malignancies that are related to an abnormal proliferation of mast cells in tissue, including bon... --- Walk 2 --- [2A21.Z] Mastocytosis, unspecified --PARENT--> [2A21] Mastocytosis Def: Mastocytosis is due to a clonal, neoplastic proliferation of mast cells that accumulate in one or more organ systems. Activating mutations of KIT are frequently found. It is characterised by the prese... --CHILD--> [2A21.0] Systemic mastocytosis Def: Systemic mastocytosis (SM) comprises a heterogeneous group of rare acquired and chronic haematological malignancies that are related to an abnormal proliferation of mast cells in tissue, including bon... --- Walk 3 --- [2A21.Y] Other specified mastocytosis --PARENT--> [2A21] Mastocytosis Def: Mastocytosis is due to a clonal, neoplastic proliferation of mast cells that accumulate in one or more organ systems. Activating mutations of KIT are frequently found. It is characterised by the prese... --CHILD--> [2A21.2] Mast cell sarcoma Def: A rare entity characterised by localised but destructive growth of a tumour consisting of highly atypical, immature mast cells.... --- Walk 4 --- [2A21.Y] Other specified mastocytosis --PARENT--> [2A21] Mastocytosis Def: Mastocytosis is due to a clonal, neoplastic proliferation of mast cells that accumulate in one or more organ systems. Activating mutations of KIT are frequently found. It is characterised by the prese... --PARENT--> [?] Myeloproliferative neoplasms --- Walk 5 --- [2A21.0Z] Systemic mastocytosis, unspecified --PARENT--> [2A21.0] Systemic mastocytosis Def: Systemic mastocytosis (SM) comprises a heterogeneous group of rare acquired and chronic haematological malignancies that are related to an abnormal proliferation of mast cells in tissue, including bon... --CHILD--> [2A21.0Z] Systemic mastocytosis, unspecified --- Walk 6 --- [2A21.0Z] Systemic mastocytosis, unspecified --PARENT--> [2A21.0] Systemic mastocytosis Def: Systemic mastocytosis (SM) comprises a heterogeneous group of rare acquired and chronic haematological malignancies that are related to an abnormal proliferation of mast cells in tissue, including bon... --CHILD--> [2A21.0Y] Other specified systemic mastocytosis
[ "[2A21.Z] Mastocytosis, unspecified\n --PARENT--> [2A21] Mastocytosis\n Def: Mastocytosis is due to a clonal, neoplastic proliferation of mast cells that accumulate in one or more organ systems. Activating mutations of KIT are frequently found. It is characterised by the prese...\n --CHILD--> [2A21.0] Systemic mastocytosis\n Def: Systemic mastocytosis (SM) comprises a heterogeneous group of rare acquired and chronic haematological malignancies that are related to an abnormal proliferation of mast cells in tissue, including bon...", "[2A21.Z] Mastocytosis, unspecified\n --PARENT--> [2A21] Mastocytosis\n Def: Mastocytosis is due to a clonal, neoplastic proliferation of mast cells that accumulate in one or more organ systems. Activating mutations of KIT are frequently found. It is characterised by the prese...\n --CHILD--> [2A21.0] Systemic mastocytosis\n Def: Systemic mastocytosis (SM) comprises a heterogeneous group of rare acquired and chronic haematological malignancies that are related to an abnormal proliferation of mast cells in tissue, including bon...", "[2A21.Y] Other specified mastocytosis\n --PARENT--> [2A21] Mastocytosis\n Def: Mastocytosis is due to a clonal, neoplastic proliferation of mast cells that accumulate in one or more organ systems. Activating mutations of KIT are frequently found. It is characterised by the prese...\n --CHILD--> [2A21.2] Mast cell sarcoma\n Def: A rare entity characterised by localised but destructive growth of a tumour consisting of highly atypical, immature mast cells....", "[2A21.Y] Other specified mastocytosis\n --PARENT--> [2A21] Mastocytosis\n Def: Mastocytosis is due to a clonal, neoplastic proliferation of mast cells that accumulate in one or more organ systems. Activating mutations of KIT are frequently found. It is characterised by the prese...\n --PARENT--> [?] Myeloproliferative neoplasms", "[2A21.0Z] Systemic mastocytosis, unspecified\n --PARENT--> [2A21.0] Systemic mastocytosis\n Def: Systemic mastocytosis (SM) comprises a heterogeneous group of rare acquired and chronic haematological malignancies that are related to an abnormal proliferation of mast cells in tissue, including bon...\n --CHILD--> [2A21.0Z] Systemic mastocytosis, unspecified", "[2A21.0Z] Systemic mastocytosis, unspecified\n --PARENT--> [2A21.0] Systemic mastocytosis\n Def: Systemic mastocytosis (SM) comprises a heterogeneous group of rare acquired and chronic haematological malignancies that are related to an abnormal proliferation of mast cells in tissue, including bon...\n --CHILD--> [2A21.0Y] Other specified systemic mastocytosis" ]
2A21.Z
Mastocytosis, unspecified
[ { "from_icd11": "2A21.Z", "icd10_code": "C9621", "icd10_title": "Aggressive systemic mastocytosis" }, { "from_icd11": "2A21.Z", "icd10_code": "Q822", "icd10_title": "Congenital cutaneous mastocytosis" }, { "from_icd11": "2A21.Z", "icd10_code": "C962", "icd10_title": "Malignant mast cell neoplasm" }, { "from_icd11": "1H0Z", "icd10_code": "B999", "icd10_title": "Unspecified infectious disease" }, { "from_icd11": "1H0Z", "icd10_code": "A312", "icd10_title": "Disseminated mycobacterium avium-intracellulare complex (DMAC)" }, { "from_icd11": "1H0Z", "icd10_code": "B998", "icd10_title": "Other infectious disease" }, { "from_icd11": "1H0Z", "icd10_code": "A249", "icd10_title": "Melioidosis, unspecified" }, { "from_icd11": "1H0Z", "icd10_code": "R6511", "icd10_title": "Systemic inflammatory response syndrome (SIRS) of non-infectious origin with acute organ dysfunction" }, { "from_icd11": "1H0Z", "icd10_code": "R6510", "icd10_title": "Systemic inflammatory response syndrome (SIRS) of non-infectious origin without acute organ dysfunction" }, { "from_icd11": "1H0Z", "icd10_code": "A318", "icd10_title": "Other mycobacterial infections" }, { "from_icd11": "1H0Z", "icd10_code": "A319", "icd10_title": "Mycobacterial infection, unspecified" }, { "from_icd11": "1H0Z", "icd10_code": "B948", "icd10_title": "Sequelae of other specified infectious and parasitic diseases" }, { "from_icd11": "1H0Z", "icd10_code": "B949", "icd10_title": "Sequelae of unspecified infectious and parasitic disease" }, { "from_icd11": "1H0Z", "icd10_code": "K77", "icd10_title": "Liver disorders in diseases classified elsewhere" }, { "from_icd11": "1H0Z", "icd10_code": "N771", "icd10_title": "Vaginitis, vulvitis and vulvovaginitis in diseases classified elsewhere" } ]
C9621
Aggressive systemic mastocytosis
Plaza, et al. conducted an extensive study over a 30-year period of 118 patients diagnosed with metastatic soft tissues stemming from a wide variety of primary tumor sites . Out of all of these cases, only 1 patient, a 54-year-old man was determined to have testicular cancer metastasis to a soft tissue mass in his thigh. Similarly, Bilici, et al. published a case report of a 41-year-old patient with a history of a left radical orchiectomy and subsequent lesions in his liver and brain who presented with a lump, but no pain, in his left thigh 7 years after the diagnosis of testicular cancer . Magnetic resonance imaging (MRI) and biopsy determined a soft tissue malignant mass, which had metastasized from primary testicular cancer. Excision of the tumor eliminated his symptoms with no recurrence during 10-months’ follow-up. Finally, Degirmencioglu, et al, described a 62-year-old patient with a history of a right radical orchiectomy and lymph node resection who declined chemotherapy, and subsequently presented with pain, loss of motion, and swelling in his right leg 20 months’ later . Positron emission tomography (PET and/or CT) revealed a large hypermetabolic lesion into both the muscular soft tissue and bone, and a biopsy confirmed the diagnosis of metastasis from the earlier testicular malignancy. Here we report a case of non–seminomatous germ cell testicular cancer metastasis to iliopsoas muscle.
4.082031
0.87207
sec[0]/p[3]
en
0.999996
34007386
https://doi.org/10.1016/j.radcr.2021.04.004
[ "testicular", "soft", "cancer", "metastasis", "tissue", "tumor", "determined", "thigh", "radical", "orchiectomy" ]
[ { "code": "GB0Y&XA4947", "title": "Disease or disorder of testis, unspecified" }, { "code": "GB02.1&XA4947", "title": "Inflammation of testis" }, { "code": "LB51", "title": "Anorchia or microorchidia" }, { "code": "GB03", "title": "Atrophy of testis" }, { "code": "2F97&XA4947", "title": "Neoplasms of unknown behaviour of testis" }, { "code": "FB6Z", "title": "Soft tissue disorders, unspecified" }, { "code": "FB56.6", "title": "Other specified soft tissue disorders" }, { "code": "GB61.Z", "title": "Chronic kidney disease, stage unspecified" }, { "code": "FB56.1", "title": "Residual foreign body in soft tissue" }, { "code": "FB52", "title": "Soft tissue disorders in diseases classified elsewhere" } ]
=== ICD-11 CODES FOUND === [LB51] Anorchia or microorchidia Definition: A disorder affecting males, caused by an abnormality occurring in sex development during the antenatal period. This disorder is characterised by individuals who are born with absence of the testes, or with testes that are deficient in size and function. Confirmation is by physical examination, identification of low testosterone levels but elevated follicle stimulating hormone and luteinizing hormone levels in a blood sample, or imaging. Also known as: Anorchia or microorchidia | Absence or aplasia of testis, unilateral | congenital absence of testis, unilateral | congenital absent testicle | congenital absence of testis [GB03] Atrophy of testis Definition: A condition of the testis, caused by apoptosis of the cells due to diminished cellular proliferation, decreased cellular volume, decreased function, ischemia, malnutrition, disease, infection, mutation, or hormonal changes. This condition is characterised by a partial or complete decrease in size and function of the testis tissue. Also known as: Atrophy of testis | atrophic testicle | atrophy of testicle | testicular atrophy [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 [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 [FB56.1] Residual foreign body in soft tissue Also known as: Residual foreign body in soft tissue | residual foreign body in soft tissue, site unspecified | foreign body in soft tissue | Residual foreign body in soft tissue, multiple sites | Residual foreign body in soft tissue, shoulder region Excludes: Foreign body granuloma of skin | Foreign body granuloma of soft tissue, not elsewhere classified [FB52] Soft tissue disorders in diseases classified elsewhere Definition: This is a group of disorders affecting tissues that connect, support, or surround other structures and organs of the body, not being bone and occur in diseases classified elsewhere. Also known as: Soft tissue disorders in diseases classified elsewhere === GRAPH WALKS === --- Walk 1 --- [LB51] Anorchia or microorchidia Def: A disorder affecting males, caused by an abnormality occurring in sex development during the antenatal period. This disorder is characterised by individuals who are born with absence of the testes, or... --RELATED_TO--> [?] Testicular agenesis Def: A rare 46,XY disorder of gonadal development characterized by congenital complete absence of testicular tissue in an individual with an otherwise male phenotype and normal karyotype. In addition, a sm... --PARENT--> [?] 46,XY disorders of sex development due to a defect in testicular development --- Walk 2 --- [LB51] Anorchia or microorchidia Def: A disorder affecting males, caused by an abnormality occurring in sex development during the antenatal period. This disorder is characterised by individuals who are born with absence of the testes, or... --RELATED_TO--> [?] Testicular agenesis Def: A rare 46,XY disorder of gonadal development characterized by congenital complete absence of testicular tissue in an individual with an otherwise male phenotype and normal karyotype. In addition, a sm... --PARENT--> [?] 46,XY disorders of sex development due to a defect in testicular development --- Walk 3 --- [GB03] Atrophy of testis Def: A condition of the testis, caused by apoptosis of the cells due to diminished cellular proliferation, decreased cellular volume, decreased function, ischemia, malnutrition, disease, infection, mutatio... --PARENT--> [?] Diseases of the male genital system Def: Any disease characterised by pathological changes to the male genital system.... --CHILD--> [GB00] Hydrocele or spermatocele Def: A condition characterised by an accumulation of serous fluid in the tunica vaginalis testis or along the spermatic cord, and cystic swelling containing fluid and dead spermatozoa of the testicular epi... --- Walk 4 --- [GB03] Atrophy of testis Def: A condition of the testis, caused by apoptosis of the cells due to diminished cellular proliferation, decreased cellular volume, decreased function, ischemia, malnutrition, disease, infection, mutatio... --PARENT--> [?] Diseases of the male genital system Def: Any disease characterised by pathological changes to the male genital system.... --CHILD--> [GB00] Hydrocele or spermatocele Def: A condition characterised by an accumulation of serous fluid in the tunica vaginalis testis or along the spermatic cord, and cystic swelling containing fluid and dead spermatozoa of the testicular epi...
[ "[LB51] Anorchia or microorchidia\n Def: A disorder affecting males, caused by an abnormality occurring in sex development during the antenatal period. This disorder is characterised by individuals who are born with absence of the testes, or...\n --RELATED_TO--> [?] Testicular agenesis\n Def: A rare 46,XY disorder of gonadal development characterized by congenital complete absence of testicular tissue in an individual with an otherwise male phenotype and normal karyotype. In addition, a sm...\n --PARENT--> [?] 46,XY disorders of sex development due to a defect in testicular development", "[LB51] Anorchia or microorchidia\n Def: A disorder affecting males, caused by an abnormality occurring in sex development during the antenatal period. This disorder is characterised by individuals who are born with absence of the testes, or...\n --RELATED_TO--> [?] Testicular agenesis\n Def: A rare 46,XY disorder of gonadal development characterized by congenital complete absence of testicular tissue in an individual with an otherwise male phenotype and normal karyotype. In addition, a sm...\n --PARENT--> [?] 46,XY disorders of sex development due to a defect in testicular development", "[GB03] Atrophy of testis\n Def: A condition of the testis, caused by apoptosis of the cells due to diminished cellular proliferation, decreased cellular volume, decreased function, ischemia, malnutrition, disease, infection, mutatio...\n --PARENT--> [?] Diseases of the male genital system\n Def: Any disease characterised by pathological changes to the male genital system....\n --CHILD--> [GB00] Hydrocele or spermatocele\n Def: A condition characterised by an accumulation of serous fluid in the tunica vaginalis testis or along the spermatic cord, and cystic swelling containing fluid and dead spermatozoa of the testicular epi...", "[GB03] Atrophy of testis\n Def: A condition of the testis, caused by apoptosis of the cells due to diminished cellular proliferation, decreased cellular volume, decreased function, ischemia, malnutrition, disease, infection, mutatio...\n --PARENT--> [?] Diseases of the male genital system\n Def: Any disease characterised by pathological changes to the male genital system....\n --CHILD--> [GB00] Hydrocele or spermatocele\n Def: A condition characterised by an accumulation of serous fluid in the tunica vaginalis testis or along the spermatic cord, and cystic swelling containing fluid and dead spermatozoa of the testicular epi..." ]
GB0Y&XA4947
Disease or disorder of testis, unspecified
[ { "from_icd11": "LB51", "icd10_code": "Q550", "icd10_title": "Absence and aplasia of testis" }, { "from_icd11": "LB51", "icd10_code": "Q55", "icd10_title": "Other congenital malformations of male genital organs" }, { "from_icd11": "GB03", "icd10_code": "N503", "icd10_title": "Cyst of epididymis" }, { "from_icd11": "GB03", "icd10_code": "N500", "icd10_title": "Atrophy of testis" }, { "from_icd11": "GB03", "icd10_code": "N50", "icd10_title": "Other and unspecified disorders of male genital organs" }, { "from_icd11": "2F97&XA4947", "icd10_code": "D401", "icd10_title": "Neoplasm of uncertain behavior of testis" }, { "from_icd11": "FB6Z", "icd10_code": "M60-M79", "icd10_title": "" }, { "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": "FB56.1", "icd10_code": "M795", "icd10_title": "Residual foreign body in soft tissue" } ]
Q550
Absence and aplasia of testis
A 71-year-old man with no medical history was admitted to the emergency department of a peripheral hospital because of shortness of breath. About eight days before, he tested positive for SARS-CoV−2. The chest scan revealed extensive bilateral ground glass opacities. Oxygen via nasal cannula was started, but acute respiratory failure developed after one day, requiring ventilation with HCPAP. After five days since hospital admission, following repeated unsuccessful attempts at prone positioning, the clinical condition suddenly deteriorated, and he was moved to our hospital for intubation and ICU admission due to acute respiratory distress syndrome related to SARS-CoV-2 pneumonia. At admission, volume-controlled ventilation was started with cycles of prone positioning. IV dexamethasone and an empiric antibiotic course with ceftriaxone were started. A rectal swab was positive for DTR-AB. Six days after admission, oxygen saturation levels improved, and respiratory weaning from mechanical ventilation was started. However, in the eight days of ICU, he developed fever, neutrophil leukocytosis and a new onset of respiratory failure requiring new intubation. Blood culture results were positive for DTR-AB, E. faecalis and E. faecium, and a bronchoalveolar lavage (BAL) culture was positive for DTR-AB > 100,000 CFU/mL. He eventually required norepinephrine to maintain hemodynamic stability and CVVH for AKI.
3.882813
0.981934
sec[1]/sec[1]/p[0]
en
0.999997
PMC9774561
https://doi.org/10.3390/antibiotics11121830
[ "respiratory", "ventilation", "eight", "sars", "oxygen", "failure", "requiring", "prone", "positioning", "intubation" ]
[ { "code": "CB7Z", "title": "Diseases of the respiratory system, unspecified" }, { "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": "MD11.7", "title": "Hyperventilation" }, { "code": "PK81.0", "title": "Ventilation associated with injury or harm in therapeutic use" }, { "code": "QB41", "title": "Dependence on respirator" }, { "code": "CA70.7", "title": "Air conditioner or humidifier lung" }, { "code": "1D65", "title": "Severe acute respiratory syndrome" } ]
=== 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 [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 [MD11.7] Hyperventilation Definition: Hyperventilation refers to an increase in the rate of alveolar ventilation that is excessive for the rate of metabolic carbon dioxide production, resulting in a decrease in arterial PCO2 to below the normal range of 37 to 43 mm Hg. Hyperventilation should be distinguished from tachypnoea, an increase in respiratory frequency, and from hyperpnea, an increase in minute volume of ventilation. Also known as: Hyperventilation | hyperventilating | overbreathing | HV - [hyperventilation] | increased respiratory rate [PK81.0] Ventilation associated with injury or harm in therapeutic use Also known as: Ventilation associated with injury or harm in therapeutic use | complication during or following ventilation | Ventilator associated pneumonia | VAP - [ventilator associated pneumonia] | respirator associated pneumonia Excludes: Circumstances associated with a surgical or other medical procedure influencing the episode of care, without injury or harm [QB41] Dependence on respirator Also known as: Dependence on respirator | dependence on iron lung | dependence on respiratory ventilator [CA70.7] Air conditioner or humidifier lung Definition: A form of the sick building syndrome caused by organisms that contaminate humidifiers and the piping of air conditioner ducts. The air conditioner blows cold air containing spores of the organisms throughout the building. Also known as: Air conditioner or humidifier lung | air conditioner lung | air humidifier pneumonitis | humidifier lung | sauna takers lung [1D65] Severe acute respiratory syndrome Definition: A disease of the respiratory system, caused by an infection with coronavirus. This disease is characterised by fever, headache, cough, myalgia, tachycardia, or diarrhoea. This disease may also lead to pneumonia. Transmission is by direct contact, inhalation of infected respiratory secretions, or airborne transmission. Confirmation is by identification of coronavirus in a blood, stool, respiratory secretions, or body tissue sample. Also known as: Severe acute respiratory syndrome | SARS - [severe acute respiratory syndrome] Excludes: COVID-19, virus identified | COVID-19, virus not identified === 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 --RELATED_TO--> [?] Pulmonary heart disease or diseases of pulmonary circulation --- Walk 3 --- [CB41] Respiratory failure Def: 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.... --CHILD--> [CB41.0] Acute respiratory failure Def: Respiratory failure can be acute (short term) or chronic (ongoing), using time as the main parameter. In acute respiratory failure hypoxemia occurs over a period of hours to days (less than 7 days), a... --PARENT--> [CB41] Respiratory failure Def: 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.... --- Walk 4 --- [CB41] Respiratory failure Def: 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.... --EXCLUDES--> [?] Respiratory arrest Def: Arrest of spontaneous breathing.... --PARENT--> [?] Symptoms or signs involving the respiratory system --- Walk 5 --- [CB41.2Z] Respiratory failure, unspecified --PARENT--> [CB41.2] Respiratory failure, unspecified as acute or chronic Def: This is inadequate gas exchange by the respiratory system, with the result that levels of arterial oxygen, carbon dioxide or both cannot be maintained within their normal ranges, unspecified as acute ... --CHILD--> [CB41.21] Respiratory failure, unspecified, Type II Def: Type 2 respiratory failure is caused by inadequate ventilation; both oxygen and carbon dioxide are affected. Defined as the build up of carbon dioxide levels (PaCO2) that has been generated by the bod... --- Walk 6 --- [CB41.2Z] Respiratory failure, unspecified --PARENT--> [CB41.2] Respiratory failure, unspecified as acute or chronic Def: This is inadequate gas exchange by the respiratory system, with the result that levels of arterial oxygen, carbon dioxide or both cannot be maintained within their normal ranges, unspecified as acute ... --CHILD--> [CB41.20] Respiratory failure, unspecified, Type I Def: This is when the PaCO2 may be normal or low. It is typically caused by a ventilation/perfusion (V/Q) mismatch; the volume of air flowing in and out of the lungs is not matched with the flow of blood t...
[ "[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 --RELATED_TO--> [?] Pulmonary heart disease or diseases of pulmonary circulation", "[CB41] Respiratory failure\n Def: 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....\n --CHILD--> [CB41.0] Acute respiratory failure\n Def: Respiratory failure can be acute (short term) or chronic (ongoing), using time as the main parameter. In acute respiratory failure hypoxemia occurs over a period of hours to days (less than 7 days), a...\n --PARENT--> [CB41] Respiratory failure\n Def: 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....", "[CB41] Respiratory failure\n Def: 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....\n --EXCLUDES--> [?] Respiratory arrest\n Def: Arrest of spontaneous breathing....\n --PARENT--> [?] Symptoms or signs involving the respiratory system", "[CB41.2Z] Respiratory failure, unspecified\n --PARENT--> [CB41.2] Respiratory failure, unspecified as acute or chronic\n Def: This is inadequate gas exchange by the respiratory system, with the result that levels of arterial oxygen, carbon dioxide or both cannot be maintained within their normal ranges, unspecified as acute ...\n --CHILD--> [CB41.21] Respiratory failure, unspecified, Type II\n Def: Type 2 respiratory failure is caused by inadequate ventilation; both oxygen and carbon dioxide are affected. Defined as the build up of carbon dioxide levels (PaCO2) that has been generated by the bod...", "[CB41.2Z] Respiratory failure, unspecified\n --PARENT--> [CB41.2] Respiratory failure, unspecified as acute or chronic\n Def: This is inadequate gas exchange by the respiratory system, with the result that levels of arterial oxygen, carbon dioxide or both cannot be maintained within their normal ranges, unspecified as acute ...\n --CHILD--> [CB41.20] Respiratory failure, unspecified, Type I\n Def: This is when the PaCO2 may be normal or low. It is typically caused by a ventilation/perfusion (V/Q) mismatch; the volume of air flowing in and out of the lungs is not matched with the flow of blood t..." ]
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": "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" }, { "from_icd11": "CB41", "icd10_code": "J96", "icd10_title": "Respiratory failure, not elsewhere classified" }, { "from_icd11": "CB41.2Z", "icd10_code": "J9691", "icd10_title": "Respiratory failure, unspecified with hypoxia" }, { "from_icd11": "CB41.2Z", "icd10_code": "J9690", "icd10_title": "Respiratory failure, unspecified, unspecified whether with hypoxia or hypercapnia" }, { "from_icd11": "CB41.2Z", "icd10_code": "J9692", "icd10_title": "Respiratory failure, unspecified with hypercapnia" }, { "from_icd11": "CB41.2Z", "icd10_code": "J9621", "icd10_title": "Acute and chronic respiratory failure with hypoxia" }, { "from_icd11": "CB41.2Z", "icd10_code": "J969", "icd10_title": "Respiratory failure, unspecified" }, { "from_icd11": "MD11.7", "icd10_code": "R064", "icd10_title": "Hyperventilation" }, { "from_icd11": "QB41", "icd10_code": "Z9911", "icd10_title": "Dependence on respirator [ventilator] status" }, { "from_icd11": "QB41", "icd10_code": "Z991", "icd10_title": "Dependence on respirator" }, { "from_icd11": "CA70.7", "icd10_code": "J677", "icd10_title": "Air conditioner and humidifier lung" } ]
J989
Respiratory disorder, unspecified