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An 80-year-old woman with limited mobility was sent to the emergency department by a lathe with right hip pain after squatting while using the toilet. The patient was admitted to the hospital 14 days ago due to a right femoral neck fracture (Garden type III). We performed her a bipolar hip hemiarthroplast using a posterior later surgical approach . She could walk with the help of a walker after surgery. She was discharged 9 days after surgery. The Harris score was 90. The patient was accompanied by mild Alzheimer's disease and no history of the neuromuscular system. She did not listen to the doctor's advice and went to the bathroom to squat the toilet 11 days following her hemiarthroplasty causing significant pain and an inability to weight bear on the right side. On examination of the patient, it was noted that the right lower limb was shortened and externally rotated, raising concern for a dislocation. A radiograph of the pelvis showed a dislocation of the hemiarthroplasty with proximal migration . We judged that the poor posture of hip flexion and adduction during squatting led to the occurrence of posterior hip dislocation. Fig. 1 Anteroposterior radiograph of the right hip demonstrating a satisfactory hip hemiarthroplasty subsequent to a subcapital neck of femur fracture. Fig. 1 Fig. 2 Anteroposterior radiograph of the right hipdemonstrating a dislocation of right hip hemiarthroplasty. Fig. 2
3.636719
0.986328
sec[1]/p[0]
en
0.999999
32693236
https://doi.org/10.1016/j.ijscr.2020.06.071
[ "hemiarthroplasty", "dislocation", "radiograph", "pain", "squatting", "using", "toilet", "neck", "fracture", "that" ]
[ { "code": "NE83.0", "title": "Destruction or cartilage wear of joint with hemiarthroplasty" }, { "code": "ND56.3", "title": "Dislocation or strain or sprain of unspecified body region" }, { "code": "ND33", "title": "Dislocations, strains or sprains involving multiple body regions" }, { "code": "FA34.2", "title": "Recurrent instability of joint" }, { "code": "NB53.1", "title": "Dislocation of lumbar vertebra" }, { "code": "CA0D", "title": "Deviated nasal septum" }, { "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 === [NE83.0] Destruction or cartilage wear of joint with hemiarthroplasty Also known as: Destruction or cartilage wear of joint with hemiarthroplasty [ND56.3] Dislocation or strain or sprain of unspecified body region Also known as: Dislocation or strain or sprain of unspecified body region | subluxation NOS | Dislocation or subluxation | dislocation NOS | Traumatic subluxation of joint Excludes: multiple dislocations, sprains and strains NOS [ND33] Dislocations, strains or sprains involving multiple body regions Also known as: Dislocations, strains or sprains involving multiple body regions | Dislocations, strains or sprains involving head with neck | Dislocations, sprains and strains of sites classifiable as head or neck level | Multiple dislocations of head and neck | Multiple sprains of head and neck [FA34.2] Recurrent instability of joint Also known as: Recurrent instability of joint | recurrent dislocation and subluxation of joint | recrudescent dislocation | recurrent dislocation | Brill-Zinsser dislocation Excludes: vertebral subluxation | Recurrent instability of patella [NB53.1] Dislocation of lumbar vertebra Also known as: Dislocation of lumbar vertebra | dislocation of joint of lumbar spine | traumatic dislocation of joint of lumbar vertebra | acute traumatic lumbar spondylolisthesis | lumbar dislocation [CA0D] Deviated nasal septum Also known as: Deviated nasal septum | deflected nasal septum | deflected septum | nasal septum deviation | crooked nasal septum [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 --- [NE83.0] Destruction or cartilage wear of joint with hemiarthroplasty --PARENT--> [NE83] Injury or harm arising from other device, implant or graft, not elsewhere classified --CHILD--> [NE83.1] Infection arising from device, implant or graft, not elsewhere classified --- Walk 2 --- [NE83.0] Destruction or cartilage wear of joint with hemiarthroplasty --PARENT--> [NE83] Injury or harm arising from other device, implant or graft, not elsewhere classified --RELATED_TO--> [?] Cardiac conduit failure Def: Lack of preservation of function of a cardiac conduit, that may result in the necessity for revision or replacement... --- Walk 3 --- [ND56.3] Dislocation or strain or sprain of unspecified body region --EXCLUDES--> [?] Dislocations, strains or sprains involving multiple body regions --CHILD--> [?] Dislocations, strains or sprains involving thorax with lower back or pelvis --- Walk 4 --- [ND56.3] Dislocation or strain or sprain of unspecified body region --EXCLUDES--> [?] Dislocations, strains or sprains involving multiple body regions --CHILD--> [?] Dislocations, strains or sprains involving multiple regions of arm --- Walk 5 --- [ND33] Dislocations, strains or sprains involving multiple body regions --PARENT--> [?] Injuries involving multiple body regions --EXCLUDES--> [?] Frostbite Def: Frostbite is injury from ice formation within tissues resulting from contact with cold air, liquids or metals. It is most commonly due to excessive exposure of skin to sub-zero environmental temperatu... --- Walk 6 --- [ND33] Dislocations, strains or sprains involving multiple body regions --PARENT--> [?] Injuries involving multiple body regions --EXCLUDES--> [?] Burns Def: A burn is an injury to the tissues caused by a pathological flux of energy which causes cellular destruction and irreversible denaturation of proteins and is primarily caused by thermal or other acute...
[ "[NE83.0] Destruction or cartilage wear of joint with hemiarthroplasty\n --PARENT--> [NE83] Injury or harm arising from other device, implant or graft, not elsewhere classified\n --CHILD--> [NE83.1] Infection arising from device, implant or graft, not elsewhere classified", "[NE83.0] Destruction or cartilage wear of joint with hemiarthroplasty\n --PARENT--> [NE83] Injury or harm arising from other device, implant or graft, not elsewhere classified\n --RELATED_TO--> [?] Cardiac conduit failure\n Def: Lack of preservation of function of a cardiac conduit, that may result in the necessity for revision or replacement...", "[ND56.3] Dislocation or strain or sprain of unspecified body region\n --EXCLUDES--> [?] Dislocations, strains or sprains involving multiple body regions\n --CHILD--> [?] Dislocations, strains or sprains involving thorax with lower back or pelvis", "[ND56.3] Dislocation or strain or sprain of unspecified body region\n --EXCLUDES--> [?] Dislocations, strains or sprains involving multiple body regions\n --CHILD--> [?] Dislocations, strains or sprains involving multiple regions of arm", "[ND33] Dislocations, strains or sprains involving multiple body regions\n --PARENT--> [?] Injuries involving multiple body regions\n --EXCLUDES--> [?] Frostbite\n Def: Frostbite is injury from ice formation within tissues resulting from contact with cold air, liquids or metals. It is most commonly due to excessive exposure of skin to sub-zero environmental temperatu...", "[ND33] Dislocations, strains or sprains involving multiple body regions\n --PARENT--> [?] Injuries involving multiple body regions\n --EXCLUDES--> [?] Burns\n Def: A burn is an injury to the tissues caused by a pathological flux of energy which causes cellular destruction and irreversible denaturation of proteins and is primarily caused by thermal or other acute..." ]
NE83.0
Destruction or cartilage wear of joint with hemiarthroplasty
[ { "from_icd11": "ND56.3", "icd10_code": "T143", "icd10_title": "" }, { "from_icd11": "ND33", "icd10_code": "T03", "icd10_title": "" }, { "from_icd11": "ND33", "icd10_code": "T030", "icd10_title": "" }, { "from_icd11": "ND33", "icd10_code": "T031", "icd10_title": "" }, { "from_icd11": "ND33", "icd10_code": "T032", "icd10_title": "" }, { "from_icd11": "ND33", "icd10_code": "T033", "icd10_title": "" }, { "from_icd11": "ND33", "icd10_code": "T034", "icd10_title": "" }, { "from_icd11": "ND33", "icd10_code": "T038", "icd10_title": "" }, { "from_icd11": "ND33", "icd10_code": "T039", "icd10_title": "" }, { "from_icd11": "FA34.2", "icd10_code": "M24452", "icd10_title": "Recurrent dislocation, left hip" }, { "from_icd11": "FA34.2", "icd10_code": "M24451", "icd10_title": "Recurrent dislocation, right hip" }, { "from_icd11": "FA34.2", "icd10_code": "M24475", "icd10_title": "Recurrent dislocation, left foot" }, { "from_icd11": "FA34.2", "icd10_code": "M24411", "icd10_title": "Recurrent dislocation, right shoulder" }, { "from_icd11": "FA34.2", "icd10_code": "M24412", "icd10_title": "Recurrent dislocation, left shoulder" }, { "from_icd11": "FA34.2", "icd10_code": "M24422", "icd10_title": "Recurrent dislocation, left elbow" } ]
T143
A 33-year-old woman presented to the ED with a severe, right-sided, throbbing headache for the last five days, which was associated with vomiting and photophobia. She denied any trauma or manipulation except for her daily stretches. She had a medical history of catamenial migraine without aura, mostly pulsatile, and localized to the frontotemporal region. She reported that her presenting attack had been preceded by a sudden onset of visual symptoms in the left visual field and characterized by several scotomas, zig-zag lines, and dark holes. Moreover, she rated her pain intensity as 7 out of 10 and described an unusual location in an occipital region with mild right neck tenderness. She reported some response to acetazolamide with analgesics and triptans in severe attacks. MRI brain and MR venography were unremarkable; hence, she was treated as status migrainosus with intravenous (IV) valproic acid and metoclopramide with partial improvement. Three days later, she presented again to the ED with frequent vomiting, hiccups, dizziness, dysarthria, and blurring of vision. Neurological examination revealed the loss of sensation over the right side of the face, right upper limb ataxia, nystagmus with right eye ptosis, and constricted pupil (Horner syndrome). A new MRI of the brain showed right lateral medullary infarction , and MRA showed focal stenosis within V4 segments of the right vertebral artery .
3.914063
0.984375
sec[1]/p[5]
en
0.999998
32802618
https://doi.org/10.7759/cureus.9183
[ "vomiting", "region", "visual", "brain", "sided", "throbbing", "headache", "five", "which", "associated" ]
[ { "code": "MD90.1", "title": "Vomiting" }, { "code": "DD90.4", "title": "Functional nausea or vomiting" }, { "code": "ME24.A5", "title": "Haematemesis" }, { "code": "1A23", "title": "Enteritis due to Norovirus" }, { "code": "JA60.Z", "title": "Excessive vomiting in pregnancy, unspecified" }, { "code": "ND56.0", "title": "Superficial injury of unspecified body region" }, { "code": "ND56.Z", "title": "Unspecified injury to unspecified part of trunk, limb or body region" }, { "code": "CA44", "title": "Pyothorax" }, { "code": "FB3Z", "title": "Disorders of muscles, unspecified" }, { "code": "ND56.8", "title": "Traumatic amputation of unspecified body region" } ]
=== ICD-11 CODES FOUND === [MD90.1] Vomiting Also known as: Vomiting | emesis | hyperemesis | retching | Vomiting of faecal matter [DD90.4] Functional nausea or vomiting Definition: Functional nausea and vomiting is a disorder having no structural abnormalities for nausea and vomiting. Also known as: Functional nausea or vomiting | Chronic nausea vomiting syndrome | CNVS- [Chronic nausea vomiting syndrome] | Functional vomiting | Cannabinoid hyperemesis syndrome Excludes: Nausea or vomiting NOS [ME24.A5] Haematemesis Definition: Vomiting of blood that is either fresh bright red, or older "coffee-ground" in character. Vomiting blood is a regurgitation of blood through the upper gastrointestinal tract and it generally indicates bleeding of the upper gastrointestinal tract. Also known as: Haematemesis | vomiting blood | blood in vomit [1A23] Enteritis due to Norovirus Definition: A disease of the gastrointestinal tract, caused by an infection with norovirus. This disease is characterised by acute onset of vomiting, non-haemorrhagic diarrhoea, and abdominal pain. Transmission is by ingestion of contaminated food or water, direct contact, or through fomites. Confirmation is by identification of norovirus. Also known as: Enteritis due to Norovirus | acute gastroenteropathy due to Norwalk agent | viral gastroenteritis due to Norwalk agent | winter vomiting | epidemic winter vomiting disease [JA60.Z] Excessive vomiting in pregnancy, unspecified Also known as: Excessive vomiting in pregnancy, unspecified | Excessive vomiting in pregnancy | Vomiting of or complicating pregnancy [ND56.0] Superficial injury of unspecified body region Also known as: Superficial injury of unspecified body region | superficial injury of limb NOS | Superficial injury NOS | scratch NOS | Cutaneous wounds, injuries or scars Excludes: multiple superficial injuries NOS [ND56.Z] Unspecified injury to unspecified part of trunk, limb or body region Also known as: Unspecified injury to unspecified part of trunk, limb or body region | Injury of unspecified body region | injury NOS | trauma NOS | traumatic injury NOS [CA44] Pyothorax Definition: Suppurative inflammation of the pleural space, typically due to acute bacterial infection. It can occur as a complication of pneumonia, thoracotomy, abscesses (lung, hepatic, or subdiaphragmatic), or penetrating trauma with a secondary infection. Also known as: Pyothorax | empyema | pyopneumothorax | Pyothorax with fistula | empyema with fistula Includes: empyema | pyopneumothorax Excludes: due to tuberculosis [FB3Z] Disorders of muscles, unspecified Also known as: Disorders of muscles, unspecified | disorder of muscle, unspecified | muscle disease | muscular disease | muscular disorder [ND56.8] Traumatic amputation of unspecified body region Also known as: Traumatic amputation of unspecified body region | avulsion NOS | Traumatic amputation NOS | traumatic avulsion NOS | traumatic extremity loss Excludes: multiple: crushing injuries NOS | multiple traumatic amputations NOS === GRAPH WALKS === --- Walk 1 --- [MD90.1] Vomiting --RELATED_TO--> [?] Excessive vomiting in pregnancy --CHILD--> [?] Mild hyperemesis gravidarum Def: Vomiting occurring during pregnancy responsive to dietary modification and antiemetic treatment... --- Walk 2 --- [MD90.1] Vomiting --RELATED_TO--> [?] Vomiting in newborn Def: A paediatric condition characterised by the forceful expulsion of the contents of the stomach through the mouth and sometimes the nose of a newborn.... --PARENT--> [?] Certain disorders originating in the perinatal period Def: A group of any other paediatric conditions that occur during the period of time around childbirth, especially the five months before and one month after birth.... --- Walk 3 --- [DD90.4] Functional nausea or vomiting Def: Functional nausea and vomiting is a disorder having no structural abnormalities for nausea and vomiting.... --EXCLUDES--> [?] Nausea or vomiting Def: Nausea is the feeling of having an urge to vomit. Vomiting is forcing the contents of the stomach up through the oesophagus and out of the mouth.... --PARENT--> [?] Symptoms related to the upper gastrointestinal tract Def: Clinical symptoms presumed to be arising from disorders/diseases of upper GI tract.... --- Walk 4 --- [DD90.4] Functional nausea or vomiting Def: Functional nausea and vomiting is a disorder having no structural abnormalities for nausea and vomiting.... --RELATED_TO--> [?] Cyclic vomiting syndrome Def: Recurrent episodic attacks, usually stereotypical in the individual patient, of vomiting and intense nausea. Attacks are associated with pallor and lethargy. There is complete resolution of symptoms b... --PARENT--> [?] Functional nausea or vomiting Def: Functional nausea and vomiting is a disorder having no structural abnormalities for nausea and vomiting.... --- Walk 5 --- [ME24.A5] Haematemesis Def: Vomiting of blood that is either fresh bright red, or older "coffee-ground" in character. Vomiting blood is a regurgitation of blood through the upper gastrointestinal tract and it generally indicates... --RELATED_TO--> [?] Neonatal haematemesis or melaena due to swallowed maternal blood Def: A less serious, self-limiting case of haematemesis and melena which can occur in newborns two to three days after delivery, due to swallowed maternal blood.... --PARENT--> [?] Digestive system disorders of fetus or newborn --- Walk 6 --- [ME24.A5] Haematemesis Def: Vomiting of blood that is either fresh bright red, or older "coffee-ground" in character. Vomiting blood is a regurgitation of blood through the upper gastrointestinal tract and it generally indicates... --RELATED_TO--> [?] Neonatal haematemesis or melaena due to swallowed maternal blood Def: A less serious, self-limiting case of haematemesis and melena which can occur in newborns two to three days after delivery, due to swallowed maternal blood.... --PARENT--> [?] Haematemesis Def: Vomiting of blood that is either fresh bright red, or older "coffee-ground" in character. Vomiting blood is a regurgitation of blood through the upper gastrointestinal tract and it generally indicates...
[ "[MD90.1] Vomiting\n --RELATED_TO--> [?] Excessive vomiting in pregnancy\n --CHILD--> [?] Mild hyperemesis gravidarum\n Def: Vomiting occurring during pregnancy responsive to dietary modification and antiemetic treatment...", "[MD90.1] Vomiting\n --RELATED_TO--> [?] Vomiting in newborn\n Def: A paediatric condition characterised by the forceful expulsion of the contents of the stomach through the mouth and sometimes the nose of a newborn....\n --PARENT--> [?] Certain disorders originating in the perinatal period\n Def: A group of any other paediatric conditions that occur during the period of time around childbirth, especially the five months before and one month after birth....", "[DD90.4] Functional nausea or vomiting\n Def: Functional nausea and vomiting is a disorder having no structural abnormalities for nausea and vomiting....\n --EXCLUDES--> [?] Nausea or vomiting\n Def: Nausea is the feeling of having an urge to vomit. Vomiting is forcing the contents of the stomach up through the oesophagus and out of the mouth....\n --PARENT--> [?] Symptoms related to the upper gastrointestinal tract\n Def: Clinical symptoms presumed to be arising from disorders/diseases of upper GI tract....", "[DD90.4] Functional nausea or vomiting\n Def: Functional nausea and vomiting is a disorder having no structural abnormalities for nausea and vomiting....\n --RELATED_TO--> [?] Cyclic vomiting syndrome\n Def: Recurrent episodic attacks, usually stereotypical in the individual patient, of vomiting and intense nausea. Attacks are associated with pallor and lethargy. There is complete resolution of symptoms b...\n --PARENT--> [?] Functional nausea or vomiting\n Def: Functional nausea and vomiting is a disorder having no structural abnormalities for nausea and vomiting....", "[ME24.A5] Haematemesis\n Def: Vomiting of blood that is either fresh bright red, or older \"coffee-ground\" in character. Vomiting blood is a regurgitation of blood through the upper gastrointestinal tract and it generally indicates...\n --RELATED_TO--> [?] Neonatal haematemesis or melaena due to swallowed maternal blood\n Def: A less serious, self-limiting case of haematemesis and melena which can occur in newborns two to three days after delivery, due to swallowed maternal blood....\n --PARENT--> [?] Digestive system disorders of fetus or newborn", "[ME24.A5] Haematemesis\n Def: Vomiting of blood that is either fresh bright red, or older \"coffee-ground\" in character. Vomiting blood is a regurgitation of blood through the upper gastrointestinal tract and it generally indicates...\n --RELATED_TO--> [?] Neonatal haematemesis or melaena due to swallowed maternal blood\n Def: A less serious, self-limiting case of haematemesis and melena which can occur in newborns two to three days after delivery, due to swallowed maternal blood....\n --PARENT--> [?] Haematemesis\n Def: Vomiting of blood that is either fresh bright red, or older \"coffee-ground\" in character. Vomiting blood is a regurgitation of blood through the upper gastrointestinal tract and it generally indicates..." ]
MD90.1
Vomiting
[ { "from_icd11": "ME24.A5", "icd10_code": "K920", "icd10_title": "Hematemesis" }, { "from_icd11": "1A23", "icd10_code": "A0811", "icd10_title": "Acute gastroenteropathy due to Norwalk agent" }, { "from_icd11": "1A23", "icd10_code": "A081", "icd10_title": "Acute gastroenteropathy due to Norwalk agent and other small round viruses" }, { "from_icd11": "JA60.Z", "icd10_code": "O218", "icd10_title": "Other vomiting complicating pregnancy" }, { "from_icd11": "JA60.Z", "icd10_code": "O219", "icd10_title": "Vomiting of pregnancy, unspecified" }, { "from_icd11": "JA60.Z", "icd10_code": "O21", "icd10_title": "Excessive vomiting in pregnancy" }, { "from_icd11": "JA60.Z", "icd10_code": "O219 ", "icd10_title": "" }, { "from_icd11": "ND56.0", "icd10_code": "T009", "icd10_title": "" }, { "from_icd11": "ND56.0", "icd10_code": "T140", "icd10_title": "" }, { "from_icd11": "ND56.Z", "icd10_code": "T1491XA", "icd10_title": "Suicide attempt, initial encounter" }, { "from_icd11": "ND56.Z", "icd10_code": "T1490XS", "icd10_title": "Injury, unspecified, sequela" }, { "from_icd11": "ND56.Z", "icd10_code": "T1490", "icd10_title": "Injury, unspecified" }, { "from_icd11": "ND56.Z", "icd10_code": "T1491", "icd10_title": "Suicide attempt" }, { "from_icd11": "ND56.Z", "icd10_code": "T1490XA", "icd10_title": "Injury, unspecified, initial encounter" }, { "from_icd11": "ND56.Z", "icd10_code": "T148XXS", "icd10_title": "Other injury of unspecified body region, sequela" } ]
K920
Hematemesis
The patient was a 79-year-old female farmer with a history of hypertension. She received antihypertensive treatment with oral olmesartan medoxomil tablets once a day, and her blood pressure control was satisfactory. The chief complaint was "weakness in limbs, muscle soreness, and black stool for a week," and she came to our hospital for treatment. One week ago, the patient experienced limb weakness, mainly in both lower limbs, showing symmetrical left and right movements. There was also muscle soreness in both lower limbs, and the strength of both upper limbs was still acceptable. There was no limb movement disorder, accompanied by black stool, with a small amount, and bowel movements were relieved one to two times a day. There was no obvious abdominal pain, no bloody stool, no hemoptysis or vomiting blood, no chest pain or tightness, no fear of cold or fever, decreased appetite, and gradually reduced urine output, ultimately leading to oliguria. The patient denied a history of vigorous activity and physical activity before the onset of the disease. Later, the family sent the patient to a local hospital for treatment, including acid suppression, stomach protection, liver protection, and blood dialysis. The patient's condition continued to progress, and the symptoms of limb weakness worsened, accompanied by drowsiness. The family sent the patient to our hospital for further diagnosis and treatment.
3.333984
0.989258
sec[1]/p[0]
en
0.999998
39483585
https://doi.org/10.7759/cureus.70625
[ "limbs", "blood", "weakness", "stool", "limb", "both", "muscle", "soreness", "black", "movements" ]
[ { "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": "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 === [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 [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 --- [ND56.1] Open wound of unspecified body region --EXCLUDES--> [?] Traumatic amputation of unspecified body region --CHILD--> [?] Sequelae of traumatic amputation of unspecified body region --- Walk 2 --- [ND56.1] Open wound of unspecified body region --EXCLUDES--> [?] Open wounds involving multiple body regions --CHILD--> [?] Open wounds involving head with neck --- 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--> [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--> [FB56.2] Myalgia Def: This is a disorder characterised by pain in a muscle or group of muscles.... --- 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--> [FB56.2] Myalgia Def: This is a disorder characterised by pain in a muscle or group of muscles....
[ "[ND56.1] Open wound of unspecified body region\n --EXCLUDES--> [?] Traumatic amputation of unspecified body region\n --CHILD--> [?] Sequelae of traumatic amputation of unspecified body region", "[ND56.1] Open wound of unspecified body region\n --EXCLUDES--> [?] Open wounds involving multiple body regions\n --CHILD--> [?] Open wounds involving head with neck", "[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--> [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--> [FB56.2] Myalgia\n Def: This is a disorder characterised by pain in a muscle or group of muscles....", "[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--> [FB56.2] Myalgia\n Def: This is a disorder characterised by pain in a muscle or group of muscles...." ]
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
A 30-day-old male infant was transferred to our institution for persistent high-grade fever lasting 16 days. Symptoms started on day 14 of life, and he was admitted to a tertiary-level children’s hospital on the second day of illness, at which time he had no skin, respiratory, gastrointestinal, or nervous system symptoms. Admission laboratory tests revealed a normal complete blood count, serum transaminase levels, albumin, antinuclear antibodies, immunoglobulin levels, and CD markers, but elevated C-reactive protein (CRP) (50 mg/L), erythrocyte sedimentation rate (ESR) (55 mm/h), ferritin (348 ng/ml) and procalcitonin (0.96 ng/ml). His chest X-ray and abdominal ultrasound were unremarkable. Empirical antibiotic therapy comprising of ampicillin and cefotaxime was started for presumed neonatal sepsis. Physical examination was within normal limits except for a transient day-long generalized reddish rash and mild conjunctival congestion on day 6 of fever, which was considered by the neonatologist to be a manifestation of infection. However, bacterial cultures of blood, urine, stool, and cerebrospinal fluid, as well as viral screens for toxoplasmosis, rubella, cytomegalovirus, herpes simplex, adenovirus, respiratory syncytial virus, Influenza A and B, Epstein Barr virus, and rotavirus were all negative. Unfortunately, his fever persisted even after antibiotics were upgraded to vancomycin and meropenem.
3.896484
0.981934
sec[1]/p[0]
en
0.999995
32539746
https://doi.org/10.1186/s12969-020-00440-x
[ "fever", "which", "respiratory", "blood", "virus", "transferred", "institution", "persistent", "grade", "lasting" ]
[ { "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": "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": "CB7Z", "title": "Diseases of the respiratory system, unspecified" } ]
=== 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 [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 [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 === 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 during labour, not elsewhere classified Def: A complication characterised by maternal fever during labour, and not elsewhere classified.... --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--> [?] Disturbances of temperature regulation of newborn Def: Normal body temperature of newborn is 36.5 degrees Celsius (S.D. = 0.6 degrees Celsius). Temperature above 38.0 and below 36.0 may be regarded as unusual and called hyper- and hypothermia respectively... --- 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... --PARENT--> [?] Certain other viral diseases --- Walk 4 --- [1D81.Z] Infectious mononucleosis, unspecified --PARENT--> [1D81] Infectious mononucleosis Def: A disease typically caused by an infection with Epstein-Barr virus or cytomegalovirus. This disease commonly presents with extreme fatigue, fever, acute pharyngitis, body aches, or lymphadenopathy. Tr... --CHILD--> [1D81.1] Mononucleosis due to cytomegalovirus Def: A disease typically caused by an infection with cytomegalovirus. This disease commonly presents with extreme fatigue, fever, acute pharyngitis, body aches, or lymphadenopathy. Transmission is by direc... --- Walk 5 --- [1B99] Pasteurellosis Def: A disease caused by an infection with the gram-negative bacteria Pasteurella. This disease is characterised by local cellulitis and may lead to other clinical signs depending on the route of infection... --PARENT--> [?] Certain zoonotic bacterial diseases Def: This is a group of bacterial diseases that are transmitted to humans by contact with infected vertebrate animals.... --CHILD--> [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... --- 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 during labour, not elsewhere classified\n Def: A complication characterised by maternal fever during labour, and not elsewhere classified....\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--> [?] Disturbances of temperature regulation of newborn\n Def: Normal body temperature of newborn is 36.5 degrees Celsius (S.D. = 0.6 degrees Celsius). Temperature above 38.0 and below 36.0 may be regarded as unusual and called hyper- and hypothermia respectively...", "[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 --PARENT--> [?] Certain other viral diseases", "[1D81.Z] Infectious mononucleosis, unspecified\n --PARENT--> [1D81] Infectious mononucleosis\n Def: A disease typically caused by an infection with Epstein-Barr virus or cytomegalovirus. This disease commonly presents with extreme fatigue, fever, acute pharyngitis, body aches, or lymphadenopathy. Tr...\n --CHILD--> [1D81.1] Mononucleosis due to cytomegalovirus\n Def: A disease typically caused by an infection with cytomegalovirus. This disease commonly presents with extreme fatigue, fever, acute pharyngitis, body aches, or lymphadenopathy. Transmission is by direc...", "[1B99] Pasteurellosis\n Def: A disease caused by an infection with the gram-negative bacteria Pasteurella. This disease is characterised by local cellulitis and may lead to other clinical signs depending on the route of infection...\n --PARENT--> [?] Certain zoonotic bacterial diseases\n Def: This is a group of bacterial diseases that are transmitted to humans by contact with infected vertebrate animals....\n --CHILD--> [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...", "[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
In this study, we present a case of dichorionic diamniotic infants that were delivered via C-section at 30 + 1 weeks due to preterm labor and developed late onset GBS infection and developed neonatal sepsis. Maternal serologies were notable for a negative GBS swab. Initial hospitalization was relatively unremarkable until day of life 33 when twin A began having multiple desaturation events. A complete sepsis evaluation revealed GBS bacteremia. Four days later, twin B also became symptomatic with similar events. Her blood culture also grew GBS. The infants were still in the NICU when the infection occurred. They were being fed primarily fresh expressed maternal breast milk (one child was able to take some small feeds by mouth rather than strictly through NG feeds). The maternal milk was being fortified with formula but was not pasteurized due to the significant loss of nutritional value caused by this process. Maternal expressed breast milk was cultured and grew GBS as well. A short time thereafter, the mother was diagnosed with mastitis. Investigation revealed improper sterilization of breastmilk pump and supplies, with a culture resulting in GBS growth. All GBS isolates were identified as the same organism via pulsed-field gel electrophoresis. The infection was caught by the hospital staff very quickly after onset and therefore did not result in significant clinical deterioration in either child.
4.117188
0.96582
sec[0]/p[7]
en
0.999997
33243275
https://doi.org/10.1186/s12941-020-00396-6
[ "maternal", "infection", "milk", "this", "infants", "onset", "sepsis", "twin", "events", "culture" ]
[ { "code": "6E20", "title": "Mental or behavioural disorders associated with pregnancy, childbirth or the puerperium, without psychotic symptoms" }, { "code": "JA86.Y", "title": "Maternal care for other specified fetal problems" }, { "code": "LD2F.Y", "title": "Other specified syndromes with multiple structural anomalies, without predominant body system involvement" }, { "code": "JA82.6", "title": "Maternal care for compound presentation" }, { "code": "JA8A.0", "title": "Placental transfusion syndromes" }, { "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 === [6E20] Mental or behavioural disorders associated with pregnancy, childbirth or the puerperium, without psychotic symptoms Definition: A syndrome associated with pregnancy or the puerperium (commencing within about 6 weeks after delivery) that involves significant mental and behavioural features, most commonly depressive symptoms. The syndrome does not include delusions, hallucinations, or other psychotic symptoms. If the symptoms meet the diagnostic requirements for a specific mental disorder, that diagnosis should also be assigned. This designation should not be used to describe mild and transient depressive symptoms that do Also known as: Mental or behavioural disorders associated with pregnancy, childbirth or the puerperium, without psychotic symptoms | mental or behavioural disorders associated with pregnancy, childbirth or the puerperium, without psychotic features | Postpartum depression NOS | postnatal depression NOS | puerperal depression NOS [JA86.Y] Maternal care for other specified fetal problems Also known as: Maternal care for other specified fetal problems | Maternal care for other isoimmunization | Isoimmunization NOS | maternal antibodies NOS | pregnancy management affected by incompatibility of blood groups NOS [LD2F.Y] Other specified syndromes with multiple structural anomalies, without predominant body system involvement Also known as: Other specified syndromes with multiple structural anomalies, without predominant body system involvement | Syndromes with multiple structural anomalies of environmental origin | congenital malformation syndromes due to known exogenous causes, not elsewhere classified | Infectious embryofetopathies | Embryofetopathies due to specified maternal conditions [JA82.6] Maternal care for compound presentation Also known as: Maternal care for compound presentation | compound presentation of fetus [JA8A.0] Placental transfusion syndromes Also known as: Placental transfusion syndromes | placental transfusion | placenta transfusion syndrome | Twin to twin transfusion syndrome | Feto-fetal transfusion syndrome [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 --- [6E20] Mental or behavioural disorders associated with pregnancy, childbirth or the puerperium, without psychotic symptoms Def: A syndrome associated with pregnancy or the puerperium (commencing within about 6 weeks after delivery) that involves significant mental and behavioural features, most commonly depressive symptoms. Th... --PARENT--> [?] Mental or behavioural disorders associated with pregnancy, childbirth or the puerperium Def: Syndromes associated with pregnancy or the puerperium (commencing within about 6 weeks after delivery) that involve significant mental and behavioural features. If the symptoms meet the diagnostic req... --CHILD--> [6E21] Mental or behavioural disorders associated with pregnancy, childbirth or the puerperium, with psychotic symptoms Def: A syndrome associated with pregnancy or the puerperium (commencing within about 6 weeks after delivery) that involves significant mental and behavioural features, including delusions, hallucinations, ... --- Walk 2 --- [6E20] Mental or behavioural disorders associated with pregnancy, childbirth or the puerperium, without psychotic symptoms Def: A syndrome associated with pregnancy or the puerperium (commencing within about 6 weeks after delivery) that involves significant mental and behavioural features, most commonly depressive symptoms. Th... --PARENT--> [?] Mental or behavioural disorders associated with pregnancy, childbirth or the puerperium Def: Syndromes associated with pregnancy or the puerperium (commencing within about 6 weeks after delivery) that involve significant mental and behavioural features. If the symptoms meet the diagnostic req... --CHILD--> [6E20] Mental or behavioural disorders associated with pregnancy, childbirth or the puerperium, without psychotic symptoms Def: A syndrome associated with pregnancy or the puerperium (commencing within about 6 weeks after delivery) that involves significant mental and behavioural features, most commonly depressive symptoms. Th... --- Walk 3 --- [JA86.Y] Maternal care for other specified fetal problems --PARENT--> [JA86] 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.... --EXCLUDES--> [?] Placental transfusion syndromes --- Walk 4 --- [JA86.Y] Maternal care for other specified fetal problems --PARENT--> [JA86] 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.... --CHILD--> [JA86.2] Maternal care for signs of fetal hypoxia --- Walk 5 --- [LD2F.Y] Other specified syndromes with multiple structural anomalies, without predominant body system involvement --PARENT--> [LD2F] Syndromes with multiple structural anomalies, without predominant body system involvement --RELATED_TO--> [?] Perinatal Herpes simplex infection Def: Herpes simplex infection acquired during the perinatal period, normally from active herpes infection of the mother's genital tract, but may also be transmitted in utero.... --- Walk 6 --- [LD2F.Y] Other specified syndromes with multiple structural anomalies, without predominant body system involvement --PARENT--> [LD2F] Syndromes with multiple structural anomalies, without predominant body system involvement --RELATED_TO--> [?] Congenital rubella syndrome Def: A disease caused by an infection with the rubella virus in utero. This disease presents with symptoms depending on the timing of infection of the fetus and may present with birth defects (such as hear...
[ "[6E20] Mental or behavioural disorders associated with pregnancy, childbirth or the puerperium, without psychotic symptoms\n Def: A syndrome associated with pregnancy or the puerperium (commencing within about 6 weeks after delivery) that involves significant mental and behavioural features, most commonly depressive symptoms. Th...\n --PARENT--> [?] Mental or behavioural disorders associated with pregnancy, childbirth or the puerperium\n Def: Syndromes associated with pregnancy or the puerperium (commencing within about 6 weeks after delivery) that involve significant mental and behavioural features. If the symptoms meet the diagnostic req...\n --CHILD--> [6E21] Mental or behavioural disorders associated with pregnancy, childbirth or the puerperium, with psychotic symptoms\n Def: A syndrome associated with pregnancy or the puerperium (commencing within about 6 weeks after delivery) that involves significant mental and behavioural features, including delusions, hallucinations, ...", "[6E20] Mental or behavioural disorders associated with pregnancy, childbirth or the puerperium, without psychotic symptoms\n Def: A syndrome associated with pregnancy or the puerperium (commencing within about 6 weeks after delivery) that involves significant mental and behavioural features, most commonly depressive symptoms. Th...\n --PARENT--> [?] Mental or behavioural disorders associated with pregnancy, childbirth or the puerperium\n Def: Syndromes associated with pregnancy or the puerperium (commencing within about 6 weeks after delivery) that involve significant mental and behavioural features. If the symptoms meet the diagnostic req...\n --CHILD--> [6E20] Mental or behavioural disorders associated with pregnancy, childbirth or the puerperium, without psychotic symptoms\n Def: A syndrome associated with pregnancy or the puerperium (commencing within about 6 weeks after delivery) that involves significant mental and behavioural features, most commonly depressive symptoms. Th...", "[JA86.Y] Maternal care for other specified fetal problems\n --PARENT--> [JA86] 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....\n --EXCLUDES--> [?] Placental transfusion syndromes", "[JA86.Y] Maternal care for other specified fetal problems\n --PARENT--> [JA86] 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....\n --CHILD--> [JA86.2] Maternal care for signs of fetal hypoxia", "[LD2F.Y] Other specified syndromes with multiple structural anomalies, without predominant body system involvement\n --PARENT--> [LD2F] Syndromes with multiple structural anomalies, without predominant body system involvement\n --RELATED_TO--> [?] Perinatal Herpes simplex infection\n Def: Herpes simplex infection acquired during the perinatal period, normally from active herpes infection of the mother's genital tract, but may also be transmitted in utero....", "[LD2F.Y] Other specified syndromes with multiple structural anomalies, without predominant body system involvement\n --PARENT--> [LD2F] Syndromes with multiple structural anomalies, without predominant body system involvement\n --RELATED_TO--> [?] Congenital rubella syndrome\n Def: A disease caused by an infection with the rubella virus in utero. This disease presents with symptoms depending on the timing of infection of the fetus and may present with birth defects (such as hear..." ]
6E20
Mental or behavioural disorders associated with pregnancy, childbirth or the puerperium, without psychotic symptoms
[ { "from_icd11": "6E20", "icd10_code": "F53", "icd10_title": "Mental and behavioral disorders associated with the puerperium, not elsewhere classified" }, { "from_icd11": "JA86.Y", "icd10_code": "O26841 ", "icd10_title": "" }, { "from_icd11": "JA86.Y", "icd10_code": "O26843 ", "icd10_title": "" }, { "from_icd11": "JA86.Y", "icd10_code": "O26849 ", "icd10_title": "" }, { "from_icd11": "JA86.Y", "icd10_code": "O3680X0 ", "icd10_title": "" }, { "from_icd11": "LD2F.Y", "icd10_code": "Q8789 ", "icd10_title": "" }, { "from_icd11": "JA82.6", "icd10_code": "O326XX0", "icd10_title": "Maternal care for compound presentation, not applicable or unspecified" }, { "from_icd11": "JA82.6", "icd10_code": "O326", "icd10_title": "Maternal care for compound presentation" }, { "from_icd11": "JA8A.0", "icd10_code": "O43022", "icd10_title": "Fetus-to-fetus placental transfusion syndrome, second trimester" }, { "from_icd11": "JA8A.0", "icd10_code": "O430", "icd10_title": "Placental transfusion syndromes" }, { "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" } ]
F53
Mental and behavioral disorders associated with the puerperium, not elsewhere classified
Patient 2 (P2) : A 51‐year‐old male underwent cadaveric renal transplantation for polycystic kidney disease. He developed EBV+ monomorphic PTLD 2 months post‐SOT which was refractory to six lines of treatment (detailed in Table S1 ). His latest line of therapy was one cycle of RBP, delivered 32 days prior to apheresis. IS comprised prednisolone monotherapy (20 mg/day). Pre‐leukapheresis, his PB lymphocyte and CD3+ T‐cell counts were 0.24 × 10 9 /L and 0.11 × 10 9 /L. His lymphocyte count had been consistently ≤0.3 × 10 9 /L for >1 year after steroids/prior therapies, and the total CD3+ T‐cell yield from leukapheresis was 1.39 × 10 9 . The resulting CAR‐T product was out‐of‐specification (OOS) due to low cell viability (71% against a specification of ≥80%) but was approved for infusion due to rapidly progressive disease. Bridging comprised RBP to PD, and 20 Gy radiotherapy to the oropharynx/thorax . The patient received Flu/Cy/CAR‐T infusion and continued prednisolone (10 mg/day) with normal renal function throughout. He developed G1 CRS on day 3 and slurred speech on day 6, presumed ICANS, and received 6‐hourly dexamethasone 10 mg, but his neurological status continued to deteriorate. CSF analysis revealed clonal B‐cells and MRI brain/spine confirmed neurological involvement by PTLD . Due to rapidly progressive, debilitating disease, the patient opted for palliative care and passed away on day 30.
4.027344
0.972656
sec[0]/p[4]
en
0.999997
39981112
https://doi.org/10.1002/jha2.70006
[ "cell", "renal", "ptld", "comprised", "prednisolone", "leukapheresis", "lymphocyte", "specification", "infusion", "rapidly" ]
[ { "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": "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" } ]
=== ICD-11 CODES FOUND === [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 [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 === GRAPH WALKS === --- Walk 1 --- [MF9Y] Other specified clinical findings on examination of urine, without diagnosis --PARENT--> [?] Clinical findings on examination of urine, without diagnosis --EXCLUDES--> [?] Clinical findings on antenatal screening of mother Def: Any sign characterised by an abnormality detected during an antenatal screening of the mother.... --- Walk 2 --- [MF9Y] Other specified clinical findings on examination of urine, without diagnosis --PARENT--> [?] Clinical findings on examination of urine, without diagnosis --CHILD--> [MF91] Bilirubinuria Def: Bilirubinuria means the presence of any bile pigment in the urine.... --- Walk 3 --- [5C56.20] Mucolipidosis --RELATED_TO--> [?] Mucolipidosis type 4 Def: Mucolipidosis type IV (ML IV) is a lysosomal storage disease characterised clinically by psychomotor retardation and visual abnormalities including corneal clouding, retinal degeneration, or strabismu... --PARENT--> [?] Mucolipidosis --- Walk 4 --- [5C56.20] Mucolipidosis --RELATED_TO--> [?] Wolman disease Def: Wolman disease represents the most severe manifestation of lysosomal acid lipase deficiency and can present in the fetus (hepatomegaly, ascites, calcified adrenal glands), or more typically in the fir... --PARENT--> [?] Lysosomal acid lipase deficiency Def: Lysosomal Acid Lipase (LAL) Deficiency happens when the body does not produce enough active lysosomal acid lipase (LAL or LIPA) enzyme. This enzyme plays an important role in breaking down fatty mater... --- Walk 5 --- [3A51.1] Sickle cell disease without crisis Def: A disorder caused by a HbS mutation in the haemoglobin gene. This disorder is characterised by abnormal rigid sickle-shaped red blood cells decreasing its ability to carry oxygen. This disorder may pr... --PARENT--> [3A51] Sickle cell disorders or other haemoglobinopathies Def: Any disorder caused by a HbS mutation in the haemoglobin gene. This disorder is characterised by abnormal rigid sickle-shaped red blood cells decreasing its ability to carry oxygen. This disorder may ... --RELATED_TO--> [?] Osteonecrosis due to haemoglobinopathy --- Walk 6 --- [3A51.1] Sickle cell disease without crisis Def: A disorder caused by a HbS mutation in the haemoglobin gene. This disorder is characterised by abnormal rigid sickle-shaped red blood cells decreasing its ability to carry oxygen. This disorder may pr... --PARENT--> [3A51] Sickle cell disorders or other haemoglobinopathies Def: Any disorder caused by a HbS mutation in the haemoglobin gene. This disorder is characterised by abnormal rigid sickle-shaped red blood cells decreasing its ability to carry oxygen. This disorder may ... --CHILD--> [3A51.0] Sickle cell trait Def: A disease caused by genetic inheritance of one abnormal allele of the haemoglobin gene. This disease does not display the severe symptoms of sickle cell disease that occurs in homozygous individuals. ...
[ "[MF9Y] Other specified clinical findings on examination of urine, without diagnosis\n --PARENT--> [?] Clinical findings on examination of urine, without diagnosis\n --EXCLUDES--> [?] Clinical findings on antenatal screening of mother\n Def: Any sign characterised by an abnormality detected during an antenatal screening of the mother....", "[MF9Y] Other specified clinical findings on examination of urine, without diagnosis\n --PARENT--> [?] Clinical findings on examination of urine, without diagnosis\n --CHILD--> [MF91] Bilirubinuria\n Def: Bilirubinuria means the presence of any bile pigment in the urine....", "[5C56.20] Mucolipidosis\n --RELATED_TO--> [?] Mucolipidosis type 4\n Def: Mucolipidosis type IV (ML IV) is a lysosomal storage disease characterised clinically by psychomotor retardation and visual abnormalities including corneal clouding, retinal degeneration, or strabismu...\n --PARENT--> [?] Mucolipidosis", "[5C56.20] Mucolipidosis\n --RELATED_TO--> [?] Wolman disease\n Def: Wolman disease represents the most severe manifestation of lysosomal acid lipase deficiency and can present in the fetus (hepatomegaly, ascites, calcified adrenal glands), or more typically in the fir...\n --PARENT--> [?] Lysosomal acid lipase deficiency\n Def: Lysosomal Acid Lipase (LAL) Deficiency happens when the body does not produce enough active lysosomal acid lipase (LAL or LIPA) enzyme. This enzyme plays an important role in breaking down fatty mater...", "[3A51.1] Sickle cell disease without crisis\n Def: A disorder caused by a HbS mutation in the haemoglobin gene. This disorder is characterised by abnormal rigid sickle-shaped red blood cells decreasing its ability to carry oxygen. This disorder may pr...\n --PARENT--> [3A51] Sickle cell disorders or other haemoglobinopathies\n Def: Any disorder caused by a HbS mutation in the haemoglobin gene. This disorder is characterised by abnormal rigid sickle-shaped red blood cells decreasing its ability to carry oxygen. This disorder may ...\n --RELATED_TO--> [?] Osteonecrosis due to haemoglobinopathy", "[3A51.1] Sickle cell disease without crisis\n Def: A disorder caused by a HbS mutation in the haemoglobin gene. This disorder is characterised by abnormal rigid sickle-shaped red blood cells decreasing its ability to carry oxygen. This disorder may pr...\n --PARENT--> [3A51] Sickle cell disorders or other haemoglobinopathies\n Def: Any disorder caused by a HbS mutation in the haemoglobin gene. This disorder is characterised by abnormal rigid sickle-shaped red blood cells decreasing its ability to carry oxygen. This disorder may ...\n --CHILD--> [3A51.0] Sickle cell trait\n Def: A disease caused by genetic inheritance of one abnormal allele of the haemoglobin gene. This disease does not display the severe symptoms of sickle cell disease that occurs in homozygous individuals. ..." ]
MF9Y
Other specified clinical findings on examination of urine, without diagnosis
[ { "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]" }, { "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" } ]
D571
Sickle-cell disease without crisis
Patient CA106 is a 39-year-old male who was referred for evaluation of elevated serum Ca2+ and PTH levels in several routine blood laboratory analyses and hypocalciuria. Laboratory results showed serum Ca2+ of 10.2 to 10.8 mg/dL (reference range 8.5–10.4) and high intact PTH levels (93–128 pg/mL, reference range 10–65), whereas serum phosphate (3.5 mg/dL, reference range 2.6–4.8) and 25-hydroxyvitamin D levels (39 ng/mL, reference range 9–47) were within the normal range. He was clinically diagnosed of Familial hypocalciuric hypercalcemia, therefore the CASR , AP2S1 and GNA11 genes were requested for genetics analysis. Furthermore, patient CA106 had a personal history of idiopathic panhypopituitarism on substitutive hormonal treatment except growth hormone, skin sarcoma (dermatofibrosarcoma protuberans), high blood pressure, basilar artery fenestration, and he had a sprain in the wrist and back pain. We did not find alterations in the proposed genes by NGS, but we found a novel likely pathogenic variant in the heterozygous state in the CNNM2 gene. Therefore, a new laboratory evaluation was requested confirming the previous results and the presence of moderate hypomagnesemia (1.38 mg/dL, reference range 1.7–2.5). Furthermore, hypomagnesemia was observed within his family as well (sister and mother showed hypomagnesemia, 1.32 mg/dL and 1.42 mg/dL respectively). Both had the variant carried by CA106.
4.078125
0.962891
sec[2]/sec[0]/p[0]
en
0.999995
32997713
https://doi.org/10.1371/journal.pone.0239965
[ "range", "reference", "serum", "laboratory", "hypomagnesemia", "blood", "within", "therefore", "genes", "requested" ]
[ { "code": "QA00.6Y", "title": "Other specified examination of eyes or vision" }, { "code": "4B00.0Z", "title": "Neutropaenia, unspecified" }, { "code": "3B63.1Z", "title": "Acquired thrombocytosis, unspecified" }, { "code": "MA14.1C", "title": "Raised antibody titre" }, { "code": "BD11.1", "title": "Left ventricular failure with mid range ejection fraction" }, { "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": "NE80.3", "title": "Other serum reactions" }, { "code": "5D0Y", "title": "Other specified metabolic disorders" } ]
=== ICD-11 CODES FOUND === [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 [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 [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 [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 [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 [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 === GRAPH WALKS === --- Walk 1 --- [QA00.6Y] Other specified examination of eyes or vision --PARENT--> [QA00.6] Examination of eyes or vision --EXCLUDES--> [?] Examination for driving license --- Walk 2 --- [QA00.6Y] Other specified examination of eyes or vision --PARENT--> [QA00.6] Examination of eyes or vision --CHILD--> [QA00.61] Normal Visual Field --- Walk 3 --- [4B00.0Z] Neutropaenia, unspecified --PARENT--> [4B00.0] Neutropenia --PARENT--> [4B00] Disorders of neutrophil number --- Walk 4 --- [4B00.0Z] Neutropaenia, unspecified --PARENT--> [4B00.0] Neutropenia --RELATED_TO--> [?] Alloimmune neonatal neutropaenia Def: Alloimmune neonatal neutropaenia (ANN) is a disease caused by the passive transfer of neutrophil specific maternal IgG antibodies across the placenta during pregnancy.... --- Walk 5 --- [3B63.1Z] Acquired thrombocytosis, unspecified --PARENT--> [3B63.1] Acquired thrombocytosis Def: A chronic myeloproliferative neoplasm that involves primarily the megakaryocytic lineage. It is characterised by sustained thrombocytosis in the blood, increased numbers of large, mature megakaryocyte... --CHILD--> [3B63.1Y] Other specified acquired thrombocytosis --- Walk 6 --- [3B63.1Z] Acquired thrombocytosis, unspecified --PARENT--> [3B63.1] Acquired thrombocytosis Def: A chronic myeloproliferative neoplasm that involves primarily the megakaryocytic lineage. It is characterised by sustained thrombocytosis in the blood, increased numbers of large, mature megakaryocyte... --CHILD--> [3B63.1Y] Other specified acquired thrombocytosis
[ "[QA00.6Y] Other specified examination of eyes or vision\n --PARENT--> [QA00.6] Examination of eyes or vision\n --EXCLUDES--> [?] Examination for driving license", "[QA00.6Y] Other specified examination of eyes or vision\n --PARENT--> [QA00.6] Examination of eyes or vision\n --CHILD--> [QA00.61] Normal Visual Field", "[4B00.0Z] Neutropaenia, unspecified\n --PARENT--> [4B00.0] Neutropenia\n --PARENT--> [4B00] Disorders of neutrophil number", "[4B00.0Z] Neutropaenia, unspecified\n --PARENT--> [4B00.0] Neutropenia\n --RELATED_TO--> [?] Alloimmune neonatal neutropaenia\n Def: Alloimmune neonatal neutropaenia (ANN) is a disease caused by the passive transfer of neutrophil specific maternal IgG antibodies across the placenta during pregnancy....", "[3B63.1Z] Acquired thrombocytosis, unspecified\n --PARENT--> [3B63.1] Acquired thrombocytosis\n Def: A chronic myeloproliferative neoplasm that involves primarily the megakaryocytic lineage. It is characterised by sustained thrombocytosis in the blood, increased numbers of large, mature megakaryocyte...\n --CHILD--> [3B63.1Y] Other specified acquired thrombocytosis", "[3B63.1Z] Acquired thrombocytosis, unspecified\n --PARENT--> [3B63.1] Acquired thrombocytosis\n Def: A chronic myeloproliferative neoplasm that involves primarily the megakaryocytic lineage. It is characterised by sustained thrombocytosis in the blood, increased numbers of large, mature megakaryocyte...\n --CHILD--> [3B63.1Y] Other specified acquired thrombocytosis" ]
QA00.6Y
Other specified examination of eyes or vision
[ { "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": "6B22.Z", "icd10_code": "F428", "icd10_title": "Other obsessive-compulsive disorder" }, { "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" } ]
D473
Essential (hemorrhagic) thrombocythemia
The patient failed multiple conservative treatments for his bilateral foot pain, including gabapentinoid and non-steroidal anti-inflammatory medications. He experienced back pain relief from lumbar medial branch blocks and radiofrequency ablations. However, the corticosteroids would consistently elevate his blood glucose concentrations for several days after these procedures. Considering we were unable to effectively treat his foot pain, combined with the blood glucose elevation from the corticosteroids used for his back pain treatment, we explored other treatment options to address both problems effectively. We offered the patient a trial of DRG-S, given our positive experience with DRG-S for both neuropathic pain and axial low back pain, after he received psychological evaluation clearance for his baseline depression and anxiety. As per usual practice at our institute, regardless of bilateral symptoms, we performed a unilateral stimulation trial for seven days. A unilateral trial has several advantages over a bilateral one, including the ability for the patient to compare the treated side with the untreated side and a decreased risk of complications and post-procedural pain. Leads were trialed at the right T12 and S1 to cover the low back and distal extremity pain . During the single-sided trial, DRG-S settings included a frequency of 20 Hz, a pulse width of 260 us, and an amplitude of 0.425 mA.
3.914063
0.943359
sec[1]/p[1]
en
0.999996
33145140
https://doi.org/10.7759/cureus.10735
[ "pain", "back", "trial", "foot", "including", "corticosteroids", "blood", "glucose", "several", "effectively" ]
[ { "code": "MG3Z", "title": "Pain, unspecified" }, { "code": "8E43.Z", "title": "Pain disorders, unspecified" }, { "code": "MG31.Z", "title": "Acute pain, unspecified" }, { "code": "MG30.Z", "title": "Chronic pain, unspecified" }, { "code": "FB56.2", "title": "Myalgia" }, { "code": "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" } ]
=== ICD-11 CODES FOUND === [MG3Z] Pain, unspecified Also known as: Pain, unspecified | pain observations | pain NOS | generalised pain | generalised pain, NOS [8E43.Z] Pain disorders, unspecified Also known as: Pain disorders, unspecified | Pain disorders [MG31.Z] Acute pain, unspecified Also known as: Acute pain, unspecified | Acute pain [MG30.Z] Chronic pain, unspecified Also known as: Chronic pain, unspecified | Chronic pain [FB56.2] Myalgia Definition: This is a disorder characterised by pain in a muscle or group of muscles. Also known as: Myalgia | muscle ache | muscle soreness | muscular pain | myalgic Excludes: Chronic primary musculoskeletal pain | Chronic secondary musculoskeletal pain [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 === GRAPH WALKS === --- Walk 1 --- [MG3Z] Pain, unspecified --PARENT--> [?] Pain --EXCLUDES--> [?] Headache disorders --- Walk 2 --- [MG3Z] Pain, unspecified --PARENT--> [?] Pain --EXCLUDES--> [?] Abdominal or pelvic pain Def: Pain, an unpleasant distress sensation occurring in varying degrees of severity, received by nerve ending in the abdominal and pelvic region.... --- Walk 3 --- [8E43.Z] Pain disorders, unspecified --PARENT--> [8E43] Pain disorders --EXCLUDES--> [?] Chronic neuropathic pain Def: Chronic neuropathic pain is chronic pain caused by a lesion or disease of the somatosensory nervous system. The pain may be spontaneous or evoked, as an increased response to a painful stimulus (hyper... --- Walk 4 --- [8E43.Z] Pain disorders, unspecified --PARENT--> [8E43] Pain disorders --EXCLUDES--> [?] Chronic neuropathic pain Def: Chronic neuropathic pain is chronic pain caused by a lesion or disease of the somatosensory nervous system. The pain may be spontaneous or evoked, as an increased response to a painful stimulus (hyper... --- Walk 5 --- [MG31.Z] Acute pain, unspecified --PARENT--> [MG31] Acute pain Def: Pain with a duration of less than 3 months. This code should be used only when there is no further specification of site.... --CHILD--> [MG31.0] Acute pain in the face, not elsewhere classified --- Walk 6 --- [MG31.Z] Acute pain, unspecified --PARENT--> [MG31] Acute pain Def: Pain with a duration of less than 3 months. This code should be used only when there is no further specification of site.... --CHILD--> [MG31.0] Acute pain in the face, not elsewhere classified
[ "[MG3Z] Pain, unspecified\n --PARENT--> [?] Pain\n --EXCLUDES--> [?] Headache disorders", "[MG3Z] Pain, unspecified\n --PARENT--> [?] Pain\n --EXCLUDES--> [?] Abdominal or pelvic pain\n Def: Pain, an unpleasant distress sensation occurring in varying degrees of severity, received by nerve ending in the abdominal and pelvic region....", "[8E43.Z] Pain disorders, unspecified\n --PARENT--> [8E43] Pain disorders\n --EXCLUDES--> [?] Chronic neuropathic pain\n Def: Chronic neuropathic pain is chronic pain caused by a lesion or disease of the somatosensory nervous system. The pain may be spontaneous or evoked, as an increased response to a painful stimulus (hyper...", "[8E43.Z] Pain disorders, unspecified\n --PARENT--> [8E43] Pain disorders\n --EXCLUDES--> [?] Chronic neuropathic pain\n Def: Chronic neuropathic pain is chronic pain caused by a lesion or disease of the somatosensory nervous system. The pain may be spontaneous or evoked, as an increased response to a painful stimulus (hyper...", "[MG31.Z] Acute pain, unspecified\n --PARENT--> [MG31] Acute pain\n Def: Pain with a duration of less than 3 months.\n\nThis code should be used only when there is no further specification of site....\n --CHILD--> [MG31.0] Acute pain in the face, not elsewhere classified", "[MG31.Z] Acute pain, unspecified\n --PARENT--> [MG31] Acute pain\n Def: Pain with a duration of less than 3 months.\n\nThis code should be used only when there is no further specification of site....\n --CHILD--> [MG31.0] Acute pain in the face, not elsewhere classified" ]
MG3Z
Pain, unspecified
[ { "from_icd11": "MG3Z", "icd10_code": "R52", "icd10_title": "Pain, unspecified" }, { "from_icd11": "MG3Z", "icd10_code": "R529", "icd10_title": "" }, { "from_icd11": "MG31.Z", "icd10_code": "R520", "icd10_title": "" }, { "from_icd11": "MG30.Z", "icd10_code": "R521", "icd10_title": "" }, { "from_icd11": "MG30.Z", "icd10_code": "R522", "icd10_title": "" }, { "from_icd11": "FB56.2", "icd10_code": "M7918", "icd10_title": "Myalgia, other site" }, { "from_icd11": "FB56.2", "icd10_code": "M7910", "icd10_title": "Myalgia, unspecified site" }, { "from_icd11": "FB56.2", "icd10_code": "M7912", "icd10_title": "Myalgia of auxiliary muscles, head and neck" }, { "from_icd11": "FB56.2", "icd10_code": "M791", "icd10_title": "Myalgia" }, { "from_icd11": "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" } ]
R52
Pain, unspecified
Here, we describe two cases of an unusual triple infection with M. tuberculosis , HIV, and SARS-CoV-2 in Panama. We describe the clinical management, therapy, and progression of both cases that allowed for recovery from COVID-19. On admission, the standard of care for COVID-19 patients in this hospital included critical status assessment, invasive mechanical ventilation for severe cases, and clinical management with oxygen by the nasal canula for mild and moderate cases. In these two reported cases, acute respiratory failure triggered by COVID-19 was promptly addressed. This strategy facilitated rapid recovery despite a triple infection. We used HCQ to treat both cases as recommended by the WHO Solidarity clinical trial, which was ongoing at the time of the patients’ admission. Unfortunately, recent evidence has raised concerns about HCQ, and the WHO has recommended against its use. 1 To date, there have been no similar reports of patients presenting with three concomitant infectious diseases. However, reports describe cases of people living with HIV affected by previous SARS, Middle East respiratory coronavirus, and COVID outbreaks. These case reports of people coinfected with HIV affirm that these patients recover most of the time. Although other authors have separately reported coinfection with tuberulosis (TB), 2 our study analyzed the progression of triple infection during the COVID pandemic.
4.15625
0.718262
sec[1]/p[0]
en
0.999998
32815513
https://doi.org/10.4269/ajtmh.20-0756
[ "cases", "covid", "patients", "describe", "triple", "infection", "these", "sars", "progression", "both" ]
[ { "code": "JB20.Z", "title": "Single spontaneous delivery, unspecified" }, { "code": "QA48.0", "title": "Care or examination immediately after delivery" }, { "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" }, { "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" } ]
=== ICD-11 CODES FOUND === [JB20.Z] Single spontaneous delivery, unspecified Also known as: Single spontaneous delivery, unspecified | Single spontaneous delivery | spontaneous delivery NOS | normal delivery NOS | uncomplicated delivery [QA48.0] Care or examination immediately after delivery Also known as: Care or examination immediately after delivery | care and observation in uncomplicated delivery cases | postpartum care immediately after delivery | postpartum examination immediately after delivery | Postpartum care after hospital delivery Excludes: Complications predominantly related to the puerperium [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 [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 === GRAPH WALKS === --- Walk 1 --- [JB20.Z] Single spontaneous delivery, unspecified --PARENT--> [JB20] Single spontaneous delivery Def: A condition caused by the development of a fetus to the culmination of the pregnancy period. This condition is characterised by spontaneous parturition of a neonate from the uterus.... --CHILD--> [JB20.1] Spontaneous breech delivery Def: A condition caused by the development of a fetus to the culmination of the pregnancy period. This condition is characterised by spontaneous parturition of a neonate in breech position from the uterus.... --- Walk 2 --- [JB20.Z] Single spontaneous delivery, unspecified --PARENT--> [JB20] Single spontaneous delivery Def: A condition caused by the development of a fetus to the culmination of the pregnancy period. This condition is characterised by spontaneous parturition of a neonate from the uterus.... --CHILD--> [JB20.1] Spontaneous breech delivery Def: A condition caused by the development of a fetus to the culmination of the pregnancy period. This condition is characterised by spontaneous parturition of a neonate in breech position from the uterus.... --- Walk 3 --- [QA48.0] Care or examination immediately after delivery --EXCLUDES--> [?] Complications predominantly related to the puerperium Def: A group of conditions characterised as any adverse evolution (complication) which may arise during the approximately six weeks after delivery during which the uterus returns to the original size (puer... --EXCLUDES--> [?] Obstetrical tetanus Def: A disease caused by an infection with the gram-positive bacteria Clostridium tetani. This disease is characterised by a prolonged contraction of skeletal muscle fibres during pregnancy or within six w... --- Walk 4 --- [QA48.0] Care or examination immediately after delivery --EXCLUDES--> [?] Complications predominantly related to the puerperium Def: A group of conditions characterised as any adverse evolution (complication) which may arise during the approximately six weeks after delivery during which the uterus returns to the original size (puer... --CHILD--> [?] Venous complications in the puerperium --- Walk 5 --- [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 6 --- [RA01.0] 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... --PARENT--> [?] Pneumonia Def: A disease of the lungs, frequently but not always caused by an infection with bacteria, virus, fungus, or parasite. This disease is characterised by fever, chills, cough with sputum production, chest ...
[ "[JB20.Z] Single spontaneous delivery, unspecified\n --PARENT--> [JB20] Single spontaneous delivery\n Def: A condition caused by the development of a fetus to the culmination of the pregnancy period. This condition is characterised by spontaneous parturition of a neonate from the uterus....\n --CHILD--> [JB20.1] Spontaneous breech delivery\n Def: A condition caused by the development of a fetus to the culmination of the pregnancy period. This condition is characterised by spontaneous parturition of a neonate in breech position from the uterus....", "[JB20.Z] Single spontaneous delivery, unspecified\n --PARENT--> [JB20] Single spontaneous delivery\n Def: A condition caused by the development of a fetus to the culmination of the pregnancy period. This condition is characterised by spontaneous parturition of a neonate from the uterus....\n --CHILD--> [JB20.1] Spontaneous breech delivery\n Def: A condition caused by the development of a fetus to the culmination of the pregnancy period. This condition is characterised by spontaneous parturition of a neonate in breech position from the uterus....", "[QA48.0] Care or examination immediately after delivery\n --EXCLUDES--> [?] Complications predominantly related to the puerperium\n Def: A group of conditions characterised as any adverse evolution (complication) which may arise during the approximately six weeks after delivery during which the uterus returns to the original size (puer...\n --EXCLUDES--> [?] Obstetrical tetanus\n Def: A disease caused by an infection with the gram-positive bacteria Clostridium tetani. This disease is characterised by a prolonged contraction of skeletal muscle fibres during pregnancy or within six w...", "[QA48.0] Care or examination immediately after delivery\n --EXCLUDES--> [?] Complications predominantly related to the puerperium\n Def: A group of conditions characterised as any adverse evolution (complication) which may arise during the approximately six weeks after delivery during which the uterus returns to the original size (puer...\n --CHILD--> [?] Venous complications in the puerperium", "[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--> [?] 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 --PARENT--> [?] Pneumonia\n Def: A disease of the lungs, frequently but not always caused by an infection with bacteria, virus, fungus, or parasite. This disease is characterised by fever, chills, cough with sputum production, chest ..." ]
JB20.Z
Single spontaneous delivery, unspecified
[ { "from_icd11": "JB20.Z", "icd10_code": "O80", "icd10_title": "Encounter for full-term uncomplicated delivery" }, { "from_icd11": "JB20.Z", "icd10_code": "O808", "icd10_title": "" }, { "from_icd11": "JB20.Z", "icd10_code": "O809", "icd10_title": "" }, { "from_icd11": "QA48.0", "icd10_code": "Z390", "icd10_title": "Encounter for care and examination of mother immediately after delivery" }, { "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": "QB14", "icd10_code": "Z753", "icd10_title": "Unavailability and inaccessibility of health-care facilities" } ]
O80
Encounter for full-term uncomplicated delivery
Although our patient did experience visual loss, there were no other classic symptoms or elevation of routine acute phase reactants in him. One multi-center retrospective trial has found CRP to have a higher sensitivity than ESR (61 versus 71%) and a specificity of 57% for ESR versus 68% for CRP . To date, there are no studies in the literature that have examined the role of high-sensitivity CRP in the diagnosis of GCA. This may be attributed to the fact its utility mainly lies in cardiovascular disease and in the prediction of cardiovascular morbidities and mortality . Its role is of particular interest in atypical cases such as this one, where the routine acute phase reactants remain normal and a more sensitive marker is required. Delayed filling in the choroidal circulation was absent in either eye on the original fluorescein angiogram done within one day of visual loss. Delayed filling in the choroidal circulation has been described as a diagnostic feature of GCA and implies ischemia affecting the tributaries of the posterior ciliary circulation, which are branches of the ophthalmic artery. The MRI showed enhancement of the left optic nerve sheaths, suggestive of a perineuritis . Perineuritis has a multitude of etiologies including sarcoidosis, GCA, granulomatosis with polyangiitis, neurosyphilis, tuberculosis, and idiopathic causes. Recent studies have reported its rare association with GCA .
4.1875
0.487549
sec[2]/p[1]
en
0.999999
32775116
https://doi.org/10.7759/cureus.9530
[ "circulation", "visual", "loss", "routine", "phase", "reactants", "sensitivity", "versus", "role", "this" ]
[ { "code": "MG40.Z", "title": "Shock, unspecified" }, { "code": "BE2Z", "title": "Diseases of the circulatory system, unspecified" }, { "code": "KB42", "title": "Persistent pulmonary hypertension of the newborn" }, { "code": "3B21.Z", "title": "Haemorrhagic disorder due to unspecified circulating anticoagulants or coagulation factors" }, { "code": "BE2Y", "title": "Other specified diseases of the circulatory system" }, { "code": "9E1Z", "title": "Diseases of the visual system, unspecified" }, { "code": "MC1Y", "title": "Other specified symptoms or signs involving the visual system" }, { "code": "9D9Z", "title": "Vision impairment, unspecified" }, { "code": "9D90.2", "title": "Moderate vision impairment" }, { "code": "QA00.6Z", "title": "Examination of eyes or vision, unspecified" } ]
=== ICD-11 CODES FOUND === [MG40.Z] Shock, unspecified Also known as: Shock, unspecified | Shock | acute circulatory failure | circulatory collapse | collapse cardiovascular [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 [KB42] Persistent pulmonary hypertension of the newborn Definition: Persistent pulmonary hypertension of the newborn is a cardiopulmonary disorder characterised by systemic arterial hypoxemia secondary to pulmonary hypertension and extrapulmonary right-to-left shunting across the foramen ovale and ductus arteriosus. Also known as: Persistent pulmonary hypertension of the newborn | persistent fetal circulation syndrome | fetal circulation | PFC - [persistent fetal circulation] syndrome | PPHN - [Persistent pulmonary hypertension of the newborn] [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 [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 [9E1Z] Diseases of the visual system, unspecified Also known as: Diseases of the visual system, unspecified | eye diseases NOS | disorder of vision | visual disorder [MC1Y] Other specified symptoms or signs involving the visual system Also known as: Other specified symptoms or signs involving the visual system | Erythema of eyelid | Visual disturbances | disturbances of vision | difficulty seeing [9D9Z] Vision impairment, unspecified Also known as: Vision impairment, unspecified | sight impaired | blindness and low vision | impaired vision [9D90.2] Moderate vision impairment Also known as: Moderate vision impairment | low vision, both eyes | visual impairment category 2, in both eyes | Low vision | LW - [low vision] Includes: visual impairment category 2, in both eyes [QA00.6Z] Examination of eyes or vision, unspecified Also known as: Examination of eyes or vision, unspecified | Examination of eyes or vision | general eye examination | routine eye examination | vision examination === GRAPH WALKS === --- Walk 1 --- [MG40.Z] Shock, unspecified --PARENT--> [MG40] Shock Def: Shock is a life-threatening medical condition that occurs due to inadequate substrate for aerobic cellular respiration. In the early stages this is generally an inadequate tissue level of oxygen. Shoc... --CHILD--> [MG40.Y] Other specified shock --- Walk 2 --- [MG40.Z] Shock, unspecified --PARENT--> [MG40] Shock Def: Shock is a life-threatening medical condition that occurs due to inadequate substrate for aerobic cellular respiration. In the early stages this is generally an inadequate tissue level of oxygen. Shoc... --RELATED_TO--> [?] Shock following abortion, ectopic or molar pregnancy --- Walk 3 --- [BE2Z] Diseases of the circulatory system, unspecified --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 4 --- [BE2Z] Diseases of the circulatory system, unspecified --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... --RELATED_TO--> [?] Functional vascular disorders of the skin Def: Skin disorders due to disturbances in vascular tone and skin blood flow.... --- Walk 5 --- [KB42] Persistent pulmonary hypertension of the newborn Def: Persistent pulmonary hypertension of the newborn is a cardiopulmonary disorder characterised by systemic arterial hypoxemia secondary to pulmonary hypertension and extrapulmonary right-to-left shuntin... --PARENT--> [?] Cardiovascular disorders present in the perinatal or neonatal period Def: A group of conditions which begin during the period of time around childbirth, especially the five months before and one month after birth which are associated with the cardiovascular systems.... --EXCLUDES--> [?] 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.... --- Walk 6 --- [KB42] Persistent pulmonary hypertension of the newborn Def: Persistent pulmonary hypertension of the newborn is a cardiopulmonary disorder characterised by systemic arterial hypoxemia secondary to pulmonary hypertension and extrapulmonary right-to-left shuntin... --PARENT--> [?] Cardiovascular disorders present in the perinatal or neonatal period Def: A group of conditions which begin during the period of time around childbirth, especially the five months before and one month after birth which are associated with the cardiovascular systems.... --CHILD--> [KB42] Persistent pulmonary hypertension of the newborn Def: Persistent pulmonary hypertension of the newborn is a cardiopulmonary disorder characterised by systemic arterial hypoxemia secondary to pulmonary hypertension and extrapulmonary right-to-left shuntin...
[ "[MG40.Z] Shock, unspecified\n --PARENT--> [MG40] Shock\n Def: Shock is a life-threatening medical condition that occurs due to inadequate substrate for aerobic cellular respiration. In the early stages this is generally an inadequate tissue level of oxygen. Shoc...\n --CHILD--> [MG40.Y] Other specified shock", "[MG40.Z] Shock, unspecified\n --PARENT--> [MG40] Shock\n Def: Shock is a life-threatening medical condition that occurs due to inadequate substrate for aerobic cellular respiration. In the early stages this is generally an inadequate tissue level of oxygen. Shoc...\n --RELATED_TO--> [?] Shock following abortion, ectopic or molar pregnancy", "[BE2Z] Diseases of the circulatory system, unspecified\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...", "[BE2Z] Diseases of the circulatory system, unspecified\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 --RELATED_TO--> [?] Functional vascular disorders of the skin\n Def: Skin disorders due to disturbances in vascular tone and skin blood flow....", "[KB42] Persistent pulmonary hypertension of the newborn\n Def: Persistent pulmonary hypertension of the newborn is a cardiopulmonary disorder characterised by systemic arterial hypoxemia secondary to pulmonary hypertension and extrapulmonary right-to-left shuntin...\n --PARENT--> [?] Cardiovascular disorders present in the perinatal or neonatal period\n Def: A group of conditions which begin during the period of time around childbirth, especially the five months before and one month after birth which are associated with the cardiovascular systems....\n --EXCLUDES--> [?] 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....", "[KB42] Persistent pulmonary hypertension of the newborn\n Def: Persistent pulmonary hypertension of the newborn is a cardiopulmonary disorder characterised by systemic arterial hypoxemia secondary to pulmonary hypertension and extrapulmonary right-to-left shuntin...\n --PARENT--> [?] Cardiovascular disorders present in the perinatal or neonatal period\n Def: A group of conditions which begin during the period of time around childbirth, especially the five months before and one month after birth which are associated with the cardiovascular systems....\n --CHILD--> [KB42] Persistent pulmonary hypertension of the newborn\n Def: Persistent pulmonary hypertension of the newborn is a cardiopulmonary disorder characterised by systemic arterial hypoxemia secondary to pulmonary hypertension and extrapulmonary right-to-left shuntin..." ]
MG40.Z
Shock, unspecified
[ { "from_icd11": "MG40.Z", "icd10_code": "T8111XA", "icd10_title": "Postprocedural cardiogenic shock, initial encounter" }, { "from_icd11": "MG40.Z", "icd10_code": "T8112XA", "icd10_title": "Postprocedural septic shock, initial encounter" }, { "from_icd11": "MG40.Z", "icd10_code": "T882XXA", "icd10_title": "Shock due to anesthesia, initial encounter" }, { "from_icd11": "MG40.Z", "icd10_code": "T8110XA", "icd10_title": "Postprocedural shock unspecified, initial encounter" }, { "from_icd11": "MG40.Z", "icd10_code": "R579", "icd10_title": "Shock, unspecified" }, { "from_icd11": "MG40.Z", "icd10_code": "R578", "icd10_title": "Other shock" }, { "from_icd11": "MG40.Z", "icd10_code": "R57", "icd10_title": "Shock, not elsewhere classified" }, { "from_icd11": "MG40.Z", "icd10_code": "T811", "icd10_title": "Postprocedural shock" }, { "from_icd11": "MG40.Z", "icd10_code": "T882", "icd10_title": "Shock due to anesthesia" }, { "from_icd11": "BE2Z", "icd10_code": "I998", "icd10_title": "Other disorder of circulatory system" }, { "from_icd11": "BE2Z", "icd10_code": "I999", "icd10_title": "Unspecified disorder of circulatory system" }, { "from_icd11": "BE2Z", "icd10_code": "I4949", "icd10_title": "Other premature depolarization" }, { "from_icd11": "BE2Z", "icd10_code": "I4940", "icd10_title": "Unspecified premature depolarization" }, { "from_icd11": "BE2Z", "icd10_code": "I499", "icd10_title": "Cardiac arrhythmia, unspecified" }, { "from_icd11": "BE2Z", "icd10_code": "I498", "icd10_title": "Other specified cardiac arrhythmias" } ]
T8111XA
Postprocedural cardiogenic shock, initial encounter
Various cases of patients with cardiac tumors presenting with ECG changes have been reported dating back to as early as 1934 . We consider this case important to report because the patients in most of the previously documented cases presented with cardiopulmonary symptoms. For example, a case reported by Demir et al. in January 2019 described a 59-year-old man with a history of tongue cancer who presented to the emergency department for acute-onset chest pain . The ECG demonstrated ST-segment elevation in leads V1-V6 consistent with acute anterior wall myocardial infarction and the patient was found to have a large tumor involving the right ventricular free wall on TTE. Another case published by Xiang et al. in February 2020 detailed a 66-year-old man who presented to his internist’s office with nonproductive cough, lower extremity edema, and dyspnea at rest who was found to have elevation of the ST-segment in leads II, III, and aVF, as well as leads V3-V6 concerning for acute myocardial infarction . Computed tomography of the patient’s chest demonstrated anterior bulging of the left and right ventricles that was subsequently biopsied and revealed high-grade malignant spindle and epithelioid neoplasm. In contrast to these and other previously documented cases, our patient was asymptomatic from his cardiac tumor at presentation, even in the context of developing cardiac tamponade physiology on TTE.
3.994141
0.934082
sec[2]/p[1]
en
0.999996
33884235
https://doi.org/10.7759/cureus.13981
[ "cases", "cardiac", "leads", "patients", "previously", "documented", "chest", "segment", "elevation", "wall" ]
[ { "code": "JB20.Z", "title": "Single spontaneous delivery, unspecified" }, { "code": "QA48.0", "title": "Care or examination immediately after delivery" }, { "code": "BE2Y", "title": "Other specified diseases of the circulatory system" }, { "code": "BC4Z", "title": "Diseases of the myocardium or cardiac chambers, unspecified" }, { "code": "BD1Z", "title": "Heart failure, unspecified" }, { "code": "LA8Z", "title": "Structural developmental anomaly of heart or great vessels, unspecified" }, { "code": "BA41.Z", "title": "Acute myocardial infarction, unspecified" }, { "code": "NE61", "title": "Harmful effects of or exposure to noxious substances, chiefly nonmedicinal as to source, not elsewhere classified" }, { "code": "CA60.Y/PB36&XB17", "title": "Lead miner lung" }, { "code": "MA13.00", "title": "Abnormal level of lead in blood" } ]
=== ICD-11 CODES FOUND === [JB20.Z] Single spontaneous delivery, unspecified Also known as: Single spontaneous delivery, unspecified | Single spontaneous delivery | spontaneous delivery NOS | normal delivery NOS | uncomplicated delivery [QA48.0] Care or examination immediately after delivery Also known as: Care or examination immediately after delivery | care and observation in uncomplicated delivery cases | postpartum care immediately after delivery | postpartum examination immediately after delivery | Postpartum care after hospital delivery Excludes: Complications predominantly related to the puerperium [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 [BC4Z] Diseases of the myocardium or cardiac chambers, unspecified Also known as: Diseases of the myocardium or cardiac chambers, unspecified | Heart disease NOS | cardiac disease NOS [BD1Z] Heart failure, unspecified Also known as: Heart failure, unspecified | myocardial failure | cardiac decompensation | cardiac failure | cardiac failure NOS [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 [BA41.Z] Acute myocardial infarction, unspecified Also known as: Acute myocardial infarction, unspecified | Acute myocardial infarction | cardiac attack | heart attack | acute cardiac infarction [NE61] Harmful effects of or exposure to noxious substances, chiefly nonmedicinal as to source, not elsewhere classified Also known as: Harmful effects of or exposure to noxious substances, chiefly nonmedicinal as to source, not elsewhere classified | Harmful effects of or exposure to noxious substances chiefly nonmedicinal as to source, alcohols | alcohol poisoning | alcohol toxicity | Harmful effects of or exposure to noxious substances chiefly nonmedicinal as to source, Ethanol Excludes: corrosions | Bacterial foodborne intoxications [MA13.00] Abnormal level of lead in blood Definition: Abnormal level of lead in blood in those who have been exposed to lead and who require management. Also known as: Abnormal level of lead in blood Excludes: Harmful effects of or exposure to noxious substances, Substances chiefly nonmedicinal as to source, Metals === GRAPH WALKS === --- Walk 1 --- [JB20.Z] Single spontaneous delivery, unspecified --PARENT--> [JB20] Single spontaneous delivery Def: A condition caused by the development of a fetus to the culmination of the pregnancy period. This condition is characterised by spontaneous parturition of a neonate from the uterus.... --CHILD--> [JB20.1] Spontaneous breech delivery Def: A condition caused by the development of a fetus to the culmination of the pregnancy period. This condition is characterised by spontaneous parturition of a neonate in breech position from the uterus.... --- Walk 2 --- [JB20.Z] Single spontaneous delivery, unspecified --PARENT--> [JB20] Single spontaneous delivery Def: A condition caused by the development of a fetus to the culmination of the pregnancy period. This condition is characterised by spontaneous parturition of a neonate from the uterus.... --PARENT--> [?] Delivery Def: Birth of one or more neonates from the uterus either spontaneously, assisted, or by caesarean section.... --- Walk 3 --- [QA48.0] Care or examination immediately after delivery --PARENT--> [QA48] Postpartum care or examination --CHILD--> [QA48.1] Care or examination of lactating mother --- Walk 4 --- [QA48.0] Care or examination immediately after delivery --EXCLUDES--> [?] Complications predominantly related to the puerperium Def: A group of conditions characterised as any adverse evolution (complication) which may arise during the approximately six weeks after delivery during which the uterus returns to the original size (puer... --CHILD--> [?] Infections in the puerperium --- Walk 5 --- [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... --RELATED_TO--> [?] Cerebrovascular diseases Def: This is a group of brain dysfunctions related to disease of the blood vessels supplying the brain. This includes “stroke”, which includes the following entities: Intracerebral haemorrhage; Subarachnoi... --- Walk 6 --- [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--> [?] Ischaemic heart diseases
[ "[JB20.Z] Single spontaneous delivery, unspecified\n --PARENT--> [JB20] Single spontaneous delivery\n Def: A condition caused by the development of a fetus to the culmination of the pregnancy period. This condition is characterised by spontaneous parturition of a neonate from the uterus....\n --CHILD--> [JB20.1] Spontaneous breech delivery\n Def: A condition caused by the development of a fetus to the culmination of the pregnancy period. This condition is characterised by spontaneous parturition of a neonate in breech position from the uterus....", "[JB20.Z] Single spontaneous delivery, unspecified\n --PARENT--> [JB20] Single spontaneous delivery\n Def: A condition caused by the development of a fetus to the culmination of the pregnancy period. This condition is characterised by spontaneous parturition of a neonate from the uterus....\n --PARENT--> [?] Delivery\n Def: Birth of one or more neonates from the uterus either spontaneously, assisted, or by caesarean section....", "[QA48.0] Care or examination immediately after delivery\n --PARENT--> [QA48] Postpartum care or examination\n --CHILD--> [QA48.1] Care or examination of lactating mother", "[QA48.0] Care or examination immediately after delivery\n --EXCLUDES--> [?] Complications predominantly related to the puerperium\n Def: A group of conditions characterised as any adverse evolution (complication) which may arise during the approximately six weeks after delivery during which the uterus returns to the original size (puer...\n --CHILD--> [?] Infections in the puerperium", "[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 --RELATED_TO--> [?] Cerebrovascular diseases\n Def: This is a group of brain dysfunctions related to disease of the blood vessels supplying the brain. This includes “stroke”, which includes the following entities: Intracerebral haemorrhage; Subarachnoi...", "[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--> [?] Ischaemic heart diseases" ]
JB20.Z
Single spontaneous delivery, unspecified
[ { "from_icd11": "JB20.Z", "icd10_code": "O80", "icd10_title": "Encounter for full-term uncomplicated delivery" }, { "from_icd11": "JB20.Z", "icd10_code": "O808", "icd10_title": "" }, { "from_icd11": "JB20.Z", "icd10_code": "O809", "icd10_title": "" }, { "from_icd11": "QA48.0", "icd10_code": "Z390", "icd10_title": "Encounter for care and examination of mother immediately after delivery" }, { "from_icd11": "BC4Z", "icd10_code": "I5181", "icd10_title": "Takotsubo syndrome" }, { "from_icd11": "BC4Z", "icd10_code": "I5189", "icd10_title": "Other ill-defined heart diseases" }, { "from_icd11": "BC4Z", "icd10_code": "I519", "icd10_title": "Heart disease, unspecified" }, { "from_icd11": "BC4Z", "icd10_code": "I510", "icd10_title": "Cardiac septal defect, acquired" }, { "from_icd11": "BC4Z", "icd10_code": "I515", "icd10_title": "Myocardial degeneration" }, { "from_icd11": "BC4Z", "icd10_code": "I51", "icd10_title": "Complications and ill-defined descriptions of heart disease" }, { "from_icd11": "BC4Z", "icd10_code": "I516", "icd10_title": "" }, { "from_icd11": "BC4Z", "icd10_code": "I518", "icd10_title": "Other ill-defined heart diseases" }, { "from_icd11": "BD1Z", "icd10_code": "I5023", "icd10_title": "Acute on chronic systolic (congestive) heart failure" }, { "from_icd11": "BD1Z", "icd10_code": "I5030", "icd10_title": "Unspecified diastolic (congestive) heart failure" }, { "from_icd11": "BD1Z", "icd10_code": "I5031", "icd10_title": "Acute diastolic (congestive) heart failure" } ]
O80
Encounter for full-term uncomplicated delivery
Endoscopic ultrasound with aspiration collected 0.4-mL blood-tinged, thick and viscous fluid and scattered debris. Molecular testing returned as negative; however, gene fusion studies and molecular interpretations were equivocal. MRI confirmed the mass but raised questions about splenic vessel abutment . A subsequent CT dual pancreas confirmed splenic vessel abutment; although the mass did come close to the left adrenal gland, it did not appear that it stemmed from the organ . Repeat endoscopic ultrasound showed a mass measuring 6.8 × 2.8-cm mass in the upper abdomen/perigastric region inseparable from the pancreatic tail . The origin of the mass was indeterminate; however, given its appearance and how it was inseparable and exophytic from the pancreatic body extending into the tail, it maintains a strong possibility that it was pancreatic in origin. Ultimately, through collections of spindle cells and ganglion cells, both of which by immunochemistry tested positive for synaptophysin, S100 protein, and neurofilament stain, biopsy results confirmed a final diagnosis of GN . Although the mass appeared benign without any compressive effects, its large size warranted a thorough pathological assessment. Therefore, a left pancreatectomy and splenectomy (with appropriate vaccinations before surgery) was recommended. The patient was referred to surgery and is still pending surgical evaluation to this day.
4.039063
0.974609
sec[1]/p[1]
en
0.999996
40242301
https://doi.org/10.14309/crj.0000000000001677
[ "pancreatic", "endoscopic", "ultrasound", "molecular", "however", "splenic", "vessel", "abutment", "although", "that" ]
[ { "code": "DC3Z", "title": "Diseases of pancreas, unspecified" }, { "code": "DC3Y", "title": "Other specified diseases of pancreas" }, { "code": "LB21.3", "title": "Agenesis-aplasia of pancreas" }, { "code": "LB21.Z", "title": "Structural developmental anomalies of pancreas, unspecified" }, { "code": "DC35.0", "title": "Atrophy of pancreas" }, { "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 === [DC3Z] Diseases of pancreas, unspecified Also known as: Diseases of pancreas, unspecified [DC3Y] Other specified diseases of pancreas Also known as: Other specified diseases of pancreas | Calculus of pancreas | pancreas calculi | pancreas duct calculus | pancreas duct lithiasis [LB21.3] Agenesis-aplasia of pancreas Definition: This refers to the failure of an organ to develop during embryonic growth and development due to the absence of primordial tissue of the pancreas. Also known as: Agenesis-aplasia of pancreas | Congenital absence of pancreas | Congenital pancreas absence | Congenital pancreatic absence | Absent pancreas [LB21.Z] Structural developmental anomalies of pancreas, unspecified Also known as: Structural developmental anomalies of pancreas, unspecified | Structural developmental anomalies of pancreas | malformations of pancreas | anomalies of pancreas | congenital abnormality of pancreas [DC35.0] Atrophy of pancreas Also known as: Atrophy of pancreas | pancreatic atrophy | pancreas ductal atrophy [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 --- [DC3Z] Diseases of pancreas, unspecified --PARENT--> [?] Diseases of pancreas Def: This is a group of conditions characterised as being in or associated with the pancreas.... --PARENT--> [13] Diseases of the digestive system --- Walk 2 --- [DC3Z] Diseases of pancreas, unspecified --PARENT--> [?] Diseases of pancreas Def: This is a group of conditions characterised as being in or associated with the pancreas.... --CHILD--> [DC31] Acute pancreatitis Def: Inflammation of the pancreas with sudden onset. Pathological changes range from oedema to necrosis. While mild cases often recover without complications, severe cases have high mortality due to system... --- Walk 3 --- [DC3Y] Other specified diseases of pancreas --PARENT--> [?] Diseases of pancreas Def: This is a group of conditions characterised as being in or associated with the pancreas.... --RELATED_TO--> [?] Structural developmental anomalies of pancreas --- Walk 4 --- [DC3Y] Other specified diseases of pancreas --PARENT--> [?] Diseases of pancreas Def: This is a group of conditions characterised as being in or associated with the pancreas.... --RELATED_TO--> [?] Structural developmental anomalies of pancreas --- Walk 5 --- [LB21.3] Agenesis-aplasia of pancreas Def: This refers to the failure of an organ to develop during embryonic growth and development due to the absence of primordial tissue of the pancreas.... --PARENT--> [LB21] Structural developmental anomalies of pancreas --CHILD--> [LB21.0] Annular pancreas Def: Annular pancreas is a distinct form of duodenal atresia in which the head of the pancreas forms a ring around the second portion of the duodenum. During the neonatal period, the clinical picture is do... --- Walk 6 --- [LB21.3] Agenesis-aplasia of pancreas Def: This refers to the failure of an organ to develop during embryonic growth and development due to the absence of primordial tissue of the pancreas.... --PARENT--> [LB21] Structural developmental anomalies of pancreas --CHILD--> [LB21.1] Pancreas divisum Def: This is a congenital anomaly in the anatomy of the ducts of the pancreas in which a single pancreatic duct is not formed, but rather remains as two distinct dorsal and ventral ducts....
[ "[DC3Z] Diseases of pancreas, unspecified\n --PARENT--> [?] Diseases of pancreas\n Def: This is a group of conditions characterised as being in or associated with the pancreas....\n --PARENT--> [13] Diseases of the digestive system", "[DC3Z] Diseases of pancreas, unspecified\n --PARENT--> [?] Diseases of pancreas\n Def: This is a group of conditions characterised as being in or associated with the pancreas....\n --CHILD--> [DC31] Acute pancreatitis\n Def: Inflammation of the pancreas with sudden onset. Pathological changes range from oedema to necrosis. While mild cases often recover without complications, severe cases have high mortality due to system...", "[DC3Y] Other specified diseases of pancreas\n --PARENT--> [?] Diseases of pancreas\n Def: This is a group of conditions characterised as being in or associated with the pancreas....\n --RELATED_TO--> [?] Structural developmental anomalies of pancreas", "[DC3Y] Other specified diseases of pancreas\n --PARENT--> [?] Diseases of pancreas\n Def: This is a group of conditions characterised as being in or associated with the pancreas....\n --RELATED_TO--> [?] Structural developmental anomalies of pancreas", "[LB21.3] Agenesis-aplasia of pancreas\n Def: This refers to the failure of an organ to develop during embryonic growth and development due to the absence of primordial tissue of the pancreas....\n --PARENT--> [LB21] Structural developmental anomalies of pancreas\n --CHILD--> [LB21.0] Annular pancreas\n Def: Annular pancreas is a distinct form of duodenal atresia in which the head of the pancreas forms a ring around the second portion of the duodenum. During the neonatal period, the clinical picture is do...", "[LB21.3] Agenesis-aplasia of pancreas\n Def: This refers to the failure of an organ to develop during embryonic growth and development due to the absence of primordial tissue of the pancreas....\n --PARENT--> [LB21] Structural developmental anomalies of pancreas\n --CHILD--> [LB21.1] Pancreas divisum\n Def: This is a congenital anomaly in the anatomy of the ducts of the pancreas in which a single pancreatic duct is not formed, but rather remains as two distinct dorsal and ventral ducts...." ]
DC3Z
Diseases of pancreas, unspecified
[ { "from_icd11": "DC3Z", "icd10_code": "K8681", "icd10_title": "Exocrine pancreatic insufficiency" }, { "from_icd11": "DC3Z", "icd10_code": "K8689", "icd10_title": "Other specified diseases of pancreas" }, { "from_icd11": "DC3Z", "icd10_code": "K869", "icd10_title": "Disease of pancreas, unspecified" }, { "from_icd11": "DC3Z", "icd10_code": "K868", "icd10_title": "Other specified diseases of pancreas" }, { "from_icd11": "DC3Z", "icd10_code": "K87", "icd10_title": "Disorders of gallbladder, biliary tract and pancreas in diseases classified elsewhere" }, { "from_icd11": "DC3Z", "icd10_code": "K80-K87", "icd10_title": "" }, { "from_icd11": "DC3Z", "icd10_code": "K86", "icd10_title": "Other diseases of pancreas" }, { "from_icd11": "DC3Z", "icd10_code": "K871", "icd10_title": "" }, { "from_icd11": "LB21.Z", "icd10_code": "Q450", "icd10_title": "Agenesis, aplasia and hypoplasia of pancreas" }, { "from_icd11": "LB21.Z", "icd10_code": "Q38-Q45", "icd10_title": "" }, { "from_icd11": "LB21.Z", "icd10_code": "Q45", "icd10_title": "Other congenital malformations of digestive system" }, { "from_icd11": "LB21.Z", "icd10_code": "Q452", "icd10_title": "Congenital pancreatic cyst" }, { "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" } ]
K8681
Exocrine pancreatic insufficiency
Diagnosis of this patient at 5 months of age was based on hallmarks of CHARGE, including choanal atresia, multiple heart defects, genitourinary abnormalities, and triangular conchae of the ear. Each of these findings on its own is relatively rare, and when seen together become highly specific for CHARGE. In addition, the patient received the available genetic workup procedures at the time, for example, to rigorously rule out DiGeorge Syndrome, a more prevalent disorder that shares some clinical features with CHARGE. Fluorescent in situ hybridization studies were negative for the 22q11.2 locus for DiGeorge Syndrome, as were chromosomal analyses for genetic defects. We attempted DNA extraction from formalin fixed paraffin embedded tissue from this patient in order to perform sequence analysis of the CHD7 gene; however, we were unable to do so as the tissue is 24.5 years old, and the DNA is likely degraded. On gross pathologic examination, multiple practicing neuropathologists observed frank polymicrogyria of the left middle lobe, including both the biventral and inferior semilunar lobules. Given the clear diagnosis of CHARGE and that an estimated 67–90% of CHARGE patients have mutations in CHD7 14 , 72 , 73 , we report this case as a relevant initial finding, and propose that analyses of postmortem brain tissue from CHD7 mutant CHARGE patients by investigators with access to the tissue is warranted.
4.183594
0.621582
sec[3]/sec[12]/p[0]
en
0.999996
34588434
https://doi.org/10.1038/s41467-021-25846-3
[ "charge", "tissue", "this", "that", "including", "multiple", "defects", "genetic", "digeorge", "analyses" ]
[ { "code": "5A61.0", "title": "Hypopituitarism" }, { "code": "PJ60", "title": "Explosion of depth-charge or marine mine during armed conflict" }, { "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": "4A01.03", "title": "Transient hypogammaglobulinaemia of infancy" }, { "code": "8A80.Z", "title": "Migraine, unspecified" }, { "code": "QA76", "title": "Medication or substance that is known to be an allergen without injury or harm" } ]
=== ICD-11 CODES FOUND === [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 [PJ60] Explosion of depth-charge or marine mine during armed conflict Also known as: Explosion of depth-charge or marine mine during armed conflict [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 [4A01.03] Transient hypogammaglobulinaemia of infancy Also known as: Transient hypogammaglobulinaemia of infancy | immunoglobulin maturational delay | THI - [transient hypogammaglobulinaemia of infancy] [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 === GRAPH WALKS === --- Walk 1 --- [5A61.0] Hypopituitarism Def: A disorder manifesting a deficiency or decrease of one or more pituitary hormones, which is caused by a variety of diseases such as tumour, trauma/surgery, irradiation, inflammation and haemorrhage/in... --RELATED_TO--> [?] Argonz-del Castillo Syndrome --PARENT--> [?] Functional hyperprolactinoma Def: Increased blood level of prolactin caused by non-tumourous mechanisms such as disruption of pituitary stalk, severe hypothyroidism, or administration of dopamine receptor antagonists.... --- Walk 2 --- [5A61.0] Hypopituitarism Def: A disorder manifesting a deficiency or decrease of one or more pituitary hormones, which is caused by a variety of diseases such as tumour, trauma/surgery, irradiation, inflammation and haemorrhage/in... --PARENT--> [5A61] Hypofunction or certain other specified disorders of pituitary gland Def: Clinical status with disordered function of the pituitary gland without excessive pituitary hormone production, which is caused by a variety of diseases... --EXCLUDES--> [?] Primary neoplasms of brain --- Walk 3 --- [PJ60] Explosion of depth-charge or marine mine during armed conflict --PARENT--> [?] Explosion of marine weapons during armed conflict --CHILD--> [PJ60] Explosion of depth-charge or marine mine during armed conflict --- Walk 4 --- [PJ60] Explosion of depth-charge or marine mine during armed conflict --PARENT--> [?] Explosion of marine weapons during armed conflict --CHILD--> [PJ60] Explosion of depth-charge or marine mine during armed conflict --- Walk 5 --- [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 6 --- [FB6Z] Soft tissue disorders, unspecified --PARENT--> [?] Soft tissue disorders --RELATED_TO--> [?] Diabetic radiculoplexoneuropathy Def: Diabetic radiculoplexoneuropathy is a rare, but established complication of a focal neuropathy occurring in patients with diabetes type 2. Etiologically inflammatory changes of microvasculitis are ass...
[ "[5A61.0] Hypopituitarism\n Def: A disorder manifesting a deficiency or decrease of one or more pituitary hormones, which is caused by a variety of diseases such as tumour, trauma/surgery, irradiation, inflammation and haemorrhage/in...\n --RELATED_TO--> [?] Argonz-del Castillo Syndrome\n --PARENT--> [?] Functional hyperprolactinoma\n Def: Increased blood level of prolactin caused by non-tumourous mechanisms such as disruption of pituitary stalk, severe hypothyroidism, or administration of dopamine receptor antagonists....", "[5A61.0] Hypopituitarism\n Def: A disorder manifesting a deficiency or decrease of one or more pituitary hormones, which is caused by a variety of diseases such as tumour, trauma/surgery, irradiation, inflammation and haemorrhage/in...\n --PARENT--> [5A61] Hypofunction or certain other specified disorders of pituitary gland\n Def: Clinical status with disordered function of the pituitary gland without excessive pituitary hormone production, which is caused by a variety of diseases...\n --EXCLUDES--> [?] Primary neoplasms of brain", "[PJ60] Explosion of depth-charge or marine mine during armed conflict\n --PARENT--> [?] Explosion of marine weapons during armed conflict\n --CHILD--> [PJ60] Explosion of depth-charge or marine mine during armed conflict", "[PJ60] Explosion of depth-charge or marine mine during armed conflict\n --PARENT--> [?] Explosion of marine weapons during armed conflict\n --CHILD--> [PJ60] Explosion of depth-charge or marine mine during armed conflict", "[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....", "[FB6Z] Soft tissue disorders, unspecified\n --PARENT--> [?] Soft tissue disorders\n --RELATED_TO--> [?] Diabetic radiculoplexoneuropathy\n Def: Diabetic radiculoplexoneuropathy is a rare, but established complication of a focal neuropathy occurring in patients with diabetes type 2. Etiologically inflammatory changes of microvasculitis are ass..." ]
5A61.0
Hypopituitarism
[ { "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": "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" } ]
E230
Hypopituitarism
Therapeutic intervention: the treatment plan for this patient was endodontic intervention for upper left central incisor (UL1) followed by elimination of periodontal inflammation by regenerative periodontal surgery. After subgingival scaling and root planning, oral hygiene instructions were given. Occlusal interferences were checked, and occlusal adjustment was performed to prevent trauma from occlusion. One month later, although the clinical signs of gingival inflammation had disappeared, a deep pocket was left in relation to the treated tooth. According to the treatment plan, regenerative periodontal therapy using GeistlichBio-Oss® was performed. Following local anesthesia, horizontal and vertical releasing incisions were performed. A full-thickness flap was elevated. The defect was completely debrided, and the surfaces were carefully scaled and planed . The defect was treated with bone graft material . The flap was then sutured and packed with Coe-Pak™. Post-surgical standard antibiotics' regimen was prescribed to the patient. The suture removal was done after one week of the surgery. The patient was kept on maintenance therapy at 1-2 months´ interval for six months. It was observed that after this stipulated time of six months, diastema was completely closed . At this appointment, full-mouth professional prophylaxis and a fiber reinforced splint was given to maintain the position of the tooth.
3.802734
0.978027
sec[1]/p[3]
en
0.999997
PMC8956899
https://doi.org/10.11604/pamj.2022.41.39.29953
[ "this", "periodontal", "intervention", "plan", "inflammation", "regenerative", "occlusal", "treated", "tooth", "full" ]
[ { "code": "4A01.03", "title": "Transient hypogammaglobulinaemia of infancy" }, { "code": "DA0C.Y", "title": "Other specified periodontal disease" }, { "code": "DA0C.Z", "title": "Periodontal disease, unspecified" }, { "code": "DA0C.0", "title": "Acute periodontitis" }, { "code": "DA0C.1", "title": "Aggressive periodontitis" }, { "code": "DA09.71", "title": "Chronic apical periodontitis" }, { "code": "PL11.2Z", "title": "Embolisation, as mode of injury or harm, unspecified" }, { "code": "PJ46", "title": "Legal intervention involving gas" }, { "code": "PJ4Z", "title": "Legal intervention involving unspecified means" }, { "code": "PJ45", "title": "Legal intervention involving explosive" } ]
=== ICD-11 CODES FOUND === [4A01.03] Transient hypogammaglobulinaemia of infancy Also known as: Transient hypogammaglobulinaemia of infancy | immunoglobulin maturational delay | THI - [transient hypogammaglobulinaemia of infancy] [DA0C.Y] Other specified periodontal disease Also known as: Other specified periodontal disease | Chronic periodontitis | Adult periodontitis | adult-onset periodontitis | chronic pericementitis [DA0C.Z] Periodontal disease, unspecified Also known as: Periodontal disease, unspecified | Periodontal disease [DA0C.0] Acute periodontitis Definition: This is an acute disease affecting the tooth-supporting structures, i.e. gingiva, alveolar bone and periodontal membrane. Also known as: Acute periodontitis | acute pericementitis | aggressive and acute periodontitis | peridental infection | periodontal infection Excludes: Periapical abscess without sinus | Acute apical periodontitis of pulpal origin | Periapical abscess with sinus [DA0C.1] Aggressive periodontitis Definition: A type of periodontal disease and includes localised aggressive periodontitis (LAP), and Generalised aggressive periodontitis (GAP). Also known as: Aggressive periodontitis | Juvenile periodontitis | prepubertal periodontitis | Generalised aggressive periodontitis | Localised aggresssive periodontitis Includes: Juvenile periodontitis [DA09.71] Chronic apical periodontitis Definition: A periapical inflammation characterised by dental granuloma formation. Also known as: Chronic apical periodontitis | Apical periodontitis NOS | apex periodontitis | periapical infection NOS | Apical or periapical granuloma [PL11.2Z] Embolisation, as mode of injury or harm, unspecified Also known as: Embolisation, as mode of injury or harm, unspecified | Embolisation, as mode of injury or harm | embolic phenomenon as mode of injury | embolism due to intervention | injection of air as mode of injury [PJ46] Legal intervention involving gas Also known as: Legal intervention involving gas | Asphyxiation by gas due to legal intervention | Injury by tear gas due to legal intervention | Poisoning by gas due to legal intervention [PJ4Z] Legal intervention involving unspecified means Also known as: Legal intervention involving unspecified means [PJ45] Legal intervention involving explosive Also known as: Legal intervention involving explosive | Legal intervention involving dynamite | Legal intervention involving explosive shell | Legal intervention involving grenade | Legal intervention involving mortar bomb === GRAPH WALKS === --- Walk 1 --- [4A01.03] Transient hypogammaglobulinaemia of infancy --PARENT--> [4A01.0] Immunodeficiencies with predominantly antibody defects Def: A disorder characterised by an inability to mount a normal immune response due to antibody (i.e. immunoglobulin) defects... --CHILD--> [4A01.00] Hereditary agammaglobulinaemia with profoundly reduced or absent B cells Def: This refers to a hereditary type of primary immune deficiency disease characterised by a reduction in all types of gamma globulins, and rare X-linked genetic disorder that affects the body's ability t... --- Walk 2 --- [4A01.03] Transient hypogammaglobulinaemia of infancy --PARENT--> [4A01.0] Immunodeficiencies with predominantly antibody defects Def: A disorder characterised by an inability to mount a normal immune response due to antibody (i.e. immunoglobulin) defects... --CHILD--> [4A01.02] Specific antibody deficiency with normal immunoglobulin concentrations or normal number of B cells --- Walk 3 --- [DA0C.Y] Other specified periodontal disease --PARENT--> [DA0C] Periodontal disease Def: Periodontal disease can refer to any pathological process involving the gum (GINGIVA), the alveolar bone (alveolar process), the dental cementum, and / or the periodontal ligament... --PARENT--> [?] Diseases or disorders of orofacial complex Def: Morbid process, derangement or abnormality localised in the mouth or related tissues of the face... --- Walk 4 --- [DA0C.Y] Other specified periodontal disease --PARENT--> [DA0C] Periodontal disease Def: Periodontal disease can refer to any pathological process involving the gum (GINGIVA), the alveolar bone (alveolar process), the dental cementum, and / or the periodontal ligament... --CHILD--> [DA0C.1] Aggressive periodontitis Def: A type of periodontal disease and includes localised aggressive periodontitis (LAP), and Generalised aggressive periodontitis (GAP).... --- Walk 5 --- [DA0C.Z] Periodontal disease, unspecified --PARENT--> [DA0C] Periodontal disease Def: Periodontal disease can refer to any pathological process involving the gum (GINGIVA), the alveolar bone (alveolar process), the dental cementum, and / or the periodontal ligament... --CHILD--> [DA0C.0] Acute periodontitis Def: This is an acute disease affecting the tooth-supporting structures, i.e. gingiva, alveolar bone and periodontal membrane.... --- Walk 6 --- [DA0C.Z] Periodontal disease, unspecified --PARENT--> [DA0C] Periodontal disease Def: Periodontal disease can refer to any pathological process involving the gum (GINGIVA), the alveolar bone (alveolar process), the dental cementum, and / or the periodontal ligament... --CHILD--> [DA0C.2] Periodontosis Def: Periodontosis defined as a disease of the periodontium occurring in an otherwise healthy adolescent and characterised by a rapid loss of the alveolar bone around more than one tooth of the permanent d...
[ "[4A01.03] Transient hypogammaglobulinaemia of infancy\n --PARENT--> [4A01.0] Immunodeficiencies with predominantly antibody defects\n Def: A disorder characterised by an inability to mount a normal immune response due to antibody (i.e. immunoglobulin) defects...\n --CHILD--> [4A01.00] Hereditary agammaglobulinaemia with profoundly reduced or absent B cells\n Def: This refers to a hereditary type of primary immune deficiency disease characterised by a reduction in all types of gamma globulins, and rare X-linked genetic disorder that affects the body's ability t...", "[4A01.03] Transient hypogammaglobulinaemia of infancy\n --PARENT--> [4A01.0] Immunodeficiencies with predominantly antibody defects\n Def: A disorder characterised by an inability to mount a normal immune response due to antibody (i.e. immunoglobulin) defects...\n --CHILD--> [4A01.02] Specific antibody deficiency with normal immunoglobulin concentrations or normal number of B cells", "[DA0C.Y] Other specified periodontal disease\n --PARENT--> [DA0C] Periodontal disease\n Def: Periodontal disease can refer to any pathological process involving the gum (GINGIVA), the alveolar bone (alveolar process), the dental cementum, and / or the periodontal ligament...\n --PARENT--> [?] Diseases or disorders of orofacial complex\n Def: Morbid process, derangement or abnormality localised in the mouth or related tissues of the face...", "[DA0C.Y] Other specified periodontal disease\n --PARENT--> [DA0C] Periodontal disease\n Def: Periodontal disease can refer to any pathological process involving the gum (GINGIVA), the alveolar bone (alveolar process), the dental cementum, and / or the periodontal ligament...\n --CHILD--> [DA0C.1] Aggressive periodontitis\n Def: A type of periodontal disease and includes localised aggressive periodontitis (LAP), and Generalised aggressive periodontitis (GAP)....", "[DA0C.Z] Periodontal disease, unspecified\n --PARENT--> [DA0C] Periodontal disease\n Def: Periodontal disease can refer to any pathological process involving the gum (GINGIVA), the alveolar bone (alveolar process), the dental cementum, and / or the periodontal ligament...\n --CHILD--> [DA0C.0] Acute periodontitis\n Def: This is an acute disease affecting the tooth-supporting structures, i.e. gingiva, alveolar bone and periodontal membrane....", "[DA0C.Z] Periodontal disease, unspecified\n --PARENT--> [DA0C] Periodontal disease\n Def: Periodontal disease can refer to any pathological process involving the gum (GINGIVA), the alveolar bone (alveolar process), the dental cementum, and / or the periodontal ligament...\n --CHILD--> [DA0C.2] Periodontosis\n Def: Periodontosis defined as a disease of the periodontium occurring in an otherwise healthy adolescent and characterised by a rapid loss of the alveolar bone around more than one tooth of the permanent d..." ]
4A01.03
Transient hypogammaglobulinaemia of infancy
[ { "from_icd11": "4A01.03", "icd10_code": "D807", "icd10_title": "Transient hypogammaglobulinemia of infancy" }, { "from_icd11": "DA0C.Z", "icd10_code": "K0530", "icd10_title": "Chronic periodontitis, unspecified" }, { "from_icd11": "DA0C.Z", "icd10_code": "K05319", "icd10_title": "Chronic periodontitis, localized, unspecified severity" }, { "from_icd11": "DA0C.Z", "icd10_code": "K05329", "icd10_title": "Chronic periodontitis, generalized, unspecified severity" }, { "from_icd11": "DA0C.Z", "icd10_code": "K0532", "icd10_title": "Chronic periodontitis, generalized" }, { "from_icd11": "DA0C.Z", "icd10_code": "K056", "icd10_title": "Periodontal disease, unspecified" }, { "from_icd11": "DA0C.Z", "icd10_code": "K055", "icd10_title": "Other periodontal diseases" }, { "from_icd11": "DA0C.Z", "icd10_code": "K05", "icd10_title": "Gingivitis and periodontal diseases" }, { "from_icd11": "DA0C.Z", "icd10_code": "K053", "icd10_title": "Chronic periodontitis" }, { "from_icd11": "DA0C.0", "icd10_code": "K05219", "icd10_title": "Aggressive periodontitis, localized, unspecified severity" }, { "from_icd11": "DA0C.0", "icd10_code": "K0520", "icd10_title": "Aggressive periodontitis, unspecified" }, { "from_icd11": "DA0C.0", "icd10_code": "K0521", "icd10_title": "Aggressive periodontitis, localized" }, { "from_icd11": "DA0C.0", "icd10_code": "K052", "icd10_title": "Aggressive periodontitis" }, { "from_icd11": "DA09.71", "icd10_code": "K045", "icd10_title": "Chronic apical periodontitis" }, { "from_icd11": "PJ46", "icd10_code": "Y35203S", "icd10_title": "Legal intervention involving unspecified gas, suspect injured, sequela" } ]
D807
Transient hypogammaglobulinemia of infancy
Patient 3 (male; age: 59), from the Shandong Province, China, had a dry cough when smelling a pungent odor or cold air every year. Chest CT revealed the presence of a subpleural mesh shadow and ground-glass opacity in both lungs, which led to an interstitial pneumonia diagnosis . White blood cell count and ESR were normal. Given the negative results, additional tests were performed to assess the etiology of the symptoms, which included culture analysis and testing for presence of Mycoplasma pneumoniae , Chlamydia pneumoniae infection, galactomannan, and tuberculosis in BALF samples. In addition, the patient was positive (1:100) for anti-endothelial cell antibodies, representing a risk for the development of connective tissue disease in the future. Percentages of neutrophils, eosinophils, macrophages, and lymphocytes were 3.5, 1.5, 88, and 7%, respectively. Positive results were obtained using Masson’s trichrome staining of TBLB specimens. Nanopore sequencing was performed to investigate the cause of the disease; T. whipplei was the most abundant species (reads: 285), followed by Pseudomonas poae (reads: 15) and Streptococcus pseudopneumoniae (reads: 8). These results were subsequently confirmed via qPCR using two pairs of primers ( Table 1 ). The patient was treated without antibiotics and was discharged when the sequencing results were obtained; no further medical record was obtained to this day.
3.978516
0.957031
sec[2]/sec[0]/p[2]
en
0.999998
34912314
https://doi.org/10.3389/fmicb.2021.760696
[ "reads", "presence", "which", "cell", "pneumoniae", "using", "sequencing", "shandong", "province", "china" ]
[ { "code": "MB4B.0", "title": "Dyslexia and alexia" }, { "code": "6A03.0", "title": "Developmental learning disorder with impairment in reading" }, { "code": "MC80.1", "title": "Nonspecific low blood-pressure reading" }, { "code": "8A61.40", "title": "Reflex epilepsies" }, { "code": "9D93", "title": "Complex vision-related dysfunctions" }, { "code": "QB61.4", "title": "Presence of colostomy" }, { "code": "QB61.0", "title": "Presence of tracheostomy" }, { "code": "QB61.3Z", "title": "Presence of enterostomy, unspecified" }, { "code": "QB61.30", "title": "Presence of ileostomy" }, { "code": "QB61.5", "title": "Presence of cystostomy" } ]
=== ICD-11 CODES FOUND === [MB4B.0] Dyslexia and alexia Definition: Dyslexia and alexia refer to the loss, usually in adulthood, of a previous ability to read fluently and to accurately comprehend written material that is inconsistent with general level of intellectual functioning and is acquired after the developmental period in individuals who had previously attained these skills, such as due to a stroke or other brain injury. Also known as: Dyslexia and alexia | reading disorder | visual amnesia | aphemesthesia | Dyslexia Excludes: Developmental learning disorder [6A03.0] Developmental learning disorder with impairment in reading Definition: Developmental learning disorder with impairment in reading is characterised by significant and persistent difficulties in learning academic skills related to reading, such as word reading accuracy, reading fluency, and reading comprehension. The individual’s performance in reading is markedly below what would be expected for chronological age and level of intellectual functioning and results in significant impairment in the individual’s academic or occupational functioning. Developmental learnin Also known as: Developmental learning disorder with impairment in reading | specific reading disorder | reading disability | Specific learning disorder with impairment in reading | developmental disorder of reading Excludes: Disorders of intellectual development [MC80.1] Nonspecific low blood-pressure reading Also known as: Nonspecific low blood-pressure reading | low blood pressure reading | incidental reading of low blood pressure, without diagnosis of hypotension | incidental hyposystolic pressure reading, without diagnosis of hypotension Excludes: Maternal hypotension syndrome | Orthostatic hypotension [8A61.40] Reflex epilepsies Definition: Reflex epilepsies are rare epileptic syndromes with seizures induced by specific triggering factors (either by visual, auditory, somato-sensitive or somato-motor stimulation, or by higher cortical function activities). Photosensitive epilepsies are the most frequent form. Spontaneous seizures may also occur. "Reflex seizures'" can be classified into a simple "pure" reflex epilepsy and a complex group. The former comprises seizure triggered by simple sensory stimuli or by movements (photosensitiv Also known as: Reflex epilepsies | Photosensitive epilepsy | Reading epilepsy | Hot water epilepsy | Startle epilepsy [9D93] Complex vision-related dysfunctions Definition: Complex Vision-Related Dysfunctions involve interactions with other sensory and motor systems. They reflect the combined effects at all stages of processing. Also known as: Complex vision-related dysfunctions | Dysfunction of visual reading ability | Moderate limitation in reading ability | Profound limitation in reading ability | Dysfunctions of orientation or mobility [QB61.4] Presence of colostomy Also known as: Presence of colostomy | colon stoma status | colostomy status [QB61.0] Presence of tracheostomy Also known as: Presence of tracheostomy | trachea stoma status | tracheostomy status [QB61.3Z] Presence of enterostomy, unspecified Also known as: Presence of enterostomy, unspecified | Presence of enterostomy [QB61.30] Presence of ileostomy Also known as: Presence of ileostomy | ileum artificial opening status | ileum stoma status | ileostomy status [QB61.5] Presence of cystostomy Also known as: Presence of cystostomy | bladder stoma status | artificial opening status of bladder | cystostomy status === GRAPH WALKS === --- Walk 1 --- [MB4B.0] Dyslexia and alexia Def: Dyslexia and alexia refer to the loss, usually in adulthood, of a previous ability to read fluently and to accurately comprehend written material that is inconsistent with general level of intellectua... --EXCLUDES--> [?] Developmental learning disorder Def: Developmental learning disorder is characterised by significant and persistent difficulties in learning academic skills, which may include reading, writing, or arithmetic. The individual’s performance... --CHILD--> [?] Developmental learning disorder with impairment in reading Def: Developmental learning disorder with impairment in reading is characterised by significant and persistent difficulties in learning academic skills related to reading, such as word reading accuracy, re... --- Walk 2 --- [MB4B.0] Dyslexia and alexia Def: Dyslexia and alexia refer to the loss, usually in adulthood, of a previous ability to read fluently and to accurately comprehend written material that is inconsistent with general level of intellectua... --EXCLUDES--> [?] Developmental learning disorder Def: Developmental learning disorder is characterised by significant and persistent difficulties in learning academic skills, which may include reading, writing, or arithmetic. The individual’s performance... --CHILD--> [?] Developmental learning disorder with impairment in reading Def: Developmental learning disorder with impairment in reading is characterised by significant and persistent difficulties in learning academic skills related to reading, such as word reading accuracy, re... --- Walk 3 --- [6A03.0] Developmental learning disorder with impairment in reading Def: Developmental learning disorder with impairment in reading is characterised by significant and persistent difficulties in learning academic skills related to reading, such as word reading accuracy, re... --EXCLUDES--> [?] Disorders of intellectual development Def: Disorders of intellectual development are a group of etiologically diverse conditions originating during the developmental period characterised by significantly below average intellectual functioning ... --CHILD--> [?] Disorder of intellectual development, severe Def: A severe disorder of intellectual development is a condition originating during the developmental period characterised by significantly below average intellectual functioning and adaptive behaviour th... --- Walk 4 --- [6A03.0] Developmental learning disorder with impairment in reading Def: Developmental learning disorder with impairment in reading is characterised by significant and persistent difficulties in learning academic skills related to reading, such as word reading accuracy, re... --EXCLUDES--> [?] Disorders of intellectual development Def: Disorders of intellectual development are a group of etiologically diverse conditions originating during the developmental period characterised by significantly below average intellectual functioning ... --CHILD--> [?] Disorder of intellectual development, mild Def: A mild disorder of intellectual development is a condition originating during the developmental period characterised by significantly below average intellectual functioning and adaptive behaviour that... --- Walk 5 --- [MC80.1] Nonspecific low blood-pressure reading --EXCLUDES--> [?] Maternal hypotension syndrome Def: Any reason for encounter to assess a mother for low blood pressure during pregnancy.... --PARENT--> [?] Maternal care for other conditions predominantly related to pregnancy Def: Any reason for encounter to assess (or care for) a mother for other conditions predominantly related to pregnancy.... --- Walk 6 --- [MC80.1] Nonspecific low blood-pressure reading --EXCLUDES--> [?] Maternal hypotension syndrome Def: Any reason for encounter to assess a mother for low blood pressure during pregnancy.... --PARENT--> [?] Maternal care for other conditions predominantly related to pregnancy Def: Any reason for encounter to assess (or care for) a mother for other conditions predominantly related to pregnancy....
[ "[MB4B.0] Dyslexia and alexia\n Def: Dyslexia and alexia refer to the loss, usually in adulthood, of a previous ability to read fluently and to accurately comprehend written material that is inconsistent with general level of intellectua...\n --EXCLUDES--> [?] Developmental learning disorder\n Def: Developmental learning disorder is characterised by significant and persistent difficulties in learning academic skills, which may include reading, writing, or arithmetic. The individual’s performance...\n --CHILD--> [?] Developmental learning disorder with impairment in reading\n Def: Developmental learning disorder with impairment in reading is characterised by significant and persistent difficulties in learning academic skills related to reading, such as word reading accuracy, re...", "[MB4B.0] Dyslexia and alexia\n Def: Dyslexia and alexia refer to the loss, usually in adulthood, of a previous ability to read fluently and to accurately comprehend written material that is inconsistent with general level of intellectua...\n --EXCLUDES--> [?] Developmental learning disorder\n Def: Developmental learning disorder is characterised by significant and persistent difficulties in learning academic skills, which may include reading, writing, or arithmetic. The individual’s performance...\n --CHILD--> [?] Developmental learning disorder with impairment in reading\n Def: Developmental learning disorder with impairment in reading is characterised by significant and persistent difficulties in learning academic skills related to reading, such as word reading accuracy, re...", "[6A03.0] Developmental learning disorder with impairment in reading\n Def: Developmental learning disorder with impairment in reading is characterised by significant and persistent difficulties in learning academic skills related to reading, such as word reading accuracy, re...\n --EXCLUDES--> [?] Disorders of intellectual development\n Def: Disorders of intellectual development are a group of etiologically diverse conditions originating during the developmental period characterised by significantly below average intellectual functioning ...\n --CHILD--> [?] Disorder of intellectual development, severe\n Def: A severe disorder of intellectual development is a condition originating during the developmental period characterised by significantly below average intellectual functioning and adaptive behaviour th...", "[6A03.0] Developmental learning disorder with impairment in reading\n Def: Developmental learning disorder with impairment in reading is characterised by significant and persistent difficulties in learning academic skills related to reading, such as word reading accuracy, re...\n --EXCLUDES--> [?] Disorders of intellectual development\n Def: Disorders of intellectual development are a group of etiologically diverse conditions originating during the developmental period characterised by significantly below average intellectual functioning ...\n --CHILD--> [?] Disorder of intellectual development, mild\n Def: A mild disorder of intellectual development is a condition originating during the developmental period characterised by significantly below average intellectual functioning and adaptive behaviour that...", "[MC80.1] Nonspecific low blood-pressure reading\n --EXCLUDES--> [?] Maternal hypotension syndrome\n Def: Any reason for encounter to assess a mother for low blood pressure during pregnancy....\n --PARENT--> [?] Maternal care for other conditions predominantly related to pregnancy\n Def: Any reason for encounter to assess (or care for) a mother for other conditions predominantly related to pregnancy....", "[MC80.1] Nonspecific low blood-pressure reading\n --EXCLUDES--> [?] Maternal hypotension syndrome\n Def: Any reason for encounter to assess a mother for low blood pressure during pregnancy....\n --PARENT--> [?] Maternal care for other conditions predominantly related to pregnancy\n Def: Any reason for encounter to assess (or care for) a mother for other conditions predominantly related to pregnancy...." ]
MB4B.0
Dyslexia and alexia
[ { "from_icd11": "MB4B.0", "icd10_code": "R480", "icd10_title": "Dyslexia and alexia" }, { "from_icd11": "6A03.0", "icd10_code": "F810", "icd10_title": "Specific reading disorder" }, { "from_icd11": "MC80.1", "icd10_code": "R031", "icd10_title": "Nonspecific low blood-pressure reading" }, { "from_icd11": "9D93", "icd10_code": "H538", "icd10_title": "Other visual disturbances" }, { "from_icd11": "QB61.4", "icd10_code": "Z933", "icd10_title": "Colostomy status" }, { "from_icd11": "QB61.0", "icd10_code": "Z930", "icd10_title": "Tracheostomy status" }, { "from_icd11": "QB61.30", "icd10_code": "Z932", "icd10_title": "Ileostomy status" }, { "from_icd11": "QB61.5", "icd10_code": "Z9350", "icd10_title": "Unspecified cystostomy status" }, { "from_icd11": "QB61.5", "icd10_code": "Z9352", "icd10_title": "Appendico-vesicostomy status" }, { "from_icd11": "QB61.5", "icd10_code": "Z9359", "icd10_title": "Other cystostomy status" }, { "from_icd11": "QB61.5", "icd10_code": "Z9351", "icd10_title": "Cutaneous-vesicostomy status" }, { "from_icd11": "QB61.5", "icd10_code": "Z935", "icd10_title": "Cystostomy status" } ]
R480
Dyslexia and alexia
No gross improvement was seen after the methylprednisolone treatment, however, the patient refused gait assessment and was selectively mute, continuing to lie in bed with her head covered, refusing all medical care. Catatonia was suspected and 2 mg lorazepam trial was initiated 3 days later with the first dose administered intramuscularly along with haloperidol 5 mg and diphenhydramine 50 mg due to the patient's severe agitation. Ten-minutes after the first dose of lorazepam, the patient sat up at the bedside and was seen calling her family members, she participated with vital signs and maintenance medical management for the first time in over a week. A 1-h electroencephalogram was now allowed by the patient which showed no seizure activity and background slowing of 6–7 Hz. The patient's behavior continued to improve. Extensive psychiatric evaluation and the patient's family confirming no prior psychiatric history or episodes ruled out psychiatric origin of the patient's catatonia. The patient's ability to walk was significantly improved but still requiring a front-wheel walker. Prior to discharge, a third LP found normal CSF. CSF analysis was sent to Quest diagnostics NMDA-receptor antibodies and anti-Hu antibodies which returned negative. CSF COVID-19 PCR returned negative. Outpatient follow-up 1 week later showed further continued improvement no longer requiring the use of a front-wheel walker.
3.710938
0.98291
sec[1]/p[3]
en
0.999996
34381391
https://doi.org/10.3389/fpsyt.2021.696347
[ "psychiatric", "improvement", "catatonia", "lorazepam", "family", "which", "requiring", "front", "wheel", "walker" ]
[ { "code": "6E8Z", "title": "Mental, behavioural or neurodevelopmental disorders, unspecified" }, { "code": "QA00.3", "title": "General mental examination" }, { "code": "QC65", "title": "Family history of mental or behavioural disorder" }, { "code": "QA04.6", "title": "General mental examination, requested by authority" }, { "code": "FB83.1Y", "title": "Other specified osteoporosis" }, { "code": "6A4Z", "title": "Catatonia, unspecified" }, { "code": "NE60", "title": "Harmful effects of drugs, medicaments or biological substances, not elsewhere classified" }, { "code": "6A41", "title": "Catatonia induced by substances or medications" }, { "code": "6E69", "title": "Secondary catatonia syndrome" }, { "code": "6A40", "title": "Catatonia associated with another mental disorder" } ]
=== ICD-11 CODES FOUND === [6E8Z] Mental, behavioural or neurodevelopmental disorders, unspecified Also known as: Mental, behavioural or neurodevelopmental disorders, unspecified | Psychiatric disorder | mental disease NOS | mental disorder NOS | mental illness [QA00.3] General mental examination Also known as: General mental examination | mental health evaluation | general psychiatric examination Excludes: examination requested for medicolegal reasons [QC65] Family history of mental or behavioural disorder Also known as: Family history of mental or behavioural disorder | family history of psychiatric disorder | Family history of intellectual development disorder | Family history of mental retardation | Family history of conditions classifiable as intellectual development disorder [QA04.6] General mental examination, requested by authority Also known as: General mental examination, requested by authority | evaluation of mental health requested by authority | psychiatric examination requested by authority | general psychiatric examination, requested by authority [FB83.1Y] Other specified osteoporosis Also known as: Other specified osteoporosis | Osteoporosis due to eating disorders | Osteoporosis due to anorexia | Osteoporosis due to bulimia | Osteoporosis due to pregnancy or lactation [6A4Z] Catatonia, unspecified Also known as: Catatonia, unspecified | catatonia NOS | catatonic 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 [6A41] Catatonia induced by substances or medications Definition: Catatonia induced by substances or medications is a syndrome of primarily psychomotor disturbances, characterized by the co-occurrence of several symptoms of decreased, increased, or abnormal psychomotor activity, which develops during or soon after intoxication or withdrawal from certain psychoactive substances, including phencyclidine (PCP), cannabis, hallucinogens such as mescaline or LSD, cocaine and MDMA or related drugs, or during the use of certain psychoactive and non-psychoactive medica Also known as: Catatonia induced by substances or medications | Catatonia induced by psychoactive substances, including medications | Catatonia induced by specified psychoactive substance or medication | Catatonia induced by unknown or unspecified psychoactive substance Excludes: Neuroleptic malignant syndrome | Serotonin syndrome [6E69] Secondary catatonia syndrome Definition: Secondary catatonia syndrome is a syndrome of primarily psychomotor disturbances, characterized by the co-occurrence of several symptoms of decreased, increased, or abnormal psychomotor activity, which occurs as a direct pathophysiological consequence of a medical condition not classified under Mental, Behavioural or Neurodevelopmental Disorders. Examples of medical conditions that may be associated with Catatonia include diabetic ketoacidosis, hypercalcaemia, hepatic encephalopathy, homocystinu Also known as: Secondary catatonia syndrome [6A40] Catatonia associated with another mental disorder Definition: Catatonia associated with another mental disorder is a syndrome of primarily psychomotor disturbances, characterized by the co-occurrence of several symptoms of decreased, increased, or abnormal psychomotor activity, which occurs in the context of another mental disorder, such as Schizophrenia or Other Primary Psychotic Disorders, Mood Disorders, and Neurodevelopmental Disorders, especially Autism Spectrum Disorder. Also known as: Catatonia associated with another mental disorder === GRAPH WALKS === --- Walk 1 --- [6E8Z] Mental, behavioural or neurodevelopmental disorders, unspecified --PARENT--> [06] Mental, behavioural or neurodevelopmental disorders Def: Mental, behavioural and neurodevelopmental disorders are syndromes characterised by clinically significant disturbance in an individual's cognition, emotional regulation, or behaviour that reflects a ... --RELATED_TO--> [?] Sexual dysfunctions Def: Sexual Dysfunctions are syndromes that comprise the various ways in which adult people may have difficulty experiencing personally satisfying, non-coercive sexual activities. Sexual response is a comp... --- Walk 2 --- [6E8Z] Mental, behavioural or neurodevelopmental disorders, unspecified --PARENT--> [06] Mental, behavioural or neurodevelopmental disorders Def: Mental, behavioural and neurodevelopmental disorders are syndromes characterised by clinically significant disturbance in an individual's cognition, emotional regulation, or behaviour that reflects a ... --PARENT--> [?] ICD-11 for Mortality and Morbidity Statistics --- Walk 3 --- [QA00.3] General mental examination --EXCLUDES--> [?] Examination or observation for reasons other than suspected diseases or conditions or administrative purposes --CHILD--> [?] Blood-alcohol or blood-drug test --- Walk 4 --- [QA00.3] General mental examination --EXCLUDES--> [?] Examination or observation for reasons other than suspected diseases or conditions or administrative purposes --CHILD--> [?] Alcohol and drug testing other than by blood --- Walk 5 --- [QC65] Family history of mental or behavioural disorder --PARENT--> [?] Family history of health problems --CHILD--> [QC62] Family history of diseases of the blood or blood-forming organs --- Walk 6 --- [QC65] Family history of mental or behavioural disorder --PARENT--> [?] Family history of health problems --CHILD--> [QC61] Family history of malignant neoplasm
[ "[6E8Z] Mental, behavioural or neurodevelopmental disorders, unspecified\n --PARENT--> [06] Mental, behavioural or neurodevelopmental disorders\n Def: Mental, behavioural and neurodevelopmental disorders are syndromes characterised by clinically significant disturbance in an individual's cognition, emotional regulation, or behaviour that reflects a ...\n --RELATED_TO--> [?] Sexual dysfunctions\n Def: Sexual Dysfunctions are syndromes that comprise the various ways in which adult people may have difficulty experiencing personally satisfying, non-coercive sexual activities. Sexual response is a comp...", "[6E8Z] Mental, behavioural or neurodevelopmental disorders, unspecified\n --PARENT--> [06] Mental, behavioural or neurodevelopmental disorders\n Def: Mental, behavioural and neurodevelopmental disorders are syndromes characterised by clinically significant disturbance in an individual's cognition, emotional regulation, or behaviour that reflects a ...\n --PARENT--> [?] ICD-11 for Mortality and Morbidity Statistics", "[QA00.3] General mental examination\n --EXCLUDES--> [?] Examination or observation for reasons other than suspected diseases or conditions or administrative purposes\n --CHILD--> [?] Blood-alcohol or blood-drug test", "[QA00.3] General mental examination\n --EXCLUDES--> [?] Examination or observation for reasons other than suspected diseases or conditions or administrative purposes\n --CHILD--> [?] Alcohol and drug testing other than by blood", "[QC65] Family history of mental or behavioural disorder\n --PARENT--> [?] Family history of health problems\n --CHILD--> [QC62] Family history of diseases of the blood or blood-forming organs", "[QC65] Family history of mental or behavioural disorder\n --PARENT--> [?] Family history of health problems\n --CHILD--> [QC61] Family history of malignant neoplasm" ]
6E8Z
Mental, behavioural or neurodevelopmental disorders, unspecified
[ { "from_icd11": "6E8Z", "icd10_code": "F99", "icd10_title": "Mental disorder, not otherwise specified" }, { "from_icd11": "6E8Z", "icd10_code": "F488", "icd10_title": "Other specified nonpsychotic mental disorders" }, { "from_icd11": "6E8Z", "icd10_code": "F988", "icd10_title": "Other specified behavioral and emotional disorders with onset usually occurring in childhood and adolescence" }, { "from_icd11": "6E8Z", "icd10_code": "F530", "icd10_title": "Postpartum depression" }, { "from_icd11": "6E8Z", "icd10_code": "F688", "icd10_title": "Other specified disorders of adult personality and behavior" }, { "from_icd11": "6E8Z", "icd10_code": "F59", "icd10_title": "Unspecified behavioral syndromes associated with physiological disturbances and physical factors" }, { "from_icd11": "6E8Z", "icd10_code": "V", "icd10_title": "" }, { "from_icd11": "6E8Z", "icd10_code": "F531", "icd10_title": "Puerperal psychosis" }, { "from_icd11": "6E8Z", "icd10_code": "F538", "icd10_title": "" }, { "from_icd11": "6E8Z", "icd10_code": "F539", "icd10_title": "" }, { "from_icd11": "6E8Z", "icd10_code": "F680", "icd10_title": "" }, { "from_icd11": "6E8Z", "icd10_code": "F989", "icd10_title": "Unspecified behavioral and emotional disorders with onset usually occurring in childhood and adolescence" }, { "from_icd11": "6E8Z", "icd10_code": "F99-F99", "icd10_title": "" }, { "from_icd11": "6E8Z", "icd10_code": "F00-F09", "icd10_title": "" }, { "from_icd11": "6E8Z", "icd10_code": "F40-F48", "icd10_title": "" } ]
F99
Mental disorder, not otherwise specified
Crnej et al. reported a 71-year-old male with a history of endothelial decompensation after phacoemulsification and who underwent DMEK of the right eye for five months . He developed a decrease in vision seven days after the first dose of the BNT162b2 COVID-19 vaccine. A right eye conjunctival injection and corneal edema were noted. The central corneal thickness was 714 μm, and corneal endothelial graft rejection was diagnosed. Phylactou et al. reported two cases with a history of Fuchs endothelial corneal dystrophy who underwent DMEK with acute corneal endothelial graft rejection after administration of BNT162b2 COVID-19 vaccine . A 66-year-old female who underwent DMEK of the right eye 21 days prior developed blurred vision seven days after the first dose of the vaccine. Right eye conjunctival injection, diffuse corneal edema, and fine KPs were noted, and corneal endothelial graft rejection of the right eye was diagnosed. Another 83-year-old female underwent DMEK six and three years prior in the right and left eyes, respectively. She had bilateral blurring of vision, pain, photophobia, and redness three weeks after the second dose of the vaccine. Bilateral circumcorneal injections, KPs, and AC inflammation were also noted. The central corneal thickness was 660 µm and 622 µm in the right and left eyes, respectively. A diagnosis of bilateral simultaneous acute endothelial graft rejection was made.
3.988281
0.895996
sec[2]/sec[1]/p[2]
en
0.999996
34960150
https://doi.org/10.3390/vaccines9121404
[ "corneal", "endothelial", "dmek", "vaccine", "graft", "rejection", "vision", "seven", "covid", "conjunctival" ]
[ { "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": "1F00.10", "title": "Herpes simplex keratitis" }, { "code": "9A70.0", "title": "Endothelial corneal dystrophy" }, { "code": "LA11.5", "title": "Congenital corneal opacity" }, { "code": "2F2Y", "title": "Other specified benign cutaneous neoplasms" }, { "code": "LA11.Y", "title": "Other specified structural developmental anomalies of the anterior segment of eye" } ]
=== 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 [1F00.10] Herpes simplex keratitis Definition: 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 disorders based on the site of infection. This diagnosis is a condition in which the eye's cornea, the front part of the eye, becomes infected and inflamed. Also known as: Herpes simplex keratitis | herpetic keratitis | herpesviral keratitis | disciform keratitis | herpes keratitis [9A70.0] Endothelial corneal dystrophy Also known as: Endothelial corneal dystrophy | dystrophy of corneal endothelium | Posterior corneal dystrophy | Congenital hereditary endothelial dystrophy type 2 | Fuchs endothelial corneal dystrophy [LA11.5] Congenital corneal opacity Definition: A condition caused by failure of the cornea to correctly develop during the antenatal period. This condition is characterised by opacity of the cornea. Also known as: Congenital corneal opacity | Congenital corneal opacity, unilateral | Congenital corneal opacity, bilateral | Posterior polymorphous corneal dystrophy | PPCD - [Posterior polymorphous corneal dystrophy] C1 or C2 [2F2Y] Other specified benign cutaneous neoplasms Also known as: Other specified benign cutaneous neoplasms | Benign tumours of cutaneous smooth muscle | Pilar leiomyoma | Cutaneous leiomyoma | Piloleiomyoma [LA11.Y] Other specified structural developmental anomalies of the anterior segment of eye Also known as: Other specified structural developmental anomalies of the anterior segment of eye | Structural developmental anomalies of the pupil | Corectopia | Polycoria | multiple pupil === 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--> [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 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... --PARENT--> [?] Disorders of the eyeball - anterior segment Def: This refers to any disorders of the front third of the eye that includes the structures in front of the vitreous humour: the cornea, iris, ciliary body, and lens.... --- Walk 3 --- [9A71] Infectious keratitis --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 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... --PARENT--> [?] Disorders of the eyeball - anterior segment Def: This refers to any disorders of the front third of the eye that includes the structures in front of the vitreous humour: the cornea, iris, ciliary body, and lens.... --- 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--> [9A70] Hereditary corneal dystrophies\n Def: The term corneal dystrophy embraces a heterogeneous group of bilateral genetically determined non-inflammatory corneal diseases that are usually restricted to the cornea. The designation is imprecise ...", "[9A7Z] Disorders of the cornea, unspecified\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 --PARENT--> [?] Disorders of the eyeball - anterior segment\n Def: This refers to any disorders of the front third of the eye that includes the structures in front of the vitreous humour: the cornea, iris, ciliary body, and lens....", "[9A71] Infectious keratitis\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", "[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 --PARENT--> [?] Disorders of the eyeball - anterior segment\n Def: This refers to any disorders of the front third of the eye that includes the structures in front of the vitreous humour: the cornea, iris, ciliary body, and lens....", "[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
For the patient described, a differential diagnosis was created. Various medical disorders can cause hallucinations and should be the first to be excluded. These include, but are not limited to, electrolyte imbalance, nutritional deficits, thyroid disease, Wilson’s disease, porphyria, adrenal disease, migraines, seizures, and infections such as meningitis and encephalitis . Despite the patient testing positive for parainfluenza virus type three, post-infectious encephalitis was ruled out as the patient was afebrile, experienced no symptoms of infection other than abdominal pain on the day before the hallucinations began, lacked neurological symptoms which would be expected in encephalitis (e.g., headache, neck stiffness, change in alertness or cognition), and his brain MRI was normal. Occipital lobe epilepsy was supported by the occurrence of visual hallucinations and a family history of seizures in his sister. However, hallucinations are rarely caused by epilepsy and are typically brief, lasting just a few seconds . In this patient, the initial hallucinatory episode lasted for several hours and intermittently recurred over the next few days. In addition, a 24-hour ambulatory EEG performed after hospital discharge did not detect any epileptiform activity. All other medical causes for the hallucinations were excluded due to negative exam and/or test results. Psychiatric causes were then considered.
4.054688
0.959473
sec[2]/p[0]
en
0.999998
34987903
https://doi.org/10.7759/cureus.20012
[ "hallucinations", "encephalitis", "excluded", "seizures", "epilepsy", "causes", "differential", "created", "various", "disorders" ]
[ { "code": "MB27.2Z", "title": "Hallucinations, unspecified" }, { "code": "MB27.2Y", "title": "Other specified hallucinations" }, { "code": "6E61.0", "title": "Secondary psychotic syndrome, with hallucinations" }, { "code": "MB27.27", "title": "Visual hallucinations" }, { "code": "MB27.20", "title": "Auditory hallucinations" }, { "code": "1D00.Z", "title": "Infectious encephalitis, unspecified" }, { "code": "1C80", "title": "Viral encephalitis, not elsewhere classified" }, { "code": "NE61", "title": "Harmful effects of or exposure to noxious substances, chiefly nonmedicinal as to source, not elsewhere classified" }, { "code": "1D00.0", "title": "Bacterial encephalitis" }, { "code": "8E48", "title": "Encephalitis, not elsewhere classified" } ]
=== ICD-11 CODES FOUND === [MB27.2Z] Hallucinations, unspecified Also known as: Hallucinations, unspecified | Hallucinations [MB27.2Y] Other specified hallucinations Also known as: Other specified hallucinations | Hallucinosis | Cacosmia [6E61.0] Secondary psychotic syndrome, with hallucinations Definition: A syndrome characterised by the presence of prominent hallucinations that is judged to be a direct pathophysiological consequence of a health condition not classified under mental and behavioural disorders, based on evidence from the history, physical examination, or laboratory findings. Delusions are not a prominent aspect of the clinical presentation. The symptoms are not accounted for by delirium or by another mental and behavioural disorder, and are not a psychologically mediated response to Also known as: Secondary psychotic syndrome, with hallucinations | psychotic disorder with hallucinations in conditions classified elsewhere | transient organic psychotic condition, hallucinatory type | Organic hallucinatory state | organic hallucination Excludes: Delirium | Mood disorders [MB27.27] Visual hallucinations Definition: Hallucinations involving sight in the absence of an actual visual stimulus that are not restricted to the period of awakening or the onset of sleep. Visual hallucinations may involve formed images, such as of people, or of unformed images, such as flashes of light. Visual hallucinations must be distinguished from illusions, which are visual misperceptions of real external stimuli. Also known as: Visual hallucinations | seeing things [MB27.20] Auditory hallucinations Definition: Hallucinations involving the perception of sound, most frequently of voices but sometimes of clicks or other noises, that are not restricted to the period of awakening or the onset of sleep. Also known as: Auditory hallucinations [1D00.Z] Infectious encephalitis, unspecified Also known as: Infectious encephalitis, unspecified | Infectious encephalitis, not elsewhere classified | encephalitis NOS | acute encephalitis NOS | acute brain inflammation [1C80] Viral encephalitis, not elsewhere classified Also known as: Viral encephalitis, not elsewhere classified | postviral encephalitis NOS | equine encephalitis | mosquito-borne encephalitis | acute haemorrhagic encephalitis Includes: Viral meningoencephalitis, not elsewhere classified [NE61] Harmful effects of or exposure to noxious substances, chiefly nonmedicinal as to source, not elsewhere classified Also known as: Harmful effects of or exposure to noxious substances, chiefly nonmedicinal as to source, not elsewhere classified | Harmful effects of or exposure to noxious substances chiefly nonmedicinal as to source, alcohols | alcohol poisoning | alcohol toxicity | Harmful effects of or exposure to noxious substances chiefly nonmedicinal as to source, Ethanol Excludes: corrosions | Bacterial foodborne intoxications [1D00.0] Bacterial encephalitis Also known as: Bacterial encephalitis | bacterial encephalomyelitis | Encephalitis due to Treponema pallidum [8E48] Encephalitis, not elsewhere classified Also known as: Encephalitis, not elsewhere classified | encephalitis NEC | idiopathic encephalitis === GRAPH WALKS === --- Walk 1 --- [MB27.2Z] Hallucinations, unspecified --PARENT--> [MB27.2] Hallucinations Def: Sensory perceptions of any modality occurring in the absence of the appropriate (external) stimulus. The person may or may not have insight into the unreal nature of the perception.... --CHILD--> [MB27.21] Gustatory hallucinations Def: Hallucinations of taste in the absence of an actual external stimulus.... --- Walk 2 --- [MB27.2Z] Hallucinations, unspecified --PARENT--> [MB27.2] Hallucinations Def: Sensory perceptions of any modality occurring in the absence of the appropriate (external) stimulus. The person may or may not have insight into the unreal nature of the perception.... --PARENT--> [MB27] Symptoms or signs involving perceptual disturbance Def: Symptoms and signs involving a disruption in sensory perception, including depersonalization, derealization, and hallucinations in any modality.... --- Walk 3 --- [MB27.2Y] Other specified hallucinations --PARENT--> [MB27.2] Hallucinations Def: Sensory perceptions of any modality occurring in the absence of the appropriate (external) stimulus. The person may or may not have insight into the unreal nature of the perception.... --CHILD--> [MB27.21] Gustatory hallucinations Def: Hallucinations of taste in the absence of an actual external stimulus.... --- Walk 4 --- [MB27.2Y] Other specified hallucinations --PARENT--> [MB27.2] Hallucinations Def: Sensory perceptions of any modality occurring in the absence of the appropriate (external) stimulus. The person may or may not have insight into the unreal nature of the perception.... --CHILD--> [MB27.21] Gustatory hallucinations Def: Hallucinations of taste in the absence of an actual external stimulus.... --- Walk 5 --- [6E61.0] Secondary psychotic syndrome, with hallucinations Def: A syndrome characterised by the presence of prominent hallucinations that is judged to be a direct pathophysiological consequence of a health condition not classified under mental and behavioural diso... --PARENT--> [6E61] Secondary psychotic syndrome Def: A syndrome characterised by the presence of prominent hallucinations or delusions judged to be a direct pathophysiological consequence of a health condition not classified under mental and behavioural... --EXCLUDES--> [?] Acute and transient psychotic disorder Def: Acute and transient psychotic disorder is characterised by acute onset of psychotic symptoms that emerge without a prodrome and reach their maximal severity within two weeks. Symptoms may include delu... --- Walk 6 --- [6E61.0] Secondary psychotic syndrome, with hallucinations Def: A syndrome characterised by the presence of prominent hallucinations that is judged to be a direct pathophysiological consequence of a health condition not classified under mental and behavioural diso... --EXCLUDES--> [?] Delirium Def: Delirium is characterized by a disturbance of attention, orientation, and awareness that develops within a short period of time, typically presenting as significant confusion or global neurocognitive ... --CHILD--> [?] Delirium due to multiple etiological factors Def: All definitional requirements for delirium are met. There is evidence from history, physical examination, or laboratory findings that the delirium is attributable to multiple etiological factors, whic...
[ "[MB27.2Z] Hallucinations, unspecified\n --PARENT--> [MB27.2] Hallucinations\n Def: Sensory perceptions of any modality occurring in the absence of the appropriate (external) stimulus. The person may or may not have insight into the unreal nature of the perception....\n --CHILD--> [MB27.21] Gustatory hallucinations\n Def: Hallucinations of taste in the absence of an actual external stimulus....", "[MB27.2Z] Hallucinations, unspecified\n --PARENT--> [MB27.2] Hallucinations\n Def: Sensory perceptions of any modality occurring in the absence of the appropriate (external) stimulus. The person may or may not have insight into the unreal nature of the perception....\n --PARENT--> [MB27] Symptoms or signs involving perceptual disturbance\n Def: Symptoms and signs involving a disruption in sensory perception, including depersonalization, derealization, and hallucinations in any modality....", "[MB27.2Y] Other specified hallucinations\n --PARENT--> [MB27.2] Hallucinations\n Def: Sensory perceptions of any modality occurring in the absence of the appropriate (external) stimulus. The person may or may not have insight into the unreal nature of the perception....\n --CHILD--> [MB27.21] Gustatory hallucinations\n Def: Hallucinations of taste in the absence of an actual external stimulus....", "[MB27.2Y] Other specified hallucinations\n --PARENT--> [MB27.2] Hallucinations\n Def: Sensory perceptions of any modality occurring in the absence of the appropriate (external) stimulus. The person may or may not have insight into the unreal nature of the perception....\n --CHILD--> [MB27.21] Gustatory hallucinations\n Def: Hallucinations of taste in the absence of an actual external stimulus....", "[6E61.0] Secondary psychotic syndrome, with hallucinations\n Def: A syndrome characterised by the presence of prominent hallucinations that is judged to be a direct pathophysiological consequence of a health condition not classified under mental and behavioural diso...\n --PARENT--> [6E61] Secondary psychotic syndrome\n Def: A syndrome characterised by the presence of prominent hallucinations or delusions judged to be a direct pathophysiological consequence of a health condition not classified under mental and behavioural...\n --EXCLUDES--> [?] Acute and transient psychotic disorder\n Def: Acute and transient psychotic disorder is characterised by acute onset of psychotic symptoms that emerge without a prodrome and reach their maximal severity within two weeks. Symptoms may include delu...", "[6E61.0] Secondary psychotic syndrome, with hallucinations\n Def: A syndrome characterised by the presence of prominent hallucinations that is judged to be a direct pathophysiological consequence of a health condition not classified under mental and behavioural diso...\n --EXCLUDES--> [?] Delirium\n Def: Delirium is characterized by a disturbance of attention, orientation, and awareness that develops within a short period of time, typically presenting as significant confusion or global neurocognitive ...\n --CHILD--> [?] Delirium due to multiple etiological factors\n Def: All definitional requirements for delirium are met. There is evidence from history, physical examination, or laboratory findings that the delirium is attributable to multiple etiological factors, whic..." ]
MB27.2Z
Hallucinations, unspecified
[ { "from_icd11": "MB27.2Z", "icd10_code": "R443", "icd10_title": "Hallucinations, unspecified" }, { "from_icd11": "MB27.2Z", "icd10_code": "R442", "icd10_title": "Other hallucinations" }, { "from_icd11": "6E61.0", "icd10_code": "F060", "icd10_title": "Psychotic disorder with hallucinations due to known physiological condition" }, { "from_icd11": "MB27.27", "icd10_code": "R441", "icd10_title": "Visual hallucinations" }, { "from_icd11": "MB27.20", "icd10_code": "R440", "icd10_title": "Auditory hallucinations" }, { "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": "1C80", "icd10_code": "A86", "icd10_title": "Unspecified viral encephalitis" } ]
R443
Hallucinations, unspecified
A 40-year-old right-handed male patient with a past medical history of migraine presented in the emergency department of a tertiary care hospital with complaints of headache, blurry vision, a progressive right-sided weakness for the past seven hours. He was diagnosed with migraine with aura for two years and had similar flares in the past but did not seek medical help as symptoms always resolved within a few hours with no residual deficits. His blood pressure at the time of presentation was 175/95 mmHg in the right arm; oral temperature 100 F; pulse 89 bpm. Headache was sudden without aura, 8/10 in intensity, unilateral on the right side, pulsatile, associated with vomiting, aggravated by speaking and light, and relieved by dimming the lights. Physical examination showed decreased power (0/5) and increased tone on the right side of the arm. The rest of the motor examination showed normal bulk, tone, and power. Neck extension and flexion were 5/5. Cranial nerves III-XII were intact. Babinski’s sign was positive on the right side. The rest of the physical examination was unremarkable. The patient was started on dihydroergotamine (DHE) and nitroglycerin in the emergency department. Non-contrast computed tomography (CT) was negative for acute bleeding. During the emergency department stay, the patient had an episode of generalized seizure, which lasted for four minutes and was managed by IV lorazepam.
3.759766
0.984863
sec[1]/p[0]
en
0.999999
34239789
https://doi.org/10.7759/cureus.15355
[ "past", "emergency", "department", "side", "migraine", "headache", "hours", "aura", "physical", "power" ]
[ { "code": "PL13.8", "title": "Expired or deteriorated medication or substance, as mode of injury or harm" }, { "code": "BA50", "title": "Old myocardial infarction" }, { "code": "8B25.4", "title": "Late effects of stroke not known if ischaemic or haemorrhagic" }, { "code": "QE51.1", "title": "History of spouse or partner violence" }, { "code": "PB36", "title": "Unintentional exposure to or harmful effects of other or unspecified substances chiefly nonmedicinal as to source" }, { "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 === [PL13.8] Expired or deteriorated medication or substance, as mode of injury or harm Also known as: Expired or deteriorated medication or substance, as mode of injury or harm | drug past expiry date | expired drug | deteriorated drug | drug past due date [BA50] Old myocardial infarction Definition: Past myocardial infarction diagnosed by electrocardiogram (ECG) or other special investigation, but currently presenting no symptoms. Also known as: Old myocardial infarction | past myocardial infarction | healed myocardial infarction | myocardial scar | myocardial scarring Includes: healed myocardial infarction [8B25.4] Late effects of stroke not known if ischaemic or haemorrhagic Definition: Late effects occurring 1 month or later after the onset of the disease. Codes for acute stroke should be exclusively used for the acute stroke and immediately related hospitalisation episodes. Also known as: Late effects of stroke not known if ischaemic or haemorrhagic | sequelae of stroke, not specified as haemorrhage or infarction | old cerebrovascular accident | old CVA - [cerebrovascular accident] | old stroke [QE51.1] History of spouse or partner violence Definition: Non-accidental acts of physical force, forced or coerced sexual acts, verbal or symbolic acts, or significant caregiving omissions that result in harm to a spouse or intimate partner or that have a reasonable potential for harm. Also known as: History of spouse or partner violence | spouse violence | partner violence | History of spouse or partner violence, physical | partner physical violence [PB36] Unintentional exposure to or harmful effects of other or unspecified substances chiefly nonmedicinal as to source Also known as: Unintentional exposure to or harmful effects of other or unspecified substances chiefly nonmedicinal as to source | Unintentional exposure to or harmful effects of other or unspecified gases, fumes or vapours | Unintentional exposure to or harmful effects of nitrogen oxides | Unintentional exposure to or harmful effects of sulfur dioxide | Unintentional exposure to or harmful effects of formaldehyde [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 --- [PL13.8] Expired or deteriorated medication or substance, 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 2 --- [PL13.8] Expired or deteriorated medication or substance, as mode of injury or harm --PARENT--> [PL13] Mode of injury or harm associated with exposure to a drug, medicament or biological substance --PARENT--> [?] Causes of healthcare related harm or injury --- Walk 3 --- [BA50] Old myocardial infarction Def: Past myocardial infarction diagnosed by electrocardiogram (ECG) or other special investigation, but currently presenting no symptoms.... --PARENT--> [?] Chronic ischaemic heart disease Def: Chronic heart disease is seen due to the atherosclerosis of coronary arteries. It is characterised by angina pectoris and unstable angina.... --CHILD--> [BA51] Ischaemic cardiomyopathy Def: Ischaemic cardiomyopathy has been defined as left ventricular systolic dysfunction with one or more of the following: a history of prior myocardial revascularisation or myocardial infarction, more tha... --- Walk 4 --- [BA50] Old myocardial infarction Def: Past myocardial infarction diagnosed by electrocardiogram (ECG) or other special investigation, but currently presenting no symptoms.... --PARENT--> [?] Chronic ischaemic heart disease Def: Chronic heart disease is seen due to the atherosclerosis of coronary arteries. It is characterised by angina pectoris and unstable angina.... --CHILD--> [BA51] Ischaemic cardiomyopathy Def: Ischaemic cardiomyopathy has been defined as left ventricular systolic dysfunction with one or more of the following: a history of prior myocardial revascularisation or myocardial infarction, more tha... --- Walk 5 --- [8B25.4] 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--> [8B25] 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... --CHILD--> [8B25.1] Late effects of intracerebral haemorrhage --- Walk 6 --- [8B25.4] 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--> [8B25] 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... --CHILD--> [8B25.2] Late effects of subarachnoid haemorrhage Def: Late effects of non-traumatic subarachnoid haemorrhage 1 month or later after the onset of the disease. Codes for acute haemorrhage should be exclusively used for the acute haemorrhage and immediately...
[ "[PL13.8] Expired or deteriorated medication or substance, 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", "[PL13.8] Expired or deteriorated medication or substance, 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 --PARENT--> [?] Causes of healthcare related harm or injury", "[BA50] Old myocardial infarction\n Def: Past myocardial infarction diagnosed by electrocardiogram (ECG) or other special investigation, but currently presenting no symptoms....\n --PARENT--> [?] Chronic ischaemic heart disease\n Def: Chronic heart disease is seen due to the atherosclerosis of coronary arteries. It is characterised by angina pectoris and unstable angina....\n --CHILD--> [BA51] Ischaemic cardiomyopathy\n Def: Ischaemic cardiomyopathy has been defined as left ventricular systolic dysfunction with one or more of the following: a history of prior myocardial revascularisation or myocardial infarction, more tha...", "[BA50] Old myocardial infarction\n Def: Past myocardial infarction diagnosed by electrocardiogram (ECG) or other special investigation, but currently presenting no symptoms....\n --PARENT--> [?] Chronic ischaemic heart disease\n Def: Chronic heart disease is seen due to the atherosclerosis of coronary arteries. It is characterised by angina pectoris and unstable angina....\n --CHILD--> [BA51] Ischaemic cardiomyopathy\n Def: Ischaemic cardiomyopathy has been defined as left ventricular systolic dysfunction with one or more of the following: a history of prior myocardial revascularisation or myocardial infarction, more tha...", "[8B25.4] 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--> [8B25] 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...\n --CHILD--> [8B25.1] Late effects of intracerebral haemorrhage", "[8B25.4] 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--> [8B25] 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...\n --CHILD--> [8B25.2] Late effects of subarachnoid haemorrhage\n Def: Late effects of non-traumatic subarachnoid haemorrhage 1 month or later after the onset of the disease. Codes for acute haemorrhage should be exclusively used for the acute haemorrhage and immediately..." ]
PL13.8
Expired or deteriorated medication or substance, as mode of injury or harm
[ { "from_icd11": "BA50", "icd10_code": "I252", "icd10_title": "Old myocardial infarction" }, { "from_icd11": "8B25.4", "icd10_code": "I694", "icd10_title": "" }, { "from_icd11": "PB36", "icd10_code": "X49", "icd10_title": "" }, { "from_icd11": "JB22.1", "icd10_code": "O821", "icd10_title": "" } ]
I252
Old myocardial infarction
The Marshall vein (VOM), due to its embryological specificity and unique anatomical-functional characteristics, has been recognized for its significant involvement in the initiation and perpetuation of atrial fibrillation (AF) and other atrial arrhythmias . While endocardial radiofrequency ablation stands as a crucial therapeutic intervention for AF, its efficacy in eliminating the arrhythmogenic potential mediated by the VOM in certain patients has shown limitations. This limitation provides an anatomical and physiological rationale for the recurrence of AF and the persistence of atrial arrhythmias. Chemical ablation, specifically the administration of anhydrous ethanol into the VOM, emerges as a more definitive technique targeting the atrial musculature associated with the VOM, which can effectively isolate pulmonary vein potentials. This approach creates favorable conditions for subsequent catheter radiofrequency ablation, mitigating postoperative leak points and enhancing the isolation rate of pulmonary vein potentials during AF radiofrequency ablation, thus reducing the incidence of postoperative atrial tachycardia and AF recurrence associated with the VOM. We report a case in which a patient developed hypoxia and hypotension following VOM ethanol infusion for persistent AF, which required dopamine and supplemental oxygen for stabilization before gradual recovery over the subsequent ten days.
4.273438
0.841797
sec[0]/p[0]
en
0.999997
39886114
https://doi.org/10.11604/pamj.2024.49.37.44226
[ "atrial", "ablation", "vein", "radiofrequency", "which", "anatomical", "arrhythmias", "this", "recurrence", "ethanol" ]
[ { "code": "BC46&XA91S4", "title": "Atrial thrombosis" }, { "code": "LA8Z", "title": "Structural developmental anomaly of heart or great vessels, unspecified" }, { "code": "BC40.Z", "title": "Acquired atrial abnormality, unspecified" }, { "code": "BC81.2Z", "title": "Macro reentrant atrial tachycardia, unspecified" }, { "code": "LA8Y", "title": "Other specified structural developmental anomaly of heart or great vessels" }, { "code": "QF01.10", "title": "Acquired absence of female genital organs" }, { "code": "9B73.3", "title": "Serous retinal detachment" }, { "code": "JA8C.Z", "title": "Maternal care related to premature separation of placenta, unspecified" }, { "code": "KA02.Y", "title": "Fetus or newborn affected by other specified complication of placenta" }, { "code": "5D40.00", "title": "Hypothyroidism postradioactive iodine ablation" } ]
=== ICD-11 CODES FOUND === [LA8Z] Structural developmental anomaly of heart or great vessels, unspecified Also known as: Structural developmental anomaly of heart or great vessels, unspecified | Heart malformations | Cardiac malformations | congenital anomaly of heart | congenital heart disease [BC40.Z] Acquired atrial abnormality, unspecified Also known as: Acquired atrial abnormality, unspecified | Acquired atrial abnormality [BC81.2Z] Macro reentrant atrial tachycardia, unspecified Also known as: Macro reentrant atrial tachycardia, unspecified | Macro reentrant atrial tachycardia | MRAT - [macro re-entrant atrial tachycardia] | intra-atrial re-entry tachycardia | Atrial flutter NOS [LA8Y] Other specified structural developmental anomaly of heart or great vessels Also known as: Other specified structural developmental anomaly of heart or great vessels | Congenital anomaly of position or spatial relationships of thoraco-abdominal organs | Usual atrial arrangement | atrial situs solitus | Abnormal atrial arrangement [QF01.10] Acquired absence of female genital organs Also known as: Acquired absence of female genital organs | Acquired absence of cervix | amputation of cervix | Acquired absence of the uterus | acquired uterine absence [9B73.3] Serous retinal detachment Definition: This occurs due to inflammation, injury or vascular abnormalities that results in fluid accumulating underneath the retina without the presence of a hole, tear, or break. Also known as: Serous retinal detachment | serous retinal detachment, unspecified eye | sensory retinal detachment | Retinal detachment without retinal break | Retinal detachment NOS Excludes: Central serous chorioretinopathy [JA8C.Z] Maternal care related to premature separation of placenta, unspecified Also known as: Maternal care related to premature separation of placenta, unspecified | Maternal care related to premature separation of placenta | ablatio placentae | detachment of placenta | placenta abruptio [KA02.Y] Fetus or newborn affected by other specified complication of placenta Also known as: Fetus or newborn affected by other specified complication of placenta | Fetus or newborn affected by other forms of placental separation | Ablatio placentae affecting fetus or newborn | placenta ablation affecting fetus or newborn | Abruptio placentae affecting fetus or newborn [5D40.00] Hypothyroidism postradioactive iodine ablation Also known as: Hypothyroidism postradioactive iodine ablation === GRAPH WALKS === --- Walk 1 --- [LA8Z] Structural developmental anomaly of heart or great vessels, unspecified --PARENT--> [?] Structural developmental anomaly of heart or great vessels Def: A congenital malformation of the heart and/or great vessels or an acquired abnormality unique to the congenitally malformed heart.... --RELATED_TO--> [?] Congenital cardiac tumor, not otherwise specified Def: A congenital malformation consisting of growth of abnormal tissue within the heart.... --- Walk 2 --- [LA8Z] Structural developmental anomaly of heart or great vessels, unspecified --PARENT--> [?] Structural developmental anomaly of heart or great vessels Def: A congenital malformation of the heart and/or great vessels or an acquired abnormality unique to the congenitally malformed heart.... --RELATED_TO--> [?] Congenital cardiac tumor, not otherwise specified Def: A congenital malformation consisting of growth of abnormal tissue within the heart.... --- Walk 3 --- [BC40.Z] Acquired atrial abnormality, unspecified --PARENT--> [BC40] Acquired atrial abnormality Def: A postnatal pathological change in form or function of one or both atriums.... --RELATED_TO--> [?] Postprocedural left atrial complication Def: An event or occurrence affecting the morphologically left atrium that is associated with a healthcare intervention, is a departure from the desired course of events, and may cause, or be associated wi... --- Walk 4 --- [BC40.Z] Acquired atrial abnormality, unspecified --PARENT--> [BC40] Acquired atrial abnormality Def: A postnatal pathological change in form or function of one or both atriums.... --RELATED_TO--> [?] Postprocedural residual or recurrent interatrial communication Def: A persistent or recurrent hole or pathway between the atrial chambers, including intentional residual communications.... --- Walk 5 --- [BC81.2Z] Macro reentrant atrial tachycardia, unspecified --PARENT--> [BC81.2] Macro reentrant atrial tachycardia Def: An atrial arrhythmia in which there is intra-atrial reentry or circus movement around a fixed or functional central obstacle. The central obstacle may consist of normal (e.g. valves) or abnormal (e.g.... --CHILD--> [BC81.22] Scar mediated macro reentrant atrial tachycardia Def: A macro re-entrant atrial tachycardia in which the central obstacle and/or the zone of slow conduction sustaining the tachycardia is due to scar. In this context scar generally refers to surgical or i... --- Walk 6 --- [BC81.2Z] Macro reentrant atrial tachycardia, unspecified --PARENT--> [BC81.2] Macro reentrant atrial tachycardia Def: An atrial arrhythmia in which there is intra-atrial reentry or circus movement around a fixed or functional central obstacle. The central obstacle may consist of normal (e.g. valves) or abnormal (e.g.... --PARENT--> [BC81] Supraventricular tachyarrhythmia Def: Tachycardia originating at or above the atrioventricular (AV) node, usually with a narrow QRS or QRS complex similar to the sinus QRS morphology....
[ "[LA8Z] Structural developmental anomaly of heart or great vessels, unspecified\n --PARENT--> [?] Structural developmental anomaly of heart or great vessels\n Def: A congenital malformation of the heart and/or great vessels or an acquired abnormality unique to the congenitally malformed heart....\n --RELATED_TO--> [?] Congenital cardiac tumor, not otherwise specified\n Def: A congenital malformation consisting of growth of abnormal tissue within the heart....", "[LA8Z] Structural developmental anomaly of heart or great vessels, unspecified\n --PARENT--> [?] Structural developmental anomaly of heart or great vessels\n Def: A congenital malformation of the heart and/or great vessels or an acquired abnormality unique to the congenitally malformed heart....\n --RELATED_TO--> [?] Congenital cardiac tumor, not otherwise specified\n Def: A congenital malformation consisting of growth of abnormal tissue within the heart....", "[BC40.Z] Acquired atrial abnormality, unspecified\n --PARENT--> [BC40] Acquired atrial abnormality\n Def: A postnatal pathological change in form or function of one or both atriums....\n --RELATED_TO--> [?] Postprocedural left atrial complication\n Def: An event or occurrence affecting the morphologically left atrium that is associated with a healthcare intervention, is a departure from the desired course of events, and may cause, or be associated wi...", "[BC40.Z] Acquired atrial abnormality, unspecified\n --PARENT--> [BC40] Acquired atrial abnormality\n Def: A postnatal pathological change in form or function of one or both atriums....\n --RELATED_TO--> [?] Postprocedural residual or recurrent interatrial communication\n Def: A persistent or recurrent hole or pathway between the atrial chambers, including intentional residual communications....", "[BC81.2Z] Macro reentrant atrial tachycardia, unspecified\n --PARENT--> [BC81.2] Macro reentrant atrial tachycardia\n Def: An atrial arrhythmia in which there is intra-atrial reentry or circus movement around a fixed or functional central obstacle. The central obstacle may consist of normal (e.g. valves) or abnormal (e.g....\n --CHILD--> [BC81.22] Scar mediated macro reentrant atrial tachycardia\n Def: A macro re-entrant atrial tachycardia in which the central obstacle and/or the zone of slow conduction sustaining the tachycardia is due to scar. In this context scar generally refers to surgical or i...", "[BC81.2Z] Macro reentrant atrial tachycardia, unspecified\n --PARENT--> [BC81.2] Macro reentrant atrial tachycardia\n Def: An atrial arrhythmia in which there is intra-atrial reentry or circus movement around a fixed or functional central obstacle. The central obstacle may consist of normal (e.g. valves) or abnormal (e.g....\n --PARENT--> [BC81] Supraventricular tachyarrhythmia\n Def: Tachycardia originating at or above the atrioventricular (AV) node, usually with a narrow QRS or QRS complex similar to the sinus QRS morphology...." ]
BC46&XA91S4
Atrial thrombosis
[ { "from_icd11": "LA8Z", "icd10_code": "Q248", "icd10_title": "Other specified congenital malformations of heart" }, { "from_icd11": "LA8Z", "icd10_code": "Q893", "icd10_title": "Situs inversus" }, { "from_icd11": "LA8Z", "icd10_code": "Q212", "icd10_title": "Atrioventricular septal defect" }, { "from_icd11": "LA8Z", "icd10_code": "Q249", "icd10_title": "Congenital malformation of heart, unspecified" }, { "from_icd11": "LA8Z", "icd10_code": "Q246", "icd10_title": "Congenital heart block" }, { "from_icd11": "LA8Z", "icd10_code": "Q242", "icd10_title": "Cor triatriatum" }, { "from_icd11": "LA8Z", "icd10_code": "Q219", "icd10_title": "Congenital malformation of cardiac septum, unspecified" }, { "from_icd11": "LA8Z", "icd10_code": "Q208", "icd10_title": "Other congenital malformations of cardiac chambers and connections" }, { "from_icd11": "LA8Z", "icd10_code": "Q897", "icd10_title": "Multiple congenital malformations, not elsewhere classified" }, { "from_icd11": "LA8Z", "icd10_code": "Q209", "icd10_title": "Congenital malformation of cardiac chambers and connections, unspecified" }, { "from_icd11": "LA8Z", "icd10_code": "Q218", "icd10_title": "Other congenital malformations of cardiac septa" }, { "from_icd11": "LA8Z", "icd10_code": "Q20", "icd10_title": "Congenital malformations of cardiac chambers and connections" }, { "from_icd11": "LA8Z", "icd10_code": "Q206", "icd10_title": "Isomerism of atrial appendages" }, { "from_icd11": "LA8Z", "icd10_code": "Q21", "icd10_title": "Congenital malformations of cardiac septa" }, { "from_icd11": "LA8Z", "icd10_code": "Q226", "icd10_title": "Hypoplastic right heart syndrome" } ]
Q248
Other specified congenital malformations of heart
Surprisingly, there was no significant hematologic toxicity after 12 months of treatment. The MRD has always been negative. He has been going to school and lived a normal life. During this time, there were only 2 mild infective fever episodes. Now, let me report his laboratory examinations. In peripheral blood, hemoglobin was above 100 g/L and platelet count was higher than 100 × 10 9 /L when measured at all timepoints . After using trametinib, the WBC fluctuated between 2.4 and 7.14 × 10 9 /L. Moreover, WBC remained above 3 × 10 9 /L more frequently after using trametinib than before introducing the drug (83%=20/24 vs 77% = 14/18). The absolute neutrophil count (ANC) fluctuated between 0 and 4.42 × 10 9 /L, only falling below 0.5 × 10 9 /L in 4 instances. Moreover, ANC remained above 0.5 × 10 9 /L more frequently after using trametinib than before introducing the drug (83% = 20/24 vs 72% = 13/18) . Glutamic amino transferase and aspartic amino transferase serum values were 15.25 and 27.714 U/L before using trametinib, and 31.625 and 27 U/L after using trametinib, respectively. Creatinine and urea concentrations were 37.87 vs 42 μmol/L and 4.125 vs 3.9 mmol/L before and after using trametinib, respectively . During the trametinib regime, 2 echocardiographic evaluations were performed. Cardiac ejection fraction was 60% and 66%. MRD assessment was performed every 3 months, showing negative results .
4.054688
0.640625
sec[1]/p[4]
en
0.999997
34160436
https://doi.org/10.1097/MD.0000000000026440
[ "trametinib", "using", "count", "fluctuated", "moreover", "remained", "frequently", "introducing", "drug", "amino" ]
[ { "code": "QE11.Z", "title": "Hazardous drug use, unspecified" }, { "code": "6C4Z", "title": "Disorders due to substance use, unspecified" }, { "code": "QE11.3", "title": "Hazardous use of cocaine" }, { "code": "QE11.2", "title": "Hazardous use of sedatives, hypnotics or anxiolytics" }, { "code": "QE11.1", "title": "Hazardous use of cannabis" }, { "code": "3B63.1Z", "title": "Acquired thrombocytosis, unspecified" }, { "code": "3B64.Z", "title": "Thrombocytopenia, unspecified" }, { "code": "4B0Z", "title": "Immune system disorders involving white cell lineages, unspecified" }, { "code": "4B03.Z", "title": "Eosinophilia, unspecified" }, { "code": "4B00.1Z", "title": "Neutrophilia, unspecified" } ]
=== ICD-11 CODES FOUND === [QE11.Z] Hazardous drug use, unspecified Also known as: Hazardous drug use, unspecified | Hazardous drug use | chronic drug use NOS | chronic IV substance use | drug use nos [6C4Z] Disorders due to substance use, unspecified Also known as: Disorders due to substance use, unspecified | Disorders due to substance abuse | drug use disorder | Bad trips due to drugs [QE11.3] Hazardous use of cocaine Definition: A pattern of cocaine use that appreciably increases the risk of harmful physical or mental health consequences to the user or to others to an extent that warrants attention and advice from health professionals. The increased risk may be from the frequency of cocaine use, from the amount used on a given occasion, from risky behaviours associated with cocaine use or the context of use, from a harmful route of administration, or from a combination of these. The risk may be related to short-term eff Also known as: Hazardous use of cocaine | cocaine use | intravenous cocaine use | Hazardous use of crack cocaine | crack cocaine use Excludes: Disorders due to use of cocaine [QE11.2] Hazardous use of sedatives, hypnotics or anxiolytics Definition: A pattern of use of sedatives, hypnotics or anxiolytics that appreciably increases the risk of harmful physical or mental health consequences to the user or to others to an extent that warrants attention and advice from health professionals. The increased risk may be from the frequency of use of sedatives, hypnotics or anxiolytics, from the amount used on a given occasion, from risky behaviours associated with use of sedatives, hypnotics or anxiolytics or the context of use, from a harmful route Also known as: Hazardous use of sedatives, hypnotics or anxiolytics | Hazardous use of anxiolytics | Hazardous use of hypnotics | hypnotic use | Hazardous use of sedatives Excludes: Disorders due to use of sedatives, hypnotics or anxiolytics [QE11.1] Hazardous use of cannabis Definition: A pattern of cannabis use that appreciably increases the risk of harmful physical or mental health consequences to the user or to others to an extent that warrants attention and advice from health professionals. The increased risk may be from the frequency of cannabis use, from the amount used on a given occasion, from risky behaviours associated with cannabis use or the context of use, from a harmful route of administration, or from a combination of these. The risk may be related to short-term Also known as: Hazardous use of cannabis | marijuana use | cannabis use Excludes: Disorders due to use of cannabis [3B63.1Z] Acquired thrombocytosis, unspecified Also known as: Acquired thrombocytosis, unspecified | Acquired thrombocytosis | Idiopathic haemorrhagic thrombocythaemia | Essential thrombocythaemia | primary haemorrhagic thrombocythaemia [3B64.Z] Thrombocytopenia, unspecified Also known as: Thrombocytopenia, unspecified | Thrombocytopenia | low platelet count | low platelets | decreased platelets [4B0Z] Immune system disorders involving white cell lineages, unspecified Also known as: Immune system disorders involving white cell lineages, unspecified [4B03.Z] Eosinophilia, unspecified Also known as: Eosinophilia, unspecified | Eosinophilia | Disorders with increased eosinophil counts | Idiopathic hypereosinophilic syndrome [4B00.1Z] Neutrophilia, unspecified Also known as: Neutrophilia, unspecified | Neutrophilia | Disorders with increased neutrophil counts === GRAPH WALKS === --- Walk 1 --- [QE11.Z] Hazardous drug use, unspecified --PARENT--> [QE11] Hazardous drug use Def: A pattern of use of psychoactive substance(s) other than nicotine or alcohol that appreciably increases the risk of harmful physical or mental health consequences to the user or to others to an extent... --CHILD--> [QE11.0] Hazardous use of opioids Def: A pattern of opioid use that appreciably increases the risk of harmful physical or mental health consequences to the user or to others to an extent that warrants attention and advice from health profe... --- Walk 2 --- [QE11.Z] Hazardous drug use, unspecified --PARENT--> [QE11] Hazardous drug use Def: A pattern of use of psychoactive substance(s) other than nicotine or alcohol that appreciably increases the risk of harmful physical or mental health consequences to the user or to others to an extent... --CHILD--> [QE11.1] Hazardous use of cannabis Def: A pattern of cannabis use that appreciably increases the risk of harmful physical or mental health consequences to the user or to others to an extent that warrants attention and advice from health pro... --- Walk 3 --- [6C4Z] Disorders due to substance use, unspecified --PARENT--> [?] 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... --RELATED_TO--> [?] Catatonia induced by substances or medications Def: Catatonia induced by substances or medications is a syndrome of primarily psychomotor disturbances, characterized by the co-occurrence of several symptoms of decreased, increased, or abnormal psychomo... --- Walk 4 --- [6C4Z] Disorders due to substance use, unspecified --PARENT--> [?] 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... --CHILD--> [6C40] Disorders due to use of alcohol Def: Disorders due to use of alcohol are characterised by the pattern and consequences of alcohol use. Alcohol—more specifically termed ethyl alcohol or ethanol—is an intoxicating compound produced by ferm... --- Walk 5 --- [QE11.3] Hazardous use of cocaine Def: A pattern of cocaine use that appreciably increases the risk of harmful physical or mental health consequences to the user or to others to an extent that warrants attention and advice from health prof... --PARENT--> [QE11] Hazardous drug use Def: A pattern of use of psychoactive substance(s) other than nicotine or alcohol that appreciably increases the risk of harmful physical or mental health consequences to the user or to others to an extent... --CHILD--> [QE11.2] Hazardous use of sedatives, hypnotics or anxiolytics Def: A pattern of use of sedatives, hypnotics or anxiolytics that appreciably increases the risk of harmful physical or mental health consequences to the user or to others to an extent that warrants attent... --- Walk 6 --- [QE11.3] Hazardous use of cocaine Def: A pattern of cocaine use that appreciably increases the risk of harmful physical or mental health consequences to the user or to others to an extent that warrants attention and advice from health prof... --EXCLUDES--> [?] Disorders due to use of cocaine Def: Disorders due to use of cocaine are characterised by the pattern and consequences of cocaine use. Cocaine is a compound found in the leaves of the coca plant, Erythroxylum coca, which is indigenous to... --EXCLUDES--> [?] Disorders due to use of stimulants including amphetamines, methamphetamine or methcathinone Def: Disorders due to use of stimulants including amphetamines, methamphetamine or methcathinone are characterised by the pattern and consequences of use of these substances. There is a wide array of natur...
[ "[QE11.Z] Hazardous drug use, unspecified\n --PARENT--> [QE11] Hazardous drug use\n Def: A pattern of use of psychoactive substance(s) other than nicotine or alcohol that appreciably increases the risk of harmful physical or mental health consequences to the user or to others to an extent...\n --CHILD--> [QE11.0] Hazardous use of opioids\n Def: A pattern of opioid use that appreciably increases the risk of harmful physical or mental health consequences to the user or to others to an extent that warrants attention and advice from health profe...", "[QE11.Z] Hazardous drug use, unspecified\n --PARENT--> [QE11] Hazardous drug use\n Def: A pattern of use of psychoactive substance(s) other than nicotine or alcohol that appreciably increases the risk of harmful physical or mental health consequences to the user or to others to an extent...\n --CHILD--> [QE11.1] Hazardous use of cannabis\n Def: A pattern of cannabis use that appreciably increases the risk of harmful physical or mental health consequences to the user or to others to an extent that warrants attention and advice from health pro...", "[6C4Z] Disorders due to substance use, unspecified\n --PARENT--> [?] 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...\n --RELATED_TO--> [?] Catatonia induced by substances or medications\n Def: Catatonia induced by substances or medications is a syndrome of primarily psychomotor disturbances, characterized by the co-occurrence of several symptoms of decreased, increased, or abnormal psychomo...", "[6C4Z] Disorders due to substance use, unspecified\n --PARENT--> [?] 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...\n --CHILD--> [6C40] Disorders due to use of alcohol\n Def: Disorders due to use of alcohol are characterised by the pattern and consequences of alcohol use. Alcohol—more specifically termed ethyl alcohol or ethanol—is an intoxicating compound produced by ferm...", "[QE11.3] Hazardous use of cocaine\n Def: A pattern of cocaine use that appreciably increases the risk of harmful physical or mental health consequences to the user or to others to an extent that warrants attention and advice from health prof...\n --PARENT--> [QE11] Hazardous drug use\n Def: A pattern of use of psychoactive substance(s) other than nicotine or alcohol that appreciably increases the risk of harmful physical or mental health consequences to the user or to others to an extent...\n --CHILD--> [QE11.2] Hazardous use of sedatives, hypnotics or anxiolytics\n Def: A pattern of use of sedatives, hypnotics or anxiolytics that appreciably increases the risk of harmful physical or mental health consequences to the user or to others to an extent that warrants attent...", "[QE11.3] Hazardous use of cocaine\n Def: A pattern of cocaine use that appreciably increases the risk of harmful physical or mental health consequences to the user or to others to an extent that warrants attention and advice from health prof...\n --EXCLUDES--> [?] Disorders due to use of cocaine\n Def: Disorders due to use of cocaine are characterised by the pattern and consequences of cocaine use. Cocaine is a compound found in the leaves of the coca plant, Erythroxylum coca, which is indigenous to...\n --EXCLUDES--> [?] Disorders due to use of stimulants including amphetamines, methamphetamine or methcathinone\n Def: Disorders due to use of stimulants including amphetamines, methamphetamine or methcathinone are characterised by the pattern and consequences of use of these substances. There is a wide array of natur..." ]
QE11.Z
Hazardous drug use, unspecified
[ { "from_icd11": "QE11.Z", "icd10_code": "Z722", "icd10_title": "" }, { "from_icd11": "6C4Z", "icd10_code": "F1910", "icd10_title": "Other psychoactive substance abuse, uncomplicated" }, { "from_icd11": "6C4Z", "icd10_code": "F1911", "icd10_title": "Other psychoactive substance abuse, in remission" }, { "from_icd11": "6C4Z", "icd10_code": "F19129", "icd10_title": "Other psychoactive substance abuse with intoxication, unspecified" }, { "from_icd11": "6C4Z", "icd10_code": "F19121", "icd10_title": "Other psychoactive substance abuse with intoxication delirium" }, { "from_icd11": "6C4Z", "icd10_code": "F1920", "icd10_title": "Other psychoactive substance dependence, uncomplicated" }, { "from_icd11": "6C4Z", "icd10_code": "F19239", "icd10_title": "Other psychoactive substance dependence with withdrawal, unspecified" }, { "from_icd11": "6C4Z", "icd10_code": "F1914", "icd10_title": "Other psychoactive substance abuse with psychoactive substance-induced mood disorder" }, { "from_icd11": "6C4Z", "icd10_code": "F1921", "icd10_title": "Other psychoactive substance dependence, in remission" }, { "from_icd11": "6C4Z", "icd10_code": "F19221", "icd10_title": "Other psychoactive substance dependence with intoxication delirium" }, { "from_icd11": "6C4Z", "icd10_code": "F19180", "icd10_title": "Other psychoactive substance abuse with psychoactive substance-induced anxiety disorder" }, { "from_icd11": "6C4Z", "icd10_code": "F1924", "icd10_title": "Other psychoactive substance dependence with psychoactive substance-induced mood disorder" }, { "from_icd11": "6C4Z", "icd10_code": "F1917", "icd10_title": "Other psychoactive substance abuse with psychoactive substance-induced persisting dementia" }, { "from_icd11": "6C4Z", "icd10_code": "F19229", "icd10_title": "Other psychoactive substance dependence with intoxication, unspecified" }, { "from_icd11": "6C4Z", "icd10_code": "F1919", "icd10_title": "Other psychoactive substance abuse with unspecified psychoactive substance-induced disorder" } ]
Z722
Objective tests viz (Brainstem evoked response audiometry, Otoacoustic emissions, Immitamce audiometry, and Auditory steady-state response) confirmed the diagnosis of bilateral severe to profound hearing loss. During the hearing aid fitting sessions, optimum responses were not observable with any analog or digital aid. Hence, the subject had been enrolled for diagnostic therapy sessions with digital hearing aids. He would frequently throw his hearing aids, and his parents had to shell out a lot of money to repair and maintain the aids. The psychiatrist's opinion helped to manage ADHD (Methylphenidate was prescribed). At the age of 5, a senior surgeon carried out a successful cochlear implant surgery with Nucleus CI 24 RE (ST) using a round window technique. Intraoperative NRT documented on electrodes 1-18 only. Following "switch on," frequent mapping sessions were required to establish conditioned MAPs. Only the father of the subject attended regular sessions and was highly cooperative. The child accepted the cochlear implant and wore it for approximately 5-6 hours a day. He started comprehending 2-3 word meaningful verbal commands and expressed himself through a few words and phrases along with rudimentary gestures ( Table 2 - 4 ). However, even after one year of auditory verbal therapy, the adequate benefit could not be achieved. He is presently using both oral and manual modes of communication.
4.011719
0.956543
sec[2]/p[18]
en
0.999996
34692575
https://doi.org/10.22038/ijorl.2021.48909.2621
[ "hearing", "sessions", "aids", "response", "audiometry", "auditory", "digital", "subject", "cochlear", "implant" ]
[ { "code": "AB52", "title": "Deafness not otherwise specified" }, { "code": "QA00.7", "title": "Examination of ears and hearing" }, { "code": "MC4Y", "title": "Other specified symptoms or signs involving the ear or mastoid process" }, { "code": "AB54", "title": "Presbycusis" }, { "code": "AB5Z", "title": "Disorders with hearing impairment, unspecified" }, { "code": "QB9Y", "title": "Other specified contact with health services for nonsurgical interventions not involving devices" }, { "code": "QB96", "title": "Contact with health services for radiotherapy session" }, { "code": "QB97", "title": "Contact with health services for chemotherapy session for neoplasm" }, { "code": "1C62.3Z", "title": "HIV disease clinical stage 4 without mention of tuberculosis or malaria, unspecified" }, { "code": "KA62.6", "title": "Congenital human immunodeficiency virus infection" } ]
=== ICD-11 CODES FOUND === [AB52] Deafness not otherwise specified Also known as: Deafness not otherwise specified | deaf | hearing loss NOS | hearing impairment | hearing loss [QA00.7] Examination of ears and hearing Also known as: Examination of ears and hearing | examination of ear | hearing examination | hearing test [MC4Y] Other specified symptoms or signs involving the ear or mastoid process Also known as: Other specified symptoms or signs involving the ear or mastoid process | Hearing complaint | Fear of ear disease [AB54] Presbycusis Definition: The term presbycusis refers to sensorineural hearing impairment in elderly individuals. Characteristically, presbycusis involves bilateral high-frequency hearing loss associated with difficulty in speech discrimination and central auditory processing of information. Also known as: Presbycusis | Presbyacusia | age-related hearing loss | senile deafness | hard of hearing Includes: Presbyacusia [AB5Z] Disorders with hearing impairment, unspecified Also known as: Disorders with hearing impairment, unspecified | disorders with hearing loss [QB9Y] Other specified contact with health services for nonsurgical interventions not involving devices Also known as: Other specified contact with health services for nonsurgical interventions not involving devices | Chemotherapy other than for neoplasm | admission for chemotherapy administration other than for neoplasm | chemotherapy regimen other than for neoplasm | drug therapy other than for neoplasm [QB96] Contact with health services for radiotherapy session Also known as: Contact with health services for radiotherapy session | admission for radiotherapy [QB97] Contact with health services for chemotherapy session for neoplasm Also known as: Contact with health services for chemotherapy session for neoplasm | antineoplastic chemotherapy regimen | cancer chemotherapy regimen | maintenance chemotherapy for neoplasm | neoplasm chemotherapy [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] [KA62.6] Congenital human immunodeficiency virus infection Definition: A disease affecting neonates, caused by an infection with human immunodeficiency virus in utero. Transmission is by vertical transmission. Confirmation is by identification of human immunodeficiency virus in the neonate. Also known as: Congenital human immunodeficiency virus infection | congenital HIV - [human immunodeficiency virus] infection | congenital AIDS === GRAPH WALKS === --- Walk 1 --- [AB52] Deafness not otherwise specified --PARENT--> [?] Disorders with hearing impairment --EXCLUDES--> [?] Otosclerosis Def: Otosclerosis is a genetically mediated metabolic bone disease that affects the otic capsule and stapes. It is an autosomal dominant disorder with varying penetrance and expressivity. Usually symptomat... --- Walk 2 --- [AB52] Deafness not otherwise specified --PARENT--> [?] Disorders with hearing impairment --PARENT--> [10] Diseases of the ear or mastoid process Def: This chapter contains diseases of the ear and diseases of the mastoid process.... --- Walk 3 --- [QA00.7] Examination of ears and hearing --PARENT--> [QA00] General examination or investigation of persons without complaint or reported diagnosis --EXCLUDES--> [?] Examination or encounter for administrative purposes --- Walk 4 --- [QA00.7] Examination of ears and hearing --PARENT--> [QA00] General examination or investigation of persons without complaint or reported diagnosis --EXCLUDES--> [?] Examination or encounter for administrative purposes --- Walk 5 --- [MC4Y] Other specified symptoms or signs involving the ear or mastoid process --PARENT--> [?] Symptoms or signs involving the ear or mastoid process --CHILD--> [MC41] Tinnitus Def: A nonspecific symptom of hearing disorder characterised by the sensation of buzzing, ringing, clicking, pulsations, and other noises in the ear in the absence of appropriate corresponding external sti... --- Walk 6 --- [MC4Y] Other specified symptoms or signs involving the ear or mastoid process --PARENT--> [?] Symptoms or signs involving the ear or mastoid process --CHILD--> [MC41] Tinnitus Def: A nonspecific symptom of hearing disorder characterised by the sensation of buzzing, ringing, clicking, pulsations, and other noises in the ear in the absence of appropriate corresponding external sti...
[ "[AB52] Deafness not otherwise specified\n --PARENT--> [?] Disorders with hearing impairment\n --EXCLUDES--> [?] Otosclerosis\n Def: Otosclerosis is a genetically mediated metabolic bone disease that affects the otic capsule and stapes. It is an autosomal dominant disorder with varying penetrance and expressivity. Usually symptomat...", "[AB52] Deafness not otherwise specified\n --PARENT--> [?] Disorders with hearing impairment\n --PARENT--> [10] Diseases of the ear or mastoid process\n Def: This chapter contains diseases of the ear and diseases of the mastoid process....", "[QA00.7] Examination of ears and hearing\n --PARENT--> [QA00] General examination or investigation of persons without complaint or reported diagnosis\n --EXCLUDES--> [?] Examination or encounter for administrative purposes", "[QA00.7] Examination of ears and hearing\n --PARENT--> [QA00] General examination or investigation of persons without complaint or reported diagnosis\n --EXCLUDES--> [?] Examination or encounter for administrative purposes", "[MC4Y] Other specified symptoms or signs involving the ear or mastoid process\n --PARENT--> [?] Symptoms or signs involving the ear or mastoid process\n --CHILD--> [MC41] Tinnitus\n Def: A nonspecific symptom of hearing disorder characterised by the sensation of buzzing, ringing, clicking, pulsations, and other noises in the ear in the absence of appropriate corresponding external sti...", "[MC4Y] Other specified symptoms or signs involving the ear or mastoid process\n --PARENT--> [?] Symptoms or signs involving the ear or mastoid process\n --CHILD--> [MC41] Tinnitus\n Def: A nonspecific symptom of hearing disorder characterised by the sensation of buzzing, ringing, clicking, pulsations, and other noises in the ear in the absence of appropriate corresponding external sti..." ]
AB52
Deafness not otherwise specified
[ { "from_icd11": "AB52", "icd10_code": "H9190", "icd10_title": "Unspecified hearing loss, unspecified ear" }, { "from_icd11": "AB52", "icd10_code": "H9193", "icd10_title": "Unspecified hearing loss, bilateral" }, { "from_icd11": "QA00.7", "icd10_code": "Z011", "icd10_title": "Encounter for examination of ears and hearing" }, { "from_icd11": "AB54", "icd10_code": "H9113", "icd10_title": "Presbycusis, bilateral" }, { "from_icd11": "AB54", "icd10_code": "H9110", "icd10_title": "Presbycusis, unspecified ear" }, { "from_icd11": "AB54", "icd10_code": "H911", "icd10_title": "Presbycusis" }, { "from_icd11": "AB5Z", "icd10_code": "H9192", "icd10_title": "Unspecified hearing loss, left ear" }, { "from_icd11": "AB5Z", "icd10_code": "H9191", "icd10_title": "Unspecified hearing loss, right ear" }, { "from_icd11": "AB5Z", "icd10_code": "H9011", "icd10_title": "Conductive hearing loss, unilateral, right ear, with unrestricted hearing on the contralateral side" }, { "from_icd11": "AB5Z", "icd10_code": "H918X3", "icd10_title": "Other specified hearing loss, bilateral" }, { "from_icd11": "AB5Z", "icd10_code": "H918X9", "icd10_title": "Other specified hearing loss, unspecified ear" }, { "from_icd11": "AB5Z", "icd10_code": "H918X2", "icd10_title": "Other specified hearing loss, left ear" }, { "from_icd11": "AB5Z", "icd10_code": "H918X1", "icd10_title": "Other specified hearing loss, right ear" }, { "from_icd11": "AB5Z", "icd10_code": "H9012", "icd10_title": "Conductive hearing loss, unilateral, left ear, with unrestricted hearing on the contralateral side" }, { "from_icd11": "AB5Z", "icd10_code": "H913", "icd10_title": "Deaf nonspeaking, not elsewhere classified" } ]
H9190
Unspecified hearing loss, unspecified ear
In this study, the patient’s shoulder joint pathology was insidious, and no apparent acute gout episodes occurred during the entire course of the disease; the condition mainly manifested as chronic arthritis, with right shoulder pain, weakness, and limited mobility. Although the patient had a history of gout, there had been no gout attacks in the shoulder joint; the attacks were mainly manifested in the bilateral feet. Additionally, it was found that the left shoulder joint was also affected by a gouty attack. However, there were no clinical symptoms, which caused some confusion and challenges regarding the diagnosis and treatment. The possibility of gouty arthritis was not initially considered. The patient had a long history of gout, with 2–3 attacks per year, mainly manifested in the bilateral feet, but there were no obvious gout attacks in other parts of the body. Only colchicine was taken orally during the gout attack periods to relieve the symptoms. The patient did not receive an effective and systematic treatment of gout. We believe that the severe destruction of the glenoid was related to an unhealthy diet and the lack of effective and systematic treatment. With effective therapy earlier in the disease process, severe bone destruction of the shoulder bone tissue can be avoided. This condition can lead to significant debilitation in patients if not identified early and managed appropriately.
4.050781
0.887207
sec[2]/p[4]
en
0.999997
33845812
https://doi.org/10.1186/s12891-021-04217-5
[ "gout", "shoulder", "attacks", "joint", "mainly", "manifested", "effective", "this", "arthritis", "feet" ]
[ { "code": "FA25.2Z", "title": "Gout, unspecified" }, { "code": "FA25", "title": "Gout" }, { "code": "FA25.0", "title": "Primary gout" }, { "code": "FA25.10", "title": "Lead-induced gout" }, { "code": "FA25.11", "title": "Drug-induced gout" }, { "code": "ME86.D0", "title": "Shoulder syndrome" }, { "code": "FB53.Z", "title": "Shoulder lesions, unspecified" }, { "code": "NC10.Y&XA2ND5", "title": "Haematoma of shoulder" }, { "code": "FB53.0", "title": "Adhesive capsulitis of shoulder" }, { "code": "JB06.0", "title": "Obstructed labour due to shoulder dystocia" } ]
=== ICD-11 CODES FOUND === [FA25.2Z] Gout, unspecified Also known as: Gout, unspecified | Gout without specification whether primary or secondary | gout NOS | gouty | gouty diathesis [FA25] Gout Definition: Gout is an acute or chronic arthropathy resulting from deposition of monosodium urate monohydrate crystals in joint tissues. It is strongly associated with hyperuricaemia, which may be secondary to certain drugs, poisons or lymphoproliferative disorders. Gout is definitively diagnosed by demonstration of urate crystals in aspirated synovial fluid in the absence of an alternative aetiology for arthritis. It may be associated with focal urate deposition in skin and subcutaneous tissue (tophaceous Also known as: Gout Excludes: Hyperuricaemia without signs of inflammatory arthritis or tophaceous disease [FA25.0] Primary gout Definition: Primary gout refers to those cases that appear to be innate, that are neither secondary to another acquired disorder nor a subordinate manifestation of an inborn error that leads initially to a major disease unlike gout. Although some cases of primary gout have a genetic basis, others do not. Also known as: Primary gout | idiopathic gout | articular gout | idiopathic gout, unspecified site | gouty arthritis Includes: Gouty bursitis | Gouty arthropathy [FA25.10] Lead-induced gout Also known as: Lead-induced gout | gout due to lead poisoning | gout secondary to lead | lead gout | saturnine gout [FA25.11] Drug-induced gout Also known as: Drug-induced gout | drug-induced gout, unspecified site | gout secondary to drug | medicament-induced gout | Acute drug-induced gout [ME86.D0] Shoulder syndrome Definition: A shoulder syndrome is defined by shoulder pain with one or more of the following problems: limitations of movement, local tenderness, crepitus or periarticular calcification in imaging. Also known as: Shoulder syndrome Excludes: Arthropathies | Shoulder lesions | Chronic primary musculoskeletal pain [FB53.Z] Shoulder lesions, unspecified Also known as: Shoulder lesions, unspecified | Shoulder lesions | enthesopathy of shoulder region | lesion of shoulder [FB53.0] Adhesive capsulitis of shoulder Definition: This is a condition characterised by spontaneous onset of shoulder pain accompanied by progressive loss of active and passive ranges of motion. Also known as: Adhesive capsulitis of shoulder | Frozen shoulder | pericapsulitis of shoulder | duplay bursitis | adhesive shoulder peritendinitis Includes: Frozen shoulder [JB06.0] Obstructed labour due to shoulder dystocia Also known as: Obstructed labour due to shoulder dystocia | obstructed delivery due to impacted shoulder | impacted shoulder causing obstructed labour | labour obstructed by impacted shoulders | labour obstructed by shoulder dystocia or impaction Includes: Impacted shoulders === GRAPH WALKS === --- Walk 1 --- [FA25.2Z] Gout, unspecified --PARENT--> [FA25.2] Gout without specification whether primary or secondary --CHILD--> [FA25.20] Tophaceous gout Def: Tophi are precipitates of monosodium urate in the tissues of patients with hyperuricaemia and may be associated with other manifestations of hyperuricaemia including gouty arthropathy. They present pa... --- Walk 2 --- [FA25.2Z] Gout, unspecified --PARENT--> [FA25.2] Gout without specification whether primary or secondary --CHILD--> [FA25.20] Tophaceous gout Def: Tophi are precipitates of monosodium urate in the tissues of patients with hyperuricaemia and may be associated with other manifestations of hyperuricaemia including gouty arthropathy. They present pa... --- Walk 3 --- [FA25] Gout Def: Gout is an acute or chronic arthropathy resulting from deposition of monosodium urate monohydrate crystals in joint tissues. It is strongly associated with hyperuricaemia, which may be secondary to ce... --CHILD--> [FA25.1] Secondary gout Def: Secondary gout refers to those cases that develop during the course of another disease, or as a consequence of treatment with drugs. Secondary gout is associated with increased purine biosynthesis de ... --CHILD--> [FA25.12] Gouty arthropathy due to enzyme defects or other inherited disorders --- Walk 4 --- [FA25] Gout Def: Gout is an acute or chronic arthropathy resulting from deposition of monosodium urate monohydrate crystals in joint tissues. It is strongly associated with hyperuricaemia, which may be secondary to ce... --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 --- [FA25.0] Primary gout Def: Primary gout refers to those cases that appear to be innate, that are neither secondary to another acquired disorder nor a subordinate manifestation of an inborn error that leads initially to a major ... --PARENT--> [FA25] Gout Def: Gout is an acute or chronic arthropathy resulting from deposition of monosodium urate monohydrate crystals in joint tissues. It is strongly associated with hyperuricaemia, which may be secondary to ce... --EXCLUDES--> [?] Hyperuricaemia without signs of inflammatory arthritis or tophaceous disease Def: This refers to a level of uric acid in the blood that is abnormally high. This diagnosis is without signs of inflammatory arthritis and tophaceous disease.... --- Walk 6 --- [FA25.0] Primary gout Def: Primary gout refers to those cases that appear to be innate, that are neither secondary to another acquired disorder nor a subordinate manifestation of an inborn error that leads initially to a major ... --PARENT--> [FA25] Gout Def: Gout is an acute or chronic arthropathy resulting from deposition of monosodium urate monohydrate crystals in joint tissues. It is strongly associated with hyperuricaemia, which may be secondary to ce... --EXCLUDES--> [?] Hyperuricaemia without signs of inflammatory arthritis or tophaceous disease Def: This refers to a level of uric acid in the blood that is abnormally high. This diagnosis is without signs of inflammatory arthritis and tophaceous disease....
[ "[FA25.2Z] Gout, unspecified\n --PARENT--> [FA25.2] Gout without specification whether primary or secondary\n --CHILD--> [FA25.20] Tophaceous gout\n Def: Tophi are precipitates of monosodium urate in the tissues of patients with hyperuricaemia and may be associated with other manifestations of hyperuricaemia including gouty arthropathy. They present pa...", "[FA25.2Z] Gout, unspecified\n --PARENT--> [FA25.2] Gout without specification whether primary or secondary\n --CHILD--> [FA25.20] Tophaceous gout\n Def: Tophi are precipitates of monosodium urate in the tissues of patients with hyperuricaemia and may be associated with other manifestations of hyperuricaemia including gouty arthropathy. They present pa...", "[FA25] Gout\n Def: Gout is an acute or chronic arthropathy resulting from deposition of monosodium urate monohydrate crystals in joint tissues. It is strongly associated with hyperuricaemia, which may be secondary to ce...\n --CHILD--> [FA25.1] Secondary gout\n Def: Secondary gout refers to those cases that develop during the course of another disease, or as a consequence of treatment with drugs. Secondary gout is associated with increased purine biosynthesis de ...\n --CHILD--> [FA25.12] Gouty arthropathy due to enzyme defects or other inherited disorders", "[FA25] Gout\n Def: Gout is an acute or chronic arthropathy resulting from deposition of monosodium urate monohydrate crystals in joint tissues. It is strongly associated with hyperuricaemia, which may be secondary to ce...\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...", "[FA25.0] Primary gout\n Def: Primary gout refers to those cases that appear to be innate, that are neither secondary to another acquired disorder nor a subordinate manifestation of an inborn error that leads initially to a major ...\n --PARENT--> [FA25] Gout\n Def: Gout is an acute or chronic arthropathy resulting from deposition of monosodium urate monohydrate crystals in joint tissues. It is strongly associated with hyperuricaemia, which may be secondary to ce...\n --EXCLUDES--> [?] Hyperuricaemia without signs of inflammatory arthritis or tophaceous disease\n Def: This refers to a level of uric acid in the blood that is abnormally high. This diagnosis is without signs of inflammatory arthritis and tophaceous disease....", "[FA25.0] Primary gout\n Def: Primary gout refers to those cases that appear to be innate, that are neither secondary to another acquired disorder nor a subordinate manifestation of an inborn error that leads initially to a major ...\n --PARENT--> [FA25] Gout\n Def: Gout is an acute or chronic arthropathy resulting from deposition of monosodium urate monohydrate crystals in joint tissues. It is strongly associated with hyperuricaemia, which may be secondary to ce...\n --EXCLUDES--> [?] Hyperuricaemia without signs of inflammatory arthritis or tophaceous disease\n Def: This refers to a level of uric acid in the blood that is abnormally high. This diagnosis is without signs of inflammatory arthritis and tophaceous disease...." ]
FA25.2Z
Gout, unspecified
[ { "from_icd11": "FA25.2Z", "icd10_code": "M109", "icd10_title": "Gout, unspecified" }, { "from_icd11": "FA25", "icd10_code": "M10", "icd10_title": "Gout" }, { "from_icd11": "FA25", "icd10_code": "M1A9XX0", "icd10_title": "Chronic gout, unspecified, without tophus (tophi)" }, { "from_icd11": "FA25.0", "icd10_code": "M10072", "icd10_title": "Idiopathic gout, left ankle and foot" }, { "from_icd11": "FA25.0", "icd10_code": "M10062", "icd10_title": "Idiopathic gout, left knee" }, { "from_icd11": "FA25.0", "icd10_code": "M1000", "icd10_title": "Idiopathic gout, unspecified site" }, { "from_icd11": "FA25.0", "icd10_code": "M10061", "icd10_title": "Idiopathic gout, right knee" }, { "from_icd11": "FA25.0", "icd10_code": "M10071", "icd10_title": "Idiopathic gout, right ankle and foot" }, { "from_icd11": "FA25.0", "icd10_code": "M1009", "icd10_title": "Idiopathic gout, multiple sites" }, { "from_icd11": "FA25.0", "icd10_code": "M10032", "icd10_title": "Idiopathic gout, left wrist" }, { "from_icd11": "FA25.0", "icd10_code": "M10069", "icd10_title": "Idiopathic gout, unspecified knee" }, { "from_icd11": "FA25.0", "icd10_code": "M10022", "icd10_title": "Idiopathic gout, left elbow" }, { "from_icd11": "FA25.0", "icd10_code": "M10049", "icd10_title": "Idiopathic gout, unspecified hand" }, { "from_icd11": "FA25.0", "icd10_code": "M10031", "icd10_title": "Idiopathic gout, right wrist" }, { "from_icd11": "FA25.0", "icd10_code": "M10042", "icd10_title": "Idiopathic gout, left hand" } ]
M109
Gout, unspecified
A 61-year-old Japanese man visited our department for a verrucous formation on his lip that was growing rapidly and invading his palate . He also showed verrucous vegetation characterized by pigmentation, and a blackish brown mass with pruritus gradually developed on his axilla, posterior neck, and face. He had a history of hypertension, hyperuricemia, hyperlipidemia, gastrectomy and cholecystectomy for gastric cancer and was actively receiving chemotherapy for the treatment of multiple metastases. We diagnosed malignant acanthosis nigricans and verruca vulgaris. We intended to perform a skin biopsy of a patient with verrucous vulgaris to exclude verrucous carcinoma, squamous papilloma, condyloma acuminatum, and multifocal epithelial hyperplasia, but we could not obtain consent from the patient. The verruca was treated with cryotherapy without any response. Due to the serious phenotypes of his skin manifestations, we were anxious about the patient's immune status; however, his immune condition had been evaluated as “normal” by his physician on the basis of laboratory data including a complete blood count (CBC). Although his neutrophil function in phagocytosis and sterilization fell within the normal range, his natural killer (NK) cell activity was 0.3% (normal range: 8.9–29.5%). We issued a warning about his immunosuppressed status, but the patient died due to pneumonia and multiple organ failure.
3.912109
0.980957
sec[1]/sec[0]/p[0]
en
0.999997
33343946
https://doi.org/10.1155/2020/6682694
[ "verrucous", "multiple", "verruca", "vulgaris", "skin", "about", "immune", "status", "range", "japanese" ]
[ { "code": "DA01.00", "title": "Oral leukoplakia" }, { "code": "1B12.8", "title": "Cutaneous tuberculosis" }, { "code": "1F24", "title": "Chromoblastomycosis" }, { "code": "2C31.0", "title": "Verrucous squamous cell carcinoma of skin" }, { "code": "LC52", "title": "Complex or combined developmental vascular malformations involving the skin" }, { "code": "6B64", "title": "Dissociative identity disorder" }, { "code": "JA80.Z", "title": "Maternal care related to unspecified multiple gestation" }, { "code": "QA46.Z", "title": "Outcome of delivery, unspecified" }, { "code": "8A40.Z", "title": "Multiple sclerosis, unspecified" }, { "code": "ND31", "title": "Open wounds involving multiple body regions" } ]
=== ICD-11 CODES FOUND === [DA01.00] Oral leukoplakia Definition: Leukoplakia is a condition where areas of keratosis appear as adherent white patches on the mucous membranes of the oral cavity. Leukoplakia may affect other gastrointestinal tract mucosal sites, or mucosal surfaces of the urinary tract and genitals. Also known as: Oral leukoplakia | Leukoplakia of gingiva | leukoplakia of oral epithelium | leucoplakia of oral mucosa | leukokeratosis of oral mucosa Includes: Leukoplakia of gingiva Excludes: Hairy leukoplakia [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 [1F24] Chromoblastomycosis Definition: Chromoblastomycosis is a chronic fungal infection of the skin and subcutaneous tissues caused by a variety of pigmented fungi including Phialophora verrucosa, Fonsecaea pedrosoi, Fonsecaea compacta and Cladophialophora carrionii, which can be found in soil and wood. The infection usually follows trauma, such as a puncture from a splinter of wood and tends to affect exposed sites such as the feet and ankles. Chromoblastomycosis manifests initially as a warty papule which slowly enlarges to form a Also known as: Chromoblastomycosis | Verrucous dermatitis | Fonseca disease | Pedroso disease | chromomycosis [2C31.0] Verrucous squamous cell carcinoma of skin Definition: Verrucous squamous cell carcinoma is a rare variant of well-differentiated squamous cell carcinoma with low malignant potential. It occurs principally on the glans and prepuce of the penis and on the sole of the foot. Also known as: Verrucous squamous cell carcinoma of skin | Verrucous carcinoma of skin | Verrucous squamous cell carcinoma of penis | Verrucous carcinoma of penis | Giant condyloma acuminatum of Buschke and Löwenstein involving penis Excludes: Verrucous squamous cell carcinoma of vulva [LC52] Complex or combined developmental vascular malformations involving the skin Also known as: Complex or combined developmental vascular malformations involving the skin | Cutis marmorata telangiectatica congenita | Congenital phlebectasia | Reticulate vascular naevus | CMTC - [Cutis marmorata telangiectatica congenita] [6B64] Dissociative identity disorder Definition: Dissociative identity disorder is characterised by disruption of identity in which there are two or more distinct personality states (dissociative identities) associated with marked discontinuities in the sense of self and agency. Each personality state includes its own pattern of experiencing, perceiving, conceiving, and relating to self, the body, and the environment. At least two distinct personality states recurrently take executive control of the individual’s consciousness and functioning i Also known as: Dissociative identity disorder | Multiple personality | Multiple personality disorder [JA80.Z] Maternal care related to unspecified multiple gestation Also known as: Maternal care related to unspecified multiple gestation | Maternal care related to multiple gestation | multiple gestation, unspecified, unspecified trimester | multiple pregnancy | Multiple pregnancy NOS [QA46.Z] Outcome of delivery, unspecified Also known as: Outcome of delivery, unspecified | Outcome of delivery | Multiple birth, unspecified | Single birth, unspecified [8A40.Z] Multiple sclerosis, unspecified Also known as: Multiple sclerosis, unspecified | Multiple sclerosis | cerebrospinal sclerosis | disseminated sclerosis | generalised multiple sclerosis [ND31] Open wounds involving multiple body regions Also known as: Open wounds involving multiple body regions | Open wounds involving head with neck | Open wounds of sites classifiable as open wounds to the head or open wounds of the neck | Nasopharyngeal laceration | Open wounds involving thorax with abdomen, lower back or pelvis Excludes: Traumatic amputations involving multiple body regions === GRAPH WALKS === --- Walk 1 --- [DA01.00] Oral leukoplakia Def: Leukoplakia is a condition where areas of keratosis appear as adherent white patches on the mucous membranes of the oral cavity. Leukoplakia may affect other gastrointestinal tract mucosal sites, or m... --EXCLUDES--> [?] Hairy leukoplakia Def: Oral hairy leukoplakia is a focal epithelial hyperplasia of the oral mucosa associated with Epstein-Barr virus. It is closely associated with HIV and occurs in both immunocompromised and immunocompete... --CHILD--> [?] Hairy leukoplakia of tongue --- Walk 2 --- [DA01.00] Oral leukoplakia Def: Leukoplakia is a condition where areas of keratosis appear as adherent white patches on the mucous membranes of the oral cavity. Leukoplakia may affect other gastrointestinal tract mucosal sites, or m... --EXCLUDES--> [?] Hairy leukoplakia Def: Oral hairy leukoplakia is a focal epithelial hyperplasia of the oral mucosa associated with Epstein-Barr virus. It is closely associated with HIV and occurs in both immunocompromised and immunocompete... --PARENT--> [?] Skin disorders associated with Human immunodeficiency virus infection Def: The skin manifestations of human immunodeficiency virus infection are manifold and are frequently the presenting sign of initial infection or of advanced disease. Other retroviruses, especially HTLV-1... --- Walk 3 --- [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 4 --- [1B12.8] Cutaneous tuberculosis Def: Tuberculosis involving the skin and mucous membranes including lupus vulgaris, scrofuloderma and periorificial tuberculosis.... --PARENT--> [1B12] Tuberculosis of other systems and organs --CHILD--> [1B12.0] Tuberculosis of heart Def: Mycobacterium tuberculosis infection involving the heart and pericardium... --- Walk 5 --- [1F24] Chromoblastomycosis Def: Chromoblastomycosis is a chronic fungal infection of the skin and subcutaneous tissues caused by a variety of pigmented fungi including Phialophora verrucosa, Fonsecaea pedrosoi, Fonsecaea compacta an... --PARENT--> [?] Mycoses --CHILD--> [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... --- Walk 6 --- [1F24] Chromoblastomycosis Def: Chromoblastomycosis is a chronic fungal infection of the skin and subcutaneous tissues caused by a variety of pigmented fungi including Phialophora verrucosa, Fonsecaea pedrosoi, Fonsecaea compacta an... --PARENT--> [?] Mycoses --EXCLUDES--> [?] Hypersensitivity pneumonitis due to organic dust Def: Hypersensitivity pneumonitis due to organic dust is an inflammation of the alveoli, terminal bronchioli and the interstitium within caused by hypersensitivity to inhaled organic dusts, such as allerge...
[ "[DA01.00] Oral leukoplakia\n Def: Leukoplakia is a condition where areas of keratosis appear as adherent white patches on the mucous membranes of the oral cavity. Leukoplakia may affect other gastrointestinal tract mucosal sites, or m...\n --EXCLUDES--> [?] Hairy leukoplakia\n Def: Oral hairy leukoplakia is a focal epithelial hyperplasia of the oral mucosa associated with Epstein-Barr virus. It is closely associated with HIV and occurs in both immunocompromised and immunocompete...\n --CHILD--> [?] Hairy leukoplakia of tongue", "[DA01.00] Oral leukoplakia\n Def: Leukoplakia is a condition where areas of keratosis appear as adherent white patches on the mucous membranes of the oral cavity. Leukoplakia may affect other gastrointestinal tract mucosal sites, or m...\n --EXCLUDES--> [?] Hairy leukoplakia\n Def: Oral hairy leukoplakia is a focal epithelial hyperplasia of the oral mucosa associated with Epstein-Barr virus. It is closely associated with HIV and occurs in both immunocompromised and immunocompete...\n --PARENT--> [?] Skin disorders associated with Human immunodeficiency virus infection\n Def: The skin manifestations of human immunodeficiency virus infection are manifold and are frequently the presenting sign of initial infection or of advanced disease. Other retroviruses, especially HTLV-1...", "[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...", "[1B12.8] Cutaneous tuberculosis\n Def: Tuberculosis involving the skin and mucous membranes including lupus vulgaris, scrofuloderma and periorificial tuberculosis....\n --PARENT--> [1B12] Tuberculosis of other systems and organs\n --CHILD--> [1B12.0] Tuberculosis of heart\n Def: Mycobacterium tuberculosis infection involving the heart and pericardium...", "[1F24] Chromoblastomycosis\n Def: Chromoblastomycosis is a chronic fungal infection of the skin and subcutaneous tissues caused by a variety of pigmented fungi including Phialophora verrucosa, Fonsecaea pedrosoi, Fonsecaea compacta an...\n --PARENT--> [?] Mycoses\n --CHILD--> [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...", "[1F24] Chromoblastomycosis\n Def: Chromoblastomycosis is a chronic fungal infection of the skin and subcutaneous tissues caused by a variety of pigmented fungi including Phialophora verrucosa, Fonsecaea pedrosoi, Fonsecaea compacta an...\n --PARENT--> [?] Mycoses\n --EXCLUDES--> [?] Hypersensitivity pneumonitis due to organic dust\n Def: Hypersensitivity pneumonitis due to organic dust is an inflammation of the alveoli, terminal bronchioli and the interstitium within caused by hypersensitivity to inhaled organic dusts, such as allerge..." ]
DA01.00
Oral leukoplakia
[ { "from_icd11": "DA01.00", "icd10_code": "K1329", "icd10_title": "Other disturbances of oral epithelium, including tongue" }, { "from_icd11": "DA01.00", "icd10_code": "K1321", "icd10_title": "Leukoplakia of oral mucosa, including tongue" }, { "from_icd11": "DA01.00", "icd10_code": "K132", "icd10_title": "Leukoplakia and other disturbances of oral epithelium, including tongue" }, { "from_icd11": "1B12.8", "icd10_code": "A184", "icd10_title": "Tuberculosis of skin and subcutaneous tissue" }, { "from_icd11": "1F24", "icd10_code": "B430", "icd10_title": "Cutaneous chromomycosis" }, { "from_icd11": "1F24", "icd10_code": "B43", "icd10_title": "Chromomycosis and pheomycotic abscess" }, { "from_icd11": "1F24", "icd10_code": "B438", "icd10_title": "Other forms of chromomycosis" }, { "from_icd11": "1F24", "icd10_code": "B439", "icd10_title": "Chromomycosis, unspecified" }, { "from_icd11": "LC52", "icd10_code": "D1802", "icd10_title": "Hemangioma of intracranial structures" }, { "from_icd11": "LC52", "icd10_code": "D1801", "icd10_title": "Hemangioma of skin and subcutaneous tissue" }, { "from_icd11": "LC52", "icd10_code": "D1809", "icd10_title": "Hemangioma of other sites" }, { "from_icd11": "LC52", "icd10_code": "D1803", "icd10_title": "Hemangioma of intra-abdominal structures" }, { "from_icd11": "LC52", "icd10_code": "D1800", "icd10_title": "Hemangioma unspecified site" }, { "from_icd11": "LC52", "icd10_code": "D180", "icd10_title": "Hemangioma" }, { "from_icd11": "LC52", "icd10_code": "Q274", "icd10_title": "Congenital phlebectasia" } ]
K1329
Other disturbances of oral epithelium, including tongue
Case 2 involved a 65-year-old man who underwent TAR and proximal descending aorta replacement with a 26-mm UBE woven graft (Ube Industries, Tokyo, Japan) for type A aortic dissection 12 years ago. CTA revealed an extensive dissected TAAA; the maximum diameters of the descending thoracic and abdominal aortas were 55 mm and 45 mm, respectively. The Adamkiewicz artery was visualized as arising from the 12th intercostal artery. Thoracoabdominal replacement was performed similarly to that performed for the first patient. The descending aorta and Adamkiewicz artery were reconstructed using double-barrel anastomosis and two tubular grafts (24-mm thoracoabdominal J graft), respectively. TEVAR was subsequently performed with 31–200-mm and 31–200-mm Gore CTAG stent grafts (WL Gore, Newark, Delaware, United States) 19 days after the initial operation. No abnormal finding was observed with the postoperative CTA , and no SCI was occurred. The patient was discharged on the 34th postoperative day with no complications. Embolization of type 2 endoleak was performed 38 months after the TEVAR, and the patient are alive 44 months after the operation. Fig. 2 3D-CTA images of case 2 and 3. a The abdominal aorta of case 2 during the preoperative period and after the primary open surgery and hybrid repair; b the abdominal aorta of case 3 during the preoperative period and after the primary open surgery and hybrid repair
3.896484
0.980469
sec[1]/p[1]
en
0.999998
35189912
https://doi.org/10.1186/s13019-022-01764-3
[ "aorta", "descending", "abdominal", "artery", "replacement", "graft", "type", "respectively", "adamkiewicz", "thoracoabdominal" ]
[ { "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": "LB52.1", "title": "Undescended testicle, unilateral" }, { "code": "BD50.4Z", "title": "Abdominal aortic aneurysm, without mention of perforation or rupture" }, { "code": "2C80.Z", "title": "Malignant neoplasms of testis, unspecified" }, { "code": "LB52.2", "title": "Undescended testicle, bilateral" }, { "code": "2E92.4Y", "title": "Other specified benign neoplasm of the large intestine" } ]
=== ICD-11 CODES FOUND === [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 [LB52.1] Undescended testicle, unilateral Definition: The situation in which one of the two testicles in a male has not transitioned from the abdomen, and therefore appears absent from the scrotum. Also known as: Undescended testicle, unilateral | unilateral cryptorchidism | unilateral undescended testis | nondescent unilateral testicle | unilateral cryptorchism [BD50.4Z] Abdominal aortic aneurysm, without mention of perforation or rupture Also known as: Abdominal aortic aneurysm, without mention of perforation or rupture | Abdominal aortic aneurysm | abdomen aneurysm | abdominal aorta aneurysm | aneurysm of abdominal aorta [2C80.Z] Malignant neoplasms of testis, unspecified Also known as: Malignant neoplasms of testis, unspecified | Malignant neoplasms of testis | cancer of testis | testis cancer | malignant neoplasm of testis, NOS [LB52.2] Undescended testicle, bilateral Definition: The situation in which both testicles in a male have not transitioned from the abdomen, and therefore appear absent from the scrotum. Also known as: Undescended testicle, bilateral | bilateral cryptorchidism | bilateral cryptorchism | bilateral nondescent testicle | bilateral undescended testes [2E92.4Y] Other specified benign neoplasm of the large intestine Also known as: Other specified benign neoplasm of the large intestine | Benign neoplasm of appendix | benign tumour of appendix | Benign epithelial tumour of appendix | Hyperplastic polyp of appendix === GRAPH WALKS === --- Walk 1 --- [BD5Z] Diseases of arteries or arterioles, unspecified --PARENT--> [?] Diseases of arteries or arterioles --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 2 --- [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 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... --PARENT--> [?] Congenital anomaly of aortic valve Def: A congenital cardiovascular malformation where the aortic valve is abnormal.... --- 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... --EXCLUDES--> [?] Congenital subaortic stenosis --- Walk 5 --- [BD40.1] Atherosclerosis of aorta --PARENT--> [BD40] Atherosclerotic chronic arterial occlusive disease --CHILD--> [BD40.2] Atherosclerosis of renal artery --- Walk 6 --- [BD40.1] Atherosclerosis of aorta --PARENT--> [BD40] Atherosclerotic chronic arterial occlusive disease --CHILD--> [BD40.1] Atherosclerosis of aorta
[ "[BD5Z] Diseases of arteries or arterioles, unspecified\n --PARENT--> [?] Diseases of arteries or arterioles\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...", "[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. ...", "[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....", "[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", "[BD40.1] Atherosclerosis of aorta\n --PARENT--> [BD40] Atherosclerotic chronic arterial occlusive disease\n --CHILD--> [BD40.2] Atherosclerosis of renal artery", "[BD40.1] Atherosclerosis of aorta\n --PARENT--> [BD40] Atherosclerotic chronic arterial occlusive disease\n --CHILD--> [BD40.1] Atherosclerosis of aorta" ]
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
A 7-year-old boy was taken to the hospital by his parents due to an accidental impact on his abdomen while playing together with his classmates. His physician arranged an abdominal computed tomography (CT) examination for him. In the process of abdominal CT scanning, the examiner found no obvious abnormal signs in his abdomen. However, he accidentally found that the child's lower lobes of right lung had some signs of airway dilatation and mucus retention, and thus the examiner reported these findings responsibly to the doctor in charge. Next, the child was transferred to the respiratory specialist in our hospital and completed a chest high-resolution computed tomography (HRCT) scan. The HRCT revealed multiple dilations and mucus plugs in the right lower lobe bronchus . The dilated trachea was approximately 7 mm in diameter at its widest point. Multiple patchy shadows with ill-defined borders were seen in the right lower lobe, mainly in the medial and posterior basal segments. In addition to that, several well-demarcated, irregular, partial translucent shadows were seen in the left lung. The right pleura was slightly thicker. According to the published guidelines, the child was radiologically diagnosed with bronchiectasis ( 11 ). However, we had admitted the patient without any respiratory symptoms. During auscultation, we only found that the breath sound of the right lower lung was mild decreased.
3.865234
0.980957
sec[1]/p[0]
en
0.999997
PMC9869259
https://doi.org/10.3389/fped.2022.1077878
[ "that", "lung", "abdomen", "abdominal", "computed", "tomography", "examiner", "however", "mucus", "respiratory" ]
[ { "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": "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 === [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 [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 --- [8A80.Z] Migraine, unspecified --PARENT--> [8A80] Migraine Def: A primary headache disorder, in most cases episodic. Disabling attacks lasting 4-72 hours are characterised by moderate or severe headache, usually accompanied by nausea, vomiting and/or photophobia a... --EXCLUDES--> [?] Headache, not elsewhere classified Def: Headache with characteristic features suggesting that it is a unique diagnostic entity, a finding or complaint, but not fulfilling criteria for any of the headache disorders described above.... --- Walk 2 --- [8A80.Z] Migraine, unspecified --PARENT--> [8A80] Migraine Def: A primary headache disorder, in most cases episodic. Disabling attacks lasting 4-72 hours are characterised by moderate or severe headache, usually accompanied by nausea, vomiting and/or photophobia a... --EXCLUDES--> [?] Headache, not elsewhere classified Def: Headache with characteristic features suggesting that it is a unique diagnostic entity, a finding or complaint, but not fulfilling criteria for any of the headache disorders described above.... --- Walk 3 --- [QA76] Medication or substance that is known to be an allergen without injury or harm Def: Medication that has previously been identified as an allergen to the patient is administered, but does not result in injury or harm.... --EXCLUDES--> [?] Medication or substance that is known to be an allergen, as mode of injury or harm --PARENT--> [?] Mode of injury or harm associated with exposure to a drug, medicament or biological substance --- Walk 4 --- [QA76] Medication or substance that is known to be an allergen without injury or harm Def: Medication that has previously been identified as an allergen to the patient is administered, but does not result in injury or harm.... --PARENT--> [?] Circumstances associated with exposure to a drug, medicament or biological substance influencing the episode of care without injury or harm --EXCLUDES--> [?] 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 --EXCLUDES--> [?] Headache, not elsewhere classified\n Def: Headache with characteristic features suggesting that it is a unique diagnostic entity, a finding or complaint, but not fulfilling criteria for any of the headache disorders described above....", "[8A80.Z] Migraine, unspecified\n --PARENT--> [8A80] Migraine\n Def: A primary headache disorder, in most cases episodic. Disabling attacks lasting 4-72 hours are characterised by moderate or severe headache, usually accompanied by nausea, vomiting and/or photophobia a...\n --EXCLUDES--> [?] Headache, not elsewhere classified\n Def: Headache with characteristic features suggesting that it is a unique diagnostic entity, a finding or complaint, but not fulfilling criteria for any of the headache disorders described above....", "[QA76] Medication or substance that is known to be an allergen without injury or harm\n Def: Medication that has previously been identified as an allergen to the patient is administered, but does not result in injury or harm....\n --EXCLUDES--> [?] Medication or substance that is known to be an allergen, as mode of injury or harm\n --PARENT--> [?] Mode of injury or harm associated with exposure to a drug, medicament or biological substance", "[QA76] Medication or substance that is known to be an allergen without injury or harm\n Def: Medication that has previously been identified as an allergen to the patient is administered, but does not result in injury or harm....\n --PARENT--> [?] Circumstances associated with exposure to a drug, medicament or biological substance influencing the episode of care without injury or harm\n --EXCLUDES--> [?] 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
The incidence of thyroid eye disease (TED) is 2.9 and 16.0 cases per 10,000 population per year among males and females, respectively. The higher prevalence in females is associated with a higher incidence of hyperthyroidism in them . Unilateral TED is seen in nearly 4-14% of cases. However, a visible and palpable lump, strictly unilateral or gross asymmetric eye involvement, non-axial (eccentric) proptosis, a lack of lid retraction or lid lag on downward gaze, or weakened muscle function (suggestive of tendon involvement) are the critical features of non-TED mediated ocular involvement, as in our patient . Initially, our patient was diagnosed with euthyroid ophthalmopathy and was treated with prednisone and teprotumumab; proptosis significantly decreased from 30 mm to 20 mm on discharge. The OPTIC-X study has shown that teprotumumab, administered once every three weeks, effectively reduced proptosis and diplopia . Our patient, after an initial improvement in vision, diplopia, and proptosis, deteriorated, following which a biopsy was done, which revealed MALT lymphoma. According to a report, the median latency between the diagnosis of thyroid orbitopathy and the development of periocular lymphoma in patients was 17.5 years . According to another case report, the time to diagnosis was five years . Our patient was diagnosed with lymphoma within two years of the diagnosis of euthyroid ophthalmopathy.
4.085938
0.862793
sec[2]/p[1]
en
0.999998
PMC10011929
https://doi.org/10.7759/cureus.34885
[ "proptosis", "involvement", "lymphoma", "incidence", "thyroid", "cases", "females", "higher", "diagnosed", "euthyroid" ]
[ { "code": "9A20.00", "title": "Outward displacement of eyeball" }, { "code": "LA10.Y", "title": "Other specified structural developmental anomalies of ocular globes" }, { "code": "DA0B.5", "title": "Developmental or acquired deformities or conditions of gingiva" }, { "code": "4B2Y", "title": "Other specified disorders involving the immune system" }, { "code": "4A42.Z", "title": "Systemic sclerosis, unspecified" }, { "code": "KC20.Z", "title": "Conditions involving the umbilical cord, unspecified" }, { "code": "ED3Y", "title": "Cutaneous involvement in other specified neurological condition" }, { "code": "2B33.5", "title": "Malignant lymphoma, not elsewhere classified" }, { "code": "2A80.Z", "title": "Follicular lymphoma, unspecified" }, { "code": "2B30.Z", "title": "Hodgkin lymphoma, unspecified" } ]
=== ICD-11 CODES FOUND === [9A20.00] Outward displacement of eyeball Also known as: Outward displacement of eyeball | Proptosis | Exophthalmos | Exorbitism | Exophthalmic conditions Includes: Proptosis | Exophthalmos [LA10.Y] Other specified structural developmental anomalies of ocular globes Also known as: Other specified structural developmental anomalies of ocular globes | Cyclopia | synophthalmia | Congenital cystic eye | Congenital malformations of the eye [DA0B.5] Developmental or acquired deformities or conditions of gingiva Definition: This is a major developmental difference in the shape of a body part or organ compared to the average shape of that part. Also known as: Developmental or acquired deformities or conditions of gingiva | Gingival cleft | Furcation involvement | Inadequately attached gingiva | Minimally attached gingiva [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 [4A42.Z] Systemic sclerosis, unspecified Also known as: Systemic sclerosis, unspecified | Systemic sclerosis | Systemic scleroderma | progressive scleroderma | Acroscleriasis [KC20.Z] Conditions involving the umbilical cord, unspecified Also known as: Conditions involving the umbilical cord, unspecified | Conditions involving the umbilical cord [ED3Y] Cutaneous involvement in other specified neurological condition Also known as: Cutaneous involvement in other specified neurological condition | Spinal cord defect affecting the skin | Miscellaneous neurological conditions affecting the skin [2B33.5] Malignant lymphoma, not elsewhere classified Also known as: Malignant lymphoma, not elsewhere classified | Lymphoma NOS | NHL - [non-Hodgkin lymphoma] | non-Hodgkin lymphoma | Non-Hodgkin lymphoma, NOS [2A80.Z] Follicular lymphoma, unspecified Also known as: Follicular lymphoma, unspecified | Follicular lymphoma | Brill-Symmers' disease | large cell follicular non-Hodgkin lymphoma | diffuse follicle centre lymphoma [2B30.Z] Hodgkin lymphoma, unspecified Also known as: Hodgkin lymphoma, unspecified | Hodgkin lymphoma | Hodgkin disease | malignant lymphogranuloma | malignant lymphogranulomatosis === GRAPH WALKS === --- Walk 1 --- [9A20.00] Outward displacement of eyeball --PARENT--> [9A20.0] Axial displacement of eyeball --CHILD--> [9A20.00] Outward displacement of eyeball --- Walk 2 --- [9A20.00] Outward displacement of eyeball --PARENT--> [9A20.0] Axial displacement of eyeball --CHILD--> [9A20.01] Inward displacement of eyeball --- Walk 3 --- [LA10.Y] Other specified structural developmental anomalies of ocular globes --PARENT--> [LA10] Structural developmental anomalies of ocular globes Def: Any condition caused by failure of the ocular globes to correctly develop during the antenatal period.... --EXCLUDES--> [?] Holoprosencephaly with cyclopia or synophthalmia --- Walk 4 --- [LA10.Y] Other specified structural developmental anomalies of ocular globes --PARENT--> [LA10] Structural developmental anomalies of ocular globes Def: Any condition caused by failure of the ocular globes to correctly develop during the antenatal period.... --EXCLUDES--> [?] Holoprosencephaly with cyclopia or synophthalmia --- Walk 5 --- [DA0B.5] Developmental or acquired deformities or conditions of gingiva Def: This is a major developmental difference in the shape of a body part or organ compared to the average shape of that part.... --PARENT--> [DA0B] Gingival diseases Def: Gingivitis is inflammation of the tissues of the gingiva (gum) without loss of connective tissue.... --CHILD--> [DA0B.1] Catarrhal gingivitis --- Walk 6 --- [DA0B.5] Developmental or acquired deformities or conditions of gingiva Def: This is a major developmental difference in the shape of a body part or organ compared to the average shape of that part.... --PARENT--> [DA0B] Gingival diseases Def: Gingivitis is inflammation of the tissues of the gingiva (gum) without loss of connective tissue.... --RELATED_TO--> [?] Periodontal pocket Def: A periodontal pocket is an unusually deep gap in the gingival sulcus....
[ "[9A20.00] Outward displacement of eyeball\n --PARENT--> [9A20.0] Axial displacement of eyeball\n --CHILD--> [9A20.00] Outward displacement of eyeball", "[9A20.00] Outward displacement of eyeball\n --PARENT--> [9A20.0] Axial displacement of eyeball\n --CHILD--> [9A20.01] Inward displacement of eyeball", "[LA10.Y] Other specified structural developmental anomalies of ocular globes\n --PARENT--> [LA10] Structural developmental anomalies of ocular globes\n Def: Any condition caused by failure of the ocular globes to correctly develop during the antenatal period....\n --EXCLUDES--> [?] Holoprosencephaly with cyclopia or synophthalmia", "[LA10.Y] Other specified structural developmental anomalies of ocular globes\n --PARENT--> [LA10] Structural developmental anomalies of ocular globes\n Def: Any condition caused by failure of the ocular globes to correctly develop during the antenatal period....\n --EXCLUDES--> [?] Holoprosencephaly with cyclopia or synophthalmia", "[DA0B.5] Developmental or acquired deformities or conditions of gingiva\n Def: This is a major developmental difference in the shape of a body part or organ compared to the average shape of that part....\n --PARENT--> [DA0B] Gingival diseases\n Def: Gingivitis is inflammation of the tissues of the gingiva (gum) without loss of connective tissue....\n --CHILD--> [DA0B.1] Catarrhal gingivitis", "[DA0B.5] Developmental or acquired deformities or conditions of gingiva\n Def: This is a major developmental difference in the shape of a body part or organ compared to the average shape of that part....\n --PARENT--> [DA0B] Gingival diseases\n Def: Gingivitis is inflammation of the tissues of the gingiva (gum) without loss of connective tissue....\n --RELATED_TO--> [?] Periodontal pocket\n Def: A periodontal pocket is an unusually deep gap in the gingival sulcus...." ]
9A20.00
Outward displacement of eyeball
[ { "from_icd11": "9A20.00", "icd10_code": "H0520", "icd10_title": "Unspecified exophthalmos" }, { "from_icd11": "9A20.00", "icd10_code": "H05231", "icd10_title": "Hemorrhage of right orbit" }, { "from_icd11": "9A20.00", "icd10_code": "H05221", "icd10_title": "Edema of right orbit" }, { "from_icd11": "9A20.00", "icd10_code": "H05233", "icd10_title": "Hemorrhage of bilateral orbit" }, { "from_icd11": "9A20.00", "icd10_code": "H05222", "icd10_title": "Edema of left orbit" }, { "from_icd11": "9A20.00", "icd10_code": "H05223", "icd10_title": "Edema of bilateral orbit" }, { "from_icd11": "9A20.00", "icd10_code": "H05232", "icd10_title": "Hemorrhage of left orbit" }, { "from_icd11": "9A20.00", "icd10_code": "H05229", "icd10_title": "Edema of unspecified orbit" }, { "from_icd11": "9A20.00", "icd10_code": "H05239", "icd10_title": "Hemorrhage of unspecified orbit" }, { "from_icd11": "9A20.00", "icd10_code": "H05249", "icd10_title": "Constant exophthalmos, unspecified eye" }, { "from_icd11": "9A20.00", "icd10_code": "H052", "icd10_title": "Exophthalmic conditions" }, { "from_icd11": "4A42.Z", "icd10_code": "M3481", "icd10_title": "Systemic sclerosis with lung involvement" }, { "from_icd11": "4A42.Z", "icd10_code": "M3489", "icd10_title": "Other systemic sclerosis" }, { "from_icd11": "4A42.Z", "icd10_code": "M3483", "icd10_title": "Systemic sclerosis with polyneuropathy" }, { "from_icd11": "4A42.Z", "icd10_code": "M349", "icd10_title": "Systemic sclerosis, unspecified" } ]
H0520
Unspecified exophthalmos
A minimally invasive atypical lung resection is presented in Figure 2 . In the operation room, patients were placed as needed for the surgical procedure. Resection was performed in single lung ventilation anesthesia. However, the single lung ventilation was started only after removal of the dressing so that the retraction of the lung would not cause coil wire dislocation due to the fixation on the skin. A three-trocar technique was used for resection. After intrathoracic identification of the wire and the entrance point into the lung parenchyma, the lung tissue was elevated by grasping either the wire or the parenchyma around its point of entrance. The elevated portion of the lung was then resected in an atypical fashion using an endo-stapler device. The wire was cut intrathoracically and the resected specimen was introduced into a retrieval bag together with the rest of the coil wire. The specimen together with the bag was retrieved through an enlarged opening of the trocar site. After ending the single lung ventilation, the complete recruitment of lung areas as well as the tightness of the resection lines were ensured via direct visualization during final thoracoscopy as well as via the waterlock technique. Thoracic drains were placed if an extensive pleural adhesiolysis had been necessary or in case of several resections on the same site. Mechanical ventilation was ended directly after surgery.
3.982422
0.443848
sec[1]/sec[0]/p[3]
en
0.999996
PMC10047192
https://doi.org/10.3390/children10030542
[ "lung", "wire", "resection", "ventilation", "single", "atypical", "coil", "trocar", "technique", "entrance" ]
[ { "code": "CB40.Y", "title": "Other specified diseases of the respiratory system" }, { "code": "LA75.1", "title": "Agenesis of lung" }, { "code": "CA40.Z", "title": "Pneumonia, organism unspecified" }, { "code": "CB41", "title": "Respiratory failure" }, { "code": "NB32.3Y", "title": "Other injury of lung" }, { "code": "QB84", "title": "Follow-up care involving removal of fracture plate or other internal fixation device" }, { "code": "9B71.1&XS5S", "title": "Hypertensive Retinopathy, Stage 2, focal arteriolar narrowing, marked generalised arteriolar narrowing, arteriovenous nicking, opacity, “copper wiring” of arteriolar wall, or a combination of these signs" }, { "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" } ]
=== ICD-11 CODES FOUND === [CB40.Y] Other specified diseases of the respiratory system Also known as: Other specified diseases of the respiratory system | Secondary respiratory disorders | Respiratory disorders in diseases classified elsewhere | Diseases of bronchus, not elsewhere classified | Acquired bronchial diverticulum [LA75.1] Agenesis of lung Definition: This refers to the absence or rudimentary residua of an undeveloped lung. Also known as: Agenesis of lung | Pulmonary agenesis | absence of lung | aplasia of lung | apulmonism [CA40.Z] Pneumonia, organism unspecified Also known as: Pneumonia, organism unspecified | Pneumonia | infectious pneumonia | PN - [pneumonia] | lobar pneumonia NOS [CB41] Respiratory failure Definition: Respiratory failure is a life-threatening impairment of oxygenation or carbon dioxide (CO2) elimination. Respiratory failure may occur because of impaired gas exchange, decreased ventilation, or both. The level of oxygen in the blood becomes dangerously low or the level of carbon dioxide becomes dangerously high. Also known as: Respiratory failure | lung failure NOS | pulmonary failure Excludes: Acute respiratory distress syndrome | Respiratory arrest | Respiratory distress of newborn [NB32.3Y] Other injury of lung Also known as: Other injury of lung | Haematoma of lung | Traumatic hydropneumothorax | Acute traumatic lung congestion | Rupture of lung [QB84] Follow-up care involving removal of fracture plate or other internal fixation device Also known as: Follow-up care involving removal of fracture plate or other internal fixation device | Change of internal fixation device | change of fixation device | change of Kirschner wire | Checking of internal fixation device Excludes: removal of external fixation device [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 === GRAPH WALKS === --- Walk 1 --- [CB40.Y] Other specified diseases of the respiratory system --PARENT--> [CB40] Certain diseases of the respiratory system --RELATED_TO--> [?] Pulmonary sporotrichosis Def: Pulmonary forms of infection, although uncommon, can occur when Sporothrix schenckii conidia are inhaled. Symptoms of pulmonary sporotrichosis mimic those of tuberculosis including constitutional com... --- Walk 2 --- [CB40.Y] Other specified diseases of the respiratory system --PARENT--> [CB40] Certain diseases of the respiratory system --RELATED_TO--> [?] Alpha-1-antitrypsin deficiency Def: Alpha-1-antitrypsin deficiency (AATD) is a genetic disorder that manifests as pulmonary emphysema, liver cirrhosis and, rarely, as the skin disease panniculitis, and is characterised by low serum leve... --- Walk 3 --- [LA75.1] Agenesis of lung Def: This refers to the absence or rudimentary residua of an undeveloped lung.... --PARENT--> [LA75] Structural developmental anomalies of lungs Def: Any condition caused by failure of the lungs to correctly develop during the antenatal period.... --CHILD--> [LA75.1] Agenesis of lung Def: This refers to the absence or rudimentary residua of an undeveloped lung.... --- Walk 4 --- [LA75.1] Agenesis of lung Def: This refers to the absence or rudimentary residua of an undeveloped lung.... --PARENT--> [LA75] Structural developmental anomalies of lungs Def: Any condition caused by failure of the lungs to correctly develop during the antenatal period.... --CHILD--> [LA75.1] Agenesis of lung Def: This refers to the absence or rudimentary residua of an undeveloped lung.... --- Walk 5 --- [CA40.Z] Pneumonia, organism unspecified --PARENT--> [CA40] Pneumonia Def: A disease of the lungs, frequently but not always caused by an infection with bacteria, virus, fungus, or parasite. This disease is characterised by fever, chills, cough with sputum production, chest ... --PARENT--> [?] Lung infections Def: Any condition of the lungs, caused by an infection with a bacterial, viral, fungal, or parasitic source.... --- Walk 6 --- [CA40.Z] Pneumonia, organism unspecified --PARENT--> [CA40] Pneumonia Def: A disease of the lungs, frequently but not always caused by an infection with bacteria, virus, fungus, or parasite. This disease is characterised by fever, chills, cough with sputum production, chest ... --EXCLUDES--> [?] Pneumonitis Def: Pneumonitis is a general term that refers to inflammation of lung tissue. Pneumonitis includes the non-infectious lung diseases that cause inflammation of the interstitium of the lung tissue mainly....
[ "[CB40.Y] Other specified diseases of the respiratory system\n --PARENT--> [CB40] Certain diseases of the respiratory system\n --RELATED_TO--> [?] Pulmonary sporotrichosis\n Def: Pulmonary forms of infection, although uncommon, can occur when Sporothrix schenckii conidia are inhaled. \nSymptoms of pulmonary sporotrichosis mimic those of tuberculosis including constitutional com...", "[CB40.Y] Other specified diseases of the respiratory system\n --PARENT--> [CB40] Certain diseases of the respiratory system\n --RELATED_TO--> [?] Alpha-1-antitrypsin deficiency\n Def: Alpha-1-antitrypsin deficiency (AATD) is a genetic disorder that manifests as pulmonary emphysema, liver cirrhosis and, rarely, as the skin disease panniculitis, and is characterised by low serum leve...", "[LA75.1] Agenesis of lung\n Def: This refers to the absence or rudimentary residua of an undeveloped lung....\n --PARENT--> [LA75] Structural developmental anomalies of lungs\n Def: Any condition caused by failure of the lungs to correctly develop during the antenatal period....\n --CHILD--> [LA75.1] Agenesis of lung\n Def: This refers to the absence or rudimentary residua of an undeveloped lung....", "[LA75.1] Agenesis of lung\n Def: This refers to the absence or rudimentary residua of an undeveloped lung....\n --PARENT--> [LA75] Structural developmental anomalies of lungs\n Def: Any condition caused by failure of the lungs to correctly develop during the antenatal period....\n --CHILD--> [LA75.1] Agenesis of lung\n Def: This refers to the absence or rudimentary residua of an undeveloped lung....", "[CA40.Z] Pneumonia, organism unspecified\n --PARENT--> [CA40] Pneumonia\n Def: A disease of the lungs, frequently but not always caused by an infection with bacteria, virus, fungus, or parasite. This disease is characterised by fever, chills, cough with sputum production, chest ...\n --PARENT--> [?] Lung infections\n Def: Any condition of the lungs, caused by an infection with a bacterial, viral, fungal, or parasitic source....", "[CA40.Z] Pneumonia, organism unspecified\n --PARENT--> [CA40] Pneumonia\n Def: A disease of the lungs, frequently but not always caused by an infection with bacteria, virus, fungus, or parasite. This disease is characterised by fever, chills, cough with sputum production, chest ...\n --EXCLUDES--> [?] Pneumonitis\n Def: Pneumonitis is a general term that refers to inflammation of lung tissue. Pneumonitis includes the non-infectious lung diseases that cause inflammation of the interstitium of the lung tissue mainly...." ]
CB40.Y
Other specified diseases of the respiratory system
[ { "from_icd11": "LA75.1", "icd10_code": "Q333", "icd10_title": "Agenesis of lung" }, { "from_icd11": "CA40.Z", "icd10_code": "J189", "icd10_title": "Pneumonia, unspecified organism" }, { "from_icd11": "CA40.Z", "icd10_code": "J181", "icd10_title": "Lobar pneumonia, unspecified organism" }, { "from_icd11": "CA40.Z", "icd10_code": "J188", "icd10_title": "Other pneumonia, unspecified organism" }, { "from_icd11": "CA40.Z", "icd10_code": "J168", "icd10_title": "Pneumonia due to other specified infectious organisms" }, { "from_icd11": "CA40.Z", "icd10_code": "J180", "icd10_title": "Bronchopneumonia, unspecified organism" }, { "from_icd11": "CA40.Z", "icd10_code": "J17", "icd10_title": "Pneumonia in diseases classified elsewhere" }, { "from_icd11": "CA40.Z", "icd10_code": "J182", "icd10_title": "Hypostatic pneumonia, unspecified organism" }, { "from_icd11": "CA40.Z", "icd10_code": "J16", "icd10_title": "Pneumonia due to other infectious organisms, not elsewhere classified" }, { "from_icd11": "CA40.Z", "icd10_code": "J171", "icd10_title": "" }, { "from_icd11": "CA40.Z", "icd10_code": "J173", "icd10_title": "" }, { "from_icd11": "CA40.Z", "icd10_code": "J178", "icd10_title": "" }, { "from_icd11": "CA40.Z", "icd10_code": "J18", "icd10_title": "Pneumonia, unspecified organism" }, { "from_icd11": "CB41", "icd10_code": "J9622", "icd10_title": "Acute and chronic respiratory failure with hypercapnia" }, { "from_icd11": "CB41", "icd10_code": "J9620", "icd10_title": "Acute and chronic respiratory failure, unspecified whether with hypoxia or hypercapnia" } ]
Q333
Agenesis of lung
The patient initially presented with severe, likely acute, anemia at his consultation for radiation therapy for an early-stage NSCLC. His hemoglobin was found to be 4 g/dl, requiring urgent transfusion. Further workup of his anemia ruled out hemolysis, as he had a mildly elevated LDH and haptoglobin in the presence of a normal total bilirubin and ALT with no teardrop-shaped red blood cells on peripheral blood smear. Although teardrop forms are typically identified on bone marrow fibrosis, we suspect the lack of dacrocytes seen here likely relates to the acute nature of the patient’s clinical presentation. This would be analogous to acute panmyelosis with myelofibrosis, a rapidly progressive disease, which shows severe marrow fibrosis without circulating teardrop cells. Since the lifespan of a red blood cell is 120 days and this patient’s symptoms occurred much more quickly, we suspect that our assessment of the blood smear was prior to the development of dacrocytes. Severe anemia, as seen with our patient’s hemoglobin of 4 g/dl, from chronic myelofibrosis is usually accompanied by other blood abnormalities and splenomegaly. Splenomegaly was not seen. However, cases of acute myelofibrosis and autoimmune myelofibrosis are often not accompanied by splenomegaly, and autoimmune myelofibrosis, in particular, may not be associated with pancytopenia. In this case, the red cell line was primarily affected.
4.226563
0.895996
sec[2]/p[0]
en
0.999996
PMC8907522
https://doi.org/10.3389/fonc.2022.842620
[ "blood", "myelofibrosis", "anemia", "teardrop", "this", "splenomegaly", "likely", "hemoglobin", "cells", "smear" ]
[ { "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": "2A20.2", "title": "Primary myelofibrosis" }, { "code": "2A60.38", "title": "Acute panmyelosis with myelofibrosis" }, { "code": "2A2Z", "title": "Myeloproliferative neoplasm, unspecified" }, { "code": "3A9Z", "title": "Anaemias or other erythrocyte disorders, unspecified" }, { "code": "KA8Y", "title": "Other specified haemorrhagic or haematological disorders of fetus or newborn" } ]
=== 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 [2A20.2] Primary myelofibrosis Also known as: Primary myelofibrosis | myelofibrosis NOS | chronic idiopathic myelofibrosis | Myelofibrosis with myeloid metaplasia | idiopathic myelofibrosis with myeloid metaplasia Includes: chronic idiopathic myelofibrosis Excludes: Acute panmyelosis with myelofibrosis [2A60.38] Acute panmyelosis with myelofibrosis Definition: An acute myeloid leukaemia characterised by bone marrow fibrosis without preexisting primary myelofibrosis. Also known as: Acute panmyelosis with myelofibrosis | Acute myelofibrosis | acute panmyelosis | acute myelofibrosis without mention of remission | acute panmyelosis with myelofibrosis without mention of remission Includes: Acute myelofibrosis Excludes: Cases that meet criteria for AML with myelodysplasia related changes [2A2Z] Myeloproliferative neoplasm, unspecified Also known as: Myeloproliferative neoplasm, unspecified | MPN - [myeloproliferative neoplasms] | myelosclerosis | myeloid neoplasm | Myeloproliferative anaemia [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 === GRAPH WALKS === --- Walk 1 --- [3C0Z] Diseases of the blood or blood-forming organs, unspecified --PARENT--> [03] Diseases of the blood or blood-forming organs Def: This chapter includes diseases of the blood as well as diseases of blood forming organs.... --EXCLUDES--> [?] Pregnancy, childbirth or the puerperium Def: A group of conditions characterised as occurring during the period of time from conception to delivery (pregnancy), during labour and delivery (childbirth) or during the approximately six weeks after ... --- Walk 2 --- [3C0Z] Diseases of the blood or blood-forming organs, unspecified --PARENT--> [03] Diseases of the blood or blood-forming organs Def: This chapter includes diseases of the blood as well as diseases of blood forming organs.... --CHILD--> [?] Coagulation defects, purpura or other haemorrhagic or related conditions Def: A condition caused by determinants arising during the antenatal period, after birth or by genetically inherited factors, leading to coagulation defects. This condition is characterised by increased br... --- Walk 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--> [MF50.40] Macroscopic haematuria --- Walk 4 --- [MF50.4Z] Haematuria, unspecified --PARENT--> [MF50.4] Haematuria Def: Hematuria means presence of blood or red blood cells (RBCs) in the urine. There are two types of hematuria: gross hematuria (when one can see the blood in the urine) and microscopic hematuria (when th... --CHILD--> [MF50.41] Microscopic 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--> [MA12.1] Finding of cocaine in blood --- Walk 6 --- [MA12.1] Finding of cocaine in blood --PARENT--> [MA12] Clinical findings of drugs, medicaments and biological substances in blood, blood-forming organs, or the immune system --CHILD--> [MA12.0] Finding of opiate drug in blood
[ "[3C0Z] Diseases of the blood or blood-forming organs, unspecified\n --PARENT--> [03] Diseases of the blood or blood-forming organs\n Def: This chapter includes diseases of the blood as well as diseases of blood forming organs....\n --EXCLUDES--> [?] Pregnancy, childbirth or the puerperium\n Def: A group of conditions characterised as occurring during the period of time from conception to delivery (pregnancy), during labour and delivery (childbirth) or during the approximately six weeks after ...", "[3C0Z] Diseases of the blood or blood-forming organs, unspecified\n --PARENT--> [03] Diseases of the blood or blood-forming organs\n Def: This chapter includes diseases of the blood as well as diseases of blood forming organs....\n --CHILD--> [?] Coagulation defects, purpura or other haemorrhagic or related conditions\n Def: A condition caused by determinants arising during the antenatal period, after birth or by genetically inherited factors, leading to coagulation defects. This condition is characterised by increased br...", "[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", "[MF50.4Z] Haematuria, unspecified\n --PARENT--> [MF50.4] Haematuria\n Def: Hematuria means presence of blood or red blood cells (RBCs) in the urine. There are two types of hematuria: gross hematuria (when one can see the blood in the urine) and microscopic hematuria (when th...\n --CHILD--> [MF50.41] Microscopic haematuria", "[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--> [MA12.1] Finding of cocaine in blood", "[MA12.1] Finding of cocaine in blood\n --PARENT--> [MA12] Clinical findings of drugs, medicaments and biological substances in blood, blood-forming organs, or the immune system\n --CHILD--> [MA12.0] Finding of opiate drug in blood" ]
3C0Z
Diseases of the blood or blood-forming organs, unspecified
[ { "from_icd11": "3C0Z", "icd10_code": "D75A", "icd10_title": "Glucose-6-phosphate dehydrogenase (G6PD) deficiency without anemia" }, { "from_icd11": "3C0Z", "icd10_code": "D7581", "icd10_title": "Myelofibrosis" }, { "from_icd11": "3C0Z", "icd10_code": "D7582", "icd10_title": "Heparin induced thrombocytopenia (HIT)" }, { "from_icd11": "3C0Z", "icd10_code": "D7589", "icd10_title": "Other specified diseases of blood and blood-forming organs" }, { "from_icd11": "3C0Z", "icd10_code": "D759", "icd10_title": "Disease of blood and blood-forming organs, unspecified" }, { "from_icd11": "3C0Z", "icd10_code": "D763", "icd10_title": "Other histiocytosis syndromes" }, { "from_icd11": "3C0Z", "icd10_code": "Q899", "icd10_title": "Congenital malformation, unspecified" }, { "from_icd11": "3C0Z", "icd10_code": "III", "icd10_title": "" }, { "from_icd11": "3C0Z", "icd10_code": "D70-D77", "icd10_title": "" }, { "from_icd11": "3C0Z", "icd10_code": "D75", "icd10_title": "Other and unspecified diseases of blood and blood-forming organs" }, { "from_icd11": "3C0Z", "icd10_code": "D77", "icd10_title": "Other disorders of blood and blood-forming organs in diseases classified elsewhere" }, { "from_icd11": "3C0Z", "icd10_code": "D758", "icd10_title": "Other specified diseases of blood and blood-forming organs" }, { "from_icd11": "3C0Z", "icd10_code": "D76", "icd10_title": "Other specified diseases with participation of lymphoreticular and reticulohistiocytic tissue" }, { "from_icd11": "MF50.4Z", "icd10_code": "R310", "icd10_title": "Gross hematuria" }, { "from_icd11": "MF50.4Z", "icd10_code": "R312", "icd10_title": "Other microscopic hematuria" } ]
D75A
Glucose-6-phosphate dehydrogenase (G6PD) deficiency without anemia
Due to the provisional diagnosis of fulminant myocarditis with cardiogenic shock, the patient was taken for cardiac catheterization and possible placement of mechanical heart support such as Impella or extracorporeal membrane oxygenation (ECMO) support. Before the procedure, just seven hours after admission, the patient had the first cardiac arrest with the primary rhythm of pulseless electrical activity (PEA). Advanced cardiac life support (ACLS) protocol was initiated and return of spontaneous circulation (ROSC) was achieved. Post ROSC she underwent a left ventriculogram (LVG), coronary angiogram, and right heart catheterization (RHC). LVG showed global hypokinesis with severely reduced ejection fraction of around 10%. The coronary arteries were noted to be patent. RHC findings were consistent with biventricular failure, with pulmonary capillary wedge pressure (PCWP) of 25 mmHg (normal range: 6-12 mmHg), Cardiac index or CI of 0.9 L/min/mm 3 (normal >2.4L/min/mm 3 ) and right atrial pressures of 23 mmHg (normal range: 2-6 mmHg). Femoral artery anatomy was found to be unsuitable for an Impella device insertion, and hence cardiothoracic surgery was contacted for placement on ECMO support. However, unfortunately, at this time, the patient had another cardiac arrest, again with a rhythm of pulseless electrical activity. At this time the patient could not be revived despite all resuscitative efforts.
3.972656
0.971191
sec[1]/p[4]
en
0.999996
PMC10200269
https://doi.org/10.7759/cureus.37942
[ "cardiac", "support", "mmhg", "catheterization", "placement", "heart", "impella", "ecmo", "arrest", "rhythm" ]
[ { "code": "BE2Y", "title": "Other specified diseases of the circulatory system" }, { "code": "BC4Z", "title": "Diseases of the myocardium or cardiac chambers, unspecified" }, { "code": "BD1Z", "title": "Heart failure, unspecified" }, { "code": "LA8Z", "title": "Structural developmental anomaly of heart or great vessels, unspecified" }, { "code": "BA41.Z", "title": "Acute myocardial infarction, unspecified" }, { "code": "QE70.0", "title": "Inadequate family support" }, { "code": "QE31.Z", "title": "Insufficient social welfare support, unspecified" }, { "code": "QE70.Z", "title": "Problems related to primary support group, including family circumstances, unspecified" }, { "code": "QE31.0", "title": "Insufficient social welfare support, child protection" }, { "code": "QE30.3", "title": "Insufficient social insurance support, family support" } ]
=== 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 [BC4Z] Diseases of the myocardium or cardiac chambers, unspecified Also known as: Diseases of the myocardium or cardiac chambers, unspecified | Heart disease NOS | cardiac disease NOS [BD1Z] Heart failure, unspecified Also known as: Heart failure, unspecified | myocardial failure | cardiac decompensation | cardiac failure | cardiac failure NOS [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 [BA41.Z] Acute myocardial infarction, unspecified Also known as: Acute myocardial infarction, unspecified | Acute myocardial infarction | cardiac attack | heart attack | acute cardiac infarction [QE70.0] Inadequate family support Also known as: Inadequate family support | inadequate family support NOS [QE31.Z] Insufficient social welfare support, unspecified Also known as: Insufficient social welfare support, unspecified | Insufficient social welfare support | insufficient welfare support | inadequate welfare support [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 [QE31.0] Insufficient social welfare support, child protection Also known as: Insufficient social welfare support, child protection | inadequate child protection support | insufficient child protection support [QE30.3] Insufficient social insurance support, family support Also known as: Insufficient social insurance support, family support | inadequate family insurance support | insufficient family insurance support === 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... --RELATED_TO--> [?] Cerebrovascular diseases Def: This is a group of brain dysfunctions related to disease of the blood vessels supplying the brain. This includes “stroke”, which includes the following entities: Intracerebral haemorrhage; Subarachnoi... --- 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... --EXCLUDES--> [?] Certain conditions originating in the perinatal period Def: This chapter includes conditions that have their origin in the perinatal period even though death or morbidity occurs later.... --- Walk 3 --- [BC4Z] Diseases of the myocardium or cardiac chambers, unspecified --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--> [BC40] Acquired atrial abnormality Def: A postnatal pathological change in form or function of one or both atriums.... --- Walk 4 --- [BC4Z] Diseases of the myocardium or cardiac chambers, unspecified --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--> [BC41] Acquired ventricular abnormality Def: A postnatal pathological change in form or function of a ventricle.... --- Walk 5 --- [BD1Z] Heart failure, unspecified --PARENT--> [?] Heart failure --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 6 --- [BD1Z] Heart failure, unspecified --PARENT--> [?] Heart failure --CHILD--> [BD11] Left ventricular failure Def: A clinical syndrome characterised by abnormalities of left ventricular function resulting in pulmonary congestion and fluid retention....
[ "[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 --RELATED_TO--> [?] Cerebrovascular diseases\n Def: This is a group of brain dysfunctions related to disease of the blood vessels supplying the brain. This includes “stroke”, which includes the following entities: Intracerebral haemorrhage; Subarachnoi...", "[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 --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....", "[BC4Z] Diseases of the myocardium or cardiac chambers, unspecified\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--> [BC40] Acquired atrial abnormality\n Def: A postnatal pathological change in form or function of one or both atriums....", "[BC4Z] Diseases of the myocardium or cardiac chambers, unspecified\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--> [BC41] Acquired ventricular abnormality\n Def: A postnatal pathological change in form or function of a ventricle....", "[BD1Z] Heart failure, unspecified\n --PARENT--> [?] Heart failure\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....", "[BD1Z] Heart failure, unspecified\n --PARENT--> [?] Heart failure\n --CHILD--> [BD11] Left ventricular failure\n Def: A clinical syndrome characterised by abnormalities of left ventricular function resulting in pulmonary congestion and fluid retention...." ]
BE2Y
Other specified diseases of the circulatory system
[ { "from_icd11": "BC4Z", "icd10_code": "I5181", "icd10_title": "Takotsubo syndrome" }, { "from_icd11": "BC4Z", "icd10_code": "I5189", "icd10_title": "Other ill-defined heart diseases" }, { "from_icd11": "BC4Z", "icd10_code": "I519", "icd10_title": "Heart disease, unspecified" }, { "from_icd11": "BC4Z", "icd10_code": "I510", "icd10_title": "Cardiac septal defect, acquired" }, { "from_icd11": "BC4Z", "icd10_code": "I515", "icd10_title": "Myocardial degeneration" }, { "from_icd11": "BC4Z", "icd10_code": "I51", "icd10_title": "Complications and ill-defined descriptions of heart disease" }, { "from_icd11": "BC4Z", "icd10_code": "I516", "icd10_title": "" }, { "from_icd11": "BC4Z", "icd10_code": "I518", "icd10_title": "Other ill-defined heart diseases" }, { "from_icd11": "BD1Z", "icd10_code": "I5023", "icd10_title": "Acute on chronic systolic (congestive) heart failure" }, { "from_icd11": "BD1Z", "icd10_code": "I5030", "icd10_title": "Unspecified diastolic (congestive) heart failure" }, { "from_icd11": "BD1Z", "icd10_code": "I5031", "icd10_title": "Acute diastolic (congestive) heart failure" }, { "from_icd11": "BD1Z", "icd10_code": "I5022", "icd10_title": "Chronic systolic (congestive) heart failure" }, { "from_icd11": "BD1Z", "icd10_code": "I5084", "icd10_title": "End stage heart failure" }, { "from_icd11": "BD1Z", "icd10_code": "I5020", "icd10_title": "Unspecified systolic (congestive) heart failure" }, { "from_icd11": "BD1Z", "icd10_code": "I5021", "icd10_title": "Acute systolic (congestive) heart failure" } ]
I5181
Takotsubo syndrome
Hypercoagulability in the setting of cancer is a common occurrence that results from a multitude of pathologic mechanisms that predispose cancer patients to the development of thrombosis . Venous thromboembolism is the most frequently observed type of thrombosis in cancer patients . Arterial thrombosis is much less prevalent than venous thrombosis in cancer patients, but arterial thrombosis, including aortic thrombosis, can also pose a life-threatening risk. Chemotherapeutic drugs, including platinum-based agents, vascular endothelial growth factor inhibitors, tyrosine kinase inhibitors, and taxanes, have been associated with higher rates of arterial thromboembolism . The management of arterial thrombosis of uncertain etiology often requires a review of the literature and often involves the input of hematologists . Here, we present a case of a 68-year-old male with a history of stage IIIA colon cancer who presented to the emergency department with symptoms of nausea, vomiting, abdominal pain, diarrhea, and fatigue and received a CT scan of the abdomen and pelvis, which incidentally revealed a mural thrombus in the aortic wall, extending from the renal arteries to the mid-abdominal aorta. This case report highlights the importance of awareness of potential arterial thrombotic complications in patients undergoing chemotherapy, especially with combination chemotherapy of capecitabine and oxaliplatin.
4.1875
0.923828
sec[0]/p[0]
en
0.999998
37323352
https://doi.org/10.7759/cureus.39042
[ "thrombosis", "cancer", "arterial", "patients", "that", "venous", "thromboembolism", "including", "aortic", "inhibitors" ]
[ { "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": "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" } ]
=== 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) [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 === 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--> [DD30.0] Acute mesenteric arterial infarction Def: Acute mesenteric arterial infarction is an ischemic disorder of sudden interruption of mesenteric arterial flow because of occlusion of mesenteric artery. This may be further subdivided into acute mes... --- Walk 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--> [?] 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 4 --- [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 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--> [DD30.0] Acute mesenteric arterial infarction\n Def: Acute mesenteric arterial infarction is an ischemic disorder of sudden interruption of mesenteric arterial flow because of occlusion of mesenteric artery. This may be further subdivided into acute mes...", "[DD30.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--> [?] Obstetric blood-clot embolism\n Def: A condition characterised by the lodging of a blood clot (a specific type of embolus known as a thrombus) in the bloodstream, which can cause a blockage associated with the physiological and other cha...", "[JA61.Y] Other specified venous complications in pregnancy\n --PARENT--> [JA61] Venous complications in pregnancy\n --EXCLUDES--> [?] Complications following abortion, ectopic or molar pregnancy\n Def: Any complication affecting pregnant females, caused by or subsequent to abortion, ectopic, and molar pregnancy....", "[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
Although the cause of the liver damage has not been clearly identified, both SjS and pregnancy could be the cause of acute liver injury. SjS is associated with various hepatic abnormalities, including transaminitis, primary biliary cholangitis, or autoimmune hepatitis. The patient excluded the possibility of hepatotoxic drugs, fatty liver disease, fatty liver disease, and chronic viral infections, but there is still a possibility of Sjogren’s syndrome inducing autoimmune liver disease . SjS induced primary biliary cirrhosis (PBC) or sclerosing cholangitis were also considered but eventually excluded after a meticulous evaluation. Hepatic fibrosis may be induced by SjS and lead to abnormal liver function , but due to the unavailability of liver biopsy during pregnancy to confirm the occurrence of fibrosis, SjS induced liver fibrosis is not the primary cause of consideration in this case. Given the fact that liver enzymes normalized after pregnancy termination, pregnancy itself was more likely to be the cause of hepatic injury, rather than Sjögren’s syndrome. As shown in the previous research, women with SjS were more likely to have premature birth . Our patient presented the initial symptoms of SjS-associated IPO at gestation of 29 weeks, and was successfully treated with combined immunosuppressive therapy by multidiscipline team resulting in an uneventful caesarean delivery at 33 weeks’ gestation.
4.105469
0.947754
sec[2]/p[4]
en
0.999994
37365520
https://doi.org/10.1186/s12884-023-05757-5
[ "liver", "cause", "pregnancy", "hepatic", "induced", "fibrosis", "injury", "associated", "biliary", "cholangitis" ]
[ { "code": "DB9Z", "title": "Diseases of liver, unspecified" }, { "code": "DB97.Z", "title": "Inflammatory liver disease, unspecified" }, { "code": "DB99.7", "title": "Hepatic failure without mention whether acute or chronic" }, { "code": "LB20.0Y", "title": "Other specified structural developmental anomalies of liver" }, { "code": "LB20.0Z", "title": "Structural developmental anomalies of liver, unspecified" }, { "code": "MG48", "title": "Unknown or unspecified causes of morbidity" }, { "code": "PB6Z", "title": "Unspecified unintentional cause of morbidity or mortality" }, { "code": "NF0Z", "title": "Unspecified effects of external causes" }, { "code": "JB06.Z", "title": "Obstructed labour due to unspecified causes" }, { "code": "NF0Y", "title": "Other specified effects of external causes" } ]
=== ICD-11 CODES FOUND === [DB9Z] Diseases of liver, unspecified Also known as: Diseases of liver, unspecified | liver disease | liver condition NOS | organ liver disease | hepatopathy [DB97.Z] Inflammatory liver disease, unspecified Also known as: Inflammatory liver disease, unspecified | Certain specified inflammatory liver diseases | Nonspecific reactive hepatitis | inflammatory liver disease | hepatitis NOS [DB99.7] Hepatic failure without mention whether acute or chronic Also known as: Hepatic failure without mention whether acute or chronic | liver decompensation | liver function failure | hepatic failure NOS | liver failure NOS [LB20.0Y] Other specified structural developmental anomalies of liver Also known as: Other specified structural developmental anomalies of liver | Alagille syndrome | Alagille-Watson syndrome | Arteriohepatic dysplasia | Syndromic bile duct paucity [LB20.0Z] Structural developmental anomalies of liver, unspecified Also known as: Structural developmental anomalies of liver, unspecified | Structural developmental anomalies of liver | Malformations of liver | congenital anomaly of liver | congenital malformation of liver [MG48] Unknown or unspecified causes of morbidity Also known as: Unknown or unspecified causes of morbidity | undetermined cause | unknown cause of disease | illness | Illness NOS Includes: Undiagnosed disease, not specified as to the site or system involved [PB6Z] Unspecified unintentional cause of morbidity or mortality Also known as: Unspecified unintentional cause of morbidity or mortality | Exposure to unspecified factor | Exposure to unspecified factor causing fracture | Exposure to unspecified factor causing other and unspecified injury | accidental cause NOS [NF0Z] Unspecified effects of external causes Also known as: Unspecified effects of external causes [JB06.Z] Obstructed labour due to unspecified causes Also known as: Obstructed labour due to unspecified causes | Obstructed labour due to other causes [NF0Y] Other specified effects of external causes Also known as: Other specified effects of external causes | Adverse effect physical factor | Jet lag | Environmental exposure, not elsewhere classified | exposure NOS === GRAPH WALKS === --- Walk 1 --- [DB9Z] Diseases of liver, unspecified --PARENT--> [?] Diseases of liver --PARENT--> [13] Diseases of the digestive system --- Walk 2 --- [DB9Z] Diseases of liver, unspecified --PARENT--> [?] Diseases of liver --EXCLUDES--> [?] Unspecified jaundice Def: A clinical manifestation of hyperbilirubinemia of unspecified origin, characterised by the yellowish staining of the skin; mucus membranes and sclera.... --- Walk 3 --- [DB97.Z] Inflammatory liver disease, unspecified --PARENT--> [DB97] Certain specified inflammatory liver diseases --RELATED_TO--> [?] Hepatic sarcoidosis Def: This is a syndrome involving abnormal collections of chronic inflammatory cells (granulomas) that can form as nodules in multiple organs, of the liver.... --- Walk 4 --- [DB97.Z] Inflammatory liver disease, unspecified --PARENT--> [DB97] Certain specified inflammatory liver diseases --EXCLUDES--> [?] Acute or subacute hepatic failure Def: Acute and subacute liver failure is characterised by onset of coagulopathy and/or hepatic encephalopathy within 8 weeks of onset of symptoms in a patient without previously known liver diseases.... --- Walk 5 --- [DB99.7] Hepatic failure without mention whether acute or chronic --PARENT--> [DB99] 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.... --EXCLUDES--> [?] Drug-induced or toxic liver disease Def: Drug-induced or toxic liver disease is hepatotoxicity as injury to the liver that is associated with impaired liver function caused by exposure to a drug or another noninfectious agent.... --- Walk 6 --- [DB99.7] Hepatic failure without mention whether acute or chronic --PARENT--> [DB99] 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.... --CHILD--> [DB99.2] Hepatorenal syndrome
[ "[DB9Z] Diseases of liver, unspecified\n --PARENT--> [?] Diseases of liver\n --PARENT--> [13] Diseases of the digestive system", "[DB9Z] Diseases of liver, unspecified\n --PARENT--> [?] Diseases of liver\n --EXCLUDES--> [?] Unspecified jaundice\n Def: A clinical manifestation of hyperbilirubinemia of unspecified origin, characterised by the yellowish staining of the skin; mucus membranes and sclera....", "[DB97.Z] Inflammatory liver disease, unspecified\n --PARENT--> [DB97] Certain specified inflammatory liver diseases\n --RELATED_TO--> [?] Hepatic sarcoidosis\n Def: This is a syndrome involving abnormal collections of chronic inflammatory cells (granulomas) that can form as nodules in multiple organs, of the liver....", "[DB97.Z] Inflammatory liver disease, unspecified\n --PARENT--> [DB97] Certain specified inflammatory liver diseases\n --EXCLUDES--> [?] Acute or subacute hepatic failure\n Def: Acute and subacute liver failure is characterised by onset of coagulopathy and/or hepatic encephalopathy within 8 weeks of onset of symptoms in a patient without previously known liver diseases....", "[DB99.7] Hepatic failure without mention whether acute or chronic\n --PARENT--> [DB99] 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....\n --EXCLUDES--> [?] Drug-induced or toxic liver disease\n Def: Drug-induced or toxic liver disease is hepatotoxicity as injury to the liver that is associated with impaired liver function caused by exposure to a drug or another noninfectious agent....", "[DB99.7] Hepatic failure without mention whether acute or chronic\n --PARENT--> [DB99] 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....\n --CHILD--> [DB99.2] Hepatorenal syndrome" ]
DB9Z
Diseases of liver, unspecified
[ { "from_icd11": "DB9Z", "icd10_code": "K7681", "icd10_title": "Hepatopulmonary syndrome" }, { "from_icd11": "DB9Z", "icd10_code": "K7689", "icd10_title": "Other specified diseases of liver" }, { "from_icd11": "DB9Z", "icd10_code": "K769", "icd10_title": "Liver disease, unspecified" }, { "from_icd11": "DB9Z", "icd10_code": "K77", "icd10_title": "Liver disorders in diseases classified elsewhere" }, { "from_icd11": "DB9Z", "icd10_code": "K762", "icd10_title": "Central hemorrhagic necrosis of liver" }, { "from_icd11": "DB9Z", "icd10_code": "K70-K77", "icd10_title": "" }, { "from_icd11": "DB9Z", "icd10_code": "K778", "icd10_title": "" }, { "from_icd11": "DB9Z", "icd10_code": "K72", "icd10_title": "Hepatic failure, not elsewhere classified" }, { "from_icd11": "DB9Z", "icd10_code": "K76", "icd10_title": "Other diseases of liver" }, { "from_icd11": "DB9Z", "icd10_code": "K768", "icd10_title": "Other specified diseases of liver" }, { "from_icd11": "DB97.Z", "icd10_code": "K7581", "icd10_title": "Nonalcoholic steatohepatitis (NASH)" }, { "from_icd11": "DB97.Z", "icd10_code": "K7589", "icd10_title": "Other specified inflammatory liver diseases" }, { "from_icd11": "DB97.Z", "icd10_code": "K759", "icd10_title": "Inflammatory liver disease, unspecified" }, { "from_icd11": "DB97.Z", "icd10_code": "K752", "icd10_title": "Nonspecific reactive hepatitis" }, { "from_icd11": "DB97.Z", "icd10_code": "K75", "icd10_title": "Other inflammatory liver diseases" } ]
K7681
Hepatopulmonary syndrome
A 36-year-old male semi-professional runner was referred for examination after collapsing at the finish of a half-marathon run. He had a 15-year-long history of long-distance running without symptoms. His ECG revealed signs of left ventricular hypertrophy (LVH) with left atrial enlargement and T-wave inversions in leads II, III, aVF, V3–V6 with an ST-segment depression of 1 mm in leads II, III, and aVF . Transthoracic echocardiography revealed asymmetric hypertrophy of the interventricular septum of 17 mm suggestive of hypertrophic cardiomyopathy (HCM). The patient had no family history of HCM. CMR confirmed the diagnosis, showing also a mild left ventricular outflow tract obstruction (LVOTO) with systolic anterior movement (SAM) of the anterior mitral valve leaflet. There were no signs of non-ischemic LGE but there was a small subendocardial scar in the hypertrophied interventricular septum , typical for prior small myocardial infarction. The patient had no signs of coronary artery disease on the CTCA. Other possible causes of secondary cardiac hypertrophy have been excluded, as per the guidelines on the diagnosis and treatment of hypertrophic cardiomyopathy . Therefore, the MI was most probably attributable to a mismatch between oxygen demand and supply during intensive exercise. The patient was advised to refrain from competitive, strenuous exercises and was put on a small dose of beta-blocker.
4.082031
0.976074
sec[1]/sec[1]/p[0]
en
0.999998
PMC10417275
https://doi.org/10.3390/diagnostics13152473
[ "hypertrophy", "small", "long", "ventricular", "leads", "interventricular", "septum", "hypertrophic", "cardiomyopathy", "semi" ]
[ { "code": "FB32.Y", "title": "Other specified disorders of muscles" }, { "code": "FB86.11", "title": "Hypertrophy of bone" }, { "code": "MA01.Z", "title": "Enlarged lymph nodes, unspecified" }, { "code": "FB4Y", "title": "Other specified disorders of synovium or tendon" }, { "code": "FA34.1", "title": "Disorder of ligament" }, { "code": "MF54.2", "title": "Small kidney" }, { "code": "DA9Z", "title": "Diseases of small intestine, unspecified" }, { "code": "GA16.Y", "title": "Other specified acquired abnormalities of uterus, except cervix" }, { "code": "KA20.0Z", "title": "Small for gestational age, unspecified" }, { "code": "1A40.Z", "title": "Infectious gastroenteritis or colitis without specification of infectious agent" } ]
=== ICD-11 CODES FOUND === [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 [FB86.11] Hypertrophy of bone Also known as: Hypertrophy of bone | bone thickening | periosteum thickening | Infantile cortical hyperostoses | Post traumatic subperiosteal ossification [MA01.Z] Enlarged lymph nodes, unspecified Also known as: Enlarged lymph nodes, unspecified | Enlarged lymph nodes | swollen glands | Lymphadenopathy | adenopathy [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 [FA34.1] Disorder of ligament Also known as: Disorder of ligament | disorder of ligament, unspecified site | ligament disorder | disease of ligament | ligament deformity Excludes: Chronic instability of knee | familial ligamentous laxity [MF54.2] Small kidney Definition: A condition characterised by a kidney smaller in size and weight than the average (less than 11 centimetres long, 5-7.5 centimetres wide, 2.5 centimetres thick, and weighing less than 120 grams). Also known as: Small kidney | Small kidney, unilateral | unilateral small kidney | Small kidney, bilateral [DA9Z] Diseases of small intestine, unspecified Also known as: Diseases of small intestine, unspecified [GA16.Y] Other specified acquired abnormalities of uterus, except cervix Also known as: Other specified acquired abnormalities of uterus, except cervix | Polyp of corpus uteri | intrauterine polyp | polyp of body of uterus | polyp of uterus [KA20.0Z] Small for gestational age, unspecified Also known as: Small for gestational age, unspecified | Small for gestational age | Small-for-dates | small fetus or newborn for gestational age | dysmaturity [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 --- [FB32.Y] Other specified disorders of muscles --PARENT--> [FB32] Certain specified disorders of muscle Def: This is an impairment of health or a condition of abnormal functioning of the muscle that does not fit in another category.... --EXCLUDES--> [?] Cramp or spasm --- Walk 2 --- [FB32.Y] Other specified disorders of muscles --PARENT--> [FB32] Certain specified disorders of muscle Def: This is an impairment of health or a condition of abnormal functioning of the muscle that does not fit in another category.... --EXCLUDES--> [?] Myalgia Def: This is a disorder characterised by pain in a muscle or group of muscles.... --- Walk 3 --- [FB86.11] Hypertrophy of bone --PARENT--> [FB86.1] Bone hyperplasias --CHILD--> [FB86.11] Hypertrophy of bone --- Walk 4 --- [FB86.11] Hypertrophy of bone --PARENT--> [FB86.1] Bone hyperplasias --CHILD--> [FB86.10] Hypertrophic osteoarthropathy Def: Hypertrophic osteoarthropathy (HOA) is a syndrome of clubbing of the digits, subperiosteal new bone formation (periostitis) affecting the long bones, and arthritis. The primary hereditary form is asso... --- Walk 5 --- [MA01.Z] Enlarged lymph nodes, unspecified --PARENT--> [MA01] Enlarged lymph nodes Def: Enlarged lymph node is called lymphadenopathy which means the abnormal enlargement of lymph nodes.... --EXCLUDES--> [?] Nonspecific mesenteric lymphadenitis --- Walk 6 --- [MA01.Z] Enlarged lymph nodes, unspecified --PARENT--> [MA01] Enlarged lymph nodes Def: Enlarged lymph node is called lymphadenopathy which means the abnormal enlargement of lymph nodes.... --CHILD--> [MA01.1] Generalised lymph node enlargement
[ "[FB32.Y] Other specified disorders of muscles\n --PARENT--> [FB32] Certain specified disorders of muscle\n Def: This is an impairment of health or a condition of abnormal functioning of the muscle that does not fit in another category....\n --EXCLUDES--> [?] Cramp or spasm", "[FB32.Y] Other specified disorders of muscles\n --PARENT--> [FB32] Certain specified disorders of muscle\n Def: This is an impairment of health or a condition of abnormal functioning of the muscle that does not fit in another category....\n --EXCLUDES--> [?] Myalgia\n Def: This is a disorder characterised by pain in a muscle or group of muscles....", "[FB86.11] Hypertrophy of bone\n --PARENT--> [FB86.1] Bone hyperplasias\n --CHILD--> [FB86.11] Hypertrophy of bone", "[FB86.11] Hypertrophy of bone\n --PARENT--> [FB86.1] Bone hyperplasias\n --CHILD--> [FB86.10] Hypertrophic osteoarthropathy\n Def: Hypertrophic osteoarthropathy (HOA) is a syndrome of clubbing of the digits, subperiosteal new bone formation (periostitis) affecting the long bones, and arthritis. The primary hereditary form is asso...", "[MA01.Z] Enlarged lymph nodes, unspecified\n --PARENT--> [MA01] Enlarged lymph nodes\n Def: Enlarged lymph node is called lymphadenopathy which means the abnormal enlargement of lymph nodes....\n --EXCLUDES--> [?] Nonspecific mesenteric lymphadenitis", "[MA01.Z] Enlarged lymph nodes, unspecified\n --PARENT--> [MA01] Enlarged lymph nodes\n Def: Enlarged lymph node is called lymphadenopathy which means the abnormal enlargement of lymph nodes....\n --CHILD--> [MA01.1] Generalised lymph node enlargement" ]
FB32.Y
Other specified disorders of muscles
[ { "from_icd11": "FB32.Y", "icd10_code": "M6281", "icd10_title": "Muscle weakness (generalized)" }, { "from_icd11": "FB86.11", "icd10_code": "M89351", "icd10_title": "Hypertrophy of bone, right femur" }, { "from_icd11": "FB86.11", "icd10_code": "M89361", "icd10_title": "Hypertrophy of bone, right tibia" }, { "from_icd11": "FB86.11", "icd10_code": "M8938", "icd10_title": "Hypertrophy of bone, other site" }, { "from_icd11": "FB86.11", "icd10_code": "M89371", "icd10_title": "Hypertrophy of bone, right ankle and foot" }, { "from_icd11": "FB86.11", "icd10_code": "M89363", "icd10_title": "Hypertrophy of bone, right fibula" }, { "from_icd11": "FB86.11", "icd10_code": "M89333", "icd10_title": "Hypertrophy of bone, right radius" }, { "from_icd11": "FB86.11", "icd10_code": "M89362", "icd10_title": "Hypertrophy of bone, left tibia" }, { "from_icd11": "FB86.11", "icd10_code": "M8930", "icd10_title": "Hypertrophy of bone, unspecified site" }, { "from_icd11": "FB86.11", "icd10_code": "M893", "icd10_title": "Hypertrophy of bone" }, { "from_icd11": "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": "FA34.1", "icd10_code": "M2420", "icd10_title": "Disorder of ligament, unspecified site" }, { "from_icd11": "FA34.1", "icd10_code": "M2428", "icd10_title": "Disorder of ligament, vertebrae" }, { "from_icd11": "FA34.1", "icd10_code": "M24272", "icd10_title": "Disorder of ligament, left ankle" } ]
M6281
Muscle weakness (generalized)
A man in his late 70s noticed shortness of breath on exertion 5 months prior. He presented to a previous physician, and computed tomography (CT) revealed moderate emphysema, a nodule in the right lower lobe of the lung, and a mass in the upper lateral part of the right breast. PET showed accumulation of 18 F-FDG in a nodule in the right lower lobe of the lung and a mass in the right breast with a maximum standardized uptake value of 4.23 and 3.11, respectively . The nodule in the right lower lobe was diagnosed as T1bN0M0, Stage IA2 lung cancer. Owing to the presence of respiratory dysfunction and other diseases (bipolar affective disorder), the policy was to follow up without treatment. Fig. 1 a Positron emission tomography showing an accumulation of 18 F-fluorodeoxyglucose in a mass in the right breast, with a maximum standardized uptake value of 3.11. b Breast ultrasonography showed a well-demarcated tumor lesion, a slightly heterogeneous internal echo, and no enhancement of the posterior echo. c Color Doppler showed some internal blood flow. d T2-weighted images showing high intensity throughout the mass in the upper lateral region of the right breast. e T1-weighted gadolinium-enhanced magnetic resonance imaging showing a 2.2-cm-sized smooth-edged mass with early contrast-enhanced margin staining. f In the late contrast-enhanced phase, the entire mass is stained and the contrast agent is pooled
3.740234
0.980957
sec[1]/p[0]
en
0.999996
37027101
https://doi.org/10.1186/s40792-023-01633-8
[ "breast", "nodule", "lobe", "lung", "enhanced", "contrast", "tomography", "accumulation", "maximum", "standardized" ]
[ { "code": "GB23", "title": "Certain specified disorders of breast" }, { "code": "GB21.Z", "title": "Inflammatory disorders of breast, unspecified" }, { "code": "GB21.Y", "title": "Other specified inflammatory disorders of breast" }, { "code": "QF01.0", "title": "Acquired absence of breast" }, { "code": "GB23.3", "title": "Atrophy of breast" }, { "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" } ]
=== ICD-11 CODES FOUND === [GB23] Certain specified disorders of breast Definition: Any disorder of the breast or breast tissue, characterised by pathological changes, not classified elsewhere. Also known as: Certain specified disorders of breast | disease of breast | mastopathy [GB21.Z] Inflammatory disorders of breast, unspecified Also known as: Inflammatory disorders of breast, unspecified | Inflammatory disorders of breast | breast inflammation | inflammatory breast disease | mastitis NOS [GB21.Y] Other specified inflammatory disorders of breast Also known as: Other specified inflammatory disorders of breast | Breast antibioma | Infective mastitis | acute infective mastitis | nonpuerperal infective mastitis [QF01.0] Acquired absence of breast Also known as: Acquired absence of breast | absence of breast | mastectomy status | Acquired absence of breast, partial | Acquired absence of breast, total [GB23.3] Atrophy of breast Definition: A condition of the breast, caused by apoptosis of the cells commonly due to prolonged estrogen reduction, diminished cellular proliferation, decreased cellular volume, decreased function, ischaemia, malnutrition, disease, or mutation. This condition is characterised by a partial or complete decrease in size and function of the breast tissue. Also known as: Atrophy of breast | Hypoplasia of breast | hypoplastic breast | mammary hypoplasia [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 === GRAPH WALKS === --- Walk 1 --- [GB23] Certain specified disorders of breast Def: Any disorder of the breast or breast tissue, characterised by pathological changes, not classified elsewhere.... --CHILD--> [GB23.1] Fissure or fistula of nipple Def: A condition characterised by the formation of a deep furrow or crack-like lesion on the nipple and an abnormal passage between the nipple and adjacent tissues or surfaces.... --PARENT--> [GB23] Certain specified disorders of breast Def: Any disorder of the breast or breast tissue, characterised by pathological changes, not classified elsewhere.... --- Walk 2 --- [GB23] Certain specified disorders of breast Def: Any disorder of the breast or breast tissue, characterised by pathological changes, not classified elsewhere.... --PARENT--> [?] Disorders of breast Def: Any disorder characterised by pathological changes to the breast or breast tissue.... --CHILD--> [GB20] Benign breast disease Def: Any disease affecting females, characterised by benign, noncancerous lesions in the breast, leading to pathological changes to (and discomfort of) the breast or breast tissue.... --- Walk 3 --- [GB21.Z] Inflammatory disorders of breast, unspecified --PARENT--> [GB21] Inflammatory disorders of breast Def: Any disorder of the breast or breast tissue, characterised by inflammatory effects, pain, heat, redness, swelling, and loss of function.... --CHILD--> [GB21.0] Breast abscess Def: A condition of the breast, caused by inflammation due to infection with a bacterial or parasitic host, or contact with other foreign materials. This condition is characterised by a focal accumulation ... --- Walk 4 --- [GB21.Z] Inflammatory disorders of breast, unspecified --PARENT--> [GB21] Inflammatory disorders of breast Def: Any disorder of the breast or breast tissue, characterised by inflammatory effects, pain, heat, redness, swelling, and loss of function.... --CHILD--> [GB21.Y] Other specified inflammatory disorders of breast --- Walk 5 --- [GB21.Y] Other specified inflammatory disorders of breast --PARENT--> [GB21] Inflammatory disorders of breast Def: Any disorder of the breast or breast tissue, characterised by inflammatory effects, pain, heat, redness, swelling, and loss of function.... --CHILD--> [GB21.0] Breast abscess Def: A condition of the breast, caused by inflammation due to infection with a bacterial or parasitic host, or contact with other foreign materials. This condition is characterised by a focal accumulation ... --- Walk 6 --- [GB21.Y] Other specified inflammatory disorders of breast --PARENT--> [GB21] Inflammatory disorders of breast Def: Any disorder of the breast or breast tissue, characterised by inflammatory effects, pain, heat, redness, swelling, and loss of function.... --RELATED_TO--> [?] Nonpurulent mastitis associated with childbirth
[ "[GB23] Certain specified disorders of breast\n Def: Any disorder of the breast or breast tissue, characterised by pathological changes, not classified elsewhere....\n --CHILD--> [GB23.1] Fissure or fistula of nipple\n Def: A condition characterised by the formation of a deep furrow or crack-like lesion on the nipple and an abnormal passage between the nipple and adjacent tissues or surfaces....\n --PARENT--> [GB23] Certain specified disorders of breast\n Def: Any disorder of the breast or breast tissue, characterised by pathological changes, not classified elsewhere....", "[GB23] Certain specified disorders of breast\n Def: Any disorder of the breast or breast tissue, characterised by pathological changes, not classified elsewhere....\n --PARENT--> [?] Disorders of breast\n Def: Any disorder characterised by pathological changes to the breast or breast tissue....\n --CHILD--> [GB20] Benign breast disease\n Def: Any disease affecting females, characterised by benign, noncancerous lesions in the breast, leading to pathological changes to (and discomfort of) the breast or breast tissue....", "[GB21.Z] Inflammatory disorders of breast, unspecified\n --PARENT--> [GB21] Inflammatory disorders of breast\n Def: Any disorder of the breast or breast tissue, characterised by inflammatory effects, pain, heat, redness, swelling, and loss of function....\n --CHILD--> [GB21.0] Breast abscess\n Def: A condition of the breast, caused by inflammation due to infection with a bacterial or parasitic host, or contact with other foreign materials. This condition is characterised by a focal accumulation ...", "[GB21.Z] Inflammatory disorders of breast, unspecified\n --PARENT--> [GB21] Inflammatory disorders of breast\n Def: Any disorder of the breast or breast tissue, characterised by inflammatory effects, pain, heat, redness, swelling, and loss of function....\n --CHILD--> [GB21.Y] Other specified inflammatory disorders of breast", "[GB21.Y] Other specified inflammatory disorders of breast\n --PARENT--> [GB21] Inflammatory disorders of breast\n Def: Any disorder of the breast or breast tissue, characterised by inflammatory effects, pain, heat, redness, swelling, and loss of function....\n --CHILD--> [GB21.0] Breast abscess\n Def: A condition of the breast, caused by inflammation due to infection with a bacterial or parasitic host, or contact with other foreign materials. This condition is characterised by a focal accumulation ...", "[GB21.Y] Other specified inflammatory disorders of breast\n --PARENT--> [GB21] Inflammatory disorders of breast\n Def: Any disorder of the breast or breast tissue, characterised by inflammatory effects, pain, heat, redness, swelling, and loss of function....\n --RELATED_TO--> [?] Nonpurulent mastitis associated with childbirth" ]
GB23
Certain specified disorders of breast
[ { "from_icd11": "GB23", "icd10_code": "N6459", "icd10_title": "Other signs and symptoms in breast" }, { "from_icd11": "GB23", "icd10_code": "N6489", "icd10_title": "Other specified disorders of breast" }, { "from_icd11": "GB23", "icd10_code": "N6481", "icd10_title": "Ptosis of breast" }, { "from_icd11": "GB23", "icd10_code": "N6482", "icd10_title": "Hypoplasia of breast" }, { "from_icd11": "GB23", "icd10_code": "N6452", "icd10_title": "Nipple discharge" }, { "from_icd11": "GB23", "icd10_code": "N6451", "icd10_title": "Induration of breast" }, { "from_icd11": "GB23", "icd10_code": "N6453", "icd10_title": "Retraction of nipple" }, { "from_icd11": "GB23", "icd10_code": "N64", "icd10_title": "Other disorders of breast" }, { "from_icd11": "GB23", "icd10_code": "N648", "icd10_title": "Other specified disorders of breast" }, { "from_icd11": "GB23", "icd10_code": "N645", "icd10_title": "Other signs and symptoms in breast" }, { "from_icd11": "GB21.Z", "icd10_code": "N610", "icd10_title": "Mastitis without abscess" }, { "from_icd11": "GB21.Z", "icd10_code": "N611", "icd10_title": "Abscess of the breast and nipple" }, { "from_icd11": "GB21.Z", "icd10_code": "N61", "icd10_title": "Inflammatory disorders of breast" }, { "from_icd11": "QF01.0", "icd10_code": "Z9012", "icd10_title": "Acquired absence of left breast and nipple" }, { "from_icd11": "QF01.0", "icd10_code": "Z9011", "icd10_title": "Acquired absence of right breast and nipple" } ]
N6459
Other signs and symptoms in breast
At the age of 2.5 years she presented difficulty walking, we evidenced a dysmetria of lower limbs without other clinical signs and consequently we performed a X-ray of the lower limbs, which showed a congenital right coxa vara and the necessity for surgical intervention of osteostomy. At the age of 6, in consequence to a minor trauma at home, she had a fracture of the femur that needed surgical reduction. On this occasion DXA scan showed a mild reduction of bone mineral density (Z-score: -1.2) and markers of bone turnover were increased (CTX 1.55 ng/mL, normal range for age: 0.20–1.25 ng/mL; osteocalcin 17.7 nmol/L, normal range for age: 3.7–14.9 nmol/L). As far as bone alterations are concerned, she presented metaphyseal irregularity with widening of the growth plate at knees and at wrists’ level. Moreover, she presented a tubular appearance of metacarpals that became more evident over time . The last DXA scan at the age of 12 years was normal (femur BMD 1.002 g/cm 2 [Z-score: 1.5]; column BMD 0.947 g/cm 2 [Z-score: 0.7]) but markers of bone turnover were still high (CTX 3.21 ng/mL, normal range for age: 0.15–2.29 ng/mL; osteocalcin 25.2 nmol/L, normal range for age and sex: 2.2–20.4 nmol/L). Fig. 2 Bone abnormalities. A Pelvic X-ray of our patient evidenced right coxa vara. B Evolution of bone age through years. The progressive shape change of metacarpals that took a tubular form appears evident
4.097656
0.929199
sec[1]/sec[1]/p[1]
en
0.999997
35197096
https://doi.org/10.1186/s13023-022-02252-6
[ "bone", "range", "nmol", "that", "score", "evidenced", "limbs", "coxa", "vara", "femur" ]
[ { "code": "FC0Z", "title": "Diseases of the musculoskeletal system or connective tissue, unspecified" }, { "code": "FB84.Z", "title": "Osteomyelitis or osteitis, unspecified" }, { "code": "FB80.Z", "title": "Disorder of bone density or structure, unspecified" }, { "code": "FB86.11", "title": "Hypertrophy of bone" }, { "code": "FB86.1Z", "title": "Bone hyperplasias, unspecified" }, { "code": "QA00.6Y", "title": "Other specified examination of eyes or vision" }, { "code": "4B00.0Z", "title": "Neutropaenia, unspecified" }, { "code": "3B63.1Z", "title": "Acquired thrombocytosis, unspecified" }, { "code": "MA14.1C", "title": "Raised antibody titre" }, { "code": "BD11.1", "title": "Left ventricular failure with mid range ejection fraction" } ]
=== ICD-11 CODES FOUND === [FC0Z] Diseases of the musculoskeletal system or connective tissue, unspecified Also known as: Diseases of the musculoskeletal system or connective tissue, unspecified | bone disease NOS | bone disorder NOS | bone lesion NOS | musculoskeletal complications NOS [FB84.Z] Osteomyelitis or osteitis, unspecified Also known as: Osteomyelitis or osteitis, unspecified | Osteomyelitis or osteitis | bone inflammation | bone ulcer | bone inflammatory disease [FB80.Z] Disorder of bone density or structure, unspecified Also known as: Disorder of bone density or structure, unspecified | Certain specified disorders of bone density or structure [FB86.11] Hypertrophy of bone Also known as: Hypertrophy of bone | bone thickening | periosteum thickening | Infantile cortical hyperostoses | Post traumatic subperiosteal ossification [FB86.1Z] Bone hyperplasias, unspecified Also known as: Bone hyperplasias, unspecified | Bone hyperplasias [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 [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 [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 === GRAPH WALKS === --- Walk 1 --- [FC0Z] Diseases of the musculoskeletal system or connective tissue, unspecified --PARENT--> [15] Diseases of the musculoskeletal system or connective tissue Def: This chapter contains diseases of musculoskeletal system and diseases of connective tissue.... --RELATED_TO--> [?] Nonorgan specific systemic autoimmune disorders --- Walk 2 --- [FC0Z] Diseases of the musculoskeletal system or connective tissue, unspecified --PARENT--> [15] Diseases of the musculoskeletal system or connective tissue Def: This chapter contains diseases of musculoskeletal system and diseases of connective tissue.... --RELATED_TO--> [?] Symptoms, signs or clinical findings of the musculoskeletal system --- Walk 3 --- [FB84.Z] Osteomyelitis or osteitis, unspecified --PARENT--> [FB84] Osteomyelitis or osteitis --EXCLUDES--> [?] Inflammatory conditions of jaws --- Walk 4 --- [FB84.Z] Osteomyelitis or osteitis, unspecified --PARENT--> [FB84] Osteomyelitis or osteitis --CHILD--> [FB84.2] Subacute osteomyelitis --- Walk 5 --- [FB80.Z] Disorder of bone density or structure, unspecified --PARENT--> [FB80] Certain specified disorders of bone density or structure --CHILD--> [FB80.2] Osteitis condensans --- Walk 6 --- [FB80.Z] Disorder of bone density or structure, unspecified --PARENT--> [FB80] Certain specified disorders of bone density or structure --EXCLUDES--> [?] Osteopetrosis Def: Osteopetrosis ('marble bone disease') is a descriptive term that refers to a group of rare, heritable disorders of the skeleton characterised by increased bone density on radiographs. Osteopetrotic co...
[ "[FC0Z] Diseases of the musculoskeletal system or connective tissue, unspecified\n --PARENT--> [15] Diseases of the musculoskeletal system or connective tissue\n Def: This chapter contains diseases of musculoskeletal system and diseases of connective tissue....\n --RELATED_TO--> [?] Nonorgan specific systemic autoimmune disorders", "[FC0Z] Diseases of the musculoskeletal system or connective tissue, unspecified\n --PARENT--> [15] Diseases of the musculoskeletal system or connective tissue\n Def: This chapter contains diseases of musculoskeletal system and diseases of connective tissue....\n --RELATED_TO--> [?] Symptoms, signs or clinical findings of the musculoskeletal system", "[FB84.Z] Osteomyelitis or osteitis, unspecified\n --PARENT--> [FB84] Osteomyelitis or osteitis\n --EXCLUDES--> [?] Inflammatory conditions of jaws", "[FB84.Z] Osteomyelitis or osteitis, unspecified\n --PARENT--> [FB84] Osteomyelitis or osteitis\n --CHILD--> [FB84.2] Subacute osteomyelitis", "[FB80.Z] Disorder of bone density or structure, unspecified\n --PARENT--> [FB80] Certain specified disorders of bone density or structure\n --CHILD--> [FB80.2] Osteitis condensans", "[FB80.Z] Disorder of bone density or structure, unspecified\n --PARENT--> [FB80] Certain specified disorders of bone density or structure\n --EXCLUDES--> [?] Osteopetrosis\n Def: Osteopetrosis ('marble bone disease') is a descriptive term that refers to a group of rare, heritable disorders of the skeleton characterised by increased bone density on radiographs. Osteopetrotic co..." ]
FC0Z
Diseases of the musculoskeletal system or connective tissue, unspecified
[ { "from_icd11": "FC0Z", "icd10_code": "XIII", "icd10_title": "" }, { "from_icd11": "FB84.Z", "icd10_code": "M86672", "icd10_title": "Other chronic osteomyelitis, left ankle and foot" }, { "from_icd11": "FB84.Z", "icd10_code": "M86172", "icd10_title": "Other acute osteomyelitis, left ankle and foot" }, { "from_icd11": "FB84.Z", "icd10_code": "M86171", "icd10_title": "Other acute osteomyelitis, right ankle and foot" }, { "from_icd11": "FB84.Z", "icd10_code": "M86671", "icd10_title": "Other chronic osteomyelitis, right ankle and foot" }, { "from_icd11": "FB84.Z", "icd10_code": "M868X7", "icd10_title": "Other osteomyelitis, ankle and foot" }, { "from_icd11": "FB84.Z", "icd10_code": "M868X8", "icd10_title": "Other osteomyelitis, other site" }, { "from_icd11": "FB84.Z", "icd10_code": "M868X6", "icd10_title": "Other osteomyelitis, lower leg" }, { "from_icd11": "FB84.Z", "icd10_code": "M868X9", "icd10_title": "Other osteomyelitis, unspecified sites" }, { "from_icd11": "FB84.Z", "icd10_code": "M8668", "icd10_title": "Other chronic osteomyelitis, other site" }, { "from_icd11": "FB84.Z", "icd10_code": "M86662", "icd10_title": "Other chronic osteomyelitis, left tibia and fibula" }, { "from_icd11": "FB84.Z", "icd10_code": "M86151", "icd10_title": "Other acute osteomyelitis, right femur" }, { "from_icd11": "FB84.Z", "icd10_code": "M86141", "icd10_title": "Other acute osteomyelitis, right hand" }, { "from_icd11": "FB84.Z", "icd10_code": "M86641", "icd10_title": "Other chronic osteomyelitis, right hand" }, { "from_icd11": "FB84.Z", "icd10_code": "M8669", "icd10_title": "Other chronic osteomyelitis, multiple sites" } ]
XIII
Bone stock was assessed and an Exeter Stem long enough to bypass the bony defect and achieve adequate fixation was selected (range 205-260 mm). This was implanted with cement that had been modified by the addition of antibiotics. The cement was either hand packed or injected into the femoral canal and directly applied to the implant. Finger pressurisation was used upon stem insertion. Acetabulum reconstruction was undertaken using a size F Trident insert (after burring the back to gain stability within the cement mantle), a RimFit cup or the Exeter Contemporary flanged cup (all Stryker Orthopedics). To maximise stability, a 36 mm inner diameter was chosen. In the presence of severe acetabular bone loss, screws and wires were inserted into the pelvis to act as a scaffold to ensure adequacy of the cement mantle. Post-operative intravenous and/or oral antibiotics were given for a minimum of 6 weeks . Patients were allowed to weight bear as tolerated post-operatively. Fig. 1 a Pre-operative Anteroposterior (AP) radiograph showing a modular fluted revision femoral stem and cup-cage acetabular construct which were proven to be infected by tissue diagnosis ( b ) AP radiograph after 1 year of explantation of infected prothesis and treatment with a long CUMAR technique ( c ) AP radiograph 4.5 years post-operatively demonstrating continued survival of the 1st stage with complete eradication of the infection
3.951172
0.686523
sec[1]/p[2]
en
0.999996
33863329
https://doi.org/10.1186/s12891-021-04237-1
[ "cement", "stem", "radiograph", "bone", "exeter", "long", "antibiotics", "femoral", "stability", "mantle" ]
[ { "code": "DA07.5", "title": "Cementum dysplasia" }, { "code": "2E83.1", "title": "Benign osteogenic tumours of bone or articular cartilage of lower jaw" }, { "code": "DA08.0&XA4KC7", "title": "Caries of cementum" }, { "code": "LA05.Y", "title": "Other specified cerebral structural developmental anomalies" }, { "code": "8B81.0", "title": "Brainstem lesion" }, { "code": "1D04.1Y&XA8AT9", "title": "Brainstem granuloma" }, { "code": "8A40.Z", "title": "Multiple sclerosis, unspecified" }, { "code": "8D43.0Z", "title": "Encephalopathy due to toxicity, unspecified" }, { "code": "FC0Z", "title": "Diseases of the musculoskeletal system or connective tissue, unspecified" }, { "code": "FB84.Z", "title": "Osteomyelitis or osteitis, unspecified" } ]
=== ICD-11 CODES FOUND === [DA07.5] Cementum dysplasia Also known as: Cementum dysplasia | Cementum hyperplasia | cementation hyperplasia | Hypercementosis | cementosis [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 [LA05.Y] Other specified cerebral structural developmental anomalies Also known as: Other specified cerebral structural developmental anomalies | Aprosencephaly | Garcia-Lurie syndrome | Atelencephaly | Brain stem dysplasia [8B81.0] Brainstem lesion Also known as: Brainstem lesion [8A40.Z] Multiple sclerosis, unspecified Also known as: Multiple sclerosis, unspecified | Multiple sclerosis | cerebrospinal sclerosis | disseminated sclerosis | generalised multiple sclerosis [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 [FC0Z] Diseases of the musculoskeletal system or connective tissue, unspecified Also known as: Diseases of the musculoskeletal system or connective tissue, unspecified | bone disease NOS | bone disorder NOS | bone lesion NOS | musculoskeletal complications NOS [FB84.Z] Osteomyelitis or osteitis, unspecified Also known as: Osteomyelitis or osteitis, unspecified | Osteomyelitis or osteitis | bone inflammation | bone ulcer | bone inflammatory disease === GRAPH WALKS === --- Walk 1 --- [DA07.5] Cementum dysplasia --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.... --CHILD--> [DA07.3] Disturbances in tooth formation Def: A group of conditions characterised by disturbances in tooth formation.... --- Walk 2 --- [DA07.5] Cementum dysplasia --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.... --PARENT--> [?] Diseases or disorders of orofacial complex Def: Morbid process, derangement or abnormality localised in the mouth or related tissues of the face... --- Walk 3 --- [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 4 --- [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... --CHILD--> [2E83.0] Benign osteogenic tumours of bone or articular cartilage of skull or face --- Walk 5 --- [LA05.Y] Other specified cerebral structural developmental anomalies --PARENT--> [LA05] Cerebral structural developmental anomalies Def: Any condition caused by failure of the brain to correctly develop during the antenatal period.... --CHILD--> [LA05.0] Microcephaly Def: A condition caused by failure of the head to correctly develop during the antenatal period. This condition is characterised by a head size that is significantly smaller than normal for their age and s... --- Walk 6 --- [LA05.Y] Other specified cerebral structural developmental anomalies --PARENT--> [LA05] Cerebral structural developmental anomalies Def: Any condition caused by failure of the brain to correctly develop during the antenatal period.... --EXCLUDES--> [?] Encephalocele
[ "[DA07.5] Cementum dysplasia\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....\n --CHILD--> [DA07.3] Disturbances in tooth formation\n Def: A group of conditions characterised by disturbances in tooth formation....", "[DA07.5] Cementum dysplasia\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....\n --PARENT--> [?] Diseases or disorders of orofacial complex\n Def: Morbid process, derangement or abnormality localised in the mouth or related tissues of the face...", "[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 --CHILD--> [2E83.0] Benign osteogenic tumours of bone or articular cartilage of skull or face", "[LA05.Y] Other specified cerebral structural developmental anomalies\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--> [LA05.0] Microcephaly\n Def: A condition caused by failure of the head to correctly develop during the antenatal period. This condition is characterised by a head size that is significantly smaller than normal for their age and s...", "[LA05.Y] Other specified cerebral structural developmental anomalies\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" ]
DA07.5
Cementum dysplasia
[ { "from_icd11": "DA07.5", "icd10_code": "K034", "icd10_title": "Hypercementosis" }, { "from_icd11": "2E83.1", "icd10_code": "D165", "icd10_title": "Benign neoplasm of lower jaw bone" }, { "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": "8D43.0Z", "icd10_code": "G92", "icd10_title": "Toxic encephalopathy" }, { "from_icd11": "FC0Z", "icd10_code": "XIII", "icd10_title": "" }, { "from_icd11": "FB84.Z", "icd10_code": "M86672", "icd10_title": "Other chronic osteomyelitis, left ankle and foot" }, { "from_icd11": "FB84.Z", "icd10_code": "M86172", "icd10_title": "Other acute osteomyelitis, left ankle and foot" }, { "from_icd11": "FB84.Z", "icd10_code": "M86171", "icd10_title": "Other acute osteomyelitis, right ankle and foot" }, { "from_icd11": "FB84.Z", "icd10_code": "M86671", "icd10_title": "Other chronic osteomyelitis, right ankle and foot" }, { "from_icd11": "FB84.Z", "icd10_code": "M868X7", "icd10_title": "Other osteomyelitis, ankle and foot" }, { "from_icd11": "FB84.Z", "icd10_code": "M868X8", "icd10_title": "Other osteomyelitis, other site" }, { "from_icd11": "FB84.Z", "icd10_code": "M868X6", "icd10_title": "Other osteomyelitis, lower leg" }, { "from_icd11": "FB84.Z", "icd10_code": "M868X9", "icd10_title": "Other osteomyelitis, unspecified sites" } ]
K034
Hypercementosis
A full-term male newborn with a round-shaped defect at the vertex of the scalp and skull (dimensions, 8 cm × 9 cm) was was born in the Obstetrics Department of Zhongshan Hospital Affiliated with Sun Yat-Sen University (also known as Zhongshan City People's Hospital) on May 10, 2019 . The infant weighed 2.5 kg (−2SD) (38 weeks gestational age). The height of the infant was 48.6 cm (−1SD). Th head circumference was 33.2 cm (–1SD). The infant's mother experienced premature rupture of amniotic membrane for 11 h prior to giving birth and had gestational diabetes mellitus. Her examination showed no placental abnormalities, and no herpes simplex, varicella-zoster, rubella, or cytomegalovirus infections. The mother denied having been exposed to teratogenic drugs, radiation, or chemicals during pregnancy. The pregnancy of his mother was G1P1. There was no history of hypertensive disorder complicating pregnancy. There were no family histories of aplasia cutis congenita and other congenital malformations.The Apgar score of the infant was 10 at 1, 5, and 10 min after birth. He had no congenital malformation of the digestive tract, nor skeletal or congenital heart malformations. Peripheral blood, white blood cell, and blood gas analyses, as well as lactic acid, serum C-reactive protein, blood ammonia, and hepatobiliary biochemistry test results, were all normal. The blood cultures revealed no bacterial growth.
3.900391
0.982422
sec[1]/p[0]
en
0.999996
PMC9874222
https://doi.org/10.3389/fsurg.2022.1072021
[ "blood", "mother", "pregnancy", "congenital", "zhongshan", "gestational", "birth", "malformations", "full", "term" ]
[ { "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": "QA48.1", "title": "Care or examination of lactating mother" }, { "code": "KB60.1", "title": "Syndrome of infant of a diabetic mother, type 1 or 2, nongestational, insulin dependent" }, { "code": "1C1D.0", "title": "Primary yaws" }, { "code": "KD35", "title": "Neonatal withdrawal syndrome from maternal use of drugs of addiction" }, { "code": "KB60.0", "title": "Syndrome of infant of mother with gestational diabetes" } ]
=== 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 [QA48.1] Care or examination of lactating mother Also known as: Care or examination of lactating mother | care of lactating mother | examination of lactating mother | supervision of lactation | supervision of breastfeeding Excludes: Certain specified disorders of breast or lactation associated with childbirth [KB60.1] Syndrome of infant of a diabetic mother, type 1 or 2, nongestational, insulin dependent Definition: 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, birth injuries, congenital anomalies, hypoglycaemia, respiratory distress, caudal regression syndrome and hypertrophic cardiomyopathy. Also known as: Syndrome of infant of a diabetic mother, type 1 or 2, nongestational, insulin dependent | infant of a diabetic mother syndrome | maternal diabetes syndrome | syndrome of infant of diabetic mother | infant of diabetic mother [1C1D.0] Primary yaws Definition: Primary yaws results from primary inoculation of Treponema pallidum subsp. pertenue into the skin, manifesting 2-12 weeks later as a localised papule (initial, primary or ‘mother' yaw) before developing into a large non-tender ulcerating nodule, often resembling a raspberry (hence the name ‘framboesia’). The primary lesion is most commonly located on the legs and ankles may also be found on the buttocks, arms, hands, and face. It usually heals after 3–6 months and is still present at the onset o Also known as: Primary yaws | Chancre of yaws | Primary framboesia | initial lesions of yaws | mother yaw Includes: Chancre of yaws | Primary framboesia [KD35] Neonatal withdrawal syndrome from maternal use of drugs of addiction Definition: Intrauterine exposure to addictive drugs can lead to neonatal withdrawal symptoms. Withdrawal symptoms are usually neurological, preventing normal autonomic function. The clinical presentation of drug withdrawal is variable and dependent on several factors, such as, the type and dose of drug used and rate of metabolism and excretion of the mother and infant. Also known as: Neonatal withdrawal syndrome from maternal use of drugs of addiction | Drug withdrawal syndrome in infant of dependent mother | Neonatal abstinence syndrome | drug withdrawal syndrome in newborn | neonatal drug withdrawal syndrome Includes: Drug withdrawal syndrome in infant of dependent mother | Neonatal abstinence syndrome Excludes: Fetus or newborn affected by maternal anaesthesia or analgesia in pregnancy, labour or delivery [KB60.0] Syndrome of infant of mother with gestational diabetes Definition: 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 effects include macrosomia, intrauterine growth restriction, birth injuries, congenital anomalies, hypoglycaemia, respiratory distress, and hypertrophic cardiomyopathy. Also known as: Syndrome of infant of mother with gestational diabetes | infant of mother with gestational diabetes | IGDM - [infant of gestational diabetic mother] | Fetus or newborn with hypoglycaemia affected by maternal gestational diabetes | Fetus or newborn affected by maternal gestational diabetes === 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.... --RELATED_TO--> [?] Symptoms, signs or clinical findings of blood, blood-forming organs, or the immune system --- Walk 2 --- [3C0Z] Diseases of the blood or blood-forming organs, unspecified --PARENT--> [03] Diseases of the blood or blood-forming organs Def: This chapter includes diseases of the blood as well as diseases of blood forming organs.... --CHILD--> [?] Coagulation defects, purpura or other haemorrhagic or related conditions Def: A condition caused by determinants arising during the antenatal period, after birth or by genetically inherited factors, leading to coagulation defects. This condition is characterised by increased br... --- Walk 3 --- [MF50.4Z] Haematuria, unspecified --PARENT--> [MF50.4] Haematuria Def: Hematuria means presence of blood or red blood cells (RBCs) in the urine. There are two types of hematuria: gross hematuria (when one can see the blood in the urine) and microscopic hematuria (when th... --CHILD--> [MF50.41] Microscopic haematuria --- Walk 4 --- [MF50.4Z] Haematuria, unspecified --PARENT--> [MF50.4] Haematuria Def: Hematuria means presence of blood or red blood cells (RBCs) in the urine. There are two types of hematuria: gross hematuria (when one can see the blood in the urine) and microscopic hematuria (when th... --CHILD--> [MF50.4Z] Haematuria, unspecified --- Walk 5 --- [MA12.1] Finding of cocaine in blood --PARENT--> [MA12] Clinical findings of drugs, medicaments and biological substances in blood, blood-forming organs, or the immune system --PARENT--> [?] Clinical findings in blood, blood-forming organs, or the immune system --- Walk 6 --- [MA12.1] Finding of cocaine in blood --PARENT--> [MA12] Clinical findings of drugs, medicaments and biological substances in blood, blood-forming organs, or the immune system --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 --RELATED_TO--> [?] Symptoms, signs or clinical findings of blood, blood-forming organs, or the immune system", "[3C0Z] Diseases of the blood or blood-forming organs, unspecified\n --PARENT--> [03] Diseases of the blood or blood-forming organs\n Def: This chapter includes diseases of the blood as well as diseases of blood forming organs....\n --CHILD--> [?] Coagulation defects, purpura or other haemorrhagic or related conditions\n Def: A condition caused by determinants arising during the antenatal period, after birth or by genetically inherited factors, leading to coagulation defects. This condition is characterised by increased br...", "[MF50.4Z] Haematuria, unspecified\n --PARENT--> [MF50.4] Haematuria\n Def: Hematuria means presence of blood or red blood cells (RBCs) in the urine. There are two types of hematuria: gross hematuria (when one can see the blood in the urine) and microscopic hematuria (when th...\n --CHILD--> [MF50.41] Microscopic haematuria", "[MF50.4Z] Haematuria, unspecified\n --PARENT--> [MF50.4] Haematuria\n Def: Hematuria means presence of blood or red blood cells (RBCs) in the urine. There are two types of hematuria: gross hematuria (when one can see the blood in the urine) and microscopic hematuria (when th...\n --CHILD--> [MF50.4Z] Haematuria, unspecified", "[MA12.1] Finding of cocaine in blood\n --PARENT--> [MA12] Clinical findings of drugs, medicaments and biological substances in blood, blood-forming organs, or the immune system\n --PARENT--> [?] Clinical findings in blood, blood-forming organs, or the immune system", "[MA12.1] Finding of cocaine in blood\n --PARENT--> [MA12] Clinical findings of drugs, medicaments and biological substances in blood, blood-forming organs, or the immune system\n --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
A 63-year-old woman with a 20-year history of progressive symmetrical muscle weakness was admitted to our department. She complained of difficulty squatting and climbing stairs accompanied by myalgia at 43 years of age and weakness of the arms at 46 years of age. Her medical history was unremarkable except for a 10-year history of hypertension. On admission, the physical examination revealed symmetrical muscle weakness of the proximal limbs and neck muscles and postural tremor of the head and hands. Mental status examination evaluated normal cerebral cognitive function. The serum creatine kinase level was mildly elevated. Electrophysiological study revealed the myopathic pattern in the muscles with decreased nerve conduction velocity of the bilateral median nerves. Mini-Mental State Examination and Montreal Cognitive Assessment at 60 years of age revealed no cognitive impairment. Findings on muscle MRI were characteristic of fatty infiltration and atrophy of the hip and thigh muscles. Muscle biopsy showed both myopathic changes including rimmed and non-rimmed vacuoles in some fibers and neurogenic changes with fiber-type grouping and group atrophy. Oil Red O staining showed only a mild increase of lipid droplets . Next-generation sequencing revealed no pathogenic variants in the myopathy-related genes. The patient had been misdiagnosed with limb-girdle muscular dystrophy or lipid storage myopathy.
4.066406
0.979004
sec[2]/sec[3]/sec[0]/p[0]
en
0.999996
PMC9798416
https://doi.org/10.3389/fneur.2022.1085283
[ "muscle", "weakness", "muscles", "cognitive", "symmetrical", "mental", "myopathic", "atrophy", "changes", "rimmed" ]
[ { "code": "FB3Z", "title": "Disorders of muscles, unspecified" }, { "code": "FB32.Y", "title": "Other specified disorders of muscles" }, { "code": "8C70.Z", "title": "Muscular dystrophy, unspecified" }, { "code": "FB32.2Z", "title": "Ischaemic infarction of muscle, unspecified" }, { "code": "FB56.2", "title": "Myalgia" }, { "code": "MG22", "title": "Fatigue" }, { "code": "MB5Z", "title": "Paralytic symptoms, unspecified" }, { "code": "FA31.5", "title": "Acquired pes planus" }, { "code": "MF50.2Y", "title": "Other specified urinary incontinence" }, { "code": "MB21.Z", "title": "Symptoms, signs or clinical findings involving cognition, unspecified" } ]
=== ICD-11 CODES FOUND === [FB3Z] Disorders of muscles, unspecified Also known as: Disorders of muscles, unspecified | disorder of muscle, unspecified | muscle disease | muscular disease | muscular disorder [FB32.Y] Other specified disorders of muscles Also known as: Other specified disorders of muscles | Muscle wasting or atrophy, not elsewhere classified | muscle wasting | muscle wasting disorder | Sarcopenia [8C70.Z] Muscular dystrophy, unspecified Also known as: Muscular dystrophy, unspecified | Muscular dystrophy | Gower's muscular dystrophy | progressive musclular dystrophy | pseudohypertrophic atrophy [FB32.2Z] Ischaemic infarction of muscle, unspecified Also known as: Ischaemic infarction of muscle, unspecified | Ischaemic infarction of muscle | muscle infarction [FB56.2] Myalgia Definition: This is a disorder characterised by pain in a muscle or group of muscles. Also known as: Myalgia | muscle ache | muscle soreness | muscular pain | myalgic Excludes: Chronic primary musculoskeletal pain | Chronic secondary musculoskeletal pain [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 [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 [MF50.2Y] Other specified urinary incontinence Also known as: Other specified urinary incontinence | Overflow Incontinence | Extraurethral urinary incontinence | Dribbling of urine | Urethra sphincter incontinence [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 === GRAPH WALKS === --- Walk 1 --- [FB3Z] Disorders of muscles, unspecified --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 2 --- [FB3Z] Disorders of muscles, unspecified --PARENT--> [?] Disorders of muscles --CHILD--> [FB32] Certain specified disorders of muscle Def: This is an impairment of health or a condition of abnormal functioning of the muscle that does not fit in another category.... --- Walk 3 --- [FB32.Y] Other specified disorders of muscles --PARENT--> [FB32] Certain specified disorders of muscle Def: This is an impairment of health or a condition of abnormal functioning of the muscle that does not fit in another category.... --EXCLUDES--> [?] Alcoholic myopathy Def: Myopathy secondary to alcohol use and includes acute and chronic alcoholic myopathy. Several forms have been described: acute necrotizing myopathy, acute hypokalaemic myopathy, chronic alcoholic myopa... --- Walk 4 --- [FB32.Y] Other specified disorders of muscles --PARENT--> [FB32] Certain specified disorders of muscle Def: This is an impairment of health or a condition of abnormal functioning of the muscle that does not fit in another category.... --CHILD--> [FB32.1] Spontaneous rupture of muscle Def: This is a spontaneous tearing or separation of muscle fibres from other muscle fibres and/or tendons in the absence of trauma.... --- Walk 5 --- [8C70.Z] Muscular dystrophy, unspecified --PARENT--> [8C70] 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... --RELATED_TO--> [?] Barth syndrome Def: Barth syndrome is an inborn error of phospholipid metabolism characterised by dilated cardiomyopathy (DCM), skeletal myopathy, neutropaenia, growth delay and organic aciduria.... --- Walk 6 --- [8C70.Z] Muscular dystrophy, unspecified --PARENT--> [8C70] 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... --CHILD--> [8C70.2] Emery-Dreifuss muscular dystrophy Def: Emery-Dreifuss muscular dystrophy (EDMD) is a muscle disease characterised by muscular weakness and atrophy, with early contractures of the tendons and cardiac involvement (arrhythmias, cardiomyopathy...
[ "[FB3Z] Disorders of muscles, unspecified\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...", "[FB3Z] Disorders of muscles, unspecified\n --PARENT--> [?] Disorders of muscles\n --CHILD--> [FB32] Certain specified disorders of muscle\n Def: This is an impairment of health or a condition of abnormal functioning of the muscle that does not fit in another category....", "[FB32.Y] Other specified disorders of muscles\n --PARENT--> [FB32] Certain specified disorders of muscle\n Def: This is an impairment of health or a condition of abnormal functioning of the muscle that does not fit in another category....\n --EXCLUDES--> [?] Alcoholic myopathy\n Def: Myopathy secondary to alcohol use and includes acute and chronic alcoholic myopathy. Several forms have been described: acute necrotizing myopathy, acute hypokalaemic myopathy, chronic alcoholic myopa...", "[FB32.Y] Other specified disorders of muscles\n --PARENT--> [FB32] Certain specified disorders of muscle\n Def: This is an impairment of health or a condition of abnormal functioning of the muscle that does not fit in another category....\n --CHILD--> [FB32.1] Spontaneous rupture of muscle\n Def: This is a spontaneous tearing or separation of muscle fibres from other muscle fibres and/or tendons in the absence of trauma....", "[8C70.Z] Muscular dystrophy, unspecified\n --PARENT--> [8C70] 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...\n --RELATED_TO--> [?] Barth syndrome\n Def: Barth syndrome is an inborn error of phospholipid metabolism characterised by dilated cardiomyopathy (DCM), skeletal myopathy, neutropaenia, growth delay and organic aciduria....", "[8C70.Z] Muscular dystrophy, unspecified\n --PARENT--> [8C70] 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...\n --CHILD--> [8C70.2] Emery-Dreifuss muscular dystrophy\n Def: Emery-Dreifuss muscular dystrophy (EDMD) is a muscle disease characterised by muscular weakness and atrophy, with early contractures of the tendons and cardiac involvement (arrhythmias, cardiomyopathy..." ]
FB3Z
Disorders of muscles, unspecified
[ { "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" }, { "from_icd11": "FB3Z", "icd10_code": "M6088", "icd10_title": "Other myositis, other site" }, { "from_icd11": "FB3Z", "icd10_code": "M60862", "icd10_title": "Other myositis, left lower leg" }, { "from_icd11": "FB3Z", "icd10_code": "M60861", "icd10_title": "Other myositis, right lower leg" }, { "from_icd11": "FB3Z", "icd10_code": "M6089", "icd10_title": "Other myositis, multiple sites" }, { "from_icd11": "FB3Z", "icd10_code": "M60852", "icd10_title": "Other myositis, left thigh" }, { "from_icd11": "FB3Z", "icd10_code": "M60821", "icd10_title": "Other myositis, right upper arm" }, { "from_icd11": "FB3Z", "icd10_code": "M60871", "icd10_title": "Other myositis, right ankle and foot" }, { "from_icd11": "FB3Z", "icd10_code": "M60812", "icd10_title": "Other myositis, left shoulder" } ]
M60831
Other myositis, right forearm
In our patient, amoebic dysentery was initially treated by iv Metronidazole due to the poor clinical conditions with impossibility of oral administration. Metronidazole has been used for the treatment of gastrointestinal infections for >50 years . Metronidazole is considered to be a cost-effective drug because of its low cost, good activity against pathogenic anaerobic bacteria and protozoa, favorable pharmacokinetic and pharmacodynamic properties and minor adverse effects. However, several mechanisms of resistance to Metronidazole in anaerobic bacteria have been proposed. These mechanisms differ among organisms, but the primary basis for resistance is decreased uptake of the drug or altered reduction efficiency . Moreover, the normal microflora serve as a reservoir of antibiotic-resistance determinants, where some dissemination of resistance can occur. The impact of Metronidazole on the normal microflora varies depending on the body site involved. In addition to Metronidazole, the use of fluids was of key importance to restore hydration and prevent dehydration. The management of dehydration in malnourished children is different from that recommended in well-nourished children, as they need special alternative fluids to avoid electrolyte imbalances and fluid overload . In this case, rehydration therapy included both bolus of 1/2 normal saline + 1/2 dextrose 5% and oral ReSoMal alternated with F75.
4.300781
0.795898
sec[2]/p[2]
en
0.999995
36677457
https://doi.org/10.3390/microorganisms11010165
[ "metronidazole", "resistance", "oral", "cost", "drug", "anaerobic", "bacteria", "mechanisms", "microflora", "fluids" ]
[ { "code": "MG55.0", "title": "Artemisinin resistant Plasmodium falciparum" }, { "code": "5A74.Y", "title": "Other specified adrenocortical insufficiency" }, { "code": "5A44", "title": "Insulin-resistance syndromes" }, { "code": "LD2A.4", "title": "46,XY disorder of sex development due to androgen resistance" }, { "code": "LB45.1", "title": "46,XX gonadal dysgenesis" }, { "code": "MD11.8Z", "title": "Mouth breathing, unspecified" }, { "code": "DA01.00", "title": "Oral leukoplakia" }, { "code": "DA01.10", "title": "Oral aphthae or aphtha-like ulceration" }, { "code": "MD80.1", "title": "Symptom or complaint of the mouth, tongue or lip" }, { "code": "DA01.1Y", "title": "Other specified noninfectious erosive or ulcerative disorders of oral mucosa" } ]
=== ICD-11 CODES FOUND === [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 [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 [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 [LD2A.4] 46,XY disorder of sex development due to androgen resistance Definition: Androgen insensitivity syndrome (AIS) is a disorder of sex development (DSD) characterised by the presence of female external genitalia, ambiguous genitalia or variable defects in virilization in a 46,XY individual with absent or partial responsiveness to age-appropriate levels of androgens. It comprises two clinical subgroups: complete AIS (CAIS) and partial AIS (PAIS). Also known as: 46,XY disorder of sex development due to androgen resistance | Androgen resistance syndrome | Testicular feminization syndrome | Androgen insensitivity syndrome | Goldberg-Maxwell syndrome [LB45.1] 46,XX gonadal dysgenesis Definition: Karyotype 46 XX; Gonads: gonadal dysgenesis (streak gonads); Phenotype female with symptoms like primary amenorrhea, hypergonadotropic hypogonadism, normal stature and no other abnormalities. Also known as: 46,XX gonadal dysgenesis | Follicular stimulating hormone-resistant ovaries | Resistant ovary syndrome | 46,XX pure gonadal dysgenesis | 46,XX complete gonadal dysgenesis [MD11.8Z] Mouth breathing, unspecified Also known as: Mouth breathing, unspecified | Mouth breathing | breathing orally | mouth respiration [DA01.00] Oral leukoplakia Definition: Leukoplakia is a condition where areas of keratosis appear as adherent white patches on the mucous membranes of the oral cavity. Leukoplakia may affect other gastrointestinal tract mucosal sites, or mucosal surfaces of the urinary tract and genitals. Also known as: Oral leukoplakia | Leukoplakia of gingiva | leukoplakia of oral epithelium | leucoplakia of oral mucosa | leukokeratosis of oral mucosa Includes: Leukoplakia of gingiva Excludes: Hairy leukoplakia [DA01.10] Oral aphthae or aphtha-like ulceration Definition: This is a frequent small, shallow, painful ulceration in the oral mucosa. Recurrent oral ulceration that clinically resembles recurrent aphthous stomatitis but presents atypically, including commencement after adolescence, with fever, with a strong family history, or failing to resolve with age. Also known as: Oral aphthae or aphtha-like ulceration | Recurrent aphthous stomatitis | Recurrent oral aphthae | Major recurrent aphthous stomatitis | major aphthous stomatitis [MD80.1] Symptom or complaint of the mouth, tongue or lip Also known as: Symptom or complaint of the mouth, tongue or lip | Mouth swelling | mouth oedema | swollen mouth | Lip swelling [DA01.1Y] Other specified noninfectious erosive or ulcerative disorders of oral mucosa Also known as: Other specified noninfectious erosive or ulcerative disorders of oral mucosa | Oral ulceration due to immunobullous disease | Oral mucosal involvement by immunobullous disorder classified elsewhere | Oral ulceration due to physical injury | Mechanical oral ulceration === GRAPH WALKS === --- Walk 1 --- [MG55.0] Artemisinin resistant Plasmodium falciparum --PARENT--> [MG55] Finding of parasite resistant to antimicrobial drugs --CHILD--> [MG55.0] Artemisinin resistant Plasmodium falciparum --- Walk 2 --- [MG55.0] Artemisinin resistant Plasmodium falciparum --PARENT--> [MG55] Finding of parasite resistant to antimicrobial drugs --CHILD--> [MG55.0] Artemisinin resistant Plasmodium falciparum --- Walk 3 --- [5A74.Y] Other specified adrenocortical insufficiency --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... --PARENT--> [?] Disorders of the adrenal glands or adrenal hormone system --- Walk 4 --- [5A74.Y] Other specified adrenocortical insufficiency --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--> [?] X-linked adrenoleukodystrophy Def: X-linked adrenoleukodystrophy (X-ALD) is a peroxisomal disease characterised by progressive demyelinisation of the central nervous system (CNS) (brain and/or spinal cord) and peripheral adrenal insuff... --- Walk 5 --- [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 6 --- [5A44] Insulin-resistance syndromes --PARENT--> [?] Other disorders of glucose regulation or pancreatic internal secretion --EXCLUDES--> [?] Benign neoplasm of endocrine pancreas
[ "[MG55.0] Artemisinin resistant Plasmodium falciparum\n --PARENT--> [MG55] Finding of parasite resistant to antimicrobial drugs\n --CHILD--> [MG55.0] Artemisinin resistant Plasmodium falciparum", "[MG55.0] Artemisinin resistant Plasmodium falciparum\n --PARENT--> [MG55] Finding of parasite resistant to antimicrobial drugs\n --CHILD--> [MG55.0] Artemisinin resistant Plasmodium falciparum", "[5A74.Y] Other specified adrenocortical insufficiency\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 --PARENT--> [?] Disorders of the adrenal glands or adrenal hormone system", "[5A74.Y] Other specified adrenocortical insufficiency\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--> [?] X-linked adrenoleukodystrophy\n Def: X-linked adrenoleukodystrophy (X-ALD) is a peroxisomal disease characterised by progressive demyelinisation of the central nervous system (CNS) (brain and/or spinal cord) and peripheral adrenal insuff...", "[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 --EXCLUDES--> [?] Benign neoplasm of endocrine pancreas" ]
MG55.0
Artemisinin resistant Plasmodium falciparum
[ { "from_icd11": "5A44", "icd10_code": "E10-E14", "icd10_title": "" }, { "from_icd11": "LD2A.4", "icd10_code": "E3450", "icd10_title": "Androgen insensitivity syndrome, unspecified" }, { "from_icd11": "LD2A.4", "icd10_code": "E3451", "icd10_title": "Complete androgen insensitivity syndrome" }, { "from_icd11": "LD2A.4", "icd10_code": "E345", "icd10_title": "Androgen insensitivity syndrome" }, { "from_icd11": "LB45.1", "icd10_code": "Q99", "icd10_title": "Other chromosome abnormalities, not elsewhere classified" }, { "from_icd11": "LB45.1", "icd10_code": "Q991", "icd10_title": "46, XX true hermaphrodite" }, { "from_icd11": "MD11.8Z", "icd10_code": "R065", "icd10_title": "Mouth breathing" }, { "from_icd11": "DA01.00", "icd10_code": "K1329", "icd10_title": "Other disturbances of oral epithelium, including tongue" }, { "from_icd11": "DA01.00", "icd10_code": "K1321", "icd10_title": "Leukoplakia of oral mucosa, including tongue" }, { "from_icd11": "DA01.00", "icd10_code": "K132", "icd10_title": "Leukoplakia and other disturbances of oral epithelium, including tongue" }, { "from_icd11": "DA01.10", "icd10_code": "K120", "icd10_title": "Recurrent oral aphthae" } ]
E10-E14
In summary, this report describes a case of iron dust lung with concomitant TB. To avoid further lung injury, such patients should be discontinued from occupational exposure. Regular and long-term monitoring is required for patients with a history of exposure to welding fumes, as the risk of TB in this group is significantly elevated, and this risk may be long-standing even if exposure is stopped. As with our patient, any typical but non-specific features of TB in patients with siderosis should be thoroughly examined, such as persistent cough, weight loss, and fever, to rule out TB. In addition, any radiological findings, such as asymmetrical nodules, rapid progression, or cavities, should be of concern. TB treatment in these patients may be prolonged because sputum specimens may remain smear-positive for a longer period. Finally, patients with siderosis should receive close and regular follow-up for early detection of any new TB cases or recurrences. When clinicians encounter such rare cases, while referring to the patient’s symptoms and imaging performance, a detailed understanding of the work history, combined with a variety of morphological results, such as conventional morphological examination of alveolar lavage fluid, alveolar lavage fluid pathological fluid-based examination, lung tissue biopsy and Prussian blue staining, etc., will be very helpful for diagnosis and differential diagnosis.
4.09375
0.927246
sec[3]/p[0]
en
0.999996
36816928
https://doi.org/10.3389/fonc.2023.1001802
[ "patients", "this", "lung", "exposure", "fluid", "regular", "long", "risk", "siderosis", "cases" ]
[ { "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": "4A01.03", "title": "Transient hypogammaglobulinaemia of infancy" }, { "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 === [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 [4A01.03] Transient hypogammaglobulinaemia of infancy Also known as: Transient hypogammaglobulinaemia of infancy | immunoglobulin maturational delay | THI - [transient hypogammaglobulinaemia of infancy] [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 --- [PL14.C] Patient received diagnostic test or treatment intended for another patient --EXCLUDES--> [?] Procedure undertaken at wrong site or wrong side, as mode of injury or harm --CHILD--> [?] Performance of inappropriate operation --- Walk 2 --- [PL14.C] Patient received diagnostic test or treatment intended for another patient --EXCLUDES--> [?] Procedure undertaken at wrong site or wrong side, as mode of injury or harm --EXCLUDES--> [?] Patient received diagnostic test or treatment intended for another patient --- Walk 3 --- [QB14] Unavailability or inaccessibility of health care facilities --EXCLUDES--> [?] Person awaiting admission to adequate facility elsewhere --CHILD--> [?] Person awaiting admission to mental health facility or unit --- Walk 4 --- [QB14] Unavailability or inaccessibility of health care facilities --EXCLUDES--> [?] Person awaiting admission to adequate facility elsewhere --PARENT--> [?] Factors related to medical facilities or other health care --- 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 --PARENT--> [?] Causes of healthcare related harm or injury
[ "[PL14.C] Patient received diagnostic test or treatment intended for another patient\n --EXCLUDES--> [?] Procedure undertaken at wrong site or wrong side, as mode of injury or harm\n --CHILD--> [?] Performance of inappropriate operation", "[PL14.C] Patient received diagnostic test or treatment intended for another patient\n --EXCLUDES--> [?] Procedure undertaken at wrong site or wrong side, as mode of injury or harm\n --EXCLUDES--> [?] Patient received diagnostic test or treatment intended for another patient", "[QB14] Unavailability or inaccessibility of health care facilities\n --EXCLUDES--> [?] Person awaiting admission to adequate facility elsewhere\n --CHILD--> [?] Person awaiting admission to mental health facility or unit", "[QB14] Unavailability or inaccessibility of health care facilities\n --EXCLUDES--> [?] Person awaiting admission to adequate facility elsewhere\n --PARENT--> [?] Factors related to medical facilities or other health care", "[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 --PARENT--> [?] Causes of healthcare related harm or injury" ]
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": "4A01.03", "icd10_code": "D807", "icd10_title": "Transient hypogammaglobulinemia of infancy" }, { "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" } ]
Z753
Unavailability and inaccessibility of health-care facilities
Extrahepatic bile duct resection is performed as part of radical cholecystectomy for gallbladder cancer. However, the indication for extrahepatic bile duct resection remains a major controversy in the surgical management of gallbladder cancer that has not invaded the hepatoduodenal ligament. The 2019 clinical practice guidelines for the management of biliary tract cancers advocated by the Japanese Society of Hepato-Biliary-Pancreatic Surgery recommend not to perform routine prophylactic extrahepatic bile duct resection for gallbladder cancer without bile duct invasion . Because of the patient’s age and activities of daily living, we considered that minimally invasive surgery was desirable. Moreover, preoperative imaging studies did not reveal evidence of extramural, cystic ductal, and bile ductal invasion, or evidence of regional lymph node metastasis. Therefore, extrahepatic bile duct resection was planned to be omitted in this case, although lymph node dissection around the hepatic portal region without extrahepatic bile duct resection may carry a risk of bile duct ischemia and can cause acute or chronic bile duct stenosis . Surgery with strict attention to conservation of blood flow to the bile duct was performed, then remnant cholecystectomy without extrahepatic bile duct resection was completed after confirmation of negative cystic ductal and surgical margins on intraoperative frozen section.
4.0625
0.826172
sec[2]/p[6]
en
0.999995
35187597
https://doi.org/10.1186/s40792-022-01388-8
[ "bile", "duct", "extrahepatic", "resection", "gallbladder", "cancer", "without", "ductal", "cholecystectomy", "that" ]
[ { "code": "DC10.2", "title": "Fistula of gallbladder or bile duct" }, { "code": "DC10.02", "title": "Obstruction of bile duct" }, { "code": "DC13", "title": "Cholangitis" }, { "code": "LB20.2Y", "title": "Other specified structural developmental anomalies of bile ducts" }, { "code": "ME24.35&XA6R80", "title": "Perforation of bile duct" }, { "code": "DC10.00", "title": "Obstruction of cystic duct" }, { "code": "LB20.23", "title": "Structural developmental anomalies of cystic duct" }, { "code": "LB20.21", "title": "Biliary atresia" }, { "code": "LA90.21", "title": "Congenital portosystemic shunt" }, { "code": "2E92.6", "title": "Benign neoplasm of gallbladder, extrahepatic bile ducts or ampulla of Vater" } ]
=== ICD-11 CODES FOUND === [DC10.2] Fistula of gallbladder or bile duct Definition: This is an abnormal connection or passageway between gallbladder or bile duct and other organs. Also known as: Fistula of gallbladder or bile duct | fistula of gallbladder | gallbladder fistula | Cholecystocolic fistula | Cholecystoduodenal fistula [DC10.02] Obstruction of bile duct Also known as: Obstruction of bile duct | extrahepatic biliary obstruction | extrahepatic bile duct obstruction | bile duct obstruction | bile stasis Excludes: with cholelithiasis [DC13] Cholangitis Also known as: Cholangitis | acute cholangiolitis | ascending cholangitis | cholangiolitis | cholangitis NOS Excludes: chronic nonsuppurative destructive cholangitis | cholangitis with cholelithiasis | Primary sclerosing cholangitis [LB20.2Y] Other specified structural developmental anomalies of bile ducts Also known as: Other specified structural developmental anomalies of bile ducts | Anomalous arrangement of pancreatobiliary ducts | Aberrant hepatic duct | Accessory hepatic duct | accessory liver duct [DC10.00] Obstruction of cystic duct Also known as: Obstruction of cystic duct | cystic duct obstruction | cystic ductal obstruction | obstructed cystic duct | Acquired cystic duct atresia [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 [LB20.21] Biliary atresia Definition: Biliary atresia is a rare disease characterised by an inflammatory biliary obstruction of unknown origin that presents in the neonatal period. It is the most frequent surgical cause of cholestatic jaundice in this age group. Untreated, this condition leads to cirrhosis and death within the first years of life. Also known as: Biliary atresia | Atresia of bile ducts | bile duct atresia | congenital bile duct atresia | congenital biliary atresia [LA90.21] Congenital portosystemic shunt Also known as: Congenital portosystemic shunt | anomalous pulmonary venous drainage to hepatic veins | anomaly of portal vein connection | portal vein deformity | portal vein anomaly [2E92.6] Benign neoplasm of gallbladder, extrahepatic bile ducts or ampulla of Vater Also known as: Benign neoplasm of gallbladder, extrahepatic bile ducts or ampulla of Vater | benign cholecystic neoplasm | Benign neoplasm of gallbladder and bile duct | Adenoma of bile ducts | adenoma of bile duct, unspecified site Includes: Adenoma of extrahepatic bile duct === GRAPH WALKS === --- Walk 1 --- [DC10.2] Fistula of gallbladder or bile duct Def: This is an abnormal connection or passageway between gallbladder or bile duct and other organs.... --PARENT--> [DC10] Acquired anatomical alterations of gallbladder or bile ducts Def: This considers the structure in the alterations of the gall bladder and the long tube-like structures that carry bile.... --CHILD--> [DC10.0] Obstruction of gallbladder or bile ducts Def: This is obstruction in the small organ that aids mainly in fat digestion and concentrates bile produced by the liver and in any of a number of long tube-like structures that carry bile.... --- Walk 2 --- [DC10.2] Fistula of gallbladder or bile duct Def: This is an abnormal connection or passageway between gallbladder or bile duct and other organs.... --PARENT--> [DC10] Acquired anatomical alterations of gallbladder or bile ducts Def: This considers the structure in the alterations of the gall bladder and the long tube-like structures that carry bile.... --CHILD--> [DC10.1] Hydrops of gallbladder Def: Abnormal accumulation of serous fluid in the gallbladder... --- Walk 3 --- [DC10.02] Obstruction of bile duct --EXCLUDES--> [?] Cholelithiasis Def: Cholelithiasis is calculus of gallbladder, cystic duct or bile duct. Most stones in the gallbladder are asymptomatic, but the most common initial symptom is biliary colic before the development of com... --CHILD--> [?] Calculus of gallbladder or cystic duct with other cholecystitis Def: Stones in gallbladder or cystic duct present with inflammation of the gall bladder wall and cystic duct.... --- Walk 4 --- [DC10.02] Obstruction of bile duct --EXCLUDES--> [?] Cholelithiasis Def: Cholelithiasis is calculus of gallbladder, cystic duct or bile duct. Most stones in the gallbladder are asymptomatic, but the most common initial symptom is biliary colic before the development of com... --CHILD--> [?] Calculus of gallbladder or cystic duct with acute cholecystitis Def: Stones in gallbladder or cystic duct present with acute inflammation of the gall bladder wall typically follows the cystic duct obstruction by the stone.... --- Walk 5 --- [DC13] Cholangitis --EXCLUDES--> [?] Calculus of bile duct with cholangitis Def: Stones in bile duct present with inflammation of bile duct.... --CHILD--> [?] Calculus of bile duct with other cholangitis Def: This is an infection of the bile duct (cholangitis), usually caused by bacteria ascending from its junction with the duodenum (first part of the small intestine).... --- Walk 6 --- [DC13] Cholangitis --EXCLUDES--> [?] Primary biliary cholangitis Def: Primary biliary cholangitis is characterised by progressive destruction and disappearance of the intralobular bile duct epithelial cells leading to cholestasis (high alkaline phosphatase and GGT {gamm... --EXCLUDES--> [?] Hepatic fibrosis or cirrhosis
[ "[DC10.2] Fistula of gallbladder or bile duct\n Def: This is an abnormal connection or passageway between gallbladder or bile duct and other organs....\n --PARENT--> [DC10] Acquired anatomical alterations of gallbladder or bile ducts\n Def: This considers the structure in the alterations of the gall bladder and the long tube-like structures that carry bile....\n --CHILD--> [DC10.0] Obstruction of gallbladder or bile ducts\n Def: This is obstruction in the small organ that aids mainly in fat digestion and concentrates bile produced by the liver and in any of a number of long tube-like structures that carry bile....", "[DC10.2] Fistula of gallbladder or bile duct\n Def: This is an abnormal connection or passageway between gallbladder or bile duct and other organs....\n --PARENT--> [DC10] Acquired anatomical alterations of gallbladder or bile ducts\n Def: This considers the structure in the alterations of the gall bladder and the long tube-like structures that carry bile....\n --CHILD--> [DC10.1] Hydrops of gallbladder\n Def: Abnormal accumulation of serous fluid in the gallbladder...", "[DC10.02] Obstruction of bile duct\n --EXCLUDES--> [?] Cholelithiasis\n Def: Cholelithiasis is calculus of gallbladder, cystic duct or bile duct. Most stones in the gallbladder are asymptomatic, but the most common initial symptom is biliary colic before the development of com...\n --CHILD--> [?] Calculus of gallbladder or cystic duct with other cholecystitis\n Def: Stones in gallbladder or cystic duct present with inflammation of the gall bladder wall and cystic duct....", "[DC10.02] Obstruction of bile duct\n --EXCLUDES--> [?] Cholelithiasis\n Def: Cholelithiasis is calculus of gallbladder, cystic duct or bile duct. Most stones in the gallbladder are asymptomatic, but the most common initial symptom is biliary colic before the development of com...\n --CHILD--> [?] Calculus of gallbladder or cystic duct with acute cholecystitis\n Def: Stones in gallbladder or cystic duct present with acute inflammation of the gall bladder wall typically follows the cystic duct obstruction by the stone....", "[DC13] Cholangitis\n --EXCLUDES--> [?] Calculus of bile duct with cholangitis\n Def: Stones in bile duct present with inflammation of bile duct....\n --CHILD--> [?] Calculus of bile duct with other cholangitis\n Def: This is an infection of the bile duct (cholangitis), usually caused by bacteria ascending from its junction with the duodenum (first part of the small intestine)....", "[DC13] Cholangitis\n --EXCLUDES--> [?] Primary biliary cholangitis\n Def: Primary biliary cholangitis is characterised by progressive destruction and disappearance of the intralobular bile duct epithelial cells leading to cholestasis (high alkaline phosphatase and GGT {gamm...\n --EXCLUDES--> [?] Hepatic fibrosis or cirrhosis" ]
DC10.2
Fistula of gallbladder or bile duct
[ { "from_icd11": "DC10.2", "icd10_code": "K833", "icd10_title": "Fistula of bile duct" }, { "from_icd11": "DC10.2", "icd10_code": "K823", "icd10_title": "Fistula of gallbladder" }, { "from_icd11": "DC10.02", "icd10_code": "K831", "icd10_title": "Obstruction of bile duct" }, { "from_icd11": "DC13", "icd10_code": "K8309", "icd10_title": "Other cholangitis" }, { "from_icd11": "DC13", "icd10_code": "K8301", "icd10_title": "Primary sclerosing cholangitis" }, { "from_icd11": "DC13", "icd10_code": "K830", "icd10_title": "Cholangitis" }, { "from_icd11": "LB20.21", "icd10_code": "Q442", "icd10_title": "Atresia of bile ducts" }, { "from_icd11": "LA90.21", "icd10_code": "Q265", "icd10_title": "Anomalous portal venous connection" }, { "from_icd11": "2E92.6", "icd10_code": "D135", "icd10_title": "Benign neoplasm of extrahepatic bile ducts" } ]
K833
Fistula of bile duct
A 15-year-old male patient presented to the trauma emergency room intubated in the field with multiple gunshot wounds. On the primary survey, the patient was tachycardic and intubated. The patient's heart rate ranged from 100 to 120 bpm, sinus tachycardia, and blood pressure 100/60 mm Hg. In the secondary survey, the patient had multiple gunshot wounds to the chest, abdomen, bilateral lower limbs, and left upper extremity. The patient had palpable pulses in the bilateral lower extremity and left upper extremity. In the trauma emergency room, the patient had left tube thoracostomy for a left hemothorax performed bedside. The patient underwent computed tomography imaging suggestive of pneumoperitoneum, an X-ray and angiogram of left upper extremity suggestive of left upper extremity comminuted humerus fracture and left upper limb ulnar artery injury . The patient underwent damage control exploratory laparotomy. Diaphragmatic injury and bladder injuries were repaired primarily, small and large bowel left in discontinuity, and for pelvic wall bleeding, preperitoneal packing was performed. Abdomen fascia was left open with temporary closure performed using the wound VAC (vacuum-assisted device). For left humerus fracture with an expanding hematoma fasciotomy of the left upper limb was performed. On completion of the left upper limb's fasciotomy, there were no radial or ulnar pulses for Doppler signals.
3.650391
0.985352
sec[1]/p[0]
en
0.999998
32789087
https://doi.org/10.7759/cureus.9150
[ "extremity", "limb", "trauma", "emergency", "room", "intubated", "multiple", "gunshot", "wounds", "survey" ]
[ { "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": "ND56.Z", "title": "Unspecified injury to unspecified part of trunk, limb or body region" }, { "code": "ND37", "title": "Unspecified multiple injuries" }, { "code": "NB91.Y&XA9607", "title": "Injury of intestine" }, { "code": "ND56.4", "title": "Injury of nerve of unspecified body region" }, { "code": "NF0A.Z", "title": "Early complications of trauma, not elsewhere classified" } ]
=== 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 [ND56.Z] Unspecified injury to unspecified part of trunk, limb or body region Also known as: Unspecified injury to unspecified part of trunk, limb or body region | Injury of unspecified body region | injury NOS | trauma NOS | traumatic injury NOS [ND37] Unspecified multiple injuries Also known as: Unspecified multiple injuries | multiple trauma NOS | multiple traumatic injuries | multiple sites of injury | multiple system injury Excludes: injury NOS [ND56.4] Injury of nerve of unspecified body region Also known as: Injury of nerve of unspecified body region | injuries to nerves, nerve plexuses and roots | injury to nerves, unspecified site | nerve damage NOS | Injury of nerve NOS Excludes: multiple injuries of nerves NOS [NF0A.Z] Early complications of trauma, not elsewhere classified Also known as: Early complications of trauma, not elsewhere classified | Certain early complications of trauma, not elsewhere classified | early trauma complications | early complication of trauma | trauma complications === GRAPH WALKS === --- Walk 1 --- [ND56.1] Open wound of unspecified body region --EXCLUDES--> [?] Traumatic amputations involving multiple body regions --EXCLUDES--> [?] Other injuries of leg, level unspecified --- Walk 2 --- [ND56.1] Open wound of unspecified body region --EXCLUDES--> [?] Traumatic amputation of unspecified body region --CHILD--> [?] Sequelae of traumatic amputation of unspecified body region --- 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--> [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 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.... --PARENT--> [?] Structural developmental anomalies primarily affecting one body system Def: A deformation established before birth of an anatomical structure.... --- 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--> [FB56.2] Myalgia Def: This is a disorder characterised by pain in a muscle or group of muscles.... --- 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.... --EXCLUDES--> [?] Mononeuropathy
[ "[ND56.1] Open wound of unspecified body region\n --EXCLUDES--> [?] Traumatic amputations involving multiple body regions\n --EXCLUDES--> [?] Other injuries of leg, level unspecified", "[ND56.1] Open wound of unspecified body region\n --EXCLUDES--> [?] Traumatic amputation of unspecified body region\n --CHILD--> [?] Sequelae of traumatic amputation of unspecified body region", "[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....", "[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 --PARENT--> [?] Structural developmental anomalies primarily affecting one body system\n Def: A deformation established before birth of an anatomical structure....", "[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--> [FB56.2] Myalgia\n Def: This is a disorder characterised by pain in a muscle or group of muscles....", "[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--> [?] Mononeuropathy" ]
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
Case 1 was a 77-year-old woman who underwent total hip arthroplasty (THA) for femoral neck fracture 5 years ago. Her hip pain had worsened for about 2 weeks, and she was admitted with a C-reactive protein (CRP) of 7. 38 mg/L and an erythrocyte sedimentation rate (ESR) of 36 mm/h. A synovial fluid aspiration and test was performed preoperatively, the synovial fluid white blood cell (SF-WBC) was 56367×10 6 /L and the synovial fluid polymorphonuclear neutrophils (SF-PMN) percentage was 89.9%. To better identify the pathogenic organisms, routine microbial culture and mNGS were both performed preoperatively. About 48 hours later, the mNGS results indicated that it was a multiple infection caused by Staphylococcus epidermidis ( S. epidermidis ) and Mycoplasma hyorhinis , while microbial culture and 16S PCR only showed the potential infection by S. epidermidis . Unfortunately, CRP and ESR remained at high levels and the infection could not be controlled after microbial culture results oriented antibiotics treatment. Based on symptoms, physical examination and medical history, the PJI panel reconsidered that the Mycoplasma hyorhinis was also the true pathogen rather than background bacteria. Therefore, a two-stage revision was performed and a modified antibiotic regimen (levofloxacin + doxycycline) was adopted, and finally the inflammatory indexes decreased to normal and the infection was well controlled.
3.992188
0.981445
sec[2]/sec[3]/p[0]
en
0.999997
PMC10014592
https://doi.org/10.3389/fcimb.2023.1089919
[ "infection", "synovial", "fluid", "microbial", "culture", "epidermidis", "about", "preoperatively", "mngs", "that" ]
[ { "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" }, { "code": "FB41.1", "title": "Spontaneous rupture of synovium" }, { "code": "MG6Y", "title": "Other specified clinical findings in specimens from other specified organs, systems and tissues" }, { "code": "FB42.3", "title": "Synovial hypertrophy, not elsewhere classified" }, { "code": "FB50.Y", "title": "Other specified bursitis" }, { "code": "EK70.2", "title": "Digital myxoid pseudocyst" } ]
=== ICD-11 CODES FOUND === [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] [FB41.1] Spontaneous rupture of synovium Definition: This is a rupture to a fluid-filled sac containing viscous fluid which normally acts to decrease friction and also provides a cushion between bones and tendons and/or muscles around a joint. Also known as: Spontaneous rupture of synovium | rupture of synovium, site unspecified | synovial rupture | Rupture of synovium | Spontaneous rupture of synovium, multiple sites Excludes: Spontaneous rupture of popliteal cyst [MG6Y] Other specified clinical findings in specimens from other specified organs, systems and tissues Also known as: Other specified clinical findings in specimens from other specified organs, systems and tissues | Abnormal amniotic fluid | Abnormal findings in nipple discharge | Abnormal findings in synovial fluid | abnormal synovial fluid [FB42.3] Synovial hypertrophy, not elsewhere classified Definition: This is an increase in synovial lining thickness which is not elsewhere classified. Also known as: Synovial hypertrophy, not elsewhere classified [FB50.Y] Other specified bursitis Also known as: Other specified bursitis | Synovial cyst, not elsewhere classified | synovial cyst NOS | Adhesive bursitis | Bursopathy, not elsewhere classified [EK70.2] Digital myxoid pseudocyst Definition: Digital myxoid cysts (DMCs) are benign ganglion cysts of the digits, which typically present as a small dome-shaped, often translucent papule on the dorsum of the terminal phalanx and/or as longitudinal "guttering" of the nail plate which is focally compressed by the cyst as it develops from the underlying nail matrix. In the majority of cases a stalk connecting the cyst with the adjacent distal interphalangeal joint can be demonstrated, accounting for the alternative names of digital ganglion c Also known as: Digital myxoid pseudocyst | Digital ganglion cyst | Digital mucous cyst | Synovial cyst of digit | Digital synovial cyst Includes: Digital ganglion cyst === GRAPH WALKS === --- Walk 1 --- [1H0Z] Infection, unspecified --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.... --RELATED_TO--> [?] Human prion diseases Def: Human prion diseases or transmissible spongiform encephalopathies are rare transmissible diseases affecting the central nervous system. The infectious agents are composed of an abnormal isoform of a h... --- Walk 2 --- [1H0Z] Infection, unspecified --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.... --EXCLUDES--> [?] Infection arising from device, implant or graft, not elsewhere classified --- Walk 3 --- [1G40] Sepsis without septic shock Def: Sepsis is defined as a life-threatening organ dysfunction caused by a dysregulated host response to infection.... --PARENT--> [?] Sepsis --RELATED_TO--> [?] Puerperal sepsis --- Walk 4 --- [1G40] Sepsis without septic shock Def: Sepsis is defined as a life-threatening organ dysfunction caused by a dysregulated host response to infection.... --EXCLUDES--> [?] Sepsis of fetus or newborn --EXCLUDES--> [?] Sepsis with septic shock Def: Septic shock is a subset of sepsis in which circulatory, cellular and metabolic abnormalities are profound enough to substantially increase mortality.... --- Walk 5 --- [FA10.Z] Direct infections of joint, unspecified --PARENT--> [FA10] Direct infections of joint Def: Hematogenic or non-hematogenic infections of joints.... --CHILD--> [FA10.0] Bacterial 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--> [?] Postinfectious arthropathies
[ "[1H0Z] Infection, unspecified\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....\n --RELATED_TO--> [?] Human prion diseases\n Def: Human prion diseases or transmissible spongiform encephalopathies are rare transmissible diseases affecting the central nervous system. The infectious agents are composed of an abnormal isoform of a h...", "[1H0Z] Infection, unspecified\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....\n --EXCLUDES--> [?] Infection arising from device, implant or graft, not elsewhere classified", "[1G40] Sepsis without septic shock\n Def: Sepsis is defined as a life-threatening organ dysfunction caused by a dysregulated host response to infection....\n --PARENT--> [?] Sepsis\n --RELATED_TO--> [?] Puerperal sepsis", "[1G40] Sepsis without septic shock\n Def: Sepsis is defined as a life-threatening organ dysfunction caused by a dysregulated host response to infection....\n --EXCLUDES--> [?] Sepsis of fetus or newborn\n --EXCLUDES--> [?] Sepsis with septic shock\n Def: Septic shock is a subset of sepsis in which circulatory, cellular and metabolic abnormalities are profound enough to substantially increase mortality....", "[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--> [FA10.0] Bacterial 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--> [?] Postinfectious arthropathies" ]
1H0Z
Infection, unspecified
[ { "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" }, { "from_icd11": "1H0Z", "icd10_code": "I", "icd10_title": "" }, { "from_icd11": "1H0Z", "icd10_code": "B90-B94", "icd10_title": "" }, { "from_icd11": "1H0Z", "icd10_code": "B94", "icd10_title": "Sequelae of other and unspecified infectious and parasitic diseases" } ]
B999
Unspecified infectious disease
This case report presents the diagnostic difficulties associated with the diagnosis of RMS syndrome. This description presents a patient with the presence of two causative variants in the INSR gene and typical phenotypic features of RMS, but without short stature and with normal IGF-1 levels. To date, only isolated cases of RMS have been described in which, at least at some stage of postnatal life, body height was within normal limits (without IGF-1 therapy) . Low IGF-1 levels therefore seem to be commonly observed in patients with RMS/DS . Only Dutta et al. described a girl suspected of having RMS (the diagnosis was made on the basis of clinical presentation without genetic testing), whose IGF-1 was in the lower limits of normal . The exact cause of impaired growth hormone (GH) secretion in RMS is not clear. Since insulin signalling is impaired in RMS, it appears that insulin in high concentrations may inhibit GH secretion through cross-talk signalling via the IGF-I receptor. There is also evidence to suggest that insulin increases hepatic IGF-1 and IGFBP-3 production through direct regulation of the GH receptor, and thus, in patients with severe insulin resistance, IGF-1 deficiency may be due to both impaired hepatic production and accelerated IGF-I excretion . Individuals with RMS are therefore typically small relative to gestational age and exhibit postnatal short stature of varying severity .
4.328125
0.87793
sec[3]/p[0]
en
0.999995
36331627
https://doi.org/10.1007/s00592-022-01971-3
[ "insulin", "without", "impaired", "this", "presents", "short", "stature", "postnatal", "limits", "therefore" ]
[ { "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": "MH12.1", "title": "Death occurring less than 24 hours from onset of symptoms, not otherwise explained" }, { "code": "FA36.Y", "title": "Other specified effusion of joint" }, { "code": "3A51.1", "title": "Sickle cell disease without crisis" }, { "code": "QA50", "title": "Embolisation without injury or harm" }, { "code": "LB12.1Z", "title": "Atresia of oesophagus, unspecified" } ]
=== 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 [MH12.1] Death occurring less than 24 hours from onset of symptoms, not otherwise explained Also known as: Death occurring less than 24 hours from onset of symptoms, not otherwise explained | died without sign of disease | Death known not to be violent or instantaneous for which no cause can be discovered | death known not to be violent or instantaneous, cause unknown | Death without sign of disease Includes: Death known not to be violent or instantaneous for which no cause can be discovered | Death without sign of disease [FA36.Y] Other specified effusion of joint Also known as: Other specified effusion of joint | Non aspirated effusion of joint | Effusion of joint without blood | Effusion of joint, multiple sites | Effusion of joint, shoulder region [3A51.1] Sickle cell disease without crisis Definition: A disorder caused by a HbS mutation in the haemoglobin gene. This disorder is characterised by abnormal rigid sickle-shaped red blood cells decreasing its ability to carry oxygen. This disorder may present with fatigue, shortness of breath, dizziness, headaches, pallor of skin or mucous membranes, and jaundice. This disorder is confirmed by identification of HbS mutation by genetic testing. Also known as: Sickle cell disease without crisis | Hb-SS disease without crisis | HbSS without crisis | Sickle-cell anaemia without crisis | SCD - [sickle cell disease] [QA50] Embolisation without injury or harm Definition: An embolisation without documented injury or harm occurs when a solid object within the venous or arterial circulation propagates to a distal location and becomes lodged there. Also known as: Embolisation without injury or harm | Embolic phenomenon without documented injury or harm | Air embolism without documented injury or harm | Injection of air without injury or harm Excludes: Embolisation, as mode of injury or harm [LB12.1Z] Atresia of oesophagus, unspecified Also known as: Atresia of oesophagus, unspecified | Atresia of oesophagus | atresia of esophagus | Atresia of oesophagus without fistula | congenital atresia of oesophagus === 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--> [?] Malignant neoplasm of pancreas Def: A primary malignant tumour of the pancreas. Most are adenocarcinomas.... --- Walk 5 --- [QB51.5] Presence of endocrine implants --PARENT--> [QB51] Presence of devices other than cardiac or vascular implants --EXCLUDES--> [?] Fitting, adjustment or management of devices --- Walk 6 --- [QB51.5] Presence of endocrine implants --PARENT--> [QB51] Presence of devices other than cardiac or vascular implants --CHILD--> [QB51.2] Presence of intraocular lens
[ "[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--> [?] Malignant neoplasm of pancreas\n Def: A primary malignant tumour of the pancreas. Most are adenocarcinomas....", "[QB51.5] Presence of endocrine implants\n --PARENT--> [QB51] Presence of devices other than cardiac or vascular implants\n --EXCLUDES--> [?] Fitting, adjustment or management of devices", "[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" ]
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
We present the case of a 65-year-old woman diagnosed with FD and severe organ involvement treated with migalastat for the last 3 years. The patient had a long medical history, including multiple conditions such as cardiac hypertrophy with preserved left ventricular ejection fraction (LVEF) and diastolic dysfunction, exertional dyspnoea, cutaneous lupus disease, primary antiphospholipid syndrome, dyslipidaemia, hypertension, and atrophic gastritis. She is currently being treated with torasemide, amiodarone, enalapril, bisoprolol, acenocoumarol, and pravastatin. In 2016, she suffered a stroke of the right middle cerebral artery along with paroxysmal atrial fibrillation. At that time, typical FD manifestations (severe sensorineural hypoacusis, cornea verticillata, and angiokeratomas) were also detected . Genetic testing demonstrated the presence of a pathogenic sequence variant in the GLA gene: c.809T >C p.(Ile270Thr), the same as the previous case although not a relative . Plasma α ‐Gal A activity was decreased (less than 30%) ( Figure 4(a) ). Cardiac hypertrophy was then attributed to FD. Fabry-specific therapy was immediately initiated with enzyme replacement therapy (ERT) (agalsidase beta) . Regarding her family history, although her mother had a hypertrophic cardiomyopathy and her father and brother had ischaemic heart disease and sensorineural hearing loss, genetic testing was negative for FD .
4.050781
0.979492
sec[1]/sec[1]/p[0]
en
0.999996
PMC9822754
https://doi.org/10.1155/2022/3208810
[ "treated", "cardiac", "hypertrophy", "sensorineural", "genetic", "testing", "although", "present", "diagnosed", "organ" ]
[ { "code": "BE2Y", "title": "Other specified diseases of the circulatory system" }, { "code": "BC4Z", "title": "Diseases of the myocardium or cardiac chambers, unspecified" }, { "code": "BD1Z", "title": "Heart failure, unspecified" }, { "code": "LA8Z", "title": "Structural developmental anomaly of heart or great vessels, unspecified" }, { "code": "BA41.Z", "title": "Acute myocardial infarction, unspecified" }, { "code": "FB32.Y", "title": "Other specified disorders of muscles" }, { "code": "FB86.11", "title": "Hypertrophy of bone" }, { "code": "MA01.Z", "title": "Enlarged lymph nodes, unspecified" }, { "code": "FB4Y", "title": "Other specified disorders of synovium or tendon" }, { "code": "FA34.1", "title": "Disorder of ligament" } ]
=== 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 [BC4Z] Diseases of the myocardium or cardiac chambers, unspecified Also known as: Diseases of the myocardium or cardiac chambers, unspecified | Heart disease NOS | cardiac disease NOS [BD1Z] Heart failure, unspecified Also known as: Heart failure, unspecified | myocardial failure | cardiac decompensation | cardiac failure | cardiac failure NOS [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 [BA41.Z] Acute myocardial infarction, unspecified Also known as: Acute myocardial infarction, unspecified | Acute myocardial infarction | cardiac attack | heart attack | acute cardiac infarction [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 [FB86.11] Hypertrophy of bone Also known as: Hypertrophy of bone | bone thickening | periosteum thickening | Infantile cortical hyperostoses | Post traumatic subperiosteal ossification [MA01.Z] Enlarged lymph nodes, unspecified Also known as: Enlarged lymph nodes, unspecified | Enlarged lymph nodes | swollen glands | Lymphadenopathy | adenopathy [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 [FA34.1] Disorder of ligament Also known as: Disorder of ligament | disorder of ligament, unspecified site | ligament disorder | disease of ligament | ligament deformity Excludes: Chronic instability of knee | familial ligamentous laxity === 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... --RELATED_TO--> [?] Cerebrovascular diseases Def: This is a group of brain dysfunctions related to disease of the blood vessels supplying the brain. This includes “stroke”, which includes the following entities: Intracerebral haemorrhage; Subarachnoi... --- 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... --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 --- [BC4Z] Diseases of the myocardium or cardiac chambers, unspecified --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 4 --- [BC4Z] Diseases of the myocardium or cardiac chambers, unspecified --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 5 --- [BD1Z] Heart failure, unspecified --PARENT--> [?] Heart failure --CHILD--> [BD10] Congestive heart failure Def: A clinical syndrome characterised by abnormalities of ventricular function and neurohormonal regulation which are accompanied by effort intolerance and fluid retention.... --- Walk 6 --- [BD1Z] Heart failure, unspecified --PARENT--> [?] Heart failure --EXCLUDES--> [?] Other complications of obstetric surgery or procedures Def: Any complication caused by or subsequent to obstetric surgery and procedures, and not elsewhere classified....
[ "[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 --RELATED_TO--> [?] Cerebrovascular diseases\n Def: This is a group of brain dysfunctions related to disease of the blood vessels supplying the brain. This includes “stroke”, which includes the following entities: Intracerebral haemorrhage; Subarachnoi...", "[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 --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....", "[BC4Z] Diseases of the myocardium or cardiac chambers, unspecified\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...", "[BC4Z] Diseases of the myocardium or cardiac chambers, unspecified\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...", "[BD1Z] Heart failure, unspecified\n --PARENT--> [?] Heart failure\n --CHILD--> [BD10] Congestive heart failure\n Def: A clinical syndrome characterised by abnormalities of ventricular function and neurohormonal regulation which are accompanied by effort intolerance and fluid retention....", "[BD1Z] Heart failure, unspecified\n --PARENT--> [?] Heart failure\n --EXCLUDES--> [?] Other complications of obstetric surgery or procedures\n Def: Any complication caused by or subsequent to obstetric surgery and procedures, and not elsewhere classified...." ]
BE2Y
Other specified diseases of the circulatory system
[ { "from_icd11": "BC4Z", "icd10_code": "I5181", "icd10_title": "Takotsubo syndrome" }, { "from_icd11": "BC4Z", "icd10_code": "I5189", "icd10_title": "Other ill-defined heart diseases" }, { "from_icd11": "BC4Z", "icd10_code": "I519", "icd10_title": "Heart disease, unspecified" }, { "from_icd11": "BC4Z", "icd10_code": "I510", "icd10_title": "Cardiac septal defect, acquired" }, { "from_icd11": "BC4Z", "icd10_code": "I515", "icd10_title": "Myocardial degeneration" }, { "from_icd11": "BC4Z", "icd10_code": "I51", "icd10_title": "Complications and ill-defined descriptions of heart disease" }, { "from_icd11": "BC4Z", "icd10_code": "I516", "icd10_title": "" }, { "from_icd11": "BC4Z", "icd10_code": "I518", "icd10_title": "Other ill-defined heart diseases" }, { "from_icd11": "BD1Z", "icd10_code": "I5023", "icd10_title": "Acute on chronic systolic (congestive) heart failure" }, { "from_icd11": "BD1Z", "icd10_code": "I5030", "icd10_title": "Unspecified diastolic (congestive) heart failure" }, { "from_icd11": "BD1Z", "icd10_code": "I5031", "icd10_title": "Acute diastolic (congestive) heart failure" }, { "from_icd11": "BD1Z", "icd10_code": "I5022", "icd10_title": "Chronic systolic (congestive) heart failure" }, { "from_icd11": "BD1Z", "icd10_code": "I5084", "icd10_title": "End stage heart failure" }, { "from_icd11": "BD1Z", "icd10_code": "I5020", "icd10_title": "Unspecified systolic (congestive) heart failure" }, { "from_icd11": "BD1Z", "icd10_code": "I5021", "icd10_title": "Acute systolic (congestive) heart failure" } ]
I5181
Takotsubo syndrome
Malignant hypertension is defined as uncontrolled severe hypertension in the presence of acute organ damage including the brain, heart, and kidney. This condition is often associated with thrombotic microangiopathy, which is an expression of endothelial acute damage ( 9 ). For this reason, it has to be differentiated from thrombotic thrombocytopenic purpura, which addresses the management of the case toward plasma exchange. Bosisio et al. describe the case of a patient affected by malignant hypertension. Prior history of hypertension, high mean arterial pressure, significant renal impairment but relatively modest thrombocytopenia, and a lack of severe ADAMTS-13 deficiency (activity <10%) at diagnosis are clues to diagnose malignant hypertension-induced thrombotic microangiopathy Bosisio et al . This very well-described case allows the reader to focus on three major issues: (1) Malignant hypertension needs to be included in the flowchart for the diagnosis in the presence of acute syndrome in order to save time and prevent further damage; (2) fast reduction of blood pressure levels might as well favor the progression of the organ damage, given the reduced perfusion of target organs such as the heart or the kidney; (3) recidivism occurs, in particular, to those patients who do not adhere to treatment; therefore, strategies for improving adherence (including closer follow-ups) need to be put in place.
4.144531
0.814941
sec[6]/p[0]
en
0.999996
PMC10241069
https://doi.org/10.3389/fcvm.2023.1210740
[ "hypertension", "malignant", "damage", "this", "thrombotic", "presence", "organ", "including", "heart", "kidney" ]
[ { "code": "BA00.Z", "title": "Essential hypertension, unspecified" }, { "code": "9C61.01", "title": "Ocular hypertension" }, { "code": "BB01.Z", "title": "Pulmonary hypertension, unspecified" }, { "code": "JA23", "title": "Gestational hypertension" }, { "code": "BA04.Y", "title": "Other specified secondary hypertension" }, { "code": "2D4Z", "title": "Unspecified malignant neoplasms of unspecified sites" }, { "code": "2E2Z", "title": "Malignant neoplasm metastasis, unspecified" }, { "code": "2B70.Z", "title": "Malignant neoplasms of oesophagus, unspecified" }, { "code": "2B33.Y", "title": "Other malignant haematopoietic neoplasms without further specification" }, { "code": "2B31.1", "title": "Histiocytic sarcoma" } ]
=== ICD-11 CODES FOUND === [BA00.Z] Essential hypertension, unspecified Also known as: Essential hypertension, unspecified | Essential hypertension | idiopathic hypertension | primary hypertension | systemic primary arterial hypertension [9C61.01] Ocular hypertension Definition: Ocular hypertension is a condition of elevated intraocular pressure in the absence of optic nerve, nerve fibre layer or visual field abnormalities. Also known as: Ocular hypertension | intraocular pressure increase | OH - [ocular hypertension] | OHT - [ocular hypertension] | ocular HTN - [hypertension] [BB01.Z] Pulmonary hypertension, unspecified Also known as: Pulmonary hypertension, unspecified | Pulmonary hypertension | pulmonary HTN - [hypertension] | Postcapillary pulmonary hypertension | Precapillary pulmonary hypertension [JA23] Gestational hypertension Definition: A condition affecting pregnant females, characterised by systolic blood pressure greater than 140mmHg and/or a diastolic blood pressure greater or equal to 90mmHg on two occasions, 4 hours or more apart. Can be newly diagnosed after 20 weeks gestation or before 1 week postpartum. Confirmation is by measurement of blood pressure, liver and kidney functions test, and urine test. Also known as: Gestational hypertension | gestational [pregnancy-induced] hypertension without significant proteinuria | Gestational hypertension NOS | hypertension induced by pregnancy | mild proteinuric hypertension of pregnancy [BA04.Y] Other specified secondary hypertension Also known as: Other specified secondary hypertension | Secondary hypertension associated with renal parenchymal disease | Secondary hypertension associated with renovascular disease | hypertension due to renovascular disease | renal vascular hypertension [2D4Z] Unspecified malignant neoplasms of unspecified sites Also known as: Unspecified malignant neoplasms of unspecified sites | malignancy of unspecified site | malignancy unspecified primary site | malignant growth of unspecified site | malignant mass of unspecified site [2E2Z] Malignant neoplasm metastasis, unspecified Also known as: Malignant neoplasm metastasis, unspecified | secondary malignant neoplasm | metastasis | metastases | disseminated metastases [2B70.Z] Malignant neoplasms of oesophagus, unspecified Also known as: Malignant neoplasms of oesophagus, unspecified | Malignant neoplasms of oesophagus | cancer of oesophagus | oesophageal malignancy | oesophageal cancer [2B33.Y] Other malignant haematopoietic neoplasms without further specification Also known as: Other malignant haematopoietic neoplasms without further specification | Malignant neoplasm blood other | Haematological malignancy NOS | Neoplasm blood benign or unspecified [2B31.1] Histiocytic sarcoma Also known as: Histiocytic sarcoma | Malignant Histiocytosis Includes: Malignant Histiocytosis === GRAPH WALKS === --- Walk 1 --- [BA00.Z] Essential hypertension, unspecified --PARENT--> [BA00] Essential hypertension Def: Essential (primary) hypertension, accounting for 95% of all cases of hypertension, is defined as high blood pressure for which a secondary cause cannot be found.... --CHILD--> [BA00.0] Combined diastolic and systolic hypertension --- Walk 2 --- [BA00.Z] Essential hypertension, unspecified --PARENT--> [BA00] Essential hypertension Def: Essential (primary) hypertension, accounting for 95% of all cases of hypertension, is defined as high blood pressure for which a secondary cause cannot be found.... --EXCLUDES--> [?] Cerebrovascular diseases Def: This is a group of brain dysfunctions related to disease of the blood vessels supplying the brain. This includes “stroke”, which includes the following entities: Intracerebral haemorrhage; Subarachnoi... --- Walk 3 --- [9C61.01] Ocular hypertension Def: Ocular hypertension is a condition of elevated intraocular pressure in the absence of optic nerve, nerve fibre layer or visual field abnormalities.... --PARENT--> [9C61.0] Primary open-angle glaucoma Def: Primary open-angle glaucoma is a chronic progressive optic neuropathy with characteristic morphological changes at the optic nerve head and retinal nerve fibre layer in the absence of other ocular dis... --CHILD--> [9C61.00] Normal tension glaucoma Def: Normal tension glaucoma is a condition considered to be within the continuum of primary open-angle glaucoma; the term is used when intraocular pressure is within the statistically normal range (10-21 ... --- Walk 4 --- [9C61.01] Ocular hypertension Def: Ocular hypertension is a condition of elevated intraocular pressure in the absence of optic nerve, nerve fibre layer or visual field abnormalities.... --PARENT--> [9C61.0] Primary open-angle glaucoma Def: Primary open-angle glaucoma is a chronic progressive optic neuropathy with characteristic morphological changes at the optic nerve head and retinal nerve fibre layer in the absence of other ocular dis... --CHILD--> [9C61.00] Normal tension glaucoma Def: Normal tension glaucoma is a condition considered to be within the continuum of primary open-angle glaucoma; the term is used when intraocular pressure is within the statistically normal range (10-21 ... --- Walk 5 --- [BB01.Z] Pulmonary hypertension, unspecified --PARENT--> [BB01] Pulmonary hypertension Def: Pulmonary hypertension (PH) is a haemodynamic and pathophysiological condition defined as an increase in mean pulmonary arterial pressure (PAP) 25 mmHg at rest as assessed by right heart catheterizati... --CHILD--> [BB01.1] Pulmonary hypertension due to left heart disease --- Walk 6 --- [BB01.Z] Pulmonary hypertension, unspecified --PARENT--> [BB01] Pulmonary hypertension Def: Pulmonary hypertension (PH) is a haemodynamic and pathophysiological condition defined as an increase in mean pulmonary arterial pressure (PAP) 25 mmHg at rest as assessed by right heart catheterizati... --CHILD--> [BB01.1] Pulmonary hypertension due to left heart disease
[ "[BA00.Z] Essential hypertension, unspecified\n --PARENT--> [BA00] Essential hypertension\n Def: Essential (primary) hypertension, accounting for 95% of all cases of hypertension, is defined as high blood pressure for which a secondary cause cannot be found....\n --CHILD--> [BA00.0] Combined diastolic and systolic hypertension", "[BA00.Z] Essential hypertension, unspecified\n --PARENT--> [BA00] Essential hypertension\n Def: Essential (primary) hypertension, accounting for 95% of all cases of hypertension, is defined as high blood pressure for which a secondary cause cannot be found....\n --EXCLUDES--> [?] Cerebrovascular diseases\n Def: This is a group of brain dysfunctions related to disease of the blood vessels supplying the brain. This includes “stroke”, which includes the following entities: Intracerebral haemorrhage; Subarachnoi...", "[9C61.01] Ocular hypertension\n Def: Ocular hypertension is a condition of elevated intraocular pressure in the absence of optic nerve, nerve fibre layer or visual field abnormalities....\n --PARENT--> [9C61.0] Primary open-angle glaucoma\n Def: Primary open-angle glaucoma is a chronic progressive optic neuropathy with characteristic morphological changes at the optic nerve head and retinal nerve fibre layer in the absence of other ocular dis...\n --CHILD--> [9C61.00] Normal tension glaucoma\n Def: Normal tension glaucoma is a condition considered to be within the continuum of primary open-angle glaucoma; the term is used when intraocular pressure is within the statistically normal range (10-21 ...", "[9C61.01] Ocular hypertension\n Def: Ocular hypertension is a condition of elevated intraocular pressure in the absence of optic nerve, nerve fibre layer or visual field abnormalities....\n --PARENT--> [9C61.0] Primary open-angle glaucoma\n Def: Primary open-angle glaucoma is a chronic progressive optic neuropathy with characteristic morphological changes at the optic nerve head and retinal nerve fibre layer in the absence of other ocular dis...\n --CHILD--> [9C61.00] Normal tension glaucoma\n Def: Normal tension glaucoma is a condition considered to be within the continuum of primary open-angle glaucoma; the term is used when intraocular pressure is within the statistically normal range (10-21 ...", "[BB01.Z] Pulmonary hypertension, unspecified\n --PARENT--> [BB01] Pulmonary hypertension\n Def: Pulmonary hypertension (PH) is a haemodynamic and pathophysiological condition defined as an increase in mean pulmonary arterial pressure (PAP) 25 mmHg at rest as assessed by right heart catheterizati...\n --CHILD--> [BB01.1] Pulmonary hypertension due to left heart disease", "[BB01.Z] Pulmonary hypertension, unspecified\n --PARENT--> [BB01] Pulmonary hypertension\n Def: Pulmonary hypertension (PH) is a haemodynamic and pathophysiological condition defined as an increase in mean pulmonary arterial pressure (PAP) 25 mmHg at rest as assessed by right heart catheterizati...\n --CHILD--> [BB01.1] Pulmonary hypertension due to left heart disease" ]
BA00.Z
Essential hypertension, unspecified
[ { "from_icd11": "BA00.Z", "icd10_code": "I10", "icd10_title": "Essential (primary) hypertension" }, { "from_icd11": "9C61.01", "icd10_code": "H40053", "icd10_title": "Ocular hypertension, bilateral" }, { "from_icd11": "BB01.Z", "icd10_code": "I270", "icd10_title": "Primary pulmonary hypertension" }, { "from_icd11": "BB01.Z", "icd10_code": "I27", "icd10_title": "Other pulmonary heart diseases" }, { "from_icd11": "JA23", "icd10_code": "O133", "icd10_title": "Gestational [pregnancy-induced] hypertension without significant proteinuria, third trimester" }, { "from_icd11": "JA23", "icd10_code": "O135", "icd10_title": "Gestational [pregnancy-induced] hypertension without significant proteinuria, complicating the puerperium" }, { "from_icd11": "JA23", "icd10_code": "O134", "icd10_title": "Gestational [pregnancy-induced] hypertension without significant proteinuria, complicating childbirth" }, { "from_icd11": "JA23", "icd10_code": "O131", "icd10_title": "Gestational [pregnancy-induced] hypertension without significant proteinuria, first trimester" }, { "from_icd11": "JA23", "icd10_code": "O139", "icd10_title": "Gestational [pregnancy-induced] hypertension without significant proteinuria, unspecified trimester" }, { "from_icd11": "JA23", "icd10_code": "O132", "icd10_title": "Gestational [pregnancy-induced] hypertension without significant proteinuria, second trimester" }, { "from_icd11": "JA23", "icd10_code": "O13", "icd10_title": "Gestational [pregnancy-induced] hypertension without significant proteinuria" }, { "from_icd11": "JA23", "icd10_code": "O133 ", "icd10_title": "" }, { "from_icd11": "JA23", "icd10_code": "O163 ", "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" } ]
I10
Essential (primary) hypertension
Complications were observed in 9 (13.2%) hips, with revision surgery performed in 8 (11.7%) of these cases. Posterior hip dislocation was encountered in 1 patient, requiring open reduction and replacement of the femoral stem to adjust the anteversion angle. Femoral revision, using a larger femoral stem, was performed in 2 hips in the early postoperative period due to non-union and rotational instability at the osteotomy site. A two-stage revision was performed in 2 hips due to septic loosening. A revision was performed in 1 patient in the 3 rd postoperative year due to aseptic loosening of the femoral stem and in the 5 th postoperative year due to acetabular loosening. One case of sciatic nerve dysfunction was observed, although partial recovery was achieved. Fracture of the greater trochanter occurred in 1 hip, which was treated with a trochanteric plate and cable grip at the early postoperative period, with bony union achieved at the 8 th postoperative week . Fig. 4 Radiographs of a 53 years old female with high hip dislocation. a Preoperative anteroposterior view. b Early postoperative radiographic image. Hip was reconstructed at the level of the anatomic hip center by cementless modular total hip arthroplasty combined with transverse osteotomy. Trochanter major fracture was observed and treated with trochanteric plate and cable grip, with bony union achieved at the 8th postoperative week ( c )
3.880859
0.494141
sec[2]/p[2]
en
0.999995
35246184
https://doi.org/10.1186/s13018-022-03025-4
[ "postoperative", "revision", "femoral", "hips", "stem", "union", "loosening", "dislocation", "period", "osteotomy" ]
[ { "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" }, { "code": "BC01/BB9Z", "title": "Pulmonary prosthetic valve failure requiring revision" }, { "code": "BC01/BB6Z", "title": "Mitral prosthetic valve failure requiring revision" }, { "code": "BC01/BB8Z", "title": "Tricuspid prosthetic valve failure requiring revision" }, { "code": "BC01/BB7Z", "title": "Aortic prosthetic valve failure requiring revision" }, { "code": "LB9A.8", "title": "Femoral agenesis or hypoplasia" } ]
=== ICD-11 CODES FOUND === [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 [LB9A.8] Femoral agenesis or hypoplasia Definition: Femoral agenesis/hypoplasia is a rare malformation of variable severity ranging from mild hypoplasia to complete absence of the femur. Also known as: Femoral agenesis or hypoplasia | absence of femur | absent femur | agenesis of femur | congenital absence of femur === GRAPH WALKS === --- Walk 1 --- [NE81.0Z] Haemorrhage or haematoma of other or unspecified site complicating a procedure, not elsewhere classified --PARENT--> [NE81.0] Haemorrhage or haematoma complicating a procedure, not elsewhere classified --RELATED_TO--> [?] Haematoma of obstetric wound --- Walk 2 --- [NE81.0Z] Haemorrhage or haematoma of other or unspecified site complicating a procedure, not elsewhere classified --PARENT--> [NE81.0] Haemorrhage or haematoma complicating a procedure, not elsewhere classified --CHILD--> [NE81.00] 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... --- Walk 3 --- [NE81.3] Postsurgical leak --EXCLUDES--> [?] Tracheostomy malfunction --CHILD--> [?] Infection of tracheostomy stoma --- Walk 4 --- [NE81.3] Postsurgical leak --EXCLUDES--> [?] Malfunction or complication of external stoma of digestive organs --CHILD--> [?] Gastrostomy malfunction --- Walk 5 --- [QF00] Acquired absence of limb --EXCLUDES--> [?] Other acquired deformities of limbs --CHILD--> [?] Flexion deformity --- Walk 6 --- [QF00] Acquired absence of limb --EXCLUDES--> [?] Congenital absence of thigh or lower leg with foot present Def: Any condition caused by the failure of the thigh and lower leg to develop during the antenatal period. These conditions are characterised by direct connection of the foot to the hip.... --CHILD--> [?] Congenital absence of thigh or lower leg with foot present, unilateral
[ "[NE81.0Z] Haemorrhage or haematoma of other or unspecified site complicating a procedure, not elsewhere classified\n --PARENT--> [NE81.0] Haemorrhage or haematoma complicating a procedure, not elsewhere classified\n --RELATED_TO--> [?] Haematoma of obstetric wound", "[NE81.0Z] Haemorrhage or haematoma of other or unspecified site complicating a procedure, not elsewhere classified\n --PARENT--> [NE81.0] Haemorrhage or haematoma complicating a procedure, not elsewhere classified\n --CHILD--> [NE81.00] 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...", "[NE81.3] Postsurgical leak\n --EXCLUDES--> [?] Tracheostomy malfunction\n --CHILD--> [?] Infection of tracheostomy stoma", "[NE81.3] Postsurgical leak\n --EXCLUDES--> [?] Malfunction or complication of external stoma of digestive organs\n --CHILD--> [?] Gastrostomy malfunction", "[QF00] Acquired absence of limb\n --EXCLUDES--> [?] Other acquired deformities of limbs\n --CHILD--> [?] Flexion deformity", "[QF00] Acquired absence of limb\n --EXCLUDES--> [?] Congenital absence of thigh or lower leg with foot present\n Def: Any condition caused by the failure of the thigh and lower leg to develop during the antenatal period. These conditions are characterised by direct connection of the foot to the hip....\n --CHILD--> [?] Congenital absence of thigh or lower leg with foot present, unilateral" ]
NE81.0Z
Haemorrhage or haematoma of other or unspecified site complicating a procedure, not elsewhere classified
[ { "from_icd11": "NE81.0Z", "icd10_code": "T8383XA", "icd10_title": "Hemorrhage due to genitourinary prosthetic devices, implants and grafts, initial encounter" }, { "from_icd11": "NE81.0Z", "icd10_code": "T82838A", "icd10_title": "Hemorrhage due to vascular prosthetic devices, implants and grafts, initial encounter" }, { "from_icd11": "NE81.0Z", "icd10_code": "T810", "icd10_title": "" }, { "from_icd11": "QF00", "icd10_code": "Z89412", "icd10_title": "Acquired absence of left great toe" }, { "from_icd11": "QF00", "icd10_code": "Z89611", "icd10_title": "Acquired absence of right leg above knee" }, { "from_icd11": "QF00", "icd10_code": "Z89421", "icd10_title": "Acquired absence of other right toe(s)" }, { "from_icd11": "QF00", "icd10_code": "Z89431", "icd10_title": "Acquired absence of right foot" }, { "from_icd11": "QF00", "icd10_code": "Z89522", "icd10_title": "Acquired absence of left knee" }, { "from_icd11": "QF00", "icd10_code": "Z89411", "icd10_title": "Acquired absence of right great toe" }, { "from_icd11": "QF00", "icd10_code": "Z89511", "icd10_title": "Acquired absence of right leg below knee" }, { "from_icd11": "QF00", "icd10_code": "Z89429", "icd10_title": "Acquired absence of other toe(s), unspecified side" }, { "from_icd11": "QF00", "icd10_code": "Z89422", "icd10_title": "Acquired absence of other left toe(s)" }, { "from_icd11": "QF00", "icd10_code": "Z89211", "icd10_title": "Acquired absence of right upper limb below elbow" }, { "from_icd11": "QF00", "icd10_code": "Z89612", "icd10_title": "Acquired absence of left leg above knee" }, { "from_icd11": "QF00", "icd10_code": "Z89512", "icd10_title": "Acquired absence of left leg below knee" } ]
T8383XA
Hemorrhage due to genitourinary prosthetic devices, implants and grafts, initial encounter
A 12-month-old girl was referred to the Medical Genetics and Rare Disease Center due to gross motor developmental delay and spasticity. The patient had been born at 38 weeks of gestation without any complications. She was the first child born to non-consanguineous parents. Her birth weight was 2.55 kg, and there were no perinatal problems or specific family history of interest. The patient's growth parameters were height, 70 cm (10th centile); weight, 7.8 kg (3rd centile); and head circumference, 41 cm (below the 1st centile). She had no definite dysmorphic features and could roll over but could not sit alone, even with support. On neurological examination, the deep tendon reflexes of both the knee and ankle were exaggerated. Additionally, primitive reflexes were exaggerated. Spasticity was prominent in both lower limbs and was rated as Modified Ashworth Scale Grade I+. Dyskinetic movement was not definite. On Bayley Scales of Infant and Toddler Development (3rd edition), her development corresponded to an equivalent age of 4 months in cognition, 4 months in receptive language, 9 months in expressive language, 4 months in fine motor skills, and 4 months in gross motor skills. Brain magnetic resonance imaging was normal. Due to the discrepancy of clinical manifestations and radiologic findings, Chromosome analysis, CMA, and NGS tests for hereditary developmental delay were simultaneously performed.
4.050781
0.978027
sec[2]/p[0]
en
0.999997
37416820
https://doi.org/10.3389/fped.2023.1201080
[ "motor", "centile", "gross", "developmental", "delay", "spasticity", "born", "weight", "definite", "reflexes" ]
[ { "code": "MB47.0", "title": "Abnormal reflex" }, { "code": "PA2Z", "title": "Unintentional land transport injury event unknown whether traffic or nontraffic injuring a user of unspecified transport" }, { "code": "DA21.Z", "title": "Motility disorders of oesophagus, unspecified" }, { "code": "PA03", "title": "Unintentional land transport traffic event injuring a motor cyclist" }, { "code": "PA20", "title": "Unintentional land transport event unknown whether traffic or nontraffic injuring a pedestrian" }, { "code": "LB00.0", "title": "Congenital diaphragmatic hernia" }, { "code": "MF50.40", "title": "Macroscopic haematuria" }, { "code": "6A04", "title": "Developmental motor coordination disorder" }, { "code": "LD9Z", "title": "Developmental anomalies, unspecified" }, { "code": "6A00.Z", "title": "Disorders of intellectual development, unspecified" } ]
=== ICD-11 CODES FOUND === [MB47.0] Abnormal reflex Also known as: Abnormal reflex | reflex disorder | reflex disturbance | motor disturbance | motor disorder Excludes: vasovagal reaction or syncope | hyperactive gag reflex | abnormal pupillary reflex [PA2Z] Unintentional land transport injury event unknown whether traffic or nontraffic injuring a user of unspecified transport Also known as: Unintentional land transport injury event unknown whether traffic or nontraffic injuring a user of unspecified transport | unintentional land transport injury event unknown whether on road or off-road | land transport accident NOS | motor vehicle accident NOS | MVA - [motor vehicle accident] NOS [DA21.Z] Motility disorders of oesophagus, unspecified Also known as: Motility disorders of oesophagus, unspecified | Motility disorders of oesophagus | Dyskinesia of oesophagus | oesophageal dysmotility | oesophageal motility disorder [PA03] Unintentional land transport traffic event injuring a motor cyclist Also known as: Unintentional land transport traffic event injuring a motor cyclist | motorcycle rider injured in transport accident | unintentional land transport accident motorbike | motorbike accident | motorbike traffic accident Excludes: Unintentional land transport traffic event injuring an occupant of a low powered passenger vehicle [PA20] Unintentional land transport event unknown whether traffic or nontraffic injuring a pedestrian Also known as: Unintentional land transport event unknown whether traffic or nontraffic injuring a pedestrian | unintentional crash injuring a pedestrian, unknown whether on road | pedestrian accident NOS | pedestrian struck by motor vehicle | pedestrian struck by vehicle [LB00.0] Congenital diaphragmatic hernia Definition: 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 hypertension with high mortality. Also known as: Congenital diaphragmatic hernia | congenital diaphragm hernia | congenital diaphragm defect with hernia | gross congenital diaphragm defect | Bochdalek hernia Excludes: Congenital hiatus hernia [MF50.40] Macroscopic haematuria Also known as: Macroscopic haematuria | Gross haematuria | Macroscopic haematuria of urinary tract origin | Macroscopic haematuria of urinary tract origin, intermittent | Macroscopic haematuria of urinary tract origin, persistent [6A04] Developmental motor coordination disorder Definition: Developmental motor coordination disorder is characterised by a significant delay in the acquisition of gross and fine motor skills and impairment in the execution of coordinated motor skills that manifest in clumsiness, slowness, or inaccuracy of motor performance. Coordinated motor skills are markedly below that expected given the individual's chronological age and level of intellectual functioning. Onset of coordinated motor skills difficulties occurs during the developmental period and is ty Also known as: Developmental motor coordination disorder | Developmental coordination disorder | Specific developmental disorder of motor function | 'clumsy child' syndrome | developmental dyspraxia Includes: Orofacial motor coordination disorder Excludes: Abnormalities of gait or mobility | Diseases of the musculoskeletal system or connective tissue | Diseases of the nervous system [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 [6A00.Z] Disorders of intellectual development, unspecified Also known as: Disorders of intellectual development, unspecified | Disorders of intellectual development | Mental retardation | Intellectual developmental disorder | Intellectual disability === GRAPH WALKS === --- Walk 1 --- [MB47.0] Abnormal reflex --EXCLUDES--> [?] Syncope or collapse Def: Syncope is also called fainting, temporary loss of consciousness. Syncope and collapse is temporary loss of consciousness with a fall down.... --CHILD--> [?] Syncope due to autonomic failure --- Walk 2 --- [MB47.0] Abnormal reflex --EXCLUDES--> [?] Syncope or collapse Def: Syncope is also called fainting, temporary loss of consciousness. Syncope and collapse is temporary loss of consciousness with a fall down.... --EXCLUDES--> [?] Shock during or following labour or delivery Def: A syndrome characterised by systemic cellular hypoxia and organ dysfunction as a result of hypoperfusion following labour and delivery. This syndrome is caused by haemorrhage, vomiting, diarrhoea, ina... --- Walk 3 --- [PA2Z] Unintentional land transport injury event unknown whether traffic or nontraffic injuring a user of unspecified transport --PARENT--> [?] Unintentional land transport injury event unknown whether road traffic or off-road nontraffic --CHILD--> [PA20] Unintentional land transport event unknown whether traffic or nontraffic injuring a pedestrian --- Walk 4 --- [PA2Z] Unintentional land transport injury event unknown whether traffic or nontraffic injuring a user of unspecified transport --PARENT--> [?] Unintentional land transport injury event unknown whether road traffic or off-road nontraffic --PARENT--> [?] Unintentional transport injury event Def: !markdown [Definitions in relation to transport injury events] (https://icdcdn.who.int/icd11referenceguide/en/html/index.html#descriptions-related-to-transport-injury-events)... --- Walk 5 --- [DA21.Z] Motility disorders of oesophagus, unspecified --PARENT--> [DA21] Motility disorders of oesophagus Def: This group incorporates oesophageal disorders due to disturbances of oesophageal motor function.... --CHILD--> [DA21.1] Motility disorder of cervical or upper oesophagus Def: Motility disorder of cervical and upper oesophagus is a condition characterised by choke, swallow air, regurgitate fluid into the nose, or experience discomfort in swallowing food due to incompetence ... --- Walk 6 --- [DA21.Z] Motility disorders of oesophagus, unspecified --PARENT--> [DA21] Motility disorders of oesophagus Def: This group incorporates oesophageal disorders due to disturbances of oesophageal motor function.... --CHILD--> [DA21.1] Motility disorder of cervical or upper oesophagus Def: Motility disorder of cervical and upper oesophagus is a condition characterised by choke, swallow air, regurgitate fluid into the nose, or experience discomfort in swallowing food due to incompetence ...
[ "[MB47.0] Abnormal reflex\n --EXCLUDES--> [?] Syncope or collapse\n Def: Syncope is also called fainting, temporary loss of consciousness. Syncope and collapse is temporary loss of consciousness with a fall down....\n --CHILD--> [?] Syncope due to autonomic failure", "[MB47.0] Abnormal reflex\n --EXCLUDES--> [?] Syncope or collapse\n Def: Syncope is also called fainting, temporary loss of consciousness. Syncope and collapse is temporary loss of consciousness with a fall down....\n --EXCLUDES--> [?] Shock during or following labour or delivery\n Def: A syndrome characterised by systemic cellular hypoxia and organ dysfunction as a result of hypoperfusion following labour and delivery. This syndrome is caused by haemorrhage, vomiting, diarrhoea, ina...", "[PA2Z] Unintentional land transport injury event unknown whether traffic or nontraffic injuring a user of unspecified transport\n --PARENT--> [?] Unintentional land transport injury event unknown whether road traffic or off-road nontraffic\n --CHILD--> [PA20] Unintentional land transport event unknown whether traffic or nontraffic injuring a pedestrian", "[PA2Z] Unintentional land transport injury event unknown whether traffic or nontraffic injuring a user of unspecified transport\n --PARENT--> [?] Unintentional land transport injury event unknown whether road traffic or off-road nontraffic\n --PARENT--> [?] Unintentional transport injury event\n Def: !markdown\n[Definitions in relation to transport injury events]\n(https://icdcdn.who.int/icd11referenceguide/en/html/index.html#descriptions-related-to-transport-injury-events)...", "[DA21.Z] Motility disorders of oesophagus, unspecified\n --PARENT--> [DA21] Motility disorders of oesophagus\n Def: This group incorporates oesophageal disorders due to disturbances of oesophageal motor function....\n --CHILD--> [DA21.1] Motility disorder of cervical or upper oesophagus\n Def: Motility disorder of cervical and upper oesophagus is a condition characterised by choke, swallow air, regurgitate fluid into the nose, or experience discomfort in swallowing food due to incompetence ...", "[DA21.Z] Motility disorders of oesophagus, unspecified\n --PARENT--> [DA21] Motility disorders of oesophagus\n Def: This group incorporates oesophageal disorders due to disturbances of oesophageal motor function....\n --CHILD--> [DA21.1] Motility disorder of cervical or upper oesophagus\n Def: Motility disorder of cervical and upper oesophagus is a condition characterised by choke, swallow air, regurgitate fluid into the nose, or experience discomfort in swallowing food due to incompetence ..." ]
MB47.0
Abnormal reflex
[ { "from_icd11": "MB47.0", "icd10_code": "R292", "icd10_title": "Abnormal reflex" }, { "from_icd11": "PA2Z", "icd10_code": "V988XXS", "icd10_title": "Other specified transport accidents, sequela" }, { "from_icd11": "PA2Z", "icd10_code": "V99XXXD", "icd10_title": "Unspecified transport accident, subsequent encounter" }, { "from_icd11": "PA2Z", "icd10_code": "V988XXA", "icd10_title": "Other specified transport accidents, initial encounter" }, { "from_icd11": "PA2Z", "icd10_code": "V99XXXS", "icd10_title": "Unspecified transport accident, sequela" }, { "from_icd11": "PA2Z", "icd10_code": "V80010A", "icd10_title": "Animal-rider injured by fall from or being thrown from horse in noncollision accident, initial encounter" }, { "from_icd11": "PA2Z", "icd10_code": "V899XXS", "icd10_title": "Person injured in unspecified vehicle accident, sequela" }, { "from_icd11": "PA2Z", "icd10_code": "V80919A", "icd10_title": "Animal-rider injured in unspecified transport accident, initial encounter" }, { "from_icd11": "PA2Z", "icd10_code": "V899XXA", "icd10_title": "Person injured in unspecified vehicle accident, initial encounter" }, { "from_icd11": "PA2Z", "icd10_code": "V8011XA", "icd10_title": "Animal-rider injured in collision with pedestrian or animal, initial encounter" }, { "from_icd11": "PA2Z", "icd10_code": "V8041XA", "icd10_title": "Animal-rider injured in collision with car, pick-up truck, van, heavy transport vehicle or bus, initial encounter" }, { "from_icd11": "PA2Z", "icd10_code": "V8012XA", "icd10_title": "Occupant of animal-drawn vehicle injured in collision with pedestrian or animal, initial encounter" }, { "from_icd11": "PA2Z", "icd10_code": "V8021XA", "icd10_title": "Animal-rider injured in collision with pedal cycle, initial encounter" }, { "from_icd11": "PA2Z", "icd10_code": "V899", "icd10_title": "Person injured in unspecified vehicle accident" }, { "from_icd11": "PA2Z", "icd10_code": "V98-V99", "icd10_title": "" } ]
R292
Abnormal reflex
A 15-year-old, previously healthy boy without a history of smoking or drug abuse, admitted to the hospital with acute epigastric pain without dyspnea or heartburn. On physical examination the boy was pale with tachycardia (110/min), but normal blood pressure (110/70 mmHg) and normal capillary oxygen saturation in room air (SPO2 99%). Tenderness in the upper abdomen was present. Laboratory investigations showed mild iron deficiency anemia (haemoglobin concentration 7.1 mmol/l, mean cellular volume 65 fl, serum iron 4 mmol/l, serum ferritin 3 g/l) with normal infection parameters. X-ray revealed free air under the right diaphragm. Abdominal ultrasound and CT scan were performed in search of underlying abnormalities, but none could be detected. At laparotomy, gastric perforation was found, which was repaired after refreshing the margins and tissue was sent for histopathology. Histopathology of the fragments showed ulceration without demonstrable Helicobacter pylori; recognizable mucosa was lacking. Subsequent gastro-duodenoscopy showed macroscopically a nodular aspect of the corpus with remarkably coarse gastric folds and pseudo-polyps . Histological examination of gastric biopsies showed active chronic inflammation with lympho-plasma-cellular infiltration and a thickened sub-epithelial collagenous band, up to 23 μm, consistent with the diagnosis collagenous gastritis; the duodenal mucosa was normal.
3.998047
0.981445
sec[0]/p[0]
en
0.999998
26816680
N/A
[ "without", "gastric", "iron", "mmol", "cellular", "serum", "histopathology", "mucosa", "collagenous", "previously" ]
[ { "code": "MH12.1", "title": "Death occurring less than 24 hours from onset of symptoms, not otherwise explained" }, { "code": "FA36.Y", "title": "Other specified effusion of joint" }, { "code": "3A51.1", "title": "Sickle cell disease without crisis" }, { "code": "QA50", "title": "Embolisation without injury or harm" }, { "code": "LB12.1Z", "title": "Atresia of oesophagus, unspecified" }, { "code": "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" } ]
=== ICD-11 CODES FOUND === [MH12.1] Death occurring less than 24 hours from onset of symptoms, not otherwise explained Also known as: Death occurring less than 24 hours from onset of symptoms, not otherwise explained | died without sign of disease | Death known not to be violent or instantaneous for which no cause can be discovered | death known not to be violent or instantaneous, cause unknown | Death without sign of disease Includes: Death known not to be violent or instantaneous for which no cause can be discovered | Death without sign of disease [FA36.Y] Other specified effusion of joint Also known as: Other specified effusion of joint | Non aspirated effusion of joint | Effusion of joint without blood | Effusion of joint, multiple sites | Effusion of joint, shoulder region [3A51.1] Sickle cell disease without crisis Definition: A disorder caused by a HbS mutation in the haemoglobin gene. This disorder is characterised by abnormal rigid sickle-shaped red blood cells decreasing its ability to carry oxygen. This disorder may present with fatigue, shortness of breath, dizziness, headaches, pallor of skin or mucous membranes, and jaundice. This disorder is confirmed by identification of HbS mutation by genetic testing. Also known as: Sickle cell disease without crisis | Hb-SS disease without crisis | HbSS without crisis | Sickle-cell anaemia without crisis | SCD - [sickle cell disease] [QA50] Embolisation without injury or harm Definition: An embolisation without documented injury or harm occurs when a solid object within the venous or arterial circulation propagates to a distal location and becomes lodged there. Also known as: Embolisation without injury or harm | Embolic phenomenon without documented injury or harm | Air embolism without documented injury or harm | Injection of air without injury or harm Excludes: Embolisation, as mode of injury or harm [LB12.1Z] Atresia of oesophagus, unspecified Also known as: Atresia of oesophagus, unspecified | Atresia of oesophagus | atresia of esophagus | Atresia of oesophagus without fistula | congenital atresia of oesophagus [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 === GRAPH WALKS === --- Walk 1 --- [MH12.1] Death occurring less than 24 hours from onset of symptoms, not otherwise explained --PARENT--> [MH12] Other sudden death, cause unknown --CHILD--> [MH12.Y] Other specified sudden death, cause unknown --- Walk 2 --- [MH12.1] Death occurring less than 24 hours from onset of symptoms, not otherwise explained --PARENT--> [MH12] Other sudden death, cause unknown --EXCLUDES--> [?] Sudden infant death syndrome Def: Sudden infant death syndrome is the abrupt and unexplained death of an apparently healthy infant under one year of age, remaining unexplained after a thorough case investigation, including performance... --- Walk 3 --- [FA36.Y] Other specified effusion of joint --PARENT--> [FA36] Effusion of joint Def: Increased intra-articular fluid secondary to trauma and/or other acquired conditions not detailed in other codes.... --PARENT--> [?] Certain specified joint disorders or deformities of limbs --- Walk 4 --- [FA36.Y] Other specified effusion of joint --PARENT--> [FA36] Effusion of joint Def: Increased intra-articular fluid secondary to trauma and/or other acquired conditions not detailed in other codes.... --PARENT--> [?] Certain specified joint disorders or deformities of limbs --- Walk 5 --- [3A51.1] Sickle cell disease without crisis Def: A disorder caused by a HbS mutation in the haemoglobin gene. This disorder is characterised by abnormal rigid sickle-shaped red blood cells decreasing its ability to carry oxygen. This disorder may pr... --PARENT--> [3A51] Sickle cell disorders or other haemoglobinopathies Def: Any disorder caused by a HbS mutation in the haemoglobin gene. This disorder is characterised by abnormal rigid sickle-shaped red blood cells decreasing its ability to carry oxygen. This disorder may ... --RELATED_TO--> [?] Other sickle-cell disorders with retinopathy Def: This is an autosomal recessive genetic blood disorder with overdominance, characterised by red blood cells that assume an abnormal, rigid, sickle shape. This diagnosis is due to persistent or acute da... --- Walk 6 --- [3A51.1] Sickle cell disease without crisis Def: A disorder caused by a HbS mutation in the haemoglobin gene. This disorder is characterised by abnormal rigid sickle-shaped red blood cells decreasing its ability to carry oxygen. This disorder may pr... --PARENT--> [3A51] Sickle cell disorders or other haemoglobinopathies Def: Any disorder caused by a HbS mutation in the haemoglobin gene. This disorder is characterised by abnormal rigid sickle-shaped red blood cells decreasing its ability to carry oxygen. This disorder may ... --RELATED_TO--> [?] Osteonecrosis due to haemoglobinopathy
[ "[MH12.1] Death occurring less than 24 hours from onset of symptoms, not otherwise explained\n --PARENT--> [MH12] Other sudden death, cause unknown\n --CHILD--> [MH12.Y] Other specified sudden death, cause unknown", "[MH12.1] Death occurring less than 24 hours from onset of symptoms, not otherwise explained\n --PARENT--> [MH12] Other sudden death, cause unknown\n --EXCLUDES--> [?] Sudden infant death syndrome\n Def: Sudden infant death syndrome is the abrupt and unexplained death of an apparently healthy infant under one year of age, remaining unexplained after a thorough case investigation, including performance...", "[FA36.Y] Other specified effusion of joint\n --PARENT--> [FA36] Effusion of joint\n Def: Increased intra-articular fluid secondary to trauma and/or other acquired conditions not detailed in other codes....\n --PARENT--> [?] Certain specified joint disorders or deformities of limbs", "[FA36.Y] Other specified effusion of joint\n --PARENT--> [FA36] Effusion of joint\n Def: Increased intra-articular fluid secondary to trauma and/or other acquired conditions not detailed in other codes....\n --PARENT--> [?] Certain specified joint disorders or deformities of limbs", "[3A51.1] Sickle cell disease without crisis\n Def: A disorder caused by a HbS mutation in the haemoglobin gene. This disorder is characterised by abnormal rigid sickle-shaped red blood cells decreasing its ability to carry oxygen. This disorder may pr...\n --PARENT--> [3A51] Sickle cell disorders or other haemoglobinopathies\n Def: Any disorder caused by a HbS mutation in the haemoglobin gene. This disorder is characterised by abnormal rigid sickle-shaped red blood cells decreasing its ability to carry oxygen. This disorder may ...\n --RELATED_TO--> [?] Other sickle-cell disorders with retinopathy\n Def: This is an autosomal recessive genetic blood disorder with overdominance, characterised by red blood cells that assume an abnormal, rigid, sickle shape. This diagnosis is due to persistent or acute da...", "[3A51.1] Sickle cell disease without crisis\n Def: A disorder caused by a HbS mutation in the haemoglobin gene. This disorder is characterised by abnormal rigid sickle-shaped red blood cells decreasing its ability to carry oxygen. This disorder may pr...\n --PARENT--> [3A51] Sickle cell disorders or other haemoglobinopathies\n Def: Any disorder caused by a HbS mutation in the haemoglobin gene. This disorder is characterised by abnormal rigid sickle-shaped red blood cells decreasing its ability to carry oxygen. This disorder may ...\n --RELATED_TO--> [?] Osteonecrosis due to haemoglobinopathy" ]
MH12.1
Death occurring less than 24 hours from onset of symptoms, not otherwise explained
[ { "from_icd11": "MH12.1", "icd10_code": "R961", "icd10_title": "" }, { "from_icd11": "3A51.1", "icd10_code": "D571", "icd10_title": "Sickle-cell disease without crisis" }, { "from_icd11": "QA50", "icd10_code": "XXI", "icd10_title": "" }, { "from_icd11": "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" } ]
R961
An aberrant right subclavian artery (ARSA) is a rare congenital malformation, wherein the aorta gives rise to the right subclavian artery as a branch off the aortic arch distal to the takeoff of the left subclavian artery. Although rare, an ARSA is the most common congenital anomaly of the great vessels, with a reported incidence between 0.5 and 1.8% . In the majority of cases, the ARSA courses posterior to the esophagus en route to the right side of the body . Nearly 60% of the time, a concurrent Kommerell’s diverticulum (KD), or an aneurysm-like dilation of the proximal opening of the ARSA, is present . This diverticulum often compresses nearby structures, resulting in symptomatic dysphagia, known as ‘dysphagia lusoria’. Although dysphagia lusoria is well documented in the literature, we present a rare case of a patient with an ARSA that manifested vertebrobasilar symptoms. We also conducted a review of pertinent literature. As opposed to a KD, which is a dilation of the ARSA, our patient had severe stenosis of the ARSA at the origin, which led to retrograde blood flow through the right vertebral artery and decreased flow to the hand. The reversal of blood flow in the vertebral artery resulted in hypoperfusion to the posterior brain, which caused vertebrobasilar symptoms and claudication of the right hand and arm. Patient agreed to proceed with posting the details and images in this case report.
4.191406
0.928711
sec[0]/p[0]
en
0.999996
PMC10125837
https://doi.org/10.1093/jscr/rjad199
[ "arsa", "artery", "subclavian", "rare", "dysphagia", "which", "flow", "congenital", "although", "diverticulum" ]
[ { "code": "LA8B.24", "title": "Congenital anomaly of aortic arch branch" }, { "code": "BD5Z", "title": "Diseases of arteries or arterioles, unspecified" }, { "code": "BD52", "title": "Certain specified disorders of arteries or arterioles" }, { "code": "BD52.3", "title": "Rupture of artery" }, { "code": "BD52.2", "title": "Stricture of artery" }, { "code": "BD40.Z", "title": "Atherosclerotic chronic arterial occlusive disease, unspecified" }, { "code": "8B22.A", "title": "Subclavian steal syndrome" }, { "code": "BD30.00&XA5D68", "title": "Acute thromboembolic subclavian artery occlusion" }, { "code": "BD30.01&XA5D68", "title": "Acute thrombotic subclavian artery occlusion" }, { "code": "NB30.1Y", "title": "Other specified injury of innominate or subclavian artery" } ]
=== ICD-11 CODES FOUND === [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] [BD5Z] Diseases of arteries or arterioles, unspecified Also known as: Diseases of arteries or arterioles, unspecified | artery disease NOS | arterial disease NOS | arteriolar disease NOS | disorder of artery NOS [BD52] Certain specified disorders of arteries or arterioles Also known as: Certain specified disorders of arteries or arterioles | Aortic dilatation - joint hypermobility - arterial tortuosity | Generalised arterial calcification of infancy | Median arcuate ligament syndrome | Aortic root abscess Excludes: collagen (vascular) diseases | Hypersensitivity angiitis | Acute arterial occlusion [BD52.3] Rupture of artery Also known as: Rupture of artery | ruptured artery | artery fistula | Aortic duodenal fistula | Aortic colon fistula Excludes: traumatic rupture of artery - see injury of blood vessel by body region [BD52.2] Stricture of artery Also known as: Stricture of artery | arterial stenosis | arterial stricture | artery stricture | stenosis of artery [BD40.Z] Atherosclerotic chronic arterial occlusive disease, unspecified Also known as: Atherosclerotic chronic arterial occlusive disease, unspecified | Atherosclerotic chronic arterial occlusive disease | arteriosclerosis, NOS | generalised atherosclerosis | atherosclerosis NOS [8B22.A] Subclavian steal syndrome Definition: Retrograde blood flow in the vertebral artery in the setting of ipsilateral proximal subclavian artery stenosis or occlusion leading to symptoms of basilar insufficiency. Also known as: Subclavian steal syndrome | subclavian artery stenosis [NB30.1Y] Other specified injury of innominate or subclavian artery Also known as: Other specified injury of innominate or subclavian artery | Haematoma of subclavian artery === GRAPH WALKS === --- Walk 1 --- [LA8B.24] Congenital anomaly of aortic arch branch Def: A congenital cardiovascular malformation of one or more branches of the aortic arch (innominate, carotid, or subclavian arteries).... --PARENT--> [LA8B.2] Congenital anomaly of aorta or its branches Def: A congenital cardiovascular malformation of the aorta and/or its branches.... --CHILD--> [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... --- Walk 2 --- [LA8B.24] Congenital anomaly of aortic arch branch Def: A congenital cardiovascular malformation of one or more branches of the aortic arch (innominate, carotid, or subclavian arteries).... --PARENT--> [LA8B.2] Congenital anomaly of aorta or its branches Def: A congenital cardiovascular malformation of the aorta and/or its branches.... --CHILD--> [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... --- Walk 3 --- [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 4 --- [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 5 --- [BD52] Certain specified disorders of arteries or arterioles --EXCLUDES--> [?] Leukocytoclastic vasculitis Def: Leukocytoclastic vasculitis (hypersensitivity vasculitis; hypersensitivity angiitis) is a histopathological term commonly used to denote a small-vessel vasculitis. It may be localised to the skin or m... --CHILD--> [?] Cutaneous leukocytoclastic vasculitis Def: Skin-limited small vessel leucocytoclastic vasculitis of unspecified or unknown aetiology... --- Walk 6 --- [BD52] Certain specified disorders of arteries or arterioles --CHILD--> [BD52.1] Arteriovenous fistula, acquired --EXCLUDES--> [?] Cerebral aneurysm, nonruptured
[ "[LA8B.24] Congenital anomaly of aortic arch branch\n Def: A congenital cardiovascular malformation of one or more branches of the aortic arch (innominate, carotid, or subclavian arteries)....\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.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...", "[LA8B.24] Congenital anomaly of aortic arch branch\n Def: A congenital cardiovascular malformation of one or more branches of the aortic arch (innominate, carotid, or subclavian arteries)....\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.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...", "[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....", "[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. ...", "[BD52] Certain specified disorders of arteries or arterioles\n --EXCLUDES--> [?] Leukocytoclastic vasculitis\n Def: Leukocytoclastic vasculitis (hypersensitivity vasculitis; hypersensitivity angiitis) is a histopathological term commonly used to denote a small-vessel vasculitis. It may be localised to the skin or m...\n --CHILD--> [?] Cutaneous leukocytoclastic vasculitis\n Def: Skin-limited small vessel leucocytoclastic vasculitis of unspecified or unknown aetiology...", "[BD52] Certain specified disorders of arteries or arterioles\n --CHILD--> [BD52.1] Arteriovenous fistula, acquired\n --EXCLUDES--> [?] Cerebral aneurysm, nonruptured" ]
LA8B.24
Congenital anomaly of aortic arch branch
[ { "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
Patient 2 was admitted to a local hospital due to generalized seizures at the age of 10 weeks. Hypoglycaemia (2.4 mmol/L) was verified, but no further investigations were done at the time. This male infant was the first child of non-consanguineous parents, born at term, with a birth weight of 3050 g, a birth length of 49 cm, and an Apgar score 9 at one minute. At the age of six months, seizures reoccurred with hypoglycaemia (1.4 mmol/L), and the patient was referred to our Institute. On admission, the infant had normal physical findings with a weight of 8200 g (62nd centile) and length of 68 cm (50th centile). During the first day of hospitalization, the lowest value of glycaemia was 2.8 mmol/L with a concomitant insulinemia of 19.82 μmol/L and HA of 159.2 μmol/L. EEG pattern was described as normal. Treatment was started with diazoxide (5 mg/kg/day) and hydrochlorothiazide (2 mg/kg/day) with advice for avoiding protein-rich meals. Since the patient missed regular check-ups, the next examination was performed at 20 months of age and speech delay with mild hyperactivity was noted. The parents acknowledged several hypoglycaemic crises (non-seizure) early after treatment introduction. At the age of 3.5 years, physical status was normal while neuropsychological assessment confirmed borderline mental delay (DQ 90 at Brunet-Lézine scale) associated with signs of attention-deficit/hyperactivity disorder.
3.916016
0.98291
sec[1]/p[2]
en
0.999997
26759084
https://doi.org/10.4274/jcrpe.2436
[ "mmol", "seizures", "hypoglycaemia", "parents", "birth", "weight", "length", "physical", "centile", "delay" ]
[ { "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": "8A68.Z", "title": "Type of seizure, unspecified" }, { "code": "8A6Z", "title": "Epilepsy or seizures, unspecified" }, { "code": "8A63.Y", "title": "Seizure due to other acute cause" }, { "code": "8A67", "title": "Acute repetitive seizures" }, { "code": "8A68.Y", "title": "Other specified type of seizure" }, { "code": "5A41", "title": "Hypoglycaemia without associated diabetes" }, { "code": "5A4Z", "title": "Disorders of glucose regulation or pancreatic internal secretion, 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 [8A68.Z] Type of seizure, unspecified Also known as: Type of seizure, unspecified | Types of seizures | uncontrolled seizures | Seizure NOS | fits NOS [8A6Z] Epilepsy or seizures, unspecified Also known as: Epilepsy or seizures, unspecified | Cerebral seizures | Seizure disorder | seizure disorder, so described | epilepsy NOS [8A63.Y] Seizure due to other acute cause Also known as: Seizure due to other acute cause | Seizures due to immune disorders | Seizures due to medications | Toxic syndrome with generalised seizures, drug related | Acute seizures due to central nervous system infections or infestations [8A67] Acute repetitive seizures Definition: Acute repetitive seizures are multiple seizures, with a distinct time of onset, with recovery between each seizure, occurring within 24 hours in adults, or 12 hours in children. Also known as: Acute repetitive seizures | complex partial status epilepticus | Cluster seizures | Serial seizures | Recurrent seizures [8A68.Y] Other specified type of seizure Also known as: Other specified type of seizure | Absence episode | Absence seizure episode | Pseudotetanus | Clonic seizure disorder [5A41] Hypoglycaemia without associated diabetes Also known as: Hypoglycaemia without associated diabetes | low blood sugar | hypoglycaemia NOS | spontaneous hypoglycaemia | nondiabetic hypoglycaemia Excludes: Hypoglycaemia in the context of diabetes mellitus [5A4Z] Disorders of glucose regulation or pancreatic internal secretion, unspecified Also known as: Disorders of glucose regulation or pancreatic internal secretion, unspecified === 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--> [?] Gestational proteinuria without hypertension --- 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--> [?] 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 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... --EXCLUDES--> [?] Gestational proteinuria without hypertension --- 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... --PARENT--> [?] Glomerular diseases Def: Any disease characterised by pathological changes to the glomerulus.... --- Walk 5 --- [MA18.0Y] Other specified elevated blood glucose level --PARENT--> [MA18.0] Elevated blood glucose level --EXCLUDES--> [?] Postprocedural hypoinsulinaemia Def: This is a low level of insulin that can result after medical procedures, including radiation, and it carries a risk of developing diabetes mellitus.... --- Walk 6 --- [MA18.0Y] Other specified elevated blood glucose level --PARENT--> [MA18.0] Elevated blood glucose level --EXCLUDES--> [?] Diabetes mellitus in pregnancy Def: A condition caused by dysfunctional maternal insulin receptors. This condition is characterised by glucose intolerance with onset or first recognition during pregnancy, with at least one of the follow...
[ "[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--> [?] Gestational proteinuria without hypertension", "[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....", "[GB42.0] 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 --EXCLUDES--> [?] Gestational proteinuria without hypertension", "[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 --PARENT--> [?] Glomerular diseases\n Def: Any disease characterised by pathological changes to the glomerulus....", "[MA18.0Y] Other specified elevated blood glucose level\n --PARENT--> [MA18.0] Elevated blood glucose level\n --EXCLUDES--> [?] Postprocedural hypoinsulinaemia\n Def: This is a low level of insulin that can result after medical procedures, including radiation, and it carries a risk of developing diabetes mellitus....", "[MA18.0Y] Other specified elevated blood glucose level\n --PARENT--> [MA18.0] Elevated blood glucose level\n --EXCLUDES--> [?] Diabetes mellitus in pregnancy\n Def: A condition caused by dysfunctional maternal insulin receptors. This condition is characterised by glucose intolerance with onset or first recognition during pregnancy, with at least one of the follow..." ]
GB42.1
Albuminuria, Grade A3
[ { "from_icd11": "8A68.Z", "icd10_code": "R561", "icd10_title": "Post traumatic seizures" }, { "from_icd11": "8A68.Z", "icd10_code": "R569", "icd10_title": "Unspecified convulsions" }, { "from_icd11": "8A68.Z", "icd10_code": "R56", "icd10_title": "Convulsions, not elsewhere classified" }, { "from_icd11": "8A68.Z", "icd10_code": "R568", "icd10_title": "" }, { "from_icd11": "8A6Z", "icd10_code": "G40A09", "icd10_title": "Absence epileptic syndrome, not intractable, without status epilepticus" }, { "from_icd11": "8A6Z", "icd10_code": "G40B09", "icd10_title": "Juvenile myoclonic epilepsy, not intractable, without status epilepticus" }, { "from_icd11": "8A6Z", "icd10_code": "G40B19", "icd10_title": "Juvenile myoclonic epilepsy, intractable, without status epilepticus" }, { "from_icd11": "8A6Z", "icd10_code": "G40A19", "icd10_title": "Absence epileptic syndrome, intractable, without status epilepticus" }, { "from_icd11": "8A6Z", "icd10_code": "G40A11", "icd10_title": "Absence epileptic syndrome, intractable, with status epilepticus" }, { "from_icd11": "8A6Z", "icd10_code": "G40A01", "icd10_title": "Absence epileptic syndrome, not intractable, with status epilepticus" }, { "from_icd11": "8A6Z", "icd10_code": "G40409", "icd10_title": "Other generalized epilepsy and epileptic syndromes, not intractable, without status epilepticus" }, { "from_icd11": "8A6Z", "icd10_code": "G40802", "icd10_title": "Other epilepsy, not intractable, without status epilepticus" }, { "from_icd11": "8A6Z", "icd10_code": "G40801", "icd10_title": "Other epilepsy, not intractable, with status epilepticus" }, { "from_icd11": "8A6Z", "icd10_code": "G40901", "icd10_title": "Epilepsy, unspecified, not intractable, with status epilepticus" }, { "from_icd11": "8A6Z", "icd10_code": "G4089", "icd10_title": "Other seizures" } ]
R561
Post traumatic seizures
The children of the index case (patients 2.1–2.3) were screened from birth and diagnosed with glucocorticoid deficiency between the ages of 0.1 and 6.9 years. Patient 2.5 presented at 0.1 year with cardiac failure secondary to congenital truncus arteriosus and a ventricular septal defect. During his admission he was diagnosed with isolated glucocorticoid deficiency. He is the only affected member of the kindred known to have comorbidity. Echocardiograms and electrocardiograms were normal in all individuals homozygous for the mutation except patient 1.2, who has trivial tricuspid and mitral valve regurgitation. All clinically affected individuals demonstrated a poor cortisol response to ACTH stimulation [125 μg tetracosactide (Synacthen) im] requiring standard glucocorticoid replacement therapy. All have normal mineralocorticoid production. Patient 2.4, homozygous for the TXNRD2 mutation, is currently clinically well aged 7.4 years with normal biochemistry and is under close clinical surveillance. Interestingly, she has had raised ACTH levels in early infancy (9:00 am ACTH of 124 ng/L at 0.02 y of age; corresponding cortisol of 305 nmol/L), which subsequently normalized. Her older sister, individual 2.2, similarly had raised ACTH levels in infancy (9:00 am ACTH 171 ng/L at 0.98 y of age; corresponding cortisol of 448 nmol/L), which normalized, although she was later diagnosed with FGD at 6.9 years.
4.191406
0.581055
sec[2]/p[1]
en
0.999998
24601690
https://doi.org/10.1210/jc.2013-3844
[ "acth", "diagnosed", "glucocorticoid", "cortisol", "deficiency", "affected", "individuals", "homozygous", "mutation", "clinically" ]
[ { "code": "5A74.Y", "title": "Other specified adrenocortical insufficiency" }, { "code": "5A70.1", "title": "Ectopic ACTH syndrome" }, { "code": "5A70.Z", "title": "Cushing syndrome, unspecified" }, { "code": "5A70.Y", "title": "Other specified Cushing syndrome" }, { "code": "5A70.0", "title": "Pituitary-dependent Cushing disease" }, { "code": "1F45", "title": "Malaria without parasitological confirmation" }, { "code": "RA01.1", "title": "COVID-19, virus not identified" }, { "code": "5A71.00", "title": "Glucocorticoid resistance" }, { "code": "NE60", "title": "Harmful effects of drugs, medicaments or biological substances, not elsewhere classified" }, { "code": "5A72.0", "title": "Primary hyperaldosteronism" } ]
=== ICD-11 CODES FOUND === [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 [5A70.1] Ectopic ACTH syndrome Also known as: Ectopic ACTH syndrome | Cushing syndrome secondary to ectopic ACTH-secretion | Ectopic Cushing syndrome | hypercortisolism due to nonpituitary tumour | ectopic ACTH - [adrenocorticotropic hormone] secretion [5A70.Z] Cushing syndrome, unspecified Also known as: Cushing syndrome, unspecified | Cushing syndrome | Hyperadrenocorticism | Hypercortisolism | Cushing syndrome NOS [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 [5A70.0] Pituitary-dependent Cushing disease Definition: Pituitary-dependent Cushing disease is caused by a pituitary tumour, generally benign (adenoma) but rarely malignant (carcinoma), which secretes adrenocorticotropin (ACTH) autonomously, leading to hypercortisolism. The condition is associated with increased morbidity and mortality that can be mitigated by treatments that result in sustained endocrine remission. Transsphenoidal pituitary surgery (TSS) remains the mainstay of treatment for this disease but requires considerable neurosurgical exper Also known as: Pituitary-dependent Cushing disease | Overproduction of pituitary ACTH | Pituitary-dependent hyperadrenocorticism | Corticotroph pituitary adenoma | ACTH- [adrenocorticotropic hormone] secreting pituitary adenoma [1F45] Malaria without parasitological confirmation Definition: Clinically diagnosed malaria without parasitological confirmation Also known as: Malaria without parasitological confirmation | marsh fever | remittent congestive fever | coastal fever | remittent gastric fever Includes: clinically diagnosed malaria without parasitological confirmation [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 [5A71.00] Glucocorticoid resistance Definition: Glucocorticoid resistance is a rare genetic endocrine condition characterised by generalised, partial, target tissue resistance to glucocorticoids. The clinical spectrum of the condition is broad, ranging from asymptomatic to severe cases of hyperandrogenism, fatigue and/or mineralocorticoid excess. Also known as: Glucocorticoid 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 [5A72.0] Primary hyperaldosteronism Also known as: Primary hyperaldosteronism | idiopathic aldosteronism | primary aldosteronism | Conn syndrome | Aldosteronism === GRAPH WALKS === --- Walk 1 --- [5A74.Y] Other specified adrenocortical insufficiency --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 2 --- [5A74.Y] Other specified adrenocortical insufficiency --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 3 --- [5A70.1] Ectopic ACTH 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--> [5A70.1] Ectopic ACTH syndrome --- Walk 4 --- [5A70.1] Ectopic ACTH 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--> [5A70.1] Ectopic ACTH syndrome --- Walk 5 --- [5A70.Z] Cushing syndrome, unspecified --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--> [5A70.2] Pseudo-Cushing syndrome Def: This is a condition in which patients display the signs, symptoms, and abnormal hormone levels seen in Cushing's syndrome. However, pseudo-Cushing's syndrome is not caused by a problem with the hypoth... --- Walk 6 --- [5A70.Z] Cushing syndrome, unspecified --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--> [5A70.1] Ectopic ACTH syndrome
[ "[5A74.Y] Other specified adrenocortical insufficiency\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.Y] Other specified adrenocortical insufficiency\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....", "[5A70.1] Ectopic ACTH 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--> [5A70.1] Ectopic ACTH syndrome", "[5A70.1] Ectopic ACTH 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--> [5A70.1] Ectopic ACTH syndrome", "[5A70.Z] Cushing syndrome, unspecified\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--> [5A70.2] Pseudo-Cushing syndrome\n Def: This is a condition in which patients display the signs, symptoms, and abnormal hormone levels seen in Cushing's syndrome. However, pseudo-Cushing's syndrome is not caused by a problem with the hypoth...", "[5A70.Z] Cushing syndrome, unspecified\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--> [5A70.1] Ectopic ACTH syndrome" ]
5A74.Y
Other specified adrenocortical insufficiency
[ { "from_icd11": "5A70.1", "icd10_code": "E243", "icd10_title": "Ectopic ACTH syndrome" }, { "from_icd11": "5A70.Z", "icd10_code": "E242", "icd10_title": "Drug-induced Cushing's syndrome" }, { "from_icd11": "5A70.Z", "icd10_code": "E249", "icd10_title": "Cushing's syndrome, unspecified" }, { "from_icd11": "5A70.Z", "icd10_code": "E248", "icd10_title": "Other Cushing's syndrome" }, { "from_icd11": "5A70.Z", "icd10_code": "E24", "icd10_title": "Cushing's syndrome" }, { "from_icd11": "5A70.0", "icd10_code": "E240", "icd10_title": "Pituitary-dependent Cushing's disease" }, { "from_icd11": "1F45", "icd10_code": "B54", "icd10_title": "Unspecified malaria" }, { "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" } ]
E243
Ectopic ACTH syndrome
Diagnosis of ischemic/low-flow priapism was integrated. Physicians proceeded to perform lavage and aspiration of the corpora cavernosa with phenylephrine every three to five minutes for a period of one hour, with a partial decrease in tumescence for approximately two hours. The patient subsequently presented a recurrence of tumescence and pain, for which he was admitted to the operating room. A Winter-type distal cavernotomy was carried out, but no remission or decrease in tumescence was achieved. Then an Al Ghorab-type open distal bypass was performed and a decrease in tumescence of approximately 40% was obtained for a period of 48 hours, after which tumescence and pain increased. The patient was once again rushed to the operating room and underwent a spongiosum-cavernous fistula (Quackels technique). Since a decrease in tumescence was not achieved and due to persistent pain, the patient was referred to our third-level care center to continue his management. Upon admission, the patient was found with a painful erection on palpation, with total tumescence and rigidity of both corpora cavernosa, with injuries to the glans and base of the penis corresponding to the procedures performed in the referral medical unit. A penile Doppler ultrasound was carried out to find decreased cavernous arterial flow compatible with persistent ischemic priapism. The toxicological and hematological panel was negative.
3.751953
0.98291
sec[1]/p[1]
en
0.999996
PMC10315176
https://doi.org/10.7759/cureus.39882
[ "tumescence", "decrease", "pain", "ischemic", "flow", "priapism", "corpora", "cavernosa", "period", "approximately" ]
[ { "code": "4B4Z", "title": "Diseases of the immune system, unspecified" }, { "code": "MC1Y", "title": "Other specified symptoms or signs involving the visual system" }, { "code": "AB52", "title": "Deafness not otherwise specified" }, { "code": "MG22", "title": "Fatigue" }, { "code": "MG43.8", "title": "Decreased appetite" }, { "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 === [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 [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 [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 [MG43.8] Decreased appetite Definition: Intermittent or persistent decreased motivation or desire to eat food as compared to what is typical for the individual. Also known as: Decreased appetite [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 --- [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 2 --- [4B4Z] Diseases of the immune system, unspecified --PARENT--> [04] Diseases of the immune system --CHILD--> [4A20] Acquired immunodeficiencies --- Walk 3 --- [MC1Y] Other specified symptoms or signs involving the visual system --PARENT--> [?] Symptoms or signs involving the visual system --CHILD--> [MC12] Chronic enlargement of lacrimal gland --- Walk 4 --- [MC1Y] Other specified symptoms or signs involving the visual system --PARENT--> [?] Symptoms or signs involving the visual system --CHILD--> [MC10] Eye appearance abnormal --- Walk 5 --- [AB52] Deafness not otherwise specified --PARENT--> [?] Disorders with hearing impairment --CHILD--> [AB51] Acquired hearing impairment Def: Loss of hearing that occurs sometime the course of life and is not present at birth. The hearing impairment is sustained after the acquisition of language, which can occur due to disease, trauma, or a... --- Walk 6 --- [AB52] Deafness not otherwise specified --PARENT--> [?] Disorders with hearing impairment --EXCLUDES--> [?] Otosclerosis Def: Otosclerosis is a genetically mediated metabolic bone disease that affects the otic capsule and stapes. It is an autosomal dominant disorder with varying penetrance and expressivity. Usually symptomat...
[ "[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....", "[4B4Z] Diseases of the immune system, unspecified\n --PARENT--> [04] Diseases of the immune system\n --CHILD--> [4A20] Acquired immunodeficiencies", "[MC1Y] Other specified symptoms or signs involving the visual system\n --PARENT--> [?] Symptoms or signs involving the visual system\n --CHILD--> [MC12] Chronic enlargement of lacrimal gland", "[MC1Y] Other specified symptoms or signs involving the visual system\n --PARENT--> [?] Symptoms or signs involving the visual system\n --CHILD--> [MC10] Eye appearance abnormal", "[AB52] Deafness not otherwise specified\n --PARENT--> [?] Disorders with hearing impairment\n --CHILD--> [AB51] Acquired hearing impairment\n Def: Loss of hearing that occurs sometime the course of life and is not present at birth. The hearing impairment is sustained after the acquisition of language, which can occur due to disease, trauma, or a...", "[AB52] Deafness not otherwise specified\n --PARENT--> [?] Disorders with hearing impairment\n --EXCLUDES--> [?] Otosclerosis\n Def: Otosclerosis is a genetically mediated metabolic bone disease that affects the otic capsule and stapes. It is an autosomal dominant disorder with varying penetrance and expressivity. Usually symptomat..." ]
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
Prior to BOR therapy, the patient was seropositive for hepatitis B surface antibody (anti-HBs) and hepatitis B core antibody (anti-HBc) with negative hepatitis B surface antigen (HBsAg), which was indicative of her having a resolved infection. Hepatitis C antibody was negative. Other laboratory values were as follows: WBC, 3000/ μ L; Hgb, 9.5 g/dL; platelets, 96,000/ μ L with normal electrolyte values. Her aminotransferase levels at that time were within normal limits [alanine aminotransferase level (ALT) 14 U/L and aspartate aminotransferase level (AST) 22 U/L]. After seroconversion, HBsAg was highly reactive with HBV DNA of 1.2 × 10 6 IU/mL (6.9 × 10 6 copies/mL); ALT was 19 U/L, AST 29 U/L, WBC 1900/ μ L, Hgb 10.8 g/dL, and platelets 142,000/ μ L. Ultrasound of the abdomen revealed an enlarged liver with coarse echo texture, which was deemed to be secondary to early cirrhosis or hepatitis. Her Naranjo adverse drug reaction probability score was 5 indicating a probable adverse drug reaction . The patient was started on tenofovir 300 mg once a week (dose adjusted for renal impairment). During the following months, she developed cancer related complications. She was admitted to the hospital with vertebral fractures requiring surgical intervention, venous thrombosis, progressive functional decline, and sepsis. She was eventually placed under comfort care and died eleven months after seroconversion.
4.015625
0.968262
sec[1]/p[2]
en
0.999998
24876846
https://doi.org/10.1155/2014/964082
[ "hepatitis", "antibody", "aminotransferase", "surface", "anti", "hbsag", "which", "platelets", "seroconversion", "adverse" ]
[ { "code": "DB97.Z", "title": "Inflammatory liver disease, unspecified" }, { "code": "1E50.Z", "title": "Acute viral hepatitis, unspecified" }, { "code": "DB97.2", "title": "Chronic hepatitis, not elsewhere classified" }, { "code": "1E5Z", "title": "Viral hepatitis, unspecified" }, { "code": "1E51.0Z", "title": "Chronic hepatitis B, unspecified" }, { "code": "JA86.Y", "title": "Maternal care for other specified fetal problems" }, { "code": "MA14.14", "title": "Anti-nuclear antibody positive" }, { "code": "MA14.13", "title": "Anti-nuclear antibody negative" }, { "code": "JA86.0", "title": "Maternal care for red cell antibodies" }, { "code": "MA14.1C", "title": "Raised antibody titre" } ]
=== ICD-11 CODES FOUND === [DB97.Z] Inflammatory liver disease, unspecified Also known as: Inflammatory liver disease, unspecified | Certain specified inflammatory liver diseases | Nonspecific reactive hepatitis | inflammatory liver disease | hepatitis NOS [1E50.Z] Acute viral hepatitis, unspecified Also known as: Acute viral hepatitis, unspecified | Acute viral hepatitis | acute anicteric hepatitis | Acute hepatitis NOS | acute viral hepatitis non-A non-B NEC [DB97.2] Chronic hepatitis, not elsewhere classified Also known as: Chronic hepatitis, not elsewhere classified | Chronic hepatitis, unspecified | Chronic active hepatitis NEC | Other specified chronic hepatitis | Chronic persistent hepatitis NEC Includes: Chronic hepatitis, unspecified | Other specified chronic hepatitis Excludes: hepatitis (chronic): granulomatous NEC | Drug-induced or toxic liver disease | hepatitis (chronic): viral [1E5Z] Viral hepatitis, unspecified Also known as: Viral hepatitis, unspecified | anicteric hepatitis [1E51.0Z] Chronic hepatitis B, unspecified Also known as: Chronic hepatitis B, unspecified | Chronic hepatitis B | Chronic hepatitis B without delta agent | chronic HBV - [hepatitis B virus] infection | hepatitis B NOS [JA86.Y] Maternal care for other specified fetal problems Also known as: Maternal care for other specified fetal problems | Maternal care for other isoimmunization | Isoimmunization NOS | maternal antibodies NOS | pregnancy management affected by incompatibility of blood groups NOS [MA14.14] Anti-nuclear antibody positive Also known as: Anti-nuclear antibody positive | ANA - [anti-nuclear antibody] positive [MA14.13] Anti-nuclear antibody negative Also known as: Anti-nuclear antibody negative | ANA - [anti-nuclear antibody] negative [JA86.0] Maternal care for red cell antibodies Definition: Maternal care for rhesus or other isoimmunization Also known as: Maternal care for red cell antibodies | Maternal care for rhesus isoimmunization | Rh factor immunization affecting management of pregnancy | Rh incompatibility | Rh incompatibility with hydrops fetalis [MA14.1C] Raised antibody titre Also known as: Raised antibody titre | antibody titre above reference range | high antibody titre | increased antibody titre Excludes: isoimmunization, in pregnancy affecting fetus or newborn === GRAPH WALKS === --- Walk 1 --- [DB97.Z] Inflammatory liver disease, unspecified --PARENT--> [DB97] Certain specified inflammatory liver diseases --EXCLUDES--> [?] Drug-induced or toxic liver disease Def: Drug-induced or toxic liver disease is hepatotoxicity as injury to the liver that is associated with impaired liver function caused by exposure to a drug or another noninfectious agent.... --- Walk 2 --- [DB97.Z] Inflammatory liver disease, unspecified --PARENT--> [DB97] Certain specified inflammatory liver diseases --EXCLUDES--> [?] Drug-induced or toxic liver disease Def: Drug-induced or toxic liver disease is hepatotoxicity as injury to the liver that is associated with impaired liver function caused by exposure to a drug or another noninfectious agent.... --- Walk 3 --- [1E50.Z] Acute viral hepatitis, unspecified --PARENT--> [1E50] Acute viral hepatitis Def: A group of liver diseases characterised by liver inflammation and fibrosis, caused by less than 6 months of infection with one or more of hepatitis B virus, hepatitis C virus and hepatitis D virus, wi... --CHILD--> [1E50.2] Acute hepatitis C Def: Acute liver injury and inflammation caused by recent and short-term (less than 6 months) infection with hepatitis C virus (HCV). Transmission is by blood and body fluid contamination (parenteral sprea... --- Walk 4 --- [1E50.Z] Acute viral hepatitis, unspecified --PARENT--> [1E50] Acute viral hepatitis Def: A group of liver diseases characterised by liver inflammation and fibrosis, caused by less than 6 months of infection with one or more of hepatitis B virus, hepatitis C virus and hepatitis D virus, wi... --RELATED_TO--> [?] Cytomegaloviral hepatitis Def: A disease of the hepatic system, caused by an infection with human cytomegalovirus. This disease is characterised by fever, acute pharyngitis, fatigue, lymphadenopathy, or jaundice. Transmission is by... --- Walk 5 --- [DB97.2] Chronic hepatitis, not elsewhere classified --EXCLUDES--> [?] Viral hepatitis Def: A group of liver diseases caused by infection with one or more of the five hepatitis viruses, hepatitis A virus, hepatitis B virus, hepatitis C virus, hepatitis D virus and hepatitis E viruses. The in... --EXCLUDES--> [?] Herpes simplex hepatitis Def: This is a viral disease caused by herpes simplex virus type 1 (HSV-1) and type 2 (HSV-2). The onset is with fever, prostration, marked elevation of transaminases and leukopenia. Acute liver failure ca... --- Walk 6 --- [DB97.2] Chronic hepatitis, not elsewhere classified --EXCLUDES--> [?] Viral hepatitis Def: A group of liver diseases caused by infection with one or more of the five hepatitis viruses, hepatitis A virus, hepatitis B virus, hepatitis C virus, hepatitis D virus and hepatitis E viruses. The in... --EXCLUDES--> [?] Non-alcoholic steatohepatitis Def: Non-alcoholic steatohepatitis (NASH) is a histological form of Non-alcoholic fatty liver disease (NAFLD) in which the key features are histological evidence of hepatocyte injury (such as ballooning or...
[ "[DB97.Z] Inflammatory liver disease, unspecified\n --PARENT--> [DB97] Certain specified inflammatory liver diseases\n --EXCLUDES--> [?] Drug-induced or toxic liver disease\n Def: Drug-induced or toxic liver disease is hepatotoxicity as injury to the liver that is associated with impaired liver function caused by exposure to a drug or another noninfectious agent....", "[DB97.Z] Inflammatory liver disease, unspecified\n --PARENT--> [DB97] Certain specified inflammatory liver diseases\n --EXCLUDES--> [?] Drug-induced or toxic liver disease\n Def: Drug-induced or toxic liver disease is hepatotoxicity as injury to the liver that is associated with impaired liver function caused by exposure to a drug or another noninfectious agent....", "[1E50.Z] Acute viral hepatitis, unspecified\n --PARENT--> [1E50] Acute viral hepatitis\n Def: A group of liver diseases characterised by liver inflammation and fibrosis, caused by less than 6 months of infection with one or more of hepatitis B virus, hepatitis C virus and hepatitis D virus, wi...\n --CHILD--> [1E50.2] Acute hepatitis C\n Def: Acute liver injury and inflammation caused by recent and short-term (less than 6 months) infection with hepatitis C virus (HCV). Transmission is by blood and body fluid contamination (parenteral sprea...", "[1E50.Z] Acute viral hepatitis, unspecified\n --PARENT--> [1E50] Acute viral hepatitis\n Def: A group of liver diseases characterised by liver inflammation and fibrosis, caused by less than 6 months of infection with one or more of hepatitis B virus, hepatitis C virus and hepatitis D virus, wi...\n --RELATED_TO--> [?] Cytomegaloviral hepatitis\n Def: A disease of the hepatic system, caused by an infection with human cytomegalovirus. This disease is characterised by fever, acute pharyngitis, fatigue, lymphadenopathy, or jaundice. Transmission is by...", "[DB97.2] Chronic hepatitis, not elsewhere classified\n --EXCLUDES--> [?] Viral hepatitis\n Def: A group of liver diseases caused by infection with one or more of the five hepatitis viruses, hepatitis A virus, hepatitis B virus, hepatitis C virus, hepatitis D virus and hepatitis E viruses. The in...\n --EXCLUDES--> [?] Herpes simplex hepatitis\n Def: This is a viral disease caused by herpes simplex virus type 1 (HSV-1) and type 2 (HSV-2). The onset is with fever, prostration, marked elevation of transaminases and leukopenia. Acute liver failure ca...", "[DB97.2] Chronic hepatitis, not elsewhere classified\n --EXCLUDES--> [?] Viral hepatitis\n Def: A group of liver diseases caused by infection with one or more of the five hepatitis viruses, hepatitis A virus, hepatitis B virus, hepatitis C virus, hepatitis D virus and hepatitis E viruses. The in...\n --EXCLUDES--> [?] Non-alcoholic steatohepatitis\n Def: Non-alcoholic steatohepatitis (NASH) is a histological form of Non-alcoholic fatty liver disease (NAFLD) in which the key features are histological evidence of hepatocyte injury (such as ballooning or..." ]
DB97.Z
Inflammatory liver disease, unspecified
[ { "from_icd11": "DB97.Z", "icd10_code": "K7581", "icd10_title": "Nonalcoholic steatohepatitis (NASH)" }, { "from_icd11": "DB97.Z", "icd10_code": "K7589", "icd10_title": "Other specified inflammatory liver diseases" }, { "from_icd11": "DB97.Z", "icd10_code": "K759", "icd10_title": "Inflammatory liver disease, unspecified" }, { "from_icd11": "DB97.Z", "icd10_code": "K752", "icd10_title": "Nonspecific reactive hepatitis" }, { "from_icd11": "DB97.Z", "icd10_code": "K75", "icd10_title": "Other inflammatory liver diseases" }, { "from_icd11": "DB97.Z", "icd10_code": "K758", "icd10_title": "Other specified inflammatory liver diseases" }, { "from_icd11": "1E50.Z", "icd10_code": "B179", "icd10_title": "Acute viral hepatitis, unspecified" }, { "from_icd11": "1E50.Z", "icd10_code": "B178", "icd10_title": "Other specified acute viral hepatitis" }, { "from_icd11": "1E50.Z", "icd10_code": "B17", "icd10_title": "Other acute viral hepatitis" }, { "from_icd11": "DB97.2", "icd10_code": "K739", "icd10_title": "Chronic hepatitis, unspecified" }, { "from_icd11": "DB97.2", "icd10_code": "K732", "icd10_title": "Chronic active hepatitis, not elsewhere classified" }, { "from_icd11": "DB97.2", "icd10_code": "K738", "icd10_title": "Other chronic hepatitis, not elsewhere classified" }, { "from_icd11": "DB97.2", "icd10_code": "K73", "icd10_title": "Chronic hepatitis, not elsewhere classified" }, { "from_icd11": "DB97.2", "icd10_code": "K730", "icd10_title": "Chronic persistent hepatitis, not elsewhere classified" }, { "from_icd11": "DB97.2", "icd10_code": "K731", "icd10_title": "Chronic lobular hepatitis, not elsewhere classified" } ]
K7581
Nonalcoholic steatohepatitis (NASH)
A 63-year-old man presented with two days' digestive symptoms: nausea, vomiting, diarrhea, and abdominal pain with fever and asthenia. The patient had a history of hypertension (treated with amlodipine), chronic lymphocytic leukemia stage A with a monoclonal gamma peak, and septic shock in 2012. Six month earlier, a routine blood sample analysis showed no abnormality with the notable exception of a peak of gammaglobulins (16,4 g/L). At his home, the paramedical team found high blood pressure and oxygen saturation and a heart rate of 102 per minute in a pale patient, sweating and asthenic, and no neurological disorder. He had abdominal pain without tenderness, nausea, and hypothermia at 33.8°C. He showed no chest pain, no signs of heart failure, and no radial pulse, and his veins of the lower limbs and abdomen were apparent. He had a pulmonary surface polypnea at 34 per minute and cyanosis of the extremities (SpO 2 84%), but normal auscultation. HemoCue was at 23.6 g/dL and glucose was at 1.7 g/L. Proteinuria was negative on a urinal quick test, the protein was 43 g/L, and glomerular renal filtration was found at 30 mL/min. Albumin was at 24.7 g/L and all blood immunoglobulins were low. Concerning liver laboratory findings, only gamma GT was 3 times higher than normal. The electrocardiogram revealed a sinus rhythm at 100 per minute with a narrow QRS without conduction disturbance or repolarization.
3.919922
0.983398
sec[1]/p[0]
en
0.999997
27069700
https://doi.org/10.1155/2016/5347039
[ "pain", "blood", "minute", "nausea", "abdominal", "gamma", "peak", "heart", "without", "digestive" ]
[ { "code": "MG3Z", "title": "Pain, unspecified" }, { "code": "8E43.Z", "title": "Pain disorders, unspecified" }, { "code": "MG31.Z", "title": "Acute pain, unspecified" }, { "code": "MG30.Z", "title": "Chronic pain, unspecified" }, { "code": "FB56.2", "title": "Myalgia" }, { "code": "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 === [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 [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 --- [MG3Z] Pain, unspecified --PARENT--> [?] Pain --CHILD--> [MG30] Chronic pain Def: Pain is an unpleasant sensory and emotional experience associated with, or resembling that associated with, actual or potential tissue damage. Chronic pain is pain that persists or recurs for longer t... --- Walk 2 --- [MG3Z] Pain, unspecified --PARENT--> [?] Pain --EXCLUDES--> [?] Mastodynia Def: The symptom of breast pain. This symptom may be classified as cyclic or non-cyclical depending on the clinical patterns.... --- Walk 3 --- [8E43.Z] Pain disorders, unspecified --PARENT--> [8E43] Pain disorders --CHILD--> [8E43.Y] Other specified pain disorders --- Walk 4 --- [8E43.Z] Pain disorders, unspecified --PARENT--> [8E43] Pain disorders --CHILD--> [8E43.Z] Pain disorders, unspecified --- Walk 5 --- [MG31.Z] Acute pain, unspecified --PARENT--> [MG31] Acute pain Def: Pain with a duration of less than 3 months. This code should be used only when there is no further specification of site.... --CHILD--> [MG31.0] Acute pain in the face, not elsewhere classified --- Walk 6 --- [MG31.Z] Acute pain, unspecified --PARENT--> [MG31] Acute pain Def: Pain with a duration of less than 3 months. This code should be used only when there is no further specification of site.... --CHILD--> [MG31.1] Acute headache, not elsewhere classified
[ "[MG3Z] Pain, unspecified\n --PARENT--> [?] Pain\n --CHILD--> [MG30] Chronic pain\n Def: Pain is an unpleasant sensory and emotional experience associated with, or resembling that associated with, actual or potential tissue damage. Chronic pain is pain that persists or recurs for longer t...", "[MG3Z] Pain, unspecified\n --PARENT--> [?] Pain\n --EXCLUDES--> [?] Mastodynia\n Def: The symptom of breast pain. This symptom may be classified as cyclic or non-cyclical depending on the clinical patterns....", "[8E43.Z] Pain disorders, unspecified\n --PARENT--> [8E43] Pain disorders\n --CHILD--> [8E43.Y] Other specified pain disorders", "[8E43.Z] Pain disorders, unspecified\n --PARENT--> [8E43] Pain disorders\n --CHILD--> [8E43.Z] Pain disorders, unspecified", "[MG31.Z] Acute pain, unspecified\n --PARENT--> [MG31] Acute pain\n Def: Pain with a duration of less than 3 months.\n\nThis code should be used only when there is no further specification of site....\n --CHILD--> [MG31.0] Acute pain in the face, not elsewhere classified", "[MG31.Z] Acute pain, unspecified\n --PARENT--> [MG31] Acute pain\n Def: Pain with a duration of less than 3 months.\n\nThis code should be used only when there is no further specification of site....\n --CHILD--> [MG31.1] Acute headache, not elsewhere classified" ]
MG3Z
Pain, unspecified
[ { "from_icd11": "MG3Z", "icd10_code": "R52", "icd10_title": "Pain, unspecified" }, { "from_icd11": "MG3Z", "icd10_code": "R529", "icd10_title": "" }, { "from_icd11": "MG31.Z", "icd10_code": "R520", "icd10_title": "" }, { "from_icd11": "MG30.Z", "icd10_code": "R521", "icd10_title": "" }, { "from_icd11": "MG30.Z", "icd10_code": "R522", "icd10_title": "" }, { "from_icd11": "FB56.2", "icd10_code": "M7918", "icd10_title": "Myalgia, other site" }, { "from_icd11": "FB56.2", "icd10_code": "M7910", "icd10_title": "Myalgia, unspecified site" }, { "from_icd11": "FB56.2", "icd10_code": "M7912", "icd10_title": "Myalgia of auxiliary muscles, head and neck" }, { "from_icd11": "FB56.2", "icd10_code": "M791", "icd10_title": "Myalgia" }, { "from_icd11": "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" } ]
R52
Pain, unspecified
All patients presenting to the ED with facial pain, especially if it is new in onset or different from previous episodes, should have a thorough physical exam including complete neurological and ophthalmological exam, with specific focus on cranial nerve deficits and intraocular pressures. Any abnormalities on this exam should prompt the provider to strongly consider further investigation with neuroimaging, as they are potentially caused by a life-threatening intracranial process such as a large PCOM aneurysm. In this case, a detailed neurologic exam was performed, but irritation of the trigeminal nerve was attributed to a peripheral cause instead of a central cause. In this patient’s case, it appears that her trigeminal neuralgia was caused by a central irritation due to the compression by the bilobed aneurysm. This is likely why her pain (and CN III deficit) resolved after surgery. If neuroimaging is not pursued during the patient’s ED visit (as it was not in this patient’s first visit due to lack of perceived central neurological deficits), it is imperative that strict ED return precautions be given. These should include neurological deficits such as vision or eye movement deterioration as well as worsening of the patient’s pain. As in this case, such return precautions can lead to timely reevaluation of the patient, where changes in physical exam can be identified and further workup performed.
4.027344
0.699219
sec[2]/p[1]
en
0.999997
27833694
https://doi.org/10.5811/westjem.2016.8.30457
[ "this", "exam", "pain", "neurological", "deficits", "physical", "nerve", "neuroimaging", "caused", "aneurysm" ]
[ { "code": "4A01.03", "title": "Transient hypogammaglobulinaemia of infancy" }, { "code": "6B03", "title": "Specific phobia" }, { "code": "MG3Z", "title": "Pain, unspecified" }, { "code": "8E43.Z", "title": "Pain disorders, unspecified" }, { "code": "MG31.Z", "title": "Acute pain, unspecified" }, { "code": "MG30.Z", "title": "Chronic pain, unspecified" }, { "code": "FB56.2", "title": "Myalgia" }, { "code": "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" } ]
=== ICD-11 CODES FOUND === [4A01.03] Transient hypogammaglobulinaemia of infancy Also known as: Transient hypogammaglobulinaemia of infancy | immunoglobulin maturational delay | THI - [transient hypogammaglobulinaemia of infancy] [6B03] Specific phobia Definition: Specific phobia is characterised by a marked and excessive fear or anxiety that consistently occurs upon exposure or anticipation of exposure to one or more specific objects or situations (e.g., proximity to certain animals, flying, heights, closed spaces, sight of blood or injury) that is out of proportion to actual danger. The phobic objects or situations are avoided or else endured with intense fear or anxiety. Symptoms persist for at least several months and are sufficiently severe to result Also known as: Specific phobia | Simple phobia | isolated phobia | Acarophobia | Acrophobia Includes: Simple phobia Excludes: Body dysmorphic disorder | Hypochondriasis [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 [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 === GRAPH WALKS === --- Walk 1 --- [4A01.03] Transient hypogammaglobulinaemia of infancy --PARENT--> [4A01.0] Immunodeficiencies with predominantly antibody defects Def: A disorder characterised by an inability to mount a normal immune response due to antibody (i.e. immunoglobulin) defects... --CHILD--> [4A01.01] Immunodeficiencies with severe reduction in at least two serum immunoglobulin isotypes with normal or low numbers of B cells Def: This refers to a nonfamilial type of primary immune deficiency disease characterised by a reduction in at least two serum immunoglobulin isotypes. Circulating B cells may be normal or low.... --- Walk 2 --- [4A01.03] Transient hypogammaglobulinaemia of infancy --PARENT--> [4A01.0] Immunodeficiencies with predominantly antibody defects Def: A disorder characterised by an inability to mount a normal immune response due to antibody (i.e. immunoglobulin) defects... --CHILD--> [4A01.00] Hereditary agammaglobulinaemia with profoundly reduced or absent B cells Def: This refers to a hereditary type of primary immune deficiency disease characterised by a reduction in all types of gamma globulins, and rare X-linked genetic disorder that affects the body's ability t... --- Walk 3 --- [6B03] Specific phobia Def: Specific phobia is characterised by a marked and excessive fear or anxiety that consistently occurs upon exposure or anticipation of exposure to one or more specific objects or situations (e.g., proxi... --EXCLUDES--> [?] Body dysmorphic disorder Def: Body Dysmorphic Disorder is characterised by persistent preoccupation with one or more perceived defects or flaws in appearance that are either unnoticeable or only slightly noticeable to others. Indi... --EXCLUDES--> [?] Concern about body appearance --- Walk 4 --- [6B03] Specific phobia Def: Specific phobia is characterised by a marked and excessive fear or anxiety that consistently occurs upon exposure or anticipation of exposure to one or more specific objects or situations (e.g., proxi... --EXCLUDES--> [?] Body dysmorphic disorder Def: Body Dysmorphic Disorder is characterised by persistent preoccupation with one or more perceived defects or flaws in appearance that are either unnoticeable or only slightly noticeable to others. Indi... --EXCLUDES--> [?] Anorexia Nervosa Def: Anorexia Nervosa is characterised by significantly low body weight for the individual’s height, age and developmental stage that is not due to another health condition or to the unavailability of food... --- Walk 5 --- [MG3Z] Pain, unspecified --PARENT--> [?] Pain --EXCLUDES--> [?] Headache disorders --- Walk 6 --- [MG3Z] Pain, unspecified --PARENT--> [?] Pain --EXCLUDES--> [?] Headache disorders
[ "[4A01.03] Transient hypogammaglobulinaemia of infancy\n --PARENT--> [4A01.0] Immunodeficiencies with predominantly antibody defects\n Def: A disorder characterised by an inability to mount a normal immune response due to antibody (i.e. immunoglobulin) defects...\n --CHILD--> [4A01.01] Immunodeficiencies with severe reduction in at least two serum immunoglobulin isotypes with normal or low numbers of B cells\n Def: This refers to a nonfamilial type of primary immune deficiency disease characterised by a reduction in at least two serum immunoglobulin isotypes. Circulating B cells may be normal or low....", "[4A01.03] Transient hypogammaglobulinaemia of infancy\n --PARENT--> [4A01.0] Immunodeficiencies with predominantly antibody defects\n Def: A disorder characterised by an inability to mount a normal immune response due to antibody (i.e. immunoglobulin) defects...\n --CHILD--> [4A01.00] Hereditary agammaglobulinaemia with profoundly reduced or absent B cells\n Def: This refers to a hereditary type of primary immune deficiency disease characterised by a reduction in all types of gamma globulins, and rare X-linked genetic disorder that affects the body's ability t...", "[6B03] Specific phobia\n Def: Specific phobia is characterised by a marked and excessive fear or anxiety that consistently occurs upon exposure or anticipation of exposure to one or more specific objects or situations (e.g., proxi...\n --EXCLUDES--> [?] Body dysmorphic disorder\n Def: Body Dysmorphic Disorder is characterised by persistent preoccupation with one or more perceived defects or flaws in appearance that are either unnoticeable or only slightly noticeable to others. Indi...\n --EXCLUDES--> [?] Concern about body appearance", "[6B03] Specific phobia\n Def: Specific phobia is characterised by a marked and excessive fear or anxiety that consistently occurs upon exposure or anticipation of exposure to one or more specific objects or situations (e.g., proxi...\n --EXCLUDES--> [?] Body dysmorphic disorder\n Def: Body Dysmorphic Disorder is characterised by persistent preoccupation with one or more perceived defects or flaws in appearance that are either unnoticeable or only slightly noticeable to others. Indi...\n --EXCLUDES--> [?] Anorexia Nervosa\n Def: Anorexia Nervosa is characterised by significantly low body weight for the individual’s height, age and developmental stage that is not due to another health condition or to the unavailability of food...", "[MG3Z] Pain, unspecified\n --PARENT--> [?] Pain\n --EXCLUDES--> [?] Headache disorders", "[MG3Z] Pain, unspecified\n --PARENT--> [?] Pain\n --EXCLUDES--> [?] Headache disorders" ]
4A01.03
Transient hypogammaglobulinaemia of infancy
[ { "from_icd11": "4A01.03", "icd10_code": "D807", "icd10_title": "Transient hypogammaglobulinemia of infancy" }, { "from_icd11": "6B03", "icd10_code": "F40240", "icd10_title": "Claustrophobia" }, { "from_icd11": "6B03", "icd10_code": "F40231", "icd10_title": "Fear of injections and transfusions" }, { "from_icd11": "6B03", "icd10_code": "F40210", "icd10_title": "Arachnophobia" }, { "from_icd11": "6B03", "icd10_code": "F40243", "icd10_title": "Fear of flying" }, { "from_icd11": "6B03", "icd10_code": "F40241", "icd10_title": "Acrophobia" }, { "from_icd11": "6B03", "icd10_code": "F40232", "icd10_title": "Fear of other medical care" }, { "from_icd11": "6B03", "icd10_code": "F40298", "icd10_title": "Other specified phobia" }, { "from_icd11": "6B03", "icd10_code": "F40218", "icd10_title": "Other animal type phobia" }, { "from_icd11": "6B03", "icd10_code": "F402", "icd10_title": "Specific (isolated) phobias" }, { "from_icd11": "MG3Z", "icd10_code": "R52", "icd10_title": "Pain, unspecified" }, { "from_icd11": "MG3Z", "icd10_code": "R529", "icd10_title": "" }, { "from_icd11": "MG31.Z", "icd10_code": "R520", "icd10_title": "" }, { "from_icd11": "MG30.Z", "icd10_code": "R521", "icd10_title": "" }, { "from_icd11": "MG30.Z", "icd10_code": "R522", "icd10_title": "" } ]
D807
Transient hypogammaglobulinemia of infancy
Cases #10 and #11 were similar to the 8th case, in that they had received no cardiac treatment or follow-up. Neither received cardiologist or obstetrician care during this pregnancy. Case #10 had one vaginal delivery four years earlier, in which the baby died due to prematurity. Case #11 had one CS seven years earlier and that baby is alive without any abnormality. In addition, Case #11 had one induction six years earlier at 17 gestational weeks for FD, and two abortions. They were admitted into our hospital respectively at 34 and 33 +4 gestational weeks for heart failure with severe PAH. Upon admission, they were both found to have large VSD’s and had progressed to ES. The ECG of Case #10 after admission showed sinus rhythm with left bundle branch block and left axis deviation (−62 ° ), suggesting left atrial enlargement and right ventricular hypertrophy. The ECG of Case #11 showed sinus rhythm, complete right bundle branch block with first degree atrioventricular block, right ventricular hypertrophy and left atrial enlargement. Emergency CS under general anesthesia was performed on the day of admission in both patients because of labor. After delivery, to treat severe pulmonary infection and heart failure, both mothers were supported with ventilators. However, both died three days after operation. Post-mortem examination was refused. Their babies both survived without any abnormal manifestation.
3.9375
0.973145
sec[2]/sec[3]/p[4]
en
0.999995
27852228
https://doi.org/10.1186/s12884-016-1153-z
[ "both", "they", "block", "that", "delivery", "baby", "died", "without", "gestational", "heart" ]
[ { "code": "LB99.6", "title": "Acheiria" }, { "code": "MB51.Z", "title": "Diplegia of upper extremities, unspecified" }, { "code": "LB9A.4", "title": "Apodia" }, { "code": "LB51", "title": "Anorchia or microorchidia" }, { "code": "9D90.2", "title": "Moderate vision impairment" }, { "code": "GB6Z", "title": "Kidney failure, unspecified" }, { "code": "DB98.3", "title": "Portal vein thrombosis" }, { "code": "FA34.4", "title": "Ankylosis of joint" }, { "code": "BC63.2Z", "title": "Complete atrioventricular block, unspecified" }, { "code": "DB98.5", "title": "Budd-Chiari syndrome" } ]
=== ICD-11 CODES FOUND === [LB99.6] Acheiria Definition: A condition caused by failure of one or both hands to develop during the antenatal period. Also known as: Acheiria | Congenital absence of hand | agenesis of hand | congenital absence of hand and finger | congenital absence of hand and wrist [MB51.Z] Diplegia of upper extremities, unspecified Also known as: Diplegia of upper extremities, unspecified | Diplegia of upper extremities | paralysis of both upper limbs | both upper extremity paralysis | diplegia of upper limbs [LB9A.4] Apodia Definition: A condition caused by failure of the foot to develop during the antenatal period. Also known as: Apodia | Congenital absence of foot | agenesis of foot | congenital absence of foot or toe | congenital absence of foot or toe, unspecified side [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 [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 [GB6Z] Kidney failure, unspecified Also known as: Kidney failure, unspecified | nontraumatic kidney injury | renal failure NOS | kidney block | renal impairment NOS [DB98.3] Portal vein thrombosis Definition: Portal vein thrombosis is a condition where the portal vein and/or its branches are obstructed, mainly by a blood clot or malignant tumour invasion. Also known as: Portal vein thrombosis | Phlebitis of portal vein | deep vein thrombosis of portal vein | portal thrombosis | PVT - [portal vein thrombosis] Includes: Phlebitis of portal vein [FA34.4] Ankylosis of joint Definition: The term ankylosis denotes restricted movement in the joint, and it can be bony or fibrous. Most cases are caused by trauma, infection, radiotherapy, or severe arthritic condition. Also known as: Ankylosis of joint | ankylosis | ankylosis of joint, site unspecified | frozen joint | fusion of joint Excludes: stiffness of joint without ankylosis | Ankylosis of spinal joint [BC63.2Z] Complete atrioventricular block, unspecified Also known as: Complete atrioventricular block, unspecified | Complete atrioventricular block | Third-degree block | complete atrioventricular heart block | complete heart block [DB98.5] Budd-Chiari syndrome Definition: Budd-Chiari syndrome (BCS) is caused by obstruction of hepatic venous outflow involving either the hepatic veins or the terminal segment of the inferior vena cava and leading to hepatic congestion and ischemic necrosis. Severity depends on the speed of onset and extent of the obstruction. Obstructions are generally caused by thrombosis in primary BCS, while secondary BCS results from tumour invasion into the lumen or compression of the vein by an expansive lesion. The principle manifestations o Also known as: Budd-Chiari syndrome | hepatic vein block | obstruction of hepatic veins | Chiari syndrome | hepatic vein obstruction === GRAPH WALKS === --- Walk 1 --- [LB99.6] Acheiria Def: A condition caused by failure of one or both hands to develop during the antenatal period.... --PARENT--> [LB99] Reduction defects of upper limb Def: Any condition caused by the failure of an upper limb to correctly develop during the antenatal period. These conditions are characterised by reduction in size or absence of the limb.... --CHILD--> [LB99.0] Amelia of upper limb Def: A condition caused by the failure of an upper limb to develop during the antenatal period. This condition is characterised by absence of the upper limb.... --- Walk 2 --- [LB99.6] Acheiria Def: A condition caused by failure of one or both hands to develop during the antenatal period.... --PARENT--> [LB99] Reduction defects of upper limb Def: Any condition caused by the failure of an upper limb to correctly develop during the antenatal period. These conditions are characterised by reduction in size or absence of the limb.... --CHILD--> [LB99.1] Humeral agenesis or hypoplasia --- Walk 3 --- [MB51.Z] Diplegia of upper extremities, unspecified --PARENT--> [MB51] Diplegia of upper extremities Def: This is a loss of motor control in both arms.... --CHILD--> [MB51.0] Flaccid diplegia of upper extremities --- Walk 4 --- [MB51.Z] Diplegia of upper extremities, unspecified --PARENT--> [MB51] Diplegia of upper extremities Def: This is a loss of motor control in both arms.... --CHILD--> [MB51.Z] Diplegia of upper extremities, unspecified --- Walk 5 --- [LB9A.4] Apodia Def: A condition caused by failure of the foot to develop during the antenatal period.... --PARENT--> [LB9A] Reduction defects of lower limb Def: Any condition caused by the failure of a lower limb to correctly develop during the antenatal period. These conditions are characterised by reduction in size or absence of the limb.... --CHILD--> [LB9A.2] Fibular hemimelia Def: Fibular hemimelia is a congenital longitudinal limb deficiency characterised by complete or partial absence of the fibula bone.... --- Walk 6 --- [LB9A.4] Apodia Def: A condition caused by failure of the foot to develop during the antenatal period.... --PARENT--> [LB9A] Reduction defects of lower limb Def: Any condition caused by the failure of a lower limb to correctly develop during the antenatal period. These conditions are characterised by reduction in size or absence of the limb.... --CHILD--> [LB9A.0] Amelia of lower limb
[ "[LB99.6] Acheiria\n Def: A condition caused by failure of one or both hands to develop during the antenatal period....\n --PARENT--> [LB99] Reduction defects of upper limb\n Def: Any condition caused by the failure of an upper limb to correctly develop during the antenatal period. These conditions are characterised by reduction in size or absence of the limb....\n --CHILD--> [LB99.0] Amelia of upper limb\n Def: A condition caused by the failure of an upper limb to develop during the antenatal period. This condition is characterised by absence of the upper limb....", "[LB99.6] Acheiria\n Def: A condition caused by failure of one or both hands to develop during the antenatal period....\n --PARENT--> [LB99] Reduction defects of upper limb\n Def: Any condition caused by the failure of an upper limb to correctly develop during the antenatal period. These conditions are characterised by reduction in size or absence of the limb....\n --CHILD--> [LB99.1] Humeral agenesis or hypoplasia", "[MB51.Z] Diplegia of upper extremities, unspecified\n --PARENT--> [MB51] Diplegia of upper extremities\n Def: This is a loss of motor control in both arms....\n --CHILD--> [MB51.0] Flaccid diplegia of upper extremities", "[MB51.Z] Diplegia of upper extremities, unspecified\n --PARENT--> [MB51] Diplegia of upper extremities\n Def: This is a loss of motor control in both arms....\n --CHILD--> [MB51.Z] Diplegia of upper extremities, unspecified", "[LB9A.4] Apodia\n Def: A condition caused by failure of the foot to develop during the antenatal period....\n --PARENT--> [LB9A] Reduction defects of lower limb\n Def: Any condition caused by the failure of a lower limb to correctly develop during the antenatal period. These conditions are characterised by reduction in size or absence of the limb....\n --CHILD--> [LB9A.2] Fibular hemimelia\n Def: Fibular hemimelia is a congenital longitudinal limb deficiency characterised by complete or partial absence of the fibula bone....", "[LB9A.4] Apodia\n Def: A condition caused by failure of the foot to develop during the antenatal period....\n --PARENT--> [LB9A] Reduction defects of lower limb\n Def: Any condition caused by the failure of a lower limb to correctly develop during the antenatal period. These conditions are characterised by reduction in size or absence of the limb....\n --CHILD--> [LB9A.0] Amelia of lower limb" ]
LB99.6
Acheiria
[ { "from_icd11": "LB99.6", "icd10_code": "Q7131", "icd10_title": "Congenital absence of right hand and finger" }, { "from_icd11": "LB99.6", "icd10_code": "Q7133", "icd10_title": "Congenital absence of hand and finger, bilateral" }, { "from_icd11": "LB99.6", "icd10_code": "Q7130", "icd10_title": "Congenital absence of unspecified hand and finger" }, { "from_icd11": "LB99.6", "icd10_code": "Q713", "icd10_title": "Congenital absence of hand and finger" }, { "from_icd11": "MB51.Z", "icd10_code": "G830", "icd10_title": "Diplegia of upper limbs" }, { "from_icd11": "LB9A.4", "icd10_code": "Q7231", "icd10_title": "Congenital absence of right foot and toe(s)" }, { "from_icd11": "LB9A.4", "icd10_code": "Q7230", "icd10_title": "Congenital absence of unspecified foot and toe(s)" }, { "from_icd11": "LB9A.4", "icd10_code": "Q723", "icd10_title": "Congenital absence of foot and toe(s)" }, { "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": "9D90.2", "icd10_code": "H542", "icd10_title": "Low vision, both eyes" }, { "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": "DB98.3", "icd10_code": "I81", "icd10_title": "Portal vein thrombosis" } ]
Q7131
Congenital absence of right hand and finger
A 10-day-old female baby was born at term with a spontaneous delivery without any complications. Mother was G2, P1; her first pregnancy was a loss resulting from an ectopic pregnancy. The birth weight of baby was 8 lb. Both prenatal and post-natal courses were normal. The infant was fed with breast milk for 10–15 min from each breast every 2–3 h. However, the patient was observed by her pediatrician and noted to be underweight during the well-baby checkup at day 7 after birth. At that time, the mother complained that the baby was feeding poorly; however, on physical examination there were no signs of virilization and the external genitalia was normal for a female. After three days, she presented to the emergency department with difficulty in breathing and lethargy. Her documented weight in the emergency room was 7 lb. The patient was noted to have bradycardia, heart rate 63/min, and blood pressure of 41/30 mmHg. She was given epinephrine and placed on a dopamine drip. Then she was intubated and an ECG revealed elevated T wave and a wide QRS complex. With regard to her family history, the patient has no siblings. The parents are separated and her father lives in a different country. The mother states that the baby's father had episodes of dehydration and liked eating salt; however, the father is healthy and has no obvious medical problem to her knowledge. The mother remains completely asymptomatic.
3.580078
0.988281
sec[1]/p[0]
en
0.999996
24688761
https://doi.org/10.1530/EDM-13-0077
[ "baby", "mother", "however", "that", "father", "pregnancy", "birth", "weight", "breast", "emergency" ]
[ { "code": "6E20", "title": "Mental or behavioural disorders associated with pregnancy, childbirth or the puerperium, without psychotic symptoms" }, { "code": "KD34", "title": "Reactions or intoxications due to drugs administered to fetus or newborn" }, { "code": "KB08.2", "title": "Congenital hypotonia" }, { "code": "LD90.Y", "title": "Other specified conditions with disorders of intellectual development as a relevant clinical feature" }, { "code": "EC20.02", "title": "Autosomal recessive congenital ichthyosis" }, { "code": "QA48.1", "title": "Care or examination of lactating mother" }, { "code": "KB60.1", "title": "Syndrome of infant of a diabetic mother, type 1 or 2, nongestational, insulin dependent" }, { "code": "1C1D.0", "title": "Primary yaws" }, { "code": "KD35", "title": "Neonatal withdrawal syndrome from maternal use of drugs of addiction" }, { "code": "KB60.0", "title": "Syndrome of infant of mother with gestational diabetes" } ]
=== ICD-11 CODES FOUND === [6E20] Mental or behavioural disorders associated with pregnancy, childbirth or the puerperium, without psychotic symptoms Definition: A syndrome associated with pregnancy or the puerperium (commencing within about 6 weeks after delivery) that involves significant mental and behavioural features, most commonly depressive symptoms. The syndrome does not include delusions, hallucinations, or other psychotic symptoms. If the symptoms meet the diagnostic requirements for a specific mental disorder, that diagnosis should also be assigned. This designation should not be used to describe mild and transient depressive symptoms that do Also known as: Mental or behavioural disorders associated with pregnancy, childbirth or the puerperium, without psychotic symptoms | mental or behavioural disorders associated with pregnancy, childbirth or the puerperium, without psychotic features | Postpartum depression NOS | postnatal depression NOS | puerperal depression NOS [KD34] Reactions or intoxications due to drugs administered to fetus or newborn Definition: A group of paediatric substance-induced conditions associated with health interventions applied to a fetus or newborn using pharmaceutical products. Also known as: Reactions or intoxications due to drugs administered to fetus or newborn | newborn drug intoxication | Chloramphenicol toxicity in the newborn | Grey baby syndrome | Grey baby Excludes: Withdrawal symptoms from therapeutic use of drugs in newborn | Neonatal hyperbilirubinaemia due to drugs or toxins transmitted from mother | reactions and intoxications from maternal opiates, tranquillizers and other medication [KB08.2] Congenital hypotonia Definition: A paediatric condition characterised by abnormally decreased muscle tone that is present at birth in a newborn. Also known as: Congenital hypotonia | floppy baby | floppy baby syndrome | floppy infant | floppy infant syndrome Includes: Nonspecific floppy baby syndrome [LD90.Y] Other specified conditions with disorders of intellectual development as a relevant clinical feature Also known as: Other specified conditions with disorders of intellectual development as a relevant clinical feature | Non-syndromic conditions with disorders of intellectual development as a relevant clinical feature | Autosomal dominant non-syndromic intellectual deficit | Autosomal recessive non-syndromic intellectual deficit | X-linked non-syndromic intellectual deficit [EC20.02] Autosomal recessive congenital ichthyosis Definition: A heterogeneous group of genetically-determined ichthyoses with autosomal recessive inheritance. Also known as: Autosomal recessive congenital ichthyosis | Congenital non-bullous ichthyosiform erythroderma | Congenital ichthyotic ichthyosis | Lamellar ichthyosis | Collodion baby [QA48.1] Care or examination of lactating mother Also known as: Care or examination of lactating mother | care of lactating mother | examination of lactating mother | supervision of lactation | supervision of breastfeeding Excludes: Certain specified disorders of breast or lactation associated with childbirth [KB60.1] Syndrome of infant of a diabetic mother, type 1 or 2, nongestational, insulin dependent Definition: 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, birth injuries, congenital anomalies, hypoglycaemia, respiratory distress, caudal regression syndrome and hypertrophic cardiomyopathy. Also known as: Syndrome of infant of a diabetic mother, type 1 or 2, nongestational, insulin dependent | infant of a diabetic mother syndrome | maternal diabetes syndrome | syndrome of infant of diabetic mother | infant of diabetic mother [1C1D.0] Primary yaws Definition: Primary yaws results from primary inoculation of Treponema pallidum subsp. pertenue into the skin, manifesting 2-12 weeks later as a localised papule (initial, primary or ‘mother' yaw) before developing into a large non-tender ulcerating nodule, often resembling a raspberry (hence the name ‘framboesia’). The primary lesion is most commonly located on the legs and ankles may also be found on the buttocks, arms, hands, and face. It usually heals after 3–6 months and is still present at the onset o Also known as: Primary yaws | Chancre of yaws | Primary framboesia | initial lesions of yaws | mother yaw Includes: Chancre of yaws | Primary framboesia [KD35] Neonatal withdrawal syndrome from maternal use of drugs of addiction Definition: Intrauterine exposure to addictive drugs can lead to neonatal withdrawal symptoms. Withdrawal symptoms are usually neurological, preventing normal autonomic function. The clinical presentation of drug withdrawal is variable and dependent on several factors, such as, the type and dose of drug used and rate of metabolism and excretion of the mother and infant. Also known as: Neonatal withdrawal syndrome from maternal use of drugs of addiction | Drug withdrawal syndrome in infant of dependent mother | Neonatal abstinence syndrome | drug withdrawal syndrome in newborn | neonatal drug withdrawal syndrome Includes: Drug withdrawal syndrome in infant of dependent mother | Neonatal abstinence syndrome Excludes: Fetus or newborn affected by maternal anaesthesia or analgesia in pregnancy, labour or delivery [KB60.0] Syndrome of infant of mother with gestational diabetes Definition: 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 effects include macrosomia, intrauterine growth restriction, birth injuries, congenital anomalies, hypoglycaemia, respiratory distress, and hypertrophic cardiomyopathy. Also known as: Syndrome of infant of mother with gestational diabetes | infant of mother with gestational diabetes | IGDM - [infant of gestational diabetic mother] | Fetus or newborn with hypoglycaemia affected by maternal gestational diabetes | Fetus or newborn affected by maternal gestational diabetes === GRAPH WALKS === --- Walk 1 --- [6E20] Mental or behavioural disorders associated with pregnancy, childbirth or the puerperium, without psychotic symptoms Def: A syndrome associated with pregnancy or the puerperium (commencing within about 6 weeks after delivery) that involves significant mental and behavioural features, most commonly depressive symptoms. Th... --PARENT--> [?] Mental or behavioural disorders associated with pregnancy, childbirth or the puerperium Def: Syndromes associated with pregnancy or the puerperium (commencing within about 6 weeks after delivery) that involve significant mental and behavioural features. If the symptoms meet the diagnostic req... --CHILD--> [6E2Z] Mental or behavioural disorders associated with pregnancy, childbirth or the puerperium, unspecified --- Walk 2 --- [6E20] Mental or behavioural disorders associated with pregnancy, childbirth or the puerperium, without psychotic symptoms Def: A syndrome associated with pregnancy or the puerperium (commencing within about 6 weeks after delivery) that involves significant mental and behavioural features, most commonly depressive symptoms. Th... --PARENT--> [?] Mental or behavioural disorders associated with pregnancy, childbirth or the puerperium Def: Syndromes associated with pregnancy or the puerperium (commencing within about 6 weeks after delivery) that involve significant mental and behavioural features. If the symptoms meet the diagnostic req... --CHILD--> [6E2Z] Mental or behavioural disorders associated with pregnancy, childbirth or the puerperium, unspecified --- Walk 3 --- [KD34] Reactions or intoxications due to drugs administered to fetus or newborn Def: A group of paediatric substance-induced conditions associated with health interventions applied to a fetus or newborn using pharmaceutical products.... --EXCLUDES--> [?] Withdrawal symptoms from therapeutic use of drugs in newborn Def: A paediatric condition characterised by the presence of symptoms due to drug withdrawal in a newborn.... --PARENT--> [?] Certain disorders originating in the perinatal period Def: A group of any other paediatric conditions that occur during the period of time around childbirth, especially the five months before and one month after birth.... --- Walk 4 --- [KD34] Reactions or intoxications due to drugs administered to fetus or newborn Def: A group of paediatric substance-induced conditions associated with health interventions applied to a fetus or newborn using pharmaceutical products.... --EXCLUDES--> [?] Neonatal hyperbilirubinaemia due to drugs or toxins transmitted from mother --PARENT--> [?] Neonatal hyperbilirubinaemia due to drugs or toxins Def: A condition characterised as an increased level of bilirubin above 85 umol/l (5 mg/dL) which manifests as yellowing of the eyes, skin, and other tissues of a newborn due to the transmission of any dru... --- Walk 5 --- [KB08.2] Congenital hypotonia Def: A paediatric condition characterised by abnormally decreased muscle tone that is present at birth in a newborn.... --PARENT--> [KB08] Disorders of muscle tone of newborn Def: A group of paediatric conditions characterised by abnormal muscle tone in a newborn.... --PARENT--> [?] Neurological disorders specific to the perinatal or neonatal period Def: A group of paediatric conditions characterised by an abnormal change in the cerebral status of a newborn.... --- Walk 6 --- [KB08.2] Congenital hypotonia Def: A paediatric condition characterised by abnormally decreased muscle tone that is present at birth in a newborn.... --PARENT--> [KB08] Disorders of muscle tone of newborn Def: A group of paediatric conditions characterised by abnormal muscle tone in a newborn.... --CHILD--> [KB08.2] Congenital hypotonia Def: A paediatric condition characterised by abnormally decreased muscle tone that is present at birth in a newborn....
[ "[6E20] Mental or behavioural disorders associated with pregnancy, childbirth or the puerperium, without psychotic symptoms\n Def: A syndrome associated with pregnancy or the puerperium (commencing within about 6 weeks after delivery) that involves significant mental and behavioural features, most commonly depressive symptoms. Th...\n --PARENT--> [?] Mental or behavioural disorders associated with pregnancy, childbirth or the puerperium\n Def: Syndromes associated with pregnancy or the puerperium (commencing within about 6 weeks after delivery) that involve significant mental and behavioural features. If the symptoms meet the diagnostic req...\n --CHILD--> [6E2Z] Mental or behavioural disorders associated with pregnancy, childbirth or the puerperium, unspecified", "[6E20] Mental or behavioural disorders associated with pregnancy, childbirth or the puerperium, without psychotic symptoms\n Def: A syndrome associated with pregnancy or the puerperium (commencing within about 6 weeks after delivery) that involves significant mental and behavioural features, most commonly depressive symptoms. Th...\n --PARENT--> [?] Mental or behavioural disorders associated with pregnancy, childbirth or the puerperium\n Def: Syndromes associated with pregnancy or the puerperium (commencing within about 6 weeks after delivery) that involve significant mental and behavioural features. If the symptoms meet the diagnostic req...\n --CHILD--> [6E2Z] Mental or behavioural disorders associated with pregnancy, childbirth or the puerperium, unspecified", "[KD34] Reactions or intoxications due to drugs administered to fetus or newborn\n Def: A group of paediatric substance-induced conditions associated with health interventions applied to a fetus or newborn using pharmaceutical products....\n --EXCLUDES--> [?] Withdrawal symptoms from therapeutic use of drugs in newborn\n Def: A paediatric condition characterised by the presence of symptoms due to drug withdrawal in a newborn....\n --PARENT--> [?] Certain disorders originating in the perinatal period\n Def: A group of any other paediatric conditions that occur during the period of time around childbirth, especially the five months before and one month after birth....", "[KD34] Reactions or intoxications due to drugs administered to fetus or newborn\n Def: A group of paediatric substance-induced conditions associated with health interventions applied to a fetus or newborn using pharmaceutical products....\n --EXCLUDES--> [?] Neonatal hyperbilirubinaemia due to drugs or toxins transmitted from mother\n --PARENT--> [?] Neonatal hyperbilirubinaemia due to drugs or toxins\n Def: A condition characterised as an increased level of bilirubin above 85 umol/l (5 mg/dL) which manifests as yellowing of the eyes, skin, and other tissues of a newborn due to the transmission of any dru...", "[KB08.2] Congenital hypotonia\n Def: A paediatric condition characterised by abnormally decreased muscle tone that is present at birth in a newborn....\n --PARENT--> [KB08] Disorders of muscle tone of newborn\n Def: A group of paediatric conditions characterised by abnormal muscle tone in a newborn....\n --PARENT--> [?] Neurological disorders specific to the perinatal or neonatal period\n Def: A group of paediatric conditions characterised by an abnormal change in the cerebral status of a newborn....", "[KB08.2] Congenital hypotonia\n Def: A paediatric condition characterised by abnormally decreased muscle tone that is present at birth in a newborn....\n --PARENT--> [KB08] Disorders of muscle tone of newborn\n Def: A group of paediatric conditions characterised by abnormal muscle tone in a newborn....\n --CHILD--> [KB08.2] Congenital hypotonia\n Def: A paediatric condition characterised by abnormally decreased muscle tone that is present at birth in a newborn...." ]
6E20
Mental or behavioural disorders associated with pregnancy, childbirth or the puerperium, without psychotic symptoms
[ { "from_icd11": "6E20", "icd10_code": "F53", "icd10_title": "Mental and behavioral disorders associated with the puerperium, not elsewhere classified" }, { "from_icd11": "KD34", "icd10_code": "P93", "icd10_title": "Reactions and intoxications due to drugs administered to newborn" }, { "from_icd11": "KB08.2", "icd10_code": "P942", "icd10_title": "Congenital hypotonia" }, { "from_icd11": "EC20.02", "icd10_code": "Q828", "icd10_title": "Other specified congenital malformations of skin" }, { "from_icd11": "EC20.02", "icd10_code": "Q804", "icd10_title": "Harlequin fetus" }, { "from_icd11": "EC20.02", "icd10_code": "Q802", "icd10_title": "Lamellar ichthyosis" }, { "from_icd11": "QA48.1", "icd10_code": "Z391", "icd10_title": "Encounter for care and examination of lactating mother" }, { "from_icd11": "KB60.1", "icd10_code": "P701", "icd10_title": "Syndrome of infant of a diabetic mother" }, { "from_icd11": "1C1D.0", "icd10_code": "A660", "icd10_title": "Initial lesions of yaws" }, { "from_icd11": "KD35", "icd10_code": "P961", "icd10_title": "Neonatal withdrawal symptoms from maternal use of drugs of addiction" }, { "from_icd11": "KB60.0", "icd10_code": "P700", "icd10_title": "Syndrome of infant of mother with gestational diabetes" } ]
F53
Mental and behavioral disorders associated with the puerperium, not elsewhere classified
Currently, laparoscopic technique is used for various surgeries; thus, opportunity to perform laparoscopic surgery has increased for many surgeons. The laparoscopic approach has advantages not only for patients but also for surgeons, i.e., less pain, smaller wounds, earlier recovery, and a magnified view. LTPE is a challenging and complicated operation, but some studies have reported on the safety and feasibility of it not only for urologic or gynecologic malignancies but also colorectal malignancies . This is our initial experience with LTPE, and so far, we have not encountered any complications. We have routinely performed lateral lymph node dissection for locally advanced lower rectal cancer, and we believe that this previous experience enabled our current success. Upon histopathological analysis, no apparent invasion of the tumor to adjacent organs was observed, but this was difficult to detect before the surgery; therefore, this patient should have been treated by TPE. This case did not include a posterior invasion, so the surgery time was comparatively short. We did not reconstruct the perineal defect, change the patient’s position, or place ureteral catheters after dissecting the ureters. We believe that these factors contributed to shortening the surgery time. We did not monitor the urine volume after dissecting the ureters, but intraoperative and postoperative complications did not occur.
3.912109
0.407471
sec[1]/sec[0]/p[0]
en
0.999996
27460130
https://doi.org/10.1186/s40792-016-0198-6
[ "this", "laparoscopic", "surgeons", "ltpe", "malignancies", "experience", "complications", "believe", "that", "invasion" ]
[ { "code": "4A01.03", "title": "Transient hypogammaglobulinaemia of infancy" }, { "code": "PK9B.0", "title": "General or plastic surgery devices associated with injury or harm, diagnostic or monitoring devices" }, { "code": "PK9B.1", "title": "General or plastic surgery devices associated with injury or harm, therapeutic, nonsurgical or rehabilitative devices" }, { "code": "2D4Z", "title": "Unspecified malignant neoplasms of unspecified sites" }, { "code": "2E2Z", "title": "Malignant neoplasm metastasis, unspecified" }, { "code": "2B70.Z", "title": "Malignant neoplasms of oesophagus, unspecified" }, { "code": "2B33.Y", "title": "Other malignant haematopoietic neoplasms without further specification" }, { "code": "2B31.1", "title": "Histiocytic sarcoma" }, { "code": "9D5Z", "title": "Subjective visual experiences, unspecified" }, { "code": "9D5Y", "title": "Other specified subjective visual experiences" } ]
=== ICD-11 CODES FOUND === [4A01.03] Transient hypogammaglobulinaemia of infancy Also known as: Transient hypogammaglobulinaemia of infancy | immunoglobulin maturational delay | THI - [transient hypogammaglobulinaemia of infancy] [PK9B.0] General or plastic surgery devices associated with injury or harm, diagnostic or monitoring devices Also known as: General or plastic surgery devices associated with injury or harm, diagnostic or monitoring devices | General or plastic surgery devices associated with injury or harm, diagnostic laparoscopic equipment | General or plastic surgery devices associated with injury or harm, needle biopsy equipment | General or plastic surgery devices associated with injury or harm, skin biopsy equipment Excludes: Circumstances associated with a surgical or other medical device influencing the episode of care without injury or harm [PK9B.1] General or plastic surgery devices associated with injury or harm, therapeutic, nonsurgical or rehabilitative devices Definition: A general- or plastic-surgery device was involved in an adverse incident that occurred in a therapeutic (nonsurgical) and rehabilitative task Also known as: General or plastic surgery devices associated with injury or harm, therapeutic, nonsurgical or rehabilitative devices | General or plastic surgery devices associated with adverse incidents, botox injection equipment | General or plastic surgery devices associated with adverse incidents, therapeutic laparoscopic equipment Excludes: Circumstances associated with a surgical or other medical device influencing the episode of care without injury or harm [2D4Z] Unspecified malignant neoplasms of unspecified sites Also known as: Unspecified malignant neoplasms of unspecified sites | malignancy of unspecified site | malignancy unspecified primary site | malignant growth of unspecified site | malignant mass of unspecified site [2E2Z] Malignant neoplasm metastasis, unspecified Also known as: Malignant neoplasm metastasis, unspecified | secondary malignant neoplasm | metastasis | metastases | disseminated metastases [2B70.Z] Malignant neoplasms of oesophagus, unspecified Also known as: Malignant neoplasms of oesophagus, unspecified | Malignant neoplasms of oesophagus | cancer of oesophagus | oesophageal malignancy | oesophageal cancer [2B33.Y] Other malignant haematopoietic neoplasms without further specification Also known as: Other malignant haematopoietic neoplasms without further specification | Malignant neoplasm blood other | Haematological malignancy NOS | Neoplasm blood benign or unspecified [2B31.1] Histiocytic sarcoma Also known as: Histiocytic sarcoma | Malignant Histiocytosis Includes: Malignant Histiocytosis [9D5Z] Subjective visual experiences, unspecified Also known as: Subjective visual experiences, unspecified [9D5Y] Other specified subjective visual experiences Also known as: Other specified subjective visual experiences | Sudden visual loss | sudden loss of vision | Chromatopsia | Metamorphopsia Includes: Sudden visual loss === GRAPH WALKS === --- Walk 1 --- [4A01.03] Transient hypogammaglobulinaemia of infancy --PARENT--> [4A01.0] Immunodeficiencies with predominantly antibody defects Def: A disorder characterised by an inability to mount a normal immune response due to antibody (i.e. immunoglobulin) defects... --CHILD--> [4A01.02] Specific antibody deficiency with normal immunoglobulin concentrations or normal number of B cells --- Walk 2 --- [4A01.03] Transient hypogammaglobulinaemia of infancy --PARENT--> [4A01.0] Immunodeficiencies with predominantly antibody defects Def: A disorder characterised by an inability to mount a normal immune response due to antibody (i.e. immunoglobulin) defects... --CHILD--> [4A01.00] Hereditary agammaglobulinaemia with profoundly reduced or absent B cells Def: This refers to a hereditary type of primary immune deficiency disease characterised by a reduction in all types of gamma globulins, and rare X-linked genetic disorder that affects the body's ability t... --- Walk 3 --- [PK9B.0] General or plastic surgery devices associated with injury or harm, diagnostic or monitoring devices --PARENT--> [PK9B] General or plastic surgery devices, implants or grafts associated with injury or harm --EXCLUDES--> [?] Circumstances associated with a surgical or other medical device influencing the episode of care without injury or harm --- Walk 4 --- [PK9B.0] General or plastic surgery devices associated with injury or harm, diagnostic or monitoring devices --EXCLUDES--> [?] Circumstances associated with a surgical or other medical device influencing the episode of care without injury or harm --EXCLUDES--> [?] Mode of injury or harm associated with a surgical or other medical device, implant or graft --- Walk 5 --- [PK9B.1] General or plastic surgery devices associated with injury or harm, therapeutic, nonsurgical or rehabilitative devices Def: A general- or plastic-surgery device was involved in an adverse incident that occurred in a therapeutic (nonsurgical) and rehabilitative task... --EXCLUDES--> [?] Circumstances associated with a surgical or other medical device influencing the episode of care without injury or harm --CHILD--> [?] Functional device failure without injury or harm Def: A device not working or operating correctly, or that has stopped functioning after a period of function, but without documented injury or harm to the patient.... --- Walk 6 --- [PK9B.1] General or plastic surgery devices associated with injury or harm, therapeutic, nonsurgical or rehabilitative devices Def: A general- or plastic-surgery device was involved in an adverse incident that occurred in a therapeutic (nonsurgical) and rehabilitative task... --EXCLUDES--> [?] Circumstances associated with a surgical or other medical device influencing the episode of care without injury or harm --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....
[ "[4A01.03] Transient hypogammaglobulinaemia of infancy\n --PARENT--> [4A01.0] Immunodeficiencies with predominantly antibody defects\n Def: A disorder characterised by an inability to mount a normal immune response due to antibody (i.e. immunoglobulin) defects...\n --CHILD--> [4A01.02] Specific antibody deficiency with normal immunoglobulin concentrations or normal number of B cells", "[4A01.03] Transient hypogammaglobulinaemia of infancy\n --PARENT--> [4A01.0] Immunodeficiencies with predominantly antibody defects\n Def: A disorder characterised by an inability to mount a normal immune response due to antibody (i.e. immunoglobulin) defects...\n --CHILD--> [4A01.00] Hereditary agammaglobulinaemia with profoundly reduced or absent B cells\n Def: This refers to a hereditary type of primary immune deficiency disease characterised by a reduction in all types of gamma globulins, and rare X-linked genetic disorder that affects the body's ability t...", "[PK9B.0] General or plastic surgery devices associated with injury or harm, diagnostic or monitoring devices\n --PARENT--> [PK9B] General or plastic surgery devices, implants or grafts associated with injury or harm\n --EXCLUDES--> [?] Circumstances associated with a surgical or other medical device influencing the episode of care without injury or harm", "[PK9B.0] General or plastic surgery devices associated with injury or harm, diagnostic or monitoring devices\n --EXCLUDES--> [?] Circumstances associated with a surgical or other medical device influencing the episode of care without injury or harm\n --EXCLUDES--> [?] Mode of injury or harm associated with a surgical or other medical device, implant or graft", "[PK9B.1] General or plastic surgery devices associated with injury or harm, therapeutic, nonsurgical or rehabilitative devices\n Def: A general- or plastic-surgery device was involved in an adverse incident that occurred in a therapeutic (nonsurgical) and rehabilitative task...\n --EXCLUDES--> [?] Circumstances associated with a surgical or other medical device influencing the episode of care without injury or harm\n --CHILD--> [?] Functional device failure without injury or harm\n Def: A device not working or operating correctly, or that has stopped functioning after a period of function, but without documented injury or harm to the patient....", "[PK9B.1] General or plastic surgery devices associated with injury or harm, therapeutic, nonsurgical or rehabilitative devices\n Def: A general- or plastic-surgery device was involved in an adverse incident that occurred in a therapeutic (nonsurgical) and rehabilitative task...\n --EXCLUDES--> [?] Circumstances associated with a surgical or other medical device influencing the episode of care without injury or harm\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...." ]
4A01.03
Transient hypogammaglobulinaemia of infancy
[ { "from_icd11": "4A01.03", "icd10_code": "D807", "icd10_title": "Transient hypogammaglobulinemia of infancy" }, { "from_icd11": "PK9B.0", "icd10_code": "Y810", "icd10_title": "Diagnostic and monitoring general- and plastic-surgery devices associated with adverse incidents" }, { "from_icd11": "PK9B.1", "icd10_code": "Y811", "icd10_title": "Therapeutic (nonsurgical) and rehabilitative general- and plastic-surgery devices associated with adverse incidents" }, { "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" } ]
D807
Transient hypogammaglobulinemia of infancy
The patient arrived at the National Hospital of Sri Lanka 22 hours after ingestion of the poison, including 4 hours for transport from the local hospital. On admission to the National Hospital of Sri Lanka, he was drowsy and confused, but arousable. He had a shallow respiratory effort and marked central and peripheral cyanosis. On admission the heart rate was 120 beats/min with regular rhythm, blood pressure 100/60 mmHg. The respiratory rate was 20 breaths/min, with a pulse oximetry of 77% on room air and clear lungs on auscultation. The abdomen was soft, with epigastric tenderness. Neurological examination was unremarkable. The arterial blood gas analysis was as follows; pH – 7.24, HCO 3− – 12 mmol/l, pCO 2 – 28 mmHg, pO 2 : 239 mmHg and O 2 saturation – 100%. Intensified monitoring was commenced and supportive care was provided with IV fluids and supplementary O 2 (6 l/min) via face mask. Although the patient showed mild improvement in his respiratory status, there was no change in his cyanosis yet and pulse oximetry demonstrated an oxygen saturation fluctuating between 75%-85%. Serum methaemoglobin levels were not measured due to the non-availability of facilities. The patient’s clinical condition continued to deteriorate with worsening drowsiness, increased respiratory rate (30 breaths/min) and tachycardia (130 beats/min), so it was decided it to commence on exchange transfusion without delay.
3.566406
0.983398
sec[1]/p[1]
en
0.999997
25292188
https://doi.org/10.1186/1756-0500-7-700
[ "respiratory", "mmhg", "national", "lanka", "hours", "cyanosis", "beats", "blood", "breaths", "pulse" ]
[ { "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": "RA20", "title": "National emergency code 01" }, { "code": "RA24", "title": "National emergency code 05" }, { "code": "RA21", "title": "National emergency code 02" }, { "code": "RA25", "title": "National emergency code 06" }, { "code": "RA26", "title": "National emergency code 07" } ]
=== 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 [RA20] National emergency code 01 Also known as: National emergency code 01 [RA24] National emergency code 05 Also known as: National emergency code 05 [RA21] National emergency code 02 Also known as: National emergency code 02 [RA25] National emergency code 06 Also known as: National emergency code 06 [RA26] National emergency code 07 Also known as: National emergency code 07 === GRAPH WALKS === --- Walk 1 --- [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 2 --- [CB7Z] Diseases of the respiratory system, unspecified --PARENT--> [12] Diseases of the respiratory system --RELATED_TO--> [?] Symptoms, signs or clinical findings of the respiratory system --- 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--> [CB41.2] 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 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--> [?] Acute respiratory distress syndrome Def: Acute respiratory distress syndrome ("ARDS") is a life-threatening inflammation with oedema in the lungs which leads to severe respiratory failure. ARDS is a clinical syndrome of lung injury with hypo... --CHILD--> [?] Adult acute respiratory distress syndrome Def: Progressive, life-threatening respiratory insufficiency in the absence of known lung diseases, frequently following a systemic insult such as severe pneumonia, aspiration pneumonitis, sepsis, surgery ... --- 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--> [CB41.20] 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... --- 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--> [CB41.21] 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...
[ "[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", "[CB7Z] Diseases of the respiratory system, unspecified\n --PARENT--> [12] Diseases of the respiratory system\n --RELATED_TO--> [?] Symptoms, signs or clinical findings of the respiratory system", "[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--> [CB41.2] 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] 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--> [?] Acute respiratory distress syndrome\n Def: Acute respiratory distress syndrome (\"ARDS\") is a life-threatening inflammation with oedema in the lungs which leads to severe respiratory failure. ARDS is a clinical syndrome of lung injury with hypo...\n --CHILD--> [?] Adult acute respiratory distress syndrome\n Def: Progressive, life-threatening respiratory insufficiency in the absence of known lung diseases, frequently following a systemic insult such as severe pneumonia, aspiration pneumonitis, sepsis, surgery ...", "[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...", "[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..." ]
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": "RA20", "icd10_code": "XXII", "icd10_title": "" } ]
J989
Respiratory disorder, unspecified
Despite the recent introduction of endoscopic interventions, bypass surgery remains a treatment of choice for palliating symptoms in patients with advanced pancreatic cancer. Bypass surgery for cancer of the pancreatic head is usually done to relieve the obstructive symptoms in the biliary and/or digestive system. However, it is uncommon for such patients to require pancreatic duct drainage for recurrent obstructive pancreatitis. In this article, we report a surgical technique of triple bypass consisting of Roux-en-Y hepaticojejunostomy, gastrojejunostomy, and pancreaticojejunostomy. Although triple bypass is a complex procedure, this technique can simultaneously resolve the three problems in patients with advanced pancreatic cancer, including obstructive jaundice, duodenal stenosis, and recurrent obstructive pancreatitis. In more specific, we selected triple bypass for this particular case because of the following reasons: (i) Although biliary obstruction in the present case was initially treated by endoscopic stent placement, repeated endoscopic approach to the papilla for stent exchange was subsequently impossible due to exacerbated duodenal stenosis; (ii) The patient complained of nausea and appetite loss possibly due to duodenal stenosis; (iii) The patient suffered from recurrent obstructive pancreatitis associated with pancreatic pseudocyst untreatable by medication or endoscopic procedures.
4.09375
0.692383
sec[1]/sec[2]/p[0]
en
0.999997
27495991
https://doi.org/10.1186/s40792-016-0210-1
[ "bypass", "pancreatic", "obstructive", "endoscopic", "patients", "cancer", "recurrent", "pancreatitis", "this", "triple" ]
[ { "code": "QB6Y", "title": "Other specified surgical or postsurgical states" }, { "code": "PL12.3", "title": "Obstruction of device, as mode of injury or harm" }, { "code": "BC62", "title": "Accessory pathway" }, { "code": "QB50.1", "title": "Presence of aortocoronary bypass graft" }, { "code": "FA11.0", "title": "Arthropathy following intestinal bypass" }, { "code": "DC3Z", "title": "Diseases of pancreas, unspecified" }, { "code": "DC3Y", "title": "Other specified diseases of pancreas" }, { "code": "LB21.3", "title": "Agenesis-aplasia of pancreas" }, { "code": "LB21.Z", "title": "Structural developmental anomalies of pancreas, unspecified" }, { "code": "DC35.0", "title": "Atrophy of pancreas" } ]
=== ICD-11 CODES FOUND === [QB6Y] Other specified surgical or postsurgical states Also known as: Other specified surgical or postsurgical states | Presence of intestinal bypass or anastomosis | intestinal bypass and anastomosis status | anastomosis status | intestinal bypass status [PL12.3] Obstruction of device, as mode of injury or harm Definition: Obstruction associated with prosthetic devices, grafts or implants Also known as: Obstruction of device, as mode of injury or harm | occlusion shunt | blockage of device causing obstruction as mode of injury | blocked tube causing obstruction as mode of injury | occlusion of device causing obstruction as mode of injury Excludes: Obstruction of device without injury or harm [BC62] Accessory pathway Definition: An additional electrical connection which typically bypasses the AV node, typically inserting directly into atrial and ventricular myocardium, but may also connect to the specialised conduction system (e.g., the bundle of His, right or left bundles, or one of the fascicles). Also known as: Accessory pathway | anomalous AV pathway | anomalous AV connection | anomalous AV bypass pathway | anomalous AV bypass tract [QB50.1] Presence of aortocoronary bypass graft Also known as: Presence of aortocoronary bypass graft | aortocoronary bypass status | replacement of coronary artery by artificial or mechanical device or prosthesis [FA11.0] Arthropathy following intestinal bypass Also known as: Arthropathy following intestinal bypass | Jejunoileal arthropathy | Arthropathy following intestinal bypass, multiple sites | Arthropathy following intestinal bypass, shoulder region | Arthropathy following intestinal bypass, acromioclavicular joint [DC3Z] Diseases of pancreas, unspecified Also known as: Diseases of pancreas, unspecified [DC3Y] Other specified diseases of pancreas Also known as: Other specified diseases of pancreas | Calculus of pancreas | pancreas calculi | pancreas duct calculus | pancreas duct lithiasis [LB21.3] Agenesis-aplasia of pancreas Definition: This refers to the failure of an organ to develop during embryonic growth and development due to the absence of primordial tissue of the pancreas. Also known as: Agenesis-aplasia of pancreas | Congenital absence of pancreas | Congenital pancreas absence | Congenital pancreatic absence | Absent pancreas [LB21.Z] Structural developmental anomalies of pancreas, unspecified Also known as: Structural developmental anomalies of pancreas, unspecified | Structural developmental anomalies of pancreas | malformations of pancreas | anomalies of pancreas | congenital abnormality of pancreas [DC35.0] Atrophy of pancreas Also known as: Atrophy of pancreas | pancreatic atrophy | pancreas ductal atrophy === GRAPH WALKS === --- Walk 1 --- [QB6Y] Other specified surgical or postsurgical states --PARENT--> [?] Surgical or postsurgical states --RELATED_TO--> [?] Presence of cataract surgery --- Walk 2 --- [QB6Y] Other specified surgical or postsurgical states --PARENT--> [?] Surgical or postsurgical states --CHILD--> [QB62] Attention to artificial openings --- Walk 3 --- [PL12.3] Obstruction of device, as mode of injury or harm Def: Obstruction associated with prosthetic devices, grafts or implants... --PARENT--> [PL12] Mode of injury or harm associated with a surgical or other medical device, implant or graft --CHILD--> [PL12.0] Structural device failure, as mode of injury or harm Def: Harm arising due to mechanical or material device failure not related to the installation of the device.... --- Walk 4 --- [PL12.3] Obstruction of device, as mode of injury or harm Def: Obstruction associated with prosthetic devices, grafts or implants... --EXCLUDES--> [?] Obstruction of device without injury or harm Def: A device that has become obstructed or blocked but without any documented injury or harm.... --EXCLUDES--> [?] Obstruction of device, as mode of injury or harm Def: Obstruction associated with prosthetic devices, grafts or implants... --- Walk 5 --- [BC62] Accessory pathway Def: An additional electrical connection which typically bypasses the AV node, typically inserting directly into atrial and ventricular myocardium, but may also connect to the specialised conduction system... --PARENT--> [?] Cardiac arrhythmia Def: This is any of a large and heterogeneous group of conditions in which there is abnormal electrical activity in the heart. The heartbeat may be too fast or too slow, and may be regular or irregular.... --RELATED_TO--> [?] Dysfunction or complication of pacemaker, pacemaker lead or implantable cardioverter defibrillator, not elsewhere classified --- Walk 6 --- [BC62] Accessory pathway Def: An additional electrical connection which typically bypasses the AV node, typically inserting directly into atrial and ventricular myocardium, but may also connect to the specialised conduction system... --PARENT--> [?] Cardiac arrhythmia Def: This is any of a large and heterogeneous group of conditions in which there is abnormal electrical activity in the heart. The heartbeat may be too fast or too slow, and may be regular or irregular.... --CHILD--> [BC60] Atrial premature depolarization Def: Cardiac electrical depolarization arising from the atria, occurring earlier than the expected sinus beat...
[ "[QB6Y] Other specified surgical or postsurgical states\n --PARENT--> [?] Surgical or postsurgical states\n --RELATED_TO--> [?] Presence of cataract surgery", "[QB6Y] Other specified surgical or postsurgical states\n --PARENT--> [?] Surgical or postsurgical states\n --CHILD--> [QB62] Attention to artificial openings", "[PL12.3] Obstruction of device, as mode of injury or harm\n Def: Obstruction associated with prosthetic devices, grafts or implants...\n --PARENT--> [PL12] Mode of injury or harm associated with a surgical or other medical device, implant or graft\n --CHILD--> [PL12.0] Structural device failure, as mode of injury or harm\n Def: Harm arising due to mechanical or material device failure not related to the installation of the device....", "[PL12.3] Obstruction of device, as mode of injury or harm\n Def: Obstruction associated with prosthetic devices, grafts or implants...\n --EXCLUDES--> [?] Obstruction of device without injury or harm\n Def: A device that has become obstructed or blocked but without any documented injury or harm....\n --EXCLUDES--> [?] Obstruction of device, as mode of injury or harm\n Def: Obstruction associated with prosthetic devices, grafts or implants...", "[BC62] Accessory pathway\n Def: An additional electrical connection which typically bypasses the AV node, typically inserting directly into atrial and ventricular myocardium, but may also connect to the specialised conduction system...\n --PARENT--> [?] Cardiac arrhythmia\n Def: This is any of a large and heterogeneous group of conditions in which there is abnormal electrical activity in the heart. The heartbeat may be too fast or too slow, and may be regular or irregular....\n --RELATED_TO--> [?] Dysfunction or complication of pacemaker, pacemaker lead or implantable cardioverter defibrillator, not elsewhere classified", "[BC62] Accessory pathway\n Def: An additional electrical connection which typically bypasses the AV node, typically inserting directly into atrial and ventricular myocardium, but may also connect to the specialised conduction system...\n --PARENT--> [?] Cardiac arrhythmia\n Def: This is any of a large and heterogeneous group of conditions in which there is abnormal electrical activity in the heart. The heartbeat may be too fast or too slow, and may be regular or irregular....\n --CHILD--> [BC60] Atrial premature depolarization\n Def: Cardiac electrical depolarization arising from the atria, occurring earlier than the expected sinus beat..." ]
QB6Y
Other specified surgical or postsurgical states
[ { "from_icd11": "QB6Y", "icd10_code": "Z98890", "icd10_title": "Other specified postprocedural states" }, { "from_icd11": "BC62", "icd10_code": "I498", "icd10_title": "Other specified cardiac arrhythmias" }, { "from_icd11": "BC62", "icd10_code": "I49", "icd10_title": "Other cardiac arrhythmias" }, { "from_icd11": "QB50.1", "icd10_code": "Z951", "icd10_title": "Presence of aortocoronary bypass graft" }, { "from_icd11": "FA11.0", "icd10_code": "M0200", "icd10_title": "Arthropathy following intestinal bypass, unspecified site" }, { "from_icd11": "FA11.0", "icd10_code": "M020", "icd10_title": "Arthropathy following intestinal bypass" }, { "from_icd11": "DC3Z", "icd10_code": "K8681", "icd10_title": "Exocrine pancreatic insufficiency" }, { "from_icd11": "DC3Z", "icd10_code": "K8689", "icd10_title": "Other specified diseases of pancreas" }, { "from_icd11": "DC3Z", "icd10_code": "K869", "icd10_title": "Disease of pancreas, unspecified" }, { "from_icd11": "DC3Z", "icd10_code": "K868", "icd10_title": "Other specified diseases of pancreas" }, { "from_icd11": "DC3Z", "icd10_code": "K87", "icd10_title": "Disorders of gallbladder, biliary tract and pancreas in diseases classified elsewhere" }, { "from_icd11": "DC3Z", "icd10_code": "K80-K87", "icd10_title": "" }, { "from_icd11": "DC3Z", "icd10_code": "K86", "icd10_title": "Other diseases of pancreas" }, { "from_icd11": "DC3Z", "icd10_code": "K871", "icd10_title": "" }, { "from_icd11": "LB21.Z", "icd10_code": "Q450", "icd10_title": "Agenesis, aplasia and hypoplasia of pancreas" } ]
Z98890
Other specified postprocedural states
A previously healthy 25-year-old Middle Eastern male self-presented to our general hospital three years ago with sternal chest pain of a gradual onset, without any associated symptoms. He had no family history of inheritable conditions and no history of drugs or allergies. The patient was a non-smoker without any alcohol intake. On physical examination his vital signs were within the normal range and sternal tenderness was elicited on palpation. No other sites of pain were reported, and review of systems was unremarkable. A posterior-anterior (PA) chest radiograph showed no abnormalities. A computed tomography (CT) scan of the chest was performed, which showed a lytic bone lesion in the sternum . Biopsy of the lesion was inconclusive. Opting to receive only oral analgesics (Paracetamol, Ibuprofen) as needed for the pain following a discussion of the existing management options, the lesion resolved spontaneously within a year with no deviations from the initial management plan. The patient presented twice in clinic for follow-up since his initial presentation. He described a gradually decreasing need for analgesia which was ceased after 3 months, with no impact on his quality of life. Routine labs remained within normal range and no complications were observed. He was subsequently lost to follow-up. Fig. 1 (A) Axial and (B) Saggital CT chest with a lytic lesion of the sternum in bone window. Fig. 1
3.6875
0.987305
sec[1]/p[0]
en
0.999999
PMC8885459
https://doi.org/10.1016/j.amsu.2022.103401
[ "chest", "lesion", "pain", "within", "sternal", "without", "range", "which", "lytic", "bone" ]
[ { "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": "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" } ]
=== 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 [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 === 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--> [?] Injury, poisoning or certain other consequences of external causes Def: !markdown In the ICD, injury means physical or physiological bodily harm resulting from interaction of the body with energy (mechanical, thermal, electrical, chemical or radiant, or due to extreme pre... --- Walk 3 --- [CB27] Pleural effusion Def: Presence of fluid in the pleural cavity resulting from excessive transudation or exudation from the pleural surfaces.... --EXCLUDES--> [?] Pleurisy Def: Pleurisy or Pleuritis is the medical term for inflammation of the pleura. The most common cause of pleuritis is infection, but it can also be caused by lupus, rheumatoid arthritis, and certain medicin... --CHILD--> [?] Chronic pleurisy --- Walk 4 --- [CB27] Pleural effusion Def: Presence of fluid in the pleural cavity resulting from excessive transudation or exudation from the pleural surfaces.... --EXCLUDES--> [?] Tuberculosis of the respiratory system Def: This is a progressive or chronic disease resulting from infection with the bacterium Mycobacterium tuberculosis or other bacteria in the M. tuberculosis complex: M. bovis, M. africanum, M. canetti, M.... --CHILD--> [?] Tuberculosis of lung, without mention of bacteriological or histological confirmation Def: This is a common, and in many cases lethal, infectious disease of the lung caused by various strains of mycobacteria, usually Mycobacterium tuberculosis. This diagnosis is without mention of bacteriol... --- Walk 5 --- [CA44] Pyothorax Def: Suppurative inflammation of the pleural space, typically due to acute bacterial infection. It can occur as a complication of pneumonia, thoracotomy, abscesses (lung, hepatic, or subdiaphragmatic), or ... --EXCLUDES--> [?] Tuberculous pleurisy, without mention of bacteriological or histological confirmation Def: This is a common, and in many cases lethal, infectious disease caused by various strains of mycobacteria, usually Mycobacterium tuberculosis, with an inflammation of the pleura. This diagnosis is with... --PARENT--> [?] Tuberculosis of the respiratory system Def: This is a progressive or chronic disease resulting from infection with the bacterium Mycobacterium tuberculosis or other bacteria in the M. tuberculosis complex: M. bovis, M. africanum, M. canetti, M.... --- Walk 6 --- [CA44] Pyothorax Def: Suppurative inflammation of the pleural space, typically due to acute bacterial infection. It can occur as a complication of pneumonia, thoracotomy, abscesses (lung, hepatic, or subdiaphragmatic), or ... --EXCLUDES--> [?] Tuberculous pleurisy, without mention of bacteriological or histological confirmation Def: This is a common, and in many cases lethal, infectious disease caused by various strains of mycobacteria, usually Mycobacterium tuberculosis, with an inflammation of the pleura. This diagnosis is with... --CHILD--> [?] Bronchopleural tuberculosis
[ "[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--> [?] 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...", "[CB27] Pleural effusion\n Def: Presence of fluid in the pleural cavity resulting from excessive transudation or exudation from the pleural surfaces....\n --EXCLUDES--> [?] Pleurisy\n Def: Pleurisy or Pleuritis is the medical term for inflammation of the pleura. The most common cause of pleuritis is infection, but it can also be caused by lupus, rheumatoid arthritis, and certain medicin...\n --CHILD--> [?] Chronic pleurisy", "[CB27] Pleural effusion\n Def: Presence of fluid in the pleural cavity resulting from excessive transudation or exudation from the pleural surfaces....\n --EXCLUDES--> [?] Tuberculosis of the respiratory system\n Def: This is a progressive or chronic disease resulting from infection with the bacterium Mycobacterium tuberculosis or other bacteria in the M. tuberculosis complex: M. bovis, M. africanum, M. canetti, M....\n --CHILD--> [?] Tuberculosis of lung, without mention of bacteriological or histological confirmation\n Def: This is a common, and in many cases lethal, infectious disease of the lung caused by various strains of mycobacteria, usually Mycobacterium tuberculosis. This diagnosis is without mention of bacteriol...", "[CA44] Pyothorax\n Def: Suppurative inflammation of the pleural space, typically due to acute bacterial infection. It can occur as a complication of pneumonia, thoracotomy, abscesses (lung, hepatic, or subdiaphragmatic), or ...\n --EXCLUDES--> [?] Tuberculous pleurisy, without mention of bacteriological or histological confirmation\n Def: This is a common, and in many cases lethal, infectious disease caused by various strains of mycobacteria, usually Mycobacterium tuberculosis, with an inflammation of the pleura. This diagnosis is with...\n --PARENT--> [?] Tuberculosis of the respiratory system\n Def: This is a progressive or chronic disease resulting from infection with the bacterium Mycobacterium tuberculosis or other bacteria in the M. tuberculosis complex: M. bovis, M. africanum, M. canetti, M....", "[CA44] Pyothorax\n Def: Suppurative inflammation of the pleural space, typically due to acute bacterial infection. It can occur as a complication of pneumonia, thoracotomy, abscesses (lung, hepatic, or subdiaphragmatic), or ...\n --EXCLUDES--> [?] Tuberculous pleurisy, without mention of bacteriological or histological confirmation\n Def: This is a common, and in many cases lethal, infectious disease caused by various strains of mycobacteria, usually Mycobacterium tuberculosis, with an inflammation of the pleura. This diagnosis is with...\n --CHILD--> [?] Bronchopleural tuberculosis" ]
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 case we describe presented unusual clinical features. Most conspicuous were the widespread, very painful bone lesions with soft tissue involvement which were interpreted as multiple myeloid sarcomas and extensive bone infarcts, not mere marrow infiltration. The validity of this diagnosis is supported by the gradual, protracted resolution of these lesions taking place during and after therapy. To the best of our knowledge, only four cases, including the present one, have been reported of very young AML patients displaying myelomonocytic features, myeloid sarcomas, and involvement of the MLL - ELL fusion gene . The four patients have similar cytogenetic and genetic ( MLL - ELL fusion) features. Three of them had a three-way translocation generating the MLL - ELL fusion: the present case with t(8;19;11)(q24;p13;q23), a female newborn with t(1;19;11)(p36;p13.11;q23) , and a three-month-old boy with t(6;19;11)(p22;p13;q23) . None of the patients had the type 1 MLL - ELL fusion (see above). In the patient with t(1;19;11)(p36;p13.11;q23), the data suggest an MLL exon 9- ELL exon 6 fusion transcript, similar to our case . In a two-month-old child reported by De Braekeler et al, the genomic breakpoints in MLL and ELL indicated an MLL exon 9- ELL exon 3 fusion transcript . In the three-month-old boy with t(6;19;11)(p22;p13;q23), the translocation resulted in an MLL exon 8- ELL exon 3 fusion transcript .
4.246094
0.594238
sec[2]/p[3]
en
0.999997
26949571
https://doi.org/10.1186/s40164-016-0037-2
[ "fusion", "exon", "three", "features", "patients", "transcript", "bone", "lesions", "involvement", "myeloid" ]
[ { "code": "FA34.4", "title": "Ankylosis of joint" }, { "code": "LB17.2", "title": "Persistent cloaca" }, { "code": "FB00", "title": "Ankylosis of spinal joint" }, { "code": "LD2G", "title": "Conjoined twins" }, { "code": "LB79.0", "title": "Fused fingers" }, { "code": "1D45", "title": "Sandfly fever" }, { "code": "PA09", "title": "Unintentional land transport traffic event injuring an occupant of a low powered passenger vehicle" }, { "code": "LD50.Y", "title": "Other specified number anomalies of chromosome X" }, { "code": "PA19", "title": "Unintentional land transport nontraffic event injuring an occupant of a low powered passenger vehicle" }, { "code": "NA82.4", "title": "Multiple fractures of ribs" } ]
=== ICD-11 CODES FOUND === [FA34.4] Ankylosis of joint Definition: The term ankylosis denotes restricted movement in the joint, and it can be bony or fibrous. Most cases are caused by trauma, infection, radiotherapy, or severe arthritic condition. Also known as: Ankylosis of joint | ankylosis | ankylosis of joint, site unspecified | frozen joint | fusion of joint Excludes: stiffness of joint without ankylosis | Ankylosis of spinal joint [LB17.2] Persistent cloaca Definition: A congenital anomaly in which the intestinal, urinary, and reproductive ducts open into a common cavity, a result of the failure of the urorectal septum to form during prenatal development. They occur exclusively in girls and comprise the most complex defect in the spectrum of anorectal malformations. Also known as: Persistent cloaca | anal and urogenital canal fusion | anal fusion | Cloaca NOS [FB00] Ankylosis of spinal joint Also known as: Ankylosis of spinal joint | ankylosis of spine nos | fusion of vertebra NOS | fusion of spine NOS | Ankylosis of cervical spinal joint [LD2G] Conjoined twins Definition: A condition characterised as twins that are physically united at some part or parts of their bodies at the time of birth. Also known as: Conjoined twins | siamese twin | twin fusion | Thoracopagus | thorax-joined twins [LB79.0] Fused fingers Also known as: Fused fingers | complex syndactyly of fingers with synostosis | complex syndactyly of fingers | congenital adhesion of fingers | syndactyly of fingers with fusion of bone Includes: complex syndactyly of fingers with synostosis [1D45] Sandfly fever Also known as: Sandfly fever | sandfly-borne phleboviral disease | pappataci fever | phlebotomus fever | three day fever Includes: pappataci fever | phlebotomus fever [PA09] Unintentional land transport traffic event injuring an occupant of a low powered passenger vehicle Also known as: Unintentional land transport traffic event injuring an occupant of a low powered passenger vehicle | Occupant of three-wheeled motor vehicle injured in transport accident | Occupant of three-wheeled motor vehicle injured in collision with pedestrian or animal | Occupant of three-wheeled motor vehicle injured in collision with pedestrian or animal : person injured while boarding or alighting | Occupant of three-wheeled motor vehicle injured in collision with pedestrian or animal : driver injured in traffic accident [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 [PA19] Unintentional land transport nontraffic event injuring an occupant of a low powered passenger vehicle Also known as: Unintentional land transport nontraffic event injuring an occupant of a low powered passenger vehicle | Occupant of three-wheeled motor vehicle injured in nontraffic accident NOS | Collision NOS involving three-wheeled motor vehicle, nontraffic | Accident NOS involving three-wheeled motor vehicle, nontraffic | Occupant of three-wheeled motor vehicle injured in collision with pedestrian or animal : driver injured in nontraffic accident [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 --- [FA34.4] Ankylosis of joint Def: The term ankylosis denotes restricted movement in the joint, and it can be bony or fibrous. Most cases are caused by trauma, infection, radiotherapy, or severe arthritic condition.... --EXCLUDES--> [?] Ankylosis of spinal joint --CHILD--> [?] Ankylosis of cervical spinal joint --- Walk 2 --- [FA34.4] Ankylosis of joint Def: The term ankylosis denotes restricted movement in the joint, and it can be bony or fibrous. Most cases are caused by trauma, infection, radiotherapy, or severe arthritic condition.... --EXCLUDES--> [?] Stiffness of joint Def: Lack of range of motion of a joint secondary to pain, disease process or congenital malformation not detailed in or used in conjunction with other codes.... --CHILD--> [?] Stiffness of joint, multiple sites --- Walk 3 --- [LB17.2] Persistent cloaca Def: A congenital anomaly in which the intestinal, urinary, and reproductive ducts open into a common cavity, a result of the failure of the urorectal septum to form during prenatal development. They occur... --PARENT--> [LB17] Structural developmental anomalies of anal canal --CHILD--> [LB17.2] Persistent cloaca Def: A congenital anomaly in which the intestinal, urinary, and reproductive ducts open into a common cavity, a result of the failure of the urorectal septum to form during prenatal development. They occur... --- Walk 4 --- [LB17.2] Persistent cloaca Def: A congenital anomaly in which the intestinal, urinary, and reproductive ducts open into a common cavity, a result of the failure of the urorectal septum to form during prenatal development. They occur... --PARENT--> [LB17] Structural developmental anomalies of anal canal --CHILD--> [LB17.0] Anorectal malformations Def: Anorectal malformations (ARMs) are birth defects (due to alterations in embryo development of hindgut or proctodeum) where the anus and rectum (the lower end of the digestive tract) do not develop pro... --- Walk 5 --- [FB00] Ankylosis of spinal joint --PARENT--> [?] Spondylopathies --RELATED_TO--> [?] Collapsed vertebra, not elsewhere classified --- Walk 6 --- [FB00] Ankylosis of spinal joint --PARENT--> [?] Spondylopathies --RELATED_TO--> [?] Nonunion after spinal arthrodesis
[ "[FA34.4] Ankylosis of joint\n Def: The term ankylosis denotes restricted movement in the joint, and it can be bony or fibrous. Most cases are caused by trauma, infection, radiotherapy, or severe arthritic condition....\n --EXCLUDES--> [?] Ankylosis of spinal joint\n --CHILD--> [?] Ankylosis of cervical spinal joint", "[FA34.4] Ankylosis of joint\n Def: The term ankylosis denotes restricted movement in the joint, and it can be bony or fibrous. Most cases are caused by trauma, infection, radiotherapy, or severe arthritic condition....\n --EXCLUDES--> [?] Stiffness of joint\n Def: Lack of range of motion of a joint secondary to pain, disease process or congenital malformation not detailed in or used in conjunction with other codes....\n --CHILD--> [?] Stiffness of joint, multiple sites", "[LB17.2] Persistent cloaca\n Def: A congenital anomaly in which the intestinal, urinary, and reproductive ducts open into a common cavity, a result of the failure of the urorectal septum to form during prenatal development. They occur...\n --PARENT--> [LB17] Structural developmental anomalies of anal canal\n --CHILD--> [LB17.2] Persistent cloaca\n Def: A congenital anomaly in which the intestinal, urinary, and reproductive ducts open into a common cavity, a result of the failure of the urorectal septum to form during prenatal development. They occur...", "[LB17.2] Persistent cloaca\n Def: A congenital anomaly in which the intestinal, urinary, and reproductive ducts open into a common cavity, a result of the failure of the urorectal septum to form during prenatal development. They occur...\n --PARENT--> [LB17] Structural developmental anomalies of anal canal\n --CHILD--> [LB17.0] Anorectal malformations\n Def: Anorectal malformations (ARMs) are birth defects (due to alterations in embryo development of hindgut or proctodeum) where the anus and rectum (the lower end of the digestive tract) do not develop pro...", "[FB00] Ankylosis of spinal joint\n --PARENT--> [?] Spondylopathies\n --RELATED_TO--> [?] Collapsed vertebra, not elsewhere classified", "[FB00] Ankylosis of spinal joint\n --PARENT--> [?] Spondylopathies\n --RELATED_TO--> [?] Nonunion after spinal arthrodesis" ]
FA34.4
Ankylosis of joint
[ { "from_icd11": "FA34.4", "icd10_code": "M24662", "icd10_title": "Ankylosis, left knee" }, { "from_icd11": "FA34.4", "icd10_code": "M24652", "icd10_title": "Ankylosis, left hip" }, { "from_icd11": "FA34.4", "icd10_code": "M24651", "icd10_title": "Ankylosis, right hip" }, { "from_icd11": "FA34.4", "icd10_code": "M24661", "icd10_title": "Ankylosis, right knee" }, { "from_icd11": "FA34.4", "icd10_code": "M24621", "icd10_title": "Ankylosis, right elbow" }, { "from_icd11": "FA34.4", "icd10_code": "M24674", "icd10_title": "Ankylosis, right foot" }, { "from_icd11": "FA34.4", "icd10_code": "M24669", "icd10_title": "Ankylosis, unspecified knee" }, { "from_icd11": "FA34.4", "icd10_code": "M24659", "icd10_title": "Ankylosis, unspecified hip" }, { "from_icd11": "FA34.4", "icd10_code": "M2460", "icd10_title": "Ankylosis, unspecified joint" }, { "from_icd11": "FA34.4", "icd10_code": "M24619", "icd10_title": "Ankylosis, unspecified shoulder" }, { "from_icd11": "FA34.4", "icd10_code": "M24673", "icd10_title": "Ankylosis, unspecified ankle" }, { "from_icd11": "FA34.4", "icd10_code": "M24676", "icd10_title": "Ankylosis, unspecified foot" }, { "from_icd11": "FA34.4", "icd10_code": "M24629", "icd10_title": "Ankylosis, unspecified elbow" }, { "from_icd11": "FA34.4", "icd10_code": "M246", "icd10_title": "Ankylosis of joint" }, { "from_icd11": "LB17.2", "icd10_code": "Q437", "icd10_title": "Persistent cloaca" } ]
M24662
Ankylosis, left knee
A 91-year-old Thai woman with bilateral pseudophakia presented with acute left eye pain and redness. The best-corrected visual acuity was 6/9. On slit-lamp examination of the left eye, diffuse conjunctiva injection and the dendritic ulcer with terminal bulbs, highlighted by fluorescein staining, were observed on the superotemporal side of the cornea . There were no cells in the anterior chamber. She was diagnosed with herpes simplex keratitis (HSK) on the left eye. Noticeably, there was also a localized encapsulated bleb on the superonasal conjunctiva with a negative Seidel test . No peripheral iridectomy was seen and the IOP was 12 mmHg. Fundus examination revealed a cup-to-disc ratio of 0.5 with an intact neural rim. Fig. 1 Composite slit-lamp images of the left eye. a A localized encapsulated bleb with scar tissue in a ring of steel configuration on the superonasal conjunctiva at ten times magnification. Adjacent to the inferior part of the bleb, just above the site of the previous pterygium, is a nodular corneal degeneration and corneal scar. The diffuse conjunctival injection is also observed. b Deep anterior chamber and a sign of epitheliopathy (arrowheads) observed at 16 times magnification. c An examination with fluorescein staining was observed using blue light. The stain highlights the area of the dendritic ulcer and terminal bulbs (arrowheads). The Seidel test was negative over the bleb
3.935547
0.981445
sec[1]/p[0]
en
0.999996
PMC9938554
https://doi.org/10.1186/s13256-023-03784-6
[ "bleb", "conjunctiva", "slit", "lamp", "injection", "dendritic", "ulcer", "terminal", "bulbs", "fluorescein" ]
[ { "code": "CA21.Y", "title": "Other specified emphysema" }, { "code": "CA21.Z", "title": "Emphysema, unspecified" }, { "code": "9C21.Y", "title": "Other specified endophthalmitis" }, { "code": "9D23", "title": "Conjunctival blebitis after glaucoma surgery" }, { "code": "LC51", "title": "Developmental venous malformations involving the skin" }, { "code": "9A6Z", "title": "Disorders of conjunctiva, unspecified" }, { "code": "9A60.Z", "title": "Conjunctivitis, unspecified" }, { "code": "9A60.30", "title": "Ulceration of conjunctiva" }, { "code": "9A6Y", "title": "Other specified disorders of conjunctiva" }, { "code": "NA06.4&XA8PS3", "title": "Haematoma of conjunctiva" } ]
=== ICD-11 CODES FOUND === [CA21.Y] Other specified emphysema Also known as: Other specified emphysema | Airway obstruction with emphysema | chronic obstructive pulmonary emphysema | obstructive emphysema | obstructive lung or pulmonary emphysema [CA21.Z] Emphysema, unspecified Also known as: Emphysema, unspecified | Emphysema | emphysema of lung | pulmonary emphysema | pulmonary emphysema NOS [9C21.Y] Other specified endophthalmitis Also known as: Other specified endophthalmitis | Other endophthalmitis | Parasitic endophthalmitis | Bleb associated endophthalmitis | Iridochoroiditis [9D23] Conjunctival blebitis after glaucoma surgery Also known as: Conjunctival blebitis after glaucoma surgery | postprocedural blebitis | inflammation or infection of postprocedural bleb | Inflammation or infection of postprocedural bleb, stage 1 | Inflammation or infection of postprocedural bleb, stage 2 [LC51] Developmental venous malformations involving the skin Definition: Certain genetically-determined syndromes presenting with venous anomalies in the skin Also known as: Developmental venous malformations involving the skin | Blue rubber bleb naevus syndrome | Bean syndrome (MIM 112200) | Mucocutaneous venous malformations | Glomuvenous malformation [9A6Z] Disorders of conjunctiva, unspecified Also known as: Disorders of conjunctiva, unspecified | conjunctival disease NOS | disease of conjunctiva NOS | conjunctiva lesion NOS [9A60.Z] Conjunctivitis, unspecified Also known as: Conjunctivitis, unspecified | Conjunctivitis | inflammation of conjunctiva | ophthalmia | acute conjunctivitis [9A60.30] Ulceration of conjunctiva Also known as: Ulceration of conjunctiva | conjunctival ulcer [9A6Y] Other specified disorders of conjunctiva Also known as: Other specified disorders of conjunctiva | Secondary disorders of conjunctiva | Disorders of conjunctiva in diseases classified elsewhere | Secondary conjunctivitis | Conjunctivitis in other diseases classified elsewhere === GRAPH WALKS === --- Walk 1 --- [CA21.Y] Other specified emphysema --PARENT--> [CA21] Emphysema Def: Emphysema is defined by abnormal and permanent enlargement of the airspaces that are distal to the terminal bronchioles. This is accompanied by destruction of the airspace walls, without obvious fibro... --CHILD--> [CA21.1] Panlobular emphysema Def: Panlobular (panacinar) emphysema destroys the entire alveolus uniformly and is predominant in the lower half of the lungs. Panlobular emphysema generally is observed in patients with homozygous alpha1... --- Walk 2 --- [CA21.Y] Other specified emphysema --PARENT--> [CA21] Emphysema Def: Emphysema is defined by abnormal and permanent enlargement of the airspaces that are distal to the terminal bronchioles. This is accompanied by destruction of the airspace walls, without obvious fibro... --CHILD--> [CA21.1] Panlobular emphysema Def: Panlobular (panacinar) emphysema destroys the entire alveolus uniformly and is predominant in the lower half of the lungs. Panlobular emphysema generally is observed in patients with homozygous alpha1... --- Walk 3 --- [CA21.Z] Emphysema, unspecified --PARENT--> [CA21] Emphysema Def: Emphysema is defined by abnormal and permanent enlargement of the airspaces that are distal to the terminal bronchioles. This is accompanied by destruction of the airspace walls, without obvious fibro... --CHILD--> [CA21.0] MacLeod syndrome Def: Decrease in size of one lung due to obliterating bronchiolitis, a congenital abnormality of other disorder resulting in hyperinflation of the normal lung.... --- Walk 4 --- [CA21.Z] Emphysema, unspecified --PARENT--> [CA21] Emphysema Def: Emphysema is defined by abnormal and permanent enlargement of the airspaces that are distal to the terminal bronchioles. This is accompanied by destruction of the airspace walls, without obvious fibro... --CHILD--> [CA21.0] MacLeod syndrome Def: Decrease in size of one lung due to obliterating bronchiolitis, a congenital abnormality of other disorder resulting in hyperinflation of the normal lung.... --- Walk 5 --- [9C21.Y] Other specified endophthalmitis --PARENT--> [9C21] Endophthalmitis --CHILD--> [9C21.Y] Other specified endophthalmitis --- Walk 6 --- [9C21.Y] Other specified endophthalmitis --PARENT--> [9C21] Endophthalmitis --RELATED_TO--> [?] Purulent endophthalmitis Def: Suppurative inflammation of the tissues of the internal structures of the eye; often caused by fungi, necrosis of intraocular tumours, or retained intraocular foreign bodies. Other aetiology can be an...
[ "[CA21.Y] Other specified emphysema\n --PARENT--> [CA21] Emphysema\n Def: Emphysema is defined by abnormal and permanent enlargement of the airspaces that are distal to the terminal bronchioles. This is accompanied by destruction of the airspace walls, without obvious fibro...\n --CHILD--> [CA21.1] Panlobular emphysema\n Def: Panlobular (panacinar) emphysema destroys the entire alveolus uniformly and is predominant in the lower half of the lungs. Panlobular emphysema generally is observed in patients with homozygous alpha1...", "[CA21.Y] Other specified emphysema\n --PARENT--> [CA21] Emphysema\n Def: Emphysema is defined by abnormal and permanent enlargement of the airspaces that are distal to the terminal bronchioles. This is accompanied by destruction of the airspace walls, without obvious fibro...\n --CHILD--> [CA21.1] Panlobular emphysema\n Def: Panlobular (panacinar) emphysema destroys the entire alveolus uniformly and is predominant in the lower half of the lungs. Panlobular emphysema generally is observed in patients with homozygous alpha1...", "[CA21.Z] Emphysema, unspecified\n --PARENT--> [CA21] Emphysema\n Def: Emphysema is defined by abnormal and permanent enlargement of the airspaces that are distal to the terminal bronchioles. This is accompanied by destruction of the airspace walls, without obvious fibro...\n --CHILD--> [CA21.0] MacLeod syndrome\n Def: Decrease in size of one lung due to obliterating bronchiolitis, a congenital abnormality of other disorder resulting in hyperinflation of the normal lung....", "[CA21.Z] Emphysema, unspecified\n --PARENT--> [CA21] Emphysema\n Def: Emphysema is defined by abnormal and permanent enlargement of the airspaces that are distal to the terminal bronchioles. This is accompanied by destruction of the airspace walls, without obvious fibro...\n --CHILD--> [CA21.0] MacLeod syndrome\n Def: Decrease in size of one lung due to obliterating bronchiolitis, a congenital abnormality of other disorder resulting in hyperinflation of the normal lung....", "[9C21.Y] Other specified endophthalmitis\n --PARENT--> [9C21] Endophthalmitis\n --CHILD--> [9C21.Y] Other specified endophthalmitis", "[9C21.Y] Other specified endophthalmitis\n --PARENT--> [9C21] Endophthalmitis\n --RELATED_TO--> [?] Purulent endophthalmitis\n Def: Suppurative inflammation of the tissues of the internal structures of the eye; often caused by fungi, necrosis of intraocular tumours, or retained intraocular foreign bodies. Other aetiology can be an..." ]
CA21.Y
Other specified emphysema
[ { "from_icd11": "CA21.Z", "icd10_code": "J439", "icd10_title": "Emphysema, unspecified" }, { "from_icd11": "CA21.Z", "icd10_code": "J438", "icd10_title": "Other emphysema" }, { "from_icd11": "CA21.Z", "icd10_code": "J43", "icd10_title": "Emphysema" }, { "from_icd11": "LC51", "icd10_code": "Q278", "icd10_title": "Other specified congenital malformations of peripheral vascular system" }, { "from_icd11": "9A6Z", "icd10_code": "H10-H13", "icd10_title": "" }, { "from_icd11": "9A6Z", "icd10_code": "H13", "icd10_title": "" }, { "from_icd11": "9A6Z", "icd10_code": "H130", "icd10_title": "" }, { "from_icd11": "9A6Z", "icd10_code": "H132", "icd10_title": "" }, { "from_icd11": "9A6Z", "icd10_code": "H138", "icd10_title": "" }, { "from_icd11": "9A60.Z", "icd10_code": "H1089", "icd10_title": "Other conjunctivitis" }, { "from_icd11": "9A60.Z", "icd10_code": "H1032", "icd10_title": "Unspecified acute conjunctivitis, left eye" }, { "from_icd11": "9A60.Z", "icd10_code": "H10409", "icd10_title": "Unspecified chronic conjunctivitis, unspecified eye" }, { "from_icd11": "9A60.Z", "icd10_code": "H10419", "icd10_title": "Chronic giant papillary conjunctivitis, unspecified eye" }, { "from_icd11": "9A60.Z", "icd10_code": "H1031", "icd10_title": "Unspecified acute conjunctivitis, right eye" }, { "from_icd11": "9A60.Z", "icd10_code": "H1030", "icd10_title": "Unspecified acute conjunctivitis, unspecified eye" } ]
J439
Emphysema, unspecified
MB originally presented in 2004 at the age of 56, when she had been experiencing word-finding difficulties for unusual words (e.g., “matinée”, “gurkha”). Clinical examination and neuropsychological testing revealed no abnormalities at this time. However, three years later she was seen again and she now reported increasing word-finding difficulty, problems understanding words and following conversations, as well as difficulty with reading and spelling. Neuropsychological tests at this point indicated impairments in naming, verbal and non-verbal comprehension and surface dyslexia. Other aspects of cognition were preserved and she was well-oriented in time and space. An MRI scan revealed bilateral temporal lobe atrophy, particularly in the left hemisphere . A provisional diagnosis of semantic dementia was made. MB was regularly followed up over the next few years and a gradual deterioration in semantic knowledge was observed. She continued to work part-time as an auxiliary nurse for some time but retired in 2009, after finding that she was having difficulty understanding and producing the names of medical instruments. She remained an active participant in her local church group and girl guides organisation. She also participated in a number of our research studies on deficits in semantic cognition. When we discussed the possibility of her taking part in a relearning study, she was happy to take part.
3.734375
0.971191
sec[1]/sec[0]/p[1]
en
0.999997
25585251
https://doi.org/10.1016/j.neuropsychologia.2015.01.015
[ "time", "difficulty", "semantic", "part", "word", "words", "neuropsychological", "this", "understanding", "well" ]
[ { "code": "PL13.52", "title": "Incorrect timing of drug or medicament, as mode of injury" }, { "code": "QF2A", "title": "Difficulty or need for assistance with community participation" }, { "code": "MF50.1", "title": "Pollakiuria" }, { "code": "JA25.3", "title": "Eclampsia, time period unspecified" }, { "code": "KD3B.Z", "title": "Unspecified time of fetal death, cause not specified" }, { "code": "QE50.7", "title": "Personality difficulty" }, { "code": "QF2Z", "title": "Difficulty or need for assistance with unspecified activity" }, { "code": "MC1Y", "title": "Other specified symptoms or signs involving the visual system" }, { "code": "QF22", "title": "Difficulty or need for assistance with communication" }, { "code": "QF25", "title": "Difficulty or need for assistance with relationships" } ]
=== ICD-11 CODES FOUND === [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 [QF2A] Difficulty or need for assistance with community participation Also known as: Difficulty or need for assistance with community participation | difficulty with community participation | need for assistance with community participation | need for assistance with community, social and civic life | difficulty with community, social and civic life Includes: Lack of relaxation or leisure [MF50.1] Pollakiuria Also known as: Pollakiuria | pollakisuria | Daytime frequency of micturition [JA25.3] Eclampsia, time period unspecified Definition: Onset of convulsions in a woman with pre-eclampsia not attributable to other causes without a specific onset time. Also known as: Eclampsia, time period unspecified | Eclampsia NOS | eclamptic coma | eclamptic toxaemia | toxaemia with convulsions [KD3B.Z] Unspecified time of fetal death, cause not specified Also known as: Unspecified time of fetal death, cause not specified | Fetal death, cause not specified | stillbirth NOS | stillborn NOS | intrauterine fetal demise [QE50.7] Personality difficulty Definition: Personality difficulty refers to pronounced personality characteristics that may affect treatment or health services but do not rise to the level of severity to merit a diagnosis of Personality disorder. Personality difficulty is characterised by long-standing difficulties (e.g., at least 2 years), in the individual’s way of experiencing and thinking about the self, others and the world. In contrast to Personality disorders, these difficulties are manifested in cognitive and emotional experience Also known as: Personality difficulty Excludes: Personality disorder [QF2Z] Difficulty or need for assistance with unspecified activity Also known as: Difficulty or need for assistance with unspecified activity | need for assistance with activities | dependence on care provider | difficulty with activities [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 [QF22] Difficulty or need for assistance with communication Also known as: Difficulty or need for assistance with communication | communication difficulty | need for assistance with communication [QF25] Difficulty or need for assistance with relationships Also known as: Difficulty or need for assistance with relationships | difficulty with relationships | need for assistance with relationships | Difficulty or need for assistance with family relationships | Difficulty or need for assistance with formal relationships === GRAPH WALKS === --- Walk 1 --- [PL13.52] Incorrect timing of drug or medicament, as mode of injury --EXCLUDES--> [?] Delayed treatment --PARENT--> [?] Mode of injury or harm associated with other health care related causes --- Walk 2 --- [PL13.52] Incorrect timing of drug or medicament, as mode of injury --EXCLUDES--> [?] Delayed treatment --EXCLUDES--> [?] Overdose of substance, as mode of injury or harm Def: Incorrect dose - too high... --- Walk 3 --- [QF2A] Difficulty or need for assistance with community participation --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.... --CHILD--> [QF22] Difficulty or need for assistance with communication --- Walk 4 --- [QF2A] Difficulty or need for assistance with community participation --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 5 --- [MF50.1] Pollakiuria --PARENT--> [MF50] Abnormal micturition --CHILD--> [MF50.1] Pollakiuria --- Walk 6 --- [MF50.1] Pollakiuria --PARENT--> [MF50] Abnormal micturition --CHILD--> [MF50.0] Frequent micturition Def: Needing to urinate more often than normal....
[ "[PL13.52] Incorrect timing of drug or medicament, as mode of injury\n --EXCLUDES--> [?] Delayed treatment\n --PARENT--> [?] Mode of injury or harm associated with other health care related causes", "[PL13.52] Incorrect timing of drug or medicament, as mode of injury\n --EXCLUDES--> [?] Delayed treatment\n --EXCLUDES--> [?] Overdose of substance, as mode of injury or harm\n Def: Incorrect dose - too high...", "[QF2A] Difficulty or need for assistance with community participation\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 --CHILD--> [QF22] Difficulty or need for assistance with communication", "[QF2A] Difficulty or need for assistance with community participation\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", "[MF50.1] Pollakiuria\n --PARENT--> [MF50] Abnormal micturition\n --CHILD--> [MF50.1] Pollakiuria", "[MF50.1] Pollakiuria\n --PARENT--> [MF50] Abnormal micturition\n --CHILD--> [MF50.0] Frequent micturition\n Def: Needing to urinate more often than normal...." ]
PL13.52
Incorrect timing of drug or medicament, as mode of injury
[ { "from_icd11": "QF2A", "icd10_code": "Z7389", "icd10_title": "Other problems related to life management difficulty" }, { "from_icd11": "QF2A", "icd10_code": "Z7382", "icd10_title": "Dual sensory impairment" }, { "from_icd11": "QF2A", "icd10_code": "Z73", "icd10_title": "Problems related to life management difficulty" }, { "from_icd11": "QF2A", "icd10_code": "Z732", "icd10_title": "Lack of relaxation and leisure" }, { "from_icd11": "QF2A", "icd10_code": "Z738", "icd10_title": "Other problems related to life management difficulty" }, { "from_icd11": "QF2A", "icd10_code": "Z739", "icd10_title": "Problem related to life management difficulty, unspecified" }, { "from_icd11": "MF50.1", "icd10_code": "R351", "icd10_title": "Nocturia" }, { "from_icd11": "MF50.1", "icd10_code": "R358", "icd10_title": "Other polyuria" }, { "from_icd11": "MF50.1", "icd10_code": "R35", "icd10_title": "Polyuria" }, { "from_icd11": "JA25.3", "icd10_code": "O159", "icd10_title": "Eclampsia, unspecified as to time period" }, { "from_icd11": "KD3B.Z", "icd10_code": "P95", "icd10_title": "Stillbirth" }, { "from_icd11": "QE50.7", "icd10_code": "Z731", "icd10_title": "Type A behavior pattern" }, { "from_icd11": "QF2Z", "icd10_code": "Z742", "icd10_title": "Need for assistance at home and no other household member able to render care" }, { "from_icd11": "QF2Z", "icd10_code": "Z602", "icd10_title": "Problems related to living alone" }, { "from_icd11": "QF2Z", "icd10_code": "Z748", "icd10_title": "Other problems related to care provider dependency" } ]
Z7389
Other problems related to life management difficulty
At first, the radiologist was not able to puncture the cyst due to a thick capsule. The cyst was finally punctured under US control but could not be completely evacuated due to technical problems (dysfunctional guide wire). Cytology came back negative for malignant cells and was compatible with a cystic lymphangioma. Unfortunately, the puncture of the cyst did not help to relieve the patient’s symptoms. The patient then underwent a magnetic resonance imaging (MRI) to assess more precisely the location of this retroperitoneal cyst and its anatomic relations. T2-weighted turbo spin-echo MR-sequences showed a lesion compatible with a cystic lymphangioma originating from the left adrenal gland . The cystic lesion extended inferiorly to the renal vein and superiorly to the diaphragmatic pillar. Due to persisting invalidating pain, a surgical resection of this cystic lesion was proposed. The patient accepted the operation and signed the informed consent form. Figure 1 Magnetic resonance (MR) imaging of the cystic lymphangioma. Coronal (a) T2-weighted turbo spin-echo and axial (b) T1-weighted contrast-enhanced gradient-echo MR images show an ovoid left adrenal lesion (arrow). It is homogeneously hyperintense on T2-weightening (a) and hypointense on T1-weightening (b) , thus confirming the fluid content without loculation neither solid component. The thin wall surrounding the lesion is barely perceptible.
3.900391
0.969727
sec[1]/p[1]
en
0.999996
25889625
https://doi.org/10.1186/s12957-015-0490-0
[ "cystic", "lesion", "cyst", "lymphangioma", "weighted", "echo", "puncture", "compatible", "magnetic", "resonance" ]
[ { "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" }, { "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" } ]
=== ICD-11 CODES FOUND === [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 [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 === GRAPH WALKS === --- Walk 1 --- [CA25.Z] Cystic fibrosis, unspecified --PARENT--> [CA25] Cystic fibrosis Def: Cystic fibrosis (CF) is a genetic disorder characterised by the production of sweat with a high salt content and mucus secretions with an abnormal viscosity. The disease is chronic and generally progr... --PARENT--> [?] Certain lower respiratory tract diseases Def: This group refers to diseases of airways that forms the connection between the outside world and the terminal respiratory unit. Intrapulmonary airways are divided into three major groups; bronchi, mem... --- Walk 2 --- [CA25.Z] Cystic fibrosis, unspecified --PARENT--> [CA25] Cystic fibrosis Def: Cystic fibrosis (CF) is a genetic disorder characterised by the production of sweat with a high salt content and mucus secretions with an abnormal viscosity. The disease is chronic and generally progr... --CHILD--> [CA25.2] Subclinical cystic fibrosis --- Walk 3 --- [CB40.Y] Other specified diseases of the respiratory system --PARENT--> [CB40] Certain diseases of the respiratory system --RELATED_TO--> [?] Alpha-1-antitrypsin deficiency Def: Alpha-1-antitrypsin deficiency (AATD) is a genetic disorder that manifests as pulmonary emphysema, liver cirrhosis and, rarely, as the skin disease panniculitis, and is characterised by low serum leve... --- Walk 4 --- [CB40.Y] Other specified diseases of the respiratory system --PARENT--> [CB40] Certain diseases of the respiratory system --RELATED_TO--> [?] Airway obstruction in the neonate due to airway abnormality --- Walk 5 --- [GB71.0] Calculus in bladder Def: 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 charact... --EXCLUDES--> [?] Calculus of bowel segments for urinary diversion Def: 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 charact... --CHILD--> [?] Suburethral calculus --- Walk 6 --- [GB71.0] Calculus in bladder Def: 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 charact... --PARENT--> [GB71] Calculus of lower urinary tract Def: A condition of the urinary system, caused by dehydration, decreased urine volume or fluid flow rates, or increased excretion of minerals such as calcium, oxalate, magnesium, cystine, and phosphate. Th... --CHILD--> [GB71.1] Calculus in urethra Def: 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 charact...
[ "[CA25.Z] Cystic fibrosis, unspecified\n --PARENT--> [CA25] Cystic fibrosis\n Def: Cystic fibrosis (CF) is a genetic disorder characterised by the production of sweat with a high salt content and mucus secretions with an abnormal viscosity. The disease is chronic and generally progr...\n --PARENT--> [?] Certain lower respiratory tract diseases\n Def: This group refers to diseases of airways that forms the connection between the outside world and the terminal respiratory unit. Intrapulmonary airways are divided into three major groups; bronchi, mem...", "[CA25.Z] Cystic fibrosis, unspecified\n --PARENT--> [CA25] Cystic fibrosis\n Def: Cystic fibrosis (CF) is a genetic disorder characterised by the production of sweat with a high salt content and mucus secretions with an abnormal viscosity. The disease is chronic and generally progr...\n --CHILD--> [CA25.2] Subclinical cystic fibrosis", "[CB40.Y] Other specified diseases of the respiratory system\n --PARENT--> [CB40] Certain diseases of the respiratory system\n --RELATED_TO--> [?] Alpha-1-antitrypsin deficiency\n Def: Alpha-1-antitrypsin deficiency (AATD) is a genetic disorder that manifests as pulmonary emphysema, liver cirrhosis and, rarely, as the skin disease panniculitis, and is characterised by low serum leve...", "[CB40.Y] Other specified diseases of the respiratory system\n --PARENT--> [CB40] Certain diseases of the respiratory system\n --RELATED_TO--> [?] Airway obstruction in the neonate due to airway abnormality", "[GB71.0] Calculus in bladder\n Def: 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 charact...\n --EXCLUDES--> [?] Calculus of bowel segments for urinary diversion\n Def: 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 charact...\n --CHILD--> [?] Suburethral calculus", "[GB71.0] Calculus in bladder\n Def: 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 charact...\n --PARENT--> [GB71] Calculus of lower urinary tract\n Def: A condition of the urinary system, caused by dehydration, decreased urine volume or fluid flow rates, or increased excretion of minerals such as calcium, oxalate, magnesium, cystine, and phosphate. Th...\n --CHILD--> [GB71.1] Calculus in urethra\n Def: 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 charact..." ]
CA25.Z
Cystic fibrosis, unspecified
[ { "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" }, { "from_icd11": "GB71.0", "icd10_code": "N210", "icd10_title": "Calculus in bladder" }, { "from_icd11": "5A01.2", "icd10_code": "E042", "icd10_title": "Nontoxic multinodular goiter" }, { "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" } ]
E8419
Cystic fibrosis with other intestinal manifestations
One year after diagnosis, 2 mg chlorambucil was administered twice daily due to progressive lymphocytosis (163.5×10 9 cells/l with 90% lymphocytes). The WBC count and differentials had returned to the normal range following 11 months of chlorambucil treatment. However, 18 months after chlorambucil treatment, the patient developed progressive abdominal distention, which was painless, without B symptoms. Complete blood counts were as follows: Hemoglobin, 11.5 g/dl; platelet count, 106×10 9 cells/l; WBCs, 7.8×10 9 cells/l; segments, 63%; lymphocytes, 30.8%; monocytes, 5.3%; eosinophils, 0.6%; and basophils, 0.3%. The level of creatinine and albumin was 0.94 mg/dl and 3.57 g/dl, respectively. The electrocardiogram was normal and the cardiac sonography revealed adequate left ventricular function. Liver cirrhosis was excluded by abdominal sonography and the viral markers of hepatitis B and C were negative. The cells in ascites were predominantly lymphocytes (red blood cells, 1.285×10 9 cells/l; WBCs, 0.710×10 9 cells/l; neutrophils, 17%; and lymphocytes, 83%). The serum-ascites albumin gradient (SAAG) was 1.7, indicating transudative ascites. The ascites culture was negative for bacteria and tuberculosis. An abdominal CT scan showed enlarged mesenteric nodes with a progressive change of mesenteric inflammatory disease compared with the CT results at diagnosis. These findings did not exclude peritonitis.
4.070313
0.964355
sec[1]/p[1]
en
0.999996
24932257
https://doi.org/10.3892/ol.2014.2044
[ "cells", "lymphocytes", "ascites", "chlorambucil", "abdominal", "count", "blood", "wbcs", "albumin", "sonography" ]
[ { "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": "4B0Y", "title": "Other specified immune system disorders involving white cell lineages" }, { "code": "4B0Z", "title": "Immune system disorders involving white cell lineages, unspecified" }, { "code": "DA60.5", "title": "Lymphocytic gastric ulcer" }, { "code": "DA63.Y", "title": "Other specified duodenal ulcer" }, { "code": "2B30.13", "title": "Lymphocyte depleted classical Hodgkin lymphoma" } ]
=== ICD-11 CODES FOUND === [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 [4B0Y] Other specified immune system disorders involving white cell lineages Also known as: Other specified immune system disorders involving white cell lineages | Abnormalities of neutrophil morphology | Acquired disorders of neutrophil morphology | Constitutional disorders of neutrophil morphology | Congenital disorders of neutrophil morphology [4B0Z] Immune system disorders involving white cell lineages, unspecified Also known as: Immune system disorders involving white cell lineages, unspecified [DA60.5] Lymphocytic gastric ulcer Definition: Gastric ulcer caused by lymphocytic gastritis. Also known as: Lymphocytic gastric ulcer [DA63.Y] Other specified duodenal ulcer Also known as: Other specified duodenal ulcer | Lymphocytic duodenal ulcer | Duodenal ulcer due to diseases classified elsewhere | Duodenal ulcer due to coeliac disease | Duodenal ulcer due to Crohn disease [2B30.13] Lymphocyte depleted classical Hodgkin lymphoma Also known as: Lymphocyte depleted classical Hodgkin lymphoma | Hodgkin disease, lymphocytic depletion | Hodgkin lymphoma, lymphocyte depletion | Hodgkin lymphocytic depletion | Classical Hodgkin lymphoma, lymphocyte depletion, diffuse fibrosis === GRAPH WALKS === --- Walk 1 --- [MF9Y] Other specified clinical findings on examination of urine, without diagnosis --PARENT--> [?] Clinical findings on examination of urine, without diagnosis --CHILD--> [MF91] Bilirubinuria Def: Bilirubinuria means the presence of any bile pigment in the urine.... --- Walk 2 --- [MF9Y] Other specified clinical findings on examination of urine, without diagnosis --PARENT--> [?] Clinical findings on examination of urine, without diagnosis --PARENT--> [?] Symptoms, signs or clinical findings of the genitourinary system --- Walk 3 --- [5C56.20] Mucolipidosis --RELATED_TO--> [?] Wolman disease Def: Wolman disease represents the most severe manifestation of lysosomal acid lipase deficiency and can present in the fetus (hepatomegaly, ascites, calcified adrenal glands), or more typically in the fir... --PARENT--> [?] Lysosomal acid lipase deficiency Def: Lysosomal Acid Lipase (LAL) Deficiency happens when the body does not produce enough active lysosomal acid lipase (LAL or LIPA) enzyme. This enzyme plays an important role in breaking down fatty mater... --- Walk 4 --- [5C56.20] Mucolipidosis --RELATED_TO--> [?] Mucolipidosis type 4 Def: Mucolipidosis type IV (ML IV) is a lysosomal storage disease characterised clinically by psychomotor retardation and visual abnormalities including corneal clouding, retinal degeneration, or strabismu... --PARENT--> [?] Sphingolipidosis --- Walk 5 --- [3A51.1] Sickle cell disease without crisis Def: A disorder caused by a HbS mutation in the haemoglobin gene. This disorder is characterised by abnormal rigid sickle-shaped red blood cells decreasing its ability to carry oxygen. This disorder may pr... --PARENT--> [3A51] Sickle cell disorders or other haemoglobinopathies Def: Any disorder caused by a HbS mutation in the haemoglobin gene. This disorder is characterised by abnormal rigid sickle-shaped red blood cells decreasing its ability to carry oxygen. This disorder may ... --CHILD--> [3A51.0] Sickle cell trait Def: A disease caused by genetic inheritance of one abnormal allele of the haemoglobin gene. This disease does not display the severe symptoms of sickle cell disease that occurs in homozygous individuals. ... --- Walk 6 --- [3A51.1] Sickle cell disease without crisis Def: A disorder caused by a HbS mutation in the haemoglobin gene. This disorder is characterised by abnormal rigid sickle-shaped red blood cells decreasing its ability to carry oxygen. This disorder may pr... --PARENT--> [3A51] Sickle cell disorders or other haemoglobinopathies Def: Any disorder caused by a HbS mutation in the haemoglobin gene. This disorder is characterised by abnormal rigid sickle-shaped red blood cells decreasing its ability to carry oxygen. This disorder may ... --CHILD--> [3A51.1] Sickle cell disease without crisis Def: A disorder caused by a HbS mutation in the haemoglobin gene. This disorder is characterised by abnormal rigid sickle-shaped red blood cells decreasing its ability to carry oxygen. This disorder may pr...
[ "[MF9Y] Other specified clinical findings on examination of urine, without diagnosis\n --PARENT--> [?] Clinical findings on examination of urine, without diagnosis\n --CHILD--> [MF91] Bilirubinuria\n Def: Bilirubinuria means the presence of any bile pigment in the urine....", "[MF9Y] Other specified clinical findings on examination of urine, without diagnosis\n --PARENT--> [?] Clinical findings on examination of urine, without diagnosis\n --PARENT--> [?] Symptoms, signs or clinical findings of the genitourinary system", "[5C56.20] Mucolipidosis\n --RELATED_TO--> [?] Wolman disease\n Def: Wolman disease represents the most severe manifestation of lysosomal acid lipase deficiency and can present in the fetus (hepatomegaly, ascites, calcified adrenal glands), or more typically in the fir...\n --PARENT--> [?] Lysosomal acid lipase deficiency\n Def: Lysosomal Acid Lipase (LAL) Deficiency happens when the body does not produce enough active lysosomal acid lipase (LAL or LIPA) enzyme. This enzyme plays an important role in breaking down fatty mater...", "[5C56.20] Mucolipidosis\n --RELATED_TO--> [?] Mucolipidosis type 4\n Def: Mucolipidosis type IV (ML IV) is a lysosomal storage disease characterised clinically by psychomotor retardation and visual abnormalities including corneal clouding, retinal degeneration, or strabismu...\n --PARENT--> [?] Sphingolipidosis", "[3A51.1] Sickle cell disease without crisis\n Def: A disorder caused by a HbS mutation in the haemoglobin gene. This disorder is characterised by abnormal rigid sickle-shaped red blood cells decreasing its ability to carry oxygen. This disorder may pr...\n --PARENT--> [3A51] Sickle cell disorders or other haemoglobinopathies\n Def: Any disorder caused by a HbS mutation in the haemoglobin gene. This disorder is characterised by abnormal rigid sickle-shaped red blood cells decreasing its ability to carry oxygen. This disorder may ...\n --CHILD--> [3A51.0] Sickle cell trait\n Def: A disease caused by genetic inheritance of one abnormal allele of the haemoglobin gene. This disease does not display the severe symptoms of sickle cell disease that occurs in homozygous individuals. ...", "[3A51.1] Sickle cell disease without crisis\n Def: A disorder caused by a HbS mutation in the haemoglobin gene. This disorder is characterised by abnormal rigid sickle-shaped red blood cells decreasing its ability to carry oxygen. This disorder may pr...\n --PARENT--> [3A51] Sickle cell disorders or other haemoglobinopathies\n Def: Any disorder caused by a HbS mutation in the haemoglobin gene. This disorder is characterised by abnormal rigid sickle-shaped red blood cells decreasing its ability to carry oxygen. This disorder may ...\n --CHILD--> [3A51.1] Sickle cell disease without crisis\n Def: A disorder caused by a HbS mutation in the haemoglobin gene. This disorder is characterised by abnormal rigid sickle-shaped red blood cells decreasing its ability to carry oxygen. This disorder may pr..." ]
MF9Y
Other specified clinical findings on examination of urine, without diagnosis
[ { "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]" }, { "from_icd11": "4B0Z", "icd10_code": "D72829", "icd10_title": "Elevated white blood cell count, unspecified" }, { "from_icd11": "4B0Z", "icd10_code": "D72819", "icd10_title": "Decreased white blood cell count, unspecified" }, { "from_icd11": "4B0Z", "icd10_code": "D72818", "icd10_title": "Other decreased white blood cell count" }, { "from_icd11": "4B0Z", "icd10_code": "D72828", "icd10_title": "Other elevated white blood cell count" }, { "from_icd11": "4B0Z", "icd10_code": "D72823", "icd10_title": "Leukemoid reaction" }, { "from_icd11": "4B0Z", "icd10_code": "D72821", "icd10_title": "Monocytosis (symptomatic)" }, { "from_icd11": "4B0Z", "icd10_code": "D72825", "icd10_title": "Bandemia" }, { "from_icd11": "4B0Z", "icd10_code": "D72810", "icd10_title": "Lymphocytopenia" }, { "from_icd11": "4B0Z", "icd10_code": "D7289", "icd10_title": "Other specified disorders of white blood cells" }, { "from_icd11": "4B0Z", "icd10_code": "D72820", "icd10_title": "Lymphocytosis (symptomatic)" }, { "from_icd11": "4B0Z", "icd10_code": "D72824", "icd10_title": "Basophilia" } ]
D571
Sickle-cell disease without crisis
Its use as a device for enteral feeding and medication administration has not been previously reported in the literature. While typically a naso-gastric or oro-gastric feeding tube may be placed in patients for enteral feeding, the decision was made to leave the MT in place for two purposes. The first purpose was in case repeat tamponade was needed for recurrent massive GI bleeding. The second purpose was to be used as an enteral feeding and medication administration device. A second MT was obtained, and our nursing team was able to demonstrate and easily connect the gastric suction port to the Kangaroo enteral feeding pump . A trial of feeding was performed with the second tube, and it tolerated increasing volumes with no resistance or machine alarming noted. It was noted that the “appendix” of the tube may hold onto crushed medications, causing concern that the patient may inadvertently obtain a “bolus” of medication that could potentially cause harm. We determined that 40cc of free water flushes after the administration of medication was satisfactory without leaving any medication stuck in the MT’s appendix. This demonstration using the second tube allowed the team to feel comfortable using the first tube already in the patient. Examination of the tube after it was removed during the liver transplant showed that it had remained intact, with no breakdown, clots, or medications stuck in the tube.
3.908203
0.849609
sec[2]/p[1]
en
0.999997
PMC10110406
https://doi.org/10.7759/cureus.36340
[ "tube", "feeding", "medication", "that", "enteral", "administration", "gastric", "device", "purpose", "team" ]
[ { "code": "GA07.Z&XA3EF0", "title": "Inflammatory disease of fallopian tube" }, { "code": "JA01.1", "title": "Tubal pregnancy" }, { "code": "GB90.Y", "title": "Other specified disorders of kidney or ureter" }, { "code": "GB54", "title": "Tubulo-interstitial nephritis, not specified as acute or chronic" }, { "code": "AB10.Z", "title": "Disorders of Eustachian tube, unspecified" }, { "code": "MG43.3Z", "title": "Feeding difficulties, unspecified" }, { "code": "MG43.32", "title": "Feeding problem of adult" }, { "code": "MG43.31", "title": "Feeding problem of child" }, { "code": "6B8Z", "title": "Feeding or eating disorders, unspecified" }, { "code": "MG43.30", "title": "Feeding problem of infant" } ]
=== ICD-11 CODES FOUND === [JA01.1] Tubal pregnancy Definition: A condition characterised by implantation of the embryo within the fallopian tube (ampullary, isthmus, interstitium) during pregnancy. Also known as: Tubal pregnancy | Fallopian pregnancy | fallopian tube pregnancy | Tubal abortion | Rupture of fallopian tube due to pregnancy Includes: Fallopian pregnancy | Tubal abortion [GB90.Y] Other specified disorders of kidney or ureter Also known as: Other specified disorders of kidney or ureter | Other secondary disorders of kidney or ureter | Other disorders of kidney and ureter NEC | Inflammatory diseases of the renal pelvis or the ureter without tubulo-interstitial nephritis | Infectious diseases of the renal pelvis or the ureter without tubulo-interstitial nephritis [GB54] Tubulo-interstitial nephritis, not specified as acute or chronic Definition: A disease characterised by inflammation of and damage to tubules or the interstitium of the kidney while sparing the glomeruli secondary to immune reaction or toxic agent. Also known as: Tubulo-interstitial nephritis, not specified as acute or chronic | tubulo-interstitial nephritis | renal disease with interstitial nephritis | Congenital pyelitis | Cystopyelitis Excludes: calculous pyelonephritis [AB10.Z] Disorders of Eustachian tube, unspecified Also known as: Disorders of Eustachian tube, unspecified | Disorders of Eustachian tube | auditory tube disorder | disease of Eustachian tube | Eustachian tube dysfunction [MG43.3Z] Feeding difficulties, unspecified Also known as: Feeding difficulties, unspecified | Feeding difficulties | difficult feeding | faulty feeding | Feeding difficulties and mismanagement [MG43.32] Feeding problem of adult Also known as: Feeding problem of adult Excludes: Anorexia Nervosa | Bulimia Nervosa | Binge eating disorder [MG43.31] Feeding problem of child Also known as: Feeding problem of child Excludes: Feeding or eating disorders | Anorexia Nervosa | Avoidant-restrictive food intake disorder [6B8Z] Feeding or eating disorders, unspecified Also known as: Feeding or eating disorders, unspecified | Eating disorder, not elsewhere classified | eating disorder NOS [MG43.30] Feeding problem of infant Also known as: Feeding problem of infant Excludes: Feeding problems of newborn | Avoidant-restrictive food intake disorder === GRAPH WALKS === --- Walk 1 --- [JA01.1] Tubal pregnancy Def: A condition characterised by implantation of the embryo within the fallopian tube (ampullary, isthmus, interstitium) during pregnancy.... --PARENT--> [JA01] Ectopic pregnancy Def: Any condition characterised by implantation of the embryo outside the endometrium and endometrial cavity during pregnancy.... --CHILD--> [JA01.0] Abdominal pregnancy Def: A condition characterised by implantation of the embryo within the peritoneal cavity during pregnancy.... --- Walk 2 --- [JA01.1] Tubal pregnancy Def: A condition characterised by implantation of the embryo within the fallopian tube (ampullary, isthmus, interstitium) during pregnancy.... --PARENT--> [JA01] Ectopic pregnancy Def: Any condition characterised by implantation of the embryo outside the endometrium and endometrial cavity during pregnancy.... --CHILD--> [JA01.0] Abdominal pregnancy Def: A condition characterised by implantation of the embryo within the peritoneal cavity during pregnancy.... --- Walk 3 --- [GB90.Y] Other specified disorders of kidney or ureter --PARENT--> [GB90] Certain specified disorders of kidney or ureter Def: Any disorder characterised by pathological changes to the kidney or ureter.... --CHILD--> [GB90.2] Ureteral kinking or deviation without obstruction Def: A condition characterised by a sharp twist, curve, or other deviation in the length of the ureter, but without an obstructed flow of urine.... --- Walk 4 --- [GB90.Y] Other specified disorders of kidney or ureter --PARENT--> [GB90] Certain specified disorders of kidney or ureter Def: Any disorder characterised by pathological changes to the kidney or ureter.... --RELATED_TO--> [?] Postinterventional ischemia or infarction of kidney Def: This refers to a restriction in blood supply to tissues of the kidney due to a health care intervention causing a shortage of oxygen and glucose needed for cellular metabolism resulting in the death o... --- Walk 5 --- [GB54] Tubulo-interstitial nephritis, not specified as acute or chronic Def: A disease characterised by inflammation of and damage to tubules or the interstitium of the kidney while sparing the glomeruli secondary to immune reaction or toxic agent.... --PARENT--> [?] Renal tubulo-interstitial diseases Def: Any disease characterised by pathological changes to the renal tubules and interstitial tissues.... --RELATED_TO--> [?] Renal tubulo-interstitial disorders due to salmonella infection --- Walk 6 --- [GB54] Tubulo-interstitial nephritis, not specified as acute or chronic Def: A disease characterised by inflammation of and damage to tubules or the interstitium of the kidney while sparing the glomeruli secondary to immune reaction or toxic agent.... --EXCLUDES--> [?] Calculus of upper urinary tract Def: A condition of the urinary system, caused by dehydration, decreased urine volume or fluid flow rates, or increased excretion of minerals such as calcium, oxalate, magnesium, cystine, and phosphate. Th... --CHILD--> [?] Calculus of ureter Def: A condition of the ureter, caused by dehydration, decreased urine volume or fluid flow rates, or increased excretion of minerals such as calcium, oxalate, magnesium, cystine, and phosphate. This condi...
[ "[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--> [JA01.0] Abdominal pregnancy\n Def: A condition characterised by implantation of the embryo within the peritoneal cavity during pregnancy....", "[JA01.1] Tubal pregnancy\n Def: A condition characterised by implantation of the embryo within the fallopian tube (ampullary, isthmus, interstitium) during pregnancy....\n --PARENT--> [JA01] Ectopic pregnancy\n Def: Any condition characterised by implantation of the embryo outside the endometrium and endometrial cavity during pregnancy....\n --CHILD--> [JA01.0] Abdominal pregnancy\n Def: A condition characterised by implantation of the embryo within the peritoneal cavity during pregnancy....", "[GB90.Y] Other specified disorders of kidney or ureter\n --PARENT--> [GB90] Certain specified disorders of kidney or ureter\n Def: Any disorder characterised by pathological changes to the kidney or ureter....\n --CHILD--> [GB90.2] Ureteral kinking or deviation without obstruction\n Def: A condition characterised by a sharp twist, curve, or other deviation in the length of the ureter, but without an obstructed flow of urine....", "[GB90.Y] Other specified disorders of kidney or ureter\n --PARENT--> [GB90] Certain specified disorders of kidney or ureter\n Def: Any disorder characterised by pathological changes to the kidney or ureter....\n --RELATED_TO--> [?] Postinterventional ischemia or infarction of kidney\n Def: This refers to a restriction in blood supply to tissues of the kidney due to a health care intervention causing a shortage of oxygen and glucose needed for cellular metabolism resulting in the death o...", "[GB54] Tubulo-interstitial nephritis, not specified as acute or chronic\n Def: A disease characterised by inflammation of and damage to tubules or the interstitium of the kidney while sparing the glomeruli secondary to immune reaction or toxic agent....\n --PARENT--> [?] Renal tubulo-interstitial diseases\n Def: Any disease characterised by pathological changes to the renal tubules and interstitial tissues....\n --RELATED_TO--> [?] Renal tubulo-interstitial disorders due to salmonella infection", "[GB54] Tubulo-interstitial nephritis, not specified as acute or chronic\n Def: A disease characterised by inflammation of and damage to tubules or the interstitium of the kidney while sparing the glomeruli secondary to immune reaction or toxic agent....\n --EXCLUDES--> [?] Calculus of upper urinary tract\n Def: A condition of the urinary system, caused by dehydration, decreased urine volume or fluid flow rates, or increased excretion of minerals such as calcium, oxalate, magnesium, cystine, and phosphate. Th...\n --CHILD--> [?] Calculus of ureter\n Def: A condition of the ureter, caused by dehydration, decreased urine volume or fluid flow rates, or increased excretion of minerals such as calcium, oxalate, magnesium, cystine, and phosphate. This condi..." ]
GA07.Z&XA3EF0
Inflammatory disease of fallopian tube
[ { "from_icd11": "JA01.1", "icd10_code": "O00102", "icd10_title": "Left tubal pregnancy without intrauterine pregnancy" }, { "from_icd11": "JA01.1", "icd10_code": "O0010", "icd10_title": "Tubal pregnancy without intrauterine pregnancy" }, { "from_icd11": "JA01.1", "icd10_code": "O00101", "icd10_title": "Right tubal pregnancy without intrauterine pregnancy" }, { "from_icd11": "JA01.1", "icd10_code": "O00111", "icd10_title": "Right tubal pregnancy with intrauterine pregnancy" }, { "from_icd11": "JA01.1", "icd10_code": "O001", "icd10_title": "Tubal pregnancy" }, { "from_icd11": "GB54", "icd10_code": "N12", "icd10_title": "Tubulo-interstitial nephritis, not specified as acute or chronic" }, { "from_icd11": "AB10.Z", "icd10_code": "H6991", "icd10_title": "Unspecified Eustachian tube disorder, right ear" }, { "from_icd11": "AB10.Z", "icd10_code": "H6981", "icd10_title": "Other specified disorders of Eustachian tube, right ear" }, { "from_icd11": "AB10.Z", "icd10_code": "H6980", "icd10_title": "Other specified disorders of Eustachian tube, unspecified ear" }, { "from_icd11": "AB10.Z", "icd10_code": "H6982", "icd10_title": "Other specified disorders of Eustachian tube, left ear" }, { "from_icd11": "AB10.Z", "icd10_code": "H6990", "icd10_title": "Unspecified Eustachian tube disorder, unspecified ear" }, { "from_icd11": "AB10.Z", "icd10_code": "H68", "icd10_title": "Eustachian salpingitis and obstruction" }, { "from_icd11": "AB10.Z", "icd10_code": "H69", "icd10_title": "Other and unspecified disorders of Eustachian tube" }, { "from_icd11": "AB10.Z", "icd10_code": "H698", "icd10_title": "Other specified disorders of Eustachian tube" }, { "from_icd11": "AB10.Z", "icd10_code": "H699", "icd10_title": "Unspecified Eustachian tube disorder" } ]
O00102
Left tubal pregnancy without intrauterine pregnancy
We believe that this case report is of great interest because our patient contemporarily developed two community-onset healthcare associated infections with a rapidly fatal outcome. Carbapenem-resistant Enterobacteriaceae (CRE) are an emerging issue of great public health concern. In our country, the problem is almost completely represented by carbapenem-resistant K. pneumoniae . Even though data related to incidence are missing, percentage of invasive K. pneumoniae isolates with resistance to carbapenems reportedly ranges between 25% and 50% in Italy . Recently, cases of healthcare-associated carbapenem resistant K. pneumoniae BSIs have been reported in Northern Italy . The phenomenon is also well known in Rome and parallels to an epidemiological shift of CDI occurring in our region and consisting of increased disease incidence and mortality rates , that are probably due to the spread of the epidemic strain ribotype 027 CD [ 6 – 8 ]. In the present case, because the initial diagnosis was made in a peripheral center, ribotyping test was not performed. We describe, for the first time, a fatal case of severe CDI complicated by KPC-Kp BSI. This led us to question about the role of severe CDI on predisposing to HCA-BSIs, and vice-versa, on the role of HCA-BSIs in determining the prognosis of severe CD colitis. To our knowledge this issue has never been thoroughly evaluated in the literature until now.
4.132813
0.883789
sec[2]/p[0]
en
0.999995
25178451
https://doi.org/10.1186/1471-2334-14-475
[ "this", "carbapenem", "resistant", "pneumoniae", "bsis", "that", "great", "because", "associated", "fatal" ]
[ { "code": "4A01.03", "title": "Transient hypogammaglobulinaemia of infancy" }, { "code": "MG50.92", "title": "Carbapenem resistant Salmonella" }, { "code": "MG50.A0", "title": "Carbapenem resistant Shigella" }, { "code": "MG50.C0", "title": "Other carbapenem resistant Enterobacterales" }, { "code": "MG50.02", "title": "Carbapenem resistant Acinetobacter baumannii" }, { "code": "MG50.54", "title": "Carbapenem resistant Klebsiella pneumoniae" }, { "code": "MG55.0", "title": "Artemisinin resistant Plasmodium falciparum" }, { "code": "5A74.Y", "title": "Other specified adrenocortical insufficiency" }, { "code": "5A44", "title": "Insulin-resistance syndromes" }, { "code": "LD2A.4", "title": "46,XY disorder of sex development due to androgen resistance" } ]
=== ICD-11 CODES FOUND === [4A01.03] Transient hypogammaglobulinaemia of infancy Also known as: Transient hypogammaglobulinaemia of infancy | immunoglobulin maturational delay | THI - [transient hypogammaglobulinaemia of infancy] [MG50.92] Carbapenem resistant Salmonella Also known as: Carbapenem resistant Salmonella | Doripenem resistant Salmonella | Ertapenem resistant Salmonella | Imipenem resistant Salmonella | Meropenem resistant Salmonella [MG50.A0] Carbapenem resistant Shigella Also known as: Carbapenem resistant Shigella [MG50.C0] Other carbapenem resistant Enterobacterales Also known as: Other carbapenem resistant Enterobacterales [MG50.02] Carbapenem resistant Acinetobacter baumannii Also known as: Carbapenem resistant Acinetobacter baumannii | Doripenem resistant Acinetobacter baumannii | Imipenem resistant Acinetobacter baumannii | Meropenem resistant Acinetobacter baumannii [MG50.54] Carbapenem resistant Klebsiella pneumoniae Also known as: Carbapenem resistant Klebsiella pneumoniae | Doripenem resistant Klebsiella pneumoniae | Ertapenem resistant Klebsiella pneumoniae | Imipenem resistant Klebsiella pneumoniae | Meropenem resistant Klebsiella pneumoniae [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 [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 [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 [LD2A.4] 46,XY disorder of sex development due to androgen resistance Definition: Androgen insensitivity syndrome (AIS) is a disorder of sex development (DSD) characterised by the presence of female external genitalia, ambiguous genitalia or variable defects in virilization in a 46,XY individual with absent or partial responsiveness to age-appropriate levels of androgens. It comprises two clinical subgroups: complete AIS (CAIS) and partial AIS (PAIS). Also known as: 46,XY disorder of sex development due to androgen resistance | Androgen resistance syndrome | Testicular feminization syndrome | Androgen insensitivity syndrome | Goldberg-Maxwell syndrome === GRAPH WALKS === --- Walk 1 --- [4A01.03] Transient hypogammaglobulinaemia of infancy --PARENT--> [4A01.0] Immunodeficiencies with predominantly antibody defects Def: A disorder characterised by an inability to mount a normal immune response due to antibody (i.e. immunoglobulin) defects... --CHILD--> [4A01.00] Hereditary agammaglobulinaemia with profoundly reduced or absent B cells Def: This refers to a hereditary type of primary immune deficiency disease characterised by a reduction in all types of gamma globulins, and rare X-linked genetic disorder that affects the body's ability t... --- Walk 2 --- [4A01.03] Transient hypogammaglobulinaemia of infancy --PARENT--> [4A01.0] Immunodeficiencies with predominantly antibody defects Def: A disorder characterised by an inability to mount a normal immune response due to antibody (i.e. immunoglobulin) defects... --CHILD--> [4A01.00] Hereditary agammaglobulinaemia with profoundly reduced or absent B cells Def: This refers to a hereditary type of primary immune deficiency disease characterised by a reduction in all types of gamma globulins, and rare X-linked genetic disorder that affects the body's ability t... --- Walk 3 --- [MG50.92] Carbapenem resistant Salmonella --PARENT--> [MG50.9] Antibiotic resistant Salmonella --CHILD--> [MG50.90] Fluoroquinolone resistant Salmonella --- Walk 4 --- [MG50.92] Carbapenem resistant Salmonella --PARENT--> [MG50.9] Antibiotic resistant Salmonella --CHILD--> [MG50.90] Fluoroquinolone resistant Salmonella --- Walk 5 --- [MG50.A0] Carbapenem resistant Shigella --PARENT--> [MG50.A] Antibiotic resistant Shigella --CHILD--> [MG50.A1] Fluoroquinolone resistant Shigella --- Walk 6 --- [MG50.A0] Carbapenem resistant Shigella --PARENT--> [MG50.A] Antibiotic resistant Shigella --CHILD--> [MG50.A2] Third-generation cephalosporins resistant Shigella
[ "[4A01.03] Transient hypogammaglobulinaemia of infancy\n --PARENT--> [4A01.0] Immunodeficiencies with predominantly antibody defects\n Def: A disorder characterised by an inability to mount a normal immune response due to antibody (i.e. immunoglobulin) defects...\n --CHILD--> [4A01.00] Hereditary agammaglobulinaemia with profoundly reduced or absent B cells\n Def: This refers to a hereditary type of primary immune deficiency disease characterised by a reduction in all types of gamma globulins, and rare X-linked genetic disorder that affects the body's ability t...", "[4A01.03] Transient hypogammaglobulinaemia of infancy\n --PARENT--> [4A01.0] Immunodeficiencies with predominantly antibody defects\n Def: A disorder characterised by an inability to mount a normal immune response due to antibody (i.e. immunoglobulin) defects...\n --CHILD--> [4A01.00] Hereditary agammaglobulinaemia with profoundly reduced or absent B cells\n Def: This refers to a hereditary type of primary immune deficiency disease characterised by a reduction in all types of gamma globulins, and rare X-linked genetic disorder that affects the body's ability t...", "[MG50.92] Carbapenem resistant Salmonella\n --PARENT--> [MG50.9] Antibiotic resistant Salmonella\n --CHILD--> [MG50.90] Fluoroquinolone resistant Salmonella", "[MG50.92] Carbapenem resistant Salmonella\n --PARENT--> [MG50.9] Antibiotic resistant Salmonella\n --CHILD--> [MG50.90] Fluoroquinolone resistant Salmonella", "[MG50.A0] Carbapenem resistant Shigella\n --PARENT--> [MG50.A] Antibiotic resistant Shigella\n --CHILD--> [MG50.A1] Fluoroquinolone resistant Shigella", "[MG50.A0] Carbapenem resistant Shigella\n --PARENT--> [MG50.A] Antibiotic resistant Shigella\n --CHILD--> [MG50.A2] Third-generation cephalosporins resistant Shigella" ]
4A01.03
Transient hypogammaglobulinaemia of infancy
[ { "from_icd11": "4A01.03", "icd10_code": "D807", "icd10_title": "Transient hypogammaglobulinemia of infancy" }, { "from_icd11": "MG50.02", "icd10_code": "U828", "icd10_title": "" }, { "from_icd11": "5A44", "icd10_code": "E10-E14", "icd10_title": "" }, { "from_icd11": "LD2A.4", "icd10_code": "E3450", "icd10_title": "Androgen insensitivity syndrome, unspecified" }, { "from_icd11": "LD2A.4", "icd10_code": "E3451", "icd10_title": "Complete androgen insensitivity syndrome" }, { "from_icd11": "LD2A.4", "icd10_code": "E345", "icd10_title": "Androgen insensitivity syndrome" } ]
D807
Transient hypogammaglobulinemia of infancy
A 42-year-old woman presented to the emergency department with a two-day history of fever (39℃), chills, loss of appetite, right-sided abdominal distention, and pain extending from the right side of the abdomen to the back. No signs of cystitis, such as dysuria, frequent or urgent urination, or hematuria, were observed. She had undergone discectomy for a herniated lumbar L4/L5 disc six years prior to presentation. Her current medications included pregabalin, etodolac, rebamipide, and etizolam. She was regularly using nonsteroidal anti-inflammatory drugs due to severe postoperative pain. Her temperature was 38.5℃, pulse rate was 92 beats/min, blood pressure was 110/68 mmHg, and SpO 2 was 98% (room air). Physical examination revealed soft, non-tender abdomen without costovertebral angle tenderness. Blood test and urinalysis results are shown in Table 1 . Abdominal ultrasonography revealed a 32 × 25 mm nodular shadow on the upper pole of the right kidney . The nodule had irregular margins and indistinct borders, and its interior had a mosaic-like echogenic appearance. Contrast-enhanced computed tomography (CT) of the abdomen revealed a wedge-shaped partially contrast-impaired area in the right kidney . The patient was admitted to the hospital, and tazobactam/piperacillin was administered. No other causes for her fever were found, and AFBN was suspected based on the clinical and radiological findings.
3.769531
0.98584
sec[1]/p[0]
en
0.999997
PMC9874170
https://doi.org/10.7759/cureus.32942
[ "abdomen", "fever", "abdominal", "pain", "blood", "kidney", "contrast", "emergency", "department", "chills" ]
[ { "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": "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" } ]
=== 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 [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 === GRAPH WALKS === --- Walk 1 --- [MD81.3] Acute abdomen Def: A clinical syndrome with acute abdominal pain that is severe, and rapid onset. Acute abdomen may be caused by a variety of disorders, injuries, or diseases... --PARENT--> [MD81] Abdominal or pelvic pain Def: Pain, an unpleasant distress sensation occurring in varying degrees of severity, received by nerve ending in the abdominal and pelvic region.... --EXCLUDES--> [?] Spinal pain Def: This is a condition characterised by pain felt in the back that usually originates from the muscles, nerves, bones, joints or other structures in the spine.... --- Walk 2 --- [MD81.3] Acute abdomen Def: A clinical syndrome with acute abdominal pain that is severe, and rapid onset. Acute abdomen may be caused by a variety of disorders, injuries, or diseases... --PARENT--> [MD81] Abdominal or pelvic pain Def: Pain, an unpleasant distress sensation occurring in varying degrees of severity, received by nerve ending in the abdominal and pelvic region.... --EXCLUDES--> [?] Spinal pain Def: This is a condition characterised by pain felt in the back that usually originates from the muscles, nerves, bones, joints or other structures in the spine.... --- Walk 3 --- [JA01.0] Abdominal pregnancy Def: A condition characterised by implantation of the embryo within the peritoneal cavity during pregnancy.... --EXCLUDES--> [?] Delivery of viable fetus in abdominal pregnancy Def: A condition caused by the development of a viable fetus to the culmination of the pregnancy period. This condition is characterised by parturition of a viable neonate from the abdominal cavity, at the... --PARENT--> [?] Other assisted single delivery --- Walk 4 --- [JA01.0] Abdominal pregnancy Def: A condition characterised by implantation of the embryo within the peritoneal cavity during pregnancy.... --PARENT--> [JA01] Ectopic pregnancy Def: Any condition characterised by implantation of the embryo outside the endometrium and endometrial cavity during pregnancy.... --CHILD--> [JA01.2] Ovarian pregnancy Def: A condition characterised by implantation of the embryo within the ovary during pregnancy.... --- Walk 5 --- [ME04.Z] Ascites, unspecified --PARENT--> [ME04] Ascites Def: Accumulation or retention of free fluid in the abdominal peritoneal cavity between the tissues lining the abdomen and abdominal organs. The fluid may be serous, haemorrhagic, or the result of inflamma... --CHILD--> [ME04.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--> [ME04.0] Fluid in peritoneal cavity
[ "[MD81.3] Acute abdomen\n Def: A clinical syndrome with acute abdominal pain that is severe, and rapid onset. Acute abdomen may be caused by a variety of disorders, injuries, or diseases...\n --PARENT--> [MD81] Abdominal or pelvic pain\n Def: Pain, an unpleasant distress sensation occurring in varying degrees of severity, received by nerve ending in the abdominal and pelvic region....\n --EXCLUDES--> [?] Spinal pain\n Def: This is a condition characterised by pain felt in the back that usually originates from the muscles, nerves, bones, joints or other structures in the spine....", "[MD81.3] Acute abdomen\n Def: A clinical syndrome with acute abdominal pain that is severe, and rapid onset. Acute abdomen may be caused by a variety of disorders, injuries, or diseases...\n --PARENT--> [MD81] Abdominal or pelvic pain\n Def: Pain, an unpleasant distress sensation occurring in varying degrees of severity, received by nerve ending in the abdominal and pelvic region....\n --EXCLUDES--> [?] Spinal pain\n Def: This is a condition characterised by pain felt in the back that usually originates from the muscles, nerves, bones, joints or other structures in the spine....", "[JA01.0] Abdominal pregnancy\n Def: A condition characterised by implantation of the embryo within the peritoneal cavity during pregnancy....\n --EXCLUDES--> [?] Delivery of viable fetus in abdominal pregnancy\n Def: A condition caused by the development of a viable fetus to the culmination of the pregnancy period. This condition is characterised by parturition of a viable neonate from the abdominal cavity, at the...\n --PARENT--> [?] Other assisted single delivery", "[JA01.0] Abdominal pregnancy\n Def: A condition characterised by implantation of the embryo within the peritoneal cavity during pregnancy....\n --PARENT--> [JA01] Ectopic pregnancy\n Def: Any condition characterised by implantation of the embryo outside the endometrium and endometrial cavity during pregnancy....\n --CHILD--> [JA01.2] Ovarian pregnancy\n Def: A condition characterised by implantation of the embryo within the ovary during pregnancy....", "[ME04.Z] Ascites, unspecified\n --PARENT--> [ME04] Ascites\n Def: Accumulation or retention of free fluid in the abdominal peritoneal cavity between the tissues lining the abdomen and abdominal organs. The fluid may be serous, haemorrhagic, or the result of inflamma...\n --CHILD--> [ME04.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--> [ME04.0] Fluid in peritoneal cavity" ]
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": "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" } ]
R100
Acute abdomen
The patient was installed in a contralateral decubitus position on a ball mattress, with the table broken at a 30° angle. A Pfannenstiel incision was performed first (sometimes using a previous one in women), the Gelport ® was inserted and the pneumoperitoneum initiated (12 mmHg). The hand was introduced and secured the placement of one 12 mm trocar in the ipsilateral iliac fossa (for dissection and staplers), then an 11 mm trocar was inserted under direct vision in the ipsilateral hypochondrium (for the laparoscope). On the right side, an additional epigastric 5 mm trocar helped to retract the liver; see Fig. 1 . The rest of the procedure was similar to the abovementioned. Initially, 5000 U of heparin iv. was administered and controlled after the section of vessels by Protamin, but it was progressively abandoned without any consequence regarding morbidity. The artery was first double stapled and cut (Covidien Endo GIA™ Ultra 30 mm. vascular articulated Tri-staple™) and the vein had a simple stapling (Covidien EndoTA 30 mm. Auto Suture™ 30 mm.) and was then cut, to preserve a maximum length. The kidney was removed by hand through the Gelport ® and transferred for immediate cold perfusion. Warm ischemia time was measured precisely from vessel clamping to back table IGL-1 cooling and venous efflux. After controlling hemostasis, all incisions were closed according to the usual standardized technique.
3.886719
0.907715
sec[1]/sec[0]/sec[1]/p[0]
en
0.999995
35254601
https://doi.org/10.1007/s11701-022-01393-x
[ "trocar", "gelport", "hand", "ipsilateral", "covidien", "installed", "contralateral", "decubitus", "position", "ball" ]
[ { "code": "NC59.4", "title": "Traumatic amputation of hand at metacarpal level" }, { "code": "QF00", "title": "Acquired absence of limb" }, { "code": "MB54.Z", "title": "Monoplegia of upper extremity, unspecified" }, { "code": "FB3Z", "title": "Disorders of muscles, unspecified" }, { "code": "FB56.6", "title": "Other specified soft tissue disorders" }, { "code": "9C83.10", "title": "Horizontal conjugate gaze deviation" }, { "code": "PL12.5", "title": "Operator error, as mode of injury or harm" }, { "code": "QA64", "title": "Operator error without injury or harm" }, { "code": "EH90.Z", "title": "Pressure ulcer of unspecified grade" }, { "code": "GA15.1", "title": "Erosion or ectropion of cervix uteri" } ]
=== ICD-11 CODES FOUND === [NC59.4] Traumatic amputation of hand at metacarpal level Also known as: Traumatic amputation of hand at metacarpal level | severed hand | Traumatic amputation of left hand at metacarpal level | avulsion of left hand at metacarpal level | Traumatic amputation of right hand at metacarpal level [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 [MB54.Z] Monoplegia of upper extremity, unspecified Also known as: Monoplegia of upper extremity, unspecified | Monoplegia of upper extremity | paralysis of upper limb | monoplegia of upper limb | monoplegia of upper limb affecting unspecified side [FB3Z] Disorders of muscles, unspecified Also known as: Disorders of muscles, unspecified | disorder of muscle, unspecified | muscle disease | muscular disease | muscular disorder [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 [9C83.10] Horizontal conjugate gaze deviation Also known as: Horizontal conjugate gaze deviation | Sustained horizontal conjugate gaze deviation | Sustained horizontal conjugate gaze deviation, ipsilateral type | Sustained horizontal conjugate gaze deviation, contralateral type | Sustained tonic horizontal conjugate gaze deviation [PL12.5] Operator error, as mode of injury or harm Definition: Harm arising due to process or procedural issues associated with the use and/or maintenance of a device not related to device failure. Also known as: Operator error, as mode of injury or harm | operator error due to poor training as mode of injury | operator error due to poor maintenance as mode of injury | operator error due to incorrect device installation as mode of injury | mistake by operator Excludes: Combination or interaction of operator error and device failure, as mode of injury or harm | Operator error without injury or harm [QA64] Operator error without injury or harm Definition: Incorrect, or improper maintenance or installation of device without documented injury or harm due to operator error. Also known as: Operator error without injury or harm | Operator error due to suboptimal training without documented injury or harm | Incorrect device installation due to operator error without documented injury or harm | Suboptimal maintenance due to operator error without documented injury or harm | mistake by operator or health care provider without documented injury or harm Excludes: Operator error, as mode of injury or harm [EH90.Z] Pressure ulcer of unspecified grade Also known as: Pressure ulcer of unspecified grade | Pressure ulceration | pressure injury | pressure ulcer | decubitus ulcer [GA15.1] Erosion or ectropion of cervix uteri Definition: A condition of the cervix uteri, caused by an increase in the total estrogen level in the body. This condition is characterised by protrusion and transformation of the endocervical columnar epithelium to stratified squamous epithelium on the cervix uteri. This condition may also present with non-purulent vaginal discharge, post-coital bleeding, or may be asymptomatic. Also known as: Erosion or ectropion of cervix uteri | Cervical ectropion | cervical eversion | eversion of cervix | ectropion of cervix Excludes: Cervicitis === GRAPH WALKS === --- Walk 1 --- [NC59.4] Traumatic amputation of hand at metacarpal level --PARENT--> [NC59] Traumatic amputation of wrist or hand --PARENT--> [?] Injuries to the wrist or hand --- Walk 2 --- [NC59.4] Traumatic amputation of hand at metacarpal level --PARENT--> [NC59] Traumatic amputation of wrist or hand --CHILD--> [NC59.1] Traumatic amputation of other single finger --- Walk 3 --- [QF00] Acquired absence of limb --EXCLUDES--> [?] Other acquired deformities of limbs --CHILD--> [?] Valgus deformity, not elsewhere classified --- Walk 4 --- [QF00] Acquired absence of limb --EXCLUDES--> [?] Congenital absence of thigh or lower leg with foot present Def: Any condition caused by the failure of the thigh and lower leg to develop during the antenatal period. These conditions are characterised by direct connection of the foot to the hip.... --CHILD--> [?] Congenital absence of thigh or lower leg with foot present, bilateral --- Walk 5 --- [MB54.Z] Monoplegia of upper extremity, unspecified --PARENT--> [MB54] Monoplegia of upper extremity Def: This is a loss of motor control in one arm.... --CHILD--> [MB54.0] Flaccid monoplegia of upper extremity --- Walk 6 --- [MB54.Z] Monoplegia of upper extremity, unspecified --PARENT--> [MB54] Monoplegia of upper extremity Def: This is a loss of motor control in one arm.... --CHILD--> [MB54.Z] Monoplegia of upper extremity, unspecified
[ "[NC59.4] Traumatic amputation of hand at metacarpal level\n --PARENT--> [NC59] Traumatic amputation of wrist or hand\n --PARENT--> [?] Injuries to the wrist or hand", "[NC59.4] Traumatic amputation of hand at metacarpal level\n --PARENT--> [NC59] Traumatic amputation of wrist or hand\n --CHILD--> [NC59.1] Traumatic amputation of other single finger", "[QF00] Acquired absence of limb\n --EXCLUDES--> [?] Other acquired deformities of limbs\n --CHILD--> [?] Valgus deformity, not elsewhere classified", "[QF00] Acquired absence of limb\n --EXCLUDES--> [?] Congenital absence of thigh or lower leg with foot present\n Def: Any condition caused by the failure of the thigh and lower leg to develop during the antenatal period. These conditions are characterised by direct connection of the foot to the hip....\n --CHILD--> [?] Congenital absence of thigh or lower leg with foot present, bilateral", "[MB54.Z] Monoplegia of upper extremity, unspecified\n --PARENT--> [MB54] Monoplegia of upper extremity\n Def: This is a loss of motor control in one arm....\n --CHILD--> [MB54.0] Flaccid monoplegia of upper extremity", "[MB54.Z] Monoplegia of upper extremity, unspecified\n --PARENT--> [MB54] Monoplegia of upper extremity\n Def: This is a loss of motor control in one arm....\n --CHILD--> [MB54.Z] Monoplegia of upper extremity, unspecified" ]
NC59.4
Traumatic amputation of hand at metacarpal level
[ { "from_icd11": "QF00", "icd10_code": "Z89412", "icd10_title": "Acquired absence of left great toe" }, { "from_icd11": "QF00", "icd10_code": "Z89611", "icd10_title": "Acquired absence of right leg above knee" }, { "from_icd11": "QF00", "icd10_code": "Z89421", "icd10_title": "Acquired absence of other right toe(s)" }, { "from_icd11": "QF00", "icd10_code": "Z89431", "icd10_title": "Acquired absence of right foot" }, { "from_icd11": "QF00", "icd10_code": "Z89522", "icd10_title": "Acquired absence of left knee" }, { "from_icd11": "QF00", "icd10_code": "Z89411", "icd10_title": "Acquired absence of right great toe" }, { "from_icd11": "QF00", "icd10_code": "Z89511", "icd10_title": "Acquired absence of right leg below knee" }, { "from_icd11": "QF00", "icd10_code": "Z89429", "icd10_title": "Acquired absence of other toe(s), unspecified side" }, { "from_icd11": "QF00", "icd10_code": "Z89422", "icd10_title": "Acquired absence of other left toe(s)" }, { "from_icd11": "QF00", "icd10_code": "Z89211", "icd10_title": "Acquired absence of right upper limb below elbow" }, { "from_icd11": "QF00", "icd10_code": "Z89612", "icd10_title": "Acquired absence of left leg above knee" }, { "from_icd11": "QF00", "icd10_code": "Z89512", "icd10_title": "Acquired absence of left leg below knee" }, { "from_icd11": "QF00", "icd10_code": "Z89432", "icd10_title": "Acquired absence of left foot" }, { "from_icd11": "QF00", "icd10_code": "Z89021", "icd10_title": "Acquired absence of right finger(s)" }, { "from_icd11": "QF00", "icd10_code": "Z89419", "icd10_title": "Acquired absence of unspecified great toe" } ]
Z89412
Acquired absence of left great toe
Particularly, spinal cord infarction is very rare in postpartum ischemic stroke. From a review of the literature, only two cases have been reported until now . In 1981, Dunn reported a 26-year-old female presenting with sudden onset of deep burning pain below the chest, paraparesis and incontinence on her 20th postpartum day. The anterior spinal artery syndrome was diagnosed at that time. Hormonal effect on cerebral vascular endothelium or hyper-coagulopathy of pregnancy were suspected as possible etiologies . In 2011, Soda et al. reported a 35-year-old woman presenting with acute onset, progressive low limbs paresthesia, weakness and dysuria for 3 days on her 6th postpartum day. The thrombocytosis and high fibrinolytic activity during the peripartum period were assumed to be a cause of anterior spinal artery syndrome in this case . However, no anesthesia procedure, COVID or other vaccinations have been documented for both cases. In our case, the presentation of acute paraparesis with sensory dissociation and sphincter incontinence after normal vaginal delivery suggested postpartum anterior spinal cord infarction, which was confirmed by the imaging findings. Table 1 shows the comparison of laboratory data between previous literature and our case. A relatively lower platelet count with normal fibrinogen level was found during admission in our case, which is not compatible with the previous reports.
4.046875
0.703613
sec[2]/sec[0]/p[1]
en
0.999996
36355059
https://doi.org/10.3390/medicines9110054
[ "spinal", "postpartum", "cord", "infarction", "literature", "cases", "presenting", "onset", "paraparesis", "incontinence" ]
[ { "code": "FB1Z", "title": "Conditions associated with the spine, unspecified" }, { "code": "FA7Z", "title": "Structural disorders of spine, unspecified" }, { "code": "FA9Z", "title": "Inflammation of spine, unspecified" }, { "code": "LB73.2Z", "title": "Structural developmental anomalies of spine, unspecified" }, { "code": "FA82", "title": "Spinal stenosis" }, { "code": "JB4Z", "title": "Complications predominantly related to the puerperium, unspecified" }, { "code": "JA43.3", "title": "Postpartum coagulation defects" }, { "code": "QA48.Z", "title": "Postpartum care or examination, unspecified" }, { "code": "MF35", "title": "Postpartum symptom or complaint" }, { "code": "QA48.0", "title": "Care or examination immediately after delivery" } ]
=== ICD-11 CODES FOUND === [FB1Z] Conditions associated with the spine, unspecified Also known as: Conditions associated with the spine, unspecified | dorsopathies | disorder of spine | spinal disorder [FA7Z] Structural disorders of spine, unspecified Also known as: Structural disorders of spine, unspecified | spinal disease [FA9Z] Inflammation of spine, unspecified Also known as: Inflammation of spine, unspecified | spinal inflammation | discitis, unspecified [LB73.2Z] Structural developmental anomalies of spine, unspecified Also known as: Structural developmental anomalies of spine, unspecified | Structural developmental anomalies of spine | Malformations of spine | maldevelopment of spine [FA82] Spinal stenosis Definition: This is a condition characterised by narrowing of the spinal canal. Also known as: Spinal stenosis | spinal canal stenosis | Spinal stenosis with no determinant | primary spinal stenosis | Spinal stenosis with determinant [JB4Z] Complications predominantly related to the puerperium, unspecified Also known as: Complications predominantly related to the puerperium, unspecified | Puerperal complication NOS | disorder of puerperium | postpartum disorder [JA43.3] Postpartum coagulation defects Definition: A condition characterised by excessive loss of blood following a vaginal or caesarean section delivery. This condition is caused by coagulation defects during the postpartum period. Also known as: Postpartum coagulation defects | puerperal coagulopathy | Circulating anticoagulants following childbirth | Postpartum afibrinogenaemia | Postpartum blood dyscrasia [QA48.Z] Postpartum care or examination, unspecified Also known as: Postpartum care or examination, unspecified | Postpartum care or examination [MF35] Postpartum symptom or complaint Also known as: Postpartum symptom or complaint [QA48.0] Care or examination immediately after delivery Also known as: Care or examination immediately after delivery | care and observation in uncomplicated delivery cases | postpartum care immediately after delivery | postpartum examination immediately after delivery | Postpartum care after hospital delivery Excludes: Complications predominantly related to the puerperium === GRAPH WALKS === --- Walk 1 --- [FB1Z] Conditions associated with the spine, unspecified --PARENT--> [?] 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.... --RELATED_TO--> [?] Spinal pain Def: This is a condition characterised by pain felt in the back that usually originates from the muscles, nerves, bones, joints or other structures in the spine.... --- Walk 2 --- [FB1Z] Conditions associated with the spine, unspecified --PARENT--> [?] 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.... --CHILD--> [?] Structural disorders of spine --- Walk 3 --- [FA7Z] Structural disorders of spine, unspecified --PARENT--> [?] Structural disorders of spine --CHILD--> [FA70] Spinal deformities --- Walk 4 --- [FA7Z] Structural disorders of spine, unspecified --PARENT--> [?] Structural disorders of spine --CHILD--> [FA71] Torticollis --- Walk 5 --- [FA9Z] Inflammation of spine, unspecified --PARENT--> [?] Inflammation of spine --PARENT--> [?] 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 6 --- [FA9Z] Inflammation of spine, unspecified --PARENT--> [?] Inflammation of spine --CHILD--> [FA92] Inflammatory spondyloarthritis Def: Inflammatory spondyloarthritis is a rheumatic disease referring to the group of inflammatory disorders affecting the lower limb, enthesitis, dactylitis, and uveitis. Clinical characteristics include t...
[ "[FB1Z] Conditions associated with the spine, unspecified\n --PARENT--> [?] 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....\n --RELATED_TO--> [?] 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....", "[FB1Z] Conditions associated with the spine, unspecified\n --PARENT--> [?] 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....\n --CHILD--> [?] Structural disorders of spine", "[FA7Z] Structural disorders of spine, unspecified\n --PARENT--> [?] Structural disorders of spine\n --CHILD--> [FA70] Spinal deformities", "[FA7Z] Structural disorders of spine, unspecified\n --PARENT--> [?] Structural disorders of spine\n --CHILD--> [FA71] Torticollis", "[FA9Z] Inflammation of spine, unspecified\n --PARENT--> [?] Inflammation of spine\n --PARENT--> [?] 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....", "[FA9Z] Inflammation of spine, unspecified\n --PARENT--> [?] Inflammation of spine\n --CHILD--> [FA92] Inflammatory spondyloarthritis\n Def: Inflammatory spondyloarthritis is a rheumatic disease referring to the group of inflammatory disorders affecting the lower limb, enthesitis, dactylitis, and uveitis. Clinical characteristics include t..." ]
FB1Z
Conditions associated with the spine, unspecified
[ { "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" }, { "from_icd11": "FB1Z", "icd10_code": "M4326", "icd10_title": "Fusion of spine, lumbar region" }, { "from_icd11": "FB1Z", "icd10_code": "M438X2", "icd10_title": "Other specified deforming dorsopathies, cervical region" }, { "from_icd11": "FB1Z", "icd10_code": "M4327", "icd10_title": "Fusion of spine, lumbosacral region" }, { "from_icd11": "FB1Z", "icd10_code": "M4322", "icd10_title": "Fusion of spine, cervical region" }, { "from_icd11": "FB1Z", "icd10_code": "M4321", "icd10_title": "Fusion of spine, occipito-atlanto-axial region" }, { "from_icd11": "FB1Z", "icd10_code": "M438X9", "icd10_title": "Other specified deforming dorsopathies, site unspecified" }, { "from_icd11": "FB1Z", "icd10_code": "M4328", "icd10_title": "Fusion of spine, sacral and sacrococcygeal region" } ]
M435X2
Other recurrent vertebral dislocation, cervical region
Lung infections caused by Histoplasma are usually asymptomatic or mildly symptomatic. The severity of infection depends primarily on the amount of the initial inoculum and immune status of the host. Pulmonary infection and extrapulmonary spread resolve spontaneously in >99% of cases as cellular immunity develops. In patients who fail to mount an effective immune response, the infection is usually progressive ( 6 ). Here, we report case of a female patient with Histoplasma -associated empyema. Severe infection in this patient was associated with decreased immune function due to diabetes, gastric malignancy and probable latent TB infection suggested by the positive result of T-SPOT.TB. Pleural effusion in patients with histoplasmosis is rare, with an incidence ranging from 0 to 6% ( 7 , 8 ), although Histoplasma pneumonia usually adjoins the pleural space. Massive pleural effusion has only been reported in few cases ( 9 , 10 ). No empyema associated with Histoplasma infection has been reported to date. The pathogenic agents in the pleural fluid of this patient were Escherichia coli, Streptococcus constellation and Histoplasma . Her remission was not ideal after receiving antibacterial treatment. The purulent pleural effusion gradually improved after treatment for Histoplasma infection. Therefore, this patient's massive purulent pleural effusion was at least partially caused by Histoplasma infection.
4.207031
0.902832
sec[2]/p[0]
en
0.999997
PMC9298875
https://doi.org/10.3389/fpubh.2022.914529
[ "infection", "histoplasma", "pleural", "effusion", "usually", "immune", "associated", "this", "caused", "cases" ]
[ { "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" }, { "code": "1F2A.Z", "title": "Histoplasmosis, unspecified" }, { "code": "1F2A.Y", "title": "Other specified histoplasmosis" }, { "code": "1F2A.1", "title": "Histoplasmosis due to Histoplasma duboisii" }, { "code": "CB2Z", "title": "Pleural, diaphragm or mediastinal disorders, unspecified" }, { "code": "LA76", "title": "Structural developmental anomalies of pleura" } ]
=== ICD-11 CODES FOUND === [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] [1F2A.Z] Histoplasmosis, unspecified Also known as: Histoplasmosis, unspecified | Histoplasmosis | histoplasma infection | reticuloendothelial cytomycosis | cytomycosis [1F2A.Y] Other specified histoplasmosis Also known as: Other specified histoplasmosis | Disseminated histoplasmosis capsulati | Disseminated classical histoplasmosis | Extrapulmonary histoplasmosis | generalised histoplasmosis [1F2A.1] Histoplasmosis due to Histoplasma duboisii Definition: This form of histoplasmosis is endemic to Sub-Saharan Africa and is generally less virulent than histoplasmosis due to H. capsulatum, the classical form which occurs predominantly in tropical and subtropical regions of the Americas but is also seen in Africa and Asia. Otherwise known as African histoplasmosis, histoplasmosis due to Histoplasma duboisii usually involves the skin and subcutaneous tissue, lymph nodes and bones and rarely the lungs and other internal organs. Also known as: Histoplasmosis due to Histoplasma duboisii | African histoplasmosis | Histoplasmosis duboisii [CB2Z] Pleural, diaphragm or mediastinal disorders, unspecified Also known as: Pleural, diaphragm or mediastinal disorders, unspecified [LA76] Structural developmental anomalies of pleura Definition: Anomalies of the lining of the lung (visceral pleura) and thoracic cavity (parietal pleura) Also known as: Structural developmental anomalies of pleura | Malformations of pleura | anomaly of pleura | abnormal pleura | pleural anomaly === GRAPH WALKS === --- Walk 1 --- [1H0Z] Infection, unspecified --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.... --EXCLUDES--> [?] Infection arising from device, implant or graft, not elsewhere classified --- Walk 2 --- [1H0Z] Infection, unspecified --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.... --CHILD--> [?] Predominantly sexually transmitted infections --- Walk 3 --- [1G40] Sepsis without septic shock Def: Sepsis is defined as a life-threatening organ dysfunction caused by a dysregulated host response to infection.... --EXCLUDES--> [?] Sepsis of fetus or newborn --CHILD--> [?] Sepsis of fetus or newborn due to streptococcus, group B --- Walk 4 --- [1G40] Sepsis without septic shock Def: Sepsis is defined as a life-threatening organ dysfunction caused by a dysregulated host response to infection.... --EXCLUDES--> [?] Septicaemia --EXCLUDES--> [?] Sepsis without septic shock Def: Sepsis is defined as a life-threatening organ dysfunction caused by a dysregulated host response to infection.... --- Walk 5 --- [FA10.Z] Direct infections of joint, unspecified --PARENT--> [FA10] Direct infections of joint Def: Hematogenic or non-hematogenic infections of joints.... --CHILD--> [FA10.1] Viral 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.... --CHILD--> [FA10.1] Viral infection of joint
[ "[1H0Z] Infection, unspecified\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....\n --EXCLUDES--> [?] Infection arising from device, implant or graft, not elsewhere classified", "[1H0Z] Infection, unspecified\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....\n --CHILD--> [?] Predominantly sexually transmitted infections", "[1G40] Sepsis without septic shock\n Def: Sepsis is defined as a life-threatening organ dysfunction caused by a dysregulated host response to infection....\n --EXCLUDES--> [?] Sepsis of fetus or newborn\n --CHILD--> [?] Sepsis of fetus or newborn due to streptococcus, group B", "[1G40] Sepsis without septic shock\n Def: Sepsis is defined as a life-threatening organ dysfunction caused by a dysregulated host response to infection....\n --EXCLUDES--> [?] Septicaemia\n --EXCLUDES--> [?] Sepsis without septic shock\n Def: Sepsis is defined as a life-threatening organ dysfunction caused by a dysregulated host response to infection....", "[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--> [FA10.1] Viral 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 --CHILD--> [FA10.1] Viral infection of joint" ]
1H0Z
Infection, unspecified
[ { "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" }, { "from_icd11": "1H0Z", "icd10_code": "I", "icd10_title": "" }, { "from_icd11": "1H0Z", "icd10_code": "B90-B94", "icd10_title": "" }, { "from_icd11": "1H0Z", "icd10_code": "B94", "icd10_title": "Sequelae of other and unspecified infectious and parasitic diseases" } ]
B999
Unspecified infectious disease
The female patient, FL2, was 6 years older than the male patient. At the age of 38, she was diagnosed with uterine myoma and developed multiple primary lung cancer at the age of 60 with no history of smoking. Three primary tumors were located in the right lobe. The loci, diameters, and histology of these lesions were as follows: RS1, 4 cm, invasive adenocarcinoma; RS4, 1 cm, minimally invasive adenocarcinoma; and RS6, 1 cm, adenocarcinoma in situ. These lesions were surgically resected. This patient subsequently developed multiple primary lung cancer in the left lobe and breast cancer at the age of 71. The loci, diameters, and histology of the lung tumors were as follows: LS8, 2.5 cm, invasive adenocarcinoma, acinar pattern predominant; LS8, 1.9 cm, invasive adenocarcinoma, papillary pattern predominant; LS8, 2 cm, invasive adenocarcinoma, papillary pattern predominant; and LS10, 1.8 cm, invasive adenocarcinoma, papillary pattern predominant. The lung and breast tumors were surgically resected. The lung cancer EGFR mutation status was L858R and wild type, probably because of heterogeneity among tumor nodules. Histological and molecular analysis of the breast cancer revealed it to be an invasive ductal carcinoma with a predominant ductal component, estrogen receptor–negative, progesterone receptor–negative, and HeR2-positive. Micrographic views of both patients’ lung cancers are shown in Figure 2 .
3.986328
0.966797
sec[1]/sec[0]/p[1]
en
0.999996
27900359
https://doi.org/10.1101/mcs.a001032
[ "invasive", "adenocarcinoma", "lung", "cancer", "predominant", "pattern", "tumors", "breast", "papillary", "multiple" ]
[ { "code": "5A03.Y", "title": "Other specified thyroiditis" }, { "code": "2C61", "title": "Invasive carcinoma of breast" }, { "code": "2F76&XA90F8", "title": "Invasive mole" }, { "code": "1F20.0Z", "title": "Invasive aspergillosis, unspecified" }, { "code": "2F7C", "title": "Neoplasms of uncertain behaviour of connective or other soft tissue" }, { "code": "2D40", "title": "Adenocarcinoma of unspecified site" }, { "code": "2C0Y", "title": "Other specified malignant neoplasms of intestine" }, { "code": "2C25.0", "title": "Adenocarcinoma of bronchus or lung" }, { "code": "2C94.0", "title": "Adenocarcinoma of urinary bladder" }, { "code": "2B70.0Z", "title": "Adenocarcinoma of oesophagus, unspecified" } ]
=== ICD-11 CODES FOUND === [5A03.Y] Other specified thyroiditis Also known as: Other specified thyroiditis | Riedel thyroiditis | Chronic invasive fibrous thyroiditis | Ligneous thyroiditis | Riedel struma [2C61] Invasive carcinoma of breast Also known as: Invasive carcinoma of breast [1F20.0Z] Invasive aspergillosis, unspecified Also known as: Invasive aspergillosis, unspecified | Invasive aspergillosis | invasive aspergillosis NOS [2F7C] Neoplasms of uncertain behaviour of connective or other soft tissue Also known as: Neoplasms of uncertain behaviour of connective or other soft tissue | Neck hemangiopericytoma | Abdominal desmoid of uncertain behaviour of unspecified site | Abdominal fibromatosis of unspecified site | Aggressive fibromatosis of unspecified site [2D40] Adenocarcinoma of unspecified site Definition: A common cancer characterised by the presence of malignant glandular cells. Morphologically, adenocarcinomas are classified according to the growth pattern (e.g., papillary, alveolar) or according to the secreting product (e.g., mucinous, serous). Representative examples of adenocarcinoma are ductal and lobular breast carcinoma, lung adenocarcinoma, renal cell carcinoma, hepatocellular carcinoma (hepatoma), colon adenocarcinoma, and prostate adenocarcinoma. Also known as: Adenocarcinoma of unspecified site | adenoacanthoma of unspecified site | adenocarcinoid of unspecified site | adenocarcinoid tumour of unspecified site | adenocarcinoma and carcinoid combined of unspecified site [2C0Y] Other specified malignant neoplasms of intestine Also known as: Other specified malignant neoplasms of intestine | Adenocarcinoma of intestine | adenocarcinoma of intestine NOS [2C25.0] Adenocarcinoma of bronchus or lung Definition: A carcinoma that arises from the lung and is characterised by the presence of malignant glandular epithelial cells. There is a male predilection with a male to female ratio of 2:1. Usually lung adenocarcinoma is asymptomatic and is identified through screening studies or as an incidental radiologic finding. If clinical symptoms are present they include shortness of breath, cough, hemoptysis, chest pain, and fever. Tobacco smoke is a known risk factor. Also known as: Adenocarcinoma of bronchus or lung | primary lung adenocarcinoma | lung adenocarcinoma | bronchiolar adenocarcinoma of unspecified site | Mucinous adenocarcinoma of lung [2C94.0] Adenocarcinoma of urinary bladder Definition: A rare adenocarcinoma arising from metaplastic bladder epithelium. It is frequently associated with long-standing local irritation. The majority of cases originate from the trigone and the posterior wall of the bladder. Also known as: Adenocarcinoma of urinary bladder | Adenocarcinoma of bladder [2B70.0Z] Adenocarcinoma of oesophagus, unspecified Also known as: Adenocarcinoma of oesophagus, unspecified | Adenocarcinoma of oesophagus | oesophageal adenocarcinoma === GRAPH WALKS === --- Walk 1 --- [5A03.Y] Other specified thyroiditis --PARENT--> [5A03] Thyroiditis Def: Thyroiditis is the inflammation of the thyroid gland. It includes acute and chronic forms of thyroiditis. Thyroiditis is usually caused by autoimmune reaction to the thyroid, resulting in inflammation... --EXCLUDES--> [?] Acquired hypothyroidism Def: Acquired hypothyroidism is a condition where the thyroid gland produces too little or no thyroid hormone, and the condition arises only after birth.... --- Walk 2 --- [5A03.Y] Other specified thyroiditis --PARENT--> [5A03] Thyroiditis Def: Thyroiditis is the inflammation of the thyroid gland. It includes acute and chronic forms of thyroiditis. Thyroiditis is usually caused by autoimmune reaction to the thyroid, resulting in inflammation... --PARENT--> [?] Disorders of the thyroid gland or thyroid hormones system Def: Disorders due to dysfunction of thyroid gland and regulation systems of thyroid hormone actions including dysfunction of the pituitary, hypothalamus, or thyroid hormone receptors.... --- Walk 3 --- [2C61] Invasive carcinoma of breast --CHILD--> [2C61.2] Invasive pleomorphic lobular carcinoma of breast Def: A grade II invasive lobular carcinoma of the breast, characterised by the presence of neoplastic cells with large and atypical nuclei.... --PARENT--> [2C61] Invasive carcinoma of breast --- Walk 4 --- [2C61] Invasive carcinoma of breast --CHILD--> [2C61.1] Invasive lobular carcinoma of breast Def: An infiltrating lobular adenocarcinoma. The malignant cells lack cohesion and are arranged individually or in a linear manner (Indian files), or as narrow trabeculae within the stroma. The malignant c... --PARENT--> [2C61] Invasive carcinoma of breast --- Walk 5 --- [1F20.0Z] Invasive aspergillosis, unspecified --PARENT--> [1F20.0] Invasive aspergillosis Def: A disease caused by an infection with the fungi Aspergillus. This disease is characterised by colonization and invasion of tissue by Aspergillus in one part of the body and may spread to other parts o... --CHILD--> [1F20.02] Disseminated aspergillosis Def: Invasive aspergillosis affecting three or more organs.... --- Walk 6 --- [1F20.0Z] Invasive aspergillosis, unspecified --PARENT--> [1F20.0] Invasive aspergillosis Def: A disease caused by an infection with the fungi Aspergillus. This disease is characterised by colonization and invasion of tissue by Aspergillus in one part of the body and may spread to other parts o... --CHILD--> [1F20.01] Invasive cerebral aspergillosis
[ "[5A03.Y] Other specified thyroiditis\n --PARENT--> [5A03] Thyroiditis\n Def: Thyroiditis is the inflammation of the thyroid gland. It includes acute and chronic forms of thyroiditis. Thyroiditis is usually caused by autoimmune reaction to the thyroid, resulting in inflammation...\n --EXCLUDES--> [?] Acquired hypothyroidism\n Def: Acquired hypothyroidism is a condition where the thyroid gland produces too little or no thyroid hormone, and the condition arises only after birth....", "[5A03.Y] Other specified thyroiditis\n --PARENT--> [5A03] Thyroiditis\n Def: Thyroiditis is the inflammation of the thyroid gland. It includes acute and chronic forms of thyroiditis. Thyroiditis is usually caused by autoimmune reaction to the thyroid, resulting in inflammation...\n --PARENT--> [?] Disorders of the thyroid gland or thyroid hormones system\n Def: Disorders due to dysfunction of thyroid gland and regulation systems of thyroid hormone actions including dysfunction of the pituitary, hypothalamus, or thyroid hormone receptors....", "[2C61] Invasive carcinoma of breast\n --CHILD--> [2C61.2] Invasive pleomorphic lobular carcinoma of breast\n Def: A grade II invasive lobular carcinoma of the breast, characterised by the presence of neoplastic cells with large and atypical nuclei....\n --PARENT--> [2C61] Invasive carcinoma of breast", "[2C61] Invasive carcinoma of breast\n --CHILD--> [2C61.1] Invasive lobular carcinoma of breast\n Def: An infiltrating lobular adenocarcinoma. The malignant cells lack cohesion and are arranged individually or in a linear manner (Indian files), or as narrow trabeculae within the stroma. The malignant c...\n --PARENT--> [2C61] Invasive carcinoma of breast", "[1F20.0Z] Invasive aspergillosis, unspecified\n --PARENT--> [1F20.0] Invasive aspergillosis\n Def: A disease caused by an infection with the fungi Aspergillus. This disease is characterised by colonization and invasion of tissue by Aspergillus in one part of the body and may spread to other parts o...\n --CHILD--> [1F20.02] Disseminated aspergillosis\n Def: Invasive aspergillosis affecting three or more organs....", "[1F20.0Z] Invasive aspergillosis, unspecified\n --PARENT--> [1F20.0] Invasive aspergillosis\n Def: A disease caused by an infection with the fungi Aspergillus. This disease is characterised by colonization and invasion of tissue by Aspergillus in one part of the body and may spread to other parts o...\n --CHILD--> [1F20.01] Invasive cerebral aspergillosis" ]
5A03.Y
Other specified thyroiditis
[ { "from_icd11": "2F76&XA90F8", "icd10_code": "D392", "icd10_title": "Neoplasm of uncertain behavior of placenta" }, { "from_icd11": "2F7C", "icd10_code": "D481", "icd10_title": "Neoplasm of uncertain behavior of connective and other soft tissue" } ]
D392
Neoplasm of uncertain behavior of placenta
Abdominal TB is defined as TB infection involving the gastrointestinal tract, peritoneum, mesentery, abdominal lymph nodes, and solid visceral organs such as liver, pancreas and spleen . It is sixth most common type of extrapulmonary TB, affecting primarily young adults . It is relatively rare in children . While the ileocecal junction is the most common site reported for abdominal TB , the peritoneum and lymph nodes are the most common sites involved in children with abdominal TB . Mycobacterium tuberculosis and bovis (transmitted through unpasteurized dairy products) are the main pathogens involved. The diagnosis is often delayed because of its non-specific and protean clinical presentation . It is a condition that mimics a variety of inflammatory, infectious and neoplastic gastrointestinal diseases . Fever, abdominal pain and weight loss are the most common symptoms found in children with abdominal TB . There are three patterns of clinical presentation depending on the predominant symptoms: intestinal (colicky abdominal pain, vomiting and gaseous abdominal distension), peritoneal (abdominal distension and ascites) and asymptomatic . Our patient was virtually asymptomatic and had no apparent radiological features of pulmonary TB nor clinical evidences of abdominal TB, other than the urachal discharge. The diagnosis was established during laparoscopy performed for excision of the urachal remnant.
4.105469
0.772949
sec[2]/p[0]
en
0.999998
26850778
https://doi.org/10.1186/s12879-016-1405-6
[ "abdominal", "common", "children", "gastrointestinal", "peritoneum", "lymph", "nodes", "involved", "pain", "distension" ]
[ { "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": "LA89.Z", "title": "Functionally univentricular heart, unspecified" }, { "code": "1E80.Z", "title": "Common warts, unspecified" }, { "code": "LA85.4Z", "title": "Common arterial trunk, unspecified" }, { "code": "ED70.0", "title": "Male pattern hair loss" }, { "code": "DC10.02", "title": "Obstruction of bile duct" } ]
=== 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 [LA89.Z] Functionally univentricular heart, unspecified Also known as: Functionally univentricular heart, unspecified | Functionally univentricular heart | Univentricular cardiopathy | Single ventricle | univentricular heart [1E80.Z] Common warts, unspecified Also known as: Common warts, unspecified | Common warts | verruca vulgaris | viral warts NOS | common warts NOS [LA85.4Z] Common arterial trunk, unspecified Also known as: Common arterial trunk, unspecified | Common arterial trunk | persistent truncus arteriosus | common truncus | common truncus arteriosus [ED70.0] Male pattern hair loss Definition: Male pattern hair loss (common baldness; male androgenetic alopecia) is the result of a progressive, patterned hair loss mediated by exposure to androgens. Although over 90% of men demonstrate some degree of frontoparietal recession of the hairline by the age of 20, the extent of hair loss is genetically determined and only 30% of men ever develop extensive hair loss. Also known as: Male pattern hair loss | Common balding | Male pattern balding | Balding - male pattern | male androgenetic alopecia Includes: Common balding [DC10.02] Obstruction of bile duct Also known as: Obstruction of bile duct | extrahepatic biliary obstruction | extrahepatic bile duct obstruction | bile duct obstruction | bile stasis Excludes: with cholelithiasis === GRAPH WALKS === --- Walk 1 --- [MD81.3] Acute abdomen Def: A clinical syndrome with acute abdominal pain that is severe, and rapid onset. Acute abdomen may be caused by a variety of disorders, injuries, or diseases... --PARENT--> [MD81] Abdominal or pelvic pain Def: Pain, an unpleasant distress sensation occurring in varying degrees of severity, received by nerve ending in the abdominal and pelvic region.... --EXCLUDES--> [?] Flatulence and related conditions Def: Production or presence of gas in the gastrointestinal tract which may be expelled through the anus and other conditions associated with the production or presence of gas in the GI tract.... --- Walk 2 --- [MD81.3] Acute abdomen Def: A clinical syndrome with acute abdominal pain that is severe, and rapid onset. Acute abdomen may be caused by a variety of disorders, injuries, or diseases... --PARENT--> [MD81] Abdominal or pelvic pain Def: Pain, an unpleasant distress sensation occurring in varying degrees of severity, received by nerve ending in the abdominal and pelvic region.... --CHILD--> [MD81.0] Abdominal tenderness --- Walk 3 --- [JA01.0] Abdominal pregnancy Def: A condition characterised by implantation of the embryo within the peritoneal cavity during pregnancy.... --PARENT--> [JA01] Ectopic pregnancy Def: Any condition characterised by implantation of the embryo outside the endometrium and endometrial cavity during pregnancy.... --CHILD--> [JA01.0] Abdominal pregnancy Def: A condition characterised by implantation of the embryo within the peritoneal cavity during pregnancy.... --- 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--> [ME04.0] Fluid in peritoneal cavity
[ "[MD81.3] Acute abdomen\n Def: A clinical syndrome with acute abdominal pain that is severe, and rapid onset. Acute abdomen may be caused by a variety of disorders, injuries, or diseases...\n --PARENT--> [MD81] Abdominal or pelvic pain\n Def: Pain, an unpleasant distress sensation occurring in varying degrees of severity, received by nerve ending in the abdominal and pelvic region....\n --EXCLUDES--> [?] Flatulence and related conditions\n Def: Production or presence of gas in the gastrointestinal tract which may be expelled through the anus and other conditions associated with the production or presence of gas in the GI tract....", "[MD81.3] Acute abdomen\n Def: A clinical syndrome with acute abdominal pain that is severe, and rapid onset. Acute abdomen may be caused by a variety of disorders, injuries, or diseases...\n --PARENT--> [MD81] Abdominal or pelvic pain\n Def: Pain, an unpleasant distress sensation occurring in varying degrees of severity, received by nerve ending in the abdominal and pelvic region....\n --CHILD--> [MD81.0] Abdominal tenderness", "[JA01.0] Abdominal pregnancy\n Def: A condition characterised by implantation of the embryo within the peritoneal cavity during pregnancy....\n --PARENT--> [JA01] Ectopic pregnancy\n Def: Any condition characterised by implantation of the embryo outside the endometrium and endometrial cavity during pregnancy....\n --CHILD--> [JA01.0] Abdominal pregnancy\n Def: A condition characterised by implantation of the embryo within the peritoneal cavity during pregnancy....", "[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--> [ME04.0] Fluid in peritoneal cavity" ]
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": "LA89.Z", "icd10_code": "Q209", "icd10_title": "Congenital malformation of cardiac chambers and connections, unspecified" }, { "from_icd11": "LA85.4Z", "icd10_code": "Q200", "icd10_title": "Common arterial trunk" }, { "from_icd11": "ED70.0", "icd10_code": "L658", "icd10_title": "Other specified nonscarring hair loss" }, { "from_icd11": "DC10.02", "icd10_code": "K831", "icd10_title": "Obstruction of bile duct" } ]
R100
Acute abdomen
Her vital signs were as follows: blood pressure of 104/66 mmHg and 90/61 mmHg in her right and left arms, respectively; heart rate, 96 beats/min; respiratory rate, 16 breaths/min; and temperature, 36.8℃. On physical examination, she had bilateral carotid bruits and mild linear pulsatile tenderness on her left anterior neck along the carotid artery. Additionally, the left radial artery had a weak pulse with radio-radial delay. No right neck tenderness, thyroid tenderness, or lymphadenopathy was noted. The extremities were warm in all four limbs, and no supraclavicular or infraclavicular bruit was noted. Upon eliciting a further history, she complained of exertional pain on her left arm, especially while she was showering her hair using her left hand or typing on the keyboard at work. She had been on sick leave for a week before her presentation due to her neck pain and exertional pain in her left arm. A complete blood count revealed a low haemoglobin level at 9.4 mg/dL (normal range: 13.7-16.8 g/dL) and a high platelet count at 448 × 10 3 /μL (normal range: 158-348 × 10 3 /μL). There was no leucocytosis. The basic metabolic panel was unremarkable. Additional laboratory tests revealed an elevated erythrocyte sedimentation rate (ESR) at 66 mm/h (normal range: 3-15 mm/h) and C-reactive protein (CRP) level at 13.3 mg/dL (normal range: 0-0.14 mg/dL). Thyroid-stimulating hormone was within normal limits.
3.808594
0.980469
sec[1]/p[1]
en
0.999998
PMC9400458
https://doi.org/10.7759/cureus.27227
[ "range", "tenderness", "neck", "pain", "blood", "mmhg", "carotid", "artery", "radial", "thyroid" ]
[ { "code": "QA00.6Y", "title": "Other specified examination of eyes or vision" }, { "code": "4B00.0Z", "title": "Neutropaenia, unspecified" }, { "code": "3B63.1Z", "title": "Acquired thrombocytosis, unspecified" }, { "code": "MA14.1C", "title": "Raised antibody titre" }, { "code": "BD11.1", "title": "Left ventricular failure with mid range ejection fraction" }, { "code": "MD81.0", "title": "Abdominal tenderness" }, { "code": "MD80.Y", "title": "Other specified symptoms or signs of the orofacial complex" }, { "code": "DA0E.7", "title": "Dentofacial parafunctional disorders" }, { "code": "ME65.2", "title": "Pain or tenderness of skin" }, { "code": "8A81.2", "title": "Chronic tension-type headache" } ]
=== ICD-11 CODES FOUND === [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 [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 [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 [MD81.0] Abdominal tenderness Also known as: Abdominal tenderness [MD80.Y] Other specified symptoms or signs of the orofacial complex Also known as: Other specified symptoms or signs of the orofacial complex | Bleeding gums | gum haemorrhage | gingival haemorrhage | gingiva haemorrhage [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 [ME65.2] Pain or tenderness of skin Also known as: Pain or tenderness of skin | Hyperpathia Excludes: Chronic pain [8A81.2] Chronic tension-type headache Definition: A disorder evolving from frequent episodic tension-type headache, with daily or very frequent episodes of headache, typically bilateral, pressing or tightening in quality and of mild to moderate intensity, lasting hours to days, or unremitting. The pain does not worsen with routine physical activity, but may be associated with mild nausea, photophobia or phonophobia. Also known as: Chronic tension-type headache | Chronic tension-type headache associated with pericranial tenderness | Chronic tension-type headache not associated with pericranial tenderness === GRAPH WALKS === --- Walk 1 --- [QA00.6Y] Other specified examination of eyes or vision --PARENT--> [QA00.6] Examination of eyes or vision --EXCLUDES--> [?] Examination for driving license --- Walk 2 --- [QA00.6Y] Other specified examination of eyes or vision --PARENT--> [QA00.6] Examination of eyes or vision --EXCLUDES--> [?] Examination for driving license --- Walk 3 --- [4B00.0Z] Neutropaenia, unspecified --PARENT--> [4B00.0] Neutropenia --RELATED_TO--> [?] Transient neonatal neutropaenia Def: Neonatal neutropaenia can be due to underproduction of the marrow (e.g. hypoxemia due to placental insufficiency, congenital viral disease) or excessive utilization of white blood cells (bacterial sep... --- Walk 4 --- [4B00.0Z] Neutropaenia, unspecified --PARENT--> [4B00.0] Neutropenia --RELATED_TO--> [?] Transient neonatal neutropaenia Def: Neonatal neutropaenia can be due to underproduction of the marrow (e.g. hypoxemia due to placental insufficiency, congenital viral disease) or excessive utilization of white blood cells (bacterial sep... --- Walk 5 --- [3B63.1Z] Acquired thrombocytosis, unspecified --PARENT--> [3B63.1] Acquired thrombocytosis Def: A chronic myeloproliferative neoplasm that involves primarily the megakaryocytic lineage. It is characterised by sustained thrombocytosis in the blood, increased numbers of large, mature megakaryocyte... --CHILD--> [3B63.10] Secondary thrombocytosis --- Walk 6 --- [3B63.1Z] Acquired thrombocytosis, unspecified --PARENT--> [3B63.1] Acquired thrombocytosis Def: A chronic myeloproliferative neoplasm that involves primarily the megakaryocytic lineage. It is characterised by sustained thrombocytosis in the blood, increased numbers of large, mature megakaryocyte... --CHILD--> [3B63.10] Secondary thrombocytosis
[ "[QA00.6Y] Other specified examination of eyes or vision\n --PARENT--> [QA00.6] Examination of eyes or vision\n --EXCLUDES--> [?] Examination for driving license", "[QA00.6Y] Other specified examination of eyes or vision\n --PARENT--> [QA00.6] Examination of eyes or vision\n --EXCLUDES--> [?] Examination for driving license", "[4B00.0Z] Neutropaenia, unspecified\n --PARENT--> [4B00.0] Neutropenia\n --RELATED_TO--> [?] Transient neonatal neutropaenia\n Def: Neonatal neutropaenia can be due to underproduction of the marrow (e.g. hypoxemia due to placental insufficiency, congenital viral disease) or excessive utilization of white blood cells (bacterial sep...", "[4B00.0Z] Neutropaenia, unspecified\n --PARENT--> [4B00.0] Neutropenia\n --RELATED_TO--> [?] Transient neonatal neutropaenia\n Def: Neonatal neutropaenia can be due to underproduction of the marrow (e.g. hypoxemia due to placental insufficiency, congenital viral disease) or excessive utilization of white blood cells (bacterial sep...", "[3B63.1Z] Acquired thrombocytosis, unspecified\n --PARENT--> [3B63.1] Acquired thrombocytosis\n Def: A chronic myeloproliferative neoplasm that involves primarily the megakaryocytic lineage. It is characterised by sustained thrombocytosis in the blood, increased numbers of large, mature megakaryocyte...\n --CHILD--> [3B63.10] Secondary thrombocytosis", "[3B63.1Z] Acquired thrombocytosis, unspecified\n --PARENT--> [3B63.1] Acquired thrombocytosis\n Def: A chronic myeloproliferative neoplasm that involves primarily the megakaryocytic lineage. It is characterised by sustained thrombocytosis in the blood, increased numbers of large, mature megakaryocyte...\n --CHILD--> [3B63.10] Secondary thrombocytosis" ]
QA00.6Y
Other specified examination of eyes or vision
[ { "from_icd11": "3B63.1Z", "icd10_code": "D473", "icd10_title": "Essential (hemorrhagic) thrombocythemia" }, { "from_icd11": "MA14.1C", "icd10_code": "R760", "icd10_title": "Raised antibody titer" } ]
D473
Essential (hemorrhagic) thrombocythemia
A 66-year-old woman presented with an incidental finding of a lung mass (not otherwise specified), accompanied by palpable masses in the hands, legs, and back. She had a history of surgery for schwannoma in 1998. Further history-taking revealed that this was a spinal schwannoma. She had experienced severe back pain prior to surgery. In 2007, painless neurogenic tumors were incidentally found in the upper and lower portion of the psoas muscle: an ovoid-shaped epidural mass measuring 3.7 cm, in the lower neck, and at the level of the third and fourth cervical vertebrae. No further surgery was performed. In 2013, she underwent excision surgery for incidental neurogenic tumors of the right shoulder and palm. The diagnosis of cellular schwannoma was confirmed via excisional biopsy. These were accompanied by multiple masses with cystic degeneration at the level of the seventh cervical vertebra and first thoracic vertebra. Both show a connection to the neural foramen. In 2014, she underwent an additional surgery for a palpable infraclavicular mass, which was later confirmed as an ancient schwannoma. Additional masses were found in the brachial plexus and right median nerve . With regard to family history, the proband had four children. Only her second daughter was diagnosed with a schwannoma. Other children have been reported to have no schwannoma. The details of the daughters are stated in Section 2.2 .
3.845703
0.983887
sec[1]/sec[0]/p[0]
en
0.999997
36363549
https://doi.org/10.3390/medicina58111592
[ "schwannoma", "masses", "incidental", "accompanied", "palpable", "back", "neurogenic", "tumors", "cervical", "vertebra" ]
[ { "code": "2F3Y", "title": "Benign neoplasms except of mesenchymal origin, of other specified site" }, { "code": "2F24", "title": "Benign cutaneous neoplasms of neural or nerve sheath origin" }, { "code": "2A02.3", "title": "Benign neoplasm of cranial nerves" }, { "code": "2F30.Y", "title": "Other specified benign neoplasm of breast" }, { "code": "LD2D.11", "title": "Neurofibromatosis type 2" }, { "code": "MD82", "title": "Intra-abdominal or pelvic swelling, mass or lump" }, { "code": "ME61", "title": "Subcutaneous swelling, mass or lump of uncertain or unspecified nature" }, { "code": "2F9Z", "title": "Neoplasms of unknown behaviour of unspecified site" }, { "code": "MD41", "title": "Clinical findings on diagnostic imaging of lung" }, { "code": "MG01", "title": "Clinical findings on diagnostic imaging of urinary organs" } ]
=== ICD-11 CODES FOUND === [2F3Y] Benign neoplasms except of mesenchymal origin, of other specified site Also known as: Benign neoplasms except of mesenchymal origin, of other specified site | Benign neoplasm of lymph vessels | Benign neoplasm of lymph nodes | Benign neoplasm of peripheral nerves or autonomic nervous system | benign neoplasm of the nerve NOS [2F24] Benign cutaneous neoplasms of neural or nerve sheath origin Also known as: Benign cutaneous neoplasms of neural or nerve sheath origin | Palisaded encapsulated neuroma | Cutaneous neurofibroma | Cutaneous schwannoma | Cutaneous neurolemmoma [2A02.3] Benign neoplasm of cranial nerves Definition: This is a tumour of cranial nerves having none of the characteristics of a malignant neoplasm. Also known as: Benign neoplasm of cranial nerves | neurinoma of unspecified site | Vestibular schwannoma | acoustic schwannoma | Benign neoplasm of abducens nerve Includes: Vestibular schwannoma [2F30.Y] Other specified benign neoplasm of breast Also known as: Other specified benign neoplasm of breast | Benign cystosarcoma phyllodes | Breast apocrine adenoma | Serocystic disease of Brodie | Pleomorphic adenoma of breast [LD2D.11] Neurofibromatosis type 2 Definition: Neurofibromatosis type 2 (NF2) is a tumour-prone disorder characterised by the development of multiple schwannomas and meningiomas. Also known as: Neurofibromatosis type 2 | Familial acoustic neuroma | Familial vestibular schwannoma | Neurofibromatosis, central type | Bilateral acoustic neurofibromatosis [MD82] Intra-abdominal or pelvic swelling, mass or lump Definition: This refers to the presence of abdominal or pelvic wall swelling, mass or tumour in the abdominal and pelvic regions. These mass or tumours can be recognised by visual examination and/or palpation. Also known as: Intra-abdominal or pelvic swelling, mass or lump | Abdominal mass without further specification | mass in abdomen | intra-abdominal lump | intra-abdominal mass Excludes: Abdominal distension | Ascites [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 [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 [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 [MG01] Clinical findings on diagnostic imaging of urinary organs Also known as: Clinical findings on diagnostic imaging of urinary organs | abnormal diagnostic imaging of urinary organs | Bladder filling defect | Kidney filling defect | Renal mass Excludes: hypertrophy of kidney === GRAPH WALKS === --- Walk 1 --- [2F3Y] Benign neoplasms except of mesenchymal origin, of other specified site --PARENT--> [?] Benign neoplasms except of mesenchymal origin --CHILD--> [2E90] Benign neoplasm of lip, oral cavity or pharynx --- Walk 2 --- [2F3Y] Benign neoplasms except of mesenchymal origin, of other specified site --PARENT--> [?] Benign neoplasms except of mesenchymal origin --CHILD--> [2E92] Benign neoplasm of digestive organs Def: A neoplasm of the digestive system which is characterised by the absence of morphologic features associated with malignancy (severe cytologic atypia, tumour cell necrosis, and high mitotic rate). Beni... --- Walk 3 --- [2F24] Benign cutaneous neoplasms of neural or nerve sheath origin --PARENT--> [?] Benign cutaneous neoplasms Def: Abnormal growth of the cells that comprise the tissues of the skin, without any evidence of malignancy.... --CHILD--> [2F20] Benign cutaneous melanocytic neoplasms --- Walk 4 --- [2F24] Benign cutaneous neoplasms of neural or nerve sheath origin --PARENT--> [?] Benign cutaneous neoplasms Def: Abnormal growth of the cells that comprise the tissues of the skin, without any evidence of malignancy.... --CHILD--> [2F20] Benign cutaneous melanocytic neoplasms --- Walk 5 --- [2A02.3] Benign neoplasm of cranial nerves Def: This is a tumour of cranial nerves having none of the characteristics of a malignant neoplasm.... --PARENT--> [2A02] Primary neoplasm of spinal cord, cranial nerves, paraspinal nerves or remaining parts of central nervous system --CHILD--> [2A02.2] Primary neoplasm of spinal cord of unknown or unspecified type --- Walk 6 --- [2A02.3] Benign neoplasm of cranial nerves Def: This is a tumour of cranial nerves having none of the characteristics of a malignant neoplasm.... --PARENT--> [2A02] Primary neoplasm of spinal cord, cranial nerves, paraspinal nerves or remaining parts of central nervous system --PARENT--> [?] Neoplasms of central nervous system or related structures Def: A benign or malignant neoplasm that affects the brain, meninges, or spinal cord. Representative examples of primary neoplasms include astrocytoma, oligodendroglioma, ependymoma, and meningioma....
[ "[2F3Y] Benign neoplasms except of mesenchymal origin, of other specified site\n --PARENT--> [?] Benign neoplasms except of mesenchymal origin\n --CHILD--> [2E90] Benign neoplasm of lip, oral cavity or pharynx", "[2F3Y] Benign neoplasms except of mesenchymal origin, of other specified site\n --PARENT--> [?] Benign neoplasms except of mesenchymal origin\n --CHILD--> [2E92] Benign neoplasm of digestive organs\n Def: A neoplasm of the digestive system which is characterised by the absence of morphologic features associated with malignancy (severe cytologic atypia, tumour cell necrosis, and high mitotic rate). Beni...", "[2F24] Benign cutaneous neoplasms of neural or nerve sheath origin\n --PARENT--> [?] Benign cutaneous neoplasms\n Def: Abnormal growth of the cells that comprise the tissues of the skin, without any evidence of malignancy....\n --CHILD--> [2F20] Benign cutaneous melanocytic neoplasms", "[2F24] Benign cutaneous neoplasms of neural or nerve sheath origin\n --PARENT--> [?] Benign cutaneous neoplasms\n Def: Abnormal growth of the cells that comprise the tissues of the skin, without any evidence of malignancy....\n --CHILD--> [2F20] Benign cutaneous melanocytic neoplasms", "[2A02.3] Benign neoplasm of cranial nerves\n Def: This is a tumour of cranial nerves having none of the characteristics of a malignant neoplasm....\n --PARENT--> [2A02] Primary neoplasm of spinal cord, cranial nerves, paraspinal nerves or remaining parts of central nervous system\n --CHILD--> [2A02.2] Primary neoplasm of spinal cord of unknown or unspecified type", "[2A02.3] Benign neoplasm of cranial nerves\n Def: This is a tumour of cranial nerves having none of the characteristics of a malignant neoplasm....\n --PARENT--> [2A02] Primary neoplasm of spinal cord, cranial nerves, paraspinal nerves or remaining parts of central nervous system\n --PARENT--> [?] Neoplasms of central nervous system or related structures\n Def: A benign or malignant neoplasm that affects the brain, meninges, or spinal cord. Representative examples of primary neoplasms include astrocytoma, oligodendroglioma, ependymoma, and meningioma...." ]
2F3Y
Benign neoplasms except of mesenchymal origin, of other specified site
[ { "from_icd11": "2A02.3", "icd10_code": "D333", "icd10_title": "Benign neoplasm of cranial nerves" }, { "from_icd11": "MD82", "icd10_code": "R1900", "icd10_title": "Intra-abdominal and pelvic swelling, mass and lump, unspecified site" }, { "from_icd11": "MD82", "icd10_code": "R1909", "icd10_title": "Other intra-abdominal and pelvic swelling, mass and lump" }, { "from_icd11": "MD82", "icd10_code": "R1902", "icd10_title": "Left upper quadrant abdominal swelling, mass and lump" }, { "from_icd11": "MD82", "icd10_code": "R1904", "icd10_title": "Left lower quadrant abdominal swelling, mass and lump" }, { "from_icd11": "MD82", "icd10_code": "R1903", "icd10_title": "Right lower quadrant abdominal swelling, mass and lump" }, { "from_icd11": "MD82", "icd10_code": "R1901", "icd10_title": "Right upper quadrant abdominal swelling, mass and lump" }, { "from_icd11": "MD82", "icd10_code": "R1907", "icd10_title": "Generalized intra-abdominal and pelvic swelling, mass and lump" }, { "from_icd11": "MD82", "icd10_code": "R1906", "icd10_title": "Epigastric swelling, mass or lump" }, { "from_icd11": "MD82", "icd10_code": "R190", "icd10_title": "Intra-abdominal and pelvic swelling, mass and lump" }, { "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" } ]
D333
Benign neoplasm of cranial nerves
Pathologic examination of the specimen revealed immature teratoma elements involving the right ovary, omentum, and peritoneal nodules. The ovarian tumor measured 20 cm in greatest dimension and weighed 1704.4 g. The cut section of the bivalved tumor demonstrated an irregular, predominantly solid, sporadically cystic, yellowish mass . Microscopic evaluation demonstrated a preponderance (approximately 80%) of mature elements, including cartilage, bone, skin, respiratory and gastrointestinal epithelium, among others. The remaining 20% of the ovarian tumor, as well as the omental and peritoneal lesions, demonstrated immature neuroepithelial elements, comprised of scattered aggregates of primitive appearing, mitotically active cells forming rosette-like structures . The maximal number of low-power microscopic fields (40x total magnification) showing aggregates of immature neuroepithelium in any one slide of the ovarian tumor was 3, consistent with a grade 2 tumor on a 3-tiered scale and a high-grade tumor on a 2-tiered scale. Fig. 2 Pathologic examination. (A) Macroscopic appearance of the ovarian tumoral cut surface. (B) Low magnification image of an “immature” area of tumor, comprised of abundant immature neuroepithelial elements. (C) High power magnification demonstrated neuroepithelial elements comprised of aggregates of primitive appearing, mitotically active cells forming rosette-like structures.
4.09375
0.570801
sec[2]/p[0]
en
0.999996
PMC9068995
https://doi.org/10.1016/j.gore.2021.100910
[ "tumor", "immature", "elements", "ovarian", "neuroepithelial", "comprised", "aggregates", "magnification", "pathologic", "peritoneal" ]
[ { "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": "KA21.4Z", "title": "Preterm newborn, unspecified" }, { "code": "KB2B", "title": "Primary atelectasis of newborn" }, { "code": "KA21.3Z", "title": "Extreme prematurity of newborn, unspecified" }, { "code": "LA75.Y", "title": "Other specified structural developmental anomalies of lungs" }, { "code": "9B10.2Y", "title": "Other specified cataracts" } ]
=== 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 [KA21.4Z] Preterm newborn, unspecified Also known as: Preterm newborn, unspecified | Preterm newborn | immaturity | other preterm infants, unspecified | other preterm infants, unspecified weight [KB2B] Primary atelectasis of newborn Definition: Failure of the lungs to expand after birth, as in stillborn infants or in liveborn infants who die before respiration is established Also known as: Primary atelectasis of newborn | Primary failure to expand terminal respiratory units | immature lungs | primary atelectasis | pulmonary immaturity NOS Includes: Primary failure to expand terminal respiratory units [KA21.3Z] Extreme prematurity of newborn, unspecified Also known as: Extreme prematurity of newborn, unspecified | Extreme prematurity of newborn | very premature baby | extreme prematurity | severe prem NOS [LA75.Y] Other specified structural developmental anomalies of lungs Also known as: Other specified structural developmental anomalies of lungs | Anomalies of lung lobation | Lung isomerism | Congenital pulmonary lymphangiectasia | Pulmonary lymphangiomatosis [9B10.2Y] Other specified cataracts Also known as: Other specified cataracts | Cataract in systemic disorders | Cataract in degenerative disorders | Cataract in inflammatory disorders | Tetanic cataract === GRAPH WALKS === --- Walk 1 --- [2F9Z] Neoplasms of unknown behaviour of unspecified site --PARENT--> [?] Neoplasms of unknown behaviour, except of lymphoid, haematopoietic, central nervous system or related tissues --CHILD--> [2F92] Neoplasms of unknown behaviour of skin --- Walk 2 --- [2F9Z] Neoplasms of unknown behaviour of unspecified site --PARENT--> [?] Neoplasms of unknown behaviour, except of lymphoid, haematopoietic, central nervous system or related tissues --CHILD--> [2F92] Neoplasms of unknown behaviour of skin --- Walk 3 --- [ME61] Subcutaneous swelling, mass or lump of uncertain or unspecified nature Def: One or more localised subcutaneous soft tissue masses of undetermined or unspecified nature... --EXCLUDES--> [?] Breast lump or mass female --PARENT--> [?] Symptoms, signs or clinical findings involving the female genital system --- Walk 4 --- [ME61] Subcutaneous swelling, mass or lump of uncertain or unspecified nature Def: One or more localised subcutaneous soft tissue masses of undetermined or unspecified nature... --EXCLUDES--> [?] Breast lump or mass female --PARENT--> [?] Symptoms, signs or clinical findings involving the female genital system --- Walk 5 --- [2E6Z] Carcinoma in situ of unspecified site --PARENT--> [?] In situ neoplasms, except of lymphoid, haematopoietic, central nervous system or related tissues --CHILD--> [2E62] Carcinoma in situ of middle ear or respiratory system --- 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....
[ "[2F9Z] Neoplasms of unknown behaviour of unspecified site\n --PARENT--> [?] Neoplasms of unknown behaviour, except of lymphoid, haematopoietic, central nervous system or related tissues\n --CHILD--> [2F92] Neoplasms of unknown behaviour of skin", "[2F9Z] Neoplasms of unknown behaviour of unspecified site\n --PARENT--> [?] Neoplasms of unknown behaviour, except of lymphoid, haematopoietic, central nervous system or related tissues\n --CHILD--> [2F92] Neoplasms of unknown behaviour of skin", "[ME61] Subcutaneous swelling, mass or lump of uncertain or unspecified nature\n Def: One or more localised subcutaneous soft tissue masses of undetermined or unspecified nature...\n --EXCLUDES--> [?] Breast lump or mass female\n --PARENT--> [?] Symptoms, signs or clinical findings involving the female genital system", "[ME61] Subcutaneous swelling, mass or lump of uncertain or unspecified nature\n Def: One or more localised subcutaneous soft tissue masses of undetermined or unspecified nature...\n --EXCLUDES--> [?] Breast lump or mass female\n --PARENT--> [?] Symptoms, signs or clinical findings involving the female genital system", "[2E6Z] Carcinoma in situ of unspecified site\n --PARENT--> [?] In situ neoplasms, except of lymphoid, haematopoietic, central nervous system or related tissues\n --CHILD--> [2E62] Carcinoma in situ of middle ear or respiratory 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...." ]
2F9Z
Neoplasms of unknown behaviour of unspecified site
[ { "from_icd11": "2F9Z", "icd10_code": "D487", "icd10_title": "Neoplasm of uncertain behavior of other specified sites" }, { "from_icd11": "2F9Z", "icd10_code": "D482", "icd10_title": "Neoplasm of uncertain behavior of peripheral nerves and autonomic nervous system" }, { "from_icd11": "2F9Z", "icd10_code": "D37-D48", "icd10_title": "" }, { "from_icd11": "2F9Z", "icd10_code": "D377", "icd10_title": "" }, { "from_icd11": "2F9Z", "icd10_code": "D48", "icd10_title": "Neoplasm of uncertain behavior of other and unspecified sites" }, { "from_icd11": "2F9Z", "icd10_code": "D489", "icd10_title": "Neoplasm of uncertain behavior, unspecified" }, { "from_icd11": "ME61", "icd10_code": "R2240", "icd10_title": "Localized swelling, mass and lump, unspecified lower limb" }, { "from_icd11": "ME61", "icd10_code": "R2232", "icd10_title": "Localized swelling, mass and lump, left upper limb" }, { "from_icd11": "ME61", "icd10_code": "R2242", "icd10_title": "Localized swelling, mass and lump, left lower limb" }, { "from_icd11": "ME61", "icd10_code": "R2231", "icd10_title": "Localized swelling, mass and lump, right upper limb" }, { "from_icd11": "ME61", "icd10_code": "R2241", "icd10_title": "Localized swelling, mass and lump, right lower limb" }, { "from_icd11": "ME61", "icd10_code": "R2233", "icd10_title": "Localized swelling, mass and lump, upper limb, bilateral" }, { "from_icd11": "ME61", "icd10_code": "R2243", "icd10_title": "Localized swelling, mass and lump, lower limb, bilateral" }, { "from_icd11": "ME61", "icd10_code": "R2230", "icd10_title": "Localized swelling, mass and lump, unspecified upper limb" }, { "from_icd11": "ME61", "icd10_code": "R220", "icd10_title": "Localized swelling, mass and lump, head" } ]
D487
Neoplasm of uncertain behavior of other specified sites
A liver transplant workup was initiated considering his hepatic encephalopathy and coagulopathy. He was started on empirical antibiotics, coagulation correction, and sustained low-efficiency dialysis (SLED). Workup for all infectious causes, both bacterial and viral, was negative except for bio-fire from the nasopharyngeal swab, which was positive for Enterovirus. Both the urine and stool polymerase chain reaction (PCR) for the enterovirus were negative. T2, urine legionella, Streptococcus pneumoniae, Epstein Barr virus (EBV) DNA, hepatitis serology, and (human immunodeficiency virus) HIV were negative. Eventually, the patient required an orthotopic liver transplant within the first 48 hours of presentation with a MELD score of 40. The explant liver pathology revealed microvesicular steatosis and coagulative necrosis. His postoperative course was complicated by persistently elevated CPK and severe ongoing rhabdomyolysis. The patient had to undergo multiple fasciotomies for bilateral lower extremity compartment syndrome. In view of his persistent rhabdomyolysis, he had a muscle biopsy which revealed necrosis without viral inclusion particles. The patient had a lumbar puncture which was negative for infectious etiology. The patient also had an MRI imaging of his brain , in view of his persisting altered sensorium. Imaging revealed multiple small vessel ischemic changes, not correlating with his age.
3.861328
0.979004
sec[1]/p[2]
en
0.999997
PMC9123819
https://doi.org/10.7759/cureus.24336
[ "liver", "which", "transplant", "workup", "infectious", "both", "viral", "enterovirus", "urine", "virus" ]
[ { "code": "DB9Z", "title": "Diseases of liver, unspecified" }, { "code": "DB97.Z", "title": "Inflammatory liver disease, unspecified" }, { "code": "DB99.7", "title": "Hepatic failure without mention whether acute or chronic" }, { "code": "LB20.0Y", "title": "Other specified structural developmental anomalies of liver" }, { "code": "LB20.0Z", "title": "Structural developmental anomalies of liver, unspecified" }, { "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": "QB63.Z", "title": "Presence of transplanted organ or tissue, unspecified" } ]
=== ICD-11 CODES FOUND === [DB9Z] Diseases of liver, unspecified Also known as: Diseases of liver, unspecified | liver disease | liver condition NOS | organ liver disease | hepatopathy [DB97.Z] Inflammatory liver disease, unspecified Also known as: Inflammatory liver disease, unspecified | Certain specified inflammatory liver diseases | Nonspecific reactive hepatitis | inflammatory liver disease | hepatitis NOS [DB99.7] Hepatic failure without mention whether acute or chronic Also known as: Hepatic failure without mention whether acute or chronic | liver decompensation | liver function failure | hepatic failure NOS | liver failure NOS [LB20.0Y] Other specified structural developmental anomalies of liver Also known as: Other specified structural developmental anomalies of liver | Alagille syndrome | Alagille-Watson syndrome | Arteriohepatic dysplasia | Syndromic bile duct paucity [LB20.0Z] Structural developmental anomalies of liver, unspecified Also known as: Structural developmental anomalies of liver, unspecified | Structural developmental anomalies of liver | Malformations of liver | congenital anomaly of liver | congenital malformation of liver [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 [QB63.Z] Presence of transplanted organ or tissue, unspecified Also known as: Presence of transplanted organ or tissue, unspecified | Presence of transplanted organ or tissue | transplanted organ or tissue status | organ or tissue replaced by heterogenous or homogenous transplant | organ transplant === GRAPH WALKS === --- Walk 1 --- [DB9Z] Diseases of liver, unspecified --PARENT--> [?] Diseases of liver --RELATED_TO--> [?] Structural developmental anomalies of liver --- Walk 2 --- [DB9Z] Diseases of liver, unspecified --PARENT--> [?] Diseases of liver --EXCLUDES--> [?] Unspecified jaundice Def: A clinical manifestation of hyperbilirubinemia of unspecified origin, characterised by the yellowish staining of the skin; mucus membranes and sclera.... --- Walk 3 --- [DB97.Z] Inflammatory liver disease, unspecified --PARENT--> [DB97] Certain specified inflammatory liver diseases --CHILD--> [DB97.0] Idiopathic granulomatous hepatitis --- Walk 4 --- [DB97.Z] Inflammatory liver disease, unspecified --PARENT--> [DB97] Certain specified inflammatory liver diseases --EXCLUDES--> [?] Acute viral hepatitis Def: A group of liver diseases characterised by liver inflammation and fibrosis, caused by less than 6 months of infection with one or more of hepatitis B virus, hepatitis C virus and hepatitis D virus, wi... --- Walk 5 --- [DB99.7] Hepatic failure without mention whether acute or chronic --PARENT--> [DB99] 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.... --EXCLUDES--> [?] Drug-induced or toxic liver disease Def: Drug-induced or toxic liver disease is hepatotoxicity as injury to the liver that is associated with impaired liver function caused by exposure to a drug or another noninfectious agent.... --- Walk 6 --- [DB99.7] Hepatic failure without mention whether acute or chronic --PARENT--> [DB99] 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.... --RELATED_TO--> [?] Cirrhotic cardiomyopathy Def: Cirrhotic cardiomyopathy is defined as chronic cardiac dysfunction in patients with cirrhosis characterised by blunted contractile responsiveness to stress/exercise and-or altered diastolic relaxation...
[ "[DB9Z] Diseases of liver, unspecified\n --PARENT--> [?] Diseases of liver\n --RELATED_TO--> [?] Structural developmental anomalies of liver", "[DB9Z] Diseases of liver, unspecified\n --PARENT--> [?] Diseases of liver\n --EXCLUDES--> [?] Unspecified jaundice\n Def: A clinical manifestation of hyperbilirubinemia of unspecified origin, characterised by the yellowish staining of the skin; mucus membranes and sclera....", "[DB97.Z] Inflammatory liver disease, unspecified\n --PARENT--> [DB97] Certain specified inflammatory liver diseases\n --CHILD--> [DB97.0] Idiopathic granulomatous hepatitis", "[DB97.Z] Inflammatory liver disease, unspecified\n --PARENT--> [DB97] Certain specified inflammatory liver diseases\n --EXCLUDES--> [?] Acute viral hepatitis\n Def: A group of liver diseases characterised by liver inflammation and fibrosis, caused by less than 6 months of infection with one or more of hepatitis B virus, hepatitis C virus and hepatitis D virus, wi...", "[DB99.7] Hepatic failure without mention whether acute or chronic\n --PARENT--> [DB99] 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....\n --EXCLUDES--> [?] Drug-induced or toxic liver disease\n Def: Drug-induced or toxic liver disease is hepatotoxicity as injury to the liver that is associated with impaired liver function caused by exposure to a drug or another noninfectious agent....", "[DB99.7] Hepatic failure without mention whether acute or chronic\n --PARENT--> [DB99] 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....\n --RELATED_TO--> [?] Cirrhotic cardiomyopathy\n Def: Cirrhotic cardiomyopathy is defined as chronic cardiac dysfunction in patients with cirrhosis characterised by blunted contractile responsiveness to stress/exercise and-or altered diastolic relaxation..." ]
DB9Z
Diseases of liver, unspecified
[ { "from_icd11": "DB9Z", "icd10_code": "K7681", "icd10_title": "Hepatopulmonary syndrome" }, { "from_icd11": "DB9Z", "icd10_code": "K7689", "icd10_title": "Other specified diseases of liver" }, { "from_icd11": "DB9Z", "icd10_code": "K769", "icd10_title": "Liver disease, unspecified" }, { "from_icd11": "DB9Z", "icd10_code": "K77", "icd10_title": "Liver disorders in diseases classified elsewhere" }, { "from_icd11": "DB9Z", "icd10_code": "K762", "icd10_title": "Central hemorrhagic necrosis of liver" }, { "from_icd11": "DB9Z", "icd10_code": "K70-K77", "icd10_title": "" }, { "from_icd11": "DB9Z", "icd10_code": "K778", "icd10_title": "" }, { "from_icd11": "DB9Z", "icd10_code": "K72", "icd10_title": "Hepatic failure, not elsewhere classified" }, { "from_icd11": "DB9Z", "icd10_code": "K76", "icd10_title": "Other diseases of liver" }, { "from_icd11": "DB9Z", "icd10_code": "K768", "icd10_title": "Other specified diseases of liver" }, { "from_icd11": "DB97.Z", "icd10_code": "K7581", "icd10_title": "Nonalcoholic steatohepatitis (NASH)" }, { "from_icd11": "DB97.Z", "icd10_code": "K7589", "icd10_title": "Other specified inflammatory liver diseases" }, { "from_icd11": "DB97.Z", "icd10_code": "K759", "icd10_title": "Inflammatory liver disease, unspecified" }, { "from_icd11": "DB97.Z", "icd10_code": "K752", "icd10_title": "Nonspecific reactive hepatitis" }, { "from_icd11": "DB97.Z", "icd10_code": "K75", "icd10_title": "Other inflammatory liver diseases" } ]
K7681
Hepatopulmonary syndrome
Hereditary haemorrhagic telangiectasia (HHT) is a rare autosomal dominant disorder characterized by arteriovenous malformations (AVMs) of the internal organs and mucocutaneous telangiectasias ( 1 ). The estimated prevalence is 1/5,000–1/8,000 people ( 2 ). The liver is the most common visceral organ susceptible to HHT, but such cases are usually asymptomatic. More than half of patients with HHT have hepatic vascular malformations (VMs), but only 8% show symptoms ( 3 ). Although asymptomatic liver VMs do not require treatment, symptomatic liver VMs must be treated aggressively since they increase mortality. However, the treatment for liver VMs is limited to anti-angiogenesis, arterial embolization, and ligation and banding of the hepatic artery. Liver transplantation is an effective treatment option, whereas long-term immunosuppressive therapy remains a trade-off of this choice, especially for younger patients. Therefore, more effective treatments for liver VMs should be explored. Here, we report a 30-year-old woman who had HHT with hepatic AVMs and underwent right hemihepatectomy combined with ligation of the common hepatic artery and gastroduodenal artery because of her disease characteristics. Although long-term outcomes require further follow-up, the successful recovery and discharge of the patient demonstrate the feasibility of this procedure for the treatment of partial HHT with hepatic AVMs.
4.210938
0.852539
sec[0]/p[0]
en
0.999997
PMC9395736
https://doi.org/10.3389/fsurg.2022.900297
[ "liver", "hepatic", "avms", "artery", "malformations", "common", "asymptomatic", "patients", "although", "require" ]
[ { "code": "DB9Z", "title": "Diseases of liver, unspecified" }, { "code": "DB97.Z", "title": "Inflammatory liver disease, unspecified" }, { "code": "DB99.7", "title": "Hepatic failure without mention whether acute or chronic" }, { "code": "LB20.0Y", "title": "Other specified structural developmental anomalies of liver" }, { "code": "LB20.0Z", "title": "Structural developmental anomalies of liver, unspecified" }, { "code": "LA90.3Y", "title": "Other specified peripheral arteriovenous malformations" }, { "code": "BD5Z", "title": "Diseases of arteries or arterioles, unspecified" }, { "code": "BD52", "title": "Certain specified disorders of arteries or arterioles" }, { "code": "BD52.3", "title": "Rupture of artery" }, { "code": "BD52.2", "title": "Stricture of artery" } ]
=== ICD-11 CODES FOUND === [DB9Z] Diseases of liver, unspecified Also known as: Diseases of liver, unspecified | liver disease | liver condition NOS | organ liver disease | hepatopathy [DB97.Z] Inflammatory liver disease, unspecified Also known as: Inflammatory liver disease, unspecified | Certain specified inflammatory liver diseases | Nonspecific reactive hepatitis | inflammatory liver disease | hepatitis NOS [DB99.7] Hepatic failure without mention whether acute or chronic Also known as: Hepatic failure without mention whether acute or chronic | liver decompensation | liver function failure | hepatic failure NOS | liver failure NOS [LB20.0Y] Other specified structural developmental anomalies of liver Also known as: Other specified structural developmental anomalies of liver | Alagille syndrome | Alagille-Watson syndrome | Arteriohepatic dysplasia | Syndromic bile duct paucity [LB20.0Z] Structural developmental anomalies of liver, unspecified Also known as: Structural developmental anomalies of liver, unspecified | Structural developmental anomalies of liver | Malformations of liver | congenital anomaly of liver | congenital malformation of liver [LA90.3Y] Other specified peripheral arteriovenous malformations Also known as: Other specified peripheral arteriovenous malformations | Spinal arteriovenous malformation | Foix-Alajouanine syndrome | Cerebrofacial arteriovenous metameric syndrome | CAMS - [Cerebrofacial arteriovenous metameric syndrome] [BD5Z] Diseases of arteries or arterioles, unspecified Also known as: Diseases of arteries or arterioles, unspecified | artery disease NOS | arterial disease NOS | arteriolar disease NOS | disorder of artery NOS [BD52] Certain specified disorders of arteries or arterioles Also known as: Certain specified disorders of arteries or arterioles | Aortic dilatation - joint hypermobility - arterial tortuosity | Generalised arterial calcification of infancy | Median arcuate ligament syndrome | Aortic root abscess Excludes: collagen (vascular) diseases | Hypersensitivity angiitis | Acute arterial occlusion [BD52.3] Rupture of artery Also known as: Rupture of artery | ruptured artery | artery fistula | Aortic duodenal fistula | Aortic colon fistula Excludes: traumatic rupture of artery - see injury of blood vessel by body region [BD52.2] Stricture of artery Also known as: Stricture of artery | arterial stenosis | arterial stricture | artery stricture | stenosis of artery === GRAPH WALKS === --- Walk 1 --- [DB9Z] Diseases of liver, unspecified --PARENT--> [?] Diseases of liver --RELATED_TO--> [?] Structural developmental anomalies of liver --- Walk 2 --- [DB9Z] Diseases of liver, unspecified --PARENT--> [?] Diseases of liver --CHILD--> [DB90] Infectious liver disease --- Walk 3 --- [DB97.Z] Inflammatory liver disease, unspecified --PARENT--> [DB97] Certain specified inflammatory liver diseases --CHILD--> [DB97.2] Chronic hepatitis, not elsewhere classified --- Walk 4 --- [DB97.Z] Inflammatory liver disease, unspecified --PARENT--> [DB97] Certain specified inflammatory liver diseases --RELATED_TO--> [?] Hepatic sarcoidosis Def: This is a syndrome involving abnormal collections of chronic inflammatory cells (granulomas) that can form as nodules in multiple organs, of the liver.... --- Walk 5 --- [DB99.7] Hepatic failure without mention whether acute or chronic --PARENT--> [DB99] 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.... --RELATED_TO--> [?] Liver disorders in pregnancy, childbirth or the puerperium Def: Any disorder affecting females, characterised by pathological changes to the liver that occur during pregnancy, childbirth, and the puerperium.... --- Walk 6 --- [DB99.7] Hepatic failure without mention whether acute or chronic --PARENT--> [DB99] 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.... --RELATED_TO--> [?] Liver disorders in pregnancy, childbirth or the puerperium Def: Any disorder affecting females, characterised by pathological changes to the liver that occur during pregnancy, childbirth, and the puerperium....
[ "[DB9Z] Diseases of liver, unspecified\n --PARENT--> [?] Diseases of liver\n --RELATED_TO--> [?] Structural developmental anomalies of liver", "[DB9Z] Diseases of liver, unspecified\n --PARENT--> [?] Diseases of liver\n --CHILD--> [DB90] Infectious liver disease", "[DB97.Z] Inflammatory liver disease, unspecified\n --PARENT--> [DB97] Certain specified inflammatory liver diseases\n --CHILD--> [DB97.2] Chronic hepatitis, not elsewhere classified", "[DB97.Z] Inflammatory liver disease, unspecified\n --PARENT--> [DB97] Certain specified inflammatory liver diseases\n --RELATED_TO--> [?] Hepatic sarcoidosis\n Def: This is a syndrome involving abnormal collections of chronic inflammatory cells (granulomas) that can form as nodules in multiple organs, of the liver....", "[DB99.7] Hepatic failure without mention whether acute or chronic\n --PARENT--> [DB99] 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....\n --RELATED_TO--> [?] Liver disorders in pregnancy, childbirth or the puerperium\n Def: Any disorder affecting females, characterised by pathological changes to the liver that occur during pregnancy, childbirth, and the puerperium....", "[DB99.7] Hepatic failure without mention whether acute or chronic\n --PARENT--> [DB99] 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....\n --RELATED_TO--> [?] Liver disorders in pregnancy, childbirth or the puerperium\n Def: Any disorder affecting females, characterised by pathological changes to the liver that occur during pregnancy, childbirth, and the puerperium...." ]
DB9Z
Diseases of liver, unspecified
[ { "from_icd11": "DB9Z", "icd10_code": "K7681", "icd10_title": "Hepatopulmonary syndrome" }, { "from_icd11": "DB9Z", "icd10_code": "K7689", "icd10_title": "Other specified diseases of liver" }, { "from_icd11": "DB9Z", "icd10_code": "K769", "icd10_title": "Liver disease, unspecified" }, { "from_icd11": "DB9Z", "icd10_code": "K77", "icd10_title": "Liver disorders in diseases classified elsewhere" }, { "from_icd11": "DB9Z", "icd10_code": "K762", "icd10_title": "Central hemorrhagic necrosis of liver" }, { "from_icd11": "DB9Z", "icd10_code": "K70-K77", "icd10_title": "" }, { "from_icd11": "DB9Z", "icd10_code": "K778", "icd10_title": "" }, { "from_icd11": "DB9Z", "icd10_code": "K72", "icd10_title": "Hepatic failure, not elsewhere classified" }, { "from_icd11": "DB9Z", "icd10_code": "K76", "icd10_title": "Other diseases of liver" }, { "from_icd11": "DB9Z", "icd10_code": "K768", "icd10_title": "Other specified diseases of liver" }, { "from_icd11": "DB97.Z", "icd10_code": "K7581", "icd10_title": "Nonalcoholic steatohepatitis (NASH)" }, { "from_icd11": "DB97.Z", "icd10_code": "K7589", "icd10_title": "Other specified inflammatory liver diseases" }, { "from_icd11": "DB97.Z", "icd10_code": "K759", "icd10_title": "Inflammatory liver disease, unspecified" }, { "from_icd11": "DB97.Z", "icd10_code": "K752", "icd10_title": "Nonspecific reactive hepatitis" }, { "from_icd11": "DB97.Z", "icd10_code": "K75", "icd10_title": "Other inflammatory liver diseases" } ]
K7681
Hepatopulmonary syndrome
We performed emergency surgery through a median sternotomy under general anesthesia. After systemic heparinization, cardiopulmonary bypass was established by arterial cannulation through the left common femoral artery and placement of a dual-stage venous cannula through the right atrium. A left heart drainage tube was inserted into the right superior pulmonary vein, and cardiopulmonary bypass was initiated. The ascending aorta was clamped at the end and incised, the new intimal flap was placed at the tip of the proximal bare spring, and the dissection extended into the aortic sinus . Protection of the myocardium was achieved by the intermittent infusion of a cardioplegia solution every 30 minutes. When the aortic valves were exposed, the aortic leaflets were resected. Then, a size-matched prosthetic valve conduit was selected and attached to the annulus with pledged-reinforced horizontal mattress sutures of 2–0 braided polyester. The coronary artery was subsequently anastomosed with the graft using continuous sutures of 5–0 polypropylene. The steel wires of the bare spring were cut to create an appropriate distal plane . The prosthetic graft was anastomosed with the previous endograft and the native ascending aortic wall , which was reinforced using a felt strip. The aorta was wrapped and sutured to the pericardium . The patient was then weaned off cardiopulmonary bypass, and the chest was closed.
3.976563
0.945313
sec[1]/p[2]
en
0.999998
PMC9351882
https://doi.org/10.1097/MD.0000000000029615
[ "aortic", "cardiopulmonary", "bypass", "artery", "ascending", "aorta", "bare", "spring", "prosthetic", "reinforced" ]
[ { "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": "MC82.4", "title": "Cardiopulmonary arrest" }, { "code": "1D62.1", "title": "Hantavirus pulmonary syndrome" }, { "code": "7A42.0", "title": "Obesity hypoventilation syndrome" }, { "code": "BC42.Z/4A42.Z", "title": "Myocarditis, unspecified [Systemic sclerosis with lung involvement]" }, { "code": "BC44&XA6WC4", "title": "Noncompaction cardiomyopathy [Pulmonary valve]" } ]
=== 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 [MC82.4] Cardiopulmonary arrest Also known as: Cardiopulmonary arrest | cardiopulmonary collapse | cardiorespiratory arrest | acute cardiopulmonary arrest | cardiopulmonary failure [1D62.1] Hantavirus pulmonary syndrome Definition: A disease of the respiratory system, caused by infection with certain hantaviruses. This disease is characterised by fever, fatigue, myalgia, headache, chills, nausea, vomiting, diarrhoea, or abdominal pain. This disease may also present with coughing and dyspnoea. Transmission is by the faecal-oral route or airborne transmission. Also known as: Hantavirus pulmonary syndrome | Hantavirus cardiopulmonary syndrome | HPS – [Hantavirus pulmonary syndrome] | HCPS – [Hantavirus cardiopulmonary syndrome] [7A42.0] Obesity hypoventilation syndrome Definition: Obesity hypoventilation syndrome is characterised by obesity (in adults, Body-Mass-Index > 30 kg/m²) and daytime hypercapnia indicated by arterial partial pressure of carbon dioxide (PaCO2) > 45 mm Hg that cannot be fully attributed to an underlying cardiopulmonary or neurologic disease. Hypercapnia worsens during sleep and is often associated with severe arterial oxygen desaturation. Obstructive sleep apnoea is also present in the majority of cases and should be diagnosed in addition to obesity Also known as: Obesity hypoventilation syndrome | Pickwickian syndrome | cardiopulmonary obesity syndrome | alveolar hypoventilation syndrome | alveolus hypoventilation syndrome Includes: Pickwickian syndrome === GRAPH WALKS === --- Walk 1 --- [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 2 --- [BD5Z] Diseases of arteries or arterioles, unspecified --PARENT--> [?] Diseases of arteries or arterioles --CHILD--> [BD30] Acute arterial occlusion --- 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... --PARENT--> [LA8A] 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.... --CHILD--> [LA8A.1] Congenital pulmonary atresia Def: A congenital cardiovascular malformation in which there is no opening between any ventricle and the pulmonary arterial tree.... --- 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... --PARENT--> [LA8A] 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.... --CHILD--> [LA8A.2] 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 --CHILD--> [BD40.2] Atherosclerosis of renal artery --- 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 --EXCLUDES--> [?] Diseases of coronary artery\n Def: Conditions affecting the blood perfusion of the heart....", "[BD5Z] Diseases of arteries or arterioles, unspecified\n --PARENT--> [?] Diseases of arteries or arterioles\n --CHILD--> [BD30] Acute arterial occlusion", "[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 --PARENT--> [LA8A] 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....\n --CHILD--> [LA8A.1] Congenital pulmonary atresia\n Def: A congenital cardiovascular malformation in which there is no opening between any ventricle and the pulmonary arterial tree....", "[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 --PARENT--> [LA8A] 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....\n --CHILD--> [LA8A.2] 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 --CHILD--> [BD40.2] Atherosclerosis of renal artery", "[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
Following recovery from chemotherapy, the patient underwent exploratory laparotomy with resection of the abdominal tumor, including en bloc antrectomy and segment IVb liver with Billroth II gastrojejunostomy reconstruction. The tumor was noted to be well-encapsulated clinically and pathologically. The gross specimen showed an 11x10 x 8 cm mass involving the liver parenchyma with 90% tumor necrosis. The histology demonstrated round, epithelioid, and spindle tumor cells arranged in an organoid pattern. There is a prominent vasculature. The immunostain workup showed the tumor cells were positive for synaptophysin but negative for cytokeratin AE1/AE3/CAM5.2, chromogranin, INSMS1, GATA3, inhibin, calretinin, c-MYC, desmin, MDM2, CDK4, CD117, DOG1, NXK2.2, WT1-1, ERG, CD99, S-100, SOX10, HMB45, and STAT6. SDHB was retained. The Ki-67 proliferation index was 20% by manual morphometric analysis. The EWSR1 and SS18 gene rearrangement testing by fluorescence in situ hybridization was also negative. Similar to the biopsy specimen, these largely negative findings did not support a diagnosis of neuroendocrine tumor, melanoma, dedifferentiated liposarcoma, gastrointestinal stromal tumor, angiosarcoma, Ewing sarcoma, desmoplastic small round cell tumor, solitary fibrous tumor, or adrenal tumor., etc, and therefore were suggestive of UPS. There was no angiolymphatic invasion. Surgical margins were free of tumors.
4.09375
0.96875
sec[1]/p[4]
en
0.999999
PMC9696860
https://doi.org/10.7759/cureus.30718
[ "tumor", "liver", "specimen", "round", "cells", "recovery", "chemotherapy", "exploratory", "laparotomy", "resection" ]
[ { "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": "DB9Z", "title": "Diseases of liver, unspecified" }, { "code": "DB97.Z", "title": "Inflammatory liver disease, unspecified" }, { "code": "DB99.7", "title": "Hepatic failure without mention whether acute or chronic" }, { "code": "LB20.0Y", "title": "Other specified structural developmental anomalies of liver" }, { "code": "LB20.0Z", "title": "Structural developmental anomalies of liver, unspecified" } ]
=== ICD-11 CODES FOUND === [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 [DB9Z] Diseases of liver, unspecified Also known as: Diseases of liver, unspecified | liver disease | liver condition NOS | organ liver disease | hepatopathy [DB97.Z] Inflammatory liver disease, unspecified Also known as: Inflammatory liver disease, unspecified | Certain specified inflammatory liver diseases | Nonspecific reactive hepatitis | inflammatory liver disease | hepatitis NOS [DB99.7] Hepatic failure without mention whether acute or chronic Also known as: Hepatic failure without mention whether acute or chronic | liver decompensation | liver function failure | hepatic failure NOS | liver failure NOS [LB20.0Y] Other specified structural developmental anomalies of liver Also known as: Other specified structural developmental anomalies of liver | Alagille syndrome | Alagille-Watson syndrome | Arteriohepatic dysplasia | Syndromic bile duct paucity [LB20.0Z] Structural developmental anomalies of liver, unspecified Also known as: Structural developmental anomalies of liver, unspecified | Structural developmental anomalies of liver | Malformations of liver | congenital anomaly of liver | congenital malformation of liver === GRAPH WALKS === --- Walk 1 --- [2F9Z] Neoplasms of unknown behaviour of unspecified site --PARENT--> [?] Neoplasms of unknown behaviour, except of lymphoid, haematopoietic, central nervous system or related tissues --CHILD--> [2F92] Neoplasms of unknown behaviour of skin --- Walk 2 --- [2F9Z] Neoplasms of unknown behaviour of unspecified site --PARENT--> [?] Neoplasms of unknown behaviour, except of lymphoid, haematopoietic, central nervous system or related tissues --RELATED_TO--> [?] Pathological fracture in neoplastic disease of unknown behaviour --- Walk 3 --- [ME61] Subcutaneous swelling, mass or lump of uncertain or unspecified nature Def: One or more localised subcutaneous soft tissue masses of undetermined or unspecified nature... --EXCLUDES--> [?] Localised adiposity Def: A condition characterised by accumulation of adipose tissue in specific regions of the body.... --PARENT--> [?] Overweight or localised adiposity Def: Overweight is a condition characterized by excessive adiposity. Overweight is assessed by the body mass index (BMI), which is a surrogate marker of adiposity calculated as weight (kg)/height² (m²). Th... --- 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--> [?] Enlarged lymph nodes Def: Enlarged lymph node is called lymphadenopathy which means the abnormal enlargement of lymph nodes.... --EXCLUDES--> [?] Lymphadenitis --- Walk 5 --- [2E6Z] Carcinoma in situ of unspecified site --PARENT--> [?] In situ neoplasms, except of lymphoid, haematopoietic, central nervous system or related tissues --CHILD--> [2E60] Carcinoma in situ of oral cavity, oesophagus or stomach --- Walk 6 --- [2E6Z] Carcinoma in situ of unspecified site --PARENT--> [?] In situ neoplasms, except of lymphoid, haematopoietic, central nervous system or related tissues --CHILD--> [2E62] Carcinoma in situ of middle ear or respiratory system
[ "[2F9Z] Neoplasms of unknown behaviour of unspecified site\n --PARENT--> [?] Neoplasms of unknown behaviour, except of lymphoid, haematopoietic, central nervous system or related tissues\n --CHILD--> [2F92] Neoplasms of unknown behaviour of skin", "[2F9Z] Neoplasms of unknown behaviour of unspecified site\n --PARENT--> [?] Neoplasms of unknown behaviour, except of lymphoid, haematopoietic, central nervous system or related tissues\n --RELATED_TO--> [?] Pathological fracture in neoplastic disease of unknown behaviour", "[ME61] Subcutaneous swelling, mass or lump of uncertain or unspecified nature\n Def: One or more localised subcutaneous soft tissue masses of undetermined or unspecified nature...\n --EXCLUDES--> [?] Localised adiposity\n Def: A condition characterised by accumulation of adipose tissue in specific regions of the body....\n --PARENT--> [?] Overweight or localised adiposity\n Def: Overweight is a condition characterized by excessive adiposity. Overweight is assessed by the body mass index (BMI), which is a surrogate marker of adiposity calculated as weight (kg)/height² (m²). Th...", "[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--> [?] Lymphadenitis", "[2E6Z] Carcinoma in situ of unspecified site\n --PARENT--> [?] In situ neoplasms, except of lymphoid, haematopoietic, central nervous system or related tissues\n --CHILD--> [2E60] Carcinoma in situ of oral cavity, oesophagus or stomach", "[2E6Z] Carcinoma in situ of unspecified site\n --PARENT--> [?] In situ neoplasms, except of lymphoid, haematopoietic, central nervous system or related tissues\n --CHILD--> [2E62] Carcinoma in situ of middle ear or respiratory system" ]
2F9Z
Neoplasms of unknown behaviour of unspecified site
[ { "from_icd11": "2F9Z", "icd10_code": "D487", "icd10_title": "Neoplasm of uncertain behavior of other specified sites" }, { "from_icd11": "2F9Z", "icd10_code": "D482", "icd10_title": "Neoplasm of uncertain behavior of peripheral nerves and autonomic nervous system" }, { "from_icd11": "2F9Z", "icd10_code": "D37-D48", "icd10_title": "" }, { "from_icd11": "2F9Z", "icd10_code": "D377", "icd10_title": "" }, { "from_icd11": "2F9Z", "icd10_code": "D48", "icd10_title": "Neoplasm of uncertain behavior of other and unspecified sites" }, { "from_icd11": "2F9Z", "icd10_code": "D489", "icd10_title": "Neoplasm of uncertain behavior, unspecified" }, { "from_icd11": "ME61", "icd10_code": "R2240", "icd10_title": "Localized swelling, mass and lump, unspecified lower limb" }, { "from_icd11": "ME61", "icd10_code": "R2232", "icd10_title": "Localized swelling, mass and lump, left upper limb" }, { "from_icd11": "ME61", "icd10_code": "R2242", "icd10_title": "Localized swelling, mass and lump, left lower limb" }, { "from_icd11": "ME61", "icd10_code": "R2231", "icd10_title": "Localized swelling, mass and lump, right upper limb" }, { "from_icd11": "ME61", "icd10_code": "R2241", "icd10_title": "Localized swelling, mass and lump, right lower limb" }, { "from_icd11": "ME61", "icd10_code": "R2233", "icd10_title": "Localized swelling, mass and lump, upper limb, bilateral" }, { "from_icd11": "ME61", "icd10_code": "R2243", "icd10_title": "Localized swelling, mass and lump, lower limb, bilateral" }, { "from_icd11": "ME61", "icd10_code": "R2230", "icd10_title": "Localized swelling, mass and lump, unspecified upper limb" }, { "from_icd11": "ME61", "icd10_code": "R220", "icd10_title": "Localized swelling, mass and lump, head" } ]
D487
Neoplasm of uncertain behavior of other specified sites
Our patient suffered from recurring severe non-specific abdominal pains for about five years, causing several hospital stays and two laparoscopic interventions. Approximately one year before admission to our hospital the patient developed ascites. Eosinophilic ascites is only observed in 10 % of cases. It indicates the involvement of the tunica serosa and is typical in women of childbearing age. Laparoscopy showed a swollen intestinal tract and lymph nodes resembling the aspect of intestinal tuberculosis. Thus ascites was screened for mycobacteria. One pcr screening turned out positive. Microscopy and repeated cultures from ascites, sputum and biopsy of intestinal lymph nodes remained negative for mycobacteria at all times. Lacking another coherent differential diagnosis anti mycobacterial treatment was started. Despite therapy for six month ascites and abdominal complaints remained nearly unchanged. On admission no signs of active tuberculosis were found. Skin test, chest x-ray, double pcr screening as well as cultures from sputum and ascites were negative. These findings raise the question if the tuberculosis has been treated successfully or the first pcr result has been false positive. Regarding the persisting symptoms the latter seems more probable. Furthermore international guidelines do not accept the single use of nucleic acid amplification technique to establish the diagnosis tuberculosis.
4.007813
0.977539
sec[2]/p[2]
en
0.999997
16026609
https://doi.org/10.1186/1471-230X-5-24
[ "ascites", "tuberculosis", "intestinal", "abdominal", "lymph", "nodes", "mycobacteria", "screening", "cultures", "sputum" ]
[ { "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": "1B1Z", "title": "Tuberculosis, unspecified" }, { "code": "1B1Y", "title": "Other specified tuberculosis" }, { "code": "KA61.0", "title": "Congenital tuberculosis" }, { "code": "1B12.40", "title": "Tuberculosis of bones or joints" }, { "code": "1B10.Z", "title": "Respiratory tuberculosis, without mention of bacteriological or histological confirmation" } ]
=== 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 [1B1Z] Tuberculosis, unspecified Also known as: Tuberculosis, unspecified | Infections due to Mycobacterium tuberculosis and Mycobacterium bovis | TB - [tuberculosis] | Tuberculosis infection | TBC - [tuberculosis] [1B1Y] Other specified tuberculosis Also known as: Other specified tuberculosis | Disorders of kidney or ureter in tuberculosis [KA61.0] Congenital tuberculosis Definition: A disease affecting infants, caused by an infection with the bacteria Mycobacterium tuberculosis in utero. Transmission is by vertical transmission. Also known as: Congenital tuberculosis | congenital tuberculous gangrene | congenital tuberculous degeneration | congenital necrotic tuberculosis | congenital tuberculous infection [1B12.40] Tuberculosis of bones or joints Definition: A disease of the bones and joints, caused by an infection with the bacteria Mycobacterium tuberculosis. This disease commonly presents with bone pain, joint inflammation, loss of movement or feeling in the affected bone or joint, and weak bones prone to fracture. Transmission is through haematogenous spread to the bones and joints after inhalation of infected respiratory secretions. Confirmation is by identification of Mycobacterium tuberculosis in biopsy samples of the affected site. Also known as: Tuberculosis of bones or joints | tuberculous cartilage | tuberculosis of bone | tuberculosis of joint | tuberculous bone [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 === 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.Y] Other specified ascites --- 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.Y] Other specified ascites --- 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--> [ME04.0] Fluid in peritoneal cavity --- 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--> [DC51.1] Peritoneal adhesions Def: Disorders of peritoneum sticking by scar tissue or fibrosis... --- 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 --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...
[ "[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.Y] Other specified ascites", "[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.Y] Other specified ascites", "[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", "[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--> [DC51.1] Peritoneal adhesions\n Def: Disorders of peritoneum sticking by scar tissue or fibrosis...", "[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..." ]
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
On 7th February 2012 (at the 34 +4th GW), no fetal movement was observed, and a non-reaction type of NST was presented. The baseline of FHR was 145 beats per minute, without obvious FHR fluctuation even during HD. Intrauterine fetal distress was highly suspected, and so we decided to cease the pregnancy immediately. On that day, the patient underwent caesarean section and was delivered of a female, well-being baby weighing 1470 g. The Apgar score was 5, 8 and 9 at the 1st, 5th and 10th minutes respectively. The placenta was pathologically examined , and the result revealed placental dysfunction, single umbilical artery and vascular pathological change caused by hypertension. Fig. 2 Placenta and its pathological examination. a Placenta by naked eyes. The volume is 18 × 13 × (1.5–2) cm, with sections of dull-red color and complete placental membrane, no cyst can be found. b Chorionic villi of placenta under microscope (HE × 200). Mild edema and increased syncytial cell nodules can be seen in partial villi, indicating placental dysfunction. c A chorionic blood vessel under microscope (HE × 400). Chorionic blood vessel presents hyaline degeneration and fibrous necrosis, according with the diagnosis of hypertension. d Umbilical artery under microscope (HE × 400). There is only one artery in umbilical cord, with a thickened wall and a narrow lumen, according with the diagnosis of single umbilical artery
3.892578
0.979004
sec[1]/sec[4]/p[1]
en
0.999997
26370296
https://doi.org/10.1186/s12884-015-0642-9
[ "placenta", "umbilical", "artery", "placental", "chorionic", "microscope", "fetal", "dysfunction", "single", "pathological" ]
[ { "code": "JA8A.1", "title": "Malformation of placenta" }, { "code": "JA8A.Y", "title": "Other specified maternal care related to placental disorders" }, { "code": "JA8B.Z", "title": "Maternal care related to placenta praevia or low lying placenta, unspecified" }, { "code": "JA86.4", "title": "Maternal care for fetal growth restriction" }, { "code": "2F96&XA90F8", "title": "Neoplasms of unknown behaviour of placenta" }, { "code": "LB03.Y", "title": "Other specified structural developmental anomalies of umbilical cord" }, { "code": "MD82", "title": "Intra-abdominal or pelvic swelling, mass or lump" }, { "code": "LB03.Z", "title": "Structural developmental anomalies of umbilical cord, unspecified" }, { "code": "LB03.1", "title": "Single umbilical cord artery" }, { "code": "DD53", "title": "Umbilical hernia" } ]
=== ICD-11 CODES FOUND === [JA8A.1] Malformation of placenta Also known as: Malformation of placenta | variation of placenta form | deformity of placenta | placental deformity | Abnormal placenta NOS [JA8A.Y] Other specified maternal care related to placental disorders Also known as: Other specified maternal care related to placental disorders | Obliteration of placental blood vessels | Placenta dysfunction syndrome | placental dysfunction syndrome | placental dysfunction [JA8B.Z] Maternal care related to placenta praevia or low lying placenta, unspecified Also known as: Maternal care related to placenta praevia or low lying placenta, unspecified | Maternal care related to placenta praevia or low lying placenta | lateral placenta | total placenta previa | PP - [placenta previa] [JA86.4] Maternal care for fetal growth restriction Also known as: Maternal care for fetal growth restriction | maternal care for intrauterine growth retardation | Maternal care for known or suspected: small-for-gestational age | intrauterine growth retardation affecting management of pregnancy | light-for-dates affecting management of pregnancy [LB03.Y] Other specified structural developmental anomalies of umbilical cord Also known as: Other specified structural developmental anomalies of umbilical cord | Umbilical cord calcifications | Omphalomesenteric duct remnants or cysts | Vitelline duct remnants and cysts | Persistent omphalomesenteric duct [MD82] Intra-abdominal or pelvic swelling, mass or lump Definition: This refers to the presence of abdominal or pelvic wall swelling, mass or tumour in the abdominal and pelvic regions. These mass or tumours can be recognised by visual examination and/or palpation. Also known as: Intra-abdominal or pelvic swelling, mass or lump | Abdominal mass without further specification | mass in abdomen | intra-abdominal lump | intra-abdominal mass Excludes: Abdominal distension | Ascites [LB03.Z] Structural developmental anomalies of umbilical cord, unspecified Also known as: Structural developmental anomalies of umbilical cord, unspecified | Structural developmental anomalies of umbilical cord | Malformations of umbilical cord [LB03.1] Single umbilical cord artery Definition: A single umbilical artery arising from either the allantoic arterial system (Type I) or vitelline artery (Type II). It has been associated with renal anomalies. Also known as: Single umbilical cord artery | Congenital absence and hypoplasia of umbilical artery | congenital absence of umbilical artery | congenital hypoplasia of umbilical artery | umbilical artery hypoplasia [DD53] Umbilical hernia Definition: A hernia occurs when part of an internal organ bulges through a weak area of muscle. An umbilical hernia is a protrusion of the peritoneum and fluid, omentum, or a portion of abdominal organ(s) through the umbilical ring. The umbilical ring is the fibrous and muscle tissue around the navel (belly-button). Small hernias usually close spontaneously without treatment by age 1 or 2. Umbilical hernias are usually painless and are common in infants. Also known as: Umbilical hernia | Umbilical hernia with obstruction, without gangrene | incarcerated umbilical hernia without gangrene | irreducible umbilical hernia without gangrene | Umbilical hernia causing obstruction without gangrene Excludes: Omphalocele | Urachal cyst === GRAPH WALKS === --- Walk 1 --- [JA8A.1] Malformation of placenta --PARENT--> [JA8A] Maternal care related to placental disorders --CHILD--> [JA8A.1] Malformation of placenta --- Walk 2 --- [JA8A.1] Malformation of placenta --PARENT--> [JA8A] Maternal care related to placental disorders --EXCLUDES--> [?] Maternal care related to placenta praevia or low lying placenta Def: A placenta that is implanted over or very near the internal cervical os--total, partial, marginal, low-lying placenta... --- Walk 3 --- [JA8A.Y] Other specified maternal care related to placental disorders --PARENT--> [JA8A] Maternal care related to placental disorders --EXCLUDES--> [?] Maternal care related to premature separation of placenta --- Walk 4 --- [JA8A.Y] Other specified maternal care related to placental disorders --PARENT--> [JA8A] Maternal care related to placental disorders --EXCLUDES--> [?] Maternal care related to premature separation of placenta --- Walk 5 --- [JA8B.Z] Maternal care related to placenta praevia or low lying placenta, unspecified --PARENT--> [JA8B] Maternal care related to placenta praevia or low lying placenta Def: A placenta that is implanted over or very near the internal cervical os--total, partial, marginal, low-lying placenta... --PARENT--> [?] Maternal care related to the fetus, amniotic cavity or possible delivery problems Def: A group of conditions characterised by the provision of health interventions to the mother due to conditions associated with the fetus, the amniotic cavity, or to issues associated with labour and del... --- Walk 6 --- [JA8B.Z] Maternal care related to placenta praevia or low lying placenta, unspecified --PARENT--> [JA8B] Maternal care related to placenta praevia or low lying placenta Def: A placenta that is implanted over or very near the internal cervical os--total, partial, marginal, low-lying placenta... --CHILD--> [JA8B.0] Placenta praevia specified as without haemorrhage
[ "[JA8A.1] Malformation of placenta\n --PARENT--> [JA8A] Maternal care related to placental disorders\n --CHILD--> [JA8A.1] Malformation of placenta", "[JA8A.1] Malformation of placenta\n --PARENT--> [JA8A] Maternal care related to placental disorders\n --EXCLUDES--> [?] Maternal care related to placenta praevia or low lying placenta\n Def: A placenta that is implanted over or very near the internal cervical os--total, partial, marginal, low-lying placenta...", "[JA8A.Y] Other specified maternal care related to placental disorders\n --PARENT--> [JA8A] Maternal care related to placental disorders\n --EXCLUDES--> [?] Maternal care related to premature separation of placenta", "[JA8A.Y] Other specified maternal care related to placental disorders\n --PARENT--> [JA8A] Maternal care related to placental disorders\n --EXCLUDES--> [?] Maternal care related to premature separation of placenta", "[JA8B.Z] Maternal care related to placenta praevia or low lying placenta, unspecified\n --PARENT--> [JA8B] Maternal care related to placenta praevia or low lying placenta\n Def: A placenta that is implanted over or very near the internal cervical os--total, partial, marginal, low-lying placenta...\n --PARENT--> [?] Maternal care related to the fetus, amniotic cavity or possible delivery problems\n Def: A group of conditions characterised by the provision of health interventions to the mother due to conditions associated with the fetus, the amniotic cavity, or to issues associated with labour and del...", "[JA8B.Z] Maternal care related to placenta praevia or low lying placenta, unspecified\n --PARENT--> [JA8B] Maternal care related to placenta praevia or low lying placenta\n Def: A placenta that is implanted over or very near the internal cervical os--total, partial, marginal, low-lying placenta...\n --CHILD--> [JA8B.0] Placenta praevia specified as without haemorrhage" ]
JA8A.1
Malformation of placenta
[ { "from_icd11": "JA8A.1", "icd10_code": "O43123", "icd10_title": "Velamentous insertion of umbilical cord, third trimester" }, { "from_icd11": "JA8A.1", "icd10_code": "O43193", "icd10_title": "Other malformation of placenta, third trimester" }, { "from_icd11": "JA8A.1", "icd10_code": "O43122", "icd10_title": "Velamentous insertion of umbilical cord, second trimester" }, { "from_icd11": "JA8A.1", "icd10_code": "O43113", "icd10_title": "Circumvallate placenta, third trimester" }, { "from_icd11": "JA8A.1", "icd10_code": "O43192", "icd10_title": "Other malformation of placenta, second trimester" }, { "from_icd11": "JA8A.1", "icd10_code": "O43103", "icd10_title": "Malformation of placenta, unspecified, third trimester" }, { "from_icd11": "JA8A.1", "icd10_code": "O43101", "icd10_title": "Malformation of placenta, unspecified, first trimester" }, { "from_icd11": "JA8A.1", "icd10_code": "O43102", "icd10_title": "Malformation of placenta, unspecified, second trimester" }, { "from_icd11": "JA8A.1", "icd10_code": "O431", "icd10_title": "Malformation of placenta" }, { "from_icd11": "JA8B.Z", "icd10_code": "O4443", "icd10_title": "Low lying placenta NOS or without hemorrhage, third trimester" }, { "from_icd11": "JA8B.Z", "icd10_code": "O4452", "icd10_title": "Low lying placenta with hemorrhage, second trimester" }, { "from_icd11": "JA8B.Z", "icd10_code": "O4442", "icd10_title": "Low lying placenta NOS or without hemorrhage, second trimester" }, { "from_icd11": "JA8B.Z", "icd10_code": "O4423", "icd10_title": "Partial placenta previa NOS or without hemorrhage, third trimester" }, { "from_icd11": "JA8B.Z", "icd10_code": "O4453", "icd10_title": "Low lying placenta with hemorrhage, third trimester" }, { "from_icd11": "JA8B.Z", "icd10_code": "O44", "icd10_title": "Placenta previa" } ]
O43123
Velamentous insertion of umbilical cord, third trimester
Our case is a female patient, born to a 28-year-old mother. This was the mother's first pregnancy. The mother denied any antenatal problems, and the baby was born vaginally at full term. Family history revealed no interrelative marriage or history of congenital malformation. Results of a chromosomal analysis showed a normal female. The baby was born with severe nasal deformation. On gross inspection the external nose was absent. The nasal dorsum structures and remnants of the alar cartilages were barely palpable. The columella and right nostril were absent; the left nostril was severely stenotic . Probing and dilating revealed a small cul-de-sac. Submucosal cleft palate, right auricular deformity, and hypotelorism were also present. Axial computerized tomography showed that the nasal and paranasal structures were not developed . A cul-de sac was present in place of the intranasal structures. Intracranial midline structures such as the septum pellucidum, falx cerebri, corpus callosum, and third ventricle were absent. The lateral ventricles and the third ventricle were replaced by a monoventricle. Cerebral hemispherical cortical sulci and a sylvian fissure were not observed. A 7-cm posterior intracranial cyst was present. These findings were consistent with alobar holoprosencephaly. The family declined any surgical intervention such as tracheotomy, and the patient was discharged with an oral airway.
3.865234
0.986328
sec[1]/p[0]
en
0.999998
17883831
https://doi.org/10.1186/1752-1947-1-97
[ "structures", "born", "mother", "nasal", "absent", "present", "baby", "family", "nostril", "intracranial" ]
[ { "code": "LD0Z", "title": "Structural developmental anomalies primarily affecting one body system, unspecified" }, { "code": "FA7Z", "title": "Structural disorders of spine, unspecified" }, { "code": "LD24.Z", "title": "Syndromes with skeletal anomalies as a major feature, unspecified" }, { "code": "FA7Y", "title": "Other specified structural disorders of spine" }, { "code": "QF0Z", "title": "Acquired absence of body structure, unspecified" }, { "code": "QA46.0", "title": "Single live birth" }, { "code": "QA47.2", "title": "Singleton, unspecified as to place of birth" }, { "code": "QA47.3Z", "title": "Twin, born in hospital, unspecified" }, { "code": "1D4Z", "title": "Arthropod-borne viral fever, virus unspecified" }, { "code": "1A1Z", "title": "Bacterial foodborne intoxications, unspecified" } ]
=== ICD-11 CODES FOUND === [LD0Z] Structural developmental anomalies primarily affecting one body system, unspecified Also known as: Structural developmental anomalies primarily affecting one body system, unspecified | Structural malformations [FA7Z] Structural disorders of spine, unspecified Also known as: Structural disorders of spine, unspecified | spinal disease [LD24.Z] Syndromes with skeletal anomalies as a major feature, unspecified Also known as: Syndromes with skeletal anomalies as a major feature, unspecified | Syndromes with skeletal anomalies as a major feature | Structural bone dysplasias [FA7Y] Other specified structural disorders of spine Also known as: Other specified structural disorders of spine [QF0Z] Acquired absence of body structure, unspecified Also known as: Acquired absence of body structure, unspecified [QA46.0] Single live birth Definition: Live birth is the complete expulsion or extraction from a woman of a fetus, irrespective of the duration of the pregnancy, which, after such separation, shows signs of life. Also known as: Single live birth | single liveborn | outcome of delivery of single liveborn [QA47.2] Singleton, unspecified as to place of birth Also known as: Singleton, unspecified as to place of birth | liveborn infant NOS | newborn infant NOS | newborn NOS [QA47.3Z] Twin, born in hospital, unspecified Also known as: Twin, born in hospital, unspecified | Twin, born in hospital | twin liveborn infant born in hospital | newborn twin, born in hospital [1D4Z] Arthropod-borne viral fever, virus unspecified Also known as: Arthropod-borne viral fever, virus unspecified | Tick-borne viral fevers | Mosquito-borne viral fevers | mosquito-borne fever | arboviral disease [1A1Z] Bacterial foodborne intoxications, unspecified Also known as: Bacterial foodborne intoxications, unspecified | food contamination | bacterial ichthyotoxism | bacterial fish poisoning | epidemic bacterial fish poisoning === GRAPH WALKS === --- Walk 1 --- [LD0Z] Structural developmental anomalies primarily affecting one body system, unspecified --PARENT--> [?] Structural developmental anomalies primarily affecting one body system Def: A deformation established before birth of an anatomical structure.... --CHILD--> [?] Structural developmental anomalies of the ear Def: Any condition caused by failure of the ear to correctly develop during the antenatal period.... --- Walk 2 --- [LD0Z] Structural developmental anomalies primarily affecting one body system, unspecified --PARENT--> [?] Structural developmental anomalies primarily affecting one body system Def: A deformation established before birth of an anatomical structure.... --CHILD--> [?] 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 3 --- [FA7Z] Structural disorders of spine, unspecified --PARENT--> [?] Structural disorders of spine --CHILD--> [FA70] Spinal deformities --- Walk 4 --- [FA7Z] Structural disorders of spine, unspecified --PARENT--> [?] Structural disorders of spine --CHILD--> [FA72] Disorders of vertebra Def: Changes in the structure of the spine causing damage to vertebrae and surrounding tissue secondary to infection, injury, tumours, infections, bone changes that come with age etc. Spinal diseases often... --- Walk 5 --- [LD24.Z] Syndromes with skeletal anomalies as a major feature, unspecified --PARENT--> [LD24] Syndromes with skeletal anomalies as a major feature --RELATED_TO--> [?] Progressive osseous heteroplasia --- Walk 6 --- [LD24.Z] Syndromes with skeletal anomalies as a major feature, unspecified --PARENT--> [LD24] Syndromes with skeletal anomalies as a major feature --RELATED_TO--> [?] Progressive osseous heteroplasia
[ "[LD0Z] Structural developmental anomalies primarily affecting one body system, unspecified\n --PARENT--> [?] Structural developmental anomalies primarily affecting one body system\n Def: A deformation established before birth of an anatomical structure....\n --CHILD--> [?] Structural developmental anomalies of the ear\n Def: Any condition caused by failure of the ear to correctly develop during the antenatal period....", "[LD0Z] Structural developmental anomalies primarily affecting one body system, unspecified\n --PARENT--> [?] Structural developmental anomalies primarily affecting one body system\n Def: A deformation established before birth of an anatomical structure....\n --CHILD--> [?] 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....", "[FA7Z] Structural disorders of spine, unspecified\n --PARENT--> [?] Structural disorders of spine\n --CHILD--> [FA70] Spinal deformities", "[FA7Z] Structural disorders of spine, unspecified\n --PARENT--> [?] Structural disorders of spine\n --CHILD--> [FA72] Disorders of vertebra\n Def: Changes in the structure of the spine causing damage to vertebrae and surrounding tissue secondary to infection, injury, tumours, infections, bone changes that come with age etc. Spinal diseases often...", "[LD24.Z] Syndromes with skeletal anomalies as a major feature, unspecified\n --PARENT--> [LD24] Syndromes with skeletal anomalies as a major feature\n --RELATED_TO--> [?] Progressive osseous heteroplasia", "[LD24.Z] Syndromes with skeletal anomalies as a major feature, unspecified\n --PARENT--> [LD24] Syndromes with skeletal anomalies as a major feature\n --RELATED_TO--> [?] Progressive osseous heteroplasia" ]
LD0Z
Structural developmental anomalies primarily affecting one body system, unspecified
[ { "from_icd11": "LD0Z", "icd10_code": "Q6412", "icd10_title": "Cloacal exstrophy of urinary bladder" }, { "from_icd11": "LD0Z", "icd10_code": "Q6419", "icd10_title": "Other exstrophy of urinary bladder" }, { "from_icd11": "LD0Z", "icd10_code": "Q6410", "icd10_title": "Exstrophy of urinary bladder, unspecified" }, { "from_icd11": "LD0Z", "icd10_code": "Q791", "icd10_title": "Other congenital malformations of diaphragm" }, { "from_icd11": "LD0Z", "icd10_code": "Q688", "icd10_title": "Other specified congenital musculoskeletal deformities" }, { "from_icd11": "LD0Z", "icd10_code": "Q799", "icd10_title": "Congenital malformation of musculoskeletal system, unspecified" }, { "from_icd11": "LD0Z", "icd10_code": "Q892", "icd10_title": "Congenital malformations of other endocrine glands" }, { "from_icd11": "LD0Z", "icd10_code": "Q798", "icd10_title": "Other congenital malformations of musculoskeletal system" }, { "from_icd11": "LD0Z", "icd10_code": "Q188", "icd10_title": "Other specified congenital malformations of face and neck" }, { "from_icd11": "LD0Z", "icd10_code": "Q189", "icd10_title": "Congenital malformation of face and neck, unspecified" }, { "from_icd11": "LD0Z", "icd10_code": "Q674", "icd10_title": "Other congenital deformities of skull, face and jaw" }, { "from_icd11": "LD0Z", "icd10_code": "Q18", "icd10_title": "Other congenital malformations of face and neck" }, { "from_icd11": "LD0Z", "icd10_code": "Q67", "icd10_title": "Congenital musculoskeletal deformities of head, face, spine and chest" }, { "from_icd11": "LD0Z", "icd10_code": "Q68", "icd10_title": "Other congenital musculoskeletal deformities" }, { "from_icd11": "LD0Z", "icd10_code": "Q79", "icd10_title": "Congenital malformations of musculoskeletal system, not elsewhere classified" } ]
Q6412
Cloacal exstrophy of urinary bladder
Breast cancer (BC) is a common malignancy diagnosed in females and is considered a prime cause of death among women globally . Mortality is related to distant metastases formed mainly in the liver, bones, and lungs. Nearly 5 to 8 % of diagnosed patients have distant metastases . Moreover, bone metastases (BM) are present in 90 % of women with distant metastases and commonly recurrence after BC therapy . The main sites of BM include the vertebral column, the hip bone, and the proximal femur. However, the proximal femur has several locations for metastases formation; the neck, subtrochanteric, and intertrochanteric sites . These lesions result in bone pain and pathological fractures. Survival in BM patients may reach four years. Hence, early diagnosis and treatment relieve the patients' outcomes. Proximal femoral metastasis treatment aims to improve the quality of life (QoL), alleviate bone pain, and rehabilitate skeletal function . A cephalomedullary device (internal fixation) is the option in subtrochanteric fractures once the femoral head and neck can reinforce the implant . Besides, the proximal femoral nail (PFN) is an appropriate procedure as it reduces surgical dissection, bleeding, trauma, and postoperative complications . In this case, we report a subtrochanteric metastatic fracture fixed using PFN in a previously treated BC woman. This manuscript was prepared by the SCARE 2020 guidelines .
4.078125
0.898926
sec[0]/p[0]
en
0.999998
37354822
https://doi.org/10.1016/j.ijscr.2023.108411
[ "metastases", "bone", "distant", "patients", "subtrochanteric", "femoral", "diagnosed", "women", "sites", "femur" ]
[ { "code": "2E2Z", "title": "Malignant neoplasm metastasis, unspecified" }, { "code": "2E03", "title": "Malignant neoplasm metastasis in bone or bone marrow" }, { "code": "2E08", "title": "Metastatic malignant neoplasm involving skin" }, { "code": "2E0Y&XA25Q2", "title": "Malignant neoplasm metastasis in pelvic viscera" }, { "code": "2D8Y&XA1WN1", "title": "Malignant neoplasm metastasis in oral cavity" }, { "code": "FC0Z", "title": "Diseases of the musculoskeletal system or connective tissue, unspecified" }, { "code": "FB84.Z", "title": "Osteomyelitis or osteitis, unspecified" }, { "code": "FB80.Z", "title": "Disorder of bone density or structure, unspecified" }, { "code": "FB86.11", "title": "Hypertrophy of bone" }, { "code": "FB86.1Z", "title": "Bone hyperplasias, unspecified" } ]
=== ICD-11 CODES FOUND === [2E2Z] Malignant neoplasm metastasis, unspecified Also known as: Malignant neoplasm metastasis, unspecified | secondary malignant neoplasm | metastasis | metastases | disseminated metastases [2E03] Malignant neoplasm metastasis in bone or bone marrow Definition: The spread of a malignant neoplasm from a primary site to the skeletal system. The majority of metastatic neoplasms to the bone are carcinomas. Also known as: Malignant neoplasm metastasis in bone or bone marrow | bone metastasis | bony metastasis | osseous metastasis | secondary cancer of bone [2E08] Metastatic malignant neoplasm involving skin Definition: Involvement of the skin by metastatic spread from a known or unknown primary malignant neoplasm. The secondary deposit may result from local migration of malignant cells, or from regional lymphatic or haematogenous spread from more distant sites. Also known as: Metastatic malignant neoplasm involving skin | cutaneous metastasis | metastasis to skin, any site | skin metastasis | skin secondaries [FC0Z] Diseases of the musculoskeletal system or connective tissue, unspecified Also known as: Diseases of the musculoskeletal system or connective tissue, unspecified | bone disease NOS | bone disorder NOS | bone lesion NOS | musculoskeletal complications NOS [FB84.Z] Osteomyelitis or osteitis, unspecified Also known as: Osteomyelitis or osteitis, unspecified | Osteomyelitis or osteitis | bone inflammation | bone ulcer | bone inflammatory disease [FB80.Z] Disorder of bone density or structure, unspecified Also known as: Disorder of bone density or structure, unspecified | Certain specified disorders of bone density or structure [FB86.11] Hypertrophy of bone Also known as: Hypertrophy of bone | bone thickening | periosteum thickening | Infantile cortical hyperostoses | Post traumatic subperiosteal ossification [FB86.1Z] Bone hyperplasias, unspecified Also known as: Bone hyperplasias, unspecified | Bone hyperplasias === GRAPH WALKS === --- Walk 1 --- [2E2Z] Malignant neoplasm metastasis, unspecified --PARENT--> [?] Malignant neoplasm metastases Def: Spread of a malignant neoplasm into secondary sites.... --CHILD--> [2D52] Malignant neoplasm metastasis in spinal cord, cranial nerves or paraspinal nerves --- Walk 2 --- [2E2Z] Malignant neoplasm metastasis, unspecified --PARENT--> [?] Malignant neoplasm metastases Def: Spread of a malignant neoplasm into secondary sites.... --PARENT--> [?] Malignant neoplasms, except primary neoplasms of lymphoid, haematopoietic, central nervous system or related tissues --- Walk 3 --- [2E03] 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.... --PARENT--> [?] Malignant neoplasm metastasis in other specified sites --CHILD--> [2E00] Malignant neoplasm metastasis in kidney or renal pelvis Def: The spread of the cancer to the kidney. This may be from a primary kidney cancer involving the opposite kidney, or from a cancer at a distant site.... --- Walk 4 --- [2E03] 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.... --PARENT--> [?] Malignant neoplasm metastasis in other specified sites --CHILD--> [2E02] Malignant neoplasm metastasis in other or unspecified urinary system organs --- Walk 5 --- [2E08] Metastatic malignant neoplasm involving skin Def: Involvement of the skin by metastatic spread from a known or unknown primary malignant neoplasm. The secondary deposit may result from local migration of malignant cells, or from regional lymphatic or... --PARENT--> [?] Malignant neoplasm metastasis in other specified sites --CHILD--> [2E00] Malignant neoplasm metastasis in kidney or renal pelvis Def: The spread of the cancer to the kidney. This may be from a primary kidney cancer involving the opposite kidney, or from a cancer at a distant site.... --- Walk 6 --- [2E08] Metastatic malignant neoplasm involving skin Def: Involvement of the skin by metastatic spread from a known or unknown primary malignant neoplasm. The secondary deposit may result from local migration of malignant cells, or from regional lymphatic or... --PARENT--> [?] Malignant neoplasm metastasis in other specified sites --CHILD--> [2E02] Malignant neoplasm metastasis in other or unspecified urinary system organs
[ "[2E2Z] Malignant neoplasm metastasis, unspecified\n --PARENT--> [?] Malignant neoplasm metastases\n Def: Spread of a malignant neoplasm into secondary sites....\n --CHILD--> [2D52] Malignant neoplasm metastasis in spinal cord, cranial nerves or paraspinal nerves", "[2E2Z] Malignant neoplasm metastasis, unspecified\n --PARENT--> [?] Malignant neoplasm metastases\n Def: Spread of a malignant neoplasm into secondary sites....\n --PARENT--> [?] Malignant neoplasms, except primary neoplasms of lymphoid, haematopoietic, central nervous system or related tissues", "[2E03] 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....\n --PARENT--> [?] Malignant neoplasm metastasis in other specified sites\n --CHILD--> [2E00] Malignant neoplasm metastasis in kidney or renal pelvis\n Def: The spread of the cancer to the kidney. This may be from a primary kidney cancer involving the opposite kidney, or from a cancer at a distant site....", "[2E03] 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....\n --PARENT--> [?] Malignant neoplasm metastasis in other specified sites\n --CHILD--> [2E02] Malignant neoplasm metastasis in other or unspecified urinary system organs", "[2E08] Metastatic malignant neoplasm involving skin\n Def: Involvement of the skin by metastatic spread from a known or unknown primary malignant neoplasm. The secondary deposit may result from local migration of malignant cells, or from regional lymphatic or...\n --PARENT--> [?] Malignant neoplasm metastasis in other specified sites\n --CHILD--> [2E00] Malignant neoplasm metastasis in kidney or renal pelvis\n Def: The spread of the cancer to the kidney. This may be from a primary kidney cancer involving the opposite kidney, or from a cancer at a distant site....", "[2E08] Metastatic malignant neoplasm involving skin\n Def: Involvement of the skin by metastatic spread from a known or unknown primary malignant neoplasm. The secondary deposit may result from local migration of malignant cells, or from regional lymphatic or...\n --PARENT--> [?] Malignant neoplasm metastasis in other specified sites\n --CHILD--> [2E02] Malignant neoplasm metastasis in other or unspecified urinary system organs" ]
2E2Z
Malignant neoplasm metastasis, unspecified
[ { "from_icd11": "2E2Z", "icd10_code": "C7949", "icd10_title": "Secondary malignant neoplasm of other parts of nervous system" }, { "from_icd11": "2E2Z", "icd10_code": "C7932", "icd10_title": "Secondary malignant neoplasm of cerebral meninges" }, { "from_icd11": "2E2Z", "icd10_code": "C7982", "icd10_title": "Secondary malignant neoplasm of genital organs" }, { "from_icd11": "2E2Z", "icd10_code": "C7940", "icd10_title": "Secondary malignant neoplasm of unspecified part of nervous system" }, { "from_icd11": "2E2Z", "icd10_code": "C7981", "icd10_title": "Secondary malignant neoplasm of breast" }, { "from_icd11": "2E2Z", "icd10_code": "C799", "icd10_title": "Secondary malignant neoplasm of unspecified site" }, { "from_icd11": "2E2Z", "icd10_code": "C76-C80", "icd10_title": "" }, { "from_icd11": "2E2Z", "icd10_code": "C79", "icd10_title": "Secondary malignant neoplasm of other and unspecified sites" }, { "from_icd11": "2E2Z", "icd10_code": "C798", "icd10_title": "Secondary malignant neoplasm of other specified sites" }, { "from_icd11": "2E2Z", "icd10_code": "C793", "icd10_title": "Secondary malignant neoplasm of brain and cerebral meninges" }, { "from_icd11": "2E2Z", "icd10_code": "C794", "icd10_title": "Secondary malignant neoplasm of other and unspecified parts of nervous system" }, { "from_icd11": "2E03", "icd10_code": "C7952", "icd10_title": "Secondary malignant neoplasm of bone marrow" }, { "from_icd11": "2E03", "icd10_code": "C795", "icd10_title": "Secondary malignant neoplasm of bone and bone marrow" }, { "from_icd11": "2E08", "icd10_code": "C792", "icd10_title": "Secondary malignant neoplasm of skin" }, { "from_icd11": "FC0Z", "icd10_code": "XIII", "icd10_title": "" } ]
C7949
Secondary malignant neoplasm of other parts of nervous system
Our patient’s immune markers were elevated, with an erythrocyte sedimentation rate of 135 mm/h and C-reactive protein level of 96 mg/dL. Chest radiography showed bilateral mid-zone and lower-zone infiltrates with cavitation and small pleural effusions . Contrast-enhanced thoracic computed tomography confirmed the presence of multifocal alveolar infiltrates, cavitations, and effusions . A Mantoux test was not performed because she had undergone one previously, though the results were not available. Although a γ-interferon-release assay would have been useful, we did not have the facilities to perform this investigation. A sputum acid-fast bacilli (AFB) test was negative in three consecutive samples. The difference between her serum and pleural fluid protein levels was 15 g/L and the differential lymphocyte count was 70 %. Her lactate dehydrogenase level was 600 U/L in her pleural fluid. Results from cytology, Gram staining, AFB, and TB polymerase chain reaction and cultures of the pleural fluid were negative. Fig. 4 Chest radiography at presentation. Multiple nodular and cavitating lesions are visible predominately on the right side with multiple patchy infiltrates typical of granulomatosis with polyangiitis. Costophrenic angles are obliterated owing to small bi-basal pleural effusions Fig. 5 Contrast-enhanced thoracic computed tomography at presentation. Multifocal alveolar infiltrates are visible
4.015625
0.97168
sec[1]/sec[1]/p[0]
en
0.999995
26714880
https://doi.org/10.1186/s13256-015-0792-4
[ "pleural", "infiltrates", "effusions", "fluid", "protein", "chest", "radiography", "zone", "small", "contrast" ]
[ { "code": "CB2Z", "title": "Pleural, diaphragm or mediastinal disorders, unspecified" }, { "code": "LA76", "title": "Structural developmental anomalies of pleura" }, { "code": "MD31", "title": "Pleurisy" }, { "code": "NB32.60", "title": "Laceration of pleura" }, { "code": "2F91.Y&XA5TT2", "title": "Neoplasms of unknown behaviour of pleura" }, { "code": "MD41", "title": "Clinical findings on diagnostic imaging of lung" }, { "code": "GB90.Y", "title": "Other specified disorders of kidney or ureter" }, { "code": "DB9Z", "title": "Diseases of liver, unspecified" }, { "code": "9A78.2Z", "title": "Corneal oedema, unspecified" }, { "code": "FB32.Y", "title": "Other specified disorders of muscles" } ]
=== ICD-11 CODES FOUND === [CB2Z] Pleural, diaphragm or mediastinal disorders, unspecified Also known as: Pleural, diaphragm or mediastinal disorders, unspecified [LA76] Structural developmental anomalies of pleura Definition: Anomalies of the lining of the lung (visceral pleura) and thoracic cavity (parietal pleura) Also known as: Structural developmental anomalies of pleura | Malformations of pleura | anomaly of pleura | abnormal pleura | pleural anomaly [MD31] Pleurisy Definition: Pleurisy or Pleuritis is the medical term for inflammation of the pleura. The most common cause of pleuritis is infection, but it can also be caused by lupus, rheumatoid arthritis, and certain medicines. Pleurisy or pleuritis usually accumulates exudative pleural effusions. Also known as: Pleurisy | pleuritis | pleurisy NOS | double pleurisy | pleurisy without effusion Excludes: pleurisy with effusion [NB32.60] Laceration of pleura Also known as: Laceration of pleura [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 [GB90.Y] Other specified disorders of kidney or ureter Also known as: Other specified disorders of kidney or ureter | Other secondary disorders of kidney or ureter | Other disorders of kidney and ureter NEC | Inflammatory diseases of the renal pelvis or the ureter without tubulo-interstitial nephritis | Infectious diseases of the renal pelvis or the ureter without tubulo-interstitial nephritis [DB9Z] Diseases of liver, unspecified Also known as: Diseases of liver, unspecified | liver disease | liver condition NOS | organ liver disease | hepatopathy [9A78.2Z] Corneal oedema, unspecified Also known as: Corneal oedema, unspecified | Corneal oedema | infiltrate of cornea [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 === GRAPH WALKS === --- Walk 1 --- [CB2Z] Pleural, diaphragm or mediastinal disorders, unspecified --PARENT--> [?] Pleural, diaphragm or mediastinal disorders Def: Pleural, diaphragm and mediastinal disorders are disorders of the potential space between the two pleura (visceral and parietal) of the lungs, disorders of the diaphragm and mediastinum. The mediastin... --CHILD--> [CB20] Pleural plaque Def: Deposits of hyalinized collagen fibres in the parietal pleura that result from chronic inflammation. Most commonly associated with past exposure to asbestos, typically becoming visible years after inh... --- Walk 2 --- [CB2Z] Pleural, diaphragm or mediastinal disorders, unspecified --PARENT--> [?] Pleural, diaphragm or mediastinal disorders Def: Pleural, diaphragm and mediastinal disorders are disorders of the potential space between the two pleura (visceral and parietal) of the lungs, disorders of the diaphragm and mediastinum. The mediastin... --CHILD--> [CB21] Pneumothorax Def: Pneumothorax is an abnormal collection of air or gas in the pleural space that separates the lung from the chest wall, and that may interfere with normal breathing.... --- Walk 3 --- [LA76] Structural developmental anomalies of pleura Def: Anomalies of the lining of the lung (visceral pleura) and thoracic cavity (parietal pleura)... --PARENT--> [?] Structural developmental anomalies of the respiratory system --CHILD--> [LA72] Laryngotracheooesophageal cleft Def: A laryngo-tracheo-oesophageal cleft (LC) is a congenital malformation characterised by an abnormal, posterior, sagittal communication between the larynx and the pharynx, possibly extending downward be... --- Walk 4 --- [LA76] Structural developmental anomalies of pleura Def: Anomalies of the lining of the lung (visceral pleura) and thoracic cavity (parietal pleura)... --PARENT--> [?] Structural developmental anomalies of the respiratory system --CHILD--> [LA70] Structural developmental anomalies of the nose or cavum Def: Any condition caused by failure of the nose and cavum to correctly develop during the antenatal period.... --- Walk 5 --- [MD31] Pleurisy Def: Pleurisy or Pleuritis is the medical term for inflammation of the pleura. The most common cause of pleuritis is infection, but it can also be caused by lupus, rheumatoid arthritis, and certain medicin... --EXCLUDES--> [?] Pleural effusion Def: Presence of fluid in the pleural cavity resulting from excessive transudation or exudation from the pleural surfaces.... --CHILD--> [?] Pneumococcal pleurisy --- Walk 6 --- [MD31] Pleurisy Def: Pleurisy or Pleuritis is the medical term for inflammation of the pleura. The most common cause of pleuritis is infection, but it can also be caused by lupus, rheumatoid arthritis, and certain medicin... --EXCLUDES--> [?] Pleural effusion Def: Presence of fluid in the pleural cavity resulting from excessive transudation or exudation from the pleural surfaces.... --EXCLUDES--> [?] Pleurisy Def: Pleurisy or Pleuritis is the medical term for inflammation of the pleura. The most common cause of pleuritis is infection, but it can also be caused by lupus, rheumatoid arthritis, and certain medicin...
[ "[CB2Z] Pleural, diaphragm or mediastinal disorders, unspecified\n --PARENT--> [?] Pleural, diaphragm or mediastinal disorders\n Def: Pleural, diaphragm and mediastinal disorders are disorders of the potential space between the two pleura (visceral and parietal) of the lungs, disorders of the diaphragm and mediastinum. The mediastin...\n --CHILD--> [CB20] Pleural plaque\n Def: Deposits of hyalinized collagen fibres in the parietal pleura that result from chronic inflammation. Most commonly associated with past exposure to asbestos, typically becoming visible years after inh...", "[CB2Z] Pleural, diaphragm or mediastinal disorders, unspecified\n --PARENT--> [?] Pleural, diaphragm or mediastinal disorders\n Def: Pleural, diaphragm and mediastinal disorders are disorders of the potential space between the two pleura (visceral and parietal) of the lungs, disorders of the diaphragm and mediastinum. The mediastin...\n --CHILD--> [CB21] Pneumothorax\n Def: Pneumothorax is an abnormal collection of air or gas in the pleural space that separates the lung from the chest wall, and that may interfere with normal breathing....", "[LA76] Structural developmental anomalies of pleura\n Def: Anomalies of the lining of the lung (visceral pleura) and thoracic cavity (parietal pleura)...\n --PARENT--> [?] Structural developmental anomalies of the respiratory system\n --CHILD--> [LA72] Laryngotracheooesophageal cleft\n Def: A laryngo-tracheo-oesophageal cleft (LC) is a congenital malformation characterised by an abnormal, posterior, sagittal communication between the larynx and the pharynx, possibly extending downward be...", "[LA76] Structural developmental anomalies of pleura\n Def: Anomalies of the lining of the lung (visceral pleura) and thoracic cavity (parietal pleura)...\n --PARENT--> [?] Structural developmental anomalies of the respiratory system\n --CHILD--> [LA70] Structural developmental anomalies of the nose or cavum\n Def: Any condition caused by failure of the nose and cavum to correctly develop during the antenatal period....", "[MD31] Pleurisy\n Def: Pleurisy or Pleuritis is the medical term for inflammation of the pleura. The most common cause of pleuritis is infection, but it can also be caused by lupus, rheumatoid arthritis, and certain medicin...\n --EXCLUDES--> [?] Pleural effusion\n Def: Presence of fluid in the pleural cavity resulting from excessive transudation or exudation from the pleural surfaces....\n --CHILD--> [?] Pneumococcal pleurisy", "[MD31] Pleurisy\n Def: Pleurisy or Pleuritis is the medical term for inflammation of the pleura. The most common cause of pleuritis is infection, but it can also be caused by lupus, rheumatoid arthritis, and certain medicin...\n --EXCLUDES--> [?] Pleural effusion\n Def: Presence of fluid in the pleural cavity resulting from excessive transudation or exudation from the pleural surfaces....\n --EXCLUDES--> [?] Pleurisy\n Def: Pleurisy or Pleuritis is the medical term for inflammation of the pleura. The most common cause of pleuritis is infection, but it can also be caused by lupus, rheumatoid arthritis, and certain medicin..." ]
CB2Z
Pleural, diaphragm or mediastinal disorders, unspecified
[ { "from_icd11": "CB2Z", "icd10_code": "J948", "icd10_title": "Other specified pleural conditions" }, { "from_icd11": "CB2Z", "icd10_code": "J949", "icd10_title": "Pleural condition, unspecified" }, { "from_icd11": "CB2Z", "icd10_code": "J90-J94", "icd10_title": "" }, { "from_icd11": "CB2Z", "icd10_code": "J94", "icd10_title": "Other pleural conditions" }, { "from_icd11": "LA76", "icd10_code": "Q340", "icd10_title": "Anomaly of pleura" }, { "from_icd11": "MD31", "icd10_code": "R091", "icd10_title": "Pleurisy" }, { "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": "DB9Z", "icd10_code": "K7681", "icd10_title": "Hepatopulmonary syndrome" }, { "from_icd11": "DB9Z", "icd10_code": "K7689", "icd10_title": "Other specified diseases of liver" }, { "from_icd11": "DB9Z", "icd10_code": "K769", "icd10_title": "Liver disease, unspecified" }, { "from_icd11": "DB9Z", "icd10_code": "K77", "icd10_title": "Liver disorders in diseases classified elsewhere" }, { "from_icd11": "DB9Z", "icd10_code": "K762", "icd10_title": "Central hemorrhagic necrosis of liver" }, { "from_icd11": "DB9Z", "icd10_code": "K70-K77", "icd10_title": "" }, { "from_icd11": "DB9Z", "icd10_code": "K778", "icd10_title": "" } ]
J948
Other specified pleural conditions
Subject 2A was a normally developing male until 18 months of age, with multiple single words and the ability to recite the alphabet (by parental report) before losing all speech and developing repetitive self stimulating behaviours. He underwent a brain MRI, head computed tomography (CT) and EEG at 4 years of age which were reportedly normal. Seizures, self injurious behaviours, auditory and visual deficits were absent. Initial evaluation for ASD was performed at age 3 years . Subject 2A demonstrated a complete lack of speech, poor eye contact, and tried to remain distant in physical proximity from the clinician. He did not mimic any action or comply with any overt requests. Parents reported (on PDD checklist and in parent interview) an inability to socialise with peers or understand the emotions of others, lack of reaction to events (happy or sad), a fixation with ears and toes, lack of a sense of danger, flapped hands (particularly when excited) and extreme sensitivity to loud noises. At the time of evaluation for this study, the subject had regained some use of single words and short phrases. On physical examination (this study), his height, weight and head circumference were at the 25th, 5th and 75th centile, respectively. No significant dysmorphology was identified aside from a short philtrum, narrow hands and mild ligamentous laxity. He is the only sibling to have an early regressive course.
3.853516
0.966797
sec[1]/sec[0]/p[2]
en
0.999995
18349135
https://doi.org/10.1136/jmg.2008.057505
[ "subject", "lack", "developing", "single", "words", "speech", "self", "behaviours", "head", "physical" ]
[ { "code": "9D5Z", "title": "Subjective visual experiences, unspecified" }, { "code": "9D5Y", "title": "Other specified subjective visual experiences" }, { "code": "AB32.0", "title": "Persistent Postural-Perceptual Dizziness" }, { "code": "MC41", "title": "Tinnitus" }, { "code": "PC50.Z", "title": "Intentional self-harm by being struck by projectile from firearm, unspecified" }, { "code": "MG44.1Z", "title": "Lack of expected normal physiological development, unspecified" }, { "code": "QD71.0", "title": "Homelessness" }, { "code": "MB21.1Z", "title": "Amnesia, unspecified" }, { "code": "MG43.7", "title": "Anorexia" }, { "code": "QF2A", "title": "Difficulty or need for assistance with community participation" } ]
=== ICD-11 CODES FOUND === [9D5Z] Subjective visual experiences, unspecified Also known as: Subjective visual experiences, unspecified [9D5Y] Other specified subjective visual experiences Also known as: Other specified subjective visual experiences | Sudden visual loss | sudden loss of vision | Chromatopsia | Metamorphopsia Includes: Sudden visual loss [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 [MC41] Tinnitus Definition: A nonspecific symptom of hearing disorder characterised by the sensation of buzzing, ringing, clicking, pulsations, and other noises in the ear in the absence of appropriate corresponding external stimuli and in the absence of what the examiner can hear with a stethoscope. Also known as: Tinnitus | noises in ear | observation of tinnitus | ringing in ear | tinnitus aurium [PC50.Z] Intentional self-harm by being struck by projectile from firearm, unspecified Also known as: Intentional self-harm by being struck by projectile from firearm, unspecified | Intentional self-harm by being struck by projectile from firearm | shot self | subject shot self | decedent shot himself [MG44.1Z] Lack of expected normal physiological development, unspecified Also known as: Lack of expected normal physiological development, unspecified | Lack of expected normal physiological development | delayed physiological development | unspecified delay in development | development arrest [QD71.0] Homelessness Also known as: Homelessness | lack of housing | hobo | problem of homelessness | lack of shelter [MB21.1Z] Amnesia, unspecified Also known as: Amnesia, unspecified | Amnesia | disturbance of memory | lack of memory | loss of memory [MG43.7] Anorexia Definition: Anorexia is a pathological lack or loss of appetite. Also known as: Anorexia | anorectic | anorexic | lack of appetite | Loss of appetite Includes: Loss of appetite Excludes: loss of appetite of nonorganic origin | anorexia nervosa | Decreased appetite [QF2A] Difficulty or need for assistance with community participation Also known as: Difficulty or need for assistance with community participation | difficulty with community participation | need for assistance with community participation | need for assistance with community, social and civic life | difficulty with community, social and civic life Includes: Lack of relaxation or leisure === GRAPH WALKS === --- Walk 1 --- [9D5Z] Subjective visual experiences, unspecified --PARENT--> [?] Subjective visual experiences Def: Subjective Visual Experiences are experiences reported by patients, whose presence or absence cannot be verified objectively.... --CHILD--> [9D51] Transient visual loss --- Walk 2 --- [9D5Z] Subjective visual experiences, unspecified --PARENT--> [?] Subjective visual experiences Def: Subjective Visual Experiences are experiences reported by patients, whose presence or absence cannot be verified objectively.... --CHILD--> [9D51] Transient visual loss --- Walk 3 --- [9D5Y] Other specified subjective visual experiences --PARENT--> [?] Subjective visual experiences Def: Subjective Visual Experiences are experiences reported by patients, whose presence or absence cannot be verified objectively.... --CHILD--> [9D52] Hemifield losses --- Walk 4 --- [9D5Y] Other specified subjective visual experiences --PARENT--> [?] Subjective visual experiences Def: Subjective Visual Experiences are experiences reported by patients, whose presence or absence cannot be verified objectively.... --CHILD--> [9D50] Visual discomfort --- Walk 5 --- [AB32.0] Persistent Postural-Perceptual Dizziness Def: 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 ma... --PARENT--> [AB32] Chronic vestibular syndrome Def: A clinical syndrome of chronic vertigo, dizziness, or unsteadiness lasting months to years and generally including features suggestive of persistent vestibular system dysfunction (e.g., oscillopsia, n... --PARENT--> [?] Diseases of inner ear --- Walk 6 --- [AB32.0] Persistent Postural-Perceptual Dizziness Def: 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 ma... --PARENT--> [AB32] Chronic vestibular syndrome Def: A clinical syndrome of chronic vertigo, dizziness, or unsteadiness lasting months to years and generally including features suggestive of persistent vestibular system dysfunction (e.g., oscillopsia, n... --CHILD--> [AB32.0] Persistent Postural-Perceptual Dizziness Def: 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 ma...
[ "[9D5Z] Subjective visual experiences, unspecified\n --PARENT--> [?] Subjective visual experiences\n Def: Subjective Visual Experiences are experiences reported by patients, whose presence or absence cannot be verified objectively....\n --CHILD--> [9D51] Transient visual loss", "[9D5Z] Subjective visual experiences, unspecified\n --PARENT--> [?] Subjective visual experiences\n Def: Subjective Visual Experiences are experiences reported by patients, whose presence or absence cannot be verified objectively....\n --CHILD--> [9D51] Transient visual loss", "[9D5Y] Other specified subjective visual experiences\n --PARENT--> [?] Subjective visual experiences\n Def: Subjective Visual Experiences are experiences reported by patients, whose presence or absence cannot be verified objectively....\n --CHILD--> [9D52] Hemifield losses", "[9D5Y] Other specified subjective visual experiences\n --PARENT--> [?] Subjective visual experiences\n Def: Subjective Visual Experiences are experiences reported by patients, whose presence or absence cannot be verified objectively....\n --CHILD--> [9D50] Visual discomfort", "[AB32.0] Persistent Postural-Perceptual Dizziness\n Def: 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 ma...\n --PARENT--> [AB32] Chronic vestibular syndrome\n Def: A clinical syndrome of chronic vertigo, dizziness, or unsteadiness lasting months to years and generally including features suggestive of persistent vestibular system dysfunction (e.g., oscillopsia, n...\n --PARENT--> [?] Diseases of inner ear", "[AB32.0] Persistent Postural-Perceptual Dizziness\n Def: 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 ma...\n --PARENT--> [AB32] Chronic vestibular syndrome\n Def: A clinical syndrome of chronic vertigo, dizziness, or unsteadiness lasting months to years and generally including features suggestive of persistent vestibular system dysfunction (e.g., oscillopsia, n...\n --CHILD--> [AB32.0] Persistent Postural-Perceptual Dizziness\n Def: 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 ma..." ]
9D5Z
Subjective visual experiences, unspecified
[ { "from_icd11": "9D5Z", "icd10_code": "H53143", "icd10_title": "Visual discomfort, bilateral" }, { "from_icd11": "9D5Z", "icd10_code": "H53141", "icd10_title": "Visual discomfort, right eye" }, { "from_icd11": "9D5Z", "icd10_code": "H53149", "icd10_title": "Visual discomfort, unspecified" }, { "from_icd11": "9D5Z", "icd10_code": "H53121", "icd10_title": "Transient visual loss, right eye" }, { "from_icd11": "9D5Z", "icd10_code": "H53122", "icd10_title": "Transient visual loss, left eye" }, { "from_icd11": "9D5Z", "icd10_code": "H5315", "icd10_title": "Visual distortions of shape and size" }, { "from_icd11": "9D5Z", "icd10_code": "H53132", "icd10_title": "Sudden visual loss, left eye" }, { "from_icd11": "9D5Z", "icd10_code": "H53123", "icd10_title": "Transient visual loss, bilateral" }, { "from_icd11": "9D5Z", "icd10_code": "H53129", "icd10_title": "Transient visual loss, unspecified eye" }, { "from_icd11": "9D5Z", "icd10_code": "H5319", "icd10_title": "Other subjective visual disturbances" }, { "from_icd11": "9D5Z", "icd10_code": "H5316", "icd10_title": "Psychophysical visual disturbances" }, { "from_icd11": "9D5Z", "icd10_code": "H53142", "icd10_title": "Visual discomfort, left eye" }, { "from_icd11": "9D5Z", "icd10_code": "H53131", "icd10_title": "Sudden visual loss, right eye" }, { "from_icd11": "9D5Z", "icd10_code": "H53133", "icd10_title": "Sudden visual loss, bilateral" }, { "from_icd11": "9D5Z", "icd10_code": "H5310", "icd10_title": "Unspecified subjective visual disturbances" } ]
H53143
Visual discomfort, bilateral
A 35‐year‐old female was diagnosed with chronic ‘favourable’ ATL at 12 weeks’ gestation following a routine blood count. Her FBC revealed: WCC 17.2 × 10 9 /L (normal range: 5.6‐16.9 × 10 9 /L), normal haemoglobin and platelets, corrected calcium and LDH. Her blood film showed >5% abnormal pleomorphic lymphocytes with positive HTLV‐1 serology. Diagnostic Immunophenotyping showed CD3+CD4+CD25‐CD7‐ population and HTLV‐1 PVL 45%. She was commenced on ZDV 250 mg twice daily and subcutaneous pegylated IFN‐α‐2b pegasys 1.5 mcg/kg weekly at the start of the second trimester. Raltegravir 400 mg twice daily was added at 32 weeks. There was not a significant response to therapy despite escalating doses of ZDV to 500 mg twice daily and IFN‐α 6mcg/kg, and so an elective caesarean was expedited at 38 weeks’ gestation. The infant was formula‐fed and completed 6 weeks oral ZDV syrup. At delivery neonatal HTLV PVL was undetectable and remained undetectable at 6 weeks and 3 months. The baby remains well and is under active follow‐up with repeat testing planned at 18 months. Following delivery, the mother was treated with mogamulizumab 1 mg/kg due to lack of response to ZDV/IFN‐ α. Following one dose, haematological remission was achieved, and PVL was reduced to 0.06%. She has received a total of three doses, currently stopped due to mild skin rash and remains in a persistent haematological remission 8 months later.
4.054688
0.974609
sec[0]/sec[3]/p[0]
en
0.999997
PMC9175930
https://doi.org/10.1002/jha2.142
[ "htlv", "twice", "daily", "gestation", "blood", "response", "doses", "delivery", "undetectable", "remains" ]
[ { "code": "QD0Y&XN1WJ", "title": "Carrier of human T-lymphotropic virus type- 1 infection" }, { "code": "8A45.00", "title": "Human T-cell lymphotropic virus-associated myelopathy" }, { "code": "EA88.00", "title": "Human T-cell lymphotropic virus type 1 associated infective dermatitis of childhood" }, { "code": "2A90.5", "title": "Adult T-cell lymphoma or leukaemia, human T-cell lymphotropic virus type 1-associated" }, { "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": "JA61.Y", "title": "Other specified venous complications in pregnancy" }, { "code": "JA8E", "title": "Maternal care related to prolonged pregnancy" }, { "code": "JA01.Y", "title": "Other specified ectopic pregnancy" } ]
=== ICD-11 CODES FOUND === [8A45.00] Human T-cell lymphotropic virus-associated myelopathy Definition: Human T-cell lymphotropic virus (HTLV) is a retrovirus and causes immune mediated diseases of the nervous system. Human T-cell lymphotropic virus type 1 (HTLV-1) and Human T-cell lymphotropic virus type 2 (HTLV-2) are closely related retroviruses with similar biological properties and common modes of transport. Also known as: Human T-cell lymphotropic virus-associated myelopathy | tropical spastic paraplegia | HTLV- [human T-cell lymphotropic virus]-associated myelopathy | Tropical spastic paraparesis [EA88.00] Human T-cell lymphotropic virus type 1 associated infective dermatitis of childhood Definition: An inflammatory dermatitis of childhood which develops in a minority of children with HTLV‐1 infection, acquired usually via breast milk from an infected mother. Although the disease may clear spontaneously in adolescence, there is a high risk of development of Human T-cell lymphotropic virus-associated myelopathy (tropical spastic paraparesis) in later life. The onset is most frequent between the ages of 2 and 3, but it can manifest from as early as a few months of age to late childhood. Sites Also known as: Human T-cell lymphotropic virus type 1 associated infective dermatitis of childhood | HTLV‐1 associated infective dermatitis of childhood | Human T-lymphotropic virus type 1 associated infective dermatitis of childhood [2A90.5] Adult T-cell lymphoma or leukaemia, human T-cell lymphotropic virus type 1-associated Definition: A peripheral (mature) T-cell neoplasm linked to the human T-cell leukaemia virus type 1 (HTLV-1). Adult T-cell leukaemia/lymphoma is endemic in several regions of the world, in particular Japan, the Caribbean, and parts of Central Africa. Also known as: Adult T-cell lymphoma or leukaemia, human T-cell lymphotropic virus type 1-associated | adult t-cell lymphoma | adult t cell leukaemia lymphoma | adult t-cell leukaemia | cortical T ALL [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 [JA61.Y] Other specified venous complications in pregnancy Also known as: Other specified venous complications in pregnancy | Venous thrombosis in pregnancy | antepartum thrombosis NOS | Gestational thrombosis NOS | thrombosis in pregnancy NOS [JA8E] Maternal care related to prolonged pregnancy Definition: Pregnancy that has exceeded a duration of 42 weeks from the last menstrual period. Also known as: Maternal care related to prolonged pregnancy | post-term pregnancy | pregnancy beyond 42 weeks of gestation | prolonged gestation | postmature pregnancy Includes: Post-term [JA01.Y] Other specified ectopic pregnancy Also known as: Other specified ectopic pregnancy | Cornual gestation or pregnancy | cornual gestation | cornual pregnancy | Cervical pregnancy === GRAPH WALKS === --- Walk 1 --- [8A45.00] Human T-cell lymphotropic virus-associated myelopathy Def: Human T-cell lymphotropic virus (HTLV) is a retrovirus and causes immune mediated diseases of the nervous system. Human T-cell lymphotropic virus type 1 (HTLV-1) and Human T-cell lymphotropic virus ty... --PARENT--> [8A45.0] White matter disorders due to infections --RELATED_TO--> [?] Tabes dorsalis Def: This is a slow degeneration (specifically, demyelination) of the sensory neurons that carry afferent information. The degenerating nerves are in the dorsal columns (posterior columns) of the spinal co... --- Walk 2 --- [8A45.00] Human T-cell lymphotropic virus-associated myelopathy Def: Human T-cell lymphotropic virus (HTLV) is a retrovirus and causes immune mediated diseases of the nervous system. Human T-cell lymphotropic virus type 1 (HTLV-1) and Human T-cell lymphotropic virus ty... --RELATED_TO--> [?] Myelitis due to Human T-lymphotropic virus type 1 Def: An inflammatory disorder of the spinal cord due to infection by the HTLV-1 virus. The symptoms and signs are usually subacute or chronic in onset, and include paraparesis or paraplegia, mild periphera... --PARENT--> [?] Human T-cell lymphotropic virus-associated myelopathy Def: Human T-cell lymphotropic virus (HTLV) is a retrovirus and causes immune mediated diseases of the nervous system. Human T-cell lymphotropic virus type 1 (HTLV-1) and Human T-cell lymphotropic virus ty... --- Walk 3 --- [EA88.00] Human T-cell lymphotropic virus type 1 associated infective dermatitis of childhood Def: An inflammatory dermatitis of childhood which develops in a minority of children with HTLV‐1 infection, acquired usually via breast milk from an infected mother. Although the disease may clear spontan... --PARENT--> [EA88.0] Infectious dermatitis Def: Infective dermatitis (infective eczematoid dermatitis) is an acute exudative dermatitis developing on normal skin surrounding a focus of suppurative infection. Such foci include infected wounds, suppu... --CHILD--> [EA88.0Y] Other specified infectious dermatitis --- Walk 4 --- [EA88.00] Human T-cell lymphotropic virus type 1 associated infective dermatitis of childhood Def: An inflammatory dermatitis of childhood which develops in a minority of children with HTLV‐1 infection, acquired usually via breast milk from an infected mother. Although the disease may clear spontan... --PARENT--> [EA88.0] Infectious dermatitis Def: Infective dermatitis (infective eczematoid dermatitis) is an acute exudative dermatitis developing on normal skin surrounding a focus of suppurative infection. Such foci include infected wounds, suppu... --CHILD--> [EA88.0Z] Infectious dermatitis, unspecified --- Walk 5 --- [2A90.5] Adult T-cell lymphoma or leukaemia, human T-cell lymphotropic virus type 1-associated Def: A peripheral (mature) T-cell neoplasm linked to the human T-cell leukaemia virus type 1 (HTLV-1). Adult T-cell leukaemia/lymphoma is endemic in several regions of the world, in particular Japan, the C... --RELATED_TO--> [?] Adult T-cell leukaemia or lymphoma, skin Def: Adult T cell leukaemia / lymphoma (ATLL) is a malignancy of mature CD4+/ CD25+ T cells caused by the human T-cell leukaemia virus type I (HTLV-1). The primary cutaneous tumoural type tends to show a f... --PARENT--> [?] Mature T-cell or NK-cell lymphomas and lymphoproliferative disorders, primary cutaneous specified types Def: Primary cutaneous T-cell lymphomas (CTCL) and NK-cell lymphomas are malignant lymphoproliferative diseases of unknown cause that are thought to originate from T-lymphocytes in the lymphoid tissue of t... --- Walk 6 --- [2A90.5] Adult T-cell lymphoma or leukaemia, human T-cell lymphotropic virus type 1-associated Def: A peripheral (mature) T-cell neoplasm linked to the human T-cell leukaemia virus type 1 (HTLV-1). Adult T-cell leukaemia/lymphoma is endemic in several regions of the world, in particular Japan, the C... --RELATED_TO--> [?] Adult T-cell leukaemia or lymphoma, skin Def: Adult T cell leukaemia / lymphoma (ATLL) is a malignancy of mature CD4+/ CD25+ T cells caused by the human T-cell leukaemia virus type I (HTLV-1). The primary cutaneous tumoural type tends to show a f... --PARENT--> [?] Mature T-cell or NK-cell lymphomas and lymphoproliferative disorders, primary cutaneous specified types Def: Primary cutaneous T-cell lymphomas (CTCL) and NK-cell lymphomas are malignant lymphoproliferative diseases of unknown cause that are thought to originate from T-lymphocytes in the lymphoid tissue of t...
[ "[8A45.00] Human T-cell lymphotropic virus-associated myelopathy\n Def: Human T-cell lymphotropic virus (HTLV) is a retrovirus and causes immune mediated diseases of the nervous system. Human T-cell lymphotropic virus type 1 (HTLV-1) and Human T-cell lymphotropic virus ty...\n --PARENT--> [8A45.0] White matter disorders due to infections\n --RELATED_TO--> [?] Tabes dorsalis\n Def: This is a slow degeneration (specifically, demyelination) of the sensory neurons that carry afferent information. The degenerating nerves are in the dorsal columns (posterior columns) of the spinal co...", "[8A45.00] Human T-cell lymphotropic virus-associated myelopathy\n Def: Human T-cell lymphotropic virus (HTLV) is a retrovirus and causes immune mediated diseases of the nervous system. Human T-cell lymphotropic virus type 1 (HTLV-1) and Human T-cell lymphotropic virus ty...\n --RELATED_TO--> [?] Myelitis due to Human T-lymphotropic virus type 1\n Def: An inflammatory disorder of the spinal cord due to infection by the HTLV-1 virus. The symptoms and signs are usually subacute or chronic in onset, and include paraparesis or paraplegia, mild periphera...\n --PARENT--> [?] Human T-cell lymphotropic virus-associated myelopathy\n Def: Human T-cell lymphotropic virus (HTLV) is a retrovirus and causes immune mediated diseases of the nervous system. Human T-cell lymphotropic virus type 1 (HTLV-1) and Human T-cell lymphotropic virus ty...", "[EA88.00] Human T-cell lymphotropic virus type 1 associated infective dermatitis of childhood\n Def: An inflammatory dermatitis of childhood which develops in a minority of children with HTLV‐1 infection, acquired usually via breast milk from an infected mother. Although the disease may clear spontan...\n --PARENT--> [EA88.0] Infectious dermatitis\n Def: Infective dermatitis (infective eczematoid dermatitis) is an acute exudative dermatitis developing on normal skin surrounding a focus of suppurative infection. Such foci include infected wounds, suppu...\n --CHILD--> [EA88.0Y] Other specified infectious dermatitis", "[EA88.00] Human T-cell lymphotropic virus type 1 associated infective dermatitis of childhood\n Def: An inflammatory dermatitis of childhood which develops in a minority of children with HTLV‐1 infection, acquired usually via breast milk from an infected mother. Although the disease may clear spontan...\n --PARENT--> [EA88.0] Infectious dermatitis\n Def: Infective dermatitis (infective eczematoid dermatitis) is an acute exudative dermatitis developing on normal skin surrounding a focus of suppurative infection. Such foci include infected wounds, suppu...\n --CHILD--> [EA88.0Z] Infectious dermatitis, unspecified", "[2A90.5] Adult T-cell lymphoma or leukaemia, human T-cell lymphotropic virus type 1-associated\n Def: A peripheral (mature) T-cell neoplasm linked to the human T-cell leukaemia virus type 1 (HTLV-1). Adult T-cell leukaemia/lymphoma is endemic in several regions of the world, in particular Japan, the C...\n --RELATED_TO--> [?] Adult T-cell leukaemia or lymphoma, skin\n Def: Adult T cell leukaemia / lymphoma (ATLL) is a malignancy of mature CD4+/ CD25+ T cells caused by the human T-cell leukaemia virus type I (HTLV-1). The primary cutaneous tumoural type tends to show a f...\n --PARENT--> [?] Mature T-cell or NK-cell lymphomas and lymphoproliferative disorders, primary cutaneous specified types\n Def: Primary cutaneous T-cell lymphomas (CTCL) and NK-cell lymphomas are malignant lymphoproliferative diseases of unknown cause that are thought to originate from T-lymphocytes in the lymphoid tissue of t...", "[2A90.5] Adult T-cell lymphoma or leukaemia, human T-cell lymphotropic virus type 1-associated\n Def: A peripheral (mature) T-cell neoplasm linked to the human T-cell leukaemia virus type 1 (HTLV-1). Adult T-cell leukaemia/lymphoma is endemic in several regions of the world, in particular Japan, the C...\n --RELATED_TO--> [?] Adult T-cell leukaemia or lymphoma, skin\n Def: Adult T cell leukaemia / lymphoma (ATLL) is a malignancy of mature CD4+/ CD25+ T cells caused by the human T-cell leukaemia virus type I (HTLV-1). The primary cutaneous tumoural type tends to show a f...\n --PARENT--> [?] Mature T-cell or NK-cell lymphomas and lymphoproliferative disorders, primary cutaneous specified types\n Def: Primary cutaneous T-cell lymphomas (CTCL) and NK-cell lymphomas are malignant lymphoproliferative diseases of unknown cause that are thought to originate from T-lymphocytes in the lymphoid tissue of t..." ]
QD0Y&XN1WJ
Carrier of human T-lymphotropic virus type- 1 infection
[ { "from_icd11": "8A45.00", "icd10_code": "G041", "icd10_title": "Tropical spastic paraplegia" }, { "from_icd11": "2A90.5", "icd10_code": "C9151", "icd10_title": "Adult T-cell lymphoma/leukemia (HTLV-1-associated), in remission" }, { "from_icd11": "2A90.5", "icd10_code": "C9150", "icd10_title": "Adult T-cell lymphoma/leukemia (HTLV-1-associated) not having achieved remission" }, { "from_icd11": "2A90.5", "icd10_code": "C9152", "icd10_title": "Adult T-cell lymphoma/leukemia (HTLV-1-associated), in relapse" }, { "from_icd11": "2A90.5", "icd10_code": "C915", "icd10_title": "Adult T-cell lymphoma/leukemia (HTLV-1-associated)" }, { "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": "JA8E", "icd10_code": "O480", "icd10_title": "Post-term pregnancy" } ]
G041
Tropical spastic paraplegia
In February 2005, at age 36, the patient developed a painful fistula-associated rectal abscess. At this time, the patient's ongoing symptoms included chronic bone and abdominal pain, swollen joints, and debilitating fatigue. On February 18th, she was placed on cephalexin to treat the abscess previous to a scheduled surgery to correct the fistula. Following a week with no improvement in abscess pain while on the antibiotic, the patient then developed an influenza-like infection (high fevers, chills, headache, cough, and rhinorrhea). After the first onset of fever, the abscess pain was no longer apparent. The recurrent fevers (103-104°F) from the infection persisted for four days and were associated with a complete disappearance of all other disease symptoms. This was followed by an increase in appetite and weight. On March 18th, the patient underwent the scheduled surgery to correct the fistula. Her energy level had been continually improving and after a month she was running up to 3 miles a day and was able to run up hills that she could not even walk up prior to her remission. After approximately 10 weeks of this symptom-free remission, her previous disease symptoms began to return. The initial symptoms included hugely swollen knees and diarrhea. The patient was again placed on cephalexin in the expectation that it might result in another remission, but the intervention had no effect on symptoms.
3.664063
0.985352
sec[1]/p[3]
en
0.999996
21592411
https://doi.org/10.1186/1471-230X-11-57
[ "abscess", "fistula", "this", "pain", "remission", "february", "associated", "included", "swollen", "cephalexin" ]
[ { "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": "FA37.Y", "title": "Other specified certain joint disorders, not elsewhere classified" }, { "code": "GC04.Z", "title": "Fistula of the genitourinary tract, unspecified" }, { "code": "CA0A.Z", "title": "Chronic rhinosinusitis, unspecified" }, { "code": "LA8C.2", "title": "Congenital coronary arterial fistula" }, { "code": "CA44", "title": "Pyothorax" } ]
=== 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 [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 [GC04.Z] Fistula of the genitourinary tract, unspecified Also known as: Fistula of the genitourinary tract, unspecified | Fistula of the genitourinary tract | persistent urinary fistula | persistent urinary tract fistula | recurrent urinary fistula [CA0A.Z] Chronic rhinosinusitis, unspecified Also known as: Chronic rhinosinusitis, unspecified | Chronic rhinosinusitis | Chronic sinusitis | chronic sinusitis NOS | unspecified sinusitis [LA8C.2] Congenital coronary arterial fistula Definition: A congenital cardiovascular malformation in which a coronary artery communicates, through an anomalous channel, with a cardiac chamber or with any segment of the systemic or pulmonary circulation. Additional information: this communication may be simple and direct or may be tortuous and dilated. In order of frequency the involved coronary artery is the right, the left and, rarely, both coronary arteries. Occasionally multiple fistulas are present. Also known as: Congenital coronary arterial fistula | coronary fistula | congenital arteriovenous coronary fistula | congenital coronary fistula to pulmonary artery | Congenital coronary arterial fistula to right ventricle Includes: congenital coronary fistula to pulmonary artery Excludes: anomalous origin of coronary artery from pulmonary arterial tree [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 === 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--> [?] Epidermoid cyst Def: A cutaneous cyst with an epidermoid wall filled with keratin and its breakdown products. It most commonly forms as the result of squamous metaplasia in a damaged sebaceous gland but may result from tr... --- 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 --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 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--> [FA10.0] Bacterial 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--> [?] Postinfectious arthropathies
[ "[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--> [?] Epidermoid cyst\n Def: A cutaneous cyst with an epidermoid wall filled with keratin and its breakdown products. It most commonly forms as the result of squamous metaplasia in a damaged sebaceous gland but may result from tr...", "[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 --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...", "[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--> [FA10.0] Bacterial 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--> [?] Postinfectious arthropathies" ]
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 patient was operated upon via a left fronto-temporo-parietal craniectomy. Intraoperative a soft purplish, easily separated from dural surface lesion was discovered that was not encapsulated and was originated from the diploe. The overlying skin was normal and the galea was not involved. There was a bleeding tendency, nevertheless the lesion was totally excised and a cranioplasty with bone cement was performed. Histology revealed a highly cellular tumor, composed of monoclonal plasma cells positive for immunoglobin lambda light chain. The diagnosis was plasmacytoma of the skull. Six hours later the patient developed an epidural hematoma that required an immediate evacuation [Figure 2 ]. The patient was admitted to the intensive care unit for four days. After readmission to neurosurgery department her neurological status was gradually improved with an accepted cosmetic appearance of the cranial vault. For further investigation to detect possible multiple myeloma a bone scan was performed that revealed no osteolytic lesions. On laboratory examination there was no evidence of systemic myelomatous changes, cancer or anemia. M component was not detected in serum protein electrophoresis, Bence-Jones protein and excretion of immunoglobin elements was not found in urine. The patient underwent bone marrow aspiration and bronchoscopy which were also negative. Saline cultures revealed active tuberculosis.
3.832031
0.984863
sec[1]/sec[2]/p[0]
en
0.999996
20062671
https://doi.org/10.1186/1757-1626-2-9154
[ "that", "bone", "lesion", "immunoglobin", "protein", "operated", "upon", "fronto", "temporo", "parietal" ]
[ { "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": "FC0Z", "title": "Diseases of the musculoskeletal system or connective tissue, unspecified" }, { "code": "FB84.Z", "title": "Osteomyelitis or osteitis, unspecified" }, { "code": "FB80.Z", "title": "Disorder of bone density or structure, unspecified" }, { "code": "FB86.11", "title": "Hypertrophy of bone" }, { "code": "FB86.1Z", "title": "Bone hyperplasias, unspecified" } ]
=== ICD-11 CODES FOUND === [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 [FC0Z] Diseases of the musculoskeletal system or connective tissue, unspecified Also known as: Diseases of the musculoskeletal system or connective tissue, unspecified | bone disease NOS | bone disorder NOS | bone lesion NOS | musculoskeletal complications NOS [FB84.Z] Osteomyelitis or osteitis, unspecified Also known as: Osteomyelitis or osteitis, unspecified | Osteomyelitis or osteitis | bone inflammation | bone ulcer | bone inflammatory disease [FB80.Z] Disorder of bone density or structure, unspecified Also known as: Disorder of bone density or structure, unspecified | Certain specified disorders of bone density or structure [FB86.11] Hypertrophy of bone Also known as: Hypertrophy of bone | bone thickening | periosteum thickening | Infantile cortical hyperostoses | Post traumatic subperiosteal ossification [FB86.1Z] Bone hyperplasias, unspecified Also known as: Bone hyperplasias, unspecified | Bone hyperplasias === GRAPH WALKS === --- Walk 1 --- [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... --EXCLUDES--> [?] Headache, not elsewhere classified Def: Headache with characteristic features suggesting that it is a unique diagnostic entity, a finding or complaint, but not fulfilling criteria for any of the headache disorders described above.... --- Walk 3 --- [QA76] Medication or substance that is known to be an allergen without injury or harm Def: Medication that has previously been identified as an allergen to the patient is administered, but does not result in injury or harm.... --EXCLUDES--> [?] Medication or substance that is known to be an allergen, as mode of injury or harm --PARENT--> [?] Mode of injury or harm associated with exposure to a drug, medicament or biological substance --- Walk 4 --- [QA76] Medication or substance that is known to be an allergen without injury or harm Def: Medication that has previously been identified as an allergen to the patient is administered, but does not result in injury or harm.... --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--> [PL13.0] Overdose of substance, as mode of injury or harm Def: Incorrect dose - too high... --- 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 --EXCLUDES--> [?] Headache, not elsewhere classified\n Def: Headache with characteristic features suggesting that it is a unique diagnostic entity, a finding or complaint, but not fulfilling criteria for any of the headache disorders described above....", "[QA76] Medication or substance that is known to be an allergen without injury or harm\n Def: Medication that has previously been identified as an allergen to the patient is administered, but does not result in injury or harm....\n --EXCLUDES--> [?] Medication or substance that is known to be an allergen, as mode of injury or harm\n --PARENT--> [?] Mode of injury or harm associated with exposure to a drug, medicament or biological substance", "[QA76] Medication or substance that is known to be an allergen without injury or harm\n Def: Medication that has previously been identified as an allergen to the patient is administered, but does not result in injury or harm....\n --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--> [PL13.0] Overdose of substance, as mode of injury or harm\n Def: Incorrect dose - too high...", "[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
In 2002, fever, vomiting, and irritability developed in a 2-month-old infant, followed 12 hours later by labored breathing and a generalized rash. She was taken to a clinic where she experienced cardiac arrest and underwent cardiopulmonary resuscitation. She was transferred to a nearby emergency room where she died ≈1 hour later. Meningococcemia was suspected and household members were given prescriptions for rifampin. Waterhouse-Friderichsen syndrome was noted on autopsy, and N. meningitidis was isolated from a swab of brain tissue. Three days after the death of the case-patient and 1 day after completing a 2-day course of rifampin, a fever and lethargy developed in the case-patient's 6-year-old sister. Blood cultures were obtained and she was hospitalized, given antimicrobial drug treatment (ceftriaxone), and observed. No cerebrospinal fluid was collected. Blood cultures were subsequently positive for N. meningitidis . She responded to ceftriaxone and continued treatment as an outpatient after a short hospitalization. Household contacts, along with other close contacts of the 6-year-old girl, again received chemoprophylaxis. It was recommended that adults be treated with ciprofloxacin and children be treated with ceftriaxone because of concerns that 1 or both siblings could have had rifampin-resistant meningococcal infections. No additional related cases were identified over the following weeks.
4.03125
0.974121
sec[0]/p[4]
en
0.999996
15963302
https://doi.org/10.3201/eid1106.050143
[ "rifampin", "ceftriaxone", "fever", "household", "meningitidis", "blood", "cultures", "contacts", "that", "treated" ]
[ { "code": "MG50.91", "title": "Third generation cephalosporin resistant Salmonella" }, { "code": "MG50.A2", "title": "Third-generation cephalosporins resistant Shigella" }, { "code": "MG51.12", "title": "Third-generation cephalosporins resistant Streptococcus pneumoniae" }, { "code": "MG50.52", "title": "Third-generation cephalosporin resistant Klebsiella pneumoniae" }, { "code": "MG50.22", "title": "Third generation cephalosporin resistant Escherichia coli" }, { "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" } ]
=== ICD-11 CODES FOUND === [MG50.91] Third generation cephalosporin resistant Salmonella Also known as: Third generation cephalosporin resistant Salmonella | 3GC - [third generation cephalosporin] resistant Salmonella | Cefotaxime resistant Salmonella | Ceftazidime resistant Salmonella | Ceftriaxone-resistant Salmonella [MG50.A2] Third-generation cephalosporins resistant Shigella Also known as: Third-generation cephalosporins resistant Shigella | Cefotaxime resistant Shigella | Ceftazidime resistant Shigella | Ceftriaxone resistant Shigella [MG51.12] Third-generation cephalosporins resistant Streptococcus pneumoniae Also known as: Third-generation cephalosporins resistant Streptococcus pneumoniae | Cefotaxime resistant Streptococcus pneumoniae | Ceftriaxone resistant Streptococcus pneumoniae [MG50.52] Third-generation cephalosporin resistant Klebsiella pneumoniae Also known as: Third-generation cephalosporin resistant Klebsiella pneumoniae | 3GC - [third generation cephalosporin] resistant Klebsiella pneumoniae | Cefotaxime resistant Klebsiella pneumoniae | Ceftazidime resistant Klebsiella pneumoniae | Ceftriaxone-resistant Klebsiella pneumoniae [MG50.22] Third generation cephalosporin resistant Escherichia coli Also known as: Third generation cephalosporin resistant Escherichia coli | 3GC - [third generation cephalosporin] resistant Escherichia coli | Cefotaxime resistant Escherichia coli | Ceftazidime resistant Escherichia coli | Ceftriaxone-resistant Escherichia coli [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 === GRAPH WALKS === --- Walk 1 --- [MG50.91] Third generation cephalosporin resistant Salmonella --PARENT--> [MG50.9] Antibiotic resistant Salmonella --CHILD--> [MG50.92] Carbapenem resistant Salmonella --- Walk 2 --- [MG50.91] Third generation cephalosporin resistant Salmonella --PARENT--> [MG50.9] Antibiotic resistant Salmonella --CHILD--> [MG50.91] Third generation cephalosporin resistant Salmonella --- Walk 3 --- [MG50.A2] Third-generation cephalosporins resistant Shigella --PARENT--> [MG50.A] Antibiotic resistant Shigella --PARENT--> [MG50] Finding of gram negative bacteria resistant to antimicrobial drugs --- Walk 4 --- [MG50.A2] Third-generation cephalosporins resistant Shigella --PARENT--> [MG50.A] Antibiotic resistant Shigella --CHILD--> [MG50.A1] Fluoroquinolone resistant Shigella --- Walk 5 --- [MG51.12] Third-generation cephalosporins resistant Streptococcus pneumoniae --PARENT--> [MG51.1] Antibiotic resistant Streptococcus pneumoniae --CHILD--> [MG51.12] Third-generation cephalosporins resistant Streptococcus pneumoniae --- Walk 6 --- [MG51.12] Third-generation cephalosporins resistant Streptococcus pneumoniae --PARENT--> [MG51.1] Antibiotic resistant Streptococcus pneumoniae --PARENT--> [MG51] Finding of gram positive bacteria resistant to antimicrobial drugs
[ "[MG50.91] Third generation cephalosporin resistant Salmonella\n --PARENT--> [MG50.9] Antibiotic resistant Salmonella\n --CHILD--> [MG50.92] Carbapenem resistant Salmonella", "[MG50.91] Third generation cephalosporin resistant Salmonella\n --PARENT--> [MG50.9] Antibiotic resistant Salmonella\n --CHILD--> [MG50.91] Third generation cephalosporin resistant Salmonella", "[MG50.A2] Third-generation cephalosporins resistant Shigella\n --PARENT--> [MG50.A] Antibiotic resistant Shigella\n --PARENT--> [MG50] Finding of gram negative bacteria resistant to antimicrobial drugs", "[MG50.A2] Third-generation cephalosporins resistant Shigella\n --PARENT--> [MG50.A] Antibiotic resistant Shigella\n --CHILD--> [MG50.A1] Fluoroquinolone resistant Shigella", "[MG51.12] Third-generation cephalosporins resistant Streptococcus pneumoniae\n --PARENT--> [MG51.1] Antibiotic resistant Streptococcus pneumoniae\n --CHILD--> [MG51.12] Third-generation cephalosporins resistant Streptococcus pneumoniae", "[MG51.12] Third-generation cephalosporins resistant Streptococcus pneumoniae\n --PARENT--> [MG51.1] Antibiotic resistant Streptococcus pneumoniae\n --PARENT--> [MG51] Finding of gram positive bacteria resistant to antimicrobial drugs" ]
MG50.91
Third generation cephalosporin resistant Salmonella
[ { "from_icd11": "MG50.91", "icd10_code": "U828", "icd10_title": "" }, { "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" } ]
U828
Multiple strategies are available to treat localized PC including active surveillance, radiotherapy, and surgery . For a patient from the general population, the main deciding factors in selecting treatment modality are cancer control and the potential side effects of the therapeutic procedure with subsequent effects on his quality of life . This decision making process might not be applicable to the transplant candidate diagnosed with screening-detected PC while on the waiting list. Currently, there are no established guidelines addressing management of the disease in pretransplant population. While the 2006 International Society for Heart and Lung Transplantation Guidelines recommend considering HTx in a patient with preceding low-risk PC , some transplant centers require treatment of the disease and documentation of cancer-free interval (i.e., no clinical or biochemical recurrence) before listing the patient as a candidate. The waiting interval before reconsideration for HTx is usually related to oncologic outcomes and estimated risk for PC recurrence. This will pose a special therapeutic dilemma as patient's decisions might be driven by selecting a modality that would offer the shortest waiting for enlistment as a transplant candidate. In this paper we present a case of a patient who was taken off the waiting list due to his clinical diagnosis of biopsy-proven low-risk clinically localized PC.
4.171875
0.92627
sec[0]/p[3]
en
0.999998
23259138
https://doi.org/10.1155/2012/716201
[ "waiting", "this", "transplant", "candidate", "risk", "population", "selecting", "modality", "cancer", "effects" ]
[ { "code": "QB11", "title": "Person awaiting admission to adequate facility elsewhere" }, { "code": "QB12.0", "title": "Organ transplant candidate" }, { "code": "QB12.Z", "title": "Waiting period for investigation or treatment other than awaiting admission to adequate facility elsewhere, unspecified" }, { "code": "QB12.Y", "title": "Other specified waiting period for investigation or treatment other than awaiting admission to adequate facility elsewhere" }, { "code": "4A01.03", "title": "Transient hypogammaglobulinaemia of infancy" }, { "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 === [QB11] Person awaiting admission to adequate facility elsewhere Also known as: Person awaiting admission to adequate facility elsewhere | person on waiting list | unavailability of bed at medical facility | Person awaiting admission to acute hospital | Person awaiting admission to residential aged care service [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 [QB12.Z] Waiting period for investigation or treatment other than awaiting admission to adequate facility elsewhere, unspecified Also known as: Waiting period for investigation or treatment other than awaiting admission to adequate facility elsewhere, unspecified | Waiting period for investigation or treatment other than awaiting admission to adequate facility elsewhere [QB12.Y] Other specified waiting period for investigation or treatment other than awaiting admission to adequate facility elsewhere Also known as: Other specified waiting period for investigation or treatment other than awaiting admission to adequate facility elsewhere | Effective registration for liver transplantation status T1 | Effective registration for liver transplantation status T2 | Effective registration for liver transplantation status T3 | Effective registration for liver transplantation status T4 [4A01.03] Transient hypogammaglobulinaemia of infancy Also known as: Transient hypogammaglobulinaemia of infancy | immunoglobulin maturational delay | THI - [transient hypogammaglobulinaemia of infancy] [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 --- [QB11] Person awaiting admission to adequate facility elsewhere --PARENT--> [?] Factors related to medical facilities or other health care --CHILD--> [QB10] Medical services not available in home --- Walk 2 --- [QB11] Person awaiting admission to adequate facility elsewhere --PARENT--> [?] Factors related to medical facilities or other health care --CHILD--> [QB10] Medical services not available in home --- Walk 3 --- [QB12.0] Organ transplant candidate --PARENT--> [QB12] Waiting period for investigation or treatment other than awaiting admission to adequate facility elsewhere --PARENT--> [?] Factors related to medical facilities or other health care --- Walk 4 --- [QB12.0] Organ transplant candidate --PARENT--> [QB12] Waiting period for investigation or treatment other than awaiting admission to adequate facility elsewhere --CHILD--> [QB12.0] Organ transplant candidate --- Walk 5 --- [QB12.Z] Waiting period for investigation or treatment other than awaiting admission to adequate facility elsewhere, unspecified --PARENT--> [QB12] Waiting period for investigation or treatment other than awaiting admission to adequate facility elsewhere --CHILD--> [QB12.0] Organ transplant candidate --- Walk 6 --- [QB12.Z] Waiting period for investigation or treatment other than awaiting admission to adequate facility elsewhere, unspecified --PARENT--> [QB12] Waiting period for investigation or treatment other than awaiting admission to adequate facility elsewhere --CHILD--> [QB12.0] Organ transplant candidate
[ "[QB11] Person awaiting admission to adequate facility elsewhere\n --PARENT--> [?] Factors related to medical facilities or other health care\n --CHILD--> [QB10] Medical services not available in home", "[QB11] Person awaiting admission to adequate facility elsewhere\n --PARENT--> [?] Factors related to medical facilities or other health care\n --CHILD--> [QB10] Medical services not available in home", "[QB12.0] Organ transplant candidate\n --PARENT--> [QB12] Waiting period for investigation or treatment other than awaiting admission to adequate facility elsewhere\n --PARENT--> [?] Factors related to medical facilities or other health care", "[QB12.0] Organ transplant candidate\n --PARENT--> [QB12] Waiting period for investigation or treatment other than awaiting admission to adequate facility elsewhere\n --CHILD--> [QB12.0] Organ transplant candidate", "[QB12.Z] Waiting period for investigation or treatment other than awaiting admission to adequate facility elsewhere, unspecified\n --PARENT--> [QB12] Waiting period for investigation or treatment other than awaiting admission to adequate facility elsewhere\n --CHILD--> [QB12.0] Organ transplant candidate", "[QB12.Z] Waiting period for investigation or treatment other than awaiting admission to adequate facility elsewhere, unspecified\n --PARENT--> [QB12] Waiting period for investigation or treatment other than awaiting admission to adequate facility elsewhere\n --CHILD--> [QB12.0] Organ transplant candidate" ]
QB11
Person awaiting admission to adequate facility elsewhere
[ { "from_icd11": "QB11", "icd10_code": "Z751", "icd10_title": "Person awaiting admission to adequate facility elsewhere" }, { "from_icd11": "QB12.Z", "icd10_code": "Z752", "icd10_title": "Other waiting period for investigation and treatment" }, { "from_icd11": "4A01.03", "icd10_code": "D807", "icd10_title": "Transient hypogammaglobulinemia of infancy" }, { "from_icd11": "QB63.Z", "icd10_code": "Z9484", "icd10_title": "Stem cells transplant status" }, { "from_icd11": "QB63.Z", "icd10_code": "Z9481", "icd10_title": "Bone marrow transplant status" }, { "from_icd11": "QB63.Z", "icd10_code": "Z9489", "icd10_title": "Other transplanted organ and tissue status" }, { "from_icd11": "QB63.Z", "icd10_code": "Z9483", "icd10_title": "Pancreas transplant status" }, { "from_icd11": "QB63.Z", "icd10_code": "Z9482", "icd10_title": "Intestine transplant status" }, { "from_icd11": "QB63.Z", "icd10_code": "Z949", "icd10_title": "Transplanted organ and tissue status, unspecified" }, { "from_icd11": "QB63.Z", "icd10_code": "Z94", "icd10_title": "Transplanted organ and tissue status" }, { "from_icd11": "QB63.Z", "icd10_code": "Z943", "icd10_title": "Heart and lungs transplant status" }, { "from_icd11": "QB63.Z", "icd10_code": "Z948", "icd10_title": "Other transplanted organ and tissue status" }, { "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" } ]
Z751
Person awaiting admission to adequate facility elsewhere
Two months later, after six doses of adalimumab, she developed malaise with liver damage that continued after the discontinuation of adalimumab. A blood test three months after discontinuation showed the following: AST 240 U/L, ALT 224 U/L, alkaline phosphatase 723 U/L (normal 104–338) and GGT 228 U/L. Whilst serological tests for hepatitis A, B, and C viruses, Epstein-Barr virus, and cytomegalovirus were all negative, her serum immunoglobulin G levels were elevated and homogeneous and speckled-type ANAs were both present at titers of 1 : 160. Anti-smooth muscle antibody, anti-mitochondrial antibody, and anti-DNA antibody were negative. A percutaneous liver biopsy four months after discontinuation of adalimumab showed marked portal lymphoplasmacytic inflammation with periportal interface hepatitis and scattered lobular necroinflammatory changes . Accordingly, we diagnosed the patient as AIH and this was confirmed using simplified international diagnostic criteria (score 8 points; definite AIH ≥ 7) . The patient was treated with 30 mg of prednisolone per day (0.5 mg/kg/day: standard initial therapy regimen for AIH in Japan) for 2 weeks with the reduction of the dose by 5 mg every 2 weeks, and the maintenance dose was set at 5 mg per day. Two months later, her hepatobiliary enzymes returned to normal. While the patient is still under the maintenance therapy, the relapse of AIH has not been observed.
4.082031
0.968262
sec[1]/p[1]
en
0.999998
24082887
https://doi.org/10.1155/2013/561748
[ "adalimumab", "discontinuation", "anti", "antibody", "liver", "hepatitis", "maintenance", "doses", "malaise", "damage" ]
[ { "code": "BB02.3", "title": "Acquired pulmonary arterial tree abnormality" }, { "code": "AB18", "title": "Discontinuity or dislocation of ear ossicles" }, { "code": "LA85.40", "title": "Common arterial trunk with aortic dominance" }, { "code": "QA7A", "title": "Inappropriate stoppage or discontinuation of drug without injury or harm" }, { "code": "PL13.A", "title": "Inappropriate stoppage or discontinuation of drug, as mode of injury or harm" }, { "code": "JA86.Y", "title": "Maternal care for other specified fetal problems" }, { "code": "MB23.1", "title": "Antisocial behaviour" }, { "code": "3B4Z", "title": "Coagulation defects, unspecified" }, { "code": "4A45.Z", "title": "Antiphospholipid syndrome, unspecified" }, { "code": "4A43.Y", "title": "Other specified overlap non-organ specific systemic autoimmune disease" } ]
=== ICD-11 CODES FOUND === [BB02.3] Acquired pulmonary arterial tree abnormality Definition: A postnatal pathological change in form or function of the pulmonary arterial tree. Also known as: Acquired pulmonary arterial tree abnormality | Acquired discontinuity of pulmonary arteries | Acquired left pulmonary artery stenosis | Postprocedural left pulmonary artery stenosis | Acquired pulmonary arterial dissection [AB18] Discontinuity or dislocation of ear ossicles Also known as: Discontinuity or dislocation of ear ossicles | Discontinuity of ear ossicles | Dislocation of ear ossicles [LA85.40] Common arterial trunk with aortic dominance Definition: A congenital cardiovascular malformation in which a common arterial trunk is associated with an unobstructed aortic arch. Also known as: Common arterial trunk with aortic dominance | Truncus arteriosus with aortic dominance | truncus arteriosus with no aortic obstruction | Common arterial trunk with aortic dominance and both pulmonary arteries arising from trunk | Truncus arteriosus with aortic dominance and both pulmonary arteries arising from the trunk [QA7A] Inappropriate stoppage or discontinuation of drug without injury or harm Definition: Drug administration cancelled before prescribed or patient stopped taking drug without provider instructions. No injury or harm occurred as a result. Also known as: Inappropriate stoppage or discontinuation of drug without injury or harm Excludes: Inappropriate stoppage or discontinuation of drug, as mode of injury or harm [PL13.A] Inappropriate stoppage or discontinuation of drug, as mode of injury or harm Also known as: Inappropriate stoppage or discontinuation of drug, as mode of injury or harm | inappropriate interruption of drug | medication incorrectly stopped | medication error due to stopping administration of drug or substance incorrectly [JA86.Y] Maternal care for other specified fetal problems Also known as: Maternal care for other specified fetal problems | Maternal care for other isoimmunization | Isoimmunization NOS | maternal antibodies NOS | pregnancy management affected by incompatibility of blood groups NOS [MB23.1] Antisocial behaviour Definition: Behaviour in which the basic rights of others or major age-appropriate societal norms, rules, or laws, are violated. Also known as: Antisocial behaviour | Child or adolescent antisocial behaviour [3B4Z] Coagulation defects, unspecified Also known as: Coagulation defects, unspecified | blood clotting disturbance | blood clotting defect | blood clotting factor deficiency | clotting abnormality [4A45.Z] Antiphospholipid syndrome, unspecified Also known as: Antiphospholipid syndrome, unspecified | Antiphospholipid syndrome | Hughes syndrome | Anticardiolipin syndrome [4A43.Y] Other specified overlap non-organ specific systemic autoimmune disease Also known as: Other specified overlap non-organ specific systemic autoimmune disease | Antisynthetase syndrome | Reynolds syndrome | Syndromic multisystem autoimmune disease due to ITCH deficiency | Eosinophilia myalgia syndrome === GRAPH WALKS === --- Walk 1 --- [BB02.3] Acquired pulmonary arterial tree abnormality Def: A postnatal pathological change in form or function of the pulmonary arterial tree.... --RELATED_TO--> [?] Postprocedural pulmonary trunk stenosis Def: Discrete narrowing of the luminal diameter of the pulmonary trunk (main pulmonary artery) (below the lower limit of normal adjusted for body size) that occurs during or after an intervention.... --PARENT--> [?] Postprocedural pulmonary arterial tree disorder Def: An event or occurrence affecting the pulmonary arterial tree that is associated with a healthcare intervention, is a departure from the desired course of events, and may cause, or be associated with, ... --- Walk 2 --- [BB02.3] Acquired pulmonary arterial tree abnormality Def: A postnatal pathological change in form or function of the pulmonary arterial tree.... --RELATED_TO--> [?] Postprocedural pulmonary arterial tree disorder Def: An event or occurrence affecting the pulmonary arterial tree that is associated with a healthcare intervention, is a departure from the desired course of events, and may cause, or be associated with, ... --CHILD--> [?] Postprocedural pulmonary trunk stenosis Def: Discrete narrowing of the luminal diameter of the pulmonary trunk (main pulmonary artery) (below the lower limit of normal adjusted for body size) that occurs during or after an intervention.... --- Walk 3 --- [AB18] Discontinuity or dislocation of ear ossicles --PARENT--> [?] Diseases of middle ear or mastoid Def: Middle ear, derived from the first pharyngeal (branchial) pouch; has the malleus and incus and stapes and includes the spaces of the epitympanum and mesotympanum and hypotympanum. The mastoid; normall... --CHILD--> [?] Otitis media --- Walk 4 --- [AB18] Discontinuity or dislocation of ear ossicles --PARENT--> [?] Diseases of middle ear or mastoid Def: Middle ear, derived from the first pharyngeal (branchial) pouch; has the malleus and incus and stapes and includes the spaces of the epitympanum and mesotympanum and hypotympanum. The mastoid; normall... --RELATED_TO--> [?] Congenital conductive hearing loss --- Walk 5 --- [LA85.40] Common arterial trunk with aortic dominance Def: A congenital cardiovascular malformation in which a common arterial trunk is associated with an unobstructed aortic arch.... --PARENT--> [LA85.4] Common arterial trunk Def: A congenital cardiovascular malformation in which a single arterial trunk arises from the heart, giving origin sequentially to the coronary arteries, one or more pulmonary arteries, and the systemic a... --CHILD--> [LA85.40] Common arterial trunk with aortic dominance Def: A congenital cardiovascular malformation in which a common arterial trunk is associated with an unobstructed aortic arch.... --- Walk 6 --- [LA85.40] Common arterial trunk with aortic dominance Def: A congenital cardiovascular malformation in which a common arterial trunk is associated with an unobstructed aortic arch.... --PARENT--> [LA85.4] Common arterial trunk Def: A congenital cardiovascular malformation in which a single arterial trunk arises from the heart, giving origin sequentially to the coronary arteries, one or more pulmonary arteries, and the systemic a... --CHILD--> [LA85.40] Common arterial trunk with aortic dominance Def: A congenital cardiovascular malformation in which a common arterial trunk is associated with an unobstructed aortic arch....
[ "[BB02.3] Acquired pulmonary arterial tree abnormality\n Def: A postnatal pathological change in form or function of the pulmonary arterial tree....\n --RELATED_TO--> [?] Postprocedural pulmonary trunk stenosis\n Def: Discrete narrowing of the luminal diameter of the pulmonary trunk (main pulmonary artery) (below the lower limit of normal adjusted for body size) that occurs during or after an intervention....\n --PARENT--> [?] Postprocedural pulmonary arterial tree disorder\n Def: An event or occurrence affecting the pulmonary arterial tree that is associated with a healthcare intervention, is a departure from the desired course of events, and may cause, or be associated with, ...", "[BB02.3] Acquired pulmonary arterial tree abnormality\n Def: A postnatal pathological change in form or function of the pulmonary arterial tree....\n --RELATED_TO--> [?] Postprocedural pulmonary arterial tree disorder\n Def: An event or occurrence affecting the pulmonary arterial tree that is associated with a healthcare intervention, is a departure from the desired course of events, and may cause, or be associated with, ...\n --CHILD--> [?] Postprocedural pulmonary trunk stenosis\n Def: Discrete narrowing of the luminal diameter of the pulmonary trunk (main pulmonary artery) (below the lower limit of normal adjusted for body size) that occurs during or after an intervention....", "[AB18] Discontinuity or dislocation of ear ossicles\n --PARENT--> [?] Diseases of middle ear or mastoid\n Def: Middle ear, derived from the first pharyngeal (branchial) pouch; has the malleus and incus and stapes and includes the spaces of the epitympanum and mesotympanum and hypotympanum. The mastoid; normall...\n --CHILD--> [?] Otitis media", "[AB18] Discontinuity or dislocation of ear ossicles\n --PARENT--> [?] Diseases of middle ear or mastoid\n Def: Middle ear, derived from the first pharyngeal (branchial) pouch; has the malleus and incus and stapes and includes the spaces of the epitympanum and mesotympanum and hypotympanum. The mastoid; normall...\n --RELATED_TO--> [?] Congenital conductive hearing loss", "[LA85.40] Common arterial trunk with aortic dominance\n Def: A congenital cardiovascular malformation in which a common arterial trunk is associated with an unobstructed aortic arch....\n --PARENT--> [LA85.4] Common arterial trunk\n Def: A congenital cardiovascular malformation in which a single arterial trunk arises from the heart, giving origin sequentially to the coronary arteries, one or more pulmonary arteries, and the systemic a...\n --CHILD--> [LA85.40] Common arterial trunk with aortic dominance\n Def: A congenital cardiovascular malformation in which a common arterial trunk is associated with an unobstructed aortic arch....", "[LA85.40] Common arterial trunk with aortic dominance\n Def: A congenital cardiovascular malformation in which a common arterial trunk is associated with an unobstructed aortic arch....\n --PARENT--> [LA85.4] Common arterial trunk\n Def: A congenital cardiovascular malformation in which a single arterial trunk arises from the heart, giving origin sequentially to the coronary arteries, one or more pulmonary arteries, and the systemic a...\n --CHILD--> [LA85.40] Common arterial trunk with aortic dominance\n Def: A congenital cardiovascular malformation in which a common arterial trunk is associated with an unobstructed aortic arch...." ]
BB02.3
Acquired pulmonary arterial tree abnormality
[ { "from_icd11": "AB18", "icd10_code": "H7422", "icd10_title": "Discontinuity and dislocation of left ear ossicles" }, { "from_icd11": "AB18", "icd10_code": "H7421", "icd10_title": "Discontinuity and dislocation of right ear ossicles" }, { "from_icd11": "AB18", "icd10_code": "H742", "icd10_title": "Discontinuity and dislocation of ear ossicles" }, { "from_icd11": "QA7A", "icd10_code": "XXI", "icd10_title": "" }, { "from_icd11": "JA86.Y", "icd10_code": "O26841 ", "icd10_title": "" }, { "from_icd11": "JA86.Y", "icd10_code": "O26843 ", "icd10_title": "" }, { "from_icd11": "JA86.Y", "icd10_code": "O26849 ", "icd10_title": "" }, { "from_icd11": "JA86.Y", "icd10_code": "O3680X0 ", "icd10_title": "" }, { "from_icd11": "3B4Z", "icd10_code": "D688", "icd10_title": "Other specified coagulation defects" }, { "from_icd11": "3B4Z", "icd10_code": "D689", "icd10_title": "Coagulation defect, unspecified" }, { "from_icd11": "3B4Z", "icd10_code": "D699", "icd10_title": "Hemorrhagic condition, unspecified" }, { "from_icd11": "3B4Z", "icd10_code": "D698", "icd10_title": "Other specified hemorrhagic conditions" }, { "from_icd11": "3B4Z", "icd10_code": "D65-D69", "icd10_title": "" }, { "from_icd11": "3B4Z", "icd10_code": "D69", "icd10_title": "Purpura and other hemorrhagic conditions" }, { "from_icd11": "4A45.Z", "icd10_code": "D6861", "icd10_title": "Antiphospholipid syndrome" } ]
H7422
Discontinuity and dislocation of left ear ossicles
Plain x-ray films revealed a large, sclerotic lesion involving the right side of the frontal bone of the skull, extending to the unilateral frontal sinus . Further imaging with CT scan showed a diffuse sclerotic right-sided frontal lesion measuring approximately 9.5 × 12 × 1.5 cm involving the diploe with extensive mature periosteal new bone formation along the external table of the right frontal bone . The lesion extended across the midline and into the right frontal sinus. An MRI scan confirmed the osseous nature of the tumour and the absence of infiltration of the brain parenchyma . Fig. 1 Lateral X-ray of the skull shows an extensive osseous lesion of the diploe with periosteal new bone formation ( arrows ) along the external table of the anterior skull Fig. 2 a CT axial image shows a primarily sclerotic lesion involving the diploe ( white arrow ) extending across the midline ( black arrow ). b There is a polypoid mass in the right frontal sinus ( asterisk ). c Sagittal reconstruction shows the lesion ( white arrows ) and the polypoid mass ( asterisk ) Fig. 3 a Axial T1-weighted MR image shows thickening of the right frontal part of the diploe ( arrows ) with an underlying extensive low signal osseous lesion. b Axial T1-weighted MR image post gadolinium shows minimal enhancement of the periosteal part of the lesion ( arrows ). There is no evidence of abnormality related to the brain parenchyma
4.070313
0.736816
sec[1]/p[1]
en
0.999997
27525058
https://doi.org/10.1186/s13569-016-0054-2
[ "lesion", "frontal", "bone", "diploe", "arrows", "sclerotic", "involving", "skull", "sinus", "periosteal" ]
[ { "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": "9C82.4", "title": "Oculomotor apraxia" }, { "code": "CA0A.Y&XA91G8", "title": "Frontal sinus fistula" }, { "code": "CA0J.Y&XA91G8", "title": "Polyp of frontal sinus" }, { "code": "NA02.14", "title": "Fracture of frontal sinus of skull" }, { "code": "CA0C&XA91G8", "title": "Cyst of frontal sinus" } ]
=== 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 [9C82.4] Oculomotor apraxia Also known as: Oculomotor apraxia | Congenital ocular motor apraxia | Cogan’s congenital ocular motor apraxia | Saccadic palsy | Head thrust movement [NA02.14] Fracture of frontal sinus of skull Also known as: Fracture of frontal sinus of skull | fracture of frontal sinus | frontal sinus bone fracture === GRAPH WALKS === --- Walk 1 --- [FA5Z] Arthropathies, unspecified --PARENT--> [?] Arthropathies --CHILD--> [?] Infection related arthropathies Def: A disease of the joints, caused by an infection with a bacterial, viral, fungal, or parasitic source. Distinction is made between the following types of etiological relationship. a) direct infection ... --- Walk 2 --- [FA5Z] Arthropathies, unspecified --PARENT--> [?] Arthropathies --CHILD--> [?] Inflammatory arthropathies --- Walk 3 --- [FC0Z] Diseases of the musculoskeletal system or connective tissue, unspecified --PARENT--> [15] Diseases of the musculoskeletal system or connective tissue Def: This chapter contains diseases of musculoskeletal system and diseases of connective tissue.... --EXCLUDES--> [?] 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 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--> [?] Monogenic autoinflammatory syndromes Def: Monogenic hereditary autoinflammatory diseases characterised by apparently unprovoked generalised inflammation in the absence of infection or high titre autoantibodies.... --- 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--> [ME60.0] 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....
[ "[FA5Z] Arthropathies, unspecified\n --PARENT--> [?] Arthropathies\n --CHILD--> [?] Infection related arthropathies\n Def: A disease of the joints, caused by an infection with a bacterial, viral, fungal, or parasitic source.\n\nDistinction is made between the following types of etiological relationship.\na) direct infection ...", "[FA5Z] Arthropathies, unspecified\n --PARENT--> [?] Arthropathies\n --CHILD--> [?] Inflammatory arthropathies", "[FC0Z] Diseases of the musculoskeletal system or connective tissue, unspecified\n --PARENT--> [15] Diseases of the musculoskeletal system or connective tissue\n Def: This chapter contains diseases of musculoskeletal system and diseases of connective tissue....\n --EXCLUDES--> [?] 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...", "[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--> [?] Monogenic autoinflammatory syndromes\n Def: Monogenic hereditary autoinflammatory diseases characterised by apparently unprovoked generalised inflammation in the absence of infection or high titre autoantibodies....", "[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--> [ME60.0] 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...." ]
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": "9C82.4", "icd10_code": "H518", "icd10_title": "Other specified disorders of binocular movement" } ]
M00-M25
On review of the English language literature, the safety of systemic or catheter-directed thrombolysis in the setting of active hemorrhage or other absolute procedure contraindications has not been extensively studied. While sporadic case reports describe the safe use of intravenous or catheter-based thrombolysis in postsurgical patients, for example, large sample size prospective or retrospective investigations assessing the safety thrombolysis in actively bleeding patients have not been performed, likely due to unethical and unnecessary risk to study subjects. While recent major hemorrhage from a bleeding mycotic pseudoaneurysm constituted an absolute contraindication to thrombolysis in our case, we felt that lytic therapy could be pursued safely given the secure treatment of the bleeding source with stent exclusion prior to administration of thrombolytic medications. Although catheter-directed thrombolysis was not the only treatment option, with mechanical thrombectomy, stent-in-stent placement, surgical embolectomy, arterial bypass, and limb amputation as alternatives, it was felt to represent the treatment option with highest likelihood for success and lowest morbidity and mortality rates in our complex and medically unstable patient. Should the patient have developed any signs or symptoms suggesting hemorrhage during the course of therapy, thrombolysis would have been immediately terminated.
4.089844
0.595215
sec[2]/p[3]
en
0.999997
21603134
https://doi.org/10.1155/2011/264053
[ "thrombolysis", "catheter", "hemorrhage", "bleeding", "stent", "safety", "directed", "absolute", "while", "patients" ]
[ { "code": "QB62.Z", "title": "Attention to artificial openings, unspecified" }, { "code": "QB30.5", "title": "Fitting or adjustment of urinary device" }, { "code": "PK93.10", "title": "Gastroenterology or urology devices associated with injury or harm, urinary catheter" }, { "code": "PK90.1", "title": "Anaesthesiology devices associated with injury or harm, therapeutic, nonsurgical or rehabilitative devices" }, { "code": "PK91.2Y", "title": "Other specified cardiovascular devices associated with injury or harm, prosthetic or other implants, materials or accessory devices" }, { "code": "MG27", "title": "Haemorrhage, not elsewhere classified" }, { "code": "3B6Z", "title": "Coagulation defects, purpura or other haemorrhagic or related conditions, unspecified" }, { "code": "FB32.Y", "title": "Other specified disorders of muscles" }, { "code": "FA36.0", "title": "Effusion of joint containing blood" }, { "code": "JA41.Z", "title": "Antepartum haemorrhage, unspecified" } ]
=== ICD-11 CODES FOUND === [QB62.Z] Attention to artificial openings, unspecified Also known as: Attention to artificial openings, unspecified | Attention to artificial openings | toilet or cleansing of artificial opening | removal of catheter | passage of sounds or bougies [QB30.5] Fitting or adjustment of urinary device Also known as: Fitting or adjustment of urinary device | change of indwelling catheter | Removal of indwelling urinary catheter | removal of urinary catheter | removal of indwelling catheter [PK93.10] Gastroenterology or urology devices associated with injury or harm, urinary catheter Also known as: Gastroenterology or urology devices associated with injury or harm, urinary catheter | Gastroenterology or urology devices associated with adverse incidents, Foley catheter | Gastroenterology or urology devices associated with adverse incidents, indwelling urinary catheter | Mechanical complication of urinary catheter | Mechanical complication of urinary indwelling catheter Excludes: Circumstances associated with a surgical or other medical device influencing the episode of care without injury or harm [PK90.1] Anaesthesiology devices associated with injury or harm, therapeutic, nonsurgical or rehabilitative devices Definition: An anaesthesiology device was involved in an adverse incident that occurred in a therapeutic (nonsurgical) and rehabilitative task Also known as: Anaesthesiology devices associated with injury or harm, therapeutic, nonsurgical or rehabilitative devices | Anaesthesiology devices associated with injury or harm, spinal catheter | Mechanical complication of spinal catheter | Anaesthesiology devices associated with injury or harm, epidural catheter | Anaesthesiology devices associated with injury or harm, endotracheal tube Excludes: Circumstances associated with a surgical or other medical device influencing the episode of care without injury or harm [PK91.2Y] Other specified cardiovascular devices associated with injury or harm, prosthetic or other implants, materials or accessory devices Also known as: Other specified cardiovascular devices associated with injury or harm, prosthetic or other implants, materials or accessory devices | Cardiovascular devices associated with injury or harm, conduits | Mechanical complication of other cardiac and vascular devices and implants | Mechanical complication of artificial heart | Mechanical complication of vascular balloon implant or device [MG27] Haemorrhage, not elsewhere classified Definition: Bleeding or escape of blood from a vessel. Also known as: Haemorrhage, not elsewhere classified | arterial haemorrhage | bleeding | extravasation of blood | Haemorrhage NOS Excludes: Obstetric haemorrhage | Haemorrhage or haematoma complicating a procedure, not elsewhere classified | Fetal blood loss [3B6Z] Coagulation defects, purpura or other haemorrhagic or related conditions, unspecified Also known as: Coagulation defects, purpura or other haemorrhagic or related conditions, unspecified | Haemorrhagic condition, unspecified | unspecified hemorrhagic conditions | haemorrhagic disease NOS | haemorrhage diathesis [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 [FA36.0] Effusion of joint containing blood Also known as: Effusion of joint containing blood | bleeding into joint | hemarthrosis, site unspecified | haemarthrosis | joint haemorrhage Includes: haemarthrosis Excludes: Dislocation or strain or sprain of unspecified body region [JA41.Z] Antepartum haemorrhage, unspecified Also known as: Antepartum haemorrhage, unspecified | Antepartum haemorrhage | accidental antepartum haemorrhage | antepartum haemorrhage NOS | APH - [antepartum haemorrhage] === GRAPH WALKS === --- Walk 1 --- [QB62.Z] Attention to artificial openings, unspecified --PARENT--> [QB62] Attention to artificial openings --EXCLUDES--> [?] Fitting, adjustment or management of devices --- Walk 2 --- [QB62.Z] Attention to artificial openings, unspecified --PARENT--> [QB62] Attention to artificial openings --EXCLUDES--> [?] Presence of artificial opening --- Walk 3 --- [QB30.5] Fitting or adjustment of urinary device --PARENT--> [QB30] Adjustment or management of implanted devices --CHILD--> [QB30.0] Adjustment or management of implanted hearing device --- Walk 4 --- [QB30.5] Fitting or adjustment of urinary device --PARENT--> [QB30] Adjustment or management of implanted devices --CHILD--> [QB30.1] Adjustment or management of infusion pump --- Walk 5 --- [PK93.10] Gastroenterology or urology devices associated with injury or harm, urinary catheter --EXCLUDES--> [?] Circumstances associated with a surgical or other medical device influencing the episode of care without injury or harm --EXCLUDES--> [?] Mode of injury or harm associated with a surgical or other medical device, implant or graft --- Walk 6 --- [PK93.10] Gastroenterology or urology devices associated with injury or harm, urinary catheter --EXCLUDES--> [?] Circumstances associated with a surgical or other medical device influencing the episode of care without injury or harm --CHILD--> [?] Structural device failure without injury or harm Def: Mechanical or material device failure not related to the installation of the device without any documented injury or harm....
[ "[QB62.Z] Attention to artificial openings, unspecified\n --PARENT--> [QB62] Attention to artificial openings\n --EXCLUDES--> [?] Fitting, adjustment or management of devices", "[QB62.Z] Attention to artificial openings, unspecified\n --PARENT--> [QB62] Attention to artificial openings\n --EXCLUDES--> [?] Presence of artificial opening", "[QB30.5] Fitting or adjustment of urinary device\n --PARENT--> [QB30] Adjustment or management of implanted devices\n --CHILD--> [QB30.0] Adjustment or management of implanted hearing device", "[QB30.5] Fitting or adjustment of urinary device\n --PARENT--> [QB30] Adjustment or management of implanted devices\n --CHILD--> [QB30.1] Adjustment or management of infusion pump", "[PK93.10] Gastroenterology or urology devices associated with injury or harm, urinary catheter\n --EXCLUDES--> [?] Circumstances associated with a surgical or other medical device influencing the episode of care without injury or harm\n --EXCLUDES--> [?] Mode of injury or harm associated with a surgical or other medical device, implant or graft", "[PK93.10] Gastroenterology or urology devices associated with injury or harm, urinary catheter\n --EXCLUDES--> [?] Circumstances associated with a surgical or other medical device influencing the episode of care without injury or harm\n --CHILD--> [?] Structural device failure without injury or harm\n Def: Mechanical or material device failure not related to the installation of the device without any documented injury or harm...." ]
QB62.Z
Attention to artificial openings, unspecified
[ { "from_icd11": "QB62.Z", "icd10_code": "Z436", "icd10_title": "Encounter for attention to other artificial openings of urinary tract" }, { "from_icd11": "QB62.Z", "icd10_code": "Z434", "icd10_title": "Encounter for attention to other artificial openings of digestive tract" }, { "from_icd11": "QB62.Z", "icd10_code": "Z438", "icd10_title": "Encounter for attention to other artificial openings" }, { "from_icd11": "QB62.Z", "icd10_code": "Z439", "icd10_title": "Encounter for attention to unspecified artificial opening" }, { "from_icd11": "QB62.Z", "icd10_code": "Z43", "icd10_title": "Encounter for attention to artificial openings" }, { "from_icd11": "QB30.5", "icd10_code": "Z466", "icd10_title": "Encounter for fitting and adjustment of urinary device" }, { "from_icd11": "PK93.10", "icd10_code": "T83022A", "icd10_title": "Displacement of nephrostomy catheter, initial encounter" }, { "from_icd11": "PK93.10", "icd10_code": "T83020A", "icd10_title": "Displacement of cystostomy catheter, initial encounter" }, { "from_icd11": "PK93.10", "icd10_code": "T83032A", "icd10_title": "Leakage of nephrostomy catheter, initial encounter" }, { "from_icd11": "PK93.10", "icd10_code": "T83092A", "icd10_title": "Other mechanical complication of nephrostomy catheter, initial encounter" }, { "from_icd11": "PK93.10", "icd10_code": "T83021A", "icd10_title": "Displacement of indwelling urethral catheter, initial encounter" }, { "from_icd11": "PK93.10", "icd10_code": "T83028A", "icd10_title": "Displacement of other urinary catheter, initial encounter" }, { "from_icd11": "PK93.10", "icd10_code": "T83090A", "icd10_title": "Other mechanical complication of cystostomy catheter, initial encounter" }, { "from_icd11": "PK93.10", "icd10_code": "T83012A", "icd10_title": "Breakdown (mechanical) of nephrostomy catheter, initial encounter" }, { "from_icd11": "PK93.10", "icd10_code": "T83030A", "icd10_title": "Leakage of cystostomy catheter, initial encounter" } ]
Z436
Encounter for attention to other artificial openings of urinary tract
The child was placed in a semisitting position, assisted in removing the upper garment. The upper limb was abducted. The elbow was flexed. The head was slightly turned to the opposite side. The operating area was routinely disinfected. A sterile towel was laid. A high-frequency line array probe (a color ultrasound diagnostic instrument) and a 5 cm, 22G short oblique block needle were selected. The probe frequency was set at 6–13 MHz, which was placed in the center of the neck at the same level as the cricoid cartilage, and then moved outward to observe the trachea, thyroid gland, common carotid artery internal jugular vein, anterior oblique muscle, brachial plexus, and middle oblique muscle in turn. The location of the brachial plexus under the ultrasound image was found. The skin was punctured at the lateral part of the ultrasound probe. The needle advanced through the middle oblique muscle to ensure that it was located deep in the brachial plexus. 10–15 ml of local anesthetic (0.75% ropivacaine + 2% lidocaine) was injected after retraction without blood and a large amount of gas. The diffusion of local anesthetic was observed. The puncture needle retreated slowly to the subcutis, and then the angle of the needle entry was adjusted. The needle tip advanced to the upper anterior aspect of the brachial plexus, and 5–10 ml of the local anesthetic drug was injected again after no blood was retracted.
3.910156
0.84082
sec[2]/sec[1]/sec[0]/p[0]
en
0.999999
PMC9246567
https://doi.org/10.1155/2022/3383898
[ "needle", "oblique", "brachial", "plexus", "probe", "ultrasound", "muscle", "local", "anesthetic", "frequency" ]
[ { "code": "MB40.3", "title": "Anaesthesia of skin" }, { "code": "PA83.2&XE8D1", "title": "Accidental contact with needle" }, { "code": "LD25.1", "title": "Fronto-otopalatodigital syndromes" }, { "code": "QA8F", "title": "Needle stick without injury or harm" }, { "code": "PK81.F", "title": "Needle stick associated with injury or harm in therapeutic use" }, { "code": "LA51", "title": "Facial clefts" }, { "code": "JA82.2", "title": "Maternal care for transverse or oblique lie" }, { "code": "ND56.2", "title": "Fracture of unspecified body region" }, { "code": "DD51", "title": "Inguinal hernia" }, { "code": "9C80.5", "title": "Mechanical strabismus" } ]
=== ICD-11 CODES FOUND === [MB40.3] Anaesthesia of skin Definition: Partial or complete loss of sensation affecting the skin, most commonly affecting a circumscribed area and resulting from sensory nerve damage as from injury or leprosy. Also known as: Anaesthesia of skin | Hypoaesthesia of skin | Loss of cutaneous sensation | Numbness of skin | Loss of sensation Includes: Numbness of skin [LD25.1] Fronto-otopalatodigital syndromes Also known as: Fronto-otopalatodigital syndromes | Frontometaphyseal dysplasia | Melnick-Needles osteodysplasty | Otopalatodigital syndrome | Otopalatodigital syndrome type 1 [QA8F] Needle stick without injury or harm Also known as: Needle stick without injury or harm Excludes: Needle stick associated with injury or harm in therapeutic use [PK81.F] Needle stick associated with injury or harm in therapeutic use Also known as: Needle stick associated with injury or harm in therapeutic use [LA51] Facial clefts Definition: Any condition caused by failure of the structures of the face to correctly develop during the antenatal period. These conditions are characterised by a partition in bone, soft tissue, or skin of the face. Also known as: Facial clefts | Craniofacial clefts | Median facial cleft | Tessier number 0-14 and 30 facial cleft | Midline facial cleft Excludes: Frontofacionasal dysostosis | Frontonasal dysplasia [JA82.2] Maternal care for transverse or oblique lie Also known as: Maternal care for transverse or oblique lie | Maternal care for oblique presentation | Maternal care for prolapse of arm or hand | Maternal care for transverse presentation of fetus | transverse presentation [ND56.2] Fracture of unspecified body region Also known as: Fracture of unspecified body region | avulsion fracture of unspecified body site | comminuted fracture of unspecified body site | compression fracture of unspecified body site | fracture dislocation of unspecified body site Excludes: multiple fractures NOS [DD51] Inguinal hernia Definition: A hernia occurs when part of an internal organ bulges through a weak area of muscle. Most hernias occur in the abdomen. Inguinal hernia is the most common type and is in the groin. Also known as: Inguinal hernia | bubonocele | indirect inguinal hernia | direct inguinal hernia | oblique inguinal hernia Includes: bubonocele | scrotal hernia [9C80.5] Mechanical strabismus Definition: An abnormal binocular alignment caused by abnormalities of ocular movement in one or both eyes caused by damage to the extraocular muscles and/or other orbital structures. Mechanical strabismus is characterised by limitation of movements in one or more directions and variable strabismus. Also known as: Mechanical strabismus | acquired deformity of ocular muscle | Brown's sheath syndrome | Brown syndrome | Brown tendon sheath syndrome Includes: Brown's sheath syndrome === GRAPH WALKS === --- Walk 1 --- [MB40.3] Anaesthesia of skin Def: Partial or complete loss of sensation affecting the skin, most commonly affecting a circumscribed area and resulting from sensory nerve damage as from injury or leprosy.... --PARENT--> [MB40] Sensation disturbance --PARENT--> [?] Symptoms or signs involving the nervous system --- Walk 2 --- [MB40.3] Anaesthesia of skin Def: Partial or complete loss of sensation affecting the skin, most commonly affecting a circumscribed area and resulting from sensory nerve damage as from injury or leprosy.... --PARENT--> [MB40] Sensation disturbance --CHILD--> [MB40.1] Allodynia Def: Pain due to a normally non-painful stimulus... --- Walk 3 --- [LD25.1] Fronto-otopalatodigital syndromes --PARENT--> [LD25] Syndromes with face or limb anomalies as a major feature --PARENT--> [?] Multiple developmental anomalies or syndromes Def: Complex developmental anomalies involving more than one body system... --- Walk 4 --- [LD25.1] Fronto-otopalatodigital syndromes --PARENT--> [LD25] Syndromes with face or limb anomalies as a major feature --EXCLUDES--> [?] Freeman-Sheldon syndrome Def: Freeman-Sheldon syndrome is a rare congenital myopathic craniofacial syndrome. Considerable variability in severity is observed in this condition, but diagnosis requires the following: microstomia, wh... --- Walk 5 --- [QA8F] Needle stick without injury or harm --PARENT--> [?] Circumstances associated with other aspects of care influencing the episode of care without injury or harm --CHILD--> [QA82] Problem associated with physical transfer of patient without injury or harm Def: Fall, bump, slip, entanglement, drop of patient during movement with healthcare personnel, without documented injury or harm... --- Walk 6 --- [QA8F] Needle stick without injury or harm --PARENT--> [?] Circumstances associated with other aspects of care influencing the episode of care without injury or harm --CHILD--> [QA82] Problem associated with physical transfer of patient without injury or harm Def: Fall, bump, slip, entanglement, drop of patient during movement with healthcare personnel, without documented injury or harm...
[ "[MB40.3] Anaesthesia of skin\n Def: Partial or complete loss of sensation affecting the skin, most commonly affecting a circumscribed area and resulting from sensory nerve damage as from injury or leprosy....\n --PARENT--> [MB40] Sensation disturbance\n --PARENT--> [?] Symptoms or signs involving the nervous system", "[MB40.3] Anaesthesia of skin\n Def: Partial or complete loss of sensation affecting the skin, most commonly affecting a circumscribed area and resulting from sensory nerve damage as from injury or leprosy....\n --PARENT--> [MB40] Sensation disturbance\n --CHILD--> [MB40.1] Allodynia\n Def: Pain due to a normally non-painful stimulus...", "[LD25.1] Fronto-otopalatodigital syndromes\n --PARENT--> [LD25] Syndromes with face or limb anomalies as a major feature\n --PARENT--> [?] Multiple developmental anomalies or syndromes\n Def: Complex developmental anomalies involving more than one body system...", "[LD25.1] Fronto-otopalatodigital syndromes\n --PARENT--> [LD25] Syndromes with face or limb anomalies as a major feature\n --EXCLUDES--> [?] Freeman-Sheldon syndrome\n Def: Freeman-Sheldon syndrome is a rare congenital myopathic craniofacial syndrome. Considerable variability in severity is observed in this condition, but diagnosis requires the following: microstomia, wh...", "[QA8F] Needle stick without injury or harm\n --PARENT--> [?] Circumstances associated with other aspects of care influencing the episode of care without injury or harm\n --CHILD--> [QA82] Problem associated with physical transfer of patient without injury or harm\n Def: Fall, bump, slip, entanglement, drop of patient during movement with healthcare personnel, without documented injury or harm...", "[QA8F] Needle stick without injury or harm\n --PARENT--> [?] Circumstances associated with other aspects of care influencing the episode of care without injury or harm\n --CHILD--> [QA82] Problem associated with physical transfer of patient without injury or harm\n Def: Fall, bump, slip, entanglement, drop of patient during movement with healthcare personnel, without documented injury or harm..." ]
MB40.3
Anaesthesia of skin
[ { "from_icd11": "MB40.3", "icd10_code": "R200", "icd10_title": "Anesthesia of skin" }, { "from_icd11": "MB40.3", "icd10_code": "R201", "icd10_title": "Hypoesthesia of skin" }, { "from_icd11": "PA83.2&XE8D1", "icd10_code": "W461XXA", "icd10_title": "Contact with contaminated hypodermic needle, initial encounter" }, { "from_icd11": "PA83.2&XE8D1", "icd10_code": "W460XXA", "icd10_title": "Contact with hypodermic needle, initial encounter" }, { "from_icd11": "PA83.2&XE8D1", "icd10_code": "W46", "icd10_title": "Contact with hypodermic needle" }, { "from_icd11": "LD25.1", "icd10_code": "Q8789", "icd10_title": "Other specified congenital malformation syndromes, not elsewhere classified" }, { "from_icd11": "LD25.1", "icd10_code": "Q8781", "icd10_title": "Alport syndrome" }, { "from_icd11": "LD25.1", "icd10_code": "Q878", "icd10_title": "Other specified congenital malformation syndromes, not elsewhere classified" }, { "from_icd11": "QA8F", "icd10_code": "XXI", "icd10_title": "" }, { "from_icd11": "LA51", "icd10_code": "Q361", "icd10_title": "Cleft lip, median" }, { "from_icd11": "JA82.2", "icd10_code": "O322XX2", "icd10_title": "Maternal care for transverse and oblique lie, fetus 2" }, { "from_icd11": "JA82.2", "icd10_code": "O322XX0", "icd10_title": "Maternal care for transverse and oblique lie, not applicable or unspecified" }, { "from_icd11": "JA82.2", "icd10_code": "O322XX1", "icd10_title": "Maternal care for transverse and oblique lie, fetus 1" }, { "from_icd11": "JA82.2", "icd10_code": "O322", "icd10_title": "Maternal care for transverse and oblique lie" }, { "from_icd11": "ND56.2", "icd10_code": "T142", "icd10_title": "" } ]
R200
Anesthesia of skin
In our case, the patient no longer needed to be hospitalized for medical treatment alone as tube feeds could be given at home. Convincing the family and involved parties, however, that hospitalization was required in order to provide regular psychiatric follow-up for the potentially fatal disease of anorexia, was difficult. Various options were discussed: (1) that she remain hospitalized on the pediatrics ward for tube feeds, with monitoring and encouragement of caloric intake and weight gain, and treatment by the psychiatry consult service; (2) that she be transferred to the in-patient eating disorders unit while continuing NJ-tube feeds; (3) that she be discharged home, but monitored closely by her pediatrician, and that she be admitted to a partial psychiatric program with therapy from approximately 8.00 a.m. to 2.00 p.m.; (4) that she have the NJ tube removed in an attempt to begin liquid feeding and that she be immediately transferred to the in-patient eating disorders program; (5) that she have surgical correction, after which she could immediately resume oral feeds, and in-patient psychiatric evaluation; and (6) that she be discharged home with close follow-up by her pediatrician and an out-patient therapist, and that she be subsequently admitted to either the full in-patient or the partial in-patient eating disorders program after her weight had stabilized and the NJ tube could be removed.
3.519531
0.952637
sec[2]/p[1]
en
0.999998
19946542
https://doi.org/10.1186/1752-1947-3-127
[ "that", "tube", "feeds", "home", "psychiatric", "eating", "disorders", "program", "hospitalized", "weight" ]
[ { "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": "GA07.Z&XA3EF0", "title": "Inflammatory disease of fallopian tube" }, { "code": "JA01.1", "title": "Tubal pregnancy" }, { "code": "GB90.Y", "title": "Other specified disorders of kidney or ureter" }, { "code": "GB54", "title": "Tubulo-interstitial nephritis, not specified as acute or chronic" }, { "code": "AB10.Z", "title": "Disorders of Eustachian tube, unspecified" } ]
=== 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 [JA01.1] Tubal pregnancy Definition: A condition characterised by implantation of the embryo within the fallopian tube (ampullary, isthmus, interstitium) during pregnancy. Also known as: Tubal pregnancy | Fallopian pregnancy | fallopian tube pregnancy | Tubal abortion | Rupture of fallopian tube due to pregnancy Includes: Fallopian pregnancy | Tubal abortion [GB90.Y] Other specified disorders of kidney or ureter Also known as: Other specified disorders of kidney or ureter | Other secondary disorders of kidney or ureter | Other disorders of kidney and ureter NEC | Inflammatory diseases of the renal pelvis or the ureter without tubulo-interstitial nephritis | Infectious diseases of the renal pelvis or the ureter without tubulo-interstitial nephritis [GB54] Tubulo-interstitial nephritis, not specified as acute or chronic Definition: A disease characterised by inflammation of and damage to tubules or the interstitium of the kidney while sparing the glomeruli secondary to immune reaction or toxic agent. Also known as: Tubulo-interstitial nephritis, not specified as acute or chronic | tubulo-interstitial nephritis | renal disease with interstitial nephritis | Congenital pyelitis | Cystopyelitis Excludes: calculous pyelonephritis [AB10.Z] Disorders of Eustachian tube, unspecified Also known as: Disorders of Eustachian tube, unspecified | Disorders of Eustachian tube | auditory tube disorder | disease of Eustachian tube | Eustachian tube dysfunction === 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... --EXCLUDES--> [?] Headache, not elsewhere classified Def: Headache with characteristic features suggesting that it is a unique diagnostic entity, a finding or complaint, but not fulfilling criteria for any of the headache disorders described above.... --- Walk 3 --- [QA76] Medication or substance that is known to be an allergen without injury or harm Def: Medication that has previously been identified as an allergen to the patient is administered, but does not result in injury or harm.... --EXCLUDES--> [?] Medication or substance that is known to be an allergen, as mode of injury or harm --PARENT--> [?] Mode of injury or harm associated with exposure to a drug, medicament or biological substance --- Walk 4 --- [QA76] Medication or substance that is known to be an allergen without injury or harm Def: Medication that has previously been identified as an allergen to the patient is administered, but does not result in injury or harm.... --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--> [PL13.0] Overdose of substance, as mode of injury or harm Def: Incorrect dose - too high... --- 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 --PARENT--> [?] Causes of healthcare related harm or injury
[ "[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 --EXCLUDES--> [?] Headache, not elsewhere classified\n Def: Headache with characteristic features suggesting that it is a unique diagnostic entity, a finding or complaint, but not fulfilling criteria for any of the headache disorders described above....", "[QA76] Medication or substance that is known to be an allergen without injury or harm\n Def: Medication that has previously been identified as an allergen to the patient is administered, but does not result in injury or harm....\n --EXCLUDES--> [?] Medication or substance that is known to be an allergen, as mode of injury or harm\n --PARENT--> [?] Mode of injury or harm associated with exposure to a drug, medicament or biological substance", "[QA76] Medication or substance that is known to be an allergen without injury or harm\n Def: Medication that has previously been identified as an allergen to the patient is administered, but does not result in injury or harm....\n --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--> [PL13.0] Overdose of substance, as mode of injury or harm\n Def: Incorrect dose - too high...", "[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 --PARENT--> [?] Causes of healthcare related harm or injury" ]
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
On gross examination, a polypoid tumor, measuring 3.4 cm × 2.2 cm, with invasion to the pancreas was detected in the AmV . Microscopically, the tumor comprised both malignant squamous and glandular components . The majority of the tumor was composed of a moderately differentiated squamous cell carcinoma . Several focal signet ring-like glandular adenocarcinoma components were confined in the AmV . The resection margins were uninvolved, and regional lymph node involvement was identified in 2/46 retrieved nodes. The final diagnosis was ASC of the AmV, T3, N1, M0, stage IIB. The patient’s postoperative recovery was uneventful, and he was discharged 2 weeks after surgery. He was followed up 1 week after discharge and then regularly every 2 weeks thereafter. Routine biochemical and tumor markers were examined monthly, but no obvious change was observed. Adjuvant chemotherapy as Gemcitabine 1000 mg/m 2 per month combined with local radiation was arranged for this patient 6 weeks after the operation. Follow-up CT was scheduled for 3 months after surgery, but the patient presented with progressive jaundice 2 months after surgery. Abdominal CT revealed multiple metastatic nodules in the liver. This patient received palliative chemotherapy as Gemcitabine and Cisplatin once after the tumor progression. Nevertheless, his condition deteriorated, and the tumor progressed rapidly. He died 6 months after surgery.
3.894531
0.97998
sec[1]/p[1]
en
0.999996
23721111
https://doi.org/10.1186/1477-7819-11-124
[ "tumor", "squamous", "glandular", "components", "chemotherapy", "gemcitabine", "this", "gross", "polypoid", "measuring" ]
[ { "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": "9A01.3", "title": "Infectious blepharitis" }, { "code": "2E83.1", "title": "Benign osteogenic tumours of bone or articular cartilage of lower jaw" }, { "code": "CA0H.Y", "title": "Other specified diseases of vocal cords or larynx, not elsewhere classified" }, { "code": "2C31.Z", "title": "Cutaneous squamous cell carcinoma" }, { "code": "2C94.1", "title": "Squamous cell carcinoma of urinary bladder" } ]
=== 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 [9A01.3] Infectious blepharitis Definition: A condition of the eyelid, commonly caused by an infection with a bacterial source. This condition is characterised by pruritus, burning, scratchiness, excessive tearing, or crusty debris around the eyelashes. This condition may also present with lid erythema, collarettes, madarosis, trichiasis, or plugged meibomian glands. Transmission is by direct or indirect contact with an infected individual, endogenous spread, or through fomites. Also known as: Infectious blepharitis | blepharitis, nonulcerative | marginal blepharitis | ciliary blepharitis | anterior squamous lid disease Excludes: Blepharoconjunctivitis [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 [CA0H.Y] Other specified diseases of vocal cords or larynx, not elsewhere classified Also known as: Other specified diseases of vocal cords or larynx, not elsewhere classified | Other diseases of vocal cords | Vocal cord granuloma | Abscess of vocal cord | vocal cord abscess [2C31.Z] Cutaneous squamous cell carcinoma Also known as: Cutaneous squamous cell carcinoma | Squamous cell carcinoma of skin | Squamous cell epithelioma of skin | Cutaneous squamous cell carcinoma | SCC - [squamous cell carcinoma] of skin [2C94.1] Squamous cell carcinoma of urinary bladder Definition: A squamous cell carcinoma of the bladder arising from metaplastic epithelium. It represents less than 10% of bladder carcinomas. The exception is the Middle East along the Nile Valley, where it represents the most common form of carcinoma because of the endemic nature of schistosomiasis. Bladder squamous cell carcinoma is often associated with long-standing chronic inflammation of the bladder and usually has a poor prognosis. The diagnosis of squamous cell carcinoma of the bladder should be rese Also known as: Squamous cell carcinoma of urinary bladder | Squamous cell carcinoma of bladder === 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 --CHILD--> [2F90] Neoplasms of unknown behaviour of oral cavity or digestive organs --- Walk 3 --- [ME61] Subcutaneous swelling, mass or lump of uncertain or unspecified nature Def: One or more localised subcutaneous soft tissue masses of undetermined or unspecified nature... --EXCLUDES--> [?] Breast lump or mass female --PARENT--> [?] Symptoms, signs or clinical findings involving the female genital system --- Walk 4 --- [ME61] Subcutaneous swelling, mass or lump of uncertain or unspecified nature Def: One or more localised subcutaneous soft tissue masses of undetermined or unspecified nature... --EXCLUDES--> [?] Localised adiposity Def: A condition characterised by accumulation of adipose tissue in specific regions of the body.... --CHILD--> [?] Fatty apron --- Walk 5 --- [2E6Z] Carcinoma in situ of unspecified site --PARENT--> [?] In situ neoplasms, except of lymphoid, haematopoietic, central nervous system or related tissues --CHILD--> [2E61] Carcinoma in situ of other or unspecified digestive organs --- Walk 6 --- [2E6Z] Carcinoma in situ of unspecified site --PARENT--> [?] In situ neoplasms, except of lymphoid, haematopoietic, central nervous system or related tissues --CHILD--> [2E60] Carcinoma in situ of oral cavity, oesophagus or stomach
[ "[2F9Z] Neoplasms of unknown behaviour of unspecified site\n --PARENT--> [?] Neoplasms of unknown behaviour, except of lymphoid, haematopoietic, central nervous system or related tissues\n --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 --CHILD--> [2F90] Neoplasms of unknown behaviour of oral cavity or digestive organs", "[ME61] Subcutaneous swelling, mass or lump of uncertain or unspecified nature\n Def: One or more localised subcutaneous soft tissue masses of undetermined or unspecified nature...\n --EXCLUDES--> [?] Breast lump or mass female\n --PARENT--> [?] Symptoms, signs or clinical findings involving the female genital system", "[ME61] Subcutaneous swelling, mass or lump of uncertain or unspecified nature\n Def: One or more localised subcutaneous soft tissue masses of undetermined or unspecified nature...\n --EXCLUDES--> [?] Localised adiposity\n Def: A condition characterised by accumulation of adipose tissue in specific regions of the body....\n --CHILD--> [?] Fatty apron", "[2E6Z] Carcinoma in situ of unspecified site\n --PARENT--> [?] In situ neoplasms, except of lymphoid, haematopoietic, central nervous system or related tissues\n --CHILD--> [2E61] Carcinoma in situ of other or unspecified digestive organs", "[2E6Z] Carcinoma in situ of unspecified site\n --PARENT--> [?] In situ neoplasms, except of lymphoid, haematopoietic, central nervous system or related tissues\n --CHILD--> [2E60] Carcinoma in situ of oral cavity, oesophagus or stomach" ]
2F9Z
Neoplasms of unknown behaviour of unspecified site
[ { "from_icd11": "2F9Z", "icd10_code": "D487", "icd10_title": "Neoplasm of uncertain behavior of other specified sites" }, { "from_icd11": "2F9Z", "icd10_code": "D482", "icd10_title": "Neoplasm of uncertain behavior of peripheral nerves and autonomic nervous system" }, { "from_icd11": "2F9Z", "icd10_code": "D37-D48", "icd10_title": "" }, { "from_icd11": "2F9Z", "icd10_code": "D377", "icd10_title": "" }, { "from_icd11": "2F9Z", "icd10_code": "D48", "icd10_title": "Neoplasm of uncertain behavior of other and unspecified sites" }, { "from_icd11": "2F9Z", "icd10_code": "D489", "icd10_title": "Neoplasm of uncertain behavior, unspecified" }, { "from_icd11": "ME61", "icd10_code": "R2240", "icd10_title": "Localized swelling, mass and lump, unspecified lower limb" }, { "from_icd11": "ME61", "icd10_code": "R2232", "icd10_title": "Localized swelling, mass and lump, left upper limb" }, { "from_icd11": "ME61", "icd10_code": "R2242", "icd10_title": "Localized swelling, mass and lump, left lower limb" }, { "from_icd11": "ME61", "icd10_code": "R2231", "icd10_title": "Localized swelling, mass and lump, right upper limb" }, { "from_icd11": "ME61", "icd10_code": "R2241", "icd10_title": "Localized swelling, mass and lump, right lower limb" }, { "from_icd11": "ME61", "icd10_code": "R2233", "icd10_title": "Localized swelling, mass and lump, upper limb, bilateral" }, { "from_icd11": "ME61", "icd10_code": "R2243", "icd10_title": "Localized swelling, mass and lump, lower limb, bilateral" }, { "from_icd11": "ME61", "icd10_code": "R2230", "icd10_title": "Localized swelling, mass and lump, unspecified upper limb" }, { "from_icd11": "ME61", "icd10_code": "R220", "icd10_title": "Localized swelling, mass and lump, head" } ]
D487
Neoplasm of uncertain behavior of other specified sites
On the day of the surgery, the patient was premedicated with oral ranitidine 150 mg and diazepam 5 mg, two hours before surgery, with a sip of water, and injection glycopyrrolate 0.2 mg intramuscularly one hour before surgery. Preparation for fiberoptic intubation was done. Nasal patency was checked and the nasal cavity prepared with oxymetazoline nasal drops. In the operation room the patient was made to lie supine with the head adequately supported on three pillows and routine monitors, such as, the electrocardiogram, non-invasive blood pressure, and pulse oximeter and capnograph were placed. The IV line, with a 18 Gauge canula, was started. Anesthesia was induced with IV injection propofol 2 mg/kg, slowly, in titrated doses, with fentanyl 2 μg/kg. The anesthetist had to use a higher footstep than normal to get the desired level. We opted for fiberoptic bronchoscopy, but as the heart rate increased to 144/min and the blood pressure increased to 180/118 mmHg, we administered a further bolus dose of 50 mg of propofol to increase the depth of anesthesia. The patient's heart rate, and blood pressure stabilized, but the patient started desaturating with apneic spells, so we decided to abandon the procedure. The patient was allowed to wake up. Regional anesthesia was taken as the next option. Even after three attempts by expert hands no cerebrospinal fluid (CSF) was obtained through the spinal needle.
3.667969
0.958496
sec[1]/p[5]
en
0.999996
20532110
https://doi.org/10.4103/1658-354X.57879
[ "nasal", "blood", "pressure", "anesthesia", "injection", "fiberoptic", "three", "propofol", "heart", "premedicated" ]
[ { "code": "MA82.2", "title": "Nasality" }, { "code": "CA0Z", "title": "Upper respiratory tract disorders, unspecified" }, { "code": "CA0Y", "title": "Other specified upper respiratory tract disorders" }, { "code": "LA70.2", "title": "Choanal atresia" }, { "code": "NA00.3&XJ1C6", "title": "Haematoma of nose" }, { "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 === [MA82.2] Nasality Definition: Nasality (or resonance) refers to the quality of the voice that is determined by the balance of sound vibration in the oral, nasal, and pharyngeal cavities during speech. Abnormal resonance can occur when there is obstruction in one of the cavities, causing hyponasality, or when there is velopharyngeal dysfunction, causing hypernasality. This category should only be assigned when hyponasality or hypernasality is outside the limits of normal variation and results in reduced intelligibility and si Also known as: Nasality | Hypernasality | Hyponasality [CA0Z] Upper respiratory tract disorders, unspecified Also known as: Upper respiratory tract disorders, unspecified | Disorder of the nose, unspecified | Disease of nose, unspecified | nasal disease | Lesion of nose, unspecified [CA0Y] Other specified upper respiratory tract disorders Also known as: Other specified upper respiratory tract disorders | Acute adenoiditis | adenoid infection | Pharyngotonsillitis | tonsillopharyngitis [LA70.2] Choanal atresia Definition: Any condition in neonates, caused by failure of the nose to correctly develop during the antenatal period. This condition is characterised by narrowing or blockage of the nasal airway by tissue. This condition may also present with chest retraction unless child is breathing through mouth or crying, difficulty breathing, cyanosis, and inability to nurse and breathe at same time. Also known as: Choanal atresia | choanal fusion | atresia of nares | congenital stenosis of nares | congenital stenosis of choanae [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 --- [MA82.2] Nasality Def: Nasality (or resonance) refers to the quality of the voice that is determined by the balance of sound vibration in the oral, nasal, and pharyngeal cavities during speech. Abnormal resonance can occur ... --PARENT--> [MA82] Voice disturbances Def: Voice disturbances include dysphonia, aphonia, hypernasality and hyponasality, and other voice disturbances.... --CHILD--> [MA82.2] Nasality Def: Nasality (or resonance) refers to the quality of the voice that is determined by the balance of sound vibration in the oral, nasal, and pharyngeal cavities during speech. Abnormal resonance can occur ... --- Walk 2 --- [MA82.2] Nasality Def: Nasality (or resonance) refers to the quality of the voice that is determined by the balance of sound vibration in the oral, nasal, and pharyngeal cavities during speech. Abnormal resonance can occur ... --PARENT--> [MA82] Voice disturbances Def: Voice disturbances include dysphonia, aphonia, hypernasality and hyponasality, and other voice disturbances.... --CHILD--> [MA82.2] Nasality Def: Nasality (or resonance) refers to the quality of the voice that is determined by the balance of sound vibration in the oral, nasal, and pharyngeal cavities during speech. Abnormal resonance can occur ... --- Walk 3 --- [CA0Z] Upper respiratory tract disorders, unspecified --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 --- [CA0Z] Upper respiratory tract disorders, unspecified --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 5 --- [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 ... --CHILD--> [CA02] Acute pharyngitis Def: Acute pharyngitis is defined as an infection or irritation of the pharynx and/or tonsils and is a part of the common cold symptoms. The etiology is usually infectious, with most cases being of viral o... --- Walk 6 --- [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
[ "[MA82.2] Nasality\n Def: Nasality (or resonance) refers to the quality of the voice that is determined by the balance of sound vibration in the oral, nasal, and pharyngeal cavities during speech. Abnormal resonance can occur ...\n --PARENT--> [MA82] Voice disturbances\n Def: Voice disturbances include dysphonia, aphonia, hypernasality and hyponasality, and other voice disturbances....\n --CHILD--> [MA82.2] Nasality\n Def: Nasality (or resonance) refers to the quality of the voice that is determined by the balance of sound vibration in the oral, nasal, and pharyngeal cavities during speech. Abnormal resonance can occur ...", "[MA82.2] Nasality\n Def: Nasality (or resonance) refers to the quality of the voice that is determined by the balance of sound vibration in the oral, nasal, and pharyngeal cavities during speech. Abnormal resonance can occur ...\n --PARENT--> [MA82] Voice disturbances\n Def: Voice disturbances include dysphonia, aphonia, hypernasality and hyponasality, and other voice disturbances....\n --CHILD--> [MA82.2] Nasality\n Def: Nasality (or resonance) refers to the quality of the voice that is determined by the balance of sound vibration in the oral, nasal, and pharyngeal cavities during speech. Abnormal resonance can occur ...", "[CA0Z] Upper respiratory tract disorders, unspecified\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...", "[CA0Z] Upper respiratory tract disorders, unspecified\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 --CHILD--> [CA02] Acute pharyngitis\n Def: Acute pharyngitis is defined as an infection or irritation of the pharynx and/or tonsils and is a part of the common cold symptoms. The etiology is usually infectious, with most cases being of viral o...", "[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" ]
MA82.2
Nasality
[ { "from_icd11": "MA82.2", "icd10_code": "R4921", "icd10_title": "Hypernasality" }, { "from_icd11": "MA82.2", "icd10_code": "R4922", "icd10_title": "Hyponasality" }, { "from_icd11": "MA82.2", "icd10_code": "R492", "icd10_title": "Hypernasality and hyponasality" }, { "from_icd11": "CA0Z", "icd10_code": "J349", "icd10_title": "Unspecified disorder of nose and nasal sinuses" }, { "from_icd11": "CA0Z", "icd10_code": "J3489", "icd10_title": "Other specified disorders of nose and nasal sinuses" }, { "from_icd11": "CA0Z", "icd10_code": "J3481", "icd10_title": "Nasal mucositis (ulcerative)" }, { "from_icd11": "CA0Z", "icd10_code": "J398", "icd10_title": "Other specified diseases of upper respiratory tract" }, { "from_icd11": "CA0Z", "icd10_code": "J392", "icd10_title": "Other diseases of pharynx" }, { "from_icd11": "CA0Z", "icd10_code": "J399", "icd10_title": "Disease of upper respiratory tract, unspecified" }, { "from_icd11": "CA0Z", "icd10_code": "J00-J06", "icd10_title": "" }, { "from_icd11": "CA0Z", "icd10_code": "J30-J39", "icd10_title": "" }, { "from_icd11": "CA0Z", "icd10_code": "J34", "icd10_title": "Other and unspecified disorders of nose and nasal sinuses" }, { "from_icd11": "CA0Z", "icd10_code": "J348", "icd10_title": "Other specified disorders of nose and nasal sinuses" }, { "from_icd11": "CA0Z", "icd10_code": "J39", "icd10_title": "Other diseases of upper respiratory tract" }, { "from_icd11": "LA70.2", "icd10_code": "Q300", "icd10_title": "Choanal atresia" } ]
R4921
Hypernasality