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vignette-icd-enriched

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ECG showed anterior wall myocardial infarction ( Figure 1(a) ). The patient was immediately transferred to the cardiac catheterization laboratory and received successful emergency angioplasty/drug-eluting- (DE) stenting of the subtotally occluded left anterior descending artery ( Figure 1(b) ). Transthoracic echocardiography showed left ventricular hypertrophy, moderately reduced systolic left ventricular function (LVEF 40%) with anterior, septal, anteroseptal, inferior-apical, and apical hypo- and akinesia. The hemodynamically stable patient was monitored at the chest pain unit. CRP apheresis using the CRP adsorber (PentraSorb® CRP) within C-reactive Protein Apheresis in Acute Myocardial Infarction (CAMI-1) trial was performed 34 h and 58 h after the onset of symptoms. In each apheresis session, 6000 ml plasma was treated via peripheral venous access. Plasma CRP levels declined from 28.77 mg/l to 12.58 mg/l during the first apheresis session and from 24.17 mg/l to 11.55 mg/l during the second session, respectively (Figures 2(a) and 2(b) ). Figure 2 also shows cardiac enzyme progress over 72 h. Elevated creatinine kinase (CK), CK-MB, and troponin levels at admission documented acute STEMI. CRP levels, however, were normal at admission and, as a result of myocardial necrosis, increased with time . CRP apheresis efficiently counteracted acute phase CRP elevation and reduced peak CRP plasma levels.
4.082031
0.782227
sec[1]/p[1]
en
0.999996
30533227
https://doi.org/10.1155/2018/4767105
[ "apheresis", "myocardial", "session", "plasma", "infarction", "cardiac", "ventricular", "apical", "wall", "immediately" ]
[ { "code": "QB99", "title": "Apheresis" }, { "code": "BD1Z", "title": "Heart failure, unspecified" }, { "code": "BA41.Z", "title": "Acute myocardial infarction, unspecified" }, { "code": "BA52.Z", "title": "Coronary atherosclerosis, unspecified site" }, { "code": "LA8Z", "title": "Structural developmental anomaly of heart or great vessels, unspecified" }, { "code": "BA6Z", "title": "Ischaemic heart diseases, 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": "2A83.2", "title": "Solitary plasmacytoma" } ]
=== ICD-11 CODES FOUND === [QB99] Apheresis Also known as: Apheresis [BD1Z] Heart failure, unspecified Also known as: Heart failure, unspecified | myocardial failure | cardiac decompensation | cardiac failure | cardiac failure NOS [BA41.Z] Acute myocardial infarction, unspecified Also known as: Acute myocardial infarction, unspecified | Acute myocardial infarction | cardiac attack | heart attack | acute cardiac infarction [BA52.Z] Coronary atherosclerosis, unspecified site Also known as: Coronary atherosclerosis, unspecified site | Coronary atherosclerosis | cardiac sclerosis | coronary artery atherosclerosis | coronary artery sclerosis [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 [BA6Z] Ischaemic heart diseases, unspecified Also known as: Ischaemic heart diseases, unspecified | Ischaemic heart disease NOS | cardiac ischaemia, NOS | IHD - [ischaemic heart disease], NOS | cardiac ischemia [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 [2A83.2] Solitary plasmacytoma Definition: A single focus of clonal (malignant) plasma cells either in the bone or in another anatomic site without peripheral blood involvement. Also known as: Solitary plasmacytoma | solitary plasmacytoma without mention of remission | solitary myeloma | localised malignant plasma cell tumour NOS | plasmacytoma NOS Includes: solitary myeloma === GRAPH WALKS === --- Walk 1 --- [QB99] Apheresis --PARENT--> [?] Contact with health services for nonsurgical interventions not involving devices --CHILD--> [QB90] Contact with health services for ear piercing --- Walk 2 --- [QB99] Apheresis --PARENT--> [?] Contact with health services for nonsurgical interventions not involving devices --PARENT--> [?] Reasons for contact with the health services --- Walk 3 --- [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 4 --- [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 5 --- [BA41.Z] Acute myocardial infarction, unspecified --PARENT--> [BA41] Acute myocardial infarction Def: The term acute myocardial infarction (MI) should be used when there is evidence of myocardial necrosis in a clinical setting consistent with acute myocardial ischemia. Under these conditions any one o... --PARENT--> [?] Acute ischaemic heart disease --- Walk 6 --- [BA41.Z] Acute myocardial infarction, unspecified --PARENT--> [BA41] Acute myocardial infarction Def: The term acute myocardial infarction (MI) should be used when there is evidence of myocardial necrosis in a clinical setting consistent with acute myocardial ischemia. Under these conditions any one o... --EXCLUDES--> [?] Subsequent myocardial infarction Def: Infarction of any myocardial site, occurring within 4 weeks (28 days) from onset of a previous infarction...
[ "[QB99] Apheresis\n --PARENT--> [?] Contact with health services for nonsurgical interventions not involving devices\n --CHILD--> [QB90] Contact with health services for ear piercing", "[QB99] Apheresis\n --PARENT--> [?] Contact with health services for nonsurgical interventions not involving devices\n --PARENT--> [?] Reasons for contact with the health services", "[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 --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....", "[BA41.Z] Acute myocardial infarction, unspecified\n --PARENT--> [BA41] Acute myocardial infarction\n Def: The term acute myocardial infarction (MI) should be used when there is evidence of myocardial necrosis in a clinical setting consistent with acute myocardial ischemia. Under these conditions any one o...\n --PARENT--> [?] Acute ischaemic heart disease", "[BA41.Z] Acute myocardial infarction, unspecified\n --PARENT--> [BA41] Acute myocardial infarction\n Def: The term acute myocardial infarction (MI) should be used when there is evidence of myocardial necrosis in a clinical setting consistent with acute myocardial ischemia. Under these conditions any one o...\n --EXCLUDES--> [?] Subsequent myocardial infarction\n Def: Infarction of any myocardial site, occurring within 4 weeks (28 days) from onset of a previous infarction..." ]
QB99
Apheresis
[ { "from_icd11": "QB99", "icd10_code": "Z5189", "icd10_title": "Encounter for other specified aftercare" }, { "from_icd11": "QB99", "icd10_code": "Z51", "icd10_title": "Encounter for other aftercare and medical care" }, { "from_icd11": "QB99", "icd10_code": "Z518", "icd10_title": "Encounter for other specified aftercare" }, { "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" }, { "from_icd11": "BD1Z", "icd10_code": "I5042", "icd10_title": "Chronic combined systolic (congestive) and diastolic (congestive) heart failure" }, { "from_icd11": "BD1Z", "icd10_code": "I5043", "icd10_title": "Acute on chronic combined systolic (congestive) and diastolic (congestive) heart failure" }, { "from_icd11": "BD1Z", "icd10_code": "I5041", "icd10_title": "Acute combined systolic (congestive) and diastolic (congestive) heart failure" }, { "from_icd11": "BD1Z", "icd10_code": "I50812", "icd10_title": "Chronic right heart failure" }, { "from_icd11": "BD1Z", "icd10_code": "I50811", "icd10_title": "Acute right heart failure" } ]
Z5189
Encounter for other specified aftercare
Air leak syndrome is the overarching diagnosis for one or more pathologic air collections present outside of the respiratory tract. Seven classic presentations in neonates include pulmonary interstitial emphysema (PIE), pneumothorax, pneumomediastinum, pneumopericardium, pneumoperitoneum, subcutaneous emphysema, and systemic air embolism. Air leak occurs in approximately 10% of neonates with MAS for many presumed reasons including ball-valve effect of the meconium, ventilation-perfusion mismatch, surfactant inactivation, and parenchymal injury. While pneumoperitoneum is pathognomonic of perforation of an abdominal viscus , it rarely can result from air leak (incidence unknown) and, in such cases, is referred to as benign pneumoperitoneum (BPPT). Management of pneumoperitoneum resulting from a perforated viscus versus BPPT is quite different, the former representing a surgical emergency and the latter allowing the potential for conservative, nonoperative management. In a ventilated neonate with pneumoperitoneum, existing clinical evidence is ambiguous at delineating which cases may be amenable to initial observation alone. For clinicians caring for ill neonates, increased awareness of BPPT as a clinical entity might circumvent unnecessary surgeries and their inherent complications. We report a case of a term neonate with meconium aspiration syndrome (MAS) and air leak syndrome who developed BPPT.
4.265625
0.902832
sec[0]/p[0]
en
0.999995
31956461
https://doi.org/10.1155/2019/4238601
[ "pneumoperitoneum", "leak", "bppt", "neonates", "emphysema", "meconium", "viscus", "cases", "neonate", "overarching" ]
[ { "code": "DC51.Y", "title": "Other specified disorders of peritoneum or retroperitoneum" }, { "code": "KB27.4", "title": "Pneumoperitoneum, originating in the perinatal period, due to primary pulmonary air leak syndromes" }, { "code": "CB21.Z", "title": "Pneumothorax, unspecified" }, { "code": "MF50.5", "title": "Extravasation of urine" }, { "code": "NE81.3", "title": "Postsurgical leak" }, { "code": "GB0Y", "title": "Other specified diseases of the male genital system" }, { "code": "CB60", "title": "Tracheostomy malfunction" }, { "code": "5A00.00", "title": "Permanent congenital hypothyroidism with diffuse goitre" }, { "code": "KB45", "title": "Neonatal hypertension" }, { "code": "KB2D", "title": "Respiratory failure of newborn" } ]
=== ICD-11 CODES FOUND === [DC51.Y] Other specified disorders of peritoneum or retroperitoneum Also known as: Other specified disorders of peritoneum or retroperitoneum | Abdominal granuloma | Peritoneal granuloma | Epiploic appendagitis | Male frozen pelvis [KB27.4] Pneumoperitoneum, originating in the perinatal period, due to primary pulmonary air leak syndromes Also known as: Pneumoperitoneum, originating in the perinatal period, due to primary pulmonary air leak syndromes | Pneumoperitoneum originating in the perinatal period and secondary to primary pulmonary air leak syndromes [CB21.Z] Pneumothorax, unspecified Also known as: Pneumothorax, unspecified | Pneumothorax | pneumothorax NOS | air leak NOS | pleural air leak NOS [MF50.5] Extravasation of urine Also known as: Extravasation of urine | leakage of urine | Rupture of a renal calyx | Rupture of a renal fornix [NE81.3] Postsurgical leak Also known as: Postsurgical leak | postoperative leak | Postsurgical air leak | postoperative air leak | Postsurgical bile leak Excludes: Malfunction or complication of external stoma of digestive organs | Tracheostomy malfunction [GB0Y] Other specified diseases of the male genital system Also known as: Other specified diseases of the male genital system | Diseases of male genital organs | disease or disorder of male genitourinary system | Pain in scrotum | scrotal pain [CB60] Tracheostomy malfunction Also known as: Tracheostomy malfunction | tracheostomy dysfunction | status of malfunctioning tracheostomy | functional disturbance of tracheostomy | tracheostomy complications [5A00.00] Permanent congenital hypothyroidism with diffuse goitre Definition: A condition caused by a partial or complete loss of thyroid function due to failure of the thyroid to correctly develop during the antenatal period. This condition is characterised by a swollen, smooth thyroid gland, and in infants by a dull look, puffy face, and thick tongue that sticks out. This condition may also present with choking episodes, constipation, dry brittle hair, jaundice, lack of muscle tone, low hairline, poor feeding, short height, sleepiness, or sluggishness. Also known as: Permanent congenital hypothyroidism with diffuse goitre | congenital hypothyroidism with diffuse goitre | goitrous cretin | congenital diffuse goitre | congenital diffuse struma Excludes: transitory congenital goitre with normal function [KB45] Neonatal hypertension Definition: Hypertension is defined by a systolic blood pressure in a neonate which is >95th percentile for age and sex on 3 separate occasions Also known as: Neonatal hypertension | newborn hypertension | newborn essential hypertension | newborn benign essential hypertension | newborn benign hypertension [KB2D] Respiratory failure of newborn Definition: Acute or chronic respiratory failure in a newborn. Neonates in acute respiratory failure require respiratory support. Also known as: Respiratory failure of newborn | neonatal respiratory failure | inadequate pulmonary ventilation of newborn | newborn lung insufficiency | newborn pulmonary function inadequate === GRAPH WALKS === --- Walk 1 --- [DC51.Y] Other specified disorders of peritoneum or retroperitoneum --PARENT--> [DC51] Certain specified disorders of peritoneum or retroperitoneum --CHILD--> [DC51.0] Chylous ascites Def: Chylous ascites is a rare form of ascites caused by accumulation of lymph in the peritoneal cavity, usually due to intra-abdominal malignancy, liver cirrhosis or abdominal surgery complications, and p... --- Walk 2 --- [DC51.Y] Other specified disorders of peritoneum or retroperitoneum --PARENT--> [DC51] Certain specified disorders of peritoneum or retroperitoneum --PARENT--> [?] Diseases of peritoneum Def: This is the serous membrane that forms the lining of the abdominal cavity or the coelom—it covers most of the intra-abdominal (or coelomic) organs—in amniotes and some invertebrates.... --- Walk 3 --- [KB27.4] Pneumoperitoneum, originating in the perinatal period, due to primary pulmonary air leak syndromes --PARENT--> [KB27] Pulmonary air leak or related conditions originating in the perinatal period Def: Clinical syndrome due to free air from rupture of overdistended alveoli tracking into pulmonary interstitium, mediastinum, pleural cavity or subcutaneous tissues.... --CHILD--> [KB27.0] Interstitial emphysema originating in the perinatal period Def: Escape of air into the interstitium, lymphatics and venous circulation of the lungs resulting from rupture of small airways associated with a characteristic cystic appearance on chest X-ray, almost ex... --- Walk 4 --- [KB27.4] Pneumoperitoneum, originating in the perinatal period, due to primary pulmonary air leak syndromes --PARENT--> [KB27] Pulmonary air leak or related conditions originating in the perinatal period Def: Clinical syndrome due to free air from rupture of overdistended alveoli tracking into pulmonary interstitium, mediastinum, pleural cavity or subcutaneous tissues.... --CHILD--> [KB27.1] Pneumothorax originating in the perinatal period Def: Abnormal presence of air or other gas in the pleural cavity, usually secondary to tracking of free air from pulmonary interstitial emphysema, or rupture of subpleural blebs.... --- Walk 5 --- [CB21.Z] Pneumothorax, unspecified --PARENT--> [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.... --CHILD--> [CB21.Y] Other specified pneumothorax --- Walk 6 --- [CB21.Z] Pneumothorax, unspecified --PARENT--> [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.... --EXCLUDES--> [?] Traumatic pneumothorax
[ "[DC51.Y] Other specified disorders of peritoneum or retroperitoneum\n --PARENT--> [DC51] Certain specified disorders of peritoneum or retroperitoneum\n --CHILD--> [DC51.0] Chylous ascites\n Def: Chylous ascites is a rare form of ascites caused by accumulation of lymph in the peritoneal cavity, usually due to intra-abdominal malignancy, liver cirrhosis or abdominal surgery complications, and p...", "[DC51.Y] Other specified disorders of peritoneum or retroperitoneum\n --PARENT--> [DC51] Certain specified disorders of peritoneum or retroperitoneum\n --PARENT--> [?] Diseases of peritoneum\n Def: This is the serous membrane that forms the lining of the abdominal cavity or the coelom—it covers most of the intra-abdominal (or coelomic) organs—in amniotes and some invertebrates....", "[KB27.4] Pneumoperitoneum, originating in the perinatal period, due to primary pulmonary air leak syndromes\n --PARENT--> [KB27] Pulmonary air leak or related conditions originating in the perinatal period\n Def: Clinical syndrome due to free air from rupture of overdistended alveoli tracking into pulmonary interstitium, mediastinum, pleural cavity or subcutaneous tissues....\n --CHILD--> [KB27.0] Interstitial emphysema originating in the perinatal period\n Def: Escape of air into the interstitium, lymphatics and venous circulation of the lungs resulting from rupture of small airways associated with a characteristic cystic appearance on chest X-ray, almost ex...", "[KB27.4] Pneumoperitoneum, originating in the perinatal period, due to primary pulmonary air leak syndromes\n --PARENT--> [KB27] Pulmonary air leak or related conditions originating in the perinatal period\n Def: Clinical syndrome due to free air from rupture of overdistended alveoli tracking into pulmonary interstitium, mediastinum, pleural cavity or subcutaneous tissues....\n --CHILD--> [KB27.1] Pneumothorax originating in the perinatal period\n Def: Abnormal presence of air or other gas in the pleural cavity, usually secondary to tracking of free air from pulmonary interstitial emphysema, or rupture of subpleural blebs....", "[CB21.Z] Pneumothorax, unspecified\n --PARENT--> [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....\n --CHILD--> [CB21.Y] Other specified pneumothorax", "[CB21.Z] Pneumothorax, unspecified\n --PARENT--> [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....\n --EXCLUDES--> [?] Traumatic pneumothorax" ]
DC51.Y
Other specified disorders of peritoneum or retroperitoneum
[ { "from_icd11": "CB21.Z", "icd10_code": "J9383", "icd10_title": "Other pneumothorax" }, { "from_icd11": "CB21.Z", "icd10_code": "J9382", "icd10_title": "Other air leak" }, { "from_icd11": "CB21.Z", "icd10_code": "J9381", "icd10_title": "Chronic pneumothorax" }, { "from_icd11": "CB21.Z", "icd10_code": "J939", "icd10_title": "Pneumothorax, unspecified" }, { "from_icd11": "CB21.Z", "icd10_code": "J938", "icd10_title": "Other pneumothorax and air leak" }, { "from_icd11": "CB21.Z", "icd10_code": "J90-J94", "icd10_title": "" }, { "from_icd11": "CB21.Z", "icd10_code": "J93", "icd10_title": "Pneumothorax and air leak" }, { "from_icd11": "MF50.5", "icd10_code": "R390", "icd10_title": "Extravasation of urine" }, { "from_icd11": "CB60", "icd10_code": "J9503", "icd10_title": "Malfunction of tracheostomy stoma" }, { "from_icd11": "CB60", "icd10_code": "J9501", "icd10_title": "Hemorrhage from tracheostomy stoma" }, { "from_icd11": "CB60", "icd10_code": "J9502", "icd10_title": "Infection of tracheostomy stoma" }, { "from_icd11": "CB60", "icd10_code": "J9509", "icd10_title": "Other tracheostomy complication" }, { "from_icd11": "CB60", "icd10_code": "J9504", "icd10_title": "Tracheo-esophageal fistula following tracheostomy" }, { "from_icd11": "CB60", "icd10_code": "J950", "icd10_title": "Tracheostomy complications" }, { "from_icd11": "5A00.00", "icd10_code": "E071", "icd10_title": "Dyshormogenetic goiter" } ]
J9383
Other pneumothorax
Her mother contacted a pediatrician and scheduled an appointment for further evaluation the next day. Six hours prior to the office visit the following day, the patient mentioned feeling faint while walking down the stairs at home, with no loss of consciousness, which quickly resolved without any interventions. The patient’s mother also complained that the patient had a low-grade fever two days prior to the initial visit to the ED and denied having a history of asthma. On review of systems, she continued to endorse a persistent, non-productive cough, chest pressure, and shortness of breath, and had developed a sore throat. All other systems were non-contributory. Vital signs, in the supine position, were as follows: temperature of 98.0o F, pulse rate of 82 beats per minute, respiratory rate of 16 breaths per minute, and blood pressure of 116/72 mmHg. S1/S2 heart sounds were present but without murmurs. Pulmonary examination demonstrated clear breath sounds bilaterally. Five minutes later in the sitting position, pulse rate was 84 beats per minute and blood pressure was 112/70 mmHg. The patient was started on empiric antibiotic azithromycin for the treatment of suspected atypical community-acquired pneumonia (CAP) and was also prescribed an albuterol inhaler for suspected bronchospasm caused by cough syncope. At that time, she had blood taken to test for TSH, T4, and Mycoplasma pneumoniae IgM Ab.
3.626953
0.984375
sec[1]/p[14]
en
0.999995
32089974
https://doi.org/10.7759/cureus.6669
[ "pressure", "minute", "blood", "mother", "visit", "without", "that", "systems", "cough", "breath" ]
[ { "code": "EH90.Z", "title": "Pressure ulcer of unspecified grade" }, { "code": "MB23.L", "title": "Pressured speech" }, { "code": "MD30.Z", "title": "Chest pain, unspecified" }, { "code": "CB22.Y", "title": "Other specified diseases of mediastinum, not elsewhere classified" }, { "code": "BA2Z", "title": "Hypotension, unspecified" }, { "code": "ED5Y", "title": "Other specified disorders of epidermal keratinisation" }, { "code": "KD30.0", "title": "Birth depression with 5 minute Apgar score 0-3" }, { "code": "KD30.1", "title": "Birth depression with 5 minute Apgar score 4-6" }, { "code": "KB21.0", "title": "Severe birth asphyxia" }, { "code": "KB21.1", "title": "Mild and moderate birth asphyxia" } ]
=== ICD-11 CODES FOUND === [EH90.Z] Pressure ulcer of unspecified grade Also known as: Pressure ulcer of unspecified grade | Pressure ulceration | pressure injury | pressure ulcer | decubitus ulcer [MB23.L] Pressured speech Definition: Speech in which the person feels undue pressure to get the words out. The person’s speech is usually rapid, loud, and emphatic and may be difficult or impossible to interrupt. Frequently, the person talks without any social stimulation and may continue to talk even though no one is listening. Also known as: Pressured speech Excludes: Schizophrenia or other primary psychotic disorders | Bipolar or related disorders [MD30.Z] Chest pain, unspecified Also known as: Chest pain, unspecified | Pain in throat or chest | chest pain NOS | pain in chest | chest pressure [CB22.Y] Other specified diseases of mediastinum, not elsewhere classified Also known as: Other specified diseases of mediastinum, not elsewhere classified | Hernia of mediastinum | mediastinal hernia | mediastinal herniation | Infectious mediastinitis [BA2Z] Hypotension, unspecified Also known as: Hypotension, unspecified | hypopiesis | low blood pressure | arterial hypotension NOS | decreased blood pressure [ED5Y] Other specified disorders of epidermal keratinisation Also known as: Other specified disorders of epidermal keratinisation | Follicular digitate keratoses | Lichen spinulosus | Keratosis spinulosa | Keratosis circumscripta [KD30.0] Birth depression with 5 minute Apgar score 0-3 Definition: A condition characterised by cardiorespiratory and neurological depression, defined as an Apgar score between 0 to 3 at 5 minutes following birth. Also known as: Birth depression with 5 minute Apgar score 0-3 [KD30.1] Birth depression with 5 minute Apgar score 4-6 Definition: A condition characterised by cardiorespiratory and neurological depression, defined as an Apgar score between 4 and 6 at 5 minutes following birth. Also known as: Birth depression with 5 minute Apgar score 4-6 [KB21.0] Severe birth asphyxia Definition: Pulse less than 100 per minute at birth and falling or steady, respiration absent or gasping, colour poor, tone absent. Also known as: Severe birth asphyxia | severe perinatal hypoxia | asphyxia pallida of newborn | Asphyxia with 5-minute Apgar score 0-3 | newborn severe asphyxia [KB21.1] Mild and moderate birth asphyxia Definition: Normal respiration not established within one minute, but heart rate 100 or above, some muscle tone present, some response to stimulation. Also known as: Mild and moderate birth asphyxia | asphyxia livida of newborn | Asphyxia with 5-minute Apgar score 4-7 | Blue asphyxia === GRAPH WALKS === --- Walk 1 --- [EH90.Z] Pressure ulcer of unspecified grade --PARENT--> [EH90] Pressure ulceration Def: Pressure ulcers result from localised injury and ischaemic necrosis of skin and underlying tissues due to prolonged pressure, or pressure in combination with shear; bony prominences of the body are th... --CHILD--> [EH90.1] Pressure ulceration grade 2 Def: Pressure injury with partial thickness loss of dermis. It presents as a shallow open ulcer with a red or pink wound bed without slough or as a serum-filled or serosanguinous blister which may rupture.... --- Walk 2 --- [EH90.Z] Pressure ulcer of unspecified grade --PARENT--> [EH90] Pressure ulceration Def: Pressure ulcers result from localised injury and ischaemic necrosis of skin and underlying tissues due to prolonged pressure, or pressure in combination with shear; bony prominences of the body are th... --EXCLUDES--> [?] Erosion or ectropion of cervix uteri Def: 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... --- Walk 3 --- [MB23.L] Pressured speech Def: Speech in which the person feels undue pressure to get the words out. The person’s speech is usually rapid, loud, and emphatic and may be difficult or impossible to interrupt. Frequently, the person t... --EXCLUDES--> [?] Bipolar or related disorders Def: Bipolar and related disorders are episodic mood disorders defined by the occurrence of Manic, Mixed or Hypomanic episodes or symptoms. These episodes typically alternate over the course of these disor... --CHILD--> [?] Bipolar type II disorder Def: Bipolar type II disorder is an episodic mood disorder defined by the occurrence of one or more hypomanic episodes and at least one depressive episode. A hypomanic episode is a persistent mood state la... --- Walk 4 --- [MB23.L] Pressured speech Def: Speech in which the person feels undue pressure to get the words out. The person’s speech is usually rapid, loud, and emphatic and may be difficult or impossible to interrupt. Frequently, the person t... --EXCLUDES--> [?] Bipolar or related disorders Def: Bipolar and related disorders are episodic mood disorders defined by the occurrence of Manic, Mixed or Hypomanic episodes or symptoms. These episodes typically alternate over the course of these disor... --CHILD--> [?] Bipolar type II disorder Def: Bipolar type II disorder is an episodic mood disorder defined by the occurrence of one or more hypomanic episodes and at least one depressive episode. A hypomanic episode is a persistent mood state la... --- Walk 5 --- [MD30.Z] Chest pain, unspecified --PARENT--> [MD30] Pain in throat or chest Def: Pain in throat and chest means having pain sensation in throat or chest. Throat is a tube that carries food to oesophagus and air to windpipe and larynx. The technical name for throat is pharynx.... --EXCLUDES--> [?] Cervical spine pain Def: This is a condition which is usually characterised by pain or discomfort in the neck region and can be caused by numerous spinal problems. It may be a feature of virtually every disorder and disease t... --- Walk 6 --- [MD30.Z] Chest pain, unspecified --PARENT--> [MD30] Pain in throat or chest Def: Pain in throat and chest means having pain sensation in throat or chest. Throat is a tube that carries food to oesophagus and air to windpipe and larynx. The technical name for throat is pharynx.... --CHILD--> [MD30.Z] Chest pain, unspecified
[ "[EH90.Z] Pressure ulcer of unspecified grade\n --PARENT--> [EH90] Pressure ulceration\n Def: Pressure ulcers result from localised injury and ischaemic necrosis of skin and underlying tissues due to prolonged pressure, or pressure in combination with shear; bony prominences of the body are th...\n --CHILD--> [EH90.1] Pressure ulceration grade 2\n Def: Pressure injury with partial thickness loss of dermis. It presents as a shallow open ulcer with a red or pink wound bed without slough or as a serum-filled or serosanguinous blister which may rupture....", "[EH90.Z] Pressure ulcer of unspecified grade\n --PARENT--> [EH90] Pressure ulceration\n Def: Pressure ulcers result from localised injury and ischaemic necrosis of skin and underlying tissues due to prolonged pressure, or pressure in combination with shear; bony prominences of the body are th...\n --EXCLUDES--> [?] Erosion or ectropion of cervix uteri\n Def: 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...", "[MB23.L] Pressured speech\n Def: Speech in which the person feels undue pressure to get the words out. The person’s speech is usually rapid, loud, and emphatic and may be difficult or impossible to interrupt. Frequently, the person t...\n --EXCLUDES--> [?] Bipolar or related disorders\n Def: Bipolar and related disorders are episodic mood disorders defined by the occurrence of Manic, Mixed or Hypomanic episodes or symptoms. These episodes typically alternate over the course of these disor...\n --CHILD--> [?] Bipolar type II disorder\n Def: Bipolar type II disorder is an episodic mood disorder defined by the occurrence of one or more hypomanic episodes and at least one depressive episode. A hypomanic episode is a persistent mood state la...", "[MB23.L] Pressured speech\n Def: Speech in which the person feels undue pressure to get the words out. The person’s speech is usually rapid, loud, and emphatic and may be difficult or impossible to interrupt. Frequently, the person t...\n --EXCLUDES--> [?] Bipolar or related disorders\n Def: Bipolar and related disorders are episodic mood disorders defined by the occurrence of Manic, Mixed or Hypomanic episodes or symptoms. These episodes typically alternate over the course of these disor...\n --CHILD--> [?] Bipolar type II disorder\n Def: Bipolar type II disorder is an episodic mood disorder defined by the occurrence of one or more hypomanic episodes and at least one depressive episode. A hypomanic episode is a persistent mood state la...", "[MD30.Z] Chest pain, unspecified\n --PARENT--> [MD30] Pain in throat or chest\n Def: Pain in throat and chest means having pain sensation in throat or chest. Throat is a tube that carries food to oesophagus and air to windpipe and larynx. The technical name for throat is pharynx....\n --EXCLUDES--> [?] Cervical spine pain\n Def: This is a condition which is usually characterised by pain or discomfort in the neck region and can be caused by numerous spinal problems. It may be a feature of virtually every disorder and disease t...", "[MD30.Z] Chest pain, unspecified\n --PARENT--> [MD30] Pain in throat or chest\n Def: Pain in throat and chest means having pain sensation in throat or chest. Throat is a tube that carries food to oesophagus and air to windpipe and larynx. The technical name for throat is pharynx....\n --CHILD--> [MD30.Z] Chest pain, unspecified" ]
EH90.Z
Pressure ulcer of unspecified grade
[ { "from_icd11": "EH90.Z", "icd10_code": "L89623", "icd10_title": "Pressure ulcer of left heel, stage 3" }, { "from_icd11": "EH90.Z", "icd10_code": "L89621", "icd10_title": "Pressure ulcer of left heel, stage 1" }, { "from_icd11": "EH90.Z", "icd10_code": "L89899", "icd10_title": "Pressure ulcer of other site, unspecified stage" }, { "from_icd11": "EH90.Z", "icd10_code": "L89620", "icd10_title": "Pressure ulcer of left heel, unstageable" }, { "from_icd11": "EH90.Z", "icd10_code": "L89622", "icd10_title": "Pressure ulcer of left heel, stage 2" }, { "from_icd11": "EH90.Z", "icd10_code": "L89892", "icd10_title": "Pressure ulcer of other site, stage 2" }, { "from_icd11": "EH90.Z", "icd10_code": "L89519", "icd10_title": "Pressure ulcer of right ankle, unspecified stage" }, { "from_icd11": "EH90.Z", "icd10_code": "L89891", "icd10_title": "Pressure ulcer of other site, stage 1" }, { "from_icd11": "EH90.Z", "icd10_code": "L89610", "icd10_title": "Pressure ulcer of right heel, unstageable" }, { "from_icd11": "EH90.Z", "icd10_code": "L89893", "icd10_title": "Pressure ulcer of other site, stage 3" }, { "from_icd11": "EH90.Z", "icd10_code": "L89890", "icd10_title": "Pressure ulcer of other site, unstageable" }, { "from_icd11": "EH90.Z", "icd10_code": "L89629", "icd10_title": "Pressure ulcer of left heel, unspecified stage" }, { "from_icd11": "EH90.Z", "icd10_code": "L89619", "icd10_title": "Pressure ulcer of right heel, unspecified stage" }, { "from_icd11": "EH90.Z", "icd10_code": "L8945", "icd10_title": "Pressure ulcer of contiguous site of back, buttock and hip, unstageable" }, { "from_icd11": "EH90.Z", "icd10_code": "L89894", "icd10_title": "Pressure ulcer of other site, stage 4" } ]
L89623
Pressure ulcer of left heel, stage 3
Multiple laboratory and imaging studies were completed. Urine mucopolysaccharide screening negative. Normal CBC, LFTs, chemistry, creatinine kinase, TSH, lactate and ammonia levels. Normal pyruvate, carnitine, plasma and urine amino acids. Normal ceruloplasmin and copper levels. Initial very long‐chain fatty acid analysis showed moderate elevation of C26 and C26/C22 ratio with minimal elevation in C24 and C22; however, repeat analysis was normal. Normal CSF neopterin, tetrahydrobiopterin, homovanillic acid, 3‐O‐methyldopa, and 5‐hydroxyindoleacetic acid with otherwise normal CSF cell counts, protein, and glucose. Negative spinocerebellar ataxia type 2 and 3 genetic testing, as well as negative PARK2 testing (early‐onset Parkinsonism). Dopa‐responsive dystonia evaluation reported variant of unknown significance that was likely benign in the TH sequencing variant: IVS12 + 9 C>T. Normal glutaryl‐coA dehydrogenase enzyme activity in fibroblasts. Microarray completed at 6 years old was negative. MRI at 1 year reported nonspecific white matter changes, a small arachnoid cyst in the posterior fossa, J‐shaped sella, and mild tonsillar ectopy. Repeat MRI with MR spectroscopy completed at 2 years of age showed nonspecific white matter changes without spectroscopic abnormality. CXR and skeletal surveys were normal. Multiple EEGs were completed and were normal. Hearing and vision screening were also normal.
3.914063
0.93457
sec[1]/p[2]
en
0.999996
30455893
https://doi.org/10.1002/ccr3.1671
[ "acid", "multiple", "urine", "screening", "elevation", "repeat", "testing", "variant", "nonspecific", "white" ]
[ { "code": "5C73.Z", "title": "Acidosis, unspecified" }, { "code": "DA22.Z", "title": "Gastro-oesophageal reflux disease, unspecified" }, { "code": "DA41.2", "title": "Acid hypersecretion" }, { "code": "5B5C.Z", "title": "Vitamin B3 deficiency, unspecified" }, { "code": "5C64.3", "title": "Disorders of phosphorus metabolism or phosphatases" }, { "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 === [5C73.Z] Acidosis, unspecified Also known as: Acidosis, unspecified | Acidosis | acidosis NOS | metabolic acidaemia | lactic acidosis [DA22.Z] Gastro-oesophageal reflux disease, unspecified Also known as: Gastro-oesophageal reflux disease, unspecified | Gastro-oesophageal reflux disease | GORD - [gastro-oesophageal reflux disease] | gastroesophageal reflux disease | acid reflux disease [DA41.2] Acid hypersecretion Definition: Acid hypersecretion is a condition due to basal hypersecretion of gastric acid in the stomach, resulting in peptic ulcer and steatorrhoea. Also known as: Acid hypersecretion | acid peptic disease Excludes: Zollinger-Ellison syndrome [5B5C.Z] Vitamin B3 deficiency, unspecified Also known as: Vitamin B3 deficiency, unspecified | Vitamin B3 deficiency | nicotinic acid deficiency | vitamin B3 deficiency NOS | deficiency of niacin-tryptophan [5C64.3] Disorders of phosphorus metabolism or phosphatases Definition: Any condition caused by errors in phosphorus metabolism, or in phosphatase activity. Also known as: Disorders of phosphorus metabolism or phosphatases | disorders of phosphorus metabolism | Hypophosphatasia | Rathbun syndrome | Congenital hypophosphatasia Includes: Hypophosphatasia Excludes: Adult osteomalacia | Osteoporosis [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 --- [5C73.Z] Acidosis, unspecified --PARENT--> [5C73] Acidosis Def: Acidosis is an abnormally acidic state of the blood and tissues.... --RELATED_TO--> [?] Late metabolic acidosis of newborn Def: Mild to moderate metabolic acidosis occurring between 1 to 3 weeks of age in otherwise healthy premature infants fed cow's milk and accompanied by poor growth. This is thought to be due to excessive p... --- Walk 2 --- [5C73.Z] Acidosis, unspecified --PARENT--> [5C73] Acidosis Def: Acidosis is an abnormally acidic state of the blood and tissues.... --CHILD--> [5C73.0] Acute respiratory acidosis Def: This is an acute condition in which decreased ventilation (hypoventilation) causes increased blood carbon dioxide concentration and decreased pH (a condition generally called acidosis). Carbon dioxide... --- Walk 3 --- [DA22.Z] Gastro-oesophageal reflux disease, unspecified --PARENT--> [DA22] Gastro-oesophageal reflux disease Def: A condition which develops when the reflux of stomach contents causes troublesome symptoms and/or complications... --RELATED_TO--> [?] Gastro-oesophageal reflux disease in newborn Def: A condition which develops when the reflux of stomach contents causes the newborn to vomit with associated discomfort, difficulty feeding and/or weight loss.... --- Walk 4 --- [DA22.Z] Gastro-oesophageal reflux disease, unspecified --PARENT--> [DA22] Gastro-oesophageal reflux disease Def: A condition which develops when the reflux of stomach contents causes troublesome symptoms and/or complications... --PARENT--> [?] Diseases of oesophagus --- Walk 5 --- [DA41.2] Acid hypersecretion Def: Acid hypersecretion is a condition due to basal hypersecretion of gastric acid in the stomach, resulting in peptic ulcer and steatorrhoea.... --EXCLUDES--> [?] Zollinger-Ellison syndrome Def: A syndrome characterised by the presence of a gastrin-secreting tumour, usually in the pancreas or duodenum, resulting in increased gastric acidity and formation of gastric ulcers. Signs and symptoms ... --CHILD--> [?] Duodenal ulcer due to Zollinger-Ellison syndrome Def: Zollinger-Ellison syndrome is a rare cause of duodenal ulcer secondary to gastric acid hypersecretion due to unregulated gastrin release from a non-? cell endocrine tumour (gastrinoma) of pancreas or ... --- Walk 6 --- [DA41.2] Acid hypersecretion Def: Acid hypersecretion is a condition due to basal hypersecretion of gastric acid in the stomach, resulting in peptic ulcer and steatorrhoea.... --EXCLUDES--> [?] Zollinger-Ellison syndrome Def: A syndrome characterised by the presence of a gastrin-secreting tumour, usually in the pancreas or duodenum, resulting in increased gastric acidity and formation of gastric ulcers. Signs and symptoms ... --CHILD--> [?] Gastric ulcer due to Zollinger-Ellison syndrome Def: Zollinger-Ellison syndrome is a rare cause of gastric ulcer secondary to gastric acid hypersecretion due to unregulated gastrin release from a non-? cell endocrine tumour (gastrinoma) of pancreas or d...
[ "[5C73.Z] Acidosis, unspecified\n --PARENT--> [5C73] Acidosis\n Def: Acidosis is an abnormally acidic state of the blood and tissues....\n --RELATED_TO--> [?] Late metabolic acidosis of newborn\n Def: Mild to moderate metabolic acidosis occurring between 1 to 3 weeks of age in otherwise healthy premature infants fed cow's milk and accompanied by poor growth. This is thought to be due to excessive p...", "[5C73.Z] Acidosis, unspecified\n --PARENT--> [5C73] Acidosis\n Def: Acidosis is an abnormally acidic state of the blood and tissues....\n --CHILD--> [5C73.0] Acute respiratory acidosis\n Def: This is an acute condition in which decreased ventilation (hypoventilation) causes increased blood carbon dioxide concentration and decreased pH (a condition generally called acidosis). Carbon dioxide...", "[DA22.Z] Gastro-oesophageal reflux disease, unspecified\n --PARENT--> [DA22] Gastro-oesophageal reflux disease\n Def: A condition which develops when the reflux of stomach contents causes troublesome symptoms and/or complications...\n --RELATED_TO--> [?] Gastro-oesophageal reflux disease in newborn\n Def: A condition which develops when the reflux of stomach contents causes the newborn to vomit with associated discomfort, difficulty feeding and/or weight loss....", "[DA22.Z] Gastro-oesophageal reflux disease, unspecified\n --PARENT--> [DA22] Gastro-oesophageal reflux disease\n Def: A condition which develops when the reflux of stomach contents causes troublesome symptoms and/or complications...\n --PARENT--> [?] Diseases of oesophagus", "[DA41.2] Acid hypersecretion\n Def: Acid hypersecretion is a condition due to basal hypersecretion of gastric acid in the stomach, resulting in peptic ulcer and steatorrhoea....\n --EXCLUDES--> [?] Zollinger-Ellison syndrome\n Def: A syndrome characterised by the presence of a gastrin-secreting tumour, usually in the pancreas or duodenum, resulting in increased gastric acidity and formation of gastric ulcers. Signs and symptoms ...\n --CHILD--> [?] Duodenal ulcer due to Zollinger-Ellison syndrome\n Def: Zollinger-Ellison syndrome is a rare cause of duodenal ulcer secondary to gastric acid hypersecretion due to unregulated gastrin release from a non-? cell endocrine tumour (gastrinoma) of pancreas or ...", "[DA41.2] Acid hypersecretion\n Def: Acid hypersecretion is a condition due to basal hypersecretion of gastric acid in the stomach, resulting in peptic ulcer and steatorrhoea....\n --EXCLUDES--> [?] Zollinger-Ellison syndrome\n Def: A syndrome characterised by the presence of a gastrin-secreting tumour, usually in the pancreas or duodenum, resulting in increased gastric acidity and formation of gastric ulcers. Signs and symptoms ...\n --CHILD--> [?] Gastric ulcer due to Zollinger-Ellison syndrome\n Def: Zollinger-Ellison syndrome is a rare cause of gastric ulcer secondary to gastric acid hypersecretion due to unregulated gastrin release from a non-? cell endocrine tumour (gastrinoma) of pancreas or d..." ]
5C73.Z
Acidosis, unspecified
[ { "from_icd11": "5C73.Z", "icd10_code": "E872", "icd10_title": "Acidosis" }, { "from_icd11": "DA22.Z", "icd10_code": "K219", "icd10_title": "Gastro-esophageal reflux disease without esophagitis" }, { "from_icd11": "DA22.Z", "icd10_code": "K210", "icd10_title": "Gastro-esophageal reflux disease with esophagitis" }, { "from_icd11": "DA22.Z", "icd10_code": "K21", "icd10_title": "Gastro-esophageal reflux disease" }, { "from_icd11": "DA41.2", "icd10_code": "K31819", "icd10_title": "Angiodysplasia of stomach and duodenum without bleeding" }, { "from_icd11": "DA41.2", "icd10_code": "K31811", "icd10_title": "Angiodysplasia of stomach and duodenum with bleeding" }, { "from_icd11": "DA41.2", "icd10_code": "K3189", "icd10_title": "Other diseases of stomach and duodenum" }, { "from_icd11": "DA41.2", "icd10_code": "K3182", "icd10_title": "Dieulafoy lesion (hemorrhagic) of stomach and duodenum" }, { "from_icd11": "DA41.2", "icd10_code": "K3183", "icd10_title": "Achlorhydria" }, { "from_icd11": "DA41.2", "icd10_code": "K318", "icd10_title": "Other specified diseases of stomach and duodenum" }, { "from_icd11": "5C64.3", "icd10_code": "E8339", "icd10_title": "Other disorders of phosphorus metabolism" }, { "from_icd11": "5C64.3", "icd10_code": "E8332", "icd10_title": "Hereditary vitamin D-dependent rickets (type 1) (type 2)" }, { "from_icd11": "5C64.3", "icd10_code": "E8331", "icd10_title": "Familial hypophosphatemia" }, { "from_icd11": "5C64.3", "icd10_code": "E8330", "icd10_title": "Disorder of phosphorus metabolism, unspecified" }, { "from_icd11": "5C64.3", "icd10_code": "E833", "icd10_title": "Disorders of phosphorus metabolism and phosphatases" } ]
E872
Acidosis
A 53-year-old African-American woman with ESRD was transferred from dialysis clinic to the emergency room (ER) for evaluation of non-radiating and dull epigastric pain for two weeks associated with fever and chills during hemodialysis (HD). Three months ago, she was hospitalized and treated for Streptococcus pneumoniae and Enterobacter cloacae bacteremia. A year ago she was treated for S. maltophilia bacteremia secondary to an infected dialysis catheter. Past medical history was also significant for hypertension, atherosclerotic vascular disease pending elective coronary artery bypass graft (CABG) surgery, and sudden cardiac arrest followed by ICD placement. With the current presentation, both blood and catheter cultures obtained at the dialysis clinic were positive for S. maltophilia , prompting her subsequent arrival to the emergency room. She presented with a continuation of fever and chills, as well as tachycardia and episodic hypotension. She was noted to have mild epigastric tenderness. There was no surrounding erythema, discharge, or tenderness noted around the tunneled dialysis catheter on the right anterior chest. Initial workup showed elevated troponin and procalcitonin. Chest X-ray findings were suggestive for left lower lobe pneumonia. Within the ER, the patient's hypotension resolved with fluid resuscitation and intravenous levofloxacin therapy was started with blood cultures drawn.
3.783203
0.983887
sec[1]/p[0]
en
0.999998
31065471
https://doi.org/10.7759/cureus.4165
[ "dialysis", "catheter", "clinic", "emergency", "room", "epigastric", "fever", "chills", "treated", "bacteremia" ]
[ { "code": "QB94.Z", "title": "Care involving dialysis, unspecified" }, { "code": "QB94.1", "title": "Care involving extracorporeal dialysis" }, { "code": "9B73.0", "title": "Retinal detachment with retinal break" }, { "code": "QB94.2", "title": "Care involving peritoneal dialysis" }, { "code": "QB94.Y", "title": "Care involving other specified dialysis" }, { "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" } ]
=== ICD-11 CODES FOUND === [QB94.Z] Care involving dialysis, unspecified Also known as: Care involving dialysis, unspecified | Care involving dialysis | dialysis preparation and treatment | dialysis NOS [QB94.1] Care involving extracorporeal dialysis Also known as: Care involving extracorporeal dialysis | encounter for extracorporeal dialysis | encounter for dialysis NOS | encounter for renal dialysis NOS | aftercare involving extracorporeal dialysis [9B73.0] Retinal detachment with retinal break Also known as: Retinal detachment with retinal break | Rhegmatogenous retinal detachment | ruptured retina with detachment | retinal hole with detachment | Retinal detachment with giant retinal tear Includes: Rhegmatogenous retinal detachment [QB94.2] Care involving peritoneal dialysis Also known as: Care involving peritoneal dialysis | aftercare involving peritoneal dialysis | intermittent peritoneal dialysis | peritoneum dialysis [QB94.Y] Care involving other specified dialysis Also known as: Care involving other specified dialysis [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 === GRAPH WALKS === --- Walk 1 --- [QB94.Z] Care involving dialysis, unspecified --PARENT--> [QB94] Care involving dialysis Def: Care involving dialysis includes the preparation and maintenance of the patient and carer(s) on dialysis whether extracorporeal or peritoneal dialysis. This includes, but is not confined to: education... --CHILD--> [QB94.2] Care involving peritoneal dialysis --- Walk 2 --- [QB94.Z] Care involving dialysis, unspecified --PARENT--> [QB94] Care involving dialysis Def: Care involving dialysis includes the preparation and maintenance of the patient and carer(s) on dialysis whether extracorporeal or peritoneal dialysis. This includes, but is not confined to: education... --CHILD--> [QB94.0] Preparatory care for dialysis Def: Preparatory care for dialysis may include the assessment, education and counselling of the patient and carer(s) to facilitate psychosocial adjustment, choice of dialysis modality (including site – hom... --- Walk 3 --- [QB94.1] Care involving extracorporeal dialysis --PARENT--> [QB94] Care involving dialysis Def: Care involving dialysis includes the preparation and maintenance of the patient and carer(s) on dialysis whether extracorporeal or peritoneal dialysis. This includes, but is not confined to: education... --PARENT--> [?] Contact with health services for nonsurgical interventions not involving devices --- Walk 4 --- [QB94.1] Care involving extracorporeal dialysis --PARENT--> [QB94] Care involving dialysis Def: Care involving dialysis includes the preparation and maintenance of the patient and carer(s) on dialysis whether extracorporeal or peritoneal dialysis. This includes, but is not confined to: education... --EXCLUDES--> [?] Dependence on renal dialysis --- Walk 5 --- [9B73.0] Retinal detachment with retinal break --PARENT--> [9B73] Retinal detachments or breaks Def: Retinal breaks are full thickness openings in the neurosensory retina that can be in the form of a hole, a tear or a retinal dialysis. Retinal detachment is a condition in which the retina peels away ... --EXCLUDES--> [?] Separation of retinal layers --- Walk 6 --- [9B73.0] Retinal detachment with retinal break --PARENT--> [9B73] Retinal detachments or breaks Def: Retinal breaks are full thickness openings in the neurosensory retina that can be in the form of a hole, a tear or a retinal dialysis. Retinal detachment is a condition in which the retina peels away ... --CHILD--> [9B73.2] Retinal cysts Def: A retinal cyst is a closed sac, having a distinct membrane and division compared to the nearby tissue in retina that can either be congenital or acquired....
[ "[QB94.Z] Care involving dialysis, unspecified\n --PARENT--> [QB94] Care involving dialysis\n Def: Care involving dialysis includes the preparation and maintenance of the patient and carer(s) on dialysis whether extracorporeal or peritoneal dialysis. This includes, but is not confined to: education...\n --CHILD--> [QB94.2] Care involving peritoneal dialysis", "[QB94.Z] Care involving dialysis, unspecified\n --PARENT--> [QB94] Care involving dialysis\n Def: Care involving dialysis includes the preparation and maintenance of the patient and carer(s) on dialysis whether extracorporeal or peritoneal dialysis. This includes, but is not confined to: education...\n --CHILD--> [QB94.0] Preparatory care for dialysis\n Def: Preparatory care for dialysis may include the assessment, education and counselling of the patient and carer(s) to facilitate psychosocial adjustment, choice of dialysis modality (including site – hom...", "[QB94.1] Care involving extracorporeal dialysis\n --PARENT--> [QB94] Care involving dialysis\n Def: Care involving dialysis includes the preparation and maintenance of the patient and carer(s) on dialysis whether extracorporeal or peritoneal dialysis. This includes, but is not confined to: education...\n --PARENT--> [?] Contact with health services for nonsurgical interventions not involving devices", "[QB94.1] Care involving extracorporeal dialysis\n --PARENT--> [QB94] Care involving dialysis\n Def: Care involving dialysis includes the preparation and maintenance of the patient and carer(s) on dialysis whether extracorporeal or peritoneal dialysis. This includes, but is not confined to: education...\n --EXCLUDES--> [?] Dependence on renal dialysis", "[9B73.0] Retinal detachment with retinal break\n --PARENT--> [9B73] Retinal detachments or breaks\n Def: Retinal breaks are full thickness openings in the neurosensory retina that can be in the form of a hole, a tear or a retinal dialysis. Retinal detachment is a condition in which the retina peels away ...\n --EXCLUDES--> [?] Separation of retinal layers", "[9B73.0] Retinal detachment with retinal break\n --PARENT--> [9B73] Retinal detachments or breaks\n Def: Retinal breaks are full thickness openings in the neurosensory retina that can be in the form of a hole, a tear or a retinal dialysis. Retinal detachment is a condition in which the retina peels away ...\n --CHILD--> [9B73.2] Retinal cysts\n Def: A retinal cyst is a closed sac, having a distinct membrane and division compared to the nearby tissue in retina that can either be congenital or acquired...." ]
QB94.Z
Care involving dialysis, unspecified
[ { "from_icd11": "QB94.Z", "icd10_code": "Z4931", "icd10_title": "Encounter for adequacy testing for hemodialysis" }, { "from_icd11": "QB94.Z", "icd10_code": "Z4932", "icd10_title": "Encounter for adequacy testing for peritoneal dialysis" }, { "from_icd11": "QB94.Z", "icd10_code": "Z49", "icd10_title": "Encounter for care involving renal dialysis" }, { "from_icd11": "QB94.1", "icd10_code": "Z491", "icd10_title": "" }, { "from_icd11": "9B73.0", "icd10_code": "H33051", "icd10_title": "Total retinal detachment, right eye" }, { "from_icd11": "9B73.0", "icd10_code": "H33012", "icd10_title": "Retinal detachment with single break, left eye" }, { "from_icd11": "9B73.0", "icd10_code": "H33052", "icd10_title": "Total retinal detachment, left eye" }, { "from_icd11": "9B73.0", "icd10_code": "H33001", "icd10_title": "Unspecified retinal detachment with retinal break, right eye" }, { "from_icd11": "9B73.0", "icd10_code": "H33009", "icd10_title": "Unspecified retinal detachment with retinal break, unspecified eye" }, { "from_icd11": "9B73.0", "icd10_code": "H33059", "icd10_title": "Total retinal detachment, unspecified eye" }, { "from_icd11": "9B73.0", "icd10_code": "H33029", "icd10_title": "Retinal detachment with multiple breaks, unspecified eye" }, { "from_icd11": "9B73.0", "icd10_code": "H33039", "icd10_title": "Retinal detachment with giant retinal tear, unspecified eye" }, { "from_icd11": "9B73.0", "icd10_code": "H330", "icd10_title": "Retinal detachment with retinal break" }, { "from_icd11": "QB94.2", "icd10_code": "Z492", "icd10_title": "" }, { "from_icd11": "QB62.Z", "icd10_code": "Z436", "icd10_title": "Encounter for attention to other artificial openings of urinary tract" } ]
Z4931
Encounter for adequacy testing for hemodialysis
Regarding past medical history, radiologic, endoscopic, and pathologic data, the patient was initially diagnosed with a malignant nonepithelial lower rectal tumor of the unknown origin and staged as mrT3a mrN0 cM0. Being aware of primary colorectal sarcomas, their recurrence and progression patterns and a threatening rate of R1 and R2 resections, an institutional multidisciplinary board suggested curative surgery as a primary treatment option. Total mesorectal excision (TME) with complete mesocolic excision and central vascular ligation (CME/CVL) carried by an open approach was selected as proper extent of surgery. Standardized surgical technique in this case included complete left flexure mobilization, ligation of the inferior mesenteric artery at its origin near the aorta and inferior mesenteric vein just below the pancreatic tail with consecutive total mesorectal excision up to the level of the pelvic diaphragm . Accurate TME procedure had been exacerbated by severe fibrotic changes of surrounding pelvic tissues due to postoperative changes after iliac lymphadenectomy for cervical cancer and radiation-induced fibrosis as well. Regarding the significant fibrotic transformation of the anterior rectal wall with adjacent tissues, an intraoperative decision was made to avoid reconstruction aware of an estimated high risk of anastomotic leakage. Closure of the pelvic peritoneum was avoided as well.
4.039063
0.967285
sec[2]/p[0]
en
0.999998
31885968
https://doi.org/10.1155/2019/1610653
[ "excision", "pelvic", "regarding", "rectal", "origin", "aware", "total", "mesorectal", "complete", "ligation" ]
[ { "code": "FC00.3", "title": "Acquired deformity of pelvis" }, { "code": "GA34.Y", "title": "Other specified female pelvic pain associated with genital organs or menstrual cycle" }, { "code": "LB30.7", "title": "Ectopic or pelvic kidney" }, { "code": "MD82", "title": "Intra-abdominal or pelvic swelling, mass or lump" }, { "code": "GA05.Z", "title": "Female pelvic inflammatory diseases, unspecified" }, { "code": "QA15.1", "title": "Counselling related to sexual behaviour and orientation or sexual relationships of the person" }, { "code": "QA15.2", "title": "Counselling related to sexual behaviour and orientation or sexual relationships of third party" }, { "code": "QA15.0", "title": "Counselling related to sexual attitudes" }, { "code": "DB30.4", "title": "Stenosis of the rectum" }, { "code": "DB31.0&XA4KU2", "title": "Rectal fistula" } ]
=== ICD-11 CODES FOUND === [FC00.3] Acquired deformity of pelvis Also known as: Acquired deformity of pelvis | deformity of pelvis | pelvic deformity | ischium deformity | ilium deformity Excludes: Maternal care for disproportion | Obstructed labour due to maternal pelvic abnormality | Obstructed labour due to deformed pelvis [GA34.Y] Other specified female pelvic pain associated with genital organs or menstrual cycle Also known as: Other specified female pelvic pain associated with genital organs or menstrual cycle | Pelvic congestion syndrome | Pelvic varicosities | Female frozen pelvis | Female intrapelvic haemorrhage [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 [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 [GA05.Z] Female pelvic inflammatory diseases, unspecified Also known as: Female pelvic inflammatory diseases, unspecified | Female pelvic inflammatory diseases | PID - [pelvic inflammatory disease] | pelvic inflammatory disease NOS | Parametritis [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 [QA15.2] Counselling related to sexual behaviour and orientation or sexual relationships of third party Also known as: Counselling related to sexual behaviour and orientation or sexual relationships of third party | counselling for non-attending third party, related to sexual behaviour or orientation | Advice sought regarding sexual behaviour and orientation of child | Advice sought regarding sexual behaviour and orientation of partner | Advice sought regarding sexual behaviour and orientation of spouse [QA15.0] Counselling related to sexual attitudes Also known as: Counselling related to sexual attitudes | person concerned regarding embarrassment, timidity or other negative response to sexual matters [DB30.4] Stenosis of the rectum Definition: Rectal stenosis is defined as narrowing of the rectum. Also known as: Stenosis of the rectum | obstructed rectum | rectal stenosis | stricture of rectum | rectal obstruction === GRAPH WALKS === --- Walk 1 --- [FC00.3] Acquired deformity of pelvis --EXCLUDES--> [?] Obstructed labour due to deformed pelvis --CHILD--> [?] Flat pelvis with disproportion, causing obstructed labour --- Walk 2 --- [FC00.3] Acquired deformity of pelvis --EXCLUDES--> [?] Obstructed labour due to maternal pelvic abnormality Def: Obstructed labour means that, in spite of strong contractions of the uterus, the fetus cannot descend through the pelvis because there is an insurmountable barrier preventing its descent. Obstruction ... --CHILD--> [?] Obstructed labour due to pelvic inlet contraction --- Walk 3 --- [GA34.Y] Other specified female pelvic pain associated with genital organs or menstrual cycle --PARENT--> [GA34] Female pelvic pain associated with genital organs or menstrual cycle Def: A symptom affecting females, characterised by pain in the pelvic region associated with any of the genital organs or the menstrual cycle.... --PARENT--> [?] Diseases of the female genital system --- Walk 4 --- [GA34.Y] Other specified female pelvic pain associated with genital organs or menstrual cycle --PARENT--> [GA34] Female pelvic pain associated with genital organs or menstrual cycle Def: A symptom affecting females, characterised by pain in the pelvic region associated with any of the genital organs or the menstrual cycle.... --RELATED_TO--> [?] Interstitial cystitis Def: A condition characterised by inflammation of the urinary bladder and ureters. This condition may be associated with a malformation of, or injury to, the bladder epithelium, infection with toxins, an a... --- Walk 5 --- [LB30.7] Ectopic or pelvic kidney Def: A birth defect characterised by an abnormally positioned kidney; may be asymptomatic or result in urine blockage, infection or kidney stones... --PARENT--> [LB30] Structural developmental anomalies of kidneys Def: Any condition caused by failure of the kidneys to correctly develop during the antenatal period.... --PARENT--> [?] Structural developmental anomalies of the urinary system Def: Any condition caused by failure of the urinary system to correctly develop during the antenatal period.... --- Walk 6 --- [LB30.7] Ectopic or pelvic kidney Def: A birth defect characterised by an abnormally positioned kidney; may be asymptomatic or result in urine blockage, infection or kidney stones... --PARENT--> [LB30] Structural developmental anomalies of kidneys Def: Any condition caused by failure of the kidneys to correctly develop during the antenatal period.... --CHILD--> [LB30.1] Renal dysplasia Def: A condition characterised by abnormal development of one or both kidneys....
[ "[FC00.3] Acquired deformity of pelvis\n --EXCLUDES--> [?] Obstructed labour due to deformed pelvis\n --CHILD--> [?] Flat pelvis with disproportion, causing obstructed labour", "[FC00.3] Acquired deformity of pelvis\n --EXCLUDES--> [?] Obstructed labour due to maternal pelvic abnormality\n Def: Obstructed labour means that, in spite of strong contractions of the uterus, the fetus cannot descend through the pelvis because there is an insurmountable barrier preventing its descent. Obstruction ...\n --CHILD--> [?] Obstructed labour due to pelvic inlet contraction", "[GA34.Y] Other specified female pelvic pain associated with genital organs or menstrual cycle\n --PARENT--> [GA34] Female pelvic pain associated with genital organs or menstrual cycle\n Def: A symptom affecting females, characterised by pain in the pelvic region associated with any of the genital organs or the menstrual cycle....\n --PARENT--> [?] Diseases of the female genital system", "[GA34.Y] Other specified female pelvic pain associated with genital organs or menstrual cycle\n --PARENT--> [GA34] Female pelvic pain associated with genital organs or menstrual cycle\n Def: A symptom affecting females, characterised by pain in the pelvic region associated with any of the genital organs or the menstrual cycle....\n --RELATED_TO--> [?] Interstitial cystitis\n Def: A condition characterised by inflammation of the urinary bladder and ureters. This condition may be associated with a malformation of, or injury to, the bladder epithelium, infection with toxins, an a...", "[LB30.7] Ectopic or pelvic kidney\n Def: A birth defect characterised by an abnormally positioned kidney; may be asymptomatic or result in urine blockage, infection or kidney stones...\n --PARENT--> [LB30] Structural developmental anomalies of kidneys\n Def: Any condition caused by failure of the kidneys to correctly develop during the antenatal period....\n --PARENT--> [?] Structural developmental anomalies of the urinary system\n Def: Any condition caused by failure of the urinary system to correctly develop during the antenatal period....", "[LB30.7] Ectopic or pelvic kidney\n Def: A birth defect characterised by an abnormally positioned kidney; may be asymptomatic or result in urine blockage, infection or kidney stones...\n --PARENT--> [LB30] Structural developmental anomalies of kidneys\n Def: Any condition caused by failure of the kidneys to correctly develop during the antenatal period....\n --CHILD--> [LB30.1] Renal dysplasia\n Def: A condition characterised by abnormal development of one or both kidneys...." ]
FC00.3
Acquired deformity of pelvis
[ { "from_icd11": "FC00.3", "icd10_code": "M955", "icd10_title": "Acquired deformity of pelvis" }, { "from_icd11": "LB30.7", "icd10_code": "Q632", "icd10_title": "Ectopic kidney" }, { "from_icd11": "LB30.7", "icd10_code": "Q63", "icd10_title": "Other congenital malformations of kidney" }, { "from_icd11": "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": "GA05.Z", "icd10_code": "N739", "icd10_title": "Female pelvic inflammatory disease, unspecified" }, { "from_icd11": "GA05.Z", "icd10_code": "N738", "icd10_title": "Other specified female pelvic inflammatory diseases" }, { "from_icd11": "GA05.Z", "icd10_code": "N74", "icd10_title": "Female pelvic inflammatory disorders in diseases classified elsewhere" } ]
M955
Acquired deformity of pelvis
Because the results of biochemical tests indicated renal damage, plain abdominal computed tomography (CT) was performed. An irregular tumor of approximately 130 mm × 120 mm × 80 mm in size was observed in the left upper quadrant, which corresponds to the transverse colon. No intestinal distention was observed on the oral side of the tumor. Moreover, the tumor was in close contact with the pancreatic body and tail, and the gastric corpus greater curvature, suggesting invasion into nearby organs. Also, mildly enlarged lymph nodes were observed at the periphery of the tumor . Fig. 1 Abdominal computed tomography imaging. A plain abdominal computed tomography (CT) image on admission shows an irregular tumor in the left upper quadrant corresponding to the transverse colon. The tumor was in close contact with the pancreatic body and tail, and the gastric corpus greater curvature. Mildly enlarged lymph nodes were observed at the periphery of the tumorous lesion (1 a and 1 b ). The second plain abdominal CT conducted 36 days after the first CT showed that the tumor had regressed spontaneously and the swelling of lymph nodes around the tumorous lesion had disappeared (1 c and 1 d ). CT conducted 48 days after the first visit revealed intestinal distention on the oral side of the narrowed area in the transverse colon, and the patient underwent decompression by transanal ileus tube insertion (1 e and 1 f )
3.849609
0.962402
sec[1]/p[2]
en
0.999997
31931725
https://doi.org/10.1186/s12876-020-1162-2
[ "tumor", "abdominal", "plain", "computed", "tomography", "transverse", "colon", "lymph", "nodes", "irregular" ]
[ { "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": "MD81.3", "title": "Acute abdomen" }, { "code": "JA01.0", "title": "Abdominal pregnancy" }, { "code": "ME04.Z", "title": "Ascites, unspecified" }, { "code": "NB51.0&XA3KX0", "title": "Laceration without foreign body of abdominal wall" }, { "code": "NB9Y", "title": "Other specified injuries to the abdomen, lower back, lumbar spine or pelvis" } ]
=== ICD-11 CODES FOUND === [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 [MD81.3] Acute abdomen Definition: A clinical syndrome with acute abdominal pain that is severe, and rapid onset. Acute abdomen may be caused by a variety of disorders, injuries, or diseases Also known as: Acute abdomen | acute abdominal pain syndrome | surgical abdomen | abdominal acute syndrome | severe abdomen pain [JA01.0] Abdominal pregnancy Definition: A condition characterised by implantation of the embryo within the peritoneal cavity during pregnancy. Also known as: Abdominal pregnancy | abdomen pregnancy | intraperitoneal pregnancy Excludes: Maternal care for viable fetus in abdominal pregnancy | Delivery of viable fetus in abdominal pregnancy [ME04.Z] Ascites, unspecified Also known as: Ascites, unspecified | Ascites | abdominal dropsy | hydrops abdominis | ascites NOS [NB9Y] Other specified injuries to the abdomen, lower back, lumbar spine or pelvis Also known as: Other specified injuries to the abdomen, lower back, lumbar spine or pelvis | Abdominal wall trauma | Injury of pelvic floor | pelvic floor blunt injury | pelvic floor blunt trauma === GRAPH WALKS === --- Walk 1 --- [2F9Z] Neoplasms of unknown behaviour of unspecified site --PARENT--> [?] Neoplasms of unknown behaviour, except of lymphoid, haematopoietic, central nervous system or related tissues --RELATED_TO--> [?] Pathological fracture in neoplastic disease of unknown behaviour --- Walk 2 --- [2F9Z] Neoplasms of unknown behaviour of unspecified site --PARENT--> [?] Neoplasms of unknown behaviour, except of lymphoid, haematopoietic, central nervous system or related tissues --RELATED_TO--> [?] Pathological fracture in neoplastic disease of unknown behaviour --- Walk 3 --- [ME61] Subcutaneous swelling, mass or lump of uncertain or unspecified nature Def: One or more localised subcutaneous soft tissue masses of undetermined or unspecified nature... --PARENT--> [?] Symptoms or signs involving the skin Def: This category allows the capture of imprecise data where a more specific diagnosis cannot be made or to supplement information about a specific diagnosis.... --CHILD--> [ME60] Skin lesion of uncertain or unspecified nature Def: To be used where there is either significant uncertainty or alternatively no information as to the nature of a circumscribed skin lesion. This is of particular importance with regard to whether or not... --- Walk 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--> [?] Benign symmetrical lipomatosis Def: Benign symmetrical lipomatosis is an uncommon condition characterised by progressive symmetrical accumulation during adult life of adipose mass at the level of the head, neck and upper trunk . The con... --- Walk 5 --- [2E6Z] Carcinoma in situ of unspecified site --PARENT--> [?] In situ neoplasms, except of lymphoid, haematopoietic, central nervous system or related tissues --CHILD--> [2E60] Carcinoma in situ of oral cavity, oesophagus or stomach --- Walk 6 --- [2E6Z] Carcinoma in situ of unspecified site --PARENT--> [?] In situ neoplasms, except of lymphoid, haematopoietic, central nervous system or related tissues --CHILD--> [2E60] Carcinoma in situ of oral cavity, oesophagus or stomach
[ "[2F9Z] Neoplasms of unknown behaviour of unspecified site\n --PARENT--> [?] Neoplasms of unknown behaviour, except of lymphoid, haematopoietic, central nervous system or related tissues\n --RELATED_TO--> [?] Pathological fracture in neoplastic disease of unknown behaviour", "[2F9Z] Neoplasms of unknown behaviour of unspecified site\n --PARENT--> [?] Neoplasms of unknown behaviour, except of lymphoid, haematopoietic, central nervous system or related tissues\n --RELATED_TO--> [?] Pathological fracture in neoplastic disease of unknown behaviour", "[ME61] Subcutaneous swelling, mass or lump of uncertain or unspecified nature\n Def: One or more localised subcutaneous soft tissue masses of undetermined or unspecified nature...\n --PARENT--> [?] Symptoms or signs involving the skin\n Def: This category allows the capture of imprecise data where a more specific diagnosis cannot be made or to supplement information about a specific diagnosis....\n --CHILD--> [ME60] Skin lesion of uncertain or unspecified nature\n Def: To be used where there is either significant uncertainty or alternatively no information as to the nature of a circumscribed skin lesion. This is of particular importance with regard to whether or not...", "[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--> [?] Benign symmetrical lipomatosis\n Def: Benign symmetrical lipomatosis is an uncommon condition characterised by progressive symmetrical accumulation during adult life of adipose mass at the level of the head, neck and upper trunk . The con...", "[2E6Z] Carcinoma in situ of unspecified site\n --PARENT--> [?] In situ neoplasms, except of lymphoid, haematopoietic, central nervous system or related tissues\n --CHILD--> [2E60] Carcinoma in situ of oral cavity, oesophagus or stomach", "[2E6Z] Carcinoma in situ of unspecified site\n --PARENT--> [?] In situ neoplasms, except of lymphoid, haematopoietic, central nervous system or related tissues\n --CHILD--> [2E60] Carcinoma in situ of oral cavity, oesophagus or stomach" ]
2F9Z
Neoplasms of unknown behaviour of unspecified site
[ { "from_icd11": "2F9Z", "icd10_code": "D487", "icd10_title": "Neoplasm of uncertain behavior of other specified sites" }, { "from_icd11": "2F9Z", "icd10_code": "D482", "icd10_title": "Neoplasm of uncertain behavior of peripheral nerves and autonomic nervous system" }, { "from_icd11": "2F9Z", "icd10_code": "D37-D48", "icd10_title": "" }, { "from_icd11": "2F9Z", "icd10_code": "D377", "icd10_title": "" }, { "from_icd11": "2F9Z", "icd10_code": "D48", "icd10_title": "Neoplasm of uncertain behavior of other and unspecified sites" }, { "from_icd11": "2F9Z", "icd10_code": "D489", "icd10_title": "Neoplasm of uncertain behavior, unspecified" }, { "from_icd11": "ME61", "icd10_code": "R2240", "icd10_title": "Localized swelling, mass and lump, unspecified lower limb" }, { "from_icd11": "ME61", "icd10_code": "R2232", "icd10_title": "Localized swelling, mass and lump, left upper limb" }, { "from_icd11": "ME61", "icd10_code": "R2242", "icd10_title": "Localized swelling, mass and lump, left lower limb" }, { "from_icd11": "ME61", "icd10_code": "R2231", "icd10_title": "Localized swelling, mass and lump, right upper limb" }, { "from_icd11": "ME61", "icd10_code": "R2241", "icd10_title": "Localized swelling, mass and lump, right lower limb" }, { "from_icd11": "ME61", "icd10_code": "R2233", "icd10_title": "Localized swelling, mass and lump, upper limb, bilateral" }, { "from_icd11": "ME61", "icd10_code": "R2243", "icd10_title": "Localized swelling, mass and lump, lower limb, bilateral" }, { "from_icd11": "ME61", "icd10_code": "R2230", "icd10_title": "Localized swelling, mass and lump, unspecified upper limb" }, { "from_icd11": "ME61", "icd10_code": "R220", "icd10_title": "Localized swelling, mass and lump, head" } ]
D487
Neoplasm of uncertain behavior of other specified sites
The patient's symptomatology was characterized by ictal fear as the first manifestation. The results of scalp EEG indicated that the onset of epileptiform discharge localized in the bilateral posterior head, which was significantly larger in the left occipital, parietal, and posterior temporal areas characterized by the 6–7 Hz oscillation. The clinical symptoms appeared 1.5 s after the EEG onset, while the frontal and temporal electrodes did not have epileptic discharges at the beginning of the clinical seizure. In the later stage, the left fronto-temporal electrodes showed the 3.5–4 Hz oscillation. Therefore, the scalp vEEG results indicated that the seizures may have originated from the left occipital, parietal, and posterior temporal areas. The brain imaging evidences (T2 flair and PET-CT) also suggest the possible pathological changes in the left occipital, parietal, and posterior temporal areas. However, the first manifestation was ictal fear, which is unusual for episodes of seizure originating from posterior brain areas. It is reported that ictal fear is not only associated with the epileptic discharges in the amygdala, but also occur when the anterior cingulate cortex, orbital frontal cortex, and temporal lobes are hyperactive ( 5 ). Under pathological conditions, the inhibition from the amygdala to the OFC is reduced, which causes the release of negative emotions such as fear and anger.
4.261719
0.671875
sec[2]/p[0]
en
0.999997
30131760
https://doi.org/10.3389/fneur.2018.00644
[ "temporal", "fear", "areas", "ictal", "that", "which", "occipital", "parietal", "characterized", "manifestation" ]
[ { "code": "4A44.2", "title": "Giant cell arteritis" }, { "code": "8B82.Z", "title": "Disorders of trigeminal nerve, unspecified" }, { "code": "4A44.Y", "title": "Other specified vasculitis" }, { "code": "NA0Z&XA9T94", "title": "Temporal region injury" }, { "code": "NA01.Z&XA9T94", "title": "Temporal wound" }, { "code": "MB24.A", "title": "Fear" }, { "code": "MG24.Z", "title": "Fear of disease, unspecified" }, { "code": "6B0Z", "title": "Anxiety or fear-related disorders, unspecified" }, { "code": "MG24.Y", "title": "Fear of other specified disease" }, { "code": "6B03", "title": "Specific phobia" } ]
=== ICD-11 CODES FOUND === [4A44.2] Giant cell arteritis Definition: Arteritis, often granulomatous, usually affecting the aorta and/or its major branches, with a predilection for the branches of the carotid artery. Often involves the temporal artery. Onset usually in patients older than 50 and often associated with polymyalgia rheumatica. Also known as: Giant cell arteritis | GCA - [giant cell arteritis] | temporal arteritis | cranial arteritis | Horton disease [8B82.Z] Disorders of trigeminal nerve, unspecified Also known as: Disorders of trigeminal nerve, unspecified | Disorders of trigeminal nerve | Disorders of 5th cranial nerve | disorders of the fifth cranial nerve | Gasserian ganglion lesion [4A44.Y] Other specified vasculitis Also known as: Other specified vasculitis | Large vessel vasculitis | Juvenile temporal arteritis | Medium-sized vessel vasculitis | Polyangiitis overlap syndrome [MB24.A] Fear Definition: An emotional response to perceived imminent threat or danger associated with urges to flee or fight. Also known as: Fear [MG24.Z] Fear of disease, unspecified Also known as: Fear of disease, unspecified | Fear of disease | morbophobia [6B0Z] Anxiety or fear-related disorders, unspecified Also known as: Anxiety or fear-related disorders, unspecified | Phobia NOS | phobic anxiety disorders | phobic disorder | Phobic state NOS [MG24.Y] Fear of other specified disease Also known as: Fear of other specified disease | Fear of sexual dysfunction male [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 === GRAPH WALKS === --- Walk 1 --- [4A44.2] Giant cell arteritis Def: Arteritis, often granulomatous, usually affecting the aorta and/or its major branches, with a predilection for the branches of the carotid artery. Often involves the temporal artery. Onset usually in ... --PARENT--> [4A44] Vasculitis Def: Vasculitides represent a heterogenous group of diseases of multifactorial aetiology characterised by inflammatory lesions of vessels. These lesions consist of fibrinoid necrosis (necrotizing arteritis... --CHILD--> [4A44.0] Rhizomelic pseudopolyarthritis --- Walk 2 --- [4A44.2] Giant cell arteritis Def: Arteritis, often granulomatous, usually affecting the aorta and/or its major branches, with a predilection for the branches of the carotid artery. Often involves the temporal artery. Onset usually in ... --PARENT--> [4A44] Vasculitis Def: Vasculitides represent a heterogenous group of diseases of multifactorial aetiology characterised by inflammatory lesions of vessels. These lesions consist of fibrinoid necrosis (necrotizing arteritis... --CHILD--> [4A44.2] Giant cell arteritis Def: Arteritis, often granulomatous, usually affecting the aorta and/or its major branches, with a predilection for the branches of the carotid artery. Often involves the temporal artery. Onset usually in ... --- Walk 3 --- [8B82.Z] Disorders of trigeminal nerve, unspecified --PARENT--> [8B82] Disorders of trigeminal nerve Def: The trigeminal nerve is a mixed nerve with three divisions, ophthalmic, maxillary and mandibular divisions, that provides sensory innervation to the face and mucous membrane of the oral and nasal cavi... --CHILD--> [8B82.Z] Disorders of trigeminal nerve, unspecified --- Walk 4 --- [8B82.Z] Disorders of trigeminal nerve, unspecified --PARENT--> [8B82] Disorders of trigeminal nerve Def: The trigeminal nerve is a mixed nerve with three divisions, ophthalmic, maxillary and mandibular divisions, that provides sensory innervation to the face and mucous membrane of the oral and nasal cavi... --RELATED_TO--> [?] Atypical facial pain Def: This is a chronic pain of the face, which does not meet other diagnostic criteria.... --- Walk 5 --- [4A44.Y] Other specified vasculitis --PARENT--> [4A44] Vasculitis Def: Vasculitides represent a heterogenous group of diseases of multifactorial aetiology characterised by inflammatory lesions of vessels. These lesions consist of fibrinoid necrosis (necrotizing arteritis... --CHILD--> [4A44.2] Giant cell arteritis Def: Arteritis, often granulomatous, usually affecting the aorta and/or its major branches, with a predilection for the branches of the carotid artery. Often involves the temporal artery. Onset usually in ... --- Walk 6 --- [4A44.Y] Other specified vasculitis --PARENT--> [4A44] Vasculitis Def: Vasculitides represent a heterogenous group of diseases of multifactorial aetiology characterised by inflammatory lesions of vessels. These lesions consist of fibrinoid necrosis (necrotizing arteritis... --RELATED_TO--> [?] Behçet disease Def: Behçet disease is a disease of incompletely understood aetiopathogenesis characterised by recurrent oral and/or genital aphthous ulcers accompanied by cutaneous, ocular, articular, gastrointestinal, a...
[ "[4A44.2] Giant cell arteritis\n Def: Arteritis, often granulomatous, usually affecting the aorta and/or its major branches, with a predilection for the branches of the carotid artery. Often involves the temporal artery. Onset usually in ...\n --PARENT--> [4A44] Vasculitis\n Def: Vasculitides represent a heterogenous group of diseases of multifactorial aetiology characterised by inflammatory lesions of vessels. These lesions consist of fibrinoid necrosis (necrotizing arteritis...\n --CHILD--> [4A44.0] Rhizomelic pseudopolyarthritis", "[4A44.2] Giant cell arteritis\n Def: Arteritis, often granulomatous, usually affecting the aorta and/or its major branches, with a predilection for the branches of the carotid artery. Often involves the temporal artery. Onset usually in ...\n --PARENT--> [4A44] Vasculitis\n Def: Vasculitides represent a heterogenous group of diseases of multifactorial aetiology characterised by inflammatory lesions of vessels. These lesions consist of fibrinoid necrosis (necrotizing arteritis...\n --CHILD--> [4A44.2] Giant cell arteritis\n Def: Arteritis, often granulomatous, usually affecting the aorta and/or its major branches, with a predilection for the branches of the carotid artery. Often involves the temporal artery. Onset usually in ...", "[8B82.Z] Disorders of trigeminal nerve, unspecified\n --PARENT--> [8B82] Disorders of trigeminal nerve\n Def: The trigeminal nerve is a mixed nerve with three divisions, ophthalmic, maxillary and mandibular divisions, that provides sensory innervation to the face and mucous membrane of the oral and nasal cavi...\n --CHILD--> [8B82.Z] Disorders of trigeminal nerve, unspecified", "[8B82.Z] Disorders of trigeminal nerve, unspecified\n --PARENT--> [8B82] Disorders of trigeminal nerve\n Def: The trigeminal nerve is a mixed nerve with three divisions, ophthalmic, maxillary and mandibular divisions, that provides sensory innervation to the face and mucous membrane of the oral and nasal cavi...\n --RELATED_TO--> [?] Atypical facial pain\n Def: This is a chronic pain of the face, which does not meet other diagnostic criteria....", "[4A44.Y] Other specified vasculitis\n --PARENT--> [4A44] Vasculitis\n Def: Vasculitides represent a heterogenous group of diseases of multifactorial aetiology characterised by inflammatory lesions of vessels. These lesions consist of fibrinoid necrosis (necrotizing arteritis...\n --CHILD--> [4A44.2] Giant cell arteritis\n Def: Arteritis, often granulomatous, usually affecting the aorta and/or its major branches, with a predilection for the branches of the carotid artery. Often involves the temporal artery. Onset usually in ...", "[4A44.Y] Other specified vasculitis\n --PARENT--> [4A44] Vasculitis\n Def: Vasculitides represent a heterogenous group of diseases of multifactorial aetiology characterised by inflammatory lesions of vessels. These lesions consist of fibrinoid necrosis (necrotizing arteritis...\n --RELATED_TO--> [?] Behçet disease\n Def: Behçet disease is a disease of incompletely understood aetiopathogenesis characterised by recurrent oral and/or genital aphthous ulcers accompanied by cutaneous, ocular, articular, gastrointestinal, a..." ]
4A44.2
Giant cell arteritis
[ { "from_icd11": "4A44.2", "icd10_code": "M316", "icd10_title": "Other giant cell arteritis" }, { "from_icd11": "8B82.Z", "icd10_code": "G508", "icd10_title": "Other disorders of trigeminal nerve" }, { "from_icd11": "8B82.Z", "icd10_code": "G509", "icd10_title": "Disorder of trigeminal nerve, unspecified" }, { "from_icd11": "8B82.Z", "icd10_code": "G50", "icd10_title": "Disorders of trigeminal nerve" }, { "from_icd11": "MG24.Z", "icd10_code": "R45850", "icd10_title": "Homicidal ideations" }, { "from_icd11": "MG24.Z", "icd10_code": "R4584", "icd10_title": "Anhedonia" }, { "from_icd11": "MG24.Z", "icd10_code": "R4587", "icd10_title": "Impulsiveness" }, { "from_icd11": "MG24.Z", "icd10_code": "R4586", "icd10_title": "Emotional lability" }, { "from_icd11": "MG24.Z", "icd10_code": "R4581", "icd10_title": "Low self-esteem" }, { "from_icd11": "MG24.Z", "icd10_code": "R4589", "icd10_title": "Other symptoms and signs involving emotional state" }, { "from_icd11": "MG24.Z", "icd10_code": "R4583", "icd10_title": "Excessive crying of child, adolescent or adult" }, { "from_icd11": "MG24.Z", "icd10_code": "R458", "icd10_title": "Other symptoms and signs involving emotional state" }, { "from_icd11": "6B0Z", "icd10_code": "F419", "icd10_title": "Anxiety disorder, unspecified" }, { "from_icd11": "6B0Z", "icd10_code": "F409", "icd10_title": "Phobic anxiety disorder, unspecified" }, { "from_icd11": "6B0Z", "icd10_code": "F408", "icd10_title": "Other phobic anxiety disorders" } ]
M316
Other giant cell arteritis
His MRI showed an abnormal symmetrical signal in the bilateral basal ganglia, which was considered to be indicative of DEACMP . Of note, the bilateral cerebral peduncles also showed abnormal symmetrical signals . The patient’s EEG indicated that Fp1, Fp2, F4, F8 leads in the frontal lobe area had a mixture of wide sharp, sharp, and three-phase waves . Based on the above clinical manifestations and examination results, the patient was diagnosed with DEACMP. We recommend that the patient be treated with hyperbaric oxygen therapy (HBO). The relatives decided to return the patient to the local hospital to continue rehabilitation. At hospital discharge, the patient had blurred consciousness, indifferent expression, poor understanding, poor memory, poor orientation of characters and space, slow response, and low speech. His tongue was slightly to the right. Proximity muscle strength of right lower limb was grade 4+, and distal muscle strength was grade 3-. Fig. 1 A bilateral symmetrical anomaly signal of the basal ganglia was captured in fluid attenuated inversion recovery images ( a ). Bilateral cerebral peduncles showed symmetrical high signals in DWI ( b ), but low signals in ADC Fig. 2 The EEG indicated a diffuse distribution of Delta waves. The Fp1, Fp2, F4 in the frontal lobe area had a mixture of wide sharp, sharp, and three-phase waves. No clinical events occurred during the monitoring process
3.914063
0.979004
sec[1]/sec[0]/p[3]
en
0.999997
32183727
https://doi.org/10.1186/s12883-020-01677-5
[ "symmetrical", "sharp", "signals", "waves", "poor", "signal", "basal", "ganglia", "deacmp", "cerebral" ]
[ { "code": "KA20.11", "title": "Symmetrical intrauterine growth restriction" }, { "code": "EC23.Y", "title": "Other specified genetic disorders of skin pigmentation" }, { "code": "EF02.1", "title": "Subcutaneous lipomatosis" }, { "code": "KA20.00", "title": "Small for gestational age, symmetrical" }, { "code": "EK5Y", "title": "Other specified skin disorders provoked by external factors" }, { "code": "4A43.3", "title": "Mixed connective tissue disease" }, { "code": "PA83.1", "title": "Unintentionally cut or pierced by sharp glass" }, { "code": "PG9Z&XE4BU", "title": "Contact with sharp object, undetermined intent" }, { "code": "PG9Z", "title": "Cut or pierced by other or unspecified sharp object, undetermined intent" }, { "code": "PE3Z", "title": "Assault by being cut or pierced by other or unspecified sharp object" } ]
=== ICD-11 CODES FOUND === [KA20.11] Symmetrical intrauterine growth restriction Definition: This condition begins earlier in pregnancy and there is a higher incidence of permanent neurologic sequela. It is often associated with either genetic abnormalities or fetal infection, especially 1st trimester viral infections. Also known as: Symmetrical intrauterine growth restriction | Symmetrical IUGR | symmetrical growth retardation [EC23.Y] Other specified genetic disorders of skin pigmentation Also known as: Other specified genetic disorders of skin pigmentation | Genetically-determined mixed hyper- and hypomelanotic disorders of skin pigmentation | Hereditary universal dyschromatosis | Dyschromatosis universalis hereditaria | DUH1 - [Dyschromatosis universalis hereditaria] (MIM 127500) [EF02.1] Subcutaneous lipomatosis Definition: Diffuse infiltration of the subcutis by non-encapsulated adipose tissue. Also known as: Subcutaneous lipomatosis | Benign symmetrical lipomatosis | Launois-Bensaude adenolipomatosis | Central non-encapsulated lipomatosis | Madelung disease Includes: Lipomatosis dolorosa [KA20.00] Small for gestational age, symmetrical Definition: Growth of the fetus is affected in early pregnancy and growth is slow throughout the duration of the pregnancy. The head circumference is proportional to the rest of the body. Birth weight is 2 standard deviations below the mean, or below the 10th percentile. Also known as: Small for gestational age, symmetrical [EK5Y] Other specified skin disorders provoked by external factors Also known as: Other specified skin disorders provoked by external factors | Dermatoses provoked by physical or environmental factors | Piezogenic pedal papules | Occupational callosities | Interdigital pilonidal sinus [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 [PA83.1] Unintentionally cut or pierced by sharp glass Also known as: Unintentionally cut or pierced by sharp glass | contact with sharp glass causing accidental injury | contact with sharp glass [PG9Z] Cut or pierced by other or unspecified sharp object, undetermined intent Also known as: Cut or pierced by other or unspecified sharp object, undetermined intent | multiple sharp force injuries | Contact with sharp object, undetermined intent [PE3Z] Assault by being cut or pierced by other or unspecified sharp object Also known as: Assault by being cut or pierced by other or unspecified sharp object | assault by sharp object | assault by being stabbed NOS | stabbed NOS | stabbed by another === GRAPH WALKS === --- Walk 1 --- [KA20.11] Symmetrical intrauterine growth restriction Def: This condition begins earlier in pregnancy and there is a higher incidence of permanent neurologic sequela. It is often associated with either genetic abnormalities or fetal infection, especially 1st ... --PARENT--> [KA20.1] Intrauterine growth restriction Def: The fetus does not achieve its predicted genetic potential and infant, not light or small for gestational age, showing signs of fetal malnutrition.... --CHILD--> [KA20.11] Symmetrical intrauterine growth restriction Def: This condition begins earlier in pregnancy and there is a higher incidence of permanent neurologic sequela. It is often associated with either genetic abnormalities or fetal infection, especially 1st ... --- Walk 2 --- [KA20.11] Symmetrical intrauterine growth restriction Def: This condition begins earlier in pregnancy and there is a higher incidence of permanent neurologic sequela. It is often associated with either genetic abnormalities or fetal infection, especially 1st ... --PARENT--> [KA20.1] Intrauterine growth restriction Def: The fetus does not achieve its predicted genetic potential and infant, not light or small for gestational age, showing signs of fetal malnutrition.... --CHILD--> [KA20.12] Intrauterine growth restriction associated with small for gestational age Def: These infants are classified as small for gestational age but have also been subject to intrauterine growth restriction.... --- Walk 3 --- [EC23.Y] Other specified genetic disorders of skin pigmentation --PARENT--> [EC23] Genetic disorders of skin pigmentation Def: Genetic disorders of the skin characterised by disordered pigmentation, including albinism and inherited forms of lentiginosis.... --CHILD--> [EC23.2] Albinism or other specified genetically-determined hypomelanotic disorders Def: A large group of heritable disorders in which cutaneous melanin production is reduced or absent, mainly as the result of defects in enzymes required for normal melanin biosynthesis.... --- Walk 4 --- [EC23.Y] Other specified genetic disorders of skin pigmentation --PARENT--> [EC23] Genetic disorders of skin pigmentation Def: Genetic disorders of the skin characterised by disordered pigmentation, including albinism and inherited forms of lentiginosis.... --CHILD--> [EC23.2] Albinism or other specified genetically-determined hypomelanotic disorders Def: A large group of heritable disorders in which cutaneous melanin production is reduced or absent, mainly as the result of defects in enzymes required for normal melanin biosynthesis.... --- Walk 5 --- [EF02.1] Subcutaneous lipomatosis Def: Diffuse infiltration of the subcutis by non-encapsulated adipose tissue.... --PARENT--> [EF02] Certain noninflammatory disorders of subcutaneous fat --CHILD--> [EF02.0] Fat hypertrophy Def: Focal hypertrophy of subcutaneous adipose tissue. It is a common sequela of long-term insulin injection into the skin.... --- Walk 6 --- [EF02.1] Subcutaneous lipomatosis Def: Diffuse infiltration of the subcutis by non-encapsulated adipose tissue.... --PARENT--> [EF02] Certain noninflammatory disorders of subcutaneous fat --CHILD--> [EF02.1] Subcutaneous lipomatosis Def: Diffuse infiltration of the subcutis by non-encapsulated adipose tissue....
[ "[KA20.11] Symmetrical intrauterine growth restriction\n Def: This condition begins earlier in pregnancy and there is a higher incidence of permanent neurologic sequela. It is often associated with either genetic abnormalities or fetal infection, especially 1st ...\n --PARENT--> [KA20.1] Intrauterine growth restriction\n Def: The fetus does not achieve its predicted genetic potential and infant, not light or small for gestational age, showing signs of fetal malnutrition....\n --CHILD--> [KA20.11] Symmetrical intrauterine growth restriction\n Def: This condition begins earlier in pregnancy and there is a higher incidence of permanent neurologic sequela. It is often associated with either genetic abnormalities or fetal infection, especially 1st ...", "[KA20.11] Symmetrical intrauterine growth restriction\n Def: This condition begins earlier in pregnancy and there is a higher incidence of permanent neurologic sequela. It is often associated with either genetic abnormalities or fetal infection, especially 1st ...\n --PARENT--> [KA20.1] Intrauterine growth restriction\n Def: The fetus does not achieve its predicted genetic potential and infant, not light or small for gestational age, showing signs of fetal malnutrition....\n --CHILD--> [KA20.12] Intrauterine growth restriction associated with small for gestational age\n Def: These infants are classified as small for gestational age but have also been subject to intrauterine growth restriction....", "[EC23.Y] Other specified genetic disorders of skin pigmentation\n --PARENT--> [EC23] Genetic disorders of skin pigmentation\n Def: Genetic disorders of the skin characterised by disordered pigmentation, including albinism and inherited forms of lentiginosis....\n --CHILD--> [EC23.2] Albinism or other specified genetically-determined hypomelanotic disorders\n Def: A large group of heritable disorders in which cutaneous melanin production is reduced or absent, mainly as the result of defects in enzymes required for normal melanin biosynthesis....", "[EC23.Y] Other specified genetic disorders of skin pigmentation\n --PARENT--> [EC23] Genetic disorders of skin pigmentation\n Def: Genetic disorders of the skin characterised by disordered pigmentation, including albinism and inherited forms of lentiginosis....\n --CHILD--> [EC23.2] Albinism or other specified genetically-determined hypomelanotic disorders\n Def: A large group of heritable disorders in which cutaneous melanin production is reduced or absent, mainly as the result of defects in enzymes required for normal melanin biosynthesis....", "[EF02.1] Subcutaneous lipomatosis\n Def: Diffuse infiltration of the subcutis by non-encapsulated adipose tissue....\n --PARENT--> [EF02] Certain noninflammatory disorders of subcutaneous fat\n --CHILD--> [EF02.0] Fat hypertrophy\n Def: Focal hypertrophy of subcutaneous adipose tissue. It is a common sequela of long-term insulin injection into the skin....", "[EF02.1] Subcutaneous lipomatosis\n Def: Diffuse infiltration of the subcutis by non-encapsulated adipose tissue....\n --PARENT--> [EF02] Certain noninflammatory disorders of subcutaneous fat\n --CHILD--> [EF02.1] Subcutaneous lipomatosis\n Def: Diffuse infiltration of the subcutis by non-encapsulated adipose tissue...." ]
KA20.11
Symmetrical intrauterine growth restriction
[ { "from_icd11": "EF02.1", "icd10_code": "L988", "icd10_title": "Other specified disorders of the skin and subcutaneous tissue" }, { "from_icd11": "EF02.1", "icd10_code": "E882", "icd10_title": "Lipomatosis, not elsewhere classified" }, { "from_icd11": "EK5Y", "icd10_code": "L259", "icd10_title": "Unspecified contact dermatitis, unspecified cause" }, { "from_icd11": "4A43.3", "icd10_code": "M351", "icd10_title": "Other overlap syndromes" }, { "from_icd11": "4A43.3", "icd10_code": "M35", "icd10_title": "Other systemic involvement of connective tissue" }, { "from_icd11": "PA83.1", "icd10_code": "W25XXXA", "icd10_title": "Contact with sharp glass, initial encounter" }, { "from_icd11": "PA83.1", "icd10_code": "W25XXXS", "icd10_title": "Contact with sharp glass, sequela" }, { "from_icd11": "PA83.1", "icd10_code": "W25XXXD", "icd10_title": "Contact with sharp glass, subsequent encounter" }, { "from_icd11": "PA83.1", "icd10_code": "W25", "icd10_title": "Contact with sharp glass" }, { "from_icd11": "PG9Z&XE4BU", "icd10_code": "Y288XXA", "icd10_title": "Contact with other sharp object, undetermined intent, initial encounter" }, { "from_icd11": "PG9Z&XE4BU", "icd10_code": "Y281XXA", "icd10_title": "Contact with knife, undetermined intent, initial encounter" }, { "from_icd11": "PG9Z&XE4BU", "icd10_code": "Y289XXA", "icd10_title": "Contact with unspecified sharp object, undetermined intent, initial encounter" }, { "from_icd11": "PG9Z&XE4BU", "icd10_code": "Y281XXD", "icd10_title": "Contact with knife, undetermined intent, subsequent encounter" }, { "from_icd11": "PG9Z&XE4BU", "icd10_code": "Y28", "icd10_title": "Contact with sharp object, undetermined intent" }, { "from_icd11": "PE3Z", "icd10_code": "X999XXA", "icd10_title": "Assault by unspecified sharp object, initial encounter" } ]
L988
Other specified disorders of the skin and subcutaneous tissue
A 68-year-old Caucasian man was referred to our out-patients clinic following the incidental discovery of a 6 × 8 cm distended iliac vessel whilst having an ultrasound for surveillance of liver cirrhosis. His clinical history revealed a progressive history of right flank pain, worsening right leg claudication and a persistently cold sensation in his right foot. He also complained of progressive breathlessness on exertion, clinically suggestive of deteriorating CCF. There was no history of trauma or previous surgery. Ankle-brachial pressure measurements revealed a reduced index of 0.76 on the right, and a normal index of 1.35 on the left with corresponding toe pressures of 55 mmHg and 143 mmHg respectively. A contrast enhanced computed tomography (CT) scan showed an isolated right common iliac artery (CIA) to right common iliac vein AVF . His aorta was normal in caliber, measuring 19 mm at the aortic bifurcation. The aneurysmal segment began immediately distal to the aortic bifurcation at the origin of the right CIA, with no normal segment of CIA evident. The aneurysm measured 9.4 cm in maximal diameter and extended to within 17 mm of the right iliac bifurcation. It was impossible to differentiate the arterial wall from the venous wall in the aneurysmal segment on either ultrasound or CT scans. His inferior vena cava (IVC) was grossly distended with a uniform diameter of 36 mm in its full course.
4.007813
0.978027
sec[0]/sec[0]/p[0]
en
0.999998
21859469
https://doi.org/10.1186/1752-1947-5-401
[ "iliac", "bifurcation", "segment", "distended", "ultrasound", "index", "mmhg", "common", "aortic", "aneurysmal" ]
[ { "code": "BD30.10&XA83D6", "title": "Acute thromboembolic iliac artery occlusion" }, { "code": "BD30.11&XA83D6", "title": "Acute thrombotic iliac artery occlusion" }, { "code": "NB90.6Y&XA83D6", "title": "Iliac artery haematoma" }, { "code": "BD52.3", "title": "Rupture of artery" }, { "code": "NB53.6", "title": "Strain or sprain of sacroiliac joint" }, { "code": "LB73.11", "title": "Bifid rib" }, { "code": "BD40.3", "title": "Aortic bifurcation syndrome" }, { "code": "BD30.10", "title": "Acute thromboembolic aortoiliac occlusion" }, { "code": "BD30.11", "title": "Acute thrombotic aortoiliac occlusion" }, { "code": "BD30.1Y", "title": "Other specified acute aortoiliac occlusion" } ]
=== ICD-11 CODES FOUND === [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 [NB53.6] Strain or sprain of sacroiliac joint Definition: Aberrant biomechanical functions of the joints between the ilia and the sacrum, which may be as a result of local disease, systemic disease, postural strain or trauma. Also known as: Strain or sprain of sacroiliac joint | Innominate sprain of sacral junction | Innominate strain of sacral junction | Strain of sacroiliac joint | sacroiliac sprain [LB73.11] Bifid rib Also known as: Bifid rib | rib bifurcation [BD40.3] Aortic bifurcation syndrome Also known as: Aortic bifurcation syndrome [BD30.10] Acute thromboembolic aortoiliac occlusion Also known as: Acute thromboembolic aortoiliac occlusion | Aortoiliac arterial embolism | Acute thromboembolic visceral artery occlusion | Coeliac artery embolism | Acute thromboembolic aortic bifurcation occlusion [BD30.11] Acute thrombotic aortoiliac occlusion Also known as: Acute thrombotic aortoiliac occlusion | Acute aortoiliac artery thrombosis | Acute thrombotic visceral artery occlusion | Coeliac artery thrombosis | Acute thrombotic aortic bifurcation occlusion [BD30.1Y] Other specified acute aortoiliac occlusion Also known as: Other specified acute aortoiliac occlusion | Acute visceral artery occlusion | Acute renal artery occlusion | Acute aortic bifurcation occlusion | Acute iliac artery occlusion === GRAPH WALKS === --- Walk 1 --- [BD52.3] Rupture of artery --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... --CHILD--> [?] Injuries to the head --- Walk 2 --- [BD52.3] Rupture of artery --PARENT--> [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... --- Walk 3 --- [NB53.6] Strain or sprain of sacroiliac joint Def: Aberrant biomechanical functions of the joints between the ilia and the sacrum, which may be as a result of local disease, systemic disease, postural strain or trauma.... --PARENT--> [NB53] Dislocation or strain or sprain of joints or ligaments of lumbar spine or pelvis --EXCLUDES--> [?] Dislocation or strain or sprain of joint or ligaments of hip Def: A collective term for muscle and ligament injuries of the tissues associated with, or displacement of the bones of, the hip.... --- Walk 4 --- [NB53.6] Strain or sprain of sacroiliac joint Def: Aberrant biomechanical functions of the joints between the ilia and the sacrum, which may be as a result of local disease, systemic disease, postural strain or trauma.... --PARENT--> [NB53] Dislocation or strain or sprain of joints or ligaments of lumbar spine or pelvis --CHILD--> [NB53.0] Traumatic rupture of lumbar intervertebral disc
[ "[BD52.3] Rupture of artery\n --EXCLUDES--> [?] Injury, poisoning or certain other consequences of external causes\n Def: !markdown\nIn the ICD, injury means physical or physiological bodily harm resulting from interaction of the body with energy (mechanical, thermal, electrical, chemical or radiant, or due to extreme pre...\n --CHILD--> [?] Injuries to the head", "[BD52.3] Rupture of artery\n --PARENT--> [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...", "[NB53.6] Strain or sprain of sacroiliac joint\n Def: Aberrant biomechanical functions of the joints between the ilia and the sacrum, which may be as a result of local disease, systemic disease, postural strain or trauma....\n --PARENT--> [NB53] Dislocation or strain or sprain of joints or ligaments of lumbar spine or pelvis\n --EXCLUDES--> [?] Dislocation or strain or sprain of joint or ligaments of hip\n Def: A collective term for muscle and ligament injuries of the tissues associated with, or displacement of the bones of, the hip....", "[NB53.6] Strain or sprain of sacroiliac joint\n Def: Aberrant biomechanical functions of the joints between the ilia and the sacrum, which may be as a result of local disease, systemic disease, postural strain or trauma....\n --PARENT--> [NB53] Dislocation or strain or sprain of joints or ligaments of lumbar spine or pelvis\n --CHILD--> [NB53.0] Traumatic rupture of lumbar intervertebral disc" ]
BD30.10&XA83D6
Acute thromboembolic iliac artery occlusion
[ { "from_icd11": "BD52.3", "icd10_code": "I772", "icd10_title": "Rupture of artery" }, { "from_icd11": "NB53.6", "icd10_code": "S336XXA", "icd10_title": "Sprain of sacroiliac joint, initial encounter" }, { "from_icd11": "NB53.6", "icd10_code": "S336", "icd10_title": "Sprain of sacroiliac joint" }, { "from_icd11": "BD30.10", "icd10_code": "I7409", "icd10_title": "Other arterial embolism and thrombosis of abdominal aorta" }, { "from_icd11": "BD30.10", "icd10_code": "I7419", "icd10_title": "Embolism and thrombosis of other parts of aorta" }, { "from_icd11": "BD30.10", "icd10_code": "I7411", "icd10_title": "Embolism and thrombosis of thoracic aorta" }, { "from_icd11": "BD30.10", "icd10_code": "I7410", "icd10_title": "Embolism and thrombosis of unspecified parts of aorta" }, { "from_icd11": "BD30.10", "icd10_code": "I7401", "icd10_title": "Saddle embolus of abdominal aorta" }, { "from_icd11": "BD30.10", "icd10_code": "I740", "icd10_title": "Embolism and thrombosis of abdominal aorta" }, { "from_icd11": "BD30.10", "icd10_code": "I741", "icd10_title": "Embolism and thrombosis of other and unspecified parts of aorta" } ]
I772
Rupture of artery
The patient developed a general rash, myalgia, headache, and toothache while working on the demolition project and attributed the symptoms to the common cold. After completing the demolition project in mid-April, he developed tingling in the right foot and formication, and an exacerbation of his headache and toothache. The skin rash repeatedly appeared and disappeared. Following a diagnosis of potential heavy metal poisoning, made at a clinic of oriental medicine, the patient visited a university hospital for heavy metal testing. The results confirmed high levels of mercury, with a blood mercury levels of 16.386 μg/L and a urinary mercury levels of 161.775 μg/L, 2 months following cessation of exposure to mercury. Despite symptomatic treatment, including vitamins, non-steroidal anti-inflammatory drugs (NSAIDs), neuropathic pain relievers, and nerve block, the insomnia and tremor deteriorated, and the patient developed hypesthesia and palsy in the hands. Proteinuria was confirmed by a urine test. Five months after mercury exposure, the patient was transferred to a large general hospital in Seoul to undergo digital infrared thermal imaging (DITI) and a bone scan. Both tests showed no abnormal findings, but the pain persisted. He underwent a nerve block at a pain clinic, but the symptoms worsened, progressing to weakness of muscles, pain, and paresthesia in the lower limbs that hindered ambulation.
3.882813
0.982422
sec[1]/sec[2]/sec[6]/p[0]
en
0.999996
28649389
https://doi.org/10.1186/s40557-017-0184-x
[ "mercury", "pain", "general", "rash", "headache", "toothache", "demolition", "project", "heavy", "metal" ]
[ { "code": "NE61", "title": "Harmful effects of or exposure to noxious substances, chiefly nonmedicinal as to source, not elsewhere classified" }, { "code": "LD2F.0Y", "title": "Other specified toxic or drug-related embryofetopathies" }, { "code": "PB36&XM1FG4", "title": "Unintentional exposure to or harmful effects of mercury or its compounds" }, { "code": "8D43.0Y&XM5DJ5", "title": "Encephalopathy due to methylmercury ingestion" }, { "code": "PD05&XM1FG4", "title": "Intentional self-harm by exposure to or harmful effects of mercury or its compounds" }, { "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 === [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 [LD2F.0Y] Other specified toxic or drug-related embryofetopathies Also known as: Other specified toxic or drug-related embryofetopathies | Acitretin embryofetopathy | Aminopterin embryofetopathy | Cocaine embryofetopathy | Fetal isotretinoin syndrome [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 --- [NE61] Harmful effects of or exposure to noxious substances, chiefly nonmedicinal as to source, not elsewhere classified --EXCLUDES--> [?] Bacterial foodborne intoxications Def: Any condition caused by an intoxication due to a bacterial toxin. Intoxication is by ingestion of contaminated food.... --CHILD--> [?] Foodborne staphylococcal intoxication --- Walk 2 --- [NE61] Harmful effects of or exposure to noxious substances, chiefly nonmedicinal as to source, not elsewhere classified --EXCLUDES--> [?] Bacterial foodborne intoxications Def: Any condition caused by an intoxication due to a bacterial toxin. Intoxication is by ingestion of contaminated food.... --CHILD--> [?] Foodborne Clostridium perfringens intoxication --- Walk 3 --- [LD2F.0Y] Other specified toxic or drug-related embryofetopathies --PARENT--> [LD2F.0] Toxic or drug-related embryofetopathies --CHILD--> [LD2F.00] Fetal alcohol syndrome Def: Fetal alcohol syndrome is a malformation syndrome caused by maternal consumption of alcohol during pregnancy. It is characterised by prenatal and/or postnatal growth deficiency (weight and/or height <... --- Walk 4 --- [LD2F.0Y] Other specified toxic or drug-related embryofetopathies --PARENT--> [LD2F.0] Toxic or drug-related embryofetopathies --CHILD--> [LD2F.00] Fetal alcohol syndrome Def: Fetal alcohol syndrome is a malformation syndrome caused by maternal consumption of alcohol during pregnancy. It is characterised by prenatal and/or postnatal growth deficiency (weight and/or height <...
[ "[NE61] Harmful effects of or exposure to noxious substances, chiefly nonmedicinal as to source, not elsewhere classified\n --EXCLUDES--> [?] Bacterial foodborne intoxications\n Def: Any condition caused by an intoxication due to a bacterial toxin. Intoxication is by ingestion of contaminated food....\n --CHILD--> [?] Foodborne staphylococcal intoxication", "[NE61] Harmful effects of or exposure to noxious substances, chiefly nonmedicinal as to source, not elsewhere classified\n --EXCLUDES--> [?] Bacterial foodborne intoxications\n Def: Any condition caused by an intoxication due to a bacterial toxin. Intoxication is by ingestion of contaminated food....\n --CHILD--> [?] Foodborne Clostridium perfringens intoxication", "[LD2F.0Y] Other specified toxic or drug-related embryofetopathies\n --PARENT--> [LD2F.0] Toxic or drug-related embryofetopathies\n --CHILD--> [LD2F.00] Fetal alcohol syndrome\n Def: Fetal alcohol syndrome is a malformation syndrome caused by maternal consumption of alcohol during pregnancy. It is characterised by prenatal and/or postnatal growth deficiency (weight and/or height <...", "[LD2F.0Y] Other specified toxic or drug-related embryofetopathies\n --PARENT--> [LD2F.0] Toxic or drug-related embryofetopathies\n --CHILD--> [LD2F.00] Fetal alcohol syndrome\n Def: Fetal alcohol syndrome is a malformation syndrome caused by maternal consumption of alcohol during pregnancy. It is characterised by prenatal and/or postnatal growth deficiency (weight and/or height <..." ]
NE61
Harmful effects of or exposure to noxious substances, chiefly nonmedicinal as to source, not elsewhere classified
[ { "from_icd11": "NE61", "icd10_code": "T5802XA", "icd10_title": "Toxic effect of carbon monoxide from motor vehicle exhaust, intentional self-harm, initial encounter" }, { "from_icd11": "NE61", "icd10_code": "T550X2A", "icd10_title": "Toxic effect of soaps, intentional self-harm, initial encounter" }, { "from_icd11": "NE61", "icd10_code": "T61781A", "icd10_title": "Other shellfish poisoning, accidental (unintentional), initial encounter" }, { "from_icd11": "NE61", "icd10_code": "T551X2A", "icd10_title": "Toxic effect of detergents, intentional self-harm, initial encounter" }, { "from_icd11": "NE61", "icd10_code": "T5891XA", "icd10_title": "Toxic effect of carbon monoxide from unspecified source, accidental (unintentional), initial encounter" }, { "from_icd11": "NE61", "icd10_code": "T63711A", "icd10_title": "Toxic effect of contact with venomous marine plant, accidental (unintentional), initial encounter" }, { "from_icd11": "NE61", "icd10_code": "T63712A", "icd10_title": "Toxic effect of contact with venomous marine plant, intentional self-harm, initial encounter" }, { "from_icd11": "NE61", "icd10_code": "T63713A", "icd10_title": "Toxic effect of contact with venomous marine plant, assault, initial encounter" }, { "from_icd11": "NE61", "icd10_code": "T63714A", "icd10_title": "Toxic effect of contact with venomous marine plant, undetermined, initial encounter" }, { "from_icd11": "NE61", "icd10_code": "T63791A", "icd10_title": "Toxic effect of contact with other venomous plant, accidental (unintentional), initial encounter" }, { "from_icd11": "NE61", "icd10_code": "T63792A", "icd10_title": "Toxic effect of contact with other venomous plant, intentional self-harm, initial encounter" }, { "from_icd11": "NE61", "icd10_code": "T63793A", "icd10_title": "Toxic effect of contact with other venomous plant, assault, initial encounter" }, { "from_icd11": "NE61", "icd10_code": "T63794A", "icd10_title": "Toxic effect of contact with other venomous plant, undetermined, initial encounter" }, { "from_icd11": "NE61", "icd10_code": "T61771A", "icd10_title": "Other fish poisoning, accidental (unintentional), initial encounter" }, { "from_icd11": "NE61", "icd10_code": "T61772A", "icd10_title": "Other fish poisoning, intentional self-harm, initial encounter" } ]
T5802XA
Toxic effect of carbon monoxide from motor vehicle exhaust, intentional self-harm, initial encounter
A 18-year-old female reported with a chief complaint of retained milk teeth in upper and lower front region. On extraoral examination, the profile of patient was convex with normal interlabial gap . On intraoral examination, she presented with end-on molar relationship on right and left side, with unerupted maxillary canines and mandibular right canine, retained deciduous canine except for left mandibular canine. Palatal bulge was identified in the maxillary left and right palatal region suggestive of the position of the impacted canines. Spacing was present between lateral incisor and canine on left side. Anterior cross-bite and rotation was present with respect to the right lateral incisor with normal overjet and overbite . Orthodontic records were taken, which included maxillary and mandibular impressions, extraoral and intraoral photographs, lateral cephalogram, orthopantomogram, and cone beam computed tomography . The panoramic radiograph showed all permanent teeth including developing third molar buds and impacted maxillary right and left canine. The left and right maxillary canine were mesially inclined toward the midline with angulation to the midline of 31° and 30° respectively. They were overlapping, the mesial third of the maxillary lateral incisor and as par the sector classification 3 were in sector IV . The CBCT evaluation of impacted canines was done in relation to adjacent teeth.
3.921875
0.98291
sec[1]/p[0]
en
0.999995
29104396
https://doi.org/10.5005/jp-journals-10005-1457
[ "maxillary", "canine", "teeth", "canines", "mandibular", "impacted", "incisor", "retained", "region", "extraoral" ]
[ { "code": "DA06.Z", "title": "Diseases of jaws, unspecified" }, { "code": "CA0A.Y&XA1R64", "title": "Maxillary fistula" }, { "code": "DA0E.0Y&XA7VK5", "title": "Maxillary hypoplasia" }, { "code": "CA0J.Y&XA1R64", "title": "Maxillary sinus polyp" }, { "code": "NA0Z&XA7VK5", "title": "Injury of maxilla" }, { "code": "2B64.Z", "title": "Malignant neoplasms of floor of mouth, unspecified" }, { "code": "DA07.6Y", "title": "Other specified disturbances in tooth eruption" }, { "code": "LA30.0", "title": "Anodontia" }, { "code": "QA00.8", "title": "Dental examination" }, { "code": "LA30.3", "title": "Hyperdontia" } ]
=== ICD-11 CODES FOUND === [DA06.Z] Diseases of jaws, unspecified Also known as: Diseases of jaws, unspecified | Diseases of jaws | disease of jaw | diseases of the jaws | disorder of jaw [2B64.Z] Malignant neoplasms of floor of mouth, unspecified Also known as: Malignant neoplasms of floor of mouth, unspecified | Malignant neoplasms of floor of mouth | cancer of mouth floor | malignant neoplasm anterior to the premolar-canine junction | malignant neoplasm of floor of mouth, unspecified [DA07.6Y] Other specified disturbances in tooth eruption Also known as: Other specified disturbances in tooth eruption | Neonatal teeth | Natal teeth | Advanced tooth eruption | precocious dentition Includes: Neonatal teeth | Advanced tooth eruption [LA30.0] Anodontia Definition: Anodontia is a genetic disorder commonly defined as the absence of all teeth, affecting both temporary and permanent dentitions, and is extremely rarely encountered in a pure form without any associated abnormalities. Rare but more common than complete anodontia is hypodontia. Also known as: Anodontia | agomphiasis | agomphosis | anodontism | complete absence of teeth [QA00.8] Dental examination Also known as: Dental examination | examination of teeth [LA30.3] Hyperdontia Definition: Hyperdontia is the condition of having supernumerary teeth, or teeth which appear in addition to the regular number of teeth. Also known as: Hyperdontia | Supplementary teeth | Supernumerary teeth | supernumerary tooth | supplemental teeth Includes: Supplementary teeth | Supernumerary teeth | distomolar === GRAPH WALKS === --- Walk 1 --- [DA06.Z] Diseases of jaws, unspecified --PARENT--> [DA06] Diseases of jaws Def: A group of diseases which are associated with the jaws and which are not classified elsewhere.... --PARENT--> [?] Diseases or disorders of orofacial complex Def: Morbid process, derangement or abnormality localised in the mouth or related tissues of the face... --- Walk 2 --- [DA06.Z] Diseases of jaws, unspecified --PARENT--> [DA06] Diseases of jaws Def: A group of diseases which are associated with the jaws and which are not classified elsewhere.... --PARENT--> [?] Diseases or disorders of orofacial complex Def: Morbid process, derangement or abnormality localised in the mouth or related tissues of the face...
[ "[DA06.Z] Diseases of jaws, unspecified\n --PARENT--> [DA06] Diseases of jaws\n Def: A group of diseases which are associated with the jaws and which are not classified elsewhere....\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...", "[DA06.Z] Diseases of jaws, unspecified\n --PARENT--> [DA06] Diseases of jaws\n Def: A group of diseases which are associated with the jaws and which are not classified elsewhere....\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..." ]
DA06.Z
Diseases of jaws, unspecified
[ { "from_icd11": "2B64.Z", "icd10_code": "C048", "icd10_title": "Malignant neoplasm of overlapping sites of floor of mouth" }, { "from_icd11": "2B64.Z", "icd10_code": "C040", "icd10_title": "Malignant neoplasm of anterior floor of mouth" }, { "from_icd11": "2B64.Z", "icd10_code": "C049", "icd10_title": "Malignant neoplasm of floor of mouth, unspecified" }, { "from_icd11": "2B64.Z", "icd10_code": "C041", "icd10_title": "Malignant neoplasm of lateral floor of mouth" }, { "from_icd11": "2B64.Z", "icd10_code": "C04", "icd10_title": "Malignant neoplasm of floor of mouth" }, { "from_icd11": "LA30.0", "icd10_code": "K000", "icd10_title": "Anodontia" }, { "from_icd11": "QA00.8", "icd10_code": "Z012", "icd10_title": "Encounter for dental examination and cleaning" }, { "from_icd11": "LA30.3", "icd10_code": "K001", "icd10_title": "Supernumerary teeth" } ]
C048
Malignant neoplasm of overlapping sites of floor of mouth
A 52-year-old female with a BMI of 21.7 kg/m 2 and ASA II classification had a thoracic epidural placed at the thoracic 10-11 level immediately after her explorative laparotomy with a total abdominal hysterectomy and bilateral salpingo-oophorectomy surgery for pain control. She had a past medical history of uterine cancer, idiopathic thrombocytopenic purpura, and anxiety. She was allergic to penicillin. She was on a patient-controlled epidural analgesia with 0.06% bupivacaine, oral acetaminophen, and intravenous hydromorphone for pain control. On examination, her vital signs and laboratory values were within normal limits. On the first and second days after surgery, she had inadequate pain control, and during the examination, reported an inconsistent loss of sensations only over the left thoracoabdominal region, which did not improve despite all the readjustment maneuvers. Hence, an ultrasound evaluation of the catheter was done with the patient in a sitting position and along the parasagittal oblique view, which revealed that the catheter tip was not in the epidural space . It was subsequently replaced at the thoracic eight-nine level with satisfactory blockade and pain control. It was used for the next couple of days with the previous regimen until the patient was able to transition to oral acetaminophen and oxycodone. She was later discharged home the day after the catheter was discontinued.
3.748047
0.98291
sec[1]/p[7]
en
0.999996
39564044
https://doi.org/10.7759/cureus.71916
[ "pain", "control", "thoracic", "epidural", "catheter", "oral", "acetaminophen", "which", "classification", "immediately" ]
[ { "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": "6C01.Z", "title": "Encopresis, unspecified" }, { "code": "6C00.Z", "title": "Enuresis, unspecified" }, { "code": "MF50.2Z", "title": "Urinary incontinence, unspecified" }, { "code": "5A14", "title": "Diabetes mellitus, type unspecified" }, { "code": "6C0Z", "title": "Elimination disorders, unspecified" } ]
=== ICD-11 CODES FOUND === [MG3Z] Pain, unspecified Also known as: Pain, unspecified | pain observations | pain NOS | generalised pain | generalised pain, NOS [8E43.Z] Pain disorders, unspecified Also known as: Pain disorders, unspecified | Pain disorders [MG31.Z] Acute pain, unspecified Also known as: Acute pain, unspecified | Acute pain [MG30.Z] Chronic pain, unspecified Also known as: Chronic pain, unspecified | Chronic pain [FB56.2] Myalgia Definition: This is a disorder characterised by pain in a muscle or group of muscles. Also known as: Myalgia | muscle ache | muscle soreness | muscular pain | myalgic Excludes: Chronic primary musculoskeletal pain | Chronic secondary musculoskeletal pain [6C01.Z] Encopresis, unspecified Also known as: Encopresis, unspecified | Encopresis | Problems of bowel control | encopresis of nonorganic origin | faecal incontinence of nonorganic origin [6C00.Z] Enuresis, unspecified Also known as: Enuresis, unspecified | Enuresis | Functional enuresis | Problems of bladder control | enuresis NOS [MF50.2Z] Urinary incontinence, unspecified Also known as: Urinary incontinence, unspecified | Urinary incontinence | urinary incontinence, NOS | bladder incontinence NOS | absence of bladder continence [5A14] Diabetes mellitus, type unspecified Also known as: Diabetes mellitus, type unspecified | diabetes NOS | DM - [diabetes mellitus] NOS | severe diabetes mellitus | sudden-onset diabetes mellitus Excludes: Idiopathic Type 1 diabetes mellitus | Type 2 diabetes mellitus | Diabetes mellitus, other specified type [6C0Z] Elimination disorders, unspecified Also known as: Elimination disorders, unspecified | Problems of bowel or bladder control === 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 --CHILD--> [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.... --- Walk 3 --- [8E43.Z] Pain disorders, unspecified --PARENT--> [8E43] Pain disorders --CHILD--> [8E43.0] Neuropathic pain Def: Neuropathic pain is described as electric, burning, or shock like, caused by metabolic, nutritional, infectious, genetic, autoimmune, and/or vasculitic processes. The pain may occur spontaneously, wit... --- Walk 4 --- [8E43.Z] Pain disorders, unspecified --PARENT--> [8E43] Pain disorders --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--> [MG31.2] Acute postoperative pain, not elsewhere classified Def: Pain at the intervention site or caused by an intervention.... --- Walk 6 --- [MG31.Z] Acute pain, unspecified --PARENT--> [MG31] Acute pain Def: Pain with a duration of less than 3 months. This code should be used only when there is no further specification of site.... --CHILD--> [MG31.2] Acute postoperative pain, not elsewhere classified Def: Pain at the intervention site or caused by an intervention....
[ "[MG3Z] Pain, unspecified\n --PARENT--> [?] Pain\n --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 --CHILD--> [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....", "[8E43.Z] Pain disorders, unspecified\n --PARENT--> [8E43] Pain disorders\n --CHILD--> [8E43.0] Neuropathic pain\n Def: Neuropathic pain is described as electric, burning, or shock like, caused by metabolic, nutritional, infectious, genetic, autoimmune, and/or vasculitic processes. The pain may occur spontaneously, wit...", "[8E43.Z] Pain disorders, unspecified\n --PARENT--> [8E43] Pain disorders\n --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--> [MG31.2] Acute postoperative pain, not elsewhere classified\n Def: Pain at the intervention site or caused by an intervention....", "[MG31.Z] Acute pain, unspecified\n --PARENT--> [MG31] Acute pain\n Def: Pain with a duration of less than 3 months.\n\nThis code should be used only when there is no further specification of site....\n --CHILD--> [MG31.2] Acute postoperative pain, not elsewhere classified\n Def: Pain at the intervention site or caused by an intervention...." ]
MG3Z
Pain, unspecified
[ { "from_icd11": "MG3Z", "icd10_code": "R52", "icd10_title": "Pain, unspecified" }, { "from_icd11": "MG3Z", "icd10_code": "R529", "icd10_title": "" }, { "from_icd11": "MG31.Z", "icd10_code": "R520", "icd10_title": "" }, { "from_icd11": "MG30.Z", "icd10_code": "R521", "icd10_title": "" }, { "from_icd11": "MG30.Z", "icd10_code": "R522", "icd10_title": "" }, { "from_icd11": "FB56.2", "icd10_code": "M7918", "icd10_title": "Myalgia, other site" }, { "from_icd11": "FB56.2", "icd10_code": "M7910", "icd10_title": "Myalgia, unspecified site" }, { "from_icd11": "FB56.2", "icd10_code": "M7912", "icd10_title": "Myalgia of auxiliary muscles, head and neck" }, { "from_icd11": "FB56.2", "icd10_code": "M791", "icd10_title": "Myalgia" }, { "from_icd11": "6C01.Z", "icd10_code": "F981", "icd10_title": "Encopresis not due to a substance or known physiological condition" }, { "from_icd11": "6C00.Z", "icd10_code": "F980", "icd10_title": "Enuresis not due to a substance or known physiological condition" }, { "from_icd11": "MF50.2Z", "icd10_code": "N39498", "icd10_title": "Other specified urinary incontinence" }, { "from_icd11": "MF50.2Z", "icd10_code": "N3941", "icd10_title": "Urge incontinence" }, { "from_icd11": "MF50.2Z", "icd10_code": "N3946", "icd10_title": "Mixed incontinence" }, { "from_icd11": "MF50.2Z", "icd10_code": "N3945", "icd10_title": "Continuous leakage" } ]
R52
Pain, unspecified
• Ventilator-associated pneumonia (VAP): Carbapenem-resistant Acinetobacter baumannii (CRAB) ( Table 2 ) was isolated from the Bronchoalveolar lavage (BAL) fluid. Meropenem was discontinued, and sulbactam was added to the Polymyxin B regimen. Subsequently, the patient underwent a tracheostomy on day 7. Fig. 1 a showing bilateral infiltrates during the initiation of treatment. With aggressive respiratory care and prone positioning, the patient gradually improved over the following days. Table 2 Antibiotic susceptibility of the Acinetobacter baumannii complex isolate recovered from this patient. Table 2 Antibiotics Interpretation MIC (mu/ml) Tigecycline Sensitive NA Ceftriaxone/Sulbactam/EDTA Sensitive NA Colistin Intermediate 1 Piperacillin/Tazobactam Resistant ≥ 128 Ceftazidime Resistant ≥ 64 Cefoperazone/Sulbactam Resistant ≥ 64 Cefepime Resistant ≥ 32 Aztreonam Resistant ≥ 64 Imipenem Resistant ≥ 16 Meropenem Resistant ≥ 16 Amikacin Resistant ≥ 64 Gentamicin Resistant ≥ 16 Ciprofloxacin Resistant ≥ 4 Levofloxacin Resistant ≥ 8 Minocycline Resistant 16 Trimethoprim/Sulfamethoxazole Resistant ≥ 320 Ampicillin/Sulbactam Resistant NA Method: Conventional Aerobic Culture. Semiquantitative/standard Loop. Susceptibility by Disc Diffusion/Automated MIC. Fig. 1 a) Chest X ray showing bilateral infiltrates (day 7 after admission); b) Resolution of pneumonia after treatment (day 21 of admission). Fig. 1
3.947266
0.93457
sec[3]/sec[4]/p[0]
en
0.999994
40115001
https://doi.org/10.1016/j.toxrep.2025.101968
[ "resistant", "sulbactam", "pneumonia", "acinetobacter", "baumannii", "meropenem", "infiltrates", "susceptibility", "sensitive", "ventilator" ]
[ { "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": "CA40.Z", "title": "Pneumonia, organism unspecified" }, { "code": "CA40.Y", "title": "Other specified pneumonia" }, { "code": "KB24", "title": "Congenital pneumonia" }, { "code": "CA40.1Z", "title": "Viral pneumonia, unspecified" }, { "code": "CA40.0Z", "title": "Bacterial pneumonia, unspecified" } ]
=== 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 [CA40.Z] Pneumonia, organism unspecified Also known as: Pneumonia, organism unspecified | Pneumonia | infectious pneumonia | PN - [pneumonia] | lobar pneumonia NOS [CA40.Y] Other specified pneumonia Also known as: Other specified pneumonia | Pneumonia in parasitic diseases | Late acquired pneumonia | Late-onset pneumonia due to other organisms | Pleuropneumonia [KB24] Congenital pneumonia Definition: Congenital pneumonia is an acute respiratory infection contracted prenatally or during the intrapartum period that is caused by a virus, bacteria, or fungi. Also known as: Congenital pneumonia | acute congenital pneumonia | congenital double pneumonia | congenital purulent pneumonia | congenital infective pneumonia Includes: infective pneumonia acquired in utero or during birth Excludes: Neonatal aspiration syndromes | Pneumonitis [CA40.1Z] Viral pneumonia, unspecified Also known as: Viral pneumonia, unspecified | Viral pneumonia | acute viral pneumonia | bronchopneumonia due to viruses other than influenza viruses | interstitial viral pneumonia [CA40.0Z] Bacterial pneumonia, unspecified Also known as: Bacterial pneumonia, unspecified | Bacterial pneumonia | acute bacillus pneumonia | acute bacterial pneumonia | bacillus double pneumonia === GRAPH WALKS === --- Walk 1 --- [MG55.0] Artemisinin resistant Plasmodium falciparum --PARENT--> [MG55] Finding of parasite resistant to antimicrobial drugs --CHILD--> [MG55.Z] Finding of parasite resistant to antimicrobial drugs, unspecified --- Walk 2 --- [MG55.0] Artemisinin resistant Plasmodium falciparum --PARENT--> [MG55] Finding of parasite resistant to antimicrobial drugs --CHILD--> [MG55.Y] Other specified finding of parasite resistant to antimicrobial drugs --- 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... --CHILD--> [5A74.0] Acquired adrenocortical insufficiency Def: This is a acquired condition in which the adrenal glands do not produce adequate amounts of steroid hormones, primarily cortisol; but may also include impaired production of aldosterone (a mineralocor... --- 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... --CHILD--> [5A74.0] Acquired adrenocortical insufficiency Def: This is a acquired condition in which the adrenal glands do not produce adequate amounts of steroid hormones, primarily cortisol; but may also include impaired production of aldosterone (a mineralocor... --- Walk 5 --- [5A44] Insulin-resistance syndromes --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 6 --- [5A44] Insulin-resistance syndromes --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....
[ "[MG55.0] Artemisinin resistant Plasmodium falciparum\n --PARENT--> [MG55] Finding of parasite resistant to antimicrobial drugs\n --CHILD--> [MG55.Z] Finding of parasite resistant to antimicrobial drugs, unspecified", "[MG55.0] Artemisinin resistant Plasmodium falciparum\n --PARENT--> [MG55] Finding of parasite resistant to antimicrobial drugs\n --CHILD--> [MG55.Y] Other specified finding of parasite resistant to antimicrobial drugs", "[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 --CHILD--> [5A74.0] Acquired adrenocortical insufficiency\n Def: This is a acquired condition in which the adrenal glands do not produce adequate amounts of steroid hormones, primarily cortisol; but may also include impaired production of aldosterone (a mineralocor...", "[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 --CHILD--> [5A74.0] Acquired adrenocortical insufficiency\n Def: This is a acquired condition in which the adrenal glands do not produce adequate amounts of steroid hormones, primarily cortisol; but may also include impaired production of aldosterone (a mineralocor...", "[5A44] Insulin-resistance syndromes\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....", "[5A44] Insulin-resistance syndromes\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...." ]
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": "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": "" } ]
E10-E14
On the morning of postoperative day one, the patient’s blood pressure was 133/65 mmHg, and magnesium sulfate was discontinued 24 hours following delivery. However, labetalol 200 mg two times a day was continued as blood pressures ranged from 114-155/55-86 bpm throughout the day. At this point, she had received a total amount of 3,340 mL intravenous fluids, which were also discontinued at this time. Her intake and output of fluids are shown in Table 4 . The patient reported dyspnea with nasal congestion and coughing that improved with sitting up. Inspiratory stridor was heard, but the lungs were clear to auscultation. She had 1+ pitting edema of the lower extremities. On 4 L/min of supplemental oxygen via nasal cannula, oxygen saturations were 89-90%. By the late afternoon, her dyspnea was worsening, and she was requiring up to 10 L/min of supplemental oxygen. At this time, wet lung sounds were heard on auscultation. Labs showed increased leukocytosis but she remained afebrile (Table 2 ). Testing for COVID-19, influenza, and respiratory syncytial virus were negative. A computed tomography angiography (CTA), as shown in Figure 1 , was ordered and showed pulmonary edema with possible pneumonia and pulmonary hypertension. Intravenous furosemide was started, and her urine output was monitored. Other interventions to improve breathing included pulmonary hygiene and the use of an incentive spirometer.
3.697266
0.980469
sec[1]/p[3]
en
0.999996
39224732
https://doi.org/10.7759/cureus.66065
[ "this", "oxygen", "pulmonary", "blood", "discontinued", "intravenous", "fluids", "time", "output", "shown" ]
[ { "code": "4A01.03", "title": "Transient hypogammaglobulinaemia of infancy" }, { "code": "MD11.1", "title": "Asphyxia" }, { "code": "NE60", "title": "Harmful effects of drugs, medicaments or biological substances, not elsewhere classified" }, { "code": "3A51.7", "title": "High affinity haemoglobin" }, { "code": "NF05", "title": "Asphyxiation" }, { "code": "PB08", "title": "Unintentional threat to breathing from low oxygen environment" }, { "code": "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 === [4A01.03] Transient hypogammaglobulinaemia of infancy Also known as: Transient hypogammaglobulinaemia of infancy | immunoglobulin maturational delay | THI - [transient hypogammaglobulinaemia of infancy] [MD11.1] Asphyxia Definition: Asphyxia is a life-threatening condition in which oxygen is prevented from reaching the tissues by obstruction of or damage to any part of the respiratory system. More generally the term indicates all the conditions generating impaired or impeded breathing. Also known as: Asphyxia | pathological asphyxia | decreased oxygen supply | oxygen deficiency | positional asphyxia Excludes: asphyxia due to foreign body in respiratory tract | asphyxia due to carbon monoxide | asphyxia due to traumatic [NE60] Harmful effects of drugs, medicaments or biological substances, not elsewhere classified Also known as: Harmful effects of drugs, medicaments or biological substances, not elsewhere classified | drugs, medicaments or biological substances, toxicity not elsewhere classified | adverse drug effects | drug reaction NOS | drug allergy NOS Excludes: Alcohol intoxication | pathological drug intoxication | hypersensitivity reaction to correctly administered drug [3A51.7] High affinity haemoglobin Definition: A disease caused by determinants arising after birth, in the antenatal period or by genetically inherited factors leading to high oxygen affinity haemoglobin. This disease is characterised by abnormalities in the globin chains that alter the affinity of the haemoglobin molecule for oxygen, affecting the normal loading of oxygen in the lungs and delivery of oxygen to the tissues. Also known as: High affinity haemoglobin | Haemoglobins with abnormal oxygen affinity [NF05] Asphyxiation Also known as: Asphyxiation | suffocation NOS | traumatic asphyxia | positional asphyxiation | asphyxia (ligature) Excludes: Respiratory distress of newborn | Adult acute respiratory distress syndrome | asphyxia from carbon monoxide [PB08] Unintentional threat to breathing from low oxygen environment Also known as: Unintentional threat to breathing from low oxygen environment | confined to or trapped in a low-oxygen environment | Accidental mechanical suffocation in refrigerator | Diving with insufficient air supply | Accidentally shut in other airtight space [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 --- [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 --- [MD11.1] Asphyxia Def: Asphyxia is a life-threatening condition in which oxygen is prevented from reaching the tissues by obstruction of or damage to any part of the respiratory system. More generally the term indicates all... --RELATED_TO--> [?] Intrauterine hypoxia Def: Intrauterine hypoxia occurs when the fetus is deprived of an adequate supply of oxygen. This may occur with prolapse or occlusion of the umbilical cord, placental infarction and maternal smoking. This... --EXCLUDES--> [?] Hypoxic ischaemic encephalopathy of newborn Def: Hypoxic ischaemic encephalopathy (HIE) is when a newborn’s brain fails to receive a sufficient amount of oxygen or blood before and during birth that may lead to brain damage or death.... --- Walk 4 --- [MD11.1] Asphyxia Def: Asphyxia is a life-threatening condition in which oxygen is prevented from reaching the tissues by obstruction of or damage to any part of the respiratory system. More generally the term indicates all... --EXCLUDES--> [?] Injury, poisoning or certain other consequences of external causes Def: !markdown In the ICD, injury means physical or physiological bodily harm resulting from interaction of the body with energy (mechanical, thermal, electrical, chemical or radiant, or due to extreme pre... --CHILD--> [?] Injuries to the neck --- Walk 5 --- [NE60] Harmful effects of drugs, medicaments or biological substances, not elsewhere classified --EXCLUDES--> [?] Disorders due to substance use or addictive behaviours Def: Disorders due to substance use and addictive behaviours are mental and behavioural disorders that develop as a result of the use of predominantly psychoactive substances, including medications, or spe... --CHILD--> [?] Disorders due to addictive behaviours Def: Disorders due to addictive behaviours are recognizable and clinically significant syndromes associated with distress or interference with personal functions that develop as a result of repetitive rewa... --- Walk 6 --- [NE60] Harmful effects of drugs, medicaments or biological substances, not elsewhere classified --EXCLUDES--> [?] Alcohol intoxication Def: Alcohol intoxication is a clinically significant transient condition that develops during or shortly after the consumption of alcohol that is characterised by disturbances in consciousness, cognition,... --EXCLUDES--> [?] Possession trance disorder Def: Possession trance disorder is characterised by trance states in which there is a marked alteration in the individual’s state of consciousness and the individual’s customary sense of personal identity ...
[ "[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", "[MD11.1] Asphyxia\n Def: Asphyxia is a life-threatening condition in which oxygen is prevented from reaching the tissues by obstruction of or damage to any part of the respiratory system. More generally the term indicates all...\n --RELATED_TO--> [?] Intrauterine hypoxia\n Def: Intrauterine hypoxia occurs when the fetus is deprived of an adequate supply of oxygen. This may occur with prolapse or occlusion of the umbilical cord, placental infarction and maternal smoking. This...\n --EXCLUDES--> [?] Hypoxic ischaemic encephalopathy of newborn\n Def: Hypoxic ischaemic encephalopathy (HIE) is when a newborn’s brain fails to receive a sufficient amount of oxygen or blood before and during birth that may lead to brain damage or death....", "[MD11.1] Asphyxia\n Def: Asphyxia is a life-threatening condition in which oxygen is prevented from reaching the tissues by obstruction of or damage to any part of the respiratory system. More generally the term indicates all...\n --EXCLUDES--> [?] Injury, poisoning or certain other consequences of external causes\n Def: !markdown\nIn the ICD, injury means physical or physiological bodily harm resulting from interaction of the body with energy (mechanical, thermal, electrical, chemical or radiant, or due to extreme pre...\n --CHILD--> [?] Injuries to the neck", "[NE60] Harmful effects of drugs, medicaments or biological substances, not elsewhere classified\n --EXCLUDES--> [?] Disorders due to substance use or addictive behaviours\n Def: Disorders due to substance use and addictive behaviours are mental and behavioural disorders that develop as a result of the use of predominantly psychoactive substances, including medications, or spe...\n --CHILD--> [?] Disorders due to addictive behaviours\n Def: Disorders due to addictive behaviours are recognizable and clinically significant syndromes associated with distress or interference with personal functions that develop as a result of repetitive rewa...", "[NE60] Harmful effects of drugs, medicaments or biological substances, not elsewhere classified\n --EXCLUDES--> [?] Alcohol intoxication\n Def: Alcohol intoxication is a clinically significant transient condition that develops during or shortly after the consumption of alcohol that is characterised by disturbances in consciousness, cognition,...\n --EXCLUDES--> [?] Possession trance disorder\n Def: Possession trance disorder is characterised by trance states in which there is a marked alteration in the individual’s state of consciousness and the individual’s customary sense of personal identity ..." ]
4A01.03
Transient hypogammaglobulinaemia of infancy
[ { "from_icd11": "4A01.03", "icd10_code": "D807", "icd10_title": "Transient hypogammaglobulinemia of infancy" }, { "from_icd11": "MD11.1", "icd10_code": "R0901", "icd10_title": "Asphyxia" }, { "from_icd11": "MD11.1", "icd10_code": "R0902", "icd10_title": "Hypoxemia" }, { "from_icd11": "MD11.1", "icd10_code": "R090", "icd10_title": "Asphyxia and hypoxemia" }, { "from_icd11": "NE60", "icd10_code": "T50A95A", "icd10_title": "Adverse effect of other bacterial vaccines, initial encounter" }, { "from_icd11": "NE60", "icd10_code": "T50Z15A", "icd10_title": "Adverse effect of immunoglobulin, initial encounter" }, { "from_icd11": "NE60", "icd10_code": "T50Z95A", "icd10_title": "Adverse effect of other vaccines and biological substances, initial encounter" }, { "from_icd11": "NE60", "icd10_code": "T50A95S", "icd10_title": "Adverse effect of other bacterial vaccines, sequela" }, { "from_icd11": "NE60", "icd10_code": "T50B95A", "icd10_title": "Adverse effect of other viral vaccines, initial encounter" }, { "from_icd11": "NE60", "icd10_code": "T50A25A", "icd10_title": "Adverse effect of mixed bacterial vaccines without a pertussis component, initial encounter" }, { "from_icd11": "NE60", "icd10_code": "T50A91A", "icd10_title": "Poisoning by other bacterial vaccines, accidental (unintentional), initial encounter" }, { "from_icd11": "NE60", "icd10_code": "T498X5A", "icd10_title": "Adverse effect of other topical agents, initial encounter" }, { "from_icd11": "NE60", "icd10_code": "T48905A", "icd10_title": "Adverse effect of unspecified agents primarily acting on the respiratory system, initial encounter" }, { "from_icd11": "NE60", "icd10_code": "T48995A", "icd10_title": "Adverse effect of other agents primarily acting on the respiratory system, initial encounter" }, { "from_icd11": "NE60", "icd10_code": "T50A15A", "icd10_title": "Adverse effect of pertussis vaccine, including combinations with a pertussis component, initial encounter" } ]
D807
Transient hypogammaglobulinemia of infancy
The first treatment cycle (administered activity: 7.4GBq) was well-tolerated with only decreased appetite, mild nausea, and fatigue. Following the first cycle, his PSA value slightly increased to 48.23 ng/mL. Six weeks later, he presented to the emergency department (ED) with increased nausea and vomiting. During admission, his symptoms were successfully managed with supportive treatment, as laboratory results and an ultrasound showed no abnormalities. He received a second cycle (administered activity: 7.4GBq) without any symptoms. Post-therapy SPECT scan revealed no new metastases or progression in existing lesions. His PSA value was 61.63 ng/mL after the second cycle. Three weeks later, the patient returned to the ED with symptoms of vomiting and back pain. In the patient’s history, there was no record of previous pancreatitis, gallstones, alcohol intake, high blood lipid levels, or other identifiable risk factors for pancreatitis. Blood tests revealed slightly elevated bilirubin and liver enzyme levels. An outside CT scan identified a mass-like lesion adjacent to the pancreatic head, previously noted as PSMA-avid lymph nodes on pre-therapy [ 68 Ga] Ga-PSMA-11 PET/CT and contrast-enhanced CT imaging, which was causing biliary duct obstruction and ductal dilation. The obstruction was resolved with an ERCP procedure and common bile duct (CBD) stent placement, leading to symptomatic improvement.
3.916016
0.970215
sec[1]/p[2]
en
0.999998
39435291
https://doi.org/10.3389/fonc.2024.1442293
[ "cycle", "activity", "nausea", "slightly", "vomiting", "scan", "pancreatitis", "blood", "psma", "duct" ]
[ { "code": "6A80.5", "title": "Rapid cycling" }, { "code": "PA03", "title": "Unintentional land transport traffic event injuring a motor cyclist" }, { "code": "5C50.AZ", "title": "Disorders of urea cycle metabolism, unspecified" }, { "code": "PA23", "title": "Unintentional land transport event unknown whether traffic or nontraffic injuring a motor cyclist" }, { "code": "PA02", "title": "Unintentional land transport traffic event injuring a pedal cyclist" }, { "code": "QF2Z", "title": "Difficulty or need for assistance with unspecified activity" }, { "code": "6A05.Z", "title": "Attention deficit hyperactivity disorder, presentation unspecified" }, { "code": "QF23", "title": "Difficulty or need for assistance with mobility" }, { "code": "QF28", "title": "Difficulty or need for assistance with work activities" }, { "code": "CA40.Z", "title": "Pneumonia, organism unspecified" } ]
=== ICD-11 CODES FOUND === [6A80.5] Rapid cycling Definition: In the context of bipolar type I or bipolar type II disorder, there has been a high frequency of mood episodes (at least four) over the past 12 months. There may be a switch from one polarity of mood to the other, or the mood episodes may be demarcated by a period of remission. In individuals with a high frequency of mood episodes, some may have a shorter duration than those usually observed in bipolar type I or bipolar type II disorder. In particular, depressive periods may only last several da Also known as: Rapid cycling [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 [5C50.AZ] Disorders of urea cycle metabolism, unspecified Also known as: Disorders of urea cycle metabolism, unspecified | Disorders of urea cycle metabolism | disorder of urea cycle | disorders of metabolism of ornithine, citrulline, argininosuccinic acid, arginine and ammonia | ammonia metabolic disorder [PA23] Unintentional land transport event unknown whether traffic or nontraffic injuring a motor cyclist Also known as: Unintentional land transport event unknown whether traffic or nontraffic injuring a motor cyclist | unintentional off-road crash injuring a motor cyclist, unknown whether on road | motor bike crash NOS | motor cycle crash NOS | Motorcycle rider injured in collision with railway train or railway vehicle [PA02] Unintentional land transport traffic event injuring a pedal cyclist Also known as: Unintentional land transport traffic event injuring a pedal cyclist | Pedal cyclist injured in collision with pedestrian or animal | Pedal cyclist injured in collision with pedestrian or animal, person injured while boarding or alighting | Pedal cyclist injured in collision with pedestrian or animal, driver injured in traffic accident | Pedal cyclist injured in collision with pedestrian or animal, passenger injured in traffic accident [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 [6A05.Z] Attention deficit hyperactivity disorder, presentation unspecified Also known as: Attention deficit hyperactivity disorder, presentation unspecified | Attention deficit hyperactivity disorder | disturbance of activity and attention | disorder of activity and attention | ADHD - [attention deficit hyperactivity disorder] [QF23] Difficulty or need for assistance with mobility Also known as: Difficulty or need for assistance with mobility | difficulty with mobility | need for assistance due to reduced mobility | need for assistance with mobility | problem with impaired mobility Excludes: Abnormalities of gait or mobility [QF28] Difficulty or need for assistance with work activities Also known as: Difficulty or need for assistance with work activities | need for assistance with work activities | difficulty with work activities [CA40.Z] Pneumonia, organism unspecified Also known as: Pneumonia, organism unspecified | Pneumonia | infectious pneumonia | PN - [pneumonia] | lobar pneumonia NOS === GRAPH WALKS === --- Walk 1 --- [6A80.5] Rapid cycling Def: In the context of bipolar type I or bipolar type II disorder, there has been a high frequency of mood episodes (at least four) over the past 12 months. There may be a switch from one polarity of mood ... --PARENT--> [6A80] Symptomatic and course presentations for mood episodes in mood disorders Def: These categories may be applied to describe the presentation and characteristics of mood episodes in the context of single episode depressive disorder, recurrent depressive disorder, bipolar type I di... --CHILD--> [6A80.1] Panic attacks in mood episodes Def: In the context of a current mood episode (manic, depressive, mixed, or hypomanic), there have been recurrent panic attacks (i.e., at least two) during the past month that occur specifically in respons... --- Walk 2 --- [6A80.5] Rapid cycling Def: In the context of bipolar type I or bipolar type II disorder, there has been a high frequency of mood episodes (at least four) over the past 12 months. There may be a switch from one polarity of mood ... --PARENT--> [6A80] Symptomatic and course presentations for mood episodes in mood disorders Def: These categories may be applied to describe the presentation and characteristics of mood episodes in the context of single episode depressive disorder, recurrent depressive disorder, bipolar type I di... --CHILD--> [6A80.1] Panic attacks in mood episodes Def: In the context of a current mood episode (manic, depressive, mixed, or hypomanic), there have been recurrent panic attacks (i.e., at least two) during the past month that occur specifically in respons... --- Walk 3 --- [PA03] Unintentional land transport traffic event injuring a motor cyclist --EXCLUDES--> [?] Unintentional land transport traffic event injuring an occupant of a low powered passenger vehicle --CHILD--> [?] Occupant of three-wheeled motor vehicle injured in collision with two- or three-wheeled motor vehicle --- Walk 4 --- [PA03] Unintentional land transport traffic event injuring a motor cyclist --EXCLUDES--> [?] Unintentional land transport traffic event injuring an occupant of a low powered passenger vehicle --CHILD--> [?] Occupant of three-wheeled motor vehicle injured in collision with two- or three-wheeled motor vehicle --- Walk 5 --- [5C50.AZ] Disorders of urea cycle metabolism, unspecified --PARENT--> [5C50.A] Disorders of urea cycle metabolism --CHILD--> [5C50.A1] Carbamoylphosphate synthetase deficiency Def: Carbamyl phosphate synthetase deficiency is an urea cycle disorder strictly limited to the liver and intestine that results in congenital hyperammonemia and defective citrulline synthesis.... --- Walk 6 --- [5C50.AZ] Disorders of urea cycle metabolism, unspecified --PARENT--> [5C50.A] Disorders of urea cycle metabolism --CHILD--> [5C50.A0] Argininosuccinic aciduria Def: Argininosuccinic aciduria is an autosomal recessive inherited deficiency of argininosuccinate lyase, an enzyme involved in the urea cycle that leads to severe hyperammonemic coma in neonates or, in ch...
[ "[6A80.5] Rapid cycling\n Def: In the context of bipolar type I or bipolar type II disorder, there has been a high frequency of mood episodes (at least four) over the past 12 months. There may be a switch from one polarity of mood ...\n --PARENT--> [6A80] Symptomatic and course presentations for mood episodes in mood disorders\n Def: These categories may be applied to describe the presentation and characteristics of mood episodes in the context of single episode depressive disorder, recurrent depressive disorder, bipolar type I di...\n --CHILD--> [6A80.1] Panic attacks in mood episodes\n Def: In the context of a current mood episode (manic, depressive, mixed, or hypomanic), there have been recurrent panic attacks (i.e., at least two) during the past month that occur specifically in respons...", "[6A80.5] Rapid cycling\n Def: In the context of bipolar type I or bipolar type II disorder, there has been a high frequency of mood episodes (at least four) over the past 12 months. There may be a switch from one polarity of mood ...\n --PARENT--> [6A80] Symptomatic and course presentations for mood episodes in mood disorders\n Def: These categories may be applied to describe the presentation and characteristics of mood episodes in the context of single episode depressive disorder, recurrent depressive disorder, bipolar type I di...\n --CHILD--> [6A80.1] Panic attacks in mood episodes\n Def: In the context of a current mood episode (manic, depressive, mixed, or hypomanic), there have been recurrent panic attacks (i.e., at least two) during the past month that occur specifically in respons...", "[PA03] Unintentional land transport traffic event injuring a motor cyclist\n --EXCLUDES--> [?] Unintentional land transport traffic event injuring an occupant of a low powered passenger vehicle\n --CHILD--> [?] Occupant of three-wheeled motor vehicle injured in collision with two- or three-wheeled motor vehicle", "[PA03] Unintentional land transport traffic event injuring a motor cyclist\n --EXCLUDES--> [?] Unintentional land transport traffic event injuring an occupant of a low powered passenger vehicle\n --CHILD--> [?] Occupant of three-wheeled motor vehicle injured in collision with two- or three-wheeled motor vehicle", "[5C50.AZ] Disorders of urea cycle metabolism, unspecified\n --PARENT--> [5C50.A] Disorders of urea cycle metabolism\n --CHILD--> [5C50.A1] Carbamoylphosphate synthetase deficiency\n Def: Carbamyl phosphate synthetase deficiency is an urea cycle disorder strictly limited to the liver and intestine that results in congenital hyperammonemia and defective citrulline synthesis....", "[5C50.AZ] Disorders of urea cycle metabolism, unspecified\n --PARENT--> [5C50.A] Disorders of urea cycle metabolism\n --CHILD--> [5C50.A0] Argininosuccinic aciduria\n Def: Argininosuccinic aciduria is an autosomal recessive inherited deficiency of argininosuccinate lyase, an enzyme involved in the urea cycle that leads to severe hyperammonemic coma in neonates or, in ch..." ]
6A80.5
Rapid cycling
[ { "from_icd11": "PA03", "icd10_code": "V299XXD", "icd10_title": "Motorcycle rider (driver) (passenger) injured in unspecified traffic accident, subsequent encounter" }, { "from_icd11": "PA03", "icd10_code": "V234XXA", "icd10_title": "Motorcycle driver injured in collision with car, pick-up truck or van in traffic accident, initial encounter" }, { "from_icd11": "PA03", "icd10_code": "V299XXA", "icd10_title": "Motorcycle rider (driver) (passenger) injured in unspecified traffic accident, initial encounter" }, { "from_icd11": "PA03", "icd10_code": "V2940XA", "icd10_title": "Motorcycle driver injured in collision with unspecified motor vehicles in traffic accident, initial encounter" }, { "from_icd11": "PA03", "icd10_code": "V239XXD", "icd10_title": "Unspecified motorcycle rider injured in collision with car, pick-up truck or van in traffic accident, subsequent encounter" }, { "from_icd11": "PA03", "icd10_code": "V299XXS", "icd10_title": "Motorcycle rider (driver) (passenger) injured in unspecified traffic accident, sequela" }, { "from_icd11": "PA03", "icd10_code": "V2988XA", "icd10_title": "Motorcycle rider (driver) (passenger) injured in other specified transport accidents, initial encounter" }, { "from_icd11": "PA03", "icd10_code": "V2950XA", "icd10_title": "Motorcycle passenger injured in collision with unspecified motor vehicles in traffic accident, initial encounter" }, { "from_icd11": "PA03", "icd10_code": "V2960XA", "icd10_title": "Unspecified motorcycle rider injured in collision with unspecified motor vehicles in traffic accident, initial encounter" }, { "from_icd11": "PA03", "icd10_code": "V2949XS", "icd10_title": "Motorcycle driver injured in collision with other motor vehicles in traffic accident, sequela" }, { "from_icd11": "PA03", "icd10_code": "V234XXS", "icd10_title": "Motorcycle driver injured in collision with car, pick-up truck or van in traffic accident, sequela" }, { "from_icd11": "PA03", "icd10_code": "V235XXA", "icd10_title": "Motorcycle passenger injured in collision with car, pick-up truck or van in traffic accident, initial encounter" }, { "from_icd11": "PA03", "icd10_code": "V234XXD", "icd10_title": "Motorcycle driver injured in collision with car, pick-up truck or van in traffic accident, subsequent encounter" }, { "from_icd11": "PA03", "icd10_code": "V2949XA", "icd10_title": "Motorcycle driver injured in collision with other motor vehicles in traffic accident, initial encounter" }, { "from_icd11": "PA03", "icd10_code": "V2949XD", "icd10_title": "Motorcycle driver injured in collision with other motor vehicles in traffic accident, subsequent encounter" } ]
V299XXD
Motorcycle rider (driver) (passenger) injured in unspecified traffic accident, subsequent encounter
The patient underwent endoscope-assisted evacuation of ASDH under general anesthesia. We selected the site for craniotomy at the thickest part of the hematoma using neuronavigation. Then, a straight skin incision of 5 cm was made, and a 4-cm-diameter small parietal craniotomy was performed. The hematoma was jelly-like and had partially formed a capsule. The hematoma was aspirated with a suction tube while being observed with a 2.7-mm 0° and 30° rigid endoscope . The rigid endoscope was held in the left hand, the suction cannula was held in the right hand, and the suction cannula was exchanged for bipolar forceps, as needed. The hematoma was removed using a suction cannula under the guidance of a rigid endoscope. When bleeding from a vessel on the brain surface was observed, a suction cannula was placed at the bleeding point, and coagulation was performed using monopolar electrocoagulation with a suction cannula. The bridging vein, which we identified as the source of bleeding, was coagulated using bipolar forceps. It was covered with absorbable Fibrillar™ hemostat (Surgicel®; Ethicon, Tokyo, Japan) for bleeding points. Finally, the subdural space was irrigated with artificial cerebrospinal fluid(Artcereb, Otsuka Pharmaceutical Factory, Inc., Tokushima, Japan). The dura mater was tightly closed and the bone was repositioned and stabilized using a fixture device, followed by closure of the scalp.
3.914063
0.95752
sec[1]/p[2]
en
0.999996
39099992
https://doi.org/10.7759/cureus.63817
[ "suction", "using", "cannula", "endoscope", "hematoma", "bleeding", "rigid", "craniotomy", "held", "hand" ]
[ { "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": "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 === [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 [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 --- [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... --EXCLUDES--> [?] Disorders due to substance use Def: Disorders due to substance use include disorders that result from a single occasion or repeated use of substances that have psychoactive properties, including certain medications. Disorders related to... --- Walk 2 --- [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... --PARENT--> [?] Hazardous substance use Def: Hazardous substance use is a pattern of psychoactive substance use that appreciably increases the risk of harmful physical or mental health consequences to the user or to others to an extent that warr... --- 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... --PARENT--> [?] Disorders due to substance use or addictive behaviours Def: Disorders due to substance use and addictive behaviours are mental and behavioural disorders that develop as a result of the use of predominantly psychoactive substances, including medications, or spe... --- 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... --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 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... --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... --CHILD--> [?] Cocaine dependence Def: Cocaine dependence is a disorder of regulation of cocaine use arising from repeated or continuous use of cocaine. The characteristic feature is a strong internal drive to use cocaine, which is manifes... --- 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... --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... --EXCLUDES--> [?] 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...
[ "[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 --EXCLUDES--> [?] 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...", "[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 --PARENT--> [?] Hazardous substance use\n Def: Hazardous substance use is a pattern of psychoactive substance use that appreciably increases the risk of harmful physical or mental health consequences to the user or to others to an extent that warr...", "[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 --PARENT--> [?] Disorders due to substance use or addictive behaviours\n Def: Disorders due to substance use and addictive behaviours are mental and behavioural disorders that develop as a result of the use of predominantly psychoactive substances, including medications, or spe...", "[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...", "[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 --CHILD--> [?] Cocaine dependence\n Def: Cocaine dependence is a disorder of regulation of cocaine use arising from repeated or continuous use of cocaine. The characteristic feature is a strong internal drive to use cocaine, which is manifes...", "[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 --EXCLUDES--> [?] 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..." ]
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
The absence of insulinopenia and episodes of ketosis did not allow classification as idiopathic type 1 diabetes . Type 2 diabetes was unlikely due to age diagnosis, lack of weight, and family history of diabetes. Three monogenic diabetes that are associated with liver disease could be mentioned. The first is lipoatrophic diabetes which can lead to end-stage liver disease secondary to nonalcoholic steatohepatitis . However, our patient did not have a paucity of fat or insulin resistance to suggest lipoatrophic diabetes. The association between Maturity-onset diabetes of the young type 3 (MODY-3) and liver adenomatosis has been reported . However, liver adenomatosis does not lead directly to end-stage liver disease. The association between MODY-5 and an increased liver enzyme has been reported . Candidates for genetic testing for MODY include nonobese subjects with hyperglycemia, no evidence of Î 2 -cell autoimmunity, preserved Î 2 -cell function, and a strong family history of similar-type diabetes among first-degree relatives . Although this patient had many criteria in favor of, the probability of MODY seemed low in the absence of a family history of similar diabetes in first-degree relatives and high insulin requirements. Because his clinical profile did not fit with one of the known MODY types, genetic testing was not performed given the cost and logistic constraints associated with testing.
4.132813
0.63916
sec[2]/p[1]
en
0.999996
PMC12032616
https://doi.org/10.11604/pamj.2025.50.16.46217
[ "diabetes", "liver", "mody", "type", "family", "testing", "absence", "associated", "lipoatrophic", "lead" ]
[ { "code": "5A14", "title": "Diabetes mellitus, type unspecified" }, { "code": "JA63.2", "title": "Diabetes mellitus arising in pregnancy" }, { "code": "5A13.4", "title": "Diabetes mellitus due to drug or chemical" }, { "code": "LD2H.Y", "title": "Other specified syndromic genetic deafness" }, { "code": "5C64.3", "title": "Disorders of phosphorus metabolism or phosphatases" }, { "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 === [5A14] Diabetes mellitus, type unspecified Also known as: Diabetes mellitus, type unspecified | diabetes NOS | DM - [diabetes mellitus] NOS | severe diabetes mellitus | sudden-onset diabetes mellitus Excludes: Idiopathic Type 1 diabetes mellitus | Type 2 diabetes mellitus | Diabetes mellitus, other specified type [JA63.2] Diabetes mellitus arising in pregnancy Definition: Diabetes mellitus arising or diagnosed in pregnancy (Gestational diabetes mellitus) per WHO criteria or other national criteria. Gestational diabetes mellitus is defined as any degree of glucose intolerance with onset or first recognition during pregnancy. The definition applies regardless of whether insulin or only diet modification is used for treatment or whether the condition persists after pregnancy. Also known as: Diabetes mellitus arising in pregnancy | diabetes of pregnancy | GDM - [gestational diabetes mellitus] | gestational diabetes | maternal gestational diabetes mellitus [5A13.4] Diabetes mellitus due to drug or chemical Definition: Other specified diabetes mellitus due to drug or chemical is a form of diabetes, which is caused by drug or chemical substance that impairs insulin secretion and insulin action. Also known as: Diabetes mellitus due to drug or chemical | chemical diabetes | chemical DM | Steroid-induced diabetes [LD2H.Y] Other specified syndromic genetic deafness Also known as: Other specified syndromic genetic deafness | Albinism - black lock - cell migration disorder of the neurocytes of the gut - sensorineural deafness | ABCD - [Albinism - black lock - cell migration disorder of the neurocytes of the gut - sensorineural deafness] syndrome | Albinism-deafness syndrome | Alström syndrome [5C64.3] Disorders of phosphorus metabolism or phosphatases Definition: Any condition caused by errors in phosphorus metabolism, or in phosphatase activity. Also known as: Disorders of phosphorus metabolism or phosphatases | disorders of phosphorus metabolism | Hypophosphatasia | Rathbun syndrome | Congenital hypophosphatasia Includes: Hypophosphatasia Excludes: Adult osteomalacia | Osteoporosis [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 --- [5A14] Diabetes mellitus, type unspecified --EXCLUDES--> [?] Type 2 diabetes mellitus Def: Diabetes mellitus type 2 (formerly noninsulin-dependent diabetes mellitus (NIDDM) or adult-onset diabetes) is a metabolic disorder that is characterised by high blood glucose in the context of insulin... --EXCLUDES--> [?] Diabetes mellitus, other specified type Def: Diabetes mellitus which cannot be classified as either Type 1 or Type 2 diabetes mellitus.... --- Walk 2 --- [5A14] Diabetes mellitus, type unspecified --EXCLUDES--> [?] Idiopathic Type 1 diabetes mellitus Def: Some forms of type 1 diabetes mellitus have no known aetiologies. These patients have permanent insulinopenia and are prone to ketoacidosis, but have no evidence of β-cell autoimmunity. Although only ... --PARENT--> [?] Type 1 diabetes mellitus Def: Diabetes mellitus type 1 (type 1 diabetes, T1DM, formerly insulin dependent or juvenile diabetes) is a form of diabetes mellitus that results from destruction of insulin-producing beta cells, mostly b... --- Walk 3 --- [JA63.2] Diabetes mellitus arising in pregnancy Def: Diabetes mellitus arising or diagnosed in pregnancy (Gestational diabetes mellitus) per WHO criteria or other national criteria. Gestational diabetes mellitus is defined as any degree of glucose intol... --PARENT--> [JA63] 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... --CHILD--> [JA63.1] Pre-existing type 2 diabetes mellitus in pregnancy --- Walk 4 --- [JA63.2] Diabetes mellitus arising in pregnancy Def: Diabetes mellitus arising or diagnosed in pregnancy (Gestational diabetes mellitus) per WHO criteria or other national criteria. Gestational diabetes mellitus is defined as any degree of glucose intol... --PARENT--> [JA63] 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... --CHILD--> [JA63.0] Pre-existing type 1 diabetes mellitus in pregnancy --- Walk 5 --- [5A13.4] Diabetes mellitus due to drug or chemical Def: Other specified diabetes mellitus due to drug or chemical is a form of diabetes, which is caused by drug or chemical substance that impairs insulin secretion and insulin action.... --PARENT--> [5A13] Diabetes mellitus, other specified type Def: Diabetes mellitus which cannot be classified as either Type 1 or Type 2 diabetes mellitus.... --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... --- Walk 6 --- [5A13.4] Diabetes mellitus due to drug or chemical Def: Other specified diabetes mellitus due to drug or chemical is a form of diabetes, which is caused by drug or chemical substance that impairs insulin secretion and insulin action.... --PARENT--> [5A13] Diabetes mellitus, other specified type Def: Diabetes mellitus which cannot be classified as either Type 1 or Type 2 diabetes mellitus.... --EXCLUDES--> [?] Type 2 diabetes mellitus Def: Diabetes mellitus type 2 (formerly noninsulin-dependent diabetes mellitus (NIDDM) or adult-onset diabetes) is a metabolic disorder that is characterised by high blood glucose in the context of insulin...
[ "[5A14] Diabetes mellitus, type unspecified\n --EXCLUDES--> [?] Type 2 diabetes mellitus\n Def: Diabetes mellitus type 2 (formerly noninsulin-dependent diabetes mellitus (NIDDM) or adult-onset diabetes) is a metabolic disorder that is characterised by high blood glucose in the context of insulin...\n --EXCLUDES--> [?] Diabetes mellitus, other specified type\n Def: Diabetes mellitus which cannot be classified as either Type 1 or Type 2 diabetes mellitus....", "[5A14] Diabetes mellitus, type unspecified\n --EXCLUDES--> [?] Idiopathic Type 1 diabetes mellitus\n Def: Some forms of type 1 diabetes mellitus have no known aetiologies. These patients have permanent insulinopenia and are prone to ketoacidosis, but have no evidence of β-cell autoimmunity. Although only ...\n --PARENT--> [?] Type 1 diabetes mellitus\n Def: Diabetes mellitus type 1 (type 1 diabetes, T1DM, formerly insulin dependent or juvenile diabetes) is a form of diabetes mellitus that results from destruction of insulin-producing beta cells, mostly b...", "[JA63.2] Diabetes mellitus arising in pregnancy\n Def: Diabetes mellitus arising or diagnosed in pregnancy (Gestational diabetes mellitus) per WHO criteria or other national criteria. Gestational diabetes mellitus is defined as any degree of glucose intol...\n --PARENT--> [JA63] 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...\n --CHILD--> [JA63.1] Pre-existing type 2 diabetes mellitus in pregnancy", "[JA63.2] Diabetes mellitus arising in pregnancy\n Def: Diabetes mellitus arising or diagnosed in pregnancy (Gestational diabetes mellitus) per WHO criteria or other national criteria. Gestational diabetes mellitus is defined as any degree of glucose intol...\n --PARENT--> [JA63] 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...\n --CHILD--> [JA63.0] Pre-existing type 1 diabetes mellitus in pregnancy", "[5A13.4] Diabetes mellitus due to drug or chemical\n Def: Other specified diabetes mellitus due to drug or chemical is a form of diabetes, which is caused by drug or chemical substance that impairs insulin secretion and insulin action....\n --PARENT--> [5A13] Diabetes mellitus, other specified type\n Def: Diabetes mellitus which cannot be classified as either Type 1 or Type 2 diabetes mellitus....\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...", "[5A13.4] Diabetes mellitus due to drug or chemical\n Def: Other specified diabetes mellitus due to drug or chemical is a form of diabetes, which is caused by drug or chemical substance that impairs insulin secretion and insulin action....\n --PARENT--> [5A13] Diabetes mellitus, other specified type\n Def: Diabetes mellitus which cannot be classified as either Type 1 or Type 2 diabetes mellitus....\n --EXCLUDES--> [?] Type 2 diabetes mellitus\n Def: Diabetes mellitus type 2 (formerly noninsulin-dependent diabetes mellitus (NIDDM) or adult-onset diabetes) is a metabolic disorder that is characterised by high blood glucose in the context of insulin..." ]
5A14
Diabetes mellitus, type unspecified
[ { "from_icd11": "5A14", "icd10_code": "E14", "icd10_title": "" }, { "from_icd11": "5A14", "icd10_code": "E140", "icd10_title": "" }, { "from_icd11": "5A14", "icd10_code": "E141", "icd10_title": "" }, { "from_icd11": "5A14", "icd10_code": "E142", "icd10_title": "" }, { "from_icd11": "5A14", "icd10_code": "E143", "icd10_title": "" }, { "from_icd11": "5A14", "icd10_code": "E144", "icd10_title": "" }, { "from_icd11": "5A14", "icd10_code": "E145", "icd10_title": "" }, { "from_icd11": "5A14", "icd10_code": "E146", "icd10_title": "" }, { "from_icd11": "5A14", "icd10_code": "E147", "icd10_title": "" }, { "from_icd11": "5A14", "icd10_code": "E148", "icd10_title": "" }, { "from_icd11": "5A14", "icd10_code": "E149", "icd10_title": "" }, { "from_icd11": "JA63.2", "icd10_code": "O24420", "icd10_title": "Gestational diabetes mellitus in childbirth, diet controlled" }, { "from_icd11": "JA63.2", "icd10_code": "O24424", "icd10_title": "Gestational diabetes mellitus in childbirth, insulin controlled" }, { "from_icd11": "JA63.2", "icd10_code": "O24429", "icd10_title": "Gestational diabetes mellitus in childbirth, unspecified control" }, { "from_icd11": "JA63.2", "icd10_code": "O24410", "icd10_title": "Gestational diabetes mellitus in pregnancy, diet controlled" } ]
E14
Results: Twelve children (boys=7) received anakinra, dose 2-6 mg/kg, max 300mg/ day. All had received IVIG and pulse methylprednisolone (IVMP) 30 mg/kg/24h, 3-6 doses. Eight were admitted to ICU. In 5/8 anakinra was initiated concomitantly with IVIG and IVMP due to rapid deterioration of cardiovascular function, necessitating support with inotropes; in 3/8 due to non response to IVIG and IVMP. Three infants (all boys, aged 5-7 months) received anakinra for 6 months due to coronary involvement, 2 with Coronary Artery Aneurysms with improvement in a 1-month period, one with medium CA dilation with complete recovery. All other children were aged 5 to 14 years; 1 received anakinra for MAS resistant to 6 IVMP pulses, 8 for cardiovascular collapse. Median time to response in maximum anakinra dose was 2 days. All children had gastrointestinal involvement and four gallbladder edema; 2 developed pancreatitis that resolved after one month of treatment. In 7/9 older children duration of treatment with anakinra was 2 months and of steroids 1 month. A 13-year-old girl and an 11-year-old girl received anakinra for 6 months due to recalcitrant pericarditis and fever with hyperinflammation recurrence after URI, respectively. Except for the 2 infants with CAA all children recovered completely without sequelae. Cardiac MRI was performed 6 months after initial hospitalization and revealed normal cardiac function.
4.039063
0.63623
sec[0]/sec[242]/sec[0]/sec[0]/sec[0]/sec[0]/p[4]
en
0.999994
39252016
https://doi.org/10.1186/s12969-024-01004-z
[ "anakinra", "children", "ivmp", "ivig", "boys", "cardiovascular", "function", "response", "infants", "coronary" ]
[ { "code": "5B51&XS25", "title": "Marasmus in children" }, { "code": "5B7Z", "title": "Unspecified undernutrition" }, { "code": "5B51", "title": "Wasting in infants, children or adolescents" }, { "code": "5B53", "title": "Stunting in infants, children or adolescents" }, { "code": "DD93.Y", "title": "Other functional digestive disorders of infants, neonates or toddlers" }, { "code": "BE2Y", "title": "Other specified diseases of the circulatory system" }, { "code": "BE2Z", "title": "Diseases of the circulatory system, unspecified" }, { "code": "BA00.Z", "title": "Essential hypertension, unspecified" }, { "code": "BD1Z", "title": "Heart failure, unspecified" }, { "code": "5C56.0Y", "title": "Other specified sphingolipidosis" } ]
=== ICD-11 CODES FOUND === [5B7Z] Unspecified undernutrition Also known as: Unspecified undernutrition | Malnutrition NOS | nutritional deficiency NOS | nutritional depletion NOS | severe malnutrition NOS [5B51] Wasting in infants, children or adolescents Also known as: Wasting in infants, children or adolescents | Moderate wasting in infants, children or adolescents | moderate thinness in school-aged children and adolescents | Moderate acute undernutrition | Severe wasting in infants, children or adolescents [5B53] Stunting in infants, children or adolescents Also known as: Stunting in infants, children or adolescents | Moderate stunting in infants, children or adolescents | Moderate chronic undernutrition | Severe stunting in infants, children or adolescents | Severe chronic undernutrition [DD93.Y] Other functional digestive disorders of infants, neonates or toddlers Also known as: Other functional digestive disorders of infants, neonates or toddlers | Functional vomiting or aerophagia in childhood | Adolescent rumination syndrome | rumination syndrome in children | Cyclic vomiting syndrome in children [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 [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 [BA00.Z] Essential hypertension, unspecified Also known as: Essential hypertension, unspecified | Essential hypertension | idiopathic hypertension | primary hypertension | systemic primary arterial hypertension [BD1Z] Heart failure, unspecified Also known as: Heart failure, unspecified | myocardial failure | cardiac decompensation | cardiac failure | cardiac failure NOS [5C56.0Y] Other specified sphingolipidosis Also known as: Other specified sphingolipidosis | Mucolipidosis type 4 | Sialolipidosis | Gaucher disease | Acid beta-glucosidase deficiency === GRAPH WALKS === --- Walk 1 --- [5B7Z] Unspecified undernutrition --PARENT--> [?] Undernutrition Def: Undernutrition is a condition in which the body’s requirements are unmet due to underconsumption or to impaired absorption and use of nutrients. It can be produced by lack of access to food, or as a c... --CHILD--> [5B52] Acute malnutrition in infants, children or adolescents --- Walk 2 --- [5B7Z] Unspecified undernutrition --PARENT--> [?] Undernutrition Def: Undernutrition is a condition in which the body’s requirements are unmet due to underconsumption or to impaired absorption and use of nutrients. It can be produced by lack of access to food, or as a c... --EXCLUDES--> [?] Human immunodeficiency virus disease associated with wasting syndrome Def: This is a lentivirus (slowly replicating retrovirus) that causes acquired immunodeficiency syndrome (AIDS), a condition in humans in which progressive failure of the immune system allows life-threaten... --- Walk 3 --- [5B51] Wasting in infants, children or adolescents --PARENT--> [?] Undernutrition Def: Undernutrition is a condition in which the body’s requirements are unmet due to underconsumption or to impaired absorption and use of nutrients. It can be produced by lack of access to food, or as a c... --EXCLUDES--> [?] Intestinal malabsorption Def: Intestinal malabsorption (syndrome) occurs due to pathological interference with the normal physiological sequence of digestion (intraluminal process), absorption (mucosal process), and transport (pos... --- Walk 4 --- [5B51] Wasting in infants, children or adolescents --PARENT--> [?] Undernutrition Def: Undernutrition is a condition in which the body’s requirements are unmet due to underconsumption or to impaired absorption and use of nutrients. It can be produced by lack of access to food, or as a c... --EXCLUDES--> [?] Human immunodeficiency virus disease associated with wasting syndrome Def: This is a lentivirus (slowly replicating retrovirus) that causes acquired immunodeficiency syndrome (AIDS), a condition in humans in which progressive failure of the immune system allows life-threaten... --- Walk 5 --- [5B53] Stunting in infants, children or adolescents --PARENT--> [?] Undernutrition Def: Undernutrition is a condition in which the body’s requirements are unmet due to underconsumption or to impaired absorption and use of nutrients. It can be produced by lack of access to food, or as a c... --EXCLUDES--> [?] Effects of hunger --- Walk 6 --- [5B53] Stunting in infants, children or adolescents --PARENT--> [?] Undernutrition Def: Undernutrition is a condition in which the body’s requirements are unmet due to underconsumption or to impaired absorption and use of nutrients. It can be produced by lack of access to food, or as a c... --CHILD--> [5B50] Underweight in infants, children or adolescents
[ "[5B7Z] Unspecified undernutrition\n --PARENT--> [?] Undernutrition\n Def: Undernutrition is a condition in which the body’s requirements are unmet due to underconsumption or to impaired absorption and use of nutrients. It can be produced by lack of access to food, or as a c...\n --CHILD--> [5B52] Acute malnutrition in infants, children or adolescents", "[5B7Z] Unspecified undernutrition\n --PARENT--> [?] Undernutrition\n Def: Undernutrition is a condition in which the body’s requirements are unmet due to underconsumption or to impaired absorption and use of nutrients. It can be produced by lack of access to food, or as a c...\n --EXCLUDES--> [?] Human immunodeficiency virus disease associated with wasting syndrome\n Def: This is a lentivirus (slowly replicating retrovirus) that causes acquired immunodeficiency syndrome (AIDS), a condition in humans in which progressive failure of the immune system allows life-threaten...", "[5B51] Wasting in infants, children or adolescents\n --PARENT--> [?] Undernutrition\n Def: Undernutrition is a condition in which the body’s requirements are unmet due to underconsumption or to impaired absorption and use of nutrients. It can be produced by lack of access to food, or as a c...\n --EXCLUDES--> [?] Intestinal malabsorption\n Def: Intestinal malabsorption (syndrome) occurs due to pathological interference with the normal physiological sequence of digestion (intraluminal process), absorption (mucosal process), and transport (pos...", "[5B51] Wasting in infants, children or adolescents\n --PARENT--> [?] Undernutrition\n Def: Undernutrition is a condition in which the body’s requirements are unmet due to underconsumption or to impaired absorption and use of nutrients. It can be produced by lack of access to food, or as a c...\n --EXCLUDES--> [?] Human immunodeficiency virus disease associated with wasting syndrome\n Def: This is a lentivirus (slowly replicating retrovirus) that causes acquired immunodeficiency syndrome (AIDS), a condition in humans in which progressive failure of the immune system allows life-threaten...", "[5B53] Stunting in infants, children or adolescents\n --PARENT--> [?] Undernutrition\n Def: Undernutrition is a condition in which the body’s requirements are unmet due to underconsumption or to impaired absorption and use of nutrients. It can be produced by lack of access to food, or as a c...\n --EXCLUDES--> [?] Effects of hunger", "[5B53] Stunting in infants, children or adolescents\n --PARENT--> [?] Undernutrition\n Def: Undernutrition is a condition in which the body’s requirements are unmet due to underconsumption or to impaired absorption and use of nutrients. It can be produced by lack of access to food, or as a c...\n --CHILD--> [5B50] Underweight in infants, children or adolescents" ]
5B51&XS25
Marasmus in children
[ { "from_icd11": "5B7Z", "icd10_code": "E43", "icd10_title": "Unspecified severe protein-calorie malnutrition" }, { "from_icd11": "5B7Z", "icd10_code": "E538", "icd10_title": "Deficiency of other specified B group vitamins" }, { "from_icd11": "5B7Z", "icd10_code": "E569", "icd10_title": "Vitamin deficiency, unspecified" }, { "from_icd11": "5B7Z", "icd10_code": "E638", "icd10_title": "Other specified nutritional deficiencies" }, { "from_icd11": "5B7Z", "icd10_code": "E639", "icd10_title": "Nutritional deficiency, unspecified" }, { "from_icd11": "5B7Z", "icd10_code": "E41", "icd10_title": "Nutritional marasmus" }, { "from_icd11": "5B7Z", "icd10_code": "E539", "icd10_title": "Vitamin B deficiency, unspecified" }, { "from_icd11": "5B7Z", "icd10_code": "E568", "icd10_title": "Deficiency of other vitamins" }, { "from_icd11": "5B7Z", "icd10_code": "E649", "icd10_title": "Sequelae of unspecified nutritional deficiency" }, { "from_icd11": "5B7Z", "icd10_code": "E618", "icd10_title": "Deficiency of other specified nutrient elements" }, { "from_icd11": "5B7Z", "icd10_code": "E40-E46", "icd10_title": "" }, { "from_icd11": "5B7Z", "icd10_code": "E50-E64", "icd10_title": "" }, { "from_icd11": "5B7Z", "icd10_code": "E53", "icd10_title": "Deficiency of other B group vitamins" }, { "from_icd11": "5B7Z", "icd10_code": "E56", "icd10_title": "Other vitamin deficiencies" }, { "from_icd11": "5B7Z", "icd10_code": "E61", "icd10_title": "Deficiency of other nutrient elements" } ]
E43
Unspecified severe protein-calorie malnutrition
During following weeks there was a significant, life-threatening deterioration in the patient’s clinical condition (NEU – 0.0 10 3 /μl, Hb – 9.1 g/dl). Despite a lack of confirmation of the genetic diagnosis, due to the rapid deterioration of the patient’s condition, the medical council decided to implement non-standard treatment. Therefore, immunoablative treatment using anti-thymocyte globulins (ATG) (according to the SAA program) was implemented. A good response was achieved (the number of granulocytes increased to 74 x 10 3 /μl), but after 2 weeks the symptoms recurred. On Day 24 after ATG administration, the white blood cells (WBC) count dropped to 0.67 x 10 3 /μl. Due to the initial good response to ATG treatment, it was decided to start immunosuppressive treatment in accordance with the program for the treatment of HLH - dexamethasone, etoposide and cyclosporine. Improvement was achieved (WBC – 6.27 x 10 3 /μl) after 4 weeks of treatment. Due to persistent hypogammaglobulinemia, the patient received IVIG infusions. Then, for 11 months, the treatment according to the HLH 2004 regimen was continued, but it was complicated by the symptoms of renal failure (urea – 86 mg/dl), elevated N-terminal pro b-type natriuretic peptide – 34 130 pg/ml without clinical symptoms of heart failure and cytomegalovirus infection treated with ganciclovir. After 2 weeks of treatment, the virus was undetectable.
3.962891
0.972168
sec[1]/p[3]
en
0.999998
39624103
https://doi.org/10.3389/fimmu.2024.1484467
[ "deterioration", "decided", "according", "program", "good", "response", "failure", "life", "threatening", "despite" ]
[ { "code": "PL13.8", "title": "Expired or deteriorated medication or substance, as mode of injury or harm" }, { "code": "6A2Z", "title": "Schizophrenia or other primary psychotic disorders, unspecified" }, { "code": "BE2Y", "title": "Other specified diseases of the circulatory system" }, { "code": "MG20.Z", "title": "Cachexia, unspecified" }, { "code": "MG22", "title": "Fatigue" }, { "code": "QA47.Z", "title": "Liveborn infants according to place of birth, unspecified" }, { "code": "EE12.1", "title": "Onychomycosis" }, { "code": "QA00.5", "title": "Examination for normal comparison or control in clinical research programme" }, { "code": "4B40.2", "title": "Good syndrome" }, { "code": "6B24.0", "title": "Hoarding disorder with fair to good insight" } ]
=== 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 [6A2Z] Schizophrenia or other primary psychotic disorders, unspecified Also known as: Schizophrenia or other primary psychotic disorders, unspecified | Unspecified nonorganic psychosis | nonorganic psychosis | confusional psychosis | atypical psychosis [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 [MG20.Z] Cachexia, unspecified Also known as: Cachexia, unspecified | Cachexia | cachectic | general body deterioration | inanition [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 [QA47.Z] Liveborn infants according to place of birth, unspecified Also known as: Liveborn infants according to place of birth, unspecified | Liveborn infants according to place of birth [EE12.1] Onychomycosis Definition: Fungal infection of fingernails and/or toenails due most commonly to dermatophytes (tinea unguium) or yeasts, especially Candida species. Also known as: Onychomycosis | Fungal infection of the nails | Onychomycosis classified according to clinical pattern | Superficial white onychomycosis | Distal and lateral subungual onychomycosis Includes: Fungal infection of the nails Excludes: Candidosis of nail or paronychium [QA00.5] Examination for normal comparison or control in clinical research programme Also known as: Examination for normal comparison or control in clinical research programme | medical examination of control subject in clinical research [4B40.2] Good syndrome Definition: This is a condition that occurs in adults in whom hypogammaglobulinemia, deficient cell-mediated immunity, and benign thymoma may develop almost simultaneously. Also known as: Good syndrome | Thymoma immunodeficiency [6B24.0] Hoarding disorder with fair to good insight Definition: All definitional requirements of hoarding disorder are met. The individual recognizes that hoarding-related beliefs and behaviours (pertaining to excessive acquisition, difficulty discarding, or clutter) are problematic. This qualifier level may still be applied if, at circumscribed times (e.g., when being forced to discard items), the individual demonstrates no insight. Also known as: Hoarding disorder with fair to good insight === 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--> [PL13.2] Drug-related injury or harm in the context of correct administration or dosage, 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 --CHILD--> [PL13.0] Overdose of substance, as mode of injury or harm Def: Incorrect dose - too high... --- Walk 3 --- [6A2Z] Schizophrenia or other primary psychotic disorders, unspecified --PARENT--> [?] Schizophrenia or other primary psychotic disorders Def: Schizophrenia and other primary psychotic disorders are characterised by significant impairments in reality testing and alterations in behaviour manifest in positive symptoms such as persistent delusi... --RELATED_TO--> [?] 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... --- Walk 4 --- [6A2Z] Schizophrenia or other primary psychotic disorders, unspecified --PARENT--> [?] Schizophrenia or other primary psychotic disorders Def: Schizophrenia and other primary psychotic disorders are characterised by significant impairments in reality testing and alterations in behaviour manifest in positive symptoms such as persistent delusi... --PARENT--> [06] Mental, behavioural or neurodevelopmental disorders Def: Mental, behavioural and neurodevelopmental disorders are syndromes characterised by clinically significant disturbance in an individual's cognition, emotional regulation, or behaviour that reflects a ... --- Walk 5 --- [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--> [?] Functional vascular disorders of the skin Def: Skin disorders due to disturbances in vascular tone and skin blood flow.... --- 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... --RELATED_TO--> [?] Symptoms, signs or clinical findings of the circulatory system
[ "[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--> [PL13.2] Drug-related injury or harm in the context of correct administration or dosage, 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 --CHILD--> [PL13.0] Overdose of substance, as mode of injury or harm\n Def: Incorrect dose - too high...", "[6A2Z] Schizophrenia or other primary psychotic disorders, unspecified\n --PARENT--> [?] Schizophrenia or other primary psychotic disorders\n Def: Schizophrenia and other primary psychotic disorders are characterised by significant impairments in reality testing and alterations in behaviour manifest in positive symptoms such as persistent delusi...\n --RELATED_TO--> [?] 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...", "[6A2Z] Schizophrenia or other primary psychotic disorders, unspecified\n --PARENT--> [?] Schizophrenia or other primary psychotic disorders\n Def: Schizophrenia and other primary psychotic disorders are characterised by significant impairments in reality testing and alterations in behaviour manifest in positive symptoms such as persistent delusi...\n --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 ...", "[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--> [?] Functional vascular disorders of the skin\n Def: Skin disorders due to disturbances in vascular tone and skin blood flow....", "[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--> [?] Symptoms, signs or clinical findings of the circulatory system" ]
PL13.8
Expired or deteriorated medication or substance, as mode of injury or harm
[ { "from_icd11": "6A2Z", "icd10_code": "F29", "icd10_title": "Unspecified psychosis not due to a substance or known physiological condition" }, { "from_icd11": "6A2Z", "icd10_code": "F28", "icd10_title": "Other psychotic disorder not due to a substance or known physiological condition" }, { "from_icd11": "6A2Z", "icd10_code": "F20-F29", "icd10_title": "" }, { "from_icd11": "6A2Z", "icd10_code": "F204", "icd10_title": "" }, { "from_icd11": "MG20.Z", "icd10_code": "R627", "icd10_title": "Adult failure to thrive" }, { "from_icd11": "MG20.Z", "icd10_code": "R64", "icd10_title": "Cachexia" }, { "from_icd11": "MG22", "icd10_code": "R5382", "icd10_title": "Chronic fatigue, unspecified" }, { "from_icd11": "MG22", "icd10_code": "R530", "icd10_title": "Neoplastic (malignant) related fatigue" }, { "from_icd11": "MG22", "icd10_code": "R532", "icd10_title": "Functional quadriplegia" }, { "from_icd11": "MG22", "icd10_code": "R531", "icd10_title": "Weakness" }, { "from_icd11": "MG22", "icd10_code": "R5383", "icd10_title": "Other fatigue" }, { "from_icd11": "MG22", "icd10_code": "R53", "icd10_title": "Malaise and fatigue" }, { "from_icd11": "QA47.Z", "icd10_code": "Z38", "icd10_title": "Liveborn infants according to place of birth and type of delivery" }, { "from_icd11": "QA47.Z", "icd10_code": "Z388", "icd10_title": "Other multiple liveborn infant, unspecified as to place of birth" }, { "from_icd11": "QA00.5", "icd10_code": "Z006", "icd10_title": "Encounter for examination for normal comparison and control in clinical research program" } ]
F29
Unspecified psychosis not due to a substance or known physiological condition
Here, we present 2 siblings born to healthy, consanguineous first-cousin parents from Sudan . In addition, there was one spontaneous termination of pregnancy for which information was not available. The proband (P1) is a male who presented with ataxia and severe global developmental delay. The pregnancy and delivery history were uneventful. At 3 years of age, he was hypotonic and areflexic, and lacked head control. He was unable to crawl or speak. By 8 years of age, he had dysarthria, nystagmus, and dysmetria, with greater interest in his surroundings, and ambulation with unilateral support. Hearing and vision remained intact. Further examination revealed microcephaly, spasticity, and hyperreflexia of both upper and lower limbs, in addition to feet deformity. Brain MRI showed a mildly thinned corpus callosum and mildly dilated lateral ventricles , but the cerebellum was intact. The diffusion-weighted imaging (DWI) sequences showed bilateral symmetric hyperintensities in the posterior limbs of the internal capsules . His younger sister (P2) presented also with delayed milestones. At 4 years old, she had dysarthria, and she could walk with support. Microcephaly, nystagmus, and spasticity of upper and lower limbs were present, but there was no ataxia. MRI of the brain showed a thinned corpus callosum and bilateral symmetric DWI hyperintense signals in the posterior limbs of the internal capsules .
4.03125
0.963379
sec[2]/sec[0]/p[0]
en
0.999996
39066872
https://doi.org/10.1007/s10048-024-00773-9
[ "limbs", "present", "addition", "pregnancy", "ataxia", "dysarthria", "nystagmus", "support", "intact", "microcephaly" ]
[ { "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": "JA82.2", "title": "Maternal care for transverse or oblique lie" }, { "code": "JA82.1", "title": "Maternal care for breech presentation" }, { "code": "JA82.Z", "title": "Maternal care for malpresentation of fetus, unspecified" }, { "code": "JA82.6", "title": "Maternal care for compound presentation" }, { "code": "JA82.5", "title": "Maternal care for multiple gestation with malpresentation of one fetus or more" } ]
=== 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 [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 [JA82.1] Maternal care for breech presentation Also known as: Maternal care for breech presentation | breech fetal presentation | breech presentation | malposition of fetus in breech presentation | positions of breech presentation [JA82.Z] Maternal care for malpresentation of fetus, unspecified Also known as: Maternal care for malpresentation of fetus, unspecified | Maternal care for malpresentation of fetus | abnormal fetal presentation | malpresentation of fetus | fetal malpresentation [JA82.6] Maternal care for compound presentation Also known as: Maternal care for compound presentation | compound presentation of fetus [JA82.5] Maternal care for multiple gestation with malpresentation of one fetus or more Also known as: Maternal care for multiple gestation with malpresentation of one fetus or more | abnormal presentation in multiple gestation === GRAPH WALKS === --- Walk 1 --- [ND56.1] Open wound of unspecified body region --PARENT--> [ND56] Injury of unspecified body region Def: Damage inflicted on the body in an unspecified area as the direct or indirect result of an external force, with or without disruption of structural continuity.... --CHILD--> [ND56.2] Fracture of unspecified body region --- Walk 2 --- [ND56.1] Open wound of unspecified body region --PARENT--> [ND56] Injury of unspecified body region Def: Damage inflicted on the body in an unspecified area as the direct or indirect result of an external force, with or without disruption of structural continuity.... --CHILD--> [ND56.0] Superficial injury 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--> [LB72] Structural developmental anomalies of shoulder girdle Def: Any condition caused by failure of the shoulder girdle to correctly develop during the antenatal period.... --- Walk 4 --- [LB9Z] Structural developmental anomalies of the skeleton, unspecified --PARENT--> [?] Structural developmental anomalies of the skeleton Def: A deformation established before birth of an anatomical structure of one or more bones.... --CHILD--> [LB71] Structural developmental anomalies of facial bones Def: Any condition caused by failure of the facial bones to correctly develop during the antenatal period.... --- Walk 5 --- [FB56.6] Other specified soft tissue disorders --PARENT--> [FB56] Specified soft tissue disorders, not elsewhere classified Def: This is a group of other disorders, which are not classified elsewhere, affecting tissues that connect, support, or surround other structures and organs of the body, not being bone.... --EXCLUDES--> [?] Mononeuropathy --- 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--> [?] Radiculopathy
[ "[ND56.1] Open wound of unspecified body region\n --PARENT--> [ND56] Injury of unspecified body region\n Def: Damage inflicted on the body in an unspecified area as the direct or indirect result of an external force, with or without disruption of structural continuity....\n --CHILD--> [ND56.2] Fracture of unspecified body region", "[ND56.1] Open wound of unspecified body region\n --PARENT--> [ND56] Injury of unspecified body region\n Def: Damage inflicted on the body in an unspecified area as the direct or indirect result of an external force, with or without disruption of structural continuity....\n --CHILD--> [ND56.0] Superficial injury 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--> [LB72] Structural developmental anomalies of shoulder girdle\n Def: Any condition caused by failure of the shoulder girdle to correctly develop during the antenatal period....", "[LB9Z] Structural developmental anomalies of the skeleton, unspecified\n --PARENT--> [?] Structural developmental anomalies of the skeleton\n Def: A deformation established before birth of an anatomical structure of one or more bones....\n --CHILD--> [LB71] Structural developmental anomalies of facial bones\n Def: Any condition caused by failure of the facial bones to correctly develop during the antenatal period....", "[FB56.6] Other specified soft tissue disorders\n --PARENT--> [FB56] Specified soft tissue disorders, not elsewhere classified\n Def: This is a group of other disorders, which are not classified elsewhere, affecting tissues that connect, support, or surround other structures and organs of the body, not being bone....\n --EXCLUDES--> [?] Mononeuropathy", "[FB56.6] Other specified soft tissue disorders\n --PARENT--> [FB56] Specified soft tissue disorders, not elsewhere classified\n Def: This is a group of other disorders, which are not classified elsewhere, affecting tissues that connect, support, or surround other structures and organs of the body, not being bone....\n --EXCLUDES--> [?] Radiculopathy" ]
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
The laboratory findings revealed several significant abnormalities. The hemoglobin level was 11.3 g/dL (normal range: 12.0-16.0 g/dL). The platelet count was within normal limits at 182,000/μL (normal range: 150,000-450,000/μL). However, both aspartate aminotransferase (ASAT) and alanine aminotransferase (ALAT) were markedly elevated. ASAT was 8 times above the normal range, while ALAT was 4 times elevated (normal range: ASAT 10-40 U/L, ALAT 7-56 U/L). The prothrombin time was reduced to 55%, below the normal range of 70%-100%. Potassium levels were found to be low at 3.2 mmol/L (normal range: 3.5-5.0 mmol/L), and creatinine was significantly elevated at 10.82 mg/dL (normal range: 0.6-1.2 mg/dL). Urea levels were 0.43 g/dL (normal range: 0.7-1.2 g/dL). Arterial blood gas analysis revealed a pH of 7.54, indicative of metabolic alkalosis (normal range: 7.35-7.45). The partial pressure of oxygen (PaO2) was elevated at 148 mmHg, exceeding the normal range of 75-100 mmHg. The partial pressure of carbon dioxide (PaCO2) was low at 6.1 mmHg (normal range: 35-45 mmHg), suggesting respiratory alkalosis. The bicarbonate (HCO3-) level was low at 6.1 mmol/L (normal range: 22-28 mmol/L), and lactate levels were elevated at 7.9 mmol/L, indicating hyperlactatemia (normal range: 0.5-2.2 mmol/L). Additionally, proteinuria was present, with a level of 900 mg/mL, significantly above the normal range of <150 mg/mL.
4.277344
0.553711
sec[1]/p[1]
en
0.999996
39850765
https://doi.org/10.1016/j.radcr.2024.12.018
[ "range", "mmol", "mmhg", "asat", "alat", "aminotransferase", "times", "significantly", "alkalosis", "partial" ]
[ { "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": "GB42.1", "title": "Albuminuria, Grade A3" }, { "code": "GB42.0", "title": "Albuminuria, Grade A2" }, { "code": "MA18.0Y", "title": "Other specified elevated blood glucose level" }, { "code": "5C50.9", "title": "Disorders of ornithine metabolism" }, { "code": "5C50.12", "title": "Tyrosinaemia type 2" } ]
=== 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 [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 [5C50.9] Disorders of ornithine metabolism Also known as: Disorders of ornithine metabolism | Hyperornithinaemia | Ornithinaemia | Ornithine aminotransferase deficiency | Generalised gyrate choroid atrophy [5C50.12] Tyrosinaemia type 2 Definition: Tyrosinemia type 2 is an inborn error of tyrosine metabolism characterised by hypertyrosinemia with oculocutaneous manifestations (eye redness, photophobia, excessive tearing and pain, palmoplantar hyperkeratosis) and, in some cases, intellectual deficit. Also known as: Tyrosinaemia type 2 | Hepatic tyrosine aminotransferase deficiency | Tyrosine transaminase deficiency | Keratosis palmoplantaris - corneal dystrophy | Oculocutaneous tyrosinaemia === GRAPH WALKS === --- Walk 1 --- [QA00.6Y] Other specified examination of eyes or vision --PARENT--> [QA00.6] Examination of eyes or vision --PARENT--> [QA00] General examination or investigation of persons without complaint or reported diagnosis --- Walk 2 --- [QA00.6Y] Other specified examination of eyes or vision --PARENT--> [QA00.6] Examination of eyes or vision --CHILD--> [QA00.6Y] Other specified examination of eyes or vision --- Walk 3 --- [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 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--> [3B63.1Y] 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 --PARENT--> [QA00] General examination or investigation of persons without complaint or reported diagnosis", "[QA00.6Y] Other specified examination of eyes or vision\n --PARENT--> [QA00.6] Examination of eyes or vision\n --CHILD--> [QA00.6Y] Other specified examination of eyes or vision", "[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....", "[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--> [3B63.1Y] 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": "5C50.9", "icd10_code": "E724", "icd10_title": "Disorders of ornithine metabolism" } ]
D473
Essential (hemorrhagic) thrombocythemia
A 46-year-old man (BSA 1.92 m 2 ; BMI 24.5 Kg/m 2 ) without previous cardiovascular events, who was affected by anti-Mi2 dermatomyositis and lymphocytic interstitial pneumonia (LIP) with chronic respiratory failure and was treated with 50 mg of azathioprine daily, 25 mg prednisone daily, 700 mg of intravenous (IV) rituximab once weekly, and oxygen therapy (1 to 6 L per minute), was admitted to the Emergency Department (ED) of our institution due to ongoing dyspnoea, chest pain, and general malaise. At the hospital admission, the patient’s arterial oxygen saturation (SaO2) in ambient air was 66%, their blood pressure was 110/70 mmHg, their heart rate was 102 b.p.m., and their body temperature was 36.3 °C. A blood gas analysis showed hypoxemia (PaO2 = 39.6 mmHg) and hypocapnia (PaCO2 = 27.2 mmHg), pH = 7.3, and a lactate level of 7.7 mmol/L (normal range: 0.36–1.25 mmol/L). Blood tests revealed a serum haemoglobin amount of 12.8 g/dL; a serum white blood cell count of 13,900 × 10 6 /L ; a serum Neutrophil–Lymphocyte Ratio (NLR) of 18.6; a serum creatinine level of 1.57 mg/dL; a serum troponin I level of 0.42 ng/mL (normal range 0.00–0.04 ng/mL); a serum C-reactive protein (CRP) amount of 58 mg/L (normal range: 0–5 mg/L); a serum D-dimer of 4215 microg/L (normal range: 1–500 microg/L); and a serum N-terminal pro-B-type natriuretic peptide (NT-proBNP) level of 6474 pg/mL (normal range: <125 pg/mL).
4.019531
0.97168
sec[1]/p[0]
en
0.999998
PMC11942914
https://doi.org/10.3390/jcm14062035
[ "serum", "range", "blood", "their", "mmhg", "daily", "oxygen", "mmol", "microg", "without" ]
[ { "code": "NE80.3", "title": "Other serum reactions" }, { "code": "5D0Y", "title": "Other specified metabolic disorders" }, { "code": "5B91.0", "title": "Hypercalcaemia" }, { "code": "4A84.Y", "title": "Other specified anaphylaxis" }, { "code": "5C50.F2", "title": "Homocarnosinosis" }, { "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 === [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 [5B91.0] Hypercalcaemia Definition: Hypercalcaemia is a condition caused by increased calcium levels. The higher the calcium levels and the faster its level rises, the more severe will be the symptoms. When present, symptoms are caused by dehydration secondary to urinary losses of calcium, water and other electrolytes, and to an increase in membrane potential caused by the elevation in extracellular fluid ionized calcium concentration. Patients with moderate to severe hypercalcaemia often complain of nausea and vomiting, symptoms Also known as: Hypercalcaemia | Calcium excess | elevated serum calcium | hypercalcaemic crisis | hypercalcaemic syndrome [4A84.Y] Other specified anaphylaxis Also known as: Other specified anaphylaxis | Latex-induced anaphylaxis | Anaphylaxis due to latex | Latex anaphylaxis | Anaphylactic shock due to serum [5C50.F2] Homocarnosinosis Definition: Homocarnosinosis is a metabolic defect characterised by progressive spastic diplegia, intellectual deficit and retinitis pigmentosa. This extremely rare disorder has been reported in only one family, namely a woman and three of her children. The latter showed but their mother was symptom free. It is therefore uncertain whether there is a relationship between the biochemical defect and the clinical symptoms. Inheritance in the reported family seems to be autosomal dominant. Also known as: Homocarnosinosis | Homocarnosinase deficiency | Serum carnosinase deficiency [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 --- [NE80.3] Other serum reactions --RELATED_TO--> [?] Serum sickness vasculitis Def: An acute vasculitic illness typified by fever, arthralgia and urticarial vasculitis resulting from an immune complex-mediated (type III) immune reaction to foreign protein. Historically this was large... --PARENT--> [?] Vasculitis associated with probable aetiology Def: Vasculitis that is associated with a probable specific etiology. The name (diagnosis) should have a prefix term specifying the association (e.g. hydralazine-associated microscopic polyangiitis, hepati... --- Walk 2 --- [NE80.3] Other serum reactions --RELATED_TO--> [?] Anaphylactic shock due to serum --PARENT--> [?] Anaphylaxis Def: Anaphylaxis is a severe, life-threatening systemic hypersensitivity reaction characterised by being rapid in onset with potentially life-threatening airway, breathing, or circulatory problems and is u... --- Walk 3 --- [5D0Y] Other specified metabolic disorders --PARENT--> [?] Other metabolic disorders --CHILD--> [5D00] Amyloidosis Def: Amyloidosis is a vast group of diseases defined by the presence of insoluble protein deposits in tissues. Its diagnosis is based on histological findings. Amyloidoses are classified according to clini... --- Walk 4 --- [5D0Y] Other specified metabolic disorders --PARENT--> [?] Other metabolic disorders --CHILD--> [5D00] Amyloidosis Def: Amyloidosis is a vast group of diseases defined by the presence of insoluble protein deposits in tissues. Its diagnosis is based on histological findings. Amyloidoses are classified according to clini... --- Walk 5 --- [5B91.0] Hypercalcaemia Def: Hypercalcaemia is a condition caused by increased calcium levels. The higher the calcium levels and the faster its level rises, the more severe will be the symptoms. When present, symptoms are caused ... --RELATED_TO--> [?] Myopathy due to hypercalcaemia --PARENT--> [?] Neurological disorders due to an excess of micro or macro nutrients --- Walk 6 --- [5B91.0] Hypercalcaemia Def: Hypercalcaemia is a condition caused by increased calcium levels. The higher the calcium levels and the faster its level rises, the more severe will be the symptoms. When present, symptoms are caused ... --PARENT--> [5B91] Mineral excesses --CHILD--> [5B91.1] Zinc excess Def: Adverse effects associated with chronic intake of supplemental zinc include suppression of immune response, decrease in high-density lipoprotein (HDL) cholesterol and reduced copper status. Acute adve...
[ "[NE80.3] Other serum reactions\n --RELATED_TO--> [?] Serum sickness vasculitis\n Def: An acute vasculitic illness typified by fever, arthralgia and urticarial vasculitis resulting from an immune complex-mediated (type III) immune reaction to foreign protein. Historically this was large...\n --PARENT--> [?] Vasculitis associated with probable aetiology\n Def: Vasculitis that is associated with a probable specific etiology. The name (diagnosis) should have a prefix term specifying the association (e.g. hydralazine-associated microscopic polyangiitis, hepati...", "[NE80.3] Other serum reactions\n --RELATED_TO--> [?] Anaphylactic shock due to serum\n --PARENT--> [?] Anaphylaxis\n Def: Anaphylaxis is a severe, life-threatening systemic hypersensitivity reaction characterised by being rapid in onset with potentially life-threatening airway, breathing, or circulatory problems and is u...", "[5D0Y] Other specified metabolic disorders\n --PARENT--> [?] Other metabolic disorders\n --CHILD--> [5D00] Amyloidosis\n Def: Amyloidosis is a vast group of diseases defined by the presence of insoluble protein deposits in tissues. Its diagnosis is based on histological findings. Amyloidoses are classified according to clini...", "[5D0Y] Other specified metabolic disorders\n --PARENT--> [?] Other metabolic disorders\n --CHILD--> [5D00] Amyloidosis\n Def: Amyloidosis is a vast group of diseases defined by the presence of insoluble protein deposits in tissues. Its diagnosis is based on histological findings. Amyloidoses are classified according to clini...", "[5B91.0] Hypercalcaemia\n Def: Hypercalcaemia is a condition caused by increased calcium levels. The higher the calcium levels and the faster its level rises, the more severe will be the symptoms. When present, symptoms are caused ...\n --RELATED_TO--> [?] Myopathy due to hypercalcaemia\n --PARENT--> [?] Neurological disorders due to an excess of micro or macro nutrients", "[5B91.0] Hypercalcaemia\n Def: Hypercalcaemia is a condition caused by increased calcium levels. The higher the calcium levels and the faster its level rises, the more severe will be the symptoms. When present, symptoms are caused ...\n --PARENT--> [5B91] Mineral excesses\n --CHILD--> [5B91.1] Zinc excess\n Def: Adverse effects associated with chronic intake of supplemental zinc include suppression of immune response, decrease in high-density lipoprotein (HDL) cholesterol and reduced copper status. Acute adve..." ]
NE80.3
Other serum reactions
[ { "from_icd11": "NE80.3", "icd10_code": "T880XXA", "icd10_title": "Infection following immunization, initial encounter" }, { "from_icd11": "NE80.3", "icd10_code": "T8061XA", "icd10_title": "Other serum reaction due to administration of blood and blood products, initial encounter" }, { "from_icd11": "NE80.3", "icd10_code": "T8069XA", "icd10_title": "Other serum reaction due to other serum, initial encounter" }, { "from_icd11": "NE80.3", "icd10_code": "T8062XA", "icd10_title": "Other serum reaction due to vaccination, initial encounter" }, { "from_icd11": "NE80.3", "icd10_code": "T806", "icd10_title": "Other serum reactions" }, { "from_icd11": "NE80.3", "icd10_code": "T880", "icd10_title": "Infection following immunization" }, { "from_icd11": "5C50.F2", "icd10_code": "E7281", "icd10_title": "Disorders of gamma aminobutyric acid metabolism" }, { "from_icd11": "5C50.F2", "icd10_code": "E728", "icd10_title": "Other specified disorders of amino-acid metabolism" }, { "from_icd11": "3B63.1Z", "icd10_code": "D473", "icd10_title": "Essential (hemorrhagic) thrombocythemia" }, { "from_icd11": "MA14.1C", "icd10_code": "R760", "icd10_title": "Raised antibody titer" } ]
T880XXA
Infection following immunization, initial encounter
Drug-induced urinary calculi are rare. Previous studies reported that ceftriaxone, a ceftriaxone drug, can cause urinary calculi. The mechanism may involve the binding of ceftriaxone to calcium ions, leading to the formation of crystals that closely adhere to the surface of renal tubule cells, thereby blocking renal tubules, damaging cells, and interfering with calcium reabsorption. The increased calcium level in the urine continues to bind to ceftriaxone and form more crystals. Although ceftazidime causes urinary calculi, only 1 study reported that calculi disappeared after the insertion of a double J-type ureteral stent during surgery and the cessation of intravenous injection of ceftazidime and potassium sodium hydrogen citrate particles to alkalize the urine. The patient underwent laparoscopic appendectomy due to acute appendicitis. Preoperative CT revealed no urinary calculi, and the patient only received only anti-infection treatment with ceftazidime without any other drug injection or drug administration, The patient had no metabolic disorders, malnutrition or other diseases. Therefore, we believe that the calculi in the right kidney and ureter of the patient were caused by ceftazidime. In addition, we refer to the treatment plan of ceftriaxone causing urinary calculi and recommend ceftazidime drug discontinuation, spasmolytic treatment, and hydration treatment before calculus discharge.
4.082031
0.749023
sec[2]/p[0]
en
0.999998
40258730
https://doi.org/10.1097/MD.0000000000042221
[ "calculi", "drug", "urinary", "ceftriaxone", "ceftazidime", "that", "calcium", "crystals", "renal", "cells" ]
[ { "code": "GB70.Z", "title": "Calculus of upper urinary tract, unspecified" }, { "code": "GB71.0", "title": "Calculus in bladder" }, { "code": "CB40.Y", "title": "Other specified diseases of the respiratory system" }, { "code": "GB70.0Z", "title": "Calculus of kidney, unspecified" }, { "code": "DC11.3", "title": "Calculus of gallbladder or cystic duct without cholecystitis or cholangitis" }, { "code": "QE11.Z", "title": "Hazardous drug use, unspecified" }, { "code": "6C4G.2Z", "title": "Unknown or unspecified psychoactive substance dependence, substance and state of remission unspecified" }, { "code": "NE60", "title": "Harmful effects of drugs, medicaments or biological substances, not elsewhere classified" }, { "code": "4A85.0Z", "title": "Drug hypersensitivity of unspecified type" }, { "code": "6C4G.3", "title": "Intoxication due to unknown or unspecified psychoactive substance" } ]
=== ICD-11 CODES FOUND === [GB70.Z] Calculus of upper urinary tract, unspecified Also known as: Calculus of upper urinary tract, unspecified | Calculus of upper urinary tract | calculus of urinary tract NOS | urinary calculi | urinary calculus, unspecified [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) [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 [GB70.0Z] Calculus of kidney, unspecified Also known as: Calculus of kidney, unspecified | Calculus of kidney | Renal calculus or stone | Stone in kidney | kidney calculi [DC11.3] Calculus of gallbladder or cystic duct without cholecystitis or cholangitis Definition: Stones in gallbladder present without inflammation of the gall bladder wall and bile duct. Also known as: Calculus of gallbladder or cystic duct without cholecystitis or cholangitis | cholesterol calculi | cholesterol calculus | Cholelithiasis unspecified and without cholecystitis or cholangitis | calculous disease of gallbladder [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 [6C4G.2Z] Unknown or unspecified psychoactive substance dependence, substance and state of remission unspecified Also known as: Unknown or unspecified psychoactive substance dependence, substance and state of remission unspecified | Unknown or unspecified psychoactive substance dependence | Drug dependence 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 [4A85.0Z] Drug hypersensitivity of unspecified type Also known as: Drug hypersensitivity of unspecified type | Drug or pharmacological agents hypersensitivity | medicinal hypersensitivity | drug sensitivity NOS [6C4G.3] Intoxication due to unknown or unspecified psychoactive substance Definition: Intoxication due to unknown or unspecified psychoactive substance is a transient condition that develops during or shortly after the administration of an unknown or unspecified psychoactive substance that is characterised by disturbances in level of consciousness, cognition, perception, affect or behaviour, or other psychophysiological functions and responses. This diagnosis should be made only when there is strong evidence that an unidentified substance has been taken and the features cannot be Also known as: Intoxication due to unknown or unspecified psychoactive substance | psychoactive substance abuse | trance and possession disorders in psychoactive substance intoxication | drug intoxication NOS === GRAPH WALKS === --- Walk 1 --- [GB70.Z] Calculus of upper urinary tract, unspecified --PARENT--> [GB70] Calculus of upper urinary tract Def: A condition of the urinary system, caused by dehydration, decreased urine volume or fluid flow rates, or increased excretion of minerals such as calcium, oxalate, magnesium, cystine, and phosphate. Th... --PARENT--> [?] Urolithiasis Def: A condition of the urinary system, caused by dehydration, decreased urine volume or fluid flow rates, or increased excretion of minerals such as calcium, oxalate, magnesium, cystine, and phosphate. Th... --- Walk 2 --- [GB70.Z] Calculus of upper urinary tract, unspecified --PARENT--> [GB70] 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--> [GB70.Z] Calculus of upper urinary tract, unspecified --- Walk 3 --- [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... --- Walk 4 --- [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 5 --- [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 6 --- [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...
[ "[GB70.Z] Calculus of upper urinary tract, unspecified\n --PARENT--> [GB70] Calculus of upper urinary tract\n Def: A condition of the urinary system, caused by dehydration, decreased urine volume or fluid flow rates, or increased excretion of minerals such as calcium, oxalate, magnesium, cystine, and phosphate. Th...\n --PARENT--> [?] Urolithiasis\n Def: A condition of the urinary system, caused by dehydration, decreased urine volume or fluid flow rates, or increased excretion of minerals such as calcium, oxalate, magnesium, cystine, and phosphate. Th...", "[GB70.Z] Calculus of upper urinary tract, unspecified\n --PARENT--> [GB70] 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--> [GB70.Z] Calculus of upper urinary tract, unspecified", "[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...", "[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", "[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--> [?] 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..." ]
GB70.Z
Calculus of upper urinary tract, unspecified
[ { "from_icd11": "GB70.Z", "icd10_code": "N202", "icd10_title": "Calculus of kidney with calculus of ureter" }, { "from_icd11": "GB70.Z", "icd10_code": "N209", "icd10_title": "Urinary calculus, unspecified" }, { "from_icd11": "GB70.Z", "icd10_code": "N20", "icd10_title": "Calculus of kidney and ureter" }, { "from_icd11": "GB71.0", "icd10_code": "N210", "icd10_title": "Calculus in bladder" }, { "from_icd11": "GB70.0Z", "icd10_code": "N200", "icd10_title": "Calculus of kidney" }, { "from_icd11": "DC11.3", "icd10_code": "K8021", "icd10_title": "Calculus of gallbladder without cholecystitis with obstruction" }, { "from_icd11": "DC11.3", "icd10_code": "K8020", "icd10_title": "Calculus of gallbladder without cholecystitis without obstruction" }, { "from_icd11": "DC11.3", "icd10_code": "K802", "icd10_title": "Calculus of gallbladder without cholecystitis" }, { "from_icd11": "QE11.Z", "icd10_code": "Z722", "icd10_title": "" }, { "from_icd11": "6C4G.2Z", "icd10_code": "F1920", "icd10_title": "Other psychoactive substance dependence, uncomplicated" }, { "from_icd11": "6C4G.2Z", "icd10_code": "F19239", "icd10_title": "Other psychoactive substance dependence with withdrawal, unspecified" }, { "from_icd11": "6C4G.2Z", "icd10_code": "F1921", "icd10_title": "Other psychoactive substance dependence, in remission" }, { "from_icd11": "6C4G.2Z", "icd10_code": "F19221", "icd10_title": "Other psychoactive substance dependence with intoxication delirium" }, { "from_icd11": "6C4G.2Z", "icd10_code": "F1924", "icd10_title": "Other psychoactive substance dependence with psychoactive substance-induced mood disorder" }, { "from_icd11": "6C4G.2Z", "icd10_code": "F19229", "icd10_title": "Other psychoactive substance dependence with intoxication, unspecified" } ]
N202
Calculus of kidney with calculus of ureter
A 3-month-old male infant, 5.35 kg, was diagnosed with severe MS and MR via transthoracic echocardiography . Preoperative echocardiography revealed right heart and left atrial enlargement, with the left ventricle compressed into a “D” shape. The mitral valve is significantly thickened, with hypertrophic and underdeveloped papillary muscles and thickened, shortened chordae tendineae. The valve leaflets are stiff, with restricted opening (orifice area −1.0 cm 2 ) and poor closure. The tricuspid valve is also thickened, with thickened and shortened sub-valvular chordae tendineae and poor closure. Color Doppler flow imaging (CDFI) revealed accelerated diastolic blood flow through the mitral valve with a peak velocity of 2.7 m/s, a pressure gradient of 29 mmHg, and a mean pressure gradient of 13 mmHg. Significant regurgitation signals are observed on the left atrial side during systole for the mitral valve and on the right atrial side during systole for the tricuspid valve. To address these conditions, the patient underwent a complex mitral valvuloplasty procedure under anesthesia . The mitral valve repair procedure includes several key steps: firstly, the abnormal chordae tendineae are excised, followed by commissurotomy and papillary muscle release. Subsequently, artificial chordae tendineae are placed, and repair is performed using the commissure magic stitch technique ( Supplementary Video S1 ).
4.144531
0.92627
sec[1]/p[0]
en
0.999996
39114560
https://doi.org/10.3389/fcvm.2024.1425900
[ "valve", "mitral", "thickened", "chordae", "tendineae", "atrial", "echocardiography", "papillary", "shortened", "poor" ]
[ { "code": "GB61.Z", "title": "Chronic kidney disease, stage unspecified" }, { "code": "BC00", "title": "Multiple valve disease" }, { "code": "BB9Z", "title": "Pulmonary valve disease, unspecified" }, { "code": "BB6Z", "title": "Mitral valve disease, unspecified" }, { "code": "LA8Z", "title": "Structural developmental anomaly of heart or great vessels, unspecified" }, { "code": "BB60.Z", "title": "Mitral valve stenosis, unspecified" }, { "code": "LA89.2", "title": "Mitral atresia" }, { "code": "LA87.11", "title": "Congenital mitral valvar stenosis" }, { "code": "LA87.10", "title": "Congenital mitral regurgitation" }, { "code": "FB86.11", "title": "Hypertrophy of bone" } ]
=== ICD-11 CODES FOUND === [GB61.Z] Chronic kidney disease, stage unspecified Also known as: Chronic kidney disease, stage unspecified | Chronic kidney disease | chronic renal failure | chronic kidney failure | chronic renal disease [BC00] Multiple valve disease Also known as: Multiple valve disease | Multiple valve disease of unspecified origin | multiple valvular cardiac dysfunction | multivalvular cardiac dysfunction | Disorders of both mitral and aortic valves [BB9Z] Pulmonary valve disease, unspecified Also known as: Pulmonary valve disease, unspecified | rheumatic heart disease of pulmonary valve, unspecified | chronic rheumatic pulmonary valve endocarditis | chronic rheumatic pulmonary valvular endocarditis | rheumatic disease of pulmonary valve [BB6Z] Mitral valve disease, unspecified Also known as: Mitral valve disease, unspecified | noninfective endocarditis of mitral valve | rheumatic heart disease of mitral valve, unspecified | mitral valvulopathy | mitral valve cardiopathy [LA8Z] Structural developmental anomaly of heart or great vessels, unspecified Also known as: Structural developmental anomaly of heart or great vessels, unspecified | Heart malformations | Cardiac malformations | congenital anomaly of heart | congenital heart disease [BB60.Z] Mitral valve stenosis, unspecified Also known as: Mitral valve stenosis, unspecified | Mitral valve stenosis | MS - [mitral stenosis] | mitral stenosis | mitral valvular stricture [LA89.2] Mitral atresia Definition: A congenital cardiovascular malformation with absence of the mitral valvar annulus (connection/junction) or an imperforate mitral valve. Also known as: Mitral atresia | Mitral atresia with absent atrioventricular connection | absent left atrioventricular connection or junction | absent left atrioventricular connection in laevocardia | mitral atresia with absent valvar annulus [LA87.11] Congenital mitral valvar stenosis Definition: A congenital cardiovascular malformation of the mitral valve in which there is narrowing or stricture of the valvar orifice (obstruction to flow). Also known as: Congenital mitral valvar stenosis | Duroziez disease | congenital mitral stenosis | congenital stenosis of mitral valve | congenital mitral valve stricture [LA87.10] Congenital mitral regurgitation Definition: A congenital cardiovascular finding in which there is backward flow through the mitral valve. Also known as: Congenital mitral regurgitation | congenital insufficiency of mitral valve | congenital mitral insufficiency | congenital mitral valve incompetence | congenital mitral valve insufficiency [FB86.11] Hypertrophy of bone Also known as: Hypertrophy of bone | bone thickening | periosteum thickening | Infantile cortical hyperostoses | Post traumatic subperiosteal ossification === GRAPH WALKS === --- Walk 1 --- [GB61.Z] Chronic kidney disease, stage unspecified --PARENT--> [GB61] Chronic kidney disease Def: Glomerular Filtration Rate (GFR) < 60 ml/min/1.73m² or presence of kidney damage that is present for more than 3 months. Evidence of kidney damage can include structural abnormalities (imaging or hist... --PARENT--> [?] Kidney failure Def: Inability of the kidneys to adequately filter the blood of waste products, with a lower than normal glomerular filtration rate (GFR). Can be abrupt and potentially reversible (acute kidney injury) or ... --- Walk 2 --- [GB61.Z] Chronic kidney disease, stage unspecified --PARENT--> [GB61] Chronic kidney disease Def: Glomerular Filtration Rate (GFR) < 60 ml/min/1.73m² or presence of kidney damage that is present for more than 3 months. Evidence of kidney damage can include structural abnormalities (imaging or hist... --CHILD--> [GB61.0] Chronic kidney disease, stage 1 Def: Kidney damage with normal or increased GFR (>90 ml/min/1.73m²)... --- Walk 3 --- [BC00] Multiple valve disease --PARENT--> [?] Heart valve diseases --CHILD--> [?] Aortic valve disease --- Walk 4 --- [BC00] Multiple valve disease --PARENT--> [?] Heart valve diseases --PARENT--> [11] Diseases of the circulatory system Def: This refers to diseases of the organ system that passes nutrients (such as amino acids, electrolytes and lymph), gases, hormones, blood cells, etc. to and from cells in the body to help fight diseases... --- Walk 5 --- [BB9Z] Pulmonary valve disease, unspecified --PARENT--> [?] Pulmonary valve disease --CHILD--> [BB92] Pulmonary valve stenosis with insufficiency Def: This is a clinical condition in which pulmonary valve stenosis and pulmonary insufficiency are seen together.... --- Walk 6 --- [BB9Z] Pulmonary valve disease, unspecified --PARENT--> [?] Pulmonary valve disease --EXCLUDES--> [?] Congenital anomaly of pulmonary valve Def: A congenital malformation of the heart where the pulmonary valve is abnormal....
[ "[GB61.Z] Chronic kidney disease, stage unspecified\n --PARENT--> [GB61] Chronic kidney disease\n Def: Glomerular Filtration Rate (GFR) < 60 ml/min/1.73m² or presence of kidney damage that is present for more than 3 months. Evidence of kidney damage can include structural abnormalities (imaging or hist...\n --PARENT--> [?] Kidney failure\n Def: Inability of the kidneys to adequately filter the blood of waste products, with a lower than normal glomerular filtration rate (GFR). Can be abrupt and potentially reversible (acute kidney injury) or ...", "[GB61.Z] Chronic kidney disease, stage unspecified\n --PARENT--> [GB61] Chronic kidney disease\n Def: Glomerular Filtration Rate (GFR) < 60 ml/min/1.73m² or presence of kidney damage that is present for more than 3 months. Evidence of kidney damage can include structural abnormalities (imaging or hist...\n --CHILD--> [GB61.0] Chronic kidney disease, stage 1\n Def: Kidney damage with normal or increased GFR (>90 ml/min/1.73m²)...", "[BC00] Multiple valve disease\n --PARENT--> [?] Heart valve diseases\n --CHILD--> [?] Aortic valve disease", "[BC00] Multiple valve disease\n --PARENT--> [?] Heart valve diseases\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...", "[BB9Z] Pulmonary valve disease, unspecified\n --PARENT--> [?] Pulmonary valve disease\n --CHILD--> [BB92] Pulmonary valve stenosis with insufficiency\n Def: This is a clinical condition in which pulmonary valve stenosis and pulmonary insufficiency are seen together....", "[BB9Z] Pulmonary valve disease, unspecified\n --PARENT--> [?] Pulmonary valve disease\n --EXCLUDES--> [?] Congenital anomaly of pulmonary valve\n Def: A congenital malformation of the heart where the pulmonary valve is abnormal...." ]
GB61.Z
Chronic kidney disease, stage unspecified
[ { "from_icd11": "GB61.Z", "icd10_code": "N183", "icd10_title": "Chronic kidney disease, stage 3 (moderate)" }, { "from_icd11": "GB61.Z", "icd10_code": "N189", "icd10_title": "Chronic kidney disease, unspecified" }, { "from_icd11": "GB61.Z", "icd10_code": "N250", "icd10_title": "Renal osteodystrophy" }, { "from_icd11": "GB61.Z", "icd10_code": "N18", "icd10_title": "Chronic kidney disease (CKD)" }, { "from_icd11": "BC00", "icd10_code": "I081", "icd10_title": "Rheumatic disorders of both mitral and tricuspid valves" }, { "from_icd11": "BC00", "icd10_code": "I080", "icd10_title": "Rheumatic disorders of both mitral and aortic valves" }, { "from_icd11": "BC00", "icd10_code": "I082", "icd10_title": "Rheumatic disorders of both aortic and tricuspid valves" }, { "from_icd11": "BC00", "icd10_code": "I083", "icd10_title": "Combined rheumatic disorders of mitral, aortic and tricuspid valves" }, { "from_icd11": "BC00", "icd10_code": "I088", "icd10_title": "Other rheumatic multiple valve diseases" }, { "from_icd11": "BC00", "icd10_code": "I089", "icd10_title": "Rheumatic multiple valve disease, unspecified" }, { "from_icd11": "BC00", "icd10_code": "I05-I09", "icd10_title": "" }, { "from_icd11": "BC00", "icd10_code": "I08", "icd10_title": "Multiple valve diseases" }, { "from_icd11": "BC00", "icd10_code": "I34", "icd10_title": "Nonrheumatic mitral valve disorders" }, { "from_icd11": "BC00", "icd10_code": "I35", "icd10_title": "Nonrheumatic aortic valve disorders" }, { "from_icd11": "BC00", "icd10_code": "I36", "icd10_title": "Nonrheumatic tricuspid valve disorders" } ]
N183
Chronic kidney disease, stage 3 (moderate)
Pathogenic variants in the WDR81 gene located on chromosome 17p13.3 are associated with cerebellar ataxia, impaired intellectual development, and disequilibrium syndrome-2 (CAMRQ2). This disorder is characterized by congenital cerebellar ataxia, intellectual disability, and gait abnormalities . This disorder is extremely rare, with fewer than 20 previously published cases in the literature . All cases of CAMRQ2 that have been reported are consanguineous with autosomal recessive inheritance . The WDR81 gene has been found to show some similarity with genes including NSMAF (neutral sphingomyelinase activation associated factor), NBEA (neurobeachin), and LYST (lysosomal trafficking regulator) . Previously published cases describe other varying features, including thoracic kyphosis and scoliosis, short stature, absent or limited speech, intention tremor, coarse facial features, hirsutism, strabismus, wide and short neck, and small hands and feet . Findings on brain MRI of previously published cases include cerebellar atrophy, generalized brain atrophy, and hypoplasia of the corpus callosum . All previously published cases have occurred in consanguineous families, and the majority of affected individuals ambulated with a quadrupedal gait . Here, we describe a case report of a more mildly affected female with bipedal gait from a nonconsanguineous family, expanding the phenotype of this rare disorder.
4.390625
0.730957
sec[0]/p[0]
en
0.999998
40013199
https://doi.org/10.7759/cureus.78066
[ "cases", "previously", "published", "cerebellar", "this", "gait", "gene", "associated", "ataxia", "intellectual" ]
[ { "code": "JB20.Z", "title": "Single spontaneous delivery, unspecified" }, { "code": "QA48.0", "title": "Care or examination immediately after delivery" }, { "code": "6A02.5", "title": "Autism spectrum disorder with disorder of intellectual development and with absence of functional language" }, { "code": "6A02.3", "title": "Autism spectrum disorder with disorder of intellectual development and with impaired functional language" }, { "code": "6A02.Y", "title": "Other specified autism spectrum disorder" }, { "code": "6A02.2", "title": "Autism spectrum disorder without disorder of intellectual development and with impaired functional language" }, { "code": "6A02.1", "title": "Autism spectrum disorder with disorder of intellectual development and with mild or no impairment of functional language" }, { "code": "LA06.Z", "title": "Cerebellar structural developmental anomalies, unspecified" }, { "code": "8E7Y", "title": "Other specified diseases of the nervous system" }, { "code": "NA07.3Y&XA1CW2", "title": "Laceration of cerebellum" } ]
=== 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 [6A02.5] Autism spectrum disorder with disorder of intellectual development and with absence of functional language Definition: All definitional requirements for both autism spectrum disorder and disorder of intellectual development are met and there is complete, or almost complete, absence of ability relative to the individual’s age to use functional language (spoken or signed) for instrumental purposes, such as to express personal needs and desires Also known as: Autism spectrum disorder with disorder of intellectual development and with absence of functional language | Autism spectrum disorder with disorder of intellectual development and absence of functional language with loss of previously acquired skills | Autism spectrum disorder with disorder of intellectual development and absence of functional language without loss of previously acquired skills [6A02.3] Autism spectrum disorder with disorder of intellectual development and with impaired functional language Definition: All definitional requirements for both autism spectrum disorder and disorder of intellectual development are met and there is marked impairment in functional language (spoken or signed) relative to the individual’s age, with the individual not able to use more than single words or simple phrases for instrumental purposes, such as to express personal needs and desires. Also known as: Autism spectrum disorder with disorder of intellectual development and with impaired functional language | Autism spectrum disorder with disorder of intellectual development and with impaired functional language with loss of previously acquired skills | Childhood disintegrative disorder | Heller syndrome | Disintegrative psychosis [6A02.Y] Other specified autism spectrum disorder Also known as: Other specified autism spectrum disorder | Autism spectrum disorder without disorder of intellectual development and with absence of functional language | Autism spectrum disorder without disorder of intellectual development and with absence of functional language with loss of previously acquired skills | Autism spectrum disorder without disorder of intellectual development and with absence of functional language without loss of previously acquired skills | Atypical autism [6A02.2] Autism spectrum disorder without disorder of intellectual development and with impaired functional language Definition: All definitional requirements for autism spectrum disorder are met, intellectual functioning and adaptive behaviour are found to be at least within the average range (approximately greater than the 2.3rd percentile), and there is marked impairment in functional language (spoken or signed) relative to the individual’s age, with the individual not able to use more than single words or simple phrases for instrumental purposes, such as to express personal needs and desires. Also known as: Autism spectrum disorder without disorder of intellectual development and with impaired functional language | Autism spectrum disorder without disorder of intellectual development and with impaired functional language with loss of previously acquired skills | Autism spectrum disorder without disorder of intellectual development and with impaired functional language without loss of previously acquired skills [6A02.1] Autism spectrum disorder with disorder of intellectual development and with mild or no impairment of functional language Definition: All definitional requirements for both autism spectrum disorder and disorder of intellectual development are met and there is only mild or no impairment in the individual's capacity to use functional language (spoken or signed) for instrumental purposes, such as to express personal needs and desires. Also known as: Autism spectrum disorder with disorder of intellectual development and with mild or no impairment of functional language | Autism spectrum disorder with disorder of intellectual development and without impairment of functional language | Autism spectrum disorder with disorder of intellectual development and with mild or no impairment of functional language with loss of previously acquired skills | Autism spectrum disorder with disorder of intellectual development and with mild or no impairment of functional language without loss of previously acquired skills [LA06.Z] Cerebellar structural developmental anomalies, unspecified Also known as: Cerebellar structural developmental anomalies, unspecified | Cerebellar structural developmental anomalies | Malformations of cerebellum [8E7Y] Other specified diseases of the nervous system Also known as: Other specified diseases of the nervous system | Circumscribed brain atrophy | circumscribed cerebral atrophy | atrophic lobar sclerosis | atrophic lobar brain sclerosis === GRAPH WALKS === --- Walk 1 --- [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--> [QA48.0] Care or examination immediately after delivery --- 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... --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 5 --- [6A02.5] Autism spectrum disorder with disorder of intellectual development and with absence of functional language Def: All definitional requirements for both autism spectrum disorder and disorder of intellectual development are met and there is complete, or almost complete, absence of ability relative to the individua... --PARENT--> [6A02] Autism spectrum disorder Def: Autism spectrum disorder is characterised by persistent deficits in the ability to initiate and to sustain reciprocal social interaction and social communication, and by a range of restricted, repetit... --EXCLUDES--> [?] Rett syndrome Def: A condition in which apparently normal early development is followed by partial or complete loss of speech and of skills in locomotion and use of hands, together with deceleration in head growth, usua... --- Walk 6 --- [6A02.5] Autism spectrum disorder with disorder of intellectual development and with absence of functional language Def: All definitional requirements for both autism spectrum disorder and disorder of intellectual development are met and there is complete, or almost complete, absence of ability relative to the individua... --PARENT--> [6A02] Autism spectrum disorder Def: Autism spectrum disorder is characterised by persistent deficits in the ability to initiate and to sustain reciprocal social interaction and social communication, and by a range of restricted, repetit... --CHILD--> [6A02.0] Autism spectrum disorder without disorder of intellectual development and with mild or no impairment of functional language Def: All definitional requirements for autism spectrum disorder are met, intellectual functioning and adaptive behaviour are found to be at least within the average range (approximately greater than the 2....
[ "[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--> [QA48.0] Care or examination immediately after delivery", "[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...", "[6A02.5] Autism spectrum disorder with disorder of intellectual development and with absence of functional language\n Def: All definitional requirements for both autism spectrum disorder and disorder of intellectual development are met and there is complete, or almost complete, absence of ability relative to the individua...\n --PARENT--> [6A02] Autism spectrum disorder\n Def: Autism spectrum disorder is characterised by persistent deficits in the ability to initiate and to sustain reciprocal social interaction and social communication, and by a range of restricted, repetit...\n --EXCLUDES--> [?] Rett syndrome\n Def: A condition in which apparently normal early development is followed by partial or complete loss of speech and of skills in locomotion and use of hands, together with deceleration in head growth, usua...", "[6A02.5] Autism spectrum disorder with disorder of intellectual development and with absence of functional language\n Def: All definitional requirements for both autism spectrum disorder and disorder of intellectual development are met and there is complete, or almost complete, absence of ability relative to the individua...\n --PARENT--> [6A02] Autism spectrum disorder\n Def: Autism spectrum disorder is characterised by persistent deficits in the ability to initiate and to sustain reciprocal social interaction and social communication, and by a range of restricted, repetit...\n --CHILD--> [6A02.0] Autism spectrum disorder without disorder of intellectual development and with mild or no impairment of functional language\n Def: All definitional requirements for autism spectrum disorder are met, intellectual functioning and adaptive behaviour are found to be at least within the average range (approximately greater than the 2...." ]
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" } ]
O80
Encounter for full-term uncomplicated delivery
A 59-year-old female was seen for recurrent allergic reactions. Her history included anxiety, carpal tunnel syndrome, type 2 diabetes mellitus with diabetic polyneuropathy, essential hypertension, morbid obesity, and opioid use disorder. Her reactions began with palmar and plantar itch, followed by a cascade of variable symptoms, namely, hand edema, generalized urticaria, facial and tongue swelling, palpitations, a lightheaded sensation and presyncope, nausea, vomiting, and diarrhea. These symptoms resolved after about 1 hour and were followed by a day of generalized fatigue. Diphenhydramine had afforded modest relief of her acute symptoms. She reported 8 to 9 episodes during the prior year. The findings of her baseline physical examination were normal, as were her levels of serum tryptase and urinary excretion of MC mediator metabolites ( Table II ). Administration of cetirizine, 10 mg orally per day, was started, and she was instructed to take prednisone, 40 mg, as well as diphenhydramine and famotidine, at the next onset of symptoms. Table II Patient 2 baseline and acute serum tryptase and urinary mast cell mediator metabolite values Mediator (reference range) Baseline value Acute value Acute/baseline Tryptase (ng/mL), (<11.5) 8.6 29.9 3.5 N-MH (μg/g of Cr), (30-200) 76 86 1.1 (2,3-dinor)-11β-PGF 2α pg/mg of Cr, (<1,802) 948 15,246 16.1 LTE 4 (pg/mg of Cr), (≤104) 81 534 6.6 Cr , Creatinine.
4.035156
0.96875
sec[1]/sec[1]/sec[1]/p[0]
en
0.999997
39906893
https://doi.org/10.1016/j.jacig.2024.100399
[ "baseline", "tryptase", "mediator", "reactions", "diphenhydramine", "serum", "urinary", "recurrent", "allergic", "included" ]
[ { "code": "4A85.00", "title": "Drug-induced liver hypersensitivity disease" }, { "code": "8C60.Y", "title": "Other specified myasthenia gravis" }, { "code": "LA8Y", "title": "Other specified structural developmental anomaly of heart or great vessels" }, { "code": "8D88.2", "title": "Immune mediated autonomic neuropathy" }, { "code": "EB02.Y", "title": "Other conditions mediated by cholinergic activation" }, { "code": "NE60", "title": "Harmful effects of drugs, medicaments or biological substances, not elsewhere classified" }, { "code": "6B43", "title": "Adjustment disorder" }, { "code": "NE80.Z", "title": "Injury or harm arising following infusion, transfusion or therapeutic injection, not elsewhere classified, unspecified" }, { "code": "4B24.Z", "title": "Graft-versus-host disease, unspecified" }, { "code": "NE80.3", "title": "Other serum reactions" } ]
=== ICD-11 CODES FOUND === [4A85.00] Drug-induced liver hypersensitivity disease Definition: Drug-induced liver hypersensitivity disease is a relatively rare condition, but can have serious consequences for the individual patient, public health, regulatory agencies and the pharmaceutical industry. It is characterised by elevation in serum alanine-aminotransferase (ALT), conjugated bilirubin, or combined bilirubin, ALT and alkaline phosphatase (AP) levels > 2 times the upper limit of normal (ULN) and the most frequent related drugs are halothane, tienilic acid, dihydralazine, diclofenac, Also known as: Drug-induced liver hypersensitivity disease | medicament-induced liver hypersensitivity disease | Immune-mediated DILI - [drug-induced liver injury] [8C60.Y] Other specified myasthenia gravis Also known as: Other specified myasthenia gravis | Myasthenia gravis, AChR antibody positive | Myasthenia gravis, MuSK antibody positive | Myasthenia gravis, other antibodies positive | Myasthenia gravis, seronegative [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 [8D88.2] Immune mediated autonomic neuropathy Also known as: Immune mediated autonomic neuropathy | Autonomic neuropathy due to Guillain-Barre Syndrome | Postinfectious autonomic neuropathy | Autonomic neuropathy due to certain specified autoimmune diseases | Autoimmune ganglionopathy [EB02.Y] Other conditions mediated by cholinergic activation Also known as: Other conditions mediated by cholinergic activation | Cholinergic pruritus | Cholinergic erythema Includes: Cholinergic pruritus | Cholinergic erythema [NE60] Harmful effects of drugs, medicaments or biological substances, not elsewhere classified Also known as: Harmful effects of drugs, medicaments or biological substances, not elsewhere classified | drugs, medicaments or biological substances, toxicity not elsewhere classified | adverse drug effects | drug reaction NOS | drug allergy NOS Excludes: Alcohol intoxication | pathological drug intoxication | hypersensitivity reaction to correctly administered drug [6B43] Adjustment disorder Definition: Adjustment disorder is a maladaptive reaction to an identifiable psychosocial stressor or multiple stressors (e.g. divorce, illness or disability, socio-economic problems, conflicts at home or work) that usually emerges within a month of the stressor. The disorder is characterised by preoccupation with the stressor or its consequences, including excessive worry, recurrent and distressing thoughts about the stressor, or constant rumination about its implications, as well as by failure to adapt to Also known as: Adjustment disorder | brief situational non-psychotic disorder | adaptation reaction NOS | adjustment reaction | emotional crisis Excludes: separation anxiety disorder of childhood | Recurrent depressive disorder | Single episode depressive disorder [NE80.Z] Injury or harm arising following infusion, transfusion or therapeutic injection, not elsewhere classified, unspecified Also known as: Injury or harm arising following infusion, transfusion or therapeutic injection, not elsewhere classified, unspecified | Injury or harm arising following infusion, transfusion or therapeutic injection, not elsewhere classified | transfusion reaction NOS | Blood transfusion reaction not elsewhere classified | blood transfusion reaction NOS [4B24.Z] Graft-versus-host disease, unspecified Also known as: Graft-versus-host disease, unspecified | Graft-versus-host disease | GVHD - [graft-versus-host disease] | graft-versus-host reaction or disease | GVH - [graft-versus-host] disease [NE80.3] Other serum reactions Also known as: Other serum reactions | Allergic reaction to serum | serum allergy | Complications of vaccination, protein sickness | Protein sickness Excludes: serum hepatitis === GRAPH WALKS === --- Walk 1 --- [4A85.00] Drug-induced liver hypersensitivity disease Def: Drug-induced liver hypersensitivity disease is a relatively rare condition, but can have serious consequences for the individual patient, public health, regulatory agencies and the pharmaceutical indu... --PARENT--> [4A85.0] Drug or pharmacological agents hypersensitivity Def: Drug hypersensitivity reactions are the adverse effects of pharmaceutical formulations (including active drugs and excipients) that clinically resemble allergy. It belongs to type B adverse drug react... --RELATED_TO--> [?] Drug eruptions --- Walk 2 --- [4A85.00] Drug-induced liver hypersensitivity disease Def: Drug-induced liver hypersensitivity disease is a relatively rare condition, but can have serious consequences for the individual patient, public health, regulatory agencies and the pharmaceutical indu... --PARENT--> [4A85.0] Drug or pharmacological agents hypersensitivity Def: Drug hypersensitivity reactions are the adverse effects of pharmaceutical formulations (including active drugs and excipients) that clinically resemble allergy. It belongs to type B adverse drug react... --RELATED_TO--> [?] Drug-induced aplastic anaemia Def: A disease caused by drug intake. This disease is characterised by inability of stem cells to generate new mature cells leading to low levels of red blood cells, white blood cells, platelets. This dise... --- Walk 3 --- [8C60.Y] Other specified myasthenia gravis --PARENT--> [8C60] Myasthenia gravis Def: Myasthenia gravis is the most common acquired auto-antibody mediated neuromuscular transmission disorder. Prevalence is 1–2 per 10,000 persons. Fluctuating weakness increasing with repeated activity a... --PARENT--> [?] Myasthenia gravis or certain specified neuromuscular junction disorders Def: Myasthenia gravis is the most common autoimmune disease affecting the neuromuscular junction and is characterised by painless fatigable muscle weakness. It is caused by autoantibodies against neuromus... --- Walk 4 --- [8C60.Y] Other specified myasthenia gravis --PARENT--> [8C60] Myasthenia gravis Def: Myasthenia gravis is the most common acquired auto-antibody mediated neuromuscular transmission disorder. Prevalence is 1–2 per 10,000 persons. Fluctuating weakness increasing with repeated activity a... --PARENT--> [?] Myasthenia gravis or certain specified neuromuscular junction disorders Def: Myasthenia gravis is the most common autoimmune disease affecting the neuromuscular junction and is characterised by painless fatigable muscle weakness. It is caused by autoantibodies against neuromus... --- Walk 5 --- [LA8Y] Other specified structural developmental anomaly of heart or great vessels --PARENT--> [?] Structural developmental anomaly of heart or great vessels Def: A congenital malformation of the heart and/or great vessels or an acquired abnormality unique to the congenitally malformed heart.... --RELATED_TO--> [?] Congenital cardiac tumor, not otherwise specified Def: A congenital malformation consisting of growth of abnormal tissue within the heart.... --- Walk 6 --- [LA8Y] Other specified structural developmental anomaly of heart or great vessels --PARENT--> [?] Structural developmental anomaly of heart or great vessels Def: A congenital malformation of the heart and/or great vessels or an acquired abnormality unique to the congenitally malformed heart.... --RELATED_TO--> [?] Congenital great vessel related acquired abnormality Def: Any postnatal pathological change in form or function of the heart and/or great vessels consequent to the presence of congenital cardiovascular disease....
[ "[4A85.00] Drug-induced liver hypersensitivity disease\n Def: Drug-induced liver hypersensitivity disease is a relatively rare condition, but can have serious consequences for the individual patient, public health, regulatory agencies and the pharmaceutical indu...\n --PARENT--> [4A85.0] Drug or pharmacological agents hypersensitivity\n Def: Drug hypersensitivity reactions are the adverse effects of pharmaceutical formulations (including active drugs and excipients) that clinically resemble allergy. It belongs to type B adverse drug react...\n --RELATED_TO--> [?] Drug eruptions", "[4A85.00] Drug-induced liver hypersensitivity disease\n Def: Drug-induced liver hypersensitivity disease is a relatively rare condition, but can have serious consequences for the individual patient, public health, regulatory agencies and the pharmaceutical indu...\n --PARENT--> [4A85.0] Drug or pharmacological agents hypersensitivity\n Def: Drug hypersensitivity reactions are the adverse effects of pharmaceutical formulations (including active drugs and excipients) that clinically resemble allergy. It belongs to type B adverse drug react...\n --RELATED_TO--> [?] Drug-induced aplastic anaemia\n Def: A disease caused by drug intake. This disease is characterised by inability of stem cells to generate new mature cells leading to low levels of red blood cells, white blood cells, platelets. This dise...", "[8C60.Y] Other specified myasthenia gravis\n --PARENT--> [8C60] Myasthenia gravis\n Def: Myasthenia gravis is the most common acquired auto-antibody mediated neuromuscular transmission disorder. Prevalence is 1–2 per 10,000 persons. Fluctuating weakness increasing with repeated activity a...\n --PARENT--> [?] Myasthenia gravis or certain specified neuromuscular junction disorders\n Def: Myasthenia gravis is the most common autoimmune disease affecting the neuromuscular junction and is characterised by painless fatigable muscle weakness. It is caused by autoantibodies against neuromus...", "[8C60.Y] Other specified myasthenia gravis\n --PARENT--> [8C60] Myasthenia gravis\n Def: Myasthenia gravis is the most common acquired auto-antibody mediated neuromuscular transmission disorder. Prevalence is 1–2 per 10,000 persons. Fluctuating weakness increasing with repeated activity a...\n --PARENT--> [?] Myasthenia gravis or certain specified neuromuscular junction disorders\n Def: Myasthenia gravis is the most common autoimmune disease affecting the neuromuscular junction and is characterised by painless fatigable muscle weakness. It is caused by autoantibodies against neuromus...", "[LA8Y] Other specified structural developmental anomaly of heart or great vessels\n --PARENT--> [?] Structural developmental anomaly of heart or great vessels\n Def: A congenital malformation of the heart and/or great vessels or an acquired abnormality unique to the congenitally malformed heart....\n --RELATED_TO--> [?] Congenital cardiac tumor, not otherwise specified\n Def: A congenital malformation consisting of growth of abnormal tissue within the heart....", "[LA8Y] Other specified structural developmental anomaly of heart or great vessels\n --PARENT--> [?] Structural developmental anomaly of heart or great vessels\n Def: A congenital malformation of the heart and/or great vessels or an acquired abnormality unique to the congenitally malformed heart....\n --RELATED_TO--> [?] Congenital great vessel related acquired abnormality\n Def: Any postnatal pathological change in form or function of the heart and/or great vessels consequent to the presence of congenital cardiovascular disease...." ]
4A85.00
Drug-induced liver hypersensitivity disease
[ { "from_icd11": "4A85.00", "icd10_code": "K71", "icd10_title": "Toxic liver disease" }, { "from_icd11": "LA8Y", "icd10_code": "Q248 ", "icd10_title": "" }, { "from_icd11": "8D88.2", "icd10_code": "G991", "icd10_title": "" }, { "from_icd11": "NE60", "icd10_code": "T50A95A", "icd10_title": "Adverse effect of other bacterial vaccines, initial encounter" }, { "from_icd11": "NE60", "icd10_code": "T50Z15A", "icd10_title": "Adverse effect of immunoglobulin, initial encounter" }, { "from_icd11": "NE60", "icd10_code": "T50Z95A", "icd10_title": "Adverse effect of other vaccines and biological substances, initial encounter" }, { "from_icd11": "NE60", "icd10_code": "T50A95S", "icd10_title": "Adverse effect of other bacterial vaccines, sequela" }, { "from_icd11": "NE60", "icd10_code": "T50B95A", "icd10_title": "Adverse effect of other viral vaccines, initial encounter" }, { "from_icd11": "NE60", "icd10_code": "T50A25A", "icd10_title": "Adverse effect of mixed bacterial vaccines without a pertussis component, initial encounter" }, { "from_icd11": "NE60", "icd10_code": "T50A91A", "icd10_title": "Poisoning by other bacterial vaccines, accidental (unintentional), initial encounter" }, { "from_icd11": "NE60", "icd10_code": "T498X5A", "icd10_title": "Adverse effect of other topical agents, initial encounter" }, { "from_icd11": "NE60", "icd10_code": "T48905A", "icd10_title": "Adverse effect of unspecified agents primarily acting on the respiratory system, initial encounter" }, { "from_icd11": "NE60", "icd10_code": "T48995A", "icd10_title": "Adverse effect of other agents primarily acting on the respiratory system, initial encounter" }, { "from_icd11": "NE60", "icd10_code": "T50A15A", "icd10_title": "Adverse effect of pertussis vaccine, including combinations with a pertussis component, initial encounter" }, { "from_icd11": "NE60", "icd10_code": "T50B15A", "icd10_title": "Adverse effect of smallpox vaccines, initial encounter" } ]
K71
Toxic liver disease
During his hospital stay, pulmonary consolidation involving the right upper lobe, with pleural effusion and enlarged mediastinal lymph nodes, was detected, associated with an increase in inflammatory markers. Suspecting an infectious origin, systemic empirical antibiotic therapy (levofloxacin, later switched to piperacillin/tazobactam) was administered. A few days later, the patient developed disseminated hemorrhagic edematous cutaneous lesions with vesiculation and necrotic trend toward punched-out ulcerations, primarily on the head and, to a lesser extent, the trunk and limbs, where they appeared more scattered and with an umbilicated morphology. Two days after the onset of cutaneous manifestations, the patient was transferred to the intensive care unit (ICU) due to a deteriorating general condition, with respiratory failure and fever requiring invasive ventilation. The cutaneous manifestations worsened, with extensive skin necrosis, particularly in the nasal area, covered by granulation tissue and hemorrhagic and bullous lesions . Erosive lesions involved the tongue, oral, and nasal mucosa with significant crusting of the lips. A biopsy was taken from the right arm for histological examination, cultures, and direct immunofluorescence (DIF). Systemic therapy with antifungal and antiviral agents was initiated, and antibiotic therapy was continued. However, the patient continued to deteriorate.
3.931641
0.979004
sec[1]/p[1]
en
0.999997
39444817
https://doi.org/10.3389/fmed.2024.1468712
[ "cutaneous", "lesions", "systemic", "antibiotic", "hemorrhagic", "manifestations", "nasal", "stay", "pulmonary", "consolidation" ]
[ { "code": "ME60.Z", "title": "Skin lesion of unspecified nature" }, { "code": "EB90.40", "title": "Dystrophic calcification of the skin of uncertain or unspecified aetiology" }, { "code": "ND56.0", "title": "Superficial injury of unspecified body region" }, { "code": "ME60.3", "title": "Keratosis of skin of uncertain or unspecified nature" }, { "code": "EB90.1", "title": "Cutaneous mucinosis" }, { "code": "FA5Z", "title": "Arthropathies, unspecified" }, { "code": "FC0Z", "title": "Diseases of the musculoskeletal system or connective tissue, unspecified" }, { "code": "MD41", "title": "Clinical findings on diagnostic imaging of lung" }, { "code": "GC2Z&XA6KU8", "title": "Disease of kidney, not elsewhere classified" }, { "code": "4A42.Z", "title": "Systemic sclerosis, unspecified" } ]
=== ICD-11 CODES FOUND === [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 [EB90.40] Dystrophic calcification of the skin of uncertain or unspecified aetiology Definition: Abnormal deposition of calcium in the skin and subcutaneous tissues of unknown (idiopathic) or unspecified cause. Also known as: Dystrophic calcification of the skin of uncertain or unspecified aetiology | Calcinosis cutis of uncertain or unspecified aetiology | Osteoma cutis | Cutaneous ossification | Subepidermal calcified nodule Includes: Calcinosis cutis [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 [ME60.3] Keratosis of skin of uncertain or unspecified nature Also known as: Keratosis of skin of uncertain or unspecified nature | Keratosis of skin | Cutaneous horn | Keratin horn | Cornu cutaneum [EB90.1] Cutaneous mucinosis Definition: Skin disorders characterised by accumulation of mucin in the skin Also known as: Cutaneous mucinosis | Mucinosis of skin [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 [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 [4A42.Z] Systemic sclerosis, unspecified Also known as: Systemic sclerosis, unspecified | Systemic sclerosis | Systemic scleroderma | progressive scleroderma | Acroscleriasis === GRAPH WALKS === --- Walk 1 --- [ME60.Z] Skin lesion of unspecified nature --PARENT--> [ME60] Skin lesion of uncertain or unspecified nature Def: To be used where there is either significant uncertainty or alternatively no information as to the nature of a circumscribed skin lesion. This is of particular importance with regard to whether or not... --CHILD--> [ME60.2] Ulcer of skin of uncertain nature Def: This denotes the presence of a skin ulcer but uncertainty as to its nature. No inference as to whether the ulcer might be of serious significance (e.g. suspected skin cancer) is made.... --- Walk 2 --- [ME60.Z] Skin lesion of unspecified nature --PARENT--> [ME60] Skin lesion of uncertain or unspecified nature Def: To be used where there is either significant uncertainty or alternatively no information as to the nature of a circumscribed skin lesion. This is of particular importance with regard to whether or not... --CHILD--> [ME60.2] Ulcer of skin of uncertain nature Def: This denotes the presence of a skin ulcer but uncertainty as to its nature. No inference as to whether the ulcer might be of serious significance (e.g. suspected skin cancer) is made.... --- Walk 3 --- [EB90.40] Dystrophic calcification of the skin of uncertain or unspecified aetiology Def: Abnormal deposition of calcium in the skin and subcutaneous tissues of unknown (idiopathic) or unspecified cause.... --RELATED_TO--> [?] Scrotal calcinosis Def: Scrotal calcinosis is an uncommon condition characterised by the appearance in adolescence or early adult life of multiple calcified dermal nodules within scrotal skin. Although some cases may be rela... --PARENT--> [?] Dystrophic calcification of the skin of uncertain or unspecified aetiology Def: Abnormal deposition of calcium in the skin and subcutaneous tissues of unknown (idiopathic) or unspecified cause.... --- Walk 4 --- [EB90.40] Dystrophic calcification of the skin of uncertain or unspecified aetiology Def: Abnormal deposition of calcium in the skin and subcutaneous tissues of unknown (idiopathic) or unspecified cause.... --PARENT--> [EB90.4] Calcification of skin or subcutaneous tissue Def: A heterogeneous group of disorders which result in deposition of calcium in skin and soft tissues.... --CHILD--> [EB90.41] Calcific panniculitis Def: Calcific panniculitis presents as discrete, firm subcutaneous masses, often affecting the thighs and hips. It is strongly associated with hyperparathyroidism, particularly in the context of chronic re... --- Walk 5 --- [ND56.0] Superficial injury of unspecified body region --EXCLUDES--> [?] Superficial injuries involving multiple body regions --CHILD--> [?] Superficial injuries involving thorax with abdomen, lower back or pelvis --- Walk 6 --- [ND56.0] Superficial injury of unspecified body region --RELATED_TO--> [?] Haematoma of surgical wound of skin Def: Collection of blood within skin and soft tissues following surgical wound of skin usually resulting from defective haemostasis... --PARENT--> [?] Surgical wound of skin
[ "[ME60.Z] Skin lesion of unspecified nature\n --PARENT--> [ME60] Skin lesion of uncertain or unspecified nature\n Def: To be used where there is either significant uncertainty or alternatively no information as to the nature of a circumscribed skin lesion. This is of particular importance with regard to whether or not...\n --CHILD--> [ME60.2] Ulcer of skin of uncertain nature\n Def: This denotes the presence of a skin ulcer but uncertainty as to its nature. No inference as to whether the ulcer might be of serious significance (e.g. suspected skin cancer) is made....", "[ME60.Z] Skin lesion of unspecified nature\n --PARENT--> [ME60] Skin lesion of uncertain or unspecified nature\n Def: To be used where there is either significant uncertainty or alternatively no information as to the nature of a circumscribed skin lesion. This is of particular importance with regard to whether or not...\n --CHILD--> [ME60.2] Ulcer of skin of uncertain nature\n Def: This denotes the presence of a skin ulcer but uncertainty as to its nature. No inference as to whether the ulcer might be of serious significance (e.g. suspected skin cancer) is made....", "[EB90.40] Dystrophic calcification of the skin of uncertain or unspecified aetiology\n Def: Abnormal deposition of calcium in the skin and subcutaneous tissues of unknown (idiopathic) or unspecified cause....\n --RELATED_TO--> [?] Scrotal calcinosis\n Def: Scrotal calcinosis is an uncommon condition characterised by the appearance in adolescence or early adult life of multiple calcified dermal nodules within scrotal skin. Although some cases may be rela...\n --PARENT--> [?] Dystrophic calcification of the skin of uncertain or unspecified aetiology\n Def: Abnormal deposition of calcium in the skin and subcutaneous tissues of unknown (idiopathic) or unspecified cause....", "[EB90.40] Dystrophic calcification of the skin of uncertain or unspecified aetiology\n Def: Abnormal deposition of calcium in the skin and subcutaneous tissues of unknown (idiopathic) or unspecified cause....\n --PARENT--> [EB90.4] Calcification of skin or subcutaneous tissue\n Def: A heterogeneous group of disorders which result in deposition of calcium in skin and soft tissues....\n --CHILD--> [EB90.41] Calcific panniculitis\n Def: Calcific panniculitis presents as discrete, firm subcutaneous masses, often affecting the thighs and hips. It is strongly associated with hyperparathyroidism, particularly in the context of chronic re...", "[ND56.0] Superficial injury of unspecified body region\n --EXCLUDES--> [?] Superficial injuries involving multiple body regions\n --CHILD--> [?] Superficial injuries involving thorax with abdomen, lower back or pelvis", "[ND56.0] Superficial injury of unspecified body region\n --RELATED_TO--> [?] Haematoma of surgical wound of skin\n Def: Collection of blood within skin and soft tissues following surgical wound of skin usually resulting from defective haemostasis...\n --PARENT--> [?] Surgical wound of skin" ]
ME60.Z
Skin lesion of unspecified nature
[ { "from_icd11": "ME60.Z", "icd10_code": "L989", "icd10_title": "Disorder of the skin and subcutaneous tissue, unspecified" }, { "from_icd11": "EB90.40", "icd10_code": "L943", "icd10_title": "Sclerodactyly" }, { "from_icd11": "EB90.40", "icd10_code": "L949", "icd10_title": "Localized connective tissue disorder, unspecified" }, { "from_icd11": "EB90.40", "icd10_code": "L942", "icd10_title": "Calcinosis cutis" }, { "from_icd11": "EB90.40", "icd10_code": "L94", "icd10_title": "Other localized connective tissue disorders" }, { "from_icd11": "ND56.0", "icd10_code": "T009", "icd10_title": "" }, { "from_icd11": "ND56.0", "icd10_code": "T140", "icd10_title": "" }, { "from_icd11": "ME60.3", "icd10_code": "L570", "icd10_title": "Actinic keratosis" }, { "from_icd11": "EB90.1", "icd10_code": "L985", "icd10_title": "Mucinosis of the skin" }, { "from_icd11": "EB90.1", "icd10_code": "L652", "icd10_title": "Alopecia mucinosa" }, { "from_icd11": "FA5Z", "icd10_code": "M00-M25", "icd10_title": "" }, { "from_icd11": "FC0Z", "icd10_code": "XIII", "icd10_title": "" }, { "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": "4A42.Z", "icd10_code": "M3481", "icd10_title": "Systemic sclerosis with lung involvement" } ]
L989
Disorder of the skin and subcutaneous tissue, unspecified
The 63-year-old female reported herein developed a very rare postoperative complication of chronic pancreatitis after a commonly performed elective lumbar spine surgery for non-scoliosis arthritis. Her chronic pancreatitis thereafter became associated with a large pancreatic pseudocyst, which was ultimately treated successfully with an open Roux-en-Y cystojejunostomy. Although there are several possible etiologies of pancreatitis occurring soon after spinal surgery in adults, we could not identify, with high certainty, the cause of our patient’s postoperative complication. Leukocytosis was detected within a few days of symptom onset; however, this was not considered as being possibly associated with pancreatitis. This was despite her chief complaints of abdominal pain, nausea, vomiting, and general discomfort, as well as high amylase levels found in her retroperitoneal fluid. Because pancreatitis can be an elusive complication of spinal surgery in an adult, healthcare providers should consider this diagnosis prominently in the differential diagnosis for the underlying cause of these early postoperative symptoms and leukocytosis. We report this case not only because of its rarity but also to alert surgeons and other healthcare providers that pancreatitis can occur acutely in the postoperative period in adults and evolve into a chronic problem (pseudocyst formation) requiring surgical correction.
4.074219
0.964844
sec[3]/p[0]
en
0.999996
39463520
https://doi.org/10.7759/cureus.70272
[ "pancreatitis", "postoperative", "this", "complication", "associated", "pseudocyst", "spinal", "adults", "cause", "leukocytosis" ]
[ { "code": "DC31.Z", "title": "Acute pancreatitis, unspecified" }, { "code": "DC32.Z", "title": "Chronic pancreatitis, unspecified" }, { "code": "DC34", "title": "Obstructive pancreatitis" }, { "code": "NB91.4Z", "title": "Injury of pancreas, unspecified" }, { "code": "DC32.0", "title": "Calcific pancreatitis" }, { "code": "NE81.0Z", "title": "Haemorrhage or haematoma of other or unspecified site complicating a procedure, not elsewhere classified" }, { "code": "NE81.3", "title": "Postsurgical leak" }, { "code": "QF00", "title": "Acquired absence of limb" }, { "code": "DB30.2", "title": "Adhesions of large intestine with obstruction" }, { "code": "MG30.21", "title": "Chronic postsurgical pain" } ]
=== ICD-11 CODES FOUND === [DC31.Z] Acute pancreatitis, unspecified Also known as: Acute pancreatitis, unspecified | Acute pancreatitis | pancreatitis NOS | acute pancreas inflammation [DC32.Z] Chronic pancreatitis, unspecified Also known as: Chronic pancreatitis, unspecified | Chronic pancreatitis [DC34] Obstructive pancreatitis Definition: This is obstruction in the inflammation of the pancreas which requires immediate medical attention and hospitalization during an attack that has multiple causes and symptoms, which occurs when pancreatic enzymes (especially trypsin) that digest food are activated in the pancreas instead of the small intestine. Also known as: Obstructive pancreatitis [NB91.4Z] Injury of pancreas, unspecified Also known as: Injury of pancreas, unspecified | Injury of pancreas | pancreatic injury | traumatic pancreatitis [DC32.0] Calcific pancreatitis Definition: This is inflammation of the pancreas which requires immediate medical attention and hospitalization during an attack, which calcium salts build up in soft tissue, causing it to harden. Also known as: Calcific pancreatitis [NE81.0Z] Haemorrhage or haematoma of other or unspecified site complicating a procedure, not elsewhere classified Also known as: Haemorrhage or haematoma of other or unspecified site complicating a procedure, not elsewhere classified | Haemorrhage or haematoma complicating a procedure, not elsewhere classified | postoperative haemorrhage | postoperative bleeding | Haemorrhage at any site resulting from a procedure [NE81.3] Postsurgical leak Also known as: Postsurgical leak | postoperative leak | Postsurgical air leak | postoperative air leak | Postsurgical bile leak Excludes: Malfunction or complication of external stoma of digestive organs | Tracheostomy malfunction [QF00] Acquired absence of limb Also known as: Acquired absence of limb | post traumatic loss of limb | postoperative loss of limb | bilateral amputee | amputee Includes: postoperative loss of limb | post traumatic loss of limb Excludes: Other acquired deformities of limbs | Congenital absence of thigh or lower leg with foot present | Congenital absence of both lower leg and foot [DB30.2] Adhesions of large intestine with obstruction Definition: Large bowel obstruction resulting from intraabdominal adhesion due to laparotomy, trauma, and intraabdominal inflammation such as endometriosis. Also known as: Adhesions of large intestine with obstruction | Postoperative obstruction of the large intestine [MG30.21] Chronic postsurgical pain Definition: Chronic postsurgical pain is chronic pain developing or increasing in intensity after a surgical procedure and persisting beyond the healing process, i.e. at least 3 months after surgery. The pain is either localised to the surgical field, projected to the innervation territory of a nerve situated in this area, or referred to a dermatome (after surgery/injury to deep somatic or visceral tissues). Other causes of pain including infection, malignancy etc. need to be excluded as well as pain contin Also known as: Chronic postsurgical pain | postsurgical pain | chronic postoperative pain | chronic postamputation pain | Chronic pain after spinal surgery Includes: Chronic pain after spinal surgery | Chronic pain after herniotomy | Chronic pain after hysterectomy === GRAPH WALKS === --- Walk 1 --- [DC31.Z] Acute pancreatitis, unspecified --PARENT--> [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... --CHILD--> [DC31.1] Acute alcohol-induced pancreatitis Def: Acute pancreatitis associated with alcohol consumption. Although alcohol consumption is a major cause of this disease, the diagnosis should be made after exclusion of other etiologies.... --- Walk 2 --- [DC31.Z] Acute pancreatitis, unspecified --PARENT--> [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... --CHILD--> [DC31.2] Acute biliary pancreatitis Def: Acute pancreatitis associated with gallstone. Although gallstone is a major etiology, the diagnosis should be made after exclusion of other etiologies. Bile reflux into pancreatic duct caused by an im... --- Walk 3 --- [DC32.Z] Chronic pancreatitis, unspecified --PARENT--> [DC32] Chronic pancreatitis --EXCLUDES--> [?] Cystic fibrosis of pancreas with pancreatic insufficiency Def: This is an autosomal recessive genetic disorder of the pancreas, that is characterised by abnormal transport of chloride and sodium across an epithelium, leading to thick, viscous secretions, with pan... --- Walk 4 --- [DC32.Z] Chronic pancreatitis, unspecified --PARENT--> [DC32] Chronic pancreatitis --CHILD--> [DC32.2] Hereditary chronic pancreatitis Def: Hereditary chronic pancreatitis is a very rare form of childhood onset chronic pancreatitis. With the exception of an earlier onset and a slower progression the clinical course, the morphological feat... --- Walk 5 --- [DC34] Obstructive pancreatitis Def: This is obstruction in the inflammation of the pancreas which requires immediate medical attention and hospitalization during an attack that has multiple causes and symptoms, which occurs when pancrea... --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 6 --- [DC34] Obstructive pancreatitis Def: This is obstruction in the inflammation of the pancreas which requires immediate medical attention and hospitalization during an attack that has multiple causes and symptoms, which occurs when pancrea... --PARENT--> [?] Diseases of pancreas Def: This is a group of conditions characterised as being in or associated with the pancreas.... --CHILD--> [DC30] Cystic diseases of the pancreas Def: This is a closed sac, having a distinct membrane and division compared to the nearby tissue, which may contain air, fluids, or semi-solid material, of the pancreas....
[ "[DC31.Z] Acute pancreatitis, unspecified\n --PARENT--> [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...\n --CHILD--> [DC31.1] Acute alcohol-induced pancreatitis\n Def: Acute pancreatitis associated with alcohol consumption. Although alcohol consumption is a major cause of this disease, the diagnosis should be made after exclusion of other etiologies....", "[DC31.Z] Acute pancreatitis, unspecified\n --PARENT--> [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...\n --CHILD--> [DC31.2] Acute biliary pancreatitis\n Def: Acute pancreatitis associated with gallstone. Although gallstone is a major etiology, the diagnosis should be made after exclusion of other etiologies. Bile reflux into pancreatic duct caused by an im...", "[DC32.Z] Chronic pancreatitis, unspecified\n --PARENT--> [DC32] Chronic pancreatitis\n --EXCLUDES--> [?] Cystic fibrosis of pancreas with pancreatic insufficiency\n Def: This is an autosomal recessive genetic disorder of the pancreas, that is characterised by abnormal transport of chloride and sodium across an epithelium, leading to thick, viscous secretions, with pan...", "[DC32.Z] Chronic pancreatitis, unspecified\n --PARENT--> [DC32] Chronic pancreatitis\n --CHILD--> [DC32.2] Hereditary chronic pancreatitis\n Def: Hereditary chronic pancreatitis is a very rare form of childhood onset chronic pancreatitis. With the exception of an earlier onset and a slower progression the clinical course, the morphological feat...", "[DC34] Obstructive pancreatitis\n Def: This is obstruction in the inflammation of the pancreas which requires immediate medical attention and hospitalization during an attack that has multiple causes and symptoms, which occurs when pancrea...\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", "[DC34] Obstructive pancreatitis\n Def: This is obstruction in the inflammation of the pancreas which requires immediate medical attention and hospitalization during an attack that has multiple causes and symptoms, which occurs when pancrea...\n --PARENT--> [?] Diseases of pancreas\n Def: This is a group of conditions characterised as being in or associated with the pancreas....\n --CHILD--> [DC30] Cystic diseases of the pancreas\n Def: This is a closed sac, having a distinct membrane and division compared to the nearby tissue, which may contain air, fluids, or semi-solid material, of the pancreas...." ]
DC31.Z
Acute pancreatitis, unspecified
[ { "from_icd11": "DC31.Z", "icd10_code": "K8580", "icd10_title": "Other acute pancreatitis without necrosis or infection" }, { "from_icd11": "DC31.Z", "icd10_code": "K8581", "icd10_title": "Other acute pancreatitis with uninfected necrosis" }, { "from_icd11": "DC31.Z", "icd10_code": "K8591", "icd10_title": "Acute pancreatitis with uninfected necrosis, unspecified" }, { "from_icd11": "DC31.Z", "icd10_code": "K8592", "icd10_title": "Acute pancreatitis with infected necrosis, unspecified" }, { "from_icd11": "DC31.Z", "icd10_code": "K8582", "icd10_title": "Other acute pancreatitis with infected necrosis" }, { "from_icd11": "DC31.Z", "icd10_code": "K8590", "icd10_title": "Acute pancreatitis without necrosis or infection, unspecified" }, { "from_icd11": "DC31.Z", "icd10_code": "K859", "icd10_title": "Acute pancreatitis, unspecified" }, { "from_icd11": "DC31.Z", "icd10_code": "K858", "icd10_title": "Other acute pancreatitis" }, { "from_icd11": "DC31.Z", "icd10_code": "K85", "icd10_title": "Acute pancreatitis" }, { "from_icd11": "DC32.Z", "icd10_code": "K861", "icd10_title": "Other chronic pancreatitis" }, { "from_icd11": "DC32.Z", "icd10_code": "K86", "icd10_title": "Other diseases of pancreas" }, { "from_icd11": "DC34", "icd10_code": "K8681", "icd10_title": "Exocrine pancreatic insufficiency" }, { "from_icd11": "DC34", "icd10_code": "K8689", "icd10_title": "Other specified diseases of pancreas" }, { "from_icd11": "DC34", "icd10_code": "K868", "icd10_title": "Other specified diseases of pancreas" }, { "from_icd11": "NB91.4Z", "icd10_code": "S36220A", "icd10_title": "Contusion of head of pancreas, initial encounter" } ]
K8580
Other acute pancreatitis without necrosis or infection
His serum creatine kinase level was significantly elevated at 17705 U/L (normal: 39–192 U/L). Other laboratory results were as follows: troponin I 0.299 ug/L (normal: 0–0.06 ug/L), lactate dehydrogenase 650 U/L (normal: 120–246 U/L), alanine aminotransferase 160 U/L (normal: <49 U/L), aspartate aminotransferase 297 U/L (normal: <49 U/L). Blood cell counts, thyroid function, parathyroid hormone, renal function, bone density, and spinal X-ray yielded no abnormal results. The electrocardiogram showed sinus arrhythmia and rightward deviation of the electrical axis. The echocardiography demonstrated a normal heart function and structure. The magnetic resonance imaging of the thigh muscles of both lower limbs suggested partial fatty infiltration of the gluteus maximus muscle bilaterally , with no significant fatty replacement of his bilateral thigh muscle. Simultaneously, we communicated with the parents of the patient and recommended that the child undergo a comprehensive magnetic resonance imaging of the brain. However, the parents opted to refuse due to financial constraints and the child’s lack of cooperation, which would necessitate the use of sedatives. Therefore, the child’s clinical symptoms, physical examination, magnetic resonance imaging findings of the thigh muscles of both lower limbs, and the markedly increased creatine kinase levels together indicated to us that the boy might have BMD.
3.984375
0.964844
sec[1]/sec[2]/p[0]
en
0.999999
39659883
https://doi.org/10.3389/fnins.2024.1459582
[ "function", "magnetic", "resonance", "imaging", "thigh", "creatine", "kinase", "aminotransferase", "muscles", "both" ]
[ { "code": "DD91.Z", "title": "Irritable bowel syndrome or functional bowel disorders, unspecified" }, { "code": "9E1Z", "title": "Diseases of the visual system, unspecified" }, { "code": "6B60.Z", "title": "Dissociative neurological symptom disorder, with unspecified symptoms" }, { "code": "6B60.8Y", "title": "Dissociative neurological symptom disorder, with other specified movement disturbance" }, { "code": "6B60.3", "title": "Dissociative neurological symptom disorder, with other sensory disturbance" }, { "code": "NA06.80", "title": "Retained intraocular magnetic foreign body, unilateral" }, { "code": "NA06.80&XA03X9", "title": "Retained magnetic foreign body in ciliary body, unilateral" }, { "code": "NA06.80&XA4HU2", "title": "Retained magnetic foreign body in vitreous, unilateral" }, { "code": "NA06.80&XA3GW7", "title": "Retained magnetic foreign body in iris, unilateral" }, { "code": "NA06.80&XA13U9", "title": "Retained magnetic foreign body in lens, unilateral" } ]
=== ICD-11 CODES FOUND === [DD91.Z] Irritable bowel syndrome or functional bowel disorders, unspecified Also known as: Irritable bowel syndrome or functional bowel disorders, unspecified | Irritable bowel syndrome or certain specified functional bowel disorders | Functional intestinal disorders NOS [9E1Z] Diseases of the visual system, unspecified Also known as: Diseases of the visual system, unspecified | eye diseases NOS | disorder of vision | visual disorder [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 [6B60.8Y] Dissociative neurological symptom disorder, with other specified movement disturbance Also known as: Dissociative neurological symptom disorder, with other specified movement disturbance | Functional movement disorder | Other functional hyperkinetic movements [6B60.3] Dissociative neurological symptom disorder, with other sensory disturbance Definition: Dissociative neurological symptom disorder, with other sensory disturbance is characterised by sensory symptoms not identified in other specific categories in this grouping such as numbness, tightness, tingling, burning, pain, or other symptoms related to touch, smell, taste, balance, proprioception, kinesthesia, or thermoception. The symptoms are not consistent with a recognised disease of the nervous system, other mental, behavioural or neurodevelopmental disorder, or other medical condition a Also known as: Dissociative neurological symptom disorder, with other sensory disturbance | Functional neurological symptom disorder, with alteration of sensation | Functional sensory disorder | Functional neurological symptom disorder, with other sensory disturbance [NA06.80] Retained intraocular magnetic foreign body, unilateral Also known as: Retained intraocular magnetic foreign body, unilateral | old intraocular magnetic foreign body | retained magnetic intraocular foreign body | old magnetic foreign body in eyeball | Retained magnetic foreign body in anterior chamber, unilateral Includes: old magnetic foreign body in eyeball === GRAPH WALKS === --- Walk 1 --- [DD91.Z] Irritable bowel syndrome or functional bowel disorders, unspecified --PARENT--> [DD91] Irritable bowel syndrome or certain specified functional bowel disorders Def: This group incorporates functional bowel disorders which principally present symptoms attributable to the intestinal tract in the absence of specific and unique organic pathology in the small and larg... --CHILD--> [DD91.0] Irritable bowel syndrome Def: Irritable bowel syndrome (IBS) is a functional bowel disorder in which abdominal pain or discomfort is associated with defecation or a change in bowel habit, and with features of disordered defecation... --- Walk 2 --- [DD91.Z] Irritable bowel syndrome or functional bowel disorders, unspecified --PARENT--> [DD91] Irritable bowel syndrome or certain specified functional bowel disorders Def: This group incorporates functional bowel disorders which principally present symptoms attributable to the intestinal tract in the absence of specific and unique organic pathology in the small and larg... --CHILD--> [DD91.2] Functional diarrhoea Def: Functional diarrhoea is a continuous or recurrent syndrome characterised by the passage of loose (mushy) or watery stools without abdominal pain or discomfort.... --- Walk 3 --- [9E1Z] Diseases of the visual system, unspecified --PARENT--> [09] Diseases of the visual system Def: This refers to any diseases of the visual system, which includes the eyes and adnexa, the visual pathways and brain areas, which initiate and control visual perception and visually guided behaviour.... --CHILD--> [?] Disorders of the ocular adnexa or orbit --- Walk 4 --- [9E1Z] Diseases of the visual system, unspecified --PARENT--> [09] Diseases of the visual system Def: This refers to any diseases of the visual system, which includes the eyes and adnexa, the visual pathways and brain areas, which initiate and control visual perception and visually guided behaviour.... --CHILD--> [?] Disorders of the ocular adnexa or orbit --- Walk 5 --- [6B60.Z] Dissociative neurological symptom disorder, with unspecified symptoms --PARENT--> [6B60] Dissociative neurological symptom disorder Def: Dissociative neurological symptom disorder is characterised by the presentation of motor, sensory, or cognitive symptoms that imply an involuntary discontinuity in the normal integration of motor, sen... --PARENT--> [?] Dissociative disorders Def: Dissociative disorders are characterised by involuntary disruption or discontinuity in the normal integration of one or more of the following: identity, sensations, perceptions, affects, thoughts, mem... --- Walk 6 --- [6B60.Z] Dissociative neurological symptom disorder, with unspecified symptoms --PARENT--> [6B60] Dissociative neurological symptom disorder Def: Dissociative neurological symptom disorder is characterised by the presentation of motor, sensory, or cognitive symptoms that imply an involuntary discontinuity in the normal integration of motor, sen... --CHILD--> [6B60.0] Dissociative neurological symptom disorder, with visual disturbance Def: Dissociative neurological symptom disorder, with visual disturbance is characterised by visual symptoms such as blindness, tunnel vision, diplopia, visual distortions or hallucinations that are not co...
[ "[DD91.Z] Irritable bowel syndrome or functional bowel disorders, unspecified\n --PARENT--> [DD91] Irritable bowel syndrome or certain specified functional bowel disorders\n Def: This group incorporates functional bowel disorders which principally present symptoms attributable to the intestinal tract in the absence of specific and unique organic pathology in the small and larg...\n --CHILD--> [DD91.0] Irritable bowel syndrome\n Def: Irritable bowel syndrome (IBS) is a functional bowel disorder in which abdominal pain or discomfort is associated with defecation or a change in bowel habit, and with features of disordered defecation...", "[DD91.Z] Irritable bowel syndrome or functional bowel disorders, unspecified\n --PARENT--> [DD91] Irritable bowel syndrome or certain specified functional bowel disorders\n Def: This group incorporates functional bowel disorders which principally present symptoms attributable to the intestinal tract in the absence of specific and unique organic pathology in the small and larg...\n --CHILD--> [DD91.2] Functional diarrhoea\n Def: Functional diarrhoea is a continuous or recurrent syndrome characterised by the passage of loose (mushy) or watery stools without abdominal pain or discomfort....", "[9E1Z] Diseases of the visual system, unspecified\n --PARENT--> [09] Diseases of the visual system\n Def: This refers to any diseases of the visual system, which includes the eyes and adnexa, the visual pathways and brain areas, which initiate and control visual perception and visually guided behaviour....\n --CHILD--> [?] Disorders of the ocular adnexa or orbit", "[9E1Z] Diseases of the visual system, unspecified\n --PARENT--> [09] Diseases of the visual system\n Def: This refers to any diseases of the visual system, which includes the eyes and adnexa, the visual pathways and brain areas, which initiate and control visual perception and visually guided behaviour....\n --CHILD--> [?] Disorders of the ocular adnexa or orbit", "[6B60.Z] Dissociative neurological symptom disorder, with unspecified symptoms\n --PARENT--> [6B60] Dissociative neurological symptom disorder\n Def: Dissociative neurological symptom disorder is characterised by the presentation of motor, sensory, or cognitive symptoms that imply an involuntary discontinuity in the normal integration of motor, sen...\n --PARENT--> [?] Dissociative disorders\n Def: Dissociative disorders are characterised by involuntary disruption or discontinuity in the normal integration of one or more of the following: identity, sensations, perceptions, affects, thoughts, mem...", "[6B60.Z] Dissociative neurological symptom disorder, with unspecified symptoms\n --PARENT--> [6B60] Dissociative neurological symptom disorder\n Def: Dissociative neurological symptom disorder is characterised by the presentation of motor, sensory, or cognitive symptoms that imply an involuntary discontinuity in the normal integration of motor, sen...\n --CHILD--> [6B60.0] Dissociative neurological symptom disorder, with visual disturbance\n Def: Dissociative neurological symptom disorder, with visual disturbance is characterised by visual symptoms such as blindness, tunnel vision, diplopia, visual distortions or hallucinations that are not co..." ]
DD91.Z
Irritable bowel syndrome or functional bowel disorders, unspecified
[ { "from_icd11": "DD91.Z", "icd10_code": "K598", "icd10_title": "Other specified functional intestinal disorders" }, { "from_icd11": "DD91.Z", "icd10_code": "K599", "icd10_title": "Functional intestinal disorder, unspecified" }, { "from_icd11": "DD91.Z", "icd10_code": "K592", "icd10_title": "Neurogenic bowel, not elsewhere classified" }, { "from_icd11": "DD91.Z", "icd10_code": "K55-K64", "icd10_title": "" }, { "from_icd11": "DD91.Z", "icd10_code": "K59", "icd10_title": "Other functional intestinal disorders" }, { "from_icd11": "9E1Z", "icd10_code": "H5500", "icd10_title": "Unspecified nystagmus" }, { "from_icd11": "9E1Z", "icd10_code": "H5509", "icd10_title": "Other forms of nystagmus" }, { "from_icd11": "9E1Z", "icd10_code": "H5581", "icd10_title": "Saccadic eye movements" }, { "from_icd11": "9E1Z", "icd10_code": "H5501", "icd10_title": "Congenital nystagmus" }, { "from_icd11": "9E1Z", "icd10_code": "H5502", "icd10_title": "Latent nystagmus" }, { "from_icd11": "9E1Z", "icd10_code": "H5589", "icd10_title": "Other irregular eye movements" }, { "from_icd11": "9E1Z", "icd10_code": "H5503", "icd10_title": "Visual deprivation nystagmus" }, { "from_icd11": "9E1Z", "icd10_code": "H5504", "icd10_title": "Dissociated nystagmus" }, { "from_icd11": "9E1Z", "icd10_code": "H44522", "icd10_title": "Atrophy of globe, left eye" }, { "from_icd11": "9E1Z", "icd10_code": "H3552", "icd10_title": "Pigmentary retinal dystrophy" } ]
K598
Other specified functional intestinal disorders
Given the clear diagnosis of ADHD in the child, she was treated with methylphenidate, starting at a dose of 18 mg/day, which was gradually increased to 36 mg/day based on her attentional performance, while also undergoing physical and language rehabilitation training. Additionally, the pediatrician advised the parents to engage the child in reading and retelling stories at home daily. The parents were fully involved in the treatment process. During the first year of treatment, the parents reported a positive impact, and the child's teacher noted an improvement in her attention span and the speed of completing homework. However, in the second year of treatment, both parents and the teacher reported that the child had difficulty concentrating again and exhibited learning difficulties, prompting an increase in the methylphenidate dose to 45 mg/day. This led to difficulties in falling asleep at night and poor sleep quality, so the dose was reduced back to 36 mg/day ( Table 1 ). After two years of regular treatment, the child still met the diagnostic criteria for ADHD. Therefore, this suggests that methylphenidate was not effective in treating the child, and given her comorbid conditions, the possibility of inherited metabolic diseases should be considered. To further investigate the etiology and guide treatment, after obtaining informed consent from the parents, we conducted whole exome sequencing.
4.007813
0.932129
sec[4]/p[0]
en
0.999997
PMC11703840
https://doi.org/10.3389/fped.2024.1500152
[ "parents", "methylphenidate", "adhd", "teacher", "that", "difficulties", "this", "clear", "treated", "starting" ]
[ { "code": "QE50.4", "title": "Relationship with parents, in-laws or other family members" }, { "code": "QE52.1", "title": "Loss of love relationship in childhood" }, { "code": "QE9Y", "title": "Other specified problems associated with upbringing" }, { "code": "QE52.0", "title": "Caregiver-child relationship problem" }, { "code": "QE95", "title": "Inappropriate parental pressure or other abnormal qualities of upbringing" }, { "code": "PB22&XM1NX2", "title": "Unintentional exposure to or harmful effects of methylphenidate" }, { "code": "PC92&XM1NX2", "title": "Intentional self-harm by exposure to or harmful effects of methylphenidate" }, { "code": "PE82&XM1NX2", "title": "Assault by exposure to or harmful effects of methylphenidate" }, { "code": "NE60", "title": "Harmful effects of drugs, medicaments or biological substances, not elsewhere classified" }, { "code": "PH42&XM1NX2", "title": "Harmful effects of or exposure to noxious substances, drugs, medicaments or biological substances, psychostimulants, methylphenidate, undetermined intent" } ]
=== ICD-11 CODES FOUND === [QE50.4] Relationship with parents, in-laws or other family members Also known as: Relationship with parents, in-laws or other family members | Problems in relationship with parents | problem with parent | Problem with aged parent | Problem with sibling Excludes: Caregiver-child relationship problem | Problems associated with upbringing | Problem associated with interactions with spouse or partner [QE52.1] Loss of love relationship in childhood Definition: Loss of an emotionally close relationship, such as of a parent, a sibling, a very special friend or a loved pet, by death or permanent departure or rejection. Also known as: Loss of love relationship in childhood | negative life event in childhood of loss of love relationship | life event in childhood of loss of love relationship | Loss of parent in childhood [QE9Y] Other specified problems associated with upbringing Also known as: Other specified problems associated with upbringing | Lack of learning or play experience | Problem with a parenting situation | problem with atypical parenting situation [QE52.0] Caregiver-child relationship problem Definition: Substantial and sustained dissatisfaction within a caregiver-child relationship, including a parental relationship, associated with significant disturbance in functioning. Also known as: Caregiver-child relationship problem | parent-child relationship problem | Caregiver-child relationship problem with current caregiver | Caregiver-child relationship problem with former caregiver [QE95] Inappropriate parental pressure or other abnormal qualities of upbringing Definition: Parents forcing the child to be different from the local norm, either sex-inappropriate (e.g. dressing a boy in girl's clothes), age-inappropriate (e.g. forcing a child to take on responsibilities above her or his own age) or otherwise inappropriate (e.g. pressing the child to engage in unwanted or too difficult activities). Also known as: Inappropriate parental pressure or other abnormal qualities of upbringing | problem of inappropriate parental pressure [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 === GRAPH WALKS === --- Walk 1 --- [QE50.4] Relationship with parents, in-laws or other family members --EXCLUDES--> [?] Problem associated with interactions with spouse or partner --CHILD--> [?] Relationship distress with spouse or partner Def: Substantial and sustained dissatisfaction with a spouse or intimate partner associated with significant disturbance in functioning.... --- Walk 2 --- [QE50.4] Relationship with parents, in-laws or other family members --EXCLUDES--> [?] Caregiver-child relationship problem Def: Substantial and sustained dissatisfaction within a caregiver-child relationship, including a parental relationship, associated with significant disturbance in functioning.... --CHILD--> [?] Caregiver-child relationship problem with former caregiver Def: Substantial and sustained dissatisfaction within a relationship between a child and a former caregiver, including a parent, associated with significant disturbance in functioning.... --- Walk 3 --- [QE52.1] Loss of love relationship in childhood Def: Loss of an emotionally close relationship, such as of a parent, a sibling, a very special friend or a loved pet, by death or permanent departure or rejection.... --PARENT--> [QE52] Problem associated with interpersonal interactions in childhood --CHILD--> [QE52.1] Loss of love relationship in childhood Def: Loss of an emotionally close relationship, such as of a parent, a sibling, a very special friend or a loved pet, by death or permanent departure or rejection.... --- Walk 4 --- [QE52.1] Loss of love relationship in childhood Def: Loss of an emotionally close relationship, such as of a parent, a sibling, a very special friend or a loved pet, by death or permanent departure or rejection.... --PARENT--> [QE52] Problem associated with interpersonal interactions in childhood --PARENT--> [?] Problems associated with relationships --- Walk 5 --- [QE9Y] Other specified problems associated with upbringing --PARENT--> [?] Problems associated with upbringing --CHILD--> [QE92] Altered pattern of family relationships in childhood Def: Departure of a family member or arrival of a new person into a family resulting in adverse change in child's relationships. May include new relationship or marriage by a parent, death or illness of a ... --- Walk 6 --- [QE9Y] Other specified problems associated with upbringing --PARENT--> [?] Problems associated with upbringing --PARENT--> [?] Factors influencing health status
[ "[QE50.4] Relationship with parents, in-laws or other family members\n --EXCLUDES--> [?] Problem associated with interactions with spouse or partner\n --CHILD--> [?] Relationship distress with spouse or partner\n Def: Substantial and sustained dissatisfaction with a spouse or intimate partner associated with significant disturbance in functioning....", "[QE50.4] Relationship with parents, in-laws or other family members\n --EXCLUDES--> [?] Caregiver-child relationship problem\n Def: Substantial and sustained dissatisfaction within a caregiver-child relationship, including a parental relationship, associated with significant disturbance in functioning....\n --CHILD--> [?] Caregiver-child relationship problem with former caregiver\n Def: Substantial and sustained dissatisfaction within a relationship between a child and a former caregiver, including a parent, associated with significant disturbance in functioning....", "[QE52.1] Loss of love relationship in childhood\n Def: Loss of an emotionally close relationship, such as of a parent, a sibling, a very special friend or a loved pet, by death or permanent departure or rejection....\n --PARENT--> [QE52] Problem associated with interpersonal interactions in childhood\n --CHILD--> [QE52.1] Loss of love relationship in childhood\n Def: Loss of an emotionally close relationship, such as of a parent, a sibling, a very special friend or a loved pet, by death or permanent departure or rejection....", "[QE52.1] Loss of love relationship in childhood\n Def: Loss of an emotionally close relationship, such as of a parent, a sibling, a very special friend or a loved pet, by death or permanent departure or rejection....\n --PARENT--> [QE52] Problem associated with interpersonal interactions in childhood\n --PARENT--> [?] Problems associated with relationships", "[QE9Y] Other specified problems associated with upbringing\n --PARENT--> [?] Problems associated with upbringing\n --CHILD--> [QE92] Altered pattern of family relationships in childhood\n Def: Departure of a family member or arrival of a new person into a family resulting in adverse change in child's relationships. May include new relationship or marriage by a parent, death or illness of a ...", "[QE9Y] Other specified problems associated with upbringing\n --PARENT--> [?] Problems associated with upbringing\n --PARENT--> [?] Factors influencing health status" ]
QE50.4
Relationship with parents, in-laws or other family members
[ { "from_icd11": "QE50.4", "icd10_code": "Z601", "icd10_title": "" }, { "from_icd11": "QE50.4", "icd10_code": "Z631", "icd10_title": "Problems in relationship with in-laws" }, { "from_icd11": "QE52.1", "icd10_code": "Z610", "icd10_title": "" }, { "from_icd11": "QE95", "icd10_code": "Z626", "icd10_title": "Inappropriate (excessive) parental pressure" }, { "from_icd11": "NE60", "icd10_code": "T50A95A", "icd10_title": "Adverse effect of other bacterial vaccines, initial encounter" }, { "from_icd11": "NE60", "icd10_code": "T50Z15A", "icd10_title": "Adverse effect of immunoglobulin, initial encounter" }, { "from_icd11": "NE60", "icd10_code": "T50Z95A", "icd10_title": "Adverse effect of other vaccines and biological substances, initial encounter" }, { "from_icd11": "NE60", "icd10_code": "T50A95S", "icd10_title": "Adverse effect of other bacterial vaccines, sequela" }, { "from_icd11": "NE60", "icd10_code": "T50B95A", "icd10_title": "Adverse effect of other viral vaccines, initial encounter" }, { "from_icd11": "NE60", "icd10_code": "T50A25A", "icd10_title": "Adverse effect of mixed bacterial vaccines without a pertussis component, initial encounter" }, { "from_icd11": "NE60", "icd10_code": "T50A91A", "icd10_title": "Poisoning by other bacterial vaccines, accidental (unintentional), initial encounter" }, { "from_icd11": "NE60", "icd10_code": "T498X5A", "icd10_title": "Adverse effect of other topical agents, initial encounter" }, { "from_icd11": "NE60", "icd10_code": "T48905A", "icd10_title": "Adverse effect of unspecified agents primarily acting on the respiratory system, initial encounter" }, { "from_icd11": "NE60", "icd10_code": "T48995A", "icd10_title": "Adverse effect of other agents primarily acting on the respiratory system, initial encounter" }, { "from_icd11": "NE60", "icd10_code": "T50A15A", "icd10_title": "Adverse effect of pertussis vaccine, including combinations with a pertussis component, initial encounter" } ]
Z601
On examination, she looked skinny and body mass index was 18.49 (156 cm in height and 45 kg in weight). The Mini‐Mental State Examination (MMSE) and Montreal Cognitive Assessment (MoCA) scores were 10 and 6, respectively, suggesting that she had dementia. Facial and appendicular choreatic movements were present. Saccadic eye movements were characterized by variable onset latency and speed. Dysarthria was marked. The basal hormonal evaluation revealed inappropriately low luteinizing hormone (<0.1 mUI/mL), as well as low follicular‐stimulating hormone (1.19 mUI/mL) and estradiol (<18.4 pg/mL). Prolactin and cortisol levels were within normal range. Pelvic echography revealed a postmenopausal uterus (33 × 21 × 35 mm) and the ovaries were not seen. Brain MRI was also performed. The results showed moderate cerebellar atrophy on T1‐weighted image, and extensive bilateral white matter lesions in both cerebral hemispheres, as well as in the brainstem on T2‐weighted fluid‐attenuated inversion recovery image. Susceptibility‐weighted imaging showed no cerebral microbleeds in cortical and subcortical areas . DTI images displayed widespread white matter deterioration as reflected by the decreased fractional anisotropy values and increased radial diffusivity and axial diffusivity values in the voxels of both hemispheres compared with those of controls, while cerebellar white matter fibers relatively spared .
4.105469
0.925781
sec[2]/p[1]
en
0.999998
32358900
https://doi.org/10.1002/acn3.51047
[ "weighted", "white", "matter", "movements", "hormone", "well", "cerebellar", "both", "cerebral", "hemispheres" ]
[ { "code": "MG43.5", "title": "Excessive weight loss" }, { "code": "MG43.6", "title": "Excessive weight gain" }, { "code": "MG44.11", "title": "Failure to thrive in infant or child" }, { "code": "5B80.0Z", "title": "Overweight, unspecified" }, { "code": "JA65.2", "title": "Excessive weight gain in pregnancy" }, { "code": "EF5Y", "title": "Other specified dermatoses attributable to hyperviscosity or microvascular occlusion" }, { "code": "JB41.1", "title": "Deep phlebothrombosis in the puerperium" }, { "code": "EB60.Y", "title": "Lichen sclerosus of other specified sites" }, { "code": "MC80.00", "title": "White coat hypertension" }, { "code": "1F2D.2", "title": "White piedra" } ]
=== ICD-11 CODES FOUND === [MG43.5] Excessive weight loss Definition: A reduction of total body mass, due to loss of fluid, body fat or adipose tissue, or lean (muscle) mass that is sufficient in quantity or rate to create risk to the individual’s health. Also known as: Excessive weight loss | abnormal decrease in weight | abnormal weight loss | unintended weight loss | weight loss NOS [MG43.6] Excessive weight gain Definition: An increase in total body mass, due to increase in fluid, fat or adipose tissue, or lean (muscle) mass that is outside the expected range for normal growth and development and is sufficient in quantity or rate to create risk to the individual’s health. Also known as: Excessive weight gain | abnormal increase in weight | abnormal weight gain | unintended weight gain Excludes: Obesity [MG44.11] Failure to thrive in infant or child Definition: When an infant or child's current weight or rate of weight gain is significantly below that of other children of similar age and gender. Also known as: Failure to thrive in infant or child | failure to gain weight | failure to thrive NOS | FTT - [failure to thrive] syndrome Excludes: Failure to thrive in newborn | Anorexia Nervosa | Avoidant-restrictive food intake disorder [5B80.0Z] Overweight, unspecified Also known as: Overweight, unspecified | Overweight [JA65.2] Excessive weight gain in pregnancy Definition: Any reason for encounter to assess (or care for) a mother for excessive weight gain during pregnancy. Also known as: Excessive weight gain in pregnancy | excessive weight gain in pregnancy, unspecified trimester | maternal obesity syndrome | maternal obesity without hypertension | abnormal weight gain in pregnancy Excludes: Gestational oedema without hypertension [EF5Y] Other specified dermatoses attributable to hyperviscosity or microvascular occlusion Also known as: Other specified dermatoses attributable to hyperviscosity or microvascular occlusion | Cutaneous microvascular occlusion by platelet plugs | Cutaneous microvascular disturbances due to myeloproliferative disorder-associated platelet plugs | Cutaneous microvascular disturbances due to paroxysmal nocturnal haemoglobinuria-associated platelet plugs | Cutaneous microvascular occlusion by emboli [JB41.1] Deep phlebothrombosis in the puerperium Also known as: Deep phlebothrombosis in the puerperium | postnatal deep vein thrombosis | postpartum deep phlebothrombosis | postpartum deep-vein thrombosis | DVT - [deep venous thrombosis] postnatal [EB60.Y] Lichen sclerosus of other specified sites Also known as: Lichen sclerosus of other specified sites | Extragenital lichen sclerosus | Guttate lichen sclerosus | White spot disease | Guttate scleroderma [MC80.00] White coat hypertension Definition: Persistently elevated office blood pressure readings with persistently normal out-of-the-office readings. Also known as: White coat hypertension | white coat syndrome [1F2D.2] White piedra Definition: A disease of the hair shaft, caused by an infection with the fungi Trichosporon beigelii. This disease is characterised by irregular, soft, white, or light brown nodules which adhere to the hair follicle. Transmission is by direct contact with contaminated soil or water, or by airborne transmission. Confirmation is by identification of Trichosporon beigelii in a hair follicle sample. Also known as: White piedra | Trichosporosis nodosa Includes: Trichosporosis nodosa === GRAPH WALKS === --- Walk 1 --- [MG43.5] Excessive weight loss Def: A reduction of total body mass, due to loss of fluid, body fat or adipose tissue, or lean (muscle) mass that is sufficient in quantity or rate to create risk to the individual’s health.... --PARENT--> [MG43] Symptoms or signs concerning food or fluid intake Def: Symptoms or signs concerning food and fluid intake include anorexia, polydipsia, polyphagia, feeding difficulties or mismanagement, abnormal weight loss, abnormal weight gain, insufficient intake of f... --CHILD--> [MG43.2] Abulia Def: Abulia is state of poverty of behaviour and speech output, lack of initiative, loss of emotional responses, psychomotor slowing, and prolonged speech latency.... --- Walk 2 --- [MG43.5] Excessive weight loss Def: A reduction of total body mass, due to loss of fluid, body fat or adipose tissue, or lean (muscle) mass that is sufficient in quantity or rate to create risk to the individual’s health.... --PARENT--> [MG43] Symptoms or signs concerning food or fluid intake Def: Symptoms or signs concerning food and fluid intake include anorexia, polydipsia, polyphagia, feeding difficulties or mismanagement, abnormal weight loss, abnormal weight gain, insufficient intake of f... --CHILD--> [MG43.0] Polydipsia --- Walk 3 --- [MG43.6] Excessive weight gain Def: An increase in total body mass, due to increase in fluid, fat or adipose tissue, or lean (muscle) mass that is outside the expected range for normal growth and development and is sufficient in quantit... --EXCLUDES--> [?] Obesity Def: Obesity is a chronic complex disease defined by excessive adiposity that can impair health. It is in most cases a multifactorial disease due to obesogenic environments, psycho-social factors and genet... --CHILD--> [?] Obesity hypoventilation syndrome Def: 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... --- Walk 4 --- [MG43.6] Excessive weight gain Def: An increase in total body mass, due to increase in fluid, fat or adipose tissue, or lean (muscle) mass that is outside the expected range for normal growth and development and is sufficient in quantit... --RELATED_TO--> [?] Excessive weight gain in pregnancy Def: Any reason for encounter to assess (or care for) a mother for excessive weight gain during pregnancy.... --EXCLUDES--> [?] Gestational oedema without hypertension --- Walk 5 --- [MG44.11] Failure to thrive in infant or child Def: When an infant or child's current weight or rate of weight gain is significantly below that of other children of similar age and gender.... --PARENT--> [MG44.1] Lack of expected normal physiological development Def: Lack of expected normal physiological development includes delayed milestone of development and other lack of expected normal physiological development including gross and fine motor development, lang... --EXCLUDES--> [?] Disorders of intellectual development Def: Disorders of intellectual development are a group of etiologically diverse conditions originating during the developmental period characterised by significantly below average intellectual functioning ... --- Walk 6 --- [MG44.11] Failure to thrive in infant or child Def: When an infant or child's current weight or rate of weight gain is significantly below that of other children of similar age and gender.... --EXCLUDES--> [?] Avoidant-restrictive food intake disorder Def: Avoidant-restrictive food intake disorder (ARFID) is characterised by avoidance or restriction of food intake that results in: 1) the intake of an insufficient quantity or variety of food to meet adeq... --EXCLUDES--> [?] Feeding problems of newborn Def: A lack of interest in feeding or a problem receiving the proper amount of nutrition in a newborn....
[ "[MG43.5] Excessive weight loss\n Def: A reduction of total body mass, due to loss of fluid, body fat or adipose tissue, or lean (muscle) mass that is sufficient in quantity or rate to create risk to the individual’s health....\n --PARENT--> [MG43] Symptoms or signs concerning food or fluid intake\n Def: Symptoms or signs concerning food and fluid intake include anorexia, polydipsia, polyphagia, feeding difficulties or mismanagement, abnormal weight loss, abnormal weight gain, insufficient intake of f...\n --CHILD--> [MG43.2] Abulia\n Def: Abulia is state of poverty of behaviour and speech output, lack of initiative, loss of emotional responses, psychomotor slowing, and prolonged speech latency....", "[MG43.5] Excessive weight loss\n Def: A reduction of total body mass, due to loss of fluid, body fat or adipose tissue, or lean (muscle) mass that is sufficient in quantity or rate to create risk to the individual’s health....\n --PARENT--> [MG43] Symptoms or signs concerning food or fluid intake\n Def: Symptoms or signs concerning food and fluid intake include anorexia, polydipsia, polyphagia, feeding difficulties or mismanagement, abnormal weight loss, abnormal weight gain, insufficient intake of f...\n --CHILD--> [MG43.0] Polydipsia", "[MG43.6] Excessive weight gain\n Def: An increase in total body mass, due to increase in fluid, fat or adipose tissue, or lean (muscle) mass that is outside the expected range for normal growth and development and is sufficient in quantit...\n --EXCLUDES--> [?] Obesity\n Def: Obesity is a chronic complex disease defined by excessive adiposity that can impair health. It is in most cases a multifactorial disease due to obesogenic environments, psycho-social factors and genet...\n --CHILD--> [?] Obesity hypoventilation syndrome\n Def: 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...", "[MG43.6] Excessive weight gain\n Def: An increase in total body mass, due to increase in fluid, fat or adipose tissue, or lean (muscle) mass that is outside the expected range for normal growth and development and is sufficient in quantit...\n --RELATED_TO--> [?] Excessive weight gain in pregnancy\n Def: Any reason for encounter to assess (or care for) a mother for excessive weight gain during pregnancy....\n --EXCLUDES--> [?] Gestational oedema without hypertension", "[MG44.11] Failure to thrive in infant or child\n Def: When an infant or child's current weight or rate of weight gain is significantly below that of other children of similar age and gender....\n --PARENT--> [MG44.1] Lack of expected normal physiological development\n Def: Lack of expected normal physiological development includes delayed milestone of development and other lack of expected normal physiological development including gross and fine motor development, lang...\n --EXCLUDES--> [?] Disorders of intellectual development\n Def: Disorders of intellectual development are a group of etiologically diverse conditions originating during the developmental period characterised by significantly below average intellectual functioning ...", "[MG44.11] Failure to thrive in infant or child\n Def: When an infant or child's current weight or rate of weight gain is significantly below that of other children of similar age and gender....\n --EXCLUDES--> [?] Avoidant-restrictive food intake disorder\n Def: Avoidant-restrictive food intake disorder (ARFID) is characterised by avoidance or restriction of food intake that results in: 1) the intake of an insufficient quantity or variety of food to meet adeq...\n --EXCLUDES--> [?] Feeding problems of newborn\n Def: A lack of interest in feeding or a problem receiving the proper amount of nutrition in a newborn...." ]
MG43.5
Excessive weight loss
[ { "from_icd11": "MG43.5", "icd10_code": "R634", "icd10_title": "Abnormal weight loss" }, { "from_icd11": "MG43.6", "icd10_code": "R635", "icd10_title": "Abnormal weight gain" }, { "from_icd11": "5B80.0Z", "icd10_code": "E669", "icd10_title": "Obesity, unspecified" }, { "from_icd11": "JA65.2", "icd10_code": "O2603", "icd10_title": "Excessive weight gain in pregnancy, third trimester" }, { "from_icd11": "JA65.2", "icd10_code": "O2601", "icd10_title": "Excessive weight gain in pregnancy, first trimester" }, { "from_icd11": "JA65.2", "icd10_code": "O2602", "icd10_title": "Excessive weight gain in pregnancy, second trimester" }, { "from_icd11": "JA65.2", "icd10_code": "O260", "icd10_title": "Excessive weight gain in pregnancy" }, { "from_icd11": "JB41.1", "icd10_code": "O871", "icd10_title": "Deep phlebothrombosis in the puerperium" }, { "from_icd11": "1F2D.2", "icd10_code": "B362", "icd10_title": "White piedra" } ]
R634
Abnormal weight loss
In case 1, a 3-year-old ate mozzarella cheese in her kindergarten dining room, sitting at a table. The child developed signs of airway obstruction and the teachers tried to give her aid through several back blows with no success. Unfortunately, the Italian school system does not make it mandatory for teachers to attend first aid classes . These guidelines report that in the absence of legislation in this regard, it is strongly recommended to provide for the constant presence of personnel who have followed a first aid course in the school canteens frequented mainly by children. Furthermore, the same guidelines recommend that families and adults responsible for supervising the child (e.g., educators in kindergartens, summer centers, after-school, teachers, babysitters) know the rules regarding food preparation and behavior at the table for the prevention of suffocation from food (for example, in the case of the use of plastic cutlery, ensure that these are hard and resistant); furthermore, families and adults responsible for the child’s supervision should acquire knowledge and skills regarding maneuvers to unblock airways and cardiopulmonary resuscitation. In this case, the Heimlich maneuver and adequate supervision of the child were needed. The child arrived at the hospital emergency department where the physicians declared death from suspected asphyxiation, which was later confirmed by autopsy.
3.326172
0.961426
sec[2]/p[1]
en
0.999997
32629891
https://doi.org/10.3390/ijerph17134700
[ "teachers", "school", "that", "these", "guidelines", "this", "furthermore", "families", "adults", "responsible" ]
[ { "code": "QE50.1Z", "title": "Relationships with teachers or classmates, unspecified" }, { "code": "QE50.1Y", "title": "Other specified relationships with teachers or classmates" }, { "code": "CA0H.2", "title": "Nodules of vocal cords" }, { "code": "QD91", "title": "Problem associated with education unavailable or unattainable" }, { "code": "QD92", "title": "Problem with educational progress" }, { "code": "QE50.10", "title": "Dissatisfaction with school environment" }, { "code": "QA01.0", "title": "Examination for admission to educational institution" }, { "code": "QA03.Y", "title": "Other specified routine general health check-up of defined subpopulation" }, { "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 === [QE50.1Z] Relationships with teachers or classmates, unspecified Also known as: Relationships with teachers or classmates, unspecified | Relationships with teachers or classmates | discord with classmates | discord with teachers [QE50.1Y] Other specified relationships with teachers or classmates Also known as: Other specified relationships with teachers or classmates [CA0H.2] Nodules of vocal cords Also known as: Nodules of vocal cords | chorditis cantorum | nodular chorditis | nodule of the vocal cord | screamer's node [QD91] Problem associated with education unavailable or unattainable Also known as: Problem associated with education unavailable or unattainable | schooling unavailable | schooling unattainable [QD92] Problem with educational progress Also known as: Problem with educational progress | Underachievement in school | problem of underachievement in school | lack of achievement in school | Failed examinations Includes: Underachievement in school Excludes: Disorders of intellectual development [QE50.10] Dissatisfaction with school environment Also known as: Dissatisfaction with school environment | educational maladjustment [QA01.0] Examination for admission to educational institution Also known as: Examination for admission to educational institution | medical examination for admission to school | examination for admission to preschool | medical examination of preschool children for admission to school [QA03.Y] Other specified routine general health check-up of defined subpopulation Also known as: Other specified routine general health check-up of defined subpopulation | Routine medical examination of refugees | Routine medical examination of students | Routine medical examination of preschool children | Routine medical examination of schoolchildren [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 --- [QE50.1Z] Relationships with teachers or classmates, unspecified --PARENT--> [QE50.1] Relationships with teachers or classmates --PARENT--> [QE50] Problem associated with interpersonal interactions --- Walk 2 --- [QE50.1Z] Relationships with teachers or classmates, unspecified --PARENT--> [QE50.1] Relationships with teachers or classmates --PARENT--> [QE50] Problem associated with interpersonal interactions --- Walk 3 --- [QE50.1Y] Other specified relationships with teachers or classmates --PARENT--> [QE50.1] Relationships with teachers or classmates --CHILD--> [QE50.10] Dissatisfaction with school environment --- Walk 4 --- [QE50.1Y] Other specified relationships with teachers or classmates --PARENT--> [QE50.1] Relationships with teachers or classmates --CHILD--> [QE50.1Y] Other specified relationships with teachers or classmates --- Walk 5 --- [CA0H.2] Nodules of vocal cords --PARENT--> [CA0H] Diseases of vocal cords or larynx, not elsewhere classified --EXCLUDES--> [?] Acute obstructive laryngitis Def: A condition commonly caused by an acute viral infection of the upper airway. This condition is characterised by a barking cough, stridor, hoarseness, or difficulty breathing. Transmission is commonly ... --- Walk 6 --- [CA0H.2] Nodules of vocal cords --PARENT--> [CA0H] Diseases of vocal cords or larynx, not elsewhere classified --EXCLUDES--> [?] Stridor Def: Stridor or a low-pitched, focal inspiratory wheeze usually heard over the neck is a manifestation of upper airway obstruction and should result in an expedited evaluation of the patient as it can prec...
[ "[QE50.1Z] Relationships with teachers or classmates, unspecified\n --PARENT--> [QE50.1] Relationships with teachers or classmates\n --PARENT--> [QE50] Problem associated with interpersonal interactions", "[QE50.1Z] Relationships with teachers or classmates, unspecified\n --PARENT--> [QE50.1] Relationships with teachers or classmates\n --PARENT--> [QE50] Problem associated with interpersonal interactions", "[QE50.1Y] Other specified relationships with teachers or classmates\n --PARENT--> [QE50.1] Relationships with teachers or classmates\n --CHILD--> [QE50.10] Dissatisfaction with school environment", "[QE50.1Y] Other specified relationships with teachers or classmates\n --PARENT--> [QE50.1] Relationships with teachers or classmates\n --CHILD--> [QE50.1Y] Other specified relationships with teachers or classmates", "[CA0H.2] Nodules of vocal cords\n --PARENT--> [CA0H] Diseases of vocal cords or larynx, not elsewhere classified\n --EXCLUDES--> [?] Acute obstructive laryngitis\n Def: A condition commonly caused by an acute viral infection of the upper airway. This condition is characterised by a barking cough, stridor, hoarseness, or difficulty breathing. Transmission is commonly ...", "[CA0H.2] Nodules of vocal cords\n --PARENT--> [CA0H] Diseases of vocal cords or larynx, not elsewhere classified\n --EXCLUDES--> [?] Stridor\n Def: Stridor or a low-pitched, focal inspiratory wheeze usually heard over the neck is a manifestation of upper airway obstruction and should result in an expedited evaluation of the patient as it can prec..." ]
QE50.1Z
Relationships with teachers or classmates, unspecified
[ { "from_icd11": "QE50.1Z", "icd10_code": "Z554", "icd10_title": "Educational maladjustment and discord with teachers and classmates" }, { "from_icd11": "CA0H.2", "icd10_code": "J382", "icd10_title": "Nodules of vocal cords" }, { "from_icd11": "QD91", "icd10_code": "Z551", "icd10_title": "Schooling unavailable and unattainable" }, { "from_icd11": "QD92", "icd10_code": "Z553", "icd10_title": "Underachievement in school" }, { "from_icd11": "QD92", "icd10_code": "Z552", "icd10_title": "Failed school examinations" }, { "from_icd11": "QA01.0", "icd10_code": "Z020", "icd10_title": "Encounter for examination for admission to educational institution" }, { "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" } ]
Z554
Educational maladjustment and discord with teachers and classmates
Most reported cases of orbital emphysema follow a history of trauma, though not necessarily immediately . Patients with a preceding episode of trauma days or weeks before may present acutely with orbital emphysema after an episode of increased intranasal pressure provoked by sneezing or nose-blowing. However, in this case, there was no preceding injury noted. From a review of the literature, we have identified only 21 cases of orbital emphysema where no history of trauma or periocular surgery was evident [ 8 – 28 ]. Cases of orbital emphysema are usually mild and do not affect visual function, with approximately 12% of patients requiring decompression . Of the 21 cases found with no history of trauma [ 8 – 28 ], one had nonurgent surgery due to persistent diplopia lasting more than a week . In this case, fractures of the orbital floor were apparent, with fat entrapment. Two of the 21 cases reported emergency needle decompression . In the first, there was proptosis, restriction of eye movements, raised intraocular pressure (IOP), and a hazy cornea. However, it was noted that there was no RAPD or dyschromatopsia and therefore no evidence of optic nerve compromise. In the second, decompression was performed due to the extent of eyelid swelling precluding assessment of the eye. As such, our case is the first to document clear evidence of optic nerve dysfunction after nontraumatic orbital emphysema.
4.191406
0.788574
sec[2]/p[0]
en
0.999997
33777467
https://doi.org/10.1155/2021/8884009
[ "orbital", "cases", "emphysema", "trauma", "decompression", "patients", "preceding", "episode", "pressure", "however" ]
[ { "code": "9A2Z", "title": "Disorders of orbit, unspecified" }, { "code": "9A22.Z", "title": "Orbital inflammation, unspecified" }, { "code": "9A2Y", "title": "Other specified disorders of orbit" }, { "code": "LA14.2", "title": "Structural developmental anomalies of orbit" }, { "code": "9A24.0", "title": "Contraction of orbit" }, { "code": "JB20.Z", "title": "Single spontaneous delivery, unspecified" }, { "code": "QA48.0", "title": "Care or examination immediately after delivery" }, { "code": "CA21.Z", "title": "Emphysema, unspecified" }, { "code": "CA21.Y", "title": "Other specified emphysema" }, { "code": "KB27.0", "title": "Interstitial emphysema originating in the perinatal period" } ]
=== ICD-11 CODES FOUND === [9A2Z] Disorders of orbit, unspecified Also known as: Disorders of orbit, unspecified [9A22.Z] Orbital inflammation, unspecified Also known as: Orbital inflammation, unspecified | Orbital inflammation | inflammation of orbit | Acute inflammation of orbit | acute orbital inflammation [9A2Y] Other specified disorders of orbit Also known as: Other specified disorders of orbit | Orbital deformity | deformity of orbit proper | Atrophy of orbit [LA14.2] Structural developmental anomalies of orbit Definition: Any condition caused by failure of the orbit to correctly develop during the antenatal period. Also known as: Structural developmental anomalies of orbit | congenital anomaly of orbit | congenital anomaly of orbit proper | specified congenital anomalies of orbit | anomaly of orbit [9A24.0] Contraction of orbit Also known as: Contraction of orbit | Posttrauma contraction of orbit | Postradiation contraction of orbit | Postsurgery contraction of orbit [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 [CA21.Z] Emphysema, unspecified Also known as: Emphysema, unspecified | Emphysema | emphysema of lung | pulmonary emphysema | pulmonary emphysema NOS [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 [KB27.0] Interstitial emphysema originating in the perinatal period Definition: Escape of air into the interstitium, lymphatics and venous circulation of the lungs resulting from rupture of small airways associated with a characteristic cystic appearance on chest X-ray, almost exclusively seen in preterm infants receiving mechanical ventilation Also known as: Interstitial emphysema originating in the perinatal period | congenital interstitial emphysema | interstitial emphysema, perinatal period | congenital pulmonary emphysema | congenital emphysema === GRAPH WALKS === --- Walk 1 --- [9A2Z] Disorders of orbit, unspecified --PARENT--> [?] Disorders of orbit Def: This refers to disorders of the cavity or socket of the skull in which the eye and its appendages are situated. "Orbit" can refer to the bony socket, or it can also be used to imply the contents.... --RELATED_TO--> [?] Structural developmental anomalies of orbit Def: Any condition caused by failure of the orbit to correctly develop during the antenatal period.... --- Walk 2 --- [9A2Z] Disorders of orbit, unspecified --PARENT--> [?] Disorders of orbit Def: This refers to disorders of the cavity or socket of the skull in which the eye and its appendages are situated. "Orbit" can refer to the bony socket, or it can also be used to imply the contents.... --CHILD--> [9A21] Orbital infection --- Walk 3 --- [9A22.Z] Orbital inflammation, unspecified --PARENT--> [9A22] Orbital inflammation --CHILD--> [9A22.1] Diffuse orbital inflammation --- Walk 4 --- [9A22.Z] Orbital inflammation, unspecified --PARENT--> [9A22] Orbital inflammation --CHILD--> [9A22.1] Diffuse orbital inflammation --- Walk 5 --- [9A2Y] Other specified disorders of orbit --PARENT--> [?] Disorders of orbit Def: This refers to disorders of the cavity or socket of the skull in which the eye and its appendages are situated. "Orbit" can refer to the bony socket, or it can also be used to imply the contents.... --CHILD--> [9A21] Orbital infection --- Walk 6 --- [9A2Y] Other specified disorders of orbit --PARENT--> [?] Disorders of orbit Def: This refers to disorders of the cavity or socket of the skull in which the eye and its appendages are situated. "Orbit" can refer to the bony socket, or it can also be used to imply the contents.... --RELATED_TO--> [?] Structural developmental anomalies of orbit Def: Any condition caused by failure of the orbit to correctly develop during the antenatal period....
[ "[9A2Z] Disorders of orbit, unspecified\n --PARENT--> [?] Disorders of orbit\n Def: This refers to disorders of the cavity or socket of the skull in which the eye and its appendages are situated. \"Orbit\" can refer to the bony socket, or it can also be used to imply the contents....\n --RELATED_TO--> [?] Structural developmental anomalies of orbit\n Def: Any condition caused by failure of the orbit to correctly develop during the antenatal period....", "[9A2Z] Disorders of orbit, unspecified\n --PARENT--> [?] Disorders of orbit\n Def: This refers to disorders of the cavity or socket of the skull in which the eye and its appendages are situated. \"Orbit\" can refer to the bony socket, or it can also be used to imply the contents....\n --CHILD--> [9A21] Orbital infection", "[9A22.Z] Orbital inflammation, unspecified\n --PARENT--> [9A22] Orbital inflammation\n --CHILD--> [9A22.1] Diffuse orbital inflammation", "[9A22.Z] Orbital inflammation, unspecified\n --PARENT--> [9A22] Orbital inflammation\n --CHILD--> [9A22.1] Diffuse orbital inflammation", "[9A2Y] Other specified disorders of orbit\n --PARENT--> [?] Disorders of orbit\n Def: This refers to disorders of the cavity or socket of the skull in which the eye and its appendages are situated. \"Orbit\" can refer to the bony socket, or it can also be used to imply the contents....\n --CHILD--> [9A21] Orbital infection", "[9A2Y] Other specified disorders of orbit\n --PARENT--> [?] Disorders of orbit\n Def: This refers to disorders of the cavity or socket of the skull in which the eye and its appendages are situated. \"Orbit\" can refer to the bony socket, or it can also be used to imply the contents....\n --RELATED_TO--> [?] Structural developmental anomalies of orbit\n Def: Any condition caused by failure of the orbit to correctly develop during the antenatal period...." ]
9A2Z
Disorders of orbit, unspecified
[ { "from_icd11": "9A2Z", "icd10_code": "H0589", "icd10_title": "Other disorders of orbit" }, { "from_icd11": "9A2Z", "icd10_code": "H05339", "icd10_title": "Deformity of unspecified orbit due to trauma or surgery" }, { "from_icd11": "9A2Z", "icd10_code": "H05819", "icd10_title": "Cyst of unspecified orbit" }, { "from_icd11": "9A2Z", "icd10_code": "H059", "icd10_title": "Unspecified disorder of orbit" }, { "from_icd11": "9A2Z", "icd10_code": "H05", "icd10_title": "Disorders of orbit" }, { "from_icd11": "9A2Z", "icd10_code": "H053", "icd10_title": "Deformity of orbit" }, { "from_icd11": "9A2Z", "icd10_code": "H055", "icd10_title": "Retained (old) foreign body following penetrating wound of orbit" }, { "from_icd11": "9A2Z", "icd10_code": "H058", "icd10_title": "Other disorders of orbit" }, { "from_icd11": "9A2Z", "icd10_code": "H06", "icd10_title": "" }, { "from_icd11": "9A2Z", "icd10_code": "H063", "icd10_title": "" }, { "from_icd11": "9A22.Z", "icd10_code": "H05012", "icd10_title": "Cellulitis of left orbit" }, { "from_icd11": "9A22.Z", "icd10_code": "H05011", "icd10_title": "Cellulitis of right orbit" }, { "from_icd11": "9A22.Z", "icd10_code": "H05022", "icd10_title": "Osteomyelitis of left orbit" }, { "from_icd11": "9A22.Z", "icd10_code": "H05111", "icd10_title": "Granuloma of right orbit" }, { "from_icd11": "9A22.Z", "icd10_code": "H05019", "icd10_title": "Cellulitis of unspecified orbit" } ]
H0589
Other disorders of orbit
This case shows a possible association between an incomplete double ureter, arching testicular arteries and an accessory testicular artery. To our knowledge, this report is the first to identify and describe the coexistence of these anomalies and their possible clinical implications. Both double ureter and these arterial anomalies can cause urological symptoms and therefore must be distinguished. Furthermore, arching testicular arteries may cause nutcracker syndrome and should be especially considered as a possible cause when work-up reveals no compression by the SMA. This possible etiology of nutcracker syndrome has been suggested in at least several articles but has not been studied in depth or proven to exist. This case report highlights the possible association between three examples of CAKUT and therefore, unlike other articles, proposes that one look twice after finding an anomaly in order to detect other variations and correctly identify the root cause of the patient’s symptoms. Our report contributes to the limited literature and highlights the importance of reporting these anomalies when encountered during autopsies or pedagogical cadaveric dissection. A comprehensive understanding and identification of variations in testicular vessels and renal structures, along with considering potentially associated complications, are essential for accurate diagnosis and safe surgical interventions.
4.113281
0.945313
sec[3]/p[0]
en
0.999997
39310392
https://doi.org/10.7759/cureus.67613
[ "possible", "this", "testicular", "cause", "these", "anomalies", "association", "double", "ureter", "arching" ]
[ { "code": "QA86", "title": "Problem with isolation protocol without injury or harm" }, { "code": "6B41", "title": "Complex post traumatic stress disorder" }, { "code": "JA8Z", "title": "Maternal care related to unspecified fetus, amniotic cavity or possible delivery problems" }, { "code": "JA8Y", "title": "Maternal care related to other specified fetus, amniotic cavity or possible delivery problems" }, { "code": "4A01.03", "title": "Transient hypogammaglobulinaemia of infancy" }, { "code": "GB0Y&XA4947", "title": "Disease or disorder of testis, unspecified" }, { "code": "GB02.1&XA4947", "title": "Inflammation of testis" }, { "code": "LB51", "title": "Anorchia or microorchidia" }, { "code": "GB03", "title": "Atrophy of testis" }, { "code": "2F97&XA4947", "title": "Neoplasms of unknown behaviour of testis" } ]
=== ICD-11 CODES FOUND === [QA86] Problem with isolation protocol without injury or harm Definition: Patient not monitored as frequently as required or ordered; or patient mistakenly or inappropriately put on isolation; or isolation technique broken and contamination possible by patient, health provider, or visitor. No injury or harm resulted. Also known as: Problem with isolation protocol without injury or harm | isolation technique broken and contamination possible without documented injury or harm | patient mistakenly or inappropriately put on isolation without documented injury or harm | Patient not monitored as frequently as required or ordered without documented injury or harm Excludes: Problem associated with isolation protocol [6B41] Complex post traumatic stress disorder Definition: Complex post traumatic stress disorder (Complex PTSD) is a disorder that may develop following exposure to an event or series of events of an extremely threatening or horrific nature, most commonly prolonged or repetitive events from which escape is difficult or impossible (e.g. torture, slavery, genocide campaigns, prolonged domestic violence, repeated childhood sexual or physical abuse). All diagnostic requirements for PTSD are met. In addition, Complex PTSD is characterised by severe and pers Also known as: Complex post traumatic stress disorder | enduring personality change after catastrophic experience | complex PTSD | personality change after disasters | Personality change after concentration camp experiences Excludes: Post traumatic stress disorder | Personality disorder [JA8Z] Maternal care related to unspecified fetus, amniotic cavity or possible delivery problems Also known as: Maternal care related to unspecified fetus, amniotic cavity or possible delivery problems [JA8Y] Maternal care related to other specified fetus, amniotic cavity or possible delivery problems Also known as: Maternal care related to other specified fetus, amniotic cavity or possible delivery problems [4A01.03] Transient hypogammaglobulinaemia of infancy Also known as: Transient hypogammaglobulinaemia of infancy | immunoglobulin maturational delay | THI - [transient hypogammaglobulinaemia of infancy] [LB51] Anorchia or microorchidia Definition: A disorder affecting males, caused by an abnormality occurring in sex development during the antenatal period. This disorder is characterised by individuals who are born with absence of the testes, or with testes that are deficient in size and function. Confirmation is by physical examination, identification of low testosterone levels but elevated follicle stimulating hormone and luteinizing hormone levels in a blood sample, or imaging. Also known as: Anorchia or microorchidia | Absence or aplasia of testis, unilateral | congenital absence of testis, unilateral | congenital absent testicle | congenital absence of testis [GB03] Atrophy of testis Definition: A condition of the testis, caused by apoptosis of the cells due to diminished cellular proliferation, decreased cellular volume, decreased function, ischemia, malnutrition, disease, infection, mutation, or hormonal changes. This condition is characterised by a partial or complete decrease in size and function of the testis tissue. Also known as: Atrophy of testis | atrophic testicle | atrophy of testicle | testicular atrophy === GRAPH WALKS === --- Walk 1 --- [QA86] Problem with isolation protocol without injury or harm Def: Patient not monitored as frequently as required or ordered; or patient mistakenly or inappropriately put on isolation; or isolation technique broken and contamination possible by patient, health provi... --EXCLUDES--> [?] Problem associated with isolation protocol Def: Isolation of patient for infection cause injury to occur... --PARENT--> [?] Mode of injury or harm associated with other health care related causes --- Walk 2 --- [QA86] Problem with isolation protocol without injury or harm Def: Patient not monitored as frequently as required or ordered; or patient mistakenly or inappropriately put on isolation; or isolation technique broken and contamination possible by patient, health provi... --EXCLUDES--> [?] Problem associated with isolation protocol Def: Isolation of patient for infection cause injury to occur... --PARENT--> [?] Mode of injury or harm associated with other health care related causes --- Walk 3 --- [6B41] Complex post traumatic stress disorder Def: Complex post traumatic stress disorder (Complex PTSD) is a disorder that may develop following exposure to an event or series of events of an extremely threatening or horrific nature, most commonly pr... --EXCLUDES--> [?] Post traumatic stress disorder Def: Post traumatic stress disorder (PTSD) may develop following exposure to an extremely threatening or horrific event or series of events. It is characterised by all of the following: 1) re-experiencing ... --CHILD--> [?] Battered person syndrome --- Walk 4 --- [6B41] Complex post traumatic stress disorder Def: Complex post traumatic stress disorder (Complex PTSD) is a disorder that may develop following exposure to an event or series of events of an extremely threatening or horrific nature, most commonly pr... --EXCLUDES--> [?] Personality disorder Def: Personality disorder is characterised by problems in functioning of aspects of the self (e.g., identity, self-worth, accuracy of self-view, self-direction), and/or interpersonal dysfunction (e.g., abi... --CHILD--> [?] Mild personality disorder Def: All general diagnostic requirements for Personality Disorder are met. Disturbances affect some areas of personality functioning but not others (e.g., problems with self-direction in the absence of pro... --- Walk 5 --- [JA8Z] Maternal care related to unspecified fetus, amniotic cavity or possible delivery problems --PARENT--> [?] Maternal care related to the fetus, amniotic cavity or possible delivery problems Def: A group of conditions characterised by the provision of health interventions to the mother due to conditions associated with the fetus, the amniotic cavity, or to issues associated with labour and del... --CHILD--> [JA82] Maternal care for malpresentation of fetus Def: Care provided for the pregnant female for incorrect position or orientation of the fetus at near term or during labour, determined by its relation to the spine of the mother and the birth canal.... --- Walk 6 --- [JA8Z] Maternal care related to unspecified fetus, amniotic cavity or possible delivery problems --PARENT--> [?] Maternal care related to the fetus, amniotic cavity or possible delivery problems Def: A group of conditions characterised by the provision of health interventions to the mother due to conditions associated with the fetus, the amniotic cavity, or to issues associated with labour and del... --CHILD--> [JA82] Maternal care for malpresentation of fetus Def: Care provided for the pregnant female for incorrect position or orientation of the fetus at near term or during labour, determined by its relation to the spine of the mother and the birth canal....
[ "[QA86] Problem with isolation protocol without injury or harm\n Def: Patient not monitored as frequently as required or ordered; or patient mistakenly or inappropriately put on isolation; or isolation technique broken and contamination possible by patient, health provi...\n --EXCLUDES--> [?] Problem associated with isolation protocol\n Def: Isolation of patient for infection cause injury to occur...\n --PARENT--> [?] Mode of injury or harm associated with other health care related causes", "[QA86] Problem with isolation protocol without injury or harm\n Def: Patient not monitored as frequently as required or ordered; or patient mistakenly or inappropriately put on isolation; or isolation technique broken and contamination possible by patient, health provi...\n --EXCLUDES--> [?] Problem associated with isolation protocol\n Def: Isolation of patient for infection cause injury to occur...\n --PARENT--> [?] Mode of injury or harm associated with other health care related causes", "[6B41] Complex post traumatic stress disorder\n Def: Complex post traumatic stress disorder (Complex PTSD) is a disorder that may develop following exposure to an event or series of events of an extremely threatening or horrific nature, most commonly pr...\n --EXCLUDES--> [?] Post traumatic stress disorder\n Def: Post traumatic stress disorder (PTSD) may develop following exposure to an extremely threatening or horrific event or series of events. It is characterised by all of the following: 1) re-experiencing ...\n --CHILD--> [?] Battered person syndrome", "[6B41] Complex post traumatic stress disorder\n Def: Complex post traumatic stress disorder (Complex PTSD) is a disorder that may develop following exposure to an event or series of events of an extremely threatening or horrific nature, most commonly pr...\n --EXCLUDES--> [?] Personality disorder\n Def: Personality disorder is characterised by problems in functioning of aspects of the self (e.g., identity, self-worth, accuracy of self-view, self-direction), and/or interpersonal dysfunction (e.g., abi...\n --CHILD--> [?] Mild personality disorder\n Def: All general diagnostic requirements for Personality Disorder are met. Disturbances affect some areas of personality functioning but not others (e.g., problems with self-direction in the absence of pro...", "[JA8Z] Maternal care related to unspecified fetus, amniotic cavity or possible delivery problems\n --PARENT--> [?] Maternal care related to the fetus, amniotic cavity or possible delivery problems\n Def: A group of conditions characterised by the provision of health interventions to the mother due to conditions associated with the fetus, the amniotic cavity, or to issues associated with labour and del...\n --CHILD--> [JA82] Maternal care for malpresentation of fetus\n Def: Care provided for the pregnant female for incorrect position or orientation of the fetus at near term or during labour, determined by its relation to the spine of the mother and the birth canal....", "[JA8Z] Maternal care related to unspecified fetus, amniotic cavity or possible delivery problems\n --PARENT--> [?] Maternal care related to the fetus, amniotic cavity or possible delivery problems\n Def: A group of conditions characterised by the provision of health interventions to the mother due to conditions associated with the fetus, the amniotic cavity, or to issues associated with labour and del...\n --CHILD--> [JA82] Maternal care for malpresentation of fetus\n Def: Care provided for the pregnant female for incorrect position or orientation of the fetus at near term or during labour, determined by its relation to the spine of the mother and the birth canal...." ]
QA86
Problem with isolation protocol without injury or harm
[ { "from_icd11": "QA86", "icd10_code": "XXI", "icd10_title": "" }, { "from_icd11": "6B41", "icd10_code": "F62", "icd10_title": "" }, { "from_icd11": "6B41", "icd10_code": "F620", "icd10_title": "" }, { "from_icd11": "JA8Z", "icd10_code": "O30-O48", "icd10_title": "" }, { "from_icd11": "4A01.03", "icd10_code": "D807", "icd10_title": "Transient hypogammaglobulinemia of infancy" }, { "from_icd11": "LB51", "icd10_code": "Q550", "icd10_title": "Absence and aplasia of testis" }, { "from_icd11": "LB51", "icd10_code": "Q55", "icd10_title": "Other congenital malformations of male genital organs" }, { "from_icd11": "GB03", "icd10_code": "N503", "icd10_title": "Cyst of epididymis" }, { "from_icd11": "GB03", "icd10_code": "N500", "icd10_title": "Atrophy of testis" }, { "from_icd11": "GB03", "icd10_code": "N50", "icd10_title": "Other and unspecified disorders of male genital organs" }, { "from_icd11": "2F97&XA4947", "icd10_code": "D401", "icd10_title": "Neoplasm of uncertain behavior of testis" } ]
XXI
Case 3 . A White man aged 50 years traveled to Burkina Faso for 10 days in November 2017 on a mission trip and did not take malaria prophylaxis. A few weeks after returning, he experienced fever and fatigue but did not seek medical attention. A week after the start of his symptoms, his daughter found him at home with altered mental status and a bruise on his forehead. She took him to an emergency department, where the workup revealed acute kidney injury, jaundice, and a positive malaria smear, with no species or parasitemia reported. A CT scan of the head showed no abnormalities. The patient was administered intravenous clindamycin and early the following day was transferred to another hospital, where he was admitted to the ICU and was given IV quinidine gluconate and IV doxycycline for treatment of severe malaria. Shortly after starting quinidine, a widened QRS complex was observed on an electrocardiogram, and quinidine toxicity was suspected. IV artesunate was requested from CDC and administered. However, the patient’s condition deteriorated, requiring intubation and mechanical ventilation, vasopressor support, and continuous renal replacement therapy for acute kidney injury. The patient died on the eighth day after being hospitalized. The malaria smear at the initial hospital was sent to an outside laboratory, and results available later revealed P. falciparum infection with 16% parasitemia.
3.8125
0.984863
sec[2]/sec[16]/sec[3]/p[3]
en
0.999997
33735166
https://doi.org/10.15585/mmwr.ss7002a1
[ "malaria", "quinidine", "kidney", "injury", "smear", "parasitemia", "white", "traveled", "burkina", "faso" ]
[ { "code": "1F42.Z", "title": "Plasmodium malariae malaria without complication" }, { "code": "1F45", "title": "Malaria without parasitological confirmation" }, { "code": "1F4Z", "title": "Malaria, unspecified" }, { "code": "1F44", "title": "Other parasitologically confirmed malaria" }, { "code": "KA64.Y", "title": "Other specified parasitic diseases in the fetus or newborn" }, { "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 === [1F42.Z] Plasmodium malariae malaria without complication Also known as: Plasmodium malariae malaria without complication | Malaria due to Plasmodium malariae | quartan malaria | quartan ague | quartan fever [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 [1F4Z] Malaria, unspecified Also known as: Malaria, unspecified [1F44] Other parasitologically confirmed malaria Also known as: Other parasitologically confirmed malaria | Parasitologically confirmed malaria NOS | Malaria confirmed | Malaria due to Plasmodium knowlesi | Malaria due to simian plasmodia [KA64.Y] Other specified parasitic diseases in the fetus or newborn Also known as: Other specified parasitic diseases in the fetus or newborn | Other congenital malaria [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 --- [1F42.Z] Plasmodium malariae malaria without complication --PARENT--> [1F42] Malaria due to Plasmodium malariae Def: A disease caused by an infection with the protozoan parasite Plasmodium malariae. This disease is characterised by fever, chills, headache, nausea and vomiting, body aches, or general malaise. Transmi... --EXCLUDES--> [?] Malaria due to Plasmodium vivax Def: A disease caused by an infection with the protozoan parasite Plasmodium vivax. This disease is characterised by fever, chills, headache, nausea and vomiting, body aches, or general malaise. Transmissi... --- Walk 2 --- [1F42.Z] Plasmodium malariae malaria without complication --PARENT--> [1F42] Malaria due to Plasmodium malariae Def: A disease caused by an infection with the protozoan parasite Plasmodium malariae. This disease is characterised by fever, chills, headache, nausea and vomiting, body aches, or general malaise. Transmi... --CHILD--> [1F42.Z] Plasmodium malariae malaria without complication --- Walk 3 --- [1F45] Malaria without parasitological confirmation Def: Clinically diagnosed malaria without parasitological confirmation... --PARENT--> [?] Malaria Def: A disease caused by an infection with a protozoan parasite from the Plasmodium genus. This disease commonly presents with fever, chills, headache, nausea and vomiting, or malaise. Transmission is thro... --RELATED_TO--> [?] HIV disease clinical stage 3 associated with malaria --- Walk 4 --- [1F45] Malaria without parasitological confirmation Def: Clinically diagnosed malaria without parasitological confirmation... --PARENT--> [?] Malaria Def: A disease caused by an infection with a protozoan parasite from the Plasmodium genus. This disease commonly presents with fever, chills, headache, nausea and vomiting, or malaise. Transmission is thro... --RELATED_TO--> [?] HIV disease clinical stage 4 associated with malaria --- Walk 5 --- [1F4Z] Malaria, unspecified --PARENT--> [?] Malaria Def: A disease caused by an infection with a protozoan parasite from the Plasmodium genus. This disease commonly presents with fever, chills, headache, nausea and vomiting, or malaise. Transmission is thro... --CHILD--> [1F42] Malaria due to Plasmodium malariae Def: A disease caused by an infection with the protozoan parasite Plasmodium malariae. This disease is characterised by fever, chills, headache, nausea and vomiting, body aches, or general malaise. Transmi... --- Walk 6 --- [1F4Z] Malaria, unspecified --PARENT--> [?] Malaria Def: A disease caused by an infection with a protozoan parasite from the Plasmodium genus. This disease commonly presents with fever, chills, headache, nausea and vomiting, or malaise. Transmission is thro... --CHILD--> [1F40] Malaria due to Plasmodium falciparum Def: A disease caused by an infection with the protozoan parasite Plasmodium falciparum. This disease is characterised by fever, chills, headache, myalgia, arthralgia, weakness, vomiting, or diarrhoea. Thi...
[ "[1F42.Z] Plasmodium malariae malaria without complication\n --PARENT--> [1F42] Malaria due to Plasmodium malariae\n Def: A disease caused by an infection with the protozoan parasite Plasmodium malariae. This disease is characterised by fever, chills, headache, nausea and vomiting, body aches, or general malaise. Transmi...\n --EXCLUDES--> [?] Malaria due to Plasmodium vivax\n Def: A disease caused by an infection with the protozoan parasite Plasmodium vivax. This disease is characterised by fever, chills, headache, nausea and vomiting, body aches, or general malaise. Transmissi...", "[1F42.Z] Plasmodium malariae malaria without complication\n --PARENT--> [1F42] Malaria due to Plasmodium malariae\n Def: A disease caused by an infection with the protozoan parasite Plasmodium malariae. This disease is characterised by fever, chills, headache, nausea and vomiting, body aches, or general malaise. Transmi...\n --CHILD--> [1F42.Z] Plasmodium malariae malaria without complication", "[1F45] Malaria without parasitological confirmation\n Def: Clinically diagnosed malaria without parasitological confirmation...\n --PARENT--> [?] Malaria\n Def: A disease caused by an infection with a protozoan parasite from the Plasmodium genus. This disease commonly presents with fever, chills, headache, nausea and vomiting, or malaise. Transmission is thro...\n --RELATED_TO--> [?] HIV disease clinical stage 3 associated with malaria", "[1F45] Malaria without parasitological confirmation\n Def: Clinically diagnosed malaria without parasitological confirmation...\n --PARENT--> [?] Malaria\n Def: A disease caused by an infection with a protozoan parasite from the Plasmodium genus. This disease commonly presents with fever, chills, headache, nausea and vomiting, or malaise. Transmission is thro...\n --RELATED_TO--> [?] HIV disease clinical stage 4 associated with malaria", "[1F4Z] Malaria, unspecified\n --PARENT--> [?] Malaria\n Def: A disease caused by an infection with a protozoan parasite from the Plasmodium genus. This disease commonly presents with fever, chills, headache, nausea and vomiting, or malaise. Transmission is thro...\n --CHILD--> [1F42] Malaria due to Plasmodium malariae\n Def: A disease caused by an infection with the protozoan parasite Plasmodium malariae. This disease is characterised by fever, chills, headache, nausea and vomiting, body aches, or general malaise. Transmi...", "[1F4Z] Malaria, unspecified\n --PARENT--> [?] Malaria\n Def: A disease caused by an infection with a protozoan parasite from the Plasmodium genus. This disease commonly presents with fever, chills, headache, nausea and vomiting, or malaise. Transmission is thro...\n --CHILD--> [1F40] Malaria due to Plasmodium falciparum\n Def: A disease caused by an infection with the protozoan parasite Plasmodium falciparum. This disease is characterised by fever, chills, headache, myalgia, arthralgia, weakness, vomiting, or diarrhoea. Thi..." ]
1F42.Z
Plasmodium malariae malaria without complication
[ { "from_icd11": "1F42.Z", "icd10_code": "B528", "icd10_title": "Plasmodium malariae malaria with other complications" }, { "from_icd11": "1F42.Z", "icd10_code": "B52", "icd10_title": "Plasmodium malariae malaria" }, { "from_icd11": "1F42.Z", "icd10_code": "B529", "icd10_title": "Plasmodium malariae malaria without complication" }, { "from_icd11": "1F45", "icd10_code": "B54", "icd10_title": "Unspecified malaria" }, { "from_icd11": "1F4Z", "icd10_code": "B50-B64", "icd10_title": "" }, { "from_icd11": "1F44", "icd10_code": "B538", "icd10_title": "Other malaria, not elsewhere classified" }, { "from_icd11": "1F44", "icd10_code": "B531", "icd10_title": "Malaria due to simian plasmodia" }, { "from_icd11": "1F44", "icd10_code": "B53", "icd10_title": "Other specified malaria" }, { "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" } ]
B528
Plasmodium malariae malaria with other complications
In May 2019, a patient with a clinical history of atrial fibrillation and hypertensive heart disease arrived at a local hospital in Sichuan province. No local or international travel or contact with wildlife or household animals was reported. A meal with rice noodles and raw vegetables outside the hospital was the only significant record for the initial medical history. Acute syndromes of high fever, expiratory dyspnoea, chills and diarrhoea were observed on the next day (Day 2 at 2AM). The patient also complained of headache and abdominal pain. Laboratory investigation indicated an elevated white-blood-cell count (12.97×10 9 /l). Oral berberine and intramuscular injection of gentamicin were given as primary treatment. Two hours later, body temperature had increased to 40 °C, accompanied by watery diarrhoea with tenesmus, nausea and vomiting. Cefoperazone/sulbactam and pantoprazole were administered as new treatment. On Day 3, most syndromes returned to normal, except for nausea, vomiting and watery diarrhoea. On Days 5 and 9, blood and stool samples were collected, respectively. The blood specimen confirmed positive culture for Salmonella , but no Shigella was detected or isolated from either sample. Sustained treatment with cefotaxime and pazufloxacin was given in the next 3 days and the patient recovered. The patient was diagnosed with infectious diarrhoea, complicated by invasive syndromes.
3.771484
0.984863
sec[1]/sec[0]/p[0]
en
0.999996
32589568
https://doi.org/10.1099/mgen.0.000401
[ "diarrhoea", "syndromes", "blood", "local", "next", "watery", "nausea", "vomiting", "atrial", "fibrillation" ]
[ { "code": "ME05.1", "title": "Diarrhoea" }, { "code": "1A40.Z", "title": "Infectious gastroenteritis or colitis without specification of infectious agent" }, { "code": "DA90.0", "title": "Syndromic diarrhoea" }, { "code": "DD91.2", "title": "Functional diarrhoea" }, { "code": "1A2Z", "title": "Viral intestinal infections, unspecified" }, { "code": "1D9Z", "title": "Unspecified viral infection of unspecified site" }, { "code": "LD27.0Y", "title": "Other specified ectodermal dysplasia syndromes" }, { "code": "5A44", "title": "Insulin-resistance syndromes" }, { "code": "LD24.04", "title": "Chondrodysplasia punctata" }, { "code": "3C0Z", "title": "Diseases of the blood or blood-forming organs, unspecified" } ]
=== ICD-11 CODES FOUND === [ME05.1] Diarrhoea Definition: Diarrhoea is an acute or chronic condition in which there is an increased frequency or decreased consistency of bowel movements, usually with excessive and frequent evacuation of watery faeces. Here diarrhoea other than specifically described elsewhere, such as in motility disorders of intestine or in functional bowel diseases, is described. Also known as: Diarrhoea | noninfectious diarrhoea | frequent/loose bowel movements | watery stools | catarrhal diarrhoea Includes: frequent/loose bowel movements | watery stools Excludes: Melaena | Change in faeces or bowel movements | Functional diarrhoea [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] [DA90.0] Syndromic diarrhoea Definition: Syndromic diarrhoea (SD), also known as phenotypic diarrhoea (PD) or tricho-hepato-enteric syndrome (THE), is a congenital enteropathy presenting with early-onset of severe diarrhoea requiring parenteral nutrition (PN), associated with facial dysmorphism, woolly and poorly pigmented hair and liver disease, with extensive fibrosis or cirrhosis, in about half of the patients. Also known as: Syndromic diarrhoea | Phenotypic diarrhoea | THE - [tricho-hepato-enteric] syndrome Includes: Phenotypic diarrhoea [DD91.2] Functional diarrhoea Definition: Functional diarrhoea is a continuous or recurrent syndrome characterised by the passage of loose (mushy) or watery stools without abdominal pain or discomfort. Also known as: Functional diarrhoea [1A2Z] Viral intestinal infections, unspecified Also known as: Viral intestinal infections, unspecified | viral and other specified intestinal infections | acute infectious viral gastroenteritis | infantile gastroenteritis virus | infantile viral gastroenteritis [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 [LD27.0Y] Other specified ectodermal dysplasia syndromes Also known as: Other specified ectodermal dysplasia syndromes | Absence of fingerprints-congenital milia syndrome | Ackerman syndrome | ADULT syndrome | Acro-dermato-ungual-lacrimal-tooth syndrome [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 [LD24.04] Chondrodysplasia punctata Also known as: Chondrodysplasia punctata | chondrodysplasia punctata (stippled epiphyses) group | chondrodysplasia punctata congenita | dysplasia punctata epiphysis | dysplasia punctata [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 === GRAPH WALKS === --- Walk 1 --- [ME05.1] Diarrhoea Def: Diarrhoea is an acute or chronic condition in which there is an increased frequency or decreased consistency of bowel movements, usually with excessive and frequent evacuation of watery faeces. Here d... --EXCLUDES--> [?] Melaena Def: It is bloody stools that indicate bleeding from vascular system in the digestive tract. It is also described as black, tarry, and foul-smelling stools or red/maroon-coloured stools that contain degrad... --PARENT--> [?] Symptoms related to the lower gastrointestinal tract or abdomen --- Walk 2 --- [ME05.1] Diarrhoea Def: Diarrhoea is an acute or chronic condition in which there is an increased frequency or decreased consistency of bowel movements, usually with excessive and frequent evacuation of watery faeces. Here d... --EXCLUDES--> [?] Change in faeces or bowel movements --PARENT--> [?] Symptoms related to the lower gastrointestinal tract or abdomen --- Walk 3 --- [1A40.Z] Infectious gastroenteritis or colitis without specification of infectious agent --PARENT--> [1A40] Gastroenteritis or colitis without specification of infectious agent --EXCLUDES--> [?] Noninfectious neonatal diarrhoea Def: Non-infectious causes of diarrhoea in neonates. Childhood diarrhoea is most often caused by infection. Much less often, however, it is due to other causes - e.g., malabsorption or dietary intolerance,... --- Walk 4 --- [1A40.Z] Infectious gastroenteritis or colitis without specification of infectious agent --PARENT--> [1A40] Gastroenteritis or colitis without specification of infectious agent --EXCLUDES--> [?] Diarrhoea Def: Diarrhoea is an acute or chronic condition in which there is an increased frequency or decreased consistency of bowel movements, usually with excessive and frequent evacuation of watery faeces. Here d... --- Walk 5 --- [DA90.0] Syndromic diarrhoea Def: Syndromic diarrhoea (SD), also known as phenotypic diarrhoea (PD) or tricho-hepato-enteric syndrome (THE), is a congenital enteropathy presenting with early-onset of severe diarrhoea requiring parente... --PARENT--> [DA90] Nonstructural developmental anomalies of small intestine Def: Any congenital defect of small intestine that results from interference with the normal growth and differentiation of the fetus. Such defects can arise at any stage of embryonic development, vary grea... --RELATED_TO--> [?] Maltase-glucoamylase deficiency Def: Chronic diarrhea due to glucoamylase deficiency is characterised by chronic diarrhoea in infancy or childhood in association with intestinal glucoamylase deficiency.... --- Walk 6 --- [DA90.0] Syndromic diarrhoea Def: Syndromic diarrhoea (SD), also known as phenotypic diarrhoea (PD) or tricho-hepato-enteric syndrome (THE), is a congenital enteropathy presenting with early-onset of severe diarrhoea requiring parente... --PARENT--> [DA90] Nonstructural developmental anomalies of small intestine Def: Any congenital defect of small intestine that results from interference with the normal growth and differentiation of the fetus. Such defects can arise at any stage of embryonic development, vary grea... --CHILD--> [DA90.0] Syndromic diarrhoea Def: Syndromic diarrhoea (SD), also known as phenotypic diarrhoea (PD) or tricho-hepato-enteric syndrome (THE), is a congenital enteropathy presenting with early-onset of severe diarrhoea requiring parente...
[ "[ME05.1] Diarrhoea\n Def: Diarrhoea is an acute or chronic condition in which there is an increased frequency or decreased consistency of bowel movements, usually with excessive and frequent evacuation of watery faeces. Here d...\n --EXCLUDES--> [?] Melaena\n Def: It is bloody stools that indicate bleeding from vascular system in the digestive tract. It is also described as black, tarry, and foul-smelling stools or red/maroon-coloured stools that contain degrad...\n --PARENT--> [?] Symptoms related to the lower gastrointestinal tract or abdomen", "[ME05.1] Diarrhoea\n Def: Diarrhoea is an acute or chronic condition in which there is an increased frequency or decreased consistency of bowel movements, usually with excessive and frequent evacuation of watery faeces. Here d...\n --EXCLUDES--> [?] Change in faeces or bowel movements\n --PARENT--> [?] Symptoms related to the lower gastrointestinal tract or abdomen", "[1A40.Z] Infectious gastroenteritis or colitis without specification of infectious agent\n --PARENT--> [1A40] Gastroenteritis or colitis without specification of infectious agent\n --EXCLUDES--> [?] Noninfectious neonatal diarrhoea\n Def: Non-infectious causes of diarrhoea in neonates. Childhood diarrhoea is most often caused by infection. Much less often, however, it is due to other causes - e.g., malabsorption or dietary intolerance,...", "[1A40.Z] Infectious gastroenteritis or colitis without specification of infectious agent\n --PARENT--> [1A40] Gastroenteritis or colitis without specification of infectious agent\n --EXCLUDES--> [?] Diarrhoea\n Def: Diarrhoea is an acute or chronic condition in which there is an increased frequency or decreased consistency of bowel movements, usually with excessive and frequent evacuation of watery faeces. Here d...", "[DA90.0] Syndromic diarrhoea\n Def: Syndromic diarrhoea (SD), also known as phenotypic diarrhoea (PD) or tricho-hepato-enteric syndrome (THE), is a congenital enteropathy presenting with early-onset of severe diarrhoea requiring parente...\n --PARENT--> [DA90] Nonstructural developmental anomalies of small intestine\n Def: Any congenital defect of small intestine that results from interference with the normal growth and differentiation of the fetus. Such defects can arise at any stage of embryonic development, vary grea...\n --RELATED_TO--> [?] Maltase-glucoamylase deficiency\n Def: Chronic diarrhea due to glucoamylase deficiency is characterised by chronic diarrhoea in infancy or childhood in association with intestinal glucoamylase deficiency....", "[DA90.0] Syndromic diarrhoea\n Def: Syndromic diarrhoea (SD), also known as phenotypic diarrhoea (PD) or tricho-hepato-enteric syndrome (THE), is a congenital enteropathy presenting with early-onset of severe diarrhoea requiring parente...\n --PARENT--> [DA90] Nonstructural developmental anomalies of small intestine\n Def: Any congenital defect of small intestine that results from interference with the normal growth and differentiation of the fetus. Such defects can arise at any stage of embryonic development, vary grea...\n --CHILD--> [DA90.0] Syndromic diarrhoea\n Def: Syndromic diarrhoea (SD), also known as phenotypic diarrhoea (PD) or tricho-hepato-enteric syndrome (THE), is a congenital enteropathy presenting with early-onset of severe diarrhoea requiring parente..." ]
ME05.1
Diarrhoea
[ { "from_icd11": "ME05.1", "icd10_code": "R197", "icd10_title": "Diarrhea, unspecified" }, { "from_icd11": "1A40.Z", "icd10_code": "A09", "icd10_title": "Infectious gastroenteritis and colitis, unspecified" }, { "from_icd11": "1A40.Z", "icd10_code": "A00-A09", "icd10_title": "" }, { "from_icd11": "1A40.Z", "icd10_code": "A090", "icd10_title": "" }, { "from_icd11": "DA90.0", "icd10_code": "K529", "icd10_title": "Noninfective gastroenteritis and colitis, unspecified" }, { "from_icd11": "DD91.2", "icd10_code": "K591", "icd10_title": "Functional diarrhea" }, { "from_icd11": "1A2Z", "icd10_code": "A088", "icd10_title": "Other specified intestinal infections" }, { "from_icd11": "1A2Z", "icd10_code": "A0839", "icd10_title": "Other viral enteritis" }, { "from_icd11": "1A2Z", "icd10_code": "A084", "icd10_title": "Viral intestinal infection, unspecified" }, { "from_icd11": "1A2Z", "icd10_code": "A08", "icd10_title": "Viral and other specified intestinal infections" }, { "from_icd11": "1A2Z", "icd10_code": "A083", "icd10_title": "Other viral enteritis" }, { "from_icd11": "1D9Z", "icd10_code": "B348", "icd10_title": "Other viral infections of unspecified site" }, { "from_icd11": "1D9Z", "icd10_code": "B349", "icd10_title": "Viral infection, unspecified" }, { "from_icd11": "1D9Z", "icd10_code": "B344", "icd10_title": "Papovavirus infection, unspecified" }, { "from_icd11": "1D9Z", "icd10_code": "B333", "icd10_title": "Retrovirus infections, not elsewhere classified" } ]
R197
Diarrhea, unspecified
A 76‐year‐old man visited a private hospital with a chief complaint of left lower limb pain. Computed tomography and MRI revealed an irregular enlarged prostate in the left lobe, left obturator lymph node involvement, and multiple bone metastases . Bone scintigraphy confirmed the multiple bone metastases . A transrectal prostate biopsy was performed, as his serum PSA level was 365.156 ng/mL (normal range: <4.0 ng/mL). Histological evaluation led to the initial diagnosis of adenocarcinoma of Gleason score 4 + 4 and clinical stage T3a N1 M1b. ADT was performed immediately. The nadir PSA level was 0.213 ng/mL 13 months after ADT, the obturator lymph node was unclear but gradually increased. He developed CRPC 6 months after the initial treatment. Therefore, he received enzalutamide 160 mg/day and attained a serum PSA level of 0.002 ng/mL 7 months after the second treatment. The prostate volume was clearly decreased on MRI . The multiple bone metastases had disappeared on bone scintigraphy . As we deemed the patients’ mCRPC to be curable with immediate surgery, we performed RARP without PLND 1 year after diagnosis. The console time was 54 min, and the estimated blood loss was 10 mL. No surgery‐related adverse events occurred. Histopathological examination revealed that PCa cells disappeared into the prostate, and he attained pCR . He maintained an undetectable serum PSA level 6 months after surgery.
3.925781
0.978027
sec[1]/p[0]
en
0.999996
33426491
https://doi.org/10.1002/iju5.12229
[ "bone", "prostate", "multiple", "metastases", "serum", "obturator", "lymph", "node", "scintigraphy", "attained" ]
[ { "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": "GA90", "title": "Hyperplasia of prostate" }, { "code": "GA91.Z", "title": "Inflammatory or other diseases of prostate, unspecified" }, { "code": "GA91.Y", "title": "Other specified inflammatory or other diseases of prostate" }, { "code": "GA91.0", "title": "Chronic prostatitis" }, { "code": "MF40.1", "title": "Problems of the prostate" } ]
=== ICD-11 CODES FOUND === [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 [GA90] Hyperplasia of prostate Definition: A condition of the prostate, caused by an increased rate of cellular division of the glandular and stromal cells. This condition is characterised by enlargement of the prostatic tissue, dysuria, urinary urgency, nocturia, weak urine stream, straining while urinating, incomplete bladder emptying during urination, or increased frequency of urinary tract infection. Also known as: Hyperplasia of prostate | Adenofibromatous hypertrophy of prostate | benign prostatic hyperplasia | prostate hyperplasia | prostatic area hypertrophy Includes: Adenofibromatous hypertrophy of prostate Excludes: Benign neoplasms of prostate [GA91.Z] Inflammatory or other diseases of prostate, unspecified Also known as: Inflammatory or other diseases of prostate, unspecified | Inflammatory or other diseases of prostate | inflammation of prostate NOS | prostatitis NOS | disease of prostate NOS [GA91.Y] Other specified inflammatory or other diseases of prostate Also known as: Other specified inflammatory or other diseases of prostate | Acute bacterial prostatitis | acute prostatitis | Prostatitis category I (NIH classification) | Prostatitis category I [GA91.0] Chronic prostatitis Definition: A condition caused by obstruction of the prostate glands. This condition is characterised by inflammation of the prostate gland, dysuria, pollakiuria, urinary urgency, genital pain, lower back pain, abdominal pain, and repeated bladder infections that last for at least three months. Also known as: Chronic prostatitis | Fibrous prostatitis | Hypertrophic prostatitis | Subacute prostatitis | Chronic bacterial prostatitis [MF40.1] Problems of the prostate Definition: A group of disorders associated with the prostate occurring in diseases more specifically classified elsewhere. Also known as: Problems of the prostate === GRAPH WALKS === --- Walk 1 --- [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.... --CHILD--> [?] Conditions associated with the spine Def: This is a group of conditions in which there is a deviation from or interruption of the normal structure or function of the spine.... --- Walk 3 --- [FB84.Z] Osteomyelitis or osteitis, unspecified --PARENT--> [FB84] Osteomyelitis or osteitis --EXCLUDES--> [?] Infection of vertebra Def: A condition of the vertebrae, caused by an infection with a bacterial, viral, fungal, or parasitic source. This condition commonly presents with fever, chills, headache, weight loss, or may be asympto... --- Walk 4 --- [FB84.Z] Osteomyelitis or osteitis, unspecified --PARENT--> [FB84] Osteomyelitis or osteitis --CHILD--> [FB84.1] Other acute osteomyelitis --- Walk 5 --- [FB80.Z] Disorder of bone density or structure, unspecified --PARENT--> [FB80] Certain specified disorders of bone density or structure --CHILD--> [FB80.0] Fibrous dysplasia of bone Def: Fibrous dysplasia of bone is a congenital non-hereditary benign bone disease, where normal bone is replaced by a fibrous-like tissue with immature osteogenesis. Bone lesions are mono- or polyostotic a... --- Walk 6 --- [FB80.Z] Disorder of bone density or structure, unspecified --PARENT--> [FB80] Certain specified disorders of bone density or structure --EXCLUDES--> [?] Osteopoikilosis
[ "[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 --CHILD--> [?] Conditions associated with the spine\n Def: This is a group of conditions in which there is a deviation from or interruption of the normal structure or function of the spine....", "[FB84.Z] Osteomyelitis or osteitis, unspecified\n --PARENT--> [FB84] Osteomyelitis or osteitis\n --EXCLUDES--> [?] Infection of vertebra\n Def: A condition of the vertebrae, caused by an infection with a bacterial, viral, fungal, or parasitic source. This condition commonly presents with fever, chills, headache, weight loss, or may be asympto...", "[FB84.Z] Osteomyelitis or osteitis, unspecified\n --PARENT--> [FB84] Osteomyelitis or osteitis\n --CHILD--> [FB84.1] Other acute osteomyelitis", "[FB80.Z] Disorder of bone density or structure, unspecified\n --PARENT--> [FB80] Certain specified disorders of bone density or structure\n --CHILD--> [FB80.0] Fibrous dysplasia of bone\n Def: Fibrous dysplasia of bone is a congenital non-hereditary benign bone disease, where normal bone is replaced by a fibrous-like tissue with immature osteogenesis. Bone lesions are mono- or polyostotic a...", "[FB80.Z] Disorder of bone density or structure, unspecified\n --PARENT--> [FB80] Certain specified disorders of bone density or structure\n --EXCLUDES--> [?] Osteopoikilosis" ]
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
Patient 2 was a 73-year-old right-handed woman with a 5-year history of progressive decline in verbal communication, characterized by sparse and slow speech production. She did not speak unless addressed but produced stereotyped phrases, generated lengthy monologs, while echoing most of what she heard and completing simple open-ended sentences. It was also noticed that her regional accent was reverted to a previous variant learned during childhood . Her auditory comprehension and naming abilities were mildly impaired, but repetition was virtually intact. Two years after showing first deficits in spoken speech production, she suffered four falls in 1 year and developed apathy, bradyphrenia and emotional incontinence displaying uncontrollable episodes of crying and laughing. Neurological examination disclosed slow, hypometric saccades, decreased rate blink, bilateral limb rigidity with impaired finger and toe tapping, as well as tremor and bilateral hand grasping. She also showed neck rigidity, wide-based gait, postural instability, and problems arising from a chair and shortcomings on sitting down. Features consistent with PSP were revealed with the PSPRS . Family history was negative for movement disorders or dementia. A brain MRI showed moderate cortical, subcortical, and midbrain tegmentum atrophy . Treatments with carbidopa/levodopa (25/250 mg/tid) and amantadine (300 mg/bid) were unhelpful.
4.042969
0.980469
sec[1]/p[2]
en
0.999998
34017242
https://doi.org/10.3389/fnagi.2021.635896
[ "slow", "speech", "production", "impaired", "rigidity", "handed", "decline", "verbal", "communication", "characterized" ]
[ { "code": "MB23.N", "title": "Psychomotor retardation" }, { "code": "9C85.00", "title": "Disorders of the saccadic pulse" }, { "code": "KA20.1Z", "title": "Intrauterine growth restriction, unspecified" }, { "code": "8E0Y", "title": "Other specified human prion diseases" }, { "code": "8C61", "title": "Congenital myasthenic syndromes" }, { "code": "MA80.Z", "title": "Speech or language disturbances, unspecified" }, { "code": "MB23.L", "title": "Pressured speech" }, { "code": "6B60.5", "title": "Dissociative neurological symptom disorder, with speech disturbance" }, { "code": "MB25.02", "title": "Disorganised thinking" }, { "code": "MA81", "title": "Speech dysfluency" } ]
=== ICD-11 CODES FOUND === [MB23.N] Psychomotor retardation Definition: A visible generalised slowing of movements and speech. Also known as: Psychomotor retardation | slowness and poor responsiveness | slow behaviour | poor responsiveness behaviour Excludes: Stupor [9C85.00] Disorders of the saccadic pulse Also known as: Disorders of the saccadic pulse | Disorders of saccadic velocity | Slow saccades | Disorders of saccadic accuracy | Saccadic (pulse) dysmetria [KA20.1Z] Intrauterine growth restriction, unspecified Also known as: Intrauterine growth restriction, unspecified | Intrauterine growth restriction | IUGR - [Intrauterine growth restriction] | fetal growth retardation, unspecified weight | FGR - [fetal growth retardation] [8E0Y] Other specified human prion diseases Also known as: Other specified human prion diseases | Slow virus infection [8C61] Congenital myasthenic syndromes Definition: Congenital myasthenic syndrome (CMS) is a heterogeneous group of genetically determined diseases. There are four well-defined categories: Congenital myasthenic syndrome with presynaptic defect, Synaptic basal lamina-associated CMS, Congenital myasthenia with postsynaptic defect, CMS with glycosylation deficiency, and the remaining category is that of unidentified CMS. Also known as: Congenital myasthenic syndromes | congenital and developmental myasthenia | developmental myasthenia | congenital myasthenia | Congenital endplate acetylcholine receptor deficiency [MA80.Z] Speech or language disturbances, unspecified Also known as: Speech or language disturbances, unspecified | Speech or language disturbances | speech defect NOS | speech disorder NOS | problem with voice production [MB23.L] Pressured speech Definition: Speech in which the person feels undue pressure to get the words out. The person’s speech is usually rapid, loud, and emphatic and may be difficult or impossible to interrupt. Frequently, the person talks without any social stimulation and may continue to talk even though no one is listening. Also known as: Pressured speech Excludes: Schizophrenia or other primary psychotic disorders | Bipolar or related disorders [6B60.5] Dissociative neurological symptom disorder, with speech disturbance Definition: Dissociative neurological symptom disorder, with speech disturbance is characterised by symptoms such as difficulty with speaking (dysphonia), loss of the ability to speak (aphonia) or difficult or unclear articulation of speech (dysarthria) that are not consistent with a recognised disease of the nervous system, a neurodevelopmental or neurocognitive disorder, other mental, behavioural or neurodevelopmental disorder, or other medical condition and do not occur exclusively during another dissoci Also known as: Dissociative neurological symptom disorder, with speech disturbance | Functional neurological symptom disorder, with speech disturbance | Functional speech disorder [MB25.02] Disorganised thinking Definition: A disturbance in the associative thought process typically manifested in speech in which the person shifts suddenly from one topic to another that is unrelated or minimally related to the first. The individual gives no indication of being aware of the disconnectedness or illogicality of their thinking. Also known as: Disorganised thinking | thought derailment | loose associations | disorganised speech [MA81] Speech dysfluency Definition: Speech dysfluency is characterised by the frequent or pervasive disruption of the rhythmic flow of speech that arises subsequent to the developmental period (i.e., adult onset) and is outside the limits of normal variation and results in reduced intelligibility and significantly affects communication. It can involve repetitions of sounds, syllables or words, prolongations, word breaks, blockage of production, excessive use of interjections, and rapid short bursts of speech. Also known as: Speech dysfluency | speech impediment NOS | Adult onset cluttering | Adult onset stammering | Adult onset stuttering Excludes: Developmental language disorder | Developmental speech or language disorders | Developmental speech fluency disorder === GRAPH WALKS === --- Walk 1 --- [MB23.N] Psychomotor retardation Def: A visible generalised slowing of movements and speech.... --PARENT--> [MB23] Symptoms or signs involving appearance or behaviour --CHILD--> [MB23.2] Avoidance behaviour Def: The act of keeping away from circumstances, situations, or stimuli that cause anxiety or other negative emotions in the individual.... --- Walk 2 --- [MB23.N] Psychomotor retardation Def: A visible generalised slowing of movements and speech.... --EXCLUDES--> [?] Stupor Def: Total or nearly total lack of spontaneous movement and marked decrease in reactivity to environment.... --EXCLUDES--> [?] 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 ... --- Walk 3 --- [9C85.00] Disorders of the saccadic pulse --PARENT--> [9C85.0] Anomalies of saccadic eye movements --PARENT--> [9C85] Certain specified irregular eye movements --- Walk 4 --- [9C85.00] Disorders of the saccadic pulse --PARENT--> [9C85.0] Anomalies of saccadic eye movements --CHILD--> [9C85.02] Inappropriate saccades --- Walk 5 --- [KA20.1Z] Intrauterine growth restriction, unspecified --PARENT--> [KA20.1] Intrauterine growth restriction Def: The fetus does not achieve its predicted genetic potential and infant, not light or small for gestational age, showing signs of fetal malnutrition.... --CHILD--> [KA20.11] Symmetrical intrauterine growth restriction Def: This condition begins earlier in pregnancy and there is a higher incidence of permanent neurologic sequela. It is often associated with either genetic abnormalities or fetal infection, especially 1st ... --- Walk 6 --- [KA20.1Z] Intrauterine growth restriction, unspecified --PARENT--> [KA20.1] Intrauterine growth restriction Def: The fetus does not achieve its predicted genetic potential and infant, not light or small for gestational age, showing signs of fetal malnutrition.... --CHILD--> [KA20.11] Symmetrical intrauterine growth restriction Def: This condition begins earlier in pregnancy and there is a higher incidence of permanent neurologic sequela. It is often associated with either genetic abnormalities or fetal infection, especially 1st ...
[ "[MB23.N] Psychomotor retardation\n Def: A visible generalised slowing of movements and speech....\n --PARENT--> [MB23] Symptoms or signs involving appearance or behaviour\n --CHILD--> [MB23.2] Avoidance behaviour\n Def: The act of keeping away from circumstances, situations, or stimuli that cause anxiety or other negative emotions in the individual....", "[MB23.N] Psychomotor retardation\n Def: A visible generalised slowing of movements and speech....\n --EXCLUDES--> [?] Stupor\n Def: Total or nearly total lack of spontaneous movement and marked decrease in reactivity to environment....\n --EXCLUDES--> [?] 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 ...", "[9C85.00] Disorders of the saccadic pulse\n --PARENT--> [9C85.0] Anomalies of saccadic eye movements\n --PARENT--> [9C85] Certain specified irregular eye movements", "[9C85.00] Disorders of the saccadic pulse\n --PARENT--> [9C85.0] Anomalies of saccadic eye movements\n --CHILD--> [9C85.02] Inappropriate saccades", "[KA20.1Z] Intrauterine growth restriction, unspecified\n --PARENT--> [KA20.1] Intrauterine growth restriction\n Def: The fetus does not achieve its predicted genetic potential and infant, not light or small for gestational age, showing signs of fetal malnutrition....\n --CHILD--> [KA20.11] Symmetrical intrauterine growth restriction\n Def: This condition begins earlier in pregnancy and there is a higher incidence of permanent neurologic sequela. It is often associated with either genetic abnormalities or fetal infection, especially 1st ...", "[KA20.1Z] Intrauterine growth restriction, unspecified\n --PARENT--> [KA20.1] Intrauterine growth restriction\n Def: The fetus does not achieve its predicted genetic potential and infant, not light or small for gestational age, showing signs of fetal malnutrition....\n --CHILD--> [KA20.11] Symmetrical intrauterine growth restriction\n Def: This condition begins earlier in pregnancy and there is a higher incidence of permanent neurologic sequela. It is often associated with either genetic abnormalities or fetal infection, especially 1st ..." ]
MB23.N
Psychomotor retardation
[ { "from_icd11": "MB23.N", "icd10_code": "R464", "icd10_title": "Slowness and poor responsiveness" }, { "from_icd11": "9C85.00", "icd10_code": "H49-H52", "icd10_title": "" }, { "from_icd11": "8C61", "icd10_code": "G702", "icd10_title": "Congenital and developmental myasthenia" }, { "from_icd11": "MA80.Z", "icd10_code": "R479", "icd10_title": "Unspecified speech disturbances" }, { "from_icd11": "MA80.Z", "icd10_code": "R4702", "icd10_title": "Dysphasia" }, { "from_icd11": "MA80.Z", "icd10_code": "R4789", "icd10_title": "Other speech disturbances" }, { "from_icd11": "MA80.Z", "icd10_code": "R4781", "icd10_title": "Slurred speech" }, { "from_icd11": "MA80.Z", "icd10_code": "R4782", "icd10_title": "Fluency disorder in conditions classified elsewhere" }, { "from_icd11": "MA80.Z", "icd10_code": "R47", "icd10_title": "Speech disturbances, not elsewhere classified" }, { "from_icd11": "MA80.Z", "icd10_code": "R470", "icd10_title": "Dysphasia and aphasia" }, { "from_icd11": "MA80.Z", "icd10_code": "R478", "icd10_title": "Other speech disturbances" }, { "from_icd11": "MB25.02", "icd10_code": "R4689", "icd10_title": "Other symptoms and signs involving appearance and behavior" }, { "from_icd11": "MB25.02", "icd10_code": "R4681", "icd10_title": "Obsessive-compulsive behavior" }, { "from_icd11": "MB25.02", "icd10_code": "R468", "icd10_title": "Other symptoms and signs involving appearance and behavior" } ]
R464
Slowness and poor responsiveness
Histologically, the tumor was an invasive ductal carcinoma with 4.8 × 2.0 cm in size. Several intraductal components and lymphatic invasion were observed. The stage was determined to be pT2N1M0 (stage IIB). Immunohistochemical examination revealed that the tumor was ER-positive, PgR-negative, and HER2-positive, with a Ki-67 index of 20% . Although bilateral breast cancer subtypes were similar, eventually, we judged the left breast cancer to be a second primary lesion as the reason for existence because of the intraductal components . Postoperatively, chemotherapy and targeted therapy (docetaxel, trastuzumab, and pertuzumab) and endocrine therapy (toremifene and leuprorelin) were administered. Fig. 2 Histopathological findings of bilateral breast cancers. The right breast cancer is shown in a – e , and the left breast cancer is shown in f – j : hematoxylin-eosin staining ( a , f ), ER ( b , g ), PgR ( c , h ), HER2 ( d , i ), and Ki-67 ( e , j ). Immunohistochemical staining results were ER, 5; PgR, 4; HER2, 2+; and Ki-67, 35.6% for the right lesion, and ER, 5; PgR, 1; HER2, 2+; and Ki-67, 20% for the left lesion Fig. 3 Macroscopic distribution of cancer in the left breast. A few intraductal components were present (dotted red line) in part of the invasive area (red line) Fig. 4 Intraductal metastatic carcinoma lesion in the left breast. Hematoxylin-eosin staining ( a ), ER ( b ), and CD10 ( c )
4.003906
0.886719
sec[1]/p[1]
en
0.999998
32833091
https://doi.org/10.1186/s40792-020-00966-y
[ "breast", "cancer", "intraductal", "lesion", "components", "staining", "tumor", "invasive", "carcinoma", "stage" ]
[ { "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": "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 === [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 [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 --- [GB23] Certain specified disorders of breast Def: Any disorder of the breast or breast tissue, characterised by pathological changes, not classified elsewhere.... --CHILD--> [GB23.2] Fat necrosis of breast Def: A condition of the breast, caused by saponification of fat tissue, commonly subsequent to trauma or radiation therapy. This condition is characterised by damage, death, or inflammation of the fat tiss... --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.... --RELATED_TO--> [?] Other signs or symptoms in breast Def: Any sign or symptom of the breast, not classified elsewhere.... --PARENT--> [?] Certain specified disorders of breast Def: Any disorder of the breast or breast tissue, characterised by pathological changes, not classified elsewhere.... --- 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.... --RELATED_TO--> [?] Neonatal infectious mastitis Def: A disease of the breasts in neonates, may be caused by a maternal infection with a bacterial source. This disease is characterised by swelling, erythema, warmth, tenderness, induration of the breast, ... --- 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--> [GB23.2] Fat necrosis of breast\n Def: A condition of the breast, caused by saponification of fat tissue, commonly subsequent to trauma or radiation therapy. This condition is characterised by damage, death, or inflammation of the fat tiss...\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 --RELATED_TO--> [?] Other signs or symptoms in breast\n Def: Any sign or symptom of the breast, not classified elsewhere....\n --PARENT--> [?] Certain specified disorders of breast\n Def: Any disorder of the breast or breast tissue, characterised by pathological changes, not classified elsewhere....", "[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 --RELATED_TO--> [?] Neonatal infectious mastitis\n Def: A disease of the breasts in neonates, may be caused by a maternal infection with a bacterial source. This disease is characterised by swelling, erythema, warmth, tenderness, induration of the 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 --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
A 36-year-old woman initially went to a neurologist with complaints of frequent soreness in her right leg, and pain in the right instep, suspected to be a pinched nerve from the spine. Then, the longer the feeling of a lump in the right popliteal fossa, the diagnosis was “Baker's cyst.” Since 5 years ago, the right knee has felt sore, and since 4 years ago, it felt like a lump was getting bigger. The right instep to the lateral side of the ankle and the 1/3 distal of the lower leg sometimes felt hot, like burning, or painful like pulling. Since 2 years ago, it sometimes feels like an electric shock from the fold of the right knee to the right instep along the lateral side of the lower leg if the lump in the right popliteal fossa is hit (Tinel's sign is positive). The lump gets bigger, hurts more often, and interferes with rest or sleep at night. A physical examination showed that the patient was in pain, and no abnormalities were found in the vertebrae or elsewhere. In the right popliteal fossa, a mass was palpable, deep, more lateral, spongy, flat, mobile, single, and tender, and Tinel's sign was positive. Hypoesthesia sensibility in the right instep to the lateral ankle and distal to the right lower leg, and a slight drop in the foot . On radiographic examination of the right knee, a circumscript, single, more lateral mass was seen, measuring approximately 4 cm × 5 cm in the popliteal fossa .
3.744141
0.986328
sec[1]/p[0]
en
0.999999
39262572
https://doi.org/10.1155/2024/9397436
[ "instep", "lump", "popliteal", "fossa", "like", "since", "knee", "felt", "pain", "bigger" ]
[ { "code": "ME61", "title": "Subcutaneous swelling, mass or lump of uncertain or unspecified nature" }, { "code": "MD82", "title": "Intra-abdominal or pelvic swelling, mass or lump" }, { "code": "LB30.61", "title": "Fused pelvic kidney" }, { "code": "MF30", "title": "Breast lump or mass female" }, { "code": "CA0H.2", "title": "Nodules of vocal cords" }, { "code": "LD26.4Y", "title": "Other specified arthrogryposis syndromes" }, { "code": "NC95.00", "title": "Laceration of popliteal artery" }, { "code": "BD30.20&XA44K1", "title": "Acute thromboembolic popliteal artery occlusion" }, { "code": "BD30.21&XA44K1", "title": "Acute thrombotic popliteal artery occlusion" }, { "code": "BD53.3", "title": "Popliteal entrapment syndrome" } ]
=== ICD-11 CODES FOUND === [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 [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 [LB30.61] Fused pelvic kidney Definition: A condition caused by failure of the kidneys to correctly develop during the antenatal period. This condition is characterised by the presence of a single kidney, along the midline of the body. This condition may present with kidney stones, hydronephrosis, kidney infection, haematuria, or may be asymptomatic. Confirmation is through observation of a fused kidney by imaging. Also known as: Fused pelvic kidney | Cake kidney | Pancake kidney | Lump kidney | Discoid kidney [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 [CA0H.2] Nodules of vocal cords Also known as: Nodules of vocal cords | chorditis cantorum | nodular chorditis | nodule of the vocal cord | screamer's node [LD26.4Y] Other specified arthrogryposis syndromes Also known as: Other specified arthrogryposis syndromes | Popliteal pterygium syndrome | Popliteal web syndrome | Bartsocas-Papas syndrome | Autosomal dominant popliteal pterygium syndrome [NC95.00] Laceration of popliteal artery Also known as: Laceration of popliteal artery [BD53.3] Popliteal entrapment syndrome Also known as: Popliteal entrapment syndrome | Popliteal artery entrapment syndrome === GRAPH WALKS === --- Walk 1 --- [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--> [?] Benign symmetrical lipomatosis Def: Benign symmetrical lipomatosis is an uncommon condition characterised by progressive symmetrical accumulation during adult life of adipose mass at the level of the head, neck and upper trunk . The con... --- Walk 2 --- [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 3 --- [MD82] Intra-abdominal or pelvic swelling, mass or lump Def: 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.... --EXCLUDES--> [?] Ascites Def: Accumulation or retention of free fluid in the abdominal peritoneal cavity between the tissues lining the abdomen and abdominal organs. The fluid may be serous, haemorrhagic, or the result of inflamma... --CHILD--> [?] Fluid in peritoneal cavity --- Walk 4 --- [MD82] Intra-abdominal or pelvic swelling, mass or lump Def: 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.... --EXCLUDES--> [?] Abdominal distension Def: This is a condition in which the abdomen feels full and tight because of swelling of the abdomen, usually due to an increased amount of intestinal gas, but occurs sometimes when fluid, substances or m... --PARENT--> [?] Symptoms related to the lower gastrointestinal tract or abdomen --- Walk 5 --- [LB30.61] Fused pelvic kidney Def: A condition caused by failure of the kidneys to correctly develop during the antenatal period. This condition is characterised by the presence of a single kidney, along the midline of the body. This c... --PARENT--> [LB30.6] Fusion anomaly of kidneys Def: The embryological, incomplete fusion of renal lobules and/or kidneys... --CHILD--> [LB30.60] Lobulated kidney Def: Any condition caused by incomplete fusion of the developing renal lobules during the antenatal period. This condition may be asymptomatic.... --- Walk 6 --- [LB30.61] Fused pelvic kidney Def: A condition caused by failure of the kidneys to correctly develop during the antenatal period. This condition is characterised by the presence of a single kidney, along the midline of the body. This c... --PARENT--> [LB30.6] Fusion anomaly of kidneys Def: The embryological, incomplete fusion of renal lobules and/or kidneys... --CHILD--> [LB30.61] Fused pelvic kidney Def: A condition caused by failure of the kidneys to correctly develop during the antenatal period. This condition is characterised by the presence of a single kidney, along the midline of the body. This c...
[ "[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--> [?] Benign symmetrical lipomatosis\n Def: Benign symmetrical lipomatosis is an uncommon condition characterised by progressive symmetrical accumulation during adult life of adipose mass at the level of the head, neck and upper trunk . The con...", "[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", "[MD82] Intra-abdominal or pelvic swelling, mass or lump\n Def: 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....\n --EXCLUDES--> [?] Ascites\n Def: Accumulation or retention of free fluid in the abdominal peritoneal cavity between the tissues lining the abdomen and abdominal organs. The fluid may be serous, haemorrhagic, or the result of inflamma...\n --CHILD--> [?] Fluid in peritoneal cavity", "[MD82] Intra-abdominal or pelvic swelling, mass or lump\n Def: 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....\n --EXCLUDES--> [?] Abdominal distension\n Def: This is a condition in which the abdomen feels full and tight because of swelling of the abdomen, usually due to an increased amount of intestinal gas, but occurs sometimes when fluid, substances or m...\n --PARENT--> [?] Symptoms related to the lower gastrointestinal tract or abdomen", "[LB30.61] Fused pelvic kidney\n Def: A condition caused by failure of the kidneys to correctly develop during the antenatal period. This condition is characterised by the presence of a single kidney, along the midline of the body. This c...\n --PARENT--> [LB30.6] Fusion anomaly of kidneys\n Def: The embryological, incomplete fusion of renal lobules and/or kidneys...\n --CHILD--> [LB30.60] Lobulated kidney\n Def: Any condition caused by incomplete fusion of the developing renal lobules during the antenatal period. This condition may be asymptomatic....", "[LB30.61] Fused pelvic kidney\n Def: A condition caused by failure of the kidneys to correctly develop during the antenatal period. This condition is characterised by the presence of a single kidney, along the midline of the body. This c...\n --PARENT--> [LB30.6] Fusion anomaly of kidneys\n Def: The embryological, incomplete fusion of renal lobules and/or kidneys...\n --CHILD--> [LB30.61] Fused pelvic kidney\n Def: A condition caused by failure of the kidneys to correctly develop during the antenatal period. This condition is characterised by the presence of a single kidney, along the midline of the body. This c..." ]
ME61
Subcutaneous swelling, mass or lump of uncertain or unspecified nature
[ { "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" }, { "from_icd11": "ME61", "icd10_code": "R221", "icd10_title": "Localized swelling, mass and lump, neck" }, { "from_icd11": "ME61", "icd10_code": "R222", "icd10_title": "Localized swelling, mass and lump, trunk" }, { "from_icd11": "ME61", "icd10_code": "R229", "icd10_title": "Localized swelling, mass and lump, unspecified" }, { "from_icd11": "ME61", "icd10_code": "R20-R23", "icd10_title": "" }, { "from_icd11": "ME61", "icd10_code": "R22", "icd10_title": "Localized swelling, mass and lump of skin and subcutaneous tissue" }, { "from_icd11": "ME61", "icd10_code": "R223", "icd10_title": "Localized swelling, mass and lump, upper limb" } ]
R2240
Localized swelling, mass and lump, unspecified lower limb
A 71-year-old healthy female visited to our emergency department because of upper back pain for 2 days, and she presented with fever. She was admitted for further evaluation and management. She denied any traumatic injury and acupuncture and invasive therapeutics. At admission Day, her vital sign showed a blood pressure of 140/90 mm Hg, body temperature 38.2°C, respiratory rate 26/min and heart beat 110/min. Physical examination and important clinical findings showed the painful sensation over middle part of T spine area and there were no significant neurological deficit. The initial laboratory data revealed white cell count, 9300/mm 3 ; ESR, 86 mm/h; CRP, 0.28 mg/L and PCT, 0.03 ng/mL. The MRI of the spine showed that abnormal signal intensity in the T8–9 vertebrae. The T8–9 VO was impressed. S aureus (2/2 sets) was identified by using matrix-assisted laser desorption ionization-time of flight mass spectrometry (bioMerieux, Hazlewood, Mo.) on 3 th admission day, and it was oxacillin susceptible strain according to the susceptibility test. Oxacillin susceptible S. aureus VO was suspected, and parenteral oxacillin 2000 mg every 4 hours was prescribed. She received the 42-days combination regimens without adverse and unanticipated events. The serial follow-up laboratory data normalized. She was discharged on 44 th admission days and was follow-up at outpatient department where she recovered well.
3.820313
0.98291
sec[1]/sec[1]/p[0]
en
0.999996
33120821
https://doi.org/10.1097/MD.0000000000022852
[ "oxacillin", "department", "spine", "laboratory", "data", "aureus", "susceptible", "healthy", "visited", "emergency" ]
[ { "code": "MG51.10", "title": "Penicillin resistant Streptococcus pneumoniae" }, { "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": "QA00.C", "title": "Laboratory examination" }, { "code": "MG71.Z", "title": "Abnormal laboratory results, not elsewhere classified, unspecified" }, { "code": "MG71.Y", "title": "Other specified abnormal laboratory results, not elsewhere classified" }, { "code": "QA0B", "title": "Preprocedural examination" } ]
=== ICD-11 CODES FOUND === [MG51.10] Penicillin resistant Streptococcus pneumoniae Also known as: Penicillin resistant Streptococcus pneumoniae | Oxacillin resistant Streptococcus pneumoniae | Penicillin G resistant Streptococcus pneumoniae [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 [QA00.C] Laboratory examination Also known as: Laboratory examination | laboratory test [MG71.Z] Abnormal laboratory results, not elsewhere classified, unspecified Also known as: Abnormal laboratory results, not elsewhere classified, unspecified | Abnormal laboratory results, not elsewhere classified [MG71.Y] Other specified abnormal laboratory results, not elsewhere classified Also known as: Other specified abnormal laboratory results, not elsewhere classified [QA0B] Preprocedural examination Definition: Evaluation and testing for assessment and proactive management of risks of perioperative morbidity and mortality and implements measurements to minimize risks. Also known as: Preprocedural examination | Encounter for preoperative examinations | Preprocedural general examination | Encounter for preprocedural examination NOS | preoperative assessment === GRAPH WALKS === --- Walk 1 --- [MG51.10] Penicillin resistant Streptococcus pneumoniae --PARENT--> [MG51.1] Antibiotic resistant Streptococcus pneumoniae --CHILD--> [MG51.12] Third-generation cephalosporins resistant Streptococcus pneumoniae --- Walk 2 --- [MG51.10] Penicillin resistant Streptococcus pneumoniae --PARENT--> [MG51.1] Antibiotic resistant Streptococcus pneumoniae --CHILD--> [MG51.10] Penicillin resistant Streptococcus pneumoniae --- Walk 3 --- [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 4 --- [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--> [?] Degenerative condition of spine Def: This is a disease characterised by degenerative changes in the intervertebral disc, vertebral end-plates and spinal joints due to aging or structural change.... --- Walk 5 --- [FA7Z] Structural disorders of spine, unspecified --PARENT--> [?] Structural disorders of spine --CHILD--> [FA70] Spinal deformities --- Walk 6 --- [FA7Z] Structural disorders of spine, unspecified --PARENT--> [?] Structural disorders 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....
[ "[MG51.10] Penicillin resistant Streptococcus pneumoniae\n --PARENT--> [MG51.1] Antibiotic resistant Streptococcus pneumoniae\n --CHILD--> [MG51.12] Third-generation cephalosporins resistant Streptococcus pneumoniae", "[MG51.10] Penicillin resistant Streptococcus pneumoniae\n --PARENT--> [MG51.1] Antibiotic resistant Streptococcus pneumoniae\n --CHILD--> [MG51.10] Penicillin resistant Streptococcus pneumoniae", "[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", "[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--> [?] Degenerative condition of spine\n Def: This is a disease characterised by degenerative changes in the intervertebral disc, vertebral end-plates and spinal joints due to aging or structural change....", "[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 --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...." ]
MG51.10
Penicillin resistant Streptococcus pneumoniae
[ { "from_icd11": "MG51.10", "icd10_code": "U820", "icd10_title": "" }, { "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" } ]
U820
Blood cultures obtained at the time of arrival to the ED returned positive for S. intermedius growth. All intraoperative samples also grew S. intermedius. One intraoperative sample revealed polymicrobial growth that included S. intermedius, Streptococcus salivarius, Rothia mucilaginosa, and Rothia dentocariosa. Surgical pathology of the C4 and C5 vertebral tissue culture grew S. intermedius. The cerebrospinal fluid analysis showed pleocytosis, elevated protein, and decreased glucose but no organism growth. The infectious disease department was consulted at this time for antibiotic recommendations. Due to the growth of the same organism from blood and operative cultures originating from a deep neck space infection complicated by cervical epidural abscess and osteomyelitis in the setting of an IJV thrombosis, a diagnosis of LS secondary to S. intermedius was made. Culture sensitivity results eventually showed sensitivity to ceftriaxone and penicillin after which cefepime was converted to high dose intravenous ceftriaxone two grams every 12 hours with metronidazole 500 milligrams three times daily continued for anaerobic coverage. The decision to administer high dose ceftriaxone was made considering the possibility of meningeal infection. Repeat blood cultures drawn 48 hours later were negative. Of note, two-dimensional transthoracic echocardiography showed no evidence of cardiac valve vegetation.
3.978516
0.967285
sec[1]/p[8]
en
0.999994
32455086
https://doi.org/10.7759/cureus.7787
[ "intermedius", "growth", "blood", "cultures", "ceftriaxone", "time", "intraoperative", "grew", "rothia", "culture" ]
[ { "code": "2F9Z", "title": "Neoplasms of unknown behaviour of unspecified site" }, { "code": "MG44.1Z", "title": "Lack of expected normal physiological development, unspecified" }, { "code": "5A61.3", "title": "Growth hormone deficiency" }, { "code": "8C7Y", "title": "Other specified primary disorders of muscles" }, { "code": "FB86.Z", "title": "Disorders associated with bone growth, 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 === [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 [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 [5A61.3] Growth hormone deficiency Definition: Deficiency of growth hormone in children, adolescents and adults. Includes deficiency of growth hormone releasing hormone (GHRH) and excess of central somatostatin, leading to growth hormone deficiency. Includes idiopathic, inborn and acquired forms of growth hormone deficiency. Also known as: Growth hormone deficiency Excludes: Hypopituitarism [8C7Y] Other specified primary disorders of muscles Also known as: Other specified primary disorders of muscles | Certain specified primary disorders of muscles | Myopathy due to calsequestrin or SERCA1 protein overload | Delayed muscle maturation | delayed muscle growth [FB86.Z] Disorders associated with bone growth, unspecified Also known as: Disorders associated with bone growth, unspecified | Disorders associated with bone growth [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 --- [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 --- [MG44.1Z] Lack of expected normal physiological development, unspecified --PARENT--> [MG44.1] Lack of expected normal physiological development Def: Lack of expected normal physiological development includes delayed milestone of development and other lack of expected normal physiological development including gross and fine motor development, lang... --CHILD--> [MG44.11] Failure to thrive in infant or child Def: When an infant or child's current weight or rate of weight gain is significantly below that of other children of similar age and gender.... --- Walk 4 --- [MG44.1Z] Lack of expected normal physiological development, unspecified --PARENT--> [MG44.1] Lack of expected normal physiological development Def: Lack of expected normal physiological development includes delayed milestone of development and other lack of expected normal physiological development including gross and fine motor development, lang... --CHILD--> [MG44.12] Short stature of child Def: Short stature is when a child is significantly shorter than children of the same age and gender... --- Walk 5 --- [5A61.3] Growth hormone deficiency Def: Deficiency of growth hormone in children, adolescents and adults. Includes deficiency of growth hormone releasing hormone (GHRH) and excess of central somatostatin, leading to growth hormone deficienc... --EXCLUDES--> [?] Hypopituitarism Def: A disorder manifesting a deficiency or decrease of one or more pituitary hormones, which is caused by a variety of diseases such as tumour, trauma/surgery, irradiation, inflammation and haemorrhage/in... --CHILD--> [?] Argonz-del Castillo Syndrome --- Walk 6 --- [5A61.3] Growth hormone deficiency Def: Deficiency of growth hormone in children, adolescents and adults. Includes deficiency of growth hormone releasing hormone (GHRH) and excess of central somatostatin, leading to growth hormone deficienc... --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--> [?] Postprocedural hypopituitarism Def: This is the postprocedural decreased (hypo) secretion of one or more of the eight hormones normally produced by the pituitary gland at the base of the brain. If there is decreased secretion of most pi...
[ "[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", "[MG44.1Z] Lack of expected normal physiological development, unspecified\n --PARENT--> [MG44.1] Lack of expected normal physiological development\n Def: Lack of expected normal physiological development includes delayed milestone of development and other lack of expected normal physiological development including gross and fine motor development, lang...\n --CHILD--> [MG44.11] Failure to thrive in infant or child\n Def: When an infant or child's current weight or rate of weight gain is significantly below that of other children of similar age and gender....", "[MG44.1Z] Lack of expected normal physiological development, unspecified\n --PARENT--> [MG44.1] Lack of expected normal physiological development\n Def: Lack of expected normal physiological development includes delayed milestone of development and other lack of expected normal physiological development including gross and fine motor development, lang...\n --CHILD--> [MG44.12] Short stature of child\n Def: Short stature is when a child is significantly shorter than children of the same age and gender...", "[5A61.3] Growth hormone deficiency\n Def: Deficiency of growth hormone in children, adolescents and adults. Includes deficiency of growth hormone releasing hormone (GHRH) and excess of central somatostatin, leading to growth hormone deficienc...\n --EXCLUDES--> [?] Hypopituitarism\n Def: A disorder manifesting a deficiency or decrease of one or more pituitary hormones, which is caused by a variety of diseases such as tumour, trauma/surgery, irradiation, inflammation and haemorrhage/in...\n --CHILD--> [?] Argonz-del Castillo Syndrome", "[5A61.3] Growth hormone deficiency\n Def: Deficiency of growth hormone in children, adolescents and adults. Includes deficiency of growth hormone releasing hormone (GHRH) and excess of central somatostatin, leading to growth hormone deficienc...\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--> [?] Postprocedural hypopituitarism\n Def: This is the postprocedural decreased (hypo) secretion of one or more of the eight hormones normally produced by the pituitary gland at the base of the brain. If there is decreased secretion of most pi..." ]
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": "MG44.1Z", "icd10_code": "R6250", "icd10_title": "Unspecified lack of expected normal physiological development in childhood" }, { "from_icd11": "MG44.1Z", "icd10_code": "R6259", "icd10_title": "Other lack of expected normal physiological development in childhood" }, { "from_icd11": "MG44.1Z", "icd10_code": "R6251", "icd10_title": "Failure to thrive (child)" }, { "from_icd11": "MG44.1Z", "icd10_code": "R6252", "icd10_title": "Short stature (child)" }, { "from_icd11": "MG44.1Z", "icd10_code": "R62", "icd10_title": "Lack of expected normal physiological development in childhood and adults" }, { "from_icd11": "MG44.1Z", "icd10_code": "R628", "icd10_title": "" }, { "from_icd11": "MG44.1Z", "icd10_code": "R629", "icd10_title": "" }, { "from_icd11": "FB86.Z", "icd10_code": "M89761", "icd10_title": "Major osseous defect, right lower leg" }, { "from_icd11": "FB86.Z", "icd10_code": "M89772", "icd10_title": "Major osseous defect, left ankle and foot" } ]
D487
Neoplasm of uncertain behavior of other specified sites
Case 4 (a bortezomib-based regimen intolerant case).The patient had a history of severe malabsorption syndrome, for which parenteral nutrition was started two years before. The patient presented with cachexia and depressive syndrome. Laboratory tests revealed nephrotic syndrome (proteinuria 8.2 g/24 h), Bence–Jones proteinuria associated with marked hypoprotidemia (serum albumin 1.2 g/dL and total serum proteins of 3.5 g/dL). She had an IgDλ M component with FLC λ 134 mg/L and FLC ratio 0.12. Tissue histological examination confirmed the clinical suspicion of amyloid deposits in the kidney, intestinal mucosa, and periombelical fat. Bone marrow showed a λ-restricted plasma cell clone (13%), and testing with Congo red staining was positive. No signs of cardiac or peripheral nervous system involvement were found. The patient was initially treated with bortezomib (1.3 mg/m 2 ), cyclophosphamide , and dexamethasone (160 mg/week), but the protocol was discontinued after the first cycle because of intolerance and the appearance of leukocytopenia. Treatment with DARA resulted in a rapid decrease in proteinuria (from 8.2 to 1.9 g/24 h at the 13th dose) with disappearance of Bence–Jones proteinuria and serum M component and normalization of FLC ratio. No infusion related reactions were observed. After the 13thinfusion, the patient was hospitalized for pneumonia and treatment was temporarily discontinued.
4.039063
0.976074
sec[1]/p[6]
en
0.999998
33050272
https://doi.org/10.3390/jcm9103232
[ "proteinuria", "serum", "bortezomib", "bence", "jones", "component", "discontinued", "based", "regimen", "intolerant" ]
[ { "code": "MF96.Z", "title": "Proteinuria, unspecified" }, { "code": "MF96.Y", "title": "Other specified proteinuria" }, { "code": "GB4Y", "title": "Other specified glomerular diseases" }, { "code": "MF96.0", "title": "Orthostatic proteinuria" }, { "code": "JA22.0", "title": "Gestational proteinuria without hypertension" }, { "code": "NE80.3", "title": "Other serum reactions" }, { "code": "5D0Y", "title": "Other specified metabolic disorders" }, { "code": "5B91.0", "title": "Hypercalcaemia" }, { "code": "4A84.Y", "title": "Other specified anaphylaxis" }, { "code": "5C50.F2", "title": "Homocarnosinosis" } ]
=== ICD-11 CODES FOUND === [MF96.Z] Proteinuria, unspecified Also known as: Proteinuria, unspecified | Proteinuria | Albuminuria NOS | Proteinuria NOS [MF96.Y] Other specified proteinuria Also known as: Other specified proteinuria [GB4Y] Other specified glomerular diseases Also known as: Other specified glomerular diseases | Glomerular disease classified by clinical features or syndromes | Chronic proteinuria | Permanent proteinuria with focal and segmental hyalinosis without nephrotic syndrome | Recurrent or persistent glomerular haematuria [MF96.0] Orthostatic proteinuria Definition: A condition characterised by an elevated protein excretion while in the upright position and normal protein excretion in a supine or recumbent position. Also known as: Orthostatic proteinuria | benign postural proteinuria | orthostatic albuminuria | postural albuminuria | postural proteinuria [JA22.0] Gestational proteinuria without hypertension Also known as: Gestational proteinuria without hypertension | proteinuria complicating pregnancy | puerperal albuminuria | Gestational proteinuria, intermittent | Gestational proteinuria, persistent [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 [5B91.0] Hypercalcaemia Definition: Hypercalcaemia is a condition caused by increased calcium levels. The higher the calcium levels and the faster its level rises, the more severe will be the symptoms. When present, symptoms are caused by dehydration secondary to urinary losses of calcium, water and other electrolytes, and to an increase in membrane potential caused by the elevation in extracellular fluid ionized calcium concentration. Patients with moderate to severe hypercalcaemia often complain of nausea and vomiting, symptoms Also known as: Hypercalcaemia | Calcium excess | elevated serum calcium | hypercalcaemic crisis | hypercalcaemic syndrome [4A84.Y] Other specified anaphylaxis Also known as: Other specified anaphylaxis | Latex-induced anaphylaxis | Anaphylaxis due to latex | Latex anaphylaxis | Anaphylactic shock due to serum [5C50.F2] Homocarnosinosis Definition: Homocarnosinosis is a metabolic defect characterised by progressive spastic diplegia, intellectual deficit and retinitis pigmentosa. This extremely rare disorder has been reported in only one family, namely a woman and three of her children. The latter showed but their mother was symptom free. It is therefore uncertain whether there is a relationship between the biochemical defect and the clinical symptoms. Inheritance in the reported family seems to be autosomal dominant. Also known as: Homocarnosinosis | Homocarnosinase deficiency | Serum carnosinase deficiency === GRAPH WALKS === --- Walk 1 --- [MF96.Z] Proteinuria, unspecified --PARENT--> [MF96] Proteinuria Def: Excessive serum proteins in the urine, such as in renal disease when albumin is the main protein, but also may be due to other proteins such as immunoglobulin light chains in plasma cell dyscrasia suc... --EXCLUDES--> [?] Persistent proteinuria or albuminuria Def: Persistent albuminuria >3mg/mmol creatinine or >30mg/day is regarded as abnormal, indicative and often the first manifestation of chronic kidney disease (CKD). In surveillance for CKD in “at risk” pat... --- Walk 2 --- [MF96.Z] Proteinuria, unspecified --PARENT--> [MF96] Proteinuria Def: Excessive serum proteins in the urine, such as in renal disease when albumin is the main protein, but also may be due to other proteins such as immunoglobulin light chains in plasma cell dyscrasia suc... --CHILD--> [MF96.Y] Other specified proteinuria --- Walk 3 --- [MF96.Y] Other specified proteinuria --PARENT--> [MF96] Proteinuria Def: Excessive serum proteins in the urine, such as in renal disease when albumin is the main protein, but also may be due to other proteins such as immunoglobulin light chains in plasma cell dyscrasia suc... --RELATED_TO--> [?] Gestational oedema with proteinuria without hypertension Def: The accumulation of fluid and proteinuria due to the physiological alterations of pregnancy in the absence of hypertension... --- Walk 4 --- [MF96.Y] Other specified proteinuria --PARENT--> [MF96] Proteinuria Def: Excessive serum proteins in the urine, such as in renal disease when albumin is the main protein, but also may be due to other proteins such as immunoglobulin light chains in plasma cell dyscrasia suc... --RELATED_TO--> [?] Gestational oedema with proteinuria without hypertension Def: The accumulation of fluid and proteinuria due to the physiological alterations of pregnancy in the absence of hypertension... --- Walk 5 --- [GB4Y] Other specified glomerular diseases --PARENT--> [?] Glomerular diseases Def: Any disease characterised by pathological changes to the glomerulus.... --CHILD--> [GB41] Nephrotic syndrome Def: A condition characterised by severe proteinuria, greater than 3.5 g/day in an average adult. The substantial loss of protein in the urine results in hypoalbuminaemia and generalised oedema. There is a... --- Walk 6 --- [GB4Y] Other specified glomerular diseases --PARENT--> [?] Glomerular diseases Def: Any disease characterised by pathological changes to the glomerulus.... --RELATED_TO--> [?] Plasmodium malariae malaria with nephropathy Def: Quartan malarial nephropathy is a rare complication of malariae (quartan) malaria, especially occurring in children; it is a glomerulonephritis, usually fatal....
[ "[MF96.Z] Proteinuria, unspecified\n --PARENT--> [MF96] Proteinuria\n Def: Excessive serum proteins in the urine, such as in renal disease when albumin is the main protein, but also may be due to other proteins such as immunoglobulin light chains in plasma cell dyscrasia suc...\n --EXCLUDES--> [?] Persistent proteinuria or albuminuria\n Def: Persistent albuminuria >3mg/mmol creatinine or >30mg/day is regarded as abnormal, indicative and often the first manifestation of chronic kidney disease (CKD). In surveillance for CKD in “at risk” pat...", "[MF96.Z] Proteinuria, unspecified\n --PARENT--> [MF96] Proteinuria\n Def: Excessive serum proteins in the urine, such as in renal disease when albumin is the main protein, but also may be due to other proteins such as immunoglobulin light chains in plasma cell dyscrasia suc...\n --CHILD--> [MF96.Y] Other specified proteinuria", "[MF96.Y] Other specified proteinuria\n --PARENT--> [MF96] Proteinuria\n Def: Excessive serum proteins in the urine, such as in renal disease when albumin is the main protein, but also may be due to other proteins such as immunoglobulin light chains in plasma cell dyscrasia suc...\n --RELATED_TO--> [?] Gestational oedema with proteinuria without hypertension\n Def: The accumulation of fluid and proteinuria due to the physiological alterations of pregnancy in the absence of hypertension...", "[MF96.Y] Other specified proteinuria\n --PARENT--> [MF96] Proteinuria\n Def: Excessive serum proteins in the urine, such as in renal disease when albumin is the main protein, but also may be due to other proteins such as immunoglobulin light chains in plasma cell dyscrasia suc...\n --RELATED_TO--> [?] Gestational oedema with proteinuria without hypertension\n Def: The accumulation of fluid and proteinuria due to the physiological alterations of pregnancy in the absence of hypertension...", "[GB4Y] Other specified glomerular diseases\n --PARENT--> [?] Glomerular diseases\n Def: Any disease characterised by pathological changes to the glomerulus....\n --CHILD--> [GB41] Nephrotic syndrome\n Def: A condition characterised by severe proteinuria, greater than 3.5 g/day in an average adult. The substantial loss of protein in the urine results in hypoalbuminaemia and generalised oedema. There is a...", "[GB4Y] Other specified glomerular diseases\n --PARENT--> [?] Glomerular diseases\n Def: Any disease characterised by pathological changes to the glomerulus....\n --RELATED_TO--> [?] Plasmodium malariae malaria with nephropathy\n Def: Quartan malarial nephropathy is a rare complication of malariae (quartan) malaria, especially occurring in children; it is a glomerulonephritis, usually fatal...." ]
MF96.Z
Proteinuria, unspecified
[ { "from_icd11": "MF96.Z", "icd10_code": "R809", "icd10_title": "Proteinuria, unspecified" }, { "from_icd11": "MF96.Z", "icd10_code": "R803", "icd10_title": "Bence Jones proteinuria" }, { "from_icd11": "MF96.Z", "icd10_code": "R808", "icd10_title": "Other proteinuria" }, { "from_icd11": "MF96.Z", "icd10_code": "R801", "icd10_title": "Persistent proteinuria, unspecified" }, { "from_icd11": "MF96.Z", "icd10_code": "N391", "icd10_title": "" }, { "from_icd11": "MF96.Z", "icd10_code": "R80", "icd10_title": "Proteinuria" }, { "from_icd11": "MF96.0", "icd10_code": "N2889", "icd10_title": "Other specified disorders of kidney and ureter" }, { "from_icd11": "MF96.0", "icd10_code": "N2882", "icd10_title": "Megaloureter" }, { "from_icd11": "MF96.0", "icd10_code": "N2886", "icd10_title": "Ureteritis cystica" }, { "from_icd11": "MF96.0", "icd10_code": "N2881", "icd10_title": "Hypertrophy of kidney" }, { "from_icd11": "MF96.0", "icd10_code": "N2884", "icd10_title": "Pyelitis cystica" }, { "from_icd11": "MF96.0", "icd10_code": "N2885", "icd10_title": "Pyeloureteritis cystica" }, { "from_icd11": "MF96.0", "icd10_code": "N288", "icd10_title": "Other specified disorders of kidney and ureter" }, { "from_icd11": "MF96.0", "icd10_code": "N392", "icd10_title": "" }, { "from_icd11": "JA22.0", "icd10_code": "O1213", "icd10_title": "Gestational proteinuria, third trimester" } ]
R809
Proteinuria, unspecified
All the operations were performed with a fixed plant posterior-stabilized total knee prosthesis in a medial parapatellar approach. A general anesthetic with an adductor canal block was used for all the patients . And appropriate perioperative parenteral antibiotics were administered for infection prophylaxis. High-pressure pulsatile lavage was used to clean the bone surfaces and soft tissues. Before wound closure, all knees received an intraarticular injection of a cocktail containing ropivacaine, morphine, and ketorolac to enhance postoperative analgesia without drain insertion. Elastic compressive dressing was also used. Each patient received the same perioperative regimen: tranexamic acid (TXA), pain control and rehabilitation. All patients received 1-g intravenous tranexamic acid 30 min before skin incision, and a solution of 1-g tranexamic acid in 50-mL normal saline solution was injected into knee articular cavity after closure of the capsule . Multimodal postoperative pain management and accelerated physical therapy were performed as previously described. Low molecular weight heparin was administered subcutaneously 12 h after the operation and was continued for 2 weeks for thrombosis prophylaxis. After recovery from anesthesia, quadriceps femoris muscle isometric contraction was immediately started, and rehabilitation began on the first postoperative day, including muscle power training.
3.994141
0.372559
sec[1]/sec[1]/p[0]
en
0.999998
32843003
https://doi.org/10.1186/s12891-020-03595-6
[ "used", "postoperative", "tranexamic", "acid", "knee", "patients", "perioperative", "prophylaxis", "closure", "pain" ]
[ { "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": "NE81.0Z", "title": "Haemorrhage or haematoma of other or unspecified site complicating a procedure, not elsewhere classified" }, { "code": "NE81.3", "title": "Postsurgical leak" }, { "code": "QF00", "title": "Acquired absence of limb" }, { "code": "DB30.2", "title": "Adhesions of large intestine with obstruction" }, { "code": "MG30.21", "title": "Chronic postsurgical pain" } ]
=== ICD-11 CODES FOUND === [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 [NE81.0Z] Haemorrhage or haematoma of other or unspecified site complicating a procedure, not elsewhere classified Also known as: Haemorrhage or haematoma of other or unspecified site complicating a procedure, not elsewhere classified | Haemorrhage or haematoma complicating a procedure, not elsewhere classified | postoperative haemorrhage | postoperative bleeding | Haemorrhage at any site resulting from a procedure [NE81.3] Postsurgical leak Also known as: Postsurgical leak | postoperative leak | Postsurgical air leak | postoperative air leak | Postsurgical bile leak Excludes: Malfunction or complication of external stoma of digestive organs | Tracheostomy malfunction [QF00] Acquired absence of limb Also known as: Acquired absence of limb | post traumatic loss of limb | postoperative loss of limb | bilateral amputee | amputee Includes: postoperative loss of limb | post traumatic loss of limb Excludes: Other acquired deformities of limbs | Congenital absence of thigh or lower leg with foot present | Congenital absence of both lower leg and foot [DB30.2] Adhesions of large intestine with obstruction Definition: Large bowel obstruction resulting from intraabdominal adhesion due to laparotomy, trauma, and intraabdominal inflammation such as endometriosis. Also known as: Adhesions of large intestine with obstruction | Postoperative obstruction of the large intestine [MG30.21] Chronic postsurgical pain Definition: Chronic postsurgical pain is chronic pain developing or increasing in intensity after a surgical procedure and persisting beyond the healing process, i.e. at least 3 months after surgery. The pain is either localised to the surgical field, projected to the innervation territory of a nerve situated in this area, or referred to a dermatome (after surgery/injury to deep somatic or visceral tissues). Other causes of pain including infection, malignancy etc. need to be excluded as well as pain contin Also known as: Chronic postsurgical pain | postsurgical pain | chronic postoperative pain | chronic postamputation pain | Chronic pain after spinal surgery Includes: Chronic pain after spinal surgery | Chronic pain after herniotomy | Chronic pain after hysterectomy === GRAPH WALKS === --- Walk 1 --- [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--> [QE11.2] 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 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--> [QE11.0] 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 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... --CHILD--> [6C42] Disorders due to use of synthetic cannabinoids Def: Disorders due to use of synthetic cannabinoids are characterised by the pattern and consequences of synthetic cannabinoid use. Synthetic cannabinoids are synthesized diverse chemical compounds that ar... --- 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--> [6C41] Disorders due to use of cannabis Def: Disorders due to use of cannabis are characterised by the pattern and consequences of cannabis use. Cannabis is the collective term for a range of psychoactive preparations of the cannabis plant, Cann... --- 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... --EXCLUDES--> [?] Disorders due to substance use Def: Disorders due to substance use include disorders that result from a single occasion or repeated use of substances that have psychoactive properties, including certain medications. Disorders related to... --- Walk 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... --CHILD--> [?] Harmful pattern of use of cocaine Def: A pattern of use of cocaine that has caused damage to a person’s physical or mental health or has resulted in behaviour leading to harm to the health of others. The pattern of cocaine use is evident o...
[ "[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--> [QE11.2] 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.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...", "[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--> [6C42] Disorders due to use of synthetic cannabinoids\n Def: Disorders due to use of synthetic cannabinoids are characterised by the pattern and consequences of synthetic cannabinoid use. Synthetic cannabinoids are synthesized diverse chemical compounds that ar...", "[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--> [6C41] Disorders due to use of cannabis\n Def: Disorders due to use of cannabis are characterised by the pattern and consequences of cannabis use. Cannabis is the collective term for a range of psychoactive preparations of the cannabis plant, Cann...", "[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 --EXCLUDES--> [?] 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...", "[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 --CHILD--> [?] Harmful pattern of use of cocaine\n Def: A pattern of use of cocaine that has caused damage to a person’s physical or mental health or has resulted in behaviour leading to harm to the health of others. The pattern of cocaine use is evident o..." ]
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
Dense deposit disease (DDD) is an uncommon renal disorder linked to anomalies in the complement bypass pathway, exhibiting an annual incidence of 1–2 cases per million individuals. It predominantly affects children and adolescents and has a dismal prognosis, with approximately 50% of patients advancing to end-stage renal disease (ESRD) within a decade . Clinical manifestations encompass different degrees of hematuria, proteinuria, hypertension, and renal failure. Laboratory tests indicate persistent or recurrent low-complement C3 in the blood , with immunofluorescence revealing C3 deposition in the glomerular basement membrane and mesangial zone, accompanied by minimal or absent immunoglobulin deposition . IgA nephropathy is a glomerulonephritis distinguished by the deposition of IgA immunoglobulins in the glomerular mesangial region. This illness may also present with C3 deposition in the same area and exhibit clinical manifestations akin to DDD, including hematuria, hypertension, or renal failure . The pathological complexity and the challenges in diagnosis and treatment are markedly heightened when both diseases coexist in an individual. We present a rare renal pathological comorbidity: DDD in conjunction with IgA nephropathy, a case that illustrates the characteristic pathological symptoms of both conditions while also elucidating the intricate pathological link that may exist between them.
4.347656
0.833008
sec[0]/p[0]
en
0.999998
39833736
https://doi.org/10.1186/s12887-025-05415-z
[ "renal", "deposition", "pathological", "complement", "manifestations", "hematuria", "hypertension", "failure", "glomerular", "mesangial" ]
[ { "code": "GC2Z&XA6KU8", "title": "Disease of kidney, not elsewhere classified" }, { "code": "GB6Z", "title": "Kidney failure, unspecified" }, { "code": "LB30.1", "title": "Renal dysplasia" }, { "code": "NB92.0Y", "title": "Other specified injury of kidney" }, { "code": "LB30.7", "title": "Ectopic or pelvic kidney" }, { "code": "ME67", "title": "Skin disorder of uncertain or unspecified nature" }, { "code": "9A78.1", "title": "Corneal pigmentations or deposits" }, { "code": "9A61.6", "title": "Conjunctival or subconjunctival degenerations or deposits" }, { "code": "FB40.Y", "title": "Other specified tenosynovitis" }, { "code": "9A77.Y", "title": "Other specified corneal scars or opacities" } ]
=== ICD-11 CODES FOUND === [GB6Z] Kidney failure, unspecified Also known as: Kidney failure, unspecified | nontraumatic kidney injury | renal failure NOS | kidney block | renal impairment NOS [LB30.1] Renal dysplasia Definition: A condition characterised by abnormal development of one or both kidneys. Also known as: Renal dysplasia | congenital renal dysplasia | dysplasia of kidney | dysplastic kidney | Primary renal dysplasia Excludes: Autosomal dominant polycystic kidney disease [NB92.0Y] Other specified injury of kidney Also known as: Other specified injury of kidney | Injury of kidney without open wound into cavity | Injury of kidney with open wound into cavity | Haematoma of kidney | traumatic perirenal haematoma [LB30.7] Ectopic or pelvic kidney Definition: A birth defect characterised by an abnormally positioned kidney; may be asymptomatic or result in urine blockage, infection or kidney stones Also known as: Ectopic or pelvic kidney | Congenital displaced kidney | congenital misplaced kidney | congenital malposition of kidney | congenital prolapsed kidney Includes: Congenital displaced kidney | Malrotation of kidney [ME67] Skin disorder of uncertain or unspecified nature Definition: A category to enable the presence of a skin disorder to be recorded without making assumptions as to the precise nature of the disorder in question. Also known as: Skin disorder of uncertain or unspecified nature | Skin disorder without established diagnosis | change of skin NOS | dermatological disease NOS | dermatological disorder NOS [9A78.1] Corneal pigmentations or deposits Also known as: Corneal pigmentations or deposits | Haematocornea | corneal blood staining | keratohaemia | Kayser-Fleischer ring Includes: Haematocornea | Kayser-Fleischer ring | Krukenberg spindle [9A61.6] Conjunctival or subconjunctival degenerations or deposits Definition: These are the conjunctival/subconjunctival accumulation of some materials and gradual deterioration with impairment or loss of function, caused by injury, disease, or aging. Also known as: Conjunctival or subconjunctival degenerations or deposits | Conjunctival concretions | conjunctival concretion | conjunctival calculus | conjunctival calcification Includes: Conjunctival concretions | Conjunctival cysts or argyrosis | Conjunctival pigmentations [FB40.Y] Other specified tenosynovitis Also known as: Other specified tenosynovitis | Other tenosynovitis or tendinitis | synovitis NOS | Bicipital tendinitis | biceps tendinitis [9A77.Y] Other specified corneal scars or opacities Also known as: Other specified corneal scars or opacities | Corneal infiltrate or haze | Surgically-induced corneal haze | Argentous corneal deposits | Corneal deposits in metabolic disorders === GRAPH WALKS === --- Walk 1 --- [GB6Z] Kidney failure, unspecified --PARENT--> [?] Kidney failure Def: Inability of the kidneys to adequately filter the blood of waste products, with a lower than normal glomerular filtration rate (GFR). Can be abrupt and potentially reversible (acute kidney injury) or ... --EXCLUDES--> [?] Hypertensive renal disease Def: Hypertensive renal disease is a medical condition referring to damage to the kidney due to chronic high blood pressure.... --- Walk 2 --- [GB6Z] Kidney failure, unspecified --PARENT--> [?] Kidney failure Def: Inability of the kidneys to adequately filter the blood of waste products, with a lower than normal glomerular filtration rate (GFR). Can be abrupt and potentially reversible (acute kidney injury) or ... --EXCLUDES--> [?] Hypertensive renal disease Def: Hypertensive renal disease is a medical condition referring to damage to the kidney due to chronic high blood pressure.... --- Walk 3 --- [LB30.1] Renal dysplasia Def: A condition characterised by abnormal development of one or both kidneys.... --PARENT--> [LB30] Structural developmental anomalies of kidneys Def: Any condition caused by failure of the kidneys to correctly develop during the antenatal period.... --CHILD--> [LB30.1] Renal dysplasia Def: A condition characterised by abnormal development of one or both kidneys.... --- Walk 4 --- [LB30.1] Renal dysplasia Def: A condition characterised by abnormal development of one or both kidneys.... --PARENT--> [LB30] Structural developmental anomalies of kidneys Def: Any condition caused by failure of the kidneys to correctly develop during the antenatal period.... --PARENT--> [?] Structural developmental anomalies of the urinary system Def: Any condition caused by failure of the urinary system to correctly develop during the antenatal period.... --- Walk 5 --- [NB92.0Y] Other specified injury of kidney --PARENT--> [NB92.0] Injury of kidney --CHILD--> [NB92.01] Contusion of kidney, major --- Walk 6 --- [NB92.0Y] Other specified injury of kidney --PARENT--> [NB92.0] Injury of kidney --CHILD--> [NB92.02] Laceration of kidney, minor
[ "[GB6Z] Kidney failure, unspecified\n --PARENT--> [?] Kidney failure\n Def: Inability of the kidneys to adequately filter the blood of waste products, with a lower than normal glomerular filtration rate (GFR). Can be abrupt and potentially reversible (acute kidney injury) or ...\n --EXCLUDES--> [?] Hypertensive renal disease\n Def: Hypertensive renal disease is a medical condition referring to damage to the kidney due to chronic high blood pressure....", "[GB6Z] Kidney failure, unspecified\n --PARENT--> [?] Kidney failure\n Def: Inability of the kidneys to adequately filter the blood of waste products, with a lower than normal glomerular filtration rate (GFR). Can be abrupt and potentially reversible (acute kidney injury) or ...\n --EXCLUDES--> [?] Hypertensive renal disease\n Def: Hypertensive renal disease is a medical condition referring to damage to the kidney due to chronic high blood pressure....", "[LB30.1] Renal dysplasia\n Def: A condition characterised by abnormal development of one or both kidneys....\n --PARENT--> [LB30] Structural developmental anomalies of kidneys\n Def: Any condition caused by failure of the kidneys to correctly develop during the antenatal period....\n --CHILD--> [LB30.1] Renal dysplasia\n Def: A condition characterised by abnormal development of one or both kidneys....", "[LB30.1] Renal dysplasia\n Def: A condition characterised by abnormal development of one or both kidneys....\n --PARENT--> [LB30] Structural developmental anomalies of kidneys\n Def: Any condition caused by failure of the kidneys to correctly develop during the antenatal period....\n --PARENT--> [?] Structural developmental anomalies of the urinary system\n Def: Any condition caused by failure of the urinary system to correctly develop during the antenatal period....", "[NB92.0Y] Other specified injury of kidney\n --PARENT--> [NB92.0] Injury of kidney\n --CHILD--> [NB92.01] Contusion of kidney, major", "[NB92.0Y] Other specified injury of kidney\n --PARENT--> [NB92.0] Injury of kidney\n --CHILD--> [NB92.02] Laceration of kidney, minor" ]
GC2Z&XA6KU8
Disease of kidney, not elsewhere classified
[ { "from_icd11": "GB6Z", "icd10_code": "N19", "icd10_title": "Unspecified kidney failure" }, { "from_icd11": "GB6Z", "icd10_code": "N17-N19", "icd10_title": "" }, { "from_icd11": "GB6Z", "icd10_code": "N17", "icd10_title": "Acute kidney failure" }, { "from_icd11": "LB30.1", "icd10_code": "Q614", "icd10_title": "Renal dysplasia" }, { "from_icd11": "LB30.7", "icd10_code": "Q632", "icd10_title": "Ectopic kidney" }, { "from_icd11": "LB30.7", "icd10_code": "Q63", "icd10_title": "Other congenital malformations of kidney" }, { "from_icd11": "ME67", "icd10_code": "L989", "icd10_title": "Disorder of the skin and subcutaneous tissue, unspecified" }, { "from_icd11": "9A78.1", "icd10_code": "H18049", "icd10_title": "Kayser-Fleischer ring, unspecified eye" }, { "from_icd11": "9A78.1", "icd10_code": "H180", "icd10_title": "Corneal pigmentations and deposits" }, { "from_icd11": "9A61.6", "icd10_code": "H111", "icd10_title": "Conjunctival degenerations and deposits" } ]
N19
Unspecified kidney failure
He was transplanted after seven months of waitlist time. Other than the requirement of multiple magnesium and potassium replacements to maintain serum levels, there were no additional anesthetic or operative management issues related to his GS. Subsequent echocardiograms revealed normal graft function. Posttransplant, the use of tacrolimus in the setting of his underlying GS elicited recalcitrant hypomagnesemia. Postoperative course was complicated by ventricular tachycardia without evidence of rejection, reperfusion injury, or coronary artery abnormality. A lidocaine infusion was initiated and subsequently transitioned to enteral amiodarone. Additionally, he developed significant cramping and tetany in his extremities limiting mobility, which improved with higher serum magnesium levels. A magnesium infusion treated both unique postoperative symptoms. Transition to enteral magnesium was challenging with high stool output and resultant metabolic acidosis. Ultimately, he was discharged home 79 days posttransplant (289 hospitalization days including waitlist time) on a regimen of magnesium oxide, magnesium chloride, sodium bicarbonate, and spironolactone, in addition to amiodarone, enalapril, and immunosuppression with steroids, tacrolimus, and mycophenolate mofetil. His neurologic examination continued to improve throughout hospitalization, and at discharge, he had only mild right-sided weakness.
3.851563
0.97998
sec[0]/p[2]
en
0.999997
32645769
https://doi.org/10.1177/2150135120912227
[ "magnesium", "waitlist", "time", "serum", "posttransplant", "tacrolimus", "postoperative", "infusion", "enteral", "amiodarone" ]
[ { "code": "5C64.41", "title": "Hypomagnesaemia" }, { "code": "5C64.4Z", "title": "Disorders of magnesium metabolism, unspecified" }, { "code": "GB90.4Y", "title": "Other specified renal tubular function disorders" }, { "code": "MA18.1", "title": "Abnormal level of blood mineral" }, { "code": "8D40.2", "title": "Myopathy due to nutritional deficiency" }, { "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" } ]
=== ICD-11 CODES FOUND === [5C64.41] Hypomagnesaemia Definition: This is an electrolyte disturbance in which there is an abnormally low level of magnesium in the blood. Normal magnesium levels in humans fall between 1.5 - 2.5 mg/dL. Usually a serum level less than 0.7 mmol/L is used as reference for hypomagnesemia (not hypomagnesia which refers to low magnesium content in food/supplement sources). Also known as: Hypomagnesaemia | Magnesium deficiency | Primary familial hypomagnesaemia | Familial hypokalaemia - hypercalciuria | Familial hypokalaemia - hypomagnesaemia [5C64.4Z] Disorders of magnesium metabolism, unspecified Also known as: Disorders of magnesium metabolism, unspecified | Disorders of magnesium metabolism [GB90.4Y] Other specified renal tubular function disorders Also known as: Other specified renal tubular function disorders | Disorders with impaired tubular function, not elsewhere classified | disorder resulting from renal impairment | disorders resulting from impaired renal function | functional disturbance of kidney [MA18.1] Abnormal level of blood mineral Also known as: Abnormal level of blood mineral | Abnormal blood level of mineral NEC | Abnormal blood level of cobalt | Abnormal blood level of copper | Abnormal blood level of iron Includes: Abnormal blood level of mineral NEC Excludes: nutritional mineral deficiency | Neonatal hypomagnesaemia [8D40.2] Myopathy due to nutritional deficiency Also known as: Myopathy due to nutritional deficiency | Myopathy due to calcium deficiency | Myopathy due to magnesium deficiency [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 === GRAPH WALKS === --- Walk 1 --- [5C64.41] Hypomagnesaemia Def: This is an electrolyte disturbance in which there is an abnormally low level of magnesium in the blood. Normal magnesium levels in humans fall between 1.5 - 2.5 mg/dL. Usually a serum level less than ... --RELATED_TO--> [?] Neonatal hypomagnesaemia Def: Defined as serum magnesium levels less than 0.66 mmol/L (1.6 mg/L) in neonates. Symptoms usually do not develop until serum Magnesium (Mg) levels fall below 0.49 mmol/L (1.2 mg/L). This is usually tra... --PARENT--> [?] Hypomagnesaemia Def: This is an electrolyte disturbance in which there is an abnormally low level of magnesium in the blood. Normal magnesium levels in humans fall between 1.5 - 2.5 mg/dL. Usually a serum level less than ... --- Walk 2 --- [5C64.41] Hypomagnesaemia Def: This is an electrolyte disturbance in which there is an abnormally low level of magnesium in the blood. Normal magnesium levels in humans fall between 1.5 - 2.5 mg/dL. Usually a serum level less than ... --RELATED_TO--> [?] Neonatal hypomagnesaemia Def: Defined as serum magnesium levels less than 0.66 mmol/L (1.6 mg/L) in neonates. Symptoms usually do not develop until serum Magnesium (Mg) levels fall below 0.49 mmol/L (1.2 mg/L). This is usually tra... --PARENT--> [?] Transitory neonatal disorders of calcium or magnesium metabolism Def: A group of paediatric conditions in which there is a temporary disorder in a newborn associated with abnormal chemical reactions in the body disrupting the normal processes of enzyme catalyzed reactio... --- Walk 3 --- [5C64.4Z] Disorders of magnesium metabolism, unspecified --PARENT--> [5C64.4] Disorders of magnesium metabolism Def: Any condition caused by failure to correctly metabolize magnesium.... --CHILD--> [5C64.40] Hypermagnesaemia Def: This is an electrolyte disturbance in which there is an abnormally elevated level of magnesium in the blood. Usually this results in excess of magnesium in the body.... --- Walk 4 --- [5C64.4Z] Disorders of magnesium metabolism, unspecified --PARENT--> [5C64.4] Disorders of magnesium metabolism Def: Any condition caused by failure to correctly metabolize magnesium.... --CHILD--> [5C64.40] Hypermagnesaemia Def: This is an electrolyte disturbance in which there is an abnormally elevated level of magnesium in the blood. Usually this results in excess of magnesium in the body.... --- Walk 5 --- [GB90.4Y] Other specified renal tubular function disorders --PARENT--> [GB90.4] Renal tubular function disorders Def: Disorders primarily due to abnormalities of renal tubular resorption or secretion.... --RELATED_TO--> [?] Cystinuria Def: Cystinuria is a renal tubular aminoacid transport disorder characterised by recurrent formation of kidneys cystine stones.... --- Walk 6 --- [GB90.4Y] Other specified renal tubular function disorders --PARENT--> [GB90.4] Renal tubular function disorders Def: Disorders primarily due to abnormalities of renal tubular resorption or secretion.... --RELATED_TO--> [?] Cystinuria Def: Cystinuria is a renal tubular aminoacid transport disorder characterised by recurrent formation of kidneys cystine stones....
[ "[5C64.41] Hypomagnesaemia\n Def: This is an electrolyte disturbance in which there is an abnormally low level of magnesium in the blood. Normal magnesium levels in humans fall between 1.5 - 2.5 mg/dL. Usually a serum level less than ...\n --RELATED_TO--> [?] Neonatal hypomagnesaemia\n Def: Defined as serum magnesium levels less than 0.66 mmol/L (1.6 mg/L) in neonates. Symptoms usually do not develop until serum Magnesium (Mg) levels fall below 0.49 mmol/L (1.2 mg/L). This is usually tra...\n --PARENT--> [?] Hypomagnesaemia\n Def: This is an electrolyte disturbance in which there is an abnormally low level of magnesium in the blood. Normal magnesium levels in humans fall between 1.5 - 2.5 mg/dL. Usually a serum level less than ...", "[5C64.41] Hypomagnesaemia\n Def: This is an electrolyte disturbance in which there is an abnormally low level of magnesium in the blood. Normal magnesium levels in humans fall between 1.5 - 2.5 mg/dL. Usually a serum level less than ...\n --RELATED_TO--> [?] Neonatal hypomagnesaemia\n Def: Defined as serum magnesium levels less than 0.66 mmol/L (1.6 mg/L) in neonates. Symptoms usually do not develop until serum Magnesium (Mg) levels fall below 0.49 mmol/L (1.2 mg/L). This is usually tra...\n --PARENT--> [?] Transitory neonatal disorders of calcium or magnesium metabolism\n Def: A group of paediatric conditions in which there is a temporary disorder in a newborn associated with abnormal chemical reactions in the body disrupting the normal processes of enzyme catalyzed reactio...", "[5C64.4Z] Disorders of magnesium metabolism, unspecified\n --PARENT--> [5C64.4] Disorders of magnesium metabolism\n Def: Any condition caused by failure to correctly metabolize magnesium....\n --CHILD--> [5C64.40] Hypermagnesaemia\n Def: This is an electrolyte disturbance in which there is an abnormally elevated level of magnesium in the blood. Usually this results in excess of magnesium in the body....", "[5C64.4Z] Disorders of magnesium metabolism, unspecified\n --PARENT--> [5C64.4] Disorders of magnesium metabolism\n Def: Any condition caused by failure to correctly metabolize magnesium....\n --CHILD--> [5C64.40] Hypermagnesaemia\n Def: This is an electrolyte disturbance in which there is an abnormally elevated level of magnesium in the blood. Usually this results in excess of magnesium in the body....", "[GB90.4Y] Other specified renal tubular function disorders\n --PARENT--> [GB90.4] Renal tubular function disorders\n Def: Disorders primarily due to abnormalities of renal tubular resorption or secretion....\n --RELATED_TO--> [?] Cystinuria\n Def: Cystinuria is a renal tubular aminoacid transport disorder characterised by recurrent formation of kidneys cystine stones....", "[GB90.4Y] Other specified renal tubular function disorders\n --PARENT--> [GB90.4] Renal tubular function disorders\n Def: Disorders primarily due to abnormalities of renal tubular resorption or secretion....\n --RELATED_TO--> [?] Cystinuria\n Def: Cystinuria is a renal tubular aminoacid transport disorder characterised by recurrent formation of kidneys cystine stones...." ]
5C64.41
Hypomagnesaemia
[ { "from_icd11": "5C64.41", "icd10_code": "E612", "icd10_title": "Magnesium deficiency" }, { "from_icd11": "5C64.4Z", "icd10_code": "E8342", "icd10_title": "Hypomagnesemia" }, { "from_icd11": "5C64.4Z", "icd10_code": "E8341", "icd10_title": "Hypermagnesemia" }, { "from_icd11": "5C64.4Z", "icd10_code": "E8340", "icd10_title": "Disorders of magnesium metabolism, unspecified" }, { "from_icd11": "5C64.4Z", "icd10_code": "E8349", "icd10_title": "Other disorders of magnesium metabolism" }, { "from_icd11": "5C64.4Z", "icd10_code": "E834", "icd10_title": "Disorders of magnesium metabolism" }, { "from_icd11": "MA18.1", "icd10_code": "R790", "icd10_title": "Abnormal level of blood mineral" }, { "from_icd11": "8D40.2", "icd10_code": "E639", "icd10_title": "Nutritional deficiency, unspecified" }, { "from_icd11": "8D40.2", "icd10_code": "E58", "icd10_title": "Dietary calcium deficiency" }, { "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" } ]
E612
Magnesium deficiency
In January 2015, she presented with a 3-month history of worsening chest pain and rapid bilateral axillary lymph node enlargement. On examination, there was a lymph node of 2 cm diameter on each side of the armpit. On the basis of biopsy result, left axillary lymph node was GS. The immunohistochemistry examination showed bcl-2(+), CD34(+), CD117(+), MPO(+), Lysonzyme(+), TDT(+), Ki67(+5∼10%), CD3(−), CD5(−), CD20(−), P53(−), CD10(−), CD68(−), CD30(−), CD(79), Bcl-6(−), CD21(−), CD56 (−), CD15 (−), ALK (−), CyclinD1 (−), Mum-1 (−), CD23 (−), CD38(−). Peripheral blood smear, bone marrow examinations, and flow cytometry of bone marrow were normal. Conventional cytogenetics of bone marrow revealed a normal karyotype of 46, XX , but PML/RARA fusion gene by reverse transcription-polymerase chain reaction (RT-PCR) was 0.019% . In addition, PML/RARA fusion signal by FISH was positive for lymph node . Computed tomography (CT) scan of chest revealed the increase of bone density in the body of sternum . She received DA regimen (2 cycles) after which no enlarged lymph nodes were found by ultrasonography, and then received another DA, EA (etoposide70 mg/m 2 /day, d1∼4; cytarabine 150 mg/m 2 /day, d1∼7) regimens, and ATRA (25 mg/m 2 /day, d1∼28, 2 cycles). She received prophylactic intrathecal chemotherapy (dexamethasone 10 mg, cytarabine 30 mg, methotrexate 15 mg) during induction and consolidation therapy.
4.03125
0.973145
sec[1]/p[2]
en
0.999996
33832087
https://doi.org/10.1097/MD.0000000000025257
[ "lymph", "node", "bone", "marrow", "chest", "axillary", "rara", "fusion", "cycles", "cytarabine" ]
[ { "code": "BD9Z", "title": "Disorders of lymphatic vessels or lymph nodes, unspecified" }, { "code": "BD90.Z", "title": "Lymphadenitis, unspecified" }, { "code": "BD90.Y", "title": "Other specified lymphadenitis" }, { "code": "BD9Y", "title": "Other specified disorders of lymphatic vessels or lymph nodes" }, { "code": "MA01.Z", "title": "Enlarged lymph nodes, unspecified" }, { "code": "FA20.0", "title": "Seropositive rheumatoid arthritis" }, { "code": "MF30", "title": "Breast lump or mass female" }, { "code": "BB40", "title": "Acute or subacute infectious endocarditis" }, { "code": "FA0Z", "title": "Osteoarthritis, unspecified" }, { "code": "FA85.10", "title": "Localised central endplate defect" } ]
=== ICD-11 CODES FOUND === [BD9Z] Disorders of lymphatic vessels or lymph nodes, unspecified Also known as: Disorders of lymphatic vessels or lymph nodes, unspecified | Lymphatic system disorders | lymph disease NOS | lymph gland disease | Lymphatic system disease NOS [BD90.Z] Lymphadenitis, unspecified Also known as: Lymphadenitis, unspecified | Lymphadenitis | adenitis NOS | inflammation of gland | lymphatic gland inflammation [BD90.Y] Other specified lymphadenitis Also known as: Other specified lymphadenitis | Dermatopathic lymphadenopathy | lipomelanotic reticulosis | Infective inguinal bubo | bubo [BD9Y] Other specified disorders of lymphatic vessels or lymph nodes Also known as: Other specified disorders of lymphatic vessels or lymph nodes | Chylous cyst | Mesentery chylous cyst | Peritoneum chylous cyst | Lymphocele [MA01.Z] Enlarged lymph nodes, unspecified Also known as: Enlarged lymph nodes, unspecified | Enlarged lymph nodes | swollen glands | Lymphadenopathy | adenopathy [FA20.0] Seropositive rheumatoid arthritis Also known as: Seropositive rheumatoid arthritis | high positive rheumatoid factor | low positive rheumatoid factor | high positive anticitrullinated protein antibody | low positive anticitrullinated protein antibody [MF30] Breast lump or mass female Also known as: Breast lump or mass female | breast irregular nodularity | breast node | lump in breast | lump or mass in breast NOS [BB40] Acute or subacute infectious endocarditis Also known as: Acute or subacute infectious endocarditis | subacute infective endocarditis NOS | infective endocarditis NOS | acute infective endocarditis NOS | infectious endocarditis Excludes: Infectious myocarditis [FA0Z] Osteoarthritis, unspecified Also known as: Osteoarthritis, unspecified | osteoarthritis NOS | arthrosis NOS | OA - [osteoarthritis] | Osteoarthritis with determinants [FA85.10] Localised central endplate defect Also known as: Localised central endplate defect | Schmorl nodes | schmorl's nodes | schmorl's nodules === GRAPH WALKS === --- Walk 1 --- [BD9Z] Disorders of lymphatic vessels or lymph nodes, unspecified --PARENT--> [?] Disorders of lymphatic vessels or lymph nodes Def: Disorders due to developmental and acquired disturbances of lymph circulation and drainage and to infective disorders of lymph vessels and nodes.... --CHILD--> [BD91] Lymphangitis Def: Lymphangitis is an inflammation of lymphatic vessels. It is most often caused by infection from bacteria, virus or fungus or infiltration by cancer cells.... --- Walk 2 --- [BD9Z] Disorders of lymphatic vessels or lymph nodes, unspecified --PARENT--> [?] Disorders of lymphatic vessels or lymph nodes Def: Disorders due to developmental and acquired disturbances of lymph circulation and drainage and to infective disorders of lymph vessels and nodes.... --EXCLUDES--> [?] Enlarged lymph nodes Def: Enlarged lymph node is called lymphadenopathy which means the abnormal enlargement of lymph nodes.... --- Walk 3 --- [BD90.Z] Lymphadenitis, unspecified --PARENT--> [BD90] Lymphadenitis --CHILD--> [BD90.0] Acute lymphadenitis --- Walk 4 --- [BD90.Z] Lymphadenitis, unspecified --PARENT--> [BD90] Lymphadenitis --EXCLUDES--> [?] Human immunodeficiency virus disease Def: A case of HIV infection is defined as an individual with HIV infection irrespective of clinical stage including severe or stage 4 clinical disease (also known as AIDS) confirmed by laboratory criteria... --- Walk 5 --- [BD90.Y] Other specified lymphadenitis --PARENT--> [BD90] Lymphadenitis --EXCLUDES--> [?] Human immunodeficiency virus disease Def: A case of HIV infection is defined as an individual with HIV infection irrespective of clinical stage including severe or stage 4 clinical disease (also known as AIDS) confirmed by laboratory criteria... --- Walk 6 --- [BD90.Y] Other specified lymphadenitis --PARENT--> [BD90] Lymphadenitis --CHILD--> [BD90.1] Nonspecific mesenteric lymphadenitis
[ "[BD9Z] Disorders of lymphatic vessels or lymph nodes, unspecified\n --PARENT--> [?] Disorders of lymphatic vessels or lymph nodes\n Def: Disorders due to developmental and acquired disturbances of lymph circulation and drainage and to infective disorders of lymph vessels and nodes....\n --CHILD--> [BD91] Lymphangitis\n Def: Lymphangitis is an inflammation of lymphatic vessels. It is most often caused by infection from bacteria, virus or fungus or infiltration by cancer cells....", "[BD9Z] Disorders of lymphatic vessels or lymph nodes, unspecified\n --PARENT--> [?] Disorders of lymphatic vessels or lymph nodes\n Def: Disorders due to developmental and acquired disturbances of lymph circulation and drainage and to infective disorders of lymph vessels and nodes....\n --EXCLUDES--> [?] Enlarged lymph nodes\n Def: Enlarged lymph node is called lymphadenopathy which means the abnormal enlargement of lymph nodes....", "[BD90.Z] Lymphadenitis, unspecified\n --PARENT--> [BD90] Lymphadenitis\n --CHILD--> [BD90.0] Acute lymphadenitis", "[BD90.Z] Lymphadenitis, unspecified\n --PARENT--> [BD90] Lymphadenitis\n --EXCLUDES--> [?] Human immunodeficiency virus disease\n Def: A case of HIV infection is defined as an individual with HIV infection irrespective of clinical stage including severe or stage 4 clinical disease (also known as AIDS) confirmed by laboratory criteria...", "[BD90.Y] Other specified lymphadenitis\n --PARENT--> [BD90] Lymphadenitis\n --EXCLUDES--> [?] Human immunodeficiency virus disease\n Def: A case of HIV infection is defined as an individual with HIV infection irrespective of clinical stage including severe or stage 4 clinical disease (also known as AIDS) confirmed by laboratory criteria...", "[BD90.Y] Other specified lymphadenitis\n --PARENT--> [BD90] Lymphadenitis\n --CHILD--> [BD90.1] Nonspecific mesenteric lymphadenitis" ]
BD9Z
Disorders of lymphatic vessels or lymph nodes, unspecified
[ { "from_icd11": "BD9Z", "icd10_code": "I898", "icd10_title": "Other specified noninfective disorders of lymphatic vessels and lymph nodes" }, { "from_icd11": "BD9Z", "icd10_code": "I899", "icd10_title": "Noninfective disorder of lymphatic vessels and lymph nodes, unspecified" }, { "from_icd11": "BD9Z", "icd10_code": "I89", "icd10_title": "Other noninfective disorders of lymphatic vessels and lymph nodes" }, { "from_icd11": "BD90.Z", "icd10_code": "I889", "icd10_title": "Nonspecific lymphadenitis, unspecified" }, { "from_icd11": "BD90.Z", "icd10_code": "I88", "icd10_title": "Nonspecific lymphadenitis" }, { "from_icd11": "BD90.Z", "icd10_code": "I888", "icd10_title": "Other nonspecific lymphadenitis" }, { "from_icd11": "BD90.Z", "icd10_code": "L00-L08", "icd10_title": "" }, { "from_icd11": "MA01.Z", "icd10_code": "R599", "icd10_title": "Enlarged lymph nodes, unspecified" }, { "from_icd11": "MA01.Z", "icd10_code": "R59", "icd10_title": "Enlarged lymph nodes" }, { "from_icd11": "FA20.0", "icd10_code": "M0569", "icd10_title": "Rheumatoid arthritis of multiple sites with involvement of other organs and systems" }, { "from_icd11": "FA20.0", "icd10_code": "M0579", "icd10_title": "Rheumatoid arthritis with rheumatoid factor of multiple sites without organ or systems involvement" }, { "from_icd11": "FA20.0", "icd10_code": "M05612", "icd10_title": "Rheumatoid arthritis of left shoulder with involvement of other organs and systems" }, { "from_icd11": "FA20.0", "icd10_code": "M0570", "icd10_title": "Rheumatoid arthritis with rheumatoid factor of unspecified site without organ or systems involvement" }, { "from_icd11": "FA20.0", "icd10_code": "M0560", "icd10_title": "Rheumatoid arthritis of unspecified site with involvement of other organs and systems" }, { "from_icd11": "FA20.0", "icd10_code": "M0500", "icd10_title": "Felty's syndrome, unspecified site" } ]
I898
Other specified noninfective disorders of lymphatic vessels and lymph nodes
Overall, 79% of adult patients with IAE survived with established, evidence-based care . Patients suffered residual neurological defects however which include primarily cognitive deficits and motor weakness in approximately 25% . Those specific symptoms were evident in the immediate three-month period postinsult. Long-term symptoms and sequelae beyond three months are unknown due to under reporting . This patient was transferred to a LTACH facility for a higher level of specialized care. The three-month follow-up shows that this particular patient was nonresponsive. He has occasional episodes of spontaneous eye opening. He was not following verbal command or responding to external stimuli which was also seen in the acute phase of illness. Hypertonicity in all four extremities with significant contractures was noted in the upper extremities and lower extremities. Hypoactive reflexes were also noted on physical examination. CT head in the three-month period after initial insult showed a minimal degree of cerebral and cerebellar cortical atrophy and a minimal degree of central atrophy of the cerebral hemispheres. Decreased attenuation in white matter of both cerebral hemispheres was noted, consistent with demyelination. At that time, no acute findings of hemorrhage or mass effect were seen. At five-month postinsult, the patient did not have any semblance of partial or complete neurologic recovery.
4.054688
0.931152
sec[2]/p[11]
en
0.999997
33425396
https://doi.org/10.1155/2020/6616805
[ "three", "extremities", "cerebral", "patients", "which", "period", "postinsult", "this", "that", "degree" ]
[ { "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" }, { "code": "ND56.1", "title": "Open wound of unspecified body region" }, { "code": "LB9Z", "title": "Structural developmental anomalies of the skeleton, unspecified" }, { "code": "FB56.6", "title": "Other specified soft tissue disorders" }, { "code": "5B51&XS25", "title": "Severe wasting in infants, children or adolescents" }, { "code": "ND55", "title": "Other injuries of leg, level unspecified" } ]
=== ICD-11 CODES FOUND === [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 [ND56.1] Open wound of unspecified body region Also known as: Open wound of unspecified body region | cut NOS | open wound NOS | penetrating wound NOS | Puncture wound with foreign body unspecified body region Excludes: Traumatic amputations involving multiple body regions | Open wounds involving multiple body regions | traumatic amputation NOS [LB9Z] Structural developmental anomalies of the skeleton, unspecified Also known as: Structural developmental anomalies of the skeleton, unspecified | Abnormal bone development | skeletal anomaly NOS [FB56.6] Other specified soft tissue disorders Also known as: Other specified soft tissue disorders | Fat necrosis | fatty necrosis | Profichet's disease | Sloughing of fascia [ND55] Other injuries of leg, level unspecified Also known as: Other injuries of leg, level unspecified | other injuries of lower limb, level unspecified | Superficial injury of leg, level unspecified | Abrasion of leg, level unspecified | Contusion of leg, level unspecified Excludes: Fracture of leg, level unspecified | Injuries involving multiple body regions === GRAPH WALKS === --- Walk 1 --- [1D45] Sandfly fever --PARENT--> [?] Certain arthropod-borne viral fevers --RELATED_TO--> [?] Far Eastern tick-borne encephalitis --- Walk 2 --- [1D45] Sandfly fever --PARENT--> [?] Certain arthropod-borne viral fevers --RELATED_TO--> [?] Far Eastern tick-borne encephalitis --- Walk 3 --- [PA09] Unintentional land transport traffic event injuring an occupant of a low powered passenger vehicle --PARENT--> [?] Unintentional land transport road traffic injury event --CHILD--> [PA01] Unintentional land transport traffic event injuring the user of a pedestrian conveyance --- Walk 4 --- [PA09] Unintentional land transport traffic event injuring an occupant of a low powered passenger vehicle --PARENT--> [?] Unintentional land transport road traffic injury event --CHILD--> [PA01] Unintentional land transport traffic event injuring the user of a pedestrian conveyance --- Walk 5 --- [LD50.Y] Other specified number anomalies of chromosome X --PARENT--> [LD50] Number anomalies of chromosome X --CHILD--> [LD50.0] Turner syndrome Def: Karyotype missing one X chromosome (45,X0 or 45,X0/46,XX mosaicism); gonads: ovaries (streak); phenotype female with short stature, amenorrhea (hypergonadotropic hypogonadism), absence of sexual devel... --- Walk 6 --- [LD50.Y] Other specified number anomalies of chromosome X --PARENT--> [LD50] Number anomalies of chromosome X --CHILD--> [LD50.1] Karyotype 47,XXX Def: Trisomy X is a sex chromosome anomaly with a variable phenotype caused by the presence of an extra X chromosome in females (47,XXX instead of 46,XX). Most individuals are only mildly affected or asymp...
[ "[1D45] Sandfly fever\n --PARENT--> [?] Certain arthropod-borne viral fevers\n --RELATED_TO--> [?] Far Eastern tick-borne encephalitis", "[1D45] Sandfly fever\n --PARENT--> [?] Certain arthropod-borne viral fevers\n --RELATED_TO--> [?] Far Eastern tick-borne encephalitis", "[PA09] Unintentional land transport traffic event injuring an occupant of a low powered passenger vehicle\n --PARENT--> [?] Unintentional land transport road traffic injury event\n --CHILD--> [PA01] Unintentional land transport traffic event injuring the user of a pedestrian conveyance", "[PA09] Unintentional land transport traffic event injuring an occupant of a low powered passenger vehicle\n --PARENT--> [?] Unintentional land transport road traffic injury event\n --CHILD--> [PA01] Unintentional land transport traffic event injuring the user of a pedestrian conveyance", "[LD50.Y] Other specified number anomalies of chromosome X\n --PARENT--> [LD50] Number anomalies of chromosome X\n --CHILD--> [LD50.0] Turner syndrome\n Def: Karyotype missing one X chromosome (45,X0 or 45,X0/46,XX mosaicism); gonads: ovaries (streak); phenotype female with short stature, amenorrhea (hypergonadotropic hypogonadism), absence of sexual devel...", "[LD50.Y] Other specified number anomalies of chromosome X\n --PARENT--> [LD50] Number anomalies of chromosome X\n --CHILD--> [LD50.1] Karyotype 47,XXX\n Def: Trisomy X is a sex chromosome anomaly with a variable phenotype caused by the presence of an extra X chromosome in females (47,XXX instead of 46,XX). Most individuals are only mildly affected or asymp..." ]
1D45
Sandfly fever
[ { "from_icd11": "1D45", "icd10_code": "A931", "icd10_title": "Sandfly fever" }, { "from_icd11": "PA09", "icd10_code": "V30-V39", "icd10_title": "" }, { "from_icd11": "PA09", "icd10_code": "V32", "icd10_title": "Occupant of three-wheeled motor vehicle injured in collision with two- or three-wheeled motor vehicle" }, { "from_icd11": "PA09", "icd10_code": "V329", "icd10_title": "Unspecified occupant of three-wheeled motor vehicle injured in collision with two- or three-wheeled motor vehicle in traffic accident" }, { "from_icd11": "PA09", "icd10_code": "V33", "icd10_title": "Occupant of three-wheeled motor vehicle injured in collision with car, pick-up truck or van" }, { "from_icd11": "PA09", "icd10_code": "V334", "icd10_title": "Person boarding or alighting a three-wheeled motor vehicle injured in collision with car, pick-up truck or van" }, { "from_icd11": "PA09", "icd10_code": "V335", "icd10_title": "Driver of three-wheeled motor vehicle injured in collision with car, pick-up truck or van in traffic accident" }, { "from_icd11": "PA09", "icd10_code": "V336", "icd10_title": "Passenger in three-wheeled motor vehicle injured in collision with car, pick-up truck or van in traffic accident" }, { "from_icd11": "PA09", "icd10_code": "V337", "icd10_title": "Person on outside of three-wheeled motor vehicle injured in collision with car, pick-up truck or van in traffic accident" }, { "from_icd11": "PA09", "icd10_code": "V339", "icd10_title": "Unspecified occupant of three-wheeled motor vehicle injured in collision with car, pick-up truck or van in traffic accident" }, { "from_icd11": "PA09", "icd10_code": "V34", "icd10_title": "Occupant of three-wheeled motor vehicle injured in collision with heavy transport vehicle or bus" }, { "from_icd11": "PA09", "icd10_code": "V349", "icd10_title": "Unspecified occupant of three-wheeled motor vehicle injured in collision with heavy transport vehicle or bus in traffic accident" }, { "from_icd11": "PA09", "icd10_code": "V36", "icd10_title": "Occupant of three-wheeled motor vehicle injured in collision with other nonmotor vehicle" }, { "from_icd11": "PA09", "icd10_code": "V369", "icd10_title": "Unspecified occupant of three-wheeled motor vehicle injured in collision with other nonmotor vehicle in traffic accident" }, { "from_icd11": "PA09", "icd10_code": "V38", "icd10_title": "Occupant of three-wheeled motor vehicle injured in noncollision transport accident" } ]
A931
Sandfly fever
Carotid cavernous fistula (CCF) is an abnormal arteriovenous communication formed between carotid artery and its branches due to the influence of external factors such as trauma, or spontaneous and cavernous sinus, resulting in a series of clinical symptoms and signs associated with the blood stealing and increased venous pressure. The disease is typically caused by head trauma and skull base fracture and has an incidence rate of 1-2.5% in cases of head trauma . Traumatic CCF cases are characteristically unilateral, and those of bilateral traumatic carotid cavernous fistula (TCCF) are extremely rare. The clinical symptoms of CCF are associated with the direction of venous drainage. The most common etiology of ocular venous drainage is characterized by the presence of the “triple syndromes” typically associated with carotid cavernous fistula in a majority of the patients with intracranial vascular murmur, pulsatile exophthalmos, bulbar conjunctival congestion, or edema. Ocular venous drainage will have “triple syndrome” manifested by intracranial vascular murmur, pulsating eyeball, conjunctival hyperemia, or edema, usually associated with carotid cavernous fistula . We believe that this case of bilateral CCF with pertinent symptoms in only one eye is very rare and combined with contralateral oculomotor nerve injury, it may be easily misdiagnosed and missed and, therefore, deserves our attention.
4.269531
0.774902
sec[0]/p[0]
en
0.999995
34736536
https://doi.org/10.1186/s41016-021-00265-x
[ "carotid", "cavernous", "fistula", "associated", "venous", "trauma", "drainage", "typically", "head", "cases" ]
[ { "code": "8D88.Y", "title": "Other specified autonomic neuropathies" }, { "code": "8B10.Y", "title": "Other specified transient ischaemic attack" }, { "code": "2F9A", "title": "Neoplasms of unknown behaviour of endocrine glands" }, { "code": "BD55", "title": "Asymptomatic stenosis of intracranial or extracranial artery" }, { "code": "NA60.00", "title": "Laceration of carotid artery, minor" }, { "code": "9C81.4", "title": "Cavernous sinus syndromes" }, { "code": "GB06.Y", "title": "Other specified disorders of penis" }, { "code": "LA90.10", "title": "Macrocystic lymphatic malformation" }, { "code": "8B22.43", "title": "Carotid cavernous fistula" }, { "code": "NA07.Y", "title": "Other specified intracranial injury" } ]
=== ICD-11 CODES FOUND === [8D88.Y] Other specified autonomic neuropathies Also known as: Other specified autonomic neuropathies | Autonomic neuropathy due to Fabry’s Disease | Autonomic neuropathy due to Refsum’s Disease | Autonomic neuropathy due to Allgrove syndrome | Autonomic neuropathy due to Tangier’s disease [8B10.Y] Other specified transient ischaemic attack Also known as: Other specified transient ischaemic attack | Vertebrobasilar artery syndrome | vertebrobasilar arterial insufficiency | vertebrobasilar insufficiency | vertebro-basilar artery syndrome, course of resolution unspecified [2F9A] Neoplasms of unknown behaviour of endocrine glands Also known as: Neoplasms of unknown behaviour of endocrine glands | endocrine gland tumour NOS | Neoplasms of unknown behaviour of thyroid gland | thyroid gland tumour NOS | Neoplasms of unknown behaviour of adrenal gland [BD55] Asymptomatic stenosis of intracranial or extracranial artery Definition: Stenosis of intracranial or extracranial artery that has not caused TIA or cerebral ischemic stroke. Also known as: Asymptomatic stenosis of intracranial or extracranial artery | stenosis of carotid artery NOS | stenosis of internal carotid artery NOS | stenosis of precerebral arteries, not resulting in cerebral infarction | narrowing of basilar, carotid or vertebral arteries, not resulting in cerebral infarction Includes: narrowing of basilar, carotid or vertebral arteries, not resulting in cerebral infarction Excludes: Transient ischaemic attack | Cerebral ischaemic stroke [NA60.00] Laceration of carotid artery, minor Also known as: Laceration of carotid artery, minor | incomplete transection of carotid artery | laceration of carotid artery NOS | superficial laceration of carotid artery Includes: incomplete transection of carotid artery | laceration of carotid artery NOS | superficial laceration of carotid artery [9C81.4] Cavernous sinus syndromes Also known as: Cavernous sinus syndromes [GB06.Y] Other specified disorders of penis Also known as: Other specified disorders of penis | Other inflammatory disorders of penis | cavernositis | Abscess of corpus cavernosum and penis | abscess of corpus cavernosum [LA90.10] Macrocystic lymphatic malformation Definition: A condition caused by failure of the lymphatic system to correctly develop during the antenatal period. This condition is characterised by large, soft, smooth clear masses under normal or bluish skin. This condition may be associated with cellulitis, bleeding within the malformation, pain, or leakage of lymphatic fluid internally. Also known as: Macrocystic lymphatic malformation | Cavernous lymphangioma | Cavernous lymphatic malformation | Macrocystic lymphangioma | Circumscribed lymphatic malformation [8B22.43] Carotid cavernous fistula Definition: A carotid-cavernous fistula results from an abnormal communication between the arterial and venous systems within the cavernous sinus in the skull. Also known as: Carotid cavernous fistula [NA07.Y] Other specified intracranial injury Also known as: Other specified intracranial injury | Traumatic intracranial haemorrhage, not elsewhere classified | Traumatic cranium cavity haemorrhage | traumatic intracranium haemorrhage | Intracranial haematoma === GRAPH WALKS === --- Walk 1 --- [8D88.Y] Other specified autonomic neuropathies --PARENT--> [8D88] Autonomic neuropathies --CHILD--> [8D88.1] Autonomic neuropathy due to diabetes mellitus Def: Dysfunction of the autonomic nervous system due to diabetes mellitus that presents as functional complications such as resting tachycardia, exercise intolerance, orthostatic hypotension, constipation,... --- Walk 2 --- [8D88.Y] Other specified autonomic neuropathies --PARENT--> [8D88] Autonomic neuropathies --CHILD--> [8D88.0] Autonomic neuropathy due to sodium channelopathies --- Walk 3 --- [8B10.Y] Other specified transient ischaemic attack --PARENT--> [8B10] Transient ischaemic attack Def: Transient episode of focal neurological dysfunction caused by focal brain ischemia without acute infarction in the clinically relevant area of the brain or transient monocular visual loss due to retin... --EXCLUDES--> [?] Transient global amnesia Def: A time-limited episode (lasting up to two days) of short-term memory loss without other signs or symptoms of neurological impairment.... --- Walk 4 --- [8B10.Y] Other specified transient ischaemic attack --PARENT--> [8B10] Transient ischaemic attack Def: Transient episode of focal neurological dysfunction caused by focal brain ischemia without acute infarction in the clinically relevant area of the brain or transient monocular visual loss due to retin... --CHILD--> [8B10.0] Amaurosis fugax Def: A transient episode of acute visual dysfunction caused by retinal ischaemia. Symptoms should resolve completely within 24 hours.... --- Walk 5 --- [2F9A] Neoplasms of unknown behaviour of endocrine glands --PARENT--> [?] Neoplasms of unknown behaviour, except of lymphoid, haematopoietic, central nervous system or related tissues --CHILD--> [2F91] Neoplasms of unknown behaviour of middle ear, respiratory or intrathoracic organs --- Walk 6 --- [2F9A] Neoplasms of unknown behaviour of endocrine glands --PARENT--> [?] Neoplasms of unknown behaviour, except of lymphoid, haematopoietic, central nervous system or related tissues --CHILD--> [2F91] Neoplasms of unknown behaviour of middle ear, respiratory or intrathoracic organs
[ "[8D88.Y] Other specified autonomic neuropathies\n --PARENT--> [8D88] Autonomic neuropathies\n --CHILD--> [8D88.1] Autonomic neuropathy due to diabetes mellitus\n Def: Dysfunction of the autonomic nervous system due to diabetes mellitus that presents as functional complications such as resting tachycardia, exercise intolerance, orthostatic hypotension, constipation,...", "[8D88.Y] Other specified autonomic neuropathies\n --PARENT--> [8D88] Autonomic neuropathies\n --CHILD--> [8D88.0] Autonomic neuropathy due to sodium channelopathies", "[8B10.Y] Other specified transient ischaemic attack\n --PARENT--> [8B10] Transient ischaemic attack\n Def: Transient episode of focal neurological dysfunction caused by focal brain ischemia without acute infarction in the clinically relevant area of the brain or transient monocular visual loss due to retin...\n --EXCLUDES--> [?] Transient global amnesia\n Def: A time-limited episode (lasting up to two days) of short-term memory loss without other signs or symptoms of neurological impairment....", "[8B10.Y] Other specified transient ischaemic attack\n --PARENT--> [8B10] Transient ischaemic attack\n Def: Transient episode of focal neurological dysfunction caused by focal brain ischemia without acute infarction in the clinically relevant area of the brain or transient monocular visual loss due to retin...\n --CHILD--> [8B10.0] Amaurosis fugax\n Def: A transient episode of acute visual dysfunction caused by retinal ischaemia. Symptoms should resolve completely within 24 hours....", "[2F9A] Neoplasms of unknown behaviour of endocrine glands\n --PARENT--> [?] Neoplasms of unknown behaviour, except of lymphoid, haematopoietic, central nervous system or related tissues\n --CHILD--> [2F91] Neoplasms of unknown behaviour of middle ear, respiratory or intrathoracic organs", "[2F9A] Neoplasms of unknown behaviour of endocrine glands\n --PARENT--> [?] Neoplasms of unknown behaviour, except of lymphoid, haematopoietic, central nervous system or related tissues\n --CHILD--> [2F91] Neoplasms of unknown behaviour of middle ear, respiratory or intrathoracic organs" ]
8D88.Y
Other specified autonomic neuropathies
[ { "from_icd11": "2F9A", "icd10_code": "D446", "icd10_title": "Neoplasm of uncertain behavior of carotid body" }, { "from_icd11": "2F9A", "icd10_code": "D447", "icd10_title": "Neoplasm of uncertain behavior of aortic body and other paraganglia" }, { "from_icd11": "2F9A", "icd10_code": "D444", "icd10_title": "Neoplasm of uncertain behavior of craniopharyngeal duct" }, { "from_icd11": "2F9A", "icd10_code": "D449", "icd10_title": "Neoplasm of uncertain behavior of unspecified endocrine gland" }, { "from_icd11": "2F9A", "icd10_code": "D44", "icd10_title": "Neoplasm of uncertain behavior of endocrine glands" }, { "from_icd11": "2F9A", "icd10_code": "D448", "icd10_title": "" }, { "from_icd11": "BD55", "icd10_code": "I6523", "icd10_title": "Occlusion and stenosis of bilateral carotid arteries" }, { "from_icd11": "BD55", "icd10_code": "I6529", "icd10_title": "Occlusion and stenosis of unspecified carotid artery" }, { "from_icd11": "BD55", "icd10_code": "I6522", "icd10_title": "Occlusion and stenosis of left carotid artery" }, { "from_icd11": "BD55", "icd10_code": "I6521", "icd10_title": "Occlusion and stenosis of right carotid artery" }, { "from_icd11": "BD55", "icd10_code": "I6501", "icd10_title": "Occlusion and stenosis of right vertebral artery" }, { "from_icd11": "BD55", "icd10_code": "I6602", "icd10_title": "Occlusion and stenosis of left middle cerebral artery" }, { "from_icd11": "BD55", "icd10_code": "I6502", "icd10_title": "Occlusion and stenosis of left vertebral artery" }, { "from_icd11": "BD55", "icd10_code": "I6601", "icd10_title": "Occlusion and stenosis of right middle cerebral artery" }, { "from_icd11": "BD55", "icd10_code": "I6503", "icd10_title": "Occlusion and stenosis of bilateral vertebral arteries" } ]
D446
Neoplasm of uncertain behavior of carotid body
Systemic corticosteroids have been accepted as the gold standard treatment for ameliorating the clinical symptoms of DRESS. However, they need to be tapered over 6–8 weeks to prevent the relapse of various symptoms . The usage of intravenous immunoglobulin (IVIG) for patients with life-threatening signs such as renal failure or respiratory failure has also been recommended . Meanwhile, some authors have reported the beneficial effects of the concomitant use of N-acetyl cysteine because of its detoxifying capabilities . Alexander et al. reported a dramatic, sustained clinical response to therapeutic plasma exchange after a steroid treatment failed in a pediatric case of DRESS associated with either lamotrigine or bupropion, leading to multiorgan involvement and life-threatening complications of respiratory failure and cardiac arrest . Our patient presented fever and dyspnea initially, and her symptoms progressed to pulmonary insufficiency requiring non-invasive positive pressure ventilator support. Furthermore, our patient developed jaundice with severe liver dysfunction, and the immunosuppressant drugs of mycophenolate and tacolimus were even prescribed after steroid therapy due to hepatic failure. The use of immunosuppressant drugs for DRESS has never previously been reported in the literature. Our patient may thus be the first patient with a case of DRESS treated with immunosuppressant drugs.
4.164063
0.89502
sec[2]/p[5]
en
0.999998
34828776
https://doi.org/10.3390/children8111063
[ "dress", "failure", "immunosuppressant", "drugs", "life", "threatening", "respiratory", "steroid", "systemic", "corticosteroids" ]
[ { "code": "EH65", "title": "DRESS syndrome" }, { "code": "QB85", "title": "Attention to surgical dressings, drains or sutures" }, { "code": "QF24", "title": "Difficulty or need for assistance with self-care" }, { "code": "DA96.05", "title": "Intestinal failure" }, { "code": "MG4A", "title": "Multi organ failure" }, { "code": "CB41", "title": "Respiratory failure" }, { "code": "CB41.2Z", "title": "Respiratory failure, unspecified" }, { "code": "GB6Z", "title": "Kidney failure, unspecified" }, { "code": "NE60", "title": "Harmful effects of drugs, medicaments or biological substances, not elsewhere classified" }, { "code": "1E83", "title": "Wart virus proliferation in immune-deficient states" } ]
=== ICD-11 CODES FOUND === [EH65] DRESS syndrome Definition: DRESS syndrome (Drug Rash with Eosinophilia and Systemic Symptoms) is a hypersensitivity reaction characterised by a generalised skin rash, fever, eosinophilia, lymphocytosis and visceral involvement (hepatitis, nephritis, pneumonitis, pericarditis and myocarditis) and, in some patients, reactivation of human herpes virus 6. Also known as: DRESS syndrome | Drug-induced hypersensitivity syndrome | DIHS - [drug-induced hypersensitivity syndrome] | Drug rash with eosinophilia and systemic symptoms Includes: Drug-induced hypersensitivity syndrome [QB85] Attention to surgical dressings, drains or sutures Also known as: Attention to surgical dressings, drains or sutures | Change of dressing | Change of suture | Removal of drain | Removal of dressing [QF24] Difficulty or need for assistance with self-care Also known as: Difficulty or need for assistance with self-care | difficulty with self-care | need for assistance with personal care | need for assistance with self-care | Difficulty or need for assistance with dressing [DA96.05] Intestinal failure Definition: The reduction of gut function below the minimum necessary for the absorption of macronutrients and/or water and electrolytes, such that intravenous supplementation is required to maintain health and/or growth. Also known as: Intestinal failure [MG4A] Multi organ failure Definition: Failure of function of more than one organ or organ system, not otherwise specified Also known as: Multi organ failure | MODS - [multi organ dysfunction syndrome] | multiple organ failure | multisystem organ failure | multiorgan failure syndrome [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 [GB6Z] Kidney failure, unspecified Also known as: Kidney failure, unspecified | nontraumatic kidney injury | renal failure NOS | kidney block | renal impairment 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 [1E83] Wart virus proliferation in immune-deficient states Definition: Enhanced proliferation of human papillomavirus as a result of a failure of immune surveillance. This may be due to a genetic defect, disease or iatrogenic immunosuppression. Also known as: Wart virus proliferation in immune-deficient states | Epidermodysplasia verruciformis | Viral warts due to iatrogenic immunosuppression | Viral warts in transplant recipients | Viral warts due to acquired immunodeficiency === GRAPH WALKS === --- Walk 1 --- [EH65] DRESS syndrome Def: DRESS syndrome (Drug Rash with Eosinophilia and Systemic Symptoms) is a hypersensitivity reaction characterised by a generalised skin rash, fever, eosinophilia, lymphocytosis and visceral involvement ... --PARENT--> [?] Drug eruptions --RELATED_TO--> [?] Drug-associated immune complex vasculitis Def: Small vessel vasculitis typically presenting predominantly in the skin due to systemic exposure to certain drugs in predisposed individuals.... --- Walk 2 --- [EH65] DRESS syndrome Def: DRESS syndrome (Drug Rash with Eosinophilia and Systemic Symptoms) is a hypersensitivity reaction characterised by a generalised skin rash, fever, eosinophilia, lymphocytosis and visceral involvement ... --PARENT--> [?] Drug eruptions --CHILD--> [EH62] Lichenoid drug eruption --- Walk 3 --- [QB85] Attention to surgical dressings, drains or sutures --PARENT--> [?] Contact with health services for specific surgical interventions --EXCLUDES--> [?] Contact with health services for purposes of examination or investigation --- Walk 4 --- [QB85] Attention to surgical dressings, drains or sutures --PARENT--> [?] Contact with health services for specific surgical interventions --CHILD--> [QB81] Contact with health services for plastic surgery for unacceptable cosmetic appearance other than hair transplant --- Walk 5 --- [QF24] Difficulty or need for assistance with self-care --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 6 --- [QF24] Difficulty or need for assistance with self-care --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
[ "[EH65] DRESS syndrome\n Def: DRESS syndrome (Drug Rash with Eosinophilia and Systemic Symptoms) is a hypersensitivity reaction characterised by a generalised skin rash, fever, eosinophilia, lymphocytosis and visceral involvement ...\n --PARENT--> [?] Drug eruptions\n --RELATED_TO--> [?] Drug-associated immune complex vasculitis\n Def: Small vessel vasculitis typically presenting predominantly in the skin due to systemic exposure to certain drugs in predisposed individuals....", "[EH65] DRESS syndrome\n Def: DRESS syndrome (Drug Rash with Eosinophilia and Systemic Symptoms) is a hypersensitivity reaction characterised by a generalised skin rash, fever, eosinophilia, lymphocytosis and visceral involvement ...\n --PARENT--> [?] Drug eruptions\n --CHILD--> [EH62] Lichenoid drug eruption", "[QB85] Attention to surgical dressings, drains or sutures\n --PARENT--> [?] Contact with health services for specific surgical interventions\n --EXCLUDES--> [?] Contact with health services for purposes of examination or investigation", "[QB85] Attention to surgical dressings, drains or sutures\n --PARENT--> [?] Contact with health services for specific surgical interventions\n --CHILD--> [QB81] Contact with health services for plastic surgery for unacceptable cosmetic appearance other than hair transplant", "[QF24] Difficulty or need for assistance with self-care\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", "[QF24] Difficulty or need for assistance with self-care\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" ]
EH65
DRESS syndrome
[ { "from_icd11": "EH65", "icd10_code": "L270", "icd10_title": "Generalized skin eruption due to drugs and medicaments taken internally" }, { "from_icd11": "QB85", "icd10_code": "Z481", "icd10_title": "Encounter for planned postprocedural wound closure" }, { "from_icd11": "QB85", "icd10_code": "Z4821", "icd10_title": "Encounter for aftercare following heart transplant" }, { "from_icd11": "QB85", "icd10_code": "Z483", "icd10_title": "Aftercare following surgery for neoplasm" }, { "from_icd11": "QB85", "icd10_code": "Z4823", "icd10_title": "Encounter for aftercare following liver transplant" }, { "from_icd11": "QB85", "icd10_code": "Z4822", "icd10_title": "Encounter for aftercare following kidney transplant" }, { "from_icd11": "QB85", "icd10_code": "Z48298", "icd10_title": "Encounter for aftercare following other organ transplant" }, { "from_icd11": "QB85", "icd10_code": "Z4802", "icd10_title": "Encounter for removal of sutures" }, { "from_icd11": "QB85", "icd10_code": "Z4803", "icd10_title": "Encounter for change or removal of drains" }, { "from_icd11": "QB85", "icd10_code": "Z4801", "icd10_title": "Encounter for change or removal of surgical wound dressing" }, { "from_icd11": "QB85", "icd10_code": "Z4800", "icd10_title": "Encounter for change or removal of nonsurgical wound dressing" }, { "from_icd11": "QB85", "icd10_code": "Z48", "icd10_title": "Encounter for other postprocedural aftercare" }, { "from_icd11": "QB85", "icd10_code": "Z480", "icd10_title": "Encounter for attention to dressings, sutures and drains" }, { "from_icd11": "QF24", "icd10_code": "Z742", "icd10_title": "Need for assistance at home and no other household member able to render care" }, { "from_icd11": "QF24", "icd10_code": "Z741", "icd10_title": "Need for assistance with personal care" } ]
L270
Generalized skin eruption due to drugs and medicaments taken internally
Idiopathic dilatation of the pulmonary artery (IDPA) is a rare condition characterized by enlargement of the pulmonary artery in the absence of an obvious trigger with an incidence of 1 per 14,000 autopsies . The diagnostic criteria for IDPA are (1) diastolic change of the pulmonary artery mainstem; (2) no abnormal shunt inside or outside the heart; (3) no lesions of the arteries that could cause histological changes, such as syphilis and arteriosclerosis; (4) no chronic heart or lung disease; and (5) normal right ventricular pressure. Generally, a patient who meets all the above-mentioned criteria is diagnosed with IDPA. Dilatation of the pulmonary artery may be secondary to an underlying disorder, such as congenital heart disease (including patent ductus arteriosus), chronic heart failure, chronic respiratory disease, vasculitis, Marfan syndrome, and trauma. Given the potential complications associated with IDPA, such as rupture of the pulmonary artery , pulmonary valve insufficiency , and myocardial ischemia due to displacement of the coronary arteries , surgery is a valid option for the treatment of this condition. Although there are several reports on surgery for dilated pulmonary arteries, few have explored the feasibility of anesthetic management for IDPA . We present a case of IDPA complicated by an extracardiac abnormality (Kommerell’s diverticulum), and discuss the management of IDPA.
4.230469
0.891113
sec[0]/p[0]
en
0.999996
33398467
https://doi.org/10.1186/s40981-020-00404-w
[ "pulmonary", "idpa", "artery", "heart", "arteries", "dilatation", "criteria", "idiopathic", "rare", "characterized" ]
[ { "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": "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" } ]
=== 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 [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 === GRAPH WALKS === --- Walk 1 --- [CB40.Y] Other specified diseases of the respiratory system --PARENT--> [CB40] Certain diseases of the respiratory system --RELATED_TO--> [?] Airway obstruction in the neonate due to airway abnormality --- Walk 2 --- [CB40.Y] Other specified diseases of the respiratory system --PARENT--> [CB40] Certain diseases of the respiratory system --RELATED_TO--> [?] 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.... --PARENT--> [?] Structural developmental anomalies of the respiratory system --- 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 ... --CHILD--> [CA40.2] Fungal pneumonia --- 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 ... --RELATED_TO--> [?] Congenital pneumonia Def: Congenital pneumonia is an acute respiratory infection contracted prenatally or during the intrapartum period that is caused by a virus, bacteria, or fungi....
[ "[CB40.Y] Other specified diseases of the respiratory system\n --PARENT--> [CB40] Certain diseases of the respiratory system\n --RELATED_TO--> [?] Airway obstruction in the neonate due to airway abnormality", "[CB40.Y] Other specified diseases of the respiratory system\n --PARENT--> [CB40] Certain diseases of the respiratory system\n --RELATED_TO--> [?] 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 --PARENT--> [?] Structural developmental anomalies of the respiratory system", "[CA40.Z] Pneumonia, organism unspecified\n --PARENT--> [CA40] Pneumonia\n Def: A disease of the lungs, frequently but not always caused by an infection with bacteria, virus, fungus, or parasite. This disease is characterised by fever, chills, cough with sputum production, chest ...\n --CHILD--> [CA40.2] Fungal pneumonia", "[CA40.Z] Pneumonia, organism unspecified\n --PARENT--> [CA40] Pneumonia\n Def: A disease of the lungs, frequently but not always caused by an infection with bacteria, virus, fungus, or parasite. This disease is characterised by fever, chills, cough with sputum production, chest ...\n --RELATED_TO--> [?] Congenital pneumonia\n Def: Congenital pneumonia is an acute respiratory infection contracted prenatally or during the intrapartum period that is caused by a virus, bacteria, or fungi...." ]
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
A 76-year-old male with a history of BCC and squamous cell carcinoma presented to clinic for Mohs micrographic surgery to extirpate a biopsy-proven BCC, two weeks after initial biopsy . Mohs surgery was performed with frozen sections, and the first stage revealed atypical basaloid cells surrounding atypical foamy cells with scalloped nuclei at the deep margin, concerning for SC . The atypical cells were cleared on the second stage, leaving a 2.2 x 1.4 cm surgical defect size. Though SC was favored, given the equivocal pathology on frozen section (BCC with adnexal differentiation vs SC), these slides were sent to dermatopathology for tumor confirmation. A dermatopathologist re-examined the initial biopsy slide, and confirmed nodular BCC alone to be present, as seen in Figure 1A , with morphologic features being distinct and different from the sebaceous carcinoma . The first Mohs stage was re-embedded for permanent sectioning and immunohistochemical staining. SC at the deep margin was confirmed as seen in Figures 1B - 1D , as well the presence of a separate focus of BCC extending into the superficial dermis, as seen in Figure 1B and Figure 1E . The dermatopathologist agreed with the diagnosis of sebaceous carcinoma and favored this to be a collision lesion rather than a contiguous BCC with sebaceous differentiation. The patient continues to follow up at six-month intervals for tumor surveillance.
4.007813
0.977539
sec[1]/p[0]
en
0.999996
34667690
https://doi.org/10.7759/cureus.18015
[ "carcinoma", "mohs", "biopsy", "stage", "atypical", "cells", "sebaceous", "frozen", "margin", "favored" ]
[ { "code": "2D41", "title": "Unspecified carcinoma of unspecified site" }, { "code": "2C3Y", "title": "Other specified malignant neoplasms of skin" }, { "code": "2E6Z", "title": "Carcinoma in situ of unspecified site" }, { "code": "2C25.5", "title": "Unspecified malignant epithelial neoplasm of bronchus or lung" }, { "code": "2C90.Y", "title": "Other specified malignant neoplasms of kidney, except renal pelvis" }, { "code": "8A84.Y", "title": "Other specified secondary headache" }, { "code": "JA85.Y", "title": "Maternal care for other specified fetal abnormality or damage" }, { "code": "KD39.3", "title": "Fetus or newborn affected by complications of fetal surgery" }, { "code": "PK81.5", "title": "Biopsy procedure, not elsewhere classified, associated with injury or harm in therapeutic use" }, { "code": "PK81.4", "title": "Bone marrow aspiration or biopsy associated with injury or harm in therapeutic use" } ]
=== ICD-11 CODES FOUND === [2D41] Unspecified carcinoma of unspecified site Also known as: Unspecified carcinoma of unspecified site | carcinoma of unspecified primary site | carcinoma NOS | Carcinoma in polyp of unspecified site | Carcinoma with apocrine metaplasia of unspecified site [2C3Y] Other specified malignant neoplasms of skin Also known as: Other specified malignant neoplasms of skin | Malignant neoplasm of eyelid NOS | Malignant pilonidal cyst | Radiotherapy-induced skin malignancy | Cutaneous carcinoma [2E6Z] Carcinoma in situ of unspecified site Also known as: Carcinoma in situ of unspecified site | carcinoma in situ of unspecified site | carcinoma in situ NOS | carcinoma in situ | in situ neoplasm [2C25.5] Unspecified malignant epithelial neoplasm of bronchus or lung Also known as: Unspecified malignant epithelial neoplasm of bronchus or lung | unspecified carcinoma of bronchus or lung | Metastatic lung carcinoma [primary lung carcinoma spreading elsewhere] | Metastatic carcinoma of lung [primary carcinoma of lung spreading elsewhere] | Lung carcinoma [2C90.Y] Other specified malignant neoplasms of kidney, except renal pelvis Also known as: Other specified malignant neoplasms of kidney, except renal pelvis | Congenital mesoblastic nephroma | Nephroblastoma | Wilms tumour of kidney | Wilms tumour of unspecified site Includes: Nephroblastoma [8A84.Y] Other specified secondary headache Also known as: Other specified secondary headache | Headache associated with injury to the head or neck | Post traumatic headache | Headache associated with craniotomy | Acute headache associated with craniotomy [JA85.Y] Maternal care for other specified fetal abnormality or damage Also known as: Maternal care for other specified fetal abnormality or damage | Maternal care for damage to fetus from alcohol | suspected damage to fetus from maternal alcohol addiction affecting management of mother | pregnancy management affected by fetal damage from maternal alcohol addiction | maternal care for known or suspected damage to fetus from alcohol [KD39.3] Fetus or newborn affected by complications of fetal surgery Definition: A condition in the fetus due to an unfavourable evolution of a condition (complication) associated with a surgical health intervention applied to the fetus. Also known as: Fetus or newborn affected by complications of fetal surgery | Adverse outcome following fetal skin biopsy [PK81.5] Biopsy procedure, not elsewhere classified, associated with injury or harm in therapeutic use Also known as: Biopsy procedure, not elsewhere classified, associated with injury or harm in therapeutic use | complication during or following biopsy procedure, other than bone marrow Excludes: Bone marrow aspiration or biopsy associated with injury or harm in therapeutic use | Circumstances associated with a surgical or other medical procedure influencing the episode of care, without injury or harm [PK81.4] Bone marrow aspiration or biopsy associated with injury or harm in therapeutic use Also known as: Bone marrow aspiration or biopsy associated with injury or harm in therapeutic use | complication during or following bone marrow aspiration or biopsy Excludes: Circumstances associated with a surgical or other medical procedure influencing the episode of care, without injury or harm === GRAPH WALKS === --- Walk 1 --- [2D41] Unspecified carcinoma of unspecified site --PARENT--> [?] Malignant neoplasms of ill-defined or unspecified primary sites --PARENT--> [?] Malignant neoplasms, except primary neoplasms of lymphoid, haematopoietic, central nervous system or related tissues --- Walk 2 --- [2D41] Unspecified carcinoma of unspecified site --PARENT--> [?] Malignant neoplasms of ill-defined or unspecified primary sites --CHILD--> [2D42] Malignant neoplasms of ill-defined sites Def: Malignant neoplasms of ill defined sites is used for cases where the documentation refers to a site that includes multiple organ systems and tissue types that should be coded separately.... --- Walk 3 --- [2C3Y] Other specified malignant neoplasms of skin --PARENT--> [?] Malignant neoplasms of skin Def: A primary or metastatic tumour involving the skin. Primary malignant skin tumours most often are carcinomas (either basal cell or squamous cell carcinomas that arise from cells in the epidermis) or me... --CHILD--> [2C32] Basal cell carcinoma of skin Def: Basal cell carcinoma or BCC is the most common malignancy in humans. It is believed that BCCs arise from pluripotential cells in the basal layer of the epidermis or, less commonly, hair follicle. BCCs... --- Walk 4 --- [2C3Y] Other specified malignant neoplasms of skin --PARENT--> [?] Malignant neoplasms of skin Def: A primary or metastatic tumour involving the skin. Primary malignant skin tumours most often are carcinomas (either basal cell or squamous cell carcinomas that arise from cells in the epidermis) or me... --EXCLUDES--> [?] Malignant mesenchymal neoplasms Def: A usually aggressive malignant mesenchymal cell tumour most commonly arising from muscle, fat, fibrous tissue, bone, cartilage, and blood vessels. Sarcomas occur in both children and adults. The progn... --- Walk 5 --- [2E6Z] Carcinoma in situ of unspecified site --PARENT--> [?] In situ neoplasms, except of lymphoid, haematopoietic, central nervous system or related tissues --CHILD--> [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 --CHILD--> [2E60] Carcinoma in situ of oral cavity, oesophagus or stomach
[ "[2D41] Unspecified carcinoma of unspecified site\n --PARENT--> [?] Malignant neoplasms of ill-defined or unspecified primary sites\n --PARENT--> [?] Malignant neoplasms, except primary neoplasms of lymphoid, haematopoietic, central nervous system or related tissues", "[2D41] Unspecified carcinoma of unspecified site\n --PARENT--> [?] Malignant neoplasms of ill-defined or unspecified primary sites\n --CHILD--> [2D42] Malignant neoplasms of ill-defined sites\n Def: Malignant neoplasms of ill defined sites is used for cases where the documentation refers to a site that includes multiple organ systems and tissue types that should be coded separately....", "[2C3Y] Other specified malignant neoplasms of skin\n --PARENT--> [?] Malignant neoplasms of skin\n Def: A primary or metastatic tumour involving the skin. Primary malignant skin tumours most often are carcinomas (either basal cell or squamous cell carcinomas that arise from cells in the epidermis) or me...\n --CHILD--> [2C32] Basal cell carcinoma of skin\n Def: Basal cell carcinoma or BCC is the most common malignancy in humans. It is believed that BCCs arise from pluripotential cells in the basal layer of the epidermis or, less commonly, hair follicle. BCCs...", "[2C3Y] Other specified malignant neoplasms of skin\n --PARENT--> [?] Malignant neoplasms of skin\n Def: A primary or metastatic tumour involving the skin. Primary malignant skin tumours most often are carcinomas (either basal cell or squamous cell carcinomas that arise from cells in the epidermis) or me...\n --EXCLUDES--> [?] Malignant mesenchymal neoplasms\n Def: A usually aggressive malignant mesenchymal cell tumour most commonly arising from muscle, fat, fibrous tissue, bone, cartilage, and blood vessels. Sarcomas occur in both children and adults. The progn...", "[2E6Z] Carcinoma in situ of unspecified site\n --PARENT--> [?] In situ neoplasms, except of lymphoid, haematopoietic, central nervous system or related tissues\n --CHILD--> [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 --CHILD--> [2E60] Carcinoma in situ of oral cavity, oesophagus or stomach" ]
2D41
Unspecified carcinoma of unspecified site
[ { "from_icd11": "2E6Z", "icd10_code": "D098", "icd10_title": "Carcinoma in situ of other specified sites" }, { "from_icd11": "2E6Z", "icd10_code": "D099", "icd10_title": "Carcinoma in situ, unspecified" }, { "from_icd11": "2E6Z", "icd10_code": "D00-D09", "icd10_title": "" }, { "from_icd11": "2E6Z", "icd10_code": "D09", "icd10_title": "Carcinoma in situ of other and unspecified sites" }, { "from_icd11": "2E6Z", "icd10_code": "D097", "icd10_title": "" }, { "from_icd11": "JA85.Y", "icd10_code": "O358XX0 ", "icd10_title": "" }, { "from_icd11": "JA85.Y", "icd10_code": "O358XX1 ", "icd10_title": "" } ]
D098
Carcinoma in situ of other specified sites
At that point, he was wheelchair dependent, having spastic quadriparesis with continued spells of seizures despite the therapy with high doses of levetiracetam and clobazam. The patient was continued on clonidine, baclofen, and gabapentin. We started him on a trial of high dose biotin (5 mg/kg/day divided three times a day) and thiamine (100 mg three times a day) for suspected biotin-thiamine-responsive basal ganglia disease (BTBGD) despite the absence of pathogenic variants in the whole-exome sequence (WES) result given the devastating neurologic impairment and low side effect profile of biotin and thiamine. The caregiver reported a significant improvement in awareness, non-verbal communication, spontaneous movement, and spasticity. A mitochondrial genome panel tested was unremarkable. A follow-up brain MRI, almost a year after, did not show new brain lesions; however, interval development of cystic encephalomalacia was noted in the bilateral posterior frontal lobe, insular cortex, and bilateral thalami, and ventricles were noted to be more enlarged in size . Moreover, volume loss was noted in the left hippocampus and body the of corpus callosum . A repeated anti-NMDA IgG antibodies test in serum was positive a year after the initial presentation. Currently, the patient is three years old with stable neurologic impairment, seizure control, and unreported relapse since the initial presentation.
3.955078
0.981934
sec[1]/p[2]
en
0.999996
34692314
https://doi.org/10.7759/cureus.18103
[ "biotin", "three", "thiamine", "despite", "times", "neurologic", "impairment", "brain", "that", "point" ]
[ { "code": "5B5G", "title": "Biotin deficiency" }, { "code": "4B4Y", "title": "Other specified diseases of the immune system" }, { "code": "5C63.Y", "title": "Other specified disorders of vitamin or non-protein cofactor absorption or transport" }, { "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" }, { "code": "5B5A.Z", "title": "Vitamin B1 deficiency, unspecified" }, { "code": "5B5A.00", "title": "Dry beriberi" } ]
=== ICD-11 CODES FOUND === [5B5G] Biotin deficiency Definition: Isolated biotin deficiency is rare. Signs of biotin deficiency in humans have been demonstrated in individuals who consume raw egg white over long periods and in total parenteral nutrition (TPN) before biotin supplementation in patients with malabsorption. The clinical findings of biotin deficiency include dermatitis, conjunctivitis, alopecia, and central nervous system abnormalities. In adults fed raw egg white (which contains avidin, a protein that binds biotin with such high affinity that it Also known as: Biotin deficiency | biotan vitamin deficiency | biotin deficiency disease [4B4Y] Other specified diseases of the immune system Also known as: Other specified diseases of the immune system | Immunodeficiencies | Biotin-dependent carboxylase deficiency [5C63.Y] Other specified disorders of vitamin or non-protein cofactor absorption or transport Also known as: Other specified disorders of vitamin or non-protein cofactor absorption or transport | Disorders of metabolism or transport of other vitamins or cofactors | Biotin-responsive basal ganglia disease | Hereditary hypercarotenaemia or vitamin A deficiency | Pyridoxal phosphate-responsive seizures [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 [5B5A.Z] Vitamin B1 deficiency, unspecified Also known as: Vitamin B1 deficiency, unspecified | Vitamin B1 deficiency | aneurin deficiency | thiamine vitamin deficiency | thiamine deficiency [5B5A.00] Dry beriberi Definition: Neuritic form of beriberi. Also known as: Dry beriberi | Beriberi neuropathy | multiplex endemica neuritis | neuropathic beriberi | neuropathy due to vitamin B1 deficiency === GRAPH WALKS === --- Walk 1 --- [5B5G] Biotin deficiency Def: Isolated biotin deficiency is rare. Signs of biotin deficiency in humans have been demonstrated in individuals who consume raw egg white over long periods and in total parenteral nutrition (TPN) befor... --PARENT--> [?] Undernutrition Def: Undernutrition is a condition in which the body’s requirements are unmet due to underconsumption or to impaired absorption and use of nutrients. It can be produced by lack of access to food, or as a c... --RELATED_TO--> [?] Malnutrition in pregnancy Def: A condition caused by ingestion of a diet in which the nutrients are lacking or are in excess.... --- Walk 2 --- [5B5G] Biotin deficiency Def: Isolated biotin deficiency is rare. Signs of biotin deficiency in humans have been demonstrated in individuals who consume raw egg white over long periods and in total parenteral nutrition (TPN) befor... --PARENT--> [?] Undernutrition Def: Undernutrition is a condition in which the body’s requirements are unmet due to underconsumption or to impaired absorption and use of nutrients. It can be produced by lack of access to food, or as a c... --RELATED_TO--> [?] Fetal intrauterine malnutrition without mention of small for gestational age Def: Neonate, not light or small for gestational age, showing signs of fetal malnutrition, such as dry, peeling skin or loss of subcutaneous tissue.... --- Walk 3 --- [4B4Y] Other specified diseases of the immune system --PARENT--> [04] Diseases of the immune system --CHILD--> [4A20] Acquired immunodeficiencies --- Walk 4 --- [4B4Y] Other specified diseases of the immune system --PARENT--> [04] Diseases of the immune system --EXCLUDES--> [?] Neoplasms Def: An abnormal or uncontrolled cellular proliferation which is not coordinated with an organism's requirements for normal tissue growth, replacement or repair.... --- Walk 5 --- [5C63.Y] Other specified disorders of vitamin or non-protein cofactor absorption or transport --PARENT--> [5C63] Disorders of vitamin or non-protein cofactor absorption or transport --CHILD--> [5C63.1] Disorders of folate metabolism or transport --- Walk 6 --- [5C63.Y] Other specified disorders of vitamin or non-protein cofactor absorption or transport --PARENT--> [5C63] Disorders of vitamin or non-protein cofactor absorption or transport --CHILD--> [5C63.2] Disorders of vitamin D metabolism or transport
[ "[5B5G] Biotin deficiency\n Def: Isolated biotin deficiency is rare. Signs of biotin deficiency in humans have been demonstrated in individuals who consume raw egg white over long periods and in total parenteral nutrition (TPN) befor...\n --PARENT--> [?] Undernutrition\n Def: Undernutrition is a condition in which the body’s requirements are unmet due to underconsumption or to impaired absorption and use of nutrients. It can be produced by lack of access to food, or as a c...\n --RELATED_TO--> [?] Malnutrition in pregnancy\n Def: A condition caused by ingestion of a diet in which the nutrients are lacking or are in excess....", "[5B5G] Biotin deficiency\n Def: Isolated biotin deficiency is rare. Signs of biotin deficiency in humans have been demonstrated in individuals who consume raw egg white over long periods and in total parenteral nutrition (TPN) befor...\n --PARENT--> [?] Undernutrition\n Def: Undernutrition is a condition in which the body’s requirements are unmet due to underconsumption or to impaired absorption and use of nutrients. It can be produced by lack of access to food, or as a c...\n --RELATED_TO--> [?] Fetal intrauterine malnutrition without mention of small for gestational age\n Def: Neonate, not light or small for gestational age, showing signs of fetal malnutrition, such as dry, peeling skin or loss of subcutaneous tissue....", "[4B4Y] Other specified diseases of the immune system\n --PARENT--> [04] Diseases of the immune system\n --CHILD--> [4A20] Acquired immunodeficiencies", "[4B4Y] Other specified diseases of the immune system\n --PARENT--> [04] Diseases of the immune system\n --EXCLUDES--> [?] 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....", "[5C63.Y] Other specified disorders of vitamin or non-protein cofactor absorption or transport\n --PARENT--> [5C63] Disorders of vitamin or non-protein cofactor absorption or transport\n --CHILD--> [5C63.1] Disorders of folate metabolism or transport", "[5C63.Y] Other specified disorders of vitamin or non-protein cofactor absorption or transport\n --PARENT--> [5C63] Disorders of vitamin or non-protein cofactor absorption or transport\n --CHILD--> [5C63.2] Disorders of vitamin D metabolism or transport" ]
5B5G
Biotin deficiency
[ { "from_icd11": "5B5G", "icd10_code": "E538", "icd10_title": "Deficiency of other specified B group vitamins" }, { "from_icd11": "1D45", "icd10_code": "A931", "icd10_title": "Sandfly fever" }, { "from_icd11": "PA09", "icd10_code": "V30-V39", "icd10_title": "" }, { "from_icd11": "PA09", "icd10_code": "V32", "icd10_title": "Occupant of three-wheeled motor vehicle injured in collision with two- or three-wheeled motor vehicle" }, { "from_icd11": "PA09", "icd10_code": "V329", "icd10_title": "Unspecified occupant of three-wheeled motor vehicle injured in collision with two- or three-wheeled motor vehicle in traffic accident" }, { "from_icd11": "PA09", "icd10_code": "V33", "icd10_title": "Occupant of three-wheeled motor vehicle injured in collision with car, pick-up truck or van" }, { "from_icd11": "PA09", "icd10_code": "V334", "icd10_title": "Person boarding or alighting a three-wheeled motor vehicle injured in collision with car, pick-up truck or van" }, { "from_icd11": "PA09", "icd10_code": "V335", "icd10_title": "Driver of three-wheeled motor vehicle injured in collision with car, pick-up truck or van in traffic accident" }, { "from_icd11": "PA09", "icd10_code": "V336", "icd10_title": "Passenger in three-wheeled motor vehicle injured in collision with car, pick-up truck or van in traffic accident" }, { "from_icd11": "PA09", "icd10_code": "V337", "icd10_title": "Person on outside of three-wheeled motor vehicle injured in collision with car, pick-up truck or van in traffic accident" }, { "from_icd11": "PA09", "icd10_code": "V339", "icd10_title": "Unspecified occupant of three-wheeled motor vehicle injured in collision with car, pick-up truck or van in traffic accident" }, { "from_icd11": "PA09", "icd10_code": "V34", "icd10_title": "Occupant of three-wheeled motor vehicle injured in collision with heavy transport vehicle or bus" }, { "from_icd11": "PA09", "icd10_code": "V349", "icd10_title": "Unspecified occupant of three-wheeled motor vehicle injured in collision with heavy transport vehicle or bus in traffic accident" }, { "from_icd11": "PA09", "icd10_code": "V36", "icd10_title": "Occupant of three-wheeled motor vehicle injured in collision with other nonmotor vehicle" }, { "from_icd11": "PA09", "icd10_code": "V369", "icd10_title": "Unspecified occupant of three-wheeled motor vehicle injured in collision with other nonmotor vehicle in traffic accident" } ]
E538
Deficiency of other specified B group vitamins
The mechanism of this patient’s electrolyte abnormalities is unproven, however, it most likely involves the calcium-parathyroid-vitamin D axis. Denosumab acts as a RANK-L ligand antibody, preventing osteoclast activation and the resulting bone resorption . As a result, calcium remained bound in the patient’s bones rather than in the serum, causing the parathyroid gland to respond to this perceived hypocalcemia by secreting abnormally high levels of PTH . PTH normally results in increased calcium reabsorption and phosphorus excretion by the kidneys; however, this patient also had a vitamin D deficiency, potentially secondary to elevated FGF23 and resulting inhibition of 1-alpha hydroxylase which typically activates inactive 25-OH vitamin D into active 1,25-OH vitamin D. As a result of this diminished vitamin D and decreased bone resorption, the patient was excreting phosphorus more than usual and was unable to maintain normal levels of calcium or phosphorus . This mechanism explains why repletion was initially unsuccessful as the denosumab continued to exert its effect on bone. However, as the denosumab was slowly eliminated, calcium was able to leave the bone, resulting in decreased PTH. Moreover, vitamin D repletion assisted in the reabsorption of both calcium and phosphorus by the kidneys. Therefore, the patient was successfully able to maintain the electrolyte levels with adequate repletion.
4.3125
0.752441
sec[2]/p[1]
en
0.999995
PMC8812272
https://doi.org/10.7759/cureus.20928
[ "calcium", "vitamin", "this", "bone", "phosphorus", "however", "denosumab", "resulting", "repletion", "mechanism" ]
[ { "code": "5B5K.1Z", "title": "Calcium deficiency, unspecified" }, { "code": "5B91.0", "title": "Hypercalcaemia" }, { "code": "5B5K.1Y", "title": "Other specified calcium deficiency" }, { "code": "5C64.5", "title": "Disorders of calcium metabolism" }, { "code": "FB40.Y", "title": "Other specified tenosynovitis" }, { "code": "5B7Z", "title": "Unspecified undernutrition" }, { "code": "5B90.Z", "title": "Unspecified vitamin excesses" }, { "code": "5B55.Z", "title": "Vitamin A deficiency, unspecified" }, { "code": "6C4H.1Z", "title": "Harmful pattern of use of non-psychoactive substances, unspecified" }, { "code": "5B90.Y", "title": "Other specified vitamin excess" } ]
=== ICD-11 CODES FOUND === [5B5K.1Z] Calcium deficiency, unspecified Also known as: Calcium deficiency, unspecified | Calcium deficiency | hypocalcaemia NOS | disturbance of calcium absorption | disorder of calcium absorption [5B91.0] Hypercalcaemia Definition: Hypercalcaemia is a condition caused by increased calcium levels. The higher the calcium levels and the faster its level rises, the more severe will be the symptoms. When present, symptoms are caused by dehydration secondary to urinary losses of calcium, water and other electrolytes, and to an increase in membrane potential caused by the elevation in extracellular fluid ionized calcium concentration. Patients with moderate to severe hypercalcaemia often complain of nausea and vomiting, symptoms Also known as: Hypercalcaemia | Calcium excess | elevated serum calcium | hypercalcaemic crisis | hypercalcaemic syndrome [5B5K.1Y] Other specified calcium deficiency Also known as: Other specified calcium deficiency | Dietary hypocalcaemia | dietary calcium deficiency [5C64.5] Disorders of calcium metabolism Definition: This refers to disorders in the mechanism by which the body maintains adequate calcium levels. Derangements of this mechanism lead to hypercalcaemia or hypocalcaemia, both of which can have important consequences for health. Also known as: Disorders of calcium metabolism | Calcinosis | general calcification | heterotopic calcification | metastatic calcification Excludes: Hyperparathyroidism | Chondrocalcinosis [FB40.Y] Other specified tenosynovitis Also known as: Other specified tenosynovitis | Other tenosynovitis or tendinitis | synovitis NOS | Bicipital tendinitis | biceps tendinitis [5B7Z] Unspecified undernutrition Also known as: Unspecified undernutrition | Malnutrition NOS | nutritional deficiency NOS | nutritional depletion NOS | severe malnutrition NOS [5B90.Z] Unspecified vitamin excesses Also known as: Unspecified vitamin excesses | Vitamin excesses [5B55.Z] Vitamin A deficiency, unspecified Also known as: Vitamin A deficiency, unspecified | Vitamin A deficiency | Hypovitaminosis A [6C4H.1Z] Harmful pattern of use of non-psychoactive substances, unspecified Also known as: Harmful pattern of use of non-psychoactive substances, unspecified | Harmful pattern of use of non-psychoactive substances | harmful use of nonprescribed drugs, non-dependence producing | Abuse of antacids | Abuse of herbal or folk remedies [5B90.Y] Other specified vitamin excess Also known as: Other specified vitamin excess === GRAPH WALKS === --- Walk 1 --- [5B5K.1Z] Calcium deficiency, unspecified --PARENT--> [5B5K.1] Calcium deficiency Def: Hypocalcaemia is defined as a total serum calcium concentration of less than 8.4 mg/dl (2.1 mmol/litre) or an ionized calcium concentration of less than 4.48 mg/dl (1.12 mmol/litre). There are numerou... --CHILD--> [5B5K.1Y] Other specified calcium deficiency --- Walk 2 --- [5B5K.1Z] Calcium deficiency, unspecified --PARENT--> [5B5K.1] Calcium deficiency Def: Hypocalcaemia is defined as a total serum calcium concentration of less than 8.4 mg/dl (2.1 mmol/litre) or an ionized calcium concentration of less than 4.48 mg/dl (1.12 mmol/litre). There are numerou... --RELATED_TO--> [?] Myopathy due to calcium deficiency --- Walk 3 --- [5B91.0] Hypercalcaemia Def: Hypercalcaemia is a condition caused by increased calcium levels. The higher the calcium levels and the faster its level rises, the more severe will be the symptoms. When present, symptoms are caused ... --RELATED_TO--> [?] Myopathy due to hypercalcaemia --PARENT--> [?] Hypercalcaemia Def: Hypercalcaemia is a condition caused by increased calcium levels. The higher the calcium levels and the faster its level rises, the more severe will be the symptoms. When present, symptoms are caused ... --- Walk 4 --- [5B91.0] Hypercalcaemia Def: Hypercalcaemia is a condition caused by increased calcium levels. The higher the calcium levels and the faster its level rises, the more severe will be the symptoms. When present, symptoms are caused ... --RELATED_TO--> [?] Myopathy due to hypercalcaemia --PARENT--> [?] Neurological disorders due to an excess of micro or macro nutrients --- Walk 5 --- [5B5K.1Y] Other specified calcium deficiency --PARENT--> [5B5K.1] Calcium deficiency Def: Hypocalcaemia is defined as a total serum calcium concentration of less than 8.4 mg/dl (2.1 mmol/litre) or an ionized calcium concentration of less than 4.48 mg/dl (1.12 mmol/litre). There are numerou... --RELATED_TO--> [?] Neonatal osteopenia Def: Metabolic bone disease is a common complication in very low birthweight (VLBW) preterm infants. The smallest, sickest infants are at greatest risk. Progressive osteopenia with demineralized bones and,... --- Walk 6 --- [5B5K.1Y] Other specified calcium deficiency --PARENT--> [5B5K.1] Calcium deficiency Def: Hypocalcaemia is defined as a total serum calcium concentration of less than 8.4 mg/dl (2.1 mmol/litre) or an ionized calcium concentration of less than 4.48 mg/dl (1.12 mmol/litre). There are numerou... --RELATED_TO--> [?] Neonatal hypocalcaemia Def: Hypocalcaemia is a common metabolic problem in newborns. In the neonate, hypocalcaemia is defined by birth weight (BW) categories. In infants with BW greater than 1500 g, hypocalcaemia is defined as a...
[ "[5B5K.1Z] Calcium deficiency, unspecified\n --PARENT--> [5B5K.1] Calcium deficiency\n Def: Hypocalcaemia is defined as a total serum calcium concentration of less than 8.4 mg/dl (2.1 mmol/litre) or an ionized calcium concentration of less than 4.48 mg/dl (1.12 mmol/litre). There are numerou...\n --CHILD--> [5B5K.1Y] Other specified calcium deficiency", "[5B5K.1Z] Calcium deficiency, unspecified\n --PARENT--> [5B5K.1] Calcium deficiency\n Def: Hypocalcaemia is defined as a total serum calcium concentration of less than 8.4 mg/dl (2.1 mmol/litre) or an ionized calcium concentration of less than 4.48 mg/dl (1.12 mmol/litre). There are numerou...\n --RELATED_TO--> [?] Myopathy due to calcium deficiency", "[5B91.0] Hypercalcaemia\n Def: Hypercalcaemia is a condition caused by increased calcium levels. The higher the calcium levels and the faster its level rises, the more severe will be the symptoms. When present, symptoms are caused ...\n --RELATED_TO--> [?] Myopathy due to hypercalcaemia\n --PARENT--> [?] Hypercalcaemia\n Def: Hypercalcaemia is a condition caused by increased calcium levels. The higher the calcium levels and the faster its level rises, the more severe will be the symptoms. When present, symptoms are caused ...", "[5B91.0] Hypercalcaemia\n Def: Hypercalcaemia is a condition caused by increased calcium levels. The higher the calcium levels and the faster its level rises, the more severe will be the symptoms. When present, symptoms are caused ...\n --RELATED_TO--> [?] Myopathy due to hypercalcaemia\n --PARENT--> [?] Neurological disorders due to an excess of micro or macro nutrients", "[5B5K.1Y] Other specified calcium deficiency\n --PARENT--> [5B5K.1] Calcium deficiency\n Def: Hypocalcaemia is defined as a total serum calcium concentration of less than 8.4 mg/dl (2.1 mmol/litre) or an ionized calcium concentration of less than 4.48 mg/dl (1.12 mmol/litre). There are numerou...\n --RELATED_TO--> [?] Neonatal osteopenia\n Def: Metabolic bone disease is a common complication in very low birthweight (VLBW) preterm infants. The smallest, sickest infants are at greatest risk. Progressive osteopenia with demineralized bones and,...", "[5B5K.1Y] Other specified calcium deficiency\n --PARENT--> [5B5K.1] Calcium deficiency\n Def: Hypocalcaemia is defined as a total serum calcium concentration of less than 8.4 mg/dl (2.1 mmol/litre) or an ionized calcium concentration of less than 4.48 mg/dl (1.12 mmol/litre). There are numerou...\n --RELATED_TO--> [?] Neonatal hypocalcaemia\n Def: Hypocalcaemia is a common metabolic problem in newborns. In the neonate, hypocalcaemia is defined by birth weight (BW) categories. In infants with BW greater than 1500 g, hypocalcaemia is defined as a..." ]
5B5K.1Z
Calcium deficiency, unspecified
[ { "from_icd11": "5B5K.1Z", "icd10_code": "E58", "icd10_title": "Dietary calcium deficiency" }, { "from_icd11": "5C64.5", "icd10_code": "E8352", "icd10_title": "Hypercalcemia" }, { "from_icd11": "5C64.5", "icd10_code": "E8351", "icd10_title": "Hypocalcemia" }, { "from_icd11": "5C64.5", "icd10_code": "E8359", "icd10_title": "Other disorders of calcium metabolism" }, { "from_icd11": "5C64.5", "icd10_code": "E8350", "icd10_title": "Unspecified disorder of calcium metabolism" }, { "from_icd11": "5C64.5", "icd10_code": "E835", "icd10_title": "Disorders of calcium metabolism" }, { "from_icd11": "5B7Z", "icd10_code": "E43", "icd10_title": "Unspecified severe protein-calorie malnutrition" }, { "from_icd11": "5B7Z", "icd10_code": "E538", "icd10_title": "Deficiency of other specified B group vitamins" }, { "from_icd11": "5B7Z", "icd10_code": "E569", "icd10_title": "Vitamin deficiency, unspecified" }, { "from_icd11": "5B7Z", "icd10_code": "E638", "icd10_title": "Other specified nutritional deficiencies" }, { "from_icd11": "5B7Z", "icd10_code": "E639", "icd10_title": "Nutritional deficiency, unspecified" }, { "from_icd11": "5B7Z", "icd10_code": "E41", "icd10_title": "Nutritional marasmus" }, { "from_icd11": "5B7Z", "icd10_code": "E539", "icd10_title": "Vitamin B deficiency, unspecified" }, { "from_icd11": "5B7Z", "icd10_code": "E568", "icd10_title": "Deficiency of other vitamins" }, { "from_icd11": "5B7Z", "icd10_code": "E649", "icd10_title": "Sequelae of unspecified nutritional deficiency" } ]
E58
Dietary calcium deficiency
An 81-year-old woman with a known history of hypertension and chronic obstructive pulmonary disease presented to the emergency department with unrelenting left-sided facial pain and was ultimately admitted for severe TN. Her pain had started four months ago. She described it as a stabbing sensation that started from her left ear and radiated down her left jaw and tongue. She experienced around 30 painful episodes throughout each day, with each episode lasting a few minutes. Her pain mostly occurred sporadically, but she did notice that chewing triggered the onset of her pain. She rated her pain a 10/10 during her episodes with no relieving factors. She also had associated dysphagia, generalized weakness, and a 25-pound weight loss over the past four months. She had undergone a prior MRI head with pre- and post-gadolinium-based contrast agents (GBCA) two months ago, which had not shown any significant findings. Her initial medication regimen had consisted of carbamazepine, pregabalin, and acetaminophen/codeine, which had been later switched to trials of lamotrigine, pregabalin, bupropion, and fentanyl patches. Pharmacologic therapy failed to provide any relief. Initial physical exam was significant for hypotension with systolic blood pressures in the 90s. Her labs were significant for hypokalemia (2.3 mmol/L), hypomagnesemia (1.5 mg/dL), hypoalbuminemia (2.0 g/dL), and leukocytosis (16,000/mm³).
3.884766
0.983398
sec[1]/p[0]
en
0.999998
PMC8765329
https://doi.org/10.7759/cureus.20514
[ "pain", "four", "that", "episodes", "which", "pregabalin", "known", "hypertension", "obstructive", "pulmonary" ]
[ { "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": "LD50.Y", "title": "Other specified number anomalies of chromosome X" }, { "code": "NA82.4", "title": "Multiple fractures of ribs" }, { "code": "BA4Z", "title": "Acute ischaemic heart disease, unspecified" }, { "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 === [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 [LD50.Y] Other specified number anomalies of chromosome X Also known as: Other specified number anomalies of chromosome X | Female with more than three X chromosomes | abnormal female chromosomes, with more than three x chromosomes | Tetrasomy X | 48 xxxx syndrome [NA82.4] Multiple fractures of ribs Also known as: Multiple fractures of ribs | rib fractures | Multiple rib fractures, involving first rib | Multiple rib fractures, involving two ribs | Multiple rib fractures, involving three ribs [BA4Z] Acute ischaemic heart disease, unspecified Also known as: Acute ischaemic heart disease, unspecified | acute coronary syndrome | ACS - [acute coronary syndrome] | Silent myocardial ischaemia | asymptomatic ischemia [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 --- [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 --CHILD--> [8E43.Z] Pain disorders, unspecified --- 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 --CHILD--> [8E43.Z] Pain disorders, unspecified", "[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": "NA82.4", "icd10_code": "S2249XA", "icd10_title": "Multiple fractures of ribs, unspecified side, initial encounter for closed fracture" }, { "from_icd11": "NA82.4", "icd10_code": "S2243XD", "icd10_title": "Multiple fractures of ribs, bilateral, subsequent encounter for fracture with routine healing" }, { "from_icd11": "NA82.4", "icd10_code": "S2241XS", "icd10_title": "Multiple fractures of ribs, right side, sequela" }, { "from_icd11": "NA82.4", "icd10_code": "S2249XD", "icd10_title": "Multiple fractures of ribs, unspecified side, subsequent encounter for fracture with routine healing" }, { "from_icd11": "NA82.4", "icd10_code": "S2243XS", "icd10_title": "Multiple fractures of ribs, bilateral, sequela" }, { "from_icd11": "NA82.4", "icd10_code": "S2249XS", "icd10_title": "Multiple fractures of ribs, unspecified side, sequela" } ]
R52
Pain, unspecified
On day 3, yeast-like cells grew in an aerobic blood culture bottle obtained on admission . The serum beta-D glucan measured was 10.8 pg/mL (Wako Pure Chemical Industries, Ltd., Tokyo, Japan; cut-off value, < 11 pg/mL). Retinal examination revealed no evidence of endophthalmitis. Micafungin was added at a dose of 100 mg every 24 h against suspected candidemia after an additional set of blood cultures, and the CVC was removed. The patient became afebrile after initiating systemic antifungal therapy. The colony appeared rough and pale orange in color. The colony’s India ink stain did not show a zone of clearance of ink particles, like Cryptococcus . Colonies were tested on CHROMagar Candida medium (Kanto Chemical Co., Inc., Tokyo, Japan) using matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS, the MALDI Biotyper Reference Library Ver.4.0.0.1, Filamentous Fungi Library Ver.1.0; Bruker Daltoniks, Germany), identifying them as Aureobasidium pullulans (score 1.919). On day 6, the high fever recurred. Micafungin was stopped and liposomal-amphotericin B (L-AMB) was started (3 mg/kg/day) for Cryptococcus albidus owing to a 90% probability of identification using the VITEK2 COMPACT Microbial Detection System (version 8.01 database: SYSMEX bioMerieux Co., Ltd., Tokyo, Japan). Fig. 1 Microscopy images of Aureobasidium melanigenum Gram stain of positive blood cultures
4.070313
0.94873
sec[1]/p[2]
en
0.999998
PMC8981616
https://doi.org/10.1186/s12879-022-07310-9
[ "blood", "tokyo", "japan", "like", "chemical", "micafungin", "cultures", "colony", "stain", "cryptococcus" ]
[ { "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": "1C62.Z", "title": "Human immunodeficiency virus disease without mention of tuberculosis or malaria, clinical stage unspecified" }, { "code": "1E32", "title": "Influenza, virus not identified" }, { "code": "5C56.0Y", "title": "Other specified sphingolipidosis" }, { "code": "8A44.1", "title": "Adrenoleukodystrophy" }, { "code": "4A01.31", "title": "DNA repair defects other than combined T-cell or B-cell immunodeficiencies" } ]
=== 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 [1C62.Z] Human immunodeficiency virus disease without mention of tuberculosis or malaria, clinical stage unspecified Also known as: Human immunodeficiency virus disease without mention of tuberculosis or malaria, clinical stage unspecified | Human immunodeficiency virus disease without mention of tuberculosis or malaria | human immunodeficiency virus infection | HIV - [human immunodeficiency virus infection] | HIV positive NOS [1E32] Influenza, virus not identified Definition: Any disease of the respiratory system, caused by an unidentified strain of influenza virus. These diseases are characterised by fever, cough, headache, myalgia, arthralgia, or malaise. Transmission is by inhalation of infected respiratory secretions. Also known as: Influenza, virus not identified | flu | Influenza NOS | Viral influenza specific virus not stated to have been identified | Influenza specific virus not stated to have been identified Includes: Influenza specific virus not stated to have been identified | Viral influenza specific virus not stated to have been identified Excludes: Haemophilus influenzae [H. influenzae] meningitis | Haemophilus influenzae [H. influenzae] pneumonia [5C56.0Y] Other specified sphingolipidosis Also known as: Other specified sphingolipidosis | Mucolipidosis type 4 | Sialolipidosis | Gaucher disease | Acid beta-glucosidase deficiency [8A44.1] Adrenoleukodystrophy Definition: X-linked genetic disorder associated with accumulation of very-long-chain fatty acids in the brain and adrenal cortex due to a mutation in the ABCD1 gene causing defects in peroxisomal oxidation. Neurological symptoms can present in childhood or adulthood with almost all patients having concurrent adrenal insufficiency. Also known as: Adrenoleukodystrophy | ALD - [adrenoleukodystrophy] | Addison-Schilder | Adult-onset autosomal dominant leukodystrophy | Autosomal dominant Pelizaeus-Merzbacher disease [4A01.31] DNA repair defects other than combined T-cell or B-cell immunodeficiencies Also known as: DNA repair defects other than combined T-cell or B-cell immunodeficiencies | Nijmegen breakage syndrome | Autosomal recessive nonsyndromal microcephaly with normal intelligence | Immunodeficiency - microcephaly - chromosomal instability | Microcephaly - immunodeficiency - lymphoreticuloma === 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--> [?] Diseases of spleen --- Walk 3 --- [MF50.4Z] Haematuria, unspecified --PARENT--> [MF50.4] Haematuria Def: Hematuria means presence of blood or red blood cells (RBCs) in the urine. There are two types of hematuria: gross hematuria (when one can see the blood in the urine) and microscopic hematuria (when th... --CHILD--> [MF50.40] 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... --EXCLUDES--> [?] Recurrent or persistent glomerular haematuria Def: The presence in the urine of glomerular origin red blood cells (RBCs). In microscopic haematuria the urine appears normal to the naked eye, but examination with a microscope shows a high number of RBC... --- Walk 5 --- [MA12.1] Finding of cocaine in blood --PARENT--> [MA12] Clinical findings of drugs, medicaments and biological substances in blood, blood-forming organs, or the immune system --PARENT--> [?] Clinical findings in blood, blood-forming organs, or the immune system --- Walk 6 --- [MA12.1] Finding of cocaine in blood --PARENT--> [MA12] Clinical findings of drugs, medicaments and biological substances in blood, blood-forming organs, or the immune system --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--> [?] Diseases of spleen", "[MF50.4Z] Haematuria, unspecified\n --PARENT--> [MF50.4] Haematuria\n Def: Hematuria means presence of blood or red blood cells (RBCs) in the urine. There are two types of hematuria: gross hematuria (when one can see the blood in the urine) and microscopic hematuria (when th...\n --CHILD--> [MF50.40] 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 --EXCLUDES--> [?] Recurrent or persistent glomerular haematuria\n Def: The presence in the urine of glomerular origin red blood cells (RBCs). In microscopic haematuria the urine appears normal to the naked eye, but examination with a microscope shows a high number of RBC...", "[MA12.1] Finding of cocaine in blood\n --PARENT--> [MA12] Clinical findings of drugs, medicaments and biological substances in blood, blood-forming organs, or the immune system\n --PARENT--> [?] Clinical findings in blood, blood-forming organs, or the immune system", "[MA12.1] Finding of cocaine in blood\n --PARENT--> [MA12] Clinical findings of drugs, medicaments and biological substances in blood, blood-forming organs, or the immune system\n --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
ECG revealed normal sinus rhythm with Q waves in leads II, III, and aVF, and ST segment depression in V5-V6 . Chest radiography and CT revealed a CTR of 72% and severe calcified coronary arteries . UCG revealed poor left ventricular function (LVDd/Ds, 56/43 mm; LVEF, 44%; inferoposterior wall hypokinesis; and mild MR with RVP of 29 mmHg). Cineangiography 4 years ago had shown only 25% stenosis in the proximal LAD; at admission, it revealed 90% stenosis in the same proximal LAD, 99% stenosis in the proximal LCX, and 95% stenosis in the posterolateral branch (PL) of LCX . He had low blood pressure during dialysis and underwent emergency surgery (Euro II risk score 40.7%; STS risk score, 33.2%). Fig. 4 Preoperative electrocardiogram in Case 2. Electrocardiogram (ECG) showing normal sinus rhythm with Q waves in leads II, III, and aVF, and ST segment depression in V5-V6 Fig. 5 Preoperative chest radiography and computed tomography in Case 2. Chest radiography and computed tomography (CT) showing a CTR of 72% and severely calcified coronary arteries Fig. 6 Coronary angiogram in Case 2. a Four years previously. A right coronary artery hypoplastic artery with no stenosis in the left anterior descending artery (LAD) and left circumflex artery (LCX). b At admission. The images show 90% stenosis in the proximal LAD, 99% stenosis in the proximal LCX, and 90% stenosis in the posterolateral branch of the LCX
3.984375
0.944336
sec[1]/sec[1]/p[2]
en
0.999998
34082711
https://doi.org/10.1186/s12872-021-02076-5
[ "stenosis", "coronary", "artery", "chest", "radiography", "sinus", "rhythm", "waves", "leads", "segment" ]
[ { "code": "DB30.Y", "title": "Other specified obstruction of large intestine" }, { "code": "BB60.Z", "title": "Mitral valve stenosis, unspecified" }, { "code": "BD52.2", "title": "Stricture of artery" }, { "code": "FA82", "title": "Spinal stenosis" }, { "code": "DA40.0", "title": "Gastric outlet obstruction" }, { "code": "BA8Z", "title": "Diseases of coronary artery, unspecified" }, { "code": "BA4Z", "title": "Acute ischaemic heart disease, unspecified" }, { "code": "BA41.Z", "title": "Acute myocardial infarction, unspecified" }, { "code": "BA5Z", "title": "Chronic ischaemic heart disease, unspecified" }, { "code": "LA8C.2", "title": "Congenital coronary arterial fistula" } ]
=== ICD-11 CODES FOUND === [DB30.Y] Other specified obstruction of large intestine Also known as: Other specified obstruction of large intestine | Obstruction of large intestine due to compression or stenosis | Acute bowel obstruction, not elsewhere classified | Subacute bowel obstruction, not elsewhere classified | subacute intestinal obstruction NOS [BB60.Z] Mitral valve stenosis, unspecified Also known as: Mitral valve stenosis, unspecified | Mitral valve stenosis | MS - [mitral stenosis] | mitral stenosis | mitral valvular stricture [BD52.2] Stricture of artery Also known as: Stricture of artery | arterial stenosis | arterial stricture | artery stricture | stenosis of artery [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 [DA40.0] Gastric outlet obstruction Definition: Gastric outlet obstruction is a disorder characterised by epigastric abdominal pain and postprandial vomiting due to mechanical obstruction mostly at the level of the pylorus. Also known as: Gastric outlet obstruction | Adult hypertrophic pyloric stenosis | gastric outflow obstruction | hypertrophic pylorus stenosis | hypertrophic pylorus stricture [BA8Z] Diseases of coronary artery, unspecified Also known as: Diseases of coronary artery, unspecified | coronary artery insufficiency | coronary artery heart disease | CAD - [coronary artery disease] | coronary artery disorder [BA4Z] Acute ischaemic heart disease, unspecified Also known as: Acute ischaemic heart disease, unspecified | acute coronary syndrome | ACS - [acute coronary syndrome] | Silent myocardial ischaemia | asymptomatic ischemia [BA41.Z] Acute myocardial infarction, unspecified Also known as: Acute myocardial infarction, unspecified | Acute myocardial infarction | cardiac attack | heart attack | acute cardiac infarction [BA5Z] Chronic ischaemic heart disease, unspecified Also known as: Chronic ischaemic heart disease, unspecified | Ischaemic heart disease (chronic) NOS | coronary ischaemia | coronary damage NOS | atheroma of heart [LA8C.2] Congenital coronary arterial fistula Definition: A congenital cardiovascular malformation in which a coronary artery communicates, through an anomalous channel, with a cardiac chamber or with any segment of the systemic or pulmonary circulation. Additional information: this communication may be simple and direct or may be tortuous and dilated. In order of frequency the involved coronary artery is the right, the left and, rarely, both coronary arteries. Occasionally multiple fistulas are present. Also known as: Congenital coronary arterial fistula | coronary fistula | congenital arteriovenous coronary fistula | congenital coronary fistula to pulmonary artery | Congenital coronary arterial fistula to right ventricle Includes: congenital coronary fistula to pulmonary artery Excludes: anomalous origin of coronary artery from pulmonary arterial tree === GRAPH WALKS === --- Walk 1 --- [DB30.Y] Other specified obstruction of large intestine --PARENT--> [DB30] Obstruction of large intestine Def: Hindrance of the passage of luminal contents in the large intestine. Obstruction of the large intestine can be partial or complete, and caused by intrinsic or extrinsic factors. Simple obstruction is ... --EXCLUDES--> [?] Paralytic ileus of large intestine Def: Paralytic ileus of large intestine is a decreased motor activity of colon due to non-mechanical causes. The intestinal paralysis need not be complete, but it must be sufficient to prohibit the passage... --- Walk 2 --- [DB30.Y] Other specified obstruction of large intestine --PARENT--> [DB30] Obstruction of large intestine Def: Hindrance of the passage of luminal contents in the large intestine. Obstruction of the large intestine can be partial or complete, and caused by intrinsic or extrinsic factors. Simple obstruction is ... --CHILD--> [DB30.0] Intussusception of the large intestine Def: Intussusception occurs when a segment of bowel invaginatetes, or telescopeds, into adjacent distal bowel, leading to obstruction and possibly ischemic injury. Colonic intussusception is a relatively u... --- Walk 3 --- [BB60.Z] Mitral valve stenosis, unspecified --PARENT--> [BB60] Mitral valve stenosis --EXCLUDES--> [?] Mitral valve stenosis with insufficiency Def: This is a valvular heart disease characterised by the narrowing of the orifice of the mitral valve of the heart, with regurgitation.... --- Walk 4 --- [BB60.Z] Mitral valve stenosis, unspecified --PARENT--> [BB60] Mitral valve stenosis --CHILD--> [BB60.Z] Mitral valve stenosis, unspecified --- Walk 5 --- [BD52.2] Stricture of artery --PARENT--> [BD52] Certain specified disorders of arteries or arterioles --PARENT--> [?] Diseases of arteries or arterioles --- Walk 6 --- [BD52.2] Stricture of artery --PARENT--> [BD52] Certain specified disorders of arteries or arterioles --CHILD--> [BD52.2] Stricture of artery
[ "[DB30.Y] Other specified obstruction of large intestine\n --PARENT--> [DB30] Obstruction of large intestine\n Def: Hindrance of the passage of luminal contents in the large intestine. Obstruction of the large intestine can be partial or complete, and caused by intrinsic or extrinsic factors. Simple obstruction is ...\n --EXCLUDES--> [?] Paralytic ileus of large intestine\n Def: Paralytic ileus of large intestine is a decreased motor activity of colon due to non-mechanical causes. The intestinal paralysis need not be complete, but it must be sufficient to prohibit the passage...", "[DB30.Y] Other specified obstruction of large intestine\n --PARENT--> [DB30] Obstruction of large intestine\n Def: Hindrance of the passage of luminal contents in the large intestine. Obstruction of the large intestine can be partial or complete, and caused by intrinsic or extrinsic factors. Simple obstruction is ...\n --CHILD--> [DB30.0] Intussusception of the large intestine\n Def: Intussusception occurs when a segment of bowel invaginatetes, or telescopeds, into adjacent distal bowel, leading to obstruction and possibly ischemic injury. Colonic intussusception is a relatively u...", "[BB60.Z] Mitral valve stenosis, unspecified\n --PARENT--> [BB60] Mitral valve stenosis\n --EXCLUDES--> [?] Mitral valve stenosis with insufficiency\n Def: This is a valvular heart disease characterised by the narrowing of the orifice of the mitral valve of the heart, with regurgitation....", "[BB60.Z] Mitral valve stenosis, unspecified\n --PARENT--> [BB60] Mitral valve stenosis\n --CHILD--> [BB60.Z] Mitral valve stenosis, unspecified", "[BD52.2] Stricture of artery\n --PARENT--> [BD52] Certain specified disorders of arteries or arterioles\n --PARENT--> [?] Diseases of arteries or arterioles", "[BD52.2] Stricture of artery\n --PARENT--> [BD52] Certain specified disorders of arteries or arterioles\n --CHILD--> [BD52.2] Stricture of artery" ]
DB30.Y
Other specified obstruction of large intestine
[ { "from_icd11": "BB60.Z", "icd10_code": "I050", "icd10_title": "Rheumatic mitral stenosis" }, { "from_icd11": "BB60.Z", "icd10_code": "I342", "icd10_title": "Nonrheumatic mitral (valve) stenosis" }, { "from_icd11": "BD52.2", "icd10_code": "I771", "icd10_title": "Stricture of artery" }, { "from_icd11": "FA82", "icd10_code": "M48061", "icd10_title": "Spinal stenosis, lumbar region without neurogenic claudication" }, { "from_icd11": "FA82", "icd10_code": "M4800", "icd10_title": "Spinal stenosis, site unspecified" }, { "from_icd11": "FA82", "icd10_code": "M4806", "icd10_title": "Spinal stenosis, lumbar region" }, { "from_icd11": "FA82", "icd10_code": "M4807", "icd10_title": "Spinal stenosis, lumbosacral region" }, { "from_icd11": "FA82", "icd10_code": "M4804", "icd10_title": "Spinal stenosis, thoracic region" }, { "from_icd11": "FA82", "icd10_code": "M48062", "icd10_title": "Spinal stenosis, lumbar region with neurogenic claudication" }, { "from_icd11": "FA82", "icd10_code": "M4808", "icd10_title": "Spinal stenosis, sacral and sacrococcygeal region" }, { "from_icd11": "FA82", "icd10_code": "M4805", "icd10_title": "Spinal stenosis, thoracolumbar region" }, { "from_icd11": "FA82", "icd10_code": "M4803", "icd10_title": "Spinal stenosis, cervicothoracic region" }, { "from_icd11": "FA82", "icd10_code": "M4801", "icd10_title": "Spinal stenosis, occipito-atlanto-axial region" }, { "from_icd11": "FA82", "icd10_code": "M480", "icd10_title": "Spinal stenosis" }, { "from_icd11": "DA40.0", "icd10_code": "K311", "icd10_title": "Adult hypertrophic pyloric stenosis" } ]
I050
Rheumatic mitral stenosis
Both leprosy and syphilis were considered in the clinical differential diagnosis of our patient’s infiltrative plaques. However, leprosy and syphilis may present a challenging differential diagnosis . Both diseases have polymorphous presentations and occasionally present unclear laboratory tests which hinder definitive clinical diagnosis of the presenting lesions . Syphilis,” the great imitator” , normally presents as a papulo-squamous rash, but in HIV positive patients it may present atypically as annular, nodular or granulomatous plaques . In fact, nodular and granulomatous syphilis has occasionally been clinically and/or histopathologically misdiagnosed as indeterminate or tuberculoid or borderline lepromatous leprosy especially in HIV infected patients . Given the aforementioned confusion in earlier cases even on histology, the weakly reactive RPR result and the initial improvement on ceftriaxone and doxycycline, syphilitic palmar keratoderma and ocular lesions remained a possible diagnosis in our patient. The initial improvement following the institution of ceftriaxone and doxycycline for the suspected syphilis was probably just due to rifampicin monotherapy for leprosy whilst the patient was receiving PTB treatment from his base hospital. Whilst this regimen is effective for early syphilis , it is not effective for leprosy. Of the tetracyclines, only minocycline is effective for leprosy .
4.1875
0.902832
sec[2]/p[1]
en
0.999998
34193098
https://doi.org/10.1186/s12890-021-01572-w
[ "leprosy", "syphilis", "present", "effective", "both", "differential", "plaques", "occasionally", "lesions", "patients" ]
[ { "code": "1B20.Z", "title": "Leprosy, unspecified" }, { "code": "1B20.3", "title": "Complications of leprosy" }, { "code": "1B20.2", "title": "Leprosy reactions" }, { "code": "8D83", "title": "Autonomic nervous system disorder due to infection" }, { "code": "1B20.0", "title": "Paucibacillary leprosy" }, { "code": "1A6Z", "title": "Syphilis, unspecified" }, { "code": "1A60.Z", "title": "Congenital syphilis, unspecified" }, { "code": "1A61.0", "title": "Primary genital syphilis" }, { "code": "1A61.Z", "title": "Early syphilis, unspecified" }, { "code": "QC90.2", "title": "Contact with or exposure to infections with a predominantly sexual mode of transmission" } ]
=== ICD-11 CODES FOUND === [1B20.Z] Leprosy, unspecified Also known as: Leprosy, unspecified | Leprosy | Hansen disease | Infection due to Mycobacterium leprae | anaesthesia leprosy [1B20.3] Complications of leprosy Also known as: Complications of leprosy | Arthritis due to leprosy | Polyneuropathy due to leprosy | Involvement of eyelid in leprosy | Neuropathic skin ulceration due to leprosy [1B20.2] Leprosy reactions Also known as: Leprosy reactions [8D83] Autonomic nervous system disorder due to infection Also known as: Autonomic nervous system disorder due to infection | Autonomic disorder due to Botulism | Autonomic disorder due to certain specified infection | Autonomic disorder due to Chagas disease | Autonomic disorder due to Diphtheria [1B20.0] Paucibacillary leprosy Also known as: Paucibacillary leprosy | Hansen disease, paucibacillary | Indeterminate leprosy | Hansen disease, indeterminate | Indeterminate macular leprosy [1A6Z] Syphilis, unspecified Also known as: Syphilis, unspecified | Lues | luetic disease | syphilis NOS | Interstitial keratitis and keratoconjunctivitis in syphilis [1A60.Z] Congenital syphilis, unspecified Also known as: Congenital syphilis, unspecified | Congenital syphilis | congenital syphilis, unspecified | hereditary syphilis | heredosyphilis [1A61.0] Primary genital syphilis Definition: A disease caused by an infection with the gram-negative bacteria Treponema pallidum pallidum. This disease is characterised by a single chancre in the genital region. Transmission is commonly by sexual contact. Also known as: Primary genital syphilis | Genital syphilitic chancre | genital chancre | genital syphilis | chancre [1A61.Z] Early syphilis, unspecified Also known as: Early syphilis, unspecified | Early syphilis | syphilis causing death under 2 years of age, stated to be acquired | early syphilis, unspecified | acquired syphilis [QC90.2] Contact with or exposure to infections with a predominantly sexual mode of transmission Also known as: Contact with or exposure to infections with a predominantly sexual mode of transmission | exposure to sexually transmitted disease | suspected contact with or exposure to infections with a predominantly sexual mode of transmission | contact with sexually transmitted communicable disease | contact with sexually transmitted disease === GRAPH WALKS === --- Walk 1 --- [1B20.Z] Leprosy, unspecified --PARENT--> [1B20] Leprosy Def: A disease caused by an infection with Mycobacterium leprae. This disease commonly presents with a long asymptomatic period followed by granulomatous lesions of the skin, respiratory tract, and periphe... --CHILD--> [1B20.0] Paucibacillary leprosy --- Walk 2 --- [1B20.Z] Leprosy, unspecified --PARENT--> [1B20] Leprosy Def: A disease caused by an infection with Mycobacterium leprae. This disease commonly presents with a long asymptomatic period followed by granulomatous lesions of the skin, respiratory tract, and periphe... --CHILD--> [1B20.0] Paucibacillary leprosy --- Walk 3 --- [1B20.3] Complications of leprosy --PARENT--> [1B20] Leprosy Def: A disease caused by an infection with Mycobacterium leprae. This disease commonly presents with a long asymptomatic period followed by granulomatous lesions of the skin, respiratory tract, and periphe... --CHILD--> [1B20.0] Paucibacillary leprosy --- Walk 4 --- [1B20.3] Complications of leprosy --PARENT--> [1B20] Leprosy Def: A disease caused by an infection with Mycobacterium leprae. This disease commonly presents with a long asymptomatic period followed by granulomatous lesions of the skin, respiratory tract, and periphe... --CHILD--> [1B20.2] Leprosy reactions --- Walk 5 --- [1B20.2] Leprosy reactions --CHILD--> [1B20.21] Type II leprosy reaction Def: This phenomenon, also named downgrading reaction, occurs in borderline leprosy states and is associated with a decrease in cell-mediated immunity with a shift towards the lepromatous end of the clinic... --PARENT--> [1B20.2] Leprosy reactions --- Walk 6 --- [1B20.2] Leprosy reactions --PARENT--> [1B20] Leprosy Def: A disease caused by an infection with Mycobacterium leprae. This disease commonly presents with a long asymptomatic period followed by granulomatous lesions of the skin, respiratory tract, and periphe... --CHILD--> [1B20.1] Multibacillary leprosy
[ "[1B20.Z] Leprosy, unspecified\n --PARENT--> [1B20] Leprosy\n Def: A disease caused by an infection with Mycobacterium leprae. This disease commonly presents with a long asymptomatic period followed by granulomatous lesions of the skin, respiratory tract, and periphe...\n --CHILD--> [1B20.0] Paucibacillary leprosy", "[1B20.Z] Leprosy, unspecified\n --PARENT--> [1B20] Leprosy\n Def: A disease caused by an infection with Mycobacterium leprae. This disease commonly presents with a long asymptomatic period followed by granulomatous lesions of the skin, respiratory tract, and periphe...\n --CHILD--> [1B20.0] Paucibacillary leprosy", "[1B20.3] Complications of leprosy\n --PARENT--> [1B20] Leprosy\n Def: A disease caused by an infection with Mycobacterium leprae. This disease commonly presents with a long asymptomatic period followed by granulomatous lesions of the skin, respiratory tract, and periphe...\n --CHILD--> [1B20.0] Paucibacillary leprosy", "[1B20.3] Complications of leprosy\n --PARENT--> [1B20] Leprosy\n Def: A disease caused by an infection with Mycobacterium leprae. This disease commonly presents with a long asymptomatic period followed by granulomatous lesions of the skin, respiratory tract, and periphe...\n --CHILD--> [1B20.2] Leprosy reactions", "[1B20.2] Leprosy reactions\n --CHILD--> [1B20.21] Type II leprosy reaction\n Def: This phenomenon, also named downgrading reaction, occurs in borderline leprosy states and is associated with a decrease in cell-mediated immunity with a shift towards the lepromatous end of the clinic...\n --PARENT--> [1B20.2] Leprosy reactions", "[1B20.2] Leprosy reactions\n --PARENT--> [1B20] Leprosy\n Def: A disease caused by an infection with Mycobacterium leprae. This disease commonly presents with a long asymptomatic period followed by granulomatous lesions of the skin, respiratory tract, and periphe...\n --CHILD--> [1B20.1] Multibacillary leprosy" ]
1B20.Z
Leprosy, unspecified
[ { "from_icd11": "1B20.Z", "icd10_code": "A309", "icd10_title": "Leprosy, unspecified" }, { "from_icd11": "1B20.Z", "icd10_code": "A30-A49", "icd10_title": "" }, { "from_icd11": "1B20.Z", "icd10_code": "A30", "icd10_title": "Leprosy [Hansen's disease]" }, { "from_icd11": "1B20.Z", "icd10_code": "A308", "icd10_title": "Other forms of leprosy" }, { "from_icd11": "1B20.0", "icd10_code": "A300", "icd10_title": "Indeterminate leprosy" }, { "from_icd11": "1B20.0", "icd10_code": "A301", "icd10_title": "Tuberculoid leprosy" }, { "from_icd11": "1B20.0", "icd10_code": "A302", "icd10_title": "Borderline tuberculoid leprosy" }, { "from_icd11": "1A6Z", "icd10_code": "A539", "icd10_title": "Syphilis, unspecified" }, { "from_icd11": "1A6Z", "icd10_code": "A53", "icd10_title": "Other and unspecified syphilis" }, { "from_icd11": "1A6Z", "icd10_code": "M031", "icd10_title": "" }, { "from_icd11": "1A6Z", "icd10_code": "K672", "icd10_title": "" }, { "from_icd11": "1A60.Z", "icd10_code": "A509", "icd10_title": "Congenital syphilis, unspecified" }, { "from_icd11": "1A60.Z", "icd10_code": "A50", "icd10_title": "Congenital syphilis" }, { "from_icd11": "1A60.Z", "icd10_code": "A502", "icd10_title": "Early congenital syphilis, unspecified" }, { "from_icd11": "1A60.Z", "icd10_code": "A507", "icd10_title": "Late congenital syphilis, unspecified" } ]
A309
Leprosy, unspecified
Metastasis of the tumor to the calvarium can occur in several cancers, most frequently originating from the prostate, breast, thyroid, and lung. Bladder carcinoma typically spreads to the bone marrow, liver, and lungs. However, skull metastasis from urothelial carcinoma of the urinary bladder (UCB) is rare, occurring in less than 1.0% of patients with this condition. When distant metastasis occurs, the prognosis becomes poor. A solid mass causing lytic lesions in the skull indicates metastasis and can present with a range of imaging findings. Metastasis to the skull can lead to numerous clinical symptoms, like local swelling, ulceration of skin, cosmetic issues, pain, bleeding, dural sinus compression, neurological deficits, and sinus thrombosis. Metastasis to the bone significantly deteriorates the prognosis for cancer patients due to the progression of the primary cancer or organ infiltration. If metastases to the cranium invade or overlie the dural venous sinus, resecting them surgically can offer effective palliation for symptomatic calvarial metastasis. Additionally, focal palliative radiotherapy can help relieve symptoms and prevent recurrence . One of the key goals in staging the tumor is to determine whether it has invaded the muscle, as this significantly affects the prognosis and management. We present a patient who is a middle-aged woman with calvarial metastasis from bladder cancer.
4.140625
0.937012
sec[0]/p[1]
en
0.999999
PMC11282353
https://doi.org/10.7759/cureus.63171
[ "metastasis", "bladder", "skull", "prognosis", "sinus", "cancer", "tumor", "carcinoma", "bone", "patients" ]
[ { "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": "GC01.Z", "title": "Disorder of bladder, unspecified" }, { "code": "GC00.1", "title": "Infectious cystitis" }, { "code": "GC01.0", "title": "Bladder neck obstruction" }, { "code": "GC01.Y", "title": "Other specified disorders of bladder" }, { "code": "QF01.Y", "title": "Other specified acquired absence of organs" } ]
=== 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 [GC01.Z] Disorder of bladder, unspecified Also known as: Disorder of bladder, unspecified | Other disorders of bladder [GC00.1] Infectious cystitis Definition: Inflammation of the urinary bladder caused by microbes Also known as: Infectious cystitis | inflammation of bladder | suppuration bladder | infective cystitis | infection of bladder Excludes: tuberculous cystitis (NHEA) | bladder disorder in schistosomiasis [bilharziasis] (NHEB) [GC01.0] Bladder neck obstruction Definition: A condition of the bladder, caused by congenital or acquired abnormalities that impair the muscles that connect the bladder to the urethra. This condition is characterised by obstruction of the bladder neck and constricted opening during urination. This condition may also present with pelvic pain, pollakiuria, incontinence, or incomplete bladder emptying. Confirmation is by video urodynamics to observe the obstruction as the bladder fills and voids. Also known as: Bladder neck obstruction | bladder outlet obstruction | obstruction of bladder neck or vesicourethral orifice | vesicourethral orifice obstruction | BNO - [bladder neck obstruction] Includes: Acquired bladder neck stenosis [GC01.Y] Other specified disorders of bladder Also known as: Other specified disorders of bladder | Non-neurogenic neurogenic bladder | Occult neuropathic bladder | Hinman syndrome | Hinman-Allen syndrome [QF01.Y] Other specified acquired absence of organs Also known as: Other specified acquired absence of organs | Acquired absence of part of head or neck | Acquired absence of eye | absence of eye | absence of eyeball === GRAPH WALKS === --- Walk 1 --- [2E2Z] Malignant neoplasm metastasis, unspecified --PARENT--> [?] Malignant neoplasm metastases Def: Spread of a malignant neoplasm into secondary sites.... --CHILD--> [2D51] Malignant neoplasm metastasis in meninges --- Walk 2 --- [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 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 --PARENT--> [?] Malignant neoplasm metastases Def: Spread of a malignant neoplasm into secondary sites.... --- 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 --PARENT--> [?] Malignant neoplasm metastases Def: Spread of a malignant neoplasm into secondary sites.... --- 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 --PARENT--> [?] Malignant neoplasm metastases Def: Spread of a malignant neoplasm into secondary sites....
[ "[2E2Z] Malignant neoplasm metastasis, unspecified\n --PARENT--> [?] Malignant neoplasm metastases\n Def: Spread of a malignant neoplasm into secondary sites....\n --CHILD--> [2D51] Malignant neoplasm metastasis in meninges", "[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", "[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 --PARENT--> [?] Malignant neoplasm metastases\n Def: Spread of a malignant neoplasm into secondary sites....", "[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 --PARENT--> [?] Malignant neoplasm metastases\n Def: Spread of a malignant neoplasm into secondary sites....", "[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 --PARENT--> [?] Malignant neoplasm metastases\n Def: Spread of a malignant neoplasm into secondary sites...." ]
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": "GC01.Z", "icd10_code": "N3289", "icd10_title": "Other specified disorders of bladder" } ]
C7949
Secondary malignant neoplasm of other parts of nervous system
These nodules often require lung segmentectomy, even combined segmentectomy. We can perform 3D reconstruction of the lobes, bronchial vessels, and other anatomic structures to simulate segmentectomy preoperatively. Localisation by 3D-CTLR allows identification of safe surgical margins, especially for lung nodules located in the plane between segments or subsegments, and then allows the anatomic resection of the targeted segment to be minimised while meeting oncologic requirements . Fig. 6 Illustration of the localisation procedure in patient 5. A A computed tomography image showing a nodule (yellow arrow) in the right upper lobe. B Three-dimensional computed tomography lung reconstruction showing that the nodule is located in the upper lobe of the right lung, far from the pleura, but that the projection position of the nodule on the lung surface is approximately the middle of the upper and lower boundaries. Three-dimensional computed tomography bronchography and angiography suggest that the nodules are located at the apical segment of the right upper lobe but close to the posterior segment. C Localisation is based on the distance between the nodule and the upper and lower boundaries and a burn mark made with an electrotome. D The resected specimen after apical segmentectomy shows adequate surgical margins (arrow). The final histology confirmed this lesion to be minimally invasive adenocarcinoma
4.015625
0.555176
sec[1]/sec[1]/sec[1]/p[0]
en
0.999999
34565436
https://doi.org/10.1186/s13019-021-01666-w
[ "lung", "segmentectomy", "nodule", "nodules", "localisation", "located", "segment", "computed", "tomography", "lobe" ]
[ { "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": "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 === [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 [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 --- [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 2 --- [CB40.Y] Other specified diseases of the respiratory system --PARENT--> [CB40] Certain diseases of the respiratory system --CHILD--> [CB40.2] Pulmonary collapse --- Walk 3 --- [LA75.1] Agenesis of lung Def: This refers to the absence or rudimentary residua of an undeveloped lung.... --PARENT--> [LA75] Structural developmental anomalies of lungs Def: Any condition caused by failure of the lungs to correctly develop during the antenatal period.... --CHILD--> [LA75.0] Accessory lobe of lung Def: An extra lobe of lung beyond the 3 on the right and the 2 on the left... --- Walk 4 --- [LA75.1] Agenesis of lung Def: This refers to the absence or rudimentary residua of an undeveloped lung.... --PARENT--> [LA75] Structural developmental anomalies of lungs Def: Any condition caused by failure of the lungs to correctly develop during the antenatal period.... --CHILD--> [LA75.0] Accessory lobe of lung Def: An extra lobe of lung beyond the 3 on the right and the 2 on the left... --- Walk 5 --- [CA40.Z] Pneumonia, organism unspecified --PARENT--> [CA40] Pneumonia Def: A disease of the lungs, frequently but not always caused by an infection with bacteria, virus, fungus, or parasite. This disease is characterised by fever, chills, cough with sputum production, chest ... --RELATED_TO--> [?] Severe acute respiratory syndrome Def: A disease of the respiratory system, caused by an infection with coronavirus. This disease is characterised by fever, headache, cough, myalgia, tachycardia, or diarrhoea. This disease may also lead to... --- Walk 6 --- [CA40.Z] Pneumonia, organism unspecified --PARENT--> [CA40] Pneumonia Def: A disease of the lungs, frequently but not always caused by an infection with bacteria, virus, fungus, or parasite. This disease is characterised by fever, chills, cough with sputum production, chest ... --CHILD--> [CA40.1] Viral pneumonia Def: A disease of the pulmonary system, caused by an infection with a viral source. This disease is characterised by fever, lethargy, headache, myalgia, vomiting, or coughing. Transmission is by inhalation...
[ "[CB40.Y] Other specified diseases of the respiratory system\n --PARENT--> [CB40] Certain diseases of the respiratory system\n --RELATED_TO--> [?] 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 --CHILD--> [CB40.2] Pulmonary collapse", "[LA75.1] Agenesis of lung\n Def: This refers to the absence or rudimentary residua of an undeveloped lung....\n --PARENT--> [LA75] Structural developmental anomalies of lungs\n Def: Any condition caused by failure of the lungs to correctly develop during the antenatal period....\n --CHILD--> [LA75.0] Accessory lobe of lung\n Def: An extra lobe of lung beyond the 3 on the right and the 2 on the left...", "[LA75.1] Agenesis of lung\n Def: This refers to the absence or rudimentary residua of an undeveloped lung....\n --PARENT--> [LA75] Structural developmental anomalies of lungs\n Def: Any condition caused by failure of the lungs to correctly develop during the antenatal period....\n --CHILD--> [LA75.0] Accessory lobe of lung\n Def: An extra lobe of lung beyond the 3 on the right and the 2 on the left...", "[CA40.Z] Pneumonia, organism unspecified\n --PARENT--> [CA40] Pneumonia\n Def: A disease of the lungs, frequently but not always caused by an infection with bacteria, virus, fungus, or parasite. This disease is characterised by fever, chills, cough with sputum production, chest ...\n --RELATED_TO--> [?] 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...", "[CA40.Z] Pneumonia, organism unspecified\n --PARENT--> [CA40] Pneumonia\n Def: A disease of the lungs, frequently but not always caused by an infection with bacteria, virus, fungus, or parasite. This disease is characterised by fever, chills, cough with sputum production, chest ...\n --CHILD--> [CA40.1] Viral pneumonia\n Def: A disease of the pulmonary system, caused by an infection with a viral source. This disease is characterised by fever, lethargy, headache, myalgia, vomiting, or coughing. Transmission is by inhalation..." ]
CB40.Y
Other specified diseases of the respiratory system
[ { "from_icd11": "LA75.1", "icd10_code": "Q333", "icd10_title": "Agenesis of lung" }, { "from_icd11": "CA40.Z", "icd10_code": "J189", "icd10_title": "Pneumonia, unspecified organism" }, { "from_icd11": "CA40.Z", "icd10_code": "J181", "icd10_title": "Lobar pneumonia, unspecified organism" }, { "from_icd11": "CA40.Z", "icd10_code": "J188", "icd10_title": "Other pneumonia, unspecified organism" }, { "from_icd11": "CA40.Z", "icd10_code": "J168", "icd10_title": "Pneumonia due to other specified infectious organisms" }, { "from_icd11": "CA40.Z", "icd10_code": "J180", "icd10_title": "Bronchopneumonia, unspecified organism" }, { "from_icd11": "CA40.Z", "icd10_code": "J17", "icd10_title": "Pneumonia in diseases classified elsewhere" }, { "from_icd11": "CA40.Z", "icd10_code": "J182", "icd10_title": "Hypostatic pneumonia, unspecified organism" }, { "from_icd11": "CA40.Z", "icd10_code": "J16", "icd10_title": "Pneumonia due to other infectious organisms, not elsewhere classified" }, { "from_icd11": "CA40.Z", "icd10_code": "J171", "icd10_title": "" }, { "from_icd11": "CA40.Z", "icd10_code": "J173", "icd10_title": "" }, { "from_icd11": "CA40.Z", "icd10_code": "J178", "icd10_title": "" }, { "from_icd11": "CA40.Z", "icd10_code": "J18", "icd10_title": "Pneumonia, unspecified organism" }, { "from_icd11": "CB41", "icd10_code": "J9622", "icd10_title": "Acute and chronic respiratory failure with hypercapnia" }, { "from_icd11": "CB41", "icd10_code": "J9620", "icd10_title": "Acute and chronic respiratory failure, unspecified whether with hypoxia or hypercapnia" } ]
Q333
Agenesis of lung
Here, we present a child with an epileptic encephalopathy resulting from a homozygous variant in the CAD gene (c.98T > G.p.Met33Arg) whose seizures resolved and encephalopathy improved with TAU treatment. There is a growing body of work demonstrating that refractory epilepsy and encephalopathy are frequently encountered in patients with inborn errors of metabolism. 9 , 10 Furthermore, the effectiveness of therapies that are targeted to specific metabolic pathways has been well‐documented. 11 , 12 , 13 For example, Hunt et al. documented a case of neonatal epilepsy resolved by daily pyridoxine treatment, with genetic studies in the past 2 decades highlighting the involvement of ALDH7A1 and PROSC in pyridoxine‐dependent epilepsy. 14 , 15 Since then, various metabolic pathways involving biotin recycling, glucose transport, creatine synthesis, purine metabolism, and Coenzyme Q10 deficiency have been implicated in pediatric epilepsy syndromes, with substantial response to replacement therapies. 9 The success of uridine supplementation in the treatment of several cases of epileptic encephalopathy resulting from CAD mutations further demonstrates the impact of genetic‐based epilepsy therapies. Exome sequencing as well as targeted gene panels have been shown to play an increasingly important role in elucidating these rare and often de novo genetic variants underlying epileptic encephalopathies. 16 , 17
4.367188
0.689941
sec[3]/p[0]
en
0.999998
33249780
https://doi.org/10.1002/acn3.51257
[ "epilepsy", "encephalopathy", "epileptic", "therapies", "genetic", "resulting", "gene", "resolved", "that", "metabolism" ]
[ { "code": "8A6Z", "title": "Epilepsy or seizures, unspecified" }, { "code": "8A60.5", "title": "Epilepsy due to injuries to the head" }, { "code": "8A61.1Z", "title": "Genetic epileptic syndromes with onset in infancy, unspecified" }, { "code": "8A06.Y/8A6Z", "title": "Myoclonus due to epilepsy" }, { "code": "8A61.40", "title": "Reflex epilepsies" }, { "code": "8E47", "title": "Encephalopathy, not elsewhere classified" }, { "code": "8D43.0Y&XM0ZH6", "title": "Encephalopathy due to lead" }, { "code": "NA07.0Y", "title": "Other specified concussion" }, { "code": "8D43.0Z", "title": "Encephalopathy due to toxicity, unspecified" }, { "code": "NE80.3", "title": "Other serum reactions" } ]
=== ICD-11 CODES FOUND === [8A6Z] Epilepsy or seizures, unspecified Also known as: Epilepsy or seizures, unspecified | Cerebral seizures | Seizure disorder | seizure disorder, so described | epilepsy NOS [8A60.5] Epilepsy due to injuries to the head Definition: Epilepsy occurring in relation to a traumatic brain injury. Onset is more than 1 week following the trauma, with risk increasing with the severity of brain injury. Also known as: Epilepsy due to injuries to the head | Post traumatic epilepsy | Traumatic epilepsy | traumatic epileptic [8A61.1Z] Genetic epileptic syndromes with onset in infancy, unspecified Also known as: Genetic epileptic syndromes with onset in infancy, unspecified | Genetic epileptic syndromes with onset in infancy | infantile epilepsy NOS [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 [8E47] Encephalopathy, not elsewhere classified Definition: Global brain dysfunction Also known as: Encephalopathy, not elsewhere classified | encephalopathy NEC | encephalopathy NOS | encephalopathy disease | encephalopathy syndrome [NA07.0Y] Other specified concussion Also known as: Other specified concussion | Dupré syndrome | Irritation of meninges | Traumatic encephalopathy [8D43.0Z] Encephalopathy due to toxicity, unspecified Also known as: Encephalopathy due to toxicity, unspecified | Encephalopathy due to toxicity | toxic encephalopathy | toxic brain fever | toxic brain inflammation [NE80.3] Other serum reactions Also known as: Other serum reactions | Allergic reaction to serum | serum allergy | Complications of vaccination, protein sickness | Protein sickness Excludes: serum hepatitis === GRAPH WALKS === --- Walk 1 --- [8A6Z] Epilepsy or seizures, unspecified --PARENT--> [?] Epilepsy or seizures Def: At least 2 unprovoked (or reflex) seizures occurring more than 24 hours apart.... --RELATED_TO--> [?] Sudden unexpected death in epilepsy Def: Sudden unexpected death in epilepsy (SUDEP) is a category of death in people with epilepsy that occurs under benign circumstances and in the absence of known structural causes of death (i.e. not due t... --- Walk 2 --- [8A6Z] Epilepsy or seizures, unspecified --PARENT--> [?] Epilepsy or seizures Def: At least 2 unprovoked (or reflex) seizures occurring more than 24 hours apart.... --RELATED_TO--> [?] Sudden unexpected death in epilepsy Def: Sudden unexpected death in epilepsy (SUDEP) is a category of death in people with epilepsy that occurs under benign circumstances and in the absence of known structural causes of death (i.e. not due t... --- Walk 3 --- [8A60.5] Epilepsy due to injuries to the head Def: Epilepsy occurring in relation to a traumatic brain injury. Onset is more than 1 week following the trauma, with risk increasing with the severity of brain injury.... --PARENT--> [8A60] Epilepsy due to structural or metabolic conditions or diseases Def: Epilepsy occurring in relation to a distinct other structural or metabolic condition or disease that has been demonstrated to be associated with a substantially increased risk of developing epilepsy.... --CHILD--> [8A60.2] Epilepsy due to degenerative brain disorders Def: Epilepsy in relation to a degenerative brain disorder known to be associated with seizures, such as certain neuronal storage disorders (e.g. adult neuronal ceroid lipofuscinosis), and certain mitochon... --- Walk 4 --- [8A60.5] Epilepsy due to injuries to the head Def: Epilepsy occurring in relation to a traumatic brain injury. Onset is more than 1 week following the trauma, with risk increasing with the severity of brain injury.... --PARENT--> [8A60] Epilepsy due to structural or metabolic conditions or diseases Def: Epilepsy occurring in relation to a distinct other structural or metabolic condition or disease that has been demonstrated to be associated with a substantially increased risk of developing epilepsy.... --CHILD--> [8A60.1] Epilepsy due to cerebrovascular disorders Def: Epilepsy occurring in relation to a stroke, with onset at least one week following an ischemic or haemorrhagic stroke.... --- Walk 5 --- [8A61.1Z] Genetic epileptic syndromes with onset in infancy, unspecified --PARENT--> [8A61.1] Genetic epileptic syndromes with onset in infancy Def: Include a vast spectrum of phenotypes having in common a genetic background and the onset in infancy. They range from benign self-remitting to severe drug resistant syndromes. Family history of epilep... --CHILD--> [8A61.12] Epilepsy of infancy with migrating focal seizures Def: Epilepsy syndrome with onset between the first week of life and seven months of intractable, polymorphous focal seizures. Psychomotor development progressively deteriorates. A mutation of SCN1A may be... --- Walk 6 --- [8A61.1Z] Genetic epileptic syndromes with onset in infancy, unspecified --PARENT--> [8A61.1] Genetic epileptic syndromes with onset in infancy Def: Include a vast spectrum of phenotypes having in common a genetic background and the onset in infancy. They range from benign self-remitting to severe drug resistant syndromes. Family history of epilep... --PARENT--> [8A61] Genetic or presumed genetic syndromes primarily expressed as epilepsy Def: The epilepsy is, as best as understood, the direct result of one or more known or presumed genetic defects in which seizures are the core symptom of the disorder....
[ "[8A6Z] Epilepsy or seizures, unspecified\n --PARENT--> [?] Epilepsy or seizures\n Def: At least 2 unprovoked (or reflex) seizures occurring more than 24 hours apart....\n --RELATED_TO--> [?] Sudden unexpected death in epilepsy\n Def: Sudden unexpected death in epilepsy (SUDEP) is a category of death in people with epilepsy that occurs under benign circumstances and in the absence of known structural causes of death (i.e. not due t...", "[8A6Z] Epilepsy or seizures, unspecified\n --PARENT--> [?] Epilepsy or seizures\n Def: At least 2 unprovoked (or reflex) seizures occurring more than 24 hours apart....\n --RELATED_TO--> [?] Sudden unexpected death in epilepsy\n Def: Sudden unexpected death in epilepsy (SUDEP) is a category of death in people with epilepsy that occurs under benign circumstances and in the absence of known structural causes of death (i.e. not due t...", "[8A60.5] Epilepsy due to injuries to the head\n Def: Epilepsy occurring in relation to a traumatic brain injury. Onset is more than 1 week following the trauma, with risk increasing with the severity of brain injury....\n --PARENT--> [8A60] Epilepsy due to structural or metabolic conditions or diseases\n Def: Epilepsy occurring in relation to a distinct other structural or metabolic condition or disease that has been demonstrated to be associated with a substantially increased risk of developing epilepsy....\n --CHILD--> [8A60.2] Epilepsy due to degenerative brain disorders\n Def: Epilepsy in relation to a degenerative brain disorder known to be associated with seizures, such as certain neuronal storage disorders (e.g. adult neuronal ceroid lipofuscinosis), and certain mitochon...", "[8A60.5] Epilepsy due to injuries to the head\n Def: Epilepsy occurring in relation to a traumatic brain injury. Onset is more than 1 week following the trauma, with risk increasing with the severity of brain injury....\n --PARENT--> [8A60] Epilepsy due to structural or metabolic conditions or diseases\n Def: Epilepsy occurring in relation to a distinct other structural or metabolic condition or disease that has been demonstrated to be associated with a substantially increased risk of developing epilepsy....\n --CHILD--> [8A60.1] Epilepsy due to cerebrovascular disorders\n Def: Epilepsy occurring in relation to a stroke, with onset at least one week following an ischemic or haemorrhagic stroke....", "[8A61.1Z] Genetic epileptic syndromes with onset in infancy, unspecified\n --PARENT--> [8A61.1] Genetic epileptic syndromes with onset in infancy\n Def: Include a vast spectrum of phenotypes having in common a genetic background and the onset in infancy. They range from benign self-remitting to severe drug resistant syndromes. Family history of epilep...\n --CHILD--> [8A61.12] Epilepsy of infancy with migrating focal seizures\n Def: Epilepsy syndrome with onset between the first week of life and seven months of intractable, polymorphous focal seizures. Psychomotor development progressively deteriorates. A mutation of SCN1A may be...", "[8A61.1Z] Genetic epileptic syndromes with onset in infancy, unspecified\n --PARENT--> [8A61.1] Genetic epileptic syndromes with onset in infancy\n Def: Include a vast spectrum of phenotypes having in common a genetic background and the onset in infancy. They range from benign self-remitting to severe drug resistant syndromes. Family history of epilep...\n --PARENT--> [8A61] Genetic or presumed genetic syndromes primarily expressed as epilepsy\n Def: The epilepsy is, as best as understood, the direct result of one or more known or presumed genetic defects in which seizures are the core symptom of the disorder...." ]
8A6Z
Epilepsy or seizures, unspecified
[ { "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" }, { "from_icd11": "8A6Z", "icd10_code": "G40919", "icd10_title": "Epilepsy, unspecified, intractable, without status epilepticus" }, { "from_icd11": "8A6Z", "icd10_code": "G40911", "icd10_title": "Epilepsy, unspecified, intractable, with status epilepticus" }, { "from_icd11": "8A6Z", "icd10_code": "G40419", "icd10_title": "Other generalized epilepsy and epileptic syndromes, intractable, without status epilepticus" }, { "from_icd11": "8A6Z", "icd10_code": "G40109", "icd10_title": "Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with simple partial seizures, not intractable, without status epilepticus" } ]
G40A09
Absence epileptic syndrome, not intractable, without status epilepticus
This patient is a 54-year-old homeless man with a history of schizophrenia who presented to the emergency department in November 2020 after being found down with a penetrating injury to the left anterior chest. On arrival, his GCS was 3, and he was being ventilated via bag valve mask by EMS. He was promptly intubated for airway protection. His vital signs were stable. On further exposure, he had an approximately 3 cm stab wound to his left anterior chest, medial to the nipple line, at approximately the level of the 7 th rib. Otherwise, he was noted to have ecchymosis of the occiput and superficial lacerations to his right flank. Also concerning was a fixed and dilated left pupil. A pan CT scan revealed a left subdural hematoma with bilateral frontal hemorrhagic contusions and 5 mm of midline shift. Additionally, he was found to have a moderate left-sided pneumothorax and associated left anterior 7 th rib fracture for which he underwent chest tube placement with resolution of his pneumothorax . A cerebral oxygenation monitor and drainage device was placed by neurosurgery revealing an elevated opening pressure of 31 mmHg. At this time, there was also concern for possible diaphragmatic injury given the location of his stab wound and imaging findings; however, in the setting of his elevated intracranial pressures, he was deemed unsafe for the OR and admitted to the neuro ICU for further monitoring.
3.685547
0.985352
sec[2]/p[0]
en
0.999997
34395014
https://doi.org/10.1155/2021/5531557
[ "chest", "this", "injury", "approximately", "stab", "wound", "pneumothorax", "homeless", "schizophrenia", "emergency" ]
[ { "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": "4A01.03", "title": "Transient hypogammaglobulinaemia of infancy" }, { "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" } ]
=== 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 [4A01.03] Transient hypogammaglobulinaemia of infancy Also known as: Transient hypogammaglobulinaemia of infancy | immunoglobulin maturational delay | THI - [transient hypogammaglobulinaemia of infancy] [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 === GRAPH WALKS === --- Walk 1 --- [CB7Z] Diseases of the respiratory system, unspecified --PARENT--> [12] Diseases of the respiratory system --CHILD--> [?] Upper respiratory tract disorders Def: This group of disorders refers to diseases of the upper airways (upper respiratory tract). The upper airways anatomically are complicated structures which extend from the airway openings at the nares ... --- Walk 2 --- [CB7Z] Diseases of the respiratory system, unspecified --PARENT--> [12] Diseases of the respiratory system --CHILD--> [?] Upper respiratory tract disorders Def: This group of disorders refers to diseases of the upper airways (upper respiratory tract). The upper airways anatomically are complicated structures which extend from the airway openings at the nares ... --- Walk 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... --EXCLUDES--> [?] Pleural effusion Def: Presence of fluid in the pleural cavity resulting from excessive transudation or exudation from the pleural surfaces.... --- Walk 4 --- [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... --EXCLUDES--> [?] Pleural effusion Def: Presence of fluid in the pleural cavity resulting from excessive transudation or exudation from the pleural surfaces.... --- Walk 5 --- [CA44] Pyothorax Def: Suppurative inflammation of the pleural space, typically due to acute bacterial infection. It can occur as a complication of pneumonia, thoracotomy, abscesses (lung, hepatic, or subdiaphragmatic), or ... --PARENT--> [?] Lung infections Def: Any condition of the lungs, caused by an infection with a bacterial, viral, fungal, or parasitic source.... --CHILD--> [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 ... --- Walk 6 --- [CA44] Pyothorax Def: Suppurative inflammation of the pleural space, typically due to acute bacterial infection. It can occur as a complication of pneumonia, thoracotomy, abscesses (lung, hepatic, or subdiaphragmatic), or ... --PARENT--> [?] Lung infections Def: Any condition of the lungs, caused by an infection with a bacterial, viral, fungal, or parasitic source.... --RELATED_TO--> [?] Chronic obstructive pulmonary disease with acute lower respiratory infection Def: Chronic obstructive pulmonary disease (COPD) with a lower respiratory tract infection usually caused by a virus or bacteria....
[ "[CB7Z] Diseases of the respiratory system, unspecified\n --PARENT--> [12] Diseases of the respiratory system\n --CHILD--> [?] Upper respiratory tract disorders\n Def: This group of disorders refers to diseases of the upper airways (upper respiratory tract). The upper airways anatomically are complicated structures which extend from the airway openings at the nares ...", "[CB7Z] Diseases of the respiratory system, unspecified\n --PARENT--> [12] Diseases of the respiratory system\n --CHILD--> [?] 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 ...", "[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 --EXCLUDES--> [?] Pleural effusion\n Def: Presence of fluid in the pleural cavity resulting from excessive transudation or exudation from the pleural surfaces....", "[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 --EXCLUDES--> [?] Pleural effusion\n Def: Presence of fluid in the pleural cavity resulting from excessive transudation or exudation from the pleural surfaces....", "[CA44] Pyothorax\n Def: Suppurative inflammation of the pleural space, typically due to acute bacterial infection. It can occur as a complication of pneumonia, thoracotomy, abscesses (lung, hepatic, or subdiaphragmatic), or ...\n --PARENT--> [?] Lung infections\n Def: Any condition of the lungs, caused by an infection with a bacterial, viral, fungal, or parasitic source....\n --CHILD--> [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 ...", "[CA44] Pyothorax\n Def: Suppurative inflammation of the pleural space, typically due to acute bacterial infection. It can occur as a complication of pneumonia, thoracotomy, abscesses (lung, hepatic, or subdiaphragmatic), or ...\n --PARENT--> [?] Lung infections\n Def: Any condition of the lungs, caused by an infection with a bacterial, viral, fungal, or parasitic source....\n --RELATED_TO--> [?] Chronic obstructive pulmonary disease with acute lower respiratory infection\n Def: Chronic obstructive pulmonary disease (COPD) with a lower respiratory tract infection usually caused by a virus or bacteria...." ]
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
Unfortunately, the horseshoe-shaped object had sharp and jagged edges. Our primary concern was a vocal cord injury during retrieval. As such, we entertained several different extraction modalities, including flexible bronchoscopy, rigid bronchoscopy, and, as a last resort, cardiothoracic surgery. After extensive discussion, an initial attempt with a flexible bronchoscope was agreed upon. After intubation with an 8.0 endotracheal tube, a flexible bronchoscope was introduced into the airway. Initially, under direct visualization, toothed forceps were used to dislodge the dental device from the bronchial wall. The resultant minor bleeding was controlled by instilling chilled saline. After mobilization, the forceps were also used to "aim" the dental device so that the rounded shape would cross the vocal cords first. Unfortunately, the forceps were unable to provide enough grip to ensure safe retrieval. To ensure a tighter grip, a lasso was introduced and threaded over and around the dental device. Using the lasso, the dental device was pulled up to the bronchoscope. Then, simultaneously, the dental device, bronchoscope, and endotracheal tube were all removed. Initially, likely because of the size of the dental device, the patient did experience bronchospasm complicated by hypoxia, requiring reintubation. Fortunately, after steroid treatment, the patient was safely extubated and able to return home.
3.794922
0.974609
sec[1]/p[3]
en
0.999996
37323356
https://doi.org/10.7759/cureus.39074
[ "dental", "device", "bronchoscope", "flexible", "forceps", "unfortunately", "vocal", "retrieval", "bronchoscopy", "endotracheal" ]
[ { "code": "DA07.3", "title": "Disturbances in tooth formation" }, { "code": "DA09.61", "title": "Periapical abscess with sinus" }, { "code": "QA00.8", "title": "Dental examination" }, { "code": "DA08.0", "title": "Dental caries" }, { "code": "DA08.4", "title": "Deposits on teeth" }, { "code": "8A43.Z", "title": "Neuromyelitis optica, unspecified" }, { "code": "QB5Z", "title": "Presence of unspecified device" }, { "code": "PL12.0", "title": "Structural device failure, as mode of injury or harm" }, { "code": "PL12.2", "title": "Perforation or protrusion by device, as mode of injury or harm" }, { "code": "PL12.1", "title": "Functional device failure, as mode of injury or harm" } ]
=== ICD-11 CODES FOUND === [DA07.3] Disturbances in tooth formation Definition: A group of conditions characterised by disturbances in tooth formation. Also known as: Disturbances in tooth formation | disturbance of tooth formation | Dental dysplasia | disorder of tooth formation | Florid cemento-osseous dysplasia Includes: Dental dysplasia | Florid cemento-osseous dysplasia | Regional odontodysplasia Excludes: Hutchinson teeth and mulberry molars in congenital syphilis | mottled teeth [DA09.61] Periapical abscess with sinus Also known as: Periapical abscess with sinus | Dental abscess with sinus | Dentoalveolar abscess with sinus | Dental sinus | periapical abscess fistula Includes: Dental abscess with sinus | Dentoalveolar abscess with sinus | Dental sinus [QA00.8] Dental examination Also known as: Dental examination | examination of teeth [DA08.0] Dental caries Definition: A condition characterised by localised destruction of calcified tissue, initiated on the tooth surface by decalcification of the enamel, followed by the enzymatic lysis of organic structures, resulting in cavity formation. Also known as: Dental caries | Dental decay | carious teeth | dental cavity | saprodontia Includes: Dental decay [DA08.4] Deposits on teeth Definition: In dentistry, calculus or tartar is a form of hardened dental plaque. Also known as: Deposits on teeth | Accretions on teeth | Extrinsic staining of teeth NOS | staining of teeth NOS | Betel deposits on teeth [8A43.Z] Neuromyelitis optica, unspecified Also known as: Neuromyelitis optica, unspecified | Neuromyelitis optica | Devic | Devic disease | Devic syndrome [QB5Z] Presence of unspecified device Also known as: Presence of unspecified device [PL12.0] Structural device failure, as mode of injury or harm Definition: Harm arising due to mechanical or material device failure not related to the installation of the device. Also known as: Structural device failure, as mode of injury or harm | part failure of a structural device as a mode of injury | structural device component failure as a mode of injury | structural device design failure as a mode of injury | manufacturing fault of a structural device as a mode of injury Includes: Leakage from device, as mode of injury or harm | Wear, breakage or breakdown of device, as mode of injury or harm | Breakdown of intraocular lens Excludes: Wear of articular bearing surface of joint prosthesis | Combination or interaction of operator error and device failure, as mode of injury or harm | Structural device failure without injury or harm [PL12.2] Perforation or protrusion by device, as mode of injury or harm Also known as: Perforation or protrusion by device, as mode of injury or harm | protruding device | pierced by device | Ocular Implant Extrusion | Ocular Implant Exposure Includes: Ocular Implant Extrusion | Ocular Implant Exposure Excludes: Cut, puncture or tear, as mode of injury or harm [PL12.1] Functional device failure, as mode of injury or harm Also known as: Functional device failure, as mode of injury or harm | faulty device | jamming of device | device failure to activate | Battery failure before end of battery life Excludes: Pacemaker or implantable cardioverter defibrillator dysfunction | Pacemaker or implantable cardioverter defibrillator battery at end of battery life | Combination or interaction of operator error and device failure, as mode of injury or harm === GRAPH WALKS === --- Walk 1 --- [DA07.3] Disturbances in tooth formation Def: A group of conditions characterised by disturbances in tooth formation.... --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.... --RELATED_TO--> [?] Oligodontia Def: A genetic condition characterised by the development of fewer than the normal number of teeth. The diagnosis of Oligodontia is usually made in cases in which more than six teeth are missing.... --- Walk 2 --- [DA07.3] Disturbances in tooth formation Def: A group of conditions characterised by disturbances in tooth formation.... --EXCLUDES--> [?] Mottling of enamel Def: Mottling occurs only when the dentition is permanently exposed to excessive fluoride during the development calcification of teeth.... --PARENT--> [?] Fluoride related opacities or lesions Def: This is a fluoride related abnormality in the tissue of an organism (in layman's terms, "damage"), usually caused by disease or trauma.... --- Walk 3 --- [DA09.61] Periapical abscess with sinus --PARENT--> [DA09.6] Periapical abscess --CHILD--> [DA09.61] Periapical abscess with sinus --- Walk 4 --- [DA09.61] Periapical abscess with sinus --PARENT--> [DA09.6] Periapical abscess --CHILD--> [DA09.61] Periapical abscess with sinus --- Walk 5 --- [QA00.8] Dental examination --PARENT--> [QA00] General examination or investigation of persons without complaint or reported diagnosis --EXCLUDES--> [?] Special screening examination for infectious diseases Def: A reason for encounter to screen for an infection with a bacterial, viral, fungal, or parasitic source.... --- Walk 6 --- [QA00.8] Dental examination --PARENT--> [QA00] General examination or investigation of persons without complaint or reported diagnosis --EXCLUDES--> [?] Special screening examination for infectious diseases Def: A reason for encounter to screen for an infection with a bacterial, viral, fungal, or parasitic source....
[ "[DA07.3] Disturbances in tooth formation\n Def: A group of conditions characterised by disturbances in tooth formation....\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 --RELATED_TO--> [?] Oligodontia\n Def: A genetic condition characterised by the development of fewer than the normal number of teeth. The diagnosis of Oligodontia is usually made in cases in which more than six teeth are missing....", "[DA07.3] Disturbances in tooth formation\n Def: A group of conditions characterised by disturbances in tooth formation....\n --EXCLUDES--> [?] Mottling of enamel\n Def: Mottling occurs only when the dentition is permanently exposed to excessive fluoride during the development calcification of teeth....\n --PARENT--> [?] Fluoride related opacities or lesions\n Def: This is a fluoride related abnormality in the tissue of an organism (in layman's terms, \"damage\"), usually caused by disease or trauma....", "[DA09.61] Periapical abscess with sinus\n --PARENT--> [DA09.6] Periapical abscess\n --CHILD--> [DA09.61] Periapical abscess with sinus", "[DA09.61] Periapical abscess with sinus\n --PARENT--> [DA09.6] Periapical abscess\n --CHILD--> [DA09.61] Periapical abscess with sinus", "[QA00.8] Dental examination\n --PARENT--> [QA00] General examination or investigation of persons without complaint or reported diagnosis\n --EXCLUDES--> [?] Special screening examination for infectious diseases\n Def: A reason for encounter to screen for an infection with a bacterial, viral, fungal, or parasitic source....", "[QA00.8] Dental examination\n --PARENT--> [QA00] General examination or investigation of persons without complaint or reported diagnosis\n --EXCLUDES--> [?] Special screening examination for infectious diseases\n Def: A reason for encounter to screen for an infection with a bacterial, viral, fungal, or parasitic source...." ]
DA07.3
Disturbances in tooth formation
[ { "from_icd11": "DA07.3", "icd10_code": "K004", "icd10_title": "Disturbances in tooth formation" }, { "from_icd11": "DA09.61", "icd10_code": "K046", "icd10_title": "Periapical abscess with sinus" }, { "from_icd11": "QA00.8", "icd10_code": "Z012", "icd10_title": "Encounter for dental examination and cleaning" }, { "from_icd11": "DA08.0", "icd10_code": "K027", "icd10_title": "Dental root caries" }, { "from_icd11": "DA08.0", "icd10_code": "K0263", "icd10_title": "Dental caries on smooth surface penetrating into pulp" }, { "from_icd11": "DA08.0", "icd10_code": "K0253", "icd10_title": "Dental caries on pit and fissure surface penetrating into pulp" }, { "from_icd11": "DA08.0", "icd10_code": "K029", "icd10_title": "Dental caries, unspecified" }, { "from_icd11": "DA08.0", "icd10_code": "K02", "icd10_title": "Dental caries" }, { "from_icd11": "DA08.0", "icd10_code": "K020", "icd10_title": "" }, { "from_icd11": "DA08.0", "icd10_code": "K021", "icd10_title": "" }, { "from_icd11": "DA08.0", "icd10_code": "K022", "icd10_title": "" }, { "from_icd11": "DA08.0", "icd10_code": "K023", "icd10_title": "Arrested dental caries" }, { "from_icd11": "DA08.0", "icd10_code": "K024", "icd10_title": "" }, { "from_icd11": "DA08.0", "icd10_code": "K025", "icd10_title": "Dental caries on pit and fissure surface" }, { "from_icd11": "DA08.0", "icd10_code": "K028", "icd10_title": "" } ]
K004
Disturbances in tooth formation
In September of 2022, she began seeing a pain management specialist at the Florida Spine Institute for chronic pain due to fibromyalgia and rheumatoid arthritis that had been worsening despite her treatment regimen at that time. During this visit, the doctor first suggested ketamine treatment for her pain as well as her depression. In October, she began taking 30 mg ketamine capsules daily, which was then increased to three times daily in December. On December 19, 2022, she began a 10-day IV ketamine infusion per protocol as a treatment for her depression. She reported that this was her first time ever trying ketamine treatment and immediately saw hopeful results. These infusions were administered according to the pain management doctor's prescribed protocol, using a starting dose of 150 mg of ketamine alongside 10 mg of lidocaine, 4 mg of ondansetron, and 25 mg of promethazine to prevent nausea and vomiting. She successfully completed this treatment with no adverse effects and reported improved mood and energy by the end of the first round of infusion. By her third treatment, she reported great improvement in her depression, resulting in increased socialization and activity compared to her usual state. In January of 2023, she continued using ketamine hydrochloride (HCL) powder and was prescribed 30 mg ketamine lozenges three times daily. She continued follow-up infusions for two days per week.
3.611328
0.974609
sec[1]/p[1]
en
0.999997
PMC11342591
https://doi.org/10.7759/cureus.65261
[ "ketamine", "pain", "that", "this", "depression", "daily", "time", "doctor", "three", "times" ]
[ { "code": "NE60", "title": "Harmful effects of drugs, medicaments or biological substances, not elsewhere classified" }, { "code": "PB21&XM7C11", "title": "Unintentional exposure to or harmful effects of ketamine" }, { "code": "PC91&XM7C11", "title": "Intentional self-harm by exposure to or harmful effects of ketamine" }, { "code": "6C4D.2Z", "title": "Dissociative drug dependence including ketamine or PCP, unspecified" }, { "code": "6C4D.3", "title": "Dissociative drug intoxication including Ketamine or PCP" }, { "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 === [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 [6C4D.2Z] Dissociative drug dependence including ketamine or PCP, unspecified Also known as: Dissociative drug dependence including ketamine or PCP, unspecified | Dissociative drug dependence including ketamine or PCP | Dissociative drug addiction including ketamine or PCP [6C4D.3] Dissociative drug intoxication including Ketamine or PCP Definition: Dissociative drug intoxication including Ketamine and PCP is a clinically significant transient condition that develops during or shortly after the consumption of a dissociative drug that is characterised by disturbances in consciousness, cognition, perception, affect, behaviour, or coordination. These disturbances are caused by the known pharmacological effects of a dissociative drug and their intensity is closely related to the amount of the dissociative drug consumed. They are time-limited an Also known as: Dissociative drug intoxication including Ketamine or PCP | PCP intoxication | phencyclidine intoxication [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 --- [NE60] Harmful effects of drugs, medicaments or biological substances, not elsewhere classified --EXCLUDES--> [?] Alcohol intoxication Def: Alcohol intoxication is a clinically significant transient condition that develops during or shortly after the consumption of alcohol that is characterised by disturbances in consciousness, cognition,... --PARENT--> [?] 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 2 --- [NE60] Harmful effects of drugs, medicaments or biological substances, not elsewhere classified --EXCLUDES--> [?] Alcohol intoxication Def: Alcohol intoxication is a clinically significant transient condition that develops during or shortly after the consumption of alcohol that is characterised by disturbances in consciousness, cognition,... --EXCLUDES--> [?] Harmful effects of or exposure to noxious substances chiefly nonmedicinal as to source, alcohols --- Walk 3 --- [6C4D.2Z] Dissociative drug dependence including ketamine or PCP, unspecified --PARENT--> [6C4D.2] Dissociative drug dependence including ketamine or PCP Def: Dissociative drug dependence including ketamine or PCP is a disorder of regulation of dissociative drug use arising from repeated or continuous use of dissociative drugs. The characteristic feature is... --CHILD--> [6C4D.20] Dissociative drug dependence including Ketamine or PCP, current use Def: Dissociative drug dependence including Ketamine and PCP, current use refers to use of dissociative drugs within the past month.... --- Walk 4 --- [6C4D.2Z] Dissociative drug dependence including ketamine or PCP, unspecified --PARENT--> [6C4D.2] Dissociative drug dependence including ketamine or PCP Def: Dissociative drug dependence including ketamine or PCP is a disorder of regulation of dissociative drug use arising from repeated or continuous use of dissociative drugs. The characteristic feature is... --CHILD--> [6C4D.21] Dissociative drug dependence including ketamine or PCP, early full remission Def: After a diagnosis of Dissociative drug dependence including ketamine and PCP, and often following a treatment episode or other intervention (including self-help intervention), the individual has been ... --- Walk 5 --- [6C4D.3] Dissociative drug intoxication including Ketamine or PCP Def: Dissociative drug intoxication including Ketamine and PCP is a clinically significant transient condition that develops during or shortly after the consumption of a dissociative drug that is character... --PARENT--> [6C4D] Disorders due to use of dissociative drugs including ketamine and phencyclidine [PCP] Def: Disorders due to use of dissociative drugs including ketamine and phencyclidine [PCP] are characterised by the pattern and consequences of dissociative drug use. Dissociative drugs include ketamine an... --CHILD--> [6C4D.2] Dissociative drug dependence including ketamine or PCP Def: Dissociative drug dependence including ketamine or PCP is a disorder of regulation of dissociative drug use arising from repeated or continuous use of dissociative drugs. The characteristic feature is... --- Walk 6 --- [6C4D.3] Dissociative drug intoxication including Ketamine or PCP Def: Dissociative drug intoxication including Ketamine and PCP is a clinically significant transient condition that develops during or shortly after the consumption of a dissociative drug that is character... --PARENT--> [6C4D] Disorders due to use of dissociative drugs including ketamine and phencyclidine [PCP] Def: Disorders due to use of dissociative drugs including ketamine and phencyclidine [PCP] are characterised by the pattern and consequences of dissociative drug use. Dissociative drugs include ketamine an... --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...
[ "[NE60] Harmful effects of drugs, medicaments or biological substances, not elsewhere classified\n --EXCLUDES--> [?] Alcohol intoxication\n Def: Alcohol intoxication is a clinically significant transient condition that develops during or shortly after the consumption of alcohol that is characterised by disturbances in consciousness, cognition,...\n --PARENT--> [?] 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...", "[NE60] Harmful effects of drugs, medicaments or biological substances, not elsewhere classified\n --EXCLUDES--> [?] Alcohol intoxication\n Def: Alcohol intoxication is a clinically significant transient condition that develops during or shortly after the consumption of alcohol that is characterised by disturbances in consciousness, cognition,...\n --EXCLUDES--> [?] Harmful effects of or exposure to noxious substances chiefly nonmedicinal as to source, alcohols", "[6C4D.2Z] Dissociative drug dependence including ketamine or PCP, unspecified\n --PARENT--> [6C4D.2] Dissociative drug dependence including ketamine or PCP\n Def: Dissociative drug dependence including ketamine or PCP is a disorder of regulation of dissociative drug use arising from repeated or continuous use of dissociative drugs. The characteristic feature is...\n --CHILD--> [6C4D.20] Dissociative drug dependence including Ketamine or PCP, current use\n Def: Dissociative drug dependence including Ketamine and PCP, current use refers to use of dissociative drugs within the past month....", "[6C4D.2Z] Dissociative drug dependence including ketamine or PCP, unspecified\n --PARENT--> [6C4D.2] Dissociative drug dependence including ketamine or PCP\n Def: Dissociative drug dependence including ketamine or PCP is a disorder of regulation of dissociative drug use arising from repeated or continuous use of dissociative drugs. The characteristic feature is...\n --CHILD--> [6C4D.21] Dissociative drug dependence including ketamine or PCP, early full remission\n Def: After a diagnosis of Dissociative drug dependence including ketamine and PCP, and often following a treatment episode or other intervention (including self-help intervention), the individual has been ...", "[6C4D.3] Dissociative drug intoxication including Ketamine or PCP\n Def: Dissociative drug intoxication including Ketamine and PCP is a clinically significant transient condition that develops during or shortly after the consumption of a dissociative drug that is character...\n --PARENT--> [6C4D] Disorders due to use of dissociative drugs including ketamine and phencyclidine [PCP]\n Def: Disorders due to use of dissociative drugs including ketamine and phencyclidine [PCP] are characterised by the pattern and consequences of dissociative drug use. Dissociative drugs include ketamine an...\n --CHILD--> [6C4D.2] Dissociative drug dependence including ketamine or PCP\n Def: Dissociative drug dependence including ketamine or PCP is a disorder of regulation of dissociative drug use arising from repeated or continuous use of dissociative drugs. The characteristic feature is...", "[6C4D.3] Dissociative drug intoxication including Ketamine or PCP\n Def: Dissociative drug intoxication including Ketamine and PCP is a clinically significant transient condition that develops during or shortly after the consumption of a dissociative drug that is character...\n --PARENT--> [6C4D] Disorders due to use of dissociative drugs including ketamine and phencyclidine [PCP]\n Def: Disorders due to use of dissociative drugs including ketamine and phencyclidine [PCP] are characterised by the pattern and consequences of dissociative drug use. Dissociative drugs include ketamine an...\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..." ]
NE60
Harmful effects of drugs, medicaments or biological substances, not elsewhere classified
[ { "from_icd11": "NE60", "icd10_code": "T50A95A", "icd10_title": "Adverse effect of other bacterial vaccines, initial encounter" }, { "from_icd11": "NE60", "icd10_code": "T50Z15A", "icd10_title": "Adverse effect of immunoglobulin, initial encounter" }, { "from_icd11": "NE60", "icd10_code": "T50Z95A", "icd10_title": "Adverse effect of other vaccines and biological substances, initial encounter" }, { "from_icd11": "NE60", "icd10_code": "T50A95S", "icd10_title": "Adverse effect of other bacterial vaccines, sequela" }, { "from_icd11": "NE60", "icd10_code": "T50B95A", "icd10_title": "Adverse effect of other viral vaccines, initial encounter" }, { "from_icd11": "NE60", "icd10_code": "T50A25A", "icd10_title": "Adverse effect of mixed bacterial vaccines without a pertussis component, initial encounter" }, { "from_icd11": "NE60", "icd10_code": "T50A91A", "icd10_title": "Poisoning by other bacterial vaccines, accidental (unintentional), initial encounter" }, { "from_icd11": "NE60", "icd10_code": "T498X5A", "icd10_title": "Adverse effect of other topical agents, initial encounter" }, { "from_icd11": "NE60", "icd10_code": "T48905A", "icd10_title": "Adverse effect of unspecified agents primarily acting on the respiratory system, initial encounter" }, { "from_icd11": "NE60", "icd10_code": "T48995A", "icd10_title": "Adverse effect of other agents primarily acting on the respiratory system, initial encounter" }, { "from_icd11": "NE60", "icd10_code": "T50A15A", "icd10_title": "Adverse effect of pertussis vaccine, including combinations with a pertussis component, initial encounter" }, { "from_icd11": "NE60", "icd10_code": "T50B15A", "icd10_title": "Adverse effect of smallpox vaccines, initial encounter" }, { "from_icd11": "NE60", "icd10_code": "T416X3A", "icd10_title": "" }, { "from_icd11": "NE60", "icd10_code": "T419X3A", "icd10_title": "" }, { "from_icd11": "NE60", "icd10_code": "T418X2A", "icd10_title": "" } ]
T50A95A
Adverse effect of other bacterial vaccines, initial encounter
We present a patient with autosomal recessive osteopetrosis 8. The clinical features of the proband are typical of the ARO phenotype such as increased bone density, large skull, bone-in-bone, thrombocytopenia, hepatosplenomegaly, loss of vision and “sandwich vertebrae”. We identified a deletion-insertion variant, NC_000007.14:g.26263639_26335651delinsCA in the homozygous state on chromosome 7 by genome sequencing. Exome sequencing failed to identify the large deletion because it encompasses a large noncoding region including the intergenic region upstream of SNX10 , there showing that exome sequencing is not an ideal method for identifying large deletions in noncoding regions. Genome sequencing identified the exact breakpoints of the 72,012 bp long region encompassing the regulatory region of SNX10 . The parents are healthy carriers of the same variant. Initially, we thought that due to the deletion of the 5′-UTR and exon 1 region of SNX10, there might be no SNX10 transcript, but a study by Ye et al., 2015 showed severe osteopetrosis but no rickets in the osteoclast-specific SNX10 knockout. However, our patient showed a moderate phenotype without rickets. Further mRNA analysis revealed the presence of a lower amount of SNX10 transcript. Therefore, we hypothesize that the decreased amount of SNX10 transcript results in abnormal endosome sorting and vesicular transport to osteoclast bone lacunae.
4.226563
0.488525
sec[3]/p[0]
en
0.999998
36526684
https://doi.org/10.1038/s10038-022-01104-2
[ "region", "bone", "large", "sequencing", "deletion", "that", "transcript", "osteopetrosis", "phenotype", "variant" ]
[ { "code": "ND56.0", "title": "Superficial injury of unspecified body region" }, { "code": "ND56.Z", "title": "Unspecified injury to unspecified part of trunk, limb or body region" }, { "code": "CA44", "title": "Pyothorax" }, { "code": "FB3Z", "title": "Disorders of muscles, unspecified" }, { "code": "ND56.8", "title": "Traumatic amputation of unspecified body region" }, { "code": "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 === [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 [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 --- [ND56.0] Superficial injury of unspecified body region --EXCLUDES--> [?] Superficial injuries involving multiple body regions --CHILD--> [?] Superficial injuries involving head with neck --- Walk 2 --- [ND56.0] Superficial injury of unspecified body region --RELATED_TO--> [?] Haematoma of surgical wound of skin Def: Collection of blood within skin and soft tissues following surgical wound of skin usually resulting from defective haemostasis... --PARENT--> [?] Haemorrhage or haematoma complicating a procedure, not elsewhere classified --- Walk 3 --- [ND56.Z] Unspecified injury to unspecified part of trunk, limb or body region --PARENT--> [ND56] Injury of unspecified body region Def: Damage inflicted on the body in an unspecified area as the direct or indirect result of an external force, with or without disruption of structural continuity.... --CHILD--> [ND56.1] Open wound of unspecified body region --- Walk 4 --- [ND56.Z] Unspecified injury to unspecified part of trunk, limb or body region --PARENT--> [ND56] Injury of unspecified body region Def: Damage inflicted on the body in an unspecified area as the direct or indirect result of an external force, with or without disruption of structural continuity.... --CHILD--> [ND56.1] Open wound of unspecified body region --- Walk 5 --- [CA44] Pyothorax Def: Suppurative inflammation of the pleural space, typically due to acute bacterial infection. It can occur as a complication of pneumonia, thoracotomy, abscesses (lung, hepatic, or subdiaphragmatic), or ... --EXCLUDES--> [?] Tuberculous pleurisy, without mention of bacteriological or histological confirmation Def: This is a common, and in many cases lethal, infectious disease caused by various strains of mycobacteria, usually Mycobacterium tuberculosis, with an inflammation of the pleura. This diagnosis is with... --EXCLUDES--> [?] Primary respiratory tuberculosis without mention of bacteriological or histological confirmation Def: This is a common, and in many cases lethal, infectious disease of the respiratory caused by various strains of mycobacteria, usually Mycobacterium tuberculosis. This diagnosis is without mention of ba... --- Walk 6 --- [CA44] Pyothorax Def: Suppurative inflammation of the pleural space, typically due to acute bacterial infection. It can occur as a complication of pneumonia, thoracotomy, abscesses (lung, hepatic, or subdiaphragmatic), or ... --EXCLUDES--> [?] Tuberculous pleurisy, without mention of bacteriological or histological confirmation Def: This is a common, and in many cases lethal, infectious disease caused by various strains of mycobacteria, usually Mycobacterium tuberculosis, with an inflammation of the pleura. This diagnosis is with... --CHILD--> [?] Bronchopleural tuberculosis
[ "[ND56.0] Superficial injury of unspecified body region\n --EXCLUDES--> [?] Superficial injuries involving multiple body regions\n --CHILD--> [?] Superficial injuries involving head with neck", "[ND56.0] Superficial injury of unspecified body region\n --RELATED_TO--> [?] Haematoma of surgical wound of skin\n Def: Collection of blood within skin and soft tissues following surgical wound of skin usually resulting from defective haemostasis...\n --PARENT--> [?] Haemorrhage or haematoma complicating a procedure, not elsewhere classified", "[ND56.Z] Unspecified injury to unspecified part of trunk, limb or body region\n --PARENT--> [ND56] Injury of unspecified body region\n Def: Damage inflicted on the body in an unspecified area as the direct or indirect result of an external force, with or without disruption of structural continuity....\n --CHILD--> [ND56.1] Open wound of unspecified body region", "[ND56.Z] Unspecified injury to unspecified part of trunk, limb or body region\n --PARENT--> [ND56] Injury of unspecified body region\n Def: Damage inflicted on the body in an unspecified area as the direct or indirect result of an external force, with or without disruption of structural continuity....\n --CHILD--> [ND56.1] Open wound of unspecified body region", "[CA44] Pyothorax\n Def: Suppurative inflammation of the pleural space, typically due to acute bacterial infection. It can occur as a complication of pneumonia, thoracotomy, abscesses (lung, hepatic, or subdiaphragmatic), or ...\n --EXCLUDES--> [?] Tuberculous pleurisy, without mention of bacteriological or histological confirmation\n Def: This is a common, and in many cases lethal, infectious disease caused by various strains of mycobacteria, usually Mycobacterium tuberculosis, with an inflammation of the pleura. This diagnosis is with...\n --EXCLUDES--> [?] Primary respiratory tuberculosis without mention of bacteriological or histological confirmation\n Def: This is a common, and in many cases lethal, infectious disease of the respiratory caused by various strains of mycobacteria, usually Mycobacterium tuberculosis. This diagnosis is without mention of ba...", "[CA44] Pyothorax\n Def: Suppurative inflammation of the pleural space, typically due to acute bacterial infection. It can occur as a complication of pneumonia, thoracotomy, abscesses (lung, hepatic, or subdiaphragmatic), or ...\n --EXCLUDES--> [?] Tuberculous pleurisy, without mention of bacteriological or histological confirmation\n Def: This is a common, and in many cases lethal, infectious disease caused by various strains of mycobacteria, usually Mycobacterium tuberculosis, with an inflammation of the pleura. This diagnosis is with...\n --CHILD--> [?] Bronchopleural tuberculosis" ]
ND56.0
Superficial injury of unspecified body region
[ { "from_icd11": "ND56.0", "icd10_code": "T009", "icd10_title": "" }, { "from_icd11": "ND56.0", "icd10_code": "T140", "icd10_title": "" }, { "from_icd11": "ND56.Z", "icd10_code": "T1491XA", "icd10_title": "Suicide attempt, initial encounter" }, { "from_icd11": "ND56.Z", "icd10_code": "T1490XS", "icd10_title": "Injury, unspecified, sequela" }, { "from_icd11": "ND56.Z", "icd10_code": "T1490", "icd10_title": "Injury, unspecified" }, { "from_icd11": "ND56.Z", "icd10_code": "T1491", "icd10_title": "Suicide attempt" }, { "from_icd11": "ND56.Z", "icd10_code": "T1490XA", "icd10_title": "Injury, unspecified, initial encounter" }, { "from_icd11": "ND56.Z", "icd10_code": "T148XXS", "icd10_title": "Other injury of unspecified body region, sequela" }, { "from_icd11": "ND56.Z", "icd10_code": "T148XXD", "icd10_title": "Other injury of unspecified body region, subsequent encounter" }, { "from_icd11": "ND56.Z", "icd10_code": "T148", "icd10_title": "Other injury of unspecified body region" }, { "from_icd11": "ND56.Z", "icd10_code": "T14", "icd10_title": "Injury of unspecified body region" }, { "from_icd11": "ND56.Z", "icd10_code": "T149", "icd10_title": "Unspecified injury" }, { "from_icd11": "CA44", "icd10_code": "J869", "icd10_title": "Pyothorax without fistula" }, { "from_icd11": "CA44", "icd10_code": "J860", "icd10_title": "Pyothorax with fistula" }, { "from_icd11": "CA44", "icd10_code": "J85-J86", "icd10_title": "" } ]
T009
In March 2021, the patient complained of dizziness and headache, accompanied by nausea and vomiting, without numbness or disturbance of movement in the limbs. The patient did not pay attention to these and had not undergone further examination until June 2021. The patient was treated in Yunnan Cancer Hospital for liver cirrhosis; MRI examination found a space-occupying lesion in the left frontotemporal lobe, but further specific diagnosis and treatment were still not performed. Then, the patient developed blurred vision and double vision and went to the First Affiliated Hospital of Kunming Medical University for treatment. Head MRI examination revealed a shallow lobulated round mass (approximately 4.4×4.6×4.9 cm) with slightly long T2 and T1 signals under the left frontal cranial plate. FLAIR showed a slightly high signal, and the boundary was still clear. DWI showed high signal enhancement and obvious enhancement, and the adjacent dura mater was slightly thickened and enhanced. Moreover, the adjacent brain parenchyma was obviously compressed, and a large area of oedema and a right-skewed midline structure were observed. MRA showed that the compression of the bilateral anterior cerebral artery was shifted to the right, the A1 segment of the left anterior cerebral artery was slender, the distal part was well developed, and the M1 segment of the left middle cerebral artery was shifted downwards .
3.857422
0.983887
sec[1]/p[1]
en
0.999996
PMC10370419
https://doi.org/10.3389/fonc.2023.1209244
[ "slightly", "cerebral", "artery", "still", "vision", "signal", "enhancement", "adjacent", "shifted", "segment" ]
[ { "code": "1D00.Z", "title": "Infectious encephalitis, unspecified" }, { "code": "8E7Y", "title": "Other specified diseases of the nervous system" }, { "code": "8B20", "title": "Stroke not known if ischaemic or haemorrhagic" }, { "code": "8B1Z", "title": "Cerebral ischaemia, unspecified" }, { "code": "8B11.5Z", "title": "Cerebral ischaemic stroke, unspecified" }, { "code": "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" } ]
=== ICD-11 CODES FOUND === [1D00.Z] Infectious encephalitis, unspecified Also known as: Infectious encephalitis, unspecified | Infectious encephalitis, not elsewhere classified | encephalitis NOS | acute encephalitis NOS | acute brain inflammation [8E7Y] Other specified diseases of the nervous system Also known as: Other specified diseases of the nervous system | Circumscribed brain atrophy | circumscribed cerebral atrophy | atrophic lobar sclerosis | atrophic lobar brain sclerosis [8B20] Stroke not known if ischaemic or haemorrhagic Definition: Fulfills criteria for stroke in acute symptoms of focal brain injury that have lasted 24 hours or more (or led to death before 24 hours), but subtype of stroke (ischemic or haemorrhagic) has not been determined by neuroimaging or other techniques. Also known as: Stroke not known if ischaemic or haemorrhagic | apoplexy | brain vascular accident | cerebral accident | cerebral apoplexy Excludes: sequelae of stroke [8B1Z] Cerebral ischaemia, unspecified Also known as: Cerebral ischaemia, unspecified | brain ischaemia | cerebrovascular ischaemic disease | cerebrovascular ischaemia | cerebral anaemia [8B11.5Z] Cerebral ischaemic stroke, unspecified Also known as: Cerebral ischaemic stroke, unspecified | Cerebral ischaemic stroke of unknown cause | cryptogenic stroke | occlusion and stenosis of cerebral and precerebral arteries, resulting in cerebral infarction | cerebral infarct [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 === GRAPH WALKS === --- Walk 1 --- [1D00.Z] Infectious encephalitis, unspecified --PARENT--> [1D00] Infectious encephalitis, not elsewhere classified Def: A disease of the brain, caused by an infection.... --CHILD--> [1D00.2] Parasitic or protozoal encephalitis Def: A disease of the brain, caused by an infection with a parasitic or protozoal source.... --- Walk 2 --- [1D00.Z] Infectious encephalitis, unspecified --PARENT--> [1D00] Infectious encephalitis, not elsewhere classified Def: A disease of the brain, caused by an infection.... --CHILD--> [1D00.0] Bacterial encephalitis --- Walk 3 --- [8E7Y] Other specified diseases of the nervous system --PARENT--> [08] Diseases of the nervous system Def: This is a group of conditions characterised as being in or associated with the nervous system.... --RELATED_TO--> [?] Structural developmental anomalies of the nervous system Def: Any condition caused by failure of the nervous system to correctly develop during the antenatal period.... --- Walk 4 --- [8E7Y] Other specified diseases of the nervous system --PARENT--> [08] Diseases of the nervous system Def: This is a group of conditions characterised as being in or associated with the nervous system.... --EXCLUDES--> [?] Certain conditions originating in the perinatal period Def: This chapter includes conditions that have their origin in the perinatal period even though death or morbidity occurs later.... --- Walk 5 --- [8B20] Stroke not known if ischaemic or haemorrhagic Def: Fulfills criteria for stroke in acute symptoms of focal brain injury that have lasted 24 hours or more (or led to death before 24 hours), but subtype of stroke (ischemic or haemorrhagic) has not been ... --EXCLUDES--> [?] Late effects of stroke not known if ischaemic or haemorrhagic Def: Late effects occurring 1 month or later after the onset of the disease. Codes for acute stroke should be exclusively used for the acute stroke and immediately related hospitalisation episodes.... --PARENT--> [?] Late effects of cerebrovascular disease Def: Effects of cerebrovascular disease 1 month or later after the onset of the disease. Codes for acute stroke should be exclusively used for the acute stroke and immediately related hospitalisation episo... --- Walk 6 --- [8B20] Stroke not known if ischaemic or haemorrhagic Def: Fulfills criteria for stroke in acute symptoms of focal brain injury that have lasted 24 hours or more (or led to death before 24 hours), but subtype of stroke (ischemic or haemorrhagic) has not been ... --PARENT--> [?] 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... --CHILD--> [?] Cerebral ischaemia
[ "[1D00.Z] Infectious encephalitis, unspecified\n --PARENT--> [1D00] Infectious encephalitis, not elsewhere classified\n Def: A disease of the brain, caused by an infection....\n --CHILD--> [1D00.2] Parasitic or protozoal encephalitis\n Def: A disease of the brain, caused by an infection with a parasitic or protozoal source....", "[1D00.Z] Infectious encephalitis, unspecified\n --PARENT--> [1D00] Infectious encephalitis, not elsewhere classified\n Def: A disease of the brain, caused by an infection....\n --CHILD--> [1D00.0] Bacterial encephalitis", "[8E7Y] Other specified diseases of the nervous system\n --PARENT--> [08] Diseases of the nervous system\n Def: This is a group of conditions characterised as being in or associated with the nervous system....\n --RELATED_TO--> [?] Structural developmental anomalies of the nervous system\n Def: Any condition caused by failure of the nervous system to correctly develop during the antenatal period....", "[8E7Y] Other specified diseases of the nervous system\n --PARENT--> [08] Diseases of the nervous system\n Def: This is a group of conditions characterised as being in or associated with the nervous system....\n --EXCLUDES--> [?] Certain conditions originating in the perinatal period\n Def: This chapter includes conditions that have their origin in the perinatal period even though death or morbidity occurs later....", "[8B20] Stroke not known if ischaemic or haemorrhagic\n Def: Fulfills criteria for stroke in acute symptoms of focal brain injury that have lasted 24 hours or more (or led to death before 24 hours), but subtype of stroke (ischemic or haemorrhagic) has not been ...\n --EXCLUDES--> [?] Late effects of stroke not known if ischaemic or haemorrhagic\n Def: Late effects occurring 1 month or later after the onset of the disease. Codes for acute stroke should be exclusively used for the acute stroke and immediately related hospitalisation episodes....\n --PARENT--> [?] Late effects of cerebrovascular disease\n Def: Effects of cerebrovascular disease 1 month or later after the onset of the disease. Codes for acute stroke should be exclusively used for the acute stroke and immediately related hospitalisation episo...", "[8B20] Stroke not known if ischaemic or haemorrhagic\n Def: Fulfills criteria for stroke in acute symptoms of focal brain injury that have lasted 24 hours or more (or led to death before 24 hours), but subtype of stroke (ischemic or haemorrhagic) has not been ...\n --PARENT--> [?] 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...\n --CHILD--> [?] Cerebral ischaemia" ]
1D00.Z
Infectious encephalitis, unspecified
[ { "from_icd11": "1D00.Z", "icd10_code": "G0490", "icd10_title": "Encephalitis and encephalomyelitis, unspecified" }, { "from_icd11": "1D00.Z", "icd10_code": "G0491", "icd10_title": "Myelitis, unspecified" }, { "from_icd11": "1D00.Z", "icd10_code": "G0430", "icd10_title": "Acute necrotizing hemorrhagic encephalopathy, unspecified" }, { "from_icd11": "1D00.Z", "icd10_code": "G0431", "icd10_title": "Postinfectious acute necrotizing hemorrhagic encephalopathy" }, { "from_icd11": "1D00.Z", "icd10_code": "G0439", "icd10_title": "Other acute necrotizing hemorrhagic encephalopathy" }, { "from_icd11": "1D00.Z", "icd10_code": "G0481", "icd10_title": "Other encephalitis and encephalomyelitis" }, { "from_icd11": "1D00.Z", "icd10_code": "G0489", "icd10_title": "Other myelitis" }, { "from_icd11": "1D00.Z", "icd10_code": "G04", "icd10_title": "Encephalitis, myelitis and encephalomyelitis" }, { "from_icd11": "1D00.Z", "icd10_code": "G048", "icd10_title": "Other encephalitis, myelitis and encephalomyelitis" }, { "from_icd11": "8B20", "icd10_code": "I64", "icd10_title": "" }, { "from_icd11": "8B1Z", "icd10_code": "I67848", "icd10_title": "Other cerebrovascular vasospasm and vasoconstriction" }, { "from_icd11": "8B1Z", "icd10_code": "I6789", "icd10_title": "Other cerebrovascular disease" }, { "from_icd11": "8B1Z", "icd10_code": "I6782", "icd10_title": "Cerebral ischemia" }, { "from_icd11": "8B1Z", "icd10_code": "I6781", "icd10_title": "Acute cerebrovascular insufficiency" }, { "from_icd11": "8B1Z", "icd10_code": "I67841", "icd10_title": "Reversible cerebrovascular vasoconstriction syndrome" } ]
G0490
Encephalitis and encephalomyelitis, unspecified
After treatment, the patient's oxygenation improved, the peak airway pressure decreased, and the pulmonary static compliance increased (Table 1 ). Leukocytes, high procalcitonin, C-reactive protein, and interleukin-6decreased to normal. On day 10, the patient stopped prone ventilation, adjusted the depth of sedation to shallow sedation (CPOT 0, RASS –2 to 0), and adjusted the ventilator mode to synchronized intermittent mandatory ventilation (SIMV PC 10cmH 2 0, PS 10cmH 2 0, PEEP 8cmH 2 0, F12 breaths min –1 , FiO 2 40%). The changes of ECMO and ventilator parameters are shown in Table 1 . ECMO support was stopped on day 12, tracheal intubation was removed after 2 days, and sequential transnasal high flow oxygen inhalation was applied. The patient was transferred to the respiratory department on day 15 and discharged after 12 days. During the treatment, we intermittently used bedside chest X-ray and CT scans of chest to understand the pulmonary lesions. Bedside chest X-ray showed that the right lung lesions are less severe than before on day 5 and 8 . After the patient's condition was slightly stable, we began to perform CT scans of chest intermittently, and the results showed that the lung lesions gradually improved . During the treatment, the patient's tolerance and compliance were good, and no adverse events occurred. Two months later, follow-up showed that the patient was in good condition.
3.810547
0.970215
sec[1]/p[4]
en
0.999997
PMC8735805
https://doi.org/10.1097/MD.0000000000028482
[ "chest", "lesions", "that", "improved", "pulmonary", "compliance", "ventilation", "adjusted", "sedation", "ventilator" ]
[ { "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--> [?] 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 --- [CB7Z] Diseases of the respiratory system, unspecified --PARENT--> [12] Diseases of the respiratory system --EXCLUDES--> [?] Endocrine, nutritional or metabolic diseases Def: This chapter includes endocrine diseases, nutritional diseases as well as metabolic diseases.... --- Walk 3 --- [CB27] Pleural effusion Def: Presence of fluid in the pleural cavity resulting from excessive transudation or exudation from the pleural surfaces.... --EXCLUDES--> [?] 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... --PARENT--> [?] Symptoms or signs involving the respiratory system --- Walk 4 --- [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... --PARENT--> [?] Symptoms or signs involving the respiratory system --- Walk 5 --- [CA44] Pyothorax Def: Suppurative inflammation of the pleural space, typically due to acute bacterial infection. It can occur as a complication of pneumonia, thoracotomy, abscesses (lung, hepatic, or subdiaphragmatic), or ... --EXCLUDES--> [?] Tuberculous pleurisy, without mention of bacteriological or histological confirmation Def: This is a common, and in many cases lethal, infectious disease caused by various strains of mycobacteria, usually Mycobacterium tuberculosis, with an inflammation of the pleura. This diagnosis is with... --CHILD--> [?] Tuberculous empyema, without mention of bacteriological or histological confirmation --- Walk 6 --- [CA44] Pyothorax Def: Suppurative inflammation of the pleural space, typically due to acute bacterial infection. It can occur as a complication of pneumonia, thoracotomy, abscesses (lung, hepatic, or subdiaphragmatic), or ... --PARENT--> [?] Lung infections Def: Any condition of the lungs, caused by an infection with a bacterial, viral, fungal, or parasitic source.... --RELATED_TO--> [?] Chronic obstructive pulmonary disease with acute lower respiratory infection Def: Chronic obstructive pulmonary disease (COPD) with a lower respiratory tract infection usually caused by a virus or bacteria....
[ "[CB7Z] Diseases of the respiratory system, unspecified\n --PARENT--> [12] Diseases of the respiratory 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....", "[CB7Z] Diseases of the respiratory system, unspecified\n --PARENT--> [12] Diseases of the respiratory system\n --EXCLUDES--> [?] Endocrine, nutritional or metabolic diseases\n Def: This chapter includes endocrine diseases, nutritional diseases as well as metabolic diseases....", "[CB27] Pleural effusion\n Def: Presence of fluid in the pleural cavity resulting from excessive transudation or exudation from the pleural surfaces....\n --EXCLUDES--> [?] 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 --PARENT--> [?] Symptoms or signs involving the respiratory system", "[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 --PARENT--> [?] Symptoms or signs involving the respiratory system", "[CA44] Pyothorax\n Def: Suppurative inflammation of the pleural space, typically due to acute bacterial infection. It can occur as a complication of pneumonia, thoracotomy, abscesses (lung, hepatic, or subdiaphragmatic), or ...\n --EXCLUDES--> [?] Tuberculous pleurisy, without mention of bacteriological or histological confirmation\n Def: This is a common, and in many cases lethal, infectious disease caused by various strains of mycobacteria, usually Mycobacterium tuberculosis, with an inflammation of the pleura. This diagnosis is with...\n --CHILD--> [?] Tuberculous empyema, without mention of bacteriological or histological confirmation", "[CA44] Pyothorax\n Def: Suppurative inflammation of the pleural space, typically due to acute bacterial infection. It can occur as a complication of pneumonia, thoracotomy, abscesses (lung, hepatic, or subdiaphragmatic), or ...\n --PARENT--> [?] Lung infections\n Def: Any condition of the lungs, caused by an infection with a bacterial, viral, fungal, or parasitic source....\n --RELATED_TO--> [?] Chronic obstructive pulmonary disease with acute lower respiratory infection\n Def: Chronic obstructive pulmonary disease (COPD) with a lower respiratory tract infection usually caused by a virus or bacteria...." ]
CB7Z
Diseases of the respiratory system, unspecified
[ { "from_icd11": "CB7Z", "icd10_code": "J989", "icd10_title": "Respiratory disorder, unspecified" }, { "from_icd11": "CB7Z", "icd10_code": "X", "icd10_title": "" }, { "from_icd11": "CB7Z", "icd10_code": "J09-J18", "icd10_title": "" }, { "from_icd11": "CB27", "icd10_code": "J910", "icd10_title": "Malignant pleural effusion" }, { "from_icd11": "CB27", "icd10_code": "J918", "icd10_title": "Pleural effusion in other conditions classified elsewhere" }, { "from_icd11": "CB27", "icd10_code": "J90", "icd10_title": "Pleural effusion, not elsewhere classified" }, { "from_icd11": "CB27", "icd10_code": "J90-J94", "icd10_title": "" }, { "from_icd11": "CB27", "icd10_code": "J91", "icd10_title": "Pleural effusion in conditions classified elsewhere" }, { "from_icd11": "CA44", "icd10_code": "J869", "icd10_title": "Pyothorax without fistula" }, { "from_icd11": "CA44", "icd10_code": "J860", "icd10_title": "Pyothorax with fistula" }, { "from_icd11": "CA44", "icd10_code": "J85-J86", "icd10_title": "" }, { "from_icd11": "CA44", "icd10_code": "J86", "icd10_title": "Pyothorax" }, { "from_icd11": "MD30.Z", "icd10_code": "R0781", "icd10_title": "Pleurodynia" }, { "from_icd11": "MD30.Z", "icd10_code": "R0782", "icd10_title": "Intercostal pain" }, { "from_icd11": "MD30.Z", "icd10_code": "R079", "icd10_title": "Chest pain, unspecified" } ]
J989
Respiratory disorder, unspecified
A 45-year-old man with chest discomfort on effort was referred to our hospital. He had been treated for hypertension, hyperlipidemia, hyperuricemia, and diabetes mellitus for 5 years. He had a current smoking habit and a body mass index of 35 indicating obesity, and no family history. Coronary angiography demonstrated severe coronary artery disease including severe stenosis of the left anterior descending artery, the diagonal branch, and the right coronary artery, as well as total occlusion of the left circumflex artery . Further examinations also revealed severe stenosis of the left internal carotid artery without any neurological symptoms . Because this was a marginal case for carotid artery revascularization, discussion was held to discern between the neurosurgery and cardiac surgery departments, with neurosurgeons suggesting that preemptive carotid artery stenting was not necessary. They recommended that blood pressure and hemoglobin levels be maintained during CABG, and that antiplatelet therapy be started as soon as possible following the procedure. Fig. 1 a Preoperative left coronary angiography showing severe stenosis of the left circumflex and left anterior descending arteries. b Preoperative right coronary angiography showing severe stenosis of the right coronary artery. c Preoperative computed tomography scan showing severe stenosis of the left common carotid artery (white arrowhead)
3.775391
0.982422
sec[1]/p[0]
en
0.999996
36650524
https://doi.org/10.1186/s13019-023-02135-2
[ "artery", "coronary", "stenosis", "carotid", "angiography", "that", "preoperative", "descending", "circumflex", "chest" ]
[ { "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": "BA8Z", "title": "Diseases of coronary artery, unspecified" }, { "code": "BA4Z", "title": "Acute ischaemic heart disease, unspecified" }, { "code": "BA41.Z", "title": "Acute myocardial infarction, unspecified" }, { "code": "BA5Z", "title": "Chronic ischaemic heart disease, unspecified" }, { "code": "LA8C.2", "title": "Congenital coronary arterial fistula" } ]
=== ICD-11 CODES FOUND === [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 [BA8Z] Diseases of coronary artery, unspecified Also known as: Diseases of coronary artery, unspecified | coronary artery insufficiency | coronary artery heart disease | CAD - [coronary artery disease] | coronary artery disorder [BA4Z] Acute ischaemic heart disease, unspecified Also known as: Acute ischaemic heart disease, unspecified | acute coronary syndrome | ACS - [acute coronary syndrome] | Silent myocardial ischaemia | asymptomatic ischemia [BA41.Z] Acute myocardial infarction, unspecified Also known as: Acute myocardial infarction, unspecified | Acute myocardial infarction | cardiac attack | heart attack | acute cardiac infarction [BA5Z] Chronic ischaemic heart disease, unspecified Also known as: Chronic ischaemic heart disease, unspecified | Ischaemic heart disease (chronic) NOS | coronary ischaemia | coronary damage NOS | atheroma of heart [LA8C.2] Congenital coronary arterial fistula Definition: A congenital cardiovascular malformation in which a coronary artery communicates, through an anomalous channel, with a cardiac chamber or with any segment of the systemic or pulmonary circulation. Additional information: this communication may be simple and direct or may be tortuous and dilated. In order of frequency the involved coronary artery is the right, the left and, rarely, both coronary arteries. Occasionally multiple fistulas are present. Also known as: Congenital coronary arterial fistula | coronary fistula | congenital arteriovenous coronary fistula | congenital coronary fistula to pulmonary artery | Congenital coronary arterial fistula to right ventricle Includes: congenital coronary fistula to pulmonary artery Excludes: anomalous origin of coronary artery from pulmonary arterial tree === GRAPH WALKS === --- Walk 1 --- [BD5Z] Diseases of arteries or arterioles, unspecified --PARENT--> [?] Diseases of arteries or arterioles --CHILD--> [?] Chronic arterial occlusive disease --- 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 --- [BD52] Certain specified disorders of arteries or arterioles --EXCLUDES--> [?] Acute arterial occlusion --CHILD--> [?] Acute aortoiliac occlusion --- Walk 4 --- [BD52] Certain specified disorders of arteries or arterioles --EXCLUDES--> [?] Nonorgan specific systemic autoimmune disorders --CHILD--> [?] Lupus erythematosus Def: An autoimmune non-organ specific inflammatory disease characterised by the presence of antibodies to DNA, RNA and other components of the nucleus. It has a very variable clinical presentation and cour... --- Walk 5 --- [BD52.3] Rupture of artery --EXCLUDES--> [?] Injury, poisoning or certain other consequences of external causes Def: !markdown In the ICD, injury means physical or physiological bodily harm resulting from interaction of the body with energy (mechanical, thermal, electrical, chemical or radiant, or due to extreme pre... --EXCLUDES--> [?] Certain specified obstetric trauma Def: Any injury characterised by maternal trauma. These injuries are caused by or subsequent to the process of (or any intervention related to) pregnancy, or labour and delivery.... --- Walk 6 --- [BD52.3] Rupture of artery --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... --CHILD--> [?] Injuries to the thorax
[ "[BD5Z] Diseases of arteries or arterioles, unspecified\n --PARENT--> [?] Diseases of arteries or arterioles\n --CHILD--> [?] Chronic arterial occlusive disease", "[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--> [?] Acute arterial occlusion\n --CHILD--> [?] Acute aortoiliac occlusion", "[BD52] Certain specified disorders of arteries or arterioles\n --EXCLUDES--> [?] Nonorgan specific systemic autoimmune disorders\n --CHILD--> [?] Lupus erythematosus\n Def: An autoimmune non-organ specific inflammatory disease characterised by the presence of antibodies to DNA, RNA and other components of the nucleus. It has a very variable clinical presentation and cour...", "[BD52.3] Rupture of artery\n --EXCLUDES--> [?] Injury, poisoning or certain other consequences of external causes\n Def: !markdown\nIn the ICD, injury means physical or physiological bodily harm resulting from interaction of the body with energy (mechanical, thermal, electrical, chemical or radiant, or due to extreme pre...\n --EXCLUDES--> [?] Certain specified obstetric trauma\n Def: Any injury characterised by maternal trauma. These injuries are caused by or subsequent to the process of (or any intervention related to) pregnancy, or labour and delivery....", "[BD52.3] Rupture of artery\n --EXCLUDES--> [?] Injury, poisoning or certain other consequences of external causes\n Def: !markdown\nIn the ICD, injury means physical or physiological bodily harm resulting from interaction of the body with energy (mechanical, thermal, electrical, chemical or radiant, or due to extreme pre...\n --CHILD--> [?] Injuries to the thorax" ]
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 49-year-old male patient presented with a venous leg ulcer at his right lower leg . Relevant comorbidities included DM, HT, hyperlipidaemia, and a medical history of thrombosis of the right lower leg without acute signs of ischemia. Previous treatments with antiseptic dressing with silver nanoparticles for seven weeks were ineffective. Upon presentation, the wound dimensions were 5 cm in length, 3 cm in width, and 1.5 cm in depth. The wound consisted of 90% of granulation tissue, 5% slough, and 5% epithelialization tissue. Low levels of exudate (thin, water-like) were produced. Local signs of infection included pain, malodour, and delayed healing. A wound swab confirmed the presence of Enterococcus faecalis (resistant to trimethoprim + sulphonamide, neomycin, clindamycin, gentamicin; and sensitive to ampicillin, nitrofurantoin, bacitracin, ciprofloxacin, chloramphenicol). Pain level was 5 during the daytime and 8 during treatment. L-Mesitran ® Soft (MGH) was applied to the wound and L-Mesitran ® Foam was applied as a secondary dressing. Dressing changes were performed by the patient at home at 48 h intervals. Pain and malodour levels gradually decreased and after 14 days of treatment, the pain was absent during the daytime (VAS score of 0) and at level 1 during treatment. Only L-Mesitran ® Foam was applied. The wound was completely healed after 17 days of MGH treatment without complications .
3.927734
0.981445
sec[1]/sec[8]/p[0]
en
0.999997
34438968
https://doi.org/10.3390/antibiotics10080918
[ "wound", "pain", "dressing", "mesitran", "included", "without", "tissue", "malodour", "daytime", "foam" ]
[ { "code": "MD11.5", "title": "Dyspnoea" }, { "code": "NB32.3Z", "title": "Injury of lung, unspecified" }, { "code": "NB91.1Z", "title": "Injury of liver, unspecified" }, { "code": "NA01.Z&XA9T94", "title": "Temporal wound" }, { "code": "ND56.1", "title": "Open wound of unspecified body region" }, { "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 === [MD11.5] Dyspnoea Definition: Dyspnoea is used to describe perceptions of difficulty or distress related to breathing and is recognised as symptomatic of disease when it occurs under inappropriate circumstances. Dyspnoea is a presenting complaint of patients with a wide variety of medical diseases by multiple mechanisms. Dyspnoea is considered acute when it lasts from hours up to 3 weeks, subacute from 3 weeks up to 8 weeks, and chronic dyspnoea lasts more than 8 weeks. Also known as: Dyspnoea | difficulty breathing | respiration difficult | short of breath | winded Includes: Orthopnoea Excludes: Transient tachypnoea of newborn [NB32.3Z] Injury of lung, unspecified Also known as: Injury of lung, unspecified | Certain injuries of lung | injury of lung NOS | acute lung injury NOS | lung wound NOS [NB91.1Z] Injury of liver, unspecified Also known as: Injury of liver, unspecified | Injury of liver | liver wound NOS | liver fracture NOS | hepatocellular injury [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 [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 --- [MD11.5] Dyspnoea Def: Dyspnoea is used to describe perceptions of difficulty or distress related to breathing and is recognised as symptomatic of disease when it occurs under inappropriate circumstances. Dyspnoea is a pres... --PARENT--> [MD11] Abnormalities of breathing Def: Abnormalities of breathing includes dyspnoea, stridor, wheezing, periodic breathing, hyperventilation, mouth breathing, hiccough, sneezing, and other abnormalities of breathing.... --EXCLUDES--> [?] Respiratory arrest Def: Arrest of spontaneous breathing.... --- Walk 2 --- [MD11.5] Dyspnoea Def: Dyspnoea is used to describe perceptions of difficulty or distress related to breathing and is recognised as symptomatic of disease when it occurs under inappropriate circumstances. Dyspnoea is a pres... --EXCLUDES--> [?] Transient tachypnoea of newborn Def: Transient tachypnoea of newborn is usually a benign self-limiting illness of term and near-term infants demonstrating increased respiratory rate and requiring supplementary oxygen after birth.... --PARENT--> [?] Respiratory distress of newborn Def: A condition characterised by developmental insufficiency of surfactant associated proteins or surfactant production and structural immaturity in the lungs.... --- Walk 3 --- [NB32.3Z] Injury of lung, unspecified --PARENT--> [NB32.3] Certain injuries of lung --CHILD--> [NB32.31] Laceration of lung --- Walk 4 --- [NB32.3Z] Injury of lung, unspecified --PARENT--> [NB32.3] Certain injuries of lung --CHILD--> [NB32.31] Laceration of lung --- Walk 5 --- [NB91.1Z] Injury of liver, unspecified --PARENT--> [NB91.1] Injury of liver Def: Damage inflicted on the liver as the direct or indirect result of an external force, with or without disruption of structural continuity.... --RELATED_TO--> [?] Birth injury to liver Def: Rupture or subcapsular haemorrhage into the liver parenchyma as a result of birth trauma usually seen in large for gestational age infants, those with hepatomegaly, those born by breech delivery; may ... --- Walk 6 --- [NB91.1Z] Injury of liver, unspecified --PARENT--> [NB91.1] Injury of liver Def: Damage inflicted on the liver as the direct or indirect result of an external force, with or without disruption of structural continuity.... --RELATED_TO--> [?] Birth injury to liver Def: Rupture or subcapsular haemorrhage into the liver parenchyma as a result of birth trauma usually seen in large for gestational age infants, those with hepatomegaly, those born by breech delivery; may ...
[ "[MD11.5] Dyspnoea\n Def: Dyspnoea is used to describe perceptions of difficulty or distress related to breathing and is recognised as symptomatic of disease when it occurs under inappropriate circumstances. Dyspnoea is a pres...\n --PARENT--> [MD11] Abnormalities of breathing\n Def: Abnormalities of breathing includes dyspnoea, stridor, wheezing, periodic breathing, hyperventilation, mouth breathing, hiccough, sneezing, and other abnormalities of breathing....\n --EXCLUDES--> [?] Respiratory arrest\n Def: Arrest of spontaneous breathing....", "[MD11.5] Dyspnoea\n Def: Dyspnoea is used to describe perceptions of difficulty or distress related to breathing and is recognised as symptomatic of disease when it occurs under inappropriate circumstances. Dyspnoea is a pres...\n --EXCLUDES--> [?] Transient tachypnoea of newborn\n Def: Transient tachypnoea of newborn is usually a benign self-limiting illness of term and near-term infants demonstrating increased respiratory rate and requiring supplementary oxygen after birth....\n --PARENT--> [?] Respiratory distress of newborn\n Def: A condition characterised by developmental insufficiency of surfactant associated proteins or surfactant production and structural immaturity in the lungs....", "[NB32.3Z] Injury of lung, unspecified\n --PARENT--> [NB32.3] Certain injuries of lung\n --CHILD--> [NB32.31] Laceration of lung", "[NB32.3Z] Injury of lung, unspecified\n --PARENT--> [NB32.3] Certain injuries of lung\n --CHILD--> [NB32.31] Laceration of lung", "[NB91.1Z] Injury of liver, unspecified\n --PARENT--> [NB91.1] Injury of liver\n Def: Damage inflicted on the liver as the direct or indirect result of an external force, with or without disruption of structural continuity....\n --RELATED_TO--> [?] Birth injury to liver\n Def: Rupture or subcapsular haemorrhage into the liver parenchyma as a result of birth trauma usually seen in large for gestational age infants, those with hepatomegaly, those born by breech delivery; may ...", "[NB91.1Z] Injury of liver, unspecified\n --PARENT--> [NB91.1] Injury of liver\n Def: Damage inflicted on the liver as the direct or indirect result of an external force, with or without disruption of structural continuity....\n --RELATED_TO--> [?] Birth injury to liver\n Def: Rupture or subcapsular haemorrhage into the liver parenchyma as a result of birth trauma usually seen in large for gestational age infants, those with hepatomegaly, those born by breech delivery; may ..." ]
MD11.5
Dyspnoea
[ { "from_icd11": "MD11.5", "icd10_code": "R0603", "icd10_title": "Acute respiratory distress" }, { "from_icd11": "MD11.5", "icd10_code": "R0601", "icd10_title": "Orthopnea" }, { "from_icd11": "MD11.5", "icd10_code": "R0602", "icd10_title": "Shortness of breath" }, { "from_icd11": "MD11.5", "icd10_code": "R0600", "icd10_title": "Dyspnea, unspecified" }, { "from_icd11": "MD11.5", "icd10_code": "R0609", "icd10_title": "Other forms of dyspnea" }, { "from_icd11": "MD11.5", "icd10_code": "R060", "icd10_title": "Dyspnea" }, { "from_icd11": "NB32.3Z", "icd10_code": "S27321A", "icd10_title": "Contusion of lung, unilateral, initial encounter" }, { "from_icd11": "NB32.3Z", "icd10_code": "S27322A", "icd10_title": "Contusion of lung, bilateral, initial encounter" }, { "from_icd11": "NB32.3Z", "icd10_code": "S27331S", "icd10_title": "Laceration of lung, unilateral, sequela" }, { "from_icd11": "NB32.3Z", "icd10_code": "S27331A", "icd10_title": "Laceration of lung, unilateral, initial encounter" }, { "from_icd11": "NB32.3Z", "icd10_code": "S27329A", "icd10_title": "Contusion of lung, unspecified, initial encounter" }, { "from_icd11": "NB32.3Z", "icd10_code": "S27339A", "icd10_title": "Laceration of lung, unspecified, initial encounter" }, { "from_icd11": "NB32.3Z", "icd10_code": "S27391A", "icd10_title": "Other injuries of lung, unilateral, initial encounter" }, { "from_icd11": "NB32.3Z", "icd10_code": "S27391S", "icd10_title": "Other injuries of lung, unilateral, sequela" }, { "from_icd11": "NB32.3Z", "icd10_code": "S27321D", "icd10_title": "Contusion of lung, unilateral, subsequent encounter" } ]
R0603
Acute respiratory distress
Our patient, a 75-year-old male, had a left inguinoscrotal swelling for 12 years. He had no complaints as the hernia was reducible for 12 years. The patient had consistently declined to have surgery. He arrived at our emergency department complaining of terrible cramping, stomach discomfort, and distension, which had been going on for the previous five days. During this time, he did not have a bowel movement or passed any flatus. He restricted his intake to mere sips of water for the past five days. He had absolutely no urinary complaints. Physical examination revealed a moderately nourished man in severe distress from abdominal pain with a centrally distended abdomen. He was severely dehydrated and pale and gave the impression of being seriously ill. The patient’s blood pressure was 90/60 mmHg, pulse rate was 128/min, and temperature was 98.8 °F. Abdominal examination revealed a large, hard, and tender mass in the left inguinal region extending into the scrotum. The swelling measured 7 x 5 inches and was fixed and irreducible. There was guarding and rigidity as per abdominal examination. The left cord structures were palpable at the base of the penis, and the left testis was palpable vaguely at the tip of the swelling; right-sided cord structures and testis were normally palpable. No bowel sounds could be heard. The prostate gland was enlarged, and the rectum was vacant and free of any tumors.
3.587891
0.988281
sec[1]/p[0]
en
0.999997
37674969
https://doi.org/10.7759/cureus.43028
[ "swelling", "abdominal", "palpable", "complaints", "five", "bowel", "cord", "structures", "testis", "inguinoscrotal" ]
[ { "code": "FA36.Z", "title": "Effusion of joint, unspecified" }, { "code": "MA01.Z", "title": "Enlarged lymph nodes, unspecified" }, { "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": "GB90.Y", "title": "Other specified disorders of kidney or ureter" }, { "code": "MD81.3", "title": "Acute abdomen" }, { "code": "JA01.0", "title": "Abdominal pregnancy" }, { "code": "ME04.Z", "title": "Ascites, unspecified" }, { "code": "NB51.0&XA3KX0", "title": "Laceration without foreign body of abdominal wall" }, { "code": "NB9Y", "title": "Other specified injuries to the abdomen, lower back, lumbar spine or pelvis" } ]
=== ICD-11 CODES FOUND === [FA36.Z] Effusion of joint, unspecified Also known as: Effusion of joint, unspecified | Effusion of joint | effusion into joint | effusion of joint, site unspecified | hydrarthrosis [MA01.Z] Enlarged lymph nodes, unspecified Also known as: Enlarged lymph nodes, unspecified | Enlarged lymph nodes | swollen glands | Lymphadenopathy | adenopathy [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 [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 [MD81.3] Acute abdomen Definition: A clinical syndrome with acute abdominal pain that is severe, and rapid onset. Acute abdomen may be caused by a variety of disorders, injuries, or diseases Also known as: Acute abdomen | acute abdominal pain syndrome | surgical abdomen | abdominal acute syndrome | severe abdomen pain [JA01.0] Abdominal pregnancy Definition: A condition characterised by implantation of the embryo within the peritoneal cavity during pregnancy. Also known as: Abdominal pregnancy | abdomen pregnancy | intraperitoneal pregnancy Excludes: Maternal care for viable fetus in abdominal pregnancy | Delivery of viable fetus in abdominal pregnancy [ME04.Z] Ascites, unspecified Also known as: Ascites, unspecified | Ascites | abdominal dropsy | hydrops abdominis | ascites NOS [NB9Y] Other specified injuries to the abdomen, lower back, lumbar spine or pelvis Also known as: Other specified injuries to the abdomen, lower back, lumbar spine or pelvis | Abdominal wall trauma | Injury of pelvic floor | pelvic floor blunt injury | pelvic floor blunt trauma === GRAPH WALKS === --- Walk 1 --- [FA36.Z] Effusion of joint, unspecified --PARENT--> [FA36] Effusion of joint Def: Increased intra-articular fluid secondary to trauma and/or other acquired conditions not detailed in other codes.... --CHILD--> [FA36.Y] Other specified effusion of joint --- Walk 2 --- [FA36.Z] Effusion of joint, unspecified --PARENT--> [FA36] Effusion of joint Def: Increased intra-articular fluid secondary to trauma and/or other acquired conditions not detailed in other codes.... --EXCLUDES--> [?] Tertiary yaws Def: Tertiary yaws develops in <10% of untreated infected individuals after and interval of 5 years or more. The late stage skin lesions are characterised by gummatous nodules with necrotic tissue destruct... --- Walk 3 --- [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--> [MA01.0] Localised lymph node enlargement --- Walk 4 --- [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 --- Walk 5 --- [MD82] Intra-abdominal or pelvic swelling, mass or lump Def: 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.... --EXCLUDES--> [?] Ascites Def: Accumulation or retention of free fluid in the abdominal peritoneal cavity between the tissues lining the abdomen and abdominal organs. The fluid may be serous, haemorrhagic, or the result of inflamma... --CHILD--> [?] Fluid in peritoneal cavity --- Walk 6 --- [MD82] Intra-abdominal or pelvic swelling, mass or lump Def: 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.... --EXCLUDES--> [?] Ascites Def: Accumulation or retention of free fluid in the abdominal peritoneal cavity between the tissues lining the abdomen and abdominal organs. The fluid may be serous, haemorrhagic, or the result of inflamma... --CHILD--> [?] Fluid in peritoneal cavity
[ "[FA36.Z] Effusion of joint, unspecified\n --PARENT--> [FA36] Effusion of joint\n Def: Increased intra-articular fluid secondary to trauma and/or other acquired conditions not detailed in other codes....\n --CHILD--> [FA36.Y] Other specified effusion of joint", "[FA36.Z] Effusion of joint, unspecified\n --PARENT--> [FA36] Effusion of joint\n Def: Increased intra-articular fluid secondary to trauma and/or other acquired conditions not detailed in other codes....\n --EXCLUDES--> [?] Tertiary yaws\n Def: Tertiary yaws develops in <10% of untreated infected individuals after and interval of 5 years or more. The late stage skin lesions are characterised by gummatous nodules with necrotic tissue destruct...", "[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--> [MA01.0] Localised lymph node enlargement", "[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", "[MD82] Intra-abdominal or pelvic swelling, mass or lump\n Def: 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....\n --EXCLUDES--> [?] Ascites\n Def: Accumulation or retention of free fluid in the abdominal peritoneal cavity between the tissues lining the abdomen and abdominal organs. The fluid may be serous, haemorrhagic, or the result of inflamma...\n --CHILD--> [?] Fluid in peritoneal cavity", "[MD82] Intra-abdominal or pelvic swelling, mass or lump\n Def: 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....\n --EXCLUDES--> [?] Ascites\n Def: Accumulation or retention of free fluid in the abdominal peritoneal cavity between the tissues lining the abdomen and abdominal organs. The fluid may be serous, haemorrhagic, or the result of inflamma...\n --CHILD--> [?] Fluid in peritoneal cavity" ]
FA36.Z
Effusion of joint, unspecified
[ { "from_icd11": "FA36.Z", "icd10_code": "M25471", "icd10_title": "Effusion, right ankle" }, { "from_icd11": "FA36.Z", "icd10_code": "M25461", "icd10_title": "Effusion, right knee" }, { "from_icd11": "FA36.Z", "icd10_code": "M25462", "icd10_title": "Effusion, left knee" }, { "from_icd11": "FA36.Z", "icd10_code": "M25431", "icd10_title": "Effusion, right wrist" }, { "from_icd11": "FA36.Z", "icd10_code": "M25472", "icd10_title": "Effusion, left ankle" }, { "from_icd11": "FA36.Z", "icd10_code": "M25451", "icd10_title": "Effusion, right hip" }, { "from_icd11": "FA36.Z", "icd10_code": "M2548", "icd10_title": "Effusion, other site" }, { "from_icd11": "FA36.Z", "icd10_code": "M25411", "icd10_title": "Effusion, right shoulder" }, { "from_icd11": "FA36.Z", "icd10_code": "M25441", "icd10_title": "Effusion, right hand" }, { "from_icd11": "FA36.Z", "icd10_code": "M25452", "icd10_title": "Effusion, left hip" }, { "from_icd11": "FA36.Z", "icd10_code": "M25421", "icd10_title": "Effusion, right elbow" }, { "from_icd11": "FA36.Z", "icd10_code": "M25432", "icd10_title": "Effusion, left wrist" }, { "from_icd11": "FA36.Z", "icd10_code": "M25473", "icd10_title": "Effusion, unspecified ankle" }, { "from_icd11": "FA36.Z", "icd10_code": "M25412", "icd10_title": "Effusion, left shoulder" }, { "from_icd11": "FA36.Z", "icd10_code": "M25422", "icd10_title": "Effusion, left elbow" } ]
M25471
Effusion, right ankle
Severe Parkinsonism and AM after VPS was diagnosed. The therapy of Madopar (levodopa/benserazide) and Pramipexole was initiated. Over the next 2 weeks, the dose of Madopar and Pramipexole slowly increased to 550/137.5 mg/day and 1.125 mg/day, respectively. Nearly a month after initiation of treatment, the patient let out a long-lost weak cry leading to an emotional moment for the family. After that, he began to pronounce monosyllabic words and was able to stand and walk with assistance. A complete recovery of speech and motor skills was observed 2 months later. The patient could not recall the events he had experienced during the period of severe illness. At a 6-month follow-up post-treatment, head MRI scan showed no ventricular dilation. The regions of interest (ROI) of cortex (frontal lobe, parietal lobe, temporal lobe, occipital lobe and cingulate gyrus) and subcortex (putamen, caudate nucleus, thalamus and midbrain) were delineated on 18 F-FDG PET/MR images. The uptake value of each ROI was normalized by cerebellum to obtain the standard uptake value ratio of FDG (FDG-SUVR). Compared with before levodopa treatment, FDG-SUVR of all ROIs increased significantly after 6 months of treatment ( Table 1 ). Over the next year, the doses of Madopar and Pramipexole were gradually reduced until they were discontinued. The patient's neurological symptoms have not recurred during the 10-month follow-up.
4.007813
0.950684
sec[1]/p[3]
en
0.999997
PMC10272721
https://doi.org/10.3389/fneur.2023.1184713
[ "lobe", "madopar", "pramipexole", "levodopa", "over", "next", "uptake", "suvr", "parkinsonism", "diagnosed" ]
[ { "code": "CB40.2", "title": "Pulmonary collapse" }, { "code": "LA75.0", "title": "Accessory lobe of lung" }, { "code": "MD41", "title": "Clinical findings on diagnostic imaging of lung" }, { "code": "LA75.1", "title": "Agenesis of lung" }, { "code": "JA8A.1", "title": "Malformation of placenta" }, { "code": "MB22.5", "title": "Increased goal-directed activity" }, { "code": "DA0E.5Y", "title": "Other specified malocclusion" }, { "code": "5B80.0Z", "title": "Overweight, unspecified" }, { "code": "NE60", "title": "Harmful effects of drugs, medicaments or biological substances, not elsewhere classified" }, { "code": "MG43.1", "title": "Overeating" } ]
=== ICD-11 CODES FOUND === [CB40.2] Pulmonary collapse Also known as: Pulmonary collapse | Atelectasis | lung collapse | pulmonary atelectasis | pulmonary collapse with atelectasis Includes: Atelectasis Excludes: Primary atelectasis of newborn | tuberculous atelectasis, not confirmed | tuberculous atelectasis, confirmed [LA75.0] Accessory lobe of lung Definition: An extra lobe of lung beyond the 3 on the right and the 2 on the left Also known as: Accessory lobe of lung | supernumerary lung lobe | azygos lobe of lung | azygos lobe fissure of lung | azygos lobe [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 [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 [JA8A.1] Malformation of placenta Also known as: Malformation of placenta | variation of placenta form | deformity of placenta | placental deformity | Abnormal placenta NOS [MB22.5] Increased goal-directed activity Definition: Increased planning of and participation in multiple activities (e.g. sexual, occupational, political, religious), compared to the individual's typical level of activity. Also known as: Increased goal-directed activity | overactivity | behaviour of overactivity [DA0E.5Y] Other specified malocclusion Also known as: Other specified malocclusion | Crossbite | overbite | openbite | excessive overbite Includes: Crossbite [5B80.0Z] Overweight, unspecified Also known as: Overweight, unspecified | Overweight [NE60] Harmful effects of drugs, medicaments or biological substances, not elsewhere classified Also known as: Harmful effects of drugs, medicaments or biological substances, not elsewhere classified | drugs, medicaments or biological substances, toxicity not elsewhere classified | adverse drug effects | drug reaction NOS | drug allergy NOS Excludes: Alcohol intoxication | pathological drug intoxication | hypersensitivity reaction to correctly administered drug [MG43.1] Overeating Definition: The consumption of excess food in relation to energy and nutritional requirements. Also known as: Overeating | Excessive eating | gluttony | hyperalimentation | Hyperalimentation NOS Includes: Excessive eating Excludes: Bipolar or related disorders | Depressive disorders | Feeding or eating disorders === GRAPH WALKS === --- Walk 1 --- [CB40.2] Pulmonary collapse --EXCLUDES--> [?] Respiratory tuberculosis, confirmed Def: A disease of the respiratory tract, caused by an infection with the bacteria Mycobacterium tuberculosis, which has been confirmed by laboratory testing. This disease is characterised by chronic cough,... --CHILD--> [?] Tuberculosis of lung, confirmed histologically 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 confirmed histologically.... --- Walk 2 --- [CB40.2] Pulmonary collapse --EXCLUDES--> [?] Primary atelectasis of newborn Def: Failure of the lungs to expand after birth, as in stillborn infants or in liveborn infants who die before respiration is established... --PARENT--> [?] Respiratory disorders specific to the perinatal or neonatal period Def: A group of conditions occurring during the period of time around childbirth, especially the five months before and one month after birth which are associated with the cardiovascular or respiratory sys... --- Walk 3 --- [LA75.0] Accessory lobe of lung Def: An extra lobe of lung beyond the 3 on the right and the 2 on the left... --PARENT--> [LA75] Structural developmental anomalies of lungs Def: Any condition caused by failure of the lungs to correctly develop during the antenatal period.... --CHILD--> [LA75.2] Congenital hypoplasia of lung --- Walk 4 --- [LA75.0] Accessory lobe of lung Def: An extra lobe of lung beyond the 3 on the right and the 2 on the left... --PARENT--> [LA75] Structural developmental anomalies of lungs Def: Any condition caused by failure of the lungs to correctly develop during the antenatal period.... --CHILD--> [LA75.0] Accessory lobe of lung Def: An extra lobe of lung beyond the 3 on the right and the 2 on the left... --- Walk 5 --- [MD41] Clinical findings on diagnostic imaging of lung Def: 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 us... --PARENT--> [?] Clinical findings in the respiratory system --CHILD--> [MD42] Results of function studies of the respiratory system --- Walk 6 --- [MD41] Clinical findings on diagnostic imaging of lung Def: 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 us... --PARENT--> [?] Clinical findings in the respiratory system --PARENT--> [?] Symptoms, signs or clinical findings of the respiratory system
[ "[CB40.2] Pulmonary collapse\n --EXCLUDES--> [?] Respiratory tuberculosis, confirmed\n Def: A disease of the respiratory tract, caused by an infection with the bacteria Mycobacterium tuberculosis, which has been confirmed by laboratory testing. This disease is characterised by chronic cough,...\n --CHILD--> [?] Tuberculosis of lung, confirmed histologically\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 confirmed histologically....", "[CB40.2] Pulmonary collapse\n --EXCLUDES--> [?] Primary atelectasis of newborn\n Def: Failure of the lungs to expand after birth, as in stillborn infants or in liveborn infants who die before respiration is established...\n --PARENT--> [?] Respiratory disorders specific to the perinatal or neonatal period\n Def: A group of conditions occurring during the period of time around childbirth, especially the five months before and one month after birth which are associated with the cardiovascular or respiratory sys...", "[LA75.0] Accessory lobe of lung\n Def: An extra lobe of lung beyond the 3 on the right and the 2 on the left...\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--> [LA75.2] Congenital hypoplasia of lung", "[LA75.0] Accessory lobe of lung\n Def: An extra lobe of lung beyond the 3 on the right and the 2 on the left...\n --PARENT--> [LA75] Structural developmental anomalies of lungs\n Def: Any condition caused by failure of the lungs to correctly develop during the antenatal period....\n --CHILD--> [LA75.0] Accessory lobe of lung\n Def: An extra lobe of lung beyond the 3 on the right and the 2 on the left...", "[MD41] Clinical findings on diagnostic imaging of lung\n Def: 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 us...\n --PARENT--> [?] Clinical findings in the respiratory system\n --CHILD--> [MD42] Results of function studies of the respiratory system", "[MD41] Clinical findings on diagnostic imaging of lung\n Def: 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 us...\n --PARENT--> [?] Clinical findings in the respiratory system\n --PARENT--> [?] Symptoms, signs or clinical findings of the respiratory system" ]
CB40.2
Pulmonary collapse
[ { "from_icd11": "CB40.2", "icd10_code": "J9811", "icd10_title": "Atelectasis" }, { "from_icd11": "CB40.2", "icd10_code": "J9819", "icd10_title": "Other pulmonary collapse" }, { "from_icd11": "CB40.2", "icd10_code": "J981", "icd10_title": "Pulmonary collapse" }, { "from_icd11": "LA75.0", "icd10_code": "Q331", "icd10_title": "Accessory lobe of lung" }, { "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": "LA75.1", "icd10_code": "Q333", "icd10_title": "Agenesis of lung" }, { "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" } ]
J9811
Atelectasis
We present a case of characteristic ST-segment elevation suggestive of anteroseptal STEMI in a patient with no risk factors for coronary artery disease, a recently identified cardiac mass, and without any correlating symptoms. Our patient’s troponin T assay was found to be elevated above the 99th percentile of the upper reference limit on initial assessment without a subsequent rise and/or fall, and thus did not meet the criteria for myocardial infarction according to the Fourth Universal Definition of Myocardial Infarction . Given that the patient was a young, active-duty male (a patient population with a low risk for atherosclerotic coronary disease making STEMI highly unlikely), and that the clinical picture was not suggestive of an acute coronary syndrome (no symptoms of myocardial ischemia), the decision was made to forgo cardiac catheterization. With the time-sensitive and life-threatening nature of STEMIs, we believe this case illustrates the importance of maintaining a suspicion for alternative diagnoses when STEMI does not fit the clinical picture as the decision to begin anticoagulation and perform a left heart catheterization can place the patient at higher risk with less potential benefit in these scenarios. After much thought and discussion, we surmised that the ECG findings were most likely attributable to a persistent current of injury related to the interventricular septal mass.
4.082031
0.967773
sec[2]/p[0]
en
0.999997
33884235
https://doi.org/10.7759/cureus.13981
[ "stemi", "risk", "coronary", "myocardial", "that", "suggestive", "cardiac", "without", "infarction", "picture" ]
[ { "code": "BA41.0", "title": "Acute ST elevation myocardial infarction" }, { "code": "BA41.1", "title": "Acute non-ST elevation myocardial infarction" }, { "code": "BA42.0", "title": "Subsequent myocardial infarction, ST elevation myocardial infarction" }, { "code": "BA42.0&XA7RE3", "title": "Subsequent myocardial infarction, ST elevation myocardial infarction, anterior wall" }, { "code": "BA42.0&XA3RM8", "title": "Subsequent myocardial infarction, ST elevation myocardial infarction, inferior wall" }, { "code": "QC4Y", "title": "Personal history of other specified health problems" }, { "code": "QA43.Z", "title": "Supervision of high-risk pregnancy, unspecified" }, { "code": "QA43.Y", "title": "Other specified supervision of high-risk pregnancy" }, { "code": "QD84.Z", "title": "Occupational exposure to risk-factors, unspecified" }, { "code": "MB26.A", "title": "Suicidal ideation" } ]
=== ICD-11 CODES FOUND === [BA41.0] Acute ST elevation myocardial infarction Definition: ST elevation myocardial infarction (STEMI) is an acute myocardial infarction with developing ST elevation in two contiguous leads of the electrocardiogram. The criteria of ST elevation are as follows: New ST elevation at the J point in two contiguous leads where these cut points apply: 0.2mV in men > 40 years, > 0.25mV in men < 40 years, and > 0.15 mV in women. Also known as: Acute ST elevation myocardial infarction | Acute ST segment elevation myocardial infarction | STEMI - [ST elevation myocardial infarction] | ST elevation myocardial infarction | ST elevation MI [myocardial infarction] [BA41.1] Acute non-ST elevation myocardial infarction Also known as: Acute non-ST elevation myocardial infarction | Acute non ST segment elevation myocardial infarction | NSTEMI - [non ST elevation myocardial infarction] | non systolic time elevation myocardial infarction | non q wave myocardial infarction [BA42.0] Subsequent myocardial infarction, ST elevation myocardial infarction Definition: Extension or recurrent myocardial infarction. This category should be assigned for infarction of any myocardial site, occurring within 4 weeks (28 days) from onset of a previous infarction. This most commonly results from total occlusion of the culprit coronary artery. Also known as: Subsequent myocardial infarction, ST elevation myocardial infarction | subsequent ST segment elevation myocardial infarction | subsequent STEMI - [ST elevation myocardial infarction] | Subsequent myocardial infarction, ST elevation myocardial infarction, anterior wall | Subsequent STEMI, anterior wall [QC4Y] Personal history of other specified health problems Also known as: Personal history of other specified health problems | Personal history of diseases of the circulatory system | history of disease or disorder of circulatory system | personal history of conditions classifiable as diseases of the circulatory system | Personal history of diseases of the respiratory system [QA43.Z] Supervision of high-risk pregnancy, unspecified Also known as: Supervision of high-risk pregnancy, unspecified | Supervision of high-risk pregnancy [QA43.Y] Other specified supervision of high-risk pregnancy Also known as: Other specified supervision of high-risk pregnancy | Supervision of pregnancy with grand multiparity | pregnancy management affected by grand multiparity | multiparity affecting management of pregnancy, labour and delivery | pregnancy supervision for multiparity [QD84.Z] Occupational exposure to risk-factors, unspecified Also known as: Occupational exposure to risk-factors, unspecified | Occupational exposure to risk-factors | problem with occupational physical environment [MB26.A] Suicidal ideation Definition: Thoughts, ideas, or ruminations about the possibility of ending one's life, ranging from thinking that one would be better off dead to formulation of elaborate plans. Also known as: Suicidal ideation | suicidal tendency | suicidal tendencies | suicidal ideation tendencies | suicide risk Excludes: Suicide attempt | Personal history of self-harm === GRAPH WALKS === --- Walk 1 --- [BA41.0] Acute ST elevation myocardial infarction Def: ST elevation myocardial infarction (STEMI) is an acute myocardial infarction with developing ST elevation in two contiguous leads of the electrocardiogram. The criteria of ST elevation are as follows:... --PARENT--> [BA41] Acute myocardial infarction Def: The term acute myocardial infarction (MI) should be used when there is evidence of myocardial necrosis in a clinical setting consistent with acute myocardial ischemia. Under these conditions any one o... --EXCLUDES--> [?] Dressler syndrome Def: A condition of postmyocardial infarction (1 to 8 weeks), characterised by a set of associated symptom, including malaise, fever, pericardial discomfort, leukocytosis, an elevated sedimentation rate, a... --- Walk 2 --- [BA41.0] Acute ST elevation myocardial infarction Def: ST elevation myocardial infarction (STEMI) is an acute myocardial infarction with developing ST elevation in two contiguous leads of the electrocardiogram. The criteria of ST elevation are as follows:... --PARENT--> [BA41] Acute myocardial infarction Def: The term acute myocardial infarction (MI) should be used when there is evidence of myocardial necrosis in a clinical setting consistent with acute myocardial ischemia. Under these conditions any one o... --PARENT--> [?] Acute ischaemic heart disease --- Walk 3 --- [BA41.1] Acute non-ST elevation myocardial infarction --PARENT--> [BA41] Acute myocardial infarction Def: The term acute myocardial infarction (MI) should be used when there is evidence of myocardial necrosis in a clinical setting consistent with acute myocardial ischemia. Under these conditions any one o... --PARENT--> [?] Acute ischaemic heart disease --- Walk 4 --- [BA41.1] Acute non-ST elevation myocardial infarction --PARENT--> [BA41] Acute myocardial infarction Def: The term acute myocardial infarction (MI) should be used when there is evidence of myocardial necrosis in a clinical setting consistent with acute myocardial ischemia. Under these conditions any one o... --EXCLUDES--> [?] Certain current complications following acute myocardial infarction Def: Secondary conditions which may occur in the course after the heart attack. They include pericarditis, arrhythmia, cardiogenic shock, heart failure, ventricular rupture, ventricular aneurysm (with thro... --- Walk 5 --- [BA42.0] Subsequent myocardial infarction, ST elevation myocardial infarction Def: Extension or recurrent myocardial infarction. This category should be assigned for infarction of any myocardial site, occurring within 4 weeks (28 days) from onset of a previous infarction. This most ... --PARENT--> [BA42] Subsequent myocardial infarction Def: Infarction of any myocardial site, occurring within 4 weeks (28 days) from onset of a previous infarction... --CHILD--> [BA42.1] Subsequent myocardial infarction, non-ST elevation myocardial infarction Def: Extension or recurrent myocardial infarction. For morbidity coding, this category should be assigned for infarction of any myocardial site, occurring within 4 weeks (28 days) from onset of a previous ... --- Walk 6 --- [BA42.0] Subsequent myocardial infarction, ST elevation myocardial infarction Def: Extension or recurrent myocardial infarction. This category should be assigned for infarction of any myocardial site, occurring within 4 weeks (28 days) from onset of a previous infarction. This most ... --PARENT--> [BA42] Subsequent myocardial infarction Def: Infarction of any myocardial site, occurring within 4 weeks (28 days) from onset of a previous infarction... --CHILD--> [BA42.Z] Subsequent myocardial infarction, unspecified
[ "[BA41.0] Acute ST elevation myocardial infarction\n Def: ST elevation myocardial infarction (STEMI) is an acute myocardial infarction with developing ST elevation in two contiguous leads of the electrocardiogram. The criteria of ST elevation are as follows:...\n --PARENT--> [BA41] Acute myocardial infarction\n Def: The term acute myocardial infarction (MI) should be used when there is evidence of myocardial necrosis in a clinical setting consistent with acute myocardial ischemia. Under these conditions any one o...\n --EXCLUDES--> [?] Dressler syndrome\n Def: A condition of postmyocardial infarction (1 to 8 weeks), characterised by a set of associated symptom, including malaise, fever, pericardial discomfort, leukocytosis, an elevated sedimentation rate, a...", "[BA41.0] Acute ST elevation myocardial infarction\n Def: ST elevation myocardial infarction (STEMI) is an acute myocardial infarction with developing ST elevation in two contiguous leads of the electrocardiogram. The criteria of ST elevation are as follows:...\n --PARENT--> [BA41] Acute myocardial infarction\n Def: The term acute myocardial infarction (MI) should be used when there is evidence of myocardial necrosis in a clinical setting consistent with acute myocardial ischemia. Under these conditions any one o...\n --PARENT--> [?] Acute ischaemic heart disease", "[BA41.1] Acute non-ST elevation myocardial infarction\n --PARENT--> [BA41] Acute myocardial infarction\n Def: The term acute myocardial infarction (MI) should be used when there is evidence of myocardial necrosis in a clinical setting consistent with acute myocardial ischemia. Under these conditions any one o...\n --PARENT--> [?] Acute ischaemic heart disease", "[BA41.1] Acute non-ST elevation myocardial infarction\n --PARENT--> [BA41] Acute myocardial infarction\n Def: The term acute myocardial infarction (MI) should be used when there is evidence of myocardial necrosis in a clinical setting consistent with acute myocardial ischemia. Under these conditions any one o...\n --EXCLUDES--> [?] Certain current complications following acute myocardial infarction\n Def: Secondary conditions which may occur in the course after the heart attack. They include pericarditis, arrhythmia, cardiogenic shock, heart failure, ventricular rupture, ventricular aneurysm (with thro...", "[BA42.0] Subsequent myocardial infarction, ST elevation myocardial infarction\n Def: Extension or recurrent myocardial infarction. This category should be assigned for infarction of any myocardial site, occurring within 4 weeks (28 days) from onset of a previous infarction. This most ...\n --PARENT--> [BA42] Subsequent myocardial infarction\n Def: Infarction of any myocardial site, occurring within 4 weeks (28 days) from onset of a previous infarction...\n --CHILD--> [BA42.1] Subsequent myocardial infarction, non-ST elevation myocardial infarction\n Def: Extension or recurrent myocardial infarction. For morbidity coding, this category should be assigned for infarction of any myocardial site, occurring within 4 weeks (28 days) from onset of a previous ...", "[BA42.0] Subsequent myocardial infarction, ST elevation myocardial infarction\n Def: Extension or recurrent myocardial infarction. This category should be assigned for infarction of any myocardial site, occurring within 4 weeks (28 days) from onset of a previous infarction. This most ...\n --PARENT--> [BA42] Subsequent myocardial infarction\n Def: Infarction of any myocardial site, occurring within 4 weeks (28 days) from onset of a previous infarction...\n --CHILD--> [BA42.Z] Subsequent myocardial infarction, unspecified" ]
BA41.0
Acute ST elevation myocardial infarction
[ { "from_icd11": "BA41.0", "icd10_code": "I2109", "icd10_title": "ST elevation (STEMI) myocardial infarction involving other coronary artery of anterior wall" }, { "from_icd11": "BA41.0", "icd10_code": "I2119", "icd10_title": "ST elevation (STEMI) myocardial infarction involving other coronary artery of inferior wall" }, { "from_icd11": "BA41.0", "icd10_code": "I2111", "icd10_title": "ST elevation (STEMI) myocardial infarction involving right coronary artery" }, { "from_icd11": "BA41.0", "icd10_code": "I2102", "icd10_title": "ST elevation (STEMI) myocardial infarction involving left anterior descending coronary artery" }, { "from_icd11": "BA41.0", "icd10_code": "I2101", "icd10_title": "ST elevation (STEMI) myocardial infarction involving left main coronary artery" }, { "from_icd11": "BA41.0", "icd10_code": "I210", "icd10_title": "ST elevation (STEMI) myocardial infarction of anterior wall" }, { "from_icd11": "BA41.0", "icd10_code": "I211", "icd10_title": "ST elevation (STEMI) myocardial infarction of inferior wall" }, { "from_icd11": "BA41.1", "icd10_code": "I214", "icd10_title": "Non-ST elevation (NSTEMI) myocardial infarction" }, { "from_icd11": "QC4Y", "icd10_code": "Z86718", "icd10_title": "Personal history of other venous thrombosis and embolism" }, { "from_icd11": "QC4Y", "icd10_code": "Z9181", "icd10_title": "History of falling" }, { "from_icd11": "QA43.Z", "icd10_code": "Z35", "icd10_title": "" }, { "from_icd11": "QA43.Z", "icd10_code": "Z354", "icd10_title": "" }, { "from_icd11": "QA43.Z", "icd10_code": "Z358", "icd10_title": "" }, { "from_icd11": "QA43.Z", "icd10_code": "Z359", "icd10_title": "" }, { "from_icd11": "QA43.Z", "icd10_code": "O0990 ", "icd10_title": "" } ]
I2109
ST elevation (STEMI) myocardial infarction involving other coronary artery of anterior wall
This is an example. A 66-year-old man with 1.8 cm sporadic RET negative MTC underwent surgery. Pathology showed many microscopic lymph node metastases. Preoperative calcitonin at 3800 pg/ml decreased to 190 pg/ml postoperatively, indicating he had BPD. How do you predict the prognosis of the patient? Pathological node metastases and persistent disease. Poor prognosis? With the resected tumor weight, preoperative and postoperative calcitonin values, the residual tumor weight was calculated to be 0.18 g. The number ( β ) of doublings for this tumor to reach 1000 g was 12.4. Calcitonin DT was widely distributed in 45 patients with MTC treated at Kuma Hospital who had BPD postoperatively . Most of the patients had calcitonin DT of longer than 4 years. If his calcitonin DT was 4 years, the expected survival was calculated to be 49 years. If 1000 g seems too big, you can set the host-killing tumor size to 100 g. In this setting, β is 9.1 and the expected survival is 36 years. The actual calcitonin DT calculated 3 years after surgery was 5.6 years. I can say that this patient will not die of MTC although he has persistent disease. I said to the patient, “Don’t worry too much, you will live for long time.” Fig. 3 Distribution according to calcitonin doubling time of 45 patients with medullary thyroid carcinoma who underwent surgery at Kuma Hospital and had persistent hypercalcitoninemia postoperatively
3.869141
0.583984
sec[1]/p[3]
en
0.999997
36153411
https://doi.org/10.1007/s00268-022-06741-4
[ "calcitonin", "this", "tumor", "postoperatively", "persistent", "calculated", "patients", "node", "metastases", "preoperative" ]
[ { "code": "5A04", "title": "Hypersecretion of calcitonin" }, { "code": "4A01.03", "title": "Transient hypogammaglobulinaemia of infancy" }, { "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": "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" } ]
=== ICD-11 CODES FOUND === [5A04] Hypersecretion of calcitonin Definition: This is the process of elaborating, releasing, and oozing a 32-amino acid linear polypeptide hormone that is produced in humans primarily by the parafollicular cells (also known as C-cells) of the thyroid, and in many other animals in the ultimobranchial body. Also known as: Hypersecretion of calcitonin | Hypersecretion of thyrocalcitonin | C-cell hyperplasia of thyroid Includes: Hypersecretion of thyrocalcitonin | C-cell hyperplasia of thyroid [4A01.03] Transient hypogammaglobulinaemia of infancy Also known as: Transient hypogammaglobulinaemia of infancy | immunoglobulin maturational delay | THI - [transient hypogammaglobulinaemia of infancy] [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 [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 === GRAPH WALKS === --- Walk 1 --- [5A04] Hypersecretion of calcitonin Def: This is the process of elaborating, releasing, and oozing a 32-amino acid linear polypeptide hormone that is produced in humans primarily by the parafollicular cells (also known as C-cells) of the thy... --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.... --CHILD--> [5A01] Nontoxic goitre Def: Enlargement of the thyroid gland due to follicular multiplication, unaccompanied by hyperthyroidism or thyrotoxicosis... --- Walk 2 --- [5A04] Hypersecretion of calcitonin Def: This is the process of elaborating, releasing, and oozing a 32-amino acid linear polypeptide hormone that is produced in humans primarily by the parafollicular cells (also known as C-cells) of the thy... --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.... --CHILD--> [5A02] Thyrotoxicosis Def: A hypermetabolic condition associated with elevated levels of free thyroxine and/or free triiodothyronine resulting in excess synthesis and secretion of thyroid hormone... --- Walk 3 --- [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 4 --- [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 5 --- [2F9Z] Neoplasms of unknown behaviour of unspecified site --PARENT--> [?] Neoplasms of unknown behaviour, except of lymphoid, haematopoietic, central nervous system or related tissues --CHILD--> [2F91] Neoplasms of unknown behaviour of middle ear, respiratory or intrathoracic organs --- Walk 6 --- [2F9Z] Neoplasms of unknown behaviour of unspecified site --PARENT--> [?] Neoplasms of unknown behaviour, except of lymphoid, haematopoietic, central nervous system or related tissues --CHILD--> [2F91] Neoplasms of unknown behaviour of middle ear, respiratory or intrathoracic organs
[ "[5A04] Hypersecretion of calcitonin\n Def: This is the process of elaborating, releasing, and oozing a 32-amino acid linear polypeptide hormone that is produced in humans primarily by the parafollicular cells (also known as C-cells) of the thy...\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....\n --CHILD--> [5A01] Nontoxic goitre\n Def: Enlargement of the thyroid gland due to follicular multiplication, unaccompanied by hyperthyroidism or thyrotoxicosis...", "[5A04] Hypersecretion of calcitonin\n Def: This is the process of elaborating, releasing, and oozing a 32-amino acid linear polypeptide hormone that is produced in humans primarily by the parafollicular cells (also known as C-cells) of the thy...\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....\n --CHILD--> [5A02] Thyrotoxicosis\n Def: A hypermetabolic condition associated with elevated levels of free thyroxine and/or free triiodothyronine resulting in excess synthesis and secretion of thyroid hormone...", "[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...", "[2F9Z] Neoplasms of unknown behaviour of unspecified site\n --PARENT--> [?] Neoplasms of unknown behaviour, except of lymphoid, haematopoietic, central nervous system or related tissues\n --CHILD--> [2F91] Neoplasms of unknown behaviour of middle ear, respiratory or intrathoracic organs", "[2F9Z] Neoplasms of unknown behaviour of unspecified site\n --PARENT--> [?] Neoplasms of unknown behaviour, except of lymphoid, haematopoietic, central nervous system or related tissues\n --CHILD--> [2F91] Neoplasms of unknown behaviour of middle ear, respiratory or intrathoracic organs" ]
5A04
Hypersecretion of calcitonin
[ { "from_icd11": "5A04", "icd10_code": "E070", "icd10_title": "Hypersecretion of calcitonin" }, { "from_icd11": "4A01.03", "icd10_code": "D807", "icd10_title": "Transient hypogammaglobulinemia of infancy" }, { "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" } ]
E070
Hypersecretion of calcitonin
Due to our high suspicion of HSV encephalitis in our patient, we analyze the current literature regarding the potential causes that could have yielded a negative PCR test. Some investigators believe that 1% to 5% of CSF specimens might contain inhibitors that interfere with PCR . For example, a high concentration of porphyrin compounds, which can be derived from the hemolysis of red blood cells, can interfere with PCR reactions . Other explanations for a negative PCR test include the PCR being sent during the first 4 days of neurological symptoms, the viral load being too low for detection, or the CSF sample being too low in volume . Low CSF cell counts, location of the infection in the CNS, sample dilution, and variation in primers used during PCR processing have also been suggested as the cause for false-negative results . Negative PCR tests tend to also be associated with low CSF protein and leukocyte counts . However, our case demonstrates an atypical presentation with high CSF glucose and protein with normal leukocyte counts. Additionally, our case is unique in the regard that the patient had reportedly been suffering from mild neurologic symptoms for ten days prior to the ED admission. We argue that the admission CSF analysis would’ve yielded a positive result for HSV based on the timeline that the CSF was collected after 72 hours since the onset of neurological symptoms due to infection.
4.128906
0.575684
sec[2]/p[1]
en
0.999995
PMC9980281
https://doi.org/10.7759/cureus.34448
[ "that", "counts", "yielded", "interfere", "neurological", "sample", "infection", "protein", "leukocyte", "suspicion" ]
[ { "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": "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 === [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 [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 --- [8A80.Z] Migraine, unspecified --PARENT--> [8A80] Migraine Def: A primary headache disorder, in most cases episodic. Disabling attacks lasting 4-72 hours are characterised by moderate or severe headache, usually accompanied by nausea, vomiting and/or photophobia a... --CHILD--> [8A80.0] Migraine without aura Def: Recurrent headache disorder manifesting in attacks lasting 4-72 hours. The duration of attacks may be shorter in children. Typical characteristics of the headache are unilateral location, pulsating qu... --- Walk 2 --- [8A80.Z] Migraine, unspecified --PARENT--> [8A80] Migraine Def: A primary headache disorder, in most cases episodic. Disabling attacks lasting 4-72 hours are characterised by moderate or severe headache, usually accompanied by nausea, vomiting and/or photophobia a... --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.... --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 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--> [PL13.2] Drug-related injury or harm in the context of correct administration or dosage, as mode of injury or harm --- Walk 6 --- [PL13.6] Medication or substance that is known to be an allergen, as mode of injury or harm --PARENT--> [PL13] Mode of injury or harm associated with exposure to a drug, medicament or biological substance --CHILD--> [PL13.2] Drug-related injury or harm in the context of correct administration or dosage, as mode of injury or harm
[ "[8A80.Z] Migraine, unspecified\n --PARENT--> [8A80] Migraine\n Def: A primary headache disorder, in most cases episodic. Disabling attacks lasting 4-72 hours are characterised by moderate or severe headache, usually accompanied by nausea, vomiting and/or photophobia a...\n --CHILD--> [8A80.0] Migraine without aura\n Def: Recurrent headache disorder manifesting in attacks lasting 4-72 hours. The duration of attacks may be shorter in children. Typical characteristics of the headache are unilateral location, pulsating qu...", "[8A80.Z] Migraine, unspecified\n --PARENT--> [8A80] Migraine\n Def: A primary headache disorder, in most cases episodic. Disabling attacks lasting 4-72 hours are characterised by moderate or severe headache, usually accompanied by nausea, vomiting and/or photophobia a...\n --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 --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", "[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--> [PL13.2] Drug-related injury or harm in the context of correct administration or dosage, as mode of injury or harm", "[PL13.6] Medication or substance that is known to be an allergen, as mode of injury or harm\n --PARENT--> [PL13] Mode of injury or harm associated with exposure to a drug, medicament or biological substance\n --CHILD--> [PL13.2] Drug-related injury or harm in the context of correct administration or dosage, as mode of injury or harm" ]
8A80.Z
Migraine, unspecified
[ { "from_icd11": "8A80.Z", "icd10_code": "G43B0", "icd10_title": "Ophthalmoplegic migraine, not intractable" }, { "from_icd11": "8A80.Z", "icd10_code": "G43409", "icd10_title": "Hemiplegic migraine, not intractable, without status migrainosus" }, { "from_icd11": "8A80.Z", "icd10_code": "G43A0", "icd10_title": "Cyclical vomiting, in migraine, not intractable" }, { "from_icd11": "8A80.Z", "icd10_code": "G43D0", "icd10_title": "Abdominal migraine, not intractable" }, { "from_icd11": "8A80.Z", "icd10_code": "G43709", "icd10_title": "Chronic migraine without aura, not intractable, without status migrainosus" }, { "from_icd11": "8A80.Z", "icd10_code": "G43A1", "icd10_title": "Cyclical vomiting, in migraine, intractable" }, { "from_icd11": "8A80.Z", "icd10_code": "G43509", "icd10_title": "Persistent migraine aura without cerebral infarction, not intractable, without status migrainosus" }, { "from_icd11": "8A80.Z", "icd10_code": "G43719", "icd10_title": "Chronic migraine without aura, intractable, without status migrainosus" }, { "from_icd11": "8A80.Z", "icd10_code": "G43501", "icd10_title": "Persistent migraine aura without cerebral infarction, not intractable, with status migrainosus" }, { "from_icd11": "8A80.Z", "icd10_code": "G43C0", "icd10_title": "Periodic headache syndromes in child or adult, not intractable" }, { "from_icd11": "8A80.Z", "icd10_code": "G43401", "icd10_title": "Hemiplegic migraine, not intractable, with status migrainosus" }, { "from_icd11": "8A80.Z", "icd10_code": "G43419", "icd10_title": "Hemiplegic migraine, intractable, without status migrainosus" }, { "from_icd11": "8A80.Z", "icd10_code": "G43B1", "icd10_title": "Ophthalmoplegic migraine, intractable" }, { "from_icd11": "8A80.Z", "icd10_code": "G43C1", "icd10_title": "Periodic headache syndromes in child or adult, intractable" }, { "from_icd11": "8A80.Z", "icd10_code": "G43D1", "icd10_title": "Abdominal migraine, intractable" } ]
G43B0
Ophthalmoplegic migraine, not intractable
The proportion of bacterial infections in adult HLH is very small, and most of them are related to tuberculosis ( 4 ). In this case report, Klebsiella pneumoniae is a rare factor for secondary HLH, which has been reported only a few times ( 5 ). Klebsiella pneumoniae is a common opportunistic pathogen, when the host’s immune capacity decreases it can induce infection and abscesses in many locations. We know from some case reports that Klebsiella pneumoniae can cause a psoas abscess and spinal infection, and, in addition, patients with psoas abscesses usually have fever and back or hip pain, but both are very rare ( 6 , 7 ). Because of the following reasons, the possibility of abscesses caused by other reasons (such as autoantibodies against IL-12 or insufficient haploid function of GATA2) was minimal. First, the patient had been treated with meropenem before the second admission, all indicators improved, and the blood culture was negative when he was re-admitted. Second, it is almost impossible for patients to infect other bacteria outside the hospital. Third, the patient had no discomfort after abscess drainage. Thus, we concluded that it had been caused by the initial spread of Klebsiella pneumoniae , resulting in bilateral psoas abscesses and intraspinal abscess, but not relapse or aggravation of HLH. This suggested that, initially, the patient had HLH associated with Klebsiella pneumoniae .
4.007813
0.84375
sec[2]/p[0]
en
0.999998
34335586
https://doi.org/10.3389/fimmu.2021.684805
[ "klebsiella", "pneumoniae", "abscesses", "that", "psoas", "abscess", "this", "rare", "infection", "patients" ]
[ { "code": "CA40.03", "title": "Pneumonia due to Klebsiella pneumoniae" }, { "code": "1C4Y", "title": "Other specified bacterial diseases" }, { "code": "1A0Y&XN7WL", "title": "Colitis due to Klebsiella oxytoca" }, { "code": "MG50.55", "title": "Polymyxin resistant Klebsiella pneumoniae" }, { "code": "MG50.51", "title": "Fluoroquinolone resistant Klebsiella pneumoniae" }, { "code": "CA40.Z", "title": "Pneumonia, organism unspecified" }, { "code": "CA40.Y", "title": "Other specified pneumonia" }, { "code": "KB24", "title": "Congenital pneumonia" }, { "code": "CA40.1Z", "title": "Viral pneumonia, unspecified" }, { "code": "CA40.0Z", "title": "Bacterial pneumonia, unspecified" } ]
=== ICD-11 CODES FOUND === [CA40.03] Pneumonia due to Klebsiella pneumoniae Definition: A disease of the pulmonary system, caused by an infection with the gram-negative bacteria Klebsiella pneumoniae. This infection common presents with thick, haemorrhagic, mucoid sputum. Transmission is by inhalation of infected respiratory secretions. Confirmation is by identification of Klebsiella pneumoniae in a sputum sample. Also known as: Pneumonia due to Klebsiella pneumoniae | klebsiella lobar pneumonia [1C4Y] Other specified bacterial diseases Also known as: Other specified bacterial diseases | Non-venereal treponematoses | Other spirochaetal diseases | spirochetal infection, nec | spirochetosis [MG50.55] Polymyxin resistant Klebsiella pneumoniae Also known as: Polymyxin resistant Klebsiella pneumoniae | Colistin resistant Klebsiella pneumoniae [MG50.51] Fluoroquinolone resistant Klebsiella pneumoniae Also known as: Fluoroquinolone resistant Klebsiella pneumoniae | Ciprofloxacin resistant Klebsiella pneumoniae | Levofloxacin resistant Klebsiella pneumoniae [CA40.Z] Pneumonia, organism unspecified Also known as: Pneumonia, organism unspecified | Pneumonia | infectious pneumonia | PN - [pneumonia] | lobar pneumonia NOS [CA40.Y] Other specified pneumonia Also known as: Other specified pneumonia | Pneumonia in parasitic diseases | Late acquired pneumonia | Late-onset pneumonia due to other organisms | Pleuropneumonia [KB24] Congenital pneumonia Definition: Congenital pneumonia is an acute respiratory infection contracted prenatally or during the intrapartum period that is caused by a virus, bacteria, or fungi. Also known as: Congenital pneumonia | acute congenital pneumonia | congenital double pneumonia | congenital purulent pneumonia | congenital infective pneumonia Includes: infective pneumonia acquired in utero or during birth Excludes: Neonatal aspiration syndromes | Pneumonitis [CA40.1Z] Viral pneumonia, unspecified Also known as: Viral pneumonia, unspecified | Viral pneumonia | acute viral pneumonia | bronchopneumonia due to viruses other than influenza viruses | interstitial viral pneumonia [CA40.0Z] Bacterial pneumonia, unspecified Also known as: Bacterial pneumonia, unspecified | Bacterial pneumonia | acute bacillus pneumonia | acute bacterial pneumonia | bacillus double pneumonia === GRAPH WALKS === --- Walk 1 --- [CA40.03] Pneumonia due to Klebsiella pneumoniae Def: A disease of the pulmonary system, caused by an infection with the gram-negative bacteria Klebsiella pneumoniae. This infection common presents with thick, haemorrhagic, mucoid sputum. Transmission is... --PARENT--> [CA40.0] Bacterial pneumonia Def: A disease of the pulmonary system, caused by an infection with a bacterial source. This disease is characterised by fever, lethargy, headache, myalgia, vomiting, or coughing. Transmission is by inhala... --EXCLUDES--> [?] Congenital pneumonia Def: Congenital pneumonia is an acute respiratory infection contracted prenatally or during the intrapartum period that is caused by a virus, bacteria, or fungi.... --- Walk 2 --- [CA40.03] Pneumonia due to Klebsiella pneumoniae Def: A disease of the pulmonary system, caused by an infection with the gram-negative bacteria Klebsiella pneumoniae. This infection common presents with thick, haemorrhagic, mucoid sputum. Transmission is... --PARENT--> [CA40.0] Bacterial pneumonia Def: A disease of the pulmonary system, caused by an infection with a bacterial source. This disease is characterised by fever, lethargy, headache, myalgia, vomiting, or coughing. Transmission is by inhala... --RELATED_TO--> [?] Pulmonary actinomycosis Def: This is a pulmonary infectious bacterial disease caused by Actinomyces species such as Actinomyces israelii or A. gerencseriae. It can also be caused by Propionibacterium propionicus, and the conditio... --- Walk 3 --- [1C4Y] Other specified bacterial diseases --PARENT--> [?] Other bacterial diseases --CHILD--> [1C11] Bartonellosis Def: Any infection caused by the gram-negative bacteria Bartonella.... --- Walk 4 --- [1C4Y] Other specified bacterial diseases --PARENT--> [?] Other bacterial diseases --CHILD--> [1C12] Whooping cough Def: A disease of the upper respiratory tract, caused by an infection with the gram-negative bacteria Bordetella. This disease typically presents with paroxysmal cough, inspiratory whoop, and fainting or v... --- Walk 5 --- [MG50.55] Polymyxin resistant Klebsiella pneumoniae --PARENT--> [MG50.5] Antibiotic resistant Klebsiella pneumoniae --CHILD--> [MG50.51] Fluoroquinolone resistant Klebsiella pneumoniae --- Walk 6 --- [MG50.55] Polymyxin resistant Klebsiella pneumoniae --PARENT--> [MG50.5] Antibiotic resistant Klebsiella pneumoniae --PARENT--> [MG50] Finding of gram negative bacteria resistant to antimicrobial drugs
[ "[CA40.03] Pneumonia due to Klebsiella pneumoniae\n Def: A disease of the pulmonary system, caused by an infection with the gram-negative bacteria Klebsiella pneumoniae. This infection common presents with thick, haemorrhagic, mucoid sputum. Transmission is...\n --PARENT--> [CA40.0] Bacterial pneumonia\n Def: A disease of the pulmonary system, caused by an infection with a bacterial source. This disease is characterised by fever, lethargy, headache, myalgia, vomiting, or coughing. Transmission is by inhala...\n --EXCLUDES--> [?] Congenital pneumonia\n Def: Congenital pneumonia is an acute respiratory infection contracted prenatally or during the intrapartum period that is caused by a virus, bacteria, or fungi....", "[CA40.03] Pneumonia due to Klebsiella pneumoniae\n Def: A disease of the pulmonary system, caused by an infection with the gram-negative bacteria Klebsiella pneumoniae. This infection common presents with thick, haemorrhagic, mucoid sputum. Transmission is...\n --PARENT--> [CA40.0] Bacterial pneumonia\n Def: A disease of the pulmonary system, caused by an infection with a bacterial source. This disease is characterised by fever, lethargy, headache, myalgia, vomiting, or coughing. Transmission is by inhala...\n --RELATED_TO--> [?] Pulmonary actinomycosis\n Def: This is a pulmonary infectious bacterial disease caused by Actinomyces species such as Actinomyces israelii or A. gerencseriae. It can also be caused by Propionibacterium propionicus, and the conditio...", "[1C4Y] Other specified bacterial diseases\n --PARENT--> [?] Other bacterial diseases\n --CHILD--> [1C11] Bartonellosis\n Def: Any infection caused by the gram-negative bacteria Bartonella....", "[1C4Y] Other specified bacterial diseases\n --PARENT--> [?] Other bacterial diseases\n --CHILD--> [1C12] Whooping cough\n Def: A disease of the upper respiratory tract, caused by an infection with the gram-negative bacteria Bordetella. This disease typically presents with paroxysmal cough, inspiratory whoop, and fainting or v...", "[MG50.55] Polymyxin resistant Klebsiella pneumoniae\n --PARENT--> [MG50.5] Antibiotic resistant Klebsiella pneumoniae\n --CHILD--> [MG50.51] Fluoroquinolone resistant Klebsiella pneumoniae", "[MG50.55] Polymyxin resistant Klebsiella pneumoniae\n --PARENT--> [MG50.5] Antibiotic resistant Klebsiella pneumoniae\n --PARENT--> [MG50] Finding of gram negative bacteria resistant to antimicrobial drugs" ]
CA40.03
Pneumonia due to Klebsiella pneumoniae
[ { "from_icd11": "CA40.03", "icd10_code": "J150", "icd10_title": "Pneumonia due to Klebsiella pneumoniae" }, { "from_icd11": "1C4Y", "icd10_code": "B9689", "icd10_title": "Other specified bacterial agents as the cause of diseases classified elsewhere" }, { "from_icd11": "MG50.55", "icd10_code": "U838", "icd10_title": "" }, { "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" } ]
J150
Pneumonia due to Klebsiella pneumoniae
The exact time length of reversible retinal hypoxic damage is unknown yet and it is estimated between 4.5 and 12 h . Intravenous tissue plasminogen activator (tPA) is an evidence-based therapy for AIS, when provided within 4.5 h . Treatment with tPA showed a strong effect even in patients with CRAO , however adequate randomized clinical trials are still ongoing . In centers where endovascular therapy is performed, intra-arterial tPA (Ia-tPA) may be considered an alternative treatment, and the time window for drug administration is potentially increased . Regretfully, although prompt management of acute CRAO is mandatory to maximize visual outcome and avoid any secondary ischemic event, a unanimous consensus on the topic has not been reached yet. Our child did not receive a thrombolytic treatment due to the late diagnosis, whereas anticoagulant therapy was soon administered. Several non-invasive treatments have been proposed and tried in some adult cases ; however these strategies are not uniformly supported by the current scientific literature, since there is no evidence of effectiveness . In order to improve retinal oedema, and bearing in mind the known inflammatory and vasculitis tendency of SARS-CoV-2 infection, iv and oral steroids were administered to our patient, nonetheless with poor visual outcome, in accordance to other adult cases in the literature and to the known prognosis of CRAO .
4.246094
0.86084
sec[2]/p[6]
en
0.999998
37704960
https://doi.org/10.1186/s12887-023-04276-8
[ "crao", "time", "retinal", "evidence", "however", "visual", "outcome", "cases", "literature", "known" ]
[ { "code": "9B74.0", "title": "Retinal artery occlusions" }, { "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": "9B7Z", "title": "Disorders of the retina, unspecified" }, { "code": "9B74.Z", "title": "Retinal vascular occlusions, unspecified" }, { "code": "9B73.4", "title": "Retinal breaks without detachment" }, { "code": "9B78.9", "title": "Retinal atrophy" } ]
=== ICD-11 CODES FOUND === [9B74.0] Retinal artery occlusions Also known as: Retinal artery occlusions | retina artery narrowing | retinal artery spasm | spasm of ophthalmic artery | retinal spasm Includes: Retinal artery branch occlusion [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 [9B7Z] Disorders of the retina, unspecified Also known as: Disorders of the retina, unspecified | retinal disease | retinal lesion NOS [9B74.Z] Retinal vascular occlusions, unspecified Also known as: Retinal vascular occlusions, unspecified | Retinal vascular occlusions | occlusion of retinal vessels | retinal obstruction [9B73.4] Retinal breaks without detachment Also known as: Retinal breaks without detachment | Retinal break NOS | ruptured retina | Horseshoe tear of retina without detachment | Round hole of retina without detachment Includes: Horseshoe tear of retina without detachment | Round hole of retina without detachment Excludes: Chorioretinal scars after surgery for detachment | peripheral retinal degeneration without break [9B78.9] Retinal atrophy Definition: This is a group of genetic diseases and is characterised by the bilateral degeneration of the retina, causing progressive vision loss culminating in blindness. Also known as: Retinal atrophy | atrophic retina === GRAPH WALKS === --- Walk 1 --- [9B74.0] Retinal artery occlusions --PARENT--> [9B74] Retinal vascular occlusions Def: These are obstruction or closure of retinal vascular structures.... --EXCLUDES--> [?] Transient visual loss --- Walk 2 --- [9B74.0] Retinal artery occlusions --PARENT--> [9B74] Retinal vascular occlusions Def: These are obstruction or closure of retinal vascular structures.... --CHILD--> [9B74.2] Combined retinal arterial and vein occlusion --- Walk 3 --- [PL13.52] Incorrect timing of drug or medicament, as mode of injury --EXCLUDES--> [?] Delayed treatment --CHILD--> [?] Problem associated with delayed administration of a needed medication --- Walk 4 --- [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 5 --- [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--> [QF20] Difficulty or need for assistance with learning --- Walk 6 --- [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
[ "[9B74.0] Retinal artery occlusions\n --PARENT--> [9B74] Retinal vascular occlusions\n Def: These are obstruction or closure of retinal vascular structures....\n --EXCLUDES--> [?] Transient visual loss", "[9B74.0] Retinal artery occlusions\n --PARENT--> [9B74] Retinal vascular occlusions\n Def: These are obstruction or closure of retinal vascular structures....\n --CHILD--> [9B74.2] Combined retinal arterial and vein occlusion", "[PL13.52] Incorrect timing of drug or medicament, as mode of injury\n --EXCLUDES--> [?] Delayed treatment\n --CHILD--> [?] Problem associated with delayed administration of a needed medication", "[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", "[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--> [QF20] Difficulty or need for assistance with learning", "[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" ]
9B74.0
Retinal artery occlusions
[ { "from_icd11": "9B74.0", "icd10_code": "H34239", "icd10_title": "Retinal artery branch occlusion, unspecified eye" }, { "from_icd11": "9B74.0", "icd10_code": "H3401", "icd10_title": "Transient retinal artery occlusion, right eye" }, { "from_icd11": "9B74.0", "icd10_code": "H34231", "icd10_title": "Retinal artery branch occlusion, right eye" }, { "from_icd11": "9B74.0", "icd10_code": "H3412", "icd10_title": "Central retinal artery occlusion, left eye" }, { "from_icd11": "9B74.0", "icd10_code": "H3402", "icd10_title": "Transient retinal artery occlusion, left eye" }, { "from_icd11": "9B74.0", "icd10_code": "H34232", "icd10_title": "Retinal artery branch occlusion, left eye" }, { "from_icd11": "9B74.0", "icd10_code": "H34211", "icd10_title": "Partial retinal artery occlusion, right eye" }, { "from_icd11": "9B74.0", "icd10_code": "H3411", "icd10_title": "Central retinal artery occlusion, right eye" }, { "from_icd11": "9B74.0", "icd10_code": "H34212", "icd10_title": "Partial retinal artery occlusion, left eye" }, { "from_icd11": "9B74.0", "icd10_code": "H3410", "icd10_title": "Central retinal artery occlusion, unspecified eye" }, { "from_icd11": "9B74.0", "icd10_code": "H3400", "icd10_title": "Transient retinal artery occlusion, unspecified eye" }, { "from_icd11": "9B74.0", "icd10_code": "H34219", "icd10_title": "Partial retinal artery occlusion, unspecified eye" }, { "from_icd11": "9B74.0", "icd10_code": "H3413", "icd10_title": "Central retinal artery occlusion, bilateral" }, { "from_icd11": "9B74.0", "icd10_code": "H340", "icd10_title": "Transient retinal artery occlusion" }, { "from_icd11": "9B74.0", "icd10_code": "H341", "icd10_title": "Central retinal artery occlusion" } ]
H34239
Retinal artery branch occlusion, unspecified eye
New-onset therapy refractory status epilepticus (NORSE) can result from several conditions, of which the most common are autoimmune encephalitis and infectious diseases. 10 , 11 Mitochondrial diseases are listed as rare etiology of NORSE, and the current diagnostic recommendations do not contemplate a systematic screening for mitochondrial defects in adults, 10 , 12 , 13 which is still time and resource consuming outside of specialized centers. Since a normal CSF examination rules out the most common differential diagnoses of NORSE, the application of a rapid genetic test, as further diagnostic step, would have been a posteriori the approach of choice in the index patient. Rapid genetic testing strategies have been successfully applied in the setting of fulminant pediatric disorders, opening a window of opportunity when a potentially treatable disorder is untangled. 14 , 15 In our case, the time pressure because of unsuccessful status treatment and the concern of omitting a potentially effective drug, motivated, in the setting of missing guidelines, a difficult therapeutic choice. It remains speculative whether an earlier diagnosis, by means of rapid genetic testing, could have influenced the course of the disease in our patient. However, it would have prevented complications due to inappropriate application of first-line pharmacologic therapies (valproate in the setting of myoclonic epilepsy).
4.195313
0.489258
sec[1]/p[3]
en
0.999996
PMC10117698
https://doi.org/10.1212/NXG.0000000000200063
[ "norse", "rapid", "genetic", "setting", "status", "which", "common", "diseases", "mitochondrial", "time" ]
[ { "code": "6A80.5", "title": "Rapid cycling" }, { "code": "MC81.0", "title": "Tachycardia, unspecified" }, { "code": "QA00.Y", "title": "Other specified general examination or investigation of persons without complaint or reported diagnosis" }, { "code": "7B01.0", "title": "REM sleep behaviour disorder" }, { "code": "BC81.3Z", "title": "Atrial fibrillation, unspecified" }, { "code": "LD27.6Z", "title": "Genetic lipodystrophy, unspecified" }, { "code": "8E02.Z", "title": "Creutzfeldt-Jakob disease, unspecified" }, { "code": "EC20", "title": "Genetic disorders of keratinisation" }, { "code": "AB56", "title": "Hereditary hearing loss" }, { "code": "EC10", "title": "Genetic syndromes with poikiloderma" } ]
=== ICD-11 CODES FOUND === [6A80.5] Rapid cycling Definition: In the context of bipolar type I or bipolar type II disorder, there has been a high frequency of mood episodes (at least four) over the past 12 months. There may be a switch from one polarity of mood to the other, or the mood episodes may be demarcated by a period of remission. In individuals with a high frequency of mood episodes, some may have a shorter duration than those usually observed in bipolar type I or bipolar type II disorder. In particular, depressive periods may only last several da Also known as: Rapid cycling [MC81.0] Tachycardia, unspecified Also known as: Tachycardia, unspecified | heart rate fast | rapid heart | Rapid heart beat | increased heart rate [QA00.Y] Other specified general examination or investigation of persons without complaint or reported diagnosis Also known as: Other specified general examination or investigation of persons without complaint or reported diagnosis | Examination for period of rapid growth in childhood | evaluation of period of rapid growth in childhood | observation of development state of period of rapid growth in childhood | Examination for adolescent development state [7B01.0] REM sleep behaviour disorder Definition: REM sleep behaviour disorder is characterised by repeated episodes of sleep related vocalization or complex motor behaviours that are either documented by polysomnography to occur during REM (rapid eye movement) sleep or are presumed to occur during REM sleep due to a clinical history of dream enactment. Polysomnographic recording (when performed) demonstrates REM sleep without atonia. The disorder may occur as an isolated, idiopathic form but is frequently associated with latent or manifest dis Also known as: REM sleep behaviour disorder | REM - [rapid eye movement] behaviour disorder [BC81.3Z] Atrial fibrillation, unspecified Also known as: Atrial fibrillation, unspecified | Atrial fibrillation | AF - [atrial fibrillation] | rapid atrial fibrillation | A Fib - [atrial fibrillation] [LD27.6Z] Genetic lipodystrophy, unspecified Also known as: Genetic lipodystrophy, unspecified | Genetic lipodystrophy | Hereditary lipodystrophy | Lipodystrophy due to peptidic growth factors deficiency | Hoepffner-Dreyer-Reimers syndrome [8E02.Z] Creutzfeldt-Jakob disease, unspecified Also known as: Creutzfeldt-Jakob disease, unspecified | Genetic prion diseases [EC20] Genetic disorders of keratinisation Definition: Heritable disorders characterised by abnormal epidermal keratinization. They include the ichthyoses and palmoplantar keratodermas. Also known as: Genetic disorders of keratinisation [AB56] Hereditary hearing loss Also known as: Hereditary hearing loss | genetic hearing loss | hereditary deafness Excludes: Congenital hearing impairment | Acquired hearing impairment [EC10] Genetic syndromes with poikiloderma Definition: Hereditary syndromes in which poikiloderma (cutaneous pigmentation, atrophy and telangiectasia) is a conspicuous feature. Also known as: Genetic syndromes with poikiloderma | Poikiloderma with neutropaenia | Poikiloderma with neutropaenia, Clericuzio type | Hereditary sclerosing poikiloderma | Hereditary sclerosing poikiloderma (MIM 173700) === GRAPH WALKS === --- Walk 1 --- [6A80.5] Rapid cycling Def: In the context of bipolar type I or bipolar type II disorder, there has been a high frequency of mood episodes (at least four) over the past 12 months. There may be a switch from one polarity of mood ... --PARENT--> [6A80] Symptomatic and course presentations for mood episodes in mood disorders Def: These categories may be applied to describe the presentation and characteristics of mood episodes in the context of single episode depressive disorder, recurrent depressive disorder, bipolar type I di... --RELATED_TO--> [?] 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 --- [6A80.5] Rapid cycling Def: In the context of bipolar type I or bipolar type II disorder, there has been a high frequency of mood episodes (at least four) over the past 12 months. There may be a switch from one polarity of mood ... --PARENT--> [6A80] Symptomatic and course presentations for mood episodes in mood disorders Def: These categories may be applied to describe the presentation and characteristics of mood episodes in the context of single episode depressive disorder, recurrent depressive disorder, bipolar type I di... --CHILD--> [6A80.1] Panic attacks in mood episodes Def: In the context of a current mood episode (manic, depressive, mixed, or hypomanic), there have been recurrent panic attacks (i.e., at least two) during the past month that occur specifically in respons... --- Walk 3 --- [MC81.0] Tachycardia, unspecified --PARENT--> [MC81] Abnormalities of heart beat Def: Abnormalities of heart beat is arrhythmia which is any disorder of the heart rate or rhythm. It means that the heart beats too quickly, too slowly or with an irregular pattern.... --CHILD--> [MC81.0] Tachycardia, unspecified --- Walk 4 --- [MC81.0] Tachycardia, unspecified --PARENT--> [MC81] Abnormalities of heart beat Def: Abnormalities of heart beat is arrhythmia which is any disorder of the heart rate or rhythm. It means that the heart beats too quickly, too slowly or with an irregular pattern.... --EXCLUDES--> [?] 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.... --- Walk 5 --- [QA00.Y] Other specified general examination or investigation of persons without complaint or reported diagnosis --PARENT--> [QA00] General examination or investigation of persons without complaint or reported diagnosis --PARENT--> [?] Contact with health services for purposes of examination or investigation --- Walk 6 --- [QA00.Y] Other specified general examination or investigation of persons without complaint or reported diagnosis --PARENT--> [QA00] General examination or investigation of persons without complaint or reported diagnosis --CHILD--> [QA00.1] Routine child health examination Def: Routine health check for child over 28 days of age through 19 years of age....
[ "[6A80.5] Rapid cycling\n Def: In the context of bipolar type I or bipolar type II disorder, there has been a high frequency of mood episodes (at least four) over the past 12 months. There may be a switch from one polarity of mood ...\n --PARENT--> [6A80] Symptomatic and course presentations for mood episodes in mood disorders\n Def: These categories may be applied to describe the presentation and characteristics of mood episodes in the context of single episode depressive disorder, recurrent depressive disorder, bipolar type I di...\n --RELATED_TO--> [?] 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, ...", "[6A80.5] Rapid cycling\n Def: In the context of bipolar type I or bipolar type II disorder, there has been a high frequency of mood episodes (at least four) over the past 12 months. There may be a switch from one polarity of mood ...\n --PARENT--> [6A80] Symptomatic and course presentations for mood episodes in mood disorders\n Def: These categories may be applied to describe the presentation and characteristics of mood episodes in the context of single episode depressive disorder, recurrent depressive disorder, bipolar type I di...\n --CHILD--> [6A80.1] Panic attacks in mood episodes\n Def: In the context of a current mood episode (manic, depressive, mixed, or hypomanic), there have been recurrent panic attacks (i.e., at least two) during the past month that occur specifically in respons...", "[MC81.0] Tachycardia, unspecified\n --PARENT--> [MC81] Abnormalities of heart beat\n Def: Abnormalities of heart beat is arrhythmia which is any disorder of the heart rate or rhythm. It means that the heart beats too quickly, too slowly or with an irregular pattern....\n --CHILD--> [MC81.0] Tachycardia, unspecified", "[MC81.0] Tachycardia, unspecified\n --PARENT--> [MC81] Abnormalities of heart beat\n Def: Abnormalities of heart beat is arrhythmia which is any disorder of the heart rate or rhythm. It means that the heart beats too quickly, too slowly or with an irregular pattern....\n --EXCLUDES--> [?] 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....", "[QA00.Y] Other specified general examination or investigation of persons without complaint or reported diagnosis\n --PARENT--> [QA00] General examination or investigation of persons without complaint or reported diagnosis\n --PARENT--> [?] Contact with health services for purposes of examination or investigation", "[QA00.Y] Other specified general examination or investigation of persons without complaint or reported diagnosis\n --PARENT--> [QA00] General examination or investigation of persons without complaint or reported diagnosis\n --CHILD--> [QA00.1] Routine child health examination\n Def: Routine health check for child over 28 days of age through 19 years of age...." ]
6A80.5
Rapid cycling
[ { "from_icd11": "MC81.0", "icd10_code": "R000", "icd10_title": "Tachycardia, unspecified" }, { "from_icd11": "7B01.0", "icd10_code": "G478", "icd10_title": "Other sleep disorders" }, { "from_icd11": "BC81.3Z", "icd10_code": "I4891", "icd10_title": "Unspecified atrial fibrillation" }, { "from_icd11": "LD27.6Z", "icd10_code": "E881", "icd10_title": "Lipodystrophy, not elsewhere classified" }, { "from_icd11": "EC20", "icd10_code": "Q809", "icd10_title": "Congenital ichthyosis, unspecified" }, { "from_icd11": "EC20", "icd10_code": "L998", "icd10_title": "" }, { "from_icd11": "EC20", "icd10_code": "Q80-Q89", "icd10_title": "" }, { "from_icd11": "EC20", "icd10_code": "Q80", "icd10_title": "Congenital ichthyosis" }, { "from_icd11": "EC20", "icd10_code": "Q808", "icd10_title": "Other congenital ichthyosis" }, { "from_icd11": "EC10", "icd10_code": "Q828", "icd10_title": "Other specified congenital malformations of skin" } ]
R000
Tachycardia, unspecified
A 27-year-old female, with underlying T1DM for 17 years, was recently admitted to the hospital in order to achieve better glycemic control. Vital signs at presentation were a temperature of 36.1 °C, a pulse rate of 100 beats/min, a respiratory rate of 28 breaths/min, and blood pressure of 120/85 mm Hg. Past medical history included T1DM managed with an insulin pump 15 years. In recent years, the dosage of insulin was 45 IU/d, and metformin 0.5 g (qid) was added to the therapeutic regimen 3 years ago due to weight gain. On admission, characteristics were noted as follows: her body weight was 75.0 kg; BMI was 28.2 kg/m 2 ; and waist circumference was 105.5 cm. Clinical laboratory analysis found that she was positive for urine ketones, her fasting blood glucose was 10.5 mmol/L, and her glycated hemoglobin (HbA1c) was 7.7%. Her was C-peptide <0.02 ng/mL, insulin antibodies (IAA) were 4.96 RU/mL, islet cell antibodies (ICA) were 6.09 IU/mL, and glutamic acid decarboxylase antibodies (GAD) were 18.44 IU/mL. An abdominal ultrasound indicated that she had a fatty liver. An electrocardiograph (ECG) and auscultation of the lungs showed no significant findings; her liver function, renal function, and thyroid function had no obvious abnormalities. The patient had no smoking and alcohol intake history, but she did have a history of fracture surgery due to a traffic accident and a family history of diabetes.
3.841797
0.983398
sec[1]/p[0]
en
0.999998
37241059
https://doi.org/10.3390/medicina59050827
[ "insulin", "antibodies", "function", "blood", "weight", "that", "liver", "underlying", "recently", "order" ]
[ { "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": "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 === [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 [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 --- [5A44] Insulin-resistance syndromes --PARENT--> [?] Other disorders of glucose regulation or pancreatic internal secretion --CHILD--> [5A41] Hypoglycaemia without associated diabetes --- Walk 2 --- [5A44] Insulin-resistance syndromes --PARENT--> [?] Other disorders of glucose regulation or pancreatic internal secretion --CHILD--> [5A42] Increased secretion of glucagon --- 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 --CHILD--> [5A41] Hypoglycaemia without associated diabetes --- 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--> [QB51.1] Presence of urogenital implants
[ "[5A44] Insulin-resistance syndromes\n --PARENT--> [?] Other disorders of glucose regulation or pancreatic internal secretion\n --CHILD--> [5A41] Hypoglycaemia without associated diabetes", "[5A44] Insulin-resistance syndromes\n --PARENT--> [?] Other disorders of glucose regulation or pancreatic internal secretion\n --CHILD--> [5A42] Increased secretion of glucagon", "[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 --CHILD--> [5A41] Hypoglycaemia without associated diabetes", "[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--> [QB51.1] Presence of urogenital implants" ]
5A44
Insulin-resistance syndromes
[ { "from_icd11": "5A44", "icd10_code": "E10-E14", "icd10_title": "" }, { "from_icd11": "QB51.5", "icd10_code": "Z9641", "icd10_title": "Presence of insulin pump (external) (internal)" }, { "from_icd11": "QB51.5", "icd10_code": "Z964", "icd10_title": "Presence of endocrine implants" }, { "from_icd11": "EF02.0", "icd10_code": "L988", "icd10_title": "Other specified disorders of the skin and subcutaneous tissue" }, { "from_icd11": "EF02.0", "icd10_code": "E881", "icd10_title": "Lipodystrophy, not elsewhere classified" }, { "from_icd11": "PK9C.2", "icd10_code": "T85694A", "icd10_title": "Other mechanical complication of insulin pump, initial encounter" }, { "from_icd11": "PK9C.2", "icd10_code": "T85614A", "icd10_title": "Breakdown (mechanical) of insulin pump, initial encounter" }, { "from_icd11": "PK9C.2", "icd10_code": "T85624A", "icd10_title": "Displacement of insulin pump, initial encounter" }, { "from_icd11": "PK9C.2", "icd10_code": "T85618A", "icd10_title": "Breakdown (mechanical) of other specified internal prosthetic devices, implants and grafts, initial encounter" }, { "from_icd11": "PK9C.2", "icd10_code": "T85628A", "icd10_title": "Displacement of other specified internal prosthetic devices, implants and grafts, initial encounter" }, { "from_icd11": "PK9C.2", "icd10_code": "T85621A", "icd10_title": "Displacement of intraperitoneal dialysis catheter, initial encounter" }, { "from_icd11": "PK9C.2", "icd10_code": "T85611A", "icd10_title": "Breakdown (mechanical) of intraperitoneal dialysis catheter, initial encounter" }, { "from_icd11": "PK9C.2", "icd10_code": "T85698A", "icd10_title": "Other mechanical complication of other specified internal prosthetic devices, implants and grafts, initial encounter" }, { "from_icd11": "PK9C.2", "icd10_code": "T85638A", "icd10_title": "Leakage of other specified internal prosthetic devices, implants and grafts, initial encounter" }, { "from_icd11": "PK9C.2", "icd10_code": "T85610A", "icd10_title": "Breakdown (mechanical) of cranial or spinal infusion catheter, initial encounter" } ]
E10-E14
A 20‐year‐old female patient was referred to our hospital with a 2‐year history of hypertrophic cardiomyopathy (HCM) and one occurrence of syncope. Two years ago, the patient was found to have a cardiac abnormality during an electrocardiograph (ECG) examination with sinus bradycardia and an irregular indoor conduction block. She denied having symptoms of palpitation, chest tightness, or shortness of breath. Echocardiography and CMR suggested HCM with a local narrow heart cavity. The patient was given appropriate HCM medication (details not available) but discontinued this 1 month later without the regular follow‐up. Her parents recalled that approximately 25 days before admission, the patient had sudden syncope with loss of consciousness while walking of 1‐min duration but no symptoms of incontinence, limb twitching, nausea, or vomiting were apparent. The parents recalled the ECG and head CT (Computed Tomography) taken at the time as being normal (results unavailable). The patient was admitted to our hospital and received a comprehensive examination, including somatoscopy (including muscle strength assessment by MRC grade and retinopathy by ophthalmoscope), evaluation of intellectual development by Wechsler Intelligence Scale, physical examination (including Holter, electrocardiogram, echocardiography, cardiac MRI), and laboratory tests (including myocardial enzymes and biochemical indicators).
3.945313
0.98291
sec[1]/sec[1]/p[0]
en
0.999996
37288668
https://doi.org/10.1002/mgg3.2216
[ "including", "syncope", "cardiac", "echocardiography", "parents", "recalled", "referred", "hypertrophic", "cardiomyopathy", "occurrence" ]
[ { "code": "7A24", "title": "Hypersomnia due to a medication or substance" }, { "code": "9D90", "title": "Vision impairment including blindness" }, { "code": "NE61", "title": "Harmful effects of or exposure to noxious substances, chiefly nonmedicinal as to source, not elsewhere classified" }, { "code": "3A50.02", "title": "Haemoglobin H disease (– α/– – included)" }, { "code": "LA8B.Z", "title": "Congenital anomaly of great arteries including arterial duct, unspecified" }, { "code": "MG45.Z", "title": "Syncope or collapse, unspecified" }, { "code": "8D89.0", "title": "Reflex syncope" }, { "code": "MH12.0", "title": "Instantaneous death" }, { "code": "MD12", "title": "Cough" }, { "code": "8D89.1", "title": "Syncope due to autonomic failure" } ]
=== ICD-11 CODES FOUND === [7A24] Hypersomnia due to a medication or substance Definition: Hypersomnia due to a medication or substance is characterised by excessive nocturnal sleep, daytime sleepiness, or excessive napping that is attributable to the sedating effects of medications, alcohol, or other psychoactive substances, including withdrawal syndromes (e.g., from stimulants) and is sufficiently severe to constitute an independent focus of clinical attention. Note: A definitive diagnosis requires use of polysomnography and multiple sleep latency test (MSLT) to rule out other hype Also known as: Hypersomnia due to a medication or substance | Hypersomnia due to substances including medications | Hypersomnolence due to substances including medications Includes: Hypersomnia due to substances including medications [9D90] Vision impairment including blindness Definition: !markdown The table below gives a classification of severity of vision impairment based on visual acuity.  For epidemiological studies, it is recommended to collect the following information on visual acuity for each eye, for both eyes open and for distance and near.  a) Uncorrected visual acuity  b) Presenting visual acuity  c) Best corrected visual acuity  Blindness is also categorized according to the degree of constriction of the central visual field in the better eye to less than 10 Also known as: Vision impairment including blindness [NE61] Harmful effects of or exposure to noxious substances, chiefly nonmedicinal as to source, not elsewhere classified Also known as: Harmful effects of or exposure to noxious substances, chiefly nonmedicinal as to source, not elsewhere classified | Harmful effects of or exposure to noxious substances chiefly nonmedicinal as to source, alcohols | alcohol poisoning | alcohol toxicity | Harmful effects of or exposure to noxious substances chiefly nonmedicinal as to source, Ethanol Excludes: corrosions | Bacterial foodborne intoxications [3A50.02] Haemoglobin H disease (– α/– – included) Definition: Haemoglobin H (HbH) disease is a moderate to severe form of alpha-thalassemia characterised by pronounced microcytic hypochromic haemolytic anaemia. Also known as: Haemoglobin H disease (– α/– – included) | alpha - /- - or mutational forms of alpha-thalassaemia | Alpha thalassaemia intermedia [LA8B.Z] Congenital anomaly of great arteries including arterial duct, unspecified Also known as: Congenital anomaly of great arteries including arterial duct, unspecified | Congenital anomaly of great arteries including arterial duct [MG45.Z] Syncope or collapse, unspecified Also known as: Syncope or collapse, unspecified | Syncope or collapse | Fainting | fainting fit | general collapse [8D89.0] Reflex syncope Definition: Reflex syncope is a transient loss of consciousness with spontaneous recovery and associated with loss of postural tone. Reflex syncope is the most common form of syncope and can occur in individuals with normal autonomic function. The mechanism is believed to be related to blood pooling in the legs followed by reduction in blood return to the heart which triggers a sympathetic tone increase. Vigorous cardiac contractions with an underfilled ventricle are hypothesized to cause reflex loss of sym Also known as: Reflex syncope [MH12.0] Instantaneous death Also known as: Instantaneous death | dropped dead | fatal syncope | instantaneous death unexplained | sudden death Includes: Sudden unexplained death in adult [MD12] Cough Definition: Cough is an important natural defensive mechanism and protective reflex for clearing the upper and lower airways of excessive secretions such as mucus and inhaled particles. Cough is a common symptom of most respiratory disorders and may be indicative of trivial to very serious airway or lung pathology. Also known as: Cough | complaining of cough | coughing | finding of cough | observation of cough Excludes: cough with haemorrhage [8D89.1] Syncope due to autonomic failure Also known as: Syncope due to autonomic failure === GRAPH WALKS === --- Walk 1 --- [7A24] Hypersomnia due to a medication or substance Def: Hypersomnia due to a medication or substance is characterised by excessive nocturnal sleep, daytime sleepiness, or excessive napping that is attributable to the sedating effects of medications, alcoho... --PARENT--> [?] Hypersomnolence disorders Def: Hypersomnolence disorders are characterised by a complaint of daytime sleepiness that is not due to another sleep-wake disorder (e.g. disturbed nocturnal sleep, misaligned circadian rhythm, or breathi... --PARENT--> [07] Sleep-wake disorders Def: Sleep-wake disorders are characterised by difficulty initiating or maintaining sleep (insomnia disorders), excessive sleepiness (hypersomnolence disorders), respiratory disturbance during sleep (sleep... --- Walk 2 --- [7A24] Hypersomnia due to a medication or substance Def: Hypersomnia due to a medication or substance is characterised by excessive nocturnal sleep, daytime sleepiness, or excessive napping that is attributable to the sedating effects of medications, alcoho... --PARENT--> [?] Hypersomnolence disorders Def: Hypersomnolence disorders are characterised by a complaint of daytime sleepiness that is not due to another sleep-wake disorder (e.g. disturbed nocturnal sleep, misaligned circadian rhythm, or breathi... --CHILD--> [7A21] Idiopathic hypersomnia Def: Idiopathic hypersomnia is characterised by daily periods of irrepressible need to sleep or daytime lapses into sleep occurring for at least several months in the absence of cataplexy or hypocretin def... --- Walk 3 --- [9D90] Vision impairment including blindness Def: !markdown The table below gives a classification of severity of vision impairment based on visual acuity.  For epidemiological studies, it is recommended to collect the following information on visual... --CHILD--> [9D90.2] Moderate vision impairment --PARENT--> [9D90] Vision impairment including blindness Def: !markdown The table below gives a classification of severity of vision impairment based on visual acuity.  For epidemiological studies, it is recommended to collect the following information on visual... --- Walk 4 --- [9D90] Vision impairment including blindness Def: !markdown The table below gives a classification of severity of vision impairment based on visual acuity.  For epidemiological studies, it is recommended to collect the following information on visual... --CHILD--> [9D90.2] Moderate vision impairment --PARENT--> [9D90] Vision impairment including blindness Def: !markdown The table below gives a classification of severity of vision impairment based on visual acuity.  For epidemiological studies, it is recommended to collect the following information on visual... --- Walk 5 --- [NE61] Harmful effects of or exposure to noxious substances, chiefly nonmedicinal as to source, not elsewhere classified --EXCLUDES--> [?] Bacterial foodborne intoxications Def: Any condition caused by an intoxication due to a bacterial toxin. Intoxication is by ingestion of contaminated food.... --CHILD--> [?] Botulism Def: A disease caused by an infection with the gram-positive bacteria Clostridium botulinum. This disease commonly presents with abdominal pain, vomiting, acute paralysis, blurred vision, diplopia, and may... --- Walk 6 --- [NE61] Harmful effects of or exposure to noxious substances, chiefly nonmedicinal as to source, not elsewhere classified --EXCLUDES--> [?] Burns Def: A burn is an injury to the tissues caused by a pathological flux of energy which causes cellular destruction and irreversible denaturation of proteins and is primarily caused by thermal or other acute... --EXCLUDES--> [?] Sunburn Def: An injury to the skin causing erythema, tenderness, and sometimes blistering and resulting from excessive exposure to the sun. The reaction is produced by the ultraviolet radiation in sunlight....
[ "[7A24] Hypersomnia due to a medication or substance\n Def: Hypersomnia due to a medication or substance is characterised by excessive nocturnal sleep, daytime sleepiness, or excessive napping that is attributable to the sedating effects of medications, alcoho...\n --PARENT--> [?] Hypersomnolence disorders\n Def: Hypersomnolence disorders are characterised by a complaint of daytime sleepiness that is not due to another sleep-wake disorder (e.g. disturbed nocturnal sleep, misaligned circadian rhythm, or breathi...\n --PARENT--> [07] Sleep-wake disorders\n Def: Sleep-wake disorders are characterised by difficulty initiating or maintaining sleep (insomnia disorders), excessive sleepiness (hypersomnolence disorders), respiratory disturbance during sleep (sleep...", "[7A24] Hypersomnia due to a medication or substance\n Def: Hypersomnia due to a medication or substance is characterised by excessive nocturnal sleep, daytime sleepiness, or excessive napping that is attributable to the sedating effects of medications, alcoho...\n --PARENT--> [?] Hypersomnolence disorders\n Def: Hypersomnolence disorders are characterised by a complaint of daytime sleepiness that is not due to another sleep-wake disorder (e.g. disturbed nocturnal sleep, misaligned circadian rhythm, or breathi...\n --CHILD--> [7A21] Idiopathic hypersomnia\n Def: Idiopathic hypersomnia is characterised by daily periods of irrepressible need to sleep or daytime lapses into sleep occurring for at least several months in the absence of cataplexy or hypocretin def...", "[9D90] Vision impairment including blindness\n Def: !markdown\nThe table below gives a classification of severity of vision impairment based on visual acuity. \nFor epidemiological studies, it is recommended to collect the following information on visual...\n --CHILD--> [9D90.2] Moderate vision impairment\n --PARENT--> [9D90] Vision impairment including blindness\n Def: !markdown\nThe table below gives a classification of severity of vision impairment based on visual acuity. \nFor epidemiological studies, it is recommended to collect the following information on visual...", "[9D90] Vision impairment including blindness\n Def: !markdown\nThe table below gives a classification of severity of vision impairment based on visual acuity. \nFor epidemiological studies, it is recommended to collect the following information on visual...\n --CHILD--> [9D90.2] Moderate vision impairment\n --PARENT--> [9D90] Vision impairment including blindness\n Def: !markdown\nThe table below gives a classification of severity of vision impairment based on visual acuity. \nFor epidemiological studies, it is recommended to collect the following information on visual...", "[NE61] Harmful effects of or exposure to noxious substances, chiefly nonmedicinal as to source, not elsewhere classified\n --EXCLUDES--> [?] Bacterial foodborne intoxications\n Def: Any condition caused by an intoxication due to a bacterial toxin. Intoxication is by ingestion of contaminated food....\n --CHILD--> [?] Botulism\n Def: A disease caused by an infection with the gram-positive bacteria Clostridium botulinum. This disease commonly presents with abdominal pain, vomiting, acute paralysis, blurred vision, diplopia, and may...", "[NE61] Harmful effects of or exposure to noxious substances, chiefly nonmedicinal as to source, not elsewhere classified\n --EXCLUDES--> [?] Burns\n Def: A burn is an injury to the tissues caused by a pathological flux of energy which causes cellular destruction and irreversible denaturation of proteins and is primarily caused by thermal or other acute...\n --EXCLUDES--> [?] Sunburn\n Def: An injury to the skin causing erythema, tenderness, and sometimes blistering and resulting from excessive exposure to the sun. The reaction is produced by the ultraviolet radiation in sunlight...." ]
7A24
Hypersomnia due to a medication or substance
[ { "from_icd11": "7A24", "icd10_code": "G4719", "icd10_title": "Other hypersomnia" }, { "from_icd11": "7A24", "icd10_code": "G4710", "icd10_title": "Hypersomnia, unspecified" }, { "from_icd11": "7A24", "icd10_code": "G4712", "icd10_title": "Idiopathic hypersomnia without long sleep time" }, { "from_icd11": "7A24", "icd10_code": "G4714", "icd10_title": "Hypersomnia due to medical condition" }, { "from_icd11": "7A24", "icd10_code": "G4713", "icd10_title": "Recurrent hypersomnia" }, { "from_icd11": "7A24", "icd10_code": "G471", "icd10_title": "Hypersomnia" }, { "from_icd11": "9D90", "icd10_code": "H5461", "icd10_title": "Unqualified visual loss, right eye, normal vision left eye" }, { "from_icd11": "9D90", "icd10_code": "H5440", "icd10_title": "Blindness, one eye, unspecified eye" }, { "from_icd11": "9D90", "icd10_code": "H5442", "icd10_title": "Blindness, left eye, normal vision right eye" }, { "from_icd11": "9D90", "icd10_code": "H5441", "icd10_title": "Blindness, right eye, normal vision left eye" }, { "from_icd11": "9D90", "icd10_code": "H5462", "icd10_title": "Unqualified visual loss, left eye, normal vision right eye" }, { "from_icd11": "9D90", "icd10_code": "H5442A3", "icd10_title": "Blindness left eye category 3, normal vision right eye" }, { "from_icd11": "9D90", "icd10_code": "H54413A", "icd10_title": "Blindness right eye category 3, normal vision left eye" }, { "from_icd11": "9D90", "icd10_code": "H5442A5", "icd10_title": "Blindness left eye category 5, normal vision right eye" }, { "from_icd11": "9D90", "icd10_code": "H5460", "icd10_title": "Unqualified visual loss, one eye, unspecified" } ]
G4719
Other hypersomnia
Prolonged afebrile neutropenia requiring growth factor support complicated the patient’s initial chemotherapy course and led to a delay in cycle two. A ctDNA level after the first cycle of FOLFOXIRI-Bev decreased to 0.04 MTM/mL . Interval imaging after two cycles of chemotherapy showed a response of all hepatic lesions, with ctDNA level cleared to undetectable (0.00 MTM/mL) . After completing three cycles of chemotherapy, in consultation with surgical oncology, the patient elected to have definitive microwave ablation of the three hepatic metastases. The patient’s bevacizumab was held during the third cycle of chemotherapy, pre-operatively, but was resumed during his fourth cycle, post-ablation. The patient’s ctDNA level remained undetectable (0.00 MTM/mL) throughout the remainder of his adjuvant treatment course. Considering the lack of detectable ctDNA and persistent side effects from chemotherapy experienced by the patient, a shared decision was made to defer the sixth cycle of chemotherapy and, overall, the patient completed five cycles of adjuvant chemotherapy. Colonoscopy one year after surgery was unremarkable, and no new metastatic lesions were noted on repeat CT scan after chemotherapy completion. Of note, the patient’s CEA levels remained within normal limits (≤3.0 ng/mL per institutional assay) throughout his disease course, from diagnosis to recurrence to post-treatment monitoring .
3.923828
0.962891
sec[1]/p[4]
en
0.999997
PMC9795219
https://doi.org/10.3389/fonc.2022.1074786
[ "chemotherapy", "cycle", "ctdna", "course", "cycles", "hepatic", "lesions", "undetectable", "three", "ablation" ]
[ { "code": "QB97", "title": "Contact with health services for chemotherapy session for neoplasm" }, { "code": "QC05.Y", "title": "Other specified prophylactic measures" }, { "code": "QB9Y", "title": "Other specified contact with health services for nonsurgical interventions not involving devices" }, { "code": "3B64.1Y", "title": "Other specified acquired thrombocytopenia" }, { "code": "QC48.Y", "title": "Other specified personal history of medical treatment" }, { "code": "6A80.5", "title": "Rapid cycling" }, { "code": "PA03", "title": "Unintentional land transport traffic event injuring a motor cyclist" }, { "code": "5C50.AZ", "title": "Disorders of urea cycle metabolism, unspecified" }, { "code": "PA23", "title": "Unintentional land transport event unknown whether traffic or nontraffic injuring a motor cyclist" }, { "code": "PA02", "title": "Unintentional land transport traffic event injuring a pedal cyclist" } ]
=== ICD-11 CODES FOUND === [QB97] Contact with health services for chemotherapy session for neoplasm Also known as: Contact with health services for chemotherapy session for neoplasm | antineoplastic chemotherapy regimen | cancer chemotherapy regimen | maintenance chemotherapy for neoplasm | neoplasm chemotherapy [QC05.Y] Other specified prophylactic measures Also known as: Other specified prophylactic measures | Other prophylactic chemotherapy | chemoprophylaxis | prophylactic chemotherapy | Systemic prophylactic chemotherapy [QB9Y] Other specified contact with health services for nonsurgical interventions not involving devices Also known as: Other specified contact with health services for nonsurgical interventions not involving devices | Chemotherapy other than for neoplasm | admission for chemotherapy administration other than for neoplasm | chemotherapy regimen other than for neoplasm | drug therapy other than for neoplasm [3B64.1Y] Other specified acquired thrombocytopenia Also known as: Other specified acquired thrombocytopenia | Acquired thrombocytopenia specified as refractory | Chemotherapy thrombocytopaenia | Liver thrombocytopaenia [QC48.Y] Other specified personal history of medical treatment Also known as: Other specified personal history of medical treatment | Personal history of contraception | history of contraception | Personal history of long-term use of medicaments other than anticoagulants | personal history of long term current use of medicaments [6A80.5] Rapid cycling Definition: In the context of bipolar type I or bipolar type II disorder, there has been a high frequency of mood episodes (at least four) over the past 12 months. There may be a switch from one polarity of mood to the other, or the mood episodes may be demarcated by a period of remission. In individuals with a high frequency of mood episodes, some may have a shorter duration than those usually observed in bipolar type I or bipolar type II disorder. In particular, depressive periods may only last several da Also known as: Rapid cycling [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 [5C50.AZ] Disorders of urea cycle metabolism, unspecified Also known as: Disorders of urea cycle metabolism, unspecified | Disorders of urea cycle metabolism | disorder of urea cycle | disorders of metabolism of ornithine, citrulline, argininosuccinic acid, arginine and ammonia | ammonia metabolic disorder [PA23] Unintentional land transport event unknown whether traffic or nontraffic injuring a motor cyclist Also known as: Unintentional land transport event unknown whether traffic or nontraffic injuring a motor cyclist | unintentional off-road crash injuring a motor cyclist, unknown whether on road | motor bike crash NOS | motor cycle crash NOS | Motorcycle rider injured in collision with railway train or railway vehicle [PA02] Unintentional land transport traffic event injuring a pedal cyclist Also known as: Unintentional land transport traffic event injuring a pedal cyclist | Pedal cyclist injured in collision with pedestrian or animal | Pedal cyclist injured in collision with pedestrian or animal, person injured while boarding or alighting | Pedal cyclist injured in collision with pedestrian or animal, driver injured in traffic accident | Pedal cyclist injured in collision with pedestrian or animal, passenger injured in traffic accident === GRAPH WALKS === --- Walk 1 --- [QB97] Contact with health services for chemotherapy session for neoplasm --PARENT--> [?] Contact with health services for nonsurgical interventions not involving devices --CHILD--> [QB92] Contact with health services for issue of repeat prescription --- Walk 2 --- [QB97] Contact with health services for chemotherapy session for neoplasm --PARENT--> [?] Contact with health services for nonsurgical interventions not involving devices --PARENT--> [?] Reasons for contact with the health services --- Walk 3 --- [QC05.Y] Other specified prophylactic measures --PARENT--> [QC05] Need for certain specified other prophylactic measures --EXCLUDES--> [?] Contact with health services for prophylactic surgery --- Walk 4 --- [QC05.Y] Other specified prophylactic measures --PARENT--> [QC05] Need for certain specified other prophylactic measures --CHILD--> [QC05.0] Isolation Def: Isolation is the 'separation, for the period of communicability, of infected persons from others in such places and under such conditions as to prevent or limit the direct or indirect transmission of ... --- Walk 5 --- [QB9Y] Other specified contact with health services for nonsurgical interventions not involving devices --PARENT--> [?] Contact with health services for nonsurgical interventions not involving devices --CHILD--> [QB92] Contact with health services for issue of repeat prescription --- Walk 6 --- [QB9Y] Other specified contact with health services for nonsurgical interventions not involving devices --PARENT--> [?] Contact with health services for nonsurgical interventions not involving devices --PARENT--> [?] Reasons for contact with the health services
[ "[QB97] Contact with health services for chemotherapy session for neoplasm\n --PARENT--> [?] Contact with health services for nonsurgical interventions not involving devices\n --CHILD--> [QB92] Contact with health services for issue of repeat prescription", "[QB97] Contact with health services for chemotherapy session for neoplasm\n --PARENT--> [?] Contact with health services for nonsurgical interventions not involving devices\n --PARENT--> [?] Reasons for contact with the health services", "[QC05.Y] Other specified prophylactic measures\n --PARENT--> [QC05] Need for certain specified other prophylactic measures\n --EXCLUDES--> [?] Contact with health services for prophylactic surgery", "[QC05.Y] Other specified prophylactic measures\n --PARENT--> [QC05] Need for certain specified other prophylactic measures\n --CHILD--> [QC05.0] Isolation\n Def: Isolation is the 'separation, for the period of communicability, of infected persons from others in such places and under such conditions as to prevent or limit the direct or indirect transmission of ...", "[QB9Y] Other specified contact with health services for nonsurgical interventions not involving devices\n --PARENT--> [?] Contact with health services for nonsurgical interventions not involving devices\n --CHILD--> [QB92] Contact with health services for issue of repeat prescription", "[QB9Y] Other specified contact with health services for nonsurgical interventions not involving devices\n --PARENT--> [?] Contact with health services for nonsurgical interventions not involving devices\n --PARENT--> [?] Reasons for contact with the health services" ]
QB97
Contact with health services for chemotherapy session for neoplasm
[ { "from_icd11": "QB97", "icd10_code": "Z5111", "icd10_title": "Encounter for antineoplastic chemotherapy" }, { "from_icd11": "QB97", "icd10_code": "Z5112", "icd10_title": "Encounter for antineoplastic immunotherapy" }, { "from_icd11": "QB97", "icd10_code": "Z511", "icd10_title": "Encounter for antineoplastic chemotherapy and immunotherapy" }, { "from_icd11": "QB97", "icd10_code": "Z51", "icd10_title": "Encounter for other aftercare and medical care" }, { "from_icd11": "QB9Y", "icd10_code": "Z5181", "icd10_title": "Encounter for therapeutic drug level monitoring" }, { "from_icd11": "QC48.Y", "icd10_code": "Z794", "icd10_title": "Long term (current) use of insulin" }, { "from_icd11": "QC48.Y", "icd10_code": "Z7902", "icd10_title": "Long term (current) use of antithrombotics/antiplatelets" }, { "from_icd11": "QC48.Y", "icd10_code": "Z7982", "icd10_title": "Long term (current) use of aspirin" }, { "from_icd11": "QC48.Y", "icd10_code": "Z7984", "icd10_title": "Long term (current) use of oral hypoglycemic drugs" }, { "from_icd11": "QC48.Y", "icd10_code": "Z79899", "icd10_title": "Other long term (current) drug therapy" }, { "from_icd11": "PA03", "icd10_code": "V299XXD", "icd10_title": "Motorcycle rider (driver) (passenger) injured in unspecified traffic accident, subsequent encounter" }, { "from_icd11": "PA03", "icd10_code": "V234XXA", "icd10_title": "Motorcycle driver injured in collision with car, pick-up truck or van in traffic accident, initial encounter" }, { "from_icd11": "PA03", "icd10_code": "V299XXA", "icd10_title": "Motorcycle rider (driver) (passenger) injured in unspecified traffic accident, initial encounter" }, { "from_icd11": "PA03", "icd10_code": "V2940XA", "icd10_title": "Motorcycle driver injured in collision with unspecified motor vehicles in traffic accident, initial encounter" }, { "from_icd11": "PA03", "icd10_code": "V239XXD", "icd10_title": "Unspecified motorcycle rider injured in collision with car, pick-up truck or van in traffic accident, subsequent encounter" } ]
Z5111
Encounter for antineoplastic chemotherapy
A healthy 12-year-old male with no significant past medical history or drug allergies was playing basketball at his aunt's house when he suddenly developed a severe headache accompanied by nausea and vomiting. He denied any head trauma to his aunt and mother. He was given an over-the-counter analgesic and went to bed, awakening in the early morning hours with another episode of a sudden severe headache that subsided without medication. He went back to bed, but a couple of hours later, his mother noticed that he had wet his bed. When awakened, he was drowsy and confused. His mother took him to the local hospital. He had two tonic-clonic seizure episodes immediately after his arrival and was intubated to protect his airway. A head computed tomographic (CT) scan without contrast showed a ​​6.0 x 3.2 x 3.0 cm right frontal intracerebral hematoma with rupture into the frontal ventricular horn extending into all the ventricles, causing a 1.2 cm shift of the midline . The patient was promptly transferred to our institution for neurosurgical evaluation. The patient arrived at our institution intubated without sedation. The physical examination demonstrated an acutely ill patient unresponsive to painful external stimuli. The head had no evidence of trauma. He did not open his eyes spontaneously or to pain. The pupils were midsize with sluggish pupillary reflexes. He had corneal and gag reflexes present.
3.6875
0.986328
sec[1]/p[0]
en
0.999997
PMC9814825
https://doi.org/10.7759/cureus.32251
[ "head", "mother", "without", "aunt", "headache", "trauma", "went", "hours", "that", "intubated" ]
[ { "code": "NA63", "title": "Traumatic amputation at neck level" }, { "code": "MB4D", "title": "Headache, not elsewhere classified" }, { "code": "ME61", "title": "Subcutaneous swelling, mass or lump of uncertain or unspecified nature" }, { "code": "MB48.3", "title": "Light-headedness" }, { "code": "FB3Z", "title": "Disorders of muscles, unspecified" }, { "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 === [NA63] Traumatic amputation at neck level Also known as: Traumatic amputation at neck level | complete head avulsion | Decapitation | decapitation of head at neck level | severed head Includes: Decapitation [MB4D] Headache, not elsewhere classified Definition: Headache with characteristic features suggesting that it is a unique diagnostic entity, a finding or complaint, but not fulfilling criteria for any of the headache disorders described above. Also known as: Headache, not elsewhere classified | cephalalgia | cephalgia | cephalodynia | pain in head NOS Excludes: Trigeminal neuralgia | Atypical facial pain | Acute headache, not elsewhere classified [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 [MB48.3] Light-headedness Also known as: Light-headedness | light headed [FB3Z] Disorders of muscles, unspecified Also known as: Disorders of muscles, unspecified | disorder of muscle, unspecified | muscle disease | muscular disease | muscular disorder [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 --- [NA63] Traumatic amputation at neck level --PARENT--> [?] Injuries to the neck --CHILD--> [NA21] Open wound of neck --- Walk 2 --- [NA63] Traumatic amputation at neck level --PARENT--> [?] Injuries to the neck --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 3 --- [MB4D] 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.... --PARENT--> [?] Symptoms or signs involving the nervous system --RELATED_TO--> [?] Symptom or complaint of a body part --- Walk 4 --- [MB4D] 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.... --EXCLUDES--> [?] Acute headache, not elsewhere classified --PARENT--> [?] 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.... --- Walk 5 --- [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.... --PARENT--> [?] Symptoms or signs of blood, blood-forming organs, or the immune system --- Walk 6 --- [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.... --PARENT--> [?] General symptoms
[ "[NA63] Traumatic amputation at neck level\n --PARENT--> [?] Injuries to the neck\n --CHILD--> [NA21] Open wound of neck", "[NA63] Traumatic amputation at neck level\n --PARENT--> [?] Injuries to the neck\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...", "[MB4D] 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....\n --PARENT--> [?] Symptoms or signs involving the nervous system\n --RELATED_TO--> [?] Symptom or complaint of a body part", "[MB4D] 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....\n --EXCLUDES--> [?] Acute headache, not elsewhere classified\n --PARENT--> [?] 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....", "[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 --PARENT--> [?] Symptoms or signs of blood, blood-forming organs, or the immune 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--> [?] Enlarged lymph nodes\n Def: Enlarged lymph node is called lymphadenopathy which means the abnormal enlargement of lymph nodes....\n --PARENT--> [?] General symptoms" ]
NA63
Traumatic amputation at neck level
[ { "from_icd11": "NA63", "icd10_code": "S18", "icd10_title": "" }, { "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" }, { "from_icd11": "ME61", "icd10_code": "R221", "icd10_title": "Localized swelling, mass and lump, neck" }, { "from_icd11": "ME61", "icd10_code": "R222", "icd10_title": "Localized swelling, mass and lump, trunk" }, { "from_icd11": "ME61", "icd10_code": "R229", "icd10_title": "Localized swelling, mass and lump, unspecified" }, { "from_icd11": "ME61", "icd10_code": "R20-R23", "icd10_title": "" }, { "from_icd11": "ME61", "icd10_code": "R22", "icd10_title": "Localized swelling, mass and lump of skin and subcutaneous tissue" } ]
S18
The case is of a 29-year-old female of African descent from Haiti who was referred to hematology for severe neutropenia. Notably, she had a history of cardiovascular malformation (ventricular septal defect) surgically repaired at the age of 5 and recurrent skin and oto-sinopulmonary infections (sinusitis, otitis media, and pneumonia) since childhood resulting in progressive hearing loss and chronic bronchiectasis. She also reported anosmia and recurrent blisters of the philtrum, likely herpetic lesions, although no such lesions were present at the time of our examination. Of note, her HSV-1 antibodies were positive on serology. The patient reported no history of tobacco smoking, alcohol use, or substance abuse. Her family history was notable for a brother with recurrent infections but no formal diagnosis of primary immunodeficiency. There was no other known family history of hematologic disorders, immunodeficiency, or malignancy. Family members had been offered genetic testing but to date, no specimens have been sent in for evaluation. Six years prior to her current presentation, she underwent a bone marrow biopsy to evaluate incidentally-discovered neutropenia. The biopsy showed a largely normal marrow with trilineage hematopoiesis, erythroid hypoplasia, and plasmacytosis without light chain restriction. An aspirate could not be performed, and no cytogenetic or molecular testing was available.
3.931641
0.983887
sec[1]/p[0]
en
0.999997
PMC9925260
https://doi.org/10.1155/2023/3888680
[ "recurrent", "family", "neutropenia", "infections", "lesions", "immunodeficiency", "testing", "marrow", "biopsy", "african" ]
[ { "code": "9A78.8", "title": "Recurrent erosion of cornea" }, { "code": "7A22", "title": "Kleine-Levin syndrome" }, { "code": "DC50.1Y", "title": "Other specified secondary peritonitis" }, { "code": "GA33", "title": "Recurrent pregnancy loss" }, { "code": "8C74.1Z", "title": "Periodic paralysis, unspecified" }, { "code": "QE70.Z", "title": "Problems related to primary support group, including family circumstances, unspecified" }, { "code": "2B90.Y", "title": "Other specified malignant neoplasms of colon" }, { "code": "EE61", "title": "Superficial fibromatoses" }, { "code": "9B70", "title": "Inherited retinal dystrophies" }, { "code": "4B00.0Z", "title": "Neutropaenia, unspecified" } ]
=== ICD-11 CODES FOUND === [9A78.8] Recurrent erosion of cornea Also known as: Recurrent erosion of cornea | corneal erosion | non-traumatic recurrent erosion of cornea | recurrent corneal erosion | recurrent erosion syndrome [7A22] Kleine-Levin syndrome Definition: Kleine-Levin syndrome is characterised by recurrent episodes of severe sleepiness in association with cognitive, psychiatric, and behavioural disturbances. A typical episode lasts a median of 10 days (range 2.5–80 days), with rare episodes lasting several weeks to months. During episodes, patients may sleep as long as 16 to 20 hours per day, waking or getting up only to eat and void. When awake during episodes, most patients are exhausted, apathetic, confused, and slow in speaking and answering. Also known as: Kleine-Levin syndrome | recurrent hypersomnolence | hypersomnia-bulimia syndrome Includes: recurrent hypersomnolence [DC50.1Y] Other specified secondary peritonitis Also known as: Other specified secondary peritonitis | Escherichia coli peritonitis | E coli peritonitis | Enterococcal peritonitis | Gram negative peritonitis, not elsewhere classified [GA33] Recurrent pregnancy loss Also known as: Recurrent pregnancy loss | recurrent aborter | recurrent miscarriage | Habitual aborter | habitual or recurrent aborter without current pregnancy Excludes: currently pregnant | with current abortion [8C74.1Z] Periodic paralysis, unspecified Also known as: Periodic paralysis, unspecified | Periodic paralysis | Westphal disease | periodic myotonia | myoplegic dystrophy [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 [2B90.Y] Other specified malignant neoplasms of colon Also known as: Other specified malignant neoplasms of colon | Neuroendocrine neoplasm of colon | Colon endocrine neoplasm | Neuroendocrine carcinoma of colon | NEC - [neuroendocrine carcinoma] of colon [EE61] Superficial fibromatoses Also known as: Superficial fibromatoses | Pachydermodactyly | Camptodactyly or streblodactyly | Familial camptodactyly | Sporadic camptodactyly [9B70] Inherited retinal dystrophies Also known as: Inherited retinal dystrophies | hereditary retinal dystrophies | Amaurosis - hypertrichosis | Autosomal dominant late-onset retinal degeneration | Bothnia retinal dystrophy Includes: Leber congenital amaurosis | Stargardt disease | Vitreoretinal dystrophy [4B00.0Z] Neutropaenia, unspecified Also known as: Neutropaenia, unspecified | Neutropenia | Disorders with decreased neutrophil counts | neutropaenic disorder | neutrophil count below reference range === GRAPH WALKS === --- Walk 1 --- [9A78.8] Recurrent erosion of cornea --PARENT--> [9A78] Certain specified disorders of cornea --CHILD--> [9A78.1] Corneal pigmentations or deposits --- Walk 2 --- [9A78.8] Recurrent erosion of cornea --PARENT--> [9A78] Certain specified disorders of cornea --RELATED_TO--> [?] Injury of conjunctiva or corneal abrasion without mention of foreign body --- Walk 3 --- [7A22] Kleine-Levin syndrome Def: Kleine-Levin syndrome is characterised by recurrent episodes of severe sleepiness in association with cognitive, psychiatric, and behavioural disturbances. A typical episode lasts a median of 10 days ... --PARENT--> [?] Hypersomnolence disorders Def: Hypersomnolence disorders are characterised by a complaint of daytime sleepiness that is not due to another sleep-wake disorder (e.g. disturbed nocturnal sleep, misaligned circadian rhythm, or breathi... --PARENT--> [07] Sleep-wake disorders Def: Sleep-wake disorders are characterised by difficulty initiating or maintaining sleep (insomnia disorders), excessive sleepiness (hypersomnolence disorders), respiratory disturbance during sleep (sleep... --- Walk 4 --- [7A22] Kleine-Levin syndrome Def: Kleine-Levin syndrome is characterised by recurrent episodes of severe sleepiness in association with cognitive, psychiatric, and behavioural disturbances. A typical episode lasts a median of 10 days ... --PARENT--> [?] Hypersomnolence disorders Def: Hypersomnolence disorders are characterised by a complaint of daytime sleepiness that is not due to another sleep-wake disorder (e.g. disturbed nocturnal sleep, misaligned circadian rhythm, or breathi... --CHILD--> [7A21] Idiopathic hypersomnia Def: Idiopathic hypersomnia is characterised by daily periods of irrepressible need to sleep or daytime lapses into sleep occurring for at least several months in the absence of cataplexy or hypocretin def... --- Walk 5 --- [DC50.1Y] Other specified secondary peritonitis --PARENT--> [DC50.1] Secondary peritonitis Def: Peritonitis with evident source of an infecting agent or due to other diseases.... --CHILD--> [DC50.10] Eosinophilic peritonitis Def: 10% or more eosinophils in peritoneal effluent at presentation, and its causes are often obscure. However, cases have been reported with allergic reactions, exposure to drugs such as vancomycin, funga... --- Walk 6 --- [DC50.1Y] Other specified secondary peritonitis --PARENT--> [DC50.1] Secondary peritonitis Def: Peritonitis with evident source of an infecting agent or due to other diseases.... --EXCLUDES--> [?] Neonatal peritonitis Def: Neonatal peritonitis may be bacterial or chemical in origin. The majority of cases of bacterial peritonitis are due to intestinal perforations, ruptured omphaloceles, or ischemic intestinal necrosis. ...
[ "[9A78.8] Recurrent erosion of cornea\n --PARENT--> [9A78] Certain specified disorders of cornea\n --CHILD--> [9A78.1] Corneal pigmentations or deposits", "[9A78.8] Recurrent erosion of cornea\n --PARENT--> [9A78] Certain specified disorders of cornea\n --RELATED_TO--> [?] Injury of conjunctiva or corneal abrasion without mention of foreign body", "[7A22] Kleine-Levin syndrome\n Def: Kleine-Levin syndrome is characterised by recurrent episodes of severe sleepiness in association with cognitive, psychiatric, and behavioural disturbances. A typical episode lasts a median of 10 days ...\n --PARENT--> [?] Hypersomnolence disorders\n Def: Hypersomnolence disorders are characterised by a complaint of daytime sleepiness that is not due to another sleep-wake disorder (e.g. disturbed nocturnal sleep, misaligned circadian rhythm, or breathi...\n --PARENT--> [07] Sleep-wake disorders\n Def: Sleep-wake disorders are characterised by difficulty initiating or maintaining sleep (insomnia disorders), excessive sleepiness (hypersomnolence disorders), respiratory disturbance during sleep (sleep...", "[7A22] Kleine-Levin syndrome\n Def: Kleine-Levin syndrome is characterised by recurrent episodes of severe sleepiness in association with cognitive, psychiatric, and behavioural disturbances. A typical episode lasts a median of 10 days ...\n --PARENT--> [?] Hypersomnolence disorders\n Def: Hypersomnolence disorders are characterised by a complaint of daytime sleepiness that is not due to another sleep-wake disorder (e.g. disturbed nocturnal sleep, misaligned circadian rhythm, or breathi...\n --CHILD--> [7A21] Idiopathic hypersomnia\n Def: Idiopathic hypersomnia is characterised by daily periods of irrepressible need to sleep or daytime lapses into sleep occurring for at least several months in the absence of cataplexy or hypocretin def...", "[DC50.1Y] Other specified secondary peritonitis\n --PARENT--> [DC50.1] Secondary peritonitis\n Def: Peritonitis with evident source of an infecting agent or due to other diseases....\n --CHILD--> [DC50.10] Eosinophilic peritonitis\n Def: 10% or more eosinophils in peritoneal effluent at presentation, and its causes are often obscure. However, cases have been reported with allergic reactions, exposure to drugs such as vancomycin, funga...", "[DC50.1Y] Other specified secondary peritonitis\n --PARENT--> [DC50.1] Secondary peritonitis\n Def: Peritonitis with evident source of an infecting agent or due to other diseases....\n --EXCLUDES--> [?] Neonatal peritonitis\n Def: Neonatal peritonitis may be bacterial or chemical in origin. The majority of cases of bacterial peritonitis are due to intestinal perforations, ruptured omphaloceles, or ischemic intestinal necrosis. ..." ]
9A78.8
Recurrent erosion of cornea
[ { "from_icd11": "7A22", "icd10_code": "G478", "icd10_title": "Other sleep disorders" }, { "from_icd11": "GA33", "icd10_code": "N96", "icd10_title": "Recurrent pregnancy loss" }, { "from_icd11": "8C74.1Z", "icd10_code": "G723", "icd10_title": "Periodic paralysis" }, { "from_icd11": "QE70.Z", "icd10_code": "Z6379", "icd10_title": "Other stressful life events affecting family and household" }, { "from_icd11": "QE70.Z", "icd10_code": "Z6372", "icd10_title": "Alcoholism and drug addiction in family" }, { "from_icd11": "QE70.Z", "icd10_code": "Z638", "icd10_title": "Other specified problems related to primary support group" }, { "from_icd11": "QE70.Z", "icd10_code": "Z639", "icd10_title": "Problem related to primary support group, unspecified" }, { "from_icd11": "QE70.Z", "icd10_code": "Z637", "icd10_title": "Other stressful life events affecting family and household" }, { "from_icd11": "EE61", "icd10_code": "F54", "icd10_title": "Psychological and behavioral factors associated with disorders or diseases classified elsewhere" }, { "from_icd11": "9B70", "icd10_code": "H3552", "icd10_title": "Pigmentary retinal dystrophy" }, { "from_icd11": "9B70", "icd10_code": "H3550", "icd10_title": "Unspecified hereditary retinal dystrophy" }, { "from_icd11": "9B70", "icd10_code": "H3553", "icd10_title": "Other dystrophies primarily involving the sensory retina" }, { "from_icd11": "9B70", "icd10_code": "H3554", "icd10_title": "Dystrophies primarily involving the retinal pigment epithelium" }, { "from_icd11": "9B70", "icd10_code": "H355", "icd10_title": "Hereditary retinal dystrophy" } ]
G478
Other sleep disorders
A 26-year-old gravida 2 para 0, was referred to Princess Christian Maternity Hospital, Freetown, Sierra Leone, with amenorrhea of three months duration a three day history of worsening pelvic pain. She had a prior history of right salpingectomy performed 3 years before presentation as a result of ruptured right tubal EP. On examination, there was moderate tachycardia and lower abdominal tenderness; the pregnancy test was positive, and the transabdominal ultrasound scan revealed a 12-weeks left adnexal EP with a vital fetus and no free fluid collection in the pouch of Douglas . In this public academic hospital No other hematological diagnostic or imaging investigations were available, and they were not included in the free healthcare guaranteed by the national program. Blood tests and magnetic resonance imaging are carried out in other private institutions. A rapid test for hemoglobin was performed and the result was within the normal range. In the presence of the husband, the patient was offered detailed counselling for the management of her condition. Considering the vital fetus, the global consensus indicates the surgical removal of the pregnancy. As a symptom, pain could indicate impending or initial tubal rupture, and the consequent bleeding potentially threatens the patient’s survival. Therefore, emergency exploratory laparotomy was proposed for suspicion of the imminent rupture of the EP.
3.816406
0.983398
sec[2]/p[0]
en
0.999998
37685709
https://doi.org/10.3390/jcm12175642
[ "three", "pain", "tubal", "pregnancy", "vital", "fetus", "free", "imaging", "rupture", "gravida" ]
[ { "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" }, { "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 === [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 [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 --- [1D45] Sandfly fever --PARENT--> [?] Certain arthropod-borne viral fevers --CHILD--> [1D42] O'nyong-nyong fever --- Walk 2 --- [1D45] Sandfly fever --PARENT--> [?] Certain arthropod-borne viral fevers --RELATED_TO--> [?] Central European tick-borne encephalitis --- Walk 3 --- [PA09] Unintentional land transport traffic event injuring an occupant of a low powered passenger vehicle --PARENT--> [?] Unintentional land transport road traffic injury event --CHILD--> [PA00] Unintentional land transport traffic event injuring a pedestrian --- Walk 4 --- [PA09] Unintentional land transport traffic event injuring an occupant of a low powered passenger vehicle --PARENT--> [?] Unintentional land transport road traffic injury event --CHILD--> [PA00] Unintentional land transport traffic event injuring a pedestrian --- Walk 5 --- [LD50.Y] Other specified number anomalies of chromosome X --PARENT--> [LD50] Number anomalies of chromosome X --CHILD--> [LD50.2] Mosaicism, lines with various numbers of X chromosomes Def: A disease caused by embryonic fusion or gain or loss of X chromosomes early in embryonic development, resulting in a subset of cells in the body having an abnormal number of X chromosomes. This diseas... --- Walk 6 --- [LD50.Y] Other specified number anomalies of chromosome X --PARENT--> [LD50] Number anomalies of chromosome X --CHILD--> [LD50.0] Turner syndrome Def: Karyotype missing one X chromosome (45,X0 or 45,X0/46,XX mosaicism); gonads: ovaries (streak); phenotype female with short stature, amenorrhea (hypergonadotropic hypogonadism), absence of sexual devel...
[ "[1D45] Sandfly fever\n --PARENT--> [?] Certain arthropod-borne viral fevers\n --CHILD--> [1D42] O'nyong-nyong fever", "[1D45] Sandfly fever\n --PARENT--> [?] Certain arthropod-borne viral fevers\n --RELATED_TO--> [?] Central European tick-borne encephalitis", "[PA09] Unintentional land transport traffic event injuring an occupant of a low powered passenger vehicle\n --PARENT--> [?] Unintentional land transport road traffic injury event\n --CHILD--> [PA00] Unintentional land transport traffic event injuring a pedestrian", "[PA09] Unintentional land transport traffic event injuring an occupant of a low powered passenger vehicle\n --PARENT--> [?] Unintentional land transport road traffic injury event\n --CHILD--> [PA00] Unintentional land transport traffic event injuring a pedestrian", "[LD50.Y] Other specified number anomalies of chromosome X\n --PARENT--> [LD50] Number anomalies of chromosome X\n --CHILD--> [LD50.2] Mosaicism, lines with various numbers of X chromosomes\n Def: A disease caused by embryonic fusion or gain or loss of X chromosomes early in embryonic development, resulting in a subset of cells in the body having an abnormal number of X chromosomes. This diseas...", "[LD50.Y] Other specified number anomalies of chromosome X\n --PARENT--> [LD50] Number anomalies of chromosome X\n --CHILD--> [LD50.0] Turner syndrome\n Def: Karyotype missing one X chromosome (45,X0 or 45,X0/46,XX mosaicism); gonads: ovaries (streak); phenotype female with short stature, amenorrhea (hypergonadotropic hypogonadism), absence of sexual devel..." ]
1D45
Sandfly fever
[ { "from_icd11": "1D45", "icd10_code": "A931", "icd10_title": "Sandfly fever" }, { "from_icd11": "PA09", "icd10_code": "V30-V39", "icd10_title": "" }, { "from_icd11": "PA09", "icd10_code": "V32", "icd10_title": "Occupant of three-wheeled motor vehicle injured in collision with two- or three-wheeled motor vehicle" }, { "from_icd11": "PA09", "icd10_code": "V329", "icd10_title": "Unspecified occupant of three-wheeled motor vehicle injured in collision with two- or three-wheeled motor vehicle in traffic accident" }, { "from_icd11": "PA09", "icd10_code": "V33", "icd10_title": "Occupant of three-wheeled motor vehicle injured in collision with car, pick-up truck or van" }, { "from_icd11": "PA09", "icd10_code": "V334", "icd10_title": "Person boarding or alighting a three-wheeled motor vehicle injured in collision with car, pick-up truck or van" }, { "from_icd11": "PA09", "icd10_code": "V335", "icd10_title": "Driver of three-wheeled motor vehicle injured in collision with car, pick-up truck or van in traffic accident" }, { "from_icd11": "PA09", "icd10_code": "V336", "icd10_title": "Passenger in three-wheeled motor vehicle injured in collision with car, pick-up truck or van in traffic accident" }, { "from_icd11": "PA09", "icd10_code": "V337", "icd10_title": "Person on outside of three-wheeled motor vehicle injured in collision with car, pick-up truck or van in traffic accident" }, { "from_icd11": "PA09", "icd10_code": "V339", "icd10_title": "Unspecified occupant of three-wheeled motor vehicle injured in collision with car, pick-up truck or van in traffic accident" }, { "from_icd11": "PA09", "icd10_code": "V34", "icd10_title": "Occupant of three-wheeled motor vehicle injured in collision with heavy transport vehicle or bus" }, { "from_icd11": "PA09", "icd10_code": "V349", "icd10_title": "Unspecified occupant of three-wheeled motor vehicle injured in collision with heavy transport vehicle or bus in traffic accident" }, { "from_icd11": "PA09", "icd10_code": "V36", "icd10_title": "Occupant of three-wheeled motor vehicle injured in collision with other nonmotor vehicle" }, { "from_icd11": "PA09", "icd10_code": "V369", "icd10_title": "Unspecified occupant of three-wheeled motor vehicle injured in collision with other nonmotor vehicle in traffic accident" }, { "from_icd11": "PA09", "icd10_code": "V38", "icd10_title": "Occupant of three-wheeled motor vehicle injured in noncollision transport accident" } ]
A931
Sandfly fever
A 77-year-old female patient experienced chronic cough and progressing dyspnea two months before the admission. Initial chest computed tomography (CT) showed no specific findings of infectious pneumonia, or interstitial pneumonia . Flowingly, transthoracic echocardiography exhibited right ventricular enlargement and significant PH (TRPG of 80 mmg). However, computed tomographic pulmonary angiography (CTPA) showed no specific findings of pulmonary embolism, instead of increased diffusive nodules and thickening interlobular septal . Accordingly, the blood coagulation tests showed a slightly hypercoagulative state (D-dimer of 19.38 μg/mL, and fibrin degradation products of 42.20 μg/mL). NT-proBNP level was also elevated . Additionally, no evidence of autoimmune disease was found. Fig. 1 Chest radiography and electrocardiography. A-C CT showed increased diffusive nodules and thickening interlobular septal. D CTPA showed no specific findings of pulmonary embolism. E Impaired of pulmonary perfusion detected by dual-energy CT. F PET-CT showed increased FDG uptake in the abdominal cavity near left pararenal with maximum SUV of 4.26, and the maximum cross-sectional area was about 28 × 18 mm. G TTE revealed enlargement of right ventricle, and compressed D-shaped left ventricle. H Echocardiography showed no evidence of D-shaped left ventricle after treatment. I Indicating improved chest CT after treatment
3.980469
0.976563
sec[1]/p[0]
en
0.999996
PMC10041787
https://doi.org/10.1186/s12959-023-00477-4
[ "pulmonary", "chest", "specific", "ventricle", "computed", "pneumonia", "echocardiography", "enlargement", "ctpa", "embolism" ]
[ { "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": "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" } ]
=== 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 [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 === GRAPH WALKS === --- Walk 1 --- [CB40.Y] Other specified diseases of the respiratory system --PARENT--> [CB40] Certain diseases of the respiratory system --CHILD--> [CB40.2] Pulmonary collapse --- Walk 2 --- [CB40.Y] Other specified diseases of the respiratory system --PARENT--> [CB40] Certain diseases of the respiratory system --CHILD--> [CB40.0] Ciliary dyskinesia Def: Defective function of the cilia lining the respiratory tract (lower and upper, sinuses, Eustachian tube, middle ear) resulting in altered mucociliary transport and manifesting as recurrent upper and l... --- 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--> [LA75.0] Accessory lobe of lung Def: An extra lobe of lung beyond the 3 on the right and the 2 on the left... --- Walk 5 --- [CA40.Z] Pneumonia, organism unspecified --PARENT--> [CA40] Pneumonia Def: A disease of the lungs, frequently but not always caused by an infection with bacteria, virus, fungus, or parasite. This disease is characterised by fever, chills, cough with sputum production, chest ... --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.... --- Walk 6 --- [CA40.Z] Pneumonia, organism unspecified --PARENT--> [CA40] Pneumonia Def: A disease of the lungs, frequently but not always caused by an infection with bacteria, virus, fungus, or parasite. This disease is characterised by fever, chills, cough with sputum production, chest ... --CHILD--> [CA40.2] Fungal pneumonia
[ "[CB40.Y] Other specified diseases of the respiratory system\n --PARENT--> [CB40] Certain diseases of the respiratory system\n --CHILD--> [CB40.2] Pulmonary collapse", "[CB40.Y] Other specified diseases of the respiratory system\n --PARENT--> [CB40] Certain diseases of the respiratory system\n --CHILD--> [CB40.0] Ciliary dyskinesia\n Def: Defective function of the cilia lining the respiratory tract (lower and upper, sinuses, Eustachian tube, middle ear) resulting in altered mucociliary transport and manifesting as recurrent upper and l...", "[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--> [LA75.0] Accessory lobe of lung\n Def: An extra lobe of lung beyond the 3 on the right and the 2 on the left...", "[CA40.Z] Pneumonia, organism unspecified\n --PARENT--> [CA40] Pneumonia\n Def: A disease of the lungs, frequently but not always caused by an infection with bacteria, virus, fungus, or parasite. This disease is characterised by fever, chills, cough with sputum production, chest ...\n --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....", "[CA40.Z] Pneumonia, organism unspecified\n --PARENT--> [CA40] Pneumonia\n Def: A disease of the lungs, frequently but not always caused by an infection with bacteria, virus, fungus, or parasite. This disease is characterised by fever, chills, cough with sputum production, chest ...\n --CHILD--> [CA40.2] Fungal pneumonia" ]
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
We present a case of a 50-year-old male with a longstanding history of ulcerative colitis who got diagnosed with advanced unresectable colon cancer at the hepatic flexure with extension into the peri-colonic fascia in the setting of hematochezia. The patient's medical history was significant for a 50-pound weight loss in the last five months preceding the diagnosis alongside worsening abdominal pain. On imaging, there were concerns for multiple enlarged abdominal lymph nodes as well as the potential involvement of the second and third part of the duodenum by the hepatic flexure carcinoma. The cancer was considered to be unresectable and potentially metastatic; therefore, systemic therapy was recommended. A biopsy of the hepatic flexure mass came back as adenocarcinoma with squamous differentiation. Given his otherwise young age and good performance status, the patient received triplet chemotherapy with targeted therapy (FOLFOXIRI with bevacizumab). He had an excellent clinical and radiographic response allowing for conversion surgery. Final pathology came back as ypT4bN0 (0 out of 30 lymph nodes), with no evidence of metastases and grade 3 tumor regression was noted. However, there were concerns about the margins being positive on the duodenal side as well as tumor deposits noted with the specimen. The patient underwent a subtotal colectomy given his prior history of inflammatory bowel disease.
3.886719
0.981445
sec[1]/p[0]
en
0.999997
PMC10428188
https://doi.org/10.7759/cureus.43391
[ "hepatic", "flexure", "unresectable", "cancer", "abdominal", "concerns", "lymph", "nodes", "well", "came" ]
[ { "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": "EA91.Y", "title": "Other specified lichen planus" }, { "code": "EC23.0", "title": "Non-syndromic genetically-determined hypermelanosis or lentiginosis" }, { "code": "EA90.52", "title": "Flexural and intertriginous psoriasis" }, { "code": "2D85", "title": "Malignant neoplasm metastasis in large intestine" }, { "code": "2B90.0Y&XA95L3", "title": "Malignant neoplasm of hepatic flexure" } ]
=== 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 [EA91.Y] Other specified lichen planus Also known as: Other specified lichen planus | Miscellaneous specified forms of lichen planus | Annular lichen planus | Atrophic lichen planus | Bullous lichen planus [EC23.0] Non-syndromic genetically-determined hypermelanosis or lentiginosis Also known as: Non-syndromic genetically-determined hypermelanosis or lentiginosis | Familial progressive hyperpigmentation | Familial generalised lentiginosis | Inherited patterned lentiginosis | Centrofacial lentiginosis [EA90.52] Flexural and intertriginous psoriasis Definition: Psoriasis involving flexures (retro-auricular folds, axillae, crural folds) and/or intertriginous areas (groins, under the breasts and, in obese individuals, abdominal apron fold). It may occur on its own or in association with seborrhoeic psoriasis or chronic plaque psoriasis. Plaques are thin, shiny and beef-red in colour with minimal scale. They may become secondarily fissured and/or macerated. Also known as: Flexural and intertriginous psoriasis | Flexural psoriasis | Intertriginous psoriasis | Inverse psoriasis | Psoriasis inversa [2D85] Malignant neoplasm metastasis in large intestine Definition: The spread of cancer to the large intestine; this may be from a primary colon or rectal cancer to another location in the large intestine, or from a cancer at a distant site or organ. Also known as: Malignant neoplasm metastasis in large intestine | secondary malignant neoplasm in large intestine | large intestine metastasis | Malignant neoplasm metastasis in colon | colon metastasis Includes: Malignant neoplasm metastasis in colon | Malignant neoplasm metastasis in rectum === GRAPH WALKS === --- Walk 1 --- [DB9Z] Diseases of liver, unspecified --PARENT--> [?] Diseases of liver --RELATED_TO--> [?] Metabolic or transporter liver disease --- Walk 2 --- [DB9Z] Diseases of liver, unspecified --PARENT--> [?] Diseases of liver --RELATED_TO--> [?] 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... --- 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 --CHILD--> [DB97.1] Hepatic berylliosis --- 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--> [?] 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... --- 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--> [?] Metabolic or transporter liver disease", "[DB9Z] Diseases of liver, unspecified\n --PARENT--> [?] Diseases of liver\n --RELATED_TO--> [?] 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...", "[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 --CHILD--> [DB97.1] Hepatic berylliosis", "[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...", "[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
A 5-day-old male neonate was received in the nursery emergency of our hospital in a state of shock. The short history depicted that the neonate was a product of consanguineous marriage and was born in a private hospital through spontaneous vaginal delivery. The neonate had an ulcer over the vertex since birth. The ulcer was being managed with dressings. The neonate was going well when during change of dressing massive hemorrhage started. The medical staff of that hospital tightly packed the wound and referred the patient to our hospital for further management. On examination the patient had severe pallor, cold extremities, and impalpable pulses. Fortunately the blood was arranged in the meanwhile; the patient was transfused and then taken directly to the operation theatre. At operation the defect was identified on the vertex as ACC involving scalp, part of skull bone and meninges. It was found that the ulcer had eroded the superior sagittal sinus thus causing tremendous hemorrhage. The superior sagittal sinus was repaired by the neurosurgeon which resulted in hemostasis. The defect was covered with a transposition flap and donor area was covered with split thickness skin graft . Postoperative recovery was uneventful. The patient was started orally on the same day of the operation. At follow up both the flap and graft were healthy; the thigh wound was also healing. The patient is doing well now.
3.466797
0.989258
sec[1]/p[0]
en
0.999996
26023367
N/A
[ "neonate", "that", "ulcer", "vertex", "well", "hemorrhage", "wound", "defect", "sagittal", "sinus" ]
[ { "code": "5A00.00", "title": "Permanent congenital hypothyroidism with diffuse goitre" }, { "code": "KB45", "title": "Neonatal hypertension" }, { "code": "KB2D", "title": "Respiratory failure of newborn" }, { "code": "KB89.1", "title": "Short bowel syndrome in neonate" }, { "code": "KC5Y", "title": "Other specified postnatal iatrogenic skin injury" }, { "code": "8A80.Z", "title": "Migraine, unspecified" }, { "code": "QA76", "title": "Medication or substance that is known to be an allergen without injury or harm" }, { "code": "PL13.6", "title": "Medication or substance that is known to be an allergen, as mode of injury or harm" }, { "code": "9C40.A0", "title": "Papilloedema" }, { "code": "PA6Z", "title": "Unintentional fall from unspecified height" } ]
=== ICD-11 CODES FOUND === [5A00.00] Permanent congenital hypothyroidism with diffuse goitre Definition: A condition caused by a partial or complete loss of thyroid function due to failure of the thyroid to correctly develop during the antenatal period. This condition is characterised by a swollen, smooth thyroid gland, and in infants by a dull look, puffy face, and thick tongue that sticks out. This condition may also present with choking episodes, constipation, dry brittle hair, jaundice, lack of muscle tone, low hairline, poor feeding, short height, sleepiness, or sluggishness. Also known as: Permanent congenital hypothyroidism with diffuse goitre | congenital hypothyroidism with diffuse goitre | goitrous cretin | congenital diffuse goitre | congenital diffuse struma Excludes: transitory congenital goitre with normal function [KB45] Neonatal hypertension Definition: Hypertension is defined by a systolic blood pressure in a neonate which is >95th percentile for age and sex on 3 separate occasions Also known as: Neonatal hypertension | newborn hypertension | newborn essential hypertension | newborn benign essential hypertension | newborn benign hypertension [KB2D] Respiratory failure of newborn Definition: Acute or chronic respiratory failure in a newborn. Neonates in acute respiratory failure require respiratory support. Also known as: Respiratory failure of newborn | neonatal respiratory failure | inadequate pulmonary ventilation of newborn | newborn lung insufficiency | newborn pulmonary function inadequate [KB89.1] Short bowel syndrome in neonate Definition: Short bowel syndrome in neonate is a condition originating in the perinatal period in which nutrients are not properly absorbed due to either surgical removal of a large portion of the small intestine or rarely due to the complete dysfunction of a large segment of small intestine. Also known as: Short bowel syndrome in neonate | SBS - [short bowel syndrome] in neonate Excludes: Congenital short bowel [KC5Y] Other specified postnatal iatrogenic skin injury Also known as: Other specified postnatal iatrogenic skin injury | Neonatal extravasation injury | Iatrogenic neonatal dystrophic calcification | Heel-prick calcinosis | Neonatal pressure ulcer [8A80.Z] Migraine, unspecified Also known as: Migraine, unspecified | Migraine [QA76] Medication or substance that is known to be an allergen without injury or harm Definition: Medication that has previously been identified as an allergen to the patient is administered, but does not result in injury or harm. Also known as: Medication or substance that is known to be an allergen without injury or harm Excludes: Medication or substance that is known to be an allergen, as mode of injury or harm [PL13.6] Medication or substance that is known to be an allergen, as mode of injury or harm Also known as: Medication or substance that is known to be an allergen, as mode of injury or harm | medication error relating to known allergy to drug or substance | adverse drug event relating to known allergy to drug or substance [9C40.A0] Papilloedema Definition: Optic disc swelling that results from increased intracranial pressure Also known as: Papilloedema | Optic disc swelling that results from increased intracranial pressure Includes: Optic disc swelling that results from increased intracranial pressure [PA6Z] Unintentional fall from unspecified height Also known as: Unintentional fall from unspecified height | fall NOS | accidental fall | fall causing injury that resulted in death | fell NOS === GRAPH WALKS === --- Walk 1 --- [5A00.00] Permanent congenital hypothyroidism with diffuse goitre Def: A condition caused by a partial or complete loss of thyroid function due to failure of the thyroid to correctly develop during the antenatal period. This condition is characterised by a swollen, smoot... --EXCLUDES--> [?] Neonatal goitre, not elsewhere classified Def: A paediatric condition characterised by swelling of the thyroid gland of a newborn with associated swelling of the neck or larynx that is not classified elsewhere.... --PARENT--> [?] Transitory neonatal disorders of thyroid function Def: A group of paediatric conditions in which there is a temporary disorder in a newborn or infant associated with the thyroid.... --- Walk 2 --- [5A00.00] Permanent congenital hypothyroidism with diffuse goitre Def: A condition caused by a partial or complete loss of thyroid function due to failure of the thyroid to correctly develop during the antenatal period. This condition is characterised by a swollen, smoot... --PARENT--> [5A00.0] Congenital hypothyroidism Def: Hypothyroidism is a condition where the thyroid gland produces too little or no thyroid hormone, and the condition arises at birth. Common clinical features include decreased activity and increased sl... --CHILD--> [5A00.01] Permanent congenital hypothyroidism without goitre Def: This is a permanent congenital state in which the thyroid gland does not make enough thyroid hormone. This diagnosis is without swelling of the thyroid gland.... --- Walk 3 --- [KB45] Neonatal hypertension Def: Hypertension is defined by a systolic blood pressure in a neonate which is >95th percentile for age and sex on 3 separate occasions... --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.... --RELATED_TO--> [?] Patent arterial duct Def: A congenital cardiovascular finding in which the arterial duct (ductus arteriosus) is open beyond the normal age of spontaneous closure.... --- Walk 4 --- [KB45] Neonatal hypertension Def: Hypertension is defined by a systolic blood pressure in a neonate which is >95th percentile for age and sex on 3 separate occasions... --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--> [KB40] Neonatal cardiac failure Def: Cardiac failure originating in the neonatal period... --- Walk 5 --- [KB2D] Respiratory failure of newborn Def: Acute or chronic respiratory failure in a newborn. Neonates in acute respiratory failure require respiratory support.... --PARENT--> [?] Respiratory disorders specific to the perinatal or neonatal period Def: A group of conditions occurring during the period of time around childbirth, especially the five months before and one month after birth which are associated with the cardiovascular or respiratory sys... --RELATED_TO--> [?] Primary central sleep apnoea of infancy Def: Primary central sleep apnoea of infancy is characterised by prolonged (> 20 seconds), predominantly central apnoeas or periodic breathing during more than 5% of total sleep time in an infant of at lea... --- Walk 6 --- [KB2D] Respiratory failure of newborn Def: Acute or chronic respiratory failure in a newborn. Neonates in acute respiratory failure require respiratory support.... --PARENT--> [?] Respiratory disorders specific to the perinatal or neonatal period Def: A group of conditions occurring during the period of time around childbirth, especially the five months before and one month after birth which are associated with the cardiovascular or respiratory sys... --RELATED_TO--> [?] Primary central sleep apnoea of infancy Def: Primary central sleep apnoea of infancy is characterised by prolonged (> 20 seconds), predominantly central apnoeas or periodic breathing during more than 5% of total sleep time in an infant of at lea...
[ "[5A00.00] Permanent congenital hypothyroidism with diffuse goitre\n Def: A condition caused by a partial or complete loss of thyroid function due to failure of the thyroid to correctly develop during the antenatal period. This condition is characterised by a swollen, smoot...\n --EXCLUDES--> [?] Neonatal goitre, not elsewhere classified\n Def: A paediatric condition characterised by swelling of the thyroid gland of a newborn with associated swelling of the neck or larynx that is not classified elsewhere....\n --PARENT--> [?] Transitory neonatal disorders of thyroid function\n Def: A group of paediatric conditions in which there is a temporary disorder in a newborn or infant associated with the thyroid....", "[5A00.00] Permanent congenital hypothyroidism with diffuse goitre\n Def: A condition caused by a partial or complete loss of thyroid function due to failure of the thyroid to correctly develop during the antenatal period. This condition is characterised by a swollen, smoot...\n --PARENT--> [5A00.0] Congenital hypothyroidism\n Def: Hypothyroidism is a condition where the thyroid gland produces too little or no thyroid hormone, and the condition arises at birth. Common clinical features include decreased activity and increased sl...\n --CHILD--> [5A00.01] Permanent congenital hypothyroidism without goitre\n Def: This is a permanent congenital state in which the thyroid gland does not make enough thyroid hormone. This diagnosis is without swelling of the thyroid gland....", "[KB45] Neonatal hypertension\n Def: Hypertension is defined by a systolic blood pressure in a neonate which is >95th percentile for age and sex on 3 separate occasions...\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 --RELATED_TO--> [?] Patent arterial duct\n Def: A congenital cardiovascular finding in which the arterial duct (ductus arteriosus) is open beyond the normal age of spontaneous closure....", "[KB45] Neonatal hypertension\n Def: Hypertension is defined by a systolic blood pressure in a neonate which is >95th percentile for age and sex on 3 separate occasions...\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--> [KB40] Neonatal cardiac failure\n Def: Cardiac failure originating in the neonatal period...", "[KB2D] Respiratory failure of newborn\n Def: Acute or chronic respiratory failure in a newborn. Neonates in acute respiratory failure require respiratory support....\n --PARENT--> [?] Respiratory disorders specific to the perinatal or neonatal period\n Def: A group of conditions occurring during the period of time around childbirth, especially the five months before and one month after birth which are associated with the cardiovascular or respiratory sys...\n --RELATED_TO--> [?] Primary central sleep apnoea of infancy\n Def: Primary central sleep apnoea of infancy is characterised by prolonged (> 20 seconds), predominantly central apnoeas or periodic breathing during more than 5% of total sleep time in an infant of at lea...", "[KB2D] Respiratory failure of newborn\n Def: Acute or chronic respiratory failure in a newborn. Neonates in acute respiratory failure require respiratory support....\n --PARENT--> [?] Respiratory disorders specific to the perinatal or neonatal period\n Def: A group of conditions occurring during the period of time around childbirth, especially the five months before and one month after birth which are associated with the cardiovascular or respiratory sys...\n --RELATED_TO--> [?] Primary central sleep apnoea of infancy\n Def: Primary central sleep apnoea of infancy is characterised by prolonged (> 20 seconds), predominantly central apnoeas or periodic breathing during more than 5% of total sleep time in an infant of at lea..." ]
5A00.00
Permanent congenital hypothyroidism with diffuse goitre
[ { "from_icd11": "5A00.00", "icd10_code": "E071", "icd10_title": "Dyshormogenetic goiter" }, { "from_icd11": "5A00.00", "icd10_code": "E030", "icd10_title": "Congenital hypothyroidism with diffuse goiter" }, { "from_icd11": "KB45", "icd10_code": "P292", "icd10_title": "Neonatal hypertension" }, { "from_icd11": "KB2D", "icd10_code": "P285", "icd10_title": "Respiratory failure of newborn" }, { "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" } ]
E071
Dyshormogenetic goiter
We present the case of a 23-year-old female who was diagnosed with GSD type Ia shortly after birth. She was hospitalized for the first time at the age of 6 months for hypoglycaemia and metabolic acidosis that occurred during a respiratory infection. She had a doll-like facial appearance, hepatomegaly and kidney enlargement. She had been repeatedly hospitalized for episodes of enormous hypoglycaemia during infancy and adolescence. The patient was treated out of hospital with frequent meals rich in carbohydrates during the day and every 2–3 h during the night and as a result she developed obesity. Besides nutritional therapy, she was also treated with allopurinol for hyperuricaemia. She came to our clinic at the age of 22 years for the diagnostic evaluation of arterial hypertension and dyslipidaemia. Her weight was initially 80 kg, height was 157 cm and BMI was 32.5. The levels of uric acid were 425 nmol/l, LDL 3 mmol/l, HDL 0.8 mmol/l, cholesterol 5.2 mmol/l and TG 2 mmol/l. Her in-office blood pressure measurement repeatedly showed raised values (160/90 mmHg in average). We carried out a 24-h ambulatory blood pressure monitoring, which revealed normal daily and average 24-h values of both systolic and diastolic pressure, but also the non-dipping pattern of systolic pressure during the night . The latter can be attributed to excessive nocturnal eating and consequently disturbed sleeping pattern.
4.035156
0.97998
sec[1]/p[0]
en
0.999997
24683476
https://doi.org/10.1530/EDM-13-0056
[ "mmol", "pressure", "hospitalized", "hypoglycaemia", "repeatedly", "treated", "night", "blood", "average", "systolic" ]
[ { "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": "EH90.Z", "title": "Pressure ulcer of unspecified grade" }, { "code": "MB23.L", "title": "Pressured speech" }, { "code": "MD30.Z", "title": "Chest pain, unspecified" }, { "code": "CB22.Y", "title": "Other specified diseases of mediastinum, not elsewhere classified" }, { "code": "BA2Z", "title": "Hypotension, unspecified" }, { "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 [EH90.Z] Pressure ulcer of unspecified grade Also known as: Pressure ulcer of unspecified grade | Pressure ulceration | pressure injury | pressure ulcer | decubitus ulcer [MB23.L] Pressured speech Definition: Speech in which the person feels undue pressure to get the words out. The person’s speech is usually rapid, loud, and emphatic and may be difficult or impossible to interrupt. Frequently, the person talks without any social stimulation and may continue to talk even though no one is listening. Also known as: Pressured speech Excludes: Schizophrenia or other primary psychotic disorders | Bipolar or related disorders [MD30.Z] Chest pain, unspecified Also known as: Chest pain, unspecified | Pain in throat or chest | chest pain NOS | pain in chest | chest pressure [CB22.Y] Other specified diseases of mediastinum, not elsewhere classified Also known as: Other specified diseases of mediastinum, not elsewhere classified | Hernia of mediastinum | mediastinal hernia | mediastinal herniation | Infectious mediastinitis [BA2Z] Hypotension, unspecified Also known as: Hypotension, unspecified | hypopiesis | low blood pressure | arterial hypotension NOS | decreased blood pressure [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--> [?] Proteinuria Def: Excessive serum proteins in the urine, such as in renal disease when albumin is the main protein, but also may be due to other proteins such as immunoglobulin light chains in plasma cell dyscrasia suc... --- Walk 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... --PARENT--> [?] Glomerular diseases Def: Any disease characterised by pathological changes to the glomerulus.... --- 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--> [?] 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 4 --- [GB42.0] Albuminuria, Grade A2 Def: Presence of excessive albumin in the urine, indicating abnormal permeability glomerular filtration. Can be quantitated by either timed collections or spot urine samples with the concentration adjusted... --PARENT--> [GB42] Persistent proteinuria or albuminuria Def: Persistent albuminuria >3mg/mmol creatinine or >30mg/day is regarded as abnormal, indicative and often the first manifestation of chronic kidney disease (CKD). In surveillance for CKD in “at risk” pat... --CHILD--> [GB42.0] Albuminuria, Grade A2 Def: Presence of excessive albumin in the urine, indicating abnormal permeability glomerular filtration. Can be quantitated by either timed collections or spot urine samples with the concentration adjusted... --- Walk 5 --- [MA18.0Y] Other specified elevated blood glucose level --PARENT--> [MA18.0] Elevated blood glucose level --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--> [?] 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....
[ "[GB42.1] Albuminuria, Grade A3\n Def: Presence of excessive albumin in the urine, indicating abnormal permeability glomerular filtration. Can be quantitated by either timed collections or spot urine samples with the concentration adjusted...\n --PARENT--> [GB42] Persistent proteinuria or albuminuria\n Def: Persistent albuminuria >3mg/mmol creatinine or >30mg/day is regarded as abnormal, indicative and often the first manifestation of chronic kidney disease (CKD). In surveillance for CKD in “at risk” pat...\n --EXCLUDES--> [?] Proteinuria\n Def: Excessive serum proteins in the urine, such as in renal disease when albumin is the main protein, but also may be due to other proteins such as immunoglobulin light chains in plasma cell dyscrasia suc...", "[GB42.1] 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 --PARENT--> [?] Glomerular diseases\n Def: Any disease characterised by pathological changes to the glomerulus....", "[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--> [?] 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 --CHILD--> [GB42.0] Albuminuria, Grade A2\n Def: Presence of excessive albumin in the urine, indicating abnormal permeability glomerular filtration. Can be quantitated by either timed collections or spot urine samples with the concentration adjusted...", "[MA18.0Y] Other specified elevated blood glucose level\n --PARENT--> [MA18.0] Elevated blood glucose level\n --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--> [?] 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...." ]
GB42.1
Albuminuria, Grade A3
[ { "from_icd11": "EH90.Z", "icd10_code": "L89623", "icd10_title": "Pressure ulcer of left heel, stage 3" }, { "from_icd11": "EH90.Z", "icd10_code": "L89621", "icd10_title": "Pressure ulcer of left heel, stage 1" }, { "from_icd11": "EH90.Z", "icd10_code": "L89899", "icd10_title": "Pressure ulcer of other site, unspecified stage" }, { "from_icd11": "EH90.Z", "icd10_code": "L89620", "icd10_title": "Pressure ulcer of left heel, unstageable" }, { "from_icd11": "EH90.Z", "icd10_code": "L89622", "icd10_title": "Pressure ulcer of left heel, stage 2" }, { "from_icd11": "EH90.Z", "icd10_code": "L89892", "icd10_title": "Pressure ulcer of other site, stage 2" }, { "from_icd11": "EH90.Z", "icd10_code": "L89519", "icd10_title": "Pressure ulcer of right ankle, unspecified stage" }, { "from_icd11": "EH90.Z", "icd10_code": "L89891", "icd10_title": "Pressure ulcer of other site, stage 1" }, { "from_icd11": "EH90.Z", "icd10_code": "L89610", "icd10_title": "Pressure ulcer of right heel, unstageable" }, { "from_icd11": "EH90.Z", "icd10_code": "L89893", "icd10_title": "Pressure ulcer of other site, stage 3" }, { "from_icd11": "EH90.Z", "icd10_code": "L89890", "icd10_title": "Pressure ulcer of other site, unstageable" }, { "from_icd11": "EH90.Z", "icd10_code": "L89629", "icd10_title": "Pressure ulcer of left heel, unspecified stage" }, { "from_icd11": "EH90.Z", "icd10_code": "L89619", "icd10_title": "Pressure ulcer of right heel, unspecified stage" }, { "from_icd11": "EH90.Z", "icd10_code": "L8945", "icd10_title": "Pressure ulcer of contiguous site of back, buttock and hip, unstageable" }, { "from_icd11": "EH90.Z", "icd10_code": "L89894", "icd10_title": "Pressure ulcer of other site, stage 4" } ]
L89623
Pressure ulcer of left heel, stage 3
A 66-year-old male patient with a history of prostatectomy due to prostate carcinoma and with a persistent single osteoblastic osseous metastasis (left os ilium) presented to our department with a first diagnosis of stage III AITL with exclusive lymph node manifestation. After five courses of CHOP, peripheral blood stem cell (PBSC) apheresis between each course of DHAP and DHAC was performed. At the timepoint of HD chemotherapy (BEAM) and ASCT, the patient was in complete remission. Within 6 months upon ASCT, early relapse occurred, and despite two courses of salvage treatment with gemcitabine and oxaliplatin, the disease progressed. The PSMA-PET result confirmed a stable disease (M1 oss.) of prostate carcinoma. Due to AITL progression, treatment was rotated to all-oral TEPIP (q4w, d1-7), and complete and durable remission (24 months) was achieved within two courses . Finally, treatment was terminated due to long-lasting CR after 2 years. Within the following 3 months, the patient relapsed with lymphoma infiltration of the skin, lymph nodes, and bone marrow (stage IV). At the same timepoint, a myelodysplastic neoplasm (MDS-RS-MLD) was incidentally diagnosed. TEPIP was re-initiated in five-weekly courses, resulting in a renewed very good PR within 3 months . Due to MDS-related cytopenia, TEPIP was replaced with 5-azacitidine. However, the patient died due to progression to AML at 5 months later.
3.982422
0.977051
sec[2]/sec[1]/sec[3]/p[0]
en
0.999996
PMC10250661
https://doi.org/10.3389/fonc.2023.1177330
[ "courses", "within", "tepip", "prostate", "carcinoma", "stage", "aitl", "lymph", "five", "timepoint" ]
[ { "code": "LA8Y", "title": "Other specified structural developmental anomaly of heart or great vessels" }, { "code": "8B10.Y", "title": "Other specified transient ischaemic attack" }, { "code": "6A80", "title": "Symptomatic and course presentations for mood episodes in mood disorders" }, { "code": "LA8C.1", "title": "Anomalous aortic origin or course of coronary artery" }, { "code": "8B22.Y", "title": "Other specified cerebrovascular disease" }, { "code": "QE70.Z", "title": "Problems related to primary support group, including family circumstances, unspecified" }, { "code": "8D6Y", "title": "Other specified disorders of cerebrospinal fluid pressure or flow" }, { "code": "LA8E.1", "title": "Atrial septal defect within oval fossa" }, { "code": "GA10.CZ", "title": "Endometriosis of unspecified site within the digestive system" }, { "code": "GA10.CY", "title": "Endometriosis of other sites within the digestive system" } ]
=== ICD-11 CODES FOUND === [LA8Y] Other specified structural developmental anomaly of heart or great vessels Also known as: Other specified structural developmental anomaly of heart or great vessels | Congenital anomaly of position or spatial relationships of thoraco-abdominal organs | Usual atrial arrangement | atrial situs solitus | Abnormal atrial arrangement [8B10.Y] Other specified transient ischaemic attack Also known as: Other specified transient ischaemic attack | Vertebrobasilar artery syndrome | vertebrobasilar arterial insufficiency | vertebrobasilar insufficiency | vertebro-basilar artery syndrome, course of resolution unspecified [6A80] Symptomatic and course presentations for mood episodes in mood disorders Definition: These categories may be applied to describe the presentation and characteristics of mood episodes in the context of single episode depressive disorder, recurrent depressive disorder, bipolar type I disorder, or bipolar type II disorder. These categories indicate the presence of specific, important features of the clinical presentation or of the course, onset, and pattern of mood episodes. These categories are not mutually exclusive, and as many may be added as apply. Also known as: Symptomatic and course presentations for mood episodes in mood disorders [LA8C.1] Anomalous aortic origin or course of coronary artery Definition: A congenital cardiovascular malformation in which the origin and/or course of a coronary artery is abnormal. This is where coronary "anomalies" in the presence of discordant ventriculo-arterial connections should be coded. Also known as: Anomalous aortic origin or course of coronary artery | Anomalous aortic origin of coronary artery with ventriculo-arterial concordance | Anomalous aortic origin of coronary artery | AAOCA - [Anomalous aortic origin of coronary artery] | Right coronary artery from left aortic sinus with ventriculo-arterial concordance [8B22.Y] Other specified cerebrovascular disease Also known as: Other specified cerebrovascular disease | Posterior reversible encephalopathy | Multiple or bilateral precerebral artery syndromes | multiple or bilateral precerebral artery syndromes, course of resolution unspecified | precerebral artery insufficiency NOS [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 [8D6Y] Other specified disorders of cerebrospinal fluid pressure or flow Also known as: Other specified disorders of cerebrospinal fluid pressure or flow | Cystic cerebrospinal fluid collection | Cerebrospinal fluid collection due to spinal intradural arachnoid cyst | Leptomeningeal cyst | Tarlov cyst [LA8E.1] Atrial septal defect within oval fossa Definition: A congenital cardiovascular malformation in which there is an interatrial communication confined to the region of the oval fossa (fossa ovalis), most commonly due to a deficiency of the primary atrial septum (septum primum) but deficiency of the septum secundum (superior interatrial fold) may also contribute. Also known as: Atrial septal defect within oval fossa | Ostium secundum atrial septal defect | Secundum atrial septal defect [GA10.CZ] Endometriosis of unspecified site within the digestive system Also known as: Endometriosis of unspecified site within the digestive system | Endometriosis of the digestive system [GA10.CY] Endometriosis of other sites within the digestive system Also known as: Endometriosis of other sites within the digestive system | Endometriosis of the liver === GRAPH WALKS === --- Walk 1 --- [LA8Y] Other specified structural developmental anomaly of heart or great vessels --PARENT--> [?] Structural developmental anomaly of heart or great vessels Def: A congenital malformation of the heart and/or great vessels or an acquired abnormality unique to the congenitally malformed heart.... --RELATED_TO--> [?] Congenital great vessel related acquired abnormality Def: Any postnatal pathological change in form or function of the heart and/or great vessels consequent to the presence of congenital cardiovascular disease.... --- Walk 2 --- [LA8Y] Other specified structural developmental anomaly of heart or great vessels --PARENT--> [?] Structural developmental anomaly of heart or great vessels Def: A congenital malformation of the heart and/or great vessels or an acquired abnormality unique to the congenitally malformed heart.... --CHILD--> [LA82] Total mirror imagery Def: A congenital malformation in which there is complete mirror-imaged arrangement of the internal organs along the left-right axis of the body.... --- Walk 3 --- [8B10.Y] Other specified transient ischaemic attack --PARENT--> [8B10] Transient ischaemic attack Def: Transient episode of focal neurological dysfunction caused by focal brain ischemia without acute infarction in the clinically relevant area of the brain or transient monocular visual loss due to retin... --CHILD--> [8B10.0] Amaurosis fugax Def: A transient episode of acute visual dysfunction caused by retinal ischaemia. Symptoms should resolve completely within 24 hours.... --- Walk 4 --- [8B10.Y] Other specified transient ischaemic attack --PARENT--> [8B10] Transient ischaemic attack Def: Transient episode of focal neurological dysfunction caused by focal brain ischemia without acute infarction in the clinically relevant area of the brain or transient monocular visual loss due to retin... --PARENT--> [?] Cerebral ischaemia --- Walk 5 --- [6A80] Symptomatic and course presentations for mood episodes in mood disorders Def: These categories may be applied to describe the presentation and characteristics of mood episodes in the context of single episode depressive disorder, recurrent depressive disorder, bipolar type I di... --RELATED_TO--> [?] 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, ... --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... --- Walk 6 --- [6A80] Symptomatic and course presentations for mood episodes in mood disorders Def: These categories may be applied to describe the presentation and characteristics of mood episodes in the context of single episode depressive disorder, recurrent depressive disorder, bipolar type I di... --PARENT--> [?] Mood disorders Def: Mood Disorders refers to a superordinate grouping of Bipolar and Depressive Disorders. Mood disorders are defined according to particular types of mood episodes and their pattern over time. The primar... --CHILD--> [6A80] Symptomatic and course presentations for mood episodes in mood disorders Def: These categories may be applied to describe the presentation and characteristics of mood episodes in the context of single episode depressive disorder, recurrent depressive disorder, bipolar type I di...
[ "[LA8Y] Other specified structural developmental anomaly of heart or great vessels\n --PARENT--> [?] Structural developmental anomaly of heart or great vessels\n Def: A congenital malformation of the heart and/or great vessels or an acquired abnormality unique to the congenitally malformed heart....\n --RELATED_TO--> [?] Congenital great vessel related acquired abnormality\n Def: Any postnatal pathological change in form or function of the heart and/or great vessels consequent to the presence of congenital cardiovascular disease....", "[LA8Y] Other specified structural developmental anomaly of heart or great vessels\n --PARENT--> [?] Structural developmental anomaly of heart or great vessels\n Def: A congenital malformation of the heart and/or great vessels or an acquired abnormality unique to the congenitally malformed heart....\n --CHILD--> [LA82] Total mirror imagery\n Def: A congenital malformation in which there is complete mirror-imaged arrangement of the internal organs along the left-right axis of the body....", "[8B10.Y] Other specified transient ischaemic attack\n --PARENT--> [8B10] Transient ischaemic attack\n Def: Transient episode of focal neurological dysfunction caused by focal brain ischemia without acute infarction in the clinically relevant area of the brain or transient monocular visual loss due to retin...\n --CHILD--> [8B10.0] Amaurosis fugax\n Def: A transient episode of acute visual dysfunction caused by retinal ischaemia. Symptoms should resolve completely within 24 hours....", "[8B10.Y] Other specified transient ischaemic attack\n --PARENT--> [8B10] Transient ischaemic attack\n Def: Transient episode of focal neurological dysfunction caused by focal brain ischemia without acute infarction in the clinically relevant area of the brain or transient monocular visual loss due to retin...\n --PARENT--> [?] Cerebral ischaemia", "[6A80] Symptomatic and course presentations for mood episodes in mood disorders\n Def: These categories may be applied to describe the presentation and characteristics of mood episodes in the context of single episode depressive disorder, recurrent depressive disorder, bipolar type I di...\n --RELATED_TO--> [?] 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, ...\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...", "[6A80] Symptomatic and course presentations for mood episodes in mood disorders\n Def: These categories may be applied to describe the presentation and characteristics of mood episodes in the context of single episode depressive disorder, recurrent depressive disorder, bipolar type I di...\n --PARENT--> [?] Mood disorders\n Def: Mood Disorders refers to a superordinate grouping of Bipolar and Depressive Disorders. Mood disorders are defined according to particular types of mood episodes and their pattern over time. The primar...\n --CHILD--> [6A80] Symptomatic and course presentations for mood episodes in mood disorders\n Def: These categories may be applied to describe the presentation and characteristics of mood episodes in the context of single episode depressive disorder, recurrent depressive disorder, bipolar type I di..." ]
LA8Y
Other specified structural developmental anomaly of heart or great vessels
[ { "from_icd11": "LA8Y", "icd10_code": "Q248 ", "icd10_title": "" }, { "from_icd11": "QE70.Z", "icd10_code": "Z6379", "icd10_title": "Other stressful life events affecting family and household" }, { "from_icd11": "QE70.Z", "icd10_code": "Z6372", "icd10_title": "Alcoholism and drug addiction in family" }, { "from_icd11": "QE70.Z", "icd10_code": "Z638", "icd10_title": "Other specified problems related to primary support group" }, { "from_icd11": "QE70.Z", "icd10_code": "Z639", "icd10_title": "Problem related to primary support group, unspecified" }, { "from_icd11": "QE70.Z", "icd10_code": "Z637", "icd10_title": "Other stressful life events affecting family and household" }, { "from_icd11": "LA8E.1", "icd10_code": "Q211", "icd10_title": "Atrial septal defect" } ]
Q248
The infant was transferred to the general paediatric ward on Day 5 and discharged home on Day 26. Initially, he was treated with a regimen of basal and rapid insulin and then transitioned to an insulin pump. L‐Thyroxine treatment was stopped at 1 month with normalization of the thyroid balance (TSH 0.21 μUI/ml; T4 10.6 pg/ml); without any antibodies stating a transient acute central hypothyroidism; and diabetes was well balanced. Chromosomal analysis by CGH‐Array was normal and the search for fragile X syndrome was negative. The metabolic workup was unremarkable (mucopolysaccharides, urinary oligosaccharides, plasma lysosphingolipids and Gaucher disease). In addition, the mitochondrial DNA study was normal. He was treated with anticoagulants (antivitamin K: coumadin 2 mg per day) for 3 months. The brain MRI performed at 3 months showed partial repermeabilization of the superior sagittal sinus with persistence of a heterogeneous aspect of the sinus, seat of some linear images probably corresponding to residual filiform thrombi, a complete repermeabilization of the transverse sinuses and the torcular and cortical veins, and an appearance of FLAIR signal abnormalities of the periventricular white matter, probably sequelae of the abnormalities visualized in diffusion on the first MRI . The neurological examination returned to baseline, and he is followed up in a specialized neurodevelopment centre.
3.939453
0.979492
sec[1]/p[5]
en
0.999997
36722309
https://doi.org/10.1002/edm2.389
[ "treated", "insulin", "repermeabilization", "sinus", "probably", "abnormalities", "transferred", "general", "paediatric", "ward" ]
[ { "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": "CA0A.Z", "title": "Chronic rhinosinusitis, unspecified" }, { "code": "CA0Y&XA3523", "title": "Nasal sinus obstruction" }, { "code": "CA0J.Y", "title": "Other specified nasal polyp" }, { "code": "LB03.Y", "title": "Other specified structural developmental anomalies of umbilical cord" }, { "code": "DA09.61", "title": "Periapical abscess with sinus" } ]
=== 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 [CA0A.Z] Chronic rhinosinusitis, unspecified Also known as: Chronic rhinosinusitis, unspecified | Chronic rhinosinusitis | Chronic sinusitis | chronic sinusitis NOS | unspecified sinusitis [CA0J.Y] Other specified nasal polyp Also known as: Other specified nasal polyp | Polyp of nasal cavity | Polyp of the nasopharynx | nasopharyngeal polyp | Polyp of adenoid tissue [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 [DA09.61] Periapical abscess with sinus Also known as: Periapical abscess with sinus | Dental abscess with sinus | Dentoalveolar abscess with sinus | Dental sinus | periapical abscess fistula Includes: Dental abscess with sinus | Dentoalveolar abscess with sinus | Dental sinus === GRAPH WALKS === --- Walk 1 --- [5A44] Insulin-resistance syndromes --PARENT--> [?] Other disorders of glucose regulation or pancreatic internal secretion --RELATED_TO--> [?] VIPoma Def: An often clinically aggressive neuroendocrine tumour located in the pancreas or small intestine. It is composed of cells containing vasoactive intestinal peptide. It may cause intractable diarrhea and... --- Walk 2 --- [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 3 --- [5A4Y] Other specified disorders of glucose regulation or pancreatic internal secretion --PARENT--> [?] Other disorders of glucose regulation or pancreatic internal secretion --EXCLUDES--> [?] Benign neoplasm of endocrine pancreas --- Walk 4 --- [5A4Y] Other specified disorders of glucose regulation or pancreatic internal secretion --PARENT--> [?] Other disorders of glucose regulation or pancreatic internal secretion --EXCLUDES--> [?] Multiple endocrine neoplasia type 1 Def: Multiple Endocrine Neoplasia type 1 (MEN1) is a rare hereditary cancer syndrome marked mainly by tumours of the parathyroids, endocrine pancreas and anterior pituitary, and characterised by a very hig... --- Walk 5 --- [QB51.5] Presence of endocrine implants --PARENT--> [QB51] Presence of devices other than cardiac or vascular implants --PARENT--> [?] Presence of device, implants or grafts --- 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--> [?] VIPoma\n Def: An often clinically aggressive neuroendocrine tumour located in the pancreas or small intestine. It is composed of cells containing vasoactive intestinal peptide. It may cause intractable diarrhea and...", "[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....", "[5A4Y] Other specified disorders of glucose regulation or pancreatic internal secretion\n --PARENT--> [?] Other disorders of glucose regulation or pancreatic internal secretion\n --EXCLUDES--> [?] Benign neoplasm of endocrine pancreas", "[5A4Y] Other specified disorders of glucose regulation or pancreatic internal secretion\n --PARENT--> [?] Other disorders of glucose regulation or pancreatic internal secretion\n --EXCLUDES--> [?] Multiple endocrine neoplasia type 1\n Def: Multiple Endocrine Neoplasia type 1 (MEN1) is a rare hereditary cancer syndrome marked mainly by tumours of the parathyroids, endocrine pancreas and anterior pituitary, and characterised by a very hig...", "[QB51.5] Presence of endocrine implants\n --PARENT--> [QB51] Presence of devices other than cardiac or vascular implants\n --PARENT--> [?] Presence of device, implants or grafts", "[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
A 66-year-old male was admitted to our hospital with an episode of chest pain during atrial fibrillation with rapid ventricular response following a month history of progressive exertional chest pain. He had been treated 15 years previously with two overlapping Duet 3.5 × 23 mm and 3.5 × 13 mm BMS to his proximal and mid right coronary artery. Electrocardiography did not show ischemic changes at rest, but a significant rise in cardiac biomarkers was noted, consistent with a diagnosis of non-ST-elevation myocardial infarction. Coronary angiography demonstrated a critical stenosis within the prior stent in the mid-RCA ( Figure 1(a) ) that was occlusive to flow when crossed with a Dragonfly Duo OCT catheter. Focal predilation of the severe stenosis was performed using a Trek 3.0 × 12 mm balloon to improve distal vessel flow. Subsequent OCT confirmed severe in-stent restenosis with a percent area stenosis of 78% and minimal luminal area of 2.3 mm 2 . OCT also revealed the presence of neoatherosclerosis with fibrocalcific plaque, lipid pools, macrophage accumulation, and neoangiogenesis (Figures 1(b) – 1(d) ) throughout the majority of the stent's length. A site of old plaque rupture was visualized within the stented segment neoatheroma ( Figure 1(e) ) with no evidence of acute thrombus. An incidental finding of malapposed uncovered struts at the proximal stent segment was also seen ( Figure 1(f) ).
4.050781
0.973633
sec[1]/p[0]
en
0.999996
27034852
https://doi.org/10.1155/2016/1652065
[ "stent", "stenosis", "chest", "pain", "coronary", "within", "flow", "area", "plaque", "segment" ]
[ { "code": "PK93.2", "title": "Gastroenterology or urology devices associated with injury or harm, prosthetic or other implants, materials or accessory devices" }, { "code": "QB51.1", "title": "Presence of urogenital implants" }, { "code": "QB51.Y", "title": "Presence of other specified devices other than cardiac or vascular implants" }, { "code": "QB51.3", "title": "Presence of otological or audiological implants" }, { "code": "PL12.3", "title": "Obstruction of device, as mode of injury or harm" }, { "code": "DB30.Y", "title": "Other specified obstruction of large intestine" }, { "code": "BB60.Z", "title": "Mitral valve stenosis, unspecified" }, { "code": "BD52.2", "title": "Stricture of artery" }, { "code": "FA82", "title": "Spinal stenosis" }, { "code": "DA40.0", "title": "Gastric outlet obstruction" } ]
=== ICD-11 CODES FOUND === [PK93.2] Gastroenterology or urology devices associated with injury or harm, prosthetic or other implants, materials or accessory devices Also known as: Gastroenterology or urology devices associated with injury or harm, prosthetic or other implants, materials or accessory devices | Surgical operation with implant of artificial internal gastroenterology or urology device associated with abnormal reaction of the patient, or of later complication, without mention of misadventure at the time of the procedure | Surgical operation with gastroenterological or urological bypass or graft associated with abnormal reaction of the patient, or of later complication, without mention of misadventure at the time of the procedure | Gastroenterology or urology devices associated with injury or harm, urethral or ureteral stents | Incrustation or calcification of indwelling ureteral stents Excludes: Circumstances associated with a surgical or other medical device influencing the episode of care without injury or harm [QB51.1] Presence of urogenital implants Also known as: Presence of urogenital implants | Presence of bladder implant | bladder replaced by other means | replacement of bladder by artificial or mechanical device or prosthesis | Presence of urethral stent [QB51.Y] Presence of other specified devices other than cardiac or vascular implants Also known as: Presence of other specified devices other than cardiac or vascular implants | Presence of bone or tendon implants other than orthopaedic joint implants | replacement of tendon by artificial or mechanical device or prosthesis | presence of tendon implant | Presence of skull plate [QB51.3] Presence of otological or audiological implants Also known as: Presence of otological or audiological implants | presence of audiological implant | presence of hearing device implant | presence of hearing-aid implant | presence of otological implant [PL12.3] Obstruction of device, as mode of injury or harm Definition: Obstruction associated with prosthetic devices, grafts or implants Also known as: Obstruction of device, as mode of injury or harm | occlusion shunt | blockage of device causing obstruction as mode of injury | blocked tube causing obstruction as mode of injury | occlusion of device causing obstruction as mode of injury Excludes: Obstruction of device without injury or harm [DB30.Y] Other specified obstruction of large intestine Also known as: Other specified obstruction of large intestine | Obstruction of large intestine due to compression or stenosis | Acute bowel obstruction, not elsewhere classified | Subacute bowel obstruction, not elsewhere classified | subacute intestinal obstruction NOS [BB60.Z] Mitral valve stenosis, unspecified Also known as: Mitral valve stenosis, unspecified | Mitral valve stenosis | MS - [mitral stenosis] | mitral stenosis | mitral valvular stricture [BD52.2] Stricture of artery Also known as: Stricture of artery | arterial stenosis | arterial stricture | artery stricture | stenosis of artery [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 [DA40.0] Gastric outlet obstruction Definition: Gastric outlet obstruction is a disorder characterised by epigastric abdominal pain and postprandial vomiting due to mechanical obstruction mostly at the level of the pylorus. Also known as: Gastric outlet obstruction | Adult hypertrophic pyloric stenosis | gastric outflow obstruction | hypertrophic pylorus stenosis | hypertrophic pylorus stricture === GRAPH WALKS === --- Walk 1 --- [PK93.2] Gastroenterology or urology devices associated with injury or harm, prosthetic or other implants, materials or accessory devices --PARENT--> [PK93] Gastroenterology or urology devices, implants or grafts associated with injury or harm --CHILD--> [PK93.1] Gastroenterology or urology devices associated with injury or harm, therapeutic, nonsurgical or rehabilitative devices Def: A gastroenterology or urology device was involved in an adverse incident that occurred in a therapeutic (nonsurgical) and rehabilitative task... --- Walk 2 --- [PK93.2] Gastroenterology or urology devices associated with injury or harm, prosthetic or other implants, materials or accessory devices --EXCLUDES--> [?] Circumstances associated with a surgical or other medical device influencing the episode of care without injury or harm --EXCLUDES--> [?] Mode of injury or harm associated with a surgical or other medical device, implant or graft --- Walk 3 --- [QB51.1] Presence of urogenital implants --PARENT--> [QB51] Presence of devices other than cardiac or vascular implants --EXCLUDES--> [?] Fitting, adjustment or management of devices --- Walk 4 --- [QB51.1] Presence of urogenital implants --PARENT--> [QB51] Presence of devices other than cardiac or vascular implants --CHILD--> [QB51.2] Presence of intraocular lens --- Walk 5 --- [QB51.Y] Presence of other specified devices other than cardiac or vascular implants --PARENT--> [QB51] Presence of devices other than cardiac or vascular implants --CHILD--> [QB51.0] Presence of a neurostimulator --- Walk 6 --- [QB51.Y] Presence of other specified devices other than cardiac or vascular implants --PARENT--> [QB51] Presence of devices other than cardiac or vascular implants --PARENT--> [?] Presence of device, implants or grafts
[ "[PK93.2] Gastroenterology or urology devices associated with injury or harm, prosthetic or other implants, materials or accessory devices\n --PARENT--> [PK93] Gastroenterology or urology devices, implants or grafts associated with injury or harm\n --CHILD--> [PK93.1] Gastroenterology or urology devices associated with injury or harm, therapeutic, nonsurgical or rehabilitative devices\n Def: A gastroenterology or urology device was involved in an adverse incident that occurred in a therapeutic (nonsurgical) and rehabilitative task...", "[PK93.2] Gastroenterology or urology devices associated with injury or harm, prosthetic or other implants, materials or accessory devices\n --EXCLUDES--> [?] Circumstances associated with a surgical or other medical device influencing the episode of care without injury or harm\n --EXCLUDES--> [?] Mode of injury or harm associated with a surgical or other medical device, implant or graft", "[QB51.1] Presence of urogenital implants\n --PARENT--> [QB51] Presence of devices other than cardiac or vascular implants\n --EXCLUDES--> [?] Fitting, adjustment or management of devices", "[QB51.1] Presence of urogenital implants\n --PARENT--> [QB51] Presence of devices other than cardiac or vascular implants\n --CHILD--> [QB51.2] Presence of intraocular lens", "[QB51.Y] Presence of other specified devices other than cardiac or vascular implants\n --PARENT--> [QB51] Presence of devices other than cardiac or vascular implants\n --CHILD--> [QB51.0] Presence of a neurostimulator", "[QB51.Y] Presence of other specified devices other than cardiac or vascular implants\n --PARENT--> [QB51] Presence of devices other than cardiac or vascular implants\n --PARENT--> [?] Presence of device, implants or grafts" ]
PK93.2
Gastroenterology or urology devices associated with injury or harm, prosthetic or other implants, materials or accessory devices
[ { "from_icd11": "PK93.2", "icd10_code": "T83711A", "icd10_title": "Erosion of implanted vaginal mesh to surrounding organ or tissue, initial encounter" }, { "from_icd11": "PK93.2", "icd10_code": "T83718A", "icd10_title": "Erosion of other implanted mesh to organ or tissue, initial encounter" }, { "from_icd11": "PK93.2", "icd10_code": "T83728A", "icd10_title": "Exposure of other implanted mesh into organ or tissue, initial encounter" }, { "from_icd11": "PK93.2", "icd10_code": "T83719A", "icd10_title": "Erosion of other prosthetic materials to surrounding organ or tissue, initial encounter" }, { "from_icd11": "PK93.2", "icd10_code": "T83718S", "icd10_title": "Erosion of other implanted mesh to organ or tissue, sequela" }, { "from_icd11": "PK93.2", "icd10_code": "T83712A", "icd10_title": "Erosion of implanted urethral mesh to surrounding organ or tissue, initial encounter" }, { "from_icd11": "PK93.2", "icd10_code": "T83721A", "icd10_title": "Exposure of implanted vaginal mesh into vagina, initial encounter" }, { "from_icd11": "PK93.2", "icd10_code": "T85590A", "icd10_title": "Other mechanical complication of bile duct prosthesis, initial encounter" }, { "from_icd11": "PK93.2", "icd10_code": "T83490A", "icd10_title": "Other mechanical complication of implanted penile prosthesis, initial encounter" }, { "from_icd11": "PK93.2", "icd10_code": "T85598A", "icd10_title": "Other mechanical complication of other gastrointestinal prosthetic devices, implants and grafts, initial encounter" }, { "from_icd11": "PK93.2", "icd10_code": "T85528A", "icd10_title": "Displacement of other gastrointestinal prosthetic devices, implants and grafts, initial encounter" }, { "from_icd11": "PK93.2", "icd10_code": "T85520A", "icd10_title": "Displacement of bile duct prosthesis, initial encounter" }, { "from_icd11": "PK93.2", "icd10_code": "T83193A", "icd10_title": "Other mechanical complication of other urinary stent, initial encounter" }, { "from_icd11": "PK93.2", "icd10_code": "T83123A", "icd10_title": "Displacement of other urinary stents, initial encounter" }, { "from_icd11": "PK93.2", "icd10_code": "T83111A", "icd10_title": "Breakdown (mechanical) of implanted urinary sphincter, initial encounter" } ]
T83711A
Erosion of implanted vaginal mesh to surrounding organ or tissue, initial encounter
Before deciding to perform the islet alloautotransplantation, we discussed whether to treat the likely pancreas allograft rejection with a third round of methylprednisolone and a postponed second-line treatment for chronic (or mixed-type) ABMR, which consists of alemtuzumab, plasma exchange, and/or IVIg at our center. Viral complications (BK-viremia, COVID-19) had prohibited escalation before. However, we felt that efficacy of such therapy for longer-standing chronic active perhaps antibody-mediated pancreas rejection would be questionable and that, given the progressive complications (panniculitis) necessitating chronic use of opioids, a more definite solution was warranted. The persistent immunodominant HLA-DSA DQB1*05:02-DQA1*01:02 at 1 year post-islet alloautotransplantation suggests indeed that second-line treatment would not have made the DSA disappear. Although speculative, we also hypothesized that taking away the subsisting inflammatory stimulus (exocrine tissue rejection/pancreatitis) would likely increase the chance of a more sustained response to novel induction treatment and better preserve his kidney function considering his highly-immunized status . A limitation of this point of view is that an auto-immune etiology of his type-1 diabetes could not be established (no detectable auto-antibodies), which might have contributed to a more favorable outcome of the islet transplantation.
4.148438
0.517578
sec[2]/p[2]
en
0.999994
37692453
https://doi.org/10.3389/ti.2023.11505
[ "that", "islet", "rejection", "alloautotransplantation", "likely", "pancreas", "line", "type", "which", "complications" ]
[ { "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": "2E92.9", "title": "Benign neoplasm of endocrine pancreas" }, { "code": "5A4Y", "title": "Other specified disorders of glucose regulation or pancreatic internal secretion" }, { "code": "2C10.1", "title": "Neuroendocrine neoplasms of pancreas" }, { "code": "2D81", "title": "Malignant neoplasm metastasis in pancreas" }, { "code": "2C10.Y", "title": "Other specified malignant neoplasms of pancreas" } ]
=== 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 [2E92.9] Benign neoplasm of endocrine pancreas Also known as: Benign neoplasm of endocrine pancreas | benign neoplasm of islets of Langerhans | islet cell adenoma of unspecified site | islet cell neoplasm | islet cell pancreatic adenoma Includes: Islet cell tumour | benign neoplasm of islets of Langerhans [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 [2C10.1] Neuroendocrine neoplasms of pancreas Definition: A neoplasm with neuroendocrine differentiation that arises from the pancreas. It includes neuroendocrine tumours (low and intermediate grade) and neuroendocrine carcinomas (high grade). Also known as: Neuroendocrine neoplasms of pancreas | neuroendocrine pancreatic cancer | carcinoma of islet cell of pancreas | malignant islet cell tumour of unspecified site | malignant tumour, islet cell of pancreas [2D81] Malignant neoplasm metastasis in pancreas Definition: A malignant neoplasm that has spread to the pancreas from another anatomic site. Representative examples include metastatic carcinomas from the gastrointestinal tract, metastatic melanomas, and renal cell carcinomas. Also known as: Malignant neoplasm metastasis in pancreas | pancreas metastasis | pancreatic islet cells metastasis | pancreatic metastasis | secondary malignant deposit in pancreas [2C10.Y] Other specified malignant neoplasms of pancreas Also known as: Other specified malignant neoplasms of pancreas | Familial pancreatic carcinoma | Metastatic pancreatic carcinoma [primary pancreatic carcinoma spreading elsewhere] | metastatic pancreas carcinoma [primary pancreatic carcinoma spreading elsewhere] | Pancreatic carcinoma === GRAPH WALKS === --- Walk 1 --- [8A80.Z] Migraine, unspecified --PARENT--> [8A80] Migraine Def: A primary headache disorder, in most cases episodic. Disabling attacks lasting 4-72 hours are characterised by moderate or severe headache, usually accompanied by nausea, vomiting and/or photophobia a... --PARENT--> [?] Headache disorders --- Walk 2 --- [8A80.Z] Migraine, unspecified --PARENT--> [8A80] Migraine Def: A primary headache disorder, in most cases episodic. Disabling attacks lasting 4-72 hours are characterised by moderate or severe headache, usually accompanied by nausea, vomiting and/or photophobia a... --CHILD--> [8A80.1] Migraine with aura Def: Recurrent attacks, lasting minutes, of unilateral fully-reversible visual, sensory or other central nervous system symptoms that usually develop gradually and are usually followed by headache and asso... --- Walk 3 --- [QA76] Medication or substance that is known to be an allergen without injury or harm Def: Medication that has previously been identified as an allergen to the patient is administered, but does not result in injury or harm.... --EXCLUDES--> [?] Medication or substance that is known to be an allergen, as mode of injury or harm --PARENT--> [?] Mode of injury or harm associated with exposure to a drug, medicament or biological substance --- Walk 4 --- [QA76] Medication or substance that is known to be an allergen without injury or harm Def: Medication that has previously been identified as an allergen to the patient is administered, but does not result in injury or harm.... --EXCLUDES--> [?] Medication or substance that is known to be an allergen, as mode of injury or harm --PARENT--> [?] Mode of injury or harm associated with exposure to a drug, medicament or biological substance --- Walk 5 --- [PL13.6] Medication or substance that is known to be an allergen, as mode of injury or harm --PARENT--> [PL13] Mode of injury or harm associated with exposure to a drug, medicament or biological substance --CHILD--> [PL13.1] Underdosing, as mode of injury or harm --- Walk 6 --- [PL13.6] Medication or substance that is known to be an allergen, as mode of injury or harm --PARENT--> [PL13] Mode of injury or harm associated with exposure to a drug, medicament or biological substance --CHILD--> [PL13.1] Underdosing, as mode of injury or harm
[ "[8A80.Z] Migraine, unspecified\n --PARENT--> [8A80] Migraine\n Def: A primary headache disorder, in most cases episodic. Disabling attacks lasting 4-72 hours are characterised by moderate or severe headache, usually accompanied by nausea, vomiting and/or photophobia a...\n --PARENT--> [?] Headache disorders", "[8A80.Z] Migraine, unspecified\n --PARENT--> [8A80] Migraine\n Def: A primary headache disorder, in most cases episodic. Disabling attacks lasting 4-72 hours are characterised by moderate or severe headache, usually accompanied by nausea, vomiting and/or photophobia a...\n --CHILD--> [8A80.1] Migraine with aura\n Def: Recurrent attacks, lasting minutes, of unilateral fully-reversible visual, sensory or other central nervous system symptoms that usually develop gradually and are usually followed by headache and asso...", "[QA76] Medication or substance that is known to be an allergen without injury or harm\n Def: Medication that has previously been identified as an allergen to the patient is administered, but does not result in injury or harm....\n --EXCLUDES--> [?] Medication or substance that is known to be an allergen, as mode of injury or harm\n --PARENT--> [?] Mode of injury or harm associated with exposure to a drug, medicament or biological substance", "[QA76] Medication or substance that is known to be an allergen without injury or harm\n Def: Medication that has previously been identified as an allergen to the patient is administered, but does not result in injury or harm....\n --EXCLUDES--> [?] Medication or substance that is known to be an allergen, as mode of injury or harm\n --PARENT--> [?] Mode of injury or harm associated with exposure to a drug, medicament or biological substance", "[PL13.6] Medication or substance that is known to be an allergen, as mode of injury or harm\n --PARENT--> [PL13] Mode of injury or harm associated with exposure to a drug, medicament or biological substance\n --CHILD--> [PL13.1] Underdosing, as mode of injury or harm", "[PL13.6] Medication or substance that is known to be an allergen, as mode of injury or harm\n --PARENT--> [PL13] Mode of injury or harm associated with exposure to a drug, medicament or biological substance\n --CHILD--> [PL13.1] Underdosing, as mode of injury or harm" ]
8A80.Z
Migraine, unspecified
[ { "from_icd11": "8A80.Z", "icd10_code": "G43B0", "icd10_title": "Ophthalmoplegic migraine, not intractable" }, { "from_icd11": "8A80.Z", "icd10_code": "G43409", "icd10_title": "Hemiplegic migraine, not intractable, without status migrainosus" }, { "from_icd11": "8A80.Z", "icd10_code": "G43A0", "icd10_title": "Cyclical vomiting, in migraine, not intractable" }, { "from_icd11": "8A80.Z", "icd10_code": "G43D0", "icd10_title": "Abdominal migraine, not intractable" }, { "from_icd11": "8A80.Z", "icd10_code": "G43709", "icd10_title": "Chronic migraine without aura, not intractable, without status migrainosus" }, { "from_icd11": "8A80.Z", "icd10_code": "G43A1", "icd10_title": "Cyclical vomiting, in migraine, intractable" }, { "from_icd11": "8A80.Z", "icd10_code": "G43509", "icd10_title": "Persistent migraine aura without cerebral infarction, not intractable, without status migrainosus" }, { "from_icd11": "8A80.Z", "icd10_code": "G43719", "icd10_title": "Chronic migraine without aura, intractable, without status migrainosus" }, { "from_icd11": "8A80.Z", "icd10_code": "G43501", "icd10_title": "Persistent migraine aura without cerebral infarction, not intractable, with status migrainosus" }, { "from_icd11": "8A80.Z", "icd10_code": "G43C0", "icd10_title": "Periodic headache syndromes in child or adult, not intractable" }, { "from_icd11": "8A80.Z", "icd10_code": "G43401", "icd10_title": "Hemiplegic migraine, not intractable, with status migrainosus" }, { "from_icd11": "8A80.Z", "icd10_code": "G43419", "icd10_title": "Hemiplegic migraine, intractable, without status migrainosus" }, { "from_icd11": "8A80.Z", "icd10_code": "G43B1", "icd10_title": "Ophthalmoplegic migraine, intractable" }, { "from_icd11": "8A80.Z", "icd10_code": "G43C1", "icd10_title": "Periodic headache syndromes in child or adult, intractable" }, { "from_icd11": "8A80.Z", "icd10_code": "G43D1", "icd10_title": "Abdominal migraine, intractable" } ]
G43B0
Ophthalmoplegic migraine, not intractable
A clinical examination revealed a first to second degree multinodular goiter, which was mobile, soft and not painful on palpation. There was no palpable lymphadenopathy in the neck. Thyroid function tests showed a hypothyroidism state: Increased thyrotropic-stimulating hormone [TSH; 6.12 μIU/ml; normal range (NR), 0.35–5.5 μIU/ml] and antithyroglobulin antibody levels (27.8 IU/ml; NR, ≤4.11 IU/ml); decreased free triiodothyronine (2.96 pmol/l; NR, 3.0–6.51 pmol/l) and triiodothyronine (0.9 nmol/l; NR, 0.92–2.79 nmol/l) concentrations; normal thyroxine and free thyroxine, thyroglobulin and thyroid-binding globulin levels; and a negative result for antithyroperoxidase antibody. Biochemical analyses only showed elevated C-reactive protein levels (31.44 mg/l; NR, ≤8 mg/l). Thyroid B-mode ultrasonographyrevealed a number of hypoechoic nodules in the bilateral lobe of the thyroid gland, with sizes varying between 5 and 11 mm. However, one of these nodules (7–8 mm in size) located near the top of the left thyroid lobe was a heterogeneous hypoechoic lesion, and infiltrative margins with microcalcifications were identified by ultrasonography . B-mode ultrasonography showed a malignant nodule and cervical lymphadenectasis. Computed tomography revealed that the cervical lymphonodule was enlarged on the left side, at levels III and IV . The chest X-ray was normal and other extrapulmonary TBs were excluded.
4.042969
0.969238
sec[1]/p[1]
en
0.999997
24765176
https://doi.org/10.3892/ol.2014.1901
[ "thyroid", "antibody", "free", "triiodothyronine", "pmol", "nmol", "thyroxine", "mode", "hypoechoic", "nodules" ]
[ { "code": "5A03.Z", "title": "Thyroiditis, unspecified" }, { "code": "5A0Z", "title": "Disorders of the thyroid gland or thyroid hormones system, unspecified" }, { "code": "5A03.Y", "title": "Other specified thyroiditis" }, { "code": "5A00.2Z", "title": "Acquired hypothyroidism, unspecified" }, { "code": "5A03.0", "title": "Acute thyroiditis" }, { "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 === [5A03.Z] Thyroiditis, unspecified Also known as: Thyroiditis, unspecified | Thyroiditis | inflammation of thyroid | thyroiditis NOS [5A0Z] Disorders of the thyroid gland or thyroid hormones system, unspecified Also known as: Disorders of the thyroid gland or thyroid hormones system, unspecified [5A03.Y] Other specified thyroiditis Also known as: Other specified thyroiditis | Riedel thyroiditis | Chronic invasive fibrous thyroiditis | Ligneous thyroiditis | Riedel struma [5A00.2Z] Acquired hypothyroidism, unspecified Also known as: Acquired hypothyroidism, unspecified | Acquired hypothyroidism | hypothyrea | thyroid insufficiency | hypothyroidea [5A03.0] Acute thyroiditis Definition: Acute thyroiditis is a rare form of thyroiditis directly caused by an infection, frequently bacterial. Also known as: Acute thyroiditis | infectious thyroiditis | Acute thyroiditis due to bacterial infection | Acute thyroiditis due to fungal infection | Abscess of thyroid [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 --- [5A03.Z] Thyroiditis, unspecified --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... --CHILD--> [5A03.1] Subacute thyroiditis Def: A self-limited thyroiditis associated with a triphasic clinical course of hyperthyroidism, hypothyroidism, and return to normal thyroid function. It is thought to be caused by a viral infection.... --- Walk 2 --- [5A03.Z] Thyroiditis, unspecified --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--> [?] Thyrotoxicosis Def: A hypermetabolic condition associated with elevated levels of free thyroxine and/or free triiodothyronine resulting in excess synthesis and secretion of thyroid hormone... --- Walk 3 --- [5A0Z] Disorders of the thyroid gland or thyroid hormones system, unspecified --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.... --CHILD--> [5A00] Hypothyroidism --- Walk 4 --- [5A0Z] Disorders of the thyroid gland or thyroid hormones system, unspecified --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.... --CHILD--> [5A02] Thyrotoxicosis Def: A hypermetabolic condition associated with elevated levels of free thyroxine and/or free triiodothyronine resulting in excess synthesis and secretion of thyroid hormone... --- Walk 5 --- [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... --RELATED_TO--> [?] Postpartum thyroiditis Def: Postpartum thyroiditis (PPT) is the occurrence, in the postpartum period, of transient hyperthyroidism and/or transient hypothyroidism, with most women returning to the euthyroid state by 1 year postp... --- Walk 6 --- [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... --RELATED_TO--> [?] Postpartum thyroiditis Def: Postpartum thyroiditis (PPT) is the occurrence, in the postpartum period, of transient hyperthyroidism and/or transient hypothyroidism, with most women returning to the euthyroid state by 1 year postp...
[ "[5A03.Z] Thyroiditis, unspecified\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 --CHILD--> [5A03.1] Subacute thyroiditis\n Def: A self-limited thyroiditis associated with a triphasic clinical course of hyperthyroidism, hypothyroidism, and return to normal thyroid function. It is thought to be caused by a viral infection....", "[5A03.Z] Thyroiditis, unspecified\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--> [?] Thyrotoxicosis\n Def: A hypermetabolic condition associated with elevated levels of free thyroxine and/or free triiodothyronine resulting in excess synthesis and secretion of thyroid hormone...", "[5A0Z] Disorders of the thyroid gland or thyroid hormones system, unspecified\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....\n --CHILD--> [5A00] Hypothyroidism", "[5A0Z] Disorders of the thyroid gland or thyroid hormones system, unspecified\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....\n --CHILD--> [5A02] Thyrotoxicosis\n Def: A hypermetabolic condition associated with elevated levels of free thyroxine and/or free triiodothyronine resulting in excess synthesis and secretion of thyroid hormone...", "[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 --RELATED_TO--> [?] Postpartum thyroiditis\n Def: Postpartum thyroiditis (PPT) is the occurrence, in the postpartum period, of transient hyperthyroidism and/or transient hypothyroidism, with most women returning to the euthyroid state by 1 year postp...", "[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 --RELATED_TO--> [?] Postpartum thyroiditis\n Def: Postpartum thyroiditis (PPT) is the occurrence, in the postpartum period, of transient hyperthyroidism and/or transient hypothyroidism, with most women returning to the euthyroid state by 1 year postp..." ]
5A03.Z
Thyroiditis, unspecified
[ { "from_icd11": "5A03.Z", "icd10_code": "E069", "icd10_title": "Thyroiditis, unspecified" }, { "from_icd11": "5A03.Z", "icd10_code": "E064", "icd10_title": "Drug-induced thyroiditis" }, { "from_icd11": "5A03.Z", "icd10_code": "E065", "icd10_title": "Other chronic thyroiditis" }, { "from_icd11": "5A03.Z", "icd10_code": "E06", "icd10_title": "Thyroiditis" }, { "from_icd11": "5A03.Z", "icd10_code": "E062", "icd10_title": "Chronic thyroiditis with transient thyrotoxicosis" }, { "from_icd11": "5A0Z", "icd10_code": "E0781", "icd10_title": "Sick-euthyroid syndrome" }, { "from_icd11": "5A0Z", "icd10_code": "E0789", "icd10_title": "Other specified disorders of thyroid" }, { "from_icd11": "5A0Z", "icd10_code": "E079", "icd10_title": "Disorder of thyroid, unspecified" }, { "from_icd11": "5A0Z", "icd10_code": "E034", "icd10_title": "Atrophy of thyroid (acquired)" }, { "from_icd11": "5A0Z", "icd10_code": "E00-E07", "icd10_title": "" }, { "from_icd11": "5A0Z", "icd10_code": "E07", "icd10_title": "Other disorders of thyroid" }, { "from_icd11": "5A0Z", "icd10_code": "E078", "icd10_title": "Other specified disorders of thyroid" }, { "from_icd11": "5A0Z", "icd10_code": "E35", "icd10_title": "Disorders of endocrine glands in diseases classified elsewhere" }, { "from_icd11": "5A00.2Z", "icd10_code": "E033", "icd10_title": "Postinfectious hypothyroidism" }, { "from_icd11": "5A03.0", "icd10_code": "E060", "icd10_title": "Acute thyroiditis" } ]
E069
Thyroiditis, unspecified
Techniques of diagnostic imaging are available if there is a clinical suspicion of splenogonadal fusion. The most reliable investigation to confirm its diagnosis is preoperative imaging through 99 m Tc-sulfur colloid liver spleen scan, which detects accessory spleen. Recently, Doppler ultrasonography of the scrotum of patients with a palpable testicular mass has been used to diagnose preoperatively few cases of splenogonadal fusion by visualizing a hypervascular mass on the upper pole of testis and comparing it with patient's own normally located spleen . Such use of this modality again depends on high index of suspicion in cases of splenogonadal fusion presenting as cryptorchidism, but it may be of value in patients presenting with acute scrotal lump. Unaware of the nature of the left scrotal masses, many surgeons have sacrificed an intact testis because they lacked a proper preoperative diagnosis. Surgeons ignorant of the nature of the scrotal mass and fearing malignant degeneration have performed radical orchidectomy on salvageable testes . In our cases, as the patient had primary gonadal failure and laparoscopic assessment was suggestive of benign testicular mass due to splenogonadal fusion with atrophic testis, so simple excision of mass was done. This highlights the importance of laparoscopic assessment for the nature of the mass, which saves the patient from undergoing a radical surgery.
4.15625
0.577148
sec[2]/p[2]
en
0.999997
24963439
https://doi.org/10.1155/2014/796761
[ "splenogonadal", "fusion", "spleen", "cases", "testis", "scrotal", "nature", "imaging", "suspicion", "preoperative" ]
[ { "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": "3B8Z", "title": "Diseases of spleen, unspecified" }, { "code": "LA8Z", "title": "Structural developmental anomaly of heart or great vessels, unspecified" }, { "code": "3B81.Y", "title": "Other specified acquired disorders of spleen" }, { "code": "LB22.Y", "title": "Other specified structural developmental anomalies of spleen" }, { "code": "3B81.2", "title": "Atrophy of spleen" } ]
=== 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 [3B8Z] Diseases of spleen, unspecified Also known as: Diseases of spleen, unspecified | splenic disease | splenopathy [LA8Z] Structural developmental anomaly of heart or great vessels, unspecified Also known as: Structural developmental anomaly of heart or great vessels, unspecified | Heart malformations | Cardiac malformations | congenital anomaly of heart | congenital heart disease [3B81.Y] Other specified acquired disorders of spleen Also known as: Other specified acquired disorders of spleen | Peliosis of spleen | Congestion of spleen | splenic congestion | Lymphoid hyperplasia of spleen [LB22.Y] Other specified structural developmental anomalies of spleen Also known as: Other specified structural developmental anomalies of spleen | Congenital malformation of spleen | malformations of spleen NOS | Aberrant spleen | Congenital lobulation of spleen [3B81.2] Atrophy of spleen Definition: A disease caused by determinants arising after birth, during the antenatal period or by genetically inherited factors. This disease is characterised by partial or complete degradation of the spleen. This disease may present with increased susceptibility to infection. Confirmation is through medical imaging. Also known as: Atrophy of spleen | hyposplenism | splenic atrophy | Hyposplenism due to previous infarction of spleen | Degenerative diseases of the spleen === 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--> [?] Ankylosis of spinal joint --CHILD--> [?] Ankylosis of lumbar spinal joint --- 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--> [LB17.2] 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 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--> [?] Ankylosis of spinal joint\n --CHILD--> [?] Ankylosis of lumbar spinal joint", "[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--> [LB17.2] 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...", "[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
The patient is a 35-year-old man, who is a chronic snorer with a BMI of 32.4 kg/m 2 who is not sleepy (Epworth Sleepiness Scale = 1/24). The patient's wife is a very light sleeper and is highly sensitive to snoring sounds. Over the past 14 years, the patient's weight has gone as high as 129.5 kg (BMI = 39.7 kg/m 2 ) and as low as 88.2 kg (BMI = 27.1 kg/m 2 ). The patient is known to have heroic snoring confirmed by his spouse for several years, when his BMI is above 100 kg (BMI = 30.7 kg/m 2 ); however, at weights below 100 kg, there is no snoring noted. The patient's current weight has been relatively unchanged (±1 kg) for the past year. History and physical exam demonstrate that the patient has no nasal septal deviation and no inferior turbinate hypertrophy (grade 2 bilaterally ) and has not had any complaints of nasal obstruction (NOSE questionnaire score = 10/100). After reviewing the literature for the variety of published modalities to abate snoring, the patient selected to utilize a previously unpublished technique for snoring, which is the use of a standard nasopharyngeal airway tube. This modality was selected since the patient has no nasal obstruction, septal deviation, or turbinate hypertrophy; therefore, the anatomy should be conducive to placement and use of NPAT. The sizes of soft polyvinyl chloride nasopharyngeal airway tubes evaluated included 24, 26, 28, 30, and 36 French (Fr).
3.865234
0.978516
sec[1]/p[1]
en
0.999998
27795710
https://doi.org/10.1155/2016/3628716
[ "snoring", "nasal", "past", "weight", "septal", "deviation", "turbinate", "hypertrophy", "obstruction", "selected" ]
[ { "code": "MD11.Y", "title": "Other specified abnormalities of breathing" }, { "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": "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" } ]
=== ICD-11 CODES FOUND === [MD11.Y] Other specified abnormalities of breathing Also known as: Other specified abnormalities of breathing | Bradypnoea | Choking sensation | Hypoventilation | hypoventilation syndrome NOS [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 [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 === GRAPH WALKS === --- Walk 1 --- [MD11.Y] Other specified abnormalities of breathing --PARENT--> [MD11] Abnormalities of breathing Def: Abnormalities of breathing includes dyspnoea, stridor, wheezing, periodic breathing, hyperventilation, mouth breathing, hiccough, sneezing, and other abnormalities of breathing.... --EXCLUDES--> [?] Respiratory distress of newborn Def: A condition characterised by developmental insufficiency of surfactant associated proteins or surfactant production and structural immaturity in the lungs.... --- Walk 2 --- [MD11.Y] Other specified abnormalities of breathing --PARENT--> [MD11] Abnormalities of breathing Def: Abnormalities of breathing includes dyspnoea, stridor, wheezing, periodic breathing, hyperventilation, mouth breathing, hiccough, sneezing, and other abnormalities of breathing.... --CHILD--> [MD11.1] Asphyxia Def: Asphyxia is a life-threatening condition in which oxygen is prevented from reaching the tissues by obstruction of or damage to any part of the respiratory system. More generally the term indicates all... --- Walk 3 --- [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--> [MA82.1] Dysphonia Def: Difficulty and/or pain in phonation or speaking.... --- Walk 4 --- [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 5 --- [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 ... --CHILD--> [CA01] Acute sinusitis Def: Recent onset and/or short duration inflammation of the mucosa in one or more of the paranasal sinuses (maxillary, ethmoid, frontal and sphenoid) arising from infection or other causes such as caries o... --- Walk 6 --- [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 ... --CHILD--> [CA00] Acute nasopharyngitis Def: A disease of the upper respiratory tract, caused by an infection with rhinovirus. This disease is characterised by pharyngitis, runny nose, stuffy nose, or cough. Transmission is by inhalation of infe...
[ "[MD11.Y] Other specified abnormalities of breathing\n --PARENT--> [MD11] Abnormalities of breathing\n Def: Abnormalities of breathing includes dyspnoea, stridor, wheezing, periodic breathing, hyperventilation, mouth breathing, hiccough, sneezing, and other abnormalities of breathing....\n --EXCLUDES--> [?] Respiratory distress of newborn\n Def: A condition characterised by developmental insufficiency of surfactant associated proteins or surfactant production and structural immaturity in the lungs....", "[MD11.Y] Other specified abnormalities of breathing\n --PARENT--> [MD11] Abnormalities of breathing\n Def: Abnormalities of breathing includes dyspnoea, stridor, wheezing, periodic breathing, hyperventilation, mouth breathing, hiccough, sneezing, and other abnormalities of breathing....\n --CHILD--> [MD11.1] Asphyxia\n Def: Asphyxia is a life-threatening condition in which oxygen is prevented from reaching the tissues by obstruction of or damage to any part of the respiratory system. More generally the term indicates all...", "[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--> [MA82.1] Dysphonia\n Def: Difficulty and/or pain in phonation or speaking....", "[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 --CHILD--> [CA01] Acute sinusitis\n Def: Recent onset and/or short duration inflammation of the mucosa in one or more of the paranasal sinuses (maxillary, ethmoid, frontal and sphenoid) arising from infection or other causes such as caries o...", "[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 --CHILD--> [CA00] Acute nasopharyngitis\n Def: A disease of the upper respiratory tract, caused by an infection with rhinovirus. This disease is characterised by pharyngitis, runny nose, stuffy nose, or cough. Transmission is by inhalation of infe..." ]
MD11.Y
Other specified abnormalities of breathing
[ { "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
A 68-year-old Japanese woman underwent barium follow-through examination for the upper gastrointestinal tract as part of a routine medical screening. A pedunculated polyp was detected in the duodenum . The patient was referred to our hospital for further investigation and treatment of the polyp. The patient had been taking medication for hyperlipidemia but had no history of gastrointestinal diseases. A physical examination revealed no abnormalities, and there was no evidence of peripheral lymphadenopathy. Laboratory findings revealed an elevated level of total cholesterol to 254 mg/dL, but levels of carcinoembryonic antigen and carbohydrate antigen 19-9 and blood cell counts were within normal ranges. Esophagogastroduodenoscopy showed a pedunculated polyp in the duodenal second portion. The head of the polyp was approximately 20 mm in size (Figures 2(a) and 2(b) ). There were no erosions or ulcers in the polyp. The tumor had long stalk; therefore it easily migrated to the stomach ( Figure 2(c) ). Magnifying observation with narrowband imaging confirmed that the surface was entirely covered with intact duodenal mucosa, suggesting a subepithelial origin of the tumor ( Figure 2(d) ). Endoscopic ultrasonography visualized at least three cystic structures in the polyp head (Figures 2(e) and 2(f) ). Based on the macroscopic and ultrasonography features, Brunner's gland hamartoma was highly suspected.
3.949219
0.974121
sec[1]/p[0]
en
0.999996
27579190
https://doi.org/10.1155/2016/6707235
[ "polyp", "gastrointestinal", "pedunculated", "antigen", "duodenal", "head", "figures", "tumor", "ultrasonography", "japanese" ]
[ { "code": "CA0J.Y", "title": "Other specified nasal polyp" }, { "code": "DB71.Z", "title": "Anal polyp, unspecified" }, { "code": "DA09.0", "title": "Pulpitis" }, { "code": "DB71.1", "title": "Lymphoid polyp" }, { "code": "GA16.Y", "title": "Other specified acquired abnormalities of uterus, except cervix" }, { "code": "DE2Z", "title": "Diseases of the digestive system, unspecified" }, { "code": "DB30.Y", "title": "Other specified obstruction of large intestine" }, { "code": "DA60.Y", "title": "Other specified gastric ulcer" }, { "code": "NB91.Y&XA9607", "title": "Gastrointestinal laceration" }, { "code": "DD90.3", "title": "Functional dyspepsia" } ]
=== ICD-11 CODES FOUND === [CA0J.Y] Other specified nasal polyp Also known as: Other specified nasal polyp | Polyp of nasal cavity | Polyp of the nasopharynx | nasopharyngeal polyp | Polyp of adenoid tissue [DB71.Z] Anal polyp, unspecified Also known as: Anal polyp, unspecified | Anal polyp [DA09.0] Pulpitis Definition: Inflammation of pulpal tissue resulting from irritating factors of diverse nature such as bacterial, hyperaemic, chemical or thermal that act directly or indirectly on the dental pulp. Also known as: Pulpitis | Pulpitis NOS | Suppurative pulpitis | Acute pulpitis | Chronic pulpitis Includes: Suppurative pulpitis [DB71.1] Lymphoid polyp Definition: Lymphoid polyp is a benign, focal or diffuse small polypoid lesion composed of well-differentiated lymphoid tissue. Also known as: Lymphoid polyp [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 [DE2Z] Diseases of the digestive system, unspecified Also known as: Diseases of the digestive system, unspecified | gastrointestinal disorder NOS | gastrointestinal disease NOS | digestive disorder NOS | digestive disturbance [DB30.Y] Other specified obstruction of large intestine Also known as: Other specified obstruction of large intestine | Obstruction of large intestine due to compression or stenosis | Acute bowel obstruction, not elsewhere classified | Subacute bowel obstruction, not elsewhere classified | subacute intestinal obstruction NOS [DA60.Y] Other specified gastric ulcer Also known as: Other specified gastric ulcer | Gastric ulcer due to diseases classified elsewhere | Gastric ulcer to due to other diseases, classified elsewhere | Gastric ulcer due to Crohn disease | Gastric ulcer due to sarcoidosis [DD90.3] Functional dyspepsia Definition: Functional dyspepsia is a disorder defined as the presence of dyspepsia symptoms thought to originate from the gastroduodenal region, in the absence of any organic, systemic, or metabolic disease that is likely to explain the symptoms such as epigastric pain, epigastric burning, postprandial fullness, and early satiation. Also known as: Functional dyspepsia | Indigestion | gastrointestinal distress | gastrointestinal disturbance | gastrointestinal irritation Includes: Indigestion | Postprandial distress syndrome Excludes: Heartburn | Dyspepsia NOS === GRAPH WALKS === --- Walk 1 --- [CA0J.Y] Other specified nasal polyp --PARENT--> [CA0J] Nasal polyp Def: Nasal polyp is an inflammatory and proliferating mass arising from the epithelial linings of nasal cavity and paranasal sinuses. In general, nasal polyp appears to be greyish white, smoothly surfaced,... --CHILD--> [CA0J.Z] Nasal polyp, unspecified --- Walk 2 --- [CA0J.Y] Other specified nasal polyp --PARENT--> [CA0J] Nasal polyp Def: Nasal polyp is an inflammatory and proliferating mass arising from the epithelial linings of nasal cavity and paranasal sinuses. In general, nasal polyp appears to be greyish white, smoothly surfaced,... --EXCLUDES--> [?] Benign neoplasm of middle ear, nasal cavity or accessory sinuses --- Walk 3 --- [DB71.Z] Anal polyp, unspecified --PARENT--> [DB71] Anal polyp Def: Abnormal mushroom-like growth sticking out from the epithelium rising from the lining of the anus and anal canal.... --CHILD--> [DB71.0] Inflammatory anal polyp Def: Inflammatory polyp is an abnormal, mushroom-like growth sticking out from the mucous membrane that lines the anus. This mass is a reaction to some type of chronic inflammation in the anus.... --- Walk 4 --- [DB71.Z] Anal polyp, unspecified --PARENT--> [DB71] Anal polyp Def: Abnormal mushroom-like growth sticking out from the epithelium rising from the lining of the anus and anal canal.... --CHILD--> [DB71.1] Lymphoid polyp Def: Lymphoid polyp is a benign, focal or diffuse small polypoid lesion composed of well-differentiated lymphoid tissue.... --- Walk 5 --- [DA09.0] Pulpitis Def: Inflammation of pulpal tissue resulting from irritating factors of diverse nature such as bacterial, hyperaemic, chemical or thermal that act directly or indirectly on the dental pulp.... --PARENT--> [DA09] Diseases of pulp or periapical tissues Def: Dental pulp is that part of the tooth located in the centre of the coronal portion underneath dentin and composed of connective tissue, blood vessels and nerve endings. Periapical tissues are designat... --CHILD--> [DA09.1] Necrosis of pulp Def: Necrosis of the dental pulp which clinically does not respond to thermal stimulation; the tooth may be asymptomatic or sensitive to percussion and palpation.... --- Walk 6 --- [DA09.0] Pulpitis Def: Inflammation of pulpal tissue resulting from irritating factors of diverse nature such as bacterial, hyperaemic, chemical or thermal that act directly or indirectly on the dental pulp.... --PARENT--> [DA09] Diseases of pulp or periapical tissues Def: Dental pulp is that part of the tooth located in the centre of the coronal portion underneath dentin and composed of connective tissue, blood vessels and nerve endings. Periapical tissues are designat... --CHILD--> [DA09.1] Necrosis of pulp Def: Necrosis of the dental pulp which clinically does not respond to thermal stimulation; the tooth may be asymptomatic or sensitive to percussion and palpation....
[ "[CA0J.Y] Other specified nasal polyp\n --PARENT--> [CA0J] Nasal polyp\n Def: Nasal polyp is an inflammatory and proliferating mass arising from the epithelial linings of nasal cavity and paranasal sinuses. In general, nasal polyp appears to be greyish white, smoothly surfaced,...\n --CHILD--> [CA0J.Z] Nasal polyp, unspecified", "[CA0J.Y] Other specified nasal polyp\n --PARENT--> [CA0J] Nasal polyp\n Def: Nasal polyp is an inflammatory and proliferating mass arising from the epithelial linings of nasal cavity and paranasal sinuses. In general, nasal polyp appears to be greyish white, smoothly surfaced,...\n --EXCLUDES--> [?] Benign neoplasm of middle ear, nasal cavity or accessory sinuses", "[DB71.Z] Anal polyp, unspecified\n --PARENT--> [DB71] Anal polyp\n Def: Abnormal mushroom-like growth sticking out from the epithelium rising from the lining of the anus and anal canal....\n --CHILD--> [DB71.0] Inflammatory anal polyp\n Def: Inflammatory polyp is an abnormal, mushroom-like growth sticking out from the mucous membrane that lines the anus. This mass is a reaction to some type of chronic inflammation in the anus....", "[DB71.Z] Anal polyp, unspecified\n --PARENT--> [DB71] Anal polyp\n Def: Abnormal mushroom-like growth sticking out from the epithelium rising from the lining of the anus and anal canal....\n --CHILD--> [DB71.1] Lymphoid polyp\n Def: Lymphoid polyp is a benign, focal or diffuse small polypoid lesion composed of well-differentiated lymphoid tissue....", "[DA09.0] Pulpitis\n Def: Inflammation of pulpal tissue resulting from irritating factors of diverse nature such as bacterial, hyperaemic, chemical or thermal that act directly or indirectly on the dental pulp....\n --PARENT--> [DA09] Diseases of pulp or periapical tissues\n Def: Dental pulp is that part of the tooth located in the centre of the coronal portion underneath dentin and composed of connective tissue, blood vessels and nerve endings.\nPeriapical tissues are designat...\n --CHILD--> [DA09.1] Necrosis of pulp\n Def: Necrosis of the dental pulp which clinically does not respond to thermal stimulation; the tooth may be asymptomatic or sensitive to percussion and palpation....", "[DA09.0] Pulpitis\n Def: Inflammation of pulpal tissue resulting from irritating factors of diverse nature such as bacterial, hyperaemic, chemical or thermal that act directly or indirectly on the dental pulp....\n --PARENT--> [DA09] Diseases of pulp or periapical tissues\n Def: Dental pulp is that part of the tooth located in the centre of the coronal portion underneath dentin and composed of connective tissue, blood vessels and nerve endings.\nPeriapical tissues are designat...\n --CHILD--> [DA09.1] Necrosis of pulp\n Def: Necrosis of the dental pulp which clinically does not respond to thermal stimulation; the tooth may be asymptomatic or sensitive to percussion and palpation...." ]
CA0J.Y
Other specified nasal polyp
[ { "from_icd11": "DB71.Z", "icd10_code": "K620", "icd10_title": "Anal polyp" }, { "from_icd11": "DA09.0", "icd10_code": "K0402", "icd10_title": "Irreversible pulpitis" }, { "from_icd11": "DA09.0", "icd10_code": "K0401", "icd10_title": "Reversible pulpitis" }, { "from_icd11": "DA09.0", "icd10_code": "K040", "icd10_title": "Pulpitis" }, { "from_icd11": "DE2Z", "icd10_code": "K5660", "icd10_title": "Unspecified intestinal obstruction" }, { "from_icd11": "DE2Z", "icd10_code": "K5903", "icd10_title": "Drug induced constipation" }, { "from_icd11": "DE2Z", "icd10_code": "K56600", "icd10_title": "Partial intestinal obstruction, unspecified as to cause" }, { "from_icd11": "DE2Z", "icd10_code": "K5669", "icd10_title": "Other intestinal obstruction" }, { "from_icd11": "DE2Z", "icd10_code": "K6389", "icd10_title": "Other specified diseases of intestine" }, { "from_icd11": "DE2Z", "icd10_code": "K5641", "icd10_title": "Fecal impaction" }, { "from_icd11": "DE2Z", "icd10_code": "K6289", "icd10_title": "Other specified diseases of anus and rectum" }, { "from_icd11": "DE2Z", "icd10_code": "K5901", "icd10_title": "Slow transit constipation" }, { "from_icd11": "DE2Z", "icd10_code": "K5650", "icd10_title": "Intestinal adhesions [bands], unspecified as to partial versus complete obstruction" }, { "from_icd11": "DE2Z", "icd10_code": "K56609", "icd10_title": "Unspecified intestinal obstruction, unspecified as to partial versus complete obstruction" }, { "from_icd11": "DE2Z", "icd10_code": "K5289", "icd10_title": "Other specified noninfective gastroenteritis and colitis" } ]
K620
Anal polyp
The masses seen at laparoscopy had the low power appearance of a well-differentiated carcinoma that was arranged primarily in solid nests. The tumor invaded through the muscularis propria and into the subserosal soft tissue . Multiple foci of tumor, the largest measuring three centimeters, were present in the lamina propria and submucosa as well as at the proximal and distal margins of resection. The tumor was composed of cells with abundant eosinophilic cytoplasm and round nuclei that contained finely stippled chromatin . Focal, mild anisokaryosis was present, but no necrosis was identified. The morphologic features were highly suspicious of a neuroendocrine tumor, so immunoperoxidase studies were performed for confirmation as well as ruling out an adenocarcinoma ( Table 1 ). The tumor was strongly and diffusely positive for synaptophysin and chromogranin, confirming neuroendocrine differentiation. To determine the grade of the tumor, a mitotic count and a Ki67 immunostain were also performed. The tumor had one mitosis per ten high power fields averaged over 50 high power fields, consistent with a G1. The Ki67 proliferation index was 3.5%, consistent with a G2. Since the proliferation index was of a higher grade, the tumor was graded as a G2. The tumor had metastasized to four lymph nodes , which, along with the tumor size and extent of invasion, was consistent with a more aggressive neoplasm.
4.242188
0.489746
sec[3]/p[0]
en
0.999997
25525544
https://doi.org/10.1155/2014/426161
[ "tumor", "power", "well", "consistent", "that", "propria", "present", "neuroendocrine", "grade", "fields" ]
[ { "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": "PB6Y", "title": "Other unintentional cause of morbidity or mortality" }, { "code": "PA83.2&XE02T", "title": "Accidental contact with powered knife" }, { "code": "MA80.1", "title": "Dysphasia" }, { "code": "PA83.2", "title": "Unintentionally cut or pierced by other or unspecified sharp object" }, { "code": "PA83.2&XE8MJ", "title": "Accidental contact with powered chain-saw" } ]
=== 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 [PB6Y] Other unintentional cause of morbidity or mortality Also known as: Other unintentional cause of morbidity or mortality | Exposure to other and unspecified man-made environmental factors | Exposure to other specified factors | Contact with agricultural machinery | contact with animal-powered farm machine [MA80.1] Dysphasia Definition: A cognitive disorder marked by an impaired ability to comprehend or express language in its written or spoken form. This condition is caused by diseases which affect the language areas of the dominant hemisphere. Clinical features are used to classify the various subtypes of this condition. Also known as: Dysphasia | loss of power of expression or comprehension | Alalia | Aphemia | Semantic dysphasia Excludes: progressive isolated aphasia | Developmental speech or language disorders [PA83.2] Unintentionally cut or pierced by other or unspecified sharp object Also known as: Unintentionally cut or pierced by other or unspecified sharp object | Unintentionally cut or pierced by archery objects | Contact with nonpowered hand tool | Accidental contact with axe | Accidental contact with can-opener === 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 --PARENT--> [02] Neoplasms Def: An abnormal or uncontrolled cellular proliferation which is not coordinated with an organism's requirements for normal tissue growth, replacement or repair.... --- Walk 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--> [2E61] Carcinoma in situ of other or unspecified digestive organs --- Walk 6 --- [2E6Z] Carcinoma in situ of unspecified site --PARENT--> [?] In situ neoplasms, except of lymphoid, haematopoietic, central nervous system or related tissues --CHILD--> [2E62] Carcinoma in situ of middle ear or respiratory system
[ "[2F9Z] Neoplasms of unknown behaviour of unspecified site\n --PARENT--> [?] Neoplasms of unknown behaviour, except of lymphoid, haematopoietic, central nervous system or related tissues\n --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 --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....", "[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--> [2E61] Carcinoma in situ of other or unspecified digestive organs", "[2E6Z] Carcinoma in situ of unspecified site\n --PARENT--> [?] In situ neoplasms, except of lymphoid, haematopoietic, central nervous system or related tissues\n --CHILD--> [2E62] Carcinoma in situ of middle ear or respiratory system" ]
2F9Z
Neoplasms of unknown behaviour of unspecified site
[ { "from_icd11": "2F9Z", "icd10_code": "D487", "icd10_title": "Neoplasm of uncertain behavior of other specified sites" }, { "from_icd11": "2F9Z", "icd10_code": "D482", "icd10_title": "Neoplasm of uncertain behavior of peripheral nerves and autonomic nervous system" }, { "from_icd11": "2F9Z", "icd10_code": "D37-D48", "icd10_title": "" }, { "from_icd11": "2F9Z", "icd10_code": "D377", "icd10_title": "" }, { "from_icd11": "2F9Z", "icd10_code": "D48", "icd10_title": "Neoplasm of uncertain behavior of other and unspecified sites" }, { "from_icd11": "2F9Z", "icd10_code": "D489", "icd10_title": "Neoplasm of uncertain behavior, unspecified" }, { "from_icd11": "ME61", "icd10_code": "R2240", "icd10_title": "Localized swelling, mass and lump, unspecified lower limb" }, { "from_icd11": "ME61", "icd10_code": "R2232", "icd10_title": "Localized swelling, mass and lump, left upper limb" }, { "from_icd11": "ME61", "icd10_code": "R2242", "icd10_title": "Localized swelling, mass and lump, left lower limb" }, { "from_icd11": "ME61", "icd10_code": "R2231", "icd10_title": "Localized swelling, mass and lump, right upper limb" }, { "from_icd11": "ME61", "icd10_code": "R2241", "icd10_title": "Localized swelling, mass and lump, right lower limb" }, { "from_icd11": "ME61", "icd10_code": "R2233", "icd10_title": "Localized swelling, mass and lump, upper limb, bilateral" }, { "from_icd11": "ME61", "icd10_code": "R2243", "icd10_title": "Localized swelling, mass and lump, lower limb, bilateral" }, { "from_icd11": "ME61", "icd10_code": "R2230", "icd10_title": "Localized swelling, mass and lump, unspecified upper limb" }, { "from_icd11": "ME61", "icd10_code": "R220", "icd10_title": "Localized swelling, mass and lump, head" } ]
D487
Neoplasm of uncertain behavior of other specified sites
In the presented case, the patient complained of postprandial abdominal pain after starting peritoneal dialysis. Intestinal TAO has been rarely reported. Kobayashi et al . reported a case of TAO with intestinal ischemia and reviewed the literature. They summarized 26 cases of visceral TAO including their case. The mean age of patients was 39.1, and all but two patients were male. The predominant symptom was abdominal pain, and 20 of 26 patients underwent digestive organ resection. The perioperative mortality rate was 30%, and only three patients underwent conservative treatment. The present patient experienced improvement in postprandial abdominal pain after avoiding dehydration and switching from peritoneal dialysis to hemodialysis. It is known that hemodialysis is more susceptible to intestinal ischemia than peritoneal dialysis because of its more unstable hemodynamics . The patient in this case underwent peritoneal dialysis for this reason; however, even though he was not dehydrated and his blood pressure was not low while receiving peritoneal dialysis, he experienced severe abdominal pain that got worse after starting peritoneal dialysis. His pain was relieved after stopping peritoneal dialysis. We presumed that hyperglycemia of the peritoneal cavity induced several changes, including leukostasis, vasoconstriction, and a pro-inflammatory state that caused aggravation of intestinal hypoxia .
4.109375
0.812988
sec[2]/p[3]
en
0.999997
26286269
https://doi.org/10.1186/s13256-015-0659-8
[ "peritoneal", "dialysis", "pain", "abdominal", "intestinal", "patients", "that", "postprandial", "starting", "ischemia" ]
[ { "code": "DC5Z", "title": "Diseases of peritoneum, unspecified" }, { "code": "DC50.Z", "title": "Peritonitis, unspecified" }, { "code": "NB91.Y&XA0KZ0", "title": "Peritoneal laceration" }, { "code": "2F94", "title": "Neoplasms of unknown behaviour of peritoneum" }, { "code": "DC51.Y", "title": "Other specified disorders of peritoneum or retroperitoneum" }, { "code": "QB94.Z", "title": "Care involving dialysis, unspecified" }, { "code": "QB94.1", "title": "Care involving extracorporeal dialysis" }, { "code": "9B73.0", "title": "Retinal detachment with retinal break" }, { "code": "QB94.2", "title": "Care involving peritoneal dialysis" }, { "code": "QB94.Y", "title": "Care involving other specified dialysis" } ]
=== ICD-11 CODES FOUND === [DC5Z] Diseases of peritoneum, unspecified Also known as: Diseases of peritoneum, unspecified | peritoneal disease [DC50.Z] Peritonitis, unspecified Also known as: Peritonitis, unspecified | Peritonitis | peritoneum inflammation | peritonitis of undetermined cause | peritonitis of unspecified cause [2F94] Neoplasms of unknown behaviour of peritoneum Also known as: Neoplasms of unknown behaviour of peritoneum | peritoneum tumour NOS [DC51.Y] Other specified disorders of peritoneum or retroperitoneum Also known as: Other specified disorders of peritoneum or retroperitoneum | Abdominal granuloma | Peritoneal granuloma | Epiploic appendagitis | Male frozen pelvis [QB94.Z] Care involving dialysis, unspecified Also known as: Care involving dialysis, unspecified | Care involving dialysis | dialysis preparation and treatment | dialysis NOS [QB94.1] Care involving extracorporeal dialysis Also known as: Care involving extracorporeal dialysis | encounter for extracorporeal dialysis | encounter for dialysis NOS | encounter for renal dialysis NOS | aftercare involving extracorporeal dialysis [9B73.0] Retinal detachment with retinal break Also known as: Retinal detachment with retinal break | Rhegmatogenous retinal detachment | ruptured retina with detachment | retinal hole with detachment | Retinal detachment with giant retinal tear Includes: Rhegmatogenous retinal detachment [QB94.2] Care involving peritoneal dialysis Also known as: Care involving peritoneal dialysis | aftercare involving peritoneal dialysis | intermittent peritoneal dialysis | peritoneum dialysis [QB94.Y] Care involving other specified dialysis Also known as: Care involving other specified dialysis === GRAPH WALKS === --- Walk 1 --- [DC5Z] Diseases of peritoneum, unspecified --PARENT--> [?] Diseases of peritoneum Def: This is the serous membrane that forms the lining of the abdominal cavity or the coelom—it covers most of the intra-abdominal (or coelomic) organs—in amniotes and some invertebrates.... --CHILD--> [?] Neoplasms of peritoneum or retroperitoneum Def: Neoplasms of peritoneum and retroperitoneum are the tumour originated from the peritoneum and the structure of the retroperitoneum. The tumour cells are derived from the mesothelium cells, nerve cells... --- Walk 2 --- [DC5Z] Diseases of peritoneum, unspecified --PARENT--> [?] Diseases of peritoneum Def: This is the serous membrane that forms the lining of the abdominal cavity or the coelom—it covers most of the intra-abdominal (or coelomic) organs—in amniotes and some invertebrates.... --PARENT--> [13] Diseases of the digestive system --- Walk 3 --- [DC50.Z] Peritonitis, unspecified --PARENT--> [DC50] Peritonitis Def: Peritonitis is inflammation of the peritoneum, a condition marked by exudations in the peritoneum of serum, fibrin, cells, and pus.... --EXCLUDES--> [?] Puerperal sepsis --- Walk 4 --- [DC50.Z] Peritonitis, unspecified --PARENT--> [DC50] Peritonitis Def: Peritonitis is inflammation of the peritoneum, a condition marked by exudations in the peritoneum of serum, fibrin, cells, and pus.... --EXCLUDES--> [?] Genital tract or pelvic infection following abortion, ectopic or molar pregnancy --- Walk 5 --- [2F94] Neoplasms of unknown behaviour of peritoneum --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 6 --- [2F94] Neoplasms of unknown behaviour of peritoneum --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
[ "[DC5Z] Diseases of peritoneum, unspecified\n --PARENT--> [?] Diseases of peritoneum\n Def: This is the serous membrane that forms the lining of the abdominal cavity or the coelom—it covers most of the intra-abdominal (or coelomic) organs—in amniotes and some invertebrates....\n --CHILD--> [?] Neoplasms of peritoneum or retroperitoneum\n Def: Neoplasms of peritoneum and retroperitoneum are the tumour originated from the peritoneum and the structure of the retroperitoneum. The tumour cells are derived from the mesothelium cells, nerve cells...", "[DC5Z] Diseases of peritoneum, unspecified\n --PARENT--> [?] Diseases of peritoneum\n Def: This is the serous membrane that forms the lining of the abdominal cavity or the coelom—it covers most of the intra-abdominal (or coelomic) organs—in amniotes and some invertebrates....\n --PARENT--> [13] Diseases of the digestive system", "[DC50.Z] Peritonitis, unspecified\n --PARENT--> [DC50] Peritonitis\n Def: Peritonitis is inflammation of the peritoneum, a condition marked by exudations in the peritoneum of serum, fibrin, cells, and pus....\n --EXCLUDES--> [?] Puerperal sepsis", "[DC50.Z] Peritonitis, unspecified\n --PARENT--> [DC50] Peritonitis\n Def: Peritonitis is inflammation of the peritoneum, a condition marked by exudations in the peritoneum of serum, fibrin, cells, and pus....\n --EXCLUDES--> [?] Genital tract or pelvic infection following abortion, ectopic or molar pregnancy", "[2F94] Neoplasms of unknown behaviour of peritoneum\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", "[2F94] Neoplasms of unknown behaviour of peritoneum\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" ]
DC5Z
Diseases of peritoneum, unspecified
[ { "from_icd11": "DC5Z", "icd10_code": "K67", "icd10_title": "Disorders of peritoneum in infectious diseases classified elsewhere" }, { "from_icd11": "DC5Z", "icd10_code": "K65-K67", "icd10_title": "" }, { "from_icd11": "DC50.Z", "icd10_code": "K651", "icd10_title": "Peritoneal abscess" }, { "from_icd11": "DC50.Z", "icd10_code": "K652", "icd10_title": "Spontaneous bacterial peritonitis" }, { "from_icd11": "DC50.Z", "icd10_code": "K654", "icd10_title": "Sclerosing mesenteritis" }, { "from_icd11": "DC50.Z", "icd10_code": "K653", "icd10_title": "Choleperitonitis" }, { "from_icd11": "DC50.Z", "icd10_code": "K659", "icd10_title": "Peritonitis, unspecified" }, { "from_icd11": "DC50.Z", "icd10_code": "K658", "icd10_title": "Other peritonitis" }, { "from_icd11": "DC50.Z", "icd10_code": "K650", "icd10_title": "Generalized (acute) peritonitis" }, { "from_icd11": "DC50.Z", "icd10_code": "K65", "icd10_title": "Peritonitis" }, { "from_icd11": "2F94", "icd10_code": "D484", "icd10_title": "Neoplasm of uncertain behavior of peritoneum" }, { "from_icd11": "QB94.Z", "icd10_code": "Z4931", "icd10_title": "Encounter for adequacy testing for hemodialysis" }, { "from_icd11": "QB94.Z", "icd10_code": "Z4932", "icd10_title": "Encounter for adequacy testing for peritoneal dialysis" }, { "from_icd11": "QB94.Z", "icd10_code": "Z49", "icd10_title": "Encounter for care involving renal dialysis" }, { "from_icd11": "QB94.1", "icd10_code": "Z491", "icd10_title": "" } ]
K67
Disorders of peritoneum in infectious diseases classified elsewhere
Failure to respond to appropriate antibiotics should prompt a broader differential diagnosis beyond bacterial infection in cases of persistent dermatologic lesions. Cutaneous blastomycosis specifically should be suspected in patients with frequent travel in the Midwestern United States, despite the absence of recent respiratory infections. Primary inoculation, although rare, should be considered in patients with significant history of outdoor activities. In our patient, the initial diagnosis was hinged on a bacterial infection with Enterococcus faecalis . The patient’s travel history could have prompted an earlier investigation into fungal etiologies. However, it was not until the patient failed to respond to antibiotics that a biopsy and fungal cultures were sent, resulting in significant delay in treatment despite extensive spread of lesions. In order to prevent misdiagnosis and delays in treatment, fungal etiologies should be high on the differential; histopathologic specimen and fungal cultures should be sent at the outset for accurate diagnosis and treatment. In cases of fungal infection particularly blastomycosis, histology is key as it helps differentiate blastomycosis from various other infections and malignancies that have a similar presentation. Likewise, thorough exposure history and knowledge of other mimickers is just as important in prompt diagnosis and treatment of blastomycosis.
4.21875
0.644531
sec[3]/p[0]
en
0.999998
PMC8881278
https://doi.org/10.7759/cureus.21634
[ "fungal", "blastomycosis", "infection", "respond", "antibiotics", "prompt", "differential", "bacterial", "cases", "lesions" ]
[ { "code": "9A71&XN8AY", "title": "Fungal keratitis" }, { "code": "DA25.11", "title": "Fungal oesophageal ulcer" }, { "code": "DA60.7&XN8AY", "title": "Fungal gastric ulcer" }, { "code": "DA63.62", "title": "Fungal duodenal ulcer" }, { "code": "FA10.2", "title": "Fungal infection of joint" }, { "code": "1F22", "title": "Blastomycosis" }, { "code": "1F27.Z", "title": "Cryptococcosis, unspecified" }, { "code": "1F2E.Z", "title": "Paracoccidioidomycosis, unspecified" }, { "code": "1F2E.0", "title": "Pulmonary paracoccidioidomycosis" }, { "code": "1F2E.Y", "title": "Other specified paracoccidioidomycosis" } ]
=== ICD-11 CODES FOUND === [DA25.11] Fungal oesophageal ulcer Definition: Ulcer in the mucosa of oesophagus due to fungal infection. Also known as: Fungal oesophageal ulcer [DA63.62] Fungal duodenal ulcer Definition: Duodenal ulcer caused by infection with fungus. This includes infection with candida and other fungal infections in the duodenum. Also known as: Fungal duodenal ulcer | Duodenal ulcer due to fungal infections [FA10.2] Fungal infection of joint Also known as: Fungal infection of joint | Arthritis in mycoses | Fungal infection of joint, multiple sites | arthritis in mycoses, multiple sites | Fungal infection of joint, shoulder region [1F22] Blastomycosis Definition: A disease caused by an infection with the fungi Blastomyces dermatitidis. This disease is characterised by fever, chills, cough, myalgia, arthralgia, or chest pain. This disease may also present in the skin and bones. Transmission is by inhalation of fungal spores. Confirmation is by identification of Blastomyces dermatitidis in a urine, cerebrospinal fluid, or blood sample. Also known as: Blastomycosis | North American blastomycosis | Gilchrist disease | Chicago disease or disorder | infection by blastomyces dermatitidis Excludes: Brazilian blastomycosis | keloidal blastomycosis [1F27.Z] Cryptococcosis, unspecified Also known as: Cryptococcosis, unspecified | Cryptococcosis | cryptococcosis infection | cryptococcus neoformans infection | European blastomycosis [1F2E.Z] Paracoccidioidomycosis, unspecified Also known as: Paracoccidioidomycosis, unspecified | Paracoccidioidomycosis | Brazilian blastomycosis | Lutz disease | Brazilian blastomycotic [1F2E.0] Pulmonary paracoccidioidomycosis Definition: A disease of the pulmonary system, caused by an infection with the fungi Paracoccidioides brasiliensis. This disease is characterised by fever, cough, dyspnoea, or malaise. Transmission is by inhalation of fungal spores. Confirmation is by identification of Paracoccidioides brasiliensis in a blood or sputum sample. Also known as: Pulmonary paracoccidioidomycosis | pulmonary south american blastomycosis [1F2E.Y] Other specified paracoccidioidomycosis Also known as: Other specified paracoccidioidomycosis | Extrapulmonary paracoccidioidomycosis | south american visceral blastomycosis | visceral paracoccidioidomycosis | Mucocutaneous paracoccidioidomycosis === GRAPH WALKS === --- Walk 1 --- [DA25.11] Fungal oesophageal ulcer Def: Ulcer in the mucosa of oesophagus due to fungal infection.... --PARENT--> [DA25.1] Infectious oesophageal ulcer Def: Infectious oesophageal ulcer is ulceration or erosion in the mucosa of oesophagus due to the infectious agent, such as bacteria, viruses, fungi and parasites.... --CHILD--> [DA25.12] Parasitic oesophageal ulcer Def: Ulcer in the mucosa of oesophagus due to parasitic infection.... --- Walk 2 --- [DA25.11] Fungal oesophageal ulcer Def: Ulcer in the mucosa of oesophagus due to fungal infection.... --PARENT--> [DA25.1] Infectious oesophageal ulcer Def: Infectious oesophageal ulcer is ulceration or erosion in the mucosa of oesophagus due to the infectious agent, such as bacteria, viruses, fungi and parasites.... --CHILD--> [DA25.12] Parasitic oesophageal ulcer Def: Ulcer in the mucosa of oesophagus due to parasitic infection.... --- Walk 3 --- [DA63.62] Fungal duodenal ulcer Def: Duodenal ulcer caused by infection with fungus. This includes infection with candida and other fungal infections in the duodenum.... --PARENT--> [DA63.6] Infectious duodenal ulcer --CHILD--> [DA63.62] Fungal duodenal ulcer Def: Duodenal ulcer caused by infection with fungus. This includes infection with candida and other fungal infections in the duodenum.... --- Walk 4 --- [DA63.62] Fungal duodenal ulcer Def: Duodenal ulcer caused by infection with fungus. This includes infection with candida and other fungal infections in the duodenum.... --PARENT--> [DA63.6] Infectious duodenal ulcer --CHILD--> [DA63.62] Fungal duodenal ulcer Def: Duodenal ulcer caused by infection with fungus. This includes infection with candida and other fungal infections in the duodenum.... --- Walk 5 --- [FA10.2] Fungal infection of joint --PARENT--> [FA10] Direct infections of joint Def: Hematogenic or non-hematogenic infections of joints.... --PARENT--> [?] 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 6 --- [FA10.2] Fungal infection of joint --PARENT--> [FA10] Direct infections of joint Def: Hematogenic or non-hematogenic infections of joints.... --EXCLUDES--> [?] Reactive arthropathies Def: A disease of the joints, caused by an infection in another part of the body, auto-immune disease, or post-vaccination. This disease is characterised by a secondary inflammation of the joints in reacti...
[ "[DA25.11] Fungal oesophageal ulcer\n Def: Ulcer in the mucosa of oesophagus due to fungal infection....\n --PARENT--> [DA25.1] Infectious oesophageal ulcer\n Def: Infectious oesophageal ulcer is ulceration or erosion in the mucosa of oesophagus due to the infectious agent, such as bacteria, viruses, fungi and parasites....\n --CHILD--> [DA25.12] Parasitic oesophageal ulcer\n Def: Ulcer in the mucosa of oesophagus due to parasitic infection....", "[DA25.11] Fungal oesophageal ulcer\n Def: Ulcer in the mucosa of oesophagus due to fungal infection....\n --PARENT--> [DA25.1] Infectious oesophageal ulcer\n Def: Infectious oesophageal ulcer is ulceration or erosion in the mucosa of oesophagus due to the infectious agent, such as bacteria, viruses, fungi and parasites....\n --CHILD--> [DA25.12] Parasitic oesophageal ulcer\n Def: Ulcer in the mucosa of oesophagus due to parasitic infection....", "[DA63.62] Fungal duodenal ulcer\n Def: Duodenal ulcer caused by infection with fungus. This includes infection with candida and other fungal infections in the duodenum....\n --PARENT--> [DA63.6] Infectious duodenal ulcer\n --CHILD--> [DA63.62] Fungal duodenal ulcer\n Def: Duodenal ulcer caused by infection with fungus. This includes infection with candida and other fungal infections in the duodenum....", "[DA63.62] Fungal duodenal ulcer\n Def: Duodenal ulcer caused by infection with fungus. This includes infection with candida and other fungal infections in the duodenum....\n --PARENT--> [DA63.6] Infectious duodenal ulcer\n --CHILD--> [DA63.62] Fungal duodenal ulcer\n Def: Duodenal ulcer caused by infection with fungus. This includes infection with candida and other fungal infections in the duodenum....", "[FA10.2] Fungal infection of joint\n --PARENT--> [FA10] Direct infections of joint\n Def: Hematogenic or non-hematogenic infections of joints....\n --PARENT--> [?] 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 ...", "[FA10.2] Fungal infection of joint\n --PARENT--> [FA10] Direct infections of joint\n Def: Hematogenic or non-hematogenic infections of joints....\n --EXCLUDES--> [?] Reactive arthropathies\n Def: A disease of the joints, caused by an infection in another part of the body, auto-immune disease, or post-vaccination. This disease is characterised by a secondary inflammation of the joints in reacti..." ]
9A71&XN8AY
Fungal keratitis
[ { "from_icd11": "FA10.2", "icd10_code": "M016", "icd10_title": "" }, { "from_icd11": "1F22", "icd10_code": "B403", "icd10_title": "Cutaneous blastomycosis" }, { "from_icd11": "1F22", "icd10_code": "B400", "icd10_title": "Acute pulmonary blastomycosis" }, { "from_icd11": "1F22", "icd10_code": "B409", "icd10_title": "Blastomycosis, unspecified" }, { "from_icd11": "1F22", "icd10_code": "B40", "icd10_title": "Blastomycosis" }, { "from_icd11": "1F22", "icd10_code": "B401", "icd10_title": "Chronic pulmonary blastomycosis" }, { "from_icd11": "1F22", "icd10_code": "B402", "icd10_title": "Pulmonary blastomycosis, unspecified" }, { "from_icd11": "1F22", "icd10_code": "B407", "icd10_title": "Disseminated blastomycosis" }, { "from_icd11": "1F22", "icd10_code": "B408", "icd10_title": "Other forms of blastomycosis" }, { "from_icd11": "1F27.Z", "icd10_code": "B459", "icd10_title": "Cryptococcosis, unspecified" }, { "from_icd11": "1F27.Z", "icd10_code": "B458", "icd10_title": "Other forms of cryptococcosis" }, { "from_icd11": "1F27.Z", "icd10_code": "B45", "icd10_title": "Cryptococcosis" }, { "from_icd11": "1F27.Z", "icd10_code": "B452", "icd10_title": "Cutaneous cryptococcosis" }, { "from_icd11": "1F27.Z", "icd10_code": "B453", "icd10_title": "Osseous cryptococcosis" }, { "from_icd11": "1F2E.Z", "icd10_code": "B419", "icd10_title": "Paracoccidioidomycosis, unspecified" } ]
M016
Discussion of the clinical case : The patient has metabolic, cardiorespiratory, and muscular alterations . Previous management was limited to a pharmacological approach, without considering lifestyle changes, such as nutritional and physical activity modifications. Basic evaluations were lacking at the time of patient admission to the cardiometabolic risk program, such as body composition, VO 2max , grip strength, and gait speed. An adequate follow-up and an early intervention would have improved the health of the patient before. Fig. 2 General evolution of cardiorespiratory fitness and muscle status during lifetime. Both conditions rapidly increase during youth, then stabilize during early adulthood, and finally decrease with slow, more or less linear kinetics. There is always variability in the values found across all ages, from which those in the lowest quartile (below percentile 25th, P25, i.e., below the white, discontinuous line) are at increased risk of cardiometabolic morbidity and mortality. The white dot illustrates the position of the patient in the clinical case regarding the distribution of the population of the same age. The routine evaluation of cardiorespiratory fitness and muscle status in adults allows to identify those below the P25 and take effective actions to help them soon cross the line over the P25 (white arrow in the insert), notably reducing their cardiometabolic risk
4.027344
0.911133
sec[5]/p[9]
en
0.999996
36683091
https://doi.org/10.1007/s00421-022-05114-y
[ "cardiorespiratory", "cardiometabolic", "risk", "white", "fitness", "muscle", "status", "those", "line", "discussion" ]
[ { "code": "MC82.4", "title": "Cardiopulmonary arrest" }, { "code": "CB00", "title": "Acute respiratory distress syndrome" }, { "code": "MG40.0", "title": "Cardiogenic shock" }, { "code": "BA01/BD1Z", "title": "Hypertensive heart disease with heart failure" }, { "code": "KB23.0Z", "title": "Respiratory distress syndrome of newborn, unspecified" }, { "code": "5D0Y", "title": "Other specified metabolic disorders" }, { "code": "BC43.10", "title": "Familial-genetic hypertrophic cardiomyopathy" }, { "code": "QC4Y", "title": "Personal history of other specified health problems" }, { "code": "QA43.Z", "title": "Supervision of high-risk pregnancy, unspecified" }, { "code": "QA43.Y", "title": "Other specified supervision of high-risk pregnancy" } ]
=== ICD-11 CODES FOUND === [MC82.4] Cardiopulmonary arrest Also known as: Cardiopulmonary arrest | cardiopulmonary collapse | cardiorespiratory arrest | acute cardiopulmonary arrest | cardiopulmonary failure [CB00] Acute respiratory distress syndrome Definition: 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 hypoxic respiratory failure caused by intense pulmonary inflammation that develops after a severe physiologic insult. Also known as: Acute respiratory distress syndrome | Adult acute respiratory distress syndrome | Adult hyaline membrane disease | acquired respiratory distress syndrome | congestive atelectasis [MG40.0] Cardiogenic shock Also known as: Cardiogenic shock | cardiorespiratory collapse | acute myocardial shock | acute cardiogenic shock NOS | cardiogenic shock NOS Excludes: Cardiogenic shock, unrelated to mechanical complications, as current complication following acute myocardial infarction [KB23.0Z] Respiratory distress syndrome of newborn, unspecified Also known as: Respiratory distress syndrome of newborn, unspecified | Respiratory distress syndrome of newborn | cardiorespiratory distress syndrome of newborn | distress respiratory syndrome newborn | idiopathic respiratory distress syndrome [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 [BC43.10] Familial-genetic hypertrophic cardiomyopathy Definition: Familial isolated hypertrophic cardiomyopathy is the presence of non-syndromic hypertrophic cardiomyopathy in multiple members of a pedigree, or in the presence of a genetic mutation known to be significantly associated with hypertrophic cardiomyopathy. Also known as: Familial-genetic hypertrophic cardiomyopathy | Familial hypertrophic cardiomyopathy | Hereditary ventricular hypertrophy | Hypertrophic cardiomyopathy due to disorder of fatty acid metabolism | Fatty acid oxidation or ketogenesis disorder with hypertrophic cardiomyopathy [QC4Y] Personal history of other specified health problems Also known as: Personal history of other specified health problems | Personal history of diseases of the circulatory system | history of disease or disorder of circulatory system | personal history of conditions classifiable as diseases of the circulatory system | Personal history of diseases of the respiratory system [QA43.Z] Supervision of high-risk pregnancy, unspecified Also known as: Supervision of high-risk pregnancy, unspecified | Supervision of high-risk pregnancy [QA43.Y] Other specified supervision of high-risk pregnancy Also known as: Other specified supervision of high-risk pregnancy | Supervision of pregnancy with grand multiparity | pregnancy management affected by grand multiparity | multiparity affecting management of pregnancy, labour and delivery | pregnancy supervision for multiparity === GRAPH WALKS === --- Walk 1 --- [MC82.4] Cardiopulmonary arrest --PARENT--> [MC82] Cardiac arrest Def: A sudden, sometimes temporary, cessation of heart function resulting in hemodynamic collapse.... --CHILD--> [MC82.2] Asystolic cardiac arrest Def: Absence of electrical activity of the heart resulting in hemodynamic collapse.... --- Walk 2 --- [MC82.4] Cardiopulmonary arrest --PARENT--> [MC82] Cardiac arrest Def: A sudden, sometimes temporary, cessation of heart function resulting in hemodynamic collapse.... --CHILD--> [MC82.2] Asystolic cardiac arrest Def: Absence of electrical activity of the heart resulting in hemodynamic collapse.... --- Walk 3 --- [CB00] 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... --RELATED_TO--> [?] Respiratory distress syndrome of newborn Def: Respiratory distress syndrome (RDS) is an acute illness, usually of preterm infants, due to pulmonary surfactant deficiency, developing within 4-6 hours of birth, and is characterised by respiratory d... --PARENT--> [?] Respiratory distress of newborn Def: A condition characterised by developmental insufficiency of surfactant associated proteins or surfactant production and structural immaturity in the lungs.... --- Walk 4 --- [CB00] 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... --RELATED_TO--> [?] Respiratory distress syndrome of newborn Def: Respiratory distress syndrome (RDS) is an acute illness, usually of preterm infants, due to pulmonary surfactant deficiency, developing within 4-6 hours of birth, and is characterised by respiratory d... --CHILD--> [?] Respiratory distress syndrome of the newborn, altered by maternal corticosteroid therapy --- Walk 5 --- [MG40.0] Cardiogenic shock --EXCLUDES--> [?] Cardiogenic shock, unrelated to mechanical complications, as current complication following acute myocardial infarction Def: The most severe clinical expression of left ventricular failure and is associated with extensive damage to the left ventricular myocardium after acute myocardial infarction, unrelated to a mechanical ... --PARENT--> [?] Certain current complications following acute myocardial infarction Def: Secondary conditions which may occur in the course after the heart attack. They include pericarditis, arrhythmia, cardiogenic shock, heart failure, ventricular rupture, ventricular aneurysm (with thro... --- Walk 6 --- [MG40.0] Cardiogenic shock --EXCLUDES--> [?] Cardiogenic shock, unrelated to mechanical complications, as current complication following acute myocardial infarction Def: The most severe clinical expression of left ventricular failure and is associated with extensive damage to the left ventricular myocardium after acute myocardial infarction, unrelated to a mechanical ... --PARENT--> [?] Certain current complications following acute myocardial infarction Def: Secondary conditions which may occur in the course after the heart attack. They include pericarditis, arrhythmia, cardiogenic shock, heart failure, ventricular rupture, ventricular aneurysm (with thro...
[ "[MC82.4] Cardiopulmonary arrest\n --PARENT--> [MC82] Cardiac arrest\n Def: A sudden, sometimes temporary, cessation of heart function resulting in hemodynamic collapse....\n --CHILD--> [MC82.2] Asystolic cardiac arrest\n Def: Absence of electrical activity of the heart resulting in hemodynamic collapse....", "[MC82.4] Cardiopulmonary arrest\n --PARENT--> [MC82] Cardiac arrest\n Def: A sudden, sometimes temporary, cessation of heart function resulting in hemodynamic collapse....\n --CHILD--> [MC82.2] Asystolic cardiac arrest\n Def: Absence of electrical activity of the heart resulting in hemodynamic collapse....", "[CB00] 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 --RELATED_TO--> [?] Respiratory distress syndrome of newborn\n Def: Respiratory distress syndrome (RDS) is an acute illness, usually of preterm infants, due to pulmonary surfactant deficiency, developing within 4-6 hours of birth, and is characterised by respiratory d...\n --PARENT--> [?] Respiratory distress of newborn\n Def: A condition characterised by developmental insufficiency of surfactant associated proteins or surfactant production and structural immaturity in the lungs....", "[CB00] 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 --RELATED_TO--> [?] Respiratory distress syndrome of newborn\n Def: Respiratory distress syndrome (RDS) is an acute illness, usually of preterm infants, due to pulmonary surfactant deficiency, developing within 4-6 hours of birth, and is characterised by respiratory d...\n --CHILD--> [?] Respiratory distress syndrome of the newborn, altered by maternal corticosteroid therapy", "[MG40.0] Cardiogenic shock\n --EXCLUDES--> [?] Cardiogenic shock, unrelated to mechanical complications, as current complication following acute myocardial infarction\n Def: The most severe clinical expression of left ventricular failure and is associated with extensive damage to the left ventricular myocardium after acute myocardial infarction, unrelated to a mechanical ...\n --PARENT--> [?] Certain current complications following acute myocardial infarction\n Def: Secondary conditions which may occur in the course after the heart attack. They include pericarditis, arrhythmia, cardiogenic shock, heart failure, ventricular rupture, ventricular aneurysm (with thro...", "[MG40.0] Cardiogenic shock\n --EXCLUDES--> [?] Cardiogenic shock, unrelated to mechanical complications, as current complication following acute myocardial infarction\n Def: The most severe clinical expression of left ventricular failure and is associated with extensive damage to the left ventricular myocardium after acute myocardial infarction, unrelated to a mechanical ...\n --PARENT--> [?] Certain current complications following acute myocardial infarction\n Def: Secondary conditions which may occur in the course after the heart attack. They include pericarditis, arrhythmia, cardiogenic shock, heart failure, ventricular rupture, ventricular aneurysm (with thro..." ]
MC82.4
Cardiopulmonary arrest
[ { "from_icd11": "CB00", "icd10_code": "J80", "icd10_title": "Acute respiratory distress syndrome" }, { "from_icd11": "MG40.0", "icd10_code": "R570", "icd10_title": "Cardiogenic shock" }, { "from_icd11": "BA01/BD1Z", "icd10_code": "I110", "icd10_title": "Hypertensive heart disease with heart failure" }, { "from_icd11": "KB23.0Z", "icd10_code": "P220", "icd10_title": "Respiratory distress syndrome of newborn" }, { "from_icd11": "QC4Y", "icd10_code": "Z86718", "icd10_title": "Personal history of other venous thrombosis and embolism" }, { "from_icd11": "QC4Y", "icd10_code": "Z9181", "icd10_title": "History of falling" }, { "from_icd11": "QA43.Z", "icd10_code": "Z35", "icd10_title": "" }, { "from_icd11": "QA43.Z", "icd10_code": "Z354", "icd10_title": "" }, { "from_icd11": "QA43.Z", "icd10_code": "Z358", "icd10_title": "" }, { "from_icd11": "QA43.Z", "icd10_code": "Z359", "icd10_title": "" }, { "from_icd11": "QA43.Z", "icd10_code": "O0990 ", "icd10_title": "" }, { "from_icd11": "QA43.Z", "icd10_code": "O0993 ", "icd10_title": "" }, { "from_icd11": "QA43.Y", "icd10_code": "O09521 ", "icd10_title": "" }, { "from_icd11": "QA43.Y", "icd10_code": "O09522 ", "icd10_title": "" }, { "from_icd11": "QA43.Y", "icd10_code": "O09523 ", "icd10_title": "" } ]
J80
Acute respiratory distress syndrome