LB20.21
胆道闭锁
Biliary atresia
- 上级条目
- LB20.2 胆管结构发育异常
- 层级
- 6 级
定义
胆道闭锁是一种罕见疾病，其特点是在新生儿期出现不明原因的炎症性胆道梗阻。它是这个年龄组中胆汁淤积性黄疸最常见的外科原因。如果未经治疗，会导致肝硬化，并在出生后最初几年内死亡。
Biliary atresia is a rare disease characterised by an inflammatory biliary obstruction of unknown origin that presents in the neonatal period. It is the most frequent surgical cause of cholestatic jaundice in this age group. Untreated, this condition leads to cirrhosis and death within the first years of life.
索引词 可用于检索该条目的同义词与别名
- 胆道闭锁
- 胆管闭锁
- 先天性胆管闭锁
- 先天性胆道闭锁
- BA[胆道闭锁]
- 胆管不通
- 胆管闭锁
- 胆总管闭锁 [possible translation]
- 胆管闭锁 [possible translation]
- 胆管闭锁 [possible translation]
- 胆囊管闭锁 [possible translation]
- 胆管闭锁
- 胆管闭锁
- 胆囊管闭锁
- 胆总管闭锁
- 肝外胆道闭锁
- 先天性肝外胆管闭锁
- EHBA[肝外胆道闭锁]
- 肝内胆道闭锁
- 先天性肝管梗阻
英文词条（16）
- Biliary atresia
- Atresia of bile ducts
- BA - [biliary atresia]
- atresia of common duct
- bile duct atresia
- bile ductal atresia
- biliary duct atresia
- congenital bile duct atresia
- congenital biliary atresia
- cystic duct atresia
- impervious bile duct
- Extrahepatic biliary atresia
- EHBA - [extrahepatic biliary atresia]
- congenital atresia of extrahepatic bile duct
- Intrahepatic biliary atresia
- congenital hepatic ductal obstruction
后组配轴 Postcoordination
该条目未定义后组配轴，直接使用上面的编码即可。后组配是在主干编码之后追加侧别、具体解剖部位、严重程度、病因等细节的可选组合方式，不是必填项。