Sookpotarom P, Vejchapipat P
Department of Surgery, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.
Eur J Pediatr Surg. 2007 Aug;17(4):295-7. doi: 10.1055/s-2007-965537.
Biliary atresia constitutes a serious problem in early infancy, due to the concomitant cholestasis. The conventional classification falls into 3 main types: type I, atresia of the common bile duct; type II, atresia of the hepatic duct; and type III, atresia of the porta hepatis. We report 2 unusual cases of biliary atresia type III with a cystic structure that could be mistaken for correctable biliary atresia or choledochal cyst.
由于伴有胆汁淤积，胆道闭锁在婴儿早期是一个严重问题。传统分类主要分为3种类型：I型，胆总管闭锁；II型，肝管闭锁；III型，肝门部闭锁。我们报告2例不寻常的III型胆道闭锁病例，其具有囊性结构，可能被误诊为可矫正的胆道闭锁或胆总管囊肿。
