Miyano T, Suruga K, Tsuchiya H, Suda K
J Pediatr Surg. 1977 Feb;12(1):19-25. doi: 10.1016/0022-3468(77)90291-3.
Histopathological study of the remnant of extrahepatic bile ducts in 40 cases of so-called uncorrectable biliary atresia, upon which we operated the last three years, has been performed. The histological findings of the remnant were classified into three types. Only two cases were found to have type 1a ducts in the porta hepatis area, from which we can expect better prognosis postoperatively. We also found that as the patients become older, the size of the duct in the remnant becomes smaller and the hepatic fibrosis becomes more remarkable. Therefore the operation should be performed in the infant with this lesion as young as possible. As for the evaluation of operative results of hepatic portoenterostomy for this lesion, a proper evaluation can be made only in those cases in which a microscopic examination of the remnant of extrahepatic bile duct at the porta hepatis area has been adequately performed. Concerning the pathogenesis of biliary atresia, we presume that congenital abnormalities of bile ducts are a basic factor, and additional nonspecific inflammation and bile stasis complete its pathological condition.
对过去三年我们实施手术的40例所谓不可纠正性胆道闭锁患者肝外胆管残余组织进行了组织病理学研究。残余组织的组织学表现分为三种类型。仅发现两例肝门区存在1a型胆管,这类患者术后预后有望更好。我们还发现,随着患者年龄增长,残余胆管管径变细,肝纤维化更显著。因此,对于患有此病变的婴儿应尽早进行手术。对于该病变的肝门空肠吻合术手术效果评估,只有在对肝门区肝外胆管残余组织进行充分显微镜检查的病例中才能做出恰当评估。关于胆道闭锁的发病机制,我们推测胆管先天性异常是基本因素,额外的非特异性炎症和胆汁淤积使其病理状况得以完善。