肝外胆道闭锁及胆胰总管。关于一个案例的文献综述]。

Chirurgie pediatrique Pub Date : 1990-01-01
P Vergnes, T Lamireau, J R Pontailler, J F Colombani, J M Bondonny
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引用次数: 0

摘要

作者报告的情况下,一个3个月大的高加索男孩有肝外胆道闭锁与先天性胆道囊肿和异常胰胆道交界处。胆囊和十二指肠之间的通畅允许手术对这条长而常见的胰胆通道进行混浊。先天性胆道囊肿位于胆总管上部,因胆道结瘤而梗阻。不幸的是,没有发现肝内胆管和囊肿之间的通畅。由于这种长而常见的胰胆通道可能导致胆道扩张或胆道癌,我们采用肝门肠造口术而不是肝门胆囊造口术。几周后,胆汁流动恢复,黄疸减轻。经过18个月的随访,尽管手术活检发现肝纤维化,但该男孩目前无黄疸。肝外胆道闭锁合并胰胆总管较少见,仅报道20例。在本例中,胰液返流到胆道可能导致胆总管扩张和慢性梗阻性胆管病引起的胆道闭锁。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Extrahepatic biliary tract atresia and a common biliopancreatic canal. Review of the literature apropos of a case].

The authors report the case of an 3 months old caucasian boy which had an extrahepatic biliary atresia associate with a congenital biliary cyst and an anomalous pancreaticobiliary junction. The patency between gallbladder and duodenum permits the operative opacification of this long common pancreaticobiliary channel. The congenital biliary cyst was located on the upper part of the common bile duct and was obstructed by biliary concretions. Unfortunately, no patency between intrahepatic bile ducts and this cyst was found. Because this long common pancreaticobiliary channel may cause biliary dilatation or biliary cancer, we performed an hepatic portoenterostomy rather an hepatic portocholecystostomy. A few weeks later, the bile flow was restored and the jaundice decreased. With a follow up of 18 months, this boy is currently anicteric, despite the hepatic fibrosis found on the operative biopsy. The association extrahepatic biliary atresia-long common pancreaticobiliary channel is uncommon and only 20 cases were reported. In our case, the pancreatic juice reflux into the biliary tract might have caused the dilatation of the common bile duct and the biliary atresia by chronic obstructive cholangiopathy.

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