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胆总管缺如

Agenesis of the common bile duct.

作者信息

Markle G B

出版信息

Arch Surg. 1981 Mar;116(3):350-2. doi: 10.1001/archsurg.1981.01380150068018.

Abstract

In a case of congenital absence of the common bile duct, the common hepatic duct emptied directly into the gallbladder; the latter drained by a long cystic duct into the second part of the duodenum. To my knowledge, only eight prior cases with this or very similar anomalies have been reported in the literature. This rare arrangement is common in certain lower animals and is explainable by embryologic studies. Cholecystectomy in these cases inevitably produces a complete defect in the biliary tract, which should be recognized and repaired primarily. Reconstruction using a modified Rodney Smith sutureless technique was successful, and apparently this is the first case where it has been used for this purpose.

摘要

在一例先天性胆总管缺如的病例中,肝总管直接汇入胆囊;胆囊通过一条长的胆囊管引流至十二指肠第二部。据我所知,文献中仅报道过8例具有这种或非常相似异常情况的病例。这种罕见的结构在某些低等动物中很常见,并且可以通过胚胎学研究来解释。在这些病例中进行胆囊切除术不可避免地会导致胆道出现完全缺损,应首先认识到这一点并进行修复。采用改良的罗德尼·史密斯无缝合技术进行重建获得了成功,显然这是首例将该技术用于此目的的病例。

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