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Congenital Cystic Malformation of the Bile Ducts

机译:胆管先天性囊性畸形

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摘要

A 20-year-old woman had a cyst of the proximal part of the common bile duct and a cyst of the left hepatic duct; these lesions were diagnosed preoperatively by intravenous cholangiography and successfully operated upon. At the time of writing, she has been followed up for one year.Congenital defects in the biliary system are rare and, in a review of the literature, only two cases were found similar to this one. It is generally accepted that these lesions are congenital, but the exact pathogenesis is unknown.Alonso-Lej, Rever and Pessagno2 reviewed the literature in 1959 and found 403 authentic congenital cysts of the hepatic ducts. The most common congenital defect is a single choledochal cyst of the lower end of the common bile duct. Pain, jaundice and tumour are the main symptoms.Until the advent of intravenous cholangiography, these lesions were seldom recognized preoperatively. Means of operative repair as well as complications and prognosis are reviewed.
机译:一名20岁妇女的胆总管近端有一个囊肿,左肝管有一个囊肿。这些病变在术前通过静脉胆道造影被诊断出并成功手术。在撰写本文时,她已被随访了一年。先天性胆道系统缺陷很少见,在文献回顾中,仅发现了两例与此相似的病例。人们普遍认为这些病变是先天性的,但确切的发病机理尚不清楚。Alonso-Lej,Rever和Pessagno 2 于1959年进行了文献综述,发现了403个真正的先天性肝管囊肿。最常见的先天性缺陷是胆总管下端的单个胆总管囊肿。疼痛,黄疸和肿瘤是主要症状。直到静脉胆管造影术问世之前,这些病变在术前很少被发现。回顾了手术修复的方法以及并发症和预后。

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