胆囊发育不全

Hamed Kabiri MD, Orville H. Domingo MD, Chris D. Tzarnas MD
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引用次数: 17

摘要

胆囊发育不全(胆管正常)是一种罕见的先天性疾病,10万人口中约有13 - 65人发生,可能是由于胆囊芽在子宫内发育或空泡化失败所致。有家族性倾向的报告可能建议筛查无症状的家庭成员,并在症状出现时加快治疗,从而避免手术。胆管结石在胆囊发育不全患者中是罕见的,发现的结石通常很小,并且患者总是首先表现为黄疸。作者描述了一例23岁患者胆囊发育不全和大胆总管结石,没有黄疸的表现。本文对相关文献进行了综述。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Agenesis of the Gallbladder

Agenesis of the gallbladder, with normal bile ducts, is a rare congenital condition occurring in 13 to 65 people out of a population of 100,000 and probably results from a failure of the gallbladder bud to develop or vacuolize in utero. Reports of a familial tendency toward this condition may suggest screening of asymptomatic family members and speed treatment when symptoms manifest, thus avoiding surgery. Choledocholithiasis in patients with gallbladder agenesis is rare, the stones found are usually small, and patients had invariably first presented with jaundice. The authors describe a case of a 23-year-old patient with gallbladder agenesis and a large choledochal calculus and without jaundice at presentation. A review of the literature is presented.

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