Agenesis of the Gallbladder: A Case Report

J. Ashindoitiang, C. Atimomo
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Abstract

Agenesis of gallbladder is rare. It may occur as isolated finding or in association with additional abnormalities. The overall incidence is between 0.01 and 0.04% but there is evidence of a much higher incidence in certain families suggesting a hereditary trait.(1,2) Encountering gallbladder agenesis during operation for gallbladder related pathology is a dilemma and a challenge to an astute surgeon to confirm the diagnosis by searching for it in ectopic sites and also to perform intra-operative cholangiography to locate it. Ectopic sites as listed by Sherson (3) include intrahepatic, left sided, between the leaves of lesser omentum, retroperitoneal and retrohepatic, within the falciform ligament, retroduodenal and retropancreatic. There are three groups of patients with agenesis of gallbladder, those with multiple anomalies, asymptomatic cases and symptomatic cases. Right upper quadrant pain occurs in 90% of the cases, nausea and vomiting in 60% and jaundice in 35%. (4) We treated a 30year old lady with agenesis of the gallbladder and obstructive jaundice.
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胆囊发育不全1例报告
胆囊发育不全是罕见的。它可能是孤立的发现,也可能与其他异常有关。胆囊发育不全的总发病率在0.01 - 0.04%之间,但有证据表明,在某些家族中发病率要高得多,这表明这是一种遗传特征。(1,2)在胆囊相关病理手术中遇到胆囊发育不全是一个难题,对一个精明的外科医生来说,通过在异位部位寻找胆囊发育不全并进行术中胆道造影定位胆囊发育不全是一个挑战。Sherson(3)列出的异位部位包括肝内、左侧、小网膜叶之间、腹膜后和肝后、镰状韧带内、十二指肠后和胰后。胆囊发育不全患者可分为多发异常患者、无症状患者和有症状患者。90%的病例出现右上腹部疼痛,60%的病例出现恶心和呕吐,35%的病例出现黄疸。我们治疗了一位胆囊发育不全并梗阻性黄疸的30岁妇女。
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