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腹腔镜下再次审视胆囊缺如。

Agenesis of the gallbladder revisited laparoscopically.

作者信息

Azmat N, Francis K R, Mandava N, Pizzi W F

机构信息

Department of Surgery, Catholic Medical Center, Brooklyn, New York.

出版信息

Am J Gastroenterol. 1993 Aug;88(8):1269-70.

PMID:8338097
Abstract

Gallbladder agenesis is an extremely rare disease. Necropsy incidence has been reported to be 0.016%. Failure to locate the gallbladder at the time of a planned cholecystectomy can be very challenging. We report such a case during a laparoscopic cholecystectomy. The indication for surgery in these patients are complaints of gallbladder symptoms along with a false-positive ultrasound study. During exploration, an abnormal location of the gallbladder has to be excluded. Ectopic gallbladder locations include intrahepatic, lesser omentum, retroperitoneal, retrohepatic, within the falciform ligament, retroduodenal, and retrohepatic areas. Thorough exploration and cholangiography are essential. Embryologically, the gallbladder and cystic duct arise from the caudal portion of the hepatic bud. All of the previously reported cases of gallbladder agenesis have shown an absence of both the gallbladder and cystic duct. We report an embryological oddity wherein a patent cystic duct was found along with an agenetic gallbladder. This is the first case report of this finding, along with this being the first absent gallbladder discovered laparoscopically.

摘要

胆囊缺如是一种极为罕见的疾病。据报道,尸检发病率为0.016%。在计划进行胆囊切除术时未能找到胆囊可能极具挑战性。我们报告了一例在腹腔镜胆囊切除术中出现的此类病例。这些患者的手术指征是有胆囊症状的主诉以及超声检查结果呈假阳性。在探查过程中,必须排除胆囊位置异常的情况。异位胆囊位置包括肝内、小网膜、腹膜后、肝后、镰状韧带内、十二指肠后以及肝后区域。全面探查和胆管造影至关重要。从胚胎学角度来看,胆囊和胆囊管起源于肝芽的尾部。此前所有报道的胆囊缺如病例均显示胆囊和胆囊管均缺失。我们报告了一种胚胎学上的奇特现象,即发现了一条通畅的胆囊管以及一个缺如的胆囊。这是该发现的首例病例报告,同时也是首例通过腹腔镜发现的无胆囊病例。

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