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电视腹腔镜治疗胆囊管巨大囊肿:一例报告

Video-laparoscopic treatment of a sizeable cyst of the cystic duct: a case report.

作者信息

Bresciani C, Gama-Rodrigues J, Santos V R

机构信息

Hospital Evaldo Foz, University of São Paulo Medical School, Brazil.

出版信息

Surg Laparosc Endosc. 1998 Oct;8(5):376-9.

PMID:9799149
Abstract

A case of cystic dilation isolated from the cystic duct is described. The patient showed symptoms of chronic calculous cholecystitis; the ultrasonographic examination confirmed the clinical hypothesis and showed a 1.3-cm calculus impacted in the infundibulum of the gallbladder. The hepatic and biliary functions were normal. During surgery, the routine cholangiographic study showed a sizable cyst in the cystic canal, as well as an anomalous duct uniting the cyst to the right hepatic duct. As for the rest of the extrahepatic biliary canal, as well as the intrahepatic canal, nothing abnormal was noticed. The videolaparoscopic treatment consisted of a ligature with a clip of the cystic duct and the anomalous duct plus en bloc resection of the cyst and the gallbladder. Histopathologic study showed it to be a benign cyst and chronic calculous cholecystitis. It is important to establish the site of the cyst precisely before surgery, as the procedure should include its resection, since it could be the source of infection or development of lithiasis and even malignant degeneration. There are two hypotheses for the appearance of cysts in the biliary tract: congenital, due to a flaw in the multiplication of the cells that will form the biliary tract during the fetal life, and by aggression by pancreatic juice flowing back to the main biliary canal. The congenital origin seems to be the hypothesis that better explains the appearance of the cyst in the case described here, considering that the backflow of the pancreatic juice could hardly have occurred because of the anatomy as observed: the nonexistence of the common biliary-pancreatic canal and the valvular mechanism, present in the cystic canal, between the cyst itself and the confluence of the cystic canal into the main biliary canal, in addition to the anomalous biliary canal communicating the cyst to the right intrahepatic canal.

摘要

本文描述了一例源于胆囊管的囊性扩张病例。患者表现出慢性结石性胆囊炎的症状;超声检查证实了临床推测,并显示一枚1.3厘米的结石嵌顿于胆囊漏斗部。肝脏和胆汁功能正常。手术过程中,常规胆管造影研究显示胆囊管内有一个较大的囊肿,以及一条将囊肿与右肝管相连的异常胆管。至于肝外胆管的其余部分以及肝内胆管,未发现任何异常。电视腹腔镜治疗包括用夹子结扎胆囊管和异常胆管,外加整块切除囊肿和胆囊。组织病理学研究显示其为良性囊肿和慢性结石性胆囊炎。术前精确确定囊肿的位置很重要,因为手术应包括切除囊肿,因为它可能是感染源、结石形成的原因,甚至是恶性变的源头。胆管囊肿出现有两种假说:先天性的,是由于胎儿期形成胆管的细胞增殖存在缺陷;以及胰液反流至主胆管所致。考虑到从观察到的解剖结构来看,胰液反流几乎不可能发生:不存在胆总管 - 胰管共同通道,且胆囊管内存在瓣膜机制,位于囊肿本身与胆囊管汇入主胆管的汇合处之间,此外还有一条将囊肿与右肝内胆管相连的异常胆管,先天性起源似乎是能更好解释此处所述病例中囊肿出现的假说。

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