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[先天性胆囊重复畸形。一例罕见的小梁状胆囊病例]

[Congenital duplication of the gallbladder. A rare case of a trabecular gallbladder].

作者信息

Lugaresi M L, Principe A, Mazziotti A, Ruberto F

机构信息

Istituto di Clinica Chirurgica II, Università degli Studi di Bologna.

出版信息

Minerva Chir. 1994 May;49(5):475-9.

PMID:7970048
Abstract

Duplication of the gallbladder is a congenital anomaly of rare preoperative diagnostic finding, which could be present in an asymptomatic or symptomatic form. The authors report a case of double gallbladder, which becomes clinically manifest through repeated biliary colics. The preoperative diagnostic procedures did not reveal the malformation, but only the presence of lithiasis in one of the gallbladders, in the common bile duct and, for an anomalous insertion of the cystic duct, a suspect cancer of the distal choledochus.

摘要

胆囊重复是一种先天性异常,术前诊断发现罕见,可表现为无症状或有症状形式。作者报告一例双胆囊病例,其通过反复胆绞痛临床表现出来。术前诊断程序未发现畸形,仅发现其中一个胆囊、胆总管有结石,且由于胆囊管异常插入,怀疑胆总管远端有癌症。

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