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先天性胆囊缺如:避免剖腹手术的方法

Congenital absence of the gallbladder: ways of avoiding laparotomy.

作者信息

Akoh J A, George M M, Auld C D, Walls A D

机构信息

Dumfries and Galloway Royal Infirmary.

出版信息

Br J Clin Pract. 1994 Mar-Apr;48(2):77-8.

PMID:8024996
Abstract

Two cases of congenital absence (agenesis) of the gallbladder seen at one hospital over a 5-year period are presented. One patient presented with ascending cholangitis due to choledocholithiasis, while the other presented with right upper quadrant abdominal pain and equivocal findings on ultrasound and oral cholecystography. Although diagnosis was made at laparotomy in both cases, it is likely that the arrival of laparoscopic cholecystectomy will avoid laparotomy in the future. The place of laparoscopy in establishing the presence of this anomaly is discussed.

摘要

本文介绍了一家医院在5年时间内收治的2例先天性胆囊缺如(发育不全)病例。1例患者因胆总管结石出现化脓性胆管炎,另1例患者表现为右上腹疼痛,超声和口服胆囊造影检查结果不明确。尽管两例均在剖腹手术时确诊,但随着腹腔镜胆囊切除术的出现,未来很可能避免进行剖腹手术。文中还讨论了腹腔镜检查在诊断这种异常情况中的作用。

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