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婴儿胆结石:一例报告。

Infant cholelithiasis: report of a case.

作者信息

Asabe K, Handa N

机构信息

Department of Pediatric Surgery, Oita Prefectural Hospital, Japan.

出版信息

Surg Today. 1997;27(1):71-5. doi: 10.1007/BF01366944.

Abstract

Cholelithiasis is an extremely unusual finding in infancy. The following article describes the case of a 2-month-old male with a VACTER association who presented with persistent and progressive obstructive jaundice and acholic stool due to cholelithiasis. Thirty cases under the age of 1, including our case, have previously been reported in the Japanese literature. Twenty-eight cases had predisposing factors. The calculi were present only in the gallbladder in 18 cases, in the common bile duct or cystic duct or both in 7 cases, and in the gallbladder and common bile duct in 3 cases. Ten cases of stones were radiopaque, which thus made the plain abdominal roentgenogram findings very valuable. Nine cases underwent operation including cholecystectomy in 3 cases, choledocholithotomy in 3 cases, and cholecystolithotomy in 1 case, while the procedure was unknown in 2 cases. Recently, the number of reported cases of cholelithiasis in infants has gradually increased and today these cases are most often diagnosed by ultrasonography, because the examination is easy to perform and not invasive.

摘要

胆结石在婴儿期是一种极其罕见的病症。以下文章描述了一名患有VACTER综合征的2个月大男性病例,该患儿因胆结石出现持续性进行性梗阻性黄疸和无胆汁粪便。此前日本文献报道过包括我们这个病例在内的1岁以下的30个病例。28个病例有诱发因素。结石仅存在于胆囊的有18例,存在于胆总管或胆囊管或两者皆有的有7例,存在于胆囊和胆总管的有3例。10例结石是不透X线的,因此腹部平片的检查结果非常有价值。9例接受了手术,其中3例行胆囊切除术,3例行胆总管切开取石术,1例行胆囊切开取石术,2例手术方式不明。最近,婴儿胆结石的报告病例数逐渐增加,如今这些病例大多通过超声检查诊断,因为该检查操作简便且无创。

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