先天性幽门闭锁。三例病例报告[作者简介]。

H Dodat, J M Pouillaude, H Renaud, J P Chappuis, M Daudet
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引用次数: 0

摘要

先天性幽门闭锁是一种相对少见的疾病。作者从三个病例中指出了诊断依据。主要临床表现为羊水、早期非胆汁性呕吐及腹胀。诊断基于腹部平片。他们显示胃膨胀,幽门末端没有空气。当胶片可以在直立位置拍摄时,它们显示一个单一的胃内空气-流体水平。放射学的发现是必要的,因为手术检查不能单独证明膜性闭锁和冠状闭锁比全闭锁更常见。在前两种情况下,放射学表现引导外科医生通过幽门近腔切开引入导管寻找梗阻。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Congenital pyloric atresia. Report of three cases (author's transl)].

Congenital pyloric atresia is a relatively unusual condition. From three cases the authors point out the diagnosis basis. The main clinical findings are hydramnios, early non bilious vomiting and epigastric distension. Diagnosis is based upon abdominal plain films. They demonstrate an air dilated stomach, and no air distal to the pylorus. When films can be taken in the upright position, they demonstrate a single intragastric air-fluid level. Radiologic findings are essential, because surgical inspection alone fails to demonstrate membranous atresia and cordonal atresia which are more frequent than total atresia. In the two former conditions, radiologic findings lead the surgeon to look for the obstruction by the mean of a catheter introduced by a juxta-pyloric antrotomy.

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