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[先天性幽门闭锁。三例报告(作者译)]

[Congenital pyloric atresia. Report of three cases (author's transl)].

作者信息

Dodat H, Pouillaude J M, Renaud H, Chappuis J P, Daudet M

出版信息

J Radiol Electrol Med Nucl. 1978 Oct;59(10):567-70.

PMID:745172
Abstract

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.

摘要

先天性幽门闭锁是一种相对罕见的病症。作者通过三例病例指出了诊断依据。主要临床症状为羊水过多、早期非胆汁性呕吐和上腹部膨隆。诊断基于腹部平片。平片显示胃扩张且幽门远端无气体。当能拍摄立位片时,可见胃内单一气液平面。放射学检查结果至关重要,因为仅通过手术探查无法发现比完全闭锁更常见的膜性闭锁和条索状闭锁。在前两种情况下,放射学检查结果引导外科医生通过经幽门旁胃窦切开术插入导管来寻找梗阻部位。

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