先天性胃畸形

T. Yandza (Praticien hospitalier) , J. Valayer (Professeur honoraire des Universités)
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引用次数: 4

摘要

胃的先天性异常同样多样且罕见。它们可以通过产前超声检查发现,也可以在成年后期发现中度或非阻塞性,没有炎症累及。胃重复是消化道所有重复中最不常见的;幽门闭锁及其变种通常在出生后一开始喂养就有症状。无症状的异常胰岛在剖腹手术时很常见,但当靠近幽门时,它们可能引起阻塞性症状。至于胃憩室,有些不应认为是在病理范围内;无论如何,它们在成年人中更常见。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Malformations congénitales de l'estomac

Congenital anomalies of the stomach are equally varied and infrequent. They may be discovered either by prenatal ultrasound investigations, or later during adulthood for those moderately or not obstructive, and without inflammatory involvement. Gastric duplications are the least frequent of all duplications of the alimentary tract; pyloric atresia and its variants are usually symptomatic at birth as soon as feeding is initiated. Asymptomatic aberrant pancreatic islets are quite commonly found at laparotomy, but when next to the pylorus, they may cause obstructive symptoms. As for gastric diverticulae, some should not be considered as within limits of a pathological condition; they are anyway more frequently encountered in adults.

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