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小肠先天性异常:综述与更新

Small Bowel Congenital Anomalies: a Review and Update.

作者信息

Morris Grant, Kennedy Alfred, Cochran William

机构信息

Department of Pediatrics, Geisinger Clinic, 100 N. Academy Avenue, Danville, PA, 17822, USA.

Department of Pediatric Surgery, Geisinger Clinic, 100 N. Academy Avenue, Danville, PA, 17822, USA.

出版信息

Curr Gastroenterol Rep. 2016 Apr;18(4):16. doi: 10.1007/s11894-016-0490-4.

Abstract

The small intestine is a complex organ system that is vital to the life of the individual. There are a number of congenital anomalies that occur and present most commonly in infancy; however, some may not present until adulthood. Most congenital anomalies of the small intestine will present with obstructive symptoms while some may present with vomiting, abdominal pain, and/or gastrointestinal bleeding. Various radiologic procedures can aid in the diagnosis of these lesions that vary depending on the particular anomaly. Definitive therapy for these congenial anomalies is surgical, and in some cases, surgery needs to be performed urgently. The overall prognosis of congenital anomalies of the small intestine is very good and has improved with improved medical management and the advent of newer surgical modalities. The congenital anomalies of the small intestine reviewed in this article include malrotation, Meckel's diverticulum, duodenal web, duodenal atresia, jejunoileal atresia, and duplications.

摘要

小肠是一个对个体生命至关重要的复杂器官系统。有多种先天性异常情况,最常见于婴儿期出现;然而,有些可能直到成年才会表现出来。大多数小肠先天性异常会表现出梗阻症状,而有些可能表现为呕吐、腹痛和/或胃肠道出血。各种放射学检查方法有助于诊断这些因特定异常而各异的病变。这些先天性异常的确定性治疗方法是手术,在某些情况下,需要紧急进行手术。小肠先天性异常的总体预后非常好,随着医疗管理的改善和更新的手术方式的出现,预后有所改善。本文所综述的小肠先天性异常包括肠旋转不良、梅克尔憩室、十二指肠蹼、十二指肠闭锁、空肠回肠闭锁和重复畸形。

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