先天性空肠和回肠缺失：一例病例报告及文献综述

Congenital absence of jejunum and ileum: A case report and literature review.

作者信息

Tripathy Prasanta Kumar, Ray Banoj Kumar, Mohanty Hiranya Kishore

机构信息

Department of Pediatric Surgery, SVP Postgraduate Institute of Pediatrics, Cuttack, Odisha, India.

出版信息

Afr J Paediatr Surg. 2017 Jul-Sep;14(3):53-55. doi: 10.4103/ajps.AJPS_63_16.

DOI:10.4103/ajps.AJPS_63_16

PMID:29557352

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5881287/

Abstract

We report an extremely rare finding 'congenital absence of jejunum and ileum' during explorative laparotomy of a 16-day-old female neonate. The dilated duodenum was terminating blindly, and the next segment of intestine was a peanut-sized cecum followed by microcolon. On an extensive survey of literature this type of intestinal atresia is not reported in living babies.

摘要

我们报告了一例极为罕见的病例，在对一名16天大的女新生儿进行剖腹探查术时发现“空肠和回肠先天性缺失”。扩张的十二指肠呈盲端终止，下一段肠道是花生大小的盲肠，其后是小结肠。在广泛查阅文献后发现，尚无活产婴儿出现这种类型肠闭锁的报道。