Suppr超能文献

先天性短肠综合征:新生儿肠梗阻的罕见病因。

Congenital short bowel syndrome: a rare cause of neonatal intestinal obstruction.

机构信息

Pediatric Surgery, Alexandria Faculty of Medicine, Alexandria, Egypt.

出版信息

J Int Med Res. 2020 Sep;48(9):300060520954726. doi: 10.1177/0300060520954726.

Abstract

Congenital short bowel syndrome (CSBS) is an uncommon gastrointestinal disorder in which an unclear aetiology causes considerable intrauterine reduction in small bowel length. As a result of reduced absorptive intestinal length, chronic diarrhoea, vomiting, and consequently, failure to thrive are likely. We report a case of CSBS in a 26-day-old girl who had malrotation and a short bowel with a length of bowel from the pylorus to the ileocecal junction of approximately 40 cm. The patient underwent Ladd's procedure, but she is still dependent on parenteral nutrition.

摘要

先天性短肠综合征(CSBS)是一种罕见的胃肠道疾病,其病因不明,导致胎儿期小肠长度明显缩短。由于吸收肠段缩短,患儿可能出现慢性腹泻、呕吐,继而导致生长不良。我们报告了一例 26 天大的女婴 CSBS 病例,该患儿存在肠旋转不良和短肠,从幽门至回盲部的肠管长度约为 40cm。患儿接受了 Ladd 手术,但仍依赖于肠外营养。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac4f/7509730/dca87cfbb092/10.1177_0300060520954726-fig1.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验