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与肛门直肠畸形相关的消化道闭锁:十年经验

Alimentary Tract Atresias associated with Anorectal Malformations: 10 Years' Experience.

作者信息

Saha Manoj

机构信息

Department of Pediatric Surgery, Gauhati Medical College, GUWAHATI, ASSAM, INDIA.

出版信息

J Neonatal Surg. 2016 Oct 10;5(4):43. doi: 10.21699/jns.v5i4.449. eCollection 2016 Oct-Dec.

Abstract

Anorectal malformation (ARM) is one of the most common congenital anomaly that requires emergency surgery in the neonatal period. ARMs are frequently associated with other life threatening congenital anomalies. Commonly associated anomalies are genito-urinary, cardiovascular, gastro-intestinal, skeletal and spinal. Alimentary tract anomalies are frequently masked by the intestinal obstruction produced by the anorectal atresia. This retrospective study was carried out to find out the incidence of associated alimentary tract atresias with ARM. In our series, out of 785 cases of high ARM, 14 cases had associated esophageal atresia (1.8%), followed by 7 cases of duodenal atresia (0.89%), and followed by pyloric atresia, jejuno-ileal atresia and colonic atresia.

摘要

肛门直肠畸形(ARM)是最常见的先天性异常之一,需要在新生儿期进行急诊手术。ARM常与其他危及生命的先天性异常相关。常见的相关异常包括泌尿生殖系统、心血管系统、胃肠道、骨骼和脊柱方面的异常。消化道异常常被肛门直肠闭锁引起的肠梗阻所掩盖。本回顾性研究旨在找出ARM合并消化道闭锁的发生率。在我们的系列研究中,785例高位ARM病例中,14例合并食管闭锁(1.8%),其次是7例十二指肠闭锁(0.89%),然后是幽门闭锁、空肠回肠闭锁和结肠闭锁。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eceb/5117266/4ba5ed36b1e4/jns-5-43.f1.jpg

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