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新生儿乙状结肠穿孔:低位肛门直肠畸形中的罕见病例及文献综述

Neonatal Sigmoid Colon Perforation: A Rare Occurrence in Low Anorectal Malformation and Review of the Literature.

作者信息

Parelkar Sandesh V, Kapadnis Satish P, Sanghvi Beejal V, Joshi Prashant B, Mundada Dinesh D, Oak Sanjay N

机构信息

Department of Pediatric Surgery, King Edward Memorial Hospital, Parel, Mumbai, India.

Department of Pediatric Surgery, King Edward Memorial Hospital, Parel, Mumbai, India.

出版信息

Pediatr Neonatol. 2016 Jun;57(3):232-5. doi: 10.1016/j.pedneo.2013.07.011. Epub 2013 Nov 11.

Abstract

Gastrointestinal perforation in neonates with anorectal malformation (ARM) is extremely uncommon. Delayed patient presentation is an important causative factor. A 2.5-kg neonate presented 72 hours after birth with abdominal distention and absent anal opening with meconium pearls. An abdominal X-ray revealed the presence of free gas. After adequate resuscitation patient underwent surgery. Closure of the sigmoid colon perforation with a proximal diverting loop colostomy with anoplasty was done. The literature reveals only two cases of sigmoid colon perforation with low ARM. Ours is the third case, in whom repair of the perforation and correction of the ARM was managed successfully at the same time.

摘要

患有肛门直肠畸形(ARM)的新生儿出现胃肠道穿孔极为罕见。患者就诊延迟是一个重要的致病因素。一名体重2.5千克的新生儿在出生72小时后出现腹胀,肛门未开口且有胎粪颗粒。腹部X线检查显示有游离气体。经过充分复苏后,患者接受了手术。采用近端转流性袢式结肠造口术并进行肛门成形术,对乙状结肠穿孔进行了闭合。文献中仅报道了两例低位ARM合并乙状结肠穿孔的病例。我们的病例是第三例,在此病例中,穿孔修复和ARM矫正同时成功完成。

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