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十二指肠门前静脉、旋转不良和高位空肠闭锁:一例报告。

Preduodenal portal vein, malrotation, and high jejunal atresia: a case report.

机构信息

Department of Pediatric Surgery and Urology, Medical University, 50-357 Wroclaw, Poland.

出版信息

J Pediatr Surg. 2012 Jan;47(1):e27-30. doi: 10.1016/j.jpedsurg.2011.09.059.

Abstract

Preduodenal portal vein (PDPV) is a rare congenital anomaly. In most patients, it is associated with other congenital defects including situs inversus, malrotation, and biliary atresia or occurs as part of the heterotaxia syndrome or polysplenia syndrome. We describe a newborn affected by high jejunal atresia, malrotation, and a complex cardiac anomaly, in whom PDPV was diagnosed at early relaparotomy because of stenosis of the jejunal anastomosis. Occurrence of PDPV with intestinal atresia has not been previously reported in the literature.

摘要

十二指肠门前静脉(PDPV)是一种罕见的先天性异常。在大多数患者中,它与其他先天性缺陷相关,包括内脏反位、旋转不良和胆道闭锁,或作为异位综合征或多脾综合征的一部分发生。我们描述了一例患有高位空肠闭锁、旋转不良和复杂心脏畸形的新生儿,由于空肠吻合口狭窄,在早期再次剖腹手术中诊断出 PDPV。文献中以前没有报道过 PDPV 与肠闭锁同时发生的情况。

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