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一名早产新生儿合并十二指肠空肠闭锁、背侧肠系膜缺如、胆总管囊肿及旋转不良——病例报告

Duodenojejunal atresia with absent dorsal mesentery, choledochal cyst, and malrotation in a premature newborn--a case report.

作者信息

Arbell Dan, Orkin Boris, Naveh Yaron, Gur Ilan, Udassin Raphael

机构信息

Department of Pediatric Surgery, Hadassah University Hospital, Jerusalem 91120, Israel.

出版信息

J Pediatr Surg. 2006 Jun;41(6):e11-3. doi: 10.1016/j.jpedsurg.2006.02.032.

Abstract

We present the case of a premature baby who was born with the following conditions: an extensive atresia from the first part of the duodenum to the mid small bowel; malrotation of the distal part, in volvulus and in an "apple peel" configuration; no connection of the bile ducts to the bowel; and presence of a type II choledochal cyst. To our knowledge, this is the first case in which a combination of these anomalies is reported. A brief review of the relevant literature is also presented.

摘要

我们报告了一例早产婴儿的病例,该婴儿出生时存在以下情况:十二指肠第一部至小肠中部广泛闭锁;远端肠管旋转不良,呈肠扭转及“苹果皮”样畸形;胆管与肠道无连接;存在II型胆总管囊肿。据我们所知,这是首例报道的合并这些异常情况的病例。本文还对相关文献进行了简要综述。

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