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先天性膈疝:相关畸形——囊性腺瘤样畸形、肺叶外隔离症和喉气管食管裂:两例报告

Congenital diaphragmatic hernia: associated malformations--cystic adenomatoid malformation, extralobular sequestration, and laryngotracheoesophageal cleft: two case reports.

作者信息

Ryan C A, Finer N N, Etches P C, Tierney A J, Peliowski A

机构信息

Department of Newborn Medicine, Royal Alexandra Hospital, Edmonton, Alberta, Canada.

出版信息

J Pediatr Surg. 1995 Jun;30(6):883-5. doi: 10.1016/0022-3468(95)90772-6.

Abstract

Two infants with unusual bronchopulmonary malformations associated with congenital diaphragmatic hernia (CDH) are presented. One infant had extralobular sequestration and cystic adenomatoid malformation of the lower lobe, in addition to a left-sided CDH. The second infant had a laryngotracheoesophageal cleft extending to the carina (type III) in addition to a left-sided CDH. These associated malformations can have major implications in terms of diagnosis, resuscitation, and surgical management of infants with CDH.

摘要

本文介绍了两名患有与先天性膈疝(CDH)相关的罕见支气管肺畸形的婴儿。一名婴儿除左侧CDH外,还患有肺叶外隔离症和下叶囊性腺瘤样畸形。第二名婴儿除左侧CDH外,还患有延伸至隆突的喉气管食管裂(III型)。这些相关畸形可能对CDH婴儿的诊断、复苏和手术管理产生重大影响。

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