喉闭锁、气管发育不全、气管-食管瘘、右心室双出口及持续性左上腔静脉1例

Journal of neonatal biology Pub Date : 2015-08-10 DOI:10.4172/2167-0897.1000186

Hesham Al-Saloos

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引用次数: 1

摘要

先天性高气道阻塞综合征(CHAOS)包括喉闭锁和气管发育不全，这是一种罕见且可能致命的疾病。我们描述了一个新生儿足月婴儿喉闭锁和气管发育不全远端气管食管瘘(TEF)。他还有双出口右心室(DORV)和持续性左上腔静脉(LSVC)。据我们所知，这是该协会的第一份报告。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

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Case of Laryngeal Atresia, Tracheal Agenesis, Tracheo-Esophageal Fistula, Double Outlet Right Ventricle and Persistent Left Superior Vena Cava

Congenital high airway obstruction syndrome (CHAOS) includes laryngeal atresia and tracheal agenesis which are rare and potentially lethal conditions. We describe a newborn term infant with laryngeal atresia and tracheal agenesis with a distal tracheo-esophageal fistula (TEF). He also had a double outlet right ventricle (DORV) and a persistent left superior vena cava (LSVC). To our knowledge this is the first report of this association.

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Journal of neonatal biology

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