Unique Approach to Diagnosing and Treating Congenital Bronchial Atresia (CBA): A Case Series

A. Mahajan, Rod A Rahimi, Paul, erlaan, Erik Folch, S. Gangadharan, A. Majid
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引用次数: 2

Abstract

Congenital bronchial atresia (CBA) is a rare airway anomaly resulting in termination of a bronchus into a blind pouch with associated mucoid impaction and segmental hyperinflation. The etiology of CBA is related to vascular insufficiency to the bronchial bud during embryologic development. Controversy exists regarding the best approach to treatment for CBA and relating symptoms to the presence of these anomalies can be challenging. This case series describes three patients with varying approaches to diagnosis and treatment of CBA.
诊断和治疗先天性支气管闭锁(CBA)的独特方法:一个病例系列
先天性支气管闭锁(CBA)是一种罕见的气道异常,导致支气管终止进入盲袋,并伴有黏液嵌塞和节段性过度膨胀。CBA的病因与胚胎发育过程中支气管芽血管功能不全有关。关于CBA的最佳治疗方法存在争议,并且将症状与这些异常的存在联系起来可能具有挑战性。本病例系列描述了三个不同的CBA诊断和治疗方法的患者。
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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