解剖异常导致气管受压1例:无名动脉综合征

Şule Gökçe, MD
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引用次数: 0

摘要

无名动脉压迫综合征是一种罕见的先天性异常。这种情况是鉴别诊断有嘈杂的呼吸,吠叫的咳嗽和呼气喘鸣的病人的重要考虑因素。在这里,我们报告一例无名动脉综合征,表现为持续和/或双相喘鸣在3个月大。本病例使我们强调明确识别血管异常的重要性,并再次强调详细病史和检查时观察/听呼吸的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Case Presented with Tracheal Compression Caused by An Anatomical Anomaly: The Innominate Artery Syndrome
Innominate artery compression syndrome is a rare congenital anomaly. The condition is an important consideration in the differential diagnosis of patients presenting with noisy breathing, a barky cough, and expiratory stridor. Here we report a case of Innominate Artery syndrome that presented with persistent and /or biphasic stridor in a 3-month-old. This case provides us to highlights the importance of unequivocally identifying the vascular anomalies and to emphasize once again the importance of detailed history and observing/hearing of the breathing during the examination.
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