Tracheobronchomegaly (Mounier-Kuhn Syndrome) in Old Age - A Case Report

Khawaja Bilal Waheed, Jawad Nasser, Raghad Hamdi Alsaidalani, Zubair Ahmed
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Abstract

Tracheobronchomegaly or Mounier-Kuhn syndrome is a rare condition affecting the airways and is characterized by dilatation of the trachea and major bronchi secondary to atrophic or absent elastic fibres of the cartilage and thinning of the muscles.[1] The abnormally enlarged flaccid portions of the bronchial tree collapse and fail to maintain patency during expiration and coughing, predisposing the patient to stagnation of contents and recurrent lower respiratory tract infections, emphysema, bronchiectasis and chronic pulmonary suppuration.[2] The diagnosis is usually made on basis of specific radiographic features,[3] particularly on computed tomography (CT) scan. We report a case of a 69-year-old man who presented with recurrent lower respiratory tract infections and was found to have tracheobronchomegaly as an underlying primary airway abnormality on imaging and bronchoscopy that was initially undiagnosed.
老年气管支气管扩张症(Mounier-Kuhn综合征)一例报告
气管支气管肥大或Mounier-Kuhn综合征是一种影响气道的罕见疾病,其特征是继发于软骨弹性纤维萎缩或缺失和肌肉变薄的气管和主支气管扩张。[1] 支气管树异常增大的松弛部分在呼气和咳嗽时塌陷,无法保持通畅,使患者容易出现内容物停滞和反复出现下呼吸道感染、肺气肿、支气管扩张和慢性肺部化脓。[2] 诊断通常基于特定的放射学特征,[3]特别是计算机断层扫描(CT)。我们报告了一例69岁的男性患者,他出现反复的下呼吸道感染,并在成像和支气管镜检查中发现气管支气管扩张是一种潜在的原发性气道异常,最初未被诊断。
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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