Tracheobronchopathia osteochondroplastica: Case report of a rare cause for a common symptom

Supriya Adiody, Krishnanand Krishnakumar, Sruthi Raghunath, Aravind Thayyil Raman
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引用次数: 0

Abstract

Tracheobronchopathia osteochondroplastica is a rare disease which is characterised by the presence of osseous and/or cartilaginous submucosal nodules projecting into the anterior and lateral walls of the airways. We present the case of a 56-year-old male presenting with chronic cough, dyspnoea and haemoptysis. An initial diagnosis of tuberculosis was kept in mind considering the endemicity of the disease. A fibre optic bronchoscopy, however helped in clinching the diagnosis. As there are no guidelines for the treatment, conservative treatment with inhaled steroids,bronchodilators, antibiotics, and avoidance of the airwayirritants, is sufficient for the patient. On follow up after 2 months patient is doing fine with symptomatic improvement.
气管支气管软骨发育不良:常见症状的罕见病因病例报告
气管软骨发育不全是一种罕见疾病,其特征是气管前壁和侧壁出现骨质和/或软骨质粘膜下结节。本病例是一名 56 岁的男性,表现为慢性咳嗽、呼吸困难和咯血。考虑到肺结核的流行性,初步诊断为肺结核。然而,纤维支气管镜检查有助于确诊。由于没有治疗指南,患者只需接受吸入类固醇、支气管扩张剂和抗生素的保守治疗,并避免使用气道刺激物。2 个月后的随访显示,患者症状有所改善,情况良好。
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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