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骨化性气管支气管病:罕见但不容忽视。

Tracheobronchopathia osteochondroplastica: rare but not to be forgotten.

作者信息

Gul Fahad, Peterson Eric, Dejoy Robert, Eiger Glenn, Mora Carpio Andres, Gupta Ena

机构信息

Department of Internal Medicine Einstein Medical Center Philadelphia PA USA.

Department of Pulmonary and Critical Care Einstein Medical Center Philadelphia PA USA.

出版信息

Respirol Case Rep. 2020 Jun 26;8(6):e00609. doi: 10.1002/rcr2.609. eCollection 2020 Aug.

Abstract

We report a case of a 59-year-old male with a one-month history of pleuritic chest pain who was diagnosed with tracheobronchopathia osteochondroplastica (TO). TO is a rare benign condition characterized by protruding submucosal nodules into the tracheobronchial lumen. The disease is generally asymptomatic, with rare cases of progressive nodularity, cough, dyspnoea, and haemoptysis. Diagnosis can be made via bronchoscopic visualization of bony and cartilaginous nodules on tracheal walls. Although generally benign, the rarity of this condition makes diagnosis difficult even for trained pulmonologists and frequently predisposes patients to unnecessary invasive diagnostic testing and improper management of symptoms and contributing co-morbid conditions. We present this case to increase physician and patient awareness about this disease to help improve diagnostic strategy and knowledge of disease manifestations and potential complications.

摘要

我们报告一例59岁男性,有1个月的胸膜炎性胸痛病史,被诊断为骨软骨瘤性气管支气管病(TO)。TO是一种罕见的良性疾病,其特征是黏膜下结节突入气管支气管腔内。该病通常无症状,仅有罕见的进行性结节形成、咳嗽、呼吸困难和咯血病例。可通过支气管镜观察气管壁上的骨和软骨结节来进行诊断。尽管该病通常为良性,但因其罕见,即使对于训练有素的肺科医生来说诊断也很困难,且常常使患者接受不必要的侵入性诊断检查以及对症状和相关合并症的不当处理。我们展示此病例以提高医生和患者对该疾病的认识,有助于改进诊断策略以及对疾病表现和潜在并发症的了解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09d5/7317299/1b06b11186f2/RCR2-8-e00609-g001.jpg

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