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Tracheobronchopathia Osteochondroplastica: Two Cases Reports and Review of Literature

机译:气管支气管病Osteochondroplastica:两例报道并文献复习

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Tracheobronchopathia osteochondroplastica (TO) is a relatively rare and benign disease of unknown etiology that is characterized by the accumulation of diffuse cartilaginous and osseous nodules protruding into the anterolateral walls of the trachea and bronchus. However, TO is easy to ignore or misdiagnose due to its nonspecific clinical manifestation. A chest computed tomography (CT) scan with a fiber bronchoscope and pathological biopsy shows the clinical features supporting the ultimate diagnosis. Here, we report 2 misdiagnosed cases of TO and review the literature to further define the diagnosis for clinicians. The first case was a 34-year-old male admitted to the hospital because of recurrent cough and intermittent fever for 10 years. CT scans showed irregular stenosis of the main bronchus and bronchofibroscope showed multiple nodules producing into the lumen. He was initially misdiagnosed of bronchial tuberculosis and received antitubercular agents for nearly half year. Symptoms got no relief and another bronchofibroscope with biopsy tests in our hospital exactly diagnosed of TO. Symptoms were significantly relieved after receiving budesonide associated with antibiotics, etc. Another case was a 46-year-old woman presenting with a history of repeated hoarseness for 8 years and a 2-month exacerbation. She underwent an electronic laryngoscopy 3 times and was diagnosed of laryngitis. Symptoms got no relief after antiinflammatory. CT scan indicated variable degrees of stenosis and calcification of the distal trachea and main bronchi and bronchofibroscope showed dozens of white nodules extruding into the lumen. Histopathologic findings revealed the ultimate diagnosis of TO and antiinflammatories, spasm relievers, and inhaled corticosteroids, showed apparent effects. Poor specificity of TO is observed in clinical manifestation and laboratory inspection. However, a CT scan associated with a bronchoscopy and histopathologic examination greatly contributes to a definitive diagnosis. No specific treatments are recommended, except treatments to alleviate symptoms. Thus, it is of great importance to consider TO when facing unsolved respiratory or external respiratory symptoms to improve the quality of life.
机译:气管支气管病是一种病因不明的相对罕见和良性疾病,其特征是弥漫性的软骨和骨结节积聚,突出到气管和支气管的前外侧壁。但是,由于TO的非特异性临床表现,很容易忽略或误诊。使用纤维支气管镜进行的胸部计算机断层扫描(CT)扫描和病理活检显示支持最终诊断的临床特征。在这里,我们报告2例TO的误诊病例,并复习文献以进一步确定临床医生的诊断。第一例是一名因反复咳嗽和间歇性发烧10年而入院的34岁男性。 CT扫描显示主支气管不规则狭窄,支气管镜显示管腔内有多个结节。最初,他被误诊为支气管肺结核,并接受了近半年的抗结核药物治疗。症状没有缓解,我院另一支经活检的支气管镜准确诊断为TO。服用与抗生素等有关的布地奈德后,症状明显缓解。另一例是一名46岁的妇女,有反复嘶哑的病史,有8年的病史,且病情加重了2个月。她接受了电子喉镜检查3次,并被诊断出喉炎。抗炎后症状没有缓解。 CT扫描显示远端气管和主支气管的钙化程度不同,支气管镜显示数十个白色结节伸入管腔。组织病理学发现揭示了TO和消炎,痉挛缓解剂和吸入皮质类固醇的最终诊断,显示出明显的效果。在临床表现和实验室检查中观察到TO的特异性差。但是,与支气管镜检查和组织病理学检查相关的CT扫描极大地有助于明确诊断。除缓解症状的治疗外,不建议使用其他任何治疗方法。因此,在面对未解决的呼吸道症状或外部呼吸道症状时考虑使用TO至关重要,以改善生活质量。

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