Riva Giulio, Girolami Ilaria, Luchini Claudio, Villanova Manuela, Valotto Giovanni, Cima Luca, Carella Rodolfo, Riva Maurizio, Fraggetta Filippo, Novelli Luca, Eccher Albino
Pathology Unit, Department of Pathology and Diagnostics, University and Hospital Trust of Verona, Verona, Italy.
Department of Pathology, Central Hospital of Bolzano, Bolzano, Italy.
Am J Case Rep. 2019 Jan 18;20:74-77. doi: 10.12659/AJCR.911859.
BACKGROUND Tracheobronchopathia osteochondroplastica (TO) is a rare idiopathic disease with a stable course, which involves the lumen of the tracheobronchial tree. Clinical manifestations at time of presentation may differ, typically including hoarseness, persistent and/or productive cough, hemoptyses, and dyspnea. There are no well-established guidelines for diagnostic workup and treatment. Our aim here is to present a paradigmatic case of TO together with a concise survey of the most important clinical, radiological, and histological criteria. CASE REPORT We report a case of a 62-year-old non-smoker male with persisting cough and no prior history of respiratory disease. Chest radiography (RX) and computed tomography (CT) were unremarkable. Given the persistence of symptoms, the patient underwent bronchoscopic examination, which revealed protruding sessile nodules into the tracheal lumen, with cobblestone appearance. Histopathological examination of biopsies taken during bronchoscopy showed cartilaginous and osseous submucosal nodules consistent with the diagnosis of TO. CONCLUSIONS TO is not always an easily recognized disease, and a multidisciplinary team work is often required for diagnosis, with particular importance of endoscopic-pathological correlation.
背景 气管支气管骨软骨瘤病(TO)是一种病程稳定的罕见特发性疾病,累及气管支气管树管腔。发病时的临床表现可能各异,通常包括声音嘶哑、持续性和/或咳痰性咳嗽、咯血及呼吸困难。目前尚无完善的诊断检查和治疗指南。我们的目的是呈现一例TO的典型病例,并简要概述最重要的临床、放射学和组织学标准。病例报告 我们报告一例62岁不吸烟男性病例,该患者持续咳嗽,既往无呼吸系统疾病史。胸部X线(RX)和计算机断层扫描(CT)检查无异常。鉴于症状持续存在,患者接受了支气管镜检查,检查发现气管腔内有突出的无蒂结节,呈鹅卵石样外观。支气管镜检查时所取活检组织的组织病理学检查显示黏膜下软骨和骨结节,符合TO的诊断。结论 TO并非总是一种易于识别的疾病,诊断通常需要多学科团队协作,内镜-病理相关性尤为重要。