Hantous-Zannad S, Sebaï L, Zidi A, Ben Khelil J, Mestiri I, Besbes M, Hamzaoui A, Ben Miled-M'rad K
Department of Radiology, Abderrahmane Mami Hospital, Ariana 2080, Tunisia.
Eur J Radiol. 2003 Feb;45(2):113-6. doi: 10.1016/s0720-048x(02)00028-1.
Tracheobronchopathia osteochondroplastica (TO) is a rare benign disorder affecting the trachea and occasionally the bronchi. We report a case of TO presenting as a respiratory insufficiency. Chest radiograph revealed an irregular narrowing of the intra thoracic trachea and a parenchymal consolidation of the left lower lobe. Magnetic resonance examination of the chest showed a diffuse irregular thickening of the trachea and central bronchi, which had an intermediate signal intensity with punctiform low signal intensity suggesting calcifications and no contrast enhancement. The diagnosis was confirmed by bronchoscopy and biopsies.
骨化性气管支气管病(TO)是一种罕见的良性疾病,累及气管,偶尔也会累及支气管。我们报告一例以呼吸功能不全为表现的TO病例。胸部X线片显示胸段气管不规则狭窄及左肺下叶实质实变。胸部磁共振检查显示气管和中央支气管弥漫性不规则增厚,信号强度中等,伴有点状低信号,提示钙化,无强化。支气管镜检查和活检确诊了该诊断。