نتایج جستجو برای: tracheobronchopathia osteochondroplastica
تعداد نتایج: 139 فیلتر نتایج به سال:
1. Bioque JC, Feu N, Rubio JM, et al. Tracheobronchopathia osteochondroplastica – clinical study and follow-up in nine cases. Journal of Bronchology. 2001;8:78–83. 2. Pinto JA, Silva LC, Perfeito DJP, et al. Osteochondroplastic tracheobronchopathy: report on 02 cases and bibliographic review. Braz J Otorhinolaryngol. 2010;76:789–93. 3. Williams SM, Jones ET. General case of the day. Tracheobron...
Introduction: Tracheobronchopathia osteochondroplastica (TPO) is a rare benign disorder of the lower part of the trachea and the upper part of the main bronchi. Case Report: A case of tracheobronchopathia osteochondroplastica (TPO) diagnosed at the time of intubation in an intensive care unit due to difficulty when advancing the endotracheal tube beyond the vocal cords, is reported. A problem...
Tracheobronchopathia osteochondroplastica (TO) is considered an orphan disease with exceptional occurrence in children. We report a 5 year old female child who was referred to us with chronic cough and recurrent pneumonia. After several investigations, bronchoscopy showed multiple nodules in the tracheobronchial lumen, whose distribution was consistent with TO. The patient was followed for four...
Tracheobronchopathia osteochondroplastica (TO) is a rarely described disorder which historically has not been frequently recognized antemortem. Studies by computerized tomography (CT) and bronchoscopy now permit a definitive antemortem diagnosis and can obviate a more invasive diagnostic evaluation. We describe two cases of TO presenting as right middle lobe collapse, discuss the clinical and p...
Tracheobronchopathia osteochondroplastica (TBO) is a rare disease of unknown etiology characterised by a formation of multiple, cartilaginous and osteocartilaginous submucosal nodules in the trachea and major bronchi. The course of the disease is usually benign but the narrowing of the respiratory tract can lead to chronic non-specific clinical symptoms. We present a case of a 50-year old man w...
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