tracheobronchopathia osteochondroplastica
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2021 ◽  
Vol 60 (21) ◽  
pp. 3463-3467
Author(s):  
Jung Won Heo ◽  
Eung gu Lee ◽  
Bomi Gil ◽  
Hye Seon Kang ◽  
Yong Hyun Kim

2021 ◽  
pp. 014556132110516
Author(s):  
He Jiang ◽  
Xiaoying Yang ◽  
Ying Guo

We report two subjects with tracheobronchopathia osteochondroplastica (TO), including the clinical manifestations, histological findings, and clinical treatments, which were analyzed retrospectively. One patient with TO was a 60-year-old woman, and the other was a 47-year-old man. The main clinical manifestations were cough, chest pain, and dyspnea. Computed tomography (CT) images showed that TO mainly occurred in the trachea and main bronchus. Histological analysis showed inflammatory exudation, squamous metaplasia, submucosal cartilaginous, and ossification. We present the two cases to increase physician and patient awareness of this benign disease and to improve their understanding of the disease manifestations and potential complications.


2021 ◽  
Vol 14 (7) ◽  
pp. e243538
Author(s):  
Simon Proctor ◽  
Helen Crocker ◽  
Virginia Au ◽  
Vinod Aiyappan

An 81-year-old man presented with chronic cough, which did not respond to the initiation of combined bronchodilator/inhaled corticosteroid therapy. CT of the chest revealed calcified nodules throughout the trachea sparing the posterior membrane, and tiny peripheral parenchymal nodules with basal interlobular septal thickening and calcification. Flexible bronchoscopy demonstrated endobronchial nodularity from the proximal trachea to the mid-sections of both main bronchi, sparing the posterior membrane. Histopathology revealed submucosal fibrous connective tissue and benign bone, confirming a diagnosis of tracheobronchopathia osteochondroplastica. CT was consistent with a concurrent diagnosis of dendriform pulmonary ossification. These two rare phenomena often present with non-specific symptoms, and the diagnosis can be made with imaging in both conditions. There is a role for bronchoscopy in the diagnosis of tracheobronchopathia osteochondropastica, and the endobronchial appearance could be diagnostic. The concurrence of both phenomena in our case might represent activity of a common cellular pathway of ossification in both sites.


2021 ◽  
Vol 9 (7) ◽  
Author(s):  
Suat Yee Lim ◽  
Mohd Faizul Abu Samah ◽  
Lalitha Pereirasamy ◽  
Bee See Chew ◽  
Irfhan Ali Hyder Ali

2021 ◽  
Vol 14 (4) ◽  
pp. e240125
Author(s):  
Talha Shahzad ◽  
Nadeem Rizvi ◽  
Sabeeh Siddiqui ◽  
Rashida Ahmed

Tracheobronchopathia osteochondroplastica (TPO) is a rare disorder of the tracheopulmonary tree characterised by osseous and cartilaginous submucosal nodules projecting into the tracheal lumen, sparing the posterior tracheal membranous wall. Symptoms are non-specific and may include dry cough, hoarseness, dyspnoea, recurrent pneumonia and occasionally haemoptysis. A fibreoptic bronchoscopy showing multiple tracheal nodules followed by pathological biopsy is required to reach the final diagnosis. Here, we report two cases of TPO, both with history of biomass fuel exposure and almost similar clinical presentions with chronic cough, shortness of breath and intermittent haemoptysis. They both underwent fibreoptic bronchoscopy showing multiple tracheal nodules whose histopathological analysis showed the diagnosis of TPO. Both patients were treated conservatively and remained in good health afterwards. Physicians should be aware about the need of advanced surgical procedures including endotracheal stent placement in more severe cases.


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