Tracheobronchopathia osteochondroplastica
Updates to Article Attributes
Tracheobronchopathia osteochondroplastica (TO) is a very rare idiopathic non neoplastic tracheo-bronchial abnormality.
Epidemiology
The estimated prevalence on routine bronchoscopy can be upto 0.7% . It typically affects those in the 5th to 6th decades and there may be a male predilection 4.
Clinical presentation
Most patients are asymptomatic. Those who have symptoms may present with cough, shortness of breath on exertion, wheezing or recurrent respiratory infection. Haemoptysis can occasionally result from an ulceration of a nodule or an acute infection.
Pathology
There is development of osseous or cartilaginous 1-8mm 2-3 nodules or both in the submucosa of the trachea and bronchial walls. They may be either focal or diffuse. There is characterisitic sparing the posterior membranous portions of the trachea 6.
There are two possible theories of pathogenesis:
- ecchondrosis and exostosis from cartilage rings
- cartilaginous and osseous metaplasia of the elastic tissue in the internal elastic fibrous membrane.
Location
- classically affects the lower 2/3rds of the trachea and proximal portions of the bronchi 4.
- only affects the anterior and lateral walls.
Radiographic features
Chest radiograph
May show irregularity and narrowing of the typically affected segments of the trachea and bronchi.
CT
May additionally show thickened tracheal cartilages with sparing of posterior membranous portions. There are small (typically ~3-8 mm) calcific nodules along its inner tracheal aspect, protruding into the tracheal lumen. The appearance is much more irregular than that seen with normal cartilage calcification.
History and etymology
Initially described in 1857 by SSamuel Wilks in 1857(1824-1911), as ossific"ossific deposits in the larynx, trachea and bronchi" in a 38-year-old-male who died of pulmonary tuberculosis 5. The condition was later termed "tracheopathia osteochondroplastica" in 1910 by German pathologist Karl Ludwig Aschoff (1866-1942) 5.
Treatment and prognosis
It is a benign condition and often no interventional in required in asymptomatic cases. Successful recovery with NSAIDS and Dapsonedapsone have been reported in symptomatic cases. Overall prognosis is generally good and is dependent upon airway stenosis caused by nodules.
Differential diagnosis
Imaging differential considerations include:
- tracheobronchial amyloidosis: involves the posterior membranous portion of the trachea
- relapsing polychondritis: spares the posterior membranous portion of the trachea
-</ul><h4>Radiographic features</h4><h5>Chest radiograph</h5><p>May show irregularity and narrowing of the typically affected segments of the trachea and bronchi.</p><h5>CT</h5><p>May additionally show thickened tracheal cartilages with sparing of posterior membranous portions. There are small (typically ~3-8 mm) calcific nodules along its inner tracheal aspect, protruding into the tracheal lumen. The appearance is much more irregular than that seen with normal cartilage calcification.</p><h4>History and etymology</h4><p>Initially described by <strong>S Wilks</strong> in 1857 as ossific deposits <sup>5</sup>.</p><h4>Treatment and prognosis</h4><p>It is a benign condition and often no interventional in required in asymptomatic cases. Successful recovery with NSAIDS and Dapsone have been reported in symptomatic cases. Overall prognosis is generally good and is dependent upon airway stenosis caused by nodules. </p><h4>Differential diagnosis</h4><p>Imaging differential considerations include:</p><ul>- +</ul><h4>Radiographic features</h4><h5>Chest radiograph</h5><p>May show irregularity and narrowing of the typically affected segments of the trachea and bronchi.</p><h5>CT</h5><p>May additionally show thickened tracheal cartilages with sparing of posterior membranous portions. There are small (typically ~3-8 mm) calcific nodules along its inner tracheal aspect, protruding into the tracheal lumen. The appearance is much more irregular than that seen with normal cartilage calcification.</p><h4>History and etymology</h4><p>Initially described in 1857 by <strong>Samuel Wilks</strong> (1824-1911), as "ossific deposits in the larynx, trachea and bronchi" in a 38-year-old-male who died of pulmonary tuberculosis <sup>5</sup>. The condition was later termed "tracheopathia osteochondroplastica" in 1910 by German pathologist <strong>Karl Ludwig Aschoff</strong> (1866-1942) 5.</p><h4>Treatment and prognosis</h4><p>It is a benign condition and often no interventional in required in asymptomatic cases. Successful recovery with NSAIDS and dapsone have been reported in symptomatic cases. Overall prognosis is generally good and is dependent upon airway stenosis caused by nodules. </p><h4>Differential diagnosis</h4><p>Imaging differential considerations include:</p><ul>
References changed:
- 5. Sakula A. Tracheobronchopathia Osteoplastica: Its Relationship to Primary Tracheobronchial Amyloidosis. Thorax. 1968;23(1):105-10. <a href="https://doi.org/10.1136/thx.23.1.105">doi:10.1136/thx.23.1.105</a> - <a href="https://www.ncbi.nlm.nih.gov/pubmed/4966103">Pubmed</a>
- 5. Wilks S. Ossific deposits on the larynx, trachea and bronchi. Trans Pathol Soc Lond 1857; 8:88.