İstanbul Medical Journal (Sep 2015)

Tracheobronchial amiloidosis

  • Soner Demirbaş,
  • Orkide Kutlu,
  • Abdullah Sakin

DOI
https://doi.org/10.5152/imj.2015.76588
Journal volume & issue
Vol. 16, no. 3
pp. 119 – 121

Abstract

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Localized pulmonary amyloidosis without systemic involvement differentiates as nodular parenchymal opacities, diffuse parenchymal opacities, or tracheobronchial amyloidosis (TBA). TBA is a condition mostly seen in males aged up to 50–60 years, accounting for approximately 1% of benign lesions in the tracheobronchial tree. TBA is characterized by the accumulation of the amyloid material comprising immunoglobulin light chain (AL), which are observed as submucosal plaques and/or polypoid tumors; progressive form of tracheobronchial amyloidosis can lead to airway obstruction. Repeated excisional treatments, mainly laser treatment is preferable to open surgery. Here, we have presented the case of a patient diagnosed with the rarely occurring localized TBA.

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