Tracheobronchial amiloidosis
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Case Report
P: 119-121
September 2015

Tracheobronchial amiloidosis

İstanbul Med J 2015;16(3):119-121
1. Necmettin Erbakan Üniversitesi Meram Tıp Fakültesi, Göğüs Hastalıkları Anabilim Dalı, Konya, Türkiye
2. Konya Eğitim ve Araştırma Hastanesi, İç Hastalıkları Kliniği, Konya, Türkiye
3. Okmeydanı Eğitim ve Araştırma Hastanesi, Tıbbi Onkoloji Kliniği, İstanbul, Türkiye
No information available.
No information available
Received Date: 22.02.2015
Accepted Date: 18.05.2015
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ABSTRACT

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.

Keywords: Amyloidosis, pulmonary, tracheobronchial

References

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