| Literature DB >> 16615021 |
Ercüment Ege1, Esra Uzaslan, Ahmet Ursavaş, Metin Güçlü, Fahir Ozkalemkaş, Sahsine Tolunay.
Abstract
Amyloidosis is a syndrome characterized by the deposition of an insoluble proteinaceous material in the extracellular matrix of one or several organs. Respiratory tract involvement with amyloid is rare and deposition of lower respiratory tract has been recognized in a variety of situations with different presentations. Primary idiopathic amyloidosis may be a diagnostic problem because of its low incidence and its variable manifestations. We report herein a case with multiple myeloma presenting diffuse interstitial infiltration, in which pulmonary AL type amyloidosis was diagnosed through transbronchial lung biopsy.Entities:
Mesh:
Year: 2006 PMID: 16615021
Source DB: PubMed Journal: Tuberk Toraks ISSN: 0494-1373