Tracheobronchial Amiloidosis

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dc.contributor.authorDemirbas, Soner
dc.contributor.authorKutlu, Orkide
dc.contributor.authorSakin, Abdullah
dc.date.accessioned2024-02-23T14:41:07Z
dc.date.available2024-02-23T14:41:07Z
dc.date.issued2015
dc.departmentNEÜen_US
dc.description.abstractLocalized 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.en_US
dc.identifier.doi10.5152/imj.2015.76588
dc.identifier.endpage121en_US
dc.identifier.issn1304-8503
dc.identifier.issn2148-094X
dc.identifier.issue3en_US
dc.identifier.startpage119en_US
dc.identifier.urihttps://doi.org/10.5152/imj.2015.76588
dc.identifier.urihttps://hdl.handle.net/20.500.12452/16723
dc.identifier.volume16en_US
dc.identifier.wosWOS:000421133400008en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.language.isoenen_US
dc.publisherAvesen_US
dc.relation.ispartofIstanbul Medical Journalen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectAmyloidosisen_US
dc.subjectPulmonaryen_US
dc.subjectTracheobronchialen_US
dc.titleTracheobronchial Amiloidosisen_US
dc.typeArticleen_US

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