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Localized nasopharyngeal amyloidosis: A case report

Amyloidosis is a rare condition on its own but finding localized amyloidosis of a site such as the nasopharynx is an extremely rare condition with very few cases described in the literature. The condition occurs due to the accumulation of misfolded proteins in the extracellular space disrupting the...

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Detalles Bibliográficos
Autores principales: George, Jimmy, Khan, Hasan, Masood, Irfan, Akhtar, Zahra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9519499/
https://www.ncbi.nlm.nih.gov/pubmed/36189163
http://dx.doi.org/10.1016/j.radcr.2022.08.070
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author George, Jimmy
Khan, Hasan
Masood, Irfan
Akhtar, Zahra
author_facet George, Jimmy
Khan, Hasan
Masood, Irfan
Akhtar, Zahra
author_sort George, Jimmy
collection PubMed
description Amyloidosis is a rare condition on its own but finding localized amyloidosis of a site such as the nasopharynx is an extremely rare condition with very few cases described in the literature. The condition occurs due to the accumulation of misfolded proteins in the extracellular space disrupting the cell architecture and causing eventual dysfunction. In this case report we discuss the pathophysiology, symptoms, and imaging findings of a patient initially thought to have giant cell arteritis, but who was found on CT to have a mass later determined to be localized nasopharyngeal amyloidosis. Evaluation will require biopsy as it is the gold standard, but there are many other tests and even reasons to consider the use of interventional radiology to sample other tissues rather than the primary target site for amyloid deposition in conjunction with nuclear imaging.
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spelling pubmed-95194992022-09-30 Localized nasopharyngeal amyloidosis: A case report George, Jimmy Khan, Hasan Masood, Irfan Akhtar, Zahra Radiol Case Rep Case Report Amyloidosis is a rare condition on its own but finding localized amyloidosis of a site such as the nasopharynx is an extremely rare condition with very few cases described in the literature. The condition occurs due to the accumulation of misfolded proteins in the extracellular space disrupting the cell architecture and causing eventual dysfunction. In this case report we discuss the pathophysiology, symptoms, and imaging findings of a patient initially thought to have giant cell arteritis, but who was found on CT to have a mass later determined to be localized nasopharyngeal amyloidosis. Evaluation will require biopsy as it is the gold standard, but there are many other tests and even reasons to consider the use of interventional radiology to sample other tissues rather than the primary target site for amyloid deposition in conjunction with nuclear imaging. Elsevier 2022-09-26 /pmc/articles/PMC9519499/ /pubmed/36189163 http://dx.doi.org/10.1016/j.radcr.2022.08.070 Text en © 2022 The Authors. Published by Elsevier Inc. on behalf of University of Washington. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case Report
George, Jimmy
Khan, Hasan
Masood, Irfan
Akhtar, Zahra
Localized nasopharyngeal amyloidosis: A case report
title Localized nasopharyngeal amyloidosis: A case report
title_full Localized nasopharyngeal amyloidosis: A case report
title_fullStr Localized nasopharyngeal amyloidosis: A case report
title_full_unstemmed Localized nasopharyngeal amyloidosis: A case report
title_short Localized nasopharyngeal amyloidosis: A case report
title_sort localized nasopharyngeal amyloidosis: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9519499/
https://www.ncbi.nlm.nih.gov/pubmed/36189163
http://dx.doi.org/10.1016/j.radcr.2022.08.070
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