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Localized mediastinal amyloidosis: A misnomer?

Amyloidosis is a disease related to abnormal protein folding and deposition of that abnormal protein between cells of the body in various tissues and organs, resulting in multiple clinical manifestations. We report a case of amyloidosis with atypical features, isolated to the mediastinum, in a 75-ye...

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Detalles Bibliográficos
Autores principales: Hoch, Michael, Wang, Congli, Caroline, Dina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4899862/
https://www.ncbi.nlm.nih.gov/pubmed/27326282
http://dx.doi.org/10.2484/rcr.v7i2.647
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author Hoch, Michael
Wang, Congli
Caroline, Dina
author_facet Hoch, Michael
Wang, Congli
Caroline, Dina
author_sort Hoch, Michael
collection PubMed
description Amyloidosis is a disease related to abnormal protein folding and deposition of that abnormal protein between cells of the body in various tissues and organs, resulting in multiple clinical manifestations. We report a case of amyloidosis with atypical features, isolated to the mediastinum, in a 75-year-old male who presented with fatigue and shortness of breath. Amyloidosis that is isolated to the mediastinum without pulmonary parenchymal involvement is exceptionally rare. It has been hypothesized that localized mediastinal amyloidosis manifesting as amyloidomas is a distinct clinical subtype with a better prognosis than classic systemic amyloidosis. This paper describes the radiologic features of localized mediastinal amyloidosis (along with its pathologic correlation) and compares systemic and isolated disease.
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spelling pubmed-48998622016-06-20 Localized mediastinal amyloidosis: A misnomer? Hoch, Michael Wang, Congli Caroline, Dina Radiol Case Rep Article Amyloidosis is a disease related to abnormal protein folding and deposition of that abnormal protein between cells of the body in various tissues and organs, resulting in multiple clinical manifestations. We report a case of amyloidosis with atypical features, isolated to the mediastinum, in a 75-year-old male who presented with fatigue and shortness of breath. Amyloidosis that is isolated to the mediastinum without pulmonary parenchymal involvement is exceptionally rare. It has been hypothesized that localized mediastinal amyloidosis manifesting as amyloidomas is a distinct clinical subtype with a better prognosis than classic systemic amyloidosis. This paper describes the radiologic features of localized mediastinal amyloidosis (along with its pathologic correlation) and compares systemic and isolated disease. Elsevier 2015-12-07 /pmc/articles/PMC4899862/ /pubmed/27326282 http://dx.doi.org/10.2484/rcr.v7i2.647 Text en © 2012 The Authors. http://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 Article
Hoch, Michael
Wang, Congli
Caroline, Dina
Localized mediastinal amyloidosis: A misnomer?
title Localized mediastinal amyloidosis: A misnomer?
title_full Localized mediastinal amyloidosis: A misnomer?
title_fullStr Localized mediastinal amyloidosis: A misnomer?
title_full_unstemmed Localized mediastinal amyloidosis: A misnomer?
title_short Localized mediastinal amyloidosis: A misnomer?
title_sort localized mediastinal amyloidosis: a misnomer?
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4899862/
https://www.ncbi.nlm.nih.gov/pubmed/27326282
http://dx.doi.org/10.2484/rcr.v7i2.647
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