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An Atypical Presentation of Polyarteritis Nodosa: Case Report and Review of the Literature

Polyarteritis nodosa (PAN) is a rare multisystem vasculopathy that predominantly affects medium-sized arteries. Involvement of the cardiac and/or pulmonary vasculature may be fatal. We describe a 67-year-old Japanese male who presented with multiple coronary artery aneurysms and subsequently develop...

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Autores principales: Boppana, Sri Harsha, Dulla, Nageswara R, Beutler, Bryce D, Pitani, Sujatha, Kaur, Ratinder
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8085364/
https://www.ncbi.nlm.nih.gov/pubmed/33936904
http://dx.doi.org/10.7759/cureus.14197
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author Boppana, Sri Harsha
Dulla, Nageswara R
Beutler, Bryce D
Pitani, Sujatha
Kaur, Ratinder
author_facet Boppana, Sri Harsha
Dulla, Nageswara R
Beutler, Bryce D
Pitani, Sujatha
Kaur, Ratinder
author_sort Boppana, Sri Harsha
collection PubMed
description Polyarteritis nodosa (PAN) is a rare multisystem vasculopathy that predominantly affects medium-sized arteries. Involvement of the cardiac and/or pulmonary vasculature may be fatal. We describe a 67-year-old Japanese male who presented with multiple coronary artery aneurysms and subsequently developed lower extremity gangrene. A diagnosis of PAN was established based on the correlation of clinical presentation and laboratory and imaging findings. In addition, we review other manifestations of PAN and differential considerations for this rare but potentially lethal condition.
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spelling pubmed-80853642021-04-30 An Atypical Presentation of Polyarteritis Nodosa: Case Report and Review of the Literature Boppana, Sri Harsha Dulla, Nageswara R Beutler, Bryce D Pitani, Sujatha Kaur, Ratinder Cureus Internal Medicine Polyarteritis nodosa (PAN) is a rare multisystem vasculopathy that predominantly affects medium-sized arteries. Involvement of the cardiac and/or pulmonary vasculature may be fatal. We describe a 67-year-old Japanese male who presented with multiple coronary artery aneurysms and subsequently developed lower extremity gangrene. A diagnosis of PAN was established based on the correlation of clinical presentation and laboratory and imaging findings. In addition, we review other manifestations of PAN and differential considerations for this rare but potentially lethal condition. Cureus 2021-03-30 /pmc/articles/PMC8085364/ /pubmed/33936904 http://dx.doi.org/10.7759/cureus.14197 Text en Copyright © 2021, Boppana et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Internal Medicine
Boppana, Sri Harsha
Dulla, Nageswara R
Beutler, Bryce D
Pitani, Sujatha
Kaur, Ratinder
An Atypical Presentation of Polyarteritis Nodosa: Case Report and Review of the Literature
title An Atypical Presentation of Polyarteritis Nodosa: Case Report and Review of the Literature
title_full An Atypical Presentation of Polyarteritis Nodosa: Case Report and Review of the Literature
title_fullStr An Atypical Presentation of Polyarteritis Nodosa: Case Report and Review of the Literature
title_full_unstemmed An Atypical Presentation of Polyarteritis Nodosa: Case Report and Review of the Literature
title_short An Atypical Presentation of Polyarteritis Nodosa: Case Report and Review of the Literature
title_sort atypical presentation of polyarteritis nodosa: case report and review of the literature
topic Internal Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8085364/
https://www.ncbi.nlm.nih.gov/pubmed/33936904
http://dx.doi.org/10.7759/cureus.14197
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