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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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Detalles Bibliográficos
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
Descripción
Sumario: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.