Myocarditis due to eosinophilic granulomatosis with polyangiitis: Case report and literature review

Eosinophilic Granulomatosis with Polyangiitis (EGPA) is a rare systemic vasculitis, with cardiac involvement being one of its most severe and life-threatening complications.

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Publication Details

Journal
Journal of Clinical Images and Medical Case Reports
Published
2025-04-15
DOI
https://doi.org/10.52768/2766-7820/3553
Primary Topic
Eosinophilic Disorders and Syndromes
Type
article
Field-Weighted Citation Impact
0.00
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article

Myocarditis due to eosinophilic granulomatosis with polyangiitis: Case report and literature review

Luzia Hermínia Teixeira de Sousa
Journal of Clinical Images and Medical Case Reports
Eosinophilic Disorders and Syndromes
article

Myocarditis due to eosinophilic granulomatosis with polyangiitis: Case report and literature review

Luzia Hermínia Teixeira de Sousa
article en

Abstract

Eosinophilic Granulomatosis with Polyangiitis (EGPA) is a rare systemic vasculitis, with cardiac involvement being one of its most severe and life-threatening complications.

Journal of Clinical Images and Medical Case ReportsVol. 6(4)
Openalex Percentile: Top 71%
Eosinophilic Disorders and Syndromes
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Myocarditis due to eosinophilic granulomatosis with polyangiitis: Case report and literature review — Luzia Hermínia Teixeira de Sousa · Journal of Clinical Images and Medical Case Reports (2025) | TGRS Research Map | TGRS