Bullous Vasculitis in Eosinophilic Granulomatosis with Polyangiitis: A Case Report
Introduction: Eosinophilic granulomatosis with polyangiitis (EGPA) is a rare systemic vasculitis affecting small- and medium-sized vessels. It is characterized by multiorgan involvement and can lead to severe outcomes if not diagnosed promptly. Cutaneous manifestations are common and typi...
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| Main Authors: | , |
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| Format: | Article |
| Language: | English |
| Published: |
Karger Publishers
2025-02-01
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| Series: | Case Reports in Dermatology |
| Online Access: | https://karger.com/article/doi/10.1159/000544815 |
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