Multiple Cutaneous Manifestations in ANCA-Positive Eosinophilic Granulomatosis with Polyangiitis before and after Biologic Therapy: Clinical and Histopathologic Characterization of a Paradigmatic Case

Eosinophilic granulomatosis with polyangiitis (EGPA) is a rare immune-mediated vasculitis associated with anti-neutrophil cytoplasmic antibodies (ANCAs). Having systemic and possibly severe involvement, a prompt recognition of its clinical features is crucial to achieve favorable patient outcomes. A...

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Detalles Bibliográficos
Autores principales: Carnicelli, Giorgia, Sernicola, Alvise, Gomes, Vito, Cundari, Giulia, Trasarti, Stefania, Priori, Roberta, Grieco, Teresa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9782198/
https://www.ncbi.nlm.nih.gov/pubmed/36556045
http://dx.doi.org/10.3390/jcm11247429

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