Eosinophilic granulomatosis with polyangiitis coexisting with multiple myeloma: independent entities or coexistence? A case report

Eosinophilic granulomatosis with polyangiitis (EGPA) represents a systemic necrotizing vasculitis characterized by prominent peripheral eosinophilia. Concomitant plasma cell dyscrasias in the context of EGPA remain exceedingly rare in clinical literature. This paper presents a case of a 49-year-old...

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Autors principals:	Longyan Qin, Yi Yin, Pengjia Wu, Aifei Zhang, Na Li, Jun Liu, Ling Huang, Jun Cao, Jiashun Zeng
Format:	Artigo
Idioma:	Inglês
Publicat:	Frontiers Media S.A. 2026-03-01
Col·lecció:	Frontiers in Immunology
Matèries:	eosinophil eosinophilic granulomatosis with polyangiitis mepolizumab multiple myeloma plasma cell neoplasm
Accés en línia:	https://www.frontiersin.org/articles/10.3389/fimmu.2026.1751926/full
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