Literature review and case study of recurrent EPGA with elevated IgG4 and positive HBsAg successfully treated with rituximab

Background Eosinophilic granulomatosis with polyangiitis (EGPA) is a rare form of autoimmune vasculitis. The involvement of IgG4 and HBsAg in EGPA is less common but can occur and may present unique challenges in management.Case presentation: We present a case study of a 70-year-old female diagnosed...

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Principais autores:	Junru Wang, Jun Wang, Nan Wang, Wei Wang, Ping Zhang, Yingying Lin, Guisen Li, Yurong Zou, Xiang Zhong
Formato:	Artigo
Idioma:	Inglês
Publicado em:	Taylor & Francis Group 2024-12-01
Colecção:	Renal Failure
Assuntos:	Eosinophilic granulomatosis with polyangiitis serum IgG4 steroids rituximab antineutrophil cytoplasmic antibody
Acesso em linha:	https://www.tandfonline.com/doi/10.1080/0886022X.2024.2390569
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