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Granulomatous polyangiitis involving the fourth ventricle: Report of a rare case and a literature review

Granulomatous polyangiitis (GPA) is a rare systemic autoimmune vasculitis disease that is highly correlated with anti-neutrophil cytoplasmic antibodies (ANCAs). It was formerly called as “Wegener’s granulomatosis.” The clinical manifestations are diverse, mainly involving the upper respiratory tract...

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Detalles Bibliográficos
Autores principales: Yuan, Dan, Ji, Qing, Xia, Jin-Hua, Wang, Jin-Jing, Liang, Na
Formato: Online Artículo Texto
Lenguaje:English
Publicado: De Gruyter 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10358746/
https://www.ncbi.nlm.nih.gov/pubmed/37483427
http://dx.doi.org/10.1515/biol-2022-0654