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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...
Autores principales: | Yuan, Dan, Ji, Qing, Xia, Jin-Hua, Wang, Jin-Jing, Liang, Na |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
De Gruyter
2023
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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 |
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