Ocular Manifestations of Granulomatosis with Polyangiitis: A Review of the Literature

Granulomatosis with polyangiitis (GPA) is a rare systemic autoimmune disease of unknown etiology that is characterized by granulomatous inflammation, tissue necrosis, and vasculitis in small- and medium-sized vessels. Ocular and orbital manifestations are common in almost half of patients with GPA,...

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Detalles Bibliográficos
Autores principales: Sfiniadaki, Evdokia, Tsiara, Ioanna, Theodossiadis, Panagiotis, Chatziralli, Irini
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Healthcare 2019
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6513923/
https://www.ncbi.nlm.nih.gov/pubmed/30875067
http://dx.doi.org/10.1007/s40123-019-0176-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6513923/
https://www.ncbi.nlm.nih.gov/pubmed/30875067
http://dx.doi.org/10.1007/s40123-019-0176-8

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