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- W2316985190 abstract "Granulomatosis with polyangiitis (GPA) is a chronic systemic disease that is characterized by granulomatous inflammation of the upper and lower respiratory tract accompanied by systemic vasculitis of small and medium-sized vessels and necrotizing glomerulonephritis. The etiology is unknown and it is more common in men. GPA is diagnosed with the clinical findings, positive antineutrophil cytoplasmic antibody (c-ANCA), and histological findings. Eye involvement is frequent but retinal vasculitis has rarely been described. Herein we will present a 76-year-old female patient with a GPA diagnosis who was on routine hemodialysis because of renal failure and developed retinal vein occlusion during the clinical follow-up. Key wORDS: Granulomatosis with polyangiitis, Retinal vasculitis, Glomerulonephritis" @default.
- W2316985190 created "2016-06-24" @default.
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- W2316985190 date "2016-03-17" @default.
- W2316985190 modified "2023-09-26" @default.
- W2316985190 title "A Case of Granulomatosis with Polyangiitis Relapse with Eye Involvement Only" @default.
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- W2316985190 doi "https://doi.org/10.5262/tndt.2016.39" @default.
- W2316985190 hasPublicationYear "2016" @default.
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