An autopsy case of myeloperoxidase-anti-neutrophil cytoplasmic antibody (MPO-ANCA)-associated vasculitis accompanied by cryoglobulinemic vasculitis affecting the kidneys, skin, and gastrointestinal tract

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Abstract

Anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) and cryoglobulinemic vasculitis (CV) rarely coexist. An 83-year-old woman was admitted with rapidly progressive renal failure, gastrointestinal hemorrhage and purpura with myeloperoxidase (MPO)-ANCA positivity and cryoglobulinemia. Despite intensive immunosuppressive treatment, she died of aspergillus pneumonia. Autopsy revealed necrotizing crescentic glomerulitis in the majority of the glomeruli, accompanied by partially membranoproliferative-like glomerular changes. Immunofluorescence staining revealed the presence of neutrophil extracellular trap (NET) formation in the glomeruli and cutaneous arteries. These pathological findings suggested that MPO-AAV and/or CV caused NET formation, leading to lethal systemic vasculitis.

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Hasegawa, J., Wakai, S., Kono, M., Imaizumi, Y., Masuda, S., Ishizu, A., & Honda, K. (2018). An autopsy case of myeloperoxidase-anti-neutrophil cytoplasmic antibody (MPO-ANCA)-associated vasculitis accompanied by cryoglobulinemic vasculitis affecting the kidneys, skin, and gastrointestinal tract. Internal Medicine, 57(18), 2739–2745. https://doi.org/10.2169/internalmedicine.0720-17

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