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2020•Clinical Journal of the American Society of NephrologyOpen access

Treatment of Granulomatosis with Polyangiitis and Microscopic Polyangiitis

Vladimı́r Tesař, Zdenka Hrušková

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Abstract

Granulomatosis with polyangiitis (GPA) and microscopic polyangiitis (MPA) are two major clinical entities recognized among ANCA-associated vasculitides. GPA and MPA differ in the presence or absence of granuloma, organ involvement, and risk of relapses. GPA is more often, but not exclusively,

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What this paper is about

Granulomatosis with polyangiitis (GPA) and microscopic polyangiitis (MPA) are two major clinical entities recognized among ANCA-associated vasculitides. GPA and MPA differ in the presence or absence of granuloma, organ involvement, and risk of relapses. GPA is more often, but not exclusively,

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Available abstract

Granulomatosis with polyangiitis (GPA) and microscopic polyangiitis (MPA) are two major clinical entities recognized among ANCA-associated vasculitides. GPA and MPA differ in the presence or absence of granuloma, organ involvement, and risk of relapses. GPA is more often, but not exclusively,

Key concepts: Granulomatosis with polyangiitis, Microscopic polyangiitis, Medicine, Granuloma formation, Wegener granulomatosis, Vasculitis, Granuloma, Dermatology

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