Results 171 to 180 of about 64,510,463 (206)

Diagnosis and classification of granulomatosis with polyangiitis (aka Wegener's granulomatosis)

open access: yesJournal of Autoimmunity, 2014
Granulomatosis with polyangiitis (GPA, formerly known as Wegener's Granulomatosis) is an autoimmune small vessel vasculitis which is highly associated with anti-neutrophil cytoplasmic antibodies (ANCA).
David D'Cruz
exaly   +2 more sources

Eosinophilic granulomatosis with polyangiitis

Medicina Clínica (English Edition), 2023
Eosinophilic granulomatosis with polyangiitis (EGPA) is a systemic vasculitis characterized by the presence of asthma associated with eosinophilia, eosinophilic infiltration of different organs, and vasculitis of small and medium-sized vessels. Although classified as anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis, it occurs in less ...
Carlos, Romero Gómez   +2 more
openaire   +3 more sources

Granulomatosis with Polyangiitis in Childhood

Current Rheumatology Reports, 2012
Granulomatosis with polyangiitis (GPA) is a rare yet frequently organ- or life-threatening systemic vasculitis affecting small- to medium-sized arteries in multiple organs. It characteristically leads to alveolar hemorrhage and destructive, pauci-immune glomerulonephritis. GPA is also characterized by granulomas in the upper and lower respiratory tract
Marinka, Twilt   +2 more
openaire   +2 more sources

Granulomatosis with polyangiitis (Wegener's)

Joint Bone Spine, 2020
Granulomatosis with polyangiitis (GPA) (Wegener) is a necrotizing vasculitis combining inflammation of the vascular wall and peri- and extravascular granulomatosis. Clinically, GPA is characterized in its full form by ENT signs, lung, and kidney involvement.
openaire   +2 more sources

Granulomatosis with polyangiitis

Oral Surgery, 2014
AbstractGranulomatosis with polyangiitis (GPA), which was formerly known as Wegener's granulomatosis, is a rare systemic condition with oral manifestations. This case report describes and discusses the oral presentation, investigations, diagnosis and management options in a patient who was diagnosed with GPA.
P. Hoyle, J.C. Steele
openaire   +1 more source

Eosinophilic Granulomatosis With Polyangiitis

JAMA Dermatology, 2021
Abraham M, Korman, Catherine G, Chung
openaire   +2 more sources

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