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Current management of eosinophilic granulomatosis with polyangiitis across Europe: insights from a multinational expert survey. [PDF]

Rheumatology (Oxford)
Conticini E, Emmi G, Grazzini S, André M, Cohen Tervaert JW, Durante E, Torracca F, Mohammad AJ, Moosig F, Neumann T, Solans Laque R, Terrier B, Vaglio A, Cameli P, European EGPA Study Group (EESG).   +14 more
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Correction to "Kimura Disease With Eosinophilic Granulomatosis With Polyangiitis Successfully Treated by Mepolizumab". [PDF]

Clin Case Rep
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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, Halbert, Hernández Negrín, María Del Mar, Ayala Gutiérrez   +2 more
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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, Susanne, Benseler, David, Cabral   +2 more
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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.
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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
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Eosinophilic Granulomatosis With Polyangiitis

JAMA Dermatology, 2021
Abraham M, Korman, Catherine G, Chung
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Granulomatosis with Polyangiitis

2018
Granulomatosis with polyangiitis (GPA), formerly Wegener’s granulomatosis, is a systemic vasculitis of unknown etiology affecting both small- and medium-sized arteries and veins. GPA manifests as necrotizing granulomatous inflammation in the lungs, kidneys, upper respiratory tract, nerves, and rarely heart.
J. Murphy, J. Ross, L. Coleman, M. Zakowski   +3 more
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