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Eosinophilic granulomatosis with polyangiitis
Medicina Clínica (English Edition), 2023Eosinophilic 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
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Granulomatosis with Polyangiitis in Childhood
Current Rheumatology Reports, 2012Granulomatosis 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
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Granulomatosis with polyangiitis (Wegener's)
Joint Bone Spine, 2020Granulomatosis 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, 2014AbstractGranulomatosis 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, 2021Abraham M, Korman, Catherine G, Chung
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Granulomatosis with Polyangiitis
La Revue du praticien, 2021George N. Papaliodis, Caroline L. Minkus
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Sclerokeratitis in Granulomatosis with Polyangiitis
New England Journal of Medicine, 2022Abigail, Jebaraj, Amy, Lin
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