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Pulmonary arteritis in the course of granulomatosis with polyangiitis. [PDF]
Sobuń A +5 more
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Comment on: Eosinophilic granulomatosis with polyangiitis across the eosinophilic spectrum: from molecular mechanisms to practical differential diagnosis and targeted therapy. [PDF]
Kosałka-Węgiel J, Korkosz M.
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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 ...
Yann Nguyen, Loïc Guillevin
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Granulomatosis with polyangiitis
Journal of Clinical Images and Medical Case Reports, 2023A 30 year old male presented to the emergency department with a 6 month history of hemoptysis and epistaxis. He was otherwise healthy with no known medical conditions, no prior surgery, and was taking no medications. His vital signs were normal and his oxygen saturation was 99% SaO2 on room air.
Dilek Karadoğan +2 more
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Granulomatosis with Polyangiitis (Wegener’s Granulomatosis)
2014Granulomatosis with polyangiitis (formerly, Wegener’s granulomatosis) is a systemic necrotizing and granulomatous vasculitis predominantly affecting small-sized vessels. It is also one of the three vasculitides associated with anti-neutrophil cytoplasm antibodies (ANCA).
Susanne Schinke +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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