Results 1 to 10 of about 64,510,463 (206)
An overlap of granulomatosis with polyangiitis and eosinophilic granulomatosis with polyangiitis
Saudi Journal of Kidney Diseases and Transplantation, 2017 We present a case report of overlap of granulomatosis with polyangiitis (GPA; formerly known as Wegener’s granulomatosis) and eosinophilic granulomatosis with polyangiitis (EGPA; formerly known as Churg-Strauss syndrome).
Sujit Surendran +4 more
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A rare case report of polyangiitis overlap syndrome: granulomatosis with polyangiitis and eosinophilic granulomatosis with polyangiitis [PDF]
BMC Pulmonary Medicine, 2018 Background Granulomatosis with polyangiitis (GPA) is a systemic ANCA-associated vasculitis characterized by necrotizing granulomatous inflammation and a predilection for the upper and lower respiratory tract. Eosinophilic granulomatosis with polyangiitis
Michele V. Quan +3 more
doaj +4 more sources
Granulomatosis with polyangiitis [PDF]
Bangabandhu Sheikh Mujib Medical University Journal, 2016 Granulomatosis with polyangiitis is a small and medium vessel vasculitis. It may affect any organ system. Neurological involvement, though less frequent, mostly manifests as peripheral neuropathy.
Zubayer Ahmad +4 more
doaj +5 more sources
Granulomatosis with polyangiitis [PDF]
Jornal Brasileiro de PneumologiaA 30-year-old man presented to otolaryngology department complaining of nasal congestion and runny nose for six months, with repeated fever, and shortness of breath.The weight loss in the past 20 days was about 5 kg.
Roberta Wartchow Machado +2 more
doaj +12 more sources
Eosinophilic granulomatosis with polyangiitis
Postgraduate Medicine, 2022 This review aims to describe the epidemiology, pathogenesis, clinical manifestations, diagnosis, treatment, and prognosis of eosinophilic granulomatosis with polyangiitis (EGPA). Eosinophilic granulomatosis with polyangiitis is a small to medium vessel necrotizing vasculitis, typically classified with granulomatosis with polyangiitis (GPA) and ...
Geng-Yi Yong, Amelia L.-S. Lim
core +9 more sources
Granulomatosis with polyangiitis: A case report and brief review of literature
Radiology Case Reports, 2021 : Granulomatosis with polyangiitis formerly known as Wegener's granulomatosis was first described by German pathologist Friedrich Wegener in 1936. It is a multi-system necrotizing noncaseating granulomatous vasculitis which affects small to medium-sized ...
Kelly Smith +2 more
exaly +3 more sources
Eosinophilic Granulomatosis with Polyangiitis: An Overview [PDF]
Frontiers in Immunology, 2014 Eosinophilic granulomatosis with polyangiitis (EGPA) is a multisystemic disorder, belonging to the small vessel anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis, defined as an eosinophil-rich and necrotizing granulomatous inflammation often involving the respiratory tract, and necrotizing vasculitis predominantly affecting small to ...
Carlo Buzio
exaly +4 more sources
Granulomatosis with Polyangiitis [PDF]
Clinical Medicine (Russian Journal), 2020 Granulomatosis with polyangiitis is a form of granulomatous vasculitis that affects small- and medium-sized vessels in many organs but most commonly affects the upper respiratory tract and the kidneys. Ocular disease can be the presenting or even the only clinically apparent manifestation; it can involve any part of the eye.
S. A. Shchekina +2 more
+8 more sources
A clinical case of lung damage in granulomatosis with polyangiitis
Бюллетень сибирской медицины, 2021 The article presents a case of granulomatosis with polyangiitis, which is difficult for clinical diagnosis. Recently, the incidence of systemic vasculitis has increased, and given the similarity of clinical symptoms with other pathologies, a doctor of ...
A. Yu. Kraposhina +9 more
doaj +1 more source
Journal of Medical Internet Research, 2020 BackgroundUtilizing the traditional centers of excellence approach to conduct clinical trials involving rare diseases remains challenging.
Springer, Jason Michael +6 more
doaj +1 more source