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Treatment Approaches to Granulomatosis With Polyangiitis and Microscopic Polyangiitis
Rheumatic Disease Clinics of North America, 2023 We have made significant headway in our ability to induce and maintain remission in patients with granulomatosis with polyangiitis and microscopic polyangiitis. With increased understanding of the pathogenesis of antineutrophilic cytoplasmic antibody-associated vasculitides (AAV), therapeutic targets have been identified and studied in clinical trials.
Alvise Berti, Divi Cornec
exaly +6 more sources
Microscopic Polyangiitis [PDF]
Rheumatic Disease Clinics of North America, 2010 In 1923, Friedrich Wohlwill described two patients with a "microscopic form of periarteritis nodosa," which was distinct from the classical form. This disease, now known as microscopic polyangiitis (MPA), is a primary systemic vasculitis characterized by inflammation of the small-caliber blood vessels and the presence of circulating antineutrophil ...
Philip Seo, Sharon Chung
exaly +6 more sources
Temporal Arteritis and Vision Loss in Microscopic Polyangiitis: A Case Report and Literature Review
Case Reports in Nephrology, 2020 Microscopic polyangiitis (MPA) is an idiopathic autoimmune disease characterized by systemic vasculitis. While the lungs and kidneys are the major organs affected by MPA, it is known to involve multiple organ systems throughout the body.
Alexander G. Goglia +3 more
doaj +2 more sources
Acta Médica del Centro, 2012 A white elderly patient, with a history of hypertension, gout and type 2 diabetes mellitus was admitted with severe cough, dyspnea, marked asthenia and hematemesis.
Noel Ernesto Pedraza Alonso +11 more
doaj +3 more sources
Microscopic polyangiitis [PDF]
Arkhiv patologii, 2020 The paper describes an autopsy case of a 69-year-old woman with microscopic polyangiitis lasting about 1.5 months despite intensive treatment. She had generalized productive vasculitis, extracapillary productive glomerulonephritis, adult respiratory distress syndrome with focal pneumonia, isolated lung atelectasis, splenic infarction, and toe and ...
E A, Kogan +3 more
+7 more sources
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
Pakistan Armed Forces Medical Journal, 2021 Objective: To determine the clinical and laboratory features during the disease course in patients of anti cytoplasmic antibody (ANCA) associated vasculitis in Pakistani patients presenting to a tertiary care center.
Muhammad Zeeshan Aslam +3 more
doaj +3 more sources
Frontiers in Medicine, 2022 Antineutrophil cytoplasmic antibody associated vasculitis includes granulomatosis with polyangiitis, eosinophilic granulomatosis with polyangiitis (EGPA), and microscopic polyangiitis.
Lirong Lin +4 more
doaj +1 more source
Clinical Case Reports, 2021 Although extra‐glomerular involvement of microscopic polyangiitis is not regarded as a characteristic finding of the disease, tubulointerstitial nephritis should be considered as a new subclass of renal involvement.
Se Hee Kim +3 more
doaj +1 more source
Clinical features of kidney involvement in microscopic microscopic polyangiitis [PDF]
Терапевтический архив, 2018 Aim. To evaluate clinical features and outcomes of renal involvement in patients with microscopic polyangiitis (MPA). Materials and methods: We enrolled 99 patients with MPA, diagnosed in accordance with the algorithm of the European Medicines Evaluation
E M Shchegoleva +3 more
doaj +1 more source