Results 21 to 30 of about 9,401 (207)

Eosinophilic Granulomatosis With Polyangiitis Presenting With Oral Granuloma as the Initial Symptom: A Case Report

Frontiers in Medicine, 2022
Antineutrophil cytoplasmic antibody associated vasculitis includes granulomatosis with polyangiitis, eosinophilic granulomatosis with polyangiitis (EGPA), and microscopic polyangiitis.
Lirong Lin, Rongjie Yu, Luquan Zheng, Shuyu Gong, Jurong Yang   +4 more
doaj   +1 more source

An atypical presentation of cardiac tamponade and periorbital swelling in a patient with eosinophilic granulomatosis with polyangiitis: a case report

Journal of Medical Case Reports, 2017
Background Eosinophilic granulomatosis with polyangiitis is a rare, necrotizing systemic vasculitis associated with asthma and hypereosinophilia. Its cause and pathophysiology are still being elucidated. Case presentation We report a case of eosinophilic
Alexandra C. Keefe, Joseph C. Hymas, Lyska L. Emerson, John J. Ryan   +3 more
doaj   +1 more source

Eosinophilic granulomatosis with polyangiitis (EGPA) and PRES: a case-based review of literature in ANCA-associated vasculitides [PDF]

, 2015
Eosinophilic granulomatosis with polyangiitis (EGPA) is a small-sized vessel systemic necrotizing vasculitis and belongs to the family of antineutrophil cytoplasmic antibody (ANCA)-associated vasculitides.
Barilaro, Giuseppe, Granata, Massimo, Marra, ALESSANDRO MARIA, Villella, Valeria   +3 more
core   +1 more source

T Cells in Vascular Inflammatory Diseases [PDF]

, 2014
Inflammation of the human vasculature is a manifestation of many different diseases ranging from systemic autoimmune diseases to chronic inflammatory diseases, in which multiple types of immune cells are involved. For both autoimmune diseases and chronic
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core   +7 more sources

An uncommon presentation of eosinophilic granulomatosis with polyangiitis: a case report [PDF]

, 2014
INTRODUCTION: Eosinophilic granulomatosis with polyangiitis is a rare and potentially fatal disease if not readily diagnosed. Cerebral involvement is extremely rare and clinical presentation as hemorrhagic stroke is even rarer.
Andolina, G, Banco, MA, Bonura, A, BUSCEMI, Silvio, COSTANZA GAGLIO, Edy, TAORMINA, Giuseppe   +5 more
core   +2 more sources

ANCA-associated vasculitis [PDF]

, 2017
The vasculitides are a heterogeneous group of conditions typified by their ability to cause vessel inflammation with or without necrosis. They present with a wide variety of signs and symptoms and, if left untreated, carry a significant burden of ...
Watts, Richard, Yates, Max
core   +1 more source

Severe mononeuritis multiplex in a patient with eosinophilic granulomatosis with polyangiitis

Rheumatology, 2019
Eosinophilic granulomatosis with polyangiitis (EGPA) is a systemic vasculitis characterised by bronchial asthma, hypereosinophilia, and systemic vasculitis.
Desislava Kalinova, Georgi Kukushev, Zlatimir Kolarov, Rasho Rashkov   +3 more
doaj   +1 more source

Eosinophilic granulomatosis with polyangiitis

, 2019
26 years ...
Vincent Cottin, Kais Ahmad, Mouhamad Nasser, Claudia Valenzuela, Matthieu Groh, Benjamin Terrier, Julie Traclet   +6 more
  +4 more sources

ANCA Associated Mononeuritis Multiplex with Overlap in Vasculitic Syndromes [PDF]

Journal of Clinical and Diagnostic Research, 2017
Mononeuritis multiplex is a common manifestation of many illnesses which includes Hansen’s disease and certain types of systemic vasculitis. The Antineutrophil Cytoplasmic Antibody (ANCA)-Associated Vasculitis (AAV) is a group of rare diseases which ...
Ravi Anadure, Coimbatore Narayanan, Govindraj Varadraj, Bevinahalli Nandeesh   +3 more
doaj   +1 more source

Review of guideline for the management of ANCA-associated vasculitis, presented in 2021 by the American College of Rheumatology/Vasculitis Foundation

Научно-практическая ревматология, 2021
The anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitides (AAVs) are a group of severe life-threatening autoimmune diseases, and one of the most important problems in practical rheumatology.
T. V. Beketova, I. Yu. Popov, V. V. Babak   +2 more
doaj   +1 more source