Results 31 to 40 of about 12,403 (234)

Eosinophilic granulomatosis with polyangiitis – Advances in pathogenesis, diagnosis, and treatment

Frontiers in Medicine, 2023
Eosinophilic granulomatosis with polyangiitis (EGPA) is a rare disease characterized by eosinophil-rich granulomatous inflammation and necrotizing vasculitis, pre-dominantly affecting small-to-medium-sized vessels.
J. Fijołek, E. Radzikowska
semanticscholar   +1 more source

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

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

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

A case of repetitive myocardial infarction with unobstructed coronaries due to Churg-Strauss syndrome [PDF]

, 2019
© The Author(s) 2019. Published by Oxford University Press on behalf of the European Society of Cardiology.BackgroundMyocardial infarction is most commonly caused by thrombosis occurring on a background of coronary atherosclerosis, resulting in reduced ...
Agewall, Benallegue, Dennert, Fatima, Grodzinsky, Groh, Lanham, Masi, Mukhtyar, Takagi, Tornvall, Trivedi   +11 more
core   +3 more sources

Eosinophil granulomatosis polyangiitissel: esetbemutatások és irodalmi áttekintés [PDF]

, 2018
L
Herédi, Emese, Remenyik, Éva, Sawhney, Irina, Szegedi, Andrea, Szántó, Antónia   +4 more
core   +1 more source

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

COVID-19 in a Patient Treated for Granulomatosis with Polyangiitis: Persistent Viral Shedding with No Cytokine Storm

European Journal of Case Reports in Internal Medicine, 2020
Introduction: The coronavirus disease COVID-19 is considered a pandemic disease that has developed rapidly all over the world. As of today, it is unclear whether immunosuppression confers an increased risk for pulmonary complications, or conversely ...
Pascale Daniel, Marc Raad, Rami Waked, Jacques Choucair, Moussa Riachy, Fady Haddad   +5 more
doaj   +1 more source

Eosinophilic granulomatosis with polyangiitis following flu guard influenza vaccination: A case report

Clinical Case Reports, 2023
Key Clinical Message This case highlights a potential association between influenza vaccination and the development of eosinophilic granulomatosis with polyangiitis (EGPA), prompting the need for increased vigilance regarding vaccine‐related autoimmune ...
Mehdi Jafarpour, Sara Daneshvar, Amir Taher Eftekharsadat, Alireza Khabbazi, Omid Pourbagherian   +4 more
doaj   +1 more source