Results 21 to 30 of about 67,511,782 (172)

Eosinophilic granulomatosis with polyangiitis-related myocarditis during mepolizumab therapy reveals a Th1/Th17-mediated vasculitic response

open access: yes, 2021
Eosinophilic granulomatosis with polyangiitis-related myocarditis during mepolizumab therapy reveals a Th1/Th17-mediated vasculitic ...
Annunziato, Francesco   +13 more
core   +1 more source

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

open access: yesJournal 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   +3 more
doaj   +1 more source

Pancarditis as the Clinical Presentation of Eosinophilic Granulomatosis with Polyangiitis: A Multimodality Approach to Diagnosis

open access: yesCardiogenetics, 2022
Eosinophilic pancarditis (EP) is a rare, often unrecognized condition caused by endomyocardial infiltration of eosinophil granulocytes (referred as eosinophilic myocarditis, EM) associated with pericardial involvement.
Michele Lioncino   +19 more
doaj   +1 more source

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

open access: yesClinical 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   +4 more
doaj   +1 more source

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

open access: yesEuropean 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   +5 more
doaj   +1 more source

Early benralizumab for eosinophilic myocarditis in eosinophilic granulomatosis with polyangiitis [PDF]

open access: yes, 2020
Eosinophilic myocarditis is a life-threatening complication of eosinophilic syndromes including eosinophilic granulomatosis with polyangiitis (EGPA), undefined complex hypereosinophilic syndrome (HES), and drug rash with eosinophilia and systemic ...
Colantuono, Stefania   +5 more
core   +1 more source

International guidelines for the management ofANCA-associated systemic vasculitides

open access: yesСовременная ревматология, 2019
The paper deals with international guidelines for the management of antineutrophil cytoplasmic antibody (ANCA)-associated systemic vasculitides (SVs) that are a group of severe life-threatening immune-mediated diseases. This group includes granulomatosis
T. V. Beketova
doaj   +1 more source

Acute heart failure with left ventricular thrombus in the course of eosinophilic granulomatosis with polyangiitis [PDF]

open access: yes, 2014
Eosinophilic granulomatosis with polyangiitis (EGPA) characterized by the coexistence of asthma, eosinophilia and characteristic histopathologic changes, is one of the primary systemic small vessel inflammation of unknown etiology. Cardiac involvement in
Żaneta Smoleńska   +3 more
core   +1 more source

Mepolizumab for Eosinophilic Granulomatosis with Polyangiitis (EGPA): a European multicenter observational study [PDF]

open access: yes, 2021
Mepolizumab proved efficacious for eosinophilic granulomatosis with polyangiitis (EGPA, former Churg-Strauss) at the dosage of 300mg/4 weeks in the randomized controlled MIRRA trial.
Lombardi, Carlo   +328 more
core   +4 more sources

Cutaneous Vasculitis as Early Presentation of Eosinophilic Granulomatosis with Polyangiitis without Systemic Symptoms

open access: yesOman Medical Journal, 2019
Eosinophilic granulomatosis with polyangiitis (formerly known as Churg-Strauss syndrome) is a rare vasculitis in children. It commonly presents with respiratory symptoms, especially asthma, allergic rhinitis, and peripheral eosinophilia.
Wahinuddin Sulaiman   +4 more
doaj   +1 more source

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