Results 31 to 40 of about 64,509,941 (193)

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

, 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, Anna Masiak, Zenobia Czuszyńska, Zbigniew Zdrojewski   +3 more
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

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

, 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, Pellicano, Chiara, Cilia, Francesco, Francone, Marco, Leodori, Giorgia, Visentini, Marcella   +5 more
core   +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

Sequential rituximab and mepolizumab in eosinophilic granulomatosis with polyangiitis (EGPA): a European multicentre observational study [PDF]

, 2022
Sequential rituximab and mepolizumab in eosinophilic granulomatosis with polyangiitis (EGPA): a European multicentre observational ...
Flossmann, Oliver, Marc André, Maria Letizia Urban, Jayne, David, Bettiol, Alessandra, Egan, A., Emmi, G., Irene Mattioli, Vaglio, Augusto, Prisco, Domenico, Fiori, Davide, Jan Schroeder, Padoan, Roberto, Dagna, Lorenzo, Iannone, Florenzo, Egan, Allyson, Giacomo Emmi, André, M., Franceschini, Franco, Vaglio, A., Florenzo Iannone, Negrini, S., Schroeder, J., David Jayne, Franceschini, F., Allyson Egan, Urban, Maria Letizia, Franco Franceschini, Oliver Flossmann, Dagna, L., Federica Bello, Bargagli, E., Moi, L., Silvestri, Elena, Emmi, Giacomo, Roberto Padoan, Laura Moi, Domenico Prisco, Sciascia, Savino, Caminati, M., Sciascia, S., Paola Parronchi, Prisco, D., André, Marc, Lorenzo Dagna, Padoan, R., Fiori, D., Marco Caminati, Bello, F., Solans, R., Jayne, D., Negrini, Simone, Alessandra Bettiol, Simone Negrini, Giuseppe Lopalco, Dario Roccatello, Urban, M.L., Moi, Laura, Bettiol, A., Parronchi, P., Caminati, Marco, Schroeder, Jan, Roser Solans, Bargagli, Elena, Davide Fiori, Mattioli, Irene, Mattioli, I., Bello, Federica, Augusto Vaglio, Lopalco, Giuseppe, Iannone, F., Flossmann, O., Folci, Marco, Elena Bargagli, Roccatello, D., Roccatello, Dario, Savino Sciascia, Parronchi, Paola, Marco Folci, Folci, M., Solans, Roser, Lopalco, G.   +81 more
core   +1 more source

Development of eosinophilic granulomatosis with polyangiitis during the clinical course of microscopic polyangiitis: A case report [PDF]

, 2022
Rationale: Eosinophilic granulomatosis with polyangiitis (EGPA) is belongs to the antineutrophil cytoplasmic autoantibody (ANCA)-associated vasculitis (AAV) subgroups.
Shigematsu, Kazuto, Kojima, Kanako, Koike, Yuta, Kawakami, Atsushi, Shimizu, Toshimasa, Abe, Kuniko, Yuta Koike, Kazuto Shigematsu, Shinya Nishihata, Kuniko Abe, Kanako Kojima, Atsushi Kawakami, Nishihata, Shinya, Hiroyuki Ide, Ichinose, Kunihiro, Toshimasa Shimizu, Ide, Hiroyuki, Kunihiro Ichinose   +17 more
core   +2 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

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

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

International guidelines for the management ofANCA-associated systemic vasculitides

Современная 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