Results 21 to 30 of about 5,556 (167)

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

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

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

Cardiogenetics, 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, Emanuele Monda, Santo Dellegrottaglie, Annapaola Cirillo, Martina Caiazza, Adelaide Fusco, Francesca Esposito, Federica Verrillo, Giovanni Ciccarelli, Marta Rubino, Massimo Triggiani, Raffaele Scarpa, Alida Linda Patrizia Caforio, Renzo Marcolongo, Stefania Rizzo, Cristina Basso, Gerardo Nigro, Maria Giovanna Russo, Paolo Golino, Giuseppe Limongelli   +19 more
doaj   +1 more source

Renal Involvement in Eosinophilic Granulomatosis With Polyangiitis [PDF]

Kidney International Reports, 2021
Eosinophilic granulomatosis with polyangiitis (EGPA), previously called Churg-Strauss syndrome, is a small to medium-sized systemic necrotizing vasculitis characterized by eosinophil-rich tissue infiltrates and granulomatous lesions. EGPA belongs to the larger subgroup of ANCA-associated vasculitides (AAV).
Doreille, Alice, Buob, David, Bay, Pierre, Julien, Marie, Riviere, Frédéric, Rafat, Cédric   +5 more
openaire   +3 more sources

CLINICAL AND LABORATORY FEATURES OF ANCA ASSOCIATED VASCULITIS: EXPERIENCE AT A TERTIARY CARE HOSPITAL IN LAHORE, PAKISTAN

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, Asadullah kakkar, Haseeb Ahmed Khan, Saira Elaine Anwar khan   +3 more
doaj   +3 more sources

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

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

Oman 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, Aris Chandran Abdullah, Sin Fah Chung, Norain Karim, Jyi Jong Tang   +4 more
doaj   +1 more source

A rare case report of polyangiitis overlap syndrome: granulomatosis with polyangiitis and eosinophilic granulomatosis with polyangiitis

BMC Pulmonary Medicine, 2018
Background Granulomatosis with polyangiitis (GPA) is a systemic ANCA-associated vasculitis characterized by necrotizing granulomatous inflammation and a predilection for the upper and lower respiratory tract. Eosinophilic granulomatosis with polyangiitis
Michele V. Quan, Stephen K. Frankel, Mehrnaz Maleki-Fischbach, Laren D. Tan   +3 more
doaj   +1 more source