Results 31 to 40 of about 9,401 (207)
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 +5 more
doaj +1 more source
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 +4 more
doaj +1 more source
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 +19 more
doaj +1 more source
Medial medullary infarction caused by antineutrophil cytoplasmic antibody-related vasculitis: Case report and review of the literature [PDF]
, 2017 Rationale: Medial medullary infarction accounts for less than 1% of brain infarctions, and medial medullary infarctions is very rarely caused by antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis.Patient concerns: We report the case of a 76-
Ishii Kazuhiro +7 more
core +2 more sources
Incidence of ANCA-associated vasculitis in a UK mixed ethnicity population [PDF]
, 2016 Objectives: We aimed to estimate the incidence of ANCA-associated vasculitis in the UK and how this varied by ethnic group. Methods: We identified incident cases of ANCA-associated vasculitis between March 2007 and June 2013 in the Nottingham–Derby ...
Alfred Mahr +10 more
core +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 +5 more
openaire +3 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 +11 more
core +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
Eosinophil granulomatosis polyangiitissel: esetbemutatások és irodalmi áttekintés [PDF]
, 2018 L
Herédi, Emese +4 more
core +1 more source
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 +3 more
doaj +3 more sources