Results 41 to 50 of about 64,510,463 (206)

GPA-Induced Granulomatous Endocarditis Mimicking a Thrombotic Mitral Valve Stenosis

open access: yesJACC: Case Reports, 2020
We present the case of a patient with granulomatous endocarditis of the mitral valve leading to severe valve stenosis caused by granulomatosis with polyangiitis.
Christoph Marquetand, MD   +7 more
doaj   +1 more source

Granulomatosis with polyangiitis – therapeutic challenge

open access: yes, 2016
The antineutrophil cytoplasmic antibody (ANCA) associated vasculitides (AAV) are a group of primary vasculitides that affect predominantly small- to medium-sized blood vessels.
Małgorzata Wisłowska   +1 more
core   +1 more source

Pituitary involvement as a primary manifestation of granulomatosis with polyangiitis

open access: yes, 2022
Granulomatosis with polyangiitis is a systemic necrotizing granulomatous vasculitis that can predominantly affect systemic small- and medium-sized vessels.

core   +1 more source

Right atrial myxoma as the first manifestation of granulomatosis with polyangiitis, and a possible association with vascular endothelial growth factor (VEGF) and interleukin 6 (IL-6): a case report and review of the literature

open access: yesEuropean Journal of Medical Research, 2022
Background Granulomatosis with polyangiitis and myxomas are rare conditions previously described to co-exist. Cardiac masses are often presumed to be myxomas rather than lesions of granulomatosis with polyangiitis.
Joel Corin   +2 more
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

Granulomatosis with polyangiitis in a patient with polydipsia, facial nerve paralysis, and severe otologic complaints: a case report and review of the literature

open access: yesJournal of Medical Case Reports, 2022
Background Granulomatosis with polyangiitis, formerly known as Wegener granulomatosis, is a necrotizing vasculitis with granulomatous inflammation that belongs to the class of antineutrophil cytoplasmic antibodies-positive diseases.
Lukas Koenen   +4 more
doaj   +1 more source

Infectious complication or exacerbation of granulomatosis with polyangiitis?

open access: yes, 2015
Granulomatosis with polyangiitis (GPA) is a primary, systemic small vessel vasculitis. The respiratory tract is typically involved in the course of the disease.
Małgorzata Struk-Panfill   +2 more
core   +1 more source

Current and future prospects in the management of granulomatosis with polyangiitis (Wegener's granulomatosis) [PDF]

open access: yes, 2014
Ruth M Tarzi, Charles D PuseyRenal and Vascular Inflammation Section, Department of Medicine, Imperial College, London, UKAbstract: Granulomatosis with polyangiitis (GPA, formerly Wegener's granulomatosis) is a multisystem autoimmune condition ...
Pusey CD   +3 more
core   +1 more source

A Candidate Gene Approach to ANCA-Associated Vasculitis Reveals Links to the C3 and CTLA-4 Genes but not to the IL1-Ra And Fcγ-RIIa Genes

open access: yesKidney & Blood Pressure Research, 2013
Background/Aims: The aim of the study is to search for associations between Antineutrophil cytoplasm antibody (ANCA)-associated vasculitis (AAV) and polymorphisms in the genes of four key molecules possibly involved in different pathogenic pathways ...
Ulf Persson   +5 more
doaj   +1 more source

Race and Household Income Are Associated With Disease Outcomes in Pediatric Patients With Antineutrophil Cytoplasmic Antibody–Associated Vasculitis Hospitalized in the United States

open access: yesArthritis Care &Research, EarlyView.
Objective Race and household income impact outcomes in patients with rheumatic conditions; however, their role in pediatric antineutrophil cytoplasmic antibody (ANCA)–associated vasculitis (AAV) remains poorly understood. We aimed to evaluate whether race and ethnicity and household income are associated with severe AAV disease and renal outcomes among
Roberto Alejandro Valdovinos   +2 more
wiley   +1 more source

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