Systemic vasculitis - Open Access .click

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Autoantibodies in systemic vasculitis [PDF]

Frontiers in Immunology, 2015
Systemic vas culitis is a heterogeneous group of disorders characterized by inflammation and necrosis in the vessel wall. the diagnosis of a systemic vasculitis is challenging, because patients usually present a broad spectrum of manifestations that vary
Alexandre Wagner Silva De Souza
doaj +7 more sources

Plasmapheresis for systemic vasculitis. [PDF]

Ther Apher Dial, 2022
AbstractSystemic vasculitides include a variety of, and numerous diseases. In 2012, the International CHAPEL HILL Consensus Conference (CHCC2012) led to a major reorganization of the classification of vasculitis, and this is still in wide use today. Although the results of plasmapheresis for individual diseases have been sometimes shown, there are few ...
Fukuoka K +4 more
europepmc +3 more sources

Neurological Involvement in Primary Systemic Vasculitis

Frontiers in Neurology, 2019
Primary systemic vasculitis can affect every structure in both the central and peripheral nervous system, causing varied neurological manifestations of neurological dysfunction.
Shanshan Zhang, Dong-li Yuan, G. Tan
exaly +2 more sources

Immunogenicity and safety to SARS-Cov-2 vaccination in patients with systemic vasculitis [PDF]

Frontiers in Immunology
Background/objectivesPatients with systemic vasculitis faced the risk of severe COVID-19 and high mortality during the pandemic. Although SARS-CoV-2 vaccination mitigates these outcomes, vaccine hesitancy persists, and data on immunogenicity and safety ...
Erika Biegelmeyer +48 more
doaj +2 more sources

Pregnancy and Systemic Vasculitis

Indian Journal of Rheumatology, 2016
The systemic vasculitides are rare diseases of vessel wall inflammation. They are classified according to the vessel wall size. Systemic vasculitis is usually diagnosed after the fifth decade of life, except Takayasu arteritis and Bechet's disease which can manifest earlier.
Himanshu Pathak, Chetan Mukhtyar
doaj +4 more sources

Systemic vasculitis: one year in review 2023.

Clinical and Experimental Rheumatology, 2023
Systemic vasculitides are heterogeneous disabling diseases characterised by chronic inflammation of the blood vessels potentially leading to tissue destruction and organ failure.
M. Moretti +12 more
semanticscholar +1 more source

Cardiovascular events and the role of accelerated atherosclerosis in systemic vasculitis.

Atherosclerosis, 2021
The spectrum of inflammatory blood vessel diseases includes both atherosclerosis and the primary systemic vasculitides. Although the inciting triggers differ, significant overlap exists in the mechanisms that contribute to sustained inflammation and ...
Alison H. Clifford, J. C. Cohen Tervaert
semanticscholar +1 more source

Outcomes of COVID-19 in patients with primary systemic vasculitis or polymyalgia rheumatica from the COVID-19 Global Rheumatology Alliance physician registry: a retrospective cohort study

The Lancet Rheumatology, 2021
Background Patients with primary systemic vasculitis or polymyalgia rheumatica might be at a high risk for poor COVID-19 outcomes due to the treatments used, the potential organ damage cause by primary systemic vasculitis, and the demographic factors ...
S. Sattui +311 more
semanticscholar +1 more source

The modern therapy of systemic vasculitides: perspectives and challenges [PDF]

Терапевтический архив, 2018
Systemic vasculitis is a heterogeneous group of inflammatory diseases, which are classified according to the diameter of the affected vessels. The treatment of systemic vasculitis is no longer empirical, because of increasing number of randomized ...
P.I. NOVIKOV, A.S. ZYKOVA, S.V. MOISEEV
doaj +2 more sources

Human hepatitis viruses-associated cutaneous and systemic vasculitis

World Journal of Gastroenterology, 2021
Human hepatitis viruses (HHVs) include hepatitis A virus, hepatitis B virus (HBV), hepatitis C virus (HCV), hepatitis delta virus, and hepatitis E virus and can cause liver inflammation in their common human host.
Chrong-Reen Wang, H. Tsai
semanticscholar +1 more source

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granulomatosis with polyangiitis
autoantibodies
polyarteritis nodosa