Results 291 to 300 of about 1,552,446 (340)

Imaging features of 18F-FDG PET/CT in different types of systemic vasculitis

Clinical Rheumatology, 2022
Zhuo Chen, Yun-yun Zhao, Qian Wang, Yuan Li, He-bei Li, Yunshan Zhou   +5 more
semanticscholar   +1 more source

Autoantibodies in systemic vasculitis

Australian and New Zealand Journal of Medicine, 1991
Abstract We have studied 495 sera that were referred to us from patients suspected on clinical and/or histological grounds to have a small vessel vasculitis. These sera were tested for antibodies against neutrophil cytoplasm antigens (anti‐neutrophil cytoplasm antibodies, ANCA) using assays based on neutrophil acid extract, myeloperoxidase and elastase.
J A, Savige, M, Gallicchio, L, Chang, J D, Parkin   +3 more
openaire   +2 more sources

Central Nervous System Vasculitis

Current Treatment Options in Neurology, 2013
A patient presenting with suspected primary central nervous system (CNS) vasculitis is often difficult to manage. Once the diagnosis is suspected, the clinical course may already be severe and warrant timely aggressive treatment with potentially toxic drugs.
Marc, Gotkine, Adi, Vaknin-Dembinsky
openaire   +2 more sources

Systemic vasculitis in childhood

Current Rheumatology Reports, 2009
Systemic vasculitis is a group of disorders with multiorgan involvement. These disorders have diverse clinical manifestations associated with significant morbidity and mortality. The most common vasculitides in children--Henoch-Schönlein purpura and Kawasaki disease--are self-limiting conditions.
Abraham, Gedalia, Raquel, Cuchacovich
openaire   +2 more sources

Epidemiology of systemic vasculitis

Current Rheumatology Reports, 2005
The systemic vasculitides are heterogeneous conditions of unknown etiology characterized by inflammation and necrosis of different sized blood vessels. Wegener's Granulomatosis, microscopic polyangiitis, and Churg Strauss syndrome are associated with anti-neutrophil cytoplasmic antibodies and affect small and medium blood vessels. They are very rare in
Lane, S. E., Watts, R. A., Scott, D. G. I.   +2 more
openaire   +2 more sources

Systemic vasculitis.

Clinical and experimental rheumatology, 1993
The systemic vasculitides are comparatively rare but important disorders of childhood. Apart from Henoch-Schönlein purpura, which is the commonest example in paediatric practice, Kawasaki disease is most often encountered. Polyarteritis and Wagener's granulomatosis have a lower incidence but are associated with a high morbidity and mortality.
openaire   +1 more source

Epidemiology of systemic vasculitis

Current Opinion in Rheumatology
Purpose of review Ongoing research contributes to our understanding of the epidemiology of vasculitis and its outcomes across the globe. This review aims to summarize important research studies published on this topic in the last 18 months.
Mehmet, Hocaoglu, Brian, Jaros, Anisha B, Dua, Sebastian E, Sattui   +3 more
openaire   +2 more sources

[Systemic vasculitis].

Journal des maladies vasculaires, 2000
Systemic vasculitis is a general term designating a wide range of sometimes overlapping vascular conditions with marked tropism for peripheral constituting a complex nosological structure. Angiologists must be aware of the different telltale clinical signs including purpura, polyarthritis, glomerulonephritis, polyneuritis and unexplained inflammatory ...
B, Planchon, E, Cassagnau, P, Pottier, M, Pistorius   +3 more
openaire   +1 more source

THERAPY OF SYSTEMIC VASCULITIS

Neurologic Clinics, 1997
The systemic vasculitides represent a highly heterogeneous and complex set of disorders primarily mediated via immunologic mechanisms. Standard therapy of these diseases includes the use of glucocorticoids without the use of additional cytotoxic agents.
openaire   +2 more sources

Systemic (allergic?) vasculitis

Journal of Allergy and Clinical Immunology, 1974
H N, Claman, R M, Karr, P F, Kohler, M F, Mass, R M, McIntosh, W M, Sams, P, Small, R E, Stanford, E G, Thorne   +8 more
openaire   +2 more sources