Results 271 to 280 of about 160,652 (313)
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Journal of Allergy and Clinical Immunology, 2009
The primary systemic vasculitides comprise a broad group of diseases identified by their clinical, histopathologic, and therapeutic characteristics. These unique entities have a broad spectrum of organ involvement and severity, which influences the approach to diagnosis and treatment.
Atul, Khasnis, Carol A, Langford
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The primary systemic vasculitides comprise a broad group of diseases identified by their clinical, histopathologic, and therapeutic characteristics. These unique entities have a broad spectrum of organ involvement and severity, which influences the approach to diagnosis and treatment.
Atul, Khasnis, Carol A, Langford
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Rheumatic Disease Clinics of North America, 2017
Vasculitis is more often a disease of women beyond their reproductive years, leaving the challenges of pregnancy management difficult to study. Pregnancy complications, including pregnancy loss and preterm birth, are higher among women with all forms of vasculitis.
Leah, Machen, Megan E B, Clowse
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Vasculitis is more often a disease of women beyond their reproductive years, leaving the challenges of pregnancy management difficult to study. Pregnancy complications, including pregnancy loss and preterm birth, are higher among women with all forms of vasculitis.
Leah, Machen, Megan E B, Clowse
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Current Opinion in Rheumatology, 2008
There are many disorders that may closely resemble the clinical, radiologic and/or pathologic features of the primary vasculitides. In this review, we focus on recently described and under-recognized syndromes that may mimic vasculitis.Hereditary causes of large-artery aneurysms such as Marfan's syndrome have long been recognized; recent years have ...
Eamonn S, Molloy, Carol A, Langford
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There are many disorders that may closely resemble the clinical, radiologic and/or pathologic features of the primary vasculitides. In this review, we focus on recently described and under-recognized syndromes that may mimic vasculitis.Hereditary causes of large-artery aneurysms such as Marfan's syndrome have long been recognized; recent years have ...
Eamonn S, Molloy, Carol A, Langford
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Current Rheumatology Reports, 2012
The primary systemic vasculitides in childhood are quite rare except for Henoch-Schönlein purpura and Kawasaki disease. These are usually self-limited diseases. The etiopathogenesis for most of them is not clearly understood. However, it is usually thought that environmental triggers (mostly infectious) evoke an aggravated inflammatory response in ...
BATU, EZGİ DENİZ, Ozen, SEZA
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The primary systemic vasculitides in childhood are quite rare except for Henoch-Schönlein purpura and Kawasaki disease. These are usually self-limited diseases. The etiopathogenesis for most of them is not clearly understood. However, it is usually thought that environmental triggers (mostly infectious) evoke an aggravated inflammatory response in ...
BATU, EZGİ DENİZ, Ozen, SEZA
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Rheumatic Disease Clinics of North America, 2007
Until recently, the prognosis associated with many forms of systemic vasculitis was quite grim. Advances in this field have allowed us to begin to focus on issues related to quality of life such as fertility, conception, and pregnancy among women with vasculitis.
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Until recently, the prognosis associated with many forms of systemic vasculitis was quite grim. Advances in this field have allowed us to begin to focus on issues related to quality of life such as fertility, conception, and pregnancy among women with vasculitis.
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Current Rheumatology Reports, 2003
Granulomatous vasculitis is a subset of systemic necrotizing vasculitis and has granulomatous inflammation as the main histopathologic feature. Etiopathogenesis remains poorly understood, although recent advances suggest an important role for certain pro-inflammatory cytokines, such as tumor necrosis factor-alpha.
Javier, Marquez +3 more
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Granulomatous vasculitis is a subset of systemic necrotizing vasculitis and has granulomatous inflammation as the main histopathologic feature. Etiopathogenesis remains poorly understood, although recent advances suggest an important role for certain pro-inflammatory cytokines, such as tumor necrosis factor-alpha.
Javier, Marquez +3 more
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Annals of the New York Academy of Sciences, 2011
[18F]Fluorodeoxyglucose positron emission tomography (FDG PET) can be used to visualize large‐vessel inflammation in giant‐cell arteritis, Takayasu arteritis, and other types of aortitis. In patients with symptoms compatible with polymyalgia rheumatica, findings of increased FDG‐uptake in the shoulders, hips, as well as the spinous processes of the ...
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[18F]Fluorodeoxyglucose positron emission tomography (FDG PET) can be used to visualize large‐vessel inflammation in giant‐cell arteritis, Takayasu arteritis, and other types of aortitis. In patients with symptoms compatible with polymyalgia rheumatica, findings of increased FDG‐uptake in the shoulders, hips, as well as the spinous processes of the ...
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Lupus, 1998
Vasculitis can and does occur in childhood. Apart from the relatively common vasculitides (Henoch–Schönlein purpura, Kawasaki disease and in world wide terms Takayasu disease) there are a number of important but comparatively rare disorders affecting children.
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Vasculitis can and does occur in childhood. Apart from the relatively common vasculitides (Henoch–Schönlein purpura, Kawasaki disease and in world wide terms Takayasu disease) there are a number of important but comparatively rare disorders affecting children.
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Immunology and Allergy Clinics of North America
Urticarial vasculitis is a rare autoimmune disorder characterized by persistent edematous papules and plaques on the skin that last longer than 24 hours, often accompanied by systemic symptoms such as joint pain and fever. Unlike common urticaria, this condition involves inflammation of small blood vessels, leading to more severe and long-lasting skin ...
Ruth X, Wang, Sabrina A, Newman
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Urticarial vasculitis is a rare autoimmune disorder characterized by persistent edematous papules and plaques on the skin that last longer than 24 hours, often accompanied by systemic symptoms such as joint pain and fever. Unlike common urticaria, this condition involves inflammation of small blood vessels, leading to more severe and long-lasting skin ...
Ruth X, Wang, Sabrina A, Newman
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