Results 41 to 50 of about 1,041,956 (191)

Nonspecific interstitial pneumonia and cutaneous vasculitis as initial manifestations of Sjögren’s disease: a case report [PDF]

open access: yesRomanian Journal of Rheumatology
Background. Sjögren’s disease is a systemic autoimmune disorder classically characterized by sicca symptoms due to exocrine gland involvement. However, extraglandular manifestations may precede glandular symptoms and pose significant diagnostic ...
Ashaq Hussain Parrey   +2 more
doaj   +1 more source

Clinical and immunological features of retinal vasculitis in systemic diseases [PDF]

open access: yesVojnosanitetski Pregled, 2009
Background/Aim. Vasculitis is a clinical, pathologic process characterized by inflammation and necrosis of blood vessel occurring anywhere in the body.
Paović Jelena   +2 more
doaj   +1 more source

Cardiac Involvement in Systemic Vasculitis

open access: yes, 2017
Systemic vasculitides are a heterogeneous group of diseases characterized by inflammation of vessels, which can result in their obstruction and/or aneurysm formation.
FERRI, Clodoveo   +5 more
core   +1 more source

One year in review 2017: systemic vasculitis

open access: yes, 2017
Systemic vasculitis is a group of heterogeneous, disabling disorders. Great interest has recently arisen in pathophysiology, clinical phenotypes and therapy of large- and small-vessel vasculitis.
Lepri, Gemma   +6 more
core   +2 more sources

Thrombotic microangiopathy in patients with systemic vasculitis: A systematic literature review

open access: yesUlusal Romatoloji Dergisi
Features of thrombotic microangiopathy (TMA) rarely arise in patients with systemic vasculitis. We identified cases in which patients with systemic vasculitis developed clinical, laboratory, and/or histopathological features of TMA.
Ege Sinan Torun, Selin Çelen
doaj   +1 more source

Pregnancy in Systemic Vasculitis

open access: yes, 2020
Conception, pregnancy and childbirth are a biological necessity, a unique privilege and birthright and yet something that mothers suffering with vasculitis cannot take for granted.
Mukhtyar, Chetan   +3 more
core   +1 more source

Recurrent cutaneous eosinophilic vasculitis: A rare entity

open access: yesIndian Journal of Dermatology, 2016
Recurrent cutaneous necrotizing eosinophilic vasculitis is a rare entity described by Chen et al. It has a benign course without any systemic involvement. However, often long-term treatment with systemic steroids is required.
Najeeba Riyaz   +5 more
doaj   +1 more source

Retrospective analysis of scleritis or peripheral ulcerative keratitis in systemic vasculitis: insights from a single tertiary centre

open access: yesClinical Medicine
Introduction: Ocular manifestations of systemic vasculitis are rare and often difficult to treat, resulting in increased morbidity for affected patients.
Lucy Hong   +5 more
doaj   +1 more source

De novo isolated gastrointestinal tract vasculitis without associated systemic disease in renal transplant recipients successfully treated with rituximab

open access: yesSaudi Journal of Kidney Diseases and Transplantation, 2020
Systemic vasculitic diseases can show recurrence after kidney transplantation, but de novo systemic vasculitis is rarely seen after kidney transplantation, and in literature, there are only a few cases.
Cigdem Mengus   +5 more
doaj   +1 more source

Systemic vasculitis: one year in review 2022

open access: yes, 2022
Systemic vasculitis are rare heterogeneous disorders potentially involving any organ and system with a relevant burden of mortality and comorbidity. As in the previous annual reviews of this series, in this review we will provide a critical digest of the
Treppo, Elena   +12 more
core   +2 more sources

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