نتایج جستجو برای: idiopathic retinal vasculitis

تعداد نتایج: 155576  

2010
Marcelo Derbli Schafranski Giuliano Doretto Campanari

Cutaneous vasculitis can be classified as primary or idiopathic; or secondary, when it presents as a manifestation of connective tissue diseases, infections, drug reactions or malignancies. Although most of the idiopathic cases are self-limited and responsive to supportive measures and nonsteroidal anti-inflammatory drugs, potent immunosuppressants are sometimes required for the management of t...

Journal: :Clinical and experimental rheumatology 2004
J O Susac L H Calabrese E Baylin R A Prayson N E Medeiros R P Hull J P Tucker

A 39-year-old woman presented with multiple branch retinal artery occlusions almost three years before developing a mass lesion containing calcium in the left frontal lobe. Brain biopsy revealed a small vessel vasculitis and ischemic necrosis of brain with dystrophic calcification. We believe this to be the first case of primary CNS vasculitis with branch retinal artery occlusions and brain cal...

2018
Manisha Agarwal Ankita Shrivastav Abdul Waris

BACKGROUND Tubercular vasculitis is an important manifestation of ocular tuberculosis and this report highlights the mimicking nature of the disease with frosted branch angiitis. RESULTS A patient presented with a severe form of retinal vasculitis in both eyes and a branch retinal vein occlusion in the left eye. He had a positive tuberculin skin test (TST) and a raised erythrocyte sedimentati...

Journal: :Postgraduate medical journal 1995
M Garcia-Diaz M Mira L Nevado A Galván A Berenguer J C Bureo

Although systemic vasculitis can be a complication of inflammatory bowel disease at several locations (skin, eyes, brain, mesentery, and lung) the association of retinal vasculitis with Crohn's disease is rare. We studied a 26-year-old woman with biopsy-demonstrated Crohn's disease who developed a severe bilateral retinal arteritis and phlebitis, with acute loss of vision.

Journal: :medical hypothesis, discovery and innovation ophthalmology journal 0
a. osman saatci ziya ayhan fatos onen zeynep ozbek ismet durak

we report a 32-year-old man with behçet’s disease who had simultaneous bilateral anterior uveitis, unilateral nodular scleritis and occlusive vasculitis with retinal hemorrhages at the same time. though scleritis is not considered within  the classical features of behçet’s disease behçet’s disease should be contemplated in the scleritis etiology.

Journal: :iranian journal of medical sciences 0
f. davatchi rheumatology research center, shariati hospital, tehran university for medical sciences, tehran, iran. h. shams rheumatology research center, shariati hospital, tehran university for medical sciences, tehran, iran. f. shahram rheumatology research center, shariati hospital, tehran university for medical sciences, tehran, iran. a. nadji rheumatology research center, shariati hospital, tehran university for medical sciences, tehran, iran. a.r. jamshidi rheumatology research center, shariati hospital, tehran university for medical sciences, tehran, iran. c. chams-davatchi rheumatology research center, shariati hospital, tehran university for medical sciences, tehran, iran.

background: the natural history of ocular lesions in behçet's disease is toward severe loss of vision/blindness in few years, whereas cytotoxic drugs have changed the outcome. several open labeled cohort studies showed pulse cyclophosphamide (pcp) to be the best choice. since one third of these patients are resistant to pcp it is important to know how much improvement one can expect from the re...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید