Search results
Results from the WOW.Com Content Network
Retinal vasculitis is inflammation of the vascular branches of the retinal artery, caused either by primary ocular disease processes, or as a specific presentation of any systemic form of vasculitis such as Behçet's disease, sarcoidosis, multiple sclerosis, or any form of systemic necrotizing vasculitis such as temporal arteritis, polyarteritis nodosa, and granulomatosis with polyangiitis, or ...
Retinal vasculopathy with cerebral leukocencephalopathy and systemic manifestations (RVCL or RVCL-S, also previously known as retinal vasculopathy with cerebral leukodystrophy, RVCL; or cerebroretinal vasculopathy, CRV; or hereditary vascular retinopathy, HVR; or hereditary endotheliopathy, retinopathy, nephropathy, and stroke, HERNS) is an inherited condition resulting from a frameshift ...
Purtscher's retinopathy may also be associated with acute pancreatitis, vasculitis, embolization of such materials as fat and amniotic fluid, [8] systemic lupus erythematosus, thrombotic thrombocytopenic purpura, and chronic kidney failure. [3] Purtscher's retinopathy may be caused by extensive fractures of the long bones. [9]
Treatment is based on the cause of the retinopathy and may include laser therapy to the retina. Laser photocoagulation therapy has been the standard treatment for many types of retinopathy. Evidence shows that laser therapy is generally safe and improves visual symptoms in sickle cell and diabetic retinopathy.
Eales disease is a type of obliterative vasculopathy, also known as angiopathia retinae juvenilis, periphlebitis retinae or primary perivasculitis of the retina.It was first described by the British ophthalmologist Henry Eales (1852–1913) in 1880 [1] and is a rare ocular disease characterized by inflammation and possible blockage of retinal blood vessels, abnormal growth of new blood vessels ...
Currently there is no treatment for this condition, but, it is usually self limiting. [1] Systemic administration of corticosteroids may be advised. [2] Even if the disease is resolved, the enlarged blind spot usually does not return to normal. [5]
Birdshot chorioretinopathy, now commonly named birdshot uveitis or HLA-A29 uveitis, [1] is a rare form of bilateral posterior uveitis affecting both eyes.It causes severe, progressive inflammation of both the choroid and retina.
Long-term systemic Immunosuppressive therapy is the main treatment of cancer-associated retinopathy. [5] It can be treated with a combination of chemotherapy and immunosuppression . [ 2 ] Although tumor removal and cancer regression may result in a decrease in circulating autoantibodies, this does not influence CAR progression.