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  2. Retinal vasculitis - Wikipedia

    en.wikipedia.org/wiki/Retinal_vasculitis

    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 ...

  3. Eales disease - Wikipedia

    en.wikipedia.org/wiki/Eales_disease

    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 ...

  4. Acute posterior multifocal placoid pigment epitheliopathy

    en.wikipedia.org/wiki/Acute_posterior_multifocal...

    Rarely, coexisting vasculitis may cause neurological complications. These occurrences can start with mild headaches that steadily worsen in pain and onset, and can include attacks of dysesthesia. This type of deterioration happens usually if the lesions involve the fovea. [2] [15]

  5. Vasculitis - Wikipedia

    en.wikipedia.org/wiki/Vasculitis

    The definite diagnosis of vasculitis is established after a biopsy of involved organ or tissue, such as skin, sinuses, lung, nerve, brain, and kidney. The biopsy elucidates the pattern of blood vessel inflammation. Some types of vasculitis display leukocytoclasis, which is vascular damage caused by nuclear debris from infiltrating neutrophils. [37]

  6. Behçet's disease - Wikipedia

    en.wikipedia.org/wiki/Behçet's_disease

    A rare form of ocular (eye) involvement in this syndrome is retinal vasculitis which presents with painless decrease of vision with the possibility of floaters or visual field defects. [4] Optic nerve involvement in Behçet's disease is rare, typically presenting as progressive optic atrophy and visual loss.

  7. Relapsing polychondritis - Wikipedia

    en.wikipedia.org/wiki/Relapsing_polychondritis

    [3] [4] There are also other ocular manifestations that occur in persons with RP, these include keratoconjunctivitis sicca, peripheral keratitis (rarely with ulcerations), anterior uveitis, retinal vasculitis, proptosis, lid edema, keratoconus, retinopathy, iridocyclitis and ischemic optic neuritis that can lead to blindness.

  8. List of systemic diseases with ocular manifestations - Wikipedia

    en.wikipedia.org/wiki/List_of_systemic_diseases...

    Central retinal artery occlusion; Cardiac myxoma; Cranial arteritis; Sickle cell attack; Occlusive vascular disease (slow, progressive) Carotid artery disease; Arterial spasm (TIA) Diabetes mellitus; Collagen diseases; Venous occlusive disease; Thrombosis; Use of hormonal contraception; Endocarditis; Myxoma; Aortic arch syndrome (takayasu) Pre ...

  9. Birdshot chorioretinopathy - Wikipedia

    en.wikipedia.org/wiki/Birdshot_chorioretinopathy

    Substantial reduction and even stabilization of both vitreous inflammation and retinal vasculitis have been evident via electroretinography, during daclizumab (IL-2 receptor blocker) therapy. This is also supported by the observation of elevated levels of IL-2 in the eyes of patients. [6]