Posterior Flashcards
Acute multifocal retinitis
self-limited, preceded by a flu-like. may be an atypical presentation of cat-scratch. sudden onset mild visual loss in young adults
Secondary Frosted branch angiitis
associated with infectious retinitis, notably cytomegalovirus retinitis, toxoplasmosis and other conditions such as lymphoma, leukaemia, Behcet, SLE
(Unilateral) acute idiopathic maculopathy (AIM)
self-limited unilateral, may be preceded by a flu-like. sudden marked reduction in central vision. An irregularly yellow or grey exudative retinal detachment at macula
Krill disease
Acute retinal pigment epitheliitis
Acute retinal pigment epitheliitis
self-limited condition of the RPE; it is unilateral in 75%, young adults with mild disturbance of central vision; 1–2 weeks after the onset of symptoms the macula shows 2–4 discrete clusters of subtle small (one-fourth disc diameter) grey spots at the level of the RPE, surrounded by hypopigmented yellow haloes
Progressive subretinal fibrosis and uveitis syndrome (SFU)
causing gradual blurring of vision in one then both eyes. Anterior uveitis and vitritis accompanies subretinal mounds (kopce) at the posterior pole and midperiphery. to widespread subretinal fibrosis. Steroids may be effective early in the disease, but the prognosis is poor.
Acute idiopathic blind spot enlargement syndrome (AIBSE)
many features with MEWDS. young to middle-aged women. Features include photopsia and decreased vision, with blind spot enlargement and mild disc swelling
Acute macular neuroretinopathy (AMN)
self-limited, healthy young adult females. one or both eyes and may be preceded by a flu-like illness. Symptoms consist of decreased vision and paracentral scotomata. Red–brown wedgeshaped lesions are observed in a flower petal arrangement around the centre of the macula. FA is normal or shows faint hypofluorescence.
Acute macular neuroretinopathy (AMN) - FA
normal or shows faint hypofluorescence.
Acute syphilitic posterior placoid chorioretinopathy
characterized by large pale-yellowish subretinal lesions in the posterior pole
‘ground glass’ appearance
syphilitic retinitis
syphilitic retinitis
Retinitis has a ‘ground glass’ appearance; associated vasculitis may be occlusive and involve both arteries and veins
Presumed ocular histoplasmosis syndrome
Histoplasma capsulatum, common in AIDS, immunemediated response to microbial antigen. asymptomatic unless macular choroidal neovascularization supervenes. • Classic triad: (i) multiple white atrophic chorioretinal ‘histo’ spots about 200 μm in diameter; (ii) peripapillary atrophy; (iii) vitritis is absent. HLA-B7 and DRw2.
Acute retinal necrosis
healthy, young HSV, old VZV, uni, floaters, pain. 1. Prominent anterior uveitis and vitritis (panuveitis). Episcleritis and scleritis may occur. 2. One or more discrete foci of peripheral retinal necrosis. 3. Circumferential spread of retinal involvement 4. Occlusive retinal vasculitis including arteritis 5. Rapid without treatment
Progressive retinal necrosis
rapidly progressive unilateral or bilateral visual loss, Anterior uveitis and vitritis are minimal. ○ Early. Multifocal homogeneous yellow–white deep retinal infiltrates. The macula may be involved at an early stage, often giving a cherry-red spot.
○ Established/middle. The signs typically spread rapidly around the retina, with very extensive full-thickness necrosis
○ Late. Scarring is plaque-like and characterized as ‘cracked mud’. Rhegmatogenous retinal detachment (RRD) is very common, as is optic atrophy.