Posterior Flashcards

1
Q

Acute multifocal retinitis

A

self-limited, preceded by a flu-like. may be an atypical presentation of cat-scratch. sudden onset mild visual loss in young adults

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2
Q

Secondary Frosted branch angiitis

A

associated with infectious retinitis, notably cytomegalovirus retinitis, toxoplasmosis and other conditions such as lymphoma, leukaemia, Behcet, SLE

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3
Q

(Unilateral) acute idiopathic maculopathy (AIM)

A

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

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4
Q

Krill disease

A

Acute retinal pigment epitheliitis

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5
Q

Acute retinal pigment epitheliitis

A

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

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6
Q

Progressive subretinal fibrosis and uveitis syndrome (SFU)

A

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.

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7
Q

Acute idiopathic blind spot enlargement syndrome (AIBSE)

A

many features with MEWDS. young to middle-aged women. Features include photopsia and decreased vision, with blind spot enlargement and mild disc swelling

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8
Q

Acute macular neuroretinopathy (AMN)

A

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.

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9
Q

Acute macular neuroretinopathy (AMN) - FA

A

normal or shows faint hypofluorescence.

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10
Q

Acute syphilitic posterior placoid chorioretinopathy

A

characterized by large pale-yellowish subretinal lesions in the posterior pole

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11
Q

‘ground glass’ appearance

A

syphilitic retinitis

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12
Q

syphilitic retinitis

A

Retinitis has a ‘ground glass’ appearance; associated vasculitis may be occlusive and involve both arteries and veins

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13
Q

Presumed ocular histoplasmosis syndrome

A

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.

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14
Q

Acute retinal necrosis

A

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

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15
Q

Progressive retinal necrosis

A

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.

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16
Q

‘cracked mud’

A

Progressive retinal necrosis

17
Q

Cytomegalovirus retinitis

A

One eye is usually affected initially, progressing to both eyes in 50%. one or two areas of dense white retinal infiltration associated prominently with flame-shaped retinal haemorrhages (‘pizza pie’ or ‘Margherita pizza’), beginning peripherally (centrally in 10%) and extending along the course of the vascular arcades

18
Q

Immune recovery uveitis

A

This is a cause of limited visual outcome in CMV retinitis, thought to be due to a rejuvenated immune response against residual viral antigen following immune reconstitution with HAART. Manifestations can be severe, progressing to phthisis in some cases.

19
Q

Diffuse unilateral subacute neuroretinitis

A

presence of a single motile subretinal nematode such as Toxocara canis, Baylisascaris procyonis and Ancylostoma caninum

20
Q

Diffuse unilateral subacute neuroretinitis - treatment

A

Photocoagulation (200 μm, 0.2–0.5 s, 150–300 mW) is the treatment of choice when a worm can be visualized. Systemic albendazole (400 mg for 30 days) or vitrectomy.

21
Q

Most frequent retinopathy in patients with AIDS

A

HIV-related retinal microangiopathy, developing in up to 70% of patients

22
Q

Congenital toxoplasmosis - treatment

A

pyrimethamine, sulfadiazine, folinic acid