OCULAR DISEASE DEFINITION TERMS Flashcards

(50 cards)

1
Q

Blockage of the main vein of the retina, leading to retinal hemorrhages, edema, and vision loss.

A

CENTRAL RETINAL VEIN OCCLUSION

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2
Q

Blockage of the main artery of the retina, causing sudden vision loss, often described as a curtain or shade coming down.

A

CRAO

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3
Q

Blockage of a smaller retinal vein, leading to localized retinal hemorrhages and edema.

A

BRVO

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4
Q

Early stage of diabetic retinopathy, characterized by microaneurysms, dot hemorrhages, and hard exudates.

A

Background Diabetic Retinopathy

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5
Q

Advanced stage of diabetic retinopathy, marked by growth of new, fragile blood vessels (neovascularization), which can lead to vitreous hemorrhage and retinal detachment.

A

PDR
PROLIFERATIVE DR

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6
Q

Intermediate stage of diabetic retinopathy, characterized by more extensive retinal damage, including hemorrhages, hard exudates, and cotton wool spots.

A

NPDR

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7
Q

progressive condition where the drainage channels in the trabecular meshwork become less efficient, leading to increased intraocular pressure and optic nerve damage.

A

POAG

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8
Q

condition where the iris blocks the drainage angle, causing a sudden increase in intraocular pressure, often accompanied by severe eye pain, headache, and vision loss.

A

PACG

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9
Q

condition where fluid accumulates under the retina, causing a detachment and leading to blurred vision, often affecting young to middle-aged adults (men) who takes corticosteroids and under stress

A

CSR CENTRAL SEROUS RETINOPATHY

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10
Q

viral infection of the retina, often seen in immunocompromised individuals, such as those with HIV/AIDS, leading to retinal inflammation, hemorrhages, and necrosis.

A

CMVR (Cytomegalovirus Retinitis)

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11
Q

Progressive thinning and conical protrusion of the cornea, leading to distorted vision. Hallmarks include corneal thinning, conical shape, and irregular astigmatism.

A

Keratoconus

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12
Q

genetic disorder causing corneal endothelial dysfunction, leading to corneal edema and vision loss. Hallmarks include corneal guttae, edema, and decreased endothelial cell density.

A

Fuchs’ Dystrophy

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13
Q

Inflammation of the uveal tract, causing pain, redness, and vision loss. Hallmarks include inflammation in the anterior or posterior segment, cells and flare in the anterior chamber.

A

Uveitis

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14
Q

type of cancer originating from melanocytes in the uvea, often asymptomatic in early stages. Hallmarks include a pigmented mass in the choroid or iris, and characteristic ultrasound or MRI findings.

A

MELANOMA

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15
Q

genetic disorder causing progressive degeneration of the retina, leading to night blindness and visual field loss. Hallmarks include bone spicule pigmentation, attenuated retinal vessels, and electroretinogram (ERG) abnormalities.

A

Retinitis Pigmentosa

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16
Q

condition where the vitreous gel adheres too strongly to the macula, causing distortion and vision loss. Hallmarks include vitreomacular adhesion and tractional forces on the retina.

A

Vitreomacular Traction Syndrome

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17
Q

type of glaucoma where optic nerve damage occurs despite normal intraocular pressure. Hallmarks include optic disc cupping, visual field defects, and normal IOP.

A

Normal-Tension Glaucoma

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18
Q

Inflammation of the eyelids, causing redness, itching, and crusting. Hallmarks include eyelid inflammation, crusting, and meibomian gland dysfunction.

A

Blepharitis

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19
Q

Inflammation of the conjunctiva, causing redness, itching, and discharge. Hallmarks include conjunctival injection, discharge, and chemosis.

A

Conjunctivitis

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20
Q

Drooping of the eyelid, which can be congenital or acquired. Hallmarks include drooping eyelid, decreased palpebral fissure height, and potential amblyopia in children.

A

PTOSIS

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21
Q

Involuntary eye movements, which can be congenital or acquired. Hallmarks include repetitive, rhythmic eye movements, and potential visual impairment.

22
Q

Progressive degeneration of the macula, leading to central vision loss. Hallmarks include drusen, geographic atrophy, and choroidal neovascularization.

A

Age-related Macular Degeneration (AMD)

23
Q

Fluid accumulation under the retina, causing a detachment and blurred vision. Hallmarks include serous retinal detachment and leakage on fluorescein angiography.

A

Central Serous Retinopathy (CSR)

24
Q

Fluid accumulation in the macula, leading to swelling and vision distortion. Hallmarks include retinal thickening and cystoid spaces.

A

Macular Edema

25
full-thickness defect in the macula, causing central vision loss. Hallmarks include a round or oval defect in the fovea.
MACULAR HOLE
26
fibrocellular membrane on the retinal surface, causing vision distortion and blurriness. Hallmarks include a membrane on the retinal surface and retinal distortion.
Epiretinal Membrane (ERM)
27
genetic disorder causing progressive macular degeneration in young people. Hallmarks include flecks in the retina and macular atrophy.
Stargardt Disease
28
Inflammation of the optic nerve, causing vision loss, pain, and color vision disturbances. Hallmarks include decreased visual acuity, impaired color vision, and relative afferent pupillary defect (RAPD).
Optic Neuritis
29
Damage to the optic nerve, leading to vision loss and optic disc changes. Hallmarks include optic disc pallor, cupping, or atrophy.
OPTIC NEUROPATHY
30
Damage to the optic nerve due to increased intraocular pressure, leading to progressive vision loss. Hallmarks include optic disc cupping, thinning of the neuroretinal rim, and visual field defects.
Glaucomatous Optic Neuropathy
31
Damage to the optic nerve due to reduced blood flow, causing sudden vision loss. Hallmarks include optic disc swelling, followed by optic atrophy.
Ischemic Optic Neuropathy
32
genetic disorder causing progressive optic nerve damage and vision loss, often affecting young men. Hallmarks include bilateral optic atrophy and specific mitochondrial DNA mutations.
Leber's Hereditary Optic Neuropathy (LHON)
33
Calcified deposits in the optic disc, which can cause visual field defects. Hallmarks include visible drusen on the optic disc and autofluorescence on imaging.
Optic Disc Drusen
34
A type of cancer originating from melanocytes in the choroid, often asymptomatic in early stages. Hallmarks include a pigmented mass in the choroid, characteristic ultrasound or MRI findings, and potential vision loss.
CHOROIDAL MELANOMA `
35
Growth of new, fragile blood vessels in the choroid, often associated with age-related macular degeneration (AMD). Hallmarks include leakage on fluorescein angiography, retinal edema, and potential vision loss.
Choroidal Neovascularization (CNV)
36
Inflammation of the choroid, often caused by infections or autoimmune disorders. Hallmarks include inflammation in the choroid, potential retinal detachment, and vision loss.
CHOROIDITIS
37
Inflammation of the uveal tract (iris, ciliary body, and choroid), causing pain, redness, and vision loss. Hallmarks include inflammation in the anterior or posterior segment, cells and flare in the anterior chamber, and potential complications like cataracts or glaucoma.
UVEITIS
38
type of cancer originating from melanocytes in the uvea, often affecting the choroid or iris. Hallmarks include a pigmented mass in the uvea, characteristic ultrasound or MRI findings, and potential vision loss.
UVEAL MELANOMA
39
rare, autoimmune condition where inflammation in one eye can trigger inflammation in the other eye, often following trauma or surgery. Hallmarks include bilateral granulomatous uveitis, potential vision loss, and a history of trauma or surgery.
SYMPATHETIC OPHTHALMIA
40
rare, autoimmune condition affecting the uvea, meninges, and skin, causing uveitis, skin depigmentation, and potential vision loss. Hallmarks include bilateral uveitis, skin depigmentation, and meningeal symptoms.
Vogt-Koyanagi-Harada (VKH) Disease
41
genetic disorder causing corneal lattice-like deposits, leading to vision loss. Hallmarks include lattice-like corneal deposits and corneal thinning.
Lattice Corneal Dystrophy
42
genetic disorder causing corneal epithelial irregularities, leading to recurrent erosions and vision problems. Hallmarks include map-like, dot-like, or fingerprint-like corneal patterns.
Map-Dot-Fingerprint Dystrophy
43
Separation of the retina from the underlying tissue, causing vision loss. Hallmarks include retinal detachment, retinal tears, and potential vision loss.
RETINAL DETACHMENT
44
Splitting of the retina's layers, causing vision loss. Hallmarks include retinal splitting, retinal thinning, and potential vision loss.
Retinoschisis
45
rare type of cancer originating from melanocytes in the iris. Hallmarks include a pigmented mass in the iris, characteristic ultrasound or MRI findings.
IRIS MELANOMA
46
rare type of cancer originating from melanocytes in the ciliary body. Hallmarks include a pigmented mass in the ciliary body, characteristic ultrasound or MRI findings.
CILIARY BODY MELANOMA
47
rare condition causing painful ophthalmoplegia due to inflammation in the cavernous sinus. Hallmarks include painful eye movements, ophthalmoplegia, and potential cranial nerve palsies.
Tolosa-Hunt Syndrome
48
Rare conditions associated with cancer, causing retinal or optic nerve damage. Hallmarks include retinal degeneration, optic neuritis, and potential vision loss.
Paraneoplastic Syndromes
49
systemic condition causing granulomatous inflammation in various organs, including the eyes. Hallmarks include uveitis, retinal vasculitis, and potential vision loss.
SARCOIDOSIS
50
systemic condition causing vasculitis and inflammation in various organs, including the eyes. Hallmarks include uveitis, retinal vasculitis, and potential vision loss.
Behçet's Disease