Retina and Retinal Pigment Epithelium Flashcards

1
Q

What does the image describe?

A

The normal retinal layers.

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2
Q

What part of the eye is identified in these images?

A

The normal macula.

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3
Q

What is this condition? And what do the photomicrographs illustrate?

A

Albinism.

The nuclei and decreased pigmentation in the RPE and rare giant melanosomes.

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4
Q

What conditions are described in these images? And what is noted in the H&E stain?

A

Leukocoria and total exudative retinal detachment. And dense subretinal proteinaceous fluid.

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5
Q

What do the markings indicate in these images?

A

Telangiectatic vessels and foamy macrophages, and lipid-laden and pigment-laden macrophages and cholesterol clefts.

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6
Q

What is demonstrated in the low-magnification photomicrograph? And what does the higher magnification (PAS stain) shows?

A

A retinal tumor with a thick-walled feeder vessel and a cystic area filled with proteinaceous material. And numerous small, capillary-like vascular channels and foamy stromal cells.

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7
Q

What is the characteristic of the RPE cells?

A

Larger and contain more densely packed melanin granules.

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8
Q

What condition is describe? And what do the arrows indicate?

A

Acute retinal necrosis (ARN) and full-thickness necrosis of the retina.

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9
Q

What condition is this? And what is demonstrated in each image?

A

Cytomegalovirus (CMV) retinitis.

Vascular sheathing, full-thickness retinal necrosis, large syncytial cells, intranuclear owls eye inclusions and intracytoplasmic inclusions.

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10
Q

What is this condition? And what is demonstrated in the stains?

A

Fungal chorioretinitis. And multinucleated giant cells and numerous fungal hyphae.

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11
Q

What do the arrows indicate?

A

Chorioretinal scars with pigmentation, active retinitis and perivascular sheathing, and cysts and released organisms.

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12
Q

What does the image describe?

A

Cystoid spaces in the outer plexiform layer and reticular peripheral cystoid degeneration.

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13
Q

What condition is this?

A

Retinal lattice degeneration.

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14
Q

What do the arrows demonstrate? And what do the arrowheads indicate?

A

Paving-stone degeneration in the areas of depigmentation. And a sharp boundary.

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15
Q

What is the condition described? And what do INL and ONL means?

A

Inner ischemic retinal atrophy. Inner nuclear layer and outer nuclear layer.

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16
Q

What condition is described in this image? And what do the arrow and arrowhead demonstrate?

A

Outer ischemic retinal atrophy.

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17
Q

What is described in this image? And what type of fluid is in the cystoid spaces?

A

Cytoid bodies within the NFL and proteinaceous fluid.

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18
Q

What is this macular disorder? And what is found in the inner nuclear and outer plexiform layers?

A

Cystoid macular edema and cystoid spaces.

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19
Q

What type of deposit is this?

A

Intraretinal lipid deposits, or hard exudates.

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20
Q

What are the features showed in the PAS stain?

A

Intraretinal exudates surround intraretinal microvascular abnormalities.

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21
Q

What is the characteristic of the macula in the first image?

A

Presence of mild cystoid macular edema, subretinal fluid, and irregular elevation and detachment of the RPE.

22
Q

What are the characteristics of the hemorrhages in the fundus photograph? And what are their corresponding places histologically?

A

The dot-blot hemorrhage corresponding to blood in the middle layers of the retina, flame-shaped corresponds to blood in the NFL, and the boat-shaped corresponds to subhyaloid blood.

23
Q

What is described in this trypsin digest?

A

The acellular capillaries are adjacent to intraretinal microvascular abnormalities (IRMA).

24
Q

What is the technique used? And what does it shows?

A

Retinal trypsin digest preparation and diabetic microaneurysms.

25
Q

What does the PAS stain describe?

A

Retinal neovascularization.

26
Q

What is this condition? And what is the characteristic of the retina?

A

Central retinal artery occlusion (CRAO) and necrosis occur in the inner retina and pyknotic nuclei.

27
Q

What is this condition? And what are the characteristics described?

A

Central retinal vein occlusion (CRVO) and hemorrhage, hemosiderosis, disorganization of the retinal architecture, and gliosis.

28
Q

What does the photomicrograph demonstrate? And what condition has these histologic changes?

A

Iris neovascularization, lacy vacuolation, and thickening of the basement membrane of the pigmented ciliary epithelium. And diabetes mellitus.

29
Q

What occurs after light applications of laser photocoagulation?

A

Focal disruption and attenuation of the outer nuclear layer, inner/outer segments, and RPE.

30
Q

What is described in this image?

A

Choroidal neovascularization between the diffuse drusen and Bruch membrane.

31
Q

What type of drusen is this?

A

Hard drusen.

32
Q

What type of drusen is this? And what is the characteristic?

A

Confluent drusen and thick eosinophilic deposits.

33
Q

What type of drusen is this?

A

Reticular pseudodrusen.

34
Q

What does the fundus photograph demonstrate? And what are the histologic characteristics?

A

Focal geographic atrophy of the RPE and drusen in nonexudative age-related macular degeneration.

35
Q

What type of neovascularization are these? And where are they located?

A

Type 1 neovascularization, located in the sub-RPE space, and type 2 neovascularization occurs in the subretinal space.

36
Q

What disorder is this? And what are the characteristics?

A

Polypoidal choroidal vasculopathy (PCV). Peripapillary dilated vascular channels, thin-walled vascular channels, and hemorrhagic RPE detachments.

37
Q

What are the characteristics of the lesions in these images?

A

Elevated, red-orange, nodular and tubular lesions, hyperfluorescent polypoidal lesions, and persistent red-orange lesions in the peripapillary region.

38
Q

What does the fundus photograph show? And what do the asterisks in the FAF imaging reveals?

A

Retinal flecks and focal or geographic RPE atrophy. And increased and decreased FAF.

39
Q

What are the highlights in near-infrared imaging? And what does the histology report reveals?

A

The increased reflectance and hyperreflectivity at the level of RPE. And lipofuscin corresponding to the retinal flecks and loss of the photoreceptor cell layer.

40
Q

What is this condition? And what is the highlight in the images?

A

Adult-onset foveomacular vitelliform dystrophy. And increased FAF, subfoveal hyperreflective material, and pigment-containing cells filled with lipofuscin.

41
Q

What is this condition? And what are the histologic characteristics noted?

A

Retinitis pigmentosa and marked photoreceptor cell loss and RPE migration.

42
Q

What is this condition? And what is the histologic arrangement?

A

Retinoblastoma and pseudorosette.

43
Q

What is present in the necrotic area? And what is found within the blood vessel walls?

A

Calcium and basophilic material.

44
Q

What are the features noted in this image? And what is the characteristic of the tumor cells?

A

Thick iris neovascular membrane and free-floating tumor cells.

45
Q

What type of rosettes are these? And what is the characteristic?

A

Flexner-Winstersteiner rosettes and Homer Wright rosettes. And central lumen and the neurofibrillary tangle.

46
Q

What does the arrow indicate?

A

The fleurette.

47
Q

What is the characteristic of the globe in image A? And what is present in the nerve?

A

Massive invasion by retinoblastoma with bulbous enlargement of the optic nerve and tumor.

48
Q

What is the extent of the retinoblastoma?

A

Optic nerve and extended posterior to the lamina cribrosa to the margin of resection.

49
Q

What is the histologic feature described in this image?

A

Massive choroidal invasion of the retinoblastoma.

50
Q

What is this condition? And what is the characteristic?

A

Retinocytoma and stubby inner segments.

51
Q

What condition is this? And what are the histologic features?

A

Medulloepithelioma and ciliary process and occasional Flexner- Winstersteiner rosettes.

52
Q

What type of lesions are these? And what is the characteristic?

A

Combined hamartoma of the retina and RPE. And the presence of a slightly elevated, variably pigmented mass involving the RPE, peripapillary retina, optic nerve, and overlying vitreous.