Lab 3 - Peripheral Retina Flashcards

1
Q

What is the difference between retinoschisis and retinal detachment?

A

Retinoschisis is usually bilateral whilst retinal detachment is generally unilateral.

Retinoschisis is immobile whilst retinal detachment may be mobile.

Retinoschisis results in an absolute visual field defect whereas retinal detachment results in a relative visual field defect

Retinoschisis tends to affect hyperopes whereas retinal detachment tends to affect myopes

Retinoschisis results in outer-inner retinal breaks whereas retinal detachment is a full thickness retinal break.

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2
Q

Describe what you would see upon fundoscopy of a patient with posterior vitreous detachment

A

Diffuse blurriness of image

Weiss ring - if detached from ONH

Shafer’s sign - brown pigment in vitreous that suggests a retinal tear has occured

Vitreous haemorrhage

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3
Q

What are the two kinds of retinal breaks?

A

Tear - horse-shoe shaped

Hole - atrophic / operculated

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4
Q

List the 3 kinds of retinal detachments, how they occur and what you would find upon fundoscopy

A

Rhegmatogenous

  • retinal break present
  • shafer’s sign may be present

Serous/Exudative

  • no retinal break
  • fluid accumulation below superficial retina
  • dome shaped retina - looks as if a section of retina blurred or dark

Tractional

  • secondary to previous haemorrhage, surgery, trauma, infarct, inflammation etc
  • fibrotic/fibrovascular membranes = traction on retina
  • immobile/does not shift with head movements
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5
Q

What is the difference between lattice and pavingstone degeneration?

A

Lattice
- linear trail of fibrosed vessels within atrophied retina in a lattice pattern
- atrophic holes often present
predispose to RRD

Pavingstone

  • degeneration of choriocapillaris = reduced RPE
  • areas of yellow thinned retina with increased visibility of choroidal vasculature with hyperpigmented margins
  • does NOT predispose to retinal detachment
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6
Q

Describe what you would see upon fundoscopy of a patient with retinoschisis

A

Balooning retinal elevation with clearly demarcated borders

Holes may develop in inner/outer layers

Similar to RRD but immobile, asymptomatic and causes an absolute scotoma.

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7
Q

Describe what you would see upon fundoscopy of a patient with WWOP

A

grey/white, somewhat translucent retina

- looks like a foggy/desaturated retina with a clearly demarcated area

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8
Q

What is the pathophysiology of PVD

A

Aging results in a reduction of hyaluronic acid, resulting in a loss of support to collagen.

Fine collagen fibrils congregate, forming small floating opacities.

The vitreous moves more readily with eye movement and trauma, tugging the hyaloid membrane away from the inner limiting membrane.

The vitreous may collapse, with detachment of posterior hyaloid face from the ONH

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9
Q

What is the pathophysiology of lattice degeneration?

A

Dropout of peripheral retinal capillaries results in ischaemia, leading to thinning of all retinal layers. This causes:

Disturbance of the overlying vitreous which casues pockets of liquefaction overlying lattice lesions

Strong vitreoretinal adhesion along edges of lattice lesion

Disturbs RPE = RPE hyperplasia and pigmented appearance

Sclerosis of larger vessels gives lattice its characteristic fibrotic appearance

Retinal thinning can become so profound that a full thickness hole atrophies through retina at lattice lesion, leading to RRD

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10
Q

What is the pathophysiology of pavingstone degeneration?

A

Degeneration of choriocapillaris leads to subsequent loss of RPE
- allows direct contact between remaining thinned neural retina and choroidal connective tissue

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11
Q

What is the pathophysiology of retinoschisis

A

Splitting within retina at outer plexiform layer.

Degenerative form, due to coalescence of cysts from microcystoid degeneration. Retina splits into inner and outer cavity if enough cystic spaces coalesce

Inner/outer/both layers may develop holes, leading to RRD (if in outer layer)

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