Unit 2 part 1 Flashcards

1
Q

In what layer are the opacities in infectious crystalline keratopathy found?

A

Stroma

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2
Q

In what layer are the opacities in filamentary keratopathy found?

A

Epithelial

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3
Q

What is the most commonly associated pathogen in infectious crystalline keratopathy?

A

Steptococcus viridans

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4
Q

What is the general cause for infectious crystalline keratopathy?

A

Long term steroid use

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5
Q

What causes thygeson superficial punctate keratitis?

A

Idiopathic

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6
Q

How is infectious crystalline keratopathy treated?

A

Topical antibiotics

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7
Q

How is Thygeson superfical punctate keratitis treated?

A

Lubricants and steroids initially followed by bandage CL and PTK

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8
Q

What are the symptoms of Thygeson superficial keratitis?

A

irritation and watering

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9
Q

What are the symptoms of filamentary keratopathy?

A

Photophobia, dicomfort and redness

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10
Q

What is the treatment of filamentary keratopathy?

A

Treat underlying cause, remove filaments, use mucolytics, hypotonic saline, intensive lubrication , bandage cl, NSAI drops

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11
Q

What are the causes of filamentary keratopathy

A

Aqueous deficiency, CL overwear, REES, eye closure

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12
Q

What is the difference between a corneal dystrophy and corneal keratopathies?

A

Dystrophies are bilateral, genetically determined, progressive.

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13
Q

In what layer is Cogan dystrophy found?

A

Epithelial

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14
Q

What else is Cogan’s dystrophy called?

A

Map/dot, fingerprint

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15
Q

At what stage of life is Cogan diagnosed?

A

2/3rd decade

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16
Q

What symptoms are there with Cogan’s dysrophy?

A

Often asymptomatic but if symptomatic then REES without history of trauma

17
Q

What is the histological appearance of Cogan’s?

A

Fibril proten deposits between basement mebrane and bowman’s layer.

18
Q

What layer does Meesman dystrophy affect?

A

Epithelial

19
Q

What is the histological appearance of Meesman?

A

Irregular thickening of basement membrance of epithelium with tiny intra-epithelial cysts.

20
Q

What are the symptoms of Meesman?

A

Asymptomatic or mild REES with mild blurring

21
Q

Which layer do Reis-Buckler and Thiele-Behnke corneal dystrophy affect?

A

Bowman’s layer

22
Q

What is the histological appearance in Reis-Buckler?

A

Bowman’s layer is replaced by connective tissue bands.

23
Q

What are the symptoms of Reis-Buckler?

A

Reduced sensitivity, reduced vision (can cause severe impairment), severe REES

24
Q

What is the treatment of Reis-Buckler

A

As per REES, mild steroids, PTK works in some patients

25
What are the other names of Thiele-Behnke?
Honeycomb-shaped corneal dystrophy/corneal basement dystrophyt type 2
26
Which is the most severe Reis-Buckler or Thiele-Behnke
Reis-Buckler
27
What is the clinical appearance of Reis-Buckler?
geographic sub-epithelial opacities centrally that increase with age
28
What is the clinical appearance of Thiele-Behnke?
Honeycomb-shaped corneal dystophy
29
Which layer does lattice dystrophy affect?
Stroma
30
Which deposits are involved in lattice dystrophy?
Progressive deposition of amyloid (Amy's lace)
31
Which is the most dangerous subset of lattice degeneration and why?
Type 2 as amyloid is deposited elsewhere
32
What do the deposits in lattice degeneration look like?
Fibre like deposits