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
Q

What are the other names of Thiele-Behnke?

A

Honeycomb-shaped corneal dystrophy/corneal basement dystrophyt type 2

26
Q

Which is the most severe Reis-Buckler or Thiele-Behnke

A

Reis-Buckler

27
Q

What is the clinical appearance of Reis-Buckler?

A

geographic sub-epithelial opacities centrally that increase with age

28
Q

What is the clinical appearance of Thiele-Behnke?

A

Honeycomb-shaped corneal dystophy

29
Q

Which layer does lattice dystrophy affect?

A

Stroma

30
Q

Which deposits are involved in lattice dystrophy?

A

Progressive deposition of amyloid (Amy’s lace)

31
Q

Which is the most dangerous subset of lattice degeneration and why?

A

Type 2 as amyloid is deposited elsewhere

32
Q

What do the deposits in lattice degeneration look like?

A

Fibre like deposits