Corneal Degeneration and Ectasia Flashcards

1
Q

What is degeneration?

A

A process in which normal elements of corneal tissue are converted representing a change in tissue

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2
Q

Degeneration could be due to ______ and _______

A

Involution and metabolic disease

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3
Q

The change in tissue that occurs with degeneration could be _____ or _____

A

benign or detrimental to normal physiology

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4
Q

Describe the ongoing process in the photo

A

Epithelial Cell migration

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5
Q

What are the non sight threatening corneal degenerations?

A
  • Crocodile Shagreen (mosaic)
  • Arcus Senilis
  • Limbal Girdle of Vogt
  • Farinata
  • Terrien’s Marginal Degeneration
  • Mooren’s Ulcer
  • Amyloid
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6
Q

What are the sight threatening opacifying corneal degenerations?

A
  • Salzmann’s Nodular
  • Amyloid
  • Spheroidal
  • Band Keratopathy
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7
Q

What is the condition indicated in the photo?

A

Crocrodile Shagreen

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8
Q

What is the significance in the finding of arcus in a patient < 40yrs old?

A

The patient most likely has hyperlipidemia

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9
Q

What condition is presented in the photo?

A

Arcus

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10
Q

Describe the conditions portrayed in the pictures

A
  • Anterior crocrodile shagreen: at the level of Bowman’s layer
  • Posterior crocodile Shagreen: at the posterior corneal stroma & Descemet’s
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11
Q

How many types of Limbal Girdle of Vogt are there?

A

Two

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12
Q

Describe Type I Limbal Girdle of Vogt

A
  • Lucid interval – deposition ends at Bowman’s. Swiss cheese holes. Sharp edge centrally
  • Early form of band keratopathy
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13
Q

Describe Type II Limbal Girdle of Vogt

A

“True Vogt’s”
•To limbus – elastoid degeneration of subepithelial collagen. Extensions centrally

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14
Q

Describe the condition in the photo

A

Limbal Girdle of Vogt

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15
Q

ID the condition in the photo and specify which category

A

Type 1 Limbal Girdle of Vogt

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16
Q

ID what condition is in the picture and specify which category it is

A

Type 2 limbal Girdle of Vogt

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17
Q

What are farinata?

A

white dust-like particles
pre-Descemet’s
with aging

18
Q

Furrow Degeneration refers to ____

A

painless, noninflammatory peripheral corneal thinning, adjacent to corneal arcus that occur without vascularization

19
Q

Stocker’s line

A

Refers to the occasional line of iron deposition can be seen adjacent to the head of the pterygium

20
Q

Describe the boxed feature in the photo

A

Stocker’s line

21
Q

ID the highlighted feature in the photo

A

Hudson-Stahli line

22
Q

ID the features in the photo

A

Iron lines

23
Q

ID the condition in the photo

A

Terrien’s Marginal Degeneration

24
Q

ID the condition in the photo

A

Terrien’s Marginal Degeneration

25
What is a differential diagnosis for Terrien's Marginal Degeneration?
Mooren's Ulcer
26
Terrien's Marginal Degeneration usually occurs in which geographic region?
Superior region
27
Terrien's is not a perforating disease. T/F
T | (Epithelium is intact)
28
List some charax of Terrian's Marginal Degeneration
* bilateral * thinning of peripheral corneal stroma starts superior-nasal then circumferential * fine line of lipid deposit * marginal opacification with superficial vascularization * males \>\> females * any age and \>40
29
What conditions are indicated in the photos?
Vascularization and pseudo-pterygium due to Terrien's
30
Describe the condition in the picture and indicate its common charax
non-infectious, unknown etiololgy (most likely autoimmuned)
31
what are the symptoms associated with Mooren's
Photophobia, red eye, pain
32
What are the signs of Mooren's?
* disrupted corneal epithelium near limbus * typically progressive (circumferentially and centrally) * thinning, stromal melting, potentially perforation
33
what staining method is used to examine Mooren's?
NaFl staining
34
What are the types of Mooren's?
* Type I: typically seen in the older patient, unilateral, better response to treatment * Type II: younger (African descent) 20-30 yr old, bilateral, poor response to treatment
35
How would you differentiate Mooren's from Terrien's?
* Terrien’s epithelium intact, no NaFl stain (not true ulceration) * Terrien’s rarely painful, inflammatory * Terrien’s rarely aggressive * Terrien’s rarely move centrally * Terrien’s rarely perforates
36
What is the systemic disease workup for Mooren's?
•Mandatory referral for vasculitis or collagen vascular disease Autoimmune disease
37
What is the treatment for Mooren's?
supportive treatment with topical steroids to control inflammation •Conjunctival resection, radiation •Bandage CL •Topical cyclosproine or systemic immunosupression •Perforation: tx with cyanoacrylate or lamellar keratoplasty
38
ID the condition in the photo and indicate some of its charax
Polymorphic Amyloid Degeneration Deep stromal, bilateral and similar to Lattice Dystrophy
39
ID the condition in the photo
Spheroidal Degeneration
40
ID the conditin in the photo
Salzmann's Nodular degeneration
41