Signs, Symptoms, and Tx Flashcards

1
Q

What is the Tx for corneal hydrops?

A

Cycloplegic (cyclopentolate 1%) Bacitracin ointment q.i.d. Consider brimonidine 0.1% b.i.d. OR Sodium chloride 5% ointment b.i.d. until resolved

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2
Q

What is the typical follow up schedule for corneal hydrops?

A

1-4 weeks

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3
Q

Describe typical corneal dystrophy properties.

A

Bilateral Inherited (usually AD - Except macular dystrophy and type 3 lattice dystrophy Progressive Without inflammation No corneal neo

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4
Q

What are the 3 anterior corneal dystrophies?

A

EBMD (Map-dot-fingerprint) Meesmann Corneal dystrophy of Bowman’s layer Reis-Buckler (type 1); Thiel-Behnke (type 2)

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5
Q

Which is the most common anterior corneal dystrophy?

A

EBMD

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6
Q

When is Meesmann Dystrophy typically noted?

A

The first years of lief, but asymptomatic until middle age

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7
Q

What are the typical findings of EBMD?

A

Diffuse gray patches (maps) Creamy white cysts (dots) Fine refractile lines (fingerprints)

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8
Q

What symptoms are associated with EBMD?

A

Corneal erosions - like RCE Decreased VA Monocular diplopia Shadow images

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9
Q

What is the typical finding in Meesmann dystrophy?

A

Discrete, tiny epithelial vesicles diffusely involving the cornea, but concentrated in the palpebral fissure

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10
Q

What Tx is common in Meesmann?

A

None, but if severe photophobia or reduced VA occurs, bandage SCls or superficial keratectomy may be beneficial

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11
Q

Meesmann dystrophy is a dystrophy of which layer of the cornea?

A

Epithelium

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12
Q

Reis-Bucklers is a dystrophy of which corneal layer?

A

Bowman’s

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13
Q

When does Reis-Buckler typically appear?

A

Early in life

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14
Q

What are the typical findings in Reis-Buckler?

A

Subepithelial, gray reticular opacities in the central cornea

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15
Q

What are the common symptoms of Reis-Buckler?

A

Recurrent corneal erosions Reduced VA

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16
Q

What are the common Txs for Reis-Buckler?

A

Corneal transplantation surgery - but dystrophy may recur Excimer laser PTK or superficial lamellar keratectomy may work

17
Q

What are the 4 stromal dystrophies?

A

Lattice Granular Macular Schnyder

18
Q

What is the common Tx for stromal dystrophies that are causing reduced VA?

A

Corneal transplant or PTK

19
Q

Dx?

A

Reis Buckler Epithelial dystrophy

20
Q

Dx?

A

Reis Buckler Epithelial Dystrophy

21
Q

Dx?

22
Q

Dx?

23
Q

Dx?

24
Q

Dx?

A

Meesmann Epithelial dystrophy

25
Dx?
Meesmann Epithelial dystrophy
26
Dx?
Meesmann Epithelial dystrophy
27
Dx?
Lattice Stromal dystrophy
28
Dx?
Lattice Stromal dystrophy
29
How many clinical forms of Lattice Stromal dystrophy exist?
4
30
What is the most common form of Lattice Stromal dystrophy?
Type 1 - Biber-Haab-Dimmer
31
What are the common findins of type 1 Lattice Stromal dystrophy?
Refractile branching lines White subepithelial dots Scarrig of the central cornea (on retro)
32
What is one of the common complaints with Lattice Stromal dystrophy?
RCE
33
On which part of the cornea does Lattice Stromal dystrophy typically present?
Central - periphery is usually clear
34
What is the Tx for RCE?
Acute: Cycloplegic (ex 1% cyclo) and ABx ointment (erythromycin or bacitracin 4-6x daily) Post healing: ATs 4-8x daily for 3-6mo; or Muro128 4x daily for 3-6mo
35
What is type 2 Lattice Stromal dystrophy associated with?
Systemic amyloidosis Facial mask Ear abnormalities Cranial and peripheral nerve palsies Dry and lax skin
36
When is the typical onset of types 3 and 4 Lattice Stromal dystrophy?
5-7th decades