7 - Ant Seg Cornea Flashcards

1
Q

Megalocornea

A

Non-progressive enlarged cornea
>/= 13mm

Rare, congenital, usually males

XL, AR, or AD
-will be assoc with something/doesn’t occur in isolation

Late assoc with glaucoma, cataracts

Lubrication for exposure keratitis

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2
Q

Microcornea

A

Clear, normal thickness
<9mm newborn, <10mm after 2yrs

AR or AD

Normal globe dimensions

Accompanied with other abnormalities - cataracts, coloboma, cornea plana (flat K), PFV, Ehler-Danlos

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3
Q

Microphthalmos

A

Small, malformed eye
Diseased

Isolated or with syndromes

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4
Q

Nanopthalmos

A

Normal small eye (e.g. high hyperopia)

Shallow AC (AACG possible)

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5
Q

Keratoconus

A

Central/paracenral K bulges, progressive thinning

Presents and progresses into puberty

Hereditary
-down syndrome, atopic disease, chronic eye rubbing

Vogt striae (iron, stress lines) and apical scarring (unlike keratoglobus)
Tears in Descemet’s -> hydrops
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6
Q

Ketaoglobus

A

Bilateral, non-inflamm thinning of entire K

Present at birth, rare, AR

Steep curvature + thinning in periphery, deep AC

Spontaneous breaks in Descemet’s -> acute edema

K rupture with minor blunt trauma (protective eyewear, scleral CLS)

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7
Q

Keratoconus vs globus

  • etiology
  • onset
  • location of thinning
  • location of protrusion
A

etiology: both unknown
onset: C puberty, G birth
thinning: C para/central, G generalized
protrusion: C apical, G generalized

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8
Q

Keratoconus vs globus

  • scarring
  • clinical presentation
  • signs
  • topography
A

scarring: C present, G absent

presentation:

  • C: unilateral, red VA (myop, astig), acute hydrops
  • G: rupture with mild trauma, very rarely acute hydrops

signs:

  • C: conical ectasia, oil drop red reflex, “scissoring” reflex, vogt striae, munson’s sign, fleishers ring
  • G: globular ectasia

topography:

  • C: irreg astig, asymmetric bowtie, skewed radial axis
  • G: generalized steepening
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9
Q

Posterior embryotoxin

A

Aka Prominent Schwalbe’s line

Thickening and anterior displacement of schwalbe’s

Irregular white line ant to limbus, visible on SLE

Isolated finding (10-15% pop) or with Axenfeld-Rieger

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10
Q

Peters anomaly

A

Aka iridocorneal adhesions

Posterior K defect with an overlying stromal opactity with iris strands

  • touching cornea from behind
  • could be the adhesion of the lens to the K

Size/density of opacity ranges
Strands to the defect vary in number, density

Central opacity could get vascularized and protrude

Seen in different diseases, incl Axenfeld-Rieger

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11
Q

Epibulbar/limbal dermoid

  • describe
  • onset
  • contents
  • location and size
A

Fibrofatty tissue covered with epithelium

Present at birth, very little growth after

Could contain ANYTHING - hair follicles, sebaceous/sweat glands, nails

Straddles limbus, could be up to 10mm diameter
Could extend to corneal stroma and adjacent sclera
Mainly inferior limbus

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12
Q

Epibulbar/limbal dermoid

  • concerns
  • tx
A

Can induce astig -> amblyopia

Removal for ocular irritation, amblyopia risk
Excision can lead to scarring, astigmatism, amblyopia (i.e. can be worse than before)

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13
Q

Sclerocornea

A

Total corneal opacification, resembles sclera

Difficult to see limbus

Central K clearer than periphery

Often seen in kids with systemic problems with short lifespan

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