7 - Ant Seg Cornea Flashcards
Megalocornea
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
Microcornea
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
Microphthalmos
Small, malformed eye
Diseased
Isolated or with syndromes
Nanopthalmos
Normal small eye (e.g. high hyperopia)
Shallow AC (AACG possible)
Keratoconus
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
Ketaoglobus
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)
Keratoconus vs globus
- etiology
- onset
- location of thinning
- location of protrusion
etiology: both unknown
onset: C puberty, G birth
thinning: C para/central, G generalized
protrusion: C apical, G generalized
Keratoconus vs globus
- scarring
- clinical presentation
- signs
- topography
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
Posterior embryotoxin
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
Peters anomaly
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
Epibulbar/limbal dermoid
- describe
- onset
- contents
- location and size
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
Epibulbar/limbal dermoid
- concerns
- tx
Can induce astig -> amblyopia
Removal for ocular irritation, amblyopia risk
Excision can lead to scarring, astigmatism, amblyopia (i.e. can be worse than before)
Sclerocornea
Total corneal opacification, resembles sclera
Difficult to see limbus
Central K clearer than periphery
Often seen in kids with systemic problems with short lifespan