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CORNEAL DEGENERATIONS
1. Age-related
• Arcus senilis
• Vogt white limbal girdle
2. Lipid keratopathy
• Crocodile shagreen
• Cornea guttata
• Primary
• Secondary
3. Band keratopathy
4. Spheroidal degeneration
5. Salzmann nodular degeneration
Arcus senilis
• Innocuous and extremely common in elderly
• Occasionally associated with hyperlipoproteinaemia
• Bilateral, circumferential bands
of lipid deposits
• Diffuse central and sharp
peripheral border
• Peripheral border separated
from limbus by clear zone
• Clear zone may be thinned
( senile furrow)
Vogt white limbal girdle
• Innocuous and very common in elderly
• Bilateral
• White, crescentic line along nasal and temporal
limbus
• Type 1 - separated from limbus by clear zone
• Type 2 - not separated by clear zone
Crocodile shagreen
• Uncommon and innocuous
• Usually bilateral
• Polygonal stromal opacities separated by
clear space
• Most frequently involve anterior stroma
(anterior crocodile shagreen)
• Occasionally involve posterior stroma
(posterior crocodile shagreen)
Cornea guttata
• Common, bilateral and usually innocuous
• Rarely progression to Fuchs dystrophy
• Tiny dark spots on central endothelium
• Similar peripheral lesions are Hassell-Henle bodies
Lipid keratopathy
• Usually unilateral stromal deposits
without vascularization
• Rare, occurs spontaneously in
avascular cornea
• Unilateral stromal deposits with
vascularization
• Common, secondary to previous
disciform keratitis
Treatment - coagulation of feeder
vessels and/or keratoplasty
Treatment - keratoplasty, if severe
Primary Secondary
Band keratopathy
• Interpalpebral limbal opacification
• Common, unilateral or bilateral depending on cause
• Subepithelial calcification
• Central spread of calcification
• Small holes within calcified area
• Separated by clear zone
Progression
Causes of Band Keratopathy
1. Ocular (common)
• Silicone oil in anterior chamber
• Increased serum calcium and phosphorus
• Chronic iridocyclitis, particularly in children
• Hyperuricaemia
• Associated with phthisis bulbi
3. Hereditary (rare)
• Chronic renal failure
• Familial band keratopathy
• Hereditary ichthyosis
2. Metabolic (rare)
4. Age-related (uncommon)
Removal of corneal epithelium Application of sodium versenate
Chelation of band keratopathy
Spheroidal degeneration
Treatment
Central spread, coalescence and
opacification
Advanced lesions become
nodular and elevated
• Rare, typically affects outdoor workers
• Starts with peripheral, interpalpebral, small amber-coloured
granules in superficial stroma
• Debridement or superficial keratotomy if mild
• Keratoplasty if severe
Progression
Salzmann nodular degeneration
• Uncommon, unilateral or bilateral
• Secondary to chronic keratitis
• Discrete superficial stromal opacities
and nodules
• Base of nodule may be surrounded by
iron deposits
Treatment - similar to spheroid degeneration

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16Corneal Degenerations.ppt

  • 1. CORNEAL DEGENERATIONS 1. Age-related • Arcus senilis • Vogt white limbal girdle 2. Lipid keratopathy • Crocodile shagreen • Cornea guttata • Primary • Secondary 3. Band keratopathy 4. Spheroidal degeneration 5. Salzmann nodular degeneration
  • 2. Arcus senilis • Innocuous and extremely common in elderly • Occasionally associated with hyperlipoproteinaemia • Bilateral, circumferential bands of lipid deposits • Diffuse central and sharp peripheral border • Peripheral border separated from limbus by clear zone • Clear zone may be thinned ( senile furrow)
  • 3. Vogt white limbal girdle • Innocuous and very common in elderly • Bilateral • White, crescentic line along nasal and temporal limbus • Type 1 - separated from limbus by clear zone • Type 2 - not separated by clear zone
  • 4. Crocodile shagreen • Uncommon and innocuous • Usually bilateral • Polygonal stromal opacities separated by clear space • Most frequently involve anterior stroma (anterior crocodile shagreen) • Occasionally involve posterior stroma (posterior crocodile shagreen)
  • 5. Cornea guttata • Common, bilateral and usually innocuous • Rarely progression to Fuchs dystrophy • Tiny dark spots on central endothelium • Similar peripheral lesions are Hassell-Henle bodies
  • 6. Lipid keratopathy • Usually unilateral stromal deposits without vascularization • Rare, occurs spontaneously in avascular cornea • Unilateral stromal deposits with vascularization • Common, secondary to previous disciform keratitis Treatment - coagulation of feeder vessels and/or keratoplasty Treatment - keratoplasty, if severe Primary Secondary
  • 7. Band keratopathy • Interpalpebral limbal opacification • Common, unilateral or bilateral depending on cause • Subepithelial calcification • Central spread of calcification • Small holes within calcified area • Separated by clear zone Progression
  • 8. Causes of Band Keratopathy 1. Ocular (common) • Silicone oil in anterior chamber • Increased serum calcium and phosphorus • Chronic iridocyclitis, particularly in children • Hyperuricaemia • Associated with phthisis bulbi 3. Hereditary (rare) • Chronic renal failure • Familial band keratopathy • Hereditary ichthyosis 2. Metabolic (rare) 4. Age-related (uncommon)
  • 9. Removal of corneal epithelium Application of sodium versenate Chelation of band keratopathy
  • 10. Spheroidal degeneration Treatment Central spread, coalescence and opacification Advanced lesions become nodular and elevated • Rare, typically affects outdoor workers • Starts with peripheral, interpalpebral, small amber-coloured granules in superficial stroma • Debridement or superficial keratotomy if mild • Keratoplasty if severe Progression
  • 11. Salzmann nodular degeneration • Uncommon, unilateral or bilateral • Secondary to chronic keratitis • Discrete superficial stromal opacities and nodules • Base of nodule may be surrounded by iron deposits Treatment - similar to spheroid degeneration