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INTERSTITIAL
KERATITIS
BALAJI S
Definition
 Non ulcerative inflammation of corneal
stroma without primary involvement of
epithelium and endothelium.
 It is mostly allergic in origin and may be
infective also.
Causes
 Congenital syphilis
 TB
 Cogan’s syndrome
 Acquired syphilis
 Trypanosomiasis
 Leprosy
 Malaria
Syphilitic interstitial
keratitis
CONGENITAL ACQUIRED
More common 90% Less common
Bilateral Unilateral
Age - (5 – 15 ) yrs Any age
Pathogenesis
T.pallidum invades & sensitizes cornea during
foetal stage
later the exposure to either treponema or its toxin
Inflammation of the sensitized cornea due to local
Ag - Ab reaction
symptoms
• Pain
• Lacrimation
• Photophobia
• Blurring of vision
• Blepharospasm
Clinical features
 Hutchinson’s triad – congenital syphilis
Interstitial
keratitis
Hutchinson’s
teeth
Vestibular
deafness
Stages
 Initial progressive stage
 Florid stage
 Stage of regression
Initial progressive stage
• One or more Hazy patches appear in the
deep layers of the stroma.
• Associated with uveitis ( iritis , cyclitis ,
choroiditis )
• Presence of keratic precipitates.
• Diffuse corneal haze – ground glass
appearance
• Lasts for about 2 weeks
Florid stage ( 2 months )
 Deep vascularization of the cornea – radial
bundle of brush like vessels.
 Salmon patch appearance due to the
haziness of cornea.
 May be moderate degree of superficial
vascularization.
 Vessels & conjunctiva appears heaped at
the limbus.
Stage of regression
• Corneal haze resolves slowly & begins
from periphery towards centre.
• As cloudiness disappears , the vessels
become obliterated & they remain
permanently as fine opaque lines ( ghost
vessels ).
• Lasts for about 1 – 2 yrs.
Diagnosis
Corneal haze & other typical findings on
slit lamp examination.
Serology
- VDRL
- T.pallidum immobilisation test
- micro haemagglutination assay
- fluorescent Ab absorption test
Treatment
LOCAL
- topical corticosteroid drops ( 0.1% )
every 2-3 hrs
- atrophine eye ointment 1% 2 – 3
times/day
- dark googles for photophobia
- penetrating keratoplasty
SYSTEMIC
- high doses of penicillin to
prevent further development of lesions
- systemic steroids can be given in
refractory cases.
TB INTERSTITIAL
KERATITIS
 Features similar to syphilitic keratitis
except that it is frequently unilateral &
involves mostly lower sector of cornea.
Treatment
systemic - anti TB drugs
Topical - steroids & cycloplegics
Cogan’s syndrome
• A rare autoimmune disease of eye &
inner ear.
• Common in young adults.
• May be associated with severe vasculitis.
Features
- vertigo , tinnitus & deafness.
- bilateral (IK) , uveitis & blindness.
Treatment
• Urgent evaluation is indicated because
early treatment prevents permanent
deafness & blindness.
• Systemic & topical corticosteroids.
Thank You

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interstitial Keratitis

  • 2. Definition  Non ulcerative inflammation of corneal stroma without primary involvement of epithelium and endothelium.  It is mostly allergic in origin and may be infective also.
  • 3. Causes  Congenital syphilis  TB  Cogan’s syndrome  Acquired syphilis  Trypanosomiasis  Leprosy  Malaria
  • 4. Syphilitic interstitial keratitis CONGENITAL ACQUIRED More common 90% Less common Bilateral Unilateral Age - (5 – 15 ) yrs Any age
  • 5. Pathogenesis T.pallidum invades & sensitizes cornea during foetal stage later the exposure to either treponema or its toxin Inflammation of the sensitized cornea due to local Ag - Ab reaction
  • 6. symptoms • Pain • Lacrimation • Photophobia • Blurring of vision • Blepharospasm
  • 7. Clinical features  Hutchinson’s triad – congenital syphilis Interstitial keratitis Hutchinson’s teeth Vestibular deafness
  • 8.
  • 9. Stages  Initial progressive stage  Florid stage  Stage of regression
  • 10.
  • 11. Initial progressive stage • One or more Hazy patches appear in the deep layers of the stroma. • Associated with uveitis ( iritis , cyclitis , choroiditis ) • Presence of keratic precipitates. • Diffuse corneal haze – ground glass appearance • Lasts for about 2 weeks
  • 12.
  • 13.
  • 14. Florid stage ( 2 months )  Deep vascularization of the cornea – radial bundle of brush like vessels.  Salmon patch appearance due to the haziness of cornea.  May be moderate degree of superficial vascularization.  Vessels & conjunctiva appears heaped at the limbus.
  • 15.
  • 16. Stage of regression • Corneal haze resolves slowly & begins from periphery towards centre. • As cloudiness disappears , the vessels become obliterated & they remain permanently as fine opaque lines ( ghost vessels ). • Lasts for about 1 – 2 yrs.
  • 17.
  • 18. Diagnosis Corneal haze & other typical findings on slit lamp examination. Serology - VDRL - T.pallidum immobilisation test - micro haemagglutination assay - fluorescent Ab absorption test
  • 19. Treatment LOCAL - topical corticosteroid drops ( 0.1% ) every 2-3 hrs - atrophine eye ointment 1% 2 – 3 times/day - dark googles for photophobia - penetrating keratoplasty
  • 20. SYSTEMIC - high doses of penicillin to prevent further development of lesions - systemic steroids can be given in refractory cases.
  • 21. TB INTERSTITIAL KERATITIS  Features similar to syphilitic keratitis except that it is frequently unilateral & involves mostly lower sector of cornea. Treatment systemic - anti TB drugs Topical - steroids & cycloplegics
  • 22. Cogan’s syndrome • A rare autoimmune disease of eye & inner ear. • Common in young adults. • May be associated with severe vasculitis. Features - vertigo , tinnitus & deafness. - bilateral (IK) , uveitis & blindness.
  • 23.
  • 24. Treatment • Urgent evaluation is indicated because early treatment prevents permanent deafness & blindness. • Systemic & topical corticosteroids.