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Pigmentations

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Less serious degeneration's


Arcus

  • Stromal
  • Clear band at limbus
  • Check lipids if under 50
  • Check carotids if unilateral

Coats white ring

  • White ring around area of previous foreign body

Dellen 

  • "Gaule spot"
  • "Fuchs dimples"
  • Depression of  cornea at 3:00 and 9:00 next to a raised mass
  • Localized dehydration of top 3 layers of cornea
  • Hay fever, conjunctivitis, ptyrgium, scleritis, blebs, sutures


Hassle - Henle bodies 

  • "Decemets warts"
  • Small round thickenings of Decemets membrane at periphery
  • "Peripheral guttata"

Marginal furrow

  • Bilateral thinning at limbus
  • No inflammation and no problem

Posterior crocodile shagreen

  • Diffuse gray polygonal degeneration of posterior cornea

Spheroid  degeneration

  • Keratinoid
  • Oily appearing subepithelial droplets

White girdle of Vogt

  • 50+ females
  • Bilateral narrow band of fine crystal yellow - white  opacities
  • Along nasal or temporal limbus

Foreign bodies

  • Deep rust may rise to surface with time
  • Hole will fill-in in 24-48 hr's
  • Edema ring will disappear in 48-72 hr's
  • Traumatic iridocyclitis may occur 24-36 hr's after injury and should subside after re-epithelialization
  • If Bowmans membrane is damaged scarring will result

Keratoconjunctivitis

  • Acute pain or foreign body sensation without injury or irritation
  • Superficial erosions
  • Microcystic edema
  • Punctate infiltrates
  • Superficial pannus 
  • Deeper neovascularization
  • Dendritic ulceration - H Simplex and H Zoster
  • Infiltrative keratitis  is usually epithelial and non-infectious.  Usually a focal response (Staph?)
  • Sub-epithelial infiltrate usually indicates virus
  • If it leaves a scar it must have been deep?  Likely viral
  • Ulcerative keratitis is usually stromal and infectious

Membranes

  • Pseudo-membrane on top of conjunctiva
  • True membrane fibrin fibers interdigitates with epithelium and will bleed on removal

Lymph nodes

  • Swelling indicates viral or sever bacterial infection

Palpable, not tender, not visable

  • PCF
  • Chlamydia
  • Newcastle
  • Enterovirus 70

Palpable, tender, non-visable

  • EKC
  • Herpes
  • Pre-septal cellulitis

Palpable, tender, grossly visable

  • Oculoglandular syndrome
  • Tuberculosis
  • Sarcoid
  • Severe EKC
  • Infectous granulomatous disease

Seasonal variation
Strept pneumonia most common in winter in the north-east US
H. flu most common in summer and fall in south-east US

Problem degeneration's    

Amyloid degeneration

  • Deposits following long-standing disease

Anterior keratoconus

  • First sign at 15-25
  • Progresses for 6 yrs
  • Allergies and frequent eye-rubbers
  • Autosomal recessive
  • Stromal thinning
  • Ruptures in Decemets membrane
  • Distorted mires on keratometer
  • Fit with contact lenses
  • Munsons sign on downgaze

Band keratopathy

  • Bilateral whitish - yellow haze (calcium) in epithelium and bowmans
  • "Swiss cheese" appearance to intrapalpebral cornea
  • Decreased acuity
  • Foreign body sensation
  • Lubricate and check parathyroid gland
  • Causes
    •    Sarcoid
    •    Hyperparathyroid
    •    Vitamin D toxicity
    •    Multiple myeloma
    •    Renal failure
    •    Hyper or hypophosphatemia
    •    Long standing inflammatory conditions (Arthritis),
    •    Chronic topical medications preserved with mercury

Bullous keratopathy

  • #1 cause is post operative
  • #2 cause is Fuchs endothelial dystrophy
  • #3 cause is result of endothelial cell loss over lifetime
  • Before bullae form treat with antiedema therapy
  • If bullae soft lens bandage and antibiotics
  • Eventual painful fibrotic blind cornea

Cogans degeneration

  • Older males develop large 1-2 mm peripheral microcysts
  • Treat RCE

Essential iris atrophy

  • 30-40 white females
  • Unilateral anterior synechia leads to atrophy and glaucoma

Keratoconjunctivitis sicca (KCS)

  • Filimentary keratitis
  • lip and tongue ulcers, caries
  • Tears 
    • Lipid layer Meibomian and Zeiss
    • Aqueous   Lacrimal, Krause Wolfring
    • Mucin        Goblet cells
  • Dry eyes:
    • Lipid abnormalities
      • Blepharitis
      • Bacteria break down lipid into free fatty acids
      • Lid scarring
    • Aqueous deficiency (KCS)
      • Hereditary congenital alacrima
      • Hypoplasia of lacrimal gland
      • Sjogrens syndrome

        90% Female
        Dry eyes, dry mouth, connective tissue disease
        Lymphoid infiltration and destruction of lacrimal and salivary glands

    • Mucin deficiency
      • Hypovitaminosis A
      • Steven Johnson
      • Trachoma
      • Burns
      • Lid surface abnormality
      • Nocturnal lagophthalmos
      • 7th nerve paralysis
    • Dry eye tests
      • Rose bengal - best test
      • BUT < 10 (actually a test of lipids)
      • Shirmer test - Normal is 10-30 mm
        • Test 1 - Measures reflex + base tearing
          Positive if <5 mm
        • Test 2 - Anesthetize cornea and irritate nasal mucosa for 10 sec
          measures only base tearing
          Positive if <15 in 2 minutes
           
        • Lysozyme
        • Lactoferrin
        • Impression cytology
        • Tear osmolarity

Moorens ulcer

  • White - gray infiltrates and  conjunctival  hyperemia causes breakdown of epithelium and degeneration of anterior stroma leading to central overhang
  • Peripheral serpiginous ulcer (Fungal?)
  • No discharge
  • Two forms
  • Unilateral in older patient          - responds well
  • Bilateral in 20-40 yr old patient - responds poorly
  • Most lateral to medial

    Differentiation:
    Marginal furrow is painless
    Pellucid is inferior
    Terriens is superior

Pellucid marginal degeneration

  • Age 20-40
  • Bilateral inferior corneal thinning (80%)
  • Epithelial and endothelium normal
  • Bowmans membrane missing
  • Decemets folded
  • Increased against the rule astigmatism
  • May be a form of keratoconus

Pemphigoid

  • Mainly females
  • Onset usually 60-70
  • Keratinization, shrinkage, scarring
  • Ectropian
  • Ptyrgia
  • Blebs
  • Epitheliopathy
  • Herpetic scarring
  • Vth nerve damage
  • Persistent edema


Recurrent erosions

  • 50% have EBMD
  • Surgical trauma
  • Vitreous touch of intact vitreous face
  • Trauma

Rupture of  decemets membrane

  • Forceps delivery
  • Congenital glaucoma

Salzmans nodular degeneration

  • Elevated blue - gray nodules of hypertrophic collagen on periphery
  • Between epithelium and bowmans membrane
  • RCE
  • More often women


Terriens marginal degeneration

  • Age 20-50 males
  • Progressive
  • Non-inflammatory
  • Unilateral superior nasal thinning of stroma 
  • Epithelium remains intact
  • Fine vascular pannus across area of thining
  • Leads to scarring, neovascularization and astigmatism
  • Treat with steroids
  • Increased against the rule astigmatism
 

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Copyright © 1997, 1998, 1999, 2000, 2001, 2002, 2003, 2004, 2005, 2006 Don Steensma, O.D., F.A.A.O.
Last modified: May 1, 2006