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7/29/2019 Corneal Dystropies http://slidepdf.com/reader/full/corneal-dystropies 1/4 Lineses, Pamela Louise M. Ocular Disease I ODP-2A CORNEAL DYSTROPHIES CORNEAL DYSTROPHIES  SIGN SYMPTOM  COMMON MANAGEMENT/ TREATMENT  1. Epithelial Dystrophies  1.1. Juvenile Epithelial Dystrophy (of Meeshman) 1.2. Recurrent Corneal Erosion 1.3. Epithelial Basement Membrane Dystrophy clear dot or cyst in the corneal epithelium that occasionally ruptures) photophobia lacrimation Recurrent corneal Erosion often follows an uncomplicated corneal abrasion Examination indicates a corneal are denuded of epithelium minute opacities corneal epithelial cell form an ever- changing subtle pattern of minor opacites describe as map-dot- fingeprint, bleblike or microcystic mild irritation slight decrease in clarity of vision (visual acuity) Severe , sharp ocular pain upon awakening most patients are assymptomatic ubless recurrent corneal erosion occurs   Treatment is solely symptomatic patching instillation of petrolatum oinment (prevention of eyelid tio adhere to corneal epithelium) minute puncture of the basement membrane with fine curve needle or Nd: Yag Laser nighttime lubricating ointments or hypertonic saline ointments

Corneal Dystropies

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Page 1: Corneal Dystropies

7/29/2019 Corneal Dystropies

http://slidepdf.com/reader/full/corneal-dystropies 1/4

Lineses, Pamela Louise M. Ocular Disease I

ODP-2A

CORNEAL DYSTROPHIES 

CORNEAL

DYSTROPHIES   SIGN SYMPTOM  COMMON 

MANAGEMENT/ 

TREATMENT  

1. Epithelial 

Dystrophies  

1.1. Juvenile

EpithelialDystrophy (of Meeshman)

1.2. RecurrentCornealErosion

1.3. EpithelialBasementMembraneDystrophy

● clear dot or cyst in

the cornealepithelium thatoccasionallyruptures)

● photophobia● lacrimation

● Recurrent cornealErosion

● often follows anuncomplicatedcorneal abrasion

Examinationindicates a cornealare denuded of epithelium

● minute opacities

● corneal epithelialcell form an ever-changing subtlepattern of minor opacites describe

as map-dot-fingeprint, bleblikeor microcystic

● mild irritation●

slight decrease inclarity of vision(visual acuity)

● Severe , sharpocular pain uponawakening

● most patients areassymptomaticubless recurrentcorneal erosionoccurs

 

● ●

Treatment is solelysymptomatic

● patching● instillation of 

petrolatum oinment(prevention of 

eyelid tio adhere tocorneal epithelium)●minute puncture of 

the basementmembrane withfine curve needle or Nd: Yag Laser 

● nighttime lubricatingointments or hypertonic salineointments

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2. Bowm an Layer 

Dystrophies 

2.1.Reis-Bucher Central corneal

dystrophy

2.2. Thiel-BehnkeDystrophy(Honey Comb)

● ring shaped,superficial opacity in

the central cornea● corneal erosion that

gradually cease atthe center of thecore

● Typical honeycombopacity in thecornealsubepithelium regiondevelops in thesecond decade of life

● pain● photophobia●

foreign bodysensation● reduce visual acuity● irregular 

astigmatismcombined withcornealopacification

● recurrent painfulerosions

● decreased vision

● Superficialkeratectomy may

help with thesuperficial cornealscarring

● lamellar Keratoplasty

● excimer laser keratectomy

● In more severecases, a partial or complete cornealtransplantation maybe considered

● 

3. Strom al 

Dysthrophies 

3.1. Central MaculaDystrophy(Groenouwtype II)

3.2. lattice cornealDystrophy

● begins in childhoodas a diffuse cloudingand progres untilentire thickness of cornea contains grayspot

● recurrent erosionmay occur 

● characterized by thedevelopment of lesions that formbranching lines thatresemble cracked

● pain due torecurrent erosion

● pain

● penetratingkeratoplasty

● keratoplasty● corneal transplant● excimer laser 

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3.3. Granular CornealDystrophyType I

3.4. Granular CornealDystrophyType II

3.5. Schnyder CrystallineCornealDystrophy

glass or thecrisscrossed,overlapping patternof lattice

● corneal opacities

● small particles(granules) thatcollectively resemblebreadcrumbs(develops in secondor third decade of life)

● lesion combines toform larger lesion

● recurrent cornealerosion can occur 

● develop on thestroma usuallybeginning in the firstor second decade of life

● opacities in thecornea

● superficial, fineopacities thatresemble rings,discs, stars or snowflakes mostdense centrally 

● opaque corneas dueto an accumulationof fat or cholesterol

● Central, oval ,subepithelialcrystalline opacity

●Diffuse cornealhaze, prominentcorneal arcus

● 

● pain

● 

● clouding, hazinessand blurred vision

● Visual impairment,glare

● penetratingkeratoplasty

● Treatment- usuallynot required

● Excimer laser keratectomy.

● corneal transplantmay be indicate

● 

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4. Endothelial 

Dystrophies 

4.1. FuchsEndothelial

Dystrophy

4.2. Posterior PolymorphousDystrophy

4.3. CongenitalHereditaryEndothelialDystrophy

● develops duringmiddle age, bilateral

condition●warthlike excresence● Tiny blisters form on

the cornea● endematous cornea

● characterizeddescemetmembrane withlocalized excerences

● endothelial cellsresembles fibroblastor epithelial cells

● opacity

● bilateral symmetricaldiffuse cornealedema

● blue gray groundglass appearance tototal opacification

● pain● reduce vision

● often asymptomatic

● pain

● hypertonic saline or glucose solution

dehydrate theedematous corneaand may improvevision

● Corneal transplant if impairment of visionoccurs

● not required

● sodium chloridedrops, in attempt toreduce the cornealswelling 

● cornealtransplantation,may be considered.