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Clinical Features of glaucoma
Dr.Sidesh Hendavitharana(Registrar-
ophthalmology)
Etiological classification of glaucoma
• primary
– Children
• True congenital glaucoma
• Infantile glaucoma
• Juvenile glaucoma
– Adults
• Primary open angle glaucoma
• Primary angle closure glaucoma
secondary
• Children
– Aniridia
– Iridocorneal dysgenesis
– Ectopia lentis syndrome
– Lowe’s syndrome
– Rubella
• Adults
– Phacogenic glaucoma
– Pigmentary glaucoma
– Pseudoexfoliative glaucoma
– Inflammatory glaucoma
– Neovascular glaucoma
– Ghost cell glaucoma
Clinical features of congenital
glaucoma
• Symptoms
– Photophobia,blepharospasm and eye rubbing due
to irritation of corneal nerves because of elevated
IOP.
– Lacrimation due to corneal edema and erosion.
– Defective vision due to corneal edema leading to
hazy cornea ,enlarment of cornea and eye as a
whole.
– Irritable child.
signs
• Corneal edema(Hazy frosted glass cornea)
– 1st sign to arouse suspicion
– At first,epithelial,lateral stromal
– Results in permanent opacities
• Corneal enlargement
– Along with enlargement of eyeball
– Cornea more than 13mm(normal 10.5mm in infants)
• Tears and breaks in Descemet’s membrane(haab
striae)
– Because of less elasticity
– Appear as horizontal curvilinear lines representing healed
breaks of descemet membrane
.
.
• .
.
• .
.
• Thin and blue sclera(due to stretching of
corneoscleral junction)
• Flattening of lens and backward displacement (due
to stretching of zonules of zinn) and even
subluxation of lens.
• Cupping and atrophy of optic disc especially after
3rd yr
• Raised IOP
• Axial myopia(due to increased in axial length)
anisometropic amblyopia
Clinical features of primary open
angle glaucoma
• Symptoms
– Painless,progressive loss of vision
– Mild headache and eyeache
– Defects in visual fields
– Difficulty in reading and close work(due to failure
in accomodation because of constant pressure on
cilliary muscles and its nerve supply)thus frequent
changes in presbyopic glasses
– Delayed dark adaptation
signs
• Anterior segment
– Normal depth and angle of anterior chamber
– Slightly hazy cornea(late stage)sluggish pupillary
reflex(late stages)
– IOP changes
– In initial stages ,rhythmic swing in diurnal variation of
IOP(morning rise 20%,afternoon rise 25%)
– Variation of >5mm of Hg of IOP is suspicious and
>8mm of Hg is diagnostic
– In late stages, IOP raised permenently above 21
mmHg, usually between 30-45mmHg
Optic disc changes
• Typically progressive and asymetric.
• Pathophysiology
– Mechanical effect
• Raised IOP , forces lamina cribrosa backward
squeezes nerve fibres within its meshes disturbance
in axoplasmic flow
– Vascular factors
• Contribute in ischemic atrophy of nerve fibres resulting
in large caverns or lacunae(cavernous optic atrophy)
Early changes
• Vertically oval cup(due to selective loss of neural rim
tissue in inferior and superior poles)
• Asymetry of cups in both eye(difference more than 0.2)
• Large cup,0.6 or more due to concentric expansion
• Splinter haemorrhage on or near optic disc margin
• Pallor areas on disc
• Atrophy of retinal nerve fiber layer(seen with red free
light)
• Barring of curcumlinear vessels at disc margin
.
• .
.
• .
.
• .
.
• .
.
• .
Advanced changes
• Marked cupping(cup size 0.7-0.9)-bean pot cupping
• Excavation reaching disc margin,steep and no shelving
• Thinning of neuroretinal rim seen as cresentic shadow
adjecent to disc margin on temporal side
• Nasal shifting of retinal vessels with broken off appearance
at margin(bayonetting sign)
• Pulsation of retinal arteries at disc margin
• Pores in lamina cribrosa slit-shaped and visible up to disc
margin(laminar dot sign)
• Glaucomatous optic atrophy
• Destructon of all neural tissue of disc
• Optic nerve head appears white and deeply excavated.
.
• .
.
• .
.
• .
.
• .
Clinical features of ACG
• Symptoms
– Asymptomatic but during attack transient blurring
of vision,coloured halos and mild headache
• Signs
– Eclipse sign
• Shadow on nasal side elicited by shining penlight across
anterior chamber from temporal side
• Indicates decreased axial anterior chamber depth
Slit lamp examination
• Congested episcleral and conjunctival blood
vessels
• Corneal epithelial edema
• Shallow anterior chamber
• Mild amount of aqeous flare and cells
• Mid dilated,sluggish and irregularly shaped pupil
• Convex lens-iris diaphragm
• Glaukomflecken-characteristic small anterior
subcapsular lens opacities
Secondary glaucoma
• Clinical features of neovascular glaucoma
• Symptoms
– Severe pain
– Markedly reduced vision
• Signs
– Ciliary and episcleral congestion
– Corneal edema
– High IOP
– Rubeosis iridis
Causes for NVG
• CREDITS……
• C-CRVO
• R-RD
• E-eale’s disease
• D-diabetic retinopathy
• I-intraocular inflammations
• T-Tumors(intraocular)
• S-sickle cell retinopathy
Pseudoexfoliation syndrome
• Clinical features
– Effects elderly
– Presents like primary open angle glucoma
– Diposition of amorphous grey dandruff like
material on pupillary border,anterior lens
surface,posterior surface of iris,zonules and cilliary
processes
– Arrangement of pigments anterior to schwalbe’s
line-sampaolesi line.
– Subluxation of lens due to looseness of zonules
Clinical features of pigmentary
glaucoma
• Pigment diposition on the corneal endothelium in
a vertical spindle pattern-krukenberg
spindle(absolutely necessary to make the
diagnosis)
• Peripheral iris transillumination-characteristic
spokelike loss of the iris pigment epithelium
• When the pupil is dilated,pigment deposits can
be seen on the zonular fibres,anterior to hyaloid
and the lens capsule near the equator of the
lens(zentmayer line)
THANK YOU
• .

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Clinical features of glaucoma

  • 1. Clinical Features of glaucoma Dr.Sidesh Hendavitharana(Registrar- ophthalmology)
  • 2. Etiological classification of glaucoma • primary – Children • True congenital glaucoma • Infantile glaucoma • Juvenile glaucoma – Adults • Primary open angle glaucoma • Primary angle closure glaucoma
  • 3. secondary • Children – Aniridia – Iridocorneal dysgenesis – Ectopia lentis syndrome – Lowe’s syndrome – Rubella • Adults – Phacogenic glaucoma – Pigmentary glaucoma – Pseudoexfoliative glaucoma – Inflammatory glaucoma – Neovascular glaucoma – Ghost cell glaucoma
  • 4. Clinical features of congenital glaucoma • Symptoms – Photophobia,blepharospasm and eye rubbing due to irritation of corneal nerves because of elevated IOP. – Lacrimation due to corneal edema and erosion. – Defective vision due to corneal edema leading to hazy cornea ,enlarment of cornea and eye as a whole. – Irritable child.
  • 5. signs • Corneal edema(Hazy frosted glass cornea) – 1st sign to arouse suspicion – At first,epithelial,lateral stromal – Results in permanent opacities • Corneal enlargement – Along with enlargement of eyeball – Cornea more than 13mm(normal 10.5mm in infants) • Tears and breaks in Descemet’s membrane(haab striae) – Because of less elasticity – Appear as horizontal curvilinear lines representing healed breaks of descemet membrane
  • 6. .
  • 9. . • Thin and blue sclera(due to stretching of corneoscleral junction) • Flattening of lens and backward displacement (due to stretching of zonules of zinn) and even subluxation of lens. • Cupping and atrophy of optic disc especially after 3rd yr • Raised IOP • Axial myopia(due to increased in axial length) anisometropic amblyopia
  • 10. Clinical features of primary open angle glaucoma • Symptoms – Painless,progressive loss of vision – Mild headache and eyeache – Defects in visual fields – Difficulty in reading and close work(due to failure in accomodation because of constant pressure on cilliary muscles and its nerve supply)thus frequent changes in presbyopic glasses – Delayed dark adaptation
  • 11. signs • Anterior segment – Normal depth and angle of anterior chamber – Slightly hazy cornea(late stage)sluggish pupillary reflex(late stages) – IOP changes – In initial stages ,rhythmic swing in diurnal variation of IOP(morning rise 20%,afternoon rise 25%) – Variation of >5mm of Hg of IOP is suspicious and >8mm of Hg is diagnostic – In late stages, IOP raised permenently above 21 mmHg, usually between 30-45mmHg
  • 12. Optic disc changes • Typically progressive and asymetric. • Pathophysiology – Mechanical effect • Raised IOP , forces lamina cribrosa backward squeezes nerve fibres within its meshes disturbance in axoplasmic flow – Vascular factors • Contribute in ischemic atrophy of nerve fibres resulting in large caverns or lacunae(cavernous optic atrophy)
  • 13. Early changes • Vertically oval cup(due to selective loss of neural rim tissue in inferior and superior poles) • Asymetry of cups in both eye(difference more than 0.2) • Large cup,0.6 or more due to concentric expansion • Splinter haemorrhage on or near optic disc margin • Pallor areas on disc • Atrophy of retinal nerve fiber layer(seen with red free light) • Barring of curcumlinear vessels at disc margin
  • 19. Advanced changes • Marked cupping(cup size 0.7-0.9)-bean pot cupping • Excavation reaching disc margin,steep and no shelving • Thinning of neuroretinal rim seen as cresentic shadow adjecent to disc margin on temporal side • Nasal shifting of retinal vessels with broken off appearance at margin(bayonetting sign) • Pulsation of retinal arteries at disc margin • Pores in lamina cribrosa slit-shaped and visible up to disc margin(laminar dot sign) • Glaucomatous optic atrophy • Destructon of all neural tissue of disc • Optic nerve head appears white and deeply excavated.
  • 24. Clinical features of ACG • Symptoms – Asymptomatic but during attack transient blurring of vision,coloured halos and mild headache • Signs – Eclipse sign • Shadow on nasal side elicited by shining penlight across anterior chamber from temporal side • Indicates decreased axial anterior chamber depth
  • 25. Slit lamp examination • Congested episcleral and conjunctival blood vessels • Corneal epithelial edema • Shallow anterior chamber • Mild amount of aqeous flare and cells • Mid dilated,sluggish and irregularly shaped pupil • Convex lens-iris diaphragm • Glaukomflecken-characteristic small anterior subcapsular lens opacities
  • 26. Secondary glaucoma • Clinical features of neovascular glaucoma • Symptoms – Severe pain – Markedly reduced vision • Signs – Ciliary and episcleral congestion – Corneal edema – High IOP – Rubeosis iridis
  • 27. Causes for NVG • CREDITS…… • C-CRVO • R-RD • E-eale’s disease • D-diabetic retinopathy • I-intraocular inflammations • T-Tumors(intraocular) • S-sickle cell retinopathy
  • 28. Pseudoexfoliation syndrome • Clinical features – Effects elderly – Presents like primary open angle glucoma – Diposition of amorphous grey dandruff like material on pupillary border,anterior lens surface,posterior surface of iris,zonules and cilliary processes – Arrangement of pigments anterior to schwalbe’s line-sampaolesi line. – Subluxation of lens due to looseness of zonules
  • 29. Clinical features of pigmentary glaucoma • Pigment diposition on the corneal endothelium in a vertical spindle pattern-krukenberg spindle(absolutely necessary to make the diagnosis) • Peripheral iris transillumination-characteristic spokelike loss of the iris pigment epithelium • When the pupil is dilated,pigment deposits can be seen on the zonular fibres,anterior to hyaloid and the lens capsule near the equator of the lens(zentmayer line)