Disorder of Vision

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61 Terms

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Aqueous humor pathway

Made by ciliary body EP → travel through posterior chamber → enter anterior chamber → 90% enter trabecular meshwork → Canal of Schlemm → episcleral vss; 10% drain into uvea and sclera

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Parts of accommodation

Lens accommodation by zonule tension/relaxation, miosis, convergence

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Cellular eye layers

Outer = choroid → pigmented EP → rod and cone → Outer nuclear → outer plexiform → inner nuclear → inner plexiform → ganglion cell layer → nerve fiber layer → nearest to vitreous humor

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Vascular supply of the occipital cortex

PCA from basilar supplies the medial part of occipital; MCA from ICA supplies the lateral part of occipital

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Vascular supply of the eye

ICA clinoid → Opthalmic A → Central retinal that pierce and feed center of eye + posterior ciliary a → short is near optic disc, long supplies ciliary muscle

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What part of the eye is spared when there is infarction of retinal supply

Foveola only

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Pupillary light reflex pathway

Light enter optic nerve → signal branch out (one cross chiasm one doesn’t) → optic tract → synapse at pretectal area in LGN → Bilat projection into Edinger-Westphal → travel along CN III → synapse at ciliary ganglion → miosis

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Mechanisms of reduced vision (non nerve)

Refractive area = light is not doing into retina

Media opacity = light is obstructed bc media is cloudy

Retina = photoreceptor and structures fail

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What are refractive errors

Simple bad eyesight fixed with glasses

Myopia → light does not reach retina → fix w concave lens

Hyperopia → light extends past retina → fix w convex lens

Astigmatism → many light refractions → fix w circular lens

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What is presbyopia

Impaired accommodation in older people from loss lens elasticity, change in lens curvature and lower ciliary muscle strength

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What is pinguecula and pterygium

Fibrovascular growth of conjuctiva

  • Pinguecula → does NOT involve limbus

  • Pterygium → grows big enough to reach into cornea causes astigmatism


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<p>What is the difference between these two images</p>

What is the difference between these two images

Lt → has not reached limbus = pinguecula → likely no vision problem

Rt → crosses limbus to cornea = pterygium → expect astigmatism

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Causes of corneal ulcer and scar

Infection (HSV), SJS, Reiter, corneal edema/deposition, keratitis, glaucoma, trauma

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What are cataracts

INCREASED opacity of the lens

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<p>What is the difference between these 3 types of cataracts</p>

What is the difference between these 3 types of cataracts

Lt → See orange center = senile nuclear

Middle → See white fibers in center with some clear area → Cortical

Rt → white fiber with NO clear area → Mature cortica

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<p>What is this</p>

What is this

Fully opaque lens and brown deposits at the bottom of lens → Margagnian cataract

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Component of glaucoma

Loss of retinal ganglion cell, cupping, visual field defect

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What is glaucoma

Change in aqueous humor flow → eg flow of trabecular meshwork = lack of outflow into vss

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What is the difference between primary and secondary open angle glaucoma

Primary (POAG) → more frequent in older and black people

Secondary (SOAG) → RBC/WBC etc block trabecular network → higher episcleral venous pressure

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Signs of angle closure glaucoma

EMERGENCY → painful red eye, sudden vision loss, halo around light, headache, fixed dilate pupil, nausea vomiting

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Types of uvea abnormalities

Keratic precipitate, hypopyon (cell that settle at the bottom), vitritis (blurred optic disc), neuroretinitis (cat scratch, see macular star)

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What is diabetic retinopathy

Non proliferative DR → damaged capillary leak of blood/lipid/macular edema

Proliferative DR → chronic hypoxia → neovascular formation → retinal traction

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<p>What are the abnormalities found in DR</p>

What are the abnormalities found in DR

Green = hard exudate

Purple = microaneurysm

Blue = dot/blot hemorrhage

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<p>What is this</p>

What is this

Blood in vitreous humor → rupture of ciliary/retinal vss

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<p>Seeing this with increased frequency is a sign of what</p>

Seeing this with increased frequency is a sign of what

If you see floaters infrequently is benign → if increased is sign of vitreous detachment common in DM w neovascularization

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Types if retinal detachment

- Rhegmatogenous retinal detachment (RRD): retinal breaks

- Tractional retinal detachment (TRD): DR

- Exudative retinal detachment: Uveitis, mass

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What is hypertensive retinopathy

Chronic uncontrolled HTN → causes endothelial disruption, fibrinoid necrosis and retinal damage

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<p>What are all these signs</p>

What are all these signs

Signs of HYPERTENSIVE RETINOPATHY

Blue = Arterial narrowing

Red = Arteriovenous (AV) nicking

Pink = Cotton wool spots

Can also present with: Flame-shaped retinal hemorrhages, Microaneurysms, Optic nerve head swelling

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What is central retinal artery occlusion (CRAO)

Acute painless monocular vision loss → see retinal WHITENING with CHERRY RED fovea

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<p>What is this</p>

What is this

CRAO → white retina + cherry red fovea

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What is BRAO

Occlusion of a BRANCH of central retina → whitening only in area that branch supplies

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<p>Diff these two images</p>

Diff these two images

Lt = CRAO → retina is white and general + cherry red fovea

Rt = BRAO → partial white retinal area

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What is amaeurosis fugas

Sudden painless vision loss → curtain linked lasting a few seconds → completely back to normal → caused by TIA

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<p>What is this</p>

What is this

Retinal vein occlusion → Lt is central (CRVO), Rt is branch (BRVO) → see hemorrhage and venous engorgement

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What is age related macular degeneration (AMD)

May present with metamorphosia = loss of straight line and scotoma = loss of central vision

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What is retinitis pigmentosa

Dystrophy of retina EP and photoreceptor → present as tunnel vision and nyctalopia = trouble seeing in dark

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<p>What is this </p>

What is this

Green = optic disc pallor

Purple = vss attenuation

Blue = pigmentation with spicule shaped margins

Are all TRIAD of findings for Retinitis pigmentosa

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What is leukocoria

Loss of red/orange reflection/glow → replaced with white/gray color found in congenital cataract and retinoblastoma

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What is papilledema

High ICP → bilateral optic disc edema → transient visual obscure/bigger blind spot

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What is ischemic optic neuropathy

AAION → caused by GCA and NAION

Lower flow to optic nerve head → altitudinal VFD

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How to pre chiasmatic from chiasmatic and post chiasmatic lesions

Pre chiasmatic respect HORIZONTAL meridian

Rest respect VERTICAL meridian

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Optic nerve lesion sign

Ipsilateral ANOPIA/blindness with positive RAPD/Marcus Gunn

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Bitemporal hemianopia is caused by lesion to what area

Optic chiasm → compression from mass (pituitary macroadenoma/craniopharyngioma etc)

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What is junctional scotoma

Distal optic nerve lesion and anterior chiasm → Wilbrand’s knee

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LGN stroke signs

Lateral posterior choroidal → incomplete, incongruous homonymous

(horizontal) sectoranopia

Anterior choroidal → incomplete quadruple sectoranopia OR incomplete homonymous hemianopia with horizontal sparing

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<p>based on this visual field where is the lesion</p>

based on this visual field where is the lesion

Lt → Lateral posterior choroidal of LGN

Rt → Anterior choroidal of LGN

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What is the difference between visual loss of Meyer and dorsal bundles

Meyers: In temporal lobe causes SUPERIOR quadrant loss from MCA infarct

Dorsal: In parietal lobe causes INFERIOR quadrant loss from PCA infarct

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Why is the macular area spared in infarction

Dual supply by PCA and MCA → if either infarct the remaining artery still supply

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What is monocular occipitotemporal crescent syndrome

Contralateral lesion of anterior occipital → controls the most PERIPHERAL part of field (60-90 degrees) → lesion causes loss of peripheral sight

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PNS control of pupil

Causes CONSTRICTION → neuron at EWN go to ciliary ganglion through CN III → synapse at short ciliary nerve of sphincter pupillary muscle → miosis

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Pathway of near pupillary reflex

Primary visual cortex → Supranuclear → Supraoculomotor area In midbrain → Oculomotor nucleus → MR → Convergence → EW nucleus → ciliary ganglion → Short ciliary n. Lens accommodation and miosis

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<p>What is this</p>

What is this

Argyll Robertson pupil → PRETECTAL defect → No light reflex + spare accommodation

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<p>What is this</p>

What is this

Adie’s tonic pupil → PSN ciliary ganglion damage → aberrant regeneration → poor light stimulus with better response to near object on affected eye

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SNS control of pupil

DILATION → from hypothalamus and synapse at C8-T2 ciliospinal center → travel across lung apex → superior cervical ganglion synapse → plexus ascend ICA → travel by opthalmic artery

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Horner syndrome triad

Miosis, anhidrosis, ptosis

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Cause of CN III palsy

EOM problem + headache = PComm Aneurism

DM, HT, atherosclerosis

EOM problem + pupil problem = compressive lesion

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What is MLF pathway

Frontal eye field → PPRF → abducen nucleus → LR movement → project to contralateral MLF → oculomotor nucleus → movement of MR

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What is INO

Lesion of MLF → show abducting eye nystagmus to stimulate CN III; MG can mimic this

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Cavernous sinus syndrome signs

  • Unilateral ophthalmoplegia (cranial nerve III, IV, VI)

- Autonomic dysfunction (Horner syndrome) or

- Sensory CN V1 - CN V2 loss

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Parts of the eye

Fibrous tunic: sclera and cornea

Vascular tunic/uvea: iris, ciliary body, choroid

Retina: pigmented and neural layer

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Parts of the uvea

Iris → muscles dilatory and sphincter

Ciliary body → zonule suspensory ligaments

Choroid → brown pigmented cells that absorb light