Eyes Flashcards
Pupils - definition and causes
Miosis
Mydriasis
Anisocoria
Miosis - constricted pupil - Horner’s syndrome, Pontine lesion, Drugs (opioids, anti-psychotics, anti-histamines, cholinergics)
Mydriasis - dilated pupil - Injury to CN 3, epilepsy, stroke, coning, iritis, drugs (anticholinergis, serotinergics, GABA)
Anisocoria - Uneven pupils - 20% physiological, Horners, uveitis, glaucoma, 3rd nerve palsy.
Pupils - definition and causes
Adies pupil
Parinaud pupil
Argyll Robertson
Adies pupil - Lesion in the efferent parasympathetic pathway (cilliary body) . Slowed reaction to light, intact accomodation.
Triad - Loss of reaction to light, decreased tendon reflexes (usually lower limb), hyperhydrosis.
Parinaud pupil (dorsal midbrain)- Loss of vertical upward gaze due to defect in the medial longitudinal fasciculus. Supranuclear therefore still has dolls head reflex. - convergence-retraction nystagmus = upward nystagmus and retracting globes. - pseudo-Argyll Robertson pupils - reduced accomodation. Causes - Central: pinealoma, multiple sclerosis, vascular lesions. Peripheral: trauma, diabetes mellitus, other vascular lesions, idiopathic, raised intracranial pressure
Argyll Robertson - Lesion in the midbrain - Dilated pupil - Does not react to light but reacts to accommodation - Neurosyphilis diabetic neuropathy, brain injury, thiamine deficiency, and mitral regurgitation.
Absent light reflex, intact accommodation
- Midbrain lesion (e.g. Argyll Robertson pupil)
- Ciliary ganglion lesion (e.g. Adie’s pupil)
- Parinaud’s syndrome
- Bilateral afferent pupil defects
Difference between optic tract and occipital lobe lesion
both cause a hemianopia - Occipital lobe is macular sparing
Causes of Papilledema
● Space-occupying lesion (causing raised intracranial pressure) or a retro-orbital mass
● Hydrocephalus (associated with large ventricles)
o Obstructive
o Communicating
▪ Increased formation of CSF – choroid plexus papilloma
▪ Decreased formation of CSF – tumour causing venous compression, subarachnoid space obstruction from meningitis
● Benign intracranial hypertension
o Idiopathic, contraceptive pill, Addison’s disease, nitrofurantoin/tetracycline/vitamin A/steroids
o Lateral sinus thrombosis
● Hypertension (grade IV)
● Central retinal vein thrombosis
● Cerebral venous sinus thrombosis
Causes of optic neuropathy
● Multiple sclerosis
● Toxic: ethambutol, chloroquine, nicotine, alcohol
● Metabolic: Vitamin B12 deficiency
● Ischaemia: diabetes mellitus, temporal arteritis, atheroma
● Familial – Leber’s disease
● Infective – infectious mononucleosis
Causes of ptosis
WITH NORMAL PUPILS ● Senile ptosis ● Myotonic dystrophy ● Fascioscapulohumeral dystrophy ● Ocular myopathy, e.g. mitochondrial myopathy ● Thyrotoxic myopathy ● Myasthenia gravis ● Botulism ● Fatigue ● Congenital WITH CONSTRICTED PUPILS ● Horner’s syndrome ● Tabes dorsalis WITH DILATED PUPILS ● Third nerve lesion
Causes of Nystagmus
● Horizontal:
o Vestibular lesion – chronic lesions cause nystagmus to the side of the lesion
o Cerebellar lesion – unilateral disease causes nystagmus to the side of the lesion
o Internuclear ophthalmoplegia – nystagmus is in the abducting eye, with failure of adduction on the AFFECTED SIDE. This is the result of a medial longitudinal fasciculus lesion. The most common cause in young adults with bilateral involvement is multiple sclerosis; in the elderly consider brainstem infarction
● Vertical:
o Brain stem lesion:
▪ Upbeat nystagmus suggests a lesion in the floor of the fourth ventricle
▪ Downbeat nystagmus suggests a foramen magnum lesion
o Toxic – phenytoin, alcohol (may also cause horizontal nystagmus)
Causes of unilateral blindness
retinal artery/vein occlusion, temporal arteritis, optic neuritis
Causes of bilateral blindness
Sudden: bilat occipital infarct, bilat optic nerve damage (methyl alcohol).
Gradual: glaucoma, cataracts, macular degeneration, vitreous hemorrhage, optic nerve compression.
Causes of decreased visual acuity
Corneal: scarring, Vitamin A deficiency
Lens: Refractive error, Cataracts
Retinal: macular degeneration, proliferative retinopathy, RP, retinal haemorrhage, retinal detachment
Neurovascular: Optic neuritis, retinal artery or vein occlusion, papilloedema
Glaucoma
Toxins - mercury/methanol
Amblyopia - Congenital disorder
What is Tolosa-Hunt Syndrome
Rare condition due to compressive changes in the orbit from inflammatory granuloma
Features - unilateral III, IV, V, VI palsies - severe headache - eye pain
Periorbital inflammatory changes found in MRI
Appearance and causes of optic atrophy
Pale, well demarcated disc on fundoscopy
usually bilateral, causing gradual loss of vision
Acquired - MS - longstanding papilloedema - raised intraocular pressure: glaucoma, tumour - retinal damage: choroiditis, retinitis pigmentosa - ischaemia - toxins: tobacco amblyopia, quinine, methanol, arsenic, lead - nutritional: B1, B2, B6, B12 deficiency
Congenital - Friedreich’s ataxia - mitochondrial disorders
Hypertensive eye changes
- Silver wiring
- AV nipping
- flame haemorrhages and soft (cotton wool) exudates, hard exudates.
- Papilloedema
Diabetic eye changes
NON-PROLIFERATIVE
● Haemorrhages:
o Dot haemorrhage into the inner retinal areas
o Blot-haemorrhage into more superficial nerve fibre areas
o Hard exudates have straight edges – leakage of protein and lipids from damaged capillaries
o Soft exudates (cotton wool spots) have a fluffy appearance owing to microinfarcts
o Microaneurysms
o Dilated veins
PROLIFERATIVE ● New vessels ● Vitreous haemorrhage ● Scar formation ● Retinal detachment ● Laser scars (small brown or yellow spots)