Ophthalmology #3 Flashcards

1
Q
What is the strongest risk factor for developing dry age-related macular degeneration out of the following: 
Hypertension
Poor diet
Smoking 
Diabetes Mellitus
Alcohol excess
A

Smoking

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2
Q

Which eye drops are used to confirm a Horner’s pupil?

What is the mechanism?

A

Apraclonidine eye drops

Apraclonidine stimulates alpha-1 and alpha-2 receptors. When added to the affected eye, it causes pupil dilation by >2mm because of relative supersensitivity of this pupil to alpha-1 receptor activity.

In a normal pupil, it causes constriction due to the more potent activity at the alpha-2 receptor which triggers reuptake of noradrenaline in the synaptic cleft.

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3
Q

After using Apraclonidine eye drops to confirm Horner’s pupil, what is Hydroxyamphetamine used for?

A

Hydroxyamphetamine is used to distinguish between first/second or third order neurones.

-> it will distinguish either a lesion in the brainstem, cervical cord, chest or next and one affecting above the superior cervical ganglion at the carotid bifurcation.

A normal pupil or a first/second order Horner’s pupil will dilate secondary to increased levels of noradrenaline released from the post-synaptic neurones.
In a third order neurone, this will not occur.

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4
Q

What is meant by a ‘first order neuron’ in relation to determining the cause of a Horner’s pupil?

A
Central (First Order Neuron) Horner's:
- Anhydrosis of the face, arm and trunk 
Includes:
- Stroke
- Syringomyelia
- Multiple Sclerosis
- Tumour 
- Encephalitis
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5
Q

What is meant by a ‘Second Order Neuron’ in relation to determining the cause of a Horner’s pupil?

A
Preganglionic (Second Order Neuron) Horner's:
- Anhydrosis of the face
Includes:
- Pancoast's Tumour
- Thyroidectomy
- Trauma
- Cervical rib
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6
Q

What is meant by ‘Third Order Neuron’ or ‘Postganglionic Lesion’ in relation to determining the cause of a Horner’s pupil? /

A
Third Order Neuron (Postganglionic) Lesion:
- No anhidrosis
Includes:
- Carotid artery dissection
- Carotid aneurysm
- Cavernous sinus thrombosis
- Cluster headache
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7
Q

If ‘heterochromia’ is a feature of Horner’s syndrome, what does this tell you?

A

Heterochromia (difference in iris colour) is seen in congenital Horner’s.

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8
Q

What are the 4 cardinal features of Horner’s syndrome?

A
  • Miosis (small pupil)
  • Ptosis
  • Anhidrosis (loss of sweating on one side)
  • Enophthalmos (sunken eye)
  • > in reality, the appearance is due to a narrow palpebral aperture rather than true enophthalmos
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9
Q

A patient has optic atrophy. What would you see on fundoscopy?

A

A pale, well demarcated disc.
Usually bilateral.
Causes a gradual loss of vision.

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10
Q

List some acquired causes of Optic Atrophy.

A
  • Multiple Sclerosis
  • Papilloedema (long standing)
  • Raised intraocular pressure (glaucoma, tumour)
  • Retinal damage (choroiditis, retinitis pigmentosa)
  • Ischaemia
  • Mitochondrial disorders (eg. Leber’s optic atrophy)
  • Wolfram’s Syndrome (aka DIDMOAD): the association of Diabetes Insipidus, Diabetes Mellitus, Optic Atrophy and Deafness
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11
Q

A 34yo female attends A&E. Confused over the last 3 days.
Longstanding history of psoriasis.
Basic obs are normal. CT head unremarkable.
Fundoscopy reveals bilateral papilloedema.
What is the likely cause?
- Encephalitis
- Brain abscess
- Primary brain tumour
- Vitamin A toxicity
- Hydrocephalus

A

Vitamin A toxicity

  • a rare cause of papilloedema
  • Pt is likely to have been taking retinoids for psoriasis.

Notes:

  • Encephalitis doesn’t usually present with papilloedema.
  • All other options are less likely as CT head is normal.
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12
Q

Describe ‘papilloedema’.

A

Optic disc swelling that is caused by increased intracranial pressure. It is almost always bilateral.

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13
Q

What features might you see on fundoscopy of a patient with papilloedema?

A
  • Venous engorgement
  • Loss of venous pulsation
  • Blurring of the optic disc margin
  • Elevation of optic disc
  • Loss of the optic cup
  • Paton’s lines: concentrical / radial retinal lines cascading from the optic disc.
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14
Q

List some causes of papillodema.

A
  • Space occupying lesion: neoplastic, vascular
  • Malignant hypertension
  • Idiopathic intracranial Hypertension
  • Hydrocephalus
  • Hypercapnia

Rare causes include:

  • Hypoparathyroidism
  • Hypocalcaemia
  • Vitamin A toxicity.
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15
Q

A 71yo man who has recently been diagnosed with macular degeneration asks for advice regarding antioxidant dietary supplements. Which of the following may contraindicate the prescription of such supplements?

  • Current smoker
  • Pernicious anaemia
  • Treated hypertension
  • History of depression
  • Previous episodes of tendonitis
A

Current smoker

  • Beta-carotene has been found to increase the risk of lung cancer and hence antioxidant dietary supplements are not recommended for smokers.
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16
Q

Dorzolamide eye drops are given to a 67yo male who is known to have raised intraocular pressure (glaucoma). What is the mechanism of action of this drug?

A

Carbonic Anhydrase inhibitor.

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17
Q

How might a patient with Optic Neuritis present?

A

Typically a unilateral decrease in visual acuity over hours or days. There may be poor discrimination of colours and eye pain on movement.

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18
Q

Which one of the following is associated with the Holmes-Adie pupil?

  • Decreased ankle reflexes
  • Pupillary constriction
  • Ptosis in 10 - 20% of cases
  • Increased risk of developing MS
  • Neurosyphilis
A

Decreased ankle reflexes

Holmes-Adie syndrome:
Association of Holmes-Adie pupil with absent ankle/knee reflexes.

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19
Q

What is a ‘Holmes-Adie’ pupil?

A

A benign condition most commonly seen in women. It is one of the differentials of a dilated pupil.

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20
Q

Give an overview of a ‘Holmes-Adie’ pupil.

A
  • Unilateral in 80% of cases
  • Dilated pupil
  • Once the pupil has constricted, it remains small for an abnormally long time
  • Slowly reactive to accommodation but very poorly (if at all) to light.
21
Q

Which one of the following is the most common ocular manifestation of Rheumatoid Arthritis?

  • Scleritis
  • Episcleritis
  • Keratoconjunctivitis sicca
  • Corneal ulceration
  • Keratitis
A

Keratoconjunctivitis sicca

-> a dry, burning, gritty eyes caused by decreased tear production.

22
Q

Each of the following cause a mydriatic pupil except:

  • Third nerve palsy
  • Atropine
  • Holmes-Adie pupil
  • Argyll-Robertson pupil
  • Traumatic iridoplegia
A

Argyll-Robertson pupil

  • Sometimes seen in Neurosyphilis
  • Accommodates but doesn’t react.
23
Q

Describe the features of an Argyll-Robertson pupil

A
  • Small, irregular pupils

- No response to light, but there is a response to accommodate

24
Q

What are the causes of an Argyll-Robertson pupil?

A
  • Diabetes Mellitus

- Syphilis

25
Q

List 5 causes of mydriasis (large pupil).

A
  • Third nerve palsy
  • Holmes-Adie pupil
  • Traumatic iridoplegia
  • Phaeochromocytoma
  • Congenital
  • Anisocoria (different sized pupils) may result in apparent mydriasis, due to the difference with the other pupil
26
Q

List some drug causes of mydriasis (large pupil).

A
  • Topical mydriatics: Tropicamide, Atropine
  • Sympathomimetic drugs: Amphetamines, Cocaine
  • Anticholinergic drugs: Tricyclic Antidepressants
27
Q

Which of the following conditions is associated with Retinitis Pigmentosa?

  • ADPKD
  • Tuberous sclerosis
  • Von Hippel-Lindau syndrome
  • Alport’s syndrome
  • Medullary sponge kidney
A

Alport’s Syndrome is associated with Retinitis Pigmentosa.

28
Q

Describe the visual loss associated with Retinitis Pigmentosa

A
  • Primarily affects the peripheral retina, resulting in tunnel vision
  • Night blindness is often the initial sign
  • Fundoscopy: black bone spicule-shaped pigmentation in the peripheral retina, mottling of the retinal pigment epithelium.
29
Q

Which diseases are associated with Retinitis Pigmentosa?

A
  • Refsum disease: cerebellar ataxia, peripheral neuropathy, deafness, ichthyosis
  • Usher syndrome
  • A-beta-lipoproteinemia
  • Lawrence-Mood-Biedl syndrome
  • Kearns-Sayre syndrome
  • Alport’s syndrome
30
Q

A 65yo man with a known history of Paget’s disease is noted to have dark red lines radiating from the optic nerve. What is the likely diagnosis?

  • Retinitis pigmentosa
  • Optic neuritis
  • Angioid retinal streaks
  • Choroidoretinitis
  • Malignant hypertension
A

Angioid retinal streaks

31
Q

What are ‘Angioid retinal streaks’?

A

Angioid retinal streaks are seen on fundoscopy as irregular dark red streaks radiating from the optic nerve head.

32
Q

What are ‘Angioid retinal streaks’ caused by?

A

Caused by degeneration, calcification and breaks in Bruch’s membrane.

33
Q

What are the causes of Angioid retinal streaks?

A
  • Pseudoxanthoma elasticum
  • Ehler-Danlos syndrome
  • Paget’s disease
  • Sickle cell Anaemia
  • Acromegaly
34
Q

Which of the following causes of Horner’s syndrome is due to a central lesion?

  • Cavernous sinus thrombosis
  • Internal carotid aneurysm
  • Syringomyelia
  • Pancoast’s tumour
  • Cervical rib
A

Syringomyelia

35
Q

Explain how you would distinguish between a central, pre-ganglionic, and post-ganglionic cause of Horner’s syndrome.

A

Anhydrosis determines site of lesion:
- Head, arm, trunk = central lesion: eg. stroke, syringomyelia

  • Just face = pre-ganglionic lesion: eg. Pancoast’s tumour, cervical rib
  • Absent = post-ganglionic: eg. carotid artery
36
Q

80yo woman with flashes and floaters in the visual field of her right eye. Likely diagnosis?

A

Posterior vitreous detachment

37
Q

Describe the epidemiology of posterior vitreous detachment.

A
  • Posterior Vitreous detachment is thought to occur in up to 50 - 75% of the population over 65 years old.
    Such patients are usually reviewed by an Ophthalmologist to assess the risk of progressing to retinal detachment.
38
Q

What is the mechanism of action of Latanoprost in the management of Primary Open-Angle Glaucoma?

A

Increases uveoscleral outflow.

Latanoprost is a prostaglandin analogue used in glaucoma.

39
Q

A 55yo male presents to A&E with Giant Cell Arteritis. Which of the following structural deficits has lead to the relative afferent pupillary defect?

  • Ischaemic optic neuropathy
  • Blindness
  • Optic Neuritis
  • Photophobia
  • Corneal opacity
A

Ischaemic Optic Neuropathy occurs in Giant Cell Arteritis (GCA) as a result of an inflammatory process of the blood vessels in the head.

This optic nerve lesion may manifest in a relative afferent pupillary defect (RAPD) aka Marcus-Gunn pupil.

40
Q

Which test would you use to identify a Marcus-Gunn pupil?

What causes as Marcus-Gunn pupil?

A
  • Swinging Light test
  • Marcus-Gunn (Relative Afferent Pupillary Defect) pupil is caused by a lesion anterior to the optic chiasm (i.e. optic nerve or retina)
41
Q

What would be your findings on the swinging light test if you had a patient with a Marcus-Gunn pupil?

A
  • Affected and normal eye appears to dilate when light is shone on the affected eye.
42
Q

What are the causes of a Marcus-Gunn pupil?

A
  • Retina: detachment

- Optic nerve: optic neuritis eg. Multiple Sclerosis

43
Q

Describe the pathway of pupillary light reflex (both afferent and efferent).

A

Afferent: Retina -> Optic Nerve -> Lateral Geniculate Body -> Midbrain

Efferent: Edinger-Westphal nucleus (midbrain) -> Oculomotor nerve

44
Q
49yo male presents with acute onset loss of vision in the right eye preceded by a 2-hour history of progressively enlarging dark spots in his vision. 
He has Type 1 diabetes mellitus (diagnosed 15 years ago) which is poorly controlled. 
What is the most likely diagnosis? 
- Ocular migraine
- Retinal detachment 
- Vitreous haemorrhage
- Ischamic optic neuropathy
- Retinal artery occlusion
A

Vitreous haemorrhage

Vitreous haemorrhage is a cause of sudden painless loss of vision in the context of diabetic retinopathy.

It usually presents with dark spots (scotoma) in the vision initially. This man is likely to have diabetic retinopathy.

45
Q

Give some differentiating features of posterior vitreous detachment.

A
  • Flashes of light (photopsia) in the peripheral field of vision
  • Floaters, often on the temporal side of the central vision.
46
Q

Give some differentiating features of retinal detachment.

A
  • Dense shadow that starts peripherally and progresses towards the central vision
  • A veil / curtain over the field of vision
  • Straight lines appear curved
  • Central visual loss
47
Q

Give some differentiating features of Vitreous Haemorrhage.

A
  • Large bleeds cause sudden visual loss
  • Moderate bleeds may be described as numerous dark spots
  • Small bleeds may cause floaters.
48
Q

Which one of the following causes of Horner’s syndrome is due to a lesion in the post-ganglionic part of the nerve supply?

  • Internal carotid aneurysm
  • Stroke
  • Syringomyelia
  • Pancoast’s tumour
  • Thyroidectomy
A

Internal carotid aneurysm

-> there will be no anhydrosis

49
Q

A 15yo boy presents to the GP with some skin changes of the neck. These started as a small area, but have now got a lot bigger and more obvious.
On examination, there is a large areas of small, yellow papules 1-5mm in diameter in a reticular patter and coalescing at places into plaques. The skin has a ‘plucked chicken’ appearance. The boy reports no problem with his vision.
What would you be likely to find on fundoscopy?
- Angioid retinal streaks
- Lisch nodules
- Cotton wool spots
- Neovascularisation
- Bone spicules

A

Angioid retinal streaks

Angioid streaks are small breaks in Bruch’s membrane, an elastic tissue containing membrane of the retina.
It is a feature of pseudoxanthoma elasticum.
The earliest sign in pseudoxanthoma elasticum is skin changes.