Horner's Syndrome Flashcards

1
Q

What is horner’s syndrome?

A

A condition that results from the disruption of the sympathetic nerves supplying the face resulting in a triad of:

  • Ptosis
  • Miosis
  • Anhydrosis
  • (and enophthalmos)
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2
Q

Summarise the pathophysiology of Horner’s syndrome

A

Damage to the oculosympathetic pathway, at the level of either:

  • 1st order neurones
  • 2nd order neurones
  • 3rd order neurones
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3
Q

Describe the pathways of 1st - 3rd order neurones.

A

Damage to the oculosympathetic pathway, at the level of either:

  • 1st order neurones
    • hypothalamus –> synapes in spinal cord level T1
  • 2nd order neurones
    • spinal cord level T1 –> synapses in superior sympathetic ganglion of sympathetic chain
  • 3rd order neurones
    • superior sympathetic ganglion of sympathetic chain –> travels along nerves that follow path of common carotid artery –> forms internal carotid plexus –> synapes at NMJ of:
      • pupillary dilator muscles
      • Muller’s muscle
      • sweat glands
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4
Q

What are some CENTRAL causes of Horner’s syndrome?

A

Causes can be divided according to presence & location of anhidrosis:

Central involving hypothalamospinal tract (anhidrosis of face, arm and trunk) - 1st order neurones

  • Strokes
  • tumours
  • MS
  • encephalitis
  • lateral medullary syndrome
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5
Q

What are some PRE-GANGLIONIC causes of Horner’s syndrome?

A

Preganglionic (anhidrosis of face) - 2nd order neurones

  • Pancoast tumor i.e. bronchogenic carcinoma on lung apex
  • Thyroid carcinoma
  • Thyroidectomy
  • Goiter
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6
Q

What are some POST-GANGLIONIC causes of Horner’s syndrome?

A

Postganglionic (no anhidrosis) - 3rd order neurones

  • Carotid artery dissection/carotid artery aneurysm
  • Cluster headache
  • Migraine –> episode of Horner’s –> relieved post-migraine
  • Cavernous sinus thrombosis
  • Otitis media
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7
Q

What are the presenting symptoms of Horner’s syndrome?

A
  • Inability to open the eye fully on the affected side
  • Loss of sweating on affected side
  • Facial flushing
  • Orbital pain/headache
  • Other symptoms based on CAUSE
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8
Q

What are the signs of Horner’s syndrome O/E?

A

SPAM

  • sympathetic fibres
  • ptosis
  • anhydrosis
  • miosis

ipsilateral to side of sympathetic nerve damage

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9
Q

What are the primary investigations for ?Horner’s syndrome?

A
  • Cocaine drop test
    • positive result = no dilation of pupil
  • Apraclonidine test
    • positive result = dilation of pupil
  • Paredrine test
    • helps to ascertain if lesion is on 3rd order neurone
    • ​3rd order neurone affected = no dilation of pupil
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10
Q

How does the cocaine drop test work?

A

Normal eye:

  • Cocaine eyedrops block reuptake of post- ganglionic norepinephrine
  • –> retention of norepinephrine in the synapse
  • –> dilation of a normal pupil

BUT, in Horner’s syndrome:

  • the lack of norepinephrine in the synaptic cleft
  • –> mydriatic failure i.e. lack of dilation
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11
Q

What is paredrine?

A
  • major metabolite of amphetamine
  • drug that stimulates sympathetic nervous system
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12
Q

How does the paredrine test work?

A

If the 3rd order neuron (discharges norepinephrine into the synaptic cleft) is intact:

  • amphetamine –> neurotransmitter vesicle release –> releases norepinephrine into synaptic cleft –> mydriasis of affected pupil.

If lesion is of the 3rd order neuron:

  • amphetamine has no effect –> pupil remains constricted
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13
Q

How does the apraclonidine test work?

A

weaker form of norepinephrine

In Horner’s syndrome, the sympathetic innervation to pupillary dilator muscle is lost

  • —> affected pupil = miotic
  • –> pupillary dilator muscle responds to denervation by increasing α1 receptors

Apraclonidine is useful in this case due to:

  • its weak α1-adrenergic properties.
  • When applied to denervated (hyper-sensitive) pupillary dilator
  • a super-normal dilatory response is generated
  • –> pupil dilates to a more than it would it in a a non-denervated muscle
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14
Q

What are some secondary investigations that are conducted once a diagnosis of Horner’s syndrome is reached?

A

To find CAUSE of Horner’s syndrome:

  • CXR - apical lung tumour
  • CT/MRI - cerebrovascular accidents
  • CT angiography - carotid artery dissection
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15
Q

How is Horner’s syndrome managed?

A

Horner’s syndrome is a sign not a disease in itself

  • So, management depends on CAUSE
  • (e.g. management for carotid dissection is very different to management of Pancoast’s tumours)
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16
Q
  1. What are some complications of Horner’s syndrome?
  2. What is the prognosis of Horner’s syndrome?
A
  1. depends on CAUSE
  2. depends on CAUSE