ENT: Facial palsy Flashcards

1
Q

what is Facial nerve palsy?

A

isolated dysfunction of the facial nerve

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2
Q

how does Facial nerve palsy present?

A

unilateral facial weakness

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3
Q

where does the facial nerve emerge from and which structures does it pass through?

A

brainstem at the cerebellopontine angle

it passes through the temporal bone and parotid gland.

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4
Q

the facial nerve divides into which 5 branches?

A
Temporal
Zygomatic
Buccal
Marginal mandibular
Cervical
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5
Q

what is the function of the facial nerve?

A

Motor: Supplies the muscles of facial expression, the stapedius in the inner ear and the posterior digastric, stylohyoid and platysma muscles in the neck.

Sensory: carries taste from the anterior 2/3 of the tongue.

Parasympathetic: it provides the parasympathetic supply to the submandibular and sublingual salivary glands and the lacrimal gland (stimulating tear production).

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6
Q

with reference to Facial nerve palsy, how would an upper motor neurone lesion present?

A

the forehead will be spared and the patient can move their forehead on the affected side.

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7
Q

with reference to Facial nerve palsy, how would a lower motor neurone lesion present?

A

the forehead will NOT be spared and the patient cannot move their forehead on the affected side.

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8
Q

which cranial nerve is the facial nerve?

A

CNVII (7)

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9
Q

what are the three types of nerve injury?

A

Neuropraxia
Axonotmesis
Neurotmesis

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10
Q

what is Neuropraxia?

A

nerve injury:

  • mildest form
  • due to pressure on the nerve (being squashed)
  • conduction block of function without nerve degeneration
  • reversible if pressure taken away
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11
Q

what is Axonotmesis?

A

nerve injury:

  • more severe Neuropraxia
  • The axons and their myelin sheath are damaged
  • due to pressure on the nerve (being squashed)
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12
Q

what is Neurotmesis?

A

nerve injury:

  • total nerve transection
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13
Q

what investigations would you do to diagnose Facial nerve palsy?

A

Audiometry
Stapedius reflexes
MRI / CT
ENG/EMG (neurophysiology)

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14
Q

how do you manage Bell’s Palsy?

A

If patients present within 72 hours of developing symptoms - prednisolone

  • lubricating eye drops
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15
Q

what is Bell’s palsy?

A

Bell’s palsy is an acute unilateral peripheral facial nerve palsy in patients for whom physical examination and history are otherwise unremarkable, consisting of deficits affecting all facial zones equally that fully evolve within 72 hours.

NB: facial palsy that is progressive, waxing and waning, or affects facial zones in an uneven fashion, is not Bell’s palsy.

  • single episode
  • unilateral
  • absence of other symptoms
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16
Q

the herpes zoster virus can cause which time of facial nerve palsy?

A

Ramsay-Hunt Syndrome

17
Q

which virus causes Ramsay-Hunt Syndrome?

A

herpes zoster virus

18
Q

how does Ramsay-Hunt Syndrome present?

A
  • unilateral lower motor neurone facial nerve palsy

- painful/tender vesicular rash in ear canal

19
Q

how do you manageRamsay-Hunt Syndrome?

A

Treatment should ideally be initiated within 72 hours. Treatment is with:

Prednisolone
Aciclovir

Patients also require lubricating eye drops.

20
Q

what is Myasthenia gravis?

A

autoimmune condition that causes muscle weakness that gets progressively worse with activity and improves with rest

Circulating antibodies against the nicotinic acetylcholine receptor (AChR) and associated proteins impair neuromuscular transmission.

21
Q

what type of people does Myasthenia gravis typically affect?

A

Interestingly myasthenia gravis affects men and women at different ages. Typical patients are either a woman under the age of 40 or a man over the age of 60.

  • people tumours of thymus gland
22
Q

when are the symptoms of Myasthenia gravis typically worse?

A

Symptoms are typically minimal in the morning and worst at the end of the day.

23
Q

how might Myasthenia gravis present?

A

The symptoms most affect the proximal muscles and small muscles of the head and neck. It leads to:

  • Extraocular muscle weakness causing double vision (diplopia)
  • Eyelid weakness causing drooping of the eyelids (ptosis)
  • Weakness in facial movements
  • Difficulty with swallowing
  • Fatigue in the jaw when chewing
  • Slurred speech
  • Progressive weakness with repetitive movements
24
Q

what investigations would you do to diagnose Myasthenia gravis?

A

Diagnosis can be made testing directly for the relevant antibodies:

Acetylcholine receptor (ACh-R) antibodies (85% of patients)

Muscle-specific kinase (MuSK) antibodies (10% of patients)

LRP4 (low-density lipoprotein receptor-related protein 4) antibodies (less than 5%)

A CT or MRI of the thymus gland is used to look for a thymoma.

25
Q

what are the treatment options for Myasthenia gravis?

A
  1. Reversible acetylcholinesterase inhibitors (usually pyridostigmine or neostigmine) increases the amount of acetylcholine in the neuromuscular junction.
  2. immunosuppression (e.g. prednisolone or azathioprine).
  3. thymectomy.
26
Q

what is Myasthenic Crisis?

A

Myasthenic crisis is a severe complication of myasthenia gravis. It can be life threatening. It causes an acute worsening of symptoms, often triggered by another illness such as a respiratory tract infection.