Week 2.03 Evaluation & Management Flashcards

1
Q

What are the pathways of neurogenic incomitancy

A

Supranuclear pathway - saccades, pursuits, vestibular
Internuclear pathways - gaze centres, ocular motor nuclei
Infranuclear pathways - ocular motor nerves

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2
Q

Which isolated palsies (on their own) are rare and usually congenital

A

Inferior rectus palsy

Superior rectus palsy

Fairly rare to have isolated palsies of any muscle which isn’t LR6 and SO4 as they are all associated with the same 3rd cranial nerve. Due to therefore be congenital

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3
Q

What are the main causes for acquired neurogenic palsies?

A

• Trauma
• Space-occupying lesions
o Tumour
o Vascular (aneurysm, carotid cavernous fluid)
• Vascular (microvascular: diabetes; hypertension vasculitis
• Inflammatory – e.g. tolosa-hunt syndrome, post viral (herpes zoster meningitis)
• Metabolic disorders

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4
Q

What is the most common neurogenic incomitancy

A

Most common neurogenic incomitancy is 6th nerve palsy (abducens) then 3rd nerve palsy (oculomotor) and then 4th nerve palsy (trochlear)

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5
Q

What is the aetiology of 6th nerve palsy

A

Birth trauma: instrumentation (forceps pressed against temporal bone)
Childhood: meningitis, pneumonia
Adult: diabetes, hypertension, trauma, demyelinating tissues
Old age: strokes

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6
Q

What’s the management for 6th nerve palsy

A
  • Prism base out to distance portion of bifocals - alleviate sxs of diplopia
  • An injection into opposing MR reduces esotropia to alleviate dip and prevents contracture of ipsilateral MR
  • Surgery
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7
Q

What is mobius syndrome

A
  • Congenital
  • 6th and 7th nerve palsy
  • loss of abduction and facial weakness
  • expressionless face, incomplete lid closure, bilateral loss of abduction
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8
Q

3rd nerve palsy aetiology

A
  • unilateral
  • aetiology: aneurysm, vascular disease - diabetes, hypertension, closed head injury
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9
Q

Complete oculomotor palsy

A
  • divergent strabismus
  • ptosis
  • mydriasis
  • loss of pupil action
  • accomodation
  • ‘down and out eye’
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10
Q

Incomplete or partial paresis

A
  • paresis of ciliary muscle and iris sphincter
  • can affect only superior or only inferior or single muscle palsy
  • double elevator palsy - px unable to raise eye cuz of palsy of SR and IO
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11
Q

Single muscle paresis

A
  • rare
  • congenital
  • SR with V pattern esotropia - check for ptosis to eliminate superior division palsy
  • MR very rare - check for Duane’s
  • IR not common - exclude mechanical restriction
  • IO very rare - diff diagnosis browns syndrome
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12
Q

If sudden onset of complete third nerve palsy with pupil involvement what do u do

A

Due to an intracranial aneurysm = neurosurgical emergency
If recent onset
Pain
Blown pupil
Go straight to CASUALTY

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13
Q

Management of third nerve palsy

A

Prisms - limited use diplopia only present if incomplete ptosis
Pilocarpine to reduce photophobia
Surgery?

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14
Q

What does Hess plot for 3rd nerve palsy look like

A

One eye the smaller inner square is massive
The other eye both squares are small and in and is down and out

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15
Q

4th nerve palsy (trochlear) - superior oblique

A
  • Least common neurogenic incomitancy
  • Common as both congenital and acquired
  • can be bilateral or unilateral
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16
Q

What can be the cause of 4th nerve palsy

A
  • familial defect
  • brain abnormality
  • many unknown
  • closed head injury - damage to the trochlea in upper cut blow in boxing
  • diabetes
  • intracranial tumour
17
Q

What are some mechanical incomitant deviations

A

Congenital:
Duanes retraction syndrome - problem with lateral rectus muscle
Browns syndrome - problem with SO
Mobius syndrome

Acquired:
Orbital injuries - fracture stopping the muscles
Dysthyroid eye disease

18
Q

Duanes retraction syndrome

A

Loss of movement of lateral rectus so can’t abduct
Psedotosis when looking away from underacting muscle

19
Q

What’s the cause of Duane’s retraction syndrome

A
  • Congenital structural abnormalities – fibrotic non elastic lateral rectus muscle
  • Paradoxical innervation – anomalous co-contraction of the medial and lateral rectus muscles
  • Innervational disturbance of brain stem origin
20
Q

What are some characteristics of Duane’s retraction syndrome

A

Bilateral or unilateral - more often affecting LE
Incidence higher in females
Incidence higher in females

21
Q

What does Duane’s retraction syndrome look like on Hess plot

A

Looks compressed
Don’t developed sequelae (mechanical) so hard to tell if recent or long standing

22
Q

Management of Duane’s syndrome

A
  • Treatment of amblyopia and correction of refractive error
  • Surgery for cosmetic correction of AHP, if necessary
23
Q

What’s browns syndrome

A

The problem when it goes through the trochlea. Failure to relax as it gets trapped in the trochlea. Muscle can do the job but when it relaxes gets trapped in the trochlea

24
Q

What can be the cause of browns syndrome

A
  • Superior oblique tendon sheath syndrome
  • Develops in infancy
  • mainly unilateral can be bilateral
    Short tension sheath, swelling on SO tendon
25
What does browns syndrome look like
Problem arises when the superior oblique has to relax so in the opposite direction V pattern Eye can’t supraduct May look like inferior oblique underaction
26
What does browns syndrome look like on Hess plot
Top bit of the bigger square on one eye is gone further down
27
Management of browns syndrome
• Most spontaneously recover • Some surgery for cosmetic correction of AHP
28
What is strabismus ficus
One or both eyes are fixed in position of extreme abduction Mechanical deviation
29
Compare neurogenic and mechanical deviations
Neurogenic head tilt is usual in vertical muscle palsies Mechanical head tilt is rare Neurogenic = ductions>versions Mechanical = ductions = versions Neurogenic = sequelae can fully develop over time Mechanical = do not develop
30
What are the main causes of myogenic palsy
Thyroid eye disease Myasthenia Rhabdomyosacoma
31
What are non paretic incomitancies
Alphabet patterns More convergent in downwards gaze than upwards