CNIII Palsy Flashcards

1
Q

Where does the CNIII originate from?

A

Oculomotor Nucleus at the midbrain of the brainstem and emerges from the anterior aspect of the midbrain

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2
Q

How does CNIII pass after leaving the anterior aspect of the midbrain?

A

Then passes inferiorly to the posterior cerebral artery and superiorly to the superior cerebellar artery. It pierces the dura mater and then enters the lateral aspect of the cavernous sinus.

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3
Q

What is the course of CNIII from the cavernous sinus?

A

In the cavernous sinus it receives sympathetic branches from the internal carotid plexus that travel within the sheath of the oculomotor nerve. It leaves via the superior orbital fissure and divides into superior and inferior branches.

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4
Q

What is involved in the superior branch of CNIII?

A

Superior – superior rectus and LPS. Sympathetic fibres run with this to innervate the superior tarsal muscle

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5
Q

What fibres run with the superior branch of CNIII and what do they innervate?

A

Sympathetic fibres run with this to innervate the superior tarsal muscle

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6
Q

What is included in the inferior branch of CNIII?

A

Inferior – Inferior rectus, medial rectus and inferior oblique. Supplies pre-ganglionic parasympathetic fibres to the ciliary ganglion that innervates the sphincter pupillae and ciliary muscles.

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7
Q

What are the common aetiologies of CNIII palsy?

A
  • Raised IOP that compressed the nerve against the temporal bone
  • Posterior communicating artery aneurysm
  • Cavernous sinus infection or trauma
  • Diabetes, MS, myasthenia gravis and giant cell arteritis
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8
Q

In what type of CNIII palsy are the majority of cases idiopathic?

A

Congenital CNIII palsies

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9
Q

What is the aetiology of congenital CNIII palsy?

A

There is some evidence of a familial tendency to the condition, particularly to a partial palsy involving the superior division of the nerve with an autosomal recessive inheritance. The condition can also result from aplasia or hypoplasia of one or more of the muscles supplied by the oculomotor nerve. It can also occur as a consequence of severe birth trauma.

Isolated idiopathic, hereditary (autosomal recessive), neurological defect (involves other signs and symptoms)

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10
Q

What are the common aetiologies of acquired CNIII palsies?

A
  • Vascular disorders such as diabetes, heart disease, atherosclerosis and aneurysm, particularly of the posterior communicating artery
  • Space occupying lesions or tumours, both malignant and non-malignant
  • Inflammation and infection
  • Trauma
  • Demyelinating disease (multiple sclerosis)
  • Autoimmune disorders such as myasthenia gravis
  • Post-operatively as a complication of neurosurgery
  • Cavernous sinus thrombosis
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11
Q

What motor actions does the CNIII do?

A

Motor –
Innervates the majority of the extraocular muscles (levator palpebrae superioris, superior rectus, inferior rectus, medial rectus and inferior oblique).

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12
Q

What parasympathetic/autonomic actions does CNIII do?

A

Parasympathetic/Autonomic – Supplies the sphincter pupillae and the ciliary muscles of the eye.

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13
Q

What sympathetic actions does CNIII do?

A

No direct function, but sympathetic fibres run with the oculomotor nerve to innervate the superior tarsal muscle (helps to raise the eyelid).

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14
Q

What are symptoms of CNIII palsy?

A
  • Ptosis (drooping upper eyelid) – unopposed activity of the orbicularis oculi muscle as result of LPS paralysis
  • ‘Down & Out’ eye position – paralysis of superior, inferior and medial rectus and the inferior oblique = unopposed activity of the lateral rectus and superior oblique
  • Mydriasis – unopposed action of the dilator pupillae muscle

If due to a compression by a PCA (posterior communicating artery aneurysm) it’ll be painful and mydriasis will be present. Trauma also involves the pupil.

Vascular acquired 3rd nerve palsy usually results in a full recovery

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15
Q

Which type of nerve palsy usually results in a full recovery?

A

Vascular acquired CNIII palsy

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16
Q

What AHP is expected in CNIII palsy? What symptoms will they experience with an AHP?

A
  • Head turn in the opposite direction to the affected eye
  • Notice AHP: in those with a single muscle affected/palsy, as only one is affected they should have a larger area of BSV.
    Those with a complete 3rd nerve palsy will have a small area of BSV due to a large area of incomitancy as a result of the affected EOMs and restricted ocular motility = likely to have an AHP
  • No AHP: anyone with complete 3rd nerve palsy, pupil involvement and ptosis.
    Because of the droopiness of the eyelid, it will obscure the diplopia and the px will see single
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17
Q

If there is no AHP in CNIII what does this mean?

A
  • No AHP: anyone with complete 3rd nerve palsy, pupil involvement and ptosis.
    Because of the droopiness of the eyelid, it will obscure the diplopia and the px will see single so don’t need an AHP
18
Q

What will CT show of CNIII palsies?

A
  • Incomitant exotropia (greater on head turn to the same side)
  • Hypotropia
  • Intorsion
  • Can be broken down between complete and incomplete 3rd nerve palsy
19
Q

How does a COMPLETE CNIII palsy look?

A

Ptosis and deviation will be out and down. Eye cannot move in, up or down. The pupil will be large and will not react to light.

20
Q

What will ones OMs look like in a COMPLETE CNIII palsy vs. an INCOMPLETE CNIII palsy?

A

Full – abduction

Limited – Elevation, depression, adduction

21
Q

How can COMPLETE CNIII palsy be classified?

A
  1. Both the superior and inferior divisions are involved
  2. Pupil may or may not be involved
  3. Total or partial (depending on severity of motility)
22
Q

What happens in complete CNIII when there’s a complete ptosis?

A

Outcome of complete ptosis in a congenital 3rd nerve palsy leads to stimulus deprivation amblyopia and suppression. It prevents diplopia but, as recovery occurs the lid improves and diplopia will be appreciated again.

When it is partial ptosis they may have some binocular potential with AHP and will result in strabismic amblyopia if the eyelid obstructs the pupil.

23
Q

What should we assume an acquired CNIII palsy is caused by until proven otherwise?

A

An acquired complete 3rd nerve palsy is presumed to be a result of posterior communicating artery aneurysm in absence of trauma until proven otherwise.

24
Q

What is Incomplete/Partial CNIII palsy divided into?

A

2 Divisional Palsies
- Superior Division (SR, LPS)
- Inferior Division (MR, IO, IR and inferior branch to ciliary ganglion controlling sphincter and ciliary muscle)

& Single Muscle Palsy (IR, SR, MR)

25
Q

What is Superior Division palsy?

A

A divisional partial/incomplete CNIII palsy of SR or LPS.
Usually a result of superior orbital fissure aetiology through trauma or tumours

26
Q

What is Inferior Division palsy?

A

A divisional partial/incomplete CNIII palsy of MR, IO, IR and inferior branch to ciliary ganglion controlling sphincter and ciliary muscle

27
Q

What is Single Muscle palsy?

A

An incomplete CNIII palsy of the IR, SR or MR
= will be diagnosed as Duanes Retraction Syndrome, Thyroid Eye Disease or Browns Syndrome

28
Q

What does a single muscle palsy of the IR need to be differentiated with?

A

A singular incomplete muscle palsy of the IR needs to be differentiated with Myasthenia Gravis (IR very rare, must exclude mechanical restrictions like thyroid eye disease)

29
Q

Are complete or incomplete CNIII palsies the most common?

A

Incomplete
Partial 3rd nerve palsies are more common than complete palsies and can present with variable duction limitations of the affected extraocular muscles and varying degrees of eyelid ptosis and/or pupillary dysfunction.

30
Q

What aetiologies for CNIII palsies can lead to pupil sparing?

A

Pupil sparing can occur in ischaemia as well as inflammatory and aneurysm. It is spared in diabetes and hypertension as it’s an occlusive disease of network of small blood vessels supplying the nerve (compressed or compromised). Pupillomotor fibres travel in outer layers of nerve therefore closer to nutrient blood supply enveloping the nerve therefore pupil responses are normal.

31
Q

What are the symptoms of complete CNIII palsy?

A

Complete 3rd nerve palsies will present with a complete eyelid ptosis with the eye in a downward and outward position and the inability to adduct, infraduct, or supraduct. Patients will also have a dilated pupil with sluggish reaction to light.

32
Q

What is Aberrant Regeneration?

A

Aberrant regeneration of the third cranial nerve, or oculomotor synkinesis, refers to the abnormal response to firing of the oculomotor nerve causing paradoxical co-contraction of muscles. Following an acute onset CNP a certain amount “miswiring” can occur as the damaged nerve regenerates, resulting in bizarre eye movements which do not improve with time or can be corrected with surgery.

The axons retract when damaged and grow forward again they enter wrong myelin tube to supply inappropriate muscles
IR to LPS

33
Q

What is aberrant regeneration common in?

A

CNIII palsy when caused by aneurysms, trauma, tumour (rare) and congenital (uncommon).

34
Q

In what cases of CNIII palsy is aberrant regeneration not going to occur?

A

It will not occur in diabetic or hypertensive cases which is presumed to be due to the structural framework of the nerve remaining intact.

35
Q

When is aberrant regeneration likely to occur?

A

This occurs around 5 weeks after the 3rd nerve palsy in children and 2-3 months after acute onset in adults.

36
Q

What are examples of aberrant regeneration?

A
  • Eyelid retraction / pupil constriction on adduction, upgaze and downgaze
  • Paradoxical eye movements (i.e. adduction on attempted up / downgaze)
37
Q

What are 4 features of aberrant regeneration?

A
  • Elevation of the upper eyelid on down-gaze or adduction (Pseudo Von-Graefe phenomenon)
  • Adduction of the eye on attempted up-gaze (the eye does not move entirely up, but adducts as well)
  • Pupil constriction on attempted adduction +/- down-gaze
  • Retraction of globe on attempted elevation / depression
    Co-contraction of SR / IR
38
Q

How do we check that CNIV palsy is not at play in a CNIII palsy?

A

Need to check that the 4th nerve is intact:
- Main action SO depression on ADDuction

  • Make patient abduct the eye and then try to look down as much as they can (even though px with 3rd nerve palsy won’t be able to depress a lot). Examiner should look for intorsion (iris landmark or conjunctival vessel) to confirm fourth nerve is intact

This is done because:
- Depression and adduction affected in 3rd nerve need to establish if 4th nerve functioning

  • Establish aetiology and therefore what scan to perform
39
Q

What are the ocular movement findings in CNIII?

A
  • Lift the ptotic lid except when looking for aberrant regeneration
  • Limitation of movement in all directions of gaze bar laterally and down in adduction
  • Limited adduction, elevation and depression. Unlikely to find a position of BSV due to degree of incomitance on ocular motility because the field of BSV will be extremely small (that’s why prisms aren’t beneficial for these patients)
40
Q

What is the field of BSV like in CNIII palsy?

A

Very small!
Unlikely to find a position of BSV due to degree of incomitance on ocular motility because the field of BSV will be extremely small (that’s why prisms aren’t beneficial for these patients) usually to the LR (abduction).

41
Q

Look at the Hess Charts!

A