Lesions affecting brainstem function Flashcards

1
Q

what are the parts of the brainstem

A

medulla oblongata

pons

pituitary gland

thalamus

(most pirates parrots talk)

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2
Q

where are the cranial nerves situated

A

cranial nerves are in the brainstem which is the part that enters the brain after the spinal cord

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3
Q

what are the cranial nerves

A

olfactory
optic
oculomotor
trochlear
trigeminal
abducens
facial
vestibular
glossopharnageal
vagus
accessory
hypoglossal

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4
Q

where do the cranial nerves lieT

A

The4 cranial nerves in the medullaareCN 9-12:
Glossopharyngeal (CN9): ipsilateral loss of pharyngeal sensation
Vagus (CN10): ipsilateral palatal weakness
Spinal accessory (CN11): ipsilateral weakness of the trapezius and stemocleidomastoid muscles
Hypoglossal (CN12): ipsilateral weakness of the tongueThe 12th cranial nerve is the motor nerve in the midline of the medulla. Although the 9th, 10th and 11th cranial nerves have motor components, they do not divide evenly into 12 (using our rule) and are thus not the medial motor nerves.
The4 cranial nerves in the ponsareCN 5-8:
Trigeminal (CN5): ipsilateral alteration of pain, temperature and light touch on the face back as far as the anterior two-thirds of the scalp and sparing the angle of the jaw.
Abducent (CN6): ipsilateral weakness of abduction (lateral movement) of the eye (lateral rectus).
Facial (CN7): ipsilateral facial weakness.
Auditory (CN8): ipsilateral deafness.The 6th cranial nerve is the motor nerve in the medial pons. The 7th is a motor nerve but it also carries pathways of taste, and using the rule of 4 it does not divide equally in to 12 and thus it is not a motor nerve that is in the midline. The vestibular portion of the 8th nerve is not included in order to keep the concept simple and to avoid confusion. Nausea and vomiting and vertigo are often more common with involvement of the vestibular connections in the lateral medulla.
The4 cranial nerves above the ponsareCN 1-4:
Olfactory (CN1): not in midbrain.
Optic (CN2): not in midbrain.
Oculomotor (CN3): impaired adduction, supradduction and infradduction of the ipsilateral eye with or without a dilated pupil. The eye is turned out and slightly down.
Trochlear (CN4): eye unable to look down when the eye is looking in towards the nose (superior oblique).The 3rd and 4th cranial nerves are the motor nerves in the midbrain.

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5
Q

what is the pyramidal tract

A

carries information from the brain to the muscle

fibres originate in the cerebral cortex carrying upper motor nerves fibres to the spinal cord
(corticospinal) and brainstem (corticiobulbar)

transmits signals for the voluntary control of the musculature of the body and the face

no synapses within descending pathways

upper motor neurone from brain then lower motor neurone to the muscle

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6
Q

where do fibres pass in the pyramidal tract

A

fibres pass from the cereal cortex to the brainstem and the spinal cords

they synapse to the lower motor neurones

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7
Q

what are cerebral penducels

A

two stalks which attaches the cererbrum to the brainstalk (largest portion of the brain the pink cloudy bit

located on the anterior part of the midbrain

contains the easending and descending nerve fibres between the brain and the brainstem

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8
Q

what is the red nucleus

A

lies within the midbrain

the red nucleus is pale pink due to the presence of iron

recievies inputs from the cerebellum of the opposite side

and the motor cortex of the same side

function = coordinate motor movement

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9
Q

what are the three types of brainstem lesions

A

three categories

nucelar

internuclear

infra nuclear - below the level of the nuclei

generally nuclear palsies are a rare occurrence

and often associated with other neurological signs because of other structures in close proximity

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10
Q

what is the difference between nuclear , internuclear and infranuclear lesions

A

nuclear - lesion at the level of the nucleus

internuclear pathway - between two nuclei - i.e. the third and 6th -

infra nuclear - affects nerve not brain - e.g. hypertensive/ diabetic

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11
Q

describe the contents of the oculomotor nerve

A

2 nuclei

oculomotor nerve nucleus - superior rectus , inferior rectus , and levator palpabrae superioris

2 types of efferent nerve fibres - somatic innervate the (eoms) and visceral innervate the (sphincter and cillary body) - parasympathetic

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12
Q

where does the third nerve enter and exit the skull

A

originates at the level of the midbrain (superior colliculus) and leaves the skull from the superior orbital fissure

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13
Q

inside the third nerve what is each muscle innervated by

A

each muscle is innervated by the corresponding sub nucleus

all subnuclei innervate ipsilateral muscles

except from the superior rectus sub nucleus and the central caudal nucleus

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14
Q

what does the central central caudal nucleus innverate

A

the levator palpable superior

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15
Q

what does a lesion at the central caudal nucleus result in

A

central caudal nucleus (CCN) supplies both levator muscles

lesion results in bilateral ptosis

with and without superior rectus limitation

if bilateral limitation of elevation

  • lesion affecting superior rectus sub nucleus
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16
Q

what are fasicualr lesions of the third cranial nerve

A

fascicular = whilst the nerve is travelling within the brainstem

if there is a unilateral limitation of elevation not the superior rectus subnucleus

involvement of the superior reectus nerve fascicles (axons after leaving the nucleus)

because axons from 1 superior rectus subnuclueu cross and pass through cintrlaterla as well as ipsilateral subnucleus

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17
Q

describe the course of the trochlear nerve

A

originates in the midbrain

only cranial nerve to exit from the posterior midbrain

smallest cranial nerve (by number of axons)

longest intracranial course

unable to distinguish between nuclear and fascicular lesions

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18
Q

describe the course of abducens nerve (6th)

A

rginates in the lower pons in the floor of the fourth ventricle lateral to the medial longitudinal fasiculus

nerves exits at the junction of the medulla and the pons

it then courses over the medial petrous per towards the cavernous sinus

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19
Q

what are the 6 syndromes of the sixth cranial nerve

A

the brainstem syndrome

elevated intracranial pressure syndrome

the petrous apex syndrome

the cavernous syndrome

the orbital syndrome

the isolated 6th (microvascular) - petrous apex = raised intracranial pressure

20
Q

what are the nuclear lesions of the 6th nerve palsiee

A

horizontal gaze palsy

ipsilateral lateral rectus and contrlateral medial rectus affected

this is because the 6th nucleus lies lateral to the medial lateral fasiculus

some neurones project to the medial lateral fasiculus

cross over to contralateral side and innervate contralateral medial rectus sub nucleus

21
Q

what would a fascicular lesion of the 6th nerve result in

A

an ipsilateral lateral rectus palsy

22
Q

what are the types of brainstem syndromes

A

webers syndrome

beendigst syndrome

fovilles syndrome

millard gubler syndrome

23
Q

what can multiple cranial nerve involvement result in

A

can be caused by lesions such as

infarction haemorrhagage

tumour

deymyelination

trauma

24
Q

what is colliers sighn

A

unilateral or bilateral eyelid retraction due to midbrain lesions

25
Q

what is a characteristic feature of the dorsal midbrain syndrome

A

characteristic feature of the dorsal midbrain syndrome (Parinaud Syndrome) could be assessed on upward gaze palsy

convergence retraction nystagmus

convergence retraction nystagmus - upward and inward beating when own drum is postiioned downwards

bilateral lid retraction (colliers sign)

light near dissociation

26
Q

what is webers syndrome

A

midbrain stroke syndrome

lesion in the midbrain affecting

3rd nerve fascicles

cerebral penducels

27
Q

what are signs of webers syndrome

A

ipsilateral 3rd nerve palsy

contralateral hemiparesis - weakensss to one Side of the body

28
Q

what is beneddikts syndrome

A

paramedian midbrain syndrome

lesion in the midbrain affects

3rd nerve fascicles

red nucleus

cerebral peduncle

29
Q

what are signs of Benedikts syndrome

A

ipsilateral 3rd nerve palsy

contralateral hemiparesis

contralateral ataxia with hypeerkinesis/tremor

30
Q

what is fovilles syndromee

A

lesion affects

abducens nucleus

ventral (anterior) pons

pyramidal tracts

31
Q

what are signs of fovilles syndrome

A

ipsilateral 6th nerve nuclear palsy

ipsilateral horizontal gaze palsy

ipsilateral facial palsy

contralateral hemiparesis

32
Q

what are signs of Millard gubler syndromees

A

lesion affects the base of pons anteroom medially affecting 6th and 7th nerve fascicles

pyramidal tracts

signs= espy;ateral 6th nerve palsy

ipsilateral facial nerve palsy (7th cranial nerve )

contralateral hemiplegia

33
Q

what is divergence paralysis

A

poorly understood
theories=
a divergence centre in brainstem and around 6th nerve nucleus

lesion of cerebellum or Arnold chairi malformation -which is the blockage of cerebral spinal fluid

34
Q

what are the signs of divergence paralysis

A

convergent deviation

homonymous diplo[ia

normal om- full abudction either eye

absent negative fusion amplitude

35
Q

what is the ateioloy of divergence paralysis

A

aetiology raised ice , ms , encephalitis , trauma , miller fisher syndrome

36
Q

what is the differential diagnosis for divergence paralysis

A

differential diagnosis= 6th nerve palsy

concomitant et

convergence spasm

treatment - may resolve on observation

occlude/ base out prisms

lateral rectus resections

37
Q

what diseases affect brainstem ocular motility function

A

Parkinson’s disease- limited upgaze

Huntingdon’s disease

Wernicke’s encephalopathy

Whipple’s disease

Arnold-Chiari malformation

38
Q

what is Parkinsons disease

A

Degenerative condition of CNS due to insufficient production of dopamine - mainly affects substantia nigra in BS

Causes: idiopathic (main), viral, inherited, trauma, drug induced

Rigidity, tremor, slow movements (cognition, mood and sleep can
also be affected)

Medication can help in short term but effect reduces over time and no cure

39
Q

what are the features of Parkinson’s disease

A

Ocular features…
Limited upgaze
Downgaze might be affected later
Hypometric saccades
Convergence insufficiency
Nystagmus
Reduced control of phoria – diplopia
Impaired smooth pursuit
Blepharospasm
Lid lag

40
Q

what is Huntingtons disease

A

Hereditary disorder of CNS

Substantia nigra in BS may be involved or pre-nuclear (e.g. Frontal eye fields or superior colliculus)

Loss of mobility, difficulty with speech and swallowing

Ocular features
Difficulty initiating saccades
Slow saccades
Impaired smooth pursuit

enlargement of the frontal horns

41
Q

what is wernike - Korsakoff encephalopathy

A

Spectrum of disorder caused by thiamine (B1) deficiency

Common in alcoholics but can also occur in gastric disorders e.g. Crohn’s disease

Gait ataxia, confusion, impaired short term memory

Treat with thiamine injections but can progress to Korsakoff’s syndrome

42
Q

what is the difference between wernike and Korsakoff

A

Wernicke (acute, reversible) - Korsakoff (chronic, irreversible)

43
Q

what are the ocular features of wernicke - korsakoff encephalopy

A

Ocular features:
Weakness of abduction
Gaze-evoked nystagmus
INO
Vertical nystagmus
Horizontal/vertical gaze palsies
May progress to complete ophthalmoplegia

44
Q

what is wipes disease

A

Caused by Tropheryma whippelii bacteria

Systemic disorder: weight loss, diarrhoea, gastro-intestinal bleeding, painful joints, arthritis, fever, fatigue, anaemia

Treated with antibiotics, although bacteria can remain in CSF

Can be fatal if left untreated

Ocular features
Reduced vertical saccades
Vertical and horizontal gaze palsies
Pendular oscillations

45
Q

what is Arnold chiari malformation

A

Anomaly in which cerebellar tonsils are displaced downwards towards foramen magnum –base of skulland may herniate

Congenital or acquired

Headaches, neck pain, tinnitus, nausea, facial pain, muscle weakness, sleep apnea, difficulty swallowing, impaired co-ordination, rapid heart beat, dizziness, fainting, thirst, chronic fatigue, paralysis in severe cases

46
Q

what are the ocular features of the Arnold chiari malformation

A

Ocular features
Various types of nystagmus but typically downbeat
Impaired pursuit
Impaired OKN
Concomitant ET
Divergence paralysis
Skew deviation
INO

47
Q
A