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
what is a characteristic feature of the dorsal midbrain syndrome
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
what is webers syndrome
midbrain stroke syndrome lesion in the midbrain affecting 3rd nerve fascicles cerebral penducels
27
what are signs of webers syndrome
ipsilateral 3rd nerve palsy contralateral hemiparesis - weakensss to one Side of the body
28
what is beneddikts syndrome
paramedian midbrain syndrome lesion in the midbrain affects 3rd nerve fascicles red nucleus cerebral peduncle
29
what are signs of Benedikts syndrome
ipsilateral 3rd nerve palsy contralateral hemiparesis contralateral ataxia with hypeerkinesis/tremor
30
what is fovilles syndromee
lesion affects abducens nucleus ventral (anterior) pons pyramidal tracts
31
what are signs of fovilles syndrome
ipsilateral 6th nerve nuclear palsy ipsilateral horizontal gaze palsy ipsilateral facial palsy contralateral hemiparesis
32
what are signs of Millard gubler syndromees
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
what is divergence paralysis
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
what are the signs of divergence paralysis
convergent deviation homonymous diplo[ia normal om- full abudction either eye absent negative fusion amplitude
35
what is the ateioloy of divergence paralysis
aetiology raised ice , ms , encephalitis , trauma , miller fisher syndrome
36
what is the differential diagnosis for divergence paralysis
differential diagnosis= 6th nerve palsy concomitant et convergence spasm treatment - may resolve on observation occlude/ base out prisms lateral rectus resections
37
what diseases affect brainstem ocular motility function
Parkinson’s disease- limited upgaze Huntingdon’s disease Wernicke’s encephalopathy Whipple’s disease Arnold-Chiari malformation
38
what is Parkinsons disease
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
what are the features of Parkinson's disease
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
what is Huntingtons disease
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
what is wernike - Korsakoff encephalopathy
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
what is the difference between wernike and Korsakoff
Wernicke (acute, reversible) - Korsakoff (chronic, irreversible)
43
what are the ocular features of wernicke - korsakoff encephalopy
Ocular features: Weakness of abduction Gaze-evoked nystagmus INO Vertical nystagmus Horizontal/vertical gaze palsies May progress to complete ophthalmoplegia
44
what is wipes disease
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
what is Arnold chiari malformation
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
what are the ocular features of the Arnold chiari malformation
Ocular features Various types of nystagmus but typically downbeat Impaired pursuit Impaired OKN Concomitant ET Divergence paralysis Skew deviation INO
47