CM-BS & CN in Relation to Multiple Sclerosis Flashcards

1
Q

Brain Stem

A

Includes medulla, pons, and mesencephalon (midbrain)
Extends from pyramidal decussation the posterior comissure
Cranial nerves 3 to 12
blood supply vertebrobasilar system
Reticular formation as its central core integrating center of CNS as it receives collaterals from most AFFERENT

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2
Q

Brainstem reflexes

A

Pupillary light reactions (2+3)
Doll’s eye movement (3,4,6+8)
Corneal reflex (5+7)

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3
Q

Functionally distinct ascending and descending tracts are spread along the

A

transverse axis

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4
Q

Functionally distinct cranial nerve nuclei are spread along the

A

rostrocaudal axis

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5
Q

Long tract signs occur

A

Contralateral to the lesion

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6
Q

Cranial nerve signs occur

A

Ipsilateral to the lesion

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7
Q

OculOmOtOr and trOchlear nuclei

A

Diplopia (dbl vision)
Ipsilateral pupillary disturbance with ptosis (oculomotor
n. )
level of MIDBRAIN

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8
Q

Abducens nucleas and facial nucleus

A

Diplopia (abducens)
Ipsilateral facial weakness (facial n.)
level of PONS

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9
Q

Nucleus ambiguus (CN9/10/12)

A

DORSAL nucleus of VAGUS and HYPOGLOSSAL nucleus
Disturbnce of : speech/swallowing
level of MEDULLA

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10
Q

Corticospinal tract

A

Hemiplegia on the opposite side of the lesion

MEDIAL TO BRAINSTEM

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11
Q

Medial leminiscus

A

Loss of vibration and position sensation on the opposite side of the lesion
MEDIAL TO THE BRAINSTEM

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12
Q

Spinothalamic tract

A

Contralateral loss of PAIN AND TEMP sensation

LATERAL to brainstem

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13
Q

Descending sympathetic fibers

A

Horners syndrome : ptosis and miosis

Lateral locatiom

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14
Q

MS

A

T cells cause demyelination and destruction of axons in WHITE MATTER/CEREBRAL CORTEX ( I guess grey matter also )

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15
Q

CAUSES OF MS

A
identical twins 25%
WHITE 
WOMEN x2 than men
Low immunity
Risk increases w distance from equator
Geographic risk is equal after age 15
Western : HLADR15/DQ6
Kuwait : DR4
Epstein barr virus INFECTION
Metabolic : low sunglight (UV-B)
Low vit D (interacts w HLA DR15)
Toxins : smoking
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16
Q

Diagnosis of MS

A

Clinical
MR
Lumbar puncture ( examins oligoclonal bands in CSF)
Visual evoked potentials

17
Q

Prevalence of MS

A

prevalence : 100/150 per 100,000
Incidence : 7/100,1000
Wordwide 2.5 mill have MS

18
Q

Primary vs 2ndry progressive MS

A

Primary : from the beginning, symptoms gradually develop and worsen over time (10-15%)
2ndry :follows on from relapsing/remitting worsening symptoms (50%)

19
Q

Clinical features of MS

A

Brainstem/Cerebellar (20%)
Oculomotor : diplopia
Speech probs ( dysarthria ) / swallowing ( dysphagia )
Vertigo, nausea, vomitting, unsteadiness (ataxia)
Facial numbness & weakness
Paroxysmal symptoms : trigeminal neuralgia, tonic spasm
LEGS ARE AFFECTED MORE THAN ARMS > ASYMMETRIC
Lhermitte’s sign: Unpleasant sensation in the back, and radiating
into leg on flexing the neck

20
Q

Inter nuclear ophthalmoplegia (INO)

A
Lesion of  the medial
longitudinal fasciculus
(MLF) and causes
diplopia • In left INO:
– Impairment of
adduction of  the left
eye – Nystagmus of  the
right abducting  eye
 Causes:
– Multiple sclerosis
– Stroke
– Vasculi tis
21
Q

Oculomotor nerve palsy

A
  1. Aneurysm of the post communicating artery : compress the superficial parasympathetic pupiloconstrictor fibers-dilated pupil
  2. Uncal herniation : increased intracrianial P. 2ndry to space occupying lesion (tumor, absces, hemorrhage)
  3. Cavernous sinus thrombosis
  4. Midbrain infarction