Demyelinating Disorders Flashcards

1
Q

are the axons preserved in demyelination?

A

yes

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2
Q

give examples of primary demyelinating disorders

A

MS, GBS (a few other obscure one, some occur post-infection)

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3
Q

give examples of secondary demyelinating disorders

A

central pontine myelinosis, viral, toxic, GPA, sarcoid, lyme, HIV, SLE

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4
Q

when does central pontine myelinosis occur

A

over rapidly corrected hyponatraemia

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5
Q

what condition is guillian barre associated with

A

few weeks after campylobacter infection (also other infections)

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6
Q

what is the presentation of guillian barre

A

acute
pain
ascending/proximal weakness
then paresis

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7
Q

management of guillian barre

A

IV immunoglobulin

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8
Q

HLA DRB1 is associated with which demyelinating disorder

A

multiple sclerosis

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9
Q

risk factors for multiple sclerosis

A

female
north
vit d
FH

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10
Q

what is the pathology of urinary problems in multiple sclerosis

A

detrusor sphincter dyssynergia

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11
Q

what is the pathology of multiple sclerosis

A

inflam demyelinating plaques, pyramidal dysfunction

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12
Q

in multiple sclerosis, what do active plaques become?

A

gliotic scars

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13
Q

name the 4 types of multiple sclerosis

A

relapsing remitting
primary progressive
secondary progressive
progressive relapsing

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14
Q

GO STUDY THE GRAPH OF THE CLINICAL COURSE OF THE TYPES OF MS

A

DO IT

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15
Q

commonest age range for multiple sclerosis onset

A

30-40

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16
Q

what eye problems can MS cause

A

optic neuritis

internuclear ophthalmoplegia

17
Q

how would optic neuritis present generally

A

acute pain RAPD

18
Q

how would internuclear ophthalmoplegia present

A

ipsilateral can’t adduct

contralateral nystagmus

19
Q

what is Lhermitte’s sign

A

in MS, electric shock sensation going down spine

20
Q

MS in the cerebellum can cause Charcot’s triad, what is this? other signs incl nystagmus, dysdiadokinesis

A

ataxia + intention tremor + dysarthria

21
Q

MS causing spasticity, increased tone, weak upper limb extensors and lower limb flexors indicates a lesion in the…

A

pyramidal tract

22
Q

MS causing a VI or VII palsy indicates a lesion in the…

23
Q

investigations for MS

A

T2 weighted MRI + contrast
LP CSF
EEG
serology/renal/liver profile

24
Q

what is seen on MRI in ms

A

hyperintense white matter lesions

25
what CSF abnormalities are present in MS
lymphocytes+ IgG oligoclonal band
26
what blood abnormalities are present in MS
none
27
diagnostic criteria for MS
>2 clinical/MRI episodes suggesting demyelination in separate time+ place
28
what is seen on evoked potential tests in MS
slowed conduction
29
what is the acute management of mild MS
symptomatic
30
what is the acute management of moderate MS
PO CCS
31
what is the acute management of severe MS
admit + IV CCS
32
what is the 1st line disease modifying management of relapsing remitting MS
SC/IM interferon beta
33
management of spasticity in MS
baclofen, tizanidine
34
management of urinary symptoms in ms
anticholinergic oxybutynin
35
management of optic neuritis in MS
IV methylpred then PO CCS