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…

A

brainstem

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
Q

what CSF abnormalities are present in MS

A

lymphocytes+ IgG oligoclonal band

26
Q

what blood abnormalities are present in MS

A

none

27
Q

diagnostic criteria for MS

A

> 2 clinical/MRI episodes suggesting demyelination in separate time+ place

28
Q

what is seen on evoked potential tests in MS

A

slowed conduction

29
Q

what is the acute management of mild MS

A

symptomatic

30
Q

what is the acute management of moderate MS

A

PO CCS

31
Q

what is the acute management of severe MS

A

admit + IV CCS

32
Q

what is the 1st line disease modifying management of relapsing remitting MS

A

SC/IM interferon beta

33
Q

management of spasticity in MS

A

baclofen, tizanidine

34
Q

management of urinary symptoms in ms

A

anticholinergic oxybutynin

35
Q

management of optic neuritis in MS

A

IV methylpred then PO CCS