MS Flashcards

1
Q

MS is an autoimmune reaction against?

A

oligodendrocytes

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2
Q

In MS, what do you get destruction of?

A

myelin

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3
Q

are peripheral nerves affected?

A

no

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4
Q

normally, macrophages cannot easily cross the BBB, but what do they express that allows them to adhere and cross the endothelium?

A

glycoprotein α4 β1

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5
Q

show up on MRI as white blobs, roughly 2-10mm in size, and can occur anywhere in the CNS, although most commonly occur at the optic nerves, periventricular lesion, brainstem and cerebellar connections?

A

plaques

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6
Q

what is the most common form of MS?

A

relapsing remitting (RR)

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7
Q

what is uhtoffs phenomenon?

A

symptoms worse during increased heat - conduction slows with increased heat

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8
Q

most common presenting symptom?

A

fatigue/lethargy

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9
Q

what is lhermittes sign?

A

on flexion of the neck, there is an electric shock sensation down the spine and into the limbs

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10
Q

what are upper motor neurone signs?

A

spasticity, weakness, brisk reflexes

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11
Q

what do oligoclonal bands show?

A

there is lots of antibody to something in the CSF - there will be oligoclonal bands in 80% of cases

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12
Q

for diagnosis, you need at least 1 attack and multiple plaques on MRI

A

y

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13
Q

often used as symptomatic treatment. It is an antagonist of GABA receptor ?

A

Baclofen

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14
Q

how do you manage urinary incontinence?

A

oxybutanin or self catheterisaton

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15
Q

a condition affecting the movement of the eyes which is characteristic of MS?

A

internuclear opthalmoplegia

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16
Q

in INO, when patient looks to left what happens?

A

let eye is fine, right eye does not go past midline

17
Q

in INO, when patient looks to right what happens ?

A

right eye is fine, left eye does not go past midline

18
Q

what is the definitive investigation in MS?

A

MRI

19
Q

in visual evoked potentials, a delayed response indicates what?

A

there is evidence of some sort of optic nerve lesion

20
Q

what other conditions can mimic lesion on MRI?

A

sarcoidosis, SLE, bechets syndrome

21
Q

what is the severity of the disease like ?

A

Some patients may be able to live normally for many years, whilst other will becomes severely disabled.

22
Q

female to male?

A

f:m 3:1

23
Q

what pyramidal dysfunction ?

A

increased tone, spasticity and weakness

24
Q

weakness in arms and legs?

A

weakness in extensors in arms and flexors in legs

25
Q

you get loss of dorsal column. what does this cause?

A

proprioception and vibration (DEE PEE VEE)

26
Q

you get pain and paraesthesia

A

y

27
Q

what cerebellar defects can you get?

A

ataxia

28
Q

what criteria is used for diagnosis?

A

mcdonalds

29
Q

to satisfy dissemination in place, you need?

A

objective evidence of neurological deficits localised in two sepatrate parts of the CNS

30
Q

for dissemination in time, you need?

A

onset of neurological deficits separated by at least one month

31
Q

what are blood tests like in MS?

A

negative

32
Q

for spastcity, what can you give?

A

BT - baclofen or tizanidine. or botulinum toxin

33
Q

For sensory symptoms, can give?

A

sense maga

amytriptyline or gabapentin

34
Q

for urinary symptoms of frequency etc. tx?

A

Bladder drill, anticholinergics eg oxybutanin,desmopressin and catheterisation

35
Q

for fatigue?

A

Amantadine and modafinil (amanmod)

Hyperbaric oxygen

36
Q

First line therapy

A

Interferon Beta – avonex,rebif, betaseron,extavia

Glitiramer acetate

Techfedira

37
Q

Second line therapy

A

Monoclonal antibodies tysabri, lemtrada, zymbrata

Fingolimod

38
Q

Third line

A

mitoxantrone

39
Q

S1P modulator ?

A

fingolimod