MS Flashcards

(39 cards)

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?

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?

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
you get loss of dorsal column. what does this cause?
proprioception and vibration (DEE PEE VEE)
26
you get pain and paraesthesia
y
27
what cerebellar defects can you get?
ataxia
28
what criteria is used for diagnosis?
mcdonalds
29
to satisfy dissemination in place, you need?
objective evidence of neurological deficits localised in two sepatrate parts of the CNS
30
for dissemination in time, you need?
onset of neurological deficits separated by at least one month
31
what are blood tests like in MS?
negative
32
for spastcity, what can you give?
BT - baclofen or tizanidine. or botulinum toxin
33
For sensory symptoms, can give?
sense maga | amytriptyline or gabapentin
34
for urinary symptoms of frequency etc. tx?
Bladder drill, anticholinergics eg oxybutanin,desmopressin and catheterisation
35
for fatigue?
Amantadine and modafinil (amanmod) | Hyperbaric oxygen
36
First line therapy
Interferon Beta – avonex,rebif, betaseron,extavia Glitiramer acetate Techfedira
37
Second line therapy
Monoclonal antibodies tysabri, lemtrada, zymbrata Fingolimod
38
Third line
mitoxantrone
39
S1P modulator ?
fingolimod