Case of paralysed person Flashcards

1
Q

definition of MS?

A

chronic immune mediated CNS disease

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2
Q

how many people is MS affecting?

A

2 million

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3
Q

who does MS usually affect?

A

female predominance age 20-40

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4
Q

increased risk association with MS?

A

low vit D/ exposure UVB
EBV infection in past
obesity/ smoking
HLA DRB1
HLA-A

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5
Q

pathology of MS?

A

multifocal neuroinflammation plaques in white matter peri venular , subcortical and grey matter

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6
Q

molecular level of MS?

A

infiltrating lymphocytes mainly T cells,
axon degeneration gliosis and oligodendrocyte damage

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7
Q

how is MS first triggered

A

peripheral t cells become reactive, cross reactivity foreign antigens to CNS antigens carried in lymphatic system.
Activate macrophages and glia

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8
Q

how would a MS brain look macroscopically?

A

white matter loss- corpus callosum
hydrocephalus
volume loss global atrophy

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9
Q

what happens to bbb?

A

vasoactive molecules make the brain more leaky

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10
Q

what happens after some time?

A

remyelination via the oligodendrocyte precursor cells by myelin is thinner

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11
Q

how does GM to WM differ

A

GM lesions have less b/t cells or macrophage, seeding of inflammatory cells

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12
Q

what causes MS damage?

A

inflammatory demyelination (new T2 lesions/ or clinical relapse) and progressive neurodegeneration(atrophy/disability markers worsen irrespective of relapse activity)

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13
Q

scale for MS to assess mobility?

A

expanded disability status scale

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14
Q

SPMS?

A

less relapse favour progression but new plaques on MRI
PIRA>6-12 months

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15
Q

e

A

IFNbeta siponimod

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16
Q

PPMS?

A

predominant progression from onset
typically spastic paraparesis or sensory cereballar ataxia

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17
Q

radiologically isolated syndrome?

A

MRI abnormaties without clinical signs
40% will develop MS

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18
Q

Clinically isolated syndrome

A

symptoms lasting more than a day, demyelination optic neuritic

19
Q

what is macdonald criteria?

20
Q

how to diagnose MS?

A

at least 1 clinical relapse corresponding to one demyelinating MRI lesion

21
Q

differential diagnosis of MS?

A

ADEM, NMOSD, sarcoidosis,SLE

22
Q

what can you find in MS investigations?

A

oligoclonal bands positive

23
Q

LMN signs

A

weakness, reduced reflexes, reduced tone flaccidity

24
Q

UMN signs

A

increased brisk reflexes, increased tone,

25
where does the cell body of lmn sit?
anterior horn of grey matter
26
upper motor neurons cause?
paraplegia
27
if lmn lesion ask?
is sensation affected
28
if sensation is normal then?
NMJ, muscle
29
if sensation is abnormal then?
root, nerve, neuropathy
30
upper motor lesion investigation?
mri
31
if NMJ and muscle affected?
check for Myasthenia gravis and electrodes
32
in spinal cord lesion what is affected?
flaccidity/ hypotonia at that level- LMN upper motor neurons - weakness spasticity distal to the lesion
33
T1 vs T2?
fluid is bright on T2, and black on T1
34
demyelination on MRI is?
white matter lesions typically
35
biomarkers of acute neuroinflammation?
t1 lesions with contrast enhancement
36
ring enhancing lesion on MRI could indicate?
brain abscess
37
what can you see in MS?
perpendicular lesions to ventricles, discrete (can draw around)
38
spinal cord lesions are usually?
dorsal, lateral eccentric
39
what is a precursor of MS?
transverse myelitis
40
tumefactive MS?
incomplete ring, peripheral enhancement
41
acute disseminated encephalomyelitis?
multiple lesions all over, patient very sick flu like illness
42
neuromyelitis optica?
demyeliniation long spinal cord lesion affects optic nerve too
43
MS differentials?
aging- a white dot per decade is normal vascular- fluffy ms- dorsal fingers