B6.044 Prework 1: MS Symptoms and Diagnosis Flashcards

(36 cards)

1
Q

central symptoms of MS

A

fatigue
cognitive impairment
depression
unstable mood

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

visual symptoms of MS

A

nystagmus
optic neuritis
diplopia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

speech symptoms of MS

A

dysarthria

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

throat symptoms of MS

A

dysphagia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

MSK symptoms of MS

A

weakness
spasms
ataxia
loss of balance

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

sensation symptoms of MS

A

pain
hypoesthesias
paraesthesias (tingling)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

bowel symptoms of MS

A

incontinence

diarrhea or constipation

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

urinary symptoms of MS

A

incontinence

frequency or retention

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

primary factors influencing diagnosis of MS

A

no single test
based on clinical exam, history, lab tests, and MRI
based on lesions being disseminated in time and space

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

criteria for MS diagnosis

A

McDonald Criteria

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

importance of early/effective treatment of MS

A

limits permanent damage to the CNS

may slow or prevent conversion to a more progressive form

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

2 clinical attacks

2 lesions with objective clinical evidence

A

no other data needed

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

2 clinical attacks

1 lesions with objective clinical evidence

A

need dissemination in space demonstrated by an additional clinical attack implicating a different CNS site or by MRI

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

1 clinical attacks

2 lesions with objective clinical evidence

A

dissemination in time demonstrated by an additional clinical attack by MRI
OR
demonstration of CSF specific oligoclonal bands

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

1 clinical attacks

1 lesions with objective clinical evidence

A

need dissemination in space demonstrated by an additional clinical attack implicating a different CNS site or by MRI
AND
dissemination in time demonstrated by an additional clinical attack by MRI
OR
demonstration of CSF specific oligoclonal bands

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

4 types of MS

A
relapsing remitting (85%)
secondary progressive (50% of relapsing remitting patients within 15 years)
primary progressive (15%)
progressive relapsing (?)
17
Q

what is a relapse

A
  • monophasic clinical episode with patient reported symptoms and objective findings typical of MS
  • represent focal or multifocal inflammatory demyelinating event in the CNS developing acutely or subacutely
  • duration of at least 24 hours
  • with or without recovery
  • absence of fever or infection
18
Q

relapsing and remitting course

A

characterized by relapses with stable neurological disability between episodes

19
Q

sequence of events in a relapse

A

symptoms develop over hours to days
symptoms can continue worsening for several weeks
symptoms slowly subside over weeks to months
residual symptoms can be present

20
Q

definition of progressive MS

A

steadily increasing objectively documented neuro disability independent of relapses
fluctuation, periods of stability, and superimposed relapses might occur

21
Q

events in progressive MS

A

gradual progression

often involves asymmetric leg weakness, ataxia, and spasticity

22
Q

diagnostic criteria of progressive MS

A
  1. one year of disease progression
    PLUS 2 of the 3:
    -evidence for DIS in the brain based on >1 T2 lesions in at least 1 area characteristic for MS
    -evidence for DIS in spinal cord based on >2 T2 lesions in the cord
    -positive CSF for oligoclonal bands and/or elevated IgG index
23
Q

different activity levels of progressive MS

A

active with progression (relapses and clinical deterioration not due to relapses)
active but without progression (relapses but no clinical deterioration)
not active but with progression
not active and without progression (stable)

24
Q

what is clinically isolated syndrome

A

first presentation of neuro symptoms lasting at least 24 hours
caused by inflammation and/or demyelination
can be monofocal or multifocal
partial or complete recovery
high chance of developing MS

25
etiology of initial relapses in relapsing-remitting disease
frequent inflammatory events that reach over the clinical threshold
26
axon loss in relation to MS
early axon loss occurs does not correlate with inflammation clinical disability over time parallels axonal loss axonal loss > clinical threshold initiated secondary progressive disease course
27
what can cause axonal loss
cyclical demyelination and remyelination events
28
appearance of MS lesions on T2 MRI
white lesions appear fluffy can appear in white matter, corpus callosum, and spinal cord
29
appearance of MS lesions on T1 MRI
IV admin of Gd reveals focal areas of BBB disruption | identified as high signal intensity regions
30
cortical lesions in MS
can occur early and may have some relationship with cognitive impairment and physical disability some cortical lesions observed by pathological examination are not detectable by MRI
31
spinal cord lesions
sensory and motor deficits on one or both sides below the lesion
32
brainstem lesions
diplopia, ataxia, weakness, altered sensation of the face
33
optic nerve lesions
blurry vision | painful eye movements
34
cerebral lesions
most common cause least amount of symptoms many are silent if very large: numbness or weakness or other cortical function
35
better prognostic factors for RRMS
``` female younger age white monofocal onset minimal cortical pathology onset w optic neuritis or isolated sensory symptoms low relapse rate high degree of remission after 1st relapse long interval to 2nd relapse mild relapse early ttx absence of oligoclonal IgG or IgM bands low disability at 5 years low lesion load on MRI ```
36
worse prognostic factors for RRMS
``` male older age nonwhite multifocal onset early cortical pathology onset w motor, cerebellar or bladder/bowel symptoms high relapse rate short interattack latency short interval to 2nd relapse severe relapse late ttx presence of oligoclonal IgG or IgM bands disability at 2 or 5 years abnormal MRI ```