Multiple Sclerosis Flashcards

(47 cards)

1
Q

What is the process of demyelination?

A

a disruption of myelin, which is the coating around neurons

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2
Q

What produces myelin?

A

oligodendrocytes in the CNS

schwann cells in the PNS

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3
Q

What causes multiple sclerosis?

A

a disease of the CNS caused by an autoimmune attack on oligodendrocytes resulting in multiple areas of demyelination.

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4
Q

MS is one of the leading causes of what?

A

neurological disability in young adults

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5
Q

what are the risk factors of MS?

A

age, gender, genetics and environment

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6
Q

95% of those diagnosed with MS are in what age range?

A

15-55

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7
Q

What is the gender preference for MS?

A

females

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8
Q

What is the chance you will get MS if both of your patents have MS?

A

9%

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9
Q

What is the gene associated with the genetic component of MS?

A

HLA-DR2

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10
Q

What is an interesting caveat about where you live in regards to likelihood of MS?

A

individuals in the northern states have a 3x higher likelihood of developing MS then people in southern states. If someone moves before the age of 15, they will not carry the risk with them.

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11
Q

What are possible mechanisms of MS?

A

molecular mimicry and failure of colonal deletion

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12
Q

What is a hallmark of MS?

A

multiple scarred foci (plaques) with in the white matter of the CNS and perivenular inflammation

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13
Q

What happens when the myelin is disrupted?

A

decrease in saltatory conduction and action potentials are unable to be effectively transmitted down axons, leading to neurological dysfunction

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14
Q

What are the types of MS?

A

relapsing-remitting
primary progressive
secondary progressive
progressive relapsing

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15
Q

What is a clinically isolated syndrome?

A

1st episode of transient neurological dysfunction

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16
Q

What is relapsing remitting MS?

A

multiple episodes of transient neurological dysfunction which may or may not completely resolve. There is no progression between relapses.

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17
Q

What is primary progressive MS?

A

No defined relapse or remission. Disease progresses relentlessly from its onset

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18
Q

What is secondary progressive MS?

A

Patients with relapsing remitting MS may (after ~17 years) start to have some progression during relapses.

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19
Q

What is progressive relapsing MS?

A

relentless progression from the onset but may have a rare relapse

20
Q

What do we need to diagnose MS?

A

dissemination in time and space

can be fulfilled clinically or radiographically

21
Q

What are the common presenting signs and symptoms of MS?

A
limb sensory loss - 31%
visual loss - 16%
sub acute weakness
diploplia
gait disturbance
vertigo
acute weakness
22
Q

What are two common clinically isolated syndromes associated with MS?

A

optic neuritis and transverse myelitis

23
Q

Is there a correlation between treatment and clinically isolated syndromes?

A

treatment after clinically isolated syndromes is showing to result in better outcomes and less disability over time

24
Q

What is optic neuritis?

A

demyelination of the optic nerve

characterized by the triad of :
visual acuity loss
dyschromatopsia
epsilateral eye pain especially with movement

25
What does the neuro exam show for optic neuritis?
relative afferent pupillary defect
26
What does an MRI show for optic neuritis?
increased T2 signal of the optic nerve
27
What is the prognosis for optic neuritis?
good, complete or near complete recovery is expected
28
What is transverse myelitis?
demyelination of the spinal cord; any of the ascending or descending tracts may be affected
29
What are the typical symptoms of transverse myelitis?
sensory loss in one or both lower extremities often accompanied by a sense of heaviness.
30
What does the neuro exam show for transverse myelitis?
spasticity, at sensory level, up going goes, and weakness
31
What is commonly associated with transeverse myelitis?
L'hermitte's Phenomenon- a lightning like pain that radiates down spine with head antero flexion
32
In the physical exam what is seen with MS?
charcots triad: nystagmus, intention tremor, and scanning speech (staccato)
33
What are the diagnostic tests for MS?
LP, MRI(T2 and FLAIR) and visual evoked potentials
34
What is the only nerve myelinated by oligodendrocytes?
optic nerve
35
What is seen on a lumbar puncture in a patient with MS?
oligoclonal bands; This represents increased synthesis within the CSF of antibodies present in 95% of MS patients
36
What do visuallly evoked potentials show in a positive diagnosis of MS?
increased latency to visual stimuli
37
How do MS lesions typically appear on imaging?
periventricular (dawsons fingers) and ovoid
38
How do we treat acute exacerbations of MS?
IV methylprednisone- 3-5 days (does not affect the progression of the disease, just increases recovery time) *oral prednisone is a/w increased subsequent attacks
39
What is the disease modifying treatment for MS?
inteferon beta 1a inteferon beta 1b copaxone- random peptide chain of the most common AA in myelin
40
What is the prognosis of MS?
Good, 90% are independent 10 yrs after dx
41
What are signs of a good prognosis?
female, relapsing-remitting, and optic neuritis at onset with infrequent exacerbations
42
What is Guillian Barre Syndrome?
demyelination of PNS that is likely post infectious or post vaccination in nature present with a rapidly progressing symmetric, ascending limb paralysis
43
What are the main characteristics of Guillian Barre?
3A's: acute onset, ascending paralysis, areflexia
44
What can GBS lead to ultimatley?
Respiratory failure
45
What are the post infectious causes of GBS associated with?
GI illnesses from C. jejuni
46
What is the prognosis of GBS?
if caught early enough, full recover is expected
47
What is the treatment for GBS?
IV IG or plasmaphoresis