Lecture 64: Multiple Sclerosis Flashcards

1
Q

Typical MS lesion sites/symptoms (4)

A

Monocular vision loss, brainstem syndromes (cranial nerve deficits), spinal cord = motor/sensory impairments, imbalance

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2
Q

Early features

A

Motor weakness, paresthesias, impaired vision, double vision, intention tremor, ataxia

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3
Q

T/F: Diagnosis of MS is certain initially

A

False! One lesion location is hard to diagnose

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4
Q

How do you recognize MS early?

A

MRI!

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5
Q

Original triad for MS presentation and where they localize. How do we feel about this now?

A

Intention tremor, nystagmus, scanning speech (WM pathways to and from cerebellum); we now try to treat LONG BEFORE its gotten this far

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6
Q

What is the most common place for MS lesion? Name of disease and presentation.

A

Optic nerve; neuritis; painful gradual (days) loss of vision in ONE eye often with scotoma of central vision

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7
Q

How often do you see optic edema? How many patients w/ optic neuritis get better completely? How many will end up with MS?

A

50%; 33%; 50%

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8
Q

Four CRITICAL clinical patterns of MS. Does a patient always have just one?

A

Relapsing remitting; secondary progressive; primary progressive; progressive relapsing; NO–secondary progressive FOLLOWS relapsing-remitting

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9
Q

Relapses get more/less frequent over time

A

Less frequent

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10
Q

Describe secondary progressive disease

A

Starts w/ relapses, but then continues to progress (more disability) over time w/ or w/out relapses

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11
Q

Do lesions always coordinate with symptomology?

A

Nope! Can have many new lesions w/out new symptoms

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12
Q

% patients who begin with RRMS, % who will go into secondary-progressive

A

85%; 50% (NATURAL HISTORY, NOT W/ TREATMENT)

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13
Q

Epidemiology of MS (age, gender, race, location)

A

20-40; 2-3 x women; N European; more w/ northern exposure

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14
Q

Genes of MS

A

Higher risk in first degree relatives

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15
Q

Criteria in MS (name) and principle

A

McDonald Critera; look for evidence of dissemination in space and time

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16
Q

When you give dye…what lights up?

A

Areas of the nervous system that are actively inflamed, light up

17
Q

Classical MS lesions

A

Multiple, round, peri-ventricular WM

18
Q

Relationship b/t MS and lesions

A

MRI lesions predict development of MS after first attack

19
Q

What causes MS on a cellular level?

A

Inflammatory attack of oligodendrocytes by self-reactive T1 cells that cross compromised BB barrier

20
Q

Misguided T cells mistake…

A

Myelin for an antigen

21
Q

CSF in MS

A

Increased IgG synthesis rate and IgG oligoclonal bands (90% have them but we don’t know what they target)

22
Q

Under the microscope…

A

Inflammatory infiltrates in MS lesions

23
Q

Treating exacerbation

A

High dose IV steroids

24
Q

Goals of treatment (4)

A

Prevent relapse, prevent disability, clinical stability, decrease new lesions

25
Where do lesions always call symptoms?
Spinal cord, optic nerve (shallow end)
26
Where do lesions rarely cause symptoms?
Juxtacortical, periventricular (deep end)
27
Where do lesions sometimes cause symptoms?
Brainstem, cerebellum
28
What happens over time with MS?
The reserve is decreased (loss of neurons), eventually the many lesions come to light