Lecture 64: Multiple Sclerosis Flashcards

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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
Q

Where do lesions always call symptoms?

A

Spinal cord, optic nerve (shallow end)

26
Q

Where do lesions rarely cause symptoms?

A

Juxtacortical, periventricular (deep end)

27
Q

Where do lesions sometimes cause symptoms?

A

Brainstem, cerebellum

28
Q

What happens over time with MS?

A

The reserve is decreased (loss of neurons), eventually the many lesions come to light