demyelinating diseases Flashcards

0
Q

cause of MS

A

unknown- more inc ertain families- due to HLA Dr2

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1
Q

MS

A

multople inflammatory white matter lesions separated in space and time

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2
Q

Ms is an an immune attack on

A

oligodendroglia

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3
Q

single episode

A

cannot be diagnosed as MS-clinically isolated syndrome

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4
Q

patients with only one single location of damage

A

cannot be diagnosed with MS

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5
Q

4 tpyes of MS

A

relapsing remitting
secondarily progressive
primary progressive
rapidly progressive

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6
Q

MS often affects

A
optic nerves
dorsal columns
corticospinal tract
cerebellar pathways
medial longitudinal fasiculus
spinal trigem tract
control of bladder
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7
Q

Lhermitte’s sign

A

electric sensation down back and/or legs with neck flexion- irritation of cervical spinal cord sensory tracts

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8
Q

MS does NOT

A

damage neuron cell bodies
–does not result in LMN damage, c nerve nuclei dmage, damage to peripheral nerves

does not produce aphasia or effect memory cog until late

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9
Q

MRI shows

A

T2 hyperintensities in periventricular distribution in most

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10
Q

CSF shows

A

oligoclonal bands and elevated IgG

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11
Q

only MRI can show

A

whether lesions are isolated in time and space

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12
Q

relapsing remitting

A

1st incidence clinically isolated- like clinical neuritis

w/ each recurring episode, some increasing disability with a cumulative deficit

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13
Q

secondary progressive

A

starts out like relapsing remitting but then begins an upward slope of increasing neuro deficit in between the definite episodes

more aggressive, less responsive to treatment

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14
Q

primary progressive MS

A

no distinct episode of symptoms and no sudden onset

MRI and clinical over course of illness both by clinical picture

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15
Q

progressive relapsing

A

combo of progressive dsiability from beginnging with some relapses and remissions

16
Q

delay between onset of symptoms and diagnosis

A

3.5 years

17
Q

MS attac

A

actication helper T cells–>attracted to and adhere to blood vessels of BBB–>breakdown BBB and invaid–>encounter antigens of CNS and reactivate and attack CNS myelin

18
Q

fda approved treatment

A

high dose steroids-acute attack, doesnt alter course

chemo drugs- harsh effect (such as cardiomyopathy with mitoxantrone)

19
Q

natalizumab

A

recently approved, black box warning for causing progressive multifocal leukencephalohy–screen for JC virus antibodies

20
Q

B interferon

A

modulates t cell and b cell fx
decreases expression of matrix metalloproteinases
reverses BBB disruption and alters expression of a number of cytokines

21
Q

glatiramer acetate

A

probs functions as an altered peptide ligand for the major histocompat complex class II molecules

stimulates reg t cells that have a propsensity for CNS migraton that may suppress immune rxn in cns