Multiple Sclerosis Flashcards

1
Q

Multiple Sclerosis

A

presumed autoimmune demyelinating disorder of the central nervous system

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2
Q

Who “gets” MS?

A
  • Generally occurs in younger females (20-50 yo) of Northern European descent
  • However risk seems to increase with distance from the equator
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3
Q

Is MS a “genetic disease?”

A

• Genetic contribution but not a “genetic disease”

– Certain HLA markers and single nucleotide polymorphisms (SNPs) increase risk

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4
Q

Suspected environmental triggers of MS

A

– Viral Exposures (EBV)

    • Tobacco exposure
    • Obesity/dietary factors?
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5
Q

Possible Pathogenesis of MS

A
  • T cells are activated, attach to, break down, and cross blood brain barrier to release interleukins
  • Ultimately causes demyelination
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6
Q

Syndromes Highly Suggestive of MS- Optic neuritis

A

– Decreased monocular vision (often involving central vision)
– Pain with eye movement
– Decreased red/green color
– Clinically associated with an afferent pupillary defect
– Uhthoff phenomeon (heat intolerance)

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7
Q

Brainstem Syndromes Highly Associated with MS

A
– Internuclear ophthalmoplegia (MLF)
– Oculomotor dysfunction
– Trigeminal Neuralgia
– Facial nerve palsy
– CST/upper motor neuron involvement
– Ataxia
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8
Q

Syndromes Highly Suggestive of MS- Spinal Cord Syndrome

A

– Transverse myelitis
– Lhermitte’s “sign”
– Numbness/sensory level
– Deafferented hand
– Urinary urgency, incontinence, erectile dysfunction
– Progressive asymmetric spastic paraplegia

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9
Q

“Silent” Symptoms of Multiple Sclerosis

A
  • Fatigue
  • Bladder dysfunction
  • Sexual dysfunction
  • Spasticity
  • Pain
  • Cognitive impairment
  • Bowel dysfunction
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10
Q

Six Essential Criteria for “Definite Multiple Sclerosis”

A
  • Objective abnormalities on examination
  • Evidence on exam of 3 or more separate parts of CNS
  • Objective evidence must reflect predominantly while matter involvement
  • Involvement of the neuroaxis must occur temporally (2 or more episodes, slow, step wise gait)
  • Age 10-50
  • Cannot be better explained by another process
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11
Q

The diagnosis of MS is ultimately a

A

combination of a clinical diagnosis with radio-graphic corroboration

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12
Q

What is a concerned risk of MS therapies?

A

Progressve Multifocal Leukoencephalopathy

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13
Q

How are MS relapses treated?

A
  • Goal is to speed recovery & limit injury
  • Steroids
  • ACTH
  • Plasmapharesis
  • IVIg
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14
Q

Symptoms of MS

A
  • Fatigue
  • heat intolerance
  • cognitive deficits: multitasking, recall, concentration
  • spasticity
  • depression
  • bladder dysfunction
  • pain
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