Multiple sclerosis Flashcards

1
Q

Define multiple sclerosis

A

Demyelination of the CNS. MS can’t be diagnosed by one episode-> episodes have to be ‘disseminated by time and space’

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2
Q

Which cells are affected in multiple sclerosis?

A

Oligodendrocytes (CNS myelinating cells)

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3
Q

What type of hypersensitivity reaction is MS?

A

Type 4

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4
Q

Describe pathophysiology for MS

A
  • Molecular mimicry
  • Initial infection-> the antigen is
    recognised by T helper cells, after infection the myelin is recognised as an antigen leading to
    cytokines being released and antibodies being formed
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5
Q

What are the risk factors/causes for MS?

A
  • Female 20-40 (white)
  • Autoimmune disease
  • Family history
  • EBV
  • Genetic (HLA-DR2)
  • Low vitamin D
  • Smoking
  • Obesity
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6
Q

What are the different types of MS?

A
  1. Relapsing-remitting
  2. Primary progressive
  3. Secondary progressive
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7
Q

Describe relapsing-remitting MS

A

Symptoms -> incomplete recovery -> symptoms

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8
Q

Describe primary progressive MS

A

Gradual degeneration without recovery

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9
Q

Describe secondary progressive MS

A

Relapsing remitting –> primary progressive
- 75% of R-R cases evolve into this

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10
Q

What is the 1st presenting sign of MS?

A

Optic neuritis

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11
Q

What are other symptoms of MS?

A
  • Paraesthesia
  • Blurred vision
  • Uhthoff’s phenomenon
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12
Q

What is Uhthoff’s phenomenon?

A

Symptoms are exacerbated with heat eg. after a shower

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13
Q

What are the signs of MS?

A
  • Optic neuritis (inflamed optic nerve, can’t see red properly)
  • Internuclear ophthalmoplegia (lateral gaze impaired, damaged medial longitudinal fasciculus)
  • Brainstem signs
  • Sensory signs
  • UMN signs (not LMN)
  • Lhermitte phenomenon (electric shock sensation w/ neck flexion)
  • Charcot neurological triad
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14
Q

What is Charcot’s neurological triad?

A
  • Dysarthria (scanning or staccato speech)
  • Nystagmus
  • Intention tremor
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15
Q

How do you diagnose MS?

A

McDonald criteria
- 2 or more attacks disseminated in time (separate) + space (different part of CNS affected

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16
Q

What investigations do you do for MS?

A

MRI brain + cord
LP (lumbar puncture)
Delayed conduction speeds

17
Q

What is seen on MRI for MS?

A

Dissemination in SPACE (where is white demyelination?) + TIME (give gadolinium contrast to show long they’ve been there for)

18
Q

What is seen on LP for MS?

A

May see oligoclonal IgG bonds (non specific), increased lymphocytes

19
Q

What is the treatment for MS?

A
  • Acutely (in episodes) - IV or oral methylprednisolone for 3 days
  • Prophylaxis - β interferon (DMARD, biologic) (also inflixamab)