23. Multiple sclerosis Flashcards

1
Q

Definition of MS

A

Chronic, progressive, autoimmune, inflammatory disease of the CNS resulting in demyelination of nerves

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2
Q

Epidemiology of MS

A

30-40s
Female:Male 2:1

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3
Q

Etiology of MS

A

Unknown, but has a few risk factors:
- Genetic: HLA, fam. history
- Environmental: Virus, geographics (more towards the poles), vitamin D def.

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4
Q

Pathology of MS

A

T-cells (CD8+) activated in the periphery leads to apoptosis of oligodendrocytes (usually producing myelin) and secondary axon degeneration in the CNS. This leads to neurodegeneration of white- and grey matter –> brain atrophy

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5
Q

What are the demyelinated regions in MS called?

A

Plaques

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6
Q

Characteristics of active plaques in MS

A
  • BBB dysfunction
  • Perivascular infiltration of lymphocytes and plasma cells
  • Segmental demyelination
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7
Q

Characteristics of chronic plaques in MS

A

Scar tissue formation (sclerosis) due to astrocyte proliferation

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8
Q

Clinical signs of MS

A
  • Optic neuritis
  • Sensory: parasthasia, numbness
  • Motor: paresis
  • Cerebellar: limb/trunk ataxia, dysarthria, nystagmus, tremor, coordination/balance problems
  • Brainstem: gaze palsy, trigeminal pain
  • Internuclear ophthalmoplegia
  • Demyelination of spinal cord tracts
  • Autonomic dysfunction
  • Cranial nerve palsies
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9
Q

Characteristics of optic neuritis

A
  • Often first symptom of MS
  • Impaired vision
  • Painful
  • Unilateral
  • Colour blindness
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10
Q

Characteristics of Internuclear ophthalmoplegia

A

Gaze abnormality characterized by impaired horizontal eye movements with weak and slow adduction of the affected eye, and abduction nystagmus of the contralateral eye

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11
Q

Signs of demyelination of spinal cord tracts

A

Lhermitte sign: a shooting electric sensation traveling down the spine upon flexion of the neck.

Pyramidal tract lesion: upper motor neuron weakness, spasticity, hyperreflexia, positive Babinski sign, impaired gait

Dorsal spinal column lesion: loss of vibration and fine-touch sensation, numbness, paresthesias, sensory ataxia usually involving the trunk or one or more limbs

Neuropathic pain

Absent abdominal reflex

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12
Q

Diagnosis criteria for MS is called

A

Mc donald criteria

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13
Q

What is diagnostic criteria of MS based on

A
  1. How many attacks (0 - 2 or more)
  2. How many lesions (0 - 2 or more)
  3. Additional criteria (needed when attacks and lesions are low in number. based on dissemination on MR)
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14
Q

Diagnostic tools in MS

A
  • MR
  • CSF examination
  • Evoked potentials
  • Serology (ddx.)
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15
Q

Treatment of MS

A
  • Acute attacks = high dose glucocorticoids + plasmapheresis
  • Autologous stem cell transplant
  • Disease-modifying drugs (slow progression); interferon beta, glatiramer acetate, teriflunomide
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16
Q

Characteristics of MS progression

A

Most people with MS have a relapsing-remitting disease course. They experience periods of new symptoms or relapses that develop over days or weeks and usually improve partially or completely. These relapses are followed by quiet periods of disease remission that can last months or even years.