Demyelination- MS Flashcards

1
Q

what is MS?

A

a chronic and progressive condition characterised by demyelination of neurons in CNS, where lesions are seen disseminated in time and space

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2
Q

Pathophysiology?

A

thought to be caused by an inflammatory process involving immune destruction of myelin sheath

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3
Q

Epidemiology?

A
  • females > males
  • aged 20-40
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4
Q

Aetiolgy?

A
  • genes
  • EBV
  • smoking
  • obesity
  • Vit D deficiency
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5
Q

Presentation?

A
  • Optic Neuritis - most common presentation
  • Cr.N 6 involvement
    • diploplia
    • interneuclear opthalmoplegia
    • conjugate lateral gaze disorder
  • focal weakness
  • focal sensory weakness
  • ataxia
    • sensory
    • cerebellar
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6
Q

What is optic neuritis and what are the key features? mnemonic

A

Unilateral reduced vision due to demyelination in the optic nerve, presents over hours to days

features:

  • Pale disc/ Pain on eye movement
  • Loss of visual acuity / Loss of colour vision (red)
  • Afferent pupillary defect
  • Central scotoma - enlarged blind spot
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7
Q

what should be done in acute loss of vision?

A

referred urgently to opthalmologist, should be treated w steroids. Takes 2-6 weeks to recover

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8
Q

What are some presentations of focal weakness?

A
  • bell’s palsy
  • Horner’s syndrome
  • limb paralysis
  • incontinence
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9
Q

What are some presentations of focal sensory weakness?

A
  • trigeminal neuralgia
  • numbness
  • paraesthesiae
  • Lhermitte’s sign
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10
Q

What is Lhermitte’s sign?

A

Electrical shock sensation travelling down spine and to limbs upon forward flexion of neck. Indicates disease in cervical spine.

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11
Q

What is ataxia?

A

Problem with co-ordinated movement.

(many symptoms mimic those of being drunk- slurred speech, loss of coordination, stumbling, falling)

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12
Q

What is the issue in sensory ataxia? Test ?

A

Loss of proprioceptive sense.

  • positive Romburg’s test
  • can cause pseudoathetosis
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13
Q

Disease pattern?

A
  • Clinically isolated syndrome
    • can never happen again or progress to MS. If lesions are spotted on MRI, v likely it will progress to MS.
  • Relapsing-Remitting
    • most common pattern at initial diagnosis.
  • Secondary progressive
    • after initially presenting as relapsing-remitting, symptoms gradually worsen with incomplete remission. Symptoms become more and more permanent.
  • Primary progressive
    • symptoms gradually worsen from initial diagnosis with no relapsing-remitting course
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14
Q

Diagnosis?

A

clinical diagnosis- based on symptoms and clinical picture

Ix:

  • MRI- demyelinating lesions
  • LP- oligoclonal bands in CSF
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15
Q

how long do symptoms have to be present for to diagnose primary progressive MS?

A

symptoms have to be progressive for at least 1 year

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16
Q

Mx?

A
  • disease modifying drugs / biologics
  • Treating relapses:

Acute flare –> Methylprednisolone

  • 500mg orally daily for 5 days
  • 1g IV daily for 3-5 days where oral not worked before/severe relapse

Symptomatic

  • Depression–> SSRI
  • Urge incontinence–> Anticholinergics
  • Spasticity–> antispasmodic ie Baclofen
  • Neuropathic pain–> gabapentin/amitriptyline