Multiple Sclerosis

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Multiple Sclerosis


  • neurological symptoms separated in time and focus
  • disease characterised by focal plaques of Demyelination
  • often a young patient
  • slightly more common in women
  • prevalence 1:1000

Presentation

  • usually between 20-40
  • reason for present admission e.g.
    • difficulty walking
    • loss of balance 
    • double vision
    • bladder symptoms
    • respite

History

  • when / how first presented
  • course of illness to date
    • Relapsing / Remitting
      • number / frequency of episodes
      • nature of relapses
    • secondary progressive
    • Chronic progressive
    • progressive relapsing
  • level of disability in 'steady state'
  • bladder symptoms
  • Uhthoff's phenomenon
  • Lhermitte's sign
  • impotence
  • fatigue

FHx

  • no clear cut pattern of inheritance
    • 5-15 x risk if first degree relative

DHx

ROS

SHx

  • able to work
  • invalidity benefit
  • other allowances
  • ambulant
  • wheelchair
  • able to transfer
  • carer
  • district nurse
  • home help

Examination

General

  • depressed / euphoric / anxious

CNS

Limbs

  • spasticity 
    • legs > arms
  • clonus
  • pyramidal weakness
    • legs > arms
  • reflexes very brisk
    • finger flexion jerks
    • Hoffman's sign 
  • absent abdominal reflexes
  • bilateral extensor plantars
  • sensory disturbance
    • patchy
  • finger-nose ataxia
  • gait 
    • spastic
    • ataxic

Investigations

  • visual evoked responses
    • delayed=slow conduction in white matter
  • CSF
    • slight increase in mononuclear cells (30%)
    • slight increase in protein (40%)
    • oligoclonal bands (90%)
  • MRI
    • high signal lesions esp. periventricular

Pathology

Macroscopic

  • plaques of variable size
    • usually <2cm
  • smoothly rounded contours
  • usually in white matter or occasionally across grey/white junction
  • preference for

Microscopic

  • loss of myelin
  • axons preserved
  • a few lymphocytes cluster around small vessels
  • influx of macrophages
  • considerable oedema
  • demyelination is total within plaques
  • neuronal bodies spared
  • ageing plaques acquire astrocytes and glial processes → impaired structural integrity of axons

Course

  • relapses with complete recovery between
  • frequent relapses
  • relapses with incomplete recovery
    • +/- change to chronic progressive
  • chronic progressive

Treatment

  • Acute relapse
    • IV steroids improve rate of recovery 
  • Interferons may work

Prognosis

  • favourable outcome if
    • onset of sensory symptoms
    • optic neuritis (if young)
  • adverse outcomes
    • progressive course
    • incomplete recovery from initial attack
    • cerebellar ataxia
    • persistent weakness
  • 20-30 years
    • death from respiratory paralysis or UTI
 

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