Clinical diagnosis: two neurological events separated in time and neurological location
Prevalence
- Increases moving north from the Equator
- 60-100/100000 in the UK
Aetiology
- Increased concordance among monozygotic twins
- HLA haplotype A3, B7, D2 and DR2 is more common
Environmental
- ?Viral infection
- ?Dietary antigens
Pathology
- Plaques of demyelination particularly in
- Optic nerves
- Periventricular region
- Brainstem and cerebellar connections
- Cervical spinal cord
- Corticospinal tracts
- Posterior columns
Clinical patterns
- Relapsing/remitting
- Chronic progressive
Investigation
- Imaging
- MRI brain and spinal cord (visualises multiple plaques)
- CSF
- Oligoclonal bands in 80%
- Raised mononuclear cell count 5-60 cells/mm^3
- Visual evoked responses
- Delayed following optic neuropathy
Management
- No treatment has been shown to alter long-term outcome
- Corticosteroids - I.V. methylprednisolone or ACTH may speed recovery in acute relapses
- Beta-interferon - reduces relapse rate but not long-term outcome
- Physiotherapy
- Occupational therapy
- Walking aids
- Wheelchairs
- Car/house conversions
- Speech therapy
- Counselling
Prognosis
- Unpredictable course ranging from grave disability to mind and benign
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