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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
- spasticity
- urge incontinence
- recent relapse
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
- cerebellar dysarthria
- Cranial Nerves
Limbs
- spasticity
- clonus
- pyramidal weakness
- reflexes very brisk
- finger flexion jerks
- Hoffman's sign
- absent abdominal reflexes
- bilateral extensor plantars
- sensory disturbance
- finger-nose ataxia
- gait
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
- smoothly rounded contours
- usually in white matter or occasionally across grey/white junction
- preference for
- optic nerves
- optic chiasm
- corona radiata
- brainstem
- periventricular areas
- spinal cord
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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