multiple sclerosis Flashcards
what is a MS
immune-mediated inflammatory, demyelinating, condition that affects both the brain and spinal cord
demyelination of the white matter of the CNS that tends to favour the optic nerves, brainstem, periventricular areas + spinal cord
demyelination decreases conduction velocity and some of the signal dissipates causing information to be lost
when does it start
MS is commoner in women than men and typically occurs in temporal regions. Symptoms typically commence in early life (20s and 30s) in the form of visual or sensory disturbances.
symptoms of MS
Visual
- optic neuritis: common presenting feature
optic atrophy, pale disc - Uhthoff’s phenomenon: worsening of vision following rise in body temperature
- internuclear ophthalmoplegia
Sensory
- paraesthesia - pins/needles
- numbness
- trigeminal neuralgia
- Lhermitte’s syndrome: paraesthesiae in limbs on neck flexion
Motor spastic weakness: most commonly seen in the legs - horners - bells - incontinence
Cerebellar
ataxia: more often seen during an acute relapse than as a presenting symptom
tremor worst on movement
Others
urinary incontinence
sexual dysfunction
intellectual deterioration
what is bulbar palsy
9, 10, 11, 12
Ix for MS
neurological examination
- Symptoms have to be progressive over a period of 1 year to diagnose primary progressive MS.
1. MRI of brain or spinal cord - will demonstrate demyelination plaques
2. Immunoelectrophoresis of CSF - will show oligoclonal bands of IgG
MRI - dorsum fingers
LP - elevated levels of IgG Oligoclonal bands
increase WBCs
3 main patterns of clinical presentation
- Relapsing remitting
- Secondary progressive
- Primary progressive
what is relapse remitting MS
they occur in different areas and different episodes
when you have attacks for at least 24 hours and then get better
what is secondary progressive
when you start off with remitting and then it gradually gets worse without relapses
what is primary progressive MS
it gets worse from the beginning
symptoms of optic neuritis
- Central scotoma. This is an enlarged blind spot.
- Pain on eye movement
- Impaired colour vision
- Relative afferent pupillary defect
McDonald criteria for MS
- Lesions consistent with an inflammatory process
- No alternative diagnosis
- Multiple lesions in time and space (Relapsing remitting MS)
- Progressive neurological deterioration for 1 year (Primary progressive MS)
how can a MS relpase be diagnosed
- Develops new symptoms
- Has rapid worsening of existing symptoms
- Symptoms last for more than 24 hours in the absence of infection or other cause after a stable period
of one month or more
treatment for MS relapse
500mg 5 days course of ORAL steroids
OR
IV of steroids in hospital
METHYLPREDNISOLONE
fatigue treatment for MS
amantadine
other options include mindfulness training and CBT
spasticity treatment for MS
baclofen or gabapentin
Other options include diazepam, dantrolene and tizanidine
physiotherapy is important