Multiple Sclerosis (MS)
Multiple Sclerosis (MS) is a chronic, progressive condition characterised by plaques of demyelination and eventual axonal loss in the CNS. It typically presents in women around 20-50 yrs. The main 2 charasteristics of it are:
Clinical attack of MS e.g. optic neuritis
Disseminated in Time and Space
Time - neurological damage occurring at multiple points in time
Space - damage affecting multiple areas of the CNS
Classification
Relapsing-Remitting (80%)
Primary Progressive - disease gets worse from beginning
Secondary Progressive - disease starts off as relapsing-remitting before becoming progressively worse
N.B. Myelin cells are called Oligodendrocytes in the CNS, and Schwann cells in the PNS.
Presentation
Common presenting features are:
Optic Neuritis - blurred vision, painful eye movements, and colour blindness (esp. red)
Patchy parasthaesia - sensory disease
Other features include:
Internuclear ophthalmoplegia - lesion in MLF (medial longitudinal fasciculus) of the brainstem
Impaired adduction ipsilateral to the lesion
Nystagmus contralateral to the lesion
Ataxia - sensory or cerebellar
Spastic paraparesis
N.B. MS is a CNS disease, so the pt shouldn’t present with any LMN signs!
Investigations
History and examination
Bloods - FBC (WCC), CRP
MRI Brain + Spine w/Contrast - typically see periventricular white matter lesions
A plain MRI would be used to look for evidence of demyelination, whilst the contrast (gadolinium) enhances some lesions and not others to demonstrate dissemination in space.
LP - presence of CSF Oligoclonal bands, which indicates an autoimmune process in the CNS
N.B. Important to rule out infection before treating.
Management
Acute attack - Methylprednisolone 1g IV
Long-term:
Disease-modifying therapies e.g. Beta-interferon
Baclofen and botox for spasticity
Anticholingerics (e.g. Oxybutynin) for bladder incontinence
Gabapentin/Pregabalin for neuropathic pain
N.B. Intermittent self-catherisation can be an option in those with a neuropathoic bladder.