Multiple sclerosis
Autoimmune CNS demyelination (disseminated in time and space)
Overview
A chronic autoimmune demyelinating disease of the CNS, defined by neurological episodes DISSEMINATED IN TIME AND SPACE. Typically a young woman with relapsing-remitting attacks (optic neuritis, sensory, motor, cerebellar). Diagnosis combines clinical episodes, MRI lesions and CSF oligoclonal bands.
Recognise
- Optic neuritis (painful monocular visual loss, RAPD), internuclear ophthalmoplegia
- Sensory (numbness, Lhermitte sign), motor/spasticity, cerebellar (ataxia, tremor), bladder dysfunction
- Uhthoff phenomenon (worse with heat); relapsing-remitting (85%) → secondary progressive
Red flags
- Acute relapse with disabling features; progressive course; tumefactive/atypical presentations
Differentials & how to tell them apart
Investigations
MRI brain + cord (periventricular/juxtacortical/infratentorial/cord lesions — disseminated in space and time); CSF oligoclonal bands; visual evoked potentials; exclude mimics (NMO/AQP4, B12).
Management
Acute relapse: high-dose methylprednisolone; long-term: disease-modifying therapy
- 1Acute relapse → high-dose methylprednisolone (shortens the relapse, does not alter the degree of eventual recovery).Gate: Steroids treat the relapse but do NOT modify the disease course — long-term relapse reduction needs a disease-modifying therapy, prescribed by neurology
- 2Disease-modifying therapy for relapsing-remitting MS; symptomatic management of spasticity, bladder, fatigue, neuropathic pain; MDT rehab.
Key points
Disseminated in time AND space is the definition. Optic neuritis + internuclear ophthalmoplegia + Lhermitte/Uhthoff in a young woman is the classic picture. Steroids for relapse ≠ disease modification.
Monitor & prognosis
Relapse frequency, MRI lesion burden, disability, DMT safety.
Variable; worse with motor/cerebellar onset and high lesion load.
Source: NICE NG220 (multiple sclerosis)