Multiple Sclerosis Flashcards
Features of MS
Auto-immune inflammatory disease
Affects the CNS
Relapsing and remitting –> progressive
Demyelination and axonal degeneration
Features of transverse myelitis
Inflammatory demyelination of the spinal cord
Subacute non-compressive myelopathy
Symptoms over hours to days –> improvement over weeks to months
Causes:
- Infection - CMV, EBV, Mycoplasma, HTLV, HIV
- MS
- Idiopathic
Features of optic neuritis
Presenting symptom of MS in 20-50%
Acute or subacute unilateral eye pain
Variable degree of visual loss
Colour desaturation
RAPD or marcus gunn pupil
Improves over weeks -months
Risk of progression to MS by MRI - T2 lesions
Diagnosis of optic neuritis?
Visual provoked responses
CSF for the diagnosis of MS?
Evidence of Intra thecal immunoglobulin synthesis
Only in CSF not serum
Adds prognostic value for the development of MS after a single attack
What is L’Hermitte’s sign?
Shock like sensation when neck is flexed
What is Uhtoff’s phenomenon?
Reversible and stereotypic decrements in physical and cognitive function due to increased body temperature
Nerve conduction slowing due to increased core temp
After a single demylinating event who gets MS?
Predicted by number of T2 lesions on MRI
Presence of oligoclonal bands on CSF increases risk
Why treat MS early?
Physical and cognitive outcomes are determined early in the disease = Benign MS is not benign
Early treatment reduces lesions and disease burden
Diagnosing MS on MRI?
Dissemination of lesions in time and space
Dissemination in space:
Lesions in 2 or more areas of CNS - periventricular, juxtacortical, infratentorial, spinal cord
Dissemination in time:
New lesion on follow up imaging OR simultaneous non-enhancing and enhancing lesions
Cerebral atrophy
T1 hypointense - black lesions of permanent axonal loss
What is devic’s disease?
Relapsong-remitting involvement of the optic nerves and spinal cord
MRI = long lesions without brain involvement
Anti-aquaporin 4 antibodies
Anti-MOG antibodies
What is acute disseminated encephalomyelitis?
Infectious prodrome 1-4weeks prior
–> encephalopathy with behavioural changes
Most recover
PML V.s. MS
Reactivation of the JC virus
–> progressive demyelinating and fatal infection of the brain
Subacute onset
Progressive over weeks
Behavioural and neuropsychological alteration
MRI = Large >3 lesions, subcortical T2 lesions
JCV PCR of CSF is diagnostic
Treatment of PML
Stop immunosuppression
Consder immune reconstitution but risk of IRIS
Aetiology of MS
Genetics:
- Family history
- HLA-DR2
F>M
Latitude gradient -? role of vitamin D
Smoking
EBV