Multiple sclerosis Flashcards

1
Q

Define multiple sclerosis?

A

Inflammatory demyelinating disease of the CNS – discrete plaques of demyelination occur at multiple CNS sites, from T-cell mediated immune response

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2
Q

summarise the epidemiology of multiple sclerosis?

A

UK prevalence: 1/1000

2 x as common in FEMALES

Age of presentation: 20-40 yrs

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3
Q

what are the 4 types of multiple sclerosis?

A

Relapsing-Remitting MS

  • COMMONEST form
  • Clinical attacks of demyelination with poor healing in between attacks

Clinically Isolated Syndrome

  • Single clinical attack of demyelination
  • The attack in itself does NOT count as MS
  • 10-50% progress to develop MS

Primary Progressive MS

  • Steady accumulation of disability with NO relapsing-remitting pattern

Marburg Variant

  • Severe fulminant variant of MS leading to advanced disability or death within weeks
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4
Q

what are the risk factors for MS?

A

Females

EBV exposure

Prenatal vitamin D levels

Smoking

Other AIs

IL7RA and IL2RA associated with increased risk of MS

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5
Q

describe the aetiology of MS

A

UNKNOWN

Autoimmune basis with potential environmental trigger in genetically susceptible individual

Immune-mediated damage to myelin sheaths results in impaired axonal conduction

Deposition of beta amyloid plaques and tau protein fibres tangles

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6
Q

what is uhtoff’s sign?

A

worsening of neurological symptoms as the body gets overheated from hot weather, exercise, saunas, hot tubs etc.

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7
Q

what is Lhermitte’s/ Barber seat Sign?

A

an electrical sensation that runs down the back and into the limbs when the neck is flexed

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8
Q

what are the signs of MS on physical examination?

A

Optic Neuritis

  • Impaired visual acuity (MOST COMMON)
  • Loss of coloured vision

Visual Field Testing

  • Central scotoma (if optic nerve is affected)
  • Scotoma = a blind spot in the normal visual field
  • Field defects (if optic radiations are affected)

Relative Afferent Pupillary Defect (RAPD)

Internuclear Ophthalmoplegia

  • Lateral horizontal gaze causes failure of adduction of the contralateral eye
  • Indicates lesion of the contralateral medial longitudinal fasciculus

Sensory

  • Paraesthesia

Motor

  • UMN signs

Cerebellar

  • Limb ataxia (intention tremor, past-pointing, dysmetria)
  • Dysdiadochokinesia
  • Ataxic wide-based gait
  • Scanning speech
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9
Q

what is the typical presentation of MS?

A

Different neuro symp (optic neuritis - painful blurred vis - is common) sep by time and oligoclonal bands in CSF which aint in serum

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10
Q

what gives a better prognosis of MS?

A
  • Onset under 25 yrs
  • Optic neuritis or sensory symp at first presentation
  • Long interval between relapses (>1yr)
  • Few lesions on MRI
  • Full recovery from previous relapses
  • Female
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11
Q

What are the presenting symptoms of MS?

A
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12
Q

What criteria is the diagnosis of MS based on?

A

Diagnosis is based on the finding of two or more CNS lesions with corresponding symptoms,separated in time andspace- McDONALD CRITERIA

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13
Q

what are the investigations for MS?

A

MRI Brain, Cervical and Thoracic Spine (with gadolinium) – shows lesions – some are active and some are older

Do a FBC and blood test to see if met, TSH and vitB is all norm

Lumbar Puncture

  • Microscopy - exclude infection/inflammatory causes
  • CSF electrophoresis shows unmatched oligoclonal bands – basically present in the CSF and not in the serum
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14
Q

What does CSF electrophoresis show in MS?

A

unmatched oligoclonal bands – basically present in the CSF and not in the serum

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15
Q

what does the MRI brain, cervical and thoracic spine with gadolinium show?

A

shows lesions – some are active and some are older

Plaques can be identified

Gadolinium enhancement shows active lesions (but not all lesions are enhanced with Gadolinium for a diagnosis of MS)

dissemination in time requires demonstration of new lesions compared to previous imaging.

During an acute attack, inflammation makes the blood brain barrier leaky-> allows immune cells into the CNS (normally brain is immune privileged). The GAD contrast as it will also cross the barrier during periods of acute inflammation.

This lights up any active lesions, and old lesions remain darker, so can see what’s old and what is new.

After an acute attack the blood brain barrier is leaky for around 2 to 6 weeks, so anything that lights up is at most 6 weeks old.

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