Multiple sclerosis Flashcards

1
Q

UMN or LMN?

A

UMN

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2
Q

Pathology?

A

Innate and adaptive immunity attacking oligodendrocytes
Demyelination and improper remyelination
Also some axonal damage

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3
Q

Character of the disease?

A

Relapsing and remitting

65% of R+R patients will go on to have secondary progressive MS

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4
Q

Symptoms of optic neuritis:

A

Reduced VA and colour vision
RAPD
Central scotoma (blind spot in centre of vision)
Papilloedema

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5
Q

What does internuclear ophthalmoplegia suggest?

A

In a young patient it is characteristic of MS

In an old patient it suggests stroke

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6
Q

What causes internuclear ophthalmoplegia?

A

Lesion of the medial longitudinal fasciculus

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7
Q

What is Lhermitte’s sign and what does it suggest?

A

Neck flexion sends pain down the back
MS in the young
Or B12 deficiency

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8
Q

What does MRI reveal in an MS patient?

A

Large ventricles
WM lesions around ventricles and more distal (dark lesions in T1)
Bright optic nerves from optic neuritis
Dorsan’s fingers - lesions coming out of ventricles + corpus callosum

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9
Q

What does lumbar puncture of an MS patient show?

A

Oligomeric bands

B cells

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10
Q

Diagnosis:

A

Show chronicity:
Multiple attacks
OR one attack with multiple lesions on MRI
OR one attack + oligomeric bands

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11
Q

Visual symptoms of MS:

A

Optic neuritis
Optic atrophy (pale disc)
Uhtoff’s: worse vision with raised body temperature
Internuclear opthalmoplegia

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12
Q

Cerebellar symptoms of MS:

A

Ataxia: acute relapse > presenting

Tremor

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13
Q

Motor symptoms of MS:

A

Spastic weakness most commonly in the legs

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14
Q

Sensory symptoms of MS:

A

Pins and needles feeling
Numbness
Trigeminal neuralgia
Lhermitte’s syndrome

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15
Q

What is primary progressive MS?

A

MS which has a later onset (40-50s)
Affects men and women equally
Constantly gets worse

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16
Q

What is secondary progressive MS?

A

Relapsing-remitting course but with neurological deterioration
Developed neurological signs and symptoms between relapses
Gait and bladder disorders

17
Q

Treatment of an acute relapse?

A

Only treat if causing distress/limiting activities
Exclude underlying worsening of symptoms - check urine
High dose steroids can be given 500mg for 5 days or 1g for 3 days to reduce length of relapse

18
Q

Disease modifying drugs:

A

Beta-interferon reduces relapse rate by 30%
Glatiramer acetate is an ‘immune decoy’
Natalizumab stops leukocytes crossing BBB
Fingolimod prevents lymphocytes leaving LNs
Other biologics

19
Q

Risk of drugs?

A

Wrong drug can kill - only give if at that stage of the disease

20
Q

Risk of treating MS?

A

Progressive multifocal leukoencephalopathy (PML)

Oppurtunistic viral infections in the brain

21
Q

What is NEDA?

A

No perceived relapses
No active T2 lesions
No active T1 Gd and lesions
No confirmed disability progression