Multiple Sclerosis Flashcards

1
Q

Pthological process of MS

A

demylination of neurones through repeated/persistant inflammation and may eventually result in the loss of the neurons

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2
Q

Age on onset for MS

A

Often 20-30

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3
Q

Things that might increase the chance of developing MS

A

Genetics, autoimmune disease, female (slightly) temparate climates (?), vitamin d (?), viruses eg Epsteinbarr (?)

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4
Q

What is the initial presentation of MS

A

Initially presents as some form of neuronal inability (demylenation of white matter in CNS), over a few days and stabilises within days/weeks, may or may not fully recover

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5
Q

What can relapses present as?

A

-Optic neuritis
-Sensory symptoms
-Limb weakness
-Brainstem (Diplopia, Vertigo/Ataxia)
- Spinal cord (bilateral motor and sensory symptoms/ Bladder involvement)

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6
Q

What is relative afferent pupillary defect and when would it present? What are the other signs of this?

A

It is when if you check the pupillayry reflex, then if you shine the light in the good eye, both eyes will constrict, if you shine the light in the bad eye, both eyes will dilate and then back to the good eye and both pupils will constrict again.

Can present as part of optic neuritis.

Other symptoms may include:
-Subacute visual loss
-Pain on moving eye
-Colour vision impaired

Will see optic disc swelling and later optic atrophy

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7
Q

What is internuclear opthalmoplegia?

A

When if you look right then left, one of the eyes won’t adduct. Present as part of a brainstem relapse

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8
Q

What can a spinal chord lesion present as?

A

Partial or Transverse (complete) Myelitis

-Sensory level often with band of hyperaesthesia
-Weakness/ upper motor neurone changes below level of demyelination
-Bladder and bowel involvement

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9
Q

What is the Demylenation due to?

A

Autoimmune, activated T cells crossing Blood brain barrier, inflammation and attack on myelin -> loss of function

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10
Q

What is glyosis and can this be seen on an mri scan?

A

Yes, present as white blobs (areas of inflammation) -> Glial cells (astrocytes) proliferation and scar tissue being laid down.

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11
Q

What are the needed for MS diagnosis?

A

At least 2 relapses in different areas of CNS - months or years apart

Posers criteria (purely clinical diagnosis)
MAcdonald Criteria (involves being able to see areas of inflammation or neuronal loss on MRI scan alongside the clinical symptoms)

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12
Q

What is clinically isolated syndrome?

A

No further episodes

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13
Q

What can induce relapses?

A

Being ill (infections)
3 months post-partum (although reduced chance during pregnancy)

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14
Q

What causes the progression and development of MS?

A

Axonal loss important in disease progression and development of persistent disability

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15
Q

What is dysesthsia?

A

Painful pins and needles

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16
Q

What are the signs and symptoms of the progressive phase in MS

A

MANY

Fatigue, temperature sensitivity
Dysesthesia/ paraesthesia
Stiffness or spasms
Balance, slurred speech
Bladder & bowel symptoms
Diplopia/ oscillopsia/ visual loss
Swallowing problems
Cognitive-memory/ emotional lability

17
Q

What may thesigns of MS be on examination? What does it depend on?

A

Afferent pupillary defect
Nystagmus or abnormal eye movements
Cerebellar signs
Sensory signs
Weakness
Spasticity
Hyperreflexia
Plantars extensor

18
Q

What are the types of MS

A

Relapsing remitting-85% at outset (RRMS)
Secondary progressive (SPMS)
Primary progressive – 10-15% (PPMS)

19
Q

What is different in Pirmary progressive MS

A

Often older onset and worse prognosis

20
Q

Wha tyis the Macdonald Critria reliant on?

A

Evidence of change on MRI

21
Q

What does a white blob mean on an MrRI

A

Inflammation

22
Q

What does gadolinium heltp to show up?

A

ACTIVE infkammation

23
Q

Lumbar puncture of MS results

A

Mainly normal, except present oligoclonal bands in CSF but not in the serum.

“Normal CSF glucose and protein
Few if any white cell count
oligoclonal bands present in CSF but not serum”

24
Q

Other investigations can be done?

A

Visual/ somatosensory evoked response
Relevant blood tests e.g.serology, autoantibody screen
Chest X Ray

25
Q

What are differential diagnoses?

A

Depends on symptoms and signs and on whether a first relapse or progressive disease
Includes:
Acute Disseminated Encephalomyelitis (ADEM)
Other causes demyelination (NMO etc)
Other Auto-immune conditions eg SLE
Sarcoidosis
Vasculitis
Infection eg Lyme disease, HTLV-1
Adrenoleucodystrophy etc etc

26
Q

Differential diagnosis of optic neuristis?

A

Neuromyelitis optica
Sarcoidosis
Ischaemic optic neuropathy
Toxic/ drugs/ B12 deficiency
Wegeners granulomatosis
Local compression
Lebers hereditary optic neuropathy
Infection-TB, HIV

27
Q

Myelitis differential diagnosises

A

Inflammation
(Neuromyelitis optica, SLE, sarcoidosis)
Infection…or post infection
(HIV, HTLV-1, HSV, TB, borrelia, mycoplasma etc)
Tumour
Paraneoplastic process
Stroke

28
Q

If presenting with acute replase, look for what?

A

UNDERLYING INFECTION

29
Q

ACUTe relapse treatment

A

Oral prednisolone and symptom treatment

30
Q

1st and second line treatment to stop rela[ses

A

Mainly all immunomodulators!!!

s/c or i/m injections
Beta-interferons
glatiramer acetate

OR

Oral treatments - worse side effects
Teriflunomide
Dimethyl Fumarate (immunosupressant)

SECOND LINE: (immunomodulators)
Natalizumab
Fingolimod
Cladribine
Ocrelizumab (?PPMS)

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