Multiple Sclerosis Flashcards

1
Q

Is MS more common in males or females?

A

Females

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2
Q

MS is a disease of

A

the white matter of the CNS which causes demyelination and relapsing, remitting disease

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3
Q

Factors of pathogenesis of MS

A

Complex genetic inheritance
Association with autoimmune disease
More common in temperate climates
Possible relationship to viruses and vitamin D exposure

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4
Q

Initial presentation of MS

A

80% present with a relapse - attack of demyelination or inflammation
Gradual onset over days
Stabilises over days/weeks
Gradual resolution to complete or partial recovery

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5
Q

Symptoms of relapse of MS

A
Optic neuritis 
Sensory symptoms 
Limb weakness 
Diplopia/vertigo/ataxia 
Bilateral symptoms and signs of spinal cord pathology 
Bladder and bowel symptoms
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6
Q

Presentation of optic/retrobulbar neuritis

A

Subacute vision loss in one eye
Pain on moving eye
Colour vision disturbed/desaturated

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7
Q

Process of optic neuritis

A

Initial swelling of optic disc followed by optic atrophy

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8
Q

Affect of optic neuritis on pupillary reflex

A

Relative afferent pupillary defect - dilation rather than constriction when light shone on pupil

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9
Q

Possible differential diagnoses for optic neuritis

A
Neuromyelitis optica 
Sarcoidosis 
Ischaemic optic neuropathy 
Toxin/drugs/B12 deficiency 
Wegners granulomatosis 
Local compression 
Leber's hereditary optic neuropathy
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10
Q

Presentation of brainstem relapse

A
Cranial nerve invovlement 
Internuclear opthalmoplegia 
Diplopia 
Vertigo 
Nystagmus 
Ataxia 
Upper motor neurone changes in limbs
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11
Q

Presentation of myelitis

A

Numbness/pins and needles in legs
Weakness/upper motor neurone changes below the level of numbness/pins and needle
Bladder and bowel invovlement
Increased reflexes

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12
Q

Presentation of further relapses of MS

A
May occur within months or years of first relapse 
Variable site and severity 
Optic nerve involvement 
Sensory involvement 
Limb weakness 
Diplopia 
Vertigo 
Ataxia 
Sphincter disturbance
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13
Q

Describe process of demyelination

A

Autoimmune process
Activated T cells cross blood-brain barrier and cause demyelination
Demyelination can repair, full recovery if normal repair, or scarring and gliosis if not completely repaired

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14
Q

How does demyelination appear on MRI?

A

As lesions or plaques

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15
Q

Describe the progression of demyelination in MS

A

Axonal loss - may be important in progression and development of disability
Black holes appear on MRI, later seen as cerebral atrophy

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16
Q

Presentation of progressive phase of MS

A
Accumulation of symptoms and signs 
Fatigue, temperature sensitivity 
Sensory involvement 
Stiffness/spasms
Poor balance 
Slurred speech 
Difficulty swallowing 
Diplopia, oscillopsia, visual loss 
Cognitive - dementia, emotional liability
17
Q

Most patients who present with relapsing remitting MS will go on to develop

A

secondary progressive disease

18
Q

Possible examination findings in MS (depends on location of demyelination and stage of disease)

A
Afferent pupillary defect 
Nystagmus/abnormal eye movements 
Cerebellar signs 
Sensory signs 
Weakness 
Spasticity 
Hyperreflexia 
Plantar extensor reflex
19
Q

How is MS diagnosed?

A

Based on clinical presentation, MRI and evidence of demyelination separated in time and space

20
Q

Investigations that should be done in suspected MS with an atypical clinical picture or MRI

A

Lumbar puncture
Visual/somatosensory evoked response
Bloods to exclude other inflammatory conditions
CXR

21
Q

Differential diagnoses for suspected MS with atypical presentation

A
Acute disseminated encephalomyelitis 
Other autoimmune conditions e.g. SLE 
Sarcoidosis 
Vasculitis 
Infection e.g. Lyme disease 
Adrenoleukodystrophy
22
Q

Type of MS

A
Relapsing remitting 
Secondary progressive 
Primary progressive 
Sensory 
Malignant
23
Q

First line agents for disease-modifying treatment of MS

A

Beta-interferons/glatiramer acetate daily/weekly IM/SC injection
Oral treatments - teriflunomide, dimethyl fumarate

24
Q

Possible side effects of first line agents for disease modifying treatment of MS

A

Flu-like symptoms
Injection site reaction
Abnormalities of blood count and liver function

25
Q

Second line agents for disease-modifying treatment of MS

A

Natalizumab
Fingolimod
Alemtuzumab

26
Q

Treatment of Progressive Multifocal Leukencephalopathy

A

Natalizumab, dimethyl fumarate or fingolimod
Annual MRI
JC virus antibody blood and urine 6-monthly

27
Q

Treatment of acute relapse of MS

A
Look for underlying infection 
Exclude worsening of usual symptoms with intercurrent illness 
Oral prednisolone 
Rehabilitation 
Symptomatic treatment
28
Q

Treatments for spasticity in MS

A

Muscle relaxants
Antispasmodics
Physiotherapy

29
Q

Treatments for dysaesthesia in MS

A

Amitriptyline

Gabapentin

30
Q

Treatments for urinary problems in MS

A

Anticholinergics
Bladder stimulation
Catheterisation

31
Q

Treatment for constipation in MS

A

Laxatives

32
Q

Treatment for vision problems/oscillopsia in MS

A

Carbamazepine

33
Q

Features of upper motor neurone lesion

A
Muscle weakness (pyramidal) 
Decreased control of active movement 
Spasticity 
Clasp-knife response 
Babinski sign 
Increased deep tendon reflex 
Pronator drift
34
Q

Features of lower motor neurone lesion

A
Muscle paresis/paralysis 
Fibrillation 
Fasciculations 
Hypotonia/atonia 
Hyporeflexia 
Strength not affected 
Muscle wasting (end stage)