CNS Flashcards

1
Q

What is Parkinsonism?

A

Movement disorder of bradykinesia plus rigidity/tremor/postural instability

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2
Q

What are the causes of Parkinsonism?

A

Idiopathic - PD
Lewy Body Dementia
Dementia pugilistica
Normal pressure hydrocephalus
Parkinson plus syndromes - multiple system atrophy, progressive supranuclear palsy, corticobasal degeneration
Drugs - chlorpromazine, metoclopramide, prochlorperazine, sodium valproate, methyldopa
Wilson’s disease

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2
Q

Features of multiple systems atrophy

A

Parkinsonism
Autonomic failure
Cerebellum dysfunction
Pyramidal signs

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3
Q

What is a Lewy body?

In what diseases are they found?

A

Cytoplasmic inclusion protein of alpha synuclein

Lewy body dementia
Parkinson’s disease
Alzheimer’s

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4
Q

Features of progressive supranuclear palsy

A

Most common Parkinson plus syndrome
Supranuclear gaze palsy - abnormal vertical then horizontal saccades
Difficulty opening eyes
Significant problems with falls

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5
Q

Causes of a unilateral ptosis

A

3rd nerve palsy
Horner’s syndrome
Myasthenia gravis
Congenital

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6
Q

Causes of bilateral ptosis

A

Myasthenia gravis
Tabes dorsalis (dorsal column demyelination from syphilis)
Myotonic dystrophy
Syringomyelia causing b/l horner’s
Miller fisher syn (GBS and ocular paralysis)
Nuclear 3rd nerve palsy

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7
Q

Symptoms and Causes of a central Horner’s syndrome (1st order neurone)

A

Ptosis, miosis and anhidrosis of face/arm/upper trunk

Demyelination
Brainstorm or cord tumour/haemorrhage/infarct
Neck trauma
Syringomyelia 
Basal meningitis
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8
Q

What are the structures of the cavernous sinus?

A

CNs: 3, 4, 6, V(1 and 2)
internal carotid a
sympathetic carotid plexus

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9
Q

Features of a cavernous sinus lesion

A

unilateral CN palsies (3 4 and 6)
decreased sensation in V1 (ophthalmic) and V2 (maxillary)
loss of corneal reflex (V1)
proptosis (if pulsatile suggests carotico-cavernous fistula)
visual loss
papilloedema

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10
Q

Causes of an upward gaze palsy?

A
progressive supranuclear palsy
Graves ophthalmopathy
Myasthenia Gravis
Miller Fisher syndrome
Muscular dystrophy
Parinaud syndrome
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11
Q

What is the pathophysiology of Myasthenia Gravis

A

autoimmune destruction of nicotinic acetylcholine receptors on the post-synaptic membrane.
80-90% have anti-AChr antibody

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12
Q

DDx for bilateral ptosis and facial weakness

A

Miller Fisher syndrome
botulism
lambert-eaton myasthenic syndrome LEMS (paraneoplastic anti voltage gated calcium channels, from small cell lung ca)

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14
Q

DDx for bitemporal hemianopia

A

optic chiasm lesion
pituitary adenoma (upper vision affected 1st)
craniopharyngioma (lower vision affected 1st)
suprasellar meningioma
glioma
granuloma
metastases

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15
Q

features of myotonic dystrophy

A
wasting and weakness of hands
myotonia (grip hands then let go)
DM (dip urine)
catatarcts
distal areflexia
ptosis
dysarthria and dysphagia (ask about swallowing)
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16
Q

investigations for ?MS

A

CSF - oligoclonal IgG bands
MRI - periventricular white matter plaques
Visual evoked potentials - delayed velocity but normal amplitude

17
Q

Mx of MS

A

interferon-beta and glatiramer - decrease relapse rate but don’t slow progression
monoclonal antibodies eg rituximab
methyl-pred during relapses
baclofen
laxatives and intermittent self catheterisation

18
Q

Causes of spastic legs

A

inflam - MS
trauma
MND
syringomyelia
spinal cord compression/cervical myelopathy
Friedreich’s ataxia
subacute combined degeneration of the cord