neuro Flashcards

1
Q

what will a CT contrast imaging show of a basal subarachnoid haemorrhage

A

blood in the interhemispheric fissure and the sylvian fissure and all the sulci ventricles can be enlarged

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2
Q

what are the acute demyelinating polyneuropathies

A

Guillain-Barre syndrome

AIDS-seroconversion phase

lymphoma

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3
Q

pathological spreading is a sign of

A

UMN lesion

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4
Q

treatment of ischaemic stroke

A

alteplase

decompressive craniotomy

angiography - remove clot

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5
Q

why do you give vancomycin in the AB cocktail for meningitis

A

to try and gain some cover for high level resistant strains of strep pneumonia

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6
Q

what is claudication

A

ischaemic pain in exercising muscles - due to the imbalance between workload of muscles and the ability to maintain aerobic metabolism

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7
Q

how do you tell which eye is the dud one in diplopia

A

the one that moves the least = dud

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8
Q

lacunar infarcts affect which vessels

A

vessels to the basal ganglia, thalamus or deep white matter

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9
Q

differential diagnosis in someone with a new onset headache with cancer or IS

A

meningitis

brain abscess

metastasis

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10
Q

What is the term for worsening of sensory symptoms with heat?

A

Uhthoff’s phenomenon - relatively specific for MS

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11
Q

what is dystonia

A

abnormal muscle activity/tone leading to sustained postures and movements

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12
Q

treatment for ecephalitis

A

dexamethasone preceding ceftriaxone + vancomycin + penicillin (to cover for meningitis) + ACYCLOVIR

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13
Q

two common causes of acute vestibulopathy

A

vestibular neuronitis

brainstem/cerebellar stroke

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14
Q

what causes aneurysms (pathology)

A

weakness in elastin and collagen in the adventitia and media

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15
Q

how do mass lesions/tumours in the brain cause headache

A
  • traction on large blood vessels and dura
  • direct pressure on pain-sensitive areas
  • elevated ICP from hydrocephalus, mass effect or haemorrhage into or around the tumour
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16
Q

3 most common triggers for seizures

A

alcohol

sleep deprivation

non-compliance from meds

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17
Q

symptoms of carpal tunnel

A

pain in the whole hand, tingling discomfort which is most prominent at night

patients tend to shake their hand for the pain

fingers feel like sausages

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18
Q

major diagnostic finding to diagnose myopathy

A

CK >1000

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19
Q

what is primary lateral sclerosis

A

similar to ALS but no LMN signs –> better prognosis

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20
Q

how do you diagnose myasthenia gravis

A
  • tensilon test with short acting ACh antagonist (edrophonium)
  • blood test for autoantibodies
  • ACh R, MuSK
  • CT chest (for thymoma)
  • EMG studies
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21
Q

when someone has an intention tremor.. what do you think

A

cerebellar lesion

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22
Q

what are the complications of subarachnoid haemorrhage

A

hydrocephalus –> increased ICP vasospasm –> infarction

hypernatraemia

seizures

neurogenic pulmonary oedema

MI

late complications = PE, pneumonia

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23
Q

what are the common features of raised ICP headache

A

worse in the mornings

better after vomiting

exacerbated by cough or straining

drowsiness

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24
Q

what are the clinical features of myasthenia gravis

A

no muscle wasting or fasiculations

proximal weakness > distal normal reflexes and sensation weakness increasing with repetitive exercise

early involvement of extraocular muscles and lid opening muscles

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25
Q

signs and Sx of optic neuritis

A

RAPD

Swelling of the optic disc

painful eye movements

decreased visual acuity

decreased red colour saturation

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26
Q

tests for cranial nerves III, IV and VI

A

H test

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27
Q

treatment for demyelinating polyneuropathy

A

intragam

plasma exchange

Steroids (CIDP only)

immunosuppression

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28
Q

signs of motor neuron disease

A

muscle wasting

fasiculations

LMN and UMN signs

generalised weakness

reflexes preserved unti late

plantars may be upgoing

no sensory loss

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29
Q

why do you give dexamethosone to patients with suspected meningitis prior to giving them ABs

A

to try and prevent 8th nerve damage

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30
Q

how can you tell the difference between peripheral and central nystagmus

A

peripheral - nystagmus doesnt direction change (beats away from affected ear), mixed horizontal and torsional nystagmus

central - nystagmus direction changes, any kind of nystagmus

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31
Q

what 3 inherited conditions can predispose you to getting a brain tumour

A

neurofibromatosis 1 and 2

Li Fraumeni syndrome (p53 loss –> glioma)

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32
Q

what is a positive Head impulse test

A

when you see the correctional movement of the eyes going back onto the target (catch up sarcade)

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33
Q

acute treatment of stroke before knowing whether ischaemic or haemorrhagic

A

NIL oral

IV fluids of Normal saline

aspirin

clexane 40mg

neurological examinations 2 hourly

inform relatives

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34
Q

what signs do PD patients get due to their rigidity

A

stooped posture

reduced arm swing

stiffness through ROM in a joint

  • cog wheeling or lead pipe
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35
Q

explain the 2 phases of nystagmus

A

slow phase - retinal slip

fast phase - re-fixate on target alternate between slow and fast phases

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36
Q

what are the 2 prognostic factors that make it more likely for a patient to progress to having MS from a single presentation

A
  • the number of inflammatory lesions of baseline MRI brain
  • the presence of oligoclonal bands in the CSF
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37
Q

symptoms of severe ischaemia of the lower limbs

A

pain

parasthesia

pale

coolness

pulseless

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38
Q

how can you tell the difference in presentation between vestibular neuronitis and brainstem stroke

A

vestibular neuronitis - can stand on their own, unidirectional nystagmus, may be suppressed by fixation, HIT positive

brainstem stroke - cannot stand on their own, head impulse test negative, direction change nystagmus

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39
Q

what is the characteristic sign of BPPV during a Hallpike

A

period of latency and then a torsional nystagmus, then passess

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40
Q

explain the gait of someone with PD

A
  • short, shuffling
  • reduced speed
  • narrow base
  • forward trunk flexion (stooping)
  • reduced arm swing
  • festination or freezing
  • difficulty turning/changing direction
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41
Q

characteristic histological sign for meningioma

A

meningioma “whorls”

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42
Q

what are the red flags for headache

A
  • first/worst headache
  • abrupt onset
  • change or progression of pre-existing headache pattern
  • abnormal findings on physical/neurological exam
  • new headache in patients aged >50
  • new headache in patients with cancer, IS, pregnancy
  • triggered by exertion, sexual activity, Valsalva
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43
Q

most common cause of encephalitis

A

HSV

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44
Q

secondary prevention of stroke

A

BP lowering

statins

antiplatelet

AF prevention

carotid revascularization

anticoagulation

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45
Q

what disorder/disease is associated with myasthenia gravis

A

thymic hyperplasia

thymoma

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46
Q

in which reflex is spreading normal

A

brachioradialis

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47
Q

risk factors for stroke

A

hypertension, AF, acute MI, ventricular aneurys, RHD, prosthetic valves, Diabetes, cigarette smoking, increased W:H, heavy alcohol intake, polycythaemia, hypercholesterolaemia

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48
Q

meningiomas are most common in which population

A

women middle age

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49
Q

difference between simple and complex seizures

A

simple - no effects on awareness

complex - affects awareness

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50
Q

two main DDx for headache + seizures

A

tumour

haemorrhage

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51
Q

main treatment for PD

A

Levodopa + carbidopa (peripheral decarboxylase inhibitor)

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52
Q

localisation of a tumour in a patient with dysphasia

A

dominant frontal or temporal lobes

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53
Q

what causes the meningism symptoms associated with sub arachnoid haemorrhage

A

due to blood in the subarachnoid space

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54
Q

what is the acute treatment of MS flare

A

1g IV methylprednisolone for 3-5 days

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55
Q

most common symptom of low grade glioma

A

seizures

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56
Q

which primary tumours commonly metastasise to the brain

A

lung, breast, melanoma, kidney, GI

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57
Q

causes of peripheral nystagmus

A

BPPV

vestibular neuronitis

Meniere’s disease

Trauma

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58
Q

What is it called when a focal seizure starts off and then spreads for eg. up the arm

A

Jacksonian March

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59
Q

treatment of myasthenia gravis

A

ACh antagonists

plasma exchange

IV immunoglobulin

immunosuppression - steroids, azathioprine thymectomy

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60
Q

principles of treatment of brain metastases

A
  • commence dexamethasone
  • reduction in ICP and oedema
  • surgery to remove the metastasis if solitary or the patient has a reasonable life expectancy (occasionally some are removed for palliation)
  • whole brain radiotherapy
  • for multiple mets
  • stereotactic radiotherapy
  • for 1-3 mets
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61
Q

what are the signs/symptoms associated with segmental radiculopathy

A

pain/paraesthesia in a dermatomal distribution

weakness of muscles innervated by the root –> may atrophy

May have diminished/absent reflexes

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62
Q

lacunar infarcts are associated with

A

hypertension!

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63
Q

differential diagnosis in someone with headache triggered by exertion/sexual activity/valsalva

A

aneurysm

chiari malformation

posterior fossa tumour

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64
Q

what causes spinal compressive syndrome

A

epidural abscess - extension from spinal discitis or bacterial

osteomyelitis - bacteriaemia with seeding to epidural space

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65
Q

treatment of raised ICP caused by subarachnoid haemorrhage

A

elevation of the head (encourages venous return)

diuresis to reduce cerebral oedema/ECF

hyperventilation - intubate and ventilate if necessary

sedate/paralysis

remove mass

drain hydrocephalus

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66
Q

what are the causes of transverse myelitis

A

MS (common)

infectious

autoimmune disorders

No aetiology

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67
Q

What is Tod’s paresis/palsy

A

after a focal seizure the part where the seizure started in may have paralysis/paresthesia for a while after the seizure

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68
Q

survival with a low grade glioma

A

years to decades - eventually will progress to a higher grade and death

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69
Q

what is an ataxic gait

A

gait with a broad base (10-15cm) - looks drunken

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70
Q

how much time must pass between presentations for MS to classify them as disseminated

A

at least 1 month

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71
Q

what are the 4 common disorders of neuromuscular junctions

A

post synaptic - myaesthenia gravis

pre synaptic - Lambert Eaton myasthenic syndrome

botulism

tick paralysis

72
Q

how to test for dysphasia

A

No ifs ands or buts

73
Q

what are the clinical patterns of generalised epilepsy

A

absence

myoclonus

tonic-clonic

74
Q

what is the histological feature typical of gliomas

A

necrotic region with tumour cells “pallisading” at margin

75
Q

most common cause of nerve root injury

A

herniated intervertebral disk

76
Q

what is dysmetria

A

overshooting (in finger-nose test)

77
Q

primary prevention of aneurysms

A

stop smoking

control of hypertension

78
Q

the level of sensory deficit tells you what about the level of injury

A

the lowest possible level of injury (could be anywhere higher than this)

79
Q

explain the pathology behind parkinson’s

A

reduction in dopaminergic neurons in the pars compacta of the substantia nigra –> reduction of dopamine in the striatum –> increased inhibition of cortical motor areas

80
Q

two causes of motion induced vertigo

A

uncompensated peripheral vestibular lesion (following vestibular neuronitis)

BPPV

81
Q

3 surgical options for claudication

A
  • angioplasty +/- stenting - best for short segments in proximal arteries
  • endarterectomy - for short segments
  • bypass- for longer blocks
82
Q

tests for cranial nerve II

A

pupil reflexes

visual fields

acuity

83
Q

what is ischaemic rest pain

A

perfusion is so poor that there is pain at rest in the most distal part of the limb - some relief from perfusion by gravity

84
Q

symptoms of radial nerve lesion

A

wrist drop and cant extend their fingers

sensory disturbances in the dorsal, lateral part of the hand

85
Q

which is more common in Australia - infarct or haemorrhage

A

infarct (80%)

86
Q

what is an intention tremor

A

when the tremor gets larger when closer to the object

87
Q

hallmarks Sx for: meningitis encephalitis SOL syndrome spinal compressive syndrome

A

meningitis = headache

encephalitis = altered conscious state

SOL syndrome = focal neurological problems

spinal compressive syndrome = agonizing back pain

88
Q

differential diagnosis for abrupt onset headache

A

Subarachnoid haemorrhage until proven otherwise

  • pituitary apoplexy
  • bleed into a mass or AVM
  • mass lesion (especially posterior fossa)
89
Q

principles of treatment of a meningioma

A
  • total surgical excision and obliteration of the dural attachment is the most effective treatment
  • Rx for small, residual recurrent or malignant tumours
90
Q

what is oscillopsia

A

sensation that the visual world is moving

91
Q

management of ALS

A

speech pathology - swallow and communication

NIV

mobility

aids

riluzole (glutamate antagonist)

92
Q

what is dyskinesia

A

reversible levodopa-induced motor complication - abnormal involuntary movements

93
Q

principles of treatment for an astrocytoma

A
  • commence dexamethasone
  • reduction of cerebral oedema and ICP
  • resection of as much of the tumour as safely possibly
  • adjuvant therapy
  • Rx and Cx
94
Q

how can you tell if someone has internuclear opthalmoplegia

A

when you do the horizontal part of the H test - eyes wont move together - failure of adduction of one eye (stops at midline) with the other eye having nystagmus

95
Q

system for grading power

A

0 = nothing

1 = visible twitch

2 = movement with gravity

3 = suboptimal movement against gravity

5 = normal movement against resistance

96
Q

in the hospital, what is the likely Tx given to someone with suspected meningitis

A

dexamethasone preceding ceftriaxone + vancomycin + penicillin -> then do CT -> LP

97
Q

how do you die of a stroke (if you were to die of the stroke and not pneumonia)

A

oedema –> brain swelling –> raised intracranial pressure –> brainstem herniation –> death

98
Q

explain the blood supply to the brain

A

via internal carotid arteries (70%) and vertebral arteries (30%) which anastomose at Circle of willis (base of brain)

99
Q

what is the difference in the effect on the 3rd nerve between an intracranial mass and diabtes

A

intracranial mass - affects dilatory fibres more = pupillary dilation

diabetic = affect motor fibres more = pupillary constriction

100
Q

pharmacological treatment of generalised seizures

A

first line = Sodium Valproate

  • benzos
  • lamotrigine
  • ethosuximide
  • ?phenytoin
101
Q

what are the 4 clinical stages of spinal compressive syndrome

A

nuchal pain –> nerve root pain –> weakness –> paralysis

102
Q

describe the headache associated with a subarachnoid haemorrhage

A

sudden, severe headache at the back of the head associated with nausea and vomiting and photophobia and neck pain

103
Q

proximal weakness suggests which DDx

A

myopathy

myasthenia gravis

104
Q

what causes myasthenia gravis

A

antibodies that cross react with the ACh receptor as the neuromuscular junction

105
Q

How do you test cranial nerve V

A
  • Mastication/bite down on own teeth and feel masseter bulk
  • Corneal reflex (also tests VII)
  • check sensation in the 3 areas
  • ask to open their mouth
  • if weakness the jaw will move across
  • jaw jerk = absent is normal
106
Q

What do you think of with vertigo that lasts hours

A

migraine

Meniere’s disease

107
Q

goals of management for a subarachnoid haemorrhage

A

prevent rebleed - secure the aneurysm prevent complications pain relief

108
Q

types of delirium

A

hyperactive

hypoactive

mixed

109
Q

What do you think of with vertigo that lasts seconds

A

BPPV

uncompensated peripheral lesion

110
Q

how do you test for cranial nerve XI

A
  • ask to shrug shoulders and leave them up and then try to push them down (upper trapezius)
  • ask to get them to turn their head (opposite SCM to the way the head is turning)
111
Q

what is the most common type brain tumour

A

glioma (52%) - of these astrocytoma is the most common 44%

112
Q

what is the clinical sign of brainstem herniation

A

fixed dilated pupil (3rd nerve palsy (squished against cerebellar peduncle))

113
Q

what is an aneurysm

A

a focal dilatation of the artery

114
Q

management of spinal compressive syndrome

A

MRI ASAP –> neurosurgery or AB alone is neurosurgeons say so

115
Q

when you see multiple cerebral infarcts.. what should you think

A

watershed infarcts, emboli or vasculitis

116
Q

metabolic causes of secondary headache

A

OSA

present upon awakening

thyroid disease

B12 deficiency

exposure to CO and other toxins

hepatitis, renal disease, anaemia

117
Q

what inflammatory causes can cause myopathy

A

polymyositis

dermatomyositis

includion body myositis

118
Q

what is transverse myelitis

A

inflammatory demyelination of segment/s of spinal cord

119
Q

why do you give penicillin in the AB cocktail for menigitis

A

to treat for Listeria

120
Q

common levels of cervical stenosis

A

C5-6

C6-7

121
Q

What is Brown-Sequard syndrome

A

hemisection of the spinal cord causing:

  • contralateral impairment of pain and temp
  • ipsilateral weakness and impairment of proprioception, vibraction and light touch
122
Q

where are watershed infarcts

A

at the edge of two vascular territories

123
Q

signs/symptoms for spinal cord injury

A

reduced reflexes

weakness

paraesthesia

pain in the distribution of the nerve root

124
Q

what is a hemiplegic and diplegic gait

A

hemiplegic - circumduction with one leg (because foot is plantar flexed)

diplegic - cirumduction of both legs

125
Q

when is the peak incidence for gliomas

A

6-8th decade

126
Q

normal ICP

A

10-15mmHg

127
Q

what are the red flags associated with headache flagging sub-arachnoid haemorrhage

A

sudden onset

family history

hypertension

128
Q

when is the greatest risk of rebleed of a subarachnoid haemorrhage

A

first 24-48 hours

129
Q

how do you test for cranial nerve XII

A
  • muscle bulk
  • deviated tongue on protrusion (deviation will be towards the affected side)
130
Q

typical histological findings in polymyositis biopsy

A

inflammatory infiltrate around and INTO the muscle fibres

131
Q

what causes the raised ICP with a brain tumour

A

tumour mass surrounding oedema

hydrocephalus if CSF pathways are blocked

132
Q

most common form of motor neuron disease

A

amyotrophic lateral sclerosis

133
Q

how is nystagmus named

A

as per direction the quick phase

134
Q

typical bacterial meningitis LP

A

>1000 polymorphs, mostly leukcocytes protein >1g/L sugar decreased

135
Q

how do you test cranial nerve VII

A
  • corneal reflex (with V)
  • close your eyes tightly (orbicularis occuli) -> dont let me open your eyes (weakeness = opens)
  • smiling and bearing teeth
  • bear teeth and tighten neck muscles
136
Q

list the different ways an intracranial mass can present

A

Sx of raised ICP - headache, photophobia, drowsiness, confusion, seizures

focal neurological deficit

137
Q

safest seizure medication if pregnant

A

tegretol (carbamazepines)

138
Q

average life expectancy for ALS

A

if bulbar onset - 6-12 months

if limb onset - 2-5 years

139
Q

what is critical limb ischaemia

A

ischaemic rest pain with ulcers/gangrene and low trans-cutaneous oxygen pressure

140
Q

most dangerous seizure medication if pregnant

A

sodium valproate = Epilim (teratogenic)

141
Q

2 broad categories of seizures

A

generalized

focal/partial - often due to structural abnormalities

142
Q

what are the 4 primary symptoms of Gerstmann syndrome

A

dysgraphia/agraphia

dyscalculia/acalculia

finger agnosia

left-right disorientation

143
Q

prognosis for gliomas

A

7-14 months

144
Q

Treatment of Meniere’s disease

A

strict sodium restriction

diuretics

Surgery

145
Q

what do you see in a lumbar puncture for a subarachnoid haemorrhage

A
  • bloodstained CSF that does not clear on 3 consecutive collection tubes
  • xanthochromia (yellow staining due to breakdown of haemoglobin)
146
Q

what do you see in the CSF in someone with MS

A

oligoclonal bands (90%)

147
Q

common first presentations of MS

A

transverse myelitis

optic neuritis

brainstem/cerebellar presentations

148
Q

How do you diagnose MS

A

At least 2 clinical presentations disseminated in time and space, unattributable to other causes

149
Q

pharmacological treatment of partial seizures

A

carbamazepine

Sodium valproate

phenytoin

benzos

vigabatrin

lamotrigine

gabapentin

150
Q

definition of stroke

A

sudden cerebrovascular accident with abrupt onset of symptoms

151
Q

common presentation of a meningioma is symptomatic

A

raised ICP

focal neurological deficit

seizures

152
Q

What do you think of with vertigo that lasts days

A

vestibular neuronitis

stroke

153
Q

work up for an abrupt onset headache

A

neuroimaging

lumbar puncture

154
Q

what are the signs of anterior horn cell diseases

A

early muscle wasting

fasiculations

common diffuse weakness

reflexes normal or increased sensation normal

155
Q

which type of brain tumour can typically grow very large without symptoms

A

meningioma

156
Q

other treatments for PD

A

COMT inhibitors

MAO-I

Dopamine agonists

anticholinergics

amantadine

157
Q

what common drugs can cause myopathy

A

alcohol

statins

158
Q

two main bacterial causes of bacterial meningitis

A

N. meningitidis Strep pneumonia

159
Q

how do you test for cranial nerves IX and X

A
  • Gag reflex
  • look for normal movement of the soft palate
  • look for central uvula (deviation will be towards normal side)
160
Q

what causes dysarthria

A

impaired movement of the muscles required for speech

161
Q

severe/sudden ischaemia in the lower limbs is usually due to

A

embolus

162
Q

side effects of reperfusion of the lower limb in acute severe ischaemia

A

acute: shock
chronic: compartment syndrome

163
Q

how do you test balance

A

Romberg test - standing feet together and eyes closed standing on one foot and hopping

164
Q

symptoms of ulnar nerve lesion

A

wasting of pretty much all the small muscles of the hand

weakness and fasciculations

numb/tingling in medial 1.5 fingers

165
Q

Explain the look of an MS plaque on MRI

A

hyperintense lesion on T2 weighted MRI with active lesions showing enhancement with gadolinium

166
Q

Crossed sensory signs indicates

A

damage to spinal cord (on one half)

167
Q

cardiogenic embolism usually obstructs which cerebral artery

A

MCA

168
Q

4 main motor features of Parkinsons

A

rigidity

bradykinesia

pill rolling tremor

postural instability

169
Q

what sign is distinct for a headache caused by decreased ICP

A

headache relieved by lying down

170
Q

typical signs of claudication

A

pain on exertion

onset and severity related to workload

relieved with rest reproducible

171
Q

clinical presentation of cauda equina syndrome

A

acute lower back pain radiating to legs

bilateral sensory loss

saddle anaesthesia

172
Q

What is Meniere’s disease

A

Oedema of the inner ear

173
Q

which imaging would you order if you suspected subarachnoid haemorrhage

A

CT

174
Q

explain the principles of treatment of a low grade glioma

A
  • removal of as much as the tumour as safely possible
  • defer Rx and Cx until tumour progression
175
Q

what are the other symptoms of meningitis other than headache

A
  • fever/constitutional symptoms
  • photophobia
  • vomiting
  • neck stiffness on FLEXION
  • altered conscious state
  • vomiting
176
Q

what are the MS subtypes

A

relapsing remitting

secondary progressive

primary progressive