Brain Tumours Flashcards

(63 cards)

1
Q

general presentation of brain tumours

A
  • progressive focal neurological deficit
  • motor weakness
  • raised ICP features (headache)
  • seizures
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2
Q

acute onset of symptoms?

A

tumour can cause eg if starts bleeding

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3
Q

name 4 supratentorial herniations

A
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4
Q

what happens in an uncal herniation

A

the medial part of the temporal lobe (uncus) herniates inferiorly to the tentorium cerebelli

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5
Q

which type of herniation can damage CNIII

A

uncal - ipsilateral fixed blown pupil

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6
Q

describe ICP headache

A
  • awaken them from sleep
  • exacerbated by couging, sneezing,bending
  • worse on lying down
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7
Q

raised ICP features

A
  • vomiting without nausea
  • ocular palsy
  • back pain
  • papilloedema - bilateral
  • alteredlevel of consciousness
  • seizures
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8
Q

cushings triad

A

Cushing’s triad: increase in systolic and pulse pressure, bradycardia and irregular respiration

  • Raised ICP to the point where it exceeds MABP, this causes the arterioles in the brains cerebrum to become compressed. Compression results in cerebral ischaemia
  • Activation of sympathetic and parasympathetic nervous system. At this stage sympathetic is activated more and causes hypertension and tachycardia
  • Baroreceptors in the aortic arch detect this and trigger a parasympathetic response via CNX, induces bradycardia
    • Bradycardia may be caused due to direct mechanical distortion of CNX
  • Increased pressure on the brainstem (control of breathing) results in irregular respiratory pattern
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9
Q

presentation of frontal lobe problem

A
  • contralateral weakness due to deficit in M1
  • personality changes - disinhibition and cognitive slowing
  • urinary incontinence due to disruption of micturition inhibition centre
  • gaze abnormalities - frontal eye field involvement
  • expressive dysphasia/aphasia if Brocas area on left is involved
  • seizures
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10
Q

presentation of temporal lobe problem

A
  • memory deficits
  • receptive aphasia/dysphasia for left sided lesions if Wernickes area involved
  • contralateral superior quadrantopia
  • seizures
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11
Q

presentation of parietal lobe problem

A
  • contralateral weakness and sensory loss due to deficit in S1
  • contralateral inferior quadrantopia
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12
Q

parietal lesion on dominant lobe presentation

A

dyscalculia, dysgraphia, finger agnosia, left right disorientation if dominant lobe affected –> gerstmann syndrome

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13
Q

parietal lesion on non dominant lobe presentation

A

neglect (not aware of one side of the body), dressing and constructional apraxia

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14
Q

occipital lobe lesion presentation

A

contralateral homonymous hemianopia, visual hallucinations (V1)

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15
Q

cerebellum lesions presentation

A
  • ipsilateral ataxia
  • n and v
  • dizzines and vertigo
  • slurred speech
  • intention tremor
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16
Q

what does toe walking in children indicate

A

cerebellar problem

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17
Q

very first investigation

A

fundoscopy to check for papilloedema

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18
Q

imaging

A
  • CT is done first - quickest and widely available
  • MRI gives better tissue definition and can be used to grade tumours
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19
Q

what imaging is good for bleeds

A

CT for acute bleed, MRI for chronic/old bleeds

bleed on left, infarct on right

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20
Q

imaging in children

A

avoid CTs as they do a lot of harm, MRI is preferred

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21
Q

what should be suspected when an older person presents with possible brain tumour

A

metastases - always take a cancer history! (haemoptysis, melaena, change in bowel habits, PR bleeding)

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22
Q

what are the characterstics of grade I tumours and who do they occur in

A
  • slow growing, benign
  • children and YP
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23
Q

pilocytic (low grade I tumours) - who gets them

A

children and young adults

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24
Q

pilocytic astrocytoma - pathology

A

bipolar cells with long hair like projections

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25
management of pilocytic astrocytomas
surgery, high curative rate. have sharply defined edges so are easily removed
26
where do pilocytic astrocytomas usually arise
cerebellum, brainstem or midline structures, eg thalamus and optic chiasm
27
which condition are pilocytic astrocytomas in the optic chiasm seen in
NF1
28
low grade type II tumours prognosis
* are less histologically stable and have the potential to transform to high grade gliomas
29
what symptom do type II tumours often present with
seizures
30
common presentation of oligodendrogliomas
seizures and headaches
31
common age of presentation fo oligodendrogliomas
25-45
32
what appearance does a oligodendrogliomas often have after invading teh subarachnoid space
toothpaste appearance
33
prognosis of oligodendrogliomas
best
34
where do oligodendrogliomas tend to arise
frontal lobe of cerebral hemispheres and can affect white matter and cortex
35
where do diffuse astrocytomas tend to arise
frontal and temporal lobes
36
common presentation of diffuse astrocytomas
seizures
37
which age group gets diffuse astrocytomas
young adults
38
managment of grade II tumours
surgery and radio and chemo diffuse astrocytomas are harder to remove as they do not have well defined edges
39
do grade III tumours arise de novo or do they progress from grade I and II
either
40
what is the median survival of grade III tumour
2 years
41
what is the median survival of grade IV tumour
\<1 year
42
what is the most common type of grade IV tumour
glioblastoma
43
what age group gets GBM
older people
44
MRI appearance of GBM
butterfly appearance
45
further tests of GBM after MRI
* histological sample * tissue molecular analysis to predict response to alklyating agent chemotherapy (temozolamide)
46
can you cure grade III and IV tumours
no, can improve survival
47
management of grade III adn IV tumours
chemo radio and surgery -Stupp protocol - improves median survival
48
what agent is used for chemo
temozolomide - alkylating agent
49
meningiomas
* usually benign tumours that arise from residual mesenchymal cells in the meninges (arachnoidal cap cells in arachnoid membrane) * rarely malignant, grow slowly
50
presentation of meningioma
* most are asynmptomatic * symptoms of raised ICP
51
what age group gets meningiomas
elderly females (6 and 7 decade)
52
what condition is assoicated with multiple meningiomas
NF2 (also bilateral acoustic neuroma)
53
Foster Kennedy syndrome
can be caused by meningioma in olfactory groove optic atrophy in the ipsilateral eye (direct pressure on eye) and papilloedema in the contralateral eye (raised ICP)
54
where do acoustic neuromas most ocmmonly arise from
cerebellopontine angle
55
where do acoustic neuromas arise from
schwann cells, vestibular portion of CNVIII
56
how do acoustic neuromas present
* **Progressive ipsilateral tinnitus ± unilateral sensorineural deafness** (cochlear nerve compression) **± vertigo** * Loss of corneal reflex * Headache * Suspect in any patient with unilateral hearing loss * cause raised ICP when bigger
57
pathology of acoustic neuromas
Verocay bodies
58
preferred imaging of meningioma
MRI
59
which other CN can acoustic neuromas affect
CNVII - facial numbness and tingling
60
wht should be suspected if patient is young and has bilateral acoustic neuromas
NF2 (multiple meningiomas too)
61
haemangioblastomas
benign, cystic, highly vascular tumours
62
where do haemangioblastomas develop
posterior fossa - cerebllar dysfunction and raised ICP
63
which syndrome are haemangioblastomas associated with
VHL