Brain Tumours Flashcards

1
Q

most common extra-axial brain tumour?

A

meningioma

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2
Q

features of meningioma?

A

benign
arise from residual mesenchymal cells in meninges
cause symptoms by compressing underlying brain

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3
Q

other types of extra-axial brain tumour?

A

pituitary adenoma
craniopharyngioma
choroid plexus tumour
acoustic neuroma

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4
Q

most common presenting features of brain tumours in general?

A

headache
progressive neurological deficit
motor weakness
seizures

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5
Q

features of brain tumour headache?

A

worse in morning
causes waking
worse on coughing, vomiting, leaning forward etc
can be associated with vomiting
can be similar to migraine/tension headache in some cases

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6
Q

what causes headache in brain tumour?

A

raised ICP
invasion/compression of dura, BVs, periosteum
can be 2ndary to diplopia (straining to focus etc)
extreme hypertension (cushings triad in raised ICP)
psychogenic (worrying about symptoms etc)

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7
Q

what is cushings triad?

A

triad of physiological responses to raised ICP

  • increased BP
  • reduced HR
  • reduced RR
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8
Q

deficits in frontal lobe tumour?

A
movement problems
thought and reasoning affected
behaviour changes
memory problems 
perseveration
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9
Q

what is perseveration?

A

the repetition of a particular response (such as a word, phrase, or gesture) regardless of the absence or cessation of a stimulus

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10
Q

deficits in perietal lobe tumour?

A

dyspraxia
sensation problems
neglect
intellect

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11
Q

deficits in temporal lobe tumour?

A

hearing and vision pathways

emotion

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12
Q

visual field defect in temporal lobe lesion?

A

superior quadrantanopia

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13
Q

deficits in occipital lobe lesion?

A

visual field defect
left = speech, motor and sensory function
right = abstract concepts

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14
Q

deficits in cerebellar lesion?

A
DANISH
- dysdiadokinesia
- ataxia
- nystagmus
- intention tremor
- slurred speech (dysarthria)
- hypotonia 
also have problems with balance and coordination
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15
Q

investigations in brain tumours?

A
CT
MRI
lumbar puncture
PET scan
lesion biopsy
EEG
angiogram
radionucleotide studies
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16
Q

potential sites for brain tumours?

A
meninges
neuroepithelial tissue
nerve sheath cells
developmental lesions
germ cells
local extension from adjacent structures
metastases
haematopoietic/lymphomas
17
Q

types of neuroepithalial tissue?

A
astrocytes - mainly
oligodendrocytes - mainly
ependymal cells/choroid plexus
neuronal cells
embryonic
pineal cells
18
Q

astrocyte and oligodendrocyte derived tumours are known as what?

A

glial tumours

19
Q

grade 1 astrocytic tumour?

A

pilocytic astrocytoma/pleomorphic xanthoastrocytoma
benign and slow growing (cannot become malignant)
common in children and young adults
can occur in optic nerve, hypothalamus, cerebellum, brainstem

20
Q

grade 1 astrocytic tumour management?

A

surgery (usually curative)

21
Q

grade 2 astrocytic tumour?

A

low grade astrocytoma
can be fibrillary, gemistocytic or protoplasmic
can become malignant if left
often presents with seizures

22
Q

pathology features of grade 2 astrocytic tumour?

A

hypercellular
pleomorphism
vascular proliferation
necrosis

23
Q

how is grade 2 astrocytic tumour managed>

A

surgery +/- chemotherapy, radiotherapy or both

24
Q

grade 3 astrocytic tumour?

A

anaplastic astrocytoma

can arise de novo

25
Q

median survival of grade 3 astrocytic tumour (anaplastic astrocytoma)?

A

2 years

26
Q

management of grade 3 astrocytic tumour?

A

surgery + post op external beam radiotherapy

not curative but gives cytoreduction and reduces mass effect

27
Q

grade 4 astrocytic tumour?

A

glioblastoma multiforme
(most common primary brain tumour)
spreads via white matter tracts and CSF pathways
can have multiple gliomas

28
Q

median survival of glioblastoma multiforme?

A

<1 year

29
Q

how many glial tumours are derived from oligodendrocytes?

A

20%

30
Q

where do oligodendroglial tumours often arise?

A

usually in frontal lobe

31
Q

how do oligodendroglial tumours present?

A

usually 25-45 year olds

presents with seizures often

32
Q

how can oligodendroglial tumours be differentiated from astrocytomas?

A

calcification (usually peripheral)
cysts
peritumoral haemorrhage

33
Q

other pathology features of oligodendroglial tumours?

A

solid and grey/pink on cut surface
toothpaste morphology
mucinous change

34
Q

how are oligodendroglial tumours managed?

A

chemotherapy
surgery + chemo
radiotherapy can reduce seizures
PVC chemo + radiotherapy = doubled survival

35
Q

median survival of oligodendroglial tumours?

A

10 years

36
Q

where do meningiomas derive from?

A

arachnoid cap cells

extra-axial

37
Q

what are meningiomas associated with?

A

breast cancer

NF2

38
Q

where can meningiomas occur?

A

parasagittal
convexity
sphenoid
intraventricular

39
Q

how do meningiomas present?

A

usually asymptomatic
can have headaches
can cause cranial nerve neuropathies if in skull base