brain tumours Flashcards

1
Q

symptoms parietal legions (4)

A

loss of sensation, apraxias (maths, writing), astereognosis (can’t identify an object by touch), contalateral inferior quadrantanopia

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2
Q

symptoms occipital legions (4)

A

hemioanopia + macular sparing // cortical blindess// visual agnosia // hallucinations

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3
Q

symptoms temporal legion (3)

A

wernickes aphasia (word substitution, neologism // superior quadrantopia // emotion and memory issues

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4
Q

frontal lobe legions (5)

A

disinhibition! // expressive (brocas) aphasia: non-fluent speech // asomnia // weakness // preservation

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5
Q

cerebellar legion symptoms

A

gait and ataxia // tremor // vertiga // nystagmus // dyskinesia

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6
Q

what can a legion in the thalamus or hypothalamus cause

A

wernickes or korsakoff

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7
Q

legion in subthalmic nucleus of basal ganglia symptoms

A

sudden, flinging movements

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8
Q

legion in caudate/ striatum nucleus of basal ganglia symptoms

A

huntington chorea

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9
Q

legion in substantia nigra of basal ganglia symptoms

A

parkinsons

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10
Q

general symptoms brain tumour

A

extreme headache (worse lying down + wakes you) // worse on cough // seizure // visual defects // papilledema

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11
Q

where are the majority of tumours in children

A

infratentorial –> ataxic gait + tiptoeing

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12
Q

invx brain tumour

A

CT or MRI

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13
Q

seizure and raised ICP tumour mx

A

phenytoin // mannitol + dexamethasone

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14
Q

mx brain tumour

A

surgery +/- radio or chemo

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15
Q

most common type of brain tumours

A

gliomas esp astrocytoma

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16
Q

who usually gets gliomas

A

children and young adults 20-30

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17
Q

most common glioma in children

A

pilocytic astromcytoma

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18
Q

different grades of glioma

A

I = pilocytic glioma // II = oligodendrogioma // III = anaplastic astrocytoma // IV = glioblastoma multiforme

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19
Q

what symptoms can pilocytic astrocytomas cause in children

A

laughing seizures

20
Q

where do oligodendrogliomas usually form

A

frontal lobe

21
Q

histology oligodendrogliomas

A

invade subarachnoid –> grey pink toothpaste appearance

22
Q

age glioblastoma multiform

A

60-70

23
Q

MRI glioblastoma multiforme

A

butterfly

24
Q

chemo for glioblastoma

A

temozolomide

25
Q

mx for oedema in brain tumours

A

dexa

26
Q

most common primary brain tumour adults

A

glioblastoma

27
Q

2nd most common brain tumour adults

A

meningioma

28
Q

where do meningionas arise from

A

arachnoid cap cells - usually next to dura

29
Q

where do vestibular schwannomas typically arise

A

cerebellopontine angle on CNVIII

30
Q

what is bilateral vestibular schwannomas assoc with

A

NF2

31
Q

symptoms vestibular schwannomas

A

age 30-50 // sensorineural hearling loss // loss of corneal reflex // facial nerve palsy // tinnitus

32
Q

where do hermangioblastomas usually form

A

vascular tumour of cerebellum

33
Q

what is hermangioblastoma assoc with

A

von HL syndrome (multiple hermangiomas)

34
Q

symptoms hermangioblastoma

A

cerebellar symptoms

35
Q

where do ependymomas form + what symptoms

A

4th venticles, hydrocephalus

36
Q

most common supratentorial paeds tumour

A

Craniopharyngioma

37
Q

symptoms + invx Craniopharyngioma

A

hormonal disturbance, hydrocephalus, bitempiral hemianopnia // MRI + endocrine profile

38
Q

who gets medulloblastoma/ where do they arrise

A

children, aggressive, cerebellum

39
Q

where does medulloblastoma spread too

A

down CSF and spinal cord // crumbly appearance

40
Q

mx medulloblastoma

A

radio + resection

41
Q

common brain mets (most –> least)

A

lung –> breast –> bowerl –> melanoma –> kidney –> thyroid

42
Q

what inheritance is von hippel lindae

A

autosomal dominant chromsome 3

43
Q

symptoms legion cerebellar hemisphere

A

peripheral ‘finger nose’ ataxia

44
Q

symptoms legion cerebellar vermis

A

central ataxia

45
Q

where in brain are mengiomas found

A

falx cerebri, superior sagittal sinus, convexity or skull base.