Brain Tumours Flashcards

1
Q

Who is more at risk of brain tumours - women on men?

A

women

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2
Q

What is the general presentation of brain tumours?

A

neurological deficit
motor weakness
headache (raised ICP signs too)
seizures

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3
Q

What is the first investigation for a suspected brain tumour?

A

MRI

CT if contraindicated

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4
Q

What is the best investigation for a suspected brain tumour?

A

biopsy

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5
Q

What are the majority of brain tumours?

A

METASASIS

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6
Q

Whats the most common type of primary brain tumours?

A

glioblastoma multiforme

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7
Q

Describe a grade 1 astrocytoma?

A

children/young adults
benign, slow growing
operate before it gets too big

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8
Q

Describe a grade 2 astrocytoma?

A

temporal or frontal lobe
malignant
poor prognosis if other risk factors

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9
Q

How do you treat a grade 2 astrocytoma?

A

surgery

then chemo and radiotherapy

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10
Q

Describe grade 3 anaplastic astrocytoma?

A

arises de novo

median survival 2 years

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11
Q

What appearance do grade 4 glioblastoma multiforme have on MRI?

A

butterfly appearance

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12
Q

Describe grade 4 glioblastoma multiforme?

A

spread via white matter
most common primary tumour
often in older patients 60-70s
median survival = 14 months

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13
Q

How do you treat grade 4 glioblastoma multiforme?

A

surgery and radiotherapy

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14
Q

Where are oligodendroglial tumours usually found?

A

frontal lobe

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15
Q

What is the presentation of oligodendroglial tumours?

A

25-45yrs
seizures
headaches

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16
Q

What do oligodendroglial tumours look like on MRI?

A

white toothpaste appearance

appear calcified

17
Q

What is the treatment of oligodendroglial tumours?

A

chemotherapy, surgery and radiotherapy

18
Q

What causes foster kennedy syndrome?

A

meningioma in the olfactory groove

19
Q

How does foster kennedy syndrome present?

A

optic atrophy in the ipsilateral eye

papillodema in the contralateral eye

20
Q

What are the characteristics of meningiomas?

A

90% are benign
females>males
arise from the meninges - think NF type 2

21
Q

What is the presentation of meningiomas?

A

CN palsy

headaches

22
Q

What investigation do you do for meningiomas?

A

MRI - see meningial involvement

CT - see bone involvement

23
Q

What is the treatment for meningiomas?

A

excise if causing a problem

CRAP ones reoccur - clear cell, choroid, rhaboid, papillary

24
Q

What is an acoustic neuroma?

A

nerve sheath tumour derived from schwann cells, arises in the cerebellopontine angle

25
What is the presentation of acoustic neuromas?
``` 30-50yrs hearing loss tinnitus balance problems hydrocephalus ```
26
What is the treatment of acoustic neuromas?
surgery and radiotherapy
27
How do Pineal tumours present?
``` parinaud syndrome (tumour of pineal gland) nystagmus coordination problmes headaches ```
28
Where do hemangioblastomas form?
posterior fossa
29
How do hemangioblastomas present?
benign cerebellar dysfunction symptoms raised ICP associated with von-hippie landau syndrome
30
What are the most common brain mets?
``` bronchus breast kidney thyroid colon ```
31
Where do most tumours arise in children?
below the tentorium cerebelli
32
Where do most tumours arise in adults?
above the tentorium cerebelli
33
What is the most common childhood cancer?
medulloblastoma
34
How does medulloblastomas present?
occur in the midline so distrupt CSF flow so present with hydrocephalus
35
What is the treatment for medulloblastomas?
radiotherapy