Hi - Neuro-Oncology Flashcards

1
Q

Classifications of tumours in brain

A

Primary - CNS derived
Secondary - mets

Extra-axial - coverings eg bone, skin, meninges, nerves
Intra-axial - glia, neurones, neuroendocrine cells, lymphomas and germ cell tumours

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2
Q

Which types of CNS tumours are benign / malignant?

A

Intra-axial = benign
Extra - axial and secondary = malignant

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3
Q

Aetiology of brain cancers?

A

Unknown
Prev H+N radiotherapy
Some familial eg neurofibromatosis

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4
Q

What % of:
- adult brain cancers are primary tumours ?
- childrens brain cancers are primary tumours?

What is the comparative freq of secondary vs primary ?

A

Primary tumours are 1% of all adult cancers and 25% childrens
Secondary 10x freq primary

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5
Q

Functions of neuroimaging in neuro oncology

A

Assess tumour type
Guide biopsy / resection
Post surgery / Tx response
Follow up / recurrence / progression

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6
Q

3 Mx options for neuro onc

A

Surgery - resection with minimal damage to normal tissues
Radio - gliomas, mets
Chemo - high grade gliomas and some lymphomas

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7
Q

WHO grading for neuro tumours

A

ABOUT SURVIVAL
1 = Benign
2 = > 5 years
3 = < 5 years
4 = < 1 years

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8
Q

Give features of diffuse gliomas, including age group and usual grade

A

Perivascular spread and supratentorial
In adults mainly
Grade 2+

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9
Q

How does the IDH mutant affect glioma prognosis?

A

IDH+ = increased prognosis and response to Tx

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10
Q

Who gets circumscribed gliomas?

A

Kids

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11
Q

What is the most common brain tumour in children?

A

Pilocytic astrocytoma

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12
Q

MRI features of Pilocytic astrocytoma
where are they found?

A

well circumscribed, cystic, enhacning lesion
In cerebellum / brainstem / optic hypothalamus

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13
Q

Histology of Pilocytic astrocytoma

A

BRAF+ in 70%
Hairy on histology - rosenthal fibres
Piloid cells
Slow growing, low mitotic activity

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14
Q

Grade of Pilocytic astrocytoma

A

1

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15
Q

Features of astrocytoma (age range, histology, prognosis)

A

20-40 year old
Low or normal mitotic activity with no vascular proliferation/necrosis.
Progresses to higher grade over time

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16
Q

What is the worst brain tumour?

A

Glioblastoma multiforme

17
Q

Grade of GBM & prognosis

A

4 - under 8 months

18
Q

Mutations in GBM

A

IDH1 wildtype (NO mutation)
TERT / PTEN / EGFR

19
Q

GBM histology

A

Very cellular, no clear margins
Neoangiogenesis
Necrosis

20
Q

Grades and % of meningiomas

A

G1-3
80% G1
20% G2 (25-50% recur)
1% G3 (50-90% recur)

21
Q

Markers of meningiomas

A

TERT or metholome

22
Q

Epidemiology of meningioma

A

38% of CNS tumours
Rare under 40 years old, increase with age

23
Q

MRI apperance of meningiomas

A

Well circumscribed, non invasive

24
Q

Grading of Ki67 mitotic activity

A

G1 = <4
G2 = 4-20
G3 = 20+

25
Q

Describe appearance of CNS mets and location

A

Often multiple
At grey/white matter junctions or leptomeningeal

26
Q

Which Ca are most likely to met to brain?

A

Lung, breast, melanoma, renal Ca

27
Q

Who gets medulloblastomas?

A

RARE
2nd most common brain cancer in KIDS tho

28
Q

Where are medulloblastomas from?

A

Embryonal cells

29
Q

Histology of medulloblastomas

A

Poor differentiation
Synaophysin
GFAP
Ki67 markers are HIGH

30
Q

What is the purpose of the methylome profile?

A

Reflects tumour cell origin in poorly differentiated tumours when compared to reference ranges