Histo: Neuro-Oncology Flashcards

1
Q

How much more common are secondary brain tumours than primary brain tumours?

A

10x more

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2
Q

Describe the radiological classification of brain tumours.

A
  • Extra-axial (coverings) - tumours of the bone, meninges and metastatic deposits
  • Intra-axial (parenchyma) - derived from normal cell populations of the CNS (e.g. glia, neurones, vessels) or derived from other cell types (e.g. lymphomas, metastases)
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3
Q

List the different cell types within the CNS that can give rise to brain tumours.

A
  • Neurons
  • Astrocytes
  • Oligodendrocytes
  • Ependyma
  • Choroid plexus epithelium
  • Meningothelial cells
  • Embryonal cells
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4
Q

What is the most common genetic syndrome associated with brain tumours?

A

Neurofibromatosis

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5
Q

What is the inheritance pattern of neurofibromatosis?

A

Autosomal dominant

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6
Q

Where are the genes that cause neurofibromatosis located?

A
  • NF1 = 17q11
  • NF2 = 22q12
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7
Q

List some manifestations of brain tumours that are:

  1. Supratentorial
  2. Subtentorial
A
  1. Supratentorial
    • Focal neurological defect
    • Seizures
    • Personality changes
  2. Subtentorial
    • Cerebellar ataxia
    • Long tract signs
    • Cranial nerve palsy
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8
Q

Outline the management options for brain tumours.

A
  • Surgery - aim for maximal safe resection with minimal damage to the patient. Debulking may be performed and biopsies may be taken.
  • Radiotherapy - used for gliomas and metastases
  • Chemotherapy - mainly for high-grade gliomas
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9
Q

What is the WHO classification of brain tumours based on?

A
  • Tumour type (cell of origin)
  • Tumour differentiation (grading)

NOTE: metastases are not graded

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10
Q

Outline the meaning of the different WHO grades for brain tumours.

A
  • Grade I = benign, long-term survival
  • Grade II = death in > 5 years
  • Grade III = death in < 5 years
  • Grade IV = death in < 1 years

NOTE: grades I and II are low

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11
Q

Which brain tumours are staged?

A

None

Except medulloblastoma

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12
Q

What is the most common type of primary brain tumour?

A

Glial tumours

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13
Q

How are the types of glial tumours seen in children and adults different?

A
  • Diffuse infiltration - mainly seen in adults, become more malignant with time, can either be astrocytomas or oligodendrogliomas
  • Circumscribe gliomas - mainly seen in children, tend to be low-grade, rarely undergo malignant transformation
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14
Q

Which genetic mutations are associated with gliomas in adults and in children?

A
  • Diffuse infiltration (adults) - IDH1/2
  • Circumscribed gliomas (children) - MAPK (BRAF)
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15
Q

List some examples of circumscribe gliomas.

A
  • Pilocytic astrocytoma (MOST COMMON)
  • Pleiomorphic xanthoastrocytoma
  • Subependymal giant cell astrocytoma
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16
Q

List some key features of pilocytic astrocytomas.

A
  • Usually grade I
  • Mainly occurs in children
  • Associated with NF1
  • Often cerebellar
  • BRAF mutation in 70% of cases
17
Q

What is the hallmark histological feature of pilocytic astrocytoma?

A
  • Piloid (hairy) cell
  • Often see Rosenthal fibres and granular bodies
  • Slow-growing with low mitotic activity
18
Q

List some key features of astrocytoma.

A
  • Usually Grade II-IV
  • Cerebral hemispheres are the most common site in adults
  • Can progress to become a higher grade (malignant progression)
  • IDH2 mutation in 80% of cases
  • Mitotic activity and vascular proliferation is absent
19
Q

What can astrocytomas eventually become?

A

Glioblastoma (after 5-7 years)

20
Q

What is the most aggressive and most common type of glioblastoma

A

De novo glioblastoma (stage IV)

21
Q

List some key features of glioblastoma multiforme.

A
  • Grade IV
  • Most patients > 50 years
  • High cellularity and high mitotic activity
  • Microvascular proliferation and necrosis
22
Q

What does glioblastoma multiforme tend to arise from?

A

90% arise de novo and have wildtype IDH

10% occur secondary to astrocytoma and have IDH mutation

23
Q

List some key features of oligodendrogliomas.

A
  • Grade II-III
  • Tends to present with a long history of neurological signs (usually seizures)
  • Slow-growing
  • Better prognosis than astrocytoma (better response to chemotherapy and radiotherapy)
24
Q

What is a characteristic histological feature of oligodendroglioma?

A

Round cells with clear cytoplasm (friend egg)

25
Which gene mutations are associated with oligodendroglioma?
IDH1/2 Co-deletion of 1p/19q
26
What is the second most common primary intracranial tumour after gliomas?
Meningioma
27
List some key features of meningioma.
* Mainly low grade (I and II) * Can be multiple (e.g. in NF2) * Can cause focal symptoms (e.g. seizures, compression)
28
Which histological feature of meningioma is important in determining grade?
Mitotic activity (number of mitoses per 10 high power fields) * Grade 1: \< 4 * Grade 2: 4-20 * Grade 3: \> 20 NOTE: brain invasion is also an important thing to assess (presence of brain invasion makes it grade II)
29
How does grade of meningioma affect the management options?
Grade II and III requires radiotherapy as well as surgery
30
What is a medulloblastoma?
* Embryonal tumour originating from neuroepithelial precurosrs of the cerebellum and dorsal brainstem * They are always found in the cerebellum
31
Describe the histological appearnce of medulloblastoma.
Small blue round cell tumour with expression of neuronal markers (very little differentiation) NOTE: snaptophysin is an example of a neuronal marker
32
What histological feature is suggestive of partial neuronal differentiation?
Homer-Wright rosettes
33
Outline the molecular classification of medulloblastoma.
* WNT-associated * SHH-associatd * Non-WNT/non-SHH
34
Which tumours most commonly metastasise to the brain?
* Lung * Breast * Melanoma
35
Where in the brain do metastases tend to be found?
* At the grey-white junction * This is because the cerebral blood vessels become smaller as they enter the white matter so neoplastic emboli get caught here