W21 - Neuro-oncology Flashcards

1
Q

What are primary vs secondary CNS tumours?

A

Primary CNS tumours - tumours that originated within the CNS

Secondary CNS tumours - metastases from other cancers (10x more frequent than primary tumours in adults)

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2
Q

In the adult population, are primary or seconary CNS tumours more common?

A

Secondary (mets) are 10x more common than primary CNS tumours

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3
Q

3 S/S for each of the following:

  • Intracranial hypertension
  • Supratentorial mass
  • Subtentorial mass
A

3 S/S for each of the following:

  • Intracranial hypertension = headache, vomiting, change in mental status
  • Supratentorial mass = focal neurological deficit, seizures, personality change
  • Subtentorial mass = cerebellar ataxia, long tract signs, cranial nerve palsy
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4
Q

___ imaging is the most important in neuroimaging

A

MR imaging is the most important in neuroimaging

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5
Q

In terms of surgical intervention in CNS tumours, what 3 surgeries could be possible?

A
  1. Craniotomy for debulking - subtotal and complete resections (as much tumour as possible)
  2. Open biopsy - inoperable but approachable tumours (about 1cm), usually representative
  3. Stereotactic biopsy - if open biopsy not indicated, about 0.5cm tissue, tissue may be insufficient
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6
Q

WHO classification of tumours looks at what 3 tumour parameters?

A
  1. Tumour type
  2. Tumour grade
  3. Tumour molecular profile
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7
Q

CNS tumour type is typically defined by the ________________

A

putative cell of origin / line of differentiation

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8
Q

The most common primary CNS tumours are _____, which could arise from these 3 lineages - name them.

A

The most common primary CNS tumours are gliomas, which could arise from these 3 lineages:

1. Astrocytes

2. Oligodendrocytes

3. Ependyma

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9
Q

CNS tumours - the grading system is an attemp to stratify tumours based on what?

A

by outcome, i.e. low grade = long survival, high grade = short survival

NB:

grade 1 - benign = long-term survival

grade 2 = more than 5 years

grade 3 = less than 5 years

grade 4 = less than 1 year

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10
Q

Diffuse vs circumscribed gliomas - comment on each of their:

  • grade
  • epidemiology
  • malignancy potential
A

Diffuse gliomas:

  • grades 2 or higher
  • epidemiology: adults, supratentorial
  • malignancy potential = malignant progression

Circumscribed gliomas:

  • grades 1-2
  • epidemiology: children, often posterior fossa
  • malignancy potential = rare
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11
Q

Diffuse vs circumscribed gliomas - comment on each of their genetic profiles

A

Diffuse gliomas: IDH1/2 muttions (30%), H2 mutations (1%)

Circumscribed gliomas: MAPK pathway mutations (i.e. BRAF)

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12
Q

The most common CNS tumour in 1st and 2nd decade of life is _______

A

The most common CNS tumour in 1st and 2nd decade of life is pilocystic astrocytoma (20% of CNS tumours below 14 yrs)

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13
Q

Pilocystic astrocytoma:

  • where is it commonly found?
  • MRI findings?
  • Histology findings?
  • Genetic profile?
A

Pilocystic astrocytoma:

  • where is it commonly found = cerebellar
  • MRI findings = well circumscribed, cystic, enhancing lesions
  • Histology findings = piloid “hairy” cells, slow growing, low mitotic activity
  • Genetic profile = BRAF mutations in 70%
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15
Q

Astrocytomas:

  • Where is it normally found?
  • Patient age?
  • MRI findings?
  • Histology findings?
  • Genetic profile?
A

Astrocytomas:

  • Where is it normally found = cerebral hemispheres (superficial, in white matter)
  • Patient age = 20-40s
  • MRI findings = T1 hypointense, T2 hyperintense, non-enhancing well-circumscribed lesion
  • Histology findings = low-to-modrate cellularity, low mitotic activity
  • Genetic profile = IDH1/2
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16
Q

Diffuse glioma:

  • where is it commonly found?
  • typical patient age?
  • Genetic profile?
A

Diffuse glioma:

  • where is it commonly found = supratentorial
  • typical patient age = 20-40s
  • Genetic profile = IDH mutants (imp becuse associated with good response to chemoradiotherapy)
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18
Q

IDH mutant can be found in _____ and ______

A

IDH mutant can be found in astrocytoma and glioma

19
Q

Glioblastoma multiforme:

  • median survival?
  • typical patient age?
  • where is it most commonly found?
  • MRI findings?
  • Histology findings?
  • IDH status?
A

Glioblastoma multiforme:

  • median survival = 8 months
  • typical patient age = >50
  • where is it most commonly found = cerebral hemispheres
  • MRI findings = heterogenous (due to necrosis/haemorrhage), enhancing post-contrast
  • Histology findings = high cellularity, high mitotic activity, necrosis

​- IDH1 WT normally (hence why they dont respond well to therapy

20
Q

IDH mutant astrocytoma/glioma will alwyas progress to higher grades (i.e. grade 3/4) typically in <10 years - T or F?

A

True

21
Q

Meningiomas:

  • % of primary CNS tumours?
  • typical age of presentation?
  • MRI findings?
A

Meningiomas:

  • % of primary CNS tumours = 38%
  • typical age of presentation = rare <40, incidence goes up with age
  • MRI findings = extra-axial, isodense, well-demarcated masses typically with cleft between tumour and brain
22
Q

The most aggressive and most frequent glioma is…

A

Glioblastoma multiforme

23
Q

In meningiomas, the grading is based on a combination of morphological tests, 2 of which are very imp - name them.

A
  1. Mitotic activity
  2. Microscopic brain invasion

(although these tumours are axial, sometimes they grow into the brain tissue so careful histo is imp)

24
Q

What does this MRI of the brain show?

A

Lots of metstases

26
Q

Meningiomas originate from _______ cells

A

Meningiomas originate from meningothelial cells of the arachnoid mater

28
Q

Meningiomas - what % is grade 1, grade 2, and grade 3?

Wht does each grade mean?

A

Meningiomas:

80% grade 1 (benign, recurrence <25%)

20% grade 2 (atypical, recurrence 25-50%)

1% grade 3 (malignant, recurrence 50-90%)

31
Q

4 most frequent tumours that give CNS metastases

A

Lung, breast, melanoma, renal cell carcinoma

32
Q

Medulloblastoma are ______ tumours, originating from _______ cells

A

Medulloblastoma are embryonal tumours, originating from neuroepithelial/neuronal cells

33
Q

Medulloblastoma:

  • typical grade?
  • typical location in brain?
  • outcome?
A

Medulloblastoma:

  • typical grade = high (grade 4)
  • typical location in brain = cerebellum or brainstem
  • outcome = good outcome with radio-chemo
34
Q

Methylome profiling of certain CpG islands in CNS tumours - what does it show us?

A

The methylation profile is stable in CNS tumours and reflects the tumour cell origin

35
Q

What is the most frequent brain tumour in children?

A) Glioblastoma, IDH WT, grade 4

B) Pilocystic astrocytoma, grade 1

C) Medulloblastoma, grade 4

D) Astrocytoma, IDH mutant, grade 2

A

B) Pilocystic astrocytoma, grade 1

36
Q

Wht is the most frequent brain tumour in adults?

A) Glioblastoma, IDH WT

B) Metastatic deposit

C) Meningioma

D) Astrocytoma, IDH mutant

A

B) Metastatic deposit

37
Q

Which mutation identifies diffuse astrocytic tumours with a better prognosis?

A) IDH mutation

B) BRAF mutation

C) EGFR mutation

D) H3 mutation

A

A) IDH mutation

38
Q

45 year old, headache, previous pulmonary lobectomy, CT shows crontal lesion. What is your diagnosis?

A) Glioblastoma, grade 4

B) Astrocytoma, grade 2

C) metastatic carcinoma

D) Meningioma, grade 1

A

C) metastatic carcinoma

39
Q

5 yer old, headache, vomiting, papilloedema. MRI brain shows cystic cerebellar lesion. What is your diagnosis?

A

Pilocystic astrocytoma

40
Q

70 year old with left arm and leg weakness and seizures. MRI shows heterogenous enhancing right frontal lesion. Your diagnosis:

A) Glioblastoma, grade 4

B) Meningioma, grade 1

C) Metastatic carcinoma

D) Astrocytoma, grade 2

A

A) Glioblastoma, grade 4