Tumours of the CNS Flashcards

(47 cards)

1
Q

what are the most common CNS tumours

A

gliomas, meningiomas

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2
Q

what is the occurrence distribution of tumours of the nervous system

A

age distribution is bimodal

Adults: cerebrum, glioma and menigioma.

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3
Q

where are tumours commonly found in children in the cerebrum or cerebellum

A

cerbellum (PNET and medullablastoma)

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4
Q

where are tumours commonly found in adults in the cerebrum or cerebellum

A

Glioma and Meningioma

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5
Q

do males have a increased risk of glioma or meningioma

A

glioma

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6
Q

do females have an increased risk of glioma and meningioma

A

meningioma

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7
Q

are neuronal tumours common or rare

A

rare

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8
Q

Do neurones communicate with the blood supply

A

no

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9
Q

how many astrocytes are there per neurone

A

10 astrocytes

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10
Q

define astrocyte

A

support and protect

connect neurones with blood supply so that they can access the metabolites they need to function.

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11
Q

define oligodendrocyte

A

myelin- insulate neurones

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12
Q

define ependymal cells and choroid plexus cells (CSF)

A

produce CSF
protect brain from trauma
control external environment

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13
Q

define micoglia defense

A

comes from bone arrow

sends astrocytes signal so that inflammatory cells can enter the blood brain barrier.

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14
Q

what are the 4 types of glial cells (support cells)

A

astrocytes
oligodendrocytes
ependymal cells and choroid plexus
micoglial cells (defense)

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15
Q

what is tumour of the neurone known as

A

ganglioma

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16
Q

what is tumour of the glial cells known as

A

glioma

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17
Q

what is tumour of the meninges known as

A

meningioma

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18
Q

how many layers is the cerebrum

A

6 layers

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19
Q

how many layers is the cerebellum

20
Q

how are CNS tumours diagnosed

A

Histology- name of tumour

biological behaviour- grade of the tumour.

21
Q

do you have micoglial tumours

22
Q

what are the characteristic features of a benign tumour

A
slow growing
respect surrounding tissue
no/ slow progression
no recurrence
surgery -depends on postion
23
Q

what are the characteristic features of a malignant tumour

A
rapid growing
invade and destroy surrounding tissue
progress
recurrent
surgery and adjuvant therapy (radiotherapy and chemotherapy)
24
Q

what grade are benign tumours

25
are all graded tumours malignant
No | grade one can be benign.
26
what histological changes are present in a malignant tumour
cell size and shape mitotic activity Necrosis-TNF to kill other cells vascular proliferation- increase endothelial cells to supply tumour.
27
what are the 3 types of gliomas
Astrocytic tumours Oligodendroglioma Ependymoma
28
what are the 2 types of nerve sheath tumours
Schwannoma and neurofibroma
29
Microscopical features of astrocytic tumours
Fine fibrillary and microcystic background Increased cellular density Pleomorphism ( variation in size, shape and chromasia)
30
what are the features of diffuse astrocytoma II
infiltrative, micro cystic fibrillary, low cellular density mild atypia no mitotic activity- grade 2
31
what are the features of Anaplastic astrocytoma III
Moderate cellular density Moderate Pleomorphism Mitoses - grade 3
32
what are the features of glioblastoma
High cellular density and mitoses Vascular proliferation Necrosis Histology- necrosis occurring in the centre and tumour cells are trying to escape
33
is the men age for developing glioblastma younger or older than anapaestic astrocytoma
older
34
what are the features of pilocytic astrocytoma
``` Children, cerebellum Well-defined, cystic Pilocytes Rosenthal fibres Vascular proliferation ```
35
what are the features of oligodendroglioma II/III
Round uniform nuclei with clear cytoplasm (fried-egg appearance) Arborising capillaries (chicken wire) Calcifications
36
what are the main features of Ependymoma II / III
Well-defined tumour, ventricles Pseudorosettes Round small uniform cells
37
what are the main features on meningioma
Females, dura, adults Well-defined extra-axial tumour Whorls, psammoma bodies Histology- tumour cells whirl around each other.
38
what are the main features of PNET
``` Children, cerebellum Very high cellular density- no cytoplasm seen in histology. Anaplastic hyperchromatic cells Frequent mitoses and apoptosis Rosette formation ```
39
what are the main features of
``` Spindle-cell tumours Schwannoma I – 8th cranial nerve – Biphasic pattern: loose and dense areas – Reticulin rich Neurofibroma I – Spinal nerves – Rich in collagen ```
40
what causes meningioma
radiotherapy
41
what causes lymphoma
immunosupression
42
what causes familial syndromes
NF1, NF2
43
Mutations in any of Wnt 7, SHH and notch leads to what
tumours.
44
MGMT promoter methylation is a predictive marker of which type of CNS tumour to akylating chemotherapy
glioblastomas
45
1p/19q deletion is a predicative marker of n prognosis of what CNS tumour is patients receiving adjuvant radio and/ or chemotherapy.
(oligodendro)glial tumor
46
What CNS tumours are IDH1/IDH2 mutations a diagnostic marker for
II and III gliomas as well as secondary glioblastomas
47
What CNS tumours use BRAF duplication/fusion to determine the diagnosis of tumours.
Diagnostic marker for pilocytic astrocytomas, helpful to distinguish these from diffuse astrocytomas