CNS tumors Flashcards

1
Q

what is the most common type of intracranial tumour

A

those of neuroepithelial origin (glial cells - astrocytes and oligodenrocytes) - that being astocytoma (glioma)

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2
Q

what is WHO classification of gliomas

A

grades I and II are benign and common in children
grades III is called anaplastic astrocytoma
grade IV is called glioblastoma multiforme, it is most commonly detected and is the most malignant grade

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3
Q

what are the mechanisms by which you can get glioblastoma multiforme

A

increasing mutations which can occur directly from a grade I neoplasm (progressive pathway) or directly from a precursor cell (de novo pathway)

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4
Q

glioblastoma multiforme appearance on imaging

A

peripheral enhancement which is irregular
a central necrotic core which does not enhance with contrast
there is also surrounding oedema

it travels along white matter tracts, it can cross the corpus callosum, and can give an appearance similar to B cell lymphoma

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5
Q

what is the aetiology of brain tumours

A

largely unknown
factors that have increased predisposition:
- previous head injury
- carcinogen exposure
- immunosuppression
- ionising radiation exposure (former tinea capitis Tx)
- small hereditary component

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6
Q

Meningiomas

A

are benign tumours of the arachnoidal cells and can occur anywhere along the dura

it is infrequently detected, more common in females, and more common in the elderly

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7
Q

CNS metasis

A
common for:
- lung cancer
- breast cancer
- renal cancer
- colon cancer
and malignant melanoma

there are usually multiple metastatic lesions, which are ring enhancing, and are subcortical with vasogenic oedema

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8
Q

Presenting signs of brain tumours

A
  • vomiting and nausea
  • headaches (worse supine, and you wake up with the headache)
  • focal neurological signs (from mass effect)
  • drowsiness
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9
Q

Pituitary adenomas

A

are associated with optic chiasm compression and Px with

  • bitemporal hemianopia
  • opthalmoplegias or oculomotor palsies
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10
Q

What are the most common pituitary adenoma

A

Prolactinoma - gynaecomastia
GH-oma - produce acromegaly facies

most are null-omas (produce no hormone)

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11
Q

Common cranial and peripheral nerve tumours

A
  • Schwannoma

- Neurofibroma

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12
Q

Contrast between neurofibromas and schwannomas

A

Schwannomas are benign and present later in life, are more common in females

Neurofibromas are more common than Schwannomas, contain a mixed cell type, and are difficult to excise

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13
Q

The who familial neurofibromas are

A

type I - has widespread cafe au lait spots (chromosome 17)

type II - is rarer - usually acoustic neuromas (benign)

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14
Q

Paediatric CNS tumours are second to leukaemia what are they

A

70% are in the posterior fossae or the infratentorium

most common is - medulloblastoma - embryonic origin
next common -pilocytic astrocytoma is common is associated with a benign cystic mass within the cranial cavity

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15
Q

What genetic disorder predisposes you to CNS neoplasia

A

von Hipple Lindau Syndrome (very rare)

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16
Q

Neurons are

A

the functional cells of the nervous system and are classed primarily on shape

17
Q

Glial cells are

A

These cells outnumber the neurons of the body and are actively dividing (unlike neurons), and are regarded as neuron supporting cells, because of their active cell division they are privy to neoplastic transformation

they include

  • astrocytes (which control the local environment of the neuron)
  • microglia - which are the macrophages of the neurons, absorb debris and are at sites of injury
  • oligodendrocytes - make up CNS myelin
  • Schwann cells - make up PNS myelin