Brain, meningeal, neural tumours Flashcards

1
Q

Aetiology brain tumours?

A
  • Few clearly defined RFx
  • Ionising radiation (eg. radiotherapy/nuclear accident) increased risk meningioma and glioma
  • No proven role electromagnetic radiation, other environmental
  • Predisposing conditions
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2
Q

Which conditions predispose to brain tumours?

A
  • Neurofibromatosis 1 and 2

- Li Fraumeni Syndrome (p53 oss predisposes to glioma)

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3
Q

Why are headaches worse in the morning?

A
  • Increased blood return when prone

- Hypoventilation: increased CO2 ==> cerebral swelling

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4
Q

What are the causes of cerebral mass effect progressing over several weeks?

A
  • Primary brain tumour
  • metastatic brain tumour
  • brain abscess
  • chronic subdural haematoma
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5
Q

How is malignant astrocytoma defined histologically?

A
  • Hypercellularity
  • Cellular atypia and pleomorphism
  • nuclear atypic/pleomorphism
  • Mitoses
  • Endothelial hyperplasia
  • Necrosis/pallisading necrosis
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6
Q

How may an intracranial mass present?

A
  • Symptoms of raised ICP
  • Seizures
  • Focal neurological deficit
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7
Q

What is the Monro-Kellie doctrine?

A

Cranial cavity rigid, increase in contents causes rise in pressure.
Some capacity for compensation but once critical point reached, small increases in volume result in large increases in ICP.

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8
Q

What are the components of the cranial cavity (in order of importance)?

A

1) Brain
2) Arterial blood
3) Venous blood
4) CSF

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9
Q

How does a rise in ICP alter the contents of the cranial cavity? (Related to Monro Kellie curve)

A

Get rid of contents from least to most important (i.e remove CSF -> venous blood ==> flat part of curve). Once arterial supply decreased ==> confusion. Hence steep part of curve.

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10
Q

Rx of malignant astrocytoma?

A
  • Steroid (dexamethasone): reduce oedema and ICP
  • Resect as much as possible
  • Adjuvant: radiotherapy, chemotherapy
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11
Q

What is FLAIR MRI?

A

Fluid attenuated inversion recovery.

System represses signal from normal CSF (allows better visualisation of lesions near ventricles etc.)

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12
Q

What is the pathology of low grade glioma?

A

-As for malignant astrocytoma but less abnormal for:
-hypercellularity
-cellular atypia/pleomorphism
-nuclear atypic/pleomorphism
Very few mitoses, no necrosis, invades diffusely, may have calcifications.

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13
Q

What are low grade gliomas?

A

Oligodendroglioma
Astrocytomas
Mixed forms

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14
Q

Common age of onset low grade glioma?

A

Often young (25-45).

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15
Q

Survival of low grade glioma?

A

Prolonged (years to decades).

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16
Q

What is a feature of metastatic brain tumours on FLAIR MRI?

A

Often cause intense cerebral oedema that causes more symptoms than the tumour mass.

17
Q

What are the common primary tumour sites causing brain metastases?

A
  • Lung Ca
  • Breast Ca
  • Metastatic melanoma
  • Renal Ca
  • GIT Ca
  • Unknown primary (15%)
18
Q

How are brain metastases treated?

A
  • Steroids (dexamethasone)

- Surgical removal of mets if indicated

19
Q

When is surgery to remove brain mets indicated?

A
  • If met is solitary
  • If primary disease is stable
  • If primary unknown (remove to confirm diagnosis)
  • Multiple mets may be removed for palliation (i.e. relieve disabling symptoms)
20
Q

Characteristics of meningioma?

A
  • Most common benign brain tumour
  • Most common in middle age
  • W>M
  • Cause intense oedema
21
Q

Where do meningiomas arise?

A

Arachnoid cells in the meninges

22
Q

Where do meningiomas characteristically occur?

A

Falx, convexity and sphenoid wing.

Each has characteristic clinical syndrome.

23
Q

Pathology of meningioma?

A
  • “Whorls”
  • Multiple subtypes
  • Malignancy infrequent
24
Q

Rx of meningioma?

A
  • Total surgical excision

- Subtotal excision and diathermy of dural attachment if complete excision not possible