Brain Tumours Flashcards

1
Q

WHO classifications of CNS tumours

A
Tumours of neuroepithelial tissue 
Tumours of meninges 
Tumours of cranial and spinal nerves 
Haematopoietic neoplasma 
Germ cell tumours 
Cysts and tumour-like lesions 
Tumours of the sellar region 
Local extensions from regional tumours 
Metastatic tumours
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2
Q

Common primary types of brain tumours

A

Neuroepithelial tissues - glioma
Meninges - meningioma
Pituitary - adenoma

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3
Q

Commons secondary types of brain tumours (spread from)

A
Renal cell carcinoma 
Lung carcinoma 
Breast carcinoma 
Malignant melanoma 
GI tract carcinoma
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4
Q

Pathological features of gliomas

A

Derived from astrocytes

WHO grade I - IV

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5
Q

Pathological features of grade IV gliomas

A

Most common and most aggressive
Glioblastoma multiforme (GBM)
Spread by tracking through white matter and CSF pathway
Rarely spread systemically

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6
Q

Features of meningiomas

A
Slow growing 
Extra-axial 
Usually benign 
Arise from arachnoid 
Frequently occur along the falx, convexity or sphenoid bone 
Usually cured if completely removed
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7
Q

Features of pituitary tumours

A

Adenoma most common
Only 1% will be malignant
Presents with visual disturbance due to compression of optic chiasm, and hormone imbalance

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8
Q

What percentage of cancer patients will develop cerebral metastases?

A

15-30%

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9
Q

In what percentage of cancer patients is cerebral metastases the cause of the presenting symptom?

A

15%

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10
Q

Clinical presentation of brain tumours

A

Raised ICP
Focal neurological deficit
Epileptic fits
CSF obstruction

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11
Q

Raised ICP symptoms

A
Headache (typically in morning)
Nausea/vomiting
Visual disturbance 
Somnolence 
Cognitive impairment 
Altered consciousness
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12
Q

Raised ICP signs

A
Papilloedema 
Sixth nerve palsy 
Cognitive impairment 
Altered consciousness 
Third nerve palsy
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13
Q

In what tumours does hydrocephalus occur?

A

Tumours in or close to the CSF pathway, especially in posterior fossa tumours and in children

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14
Q

How is hydrocephalus diagnosed?

A
History and examination 
CT 
MRI 
Biopsy 
Consider sources of secondary tumour
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15
Q

Lesions in what part of the brain might result in epilepsy?

A

Only in lesions above the tentorium

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16
Q

Investigations for brain tumours

A

CT
MRI
PET
Angiography

17
Q

Investigations if suspecting brain metastases

A

CT chest, abdomen and pelvis
Mammography
Biopsy skin lesion/lymph nodes

18
Q

Management goals of brain tumours

A

Accurate tissue diagnosis
Improve quality of life - decrease mass effect and improve neurological deficit
Aid effect of adjuvant therapy if required
Prolong life expectancy

19
Q

Possible managements of brain tumours

A
Corticosteroids e.g. dexamethasone 
Treat epilepsy - anticonvulsants 
Analgesics/antiemetics 
Counselling 
Surgery 
Radiotherapy 
Chemotherapy 
Endocrine replacement
20
Q

Management options for Glioblastoma multiforme

A

Complete surgical excision if possible - biopsy or debunk only
Medical - steroids, anticonvulsants
Radiotherapy
Chemotherapy - temazolamide

21
Q

Management options for brain metastases

A

Confirm diagnosis
Medical - steroids, anticonvulsants
Radiotherapy - whole brain, stereotactic
Surgery

22
Q

Prognosis of meningioma

A

Commonly cured by surgery, may require anticonvulsants

23
Q

Prognosis of astrocytomas low grade

A

Long life expectancy

24
Q

Prognosis of high grade astrocytomas/GBM

A

Average 1 year survival

25
Q

Prognosis of brain metastases

A

Frequently a good medium-term remission