Central Nervous System (CNS) Tumours Flashcards

1
Q

What are the types of CNS tumours

A

=> tumours of neuroepithelial tissue

  • Astrocytoma
  • Oligodendroglioma

=> Tumours of the nerve sheath
- Schwannoma
Neurofibroma

  • Lymphoma

=>Germ cell tumours

  • Germinoma
  • Teratoma

=> sellar region

  • Pituitary adenoma
  • Craniopharyngioma

=>Meningiomas

=>Metastases

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2
Q

What is the most common cause of a CNS tumour

A

Metastases

Often from: 
LUNG
BREAST
Kidney 
Stomach 
Colon 
Melanoma
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3
Q

What CNS tumours are the most common primary brain tumour and benign tumour

A

Primary tumour - astrocytoma

Benign tumours - meningioma and acoustic neuroma

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4
Q

General symptoms of a CNS tumour

A

Raised ICP headache (worse on waking up, lying down, leaning forward + morning nausea)
Nausea and vomiting
FLAWS
Symptoms of area compression

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5
Q

General signs of CNS tumours on examination

A

Papilloedema on fundoscopy (Raised ICP)

Cushing’s reflex: bradycardia, hypertension, irregular breathing

Vestibular schwannoma - loss of corneal reflex

Bitemporal hemianopia: craniopharyngioma + pituitary adenoma

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6
Q

Describe astrocytomas (aetiology + signs)

A

Can form glioblastoma multiforme (GMB), the most common primary brain tumour

Signs - Focal neurological deficits according to location (e.g., frontal, temporal, cerebellum, brainstem) or with signs of elevated intracranial pressure

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7
Q

Describe Oligodendroglioma (aetiology)

A

Slow-growing, defined tumour originating from oligodendrocytes
Common in frontal lobes

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8
Q

Describe schwannomas (aetiology + symptoms + signs)

A

Non-invasive and slow-growing tumour of schwann cells that surround cranial nerve roots/peripheral nerves

Vestibular schwannoma/acoustic neuroma = tumour from CNVIII = loss of corneal reflex
+ Hearing loss
+ Facial paralysis
+ Tinnitus

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9
Q

Describe neurofibroma (aetiology)

A

Originate from Schwann cells, fibroblasts or perineural-like cells
Higher risk of malignancy than schwannomas
Involve spinal nerve roots or peripheral nerve

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10
Q

Describe CNS lymphomas (aetiology + signs)

A

Forms around periventricular parenchymal blood vessels
Solitary or multifocal
Generally in immunocompromised patients
Associated with EBV infection in HIV +ve patients

Signs: lymphadenopathy

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11
Q

Describe the germ cell tumours of the CNS

A

Germinoma: primitive spheroidal cell tumour

Teratoma: contains a mixture of well differentiated tissues originating from the germ cell layers -> forms dermis, muscle, bone, teeth, hair etc.

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12
Q

Describe Craniopharyngioma

A

Most common paediatric supratentorial tumour

Solid/cystic tumour of the sella region, derived from the remnants of Rathke’s pouch

Symptoms:
Hormonal disturbance
Hydrocephalus

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13
Q

Describe meningiomas (aetiology + symptoms)

A

Second most common primary brain tumour
Typically benign tumours that arise from the dura mater of the meninges

Symptoms:
Neurological deficit + progressive, focal or general headaches

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14
Q

Investigations for CNS tumours

A

Gadolinium-enhanced MRI: preferred initial investigations - shows hypointense on T1 or hyperintense on T2
Biopsy: confirms type of tumour

Pituitary function tests: If pituitary tumour/craniopharyngioma is suspected

CT head: detects 90%
CT CAP/CXR/PET: mets

EEG: evaluate functional changes
CSF analysis: (LP often CI)

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