Brain metastases (N) Flashcards

1
Q

What are brain metastases the most common cause of?

A

Metastatic brain cancer is the most common form of brain tumours in adults

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2
Q

Which cancers most commonly metastasise to the brain? (6)

A
  • lung (most common)
  • breast
  • colorectal
  • testicular
  • skin (melanoma)
  • kidney
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3
Q

What are the clinical features of brain metastases? (5)

A
  • persistent headaches - worse in mornings and when lying down (suggests raised ICP)
  • seizures
  • focal neurological deficits (e.g. changes in speech, vision, hearing)
  • cognitive deficits
  • CN VI palsy (medially diverted eye) and diplopia may be first presentation
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4
Q

What is the first-line investigation for brain metastases?

A

Imaging (CT/MRI) - can see well-circumscribed tumours at junction of grey and white matter

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5
Q

What imaging do you do for progressively worsening headache with higher cognitive function impaired?

A

Brain MRI over CT as you can see more detail of brain anatomy

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6
Q

What is the first-line management for brain metastases?

A

High-dose dexamethasone (reduces cerebral oedema)

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7
Q

How do we manage limited brain metastases?

A

Surgical resection

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8
Q

What management options do we have for extensive brain metastases? (3)

A
  • stereotactic radiosurgery
  • whole brain radiation therapy
  • chemotherapy
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9
Q

Describe the prognosis of brain metastases.

A

Mean survival approximately 1 month without treatment and <1 year with treatment

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10
Q

Describe glioblastoma multiforme. (5)

A
  • glioblastoma is the most common primary tumour in adults associated with poor prognosis (~1y)
  • Ix - imaging: solid tumours with central necrosis and a rim that enhances with contrast
  • disruption of BBB - associated with vasogenic oedema
  • histology: pleomorphic tumour cells border necrotic areas
  • Rx: surgical with postoperative chemo and/or radiotherapy; dexamethasone for cerebral oedema
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11
Q

Describe meningioma. (7)

A
  • second most common primary brain tumour in adults (after glioblastoma)
  • typically benign, extrinsic tumours of CNS
  • arise from arachnoid cap cells of the meninges and are typically located next to the dura and cause Sx by compression rather than invasion
  • typically located at falx cerebri, superior sagittal sinus, convexity or skull base
  • histology: spindle cells in concentric whorls and calcified psammoma bodies
  • Ix: CT (will show contrast enhancement) and MRI
  • Rx: observation, radiotherapy or surgical resection
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12
Q

Describe vestibular schwannoma. (6)

A
  • benign tumour arising from CN VIII (vestibulocochlear nerve)
  • Sx: hearing loss, facial nerve palsy (compression) and tinnitus
  • neurofibromatosis type 2 associated with bilateral vestibular schwannomas
  • histology: Antoni A or B patterns seen
  • Verocay bodies (acellular areas surrounded by nuclear palisades)
  • Rx: observation, radiotherapy or surgery
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13
Q

Describe pilocytic astrocytoma.

A
  • most common primary brain tumour in children
  • histology: Rosenthal fibres (corkscrew eosinophilic bundle)
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14
Q

Describe medulloblastoma. (4)

A
  • aggressive paediatric brain tumour that arises within the infratentorial compartment
  • spreads through CSF system
  • histology: small, blue cells; rosette pattern of cells with many mitotic features
  • Rx: surgical resection and chemotherapy
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15
Q

Describe ependymoma. (3)

A
  • commonly seen in 4th ventricle
  • may cause hydrocephalus
  • histology: perivascular pseudo-rosettes
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16
Q

Describe oligodendroma. (2)

A
  • benign, slow-growing tumour common in frontal lobes
  • histology: calcifications with ‘fried-egg’ appearance
17
Q

Describe hemangioblastoma. (3)

A
  • vascular tumour of cerebellum
  • associated with von Hippel-Lindau syndrome
  • histology: foam cells and high vascularity
18
Q

Describe pituitary adenoma. (7)

A
  • benign tumours of pituitary gland
  • secretory (produce hormone in excess) or non-secretory
  • divided into microadenomas (<1cm) or macroadenomas (>1cm)
  • Sx: consequences of hormone excess (e.g. Cushing’s due to ACTH, or acromegaly due to GH) or depletion
  • compression of optic chiasm –> bitemporal hemianopia due to crossing nasal fibres
  • Ix: pituitary blood profile + MRI
  • Rx: hormonal or surgical (e.g. transphenoidal resection)
19
Q

Describe craniopharyngioma. (7)

A
  • most common paediatric supratentorial tumour
  • solid/cystic tumour of the sellar region that is derived from remnants of Rathke’s pouch
  • common in children, but can also present in adults
  • Sx: may present with hormonal disturbance, Sx of hydrocephalus or bitemporal hemianopia
  • histology: derived from remnants of Rathke’s pouch
  • Ix: pituitary blood profile + MRI
  • Rx: usually surgical +/- postoperative radiotherapy