Neurological tumours Flashcards

1
Q
  • The most common childhood brain tumour.
  • Well circumscribed
  • Most often in posterior fossa
A

Pilocytic astrocytoma

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2
Q

The most common malignant childhood brain tumour

A

Medulloblastoma

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3
Q

Medulloblastoma most commonly affects the ______ and can cause compression of ______

A

Cerebellum
4th ventricle (causing hydrocephalis)

Can also cause truncal ataxia (cebrellar vermis) + drop mets to the spinal cord

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4
Q

Ependymoma most commonly affects ______ and causes ______

A

4th ventricle
Hydrocephalus

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5
Q

________ is the most common chilhood supratentorial tumour

A

Craniopharyngioma

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6
Q

What childhood tumour is associated with calcification, bitemporal hemianopia + high recurrence rate

A

Craniopharyngioma

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7
Q

Perinaud syndrome describes what features in _______ tumours?

A

In pineal tumours:
- Upward/ vertical gaze palsy
- convergence-retraction nystagmus
- light-near dissociation
- Ataxia

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8
Q

__________ is the most common, malignant brain tumour in adults

A

Glioblastoma (grade IV astrocytoma)

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9
Q

Glioblastoma gross anatomical features

A

Can cross corpus callosum

In cerebral hemispheres

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10
Q
  • Often affects the frontal lobes
  • Rare, slow growing
  • Calcified
A

Oligodendrocytes

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11
Q
  • Females > Males
  • Extra-axial tumour
  • Can present with seizure/ focal neurology
A

Meningioma

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12
Q

Most common cerebellar in adults

Associated with von Hippel-Lindau syndrome

A

Hemangioblastoma

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13
Q

What brain tumour can cause secondary polycythema secondary to EPO production

A

Hemangioblastoma

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14
Q

Associated with neurofibrosis type 2 when bilateral

A

Schwannomas

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15
Q

Schwannomas commonly affect what nerves

A

Cranial nerve 5, 7, 8
Peripheral nerves

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16
Q

Can present with hearing loss and tinnitus

Often localised to the internal acoustic meatus

A

Schwannoma

17
Q

First line treatment for prolactinoma

A

Dopamine agonist
- Cabergoline
- Bromocroptine

18
Q

Disconnection hyperprolactinoma

A

Infundobulat stalk damage
- inhibits hypothalamic dopamine effect on pituitary lactotrophs (i.e. tumour with suprasellar extension, trauma, surgery)

Management- surgery

19
Q

Treatment of acoustic neuromas

A

Significant hearing loss/ large tumour- surgical resection/ radiation

Small tumour/ minimal hearing loss/ very old age- MRI surveillance 6-12 months

20
Q

Treatment of acromegaly

A

1st line- surgery
- Transsphenoidal adenomectomy
- parasellar/ inoperable disease= surgical debulking

Inoperable/ unsuccessful tumour- medication/ radiotherapy
- somatostatin analogues- ocreotide, lanreotide
- dopamine agonist
- GH receptor antagonist= pegvisomant

21
Q

Follow up after treatment of acromegaly

A

IGF-1 and GH levels 12 weeks post-surgery, then annnually

Annual hormone testing for hypopituitrism

MRI 12-weeks post-surgery

22
Q

Complications of acromeagly

A

CVD- main cause of death
- HTN, LVH, cardiomyopathy

Diabetes

Colon polyps/ cancer

Thyroid cancer/ enlargement

Carpal tunnel

Cerebral aneurysm

Hypopituitarism

23
Q
A