Neurological tumours Flashcards
- The most common childhood brain tumour.
- Well circumscribed
- Most often in posterior fossa
Pilocytic astrocytoma
The most common malignant childhood brain tumour
Medulloblastoma
Medulloblastoma most commonly affects the ______ and can cause compression of ______
Cerebellum
4th ventricle (causing hydrocephalis)
Can also cause truncal ataxia (cebrellar vermis) + drop mets to the spinal cord
Ependymoma most commonly affects ______ and causes ______
4th ventricle
Hydrocephalus
________ is the most common chilhood supratentorial tumour
Craniopharyngioma
What childhood tumour is associated with calcification, bitemporal hemianopia + high recurrence rate
Craniopharyngioma
Perinaud syndrome describes what features in _______ tumours?
In pineal tumours:
- Upward/ vertical gaze palsy
- convergence-retraction nystagmus
- light-near dissociation
- Ataxia
__________ is the most common, malignant brain tumour in adults
Glioblastoma (grade IV astrocytoma)
Glioblastoma gross anatomical features
Can cross corpus callosum
In cerebral hemispheres
- Often affects the frontal lobes
- Rare, slow growing
- Calcified
Oligodendrocytes
- Females > Males
- Extra-axial tumour
- Can present with seizure/ focal neurology
Meningioma
Most common cerebellar in adults
Associated with von Hippel-Lindau syndrome
Hemangioblastoma
What brain tumour can cause secondary polycythema secondary to EPO production
Hemangioblastoma
Associated with neurofibrosis type 2 when bilateral
Schwannomas
Schwannomas commonly affect what nerves
Cranial nerve 5, 7, 8
Peripheral nerves
Can present with hearing loss and tinnitus
Often localised to the internal acoustic meatus
Schwannoma
First line treatment for prolactinoma
Dopamine agonist
- Cabergoline
- Bromocroptine
Disconnection hyperprolactinoma
Infundobulat stalk damage
- inhibits hypothalamic dopamine effect on pituitary lactotrophs (i.e. tumour with suprasellar extension, trauma, surgery)
Management- surgery
Treatment of acoustic neuromas
Significant hearing loss/ large tumour- surgical resection/ radiation
Small tumour/ minimal hearing loss/ very old age- MRI surveillance 6-12 months
Treatment of acromegaly
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
Follow up after treatment of acromegaly
IGF-1 and GH levels 12 weeks post-surgery, then annnually
Annual hormone testing for hypopituitrism
MRI 12-weeks post-surgery
Complications of acromeagly
CVD- main cause of death
- HTN, LVH, cardiomyopathy
Diabetes
Colon polyps/ cancer
Thyroid cancer/ enlargement
Carpal tunnel
Cerebral aneurysm
Hypopituitarism