CNS Flashcards
What are the two most common CNS tumours?
known as primitive neuroectodermal tumours
- pinealoblastoma
- medulloblastoma
What is the metastasis of PNET?
- highly invasive
- spread rapidly through CSF
- 20% have spread to SC before diagnosis
Where do medulloblastomas arise?
- in cerebrellum or posterior fossa
What is the most common and rare type of PNET?
Common - medulloblastoma (20% of all paediatric brain tumours)
Rare - pinealoblastoma
What is the epidemiology of medulloblastoma?
- rare in adults: most occur before 16
- more common in males (M:F, 2:1)
What causes the signs and symptoms for PNET?
- associated with raised intracranial pressure which can be caused by a blockage of the ventricles leading to a build up of CSF
- local swelling around the tumour itself
What are the signs and symptoms of medulloblastoma?
- headache
- vomiting
- irritability
- problems with motor function
What are the signs and symptoms of glioblastoma?
- headaches
- seizures
- vomitting
- trouble speaking
- blurred vision
What classifies an average risk patient?
- older then 3
- minimal or no residual tumour (<1.5cm max diameter)
- no evidence of metastatic spread
What classifies a high risk patient
- significant residual disease (>1.5cm max diameter)
- evidence of metastatic disease
- under 3
What are the three main treatment modalities for PNET?
- surgery
- craniospinal irradiation
- adjuvant chemotherapy
When is surgery used for PNET?
- essential as first line treatment
- should be as complete as possible without causing disability
How soon after surgery should CNS RT commence?
- as soon as recovery permits (2-3 weeks) because of risk of tumour seeding
- post foassa or primary tumour site to be boosted after whole CNS treatment
When should chemo be used?
- concurrent chemo followed by adjuvant mutli agent therapy for 1 year has proven improved survival
If child is under 3 is RT used?
- usually delayed because of associated risks, but control rates are higher when radiation is used