Central Nervous System (CNS) Tumours Flashcards
What are the types of CNS tumours
=> 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
What is the most common cause of a CNS tumour
Metastases
Often from: LUNG BREAST Kidney Stomach Colon Melanoma
What CNS tumours are the most common primary brain tumour and benign tumour
Primary tumour - astrocytoma
Benign tumours - meningioma and acoustic neuroma
General symptoms of a CNS tumour
Raised ICP headache (worse on waking up, lying down, leaning forward + morning nausea)
Nausea and vomiting
FLAWS
Symptoms of area compression
General signs of CNS tumours on examination
Papilloedema on fundoscopy (Raised ICP)
Cushing’s reflex: bradycardia, hypertension, irregular breathing
Vestibular schwannoma - loss of corneal reflex
Bitemporal hemianopia: craniopharyngioma + pituitary adenoma
Describe astrocytomas (aetiology + signs)
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
Describe Oligodendroglioma (aetiology)
Slow-growing, defined tumour originating from oligodendrocytes
Common in frontal lobes
Describe schwannomas (aetiology + symptoms + signs)
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
Describe neurofibroma (aetiology)
Originate from Schwann cells, fibroblasts or perineural-like cells
Higher risk of malignancy than schwannomas
Involve spinal nerve roots or peripheral nerve
Describe CNS lymphomas (aetiology + signs)
Forms around periventricular parenchymal blood vessels
Solitary or multifocal
Generally in immunocompromised patients
Associated with EBV infection in HIV +ve patients
Signs: lymphadenopathy
Describe the germ cell tumours of the CNS
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.
Describe Craniopharyngioma
Most common paediatric supratentorial tumour
Solid/cystic tumour of the sella region, derived from the remnants of Rathke’s pouch
Symptoms:
Hormonal disturbance
Hydrocephalus
Describe meningiomas (aetiology + symptoms)
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
Investigations for CNS tumours
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)