Brain cancer Flashcards
What is cancer?
Disease that results when cells undergo cellular change causing proliferation and uncontrolled growth of abnormal cells.
Cells within the body, naturally go through a cellular life expectancy and death and undergo a natural process of apoptosis
Cancer cells grow uncontrollably and at different rates and do not die a natural, normal death within their life cycle.
Most tumour cells reach the brain by haematogenous spread, usually through arterial spread.
Risk factors for brain cancer
Age Gender Environmental exposures Family History Race & Ethnicity Ionizing Radiation Head trauma
Clinical signs and symptoms for brain cancer
Clinically present with: • headaches, • seizures, • mental status alterations, • ataxia, nausea & vomiting, • change in behaviour & personality and • altered visual habits.
Types of brain tumours
Cerebral Abscess, GBM, Stroke, Meningioma, Cerebral Venous Thrombosis
Pathophysiology
Within the brain, metastasis or secondary brain tumours are most commonly found in the area beneath the grey/white junction.
There are these areas classed as ‘watershed’, which are the zones on the border of major blood vessels (such as blood vessels of the COW)
Tests for brain mets
- Complete Blood Count
- Chest radiograph
- CT Brain +/- iodinated contrast
- MRI Brain
- PET Scan
- Biopsy (not usually needed if a primary cancer of another origin is known)
CT for brain mets
- Often first line of imaging for acute neurological deficits.
- Pre contrast scan will show signs of vasogenic oedema. The lesion could be isodense, hypodense or hyperdense.
- Post contrast scan will show a hypodense lesion
- Easily accessible
MRI for brain mets
Gold standard of imaging in
Brain Metastases. Replaced CT in the 1980’s.
T1, T2, FLAIR and DWI
NM for brain mets
FDG PET:
- One of the best tools for imaging metastases however can only detect mets up to 1.5cm in size.
- Lung, breast, colorectal, head and neck, melanoma and thyroid mets present usually as hypermetabolic
- Any central hypometabolism is suggestive of necrosis.
Treatment for brain mets
Corticosteroids - Corticosteroids are usually indicated in any patient with a malignant brain tumour and symptomatic peritumoral oedema. Most commonly used – Dexamethasone.
Radiotherapy – treatment of choice, WBRT.
Surgical Therapy - Surgical therapy plus post-operative WBRT is now an established treatment for patients with surgically accessible single brain metastases
Radiosurgery - Stereotactic radiosurgery is a method of delivering intense focal irradiation using a linear accelerator. Generally used on patients with lesions less than 3cm diameter.
Chemotherapy - not usually the primary therapy for most patients and is seldom the only therapy. Potentially for use for patients with small, asymptomatic tumours from primaries that are known to be chemo sensitive
What is a Glioma
Glioma is an umbrella term used to describe a group of brain tumours that arise in the glial brain cells.
Between 2007-2011 the incidence of Gliomas was 6.6 per 100,000 people with close to half of these gliomas being Glioblastomas.
Glioma encompasses:
• Astrocytomas (slow growing - usually benign)
• Oligodendrogliomas
• Oligoastrocytomas
• Glioblastoma (rapidly growing - malignant)
Glioblastoma
Most common adult primary intracranial neoplasm. Generally very aggressive and have often poor prognosis (no longer than two years normally)
Noteworthy feature of a GBM is that they can cross hemispheres using corticospinal tracts in the corpus callosum
Clinically present with focal neurological deficit, symptoms of increased intracranial pressure & seizures
Spreads quickly and invades the brain with tentacle-like projections making it harder for resection.
GBM v Glioma: A GBM is a malignant glioma, arising in the glial brain cells.
Differentials:
Metastasis, Lymphoma, Abcess, Astrocytoma, Infarction
CT for Glioblastomas
- Often first line of imaging.
- Marked mass effect
- Surrounding vasogenic oedema
- Calcification is uncommon
- Easily accessible
MRI for Glioblastomas
T1, T2, FLAIR, DWI & MR
Perfusion.
Double rim sign not visible to distinguish from an abscess.
Follow up source of imaging.
Postoperatively used in the first 24-48hrs or assess residual disease.
NM for Glioblastomas
FDG PET:
- Allows for differentiation between high and low grade tumours
- High grade demonstrate high glucose uptake
- Struggles to allow differentiation between glial and metastatic disease