Neurology: Oncology and Hydrocephalus
🧭 This chapter brings together brain tumours and hydrocephalus. Acute spinal cord compression, meningitis and encephalitis are covered in the Neurological Emergencies chapter.
Your four questions for every patient: Is there a structural cause that needs imaging? Is this a treatable complication of a systemic disease, drug or infection? Is the problem functional - and have I made a positive diagnosis rather than just excluding things? What does the patient need to know about driving and safety?
Brain Tumours
Types:
- Metastases - the commonest brain tumours in adults. They come from the lung (the commonest), breast, melanoma, kidney and colon. Often multiple, at the grey–white matter junction.
- Gliomas (WHO 2021 classification uses molecular markers):
- Glioblastoma (IDH-wildtype) - the commonest primary malignant tumour; older adults; aggressive. MRI with contrast. Glioblastoma shows ring enhancement with central necrosis and surrounding oedema.
- Astrocytoma, IDH-mutant - younger adults; slower.
- Oligodendroglioma (IDH-mutant, 1p/19q codeleted) - often presents with seizures; best prognosis of the gliomas; often calcified.
Meningioma: The commonest primary brain tumour overall - usually benign, slow-growing, arising from the meninges. Commoner in women; after radiation; in NF2. Often found by chance. Meningioma MRI with contrast shows a dural-based enhancing mass with a "dural tail"
Primary CNS lymphoma: Immunosuppressed people (HIV, transplant) and older adults. Deep periventricular lesions. Avoid steroids before biopsy if possible - they can make the lymphoma disappear temporarily and prevent diagnosis.
Others:
- Vestibular schwannoma (acoustic neuroma) - one-sided hearing loss, tinnitus, imbalance.
- Pituitary tumours (see the Pituitary chapter).
- Craniopharyngioma.
- Haemangioblastoma (VHL).
- Children: medulloblastoma, pilocytic astrocytoma, ependymoma (posterior fossa).
How brain tumours present:
- Seizures - especially low-grade gliomas and meningiomas. A new seizure in an adult always needs brain imaging.
- Progressive focal deficit - weakness, speech or visual field loss developing over weeks.
- Cognitive or personality change (frontal tumours) - can be mistaken for depression or dementia.
- Raised intracranial pressure: Headache worse on lying down, coughing and in the morning. Vomiting. Papilloedema. Sixth nerve palsy. Drowsiness.
- Headache alone is an uncommon presentation.
Referral (NICE NG12): Adults with progressive, subacute loss of central neurological function should have an urgent direct-access MRI (or CT) or suspected cancer referral.
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Managing Brain Tumours
- Imaging: MRI with contrast. Glioblastoma shows ring enhancement with central necrosis and surrounding oedema; meningioma shows a dural-based enhancing mass with a "dural tail".
- Differential diagnosis of a ring-enhancing lesion:
- Glioblastoma.
- Metastasis.
- Abscess.
- Toxoplasmosis (HIV).
- Lymphoma.
- Tumefactive demyelination.
- Radiation necrosis.
- Symptom control:
- Dexamethasone for symptomatic brain swelling (e.g. 8–16 mg daily, then reduce to the lowest effective dose). Give a PPI, monitor glucose, and watch for steroid myopathy, infection and mood change. Give in the morning.
- Seizures: Levetiracetam (few interactions with chemotherapy). No routine prevention without seizures.
- VTE is common - prophylaxis and treatment as appropriate.
- Glioblastoma (NICE NG99):
- Maximal safe surgical resection, then radiotherapy with temozolomide, then 6 cycles of temozolomide.
- MGMT promoter methylation predicts better response to temozolomide.
- Median survival about 12–18 months.
- Shorter radiotherapy courses for older or frailer patients.
- Lower-grade gliomas: Surgery, radiotherapy and chemotherapy (PCV or temozolomide). IDH inhibitors (e.g. vorasidenib) are a newer option for some IDH-mutant tumours.
- Meningioma: Watch-and-scan if small and without symptoms; surgery or stereotactic radiosurgery if growing or symptomatic.
- Brain metastases:
- Stereotactic radiosurgery for a limited number of lesions; surgery for a single large lesion.
- Systemic therapies that cross into the brain (e.g. targeted drugs in lung cancer and melanoma).
- Whole-brain radiotherapy is now used less often.
- Best supportive care for poor performance status.
- Holistic care:
- Clinical nurse specialist.
- Rehabilitation.
- Cognitive and mood support.
- Driving (DVLA rules depend on tumour type and treatment).
- Early palliative care and advance care planning.
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Paraneoplastic Neurological Syndromes
What they are: Immune attacks on the nervous system triggered by a cancer elsewhere. They often appear before the cancer is found, develop over weeks, and can be very disabling.
| Syndrome | Typical antibody and cancer |
| Lambert–Eaton syndrome | VGCC - small cell lung cancer |
| Subacute cerebellar degeneration | Anti-Yo (ovary, breast); anti-Tr (Hodgkin lymphoma); anti-Hu |
| Limbic encephalitis | Anti-Hu (small cell lung cancer); anti-Ma2 (testicular cancer); anti-AMPA, GABA-B |
| Sensory neuronopathy | Anti-Hu - small cell lung cancer |
| Opsoclonus–myoclonus | Anti-Ri (breast); neuroblastoma in children |
| Stiff person syndrome | Anti-amphiphysin (breast); anti-GAD (usually not paraneoplastic - associated with type 1 diabetes) |
| Anti-NMDA receptor encephalitis | Ovarian teratoma |
- Search for the cancer: CT chest, abdomen and pelvis; PET-CT; mammography, testicular or pelvic ultrasound as relevant. Repeat for up to 2–4 years if negative.
- Treatment: Treat the cancer - the most important step. Add immunotherapy (steroids, IVIg, plasma exchange, rituximab); syndromes with antibodies to intracellular targets (Hu, Yo) respond poorly.
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Hydrocephalus and Normal Pressure Hydrocephalus
- Hydrocephalus: Enlarged ventricles from blocked or poorly absorbed CSF.
- Obstructive (non-communicating) - tumour, aqueduct stenosis, colloid cyst, posterior fossa haemorrhage.
- Communicating - after subarachnoid haemorrhage, meningitis or head injury (absorption blocked).
- Acute hydrocephalus causes headache, vomiting, drowsiness and upgaze palsy - neurosurgical emergency (external ventricular drain).
- Normal pressure hydrocephalus (NPH):
- Older adults; often idiopathic, or after SAH, meningitis or head injury.
- Classic triad:
- Gait disturbance first - broad-based, shuffling, "magnetic" gait with difficulty turning.
- Urinary urgency and incontinence.
- Cognitive slowing (frontal-subcortical).
- Imaging: Enlarged ventricles out of proportion to atrophy (Evans index over 0.3), with tight high-convexity sulci.
- Tap test: Remove 30–50 mL of CSF by LP and re-test gait, or use a lumbar drain for several days. Improvement predicts benefit from a shunt.
- Treatment: Ventriculoperitoneal shunt. Gait responds best; cognition responds least.
- Mimics: vascular parkinsonism, Parkinson's disease, cervical myelopathy, Alzheimer's disease.
- Shunt problems:
- Blockage - headache, vomiting, drowsiness (raised pressure) - urgent neurosurgical review.
- Infection - often within months of surgery (staphylococci).
- Over-drainage - low-pressure headache, subdural collections.
Drug Reference Table
| Drug | Key points |
Dexamethasone
e.g. 8–16 mg daily, then reduce | Brain tumour oedema; give with a PPI; check glucose; avoid before biopsy if lymphoma is suspected. |
| Levetiracetam | Seizures with brain tumours; few interactions. |
| Temozolomide | Glioblastoma with radiotherapy; myelosuppression; better response if MGMT is methylated. |
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Spot the Diagnosis
| Clue | Diagnosis |
| Ring-enhancing lesion with central necrosis and oedema in a 68-year-old | Glioblastoma (or metastasis) |
| Dural-based enhancing mass with a dural tail | Meningioma |
| Deep periventricular lesion that shrank after steroids in a transplant recipient | Primary CNS lymphoma |
| Rapid unsteadiness in a woman, anti-Yo antibodies | Paraneoplastic cerebellar degeneration (ovarian or breast cancer) |
| Shuffling magnetic gait, incontinence and slowed thinking, big ventricles | Normal pressure hydrocephalus |
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Exam-style Scenarios
1. A 62-year-old has had 6 weeks of worsening left arm weakness and personality change. MRI shows a right frontal ring-enhancing mass with oedema.
Answer: Likely glioblastoma (or metastasis).
- Dexamethasone with a PPI; glucose checks.
- CT chest, abdomen and pelvis to look for a primary.
- Neuro-oncology MDT: maximal safe resection, then radiotherapy with temozolomide.
- Seizure plan; DVLA advice; specialist nurse and palliative care.
2. A 75-year-old has 1 year of a shuffling gait, then urinary urgency and slowed thinking. CT shows enlarged ventricles.
Answer: Suspected normal pressure hydrocephalus.
- CSF tap test (or lumbar drain) with gait assessment before and after.
- Refer to neurosurgery for a VP shunt if he improves.
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Key Points
- Metastases are the commonest brain tumours; glioblastoma is the commonest primary malignant one; meningioma is the commonest primary overall.
- A new seizure or a progressive focal deficit in an adult needs brain imaging.
- Dexamethasone for tumour oedema (with PPI and glucose checks); avoid steroids before biopsy if lymphoma is likely.
- Glioblastoma: surgery, radiotherapy and temozolomide; MGMT methylation predicts response.
- Paraneoplastic syndromes often come before the cancer - search with CT and PET.
- NPH: gait, incontinence, cognition - tap test, then shunt.
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Guidelines and Further Reading
- NICE NG99: Brain tumours (primary) and brain metastases in over 16s
- NICE NG12: Suspected cancer - recognition and referral
- WHO Classification of Tumours of the Central Nervous System (2021)
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