Master Neurology
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Core Concepts
Neurology focuses on diseases of the central (brain, spinal cord) and peripheral (nerves, muscles, neuromuscular junction) nervous systems. Key to diagnosis is anatomical localisation of lesions and understanding the pathophysiological process. Common presentations include weakness, sensory disturbances, abnormal movements, headaches, seizures, and cognitive impairment. The cranial nerves, sensory tracts (spinothalamic, posterior column), and motor tracts (corticospinal) are fundamental for localisation.
Clinical Presentation
- Stroke/TIA: Acute onset focal neurological deficit (e.g., hemiparesis, dysphasia, visual field loss). TIA symptoms resolve within 24 hours.
- Seizures: Transient disturbance of brain function due to abnormal electrical activity. Can be generalised (e.g., tonic-clonic, absence) or focal (with or without impaired awareness).
- Multiple Sclerosis (MS): Relapsing-remitting episodes of neurological dysfunction (e.g., optic neuritis, sensory symptoms, weakness, ataxia), separated in time and space.
- Parkinson's Disease: Bradykinesia, rigidity (cogwheel), resting tremor (pill-rolling), postural instability.
- Myasthenia Gravis: Fluctuating fatigable weakness, worse with exertion, better with rest. Affects ocular muscles (ptosis, diplopia), bulbar muscles (dysphagia, dysarthria), and limbs.
- Guillain-BarrΓ© Syndrome (GBS): Rapidly progressive, ascending flaccid paralysis with areflexia, often preceded by infection. Risk of respiratory failure.
- Motor Neuron Disease (MND/ALS): Progressive weakness with signs of both upper (spasticity, brisk reflexes) and lower (fasciculations, wasting) motor neuron involvement, typically without sensory loss.
- Headaches:
- Migraine: Unilateral, pulsatile, moderate-severe, photophobia/phonophobia, aura.
- Tension: Bilateral, band-like, mild-moderate, no severe associated symptoms.
- Cluster: Unilateral, excruciating periorbital pain, associated with ipsilateral autonomic features (lacrimation, ptosis, rhinorrhoea).
- Dementia: Progressive decline in memory and other cognitive functions (e.g., language, executive function, visuospatial skills) severe enough to interfere with daily life.
Diagnosis (Gold Standard)
Stroke: Immediate CT brain to rule out haemorrhage. MRI brain (DWI sequence) for acute ischemia. Carotid Doppler for TIA/ischemic stroke workup.
Seizures: Clinical diagnosis, EEG (epileptiform activity), MRI brain to exclude structural lesions.
MS: MRI brain and spinal cord (dissemination in space and time per McDonald criteria), CSF oligoclonal bands.
Parkinson's Disease: Clinical diagnosis based on UK Brain Bank criteria. DAT scan can aid differentiation from essential tremor.
Myasthenia Gravis: Acetylcholine receptor antibodies (most common), MuSK antibodies. EMG (decremental response to repetitive nerve stimulation).
GBS: Clinical criteria, CSF (albumino-cytological dissociation), NCS/EMG (demyelinating features).
MND: Clinical diagnosis (El Escorial criteria), EMG (denervation/reinnervation).
Headaches: Clinical (International Headache Society criteria). MRI for red flags.
Dementia: Clinical history, cognitive screening (MMSE, MoCA), MRI brain (atrophy, vascular changes, rule out reversible causes).
Management (First Line)
Ischemic Stroke: IV thrombolysis (alteplase within 4.5h), mechanical thrombectomy (within 6-24h for large vessel occlusion). Antiplatelets (aspirin), statins, blood pressure control, rehabilitation.
Haemorrhagic Stroke: Blood pressure control, neurosurgical consultation for evacuation in selected cases.
Acute Seizures: IV lorazepam/diazepam. Status epilepticus: IV benzodiazepines, then phenytoin/levetiracetam/valproate.
Long-term Seizure: Antiepileptic drugs (e.g., lamotrigine, levetiracetam, carbamazepine, valproate) based on seizure type and patient factors.
Parkinson's Disease: Levodopa (most effective), dopamine agonists (e.g., ropinirole), MAO-B inhibitors (e.g., rasagiline).
MS Relapse: High-dose IV corticosteroids (methylprednisolone). Disease-modifying therapies (DMTs) for long-term management (e.g., interferon-beta, glatiramer acetate, natalizumab, ocrelizumab).
Myasthenia Gravis: Pyridostigmine (symptomatic). Immunosuppression (steroids, azathioprine). Crisis: IVIG or plasmapheresis.
GBS: IVIG or plasmapheresis. Supportive care, including respiratory support.
MND: Riluzole (slows progression). Symptomatic management (e.g., baclofen for spasticity, non-invasive ventilation).
Migraine: Acute: NSAIDs, triptans. Prophylaxis: Beta-blockers (propranolol), topiramate, amitriptyline.
Cluster Headache: Acute: High-flow oxygen, sumatriptan SC. Prophylaxis: Verapamil.
Alzheimer's Dementia: Cholinesterase inhibitors (donepezil, rivastigmine, galantamine) for mild-moderate. Memantine for moderate-severe.
Exam Red Flags
- Thunderclap headache: Sudden, severe headache reaching maximal intensity in seconds. Consider Subarachnoid Haemorrhage (SAH) β urgent CT head.
- Headache with papilloedema: Raised intracranial pressure (e.g., brain tumour, idiopathic intracranial hypertension, cerebral venous thrombosis).
- Fever, headache, neck stiffness, photophobia: Meningitis/Encephalitis β urgent LP after CT head (if indicated).
- New-onset focal neurological deficit (acute): Stroke/TIA.
- Acute painful vision loss in elderly with jaw claudication: Giant Cell Arteritis β urgent ESR/CRP and steroid treatment.
- New onset seizure in adult: Rule out structural causes (e.g., tumour, stroke) with MRI brain.
- Progressive weakness with respiratory compromise: Myasthenic crisis, GBS, MND β requires urgent airway assessment.
- Unexplained gait disturbance, urinary incontinence, dementia: Normal Pressure Hydrocephalus.
Sample Practice Questions
A 28-year-old woman presents with a 3-day history of gradually worsening double vision and drooping of her left eyelid, which is worse in the evenings and improves significantly after rest. She occasionally experiences difficulty swallowing and complains of generalised fatigue. There is no sensory loss or pain. On examination, she has partial ptosis of the left eyelid and limited abduction of the left eye. Her pupils are equal and reactive. Muscle strength in her limbs appears normal at rest, but after sustained effort (e.g., repeatedly clenching her fists), she develops mild weakness.
A 58-year-old woman presents with gradually progressive difficulty walking over the past year. She describes stiffness and slowness of movement, and her family has noticed a reduced facial expression and a tremor in her right hand at rest. On examination, she has a stooped posture, bradykinesia, cogwheel rigidity, and a resting tremor. Her cognition is intact. What is the most likely diagnosis?
A 72-year-old woman develops sudden onset of 'the worst headache of her life', accompanied by neck stiffness, photophobia, and nausea. She has no focal neurological deficits. Her blood pressure is 160/90 mmHg. What is the most appropriate diagnostic investigation?
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