Neurology Flashcards
What are the causes of primary headaches?
Migraine
Tension-type headaches
Cluster headaches
What are the causes of secondary headaches?
- Mass lesions/tumours
- Infections: meningitis, abscess, sinusitis
- Trauma: head injury or neck injury
- Raised ICP: tumour, intracranial HTN, hydrocephalus
- Decreased ICP: CSF leak, post-lumbar puncture
- Vascular: SDH, SAH, AVM, stroke, vasculitis, arterial dissection
- Metabolic: OSA, thyroid disease, B12 deficiency
- Structural abnormalities
What are the pain-sensitive structures in and around the brain?
- Large arteries at base of brain
- Meningeal arteries
- Large venous channels
- Parts of dura
- Cranial nerves V, VII, IX, X
- Skin/subcutaneous tissue, muscle, vessels, periosteum
What are the RED FLAGS in a headache history?
- First and/or worst headache
- Abrupt onset
- Change or progression of pre-existing headache pattern
- Abnormal findings on exam
- fever, stiff neck, rash
- alteration in consciousness
- focal neurological deficits - New headache in patients > 50 years
- New headache in pts with cancer, immunosuppression or pregnancy
- Headache triggered by exertion, sexual activity, Valsalva
What is the IHS criteria for migraine without aura?
A. At least 5 attacks fulfilling criteria B-D
B. Headache attacks lasting 4-72 hours (untreated or successfully treated)
C. Headache has at least 2 of the following:
- Unilateral location
- Pulsating quality
- Moderate or severe intensity
- Exacerbated by movement
D. During headache at least one of the following:
- Nausea and/or vomiting
- Photophobia and phonophobia
E. Not attributed to another disorder
What is a migraine aura?
A fully resersible set of neurological symptoms, which develop gradually over >5 minutes and last 5-60 minuts.
- visual symptoms
- sensory symptoms (paraesthesia, numbness)
- dysphasic speech disturbace
What is the IHS criteria for a tension-type headache?
A. At least 10 episodes fulfilling criteria B-D
B. Headache lasting from 30 minutes to 7 days
C. Headache has at least 2 of the following:
- Bilateral location
- Pressing/tightening (non-pulsating) quality
- Mild or moderate intensity
- Not exacerbated by movement
D. Both of the following:
- No nausea or vomiting (anorexia may occur)
- No more than one of photophobia or phonophobia
E. Not attributed to another disorder
What is the IHS criteria for a cluster headache?
A. At least 5 attacks fulfilling criteria B-D
B. Severe or very severe unilateral orbital, supraorbital and/or temporal pain lasting 15-180 minutes if untreated.
C. Headache is accompanied by at least one of the following:
- Ipsilateral conjunctival injection and/or lacrimation
- Ipsilateral nasal congestion and/or rhinorrhoea
- Ipsilateral eyelid oedema
- Ipsilateral forehead and/or facial sweating
- Ipsilateral miosis and/or ptosis
- A sense of restlessness or agitation
D. Attacks have a frequency from 1 every other day to 8 per day
E. Not attributed to another disorder
What are the differentials for acute painless loss of vision?
Central retinal artery occlusion Central retinal vein occlusion Temporal arteritis Retinal detachment Vitreous haemorrhage Exudative macular degeneration Optic neuritis
What is acute angle-closure glaucoma?
Acute angle-closure glaucoma is caused by a rapid or sudden increase in intraocular pressure (IOP), the pressure within the eye.
Patients will present with:
- acute monocular vision loss
- severe periorbital pain
- redness
- nausea and vomiting
What are the causes, presentation, examination findings and treatment for central retinal artery occlusion (CRAO)?
Cause: embolic (95%) or GCA (5%)
Presentation: profound loss of vision, instant onset (if offset, amaurosis fugax)
Examination: cloudy swelling with cherry red spot
Treatment:
- CO2 rebreathing to dilate vessel
- Acetazolamide to decrease pressure in eye
- AC paracentesis: drain fluid from eye
- ?clot lysis
What is the presentation, examinating findings and treatment of central retinal vein occlusion (CRVO)?
Presentation: sudden, painless vision loss
Risk factors: HTN, diabetes, atherosclerosis, glaucoma, smoking, CVD
Examination: ‘margherita pizza’ appearance; cotton wool spots and haemorrhage
Treatment: no acute interventions - observation + treat risk factors
What is giant cell arteritis (GCA)?
Giant cell arteritis (GCA), also called temporal arteritis, is a granulomatous vasculitis of large and medium-sized arteries. It primarily affects branches of the external carotid artery, and it is the most common form of systemic vasculitis in adults. The most common serious consequence of GCA is irreversible loss of vision due to optic nerve ischaemia.
What are the common symptoms of giant cell arteritis (GCA)?
- vision loss
- polymyalgia rheumatica
- jaw claudication
- scalp ache and tenderness
- fever
What will you find on examination of a patient with giant cell arteritis (GCA)/anterior ischaemic optic neuropathy (AION)?
- Optic disc oedema (NOT papilloedema) +/- microinfarcts, haemorrahge.
- RAPD
What is the treatment of giant cell arteritis (GCA) following presentation of acute vision loss?
It is essential to identify GCA early because it is irreversible and vision loss in the other eye is inevitable (often within 3 weeks).
MUST do these three things:
- ESR/CRP
- Steroids (i/v methylprednisolone or oral prednisolone)
- Temporal artery biopsy