Neurology Flashcards
Bell Palsy Path: Pt: Ramsay-Hunt syndrome, Bell phenomenon Dx: Tx:
Path: Idiopathic; unilateral CN VII facial nerve palsy due to inflammation or compression (lower motor neuro lesion)
Strong associated with w/ HSV
Pt:
Ipsilateral facial weakness w/ forehead involvement, drooling, loss of taste, tongue numbness, ear/retro-auricular pain
Preserved ability to raise eyebrows suggests central process (forehead innervated bilaterally)
Ramsay-Hunt syndrome: Bell’s palsy + facial varicella zoster infection
Bell phenomenon: eye on affected side moves laterally & superiorly when eye closure is attempted
No other focal neurological deficits
Dx: DOE
Tx:
Self-limiting 1 months
Prednisone: start within first 72 hrs of onset for max benefit
Artificial tears- replace lacrimation, reduce vision problems +/- eye patch/taping eye shut to sleep if severe
Acyclovir: severe cases have been shown to improve symptoms/limiting of recovery
Cerebral Aneurysm Path: Pt: Dx: Tx: Complication:
Path: Weakness in blood vessel in brain that balloons and fills w/ blood
Pt: Asx
HA, N/V, bleeding, dizziness, light sensitivity, stiff neck, thunderclap HA
Dx: MRI, MRA, CT, CTA
Tx: Supportive Embolization, endovascular coiling/clipping Antihypertensives, anticoagulants Endovascular aneurysm repair
Complications: Subarachnoid hemorrhage
Ischemic cerebral vascular accident Path: Pt: Dx: Tx:
Path: thrombosis, embolism, hypoperfusion
risks: smoking, old age, male, DM, HTN, hyperlipidemia
Pt:
Anterior:
MCA (MC): contralateral sensory/motor loss: face (eyebrows normal), and arm
ACA: contralateral sensory/motor loss: leg and foot
Posterior
PCA: visual hallucinations, contralateral homonymous hemianopsia; ipsilateral CN deficits and contralateral muscle weakness
Basilar: cerebellar dysfunction-> CN palsies, dec vision, dec bilateral sensory
Vertebral: vertigo, nystagmus, N/V, diplopia, ipsilateral ataxia
Dx: Non-con CT- loss of grey-white interface, acute hypo density (maybe normal for 1st 6-24hrs)
Tx: Thrombolytics (rTPA, alteplase)- within 3hrs of onset (some cases 4.5hrs) if no evidence of hemorrhage
Antiplatelets: ASA, clopidogrel, dipyridamole
ASA- acute setting if after 3 hrs and thrombolytics aren’t given or >/= 24 hours after thrombolytics
+/- anticoagulation- if cardio-embolic
Indications to manage HTN:
Thrombolytics > 185/110
No thrombolytics if >220/120 or MAP >/= 130
Cluster headaches Path: Pt: Dx: Tx:
Path:
Not fully understood
M > F
Pt:
Serve unilateral periorbital/temporal HA lasting <2 hrs w/ spontaneous remission
Sharp suicide HA
Attacks recur 4-8w, 1-8/day at the same time each day
Associated autonomic features (1 confirms dx) Ipsilateral Horner’s: ptosis, anhidrosis Rhinorrhea Conjunctival injection Lacrimation Aural fullness
Dx: Clx
MRI/CT- presentation consistent w/ secondary HA-> Carotid dissection, aneurism, AVMs, tumors, giant cell arthritis
Tx:
Acute- oxygen, triptans, external vagus nerve stimulation, intranasal lidocaine
Transitional (terminate daily attacks while preventive therapy is started)-> corticosteroids, prednisone taper
Glasgow coma scale (GCS)
Eye opening 'Spontaneous- 4 'Response to verbal commands- 3 'Response to pain- 2 'No eye opening- 1
Best verbal response 'Oriented- 5 'Confused- 4 'Inappropriate words- 3 'Unintelligible sounds- 2 'No verbal response- 1
Best motor response 'Obeys commands- 6 'Localizing response to pain- 5 'Withdrawal response to pain- 4 'Flexion to pain- 3 'Extension to pain- 2 'No motor response- 1
Mild brain injury >/=13
Moderate 9-12
Severe = 8
Myasthenia-Gravis Path: Pt: Dx: Tx:
Path: antibodies to acetylcholine receptors at the neuromuscular junction
Pt: ptosis, diplopia, dysphagia, dysarthria, and proximal muscle weakness
Dx:
+ tensilon test
+acetylcholine receptor binding abs
CT chest-> thymic mass
Tx: Pyridostigmine, neostigmine
steroids >60, thymectomy <60
Crisis: Plasmapheresis, IVIG
Guillain-Barre Path: Pt: Dx: Tx:
Path: Autoimmune peripheral demyelinating
Pt: Ascending paralysis following diarrhea or vaccination
Dx: intubation (if needed)
LP-> lots of protein, few cells
Best-> nerve conduction test
Tx: IVIG = plasmapheresis
NEVER give steroids!!!!
Multiple-Sclerosis Path: Pt: Dx: Tx:
Path: autoimmune central NS demyelinating
Pt: neuro sxs separated in both time and space
optic neuritis=blurry vision
Dx: MRI-> periventricular white lesions, demyelinated plaques
Tx:
acute: methylprednisolone x5 days
Chronic: interferon + glatiramer
Grand Mal Seizure Path: Pt: Dx: Tx:
Path: generalized, complex
Pt:
Convulsions = tonic clonic jerking
Loss of consciousness
Dx: EEG
Tx:Benzodiazepines
Myoclonic Seizure Path: Pt: Dx: Tx:
Path: simple, partial
Pt:
Spastic contractions
NO loss of consciousness
Dx: EEG
Tx: Valproate
Absence Seizure Path: Pt: Dx: Tx:
Path: partial, complex
Pt:
Maintains tone
Loses consciousness- 100s of times per day
Children, you think they are ADD
Dx: EEG
Tx:
Ethosuximide
Valproate
Atonic Seizure Path: Pt: Dx: Tx:
Path: Partial, simple
Pt:
Loses tone
Maintains consciousness
Dx: EEG
Tx: Valproate, helmets
Tension Headache
Path:
Pt:
Tx:
Path: Mental stress
Pt:
Bilateral, tight, band-like
No N/V or focal neurologic symptoms
Tx:
NSAIDs, aspirin, Tylenol
TCAs in severe recurrent cases
PPX: beta blockers
Cluster Headache
Pt:
Dx:
Tx:
Pt: Serve unilateral periorbital/temporal HA lasting <2 hrs w/ spontaneous remission
Sharp suicide HA
Attacks recur 4-8w, 1-8/day at the same time each day
Associated autonomic features (1 confirms dx)
Ipsilateral Horner’s: ptosis, anhidrosis
Rhinorrhea
Conjunctival injection
Lacrimation
Aural fullness
Dx:
Clx
MRI/CT- presentation consistent w/ secondary HA
Carotid dissection, aneurism, AVMs, tumors, giant cell arthritis
Tx:
Acute- oxygen, triptans, external vagus nerve stimulation, intranasal lidocaine
Transitional (terminate daily attacks while preventive therapy is started)-> corticosteroids, prednisone taper
ppx: verapamil, lithium, valproate
Migraines
Pt:
Tx:
Pt: pulsing, unilateral, nausea, disabling, aggravated by physical activity, typically associated w/ photophobia
Tx: triptans
ppx: MgO, B2, coenzyme Q10, TCA/SSRI