Iran Specialty Board Neurology flashcards
Iran Specialty Board Neurology · Build recall with a focused review session.
36 cards. Read the term and the definition here. The deck at the top of this page is optional.
- DWI-FLAIR mismatch
- In wake-up stroke, restricted diffusion on DWI without FLAIR hyperintensity indicates onset within about 4.5 hours, supporting intravenous thrombolysis when other criteria are met.
- Spot sign
- Contrast extravasation on CT angiography within an intracerebral hematoma predicts hematoma expansion and worse outcome, prompting aggressive blood pressure control and reversal of anticoagulation.
- Xanthochromia
- Yellowish CSF supernatant from bilirubin breakdown, appearing about 12 hours after subarachnoid hemorrhage; it distinguishes true hemorrhage from traumatic lumbar puncture.
- NIHSS large-vessel occlusion clue
- A score of 6 or more with cortical signs such as gaze deviation, aphasia, or neglect suggests large-vessel occlusion and warrants immediate CT angiography for thrombectomy evaluation.
- Status epilepticus definition
- Continuous seizure activity or recurrent seizures without recovery lasting 5 minutes or more, requiring immediate benzodiazepines followed by a second-line antiepileptic loading dose.
- Juvenile myoclonic epilepsy
- Generalized epilepsy with morning myoclonic jerks, 3-4 Hz polyspike-wave discharges, and photosensitivity; valproate is highly effective but avoided in women of childbearing potential.
- Breach rhythm
- A benign EEG variant over a skull defect with faster, higher-amplitude activity; it must not be misinterpreted as an epileptiform discharge or seizure pattern.
- SUDEP risk factors
- Uncontrolled generalized tonic-clonic seizures, nocturnal seizures, poor medication adherence, and young adult male sex increase sudden unexpected death in epilepsy risk; supervision and adherence counseling help.
- Albuminocytologic dissociation
- Elevated CSF protein with normal cell count, typical of Guillain-Barre syndrome after the first week; it supports the diagnosis alongside progressive areflexic weakness.
- Repetitive nerve stimulation decrement
- A greater than 10% decline in compound muscle action potential amplitude with low-frequency stimulation supports myasthenia gravis, reflecting postsynaptic neuromuscular junction failure.
- CMT1A genetics
- Charcot-Marie-Tooth type 1A results from a PMP22 duplication on chromosome 17p11.2, causing uniform demyelinating conduction slowing, distal weakness, and pes cavus.
- Fibrillation potentials
- Spontaneous EMG discharges of denervated muscle fibers appearing weeks after nerve injury; they indicate active denervation and are absent in acute injury.
- McDonald criteria
- Multiple sclerosis diagnosis requires dissemination in space and time; CSF oligoclonal bands can substitute for dissemination in time when typical MRI lesions are present.
- Area postrema syndrome
- Refractory nausea, vomiting, or hiccups from a medullary lesion, a core clinical feature of neuromyelitis optica spectrum disorder associated with anti-aquaporin-4 antibodies.
- Anti-LGI1 encephalitis
- Autoimmune encephalitis with faciobrachial dystonic seizures, hyponatremia, and limbic MRI changes; it responds to corticosteroids and immunotherapy, often without a tumor.
- Longitudinally extensive myelitis
- A spinal cord lesion spanning three or more vertebral segments, characteristic of neuromyelitis optica spectrum disorder and also seen in MOG antibody disease.
- Progressive supranuclear palsy
- Atypical parkinsonism with vertical supranuclear gaze palsy, early falls, axial rigidity, and frontal cognitive impairment; levodopa response is poor and no disease-modifying therapy exists.
- Huntington disease genetics
- Autosomal dominant CAG trinucleotide repeat expansion in the HTT gene; 36 or more repeats is pathogenic, and larger repeats cause earlier onset with anticipation.
- Tardive dyskinesia treatment
- Involuntary orofacial movements after chronic dopamine antagonist exposure; VMAT2 inhibitors such as valbenazine or deutetrabenazine are first-line, while anticholinergics may worsen symptoms.
- Cluster headache treatment
- High-flow oxygen and subcutaneous sumatriptan abort attacks; verapamil is first-line prophylaxis, with a baseline ECG because of dose-dependent bradycardia and heart block.
- Trigeminal neuralgia
- Paroxysmal electric-shock facial pain in the V2 or V3 distribution triggered by touch or chewing; carbamazepine or oxcarbazepine is first-line, and MRI excludes vascular compression.
- Medication-overuse headache
- Headache on 15 or more days monthly with overuse of acute medications for more than three months; treatment requires withdrawal of the overused drug and prophylactic therapy.
- MGMT promoter methylation
- Methylation silences the DNA repair gene MGMT and predicts benefit from temozolomide in glioblastoma, guiding standard chemoradiation decisions.
- Primary CNS lymphoma biopsy
- Stereotactic biopsy is required before corticosteroids because steroids can rapidly lyse tumor cells and obscure histology; high-dose methotrexate is first-line therapy.
- Dexamethasone for tumor edema
- Corticosteroids reduce peritumoral vasogenic edema and intracranial pressure from brain tumors; they do not treat the tumor itself and are tapered after definitive therapy.
- Listeria meningitis coverage
- Ampicillin is added to empiric vancomycin plus ceftriaxone for adults over 50 or immunocompromised patients because Listeria is resistant to cephalosporins.
- HSV encephalitis
- Fever, altered consciousness, seizures, and temporal lobe MRI changes; start intravenous acyclovir immediately and confirm with CSF PCR, since early treatment improves outcome.
- PML imaging
- JC virus demyelination shows asymmetric, non-enhancing white matter lesions without mass effect; treatment is restoring immune function, and immune reconstitution inflammatory syndrome may follow.
- Lewy body dementia
- Dementia with fluctuating cognition, visual hallucinations, parkinsonism, and REM sleep behavior disorder; patients are highly sensitive to antipsychotics, and cholinesterase inhibitors may help.
- Normal pressure hydrocephalus
- Gait disturbance, urinary incontinence, and cognitive decline with ventriculomegaly; a large-volume lumbar puncture or lumbar drain trial predicts response to shunt placement.
- Internuclear ophthalmoplegia
- Impaired adduction with contralateral abducting nystagmus from a medial longitudinal fasciculus lesion; bilateral in multiple sclerosis, unilateral in brainstem infarction.
- Pupil-involving third nerve palsy
- Ptosis with a down-and-out pupil-dilated eye suggests a compressive lesion such as a posterior communicating artery aneurysm and requires urgent CT angiography.
- Cauda equina syndrome
- Saddle anesthesia, urinary retention, bilateral leg weakness, and areflexia require urgent MRI and surgical decompression within 24-48 hours to prevent permanent deficit.
- Autonomic dysreflexia
- In spinal cord injury above T6, noxious stimuli cause severe hypertension, bradycardia, and headache; treat by removing the trigger and using antihypertensives if needed.
- Monro-Kellie doctrine
- The rigid skull contains brain, blood, and CSF; an increase in one compartment must be offset by a decrease in another, or intracranial pressure rises.
- Ischemic penumbra thresholds
- Cerebral blood flow below about 20 mL/100 g/min causes electrical failure, while below about 10 mL/100 g/min causes membrane failure and infarction; the penumbra is salvageable tissue.