Neurology I Flashcards

1
Q

A “steppage gait” secondary to foot drop is often caused by […] radiculopathy and common peroneal neuropathy.

A

A “steppage gait” secondary to foot drop is often caused by L5 radiculopathy and common peroneal neuropathy.

both pathologies result in weakness with dorsiflexion; L5 radiculopathy also causes weak foot inversion and plantar flexion, as well as back pain radiating to the foot

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2
Q

A “steppage gait” secondary to foot drop is often caused by L5 radiculopathy and […] neuropathy.

A

A “steppage gait” secondary to foot drop is often caused by L5 radiculopathy and common peroneal neuropathy.

both pathologies result in weakness with dorsiflexion; L5 radiculopathy also causes weak foot inversion and plantar flexion, as well as back pain radiating to the foot

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3
Q

A pure motor stroke is typically caused by a lacunar infarct of the […] limb of the internal capsule.

A

A pure motor stroke is typically caused by a lacunar infarct of the posterior limb of the internal capsule.

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4
Q

Abortive treatment for cluster headaches includes […] (preferred) or sumatriptan.

A

Abortive treatment for cluster headaches includes 100% O2 (preferred) or sumatriptan.

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5
Q

Acute angle-closure glaucoma is characterized by sudden vision loss with “[…]” around lights.

A

Acute angle-closure glaucoma is characterized by sudden vision loss with “halos” around lights.

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6
Q

Acute subdural hematomas appear […]-dense on CT.

A

Acute subdural hematomas appear hyper-dense on CT.

red arrows; versus chronic SDH, which is typically hypodense on CT (blue arrows)

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7
Q

Acute-onset focal neurological findings, fever, and behavioral changes in a young patient are suggestive of […] encephalitis.

A

Acute-onset focal neurological findings, fever, and behavioral changes in a young patient are suggestive of HSV encephalitis.

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8
Q

Alcoholic cerebellar degeneration is caused by damage to the […] cells in the anterior cerebellar vermis.

A

Alcoholic cerebellar degeneration is caused by damage to the Purkinje cells in the anterior cerebellar vermis.

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9
Q

Alcoholic […] degeneration typically affects patients with extensive alcohol abuse and presents with progressive wide-based gait and postural instability.

A

Alcoholic cerebellar degeneration typically affects patients with extensive alcohol abuse and presents with progressive wide-based gait and postural instability.

other signs of cerebellar damage include intention tremor, hypotonia, and dysdiadochokinesia; truncal coordination is impaired (e.g. tandem gait) but limb coordination is typically intact (e.g. finger-nose testing)

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10
Q

Are patients with pseudodementia typically distressed by their memory impairment?

A

Yes

helpful distinguishing feature from Alzheimer’s dementia, in which patients are relatively unconcerned

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11
Q

Are steroids useful in the management of Guillain-Barre syndrome?

A

No

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12
Q

Brain abscess is often visualized on CT or MRI as a […] lesion with central necrosis.

A

Brain absess is often visualized on CT or MRI as a ring-enhancing lesion with central necrosis.

a single absess typically results from direct extension of adjacent infection

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13
Q

Broca (expressive) aphasia is characterized by […] repetition (intact or impaired).

A

Broca (expressive) aphasia is characterized by impaired repetition (intact or impaired).

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14
Q

Broca (expressive) aphasia is characterized by […] comprehension (intact or impaired).

A

Broca (expressive) aphasia is characterized by intact comprehension (intact or impaired).

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15
Q

Broca (expressive) aphasia is characterized by […] speech (fluent or nonfluent).

A

Broca (expressive) aphasia is characterized by nonfluent speech (fluent or nonfluent).

i.e. agrammatic speech

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16
Q

Brown-Sequard syndrome presents with […]-lateral loss of pain and temperature below the level of the lesion (due to spinothalamic tract damage).

A

Brown-Sequard syndrome presents with contra-lateral loss of pain and temperature below the level of the lesion (due to spinothalamic tract damage).

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17
Q

Brown-Sequard syndrome presents with […]-lateral loss of vibration, proprioception, and touch below the level of the lesion (due to dorsal column damage).

A

Brown-Sequard syndrome presents with ipsi-lateral loss of vibration, proprioception, and touch below the level of the lesion (due to dorsal column damage).

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18
Q

Brown-Sequard syndrome presents with […]-lateral upper motoneuron signs below the level of the lesion (due to corticospinal tract damage).

A

Brown-Sequard syndrome presents with ipsi-lateral upper motoneuron signs below the level of the lesion (due to corticospinal tract damage).

e.g. weakness, spastic paralysis, positive babinski

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19
Q

Can a patient be diagnosed with brain death if they have intact deep tendon reflexes?

A

Yes

brain death is characterized by absent cortical and brain stem function; the spinal cord may still be functioning

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20
Q

Can a patient with severe, acute pain refractory to NSAIDs and a history of IV drug abuse be given opioids for acute pain management?

A

Yes

management of acute pain is similar for all patients, regardless of substance abuse history

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21
Q

Can epidural hematomas cross suture lines?

A

No

important distinguishing feature from subdural hematoma

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22
Q

Can subdural hematomas cross suture lines?

A

Yes

important distinguishing feature from epidural hematoma

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23
Q

Cancer of what organ most commonly metastasizes to the brain?

A

Lung

lung > breast > melanoma > GI

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24
Q

Carotid endarterectomy should be considered for symptomatic patients (e.g. TIA, stroke) with carotid stenosis between […] - […]% to reduce future stroke risk.

A

Carotid endarterectomy should be considered for symptomatic patients (e.g. TIA, stroke) with carotid stenosis between 70 - 99% to reduce future stroke risk.

patients with disabling neurologic deficits, 100% occlusion of the carotid artery, or life expectancy < 5 years are unlikely to benefit

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25
Q

Cauda equina syndrome may be associated with “[…] anesthesia”.

A

Cauda equina syndrome may be associated with “saddle (S3-S5) anesthesia”.

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26
Q

Cauda equina syndrome occurs due to compression of […] from L2 and below.

A

Cauda equina syndrome occurs due to compression of spinal nerve roots from L2 and below.

thus a lesion of the peripheral nervous system; usually caused by intravertebral disk herniation or tumors

27
Q

Central retinal artery occlusion is characterized by acute, […] monocular vision loss (painful or painless).

A

Central retinal artery occlusion is characterized by acute, painless monocular vision loss (painful or painless).

28
Q

Central retinal artery occlusion is most commonly caused by an embolized atherosclerotic plaque from the ipsilateral […] artery.

A

Central retinal artery occlusion is most commonly caused by an embolized atherosclerotic plaque from the ipsilateral internal carotid artery.

29
Q

Cerebral amyloid angiopathy is associated with […] dementia.

A

Cerebral amyloid angiopathy is associated with Alzheimer’s dementia.

it is not associated with systemic amyloidoses

30
Q

Cerebral sinus thrombosis typically occurs in patients with […] conditions and manifests as headache and signs of intracranial hypertension (e.g. nausea/vomiting, papilledema).

A

Cerebral sinus thrombosis typically occurs in patients with hypercoaguable conditions and manifests as headache and signs of intracranial hypertension (e.g. nausea/vomiting, papilledema)
hypercoaguable conditions include contraceptive use, pregnancy, malignancy, and inherited disorders.

31
Q

Chronic subdural hematomas appear […]-dense on CT and typically manifest as headache, somnolence, confusion, and focal neurologic deficits.

A

Chronic subdural hematomas appear hypo-dense on CT and typically manifest as headache, somnolence, confusion, and focal neurologic deficits.

e.g. mild trauma, cerebral atrophy, elderly, alcoholism (blue arrow)

32
Q

Cleavage of SNARE proteins via tetanus toxins inhibits the release of […] and glycine from Renshaw cells in the spinal cord.

A

Cleavage of SNARE proteins via tetanus toxins inhibits the release of GABA and glycine from Renshaw cells in the spinal cord.

GABA and glycine are inhibitory neurotransmitters, therefore, there is a lack of motor inhibition

33
Q

Cleavage of SNARE proteins via tetanus toxins inhibits the release of GABA and […] from Renshaw cells in the spinal cord.

A

Cleavage of SNARE proteins via tetanus toxins inhibits the release of GABA and glycine from Renshaw cells in the spinal cord.

GABA and glycine are inhibitory neurotransmitters, therefore, there is a lack of motor inhibition

34
Q

Common early side effects of levodopa/carbidopa include dizziness, headache, agitation, and visual […].

A

Common early side effects of levodopa/carbidopa include dizziness, headache, agitation, and visual hallucinations.

involuntary movements (e.g. dyskinesia) typically occur after 5 - 10 years of therapy

35
Q

Common presenting symptoms of cavernous sinus thrombosis include severe […], periorbital edema, and ophthalmoplegia.

A

Common presenting symptoms of cavernous sinus thrombosis include severe headache, periorbital edema, and ophthalmoplegia.

36
Q

Conduction aphasia is caused by damage to the […], which is a large fiber bundle that connects Broca’s area with Wernicke’s area.

A

Conduction aphasia is caused by damage to the arcuate fasciculus, which is a large fiber bundle that connects Broca’s area with Wernicke’s area.

37
Q

Conduction aphasia is characterized by […] speech (fluent or nonfluent).

A

Conduction aphasia is characterized by fluent speech (fluent or nonfluent).

38
Q

Conduction aphasia is characterized by […] repetition (intact or impaired).

A

Conduction aphasia is characterized by impaired repetition (intact or impaired).

39
Q

Conduction aphasia is characterized by […] comprehension (intact or impaired).

A

Conduction aphasia is characterized by intact comprehension (intact or impaired).

40
Q

Conservative treatment of pseudotumor cerebri includes […].

A

Conservative treatment of pseudotumor cerebri includes weight loss.

41
Q

Craniopharyngioma is a CNS tumor that arises from epithelial remnants of […].

A

Craniopharyngioma is a CNS tumor that arises from epithelial remnants of Rathke’s pouch (oral ectoderm).

42
Q

Craniopharyngioma typically presents as a supratentorial mass in a […] or […] (age group).

A

Craniopharyngioma typically presents as a supratentorial mass in a child or young adult (age group).

while most common in children, nearly 50% of craniopharyngiomas occur in

43
Q

Creutzfeldt-Jakob disease is characterized by periodic […] complexes on EEG.

A

Creutzfeldt-Jakob disease is characterized by periodic sharp wave complexes on EEG.

clasically sharp, triphasic, synchronous discharges are seen on EEG

44
Q

CSF analysis in patients with idiopathic intracranial hypertension typically reveals an opening pressure > […] mm H2O with an otherwise normal analysis.

A

CSF analysis in patients with idiopathic intracranial hypertension typically reveals an opening pressure > 250 mm H2O with an otherwise normal analysis.

45
Q

Diabetic neuropathy strictly affects […] motor neurons (upper or lower).

A

Diabetic neuropathy strictly affects lower motor neurons (upper or lower).

thus, signs of UMN lesion (e.g. hyperreflexia, positive Babinski sign) are suggestive of another disease process

46
Q

Do patients with cerebellar lesions sway with their eyes open or closed?

A

Both

important distinguishing feature from dorsal column lesions (sway with eyes closed only; Romberg sign)

47
Q

Do patients with dorsal column lesions sway with their eyes open or closed?

A

Closed (Romberg sign)

important distinguishing feature from cerebellar lesions (sway with eyes open and closed)

48
Q

Do the symptoms of Lambert-Eaton syndrome improve with administration of an AChE inhibitor (e.g. edrophonium)?

A

No

treatment may include guanidine and/or 3,4-diaminopyridine to increase presynaptic acetylcholine levels

49
Q

Do the symptoms of myasthenia gravis improve with administration of an AChE inhibitor (e.g. edrophonium)?

A

Yes

50
Q

Does amyotrophic lateral sclerosis (ALS) damage upper or lower motoneurons?

A

Both

damages ventral horn (LMNs) and corticospinal tract (UMNs)

51
Q

Does cauda equina syndrome present with upper or lower motor neuron symptoms?

A

Lower only

helpful distinguishing feature from conus medullaris syndrome, with causes both upper and lower motor neuron symptoms

52
Q

Does cleavage of SNARE via botulinum toxin prevent release of excitatory or inhibitory neurotransmitters?

A

Excitatory (thus causing flaccid paralysis)

53
Q

Does cleavage of SNARE via tetanus toxin prevent release of excitatory or inhibitory neurotransmitters?

A

Inhibitory (thus causing spastic paralysis)

54
Q

Does conus medullaris syndrome present with upper or lower motor neuron symptoms?

A

Both upper and lower

helpful distinguishing feature from cauda equina syndrome, which causes lower motor neuron symptoms only

55
Q

Does multiple sclerosis cause hemiparesis or hemisensory symptoms?

A

Can cause either or both

56
Q

Early-onset dementia with Parkinsonian features is suggestive of […] dementia.

A

Early-onset dementia with Parkinsonian features is suggestive of Lewy body dementia.

however, if Parkinsonism predates cognitive impairment by > 1 year, the diagnosis is Parkinson disease dementia

57
Q

Epidural hematoma is due to rupture of the […] artery (branch of maxillary artery).

A

Epidural hematoma is due to rupture of the middle meningeal artery (branch of maxillary artery).

58
Q

Essential tremor is […] with movement or when anxious (relieved or worsened).

A

Essential tremor is worsened with movement or when anxious (relieved or worsened).

important distinguishing feature from resting tremor (better with movement)

59
Q

Following intubation, myasthenic crisis is managed with […] (preferred) or […], as well as corticosteroids.

A

Following intubation, myasthenic crisis is managed with plasmapheresis (preferred) or IVIG, as well as corticosteroids.

60
Q

Foodborne botulism in adults is associated with ingestion of improperly canned foods and aged […].

A

Foodborne botulism in adults is associated with ingestion of improperly canned foods and aged seafood (e.g. cured fish).

61
Q

Frontotemporal dementia is characterized by […] aggregates (shape) of hyperphosphorylated tau protein known as Pick bodies; may be seen with silver stain.

A

Frontotemporal dementia is characterized by round aggregates (shape) of hyperphosphorylated tau protein known as Pick bodies; may be seen with silver stain.

versus neurofibrillary tangles in Alzheimer’s disease

62
Q

Frontotemporal dementia is characterized by round aggregates (shape) of hyperphosphorylated tau protein known as […]; may be seen with silver stain.

A

Frontotemporal dementia is characterized by round aggregates (shape) of hyperphosphorylated tau protein known as Pick bodies; may be seen with silver stain.

versus neurofibrillary tangles in Alzheimer’s disease

63
Q

Glioblastoma multiforme (GBM) is a malignant, high-grade tumor of […] (cell type).

A

Glioblastoma multiforme (GBM) is a malignant, high-grade tumor of astrocytes (cell type).

also known as grade IV astrocytoma