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329 Cards in this Set

  • Front
  • Back

**


What characterizes the memory loss in patients with dissociative amnesia?

Episodic

Amnesia preceded by epigastric sensation/fear are associated with electrical abnormalities where?

Temporal Lobe

Memory loss pattern in dissociative amnesia.

Occurs for a discrete period of time.

Amnesia characterized by loss of memory of events that occur after onset of etiologic condition/agent

Anterograde

This psychoactive drug produces amnesia.

Alcohol

Patient with strange behavior answers appropriately with fluent speech but no ability to retain new info. Episode lasts 6 hours then back to normal without recollection of events.

Transient Global Amnesia

Patient reports hearing voices of someone not present. Patient stops moving, stares blankly, repetitively picks at clothing, does not respond to questions/commands for several minutes. Resolves after 15 minutes and patient can't recall events.

Complex Partial Seizure

55yo brought in by family after episode of amnesia/bewilderment lasting hours. CVA ruled out. Patient keeps asking what is happening. Which medication?

Observation with no pharmacological intervention

Sense of loss of identity often following a traumatic experience and associated with inability to recall one's past.

Dissociative Fugue

Contralateral leg weakness with sparing of face and arms. Urinary incontinence and abulia. Where is the lesion?

Anterior Cerebral Artery

***** *****


Visual problem in pituitary tumor compressing optic chiasm.

Bitemporal hemianopsia

***** ***


60yo right-handed M gets lost frequently, only writes on right half of paper. Left-sided hemi-neglect. Where is the lesion?

R Parietal

*****


66yo with frequent falls, months of anxiety, unwilling to leave home. Mild impairment of vertical gaze on smooth pursuit/saccades. Mild axial rigidity, mild upper extremity rigidity, mild slowness of movement with normal posture. Dx ?

Progressive Supranuclear Palsy

****


65yo patient fell several times in the past 6 months. MSE wnl, smooth pursuit and saccades impaired and worse with vertical gaze. Full ROM on head, mild symmetric rigidity, no tremor. MRI/CSF/labs unremarkable. Dx?

Progressive Supranuclear Palsy

***


26yo with headache, clumsiness of R hand for weeks. Struggles with rapid alternating movements of R hand, overt intention tremor with finger-to-nose. CNs wnl, no papilledema. Lesion?

Cerebellum

9yoF has a 3 months history of unprovoked laughter. Worse when not sleeping well. Patient is not happy during laughing episodes. Started menstruating 6 months ago. Tanner 4. Dx?

Hypothalamic Hamartoma/Gelastic Seizure

**


5yo with 4 month h/o morning HA, emesis, ataxia, falls, diplopia. Lesion?

Medulloblastoma

75yo evaluated for progressive ataxia, urine incontinence, cognitive decline. After removal of CSF, there is improvement in gait and balance. What would the CT show?

Enlargement of the frontal horns

70yo develops confusion, lethargy, generalized tonic-clonic seizure. Lab reveals serum sodium of 95. Most likely complication of excessively rapid correction?

Central Pontine Myelinolysis

Where is the lesion that causes bilateral coarse nystagmus worsening with visual fixation and is present with horizontal and vertical gaze?

Brainstem

32yo with 1 month h/o worsening HA, episodic mood swings, and occasional hallucinations. Hallucinations are visual, tactile, and auditory. CT head reveals tumor where?

Temporal Lobe

Fluent speech, preserved comprehension, inability to repeat speech. No associated signs. Where is the lesion?

Supramarginal Gyrus or Insula

Acute onset of hemiballismus of LUE & LLE. MRI shows lesion where?

Subthalamic Nucleus

43yo with newly dx AIDS has increasing social withdrawal and irritability over weeks. Can't remember phone number, unable to do chores, seems distracted. R hemiparesis, L limb ataxia, bilateral visual field defects. LP normal. Dx?

Progressive Multifocal Leukoencephalitis

Unconsciousness can be induced by a small area of damage where?

Reticular Formation

Patient admitted to ED after MVA. Receives D5. Later experiences confusion, oculomotor paralysis, and dysarthria. Sx caused by?

Wernicke's Encephalopathy

Patient reports HA and loss of peripheral vision. Visual field defects of both temporal fields of oth eyes. MRI shows?

Mass in Sella Turcica

37yoF w/ discoid lupus controlled on stable dose of PO prednisone. Abrupt development of fatigue, inflamed joints, diffuse myalgia. Depressed mood + cognitive impairment. No prior psych history or focal neuro signs. Dx?

Disease-Induced Cerebritis

25yo with diplopia and difficulty balancing. R lateral gaze shows weakness of L medial rectus w/ nystagmus of R eye. L lateral gaze shows weakness of R medial rectus w/ nystagmus of L eye. Mild finger-nose ataxia on R. Dx?

Multiple Sclerosis

52yo with gait difficulty. Mild dysarthria, mild finger-nose ataxia, minimal heel-shin ataxia. Romberg negative but unsteady while walking. Broad-based lurching gait. Plantar reflexes are flexor. Imaging demonstrates?

Cerebellar vermis atropy

Syndrome associated with occlusion of the cortical branch of the posterior cerebral artery.

Homonymous Hemianopia with alexia without agraphia.

34yoM for psych eval 5y after TBI @ work. Since accident, overly talkative/restless. Divorced because he was acting irresponsible and lost job. Psychometrics show avg intelligence, no memory deficits. Lesion is where?

Frontal Lobe

Child starts kindergarten, is more emotionally reactive and regresses at home. Teacher says child is normal at school. What accounts for the change noticed by parents?

Normative response to stress 2/2 school transition

Which cancer has the highest chance of going to the brain?

Lung

Which hormone is secreted in a functional pituitary adenoma?

Prolactin

CT + MRI shows ventriculomegaly out of proportion to sulcal atrophy. Dx?

Normal Pressure Hydrocephalus

20yo with 1y h/o bitemporal HA, polydipsia, polyuria, and bulimia with 2mo h/o emotional outbursts, aggression, and transient confusion. Neuro exam normal. MRI shows?

Hypothalamic Tumor

Previously pleasant mom becomes profane and irresponsible over 6 months. Lesion is where?

Frontal Lobe

Unilateral hearing loss, vertigo, unsteadiness/falls, HA, mild facial weakness, ipsilateral limb ataxia. Lesion is where?

Cerebellopontine Angle

38yoF with muscle spasm of proximal limbs and trunk, lumbar lordosis while walking. EMG abnormal. Serum antiglutamic acid antibodies.

Stiff-Person Syndrome

Pituitary tumor that protrudes though the diaphragmatic sella is most likely to cause?

Bitemporal hemianopsia

Conduction aphasia often 2/2 damage to what?

Arcuate Fasciculus

70yo develops flaccid paralysis following severe H2O intoxication. Dysphagia + dysarthria w/o other cranial nerve involvement. Sensory exam limited but grossly normal. DTR symmetric. Cognition intact. Dx?

Central Pontine Myelinolysis

MRI finding for woman with memory decline, urinary incontinence, and trouble walking

Dilation of Ventricles

Patient draws clock with hemiagnosia. Lesion?

Parietal Lobe

Effortful nonfluent speech with decreased speech output. Lesion?

Anterior Frontal Gyrus

**


Which term describes a state of immobility that is constantly maintained?

Catalepsy

52yo with h/o unipolar depression brought to ED with first episode catatonia. No meds, UDS negative. Workup should focus on what?

Metabolic disorders

Among inpatients, catatonia occurs most frequently in the context of what illness?

MDD

21yo recently diagnosed with schizophrenia becomes mute, occasionally parrots words. What subtype of schizophrenia is this?

Catatonic

Symptoms that dominate mood disorder with catatonia.

Purposeless motor activity not influenced by external stimuli.

***** ***


62yoM with DM is not making sense saying "thar szing is phrumper zu stalking." Normal intonation but no one in the family can understand it. He verbally responds to questions with similar phrases but fails to execute any instruction. Dx?

Wernicke's Aphasia

***** ***


66yo with HTN develops vertigo, diplopia, n/v, hiccups, L face numbness, nystagmus, hoarseness, ataxia of limbs, staggering gait, tendency to fall to the left. Dx?

Lateral Medullary Stroke

**


Patient with chronic Afib develops aphasia and R hemiparesis at noon. ER exam notes weakness of R extremities and severe dysfluent aphasia, but CT at 1330 has no acute lesion. Most appropriate TX?

TPA

**


Rapid onset of R facial weakness, left limb weakness, diplopia. Dx?

Brain Stem Infarct

**


A life threatening complication of cerebellar hemorrhage.

Acute hydrocephalus

**


72yo with embolic infarct in MCA. Cardiac US shows no structural abnormalities. Carotid Doppler shows <50% occlusion of either side. EKG reveals AFib. Which strategy has the best likelihood of reducing strokes in this patient?

Warfarin

**


Young adult gained 70lbs in last year and complains of daily severe HA sometimes associated with grayed out vision. Papilledema present. CT + MRI show ventricles smaller than usual. Goal of tx?

Prevent blindness

**


68yo with HTN develops rapidly progressing RUE + RLE weakness w/ deviation of eyes to left. W/in 30 min of onset, pt becomes sleepy. 2h after onset patient is unresponsive. Dense R hemiplegia, eyes deviated to left. PERRL. R facial weakness to grimace. Cough and gag present. CT finds?

L Putaminal Hemorrhage

**


Superior homonymous quadrantic defects in visual fields result from lesions to which structure?

Temporal Optic Radiations

**


78yo h/o ischemic stroke w/ residual mild hemiplegia. Unaware that there's a problem of weakness. When asked to raise the weak arm, patient raises normal arm. Neglects weak side of the body. Where is the lesion?

Parietal Lobe

**


Patient has multiple stroke-like sx of short duration over several days. New-onset sx for last 90 min. CT is negative for hemorrhage. Appropriate tx?

IV Thrombolytics

**
MRI scan of head reveals an infarct in distribution of L ACA. Patient most likely exhibits?

Contralateral LE weakness

Pure sensory deficit extending to midline and involving face, arm, trunk, and leg. Where is the lacunar infarct?

Lateral Thalamus

Head CT w/ lens-shaped hyperdensity

Epidural Hematoma

50yo patient has VH of children playing. VH are fully formed, colorful, vivid, without sound. Patient is amused rather than scared. Normal language, memory, cranial nerves. No weakness or involuntary movement. No sensory deficit. DTR symmetric. CSF/UDS wnl. Dx?

PCA ischemia

R palsy with equal involvement of face, arm, leg combined with CN3 palsy. Most likely an occlusion of a branch of what?

PCA

Hemisensory loss followed by pain and hyperpathia involving all modalities. Reaches midline of trunk and head. Which artery is ischemic?

PCA

Most common manifestation of acute neurosyphillis

Stroke

65yo wakes with R hemiparesis and motor aphasia. Eval completed w/in 1h. Neuro exam has no other abnormalities. Head CT w/o contrast negative. Next step?

ASA

65yo falls 2/2 stroke. Weak RLE, minor weakness in RUE. No face weakness, no sensory deficit. Speech unaffected. Unusually quiet and passive. Where is the stroke?

L ACA

58yoM with w/o HTN, smoking, sudden inability to speak. Face droop and leg drag on R side. Seen in ER w/in 40 min of onset. Aphasic, cannot understand or repeat. Unintelligible sounds for speech. Alert but frustrated. Arm and face weaker than leg. CT Head neg for hemorrhage. Pathology and location?

Thromboembolic Stroke of L MCA

Abulia is an impairment in?

Spontaneous movement and speech.

Sudden onset vertigo, nausea, hoarseness/dysphagia, R sided face numbness, diminished R gag, decreased pinprick and temperature sensation on L. Lesion?

R Medullary Infarct

65yo DM patient presents w/ acute L sided weakness, deviation of gaze to R, L hemipelgia and hemisensory deficit, L homonymous hemianopsia. 12h later, patient is unconscious, L pupil enlarged and unreactive. CT shows?

R MCA infarct, Edema, Uncal Herniation

Patient with acute onset vertigo, what will suggest R lateral medullary infarct?

R facial loss of touch and temperature sensation

46yoM with diplopia and R eye pain. Ptosis of R eyelid, inability to elevate or adduct R eye + R pupillary dilation. Cause?

Posterior Communicating Artery Aneurysm

Aphasia with effortful, fragmented, non-fluent, telegraphic speech. Lesion is where?

Posterior Frontal Lobe

39yo patient with h/o multiple miscarriages develops an acute L sideded hemiparesis. Work-up reveals elevated anticardiolipin titers and no other risk factors for stroke.
Next step?

Plasmapheresis

Abnormal elevated metabolic findings associated with increased risk of stroke in patients under 50.

Plasma Homocysteine

70yo patient hospitalized because of MCA stroke. Psych eval shows non-fluent aphasia. What most likely characterized the patient's interaction with the psychiatrist?

The patient was able to follow the verbal request "close your eyes".

Acute onset dense sensorimotor deficit in contralateral face/arm, mild involvement of LE. Associated with gaze deviation towards opposite side of deficit. Occlusion?

Superior Division of MCA

Weakness of extension at knee involves a lesion of which nerve?

Femoral

CT scan w/ occipital and intraventricular hyperintensities.

Parenchymal Hemorrhage

Which med has secondary prevention against embolic stroke in patients with Afib?

Warfarin

As opposed to strokes caused by arterial embolism or thrombosis, those cause by cerebral vein or venous sinus thrombosis are?

Associated with seizures at onset

Atrophy of R temporal lobe on cross section associated with occlusion of?

MCA

Loss of ability to execute previously learned motor activities (not due to weakness/ataxia/sensory loss) is associated with lesions of what?

L Parietal Cortex

58yo s/p CABG has anomia for fingers and body parts, errors involving left/right, inability to write thoughts/take notes/make calculations. Fluent speech and excellent comprehension. Etiology?

L Medial Temporal Stroke

Visual disturbances associated with occlusion of R PCA?

L Homonymous Hemianopsia

65yo with HTN collapsed. Stuporous, R hemiparesis + hemisensory deficit. Eyes deviate to L. CT would show intraparenchymal hemorrhage in what?

L Basal Ganglia

Lower facial weakness with relative sparing of forehead. Stroke occurred where?

Internal Capsule

Which location for stroke has a high frequency and greater severity of depression?

L Anterior Frontal

68yo patient is depressed following hip surgery. Withdrawn, looks blank, shows dysarthria, weakness, PMR, hyperreflexia, trouble swallowing. MRI shows?

Periventricular White Matter Demyelination

Prognosis of acute inflammatory demyelinating polyneuropathy is poorest if the disease process involves which of the following?

Proximal Axon

Patient with HTN. Painless blindness in L eye with afferent pupillary defect. MRI shows several T2 hyperintensities in white matter periventricularly. No corpus callosum lesions. No enhancement with gadolinium. Diagnosis?

Ischemic Optic Neuropathy

63yo with new-onset aphasia and R hemiparesis. 2 day ago had milder/similar sx that resolved in 30 minutes. Yesterday had one for 45 minutes. Current sx started 1.5h ago CT neg for stroke and hemorrhage. TX?

IV Thrombolytics

Prosopagnosis is?

The inability to recognize faces

57 year old diabetic w/ HTN has episodes of vision loss like a "curtain falling" over L eye. Transient speech + language disturbance, mild R hemiparesis that lasts 2 hours. Presence of what?

Extracranial L Internal Carotid Stenosis

Head Injury w/ LOC. Hours long lucid interval leads to rapidly progressing coma. Hemorrhage?

Epidural

Pt in ED with sudden HA and collapsing, some lethargy. Rigid neck, no papilledema, no focal CN/motor signs. Initial test?

CT head

Post-stroke depression in 80yo R handed patient is associated with cognitive impairments that:

Correlate with L hemispheric involvement

Fluent speech with preserved comprehension and inability to repeat statements

Conduction aphasia

Normal romberg w/ eyes open but loses balance with eyes closed. Location?

Cerebellar Vermis

65yo w/ HTN, Meniere's. N/V worse w/ head movement. R beating nystagmus on lateral gaze, finger-nose is ataxic, poor balance, dysarthria. Dx?

Cerebellar infarct

66yoM w/ sudden occipital HA, vertigo, slurred speech. Eyes: small reactive pupil, R gaze, nystagmus, blobbing. CN: R facial weakness, poor R corneal reflex Motor: truncal ataxia, b/l hyperreflexia + Babinski. Dx?

Cerebellar hemorrhage

Motor speech paradigm activation task on fMRI. Hyperactivity in R temporal. Damage is where?

Calcarine Fissure

Inability to recognize object by touch.

Astereognosis

In managing acute ischemic stroke, administer this w/in 48h of onset to reduce risk of recurrent stroke, disability, death.

ASA

70yo w/ attacks of "whirling sensation", w/n/v, diplopia, dysarthria, tingling of lips. 1 minute, multiple times a day. Patient collapses, is immobilized. No residual s/s, tinnitus, hearing loss, ALOC, or association w/ specific activity. Dx?

Vertebrobasilar insufficiency

Component of type A behavior most reliable as a risk factor for CAD

Hostility

Vascular lesion most characteristic of sudden severe HA, emesis, collapse, preservation of consciousness, few lateralizing signs, neck stiffness.

Subarachnoid Hemorrhage

Patient with sudden onset of L hemiparesis, L homonymous hemianopsia, R gaze, L side neglect. Occlusion of what?

R MCA

70yoF sudden paralysis RLE. RUE slightly affected. No aphasia or visual field deficit. Slower onset of bladder incontinence, abulia, lack of spontaneity. Which vascular area?

L ACA

***** ***


72yo w/ recent behavior/memory problems. Disrobing, not sleeping, irritable. Waxing/waning consciousness. Dx?

Delirium

*****


79yo with decreasing mental state over 3 weeks has an exaggerated startle w/ violent myoclonus. Myoclonic jerks occur spontaneously, ataxia. EEG shows sharp waves. Dx?

Subacute Spongiform Encephalopathy

****


52yo with h/o depression, HTN. Severe HA, "has not been himself" for 10d. Poor eye contact, inattentive, muttering, picking at clothes, occasionally dozes off even at mid-day. Dx?

Delirium

**


Mild confusion, lethargy, thirst, polydipsia

Hyponatremia

**


Multifocal myoclonus in a comatose patient indicates?

Metabolic encephalopathy

**


70yo with mild Alzheimer's lives with family, prescribed an SSRI for MDD. H/O HTN, DM, RA. Acute confusion w/o other med/psych sx. What do you order first?

Electrolytes

What test is most helpful to distinguish dementia vs delirium?

EEG

Alcoholic patient w/ 2 days of confusion, AVH, disorientation, distractibility, fever, tachycardia, tremor. EEG is low voltage fast waves on slow waves. On olanzapine for schizoaffective d/o. Dx?

Delirium, EtOH Withdrawal

Most common EEG finding in metabolic encephalopathy?

Generalized slowing

2d after bowel surgery, 53yo is delirious. Draws a square when asked, but continues to draw a square when asked to draw other things. MSE reveals?

Perseveration

Patient with ICU psychosis most likely has what condition?

Delirium

Best recommendation for patient with delirium?

Maximize Staff Continuity assigned to patient

Delirium in HIV patients is treated with what parenteral agent?

Low dose high-potency antipsychotic

34yo tx for malaria with h/o schizoaffective d/o controlled with risperdal and lithium. Given a single dose of mefloquine. 1 week later, reports anxiety. Escalates to PMA and persecutory delusions. Most likely cause of psychotic sx?

Uncommon SE of new medication

Cancer patient on chemo is disoriented and agitated. Afebrile and VSS. Neuro exam neg. Poor attention, some cognitive impairment. CT ned, EEG shows diffuse slowing.

Haldol

70yo HIV+ IV drug abuser w/ MDD tx with lopinavir, ritonavir, fluoxetine. HepC was dx and treated 2 months ago. Since then patient is irritable, has insomnia and diarrhea. Why?

Drug-Drug interaction

Patient delirious, agitated, hallucinating. Flushed and hot w/ dry skin, mydriasis, tachycardia, diminished bowel sounds. First recommendation?

D/C Anticholinergic Drugs

This major symptom of delirium may require that the patient receive pharmalogical treatment.

Insomnia

***** **


65yoM with 6mo h/o confusion episodes, disorientation, VH of children playing in his room. VH are fully formed, colorful, vivid. Pt has little insight into VH. Normal between episodes. Mild difficulty with serial subtraction, mild symmetric rigidity, bradykinesia. MRI, CSF, labs, UDS neg. Dx?

Lewy Body Dementia

***** **


A limitation of the MMSE

May fail to detect very mild cognitive impairment

***** *


When combined with functional neuroimaging, this biomarker identifies geriatric pt with mild impairment most at risk for Alzheimer's.

E4 APO E allele

**


The most specific factor for distinguishing delirium from dementia of Alzheimer type

Fluctuating Arousal

72yo w/ early dementia. Paranoid + VH. Lightheaded and socially inappropriate. Risperal 0.25mg for 2d leads to confusion, sedation, rigidity. Dx?

Lewy Body Dementia

In addition to orientation, attention, calculation, language, and registration, what other cognitive domain does the MMSE test?

Recall

Tau staining with progressive dementia. Dx?

Alzheimer's Dementia

80yo w/ VH and worsening gate, episodic confusion, disturbed sleep, b/l rigidity, masked facies. Levodopa improved movement temporarily. Dx?

Lewy Body Dementia

Medicine that interferes with the efficacy of Donepezil?

Oxybutinin

A dialysis patient becomes more disoriented and has memory loss. Physical exam normal. Reported that patient has had seizures. Labs and neurodiagnostics negative. Dx?

Dialysis Dementia

Which test correlates most strongly with pre-morbid functioning in early dementia

WAIS-IV Vocabulary Test

71yo with Parkinsonian gait, prominent delusions, fluctuating attention, VH, sensitivity to EPS. Dx?

Lewy Body Dementia

FTD with mutation in Chr17 is associated with abnormal intraneuronal deposition of which protein?

Tau

Neuropsychological test most useful in the early diagnosis of Alzheimer's disease.

10 item world list learning task

Best initial tx of patient with mild Alzheimer's

Cholinesterase Inhibitor

74yo R handed patient with significant memory loss, expressive aphasia. L plantar extensor response. Dx?

Vascular Dementia

Sx most likely related to excessive VitB12

Burning Sensation

60yoF w/ 10 month h/o apathy and depression. Hyperchromic macrocytic anemia. Best test to order next?

VitB12 Level

Earliest evidence of cell loss in patients with Alzheimer's typically occurs in this area of the brain

Entorhinal Cortex

EtOH dependent patient with confusion, ataxia, nystagmus, ophthalmoplegia. High doses of what could prevent this syndrome?

VitB1

Medication helpful in early HIV dementia but is toxic later in the disease

Methylphenidate

74yoF w/ personality change, poor ADLs. Dx?

Pick's Disease

80yo, no prior psych hx. More forgetful, worse ADLs. Can conduct routine social activities. Acquaintances don't notice abnormalities. Dx?

Alzheimer's Dementia

Safest heterocyclic antidepressant for 78yo with depression, agitation, dementia.

Nortriptyline

This cognitive enhancer is an NMDA receptor antagonist

Memantine

Neuronal damage from glutamate excitotoxicity is treated with this.

Memantine

Acamprosate works through this neurotransmitter.

Glutamate

Neurofibrillary tangles in Alzheimer's Dementia are composed of this.

Hyperphosphorylated Tau Proteins

80yo Alzheimer's Dementia patient w/ increasingly combative behavior. Family wants to keep at home. Give which med?

Haldol

Dementia characterized by personality change, attention deficit, impulsivity, affect lability, indifference, perseveration, and loss of executive function. Dysfunction is where?

Frontal Lobe

Binswanger disease has pseudobulbar state, gait disturbance, and this.

Dementia

80yo Alzheimer's pt is brought home for increasingly combative behavior. Daughter would like to keep pt at home if possible. Helpful intervention?

Assessing for caregiver burnout

Early stage HIV type 1 associated dementia has this feature that early onset dementia does not.

Decreased processing speed

Best treatment for agitation in dementia?

Antipsychotics

Clock drawing test is sensitive for this d/o.

Alzheimer's

An amyloid precursor protein is found in this d/o.

Alzheimer's

Most common cause of dementia >65yo.

Alzheimer's
Down's syndrome pt >40yo get this d/o.

Alzheimer's

Characteristic MRI finding in Alzheimer's.

Reduced Hippocampal Volumes

Known risk factors for dementia.


Age


Family Hx


Female


Down's Syndrome


Target of Alzheimer's drugs.
Acetylcholinesterase
Vascular dementia has changes in this structure.

Basal Ganglia
83yo w/ mild HTN, new HA, L hemiparesis. MRI shows R parietal and small occipital hemorrhage. Old R temporal and L parietal hemorrhage. Etiology?

Amyloid Angiopathy
65yo disoriented, mild agitation, VH of children playing. 2 episodes in past, normal between episodes. Mild symmetric rigidity and bradykinesia. MRI, UDS, CSF normal. Etiology?

Lewy Body Dementia

Med most likely to slow progression of vascular dementia.

ASA

Best rationale for cholinesterase inhibitors in Alzheimer's pt.
Reduce neuropsych sx
Pt w/ HIV. Memory loss, inattention, amotivation, poor coordination. Normal LP, atrophy on CT. MRI shows diffuse & confluent white matter changes on T2 w/o enhancement. Dx?

HIV-associated Dementia

Most important tool for eval of early-mod dementia.

MMSE
60yo w/ memory problems (losing things, forgetting names). No other neurocognitive sx. Gradual over years. Former history professor who enjoys intellectual activities. MMSE would be insensitive in this case because of this.

It has a ceiling for the well-educated.

65yo gradual/slow progression of confusion. Anomia, mental slowness, self-neglect, apathy, altered personality, impaired gait, prominent grasp & suck reflexes. Ddx?

Frontotemporal Dementia or Alzheimer's
65yo high school grad w/ MMSE of 23. Score suggests these.

Dementia or Mild Cognitive Impairment
46yo w/o past psych hx over several months becomes labile and irritable. Personality changes w/ inappropriate laughter. In 2 years is convinced all food has germs. Memory intact. Neuropsych testing shows impaired language and attention. Dx?

Frontotemporal Dementia
In regards to memory, dementia rather than depression has this.

Naming Deficits

Bilateral loss of neurons in CA1 (Hippocampus) is the most common histology finding in this.

Alzheimer Dementia

65yo lives alone, increasingly forgetful, difficulty making phone calls and remembering appointments. Lifelong difficulty recalling names. Lives independently. MSE has delayed recall of 4 words. Sx consistent with?

Amnestic mild cognitive impairment
Most common genetic cause of intellectual disability.

Down's Syndrome

Alzheimer's patient in clinic. Daughter is frustrated with caring for her, wants to remover her from her church group. Best initial response?

Tell her to continue going to group.

***** ****


16yo with 1x grand mal. Occasionally has jerks of entire body where they drop things. EEG shows rare 4-6Hz irregular polyspike/wave bursts. Dx?


Juvenile Myoclonic Epilepsy

***** **


8yo w/ staring spells. EEG shows this.


3Hz spike and wave

****


40yo w/ episodes of flailing arm and tonic "fencing" postures. EEG confirms this seizure.


Frontal Lobe


****


10yo with 2-10s lapses of consciousness w/o premonitory sxs. Immediate and full resumption of consciousness. No memory of event. Dx?


Absence Seizure

1st seizure w/ focal onset and secondary generalization in 58yo pt is likely 2/2 this.

Glioblastoma Multiforme
The diagnostic value of transient paresis or aphasia after seizure.

Localization of lesion

6yo w/ brief staring and blinking spells. Best treatment(s).


VPA


Ethosuximide

40yo new onset seizure w/ bilateral thrashing movement. This suggests non-epileptic cause.


Following commands.

Characteristics of normal adult alpha rhythm seen on EEG.

Intermittent and posterior dominant.
Surgical treatment of medication refractory epilepsy.
Vagal stimulation
19yoF has bouts of motor agitation followed by intense meaningless writing. Mood lability, tactile and olfactory hallucinations. Abruptly stops interview to pace the room. Next step is this.

Wait 15min then obtain a prolactin level.
73yoM, routine f/u for seizure d/o. Gum hypertrophy, cerebellar ataxia, hirsutism. The patient is taking this medication.

Phenytoin (Dilantin)

Pt with h/o MDD and well controlled epilepsy seizure free on Wellbutrin 100mg BID. Insurance wants med change to reduce seizure threshold. Has not tried imipramine, nortryptyline, duloxetine, or selegiline. Appropriate response?

Continue Bupropion
Most serious s/e of rTMS.

Seizure
This procedure confirms dx of nonepileptiform seizure.

EEG video telemetry
Tx for juvenile myoclonic epilepsy.

VPA

Complex partial seizures are differentiated from simple partials by this.
Altered Consciousness
Convulsive episode w/ leftward eye deviation, tonic contracture of L side. Post-ictally, eyes deviate to R w/ L side hemiparesis. Focus?

R frontal
28yoF w/ HA. Hyperventilates. Asynchronous tonic-clonic w/o LOC. Dx?

Psychogenic Seizure
In young pt w/ epilepsy, tx depression with this.

Prozac

Why is there a high suicide rate in epileptics?
Comorbid Psychiatric D/O
Lack of prolactin elevation after SZs suggests this etiology.
Psychogenic Seizure
32yo w/ tx refractory complex partials. MRI shows.

Mesial Temporal Sclerosis

Drug-addicted healthcare professional has SZ that isn't withdrawal. Cause?

Meperidine

Complex partial epilepsy aura has this symptom.

Lip Smacking

Head and eyes deviate R and R arm extends immediately before generalized tonic-clonic SZ. Focus?

L cerebral hemisphere

Gustatory special sensory SZ/auras are localized here.

Insular Cortex

This surgery can be used to tx refractory epilepsy.
Stimulation of Vagus Nerve
Pt w/ 1-2 min episodes of altered behavior w/ chewing movements. Pt has no recollection. MRI neg. Dx?

Complex Partial Seizure

28yoF recent onset 1-2 min episodes of altered behavior. Puts clean silverware back in dishwasher, uninterruptible drawing movements. Pt doesn't recall episodes. MRI neg. Dx?
Complex Partial Seizure

16yo w/ new onset tonic clonic. Jerky movements that cause him to drop objects. EEG shows polyspikes. Tx?

Valproic Acid

15yo patient w/ partial complex and secondary generalization, MR, and adenoma sebaceum. Dx?

Tuberous Sclerosis
Adequate initial tx of absence sz in children.

Valproic Acid

***


EEG revealing posterior alpha and anterior beta is obtained in this situation.

Relaxed adult with eyes closed


**


4-6 Hz irregular polyspike in pt with generalized sz is characteristic of this epileptic syndrome.


Juvenile Myoclonic Epilepsy


**


3d s/p cardiac arrest and CPR, 73yoM is comatose. Eyes open, no movement. Doll's eyes elicits full horizontal eye movements. Spontaneous limb movements are symmetrical. Mildly hyperactive reflexes. EEG shows this.


Burst Suppression Pattern


***


28yo with emotional lability and impulsivity. LFT elevated. Close relative has similar sx, died at 30yo from hepatic failure. Diagnostic lab?


Ceruloplasmin

25yo w/ several years of cognitive decline, dysarthria, dysphagia, and slow movement. Hand tremor that increases in amplitude on arm extension. Hepatic disease of unknown etiology. Ocular exam reveals golden brown ring around cornea. Diagnostic lab?

Ceruloplasmin

73yoM w/ onset of fatigue, weight gain, constipation, cold intolerance, depressed mood. R/O this organic cause.

Thyroid

Neuro finding associated with hypothyroidism.
Slow relaxation of DTR
Which patient is indicated for ceruloplasmin titer?

Young adult M w/ new onset emotional lability and movement d/o

Pt with bipolar d/o on lithium for 2y develops rapid cycling. Order this lab.

Thyroid Function

32yo s/p thyroidectomy presents c/o frequent panic attacks, progressive cognitive inefficiency, perceptual disturbances, severe muscle cramps, and carpopedal spasm. Alopecia and absent DTR on exam.

Hypoparathyroidism


***** ***** **


35yoM awakens frequently in the night w/ severe HA, lasts 1-2h, pt is afraid to go to sleep. HA is at L eye, assoc w/ lacrimation, ptosis, miosis. Dx?


Cluster HA
***** **
Young pt w/ new onset severe HA assoc w/ periods of visual obscuration. Neuro exam is normal except for papilledema. MRI neg. Next test?
LP to measure pressure

*****


Abortive tx of common migraines is best achieved w/ this medication.

Rizatriptan


****


Characteristic of post-LP HA.


HA worse w/ sitting upright


***


25yo has HA and emesis. Pain dull, in occiput. Worse when lying down. Severe papilledema b/l. LP shows opening pressure of 80 w/ normal CSF and 120 RBCs in last tube. D-dimer, FDP in blood are elevated. CT normal. Dx?

Sagittal Sinus Thrombosis

**


24yoM w/ nocturnal HA and early waking. Rhinorrhea, nostril blocking, ipsi eye tearing, facial swelling. HA persists 45-60 min. Dx?


Cluster HA


**


35yo w/ episodes of flashing lights traveling L->R in L visual field lasting 30 min followed by difficulty speaking and concentrating. Sx subside but pounding HA and nausea starts. PE and MRI neg. Dx?


Migraine w/ Aura

**


30yo w/ intermittent HAs lasting 1h. Attacks w/ sharp, stabbing pain around eye, tearing, congestion. Most effective abortive?


Oxygen


**


Most effective treatment for acute acute migraine.


Sumatriptan

25yo w/ VH in both visual fields similar to wavy distortions produced by head rising from asphalt. Vertigo, dysarthria, b/l tingling in limbs and mouth followed by occipital HA. Dx?

Basilar Migraine
MOA of Topiramate includes these.


Inhibiting voltage-gated Na channels;


Antagonizing Kainate + AMPA receptors;


Potentiation of GABA-A receptor


28yoF reports severe HAs with n/v. HAs can be incapacitating, preceded by flashes of light in R visual field. During HA can have difficulty expressing herself. Most effective prevention is this.

Topiramate
26yoF with 3d h/o severe continuous non-throbbing HA not improved on NSAID. Mild b/l papilledema. Head CT w/wo contrast shows this.

Sagittal Sinus Thrombosis
Pt c/o severe dull and constant HA not assoc with N/V. Vision loss in L eye, pain and stiffness of limbs. MRI shows periventricular white matter hyperintensities of T2. Elevated sed rate. Next step is this.

High Dose Prednisone
35yo pt w/ 5 min paroxysms of sharp pain around eyes and side of head. 10 times/day. HA with rhinorrhea and conjunctival erythema. This med is most likely to give relief.

Propranolol

***** *


42yoM w/ progressive cognitive deficit develops jerking movements. Imaging shows b/l atrophy of caudate. Pt father had similar illness starting at 50yo. This test confirms dx.

DNA analysis for CAG repeats

*****


This MRI finding most specifically indicates Huntington's.


Caudate Head Atrophy

***


Tx of Huntington's Chorea.


Haloperidol

***


98yoM in ER, unconscious after choking. Progressive neuro d/o presented in early 30s w/ involuntary irregular movements. Evolved into rigid akinesis. Progressive dementia and full time care. Pathology showed generalized atrophy. Dx?


Huntington's Disease

**


35yo pt w/ 2y h/o cognitive decline, difficulty at work, irritability. Restless w/ slow writhing movements in most muscle groups and frequent blinking. Pt's father and paternal grandpa had similar sx and died in their 50s. Dx?


Huntington's Disease

**


Pt w/ depression, 3y h/o change in personality, irritability, impulsive outbursts, and eccentric social interactions. Withdrawn and fidgety. Increased blinking, marked tongue impersistence, mild bradykinesia. Father died of severe dementia at 55yo. Dx?

Huntington's Disease
Disease with trinucleotide repeat expansion

Huntington's Disease
Huntington's Disease etiogene is classified as a polymorphism due to this quality.

Region has many alleles differing in the number of CAG repeats.


****


Role of the hippocampus and parahippocampal gyrus.


Declarative Memory (Facts)

**


Example of declarative memory.


Retention and recall of facts.
Unconscious filling in of memory gap

Confabulation

45yo w/ nystagmus, ataxia, and short term memory loss. Believes wife is possessed by demons. Tx?

Thiamine

A conscious memory that covers for another memory that is too painful to hold in consciousness.

Screen memory

In pt with pronounced deficits in recent memory, remote memory is often...

Deficient on close examination even when it seems well preserved.

"My father was very involved in my life. I remember going to football games in the snow with him" is an example of memory associated with this part of the brain.

Medial Temporal Lobe

Working memory requires prefrontal cortex, dorsal thalamus, and this area of the brain.

Hippocampus

Asking a patient what they ate for breakfast tests for this.

Recent memory

This question evaluates immediate recall.

Can you repeat these six numbers?

Asking patient to remember 3 things and repeat them in a few minutes tests this.

Short term memory


**


This is the most reliable finding from CSF in MS during chronic progressive phase.

Oligoclonal Bands

**


This condition is the forerunner of MS


Transverse Myelitis


**


Acute onset of fever, sore throat, diplopia, dysarthria. Inflamed throat, left adductor palsy, impaired vertical pursuit, diffuse hyperreflexia w/ b/l clonus, LE spasticity, mild R hemiparesis. CT uninformative. CSF protein is 24, 10 mononuclear cells, glucose 70. Dx?


Multiple Sclerosis


**


Acute onset of pain and decreased vision in R eye. Colors look faded in R eye. On exam, R afferent pupillary defect and swollen R optic disc. Spontaneous recovery in 6 weeks. Pt likely to develop this later.


Multiple Sclerosis

**


25yo w/ diplopia, balance problems. On R lateral gaze, weakness of L medial rectus w/ nystagmus of R eye. On L lateral gaze, weakness of R medial rectus w/ nystagmus of L eye. Mild finger-nose ataxia. Dx?

Multiple Sclerosis
32yoF w/ vertigo and INO. Dx?

Multiple Sclerosis

***** *


Myasthenia gravis is associated with this EMG finding.


Decreased amplitude with repetitive motor nerve stimulation.

***** *


37yo truck driver w/ numbness of L hand increasing in severity over 2y. Reduced pinprick sensation on ring and pinky fingers. Atrophy of hypothenar muscle. Dx?


Ulnar Nerve Lesion

***


This is seen in electrophysiologic testing of patients with myasthenia gravis.


Decremental response to repetitive stimulation.

***


MOA of botulinum toxin at NMJ.


Inh of ACh release from presynaptic terminals

***


Myasthenia gravis can be dx in 80-90% of cases by identification of this serum Ab.


AChR


***


38yoF, pregnant Tri2, b/l hand numbness in thumb, forefinger, middle finger. Arms ache in morning from shoulders to hands. Dx?


Median Neuropathy at wrist

**
30yo develops pain behind L ear. Later complains of L face numbness, tearing, and discomfort w/ low frequencies. L weakness w/o sensory deficit. Dx?


Idiopathic Bell's Palsy
**
1mo s/p MVA, 21yo c/o persistent L shoulder/arm pain radiating to thumb. Weakness and decreased reflex of biceps. Dx?

C6 radiculopathy

**

Pt c/o progressive weakness for days. Exam shows generalized weakness and absent reflexes. Nerve conduction shows slowed velocities. Dx?

Acute polyneuropathy

**


65yo pt with progressive weakness worse w/ squatting and standing from chair. C/o decreased strength in R hand. Weak b/l quads and R thumb. Atrophy forearms w/ normal DTRs. Sensation intact, ROS neg. Normal CK, Jo1 Ab neg. Dx?


Myotonic Dystrophy

**


This chemo agent is most commonly associated with distal sensory polyneuropathy.

Cisplatin


**


Pt presents w/ personality changes, cognitive difficulty, affective lability, and olfactory and gustatory hallucinations. Most likely medical cause is this.


HSV Infection

Conduction block in NCS indicates this.

Focal demyelination

Polyneuropathy can be caused by deficiency or extreme excess of this B vitamin.
VitB6

57yo office worker w/ numbness in 4th/5th digit of R hand which wakes patient in middle of night. NCS will most likely find this.

Slowed conduction velocity across elbow in ulnar nerve.

45yo w/ LBP and R leg pain and numbness. Difficulty walking x4wk. R foot drop. NCS neg. EMG shows reduced recruitment and spontaneous activity in R tibialis anterior and posterior. Dx?

L5 radiculopathy
54yo c/o intermittent diplopia worsening over 3wk. Bilateral ptosis, mild esotropia, diplopia after maintaining upward gaze for 2 minutes. No dysarthria, 4/5 weakness in b/l proximal arm muscles. Most appropriate test?

Edrophonium
Which antibiotic is most likely to cause/precipitate acute myasthenia?

Ciprofloxacin
15yo h/o seizures starting @ 9yo followed by prolonged motor/sensory deficits lasting days to weeks. Pattern of deficits has changed over time. Hemicranial HA. No FamHx. Dxs?


Mitochondrial Encephalomyopathy,


Lactic Acidosis,


Stroke

Hyperextension lesion of shoulder results in weakness of abduction, internal rotation, flexion, and adduction of the extended arm. Nerve roots involved?

C5 and C6

55yoM h/o weakness and clumsiness. Sx began months ago w/ difficulty on fine motor tasks. Fasciculations of forearms w/ increased cramping. Diffuse wasting and weakness of BUE, fasciculations, slight spasticity on arms and legs, and hyperreflexia w/ extensor plantar responses. Senses, coordination, and CN exams wnl. Pathological process is occuring in these locations.


Ant Horn of SC,


Medial Brainstem,


Prerolandic cortex

13yoM w/ trouble in PE class. Symmetric weakness of BUE/BLE, worse in proximal muscles. Most prominent in quads/hams. Calves enlarged, painful w/ exercise. Serum CK is 13,000. Muscle bx shows abn dystrophin protein staining. Pathology has this pattern of inheritance.

X-Linked

Neoplasms of the thymus are associated with this.

Myasthenia Gravis

Hyperkalemic periodic paralysis is characterized by episodes of generalized weakness of fairly rapid onset. Also assoc w/ rise in K. Weakness typically appears after a period of rest after excercise. Disease is due to molecular deficits in this.

Na Channel Inactivation

PT was hit from behind while driving, woke w/ pain radiating into L ankle. Weakness of plantarflexion and decreased ankle jerk. Straight leg raising painful >45 degrees on L. Dx?

S1 Radiculopathy

Myasthenia gravis pt w/ mild respiratory infection develops severe respiratory fatigue, restlessness, and diaphoresis. Pt. appears anxious and tremulous. Tx?

Mechanical Ventilation

Pt w/ L foot drop. Weakness of dorsiflexion of L foot w/ small area of numbness in dorsum of L foot. Normal ankle, knee jerks, hamstring reflexes. Dx?

Peroneal Nerve Palsy

Ptosis, ipsilateral anhidrosis, conjunctival injection. Lesion is here.

Superior Cervical Ganglion

Most effective tx for spasmodic torticollis.

Botulinum Toxin

50yo secretary w/ cramping/stiffening of hands. Only while writing. Occasional hand tremor. Most effective therapy is this.

Botulinum Toxin

R neck pain, usually rotating neck to L. Corrected by touching chin. Spasm of R SCM on PE. Tx?

Botulinum Toxin

70yo w/ confusion, lethargy, fever. Dx of encephalitis is made after CSF. This clinical feature suggests West Nile.

Monoparesis

55yo c/o mild muscle ache and stiffness for which steroids were given. Hx of hyperlipidemia tx w/ atorvastatin and gemfibrozil w/ positive response. Serum CK is elevated. Dx?

Statin-Induced Myelopathy

63yo w/ insidious onset of neck pain, progressive limb weakness, falls, urinary incontinence. Decreased neck ROM, mild distal and prox limb weakness. Brisk DTRs with ankle clonus and upgoing plantar reflex. Increased muscle tone in legs. Dx?

Cervical Myelopathy


*****


Parkinson's Disease tx w/ levodopa. VH+. Recommend this.

Reduce dose of levodopa


***


Medication for orthostatic hypotension in Parkinson's.

Fludrocortisone


***


Postural instability, festination, truncal regidity. Lewy bodies visualized. Involuntary acceleration. Dx?

Parkinson's Disease


***


Picture showing substantia nigra changes. Dx?

Parkinson's Disease


***


New onset of pathological gambling, increased libido, hypersexuality in PD pt. Cause?

Pramipexole

80yoM w/ gait imbalance and falls. Kicks and screams while sleeping, dreams of being chased. Patient likely will develop this disease.

Parkinson's Disease

67yo w/ Parkinson's takes pramipexole for years w/o cognitive decline. Started gambling excessively, isn't drinking or using drugs. Likely cause?

Pramipexole

Most appropriate initial tx for idiopathic Parkinson's in an 81yo

Carbidopa/Levodopa

66yo c/o frequent falls, mild axial and LUE regidity. Mild slowness of finger tapping, hand opening, and wrist opposition (all worse on left). Normal posture. Slow gait w/ short steps, doesn't swing L arm. Slow rising from chair. Dx?

Parkinson's Disease

Implantation of deep brain stimulation electrodes is an effective tx for Parkinson's. This is the optimal location for electrodes.

Subthalamic Nucleus

DBS proble placement for primary generalized dystonia.

Globus Pallidus

Motor dysfunction in Parkinson's is due to this.

Increased activity in Subthalamic Nucleus and pars interna of Globus Pallidus

Characteristic of Parkinson's tremor.

Being inhibited with volitional movement.

Clinical syndrome that is most commonly comorbid with Parkinson's Disease.

Depression

This is typical of idiopathic Parkinson's disease rather than another parkinsonian syndrome.

Asymmetrical onset and progression of motor symptoms.

Patient with Parkinson's disease experiences visual hallucinations on levodopa/carbidopa therapy. This is the most appropriate intervention.

Quetiapine


***


26yo w/ sudden onset back pain. Spasms in R paraspinal muscles in lumbar region. Straight leg test is positive. Ankle jerk on L is diminished. No muscle weakness or sensory deficit. Next step.

MRI of lumbar spine

**

Contralateral loss of pain and temp sensation w/ motor paralysis and proprioception loss on the other. Dx?

Brown-Sequard Syndrome (Hemisection)

**


Subacute combined degeneration of posterior column of the spinal cord is 2/2 this deficiency.

Vitamin B12

T2 MRI in pt w/ cervical myelopathy. Dx?

Degenerative Cervical Spondylosis

New onset back pain after shoveling. L paraspinal muscle spasm, negative straight leg raise, reflexes symmetric. No weakness or sensory deficit. Management?

Conservative w/ NSAIDS

50yoM w/ acute neck pain radiating down L arm, gait problems, urinary incontinence. Which test?

MRI of C-Spine to r/o cord compression

23yoF f/u ER visit of sudden diplopia, R leg weakness and shaking, difficulty w/ speech resolving after hours. Had fever of 103.1 and was tx for UTI. Now has minimal R leg weakness, brisk DTR, and equivocal plantar reflex on R w/o other sx. Hx of multiple episodes like ER. CSF shows this.

Increase protein, Oligoclonal bands, increased nucleated cells