Brain lesions Flashcards
Visual problem in pituitary tumor compressing optic chiasm?
Bitemporal hemianopsia
Unsteady gait, appendicular ataxia in LE only and normal eye movement. Walks with ruching broad based gait
Cerebellar degeneration (alcoholic)
Severe occipital HA, BL papilledema. Chronic acne treated with isotretinoin. LP with elevated OP with no cells, glucose=62, protein=22. CT normal.
Psudotumor cerebri.
66 y/o with frequent falls, several month hx of anxiety, unwillingness to leave home. On exam, mild impairment of vertical gaze on smooth pursuit/ saccades, mild axial rigidity, and minimal rigidity of upper extremities, along with mild slowness of movement on finger tapping, hand opening, and wrist opposition. Posture nml. Gait tentative/ awkward, but w/o shuffling, ataxia, tremor. Pt is slow in arising from chair. Dx?
Progressive supra nuclear palsy.
79 y/o pt with deteriorating mental state over a 3 week period has an exaggerated startled response with violent myoclonus that is elicited by turning on the room lights, speaking loudly, or touching the pt. Myoclonic jerks are also seen. Dx
Spongiform encephalopathy
Pt presents with a slowly progressive gait disorder, followed by impairment of mental function, and sphincteric incontinence. No papilledema or headaches are reported. Likely dx?
Normal pressure hydrocephalus
65 yo pt fell several times past 6months. MSE nml. Smooth pursuit, saccadic movements impaired. Worse with vertical gaze. Full ROM with doll head maneuver. Mild symmetric rigidity/ bradykinesia, no tremor. MRI/CSF/labs unremarkable. Dx?
Progressive supra nuclear palsy.
28 y/o with emotional lability and impulsivity. LFTs elevated. Close relative had similar sx and died at 30 y/o from hepatic failure. Which blood levels would be dx?
Cerulopasmin.
Pt with acute onset of pain and decreased vision in the R eye. Colors look faded when viewed through the R eye. On exam, has a R afferent pupillary defect and a swollen right optic disc. Pt spontaneously recovers over the next 6 weeks. Likely to develop later?
MS
9 y/o F has 3 mo h/o seemingly unprovoked bouts of laughter. Worse when not sleeping well.Pt doesn’t feel happy during these episodes. Started menstruating 6 mo ago, at Tanner stage 4.Dx?
Hypothalamic hamartoma
5 y/o with 4 month story of morning hA, vomiting, and recent problems with gait, falls, and diplopia.
Medulloblastoma
70 y.o develops flaccid paralysis following severe water intoxication. He develops dysphagia and dysarthria without other CN involvement. Sensory exam is limited but grossly normal. DTRs are symmetric, and cognition is intact. Lively dx?
Central pontine myelin-lysis
Young adult gained 70 lbs in last year c/o daily severe headaches sometimes ass. with graying out of vision. Papilledema present. CT and MRI brain no abnormalities but ventricles smaller than usual. Goal of tx in this case?
Prevent blindness.
Superior homonymous quadratic defects in the visual fields result from lesions to which of the following structures?
Temporal optic radiations.
Tremor with frequency of around 3Hz, irregular amplitude, most evident towards end of reaching movements
Cerebellar tumor
Pt with several days of fever and severe HA, presents to ED b/o generalized seizure. Pt is confused and somnolent. Also reported to have been irritable and c/o foul smell. T2 MRQ displayed hyper intensity of left temporal.
Herpes encephalitis.
Acute onset of fever, sore throat, diplopia and dysarthria. Exam reveals an inflamed throat, left adductor nerve palsy w/ impairment of vertical pursuit diffuse hyperreflexia w/ bilateral clonus, lower ext spasticity, and mild R hemiparesis. Ct normal. CSF protein =24, mononuclear cells= 10, glucose= 70. Dx?
MS
Which is the most reliable finding from CSF analysis for a pt with MS in the chronic progressive phase of the disease?
Presence of oligoclonal bands
Benign intracranial HTN etiology
Hypervitaminosis A
Gait abnormality, slow movement, asymmetric UE rigidity. Difficulty in voluntary vertical upward/ downward gaze. Slowness/ rigidity improved slightly with levodopa. Later has problems with horizontal and vertical gaze. Oculocephalic reflexes normal. Involuntary saccades.
Progressive supra nuclear palsy.
Pt presents with personality changes, cognitive difficulties, affective lability, and olfactory and gustatory hallucinations. most likely medical cause?
HSV infection
What condition is a forerunner of MS?
Trasverse myelitis
Location of characteristic lesion seen in CT scans of pt with carbon monoxide poisoning associated comas?
Globus pallidus
Hx of dementia and myoclonus shows what pathologic changes in cresol violet changes
Cytosolic vacuolation of neuroglia with prion inclusions
What is the presentation expected with Wernicke’s encephalopathy?
Amnesia, confabulation, lack of insight
AIDS pt with new onset headache and cognitive decline, MRI shows multiple ring enhancing lesions. Cause?
Toxoplasmosis gondii
Neuropsychological test that examines both visual/spacial and executive functions?
Clock drawing
Imagine of a clock, with all the numbers drawn only on the R hand side, where is the lesion?
Parietal lobe
Head injury with personality changes, impulsivity, and euphoria. Site of injury?
Orbitofrontal cortex
What is the transmissible element that causes progressive decline and myoclonic jerks. Brain biopsy shows spongiform changes?
Prion
Kluver-Bucy syndrome: plasticity hyperorality, hyper sexuality, and hyperphagia, can be induced in animals with bilateral resection of which structure?
Temporal lobes
Most common psych complication from TBI
Depression
Executive dysfunction comes from damage to
Fronto-subcortical
36 y/o pt with double vision, vertigo, paresis of medial rectus on lateral gaze w coarse nystagmus in abducting eye w/lateral eye movement
MS
35 y/o pt w/ new onset headache, what suggests mass lesion with raised ICP?
Papilledema on eye exam
Aphasia secondary to lesion in posterior third of left superior temporal gyrus
Wernicke