Dementia, Cohen II Flashcards

1
Q

multi infarct dementia

A

clincally Hx stokes and hemorrhagic strokes

Step like downhill course

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2
Q

clinical findings multi infarct dementia

A

focal findings on exam: aphasia, dysarthria, hemiparesis, spasticity, visual field cuts

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3
Q

seizures are more common in what type dementia

A

multi infarct

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4
Q

likely concurrent comorbidities in multi infarct dementia

A

coronary artery disease
peripheral vascular disease
carotid stenosis

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5
Q

What are risk factors for multi infarct dementia

A
HTN
DM
HLD
obesity, inactivity
smokers, alcohoics
known CAD, or Afib
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6
Q

Tx of those at higher risk for multi infarct dementia

A

control risk factors
aspiring and other inhibitors of platelet aggregation
anti coagulants

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7
Q

Fronto-temporal Lobar Dementia

A

family of multiple disorders with dementia

decline in behavior and speech!!

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8
Q

autopsies and MRI of fronto-temporal lobar dementia

A

visible degeneration of frontal lobes and anterior temporal lobes!! MRI!!
increased tau!
TDP43!! and ubiquitin!!
M=W

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9
Q

onset fronto temporal lobar degeneration

A

younger than AD
50s early 60s
“Picks”

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10
Q

Dx frontotemporal dementia

A

MRI! frontal and anterior temporal lobe degeneration

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11
Q

clinical features frontotemporal dementia

A

major personality changes like inappropariate actions, apathy, loss sexual inhibitions no concern appearance
shoplifting!
no ability to plan acitivites
become obsessed with certain subjects, clap hands inappropriately
over eat over drink

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12
Q

frontotemporal dementia similar to what

A

ALS patients

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13
Q

memory loss in frontotemporal dementia

A

later on

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14
Q

Language form of frontotemporal dementia

A

progressive aphasia like Brocas
L hemisphere more atrophy than R
sentences shorter and shoter with progressive inability to name and read and write

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15
Q

how to Dx frontotemporal dementia clinically

A
say things totally irrelevant
cannot name subject
gait ataxia
slow movements
poor decision making
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16
Q

what tx help in frontotemporal dementia

A

antidepressants

sometimes antipsychotics

17
Q

What is Transmissible Spongiform Encephalopathy

A

CJD from prions

18
Q

what is prion

A

proteinaceous particles that can reporduce without nucelic acids

19
Q

progression CJD

A

rapid dementia over 1 year
prominent myclonic jerks
loss of balance and coordination, mildy extrapyramidal and sometimes cerebellar signs
occasionally familial

20
Q

Dx CJD

A

rapid downhill course
EEG triphasic waves
CSF: high levels 14-3-3 protein

21
Q

MRI CJD

A

rapidly accumulating subcortical deposits in cerebral hemispheres and cerebellar deposits sometimes

22
Q

brain Bx of CJD

A

prions and spongiform changes with loss of neurons and gliosis

23
Q

triad signs of normal pressure hydrocephalus

A

gait disturbance
incontinence
dementia
Wet Wide Weird

24
Q

1st sign normal P hydrocephalus

A

gait disturbance

wide based

25
Q

type of dementia in normal P hydrocephalus

A

decreased attention space
mental slowing
disorientation, confusion
depression

26
Q

MRI in normal P hydrocephalus

A

huge ventrilces

less prominent sulci

27
Q

Tx Norm P hydrocephalus

A

take off CSF like 20-30 cc