Dementia Flashcards

(34 cards)

1
Q

What type of dementia?

medial temporal lobe atrophy (MTA) and parietal atrophy.

A

Alzheimer’s disease- AD

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2
Q

What type of dementia?

(asymmetric) frontal lobe atrophy and atrophy of the temporal pole.

A

Frontotemporal Lobar degeneration - FTLD

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3
Q

What type of dementia?

global atrophy, diffuse white matter lesions, lacunes and ‘strategic infarcts’ (infarcts in regions that are involved in cognitive function).

A

Vascular dementia

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4
Q

What type of dementia?

usually no specific abnormalities.

A

Dementia with Lewy bodies- DLB

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5
Q

The Global Cortical Atrophy is best assessed on this sequence:

A

FLAIR

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6
Q

The Medial Temporal Atrophy is best assessed on this sequence:

A

Coronal T1

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7
Q

Scoring system used i Parietal atrophy

A

Koedam score for Parietal Atrophy

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8
Q

Scaling system for WM lesions

A

Fazekas scale for WM lesions

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9
Q

list the Koedam score for PL atrophy

A

0- no atrophy
1 - Mild widening of posterior cingulate and Parietooccipital sulci
2- substantial
3 - extreme

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10
Q

FDG PET findings for AD

A

Hypo metabolism in TP lobe and or posterior cingulum

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11
Q

Ddx AD from FTD on PET

A

AD : affects TP lobe

FTD: FL

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12
Q

MTA is assessed on these features (3)

A
  1. Width of choroid fissure
  2. Width of temporal horn
  3. Height of Hippocampal formation
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13
Q

Name the drug that is used for treatment of vascular dementia/ LB dementia

A

cholinesterase inhibitors

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14
Q

T/F?

FLAIR is a good sequence to look at infratentorial region and for spinal cord

A

FALSE

LIMITED use of FLAIR in these areas- It suppresses signal from water as well as pathology with long T1 relaxation time.

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15
Q

The FTLD is formerly known as…

A

Pick’s disease

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16
Q

How would patients with FTLD present with?

A

behavioural and language disturbances

17
Q

What is an asymmetrical FTLD?

A

In Semantic dementia, an FTLD subtype with progressive aphasia and Left sided TL degeneration

18
Q

What conditions associated with Lewy body dementia (3)

A
  1. Atypical parkinson syndrome
  2. Progressive Supranuclear Palsy- PSP
  3. Multi System Atrophy- MSA
19
Q

How would patients with LB dementia present?

A
  1. Detailed visual hallucination
  2. Parkinson like symptoms
  3. Fluctuations in alertness and attention
20
Q

PSP

A

Part of atypical parkinsonian syndrome, with atrophy of midbrain
Upward gaze paralysis

Hummingbird sign

21
Q

MSA

A

Combination of :

  • Parkinsonian : MSA - P
  • Cerebellar : MSA - C
  • Pyramid
  • Autonomic dysfunction : MSA - A ( formerly known as Shy- Drager syndrome)
22
Q

MSA - A is formerly known as…

A

Shy Drager syndrome

23
Q

Sign associated with MSA- C

A

Hot Cross Bun sign-

24
Q

Re CJD

  • What is it caused by?
  • How do they present?
A

Caused by Prion

Present with progressive dementia leading to :

  • memory loss
  • personality changes
  • hallucination
25
Imaging CJD
Spongiform changes in the cortical and subcortical grey matter with loss of neurons and replacement by gliosis.
26
What sequence is used to detect CJD
DWI
27
Where is affected in mad cow disease?
posterior part of thalamus known as pulvinar
28
Corticobasal degeneration- CBD
cognitive dysfunction with parkinson like symptoms .
29
Typical manifestation of CBD
Alien hand syndrome
30
MRI findings in CBD
asymmetrical parietal cortical atrophy with associated hyper intensities of the WM on T2
31
Patients with huntingdon disease present with:
Early onset dementia Choreoathetosis Psychosis
32
Imaging features of Huntingdon disease
Atrophy of caudate nucleus and subsequent enlargement of the frontal horns of the LV
33
CADASIL
hereditary condition- progressive cognitive dysfunction; may present with migraine, stroke like episodes and behavioural disturbances.
34
Imaging features of CADASIL
WM hyper intensities in FL and anterior TL with lacunar infarcts