Neuropathology Flashcards

(53 cards)

1
Q

When are balloon cells and Hirano bodies seen together?

A

Pick’s disease

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2
Q

What happens to frontal and temporal lobes in Pick’s disease?

A

Asymmetrical atrophy

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3
Q

What are pick cells?

A

Swollen cortical pyramidal cells

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4
Q

What is the spongiform encephalopathy secondary to in CJD?

A

Neutropil vacuolation

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5
Q

Protective factor against Alzheimer’s dementia

A

Smoking
NSAIDs
Oestrogen
Premorbid intelligence and education

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6
Q

Macroscopic changes in Alzheimer’s

A

Enlargement of lateral and 3rd ventricles
Global brain atrophy
Reduction in brain weight
Sulcal widening

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7
Q

Microscopic changes in cerebral cortex in Alzheimer’s

A
Neuronal loss
Senile plaques
Neurofibrillary tangles
Reactive astrocytosis
Shrinking of dendritic branching
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8
Q

Stain used in detection of Pick bodies

A

Anti-tau antibodies

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9
Q

Which memories are lost in dissociative amnesia?

A

Loss of memory of personal events well rehearsed

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10
Q

Histological changes of dementia pugilistica

A

Neuronal loss

Neurofibrillary tangles

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11
Q

Macroscopic changes in dementia pugilistica

A

Thinning of corpus callosum
Perforation of septum pellucidum
Ventricular enlargement

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12
Q

What are lewy bodies made of?

A

Alpha synuclein

Ubiqutin

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13
Q

What are lewy bodies made of?

A

Alpha synuclein

Ubiqutin

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14
Q

Where would you find the degenerative changes associated with Wernicke’s encephalopathy?

A

Gliosis and small haemorrhages in structures surrounding the third ventricle and aqueduct - mamillary bodies, hypothalamus, mediodorsal thalamic nucleus, colliculi and midbrain tegmentum

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15
Q

Findings in CSF of somebody with Alzheimer’s

A

Reduced beta-amyloid
Increased tau and phosphorylated tau
Increased tau-to-amyloid ratio

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16
Q

MRI findings of somebody with aggression and stereotyped motor behaviour

A

Hypoplastic cerebellum

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17
Q

What are hirano bodies made of?

A

Intracellular aggregates of actin and actin-associated proteins

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18
Q

What is Binswanger’s disease?

A

Subcortical vascular dementia

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19
Q

What is Binswanger’s characterised by?

A

Presence of many small infarctions of the white matter that spares the cortical regions

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20
Q

Is there correlation between number of lewy bodies and cognitive decline?

A

There is no simple correlation

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21
Q

Which antibody could be used to identify Lewy bodies?

A

Antibody to protease ubiquitin

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22
Q

What stain could you use to identify lewy bodies?

A

Antibodies to alpha-synuclein

23
Q

What are lewy body neurites?

A

Nerve cell processes that contain alpha-synuclein

24
Q

List 5 tauopathies

A
  1. AD
  2. Pick’s disease
  3. PSP
  4. Corticobasal degenerations
  5. Frototemporal dementia with parkinsonism
25
List 3 synucleinopathies
1. PD 2. DLB 3. MSA
26
Most common type of frontotemporal dementia
Frontal lobe degeneration type
27
Pathology of frontal lobe degeneration of FTD
Spongiform degeneration or microvacuolation of the superficial neutropil seen chiefly in layers III and V of the cortex
28
Loss of which type of cells occurs in frontal lobe degeneration type of FTD
Large cortical nerve cells | Minimal gliosis
29
How is Pick's disease characterised?
Preponderance atrophy in the frontotemporal regions
30
What are the 3 types of FTD?
1. Frontal lobe degeneration type 2. Pick's type 3. Motor neurone disease type
31
What are Pick's bodies?
Masses of cytoskeleton elements
32
What are Pick's cells?
Abnormal swollen oval-shaped neuronal cells with loss of Nissl's substance and peripherally displaced nucleus
33
Pathology associated with Pick's type FTD
Loss of large cortical cells Abundant gliosis Pick's bodies
34
How does MND type of FTD differ from the others?
Cerebral atrophy is less marked
35
What are the 3 forms of CJD?
1. Sporadic 2. Familial 3. Variant
36
What type of CJD is related to bovine spongiform encephalopathy?
Variant
37
Microscopic pathology of CJD
Spongiform encephalopathy secondary to neutropil vacuolisation
38
Where is prion protein coded?
Chromosome 20
39
Which stain can be used to identify prion protein?
Immunoperoxidase
40
What is there accumulation of in vCJD?
Prion protein
41
What is the best test for vCJD?
MRI
42
Features of classic CJD - age & course
Elderly | Short course
43
Is pulvinar sign seen in classic CJD?
No
44
In which type of CJD can prion protein be isolated from tonsillar tissue?
vCJD
45
What is the most common psychiatric presentation in AIDS?
HIV-related dementia
46
Where is the primary auditory cortex?
Heschl's gyrus
47
What gross pathological changes occur in the brain in schizophrenia?
Brain weight, length and volume of cerebral hemispheres decrease
48
What enlarges in the brain in schizophrenia?
Lateral ventricles
49
What would reduced in the parahippocampla gyrus or hippocampus?
White matter
50
What histological changes would you see in schizophrenia?
Reduced cell numbers or cell size in hippocampus and DLPFC
51
MRI in bipolar and unipolar mood disorders
White matter hyperintensities particularly in deep subcortical white matter
52
Which group of people with mood disorders are white matter hyperintensities most associated?
Elderly - linked to risk factors for vascular disease
53
In terms of prognosis, what do white matter hyperintensities suggest?
Poor prognosis