Neuro - Pathology (Dementia) Flashcards

Pg. 483 in First Aid 2014 Sections include: -Dementia

1
Q

What is dementia?

A

A decrease in cognitive ability, memory, or function with intact consciousness

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2
Q

What is the most common cause of dementia in the elderly? Besides the elderly, which patient population has an increased risk of developing this?

A

Alzheimer disease; Down syndrome patients have an increased risk of developing Alzheimer

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3
Q

What percentage of Alzheimer disease is associated with its familial form? With what kind of proteins is this form associated with in general, early onset, and late onset?

A

Familial form (10%) associated with the following ALTERED proteins (respective chromosomes in parentheses): EARLY ONSET - APP (Chr 21), presenilin-1 (Chr 14), presinilin-2 (Chr 1); LATE ONSET - ApoE4 (Chr 19)

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4
Q

What protein is protective against Alzheimer disease, and on what chromosome is it found?

A

ApoE2 (Chr 19) is protective

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5
Q

What are 2 gross findings in Alzheimer disease?

A

(1) Widespread cortical atrophy (2) Narrowing of gyri and widening of sulci

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6
Q

Which neurotransmitter is decreased in Alzheimer disease?

A

Decreased ACh

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7
Q

What are 2 histological findings characteristic of Alzheimer disease?

A

(1) SENILE PLAQUES (2) NEUROFIBRILLARY TANGLES

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8
Q

What is the structure of Senile plaques? What is a complication that can arise from them? How are they synthesized?

A

SENILE PLAQUES: extracellular Beta-amyloid core; may cause amyloid angiopathy –> intracranial hemorrhage; ABeta (amyloid-Beta) synthesized by cleaving amyloid precursor protein (APP)

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9
Q

What is the key structure/component of Neurofibrillary tangles? What clinical significance do they have?

A

NEUROFIBRILLARY TANGLES: intracellular, hyperphosphorylated tau protein = insoluble cytoskeletal elements; Tangles correlate with degree of dementia

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10
Q

Name 4 major causes of dementia. What are 6 other causes?

A

(1) Alzheimer disease (2) Pick disease (frontotemporal dementia) (3) Lewy body dementia (4) Creutzfeldt-Jakob disease (Note - Other causes of dementia include: (1) multi-infarct, (2) syphilis, (3) HIV, (4) vitamins B1, B3, or B12 deficiency, (5) Wilson disease, and (6) NPH)

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11
Q

What is another name for Pick disease? What 4 symptoms/aspects of the disease?

A

Pick disease (frontotemporal dementia); (1) Dementia (2) Aphasia (3) Parkisonian aspects (4) Change in personality

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12
Q

What portion(s) of the brain is (are) spared in Pick disease?

A

Spares parietal lobe and posterior 2/3 of superior temporal gyrus (hence name frontotemporal dementia)

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13
Q

What is a histological finding associated with Pick disease? What is its gross finding?

A

Pick bodies: spherical tau protein aggregates; Frontotemporal atrophy

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14
Q

What is the initial presentation of Lewy body dementia and its progression of symptoms?

A

Initially dementia and visual hallucinations followed by parkisonian features

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15
Q

What is the defect in Lewy body dementia?

A

alpha-synuclein defect

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16
Q

What are the symptoms and time course of Creutzfeldt-Jakob disease?

A

Rapidly progressive (weeks to months) dementia with myoclonus (“startle myoclonus”)

17
Q

What is a gross finding associated with Creutzfeldt-Jakob disease? What is the underlying molecular change?

A

Spongiform cortex; Prions (PrP^c –> PrP^sc [Beta-pleated sheet resistant to proteases]

18
Q

What is the 2nd most common cause of dementia in elderly?

A

Multi-infarct