Intro to Neuropathology Flashcards

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1
Q

percentage of genes coding for nervous system-related proteins

A

50%

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2
Q

selective vulnerability of the hippocampus

A

hypoxic/ischemic changes

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3
Q

selective vulnerability of the caudate nucleus

A

Huntington’s disease

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4
Q

selective vulnerability of the motor neurons

A

amyotrophic lateral sclerosis (ALS)

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5
Q

selective vulnerability of substantia nigra

A

Parkinson’s disease

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6
Q

type of neurons most resistant to injury

A

astrocytes

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7
Q

selective vulnerability of oligodendria

A

myelin disorders

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8
Q

3 types of glial cells

A

astrocytes, oligodendocytes, ependymal cells (NOT microglia)

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9
Q

if needed, microglia can transform into ..

A

histiocytes

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10
Q

Nissl substances are representative of

A

rough endoplasmic reticulum

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11
Q

what part of the neuron stains with H&E?

A

nucleic acids

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12
Q

major mechanisms of cellular injury

A

free radical injury, excitotoxic injury

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13
Q

examples of excitotoxic injury

A

glutamate, aspartate; depolarization; NMDA amino acid receptor

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14
Q

*what is the mechanism of excitotoxic injury?

A

injured neurons release their excitatory NTs (glutamate), which results in depolarization of the surrounding neurons through the inappropriate activation of NMDA receptors

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15
Q

how can you protect against excitotoxic injury?

A

antioxidants

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16
Q

excitotoxic injury via NMDA receptors results in..

A

calcium influx that interferes with mitochondrial function which eventually leads to cell death

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17
Q

characteristics of acute neuronal injury

A

eosinophilic necrosis (red), hypoxic injury, shrunken cytoplasm, dark smudgy chromatin, irreversible cell death

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18
Q

how long does it take for acute neuronal injury to show up on light microscopy?

A

12 hrs

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19
Q

hippocampus CA1 region (Sommer’s sector) is most sensitive to what type of injury?

A

hypoxic-ischemic

20
Q

subacute and/or chronic type of neuronal injury

A

degeneration

21
Q

the changes that occur in the neuron body in response to axonal injury is termed..

A

axonal reaction (formerly known as central chromatolysis); regenerative attempt

22
Q

examples of axonal reaction

A

damage to axon, margination of Nissl substance, central clearing of the cytoplasm, peripheral displacement of the nucleus, rounding of the cell body

23
Q

term for when an axon is transected, and the proximal portion starts to regenerate and myelinate

A

Wallerian degeneration

24
Q

if the BM is not intact during Wallerian regeneration, what is the outcome?

A

chaotic proliferation of axons, resulting in a painful nodule called traumatic or amputation neuroma

25
Q

how are neuromas treated?

A

can be anastomosed to facilitate healing, or if damage is extensive, nerve transplantation can be done

26
Q

what are axonal spheroids and how do they form?

A

when an axon is transected, the transport material going towards the synapse will accumulate at the site of injury

27
Q

identification of axonal spheroids on path slides is important because..

A

it helps confirm presence of an infarct next to them; also in the diagnosis of such things as diffuse axonal injury

28
Q

stain used to highlight axonal spheroids/swelling

A

silver stains

29
Q

most common neuronal inclusion

A

viral inclusion

30
Q

a neuronal inclusion seen with Parkinson’s disease pathology

A

Lewy body

31
Q

inclusion seen in Pick’s disease/frontotemporal lobar degeneration

A

Pick’s body

32
Q

inclusion seen in alzheimer’s

A

neurofibrillary tangles (accumulate in the cytoplasm)

33
Q

what is trans-synaptic degeneration?

A

secondary degeneration of a neuron connected to a dying neuron; can be counter-intuitive; anterograde or retrograde

34
Q

what physically happens to astrocytes when they react?

A

develop plump cytoplasm, processes become more prominent; indicates some pathology

35
Q

inclusions representative of a hyperammonemia typically seen with cirrhosis

A

Alz type II glia (astrocytes)- nothing to do with Alz

36
Q

astrocyte pathology typically seen with demyelinating diseases like MS

A

Creuzfeldt astrocyte

37
Q

neuronal inclusion made of GFAP and B-crystalline

A

Rosenthal fibers (slow-progressing, in the cytoplasm)

38
Q

fried egg appearance

A

oligodendrocytes

39
Q

oligodendrocyte inclusions are seen in this disease

A

progressive multifocal leukoencephalopathy

40
Q

the diagnostic value of oligodendrogial changes

A

satellitosis around neurons and blood vessels by the neoplastic cells infiltrating grey matter areas.

41
Q

two major changes associated with reactive microglia & what they’re associated with

A

microglial nodules, neuronophagia; most commonly associated with viral infections of the CN

42
Q

PNS biopsies are usually taken from the..

A

sural nerve (entirely sensory)

43
Q

pathologic characteristic of Charcot-Marie-Tooth disease

A

“onion bulb” Schwann cell in the PNS resulting from constant remyelination and demyelination

44
Q

technique using chemical reactions to highlight certain tissue components like mucin, myelin, collagen

A

histochemistry

45
Q

special staining technique for astrocytes using antibodies raised against specific components of cells

A

immunohistochemistry

46
Q

in-situ hybridization is used to show the presence of

A

DNA segments