10.20 Cellular Neuropathology Lect + Lab Flashcards

1
Q

what is the mechanism for diabetic neuropathy? _________ and _________ factors

A

metabolic

vascular

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2
Q

___________ causes glycosylation end products, causing thickening of _________ ___________ around small capillaries. What does this impair?

A

hyperglycemia
basement membrane
exchange of nutrients and oxygen

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3
Q

what is a concern with diabetic neuropathy?

A

because of loss of sensation in distal areas, you can get wounds and not notice and then there is not a good blood supply and they can get infected

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4
Q

is Guillan Barre CNS or PNS? what is it caused by/usually seen after?

A
demyelination disease of the PNS
immune mediated (T-cells post acute flu-like illness)
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5
Q

the _________ in Guillan Barre are sensitized to ___________ _______ ________

A

T-cells

peripheral nerve myelin

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6
Q

clinically, what do you see with Guillan Barre?

A

ascending paralysis

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7
Q

chronic inflammatory demyelinating polyraiculoneuropathy (CIPD) shows under histology as multiple _____________. Why?

A

onion bulb formations

repeated demyelination and remyelination

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8
Q

when does segmental demyelination occur?

A

when there is dysfunction of the Schwann cell or damage to the myelin sheath

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9
Q

what can segmental demyelination look like in histology if it is recurrent or persistent?

A

onion bulb formation

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10
Q

the variation in neuronal damage in different pathological states is termed

A

selective vulnerability

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11
Q

what are two examples of selective vulnerability? (cases)

A
  1. hypoxia

2. degenerative diseases of the NS

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12
Q

in hypoxic encephalopathy, which neurons are selectively vulnerable?

A
  1. purkinje cells of the cerebellum
  2. Sommer’s sector of the hippocampus
  3. deeper layers of the cerebral cortex
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13
Q

what happens to the cell when it suffers from an irreversible ischemic injury (histologically)?

A

it gets eosinophilic (red = dead)

the chromatin fades

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14
Q

what is gliosis?

A

proliferation of astrocytes and astrocytic processes in response to injury

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15
Q

when an astrocyte is enlarged and has a homogeneous pink-staining cytoplasm as a response to injury, what is it called?

A

gemistocytic astrocyte

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16
Q

what causes multiple sclerosis? is it in the CNS or PNS?

A

it is in the CNS

autoimmune

17
Q

in MS plaques _________ are destroyed and the ________ has degenerated

A

oligodendrocytes

myelin

18
Q

where is a characteristic location for an MS plaque?

A

around the ventricles

periventricular white matter

19
Q

what causes progressive multifocal leukoencephalopathy (PML)? Is it in the PNS or CNS?

A

an opportunistic infection (JC virus) in immune compromised patients

in the CNS

20
Q

what does the JC virus destroy in people with PML?

A

oligodendrocytes

21
Q

histologically, there are abnormal ____________ in people with PML

A

astrocytes

22
Q

how can you tell the difference between a gemistocytic astrocyte and a macrophage?

A

well circumsized border - macrophage

23
Q

is Guillan Barre PNS or CNS?

A

PNS

24
Q

onion bulb formation is a hallmark of ____________ and ____________

A

demyelination
demyelination
(CHRONIC)

25
Q

Tay Sachs disease is a neuronal ____________. Thus, what do the neurons look like?

A

storage

massive

26
Q

dark nuclei - large that look like they used to be oligos in progressive multifocal leukoencephalopathy:

A

JC virus infected oligos