Neuro Flashcards

1
Q

functions of the CNS are performed by two types of cells

A

neurons and glia

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2
Q

cells that transmit signals between each other and from one part of the body to another

A

neurons

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3
Q

cells abundant in the gray matter

A

neurons

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4
Q

cells that regulate homeostasis and provide support and protection of neurons

A

glia

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5
Q

cells abundant in white matter

A

glia

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6
Q

maintains the blood brain barrier by controlling level of NTs around synapses and regulating ions and providing metabolic support

A

astrocytes

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7
Q

myelinates CNS axons, providing structural framework

A

oligodendrocytes

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8
Q

involved in brain’s immune system as phagocytes

A

microglia

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9
Q

lines the spinal cord and ventricles to produce CSF

A

ependymal cells

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10
Q

neural injury in the absence of glucose or oxygen/traumatic injury

A

acute rapid process

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11
Q

neural injury associated with the accumulation of protein aggregates/proteinopathies

A

slow, degenerative process

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12
Q

red neurons indicate

A

acute neural injury

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13
Q

most important histopathologic marker of CNS injury

A

gliosis

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14
Q

hypertrophy and hyperplasia of astrocytes

A

gliosis

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15
Q

thick, elongated brightly eosinophilic structures within astrocytes as a result of long standing gliosis

A

Rosenthal fibers

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16
Q

polyglucosan aggregates from waste products

A

corpora amylacea

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17
Q

corpora amylacea is also known as

A

brain sand

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18
Q

microglia congregating around cell bodies of dying neurons

A

neuronophagia

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19
Q

aggregates around small foci of tissue necrosis in microglial injury

A

microglial nodules

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20
Q

4 responses of microglia to injury

A

-proliferation
-forms elongated nuclei (rods)
-forms microglial nodules
-neuronophagia

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21
Q

injury induced by acquired demyelinating disorders and leukodystrophies

A

oligodendrocyte injury

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22
Q

may produce extensive ependymal injury with viral inclusions

A

CMV

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23
Q

small irregularities on the ventricular surfaces

A

ependymal granulations

24
Q

3 causes of increased intracranial pressure

A

-generalized brain edema
-increased CSF volume
-expanding mass lesion

25
an increase in extracellular fluid caused by blood-brain barrier disruption and increased vascular permeability
vasogenic edema
26
an increased in intracellular fluid secondary to neuronal, glial, or endothelial cell membrane injury
cytotoxic edema
27
two pathways of cerebral edema
vasogenic and cytotoxic edema
28
seen with generalized hypoxic or ischemic insult with a metabolic derangement that prevents maintenance of the normal ion gradient (obesity/diabetes)
cytotoxic edema
29
edema that involves both cortical grey and white matter
cytotoxic edema
30
edema confined to white matter with fingerlike projections extending in subcortical white matter
vasogenic edema
31
3 changes associated with generalized edema
- flattening of gyri - narrowing of sulci - compression of ventricular cavities
32
most occur as a consequence of impaired flow and resorption of CSF
hydrocephalus
33
overproduction of CSF is more typical of tumors of the
choroid plexus
34
compensatory increase in ventricular volume secondary to a loss of brain parenchyma
hydrocephalus ex vacuo
35
hydrocephalus ex vacuo is common in this disease
Alzheimer's
36
herniation is mostly associated with
mass effect
37
unilateral or asymmetric expansion of a cerebral hemisphere causing displacement of the cingulate gyrus under the falx
subfalcine herniation
38
can lead to compression of the anterior cerebral artery and its branches
subfalcine herniation
39
medial aspect of temporal lobe is compressed against the free margin of the tentorium
transtentorial/uncal herniation
40
hemorrhagic lesions seen in uncal herniations
Duret hemorrhages
41
displacement of cerebellar tonsils through foramen magnum
tonsillar herniation
42
defects that account for most CNS malformations
neural tube defects
43
the most common neural tube defects involve the
spinal cord
44
well known risk factor for neural tube defect
folate deficiency
45
most common neural tube defect
spina bifida occulta
46
deficiency of the occipital bone with cervicothoracic spinal fusion
iniencephaly
47
combination of anencephaly with contiguous bony defect of the spine
craniorachischisis
48
microcephaly can be caused by these three things
-chromosome abnormalities -fetal alcohol syndrome -HIV infection in utero
49
posterior fossa anomaly associated with spina bifida
arnold-chiari type II malformation
50
small posterior fossa with a misshaped midline cerebellum with downward extension of vermis through foramen magnum
arnold-chiari type II malformation
51
hydrocephalus and lumbar myelomeningocele result from
arnold-chiari type II malformation
52
less severe posterior fossa anomaly with low lying cerebellar tonsils that extend into the vertebral canal
chiari type I malformation
53
enlarged posterior fossa with absent/scant cerebellar vermis that is replaced by midline cysts contiguous with leptomeninges
Dandy-Walker malformation
54
nonprogressive neurologic motor deficit due to insults in prenatal and perinatal periods of development
cerebral palsy
55
infarcts in the periventricular white matter
periventricular leukomalacia
56
extensive ischemic damage causing large destructive cystic lesions to develop throughout the hemispheres
multicystic encephalopathy
57