Congenital Abnormalities - Neuro Flashcards

(51 cards)

1
Q

pale areas in neuronal cytoplasm from dispersion of Nissl’s substance

A

chromatolysis

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2
Q

loss of myelination with preservation of the cell body and axon

A

demyelination

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3
Q

selective degeneration of myelin sheaths with axon intact

A

1 demyelination

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4
Q

mechanisms of 1 demyelination

A

inherited enzyme defects
impaired synthesis
cytotoxic edema
destruction of myelin by metabolites
immunologic

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5
Q

1 demyelination - inherited enzyme defect

A

leukodystrophy

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6
Q

1 demyelination - impaired myelin synthesis and maintenance

A

viral infection
nutritional deficiency
toxins

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7
Q

1 demyelination - cytotoxic edema

A

status spongiosus

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8
Q

1 demyelination - destruction of myelin by metabolites

A

lysolecithin

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9
Q

1 demyelination - immunologic

A

cell mediated

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10
Q

consequence of primary destruction with the loss of axon and not selective injury of myelin sheath

A

2 demyelination

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11
Q

pale, swollen fibers (+/- axonal loss)

A

axonal degeneration

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12
Q

destruction of axon and myelin sheath following trauma or toxic injury

A

wallerian degeneration

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13
Q

accumulation of glial cells around damaged neurons

A

satellitosis

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14
Q

macrophagic phagocytosis of necrotic neurons

A

neuronophagia

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15
Q

microglial proliferation (viral infection)

A

microgliosis

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16
Q

astrocytic proliferation in damaged areas

A

astrocytosis

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17
Q

accumulation of leukocytes in perivascular spaces

A

perivascular cuffing

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18
Q

softening and liquefaction of nervous tissue from necrosis of neurons and glial cells

A

malacia

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19
Q

rare or cysts are found where nervous tissue was destroyed

A

scar formation

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20
Q

eosinophilic; usually single and displaces the nucleolus with a clear halo specific for viral infections

A

intranuclear inclusion bodies

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21
Q

eosinophilic with internal granules which stain purple specific for rabies

A

intracytoplasmic
(Negri bodies)

22
Q

neural tube closure defects

23
Q

total absence of the entire brain even though a small portion of the brain persists
(medulla / mesencephalon)

24
Q

anencephaly lesions

A

absence of cerebral hemispheres
failure of forebrain fusion

25
failure of bilateral separation of the primitive single telencephalic cavity into 2 hemispheres common in pigs and lambs
prosencephalic hypoplasia
26
lesions of prosencephalic hypoplasia
single central ventricle absence of the longitudinal fissure, corpus callosum, olfactory bulb + optic tract BRAIN STEM NORMAL
27
protrusion of the brain through a defect in the cranium (cranium bifidum)
meningoencephalocele and cranium bifidum
28
protrusion of the meninges - fluid-filled
meningocele
29
dorsal defect in closure of one or several vertebral arches that form the dorsal spinal column covering the spinal cord
meningomyelocele and spina bifida
30
sequelae of meningomyelocele or spina bifida
meningocele meningomyelocele
31
occurs most frequently in brachycephalic breeds of dogs is inherited in Manx cats
spina bifida / sacrococcygeal agenesis
32
abnormal dilation of the central canal of the spinal cord / infectious or genetic injury
congenital hydromyelia
33
obstruction of the central canal CSF flow due to infection, inflammation and neoplasia
acquired hydromyelia
34
absence of primary gyri - "smooth brain" -- due to defective neuronal migration
lissencephaly (agyria)
35
2 types of encephaloclastic defects
porencephaly (focal) hydranecephaly (diffuse)
36
cysts or cavities in the white matter walls of the cerebral hemisphere causing cystic cavitation of the brain
porencephaly
37
complete or almost complete absence of the cerebral hemispheres in a brain of normal size and formation most common in calves with cerebellar hypoplasia
hydranencephaly
38
slight to marked decrease in size of cerebellum or stump of tissue commonly seen in dogs/cats/ calves following intra-uterine viral infections or inherited
cerebellar hypoplasia
39
tubular cavitation of the spinal cord over several segments leaving the animal unable to completely extend the hind limbs, normal posture or attitude is crouched with symmetrical hopping gait at 8 months of age
syringomyelia
40
simple dilatation of the central canal of the spinal connected with the central canal and lined by ependymal cells
hydromyelia
41
abnormal accumulation of fluid in the ventricles of the brain and sub-meningeally common in brachycephalic breeds
hydrocephalus
42
type of hydrocephalus with fluid accumulating in the ventricles
internal hydrocephalus
43
type of hydrocephalus with fluid accumulating in the sub-arachnoid space
external hydrocephalus
44
type of hydrocephalus with fluid accumulating in both ventricles and sub-arachnoid space
communicating hydrocephalus
45
causes of congenital hydrocephalus
idiopathic intra-uterine viral infections nutritional deficiencies malformation of the cranium
46
consequence of a periductal gliosis of the aqueduct of Sylvius
congenital hydrocephalus
47
lesions of congenital hydrocephalus
dilated ventricles or duct system dome-shaped, thin-boned and enlarge cranium
48
obstruction of flow due to an accumulation of and organization of exudate commonly as an internal hydrocephalus with no malformation of the cranium
acquired hydrocephalus
49
causes of acquired hydrocephalus
bacterial meningitis granulomatous meningitis intracranial neoplasms parasitic cysts cholesteatoma (horses)
50
lesions of acquired hydrocephalus
pressure atrophy of the septum pellucidum and hippocampus with ventricular dilatation and atrophy of cerebrocortical white matter *may be difficulat to see in neonates*
51