CNS Flashcards

(61 cards)

1
Q

neural tube defect: no cerebral hemispheres

A

anencephaly

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2
Q

neural tube defect: meninges and brain don’t close

A

encephalocele

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3
Q

neural tube defect: meninges don’t close

A

cranial meningocele

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4
Q

neural tube defect: meninges and spinal cord; spina bifida

A

meningomyelocele

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5
Q

neural tube defect: meninges; spina bifida

A

spinal meningocele

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6
Q

neural tube defect: vertebral arches do not close; no herniation; hairy patch

A

spina bifida occulta

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7
Q

disorders of forebrain development: brain is not divided hemispheres

A

holoprosencephaly

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8
Q

holoprosencephaly can result in …

A

cyclopia

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9
Q

disorders of forebrain development: many small gyri

A

polymicrogyria

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10
Q

disorders of forebrain development: no gryation

A

lissencephaly

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11
Q

disorders of forebrain development: brain cells not divided in organized layers

A

cerebral cortical dysplasia

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12
Q

“water on the brain” -too much CSF for whatever reason. usually obstruction in flow

A

hydrocephalus

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13
Q

posterior skull too small, structures impede CSF flow

A

Arnold-Chiari malformations

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14
Q

cystic cerebellar vermis (the middle part) causes outflow obstruction of CSF

A

Dandy-Walker malformation

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15
Q

also known as “Phakomatoses”; malformations and non-neoplastic and neoplastic growths of nervous system, skin, and other systems

A

neurocutaneous syndromes

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16
Q

gliomas and meningiomas; NF1 tumor suppressor gene; cafe au lait; lisch nodule

A

neurofibromatosis I

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17
Q

germinal matrix hemorrhage- common in extreme …

A

prematurity

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18
Q

usually idiopathic, but can be caused by an assault on the brain (metabolic, infectious, trauma); lesion is often in temporal lobe; causes periods of clonus with unconsciousness

A

epilepsy

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19
Q

increased ICP; blood-brain barrier not intact; fluid seeps out of vessels; little lymphatic drainage

A

vasogenic cerebral edema

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20
Q

increased ICP: cells themselves swell with fluid due to injury

A

cytotoxic cerebral edema

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21
Q

increased ICP: cerebrum slips under the “falx”-a fold of dura at the top

A

subfalcine herniation

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22
Q

increased ICP: cerebrum slips under the “tentorium cerebelli”-a fold of dura at the sides, also known as “Uncal” from the actual area that is affected

A

transtentorial herniation

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23
Q

increased ICP: tonsils of cerebellum slip through foramen magnum

A

tonsillar herniations

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24
Q

Increased ICP: buildup of the CSF in ventricles, typically due to decreased outflow

A

hydrocephalus

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25
in hydrocephalus: if cranial sutures are fused, results in ...
big ventricles and compressed brain matter
26
in hydrocephalus: if sutures are open, results in ...
increased head size
27
one treatment strategy for hydrocephalus is ... where a conduit is placed into the ventricles to drain fluid, either to an outside container or to peritoneal cavity in the abdomen
shunting
28
most due to atherosclerotic vascular disease; blurring between gray and white matter; red dead neurons; gliosis
cerebral infarcts
29
perfusion to entire brain is inadequate; results in ischemia
global hypoxic-ischemic encephalopathy
30
most common reason for intracranial hemorrhages
hypertension
31
likely due to acquired weakening in wall; found in circle of willis; most at bifurcations; can cause subarachnoid hemorrhage;
saccular (or berry) aneurysms
32
patients experience a pass out -> "lucid interval" -> rapid decompensation; often caused by rupture of middle meningeal artery with accompanying skull fracture; characteristic "lens" shape on CT scan; requires emergent drainage
epidural hematoma
33
acute or chronic; not a dramatic because of slower venous bleeding rate; often occurs in elderly and may be diagnosed as dementia; "crescent" shaped bleeding
subdural hematoma
34
characteristic whiplash motion: auto accident; axonal swellings: spheroids
diffuse axonal injury
35
contusion: the actual impact
coup
36
contusion: the brain banging against the opposite side
counter coup
37
most common demyelinating disease; plaques in white matter
multiple sclerosis
38
most common cause of dementia in the elderly; amyloid plaques and neurofibrillary tangles
alzheimer's disease
39
beta-amyloid protein
amyloid plaques
40
tau protein
neurofibrillary tangles
41
loss of pigmented neurons in substantia nigra; movement disorder; lewy bodies
parkinson's
42
involuntary writhing movements: chorea; depression and dementia; expansion of CAG triplet; atrophy of caudate nucleus and cortex
huntington disease
43
degeneration of upper and lower neurons; muscle atrophy and weakness spasticity; bunina bodies
amytrophic lateral sclerosis
44
very malignant; most common in kids; occurs in cerebellum; small round blue cells forming Homer Wright pseudorosettes
medulloblastoma
45
glial tumor: necrosis and pseudopallasading; ring enhancing lesion; microvascular proliferation
glioblastoma
46
glial tumor: commonly adulthood; cerebral hemispheres; "fried egg appearance", "satellitosis"
oligodendroglioma
47
glial tumor: mostly in ventricles or central canal of spinal cord; perivascular pseudorosettes
ependyomas
48
arise from cells covering brain and spinal cord; psammoma bodies
meningioma
49
most common tumor of the brain
metastatic tumor
50
inflammation limited to the meninges and the subarachnoid space; nuchal rigidity, photophobia and headache
meningitis
51
meningitis: usually bacterial; E coli, meningococcus
acute pyogenic meningitis
52
meningitis: viral; ECHO, coxsackie, EBV, HSV
acute lymphocytic meningitis
53
meningitis: prototype: M. tuberculosis
chronic meningitis
54
most due to bacteria from nasopharynx via bloodstream; congested meninges; exudate in subarachnoid space; brain tissue itself not infected
acute purulent meningitis
55
encephalitis: infection elsewhere travelling via bloodstream; adjacent infections in ear and sinuses
abscess
56
encephalitis: caseating granuloma
tuberculosis
57
encephalitis: typically AIDS patients, ring enhancing lesion
toxoplasmosis
58
encephalitis: most common cause of sporadic encephalitis in US; temporal lobes and orbital frontal areas
herpes simplex virus type 1
59
encephalitis: classi negri bodies in neurons; symptoms occur too late
rabies
60
associated with abnormal prion protein; Creutzfeldt Jakob Disease
transmissible spongiform encephalitis
61
highly resistant to heat and most disinfectants; abnormally folded forms cannot be cleared from the brain and cause toxicity
prion protein