N3 Flashcards

(55 cards)

1
Q

deep lacunar stroke risk factors

A

hypertension, hyperlipidemia, and smoking

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2
Q

deep lacunar stroke occurs due to

A

occlusion of a single, deep penetrating artery in the brain

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3
Q

underlying pathology for deep lacunar stroke

A

combination of microatheroma (fat or fibrous deposition) and lipohyalinosis (segmental arteriolar disorganisation - thickening)

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4
Q

lacunar infarcts are usually of

A

thrombotic origin

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5
Q

lacunar infarct on non-contrast CT

A

not seen due to their small size

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6
Q

most common site for a lacunar infarct is

A

posterior limb of the internal capsule

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7
Q

posterior limb of the internal capsule infarct results in

A

a pure motor stroke

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8
Q

posterior limb of the internal capsule infarct results in a pure motor stroke by affecting

A

corticospinal and some corticobulbar motor fibers located in the genu

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9
Q

posterior limb of the internal capsule symptoms

A

affects the contralateral face, arm and leg equally

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10
Q

other common lacunar stroke infarcts

A

ataxic hemiparesis, clumsy hand dysarthria, pure sensory stroke and mixed sensory motor stroke

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11
Q

progressive signs and symptoms of elevated ICP =

A

headache, vision changes, nausea, vomiting and papilledema - brain tumor

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12
Q

progressive signs and symptoms of elevated ICP on CT

A

mass lesion, edema, or midline shift on non contrast CT

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13
Q

causes of embolic stroke

A

carotid artery thrombsis

cardiac emboli

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14
Q

what vessels do embolic strokes affect?

A

large vessels

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15
Q

lacunar infarcts are usually of what etiology

A

rarely embolic

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16
Q

cardiac emboli causing a stroke

A

mural thrombi in patients with chronic A Fib may send emboli to the CNS

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17
Q

cocaine and methamphetamines causing a stroke

A

drug induced vascular spasm - younger patient

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18
Q

unilateral throbbing pain, nausea, phonophobia, and photophobia

A

migraine headaches

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19
Q

headaches, altered sensorium and seizures

A

subarachnoid hemorrhages and subdural hematomas

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20
Q

NF1 diagnosis

A

von Recklinghausen disease

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21
Q

NF2 diagnosis

A

central neurofibromatosis

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22
Q

NF1 gene mutation

A

NF1 tumor suppressor gene: codes for the protein neurofibromin

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23
Q

NF2 gene mutation

A

NF2 tumor suppressor gene: codes the protein merlin

24
Q

NF1 gene location

A

chromosome 17

25
NF2 gene location
chromosome 22
26
NF 1 main clinical features
café au lait spots multiple neurofibromas lisch nodules
27
NF2 main clinical features
bilateral acoustic neuromas
28
NF1 inheritance pattern
autosomal dominant neurocutaneous syndrome
29
most common type of intracranial lesion for NF1
optic pathway glioma
30
most common type of intracranial lesion for NF1 manifests when
during toddlerhood
31
bilateral sensorineural hearing loss
bliateral acoustic neuromas = vestibular schwannomas
32
bilateral acoustic neuromas are diagnostic of
NF2
33
best initial screening test for the diagnosis of acoustic neuromas
audiometry
34
NF1 patients are at inc risk for
epilepsy - EEG is not indicated without seizures
35
lumbar punctures are performed in headaches to rule out
infections - meningitis, encephalitis
36
absence of fever and chronic nature of a headache would suggest
non infectious, growing intracrainial neoplasm
37
chronic headaches and blurry vision
adrenal adenoma can cause hyperaldosteronism and secondary hypertension
38
suspicion of adrenal adenoma
renin-aldosterone ratio is measured
39
neurocutaneous syndrome associated with intracrainial tumors
tuberous sclerosis
40
tuberous scleosis genes
TSC1 and TSC2
41
subependymal giant cell astrocytomas
tuberous sclerosis
42
subependymal nodules
tuberous sclerosis
43
cotical tubers
tuberous sclerosis
44
additional characteristics of tuberous sclerosis
``` hypopigmented macules (ash leaf spots) facial angiofibromas cardiac rhabdomyomas renal angioleiomyomas mental retardation seizures ```
45
a young boy with symptoms of inc intracranial pressure, bitemoral hemianopsia and a calcified lesion above the sella has
craniopharyngioma
46
craniopharyngioma is characterized by
nests of squamous cells in a loose stroma, resembling the appearance of embryonic tooth bud enamel
47
location of craniopharyngioma
suprasellar and inf to optic chiasm
48
craniopharyngioma endocrine symptoms
diabetes insipidus | growth failure - hypothyroidism or GH def
49
presence of a cystic calcified parasellar lesion on MRI
almost diagnostic of craniopharyngioma
50
pituitary adenoma vs craniopharyngioma
pituitary adenoma is more common in women | prolactinoma is an important part of this syndrome
51
non-invasive tumors derived from arachnoid cap cells
meningiomas
52
meningiomas consist of
concentric whorls and calcified psammoma bodies
53
meningiomas - location and consequence thereof
it may indent the brain and cause hyperostosis and usually occur on the convex surfaces of the brain
54
enlarged sella turcica with no pituitary gland due to
empty sella syndrome due to an incompetent sellar diaphtragm with compression of the pit gland by the herniating arachnoid or secondary to surgery radiotherapy
55
ependymoma
gliomas and are benign