anatomy Flashcards

1
Q

T1W brain MRI

A

CSF dark
white matter white
grey matter grey
gandolinium BRIGHT

good view of anatomy

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2
Q

T2W

A

CSF bright
inflammation or injury bright
white and grey matter SWAPPED

good to look at inflammation and injury, but not the best since CSF is also bright

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3
Q

T2W Flair

A

T2W but CSF is blacked out making it SUPER easy to see pathology (strokes, inflammation, white matter disease) - this is the go to!

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4
Q

DWI

A

STROKE view, will be BRIGHT; pair with ADC image, will make acute stroke lesion dark - if bright in both then it is a chronic process

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5
Q

T2 series

A

microhemorrhages

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6
Q

dural sinus thrombosis

A

essentially DVT surrounding the brain; evaluate with venography

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7
Q

CTA

A

arteries of head and neck

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8
Q

limitation of CTA

A

pt with poor renal function GFR < 30

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9
Q

how long for ischemic stroke to be visualized in CT

A

up to 6 hrs; best used to evaluate hemorrhagic

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10
Q

subdural hemorrhage

bridging veins

A

old patient

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11
Q

epidural hemorrhage
middle meningeal artery
risk of herniation
surgical drainage

A

skull fracture/trauma

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12
Q

what makes an enhanced CT?

A

Is there contrast in the blood vessels?

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13
Q

Which structure on MRI can you look to determine type?

A

Corpus collosum - should be white; cortex should be grey

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14
Q

achilles reflex

A

S1 + tibial

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15
Q

patellar reflex

A

L2,3,4 + femoral

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16
Q

brachioradialis reflex

A

C5,6

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17
Q

biceps reflex

A

C 5,6 + musculocutaneous

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18
Q

triceps reflex

A

C 6,7

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19
Q

finger jerk

A

C8

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20
Q

pectoral reflex

A

C5

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21
Q

medial hamstring reflex

A

L5

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22
Q

carpal tunnel syndrome is impingement of this nerve

A

median

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23
Q

shoulder abduction

A

C5 + axillary

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24
Q

elbow flexion

A

C5,6 + musculocutaneous

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25
Q

elbow extension

A

C6,7 + triceps

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26
Q

wrist extension

A

C6,7 + radial

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27
Q

finger extension

A

C7,8 + radial

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28
Q

wrist flexor/pronato

A

C6,7 + medial/ulnar

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29
Q

distal thumb flexors

A

C8 + median

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30
Q

finger abduction

A

C8,T1 + ulnar

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31
Q

hip flexion

A

L1,2 + femoral

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32
Q

hip abduction

A

L5 + superior gluteal

33
Q

hip adduction

A

L2,3,4 + obturator

34
Q

knee extension

A

L2,3,4 + femoral

35
Q

knee flexion

A

L5, S1 + sciatic

36
Q

ankle dorsiflexion

A

L4,5 + deep fibular

37
Q

plantar flexion

A

S1,2 + tibial

38
Q

toe extension

A

L5 + deep fibular

39
Q

ankle inversion

A

L5 + tibial

40
Q

NMJ disease, automimmune, CXR to evaluate thymus, attack of ACh receptor, fatigable weakness - diplopia and ptosis, scary risk of breathing issues, worsened by many abx

A

Myasthenia Gravis

41
Q

dysfunctional peripheral nerve myelin; weakness, atrophy and sensory loss; foot deformity

A

CMT; type 1A is common AD type w/ loss of intrinsic hand and foot muscles

42
Q

sporadic myopathy, weakness, elevated CK, muscle tenderness and atrophy, dx with muscle biopsy and EMG

A

inclusion body myositis (if rash, would need to rule out dermatomyositis)

43
Q

immune mediated inflammation, peripheral nerve myelin of spinal nerve roots, recent GI or respiratory infx, ascending weakness, tx with IVIG and plasma exchange, CSF with cytoalbuminologic dissociation, EMG/NCS 2wks following

A

Guillan Barre

44
Q

fatigue, focal onset weakness, muscle wasting, brisk reflexes, fasiculations that progress over time; UMN and LMN, EMG/NCS critical to dx, Riluzole to delay symptoms + symptom mgmt

A

ALS

45
Q

progressive muscle weakness, X-linked genetic conditions, dysfunction in muscle protein leading to breakdown and replacement by fatty tissue, elevated CK, cardiomyopathy, prednisone delays progression

A

muscular dystrophy; Duchenne develops YOUNG, whereas Becker can present later and progress slower

46
Q

initial labs for peripheral neuropathy

A

B12, A1C, Thyroid function, serum electrophoresis + immunofixation, ESR

47
Q

causes to consider if rapid onset of neuropathy, 1 month or less

A

toxin/drug, GBS, infection, vasculitis, prophyria

48
Q

rx to lessen neuropathy

A

tricyclics (amitryptaline), venlafaxine/duloxetine, gabapentin/pregabalin, topical lidocaine/capsaicin, carbamazepime

49
Q

pernicious anemia and nitrous oxide are common causes of _____ deficiency

A

B12

50
Q

B12 deficiency leads to high levels of ____

A

Methylmalonic acid (MMA) - toxic to nerves

51
Q

low B12/high MMA causes

A

peripheral neuropathy + degeneration of dorsal colums ( ataxia, proprioceptive loss) + corticospinal tract degeneration ( weakness)

52
Q

corticospinal tract

A

motor

53
Q

ventral horn

A

motor tracts

54
Q

sudden onset right hemiplegia and aphasia

A

left cerebral hemspheric infarction

55
Q

papilledema and subacute onset amenhorrhea and bitemporal hemianopia

A

pituitary tumor

56
Q

weakness of right abductor pollicis brevis and numbers of the first 3 1/2 digits of hand

A

median neuropathy/CTS

57
Q

progressive diffuse weakness, atrophy, fasciulation, spasticity + loss of anterior horn cells and degeneration of corticospinal tracts

A

ALS

58
Q

progressive loss of virbation and propriocipeton in B12 deficiency is due to syfunction in

A

posterior colum

59
Q

delirium, mydriasis, hypertension, dry mouth, urinary retention, constipation

A

atropine overdose, blockade of muscarinic cholinergic receptors

60
Q

these sx are due to damage where?

CN deficits, imparied LOC, crossed or bilateral mortor or sensory deficits

A

brainstem

61
Q

lesion here would cause ataxia, tremor, nystagmus

A

cerebellum

62
Q

lesion here would cause LOC or memory disturbances, hemisensory loss and/or pain, hemiataxia, neglect or aphasia

A

thalamus

63
Q

lesion here would cause chorea, athetosis, dystonia, tremor, rigidity

A

basal ganglia

64
Q

symptmos of enecephalopathy (cerebral cortex)

A

hemilgeia and/or hemisensory loss, apphasia, neglect, hemianpia, dementia, seziure

65
Q

if patient has apahasia, where can you locate the lesion

A

dominant hemisphere (left for 95% of people)

66
Q

where is fascial nerve nucleus located

A

pons

67
Q

if patient has upper and lower fascial weakness, where could lesion sbe

A

pontinue or peripheral nerve

68
Q

these two CN pass through cerebelloponinte anlge which could be compromised by a tumor

A

VII and VIII

69
Q

weakness, twitching and cramping are the most common symptoms of this motor neuron disease

A

ALS

70
Q

motor neuron diseases that affect LMN older

A

spinal muscular atrophy, spinobulbar muscular atrophy, viral (polio, HIV, westnile), rare paraneoplastic syndromes

71
Q

motor neuron disease affecting mixed LMN and UMN

A

ALS

72
Q

motor neuron disease that affects UMN only

A

primary lateral sclerosis

73
Q

ALS Crorf72 can also have

A

frontotemporal dementia

74
Q

difficulty swallowing due to neuromuscular etiology likely to present as difficulty swallowing _____

A

liquids

75
Q

if mechanical cause of swallowing, will have difficulty with ____

A

solids

76
Q

dementia associated with ALS

A

frontotemporal dementia

77
Q

3 sites of pathology in ALSO

A

loss of anterior horn cells, degeneration of corticospinal tract, loss of betz cells in the cortex

78
Q

OTC migraine sx tx

A

naproxen, excedrin, advil

79
Q

DHE is what type of abortive migraine tx

A

ergotamine