Pestana11 Neuro Flashcards

(52 cards)

1
Q

Transient ischemic attack (HA +/-)

A

Without headache

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2
Q

TIA (workup, mgmt)

A
  • Duplex studies (sono+Doppler)

- CEA, Angioplasty+stent (need filter first)

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3
Q

TIA (mc etiology)

A
  • High grade stenosis (>70%) of internal carotid

- Ulcerated plaque at the carotid bifurcation

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4
Q

TIA (clinical significance)

A

Predictors of stroke

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5
Q

TIA vs Ischemic stroke (onset, sequela)

A
  • Suddent for both

- No sequela w/ TIA, permanent sequela w/ stroke

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6
Q

Ischemic stroke (complication)

A

Hemorrhagic stroke

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7
Q

Ischemic stroke (initial step)

A

CT scan to r/o extensive infarcts or presence of hemorrhage

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8
Q

Ischemic stroke (mgmt)

A
  • tPA w/in 4hr

- Rehabilitation

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9
Q

Ischemic stroke (workup after initial evaluation)

A

Vascular workup to identify lesions that may cause recurrence

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10
Q

Hemorrhagic stroke (dem, presentation)

A
  • Uncontrolled hypertensives

- Very severe HA of sudden onset

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11
Q

Hemorrhagic stroke (dx, mgmt)

A
  • CT scan
  • Control HTN
  • Rehabilitation
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12
Q

Subarachnoid hemorrhage (presentation)

A
  • Worst HA of sudden onset
  • May not have any neurological deficits (in subarachnoid space, ergo no mass effect); may have signs of meningeal irritation
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13
Q

Subarachnoid hemorrhage (etiology)

A

Ruptured aneurysm in the Circle of Willis

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14
Q

Subarachnoid hemorrhage (dx, mgmt)

A
  • CT scan (also bloody spinal tap, but not first line) followed by arteriogram to locate the aneurysm
  • Clipping (surgical)
  • Endovascular coiling (radiological alternative)
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15
Q

Brain tumors (presentation)

A
  • HA (worse in morning, progressive over mos)

- ICP (blurred vision, papilledema, projectile vomiting; Cushing reflex: bradycardia+HTN)

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16
Q

Brain tumors (dx)

A

MRI

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17
Q

Brain tumors (sxs mgmt)

A

High-dose steroids (dexamethasone: Decadron)

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18
Q

Tumors at the base of the frontal lobe (presentation 4)

A

Foster-Kennedy syndrome:

  • Inappropriate behavior
  • Ipsilateral optic nerve atrophy
  • Contralateral papilledema
  • Anosmia
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19
Q

Craniopharyngioma (features 3)

A
  • Short stature
  • Bitemporal hemianopsia
  • Calcified lesions above sella (xray)
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20
Q

Prolactinomas (presentation)

A

Amenorrhea and galactorrhea in young woman

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21
Q

Prolactinoma (work up 4)

A
  • Pregnancy test (r/o pregnancy)
  • TSH (r/o hypothyroidism)
  • Serum PRL
  • MRI of sella
22
Q

Prolactinoma (mgmt)

A
  • Bromocriptine (or analog)

- Transnasal, trans-sphenoidal removal (fertility; resistance to bromocriptine)

23
Q

Acromegaly (clinical features)

A
  • Huge hands, feet, tongue and jaw

- HTN, DM, sweaty hands, HA, rings/hats no longer fit

24
Q

Acromegaly (workup)

A
  • Somatomedin C (IGF-1) levels

- MRI of pituitary

25
Acromegaly (tx)
- Surgical removal | - Radiation (alternative)
26
Pituitary apoplexy (definition)
Bleeding into a pituitary tumor
27
Pituitary apoplexy (phases)
- Indolent phase | - Acute phase
28
Pituitary apoplexy (indolent phase sxs 3)
Pituitary tumor sxs: - HA - Vision loss - Endocrine problems
29
Pituitary apoplexy (acute phase sxs 3)
- Severe HA - Compression of nearby strxs (deterioration of remaining vision, b/l optic nerve pallor) - Destruction of pituitary (stupor, hypotension)
30
Pituitary apoplexy (dx)
CT/MRI
31
Pituitary apoplexy (initial mgmt)
-Steroid and hormone replacement
32
Tumors of the pineal gland (features 2)
- Loss of upper gaze | - "Sunset eyes" (Perinaud syndrome)
33
Brain tumors in children (location)
Posterior fossa
34
Brain tumors in children (sxs)
- Cerebellar sxs | - Children often assume knee-chest position to relieve HA
35
Brain abscess vs brain tumor
- Similar manifestation d/t space-occupation | - Abscess has a shorter timetable (1-2wks)
36
Brain abscess (features)
- Fever (not always) | - Obvious source of infection (eg, otitis media, mastoiditis, dental caries)
37
Brain abscess (dx)
CT w/ contrast
38
Tumors affecting the spinal cord (origin)
Metastatic/extradural
39
Tumors affecting the spinal cord (dx)
MRI
40
Tumors affecting the spinal cord (tx)
Decompression
41
Neurogenic claudication (clinical features)
- Exacerbated by walking - Relieved by rest - But both are position-dependent (hip flexion relieves; extension exacerbates)
42
Neurogenic claudication (etiology)
Spinal stenosis
43
Neurogenic claudication (dx)
MRI
44
Neurogenic claudication (mgmt)
Block affected nerves
45
Trigeminal neuralgia, aka tic douloureux (presentation)
Extremely severe, sharp, shooting pain in face triggered by touch (60s)
46
Trigeminal neuralgia, aka tic douloureux (workup)
MRI to r/o organic lesions
47
Trigeminal neuralgia, aka tic douloureux (mgmt)
- Anticonvulsants (first line) | - Radiofrequency ablation
48
Reflex sympathetic dystrophy, aka causalgia (onset)
Several months after crushing injury
49
Reflex sympathetic dystrophy, aka causalgia (features)
- Constant, burning, agonizing pain refractive to usual analgesics - Slightest stimulation aggravates pain
50
Reflex sympathetic dystrophy, aka causalgia (extremity appearance)
- Cold - Cyanotic - Moist
51
Reflex sympathetic dystrophy, aka causalgia (dx)
Sympathetic block
52
Reflex sympathetic dystrophy, aka causalgia (tx)
Sympathectomy