NEURO Flashcards

1
Q

Subclavian steal syndrome:
presentation?
dx?
tx?

A

asx at rest, but arm claudication and CNS sx with exercise due to stenotic subclavian artery (can present like a TIA)

Dx arteriogram

Tx bypass surgery

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Presentation of:
Carotid TIA?
Vertebrobasilar TIA?

A

Carotid TIA: abrupt contralateral sx

Vertebrobasilar TIA: ipsilateral CN palsy, contralateral hemiplegia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Transient global amnesia:
location?
presentation?

A

TIA in temporal lobes or thalamus → rapid retrograde memory loss + confusion but preservation of self-identity

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Presentation of ACA syndrome:

A

contralateral leg hemiparesis, incontinence

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Presentation of MCA syndrome:

A

contralateral face/arm hemiparesis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Presentation of PCA syndrome:

A

homonymous hemianopia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Presentation of Cerebellar infarction:

A

headache, nausea, vomiting, vertigo, nystagmus

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Presentation of Lacunar syndromes:

tx?

A

pure motor or sensory stroke, clumsy hand-dysarthria syndrome

control htn

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

 Basal skull fx presentation?

A

raccoon eyes, hemotympanum, otorrhea, rhinorrhea, ecchymosis behind the ear (Battle sign)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Shy-Drager syndrome:

A

PD + autonomic insufficiency

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Progressive supranuclear palsy (PSP):

A

PD w/o ophthalmoplegia or tremors

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Creutzfeldt-Jakob disease:
presentation?
dx?

A

rapidly progressive dementia, myoclonus (muscle spasms), personality changes

EEG (generalized sharp waves) + postmortem

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Vital signs a/w incr ICP?

A

↑BP, ↓HR, irregular RR

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Bilateral vs Unilateral fixed/dilated pupil:

A

Bilateral fixed/dilated pupils: severe anoxia

Unilateral fixed/dilated pupil: herniation w/ CN III compression

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Pinpoint pupils =

A

ICH in pons vs narcotics

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

“Locked in” syndrome is caused by damage to…

A

ventral pons

17
Q
Result of brain herniation with compression of:
CNIII?
PCA?
crus cerebri?
brainstem causes?
A

CN III: ipsilateral “blown pupil”

PCA: contralateral homonymous hemianopia

Crus cerebri: ipsilateral paresis

Brainstem: Duret hemorrhages, death

18
Q

ddx for Ring-enhancing lesions:

A

metastases, abcesses, lymphoma, toxo

19
Q

MC brain cancers:

A

metastases (overall), astrocytoma (adults), infratentorial tumors (kids)

20
Q

“fried egg” cells, chicken-wire capillary pattern

A

Oligodendroglioma

21
Q

S-100+

A

Acoustic schwannoma

22
Q

Rosenthal fibers

A

Astrocytoma

23
Q

GFAP+

A

GBM + Astrocytoma

24
Q

Psamomma bodies

A

Meningioma

25
Q

pseudo- palisading necrosis

A

GBM

26
Q

Meningeal carcinomatosis:
presentation?
tx?

A

focal neuro sx, meningitis, hydrocephalus

intrathecal chemotherapy

**metastasizes to meninges via bloodstream

27
Q

Myasthenia gravis:
dx?
tx for myasthenic crisis?

A

↑anti-nAChR (best), edrophonium test, EMG (decreased response w/ repetitive stimulation), chest CT to look for thymoma

emergent ventilation

28
Q

Lambert-Eaton myasthenic syndrome (LEMS):
presentation?
dx?

A

gradually progressive muscle weakness that get better w/ repetitive muscle use

Dx ↑anti-VGCC (voltage gated Ca channel)

29
Q

Neurofibromatosis type I (von Recklinghausen disease):

presentation?

A

café-au-lait spots, Lisch nodules (iris hamartomas), CNS tumors, pheo

30
Q

Neurofibromatosis type II:

presentation?

A

bilateral acoustic neuromas, juvenile cataracts

31
Q

Tuberous sclerosis:

presentation?

A
  • CNS/retinal hamartomas
  • sebaceous adenomas
  • hypopigmented “ash leaf spots”
  • Shagreen patches
  • renal angiomyolipoma
  • cardiac rhabdomyoma
32
Q

Sturge-Weber syndrome:

presentation?

A

facial “port-wine stain” w/ ipsilateral brain AVM

33
Q

Von Hippel-Lindau disease:

presentation?

A

hemangioblastomas, bilateral RCC, pheochromocytomas