FA - Neuro Chapter Flashcards

1
Q

Riluzole

A

Think treatment for ALS b/c decreased presynaptic glutamate release.

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2
Q

Tabes dorsalis affects what 2 spinal areas.

A

1) Degeneration of posterior column (p/w: impaired sensation, proprioception)
2) Demyelination of dorsal nerve roots (p/w: progressive sensory ataxia so inability to sense or feel the legs)
3) Together lead to poor coordination, + Romberg, absent DTRs

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3
Q

Workup for Bell palsy.

A

Typically history and PE is enough to establish diagnosis but if paralysis lasts over 6-8 wks then explore other conditions like: AIDS, Lyme Disease, Sarcoidosis, Tumors or Diabetes

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4
Q

Other causes of stroke that should also be worked up for in addition to cardioemobolic and thrombotic causes.

A

Hypercoaguable state
Sickle cell disease
Vasculitis

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5
Q

Clinical features of MCA stroke.

A

Contralateral paresis and sensory loss in face and arm
Hemiparesis
Aphasia (dominant)
Neglect (non-dominant)
Gaze preference toward the side of the lesion

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6
Q

Biceps are innervated by what nerve root.

A

C5 nerve root

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7
Q

Triceps are innervated by what nerve root.

A

C7 nerve root

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8
Q

Patella innervated by what nerve root.

A

L4 nerve root

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9
Q

Achilles innervated by what nerve root.

A

S1 nerve root

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10
Q

Nerve roots responsible for Achilles reflex.

A

S1-2, tie your shoes

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11
Q

Nerve roots responsible for patellar reflex.

A

L3-4, kick the door

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12
Q

Nerve roots responsible for biceps reflex.

A

C5-C6, pick up sticks.

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13
Q

Nerve roots responsible for triceps reflex.

A

C7-8, lay them straight.

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14
Q

What BP is the limit for tPA administration.

A

SBP

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15
Q

Common symptoms of ACA stroke.

A

Contralateral paresis and sensory loss of LEG

Cognitive or personality change

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16
Q

PCA strokes distal to P-Comm affects what regions of the brain

A

Cortical temporal, occipital p/w P2 syndromes.

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17
Q

Types of Lacunar infarcts.

A

1) Pure motor [lesion in posterior limb of internal capsule containing corticospinal tract]
2) Pure sensory [lesion in Thalamic VPL nucleus p/w contralateral hemianesthesia/parathesia OR can also p/w Dejerine-Roussy syndrome = Thalamic pain syndrome (allodynia) seen after several weeks following a pure sensory thalamic stroke]
3) Ataxia hemiparesis [lesions in Internal capsule anterior limb, where injury to frontopontocerebellar tract causes Ataxia while injury to corticospinal tract causes hemiparesis]
4) Dysarthria/ clumsy hand [Anterior pons or basis pontis lesion]
5) Mixed [lesions in thalamus and internal capsule]

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18
Q

PCA stroke proximal to P-Comm affects what regions of the brain.

A

Midbrain, subthalamic nucleus, thalamus p/w P1 syndromes.

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19
Q

P1 syndromes are associated with proximal PCA strokes and include:

A

Midbrain strokes p/w:

1) ipsilateral oculomotor nerve [CN3] palsy [droopy eyelid + Down/Out + fixed pupil]
2) Injury to superior cerebellar peduncle [ataxia]
3) Injury to cerebral peduncle [contralateral hemiparesis]

Subthalamic nucleus injury p/w: Hemibalismus

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20
Q

Midbrain stroke p/w CN III palsy with contralateral ataxia is called.

A

Claude’s syndrome

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21
Q

Midbrain stroke p/w CN III palsy with contralateral hemiplegia is called.

A

Weber’s syndrome (Superior alternating hemiplegia), can also present with contralateral parkinsonism (substantia nigra)

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22
Q

P2 syndromes are associated with distal PCA strokes and include:

A

1) Contralateral homonymous hemianopsia with macula sparing

2) Bilateral: cortical blindness (blind with intact pupillary reflex). Can be unaware (Anton’s)

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23
Q

Dejerine-Roussy syndrome

A

Thalamic pain syndrome seen after several weeks of having a pure sensory thalamic stroke p/w: burning pain over the affected area exacerbated by light touch (allodynia)

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24
Q

Occlusion of the anterior spinal artery causes what syndrome? Features include:

A

Medial medullary syndrome:

1) injury to medial pyramid t/f corticospinal fibers affected [p/w: Contralateral hemiparesis 2/2 injury before it decussates in the low medulla/cord]
2) injury to medial lemniscus t/f dorsal column fibers affected [p/w: Contralateral ataxia, loss of tactile vibration/position sense]
3) injury to Hypoglossal nucleus, CN XII t/f ipsilateral tongue weakness [p/w: tongue deviation to side of the lesion]

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25
Q

Medial Pontine Syndrome.

A

1) Injury to corticospinal fibers p/w: Contralateral spastic hemiparesis [injury before decussates in low medulla/cord]
2) Injury to Medial lemiscus p/w: Contralateral ataxia, loss of tactile/position sense from injury to posterior column pathway
3) Injury to CN 6 or Abducens nerve p/w: Strabismus or ipsilateral lateral rectus muscle paralysis

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26
Q

Conditions associated with berry aneurysms.

A
Marfan syndrome
Aortic coarctation 
Kidney disease (AD, polycystic) 
Ehlers-Danlos syndrome 
Sickle cell anemia
Smoking
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27
Q

Early management of SAH:

A

1) Reduce bleeding via control of SBP (

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28
Q

Late management of SAH:

A

1) Seizure prophylaxis w/ Phenytoin, Valproic acid, Levetiracetam
2) Manage ICP w/ reverse Trendelenberg, Mannitol (hypertonic solution), Hyperventilation or craniotomy
3) Vasospam prevention [to prevent ischemic episodes] w/ CCB like Nimodipine and leaving BP ELEVATED to maintain CPP [= BP-ICP]

29
Q

Abortive tx for migraines.

A

Sumatriptans.

30
Q

Prophylaxis tx for frequent migraines.

A

Anticonvulsants like gabapentin, topiramate.
TCA like amitriptyline.
Beta-blockers like propanolol.
CCBs.

31
Q

Young woman with >30 BMI, p/w n/v/HA/tinnitus and papilledema think.

A

Idiopathic intracranial HTN or pseudotumor cerebri 2/2 obesity, tetracylines, growth hormone, excess Vit A but to treat FIRST start out with weight loss! Then acetazolamide, topiramate or if really bad serial LPs or shunt.

32
Q

Tx for cluster HA.

A

High flow O2

33
Q

Onset of HA after the age of 50 in a woman but rule out.

A

Temporal arteritis, via obtaining an ESR

34
Q

First line anticonvulsant in children with partial or tonic-clonic (grand mal) seizures.

A

Phenobarbital.

35
Q

First line anticonvulsant in children with absence seizures (petit mal).

A

Ethosuximide.

36
Q

Acute vestibular neuritis

A

P/w vertigo + vomiting/nystagmus 1 wk after a viral infection w/o auditory sxs.

37
Q

Labyrinthitis.

A

P/w tinnitis, ear fullness, or hearing loss, + severe vertigo with n/v/nystagmus.

38
Q

Meniere disease.

A

Vertigo + Tinnitis + Hearing loss + EAR FULLNESS

39
Q

Pt experiences nausea, warmth and diaphoresis prior to what type of syncope.

A

Vasovagal syncope.

40
Q

Autonomic neuropathy associated with which type of syncope.

A

Orthostatic hypotension syncope.

41
Q

Myasthenic crisis

A

IVIG or plasmapheresis.

42
Q

Tx Meniere disease.

A

Acute: Meclizine
Chronic: Diuretics and low SALT diet

43
Q

Tx of Labyrinthitis/Vestibular Neuritis.

A

If within 72 hrs, steroids.

If after 72 hrs, meclizine for vertigo episodes.

44
Q

What is spared in Lambert-Eaton syndrome (that is not spared in MG)?

A

1- Extraocular muscles
2- Respiratory muscles
3- Bulbar muscles (hence why MG pts can have dysarthria, dysphagia)

45
Q

Charcot’s Triad.

A

Seen in MS:

1) Scanning speech
2) Internuclear opthalmoplegia
3) Nystagmus

46
Q

Multiple Sclerosis MRI.

A

Multiple, asymmetric, often periventricular white matter lesions (Dawson fingers), especially in the corpus callosum. Active lesion enhance with gadolinium.

47
Q

Multiple Sclerosis CSF.

A

Increase IgG index or at least 2 oligoclonal bands.

48
Q

Acute MS exascerbations.

A

IV steroids or plasma exchange if do not respond to corticosteroids.

49
Q

Long term tx of MS.

A

Immune-modulating agents: Interferon Beta 1-a/1-b, Copaxone. (ABCs)

50
Q

Presentation of Guillain-Barre.

A

Ascening paralysis
Areflexia
Paresthesias (2/2 sensory nerve demyelination)
Autonomic dysregulation (2/2 autonomic nerve demyelination)

51
Q

Dx of Guillain-Barre.

A

Nerve conduction studies.

52
Q

Guillian-Barre CSF.

A

High CSF protein > 55, albuminocytologic dissociation.

53
Q

What is spared in Amyotrophic Lateral sclerosis?

A

Sensation
Extraocular movements (high cranial nerves)
Sphincter tone

54
Q

Pick bodies

A

Round intraneuronal inclusions, tau

55
Q

Lewy bodies

A

Clumps of alpha-synuclein proteins

56
Q

Features of normal aging with regards to memory.

A

Patients can perform ADLs, complain of their memory loss yet provide detailed information about their forgetfulness, MMSE score >24.

57
Q

Gait associated with NPH.

A

Magnetic gait with feet “glued” to the floor.

58
Q

Type of myoclonus associated with CJD.

A

Startle-induced myoclonus.

59
Q

Bilateral tremors in person with family history of tremors.

A

Think Essential Tremor.

60
Q

Tx for essential tremor.

A

Propanolol or primidone (anticonvulsant of barbiturate class).

61
Q

Chromosome 9

A

Friederich ataxia

62
Q

Chromosome 4

A

Huntington disease

63
Q

Reserpine or tetrabenazine.

A

Huntington disease , used to reduced release of DA vesicles.

64
Q

Festinating gait.

A

Small, shuffling steps seen in Parksinson’s patients along with ABSENCE of arm swing.

65
Q

Tx for early/temporary Parksinsonian activity.

A

Amantadine.

66
Q

Side effects of Amantadine.

A

Ankle edema, ataxia, livedo reticularis.

67
Q

Side effects of Levodopa/carbidopa.

A

Nausea, vomiting, hallucinations, agitation.

68
Q

Side effects of Dopamine agonists.

A

Confusion, hallucinations, compulsive gambling

69
Q

Tx of tremor dominant Parkinson.

A

Anticholinergics (trihexyphenidyl or benztropine)