NM Cranial And Peripheral Nerve Disorders Flashcards

1
Q

Wallerian Degeneration: transection (_____) results in degeneration of ____ and ___ ___ distal to site of ____ interruption

A

NEUROTMESIS
Axon and myelin sheath
Atonal

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2
Q

Segmental demyelination: Axons are ____ (no _____ degeneration); demyelination restores function (Ex: _____)

A

Preserved
Wallerian
GBS

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3
Q

Axonal degeneration: degeneration of ____ ____ and myelin, progressing from ___ to ___, “dying back” of nerves (ex: ______)

A

Axon cylinder
Distal to proximal
peripheral neuropathy

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4
Q

Chromatolysis and repair occur in ____

A

nerve cell body

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5
Q

______ (sheath) does not regenerate in Wallerian Degeneration, but forms tube directing regeneration

A

Endoneurium

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6
Q

Neuropathy

A

Any disease of nerves characterized by deterioration of neural function

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7
Q

Polyneuropathy: _____ _____ involvement of peripheral nerves, usually ____ > ____ (UE vs. LE), distal segments earlier and more involved than proximal

A

B/L symmetrical

UE>LE

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8
Q

Mononeuropathy

A

Involvement of single nerve

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9
Q

Involvement of nerve roots

A

Radiculopathy

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10
Q

3 types of traumatic nerve injury

A
  1. Neurapraxia (class 1)
  2. Axonotmesis (class 2)
  3. Neurotmesis (class 3)
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11
Q

Neurapraxia (class 1): injury to nerve that results in ___ loss of function (conduction block ischemia); nerve dysfunction may be rapidly ___ or persist few weeks (ex: ____)

A

Transient
Reversed
Compression

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12
Q

Axonotmesis (Class 2): injury to nerve interrupting ___ and causing loss of function and ___ ___ distal to lesion; with no disruption of ___, regeneration possible (ex: ____)

A

Axon
Wallerian degeneration
Endoneurum
Crush injury

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13
Q

Neurotmesis (class 3): cutting of nerve with ___ of all structure and complete loss of function; reinnervation typically fails without ___ ___ because of aberrant regeneration (failure of regenerating axon to find its ____ ____)

A

Severance
Surgical intervention
Terminal end

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14
Q

Autonomic dysfunction from LMN may present as

A

Vasodilation and loss of vasomotor tone (dryness, warm skin, edema, orthostatic hypotension)

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15
Q

Hyperexcitability of remaining nerve fibers following LMN syndrome: sensory dysthesias (___, pins/needles, numbness, ____). Motor responses include ___ and ___.

A

Hyperalgesia
Burning
Fasciculations and spasms

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16
Q

Myalgia

A

Muscle pain

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17
Q

EMG studies for motor nerve function: examine for signs of widespread denervation atrophy (___ ___ potentials); evidence of reinnervation appears as ____ amplitude, ____ duration, _____ motor unit potentials)

A

Spontaneous fibrillation
Low
Short
Polyphasic

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18
Q

Trigeminal neuralgia usually due to degeneration or compression- what is compressed?

A

Tortuous basilar A or cerebellopontine tumor

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19
Q

Mean age for trigeminal neuralgia? Gradual or abrupt onset?

A

> 50, abrupt onset

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20
Q

Characteristics of trigeminal neuralgia?

A

Brief paroxysms of neuralgic pain (stabbing/shooting); recurring frequently

21
Q

Trigeminal neuralgia autonomic instability exacerbated by ___ and ___, relieved by ____

A

Stress, cold

Relaxation

22
Q

Bell’s Palsy is lesion of CN ___

A

VII

23
Q

Bell’s palsy is compression of nerve within ___ bone

A

Temporal

24
Q

Lack of salivation and lacrimation, paralysis/weakness of muscles of facial expression on 1 side

A

Bell’s Palsy

25
Q

Testing for muscles of facial expression (Bell’s Palsy)- have pt:

A

Wrinkle forehead, raise eyebrows, frown, smile, close eyes tight, puff out cheeks

26
Q

Etiology of bulbar palsy

A

Tumors, vascular degeneration, diseases of lower CN motor nuclei

27
Q

Bulbar palsy refers to weakness or paralysis of muscles innervated by ____ ___ of lower brainstem, affecting muscles of face, ____, ___, ___.

A

Motor nuclei

Tongue, larynx, pharynx

28
Q

Examine ___ and ___ paralysis: phonation, articulation, palatial action, gag reflex, swallowing

A

Glossopharyngeal and vagal

29
Q

Possible complications of bulbar palsy

A

Aspiration pneumonia, severe airway restriction with dyspnea (B/L involvement), difficulty with coughing

30
Q

Pseudobulbar palsy: ____ (U/L or B/L) dysfunction of ______ innervation of brainstem nuclei; central or UMN lesion analogous to _____ lesions disrupting function of anterior horn cells

A

B/L
Corticobulbar
Corticospinal

31
Q

Pseudobulbar palsy: similar sx as bulbar palsy; examine for ____ reflexes, increased jaw jerk, ____ ____ (tapping lips results in pouting of lips)

A

Hyperactive

Snout reflex

32
Q

PT goals/outcomes for bulbar palsy (4)

A
  1. Suctioning/oral care
  2. Maintenance of respiratory function, open airway
  3. Elevate HOB
  4. Dietary changes: soft foods, liquids
33
Q

Acute ascending symmetrical polyneuropathy

A

GBS

34
Q

GBS is polyneuritis with ___ muscle weakness that develops ____. Etiology unknown but usually associated with _____ attack, after recovery from _____ _____ (respiratory or GI).

A

Progressing, rapidly
Autoimmune
Infectious illness

35
Q

GBS: Acute demyelination of both ___ and ___ (___ disease).

A

CN, peripheral nerves

LMN

36
Q

GBS: Sensory loss ___ (< or >) motor loss

A

Less than

37
Q

GBS: Motor paresis or paralysis shows relative ____ distribution of weakness. Progressive from ___ to ___ (UE/LE) , ____ to ____ (prox/distal). May produce _____ with ____ failure.

A

LE —> UE
distal —> proximal
Tetraplegia, respiratory

38
Q

GBS: progression evolves over few days or weeks, recovery slow (___ - ____), usually complete (85% of cases), some mild weakness may persist, 3% mortality

A

6 mo-2 yrs

39
Q

Complications with GBS (6)

A
  1. Respiratory impairment/failure
  2. Autonomic instability (tachycardia, arrhythmias, BP flux)
  3. Pain: myalgias
  4. Risk of pneumonia
  5. Prolonged hospitalization/immobility (contractures, DVT, skin)
  6. Relapse if tx inadequate
40
Q

CN to examine for GBS

A

VII, IX, X, XI, XII

41
Q

ALS: degenerative disease affecting ___ and ___. Degeneration of ____ ____ ____ and descending corticobulbar and ____ tracts.

A

UMN, LMN
Anterior horn cells
Corticospinal

42
Q

ALS: etiology unknown (____ or ____). ______% genetic (___ dominant).

A

Autoimmune or viral
5-10%
Autosomal

43
Q

ALS: progressive disease, often leading to death typically in ____ years. Highly variable symptoms: 2 onsets are?

A

2-5 yrs

  1. Bulbar onset: progressive bulbar palsy
  2. Spinal cord onset: progressive muscle atrophy
44
Q

Stages of ALS:

Stage I: early disease, mild focal ____, ____ distribution; symptoms of ____ cramping and fasciculations

A

Weakness
Asymmetrical
Hand

45
Q

Stages of ALS:

Stage II: ___ weakness in groups of muscles, some atrophy, ____ with ____ (assist level)

A

Moderate

Mod I with AD

46
Q

Stages of ALS

Stage III: ___ weakness of specific muscles, increased ____, mild to moderate functional limitations, ____

A

Severe
Fatigue
Ambulatory

47
Q

Stages of ALS

Stage IV: ___ weakness and ____ of LEs, ___ weakness of UEs. ______ and _____ required, _____ (assist levels)

A
Severe
Wasting
Mild
ModA and ADs
W/C user
48
Q

Stages of ALS
Stage V: _____ weakness with deterioration of mobility and _____, increased ____, moderate to severe weakness of _____ and ____; ____, ____ (UMN), loss of head control, ____ (assist level)

A
Progressive
Endurance
Fatigue
LEs and trunk
Spasticity, hyperreflexia
Total assist
49
Q

Stages of ALS

Stage VI: _____, dependent for ADLs/FMS, progressive ___ ___

A

Bedridden

Respiratory distress