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 ___

23
Q

Bell’s palsy is compression of nerve within ___ bone

24
Q

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

A

Bell’s Palsy

25
Testing for muscles of facial expression (Bell’s Palsy)- have pt:
Wrinkle forehead, raise eyebrows, frown, smile, close eyes tight, puff out cheeks
26
Etiology of bulbar palsy
Tumors, vascular degeneration, diseases of lower CN motor nuclei
27
Bulbar palsy refers to weakness or paralysis of muscles innervated by ____ ___ of lower brainstem, affecting muscles of face, ____, ___, ___.
Motor nuclei | Tongue, larynx, pharynx
28
Examine ___ and ___ paralysis: phonation, articulation, palatial action, gag reflex, swallowing
Glossopharyngeal and vagal
29
Possible complications of bulbar palsy
Aspiration pneumonia, severe airway restriction with dyspnea (B/L involvement), difficulty with coughing
30
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
B/L Corticobulbar Corticospinal
31
Pseudobulbar palsy: similar sx as bulbar palsy; examine for ____ reflexes, increased jaw jerk, ____ ____ (tapping lips results in pouting of lips)
Hyperactive | Snout reflex
32
PT goals/outcomes for bulbar palsy (4)
1. Suctioning/oral care 2. Maintenance of respiratory function, open airway 3. Elevate HOB 4. Dietary changes: soft foods, liquids
33
Acute ascending symmetrical polyneuropathy
GBS
34
GBS is polyneuritis with ___ muscle weakness that develops ____. Etiology unknown but usually associated with _____ attack, after recovery from _____ _____ (respiratory or GI).
Progressing, rapidly Autoimmune Infectious illness
35
GBS: Acute demyelination of both ___ and ___ (___ disease).
CN, peripheral nerves | LMN
36
GBS: Sensory loss ___ (< or >) motor loss
Less than
37
GBS: Motor paresis or paralysis shows relative ____ distribution of weakness. Progressive from ___ to ___ (UE/LE) , ____ to ____ (prox/distal). May produce _____ with ____ failure.
LE —> UE distal —> proximal Tetraplegia, respiratory
38
GBS: progression evolves over few days or weeks, recovery slow (___ - ____), usually complete (85% of cases), some mild weakness may persist, 3% mortality
6 mo-2 yrs
39
Complications with GBS (6)
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
CN to examine for GBS
VII, IX, X, XI, XII
41
ALS: degenerative disease affecting ___ and ___. Degeneration of ____ ____ ____ and descending corticobulbar and ____ tracts.
UMN, LMN Anterior horn cells Corticospinal
42
ALS: etiology unknown (____ or ____). ______% genetic (___ dominant).
Autoimmune or viral 5-10% Autosomal
43
ALS: progressive disease, often leading to death typically in ____ years. Highly variable symptoms: 2 onsets are?
2-5 yrs 1. Bulbar onset: progressive bulbar palsy 2. Spinal cord onset: progressive muscle atrophy
44
Stages of ALS: | Stage I: early disease, mild focal ____, ____ distribution; symptoms of ____ cramping and fasciculations
Weakness Asymmetrical Hand
45
Stages of ALS: | Stage II: ___ weakness in groups of muscles, some atrophy, ____ with ____ (assist level)
Moderate | Mod I with AD
46
Stages of ALS | Stage III: ___ weakness of specific muscles, increased ____, mild to moderate functional limitations, ____
Severe Fatigue Ambulatory
47
Stages of ALS | Stage IV: ___ weakness and ____ of LEs, ___ weakness of UEs. ______ and _____ required, _____ (assist levels)
``` Severe Wasting Mild ModA and ADs W/C user ```
48
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)
``` Progressive Endurance Fatigue LEs and trunk Spasticity, hyperreflexia Total assist ```
49
Stages of ALS | Stage VI: _____, dependent for ADLs/FMS, progressive ___ ___
Bedridden | Respiratory distress