39 Radiculopathy, Neuropathy Flashcards

1
Q

Roots that do not contain sensory nerve fibers
?

A

C1, Co1

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2
Q

Cervical herniations MC affect:

A

C7&raquo_space; C6

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3
Q

Cervical spondylosis MC affects:

A

C5, C6

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4
Q

Cervical spondylosis:

Epidemiology?

A

60+ y/o, M>F (slight)

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5
Q

Lumbosacral radiculopathies MC affect:

A

L5, S1

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6
Q

Signs/symptoms associated with radiculopathies?

A
  1. sharp, electric, radiating pain; worsened by movements that stretch the nerve root
  2. Weakness/Atrophy: motor nerve fibers w/in myotome lost (1 root affected = one myotome lost)
  3. Paresthesias (sensory nerve fibers for dermatome are lost)
  4. Muscle Stretch Reflexes: ↓ ~ classic LMN disease finding
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7
Q

Cervical Maneuvers associated with cervical radiculopathy?

A

neck extension (best), neck rotation, Spurling’s Maneuver

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8
Q

Epidemiology of disc herniations?

Epidemiology of spondylosis?

A

50 yo

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9
Q

MC cause of cervical spondylosis?

A

myeloradiculopathy (Spinal Canal Stenosis)

**can present ~ALS from compression of CST

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10
Q

MC causes of lumbosacral spondylosis?

A
  1. neurogenic claudication (ambulation –> lower extremity pain/weakness)
  2. Cauda Equina Syndrome
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11
Q

What bone conditions/injuries contribute to radiculopathy? How?

A
  1. Trauma (younger patients ): causes spinal column instability = ↑risk of radiculopathy
  2. Bone Disease:
    - osteoporosis/malacia
    - Paget’s Disease
    - AVN from pro-longed steroids (SLE)
  3. Neoplastic
    - constitutional symptoms (weight loss)
    - Cauda Equina Syndrome
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12
Q

Imaging for dx of radiculopathy?

A

MRI

greater contrast sensitivity + Gadolinium Contrast allows det scar tissue vs. disk protrusion

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13
Q

Function of EDX?

A

confirms clinical diagnosis from History and Physical

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14
Q

EDX assesses:

A
  • sensory/motor nerves
  • muscle fibers
  • demyelination + axon loss
  • location of d/o
  • severity/prognosis
  • diagnosis
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15
Q

Conservative trx for radiculopathy?

A
  • *most improve w/in 6 weeks
  • AVOID Bed Rest: be as routine as possible
  • PT
  • Rx: pain, steroids, nerve blockers
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16
Q

Features of polyneuropathy?

A

symmetric/distal weakness in glove/stocking pattern

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17
Q

Features of Mononeuritis?

A

weakness + sensory loss in nerve’s distribution pattern (myotome/dermatome)

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18
Q

Features of Mononeuritis complex?

A

multiple myotomes/dermatomes involved

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19
Q

Findings of plexopathies (LMN Disease)?

A
  • ↓reflex
  • ↓conduction velocity
  • denervation/↓# motor units on EMG
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20
Q

Muscle biopsy in plexopathies (LMN Disease)?

A

atrophic fibers + fiber type grouping

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21
Q

Lesion of Median nerve?

A

Carpal Tunnel = numbness in Lateral 3.5 Digits + Atrophy of Thenar Compartment
(weakness in wrist flexion)

22
Q

Lesion of Ulnar nerve?

A

medial elbow entrapment =

  • Numbness in 5th and 1/2 of 4th Digits
  • Atrophy of Hypothenar/Interosseous
23
Q

Lesion of radial nerve?

A

axillary entrapment = wrist drop

24
Q

Lesion of peroneal nerve?

A

compr at fibular head or knee = foot drop

25
Demyelinating Neuropathy: | Nerves Affected?
large myelinated axons = - fibers joining muscles - fibers for reflexes - position/vibratory sense
26
Demyelinating Neuropathy: | Path?
patchy segmental demyelination with preservation of axon
27
Demyelinating Neuropathy: | Symptoms?
weakness (proximal + distal), ↓reflexes, ↓epicritic + intact protopathic
28
Demyelinating Neuropathy: | Diseases?
Guillain Barre, Diphtheria, Diabetes
29
Axonal Neuropathy: | Etiology?
Uremia + Toxins
30
Axonal Neuropathy: | Symptoms?
- distal areflexia - stocking-glove sensory deficit - trophic changes
31
Axonal Neuropathy: | Pathology?
myelin ovoids characteristic of axonal degradation
32
Axonal Neuropathy: | Nerve conduction?
normal w/↓amplitude of APs
33
Wallerian Neuropathy: | Etiiology?
trauma + Vasculitis
34
Wallerian Neuropathy: | Path?
Toluidine blue stain demonstrates pale fascicle area without myelinated fibers
35
Charcot Marie Tooth Disease: | Etiology?
hereditary (AD) disease, periph demyelinating: - Type 1A: del of myelin protein PMP Ch. 17 - Type 1B: def of protein 0 Ch. 1 **PMP 22: peripheral myelin protein is involved in compaction of myelin on peripheral nerves
36
Charcot Marie Tooth Disease: | Symptoms?
Signs Below Knee: 1. distal muscle weakness 2. atrophy of leg below knee 3. orthopedic foot problems (hammer toe/↑arch feet)
37
DM Neuropathy: | Pathogenesis of diffuse sensory motor neuropathy?
↑Sorbitol + ↓Myoinositol In Nerves
38
DM Neuropathy: | Types of neuropathies?
1. Mononeuropathy 2. Mononeuritis Complex 3. Dif Polyneuropathy (sensory, motor, ANS, mixed) 4. Truncal (truncal sensory deficit) 5. Diabetic Amyotrophy (LS Plexus ischemia)
39
DM Neuropathy: | Presentation of diffuse sensory motor neuropathy?
burning of feet --> numbness, weakness
40
DM Neuropathy: | Prognosis of diffuse sensory motor neuropathy?
improves w/ good control of DM
41
What causes the excess sorbitol in DN?
excess glu converted to sorbitol via aldose reductase *Sorbitol Dehydrogenase: enzyme required to convert sorbitol ---> fructose; lacking in Schwann Cells, Retina, Lens, Kidneys
42
What are the consequences of excess sorbitol in DN?
Osmotic damage --> ↑osmotically active particle in Schawnn Cells, which causes: Vasculopathy and Entrapment Neuropathies
43
DM Neuropathy: | Pathogenesis of mononeuritis, mononeuritis multiplex, and diabetic ophthalmoplegia?
caused by infarct to nerves or plexus
44
Guillain Barre Syndrome: | etiology?
AI, 2-weeks post-infection with Campy, EBV, CMV, Mycoplasma
45
Guillain Barre Syndrome: | Clinical findings?
1. Paralysis 2. Radiculoneuropathy: acute + inflammatory 3. Mild paresthesia (no sensory defect) 4. Areflexia
46
Guillain Barre Syndrome: | Description of paralysis?
- ascending --> respiratory/facial DZ - progressive prox demyelination (occurs over 2-3 weeks post-infection) - symmetrical
47
Guillain Barre Syndrome: | Trx?
1. Symptoms: respiratory assistance | 2. ɣ Globulin Infusion: get rid of antibodies
48
Chronic Inflammatory Neuropathy: | Etiology?
AI inflammatory neuropathy affecting the myelin sheath
49
Chronic Inflammatory Neuropathy: | Clinical findings?
1. Paralysis (sym w/distal + prox features) 2. Severe loss of epicritic system (intact pain/temperature) 3. Conduction Block 4. Areflexia *no cranial nerve deficits or central demyelination
50
Chronic Inflammatory Neuropathy: | Path?
segmental demyelination with signs of de/re-myelination
51
Chronic Inflammatory Neuropathy: | Trx?
Steroids, Immunosuppressant, ɣGlobulin
52
Chronic Inflammatory Neuropathy: | Labs/Imaging/Biopsy?
- EMG shows ↓denervation - incr CSF protein - biopsy = segmental demyelination