Lesson 25 Flashcards

1
Q

Types of syndromes

A

Radicular syndrome

Plexus syndromes

Nerve trunk syndromes

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2
Q

Clinical manifestations

A

Sensory:
- pain, numbness, reflex alterations

Motor
- Paralysis, hypotonia, atrophy, weakness

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3
Q

Radicular syndrome

A

Nerve root alterations due to tumours or hernias

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4
Q

Plexus syndromes

A

Nerve plexus alterations

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5
Q

Nerve trunk syndrome

A

Can be divided into three groups:

Mononeuropathies: mechanical lesion of one nerve

Multi-neuropathies: asymmetric ischemic lesion of different
nerves

Polyneuropathies: symmetric lesion of different nerves

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6
Q

Autonomic nervous system produce clinical manifestation at the level of effector organs

A
  • Cardiovascular: tachycardia vs bradycardia
  • Digestive system: increase vs decrease of gastrointestinal motility
  • Urinary system: urinary retention vs hyperactive bladder
  • Eye: mydriasis vs miosis
  • Reproductive system: impotence vs priapism; ejaculation disorders
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7
Q

Concept of neuropathies

A

A set of disorders that affect the
peripheral nerves.

  • Quite common, usually painful, sometimes debilitating, rarely lethal
  • Acquired or inherited
  • Systemic or localized affection.

Syndromes involving the motor system affect the anterior motor neuron, its axon, the neuromuscular junction and muscle fibers.

Peripheral nerves: Sensory, motor and autonomic fibers (mixed nerves).

Neuropathies may affect the cell body, axon or myelin.

Motor nerves:
- Usually large diameter
- Myelinated

Sensory nerves may be:
- Large diameter: proprioception and vibration

-Intermediate diameter and myelinated fibres or non-myelinated fibres: pain and temperature.

Autonomic nerves:
- Small diameter

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8
Q

NEUROPATHIES
35
Classification
Based on onset and evolution

A

Acute:
- progress in three weeks
- (guillain-barre syndrome or polyneuropathies with collagenosis)

Sub-acute:
- Progress in four weeks

Chronic:
- Progress in more than one month
- (diabetic neuropathy, amiloidosis neuropathy, toxic or nutritional neuropathy, inherited neuropathies).

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9
Q

NEUROPATHIES
36
Classification
Based on functional impairment

A
  • Pure motor, it affects motor nerves.
  • Pure sensory, it affects sensory nerves.
  • Autonomic, it affects autonomic nerves.
  • Motor and sensory, it affects mixed nerves.
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10
Q

NEUROPATHIES
37
Type of lesions
Parenchymal lesions

A

The neuron or Schwann cells suffer degeneration:

Axonal degeneration: neuronal body and axon are primarily affected.

Wallerian degeneration: disorganization of the axon and myelin.

Demyelination: Occurs without affecting the axon

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11
Q

Causes of neuropathies

A

Infectious causes
* Local infections, bacterial or viral.
* Polyneuritis as a complication of an infection (mumps).
* Bacterial toxins with affinity for CNS (diphtheria, tetanus).

Post-infectious polyneuropathies
* Guillain-Barré syndrome

Toxics
* Mercury, lead, arsenic

Nutritional deficiency
* Vitamin deficiency, alcoholism, liver impairment.

Trauma
* Physical injuries

Connective tissue diseases and related disorders
* They are due to serum protein alterations (systemic lupus, cancer)

Genetic disorders
* Hereditary radicular sensory neuropathies (Charcot–Marie–tooth
disease)

Pure vascular disorders
* Collagen disorders, diabetes mellitus

Unknown origin
polyneuropathies

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12
Q

Motor clinical manifestations

A

Muscular weakness

Muscular atrophy

Hypotonia

Areflexia

Paralysis

Muscular cramps

Resting and action tremor

Fasciculations

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13
Q

Non-motor clinical manifestations

A

Gastrointestinal disorders

Sweating disorders

Skin and glands atrophy

Bladder functionality disorders

Circulatory disorders

Body temperature alterations

Heart rate/respiratory rate alterations

Erectile dysfunction

Pain

Plantar ulcers

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14
Q

Positive sensory clinical manifestations

A
  • Prick
  • Tingle
  • Swelling (feeling)
  • Pain
  • Electric shock
  • Burning
  • Frozen
  • Oppression
  • Pulsation or vibration
  • Hyperalgesia
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15
Q

Negative sensory clinical manifestations

A
  • Imbalance
  • Proprioception
  • Anaesthesia / hypoesthesia
  • Somnolence
  • Loss of sensitivity
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16
Q

NEUROPATHIES
Complications

A

Impaired motor function
- Weakness and paralysis, affects the lower limbs the soonest and to the most severe extent

  • Slow-occurring muscle atrophy: Due to disuse and denervation
  • Degeneration and muscular lesions:
  • Starts after 6-12 m, lasts 3-4y

Sensory lesions
- Ulcers
- Amputations

Deformities and trophic lesions