LE Neuropathies- Shappy Flashcards
(51 cards)
Parts of the PNS
Motor
Sensory
Autonomic
Neurapraxia
caused by mild ischemia
-segmental demylination blocking condition
Axonotmesis
Prolonged compression and necrosis
- axon damage connective tissue intact
Neurotmesis
Complete severance of axon and distruption of connective tissue
- gun shot, stab (can be surgical) or avulsion, amputations
- muscle fibers atrophy due to loss of trophic stubstances
Causes of PN injury
compression/ trauma, heredity, infections, toxins, metabolic, etc
Demylination
typically segmental
-damage to the mylin sheath around the nerve loosing the velocity of conduction
Degeneration (of PN)
typically more severe injury
- Anterograde or Wallerian degerneration (dead at the distal end)
- ex. foot dangling off the bed and having a nerve compression If the nerve is severed then Wallerian degeneration. If the axon stays intact, not Wallerian
Regeneration
Slow process, axonal sprouting
can get lost and not find correct endoneurial tube
if there is connective tissue, more likely of the target tissues have the connection to have the regrowth
Reinnervation
Can occur when adjacent neuron innervates muscle fibers of injured neuron, collateral sprouting
Mononeuropathy
single PN injured
Polyneuropathy
several PN injured
Radiculoneuropathy
(or Radiculopathy)
Nerve root injury
Polyradiculitis
infection creating inflammation of several nerve roots
Myopathy
Motor endplate injury
synpse issue
Signs and Symptoms of Peripheral Dysfunction
(Sensory)
tingling, numbness, burning, etc
- peripheral distribution
- nerve root (distal first, stocking glove distribution)
Signs and Symptoms of Peripheral Dysfunction
(Motor)
weakness, hypotonia, flaccid
- paresis or paralysis- peripheral distrubution
- weakness-myotome distributions of that spinal nerve
Signs and Symptoms of Peripheral Dysfunction
(automonic)
Vascular, sweating, hair, skin
Charcot-Marie-Tooth (CMT) Disease
Hereditary motor and sensory neuropathy or peroneal muscular atrophy; Charcot foot- the foot’s intrinsic muscles are wasting which creates a high arch and clawed toes
- distal limb muscle wasting and weakness
- skeletal deformities
- distal sensory loss
- DTR abnormalities
- balance issues which makes them walk farther appart have a large base of support
- looks like they are walking on glass
Charcot Foot
Chromosomal defect; high arch and toes curls
CMT Pathology
mutation in the proteins
-Schwaan cell demyelination along with hypertrophic onion bulb formation
onion bulb
(like seen in CMT)
palpable enlarged peripheral nerves due to Schwann cells and precesses attempting to remyelinate damaged nerves
Clinical Presentation of CMT
Pes Cavus and hammer toes
Weakness in DF and EVER, foot drop, and steppage gait
Wasting of intrinsic muscles (because the foot is holding in one position)
Loss of proprioception and cutaneous sensation (tingling and burning sensations present); having balance problems
CMT Diagnosis
EMG studies
- decresed NCV- both motor and sensory
- axonal degeneration or demyelination on nerve biopsy
CMT Treatment
Can not fix the cause, only treat the symptoms
- footdrop- bracing, remebering skin care due to the insensate feet
- gait training
- ROM exercises (can try, but this is something that the patient will need to learn to do everyday in order to get to neurtal)
- strengthening has questionable effects
- overall conditioning
- balance training- work on ways to compensate