Peripheral Nervous System: Evaluation and Treatment Flashcards

1
Q

definition, mechanism, symptoms and management of radiculopathy

A

Definition: lesion of an individual spinal nerve root

Mechanism: repetitive wear and tear→ dehydration/age leads to radial fissures in the annulus fibrosus annular tear→ nucleus pulposus extrudes along the annular tear→ contained disc rupture→ with further degeneration, the nucleus pulposus protrudes beyond the perimeter → radiculopathy

  • All radiculopathies: pain in the territory supplied by the nerve root, sensory loss in the corresponding dermatome, muscle weakness or flaccid paralysis, muscle atrophy, fasciculation, decreased tendon reflexes at those muscles supplied by nerve root, vertebral column signs or symptoms
  • Lumbar radiculopathies: pain radiating from back to leg, sciatica pain exacerbated by flexion, sitting, coughing, straining

Management: Management: 80-90% spontaneously recover within 6-12wk. If hasn’t improved consider imaging +/- surgery

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2
Q

Which muscles and pattern of sensory changes are affected by each nerve root radiculopathy: C5, C6, C7, C8, L4, L5, S1

A

C5= deltoids/biceps (axillary)

C6= biceps (musculocutaneous)

C7= triceps, finger extensors (radial)

C8= finger extensors, abductors fo the 2nd and 5th fingers

L4: quads

L5: greater toe extensor

S1: plantar flexors

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3
Q

Outline the weakness type, sensory loss prevalence, etiologies of different damage patterns of peripheral nerve disease (focal, multifocal, diffuse demyelinated vs diffuse axonal)

A

Focal

  • LMN-type monoplegia
  • Motor and sensory loss
  • Sharp boundaries for sensory loss
  • Typical etiology: compressions.

Multifocal

  • More than one focal neuropathy occurring simultaneously
  • Typical etiology: autoimmune disease

Diffuse

  • Individual axons each affected simultaneously
  • Longest neurones typically most vulnerable
  • Demyelinating or axonal character
  • Typical aetiology; diabetes mellitus
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4
Q

Compare this list of features in Axonal vs demyelinating PN

A

stocking glove pattern is classic axonal degeneraton, and affects sensory more than motor. in demyelinating PN, axons have variable degrees of insulation, and are transmitting at different speeds. tends to affect motor >sensory

Axonal Peripheral Nerve Disease : Heidi’s Notes Summary

Definition: a mild, slowly progressive loss of sensory function in a stocking glove pattern

Etiology: idiopathic, DM, alcohol, thyroid, B12, SPEP, iatrogenic (chemo, amiodarone, pyridoxine) Investigations: bloodwork (TSH, T3/T4, B12, SPEP, glucose), neurophysiology NOT helpful

Management:

  • Treat underlying cause: treat DM, alcohol cessation, stop drug
  • Neuropathic pain meds: gabapentin, pregabalin, amitriptyline, topiramate
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5
Q

C7 radiculopathy vs radial neuropathy

A

Radial Neuropathy/ Saturday Night Palsy/ Honeymoon Palsy

Definition: compression along the spiral groove of the humerus

Symptoms: wrist drop due to weakness, minimal sensory loss to dorsal hand + wrist– will not affect the triceps–> if it was a C7 injury, the triceps would also be affected

Investigations: NCS for prognosis Management: usually spontaneous recovery in weeks, wrist splint

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6
Q

L5 radiculopathy vs peroneal neuropathy

A

Peroneal nerve palsy will have no radicular pain, no straight leg raise pain, no weakness of foot inversion

In L5 radiculopathy, the patient should have hip abductor and ankle inverter weakness, in addition to the foot drop.

In sciatic neuropathy, the patient should have knee flexor and plantar flexor weakness as well as foot drop. \

And in peroneal neuropathy only, the patient should have only foot drop.

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7
Q

Definition, etiology and symptoms of Guillain Barre Synrome (Neuropathy– acute inflammatory demyelinating polyneuropathy).

  • Key clinical finding?
  • investigations
  • Management
A
  • subacute demyalinating autoimmune disease
    etiology: POST INFECTION (Campylobacter jejuni, or post-influenza vaccination)
    symptoms: motor symtoms wiht ASCNEDING PATTERN, autonomic dysfinctioN(cardiac), respiratory failure ,bulbar weakness, AREFLEXIA ***

Investigations: CSF (modest protein elevation), MRI, EMG (F-WAVE LATENCY), LP: Elevated CSF protein, lower WBC and RBC

Management: IVIG, plasma exchange therapy, monitor repsiraory and cardiac function.

prognosis; typically excellent.

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8
Q

Definition, etiology, symptoms and investigations and management of mononeuritis multiplex

A

Mononeritis Multiplex

Definition: subacute onset of malfunction in multiple peripheral nerves due to damage to vessels upplying the peripheral nerves

Etiology: connective tissue diseases** MOST COMMON (polyarteritis nodosa, eGPA, GPA, cryoglobulinemia, SLE, Sjorgen, sarcoidosis), infection (HIV), Lyme, leprosy, malignancy (lymphoma)

Symptoms: patchy/asymmetric, distal>proximal pain

Investigations: Connective Tissue Disease workup, nerve/muscle biopsy, EMG/NCS

Management: treat underlying + immunosuppression

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9
Q

pain progression in mononeuritis multiplex

A

distal > proximal,

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10
Q

Read: charcot-Marie Tooth Disease (Type Ia CMTIA)

Definition: duplication of PMP22 gene, hereditary demyelinating neuropathy

Etiology: autosomal dominant, duplication of PMP22 gene (codes for a structural protein in the transmembrane space of compact myelin)

Epi: 1:10000; childhood onset (typically described as being clumsy, non-athletic)

Symptoms: distal weakness, distal atrophy of hands and feet (interosseous wasting, claw hand, hammertoes, pes cavous, Champagne bottle legs)

Sensory symptoms tend not to occur early on.

Investigations: genetic testing, neurophysiology (demyelinating neuropathy, diffuse)

Management: ankle surgery is common due to repeated injury

Prognosis: normal life expectancy, often maintain ambulation

A

Read: Herreditary Neuropathy with Liability to Pressure Palsies

Hereditary Neuropathy with Liability to Pressure Palsies (HNPP)

Definition: deletion of PMP22, hereditary demyelinating neuropathy

Unusual example of diffuse neuropathy causing focal neuropathy symptoms.

The strange myelin is susceptible to compression injury

Repeated injury to nerves caused after short compression.

Etiology: autosomal dominant, deletion of PMP22 gene

Epi: 1:200000

Symptoms: diffuse neuropathy that produce focal neuropathy symptoms due to susceptible of myelin to compression injuries, usually more motor and no pain

Investigations: neurophysiology findings are worse than clinical symptoms

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11
Q

Identify which roots innervate the biceps, brachioradialis, triceps, knee jerk, and ankle jerk reflexes

A

Biceps– musculocutaneus

Triceps– radial nerve

Brachioradialis– radial nerve

The knee jerk reflex is mediated by the L3 and L4 nerve roots, mainly L4. Insult to the cerebellum may lead to pendular reflexes. Pendular reflexes are not brisk but involve less damping of the limb movement than is usually observed when a deep tendon reflex is elicited.

​​The ankle jerk reflex is mediated by the S1 nerve root. The plantar reflex (Babinski) is tested by coarsely running a key or the end of the reflex hammer up the lateral aspect of the foot from heel to big toe. The normal reflex is toe flexion.

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