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Idiopathic spinal accessory nerve palsy. A case report.

N N Sergides1, D D Nikolopoulos, I G Polyzois

  • 1Orthopaedic Department, Central Clinic of Athens, Diagnostic and Treatment Center, Asklepiou 31 STR, ZC 10680, Athens, Greece.

Orthopaedics & Traumatology, Surgery & Research : OTSR
|June 29, 2010
PubMed
Summary

Idiopathic spinal accessory nerve palsy, causing trapezius muscle paralysis, is extremely rare. This case highlights an isolated instance in a 42-year-old male without trauma or surgery, confirmed by electromyography.

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Area of Science:

  • Neurology
  • Neurosurgery
  • Electromyography

Background:

  • Spinal accessory nerve palsy often results from iatrogenic causes, trauma, infection, or tumors, leading to trapezius muscle dysfunction.
  • Idiopathic cases, without a clear underlying cause, are exceptionally uncommon in medical literature.

Observation:

  • A 42-year-old Caucasian male presented with isolated, unilateral paralysis of his ipsilateral trapezius muscle.
  • The patient had no history of trauma, surgery, infection, or tumor that could explain the nerve palsy.

Findings:

  • Electromyographic (EMG) studies confirmed the diagnosis of idiopathic paralysis.
  • The paralysis specifically affected the distal segment of the spinal accessory nerve, impacting the trapezius muscle.

Implications:

  • This case expands the understanding of idiopathic spinal accessory nerve palsy, suggesting it may occur without identifiable triggers.
  • Highlights the importance of electromyography in diagnosing rare neurological conditions affecting cranial nerves.
  • Contributes to the differential diagnosis of isolated trapezius muscle weakness.