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Related Experiment Videos

Bilateral high radial nerve compressions: a case report.

A Chuangsuwanich1, S Muangsombut, T Sangruchi

  • 1Department of Surgery, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand.

Journal of the Medical Association of Thailand = Chotmaihet Thangphaet
|August 10, 2000
PubMed
Summary

This case study details bilateral high radial nerve compression in a 40-year-old woman caused by the radial collateral artery. Surgical intervention with sural nerve grafts successfully restored normal radial nerve function.

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Area of Science:

  • Neurology
  • Vascular Surgery
  • Orthopedic Surgery

Background:

  • High radial nerve compression is rare, especially from non-traumatic vascular causes.
  • Vascular compression of peripheral nerves can lead to significant neurological deficits.
  • The radial collateral artery is a potential, though infrequently reported, source of nerve entrapment.

Observation:

  • A 40-year-old woman presented with symptoms of bilateral high radial nerve compression.
  • Initial conservative treatment failed, necessitating surgical exploration.
  • Operative findings revealed two distinct compression sites on the right radial nerve, caused by branches of the radial collateral artery.

Findings:

  • Resection of the constricted nerve segments and interposition with a sural nerve graft was performed on the right side.

Related Experiment Videos

  • A similar presentation and surgical intervention (sural nerve graft after failed neurolysis) were required for the left radial nerve one year later.
  • Complete recovery of radial nerve function was observed in both instances within one year post-surgery.
  • Implications:

    • This case highlights the radial collateral artery as a potential cause of bilateral high radial nerve compression.
    • It underscores the importance of considering vascular anomalies in the differential diagnosis of radial nerve entrapment.
    • Successful surgical management with nerve grafting offers a viable treatment option for this rare condition.