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Cervical spinal root cavernoma: case report and review.

Fraser Henderson1, Daniel Carl Skipper2, Sunil Patel1

  • 1a Department of Neurosurgery , Medical University of South Carolina , Charleston , South Carolina , USA.

British Journal of Neurosurgery
|September 17, 2016
PubMed
Summary
This summary is machine-generated.

Spinal canal cavernous malformations are rare. Surgical removal of these symptomatic cervical lesions offers excellent recovery and functional restoration.

Keywords:
Cavernomacavernous malformationcervicalcervical spinedissectionlaminectomysurgery

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Area of Science:

  • Neurosurgery
  • Neurology
  • Spinal Cord Pathology

Background:

  • Spinal canal cavernous malformations are uncommon vascular anomalies.
  • Intradural extramedullary cavernomas are particularly rare, with few reported cases.
  • This study focuses on a unique case of cervical intradural extramedullary cavernoma.

Observation:

  • A 65-year-old woman presented with neck and right arm radicular pain and paresthesias.
  • The patient had a cervical intradural extramedullary cavernoma associated with a ventral cervical rootlet.
  • A PubMed search was conducted to compare this case with existing literature.

Findings:

  • The cervical cavernoma was surgically removed.
  • Histopathology confirmed the diagnosis of cavernoma.
  • The patient experienced excellent recovery with no neurological deficits post-surgery.

Implications:

  • Gross total resection is the recommended treatment for symptomatic spinal cavernous malformations.
  • Surgical outcomes for these lesions are generally favorable, with functional restoration.
  • Prompt surgical intervention for spinal cavernous malformations can lead to positive patient outcomes.