Spinal cord compression and myelopathies

William F. Schmalstieg, Brian G. Weinshenker

Research output: Chapter in Book/Report/Conference proceedingChapter

Abstract

Patients with signs and symptoms of acute myelopathy require urgent neurologic evaluation focused upon the identification and management of treatable disorders. MRI of the spine is the imaging modality of choice to evaluate for a compressive lesion. When cord compression is present, surgical treatment is usually indicated. When compression is not detected, an analysis of precise lesion localization, nonneurological clinical features, MRI findings, and serologic studies narrow the differential diagnosis. The key diagnostic considerations include demyelinating, vascular, inflammatory, infectious, and paraneoplastic disorders. Empiric high-dose corticosteroid treatment is often indicated in noncompressive myelopathy; additional investigations are important to identify patients with relapsing or progressive disorders who may benefit from preventive therapies. Patients whose symptoms continue to progress after initial immunosuppressive treatment may benefit from plasmapheresis and occasionally from biopsy for definitive diagnosis.

Original languageEnglish (US)
Title of host publicationEmergency Neurology
PublisherSpringer US
Pages235-258
Number of pages24
ISBN (Electronic)9780387885858
ISBN (Print)9780387885841
DOIs
StatePublished - Jan 1 2012

Keywords

  • CNS
  • Demyelinating autoimmune disease
  • Magnetic resonance imaging
  • Myelitis
  • Spinal cord compression
  • Spinal cord diseases
  • Transverse

ASJC Scopus subject areas

  • General Medicine

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