Part I: spinal-cord neoplasms-intradural neoplasms

Lancet Oncol. 2007 Jan;8(1):35-45. doi: 10.1016/S1470-2045(06)71009-9.

Abstract

Intradural spinal-cord tumours are an uncommon but important consideration in the differential diagnosis of patients with back pain, radicular pain, sensorimotor deficits, or sphincter dysfunction. Intradural spinal tumours can be divided into intramedullary and extramedullary spinal-cord tumours on the basis of their anatomical relation to the spinal parenchyma. The heterogeneous cell composition of the intradural compartment allows the formation of neoplasms, arising from glial cells, neurons, and cells of spinal vasculature. Additionally, developmental tumours, metastases, and intradural extension of extradural tumours are represented. In this Review, we discuss the published work on intradural spinal-cord tumours in terms of epidemiological, radiographic, and histological characteristics. Surgical and adjuvant treatment strategies are also reviewed.

Publication types

  • Review

MeSH terms

  • Humans
  • Spinal Cord Neoplasms / classification
  • Spinal Cord Neoplasms / pathology*