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Wheeless' Textbook of Orthopaedics
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Primary Spinal Cord Neoplasia



- Intrameduallary tumors:
    - infiltrate or compress the spinal cord so gradually that they may grow to considerable size before detection;
          - are glial in origin (except for the rare hemangioblastoma)
    - ependymomas:
          - commonly arises in the conus medullaris
          - tends to be a discrete lesion which can be excised;
    - astrocytomas
          - potential for malignant degeneration resembling cerebral GBM;
          - extremely difficult/impossible to excise

- Intradural, Extramedullary tumors:
    - usually benign, slow growing, and well circumscribed
    - arise from the swan cells of the proximal nerve roots
    - spinal meningiomas occur 10x more frequently in women;
    - may be completely excised, usually not radiosensitive;
    - include benign meningioma and neurilemmoma and neurofibroma;
    - local and radicular pain is an early symptom;
    - spinal cord deficit develops gradually & is often not dx'ed until Brown Sequard Syndrome deficit becomes evident;
    - myeography demonstates the tumor;
    - nerve roots in the thoracic region may be sectioned for better exposure, but damage to radicular arteries must be avoided;





The treatment of primary vertebral tumors by radical resection and prosthetic vertebral replacement.

Primary neoplasms of the cervical spine. Diagnosis and treatment of twenty-three patients.

Primary tumors of the spine.
      JN Weinstein and RF McLain.   Spine Vol 12. 1987 p 843-851.

Orthopaedic aspects of intraspinal tumors in infants and children.
      MO Tachdjian and DD Matson.   JBJS. Vol 47-A. 1965. p 223-248.

Intramedullary spinal cord tumors presenting as scoliosis.
      N. Citron et al.   JBJS. Vol 1984-B. Vol 66-B. p 513-517.
 











Original Text by Clifford R. Wheeless, III, MD.