Intradural spinal teratoma: evidence for a dysembryogenic origin. Report of four cases.

Published

Journal Article

Intradural spinal teratoma is a rare tumor that can be associated with dysraphic defects. Although the origin of these tumors is traditionally thought to be secondary to primordial germ cells misplaced early in embryogenesis, the pathogenesis of intraspinal teratoma remains unclear. The authors present a series of patients in whom an intradural teratoma arose at the same site as a developmental spinal cord abnormality, including a split cord malformation, myelomeningocele, and lipomyelomeningocele. It is postulated that these lesions were the result of a dysembryogenic mechanism and were not neoplastic.

Full Text

Duke Authors

Cited Authors

  • Koen, JL; McLendon, RE; George, TM

Published Date

  • November 1998

Published In

Volume / Issue

  • 89 / 5

Start / End Page

  • 844 - 851

PubMed ID

  • 9817426

Pubmed Central ID

  • 9817426

Electronic International Standard Serial Number (EISSN)

  • 1933-0693

International Standard Serial Number (ISSN)

  • 0022-3085

Digital Object Identifier (DOI)

  • 10.3171/jns.1998.89.5.0844

Language

  • eng