Intradural spinal teratoma is a rare tumor that can be associated with dysr
aphic 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 pres
ent a series of patients in whom an intradural teratoma arose at the same s
ite as a developmental spinal cord abnormality, including a split cord malf
ormation, myelomeningocele, and lipomyelomeningocele. It is postulated that
these lesions were the result of a dysembryogenic mechanism and were not n
eoplastic.