“…From a clinical viewpoint, the characteristics of teratomas are no different from those of other slow-growth intramedullary tumours; their clinical history is usually lengthy and ingravescence is gradual; the topographical distribution of algesic, motor and sensory disorders is related to the site. Dys-raphic malformations such as spina bifida, diastematomyelia, and tethered cord are associated with teratomas in about 15 % of the cases [1,7,12,21,33,40,44,46,51].…”