Study Design. The present study illustrates a rare case of ependymoma
of the spinal cord. Objectives. An encapsulated intradural extramedull
ary ependymoma of the cervicothoracic spinal cord in a 24-year-old wom
an is reported. Summary of Background Data. Ependymoma is a glial tumo
r arising in the central nervous system. Intradural extramedullary epe
ndymoma of the spinal cord is rare, and two cases were reported previo
usly. Methods. The woman presented with myelopathy below C6. Magnetic
resonance imaging showed an intradural tumor from C4 to T3 and no othe
r lesion in the central nervous system, At surgery, the extramedullary
tumor apparently was not attached to the spinal cord or dura mater. G
ross total removal was easily achieved under the operating microscope.
Results. Histologic examination revealed the encapsulated tumor as an
anaplastic ependymoma. Almost complete neurologic recovery was obtain
ed. Conclusion. The encapsulated appearance, lack of an apparent attac
hment to the central nervous system, and absence of signs of the prima
ry neoplastic process within the brain or spinal cord suggested that t
he tumor arose from ectopic ependymal cells.