Primary intradural extramedullary ependymoma - Case report and review of the literature

Citation
H. Duffau et al., Primary intradural extramedullary ependymoma - Case report and review of the literature, SPINE, 25(15), 2000, pp. 1993-1995
Citations number
18
Categorie Soggetti
Neurology
Journal title
SPINE
ISSN journal
03622436 → ACNP
Volume
25
Issue
15
Year of publication
2000
Pages
1993 - 1995
Database
ISI
SICI code
0362-2436(20000801)25:15<1993:PIEE-C>2.0.ZU;2-8
Abstract
Study Design, The authors report the ninth case in the literature of a prim ary intradural extramedullary ependymoma of the spinal cord. Objective. To discuss surgical treatment and the physiopathologic hypothesi s of this localization on the basis of the results of the present study and a review of the literature. Summary of Background Data. Ependymoma is a glial tumor known to arise in t he central nervous system. Intradural extramedullary location of this neopl asm has been exceptionally described previously. Methods. A 43-year-old woman was admitted to the authors' institution with an history of progressive paraplegia, Neurologic examination showed sensory loss below T1 and bladder disturbances. Magnetic resonance imaging reveale d an enhanced thoracic intradural extramedullary tumor, extending from T1-T 8. No other lesion in the central nervous system was found. Emergency surgi cal resection was performed. Results. Surgery gave confirmation of an encapsulated extramedullary tumor without attachment to the spinal cord or to the dura mater. Total removal w as achieved under microscope, The postoperative course was uneventful, with complete neurologic recovery 3 months later. The patient has been well for 24 months of follow-up evaluation, without evidence of recurrence on magne tic resonance images. Histologic examination revealed the tumor as a benign ependymoma.; Conclusion. The encapsulated feature, the lack of attachment to the central nervous system, and the absence of other neoplastic processes within the b rain or the spinal cord suggested that this lesion is a primary tumor.:deve loped from ectopic ependymal cells.