| Literature DB >> 27092234 |
Dean Petersen1, Reidar P Lystad2.
Abstract
BACKGROUND: Spinal intramedullary ependymomas are very rare and occur more commonly in the cervical and upper thoracic regions. These neoplasms tend to manifest in young adulthood, and patients typically present with mild clinical symptoms without objective evidence of neurologic deficits. The mean duration of symptoms is 40 months until the lesion is diagnosed. CASEEntities:
Keywords: Chiropractic; Filum terminale; Myxopapillary ependymoma; Neoplasm; Spinal cord
Year: 2016 PMID: 27092234 PMCID: PMC4834819 DOI: 10.1186/s12998-016-0094-y
Source DB: PubMed Journal: Chiropr Man Therap ISSN: 2045-709X
Fig. 1Sagittal fat suppressed T1-weighted (a) and T2-weighted (b) magnetic resonance images of the lumbosacral spine. A heterogeneous, predominantly cystic, intramedullary space-occupying lesion measuring 2.5 × 1.2 cm is present within the filum terminale at L2/3 level (green arrow). Additional findings include a transitional lumbosacral vertebra (lumbarisation of S1), dehydration of the L5/S1 intervertebral disc with a posterior disc bulge, and a hemangioma in the vertebral body of L5. The remainder of the spinal cord and conus medullaris, lower thoracic and lumbosacral vertebrae, intervertebral disc spaces, and paraspinal soft tissues appear normal