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dc.contributor.authorRutherford, Scott A
dc.contributor.authorLinton, Kim M
dc.contributor.authorDurnian, Jonathan M
dc.contributor.authorCowie, Richard A
dc.date.accessioned2009-07-06T15:43:51Z
dc.date.available2009-07-06T15:43:51Z
dc.date.issued2006-01
dc.identifier.citationEpidural meningioma of the sacral canal. Case report. 2006, 4 (1):71-4 J Neurosurg Spineen
dc.identifier.issn1547-5654
dc.identifier.pmid16506469
dc.identifier.doi10.3171/spi.2006.4.1.71
dc.identifier.urihttp://hdl.handle.net/10541/72624
dc.description.abstractSpinal meningiomas are reported infrequently as pure epidural tumors, and they are rarely located at the caudal end of the spine. The unique combination of a wholly epidural tumor confined entirely to the sacral canal has not been previously described. The authors describe the case of a 29-year-old man who presented with coccygeal and left-sided S2-4 dermatomal pain. Examination confirmed sensory loss in the same distribution. A magnetic resonance image revealed an enhancing mass lesion in the sacral canal scalloping the bone at S-2 and S-3. An apparent complete resection was performed. Intraoperatively the authors observed an entirely epidural tumor with a small dural attachment at the most caudal end of the thecal sac. Histological examination confirmed that the tumor was an atypical meningioma. A local recurrence developed within 1 year of surgery, and the patient underwent a hemisacrectomy for tumor removal. An additional recurrence in the lumbosacral spine and multiple pulmonary metastases developed thereafter. In addition to the unique nature of this case, the authors also observed a tumor behaving in a far more aggressive fashion than its histological findings would suggest. This adds to the differential diagnosis of tumors occurring in the sacral canal.
dc.language.isoenen
dc.subjectMeningeal Canceren
dc.subjectSpinal Cord Canceren
dc.subject.meshAdult
dc.subject.meshEpidural Space
dc.subject.meshHumans
dc.subject.meshMagnetic Resonance Imaging
dc.subject.meshMale
dc.subject.meshMeningeal Neoplasms
dc.subject.meshMeningioma
dc.subject.meshNeoplasm Recurrence, Local
dc.subject.meshPrognosis
dc.subject.meshSacrococcygeal Region
dc.subject.meshSpinal Cord Neoplasms
dc.titleEpidural meningioma of the sacral canal. Case report.en
dc.typeArticleen
dc.contributor.departmentDepartment of Neurosurgery, Hope Hospital, Salford, Manchester, United Kingdom. scott.rutherford@srht.nhs.uken
dc.identifier.journalJournal of Neurosurgery. Spineen
html.description.abstractSpinal meningiomas are reported infrequently as pure epidural tumors, and they are rarely located at the caudal end of the spine. The unique combination of a wholly epidural tumor confined entirely to the sacral canal has not been previously described. The authors describe the case of a 29-year-old man who presented with coccygeal and left-sided S2-4 dermatomal pain. Examination confirmed sensory loss in the same distribution. A magnetic resonance image revealed an enhancing mass lesion in the sacral canal scalloping the bone at S-2 and S-3. An apparent complete resection was performed. Intraoperatively the authors observed an entirely epidural tumor with a small dural attachment at the most caudal end of the thecal sac. Histological examination confirmed that the tumor was an atypical meningioma. A local recurrence developed within 1 year of surgery, and the patient underwent a hemisacrectomy for tumor removal. An additional recurrence in the lumbosacral spine and multiple pulmonary metastases developed thereafter. In addition to the unique nature of this case, the authors also observed a tumor behaving in a far more aggressive fashion than its histological findings would suggest. This adds to the differential diagnosis of tumors occurring in the sacral canal.


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