Cargando…

Extramedullary Conus Ependymoma Involving a Lumbar Nerve Root with Filum Terminale Attachment

PURPOSE: In the current report, we describe a case of an extramedullary ependymoma involving a lumbar nerve root near conus medullaris. Spinal ependymomas commonly present as intramedullary tumors in the cervical or thoracic cord or as tumors arising from the conus medullaris or the filum terminale....

Descripción completa

Detalles Bibliográficos
Autores principales: Moriwaki, Takashi, Iwatsuki, Koichi, Ohnishi, Yu-ichiro, Ninomiya, Koshi, Yoshimine, Toshiki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Libertas Academica 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4666522/
https://www.ncbi.nlm.nih.gov/pubmed/26648765
http://dx.doi.org/10.4137/CCRep.S24719
Descripción
Sumario:PURPOSE: In the current report, we describe a case of an extramedullary ependymoma involving a lumbar nerve root near conus medullaris. Spinal ependymomas commonly present as intramedullary tumors in the cervical or thoracic cord or as tumors arising from the conus medullaris or the filum terminale. In this case, we showed an extramedullary conus ependymoma involving a lumbar nerve root with filum terminale attachment. CASE PRESENTATION: A 69-year-old woman presented with lower back pain, but without sensory disturbance or motor weakness in her lower extremities. CLINICAL ASSESSMENT: Magnetic resonance imaging revealed an intradural mass at T12–L1 at the conus medullaris, which was totally resected. Histopathology revealed a non-myxopapillary ependymoma (WHO grade 2). Postoperatively, the patient did well and displayed no neurological deficits. Moreover, no radiotherapy was required. CONCLUSIONS: This report documented a rare case of intradural extramedullary ependymoma located at the conus medullaris, involving the lumbar nerve root, and attached to the filum terminale. Although extramedullary ependymomas at this region are more frequently classified as myxopapillary, histopathological examination revealed this tumor as a non-myxopapillary ependymoma.