Extradural spine tumors in the pediatric population are a relatively rare occurrence and constitute a heterogeneous group of pathologies. Management is dictated by both specific tumor pathology, as well as the severity of neurologic symptoms at presentation. Because of their rarity, management of spinal cord compression (SCC) secondary to epidural spinal tumors in children remains controversial and includes decompressive and resective surgery, radiotherapy, chemotherapy, or a combination of the three. © Springer-Verlag Berlin Heidelberg 2006.
CITATION STYLE
Kazina, C., & McDonald, P. (2006). Epidural spinal tumors in children. In Neuro-Oncology of CNS Tumors (pp. 575–581). Springer Berlin Heidelberg. https://doi.org/10.1007/3-540-31260-9_48
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