Pediatric intramedullary spinal cord tumors. Critical review of the literature
- PMID: 10066016
- DOI: 10.1007/s003810050321
Pediatric intramedullary spinal cord tumors. Critical review of the literature
Abstract
The objective of this review was to analyze the literature on the management of intramedullary spinal cord tumors to determine whether enough information was available for treatment guidelines to be established. Using standard computerized search techniques, databases containing medical literature were queried for keywords related to intramedullary spinal cord tumors, beginning in 1966. Of the 445 articles published in English and with potential relevance, only 75 articles were included in the final analyses. Based on the strength of their recommendations for the treatment of this controversial condition, articles were divided into class I, class II and class III data. There were no class I studies related to any aspect of the treatment of intramedullary spinal cord tumors. Based on this critical review of literature, gross total removal of an ependymoma confirmed by immediate postoperative magnetic resonance imaging and adjunctive treatment for high-grade tumors using radiotherapy, with or without chemotherapy, can be recommended as standards of therapy. With the strength of a guideline, radiotherapy should be withheld after gross total removal of intramedullary ependymomas and radical resection of low-grade intramedullary astrocytomas. The use of intraoperative ultrasonography and evoked potentials, important surgical adjuncts, can also be considered guidelines. The radical resection of intramedullary low-grade astrocytomas is an option.
Comment in
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Pediatric intramedullary spinal cord tumors.Childs Nerv Syst. 1999 Sep;15(9):436-8. doi: 10.1007/s003810050431. Childs Nerv Syst. 1999. PMID: 10501998 No abstract available.
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