Abstract
Ependymoma and ependymoma variants (choroid plexus papilloma and subependymoma) constitute a relatively small portion of primary childhood intracranial tumors but have generated intense controversy among clinicians. First described by Storch almost 100 years ago, but more formally recognized as a truly separate entity over 50 years ago in a monograph by Bailey and Cushing [1] ependymoma still poses unanswered basic questions regarding classification, pathology, biologic behavior, prognostic staging parameters, and optimal treatment. This chapter will review these controversies in an attempt to arrive at a rational basis for appropriate classification, staging, and management.
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Silverman, C.L., Thomas, P.R.M., Cox, W. (1990). Ependymomas. In: Deutsch, M. (eds) Management of Childhood Brain Tumors. Foundations of Neurological Surgery, vol 3. Springer, Boston, MA. https://doi.org/10.1007/978-1-4613-1501-8_15
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DOI: https://doi.org/10.1007/978-1-4613-1501-8_15
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