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Ependymoma

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Molecular Pathology of Nervous System Tumors

Part of the book series: Molecular Pathology Library ((MPLB,volume 8))

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Abstract

Brain tumors are the most common childhood solid malignancy and the leading cause of cancer-related mortality in children. Ependymomas are among the most prevalent entities in children and show a high degree of clinical, histological, and genetic heterogeneity, which may only be explained by the underlying tumor biology. Histopathological diagnosis of ependymomas, according to the classification of the World Health Organization (WHO), is of paramount importance for clinicians to choose the most appropriate treatment option and tailor treatment intensity to disease risk. Considerable advances have been made in the past decades to cure a substantial proportion of children with these tumors. However, many children still succumb to their disease, and many survivors suffer from severe long-term cognitive, neurological, endocrinological, and psychosocial sequelae of intensive multimodal treatment including surgery and radio-chemotherapy. Furthermore, histopathological assessment is often difficult and adding molecular information to classic neuropathological assessment may likely increase diagnostic accuracy, improve risk stratification of patients, and help to identify novel therapeutic targets for an individualized treatment approach.

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Correspondence to Till Milde .

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Milde, T., Korshunov, A., Witt, O., Pfister, S.M., Witt, H. (2015). Ependymoma. In: Karajannis, M., Zagzag, D. (eds) Molecular Pathology of Nervous System Tumors. Molecular Pathology Library, vol 8. Springer, New York, NY. https://doi.org/10.1007/978-1-4939-1830-0_5

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  • DOI: https://doi.org/10.1007/978-1-4939-1830-0_5

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