Description

Book Synopsis
This book provides research on ependymomas, a rare brain tumor that arises from the ependymal cells of the intra-ventricular central nervous system (CNS) parenchyma with a propensity to affect both children and adults. Ependymomas account for only 1.9% of all primary brain and CNS tumors. Chapter One discusses the prognosis and outcomes in patients with ependymal tumors. Chapter Two investigates the effects of gender, age, race, tumor grade, and treatment on clinical outcomes of ependymoma diagnosed patients. Chapter Three examines survival rates, and prognostic factors. Chapter Four contains a contemporary review of the literature and an evidence-based systematic review about intraspinal ependymomas (ISE). Chapter Five reviews literature on ependymal neoplasms arising in the setting of hereditary tumor syndromes. Chapter Six discusses the current management of pediatric ependymomas and examines evolving biological data.

Ependymomas: Prognostic Factors, Treatment

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    A Hardback by Raquel Fowler

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      Book details

      Published 1 February 2016
      ISBN-13 9781634844055
      978-1634844055
      ISBN-10 163484405X
      Also in:
      Oncology

      Description

      Book Synopsis
      This book provides research on ependymomas, a rare brain tumor that arises from the ependymal cells of the intra-ventricular central nervous system (CNS) parenchyma with a propensity to affect both children and adults. Ependymomas account for only 1.9% of all primary brain and CNS tumors. Chapter One discusses the prognosis and outcomes in patients with ependymal tumors. Chapter Two investigates the effects of gender, age, race, tumor grade, and treatment on clinical outcomes of ependymoma diagnosed patients. Chapter Three examines survival rates, and prognostic factors. Chapter Four contains a contemporary review of the literature and an evidence-based systematic review about intraspinal ependymomas (ISE). Chapter Five reviews literature on ependymal neoplasms arising in the setting of hereditary tumor syndromes. Chapter Six discusses the current management of pediatric ependymomas and examines evolving biological data.

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