Ependymoma

Last revised by Pardeep Singh Villocero Basi on 2 Feb 2025

Ependymomas represent a relatively broad group of glial tumours with ependymal differentiation. They often arise from or near the lining of the ventricles of the brain or the central canal of the spinal cord but also occur within the brain parenchyma. 

The unqualified term "ependymoma" should be used somewhat carefully as the entities included in this term vary in the literature and clinical practice. Generally, it is best to be specific, using the terminology of the WHO classification (see below). The five tumours included under the heading of "ependymal tumours" vary greatly in location, demographics, imaging features, histology, molecular characteristics, treatment and prognosis. They are, therefore, best thought of and discussed as separate entities.

Overall, ependymomas have a bimodal distribution, with peaks in childhood and again later in adulthood. The incidence of different tumour types and locations varies greatly, with posterior fossa ependymomas predominating in childhood and spinal ependymomas in adulthood 20-21.

Ependymal tumours can occur anywhere within the neuraxis; however, the distribution, histology and molecular characteristics, including DNA methylation profiling, are fairly site-dependent. As such the 5th edition (2021) WHO classification divides ependymal tumours into five distinct entities; three based on location, further subdivided according to molecular characteristics, and two other specific entities 11,13,15,18.

Cases and figures

  • Case 1: posterior fossa ependymoma
  • Case 2: supratentorial
  • Case 3: spinal ependymoma
  • Case 5: myxopapillary ependymoma
  • Case 4: subependymoma
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