Case Report: Sellar Ependymomas: A Clinic-Pathological Study and Literature Review

Front Endocrinol (Lausanne). 2021 Jun 8:12:551493. doi: 10.3389/fendo.2021.551493. eCollection 2021.

Abstract

Ependymomas are primary glial tumors arising from cells related to the ependymal lining of the ventricular system. They are classified into at least nine different molecular subtypes according to molecular phenotype, histological morphology, and tumor location. Primary sellar ependymoma is an extremely rare malignancy of the central nervous system, with only 12 known cases reported in humans. We herein report a case of ependymoma located at the pituitary region in a 44-year-old female patient and discuss the molecular subtype, natural history, clinical presentation, radiological findings, histological features, immunohistochemical characteristics, ultrastructural examinations, treatment, and prognosis of sellar ependymoma. This case report may serve as a helpful reference for clinicians and radiologists in clinical practice.

Keywords: diagnosis; ependymoma; molecular subtype; pituitary tumor; sellar ependymoma; treatment.

Publication types

  • Case Reports
  • Review

MeSH terms

  • Adult
  • Ependymoma / diagnostic imaging
  • Ependymoma / pathology*
  • Female
  • Humans
  • Magnetic Resonance Imaging
  • Pituitary Neoplasms / diagnostic imaging
  • Pituitary Neoplasms / pathology*