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

6Citations
Citations of this article
8Readers
Mendeley users who have this article in their library.

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.

Cite

CITATION STYLE

APA

Zhao, L., Jiang, Y., Wang, Y., Bai, Y., Liu, L., & Li, Y. (2021). Case Report: Sellar Ependymomas: A Clinic-Pathological Study and Literature Review. Frontiers in Endocrinology, 12. https://doi.org/10.3389/fendo.2021.551493

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free