Non-enhancing intradural extramedullary ependymoma: A case report

Jaemin Kim; Hyunjung Kim; Hyeongju Kwon

doi:10.3348/JKSR.2020.0147

Non-enhancing intradural extramedullary ependymoma: A case report

Jaemin Kim, Hyunjung Kim, Hyeongju Kwon

Pathology

Research output: Contribution to journal › Article › peer-review

Abstract

Spinal ependymomas are generally located in the intramedullary compartment in adults. Intradural extramedullary spinal ependymomas are extremely rare. Spinal ependymomas show various contrast enhancements on MRI. In this study, we report a rare case of a 52-year-old female who had a pathologically confirmed intradural extramedullary ependymoma that showed no enhancement on MRI.

Original language	English
Journal	Journal of the Korean Society of Radiology
Volume	82
DOIs	https://doi.org/10.3348/JKSR.2020.0147
Publication status	Published - 2021 Jul

Bibliographical note

Publisher Copyright:
© 2021 The Korean Society of Radiology.

All Science Journal Classification (ASJC) codes

Radiology Nuclear Medicine and imaging

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10.3348/JKSR.2020.0147

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title = "Non-enhancing intradural extramedullary ependymoma: A case report",

abstract = "Spinal ependymomas are generally located in the intramedullary compartment in adults. Intradural extramedullary spinal ependymomas are extremely rare. Spinal ependymomas show various contrast enhancements on MRI. In this study, we report a rare case of a 52-year-old female who had a pathologically confirmed intradural extramedullary ependymoma that showed no enhancement on MRI.",

author = "Jaemin Kim and Hyunjung Kim and Hyeongju Kwon",

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year = "2021",

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AB - Spinal ependymomas are generally located in the intramedullary compartment in adults. Intradural extramedullary spinal ependymomas are extremely rare. Spinal ependymomas show various contrast enhancements on MRI. In this study, we report a rare case of a 52-year-old female who had a pathologically confirmed intradural extramedullary ependymoma that showed no enhancement on MRI.

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Non-enhancing intradural extramedullary ependymoma: A case report

Abstract

Bibliographical note

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