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Publication Name World Journal of Clinical Oncology
Manuscript ID 64760
Country Japan
Category Oncology
Manuscript Type Case Report
Article Title Anaplastic myxopapillary ependymoma: A case report and review of literature
Manuscript Source Invited Manuscript
All Author List Hiroshi Kanno, Yukiko Kanetsuna and Masamichi Shinonaga
Funding Agency and Grant Number
Corresponding Author Hiroshi Kanno, MD, PhD, Professor, Surgical Oncologist, Department of Neurosurgery, International University of Health and Welfare Atami Hospital, 13-1 East Coast, Atami 413-0012, Shizuoka, Japan. hiroshikannomd@nifty.com
Key Words Myxopapillary ependymoma; Anaplastic feature; Pathological feature; Clinical feature; Management; Case report
Core Tip Myxopapillary ependymoma (MPE) is a pathological grade I tumor that develops in the filum terminale. MPEs with anaplastic features are extremely rare; only 5 cases have shown malignancy when they relapsed. Here we report a case of MPE with anaplastic features in local late recurrence in a 46-year-old woman and review anaplastic MPE in the published literature. MPEs have the potential for malignant transformation after a long period of time despite being a pathological grade I tumor. Therefore, the possibility of malignant transformation of the MPE should be considered, and patients with MPE should be treated carefully and monitored over a long period of time.
Citation Kanno H, Kanetsuna Y, Shinonaga M. Anaplastic myxopapillary ependymoma: A case report and review of literature. World J Clin Oncol 2021; 12(11): 1072-1082
Received
2021-02-23 08:53
Peer-Review Started
2021-02-23 08:58
To Make the First Decision
Return for Revision
2021-05-04 02:41
Revised
2021-05-17 23:56
Second Decision
2021-10-09 03:25
Accepted by Journal Editor-in-Chief
Accepted by Company Editor-in-Chief
2021-10-11 01:28
Articles in Press
2021-10-11 01:28
Publication Fee Transferred
Edit the Manuscript by Language Editor
2021-09-22 09:31
Typeset the Manuscript
2021-11-17 05:59
ISSN 2218-4333 (online)
Open Access This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/Licenses/by-nc/4.0/
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