CC BY-NC-ND 4.0 · Asian J Neurosurg 2017; 12(04): 731-734
DOI: 10.4103/ajns.AJNS_45_15
Case Report

Occipital intraparenchymal myxopapillary ependymoma: Case report and literature review

Tushit Mewada
Department of Neurosurgery, G B PANT Institute of Postgraduate Medical Education and Research, New Delhi
,
Ishu Bishnoi
Department of Neurosurgery, G B PANT Institute of Postgraduate Medical Education and Research, New Delhi
,
Hukum Singh
Department of Neurosurgery, G B PANT Institute of Postgraduate Medical Education and Research, New Delhi
,
Daljit Singh
Department of Neurosurgery, G B PANT Institute of Postgraduate Medical Education and Research, New Delhi
› Author Affiliations

Myxopapillary ependymoma (MPE) is a histological variant of ependymoma found in the conus medullaris or filum terminale region. Intracranial occurrence of the tumor is a rarity. The most characteristic histological feature of myxopapillary tumors is the abundance of intercellular and perivascular mucin and the arborizing vasculature, which tends to form papillae. We are reporting a 14-year-old patient presented with seizures caused by the right occipital region intraparenchymal lesion. Histopathology confirmed it to be MPE. Lesion was excised completely. Literature reviews on the topic are discussed regarding the histological findings, natural history, and outcome of surgically treated MPE. This is the fifth reported case of cerebral intraparenchymal primary MPE.



Publication History

Article published online:
20 September 2022

© 2017. Asian Congress of Neurological Surgeons. This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/)

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