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Erschienen in: Journal of Neuro-Oncology 2/2009

01.09.2009 | Case Report

Clinicopathologic features of recurrent dysembryoplastic neuroepithelial tumor and rare malignant transformation: a report of 5 cases and review of the literature

verfasst von: Wilson Z. Ray, Spiros L. Blackburn, Sandro Casavilca-Zambrano, Carlos Barrionuevo, Jose E. Orrego, Hugo Heinicke, Joshua L. Dowling, Arie Perry

Erschienen in: Journal of Neuro-Oncology | Ausgabe 2/2009

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Abstract

Dysembryoplastic neuroepithelial tumors (DNETs) have traditionally been viewed as benign “quasihamartomatous” tumors widely considered curable with surgery alone. More recently, case reports have described malignant gliomas arising after irradiation and recurrences following subtotal or even gross total resection. Herein, we describe five cases of DNET with recurrences 2–7 years after resection. Although the radiology was often alarming (e.g., new ring enhancing mass), the pathology remained benign in most cases. Nonetheless, a probably radiation induced anaplastic astrocytoma was encountered in one case 7 years after therapy. These findings suggest that these patients may need closer follow-up than initially suggested, lending further support to the notion that this tumor behaves more like a benign neoplasm, rather than a dysplastic or hamartomatous lesion.
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Metadaten
Titel
Clinicopathologic features of recurrent dysembryoplastic neuroepithelial tumor and rare malignant transformation: a report of 5 cases and review of the literature
verfasst von
Wilson Z. Ray
Spiros L. Blackburn
Sandro Casavilca-Zambrano
Carlos Barrionuevo
Jose E. Orrego
Hugo Heinicke
Joshua L. Dowling
Arie Perry
Publikationsdatum
01.09.2009
Verlag
Springer US
Erschienen in
Journal of Neuro-Oncology / Ausgabe 2/2009
Print ISSN: 0167-594X
Elektronische ISSN: 1573-7373
DOI
https://doi.org/10.1007/s11060-009-9849-9

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