Myxopapillary Ependymoma of the Spinal Cord in Adults: a Report of Personal Series and Review of Literature

• Main Authors: Ibrahim Omerhodžić, Mirza Pojskić, Krešimir Rotim, Bruno Splavski, Lukas Rasulić, Kenan I. Arnautovic
• Format: Article
• Language: English
• Published: Sestre Milosrdnice University hospital, Institute of Clinical Medical Research 2020-01-01
• Series: Acta Clinica Croatica
• Subjects: Myxopapillary ependymoma; Gross total resection; Surgical technique; Tumor classification
• Online Access: https://hrcak.srce.hr/file/354160
• ISSN: 0353-9466; 1333-9451

Myxopapillary ependymomas (MPE) of the spinal cord are slow-growing benign tumors most frequently found in adults between 30 and 50 years of age. They arise from the ependyma of the filum terminale and are located in the area of the medullary conus and cauda. The recommended treatment option is gross total resection, while patients undergoing subtotal resection usually require radiotherapy. Complete resection without capsular violation can be curative and is often accomplished by simple resection of the filum above and below the tumor mass. Nevertheless, dissemination and distant treatment failure may occur in approximately 30% of the cases. In this paper, we propose an original MPE classification, which is based upon our personal series report concerned with tumor location and its correlation with the extent of resection. We also provide literature review, discussing surgical technique, tumor recurrence rate and dissemination, and adjuvant treatment. In conclusion, our findings suggest that MPE management based on the proposed 5-type tumor classification is favorable when total surgical resection is performed in carefully selected patients. Yet, further studies on a much broader model is obligatory to confirm this.