Journal of Neurosciences in Rural Practice
 
CASE SERIES
Year : 2019  |  Volume : 10  |  Issue : 2  |  Page : 316-320

Spinal cord ependymoma – Surgical management and outcome


1 Department of Neurosurgery, Beaumont Hospital, Dublin, Ireland
2 Department of Neuropathology, Beaumont Hospital, Dublin, Ireland

Correspondence Address:
Wail Mohammed
Department of Neurosurgery, Cork University Hospital, Wilton, Cork
Ireland
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/jnrp.jnrp_267_18

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Background: Ependymoma is a common primary neoplasm of the spinal cord and filum terminale. Patients with spinal ependymoma usually experience gradual symptoms due to slow progression of the tumor; thus, early diagnosis can be challenging to make. Objective: The objective of this study was to report 5 years' experience in treating spinal intramedullary ependymomas and to illustrate the advantage of aggressive complete resection whenever possible. Patients and Methods: Retrospective medical notes of all patients with spinal ependymoma treated surgically over a 5-year period between January 2003 and January 2008 were recorded. Clinical presentation, spinal level, extent of resection, and complications were recorded. A prolonged follow-up was documented. Results: There were 20 patients – 11 males, and nine females –included in this study. Their median age was 48 years (range 3–75 years). In 18 patients, total gross resection was achieved. Subtotal resection was only possible in one patient due to surgical difficulty. One patient underwent biopsy and referred for further surgery and subsequently had total resection. Conclusions: Radical total resection is achievable in spinal ependymomas, with minimal resultant morbidity.


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