Original Article
Author Details :
Volume : 3, Issue : 3, Year : 2016
Article Page : 470-478
Abstract
Introduction: Ependymomas are glial neoplasms that account for 4-8% of primary CNS neoplasms. Considerable controversy exists with regards to their prognosis and management, owing to their rarity and heterogeneity.
Objectives: To study the clinical and pathologic features of ependymomas and evaluate their important prognostic variables.
Materials and Methods: A 10 year retrospective study was carried out. The age, sex, location, clinical presentation, radiologic findings, microscopy, type of excision and follow up findings were studied.
Results: 168 ependymomas were identified in a total of 6628 biopsies((2.53%). Majority were seen in the second decade (42/168), M:F ratio was 2:1. 15.48% (26 cases) occurred in the supratentorial compartment, 36.92% (62 cases) infratentorially, and 47.61% (80 cases) in the spinal cord. 90% of the intracranial tumors presented with features of raised ICT while patients with spinal tumors had focal motor deficits. There were 146 classic grade II ependymomas(78.5%), most common location being the posterior fossa, 36 myxopapillary ependymomas(17.8%), all seen in the lumbosacral region and 6 anaplastic ependymomas(3.57%). Anaplastic ependymomas were seen supratentorially in children and young adults while the peak of myxopapillary tumours was in third and fourth decades. 105 patients underwent gross or near total excision while in 16 it was partial or subtotal.
Follow up was available in 73 patients. 9 patients died in the immediate post – operative period. Follow up for the rest varied from 3 months to 9 years. Anaplastic ependymomas were associated with a poorer prognosis. In supratentorial and lumbosacral tumours there was no difference in survival between gross total and subtotal excision while in adult infratentorial grade II ependymomas and cervical ependymomas, gross total excision had a better three year survival.
Conclusions: The prognosis of ependymomas is multifactorial and depends on histologic type and extent of surgical removal
How to cite : Shenoy A S, Kothari K S, Shaikh I, Phadke A, Goel N, Ependymomas: A clinicopathologic study. Indian J Pathol Oncol 2016;3(3):470-478
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