Brain magnetic resonance (MR) revealed a 1.5×1.5 cm diffuse enhancing mass in the right postcentral gyrus cortex with some focal calcifications. magnetic resonance imaging (MRI) revealed hyperintensity on T1-weighted images and mixed hypo-to hypertensity on T2-weighted images. The mass had relatively smooth margins and only minimal brain swelling was noted around the peri-mass lesion. On the sagittal image the mass was closely contacted with dura of the sagittal sinus and falx. There was low signal line between the mass and dura, showing the presence of cerebro-spinal fluid. Imaging showed no evidence that the mass was connected to the ventricular ependymal lining (Fig. 1).The neuro-radiologic differential diagnosis included dysembryoplastic neuroepithelial tumor or low grade glioma, and meningioma less likely, due to the parasagittal tumor location.
Operation and pathological findingsA right parietal craniotomy was performed and complete excision of the tumor was done. The tumor was firm, gray, and contained calcifications. It had well defined margins, allowing
INTRODUCTIONEpendymomas are rare neuroectodermal tumors arising from ependymal cells of the ventricular system, choroid plexus, filum terminale, or central canal of the spinal cord. Ependymomas are relatively rare nervous system tumors, constituting 1.2% to 7.8% of all intracranial neoplasms or 2% to 6% of all gliomas 4,9) . Ependymomas are frequently infratentorial, and a third of ependymomas are supratentorial. Supratentorial ependymomas outside the ventricular system as a distinct location are infrequent. As reported in some articles, ectopic ependymoma can arise in the supratentorial parenchyma with no attachment to the ventricular system 3) . However, these are very rare and reported in only a few cases in the literature 9) . Our patient was only 21 months old, which to our knowledge, is the youngest pediatric case of supratentorial ectopic cortical ependymoma in published papers. Herein, the clinical features and pathologic findings of supratentorial ectopic cortical ependymoma in are described.
CASE REPORT
History and examinationA 21-month-old boy presented with repetitive left leg rigidity lasting two weeks. At birth he was delivered vaginally without J Korean Neurosurg Soc 50 : 244-247, 2011 http://dx.doi.org/10. 3340/jkns.2011.50.3.244 Copyright © 2011 The Korean Neurosurgical Society Two-thirds of ependymomas arise in the infratentorial or intraventricles, whereas one-third are located supratentorially. But supratentorial "cortical" ependymomas are very rare. We report a case of a cortical ependymoma in a 21-month-old boy. The patient presented with simple partial seizures. This tumor was located in the postcentral gyrus and he had gross total excision. Microscopy and immunohistochemistry showed grade II differentiation ependymoma.