منابع مشابه
Giant Cell Ependymoma of The Filum Terminale: A Case Report
Ependymomas accounts for about 2%–6% of CNS and 60%–70% of spinal cord tumors. Several histological patterns of these neoplasms are well known, but little attention has been devoted to a variant composed of giant cells. In spite of apparently “worrisome” histology, giant cell ependymoma seems to be a neoplasm with a relatively good prognosis. This report presents a case of giant cell ependym...
متن کاملClear Cell Ependymoma of Spinal Cord: A Case Report
Clear cell variant of ependymoma is almost exclusively located in the supratentorial region. Only few cases of this tumor that located in the spinal cord have been reported. Here we report one case of intramedullary clear cell ependymoma of the lumbar spinal cord. In microscopic examination, the tumor cells were round to oval with moderate amounts of clear cytoplasm and centrally located lar...
متن کاملSacrococcygeal extraspinal ependymoma: a case report.
Ependymomas, the common glial tumors of the spinal cord, occur occasionally outside the central nervous system and are called extraspinal ependymomas (ESE). ESE, which are clinically confused with other sacrococcygeal tumors, are rarely seen and found primarily in the sacrococcygeal region during childhood. We report a case of a seven-year-old boy presenting with a midline mass (6 cm diameter) ...
متن کاملPituitary Glioblastoma: A Case Report
INTRODUCTION Pituitary adenomas have been the most common sellaturcica tumors. There have been many unusual types of pituitary tumors that might neglect by radiologists and clinicians. One of these tumors would be the malignant glioma. CASE PRESENTATION A 62-year-old male has complained from sudden frontal headache, nausea, vomiting, decreased vision, blurred vision and double vision. In skul...
متن کاملA novel case of quartet tumor: meningioma, angiomyolipoma, ependymoma and sarcoma: report of a case and review of the literature
Multiple primary tumors in a single patient are relatively rare when four or more distinct lesions are considered. Herein, we report a case of woman with four different primary tumors: meningioma, renal angiomyolipoma, spinal ependymoma and high-grade soft tissue sarcoma. There was no family history and hereditary syndrome. The genetic analysis was completely normal. To best of our knowledge, t...
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ژورنال
عنوان ژورنال: Neuro-Oncology Advances
سال: 2019
ISSN: 2632-2498
DOI: 10.1093/noajnl/vdz039.181