Expression alterations define unique molecular characteristics of spinal ependymomas

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Expression alterations define unique molecular characteristics of spinal ependymomas

Ependymomas are glial tumors that originate in either intracranial or spinal regions. Although tumors from different regions are histologically similar, they are biologically distinct. We therefore sought to identify molecular characteristics of spinal ependymomas (SEPN) in order to better understand the disease biology of these tumors. Using gene expression profiles of 256 tumor samples, we id...

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Molecular alterations in ependymomas.

Ependymal tumours are uncommon neoplasms of the central nervous system. Basic molecular alterations underlying their development are not so well defined in contrast to the astrocytic tumours. We compiled literature data on the molecular changes in ependymomas to show clinical and pathological correlations and review the prognostic factors that may much better predict their clinical behaviour.

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Unusual paediatric spinal myxopapillary ependymomas: Unique molecular entities or pathological variations on a theme?

Ependymomas are the commonest type of spinal glioma which represent a group of relatively benign tumours. Myxopapillary ependymoma (MPE) is a common variant found within the distal spinal cord around the conus. These two entities are clearly differentiated on the basis of their characteristic histological and molecular features. Rare variants of MPE's are described in the literature to have the...

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Surgical management of intramedullary spinal ependymomas.

BACKGROUND Spinal intramedullary ependymoma is a rare disease with a wide range of clinical presentation, generally requiring surgical treatment. OBJECTIVE Report our experience and present our surgical technique to achieve total resection and cure. METHOD We present 12 consecutive cases of intramedullary ependymomas operated between 2000 and 2008 by the senior author (HT). The functional s...

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ژورنال

عنوان ژورنال: Oncotarget

سال: 2015

ISSN: 1949-2553

DOI: 10.18632/oncotarget.3715