Characterization of a Clival Chordoma Xenograft Model Reveals Tumor Genomic Instability

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Establishment and characterization of a primary human chordoma xenograft model.

OBJECT Chordomas are rare tumors arising from remnants of the notochord. Because of the challenges in achieving a complete resection, the radioresistant nature of these tumors, and the lack of effective chemotherapeutics, the median survival for patients with chordomas is approximately 6 years. Reproducible preclinical model systems that closely mimic the original patient's tumor are essential ...

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Intradural Clival Chordoma: A Case Report

Clival chordoma is a rare intracranial neoplasm located in the clivus with bony extension and destruction. It is difficult to resect completely and generally has a poor prognosis. However, intradural clival chordomas have been reported with good surgical outcomes. We present a rare case of intradural chordoma and a review of the literature.

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Delayed intraventricular metastasis of clival chordoma

Intracranial chordomas are typically clival and extradural in location, yet these tumors can obviously invade the dura. However, primary intradural chordomas without local extension is a rare event with approximately 47 cases reported in literature. Furthermore, all intradural chordoma reports appear to be extraventricular in location.[1,2] In addition, through advances in technology and optics...

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ژورنال

عنوان ژورنال: The American Journal of Pathology

سال: 2018

ISSN: 0002-9440

DOI: 10.1016/j.ajpath.2018.08.004