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Holocord oligodendroglioma with intracranial extension in a young adult: a case report and review of literature

机译:青年成人颅内胆管少突胶质瘤的病例报道及文献复习

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摘要

Widespread primary spinal oligodendrogliomas are a rare variety of tumors that usually affect children. Currently, there are only two adult cases reported worldwide. We report the first case of primary holocord oligodendroglioma with intracranial extension in a young adult female. The patient presented with a 4-month history of fluctuating hemiparesis of the left upper extremity eventually becoming quadriplegic after 1 month. Imaging findings revealed a contrast-enhancing holocord neoplasm spanning from the cervical region to the conus medullaris and with extension to the lower medulla. The patient succumbed to severe pneumonia after 1 month of admission. An autopsy was done and the histopathologic findings were consistent with oligodendroglioma.
机译:广泛的原发性脊柱少突神经胶质瘤是一种罕见的肿瘤,通常会影响儿童。目前,全世界仅报告了两个成年病例。我们报告了第一例年轻成人成年女性伴颅内扩张的原发性全胆少突胶质瘤。该患者有4个月的左上肢偏瘫波动波动史,最终在1个月后变为四肢瘫痪。影像学检查结果显示,对比度增强的全恶性肿瘤从宫颈区域延伸至延髓圆锥,并延伸至下延髓。入院1个月后患者死于严重的肺炎。进行了尸检,组织病理学结果与少突胶质细胞瘤一致。

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