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首页> 外文期刊>Journal of neurological surgery reports. >Primary Spinal Glioblastoma Multiforme with Secondary Manifestation as a Cerebral “Angioglioma.” Literature Review and Case Report
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Primary Spinal Glioblastoma Multiforme with Secondary Manifestation as a Cerebral “Angioglioma.” Literature Review and Case Report

机译:原发性脊柱胶质母细胞瘤多发性表现为脑“血管神经胶质瘤”。文献综述和病例报告

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Primary intramedullary spinal glioblastoma multiforme (sGBM) with a secondary cerebral manifestation is a very rare entity with a poor outcome. Case studies show a mean average of survival of 10 months after diagnosis. These tumors tend to develop at a young age. A combination with an arteriovenous malformation in the same location has never been published before. Vascular malformations in association with cerebral glioblastomas have only been reported in five cases so far. Proangiogenic factors are assumed to be involved in the appearance of both entities. We present a case study and a review of the literature.
机译:具有继发性脑部表现的多发性原发性髓内脊髓胶质母细胞瘤(sGBM)是非常罕见的实体,其预后较差。案例研究显示,诊断后平均存活10个月。这些肿瘤倾向于在年轻时发展。以前从未公开过在同一位置合并动静脉畸形的组合。迄今为止,仅五例报道了与脑胶质母细胞瘤相关的血管畸形。促血管生成因子被认为与两个实体的外观有关。我们提出一个案例研究和文献综述。

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