...
首页> 外文期刊>Acta Neuropathologica >Primary leptomeningeal oligodendroglioma with documented progression to anaplasia and t(1;19)(q10;p10) in a child.
【24h】

Primary leptomeningeal oligodendroglioma with documented progression to anaplasia and t(1;19)(q10;p10) in a child.

机译:儿童原发性脑膜神经少突胶质细胞瘤进展为发育不全和t(1; 19)(q10; p10)。

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

Oligodendrogliomas are infiltrating gliomas typically arising in the cerebral cortex and white matter. Rare examples present with diffuse leptomeningeal involvement in the absence of a clinically/radiologically detectable intra-parenchymal tumor [1-5, 7, 8, 10, 14, 15]. Although oligodendrogliomas are rare in children, most primary leptomeningeal oligodendrogliomas have occurred in the first decade of life (Table 1). We report the case of a 3-year-old girl, who presented with progressive regression of her ability to walk and an increase of cranial circumference.
机译:少突胶质细胞瘤是浸润性胶质瘤,通常发生在大脑皮层和白质中。在缺乏临床/放射学上可检测到的实质内肿瘤的情况下,罕见的例子是弥漫性软脑膜侵犯[1-5、7、8、10、14、15]。尽管少突胶质神经胶质瘤在儿童中很少见,但大多数原发性软脑膜少突胶质神经胶质瘤发生在生命的头十年(表1)。我们报告了一个3岁女孩的情况,该女孩的行走能力和颅周长的增加逐渐恶化。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号