首页> 外文期刊>Child's nervous system: ChNS : official journal of the International Society for Pediatric Neurosurgery >Cranial and spinal oligodendrogliomatosis: a case report and review of the literature
【24h】

Cranial and spinal oligodendrogliomatosis: a case report and review of the literature

机译:颅和脊柱少突胶质瘤病:一例病例报告并文献复习

获取原文
获取原文并翻译 | 示例
           

摘要

Oligodendrogliomatosis is a rarely reported entity in literature associated with poor prognosis in terms of length and quality of life. In this paper, we describe oligodendrogliomatosis in a 15-year-old male who initially presented with altered mental status due to diabetic ketoacidosis.
机译:少突神经胶质瘤病是文献中很少报道的与寿命和生活质量预后不良相关的实体。在本文中,我们描述了一名15岁男性的少突胶质瘤病,该男性最初由于糖尿病性酮症酸中毒而出现精神状态改变。

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