...
首页> 外文期刊>Journal of clinical neuroscience: official journal of the Neurosurgical Society of Australasia >Clinicopathological and molecular features of malignant optic pathway glioma in an adult
【24h】

Clinicopathological and molecular features of malignant optic pathway glioma in an adult

机译:成人恶性视神经胶质瘤的临床病理和分子特征

获取原文
获取原文并翻译 | 示例
           

摘要

Malignant gliomas of the optic pathway are rare, and their genetic alterations are poorly understood. We describe a 64-year-old woman with anaplastic astrocytoma originating from the optic pathway, together with the molecular features. She presented with progressive visual field loss, and a biopsy sample was obtained from the lesion in the optic chiasm. She underwent radiosurgery concomitant with temozolomide chemotherapy, and subsequently remained stable for 10 months after initial presentation. Molecular analysis indicated that the mass may have shared common molecular genetic features with conventional primary astrocytic gliomas but not pilocytic gliomas, which supported the morphologic diagnosis of anaplastic astrocytoma. Molecular analysis of malignant optic pathway gliomas in adults is useful for distinguishing between high-grade gliomas and anaplastic pilocytic astrocytomas, and for determining further therapy. (C) 2014 Elsevier Ltd. All rights reserved.
机译:视神经通路的恶性神经胶质瘤很少见,其遗传改变知之甚少。我们描述了一名64岁的妇女,患有变性性星形细胞瘤,起源于视觉途径,以及分子特征。她表现为进行性视野丧失,并从视交叉的病变处获得了活检样本。她接受了替莫唑胺化学疗法的放射外科手术,随后在初次就诊后保持稳定10个月。分子分析表明,该肿块可能与常规原发性星形细胞胶质瘤具有共同的分子遗传学特征,而并非细胞性胶质细胞瘤,这支持间变性星形细胞瘤的形态学诊断。成人恶性视神经胶质瘤的分子分析可用于区分高级神经胶质瘤和间变性毛细胞星形细胞瘤,并用于确定进一步的治疗方法。 (C)2014 Elsevier Ltd.保留所有权利。

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