...
首页> 外文期刊>Journal of neuro-oncology. >Primary anaplastic pleomorphic xanthoastrocytoma with widespread neuroaxis dissemination at diagnosis--a pediatric case report and review of the literature.
【24h】

Primary anaplastic pleomorphic xanthoastrocytoma with widespread neuroaxis dissemination at diagnosis--a pediatric case report and review of the literature.

机译:原发性间变性多形性黄体星形细胞瘤在诊断时具有广泛的神经轴传播-儿科病例报告并文献复习。

获取原文
获取原文并翻译 | 示例

摘要

We report a 5 year-old boy with primary anaplastic pleomorphic xanthoastrocytoma (PXA) with whole neuroaxis dissemination at diagnosis who experienced the sudden onset of generalized convulsion. Head- and spinal magnetic resonance imaging (MRI) showed widespread gadolinium (Gd)-enhanced lesions extending to the bilateral frontal- and medial temporal lobes and the spinal cord. Subsequent MRI study demonstrated that the lesion size increased without any neurological deterioration. Under a histopathologic diagnosis of anaplastic PXA he underwent adjuvant chemotherapy consisting of 12 cycles of carboplatin and vincristine. The patient is alive without any neurological deficits; follow-up MRI showed that the lesions remained stable during 18 months of chemotherapy. We report a very rare pediatric case of primary anaplastic PXA with dissemination involving the entire neuroaxis at the time of diagnosis.
机译:我们报告了一个5岁男孩,在诊断时原发性间变性多形性星形胶质细胞瘤(PXA)伴有整个神经轴弥散,经历了突然的全身性惊厥发作。头颅和脊髓磁共振成像(MRI)显示广泛的g增强(Gd)增强的病变,延伸至双侧额叶和内侧颞叶和脊髓。随后的MRI研究表明,病变的大小增加了,而没有任何神经系统的恶化。在间变性PXA的组织病理学诊断下,他接受了辅助化疗,包括12个周期的卡铂和长春新碱。患者还活着,没有任何神经系统缺陷;后续的MRI显示,病变在化疗的18个月中保持稳定。我们报告了在诊断时极少见的原发性间变性PXA儿科病例,其传播涉及整个神经轴。

著录项

相似文献

  • 外文文献
  • 中文文献
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