首页> 美国卫生研究院文献>The Medical Bulletin of Sisli Etfal Hospital >A Rare Tumor in Childhood Desmoplastic Infantile Astrocytoma: Two Case Reports
【2h】

A Rare Tumor in Childhood Desmoplastic Infantile Astrocytoma: Two Case Reports

机译:儿童少增生性小儿星形细胞瘤罕见肿瘤:两例报道

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。
获取外文期刊封面目录资料

摘要

Desmoplastic infantile astrocytomas (DIAs), are rare supratentorial tumors, usually observed in the first 24 months of life. Despite their aggressive appearance, they tend to follow a favorable clinical course. Total or near total resection of tumor is usually the treatment option. Desmoplastic Infantile Ganglioglioma (DIG) and DIA are WHO grade I tumors that have similar clinical and morphological findings. The only criterion in differential diagnosis is the neural component of DIG. These tumors both have dense fibroblastic stroma and positive staining with glial fibrillar acidic protein (GFAP) and CD34.
机译:增生性婴儿星形细胞瘤(DIAs)是罕见的幕上肿瘤,通常在生命的头24个月内观察到。尽管它们具有侵略性的外观,但它们倾向于遵循良好的临床过程。通常选择肿瘤全切除或近全切除。增生性小儿神经节神经胶质瘤(DIG)和DIA是WHO的I级肿瘤,具有相似的临床和形态学发现。鉴别诊断的唯一标准是DIG的神经成分。这些肿瘤都具有致密的成纤维细胞基质,并具有胶质纤维酸性蛋白(GFAP)和CD34阳性染色。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

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