它由星形细胞瘤，少突胶质细胞瘤，室管膜瘤发展而来，它们是由神经外胚层细胞诱导的。
It developed from astrocytoma, oligodendroglioma, ependymoma, which were induced by neural ectoblast.
局部有相对一致的细胞伴有核周空晕，让人考虑可能有少突胶质细胞瘤的成份。
Focally there are relatively uniform cells with perinuclear halos, raising the possibility of an oligodendroglioma component.
组织学上常常和少突胶质细胞瘤混淆，脑室内的中枢神经细胞瘤比脑实质内预后更好。
Histologically often confused with oligodendroglioma and has a better prognosis than the variety that involves the brain parenchyma.
星形细胞瘤、少突胶质细胞瘤、混合性胶质瘤全切除后预后良好，不需要进行辅助性治疗。
It is not necessary to perform auxiliary therapy for astrocytoma, oligodendroglioma, and mixed glioma, because the prognosis is good after total removal of the tumor.
结果间变性星形细胞瘤7例，多形性胶质母细胞瘤3例，少突胶质瘤1例，低级别胶质瘤1例。
Results There were 7 cases with anaplastic astrocytoma, 3 cases with glioblastoma multiforme, 1 cases with oligodendroglioma, 1 cases with lower grade glioma.
方法：应用免疫组织化学方法检测28例少突胶质细胞肿瘤、9例星形细胞瘤的OLIG2和GFAP表达情况。
Methods:Expressiof OLIG2 and GFAP in 28 oligodendrogliomas and 9 astrocytoma were measured by immunohistochemistry method.
方法：应用免疫组织化学方法检测28例少突胶质细胞肿瘤、9例星形细胞瘤的OLIG2和GFAP表达情况。
Methods:Expressiof OLIG2 and GFAP in 28 oligodendrogliomas and 9 astrocytoma were measured by immunohistochemistry method.
应用推荐