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OBJECTIVE: To explore inhibitory effects of the human amniotic mesenchyme stem cells on C6 glioma cells.
目的：探讨人羊膜间充质干细胞对C6胶质瘤细胞生长的抑制作用。
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18F-FDG PET is more sensitive and accurate than MRI in differentiating radionecrosis and recurrence of gliomas after interstitial brachytherapy.
18F-FDG PET在胶质瘤间质内放疗后区分放射性坏死与肿瘤复发方面较MRI更敏感而准确。
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Compared with the pathological examinations of the 21 cases, the accuracy of distinguishing recurrent tumor was 61.9% and 90.5% for mri and for pet respectively. conclusion 18f-fdg pet is more sensitive and accurate than mri in differentiating radionecrosis and recurrence of gliomas after interstitial brachytherapy.
18f-fdg pet在胶质瘤间质内放疗后区分放射性坏死与肿瘤复发方面较mri更敏感而准确。
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Postoperative pathological results revealed that 79 cases (86.8%) were low-grade gliomas, 4 cavernous hemangiomas, 4 anaplastic astrocytomas, 2 gliosis, 1 arteriovenous malformation, and 1 gliosarcoma.
术后病理结果示低级别胶质瘤79例(86.8%)，海绵状血管瘤4例，间变性星形细胞瘤4例，神经胶质增生2例，动静脉畸形1例，胶质肉瘤1例。
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Methods Animal models were established on BALB/c nude mice with subcutaneously transplanted neoplasma of U87 glioma.
建立BALB/c裸鼠U87胶质瘤移植瘤模型，将荷瘤裸鼠随机分为2组，采用间质内注射给药方法。
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Results: The findings on CT and MRI were as follows: 57 cases of Oligodendroglioma, 15 cases of Ganglioglioma , 5 cases of Dysembryoplastic neuroepithelial tumor , 3 cases of Pleomorphic xanthoastrocytoma .
结果：少枝胶质瘤47例，间变性少枝胶质瘤10例，节细胞胶质瘤15例，胚胎发育不良性神经上皮瘤5例，多形黄色细胞瘤3例。
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Results: the findings on ct and mri were as follows: 57 cases of oligodendroglioma, 15 cases of ganglioglioma , 5 cases of dysembryoplastic neuroepithelial tumor , 3 cases of pleomorphic xanthoastrocytoma .conclusion:the images on ct and mri of cerebra peripheral tumor occur some characters , so ct and mri were certain worth on the diagnose and differentiate diagnose of cerebra peripheral tumor.
结果：少枝胶质瘤47例，间变性少枝胶质瘤10例，节细胞胶质瘤15例，胚胎发育不良性神经上皮瘤5例，多形黄色细胞瘤3例。结论：脑浅表肿瘤存在影像特征，ct及mri对其诊断有一定的价值。少枝胶质细胞瘤；节细胞肿瘤；胚胎发育不良性神经上皮瘤；多形性黄色星形细胞瘤；ct；mri
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This is a retrospective analysis of 194 patients with primary malignant brain tumor, who registered between January 1, 1970 and December 31, 1979 in cancer registration, Cancer Therapy Center, Veterans General Hospital, Taipei, Taiwan, R.O.C. There were 36 cases of glioblastoma multiforme, 86 cases of malignant astrocytoma (grade Ⅲ and a few grade Ⅱ), 22 of medulloblastoma, 12 of oligodendroglioma, 11 of ependymoma or ependymoblastoma and 27 cases of other types. There were 141 male cases with ages ranging from ito 81 years with a mean of 33.3±19.3 and median of 34 years.
自1970年1月至1979年12月台北荣民总医院癌病治疗中心癌病登记组共登记了194例原发恶性脑瘤其中多形神经胶母细胞瘤有36例，第二级及第三级星细胞瘤有86例，神经管胚细胞瘤有22例，间胶质母细胞瘤有12例，室管膜瘤或室管膜胚细胞瘤(ependy-moblastoma)有11例，其他有27例。
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About 48%(90/194) were below 29 years of age. Ninety-nine of 194 cases had either radiotherapy alone or supplementary treatment with radiotherapy following surgery. We analyzed multiple prognostic factors. The factors of importance included postoperative radiotherapy; female in glioblastoma multiforme; the primary tumor dose above 5000 rads and/or whole brain irradiation in malignant astrocytoma and glioblastoma multiforme; the primary tumor dose above 4500 rads in ependymoma, medulloblastoma and oligodendroglioma; and spinal axis irradiation above 2000 rads in ependymoma and medulloblastoma that produced a better prognosis than in other groups.
男与女之比例为2.7比1，年龄分布自1至81岁，平均年龄33.3±19.3岁，中值年龄为34岁，29岁以下占48%(90/194)，其中99例单独或手术后辅以放射腺治疗，分析同种脑瘤的预后因素，其中多形神经胶母细胞瘤有手术后放射线治疗或女性，多形神经胶母细胞瘤合并星细胞瘤原发肿瘤剂量5000雷得以上或曾全颅腔照射，神经管胚细胞瘤，间胶质母细胞瘤，及室管膜瘤原发肿瘤剂量4500雷得以上，室管膜瘤及神经管胚细胞瘤有脊轴照射2000雷得以上预后均佳，且统计上有显著的差异。
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Methods:Thirty-seven glioma specimens were classified as astrocytoma(25 cases, including 7 fibrillary cases; 6 protoplasmic cases; 12 anaplasfic cases), and glioblastoma( 12 cases,including 4 GBM cases).
37例人脑胶质瘤标本按WHO分类标准(1990)分为：星形细胞瘤(25例，纤维型7例，原浆型6例，间变型12例)，胶质母细胞瘤(12例，包括GBM4例)。
- 更多网络解释与间胶质瘤相关的网络解释 [注：此内容来源于网络，仅供参考]
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Anaplastic oligodendroglioma：(间变性少突胶质细胞瘤)
Oligodendroglioma (少突胶质细胞瘤) | Anaplastic oligodendroglioma (间变性少突胶质细胞瘤) | Oligoastrocytic tumours少突星形细胞肿瘤
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Anaplastic astrocytoma：(间变性星形细胞瘤)
Protoplasmic astrocytoma (原浆性星形细胞瘤) | Anaplastic astrocytoma (间变性星形细胞瘤) | Glioblastoma (胶质母细胞瘤)