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Six weeks after drug intervention,we found,in ADM+Res group,the mean tumor volume of MCF-7/ADM cells implanted tumor was 1.203±0.338 cm~3 with statistical significance to compare with other groups(P<0.05),decreased about 50.58%compared with the mean tumor volume of ADM alone group1.979±0.307 cm~3the result of the mean tumor weigh was alike to the mean tumor volume; compared with the control,Res could relieve weigh loss(P<0.05,and the toxicity of treatment was not obvious;Microscopic examination showed that there was massive area of cytoclasis and apoptosis in the tumor tissue of the combination group comparing with other groups.

实验结果提示用药6W后,ADM+Res组移植体积(1.203±0.338)cm~3明显小于其余各组,抑率为50.58%,与单用ADM组(1.979±0.307)cm~3相比有差异P<0.05肿重量的结果与体结果类似;未观察到用药后的毒副作用;经不同处理后,单独注射Res组小鼠体重较生理盐水组及ADM组有所增加(P<0.05,而ADM+Res组治疗前后体重无差异P>0.05HE结果显示与其他组相比,ADM+Res组肿组织中出现大片坏死区域。

Results In 316 patients including 97 cases of type Ⅰ(97 cases account for 30.7%) and 71 cases of type Ⅳ(71 cases account for 22.5%) by ultrasound;74 cases of Serous cystadenoma(74 cases account for 23.4%),58 cases of mucinous cystadenoma(58 cases account for 18.4%) and 56 cases of dermoid tumor56 c...

结果本组316例患者中卵巢肿超声分型以Ⅰ型居多(97例,占30.7%),其次为Ⅳ型(71例,占22.5%);病理分型以浆液性囊腺居多(74例,占23.4%),其次为黏液性囊腺(58例,占18.4)和畸胎(56例,占17.7%)。

Methods: We conducted a retrospective study of 100 patients surgically treated from 1964 to 1997, including 53 cases of abdominal wall desmoid tumor and 47 cases of extra-abdominal desmoid tumor.

回顾分析我院1964~1997年间外科收治的100例硬纤维,包括腹壁硬纤维53例,腹壁外硬纤维47例。

Gardner's syndrome, a hereditary syndrome of intestinal polyposis and colon cancer, has many cutaneous manifestations, including fibromas, epidermoid cysts (appearing before puberty, and not in acne-prone areas), osteomas, and desmoid tumors.

加德纳综合征是一种遗传性肠息肉、结肠综合征,有多种皮肤表现,如纤维、表皮样囊肿(发生于青春期之前,不发生于痤疮好发部位)、骨、纤维样等。

Gardner's syndrome, a hereditary syndrome of intestinal polyposis and colon cancer, has many cutaneous manifestations, including fibromas, epidermoid cysts (appearing before puberty, and not in acne-prone areas), osteomas, and desmoid tumors.

加德纳综合征是一种遗传性肠息肉、结肠癌综合征,有多种皮肤表现,如纤维、表皮样囊肿(发生于青春期之前,不发生于痤疮好发部位)、骨、纤维样等。

The time of cornea diabrosis, metastases into cervical lymph nodes and lung, survival time and ratio of CD4+ and CD8+ T cells in peripheral blood were observed.RESULTS: The time of cornea diabrosis in GTVC group or GTV group was later than that in PBS group, but no statistical difference between GTVC group and GTV group. Metastatic incidence in cervical lymph nodes of GTVC group mice or GTV group mice was lower than that in PBS group 18 days after the model had been established. There was no statistical difference in metastatic incidence between GTV group and GTVC group.

将荷模型鼠分为磷酸盐缓冲液(phosphatebuffered saline,PBS)治疗组,IL12基因修饰肿细胞疫苗(gene modified tumor cell vaccine, GTV)治疗组及GTV 联合CpGODN治疗组;鼠荷模型建立后的第3d及第10d分别在各组鼠结膜下注射30μL PBS,30μL(3.0×106个细胞)灭活的GTV及含20μg CpGODN灭活的GTV,进行角膜溃破时间、淋巴结和肺部转移发生率、生存时间及外周血CD4+和CD8+T细胞比例的观测。

I don't think this is a case of ependymoma or subependymoma or oligodendroglioma.

不考虑室管膜、室管膜下或少突胶质细胞

Results Of 80 cases 46 were acoustic neuromas (57.5%), 15 meningiomas (18.5%), 6 epidermoid cysts(7.5%), 5 trigeminal neuromas (6.3%) and 8 other rare tumors(10%).

结果 80例肿中,听神经46例(57.5%),脑膜15例(18.8%),上皮样囊肿6例(7.5%),三叉神经5例(6.3%)及其它少见肿8例(10%)。

Results (1)Most neoplasms in fourth ventricle had characteristic MRI appearances,such as meningioma,medulloblastoma,epidermoid cyst.

结果 (1)不同的中颅窝肿各具不同MR特征性表现,如三叉神经鞘、脑膜、骨母细胞等。

Week. Conclusions The S1 area brain glioma model established by this method in rats had the same characters as human brain glioma. The tumor growth period was short and the subsisting period was stable without extracerebral metastasis and extracranial extension. This model is suitable for laboratory and treatment study of brain gliomas.

该方法建立的S1区脑胶质模型具备与人脑胶质生长相似的特性,肿形成时间短,生存期稳定,且无脑外转移和颅外扩散,适合各种脑胶质实验治疗研究。

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