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原浆性星形细胞瘤中的MIB1和p53免疫反应性

MIB1 and p53 immunoreactivity in protoplasmic astrocytomas.

作者信息

Prayson R A, Estes M L

机构信息

Department of Anatomic Pathology, Cleveland Clinic Foundation, Ohio 44195, USA.

出版信息

Pathol Int. 1996 Nov;46(11):862-6. doi: 10.1111/j.1440-1827.1996.tb03559.x.

Abstract

Pure protoplasmic astrocytomas are a group of rarely encountered low grade astrocytic neoplasms. Relatively few studies have specifically examined this subset of tumors. A series of 18 protoplasmic astrocytomas in 14 males and four females (age range 2.5-52, mean 22 years) were studied in order to examine MIB1 (a marker of cell proliferation) and p53 (a tumor suppressor gene) immunoreactivity. All patients presented with seizures (mean duration 94 months) and three with headaches also. Eight tumors were located in the temporal lobe and six in the frontal lobe. All tumors were characterized by a proliferation of astrocytes with round nuclear contours arranged against a microcystic background. Only rare foci of mild vascular proliferation (3 tumors), rare mitotic figures (1 tumor), and mild nuclear atypia (3 tumors) were observed. Most tumors were primarily cortical in location. Necrosis was not seen in any of the tumors. MIB1 indices (number of MIB1 positive tumor cells/1000 tumor cells evaluated x 100) ranged from 0 to 4.3 (mean 0.7); in five tumors, no MIB1 staining was observed. p53 immunoreactivity was noted in 5 of 18 tumors (28%). Five patients received adjuvant radiation therapy and one adjuvant chemotherapy. At last known follow-up, 11 patients are alive with no evidence of residual tumor (mean 70 months), six patients are alive with evidence of residual tumor (mean 58 months), and one patient died of complications unrelated to the tumor (36 months) postoperatively. Based on these findings, the conclusions presented are as follows: (i) MIB1 indices are generally low in these tumors, corroborating the clinical impression of a slow growing neoplasm; and (ii) p53 immunoreactivity is observed in a minority of protoplasmic astrocytomas.

摘要

纯原浆性星形细胞瘤是一组罕见的低级别星形细胞肿瘤。相对较少的研究专门针对这一肿瘤亚型进行过检查。我们对14名男性和4名女性(年龄范围2.5 - 52岁,平均22岁)的18例原浆性星形细胞瘤进行了研究,以检测MIB1(一种细胞增殖标志物)和p53(一种肿瘤抑制基因)的免疫反应性。所有患者均有癫痫发作(平均病程94个月),3例还伴有头痛。8个肿瘤位于颞叶,6个位于额叶。所有肿瘤的特征均为星形细胞在微囊性背景下呈圆形核轮廓增殖。仅观察到罕见的轻度血管增生灶(3个肿瘤)、罕见的核分裂象(1个肿瘤)和轻度核异型性(3个肿瘤)。大多数肿瘤主要位于皮质。所有肿瘤均未见到坏死。MIB1指数(MIB1阳性肿瘤细胞数/评估的1000个肿瘤细胞×100)范围为0至4.3(平均0.7);5个肿瘤未观察到MIB1染色。18个肿瘤中有5个(28%)观察到p53免疫反应性。5例患者接受了辅助放疗,1例接受了辅助化疗。在最后一次已知随访时,11例患者存活且无残留肿瘤证据(平均70个月),6例患者存活但有残留肿瘤证据(平均58个月),1例患者术后死于与肿瘤无关的并发症(36个月)。基于这些发现,得出如下结论:(i)这些肿瘤的MIB1指数通常较低,证实了肿瘤生长缓慢的临床印象;(ii)少数原浆性星形细胞瘤观察到p53免疫反应性。

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