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小脑星形细胞瘤。毛细胞型和弥漫性星形细胞瘤的比较临床病理研究。

Astrocytomas of the cerebellum. A comparative clinicopathologic study of pilocytic and diffuse astrocytomas.

作者信息

Hayostek C J, Shaw E G, Scheithauer B, O'Fallon J R, Weiland T L, Schomberg P J, Kelly P J, Hu T C

机构信息

Division of Radiation Oncology, Mayo Clinic, Rochester, Minnesota 55905.

出版信息

Cancer. 1993 Aug 1;72(3):856-69. doi: 10.1002/1097-0142(19930801)72:3<856::aid-cncr2820720335>3.0.co;2-k.

Abstract

BACKGROUND

The majority of patients with astrocytomas of the cerebellum have an excellent prognosis; however, a small percentage of patients continue to do poorly. To clarify the clinical, pathologic, and treatment characteristics that determine prognosis and therapeutic recommendations, a large group of patients with astrocytic tumors of the cerebellum was reviewed and analyzed.

METHODS

A clinicopathologic analysis was performed of all patients undergoing initial operation for astrocytomas in the cerebellum between 1960 and 1984. Of the 132 patients, 105 patients had pilocytic astrocytomas and 27 had diffuse astrocytomas.

RESULTS

Multivariate analysis revealed that the division of pilocytic and diffuse histologic type was the most significant prognostic factor influencing survival. The 5-year, 10-year, and 20-year survival rates were 85%, 81%, and 79%, respectively, for patients with pilocytic astrocytomas and 7%, 7%, and 7%, respectively, for patients with diffuse astrocytomas (P < 0.001). Pilocytic astrocytomas occurred in a younger age group and were more commonly cystic and completely resected.

CONCLUSIONS

Astrocytomas of the cerebellum can be divided into two principal groups, the pilocytic and the diffuse astrocytomas, each of which has distinct clinical, pathologic, and prognostic characteristics.

摘要

背景

大多数小脑星形细胞瘤患者预后良好;然而,一小部分患者预后仍然很差。为了阐明决定预后和治疗建议的临床、病理及治疗特征,我们对一大组小脑星形细胞瘤患者进行了回顾和分析。

方法

对1960年至1984年间所有因小脑星形细胞瘤接受初次手术的患者进行临床病理分析。132例患者中,105例为毛细胞型星形细胞瘤,27例为弥漫性星形细胞瘤。

结果

多因素分析显示,毛细胞型和弥漫性组织学类型的划分是影响生存的最显著预后因素。毛细胞型星形细胞瘤患者的5年、10年和20年生存率分别为85%、81%和79%,弥漫性星形细胞瘤患者分别为7%、7%和7%(P<0.001)。毛细胞型星形细胞瘤发生于较年轻的年龄组,更常见为囊性且可完全切除。

结论

小脑星形细胞瘤可分为两个主要类型,即毛细胞型和弥漫性星形细胞瘤,每一种都有独特的临床、病理和预后特征。

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