摘要
目的探讨胶质肉瘤的流行病学特点,及其发病机制、治疗、预后和放射与继发胶质肉瘤之间的关系。方法手术治疗8例胶质肉瘤,并结合文献进行分析。结果全部镜下手术切除,肿瘤全切5例,次全切3例。随访中7例发现肿瘤复发,2例出现颅内转移,6例因肿瘤复发在术后2年内死亡。8例中2例为继发性,均在原发肿瘤术后接受过放疗。结论胶质肉瘤是罕见的高度恶性肿瘤,其复发、转移率高,预后不良,尽可能完全切除肿瘤是首选治疗方案,对复发肿瘤再次手术为延长生存时间的最佳手段。放射治疗与继发胶质肉瘤之间可能存在着一定的因果关系。
Objective To discuss the epidemiological and clinical features of the gliosareoma and to explore its pathogenesis, treatment, prognosis and the relationship between radiotherapy and secondary gliosarcoma. Methods To report 8 cases of gliosareoma which was operated under microscope and do analysis by reviewing literatures. Results Total removal was achieved in 5 cases, and subtotal in 3 cases. Of all were followed up, tumor recurrence was found in 7 cases( 87.5% ) , intracranial metastasis was found in 2 cases(25% ), and 6 cases died due to recurrent gliosarcoma in 2 years after operation. 2 out of 8 were secondary gliosareoma, both received radiotherapy after operation of the primary tumors. Conclusion Gliosareoma which is a kind of rare malignant tumor, has high recurrent, metastatic rate and bad prognosis. To remove the tumor as completely as possible is the first therapeutic regimen, and re-operation is the best method to prolong the survival time when gliosarcoma recurs and general condition permits. Moreover, there may exist a cause and effect relationship between radiotherapy and the secondary gliosareoma.
出处
《中华神经外科杂志》
CSCD
北大核心
2008年第4期243-245,共3页
Chinese Journal of Neurosurgery