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脑干胶质瘤:23例组织学确诊病例的临床病理分析

Brain stem gliomas: a clinicopathological analysis of 23 histologically proven cases.

作者信息

Nishio S, Fukui M, Tateishi J

机构信息

Department of Neurosurgery, Faculty of Medicine, Kyushu University, Fukuoka, Japan.

出版信息

J Neurooncol. 1988 Nov;6(3):245-50. doi: 10.1007/BF00163708.

Abstract

The clinical and anatomic pathological findings in 23 patients with histologically proven brain stem glioma were reviewed. Eleven patients had malignant tumors (astrocytoma, grade III, and glioblastoma multiforme) and the remaining had low grade ones. The primary site of the tumor was the pons in 15 of 21 patients examined, followed by the medulla oblongata and midbrain. Continuous cephalad and caudad involvement of pontine tumors was evident in 14 patients, and was more extensive in the high grade gliomas. At autopsy, the tumor spread via the CSF was observed in all patients with high grade but not low grade tumors. Open surgical posterior fossa exploration was performed on 12 patients. Volume reduction, by partial removal of the tumor and/or by cyst evacuation, was performed on seven, with good results. Nineteen patients were given radiation therapy, with temporary improvement of the clinical conditions. While none of the patients with malignant tumors survived more than 15 months after diagnosis, those with low grade tumors had a five-year actuarial survival rate of 50.0%, and three survived more than ten years after the diagnosis. Our data indicate that brain stem gliomas are not a homogeneous group of tumors as far as the clinical and pathological features are concerned. This heterogeneity shows the need to design specific treatments for these tumors.

摘要

对23例经组织学证实的脑干胶质瘤患者的临床及解剖病理学发现进行了回顾。11例患者患有恶性肿瘤(星形细胞瘤,Ⅲ级,以及多形性胶质母细胞瘤),其余患者患有低级别肿瘤。在接受检查的21例患者中,15例肿瘤的原发部位在脑桥,其次是延髓和中脑。14例患者的脑桥肿瘤明显向头侧和尾侧连续蔓延,在高级别胶质瘤中更为广泛。尸检时,在所有高级别肿瘤患者而非低级别肿瘤患者中观察到肿瘤通过脑脊液扩散。对12例患者进行了后颅窝开放手术探查。7例患者通过部分切除肿瘤和/或排空囊肿进行了减容,效果良好。19例患者接受了放射治疗,临床状况有暂时改善。虽然恶性肿瘤患者在诊断后均未存活超过15个月,但低级别肿瘤患者的5年精算生存率为50.0%,3例患者在诊断后存活超过10年。我们的数据表明,就临床和病理特征而言,脑干胶质瘤并非一组同质的肿瘤。这种异质性表明需要针对这些肿瘤设计特定的治疗方法。

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