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脊髓胶质瘤:参考辅助治疗的管理与预后

Spinal cord gliomas: management and outcome with reference to adjuvant therapy.

作者信息

Nishio S, Morioka T, Fujii K, Inamura T, Fukui M

机构信息

Department of Neurosurgery, Neurological Institute, Graduate School of Medicine, Kyushu University, Fukuoka, Japan.

出版信息

J Clin Neurosci. 2000 Jan;7(1):20-3. doi: 10.1054/jocn.1999.0128.

DOI:10.1054/jocn.1999.0128
PMID:10847645
Abstract

The authors review their experience with 19 consecutive cases with either astrocytic tumour (glioblastoma multiforme one, anaplastic astrocytoma one, astrocytoma 4, pilocytic astrocytoma 4) or ependymoma (10 tumours in 9 patients) of the spinal cord who were treated during the period from 1982 to 1996. The patients included 10 male and 9 female patients with a median age of 38 years. The main tumour locations included the cervicomedullary region 5 the cervical cord (8), the thoracic cord (5) and one each in the thoracolumbar region and conus medullaris. While a total removal of the tumour was achieved in 8 out of 10 ependymomas, the initial treatment for astrocytic tumours was a partial resection in 5, and biopsy in the remaining 5. As adjuvant treatment, 8 patients received radiation therapy and 2 received chemotherapy. Two patients with an astrocytic tumour received chemotherapy only, while the remaining 9 received neither radiation therapy nor chemotherapy initially. After these treatments, 6 out of the 8 patients with low grade astrocytoma have remained alive for 1.3-12.6 years, while 2 patients with high grade astrocytic tumours died within 15 months following surgery. Eight out of 9 patients with an ependymoma have remained alive for 3.0-12.3 years, while one committed suicide 2 years after surgery. As a result, 14 patients are still alive; half of them are accompanied by a mild neurological dysfunction, while the remaining one has a moderate deficit. The postoperative results and the rationale for surgery is discussed, and an approach for utilising adjuvant therapy for high grade tumours is also suggested.

摘要

作者回顾了1982年至1996年期间连续治疗的19例脊髓星形细胞瘤(多形性胶质母细胞瘤1例、间变性星形细胞瘤1例、星形细胞瘤4例、毛细胞型星形细胞瘤4例)或室管膜瘤(9例患者共10个肿瘤)的经验。患者包括10名男性和9名女性,中位年龄为38岁。主要肿瘤部位包括颈髓区域5例、颈段脊髓(8例)、胸段脊髓(5例),胸腰段区域和圆锥各1例。10例室管膜瘤中有8例实现了肿瘤全切,而星形细胞瘤的初始治疗中5例行部分切除术,其余5例行活检。作为辅助治疗,8例患者接受了放射治疗,2例接受了化疗。2例星形细胞瘤患者仅接受了化疗,其余9例最初既未接受放射治疗也未接受化疗。经过这些治疗,8例低级别星形细胞瘤患者中有6例存活了1.3至12.6年,而2例高级别星形细胞瘤患者在手术后15个月内死亡。9例室管膜瘤患者中有8例存活了3.0至12.3年,1例在手术后2年自杀。结果,14例患者仍存活;其中一半伴有轻度神经功能障碍,其余1例有中度功能缺陷。讨论了术后结果及手术的理论依据,并提出了对高级别肿瘤使用辅助治疗的方法。

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