Nishio S, Morioka T, Fujii K, Inamura T, Fukui M
Department of Neurosurgery, Neurological Institute, Graduate School of Medicine, Kyushu University, Fukuoka, Japan.
J Clin Neurosci. 2000 Jan;7(1):20-3. doi: 10.1054/jocn.1999.0128.
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.
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。