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成人脊髓髓内星形细胞瘤:术后结果

Intramedullary spinal cord astrocytoma in adults: postoperative outcome.

作者信息

Kim M S, Chung C K, Choe G, Kim I H, Kim H J

机构信息

Department of Neurosurgery, Seoul National University College of Medicine, South Korea.

出版信息

J Neurooncol. 2001 Mar;52(1):85-94. doi: 10.1023/a:1010680924975.

Abstract

Intramedullary spinal cord astrocytomas are relatively rare and usually low-grade lesions with a long natural history. The rarity of the condition and its indolent clinical course has made the evaluation of treatment efficacy difficult. To clarify postoperative outcome and prognostic factors, we performed a retrospective analysis of intramedullary spinal cord astrocytomas in a single institute. Twenty-eight patients were surgically treated between 1978 and 1999; of median age 36 years (range, 19-68 years); nineteen patients were males and nine females. All patients presented with pain and neurological deficits. The cervical cord was involved in fifteen patients, cervico-thoracic in five, thoracic in six and thoraco-lumbar in two. Gross total removal was performed in three patients, subtotal removal in six, partial removal in fourteen and biopsy only in five. Nineteen patients received radiation therapy postoperatively. The mean follow-up period was 31.9 months (range, 0.5-184 months). Low-grade astrocytomas were found in 18 cases, anaplastic astrocytoma in three cases and glioblastomas in seven cases. The median survivals of patients with low- and high-grade astrocytoma were 184 months and 8 months, respectively (p < 0.05). The median survivals of irradiated and non-irradiated patients with low-grade astrocytoma were 184 months and 102 months. Neither the extent of resection, nor radiation influenced the survival rate. In summary, the histological grade was the most significant predictor of survival in patients with astrocytoma of the spinal cord.

摘要

脊髓髓内星形细胞瘤相对少见,通常为低级别病变,自然病程较长。该病的罕见性及其缓慢的临床病程使得评估治疗效果变得困难。为了阐明术后结果和预后因素,我们对单一机构的脊髓髓内星形细胞瘤进行了回顾性分析。1978年至1999年间,28例患者接受了手术治疗;中位年龄36岁(范围19 - 68岁);19例为男性,9例为女性。所有患者均有疼痛和神经功能缺损症状。15例患者颈髓受累,5例颈胸段受累,6例胸髓受累,2例胸腰段受累。3例患者实现了全切,6例次全切,14例部分切除,仅5例进行了活检。19例患者术后接受了放疗。平均随访期为31.9个月(范围0.5 - 184个月)。18例为低级别星形细胞瘤,3例为间变性星形细胞瘤,7例为胶质母细胞瘤。低级别和高级别星形细胞瘤患者的中位生存期分别为184个月和8个月(p < 0.05)。低级别星形细胞瘤患者中,接受放疗和未接受放疗者的中位生存期分别为184个月和102个月。切除范围和放疗均未影响生存率。总之,组织学分级是脊髓星形细胞瘤患者生存的最显著预测因素。

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