Ryu Seong Jun, Kim Jong Yul, Kim Kyung Hyun, Park Jeong Yoon, Kuh Sung Uk, Chin Dong Kyu, Kim Keun Su, Cho Yong Eun, Kim Se Hoon
Department of Neurosurgery, Gangnam Severance Hospital, The Spine and Spinal Cord Institute, Yonsei University College of Medicine, 211, Eonju-ro Gangnam-gu, Seoul, 135-720, South Korea.
Department of Pathology, Severance Hospital, Yonsei University College of Medicine, Seoul, Korea.
Eur Spine J. 2016 Dec;25(12):4067-4079. doi: 10.1007/s00586-016-4475-7. Epub 2016 Mar 16.
To determine the biologic behavior and prognostic factors of spinal cord astrocytoma, we reviewed surgical and clinical outcomes. Due to the rarity of spinal cord astrocytoma, there is a lack of research regarding this type of tumor and malignant transformation.
We retrospectively reviewed the data from all patients on whom we performed spinal cord tumor removal between 1983 and 2014. Twenty-six patients were pathologically confirmed to have spinal cord astrocytoma or glioblastoma. Surgical extent and disease progression were confirmed by the surgeon based on operative findings, postoperative MRI, and outpatient department (OPD) follow-up.
Pain or neurological deficit was the chief complaint for all patients. With MRI studies, there is a tendency for high-grade astrocytomas to show as enhanced and heterogeneous images. Two of the low-grade astrocytomas showed malignant transformation over the course of 4 and 11 months, respectively. The overall survival (OS) for low-grade astrocytoma was 28-480 months (mean 156.38 months); the OS for high-grade astrocytoma was 1-36 months (mean 12.00 months).
Two of 12 low-grade cases showed malignant transformations at 4 and 11 months, respectively, based on pathological confirmation. With spinal cord astrocytomas, enhanced MRI results appeared similar to those of a malignant lesion. We suggest close observation and image correlation of low-grade astrocytomas, even when pathologically confirmed as low-grade. In this review, we found that histologic grade is the most important prognostic factor, although it is not always concordant with biologic behaviors.
为了确定脊髓星形细胞瘤的生物学行为和预后因素,我们回顾了手术及临床结果。由于脊髓星形细胞瘤罕见,针对此类肿瘤及恶性转化的研究较少。
我们回顾性分析了1983年至2014年间所有接受脊髓肿瘤切除术患者的数据。26例患者经病理证实患有脊髓星形细胞瘤或胶质母细胞瘤。手术范围和疾病进展由外科医生根据手术发现、术后MRI及门诊随访结果确定。
所有患者的主要症状为疼痛或神经功能缺损。MRI检查显示,高级别星形细胞瘤倾向于表现为强化且不均匀的图像。2例低级别星形细胞瘤分别在4个月和11个月的病程中发生了恶性转化。低级别星形细胞瘤的总生存期(OS)为28 - 480个月(平均156.38个月);高级别星形细胞瘤的OS为1 - 36个月(平均12.00个月)。
根据病理证实,12例低级别病例中有2例分别在4个月和11个月时发生了恶性转化。对于脊髓星形细胞瘤,MRI强化结果与恶性病变相似。我们建议即使低级别星形细胞瘤经病理证实为低级别,也应密切观察并进行图像对比。在本综述中,我们发现组织学分级是最重要的预后因素,尽管它并不总是与生物学行为一致。