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Primary Intramedullary Spinal Sarcoma : A Case Report and Review of the Current Literatures

机译:原发性髓内脊髓肉瘤:一例报道及最新文献复习

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摘要

Primary central nervous system (CNS) sarcomas are exceedingly rare, and, to the best of our knowledge, there has not yet been a report of intramedullary sarcoma. Here, we report a primary intradural intramedullary sarcoma of the spinal cord in a four-year-old boy who presented with low back pain and a radiculopathy involving both lower extremities. The tumor showed significant enhancement on magnetic resonance (MR) images due to its extreme vascularity. Gross total tumor removal was performed with microelectrical pulse recording, and the patient also received adjuvant radiotherapy and chemotherapy. After the operation, the patient's sensory deficits were improved. Because CNS dissemination is common, entire neuraxis evaluation is essential, although there was no evidence of dissemination in this case. The prognosis of primary CNS sarcoma is poor due to infiltrative nature and early CNS dissemination is common, and the treatment of choice is radical surgical resection. Adjuvant therapy is also beneficial with radiotherapy and chemotherapy.
机译:原发性中枢神经系统(CNS)肉瘤极为罕见,据我们所知,尚未有髓内肉瘤的报道。在这里,我们报道了一个四岁男孩的原发性硬脑膜内髓内肉瘤,该男孩表现出腰背痛和涉及下肢的神经根病。由于其极强的血管性,该肿瘤在磁共振(MR)图像上显示出明显的增强。用微电脉冲记录进行总的肿瘤切除,患者还接受了辅助放疗和化疗。手术后,患者的感觉缺陷得到改善。由于中枢神经系统的传播很普遍,因此,尽管没有证据表明有传播的迹象,但整个神经功能评估都是必不可少的。由于具有浸润性,原发性中枢神经系统肉瘤的预后较差,中枢神经系统早期扩散是常见的,选择的治疗方法是根治性手术切除。辅助疗法对放射疗法和化学疗法也有益。

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