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Thoracolumbar intramedullary subependymoma with multiple cystic formation: a case report and review

机译:胸腰椎髓内膜下室囊肿伴多囊性形成:一例报告并复习

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BackgroundAn intramedullary subependymoma is rare, particularly in the thoracolumbar region. Moreover, a radiographical obvious cystic formation of subependymoma of spinal cord rarely occurs in comparison to ependymoma.Case reportA 57-year-old woman presented with paraparesis. MRI revealed a multinodular and multicystic lesion in the spinal cord that was difficult to diagnose correctly. Intraoperative observation via midline myelotomy revealed a grayish, gelatinous solid mass with an eccentric localization. In addition, DREZtomy on the caudal side of the tumor revealed cystic formation. The cyst was punctured and xanthochromic fluid was collected. Attenuation of motor evoked potential (MEP) resulted in the partial removal of tumor. A pathological examination revealed the mass to be a subependymoma. The patient experienced transient worsening of symptoms, but improved gradually. No adjuvant radiosurgery was administered. Follow-up estimation 30?months after surgery revealed no evidences of regrowth.ConclusionsThis report presents this rare case, a review of the literature associated with thoracolumbar subependymomas, and a discussion of the clinical and radiographical characteristics...
机译:背景髓内膜下室膜瘤很少见,特别是在胸腰椎区域。而且,与室管膜瘤相比,很少有影像学上明显的脊髓性室管膜下囊性囊肿形成。病例报告一名57岁女性出现轻瘫。 MRI显示脊髓内有多结节和多囊性病变,难以正确诊断。通过中线肌切开术进行的术中观察显示偏心定位的灰色,凝胶状固体团块。另外,在肿瘤尾侧的DREZtomy显示出囊性形成。穿刺囊肿并收集黄变液。运动诱发电位(MEP)的减弱导致肿瘤的部分切除。病理检查发现该肿块为室管膜下瘤。患者经历了短暂的症状恶化,但逐渐好转。没有进行辅助放射外科手术。手术后30个月的随访估计没有发现再生长的迹象。结论本报告介绍了这种罕见病例,回顾了与胸腰膜室间隔膜瘤相关的文献,并讨论了临床和放射学特征...

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