首页> 外文期刊>Acta Neurochirurgica >Spinal intradural primary germ cell tumour--review of literature and case report.
【24h】

Spinal intradural primary germ cell tumour--review of literature and case report.

机译:脊髓硬膜内原发性生殖细胞肿瘤-文献复习和病例报告

获取原文
获取原文并翻译 | 示例
           

摘要

BACKGROUND: Primary spinal cord germ cell tumour is a rare tumour. We herein review the tumour characteristics, associated risk factors, treatment policy, and patterns of failure of primary intradural germ cell tumour. METHOD: We conducted a PUBMED search using a combination of keywords such as "spinal germ cell tumor," germinoma, identified 19 cases of primary spinal germ cell tumour. Clinical features, pathologic characteristics, and treatment details of these patients including status at follow-up were noted from respective case reports. We also describe a case of a young Indian patient of intradural extramedullary germ cell tumour treated with a combination of surgery, chemotherapy, and radiotherapy. FINDINGS: The median age at presentation was 24 years. The most common location of the tumour was thoracic (40%). Beta-HCG overproduction was noted in 40% of the patients. Most patients were treated with a combination of surgery, radiation therapy, and systemic chemotherapy. Median follow-up was 16.5 months. Recurrence was observed in 10% of the patients, all in beta-HCG over-producing tumours. The illustrative case was a 28-year male, presenting with pain in lower back and both lower limbs for 2 months. Magnetic resonance imaging spine showed an inhomogeneous hyperintense soft tissue mass at L(2)-L(4) spinal level. He was treated with complete surgical excision and four cycles of chemotherapy with BEP regimen following a histological diagnosis of non-seminomatous germ cell tumour. Palliative irradiation to the lumbar spine was given on progression at 3 months. The patient eventually succumbed to his condition, due to compressive transverse myelitis possibly due to cervical cord metastasis. CONCLUSION: Limited surgery followed by upfront radiation therapy and adjuvant chemotherapy is the optimal management of this rare group of tumour. Omission of radiation therapy from the treatment armamentarium might engender local recurrence and spinal dissemination at first failure.
机译:背景:原发性脊髓生殖细胞肿瘤是一种罕见的肿瘤。我们在这里回顾了原发性硬脑膜内生殖细胞肿瘤的肿瘤特征,相关的危险因素,治疗策略和失败模式。方法:我们结合关键词“脊髓生殖细胞肿瘤”,生殖细胞瘤进行了PUBMED搜索,确定了19例原发性脊柱生殖细胞肿瘤。从各自的病例报告中记录了这些患者的临床特征,病理特征和治疗细节,包括随访情况。我们还描述了一起手术,化学疗法和放射疗法相结合治疗的年轻印度硬膜内髓外生殖细胞肿瘤患者的病例。结果:演讲时的中位年龄为24岁。肿瘤最常见的部位是胸部(40%)。在40%的患者中发现了β-HCG的过量生产。大多数患者接受了外科手术,放射疗法和全身化疗的联合治疗。中位随访时间为16.5个月。 β-HCG过度产生的肿瘤中有10%的患者出现了复发。该例病例为28岁男性,下背部和双下肢疼痛持续2个月。磁共振成像脊柱在L(2)-L(4)脊柱水平显示不均匀的高强度软组织肿块。在组织学诊断为非精原细胞性生殖细胞肿瘤后,他接受了完全外科切除和BEP方案化疗四个周期的治疗。在3个月的进展过程中对腰椎进行姑息照射。由于受压性脊髓炎可能归因于颈索转移,患者最终屈服于病情。结论:有限的手术后再进行前期放疗和辅助化疗是这种罕见肿瘤的最佳治疗方法。治疗武器库遗漏放射治疗可能会导致局部复发和初次失败时脊柱扩散。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号