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成人颈椎髓内未成熟畸胎瘤伴转移复发

Cervical intramedullary immature teratoma with metastatic recurrence in an adult.

作者信息

Han Z, Du Y, Qi H, Zheng S, Yin W

机构信息

Department of Neurosurgery, Peking University Shenzhen Hospital , Shenzhen, P.R. China.

Department of Nursing, School of Medical Technology and Nursing, Shenzhen Polytechnic , Shenzhen, P.R. China.

出版信息

Spinal Cord Ser Cases. 2015 Jul 9;1:15006. doi: 10.1038/scsandc.2015.6. eCollection 2015.

Abstract

STUDY DESIGN

Case report.

OBJECTIVES

We present for the first time an adult patient with cervical intramedullary immature teratoma with metastatic recurrence.

SETTING

Peking university Shenzhen Hospital, Shenzhen, China.

METHODS

A 30-year-old woman presented with rapidly progressive quadriplegia. Magnetic resonance imaging (MRI) revealed an intramedullary tumor occupying C1-C2 of the upper spinal cord. An urgent operation, consisting of decompression by laminectomy and tumor gross resection, was performed under a preoperative diagnosis of spinal glioma. The histological diagnosis was immature teratoma. The patient received local radiotherapy after gross total resection. The serum alpha fetoprotein (AFP) and human chorionic gonadotropin (HCG) levels were normal postoperatively, until these were evaluated on the 10th month with neurological deterioration. Metastatic recurrences were demonstrated on MRI with lesions located at the levels of C5-C6 and T11-12. Removal of the second tumors was performed and the pathological examination identified a malignant germ cell tumor (yolk sac tumor). The patient was then referred to chemotherapy and radiotherapy.

RESULTS

No tumor regrowth was encountered and the patient remained stable for 6 months after adjuvant therapy.

CONCLUSION

Immature teratoma should be included in the differential diagnosis of holocord tumors in the adult with rapidly progressing symptoms and if found should be radically excised if possible. Adjuvant therapy should be the salvage therapy for this recurrent tumor.

摘要

研究设计

病例报告。

目的

我们首次报告一例成年颈髓内未成熟畸胎瘤伴转移复发患者。

地点

中国深圳北京大学深圳医院。

方法

一名30岁女性出现快速进展性四肢瘫痪。磁共振成像(MRI)显示脊髓髓内肿瘤占据上颈髓C1 - C2节段。在术前诊断为脊髓胶质瘤的情况下,进行了紧急手术,包括椎板切除减压和肿瘤全切术。组织学诊断为未成熟畸胎瘤。患者在肿瘤全切术后接受了局部放疗。术后血清甲胎蛋白(AFP)和人绒毛膜促性腺激素(HCG)水平正常,直到第10个月评估时出现神经功能恶化。MRI显示转移复发,病变位于C5 - C6和T11 - 12节段。进行了第二次肿瘤切除,病理检查确诊为恶性生殖细胞瘤(卵黄囊瘤)。随后患者接受化疗和放疗。

结果

辅助治疗后未出现肿瘤复发,患者在6个月内病情稳定。

结论

对于有快速进展症状的成年全脊髓肿瘤患者,未成熟畸胎瘤应列入鉴别诊断范围,若发现应尽可能根治性切除。辅助治疗应为该复发性肿瘤的挽救性治疗。

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