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髓外起源的原发性脊柱黑色素瘤:三例报告及文献系统综述

Primary spinal melanoma of extramedullary origin: a report of three cases and systematic review of the literature.

作者信息

Liu Q-Y, Liu A-M, Li H-G, Guan Y-B

机构信息

Department of Radiology, Zengcheng People's Hospital, Zengcheng, Guangdong Province, China; Department of Radiology, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou, Guangdong Province, China.

Division of Neurosurgery, Department of Surgery, Sun Yat-sen Memorial Hospital, Sun Yat-sen University , Guangzhou, Guangdong Province, China.

出版信息

Spinal Cord Ser Cases. 2015 Jul 9;1:15003. doi: 10.1038/scsandc.2015.3. eCollection 2015.

Abstract

STUDY DESIGN

A review of the literature and three case reports.

OBJECTIVES

Primary spinal melanoma (PSM) of extramedullary origin is a rare malignant condition with limited current literature in regards to its clinical course, magnetic resonance imaging (MRI) findings, treatment strategies and prognosis. We reported here three cases of PSM of extramedullary origin.

SETTING

China, Guangzhou.

METHODS

We report three cases of PSM of extramedullary origin. The clinical and radiological findings of these cases were retrospectively analyzed.

RESULTS

The three cases were all of males aged 39, 47 and 76 years, respectively. The duration of their symptoms was 3 weeks, 2 months and 11 months respectively. The extramedullary tumors were all well-defined solitary tumors and were located at C4-5, L2-3 and T9-10, respectively. In one case, involvement of the intervertebral foramen was found. Preoperative MRI showed hyperintense T1W signals and hypointense T2W signals in all three cases and all tumors were clinically misdiagnosed as schwannomas. The patients received total or subtotal resection surgery without radiotherapy or chemotherapy. Patients were alive at 18 months, 27 months and 36 months postoperative follow-up, respectively.

CONCLUSION

PSM of extramedullary origin is a rare malignant tumor that shows characteristic findings on MRI. Surgical resection is the preferred treatment strategy.

摘要

研究设计

文献综述及三例病例报告。

目的

髓外原发性脊髓黑色素瘤(PSM)是一种罕见的恶性疾病,目前关于其临床病程、磁共振成像(MRI)表现、治疗策略及预后的文献有限。我们在此报告三例髓外原发性脊髓黑色素瘤病例。

地点

中国广州。

方法

我们报告三例髓外原发性脊髓黑色素瘤病例。对这些病例的临床和影像学表现进行回顾性分析。

结果

三例患者均为男性,年龄分别为39岁、47岁和76岁。其症状持续时间分别为3周、2个月和11个月。髓外肿瘤均为边界清晰的孤立性肿瘤,分别位于C4 - 5、L2 - 3和T9 - 10。其中一例发现椎间孔受累。术前MRI显示三例患者的肿瘤在T1加权像上均为高信号,在T2加权像上均为低信号,所有肿瘤在临床上均被误诊为神经鞘瘤。患者接受了全切除或次全切除手术,未进行放疗或化疗。术后随访18个月、27个月和36个月时患者均存活。

结论

髓外原发性脊髓黑色素瘤是一种罕见的恶性肿瘤,在MRI上有特征性表现。手术切除是首选的治疗策略。

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