Cervical Intradural Extramedullary Melanocytoma , Associated with Nevus of Ito. Recurrence and Long-Term Outcome

Q4 Medicine
A. Tamimi, F. Obeidat, Nosaiba T. Al Ryalat, M. Juweid, S. Jabaiti, Yazen Olimat, Rahma M. Doudeen, Almustafa Sahar, Zaid Abuajamieh, Majed Ftaiha, I. Tamimi
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引用次数: 0

Abstract

Background: Melanocytoma is a rare pigmented central nervous tumor. In the spine, it may develop in meninges, extramedullary or intramedullary. It usually has good outcome after total excision. Case report: A 40-year-old male patient was admitted to our hospital 12 years ago with a 3-month history of progressive neck pain and difficulty walking. On clinical examination, he showed upper dorsal bilateral gray blue hyperpigmentation, quadriparesis and bilateral hypoesthesia below C4. Cervical magnetic resonance imaging (MRI) T1-weighted images without contrast showed a C3-C4 intradural, extramedullary lesion. The patient underwent total microsurgical resection of the lesion. Histological and immunohistochemical analyses confirmed the diagnosis of melanocytoma. Another skin biopsy of the abnormal area showed histological findings of a blue skin nevus. Eight years after resection the patient presented with recurrent symptoms, which were similar to his initial presentation. Cervical MRI showed an intradural extramedullary tumor anterior to the spinal cord at the same C3-C4 level. The patient underwent a second complete tumor excision and melanocytoma was confirmed histologically. The patient significantly improved and remained well at last follow-up. Conclusions: Intradural extra- or intramedullary melanocytoma is a rare benign tumor that frequently recurs but usually has good outcome following total excision. Keywords: Spinal cord, Meningeal, Melanocytoma, Extramedullary, Skin Nevus of Ito, Outcome
宫颈硬膜内髓外黑色素细胞瘤,伴伊藤痣。复发和长期结果
背景:黑色素细胞瘤是一种罕见的中枢神经色素性肿瘤。在脊柱,它可以在脑膜,髓外或髓内发展。全切除后通常有良好的预后。病例报告:一名40岁男性患者12年前因进行性颈部疼痛和行走困难3个月入院。临床检查显示双侧上背灰蓝色色素沉着,四肢麻痹和双侧C4以下感觉减退。宫颈磁共振成像(MRI)未经对比的t1加权图像显示C3-C4硬膜内、髓外病变。患者接受了全显微外科手术切除病变。组织学和免疫组织化学分析证实了黑素细胞瘤的诊断。另一个异常区域的皮肤活检显示了一个蓝色皮肤痣的组织学发现。术后8年,患者出现复发性症状,与最初的表现相似。颈椎MRI显示硬膜内髓外肿瘤位于脊髓前同一C3-C4水平。患者接受了第二次肿瘤完全切除,组织学证实为黑色素细胞瘤。病人在最后的随访中有明显的改善和保持良好。结论:硬膜内、髓外或髓内黑色素细胞瘤是一种罕见的良性肿瘤,常复发,但全切除后预后良好。关键词:脊髓,脑膜,黑素细胞瘤,髓外,伊藤皮肤痣,结果
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来源期刊
Jordan Medical Journal
Jordan Medical Journal Medicine-Medicine (all)
CiteScore
0.20
自引率
0.00%
发文量
33
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