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Intramedullary melanotic schwannoma of the cervical spine: A case report and literature review

机译:颈椎髓内黑色素瘤性神经鞘瘤1例并文献复习

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摘要

Intramedullary melanotic schwannomas (IMS) are rare lesions, with only 8 cases reported in the literature to date. We herein describe the case of a 40-year-old male patient with an IMS of the cervical cord, which, to the best of our knowledge, is the ninth reported case of IMS, and review the relevant literature. The patient presented with numbness of the left arm that gradually worsened over a period of 4 months. Magnetic resonance imaging (MRI) of the cervical spine with gadolinium enhancement revealed an intramedullary lesion at the level of C1-C2. The mass was T1 hyperintense, T2 hypointense and homogeneously enhanced. During surgery, an intramedullary dark gray lesion was identified and was partially removed. The left arm numbness partially subsided 2 weeks after surgery. Although rare, IMS is associated with characteristic MRI findings (T1 hyperintensity, T2 hypointensity and homogeneous enhancement) and MRI is the preferred method for evaluating lesions of the spinal cord. Correct diagnosis is crucial for management planning; therefore, immunohistochemical examination is required. In addition, IMS cases must be closely followed up, particularly when the mass cannot be completely resected.
机译:髓内黑变神经鞘瘤(IMS)是罕见的病变,迄今为止文献中仅报道了8例。在本文中,我们描述了一名40岁男性患者的颈髓IMS病例,据我们所知,这是第9例报告的IMS病例,并复习了相关文献。患者表现出左臂麻木,并在4个月内逐渐恶化。 g增强的颈椎磁共振成像(MRI)显示C1-C2水平的髓内病变。肿块为T1高强度,T2低水平且均一增强。在手术过程中,发现了髓内暗灰色病变并被部分切除。术后2周左臂麻木部分消退。尽管很少见,但IMS与特征性MRI表现(T1高信号,T2低信号和均质增强)相关,并且MRI是评估脊髓损伤的首选方法。正确的诊断对于管理计划至关重要;因此,需要进行免疫组织化学检查。此外,必须密切跟踪IMS病例,尤其是当肿块无法完全切除时。

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