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马尾原发性硬脊膜内尤文肉瘤的磁共振成像表现:病例报告及文献复习

Magnetic resonance image findings of primary intradural Ewing sarcoma of the cauda equina: case report and review of the literature.

作者信息

Lozupone Emilio, Martucci Matia, Rigante Luigi, Gaudino Simona, Di Lella Giuseppe Maria, Colosimo Cesare

机构信息

Department of Bioimaging and Radiological Sciences, Catholic University School of Medicine, L.go A. Gemelli 8, 000168 Rome, Italy.

Department of Bioimaging and Radiological Sciences, Catholic University School of Medicine, L.go A. Gemelli 8, 000168 Rome, Italy.

出版信息

Spine J. 2014 Apr;14(4):e7-e11. doi: 10.1016/j.spinee.2013.09.024. Epub 2013 Oct 11.

Abstract

BACKGROUND CONTEXT

Involvement of the cauda equina in Ewing sarcoma (ES) is extremely rare, and only few cases are reported in literature. However, ES of cauda equina shares some neuroradiological features with other neoplasms that can involve the intradural space. Therefore, differential diagnosis with other tumors of cauda equina should be considered by neuroradiologists and neurosurgeons to provide appropriate treatment.

PURPOSE

To present a rare case of intradural extramedullary primary ES.

STUDY DESIGN

Case report.

METHODS

We report a case of a 44-year-old woman presenting with the rapid onset of cauda equina syndrome. Radiological analysis showed multiple intradural masses, extending from L1 to S3 level. After radical surgery, lesions were histologically defined as ES. We present a literature review, analyzing magnetic resonance image (MRI) features of primary intradural ES of the cauda equina.

RESULTS

Four cases of primitive ES arising from the cauda equina have been reported in the literature.

CONCLUSIONS

Because of the low number of reported cases, it is not possible to describe pathognomonic MRI findings for intradural ES of the cauda equina. However, few tumors show similar MRI features. Therefore, despite its rarity, intradural ES should be taken into account in the differential diagnosis of spinal tumors involving cauda equina.

摘要

背景

马尾神经受累于尤因肉瘤(ES)极为罕见,文献中仅有少数病例报道。然而,马尾神经的ES与其他可累及硬膜内间隙的肿瘤具有一些神经放射学特征。因此,神经放射科医生和神经外科医生应考虑与其他马尾神经肿瘤进行鉴别诊断,以提供恰当的治疗。

目的

报告一例罕见的硬膜内髓外原发性ES病例。

研究设计

病例报告。

方法

我们报告一例44岁女性,其马尾神经综合征起病迅速。影像学分析显示多个硬膜内肿块,从L1延伸至S3水平。根治性手术后,病变经组织学确诊为ES。我们进行了文献综述,分析了马尾神经原发性硬膜内ES的磁共振成像(MRI)特征。

结果

文献中已报道4例起源于马尾神经的原始ES病例。

结论

由于报道病例数量较少,无法描述马尾神经硬膜内ES的特征性MRI表现。然而,少数肿瘤具有相似的MRI特征。因此,尽管罕见,但在涉及马尾神经的脊柱肿瘤鉴别诊断中应考虑硬膜内ES。

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