脊髓上皮瘤

IF 3.7 Q1 CLINICAL NEUROLOGY
Neuro-oncology advances Pub Date : 2024-02-13 eCollection Date: 2024-10-01 DOI:10.1093/noajnl/vdad138
Manfred Westphal, Malte Mohme
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引用次数: 0

摘要

脊髓外胚层瘤在组织学和遗传学上截然不同,因此可严格细分为髓内病变和髓外病变。髓内病变(SPE)被定为世卫组织 2 级,极少数为 3 级,而髓外病变或髓外肌瘤(MPE)最近才被定为世卫组织 2 级。主要区别在于,一般来说,2 级的髓内病变仍局限于局部原发部位,即使在完全切除后很少复发。相比之下,MPE 有能力扩散到整个脑脊液区,但也可以通过谨慎的完全切除术加以控制。我们在此回顾脊髓外胚瘤的临床特征,对比不同实体,并介绍文献中发现的治疗这些病变的最佳方法,包括跨学科方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Spinal ependymal tumors.

Spinal ependymomas are strictly to be subdivided into intramedullary lesions and extramedullary lesions as they are histologically and genetically distinct. Whereas the intramedullary lesions (SPE) are assigned to the WHO grade 2 and very rarely grade 3, the extramedullary lesions or myxopapilary tumors (MPE) are only as recently also assigned to WHO grade 2. The major difference is that in general, an intramedullary lesion of grade 2 remains confined to the local site of origin, even when rarely recurring after complete resection. In contrast, the MPEs have the capacity to spread throughout the cerebrospinal fluid compartment but can also be controlled by cautious complete resection. We here review the clinical features of spinal ependymomas, contrasting the entities, and describe the treatment found best from the literature to manage these lesions including interdisciplinary approaches.

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来源期刊
CiteScore
6.20
自引率
0.00%
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审稿时长
12 weeks
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