Westphal Manfred, Mohme Malte
Department of Neurosurgery, University Medical Center Hamburg Eppendorf, Hamburg, Germany.
Neurooncol Adv. 2024 Feb 13;6(Suppl 3):iii57-iii65. doi: 10.1093/noajnl/vdad138. eCollection 2024 Oct.
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.
脊髓室管膜瘤在组织学和遗传学上截然不同,严格分为髓内病变和髓外病变。髓内病变(SPE)属于世界卫生组织(WHO)2级,极少为3级,而髓外病变或黏液乳头型肿瘤(MPE)直到最近才被归为WHO 2级。主要区别在于,一般来说,2级髓内病变即使在完全切除后很少复发,也仍局限于原发局部部位。相比之下,MPE有在整个脑脊液腔隙扩散的能力,但也可通过谨慎的完全切除得到控制。我们在此回顾脊髓室管膜瘤的临床特征,对比不同类型,并描述从文献中发现的治疗这些病变的最佳方法,包括多学科方法。