Gui Chloe, Canthiya Luxshikka, Zadeh Gelareh, Suppiah Suganth
MacFeeters-Hamilton Centre for Neuro Oncology, Princess Margaret Cancer Research Center, Toronto, Ontario, Canada.
Division of Neurosurgery, University of Toronto, Toronto, Ontario, Canada.
Neurooncol Adv. 2024 Jul 17;6(Suppl 3):iii83-iii93. doi: 10.1093/noajnl/vdae067. eCollection 2024 Oct.
Nerve sheath tumors are the most common tumors of the spine after meningiomas. They include schwannomas, neurofibroma, and malignant peripheral nerve sheath tumors. These can arise sporadically or in association with tumor predisposition syndromes, including neurofibromatosis type 1, neurofibromatosis type 2, and schwannomatosis. Though surgery is the traditional mainstay of treatment for these tumors, the discovery of the genetic and molecular basis of these diseases in recent decades has prompted investigation into targeted therapies. Here, we give a clinical overview of spinal nerve sheath tumors, their imaging features, current management practices, and explore ongoing advances in systemic therapies.
神经鞘瘤是继脑膜瘤之后脊柱最常见的肿瘤。它们包括施万细胞瘤、神经纤维瘤和恶性外周神经鞘瘤。这些肿瘤可散发性出现,或与肿瘤易感综合征相关,包括1型神经纤维瘤病、2型神经纤维瘤病和施万细胞瘤病。尽管手术是这些肿瘤传统的主要治疗方法,但近几十年来这些疾病遗传和分子基础的发现促使人们对靶向治疗进行研究。在此,我们对脊柱神经鞘瘤进行临床概述,介绍其影像学特征、当前的治疗方法,并探讨全身治疗方面的最新进展。