原发性孤立性脑内神经鞘瘤7例报告并文献复习

A. Shupak, Y. Holdstein, M. Kaminer, I. Braverman
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引用次数: 5

摘要

雪花蛋白内神经鞘瘤(ILSs)是一种罕见的良性肿瘤,起源于前庭耳蜗神经雪花蛋白内远端分支的雪旺细胞鞘。他们最初没有内耳道受累,尽管这可能会在以后发展。这些病变可发生在耳蜗内部,起源于前庭,或在极少数情况下,在半规管中发展。从这些部位开始,扩散可能通过前庭阶梯淋巴周围间隙和前庭之间的解剖连接发生。因此,以耳蜗为中心的il - ss可能累及前庭,而起源于前庭末端器官的il - ss会到达耳蜗。体征和症状包括进行性或突发性感音神经性听力丧失(95%以上的患者发生),以及耳鸣和眩晕。磁共振成像特征为薄层明显边界和低密度,重t2加权3D图像,ti加权图像加钆后增强强。我们描述了在我们的两个机构管理的7例原发性ILS。我们还讨论了需要进行全面的耳神经系统评估,包括功能紊乱和肿瘤位置的MRI描述,我们描述了治疗方案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Primary Solitary Intralabyrinthine Schwannoma: A Report of 7 Cases and a Review of the Literature
Intralabyrinthine schwannomas (ILSs) are uncommon benign tumors that originate in the Schwann cell sheath of the intralabyrinthine distal branches of the vestibulocochlear nerve. They have no initial involvement in the internal auditory canal although that might develop later. These lesions can arise inside the cochlea, originate in the vestibule or, in rare cases, develop in the semicircular canals. From these sites, spread might take place via the anatomic connections between the perilymphatic spaces in the scala vestibuli and the anterior vestibule. Thus, ILSs centered in the cochlea might involve the vestibule, and those originating in the vestibular end organs would reach the cochlea. Presenting signs and symptoms include a progressive or sudden sensorineural hearing loss (which occurs in more than 95% of patients), as well as tinnitus and vertigo. Magnetic resonance imaging characteristics include sharp circumscription and hypointensity on thin, heavily T2-weighted 3D images and strong enhancement after gadolinium administration on TI-weighted images. We describe a series of 7 cases of primary ILS that were managed at two of our institutions. We also discuss the need for a comprehensive otoneurologic evaluation that encompasses the functional derangement and the tumor location as delineated by MRI, and we describe the treatment options.
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