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原发性孤立性迷路内神经鞘瘤:7例报告及文献复习

Primary solitary intralabyrinthine schwannoma: A report of 7 cases and a review of the literature.

作者信息

Shupak Avi, Holdstein Yehuda, Kaminer Margalit, Braverman Itzhak

机构信息

Unit of Otoneurology, Lin Medical Center, Rothschild Ave. 35, Haifa 3515209, Israel.

出版信息

Ear Nose Throat J. 2016 Dec;95(12):481-491.

Abstract

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 T1-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.

摘要

迷路内神经鞘瘤(ILSs)是一种罕见的良性肿瘤,起源于前庭蜗神经迷路内远端分支的施万细胞鞘。它们最初不累及内耳道,尽管后期可能会发展至此。这些病变可发生于耳蜗内、起源于前庭,或在极少数情况下发生于半规管。从这些部位,肿瘤可能通过前庭阶外淋巴间隙与前庭前部之间的解剖连接扩散。因此,以耳蜗为中心的ILSs可能累及前庭,而起源于前庭终器的肿瘤则会累及耳蜗。主要症状和体征包括进行性或突发性感音神经性听力损失(超过95%的患者会出现),以及耳鸣和眩晕。磁共振成像特征包括边界清晰,在薄层、重度T2加权三维图像上呈低信号,在T1加权图像上给予钆剂后有明显强化。我们描述了在我们两所机构治疗的7例原发性ILSs病例。我们还讨论了进行全面耳神经学评估的必要性,该评估应包括功能紊乱以及MRI所显示的肿瘤位置,并描述了治疗方案。

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