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听神经瘤及其他桥小脑角肿瘤切除患者听力的保留

Preservation of hearing in patients undergoing excision of acoustic neuromas and other cerebellopontine angle tumors.

作者信息

Tator C H, Nedzelski J M

出版信息

J Neurosurg. 1985 Aug;63(2):168-74. doi: 10.3171/jns.1985.63.2.0168.

DOI:10.3171/jns.1985.63.2.0168
PMID:3874935
Abstract

Microsurgical techniques have made it possible to identify and preserve the cochlear nerve from its origin at the brain stem and along its course through the internal auditory canal in patients undergoing removal of small or medium-sized acoustic neuromas or other cerebellopontine angle (CPA) tumors. In a consecutive series of 100 patients with such tumors operated on between 1975 and 1981, an attempt was made to preserve the cochlear nerve in 23. The decision to attempt to preserve hearing was based on tumor size and the degree of associated hearing loss. In cases of unilateral acoustic neuroma, the criteria for attempted preservation of hearing were tumor size (2.5 cm or less), speech reception threshold (50 dB or less), and speech discrimination score (60% or greater). In patients with bilateral acoustic neuromas or tumors of other types, the size and hearing criteria were significantly broadened. All patients were operated on through a suboccipital approach. Hearing was preserved postoperatively in six (31.6%) of the 19 patients with unilateral acoustic neuromas, although the cochlear nerve was preserved in 16. Of the six patients with postoperative hearing, three retained excellent hearing, and the other three had only sound awareness and poor discrimination. Hearing was preserved in three cases with other CPA tumors, including an epidermoid cyst and small petrous meningiomas in the internal auditory canal. Of the two cases with bilateral tumors, hearing was preserved in one. Of the 23 patients in whom hearing preservation was attempted, nine (39.1%) had some postoperative hearing, which in six was equal to or better than the preoperative level. Thus, it is worthwhile to attempt hearing preservation in selected patients with CPA tumors.

摘要

对于接受中小型听神经瘤或其他桥小脑角(CPA)肿瘤切除手术的患者,显微外科技术已能够在脑干处识别并保留从其起源处开始并沿其在内耳道走行的蜗神经。在1975年至1981年间连续接受此类肿瘤手术的100例患者中,有23例尝试保留蜗神经。尝试保留听力的决定基于肿瘤大小和相关听力损失程度。对于单侧听神经瘤病例,尝试保留听力的标准为肿瘤大小(2.5厘米或更小)、言语接受阈值(50分贝或更低)以及言语辨别得分(60%或更高)。对于双侧听神经瘤或其他类型肿瘤的患者,大小和听力标准显著放宽。所有患者均通过枕下入路进行手术。19例单侧听神经瘤患者中有6例(31.6%)术后听力得以保留,尽管有16例蜗神经得以保留。在6例术后有听力的患者中,3例保留了极佳的听力,另外3例仅有声音感知且辨别能力差。在3例其他CPA肿瘤患者中听力得以保留,包括1例表皮样囊肿和2例内耳道小岩骨脑膜瘤。在2例双侧肿瘤患者中,有1例听力得以保留。在尝试保留听力的23例患者中,9例(39.1%)术后有一定听力,其中6例等于或优于术前水平。因此,对于部分CPA肿瘤患者尝试保留听力是值得的。

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