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小型听神经瘤:手术结果与观察或放疗的对比

Small acoustic neuromas: surgical outcomes versus observation or radiation.

作者信息

Meyer Ted A, Canty Paul A, Wilkinson Eric P, Hansen Marlan R, Rubinstein Jay T, Gantz Bruce J

机构信息

Medical University of South Carolina, Department of Otolaryngology-HNS, Charleston, SC, USA, and Royal Children's Hospital, Department of Otolaryngology, Melbourne, Australia.

出版信息

Otol Neurotol. 2006 Apr;27(3):380-92. doi: 10.1097/00129492-200604000-00015.

Abstract

OBJECTIVE

Evaluate factors affecting outcomes of small acoustic neuroma (AN) removal via a middle cranial fossa (MCF) approach, and compare results to published data on observation and radiation therapy.

STUDY DESIGN

Retrospective chart review.

SETTING

Academic tertiary referral center.

METHODS

162 consecutive patients (ages 19-70) with unilateral AN (0.2-2.5 cm in largest dimension) removed through a MCF approach were reviewed focusing on preservation of hearing, facial nerve function and complications. One hundred thirteen patients had pre-operative word recognition scores (WRS)>70%.

RESULTS

Both tumor size and pre-operative WRS were related to post-operative WRS (p<0.01). Overall, at least some hearing was preserved in 94 (60%) of the 156 patients who had hearing before surgery. If the WRS was also >70% (N=113), 56 (50%) maintained WRS>70%. Importantly, WRS for 12 others improved to >70% after surgery. When the patients were stratified by tumor size, the patients with small tumors (2-10 mm) faired better than the overall group. At least some hearing was preserved in 65 (72%) of the 90 patients. If the WRS was also >70% (N=66), 39 (59%) maintained WRS>70%. WRS for eight others improved to >70% after surgery. When the tumor was 1.1-1.4 cm (N=34), the chance of preserving some hearing decreased to 42% (14/33). If the WRS was also >70% (N=23), 9 (39%) maintained WRS>70%. WRS for three others improved to >70% after surgery. When the tumor reached 1.5-2.5 cm (N=35), the hearing preservation rate was 43%. If the WRS was also >70% (N=24), only eight (33%) maintained WRS of 70%, and one other improved to >70%. The addition of intra-operative whole eighth nerve near field monitoring improved results during small tumor (<or=1.0 cm) removal preserving some hearing in 80% (32/40) and preserving >70% WRS in 76% (22/29) of those with >70% pre-operative WRS. Good facial nerve function (HB I-II) was achieved in 97% (86% HB I). When tumor size was <or=1.0 cm (N=93), however, good facial nerve function was obtained in 100% (94% HB I). Complications included CSF leak: 9 (5.5%); seizure: 2 (1.2%); and recurrence: 1 (0.6%).

CONCLUSION

Our results suggest that removal of unilateral AN through an MCF approach when the tumor is small and hearing is good provides the best opportunity for hearing preservation and normal facial nerve function. Observation historically results in tumor growth in young and middle-age patients with subsequent hearing loss. Radiation may prevent most tumors from growing, and more data are needed to determine long-term tumor control and hearing preservation rates.

摘要

目的

评估影响经中颅窝(MCF)入路切除小型听神经瘤(AN)疗效的因素,并将结果与已发表的关于观察和放射治疗的数据进行比较。

研究设计

回顾性病历审查。

研究地点

学术性三级转诊中心。

方法

回顾性分析162例连续接受MCF入路切除单侧AN(最大直径0.2 - 2.5 cm)的患者(年龄19 - 70岁),重点关注听力保留、面神经功能和并发症情况。113例患者术前言语识别得分(WRS)>70%。

结果

肿瘤大小和术前WRS均与术后WRS相关(p<0.01)。总体而言,术前有听力的156例患者中,94例(60%)至少保留了部分听力。若WRS也>70%(n = 113),则56例(50%)患者术后WRS仍>70%。重要的是,另有12例患者术后WRS提高至>70%。按肿瘤大小分层后,小型肿瘤(2 - 10 mm)患者的听力保留情况优于总体组。90例患者中有65例(72%)至少保留了部分听力。若WRS也>70%(n = 66),则39例(59%)患者术后WRS仍>70%。另有8例患者术后WRS提高至>70%。当肿瘤大小为1.1 - 1.4 cm(n = 34)时,保留部分听力的几率降至42%(14/33)。若WRS也>70%(n = 23),则9例(39%)患者术后WRS仍>70%。另有3例患者术后WRS提高至>70%。当肿瘤大小达到1.5 - 2.5 cm(n = 35)时,听力保留率为43%。若WRS也>70%(n = 24),仅8例(33%)患者术后WRS维持在70%,另有1例提高至>70%。术中增加第八对脑神经近场监测可改善小型肿瘤(≤1.0 cm)切除效果,术前WRS>70%的患者中,80%(32/40)保留了部分听力,76%(22/29)患者术后WRS>70%。面神经功能良好(House - Brackmann分级I - II级)的比例为97%(86%为I级)。然而,当肿瘤大小≤1.0 cm(n = 93)时,面神经功能良好的比例为100%(94%为I级)。并发症包括脑脊液漏:9例(5.5%);癫痫发作:2例(1.2%);复发:1例(0.6%)。

结论

我们的结果表明,对于小型且听力良好的单侧AN,经MCF入路切除可为听力保留和正常面神经功能提供最佳机会。历史上,观察会导致年轻和中年患者肿瘤生长并随后出现听力丧失。放射治疗可能会阻止大多数肿瘤生长,需要更多数据来确定长期肿瘤控制和听力保留率。

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