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库斯I-II级前庭神经鞘瘤的显微手术:100例连续病例系列

Microsurgery of Koos I-II vestibular schwannomas: a case series of 100 consecutive patients.

作者信息

Mastronardi Luciano, Campione Alberto, Boccacci Fabio, Cacciotti Guglielmo, Carpineta Ettore, Giacobbo Scavo Carlo, Roperto Raffaelino, Stati Giovanni, Altamura Cristiana F, Alomari Amer A

机构信息

Department of Neurosurgery, San Filippo Neri Hospital, ASLRoma1, Rome, Italy.

Department of Neurosurgery, State Education Institution of Higher Professional Training, First Sechenov Moscow State Medical University under Ministry of Health, Moscow, Russia.

出版信息

J Neurosurg Sci. 2025 Apr;69(2):174-181. doi: 10.23736/S0390-5616.23.06014-9. Epub 2023 Jun 12.

Abstract

BACKGROUND

Treatment of small vestibular schwannomas (VS) depends on size, growth pattern, age, symptoms, co-morbidities. Watchful waiting, stereotactic radiosurgery and microsurgery are three valid options of treatment.

METHODS

We reviewed clinical sheets, surgical data and results of 100 consecutive patients with Koos Grade I-II VS, operated at our department via a retrosigmoid microsurgical approach between September 2010 and July 2021. Extent of resection was assessed as total, near-total or subtotal. The course of facial nerve (FN) around the tumor was classified as anterior (A), anterior-inferior (AI), anterior-superior (AS) and dorsal (D). FN function was assessed according to House-Brackmann (HB) Scale and hearing level according to AAO-HNS Classification.

RESULTS

Mean tumor size was 1.52 cm. FN course was mainly AS (46.0%) in the overall cohort; in Koos I VS, FN was AS in 83.3%. Postoperative FN function was HB I in 97% and HB II in 3% of cases. Hearing preservation (AAO-HNS class A-B) was possible in 63.2% of procedures. Total/near-total removal was achieved in 98%. Postoperative mortality was zero. Transient complications were observed in 8% of patients; permanent complications never occurred. Tumor remnant progression was observed in one case, 5 years after subtotal removal.

CONCLUSIONS

Microsurgery represents a valid option for management of VS, including Koos I-II grades, with an acceptable complication rate. In particular, in small VS long-term FN facial outcome, HP and total/near-total removal rate are favorable.

摘要

背景

小型前庭神经鞘瘤(VS)的治疗取决于肿瘤大小、生长模式、年龄、症状及合并症。密切观察、立体定向放射外科手术和显微外科手术是三种有效的治疗选择。

方法

我们回顾了2010年9月至2021年7月期间在我科通过乙状窦后显微手术入路治疗的100例连续的库斯I-II级VS患者的临床资料、手术数据及结果。切除范围评估为全切、近全切或次全切。肿瘤周围面神经(FN)走行分为前方(A)、前下方(AI)、前上方(AS)和后方(D)。根据House-Brackmann(HB)量表评估FN功能,根据美国耳鼻咽喉头颈外科学会(AAO-HNS)分类评估听力水平。

结果

平均肿瘤大小为1.52 cm。在整个队列中,FN走行主要为AS(46.0%);在库斯I级VS中,FN为AS的占83.3%。术后FN功能HB I级的病例占97%,HB II级的占3%。63.2%的手术实现了听力保留(AAO-HNS A-B级)。98%实现了全切/近全切。术后死亡率为零。8%的患者出现短暂并发症;未发生永久性并发症。1例患者在次全切术后5年观察到肿瘤残留进展。

结论

显微外科手术是治疗VS(包括库斯I-II级)的有效选择,并发症发生率可接受。特别是对于小型VS,长期FN面部预后、听力保留及全切/近全切率良好。

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