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立体定向放射神经外科治疗颈静脉孔神经鞘瘤。

Stereotactic radio-neurosurgery for jugular foramen schwannomas.

机构信息

Neurosurgery Service and Gamma Knife Center, Lausanne University Hospital (CHUV), Rue du Bugnon 44-46, BH-08, CH-1011, Lausanne, Switzerland.

Faculty of Biology and Medicine (FBM), University of Lausanne (UNIL), Lausanne, Switzerland.

出版信息

Acta Neurochir (Wien). 2024 Aug 23;166(1):348. doi: 10.1007/s00701-024-06211-x.

Abstract

BACKGROUND

Stereotactic radiosurgery (SRS) represents a minimally invasive and valuable alternative for jugular foramen schwannomas (JFS), both as upfront and/or adjuvant treatment (in hybrid approaches).

METHODS

We conducted a retrospective review of our cases treated at the Lausanne University Hospital (CHUV) from June 2010 to October 2023. Eleven patients underwent SRS, among whom three had prior surgery, two in our center in the frame of a planned combined approach and one in another center. Two patients received "volume-staged" SRS. The mean age at SRS was 60 years (median 68; range 29-83). Cranial nerve (CN) symptoms were present in six patients, while five were asymptomatic. The mean tumor volume at SRS was 2.1 cc (median 1.2; range 0.068-7.3 cc), with a 12 Gy marginal dose prescribed in all cases.

RESULTS

The mean follow-up period was 3.9 years (median 2, range 1-7). Cranial nerve function improved after SRS in six patients, while five remained stable. At the last follow-up, all tumors showed a decrease in volume, except for one patient, who underwent surgery at 18 months after SRS, for volumetric increase at 6 and 12 months, with further XII CN palsy and medulla oblongata compression. Although tumor decreased at 18 months, such patient needed microsurgical resection for symptom persistence and was further controlled. The mean tumor volume at 1 year post-SRS was 1.6 cc (median 0.55; range 0.028-7.77 cc), at 2 years was 1.31 cc (median 0.76; range 0.19-5), and at 3 years was 1.32 cc (median 0.59; range 0.23-4.8). No adverse radiation events were observed.

CONCLUSIONS

Stereotactic radiosurgery is considered a safe and effective treatment for jugular foramen schwannomas, ensuring high rates of tumor control in all patients over the long term. The cranial nerve function improved after SRS in the 6 patients who had deficits and the other 5 patients who had no deficits remained asymptomatic. For larger tumors, combined/hybrid approaches can be a valuable alternative, to obtain tumor control and to preserve neurological function.

摘要

背景

立体定向放射外科(SRS)是治疗颈静脉孔神经鞘瘤(JFS)的一种微创且有价值的选择,无论是作为初始治疗还是辅助治疗(在混合治疗方法中)。

方法

我们对 2010 年 6 月至 2023 年 10 月在洛桑大学医院(CHUV)治疗的病例进行了回顾性研究。11 名患者接受了 SRS 治疗,其中 3 名患者之前接受过手术,2 名在我们中心计划的联合治疗框架内进行,1 名在另一家中心进行。2 名患者接受了“体积分期”SRS。SRS 时的平均年龄为 60 岁(中位数 68;范围 29-83)。6 名患者存在颅神经(CN)症状,而 5 名患者无症状。SRS 时的平均肿瘤体积为 2.1cc(中位数 1.2;范围 0.068-7.3cc),所有病例均给予 12Gy 边缘剂量。

结果

平均随访时间为 3.9 年(中位数 2,范围 1-7)。6 名患者在 SRS 后颅神经功能改善,5 名患者保持稳定。在最后一次随访时,除了 1 名患者在 SRS 后 18 个月因体积增加而进行手术外,所有肿瘤体积均缩小,在 SRS 后 6 个月和 12 个月时出现第 XII 颅神经麻痹和延髓受压。尽管肿瘤在 18 个月时缩小,但由于症状持续存在,该患者需要进行显微切除术,随后得到进一步控制。SRS 后 1 年肿瘤体积为 1.6cc(中位数 0.55;范围 0.028-7.77cc),2 年时为 1.31cc(中位数 0.76;范围 0.19-5),3 年时为 1.32cc(中位数 0.59;范围 0.23-4.8)。未观察到不良放射事件。

结论

立体定向放射外科被认为是治疗颈静脉孔神经鞘瘤的一种安全有效的方法,可确保所有患者在长期内获得高肿瘤控制率。在有缺陷的 6 名患者中,SRS 后颅神经功能改善,而在没有缺陷的 5 名患者中,其他 5 名患者保持无症状。对于较大的肿瘤,可以采用联合/混合方法作为一种有价值的替代方法,以获得肿瘤控制并保留神经功能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/33c4/11343977/42de41ed36fe/701_2024_6211_Fig1_HTML.jpg

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