Stereotactic radio-neurosurgery for jugular foramen schwannomas.

IF 1.9 3区 医学 Q3 CLINICAL NEUROLOGY
Camil Bourhila, Cristian Cotrutz, Roy Thomas Daniel, Mercy George, Luis Schiappacasse, David Patin, Marc Levivier, Constantin Tuleasca
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引用次数: 0

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-th 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.

Abstract Image

立体定向放射神经外科手术治疗颈静脉裂孔瘤。
背景:立体定向放射外科(SRS)是治疗颈静脉裂孔瘤(JFS)的一种微创且有价值的替代方法,既可作为前期治疗,也可作为辅助治疗(混合方法):我们对2010年6月至2023年10月在洛桑大学医院(CHUV)接受治疗的病例进行了回顾性分析。11名患者接受了SRS治疗,其中3人曾接受过手术,2人在本中心接受了计划中的联合治疗,1人在其他中心接受了手术。两名患者接受了 "体积分期 "SRS。接受 SRS 时的平均年龄为 60 岁(中位数为 68 岁;范围为 29-83 岁)。六名患者出现颅神经(CN)症状,五名无症状。SRS 时的平均肿瘤体积为 2.1 cc(中位数为 1.2;范围为 0.068-7.3 cc),所有病例的边缘剂量均为 12 Gy:平均随访时间为3.9年(中位数为2年,范围为1-7年)。6例患者的颅神经功能在SRS后得到改善,5例保持稳定。在最后一次随访中,除一名患者在SRS术后18个月接受手术外,其他患者的肿瘤体积均有所缩小,但在6个月和12个月时肿瘤体积增大,并进一步出现第十二CN麻痹和延髓受压。虽然肿瘤在18个月时有所缩小,但该患者因症状持续存在而需要进行显微手术切除,并进一步得到控制。SRS术后1年的平均肿瘤体积为1.6cc(中位数0.55;范围0.028-7.77cc),2年为1.31cc(中位数0.76;范围0.19-5),3年为1.32cc(中位数0.59;范围0.23-4.8)。未观察到不良放射事件:立体定向放射手术被认为是治疗颈静脉裂孔瘤的一种安全有效的方法,能确保所有患者的肿瘤长期得到较高的控制率。6 名出现功能障碍的患者在接受 SRS 治疗后颅神经功能有所改善,而另外 5 名没有功能障碍的患者仍无症状。对于较大的肿瘤,联合/混合方法是一种有价值的选择,既能控制肿瘤,又能保护神经功能。
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来源期刊
Acta Neurochirurgica
Acta Neurochirurgica 医学-临床神经学
CiteScore
4.40
自引率
4.20%
发文量
342
审稿时长
1 months
期刊介绍: The journal "Acta Neurochirurgica" publishes only original papers useful both to research and clinical work. Papers should deal with clinical neurosurgery - diagnosis and diagnostic techniques, operative surgery and results, postoperative treatment - or with research work in neuroscience if the underlying questions or the results are of neurosurgical interest. Reports on congresses are given in brief accounts. As official organ of the European Association of Neurosurgical Societies the journal publishes all announcements of the E.A.N.S. and reports on the activities of its member societies. Only contributions written in English will be accepted.
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