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立体定向放射外科治疗前庭神经鞘瘤后辐射诱导的小脑前下动脉假性动脉瘤:直接手术观察到的特征。

Radiation-induced anterior inferior cerebellar artery pseudoaneurysm after stereotactic radiosurgery for vestibular schwannoma: features observed by direct surgery.

机构信息

Department of Neurosurgery, Fujita Health University Okazaki Medical Center, Okazaki, Japan.

Department of Neurosurgery, Fujita Health University, Toyoake, Japan.

出版信息

Br J Neurosurg. 2023 Dec;37(6):1675-1679. doi: 10.1080/02688697.2021.1940856. Epub 2021 Jun 21.

DOI:10.1080/02688697.2021.1940856
PMID:34148476
Abstract

BACKGROUND

In vestibular schwannoma (VS) patients treated with stereotactic radiosurgery (SRS), radiation-induced pseudoaneurysm is a rare long-term complication. To the best of our knowledge, there has been only one report of direct surgery in ruptured cases, and the optimal strategy for direct surgery is yet to be clarified. This case report describes a case of ruptured VS-related SRS-induced pseudoaneurysm that was successfully treated by direct surgery.

CASE PRESENTATION

A 57-year -old man underwent SRS for VS, and the tumour was well controlled after the SRS. Nine years after the SRS, however, he developed subarachnoid haemorrhage, and a SRS-induced distal anterior inferior cerebellar artery aneurysm was detected on the surface of the tumour. During the trapping surgery, the aneurysm was embedded in the tumour, and it was difficult to separate the aneurysm and tumour. Besides, the facial nerve and tumour restricted exposure of the parent artery. The parent artery proximal to the aneurysm could only be exposed by resecting caudal part of the tumour. The aneurysm was trapped with permanent clips and it was pathologically diagnosed as pseudoaneurysm.

CONCLUSION

It was suggested that the VS-related SRS-induced pseudoaneurysm is tightly adhered with surrounding structures and exposure of the parent artery could be limited due to the tumour and facial nerve. In this case report, we describe detailed intraoperative findings that will be useful for developing strategies for trapping surgery in future.

摘要

背景

在接受立体定向放射外科(SRS)治疗的前庭神经鞘瘤(VS)患者中,辐射诱导的假性动脉瘤是一种罕见的长期并发症。据我们所知,仅有一例破裂病例的直接手术报告,直接手术的最佳策略仍需阐明。本病例报告描述了一例成功通过直接手术治疗的破裂性 SRS 诱导假性动脉瘤。

病例介绍

一名 57 岁男性因 VS 接受 SRS 治疗,SRS 后肿瘤得到很好的控制。然而,在 SRS 后 9 年,他出现了蛛网膜下腔出血,并在肿瘤表面发现 SRS 诱导的远端前下小脑动脉动脉瘤。在夹闭手术中,动脉瘤嵌入肿瘤中,难以分离动脉瘤和肿瘤。此外,面神经和肿瘤限制了对母动脉的显露。只有通过切除肿瘤的尾部才能暴露靠近动脉瘤的母动脉近端。用永久夹夹闭动脉瘤,病理诊断为假性动脉瘤。

结论

提示 VS 相关的 SRS 诱导的假性动脉瘤与周围结构紧密粘连,由于肿瘤和面神经的存在,可能限制对母动脉的显露。在本病例报告中,我们详细描述了术中发现,这将有助于未来制定夹闭手术策略。

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