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起源于前庭神经的颅内古老型神经鞘瘤:一例报告并文献复习

Intracranial ancient schwannoma originating from vestibular nerve: A case report and review of the literature.

作者信息

Tsuchiya Takahiro, Miyawaki Satoru, Shinya Yuki, Teranishi Yu, Tomioka Arisa, Yamazawa Sho, Shin Masahito, Saito Nobuhito

机构信息

Department of Neurosurgery, Faculty of Medicine, The University of Tokyo, and.

Pathology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.

出版信息

Surg Neurol Int. 2022 Apr 15;13:143. doi: 10.25259/SNI_71_2022. eCollection 2022.

Abstract

BACKGROUND

Ancient schwannoma (AS) is a subtype of schwannoma with degenerative features, which often progresses slowly over a long period of time. Intracranial AS is a rare benign tumor and there are no detailed reports of AS originating from the vestibular nerve.

CASE DESCRIPTION

Herein, we present the case of a patient with the right vestibular schwannoma with multiple meningiomas and review three previous cases of intracranial AS. Near-total resection was performed for vestibular schwannoma and the pathological findings were AS (World Health Organization Grade I). Five months postoperatively, gamma knife radiosurgery was performed for a recurrent lesion of the right vestibular schwannoma in the internal auditory meatus. Although AS is known to be a benign pathology, there are cases of rapid growth and early recurrence, as the one presented here. The high Ki-67 index (up to 5%) and the presence of cysts may be related to the rapid progression of intracranial AS.

CONCLUSION

Therefore, careful follow-up is necessary even if adequate removal is achieved. In addition to pathological studies, the genetic background of intracranial AS warrants future investigations. Further accumulation of cases is necessary to clarify the clinical features of intracranial AS.

摘要

背景

古老型神经鞘瘤(AS)是神经鞘瘤的一种具有退行性特征的亚型,通常在很长一段时间内进展缓慢。颅内AS是一种罕见的良性肿瘤,目前尚无起源于前庭神经的AS的详细报道。

病例描述

在此,我们报告一例患有右侧前庭神经鞘瘤并伴有多发脑膜瘤的患者,并回顾之前三例颅内AS病例。对前庭神经鞘瘤进行了近全切除,病理结果为AS(世界卫生组织I级)。术后五个月,对内耳道内右侧前庭神经鞘瘤的复发灶进行了伽玛刀放射外科治疗。尽管已知AS是一种良性病变,但仍有生长迅速和早期复发的病例,如此处报告的这例。高Ki-67指数(高达5%)和囊肿的存在可能与颅内AS的快速进展有关。

结论

因此,即使实现了充分切除,也有必要进行仔细的随访。除了病理研究外,颅内AS的遗传背景值得未来进一步研究。需要进一步积累病例以阐明颅内AS的临床特征。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e390/9062893/0e85975de231/SNI-13-143-g001.jpg

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