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骨内岩骨尖神经鞘瘤:病例报告及文献复习。

Intraosseous Petrous Apex Schwannoma: Case Report and Review of Literature.

机构信息

Department of Neurosurgery, NYU Langone Health, New York, New York, USA.

Department of Neurosurgery, NYU Langone Health, New York, New York, USA.

出版信息

World Neurosurg. 2019 Dec;132:182-187. doi: 10.1016/j.wneu.2019.08.157. Epub 2019 Aug 30.

DOI:10.1016/j.wneu.2019.08.157
PMID:31476472
Abstract

BACKGROUND

Intraosseous petrous apex schwannomas are an exceedingly rare entity; little is known about their epidemiology, natural history, and postoperative outcomes.

CASE DESCRIPTION

Here, we present the fourth known case of a primary intraosseous schwannoma of the petrous apex: a 68-year-old woman presenting with diplopia, facial numbness, progressive intermittent vertigo, tinnitus, diminished hearing, and ataxia. She underwent a transtemporal approach for subtotal resection of the tumor with subsequent stereotactic radiosurgery.

CONCLUSIONS

Our 2-year follow-up demonstrates slow growth and success of multimodal management in the treatment of these tumors. We review the 3 prior reports of petrous apex schwannomas and identify unifying radiographic and clinical characteristics to aid future diagnostic considerations of lesions of the petrous apex.

摘要

背景

骨内岩尖神经鞘瘤是一种非常罕见的实体瘤;关于其流行病学、自然病史和术后结果知之甚少。

病例描述

在这里,我们报告了第四例原发性骨内岩尖神经鞘瘤:一名 68 岁女性,表现为复视、面部麻木、进行性间歇性眩晕、耳鸣、听力下降和共济失调。她接受了经颞下入路行肿瘤次全切除术,随后行立体定向放射外科治疗。

结论

我们的 2 年随访显示,多模态治疗在这些肿瘤的治疗中取得了缓慢的进展和成功。我们回顾了之前 3 例岩尖神经鞘瘤的报告,并确定了统一的影像学和临床特征,以帮助未来对岩尖病变的诊断。

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