一例成年患者,最初表现为桥小脑角黏液乳头状室管膜瘤:说明性病例。

Khatcher O Margossian, Marcin Marciniak, Akram Al-Warqi, Kenneth Aldape, Mehmet Kocak, Lorenzo Munoz, Elias Michaelides, Michael S Marshall
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引用次数: 0

摘要

背景:黏液乳头状室管膜瘤(MPEs)是一种相对罕见的室管膜瘤亚型,几乎只发生在腰骶棘的髓圆锥和终丝。颅内肿瘤的发生是罕见的,其中,定位到小脑桥脑角(CPA)是一个例外的事件。据作者所知,这是在CPA中报道的第5例MPE,在CPA中报道的第3例MPE。观察:作者描述了一位成年患者在CPA的初始表现为MPE,最初在放射成像上被认为是神经鞘瘤。随后的随访影像显示额外的临床无症状的脊柱肿块与MPEs一致。该病例特别独特,不仅因为患者的症状仅为耳鸣和耳胀,没有任何脊柱症状,而且因为据作者所知,这是第一例DNA甲基化分析结果被报道以确认CPA中MPE的诊断。经验教训:本病例强调了考虑CPA病变广泛鉴别诊断的重要性。https://thejns.org/doi/10.3171/CASE2586。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
An adult patient with initial presentation of myxopapillary ependymoma at the cerebellopontine angle: illustrative case.

Background: Myxopapillary ependymomas (MPEs) are a relatively rare subtype of ependymoma that occur almost exclusively at the conus medullaris and filum terminale in the lumbosacral spine. Intracranial occurrences of this tumor are rare, and of those, localization to the cerebellopontine angle (CPA) is an exceptional event. To the authors' knowledge, this is the fifthreported MPE in the CPA and only the third reported instance of an MPE in the CPA at the initial presentation.

Observations: The authors describe an adult patient with an initial presentation of MPE at the CPA, originally thought to be a schwannoma on radiological imaging. Follow-up imaging later revealed additional clinically asymptomatic spinal masses consistent with MPEs. This case is particularly unique not only because of the patient's presenting symptoms being exclusive to tinnitus and ear fullness without any spinal symptoms, but also because it is the first case, to the authors' knowledge, in which DNA methylation profiling results have been reported to confirm the diagnosis of MPE in the CPA.

Lessons: This case highlights the importance of considering a broad differential diagnosis for lesions in the CPA. https://thejns.org/doi/10.3171/CASE2586.

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