成人硬脑膜基础非典型畸胎瘤/横纹肌样肿瘤:DNA甲基化分析作为诊断工具。

Q1 Medicine CNS Oncology Pub Date : 2020-06-01 Epub Date: 2020-06-30 DOI:10.2217/cns-2020-0006
Hiba Alzoubi, Francesca Gianno, Felice Giangaspero, Daniela Bartolini, Luca Riccioni, Evelina Miele, Manila Antonelli
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引用次数: 3

摘要

非典型畸胎体/横纹肌样肿瘤(ATRT)是一种恶性中枢神经系统胚胎性肿瘤,多发生在儿童,成人病例罕见。我们报告一例23岁男性左额区轴外硬脑膜病变,先前诊断为胶质肉瘤。6年后,患者复发,回顾了以前的玻片。肿瘤vimentin阳性,INI1阴性。这种长生存的轴外肿瘤的鉴别诊断是横纹肌样脑膜瘤伴INI1缺失或ATRT。进行DNA甲基化分析以达到最终和最明确的诊断;结果是ATRT。我们的病例提示DNA甲基化谱在诊断挑战性中枢神经系统肿瘤方面的有用性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Dural-based atypical teratoid/rhabdoid tumor in an adult: DNA methylation profiling as a tool for the diagnosis.

Atypical teratoid/rhabdoid tumor (ATRT) is a malignant CNS embryonal tumor that mostly occurs in childhood, adult cases are rare. We report a case of a 23-year-old male with an extra-axial dura-based lesion in the left frontal area, previously diagnosed as gliosarcoma. After 6 years, the patient had a recurrence and the previous slides were reviewed. Tumor was positive for vimentin and negative for INI1. The differential diagnosis for this extra-axial tumor with long survival was rhabdoid meningioma with INI1 loss or ATRT. DNA methylation profiling was performed to reach the final and the most definitive diagnosis; the result was ATRT. Our case suggests the usefulness of DNA methylation profiling for diagnosing challenging CNS tumors.

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来源期刊
CNS Oncology
CNS Oncology Medicine-Neurology (clinical)
CiteScore
3.80
自引率
0.00%
发文量
12
审稿时长
13 weeks
期刊最新文献
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