Novel case of ependymoma-like tumor with mesenchymal differentiation harboring ZFTA::RELA fusion in an adult.

IF 2.7 3区 医学 Q2 CLINICAL NEUROLOGY Brain Tumor Pathology Pub Date : 2024-10-01 Epub Date: 2024-09-08 DOI:10.1007/s10014-024-00489-6
Hirohisa Yajima, Shunsaku Takayanagi, Hirokazu Takami, Shota Tanaka, Masashi Nomura, Kaishi Satomi, Masako Ikemura, Sumihito Nobusawa, Ryuta Saito, Akihide Kondo, Nobuhito Saito
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Abstract

High-grade supratentorial tumors harboring ZFTA::NCOA1/2 fusion in infants presenting with mixed histology of embryonal-appearing components resembling ependymoma and mesenchymal sarcomatous components have recently been reported as ependymoma-like tumors with mesenchymal differentiation (ELTMDs). In contrast, we describe herein a pathologically similar case with a novel ZFTA::RELA fusion in an adult. A frontal lobe lesion was resected from a 30-year-old woman and displayed mixed components on pathological examination, showing ependymoma-like and sarcomatous parts. The absence of perivascular pseudorosettes was inconsistent with a diagnosis of ependymoma. Fluorescence in situ hybridization analysis confirmed ZFTA::RELA fusion. The DKFZ methylation classifier (v12.8) did not categorize this case among established methylation classes. In addition, t-distributed stochastic neighbor embedding analysis using DNA methylation data revealed that the present case was distant from ependymomas but close to two previously reported cases of ELTMD involving ZFTA::NCOA1/2 fusion. Taken together, we concluded that this tumor should be considered under the entity of ELTMD. This represents the first description of an adult patient with ELTMD harboring ZFTA::RELA fusion analyzed by DNA methylation profiling, supporting the establishment of ELTMD as a possible new tumor type.

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成人间充质分化的附睾瘤样肿瘤新病例,携带 ZFTA::RELA 融合基因。
最近有报道称,婴儿颅上高级别肿瘤中含有ZFTA::NCOA1/2融合,其组织学表现为胚胎样成分与间质肉瘤成分的混合组织学,与间质分化的肾上腺皮质瘤样肿瘤(ELTMDs)相似。相比之下,我们在此描述了一例病理上类似的成人新型ZFTA::RELA融合病例。一名30岁女性的额叶病变被切除,病理检查显示病变成分混杂,既有附骨瘤样部分,也有肉瘤样部分。血管周围没有假包膜,这与上皮瘤的诊断不符。荧光原位杂交分析证实了 ZFTA::RELA 融合。DKFZ 甲基化分类器(v12.8)没有将该病例归入既定的甲基化类别。此外,利用DNA甲基化数据进行的t分布随机相邻嵌入分析显示,本病例与脑外胶质瘤相距甚远,但与之前报道的两例涉及ZFTA::NCOA1/2融合的ELTMD病例相近。综上所述,我们认为该肿瘤应归入ELTMD。这是通过DNA甲基化图谱分析首次描述携带ZFTA::RELA融合的ELTMD成人患者,支持将ELTMD确立为一种可能的新肿瘤类型。
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来源期刊
Brain Tumor Pathology
Brain Tumor Pathology 医学-病理学
CiteScore
5.40
自引率
9.10%
发文量
30
审稿时长
>12 weeks
期刊介绍: Brain Tumor Pathology is the official journal of the Japan Society of Brain Tumor Pathology. This international journal documents the latest research and topical debate in all clinical and experimental fields relating to brain tumors, especially brain tumor pathology. The journal has been published since 1983 and has been recognized worldwide as a unique journal of high quality. The journal welcomes the submission of manuscripts from any country. Membership in the society is not a prerequisite for submission. The journal publishes original articles, case reports, rapid short communications, instructional lectures, review articles, letters to the editor, and topics.Review articles and Topics may be recommended at the annual meeting of the Japan Society of Brain Tumor Pathology. All contributions should be aimed at promoting international scientific collaboration.
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