Perivascular Epithelioid Cell Tumor of the Lung With a Novel YAP1::TFE3 Fusion.

IF 1 4区 医学 Q4 PATHOLOGY
William MacDonald, Matthew R Avenarius, Jenna Aziz, Aaron Guo, Desmond M D'Souza, Swati Satturwar, Konstantin Shilo
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引用次数: 0

Abstract

Perivascular epithelioid cell tumor (PEComa) belongs to a family of rare mesenchymal neoplasms that share characteristic morphologic, immunohistochemical and molecular findings. In this report, we provide a detailed clinicopathological characterization of a PEComa incidentally discovered in the right lung of a 53-year-old woman. This tumor with epithelioid cell morphology and myomelanocytic differentiation demonstrated a TFE3::YAP1 fusion by targeted RNA sequencing. While a subset of PEComas shows TFE3 rearrangements, fusion with YAP1 has not been systematically documented in this entity. Clear cell stromal tumor of the lung and epithelioid hemangioendothelioma characteristically display the TFE3::YAP1 fusion; however, as currently defined, both lack myomelanocytic features. Here, we describe a novel TFE3 fusion partner that further expands the spectrum of molecular alterations seen in PEComa.

新型 YAP1::TFE3 融合的肺血管周围上皮样细胞瘤
血管周围上皮样细胞瘤(PEComa)属于罕见的间叶肿瘤家族,它们在形态学、免疫组织化学和分子研究方面都有共同的特征。在本报告中,我们提供了一名 53 岁女性右肺中偶然发现的 PEComa 的详细临床病理特征。该肿瘤具有上皮样细胞形态和骨髓细胞分化,通过靶向 RNA 测序显示出 TFE3::YAP1 融合。虽然有一部分 PEComas 会出现 TFE3 重排,但该肿瘤与 YAP1 的融合还没有系统的记录。肺透明细胞间质瘤和上皮样血管内皮细胞瘤具有TFE3::YAP1融合的特征;然而,根据目前的定义,这两种肿瘤都缺乏骨髓细胞特征。在这里,我们描述了一种新型 TFE3 融合伙伴,它进一步扩展了 PEComa 的分子改变范围。
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来源期刊
CiteScore
2.10
自引率
0.00%
发文量
198
审稿时长
1 months
期刊介绍: International Journal of Surgical Pathology (IJSP) is a peer-reviewed journal published eight times a year, which offers original research and observations covering all major organ systems, timely reviews of new techniques and procedures, discussions of controversies in surgical pathology, case reports, and images in pathology. This journal is a member of the Committee on Publication Ethics (COPE).
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