TFE3型
血管周围上皮样细胞
上皮样血管内皮瘤
病理
融合基因
生物
免疫组织化学
肺
间充质干细胞
间质细胞
医学
上皮样细胞
内科学
基因
遗传学
基因表达
发起人
作者
William MacDonald,Matthew R. Avenarius,Jenna Aziz,Aaron Guo,Desmond M. D’Souza,Swati Satturwar,Konstantin Shilo
标识
DOI:10.1177/10668969251323936
摘要
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.
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