肉瘤
融合基因
病理
生物
肺
癌症研究
医学
基因
内科学
遗传学
作者
Natalia Georgantzoglou,Maryam Aghighi,Gregory M. Coté,Yin P. Hung,Darcy A. Kerr,Jason R. Pettus,Konstantinos Linos
标识
DOI:10.1177/10668969221092125
摘要
Originally described in a rare subset of poorly differentiated squamous cell carcinomas termed NUT carcinomas, NUTM1 rearrangements are now known to characterize a wide spectrum of neoplasms including sarcomas, poromas/porocarcinomas, unclassified adnexal carcinomas and pediatric acute lymphoblastic leukemia. The advent of next-generation sequencing (NGS) has led to the identification of a multitude of novel fusion partners in addition to BRD4, which was initially reported in the majority of NUT carcinomas. NUTM1-rearranged sarcomas usually harbor fusions with the MAD gene family ( MXD1, MXD4, MGA) and present as spindle cell proliferations in diverse locations in patients of all ages. Herein, we present a very rare case of spindle cell sarcoma of the lung, which harbored a NUTM1::MGA fusion and offer a comprehensive update of the recent data.
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