Low-grade undifferentiated sarcoma with MEIS1::NCOA2-rearrangement primary to the lung: a case report

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS
Zachary Coty-Fattal, Bianca Carter, Michael J. Volek, Farres Obeidin
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引用次数: 0

Abstract

MEIS1::NCOA2 is a rare fusion gene that has been recently described in a subset of spindle cell rhabdomyosarcomas and multiple low-grade undifferentiated spindle cell sarcomas predominantly arising in the genitourinary and gynecologic tracts with no specific line of differentiation. We present the first documented case of this neoplasm arising as a lung primary tumor. A 74-year-old woman with a 40-year smoking history presented with a 2.1 × 1.7 cm lung nodule discovered on computed tomography (CT) scan. A biopsy and subsequent lobe resection were performed, as well as an extensive metastatic work up, which revealed no additional masses. No specific line of differentiation was found by immunohistochemical staining, and an RNA-based fusion panel revealed a MEIS1::NCOA2 fusion, at which point a diagnosis of Low-Grade Undifferentiated Sarcoma with MEIS1::NCOA2-Rearrangement was rendered. This report represents the first diagnosis of this tumor primary to the lung, and provides additional insight into the origin and localization of these rare tumors.
肺部原发 MEIS1::NCOA2 重排的低度未分化肉瘤:病例报告
MEIS1::NCOA2是一种罕见的融合基因,最近在一部分纺锤细胞横纹肌肉瘤和多种低度未分化纺锤细胞肉瘤中得到了描述,这些肿瘤主要发生在泌尿生殖道和妇科,没有特定的分化线。我们介绍了第一例有记录的肺原发肿瘤病例。一名有 40 年吸烟史的 74 岁女性在接受计算机断层扫描(CT)时发现了一个 2.1 × 1.7 厘米的肺部结节。随后进行了活组织检查和肺叶切除术,并进行了广泛的转移检查,结果没有发现其他肿块。免疫组化染色未发现特异性分化线,基于 RNA 的融合检测显示 MEIS1::NCOA2 融合,诊断为 MEIS1::NCOA2 后向排列的低分化肉瘤。该报告是首次诊断出这种原发于肺部的肿瘤,并对这种罕见肿瘤的起源和定位提供了更多的见解。
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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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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