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伴有融合和继发性启动子突变的甲状腺癌:一例报告及文献综述

Thyroid Carcinoma With Fusion and Secondary Promoter Mutation: A Case Report and Literature Review.

作者信息

Suh Ye Yoon, Hwang Yoon Jung, Bae Jung Mo, Koh Jiwon, Won Jae Kyung, Kim Sheehyun, Lee Sungyoung, Yun Hong Seok, Kim Su-Jin, Park Young Joo, Jung Kyung Cheon

机构信息

Department of Pathology, Seoul National University College of Medicine, Seoul, Republic of Korea.

Department of Genomic Medicine, Seoul National University Hospital, Seoul, Republic of Korea.

出版信息

Int J Surg Pathol. 2025 May;33(3):725-730. doi: 10.1177/10668969241271966. Epub 2024 Sep 16.

Abstract

Nuclear protein in testis (NUT) carcinoma is a rare but highly aggressive tumor characterized by translocation of the gene. To date, only about 20 NUT carcinomas arising from the thyroid have been reported in the literature, with the majority showing immunohistochemical markers indicative of squamous differentiation. We present a 29-year-old man with NUT carcinoma arising from thyroid follicular cells. Notably, the tumor cells expressed markers characteristic of thyroid follicular cells such as thyroglobulin, TTF1 and PAX8, without obvious histological and immunohistochemical features of squamous differentiation. Molecular analysis revealed a concurrent TERT promoter mutation (C228T) together with the fusion, a combination not previously documented in NUT carcinoma. The tumor highlights the need to include NUT carcinoma in the differential diagnosis of thyroid cancer, especially when it presents with unconventional histopathological features, even in the absence of signs of squamous differentiation.

摘要

睾丸核蛋白(NUT)癌是一种罕见但侵袭性很强的肿瘤,其特征是该基因发生易位。迄今为止,文献中仅报道了约20例起源于甲状腺的NUT癌,大多数病例显示出提示鳞状分化的免疫组化标志物。我们报告了一名29岁男性,其甲状腺滤泡细胞发生了NUT癌。值得注意的是,肿瘤细胞表达了甲状腺滤泡细胞的特征性标志物,如甲状腺球蛋白、TTF1和PAX8,而无明显的鳞状分化组织学和免疫组化特征。分子分析显示同时存在TERT启动子突变(C228T)以及融合,这种组合在NUT癌中以前未曾有过记录。该肿瘤凸显了在甲状腺癌鉴别诊断中纳入NUT癌的必要性,尤其是当它表现出非常规组织病理学特征时,即使没有鳞状分化迹象。

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