扩展 NUTM1 重排肉瘤的范围:8例临床病理学和分子遗传学研究。

IF 4.5 1区 医学 Q1 PATHOLOGY
American Journal of Surgical Pathology Pub Date : 2024-08-01 Epub Date: 2024-07-01 DOI:10.1097/PAS.0000000000002254
Peipei Zhu, Ke Sun, I Weng Lao, Lin Yu, Qianming Bai, Xiaoyan Zhou, Jian Wang
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引用次数: 0

摘要

除了致命的中线癌(NUT 癌)外,间质瘤中也有 NUTM1 易位的报道,但极为罕见。在这里,我们描述了一系列 8 例 NUTM1 重排肉瘤,以进一步描述这一新兴实体的临床病理特征。这组患者包括 2 名男性和 6 名女性,年龄在 24 岁至 64 岁之间(平均:51 岁;中位数:56 岁)。肿瘤发生在结肠(2 例)、腹部(2 例)、空肠(1 例)、食道(1 例)、肺部(1 例)和眶下区(1 例)。确诊时,6 名患者出现转移性疾病。肿瘤大小从 1 厘米到 10.5 厘米不等(平均:6 厘米;中位数:5.5 厘米)。组织学上,4 个肿瘤由原始的小圆细胞到上皮样细胞组成,其中夹杂着可变的纺锤形细胞,3 个肿瘤完全由小圆细胞到上皮样细胞组成,1 个肿瘤主要由高级别纺锤形细胞组成。肿瘤细胞呈实性片状、巢状或交错束状排列。有丝分裂活性从1到15/10 HPF不等(中位数:5/10 HPF)。其他特征包括横纹肌表型(4/8)、明显的核卷曲(2/8)、突出的基质透明化(2/8)、局部肌样基质(1/8)、破骨细胞灶(1/8)和坏死(1/8)。通过免疫组化,所有肿瘤均显示 NUT 蛋白的弥漫性强核染色,同时泛影角蛋白(AE1/AE3)(2/8)、CK18(1/8)、CD99(3/8)、NKX2.2(2/8)、细胞周期蛋白 D1(2/8)、desmin(2/8)、BCOR(2/8)、S100(1/8)、TLE1(1/8)和突触素(1/8)也有不同程度的表达。通过荧光原位杂交分析,8 例肿瘤中有 7 例显示出 NUTM1 重排。RNA测序分析分别发现了MXD4::NUTM1(3/7)、MXI1::NUTM1(3/7)和MGA::NUTM1(1/7)融合。2例患者的DNA甲基化图谱显示,其甲基化群与NUT癌、未分化小圆形细胞肉瘤和纺锤形细胞肉瘤的甲基化群不同。随访期间(4至24个月),1名患者在8.5个月时复发,4名患者存活并有转移病灶(确诊后5、10、11和24个月),3名患者状况良好,无复发或转移迹象(确诊后4、6和12个月)。我们的研究进一步表明,NUTM1 重组肉瘤的临床病理范围很广。对于传统方法难以分类的单发未分化小圆形、上皮样至高级别纺锤形细胞恶性肿瘤,NUT免疫组化应纳入诊断方法。基于DNA的甲基化分析可能会为未分化肉瘤的表观遗传学分类提供一种有前途的工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Expanding the Spectrum of NUTM1 -Rearranged Sarcoma : A Clinicopathologic and Molecular Genetic Study of 8 Cases.

Apart from the lethal midline carcinoma (NUT carcinoma), NUTM1 translocation has also been reported in mesenchymal tumors, but is exceedingly rare. Here, we describe a series of 8 NUTM1 -rearranged sarcomas to further characterize the clinicopathologic features of this emerging entity. This cohort included 2 males and 6 females with age ranging from 24 to 64 years (mean: 51 y; median: 56 y). Tumors occurred in the colon (2), abdomen (2), jejunum (1), esophagus (1), lung (1) and infraorbital region (1). At diagnosis, 6 patients presented with metastatic disease. Tumor size ranged from 1 to 10.5 cm (mean: 6 cm; median: 5.5 cm). Histologically, 4 tumors were composed of primitive small round cells to epithelioid cells intermixed with variable spindle cells, while 3 tumors consisted exclusively of small round cells to epithelioid cells and 1 tumor consisted predominantly of high-grade spindle cells. The neoplastic cells were arranged in solid sheets, nests, or intersecting fascicles. Mitotic activity ranged from 1 to 15/10 HPF (median: 5/10 HPF). Other features included rhabdoid phenotype (4/8), pronounced nuclear convolutions (2/8), prominent stromal hyalinization (2/8), focally myxoid stroma (1/8), foci of osteoclasts (1/8), and necrosis (1/8). By immunohistochemistry, all tumors showed diffuse and strong nuclear staining of NUT protein, with variable expression of pancytokeratin (AE1/AE3) (2/8), CK18 (1/8), CD99 (3/8), NKX2.2 (2/8), cyclin D1 (2/8), desmin (2/8), BCOR (2/8), S100 (1/8), TLE1 (1/8), and synaptophysin (1/8). Seven of 8 tumors demonstrated NUTM1 rearrangement by fluorescence in situ hybridization analysis. RNA-sequencing analysis identified MXD4::NUTM1 (3/7), MXI1::NUTM1 (3/7), and MGA::NUTM1 (1/7) fusions, respectively. DNA-based methylation profiling performed in 2 cases revealed distinct methylation cluster differing from those of NUT carcinoma and undifferentiated small round cell and spindle cell sarcomas. At follow-up (range: 4 to 24 mo), 1 patient experienced recurrence at 8.5 months, 4 patients were alive with metastatic disease (5, 10, 11, and 24 mo after diagnosis), 3 patients remained well with no signs of recurrence or metastasis (4, 6, and 12 mo after diagnosis). Our study further demonstrated that NUTM1 -rearranged sarcoma had a broad range of clinicopathologic spectrum. NUT immunohistochemistry should be included in the diagnostic approach of monotonous undifferentiated small round, epithelioid to high-grade spindle cell malignancies that difficult to classify by conventional means. DNA-based methylation profiling might provide a promising tool in the epigenetic classification of undifferentiated sarcomas.

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来源期刊
CiteScore
10.30
自引率
5.40%
发文量
295
审稿时长
1 months
期刊介绍: The American Journal of Surgical Pathology has achieved worldwide recognition for its outstanding coverage of the state of the art in human surgical pathology. In each monthly issue, experts present original articles, review articles, detailed case reports, and special features, enhanced by superb illustrations. Coverage encompasses technical methods, diagnostic aids, and frozen-section diagnosis, in addition to detailed pathologic studies of a wide range of disease entities. Official Journal of The Arthur Purdy Stout Society of Surgical Pathologists and The Gastrointestinal Pathology Society.
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