双期肌上皮癌伴5p/5q缺失:一种新的涎腺肿瘤实体的形态分子特征和临时命名。

IF 4.2 1区 医学 Q1 PATHOLOGY
Philipp Jurmeister, Maximilian Leitheiser, Linda Bergmayr, Emma Payá Capilla, Liliana H Mochmann, Yauheniya Zhdanovich, Fabian Engelhardt-Schott, Konstanze Schleich, Doreen Klingler, Edgar Chimal, Cornelia M Focke, Gerben E Breimer, Ilse van Engen van Grunsven, Andreas von Deimling, David Capper, Frederick Klauschen, Stephan Ihrler
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引用次数: 0

摘要

唾液腺肿瘤的诊断具有挑战性,因为其良性和恶性肿瘤具有很大的多样性,具有巨大的肿瘤内和肿瘤间异质性,因此经常重叠的组织学特征。DNA甲基化极大地增强了几种器官的肿瘤分类,并导致了以前未被识别的实体的识别。在最近一项关于唾液腺肿瘤DNA甲基化的研究中,我们发现了一组无法分类的肿瘤。在这项研究中,我们通过临床、组织形态学、免疫组织化学和分子特征的综合分析来描述这一群体。这组12个肿瘤的特点是临床表现为良性的小肿瘤,女性占明显优势(91.7%),后者在其他唾液肿瘤类型中没有相似之处。除了独特的DNA甲基化谱外,拷贝数分析还揭示了染色体5p/5q的高复发性缺失和染色体12q上MDM2位点的频繁扩增。全外显子组和转录组测序未检测到复发性突变或融合。组织形态学特征只有中等程度的不同,包括专性的,因此可变的双相管状和单相肌上皮区域的混合,低或无核异型性,和最小的增殖。频繁的侵袭性行为,孤立的淋巴结转移,以及分子改变,共同强烈支持将其分类为低级别癌。总之,这些发现清楚地将该肿瘤组与组织形态学上相似的肿瘤实体区分开来,特别是肌上皮癌、上皮-肌上皮癌和腺样囊性癌。我们提出彻底的论点,这个肿瘤组代表一个独特的涎腺癌实体,而不是一个现有的变体。我们建议暂时命名为“双期肌上皮癌伴5p/5q损失”以供讨论。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Biphasic Myoepithelial Carcinoma With 5p/5q Loss: Morphomolecular Characterization and Provisional Designation of a Proposed Novel Salivary Tumor Entity.

Salivary gland tumors are diagnostically challenging due to major diversity of benign and malignant tumors with enormous intra-tumorous and inter-tumorous heterogeneity and, hence, frequently overlapping histologic features. DNA methylation has greatly enhanced tumor classification in several organs and led to the identification of previously unrecognized entities. In a recent study on DNA methylation of salivary gland tumors, we had identified a group of unclassifiable tumors. In this study, we characterize this group through an integrated analysis of clinical, histomorphologic, immunohistochemical, and molecular features. This group of 12 tumors is characterized by small, clinically benign appearing tumors with striking female predominance (91.7%), the latter not paralleled in other salivary tumor types. In addition to distinct DNA methylation profiling, copy number analysis revealed unique alterations with highly recurrent chromosome 5p/5q loss and frequent amplification of the MDM2 locus on chromosome 12q. Whole-exome and transcriptome sequencing detected no recurrent mutations or fusions. The histomorphologic features were only moderately distinct, comprising an obligate, thereby variable admixture of biphasic-tubular and monophasic-myoepithelial areas, low or absent nuclear atypia, and minimal proliferation. Frequent invasive behavior, a solitary lymph node metastasis, and the molecular alterations, altogether, strongly support classification as a, presumably low-grade, carcinoma. Altogether, these findings clearly distinguish this tumor group from histomorphologically similar tumor entities, in particular myoepithelial carcinoma, epithelial-myoepithelial carcinoma, and adenoid cystic carcinoma. We present thorough arguments that this tumor group represents a distinct salivary carcinoma entity rather than a variant of an existing one. We propose the provisional designation "Biphasic myoepithelial carcinoma with 5p/5q loss" for discussion.

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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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