ERBB2/ERBB3突变的S100/SOX10阳性未分类高级别子宫肉瘤:首次详细描述一种新型实体。

IF 3.4 3区 医学 Q1 PATHOLOGY
Abbas Agaimy, Josephine K Dermawan, Florian Haller, Sabine Semrau, Norbert Meidenbauer, Robert Stoehr, Sigurd Lax, Arndt Hartmann, Ying S Zou, Deyin Xing, Lars Tögel, John M Gross, Michael Michal
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引用次数: 0

摘要

随着创新型新一代测序(NGS)平台在常规诊断和研究中的应用日益广泛,子宫肉瘤的基因状况在过去二十年中也在不断发生变化。值得注意的是,最近发现的子宫肉瘤基因型大多为基因融合型,而具有诊断和/或治疗价值的复发性癌基因突变却很少见。最近,一种表达 S100 和 SOX10,但缺乏其他子宫恶性肿瘤的诊断形态学、免疫表型和分子特征的独特侵袭性子宫肉瘤以科学摘要的形式发表(USCAP,2023 年),但仍缺乏对该实体的详细描述和划分。我们在此描述了两种未分类的高级别子宫肉瘤,其特征为纺锤形至圆形细胞形态以及 S100 和 SOX10 的弥漫表达,分别起源于 53 岁和 45 岁女性的子宫体和宫颈,并分别携带 ERBB3(p.Glu928Gly)和 ERBB2(p.Val777Leu)突变。此外,这两种肿瘤都存在基因组 HER2 扩增、ATRX 突变和 CDKN2A 缺失。甲基化研究显示其甲基组与 MPNST 样肿瘤最相似,但与黑色素瘤、MPNST、透明细胞肉瘤和子宫内膜间质肉瘤不同。病例 1 在确诊 47 个月后,经多次化疗后死于进展性腹膜转移。病例 2 是最近的一个病例,患者出现宫颈肿块并进行了活组织检查。本研究确定了一种新的迄今未被发现的侵袭性子宫肉瘤,具有独特的表型和基因型特征。鉴于靶向 HER2 的潜在价值,认识这种肿瘤类型对于制定适当的治疗策略和将来更好地界定该实体至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

ERBB2/ ERBB3-mutated S100/ SOX10-positive unclassified high-grade uterine sarcoma: first detailed description of a novel entity.

ERBB2/ ERBB3-mutated S100/ SOX10-positive unclassified high-grade uterine sarcoma: first detailed description of a novel entity.

With the increasing use of innovative next generation sequencing (NGS) platforms in routine diagnostic and research settings, the genetic landscape of uterine sarcomas has been dynamically evolving during the last two decades. Notably, the majority of recently recognized genotypes in uterine sarcomas represent gene fusions, while recurrent oncogene mutations of diagnostic and/ or therapeutic value have been rare. Recently, a distinctive aggressive uterine sarcoma expressing S100 and SOX10, but otherwise lacking diagnostic morphological, immunophenotypic and molecular features of other uterine malignancies has been presented in a scientific abstract form (USCAP, 2023), but detailed description and delineation of the entity is still missing. We herein describe two high-grade unclassified uterine sarcomas characterized by spindle to round cell morphology and diffuse expression of S100 and SOX10, originating in the uterine body and cervix of 53- and 45-year-old women and carrying an ERBB3 (p.Glu928Gly) and an ERBB2 (p.Val777Leu) mutation, respectively. Both tumors harbored in addition genomic HER2 amplification, ATRX mutation and CDKN2A deletion. Methylation studies revealed a methylome most similar to MPNST-like tumors, but distinct from melanoma, MPNST, clear cell sarcoma, and endometrial stromal sarcoma. Case 1 died of progressive peritoneal metastases after multiple trials of chemotherapy 47 months after diagnosis. Case 2 is a recent case who presented with a cervical mass, which was biopsied. This study defines a novel heretofore unrecognized aggressive uterine sarcoma with unique phenotypic and genotypic features. Given the potential value of targeting HER2, recognizing this tumor type is mandatory for appropriate therapeutic strategies and for better future delineation of the entity.

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来源期刊
Virchows Archiv
Virchows Archiv 医学-病理学
CiteScore
7.40
自引率
2.90%
发文量
204
审稿时长
4-8 weeks
期刊介绍: Manuscripts of original studies reinforcing the evidence base of modern diagnostic pathology, using immunocytochemical, molecular and ultrastructural techniques, will be welcomed. In addition, papers on critical evaluation of diagnostic criteria but also broadsheets and guidelines with a solid evidence base will be considered. Consideration will also be given to reports of work in other fields relevant to the understanding of human pathology as well as manuscripts on the application of new methods and techniques in pathology. Submission of purely experimental articles is discouraged but manuscripts on experimental work applicable to diagnostic pathology are welcomed. Biomarker studies are welcomed but need to abide by strict rules (e.g. REMARK) of adequate sample size and relevant marker choice. Single marker studies on limited patient series without validated application will as a rule not be considered. Case reports will only be considered when they provide substantial new information with an impact on understanding disease or diagnostic practice.
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