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

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

机构信息

Institute of Pathology, Erlangen University Hospital, Friedrich Alexander University of Erlangen-Nuremberg, Erlangen, Germany.

Comprehensive Cancer Center, European Metropolitan Area Erlangen-Nuremberg (CCC ER-EMN), Erlangen, Germany.

出版信息

Virchows Arch. 2024 Nov;485(5):805-813. doi: 10.1007/s00428-024-03908-3. Epub 2024 Aug 28.

Abstract

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.

摘要

随着创新的下一代测序 (NGS) 平台在常规诊断和研究环境中的应用不断增加,子宫肉瘤的遗传景观在过去二十年中一直在动态演变。值得注意的是,子宫肉瘤中最近发现的大多数基因型代表基因融合,而具有诊断和/或治疗价值的反复致癌基因突变则很少见。最近,一种具有独特侵袭性的子宫肉瘤在科学摘要形式中被提出,其表达 S100 和 SOX10,但缺乏其他子宫恶性肿瘤的形态学、免疫表型和分子特征的诊断特征(USCAP,2023 年),但该实体的详细描述和划定仍然缺失。我们在此描述了两例高级别未分类的子宫肉瘤,其特征为梭形至圆形细胞形态和弥漫性表达 S100 和 SOX10,起源于 53 岁和 45 岁女性的子宫体和子宫颈,分别携带 ERBB3 (p.Glu928Gly) 和 ERBB2 (p.Val777Leu) 突变。两个肿瘤均存在基因组 HER2 扩增、ATRX 突变和 CDKN2A 缺失。甲基化研究表明,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 在诊断后 47 个月因多次化疗后进展性腹膜转移而死亡。病例 2 是最近的病例,表现为宫颈肿块,进行了活检。本研究定义了一种具有独特表型和基因型特征的新型迄今未被认识的侵袭性子宫肉瘤。鉴于靶向 HER2 的潜在价值,识别这种肿瘤类型对于适当的治疗策略和更好地定义该实体的未来是强制性的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0fd2/11564289/61c09146046c/428_2024_3908_Fig1_HTML.jpg

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