Acosta Andres M, Colecchia Maurizio, Comperat Eva, Cornejo Kristine M, Gill Anthony J, Gupta Sounak, Cheville John C, Idrees Muhammad T, Kao Chia-Sui, Maclean Fiona, Matoso Andres, Raspollini Maria Rosaria, Michalova Kvetoslava, Reyes Múgica Miguel, Tickoo Satish K, Tsuzuki Toyonori, Ulbright Thomas M, Williamson Sean R, Siegmund Stephanie, Sholl Lynette M, Gonzalez-Peramato Pilar, Berney Daniel M
Department of Pathology and Laboratory Medicine, Indiana University School of Medicine and Indiana University Health Partners, Indianapolis, IN, USA.
Department of Pathology, Vita Salute San Raffaele University, Milan, Italy.
Histopathology. 2025 Nov;87(5):660-676. doi: 10.1111/his.15482. Epub 2025 Jun 18.
Testicular sex cord-stromal tumours (TSCSTs) are relatively rare, accounting for ~5% of all testicular neoplasms. They were historically classified into Leydig cell tumour, Sertoli cell tumour, granulosa cell tumour, and unclassified sex cord-stromal tumour. More recently, classification was expanded to incorporate additional histologic types, including some associated with inherited cancer predisposition syndromes. However, the classification of TSCSTs still relies entirely on morphology, with some tumour types being defined based on their resemblance to ovarian counterparts. In recent years, molecular studies have identified drivers and genomic alterations associated with aggressive behaviour and progression; however, these findings have not yet impacted classification and management.
Under sponsorship of the International Society of Urological Pathology (ISUP) and the Genitourinary Pathology Society (GUPS), a group of genitourinary pathologists was assembled in 2023 with the aim of assessing how to use these new data to improve the classification and management of TSCSTs.
This paper summarizes the recommendations derived from the consensus activities and the first meeting of the testicular sex cord-stromal tumour (TESST) group (held at Johns Hopkins Hospital, Baltimore, USA, 3/23/2024).
睾丸性索间质肿瘤(TSCSTs)相对罕见,约占所有睾丸肿瘤的5%。历史上,它们被分为间质细胞瘤、支持细胞瘤、颗粒细胞瘤和未分类的性索间质肿瘤。最近,分类范围有所扩大,纳入了更多组织学类型,包括一些与遗传性癌症易感性综合征相关的类型。然而,TSCSTs的分类仍然完全依赖形态学,一些肿瘤类型是根据它们与卵巢对应肿瘤的相似性来定义的。近年来,分子研究已经确定了与侵袭性行为和进展相关的驱动因素和基因组改变;然而,这些发现尚未影响分类和管理。
在国际泌尿病理学会(ISUP)和泌尿生殖病理学会(GUPS)的支持下,2023年召集了一组泌尿生殖病理学家,旨在评估如何利用这些新数据来改善TSCSTs的分类和管理。
本文总结了睾丸性索间质肿瘤(TESST)小组(于2024年3月23日在美国巴尔的摩约翰霍普金斯医院举行)的共识活动和首次会议得出的建议。