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Mixed germ cell-sex cord stromal tumour of the testis, further evidence supporting similarity of the germ cell component to spermatocytic tumour: case report.
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2
Fluorescence in-situ hybridization assessment of spindle cell-rich testicular sex cord stromal tumors demonstrates multiple chromosomal gains across histologic subtypes.荧光原位杂交评估富含梭形细胞的睾丸性索间质肿瘤显示多种组织学亚型的染色体获得。
Hum Pathol. 2024 Nov;153:105652. doi: 10.1016/j.humpath.2024.105652. Epub 2024 Aug 30.
3
Molecular characterization of large cell calcifying sertoli cell tumors: A multi-institutional study of 6 benign and 2 malignant tumors.大细胞钙化性支持细胞瘤的分子特征:一项对6例良性和2例恶性肿瘤的多机构研究。
Hum Pathol. 2024 Feb;144:15-21. doi: 10.1016/j.humpath.2023.12.008. Epub 2023 Dec 27.
4
Testicular Neoplasms With Sex Cord and Stromal Components Harbor a Recurrent Pattern of Chromosomal Gains.性索和间质成分的睾丸肿瘤具有染色体获得的复发性模式。
Mod Pathol. 2024 Jan;37(1):100368. doi: 10.1016/j.modpat.2023.100368. Epub 2023 Oct 21.
5
Germline APC Alterations May Predispose to Testicular Sex Cord-Stromal Tumors.胚系 APC 改变可能导致睾丸性索-间质肿瘤。
Am J Surg Pathol. 2023 Dec 1;47(12):1432-1437. doi: 10.1097/PAS.0000000000002132. Epub 2023 Oct 9.
6
Metastatic Testicular Sex Cord Tumor Harboring a Gene Fusion-A Case Report of a Novel Neoplasm: "Inflammatory and Nested Testicular Sex Cord Tumor".转移性睾丸性索肿瘤伴基因融合-一种新型肿瘤的病例报告:“炎症性和巢状睾丸性索肿瘤”。
Int J Surg Pathol. 2024 Jun;32(4):830-837. doi: 10.1177/10668969231195043. Epub 2023 Sep 16.
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Juvenile granulosa cell tumor in an adult woman during pregnancy: A case report and review of the literature.成年女性孕期的青少年型颗粒细胞瘤:一例病例报告及文献复习
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Large cell calcifying Sertoli cell tumour: molecular and immunohistochemical assessment of a series comprising non-metastasising and metastasising neoplasms.大细胞钙化性支持细胞瘤:一组非转移性和转移性肿瘤的分子及免疫组化评估
Histopathology. 2023 Jun;82(7):1079-1088. doi: 10.1111/his.14895. Epub 2023 Mar 16.
9
Molecular Correlates of Aggressive Behavior and Biological Progression in Testicular Sertoli Cell Tumors.睾丸支持细胞瘤侵袭性行为和生物学进展的分子相关性。
Mod Pathol. 2023 Jul;36(7):100152. doi: 10.1016/j.modpat.2023.100152. Epub 2023 Mar 10.
10
Testicular Juvenile Granulosa Cell Tumors Demonstrate Recurrent Loss of Chromosome 10 and Absence of Molecular Alterations Described in Ovarian Counterparts.睾丸幼年型颗粒细胞瘤表现为常染色体 10 的反复缺失,且不存在卵巢对应物中描述的分子改变。
Mod Pathol. 2023 Jun;36(6):100142. doi: 10.1016/j.modpat.2023.100142. Epub 2023 Feb 20.

睾丸性索间质肿瘤的评估与分类:来自泌尿生殖病理学会(GUPS)和国际泌尿病理学会(ISUP)专家小组——睾丸性索间质肿瘤(TESST)组的建议

Assessment and classification of sex cord-stromal tumours of the testis: recommendations from the testicular sex cord-stromal tumour (TESST) group, an Expert Panel of the Genitourinary Pathology Society (GUPS) and International Society of Urological Pathology (ISUP).

作者信息

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

机构信息

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.

出版信息

Histopathology. 2025 Nov;87(5):660-676. doi: 10.1111/his.15482. Epub 2025 Jun 18.

DOI:
10.1111/his.15482
PMID:40528632
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12522033/
Abstract

AIMS

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.

METHODS AND RESULTS

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.

CONCLUSIONS

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).

摘要

目的

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。

方法与结果

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。

结论

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。