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睾丸和卵巢的混合型生殖细胞-性索间质肿瘤:比较与对比。

Mixed germ cell-sex cord stromal tumour of the testis and ovary: comparison and contrast.

机构信息

Department of Pathology and Laboratory Medicine, Indiana University School of Medicine, Indianapolis, IN, USA.

Department of Pathology and Laboratory Medicine, Indiana University School of Medicine, Indianapolis, IN, USA; Department of Urology, Indiana University School of Medicine, Indianapolis, IN, USA.

出版信息

Pathology. 2021 Feb;53(2):166-169. doi: 10.1016/j.pathol.2020.10.008. Epub 2020 Dec 25.

DOI:10.1016/j.pathol.2020.10.008
PMID:33358757
Abstract

Mixed germ cell-sex cord stromal tumours (MGC-SCSTs) of the testis and ovary differ significantly in their histological appearance, clinical behaviour, and molecular genetics. Until recently, the germ cells of testicular MGC-SCST were considered to be invariably histologically bland, whereas those from neoplasms that arise in the ovary have histological features characteristic of premalignancy. However, a recent histological and molecular genetic study demonstrated histological abnormalities and multiple chromosomal losses and gains in a small subset of testicular cases, thus providing the first evidence that testicular MGC-SCSTs can exceptionally show histological and molecular abnormalities. All cases of testicular MGC-SCST reported to date have been clinically benign, whereas ovarian examples are sometimes the precursor of a malignant germ cell neoplasm that can be clinically aggressive. Both genetic and epigenetic influences likely account for dissimilarities in these uncommon gonadal neoplasms.

摘要

睾丸和卵巢的混合性生殖细胞-性索间质肿瘤(MGC-SCST)在组织学表现、临床行为和分子遗传学上有显著差异。直到最近,人们一直认为睾丸 MGC-SCST 的生殖细胞在组织学上始终是温和的,而那些来源于卵巢的肿瘤具有癌前病变的特征。然而,最近的一项组织学和分子遗传学研究表明,一小部分睾丸病例存在组织学异常和多种染色体缺失和获得,这首次提供了证据表明睾丸 MGC-SCST 可能异常表现出组织学和分子异常。迄今为止报道的所有睾丸 MGC-SCST 病例均为临床良性,而卵巢病例有时是恶性生殖细胞瘤的前体,后者可能具有侵袭性的临床特征。遗传和表观遗传的影响可能解释了这些罕见性腺肿瘤的不同。

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