Roth Lawrence M, Cheng Liang
Department of Pathology, Indiana University School of Medicine, Indianapolis, Indiana, USA.
J Clin Pathol. 2017 Mar;70(3):222-227. doi: 10.1136/jclinpath-2016-203902. Epub 2016 Jul 25.
The origin of testicular mixed germ cell-sex cord stromal tumour (MGC-SCST) is uncertain, and the nature of this neoplasm is controversial. It has not been established whether the germ cells in testicular MGC-SCST are neoplastic or whether they are merely entrapped within an unclassified sex cord stromal tumour or related testicular neoplasm. In this investigation, we present additional evidence regarding the nature of the germ cells in testicular MGC-SCST.
We obtained 25 cases of MGC-SCST, 13 of which involved the testis and 12 occurred in the ovary for histological examination. Although the majority of the cases studied were archival, materials were available for immunocytochemical examination in 10 instances.
We found that 10 of 13 testicular MGC-SCSTs studied had a sex cord component resembling unclassified sex cord stromal tumour. In two MGC-SCSTs that had prominent entrapped tubules, an intratubular component was identified. A total of 12 ovarian MGC-SCSTs were examined, and these neoplasms were more diverse in their histological appearance than the testicular examples. The germ cells often resembled those of dysgerminoma. Formation of imperfect follicular-like structures was a frequent feature in ovarian cases.
In this investigation, we provide further evidence that the germ cells in testicular MGC-SCSTs are neoplastic; however, in the great majority of tumours, these cells are low-grade. Some testicular MGC-SCSTs arise from an intratubular component. We believe that the majority of ovarian and some testicular MGC-SCSTs arise more directly from simultaneous transformation of germ cells and sex cord derivatives.
睾丸混合性生殖细胞-性索间质肿瘤(MGC-SCST)的起源尚不确定,该肿瘤的性质存在争议。睾丸MGC-SCST中的生殖细胞是肿瘤性的,还是仅仅被困在未分类的性索间质肿瘤或相关睾丸肿瘤内,目前尚未明确。在本研究中,我们提供了关于睾丸MGC-SCST中生殖细胞性质的更多证据。
我们获取了25例MGC-SCST病例,其中13例累及睾丸,12例发生于卵巢,进行组织学检查。尽管所研究的大多数病例为存档病例,但有10例可用于免疫细胞化学检查。
我们发现,在研究的13例睾丸MGC-SCST中,有10例具有类似于未分类性索间质肿瘤的性索成分。在2例有明显被困小管的MGC-SCST中,识别出了管内成分。共检查了12例卵巢MGC-SCST,这些肿瘤的组织学表现比睾丸病例更多样化。生殖细胞常类似于无性细胞瘤中的生殖细胞。在卵巢病例中,形成不完全的滤泡样结构是常见特征。
在本研究中,我们提供了进一步的证据表明睾丸MGC-SCST中的生殖细胞是肿瘤性的;然而,在绝大多数肿瘤中,这些细胞为低级别。一些睾丸MGC-SCST起源于管内成分。我们认为,大多数卵巢和一些睾丸MGC-SCST更直接地起源于生殖细胞和性索衍生物的同时转化。