Department of Pathology and Laboratory Medicine, Indiana University School of Medicine, Clarian Pathology Laboratory, Indianapolis, IN, USA.
Am J Surg Pathol. 2010 Dec;34(12):1874-80. doi: 10.1097/PAS.0b013e3181fcab70.
Sertoli cell nodules are almost always incidental microscopic lesions found in both cryptorchid and normally descended testes. Sertoli cell nodules, when present as masses or ultrasonographic lesions, may create diagnostic confusion. Herein, we report 6 cases of macroscopic Sertoli cell nodules that were received in consultation. The referral diagnoses included Sertoli cell tumor (2 cases), sex cord tumor with annular tubules (1 case), and gonadoblastoma (1 case). The patients were 19 to 36 years old: 3 patients presented with palpable testicular masses and 3 with lesions that were worrisome for neoplasms in ultrasonographic examinations conducted for pain (2 cases) or infertility (1 case). All were phenotypically normal male patients who lacked endocrine symptoms. The Sertoli cell nodules ranged from 6 to 10 mm in diameter and on microscopic examination consisted of circumscribed proliferations of immature Sertoli cells, globules and trabeculae of basement membrane, and spermatogonia in varying proportions. In 2 cases the lesion was distinctly intratubular, consisting of closely packed tubules containing various components; in the other cases there was confluent growth of the tubules. Immunostains for α-inhibin highlighted the Sertoli cells (5 of 5 cases), with the germ cells appearing in negative relief. An antibody for testis-specific protein, Y-encoded (TSPY), stained the spermatogonia (2 of 2 cases), whereas OCT 3/4 was negative in all the cases (5 of 5 cases). We conclude that Sertoli cell nodules may present clinically as mass lesions, and that it is important to distinguish them from true neoplasms to avoid unnecessary procedures.
支持细胞结节几乎总是在隐睾和正常下降的睾丸中偶然发现的显微镜下病变。支持细胞结节,当作为肿块或超声病变存在时,可能会造成诊断上的混淆。在此,我们报告 6 例经咨询收到的宏观支持细胞结节。转诊诊断包括支持细胞瘤(2 例)、环状管状性索肿瘤(1 例)和卵睾瘤(1 例)。患者年龄为 19 至 36 岁:3 例出现可触及的睾丸肿块,3 例超声检查发现可疑肿瘤病变(2 例)或不育(1 例)。所有患者均为表型正常的男性,无内分泌症状。支持细胞结节直径 6 至 10 毫米,镜下由不成熟支持细胞、基底膜的小球和小梁以及精原细胞以不同比例的局限性增生组成。在 2 例中,病变明显为管内型,由含有各种成分的紧密堆积小管组成;在其他病例中,小管呈融合性生长。α-抑制素免疫染色突出了支持细胞(5 例中的 5 例),生殖细胞呈阴性反应。睾丸特异性蛋白 Y 编码(TSPY)抗体染色精原细胞(2 例中的 2 例),而 OCT 3/4 在所有病例中均为阴性(5 例中的 5 例)。我们得出结论,支持细胞结节在临床上可能表现为肿块病变,重要的是要将其与真正的肿瘤区分开来,以避免不必要的程序。