Deng Y, Osamura Y, Tanaka M, Katsuoka Y, Kawamura N, Murakoshi M
Department of Pathology, School of Medicine, Tokai University, Isehara, Japan.
Acta Pathol Jpn. 1990 Jan;40(1):67-72. doi: 10.1111/j.1440-1827.1990.tb01531.x.
Testosterone-secreting adrenal adenoma is rare. We recently experienced a 17-year-old pubertal girl who showed signs of virilization and a high serum level of testosterone. The excised adrenal gland showed a 3.5 x 3 x 3-cm cortical adenoma. Light and electron microscopic findings together with the high serum level and high tumor tissue contents of testosterone and dehydroepiandrosterone (DHA) indicated that the tumor was a testosterone-secreting adrenal cortical adenoma. This appears to be a rather rare tumor from a review of the literature. Interestingly, in this case, the cytoplasm of the tumor cells contained structures resembling spironolactone bodies. From the results of enzyme histochemistry, the steroidogenetic pathways in this tumor were speculated.
分泌睾酮的肾上腺腺瘤很罕见。我们最近接诊了一名17岁的青春期女孩,她出现了男性化体征且血清睾酮水平升高。切除的肾上腺显示有一个3.5×3×3厘米的皮质腺瘤。光镜和电镜检查结果,以及血清高水平和肿瘤组织中高含量的睾酮和脱氢表雄酮(DHA)表明,该肿瘤是分泌睾酮的肾上腺皮质腺瘤。从文献回顾来看,这似乎是一种相当罕见的肿瘤。有趣的是,在这个病例中,肿瘤细胞的细胞质中含有类似螺内酯体的结构。根据酶组织化学的结果,推测了该肿瘤的类固醇生成途径。