Johnson R E, Scheithauer B
Am J Clin Pathol. 1982 Apr;77(4):501-7. doi: 10.1093/ajcp/77.4.501.
The case of a 23-year-old man with Nelson's syndrome is presented. He had undergone bilateral adrenalectomy at age 15 years for Cushing's syndrome. Postoperatively, his cushingoid features resolved; however, 13 months later, he became hyperpigmented and showed radiographic evidence of sellar enlargement and midline expansion of the sellar floor. In 1972, he received radiation therapy to the pituitary gland. He underwent transsphenoidal hypophysectomy in 1974 and 1975 for recurrent pituitary adenoma, and recurrent Cushing's syndrome developed concomitantly with bilateral firm testicular masses in 1978. External scanning with NP-59 localized steroid production to the testes, and bilateral orchiectomy was performed. Immunohistochemical studies of the pituitary tumor confirmed the presence of adrenocorticotropic hormone, and morphologic and ultrastructural examinations of the testes supported the adrenal nature of the testicular tumors.
本文报告了一例23岁患有尼尔森综合征的男性病例。他15岁时因库欣综合征接受了双侧肾上腺切除术。术后,他的库欣样特征消失;然而,13个月后,他出现色素沉着,并显示出蝶鞍增大及蝶鞍底部中线扩展的影像学证据。1972年,他接受了垂体放射治疗。1974年和1975年,他因复发性垂体腺瘤接受了经蝶窦垂体切除术,1978年复发性库欣综合征伴双侧坚实睾丸肿块出现。用NP - 59进行的外部扫描将类固醇生成定位到睾丸,随后进行了双侧睾丸切除术。垂体肿瘤的免疫组织化学研究证实了促肾上腺皮质激素的存在,睾丸的形态学和超微结构检查支持睾丸肿瘤的肾上腺性质。