Johnson C B, Gilbert E F, Gottlieb L I
South Med J. 1979 Mar;72(3):353-6. doi: 10.1097/00007611-197903000-00035.
We have described an unusual case of polyostotic fibrous dysplasia in a 25-year-old white woman who had malignant transformation into a mesenchymal tumor with widespread metastases and features of rhabdomyosarcoma. Masculinization also occurred with high plasma testosterone levels. A mechanism for the development of masculinizing features is discussed.
我们描述了一名25岁白人女性的罕见多骨型纤维发育不良病例,该病例发生了恶性转化,形成了具有广泛转移且具有横纹肌肉瘤特征的间充质肿瘤。同时还出现了男性化现象,血浆睾酮水平升高。本文讨论了男性化特征出现的机制。