Pervaiz N, Hagedoorn J, Mininberg D T
Urology. 1979 Sep;14(3):267-9. doi: 10.1016/0090-4295(79)90498-9.
A patient with Kallman syndrome is presented emphasizing the urologic aspects of this unusual disorder. Testes biopsy at the time of orchiopexy demonstrated infantile testes with interstitial fibrosis and a diminished Leydig and Sertoli cell population. The electron micrograph confirmed type B Sertoli cells. The implications of these findings are discussed and details of treatment given.
本文介绍了一名卡尔曼综合征患者，着重强调了这种罕见疾病的泌尿外科方面情况。睾丸固定术时的睾丸活检显示睾丸呈婴儿型，伴有间质纤维化，睾丸间质细胞和支持细胞数量减少。电子显微镜检查证实为B型支持细胞。本文讨论了这些发现的意义并给出了治疗细节。
