Department of Nephro-urology, Nagoya City University Graduate School of Medical Sciences, Nagoya, Aichi, Japan.
Urology. 2012 Mar;79(3):684-6. doi: 10.1016/j.urology.2011.10.032. Epub 2011 Dec 14.
Kallmann syndrome (KS) is a genetic disorder characterized by the simultaneous occurrence of idiopathic hypogonadotropic hypogonadism (IHH) and anosmia. Here, we present 3 cases of KS with detailed description. In Case 1, testicular morphology was examined by testicular biopsy, and Leydig cells were examined by immunohistochemistry using antibodies against Ad4BP/SF1. Contrary to our predictions, the present study revealed the presence of Leydig cells in the testis. Testicular morphology in the patients with KS is more varied than expected, and further investigation is required to elucidate hormonal effects on normal testicular development.
卡尔曼综合征(KS)是一种遗传性疾病,其特征是同时发生特发性促性腺激素低下性性腺功能减退症(IHH)和嗅觉缺失。在这里,我们详细描述了 3 例 KS 病例。在病例 1 中,通过睾丸活检检查睾丸形态,并用针对 Ad4BP/SF1 的抗体通过免疫组织化学检查间质细胞。与我们的预测相反,本研究显示睾丸中存在间质细胞。KS 患者的睾丸形态比预期的更为多样化,需要进一步研究阐明激素对正常睾丸发育的影响。