Wortsman J, Hughes L F
Department of Medicine, Southern Illinois University School of Medicine, Springfield, USA.
Am J Med Sci. 1996 Mar;311(3):135-8. doi: 10.1097/00000441-199603000-00005.
The olfactory and gonadal dysfunction in Kallmann syndrome share a common embryologic pathophysiology. To characterize further the linkage between the hypogonadotropic hypogonadism and anosmia, the authors performed a detailed evaluation of olfactory function in a patient with Kallman Syndrome having the rare variant of partial gonadotropin deficiency (fertile eunuch). The subject was seen initially at age 16 years because of delayed puberty. He received testosterone replacement therapy and subsequently completed pubertal development. As an adult, while untreated, he had subnormal levels of serum testosterone, low gonadotropins, and normal response to luteinizing hormone- releasing hormone. He also had impotence that was reversible with testosterone therapy, and a normal sperm count. Despite the mild degree of hypogonadism, olfactory function was completely absent, and the response to nasal trigeminal stimulants was markedly attenuated. Complete anosmia may therefore be associated with gonadotropin deficiency that is only partial; the presence of anosmia does not predict the need for gonadotropin therapy to attain fertility.
卡尔曼综合征中的嗅觉和性腺功能障碍有着共同的胚胎病理生理学机制。为了进一步明确低促性腺激素性性腺功能减退与嗅觉缺失之间的联系,作者对一名患有部分促性腺激素缺乏罕见变异型(可育宦官症)的卡尔曼综合征患者的嗅觉功能进行了详细评估。该患者最初因青春期延迟于16岁就诊。他接受了睾酮替代治疗,随后完成了青春期发育。成年后,在未接受治疗的情况下,他的血清睾酮水平低于正常,促性腺激素水平较低,对促黄体生成素释放激素的反应正常。他还患有阳痿,睾酮治疗后可逆转,精子计数正常。尽管性腺功能减退程度较轻,但嗅觉功能完全缺失,对鼻三叉神经刺激的反应明显减弱。因此,完全性嗅觉缺失可能与仅为部分性的促性腺激素缺乏有关;嗅觉缺失的存在并不能预测为实现生育而进行促性腺激素治疗的必要性。