Université Paris-Sud, Le Kremlin-Bicêtre, France.
Ann Endocrinol (Paris). 2012 Apr;73(2):141-6. doi: 10.1016/j.ando.2012.03.040. Epub 2012 Apr 25.
Acquired hypogonadotropic hypogonadism (AHH), contrary to congenital hypogonadotropic hypogonadism (CHH) is characterized by postnatal onset of disorders that damage or alter the function of gonadotropin-releasing hormone (GnRH) neurons and/or pituitary gonadotroph cells. AHH thus prevents the establishment of gonadotropin secretion at puberty, or its post-pubertal maintenance. Thus, postnatal AHH may prevent the onset of puberty or appear during pubertal development, but it usually emerges after the normal age of puberty. Although pituitary tumors, particularly prolactinoma, are the most common cause, sellar tumors or cyst of the hypothalamus or infundibulum, infiltrative, vascular, iron overload and other disorders may also cause AHH. Pituitary surgery and head trauma or cranial/pituitary radiation therapy are also usual causes of AHH. The clinical manifestations of AHH depend on age of onset, the degree of gonadotropin deficiency, the rapidity of its onset and the association to other pituitary function deficiencies or excess. Men with AHH have less stamina, decreased libido, erectile dysfunction and strength, and a worsened sense of well being leading to degraded quality of life. The physical examination is usually normal if hypogonadism is of recent onset. Diminished facial, body hair and muscle mass, fine facial wrinkles, gynecomastia, and hypotrophic testes are observed in long-standing and complete AHH. Spermatogenesis is impaired and the volume of ejaculate is decreased only when gonadotropins and testosterone levels are very low. Men with AHH may have normal or low serum LH and FSH concentrations, but normal gonadotropin values are inappropriate when associated with low serum testosterone. In the majority of AHH patients, serum inhibin B is "normal". The decrease of this sertolian hormone indicates a long-standing and severe gonadotropin deficiency. Symptoms, usually associated with significant testosterone deficiency in men with AHH, improve with testosterone replacement therapy. Replacement therapy is often simple, using an injectable testosterone ester as first line treatment. Fertility can be restored rather quickly, provided there is no independent primary testicular damage and the partner is fertile.
获得性促性腺激素低下性性腺功能减退症(AHH)与先天性促性腺激素低下性性腺功能减退症(CHH)相反,其特征是产后出现破坏或改变促性腺激素释放激素(GnRH)神经元和/或垂体促性腺细胞功能的疾病。因此,AHH 可防止青春期时促性腺激素的分泌建立,或其青春期后的维持。因此,产后 AHH 可能会阻止青春期的开始,或在青春期发育期间出现,但通常在正常青春期年龄后出现。虽然垂体肿瘤,特别是催乳素瘤,是最常见的原因,但鞍内肿瘤或下丘脑或漏斗囊肿、浸润性、血管性、铁过载和其他疾病也可能导致 AHH。垂体手术、头部外伤或颅/垂体放射治疗也是 AHH 的常见原因。AHH 的临床表现取决于发病年龄、促性腺激素缺乏程度、发病的迅速性以及与其他垂体功能减退或亢进的相关性。AHH 男性的耐力降低、性欲降低、勃起功能障碍和力量减弱,以及幸福感恶化,导致生活质量下降。如果性腺功能减退症是新近发生的,体格检查通常正常。长期和完全性 AHH 患者可见面部、体毛和肌肉减少、细小面部皱纹、男性乳房发育症和睾丸萎缩。当促性腺激素和睾酮水平非常低时,精子发生受损,精液量减少。AHH 男性的血清 LH 和 FSH 浓度可能正常或降低,但当与血清睾酮降低相关时,正常的促性腺激素值是不适当的。在大多数 AHH 患者中,血清抑制素 B“正常”。这种 sertolian 激素的减少表明长期和严重的促性腺激素缺乏。与 AHH 男性严重睾酮缺乏相关的症状通常在接受睾酮替代治疗后得到改善。替代治疗通常很简单,使用注射用睾酮酯作为一线治疗。只要没有独立的原发性睾丸损伤且伴侣具有生育能力,生育能力就能很快恢复。