Fenichel Patrick
Service d'Endocrinologie et Médecine de la Reproduction, Centre Hospitalo-Universitaire de Nice, Hôpital de L'Archet, Nice, France.
Endocr Dev. 2012;22:138-159. doi: 10.1159/000326686. Epub 2012 Jul 25.
Since puberty is a long ongoing developmental process with significant individual and population differences in timing, the definition of delayed puberty for a given individual needs to rest on simple, though arbitrary criteria based on epidemiological data. Although several genes involved in the hypothalamic-pituitary-gonadal maturation cascade have been characterized recently from familial or sporadic cases of primitive isolated hypogonadotropic hypogonadism, many genes regulating puberty onset remain undetermined. In case of delayed puberty and/or primary amenorrhea, a complete clinical examination including a detailed past history will evaluate the development of secondary sex characteristics, verify the association with a growth delay and look for specific indicative features pertaining to the etiological diagnosis. This clinical check-up completed if necessary with biological, ultrasonographic, radiological and genetic investigations will try to determine which girls will have a permanent sexual infantilism of gonadal, hypophyseal or hypothalamic origin, which girls will undergo spontaneous but delayed puberty and which girls have primary amenorrhea with developed secondary sex characteristics. Therapeutic attitude will have to integrate etiological factors, statural prognosis, bone mass preservation and psychological factors.
由于青春期是一个长期持续的发育过程,在时间上存在显著的个体和群体差异,对于特定个体青春期延迟的定义需要基于简单但基于流行病学数据的任意标准。尽管最近从家族性或散发性原发性孤立性低促性腺激素性性腺功能减退病例中已经鉴定出一些参与下丘脑 - 垂体 - 性腺成熟级联反应的基因,但许多调节青春期开始的基因仍未确定。对于青春期延迟和/或原发性闭经的情况,全面的临床检查,包括详细的既往史,将评估第二性征的发育情况,核实是否与生长迟缓有关,并寻找与病因诊断相关的特定指示性特征。如有必要,通过生物学、超声、放射学和遗传学检查完成这项临床检查,将试图确定哪些女孩会出现性腺、垂体或下丘脑起源的永久性性幼稚状态,哪些女孩会经历自发但延迟的青春期,以及哪些女孩有原发性闭经但第二性征已发育。治疗方案必须综合考虑病因、身高预后、骨质保存和心理因素。