Tosti A, Iorizzo M, Piraccini B M
Department of Dermatology, University of Bologna, Via Massarenti 1, 40138 Bologna, Italy.
Br J Dermatol. 2005 Mar;152(3):556-9. doi: 10.1111/j.1365-2133.2004.06279.x.
Androgenetic alopecia (AGA) is the most common type of hair loss in adults. Although there are differences in the age at onset, the disease starts after puberty when enough testosterone is available to be transformed into dihydrotestosterone. We report 20 prepubertal children with AGA, 12 girls and eight boys, age range 6-10 years, observed over the last 4 years. All had normal physical development. Clinical examination showed hair loss with thinning and widening of the central parting of the scalp, both in boys and girls. In eight cases frontal accentuation and breach of frontal hairline were also present. The clinical diagnosis was confirmed by pull test, trichogram and dermoscopy in all cases, and by scalp biopsy performed in six cases. There was a strong family history of AGA in all patients. The onset of AGA is not expected to be seen in prepubertal patients without abnormal androgen levels. A common feature observed in our series of children with AGA was a strong genetic predisposition to the disease. Although the pathogenesis remains speculative, endocrine evaluation and a strict follow-up are strongly recommended.
雄激素性脱发(AGA)是成年人最常见的脱发类型。尽管发病年龄存在差异,但该疾病在青春期后开始,此时有足够的睾酮可转化为二氢睾酮。我们报告了过去4年中观察到的20例青春期前AGA患儿,其中12名女孩和8名男孩,年龄在6至10岁之间。所有患儿身体发育均正常。临床检查显示,男孩和女孩均有脱发,伴有头皮中央分缝处变细和变宽。8例还存在额部加重和额发际线破坏。所有病例均通过拔毛试验、毛发镜检和皮肤镜检查确诊,6例进行了头皮活检。所有患者均有强烈的AGA家族史。在青春期前且雄激素水平无异常的患者中,预计不会出现AGA发病。在我们的AGA患儿系列中观察到的一个共同特征是对该疾病有很强的遗传易感性。尽管发病机制仍属推测,但强烈建议进行内分泌评估和严格随访。