Department of Pediatric Endocrinology, Diabetes, and Metabolism, University of South Florida, All Children's Hospital, 501 Sixth Ave S, Box 6900, St Petersburg, FL 33701, USA.
Pediatrics. 2010 Sep;126(3):e728-33. doi: 10.1542/peds.2010-0596. Epub 2010 Aug 16.
Testotoxicosis, a form of gonadotropin-independent precocious puberty, results from an activating mutation of the luteinizing hormone receptor expressed in testicular Leydig cells. Affected males experience early testosterone secretion, virilization, advancing bone age, and resultant short stature. Recently, the use of combination therapy with a potent antiandrogen agent (bicalutamide) and a third-generation aromatase inhibitor (anastrozole or letrozole) was reported to yield encouraging short-term results. We present here the results of longer-term treatment (4.5 and 5 years) with this combination therapy in 2 boys who demonstrated that it is well tolerated, slows bone-age advancement in the face of continued linear growth, and prevents progression of virilization.
Testotoxicosis,一种促性腺激素依赖性性早熟的形式,是由于黄体生成素受体的激活突变引起的,该受体在睾丸间质细胞中表达。受影响的男性会出现早期的睾丸酮分泌、男性化、骨龄提前和由此导致的身材矮小。最近,报道了使用联合治疗方案,即使用一种有效的抗雄激素药物(比卡鲁胺)和第三代芳香酶抑制剂(阿那曲唑或来曲唑),取得了令人鼓舞的短期效果。我们在此介绍了该联合治疗方案在 2 名男孩中进行的更长时间(4.5 年和 5 年)治疗的结果,表明该方案耐受性良好,在持续线性生长的情况下减缓骨龄进展,并防止男性化进展。