[既往接受醋酸环丙孕酮治疗后,长期应用促性腺素类似物D-Trp-6-LHRH治疗女孩中枢性性早熟]。

Q4 Medicine Cesko-Slovenska Pediatrie Pub Date : 1994-01-01
M Snajderová, D Zemková, J Lebl, M Pechová, M Zounarová, S Kolousková
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引用次数: 0

摘要

一组5名患有中枢性性早熟(CPP)的女孩(4名患有特发性CPP的女孩和1名患有器质性CPP的女孩)接受平均17个月(12-20个月)的促性腺激素(aGnRH) D-Trp-6-LHRH(Triptorelin)激动剂,每4周通过i.m.途径治疗60-100微克/公斤。女孩在aGnRH治疗开始时的日历年龄(CA)为7.3 +/- 0.7岁,骨年龄(BA)为9.6 +/- 1.0岁。先前给予醋酸环丙孕酮的平均疗程为26个月(4-56个月),在12周内逐渐停用。aGnRH处理12个月后,生长速度从8.1 #/- 2.1 cm/年降至6.2 +/- 1.7 cm/年(NS)。治疗第一年结束时,骨龄增量从1.7 +/- 0.8下降到0.94 +/- 0.4 (NS)。预测成人身高在一年内没有变化(aGnRH治疗前158.6 +/- 5.3 cm,治疗一年后159.0 +/- 5.3 cm)。在所有女孩中,在最初的醋酸环丙孕酮治疗期间,早熟已经被阻止。在aGnRH治疗期间,除1例患者外,未记录进展。在这名患有特发性CPP的女孩中,作者观察到从第四个月开始,在常规给药雷普雷林期间,终止迄今为止给予的醋酸环丙孕酮治疗后的二次治疗失败的临床和生化表现-“逃避治疗”。加用醋酸环丙孕酮后,临床及激素指标均有改善。这个病人没有麦克恩-奥尔布赖特综合症的典型症状。
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[Long-term therapy of central precocious puberty in girls with the gonadoliberin analog D-Trp-6-LHRH after prior therapy with cyproterone acetate].

A group of five girls with central precocious puberty (CPP) (four girls with idiopathic CPP and one girl with organically conditioned CPP) were treated for a mean period of 17 months (12-20 months) with an agonist of gonadoliberine (aGnRH) D-Trp-6-LHRH(Triptorelin), 60-100 micrograms/kg by the i.m. route, every four weeks. The calendar age (CA) of the girls was at the onset of aGnRH treatment 7.3 +/- 0.7 years, the bone age (BA) 9.6 +/- 1.0 years. Previously Cyproterone acetate treatment administered for an average period of 26 months (4-56 months) was gradually discontinued in the course of 12 weeks. After 12 months aGnRH treatment the growth rate slowed down from 8.1 #/- 2.1 to 6.2 +/- 1.7 cm/year (NS). The bone age increment per calendar year declined at the end of the first year of treatment from 1.7 +/- 0.8 to 0.94 +/- 0.4 (NS). Prediction of the adult height did not change in the course of one year (before aGnRH therapy 158.6 +/- 5.3 after one year's treatment 159.0 +/- 5.3 cm). In all girls premature maturing was arrested already during the original Cyproterone acetate treatment. With the exception of a single patient during aGnRH therapy progression was not recorded. In this girl with the idiopathic form of CPP the authors observed during regular Triptorelin administration, starting from the fourth month, clinical and biochemical manifestations of secondary therapeutic failure after termination of hitherto administered Cyproterone acetate treatment-"escape from treatment". Clinical and hormonal indicators improved after addition of Cyproterone acetate. This patient lacks typical symptoms suggesting McCune-Albright's syndrome.

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来源期刊
Cesko-Slovenska Pediatrie
Cesko-Slovenska Pediatrie Medicine-Pediatrics, Perinatology and Child Health
CiteScore
0.30
自引率
0.00%
发文量
32
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