Laue L, Comite F, Hench K, Loriaux D L, Cutler G B, Pescovitz O H
Am J Dis Child. 1985 Nov;139(11):1097-100. doi: 10.1001/archpedi.1985.02140130035025.
Seven children with central precocious puberty and either neurofibromatosis and/or optic gliomas were referred to the National Institutes of Health, Bethesda, Md, for evaluation and treatment with the long-acting luteinizing hormone releasing hormone analogue (LHRHa) D-Trp6-Pro9-NEt-LHRH. Only six of the seven children chose to receive treatment. Four children presented with neurofibromatosis, three of whom also had optic gliomas; the remaining three children had isolated optic gliomas, without other neurocutaneous stigmas. All had central precocious puberty mediated by activation of the hypothalamic-pituitary-gonadal axis. Six months of LHRHa therapy caused suppression of gonadotropin and sex steroid levels, stabilization or regression of secondary sexual characteristics, and decreases in growth velocity and the rate of bone age maturation. We conclude that LHRHa therapy is effective in the treatment of central precocious puberty secondary to neurofibromatosis and/or optic gliomas.
七名患有中枢性性早熟且伴有神经纤维瘤病和/或视神经胶质瘤的儿童被转诊至马里兰州贝塞斯达的国立卫生研究院,以接受长效促黄体生成素释放激素类似物(LHRHa)D-Trp6-Pro9-NEt-LHRH的评估和治疗。七名儿童中只有六名选择接受治疗。四名儿童患有神经纤维瘤病,其中三名还患有视神经胶质瘤;其余三名儿童患有孤立性视神经胶质瘤,无其他神经皮肤体征。所有患儿均因下丘脑-垂体-性腺轴激活而导致中枢性性早熟。六个月的LHRHa治疗导致促性腺激素和性类固醇水平受到抑制,第二性征稳定或消退,生长速度和骨龄成熟率降低。我们得出结论,LHRHa治疗对神经纤维瘤病和/或视神经胶质瘤继发的中枢性性早熟有效。