Leiper A D, Stanhope R, Preece M A, Grant D B, Chessells J M
Department of Haematology, University of London, UK.
Horm Res. 1988;30(2-3):72-6. doi: 10.1159/000181032.
We have studied 41 children with early or precocious puberty who have been treated for acute lymphoblastic leukaemia with prophylactic cranial irradiation (1,800-2,400 cGy) accompanied by intrathecal methotrexate and systemic chemotherapy. Mean age at radiotherapy was 3.9 years (range 1.7-7.7) in the girls and 4.8 years (range 2.6-7.8) in the boys. Mean age at the onset of puberty was 8.6 years (range 6.7-9.7) in the girls and 9.3 years (range 7.8-10.3) in the boys. Of the 41 children with early puberty (greater than 1.4 SD from the mean) 36 were females and 5 were males. 21 of the 36 girls had an absent or inadequate growth acceleration of puberty. 7 of 12 girls who had a pharmacological test of growth hormone (GH) secretion had GH insufficiency (peak level less than 20 mU/l). Early or precocious puberty combined with GH insufficiency may produce severe growth failure and we have used a treatment regimen of a gonadotrophin-releasing hormone analogue, in order to reduce the rate of epiphyseal maturation, combined with biosynthetic GH to increase or sustain growth rate. We have treated 4 girls in this manner. During a mean treatment period of 0.86 years, height SDS for bone age rose from a mean of -1.06 to -0.59. Longer treatment periods will be required to assess the effect on final height.
我们研究了41例患有性早熟的儿童,这些儿童曾接受预防性颅脑照射(1800 - 2400 cGy)联合鞘内注射甲氨蝶呤及全身化疗以治疗急性淋巴细胞白血病。放疗时女孩的平均年龄为3.9岁(范围1.7 - 7.7岁),男孩为4.8岁(范围2.6 - 7.8岁)。女孩青春期开始的平均年龄为8.6岁(范围6.7 - 9.7岁),男孩为9.3岁(范围7.8 - 10.3岁)。在这41例性早熟儿童(高于均值1.4个标准差)中, 36例为女性,5例为男性。36例女孩中有21例青春期生长加速缺失或不足。在12例接受生长激素(GH)分泌药物试验的女孩中,7例存在GH不足(峰值水平低于20 mU/l)。性早熟合并GH不足可能导致严重的生长发育迟缓,我们采用了促性腺激素释放激素类似物治疗方案,以降低骨骺成熟速率,并联合使用生物合成GH来提高或维持生长速率。我们用这种方法治疗了4例女孩。在平均0.86年的治疗期间,骨龄的身高标准差评分从平均 -1.06升至 -0.59。需要更长的治疗时间来评估对最终身高的影响。