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台湾女孩同性性早熟的病因及临床特征:台湾大学医院23年的经验

Etiology and clinical features of isosexual precocious puberty in Taiwanese girls: twenty-three years' experience in National Taiwan University Hospital.

作者信息

Lee Cheng-Ting, Tung Yi-Ching, Tsai Wen-Yu

机构信息

Department of Pediatrics, National Taiwan University Hospital and College of Medicine, National Taiwan University, Taipei, Taiwan.

出版信息

J Pediatr Endocrinol Metab. 2009 Oct;22(10):947-53. doi: 10.1515/jpem.2009.22.10.947.

DOI:10.1515/jpem.2009.22.10.947
PMID:20020583
Abstract

The aim of this study was to elucidate the etiology and clinical features of Taiwanese girls with isosexual precocious puberty. 460 girls with precocious puberty were enrolled in this study. 284 of them had a GnRH test and 179 girls with gonadotropin-dependent precocious puberty (GDPP) underwent brain MRI. Our results showed 7% of these 460 girls had gonadotropin-independent precocious puberty (GIPP). The other 93% patients had GDPP and 96% of them were idiopathic. Functional ovarian cyst and hypothalamic hamartoma were leading causes of GIPP and organic GDPP, respectively. The presence of undetectable basal serum FSH and LH levels had a specificity of 95% in girls with GIPP. Among girls with GDPP, those aged < 5 years had a higher percentage of detected CNS lesions than older girls (8% vs 3%). Girls with organic CNS lesions also had more advanced bone age SDS (6.9 +/- 3.3 vs 3.3 +/- 1.9), larger uterine volume (13.8 +/- 12.1 vs 6.6 +/- 8.1 cm3), higher basal serum estradiol (33.5 +/- 17.1 vs 26.8 +/- 18.2 pg/ml), and higher peak LH level after GnRH stimulation (45.2 +/- 36.2 vs 25.8 +/- 27.3 U/l) than those with idiopathic GDPP. In conclusion, GIPP is uncommon in Taiwanese girls with precocious puberty. Functional ovarian cyst and hypothalamic hamartoma are leading causes of GIPP and organic GDPP, respectively. The presence of neurological deficit, younger age at onset of puberty, presence of menstruation, rapid advance of bone age, markedly enlarged uterus, high serum estradiol, and high peak LH level after GnRH stimulation are suggestive of organic GDPP.

摘要

本研究的目的是阐明台湾地区同性性早熟女童的病因及临床特征。本研究纳入了460例性早熟女童。其中284例进行了GnRH试验,179例促性腺激素依赖性性早熟(GDPP)女童接受了脑部MRI检查。我们的结果显示,这460例女童中有7%患有非促性腺激素依赖性性早熟(GIPP)。其他93%的患者患有GDPP,其中96%为特发性。功能性卵巢囊肿和下丘脑错构瘤分别是GIPP和器质性GDPP的主要病因。在GIPP女童中,基础血清FSH和LH水平检测不到的特异性为95%。在GDPP女童中,年龄<5岁的女童中枢神经系统病变检出率高于年龄较大的女童(8%对3%)。与特发性GDPP女童相比,患有器质性中枢神经系统病变的女童骨龄标准差也更高(6.9±3.3对3.3±1.9)、子宫体积更大(13.8±12.1对6.6±8.1 cm³)、基础血清雌二醇水平更高(33.5±17.1对26.8±18.2 pg/ml)以及GnRH刺激后LH峰值水平更高(45.2±36.2对25.8±27.3 U/L)。总之,GIPP在台湾地区性早熟女童中并不常见。功能性卵巢囊肿和下丘脑错构瘤分别是GIPP和器质性GDPP的主要病因。存在神经功能缺损、青春期发病年龄较小、出现月经、骨龄快速进展、子宫明显增大、血清雌二醇水平高以及GnRH刺激后LH峰值水平高提示为器质性GDPP。

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Etiology and clinical features of isosexual precocious puberty in Taiwanese girls: twenty-three years' experience in National Taiwan University Hospital.台湾女孩同性性早熟的病因及临床特征:台湾大学医院23年的经验
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引用本文的文献

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Etiology of precocious puberty, 10 years study in Endocrine Reserch Centre (Firouzgar), Tehran.性早熟的病因学,在德黑兰内分泌研究中心(菲鲁兹加尔)进行的10年研究。
Iran J Reprod Med. 2012 Jan;10(1):1-6.
2
Sclerosing stromal tumour of the ovary presenting as precocious puberty: a rare neoplasm.表现为性早熟的卵巢硬化性间质瘤:一种罕见的肿瘤。
BMJ Case Rep. 2014 Mar 31;2014:bcr2013201124. doi: 10.1136/bcr-2013-201124.
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Juvenile granulosa cell tumor presenting as isosexual precocious puberty: A case report and review of literature.以同性性早熟为表现的青少年颗粒细胞瘤:一例报告并文献复习
Indian J Endocrinol Metab. 2013 Jan;17(1):157-9. doi: 10.4103/2230-8210.107870.