[6岁9个月女童mcune - albright综合征致性早熟]。

Endokrynologia, diabetologia i choroby przemiany materii wieku rozwojowego : organ Polskiego Towarzystwa Endokrynologow Dzieciecych Pub Date : 2006-01-01

Beata Wikiera, Józef Wawro, Anna Noczyńska

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引用次数: 0

摘要

McCune-Albright综合征的特征是多骨纤维发育不良，“咖啡-au-lait”斑点和各种内分泌器官的自主功能亢进。作者提出的情况下，女孩在6岁9个月与性早熟(初潮III期)。高雌二醇水平(204 pg/ml)和低促性腺激素浓度以及给药后促性腺激素水平提示卵巢自主。盆腔超声检查发现卵巢囊肿。排除其他内分泌异常。在病人的皮肤上发现了一个单一的“咖啡精”斑点。显像、x线摄影和计算机断层扫描显示右胫骨、上颌窦和蝶窦纤维性骨发育不良。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

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[Precocious puberty caused by McCune-Albright syndrome in a girl aged 6 years and 9 months].

The McCune-Albright syndrome is characterised by polyostotic fibrous dysplasia, "cafe-au-lait" spots and autonomous hyperfunction of various endocrine organs. The authors present the case of a girl at the age of 6 years 9 months with precocious puberty (thelarche III, menarche). High estradiol level (204 pg/ml) and low gonadoptopins concentration as well as their level after GnRH administration suggested ovarian autonomy. Ovarian cysts were found on pelvic ultrasound. Other endocrine abnormalities were excluded. Single "cafe-au-lait" spot was found on the patient skin. Scintigraphy, radiography and computed tomography scans showed fibrous dysplastic bones in the right tibia and in maxillary and sphenoid sinuses.

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Endokrynologia, diabetologia i choroby przemiany materii wieku rozwojowego : organ Polskiego Towarzystwa Endokrynologow Dzieciecych

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