先天性肾上腺增生伴47,xxy Klinefelter综合征。

T Yamaguchi, H Abe, T Kuwano, T Sugimoto, K Chihara
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引用次数: 9

摘要

我们在这里描述一个独特的先天性肾上腺增生(CAH)伴有克兰费尔特综合征。一名日本男孩在出生时被诊断为21-羟化酶缺乏引起的CAH,但此后一直未得到治疗,直到10岁。与此同时,他在9岁时表现出明显的身体发育加速和性早熟,此时发育完全停止。在我们诊所的定期随访和10岁后的类固醇治疗中,他被认为是双侧睾丸小而坚硬。染色体检查和睾丸活检显示47xxy Klinefelter综合征合并CAH。这两种疾病的关联至今尚未见报道,本病例为我们所知的首例。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Congenital adrenal hyperplasia with 47, XXY Klinefelter syndrome.

We describe here a unique case of congenital adrenal hyperplasia (CAH) accompanied by Klinefelter syndrome. A Japanese boy was diagnosed as having CAH caused by 21-hydroxylase deficiency at birth, but was untreated thereafter until age 10. In the meantime he showed marked acceleration in somatic growth with sexual precocity by age 9, at which time growth completely stopped. During regular follow-ups at our clinic and steroid treatment after age 10, he was recognized as having bilateral small and firm testes. A chromosomal examination and a testicular biopsy revealed a complication of 47, XXY Klinefelter syndrome with CAH. Association of these two diseases has not been reported so far, and the present case is the first one to our knowledge.

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