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46,XY性腺发育不全中的睾丸分化异常:形态学、内分泌学、血清学

Aberrant testicular differentiation in 46,XY gonadal dysgenesis: morphology, endocrinology, serology.

作者信息

Wolman S R, McMorrow L E, Roy S, Koo G C, Wachtel S S, David R

出版信息

Hum Genet. 1980;55(3):321-5. doi: 10.1007/BF00290211.

Abstract

In an infant with gonadal dysgenesis and somatic anomalies, the internal and external genitalia were female but the gonads contained tubular structures suggesting male differentiation. The karyotype was 46,XY with no evidence of structural aberration or mosaicism. Hormonal metabolism and H-Y antigen expression were assayed in cultured gonadal cells. Although unable to synthesize testosterone, the cultured cells were able to convert it to dihydrotestosterone. H-Y antigen was present, perhaps at a level lower than that in cells from normal XY males. Our observations indicate that a modicum of testicular organogenesis may precede the involution that results in a streak gonad in some cases of gonadal dysgenesis.

摘要

在一名患有性腺发育不全和躯体异常的婴儿中,其内外生殖器为女性,但性腺包含管状结构,提示存在男性分化。核型为46,XY,无结构畸变或嵌合体证据。对培养的性腺细胞进行了激素代谢和H-Y抗原表达检测。尽管培养的细胞无法合成睾酮,但能够将其转化为双氢睾酮。存在H-Y抗原,其水平可能低于正常XY男性细胞中的水平。我们的观察结果表明,在某些性腺发育不全病例中,少量的睾丸器官发生可能先于导致条索状性腺的退化过程。

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