[Inappropriate sexual differentiation of sex reversal type in 16-year-old boy with male phenotype].

Jerzy Starzyk, Aleksandra Górska, Dominika Januś
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Abstract

We present a case of a 16-year-old boy with gynecomastia and symptoms of delayed puberty (relatively small testes and penis), who attended the Endocrinology Clinic. Pubic hair development was normal. Basic hormonal blood tests showed a primary testicular lesion (hypergonadotropic hypogonadism). The result of karyotype examination showed female karyotype 46, XX. Based on those results the boy was diagnosed to be 46, XX male. A replacement testosterone therapy was administered. He stays in follow-up for gonad observation. The authors emphasize the possibility of establishing the diagnosis of a severe disorder belonging to the group of inappropriate sex differentiation of sex reversal type not earlier than in teenage adolescents, who present symptoms of delayed puberty. In such cases the main rule in establishing a final diagnosis is played by a physical examination with evaluation of sex development, as well as basic hormonal blood tests and karyotype result. Their correct interpretation is possible only by a physician who has reliable knowledge of the physiology of male sex determination.

[16岁男性表现型男孩性反转型的不适当性分化]。
我们报告一个16岁的男性男性乳房发育症和青春期延迟的症状(相对较小的睾丸和阴茎),谁参加了内分泌诊所。阴毛发育正常。基本的激素血液检查显示原发性睾丸病变(促性腺激素亢进性性腺功能减退)。核型检查结果为女性核型46,XX。根据这些结果,该男孩被诊断为46岁,XX岁男性。给予替代睾酮治疗。他继续进行性腺观察。作者强调,不早于出现青春期延迟症状的青少年,建立属于性逆转型不适当性别分化组的严重障碍的诊断的可能性。在这种情况下,确定最终诊断的主要规则是通过评估性发育的身体检查,以及基本的激素血液检查和核型结果。只有具备男性性别决定生理方面可靠知识的医生才有可能对其作出正确的解释。
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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