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伴有髓质海绵肾、无性腺症和持续睾酮分泌的贝克威思-维德曼综合征

Beckwitt-Wiedemann's syndrome with medullary sponge kidneys, agonadism and persistent testosterone production.

作者信息

Salgado A L, Macia A L, Freire A, Paramo P, Fernandez-Cruz A

出版信息

Eur Urol. 1977;3(2):108-10. doi: 10.1159/000472070.

Abstract

A patient with Beckwitt-Wiedemann's syndrome is described in which associated malformations were hemihypertrophy of the body, medullary sponge kidneys and absence of testes and internal ducts. On the other hand, we demonstrated biochemically the existence of testosterone secretion, with active response to a 3-day HCG stimulation as well as prepuberty levels LH and FSH. This demonstrated the existence of functioning Leydig's cells. The diagnosis of agonadism and anorchia could not be entirely true since they lead to an erroneous conclusion that there always are some disseminated Leydig's cells.

摘要

本文描述了一名患有贝克威思-维德曼综合征的患者,其相关畸形包括身体半侧肥大、髓质海绵肾以及睾丸和内生殖器缺如。另一方面,我们通过生化检测证实了睾酮分泌的存在,对3天的人绒毛膜促性腺激素刺激有活跃反应,同时促黄体生成素和促卵泡生成素水平处于青春期前水平。这证明了存在功能正常的睾丸间质细胞。性腺发育不全和无睾症的诊断并不完全准确,因为它们会导致一个错误的结论,即总是存在一些散在的睾丸间质细胞。

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