首页> 外文期刊>Medical Case Studies >An unusual case of inguinal hernia: Persistent mullerian duct syndrome with transversetesticular ectopia
【24h】

An unusual case of inguinal hernia: Persistent mullerian duct syndrome with transversetesticular ectopia

机译:腹股沟疝的不寻常病例:持续性苗勒氏管综合征伴睾丸横突

获取原文
       

摘要

Persistent Müllerian Duct syndrome (PMDS) is a rare variety of male pseudo-hermaphroditism. It is characterized by the persistence of the uterus, fallopian tubes and upper vagina in otherwise normally virilized boys. The association of the syndrome called?transverse testicular ectopia (TTE), a condition in which both testes are located in one inguinal canal is rare. Here, we report a young male patient presented with infertility, left sided inguinal hernia and right-sided undescended testis since birth, finally found to have PMDS with TTE.
机译:持续性苗勒氏管综合征(PMDS)是一种罕见的男性假性雌雄同体性疾病。它的特征是,在正常情况下被男性化的男孩中,子宫,输卵管和上阴道持续存在。称为“睾丸横突性异位症”(TTE)的综合症很少见,这种情况是两个睾丸都位于一条腹股沟管内。在这里,我们报道了一名年轻男性患者,自出生以来就表现出不育,左侧腹股沟疝和右侧睾丸未降,最后发现他们患有PMDS和TTE。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号