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与睾丸横过异位相关的持续性苗勒管综合征的临床特征及分子遗传学:三例报告

Clinical aspects and molecular genetics of persistent müllerian duct syndrome associated with transverse testicular ectopia: report of three cases.

作者信息

Ju Xiaobing, Li ZhongXing, Zhang Chao, Qin Chao, Shao Pengfei, Li Jie, Li Pu, Cao Qiang, Zhang Wei, Wang Zengjun, Yin Changjun

机构信息

Department of Urology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China.

出版信息

Urol Int. 2013;90(1):83-6. doi: 10.1159/000339599. Epub 2012 Nov 9.

Abstract

Persistent müllerian duct syndrome (PMDS) is a rare form of male pseudohermaphroditism, characterized by the presence of a uterus and fallopian tubes owing to failure of müllerian duct regression in genotypically normal males. The association between a persistent müllerian duct and transverse testicular ectopia (TTE) is even more uncommon. PMDS with TTE is a very rare pathological association, often discovered during repair for inguinal hernia or cryptorchidism. We report 3 cases of Chinese patients with PMDS associated with TTE. Hysterectomy was performed, with resection of the underdeveloped fallopian tubes. Both gonads were placed into subdartos pouches in each scrotum by the transseptal approach. PMDS with TTE is a rarely encountered form of male pseudohermaphroditism usually unexpectedly found at surgery for cryptorchidism or inguinal hernia. Surgical treatment should avoid damage of fertile testes and vasa deferens.

摘要

持续性苗勒管综合征(PMDS)是一种罕见的男性假两性畸形,其特征是在基因型正常的男性中,由于苗勒管退化失败而出现子宫和输卵管。持续性苗勒管与睾丸横过异位(TTE)之间的关联更为罕见。伴有TTE的PMDS是一种非常罕见的病理关联,常在腹股沟疝修补术或隐睾症手术中发现。我们报告3例中国PMDS合并TTE患者。进行了子宫切除术,并切除了发育不全的输卵管。通过经中隔入路将双侧性腺置于每个阴囊的肉膜囊内。伴有TTE的PMDS是一种罕见的男性假两性畸形,通常在隐睾症或腹股沟疝手术中意外发现。手术治疗应避免损伤有生育能力的睾丸和输精管。

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