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[伴有精原细胞瘤的持续性苗勒管综合征:一例报告]

[Persistent Müllerian duct syndrome with seminoma: report of a case].

作者信息

Morikawa M, Wakabayashi A, Nakata Y, Tokunaka S, Takamura T, Yachiku S

出版信息

Hinyokika Kiyo. 1985 Oct;31(10):1819-29.

PMID:4091131
Abstract

Persistent Müllerian duct syndrome is a male hermaphroditism in which remnants of Müllerian ducts occur from abnormality of Müllerian inhibitory factor and often cause transverse testicular ectopia or hernia uteri inguinalis. A 22-year-old-man was admitted with the chief complaint of painless swelling of the right scrotal content. Preoperative diagnosis was right testicular tumor and left undescended testis. High orchiectomy was done. At operation left transverse testicular ectopia and a remnant Müllerian duct was found incidentally. The right testicular tumor was seminoma pT1. Sixty-seven cases of transverse testicular ectopia have been reported in Japan, 37 of which are reports of a remnant Müllerian duct. Ten of these cases were accompanied by tumors. The pathogenesis and treatment of persistent Müllerian duct syndrome were discussed with review of the literature.

摘要

持续性苗勒管综合征是一种男性两性畸形,由于苗勒管抑制因子异常,导致苗勒管残余存在,常引起睾丸横过异位或子宫腹股沟疝。一名22岁男性因右侧阴囊内容物无痛性肿胀为主诉入院。术前诊断为右侧睾丸肿瘤和左侧隐睾。行高位睾丸切除术。术中偶然发现左侧睾丸横过异位及一条苗勒管残余。右侧睾丸肿瘤为pT1期精原细胞瘤。日本已报道67例睾丸横过异位病例,其中37例报告有苗勒管残余。这些病例中有10例伴有肿瘤。结合文献复习,对持续性苗勒管综合征的发病机制及治疗进行了讨论。

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