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持续性苗勒管结构导致的男性假两性畸形。

Male pseudohermaphroditism by persistent müllerian structures.

作者信息

Vazquez-Echarri J, De Yebenes A B

出版信息

Urology. 1984 Nov;24(5):446-51. doi: 10.1016/0090-4295(84)90319-4.

Abstract

We have studied 2 cases of nonfamilial male pseudohermaphroditism by persistent müllerian ducts. The first case, found in a fourteen-year-old male, can be described as the classic form of cryptorchism which resisted hormonal treatment and in which a rudimentary uterus with fallopian tubes and atrophic testicles were found at exploratory laparotomy. The second case was discovered in a thirty-nine-year-old man who had bilateral cryptorchism. He presented with an abdominal mass which was found to be a seminoma in the right intra-abdominal testicle, and a well-defined uterus with fallopian tubes and an atrophic left testicle were seen. Neither case presented phenotype disturbances. Both karyotypes were 46 XY. A total resection of the female sexual organs and testicles was performed in both patients, and the mass was removed in the second case. The tumoral degeneration of the intra-abdominal testicles in this syndrome is found in similar proportion to the simple cryptorchid testicles. Our second case is the tenth one of a testicular tumor in pseudohermaphroditism by persistent müllerian ducts to be reported in the literature.

摘要

我们研究了2例因苗勒管持续存在导致的非家族性男性假两性畸形病例。第一例患者为一名14岁男性,表现为典型的隐睾症,对激素治疗无效,在探查性剖腹手术中发现了一个带有输卵管的发育不全子宫和萎缩的睾丸。第二例患者是一名39岁男性,患有双侧隐睾症。他出现腹部肿块,经检查发现右侧腹内睾丸为精原细胞瘤,同时可见一个界限清晰的带有输卵管的子宫和萎缩的左侧睾丸。两例患者均未出现表型异常。二者的核型均为46 XY。两名患者均接受了女性性器官和睾丸的全切手术,第二例患者的肿块也被切除。该综合征中腹内睾丸的肿瘤变性发生率与单纯隐睾症相似。我们的第二例病例是文献报道的第10例因苗勒管持续存在导致的男性假两性畸形合并睾丸肿瘤的病例。

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