【新增男性内假两性畸形3例】。

Chirurgie pediatrique Pub Date : 1990-01-01
J P Giraud, J G Yao
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引用次数: 0

摘要

本文报告3例男性内假两性畸形新病例。它是一个稀缺的实体。在疝气或隐睾的治疗过程中,这一发现是艰难的。家族病史没有什么特别的。这种综合征的主要问题是治疗。我们的态度是保留苗勒管衍生物和治疗疝气或隐睾。子宫切除术不合理的原因如下:目前还没有关于苗勒管衍生物癌变的报道。输精管与子宫关系密切;因此,解剖是危险的。为了保护生育能力,我们没有进行系统的阉割。考虑到癌变的主要风险,只有当腺体在腹腔内且无法切除时,才进行睾丸切除。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[3 new cases of internal male pseudohermaphroditism].

The authors report 3 new cases of Male Internal Pseudohermaphrodism. It is a scarce entity. The discovery is fortuous during the cure of hernia or cryptorchidism. The family history has nothing particular. The main problem of this syndrome is its treatment. Our attitude consisted in conserving the mullerian derivatives and treating the hernia or the cryptorchidism. Hysterectomy is not justified for the following reasons; no case of cancerisation of the mullerian derivatives has not yet been reported. The vasa deferens and uterus are in intimate relationship; the dissection is therefore dangerous. We did not perform systematic castration in order to protect fertility. The removal of the testis is performed only when the gland is intraabdominal and undescendable considering the major risk of cancerisation.

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