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先天性阴道缺失合并宫颈发育不全患者的生殖道重建术。

Genital tract reconstruction in a patient with congenital absence of the vagina and hypoplasia of the cervix.

作者信息

Cukier J, Batzofin J H, Conner J S, Franklin R R

出版信息

Obstet Gynecol. 1986 Sep;68(3 Suppl):32S-36S.

PMID:3526221
Abstract

A 15-year-old female presented with congenital absence of the vagina and a blind ending hypoplastic cervix. The uterine cavity appeared normal by ultrasound examination, and the patient experienced molimina. Cognizant of risks and failures of described attempts at correction, reconstruction was performed using a series of stents covered with skin grafts. At 21 months postoperatively, the patient now has a functioning vagina and menstruates regularly. The desire to avoid a hysterectomy coupled with new alternatives in the management of the infertile patient resulted in the approach described.

摘要

一名15岁女性因先天性阴道缺如和宫颈发育不全呈盲端就诊。超声检查显示子宫腔正常,患者有经前期症状。考虑到已描述的矫正尝试存在风险和失败情况,采用了一系列覆盖皮肤移植片的支架进行重建。术后21个月,患者现拥有功能正常的阴道且月经规律。避免子宫切除术的意愿以及不育患者管理方面的新选择促成了所述治疗方法的采用。

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Genital tract reconstruction in a patient with congenital absence of the vagina and hypoplasia of the cervix.先天性阴道缺失合并宫颈发育不全患者的生殖道重建术。
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