首页> 外文期刊>BMC Urology >A modified neo-vagina procedure in a low resource urogynecological unit: a case report of a 21?year old with Mayer-Rokitansky-Küster-Hauser (mrkh) Syndrome operated at Mbarara referral hospital, Southwestern Uganda
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A modified neo-vagina procedure in a low resource urogynecological unit: a case report of a 21?year old with Mayer-Rokitansky-Küster-Hauser (mrkh) Syndrome operated at Mbarara referral hospital, Southwestern Uganda

机译:在低资源辅音学单位的改进的新阴道程序:一个21岁的案例报告与Mayer-Rokitansky-Küster-hauser(MRKH)综合征在乌干达西南部Mbarara推荐医院运营

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Background Although vaginal agenesis as may occur in Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome is a rare condition, it is associated with not only anatomical problems but also serious psychological and social problems like painful sexual intercourse, primary amenorrhea and infertility. Surgery, which is aimed at reconstruction of a vagina of adequate length and width to serve the function, is the main method of treatment. Many methods for vaginal reconstruction have been described but each has its complications and limitations. The most commonly preferred procedure for treating this condition is the McIndoe vaginoplasty which involves dissection into the recto-vesical space, inserting two split thickness skin grafts folded over a mold in this newly created space and regular dilatation of the neovagina postoperatively to avoid stenosis. However surgeons with this expertise in this part of the world are rare to find and where they are available, the special molds on which to fold the skin grafts into the neovaginal space are not readily available. Case presentation A 21-year-old female with vaginal agenesis was operated on using a modification of the McIndoe procedure using a cylinder of a 60cm3 syringe as a vaginal mold/form and kept in place. We left a Foley in place for 10?days and we did a dye test after removing the syringe to ensure that there was no leakage resulting from fistula formation. Conclusion The operation was successful and on subsequent monthly reviews of the patient, she has a patent functional vagina of about 9?cm in length at 8?months after the operation with resumption of sexual intercourse.
机译:背景技术虽然阴道验血如可能发生在Mayer-Rokitansky-küster-hauser(MRKH)综合征中是一种罕见的条件,但它不仅与解剖问题有关,而且与痛苦的性交,原发性闭经和不孕症等严重的心理和社会问题有关。手术,旨在重建足够长和宽度的阴道,以满足该功能,是主要的治疗方法。已经描述了许多用于阴道重建的方法,但每个都有其并发症和限制。治疗这种条件的最常见优选的程序是McIndoe阴道成形术,涉及解剖到直接弱空间,在新创造的空间中插入两种分裂厚度皮肤移植物,并在术后术后常规地扩张Neovagina以避免狭窄。然而,在世界这一部分的这种专业知识的外科医生很难找到,并且在哪里可以在哪里折叠皮肤移植进入Neovaginal空间的特殊模具。案例介绍使用使用60cm 3 / sup>注射器的气缸作为阴道模具/形式的圆柱体的Mcindoe程序进行了一个21岁的阴道血液发生的女性,并将其保持在适当位置。我们留下了一个Foley 10?天,我们在去除注射器后做了一种染料测试,以确保没有由瘘管形成产生的泄漏。结论该行动成功,并在随后的患者的每月审查时,她在恢复性交后8月8日在8次上长约9厘米的专利职能阴道。

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