Sigmoid vajinoplasti: olgu sunumu
Abstract
Özet
Mayer-Rokitansky-Küster-Hauser (MRKH) sendromu, uterovajinal ageneziye bağlı primer amenorenin nadir bir konjenital nedenidir. Yeniden vajen oluşturulmasında kulanılan çeşitli cerrahi teknikler vardır. Sigmoid greft uygulaması, yeterli uzunluğun sağlanabilmesi, doğal lubrikasyon ve erken cinsel fonksiyon kazanımı açısından en iyi yöntem olarak görülmektedir. Yirmi sekiz yaşında primer amenore ve ilk evliliğinde başarısız koitus öyküsü bulunan hastamız, vajinoplasti isteği ile kliniğimize başvurdu. Olguya sigmoid vajinoplasti operasyonu yapıldı. Postoperatif altıncı ayda evlilik yaptı ve 1.5 yıllık takipte herhangi bir komplikasyon görülmedi.
Anahtar sözcükler: Mayer-Rokitansky-Küstner-Hauser sendromu, sigmoid vajinoplasti
Abstract
The Mayer-Rokitansky-Küstner-Hauser (MRKH) syndrome is a rare congenital cause of primary amenorrhea, due to uterovaginal agenesis. Several surgical techniques have been used to create a neovagina. Neovagina construction with a sigmoid graft appears to be the best option, as it offers adequate length and natural lubrication, allowing early intercourse. A 28 years old women presented to our clinic with primary amenore and unsuccessful coitus at her first marriage whishing vaginoplasty. Sigmoid vaginoplasty performed for the patient. Six months after the operation our case had a marriage. For the one and a half year follow up no complication observed.
Keywords: Mayer-Rokitansky-Kustner-Hauser syndrome, sigmoid vaginoplastyKeywords
References
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Details
Primary Language
turc
Subjects
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Journal Section
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Publication Date
March 11, 2010
Submission Date
June 8, 2009
Acceptance Date
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Published in Issue
Year 2010 Volume: 32 Number: 1