Laparoscopic sacrocolpopexy in a patient with vault prolapse of the sigmoid stump after vaginoplasty in Mayer-Rokitansky-Küster-Hauser syndrome: A case report

Case Reports in Women's Health

Ratih Krisna¹  Tokumasa Hayashi²  Pattiya Nutthachote³  Auran Rosanne Cortes³  Shino Tokiwa³  Masayoshi Nomura³  Yogo Sawada³  Manisha Yadav³ 

[1] Urogynecology Center, Kameda Medical Center, Kamogawa, Chiba, Japan;Corresponding author at: Urogynecology Center, Kameda Medical Center, 929 Higashicho, Kamogawa, Chiba, Japan.;Urogynecology Center, Kameda Medical Center, Kamogawa, Chiba, Japan;

关键词: Mayer-Rokitansky-Küster-Hauser syndrome;    Sigmoid stump prolapse;    Laparoscopic sacrocolpopexy;    Neovagina;   

DOI  :  

来源: DOAJ

【 摘 要 】

Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome is a rare congenital anomaly that results in Müllerian agenesis that affects the uterus and upper two-thirds of the vagina. Sigmoid vaginoplasty is a surgical treatment option; however, vaginal prolapse may result as a complication of the sigmoid neovagina. There are no standards for treatment due to the rarity of this condition. We present the case of a 59-year-old woman with a history of sigmoid vaginoplasty who underwent laparoscopic sacrocolpopexy (LSC) for grade IV sigmoid stump prolapse. The patient had a successful outcome and no evidence of recurrent prolapse. This clinical case reveals the feasibility of LSC as a surgical treatment for sigmoid stump prolapses in patients with MRKH syndrome.

【 授权许可】

Unknown