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Uterus Didelphys with Obstructed Right Hemivagina, Ipsilateral Renal Agenesis and Right Pyocolpos: A Case Report

机译:子宫右冠状动脉梗阻,同侧肾发育不全和右脓疱的双峰症:一例报告

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摘要

Uterus didelphys with obstructed hemivagina and ipsilateral renal agenesis (OHVIRA Syndrome) is a rare congenital anomaly of the female genital tract. Uterus didelphys occurs when the midline fusion of the mullerian ducts is arrested, either completely or incompletely. Women with didelphic uterus may be asymptomatic and unaware of having a double uterus. They may present with complaints of dysmenorrhoea and dyspareunia. A 25 year old woman attending the infertility clinic at Nizwa regional referral hospital presented with history of dysmenorrhoea and foul vaginal discharge with right cystic pelvic mass. She was diagnosed as a case of double uterus with obstructed right hemivagina and right pyocolpos with ipsilateral renal agenesis after routine ultrasonography in the clinic followed by MRI. Excision of the right vaginal septum with drainage of 200 ml of purulent discharge was performed. She was relieved of her symptoms and conceived promptly after the surgical excision of the partial vaginal septum.
机译:子宫梗阻性偏瘫和同侧肾发育不全(OHVIRA综合征)是一种罕见的女性生殖道先天性异常。当缪勒氏管的中线融合完全或不完全被阻滞时,子宫就会发生子宫异位症。子宫双子宫的妇女可能没有症状,也没有意识到双子宫。他们可能会出现痛经和性交困难的主诉。一名25岁的妇女在尼兹瓦地区转诊医院的不孕症诊所就诊,有痛经史和白带积液,伴右囊性盆腔积液。在临床中常规超声检查后,经MRI检查,她被诊断为双子宫梗阻的右半窦和右pyocolpos伴同侧肾不发育。切除右阴道中隔,引流200 ml化脓性分泌物。手术切除部分阴道隔后,她的症状得到了缓解,并迅速怀孕。

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