A Rare Case of OHVIRA Syndrome with Urethral Stenosis

Ketul R Patel, N. Sadasukhi, T. Sadasukhi, M. Gupta, H. Gupta, Ashish Sharma, Sandeep Malik
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Abstract

A bstrAct Obstructed hemivagina and ipsilateral renal anomaly (OHVIRA) is a rare anomaly of the urogenital system. The characteristic triad of this syndrome, which was initially reported in 1950, is didelphys uterus, obstructed hemivagina, and ipsilateral renal agenesis (Embrey 1 ). The prevalence of congenital Müllerian duct anomalies is reported to be 1%. 2 A 24-year-old girl got admission to MGH on 15.3.2019 with lower abdominal pain and difficulty in the passing of urine. Her menarche was established 6 months back with a regular cycle and associated with dysmenorrhea. Magnetic resonance imaging (MRI) established the diagnosis of OHVIRA. She underwent surgery for drainage of the hematocolpos and excision of the vaginal septum and urethral dilatation with cystoscopy followed by an uncomplicated recovery and the patient had normal menstrual cycles after surgery.
OHVIRA综合征合并尿道狭窄1例
梗阻性半阴道伴同侧肾异常(OHVIRA)是一种罕见的泌尿生殖系统异常。该综合征的特征性三联征最初于1950年报道,为子宫双陷、半阴道梗阻和同侧肾发育不全(Embrey 1)。据报道,先天性勒管异常的发生率为1%。2一名24岁女孩于2019年3月15日因下腹疼痛、排尿困难入院。6个月前开始月经初潮,月经周期正常,伴有痛经。磁共振成像(MRI)确立了OHVIRA的诊断。她接受了直肠引流术、阴道间隔切除术和膀胱镜下尿道扩张术,术后恢复顺利,月经周期正常。
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