Cloacal exstrophy variant in a female: A case report

Shelley Warner , Luciana Lerendegui , Monica D. Chow , David Lasko , Miguel Castellan , Felipe Pedroso
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Abstract

Introduction

Cloacal exstrophy is a rare birth defect that affects both the genitourinary and gastrointestinal tract, with an estimated incidence between 1:200,000 and 1:400,000 live births. The exact mechanism that leads to this defect is still unknown. Our purpose is to report a case of omphalocele-exstrophy-imperforate anus-spinal defect (OEIS) complex with a rare variant to add to the literature.

Case presentation

A 28-year-old female with no known medical history had a monochorionic diamniotic twin pregnancy. At 20 weeks of gestation a prenatal ultrasound demonstrated multiple fetal anomalies on twin B, including omphalocele, absent right kidney, non-visualization of bladder, and single umbilical artery. She had a scheduled Cesarean section at 34 weeks and 5 days of gestation. Twin B had a large omphalocele with an intact sac. Below the omphalocele, there was a cecal plate with a prolapsed ileum and a second small orifice corresponding to the hindgut. Two hemivaginas and hemiclitorises were appreciated inferior to the cecal plate but superior to a bladder plate bridge joining both halves. Each of the hemivaginas was connected to a hemiuterus with its own fallopian tube and ovary. The bladder was on both sides of the cecal plate and connected in the midline adopting a crescent shape with the concave side facing cephalad. Genetic testing confirmed an XX karyotype. On day-of-life 5 the patient underwent omphalocele repair and closure of the abdominal wall, tubularization of the cecal plate, and an end colostomy. Additionally, the hemivaginas and hemiclitorises were relocated to an orthotopic position and the bladder plates were joined together and used to cover part of the abdominal wall defect. She was discharged on day of life 42 with a weight of 2.72 kg. She continues to follow up outpatient. Her second stage procedure is still pending.

Conclusion

The position of the genital tract superior to the bladder exstrophy observed in this case has not been described before and is not fully explained by the current theories on the development of OEIS.

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一名女性的泄殖腔萎缩变异体:病例报告
导言泄殖腔萎缩是一种罕见的先天性缺陷,同时影响泌尿生殖道和胃肠道,估计发病率在1:200,000到1:400,000活产婴儿之间。导致这种缺陷的确切机制尚不清楚。我们的目的是报告一例脐膨出-肛门穿孔-脊柱缺损(OEIS)并伴有罕见变异的复杂病例,以补充相关文献。病例介绍 一名 28 岁女性,无已知病史,单绒毛膜双羊膜妊娠。妊娠 20 周时,产前超声检查显示双胎 B 胎儿多处畸形,包括卵脐带畸形、右肾缺失、膀胱未显影和单脐动脉。她在妊娠 34 周零 5 天时按计划进行了剖宫产手术。双胎 B 有一个大的脐膨出,脐囊完好无损。在脐带下方有一块盲肠板,上面有一条脱垂的回肠和与后肠相对应的第二个小孔。在盲肠板的下部,可以看到两个半阴道和半阴道,但在连接两半盲肠的膀胱板桥的上部。每个半阴道都与半子宫相连,并有自己的输卵管和卵巢。膀胱位于盲肠板的两侧,在中线处相连,呈新月形,凹面朝向头侧。基因检测证实其核型为 XX。在出生后第 5 天,患者接受了脐膨出修补术和腹壁闭合术、盲板管化术和结肠末端造口术。此外,还将半阴道和半阴道移至正位,并将膀胱板连接在一起,用于覆盖部分腹壁缺损。她于第 42 天出院,体重为 2.72 千克。她继续在门诊接受随访。结论在本病例中观察到的生殖道位置高于膀胱外翻的情况以前从未描述过,目前的 OEIS 发展理论也不能完全解释这种情况。
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CiteScore
0.60
自引率
25.00%
发文量
348
审稿时长
15 days
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