Prenatal ultrasonographic features of persistent urogenital sinus with hydrometrocolpos and ascites
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作者:
Gul, Ahmet
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Istanbul Bakirkoy Women & Children Hosp, Dept Obstet & Gynecol, Maternal & Fetal Unit, Istanbul, TurkeyIstanbul Bakirkoy Women & Children Hosp, Dept Obstet & Gynecol, Maternal & Fetal Unit, Istanbul, Turkey
Gul, Ahmet
[1
]
Yildirim, Gokhan
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Istanbul Bakirkoy Women & Children Hosp, Dept Obstet & Gynecol, Maternal & Fetal Unit, Istanbul, TurkeyIstanbul Bakirkoy Women & Children Hosp, Dept Obstet & Gynecol, Maternal & Fetal Unit, Istanbul, Turkey
Yildirim, Gokhan
[1
]
Gedikbasi, Ala
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Istanbul Bakirkoy Women & Children Hosp, Dept Obstet & Gynecol, Maternal & Fetal Unit, Istanbul, TurkeyIstanbul Bakirkoy Women & Children Hosp, Dept Obstet & Gynecol, Maternal & Fetal Unit, Istanbul, Turkey
Gedikbasi, Ala
[1
]
Gungorduk, Kemal
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Istanbul Bakirkoy Women & Children Hosp, Dept Obstet & Gynecol, Maternal & Fetal Unit, Istanbul, TurkeyIstanbul Bakirkoy Women & Children Hosp, Dept Obstet & Gynecol, Maternal & Fetal Unit, Istanbul, Turkey
Gungorduk, Kemal
[1
]
Ceylan, Yavuz
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Istanbul Bakirkoy Women & Children Hosp, Dept Obstet & Gynecol, Maternal & Fetal Unit, Istanbul, TurkeyIstanbul Bakirkoy Women & Children Hosp, Dept Obstet & Gynecol, Maternal & Fetal Unit, Istanbul, Turkey
Ceylan, Yavuz
[1
]
机构:
[1] Istanbul Bakirkoy Women & Children Hosp, Dept Obstet & Gynecol, Maternal & Fetal Unit, Istanbul, Turkey
Objective Hydrometrocolpos is a rare congenital disorder very rarely reported on prenatal sonography. In this study we report a persisten urogenital sinus with hydrometrocolpos and ascites at 24 weeks of gestation. Case Detailed ultrasonographic examination revealed female fetus with pelvic mass measured as 60 x 70 x 80 mm, anterior to sacral bone and inferior to bladder, and ascites, ureterocele, hydoureters, hydronephrosis but normal amniotic fluid. Further examination showed that cervical canal and uterin cavity was in continuation with the pelvic mass and dilatation of uterine tubes implicated hydrometrocolpos. Physical examination of the neonate revealed a single anterior opening at perineum and a patent anus but no visible urethral orifice. A voiding cystourethrogram demonstrated a urethrovaginal fistula. The neonate underwent ureteroneoostomy and was discharged on day 10 for follow-up and final repair. Conclusion Prenatal ultrasonographic diagnosis of hydrometrocolpos in our case prevented unnecessary interventions and allowed early neonatal treatment.