Fetal urinary ascites caused by bladder rupture due to paraurethral cyst: a rare case

Fetal urinary ascites is an uncommon prenatal finding most often associated with lower urinary tract obstruction (LUTO). We report a rare case of fetal urinary ascites caused by bladder rupture secondary to suspected urethral compression by a paraurethral cyst. A 26-year-old gravida 3 para 1 woman was referred at 32 weeks' gestation due to newly detected isolated fetal ascites and mild polyhydramnios. Detailed ultrasonography suggested bladder wall defect and a cystic structure adjacent to the right inguinal canal. Fetal MRI confirmed bladder rupture and supported the suspicion of LUTO. Conservative management was adopted due to stable fetal condition and preserved renal appearance. The ascites resolved spontaneously before delivery. A healthy female neonate was born at term, and the paraurethral cyst resolved spontaneously postnatally. This case highlights a rare etiology of fetal urinary ascites and demonstrates that expectant management may result in favorable outcomes in selected cases.

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Publication Details

Journal
Archives of Gynecology and Obstetrics
Published
2026-04-13
DOI
https://doi.org/10.1007/s00404-026-08415-1
Primary Topic
Pediatric Urology and Nephrology Studies
Type
article
Field-Weighted Citation Impact
0.00

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article

Fetal urinary ascites caused by bladder rupture due to paraurethral cyst: a rare case

Yifat Wiener, Stanislav Kotcherov, Amit Haboosheh, Ron Maymon et al.
Archives of Gynecology and Obstetrics
Pediatric Urology and Nephrology Studies
article

Fetal urinary ascites caused by bladder rupture due to paraurethral cyst: a rare case

Yifat Wiener, Stanislav Kotcherov, Amit Haboosheh, Ron Maymon, Orna Levinsohn Tavor, Marian Pekar Zlotin
article en

Abstract

Fetal urinary ascites is an uncommon prenatal finding most often associated with lower urinary tract obstruction (LUTO). We report a rare case of fetal urinary ascites caused by bladder rupture secondary to suspected urethral compression by a paraurethral cyst. A 26-year-old gravida 3 para 1 woman was referred at 32 weeks' gestation due to newly detected isolated fetal ascites and mild polyhydramnios. Detailed ultrasonography suggested bladder wall defect and a cystic structure adjacent to the right inguinal canal. Fetal MRI confirmed bladder rupture and supported the suspicion of LUTO. Conservative management was adopted due to stable fetal condition and preserved renal appearance. The ascites resolved spontaneously before delivery. A healthy female neonate was born at term, and the paraurethral cyst resolved spontaneously postnatally. This case highlights a rare etiology of fetal urinary ascites and demonstrates that expectant management may result in favorable outcomes in selected cases.

Archives of Gynecology and ObstetricsVol. 313(1)
Hadassah Medical Center (IL), Assaf Harofeh Medical Center (IL)
Tel Aviv University
Good health and well-being
Openalex Percentile: Top 24%
Pediatric Urology and Nephrology Studies
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