ArticleUrology case reports2026
Prolapsed ureterocele in a new-born female: A rare presentation of duplex kidney anomaly with diagnostic challenges.
Article in Urology case reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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8 authors.
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Abstract
Ureterocele is a congenital dilatation of the distal ureter. Although typically diagnosed prenatally or incidentally, prolapsed ureterocele in a neonate is rare. We report a 13-day-old female infant referred for evaluation of a vulvar mass initially taken for hymeneal imperforation. Prenatal history was unremarkable. Physical examination revealed a reddish vulvar mass with whitish secretions. Pelvic ultrasound demonstrated a duplicated right renal system with a ureterocele, suggesting a prolapsed ureterocele. Incision then differed ureterocele resection was performed without complications. Prolapsed ureterocele in neonates is a rare but important differential diagnosis for interlabial masses. Early recognition and surgical management preserve renal function.
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