- Research Article
- 10.4293/crsls.2025.00109
Diagnostic Challenges and Management of Urachal Malformations in an Infant
- Dec 19, 2025
- CRSLS : MIS Case Reports from SLS
- Ahmed Osama Hassan + 3 more +3
Background:The urachus is a vestigial remnant of the allantois which naturally degenerates after birth. Failure of closure of the urachus can result in urachal malformations, with the most common being a urachal cyst. Diagnosing a urachal cyst is challenging due to its diverse presentations, often leading to misdiagnosis. Although they are often asymptomatic, urachal cysts can be significant because they can lead to complications.Case Report:We report a late preterm male infant born at 36 weeks + 5 days, in whom an antenatal anomaly scan revealed a unilocular intra-abdominal cyst adjacent to the bladder. Postnatal ultrasound kidney, ureter, and bladder (KUB) at 3 days of age demonstrated a cystic structure anterior and superior to the bladder, accompanied by mild bilateral hydronephrosis. A voiding cystourethrogram (VCUG) at 2 weeks revealed a cystic mass connected to the bladder by a fistulous tract, raising differential diagnoses of urachal cyst, bladder diverticulum, or incomplete bladder duplication. At 2 months, diagnostic cystoscopy and laparoscopy were performed. Cystoscopy showed a small opening at the bladder dome, while laparoscopy identified a 5 × 5-cm cyst extending from the bladder dome to the umbilicus. The cyst was excised laparoscopically, and bladder repair was completed. Histopathology revealed benign urothelium with mild chronic inflammation and a muscular wall, suggestive of a urachal diverticulum. Postoperative recovery was uneventful, and follow-up imaging demonstrated normal bladder morphology and renal function.Conclusions:Our case supports the efficacy of diagnostic and therapeutic laparoscopy in accurately diagnosing urachal anomalies, aiding in treatment decisions, and preventing future complications.
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