# A Case Report of Patent Urachus With Perinatal Cardiac Abnormality

**Authors:** Hanan Mohammed Alzahrani

PMC · DOI: 10.1002/ccr3.70626 · Clinical Case Reports · 2025-07-08

## TL;DR

A newborn girl with a rare patent urachus and a heart defect was successfully treated with surgery.

## Contribution

This case report highlights the successful surgical management of a rare patent urachus with perinatal cardiac abnormality.

## Key findings

- Fluoroscopic cystogram confirmed a patent urachus with leakage at the umbilical site.
- Surgical removal of the urachus led to a stable postoperative recovery.
- Early diagnosis and intervention are critical for favorable outcomes in such cases.

## Abstract

Patent urachus is a rare urachal anomaly. This case involves a newborn female with a cyst near the umbilicus and a small patent ductus arteriosus with left‐to‐right shunting. A low‐dose fluoroscopic cystogram revealed contrast entering a tubular structure extending from the bladder to the umbilicus, with evidence of leakage at the umbilical site, confirming a patent urachus. Surgical treatment was performed through an infraumbilical incision to remove the persistent urachus up to the bladder. The patient recovered well postoperatively and was discharged in stable condition to her parents' care. Early diagnosis and management are essential for favorable outcomes in such anomalies.

## Linked entities

- **Diseases:** patent urachus (MONDO:0018551), patent ductus arteriosus (MONDO:0011827)
- **Species:** Homo sapiens (taxon 9606)

## Full-text entities

- **Diseases:** patent ductus arteriosus (MESH:D004374), Patent Urachus (MESH:C536474), cyst (MESH:D003560), urachal anomaly (MESH:C536475), Perinatal Cardiac Abnormality (MESH:D066087)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC12238317/full.md

## References

12 references — full list in the complete paper: https://tomesphere.com/paper/PMC12238317/full.md

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Source: https://tomesphere.com/paper/PMC12238317