# Case Report: Diagnostic overlap of OHVIRA syndrome and Gartner duct cyst: challenges in imaging and management

**Authors:** Junfeng Zhao, Yaqing Bao, Linglu Gong, Zhan Shi, Xiaoqiang Chen, Yan Li

PMC · DOI: 10.3389/fped.2025.1536314 · Frontiers in Pediatrics · 2025-05-22

## TL;DR

This case report highlights the difficulty in distinguishing OHVIRA syndrome from Gartner duct cyst in prepubertal girls using imaging techniques.

## Contribution

The study presents two cases showing diagnostic overlap between OHVIRA syndrome and Gartner duct cyst due to similar imaging features.

## Key findings

- Both cases showed unilateral renal agenesis and cystic lesions near the bladder on CT and MRI.
- Diagnostic challenges arose due to overlapping embryologic origins and imaging findings between the two conditions.

## Abstract

This case series explores the diagnostic overlap between OHVIRA syndrome (obstructed hemivagina and ipsilateral renal anomaly) and Gartner duct cyst (GDC) with ipsilateral renal dysplasia in two prepubertal girls. Both cases exhibited similar imaging features on CT and MRI—including unilateral renal agenesis, ectopic ureter with abnormal insertion, cystic lesions posterolateral to the bladder— which led to significant diagnostic challenges. Despite differing in pathology, the overlap in embryologic origins and imaging findings made differentiation difficult. This series underscores the importance of comprehensive imaging and a multidisciplinary approach for accurate diagnosis. Current management strategies are discussed, highlighting the need for individualized treatment plans in prepubertal patients with complex genitourinary anomalies.

## Linked entities

- **Diseases:** OHVIRA syndrome (MONDO:0008636)

## Full-text entities

- **Diseases:** ipsilateral renal anomaly (MESH:C535986), GDC (MESH:D015529), ectopic ureter (MESH:D014516), unilateral renal agenesis (MESH:D000075529), cystic (MESH:D018297), genitourinary anomalies (MESH:D014564), obstructed hemivagina (MESH:D000402), renal dysplasia (MESH:C537580), OHVIRA syndrome (MESH:D013577)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12139208/full.md

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12139208/full.md

## References

13 references — full list in the complete paper: https://tomesphere.com/paper/PMC12139208/full.md

---
Source: https://tomesphere.com/paper/PMC12139208