# Herlyn Werner Wunderlich Syndrome with Hydrocolpos: A Case Report

**Authors:** Saurav Sen Oli, Shova Sapkota, Rupa Bajagain, Rachana Saha, Suman Paudel

PMC · DOI: 10.31729/jnma.8520 · JNMA: Journal of the Nepal Medical Association · 2024-03-31

## TL;DR

This case report describes a rare urogenital disorder in a 14-year-old girl, diagnosed and treated successfully with surgery.

## Contribution

The paper presents a new clinical case of Herlyn-Werner-Wunderlich Syndrome with hydrocolpos and its surgical management.

## Key findings

- Ultrasound confirmed Herlyn-Werner-Wunderlich Syndrome in a 14-year-old girl with right flank pain.
- Surgical drainage and marsupialization resolved the condition with no complications after two weeks.
- Timely diagnosis and treatment are critical to prevent gynecological complications.

## Abstract

Herlyn-Werner-Wunderlich Syndrome is a very rare congenital malformation of the urogenital tract involving both the Mullerian and Wolffian ducts characterized by the triad uterine diadelphys, obstructed vagina, and unilateral renal agenesis. If not diagnosed on time it may progress to adverse gynecological complications making timely diagnosis and treatment crucial. We hereby present a 14-year girl with right flank pain diagnosed as Herlyn-Werner-Wunderlich Syndrome by ultrasound scan which was managed surgically with drainage of hydrocolpos and marsupialization of vaginal septum. On two weeks follow up patient had symptomatic improvement with no any complications.

## Full-text entities

- **Diseases:** uterine diadelphys (MESH:D014591), Herlyn-Werner-Wunderlich Syndrome (MESH:D014898), flank pain (MESH:D021501), Hydrocolpos (MESH:D052202), vagina (MESH:D014625), gynecological complications (MESH:D005831), unilateral renal agenesis (MESH:D000075529), congenital malformation of the urogenital tract (MESH:D014564)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC10924486/full.md

## References

11 references — full list in the complete paper: https://tomesphere.com/paper/PMC10924486/full.md

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Source: https://tomesphere.com/paper/PMC10924486