# Complete Diphallia With Associated Epispadias: A Rare Congenital Anomaly Diagnosed in Adulthood

**Authors:** Shuvo Khandokar, Sabrin Islam

PMC · DOI: 10.7759/cureus.103891 · Cureus · 2026-02-19

## TL;DR

A 24-year-old man was diagnosed with diphallia, a rare condition involving penile duplication, highlighting its unusual presentation in adulthood.

## Contribution

This case report presents a rare instance of diphallia diagnosed in adulthood, emphasizing individualized management.

## Key findings

- Diphallia was diagnosed in a 24-year-old male without prior complications.
- The case highlights the variability in diphallia presentations and the need for tailored treatment approaches.

## Abstract

Diphalia is an extremely rare urogenital condition presenting with penile duplication. Although it is typically diagnosed in the neonatal period due to associated congenital anomalies, some cases may present late without any related complications. Every case of diphallia presents a distinct set of symptoms and associations. In this case report, we underscore an interesting clinical presentation of diphallia in a 24-year-old male and the significance of individualized management of the condition.

## Linked entities

- **Diseases:** diphallia (MONDO:0016416)

## Full-text entities

- **Diseases:** Complete Diphallia (MESH:D001766), penile duplication (MESH:D010409), Epispadias (MESH:D004842), Congenital Anomaly (MESH:D000013)

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13005225/full.md

## References

9 references — full list in the complete paper: https://tomesphere.com/paper/PMC13005225/full.md

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Source: https://tomesphere.com/paper/PMC13005225