Surgical Management of Diphallia in a 10-Year-Old Child with a Congenital Anomaly: A Case Report
DOI:
https://doi.org/10.58342/ghalibMj.V.2.I.1.13Keywords:
Diphallia, Congenital Anomaly, Corrective SurgeryAbstract
Background/introduction: Diphallia is one of the rarest congenital anomalies in males, resulting in duplication of the external genitalia. Although treatment typically involves surgical intervention, each case presents unique complexities. This article provides a detailed case report of diphallia in a 10-year-old boy and its surgical management.
Case presentation: The patient presented with two glans penises under the prepuce. Urological investigations revealed a functional complete right-sided urethra, while the left urethra was incomplete. Surgical correction included separating the urethras and creating a single functional channel, along with amputation of the left glans due to its incomplete functionality and aesthetic concerns.
Conclusion: Postoperative outcomes demonstrated full recovery of urinary function and acceptable aesthetic results. This case underscores the importance of early diagnosis, precise evaluation, and appropriate surgical interventions in managing congenital anomalies.
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