Abstract
Congenital megaprepuce is a rare condition leading to micturition problems with excessive ballooning in the postnatal period with unknown etiology. Congenital adrenal hyperplasia, cystic and tumoral diseases should be considered in the differential diagnosis of congenital megaprepuce. A 2-month-old male patient was admitted to our hospital with penile anomaly. Phimosis, penile oedema and megaprepuce were noticed on physical examination. Elective surgery was recommended by the pediatric urology department. We present an isolated congenital megaprepuce case that underwent successful reconstructive surgery.
Keywords: Congenital abnormalities, Foreskin, Penis, Surgery
Copyright and license
Copyright © 2013 The Author(s). This is an open access article distributed under the Creative Commons Attribution License (CC BY), which permits unrestricted use, distribution, and reproduction in any medium or format, provided the original work is properly cited.