• Medicine · Feb 2022

    Case Reports

    Congenital aphallia associated with congenital urethrorectal fistula: A rare case report.

    • Si-Si Luo, Zhe Yang, Ning Ma, Wei-Xin Wang, Sen Chen, Qi Wu, Si-Wei Qu, and Yang-Qun Li.
    • 2th Department, Plastic Surgery Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
    • Medicine (Baltimore). 2022 Feb 18; 101 (7): e28878e28878.

    RationaleAphallia is an extremely rare congenital malformation of unknown cause, with few reports in the literature. It is usually associated with other urogenital and gastrointestinal anomalies and is believed to be a result of either the absence of a genital tubercle or chromosome polymorphism. Herein, we describe an extremely rare case of congenital aphallia with congenital urethrorectal fistula and describe our treatment for this patient.Patient ConcernsAn 8-year-old boy was brought to our hospital by his parents because of congenital absence of the penis. The child was male per karyotype and had excess heterochromatin on chromosome 9 (46 XY with 9 qh+). No urethral orifice was identified, and urine passed rectally since birth; thus, urinary tract outlet obstruction led to urine reflux from the anus to the epididymis for a long time. The boy had to be placed on prophylactic antibiotics because he developed urinary tract infection and epididymitis almost every day.DiagnosisCongenital aphallia (46 XY normal male karyotype) associated with congenital urethroretal fistula.InterventionsWe performed urethral exteriorization via perineal urethroplasty and urethrorectal fistula repair. The parents approved for phallic reconstruction when the boy reached puberty.OutcomeA new external urethral orifice was created on the lower scrotum. The urinary reflux was corrected, and the epididymitis symptoms disappeared. The urethral fistula was then closed. At 8 months follow up, the patient was no longer on antibiotics and had no symptoms of urinary tract infection or epididymitis.ConclusionsCompatible treatment should be adopted to address urinary tract drainage and infection. Management requires a stepwise approach to address needs as they arise. Neophalloplasty should be performed by an experienced team in early adolescence.Copyright © 2022 the Author(s). Published by Wolters Kluwer Health, Inc.

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