SURGICAL CORRECTION OF PENILE HYPOSPADIAS IN BOYS WITH INCOMPLETE URETHRAL DUPLICATION
Relevance of the problem. Hypospadias is a congenital anomaly of the male urinary system. The prevalence of hypospadias varies worldwide. The combination of hypospadias with incomplete duplicated urethra is less common.
Aim: We present a case of surgical correction of urethral anomaly in a boy with hypospadias and incomplete duplicated urethra.
Materials and methods: Patients with hypospadias and congenital incomplete duplicated urethra who underwent urethroplasty with excision of the interurethral septum were reviewed.
Results: From 2016 to 2023, six patients with incomplete duplicated urethra and different forms of primary and secondary hypospadias were operated on. In all patients, the septum between the urethras was excised, creating a common urethral tube with stenting with a Nelaton catheter. To prevent postoperative complications, urine was diverted using an epicystostomy tube and urethral catheter. No complications were observed in any of the six patients in the early and delayed postoperative period.
Conclusion: The form of hypospadias is often determined intraoperatively. Hypospadias can be accompanied by various developmental anomalies of the external genitalia and urethra.
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Clinical case
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Zharkimbayeva A.D., Kanapiyanov Zh.K., Aubakirov M.T., Dyussembayev A.A., Ten Yu.V., Lozovoy V.M., Madiyeva M.R. Surgical correction of penile hypospadias in boys with incomplete urethral duplication // Nauka i Zdravookhranenie [Science & Healthcare]. 2023, (Vol.25) 2, pp. 293-296. doi 10.34689/SH.2023.25.2.038Related publications:
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