Pediatric Urology

Hypospadias
A congenital anomaly where the urethral opening is located on the underside of the penis, affects approximately 1 in 250 male newborns. Surgical correction, typically performed between 6 and 18 months, involves reconstructing the urethra to achieve normal function and appearance. Techniques like the tubularized incised plate (TIP) repair offer high success rates, with complication rates below 10% in experienced hands. Pediatric urologists must balance functional outcomes with cosmetic results, as psychological impacts can persist into adulthood. Long-term follow-up is essential to monitor for complications like fistulae or strictures.
Pelvi-ureteric junction obstruction
A blockage at the junction of the renal pelvis and ureter, can cause hydronephrosis and progressive renal damage. It is often detected prenatally via ultrasound. Management depends on severity; mild cases may resolve spontaneously, while significant obstruction requires surgical intervention. Pyeloplasty, often performed laparoscopically or robotically, is the gold standard, with success rates exceeding 95%. Minimally invasive approaches reduce recovery time and scarring, critical for pediatric patients. Regular imaging post-surgery ensures preserved renal function.
Undescended test
Undescended test is (cryptorchidism), affecting 3-5% of full-term male infants, poses risks of infertility and testicular cancer if untreated. Orchiopexy, the surgical fixation of the testis in the scrotum, is recommended between 6 and 12 months to optimize fertility potential. Laparoscopic orchiopexy is effective for intra-abdominal testes, offering diagnostic and therapeutic benefits. Early intervention reduces malignancy risk, though lifelong self-examination is advised. Parental education is crucial to address concerns about fertility and cosmetic outcomes.