Management of complicated ureteroceles: Different modalities of treatment and long-term outcome
Sujit K Chowdhary1, Deepak K Kandpal1, Anupam Sibal1
1Department of Pediatric Urology and Pediatric Surgery, Indraprastha Apollo Hospitals, Sarita Vihar, New Delhi, India.
Insights
Ureteroceles, rare in India, can cause severe urinary complications if untreated in childhood. This study details the management of 36 pediatric cases, emphasizing individualized treatment plans for better outcomes.
Area of Science:
- Pediatric Urology
- Congenital Abnormalities
- Obstructive Uropathy
Background:
- Ureteroceles are rare congenital anomalies, with limited reporting from India.
- They can be detected antenatally or present later with obstructive uropathy complications.
- Delayed diagnosis and treatment in childhood can lead to severe adult complications.
Observation:
- A series of 36 consecutive pediatric patients with ureteroceles were managed between 2003-2013.
- Investigations included ultrasound, micturating cystourethrogram, and isotope renogram.
- Management varied from observation for asymptomatic cases to endoscopic deroofing and stenting for symptomatic ones.
Findings:
- Six patients presented with acute complications requiring individualized management.
- A fixed protocol for investigation and operative intervention was applied.
- Asymptomatic, unobstructed ureteroceles were managed conservatively.
Implications:
- This study provides a comprehensive report on ureterocele management in Indian children.
- Highlights the importance of early diagnosis and tailored treatment strategies.
- Emphasizes the potential for severe complications if ureteroceles are missed in early life.
Abstract:
The presentation and management of ureterocele has been rarely reported from India and is limited to an odd case report. They can be detected antenatally, may have incidental diagnosis or present with consequences of obstructive uropathy. They always present with secondary complications in adulthood, if the diagnosis and treatment is missed in early years of life. The natural history may be particularly disastrous in cases of bilateral obstructing ureterocele. The complications secondary to obstructive ureterocele can be urinary retention, pyonephrosis, urosepsis, stones and even chronic renal failure. Each of these patients needs an individualized treatment plan. In the period 2003-2013, we managed 36 consecutive patients with varied presentation of this entity. All were managed on the basis of a fixed protocol of investigation and operative intervention. Ultrasound, micturating cystourethrogram, isotope renogram were done preoperatively in all the babies. Those with asymptomatic, unobstructed ureteroceles were left without any intervention. Simple or complex intravesical ureteroceles underwent examination under anesthesia and endoscopic deroofing and DJ stenting for 3 weeks. Of a total of 36 children, 6 were presented with acute complications of ureterocele. They have been managed on an individualized optimum management plan. Their management approach with follow-up is being reported as there is no previous reported series on ureterocele in children from our country.
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