Congenital occlusion of ureteropelvic junction
ICD-10 Q62.11 is a billable code used to indicate a diagnosis of congenital occlusion of ureteropelvic junction.
Congenital occlusion of the ureteropelvic junction (UPJ) is a condition characterized by a blockage at the junction where the ureter meets the renal pelvis. This malformation can lead to hydronephrosis, which is the swelling of a kidney due to a build-up of urine. In pediatric patients, UPJ obstruction is one of the most common causes of renal obstruction and can present with symptoms such as abdominal pain, urinary tract infections, or failure to thrive. Diagnosis is typically made through imaging studies such as ultrasound or CT scans, which reveal the degree of obstruction and any associated renal anomalies. Treatment often involves surgical intervention to relieve the obstruction and restore normal urinary flow. The condition may be associated with other congenital malformations of the urinary system, including renal agenesis, polycystic kidney disease, bladder exstrophy, and posterior urethral valves, necessitating comprehensive evaluation and management.
Detailed history of urinary symptoms, growth parameters, and imaging results.
Pediatric patients presenting with abdominal pain or urinary tract infections.
Consideration of growth and development milestones in the context of renal function.
Family history of congenital anomalies, genetic testing results, and counseling notes.
Patients with multiple congenital anomalies requiring genetic evaluation.
Understanding the genetic syndromes associated with urinary tract malformations.
Used in surgical correction of UPJ obstruction in pediatric patients.
Operative report detailing the procedure and findings.
Pediatric urology specialists should provide detailed surgical notes.
Common symptoms include abdominal pain, urinary tract infections, and failure to thrive in infants. Diagnosis is often made through imaging studies.
