Other congenital malformations of ureter
ICD-10 Q62.8 is a billable code used to indicate a diagnosis of other congenital malformations of ureter.
Congenital malformations of the ureter can encompass a variety of structural abnormalities that may affect the normal function of the urinary system. These malformations can include conditions such as ureteral duplication, ectopic ureters, and ureteral stenosis. In pediatric patients, these anomalies can lead to significant complications, including urinary obstruction, recurrent urinary tract infections, and renal impairment. For instance, renal agenesis, where one or both kidneys fail to develop, can be associated with ureteral anomalies. Polycystic kidney disease, characterized by the formation of cysts in the kidneys, may also present with ureteral malformations. Bladder exstrophy, a condition where the bladder is exposed outside the body, often coexists with ureteral defects. Posterior urethral valves, a condition where abnormal tissue obstructs the urethra, can lead to hydronephrosis and renal damage, necessitating careful monitoring and intervention. Accurate coding of these conditions is essential for appropriate management and treatment planning.
Pediatric documentation should include detailed descriptions of the malformation, associated symptoms, and any interventions performed. Growth and developmental assessments are also critical.
Common scenarios include newborns presenting with hydronephrosis, children with recurrent UTIs, and cases requiring surgical intervention for ureteral anomalies.
Consideration must be given to the age of the patient and the potential for growth-related changes in the urinary system.
Genetic documentation should include family history, genetic testing results, and any syndromic associations with congenital malformations.
Scenarios may involve genetic counseling for families with a history of congenital urinary tract anomalies or syndromes associated with renal malformations.
Geneticists should be aware of the potential for chromosomal abnormalities that may present with urinary tract malformations.
Used in cases of ureteral malformations requiring surgical correction.
Surgical reports detailing the procedure and indications.
Pediatric urologists should ensure accurate coding based on the specific malformation addressed.
Common congenital malformations include ureteral duplication, ectopic ureters, and ureteral stenosis. These conditions can lead to significant urinary tract complications and require careful management.
