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2025 ICD-10-CM code Q62.2

Congenital megaureter. Congenital dilatation of ureter.

Use additional codes to specify any associated conditions, such as hydronephrosis (N13.30) or vesicoureteral reflux (N13.7).If the megaureter is unilateral, specify the affected side using laterality codes.

Medical necessity for intervention is established by demonstrating the impact of the megaureter on kidney function or the patient's overall health.Recurrent urinary tract infections, evidence of obstruction, or deterioration of renal function can justify the need for surgical repair or other management strategies.

Diagnosis and management of congenital megaureter typically falls under the purview of pediatric urologists or nephrologists.They are responsible for evaluating the severity of the condition, monitoring kidney function, and determining the appropriate course of treatment, which may range from observation to surgical intervention.

In simple words: Megaureter is a birth defect where one or both of the tubes that carry urine from the kidneys to the bladder are wider than normal.

A congenital condition characterized by an abnormally dilated ureter. This dilatation is typically due to a developmental defect and can occur unilaterally or bilaterally.

Example 1: A newborn infant is found to have a dilated ureter on ultrasound during a prenatal checkup. Postnatal evaluation confirms the diagnosis of congenital megaureter., A toddler presents with recurrent urinary tract infections. Imaging studies reveal a significantly dilated ureter, leading to a diagnosis of congenital megaureter., A teenager undergoes imaging for abdominal pain and is incidentally found to have a mildly dilated ureter, consistent with congenital megaureter, which has remained asymptomatic until now.

Documentation should include imaging studies (such as ultrasound, VCUG, or CT scan) demonstrating the dilated ureter, as well as any associated findings like hydronephrosis or renal dysplasia.Details of the patient's clinical presentation, including any symptoms like urinary tract infections or abdominal pain, should also be documented.If surgical intervention is performed, operative reports and post-operative follow-up notes are essential.

** Congenital megaureter should be distinguished from other causes of ureteral dilatation, such as obstruction from a stone or tumor. It's important to accurately document the congenital nature of the condition to ensure appropriate coding and management.

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