Childhood urolithiasis is an evolving condition with an increasing incidence and prevalence over the last 2 decades. Over that time the underlying cause has shifted from predominantly infectious to metabolic in nature. This review describes the pathophysiology, underlying metabolic abnormalities, clinical presentation, evaluation, and management of childhood urolithiasis. A comprehensive metabolic evaluation is essential for all children with renal calculi, given the high rate of recurrence and the importance of excluding inherited progressive conditions.
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The incidence and prevalence of childhood urolithiasis has been increasing over the last decade.
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The majority of renal calculi in children are comprised of either calcium oxalate or calcium phosphate and are often associated with a metabolic abnormality.
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Idiopathic hypercalciuria and hypocitraturia are the most frequently reported metabolic abnormalities.
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Given the high risk of recurrences in children with idiopathic hypercalciuria and hypocitraturia and the importance of excluding rare but treatable conditions such as primary hyperoxaluria and cystinuria a comprehensive metabolic evaluation is indicated in all children.
Introduction
Urolithiasis is a fairly common disease in adults with an estimated prevalence of 3% to 5%. In economically developed countries, urolithiasis has been regarded as an uncommon condition in children. The estimated incidence in the United States from the 1950s to the 1970s is approximately 1% to 2% that of adults. More recent studies from the United States suggest an increase in the incidence and prevalence, with one study demonstrating a nearly 5-fold increase in the incidence in the last decade. Reports regarding gender predisposition have varied, with some studies suggesting equal prevalence and others indicating a greater risk among boys. Race and geography seem to play a vital role in the prevalence and cause of pediatric stone disease. In certain regions, such as Southeast Asia, the Middle East, India, and Pakistan, calculi are endemic. Calculi are particularly uncommon in children of African descent. The endemic calculi observed in developing nations are often confined to the bladder and comprise predominantly ammonium acid, urate, and uric acid, and seem to correlate with a decreased availability of dietary phosphates. In the United States, urolithiasis seems to be more common in Caucasian children from the Southeastern region. Over the last 3 decades the cause of childhood urolithiasis in the United Kingdom has shifted from predominantly infectious to metabolic in nature. Most calculi in the United States are found in the kidneys or ureters, comprise either calcium oxalate or calcium phosphate, and often associated with a metabolic abnormality.