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Published on: September 15, 2017
Salt-losing crisis in infants-not always of adrenal origin
Bharathi Pai1, Nick Shaw, Wolfgang Högler
1Department of Endocrinology and Diabetes, Birmingham Children's Hospital, Steelhouse Lane, Birmingham, B4 6NH, UK. bharathipai@hotmail.com
Insights
Infants presenting with salt-losing crisis symptoms like hyponatremia and hyperkalemia may have pyelonephritis, not just congenital adrenal disorders. Promptly excluding kidney infection is crucial before considering endocrine causes.
Area of Science:
- Pediatric Endocrinology
- Nephrology
- Genetics
Background:
- Congenital adrenal hyperplasia is a common cause of salt-losing crisis in infants.
- Early diagnosis and treatment are vital to prevent mortality.
Observation:
- Three infants presented with vomiting, hyponatremia, and hyperkalemia, initially suspected as congenital adrenal disorders.
- Infants showed elevated plasma aldosterone and renin levels.
Findings:
- The infants' condition was attributed to pyelonephritis and structural kidney anomalies, leading to secondary aldosterone resistance.
- This highlights that kidney infections can mimic endocrine salt-losing conditions.
Implications:
- Pyelonephritis should be considered in infants with salt-losing crisis, especially outside the neonatal period.
- Excluding renal causes is essential before initiating treatment for suspected congenital adrenal disorders.
Unlabelled:
Three infants (age 1.5, 4 and 7 months) presented with vomiting, hyponatremia and hyperkalaemia suggestive of a salt-losing congenital adrenal condition. Diagnostic endocrine bloods were taken and adrenal steroid therapy was started. The infants were subsequently found to have raised plasma aldosterone and renin levels due to pyelonephritis and structural anomalies of the kidneys, demonstrating secondary aldosterone resistance.
Conclusion:
Establishing the diagnosis of congenital adrenal disorders is essential in a baby who develops a salt-losing crisis in the first few weeks of life. However, pyelonephritis should be considered and can be rapidly excluded in any infant presenting with a salt-losing crisis with hyponatremia and hyperkalaemia, in particular, outside the neonatal period. Only then should an endocrine cause for this presentation be considered and treatment commenced.
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