Life-Threatening Hyponatremia, Hyperkalemia, and Shock in Infancy: Not Always Congenital Adrenal Hyperplasia

Hyponatremia and hyperkalemia, though uncommon in infancy, are potentially life-threatening electrolyte disturbances. We discuss a case of secondary pseudohypoaldosteronism (PHA) in a six-month-old male presenting with recurrent vomiting, severe hyponatremia (119 mmol/L), hyperkalemia (6.6 mmol/L), and metabolic acidosis (bicarbonate: 9 mmol/L). The patient's condition rapidly deteriorated with hypotension and respiratory distress requiring intensive care and mechanical ventilation. Investigations identified an Escherichia coli urinary tract infection (UTI), and further laboratory tests revealed markedly elevated serum renin and aldosterone levels, consistent with secondary PHA associated with UTI in infancy. This report explores the incidence, proposed pathophysiology, and management strategies for secondary PHA. Additionally, we provide information to aid in differentiating among the potential causes of similar biochemical abnormalities, including congenital adrenal hyperplasia (CAH), in pediatric patients.

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Publication Details

Journal
Cureus
Published
2025-08-03
DOI
https://doi.org/10.7759/cureus.89285
Primary Topic
Ion Transport and Channel Regulation
Type
article
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article

Life-Threatening Hyponatremia, Hyperkalemia, and Shock in Infancy: Not Always Congenital Adrenal Hyperplasia

Kwai Yu Winnie Chan, Chon In Kuok, Wen‐Kuei Chung
Cureus
Ion Transport and Channel Regulation
article

Life-Threatening Hyponatremia, Hyperkalemia, and Shock in Infancy: Not Always Congenital Adrenal Hyperplasia

Kwai Yu Winnie Chan, Chon In Kuok, Wen‐Kuei Chung
article en

Abstract

Hyponatremia and hyperkalemia, though uncommon in infancy, are potentially life-threatening electrolyte disturbances. We discuss a case of secondary pseudohypoaldosteronism (PHA) in a six-month-old male presenting with recurrent vomiting, severe hyponatremia (119 mmol/L), hyperkalemia (6.6 mmol/L), and metabolic acidosis (bicarbonate: 9 mmol/L). The patient's condition rapidly deteriorated with hypotension and respiratory distress requiring intensive care and mechanical ventilation. Investigations identified an Escherichia coli urinary tract infection (UTI), and further laboratory tests revealed markedly elevated serum renin and aldosterone levels, consistent with secondary PHA associated with UTI in infancy. This report explores the incidence, proposed pathophysiology, and management strategies for secondary PHA. Additionally, we provide information to aid in differentiating among the potential causes of similar biochemical abnormalities, including congenital adrenal hyperplasia (CAH), in pediatric patients.

CureusVol. 17(8)
Queen Elizabeth Hospital (GB), Queen Elizabeth Hospital (CN)
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Openalex Percentile: Top 83%
Ion Transport and Channel Regulation
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