Hyponatremic hypertensive syndrome in pediatric patients: is it really so rare?

Yael Kovalski1, Roxana Cleper, Irit Krause

  • 1Institute of Pediatric Nephrology, Schneider Children's Medical Center of Israel, Petach Tikva, 49202, Israel.

Insights

Hyponatremic hypertensive syndrome (HHS) in children presents with polyuria, polydipsia, and hypertension. Timely diagnosis and percutaneous angioplasty can cure this condition, suggesting it may be more common than previously recognized.

Area of Science:

  • Pediatric Nephrology
  • Cardiovascular Research
  • Endocrinology

Background:

  • Hyponatremic hypertensive syndrome (HHS) involves unilateral renal artery stenosis, leading to secondary hypertension and renal dysfunction via hyperfiltration and renin-angiotensin system (RAS) activation.
  • Understanding the pathophysiology of HHS is crucial for diagnosing and managing pediatric hypertension.
  • The renin-angiotensin system plays a key role in the development of hypertension in HHS.

Observation:

  • Four pediatric cases of HHS are presented, exhibiting polyuria, polydipsia, electrolyte imbalances, metabolic alkalosis, and nephrotic-range proteinuria.
  • In one case, glomerular and tubular abnormalities were observed preceding the onset of hypertension.
  • Clinical presentation of HHS can be variable, including significant renal dysfunction.

Findings:

  • Successful treatment of renal ischemia via percutaneous angioplasty led to the resolution of all HHS symptoms in the described cases.
  • Percutaneous angioplasty is an effective treatment for correcting the underlying cause of HHS.
  • Complete recovery from HHS is achievable with appropriate intervention.

Implications:

  • HHS may be underdiagnosed in the pediatric population.
  • Clinicians should maintain a high index of suspicion for HHS in children presenting with relevant symptoms.
  • Early diagnosis and prompt treatment of renal artery stenosis can lead to a cure for HHS.
Abstract

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