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Reversible secondary pseudohypoaldosteronism due to pyelonephritis
Kenichi Maruyama1, Hiroyuki Watanabe, Kazumichi Onigata
1Division of Nephrology, Gunma Children's Medical Center, 779 Shimohakoda, Hokkitsu, Gunma 377-8577, Japan. maru@gcmc.pref.gunma.jp
Pediatric Nephrology (Berlin, Germany)
|December 13, 2002
Abstract:
We report a 5-week-old boy who developed severe hyponatremia and hyperkalemia secondary to acute pyelonephritis. The patient presented with non-specific signs, including poor appetite, failure to thrive, and dehydration. An endocrinological evaluation led to a diagnosis of pseudohypoaldosteronism. The patient had phimosis, but no congenital urinary tract malformations. Outflow obstruction secondary to the phimosis appears to have caused pyelonephritis, and renal inflammation decreased responsiveness to aldosterone transiently.