Literature DB >> 30962012

Transient pseudohypoaldosteronism: a potentially severe condition affecting infants with urinary tract malformation.

X Delforge1, G Kongolo2, A Cauliez3, K Braun3, E Haraux4, P Buisson4.   

Abstract

BACKGROUND: Secondary pseudohypoaldosteronism (S-PHA) is a life-threatening condition affecting young children with urinary tract malformation (UTM).
OBJECTIVE: The aim of the study was to highlight the diagnosis of S-PHA in children with UTM and propose appropriate management. STUDY
DESIGN: The authors retrospectively reviewed cases of S-PHA related to UTM observed at the institution and searched the PubMed® database to review the literature.
RESULTS: A total of 116 cases of S-PHA associated with UTM, including the four cases from the institution, were reviewed. One hundred six cases (92.2%) were younger than 6 months, and 95 cases (81.9%) occurred in boys. Urinary tract infection was associated in 105 cases (90.5%). All types of UTM were observed. In the absence of urinary tract infection, S-PHA was related to bilateral UTM or solitary kidney. In 89 cases (76.5%), S-PHA resolved with medical treatment only. In cases of UTM requiring immediate surgery, electrolyte imbalance related to S-PHA also resolved after surgery. Children with associated urinary tract infection and bilateral UTM are at higher risk of developing S-PHA. DISCUSSION: The pathogenesis of S-PHA has not been fully elucidated. Renal tubular immaturity may be one of the factors involved, in view of the young age of the population being affected. A high rate of bilateral UTM (or UTM on solitary kidney) was observed (50.9%), suggesting an association with S-PHA. In the absence of urinary tract infection (UTI), S-PHA appeared to occur more frequently in the presence of bilateral UTM. Although the indication for early surgery remains unclear, it may have a role in the prevention of UTI and prevention of recurrence of S-PHA. Serum electrolytes should be checked in children with UTM before urological surgery, and/or presenting urinary tract infection, before the age of 6 months. The results of this study must be interpreted cautiously because of its retrospective nature and the fact that data were derived from various articles. Few articles on S-PHA related to UTM have been published in the literature. To the best of the authors' knowledge, the study constitutes the largest series published to date.
CONCLUSIONS: S-PHA results in potentially severe electrolyte imbalance and affects children younger than 6 months with UTI and/or UTM. Electrolyte abnormalities related to S-PHA often resolve after administration of appropriate intravenous electrolyte solution and treatment of UTI and/or surgery.
Copyright © 2019 Journal of Pediatric Urology Company. Published by Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Hyperaldosteronism; Hyperkalemia; Hyponatremia; Pseudohypoaldosteronism; Urinary tract infection; Urinary tract malformation

Mesh:

Year:  2019        PMID: 30962012     DOI: 10.1016/j.jpurol.2019.03.002

Source DB:  PubMed          Journal:  J Pediatr Urol        ISSN: 1477-5131            Impact factor:   1.830


  3 in total

1.  Case Report: A Novel Compound Heterozygote Mutation of the SCNN1B Gene Identified in a Chinese Familial Pseudohypoaldosteronism Disease Type I With Persistent Hyperkalemia.

Authors:  Zongzhi Liu; Xiaojiao Wang; Zilong Zhang; Zixin Yang; Junyun Wang; Yajuan Wang
Journal:  Front Pediatr       Date:  2022-03-10       Impact factor: 3.418

2.  Transient pseudohypoaldosteronism in infancy mainly manifested as poor appetite and vomiting: Two case reports and review of the literature.

Authors:  Yueerlanmu Tuoheti; Yucan Zheng; Yan Lu; Mei Li; Yu Jin
Journal:  Front Pediatr       Date:  2022-08-25       Impact factor: 3.569

3.  Neonatal Pseudohypoaldosteronism Type-1 in Japan.

Authors:  Kazumichi Fujioka; Ruka Nakasone; Kosuke Nishida; Mariko Ashina; Itsuko Sato; Kandai Nozu
Journal:  J Clin Med       Date:  2022-08-31       Impact factor: 4.964

  3 in total

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