Literature DB >> 17110865

Hyponatremic dehydration as a presentation of cystic fibrosis.

Yolanda Ballestero1, María Isabel Hernandez, Pablo Rojo, Javier Manzanares, Verónica Nebreda, Helena Carbajosa, Elena Infante, María Baro.   

Abstract

BACKGROUND: The purpose of this study is to present a case report of a child with hyponatremic dehydration diagnosed after CF and to review the cases of 13 patients with CF who had the same initial presentation in our hospital.
METHODS: This report reviewed the clinical records of children diagnosed with CF to ascertain the prevalence of metabolic alkalosis with electrolyte depletion as the presentation of CF. It also used sweat tests to diagnose a child with CF.
RESULTS: The laboratory tests of a 12-month-old girl presented 3 times to the ;pediatric emergency department with vomiting and weight loss showed hyponatremia, hypochloremia, and metabolic alkalosis. The patient was subsequently diagnosed with CF by means of 2 positive sweat tests. Meanwhile, the review of the clinical records of all children diagnosed with CF from 1985 to 2004 (N = 77) showed that the prevalence of metabolic alkalosis with electrolyte depletion as the presentation of CF was 16.8%. The age of the infants ranged from 3 to 14 months. All episodes took place during summer.
CONCLUSIONS: There are not many causes of metabolic alkalosis with hyponatremic dehydration, and one of them is CF. This report emphasizes sodium depletion as a common sign of CF presentation. This is most important in countries where the neonatal screening test for CF is not available because the disease may be asymptomatic or oligosymptomatic for several months or even years. Cystic fibrosis should be considered in differential diagnosis of any child presenting with unexplained hyponatremic dehydration.

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Year:  2006        PMID: 17110865     DOI: 10.1097/01.pec.0000245170.31343.bb

Source DB:  PubMed          Journal:  Pediatr Emerg Care        ISSN: 0749-5161            Impact factor:   1.454


  16 in total

1.  Autosomal recessive hyponatremia due to isolated salt wasting in sweat associated with a mutation in the active site of Carbonic Anhydrase 12.

Authors:  Emad Muhammad; Neta Leventhal; Galit Parvari; Aaron Hanukoglu; Israel Hanukoglu; Vered Chalifa-Caspi; Yael Feinstein; Jenny Weinbrand; Harel Jacoby; Esther Manor; Tal Nagar; John C Beck; Val C Sheffield; Eli Hershkovitz; Ruti Parvari
Journal:  Hum Genet       Date:  2010-12-24       Impact factor: 4.132

2.  Acute renal failure in people with cystic fibrosis.

Authors:  Kevin W Southern
Journal:  Thorax       Date:  2007-06       Impact factor: 9.139

3.  Renovascular hypertension: a case with atypical neurological signs.

Authors:  Mónica Jerónimo; Teresa Dionísio; Clara Gomes; José Farela Neves
Journal:  BMJ Case Rep       Date:  2015-09-08

4.  Renal function in pediatric cystic fibrosis patients in the first decade of life.

Authors:  Chanel Prestidge; Mark A Chilvers; A George F Davidson; Eva Cho; Vanessa McMahon; Colin T White
Journal:  Pediatr Nephrol       Date:  2010-12-29       Impact factor: 3.714

5.  The fractional excretion of sodium in patients with cystic fibrosis treated with oral sodium chloride.

Authors:  Majid Keivanfar; Sosan Daris; Mohsen Reisi; Mehryar Mehrkesh
Journal:  Am J Clin Exp Urol       Date:  2020-12-15

Review 6.  Electrolyte abnormalities in cystic fibrosis: systematic review of the literature.

Authors:  Elisabetta Scurati-Manzoni; Emilio F Fossali; Carlo Agostoni; Enrica Riva; Giacomo D Simonetti; Maura Zanolari-Calderari; Mario G Bianchetti; Sebastiano A G Lava
Journal:  Pediatr Nephrol       Date:  2013-12-11       Impact factor: 3.714

7.  Cystic fibrosis, aminoglycoside treatment and acute renal failure: the not so gentle micin.

Authors:  Detlef Bockenhauer; Martin J Hug; Robert Kleta
Journal:  Pediatr Nephrol       Date:  2008-11-13       Impact factor: 3.714

8.  Adrenal crisis caused by inhaled fluticasone in an adolescent with cystic fibrosis and advanced hepatopathy: a case report.

Authors:  C Denne; A E Vogl-Voswinckel; A Gruebl; S Burdach
Journal:  Case Rep Pulmonol       Date:  2012-09-29

9.  Metabolic alkalosis in adults with stable cystic fibrosis.

Authors:  Fahad Al-Ghimlas; Marie E Faughnan; Elizabeth Tullis
Journal:  Open Respir Med J       Date:  2012-07-25

10.  Nanoduct sweat conductivity measurements in 2664 patients: relationship to age, arterial blood gas, serum electrolyte profiles and clinical diagnosis.

Authors:  Rabia Gonul Sezer; Gokhan Aydemir; Abdullah Baris Akcan; Cem Paketci; Abdulbaki Karaoglu; Secil Aydinoz; Abdulkadir Bozaykut
Journal:  J Clin Med Res       Date:  2013-01-11
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