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Rhabdomyolysis with different etiologies in childhood

AIM: To investigate different etiologies and management of the rhabdomyolysis in children. METHODS: Eight pediatric rhabdomyolysis cases who applied to the Dokuz Eylul University Faculty of Medicine Department of Pediatric Nephrology with different etiologies between January 2004 and January 2012 we...

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Autores principales: Alaygut, Demet, Torun Bayram, Meral, Kasap, Belde, Soylu, Alper, Türkmen, Mehmet, Kavukcu, Salih
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5691034/
https://www.ncbi.nlm.nih.gov/pubmed/29184760
http://dx.doi.org/10.5409/wjcp.v6.i4.161
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author Alaygut, Demet
Torun Bayram, Meral
Kasap, Belde
Soylu, Alper
Türkmen, Mehmet
Kavukcu, Salih
author_facet Alaygut, Demet
Torun Bayram, Meral
Kasap, Belde
Soylu, Alper
Türkmen, Mehmet
Kavukcu, Salih
author_sort Alaygut, Demet
collection PubMed
description AIM: To investigate different etiologies and management of the rhabdomyolysis in children. METHODS: Eight pediatric rhabdomyolysis cases who applied to the Dokuz Eylul University Faculty of Medicine Department of Pediatric Nephrology with different etiologies between January 2004 and January 2012 were evaluated in terms of age, gender, admission symptoms, physical examination findings, factors provoking rhabdomyolysis, number of rhabdomyolysis attacks, laboratory results, family history and the final diagnosis received after the treatment. RESULTS: Average diagnosis ages of eight cases were 129 (24-192) ± 75.5 mo and five of them were girls. All of them had applied with the complaint of muscle pain, calf pain, and dark color urination. Infection (pneumonia) and excessive physical activity were the most important provocative factors and excessive licorice consumption was observed in one case. In 5 cases, acute kidney injury was determined and two cases needed hemodialysis. As a result of the further examinations; the cases had received diagnoses of rhabdomyolysis associated with mycoplasma pneumoniae, sepsis associated rhabdomyolysis, licorice-induced hypokalemic rhabdomyolysis, carnitine palmitoyltransferase II deficiency, very long-chain acyl-CoA dehydrogenase deficiency, congenital muscular dystrophy and idiopathic paroxysmal rhabdomyolysis (Meyer-Betz syndrome). CONCLUSION: It is important to distinguish the sporadic and recurrent rhabdomyolysis cases from each other. Recurrent rhabdomyolysis cases should follow up more regardful and attentive.
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spelling pubmed-56910342017-11-28 Rhabdomyolysis with different etiologies in childhood Alaygut, Demet Torun Bayram, Meral Kasap, Belde Soylu, Alper Türkmen, Mehmet Kavukcu, Salih World J Clin Pediatr Retrospective Study AIM: To investigate different etiologies and management of the rhabdomyolysis in children. METHODS: Eight pediatric rhabdomyolysis cases who applied to the Dokuz Eylul University Faculty of Medicine Department of Pediatric Nephrology with different etiologies between January 2004 and January 2012 were evaluated in terms of age, gender, admission symptoms, physical examination findings, factors provoking rhabdomyolysis, number of rhabdomyolysis attacks, laboratory results, family history and the final diagnosis received after the treatment. RESULTS: Average diagnosis ages of eight cases were 129 (24-192) ± 75.5 mo and five of them were girls. All of them had applied with the complaint of muscle pain, calf pain, and dark color urination. Infection (pneumonia) and excessive physical activity were the most important provocative factors and excessive licorice consumption was observed in one case. In 5 cases, acute kidney injury was determined and two cases needed hemodialysis. As a result of the further examinations; the cases had received diagnoses of rhabdomyolysis associated with mycoplasma pneumoniae, sepsis associated rhabdomyolysis, licorice-induced hypokalemic rhabdomyolysis, carnitine palmitoyltransferase II deficiency, very long-chain acyl-CoA dehydrogenase deficiency, congenital muscular dystrophy and idiopathic paroxysmal rhabdomyolysis (Meyer-Betz syndrome). CONCLUSION: It is important to distinguish the sporadic and recurrent rhabdomyolysis cases from each other. Recurrent rhabdomyolysis cases should follow up more regardful and attentive. Baishideng Publishing Group Inc 2017-11-08 /pmc/articles/PMC5691034/ /pubmed/29184760 http://dx.doi.org/10.5409/wjcp.v6.i4.161 Text en ©The Author(s) 2017. Published by Baishideng Publishing Group Inc. All rights reserved. http://creativecommons.org/licenses/by-nc/4.0/ Open-Access: This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/
spellingShingle Retrospective Study
Alaygut, Demet
Torun Bayram, Meral
Kasap, Belde
Soylu, Alper
Türkmen, Mehmet
Kavukcu, Salih
Rhabdomyolysis with different etiologies in childhood
title Rhabdomyolysis with different etiologies in childhood
title_full Rhabdomyolysis with different etiologies in childhood
title_fullStr Rhabdomyolysis with different etiologies in childhood
title_full_unstemmed Rhabdomyolysis with different etiologies in childhood
title_short Rhabdomyolysis with different etiologies in childhood
title_sort rhabdomyolysis with different etiologies in childhood
topic Retrospective Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5691034/
https://www.ncbi.nlm.nih.gov/pubmed/29184760
http://dx.doi.org/10.5409/wjcp.v6.i4.161
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