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Rhabdomyolysis with different etiologies in childhood
Demet Alaygut1, Meral Torun Bayram2, Belde Kasap2
1Department of Pediatric Nephrology, Dokuz Eylul University Faculty of Medicine, 35340 İnciralti İzmir, Turkey. demet.alaygut@deu.edu.tr.
Insights
This study reviewed eight pediatric rhabdomyolysis cases, identifying infection, physical activity, and licorice as key triggers. Differentiating recurrent from sporadic cases is crucial for appropriate pediatric rhabdomyolysis management.
Area of Science:
- Pediatric Nephrology
- Neurology
- Genetics
Background:
- Rhabdomyolysis in children presents with diverse etiologies and clinical manifestations.
- Prompt diagnosis and management are essential to prevent complications like acute kidney injury.
Purpose of the Study:
- To investigate the various causes and treatment strategies for rhabdomyolysis in pediatric patients.
- To analyze clinical data from pediatric rhabdomyolysis cases to identify common triggers and outcomes.
Main Methods:
- Retrospective evaluation of eight pediatric rhabdomyolysis cases.
- Analysis included patient demographics, symptoms, physical findings, provocative factors, laboratory results, and diagnoses.
Main Results:
- Infection (pneumonia) and excessive physical activity were primary triggers; excessive licorice consumption was noted in one case.
- Five patients developed acute kidney injury, with two requiring hemodialysis.
- Diagnoses included Mycoplasma pneumoniae, sepsis, licorice-induced hypokalemia, genetic disorders (CPT II, VLCAD, congenital muscular dystrophy), and idiopathic paroxysmal rhabdomyolysis.
Conclusions:
- Distinguishing between sporadic and recurrent rhabdomyolysis is vital.
- Recurrent pediatric rhabdomyolysis necessitates closer monitoring and attentive management.
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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