Carnitne Palmitoyltransferase II Defciency, a Rare Cause of Rhabdomyolysis: A Case Report

Introduction: Muscle weakness and rhabdomyolysis have a wide range of differential diagnosis. In many situations, they are induced by seizure, trauma, drugs, and toxins. They could also be due to inflammatory or metabolic myopathies. Identifying the exact cause is crucial and sometimes challenging....

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Main Authors: Parisa Farshchi, Sahar Karimpour Reyhan, Mahsa Abbaszadeh, Shadi Shiva
Format: Article
Language:English
Published: Tehran University of Medical Sciences 2019-11-01
Series:Case Reports in Clinical Practice
Subjects:
Online Access:https://crcp.tums.ac.ir/index.php/crcp/article/view/282
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spelling doaj-e7ec6f0082284f04a754a734160f9d312020-11-25T04:01:47ZengTehran University of Medical SciencesCase Reports in Clinical Practice2538-26832538-26912019-11-014310.18502/crcp.v4i3.1715Carnitne Palmitoyltransferase II Defciency, a Rare Cause of Rhabdomyolysis: A Case ReportParisa Farshchi0Sahar Karimpour Reyhan1Mahsa Abbaszadeh2Shadi Shiva3Department of Internal Medicine, Imam Khomeini Hospital Complex, Tehran University of Medical Sciences, Tehran, IranDepartment of Internal Medicine, Imam Khomeini Hospital Complex, Tehran University of Medical Sciences, Tehran, IranDepartment of Internal Medicine, Imam Khomeini Hospital Complex, Tehran University of Medical Sciences, Tehran, IranPediatric Neurology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran. Introduction: Muscle weakness and rhabdomyolysis have a wide range of differential diagnosis. In many situations, they are induced by seizure, trauma, drugs, and toxins. They could also be due to inflammatory or metabolic myopathies. Identifying the exact cause is crucial and sometimes challenging. Case Presentation: A 23-year-old man was admitted to our hospital with muscle weakness, fatigue, dyspnea, and dark urine, all preceded by flu-like symptoms, myalgia, and fever. Due to reduced muscle strength, dark urine, elevated serum creatine kinase, and serum creatinine, he was diagnosed with rhabdomyolysis and acute kidney injury. Muscle biopsy was performed three years before for the patient, due to a history of similar episodes and exercise intolerance. Because of recurrent episodes of muscle weakness and rhabdomyolysis along with the negative muscle biopsy for inflammatory myopathies, we suspected metabolic myopathy as a cause. Therefore, metabolic screening was performed for the patient, and he was diagnosed with metabolic myopathy known as Carnitine Palmitoyltransferase II (CPT II) deficiency. Conclusion: In patients with recurrent rhabdomyolysis, we should consider inherited myopathies, especially carnitine palmitoyltransferase II deficiency and glycogen storage disease type V (McArdle disease) as likely causes. CPT II deficiency is regarded as a preventable cause of recurrent rhabdomyolysis. Therefore, by early diagnosis of this disorder we could prevent recurrent episodes of rhabdomyolysis and ultimately avoid life threatening complications like acute kidney injury. https://crcp.tums.ac.ir/index.php/crcp/article/view/282Rhabdomyolysis;Acute kidney injury;Carnitne palmitoyltransferase II defciency;Metabolic myopathy
collection DOAJ
language English
format Article
sources DOAJ
author Parisa Farshchi
Sahar Karimpour Reyhan
Mahsa Abbaszadeh
Shadi Shiva
spellingShingle Parisa Farshchi
Sahar Karimpour Reyhan
Mahsa Abbaszadeh
Shadi Shiva
Carnitne Palmitoyltransferase II Defciency, a Rare Cause of Rhabdomyolysis: A Case Report
Case Reports in Clinical Practice
Rhabdomyolysis;
Acute kidney injury;
Carnitne palmitoyltransferase II defciency;
Metabolic myopathy
author_facet Parisa Farshchi
Sahar Karimpour Reyhan
Mahsa Abbaszadeh
Shadi Shiva
author_sort Parisa Farshchi
title Carnitne Palmitoyltransferase II Defciency, a Rare Cause of Rhabdomyolysis: A Case Report
title_short Carnitne Palmitoyltransferase II Defciency, a Rare Cause of Rhabdomyolysis: A Case Report
title_full Carnitne Palmitoyltransferase II Defciency, a Rare Cause of Rhabdomyolysis: A Case Report
title_fullStr Carnitne Palmitoyltransferase II Defciency, a Rare Cause of Rhabdomyolysis: A Case Report
title_full_unstemmed Carnitne Palmitoyltransferase II Defciency, a Rare Cause of Rhabdomyolysis: A Case Report
title_sort carnitne palmitoyltransferase ii defciency, a rare cause of rhabdomyolysis: a case report
publisher Tehran University of Medical Sciences
series Case Reports in Clinical Practice
issn 2538-2683
2538-2691
publishDate 2019-11-01
description Introduction: Muscle weakness and rhabdomyolysis have a wide range of differential diagnosis. In many situations, they are induced by seizure, trauma, drugs, and toxins. They could also be due to inflammatory or metabolic myopathies. Identifying the exact cause is crucial and sometimes challenging. Case Presentation: A 23-year-old man was admitted to our hospital with muscle weakness, fatigue, dyspnea, and dark urine, all preceded by flu-like symptoms, myalgia, and fever. Due to reduced muscle strength, dark urine, elevated serum creatine kinase, and serum creatinine, he was diagnosed with rhabdomyolysis and acute kidney injury. Muscle biopsy was performed three years before for the patient, due to a history of similar episodes and exercise intolerance. Because of recurrent episodes of muscle weakness and rhabdomyolysis along with the negative muscle biopsy for inflammatory myopathies, we suspected metabolic myopathy as a cause. Therefore, metabolic screening was performed for the patient, and he was diagnosed with metabolic myopathy known as Carnitine Palmitoyltransferase II (CPT II) deficiency. Conclusion: In patients with recurrent rhabdomyolysis, we should consider inherited myopathies, especially carnitine palmitoyltransferase II deficiency and glycogen storage disease type V (McArdle disease) as likely causes. CPT II deficiency is regarded as a preventable cause of recurrent rhabdomyolysis. Therefore, by early diagnosis of this disorder we could prevent recurrent episodes of rhabdomyolysis and ultimately avoid life threatening complications like acute kidney injury.
topic Rhabdomyolysis;
Acute kidney injury;
Carnitne palmitoyltransferase II defciency;
Metabolic myopathy
url https://crcp.tums.ac.ir/index.php/crcp/article/view/282
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AT mahsaabbaszadeh carnitnepalmitoyltransferaseiidefciencyararecauseofrhabdomyolysisacasereport
AT shadishiva carnitnepalmitoyltransferaseiidefciencyararecauseofrhabdomyolysisacasereport
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