Literature DB >> 21771927

Mitochondrial myopathy presenting as rhabdomyolysis.

David C Patchett1, Michael L Grover.   

Abstract

A 37-year-old white woman presented with acute bilateral hamstring pain after hiking. She had a creatine kinase level of 11,144 U/L. Rhabdomyolysis was diagnosed and the patient was admitted for intravenous fluid hydration. The patient continued to have exercise-induced myalgias and elevations in her creatine kinase level. Rheumatologic causes were ruled out and results from electromyogram testing were nondiagnostic. A muscle biopsy revealed a mitochondrial myopathy. The 22 mitochondrial DNA and transfer RNA genes were sequenced. An A-to-G transition was found at nucleotide position 4281 in the transfer RNA isoleucine gene. The patient was placed on a regimen of riboflavin, vitamin C, and coenzyme Q10, which provided mild relief. The patient returned to the emergency department 2 more times after vigorous exercise, with creatine kinase levels as high as 2800 U/L. At last follow-up, the patient was using a fentanyl citrate transdermal patch, which enabled her to perform moderate exercise without pain.

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Year:  2011        PMID: 21771927

Source DB:  PubMed          Journal:  J Am Osteopath Assoc        ISSN: 0098-6151


  2 in total

1.  Genetic polymorphisms associated with exertional rhabdomyolysis.

Authors:  Patricia A Deuster; Carmen L Contreras-Sesvold; Francis G O'Connor; William W Campbell; Kimbra Kenney; John F Capacchione; Mark E Landau; Sheila M Muldoon; Elisabeth J Rushing; Yuval Heled
Journal:  Eur J Appl Physiol       Date:  2013-03-31       Impact factor: 3.078

2.  Complex-I defect with minimal manifestations.

Authors:  Josef Finsterer; Madleine Melichart; Adelheid Wöhrer
Journal:  Arch Med Sci       Date:  2014-02-23       Impact factor: 3.318

  2 in total

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