Title of article
Severe lactic acidosis secondary to minocycline in a teenager with infectious mononucleosis and mitochondrial myopathy
Author/Authors
Richard M. Zoraster، نويسنده , , Richard A. Rison، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 2008
Pages
4
From page
627
To page
630
Abstract
Mitochondrial myopathies are heterogeneous disorders with diverse presentations including laboratory findings of lactic acidosis. Often times they are diagnosed in childhood or the early teenage years following an infectious illness. Minocycline is a common antibiotic used for the treatment of acne. It has been reported to alter mitochondrial respiratory chain complexes. We report an interesting case of a teenager in which mitochondrial myopathy with severe lactic acidosis presented following a bout of infectious mononucleosis and minocycline use. It is hypothesized that oxidative stress from the infectious illness plus the minocycline use triggered the patientʹs presentation. The clinical manifestations and genetics of mitochondrial myopathies and treatment are discussed along with the management of lactic acidosis.
Keywords
Infectious mononucleosis , Lactic acidosis , Mitochondrial myopathy , Minocycline , G8363A mutation , Ribosome inhibitor , Respiratory chaincomplexes
Journal title
Clinical Neurology and Neurosurgery
Serial Year
2008
Journal title
Clinical Neurology and Neurosurgery
Record number
464666
Link To Document