Abstract
Muscle is particularly susceptible to toxic effects of drugs or toxins due to its high metabolic activity and potential sites for disruption of energy-producing pathways.
Toxic and drug-induced myopathies describe a wide spectrum of clinical presentations caused by an even wider array of therapeutic agents, recreational and illicit drugs, or environmental or occupational toxins. The mechanisms of toxic myopathy are again almost as varied as the list of causative substances.
Failure to recognize the often iatrogenic nature of these myopathies with continuation of drug or toxin exposure may unnecessarily prolong patient morbidity and can lead to potentially fatal outcomes.
Diagnosis of toxic myopathy rests primarily on patient drug or environmental exposure history, laboratory studies (esp. serum creatine kinase), and electrophysiological studies. Clinical neuroradiology, relying primarily on MRI, will not reveal findings or patterns specific to any single toxic myopathy, but it can play a crucial role in establishing disease pattern for biopsy, elucidating complications (e.g., muscle necrosis), and disease monitoring.
Illustration of neuroradiological findings of all toxic agents is not practicable; therefore, the following chapter will focus on three major agents of toxic myopathy: statin-, glucocorticoid-, and alcohol-induced myopathy.
This publication is endorsed by: European Society of Neuroradiology (www.esnr.org).
Abbreviations
- AIM:
-
Alcohol-induced myopathy
- CK:
-
Creatine kinase
- GIM:
-
Glucocorticoid-induced myopathy
- SIM:
-
Statin-induced myopathy
- STIR:
-
Short tau inversion recovery
- TDIM:
-
Toxic and drug-induced myopathy
- ULN:
-
Upper limit of normal
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Suggestions for Further Reading
Dalakas MC. Toxic and drug-induced myopathies. J Neurol Neurosurg Psychiatry. 2009;80:832–8.
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Peters, S.A., Kley, R.A. (2019). Toxic and Drug-Induced Myopathies. In: Barkhof, F., Jager, R., Thurnher, M., Rovira Cañellas, A. (eds) Clinical Neuroradiology. Springer, Cham. https://doi.org/10.1007/978-3-319-61423-6_4-1
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DOI: https://doi.org/10.1007/978-3-319-61423-6_4-1
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