2014
DOI: 10.1016/j.ncl.2014.04.009
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Toxic Myopathies

Abstract: Muscle tissue is highly sensitive to many substances. Early recognition of toxic myopathies is important, as they potentially are reversible on removal of the offending drug or toxin, with greater likelihood of complete resolution the sooner this is achieved. Clinical features range from mild muscle pain and cramps to severe weakness with rhabdomyolysis, renal failure, and even death. The pathogenic bases can be multifactorial. This article reviews some of the common toxic myopathies and their clinical present… Show more

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Cited by 49 publications
(76 citation statements)
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References 119 publications
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“…We recruited 202 HIV-infected children (median age 11 years [IQR [8][9][10][11][12][13]; 48.8% female) and 285 uninfected children (median age 10 years [IQR [8][9][10][11][12][13]; 48.8% female). There was no significant difference in age or sex…”
Section: Baseline Characteristics Of Participantsmentioning
confidence: 99%
“…We recruited 202 HIV-infected children (median age 11 years [IQR [8][9][10][11][12][13]; 48.8% female) and 285 uninfected children (median age 10 years [IQR [8][9][10][11][12][13]; 48.8% female). There was no significant difference in age or sex…”
Section: Baseline Characteristics Of Participantsmentioning
confidence: 99%
“…The muscle adverse events in patients with toxic SaMAEs stabilise and show marked improvement within 2-3 months following statin cessation. 18 Until recently, SaMAEs referred to the nonautoimmune form. 26 Autoimmune inflammatory myositis and/or necrotising myopathy, on the other hand, starts or persists even after drug discontinuation.…”
Section: Classificationmentioning
confidence: 99%
“…31 This pathology may occur without CK elevations as the muscle fibre damage is largely restricted to the intracellular space while the 32 In cases of toxic necrotising myopathy, muscle fibre necrosis with prominent phagocytosis and small basophilic regenerating fibres have been observed in patients with elevated serum CK levels and weakness or myalgia; these patients did not have detectable HMGCR antibodies. 18 In anti-HMGCR clinical syndrome, autoimmune inflammatory myositis and/or necrotising myopathy is observed. 17 Necrotising myopathy is a characteristic pathological pattern consisting of scattered muscle fibre necrosis and regeneration, macrophage infiltrates, a few endomysial inflammatory cells (including cluster of differentiation [CD] 4+ and CD8+ T cells and plasmacytoid dendritic cells) and sarcolemmal complement deposition on the surface of non-necrotic muscle fibres.…”
Section: Muscle Biopsy Findingsmentioning
confidence: 99%
“…These myopathies can be related to autoimmune mechanisms by the presence of specific autoantibodies such as anti-SRP and anti-HMGCR, or may be associated with specific connective tissue disorders [4]. Others are secondary to toxic agents [5], viral infections or reveal a paraneoplastic manifestation [2].…”
mentioning
confidence: 99%