Myositis

Changed by Francis Deng, 7 Sep 2020

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MyositisMyopathy and myositis
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Myositis is the inflammation of muscle and is considered a generic non-specific term. Myopathy refers to a broad range of diseases of skeletal muscle that lead to dysfunction of muscle fibres, some. Myositis is the subset of which are cause myositismyopathy characterized by inflammation of muscle. There There is often significant overlap leading to the terms being used interchangeably.

Pathology

MyositisEtiology

There are numerous specific types of myositis, whichMyopathies and myositides can be generally categorised as follows1:

Myositis ossificans is considered a different entity.

Myopathy

Myopathies can be generally categorised as follows:

  • hereditary myopathiesmyopathy
  • inflammatory and infectious myositides: see above
  • endocrine myopathiesmyopathy
    • associated with adrenal, thyroid, parathyroid and pituitary dysfunction
  • drug-induceddenervation myopathy
    • such as corticosteroids
  • systemic conditions, such as sarcoidosisdue to peripheral neuropathy

Myositis ossificans is considered a different entity.

Radiographic features

MRMRI is the gold standard modality for noninvasive evaluation of myositis, which shows classic edema signal pattern (high T2WI and STIR signal) in affected muscles. Inflamed muscles demonstrate contrast enhancement.

If chronic, T1WI will show high muscle signal indicating fat replacement and atrophy.

  • -<p><strong>Myositis</strong> is the inflammation of muscle and is considered a generic non-specific term. <strong>Myopathy</strong> refers to a broad range of diseases of skeletal muscle that lead to dysfunction of muscle fibres, some of which are cause myositis. There is often significant overlap leading to the terms being used interchangeably.</p><h4>Pathology</h4><h5>Myositis</h5><p>There are numerous specific types of myositis, which can be categorised as follows:</p><ul>
  • +<p><strong>Myopathy</strong> refers to a broad range of diseases of skeletal muscle that lead to dysfunction of muscle fibres. <strong>Myositis</strong> is the subset of myopathy characterized by inflammation of muscle. There is often significant overlap leading to the terms being used interchangeably.</p><h4>Pathology</h4><h5>Etiology</h5><p>Myopathies and myositides can be generally categorised as follows <sup>1</sup>:</p><ul>
  • +<li><a href="/articles/anti-synthetase-syndrome-1">antisynthetase syndrome</a></li>
  • +<li><a href="/articles/immune-mediated-necrotizing-myopathy">immune-mediated necrotizing myopathy</a></li>
  • -<li><a title="eosinophilic myositis" href="/articles/eosinophilic-myositis">eosinophilic myositis</a></li>
  • +<li><a href="/articles/eosinophilic-myositis">eosinophilic myositis</a></li>
  • -<li>chronic <a title="Graft versus host disease" href="/articles/graft-versus-host-disease">graft versus host disease</a> <sup>2</sup>
  • +<li>chronic <a href="/articles/graft-versus-host-disease">graft versus host disease</a> <sup>2</sup>
  • -<a href="/articles/infectious-myositis">infectious myositis</a><ul>
  • -<li>bacterial myositis: may be complicated by pyomyositis</li>
  • -<li>viral myositis: may be complicated by <a title="Rhabdomyolysis" href="/articles/rhabdomyolysis">rhabdomyolysis</a>
  • +<a href="/articles/infectious-myositis">infectious myositis</a> <sup>3</sup><ul>
  • +<li>bacterial myositis (<a href="/articles/infectious-myositis">pyomyositis</a>)</li>
  • +<li>viral myositis<ul>
  • +<li>
  • +<a href="/articles/influenza">influenza</a> myositis</li>
  • +<li>coxsackievirus B virus-related pleurodynia (<a href="/articles/bornholm-disease-1">Bornholm disease</a>)</li>
  • +<li>virus-associated <a href="/articles/rhabdomyolysis">rhabdomyolysis</a>
  • +</li>
  • +</ul>
  • +</li>
  • +<li>parasitic myositis (a cause of eosinophilic myositis)<ul>
  • +<li><a href="/articles/cysticercosis">cysticercosis</a></li>
  • +<li><a href="/articles/trichinosis">trichinosis</a></li>
  • +</ul>
  • +<li>fungal myositis (rare)</li>
  • -<li>drug-related myositis<ul><li>statin-related myositis: can persist after discontinuation of the drug</li></ul>
  • +<li>drug-related myositis or myopathy<ul>
  • +<li>statin-related myositis: can persist after discontinuation of the drug</li>
  • +<li>steroid myopathy</li>
  • +</ul>
  • -</ul><p><a href="/articles/myositis-ossificans-1">Myositis ossificans</a> is considered a different entity.</p><h5>Myopathy</h5><p>Myopathies can be generally categorised as follows:</p><ul>
  • -<li>hereditary myopathies<ul>
  • +<li>hereditary myopathy<ul>
  • -<li>inflammatory and infectious myositides: see above</li>
  • -<li>endocrine myopathies<ul><li>associated with adrenal, thyroid, parathyroid and pituitary dysfunction</li></ul>
  • +<li>endocrine myopathy<ul><li>associated with adrenal, thyroid, parathyroid and pituitary dysfunction</li></ul>
  • -<li>drug-induced myopathy<ul><li>such as corticosteroids</li></ul>
  • -</li>
  • -<li>systemic conditions such as sarcoidosis</li>
  • -</ul><h4>Radiographic features</h4><p>MR is the gold standard modality, which shows classic edema signal pattern (high T2WI and STIR signal) in affected muscles. Inflamed muscles demonstrate contrast enhancement.</p><p>If chronic, T1WI will show high muscle signal indicating fat replacement and atrophy.</p>
  • +<li>
  • +<a href="/articles/denervation-changes-in-muscles">denervation myopathy</a>, such as due to peripheral neuropathy</li>
  • +</ul><p>​<a href="/articles/myositis-ossificans-1">Myositis ossificans</a> is considered a different entity.</p><h4>Radiographic features</h4><p>MRI is the gold standard modality for noninvasive evaluation of myositis, which shows classic edema signal pattern (high T2WI and STIR signal) in affected muscles. Inflamed muscles demonstrate contrast enhancement.</p><p>If chronic, T1WI will show high muscle signal indicating fat replacement and atrophy.</p>

References changed:

  • 3. Crum-Cianflone NF. Bacterial, fungal, parasitic, and viral myositis. (2008) Clinical microbiology reviews. 21 (3): 473-94. <a href="https://doi.org/10.1128/CMR.00001-08">doi:10.1128/CMR.00001-08</a> - <a href="https://www.ncbi.nlm.nih.gov/pubmed/18625683">Pubmed</a> <span class="ref_v4"></span>

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