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  2. Myositis - Wikipedia

    en.wikipedia.org/wiki/Myositis

    In some instances, the origins of myositis remain idiopathic, without a discernible cause. Injury - A mild form of myositis can occur with hard exercise. [4] A more severe form of muscle injury, called rhabdomyolysis, is also associated with myositis. [4] This is a condition where an injury to the patient's muscles causes them to quickly break ...

  3. Dermatomyositis - Wikipedia

    en.wikipedia.org/wiki/Dermatomyositis

    Diagnosis is typically based on some combination of symptoms, blood tests, electromyography, and muscle biopsies. [3] Eighty percent of adults with adult-onset dermatomyositis have a myositis-specific antibody (MSA). [5] Sixty percent of children with juvenile dermatomyositis have a myositis-specific antibody (MSA). [6]

  4. Inflammatory myopathy - Wikipedia

    en.wikipedia.org/wiki/Inflammatory_myopathy

    overlapping symptoms (such as muscle weakness, pain, elevated CK); that delaying treatment for an inflammatory myopathy, in order to exclude potential non-inflammatory myopathies, may cause irreversible damage (although administering immunosuppressants and glucocorticosteroids to non-inflammatory myopathies may also cause damage);

  5. Polymyositis - Wikipedia

    en.wikipedia.org/wiki/Polymyositis

    Polymyositis and the associated inflammatory myopathies have an associated increased risk of cancer. [3] The features they found associated with an increased risk of cancer were older age, age greater than 45, male sex, difficulty swallowing, death of skin cells, cutaneous vasculitis, rapid onset of myositis (<4 weeks), elevated creatine kinase, higher erythrocyte sedimentation rate and higher ...

  6. Statin-associated autoimmune myopathy - Wikipedia

    en.wikipedia.org/wiki/Statin-associated...

    The exact cause is unclear. A combination of consistent findings on physical examination, the presence of anti HMG-CoA reductase antibodies in a person with myopathy, evidence of muscle breakdown, and muscle biopsy diagnose SAAM. [3] Treatment involves stopping the associated statin medication and taking medication to suppress the immune system.

  7. Inclusion body myositis - Wikipedia

    en.wikipedia.org/wiki/Inclusion_body_myositis

    Inclusion body myositis (IBM) (/ m aɪ oʊ ˈ s aɪ t ɪ s /) (sometimes called sporadic inclusion body myositis, sIBM) is the most common inflammatory muscle disease in older adults. [2] The disease is characterized by slowly progressive weakness and wasting of both proximal muscles (located on or close to the torso ) and distal muscles (close ...

  8. Myopathy - Wikipedia

    en.wikipedia.org/wiki/Myopathy

    (G71.0) Dystrophies (or muscular dystrophies) are a subgroup of myopathies characterized by muscle degeneration and regeneration. Clinically, muscular dystrophies are typically progressive, because the muscles' ability to regenerate is eventually lost, leading to progressive weakness, often leading to use of a wheelchair, and eventually death, usually related to respiratory weakness.

  9. Bornholm disease - Wikipedia

    en.wikipedia.org/wiki/Bornholm_disease

    Bornholm disease is a clinical diagnosis that uses the spasmodic pain, fever, and relapses to distinguish the illness from other potential causes of pain such as appendicitis or myocardial infarction. [5] Tachycardia and arrhythmias have been found with Bornholm disease by using an electrocardiogram (ECG). Murmurs, rubs, and pericardial ...