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  2. Scleroderma - Wikipedia

    en.wikipedia.org/wiki/Scleroderma

    Mixed connective tissue disease, systemic lupus erythematosus, polymyositis, dermatomyositis [1] Treatment: Supportive care [1] Medication: Corticosteroids, methotrexate, non-steroidal anti-inflammatory drugs (NSAIDs) [2] Prognosis: Localized: Normal life expectancy [7] Systemic: Decreased life expectancy [3] Frequency: 3 per 100,000 per year ...

  3. Dermatomyositis - Wikipedia

    en.wikipedia.org/wiki/Dermatomyositis

    Dermatomyositis (DM) is a long-term inflammatory autoimmune disorder which affects the skin and the muscles. Its symptoms are generally a skin rash and worsening ...

  4. Scleromyositis - Wikipedia

    en.wikipedia.org/wiki/Scleromyositis

    Scleromyositis, is an autoimmune disease (a disease in which the immune system attacks the body). People with scleromyositis have symptoms of both systemic scleroderma and either polymyositis or dermatomyositis, and is therefore considered an overlap syndrome.

  5. Mixed connective tissue disease - Wikipedia

    en.wikipedia.org/wiki/Mixed_connective_tissue...

    In fact, some people may be completely asymptomatic. Myositis can be severe and difficult to differentiate from conventional dermatomyositis. [10] Myalgia is a prevalent complaint among patients with MCTD. [33]

  6. Inflammatory myopathy - Wikipedia

    en.wikipedia.org/wiki/Inflammatory_myopathy

    Around 3.2 children per million per year are diagnosed with DM (termed juvenile dermatomyositis), with an average age of onset of seven years. Diagnosis of adult DM commonly occurs between 30 and 50 years of age. PM is an adult disease, usually emerging after the age of twenty.

  7. 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 ...

  8. Juvenile dermatomyositis - Wikipedia

    en.wikipedia.org/wiki/Juvenile_dermatomyositis

    Juvenile dermatomyositis (JDM) is an idiopathic inflammatory myopathy (IMM) of presumed autoimmune dysfunction resulting in muscle weakness among other complications. It manifests itself in children; it is the pediatric counterpart of dermatomyositis .

  9. Antisynthetase syndrome - Wikipedia

    en.wikipedia.org/wiki/Antisynthetase_syndrome

    Dermatomyositis-like rashes are seen in 32–44% of those with antisynthetase syndrome. This includes heliotropic rash, Gottron papules, and lesions of the psoriasiform type that span the hand's dorsum and resemble the morphology of mechanics hands. [26]