Abstract
Dermatomyositis is an idiopathic inflammatory myopathy characterized by different skin and/or muscle involvement and possible visceral organ manifestation. Dermatomyositis is associated with an increased risk of malignancy; therapeutic options include systemic immunosuppression with high-dose corticosteroids and adjuvant immunosuppressants. In refractory patients, high-dose intravenous immunoglobulins and rituximab are useful. A mixed connective tissue disease is a multi-organ disease with symptoms of other systemic autoimmune diseases, mostly systemic scleroderma and systemic lupus erythematosus with muscle and joint involvement. The detection of anti-U1RNP IgG autoantibodies is a diagnostic clue. In the context of rheumatoid arthritis, polymorphic, inflammatory nodular, vasculitic, and ulcerative skin lesions may appear on the skin. The detection of serum IgG autoantibodies against the transcription factor ΔNp63α is pathognomonic for the diagnosis of chronic ulcerative stomatitis.
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Eming, R., Didona, D. (2021). Dermatomyositis and Other Autoimmune Disorders. In: Plewig, G., French, L., Ruzicka, T., Kaufmann, R., Hertl, M. (eds) Braun-Falco´s Dermatology. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-662-58713-3_55-1
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