Abstract
Relapsing polychondritis (RP) is a systemic disease of unknown etiology, associated with the formation of antibodies to type II collagen, the type of collagen predominating in the cartilage. This results in inflammation of the cartilage of the ears, nose, tracheobronchial tree, and joints (Foidart et al., New Engl J Med., 1978;299:1203–7). Involvement of the inner ear and heart may be explained by evidence suggesting that type II collagen exists in those tissues (Rahkonen et al., Histochem Cell Biol. 2003;120:103–10; Dreiling et al., Hear Res. 2002;166:181–91). Murine models suggest that tissue-specific antibody and complement activation are both necessary for expression of the disease (Hansson et al. Am J Pathol. 2004;164:959–966).
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Somach, S.C. (2016). Relapsing Polychondritis. In: Crowe, D., Morgan, M., Somach, S., Trapp, K. (eds) Deadly Dermatologic Diseases. Springer, Cham. https://doi.org/10.1007/978-3-319-31566-9_39
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DOI: https://doi.org/10.1007/978-3-319-31566-9_39
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