Abstract
Reiter’s syndrome is a postinfectious syndrome characterized by arthritis, conjunctivitis, and urethritis or cervicitis. In 1916 Hans Reiter described the case of a Prussian cavalry officer serving in the Balkans who developed arthritis, urethritis, and conjunctivitis 8 days following a diarrheal illness. Reiter attributed the condition to a spirochetal or syphilitic type of infection, although the patient denied venereal exposure1. Reiter was not the first to describe these symptoms. Among others the disease process had already been described by Sir Benjamin Brodie in 18182. A more extensive survey of the historical literature is cited by Paronen3, Calin4, and Keat5. The eponym, Reiter’s syndrome, is now attached to reactive arthritis occurring after such diseases as Shigella flexneri dysentery3,6–13, Salmonella typhimurium 7,13–21, Yersinia enterocolitica 13,22–30, Campylobader jejuni enterocolitis31-36, and Chlamydia trachomatis urogenital infections37-46.
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References
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Kean, W.F., MacPherson, D.W. (1991). Reiter’s syndrome. In: Bellamy, N. (eds) Prognosis in the Rheumatic Diseases. Springer, Dordrecht. https://doi.org/10.1007/978-94-011-3896-3_8
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DOI: https://doi.org/10.1007/978-94-011-3896-3_8
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