Journal of IMAB (Oct 2008)

KERATODERMA BLENORRHAGICUM IN A PATIENT WITH REITER SYNDROME

  • Valentina Dimitrova,
  • Valentin Valtchev,
  • Ivelina Yordanova,
  • Hristina Haidudova,
  • Dimitar Gospodinov,
  • Snejana Tisheva

DOI
https://doi.org/10.5272/jimab.14-1-2010.68
Journal volume & issue
Vol. 14, no. 1
pp. 68 – 71

Abstract

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Reiter syndrome is a systemic disorder, originally defined as a triad of arthritis, urethritis and conjunctivitis. This symptoms complex usually follows an episode of either urethritis or dysentery. Skin and mucosal involvement is observed in about 10% of the cases. We present a case of Reiter’s syndrome in a 55-year-old man who developed the typical skin lesions - kerathoderma blenorrhagicum. The disease started with a severe asymmetric oligoarthritis a month after the patient had urethritis. Two weeks after the onset of the arthritis red patches on the palms and plants appeared, which transformed quickly in harder and elevated plaques.

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