Behçet Disease

Sağ E. , Bilginer Y. , Özen S.

Periodic and Non-Periodic Fevers, Rolando Cimaz, Editör, Springer, London/Berlin , Milan, ss.161-176, 2020

  • Yayın Türü: Kitapta Bölüm / Mesleki Kitap
  • Basım Tarihi: 2020
  • Yayınevi: Springer, London/Berlin 
  • Basıldığı Şehir: Milan
  • Sayfa Sayıları: ss.161-176
  • Editörler: Rolando Cimaz, Editör


Behçet disease (BD) is a vasculitis that can affect arteries or veins of any size; thus, it was recently reclassified as a variable vessel vasculitis. BD is characterized by recurrent oral and/or genital ulcers accompanied by ocular, cutaneous, articular, gastrointestinal, and/or central nervous system inflammatory lesions [1]. Hulusi Behçet, a Turkish dermatologist, had described three major signs (oral aphthae, genital ulcerations, and uveitis) of BD in 1937 and defined it as a “triple symptom complex” [2]. There are also reports about BD description in the fifth century BC in the “Third Book of Endemic Diseases [3].”