Behcet disease: New aspects

Bulur I., Onder M.

CLINICS IN DERMATOLOGY, cilt.35, sa.5, ss.421-434, 2017 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 35 Sayı: 5
  • Basım Tarihi: 2017
  • Doi Numarası: 10.1016/j.clindermato1.2017.06.004
  • Dergi Adı: CLINICS IN DERMATOLOGY
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.421-434
  • Eskişehir Osmangazi Üniversitesi Adresli: Evet

Özet

Behcet disease is currently considered an "autoinfiammatory disease" triggered by infection and environmental factors in genetically predisposed individuals. Although the disease is characterized by recurrent oral and genital aphthous ulcers and ocular involvement, it can affect multiple organ systems. Complex aphthosis is characterized by recurrent oral and/or genital aphthous ulcers. It is important to evaluate the patient with complex aphthosis for Behcet disease and related systemic disorders. We discuss the etiopathogenesis, clinical features, diagnostic criteria, and treatment approaches for complex aphthosis and Behcet disease in light of the current literature. (C) 2017 Elsevier Inc. All rights reserved.