Synonyms
Definition
Was named in 1937 after the Turkish dermatologist Hulusi Behçet, who first described the triple-symptom complex of recurrent oral aphthous ulcers, genital ulcers, and uveitis. This complex, multisystemic disease includes involvement of the mucocutaneous, ocular, cardiovascular, renal, gastrointestinal, pulmonary, urologic, and central nervous systems and the joints, blood vessels, and lungs. It is characterized by oral aphthae and by at least two of the following: (i) genital aphthae, (ii) synovitis, (iii) posterior uveitis, (iv) cutaneous pustular vasculitis, (v) meningoencephalitis, (vi) recurrent genital ulcers, and (vii) uveitis in the absence of inflammatory bowel disease or collagen vascular disease. The cause of BD is not known; however, immunogenetics, immune regulation, vascular abnormalities, or bacterial and viral infection may have a role in its development.
This is a preview of subscription content, log in via an institution.
Author information
Authors and Affiliations
Corresponding author
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 2015 Springer-Verlag Berlin Heidelberg
About this entry
Cite this entry
Schwab, M. (2015). Behcet Disease. In: Schwab, M. (eds) Encyclopedia of Cancer. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-27841-9_578-3
Download citation
DOI: https://doi.org/10.1007/978-3-642-27841-9_578-3
Received:
Accepted:
Published:
Publisher Name: Springer, Berlin, Heidelberg
Online ISBN: 978-3-642-27841-9
eBook Packages: Springer Reference Biomedicine and Life SciencesReference Module Biomedical and Life Sciences