Behcet's disease is a complex multisystem disease diagnosed by means of cli
nical criteria. Clinical features include oral and genital aphthae, pustula
r vasculitic cutaneous lesions, and ocular, gastrointestinal, and vascular
manifestations. We believe that complex aphthosis, characterized by oral or
oral and genital ulcers, may be a forme fruste of Behcet's disease. Althou
gh the pathogenesis of both Behcet's disease and complex aphthosis remain u
nknown, immune factors, infectious agents, and effector mechanisms are impl
icated. Treatment is based on the severity of systemic involvement and incl
udes topical therapies as well as colchicine, dapsone, thalidomide, and imm
unosuppressive agents.