Sep 15, · Behcet’s disease is a rare autoimmune disease. It causes damage to your blood vessels that can lead to sores in the mouth, rashes, and other symptoms. The severity of the disease varies from person Author: James Roland. Behçet's syndrome is a rare multisystem inflammatory disorder characterized by ulcers affecting the mouth and genitals, various skin lesions, and abnormalities affecting the eyes. Symptoms include mucous membrane lesions of the mouth (canker sores) and genitals (ulcers) that tend to disappear and recur spontaneously.
Skin lesions occurred in 64% of Behcet's patients from the United States and are often essential to meet diagnostic disease criteria. The ISG Criteria (Table 1) recognize erythema nodosum, pseudofolliculitis, papulopustular lesions, or acneiform nodules for the diagnosis. Histopathologic findings in lesions of erythema nodosum are those of a. pyoderma gangrenosum-like lesions, Sweet’s syndrome-like lesions, cutaneous vasculitis lesions which may present as palpable purpura, bullous or necrotizing lesions, facial and acral vesicopustules, extragenital ulcers and superficial thrombophlebitis. Skin involvement is a major feature of BD occurring in % of patients. In a recent.
Cutaneous manifestations of Behcet's Disease generally occur in % of patients. Erythema nodosum, an inflammation occurring in the fatty layer of the subcutaneous tissue, causes red tender nodules to form under the skin. These nodules frequently ulcerate, unlike the erythema nodosum lesions which occur with other diseases. Behçet disease (or syndrome) is a rare disease characterised by painful mouth ulcers, genital ulcers, eye problems and skin lesions. The condition is named after the Turkish dermatologist Hulusi Behçet who first described the disease in It is also known as Adamantiades–Behçet disease. What causes Behçet disease?