2.6 Other
Behcet disease: an atypical DVT. Diagnosis and treatment. M. Bouayed Behcet’s disease (BD) is a primitive multisystematic vasculitis nonautoimmune disease of unknown etiology. It is exceptional after the age of 60 and common in the Mediterranean basin and in Japan. The International Clinical Criteria from 1990 are recurrent oral ulcers, recurrent ulcers more than three times in 12 months, and two of the following: recurrent genital ulcerations, eye-injury, skin-lesions, and a positive pathergy test (sensitivity, 91% and specificity, 96%). The vascular lesions are highly suggestive of an attack on the arteries and veins of any caliber. In the vascular lesions,…