Popliteal Artery Thrombosis in Behçet's Syndrome. A New Manifestation of a Very Little Known Condition

In 1937 Behcet, professor of dermatology at the University of Istanbul, published the first of a series of papers in which he advocated that the triad of relapsing iritis, ulcers of mouth and ulcers of genitalia be considered as a disease entity (1, 2, 3). Since then there has been a tendency to associate his name with the condition. The next landmark appeared in 1946 when Jebejian and Kalfayan (4) reported a case in which they were able to make frequent ophthalmoscopic observations during recurring attacks of uveitis. As a result, it was concluded that the fundamental lesion of the ocular fundus was an inflammatory reaction involving the smallest veins, often accompanied by haemorrhage and at times complicated by a sudden thrombosis. In the same year Curth’s comprehensive review (5) of Beh~et’s disease appeared. She described a man of Italian parentage who showed the complete triad and a woman with ulcers of the mouth and genitalia but without eye lesions. A discussion of case reports containing manifestations other than those of the complete triad was included. We report another clinical case and draw attention to

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[4]  T. Matsumoto,et al.  Clinical Studies on Behçet's Syndrome , 1963, Annals of the rheumatic diseases.

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[6]  H. Curth Recurrent genito-oral aphthosis and uveitis with hypopyon (Behcet's syndrome). , 1946, Archives of dermatology and syphilology.