Behçet's disease is a chronic multi-system disease presenting with recurrent oral and genital ulceration, and relapsing uveitis. Cardiac involvement is an extremely rare manifestation of this disorder. We report an unusual case of Behçet's disease characterized by a mural cardiac thrombi in the right atrium and right ventricle along with transient protein C and S deficiency.
作者：C, Gürgün；A, Sagcan；C S, Cinar；T, Yagdi；M, Zoghi；T, Tekten；H, Kultursay
来源：Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2000 年 11卷 1期
