Abstract
Twelve of 45 patients with multiple myeloma had abnormal conversion of fibrinogen to fibrin as evidenced by a prolonged thrombin time. In its most striking form the abnormality consists of a markedly delayed conversion of fibrinogen to a homogeneous, gelatinous clot without histologic evidence of fibrin threads. The abnormal proteins accounting for this phenomenon were present in the beta- and gamma-globulin fractions of two patients studied in detail. Clinically, only the severest form of this abnormality caused hemorrhagic symptoms.