Currimbhoy Z, Vinciguerra V, Palakavongs P, Kuslansky P, Degnan T J
Am J Clin Pathol. 1976 Jun;65(6):970-4. doi: 10.1093/ajcp/65.6.970.
The case of a patient who, while being treated for an acute myocardial infarction, was found to have Fletcher factor deficiency with a Fletcher factor concentration of less than 1% of normal is described. Fletcher factor deficiency is associated with defects in several interrelated systems, including clotting, fibrinolysis and kinin generation, all of which play a role in the pathogenesis and evolution of infarction. The development of myocardial infarction in a patient who had severe Fletcher factor deficiency emphasizes the importance of alternate pathways for activation of these systems.
本文描述了一名在治疗急性心肌梗死时被发现弗莱彻因子缺乏且其浓度低于正常水平1%的患者的病例。弗莱彻因子缺乏与包括凝血、纤维蛋白溶解和激肽生成在内的几个相互关联系统的缺陷有关,所有这些系统在梗死的发病机制和演变过程中都发挥着作用。一名患有严重弗莱彻因子缺乏的患者发生心肌梗死,这强调了激活这些系统的替代途径的重要性。