Cardiovascular Department, Pars General Hospital, Tehran, Iran.
Heart Lung. 2011 Jul-Aug;40(4):e112-4. doi: 10.1016/j.hrtlng.2010.07.015. Epub 2011 Apr 9.
We report on a 20-year-old man who presented with an extensive acute anteroseptal myocardial infarction (from a thrombotic occlusion of the left anterior coronary artery) as the initial manifestation of hereditary protein C deficiency. This case report, along with previous reports, indicates that a diagnosis of protein C deficiency in young patients with myocardial infarctions is essential for more appropriate management and for the prevention of recurrent events. Furthermore, family screening could lead to a prophylactic approach in carriers of this mutation.
我们报告了一例 20 岁男性,以广泛的急性前间隔心肌梗死(左前冠状动脉血栓性闭塞)为首发表现,存在遗传性蛋白 C 缺乏症。本病例报告和以往报告表明,对于心肌梗死的年轻患者,诊断蛋白 C 缺乏症对于更恰当的管理和预防复发事件至关重要。此外,对这种突变携带者进行家族筛查可能会采取预防性措施。