Gouri Adel, Yakhlef Amina, Dekaken Aoulia, Bentorki Ahmed Aymen
Laboratory of medical biochemistry, IBN Zohr Hospital, Guelma, Algeria.
Ann Biol Clin (Paris). 2012 Jul-Aug;70(4):489-91. doi: 10.1684/abc.2012.0735.
The occurrence of myocardial infarction in myeloproliferative disease is mostly attributed to coronary thrombosis due to hyperviscosity and thrombocytosis. We report a 55-year-old man case with polycythemia vera none diagnosed before and revealing with ST-segment elevation myocardial infarction; this is a relative rare association. The clinical status, comorbidities and patient outcome were studied. This case illustrates the importance of early diagnosis of polycythemia vera and research almost systemic thrombotic complications.
骨髓增殖性疾病中心肌梗死的发生大多归因于高黏滞血症和血小板增多症导致的冠状动脉血栓形成。我们报告一例55岁男性病例,其患有真性红细胞增多症,此前未被诊断出,此次因ST段抬高型心肌梗死而被发现;这是一种相对罕见的关联情况。我们对其临床状况、合并症及患者预后进行了研究。该病例说明了早期诊断真性红细胞增多症以及研究几乎全身性血栓并发症的重要性。