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特发性血小板减少性紫癜合并抗磷脂抗体综合征患者ACS后成功PCI术1例
引用本文:许富康,何益平,彭放,郭航远. 特发性血小板减少性紫癜合并抗磷脂抗体综合征患者ACS后成功PCI术1例[J]. 临床心血管病杂志, 2022, 38(1): 81-84
作者姓名:许富康  何益平  彭放  郭航远
作者单位:绍兴市人民医院(浙江大学绍兴医院)心血管内科 浙江绍兴,312000;绍兴文理学院医学院
基金项目:浙江省公益技术应用社会发展项目(No:LGF18H020009)。
摘    要:
1 病例资料患者,女,71岁,因"胸闷1d,突发晕厥1次"入院.患者本次入院为1d前(上午10时许)活动时出现压迫性胸骨中段胸闷,伴左侧手臂痛,出冷汗,伴头晕恶心,家属急送至我院急诊(约14:00时),患者于急诊门口突发晕厥,心电监护提示心室颤动,立即予心肺复苏、电除颤,10余分钟后好转,急查肌钙蛋白7.52 ng/...

关 键 词:急性心肌梗死  特发性血小板减少性紫癜  抗磷脂抗体综合征  经皮冠状动脉介入治疗

Successful PCI after acute myocardial infarction in a patient with idiopathic thrombocytopenic purpura and antiphospholipid syndrome: one case report
XU Fukang,HE Yiping,PENG Fang,GUO Hangyuan. Successful PCI after acute myocardial infarction in a patient with idiopathic thrombocytopenic purpura and antiphospholipid syndrome: one case report[J]. Journal of Clinical Cardiology, 2022, 38(1): 81-84
Authors:XU Fukang  HE Yiping  PENG Fang  GUO Hangyuan
Affiliation:(Department of Cardiology,Shaoxing People's Hospital,Shaoxing Hospital of zhejiang University,Shaoxing,Zhejiang,312000,China;Shaoxing Wenli Medical College)
Abstract:
Though it is rare idiopathic thrombocytopenic purpura or antiphospholipid syndrome could lead to acute myocardial infarction in patients. Here we present a patient with both idiopathic thrombocytopenic purpura and antiphospholipid syndrome who suffered from acute myocardial infarction. Laboratory tests showed a very low platelet count(26×10;/L). So we started anticoagulating therapy with intravenous unfractionated heparin first together with immunoregulation without antiplatelet. When the platelet count increased to more than 50×10;/L, percutaneous coronary intervention was performed in the stenotic coronary artery. There was no recurrence of chest pain, no bleeding or thrombotic events after the stenting or during the follow-up.
Keywords:acute myocardial infarction  idiopathic thrombocytopenic purpura  antiphospholipid syndrome  percutaneous coronary intervention
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