{"title":"血栓性血小板减少性紫癜相关急性心肌梗死","authors":"B. Türker, S. Ahbab, Fatih Türker, H. E. Ataoğlu","doi":"10.26838/medrech.2018.5.3.407","DOIUrl":null,"url":null,"abstract":"Introduction: Thrombotic thrombocytopenic purpura (TTP) is a rare life-threatening thrombotic microangiopathy. The central nervous system, kidneys, and myocard can be affected by TTP. Case Presentation: A 47-year-old female patient with no chronic disease came to the emergency department presented with chest pain, blur in seeing. Electrocardiogram was performed and there was biphasic T wave pattern. Laboratory tests showed an elevation in white blood cell (14.10/mm), decrease in thrombocyte (3.000/mm). Blood urea nitrogen (BUN) was 129.3 mg/dl, serum creatinine was 1.87 mg/dl, lactate dehydrogenase (LDH) was 1581 U/l. Cardiac markers were elevated. These tests results revealed non ST-elevation myocardial infarction and acute renal injury. Antithrombotic agents were not applied because of thrombocytopenia. ADAMTS 13 activity was found lower than 0, 2 % and ADAMTS 13 antibodies were positive. Plasmapheresis was started to perform, immediately and repeated for ten days. After the treatment, hematologic parameters and LDH values came to normal ranges. Conclusion: Thrombotic Thrombocytopenic Purpura (TTP) is a type of thrombotic microangiopathic anemia. If it is not diagnosed early, the mortality rate can be about 90%. Plasmapheresis should begin immediately.","PeriodicalId":282906,"journal":{"name":"Medico Research Chronicles","volume":"218 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2018-05-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"THROMBOTIC THROMBOCYTOPENIC PURPURA RELATED ACUTE MYOCARDIAL INFARCTION\",\"authors\":\"B. Türker, S. Ahbab, Fatih Türker, H. E. Ataoğlu\",\"doi\":\"10.26838/medrech.2018.5.3.407\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Introduction: Thrombotic thrombocytopenic purpura (TTP) is a rare life-threatening thrombotic microangiopathy. The central nervous system, kidneys, and myocard can be affected by TTP. Case Presentation: A 47-year-old female patient with no chronic disease came to the emergency department presented with chest pain, blur in seeing. Electrocardiogram was performed and there was biphasic T wave pattern. Laboratory tests showed an elevation in white blood cell (14.10/mm), decrease in thrombocyte (3.000/mm). Blood urea nitrogen (BUN) was 129.3 mg/dl, serum creatinine was 1.87 mg/dl, lactate dehydrogenase (LDH) was 1581 U/l. Cardiac markers were elevated. These tests results revealed non ST-elevation myocardial infarction and acute renal injury. Antithrombotic agents were not applied because of thrombocytopenia. ADAMTS 13 activity was found lower than 0, 2 % and ADAMTS 13 antibodies were positive. Plasmapheresis was started to perform, immediately and repeated for ten days. After the treatment, hematologic parameters and LDH values came to normal ranges. Conclusion: Thrombotic Thrombocytopenic Purpura (TTP) is a type of thrombotic microangiopathic anemia. If it is not diagnosed early, the mortality rate can be about 90%. Plasmapheresis should begin immediately.\",\"PeriodicalId\":282906,\"journal\":{\"name\":\"Medico Research Chronicles\",\"volume\":\"218 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2018-05-20\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Medico Research Chronicles\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.26838/medrech.2018.5.3.407\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Medico Research Chronicles","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.26838/medrech.2018.5.3.407","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
THROMBOTIC THROMBOCYTOPENIC PURPURA RELATED ACUTE MYOCARDIAL INFARCTION
Introduction: Thrombotic thrombocytopenic purpura (TTP) is a rare life-threatening thrombotic microangiopathy. The central nervous system, kidneys, and myocard can be affected by TTP. Case Presentation: A 47-year-old female patient with no chronic disease came to the emergency department presented with chest pain, blur in seeing. Electrocardiogram was performed and there was biphasic T wave pattern. Laboratory tests showed an elevation in white blood cell (14.10/mm), decrease in thrombocyte (3.000/mm). Blood urea nitrogen (BUN) was 129.3 mg/dl, serum creatinine was 1.87 mg/dl, lactate dehydrogenase (LDH) was 1581 U/l. Cardiac markers were elevated. These tests results revealed non ST-elevation myocardial infarction and acute renal injury. Antithrombotic agents were not applied because of thrombocytopenia. ADAMTS 13 activity was found lower than 0, 2 % and ADAMTS 13 antibodies were positive. Plasmapheresis was started to perform, immediately and repeated for ten days. After the treatment, hematologic parameters and LDH values came to normal ranges. Conclusion: Thrombotic Thrombocytopenic Purpura (TTP) is a type of thrombotic microangiopathic anemia. If it is not diagnosed early, the mortality rate can be about 90%. Plasmapheresis should begin immediately.