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Acute myocardial infarction in hemoglobin SC disease
Authors:Henry?Wang,Lawrence?J.?Laslett,Carol?M.?Richman,Ted?Wun  author-information"  >  author-information__contact u-icon-before"  >  mailto:ted.wun@ucdmc.ucdavis.edu"   title="  ted.wun@ucdmc.ucdavis.edu"   itemprop="  email"   data-track="  click"   data-track-action="  Email author"   data-track-label="  "  >Email author
Affiliation:(1) Division of Hematology and Oncology, Department of Medicine, Davis School of Medicine, University of California Davis Cancer Center, Sacramento, CA 95817, USA;(2) Division of Cardiology, Davis School of Medicine, University of California, Sacramento, CA, USA;(3) Section of Hematology and Oncology, VA Northern California Health Care System, Sacramento, CA, USA
Abstract:Although there are reports of myocardial infarction (MI) in patients with sickle cell diseases, an antemortem diagnosis of acute MI in a patient with compound heterozygous hemoglobin SC disease has not been reported. Herein, we present a patient with hemoglobin SC who suffered an acute MI. She had typical chest pain for myocardial ischemia, associated with ST elevations on the electrocardiogram (EKG) and elevations of cardiac injury markers diagnostic of infarction. The patient was treated with conventional therapies for acute coronary syndrome and also emergent red blood cell exchange. Interestingly, coronary angiography was completely normal in this patient. Potential mechanisms and management for acute MI in patients with sickle cell disease are discussed.
Keywords:Hemoglobin SC disease  Myocardial infarction  Diagnosis  Treatment
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