【摘 要】
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INTRODUCTIONArrhythmogenic right ventricular cardiomy-opathy/dysplasia (ARVC/D) is characterized by progressive fibro-fatty replacement of cardi-ac myocytes in
【机 构】
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Reproductive Center,The Sixth Affiliated Hospital of Sun Yat-sen University,Guangzhou 510655“,”Depar
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INTRODUCTIONArrhythmogenic right ventricular cardiomy-opathy/dysplasia (ARVC/D) is characterized by progressive fibro-fatty replacement of cardi-ac myocytes in both ventricles,with the risk of heart failure and sudden death 1,2. Systemic thromboembolism,including pulmonary em-bolism and cerebral infarction,was an essen-tial risk of worsening prognosis of ARVC/D, which was not related to ventricular arrhyth-mia 3-5. Especially,ventricular dysfunction andaneurysm would further increase the risk of thrombosis 6. Our study would report a case of ARVC/D occurred with massive cerebral in-farction without oral anticoagulation. Further-more, we reviewed the previous reports of thromboembolic complications of ARVC/D and thus emphasized the importance of antico-agulant therapy in ARVC/D patients.
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