Abstract
We report on a 20-year-old man who presented with an extensive acute anteroseptal myocardial infarction (from a thrombotic occlusion of the left anterior coronary artery) as the initial manifestation of hereditary protein C deficiency. This case report, along with previous reports, indicates that a diagnosis of protein C deficiency in young patients with myocardial infarctions is essential for more appropriate management and for the prevention of recurrent events. Furthermore, family screening could lead to a prophylactic approach in carriers of this mutation.
Copyright © 2011 Elsevier Inc. All rights reserved.
MeSH terms
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Aspirin / therapeutic use
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Clopidogrel
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Coronary Thrombosis / diagnosis
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Coronary Thrombosis / drug therapy
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Coronary Thrombosis / pathology*
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Fibrinolytic Agents / therapeutic use
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Humans
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Male
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Myocardial Infarction / diagnosis
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Myocardial Infarction / drug therapy
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Myocardial Infarction / pathology*
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Platelet Aggregation Inhibitors / therapeutic use
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Protein C Deficiency / complications*
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Protein C Deficiency / diagnosis
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Ticlopidine / analogs & derivatives
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Ticlopidine / therapeutic use
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Time Factors
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Warfarin / therapeutic use
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Young Adult
Substances
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Fibrinolytic Agents
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Platelet Aggregation Inhibitors
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Warfarin
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Clopidogrel
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Ticlopidine
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Aspirin