Coronary thrombosis and myocardial infarction as the initial manifestation of protein C deficiency in a 20-year-old man

Heart Lung. 2011 Jul-Aug;40(4):e112-4. doi: 10.1016/j.hrtlng.2010.07.015. Epub 2011 Apr 9.

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.

Publication types

  • Case Reports

MeSH terms

  • Aspirin / therapeutic use
  • Clopidogrel
  • Coronary Thrombosis / diagnosis
  • Coronary Thrombosis / drug therapy
  • Coronary Thrombosis / pathology*
  • Fibrinolytic Agents / therapeutic use
  • Humans
  • Male
  • Myocardial Infarction / diagnosis
  • Myocardial Infarction / drug therapy
  • Myocardial Infarction / pathology*
  • Platelet Aggregation Inhibitors / therapeutic use
  • Protein C Deficiency / complications*
  • Protein C Deficiency / diagnosis
  • Ticlopidine / analogs & derivatives
  • Ticlopidine / therapeutic use
  • Time Factors
  • Warfarin / therapeutic use
  • Young Adult

Substances

  • Fibrinolytic Agents
  • Platelet Aggregation Inhibitors
  • Warfarin
  • Clopidogrel
  • Ticlopidine
  • Aspirin