Percutaneous coronary intervention in a case of afibrinogenemia

Asian Cardiovasc Thorac Ann. 2013 Jun;21(3):358-9. doi: 10.1177/0218492312455180.

Abstract

Congenital afibrinogenemia is a rare autosomic recessive blood disorder. A 30-year-old lady, known to have congenital afibrinogenemia, presented with acute anterior myocardial infarction. We managed her with dual antiplatelet therapy and atorvastatin, but her chest pain did not subside and she was transferred to the catheterization laboratory. A proximal left anterior descending artery occlusion was crossed with a floppy wire. Angioplasty was performed successfully with a bare metal stent, and her symptoms resolved completely.

Keywords: Afibrinogenemia; angioplasty; blood coagulation disorders; inherited; myocardial infarction; stents.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Afibrinogenemia / blood
  • Afibrinogenemia / complications
  • Afibrinogenemia / congenital*
  • Afibrinogenemia / diagnosis
  • Angioplasty, Balloon, Coronary* / adverse effects
  • Angioplasty, Balloon, Coronary* / instrumentation
  • Anterior Wall Myocardial Infarction / complications
  • Anterior Wall Myocardial Infarction / diagnosis
  • Anterior Wall Myocardial Infarction / therapy*
  • Anticoagulants / therapeutic use
  • Drug Therapy, Combination
  • Female
  • Hemorrhage / etiology
  • Humans
  • Hydroxymethylglutaryl-CoA Reductase Inhibitors / therapeutic use
  • Platelet Aggregation Inhibitors / therapeutic use
  • Risk Factors
  • Stents
  • Treatment Outcome

Substances

  • Anticoagulants
  • Hydroxymethylglutaryl-CoA Reductase Inhibitors
  • Platelet Aggregation Inhibitors