JACC: Case Reports (Feb 2020)

Pulmonary Arteriovenous Malformation and Embolic Myocardial Infarction in a Patient With Hereditary Hemorrhagic Telangiectasia

  • Gabriel Sánchez-Fernández, MD,
  • Fernando García-López, MD,
  • Isaac Martínez-Bendayán, MD, PhD,
  • María José Bello-Peón, MD,
  • Raquel Marzoa-Rivas, MD, PhD

Journal volume & issue
Vol. 2, no. 2
pp. 316 – 318

Abstract

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This report describes a case of embolic myocardial infarction secondary to a pulmonary arteriovenous malformation. Pulmonary arteriovenous malformations are rare and mostly congenital and are inherited as an autosomal dominant disorder known as hereditary hemorrhagic telangiectasia. Myocardial infarction is an uncommon complication in patients with untreated pulmonary arteriovenous malformations. (Level of Difficulty: Advanced.)

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