Spontaneous Coronary Artery Dissection Complicated by Left Ventricular Free Wall Rupture in Turner Syndrome

Brendan F Caprio1, Kunal Kotkar2, Alan Zajarias1

  • 1Department of Medicine, Washington University School of Medicine, St. Louis, Missouri, USA.

JACC. Case Reports
|March 2, 2023
PubMed

Insights

Spontaneous coronary artery dissection (SCAD) is a rare cause of heart attack, especially in women with Turner syndrome. This case highlights a unique presentation and successful management of SCAD with left ventricular free wall rupture in a Turner syndrome patient.

Area of Science:

  • Cardiology
  • Genetics
  • Vascular Biology

Background:

  • Turner syndrome is a genetic condition affecting females, associated with cardiovascular risks.
  • Spontaneous coronary artery dissection (SCAD) is an underdiagnosed cause of acute myocardial infarction, particularly in young to middle-aged women.
  • Left ventricular free wall rupture is a rare but catastrophic complication of myocardial infarction.

Observation:

  • A 38-year-old female with Turner syndrome presented with acute myocardial infarction.
  • The myocardial infarction was caused by multivessel spontaneous coronary artery dissection (SCAD).
  • The patient developed a left ventricular free wall rupture, characterized as oozing-type.

Findings:

  • Conservative management was initiated for the spontaneous coronary artery dissection (SCAD).
  • The patient successfully underwent sutureless repair for the left ventricular free wall rupture.
  • This represents the first reported case of SCAD in a patient with Turner syndrome.

Implications:

  • This case expands the known spectrum of cardiovascular complications associated with Turner syndrome.
  • It underscores the importance of considering SCAD in young women presenting with myocardial infarction, even with underlying genetic conditions.
  • The successful sutureless repair technique for left ventricular free wall rupture may offer a novel therapeutic option.

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