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Criss-cross heart--a case with horizontal septum, complete transposition, pulmonary atresia and ventricular septal

Pediatric Cardiology
|January 1, 1982
PubMed

Insights

Criss-cross heart, a rare anomaly, involves crossing blood streams at the atrioventricular level without mixing. This case presents a unique combination of cardiac defects, including d-transposition of the great arteries and pulmonary atresia.

Area of Science:

  • Cardiology
  • Pediatric Cardiology
  • Congenital Heart Disease

Background:

  • Criss-cross heart is a rare congenital anomaly characterized by the crossing of systemic and pulmonary blood streams at the atrioventricular (AV) level without intracardiac mixing.
  • Understanding the anatomical variations and associated defects is crucial for diagnosis and management.

Observation:

  • A case of criss-cross heart is presented with a solitus right atrium connected to a left-superior, morphologically right ventricle.
  • The left atrium was connected to a normally positioned, morphologically left ventricle, with the interventricular septum in a horizontal plane.
  • Associated anomalies included complete d-transposition of the great arteries with l-positioned aorta, pulmonary atresia, ventricular septal defect, atrial septal defect, and patent ductus arteriosus.

Findings:

  • This report provides the first angiocardiographic demonstration of this rare combination of congenital heart defects.
  • The study reviews existing literature on criss-cross heart and horizontal interventricular septum.
  • The findings emphasize the recognition of criss-cross heart as an established angiocardiographic entity.

Implications:

  • This detailed case report contributes to the understanding of complex congenital heart anomalies.
  • Accurate angiocardiographic recognition of criss-cross heart is vital for appropriate clinical management and surgical planning.
  • Further research into the embryological basis and long-term outcomes of criss-cross heart is warranted.

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