Crisscross heart-Morphology, clinical diagnosis, and management options

Trushar Gajjar1, Jinaga Nageswar Rao1, Neelam Desai1

  • 1Department of Cardiothoracic and Vascular Surgery, Sri Sathya Sai Institute of Higher Medical Sciences, Prashanthigram, Andhra Pradesh, India.

Journal of Cardiac Surgery
|November 19, 2016
PubMed

Insights

Crisscross heart, a rare congenital heart defect, involves twisted ventricles. This study reports a unique case with situs inversus and other anomalies, highlighting the rarity of this cardiac malformation.

Area of Science:

  • Cardiology
  • Developmental Biology
  • Medical Genetics

Background:

  • Crisscross heart is a rare congenital cardiac malformation.
  • It is characterized by the crossing of ventricular inflow streams due to cardiac torsion.
  • The developmental mechanisms and etiology remain largely unknown.

Observation:

  • This study presents a rare case of crisscross heart in a neonate.
  • The patient exhibited situs inversus, concordant atrioventricular and ventriculoarterial connections.
  • Additional anomalies included a ventricular septal defect and pulmonary stenosis.

Findings:

  • The case demonstrates a complex presentation of crisscross heart with multiple associated anomalies.
  • Literature review indicates the extreme rarity of this condition, especially with situs inversus.
  • The findings contribute to understanding the spectrum of crisscross heart malformations.

Implications:

  • This case expands the known phenotypic spectrum of crisscross heart.
  • Further research into the developmental pathways is needed to elucidate causes.
  • Improved understanding may aid in diagnosis and management of rare cardiac malformations.

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