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Atrioventricular septal defect with cor triatriatum sinister

Yu-Yin Liu1, Yao-Kuang Huang, Chi-Nan Tseng

  • 1Division of Thoracic and Cardiovascular Surgery, Chang Gung Memorial Hospital, Taipei, ROC.

Chang Gung Medical Journal
|September 1, 2007
PubMed

Insights

Cor triatriatum with complete atrioventricular septal defect is a rare congenital heart defect. This case study details successful surgical repair in an infant, achieving normal cardiac function post-operation.

Area of Science:

  • Cardiology
  • Congenital Heart Disease
  • Pediatric Cardiac Surgery

Background:

  • Cor triatriatum (CT) is a rare cardiac anomaly involving left atrial partitioning.
  • Association of CT with atrioventricular septal defects (AVSD) is exceptionally uncommon.
  • Few cases of CT combined with complete AVSD have been previously documented.

Observation:

  • An 11-month-old female infant presented with a rare combination of complete atrioventricular septal defect and cor triatriatum.
  • The infant underwent surgical correction for both cardiac anomalies.

Findings:

  • The patient experienced an uneventful recovery following surgical intervention.
  • Normal cardiac performance was successfully restored 2 years after the surgery.

Implications:

  • This case highlights the feasibility of surgical correction for complex congenital heart defects like CT and complete AVSD in infants.
  • Successful surgical outcomes underscore the importance of early diagnosis and intervention for rare cardiac anomalies.
  • Further research into the management of combined CT and AVSD may improve clinical guidelines and patient outcomes.

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