Left-Sided Congenital Diaphragmatic Hernia with Multiple Congenital Cardiac Anomalies, Hernia Sac, and Microscopic Hepatic Heterotopia: A Case Report
2011

Case Report of Congenital Diaphragmatic Hernia with Cardiac Anomalies

Sample size: 1 publication Evidence: low

Author Information

Author(s): Arafah Maria, Boqari Deena T., Alsaad Khaled O.

Primary Institution: King Khalid University Hospital, College of Medicine, King Saud University, Saudi Arabia

Hypothesis

The study investigates the occurrence of microscopic heterotopic hepatic tissue in congenital diaphragmatic hernia associated with cardiac anomalies.

Conclusion

The case highlights the presence of microscopic heterotopic hepatic tissue in a congenital diaphragmatic hernia, which is rarely reported.

Supporting Evidence

  • Congenital diaphragmatic hernia is a common congenital anomaly with an incidence of 1 in 2000 to 1 in 5000 live births.
  • Associated congenital anomalies are present in 30 to 40% of CDH cases.
  • Microscopic heterotopic hepatic tissue in CDH is a very uncommon finding.

Takeaway

This study talks about a baby who had a hole in his diaphragm and some liver tissue in the wrong place, along with heart problems.

Methodology

The case report details the clinical presentation, surgical intervention, and histological examination of the tissue.

Limitations

The findings are based on a single case report, limiting generalizability.

Participant Demographics

A full-term infant boy.

Digital Object Identifier (DOI)

10.4061/2011/967107

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