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Laparoscopic Repair of Para-Esophageal Hernia Using Absorbable Biosynthetic Mesh
Published on: September 11, 2021
Diaphragmatic defect with peritoneopericardial communication
1Division of Cardiothoracic Surgery, Our Lady of Lourdes Medical Center, Camden, New Jersey 08103, USA. asolearchyk@yahoo.com
Insights
This case study details the successful surgical repair of a rare congenital diaphragmatic defect with omental herniation, alongside critical aortic valve stenosis and coronary artery disease in an elderly patient.
Area of Science:
- Cardiothoracic Surgery
- Congenital Diaphragmatic Abnormalities
- Advanced Cardiac Procedures
Background:
- Congenital defects of the diaphragm, particularly peritoneopericardial communication, are rare and can present with complex comorbidities.
- Simultaneous management of diaphragmatic defects, severe aortic stenosis, and coronary artery disease poses significant surgical challenges.
Observation:
- An 81-year-old male presented with a congenital defect of the central tendon of the diaphragm, leading to omental herniation into the pericardial sac.
- The patient also had a critically stenosed congenital bicuspid aortic valve and severe coronary artery disease.
Findings:
- The patient underwent a multi-procedural surgery including omental reduction, coronary artery bypass grafting, aortic valve replacement, and diaphragmatic defect repair.
- Post-operative follow-up at three years showed a well-functioning aortic valve and no recurrence of omental herniation.
Implications:
- This case highlights the feasibility and positive outcomes of complex, multi-stage surgical interventions in elderly patients with multiple congenital and acquired cardiovascular conditions.
- Successful management underscores the importance of addressing all coexisting pathologies for long-term patient well-being.
Abstract:
An 81-year-old man had a congenital defect of the central tendon of the diaphragm, including a peritoneopericardial communication with herniation of the omentum to the pericardial sac in front of the heart. In addition, he had a critically stenosed congenital bicuspid aortic valve and severe coronary artery disease. The patient underwent reduction of the herniated omentum into the abdominal cavity, coronary artery bypass grafting, aortic valve replacement, and closure of the peritoneopericardial communication with a synthetic patch. Three years later, the patient was doing well, with a normally functioning pericardial valve in the aortic position and no sign of omentum around the heart.
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