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Acquired Pediatric Right Diaphragmatic Hernia Following Automatic Implantable Cardioverter-defibrillator Placement
Adria Ottoboni1, Larissa Morsky1, Laura C Castro1
1Kern Medical Center, Department of Emergency Medicine, Bakersfield, California.
Insights
Diaphragmatic hernias are rare in children but can be fatal if diagnosis is delayed. This case highlights key radiographic and clinical findings in a one-year-old patient, emphasizing early detection for better outcomes.
Area of Science:
- Pediatric Surgery
- Diagnostic Imaging
- Congenital Abnormalities
Background:
- Diaphragmatic hernias are uncommon congenital defects in infants and children.
- Delayed diagnosis of pediatric diaphragmatic hernias can lead to severe complications, including high morbidity and mortality.
- Accurate and timely diagnosis is critical for effective management.
Purpose of the Study:
- To present a case study of a pediatric diaphragmatic hernia.
- To illustrate the diagnostic utility of radiographic and clinical examination findings.
- To emphasize the importance of early recognition in managing this condition.
Main Methods:
- Case report of a one-year-old patient.
- Review of clinical presentation and physical examination findings.
- Analysis of radiographic imaging (e.g., X-ray, CT scan) for diagnostic clues.
Main Results:
- The case details the specific radiographic features suggestive of diaphragmatic hernia.
- Clinical examination findings correlated with imaging results.
- The diagnosis was confirmed, allowing for timely intervention.
Conclusions:
- Diaphragmatic hernias require a high index of suspicion in pediatric patients.
- Radiographic and clinical assessments are crucial for prompt diagnosis.
- Early detection and management significantly improve patient outcomes and reduce mortality.
Abstract:
Diaphragmatic hernias are an uncommon occurrence in the pediatric population; however, they can cause significant morbidity and mortality if the diagnosis is missed or delayed. This case discusses the radiographic and clinical exam findings of a one-year-old patient with this pathology.
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