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Congenital diaphragmatic hernia: an unusual cause of obstructive jaundice
1Department of Surgery, Royal Gwent Hospital, Newport, UK. huwgjones@hotmail.com
Insights
Congenital diaphragmatic hernias are rare in adults. This case highlights obstructive jaundice caused by a Bochdalek hernia, emphasizing the need for timely diagnosis and management.
Area of Science:
- Gastroenterology and Hepatology
- Thoracic Surgery
- Medical Diagnostics
Background:
- Congenital diaphragmatic hernias (CDH) are rare in the adult population.
- Typical presentations include dyspnea, gastric reflux, and intestinal obstruction.
Observation:
- A young woman presented with obstructive jaundice.
- The jaundice was found to be secondary to a Bochdalek hernia of the right hemidiaphragm.
Findings:
- Bochdalek hernias can present atypically in adults, leading to conditions like obstructive jaundice.
- Diagnostic imaging is crucial for identifying diaphragmatic defects in adults.
Implications:
- This case underscores the importance of considering rare diagnoses in adult patients with gastrointestinal and biliary symptoms.
- Early recognition and surgical intervention are key for favorable outcomes in adult CDH.
Abstract:
Congenital diaphragmatic hernias in adults are exceedingly rare. They have been reported to cause dyspnoea, gastric reflux and intestinal obstruction. We present the case of a young woman with obstructive jaundice secondary to a Bochdalek hernia of the right hemidiaphragm. We discuss the aetiologies, presentation, investigation and treatment of the disorder, and make recommendations on the management.
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