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Updated: Jun 26, 2026

Laparoscopic Choledochal Cyst Excision and Roux-en-Y Choledochojejunostomy in Adults
Published on: February 28, 2025
Acquired duodenal obstruction in children
Jen-Hung Chien1, Tsyr-Yuh Ho, Lin Shih-Peng
1Department of Pediatrics, Zuoying Armed Forces General Hospital, Kaohsiung, Taiwan.
Insights
Pediatric duodenal obstruction can stem from rare causes like traumatic intramural hematoma or duodenal webs. Early diagnosis and intervention are crucial for favorable outcomes in children.
Area of Science:
- Pediatric Surgery
- Gastrointestinal Disorders
- Trauma Surgery
Background:
- Acquired proximal gastrointestinal obstruction in children is uncommon.
- High index of suspicion is needed for early diagnosis of rare causes.
- Blunt abdominal trauma and duodenal webs are potential etiologies.
Observation:
- A 6-year-old boy presented with epigastric pain and bilious vomiting after bicycle handlebar trauma.
- Imaging revealed a large duodenojejunal hematoma, unresponsive to conservative management.
- A 2-year-old girl presented with acute proximal intestinal obstruction due to a duodenal web with a bezoar.
Findings:
- Laparoscopic hematoma evacuation was required for the traumatic case.
- Surgical removal of the bezoar and duodenoduodenostomy resolved the obstruction in the web case.
- Both children experienced successful recovery and resumed feeding.
Implications:
- Traumatic intramural hematoma and duodenal webs should be considered in pediatric proximal gastrointestinal obstruction.
- Prompt diagnosis and surgical intervention can lead to positive outcomes.
- This highlights the importance of considering rare conditions in pediatric surgical emergencies.
Abstract:
Traumatic intramural hematoma of the duodenum is a rare cause of acquired duodenal obstruction in children, and a high degree of suspicion is therefore required to make an early and accurate diagnosis. We report a 6-year-old boy whose epigastrium was impacted by the handlebar of his bicycle during a traffic accident. The boy then experienced epigastralgia. Six days later, progressive bilious vomiting suggestive of gastrointestinal obstruction was noted. Imaging studies revealed a large hematoma extending from the fourth portion of the duodenum to the jejunum. Conservative methods of treatment failed to manage his condition. He underwent laparoscopic surgery to evacuate the hematoma. We also report a case of duodenal obstruction in a previously healthy 2-year-old girl who presented for the first time with acute symptoms of proximal intestinal obstruction. Contrast examinations showed apparent barium retention over the stomach and proximal duodenum. She underwent surgery due to persistent obstruction, and a mushroom-like foreign body was detected embedded in the orifice of the windsock duodenal web. After duodenoduodenostomy and removal of the bezoar, she had a smooth recovery and tolerated feeding well. We conclude that blunt abdominal trauma and incomplete duodenal obstruction, such as that caused by duodenal web, should be considered as possible causes of acquired proximal gastrointestinal obstruction in previously healthy children, despite their rarity.
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