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Intraluminal Diverticular Duodenal Duplication With Recurrent Abdominal Pain: A Case Report
Jie Chen1, Guo-Zuo Xiong1, Xiong Tan1
1Department of Vascular Surgery, The Second Affiliated Hospital, Hengyang Medical School, University of South China, Hengyang, China.
Insights
Intraluminal diverticular duodenal duplication (IDDD) is a rare congenital anomaly causing recurrent abdominal pain in children. Surgical excision successfully treated a case in an 11-year-old boy, resolving symptoms.
Area of Science:
- Pediatric Surgery
- Gastroenterology
- Congenital Anomalies
Background:
- Duodenal duplication is a rare congenital anomaly.
- It can present with various gastrointestinal symptoms including abdominal pain, bleeding, and obstruction.
- Intraluminal diverticular duodenal duplication (IDDD) is an exceptionally rare subtype.
Observation:
- An 11-year-old boy experienced recurrent abdominal pain.
- Diagnostic imaging, including upper endoscopy and barium swallow, identified a large hole-like structure in the duodenal bulb.
- Operative findings and histopathology confirmed the diagnosis of IDDD.
Findings:
- The patient underwent subtotal excision and duodenal anastomosis for the IDDD.
- The surgical procedure was successful, with no significant postoperative complications.
- Histopathological examination confirmed the diagnosis of duodenal duplication.
Implications:
- This case highlights the importance of considering rare congenital anomalies in pediatric patients with recurrent abdominal pain.
- Early diagnosis and surgical intervention can lead to favorable outcomes.
- Successful management of IDDD can significantly improve a child's quality of life by alleviating chronic symptoms.
Abstract:
Duodenal duplication is a rare congenital anomaly and may manifest as pancreatitis, gastrointestinal bleeding, abdominal pain, perforation, and obstruction. Here, we present a case of intraluminal diverticular duodenal duplication (IDDD) in a child with recurrent abdominal pain caused by a large hole-like structure in the duodenal bulb. This condition has rarely been reported. An 11-year-old boy presented with recurrent attacks of abdominal pain. Upper endoscopy examination and barium swallowing led to an initial diagnosis of IDDD; this diagnosis was confirmed by operative findings and histopathological signs. He underwent a subtotal excision and duodenal anastomosis. No serious complications occurred following treatment. The patient was followed up for 8 months, and his condition improved without symptoms.
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