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Solitary Peutz-Jeghers Polyp of Jejunum: A Rare Cause of Childhood Intussusception
Akshay B Kalavant1, Prema Menon1, Suvradeep Mitra2
1Department of Pediatric Surgery, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Insights
A rare case of jejunal Peutz-Jeghers polyp in an 8-year-old boy caused intussusception. Laparoscopic surgery successfully removed the solitary polyp, marking a unique pediatric case.
Area of Science:
- Gastroenterology
- Pediatric Surgery
- Medical Genetics
Background:
- Peutz-Jeghers syndrome is a rare genetic disorder characterized by hamartomatous polyps in the gastrointestinal tract and increased cancer risk.
- Intussusception, a serious condition where one part of the intestine slides into another, can be a complication of gastrointestinal polyps.
Observation:
- A solitary jejunal Peutz-Jeghers polyp was identified as the cause of intussusception in an 8-year-old boy.
- This represents an extremely rare presentation, particularly in such a young patient.
Findings:
- The jejunal polyp was successfully excised using laparoscopic-assisted surgery.
- This case is the fourth reported instance of a solitary jejunal Peutz-Jeghers polyp and the youngest patient documented in English literature.
Implications:
- Highlights the importance of considering rare gastrointestinal pathologies in pediatric intussusception cases.
- Emphasizes the potential for Peutz-Jeghers polyps to cause acute surgical emergencies even in the absence of widespread disease.
- Demonstrates the efficacy of minimally invasive surgical techniques in managing pediatric gastrointestinal conditions.
Abstract:
An extremely rare case of solitary jejunal Peutz-Jeghers polyp causing intussusception in an 8-year-old boy is reported. The polyp was excised by laparoscopic-assisted surgery. This appears to be only the fourth and the youngest patient with such a polyp reported in the indexed English language literature.
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