Juvenile Hamartomatous Polyp Causing Jejunal Intussusception in an Eight-Year-Old Child: A Case Report.
AI interpretation is pending for this paper.
Open original publication →What the AI sees
Not AI summarized yet.
Research significance
Pending deeper interpretation.
Source abstract
While juvenile hamartomatous polyps are common pediatric findings, they are almost exclusively restricted to the colon and rectum; their occurrence in the small intestine is exceptionally rare and presents a significant diagnostic dilemma. This case report describes an eight-year-old patient who presented with vague constitutional symptoms, including intermittent vomiting, abdominal pain, and severe weight loss resulting in a Z-score of -3.29. Initial diagnostic investigations, including abdominal ultrasound, computed tomography, upper digestive endoscopy, and contrast bowel studies, failed to identify a clear etiology. Following an exploratory laparotomy, a juvenile hamartomatous polyp was identified in the mid-jejunum, acting as a lead point for intermittent intussusception with secondary vascular congestion of the intestinal loops. The diagnosis was confirmed through anatomopathological analysis after a successful enterectomy. This case demonstrates that in the presence of unexplained malnutrition and cyclical emesis, clinicians must maintain a high index of suspicion for small bowel lesions, as prompt surgical intervention can prevent further complications and lead to complete symptomatic resolution.