ArticleFrontiers in pediatrics2025
Inflammatory myofibroblastic tumor of the ileocecal area complicated by intussusception: a case report in a child.
Article in Frontiers in pediatrics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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1 citing paper in PubMed.
- A Rare Case of Pediatric Gastric Inflammatory Myofibroblastic Tumor (IMT) Mimicking Gastrointestinal Stromal Tumor (GIST): A Case Report.Clinical case reports · 2026Article
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4 authors.
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Abstract
Inflammatory myofibroblastic tumor (IMT) is a rare mesenchymal tumor that can occur in multiple organs. This case report presented an unusual instance of ileocecal IMT in a child complicated by secondary intussusception. A 2-year-6-month-old male was admitted with abdominal pain and fever for 15 days, progressing to currant jelly stools for 2 days. Physical examination revealed a right abdominal mass, and emergency laparotomy confirmed ileocolic intussusception with a firm mass in the ileocecal region. Pathological examination confirmed the diagnosis of IMT. IMT as a secondary cause in pediatric ileocecal intussusception is rare when encountering an atypical intussusception with a suspect lead-point, IMT should be considered.
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