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Clinical, Endoscopic, and Pathologic Spectrum of Pediatric Polyps: A Single-Center Study in the Current Polypectomy
Sevim Çakar1, Betül Aksoy1, Oğuzhan Akyaz1
1Department of Pediatrics, Division of Pediatric Gastroenterology, Faculty of Medicine, Dokuz Eylül University, Izmir 35340, Turkey.
Pediatric gastrointestinal polyps can be associated with polyposis syndromes, affecting over a quarter of young patients. Comprehensive evaluation, including genetic referral, is crucial for early diagnosis and management of these conditions.
Area of Science:
- Pediatric Gastroenterology
- Gastrointestinal Pathology
- Clinical Genetics
Background:
- Pediatric gastrointestinal polyps are diverse, ranging from benign to syndromic forms with malignant potential.
- Contemporary data on upper GI and small-bowel polyps in children are limited.
- This study highlights an unusually high prevalence of polyposis syndromes in a pediatric cohort.
Purpose of the Study:
- To provide contemporary data on pediatric gastrointestinal polyps, including upper GI and small-bowel.
- To determine the prevalence of polyposis syndromes in children diagnosed with gastrointestinal polyps.
- To identify clinical and histopathological factors associated with polyposis syndromes in pediatric patients.
Main Methods:
- Retrospective single-center study of children (0-18 years) with gastrointestinal polyps.
- Data collected: demographics, symptoms, endoscopic features, histopathology, management, and polyposis syndrome status.
- Statistical analysis using IBM SPSS Statistics, with p < 0.05 significance.
Main Results:
- Seventy-six pediatric patients evaluated; gastrointestinal bleeding was the most common symptom.
- Juvenile and inflammatory polyps were the most frequent histologic subtypes.
- Polyposis syndromes identified in 27.6% of patients, associated with multiple, proximal, or mixed-morphology polyps.
Conclusions:
- Pediatric gastrointestinal polyps are not uniformly benign, with a significant prevalence of associated polyposis syndromes.
- Comprehensive endoscopic evaluation, routine histopathology, and genetic referral are recommended.
- Early identification of syndromic forms is critical for appropriate management.
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