Polyp Characteristics of Nonsyndromic and Potentially Syndromic Juvenile Polyps: A Retrospective Cohort Analysis
Nadia Ibrahimi1, Seth S Septer2, Brian R Lee3
1Department of Pediatric Gastroenterology, Children's Mercy Hospital, Kansas City, MO.
Insights
Juvenile polyps (JPs) in children show increased recurrence with higher polyp burden. Adenomatous changes in JPs suggest potential malignancy, independent of polyp number, but are not a biomarker for syndromic disease.
Area of Science:
- Pediatric Gastroenterology
- Gastrointestinal Pathology
- Oncology
Background:
- Juvenile polyps (JPs) are common in children.
- Limited data exists on polyp burden and neoplastic changes in JPs.
Purpose of the Study:
- To analyze the relationship between polyp burden and recurrence in children with JPs.
- To investigate the significance of neoplastic changes in JPs.
Main Methods:
- Retrospective review of 213 pediatric patients with nonsyndromic JPs (2003-2017).
- Data included demographics, clinical presentation, colonoscopy findings, and pathology.
- Exclusion of patients with positive family history, gene mutations, or >10 polyps.
Main Results:
- Polyp recurrence significantly increased with polyp burden (1.5% for 1 polyp, 19.2% for 2-4, 82.6% for 5-10).
- Adenomatous foci were found in 12% of JPs, more common in proximal locations.
- Adenomatous transformation did not correlate with polyp number or recurrence risk.
Conclusions:
- JP recurrence is strongly linked to polyp burden.
- Adenomatous changes in JPs indicate potential malignancy, regardless of the number of polyps.
- Adenomatous transformation in JPs is not a reliable biomarker for syndromic juvenile polyposis.
Background:
Juvenile polyps (JPs) are the most common gastrointestinal polyps diagnosed in children. There is paucity of evidence differentiating polyp burden groups and the presence and significance of neoplastic changes.
Methods:
A retrospective chart review of patients, ages birth through 18 years with nonsyndromic JPs was performed from 2003 to 2017. Abstracted data included basic demographics, age, clinical presentation, colonoscopy findings, and pathology report. Slides of polyps with neoplasia were reviewed by a pathologist.
Results:
A total of 213 subjects underwent 326 procedures and 435 polypectomies. Subjects with positive family history, positive gene mutations, or numerous (>10) polyps were excluded. Groups were defined by polyp number (1, 2-4, 5-10). Polyp recurrence on repeat colonoscopy was significantly related to polyp burden (1 polyp: 1.5%/2-4 polyps 19.2%/5-10 polyps 82.6%: P < 0.001). Polyp distribution was significantly different amongst different groups with isolated polyps favoring a distal distribution. JPs harboring adenomatous foci were reported in 26 (12%) patients. JPs harboring adenomatous foci were significantly more likely to be proximally distributed but the presence of adenomatous transformation within the polyps did not correlate with polyp number or the likelihood of polyp recurrence on repeat colonoscopy.
Conclusions:
JP recurrence is positively and significantly related to polyp burden. JP harbored adenomatous changes independent of polyp number, underscoring a possible malignant potential in JPs. In the absence of a consistent genotype or pedigree, the presence of adenomatous transformation within JPs cannot be construed as a biomarker for syndromic juvenile polyposis.
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