Juvenile Polyps and Juvenile Polyp Syndromes in Children: A Clinical and Endoscopic Survey

被引:20
作者
Hood, Brandy [1 ]
Bigler, Steven [1 ]
Bishop, Phyllis [1 ]
Liu, Hua [1 ]
Ahmad, Naveed [1 ]
Renault, Macey [1 ]
Nowicki, Michael [1 ]
机构
[1] Univ Mississippi, Med Ctr, Div Pediat Gastroenterol, Jackson, MS 39216 USA
关键词
juvenile polyps; juvenile polyposis syndrome; malignant potential; immunohistochemical markers; COLONIC POLYPS; COLONOSCOPIC POLYPECTOMY; GERMLINE MUTATIONS; BMPR1A MUTATIONS; CHILDHOOD; GENE; EXPERIENCE; PHENOTYPE; RECTUM; MADH4;
D O I
10.1177/0009922811407177
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
In children, most colonic polyps are juvenile polyps with negligible risk for malignant transformation. The exception is juvenile polyposis syndrome (JPS) where there is a risk for developing colon cancer. The authors studied differences in clinical features and colonoscopic findings in children with solitary juvenile polyps (SJP), multiple juvenile polyps (MJP), and JPS. Methods. Children were identified as SJP (1 polyp), MJP (2-4 polyps), or JPS (>5 polyps). Demographic data, laboratory values, family history, and colonoscopic findings were recorded. Results. Children having polypectomy had juvenile polyps (93%), adenomatous polyps (5%), and Peutz-Jegher syndrome (3%). Juvenile polyps were classified as SJP (67%), MJP (16%), and JPS (17%). Children with SJP were younger, were more likely to have polyps limited to the rectosigmoid colon, and had larger polyps than children with MJP and JPS. Anemia was more common in JPS than MJP and SJP. Conclusion. Clinical and endoscopic findings differ between SJP, MJP, and JPS.
引用
收藏
页码:910 / 915
页数:6
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