Juvenile polyposis syndrome
- PMID: 31998494
- PMCID: PMC6982494
- DOI: 10.1002/ccr3.2616
Juvenile polyposis syndrome
Abstract
Juvenile polyposis syndrome (JPS) patients can have a significantly high burden of polyposis. Patient who undergoes prophylactic colectomy for polyps not amenable to endoscopic treatments requires close clinical surveillance to negate risk of malignancy from interval polyposis.
Keywords: adenomatous polyps; colorectal cancer syndromes; hereditary polyposis; juvenile polyps.
© 2019 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd.
Conflict of interest statement
None declared.
Figures
References
-
- Howe JR, Roth S, Ringold JC, et al. Mutations in the SMAD4/DPC4 gene in juvenile polyposis. Science. 1998b;280:1086‐1088. - PubMed
-
- O'Malley M, LaGuardia L, Kalady MF, et al. The prevalence of hereditary hemorrhagic telangiectasia in juvenile polyposis syndrome. Dis Colon Rectum. 2012;55:886‐892. - PubMed
-
- Latchford AR, Neale K, Phillips RK, Clark SK. Juvenile polyposis syndrome: a study of genotype, phenotype, and long‐term outcome. Dis Colon Rectum. 2012;55:1038‐1043. - PubMed
Publication types
LinkOut - more resources
Full Text Sources