| Literature DB >> 20567567 |
Abstract
Hamartomatous polyposis syndromes are a rare group of hereditary autosomal dominant disorders that comprise less than 1% of all hereditary colorectal cancers. Hamartomatous polyps, in and of themselves, are benign entities; however, these hamartomatous polyposis syndromes have a malignant potential for the development of colorectal cancer as well as extracolonic cancers. Early detection and proper surveillance are vital to minimizing the risk of carcinoma. This article provides a critical review of the clinical presentation, pathology, genetics, and screening and surveillance guidelines of juvenile polyposis syndrome, PTEN hamartoma tumor syndrome, and Peutz-Jeghers syndrome.Entities:
Keywords: Hamartomatous polyposis syndromes; PTEN hamartoma tumor syndrome; Peutz-Jeghers syndrome; juvenile polyposis syndrome
Year: 2010 PMID: 20567567 PMCID: PMC2886463
Source DB: PubMed Journal: Gastroenterol Hepatol (N Y) ISSN: 1554-7914