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    Gastroenterol Hepatol (N Y). 2010 Mar;6(3):185-96.

    Hereditary hamartomatous polyposis syndromes: understanding the disease risks as children reach adulthood.

    Source

    Dr. Manfredi serves as Instructor in Pediatrics at Harvard Medical School and Associate Director of Endoscopy at Children's Hospital Boston in Boston, Massachusetts.

    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.

    PMID:
    20567567
    [PubMed]
    PMCID:
    PMC2886463
    Free PMC Article

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