| Literature DB >> 26676416 |
Keisuke Hata1, Yoko Yamamoto1, Tomomichi Kiyomatsu1, Toshiaki Tanaka1, Shinsuke Kazama1, Hiroaki Nozawa1, Kazushige Kawai1, Junichiro Tanaka1, Takeshi Nishikawa1, Kensuke Otani1, Koji Yasuda1, Junko Kishikawa1, Yuzo Nagai1, Hiroyuki Anzai1, Takahide Shinagawa1, Keiichi Arakawa1, Hironori Yamaguchi1, Soichiro Ishihara1, Eiji Sunami1, Joji Kitayama1, Toshiaki Watanabe2.
Abstract
Gastrointestinal (GI) cancer, including gastric and colorectal cancer, is a major cause of death worldwide. A substantial proportion of patients with GI cancer have a familial history, and several causative genes have been identified. Gene carriers with these hereditary GI syndromes often harbor several kinds of cancer at an early age, and genetic testing and specific surveillance may save their lives through early detection. Gastroenterologists and GI surgeons should be familiar with these syndromes, even though they are not always associated with a high penetrance of GI cancer. In this review, we provide an overview and discuss the diagnosis, genetic testing, and management of four major hereditary GI cancers: familial adenomatous polyposis, Lynch syndrome, hereditary diffuse gastric cancer, and Li-Fraumeni syndrome.Entities:
Keywords: Familial adenomatous polyposis; Hereditary diffuse gastric cancer; Li–Fraumeni syndrome; Lynch syndrome
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Year: 2015 PMID: 26676416 DOI: 10.1007/s00595-015-1283-3
Source DB: PubMed Journal: Surg Today ISSN: 0941-1291 Impact factor: 2.549