Two Cases of Lynch Syndrome That Were Diagnosed and Resected as Duodenal Cancer
Author:
Affiliation:
1. Department of Surgery, Kitasato Institute Hospital, Kitasato University
2. Department of Diagnostic Pathology, Kitasato Institute Hospital, Kitasato University
Publisher
The Japanese Journal of Gastroenterological Surgery
Subject
Gastroenterology,Surgery
Link
https://www.jstage.jst.go.jp/article/jjgs/52/1/52_2018.0031/_pdf
Reference17 articles.
1. 2) Lynch HT, Shaw MW, Magnuson CW, Larsen AL, Krush AJ. Hereditary factors in cancer. Study of two large midwestern kindreds. Arch Intern Med. 1966;117:206–212.
2. 3) Vasen HF, Mecklin JP, Khan PM, Lynch HT. The International Collaborative Group on Hereditary Non-Polyposis Colorectal Cancer (ICG-HNPCC). Dis Colon Rectum. 1991;34:424–425.
3. 4) Vasen HF. Clinical diagnosis and management of hereditary colorectal cancer syndromes. J Clin Oncol. 2000;18:81S–92S.
4. 5) Umar A, Boland CR, Terdiman JP, Syngal S, de la Chapelle A, Rüschoff J, et al. Revised Bethesda Guidelines for hereditary nonpolyposis colorectal cancer (Lynch syndrome) and microsatellite instability. J Natl Cancer Inst. 2004;96:261–268.
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