A Duodenal Cancer Associated with Combined Syndrome of Juvenile Polyposis and Hereditary Hemorrhagic Telangiectasia
Author:
Affiliation:
1. Division of Hepato-biliary-pancreas Surgery, Department of Surgery, Faculty of Medicine, University of Miyazaki
2. Department of Surgery, Miyazaki Prefectural Miyazaki Hospital
Publisher
The Japanese Journal of Gastroenterological Surgery
Subject
Gastroenterology,Surgery
Link
https://www.jstage.jst.go.jp/article/jjgs/51/4/51_2017.0030/_pdf
Reference10 articles.
1. 1) Gallione CJ, Repetto GM, Legius E, Rustgi AK, Schelley SL, Tejpar S, et al. A combined syndrome of juvenile polyposis and hereditary hemorrhagic telangiectasia associated with mutations in MADH4 (SMAD4). Lancet. 2004 Mar;363(9412):852–859.
2. 2) Lin HC, Fiorino KN, Blick C, Anupindi SA. A rare presentation and diagnosis of juvenile polyposis syndrome and hereditary hemorrhagic telangiectasia overlap syndrome. Clin Imaging. 2015 Mar–Apr;39(2):321–324.
3. 3) Faughaman ME, Palda VA, Garcia-Tsao G, Geisthoff UW, Mcdonald J, Proctor DD, et al. International guidelines for the diagnosis and management of hereditary haemorrhagic telangiectasia. J Med Genet. 2011 Feb;48(2):73–87.
4. 5) Schumacher B, Frieling T, Borchard F, Hengeis KJ. Hereditary hemorrhagic telangiectasia associated with multiple pulmonary arteriovenous malformations and juvenile polyposis. Z Gastroenterol. 1994 Feb;32(2):105–108.
5. 6) Inoue S, Matsumoto T, Iida M, Hoshika K, Shimizu M, Hisamoto N, et al. Juvenile polyposis occurring in hereditary hemorrhagic telangiectasia. Am J Med Sci. 1999 Jan;317(1):59–62.
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