Recent Advances and Current Management for Desmoid Tumor Associated with Familial Adenomatous Polyposis
Author:
Affiliation:
1. Department of Gastroenterological Surgery, Kagawa University
2. Department of Digestive Tract and General Surgery, Saitama Medical Center, Saitama Medical University
3. Cancer Treatment Center, Toyonaka Municipal Hospital
Publisher
The Japan Society of Coloproctology
Subject
General Medicine
Link
https://www.jstage.jst.go.jp/article/jarc/7/2/7_2022-074/_pdf
Reference106 articles.
1. 1. Arvanitis ML, Jagelman DG, Fazio VW, et al. Mortality in patients with familial adenomatous polyposis. Dis Colon Rectum. 1990 Aug; 33 (8): 639-42.
2. 2. Bertario L, Presciuttini S, Sala P, et al. Causes of death and postsurgical survival in familial adenomatous polyposis: results from the Italian Registry. Italian Registry of Familial Polyposis Writing Committee. Semin Surg Oncol. 1994 May-Jun; 10 (3): 225-34.
3. 3. Fletcher CDM BJ, Hogendoorn PCW, Mertens F, editor. WHO Classification of tumours of soft tissue and bone. Pathology and genetics of tumours of soft tissue and bone. 4th ed. Lyon: IARC Press; 2013.
4. 4. Nieuwenhuis MH, Casparie M, Mathus-Vliegen LM, et al. A nation-wide study comparing sporadic and familial adenomatous polyposis-related desmoid-type fibromatoses. Int J Cancer. 2011 Jul; 129 (1): 256-61.
5. 5. Koskenvuo L, Ristimäki A, Lepistö A. Comparison of sporadic and FAP-associated desmoid-type fibromatoses. J Surg Oncol. 2017 Nov; 116 (6): 716-21.
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