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References

  • 1
    FletcherCDM, UnniKK, MertensF, eds. World Health Organization Classification of Tumours. Pathology and genetics of tumours of soft tissue and bone. Lyon: IARC Press, 2002.
  • 2
    Nieuwenhuis MH, De Vos Tot Nederveen Cappel W, Botma A, Nagengast FM, Kleibeuker JH, Mathus-Vliegen EM, Dekker E, Dees J, Wijnen J, Vasen HF. Desmoid tumors in a dutch cohort of patients with familial adenomatous polyposis. Clin Gastroenterol Hepatol 2008; 6: 2159.
  • 3
    Lefevre JH, Parc Y, Kernéis S, Goasguen N, Benis M, Parc R, Tiret E. Risk factors for development of desmoid tumours in familial adenomatous polyposis. Br J Surg 2008; 95: 11369.
  • 4
    Sturt NJH, Clark SK. Current ideas in desmoid tumours. Fam Cancer 2006; 5: 27585.
  • 5
    Rampone B, Pedrazzani C, Marrelli D, Pinto E, Roviello F. Updates on abdominal desmoid tumors. World J Gastroenterol 2007; 13: 598588.
  • 6
    Reitamo J, Scheinin T, Hayry P. The desmoid syndrome. New aspects in the cause, pathogenesis and treatment of the desmoid tumor. Am J Surg 1986; 151: 2307.
  • 7
    Groen EJ, Roos A, Muntinghe FL, Enting RH, de Vries J, Kleibeuker JH, Witjes MJ, Links TP, van Beek AP. Extra-intestinal manifestations of familial adenomatous polyposis. Ann Surg Oncol 2008; 15: 243950.
  • 8
    Shields CJ, Winter DC, Kirwan WO, Redmond HP. Desmoid tumours. Eur J Surg Oncol 2001; 27: 7016.
  • 9
    Gurbuz AK, Giardiello FM, Petersen GM, Krush AJ, Offerhaus GJ, Booker SV, Kerr MC, Hamilton SR. Desmoid tumours in familial adenomatous polyposis. Gut 1994; 35: 37781.
  • 10
    Bertario L, Russo A, Sala P, Eboli M, Giarola M, D'amico F, Gismondi V, Varesco L, Pierotti MA, Radice P. Hereditary colorectal tumours registry. Genotype and phenotype factors as determinants of desmoid tumors in patients with familial adenomatous polyposis. Int J Cancer 2001; 95: 1027.
  • 11
    Fallen T, Wilson M, Morlan B, Lindor NM. Desmoid tumors-a characterization of patients seen at Mayo Clinic 1976–1999. Fam Cancer 2006; 5: 19194.
  • 12
    Lips DJ, Barker N, Clevers H, Hennipman A. The role of APC and beta-catenin in the aetiology of aggressive fibromatoses (desmoid tumors). Eur J Surg Oncol 2009; 35: 310.
  • 13
    Bussey HJR. Familial polyposis coli. Baltimore: John Hopkins University Press, 1975.
  • 14
    Casparie M, Tiebosch ATMG, Burger G, Blauwgeers H, Pol A, van de Krieken JHJM, van Meijer GA. Pathology databanking and biobanking in The Netherlands, a central role for PALGA, the nationwide histiopathology and cytopathology data network and archive. Cell Oncol 2007; 29: 1924.
  • 15
    Cote RA, Robboy S. Progress in medical information management. Systematized nomenclature of medicine (SNOMED). JAMA 1980; 22: 75662.
  • 16
    Goettsch WG, Bos SD, Breekveldt-Postma N, Casparie M, Herings RMC, Hogendoorn PCW. Incidence of gastrointestinal stromal tumours is underestimated: results of a nation-wide study. Eur J Cancer 2005; 41: 286872.
  • 17
    Odink AE, van Asperen CJ, Vandenbroucke JP, Cleton-Jansen AM, Hogendoorn PCW. An association between cartilaginous tumours and breast cancer in the national pathology registration in The Netherlands points towards a possible genetic trait. J Pathol 2001; 193: 19092.
  • 18
    Bisgaard ML, Fenger K, Bülow S, Niebuhr E, Mohr J. Familial adenomatous polyposis (FAP): frequency, penetrance, and mutation rate. Hum Mut 1994; 3: 1215.
  • 19
    Dekkers OM, von Elm E, Algra A, Romijn JA, Vandenbroucke JP. How to assess the external validity of therapeutic trials: a conceptional approach. Int J Epidemiol 2010; 39: 8994.
  • 20
    Giarola M, Wells D, Mondini P, Pilotti S, Sala P, Azzarelli A, Bertario L, Pierotti MA, Delhanty JD, Radice P. Mutations of adenomatous polyposis coli (APC) gene are uncommon in sporadic desmoid tumours. Br J Cancer 1998; 78: 5827.
  • 21
    Brueckl WM, Ballhausen WG, Förtsch T, Günther K, Fiedler W, Gentner B, Croner R, Boxberger F, Kirchner T, Hahn EG, Hohenberger W, Wein A. Genetic testing for germline mutations of the APC gene in patients with apparently sporadic desmoid tumors but a family history of colorectal carcinoma. Dis Colon Rectum 2005; 48: 127581.
  • 22
    Bandipalliam P, Balmana J, Syngal S. Comprehensive genetic and endoscopic evaluation may be necessary to distinguish sporadic versus familial adenomatous polyposis-associated abdominal desmoid tumors. Surgery 2004; 135: 6839.
  • 23
    Benoit L, Faivre L, Cheynel N, Ortega-Deballon P, Facy O, Marty M, Olschwang S, Fraisse J, Cuisenier J. 3′ Mutation of the APC gene and family history of FAP in a patient with apparently sporadic desmoid tumors. J Clin Gastroenterol 2007; 41: 297300.
  • 24
    Eccles D, Harvey J, Bateman A, Ross F. A novel 3′ mutation in the APC gene in a family presenting with a desmoid tumour. J Med Genet 2001; 38: 8613.