Succès et échecs du dépistage des formes familiales

作者: D. Bonnet , T. Babba , C. Hervé , T. Aparicio , R. Guimbaud

DOI: 10.1007/S11725-011-0316-3

关键词:

摘要: Le depistage des cancers colorectaux (CCR) lies au syndrome de Lynch (SL) repose sur l’identification criteres cliniques et biologiques. Il s’agit d’un processus en plusieurs etapes impliquant le clinicien, l’anatomopathologiste, biologiste finalement la consultation d’oncogenetique. Les resultats premieres experiences francaises mettent lumiere les difficultes realisation ce necessite motivation tous acteurs, l’explication enjeux patient disponibilite moyens d’organisation specifiques.

参考文章(40)
Ligue contre le cancer Comité de la Corrèze, Institut National du Cancer ,(2012)
Yves Bécouarn, Anne Rullier, Philippe Gorry, Denis Smith, Bruno Richard-Molard, Emmanuel Echinard, Patrick Texereau, Richard Beyssac, Jean-Louis Legoux, Hervé Lamouliatte, Thierry Frebourg, Sylviane Olschwang, Brigitte Gilbert, Laurence Venat, Véronique Picot, François Paraf, Michel Longy, Value of microsatellite instability typing in detecting hereditary non-polyposis colorectal cancer Gastroentérologie Clinique et Biologique. ,vol. 29, pp. 667- 675 ,(2005) , 10.1016/S0399-8320(05)82155-4
Wolfram Müller, Lawrence J. Burgart, Ruth Krause-Paulus, Stephen N. Thibodeau, M. Almeida, T. Brocker Edmonston, C. R. Boland, C. Sutter, J. R. Jass, A. Lindblom, J. Lubinski, K. MacDermot, D. S. A. Sanders, H. Morreau, A. Müller, C. Oliani, T. Orntoft, M. Ponz De Leon, C. Rosty, M. Rodriguez-Bigas, J. Rüschoff, A. Ruszkiewicz, J. Sabourin, R. Salovaara, Gabriela Möslein, The reliability of immunohistochemistry as a prescreening method for the diagnosis of hereditary nonpolyposis colorectal cancer (HNPCC)--results of an international collaborative study. Familial Cancer. ,vol. 1, pp. 87- 92 ,(2001) , 10.1023/A:1013840907881
H. F. A. VASEN, Review article: the Lynch syndrome (hereditary nonpolyposis colorectal cancer)* Alimentary Pharmacology & Therapeutics. ,vol. 26, pp. 113- 126 ,(2007) , 10.1111/J.1365-2036.2007.03479.X
Reijo Salovaara, Anu Loukola, Paula Kristo, Helena Kääriäinen, Heikki Ahtola, Matti Eskelinen, Niilo Härkönen, Risto Julkunen, Eero Kangas, Seppo Ojala, Jukka Tulikoura, Erkki Valkamo, Heikki Järvinen, Jukka-Pekka Mecklin, Lauri A. Aaltonen, Albert de la Chapelle, Population-Based Molecular Detection of Hereditary Nonpolyposis Colorectal Cancer Journal of Clinical Oncology. ,vol. 18, pp. 2193- 2200 ,(2000) , 10.1200/JCO.2000.18.11.2193
Stephan Jahn, Michael B. Minai-Pour, Michael R. Speicher, Angelika Reiner-Concin, Gerald Hoefler, Comprehensive screening for Lynch syndrome: who can be the driving force in daily clinical practice? Journal of Clinical Oncology. ,vol. 27, pp. 2292- 2292 ,(2009) , 10.1200/JCO.2009.22.0731
M G Dunlop, S M Farrington, I Nicholl, L Aaltonen, G Petersen, M Porteous, A Carothers, Population carrier frequency of hMSH2 and hMLH1 mutations British Journal of Cancer. ,vol. 83, pp. 1643- 1645 ,(2000) , 10.1054/BJOC.2000.1520
Catherine Julié, Christophe Trésallet, Antoine Brouquet, Céline Vallot, Ute Zimmermann, Emmanuel Mitry, François Radvanyi, Etienne Rouleau, Rosette Lidereau, Florence Coulet, Sylviane Olschwang, Thierry Frébourg, Philippe Rougier, Bernard Nordlinger, Pierre Laurent-Puig, Christophe Penna, Catherine Boileau, Brigitte Franc, Christine Muti, Hélène Hofmann-Radvanyi, Identification in daily practice of patients with Lynch syndrome (hereditary nonpolyposis colorectal cancer): revised Bethesda guidelines-based approach versus molecular screening. The American Journal of Gastroenterology. ,vol. 103, pp. 2825- 2835 ,(2008) , 10.1111/J.1572-0241.2008.02084.X
Ulrike Metzger, Anne Sophie Bats, Marie Aude Le Frère Belda, Sylviane Olschwang, Pierre Laurent Puig, Fabrice Lécuru, Cyrille Huchon, Contribution of ultrasonography to endometrial cancer screening in patients with hereditary nonpolyposis colorectal cancer/Lynch syndrome. International Journal of Gynecological Cancer. ,vol. 20, pp. 583- 587 ,(2010) , 10.1111/IGC.0B013E3181D7283A