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Inicio Gastroenterología y Hepatología Avances en la etiopatogenia, identificación y manejo clínico de las formas her...
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Vol. 34. Issue S1.
Jornada de Actualización en Gastroenterología Aplicada
Pages 70-75 (January 2011)
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Vol. 34. Issue S1.
Jornada de Actualización en Gastroenterología Aplicada
Pages 70-75 (January 2011)
Oncología digestiva
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Avances en la etiopatogenia, identificación y manejo clínico de las formas hereditarias y familiares de cáncer colorrectal
Advances in the etiopathogenesis, identification and clinical management of hereditary and familial colorectal cancer
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2944
María Dolores Giráldez
Servei de Gastroenterologia, Institut de Malalties Digestives i Metabòliques, Hospital Clínic, CIBERehd, IDIBAPS, Universidad de Barcelona, Barcelona, España
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Resumen

Las formas hereditarias y familiares de cáncer colorrectal (CCR) representan aproximadamente un 30–35% de los casos de CCR. Su identificación y el correcto manejo de estas familias son fundamentales, ya que constituyen un grupo de alto riesgo de CCR que se beneficia de medidas preventivas específicas para evitar el desarrollo de esta neoplasia. Además, en algunas de estas formas de CCR, principalmente en el CCR familiar, las alteraciones responsables de la susceptibilidad genética no están bien caracterizadas, lo cual resulta prioritario para su adecuado diagnóstico y manejo. En esta revisión se discuten las novedades más importantes, presentadas en el congreso de la American Gastroenterological Association, en cuanto a etiopatogenia, identificación y manejo clínico de las formas hereditarias y familiares de CCR.

Palabras clave:
Cáncer colorrectal ereditario
Síndrome de Lynch
Poliposis adenomatosa familiar
Poliposis hiperplásica
Síndrome de Peutz-Jeghers
Abstract

Hereditary and familial forms of colorectal cancer (CRC) represent approximately 30–35% of CRC cases. Identification of these forms and appropriate management of affected families are essential, as they constitute a group at high risk of CRC that benefits from specific preventive measures. Moreover, in some of these forms of CRC, mainly familial CRC, the alterations causing genetic susceptibility are not well characterized and thus identification of these alterations is a priority for correct diagnosis and management. The present review discusses the most important advances presented at the American Gastroenterological Association's congress on the etiopathogenesis, identification and clinical management of hereditary and familial CRC.

Keywords:
Hereditary colorectal cancer
Lynch syndrome
Familial adenomatous polyposis
Hyperplastic polyposis syndrome
Peutz-Jeghers syndrome
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Bibliografía
[1.]
V. Piñol, M. Andreu, A. Castells, A. Payá, X. Bessa, R. Jover.
Frequency of hereditary nonpolyposis colorectal cancer and other colorectal cancer familial forms in Spain.
Eur J Gastroenterol Hepatol, 16 (2004), pp. 39-45
[2.]
K.W. Jasperson, T.M. Tuohy, D.W. Neklason, R.W. Burt.
Hereditary and familial colon cancer.
Gastroenterology, 138 (2010), pp. 2044-2058
[3.]
H. Hampel, W.L. Frankel, E. Martin, M. Arnold, K. Khanduja, P. Kuebler, et al.
Feasibility of screening for Lynch syndrome among patients with colorectal cancer.
J Clin Oncol, 26 (2008), pp. 5783-5788
[4.]
L. Pérez-Carbonell, C. Ruiz-Ponte, X. Bessa, J.L. Soto, A. Castillejo, V. Barberá, et al.
Comparison between routine immunohistochemistry for mismatch repair proteins versus revised Bethesda guidelines in the diagnosis of Lynch syndrome in a non-selected population of colorectal cancer patients.
Gastroenterology, 138 (2010), pp. S297
[5.]
M.S. Pino, M. Mino-Kenudson, B.M. Wildemore, A. Ganguly, J. Batten, I. Sperduti, et al.
Deficient DNA mismatch repair is common in Lynch syndrome-associated colorectal adenomas.
J Mol Diagn, 11 (2009), pp. 238-247
[6.]
C.H. Leenen, M.G. Van Lier, A. Wagner, W. Dinjens, E.J. Dubbink, M.E. Van Leerdam, et al.
Routine MSI-analysis in advanced adenomas in patients younger than 45 years leads to the identification of more patients at high risk for Lynch syndrome.
Gastroenterology, 138 (2010), pp. S294
[7.]
R.A. Barnetson, A. Tenesa, S.M. Farrington, I.D. Nicholl, R. Cetnarskyj, M.E. Porteous, et al.
Identification and survival of carriers of mutations in DNA mismatch-repair genes in colon cancer.
N Engl J Med, 354 (2006), pp. 2751-2763
[8.]
S. Chen, W. Wang, S. Lee, K. Nafa, J. Lee, K. Romans, et al.
Prediction of germline mutations and cancer risk in the Lynch syndrome.
JAMA, 296 (2006), pp. 1479-1487
[9.]
J. Balmaña, D.H. Stockwell, E.W. Steyerberg, E.M. Stoffel, A.M. Deffenbaugh, J.E. Reid, et al.
Prediction of MLH1 and MSH2 mutations in Lynch syndrome.
JAMA, 296 (2006), pp. 1469-1478
[10.]
F. Kastrinos, E.W. Steyerberg, J. Balmaña, R. Mercado, S. Gallinger, R.W. Haile, et al.
Comparison of the clinical prediction model Premm1,2,6 with colorectal cancer molecular tumor testing for Lynch syndrome in the Colon Cancer Family Registry.
Gastroenterology, 138 (2010), pp. S149-S150
[11.]
O. Khan, A. Blanco, P. Conrad, C. Gulden, S. Kupfer, J.P. Terdiman.
Validation of Lynch syndrome predictive models in a multi-center United States referral cohort.
Gastroenterology, 138 (2010), pp. S150
[12.]
J.P. Terdiman, T.R. Levin, B.A. Allen, J.R. Gum Jr, A. Fishbach, P.G. Conrad, et al.
Hereditary nonpolyposis colorectal cancer in young colorectal cancer patients: high-risk clinic versus populationbased registry.
Gastroenterology, 122 (2002), pp. 940-947
[13.]
S.M. Farrington, A. Tenesa, R. Barnetson, A. Wiltshire, J. Prendergast, M. Porteous, et al.
Germline susceptibility to colorectal cancer due to base-excision repair gene defects.
Am J Hum Genet, 77 (2005), pp. 112-119
[14.]
M.D. Giráldez, F. Balaguer, M. Cuatrecasas, J. Muñoz, V. Alonso-Espinaco, L. Bujanda, et al.
High frequency of msh6 germline mutations in early-onset colorectal cancer.
Gastroenterology, 138 (2010), pp. S150
[15.]
S. Masciari, V.A. Joshi, R. Mercado, J.L. Walsh, N.M. Lindor, S. Gallinger, et al.
Prevalence of germline TP53 mutations in 510 population and clinic-based cases of colorectal cancer diagnosed under age 40.
Gastroenterology, 138 (2010), pp. S150-S151
[16.]
N. Al-Tassan, N.H. Chmiel, J. Maynard, N. Fleming, A.L. Livingston, G.T. Williams, et al.
Inherited variants of MYH associated with somatic G:C→T: a mutations in colorectal tumors.
Nat Genet, 30 (2002), pp. 227-232
[17.]
S. Grover, A. Dewanwala, S. Syngal.
Phenotypic differences between APC and biallelic MUTYH mutation carriers in 1,193 individuals with attenuated polyposis.
Gastroenterology, 138 (2010), pp. S294
[18.]
K.S. Boparai, J.B. Reitsma, V. Lemmens, T.A. Van Os, E. Mathus-Vliegen, J.J. Koornstra, et al.
First-degree relatives of hyperplastic polyposis patients have an increased colorectal cancer risk.
Gastroenterology, 138 (2010), pp. S102-S103
[19.]
M.G. Van Lier, E. Mathus-Vliegen, A. Wagner, M.E. Van Leerdam, E.J. Kuipers.
High intussusception risk at young age in patients with Peutz-Jeghers syndrome: time to update surveillance guidelines?.
Gastroenterology, 138 (2010), pp. S138
[20.]
M.G. Van Lier, A.M. Westerman, A. Wagner, C.W. Looman, J.H. Wilson, F.W. De Rooij, et al.
High cumulative and relative cancer risk and increased mortality in patients with Peutz-Jeghers syndrome.
Gastroenterology, 138 (2010), pp. S296
[21.]
K. Hemminki, B. Chen.
Familial risk for colorectal cancers are mainly due to heritable causes.
Cancer Epidemiol Biomarkers Prev, 13 (2004), pp. 1253-1256
[22.]
A. Abulí, C. Fernández-Rozadilla, V. Alonso-Espinaco, M.D. Giráldez, J. Muñoz, X. Bessa, et al.
S1984. Case-control genetic association study of candidates genes for genetic susceptibility to colorectal cancer.
Gastroenterology, 138 (2010), pp. 295
[23.]
I.W. Saunders, F.A. Macrae, G.P. Young, I. Blanco, J.P. Ross, J. Brohede, et al.
Evidence for a new susceptibility region on chromosome 9 from a genome-wide linkage study in non-syndromic colorectal cancer families.
Gastroenterology, 138 (2010), pp. S295
Copyright © 2011. Elsevier España S.L.. Todos los derechos reservados
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