Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/18638
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dc.contributor.authorBeggs, A. D.cat
dc.contributor.authorLatchford, A. R.cat
dc.contributor.authorVasen, Hans F. A.cat
dc.contributor.authorMöslein, Gabrielacat
dc.contributor.authorAlonso, A.cat
dc.contributor.authorAretz, S.cat
dc.contributor.authorBertario, Luciocat
dc.contributor.authorBlanco Guillermo, Ignaciocat
dc.contributor.authorBülow, S.cat
dc.contributor.authorBurn, Johncat
dc.contributor.authorCapellá, G. (Gabriel)cat
dc.contributor.authorColas, Chrystellecat
dc.contributor.authorFriedl, W.cat
dc.contributor.authorMøller, Pålcat
dc.contributor.authorHes, F. J.cat
dc.contributor.authorJärvinen, Heikkicat
dc.contributor.authorMecklin, Jukka-Pekkacat
dc.contributor.authorNagengast, F. M.cat
dc.contributor.authorParc, Yanncat
dc.contributor.authorPhillips, R. K. S.cat
dc.contributor.authorHyer, W.cat
dc.contributor.authorPonz de Leon, Mauriziocat
dc.contributor.authorRenkonen-Sinisalo, Lauracat
dc.contributor.authorSampson, J. R.cat
dc.contributor.authorStormorken, A.cat
dc.contributor.authorTejpar, Sabinecat
dc.contributor.authorThomas, H. J. W.cat
dc.contributor.authorWijnen, Juulcat
dc.contributor.authorClark, Susan K.cat
dc.contributor.authorHodgson, Shirley V.cat
dc.date.accessioned2011-07-07T11:33:20Z-
dc.date.available2011-07-07T11:33:20Z-
dc.date.issued2010-
dc.identifier.issn0017-5749-
dc.identifier.urihttp://hdl.handle.net/2445/18638-
dc.description.abstractPeutz¿Jeghers syndrome (PJS, MIM175200) is an autosomal dominant condition defined by the development of characteristic polyps throughout the gastrointestinal tract and mucocutaneous pigmentation. The majority of patients that meet the clinical diagnostic criteria have a causative mutation in the STK11 gene, which is located at 19p13.3. The cancer risks in this condition are substantial, particularly for breast and gastrointestinal cancer, although ascertainment and publication bias may have led to overestimates in some publications. Current surveillance protocols are controversial and not evidence-based, due to the relative rarity of the condition. Initially, endoscopies are more likely to be done to detect polyps that may be a risk for future intussusception or obstruction rather than cancers, but surveillance for the various cancers for which these patients are susceptible is an important part of their later management. This review assesses the current literature on the clinical features and management of the condition, genotype¿phenotype studies, and suggested guidelines for surveillance and management of individuals with PJS. The proposed guidelines contained in this article have been produced as a consensus statement on behalf of a group of European experts who met in Mallorca in 2007 and who have produced guidelines on the clinical management of Lynch syndrome and familial adenomatous polyposis.eng
dc.format.extent12 p.-
dc.format.mimetypeapplication/pdf-
dc.language.isoengeng
dc.publisherBMJ Groupeng
dc.relation.isformatofReproducció digital del document publicat a: http://dx.doi.org/10.1136/gut.2009.198499cat
dc.relation.ispartofGut, 2010, vol. 59, núm. 7, p. 975-986-
dc.relation.urihttp://dx.doi.org/10.1136/gut.2009.198499-
dc.rights(c) BMJ Publishing Group Ltd and British Society of Gastroenterology, 2010-
dc.subject.classificationMalalties intestinalscat
dc.subject.classificationPòlips (Patologia)cat
dc.subject.otherIntestinal diseaseseng
dc.subject.otherPolyps (Pathology)eng
dc.titlePeutz-Jeghers syndrome: a systematic review and recommendations for managementeng
dc.typeinfo:eu-repo/semantics/article-
dc.typeinfo:eu-repo/semantics/publishedVersion-
dc.identifier.idgrec578379-
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess-
Appears in Collections:Articles publicats en revistes (Patologia i Terapèutica Experimental)

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