2009
DOI: 10.1111/j.1365-2559.2008.03192.x
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Gallbladder cancer: a morphological and molecular update

Abstract: Gallbladder cancer (GBC) shows a marked geographical variation in its incidence, with the highest figures being seen in India and Chile and relatively low levels in many Western countries. Risk factors for its development include the presence of gallstones, infection and the presence of an anomalous pancreatobiliary ductal junction. It can arise from either a pathway involving metaplasia or dysplasia or one in which there is a pre-existing adenoma. The former is the more common and, because it is often not ass… Show more

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Cited by 177 publications
(117 citation statements)
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“…1,15,19,22,24 In the western hemisphere, very few groups are interested in reproducing this experience. So far, only Hemming et al 15 published a consisted report with HPD in the western countries.…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…1,15,19,22,24 In the western hemisphere, very few groups are interested in reproducing this experience. So far, only Hemming et al 15 published a consisted report with HPD in the western countries.…”
Section: Discussionmentioning
confidence: 99%
“…22 Thus, due to the rich submucosal network of the infundibulum region, the tumors of this region are generally more aggressive, frequently present with advanced lymph node disease, hepatoduodenal ligament involvement and may mimic a hilar PseudoKlatskin cholangiocarcinoma. Tumors at the bottom of the gallbladder are more likely to be resected and their treatment should invariably comprise hepatic resection.…”
Section: -21mentioning
confidence: 99%
“…The two main morphological pathways to gallbladder carcinoma are through metaplasia and dysplasia in flat mucosa (the more common scenario), or arising within a macroscopically visible adenoma. There are certain differences at a molecular level between the pathways [6].…”
Section: Discussionmentioning
confidence: 99%
“…Only few somatic genetic changes including mutations in K-ras, TP53 and p16 Ink4 /CDKN2 as well as loss of heterozygosity at several chromosomal regions harboring known or putative tumor-suppressor genes have been reported in GCs. 5,7 Hence, identification of novel genetic factors associated with susceptibility to GC should provide new insights into pathogenesis and novel therapeutic interventions of GC. Here, we report a genome-wide association study (GWAS) that aims to identify genetic factors associated with GC susceptibility.…”
Section: Introductionmentioning
confidence: 99%
“…Only few somatic genetic changes including mutations in K-ras, TP53 and p16 Ink4 /CDKN2 as well as loss of heterozygosity at several chromosomal regions harboring known or putative tumor-suppressor genes have been reported in GCs. 5,7 Hence, identification of novel genetic factors associated with susceptibility to GC should …”
mentioning
confidence: 99%