Literature DB >> 30117372

Update on small bowel surveillance in hereditary colorectal cancer syndromes.

Lupe Sanchez-Mete1, Vittoria Stigliano1.   

Abstract

Despite its rarity in the general population, small bowel adenocarcinoma risk is increased in individuals with hereditary colorectal cancer syndromes (HCCS). In the last decade, the advent of capsule endoscopy and device-assisted balloon enteroscopy procedures in patients with HCCS have allowed to investigate the whole small bowel, increasing the diagnostic yield of small bowel tumor. Nonetheless, there is a significant variability in the international guideline recommendations. The aim of this review is to provide an update on surveillance of small bowel in HCCS and to identify the key points for the clinical management of these patients.

Entities:  

Keywords:  Hereditary colorectal cancer syndromes; Lynch syndrome; Peutz-Jeghers syndrome; familial polyposis; small bowel cancer; surveillance

Mesh:

Year:  2018        PMID: 30117372     DOI: 10.1177/0300891618792461

Source DB:  PubMed          Journal:  Tumori        ISSN: 0300-8916            Impact factor:   2.098


  1 in total

1.  Ovarian metastases from ileum cancer in a patient with germline EPCAM gene deletion successfully treated with surgical resection and CAPOX chemotherapy: a case report.

Authors:  Narushi Iwata; Ayumi Shikama; Wataru Takao; Yoshihiko Hosokawa; Hiroya Itagaki; Nobutaka Tasaka; Azusa Akiyama; Hiroyuki Ochi; Takeo Minaguchi; Miwa Arita; Emiko Noguchi; Toshikazu Moriwaki; Toyomi Satoh
Journal:  BMC Med Genet       Date:  2020-04-09       Impact factor: 2.103

  1 in total

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