| Literature DB >> 16437731 |
Vito D Corleto1, Ermira Zykaj, Paolo Mercantini, Emanuela Pilozzi, Michele Rossi, Antonella Carnuccio, Emilio Di Giulio, Vincenzo Ziparo, Gianfranco Delle Fave.
Abstract
A 34-year-old male with hereditary non-polyposis colon cancer with a mutation in hMSH2 line is reported. Despite regular colonoscopic follow-up, he developed cecal cancer involving the extraluminal area. Due to sub-occlusive symptoms, the patient was submitted to further colonoscopy, however with no clear evidence of neoplasia. Thin slice multiplanar reconstruction computed tomography CT scan performed thereafter revealed a transmural mass 2.5 cm in size localized near the cecal valve. Discussion is made on the reliability of colonoscopic examinations as well as the need for further investigations in the follow-up of patients at very high risk of right-sided colon cancer, such as male hMSH2 carrier affected by hereditary non-polyposis colon cancer.Entities:
Mesh:
Year: 2005 PMID: 16437731 PMCID: PMC4725167 DOI: 10.3748/wjg.v11.i47.7541
Source DB: PubMed Journal: World J Gastroenterol ISSN: 1007-9327 Impact factor: 5.742