| Literature DB >> 21536347 |
Concepción Grau García1, Asunción Soto Gutierrez, Encarnación Andrada Becerra, Beatriz Sánchez Heras, Beatriz Sánchez De las Heras, Javier Gallego Plazas, Alicia Brotons Brotons, Javier Sola-Vera Sánchez, María Dolores Picó Sala.
Abstract
Familial adenomatous polyposis (FAP) is mainly characterized by the development of a large number of polyps in the gastrointestinal tract and by the risk of developing adenocarcinomas. We present the case of a woman diagnosed with FAP and liver metastases. Histological analysis revealed both diseases to be secondary to a neuroendocrine tumor. To date, only three cases showing the simultaneous occurrence of these two entities have been published. Currently, there is no genetic basis to explain the coexistence of these two diseases, both of which have a very low prevalence.Entities:
Mesh:
Year: 2011 PMID: 21536347 DOI: 10.1016/j.gastrohep.2011.02.007
Source DB: PubMed Journal: Gastroenterol Hepatol ISSN: 0210-5705 Impact factor: 2.102