Literature DB >> 21536347

[Familial adenomatous polyposis and liver metastases from a neuroendocrine tumor].

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.
Copyright © 2010 Elsevier España, S.L. All rights reserved.

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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


  1 in total

1.  Primary high-grade neuroendocrine carcinoma emerging from an adenomatous polyp in the setting of familial adenomatous polyposis.

Authors:  Claire J Detweiler; Diana M Cardona; David S Hsu; Shannon J McCall
Journal:  BMJ Case Rep       Date:  2016-02-16
  1 in total

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