Literature DB >> 1318618

Spectrum of clinical manifestations of familial adenomatous polyposis.

A K Sohrabi1, P Nowzari.   

Abstract

Familial adenomatous polyposis is an autosomal dominant disease that primarily involves the colon, but may involve other organs such as the central nervous system, ampulla of Vater, liver, soft tissue and the remainder of the gastrointestinal tract. In this report we present the adenocarcinoma of the uterus and adenocarcinoma of the ovary as a new addition to the clinical spectrum of familial adenomatous polyposis. Due to the tendency for development of multiple primary carcinomas in patients with familial adenomatous polyposis, these patients need to be followed very closely for detection of new malignancies. If diagnosed early and treated accordingly, they could have a long-term postoperative survival.

Entities:  

Mesh:

Year:  1992        PMID: 1318618

Source DB:  PubMed          Journal:  W V Med J        ISSN: 0043-3284


  1 in total

1.  Pancreatic islet cell tumour in a patient with familial adenomatous polyposis.

Authors:  C J Stewart; C W Imrie; A K Foulis
Journal:  J Clin Pathol       Date:  1994-09       Impact factor: 3.411

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.