Article
Multiple desmoid tumors in a patient with familial adenomatous polyposis caused by the novel W421X mutation.
Revista espanola de enfermedades digestivas - 1 Mar 2012
Ioannidis Orestis, Paraskevas George, Chatzopoulos Stavros, Kotronis Anastasios, Papadimitriou Nikolaos, Konstantara Athina, Makrantonakis Apostolos, Kakoutis Emmanouil
Abstract excerpt
Familial adenomatous polyposis (FAP) is a rare syndrome characterized by the presence of hundreds to thousands of colorectal adenomas and is responsible for less than 1% of all colorectal cancers. The syndrome is also characterized by extra-colorectal features including amongst others upper gastrointestinal tract polyps and desmoid tumors. The syndrome is inherited by an autosomal dominant gene, the adenomatous...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.
