Isolati, multipli, ereditari: Le tante facce dei polipi intestinali

Translated title of the contribution: Isolated, multiple, and hereditary intestinal polyps in children

Chiara Pierobon, Marta Flammini, Valentina Moressa, Stefano Martelossi, Alessandro Ventura

Research output: Contribution to journalArticle

Abstract

This article provides a critical review of the clinical presentation, pathology, genetics and management of the polyposis in childhood starting from the isolated juvenile polyp to the hereditary polyposis syndromes. These include the juvenile polyposis syndrome, Peutz-Jeghers syndrome, PTEN hamartoma tumor syndromes and familial adenomatous polyposis (FAP). These conditions typically outbreak in the second decade of life but early detection and proper screening and surveillance can minimize the risk of intestinal and extracolonic cancers. While juvenile polyp could be easily removed, the amartomatosis syndromes will require a specific endoscopic surveillance and a periodic polypectomy. In the case of FAP, the paediatrician has a decisive role in defining the colonscopic follow-up and the timing of the total colectomy.

Translated title of the contributionIsolated, multiple, and hereditary intestinal polyps in children
Original languageItalian
Pages (from-to)16-24
Number of pages9
JournalMedico e Bambino
Volume34
Issue number1
Publication statusPublished - Jan 1 2015

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health

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