Literature DB >> 11689361

Polyposis syndromes: pediatric implications.

W Hyer1.   

Abstract

The diagnosis of a polyposis syndrome, such as juvenile polyposis, Peutz-Jeghers syndrome, and familial adenomatous polyposis, requires knowledge of the site, number, and histologic type of the polyps and an appreciation of relevant family history. Children and adolescents with polyposis syndromes are faced with not only the immediate complications of the polyps, such as intussusception or bleeding, but also the extraintestinal manifestations and the long-term risk for malignancy. This article reviews the diagnosis, clinical management, surveillance, and surgical options for children with polyposis syndromes and discusses genetics and appropriate screening programs.

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Mesh:

Year:  2001        PMID: 11689361

Source DB:  PubMed          Journal:  Gastrointest Endosc Clin N Am        ISSN: 1052-5157


  1 in total

1.  A web-based assessment of pediatrics resident medical knowledge in childhood hereditary gastrointestinal cancer predisposing syndromes.

Authors:  Julie Stoner; Yongyue Qi; Steven H Erdman; Thomas M Attard
Journal:  J Cancer Educ       Date:  2009       Impact factor: 2.037

  1 in total

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