Review article: The non-inherited gastrointestinal polyposis syndromes

E. M. Ward, H. C. Wolfsen

Research output: Contribution to journalReview articlepeer-review

67 Scopus citations

Abstract

The non-inherited gastrointestinal polyposis syndromes represent a group of rare disorders characterized by the presence of multiple, non-adenomatous polyps on the gastrointestinal mucosa occurring in unrelated patients. We present here a review of the clinical and histopathological aspects of the syndromes to include the Cronkhite-Canada syndrome, hyperplastic polyposis and lipomatous polyposis. While infrequently encountered, these diseases can have devastating clinical effects that may be aggravated by delays in diagnosis and treatment. Prompt accurate diagnosis and treatment of these uncommon disorders depend on a sound working knowledge of the distinct clinical and pathological features described herein.

Original languageEnglish (US)
Pages (from-to)333-342
Number of pages10
JournalAlimentary Pharmacology and Therapeutics
Volume16
Issue number3
DOIs
StatePublished - Mar 21 2002

ASJC Scopus subject areas

  • Hepatology
  • Gastroenterology
  • Pharmacology (medical)

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