Gastrointestinal polyposis syndromes

M. C. Finan, M. K. Ray

Research output: Contribution to journalReview articlepeer-review

43 Scopus citations

Abstract

A number of interesting syndromes are now recognized in which gastrointestinal polyps and characteristic cutaneous findings coexist. Gardner's syndrome (familial adenomatous polyposis) and Peutz-Jeghers syndrome, both autosomal dominant genodermatoses, are perhaps best known. Cronkhite-Canada syndrome is a rare acquired disease of adulthood in which gastrointestinal polyps and skin findings also define the syndrome. Colonic polyps are a variable finding in Cowden's disease. Muir-Torre syndrome, and neurofibromatosis. Nonetheless, recognition of the cutaneous lesions that accompany and sometimes precede the intestinal symptoms in these various syndromes may potentially hasten early, accurate diagnosis and aid in prevention of potentially life-threatening complications. Lastly, a newly described syndrome - the Ruvalcabe-Myhre-Smythe syndrome - is introduced, and the controversial topic of acrochordons and their relation to colonic polyps is discussed.

Original languageEnglish (US)
Pages (from-to)419-434
Number of pages16
JournalDermatologic Clinics
Volume7
Issue number3
DOIs
StatePublished - 1989
Externally publishedYes

ASJC Scopus subject areas

  • Dermatology

Fingerprint Dive into the research topics of 'Gastrointestinal polyposis syndromes'. Together they form a unique fingerprint.

Cite this