Colon polyps may be single or multiple, noninherited or inherited, his
tologically may vary from inflammatory, hamartomatous, neurogenic, or
adenomatous, and may be benign or malignant. The various recognized sy
ndromes are discussed including their clinical presentation, malignant
potential, and associated tumors. Recognition of these clinical syndr
omes will allow the clinician to categorize the patient and the relati
ve risk. The discussion goes into the genetic studies identifying the
adenomatous polyposis coli gene on chromosome 5 q21 and the identifica
tion of mutations arising in the DNA repair genes (MSA2, MLH1, PMSI, a
nd M52) in the HNPCC syndrome. This identified two divergent pathologi
es, both involving ''multiple hits'' with mucosal cells going from nor
mal to adenoma-dysplasia-carcinoma. The understanding of the multiple
hit concept with the adenoma-dysplasia-carcinoma progression will aid
in the further understanding of the broad neoplastic process. (C) 1997
Wiley-Liss, Inc.