In hereditary non-polyposis colorectal cancer (HNPCC) patients, the ca
ncer frequently arises in the proximal colon and is often multiple (sy
nchronous or metachronous). Pathologic differences seem to exist betwe
en hereditary and sporadic Barge bowel cancer, but the data are not un
iform. Many authors reported that the following histologic features ar
e often present in HNPCC: 1) mucinous histotype, 2) poorly differentia
ted tumors, 3) presence of peritumoral lymphocytic infiltrate, with Cr
ohn's-like lymphoid reaction. Such features have also been found in ap
parently sporadic colorectal cancer with, but not in sporadic colorect
al cancer without DNA replication errors. Many studies have suggested
that adenoma plays a main role in HNPCC carcinogenesis, and that the '
'adenoma-carcinoma sequence'' may be the pathway to cancer in HNPCC as
in sporadic colorectal cancer. Moreover, HNPCC adenomas show an early
onset, villous component, high-grade dysplasia, and positivity for DN
A replication errors more frequently than sporadic adenomas. Such data
suggest that the adenoma-carcinoma sequence is accelerated in HNPCC a
nd that surveillance in these patients should therefore be strict to a
void cancer development.