H. Matsubayashi et al., Different amounts of K-ras mutant epithelial cells in pancreatic carcinomaand mass-forming pancreatitis, PANCREAS, 21(1), 2000, pp. 77-85
Clinically, differential diagnosis of pancreatic carcinoma (PC) and so-call
ed "mass-forming pancreatitis (MFP)" is difficult. We analyzed the amount,
ductal level, and K-ras mutation of ductal hyperplasia and intraductal carc
inoma in surgically resected cases of MFP (n = 18) and PC (n = 16). DNAs ex
tracted from microdissected epithelial foci were analyzed for K-ras codon 1
2 mutation by nested polymerase chain reaction and restriction fragment len
gth polymorphism. The histology of MFP showed severe destruction of exocrin
e tissue and pancreatic stones and/or protein plugs (72%, 13 of 18 cases) i
n mostly peripheral ducts. The average basal membrane lengths of nonpapilla
ry and papillary hyperplasia in cases of carcinoma were about 4 and 15 time
s more than those of MFP, respectively. The frequency of K-ras mutation in
hyperplastic foci increased from nonpapillary [six (27%) of 22] to papillar
y foci [16 (64%) of 25] in K-ras mutant PCs, but there was no difference be
tween nonpapillary [one (6%) of 18] and papillary foci (none of 19) in K-ra
s wild-type PCs, and also between nonpapillary (none of 24) and papillary f
oci [one (7%) of 14] in MFPs.