A 68-yr-old woman was hospitalized because of abdominal pain, an enlar
ged pancreatic head by CT and a questionable 4-cm mass in the liver. F
ine-needle aspiration (FNA) of the pancreatic head disclosed a highly
cellular specimen consisting of clusters of cytologically bland, monot
onous, small nuclei and variable but generally sparse cytoplasm. Becau
se of the differentiated monomorphic character of the cell clusters, t
he postaspiration differential cytopathologic diagnosis included islet
cell tumor, acinic cell tumor, carcinoid, lymphoma, and well differen
tiated ductal adenocarcinoma. Pancreaticoduodenectomy and hepatic biop
sy yielded a grossly normal pancreas and a cirrhotic liver. Histologic
examination of the pancreas revealed a spotty but extensive spectrum
of islet changes ranging from normal to bland hyperplasia, nesidioblas
tosis, microadenosis, and neuroendocrine microadenomas, all appearing
in a light and electron microscopic context of an otherwise normal pan
creas. This case highlights the differential diagnostic ambiguities pr
esented by a continuum of pancreatic islet cell proliferations, especi
ally among patients in whom there are no known predisposing factors fo
r such diffuse preneoplastic or neoplastic changes. (C) 1993 Wiley-Lis
s, Inc.