Citation
Y. Sakai et al., Origin of giant cells in osteoclast-like giant cell tumors of the pancreas, HUMAN PATH, 31(10), 2000, pp. 1223-1229
Abstract
To clarify the origin of giant cells in osteoclast-like giant cell tumors (
OGCTs) of the pancreas, we performed microscopical, inmunohistochemical, an
d K-ras gene mutation analyses with a microdissection approach in 3 cases,
featuring 4 cellular components (osteoclast-like giant cells [OGCs], pleomo
rphic large cells [PLCs], mononuclear cells, and ductal carcinoma cells). T
wo cases had abundant OGCs, and 1 case contained large number of both OGCs
and PLCs. In each, none of the microdissected OGCs contained any K-ras gene
mutation while they were positive for a histiocytic marker (CD-68). In con
trast, PLCs, when present, frequently harbored K-ras gene mutations and wer
e negative for CD-68. In all cases, mononuclear cells, a mixture of histioc
yte-like and atypical, from microscopic and immunohistochemical viewpoints,
also frequently showed K-ras alteration. Histiocyte-like mononuclear cell
was equipped with a regular and oval nucleus similar to those in OGCs and w
as positive for CD-68. Atypical mononuclear cell showed an irregular, pleom
orphic, or sometimes bizarre nucleus similar to those in PLCs and was negat
ive for CD-68. All of the K-ras gene mutations found in PLCs and mononuclea
r cells were the same as in the ductal carcinoma cells within the same tumo
r. Thus, OGCs differ in origin from ductal cells and are strongly suggested
to be nonneoplastic and of mesenchymal origin, whereas PLCs, which harbor
K-ras gene mutations, are neoplastic and presumably derived from ductal car
cinoma cells. Moreover, mononuclear cells may be classified into 2 types, h
istiocyte-like and atypical. HUM PATHOL 31:1223-1229. Copyright (C) 2000 by
W.B. Saunders Company.