Carcinoid tumors are potentially malignant neoplasms that arise in var
ious body sites, including the lung and gastrointestinal tract. Those
that appear cytologically atypical are more likely to behave aggressiv
ely than more typical carcinoid tumors. However, in the absence of cyt
ological atypia or large tumor size, it is difficult to predict the bi
ology of an individual tumor, because some lesions metastasize, wherea
s others do not. This study had four aims: (I) To study the expression
pattern of p53, Ki-67, NCAM, and S-100 in carcinoid tumors and to rel
ate these expression patterns to classical histopathologic features an
d to tumor location. (2) To identify nonhistological markers that migh
t more accurately predict the early behavior of carcinoid tumors. (3)
To determine whether sustentacular cells are present in carcinoid tumo
rs arising in tissues derived from different embryological derivatives
. (4) To determine the synaptophysin and chromogranin immunoreactivity
in neuroendocrine tumors arising in various locations. The immunostai
ning reactions were quantitatively scored by three observers. Only 3 o
f the 39 tumors (all histologically atypical) were strongly positive f
or Ki-67; two of these ic ere also strongly p53 immunoreactive. NCAM i
mmunostaining differed according to the site of origin: 76.5% of foreg
ut lesions, 58% of the midgut lesions, and 20% of hindgut lesions were
positive. S-100 immunostaining ranged from 41% in foregut lesions to
50% in both die hindgut- and midgut-derived tumors. S-100-positive sus
tentacular cells were present in 20.5% of carcinoid tumors. All tumors
stained with antibodies against synaptophysin. In contrast, 100% of m
idgut, 60% of hindgut, and 88% of foregut tumors were chromogranin pos
itive. Carcinoid tumors tend to have low proliferative rates. p53 immu
nostaining tends to be strongly positive in turners that are histologi
cally atypical, but it is negative in typical carcinoid tumors arising
in the gastrointestinal tract and lungs. Immunostaining reactions wit
h antibodies to NCAM, S-100, and chromogranin differ depending on the
site of origin. Synaptophysin stains 100% of carcinoid tumors regardle
ss of their site of origin. an contrast, antibodies to chromogranin fa
il to stain 40% of hindgut tumors and 12% of foregut carcinoid tumors.
S-100-positive sustentacular cells are present in foregut and midgut
tumors but not in hindgut tumors. Copyright (C) 1998 by W.B. Saunders
Company.