Jr. Riera et al., THE IMMUNOHISTOCHEMICAL DIAGNOSTIC PANEL FOR EPITHELIAL MESOTHELIOMA - A REEVALUATION AFTER HEAT-INDUCED EPITOPE RETRIEVAL, The American journal of surgical pathology, 21(12), 1997, pp. 1409-1419
The immunohistochemical diagnosis between epithelial mesothelioma and
adenocarcinoma is currently based on the use of a panel of antibodies
to adenocarcinoma-associated antigens and a few antibodies to mesothel
ial-associated antigens. Since the introduction of epitope retrieval m
ethods, the sensitivity of many antibodies has been enhanced. Thus, a
reevaluation of the mesothelioma/adenocarcinoma diagnostic panel becom
es necessary. We studied 268 paraffin-embedded formalin-fixed tumor sa
mples that included 57 epithelial mesotheliomas and 211 adenocarcinoma
s of various origins, comparing an extensive antibody panel with and w
ithout heat-induced epitope retrieval (HIER). Marked increase in the s
ensitivity of several antibodies, with no loss of specificity, was fou
nd when HIER was used. After statistical analysis, the antibodies to t
he epithelial glycoproteins carcinoembryonic antigen, BerEp4, and Bg8
emerged as the best discriminators between adenocarcinoma and epitheli
al mesothelioma within the entire panel. The mesothelium-associated an
tibodies, HBME-1, calretinin, and thrombomodulin were less sensitive a
nd less specific than the former, although they were found to be usefu
l on certain cases. Antibodies to cytokeratins and vimentin, although
of minor diagnostic value in this context, may be helpful to evaluate
the quality of antigen preservation. This study confirms the value of
immunohistochemistry to accurately distinguish mesothelioma from adeno
carcinoma when an antibody panel approach is used. The addition of hea
t-induced epitope retrieval methods increases the effectiveness of the
procedure and is recommended for most of the antibody panel members.