IMMUNOHISTOCHEMICAL PROFILE OF MONOCLONAL-ANTIBODY O-13 - ANTIBODY THAT RECOGNIZES GLYCOPROTEIN P30 32(MIC2) AND IS USEFUL IN DIAGNOSING EWINGS-SARCOMA AND PERIPHERAL NEUROEPITHELIOMA/
N. Weidner et J. Tjoe, IMMUNOHISTOCHEMICAL PROFILE OF MONOCLONAL-ANTIBODY O-13 - ANTIBODY THAT RECOGNIZES GLYCOPROTEIN P30 32(MIC2) AND IS USEFUL IN DIAGNOSING EWINGS-SARCOMA AND PERIPHERAL NEUROEPITHELIOMA/, The American journal of surgical pathology, 18(5), 1994, pp. 486-494
Ewing's sarcoma (ES) and peripheral neuroepithelioma (PN) are closely
related tumors, and it can be difficult to distinguish them from other
small-round-cell tumors (SRCTs). The glycoprotein p30/32(MIC2) is hig
hly, but not exclusively, expressed in both ES and PN. Although the mo
noclonal antibody (Mab) HBA71, which reacts with p30/32(MIC2), has bee
n reported to be relatively specific and highly sensitive for both neo
plasms, it is not readily available. Yet, Mab O13 is commercially avai
lable, and it purportedly displays the same immunostaining characteris
tics as HBA71. Because O13 has not been studied extensively, we immuno
stained 21 ES/PNs and 147 other tumors or lesions that might show SRCT
-like features with O13. The results were similar to those reported fo
r HBA71. We found O13 to be 100% sensitive for ES/PN; and, no immunost
aining was noted on the SRCTs often included in the differential diagn
osis of ES/PN (i.e., conventional neuroblastoma, rhabdomyosarcoma, and
nonlymphoblastic lymphomas). But, O13 immunoreacted with lymphoblasti
c lymphomas and some other tumors and normal tissues. Nonetheless, thi
s nonspecific reactivity should not cause diagnostic problems, if an a
ntibody panel containing anti-desmin and anti-leukocyte common antigen
is used in conjunction with O13. We conclude that, within the proper
diagnostic context, strong immunoreactivity of a SRCT tumor for O13 sh
ould be considered good evidence that the tumor is ES/PN.