Ap. Deitos et al., IMMUNOHISTOCHEMICAL DEMONSTRATION OF GLYCOPROTEIN P30 32(MIC2) (CD99)IN SYNOVIAL SARCOMA - A POTENTIAL CAUSE OF DIAGNOSTIC CONFUSION/, Applied immunohistochemistry, 3(3), 1995, pp. 168-173
Immunohistochemical demonstration of the MIC2 gene product (CD99) repr
esents a valuable diagnostic tool that makes identification of periphe
ral primitive neuroectodermal tumors easier. Different commercially av
ailable antibodies have been raised that show a high sensitivity along
with a specificity that is widely regarded as acceptable although not
absolute. MIC2 expression has been reported in lymphoblastic lymphoma
, occasionally in several other types of sarcoma, and in some neuroend
ocrine tumors and ependymomas. The recent personal observation of immu
nopositivity for MIC2 gene product in some synovial sarcomas that had
been difficult to diagnose prompted us to undertake a systematic study
of a larger series of 50 synovial sarcomas, of which 62% showed posit
ive immunoreactivity for either 013 (Signet) or 12E7 (Dako MIC2). This
is the highest incidence of CD99 positivity reported to date in any t
ype of sarcoma other than the Ewing's/primitive neuroectodermal tumor
group. Immunopositivity for CD99 was common in all morphologic subtype
s of synovial sarcoma. As poorly differentiated synovial sarcoma may o
verlap morphologically with primitive neuroectodermal tumor, careful h
istologic examination along with evaluation of a wider panel of differ
entiation markers is mandatory to avoid this potential diagnostic pitf
all, which has both therapeutic and prognostic implications.