Jx. Oconnell et al., GIANT-CELL TUMOR OF TENDON SHEATH AND PIGMENTED VILLONODULAR SYNOVITIS - IMMUNOPHENOTYPE SUGGESTS A SYNOVIAL CELL ORIGIN, Human pathology, 26(7), 1995, pp. 771-775
Giant cell tumor of tendon sheath (GCTS) and pigmented villonodular sy
novitis (PVNS) are common synovial ''tumors.'' Their immunohistochemic
al profile, however, has not been well characterized, and uncertainty
exists regarding their histogenesis and relationship to fibroma of ten
don sheath. In an effort to clarify these uncertainties and to better
define the immunohistochemical profile of GCTS/PVNS, we examined forma
lin fixed tissue from 35 specimens of GCTS, 12 specimens of PVNS, and
three cases of reactive synovitis using avidin biotin complex (ABC) an
d streptavidin immunohistochemical methods. Antibodies to vimentin, CD
68, HAM56, cytokeratins, EMA, S100, HMB45, leukocyte common antigen, C
D34, desmin, and smooth muscle actin were used in the study. The proli
ferating mononuclear cells and surface synovial cells in GCTS/PVNS and
reactive synovitis: stained positively for CD68, HAM56, and vimentin
only. Multinucleated cells stained for CD68, vimentin, and leukocyte c
ommon antigen. Ah other stains were negtive. Our results suggest that
GCTS/PVNS are tumors of synovial cell origin, and do not support an as
sociation between GCTS and fibroma of tendon sheath. Copyright (C) 199
5 by W.B. Saunders Company