S. Suster et al., EXPRESSION OF BCL-2 ONCOPROTEIN IN BENIGN AND MALIGNANT SPINDLE-CELL TUMORS OF SOFT-TISSUE, SKIN, SEROSAL SURFACES, AND GASTROINTESTINAL-TRACT, The American journal of surgical pathology, 22(7), 1998, pp. 863-872
An immunohistochemical study to determine the pattern of immunoreactiv
ity for bcl-2 oncoprotein was performed in 380 spindle cell tumors of
soft tissue, skin, serosal surfaces, and gastrointestinal tract. The c
ases studied included examples of benign, reactive spindle cell prolif
erations to benign and malignant spindle cell neoplasms, including nod
ular fasciitis (10), fibromatosis (5), dermatofibroma (10), dermatofib
rosarcoma protuberans (18), Kaposi's sarcoma (15), spindle cell lipoma
tous tumors (24), benign and malignant smooth muscle tumors (35), neur
al/peripheral nerve sheath neoplasms (53), synovial sarcomas (70) soli
tary fibrous tumors of serosal surfaces and other sites (56), gastroin
testinal stromal tumors (GIST) (47), and malignant undifferentiated fi
broblastic spindle cell proliferations of soft tissue (37 cases). The
results of bcl-2 staining was additionally correlated with CD34 immuno
reactivity. Bcl-2 was uniformly negative in all cases of nodular fasci
itis, fibromatosis, and dermatofibroma, as well as in benign and malig
nant smooth muscle proliferations. Strong positivity for bcl-2 was obs
erved in all cases of spindle cell lipoma, dendritic fibromyxolipoma,
Kaposi's sarcoma, solitary fibrous tumors, gastrointestinal stromal tu
mors, and in the spindle cell component of synovial sarcoma. With the
exception of the last, there appeared to be a close correlation betwee
n the expression of bcl-2 and CD34 in these tumors. Strong bcl-2 posit
ivity also was found, at least focally, in approximately one third of
benign and malignant peripheral nerve sheath tumors, particularly in t
he better-differentiated (Antoni type A) areas. Sarcomas of fibroblast
ic type, including low-grade myxofibrosarcoma, malignant fibrous histi
ocytoma, and fibrosarcoma, showed variable expression of bcl-2 in the
tumor cells. Our results appear to indicate that bcl-2 may have a wide
distribution among benign and malignant spindle cell neoplasms. Stron
g expression of this marker in some of these conditions, particularly
solitary fibrous tumor, gastrointestinal stromal tumors, and synovial
sarcoma, may be of aid for differential diagnosis.