IMMUNOREACTIVITY PATTERNS OF CD31 AND CD68 IN 28 CASES OF KAPOSIS-SARCOMA - EVIDENCE SUPPORTING ENDOTHELIAL DIFFERENTIATION IN THE SPINDLE-CELL COMPONENT
Hd. Hoerl et Jr. Goldblum, IMMUNOREACTIVITY PATTERNS OF CD31 AND CD68 IN 28 CASES OF KAPOSIS-SARCOMA - EVIDENCE SUPPORTING ENDOTHELIAL DIFFERENTIATION IN THE SPINDLE-CELL COMPONENT, Applied immunohistochemistry, 5(3), 1997, pp. 173-178
The histogenesis of Kaposi's sarcoma (KS), especially the spindle cell
component, has been a subject of debate for many years. Although most
researchers have favored vascular endothelium as the cellular origin
of KS, lymphatic endothelium, interstitial stem cells, and macrophages
have also been proposed. Twenty-eight cases of KS were studied with a
ntibodies to CD31, an antigen purported to be both sensitive and speci
fic for endothelial differentiation, and the monocyte/macrophage marke
r CD68. Cases chosen for study were of tissues from a variety of anato
mic sites, including skin (both patch/plaque and nodular forms), gastr
ointestinal (GI) tract, lung, and lymph nodes. Nineteen of 28 (68%) pa
tients were infected with the human immunodeficiency virus (HIV); one
patient had undergone previous renal transplantation. CD31 stained the
endothelial cell lining of small vessels in all cases of KS. In addit
ion, CD31 also stained the spindle cell component in 25 of 28 (89%) ca
ses, typically in a strong and diffuse pattern. Staining was found in
14 of 17 cases of cutaneous KS (eight of 10 cases of patch/plaque stag
e; six of seven cases of nodular stage), five of five cases of GI KS,
three of three cases of nodal KS, and three of three cases of pulmonar
y KS. Eighteen of 19 (95%) of the HIV-positive patients had CD31-posit
ive tumors in the spindle cell component. Focal, weak CD68 staining wa
s seen in only eight of 28 (29%) cases of KS, including three cases of
patch/plaque stage, four cases of nodular cutaneous KS, and one case
of nodal KS. Four of the eight patients with CD68-positive tumors were
HIV-positive. In conclusion, CD31 is a sensitive marker of KS from a
variety of anatomic sites, is independent of tumor stage and HIV statu
s, and provides supporting evidence of endothelial differentiation in
the spindle cell component of KS. CD68 demonstrates only weak immunore
activity in occasional spindle cells in fewer than one third of cases
of KS and is not diagnostically helpful.