A. Gloghini et al., KP1 CD68 EXPRESSION IN MALIGNANT NEOPLASMS INCLUDING LYMPHOMAS, SARCOMAS, AND CARCINOMAS/, American journal of clinical pathology, 103(4), 1995, pp. 425-431
Expression of KP1/CD68 macrophage-associated antigen in a series of 84
0 selected malignant neoplasms, including immunomorphologically charac
terized cases of non-Hodgkin's lymphoma (NHL) (434), Hodgkin's disease
(HD) (115), soft tissue sarcoma (147), carcinoma (49), and other tumo
rs (95), was examined. KP1 expression was detected in a significant nu
mber of NHLs (107 of 434; 24.7%), most of them (65 of 107; 60.7%) of t
he diffuse small cell subtype. Only 14 of the 155 large cell lymphomas
, compared to 10 of the 51 Ki-1/CD30+ anaplastic large cell (ALC) lymp
homas examined, were KP1 positive. Conversely, none of the T-lineage N
HL-other than Ki-1/CD30+ ALC lymphomas-or the HD cases tested was labe
led by KP1 antibody. Among the other neoplasms tested, KP1 was reactiv
e with a variable proportion of cases of malignant fibrous histiocytom
a (19 of 24; 79.2%), malignant schwannoma (8 of 22; 36.4%), liposarcom
a (3 of 9; 33.3%), leiomyosarcoma (8 of 37; 21.6%), cutaneous or metas
tatic melanoma (51 of 73; 69.9%), and renal cell carcinoma (3 of 5; 60
%). These results indicate that KP1 shows a relatively wide spectrum o
f immunoreactivity with malignant neoplasms of presumed non-histiocyte
origin, thus arguing against its expected specificity and high value
in diagnostic pathology. Although the significance of KP1 expression b
y some subsets of NHLs remains to be elucidated, its close association
with B-cell NHLs, mostly of the diffuse small cell type, should stimu
late further pathologic and clinical investigations.