St. Traweek et al., EXTRAMEDULLARY MYELOID CELL TUMORS - AN IMMUNOHISTOCHEMICAL AND MORPHOLOGIC STUDY OF 28 CASES, The American journal of surgical pathology, 17(10), 1993, pp. 1011-1019
In an attempt to correlate the morphologic and immunophenotypic findin
gs in extramedullary myeloid cell tumors (EMT), we studied 28 cases wi
th a large panel of antibodies using paraffin section immunohistochemi
stry. A previous or concurrent diagnosis of acute myelogenous leukemia
or chronic myelogenous leukemia was made in 25 cases. Six EMT were mo
rphologically classified as well differentiated (WD-EMT), 17 as poorly
differentiated (PD-EMT), and five as blastic EMT. The WD-EMT were eas
ily recognized morphologically and displayed a relatively mature myelo
id phenotype, with elastase, CD15, and CD68 positivity in all cases. O
n the other hand, the five blastic-EMT displayed no morphologic eviden
ce of myeloid derivation, were completely negative for CD15, and were
weakly positive for elastase in only one case. The PD-EMT, with a morp
hologic appearance that resembles large cell non-Hodgkin's lymphoma, v
ariably expressed CD15 and elastase. CD68 and lysozyme were present in
the majority of PD-EMT, with some variability, but were negative in m
ost blastic-EMT. CD45 (LCA) was detected in 75% of all EMT and CD34 wa
s positive in 36%; neither antigen was significantly associated with a
specific morphology. CD30 reactivity was not evident in any case, but
slight positive staining was seen with CD20 (L26) in one WD-EMT. CD43
(Leu 22) was the only antibody that was positive in 100% of cases; st
aining was always intense and widespread. Antimyeloperoxidase (MPO) wa
s positive in all cases but two, both with a blastic morphology. We co
nclude that (a) an immunohistochemical panel including CD20, CD43, CD6
8, and MPO can successfully identify the vast majority (96%) of EMT in
paraffin sections, and (b) there is an association between morphology
and phenotype in these lesions.