Jl. Dargent et al., A CASE OF PLEOMORPHIC T-CELL LYMPHOMA WITH A HIGH CONTENT OF REACTIVEHISTIOCYTES PRESENTED WITH HYPEREOSINOPHILIA, Pathology research and practice, 191(5), 1995, pp. 463-468
A case of peripheral T-cell lymphoma classified, according to the upda
ted Kiel classification, as a large pleomorphic T-cell lymphoma with a
high content of reactive histiocytes and blood hypereosinophilia is r
eported. Light microscopic examination revealed a diffuse effacement o
f the lymph node structure by large pleomorphic lymphoma cells mixed w
ith eosinophils and many histiocytes, some of them presenting discrete
features of hemophagocytosis. The neoplastic cells were CD3, CD5, CD8
and HLA-DR positive but failed to show CD30 antigen. DNA molecular an
alysis displayed simultaneous rearrangements of the genes coding for t
he delta chain of the T-cell receptor and for the Ig heavy chain. Incr
eased serum levels of angiotensin converting enzyme and ferritin were
found and probably induced by the reactive histiocytes. Immunoassays (
ELISA) with antibodies directed against some cytokines and against the
Tac peptide (sIL-2R) were performed. They demonstrated high serum lev
els of sIL-2R and a slight increase in GM-CSF, but neither IL-5 nor IL
-3. The association of blood hypereosinophilia and histiocytic hyperpl
asia with a peripheral T-cell lymphoma is discussed.