Ja. Mcbride et al., T-CELL-RICH B-LARGE-CELL LYMPHOMA SIMULATING LYMPHOCYTE-RICH HODGKINS-DISEASE, The American journal of surgical pathology, 20(2), 1996, pp. 193-201
Immunophenotypic analysis of 50 cases fulfilling the histologic criter
ia for mixed cellularity Hodgkin's disease disclosed nine cases with a
B-cell, non-Hodgkin's phenotype (CD20+, CD15-, CD30-, EMA-). The case
s were characterized by a diffuse small lymphocytic milieu, interspers
ed atypical large cells including classic Reed-Sternberg cells, and in
frequent plasma cells, eosinophils, and L&H cells. The male:female rat
io was 7:2 (aged 22-65 years, median 39 years). Three patients were An
n Arbor stage II, two stage III, and four stage IV. The patients prese
nted with generalized lymphadenopathy (four), mesenteric lymph node in
volvement (two), splenomegaly (four), and bone marrow involvement (thr
ee). Four patients were treated with standard Hodgkin's disease protoc
ols. Two attained a complete response and two a partial response; all
relapsed and died. Four of five patients treated for large-cell lympho
ma achieved a complete response and are currently alive without eviden
ce of disease. The one patient with an initial partial response relaps
ed and died. We conclude that immunophenotypic analysis is essential i
n cases of histologic mixed cellularity Hodgkin's disease, especially
in those with lymphocyte-rich morphology. Cases with a B-cell phenotyp
e should be diagnosed and treated as T-cell-rich B large-cell lymphoma
.