Rk. Brynes et al., NUMERICAL CYTOGENETIC ABNORMALITIES OF CHROMOSOME-3, CHROMOSOME-7, AND CHROMOSOME-12 IN MARGINAL ZONE B-CELL LYMPHOMAS, Modern pathology, 9(10), 1996, pp. 995-1000
Monocytoid B-cell lymphoma, low-grade B-cell lymphoma of mucosa-associ
ated lymphoid tissue, and primary splenic marginal zone cell lymphoma
(SMZCL) were originally described as distinct clinicopathologic entiti
es. On the basis of morphologic and immunologic similarities, monocyto
id B-cell lymphoma and lymphoma of mucosa-associated lymphoid tissue r
ecently have been grouped together as nodal and extranodal types of ma
rginal zone B-cell lymphomas (MZBCLs) in the Revised European-American
Classification of Lymphoid Neoplasms. Primary SMZCL, although related
, is considered a separate provisional entity. Trisomies 3, 7, and 12
are common in non-Hodgkin's lymphomas, Several recent studies reported
that MZBCLs arising in sites of mucosa-associated lymphoid tissue hav
e a high frequency of trisomy 3. To assess whether similar numerical c
ytogenetic abnormalities are present in MZBCLs with prominent monocyto
id B-cell cytologic features, we performed a retrospective study, usin
g formalin-fixed, paraffin-embedded tissue blocks from 36 cases. By us
e of fluorescence in Situ hybridization to detect chromosome trisomies
, we identified trisomy 3 in 11 (85%) of 13 extranodal MZBCLs with mon
ocytoid B cells (MZBCL-Es), in 6 (50%) of 12 nodal MZBCLs of monocytoi
d B-cell type (MZBCL-Ns), but in only 2 (18%) of 11 SMZCLs. Trisomies
7 and 12 were found at lower frequencies. These data suggest that tris
omy 3 is a common numerical chromosomal abnormality of MZBCL-Es and MZ
BCL-Ns with monocytoid B-cell features. Despite similar morphologic an
d immunophenotypic characteristics, the low incidence of trisomy 3 in
the SMZCL cases implies that this process may be genetically distinct.