NUMERICAL CYTOGENETIC ABNORMALITIES OF CHROMOSOME-3, CHROMOSOME-7, AND CHROMOSOME-12 IN MARGINAL ZONE B-CELL LYMPHOMAS

Citation
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
Citations number
31
Categorie Soggetti
Pathology
Journal title
ISSN journal
08933952
Volume
9
Issue
10
Year of publication
1996
Pages
995 - 1000
Database
ISI
SICI code
0893-3952(1996)9:10<995:NCAOCC>2.0.ZU;2-4
Abstract
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.