Application of flow cytometry in diagnosis of T-cell rich diffuse large B-cell lymphoma.
- Author:
Cheng-qing XIA
1
;
Man QI
;
Xian-fa XU
;
Li-hong LI
;
Hong-ying ZHAO
Author Information
- Publication Type:Journal Article
- MeSH: Aged; Antigens, CD19; metabolism; Antigens, CD20; metabolism; Diagnosis, Differential; Female; Flow Cytometry; methods; Humans; Immunoglobulin lambda-Chains; metabolism; Immunohistochemistry; Leukocyte Common Antigens; metabolism; Lymphoma, Large B-Cell, Diffuse; diagnosis; metabolism; Male; Middle Aged; T-Lymphocytes; metabolism; pathology
- From: Chinese Journal of Pathology 2007;36(1):29-32
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo investigate the application of flow cytometry in diagnosis of T-cell rich diffuse large B-cell lymphoma.
METHODSHistopathologic features, immunohistochemical findings and flow cytometry results of three cases of T-cell rich diffuse large B-cell lymphoma were reviewed retrospectively.
RESULTSIn CD45-side scatter (SSC) dot plot of the first patient, two different CD45-positive lymphoid cell populations were identified. The bright population consisted of both T and B cells, with a T-cell predominance. The dim population consisted mainly of B cells which showed lambda light chain restriction. In the second patient, CD45-positive cells were subdivided into two groups according to CD45-SSC dot plot. The small population consisted of both T and B cells, with a T-cell predominance. The large population consisted mainly of B cells which showed kappa light chain restriction. In the third patient, CD19-positive cells were subdivided into two groups according to the expression of CD20 in CD19-CD20 dot plot. The CD20-positive population expressed both kappa and lambda light chains, while the CD20-negative population demonstrated kappa light chain restriction.
CONCLUSIONSNeoplastic B cells can be distinguished from reactive lymphoid cells in T-cell rich diffuse large B-cell lymphoma by flow cytometry, according to a number of parameters which include intensity of antigen expression, loss of antigens, expression of non-B-cell lineage antigens, patterns of forward scatter (FSC) and/or SSC, and expression of immature B-cell antigens.