1989
DOI: 10.1002/1097-0142(19890515)63:10<2024::aid-cncr2820631026>3.0.co;2-h
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Flow cytometric surface light chain analysis of lymphocyte-rich effusions. A useful adjunct to cytologic diagnosis

Abstract: The cytologic diagnoses in 49 body cavity fluids from 46 patients, of whom 30 had a clinical diagnosis of lymphoma or lymphatic leukemia, and 16 patients with benign inflammatory or reactive conditions, were compared to flow cytometric surface immunoglobulin light chain analysis (kappa-lambda analysis [KLA]). The results of both tests were correlated with clinical outcome and all available information from biopsy, autopsy, and additional cell marker studies. When the diagnoses by both cytologic analysis and KL… Show more

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Cited by 11 publications
(4 citation statements)
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“…Analysis of cell-surface markers was performed by flow cytometry on fresh samples of pleural fluid, as previously described, with monoclonal antibodies directed against CD3, CD5, CD10, CD13, CD14, CD19, CD20, CD33, CD38, and CD45 (all from Becton Dickinson, San Jose, Calif.) and CDIIb (Immunotech, Marseilles, France). 28 For ultrastructural analysis, cells from fresh samples of pleural fluid were fixed first in paraformaldehyde-glutaraldehyde and then in osmium tetroxide, embedded in Epon, sectioned, and stained with uranyl acetate. Structural features were compared with those of primary-effusion-lymphoma-derived cells that have been shown to support the replication of HHV-8.…”
Section: Cytologic Immunophenotypic and Ultrastructural Studiesmentioning
confidence: 99%
“…Analysis of cell-surface markers was performed by flow cytometry on fresh samples of pleural fluid, as previously described, with monoclonal antibodies directed against CD3, CD5, CD10, CD13, CD14, CD19, CD20, CD33, CD38, and CD45 (all from Becton Dickinson, San Jose, Calif.) and CDIIb (Immunotech, Marseilles, France). 28 For ultrastructural analysis, cells from fresh samples of pleural fluid were fixed first in paraformaldehyde-glutaraldehyde and then in osmium tetroxide, embedded in Epon, sectioned, and stained with uranyl acetate. Structural features were compared with those of primary-effusion-lymphoma-derived cells that have been shown to support the replication of HHV-8.…”
Section: Cytologic Immunophenotypic and Ultrastructural Studiesmentioning
confidence: 99%
“…The differential diagnosis of secondary involvement by a lymphoma composed predominantly of small cells (e.g., lymphoblastic lym-phoma) includes a benign lymphocytic effusion like that resulting from tuberculosis. 14 In the case of the less common T-cell lymphoma, a T-cell phenotype with aberrant markers can be demonstrated by immunocytochemistry or flow cytometry, confirming a malignant diagnosis. The cells of small lymphocytic lymphoma are virtually impossible to distinguish from small, mature lymphocytes with Papanicolaou-stained preparations, even with the help of computer-assisted morphometry.…”
Section: Differential Diagnosis Of Secondary Involvement By Lymphomamentioning
confidence: 99%
“…28,31,32 The technique can be quite useful in the workup of lymphocytic effusions, espe-cially when the lymphocytic effusion is composed of small lymphoid cells and differentiation from reactive processes, such as tuberculosis, is difficult. The diagnostic utility of immunophenotyping of obviously malignant lymphoid cells is less certain, although classification as to whether a B-or T-cell lymphomatous effusion is present may be useful in selective cases.…”
Section: Flow Cytometrymentioning
confidence: 99%