[Use of the multiparametric panel CD3/CD4/CD8/CD7/CD26/CD158k in the detection and use of flow cytometry of Sezary cells]
Autor: | Florence Granel-Brocard, Julien Broséus, Jonas Callet, Arnaud Campidelli, S. Salignac, Jean-Philippe Vial, Jean-François Lesesve, Delphine Gérard, Anne-Claire Bursztejn, Véronique Latger-Cannard |
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Jazyk: | francouzština |
Rok vydání: | 2021 |
Předmět: |
Pathology
medicine.medical_specialty Skin Neoplasms medicine.drug_class CD3 Dipeptidyl Peptidase 4 CD8-Positive T-Lymphocytes Monoclonal antibody Flow cytometry Antigens CD medicine Biomarkers Tumor Humans Sezary Cell Retrospective Studies medicine.diagnostic_test biology business.industry Genetic heterogeneity General Medicine medicine.disease Flow Cytometry KIR3DL2 biology.protein business Generalized lymphadenopathy CD8 |
Zdroj: | Annales de biologie clinique. 79(3) |
ISSN: | 1950-6112 |
Popis: | The Sezary syndrome has been defined by a triad combining erythrodermia, generalized lymphadenopathy, and the presence of circulating Sezary cells > 1 × 109/L characterized by a CD4+/CD8- phenotype with loss of one or more T antigens (mainly CD7 and/or CD26). We retrospectively reviewed the immunophenotypic profiles of 10 SS patients followed in our institution (University Hospital at Nancy, France). The application of the WHO criteria resulted in a diagnostic confirmation for 9 out of 10 cases. Since 2008, new diagnostic and staging criteria have been proposed, including the CD158k/KIR3DL2 receptor detection. The application of these new criteria to our cohort led us to notice a phenotypic heterogeneity of our cases but allowed to achieve a relevant diagnosis of Sezary syndrome in all cases, especially for patients with lymphopenia. The use of such a panel of monoclonal antibodies also optimized the follow-up of the patients. |
Databáze: | OpenAIRE |
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