Abstract |
We report a case of Sezary syndrome with two abnormal CD4+ T-cell populations detected in the peripheral blood by flow cytometry immunophenotyping and DNA cell content, suggesting a biclonal T-cell lymphoproliferative disorder. Despite these findings, molecular analysis of the T-cell receptor genes was consistent with a monoclonal T-cell proliferation, supporting the existence of intraclonal diversity rather than a true biclonal disease. The patient achieved a transient response with 2-deoxycoformycin, with a selective decrease of the larger/hyperploid T-cell population; later on, an increased representation of this T-cell population was observed concomitantly with clinical relapse.
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Authors | Elisa Granjo, Margarida Lima, José Manuel Lopes, Nória Cunha, Maria Dos Anjos Teixeira, Filipe Santos, Jorge Candeias, Carlos Resende, Ana Helena Santos, Ana Balanzategui, Alberto Orfão, Estella Matutes |
Journal | British journal of haematology
(Br J Haematol)
Vol. 119
Issue 3
Pg. 629-33
(Dec 2002)
ISSN: 0007-1048 [Print] England |
PMID | 12437636
(Publication Type: Case Reports, Journal Article)
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Chemical References |
- Antibiotics, Antineoplastic
- Pentostatin
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Topics |
- Aged
- Antibiotics, Antineoplastic
(therapeutic use)
- CD4-Positive T-Lymphocytes
(immunology)
- Cell Division
- Flow Cytometry
- Humans
- Immunophenotyping
(methods)
- Male
- Pentostatin
(therapeutic use)
- Phenotype
- Sezary Syndrome
(drug therapy, immunology)
- Skin Neoplasms
(drug therapy, immunology)
- T-Lymphocyte Subsets
(immunology)
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