Cytogenetic study of a patient with the Sézary syndrome

F. Solé, N. Tarrida, M. D. Coll, M. R. Caballin, A. De Miguel, S. Woessner, J. Egozcue

Research output: Contribution to journalArticleResearchpeer-review

6 Citations (Scopus)

Abstract

A cytogenetic study was performed in a patient with Sézary syndrome, which is a T-helper lymphoproliferative disorder. Metaphases were obtained from a phytohemaglutinin-stimulated lymphocyte culture. Normal, hypodiploid (42 to 45 chromosomes) and hypotetraploid (84 to 88 chromosomes) cells were observed. Both abnormal cell lines showed the same abnormalities involving chromosomes 1, 2, 4, 6, 10, 11, 12, 14, 16, and 20. © 1990.
Original languageEnglish
Pages (from-to)193-196
JournalCancer Genetics and Cytogenetics
Volume44
DOIs
Publication statusPublished - 1 Jan 1990

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