Abstract
This report deals with a case of Sézary syndrome, a rare peripheral T-cell lymphoproliferative disorder, in which cytogenetic analysis performed during the disease transformation revealed the presence of a t(9;22) (q34;q11.2) translocation. Molecular analyses identified a new transcript, an e8a4 BCR-ABL fusion mRNA which could be responsible for the disease transformation.
Publication types
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Case Reports
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Letter
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Research Support, Non-U.S. Gov't
MeSH terms
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Aged
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Chromosomes, Human, Pair 22 / genetics
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Chromosomes, Human, Pair 9 / genetics
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Fatal Outcome
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Female
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Fusion Proteins, bcr-abl / genetics*
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Humans
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In Situ Hybridization, Fluorescence
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Karyotyping
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Sezary Syndrome / diagnosis
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Sezary Syndrome / drug therapy
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Sezary Syndrome / genetics*
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Translocation, Genetic