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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
1996-10-16
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pubmed:abstractText |
Sezary syndrome is defined as the leukemic variation of cutaneous T-cell lymphomas. Here we describe the cytogenetic pattern of peripheral T-cells of a 50-year-old male patient suffering from this disease. We used Giemsa-banding (G-banding) technique and a fluorescence in situ hybridization (FISH) assay to determine cytogenetic changes affecting 15 different chromosomes. The cells displayed an abnormal hypodiploid karyotype with a prominent insertion located at the short arm of chromosome 1. Unbalanced translocations were observed involving chromosomes 4 and 14. Besides other abnormalities we detected a 6q- deletion. These multiple genetic changes may reflect the high aggressivity of the neoplastically transformed T-cell population and the poor response to chemotherapeutic treatment.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:status |
MEDLINE
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pubmed:month |
Aug
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pubmed:issn |
0165-4608
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
90
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
33-6
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pubmed:dateRevised |
2007-11-15
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pubmed:meshHeading |
pubmed-meshheading:8780744-Aneuploidy,
pubmed-meshheading:8780744-CD4-Positive T-Lymphocytes,
pubmed-meshheading:8780744-CD8-Positive T-Lymphocytes,
pubmed-meshheading:8780744-Chromosome Aberrations,
pubmed-meshheading:8780744-Chromosome Banding,
pubmed-meshheading:8780744-Fatal Outcome,
pubmed-meshheading:8780744-Humans,
pubmed-meshheading:8780744-Immunophenotyping,
pubmed-meshheading:8780744-In Situ Hybridization, Fluorescence,
pubmed-meshheading:8780744-Male,
pubmed-meshheading:8780744-Middle Aged,
pubmed-meshheading:8780744-Neoplastic Stem Cells,
pubmed-meshheading:8780744-Sezary Syndrome
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pubmed:year |
1996
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pubmed:articleTitle |
Complex cytogenetic and immunophenotypic aberrations in a patient with Sezary syndrome.
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pubmed:affiliation |
Universitätsklinikum Carl Gustav Carus der Technischen Universität Dresden, Germany.
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pubmed:publicationType |
Journal Article,
Case Reports
|