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Deletion 6q as a recurrent chromosomal aberration in T-cell large granular lymphocyte leukemia.

Abstract
T-cell large granular lymphocyte (T-LGL) leukemia is an uncommon disease, with limited information on karyotypic aberrations. No consistent chromosomal changes have thus far been described. We report two cases of T-LGL leukemia who presented with severe anemia. The LGL were CD3+, CD4-, CD8+, CD56-, and CD161-, with variable expression of CD94, CD158a, and CD158b, and had clonal T-cell receptor gene rearrangement. A deletion of the long arm of chromosome 6 was the sole aberration in both cases. This is the first report of a recurrent chromosomal aberration in T-LGL leukemia.
AuthorsC Man, W Y Au, A Pang, Y L Kwong
JournalCancer genetics and cytogenetics (Cancer Genet Cytogenet) Vol. 139 Issue 1 Pg. 71-4 (Nov 2002) ISSN: 0165-4608 [Print] United States
PMID12547164 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Antigens, CD
Topics
  • Antigens, CD (genetics)
  • Burkitt Lymphoma (genetics)
  • Chromosome Aberrations
  • Chromosome Mapping
  • Chromosomes, Human, Pair 6
  • Humans
  • Karyotyping

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