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PMID: 6882921 Published · ppublish English Case Reports Journal Article Research Support, U.S. Gov't, P.H.S.

Possible specific chromosome change in prolymphocytic leukemia.

Blood ·Vol. 62 ·No. 4 ·1983-10-00 ·Pages 729-36

Sadamori N, Han T, Minowada J, Bloom ML, Henderson ES, Sandberg AA

Abstract

The chromosomes of unstimulated and stimulated blood lymphocytes from 5 cases with B-cell prolymphocytic leukemia (PLL) were examined following the use of polyclonal B-cell activators (PBA). Banding techniques revealed a common and specific chromosome abnormality to be present in each of the cases, which was due to a translocation between chromosomes 6 and 12 (t(6;12)(q15;p13]. The fact that this specific chromosome change has not been reported in other lymphoproliferative disorders may indicate that PLL is a distinct clinical entity and different from other lymphoproliferative disorders, whether it occurs de novo or complicates chronic lymphocytic leukemia (CLL).

MeSH Terms
Aged Chromosome Aberrations Chromosomes, Human, 1-3 Chromosomes, Human, 16-18 Chromosomes, Human, 19-20 Chromosomes, Human, 21-22 and Y Chromosomes, Human, 6-12 and X Female Humans Karyotyping Leukemia, Lymphoid/genetics Male Sex Chromosomes
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Sadamori N
Han T
Minowada J
Bloom M L
Henderson E S
Sandberg A A
Article Info
Journal
Blood
Abbr.
Blood
ISSN
0006-4971
Published
1983-10-00
Pages
729-36
Language
English
Region
United States
NLM ID
7603509
Subset
IM
Grants
NCI NIH HHS · CA-14555 · United States
NCI NIH HHS · CA-5834 · United States
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