dic(9; 20): A new recurrent chromosome abnormality in adult acute lymphoblastic leukemia
✍ Scribed by Harald Rieder; Susanne Schnittger; Heinrich Bodenstein; Martin Schwonzen; Bernhard Wörmann; Dinko Berkovic; Wolf-Dieter Ludwig; Dieter Hoelzer; Prof. Dr. Christa Fonatsch
- Book ID
- 102846833
- Publisher
- John Wiley and Sons
- Year
- 1995
- Tongue
- English
- Weight
- 677 KB
- Volume
- 13
- Category
- Article
- ISSN
- 1045-2257
No coin nor oath required. For personal study only.
✦ Synopsis
Loss of chromosome 20 and rearrangement of the short arm of chromosome 9 were identified by banding analysis of three adult patients with acute lymphoblastic leukemia (ALL). The G-banding pattern suggested an identical deletion of 9p, but, also, an unbalanced translocation with chromosome 20 was taken into consideration. Dual-color chromosome painting with probes for chromosomes 9 and 20 revealed the presence of material from chromosome 20 at the short arm of the abnormal chromosome 9 in all three cases. Centromeric alpha-satellite DNA of both chromosome 9 and chromosome 20 was demonstrated by fluorescence in situ hybridization and indicated the presence of a dicentric chromosome. The hybridization of a YAC clone of the short arm of chromosome 20 proved that the dicentric chromosome contained the short arm of chromosome 20, which had been suspected from the G-banding pattern. Thus, the rearrangement was interpreted as dic(9;20)(pl I;ql I .? I). Because this was the sole chromosome abnormality in two patients, dic(9;20) may be a primary chromosome aberration in ALL. In one case, a 9q+ chromosome derived from a Philadelphia (Ph) translocation was involved in the formation of the dicentric chromosome. lmmunophenotyping revealed C D lo+ B-cell precursor ALL in all three cases. Whereas the two patients in whom dic(9;20) was the sole cytogenetically detectable change are in continuous complete remission for I0 and 45 months, respectively, the Ph+ patient relapsed with leukemia and died 8 months after diagnosis. Genes Chromosom Cancer 1354-61 (1995).
📜 SIMILAR VOLUMES
A new chromosome anomaly in acute lymphoblastic leukemia (ALL) is reported. Three, possibly four, patients showed an identical karyotype anomaly, characterized by a (4;11)(q13;q22) reciprocal translocation. This anomaly has not so far been found in lymphoproliferative disorders other than ALL. Two o
We report a lS-month+ld boy with acute leukemic cells demonstrated a translocation myelornonocytic leukemia [French-Ameri-46,XY, t(9;11)(p24;q12) that has not been d e can-British classification M4 (FAB-M4)] whose scribed previously.