Chromosomes and causation of human cancer and leukemia. XXXIII. 5q– in a case of acute lymphoblastic leukemia (ALL)
✍ Scribed by S. Abe; S. Kohno; I. Kubonishi; J. Minowada; A. A. Sandberg
- Publisher
- John Wiley and Sons
- Year
- 1979
- Tongue
- English
- Weight
- 499 KB
- Volume
- 6
- Category
- Article
- ISSN
- 0361-8609
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
The case of a 4‐year‐old boy with ALL, possibly developing subsequent to a lymphoma involving the throacic cavity, which was shown to be of the T‐cell type, is presented. The leukemic cells had a 5q– anomaly, which had previously been described only in cases of refractory anemia and/or AML. The 5q– abnormality was invariably accompanied by a 9p– chromosome in the leukemic cells. The interstitial deletion leading to the 5q– chromosome was shown with banding techniques to be similar to that described previously in myeloproliferative disorders. Some aspects of the 5q– anomaly in ALL and its relation to previous experience with this karyotypic change are discussed.
📜 SIMILAR VOLUMES
of a de novo Ph in T-cell acute leukemia. So this case could be the first de novo T-cell childhood ALL showing the expression of p210 protein associated with a very aggressive clinical evolution.
Lineage switch from AML to ALL is an extremely rare phenomenon, and we report the case of an adult diagnosed with AML at 46 years of age who relapsed with ALL. At initial diagnosis, blast cell morphology and immunophenotyping were consistent with the diagnosis of M4-AML. Complete remission was achie