Sex differences in prognosis of childhood T-cell leukemia
β Scribed by Penchansky, Lila ;Whiteside, Theresa L. ;Wollman, Michael R. ;Albo, Vincent C.
- Publisher
- John Wiley and Sons
- Year
- 1982
- Tongue
- English
- Weight
- 489 KB
- Volume
- 10
- Category
- Article
- ISSN
- 0098-1532
No coin nor oath required. For personal study only.
β¦ Synopsis
Abstract
Bone marrows of 41 untreated children and adolescents with acute lymphocytic leukemia were studied by combined immunologic and histochemical methods at the time of diagnosis. Eleven were classified as Tβcell lymphoblastic leukemias (27%) on the basis of cytochemical stains and Eβrosette assay. The patients in this group had low median age of 8 years, relatively low median WBC of 13.4 Γ 10^3^/cc, 6/11 were female, and only 2/5 males had a mediastinal mass. The girls had a lower median age than boys (7 vs 9 years), none had mediastinal masses or extramedullary involvement, and their survival was >27 months compared to 14 months for the boys (P < 0.01). All patients were enrolled and treated on the (then) currently active CCSG protocols for ALL. This study emphasizes the fact that not all patients with Tβcell ALL have poor prognosis, that sex could be an important factor affecting survival, and that the difference in survival could not be adequately explained by differences in the initial WBC.
π SIMILAR VOLUMES
analysis, the patients were divided into two groups: those with the leukemia type ATL and those with the lymphoma type. The prognostic factors have been evaluated separately for each of the types as well.
The concentration of T-cell receptor rearrangement excision DNA circles (TRECs) in peripheral blood mononuclear cells (PBMCs) is currently known to be a marker of recent thymic emigrants. We evaluated the hypothesis that TREC values would be lower in childhood T-cell hematopoietic malignancies than
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.
## Background. For T-malignancies in children a poor prognosis is reported. In these malignancies a combination of lymphoma and leukemia is commonly seen at presentation and most patients are treated according to protocols for acute lymphoblastic leukemia (ALL). These protocols are often designed