Diagnostic features and survival in typical and prolymphocytoid variants of chronic lymphocytic leukemia
β Scribed by Dr. Colin Stephen Scott; Allistair N. Stark; Christine Head; Bryon E. Roberts
- Publisher
- John Wiley and Sons
- Year
- 1989
- Tongue
- English
- Weight
- 349 KB
- Volume
- 7
- Category
- Article
- ISSN
- 0278-0232
No coin nor oath required. For personal study only.
β¦ Synopsis
Diagnostic features were evaluated with regards to survival in 203 cases of typical and prolymphocytoid chronic lymphocytic leukemia. Excluding 27 (1 3 per cent) patients with second malignancies, survival analyses indicated that the prognostic factors with greatest significance were age at presentation ( < 65 years and 65 years or more: p=0.0004), proportions of prolymphocytoid cells (< 10 per cent and I0 per cent or more:p < 0.0001 age corrected) and surface immunoglobulin (SIg) density (weak and more than weak: p=O.OOl age corrected). In contrast, sex, absolute numbers of prolymphocytoid cells, SIg light chain type and FMC7 expression were not prognostically significant. These observations suggest that the recognition and delineation of prolymphocytoid CLL variants by morphological and immunophenotypic criteria, although important in diagnostic terms, may have less relevance with respect to prognosis and patient management.
π SIMILAR VOLUMES
A patient with long-standing chronic lymphocytic leukemia with both humoral and cellular immunodeficiency had lymph node receptor evidence of a B lymphocyte disorder. He was also found to secrete the Epstein--Barr virus and, late in his illness, developed a markedly positive antinuclear antibody. In
## Abstract ## BACKGROUND: Little is known about the patterns of care relating to the diagnosis of chronic lymphocytic leukemia (CLL), including the use of modern diagnostic techniques such as flow cytometry. ## METHODS: The authors used the SEERβMedicare database to identify subjects diagnosed