Cutaneous presentation of B-cell chronic lymphocytic leukaemia (B-CLL) is uncommon, and the influence of skin changes on B-CLL prognosis is unclear. We report a patient with B-CLL Rai II, with multiple nodular skin infiltrations on the trunk, upper arms and thighs as well as constitutional symptoms,
Telomeric associations in a patient with B-cell prolymphocytic leukaemia
β Scribed by Dr. Rodney T. Howell; Clare Kitchen; Graham R. Standen
- Publisher
- John Wiley and Sons
- Year
- 1993
- Tongue
- English
- Weight
- 270 KB
- Volume
- 7
- Category
- Article
- ISSN
- 1045-2257
No coin nor oath required. For personal study only.
β¦ Synopsis
Telomeric associations were determined in bone marrow preparations from a patient with 6-cell prolymphocytic leukaemia and a clonal isochromosome of the long arm of chromosome 17. Thirteen associations involved 16 chromosome arms, with preferential involvement of the short arm of chromosome 19 and the long arm of 17. Genes Chrom Cancer 7:116-118 (1993).
π SIMILAR VOLUMES
## Abstract Leukaemic Bβcell populations were prepared from six patients with highβcount prolymphocytic leukaemia (PLL) as well as from one patient with WaldenstrΓΆm's macroglobulinaemia (WM) in frankly leukaemic phase, and their response to __in vitro__ EpsteinβBarr (EB) virus infection was monitor
Ataxia telangiectasia (A-T) is an autosomal recessive disorder in which patients show an unusual predisposition to malignant disease, including T-cell chronic lymphocytic leukaemia. We report here the steady growth over 5 years of a complex, cytogenetically abnormal clone of T lymphocytes in an A-T