Persistent polyclonal B-cell lymphocytosis (PPBL) is a rare entity of unknown etiology characterized by a polyclonal expansion of B-lymphocytes with typical bilobulated forms, elevated serum IgM, and an additional isochromosome for the long arm of chromosome 3 as the sole change. In the present stud
โฆ LIBER โฆ
Polyclonal B-cell lymphocytosis and hypergammaglobulinemia in patients with gaucher disease
โ Scribed by Dr. G. E. Marti; E. T. Ryan; N. M. Papadopoulos; M. Filling-Katz; N. Barton; T. A. Fleischer; M. Rick; H. R. Gralnick
- Publisher
- John Wiley and Sons
- Year
- 1988
- Tongue
- English
- Weight
- 512 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0361-8609
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## Abstract ## Background: Monoclonal Bโcells can be detected in the peripheral blood of some adults without Bโcell malignancies, a condition recently termed monoclonal Bโcell lymphocytosis (MBL). The risk of individuals with MBL progressing to a Bโcell malignancy is unknown. Polyclonal Bโcell lym
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