Utilizza questo identificativo per citare o creare un link a questo documento: http://hdl.handle.net/10556/1385
Titolo: Monoclonal B-cell lymphocytosis
Autore: D'Arena, Giovanni
Musto, Pellegrino
Parole chiave: Monoclonal B-cell lymphocytosis
Chronic lymphocytic leukemia
Diagnostic criteria
Management
Data: 2014
Citazione: D’Arena G, Musto P. Monoclonal B-cell lymphocytosis. Translational Medicine @ UniSa 2014;8(9):75-79
Abstract: Monoclonal B-cell lymphocytosis (MBL) is an asymptomatic hematologic condition defined by the presence of a small (<5 x 109/L) clonal B-cell population in the peripheral blood in the absence of lymph-node enlargement, cytopenias or autoimmune diseases. It is found in approximately 3-12% of normal persons depending on the accuracy of analytical techniques applied. According to the immunophenotypic profile of clonal B-cells, the majority of MBL cases (75%) are classified as chronic lymphocytic leukemia (CLL)-like. This form may progress into CLL at a rate of 1–2% per year. It is thought that CLL is always preceded by MBL. The remaining MBL cases are defined as atypical CLL-like (CD5+/CD20bright) and CD5- MBL. The MBL clone size is quite heterogenous. Accordingly, two forms of MBL are identified: i) high-count, or ‘clinical’ MBL, in which an evidence of lymphocytosis (<5 x 109/L clonal B-cells) is seen, and ii) a low-count MBL, in which a normal leukocyte count is found and that is identified only in population-screening studies. Both forms of MBL may carry the cytogenetic abnormalities that are the hallmark of CLL, including 13q-, 17p- and trisomy 12. Consistent with the indolent phenotype of this condition, genetic lesions, such as TP53, ATM, NOTCH1 and SF3B1 mutations, usually associated with high-risk CLL, are rarely seen. Overall, no prognostic indicator of evolution of MBL to overt CLL has been found at present time. However, taking into account this possibility, a clinical and lab monitoring (at least annually), is recommended.
URI: http://hdl.handle.net/10556/1385
http://dx.doi.org/10.14273/unisa-234
ISSN: 2239-9747
È visualizzato nelle collezioni:Translational Medicine @ UniSa. Vol.8 (jan.-mar. 2014)

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