Disease Waldenstrom's macroglobulinemia (corresponding to lymphoplasmacytoid lymphoma / Immunocytoma in the REAL and WHO classification) Phenotype / cell stem origin Stem cell origin: Post-germinal centre IgM-bearing memory B-cell. Phenotype: CD19+; CD20+; CD22+; FMC7+; CD38+; cytoplasmic IgM bright+; CD5-; CD23-; CD10-. Epidemiology It accounts for 1-2% of all nodal lymphomas. The annual incidence falls in the 0,2-0,6% range per 100 000. Clinics Indolent lymphoma characterized by the secretion of a monoclonal IgM protein and by the expansion of the neoplastic clone in the bone marrow, in the lymphoid tissue and in extra-nodal sites. The symptoms derive from tissue infiltration, bone marrow failure and from the presence of the IgM paraprotein (hyperviscosity syndrome, polyneuropathies, AL amyloidosis) Pathology Diffuse proliferation of small lymphocytes, plasmacytoid lymphocytes and plasma cells, infiltrating the bone marrow and the interfollicular areas of the lymph nodes. By definition, this lymphoma subtype lacks the diagnostic features chronic lymphocytic leukemia (CLL), mantle cell lymphoma and follicle centre cell lymphoma. Transformation into high grade lymphoma may occur in a minority (5%) of cases.. Treatment Alkylating agents (chlorambucil), multiagent chemotherapy (vincristine cyclophosphamide, steroid, with or without anthtacyclines); fludarabine, with or without mitoxantrone. Prognosis Median survival exceeds 5 years and there is no plateau in the survival curve, just as in other low-grade lymphomas. Cytogenetics Cytogenetics Morphological There is no chromosome anomaly that is specific for WM. The overall cytogenetic picture is similar to that of marginal zone B-cell lymphoma. Recurrent structural changes include the t(9;14)(p13;q32) the t(11;18)(q21;q21) a 6q- chromosome Numerical abberrations involving several chromosomes were also detected. Recurrent aberrations include trisomy 1q, and trisomy 3q Genes involved and Proteins Note The t(9;14)(p13;q32), fuses PAX5 with the IgH gene. PAX5 was shown to code for the BSAP (B-cell specific activator protein). The t(11;18)(q21;q21) is cytogenetically indistinguishable from the classical t(11;18) found in MALT lymphoma, where involvement of the API2- MLT genes was demonstrated.

Waldenstrom macroglobulinemia

CUNEO, Antonio
2001

Abstract

Disease Waldenstrom's macroglobulinemia (corresponding to lymphoplasmacytoid lymphoma / Immunocytoma in the REAL and WHO classification) Phenotype / cell stem origin Stem cell origin: Post-germinal centre IgM-bearing memory B-cell. Phenotype: CD19+; CD20+; CD22+; FMC7+; CD38+; cytoplasmic IgM bright+; CD5-; CD23-; CD10-. Epidemiology It accounts for 1-2% of all nodal lymphomas. The annual incidence falls in the 0,2-0,6% range per 100 000. Clinics Indolent lymphoma characterized by the secretion of a monoclonal IgM protein and by the expansion of the neoplastic clone in the bone marrow, in the lymphoid tissue and in extra-nodal sites. The symptoms derive from tissue infiltration, bone marrow failure and from the presence of the IgM paraprotein (hyperviscosity syndrome, polyneuropathies, AL amyloidosis) Pathology Diffuse proliferation of small lymphocytes, plasmacytoid lymphocytes and plasma cells, infiltrating the bone marrow and the interfollicular areas of the lymph nodes. By definition, this lymphoma subtype lacks the diagnostic features chronic lymphocytic leukemia (CLL), mantle cell lymphoma and follicle centre cell lymphoma. Transformation into high grade lymphoma may occur in a minority (5%) of cases.. Treatment Alkylating agents (chlorambucil), multiagent chemotherapy (vincristine cyclophosphamide, steroid, with or without anthtacyclines); fludarabine, with or without mitoxantrone. Prognosis Median survival exceeds 5 years and there is no plateau in the survival curve, just as in other low-grade lymphomas. Cytogenetics Cytogenetics Morphological There is no chromosome anomaly that is specific for WM. The overall cytogenetic picture is similar to that of marginal zone B-cell lymphoma. Recurrent structural changes include the t(9;14)(p13;q32) the t(11;18)(q21;q21) a 6q- chromosome Numerical abberrations involving several chromosomes were also detected. Recurrent aberrations include trisomy 1q, and trisomy 3q Genes involved and Proteins Note The t(9;14)(p13;q32), fuses PAX5 with the IgH gene. PAX5 was shown to code for the BSAP (B-cell specific activator protein). The t(11;18)(q21;q21) is cytogenetically indistinguishable from the classical t(11;18) found in MALT lymphoma, where involvement of the API2- MLT genes was demonstrated.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11392/1190773
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