A mixture of small lymphocytes, plasmacytoid lymphocytes, and plasma cells is characteristic of LPL; however, this is not specific for LPL, since other low-grade B-cell lymphomas can present with plasma cell differentiation especially marginal zone lymphoma.
This immunophenotype is typical for LPL. The most common heavy chain isotype expressed and secreted by LPL is IgM.
Hyperviscosity occurs in up to 30% of LPL patients and the syndrome defined by hypervicosity is known as Waldenstrom macroglobulinemia.
This immunophenotype is characteristic for chronic lymphocytic leukemia/small lymphocytic lymphoma (CLL/SLL) not LPL.
Admixture of increased mast cells is often seen in the bone marrow of LPL patients.