The bone marrow is almost always involved. There is hepatomegaly, lymphadenopathy or splenomegaly in 15-20% of patients. Hyperviscocity syndrome occurs in 15-20% of patients.
Where there are extramedullary tumour deposits, these vary in moth morphology and immunophenotype. In a study of 44 patients with extramedullary disease, the following were reported1:
Low grade lymphoplasmacytic lymphoma, CD5-: nodal = 28, extranodal = 11. Lymphoplasmacytic (many plasmacytoid lymphocytes and more mature plasma cells) = 21, lymphoplasmacytoid (mainly small mature lymphocytes with a variable number of plamacytoid lymphocytes and rare plasma cells) = 18. Six cases had marked interfollicular infiltration, reactive germinal centres and monocytoid B-cells resembling MZBCL. One showed nodular expansion of follicles, simulating follicular lymphoma. One contained numerous epithelioid histiocytes, simulating LPHD.
Aggressive lymphoma associated with concurrent lymphoplasmacytic lymphoma in the bone marrow: nodal = 4, extranodal = 2. DLBCL = 4, polymorphous lymphoplasmacytic lymphoma = 1, composite classical HD = 1.
Variant lymphoplasmacytic lymphoma, CD5+: nodal = 1, extranodal = 1. In one case the bone marrow infiltrate was also CD5+. In the other, the bone marrow infiltrate was CD5-.
Other non-Hodgkin lymphomas: nodal = 3, extranodal = 1. SLL/CLL = 2, MCL (cyclin D1+, t(11;14)) = 1, cutaneous FL (bcl-6+) = 1.
References
6Van Huyen, J. P., T. Molina, et al. (2000). "Splenic marginal zone lymphoma with or without plasmacytic differentiation." Am J Surg Pathol 24(12): 1581-92.
This page last revised 11.9.2003.
©SMUHT/PW Bishop