Splenic marginal-zone lymphoma (SMZL, splenic lymphoma with villous lymphocytes)

Definition

There is prominent splenic involvement with minimal involvement of the liver, blood and bone marrow. Small lymphocytes replace the splenic white pulp germinal centres, efface the follicle mantle and merge with a peripheral (marginal) zone of larger cells. Splenic hilar nodes and bone marrow are often involved. Villous lymphocytes may be found in the peripheral blood.

Synonyms

Epidemiology

Rare, less than 1% of all lymphoid neoplasms, but accounts for many CD5-negative chronic lymphoid leukaemias.

Macroscopic appearances

Splenic weight may be mildly or massively increased. The cut surface shows a multimicronodular pattern, with nodules less than 0.5 cm in diameter. Splenic hilar lymph nodes are commonly enlarged. The liver may be involved but usually not peripheral lymph nodes.

Histopathology

The white pulp shows enlargement of follicles due to a broad clear marginal zone caused by lymphomatous infiltration. These infiltrating cells are medium sized and resemble monocytoid B cells; they have abundant pale cytoplasm, clear cell borders and nuclei with are oval or slightly irregular. Larger immunoblasts / centroblasts are seen but usually constitute a small proportion of the population. Follicles may be reactive in appearance or show a Castleman-like onion-bulb pattern. In some cases, there is a lymphoplasmacytic component is present involving the marginal zones, germinal centres as well as infiltrating the mantle zones. The red pulp is always involved with both small nodules of the larger cells and sheets of small lymphocytes. epithelioid histiocytes may be present. Plasmacytic differentiation may occur, rarely with clusters of plasma cell in the centres of the white pulp follicles. There may be a focal pseudo-angiomatous pattern, as is seen in hairy cell leukaemia.

The lymph nodes of the splenic hilum are infiltrated by monocytoid cells, varying from a perifollicular arrangement (although the formation of a marginal zone is less distinct) to homogenisation. If there is a plasmacytoid component in the spleen, this is also seen in the lymph nodes. Sinuses are dilated.

Liver and bone marrow involvement are common1. The marrow infiltrate is nodular and interstitial. Villous lymphocyte leukaemia appears to represent a leukaemic phase of splenic marginal zone lymphoma.

One case of SMZL associated with micronodular T-cell rich B-cell lymphoma in the red pulp has been reported6.

Immunohistochemistry

 

splenic marginal zone lymphoma

SMZL transformed to large B-cell lymphoma

CD3

negative

negative

CD5

usually negative

CD10

negative

usually negative

CD11c†

variable

 

CD19†

positive

 

CD20

positive

positive

CD23†

usually negative

negative

CD25

variable

 

CD38

variable

variable

CD43

negative

usually negative

CD45RA

positive

 

CD79a

positive

 

CD103

negative

 

bcl-2

positive

positive

bcl-6

negative

usually positive

cyclin-D1

negative

negative

DBA44

negative

 

SIg

positive

 

SIgD

variable

 

SIgM

may be positive

 

†: fresh frozen tissue only

Monotypic immunoglobulins are demonstrable in those cases with plasmacytoid differentiation1. CD3, CD5 and CD43 stain only the T cell component, which is present in the red pulp and in periarteriolar sheets, but may sometimes infiltrate the marginal zones in large numbers1.

Cytogenetics

The most common abnormalities in splenic lymphoma with villous lymphocytes involve 7q, usually at q21-22. This is immediately upstream of the CDK6 gene, which controls entry to the S phase of the cell cycle, suggesting that deregulation of CDK6 contributes to the pathogenesis of SLVL5.

Differential diagnosis

Prognosis

The clinical course is indolent. About 10% of cases undergo transformation to large B-cell lymphoma3.

References

World Health Organization Classification of Tumours, Tumours of the haematopoietic and lymphoid tissues, IARC Press 2001.

1 J-P D van Huyen et al. Splenic marginal zone lymphoma with or without plasmacytic differentiation. Am J Surg Pathol 2000;24:1581-1592.

2 Wotherspoon AC, Hasserjian RP. Immunophenotyping in the differential diagnosis of histologically low grade B cell lymphomas. Current Diagnostic Pathology 2000;6:55-63.

3 Camacho, F. I., Mollejo, M., Mateo, M. S. Progression to large B-cell lymphoma in splenic marginal zone lymphoma: a description of a series of 12 cases. Am J Surg Pathol 2001;25:1268-1276.

4 Piris, M. A., Mollejo, M., Campo, E., Menarguez, J., Flores, T., Isaacson, P. G. A marginal zone pattern may be found in different varieties of non- Hodgkin's lymphoma: the morphology and immunohistology of splenic involvement by B-cell lymphomas simulating splenic marginal zone lymphoma. Histopathology 1998;33:230-9.

5 Leoncini, L., Lazzi, S., Bellan, C. and Tosi, P. Cell kinetics and cell cycle regulation in lymphomas. J Clin Pathol 2002;55:648-55.

6 Wang SA, Olson N, Zukerberg L, et al. Splenic Marginal Zone Lymphoma With Micronodular T-Cell Rich B-Cell Lymphoma. Am J Surg Pathol 2006; 30:128-132

This page last revised 28.1.2006.

©SMUHT/PW Bishop