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.
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.
|
splenic marginal zone lymphoma |
SMZL transformed to large B-cell lymphoma |
negative: 0/123 |
negative: 0/123 |
|
usually negative: 2/73 |
variable: 3/63 |
|
negative: 0/93 |
usually negative: 1/63 |
|
variable |
|
|
positive |
|
|
positive : 12/123 |
positive : 12/123 |
|
usually negative : 1/113 |
negative : 1/73 |
|
variable |
|
|
variable : 5/83 |
variable : 3/73 |
|
negative : 0/83 |
usually negative: 2/73 |
|
positive |
|
|
positive |
||
CD103 |
negative |
|
positive : 12/123 |
positive : 8/93 |
|
negative : 0/93 |
usually positive : 6/83 |
|
negative : 0/9 (scattered cells positive in one case)3 |
negative : 0/7 (scattered cells positive in one case)3 |
|
negative |
|
|
SIg |
positive |
|
SIgD |
variable: positive in 15 of 24 cases1 |
|
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
A multimicronodular pattern may be observed in a range of small B-cell lymphomas, including follicular lymphoma and mantle cell lymphoma4, with the exception of hairy cell leukaemia.
lymphoplasmacytoid differentiation may cause a resemblance to lymphoplasmacytic lymphoma.
Prognosis
References
World Health Organization Classification of Tumours, Tumours of the haematopoietic and lymphoid tissues, IARC Press 2001.
2 Wotherspoon AC, Hasserjian RP. Immunophenotyping in the differential diagnosis of histologically low grade B cell lymphomas. Current Diagnostic Pathology 2000;6:55-63.
This page last revised 28.1.2006.
©SMUHT/PW Bishop