Definition
There is a sustained increase in the number of large granular lymphocytes in the peripheral blood.
Epidemiology
Accounts for 2-3% of cases of small lymphocytic leukaemia
Clinical features
60% of patients are symptomatic at presentation. Moderate splenomegaly1, rheumatoid arthritis1, circulating immune complexes and hypergammaglobulinaemia are common. Lymphadenopathy is uncommon1. Severe neutropenia is common1. Severe anaemia due to red cell hypoplasia may occur. The lymphocytosis usually exceeds 5.109/l.
Histopathology
The large granular lymphocytes in blood and bone marrow have abundant cytoplasm with azurophilic granules. The bone marrow involvement is often interstitial, rarely nodular.
The spleen, which may weigh up to 1.8 kg, shows preservation of the architecture, with a lymphocytic infiltrate within the red pulp. Neoplastic cells infiltrate the walls of blood vessels. The white pulp is preserved, with the marginal zone demarcated by granzyme-negative lymphocytes. Germinal centres are present and may be prominent. In one cases, non-caseating granulomas were observed1.
Immunohistochemistry
positive |
||
positive1 |
||
variable |
||
positive |
||
variable |
||
variable, more often in common type |
||
usually positive, 5/51 |
||
Perforin |
5/51 |
|
Granzyme B |
3/41 |
|
negative1 |
||
MIB1 |
low expression1 |
|
The following variants exist:
|
common variant |
rare variants |
||
TCRab |
positive |
positive |
positive |
negative |
TCRgd |
negative |
negative |
negative |
positive |
negative1 |
positive |
positive |
not defined |
|
positive1 |
negative |
positive |
not defined |
Differential diagnosis
Cases resembling T-LGL but with an NK immunophenotype (CD3-, TCRab- and gd-) are classified with the NK disorders.
Management
Splenectomy is therapeutic in cases with hypersplenism1.
References
0 World Health Organization Classification of Tumours, Tumours of the haematopoietic and lymphoid tissues, IARC Press 2001.
This page last revised 24.9.2005.
©SMUHT/PW Bishop