B-LINEAGE PROLYMPHOCYTIC LEUKEMIA AS A DISTINCT CLINICOPATHOLOGIC ENTITY
- 1 January 1980
- journal article
- research article
- Vol. 99 (2) , 399-412
Abstract
There is a controversy over whether PLL [prolymphocytic leukemia] represents one disorder or a heterogeneous group of disorders. Three patients who satisfied Galton''s original diagnostic criteria for PLL were examined by pathologic and immunologic methods. The spleens of these patients showed distinctive pseudonodular pathologic features. The malignant prolymphocytes were characterized as B[bone marrow-derived]-lineage by the presence of surface Ig[immunoglobulin]M and IgD, the expression of HLA-DR antigen, the absence of E[erythrocyte]-rosette formation and the absence of natural killer cell activity. The existence of B-lineage prolymphocytic leukemia is affirmed as a distinct entity with unique pathologic, clinical and immunobiologic characteristics.This publication has 31 references indexed in Scilit:
- CHRONIC LYMPHOCYTIC LEUKÆMIA OF T-CELL ORIGIN IMMUNOLOGICAL AND CLINICAL EVALUATION IN ELEVEN PATIENTSThe Lancet, 1975
- Substitute for Benzidine in Myeloperoxidase StainsAmerican Journal of Clinical Pathology, 1975
- Needle‐Like Crystals in Plasma Cells in a Patient with a Plasma Cell Proliferative DisorderScandinavian Journal of Haematology, 1975
- Nodlar lymphoma: An ultrastructural study of its relationship to germinal genters and a correlation of light and electron microscopic findingsCancer, 1975
- Prolymphocytic LeukaemiaBritish Journal of Haematology, 1974
- PROLYMPHOCYTIC LEUKÆMIA OF B AND T CELL TYPEThe Lancet, 1973
- Intracellular IgA immunoglobulin crystals in chronic lymphocytic leukaemia.1973
- Subdivision of classical varieties of acute leukemia. Correlation with prognosis and cure expectancy.1971
- [Chronic lymphoid leukemia with cristals with non-excreted intracellular monoclonal macroglobulin].1971
- Cytochemical Identification of Monocytes and GranulocytesAmerican Journal of Clinical Pathology, 1971