S100-Positive, T-Cell Chronic Lymphoproliferative Disease: An Aggressive Disorder of an Uncommon T-Cell Subset

• Published in: Blood 1991-10, Vol.78 (7), p.1803-1813
• Main Authors: Hanson, Curtis A., Bockenstedt, Paula L., Schnitzer, Bertram, Fox, David A., Kueck, Brian, Braun, Daniel K.
• Format: Article
• Language: English
• Subjects: Adult; AIDS/HIV; Biological and medical sciences; Blotting, Northern; Blotting, Southern; Bone Marrow - pathology; Chronic Disease; Cytotoxicity, Immunologic; Female; Gene Rearrangement, T-Lymphocyte; Hematologic and hematopoietic diseases; Humans; Immunophenotyping; Liver - chemistry; Liver - pathology; Lymph Nodes - chemistry; Lymph Nodes - pathology; Lymphoproliferative Disorders - genetics; Lymphoproliferative Disorders - pathology; Lymphoproliferative Disorders - physiopathology; Male; Medical sciences; Microscopy, Electron; Middle Aged; S100 Proteins - analysis; Spleen - chemistry; Spleen - pathology; T-Lymphocytes - immunology; T-Lymphocytes - ultrastructure
• ISSN: 0006-4971; 1528-0020
• DOI: 10.1182/blood.V78.7.1803.1803

S100-positive T lymphocytes account for less than 3% of peripheral blood T cells. Rare cases of S100-positive T-cell lymphoma have been previously described. We report four such cases of S100-positive T-cell chronic lymphoproliferative disease. In all cases, hepatosplenomegaly was observed, without prominent lymphadenopathy. Central nervous system (CNS) involvement by the leukemic cells was suggested in three cases by physical symptoms and confirmed in two cases by cerebrospinal fluid studies. Despite treatment, three patients died at 3, 6, and 8 months after diagnosis. Although there was a leukemic presentation, only minimal bone marrow infiltration was evident. Splenectomy showed red pulp infiltration. Liver and lymph node biopsies showed sinusoidal leukemic involvement. In all cases, the leukemic cells expressed mature T-cell- and natural killer cell-associated antigens. Cytoplasmic S100 was detected in the leukemic cells in the blood, spleen, liver, and lymph node. Southern blot studies in two cases showed T-β, T-γ, and T-δ gene rearrangements. RNA Northern blots showed T-α and T-β chain transcripts with no T-γ or T-δ RNA identified. Southern blot analysis showed no hybridization to probes specific for Epstein-Barr virus, cytomegalovirus, human immunodeficiency virus-1, or human T-cell lymphotropic virus type-1. These findings show that S100-positive T-cell chronic lymphoproliferative disorder is an aggressive, extramedullarybased disease frequently associated with CNS involvement and characterized by short survivals.