Modifications of lymphocyte subsets in autoimmune thrombocytopenic purpura patients submitted to splenectomy.

1. Matutes E, Keeling DM, Newland AC, et al. Sezary celllike leukemia: a distinct type of mature T cell malignancy. Leukemia 1990; 4:262-6. 2. Pawson R, Matutes E, Brito-Babapulle V, et al. Sezary cell leukaemia: a distintc T cell disorder or a variant form of T prolymphocytic leukaemia? Leukemia 1997; 11:1009-13. 3. Garand R, Goasguen J, Brizard A, et al. Indolent course as a relatively frequent presentation in T-prolymphocytic leukaemia. Groupe Francais d’Hematologie Cellulaire. Br J Haematol 1998;103:488-94. 4. Harris NL, Jaffe ES, Diebold J, et al. World Health Organization classification of neoplastic diseases of the hematopoietic and lymphoid tissues:report of the Clinical Advisory Committee meeting-Airlie House, Virginia, November 1997. J Clin Oncol 1999; 17: 3835-49. 5. Matutes E, Brito-Babapulle V, Swansbury J, et al. Clinical and laboratory features of 78 cases of T-prolymphocytic leukemia. Blood 1991; 78:3269-74. 6. Huhn D, Thiel E, Rodt H, Schlimok G, Theml H, Rieber P. Subtypes of t-cell chronic lymphatic leukemia. Cancer 1983; 51:1434-47. 7. Brito-Babapulle V, Pomfret M, Matutes E, Catovsky D. Cytogenetic studies on prolymphocytic leukemia. II. T-cell prolymphocytic leukemia. Blood 1987; 70:92631. 8. Brito-Babapulle V, Catovsky D. Inversions and tandem translocations involving chromosome 14q11 and 14q32 in T-prolymphocytic leukemia and T-cell leukemias in patients with ataxia telangiectasia. Cancer Genet Cytogen 1991; 55:1-9. 9. Maljaei SH, Brito-Babapulle V, Hiorns LR, Catovsky D. Abnormalities of chromosomes 8, 11, 14, and X in Tprolymphocytic leukemia studied by fluorescence in situ hybridization. Cancer Genet Cytogen 1998; 103: 110-6. 10. Mossafa H, Brizard A, Huret JL, et al. Trisomy 8q due to i(8q) or der(8) t(8;8) is a frequent lesion in T-prolymphocytic leukaemia: four new cases and a review of the literature. Br J Haematol 1994; 86:780-5.