Literature DB >> 3876128

Peripheral T cell lymphoma: immunologic and cell-kinetic observations associated with morphological progression.

C D Winberg, K Sheibani, R Krance, H Rappaport.   

Abstract

Peripheral T cell lymphomas (PTCLs) form a morphologically heterogeneous group of non-Hodgkin's lymphomas that are generally considered to have immunophenotypes associated with mature T cells, usually those of helper T cells. We now describe and correlate the clinical, morphological, immunologic, and cell-kinetic findings based on the evaluation of eight tissue samples obtained at various times from a 13-year-old girl with PTCL. The early morphological expressions of this patient's PTCL were those of diffuse mixed-cell lymphoma and focal large-cell lymphoma (LCL) evolving from the histologic picture of an atypical immune response (AIR). These morphological findings were associated with an immature T cell immunophenotype associated with cortical thymocytes--namely, sheep erythrocyte rosette (sER)+, T11+, Leu-2a+, Leu-3a+, HLA-DR+, OKT6-, OKT9+, OKT10+--and with cell-kinetic findings that showed no evidence of aneuploidy and few cells in S phase. Diffuse pleomorphic LCL developed, which was associated with further dedifferentiation of the neoplastic T cells to the immunophenotype sER-, T11+, Leu-2a-, Leu-3a-, HLA-DR+, OKT6-, OKT9+, OKT10- and with cell-kinetic findings that demonstrated a distinct aneuploid population and a dramatic increase in the percentage of cells in the S phase. The immunophenotype of the PTCL at the time of the patient's death was T11-, Leu-2a-, Leu-3a-, HLA-DR+, OKT6-, OKT9+, OKT10-, an immunophenotype indistinguishable from that of a non-B non-T cell lymphoma. The immunologic findings in this case also suggest that an AIR in some cases may represent a prelymphomatous state or may be a morphological expression of PTCL. These observations indicate that PTCLs may be characterized by rapidly changing clinical, morphological, immunologic, and cell kinetic findings which are best evaluated by multidisciplinary studies.

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Year:  1985        PMID: 3876128

Source DB:  PubMed          Journal:  Blood        ISSN: 0006-4971            Impact factor:   22.113


  7 in total

1.  Molecular basis for the aberrant expression of T cell antigens in postthymic T cell malignancies.

Authors:  I J Su; S P Balk; M E Kadin
Journal:  Am J Pathol       Date:  1988-08       Impact factor: 4.307

2.  Expression of growth factor/receptor genes in postthymic T cell malignancies.

Authors:  I J Su; M E Kadin
Journal:  Am J Pathol       Date:  1989-09       Impact factor: 4.307

3.  Relationships among expression, transcription and rearrangement of T-cell receptor beta gene in T-cell lymphomas.

Authors:  K Kasai; T Kameya; M Ono; C Wada; S Kuwao; T Motoori
Journal:  Virchows Arch A Pathol Anat Histopathol       Date:  1990

4.  Clonality of T cell and phenotypically undefined lymphoid neoplasms: the value of genotypic analyses.

Authors:  E Hodges; G N Stacey; W M Howell; D B Jones; J L Smith
Journal:  J Clin Pathol       Date:  1990-07       Impact factor: 3.411

5.  Peripheral T-cell lymphomas. Immunophenotype, lymphokine production, and immunologic functional characteristics of the lymph-node malignant T cells.

Authors:  S Raziuddin; T Malatani; S al-Sedairy; A H al-Saigh
Journal:  Am J Pathol       Date:  1991-11       Impact factor: 4.307

6.  Discordant expression of CD3 and T-cell receptor beta-chain antigens in T-lineage lymphomas.

Authors:  L J Picker; M B Brenner; L M Weiss; S D Smith; R A Warnke
Journal:  Am J Pathol       Date:  1987-12       Impact factor: 4.307

7.  Phenotypic and genotypic heterogeneity of peripheral T-cell lymphoma.

Authors:  J L Smith; D G Haegert; E Hodges; G N Stacey; W M Howell; D H Wright; D B Jones
Journal:  Br J Cancer       Date:  1988-12       Impact factor: 7.640

  7 in total

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