Literature DB >> 2169708

The value of immunophenotyping on paraffin sections in the identification of T-cell rich B-cell large-cell lymphomas: lineage confirmed by JH rearrangement.

B M Osborne1, J J Butler, W C Pugh.   

Abstract

Immunophenotyping of lymphomas using paraffin-embedded lymphoid tissue, not previously distorted by frozen section, is useful in identifying the large neoplastic B cells that may be in the minority in T-cell rich B-cell lymphoma (TCRBCL). Even in cases in which frozen tissue sections are available, the improved morphology in unfrozen sections allows the proper classification of these lymphomas as large cell and identifies their B-cell lineage, which is important for clinical therapeutic studies. Seven cases initially believed to be diffuse mixed cell lymphoma of possible peripheral T-cell lineage showed the large cells to be immunoreactive with L-26 (pan B-cell marker) with the majority of smaller lymphocytes immunoreactive for UCHL-1 and Leu-22 (pan T-cell markers). K/lambda immunostaining on frozen sections was equivocal. In these cases, the diagnosis of large-cell lymphoma of B-cell lineage was confirmed by detection of immunoglobulin heavy- (all seven cases) and light- (six of seven cases) chain gene rearrangements, with germ-line configuration of the T-cell receptor beta-chain gene (all cases). Some cases of TCRBCL may not show detectable rearrangement of the immunoglobulin genes because of the low concentration of neoplastic cells in the samples submitted. The presence of rearrangements in these seven cases, however, supports the diagnosis of TCRBCL based on paraffin immunophenotyping when frozen tissue is not available or when molecular studies are not feasible. Although these seven cases are classified as large-cell lymphoma, an intermediate-grade lymphoma, the influence of the reactive T-cell population on the clinical behavior will require follow-up studies.

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Year:  1990        PMID: 2169708     DOI: 10.1097/00000478-199010000-00006

Source DB:  PubMed          Journal:  Am J Surg Pathol        ISSN: 0147-5185            Impact factor:   6.394


  7 in total

1.  Morphological variability of tumour cells in T-cell-rich B-cell lymphoma. A histopathological study of 14 cases.

Authors:  S Camilleri-Bröet; T Molina; J Audouin; A L Tourneau; J Diebold
Journal:  Virchows Arch       Date:  1996-11       Impact factor: 4.064

Review 2.  T cell/histiocyte-rich large B-cell lymphoma: an update on its biology and classification.

Authors:  Thomas Tousseyn; Christiane De Wolf-Peeters
Journal:  Virchows Arch       Date:  2011-11-12       Impact factor: 4.064

3.  Primary T-cell rich B-cell lymphoma of the common bile duct.

Authors:  J P Brouland; J Molimard; J Nemeth; P Valleur; A Galian
Journal:  Virchows Arch A Pathol Anat Histopathol       Date:  1993

4.  Histiocytic and t-cell rich b-cell lymphoma (TCRBCL) of the stomach.

Authors:  J Tóth; G Elek
Journal:  Pathol Oncol Res       Date:  1997-09       Impact factor: 3.201

5.  Leu 7 (CD57) reactivity distinguishes nodular lymphocyte predominance Hodgkin's disease from nodular sclerosing Hodgkin's disease, T-cell-rich B-cell lymphoma and follicular lymphoma.

Authors:  O W Kamel; A B Gelb; R B Shibuya; R A Warnke
Journal:  Am J Pathol       Date:  1993-02       Impact factor: 4.307

6.  Interleukin-4 may contribute to the abundant T-cell reaction and paucity of neoplastic B cells in T-cell-rich B-cell lymphomas.

Authors:  W R Macon; J B Cousar; J A Waldron; S M Hsu
Journal:  Am J Pathol       Date:  1992-11       Impact factor: 4.307

7.  Primary cutaneous B-cell lymphoma with abundant reactive gamma/delta T-cells within the skin lesion and peripheral blood.

Authors:  Mitsuaki Ishida; Muneo Iwai; Keiko Yoshida; Akiko Kagotani; Hidetoshi Okabe
Journal:  Int J Clin Exp Pathol       Date:  2014-02-15
  7 in total

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