Literature DB >> 1615915

Positive immunoglobulin gene rearrangement study by the polymerase chain reaction in a colonic adenocarcinoma.

F C Ling1, C E Clarke, D Lillicrap.   

Abstract

The detection of clonal rearrangements of the immunoglobulin heavy chain gene by the polymerase chain reaction provides a rapid method to differentiate monoclonal from polyclonal B-lymphocyte proliferations. It has been shown to be highly specific and so far, no false-positive results have been described. A case of a poorly differentiated colonic adenocarcinoma that showed a "false positive" clonal immunoglobulin heavy chain gene rearrangement by the polymerase chain reaction technique is reported. DNA contamination was unlikely because of the strict adherence to the laboratory polymerase chain reaction protocol and also the repeated demonstration of the same amplified band in a separate experiment using DNA extracted from another piece of tumor tissue. The apparent monoclonal immunoglobulin heavy chain gene rearrangement in the first polymerase chain reaction may be related to a combination of the paucity of lymphoid cells in the tissue sample and the presence within this small number of lymphocytes of a clonal reactive cell population. It is, therefore, important to correlate the routine microscopic and immunohistochemical findings in the interpretation of polymerase chain reaction results, especially when working with nonlymphoid tumors and lymphocyte-poor lesions.

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Year:  1992        PMID: 1615915     DOI: 10.1093/ajcp/98.1.116

Source DB:  PubMed          Journal:  Am J Clin Pathol        ISSN: 0002-9173            Impact factor:   2.493


  7 in total

1.  PCR analysis of the immunoglobulin heavy chain gene in polyclonal processes can yield pseudoclonal bands as an artifact of low B cell number.

Authors:  K S Elenitoba-Johnson; S D Bohling; R S Mitchell; M S Brown; R S Robetorye
Journal:  J Mol Diagn       Date:  2000-05       Impact factor: 5.568

2.  Analysis of T-cell clonality using laser capture microdissection and high-resolution microcapillary electrophoresis.

Authors:  Evgeny Yakirevich; Cynthia L Jackson; Patricia A Meitner; Dolores MacKenzie; Rose Tavares; Leslie Robinson-Bostom; Ronald A DeLellis; Murray B Resnick
Journal:  J Mol Diagn       Date:  2007-07-09       Impact factor: 5.568

3.  Assessment of clonality in lymphoid proliferations.

Authors:  L M Weiss; D V Spagnolo
Journal:  Am J Pathol       Date:  1993-06       Impact factor: 4.307

4.  Sensitivity of PCR in detecting monoclonal B cell proliferations.

Authors:  F C Ling; C E Clarke; W E Corbett; D P Lillicrap
Journal:  J Clin Pathol       Date:  1993-07       Impact factor: 3.411

5.  Detection of clonal B cells in microdissected reactive lymphoproliferations: possible diagnostic pitfalls in PCR analysis of immunoglobulin heavy chain gene rearrangement.

Authors:  X G Zhou; K Sandvej; N Gregersen; S J Hamilton-Dutoit
Journal:  Mol Pathol       Date:  1999-04

6.  Identification of monoclonal B-cell populations by rapid cycle polymerase chain reaction. A practical screening method for the detection of immunoglobulin gene rearrangements.

Authors:  G H Segal; C T Wittwer; A J Fishleder; M H Stoler; R R Tubbs; C R Kjeldsberg
Journal:  Am J Pathol       Date:  1992-12       Impact factor: 4.307

7.  PCR-based assays for the detection of monoclonality in non-Hodgkin's lymphoma: application to formalin-fixed, paraffin-embedded tissue and decalcified bone marrow samples.

Authors:  G Weirich; A Funk; I Hoepner; U Heider; S Noll; B Pütz; C Fellbaum; H Höfler
Journal:  J Mol Med (Berl)       Date:  1995-05       Impact factor: 4.599

  7 in total

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