Literature DB >> 11144922

PCR analysis of immunoglobulin heavy chain (IgH) and TcR-gamma chain gene rearrangements in the diagnosis of lymphoproliferative disorders: results of a study of 525 cases.

C Thériault1, S Galoin, S Valmary, J Selves, L Lamant, D Roda, F Rigal-Huguet, P Brousset, G Delsol, T Al Saati.   

Abstract

This report summarizes a cumulative 4-year experience in polymerase chain reaction (PCR) analysis of immunoglobin heavy chain (IgH) and TcR-gamma chain gene rearrangements in 525 cases of lymphoproliferative disorders. Because the sensitivity of the PCR methodology was found to be tissue dependent, in the study of the presence of clonal cell population in tissues containing a small number of polyclonal lymphocytes, such as skin and gastrointestinal biopsy specimens, we used the multiple-PCR run approach. In this latter methodology, we repeat the PCR reaction from the same sample at least three times to confirm the reproducibility of the results. In the study of 273 cases of B- or T-cell lymphomas with characteristic immunomorphological and clinical features, a clonal IgH or TcR-gamma chain gene rearrangement was detected in approximately 80% of cases. A clonal rearrangement involving both IgH and TcR-gamma chain genes was found in 10% of cases of both B-cell and T-cell lymphomas. The study of 167 cases of nonneoplastic lymphoid tissue samples showed the presence of clonally rearranged cell populations for IgH or TcR-gamma genes in 3 and 9% of cases, respectively. We also applied PCR for the study of 85 cases of lymphoproliferations with no definite diagnosis (i.e., benign versus malignant) after immunomorphological analysis. In 65 cases (76%), the correlation of immunomorphological features with the presence (48 cases) or the absence (17 cases) of clonal lymphoid cell populations led to a definite diagnosis. In almost all these cases, the final diagnosis was found to be in agreement with the clinical course. In the 20 remaining cases (24%), no definite diagnosis could be made. We also assessed the value of PCR in detecting bcl-2/J(H) gene rearrangement as an additional clonal marker in the diagnosis of follicular lymphoma. Bcl-2/J(H) rearrangement and/or IgH gene rearrangement was found in approximately 85% (71/85) of follicular lymphoma cases studied.

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Year:  2000        PMID: 11144922     DOI: 10.1038/modpathol.3880232

Source DB:  PubMed          Journal:  Mod Pathol        ISSN: 0893-3952            Impact factor:   7.842


  32 in total

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4.  Consensus JH gene probes with conjugated 3'-minor groove binder for monitoring minimal residual disease in acute lymphoblastic leukemia.

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5.  Comparative investigations of T cell receptor gamma gene rearrangements in frozen and formalin-fixed paraffin wax-embedded tissues by capillary electrophoresis.

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6.  Primary bone marrow T-cell anaplastic large cell lymphoma with triple M gradient.

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7.  Comparison of BIOMED-2 versus laboratory-developed polymerase chain reaction assays for detecting T-cell receptor-gamma gene rearrangements.

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Journal:  J Mol Diagn       Date:  2010-03       Impact factor: 5.568

8.  Consensus primers for detecting monoclonal immunoglobulin heavy chain rearrangement in B cell lymphomas.

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9.  Extranodal marginal zone lymphoma of the dura mater with IgH/MALT1 translocation and review of literature.

Authors:  Sharathkumar Bhagavathi; Timothy C Greiner; Syed A Kazmi; Kai Fu; Warren G Sanger; Wing C Chan
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10.  Primary NK/T cell lymphoma nasal type of the stomach with skin involvement: a case report.

Authors:  Sebastian Kobold; Hartmut Merz; Markus Tiemann; Carolina Mahuad; Carsten Bokemeyer; Irmtraut Koop; Walter Fiedler
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