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Molecular Cytogenetic Analyses of Immunoglobulin Loci in Nodular Lymphocyte Predominant Hodgkin's Lymphoma Reveal a Recurrent IGH-BCL6 Juxtaposition 

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Presentation on theme: "Molecular Cytogenetic Analyses of Immunoglobulin Loci in Nodular Lymphocyte Predominant Hodgkin's Lymphoma Reveal a Recurrent IGH-BCL6 Juxtaposition "— Presentation transcript:

1 Molecular Cytogenetic Analyses of Immunoglobulin Loci in Nodular Lymphocyte Predominant Hodgkin's Lymphoma Reveal a Recurrent IGH-BCL6 Juxtaposition  Christoph Renné, José Ignacio Martín-Subero, Martin-Leo Hansmann, Reiner Siebert  The Journal of Molecular Diagnostics  Volume 7, Issue 3, Pages (August 2005) DOI: /S (10) Copyright © 2005 American Society for Investigative Pathology and Association for Molecular Pathology Terms and Conditions

2 Figure 1 A: Combined immunophenotyping and FISH for the detection of CD20 and breakpoints in the IGH locus in case NP19. The CD20-positive large cell (blue) displays a split of the signals flanking the IGH locus indicating the presence of a translocation. The CD20 antigen detected with Alexa-594 (red fluorescence) is displayed in blue. B: Triple-color FISH assay for the detection of the t(3;14)(q27;q32) translocation juxtaposing the BCL6 and IGH loci (false color display) in case NP20. This probe set was made of the LSI IGH flanking probe (IGH telomeric in green and IGH centromeric in red) combined with a BCL6-spanning probe labeled in DEAC (pale blue signals). The small nucleus on the right displays the regular signal constellation: two red/green co-localizations indicating intact IGH gene and two pale blue signals pointing to intact BCL6 alleles. The large nucleus on the left shows multiple split of green and red signals indicating a breakpoint in the IGH locus. Disrupted red and green signals co-localize with pale blue BCL6 signals pointing to a t(3;14)(q27;q32) translocation involving the BCL6 and IGH loci as well as the presence of several derivative chromosomes. This signal pattern was found recurrently in this case. The Journal of Molecular Diagnostics 2005 7, DOI: ( /S (10) ) Copyright © 2005 American Society for Investigative Pathology and Association for Molecular Pathology Terms and Conditions


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