Perkins and Friedberg (pp 341–348) Figure 2.
Perkins and Friedberg (pp 341–348) Figure 2. A. Low-power H&E-stained section of a lymph node involved with Burkitt lymphoma (BL) from an 82-year-old man. Note the uniform appearance of the cells, the diffuse pattern of growth, and the nuclear debris from apoptotic cells, mostly contained within the cytoplasm of pale-staining tingible-body macrophages. B. Cytology of bone marrow cells, as seen on Wright-Giemsa–stained aspirates and touch preps. Note the high nuclear-to-cytoplasmic ratio, moderately abundant dark blue cytoplasm with occasional vacuoles, and nucleus with finely granular chromatin and multiple nucleoli. C. Identification of MYC translocation by FISH analysis using “MYC break-apart probes. When together, as in a normal chromosome, the two probes are located in close proximity and give a composite yellow color, while the probes are distinct when translocation occurs (Taken with permission from Hecht and Aster39). D. Composite figure from paper by Hummel et al.6 depicting the results of gene array studies, karyotype and FISH analyses. Top, bar graph depicting the karyotypic complexity of each case. The mBL Index section depicts a heat map of the 58 mBL signature genes; blue is low expression, while yellow is high expression. IG-myc translocations are in bright green; non-IG-myc fusions are in dark green, and myc-absent are in red. At bottom, histologic diagnosis: bright green, BL; dark green, atypical BL; red, diffuse large B-cell lymphoma (DLBCL); grey, unclassifiable mature aggressive B-cell lymphoma.

A. Low-power H&E-stained section of a lymph node involved with Burkitt lymphoma (BL) from an 82-year-old man. Note the uniform appearance of the cells, the diffuse pattern of growth, and the nuclear debris from apoptotic cells, mostly contained within the cytoplasm of pale-staining tingible-body macrophages. B. Cytology of bone marrow cells, as seen on Wright-Giemsa–stained aspirates and touch preps. Note the high nuclear-to-cytoplasmic ratio, moderately abundant dark blue cytoplasm with occasional vacuoles, and nucleus with finely granular chromatin and multiple nucleoli. C. Identification of MYC translocation by FISH analysis using “MYC break-apart probes. When together, as in a normal chromosome, the two probes are located in close proximity and give a composite yellow color, while the probes are distinct when translocation occurs (Taken with permission from Hecht and Aster39). D. Composite figure from paper by Hummel et al.6 depicting the results of gene array studies, karyotype and FISH analyses. Top, bar graph depicting the karyotypic complexity of each case. The mBL Index section depicts a heat map of the 58 mBL signature genes; blue is low expression, while yellow is high expression. IG-myc translocations are in bright green; non-IG-myc fusions are in dark green, and myc-absent are in red. At bottom, histologic diagnosis: bright green, BL; dark green, atypical BL; red, diffuse large B-cell lymphoma (DLBCL); grey, unclassifiable mature aggressive B-cell lymphoma.

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