2017
DOI: 10.1080/10428194.2017.1330469
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Burkitt lymphoma and diffuse large B-cell lymphoma: a unique case of a composite lymphoma of different clonal origin

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Cited by 2 publications
(2 citation statements)
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“…Considering that categorization of BLL-11q as a variant of BL, DLBCL or another distinct form of large B-cell lymphoma remains uncertain, the present case is significant in keeping with previous reports in terms of supporting the perspective that BLL-11q is a distinct entity from BL. 8,12 This sheds light on the lymphomagenesis of CL that may originate from non-immunoglobulin gene-rearranged common progenitor cells.…”
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confidence: 95%
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“…Considering that categorization of BLL-11q as a variant of BL, DLBCL or another distinct form of large B-cell lymphoma remains uncertain, the present case is significant in keeping with previous reports in terms of supporting the perspective that BLL-11q is a distinct entity from BL. 8,12 This sheds light on the lymphomagenesis of CL that may originate from non-immunoglobulin gene-rearranged common progenitor cells.…”
mentioning
confidence: 95%
“…Horing et al reported CL of DLBCL and BL in ileocecal area which was similar site with our case exhibiting two separate clonal population on IgH gene rearrangement analysis. 8 Considering that genetic alteration of the case was not fully examined in detail and several cases of BLL-11q have been morphologically indistinguishable from DLBCL, the prior case of CL at the same site may provide a clue for understanding pathogenesis of large B-cell lymphoma. 9,10 Although BLL-11q has been described to resemble BL on morphological, immunophenotypic and gene-expression levels, it lacks MYC rearrangements and has a chromosome 11q alteration characterized by proximal gains and telomeric losses: specifically, interstitial gains including a minimal region of gain in 11q23.2-23.3 and losses of 11q24.1-qter.…”
mentioning
confidence: 99%