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B-cell acute lymphoblastic leukemia as a secondary malignancy following diffuse large B-cell lymphoma

Secondary acute lymphoblastic leukemia (ALL) is a rare disease that has not been well characterized compared with secondary myelodysplastic syndrome or secondary acute myeloid leukemia. We present a report of two patients who developed ALL following complete remission of diffuse large B-cell lymphom...

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Autores principales: Gaut, Daria, Bejjani, Anthony, Sasine, Joshua, Schiller, Gary
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PAGEPress Publications, Pavia, Italy 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6589539/
https://www.ncbi.nlm.nih.gov/pubmed/31285810
http://dx.doi.org/10.4081/hr.2019.8100
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author Gaut, Daria
Bejjani, Anthony
Sasine, Joshua
Schiller, Gary
author_facet Gaut, Daria
Bejjani, Anthony
Sasine, Joshua
Schiller, Gary
author_sort Gaut, Daria
collection PubMed
description Secondary acute lymphoblastic leukemia (ALL) is a rare disease that has not been well characterized compared with secondary myelodysplastic syndrome or secondary acute myeloid leukemia. We present a report of two patients who developed ALL following complete remission of diffuse large B-cell lymphoma (DLBCL). The first case is more consistent with a therapy- related ALL as a PCR analysis of bone marrow aspirate revealed a distinct clone and the mixed-lineage leukemia gene rearrangement, commonly associated with exposure to topoisomerase II inhibitors. The second case is more consistent with clonal evolution given positive MYC and BCL2 fusion signals in the original diagnosis of DLBCL and the secondary ALL.
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spelling pubmed-65895392019-07-08 B-cell acute lymphoblastic leukemia as a secondary malignancy following diffuse large B-cell lymphoma Gaut, Daria Bejjani, Anthony Sasine, Joshua Schiller, Gary Hematol Rep Case Report Secondary acute lymphoblastic leukemia (ALL) is a rare disease that has not been well characterized compared with secondary myelodysplastic syndrome or secondary acute myeloid leukemia. We present a report of two patients who developed ALL following complete remission of diffuse large B-cell lymphoma (DLBCL). The first case is more consistent with a therapy- related ALL as a PCR analysis of bone marrow aspirate revealed a distinct clone and the mixed-lineage leukemia gene rearrangement, commonly associated with exposure to topoisomerase II inhibitors. The second case is more consistent with clonal evolution given positive MYC and BCL2 fusion signals in the original diagnosis of DLBCL and the secondary ALL. PAGEPress Publications, Pavia, Italy 2019-06-14 /pmc/articles/PMC6589539/ /pubmed/31285810 http://dx.doi.org/10.4081/hr.2019.8100 Text en ©Copyright D. Gaut et al., 2019 http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Gaut, Daria
Bejjani, Anthony
Sasine, Joshua
Schiller, Gary
B-cell acute lymphoblastic leukemia as a secondary malignancy following diffuse large B-cell lymphoma
title B-cell acute lymphoblastic leukemia as a secondary malignancy following diffuse large B-cell lymphoma
title_full B-cell acute lymphoblastic leukemia as a secondary malignancy following diffuse large B-cell lymphoma
title_fullStr B-cell acute lymphoblastic leukemia as a secondary malignancy following diffuse large B-cell lymphoma
title_full_unstemmed B-cell acute lymphoblastic leukemia as a secondary malignancy following diffuse large B-cell lymphoma
title_short B-cell acute lymphoblastic leukemia as a secondary malignancy following diffuse large B-cell lymphoma
title_sort b-cell acute lymphoblastic leukemia as a secondary malignancy following diffuse large b-cell lymphoma
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6589539/
https://www.ncbi.nlm.nih.gov/pubmed/31285810
http://dx.doi.org/10.4081/hr.2019.8100
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