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Therapy related acute myeloid leukemia with t(10:16): a rare entity
Treatment related myelodysplastic syndrome (t-MDS) and acute myeloid leukemia (t-AML) are well known complications after chemotherapy for various hematologic and non-hematologic malignancies. Alkylating agents and Topoisomerase inhibitors are most widely studied in this regard. There is growing conc...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
PAGEPress Publications
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3269801/ https://www.ncbi.nlm.nih.gov/pubmed/22593815 http://dx.doi.org/10.4081/hr.2011.e23 |
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author | Uppal, Guldeep K. Leighton, John Da Costa, Deline Czulewicz, Andrew Palazzo, Irma E. |
author_facet | Uppal, Guldeep K. Leighton, John Da Costa, Deline Czulewicz, Andrew Palazzo, Irma E. |
author_sort | Uppal, Guldeep K. |
collection | PubMed |
description | Treatment related myelodysplastic syndrome (t-MDS) and acute myeloid leukemia (t-AML) are well known complications after chemotherapy for various hematologic and non-hematologic malignancies. Alkylating agents and Topoisomerase inhibitors are most widely studied in this regard. There is growing concern about occurrence of t-MDS, t-MDS/AML and t-AML in patients of CLL treated with nucleoside analogues especially in combination with alkylating agents. Exact incidence and pathogenesis of nucleoside analogue related MDS/AML is not clear at this time. We hereby report a case of t-AML in a patient treated with Fludarabine, Cyclophosphamide and Rituximab (FCR) for CLL. The cytogenetic studies revealed a unique translocation t (10:16), that has been reported in very few cases of therapy related AML and pediatric AML. |
format | Online Article Text |
id | pubmed-3269801 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | PAGEPress Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-32698012012-05-16 Therapy related acute myeloid leukemia with t(10:16): a rare entity Uppal, Guldeep K. Leighton, John Da Costa, Deline Czulewicz, Andrew Palazzo, Irma E. Hematol Rep Case Report Treatment related myelodysplastic syndrome (t-MDS) and acute myeloid leukemia (t-AML) are well known complications after chemotherapy for various hematologic and non-hematologic malignancies. Alkylating agents and Topoisomerase inhibitors are most widely studied in this regard. There is growing concern about occurrence of t-MDS, t-MDS/AML and t-AML in patients of CLL treated with nucleoside analogues especially in combination with alkylating agents. Exact incidence and pathogenesis of nucleoside analogue related MDS/AML is not clear at this time. We hereby report a case of t-AML in a patient treated with Fludarabine, Cyclophosphamide and Rituximab (FCR) for CLL. The cytogenetic studies revealed a unique translocation t (10:16), that has been reported in very few cases of therapy related AML and pediatric AML. PAGEPress Publications 2011-12-15 /pmc/articles/PMC3269801/ /pubmed/22593815 http://dx.doi.org/10.4081/hr.2011.e23 Text en ©Copyright G.K. Uppal et al., 2011 This work is licensed under a Creative Commons Attribution NonCommercial 3.0 License (CC BY-NC 3.0). Licensee PAGEPress, Italy |
spellingShingle | Case Report Uppal, Guldeep K. Leighton, John Da Costa, Deline Czulewicz, Andrew Palazzo, Irma E. Therapy related acute myeloid leukemia with t(10:16): a rare entity |
title | Therapy related acute myeloid leukemia with t(10:16): a rare entity |
title_full | Therapy related acute myeloid leukemia with t(10:16): a rare entity |
title_fullStr | Therapy related acute myeloid leukemia with t(10:16): a rare entity |
title_full_unstemmed | Therapy related acute myeloid leukemia with t(10:16): a rare entity |
title_short | Therapy related acute myeloid leukemia with t(10:16): a rare entity |
title_sort | therapy related acute myeloid leukemia with t(10:16): a rare entity |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3269801/ https://www.ncbi.nlm.nih.gov/pubmed/22593815 http://dx.doi.org/10.4081/hr.2011.e23 |
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