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B/T mixed phenotype acute leukemia with high hyperdiploidy and lineage switch to B-cell acute leukemia
Acute leukemias are often of myeloid or lymphoid origin. However, some acute leukemias revealed an undefined differentiation into a single lineage. Mixed phenotype acute leukemia (MPAL) is an uncommon diagnosis were blasts can share B/T/myeloid phenotype. Here, we report a rare case of a 17-year-old...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8777379/ https://www.ncbi.nlm.nih.gov/pubmed/35079568 http://dx.doi.org/10.1016/j.lrr.2022.100289 |
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author | Skhoun, Hanaa Khattab, Mohammed Chebihi, Zahra Takki Belkhayat, Aziza Dakka, Nadia BaghdadI, Jamila EL |
author_facet | Skhoun, Hanaa Khattab, Mohammed Chebihi, Zahra Takki Belkhayat, Aziza Dakka, Nadia BaghdadI, Jamila EL |
author_sort | Skhoun, Hanaa |
collection | PubMed |
description | Acute leukemias are often of myeloid or lymphoid origin. However, some acute leukemias revealed an undefined differentiation into a single lineage. Mixed phenotype acute leukemia (MPAL) is an uncommon diagnosis were blasts can share B/T/myeloid phenotype. Here, we report a rare case of a 17-year-old Moroccan female diagnosed with B/T mixed phenotype acute leukemia and a high hyperdiploid karyotype who relapsed after one year of complete remission with a lineage switch to B-cell acute lymphoblastic leukemia. This case report corroborates the disclosed findings about the high occurence of abnormal karyotypes and poor prognosis of MPAL. |
format | Online Article Text |
id | pubmed-8777379 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-87773792022-01-24 B/T mixed phenotype acute leukemia with high hyperdiploidy and lineage switch to B-cell acute leukemia Skhoun, Hanaa Khattab, Mohammed Chebihi, Zahra Takki Belkhayat, Aziza Dakka, Nadia BaghdadI, Jamila EL Leuk Res Rep Article Acute leukemias are often of myeloid or lymphoid origin. However, some acute leukemias revealed an undefined differentiation into a single lineage. Mixed phenotype acute leukemia (MPAL) is an uncommon diagnosis were blasts can share B/T/myeloid phenotype. Here, we report a rare case of a 17-year-old Moroccan female diagnosed with B/T mixed phenotype acute leukemia and a high hyperdiploid karyotype who relapsed after one year of complete remission with a lineage switch to B-cell acute lymphoblastic leukemia. This case report corroborates the disclosed findings about the high occurence of abnormal karyotypes and poor prognosis of MPAL. Elsevier 2022-01-15 /pmc/articles/PMC8777379/ /pubmed/35079568 http://dx.doi.org/10.1016/j.lrr.2022.100289 Text en © 2022 Published by Elsevier Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Skhoun, Hanaa Khattab, Mohammed Chebihi, Zahra Takki Belkhayat, Aziza Dakka, Nadia BaghdadI, Jamila EL B/T mixed phenotype acute leukemia with high hyperdiploidy and lineage switch to B-cell acute leukemia |
title | B/T mixed phenotype acute leukemia with high hyperdiploidy and lineage switch to B-cell acute leukemia |
title_full | B/T mixed phenotype acute leukemia with high hyperdiploidy and lineage switch to B-cell acute leukemia |
title_fullStr | B/T mixed phenotype acute leukemia with high hyperdiploidy and lineage switch to B-cell acute leukemia |
title_full_unstemmed | B/T mixed phenotype acute leukemia with high hyperdiploidy and lineage switch to B-cell acute leukemia |
title_short | B/T mixed phenotype acute leukemia with high hyperdiploidy and lineage switch to B-cell acute leukemia |
title_sort | b/t mixed phenotype acute leukemia with high hyperdiploidy and lineage switch to b-cell acute leukemia |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8777379/ https://www.ncbi.nlm.nih.gov/pubmed/35079568 http://dx.doi.org/10.1016/j.lrr.2022.100289 |
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