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A rare case of near-haploid acute lymphoblastic leukemia

Near-haploid acute lymphoblastic leukemia is seen in <1% of cases and carries an unfavorable prognosis. We report a case in an 18-year old male. He presented with two abnormal clones, one with 27–28 and one with 54–56 chromosomes. Near-haploidy (27–28) carries a poor prognosis and hyperdiploidy (...

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Autores principales: Gonzalez-Marques, William, Zaslav, Ann-Leslie, Balakrishnan, Dhana, Hogan, Laura, Ma, Yupo, Tully, Daniel, Fernicola, Paula, Ponce, Roxana, Lee, Htien, Mercado, Theresa, Ahmed, Tahmeena
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6488524/
https://www.ncbi.nlm.nih.gov/pubmed/31061791
http://dx.doi.org/10.1016/j.lrr.2019.04.006
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author Gonzalez-Marques, William
Zaslav, Ann-Leslie
Balakrishnan, Dhana
Hogan, Laura
Ma, Yupo
Tully, Daniel
Fernicola, Paula
Ponce, Roxana
Lee, Htien
Mercado, Theresa
Ahmed, Tahmeena
author_facet Gonzalez-Marques, William
Zaslav, Ann-Leslie
Balakrishnan, Dhana
Hogan, Laura
Ma, Yupo
Tully, Daniel
Fernicola, Paula
Ponce, Roxana
Lee, Htien
Mercado, Theresa
Ahmed, Tahmeena
author_sort Gonzalez-Marques, William
collection PubMed
description Near-haploid acute lymphoblastic leukemia is seen in <1% of cases and carries an unfavorable prognosis. We report a case in an 18-year old male. He presented with two abnormal clones, one with 27–28 and one with 54–56 chromosomes. Near-haploidy (27–28) carries a poor prognosis and hyperdiploidy (>50) has a good prognosis. The correct diagnosis was critical for this patient's prognosis and treatment. The patient achieved remission after a bone marrow transplant from a 10/10 HLA matched sibling donor. He relapsed six months later and expired seven months later. This case illustrates the need for careful standard and molecular cytogenetic analysis for accurate diagnosis and treatment for this rare type of ALL.
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spelling pubmed-64885242019-05-06 A rare case of near-haploid acute lymphoblastic leukemia Gonzalez-Marques, William Zaslav, Ann-Leslie Balakrishnan, Dhana Hogan, Laura Ma, Yupo Tully, Daniel Fernicola, Paula Ponce, Roxana Lee, Htien Mercado, Theresa Ahmed, Tahmeena Leuk Res Rep Article Near-haploid acute lymphoblastic leukemia is seen in <1% of cases and carries an unfavorable prognosis. We report a case in an 18-year old male. He presented with two abnormal clones, one with 27–28 and one with 54–56 chromosomes. Near-haploidy (27–28) carries a poor prognosis and hyperdiploidy (>50) has a good prognosis. The correct diagnosis was critical for this patient's prognosis and treatment. The patient achieved remission after a bone marrow transplant from a 10/10 HLA matched sibling donor. He relapsed six months later and expired seven months later. This case illustrates the need for careful standard and molecular cytogenetic analysis for accurate diagnosis and treatment for this rare type of ALL. Elsevier 2019-04-22 /pmc/articles/PMC6488524/ /pubmed/31061791 http://dx.doi.org/10.1016/j.lrr.2019.04.006 Text en Published by Elsevier Ltd. http://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
Gonzalez-Marques, William
Zaslav, Ann-Leslie
Balakrishnan, Dhana
Hogan, Laura
Ma, Yupo
Tully, Daniel
Fernicola, Paula
Ponce, Roxana
Lee, Htien
Mercado, Theresa
Ahmed, Tahmeena
A rare case of near-haploid acute lymphoblastic leukemia
title A rare case of near-haploid acute lymphoblastic leukemia
title_full A rare case of near-haploid acute lymphoblastic leukemia
title_fullStr A rare case of near-haploid acute lymphoblastic leukemia
title_full_unstemmed A rare case of near-haploid acute lymphoblastic leukemia
title_short A rare case of near-haploid acute lymphoblastic leukemia
title_sort rare case of near-haploid acute lymphoblastic leukemia
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6488524/
https://www.ncbi.nlm.nih.gov/pubmed/31061791
http://dx.doi.org/10.1016/j.lrr.2019.04.006
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