Cargando…

A case of acute myeloid leukemia (AML) with an unreported combination of chromosomal abnormalities: gain of isochromosome 5p, tetrasomy 8 and unbalanced translocation der(19)t(17;19)(q23;p13)

BACKGROUND: Acute myeloid leukemia (AML) comprises a spectrum of myeloid malignancies which are often associated with distinct chromosomal abnormalities, and the analysis of such abnormalities provides us with important information for disease classification, treatment selection and prognosis. Some...

Descripción completa

Detalles Bibliográficos
Autores principales: Paar, Christian, Herber, Gabriele, Voskova, Daniela, Fridrik, Michael, Stekel, Herbert, Berg, Jörg
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3852770/
https://www.ncbi.nlm.nih.gov/pubmed/24079663
http://dx.doi.org/10.1186/1755-8166-6-40
_version_ 1782478720959774720
author Paar, Christian
Herber, Gabriele
Voskova, Daniela
Fridrik, Michael
Stekel, Herbert
Berg, Jörg
author_facet Paar, Christian
Herber, Gabriele
Voskova, Daniela
Fridrik, Michael
Stekel, Herbert
Berg, Jörg
author_sort Paar, Christian
collection PubMed
description BACKGROUND: Acute myeloid leukemia (AML) comprises a spectrum of myeloid malignancies which are often associated with distinct chromosomal abnormalities, and the analysis of such abnormalities provides us with important information for disease classification, treatment selection and prognosis. Some chromosomal abnormalities albeit recurrent are rare such as tetrasomy 8 or isochromosome 5p. In addition, erratic chromosomal rearrangements may occur in AML, sometimes unbalanced and also accompanied by other abnormalities. Knowledge on the contribution of rare abnormalities to AML disease, progression and prognosis is limited. Here we report a unique case of acute monoblastic leukemia with gain of i(5)(p10), tetrasomy 8, an unbalanced translocation der(19)t(17;19)(q23;p13.3) and mutated NPM1. RESULTS: Bone marrow cells were examined by conventional karyotyping, fluorescence in situ hybridization (FISH) and mutation analysis at diagnosis and follow-up. At diagnosis we detected trisomy 8, an unbalanced translocation der(19)t(17;19)(q23;p13.3) and mutated NPM1. During the course of the disease we observed clonal evolution with gain of i(5)(p10), tetrasomy 8 and eventually duplication of der(19)t(17;19)(q23;p13.3). By using the der(19)t(17;19) as clonal marker, we found that i(5)(p10) and tetrasomy 8 were secondary genetic events and that tetrasomy 8 had clonally evolved from trisomy 8. CONCLUSIONS: This case of acute monoblastic leukemia presents a combination of rare chromosomal abnormalities including the unbalanced translocation der(19)t(17;19)(q23;p13.3), hitherto un-reported in AML. In addition, our case supports the hypothesis of a step-wise clonal evolution from trisomy 8 to tetrasomy 8 in AML. Reporting and collecting data of rare chromosomal abnormalities will add information to AML disease, progression and prognosis, and may eventually translate to improved patient management.
format Online
Article
Text
id pubmed-3852770
institution National Center for Biotechnology Information
language English
publishDate 2013
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-38527702013-12-06 A case of acute myeloid leukemia (AML) with an unreported combination of chromosomal abnormalities: gain of isochromosome 5p, tetrasomy 8 and unbalanced translocation der(19)t(17;19)(q23;p13) Paar, Christian Herber, Gabriele Voskova, Daniela Fridrik, Michael Stekel, Herbert Berg, Jörg Mol Cytogenet Case Report BACKGROUND: Acute myeloid leukemia (AML) comprises a spectrum of myeloid malignancies which are often associated with distinct chromosomal abnormalities, and the analysis of such abnormalities provides us with important information for disease classification, treatment selection and prognosis. Some chromosomal abnormalities albeit recurrent are rare such as tetrasomy 8 or isochromosome 5p. In addition, erratic chromosomal rearrangements may occur in AML, sometimes unbalanced and also accompanied by other abnormalities. Knowledge on the contribution of rare abnormalities to AML disease, progression and prognosis is limited. Here we report a unique case of acute monoblastic leukemia with gain of i(5)(p10), tetrasomy 8, an unbalanced translocation der(19)t(17;19)(q23;p13.3) and mutated NPM1. RESULTS: Bone marrow cells were examined by conventional karyotyping, fluorescence in situ hybridization (FISH) and mutation analysis at diagnosis and follow-up. At diagnosis we detected trisomy 8, an unbalanced translocation der(19)t(17;19)(q23;p13.3) and mutated NPM1. During the course of the disease we observed clonal evolution with gain of i(5)(p10), tetrasomy 8 and eventually duplication of der(19)t(17;19)(q23;p13.3). By using the der(19)t(17;19) as clonal marker, we found that i(5)(p10) and tetrasomy 8 were secondary genetic events and that tetrasomy 8 had clonally evolved from trisomy 8. CONCLUSIONS: This case of acute monoblastic leukemia presents a combination of rare chromosomal abnormalities including the unbalanced translocation der(19)t(17;19)(q23;p13.3), hitherto un-reported in AML. In addition, our case supports the hypothesis of a step-wise clonal evolution from trisomy 8 to tetrasomy 8 in AML. Reporting and collecting data of rare chromosomal abnormalities will add information to AML disease, progression and prognosis, and may eventually translate to improved patient management. BioMed Central 2013-09-30 /pmc/articles/PMC3852770/ /pubmed/24079663 http://dx.doi.org/10.1186/1755-8166-6-40 Text en Copyright © 2013 Paar et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Paar, Christian
Herber, Gabriele
Voskova, Daniela
Fridrik, Michael
Stekel, Herbert
Berg, Jörg
A case of acute myeloid leukemia (AML) with an unreported combination of chromosomal abnormalities: gain of isochromosome 5p, tetrasomy 8 and unbalanced translocation der(19)t(17;19)(q23;p13)
title A case of acute myeloid leukemia (AML) with an unreported combination of chromosomal abnormalities: gain of isochromosome 5p, tetrasomy 8 and unbalanced translocation der(19)t(17;19)(q23;p13)
title_full A case of acute myeloid leukemia (AML) with an unreported combination of chromosomal abnormalities: gain of isochromosome 5p, tetrasomy 8 and unbalanced translocation der(19)t(17;19)(q23;p13)
title_fullStr A case of acute myeloid leukemia (AML) with an unreported combination of chromosomal abnormalities: gain of isochromosome 5p, tetrasomy 8 and unbalanced translocation der(19)t(17;19)(q23;p13)
title_full_unstemmed A case of acute myeloid leukemia (AML) with an unreported combination of chromosomal abnormalities: gain of isochromosome 5p, tetrasomy 8 and unbalanced translocation der(19)t(17;19)(q23;p13)
title_short A case of acute myeloid leukemia (AML) with an unreported combination of chromosomal abnormalities: gain of isochromosome 5p, tetrasomy 8 and unbalanced translocation der(19)t(17;19)(q23;p13)
title_sort case of acute myeloid leukemia (aml) with an unreported combination of chromosomal abnormalities: gain of isochromosome 5p, tetrasomy 8 and unbalanced translocation der(19)t(17;19)(q23;p13)
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3852770/
https://www.ncbi.nlm.nih.gov/pubmed/24079663
http://dx.doi.org/10.1186/1755-8166-6-40
work_keys_str_mv AT paarchristian acaseofacutemyeloidleukemiaamlwithanunreportedcombinationofchromosomalabnormalitiesgainofisochromosome5ptetrasomy8andunbalancedtranslocationder19t1719q23p13
AT herbergabriele acaseofacutemyeloidleukemiaamlwithanunreportedcombinationofchromosomalabnormalitiesgainofisochromosome5ptetrasomy8andunbalancedtranslocationder19t1719q23p13
AT voskovadaniela acaseofacutemyeloidleukemiaamlwithanunreportedcombinationofchromosomalabnormalitiesgainofisochromosome5ptetrasomy8andunbalancedtranslocationder19t1719q23p13
AT fridrikmichael acaseofacutemyeloidleukemiaamlwithanunreportedcombinationofchromosomalabnormalitiesgainofisochromosome5ptetrasomy8andunbalancedtranslocationder19t1719q23p13
AT stekelherbert acaseofacutemyeloidleukemiaamlwithanunreportedcombinationofchromosomalabnormalitiesgainofisochromosome5ptetrasomy8andunbalancedtranslocationder19t1719q23p13
AT bergjorg acaseofacutemyeloidleukemiaamlwithanunreportedcombinationofchromosomalabnormalitiesgainofisochromosome5ptetrasomy8andunbalancedtranslocationder19t1719q23p13
AT paarchristian caseofacutemyeloidleukemiaamlwithanunreportedcombinationofchromosomalabnormalitiesgainofisochromosome5ptetrasomy8andunbalancedtranslocationder19t1719q23p13
AT herbergabriele caseofacutemyeloidleukemiaamlwithanunreportedcombinationofchromosomalabnormalitiesgainofisochromosome5ptetrasomy8andunbalancedtranslocationder19t1719q23p13
AT voskovadaniela caseofacutemyeloidleukemiaamlwithanunreportedcombinationofchromosomalabnormalitiesgainofisochromosome5ptetrasomy8andunbalancedtranslocationder19t1719q23p13
AT fridrikmichael caseofacutemyeloidleukemiaamlwithanunreportedcombinationofchromosomalabnormalitiesgainofisochromosome5ptetrasomy8andunbalancedtranslocationder19t1719q23p13
AT stekelherbert caseofacutemyeloidleukemiaamlwithanunreportedcombinationofchromosomalabnormalitiesgainofisochromosome5ptetrasomy8andunbalancedtranslocationder19t1719q23p13
AT bergjorg caseofacutemyeloidleukemiaamlwithanunreportedcombinationofchromosomalabnormalitiesgainofisochromosome5ptetrasomy8andunbalancedtranslocationder19t1719q23p13