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The concomitant occurrence of JAK2V617F mutation and BCR/ABL transcript with phenotypic expression – an overlapping myeloproliferative disorder or two distinct diseases? - case report

The concomitant occurrence of JAK2617F mutation and BCR/ABL translocation is a rare event. It is unclear if this is a result of the clonal evolution or a separately emergence of two clones and if it could lead to the progression to a more aggressive phase of the disease. We present the case of a 61-...

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Autores principales: Ursuleac, I, Colita, AC, Adam, T, Jardan, C, Ilea, A, Coriu, D
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Carol Davila University Press 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3624642/
https://www.ncbi.nlm.nih.gov/pubmed/23599815
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author Ursuleac, I
Colita, AC
Adam, T
Jardan, C
Ilea, A
Coriu, D
author_facet Ursuleac, I
Colita, AC
Adam, T
Jardan, C
Ilea, A
Coriu, D
author_sort Ursuleac, I
collection PubMed
description The concomitant occurrence of JAK2617F mutation and BCR/ABL translocation is a rare event. It is unclear if this is a result of the clonal evolution or a separately emergence of two clones and if it could lead to the progression to a more aggressive phase of the disease. We present the case of a 61-year-old man diagnosed and treated for polycythaemia vera for 7 years, which evolved into chronic myeloid leukemia BCR/ABL positive and with JAK2617F mutated clone, that became dominant after an effective treatment with Imatinib. Abbreviations:WHO - World Health Organisation; CML - chronic myeloid leukemia; MPN - myeloproliferative neoplasms; PCR- polymerized chain reaction; TKI – tyrosine kinase inhibitors; PV - polycythemia vera; ET- essential thrombocythemia; PMF - primary myelofibrosis; ESR - erythrocyte sedimentation rate; WBC - white blood cell count; LDH - lacticodehydrogenase; ALP - alkaline leucocyte phosphatise
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spelling pubmed-36246422013-05-15 The concomitant occurrence of JAK2V617F mutation and BCR/ABL transcript with phenotypic expression – an overlapping myeloproliferative disorder or two distinct diseases? - case report Ursuleac, I Colita, AC Adam, T Jardan, C Ilea, A Coriu, D J Med Life Original Article The concomitant occurrence of JAK2617F mutation and BCR/ABL translocation is a rare event. It is unclear if this is a result of the clonal evolution or a separately emergence of two clones and if it could lead to the progression to a more aggressive phase of the disease. We present the case of a 61-year-old man diagnosed and treated for polycythaemia vera for 7 years, which evolved into chronic myeloid leukemia BCR/ABL positive and with JAK2617F mutated clone, that became dominant after an effective treatment with Imatinib. Abbreviations:WHO - World Health Organisation; CML - chronic myeloid leukemia; MPN - myeloproliferative neoplasms; PCR- polymerized chain reaction; TKI – tyrosine kinase inhibitors; PV - polycythemia vera; ET- essential thrombocythemia; PMF - primary myelofibrosis; ESR - erythrocyte sedimentation rate; WBC - white blood cell count; LDH - lacticodehydrogenase; ALP - alkaline leucocyte phosphatise Carol Davila University Press 2013-03-15 2013-03-25 /pmc/articles/PMC3624642/ /pubmed/23599815 Text en ©Carol Davila University Press http://creativecommons.org/licenses/by/2.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Ursuleac, I
Colita, AC
Adam, T
Jardan, C
Ilea, A
Coriu, D
The concomitant occurrence of JAK2V617F mutation and BCR/ABL transcript with phenotypic expression – an overlapping myeloproliferative disorder or two distinct diseases? - case report
title The concomitant occurrence of JAK2V617F mutation and BCR/ABL transcript with phenotypic expression – an overlapping myeloproliferative disorder or two distinct diseases? - case report
title_full The concomitant occurrence of JAK2V617F mutation and BCR/ABL transcript with phenotypic expression – an overlapping myeloproliferative disorder or two distinct diseases? - case report
title_fullStr The concomitant occurrence of JAK2V617F mutation and BCR/ABL transcript with phenotypic expression – an overlapping myeloproliferative disorder or two distinct diseases? - case report
title_full_unstemmed The concomitant occurrence of JAK2V617F mutation and BCR/ABL transcript with phenotypic expression – an overlapping myeloproliferative disorder or two distinct diseases? - case report
title_short The concomitant occurrence of JAK2V617F mutation and BCR/ABL transcript with phenotypic expression – an overlapping myeloproliferative disorder or two distinct diseases? - case report
title_sort concomitant occurrence of jak2v617f mutation and bcr/abl transcript with phenotypic expression – an overlapping myeloproliferative disorder or two distinct diseases? - case report
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3624642/
https://www.ncbi.nlm.nih.gov/pubmed/23599815
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