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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-...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Carol Davila University Press
2013
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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 |
format | Online Article Text |
id | pubmed-3624642 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Carol Davila University Press |
record_format | MEDLINE/PubMed |
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
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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
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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
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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
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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
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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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