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Atypical chronic myeloid leukemia BCR-ABL 1 negative: A case report and literature review
Atypical chronic myeloid leukemia (aCML), BCR-ABL1 negative is a rare myelodysplastic syndrome/myeloproliferative neoplasm for which no current standard of care exists. The blood smear of patients with aCML showed prominent immature granulocytosis, and granulocytic dysplasia. We admitted a 58-year-o...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6551503/ https://www.ncbi.nlm.nih.gov/pubmed/31194134 http://dx.doi.org/10.1016/j.lrr.2019.100172 |
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author | Belkhair, Jihane Raissi, Abderahim Elyahyaoui, Hicham Ameur, Mustapha Ait Chakour, Mohamed |
author_facet | Belkhair, Jihane Raissi, Abderahim Elyahyaoui, Hicham Ameur, Mustapha Ait Chakour, Mohamed |
author_sort | Belkhair, Jihane |
collection | PubMed |
description | Atypical chronic myeloid leukemia (aCML), BCR-ABL1 negative is a rare myelodysplastic syndrome/myeloproliferative neoplasm for which no current standard of care exists. The blood smear of patients with aCML showed prominent immature granulocytosis, and granulocytic dysplasia. We admitted a 58-year-old man with splenomegaly, hyperleukocytosis, anemia, and thrombocytopenia; then cytology, cytogenetic and molecular biology analysis of bone morrow were performed and the diagnosis of aCML was made according to 2016 World Health Organization diagnostic criteria. The patient was initially treated by chemotherapy; the patient achieved an aggravation of anemia. This motivated the change of treatment. |
format | Online Article Text |
id | pubmed-6551503 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-65515032019-06-10 Atypical chronic myeloid leukemia BCR-ABL 1 negative: A case report and literature review Belkhair, Jihane Raissi, Abderahim Elyahyaoui, Hicham Ameur, Mustapha Ait Chakour, Mohamed Leuk Res Rep Article Atypical chronic myeloid leukemia (aCML), BCR-ABL1 negative is a rare myelodysplastic syndrome/myeloproliferative neoplasm for which no current standard of care exists. The blood smear of patients with aCML showed prominent immature granulocytosis, and granulocytic dysplasia. We admitted a 58-year-old man with splenomegaly, hyperleukocytosis, anemia, and thrombocytopenia; then cytology, cytogenetic and molecular biology analysis of bone morrow were performed and the diagnosis of aCML was made according to 2016 World Health Organization diagnostic criteria. The patient was initially treated by chemotherapy; the patient achieved an aggravation of anemia. This motivated the change of treatment. Elsevier 2019-05-25 /pmc/articles/PMC6551503/ /pubmed/31194134 http://dx.doi.org/10.1016/j.lrr.2019.100172 Text en © 2019 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 Belkhair, Jihane Raissi, Abderahim Elyahyaoui, Hicham Ameur, Mustapha Ait Chakour, Mohamed Atypical chronic myeloid leukemia BCR-ABL 1 negative: A case report and literature review |
title | Atypical chronic myeloid leukemia BCR-ABL 1 negative: A case report and literature review |
title_full | Atypical chronic myeloid leukemia BCR-ABL 1 negative: A case report and literature review |
title_fullStr | Atypical chronic myeloid leukemia BCR-ABL 1 negative: A case report and literature review |
title_full_unstemmed | Atypical chronic myeloid leukemia BCR-ABL 1 negative: A case report and literature review |
title_short | Atypical chronic myeloid leukemia BCR-ABL 1 negative: A case report and literature review |
title_sort | atypical chronic myeloid leukemia bcr-abl 1 negative: a case report and literature review |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6551503/ https://www.ncbi.nlm.nih.gov/pubmed/31194134 http://dx.doi.org/10.1016/j.lrr.2019.100172 |
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