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Colony-stimulating Factor 3 Receptor Mutated Chronic Neutrophilic Leukemia: A Rare Case Report

Chronic neutrophilic leukemia (CNL) is a rare myeloproliferative neoplasm, which is characterized by sustained peripheral leukocytosis with neutrophilia, hepatosplenomegaly, and hypercellularity of the bone marrow, with less than 5% myeloblasts along with normal neutrophil maturation and no dysplasi...

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Detalles Bibliográficos
Autores principales: Thapa, Bicky, Jamhour, Christopher, Chahine, Johnny, Rogers, Heesun J, Daw, Hamed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6248686/
https://www.ncbi.nlm.nih.gov/pubmed/30473959
http://dx.doi.org/10.7759/cureus.3326
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author Thapa, Bicky
Jamhour, Christopher
Chahine, Johnny
Rogers, Heesun J
Daw, Hamed
author_facet Thapa, Bicky
Jamhour, Christopher
Chahine, Johnny
Rogers, Heesun J
Daw, Hamed
author_sort Thapa, Bicky
collection PubMed
description Chronic neutrophilic leukemia (CNL) is a rare myeloproliferative neoplasm, which is characterized by sustained peripheral leukocytosis with neutrophilia, hepatosplenomegaly, and hypercellularity of the bone marrow, with less than 5% myeloblasts along with normal neutrophil maturation and no dysplasia. In 2016, World Health Organization (WHO) included activating mutations in the gene for colony-stimulating factor 3 receptor (CSF3R) as one of the diagnostic criteria with CSF3RT618I being the most common mutation. We report a rare case of CNL (JAK2V617F negative, BCR-ABL1 negative, CSF3RT618I positive) in an elderly female who had an aggressive clinical course of the disease.
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spelling pubmed-62486862018-11-23 Colony-stimulating Factor 3 Receptor Mutated Chronic Neutrophilic Leukemia: A Rare Case Report Thapa, Bicky Jamhour, Christopher Chahine, Johnny Rogers, Heesun J Daw, Hamed Cureus Oncology Chronic neutrophilic leukemia (CNL) is a rare myeloproliferative neoplasm, which is characterized by sustained peripheral leukocytosis with neutrophilia, hepatosplenomegaly, and hypercellularity of the bone marrow, with less than 5% myeloblasts along with normal neutrophil maturation and no dysplasia. In 2016, World Health Organization (WHO) included activating mutations in the gene for colony-stimulating factor 3 receptor (CSF3R) as one of the diagnostic criteria with CSF3RT618I being the most common mutation. We report a rare case of CNL (JAK2V617F negative, BCR-ABL1 negative, CSF3RT618I positive) in an elderly female who had an aggressive clinical course of the disease. Cureus 2018-09-18 /pmc/articles/PMC6248686/ /pubmed/30473959 http://dx.doi.org/10.7759/cureus.3326 Text en Copyright © 2018, Thapa et al. http://creativecommons.org/licenses/by/3.0/ 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 author and source are credited.
spellingShingle Oncology
Thapa, Bicky
Jamhour, Christopher
Chahine, Johnny
Rogers, Heesun J
Daw, Hamed
Colony-stimulating Factor 3 Receptor Mutated Chronic Neutrophilic Leukemia: A Rare Case Report
title Colony-stimulating Factor 3 Receptor Mutated Chronic Neutrophilic Leukemia: A Rare Case Report
title_full Colony-stimulating Factor 3 Receptor Mutated Chronic Neutrophilic Leukemia: A Rare Case Report
title_fullStr Colony-stimulating Factor 3 Receptor Mutated Chronic Neutrophilic Leukemia: A Rare Case Report
title_full_unstemmed Colony-stimulating Factor 3 Receptor Mutated Chronic Neutrophilic Leukemia: A Rare Case Report
title_short Colony-stimulating Factor 3 Receptor Mutated Chronic Neutrophilic Leukemia: A Rare Case Report
title_sort colony-stimulating factor 3 receptor mutated chronic neutrophilic leukemia: a rare case report
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6248686/
https://www.ncbi.nlm.nih.gov/pubmed/30473959
http://dx.doi.org/10.7759/cureus.3326
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