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Automated Detection of Dysplasia: Data Mining from Our Hematology Analyzers

Myelodysplastic syndromes (MDSs) are clonal hematopoietic diseases of the elderly, characterized by chronic cytopenia, ineffective and dysplastic hematopoiesis, recurrent genetic abnormalities and increased risk of progression to acute myeloid leukemia. Diagnosis on a complete blood count (CBC) can...

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Detalles Bibliográficos
Autores principales: Zhu, Jaja, Clauser, Sylvain, Freynet, Nicolas, Bardet, Valérie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9315627/
https://www.ncbi.nlm.nih.gov/pubmed/35885462
http://dx.doi.org/10.3390/diagnostics12071556
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author Zhu, Jaja
Clauser, Sylvain
Freynet, Nicolas
Bardet, Valérie
author_facet Zhu, Jaja
Clauser, Sylvain
Freynet, Nicolas
Bardet, Valérie
author_sort Zhu, Jaja
collection PubMed
description Myelodysplastic syndromes (MDSs) are clonal hematopoietic diseases of the elderly, characterized by chronic cytopenia, ineffective and dysplastic hematopoiesis, recurrent genetic abnormalities and increased risk of progression to acute myeloid leukemia. Diagnosis on a complete blood count (CBC) can be challenging due to numerous other non-neoplastic causes of cytopenias. New generations of hematology analyzers provide cell population data (CPD) that can be exploited to reliably detect MDSs from a routine CBC. In this review, we first describe the different technologies used to obtain CPD. We then give an overview of the currently available data regarding the performance of CPD for each lineage in the diagnostic workup of MDSs. Adequate exploitation of CPD can yield very strong diagnostic performances allowing for faster diagnosis and reduction of time-consuming slide reviews in the hematology laboratory.
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spelling pubmed-93156272022-07-27 Automated Detection of Dysplasia: Data Mining from Our Hematology Analyzers Zhu, Jaja Clauser, Sylvain Freynet, Nicolas Bardet, Valérie Diagnostics (Basel) Review Myelodysplastic syndromes (MDSs) are clonal hematopoietic diseases of the elderly, characterized by chronic cytopenia, ineffective and dysplastic hematopoiesis, recurrent genetic abnormalities and increased risk of progression to acute myeloid leukemia. Diagnosis on a complete blood count (CBC) can be challenging due to numerous other non-neoplastic causes of cytopenias. New generations of hematology analyzers provide cell population data (CPD) that can be exploited to reliably detect MDSs from a routine CBC. In this review, we first describe the different technologies used to obtain CPD. We then give an overview of the currently available data regarding the performance of CPD for each lineage in the diagnostic workup of MDSs. Adequate exploitation of CPD can yield very strong diagnostic performances allowing for faster diagnosis and reduction of time-consuming slide reviews in the hematology laboratory. MDPI 2022-06-26 /pmc/articles/PMC9315627/ /pubmed/35885462 http://dx.doi.org/10.3390/diagnostics12071556 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Zhu, Jaja
Clauser, Sylvain
Freynet, Nicolas
Bardet, Valérie
Automated Detection of Dysplasia: Data Mining from Our Hematology Analyzers
title Automated Detection of Dysplasia: Data Mining from Our Hematology Analyzers
title_full Automated Detection of Dysplasia: Data Mining from Our Hematology Analyzers
title_fullStr Automated Detection of Dysplasia: Data Mining from Our Hematology Analyzers
title_full_unstemmed Automated Detection of Dysplasia: Data Mining from Our Hematology Analyzers
title_short Automated Detection of Dysplasia: Data Mining from Our Hematology Analyzers
title_sort automated detection of dysplasia: data mining from our hematology analyzers
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9315627/
https://www.ncbi.nlm.nih.gov/pubmed/35885462
http://dx.doi.org/10.3390/diagnostics12071556
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