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Myelodysplastic syndrome: validation of flow cytometry multilineage score system

OBJECTIVE: To validate multilineage score system correlating results of flow cytometry, cytogenetics, cytomorphology and histology from samples of patients with suspected myelodysplastic syndrome or cytopenia of unknown origin. METHODS: A retrospective study analyzing laboratory data of 49 patients...

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Autores principales: de Araújo, Helena Varela, Correia, Rodolfo Patussi, Bento, Laiz Cameirão, Vaz, Andressa da Costa, de Sousa, Flávia Arandas, Alexandre, Anderson Marega, Schimidell, Daniela, Pedro, Eduardo de Carvalho, Ioshida, Márcia Regina, Barroso, Rodrigo de Souza, Bacal, Nydia Strachman
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Instituto Israelita de Ensino e Pesquisa Albert Einstein 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6986454/
https://www.ncbi.nlm.nih.gov/pubmed/31994605
http://dx.doi.org/10.31744/einstein_journal/2020AO4966
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author de Araújo, Helena Varela
Correia, Rodolfo Patussi
Bento, Laiz Cameirão
Vaz, Andressa da Costa
de Sousa, Flávia Arandas
Alexandre, Anderson Marega
Schimidell, Daniela
Pedro, Eduardo de Carvalho
Ioshida, Márcia Regina
Barroso, Rodrigo de Souza
Bacal, Nydia Strachman
author_facet de Araújo, Helena Varela
Correia, Rodolfo Patussi
Bento, Laiz Cameirão
Vaz, Andressa da Costa
de Sousa, Flávia Arandas
Alexandre, Anderson Marega
Schimidell, Daniela
Pedro, Eduardo de Carvalho
Ioshida, Márcia Regina
Barroso, Rodrigo de Souza
Bacal, Nydia Strachman
author_sort de Araújo, Helena Varela
collection PubMed
description OBJECTIVE: To validate multilineage score system correlating results of flow cytometry, cytogenetics, cytomorphology and histology from samples of patients with suspected myelodysplastic syndrome or cytopenia of unknown origin. METHODS: A retrospective study analyzing laboratory data of 49 patients with suspected myelodysplastic syndrome or cytopenia of unknown origin, carried out between May and September 2017. The inclusion criteria were availability of flow cytometry results, and at least one more method, such as morphology, histology or cytogenetics. Thirty-eight patients were classified as diagnosis of myelodysplastic syndromes, whereas 11 were classified as normal. Patients were evaluated based on score systems, Ogata score and flow cytometry multilineage score. RESULTS: Comparing the scores obtained in the Ogata score and the multilineage score, it was observed that in four cases the Ogata score was zero or 1 point, while the multilineage score was higher than 3 points. In addition, in 12 cases with Ogata score of 2, the multilineage score was greater than 3. CONCLUSION: The flow cytometry multilineage score system demonstrated to be more effective in dysplasia analysis, by assessing the erythroid, monocytic, granulocytic and precursor cell lineages, apart from the parameters evaluated by the Ogata score.
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spelling pubmed-69864542020-02-10 Myelodysplastic syndrome: validation of flow cytometry multilineage score system de Araújo, Helena Varela Correia, Rodolfo Patussi Bento, Laiz Cameirão Vaz, Andressa da Costa de Sousa, Flávia Arandas Alexandre, Anderson Marega Schimidell, Daniela Pedro, Eduardo de Carvalho Ioshida, Márcia Regina Barroso, Rodrigo de Souza Bacal, Nydia Strachman Einstein (Sao Paulo) Original Article OBJECTIVE: To validate multilineage score system correlating results of flow cytometry, cytogenetics, cytomorphology and histology from samples of patients with suspected myelodysplastic syndrome or cytopenia of unknown origin. METHODS: A retrospective study analyzing laboratory data of 49 patients with suspected myelodysplastic syndrome or cytopenia of unknown origin, carried out between May and September 2017. The inclusion criteria were availability of flow cytometry results, and at least one more method, such as morphology, histology or cytogenetics. Thirty-eight patients were classified as diagnosis of myelodysplastic syndromes, whereas 11 were classified as normal. Patients were evaluated based on score systems, Ogata score and flow cytometry multilineage score. RESULTS: Comparing the scores obtained in the Ogata score and the multilineage score, it was observed that in four cases the Ogata score was zero or 1 point, while the multilineage score was higher than 3 points. In addition, in 12 cases with Ogata score of 2, the multilineage score was greater than 3. CONCLUSION: The flow cytometry multilineage score system demonstrated to be more effective in dysplasia analysis, by assessing the erythroid, monocytic, granulocytic and precursor cell lineages, apart from the parameters evaluated by the Ogata score. Instituto Israelita de Ensino e Pesquisa Albert Einstein 2020-01-23 /pmc/articles/PMC6986454/ /pubmed/31994605 http://dx.doi.org/10.31744/einstein_journal/2020AO4966 Text en http://creativecommons.org/licenses/by/4.0/ 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
de Araújo, Helena Varela
Correia, Rodolfo Patussi
Bento, Laiz Cameirão
Vaz, Andressa da Costa
de Sousa, Flávia Arandas
Alexandre, Anderson Marega
Schimidell, Daniela
Pedro, Eduardo de Carvalho
Ioshida, Márcia Regina
Barroso, Rodrigo de Souza
Bacal, Nydia Strachman
Myelodysplastic syndrome: validation of flow cytometry multilineage score system
title Myelodysplastic syndrome: validation of flow cytometry multilineage score system
title_full Myelodysplastic syndrome: validation of flow cytometry multilineage score system
title_fullStr Myelodysplastic syndrome: validation of flow cytometry multilineage score system
title_full_unstemmed Myelodysplastic syndrome: validation of flow cytometry multilineage score system
title_short Myelodysplastic syndrome: validation of flow cytometry multilineage score system
title_sort myelodysplastic syndrome: validation of flow cytometry multilineage score system
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6986454/
https://www.ncbi.nlm.nih.gov/pubmed/31994605
http://dx.doi.org/10.31744/einstein_journal/2020AO4966
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