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Clinical, Hematological, and Cytogenetic Profile of Myelodysplastic Syndromes in Adults: A Three-year Cross-sectional Study

OBJECTIVES: Myelodysplastic syndromes (MDS) are a group of clonal hematological disorders with a diverse clinico-hematological profile. Studies in India have shown a different biology from the West. This study aimed to assess the clinicopathologic profile of MDS patients, classify them according to...

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Autores principales: Abraham, Latha, Paul, Mobin, D’Souza, Chryselle Olive, Sophy, M.P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: OMJ 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10152119/
https://www.ncbi.nlm.nih.gov/pubmed/37143488
http://dx.doi.org/10.5001/omj.2023.55
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author Abraham, Latha
Paul, Mobin
D’Souza, Chryselle Olive
Sophy, M.P.
author_facet Abraham, Latha
Paul, Mobin
D’Souza, Chryselle Olive
Sophy, M.P.
author_sort Abraham, Latha
collection PubMed
description OBJECTIVES: Myelodysplastic syndromes (MDS) are a group of clonal hematological disorders with a diverse clinico-hematological profile. Studies in India have shown a different biology from the West. This study aimed to assess the clinicopathologic profile of MDS patients, classify them according to the World Health Organization classification system, categorize them into International Prognostic Scoring System (IPSS) and the revised IPSS prognostic subgroups, and evaluate the treatment outcome. METHODS: A cross-sectional study was conducted on 48 patients diagnosed with MDS from January 2017 to December 2019 from Rajagiri Hospital, India. Clinical, hematological, and cytogenetic features were analyzed. The patients were stratified according to the IPSS and revised IPSS and were followed-up for a minimum of six months. RESULTS: The patients most affected were those in the seventh decade of life. We found a slight female preponderance and a mean age of 57.5 years in females and 67.7 years in males. Anemia was the most common manifestation of MDS. On the other hand, thrombocytopenia was found to be the least common cytopenia. MDS with multilineage dysplasia was the most common subtype. Cytogenetic abnormalities were seen in 29.5% of cases. Most of the patients were in the low-risk prognostic categories. CONCLUSIONS: Our patients were older when compared to those of other Indian studies, with most in the low-risk categories which were like Western data.
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spelling pubmed-101521192023-05-03 Clinical, Hematological, and Cytogenetic Profile of Myelodysplastic Syndromes in Adults: A Three-year Cross-sectional Study Abraham, Latha Paul, Mobin D’Souza, Chryselle Olive Sophy, M.P. Oman Med J Original Articles OBJECTIVES: Myelodysplastic syndromes (MDS) are a group of clonal hematological disorders with a diverse clinico-hematological profile. Studies in India have shown a different biology from the West. This study aimed to assess the clinicopathologic profile of MDS patients, classify them according to the World Health Organization classification system, categorize them into International Prognostic Scoring System (IPSS) and the revised IPSS prognostic subgroups, and evaluate the treatment outcome. METHODS: A cross-sectional study was conducted on 48 patients diagnosed with MDS from January 2017 to December 2019 from Rajagiri Hospital, India. Clinical, hematological, and cytogenetic features were analyzed. The patients were stratified according to the IPSS and revised IPSS and were followed-up for a minimum of six months. RESULTS: The patients most affected were those in the seventh decade of life. We found a slight female preponderance and a mean age of 57.5 years in females and 67.7 years in males. Anemia was the most common manifestation of MDS. On the other hand, thrombocytopenia was found to be the least common cytopenia. MDS with multilineage dysplasia was the most common subtype. Cytogenetic abnormalities were seen in 29.5% of cases. Most of the patients were in the low-risk prognostic categories. CONCLUSIONS: Our patients were older when compared to those of other Indian studies, with most in the low-risk categories which were like Western data. OMJ 2023-03-31 /pmc/articles/PMC10152119/ /pubmed/37143488 http://dx.doi.org/10.5001/omj.2023.55 Text en The OMJ is Published Bimonthly and Copyrighted 2023 by the OMSB. https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial (CC BY-NC) 4.0 License. http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/)
spellingShingle Original Articles
Abraham, Latha
Paul, Mobin
D’Souza, Chryselle Olive
Sophy, M.P.
Clinical, Hematological, and Cytogenetic Profile of Myelodysplastic Syndromes in Adults: A Three-year Cross-sectional Study
title Clinical, Hematological, and Cytogenetic Profile of Myelodysplastic Syndromes in Adults: A Three-year Cross-sectional Study
title_full Clinical, Hematological, and Cytogenetic Profile of Myelodysplastic Syndromes in Adults: A Three-year Cross-sectional Study
title_fullStr Clinical, Hematological, and Cytogenetic Profile of Myelodysplastic Syndromes in Adults: A Three-year Cross-sectional Study
title_full_unstemmed Clinical, Hematological, and Cytogenetic Profile of Myelodysplastic Syndromes in Adults: A Three-year Cross-sectional Study
title_short Clinical, Hematological, and Cytogenetic Profile of Myelodysplastic Syndromes in Adults: A Three-year Cross-sectional Study
title_sort clinical, hematological, and cytogenetic profile of myelodysplastic syndromes in adults: a three-year cross-sectional study
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10152119/
https://www.ncbi.nlm.nih.gov/pubmed/37143488
http://dx.doi.org/10.5001/omj.2023.55
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