Authors :
A Amri; K Essahli; A Hinda; D Talhik; H Zahid
Volume/Issue :
Volume 10 - 2025, Issue 3 - March
Google Scholar :
https://tinyurl.com/5xc99yz2
Scribd :
https://tinyurl.com/bdepb2yk
DOI :
https://doi.org/10.38124/ijisrt/25mar564
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Abstract :
Introduction
Myeloproliferative syndromes, including conditions such as chronic myelogenous leukemia, essential
thrombocythemia, polycythemia vera, and primary myelofibrosis, are characterized by the excessive production of stem
cells in the bone marrow. This study aims to describe the epidemiological and cytological profile of these syndromes at the
Mohammed V Military Instruction Hospital in Rabat. Materials and Methods: The study, conducted over one year, was
observational, cross-sectional, descriptive, and analytical. Data were collected from the hematology laboratory registers,
and statistical analysis was performed using IBM SPSS Statistics 19 and Microsoft Excel 2019.
Results
Fourteen suspected cases of myeloproliferative syndrome were identified, with a male predominance (69.2%) and an
average age of 57.75 years for CML, 61.75 years for PMF, 73 years for PV, and 81 years for ET. The main presentations
included leukocytosis for CML, thrombocytosis for PV, and multilineage dysplasia for PMF.
Conclusion
Our study at HMIMV Rabat highlights the importance of a multidisciplinary approach to myeloproliferative
syndromes. Advanced hematological and cytological analysis methods were crucial for confirming the diagnosis and
guiding treatment.
Keywords :
Myeloproliferative Syndromes, Hematopathy, Diagnosis.
References :
- Arber DA, Orazi A, Hasserjian R, et al , Le Beau MM, Bloomfield, Vardiman JW. The 2016 revision to the World HealthOrganization classification of myeloidneoplasms and acute leukemia. Blood. 2016;127(20):2391–2405
- Fowlkes, S., Murray, C., Fulford, A., et al. (2018). Néoplasies myéloprolifératives–Partie 1: survol du diagnostic et du traitement des NMP «classiques». Canadian OnCOlOgy nursing JOurnal, 28(4), 269.
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- Chakour M, Boumhil L, Maleb A, et al. LES SYNDROMES MYÉLOPROLIFÉRATIFS. Maroc Méd [Internet]. 2010 [cité 4 juill 2024] ;32(2).
- Leguay T, Mahon FX. Leucémie myéloïde chronique. Hématologie 2005, 2 : 187–205.
Introduction
Myeloproliferative syndromes, including conditions such as chronic myelogenous leukemia, essential
thrombocythemia, polycythemia vera, and primary myelofibrosis, are characterized by the excessive production of stem
cells in the bone marrow. This study aims to describe the epidemiological and cytological profile of these syndromes at the
Mohammed V Military Instruction Hospital in Rabat. Materials and Methods: The study, conducted over one year, was
observational, cross-sectional, descriptive, and analytical. Data were collected from the hematology laboratory registers,
and statistical analysis was performed using IBM SPSS Statistics 19 and Microsoft Excel 2019.
Results
Fourteen suspected cases of myeloproliferative syndrome were identified, with a male predominance (69.2%) and an
average age of 57.75 years for CML, 61.75 years for PMF, 73 years for PV, and 81 years for ET. The main presentations
included leukocytosis for CML, thrombocytosis for PV, and multilineage dysplasia for PMF.
Conclusion
Our study at HMIMV Rabat highlights the importance of a multidisciplinary approach to myeloproliferative
syndromes. Advanced hematological and cytological analysis methods were crucial for confirming the diagnosis and
guiding treatment.
Keywords :
Myeloproliferative Syndromes, Hematopathy, Diagnosis.