Authors :
Es-Sahli Khadija; Ameur Othmane; Amri Amine; Ilham Orchi; Zahid Hafid
Volume/Issue :
Volume 10 - 2025, Issue 10 - October
Google Scholar :
https://tinyurl.com/vpws5w7r
Scribd :
https://tinyurl.com/ywx7d5mt
DOI :
https://doi.org/10.38124/ijisrt/25oct602
Note : A published paper may take 4-5 working days from the publication date to appear in PlumX Metrics, Semantic Scholar, and ResearchGate.
Note : Google Scholar may take 30 to 40 days to display the article.
Abstract :
Background:
Acute leukemias are characterized by malignant proliferation of hematopoietic precursor cells (blasts), arrested at
specific differentiation stages and present in bone marrow, peripheral blood, and sometimes other tissues. Advances in
diagnostic techniques over the past decades have enabled better distinction between myeloid and lymphoid acute leukemias.
Objective:
To describe the epidemiological and cytological features of acute myeloid leukemias (AML) diagnosed at the
Hematology Laboratory of Mohammed V Military Hospital in Rabat over a 5-year period (2017–2022).
Methods:
We conducted a retrospective study of patients diagnosed with AML between January 1, 2017 and May 30, 2022.
Patients with incomplete records were excluded. Epidemiological, clinical, and laboratory data (complete blood counts, bone
marrow cytology, cytochemical staining) were collected from laboratory information systems. The diagnosis of AML was
based on ≥ 20% blasts in bone marrow (WHO 2008 criteria). Cytochemical myeloperoxidase (MPO) testing was performed
when myeloid morphology was unclear.
Results:
A total of 126 AML cases were included. The sex ratio (male/female) was 1.86. Two incidence peaks were observed: 10–
20 years and 40–70 years. The most frequent cytological subtypes were AML-M2 (22 %) and AML-M4 (17 %). Among
MPO+ AML cases: 70 % were unclassified MPO+, 9 % showed Auer bodies, 6 % had AML-M4 features, etc. Hemogram
anomalies included: anemia in 91 %, thrombocytopenia in 73 %, neutropenia in 37 %, hyperleukocytosis in 14 %,
pancytopenia in 27 %.
Conclusion:
AML in this Moroccan cohort display a bimodal age distribution and diverse cytological patterns dominated by MPO+
uncharacterized forms. The high prevalence of cytopenias underlines the severity of disease presentation. Further national
registries and molecular studies are warranted to enhance diagnostic and therapeutic capacity.
Keywords :
Acute Myeloid Leukemia; Epidemiology; Cytology; Morocco; Hematology; MPO.
References :
- Plesa C, Chelghoum Y, Plesa A, Elhamri M, Tigaud I, Michallet M, et al. Prognostic value of immunophenotyping in elderly patients with acute myeloid leukemia: A single-institution experience. Cancer. 2008 Feb 1;112(3):572–80.
- Imbert M, Wagner-Ballon O. Place du biologiste dans la prise en charge des leucémies aiguës: de l’hémogramme à la classification OMS. Rev Francoph des Lab. 2015(471):83–90.
- Jmili NB, Aziz ABA, Nagara M, Mahjoub T, Ghannem H, Mondher K. Profil épidémiologique et cytologique des leucémies aiguës: À propos de 193 cas colligés au centre Tunisien. Rev Française des Lab. 2005(369):23–8.
- Traoré C, Nebié K, Sawadogo S, Sanou AF, Héma A, Kafando É. Facteurs pronostiques et survie des leucémies aiguës de l’adulte au Burkina Faso. Médecine Trop Santé Int. 2023;3(3).
- Elloumi M, Aissaoui L, Laatiri MA. Évaluation nationale des traitements des leucémies aiguës myéloïdes de l’enfant (M3 exclues). 2004.
- Leucémies aiguës myéloïdes de l’adulte. EM Consulte.
- SFCE-P38 – Quand évoquer une leucémie devant des arthralgies avec hémogramme normal? EM Consulte.
- Castaigne S. Recommandations pour le diagnostic et le traitement des leucémies aiguës myéloblastiques. Hématologie. 2004;10(1):80–96.
Background:
Acute leukemias are characterized by malignant proliferation of hematopoietic precursor cells (blasts), arrested at
specific differentiation stages and present in bone marrow, peripheral blood, and sometimes other tissues. Advances in
diagnostic techniques over the past decades have enabled better distinction between myeloid and lymphoid acute leukemias.
Objective:
To describe the epidemiological and cytological features of acute myeloid leukemias (AML) diagnosed at the
Hematology Laboratory of Mohammed V Military Hospital in Rabat over a 5-year period (2017–2022).
Methods:
We conducted a retrospective study of patients diagnosed with AML between January 1, 2017 and May 30, 2022.
Patients with incomplete records were excluded. Epidemiological, clinical, and laboratory data (complete blood counts, bone
marrow cytology, cytochemical staining) were collected from laboratory information systems. The diagnosis of AML was
based on ≥ 20% blasts in bone marrow (WHO 2008 criteria). Cytochemical myeloperoxidase (MPO) testing was performed
when myeloid morphology was unclear.
Results:
A total of 126 AML cases were included. The sex ratio (male/female) was 1.86. Two incidence peaks were observed: 10–
20 years and 40–70 years. The most frequent cytological subtypes were AML-M2 (22 %) and AML-M4 (17 %). Among
MPO+ AML cases: 70 % were unclassified MPO+, 9 % showed Auer bodies, 6 % had AML-M4 features, etc. Hemogram
anomalies included: anemia in 91 %, thrombocytopenia in 73 %, neutropenia in 37 %, hyperleukocytosis in 14 %,
pancytopenia in 27 %.
Conclusion:
AML in this Moroccan cohort display a bimodal age distribution and diverse cytological patterns dominated by MPO+
uncharacterized forms. The high prevalence of cytopenias underlines the severity of disease presentation. Further national
registries and molecular studies are warranted to enhance diagnostic and therapeutic capacity.
Keywords :
Acute Myeloid Leukemia; Epidemiology; Cytology; Morocco; Hematology; MPO.