Incidence, patterns of clinical presentation, and haematological characteristics of paediatric acute myeloid leukaemia in Uganda: a retrospective analysis

dc.contributor.authorNyeko, Richard
dc.contributor.authorKruger, Mariana
dc.contributor.authorNiyonzima, Nixon
dc.contributor.authorAtwiine, Barnabas
dc.contributor.authorZungu, Jennifer
dc.contributor.authorKambugu, Joyce Balagadde
dc.contributor.authorVerhulst, Stijn
dc.contributor.authorHeerden, Jaques van
dc.date.accessioned2026-04-17T09:57:51Z
dc.date.issued2026
dc.description.abstractBackground Current understanding of paediatric acute myeloid leukaemia (AML) in Africa is limited. This study investigated the incidence, presentation pattern, and haematological profiles of paediatric AML in Uganda. Methods This retrospective cohort study examined the medical records of children under 18 years of age who were diagnosed with acute myeloid leukaemia (AML) at three cancer centres in Uganda from 2016 to 2022. Data included demographics, clinical features, and laboratory findings. Frequencies, bivariate analyses, and regression models were performed, with statistical significance set at p < 0.05. Results The study included 159 children diagnosed with AML, with a median age of 9.0 years (IQR 3.0–12.0). The incidence was 7.0/million children 0–17 years. The most common presenting symptoms were fever (84.3%), weight loss (44.0%), fatigue (40.9%), bleeding (35.8%), and bone pain (28.9%). Clinical findings at diagnosis included splenomegaly (40.9%), lymphadenopathy (39.6%), myeloid sarcoma (39.6%), and hepatomegaly (37.7%). The median (IQR) white blood cell (WBC) count at diagnosis was 32.0 × 10⁹/L (0.3–81.8). The predominant FAB subtype was M7 (n = 22, 24.4%), followed by M5 (n = 20, 22.2%). Acute promyelocytic leukaemia was seen in 13 (8.2%) patients, while 11 (6.9%) patients had myeloid leukaemia of Down syndrome. Cytogenetic analysis was limited to only 10 patients. There were significant differences in clinical characteristics by age with respect to splenomegaly, central nervous system involvement, and FAB subtype. Conclusions The incidence of paediatric AML in this study mirrors global patterns, with a higher-than-expected prevalence of the M7 subtype noted. In settings with limited resources, diagnosis relies mainly on clinical and morphological assessment. Broader access to cytogenetic and molecular testing could improve subtype identification and risk profiling.
dc.identifier.citationNyeko, R.,...[]et al.] (2026). Incidence, patterns of clinical presentation, and haematological characteristics of paediatric acute myeloid leukaemia in Uganda: a retrospective analysis
dc.identifier.urihttps://doi.org/10.1186/s12885-026-15580-8
dc.identifier.urihttps://ir.lirauni.ac.ug/handle/123456789/1115
dc.language.isoen
dc.publisherBMC
dc.subjectAcute myeloid leukaemia
dc.subjectPaediatric
dc.subjectIncidence
dc.subjectEpidemiology
dc.subjectUganda
dc.subjectAfrica
dc.titleIncidence, patterns of clinical presentation, and haematological characteristics of paediatric acute myeloid leukaemia in Uganda: a retrospective analysis
dc.typeArticle

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