Abstract
Haematological involvement of systemic lupus erythematosus (SLE) – which ranges from the well-described haemolytic anaemia to macrophage activation syndrome – has a large impact on both morbidity and mortality. On the other hand, association between haematological malignities and SLE – in terms of pathophysiology and molecular genetics – is an obscure entity which has not been clarified evidently to date. Herein, we present a six-year-old female with the diagnosis of SLE who developed acute lymphoblastic leukaemia following a period of myelodysplasia. It could possibly be coincidental; however, persistent cytopenia, prominent dysplasia on bone marrow smears and azathioprine treatment may be considered as possible triggers for the development of leukaemia in the present case.
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