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Clinical features of leukaemic cell accumulation

Authoring team

These include:

  • bone and joint pain:
    • particularly in children with ALL

  • hyperleukocytosis:
    • due to high counts ( >100 x 10^9 / l) of circulating blasts
    • symptoms include headache, convulsion, fits, focal neurology and coma

  • tissue deposits of leukaemic cells:
    • for example, causing gum hypertrophy, stomatitis
    • more common in the myelomonocytic and monocytic varieties of AML

  • CNS involvement:
    • especially in ALL
    • occurs in 25 to 50% children and 10 to 20% of adults with acute leukaemia

  • acute haemostatic failure:
    • associated with the promyelocytic (M3) variant of AML in which the cells release cytoplasmic granular content, thus activating coagulation and fibrinolytic systems

  • lymphadenopathy and hepatosplenomegaly:
    • more common in ALL than in AML

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The content herein is provided for informational purposes and does not replace the need to apply professional clinical judgement when diagnosing or treating any medical condition. A licensed medical practitioner should be consulted for diagnosis and treatment of any and all medical conditions.

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