This site is intended for healthcare professionals

Go to /sign-in page

You can view 5 more pages before signing in

Clinical features of leukaemic cell accumulation

Last reviewed dd mmm yyyy. Last edited dd mmm yyyy

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

Related pages

Create an account to add page annotations

Annotations allow you to add information to this page that would be handy to have on hand during a consultation. E.g. a website or number. This information will always show when you visit this page.