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Acute promyelocytic leukaemia (APML)


Is a subtype of AML (M3 subtype)


Clinical features:

  • Has a specific association with disseminated intravascular coagulation (DIC)
  • Patients may present with severe bleeding which worsens when treatment is started as the leukaemic blast cells break down, leading to further consumption of clotting factors and platelets

Treatment:

  • Regular, twice daily platelet transfusion and maintenance of the fibrinogen level with FFP as the chemotherapy is given
  • Provided that remission can be achieved, patients with APML have a better overall prognosis than patients with other subtypes of AML
  • Oral ATRA (all-trans-retinoic acid) can lead to achievement of CR in most patients with APML
  • Unfortunately, these remissions are not durable and, therefore, they must be consolidated with conventional chemotherapy


 


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