acute myeloid leukaemia

AML, APML...
Etiology median age 65
Epidemiology
Clinical presentation Signs of thrombocytopenia +/- extramedullary infiltration e.g. hepatosplenomegaly
Pathogenesis
Investigations: FBC: normochromic normocytic anaemia, thrombocytopenia, leukocytosis (5-20% of cases) AND neutropenia
Bone marrow: hypercellular, blast cells, Auer rods
Blood film: myeloid blasts, Auer rods

DIC may occur in APML
Management: prevention/management of Tumour lysis syndrome

APML = acute promyelocytic leukaemia