Acute leukaemia Flashcards
Natural history of Acute leukaemia
Result of accumulation of early myeloid and lymphoid precursors in the bone marrow, blood and other tissues.
Occurs by somatic mutation in a single cell within a population of early proginator cells
May arise de-novo in the terminal event of a pre-existing blood disorder / following chemo
Acute Myeloid Leukemia–> myeloid lineage e.g neutrophils, eosinophils
Acute lymphoblastic leukemia –> B & T cells etc
Presenting clinical features of AL
features of bone marrow failure: anaemia, infections, easy bruising and haemorrhage.
Organ infiltration by leukaemia cells may occur e.g. spleen, liver, meninges, testes and skin
common infection eg staph aureus infection of the orbit in a patient with AML. can get gum hypertrophy and bleeding in groin area.
Haematological features of AL
AML–> cells are monomorphic
ALL–> mainly nucleus
not developed cells. lack of diversity
Diagnosis
Immunological markers–> monoclonal antibody determination of surface antigen expression
Cytogenetics –> certain abnormalities correlate with prognosis eg translocaiton t(8;21) and t(15: 17) in AML = good prognosis.
monosomy 7 in AML and t(9;22) = bad prognosis
risk factors
- male
- old age (children recover very well)
- poor response to treatment due to genetics
- higher white cell count
management AML
induction treatment to obtain remission, the consolidaiton of further courses of combination chemo.
in younger patients consider bone marrow transplant (sibling best)
management ALL
All patients receive induction chemo, then consolidation chemo then prophylaxis of meningeal leukaemia with intrathecal methotrexate and cranial irradiation. bone marrow in bad risk patients required but risky procedure.
recognize neutropenic sepsis
- first all patients recieveing intensive chemo will become neutropenic for 10-21 days so will need hygienic isolation.
frequently the neutrophil count will fall to levels below 0.2 so can develop severe infections –> gram +/-ve
FEVER (PYREXIA)
treat neutropenic sepsis
try prevent with protective isolation, prophylatic antibiotics and use of granulocycte colony stimulating factors
TREAT: patietnt education and strict protocols for antimicrobial therapy.