Leukaemia Flashcards
what are the kinetics of normal haemopoiesis
Self renewal (stem cells) Proliferation Differentiation/lineage commitment Maturation Apoptosis
what is malignant haemopoiesis characterised by
increased numbers of often dysfunctional cells and may have loss of the normal haemopoietic reserve.
what is needed for malignant haemopoiesis
One or more of the following:
Increased proliferation
Lack of differentiation
Lack of maturation
Lack of apoptosis
what is acute leukaemia
abnormal proliferation and maturation
- bone marrow over run by mononuclear cells = loss of normal variation
- cells unable to mature
what are the types of mutations seen in blood cells
Driver mutation = a mutation that gives a selective advantage to a clone through either increasing its survival or reproduction. Cause clonal expansions.
Passenger mutation = mutations that have no consequence to the cell or growth advantage
what is the most common childhood cancer
acute lymphoblastic leukaemia
what is a key features of malignant haemopoiesis
monoclonal
what are the types go haematological malignancies
Acute Myeloid Leukaemia
Acute Lymphoblastic Leukaemia
Chronic Myeloid Leukaemia
Chronic Lymphocytic Leukaemia
what is features of acute leukaemia
Rapidly progressive clonal malignancy of the marrow/blood (myeloid or lymphoid) with maturation defect(s)
defined as an excess of ‘blasts’ in either the peripheral blood or bone marrow
Decrease/loss of normal haemopoietic reserve
what is ALL
malignant disease of lymphocytes
most common childhood cancer
how does ALL present
anaemia, infections, bleeding
- due to marrow failure
high WCC and involvement of extra-medullary areas e.g. CNS,
- leukaemic effects
Bone pain
what are features of AML
more common in the > 60y/o
presentation similar to ALL
Ix for acute leukaemia
1 - blood count and film
2 - coagulation screen
3 - bone marrow aspirate
how will a blood count be in an acute leukaemia
Hb, platelets and neutrophils are LOW
what feature on a blood film would make you think AML
AEUR ROD
what general features on a blood film would make you think Acute leukaemia
reduction in normal
presence of abnormal
“Blasts” with a high nuclear;cytoplasm ratio
what are immunomarkers for: stem cells and myeloid precursors
CD34 = stem cells
CD33 = myeloid precursors
what Ix is needed for a definitive diagnosis of either AML or ALL
Immunophenotyping
how does Tx for acute leukaemia differ
ALL
- lasts up to 2-3 years
- different phases of treatment
AML
- normally intensive
- between 2-4 cycles of chemo
- prolonged hospitalisation
what are complications of Tx
Nausea and vomiting Hair loss Liver, renal dysfunction Tumour lysis syndrome Infection Loss of fertility Cardiomyopathy with anthracyclines
what needs to be done as soon as a neutropenic fever develop
empirical treatment with broad spectrum antibiotics (particularly covering Gram negative organisms)
what is a potential curative Tx for Leukaemia
Allogeneic stem cell transplantation
- get stem cells from a donor
what is philadelphia chromosome
genetic abnormality in chromosome 22 of leukemia cancer cells
= particularly in CML