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ANAEMIA

Blood Loss

MCV
-

Blood Film
reticulocytes

Megaloblastic

Oval Macrocytes
Hyper-segmented neutrophils
Ansio/poikilocytosis
Tear Drops
May have WCC and platelets

Iron Deficiency

Hypochromic microcytic
Target Cells

Haemolysis

Spherocytes
Reticulocytes

Hx
Shock, trauma,
haemorrhage,
melena,
menorrhagia
Diet
Surgery
Jaundice
Bruising
Infections
Autoimmune
growth
Angular
stomatitis
Glossitis
Koilonychia
Diet, Surgery
Jaundice
Splenomegaly

Ix
Iron deficiency
Cause of bleeding
WCC and Platelets

Mx
Treat
cause of
bleeding

Folate
B12 Levels
Anti-IF and anti-parietal cell Ab
Signs of ineffective erythropoiesis
bilirubin and LDH

Replace
B12 or
Folate

Iron Studies
Serum Fe
Serum transferrin
Saturation

Replace
Iron

Ferritin
Bilirubin + LDH
Haptoglobin (binds Haem)
Coombs Test anti-RBC Ab

LEUKAEMIAS
Type
ALL
Typically occurs in
childhood
Majority are B cell
AML
Late adulthood

Morphology
Clumped Chromatin
Scant cytoplasm
No granules
Inconspicuous nucleoli
Delicate chromatin
Much cytoplasm
Fine granules
Auer rods

ImmunoPhenotyping
B lineage TdT,
CD19, CD10
T linage CD7,
CD3m TdT
Myeloid CD33,
CD13

Cytogenetics
T(9,22) Ph
chromosome
BCR-abl tyr kinase)
AMPL = t(15,17)
RAR-PML treat
with ATRA

Chronic Leukaemia
CML

CLL

Clinical Features
Often incidental finding
Splenomegaly
Low or high platelet count
High WCC hyperviscosity
numbers of myeloid cells ranging from
blasts to mature cells in blood and bone
marrow
Incidental finding
Lymphadenopathy, Hepatosplenomegaly
Bone marrow failure pancytopenia
Autoimmune complications
Peripheral blood contains high numbers of
small, round lymphocytes with scant
cytoplasm fragile smudge cells
numbers lymphocytes in bone marrow

Diagnosis
Philadelphia Chromosome
Average survival = 4 years

Immunophenotyping CD5 +
CD19 and surface kappa or
lambda
Identify lymphocytosis as due to
the clonal expansion of a single
cell
Average survival = 6-8 years

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