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Culture Documents
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