Hypercalcemic crisis
Multiple myeloma
Microcytic anaemia with normal RDW?
Beta-thalassemia
Microcytic anaemia with high RDW?
Iron deficiency anaemia
Blood film for thalassemia?
Heinz bodies (alpha)
Basophilic stippling
Target cells
What condition has tear-drop poikilocytes?
Myelofibrosis
Presentation of hereditary spherocytosis?
Failure to thrive Jaundice, gall stones Splenomegaly Aplastic crisis precipitated by parvovirus infection CHC elevated
Hereditary spherocytosis?
Autosomal dominant Extravascular haemolysis Neonatal jaundice Gallstones Northern European
G6PD deficiency?
X linked recessive
African-Mediterranean
Intravascular haemolysis
Blood film of G6PD?
Heinz bodies
Increased reticulocytes
Blood film of hereditary spherocytosis?
Spherocytes - round, lack of central pallor
How to diagnose hereditary spherocytosis?
Abnormal blood film + family history + raised MCHC
EMA binding test
How to diagnose G6PD?
Measure enzyme activity
Causes of massive splenomegaly?
Myelofibrosis Chronic myeloid leukaemia Visceral leishmaniasis Malaria Gaucher's syndrome
What is gaucher’s syndrome?
Accumulation of glucocerebroside in cells and organs Fatigue Anaemia Low platelet Hepatosplenomegaly
Haemophilia A?
X linked recessive
Factor VIII deficiency
Haemophilia B?
X linked recessive
Factor IX deficiency
Features of haemophilia?
Prolonged APTT
Normal thrombin time
Normal prothrombin time
Blood film for CLL?
Smudge/smear cells
Blood film for AML?
Auer rods
What is chronic lymphocytic leukaemia?
Monoclonal proliferation of well differentiated lymphocytes, almost always B cells
Features of CLL?
Often none Anorexia Weight loss Bleeding Infection Lymphadenopathy
Complication of CLL?
Anaemia
Hypogammaglobulinemia
Warm autoimmune haemolytic anaemia
Transformation to high grade lymphoma
What is Richter’s transformation?
CLL to high grade lymphoma
Normocytic anaemia?
Anaemia of chronic disease Chronic kidney disease Aplastic anaemia Haemolytic anaemia Acute blood loss