Haematology Flashcards

1
Q

Acanthocytes

A

Spike rbc

Seen in liver disease and hyposplenism

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2
Q

Basophilic RBC stippling

A

Accelerated erythropoiesis or defective Hb synthesis

Due to lead poisoning, liver disease and thalassaemia

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3
Q

Burr cells

A

Irregularly shaped cells

Uraemia, GI bleed or stomach cancer

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4
Q

Heinz bodies

A

Denatured Hb inclusion in RBC

G6PD deficiency or chronic liver disease

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5
Q

Howell Jolly body

A

Basophilic nuclear remenant in RBC

Seen in hyposplenism ie sickle cell or coeliacs

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6
Q

Leucoerythroblastic anaemia

A

Nucleated RBC and primitive WBCs due to marrow infiltration

Seen in myelofibrosis

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7
Q

Pelger Heut cells

A

Hyposegmented neurtrophils

Myelodysplastic syndromes

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8
Q

Reticulocytes

A

Mesh like network of rRNA visible with methylene blue

Increased in haemolytic anaemia

Decreased in aplastic anaemia and chemotherapy

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9
Q

Right shift

A

Hyper mature WBCs with more than five lobes

Seen in megaloblastic anaemia, uraemia and liver disease

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10
Q

Rouleaux formation

A

Stacked RBCs

Seen in myeloma and paraproteinaemia

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11
Q

Schistocytes

A

Fragmented RBCs

Due to microangiopathic anaemia - DIC, haemolytic uraemia syndrome, thrombotic thrombocytopenic purpura

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12
Q

Target cells

A

Bulls eye appearance

Seen in liver disease, hyposplenism, iron deficiency anaemia and thalassaemia.

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13
Q

Blood Hb levels below which one is considered anaemic for:

  • men
  • women
A

Men <13.5g/dl

Women < 11.5g/dl

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14
Q

Causes of a low MCV and anaemia (4)

A

Fe deficiency
Anaemia of chronic disease
Sideroblastic
Thalassaemia

=FAST

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15
Q

Anaemia and high MCV (7)

A
Foetus 
Antifolates - phenytoin 
Thyroid (low)
Reticulocytosis 
B12/folate deficiency 
Cirrhosis 
Myelodysplastic syndromes 

=FAT RBCM

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16
Q

A 45 year old lady with brittle hair and angular cheilosis.

Blood film shows hypochromatic anisocytosis and pencil cells

A

Iron deficiency anaemia

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17
Q

Poikilocytosis and pencil cells are seen in what

A

Iron deficiency anaemia

18
Q

Causes of iron deficiency anaemia (5)

A
Blood loss 
Increased utilisation - pregnancy or lactation
Decreased intake
Decreased absorption - coeliac
Intravascular haemolysis 

NB it is bleeding until proven otherwise in the acute setting

19
Q

Two mechanisms behind anaemia of chronic disease.

A

Cytokines driven RBC production inhibition
1. TNF/IFNs cause a decrease in production of EPO receptors –> decrease in kidney EPO production

  1. IL6/LPS cause an increase in liver hepcidin production –> decreased gut iron absorption and increased macrophage iron levels
20
Q

What is sideroblastic anaemia and what causes it?

A

Ineffective erythropoeisis leading to iron loading in the bone marrow –> endocrine, liver and cardiac damage

Due to myelodysplasia, chemotherapy, excess alcohol or myeloproliferative disease

21
Q

Low iron, high total iron binding capacity and low ferritin

A

Iron deficiency anaemia

22
Q

Low iron, low total iron binding capacity and raised ferritin

A

Anaemia of chronic disease

23
Q

High iron, low total iron binding capacity and high ferritin

A

Chronic haemolysis

24
Q

High iron and high ferritin

A

Haemochromatosis or sideroblastic anaemia

25
What is ferritin?
Acute phase protein therefore levels increase with inflammation NB always check the CRP
26
Three causes of vitamin B12 deficiency
Poor diet Malabsorption due to lack of intrinsic factor from the gastric parietal cells - pernicious anaemia Loss of the terminal ileum - Crohn's disease, resection
27
Patient with absent ankle reflexes, anaemia and glossitis
Vitamin b12 deficiency
28
Treatment for vitamin b12 deficiency
I.m. Hydroxocobalamin
29
Autoantibody in pernicious anaemia
90% parietal cell antibodies
30
Five causes of folate deficiency
Poor dietary intake Increased demand - pregnancy Increased cell turnover - haemolysis/inflammatory disease Malabsorption - coeliacs Drugs - phenytoin/methotrexate/alcohol/trimethoprim
31
Normal RBC lifespan
120 days
32
Raised unconjugated bilirubin, raised LDH and reticulocytosis
Haemolytic anaemia
33
Three inherited causes of haemolytic anaemia
Membrane defect - hereditary spherocytosis Enzyme defect - G6PD, pyruvate kinase deficiency Haemoglobinopathies - sickle cell
34
Two acquired causes of haemolytic anaemia
Immune - cold/warm or transfusion reaction Non-immune - mechanical/MAHA
35
Inheritance of hereditary spherocytosis
Autosomal dominant
36
Deficiency which results in hereditary spherocytosis
Ankyrin or spectrin membrane protein deficiency
37
Key investigation to identify hereditary spherocytosis
Osmotic fragility
38
Inheritance of G6PD
X linked
39
Rapid anaemia, bite cells and Heinz bodies in previously well individual
G6PD
40
Triggers for G6PD attacks
Oxidants i.e. Sulphonamides, aspirin, primaquine or broad beans
41
Severe neonatal jaundice, splenomegaly and a haemolytic anaemia which is Coombs negative
Pyruvate kinase deficiency