What is anaemia?
Haemoglobin outside the reference range for the normal population.
What are the signs and symptoms of anemia?
Symptoms: shortness of breath tiredness, cardiac failure, palpitations, headache
Signs: pallor, tachycardia, tachypoea, hypotension
What are some specific signs of amemia?
Koilonychia (spoon nails)
Glossitis (inflammation of the tongue)
Oesophageal webs (webs along the oesophagus)
Angual stomatitis (inflammatory condition affecting the corners of the mouth)
Thalassaemia - Abnormal facial bone development.
What is the physiological life cycle of a RBC?

Why might anaemia develop?
Problems with:
why would a patient have reduced erythropoiesis?
What is dyserythropoiesis?
This is anaemia of inflammation or anaemia of chronic disease.
Iron is not released for use in the bone marrow which leads to a reduced lifespan of red cells. This means the marrrow shows a lock of response to erythropoietin.
This is seen in renal disease. RA, SLE, inflamatory bowel diesease, or other chronic infections.
What could cause defcts in haemoglobin synthesis?
Deficiencies in things that are essential:
What inherited defects cause changes in the structure of red cells?
Abnormalities of the proteins making up the red cellmembrane can lead to anaemia.
The cells in there conditions are less flexible and are damaged more easy. This means they break up and are removed from circulation.
What can cause aquired defects in the red cell membrane structure?
Mechanical damage to red cells including:
Heat damage
Osmotic change
How can defects in red cell metabolism lead to anaemia?
Red cell enzyme defects can lead to haemolytic anaemia. The best recognised defects are:
How does the reticuloendothelial system lead to anaemia?
The RES removes an excess of damaged red cells.
The spleen removes damaged or defective red cells in a variety of causes of amaemia (membrane, enzyme and Hb disorders). In haemolytic anaemia, red cells are destroyed more quickly as they are abnormal or damaged.
This removal can be intravascular or extravascular.
What are the causes of incresed reticulocytes?
Acute blood loss
Splenic sequestration
Haemolysis (immume or non immune mediated)
What are the causes of low reticulocute count?
Low MCV
TAILS!
High MCV
Vit B12, Folate, Myelodysplasia, Liver disease, Hypothyroidism, Alcohol
Normal MCV
Primacy bone marrow failure (rare) -aplastic anaemia and red cell aplasia
Secondary bone marrow failure - anaemia of chroic disease, Combined haematinic deficiencies, Uraemia, Endocrine abnormalities, HIV infection.
MCV = mean cell volume.
What does vit B12 or folate deficiency cause?
Vitamin B12 and/or folate deficiency causes deficiency in building blocks for DNA synthesis.
The causes megaloblastic anaemia.
This is the most common cause of macrocytic anaemia.
Where is B12 found?
Animal products
How does B12 get absorbed?
B12 binds with haptacorrin which is secreted by the salivary glands.
The B12-Haptacorrin pretects the B12 in the stomach.
In the stomach, the patietal cells produce HCl and intrinsic factor.
Then, B12 and haptacorrin and intrinsic factor both pass into the small intestine.
In small intestine, haptacorrin B-12 complex breaks apart and the B-12 binds to intrinsic factor.
B-12 intrinsic factor complex move into theterminal ilium.
Here, B-12 is absorbed into the portal blood though the wall and IF gets distroyed.
In the blood, it binds to a protein called transcobalamine II.
This is the mainly stored in the liver then carried to the places required.
How long would body stored of vitamin B-12 last?
We have body stores of B-12 as eat lots of meat, fish eggs and cheese. These stores could last 3-6 years. This means that it takes a long time to become B-12 deficient.
What are the causes of B-12 deficiencies?
What is folate?
Folate is present in most foods, year, liver and leafy greens are an especially rich source.
Stores can only last for about 3-4 months.
Absorbtion occurs in the duodenum and jejunum.
What could cause folate deficiency?
What do B-12 and folate do?
Dietary folates are all converted to methytetrahydrofolate (methylTHF) which is the ‘functional form’
B-12 removes the methy groupt from methylTHF to form THF.
THF is essential for a variety of reactions but, most importantly, it is essential for synthesising thymidylate (thymidine/thymine) which is essential for synthesising DNA.
So, if no B-12, you can’t remove the methyl group and therefore make thymidine.
This means that lack of B-12 results in a functional folate deficiency but lack of folate results in an actual folate deficiency.
Why do B-12 ad folate deficinecy cause megaloblastic anaemia?