Concepts in haematology Flashcards

(41 cards)

1
Q

what are causes of low blood count

A

increased destruction/loss: haemorrhage, haemolysis
reduced production: chemo, parovirus B19
redistribution: liver disease, portal hypertension, splenomegaly

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2
Q

what are causes of high blood count

A

increased production with stimulus: infection, hypoxia, high altitude, COPD
increased production with no stimulus: malignancy
redistribution: steroids

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3
Q

-cytosis / -philia = high/low count

A

high

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4
Q

-paenia = high/low count

A

low

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5
Q

what is the difference between thrombocytosis and thrombophilia

A
thrombocytosis = increased platelets 
thrombophilia = excess clotting
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6
Q

what underlying malignancies may be present with an isolated thrombocytosis

A
LEGO C
lung 
endometrial 
gastric 
oesoophageal 
colorectal
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7
Q

define hyperplasia

A

increased production

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8
Q

define dysplasia

A

disordered production

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9
Q

define hypoplasia

A

decreased production

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10
Q

define aplasia

A

no production

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11
Q

what is the erythron

A

intact cellular mechanism generating RBCs

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12
Q

what are reticulocytes

A

immature RBC just released into the bloodstream from bone marrow

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13
Q

what is the function of B12 and folate

A

cell division: DNA synthesis and nuclear maturation

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14
Q

what is the function of iron

A

to make haem

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15
Q

which organ detects hypoxia

A

kidneys

release EPO in response

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16
Q

what is erythroid hyperplasia

A

increased production in RBCs

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17
Q

thrombocytosis is common with microcytic anaemia, true or false

18
Q

what is low serum ferritin suggestive of

A

iron deficiency

19
Q

what is serum ferritin

A

an indirect reflection of tissue ferritin which stores Fe3+

ferritin is also an acute phase protein

20
Q

causes of high serum ferritin

A

high iron levels

inflammation, infection

21
Q

how can you assess response to iron replacement therapy in iron deficiency anaemia

A

reticulocyte count should increase

Hb levels

22
Q

what is extramedullary haematopoeisis

A

blood cell production outside the bone marrow

23
Q

what is a complication of regular blood transfusions

A

iron overload

24
Q

what are spherocytes

A

circular RBCs, not biconcave in shape

25
what is hereditary spherocytosis
genetic condition with abnormal proteins in RBC membrane resulting in spherical shape jaundice and fatigue following a cold
26
what investigations can be done for haemolysis
``` FBC bilirubin - high LDH - marker of cell turnover Haptoglobin - binds free Hb reticulocytes - high antibodies by DAT ```
27
Haptoglobin is low/high in haemolysis, and why
low haptoglobin binds free iron, if there is a lot of iron from haemolysis then a lot of haptoglobin is used up meaning FREE haptoglobin is low
28
what is IAT testing
indirect anti-globulin test | - used for crossmatching
29
what is DAT
direct anti-globulin test | - autoimmune haemolytic anaemia
30
spherocytes have a shorter lifespan, true or false
true
31
splenectomy increases/decreases RBC lifespan
increases | the spleen is where RBC are destroyed, if it is not there, they hang around for longer
32
risks of splenectomy/hyposplenism
infection and immunosuppresion risks of clots big operation need vaccinations before
33
What is meant by reactive changes on the blood count
from underlying inflammatory changes or iron deficiency you can get neutrophilia, leucocytosis, thrombocytosis
34
What can cause a high Hb/Hct
dehydration (rule out hypovolaemia, DKA, diuretics) cigarette smoking high altitude COPD
35
what is anisocytosis
how large red cell distribution width is (RDW)
36
causes of neutrophilia
``` steroids smoking trauma infection malignancy ```
37
what is rouleaux
stacked/clumped RBCs due to presence of acute phase proteins in inflammatory conditions eg autoimmune
38
what is pancytopaenia
reduced blood cells all over
39
what is anisopoikilocytosis and in which condition is it seen
red blood cells are of different sizes and shapes aniso = size poikilo = shape B thalassaemia major
40
what are crenated red cells (echinocytes)
abnormally contracted cells - look shrivelled (eg when placed in a hypertonic solution) PK deficiency drugs
41
why do you get splenomegaly
presence of defective cells causes them to be destroyed which is done in the spleen - hyperplasia at site of destruction extravascular haemolysis thalamssaemia