Haematology Flashcards

(56 cards)

1
Q

when might MCV be normal in anaemia?

A
  • normocytic anaemia

- mixed microcytic AND macrocytic anaemia

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2
Q

causes of microcytic anaemia?

A
  • Fe def
  • chronic disease
  • thalassaemia
  • sideroblastic anaemia
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3
Q

causes of macrocytic anaemia?

A
  • B12 def
  • folate def
  • XS alcohol
  • reticulocytosis
  • hypothyroidism
  • multiple myeloma
  • myeloproliferative disorders
  • myelodysplasia
  • aplastic anaemia
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4
Q

causes of normocytic anaemia?

A
  • chronic disease
  • haemolytic anaemia
  • acute blood loss
  • marrow infiltration
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5
Q

where is iron absorbed? which form is it in when it gets absorbed?

A
  • upper small bowel

- ferrous (Fe2+)

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6
Q

what are the components of an iron profile?

A
  • serum iron
  • serum TIBC
  • serum ferritin
  • transferrin saturation
  • serum soluble transferrin receptors
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7
Q

describe the iron profile for someone who is iron deficient

A
  • low serum iron
  • high TIBC
  • low serum ferritin
  • low transferrin
  • high transferrin receptors
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8
Q

what is the single best blood marker for iron deficiency?

A
  • serum ferritin

- (but be careful bc it’s also an acute phase reactant)

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9
Q

what might cause iron overload?

A
  • haemochromatosis

- frequent blood transfusions

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10
Q

describe the iron profile of someone with iron overload

A
  • high serum iron
  • high ferritin
  • high transferrin
  • low TIBC
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11
Q

describe the iron profile in anaemia of chronic disease (ACD)

A
  • normal / low serum iron
  • low TIBC
  • low transferrin
  • high ferritin (if inflammation)
  • normal transferrin receptors
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12
Q

give an example of ileal disease which could lead to B12 def. how could this be diagnosed?

A
  • small bowel bacterial overgrowth
  • trialling ABx and then checking B12 levels
  • hydrogen breath test
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13
Q

how can hereditary spherocytosis be tested for? what happens?

A
  • osmotic fragility test

- spherocytes are fragile and breakdown more easily

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14
Q

how can autoimmune haemolytic anaemia be tested for? what happens?

A
  • direct antiglobulin test (DAT) / coombs’ test

- the cells agglutinate (stick together)

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15
Q

how can haemolytic anaemia be classified?

A
  • inherited

- acquired

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16
Q

examples of inherited causes of haemolytic anaemia?

A
  • spherocytosis
  • thalassaemia
  • SCA
  • G6PD
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17
Q

examples of acquired IMMUNE causes of haemolytic anaemia?

A
  • autoimmune warm type
  • autoimmune cold type
  • transfusion reaction
  • HDN
  • adverse drug event
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18
Q

examples of acquired NON-IMMUNE causes of haemolytic anaemia?

A
  • malaria
  • hypersplenism
  • burns
  • mechanical heart valve
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19
Q

how can polycythaemia be classified?

A
  • apparent (low blood volume making RBC look high)

- true

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20
Q

key cause of apparent polycythaemia?

A

dehydration

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21
Q

underlying disease which could give polycythaemia?

A

polycythaemia rubra vera

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22
Q

secondary causes of polycythaemia?

A
  • lung disease
  • chronic smoking
  • high altitude environment
  • renal cell carcinoma
  • polycystic kidneys
  • HCC
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23
Q

causes of neutrophilia?

A
  • bacterial infection
  • inflammation
  • malignancy
  • myeloproliferative disorders
  • post-MI
  • corticosteroid use
  • renal failure
24
Q

causes of neutropenia?

A
  • post-chemo
  • post-radio
  • clozapine / carbimazole use
  • viral infection
  • felty syndrome (along with RA and splenomegaly)
25
causes of lymphocytosis?
- viral - chronic infections (TB) - CLL - lymphoma
26
causes of eosinophilia?
- allergic disorders - parasitic infection - eczema and other skin stuff - hodgkin's disease and other malignancies
27
causes of thrombocytosis? (non-reactive)
- essential thrombocythaemia - CML - myelodysplasia
28
causes of reactive thrombocytosis?
- infection / inflammation - malignancy - bleeding - pregnancy - post-splenectomy
29
causes of thrombocytopenia relating to bone marrow failure?
- infectious mononucleosis - drug-induced - leukaemia - aplastic anaemia - myelofibrosis - myeloma / bony mets (BM infiltration) - myelodysplasia - megaloblastic anaemia
30
causes of thrombocytopenia relating to increased platelet destruction?
- autoimmune idiopathic thrombocytopenia (AITP) - heparin-induced thrombocytopenia (HIT) - hypersplenism - TTP / HUS - DIC - post-blood transfusion
31
causes of pancytopenia?
- aplastic anaemia - myeloma / bony mets (BM infiltration) - hypersplenism - megaloblastic anaemia - sepsis - SLE
32
what is pancytopenia?
low RBCs, WCC and platelets
33
causes of a raised ESR?
- infectious disease - multiple myeloma - GCA, PMR - anaemia - renal disease
34
when are acanthocytes seen on blood film?
- post-splenectomy | - liver disease
35
when are target cells seen on blood film?
- thalassaemia - iron deficiency - post-splenectomy - liver disease
36
when are burr cells seen on blood film?
- post-splenectomy - liver disease - uraemia
37
when are fragmented cells seen on blood film?
- haemolytic anaemia - HUS - TTP - mechanical heart valves - DIC
38
when are "tear drop" cells seen on blood film?
myelofibrosis
39
what kinds of abnormalities can be seen inside RBCs on blood film?
- heinz bodies - howell-jolly bodies - pappenheimer bodies - basophilic stippling - cabot rings
40
which conditions can cause heinz bodies to form?
any unstable state of Hb
41
which conditions can cause howell-jolly bodies to form?
- hyposplenism | - post-splenectomy
42
which conditions can cause pappenheimer bodies to form?
- post-splenectomy - haemolytic anaemia - sideroblastic anaemia
43
which conditions can cause basophilic stippling to form?
- lead poisoning - thalassaemia - myelodysplasia
44
which conditions can cause cabot rings to form?
- myelodysplasia | - megaloblastic anaemia
45
what kinds of abnormalities can be seen inside WBCs?
- hypersegmented neutrophils - toxic granulation of neutrophils - auer rods - smear cells
46
which conditions can cause hypersegmented neutrophils to form?
- megaloblastic anaemia | - chronic infection
47
which conditions can cause toxic granulation of neutrophils to form?
- bacterial infection - poisoning - burns - chemotherapy
48
which condition can cause auer rods to form?
AML
49
which condition can cause heinz bodies to form?
CLL
50
what is the most effective blood test to assess liver function?
prothrombin time (PT)
51
when should a pt have a target INR of 3.5 (3-4)?
where there is recurrent DVT / PE in a pt with a therapeutic INR
52
what might bloods show in DIC?
- high PT and APTT - low fibrinogen - high D-dimer
53
what is APTT used for most commonly?
to monitor a heparin infusion
54
causes of bleeding where INR is raised?
- warfarin - heparin (sometimes) - liver disease - DIC
55
causes of bleeding where APTT is raised?
- heparin - haemophilia A / B - liver disease - DIC
56
give a cause of bleeding where fibrinogen is affected. what happens?
- DIC | - it drops