Physiology of blood cells and haematological terminology Flashcards

(50 cards)

1
Q

Where do blood cells of all types originate?

A

In the bone marrow

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2
Q

What are all blood cells ultimately derived from?

A

Pluripotent haematopoietic stem cells

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3
Q

What do pluripotent haematopoietic stem cells give rise to?

A

Lymphoid stem cells

Multipotent myeloid stem cells/precursors

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4
Q

What do erythrocytes originate from?

A

Multipotent haematopoietic stem cell –> multipotent myeloid stem cell/precursor –> proerythroblast –> erythroblast –> erythrocyte

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5
Q

What are the functions of erythrocytes?

A

Oxygen transport

Some carbon dioxide transport

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6
Q

What is the approximate intravascular life span of an erythrocyte?

A

120 days

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7
Q

What do white cells originate from?

A

Multipotent haemopoietic stem cell –> multipotent myeloid stem cell/precursor –> myeloblast –> granulocytes, monocytes

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8
Q

What do monocytes and granulocytes need for further differentiation?

A
Cytokines:
G-CSF - granulocyte colony stimulating factor
M-CSF - macrophage
GM-CSF
Various interleukins
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9
Q

What is the approximate intravascular life span of a neutrophil?

A

7-10 hours

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10
Q

What is the function of neutrophils?

A

Defence against infection

Phagocytoses and kills MOs

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11
Q

What is the approximate intravascular life span of a eosinophil?

A

Less than 7 hours (less than a neutrophil)

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12
Q

What is the function of eosinophils?

A

Defence against parasitic infection

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13
Q

What is the approximate intravascular life span of a monocyte?

A

Several days

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14
Q

What are the functions of monocytes?

A

Migrate into tissues and develop into macrophages and other specialised cell types w/phagocytic function
Store and release iron

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15
Q

What is the approximate intravascular life span of a platelet?

A

10 days

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16
Q

What are the functions of platelets?

A

Primary haemostasis

Contribute phospholipid in blood coagulation

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17
Q

What do platelets originate from?

A

Multipotent haemopoietic stem cell –> multipotent myeloid stem cell/precursor –> megakaryocytes –> platelets

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18
Q

What do lymphocytes originate from?

A

Multipotent haemopoietic stem cell –> lymphoid stem cell –> T, B, NK cells

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19
Q

What is the approximate intravascular life span of a lymphocyte?

A

Very variable

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20
Q

What is anisocytosis?

A

Red cells show more variation in size than is normal

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21
Q

What is poikilocytosis?

A

Red cells show more variation in shape than is normal

22
Q

What is microcytosis?

A

Smaller red cells than normal or an anaemia with small red cells

23
Q

What is macrocytosis?

A

Larger red cells than normal or an anaemia with large red cells

24
Q

What is hypochromia? What causes it?

A

Cells have a larger area of central pallor than normal (normally 1/3 of diameter)

Lower haemoglobin content and concentration + flatter cell

25
What is hyperchromia? What causes it?
Cells lack central pallor | Bc thicker than normal or shape is abnormal
26
What are 2 important types of hyperchromic cells? What causes them?
Spherocytes - loss of CM w/o loss of equivalent amount of cytoplasm - hereditary spherocytosis Irregularly contracted cells - oxidant damage to CM and Hb
27
What is polychromasia? What causes it?
Increased blue tinge to the cytoplasm of a red cell As red cells mature, they go from dark blue --> pink Indicates that red cells are young (reticulocytes) - not fully matured
28
What shapes can red cells be?
``` Spherocyte Irregularly contracted cell Sickle cell Target cell Elliptocyte Fragment ```
29
What are the differences between Rouleaux and agglutinates?
Rouleaux = neat stacks of red cells due to increased levels of plasma proteins Agglutinates = irregular clumps of red cells due to antibodies on cell surface
30
What is Howell-Jolly body? What is the most common cause?
Nuclear remnant in a red cell Lack of splenic function Spleen should remove these tiny remaining bits of nuclear material
31
What is a target cell? When do they occur?
Red cell with accumulation of haemoglobin in middle of central pallor Obstructive jaundice, liver disease, haemoglobinopathies, hyposplenism
32
What is an elliptocyte? When do they occur?
Elliptical and hypochromic red cell | Hereditary elliptocytosis and iron deficiency
33
What are fragments? What do they indicate?
AKA schistocytes Small pieces of red cells - tend to have red cell colour and central pallor, just shape is different Indicate fragmented red cells
34
What is leucocytosis?
Too many white cells
35
What is leucopenia?
Too few white cells
36
What is neutrophilia?
Too many neutrophils (may be normal in infection)
37
What is neutropenia?
Too few neutrophils
38
What is lymphocytosis?
Too many lymphocytes
39
What is eosinophilia?
Too many eosinophils
40
What is thrombocytosis?
Too many platelets
41
What is thrombocytopenia?
Too few platelets
42
What is erythrocytosis?
Lots of red blood cells
43
What is reticulocytosis?
Lots of reticulocytes
44
What is lymphopenia?
Reduced number of lymphocytes
45
What do lymphocytes typically look like?
Small and round Large nucleus Little cytoplasm
46
What does an atypical lymphocyte typically look like?
Large and very visible nucleus Loads of really faint cytoplasm Note: typical of viral infection
47
What is left shift? What does it suggest?
Increase in non-segmented neutrophils or presence of neutrophil precursors in the blood Band form neutrophils present in blood film Suggests infection or inflammation - BM releasing lymphocytes earlier than normal
48
What is toxic granulation?
Heavy granulation of neutrophils due to infection, inflammation or tissue necrosis (or normal pregnancy)
49
What is a hypersegmented neutrophil?
A neutrophil with an increased number of nucleus lobes or segments
50
What are sickle cells? What is the cause?
Sickle/crescent shaped red cells due to polymerisation of HbS when present in high concentration