Introduction To Haematology Flashcards

(48 cards)

1
Q

Where do all blood cells come from

A

Bone marrow

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2
Q

What cells are blood cells derived from

A

Haemopoietic stem cells

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3
Q

What are the site of haemopoiesis during embryogenesis

A

Yolk sac

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4
Q

At birth what is the site for haemopoeisis

A

Bone marrow

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5
Q

In certain condition what is the major site for haemopoiesis

A

Liver

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6
Q

When can you have too few red blood cells

A

Hereditory haemoglobinopathies

Acquired secondary anaemia e.g iron, vitamin b12 or folate deficiency, autoimmune hameolytic anaemia, aplastic anaemia

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7
Q

When can you have too many/dysfunctional

A

Hereditory haemochomatosis due to iron overload

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8
Q

When can you have too few/dysfunctional white cells

A

Rare congenital anaemias
Acquired seconday deficiency- vitamin b12 or folate deficiency, autoimmune neutropenia, aplastic anaemia, drug or viral suppression

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9
Q

When can you have too many white blood cells

A

Myeloproliferative disorders

Acute leukemia

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10
Q

When can you have too few platelets

A

Bone marrow failure syndromes

Acquired secondary deficiency: vitamin b12, folate deficiency, immune thrombocytopenia, drug induce thrombocytopenia

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11
Q

When can you have too many platelets

A

Infection
Trauma
Iron deficiency
Essential thrombocythaemia

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12
Q

When can you have dysfunctional platelets

A

Inherited platelet dysfunction: bernard soulier, glanzmanss

Acquired platelet dysfunction: aspirin, heparin, uraemia

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13
Q

What is contained in plasma

A
Water
Plasma proteins
Electrolyte e.g sodium and chloride
Nutrients: glucose and amino acids
Hormone
Waste: ureea and creatinne 
Gases: oxygen and carbon dioxide
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14
Q

What is the difference between plasma and serum

A

Plasma: liquid part of the blood with no cells that has been treated with anti-coagulants to allow appropiate testing
Serum: liquid part of blood that is coagulated therefore removes fibrinogen (serum=plasma-fibrinogen)

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15
Q

How is a bone marrow examination carried out

A
  1. Patient will lie in a lateral position
  2. Expose the iliac crest
  3. Use a needle to go into the bone marrow cavity
  4. Take a sample of the liquid bone marrrow
  5. Send for an analysis
  6. Then take sample of the periosteum itself called the trephine
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16
Q

What is an aspirate

A

Removal of the liquid bone marrow

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17
Q

What is a trephine

A

Solid histology section and allows study of marrow cellularity

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18
Q

What are exmaples of inherited haemoglobinopathies

A

Thalassemia

Sickle cell disease

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19
Q

What are the 2 types of thalassemia

A

Alpha

Beta

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20
Q

What is beta thalassemia

A

Abnormality of the beta chain

21
Q

What is a feature of the bone marrow compensation of RBC

A

Nucleated red blood cells - the bone marrow is trying to compensate for the anaemia which is pushing out nucleated RBC

22
Q

What is the treatment for beta thalassemia

A

Transfusion

Genetic counselling if they have a child

23
Q

What is alpha thalassemia

A

Abnormality in the alpha gene

24
Q

What are the classification of anaemia by

A

Size of the red blood cell:
Microcytic
Normocytic
Macrocytic

25
What are the causes for microcytic anaemia
Iron deficiency anaemia | Thalassemia
26
What are the causes for normocytic anaemia
Bone marrow failure Aplastic anaemia Chronic disorders Renal disease
27
What are the causes of macrocytic anaemia
B12 and folate deficiency | Alcoholism
28
What are the causes of iron deficiency anaemia
Chronic blood loss: GI bleed or menstruation Poor diet Malabsorption: parasitic infection or GI disease
29
What is the treatment of iron deficiency anaemia
``` Treating the underlying disease Ferrous sulphate (iron tablets) ```
30
What are the causes of macrocytic anaemia
Alcohol | Pernicious anaemia: cant absorb vitamin b12 or folate
31
What are the features of macrocytic anaemia
Pallor | Macroglossia (beef tongue)
32
What are the complicatiomns of macrocytic anaemia
``` Folate deficiency- spina bifida Hypersegmented neutrophils (you can get 5 nuclei of neutrophils) ```
33
What is haemolytic anaemia
This is when the RBC are brocken down rapidly so anaemia occur
34
What is a clinical feature of haemolytic anaemia
Jaundice as RBC breakdown leads to increase in bilirubin
35
What are the causes of haemolytic anaemia
Inherited: membrane, haemoglobin, enzyme Acquired: immune and non immune
36
How does blood clotting occur
1. Endothelium on the blood vessel is damaged 2. VWF binds to the injured vessel wall 4. VWF changes configuration 5. Platelets stick to the VWF 6. GP1B and GP2B/3A will then stick to more platelets can bind
37
What can the pattern on bleedin tell us
Mucosal or skin bleed- vascular or platelet abnormality | Coagulation disorders- bleeding into joints and muscles
38
What can the causes of thrombosis be
Inherited: factor 5 leids, antithrombin, protein c or s abnormality Acquired: vessel damage, stasis, change in blood composition
39
What are the 4 major sets of leukemia
Acute myeloid leukemia Chronic myeloid leukemia Acute lymphoid leukemia Chornic lymphoid leukemia
40
What are lymphomas
Tumours of lymphocytes- commonly in b than t
41
Give examples of lymphoma
Non hodgkin lymphoma | Hodgkin lymphome
42
What does hodgkin lymphoma in histology show
Owl eye
43
What is myeloma
Maligancy of the plasma cells that produce a monoclonal immunoglobulin called paraprotein
44
What is myeloma likely to present with
Renal failure Bone pain Anaemia Infection
45
In transfusion what can we give
``` Packed red blood cells Platelets Fresh frozen plasma and cryoprecipitate Fresh frozen plasma Cyroprecipitate ```
46
What is in the packed red blood cells
Platelts and plasma are removed just the RBC
47
What does fresh frozen plasma contain
Coagulation factors
48
What does cyroprecipitate contain
Factor 8,13,vwf and fibrinogen