Haemotology Flashcards

1
Q

what are the components of blood?

A

55% Plasma - water, proteins, other solutes

45% Cells - red blood cells
white blood cells (lymphocytes, granulocytes, monocytes)
platelets

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2
Q

What is the name of blood cell production?

Where are blood cells made?

A

Haematopoiesis

Before birth by yolk sac and then spleen/liver. By adulthood it is mainly axial skeleton (vertebrae and pelvis) in bone marrow

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3
Q

What percentage of marrow production is white cells/red cells?

Precursor for platelets?

A

75% white cells
25% red cells

Megakaryocytes are platelet producing cells

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4
Q

What is the stem cell which gives rise to all other blood cells?

What are the two lineages of blood cells and which cells do they produce?

A

Haematopoeitic stem cells (HSC)

Myeloid: erythrocytes, platelets, granulocytes (eosinophils, neutrophils, basophils), monocytes (macrophages)
Lymphoid: Mature in thymus - T cell, B cell, NK cells

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5
Q

Which growth factors are used to stimulate differentiation of erythrocytes? Platelets? Granulocytes?

A

Erythrocytes - erythropoietin (EPO) produced by the kidney is response to anaemia or hypoxia

Platelets - thrombopoietin (TPO) produced by liver

Granulocytes - granulocyte colony stimulating factor (G-CSF)

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6
Q

What is the MCV (mean cell volume) and what is it useful for measuring?

A
Mean cell volume measures the red cell volume (size)
Normal range (normocytic) is 80-100fL. 
Starting point for evaluation of anaemia
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7
Q

Cause of:
microcytic anaemia
macrocytic anaemia

A

microcytic anaemia- small cells, cause: iron deficiency

Macrocytic - large cells, cause: folate deficiency

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8
Q

Reticulocyte count

A

‘RBC to be’
increased reticulocyte numbers = increased RBC production

If reticulocytes are reduced, then problem with production (anaemia)

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9
Q

Describe plasma cells.

Is reactive increase clonal or polyclonal?

A

Part of humoral immunity. Plasma cells produce antibodies or immunoglobulins. Immunoglobulins have a constant and variable reigon.

Reactive increase is POLYCLONAL

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10
Q

What is polycythaemia and what are the types?

A

Increased Hb and Hct.

Relative polycythaemia: Due to decrease in plasma. No change in absolute RBC mass but propotionate increase. Dehydration, diuretics, alcohol

Absolute polycythaemia: Increase in RBC mass

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11
Q

Causes of primary and secondary polycythaemia

A

Primary (neoplastic): Polycythaemia ruba vera, myeloproliferative disorder, JAK2 mutated, EPO suppressed

Secondary: JAK2 unmutated, EPO increased (hypoxia, smoking, high altitude, tumours)

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12
Q

Causes of Thrombocytosis (increased platelets)

A
1. Reactive: 
Trauma (e.g. by surgeon)
Infection
Inflammation
Splenectomy 
Iron deficiency 
Non-haemotlogical malignancy
2. Clonal
Myeloproliferative disorders (MPN)
  1. Spurious (FBC machine counts something else as platelets)
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13
Q

Causes of Leucocytosis (increased white cells)

A
1. Reactive
Trauma (e.g. by surgeon)
Smoking
Infection
Inflammation
Non-haemotological malignancy
splenectomy 
steroids
  1. Clonal
    lymphoproliferative, myeloproliferative
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14
Q

Causes of lymphadenopathy

A

Infection: viral (HIV/EBV) or bacterial (TB)
Non haemotological cancer
Inflammatory (Sarcoid, SLE)
Lymphoproliferative neoplasms

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15
Q

Acute Leukaemia

Types? presentation?

A

AML: acute myeloid leukaemia
ALL: acute lymphoblastic leukaemia

Proliferation of immature cells

Present with bone marrow failure i.e anemia, thrombocytopaenia (bleeding), neutropenia (infection)

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16
Q

Myeloproliferative Neoplasms

  • characterised by?
  • cause?
  • result?

Types for granulocytes? red cells? Platelets?

A

Characterised by excessive proliferation of terminally differentiated myeloid cells (cells look normal)

Caused by somatic mutation of haematopoetic stem cells.

Leads to cytokine independent growth

Granulocytes - chronic myeloid leukaemia

Red cells - ruba vera polycythaemia

Platelets - Essential thrombocythaemia

17
Q

Lymphoproliferative neoplasms

Types?

A

B cell or T cell

Leukaemia: bone marrow>lymph nodes

Lymphona: lymph nodes>bone marrow
Hodgkin’s lymphoma
Non Hodgkin’s lymphoma

18
Q

Clonal plasma cells (neoplastic plasma cells)
How do the not present?
What does it cause?

A

Does not present with peripheral blood plasmacytosis or lymphadenopathy (cells accumulate in bone marrow)

Plasma cells produce abnormal, ineffective immunoglobulin which leads to decreased bone marrow function, destruction of bone tissue and end organ damage

19
Q

What is shown in an abnormal serum electophoresis result for myeloma?

A

M spike

20
Q

What are symptoms of Myeloma?

A
CRABI
C - hypercalcaemia 
R- renal dysfuntion
A- anaemia
B- bone (leisons, osteoporosis, fractures
I - infection
21
Q

Thrombocytopenia (low platelets) causes

A

Immune - immune thrombocytopenia (lymphoproliferative HIV or hepatitis C infection)

Drugs - heparin, anticonvulsants, chemotherapy, alcohol, quinine

Infections

Marrow dysfunction - dysplasia, infiltration, aplasia, fibrosis

Liver disease

Splenomegaly

Microangiopathic haemolysis

Preganancy specific- gestational, HELLP syndome

22
Q

Neutropenia (low neutrophils) causes

A

Drugs - antipsychotics, anticonvulsants, chemotherapy, omeprazole

Infections

Marrow dysfunction - dysplasia, infiltration, aplasia, fibrosis

Immune

Splenomegaly