Introduction to Haematology Flashcards

1
Q

label the components of blood

A
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2
Q

how is anaemia classified?

A

anaemia = low Hb

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3
Q

what are some causes for microcytic anaemia?

MCV < 78fL

A
  • iron deficiency anaemia
  • haemoglobinopathies e.g. thalassaemia
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4
Q

what are some causes for normocytic anaemia?

MCV 78-98 fL

A
  • anaemia of chronic disease
  • bone marrow failure
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5
Q

what are some causes of macrocytic anaemia?

MCV > 98fL

A
  • haematinic deficiency
  • haemolysis
  • other non-megaloblastic causes
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6
Q

what is leukopenia?

A

Low total WBC count. Can occur because of a reduction in number of all WBCs or specific cells e.g. neutrophils (neutropenia), lymphocytes (lymphopenia).

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7
Q

what is leucocytosis?

A

High total WBC count. Either from increase in all WBCs or specific cells e.g. neutrophils (neutrophilia), eosinophils (eosinophilia), lymphocytes (lymphocytosis).

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8
Q

what is thrombocytopenia?

A

A reduced platelet count.
Caused by decreased production or increased consumption of platelets.

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9
Q

what is thrombocytosis?

A

A high platelet count. Caused by increased production (e.g. response to inflammation) or decreased consumption (hyposplenism).

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10
Q

What is pancytopenia?

A

Combination of:
- anaemia (low red blood cells)
- thrombocytopenia (low platelets)
- leucopenia (low white blood cells)

Happens when abnormal myeloid stem cells in the bone marrow do not develop into normal blood cells.

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11
Q

Pancytopenia symptoms

A

Often vague at first:
- anaemia: tiredness, breathlessness
- more frequent infections: fever, cough, headache
- abnormal bleeding: nose bleeds, bleeding gums, bruising, blood clots.
- bone pain in your back or hips.
- other: weight loss, loss of appetite, swollen glands and headaches.

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12
Q

what are some causes of bone marrow failure?

A
  • malignancy/clonal: blood and others
  • drugs: chemotherapy, other cytotoxics, antibiotics
  • infection (HIV)
  • nutritional
  • radiation, poisons
  • congenital
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13
Q

define acute leukaemia

A
  • A cancer of ‘blast’ cells in bone marrow.
  • Blasts crowd out normal haematopoiesis and cause marrow failure.
  • They circulate in blood and can cause enlarged spleen or liver.
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14
Q

define chronic leukaemia

A
  • Cancers of marrow where lymphocytes (CLL) or granulocytes (CML) spill into blood and infiltrate the liver, spleen (and lymph nodes in CLL).
  • Marrow failure can occur late in disease.
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15
Q

what is a lymphoma?

A
  • A cancer of lymphocytes in lymph nodes and extra-nodal areas (spleen, liver, bone marrow etc).
  • If lymphoma is in the bone marrow you may find lymphoma cells in the blood.
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16
Q

Since Non-Hodgkin’s lymphomas (NHLs) are such a diverse group of diseases, clinicians often subdivide them:

A

Low grade:
- Indolent: grow over months-years.
- may not require treatment until symptoms develop.
- treat to induce remission but not cure.

High grade:
- aggressive
- life-threatening and need urgent treatment
- often more curable

17
Q

Describe the Prothrombin Time test.

A coagulation screen test

A
  • The PT is the time taken for the sample of blood to clot after tissue facter and calcium are added.
  • normal range: 10-13.5 seconds
  • test of: extrinsic (and common) pathways (PeT)
18
Q

what causes a prolonged Prothrombin time?

A
  • problems with factors II, V, VII, X or fibrinogen (either a deficiency or inhibitor)
  • warfarin use/vitamin K deficiency
  • liver disease +++
  • disseminated intravascular coagulation (DIC)
19
Q

Describe a APTT.

a coagulation screen test

A
  • aPTT is the time taken for the sample of blood to clot after a contact activator and Ca2+ are added.
  • normal range: 25-35 seconds
  • test of: intrinsic (and common) pathway (A PinTT)
20
Q

what causes a prolonged aPTT?

A
  • problems with factors II, V, VIII, IX, X, XII or fibrinogen
  • heparin therapy
  • ‘lupus anticoagulant’/antiphosphilipid antibodies
  • liver disease +
  • disseminated intravascular coagulation
22
Q

what are anticoagulant drugs?

A

Anticoagulant drugs interfere with secondary haemostasis (i.e. coagulation factors). We tend to distinguish them from antiplatelet drugs or thrombolytic therapies.

24
Q

how is the severity of haemophilia determines?

25
Q

describe the main functions of plasma

A
  • Transporting blood cells
  • Transporting nutrients and waste: Plasma carries nutrients, hormones, and proteins to the body’s cells, and waste products away from the cells.
  • Maintaining blood pressure and volume
  • Maintaining pH balance
  • Regulating body temperature
  • Clotting blood
  • Supporting immunity
  • Maintaining fluid balance
  • Supporting blood vessels
26
Q

what is the function of the spleen?

A
  • filtering blood: removes old and damaged red blood cells, as well as germs and other abnormal cells.
  • controlling blood cell levels
  • producing immune system components: lymphocytes and antibodies
  • storing blood and iron for body to use later
  • regulating blood flow
27
Q

what are some causes of splenomegaly?

A

- infections: HIV, tuberculosis, endocarditis, malaria, toxoplasmosis.
- liver disease: chronic hepatitis or chirrhosis

- cancer: leukemia, myeloproliferative neoplasms (MPNs) aand lymphomas.
- focal lesions
- autoimmune disease: lupus, sarcoidosis, RA.
- inherited metabolic disorders e.g. sickle cell
- thrombosis