6. Haematology Flashcards

1
Q

Where are the sites of haemopoiesis throughout the life of a foetus?

A

0-2 months - yolk sac
2-5 months - liver and spleen
5-9 months - bone marrow

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2
Q

What are the sites of haemopoiesis in an infant?

A

Bone marrow of most bones.

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3
Q

Which bones have bone marrow as a site for haemopoiesis in an adult?

A

Vertebrae, ribs, sternum, sacrum + pelvis, proximal ends of femur.

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4
Q

What is produced in bone marrow?

A

RBC, platelets, and most WBC.

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5
Q

What is bone marrow?

A

Soft, spongy, gelatinous tissue in the hollow spaces in the interior of bones.

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6
Q

What are the two types of bone marrow?

A

Red marrow and yellow marrow.

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7
Q

What does red marrow mainly contain?

A

Haematopoietic tissue.

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8
Q

What does yellow marrow mainly contain?

A

Fatty tissue.

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9
Q

What are the stages of myeloid precursors?

A

Myeloblast, promyelocyte, myelocyte, metamyelocyte, band cell, neutrophil.

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10
Q

What are the stages of RBC precursors?

A

Proerythroblasts, early normoblast, intermediate normoblast, late normoblast, reticulocyte, RBC.

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11
Q

What do megakaryocytes in the BM produce?

A

Platelets.

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12
Q

What is platelet production controlled by?

A

TPO - thrombopoietin.

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13
Q

What does the spleen contain?

A

Red and white pulp.

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14
Q

What is the red pulp in the spleen?

A

Sinuses lined by endothelial macrophages and cords.

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15
Q

What is the white pulp in the spleen?

A

Similar structure to lymphoid follicles.

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16
Q

What is the main source of blood for the spleen?

A

The splenic artery.

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17
Q

What is the role of the white pulp of the spleen?

A

Screen for infection.

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18
Q

What is the role of the red pulp of the spleen?

A

Sequester RBC that are damaged.

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19
Q

What are the functions of the spleen?

A

Sequestration and phagocytosis, blood pooling, extramedullary haemopoiesis, immunological function.

20
Q

What is extramedullary haemopoiesis?

A

When pluripotent stem cell proliferate during haematological stress or if marrow fails.

21
Q

What can cause splenomegaly?

A

Back pressure (portal hypertension), overworking red or white pulp, extramedullary haemopoiesis, infiltrated by cancer cells or other material.

22
Q

What are the causes of massive splenomegaly?

A

Chronic myeloid leukaemia, myelofibrosis, chronic malaria, Schistosomiasis.

23
Q

What are the causes of moderate splenomegaly?

A

Chronic myeloid leukaemia, myelofibrosis, chronic malaria, Schistosomiasi, lymphoproliferative disorders, myeloproliferative disorders, liver cirrhosis, infections from EBV.

24
Q

What are the causes of mild splenomegaly?

A

Chronic myeloid leukaemia, myelofibrosis, chronic malaria, Schistosomiasi, lymphoproliferative disorders, myeloproliferative disorders, liver cirrhosis, infections from EBV or hepatitis or endocarditis, sarcoidosis, AI diseases.

25
What are the risks of splenomegaly?
Risk of rupture.
26
What is hyposplenism?
Lack of functioning splenic tissue.
27
What are the causes of hyposplenism?
Splenectomy, sickle cell disease, coeliac disease.
28
What do hyposplenic blood film show?
Howell Jolly bodies.
29
What are patients with hyposplenism at risk of?
Overwhelming sepsis, particularly from encapsulated organisms.
30
What is cytopenia?
Reduced number of blood cells.
31
What is anaemia?
Low RBC count.
32
What is leucopenia?
Low WCC.
33
What is neutropenia?
Low neutrophils.
34
What is thrombocytopenia?
Low platelets.
35
What is pancytopenia?
Low RBC, WCC, and platelets.
36
What are the causes of immuno thrombocytopenic purpura?
Autoantibodies against GP IIb/IIIa and GPIb/IX; secondary to autoimmune disease e.g. SLE, lymphoma, CLL.
37
How is ITP treated?
Immunosuppression.
38
What are microangiogpathic haemolytic states?
Pathological activation of coagulation causes numerous microthrombi to form in the circulation -> consumption of clotting factors and platelets and haemolytic anaemia.
39
What can reduce production leading to thrombocytopenia?
B12 or folate deficiency, cancer or fibrosis of bone marrow, aplastic anaemia, drugs, viruses.
40
What are the consequences of severe thrombocytopenia?
Easy bruising, petechiae, purpura, mucosal bleeding, severe bleeding after trauma, intracranial haemorrhage.
41
What can reduce production leading to neutropenia?
B12 or folate deficiency, cancer or fibrosis of the bone marrow, aplastic anaemia, radiation, drugs, virus, congenital disorders.
42
What are the consequences of neutropenia?
Severe life threatening bacterial or fungal infection, mucosal ulceration.
43
What can reduce production leading to pancytopenia?
B12 or folate deficiency, cancer or fibrosis of the bone marrow, idiopathic immune aplastic anaemia, radiation, drugs, virus, congenital disorders.
44
What is aplastic anaemia?
Pancytopenia with hypocellular bone marrow in the absence of an abnormal infiltrate with no increase in reticulin.
45
What are the malignancies causing pancytopenia?
Haematological - acute and chronic leukaemia, lymphoma, myeloma, myelofibrosis, myelodysplastic syndrome; non-haematological malignancy - prostate, breast, lung.
46
What are the symptoms of pancytopenia? (Break it down into anaemia, thrombocytopenia, neutropenia).
Anaemia - fatigue, dizziness, chest pain, shortness of breath. Thrombocytopenia - bleeding, bruising etc. Neutropenia - infection, ulcers, fevers.