Haematology Flashcards

1
Q

4 symptoms of lymphoma

A

rubbery lump in neck
fever
night sweats
weight loss
painful nodes when drinking alcohol
pruritis

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2
Q

Name 2 signs you will look for on examination in lymphoma

A

Enlarged lymph nodes
Splenomegaly
Hepatomegaly

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3
Q

Classical cell name that suggests Hodgkin’s lymphoma

A

Reed-sternberg cell

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4
Q

State 2 staging investigations for Hodgkins

A
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5
Q

What staging system is used for Hodgkins?

A

Lugano classification

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6
Q

Hodgkins pt with dyspnoea, swelling of face and congested veins in neck and chest - what has happened

A

SVCO

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7
Q

Name 3 signs of anaemia

A

Tachypnoea
Pale conjunctiva
Tachycardia
Ejection systolic murmur

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8
Q

Other than menorrhagia, name one other cause of iron-deficiency anaemia

A

Inadequate dietary intake
Internal bleeding e.g. malignancy

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9
Q

Name 2 specific signs of chronic iron-deficiency anaemia

A

Angular cheilosis
Koilionychia
Atrophic glossitis

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10
Q

Name 2 common side effects of ferrous sulphate

A

Dark sticky stools
Nausea
Constipation
Diarrhoea

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11
Q

Name 2 drugs used in the long term treatment of sickle cell anaemia

A

Hydroxycarbomide
Penicillin V

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12
Q

Other than infection, name 2 factors that can bring on a sickle-cell crisis

A

Dehydration
Exposure to cold
Hypoxia
Acidosis

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13
Q

State 3 general points in managing a vaso-occlusive sickle cell crisis

A

Oxygen
Analgesia
IV fluids
Empirical abx

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14
Q

Pattern of inheritence of sickle-cell disease?

Likelihood of children carrying sickle cell if partner has normal chromosomes?

A

Autosomal recessive

100%

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15
Q

Why does sickle cell not clinically manifest until roughly 6 months of age

A

Fetal Hb mask the effect of the disease

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16
Q

What is multiple myeloma

A

Malignant clonal proliferation of B-lymphoacytic plasma cell

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17
Q

What is the commonest immunoglobulin expressed as part of multiple myeloma

A

IgG

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18
Q

Other than bone pain, name 2 other symptoms of multiple myeloma

A

Recurrent infections
Bruise easily
Tiredness
Polydipsia
Abdominal pain
Confusion

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19
Q

Except an X-ray, name 3 investigations you would perform for multiple myeloma

A

FBC
Blood film
U&E
Serum electrophoresis
Urine electrophoresis
Serum calcium
Serum immunoglobulins
Bone marrow sampling

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20
Q

Why are multiple myeloma patients prone to infections

A

Bone marrow infiltration (low WCC)
Immunoparesis secondary to overexpression of one immunoglobulin

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21
Q

State 4 complications of myeloma

A

Hypercalcaemia
Spinal cord compression
Hyperviscosity
Acute renal failure

22
Q

Name 2 causes for splenomegaly other than leukaemia

A

Haemolytic anaemia
Malaria
Lymphoma
Liver cirrhosis w/ portal hypertension

23
Q

Chronic leukaemia WCC?

24
Q

How could you differentiate on a blood film between acute leukaemia and chronic leukaemia?

A

AL: immature WBC
CL: mature WBC

25
Q

What leukaemia has the characteristic philadelphia chromosome?

26
Q

Bone marrow aspirate with 95% cancer cells after medical treatment - management?

A

Bone marrow transplant

27
Q

3 FBC findings in bone marrow failure

A

Thrombocytopenia
Anaemia
Leucopenia/neutropenia

28
Q

Why do you get bone pain in bone marrow failure

A

Marrow infiltration

29
Q

Immediate investigation in possible haematological malignancy

A

Blood film

30
Q

Bone marrow biopsy shows dominant presence of blast cells of myeloid lineage - diagnosis

31
Q

Supportive treatment during stem cell transplantation

A

Blood transfusions (anaemia)
Platelet transfusions (thrombocytopenia)
Prophylactic abx

32
Q

Below what value of Hb should a blood transfusion take place, regardless of symptoms

33
Q

Name 2 signs of severe anaemia

A

Tachycardia
Tachypnoea
Flow murmur
Pallor

34
Q

Fever and hypotension after blood transfusion - differential diagnoses of type of transfusion reaction

A

Acute haemolytic
Bacterial contamination

35
Q

First management step in adverse transfusion reaction

A

stop the transfusion

36
Q

Oozing from cannula site after transfusion reaction - what haematological state has occurred?

37
Q

Other than acute haemolytic, name 1 type of early (24h) transfusion complication and 1 late (after 24h)

A

Allergic
TRALI
TACO

Iron overload
Graft v host
Infection

38
Q

What is the definition of a massive blood transfusion

A

Entire pts blood volume / 10 units within 24h

39
Q

Name 2 causes of each category of macrocytic anaemia

A

Megaloblastic - folate and B12
Normoblastic - thyroid, liver, alcohol

40
Q

What test distinguishes between the 2 categories of macrocytic anaemia

A

blood film

41
Q

Pt w/ addisons disease and vitiligo has macrocytic anaemia - likely cause?

Name a test that could help confirm your diagnosis

A

Pernicious anaemia

Intrinsic factor antibody serology

42
Q

How will you treat the macrocytic anaemia

A

IM hydroxycobalamin

43
Q

Signs of thalassaemia major on examination (2)

A

Hepatosplenomegaly
Frontal bossing
Jaw enlargement
Dental malocclusion
Flow murmur
Generalised pallor

44
Q

Common name given to beta-thalassaemia major

A

Cooley’s anaemia

45
Q

2 main treatments for beta-thalassaemia major

A

Blood transfusion
Iron chelation therapy

46
Q

Why does thalassaemia major never usually present in the first 6 months of life

47
Q

How can haemophilia lead to compartment syndrome and joint deformities

A

Bleeding into joints

48
Q

How is haemophilia A inherited

A

X-linked recessive

49
Q

Which clotting factor is deficient in haemophilia A

50
Q

INR and APTT in haemophilia A

A

normal INR, prolonged APTT

51
Q

Name a treatment for haemophilia A to improve clotting factor deficiency

A

Purified factor 8
FFP containing factor 8
Desmopressin

52
Q

How would you account for a lady being diagnosed with haemophilia A at the age of 70

A

acquired haemophilia A