Interactive case hx in haematology Flashcards

(47 cards)

1
Q

Which of the following is the most convincing indication of iron deficiency? Please rank:

Anaemia and low MCV
Jaundice
Pencil cells on the blood film
Low transferrin saturation plus low serum iron
Fatigue

A

?

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2
Q

Give 2 symptoms and 2 signs of anaemia

A

weakness/ lethargy
Breathlessness

Pallor
Tachycardia + cardiomegaly

extra signs: koilynychia, glossitis, jaundice

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3
Q

Scenario A&E
Age 36
Sex Female
History 2years SOBOE
FBC Hb 32 g/l (116-150g/dl)
WBC 7 x 109/l (2-10.5 x 109/l)
platelets 452 x 109/l (150-400 x 109/l)
MCV 54fl ( 80-100fl)

What are the 3 most likely causes of this anaemia ?

A

Iron Deficiency Anaemia
Thalassaemia
ACD

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4
Q

What further investigations would be useful?

A

Reticulocyte count
- Haemoglobin electrophoresis
Iron studies..e.g. ferritin, transferrin saturation
Blood film

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5
Q

When is reticulocytosis absent?

A

Inadequate haematinics

Bone marrow failure (e.g. infiltration)

Acute major haemorrhage…reticulocyte response within 6 hours which increases over 6-10 days

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6
Q

What is on a blood film in IDA?

A

Iron deficiency

  1. Pencil cells
  2. Anisocytosis
  3. Poilkilocytosis
  4. Hypochromic
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7
Q

What does this show?

A
  1. Pencil cells
  2. Anisocytosis
  3. Poilkilocytosis
  4. Hypochromic
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8
Q

What causes IDA?

A

Uterine blood loss

GI loss

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9
Q

Hb 60 g/l (135-175g/l)

WBC 0.1 x 109/l (2-10.5 x 109/l)

Platelets 4 x 109/l (150-400 x 109/l)

What is abnormal about this blood count?

A
  1. Hb is LOW
  2. WBC is LOW
  3. Platelets LOW
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10
Q

What could cause this combination of abnormalities?

GIVE THREE POSSIBILITIES

A
  1. Aplastic anaemia
  2. Leukemia
  3. Infiltration e.g.Lymphoma, carcinoma
  4. Drugs e.g. chemotherapy
  5. B12/folate deficiency
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11
Q

Give 2 useful further investigations

A
  1. Blood film
  2. Vitamin B12
  3. Folic acid
  4. bone marrow
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12
Q

Suggest one diagnosis

A

ACUTE MYELOID LEUKAEMIA

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13
Q

What are the likely clinical problems going to be?

A

AML

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14
Q

What are the principles of managing this condition?

A

Supportive

  1. Red cell transfusions
  2. Platelet transfusions
  3. Nurse in isolation; prompt antibiotics

Disease related management

Consider chemotherapy

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15
Q

Hb 120g/l (135-175g/l)

WBC 10 x 109/l (2-10.5 x 109/l)

Platelets 28 x 109/l (150-400 x 109/l)

What is abnormal about this blood count?

A

Anemia

Thrombocytopenia

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16
Q

What are the causes of the MAIN abnormality on this FBC ?

A

NOT MAKING PLATELETS

  • drugs e.g. chemotherapy, thiazides,
  • bone marrow disorders e.g. leukemia, aplastic, myelodysplasia, myeloma, infiltration with carcinoma

PREMATURE DESTRUCTION OF PLTS

  • ITP (auto-immune)
  • Disseminated intravascular coagulation
  • heparin
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17
Q

What further investigations could you do? GIVE 3 POSSIBILITIES

A
  1. Coagulation screen
  2. Blood film
  3. Bone marrow aspirate/trephine
  4. ANA/RAPA
  5. HIV
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18
Q

COAGULATION SCREEN

  • APTT 54 seconds (control 40s)
  • INR 2.1

What is abnormal about this coagulation screen?

A
  • Prolonged APTT
  • INR increased
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19
Q

What further investigations would be useful now?

A
  1. Blood film
  2. D-dimers/FDPs
  3. fibrinogen
  4. Blood cultures/CSR/MSU (Septic screen)
  5. Liver function tests
20
Q

What is the diagnosis?

A

Disseminated intravascular coagulation

21
Q

What is the management of DIC?

A

LIAISE WITH HAEMATOLOGY TEAM AND THE HAEM LAB

  • Antibiotics
  • Blood products….Red cells, platelets, cryoprecipitate, FFP
  • Regular blood tests to assess response to products
22
Q

What can alter myeloblasts?

A

<5% in BM is normal

5-10% is myelodysplasia

>20% is AML

If in peripheral blood, may be AML or leukoerythroblastic anaemia

Auer Rods

23
Q

What can alter lymphoblasts?

A

<5% is normal in BM

>20% = ALL

TdT positive (NO AUER RODS)

24
Q

What are the B cell markers?

25
What are the T cell markers?
CD3 CD4 CD8 CD5
26
What are the lymphocyte makrers of maturity?
TdT = immature T/B lymphoblasts Surface Ig = mature B/ plasma cells
27
Hereditary spherocytosis
28
Spherocytes: Auto Immune or Inherited. One test to confirm acquired ? Hb elctrophoresis DAT (direct antiglobulin) Sickle solubility Unconjugated hyperbilirubinaemia
DAT (direct antiglobulin)
29
What is the difference between inherited and acquired haemolytic anaemias?
Inherited = inherited defect of cell Acquired = environment causes damage
30
MAHA Malaria Snake bites Aortic stenosis
31
Woman with SLE and menorrhagia
ACD
32
Why does ACD happen?
33
What causes isolated single lineage cytpaenia with otherwise normal FBC?
34
B12 deficiency
35
Leukoerythroblastic anaemia- Metastatic prostate cancer
36
What causes pancytopaenia?
37
Single most useful haematological test DAT Immunophenotyping for CD19/CD5/CD3 expression HTLV1 serology BCR ABL1 RT-PCR assay JAK2V617F mutation analysis Factor V Leiden screen
BCR ABL1 RT-PCR assay
38
What is the clinical picture of someone with CML?
39
How do leukaemia markers correlate with levels of residual leukaemia in the body?
40
Tyrosine Kinase Inhibitor- Imatinib/ dasatinib
41
Blast crisis
42
JAK2V617F mutation analysis
43
Immunophenotyping for CD19/CD5/CD3 expression (for CLL)
44
What is CLL?
45
Ibrutinib
46
Multiple Myeloma
47
Cast Nephropathy