Interactive Leukaemia Cases Flashcards

1
Q

Indian, 5M presented with lymphadenopathy + mediastinal mass on CXR
WBC: 180
Hb: 93
Platelets: 43
Describe these results

A

WBC: V high (exceeds infection)
Hb: Low
Platelets: Low

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2
Q

Indian, 5M presented with lymphadenopathy + mediastinal mass on CXR
WBC: 180
Hb: 93
Platelets: 43
What is seen on the blood film?

A

Anaemia: blood less viscous, less Hb
Severe thrombocytopenia: No platelets
Abnormal large light purple cells: blasts

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3
Q

Indian, 5M presented with lymphadenopathy + mediastinal mass on CXR
WBC: 180
Hb: 93
Platelets: 43

What is the most likely cause of the mediastinal mass? Why?
A. Thymoma
B. AML
C. ALL
D. Haemorrhage into mediastinum
E. Pneumonia with a leukaemoid reaction

A

C. ALL

V high WBC in a child strongly indicative of leukaemia

Low Hb + Platelets result from BM infiltration

Mediastinal mass is the Thymus infiltrated by T lymphoblasts

(Thymoma unlikely due to high WCC)

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4
Q

Indian, 5M presented with lymphadenopathy + mediastinal mass on CXR
WBC: 180
Hb: 93
Platelets: 43
What would be the best technique to confirm the diagnosis of ALL? What approach to management should be taken?
A. Immunophenotyping
B. Cytochemistry

A

A. Immunophenotyping

For lymphoblasts cytochemistry does not predict anything

Combination chemotherapy + CNS directed therapy

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5
Q

48M railway engineer.
2/52 bleeding gums
Attended dentist- severe bleeding
1 episode haematuria

Left subconjunctival haemorrhage
Small bruises over abdo
No enlarged LN
No hepatosplenomegaly

What test is most likely to reveal the cause of the problem?
A. Liver function tests
B. Creatinine
C. Coagulation screen
D. Blood count, film and coagulation screen

A

D. Blood count, film + coagulation screen

Blood film can confirm Thrombocytopenia
(exclude pseudothrombocytopenia from clumping)

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6
Q

48M railway engineer.
2/52 bleeding gums
Attended dentist- severe bleeding
1 episode haematuria
LFTs:
ALT: 97
ALP: 72
BR: 24
Interpret these LFTs

A

ALT: HIGH
ALP: Normal
BR: HIGH

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7
Q

48M railway engineer.
2/52 bleeding gums
Attended dentist- severe bleeding
1 episode haematuria

WBC: 7.5
Hb: 109
MCV: 83
Platelets: 21

Interpret this FBC

A

WBC: Normal
Hb: Low
MCV: Normal- Low
Platelets: Low

Borderline anaemia + severe thrombocytopenia

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8
Q

48M railway engineer.
2/52 bleeding gums
Attended dentist- severe bleeding
1 episode haematuria

PT: 13.4 s
APTT: 21.5 s
Fibrinogen: 0.97 g/l

Interpret this coagulation screen

How could you explain a short APTT and a low fibrinogen?
What other test do you need?

A

PT: Normal
APTT: Low
Fibrinogen: Low

Consumption of fibrinogen + short APTT raises suspicion of DIC: activated coagulation factors in circulation making APTT short

Blood film +/- D-dimer

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9
Q

48M railway engineer.
2/52 bleeding gums
Attended dentist- severe bleeding
1 episode haematuria

Short APTT, low fibrinogen

What cells can be seen on his blood film? How could you prove it?

A

Myeloid
Contain Auer rods + Granules

Prove difference between lymphoid + myeloid with cytochemistry or immunophenotyping

(but neither is actually necessary)

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10
Q

48M railway engineer.
2/52 bleeding gums
Attended dentist- severe bleeding
1 episode haematuria

What can be seen on the bone marrow biopsy?

A

Granular blast cells replacing healthy BM cells
Uniform population- abnormal in the same way

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11
Q

48M railway engineer.
2/52 bleeding gums
Attended dentist- severe bleeding
1 episode haematuria

Borderline anaemia, severe thrombocytopenia

Short APTT, low fibrinogen

Uniform, granular blast cells on BM biopsy

What diagnosis do you suspect?
A. CML
B. Acute promyelocytic leukaemia
C. Some other type of acute myeloid leukaemia
D. ALL

A

B. Acute promyelocytic leukaemia

Uniform population of promyelocytes with Auer rods + granules
Features of DIC

If CML would have myeloid hyperplasia in BM with differentiation into eosinophils, basophils + neutrophils

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12
Q

48M railway engineer.
2/52 bleeding gums
Attended dentist- severe bleeding
1 episode haematuria

Which test would be most useful to confirm the diagnosis of acute promyelocytic leukaemia?
A. Cytochemistry
B. Immunophenotyping
C. Cytogenetic analysis/ FISH/ molecular genetic analysis

What would you expect to see?

A

C. Cytogenetic analysis
Show t(15;17)
forming PML-RARA fusion gene (seen on FISH)

Want to determine APML from AML

Not immunophenotyping: already know this is myeloid- Auer rods

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13
Q

What is immunophenotyping good for in leukaemia?

A

Determine LYMPHOID from MYELOID
Will show antigens

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14
Q

What is cytogenetic analysis/ FISH/ molecular genetic analysis good for in leukaemia?

A

Identifying MUTATIONS

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15
Q

68F presenting with gradual onset fatigue, lethargy and exertion dyspnoea
Non smoker, not much alcohol, good diet
Pallor: conjunctival and nail bed
Mild ankle oedema

What one test would you do next?

A

FBC

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16
Q

68F presenting with gradual onset fatigue, lethargy and exertion dyspnoea
Non smoker, not much alcohol, good diet
Pallor: conjunctival and nail bed
Mild ankle oedema

Macrocytic anaemia on FBC
MCV: 110

Which test should be done next?
A. Blood film
B. BMA
C. LFTs
D. Thyroid function tests
E. Serum vitamin B12 and red cell folate

A

A. Blood film
Quick + simple

17
Q

68F presenting with gradual onset fatigue, lethargy and exertion dyspnoea
Non smoker, not much alcohol, good diet
Pallor: conjunctival and nail bed
Mild ankle oedema

Her blood film looked like this. Describe the blood film.

A

Macrocytes + Microcytes (dimorphic)
Hypochromic microcytes
Neutrophils look normal
No oval macrocytes/ no hyper-segmentation to suggest B12 or folate deficiency

18
Q

68F presenting with gradual onset fatigue, lethargy and exertion dyspnoea
Non smoker, not much alcohol, good diet
Pallor: conjunctival and nail bed
Mild ankle oedema

serum B12, red cell folate, LFTs, TFTs = normal
Ferritin 875 (grossly elevated)
BMA: 12% blast cells, 45% of erythroblasts were ring sideroblasts

What is the diagnosis?

A

Myelodysplastic syndrome (MDS with excess of blasts)

Dimorphic blood films suggestive of acquired sideroblastic anaemia: macrocytosis + subpopulation of hypo chromic microcytes

BMA: normal blast cells <5%

Ringed sideroblasts- ring of haemodesrin around nucleus on blood film (top arrow)
Abnormal sideroblasts- not ringed, random assortment (bottom arrow)

19
Q

Indian 72F
Vegetarian, teetotal, non smoker
SOBOE, fatigue, painful gums and tongue, unable to eat spicy food
Pallor
WBC normal
Hb 52
MCV 122
Platelet count normal
Describe her blood film.
What should be measured next?

A

Oval macrocytes
Hypersegmented neutrophil
Tear drop poikilocytes
Severe anaemia

Vitamin B12 and folate as classic film of pernicious/ other megaloblastic anaemia

20
Q

Indian 72F
Vegetarian, teetotal, non smoker
SOBOE, fatigue, painful gums and tongue, unable to eat spicy food
Pallor

B12, folate, TFT normal
LFTs mildly impaired
LDH 3870

What would you do next? Why?

A

Bone marrow aspirate as potentially a high cell turnover

21
Q

Indian 72F
Vegetarian, teetotal, non smoker
SOBOE, fatigue, painful gums and tongue, unable to eat spicy food
Pallor

What can be seen on this bone marrow aspirate? Do you think this patient has a myelodysplastic syndrome?

A

LHS: Giant metamyelocytes
RHS: Megaloblasts

Not MDS

22
Q

Indian 72F
Vegetarian, teetotal, non smoker
SOBOE, fatigue, painful gums and tongue, unable to eat spicy food
Pallor

Parietal cell antibodies: +ve
Intrinsic factor antibodies: +ve
Schilling test: 0% excretion

Interpret these results

A

+ve parietal cell + intrinsic factor antibodies suggest Pernicious anaemia

Schilling test: proves can’t absorb bit B12

(had normal B12 assay- sometime defective assays when IF antibodies in serum)

23
Q

70F referred to vascular surgeon due to gangrenous toes
Non diabetic, 50-pack-year-hx
SOBOE and morning cough
Reduced femoral and distal pulses on side of affected toes
Not SOB at rest, no cyanosis
Plethora, conjunctival suffusion
No spleen felt

WBC: 18.6
Hb: 180
Platelets: 1648

USAP: normal kidneys, increased splenic size

What is the most likely diagnosis?
A. CML
B. Essential thrombocytopenia
C. Polycythemia vera
D. COPD

A

C. Polycythaemia vera

In ET would NOT get high Hb
In COPD would NOT get high platelets
In CML would NOT get high Hb

24
Q

70F referred to vascular surgeon due to gangrenous toes
Non diabetic, 50-pack-year-hx
SOBOE and morning cough
Reduced femoral and distal pulses on side of affected toes
Not SOB at rest, no cyanosis
Plethora, conjunctival suffusion
No spleen felt

WBC: 18.6
Hb: 180
Platelets: 1648

USAP: normal kidneys, increased splenic size

What test would you do to confirm diagnosis of polycythaemia vera?
A. Molecular analysis for JAK2 mutation
B. Measure total volume of red cells in circulation
C. BMA and trephine biopsy

A

A. Molecular analysis for JAK2 mutation

25
Q

70F referred to vascular surgeon due to gangrenous toes
Non diabetic, 50-pack-year-hx
SOBOE and morning cough
Reduced femoral and distal pulses on side of affected toes
Not SOB at rest, no cyanosis
Plethora, conjunctival suffusion
No spleen felt

WBC: 18.6
Hb: 180
Platelets: 1648

USAP: normal kidneys, increased splenic size

How would you treat this patient with polycythaemia vera?
A. Venesection alone
B. Imatinib
C. Venesection plus hydroxycarbamide
D. 32P

A

C. Venesection plus hydroxycarbamide

Venesection reduces Hb quite fast + depletes iron stores to prevent rapid rise again
Hydroxycarbamide to reduce platelets

26
Q

70F referred to vascular surgeon due to gangrenous toes
Non diabetic, 50-pack-year-hx
SOBOE and morning cough
Reduced femoral and distal pulses on side of affected toes
Not SOB at rest, no cyanosis
Plethora, conjunctival suffusion
No spleen felt

WBC: 18.6
Hb: 180
Platelets: 1648

USAP: normal kidneys, increased splenic size

Why is venesection alone unsuitable treatment for this patient?

A

Venesection alone will not address the high platelet count, thus need hydroxycarbamide