MRCP Haematology Flashcards

1
Q

Microcytic anaemia, raised HbA2 (>3.5%)

A

Beta thalassaemia trait

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2
Q

Two main complications of polycythaemia vera

A

Thrombosis and bleeding

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3
Q

Bleeding prophylaxis in patient with vWD

A

DDAVP (desmopressin) and tranexamic acid

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4
Q

Two commonest causes of gross splenomegaly

A

CML, myelofibrosis

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5
Q

Blood film seen in myelofibrosis

A

Leucoerythroblastic cells, tear drop cells

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6
Q

Anaemia & marrow biopsy showing fatty bone marrow

A

Aplastic anaemia

AI attack against haematopoietic stem cells

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7
Q

Intensity and duration of anticoagulation in antiphospholipid syndrome?

A

INR 2-3, lifelong

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8
Q

What vitamin helps with the absorption of oral iron?

A

Vitamin C

Reduces iron from ferric to ferrous form

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9
Q

Empirical treatment of neutropaenic sepsis

A

Tazocin (piperacillin & tazobactam)

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10
Q

Red cells showing osmotic fragility

A

Hereditary spherocytosis

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11
Q

Underlying cause of haemolysis in G6PD deficiency

A

Reduced levels of NADPH

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12
Q

APTT & PT in anti-phospholipid syndrome

A

APTT prolonged

PT NORMAL

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13
Q

Tissue sampling required to make diagnosis of lymphoma

A

Lymph node extraction & biopsy.

FNA not adequate!

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14
Q

Tests for determining prognosis in myeloma

A

Albumin and B2-microglobulin

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15
Q

What surface receptor is the target for immunotherapy in lymphoma?

A

CD20

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16
Q

Best test to confirm invasive aspergillosis

A

Galactomannan

17
Q

Translocation in acute promyelocytic leukaemia

18
Q

Anaemia + gallstones = ?genetic condition

A

Hereditary spherocytosis

19
Q

Bleeding prophylaxis in vWD pre dental procedure

A

Desmopressin

20
Q

Treatment of APML (often presents with DIC)

A

All-trans-retinoic acid (vitamin A derivative)

21
Q

Infection prophylaxis for people taking fludarabine

A

Co-trimoxazole

fludarabine is treatment for CLL

22
Q

Pathophysiology behind warfarin induced skin necrosis

A

Protein C deficiency (it is vit K dependent and rapidly falls on commencing warfarin leading to paradoxical prothrombotic state)

23
Q

Peripheral blood film blast cells, gum hypertrophy, splenomegaly

A

AML (Auer rods also)

24
Q

Lymphadenopathy, anaemia, smudge/smear cells on blood film. What investigation? Whats the diagnosis?

A

Diagnosis: CLL
Investigation: Immunophenotyping

25
Acute treatment of hyperviscosity syndrome
Plasmapheresis
26
Bone marrow aspiration showing lymphoplasmacytoid cells
Waldestrom's macroglobulinaemia
27
Dry bone marrow aspirate, bone marrow biopsy - fried egg appearance, TRAP stain positive
Hairy cell leukaemia
28
Bone marrow stain positive for Sudan black, myeloperoxidase and non-specific esterase ++
Acute monocytic leukaemia (type of AML)
29
Ligamentous laxity, thromboembolic events and short-sightedness suggest which diagnosis?
Homocystinuria
30
First line treatment for ITP?
HIGH dose steroids
31
Treatment for HELLP syndrome
Delivery of baby/placenta
32
Only clotting factor unique to PT
Factor VII
33
Leucocytes expressing CD5 when stained (immunophenotyping)
CLL
34
Absent CD55 and CD59 on red cell surface
Paroxysmal noctural haemoglobinuria (PNH)
35
Haemophilia B is associated with which clotting factor deficiency?
Factor IX (9)
36
Translocation t(15;17)
Acute promyelocytic leukaemia
37
Pancytopenia and bone marrow biopsy showing increased cellularity
Myelodysplasia
38
Translocation of chromosomes 9 and 22
Philadelphia chromosome | CML