Haematology Scott Notes Flashcards

1
Q

Causes of MAHA

A

DIC HUS TTP

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2
Q

B thalassemias are caused by what mutations?

A

Point

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3
Q

A thalassemias are caused by what mutations ?

A

Deletions

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4
Q

Hb in Thalassemia trait

A

HbA2

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5
Q

Target cells

A

HbC disease
Asplenemia
Liver disease
Thalassemia

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6
Q

What to ask someone with anaemia on an OSCE

A

Vegan/vegetarian diet

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7
Q

Symptoms of subacute degeneration of the cord

A

Dorsal column and corticospinal tracts
Also spinocerebellar

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8
Q

Pernicious anaemia increases your risk for

A

Gastric adenocarcinoma

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9
Q

Pernicious anaemia more common in what blood group?

A

A

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10
Q

Schistocytes

A

MAHA and mechanical heart valve

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11
Q

TTP caused by

A

Genetic or acquired deficiency of ADAMTS13

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12
Q

DAT + haemolytic anaemia
DAT - haemolytic anaemia

A

MAHA, AIHA
Hereditary spherocytosis

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13
Q

What is the defect in G6PD deficiency ?

A

X-linked disorder of pentose phosphate shunt
Decreased NADPH production –> RBC oxidative damage

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14
Q

Triggers of haemolysis in G6PD deficiency

A

Fava beans
Sulpha drugs
Infection
Dapsone
Antimalarials

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15
Q

Test for G6PD

A

Have to do after 8 weeks again

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16
Q

Sickle cell anaemia

A

HbSS

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17
Q

Sickle cell trait

A

HbAS

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18
Q

Defect in SS

A

Glutamic acid -> valine

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19
Q

Aplastic crisis caused by

A

Parovrisu B19

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20
Q

Treat acute crisis in sickle cell

A

Analgesia (opioids)
Hydrate
O2

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21
Q

Intrinsic pathway

A

8,9,11,12

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22
Q

Extrinsic pathway

A

7

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23
Q

What to ask someone in OSCE if they are anaemic?

A

Blood loss, do they tend to bleed after surgery

24
Q

Avoid what drugs in Haemophilia

A

NSAIDS

25
Q

Treat Haemophilia

A

Desmopressin and tranexamic acid

26
Q

What cancer can cause DIC?

A

APML

27
Q

Protein C deactivates

A

Factor 5 and 8

28
Q

AT is a cofactor for

A

Heparin

29
Q

What can cause acquired thrombophilia

A

Progesterone in OCP

30
Q

Excess RBC

A

Polycythemia vera

31
Q

Excess WBC

A

CML

32
Q

Excess platelets

A

ET

33
Q

Excess megakaryocytic

A

Myelofibrosis

34
Q

CMD have

A

Hypercellular bone marrow

35
Q

EPO in PV

A

Decreased

36
Q

Acute leukemia on blood film

A

Blasts >20%

37
Q

CML Ix diagnostic

A

Auer rods

38
Q

CLL blood levels

A

Increased WCC
Decreased RBC, PMN Plats

39
Q

Richter transformation

A

CLL-> large B cell lymphoma

40
Q

Philadelphia chromosome

A

9:22
CML

41
Q

Treat CML?

A

Imatinib

42
Q

Hodgkin’s lymphoma age

A

20-29 and >60

43
Q

Increased LDH

A

Non-hodgkins

44
Q

B cell classification of non-hodgkins

A

Low: follicular, marginal, waldenstrom’s
High: diffuse large B cell, burkitt’s

45
Q

Adult T cell lymphoma

A

HTLV-1

46
Q

Plasma cells Ig in multiple myeloma

A

IgG IgA

47
Q

Increased in what IL in MM

A

IL-6 which inhibits osteoblasts

48
Q

Bloods in MM

A

ESR increase and normal ALP

49
Q

Over 50 and backpain do

A

ESR and electrophoresis

50
Q

What biopsy for MM?

A

Trephine BM biopsy

51
Q

Causes of massive splenomegaly

A

CML, myelofibrosis, malaria, leishmaniasis, gaucher’s

52
Q

Hyposplenism on film

A

Howell-Jolly
Pappenheimer
Target

53
Q

What creates the rouleaux?

A

Increased ESR

54
Q

Pencil cells

A

IDA

55
Q

Spherocytes

A

AIHA
Hereditary spherocytosis