Haematology Flashcards

(80 cards)

1
Q

Hypercalcemic crisis

A

Multiple myeloma

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2
Q

Microcytic anaemia with normal RDW?

A

Beta-thalassemia

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3
Q

Microcytic anaemia with high RDW?

A

Iron deficiency anaemia

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4
Q

Blood film for thalassemia?

A

Heinz bodies (alpha)
Basophilic stippling
Target cells

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5
Q

What condition has tear-drop poikilocytes?

A

Myelofibrosis

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6
Q

Presentation of hereditary spherocytosis?

A
Failure to thrive
Jaundice, gall stones
Splenomegaly
Aplastic crisis precipitated by parvovirus infection
CHC elevated
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7
Q

Hereditary spherocytosis?

A
Autosomal dominant
Extravascular haemolysis
Neonatal jaundice
Gallstones
Northern European
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8
Q

G6PD deficiency?

A

X linked recessive
African-Mediterranean
Intravascular haemolysis

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9
Q

Blood film of G6PD?

A

Heinz bodies

Increased reticulocytes

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10
Q

Blood film of hereditary spherocytosis?

A

Spherocytes - round, lack of central pallor

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11
Q

How to diagnose hereditary spherocytosis?

A

Abnormal blood film + family history + raised MCHC

EMA binding test

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12
Q

How to diagnose G6PD?

A

Measure enzyme activity

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13
Q

Causes of massive splenomegaly?

A
Myelofibrosis
Chronic myeloid leukaemia
Visceral leishmaniasis
Malaria
Gaucher's syndrome
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14
Q

What is gaucher’s syndrome?

A
Accumulation of glucocerebroside in cells and organs
Fatigue
Anaemia
Low platelet
Hepatosplenomegaly
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15
Q

Haemophilia A?

A

X linked recessive

Factor VIII deficiency

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16
Q

Haemophilia B?

A

X linked recessive

Factor IX deficiency

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17
Q

Features of haemophilia?

A

Prolonged APTT
Normal thrombin time
Normal prothrombin time

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18
Q

Blood film for CLL?

A

Smudge/smear cells

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19
Q

Blood film for AML?

A

Auer rods

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20
Q

What is chronic lymphocytic leukaemia?

A

Monoclonal proliferation of well differentiated lymphocytes, almost always B cells

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21
Q

Features of CLL?

A
Often none
Anorexia
Weight loss
Bleeding
Infection
Lymphadenopathy
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22
Q

Complication of CLL?

A

Anaemia
Hypogammaglobulinemia
Warm autoimmune haemolytic anaemia
Transformation to high grade lymphoma

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23
Q

What is Richter’s transformation?

A

CLL to high grade lymphoma

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24
Q

Normocytic anaemia?

A
Anaemia of chronic disease
Chronic kidney disease
Aplastic anaemia
Haemolytic anaemia
Acute blood loss
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25
What is thrombocytosis?
High platelet count >400
26
Causes of thrombocytosis?
Reactive Malignancy Essential thrombocytosis Hyposplenism
27
What is essential thrombocytosis?
``` Myeloproliferative disorders Overlaps with CML, polycythemia rubra vera and myelofibrosis >600 platelet count Thrombosis or haemorrhage JAK2 mutation common 'Burning hands' ```
28
Target cells?
``` Sickle cell Thalassemia Iron deficiency Hyposplenism Liver disease ```
29
Blood film for hypospleniam?
``` Target cells Acanthocytes Howell-jolly bodies Siderotic granules Pappenheimer bodies ```
30
What are schistocytes?
Helmet cells | Intravascular haemolysis
31
Blood film of megaloblastic anaemia?
Hypersegmented neutrophils
32
Blood film of iron deficiency anaemia?
Target cells | Pencil poikilocytes
33
What is immune thrombocytopenia?
Antibodies against glycoprotein IIb/IIIa or Ib-V-IX complex
34
Chronic myeloid leukemia
Philadelphia chromosome BCR-ABL T(9.22) Decreased leukocyte alkaline phosphatase
35
Features of lead poisoning?
``` Abdominal pain Peripheral neuropathy Fatigue Constipation Blue lines on gum margin ```
36
Blood film for lead poisoning?
Basophilic stippling | Clover leaf morphology
37
Causes of leukopenia?
``` Steroid therapy SLE AIDS Uremia Chemo ```
38
Causes of eosinophilia?
``` Asthma Eczema Hypersensitivity Rheumatoid Churg-strauss Infection Neoplasia Addision's ```
39
Raised platelets?
Thrombocytosis
40
Low platelets?
``` Thrombocytopenia <150 Reduced production Reduced survival Dilution of numbers ```
41
Causes of microcytic anaemia?
Iron deficiency anaemia Sideroblastic anaemia Thalassemia
42
What is sideroblastic anaemia?
Inadequate use of iron to make haemoglobin | Ringed appearance due to iron deposition in RBC
43
Causes of normocytic anaemia?
``` Haemolytic anaemia Aplastic anaemia Anaemia of renal disease Anaemia of chronic disease Parvovirus Leukemias ```
44
How to differentiate between normocytic anaemias?
Reticulocyte count Raised = haemolytic anaemia Normal/low = other cause
45
Causes of macrocytic anaemia?
``` Chronic liver disease Alcoholism Vitamin B12 deficiency Folate deficiency Myelodysplasia ```
46
Differentiation between macrocytic anaemias?
Megaloblasts on smear
47
Megaloblastic macrocytic anaemia?
Vitamin B12 or folate deficiency
48
Non-megaloblastic macrocytic anaemia?
Alcohol abuse Myelodysplastic syndrome Liver disease
49
Why does megaloblasts occur?
Inhibition of DNA synthesis during red blood cell production
50
Cause of vitamin B12 deficiency?
``` Post gastrectomy/ileal resection Bacterial overgrowth Parasitic infection HIV infection Dietary deficiency Pernicious anaemia ```
51
Cause of folate deficiency?
Dietary deficiency Malabsorption Haemolysis Leukaemia
52
What is pernicious anaemia?
Autoimmune process against stomach Loss of glands, mucosal architecture and parietal and chief cells No intrinsic factor
53
Symptoms of vitamin B12 deficiency?
Normal anaemia symptoms Loss of vibratory sense and position Yellow-blue colour blindness Reflex loss
54
Management of megaloblastic anaemia?
Vitamin B12 before folate
55
Intravascular haemolytic anaemia?
Complement fixation | Trauma
56
Extravascular haemolytic anaemia?
Red cells removed from circulation by mononuclear-phagocytic system
57
Causes of haemolytic anaemia?
``` G6PD deficiency Hereditary spherocytosis Sickle cell Haemolytic uraemic syndrome TTP Autoimmune haemolytic anaemia HELLP ```
58
How to differentiate between autoimmune haemolytic anaemia and hereditary spherocytosis
Direct Coombs test ``` AHA = positive HS = negative ```
59
Types of sickle cell crises?
``` Thrombotic Sequestration Acute chest syndrome Aplastic Haemolytic ```
60
What is a thrombotic crisis?
``` Painful/vaso-occlusive Infection, dehydration, deoxygenation Infarcts occur in various organs e.g. Bone Hand-foot syndrome Lungs Spleen Brain ```
61
What is a sequestration crisis?
Sickling within organs causing blood pooling
62
What is acute chest syndrome?
``` Vaso-occlusive crisis of the lungs Fever Cough Sputum Tachypnoea Dyspnoea Hypoxia ```
63
What is an aplastic crisis?
Temporary cessation of erythropoiesis | Parvovirus B19
64
What is haemolytic crisis?
Sudden increase in haemolysis
65
What is von Willebrand's disease?
Most common inherited bleeding disorder | abnormality of vWF
66
What does vWF normally do?
Promotes normal platelet function | Stabilises factor VIII
67
What does APTT measure?
Intrinsic pathway Common pathway Including factors I, II, V, VIII, IX, X, XI
68
What does PT measure?
Extrinsic pathway Common pathway I, II, V, VII, X deficiency or effects of warfarin
69
Acute blood transfusion reactions?
``` Acute haemolytic reaction Infective shock Transfusion related lung injury Fluid overload Non-haemolytic febrile reaction Severe allergic reaction ```
70
What is acute haemolytic reaction?
``` Incompatible red cells with antibodies Leads to disseminated intravascular coagulation Low Hb High lactate High bilirubin ```
71
What is febrile non-haemolytic reaction?
Fever + rigors | Antibodies to white cells
72
Trasfusion related lung injury?
``` Acute respiratory distress Donor plasma has antibodies to leukocytes Non-productive cough Breathlessness Hypoxia Fever Rigors ```
73
Infective shock after blood transfusion?
Bacterial contamination of blood component
74
Delayed blood transfusion reactions?
Delayed haemolytic Alloimmunisation Post transfusion purpura GvHD
75
How long after transfusion for delayed haemolysis?
``` 5-10 days Fever low Hb Jaundice Haemoglobinuria ```
76
What is post-transfusion purpura?
Platelet specific alloantibodies | 5-9 days post transfusion
77
GvHD?
Mediated by T-lymphocytes Mortality rate 75-90% No treatment Irradiate blood prior to transfusion
78
Who is at risk of GvHD?
Immunodeficiency Allograft bone marrow and stem cell recipients Purine analogue Hodgkin's disease
79
Causes of splenomegaly?
``` non-Hodgkin's lymphoma Cirrhoesis Epstein-Barr virus Cytomegalovirus Cyst Haemangiomas CML Haematologic conditions ```
80
How to differentiate between lymphoblasts and myeloblast?
``` Myeloblast = auer rods or myelopersoxidase on staining Lymphoblast = TdT +ve on staining ```