Haematology Flashcards

1
Q

Microcytic Anaemia:

Causes

A
Iron deficiency anaemia
Thalassaemia
Sideroblastic anaemia (rare)
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2
Q

Normocytic anaemia:

Causes

A
Acute blood loss
Anaemia of chronic disease
Bone marrow/renal failure
Hypothyroid
Haemolysis
Pregnancy
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3
Q

Macrocytic anaemia:

Causes

A
B12/folate deficiency
Alcohol/liver disease
Reticulocytosis
Drugs/toxins
Hypothyroidism
Myelodysplastic syndromes
Marrow infiltration
Anti folate drugs eg phenytoin
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4
Q

Iron deficiency anaemia:

Signs

A

Glossitis
Angular stomatitis
Koilonychia

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5
Q

Anaemia:

symptoms & treatment

A
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6
Q

Polycythaemia:

Causes

A

Dehydration (alcohol, diuretics)
Obesity+alcohol+smoking+HTN
Hypoxia (altitude, chronic lung disease, cyanotic heart disease, heavy smoking)
Cancer (over secretion of erythropoietin)

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7
Q

Polycythaemia:

Management

A

Venesection
Daily lose dose aspirin
Hydroxycarbamide (>60 men)
(Interferon childbearing age women)

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8
Q

Thrombophilia:

Causes

A

Post op
Infection
Inflammation

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9
Q

Neutrophilia:

Causes

A

Infection
Vasculitis
Inflammation
Malignancy

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10
Q

Lymphocytosis:

Causes

A

Viral infection
CLL
ALL

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11
Q

Lymphopenia:

Causes

A

Drugs
Infection
Autoimmune (SLE)

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12
Q

DIC

A

Widespread release of proagulants into system causes widespread clotting then use up of all clotting factors and platelets leading to widespread bleeding

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13
Q

DIC:

Causes

A

Malignancy
Sepsis
Trauma
Obstetrics

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14
Q

DIC:

Signs and Tx

A
Bruising and bleeding everywhere
Renal failure
⬇️platelets
⬆️PT
⬇️ fibrinogen
⬆️ d dimer

Tx
Replace platelets and clotting factors

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15
Q

Von Willebrands Findings

A
Slightly prolonged APPT
Normal/prolonged PT
Autosomal dominant
Menorhhagia/epistaxis
Factor VIII
petechial rash
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16
Q

Unprovoked DVT/PE

A

3 months VKA

17
Q

Provoked DVT/PE

A

6 months VKA

18
Q

bilobed large mononuclear cells + bleeding

A

AML

19
Q

AML

A
Adults
Auer Rods
DIC/thrombocyotopaenia
bilobed mononuclear
low WCC
low platelets
20
Q

Von Willebrands Findings

A
Slightly prolonged APPT
Normal/prolonged PT
Autosomal dominant
Menorhhagia/epistaxis
Factor VIII
21
Q

Unprovoked DVT/PE

A

3 months VKA

22
Q

Provoked DVT/PE

A

6 months VKA

23
Q

bilobed large mononuclear cells + bleeding

A

AML

24
Q

AML

A
Adults
Auer Rods
DIC/thrombocyotopaenia
bilobed mononuclear
low WCC
low platelets
25
Q

Causes of thrombophilia

most to least common

A
Factor V Leiden
Protein C deficiency
Protein S deficiency
Antithrombin III deficiency
Antiphospholipid
26
Q

Polycythaemia Rubra Vera

A

JAK2
hyperviscocity, pruritis after bath, splenomgaly, haemorrhage, plethora
high haemoglobin low neutrophils low ESR

27
Q

CML

A

Elderly

Well differentiated B cells

28
Q

Factor V Leiden

A

Activated protein C resistance

Inherited

29
Q

Beta thalassaemia trait

A

Autosomal recessive
Hypochromic microcytic mild anaemia
HbA2 raised

30
Q

Haemophillia

A

X-linked recessive
A - Factor VIII deficiency
B - IX

prolonged bleeding, haemarthrosis

31
Q

Polycythaemia Rubra Vera

A

JAK2
hyperviscocity, pruritis after bath, splenomgaly, haemorrhage, plethora
high haemoglobin low neutrophils

32
Q

tear drop poikilocytes

A

myelofibrosis

33
Q

Test for spherocytosis

A

Osmotic fragility