Haematology Flashcards

(49 cards)

1
Q

Macrocytic anaemia 3 DDx

A
deficiencies of folate and vitamin B12, 
liver disease
alcohol excess
untreated hypothyroidism
myelodysplastic syndromes
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2
Q

macrocytic anaemia 3 Ix

A

B12/folate
thyroid functions tests
liver function tests
blood film to confirm macrocytosis and exclude myelodysplastic syndrome

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3
Q

Diet that often -> b12 deficiency?

A

vegan

[b12 in meat and dairy]

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4
Q

Pernicious anaemia is?

mx?

A

autoimmune condition with antibodies directed
against gastric parietal cells or intrinsic factor itself,
-> prevents absorption and binding of B12 from the diet

intramuscular hydroxycobalamin

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5
Q

Mx sickle cell crisis

A

high-flow oxygen, intravenous
fluids, thromboprophylaxis, antibiotics

consider transfusion

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6
Q

Why abx in sickle cell crisis

A

sickle cell patients will have autoinfarcted their spleen
in childhood, rendering them functionally
asplenic

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7
Q

3 causes of pleuritic chest pain

A
  • Pleural inflammation secondary to bacterial or viral chest infections
  • Pulmonary embolus
  • Asthma
  • Rib fractures/pathology
  • Subphrenic abscess/intra-abdominal sepsis
  • Lung masses
  • Connective tissue disorders/autoimmune disorders
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8
Q

Biochem common findings with upper GI bleed

A

acute - raised platelets
Urea raised - [more than creatinine]
Anaemia

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9
Q

Initial Mx of upper GI bleed ? After resus? Scoring system for upper GI bleed mortality?

A

good venous access (minimum of two large-bore cannulae),
Bloods FBC, LFT, clotting tests,
Group and save, and a cross-match for four units of packed red cells.
Volume replaced with colloid

After resus
All anticoagulants, antiplatelets, NSAIDs stopped
High dose PPI
Endoscopy within 24hrs

Rockall score

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10
Q

Name 3 causes of upper GI bleed

A
–– Peptic ulcer disease
–– Oesophagogastric varices
–– Arteriovenous malformations
–– Mallory–Weiss tears
–– Tumours and erosions
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11
Q

Main DDx in an older person with normocytic anaemia

A

• Anaemia of chronic disease
• Most haemolytic anaemias
• Mixed causes of anaemia
- [If Iron and folate/b12 deficient it is possible that they ‘cancel’ each other out leading to a normal MCV]

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12
Q

Name 2 congenital causes of haemolytic anaemia

A

sickle cell disease,
thalassaemia,
glucose-6-phosphate dehydrogenase deficiency,
hereditary spherocytosis

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13
Q

Name 3 acquired causes of haemolytic anaemia

A
Autoimmune
infections – particularly Mycoplasma pneumoniae or Clostridium perfringens
sepsis, 
drugs, 
burns, 
metallic heart valves
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14
Q

Basic bloods / Hx make you suspicious of autoimmune anaemia - what further Ix do you want?

A
blood film, 
reticulocyte count, 
Coombs’ test, 
unconjugated bilirubin 
LDH
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15
Q

In autoimmune haemolytic anaemia, what provokes

their uptake by the reticuloendothelial system and promote red cell haemolysis

A

RBCs are coated in either

antibodies (IgG) or complement (C3d)

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16
Q

2 main DDx in rapid onset anaemia

A

bleeding

autoimmune

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17
Q

Mx of autoimmune haemolytic anaemia

A

remove any precipitating cause, and immunosuppression
with high-dose steroid therapy
[can add ciclospoin / azathioprine….. transfusion may be indicated]

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18
Q

Name 3 DDx of pancytopenia

A
Post-chemotherapy (transient)
• Haematinic deficiency (B12 or folate)
• Autoimmune conditions
• Sepsis
• Bone marrow infiltration from lymphoma or other metastatic malignancy
• Myelodysplastic syndrome
• Acute or chronic leukaemias
• Acute viral infections
• Drug induced
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19
Q

Peripheral lymphocytosis DDx

A

ALL, CLL, Lymhoma

EBV, CMV

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20
Q

three most common causes for bilateral hilar lymphadenopathy

A

Sarcoidosis
lymphoma
TB

21
Q

name 3 causes of raised LDH

A
  • Myocardial injury
  • Malignancy (especially lymphoma)
  • Liver disease
  • Lung disease
  • Haemolysis
22
Q

DDx of thrombocytopenia

A
  • Immune thrombocytopenic purpura
  • Drug-induced thrombocytopenia
  • Acute viral infection (e.g. HIV, hepatitis C)
  • Sepsis
  • Underlying haematological malignancy/myelodysplastic syndrome
23
Q

Immune thrombocytopenic purpura
Lab findings?
Mx?

A

Low platelets - all other results normal [unless bleeding -> anaemia]

Steroids
-transfusion not indicated unless major haemorrhage

24
Q

Treatment of DVT in pregnancy

A

LWMH - usually continue throughout pregnancy

25
Antibiotic that interacts with warfarin?
macrolides - erythromycin / clari inhibit metabolism of warfarin -> increased INR
26
Post surgery - sudden thrombocytopenia... What drug are you worried has caued? Other DDx?
herparin -> heparin induced thrombocytopenia [autoimmune agaist heparin bound to platets] [Usually occurs 5–14 days after exposure to heparin] sepsis / infection ITP
27
Anaemia with splenomegaly, thrombocytosis and a raised LDH Dx? Usual mutation? Mx?
myleofibrosis JAK2 Supportive - analgesia / transfusion if required JAK2 inhibitors [very few in development] Definitive - allogenic stem cell transplant
28
What is meant by apparent polycythemia? true Pimary vs secondary ? mx?
decrease in plasma volume -haematocrit increases Primary - myeloproliferative neoplasm usually JAK2 Secondary - Increased erythropoietin production Venesection hydroxycarbamide, - reduce platlet count
29
Causes of secondary polycythemia
* Chronic hypoxia (lung disease, heart disease, high altitude) * Long-term smoking * Abnormal haemoglobins * Increased erythropoietin production (renal tumours, other malignancies)
30
Myelofibrosis features? Key cell? Differentiate from CML
fibrosis and ineffective erythropoiesis / marrow failure Massive hepatosplenomegaly Tear drop (dacrocytosis) NO philidelphia chromosome
31
Smear cells in
CLL
32
B Sx
fever, night sweats, and weight loss
33
Suspicious of lymphoma - Key things you'll look for OE
lumps at lymph nodes | Hepato / splenomegaly
34
Staging of lymphoma
ann arbour
35
Name 3 signs pf iron deficient anaemia OE
``` Tachy cardia /pnea Pallor Ejection systolic murmur angular cheilitis atrophic glossitis spoon shaped nails ```
36
bar microcitic anaemia what other blood test findings in iron deficiency
low serum ferritin | raised total iron binding capacity
37
Long term drugs sickle cell
hydroxyurea (hydroxycarbamide) penicilin folic acid
38
most common Ig in myeloma
IgG
39
3 Acute complications of myeloma
hypercalcaemia spinal cord compression hyperviscosity acute renal failure
40
2 Reasons why myeloma pt susceptible to infection
Bone marrow infiltration | Overexpression of 1 Ig -> Underexpression of others
41
Drug and class for CML
imatinib - tyrosine kinase inhibitor (oral)
42
What Hb level for transfusion regardless of Sx
<7g/dL
43
2 Early and Late complications of transfusion
``` Early - Acute haemolytic reaction allergic / anaphylaxis Transfusion related acute lung injury fluid overload ``` ``` Late Iron overload GVHD Infection post transfusion purpura ```
44
What is a massive transfusion?
transfusion of the entire volume of blood / 10 units in 24 hours
45
2 types of macrocytic anaemia and an eg of each
megaloblastic - B12/folate deficiency, cytotoxic drugs Non-megaloblastic - alcohol, liver disease, hypothyroid, pregnancy, reticulocytosis
46
Ix for pernicious anaemia | mX
parietal cell / intrinsic factor antibody serology shilling test IM hydroxycobalamin
47
Mx options Haem A
Factor VIII | Desmopressin
48
How could a 70-year-old lady be Dx with Haemophilia
Aquired - autoantibodies to factor VIII
49
When do you get alcohol induced pain
lymphoma