Haematology Flashcards

1
Q

isolated neutropaenia

A

hereditary, toxic, or immune cause

  • Benign ethnic neutropaenia
  • myelodysplastic malignancies
  • aplastic anemia
  • SLE, RA
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2
Q

Polycythaemia rubra vera can progress to …

A

myelofibrosis

AML

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3
Q

macrocytic, megaloblastic anaemia causes

A

vitamin B12 deficiency

folate deficiency

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4
Q

macrocytic, normoblastic anaemia causes

A
alcohol
liver disease
hypothyroidism
pregnancy
reticulocytosis
myelodysplasia
drugs: cytotoxics
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5
Q

disseminated intravascular coagulation what?

causes?

A

clotting factors used in small blood clots
–> purpura & petechia
but bleeding more likely
sepsis, trauma, malignancy

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6
Q

disseminated intravascular coagulation

A

↓ platelets
↓ fibrinogen
↑ PT & APTT
↑ fibrinogen degradation products

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7
Q

Aplastic anaemia

A

Pancytopenia (few all cells)

Hypoplastic bone marrow (nothing there hun)

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8
Q

Aplastic anaemia causes

A

Parvovirus, hepatitis
Radiation
Toxins - benzene
Cytotoxic, chloramphenicol, sulphonamides, phenytoin, gold

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9
Q

Autoimmune haemolytic anaemia

A

Warm/cold depending on antibodies

Can be secondary to lymphoproliferative, infection, drugs

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10
Q

Warm AIHA

A

IgG - haemolysis binds at body temp/37
extravascular sites - spleen

SLE, lymphoma, CLL, methyldopa

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11
Q

Warm AIHA treatment

A

Steroids

Immunosuppression Splenectomy

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12
Q

Cold AIHA

A

IgM - haemolysis - binds at 4 deg
Intravascular
- raynauds
- acrocyanosis

lymphoma, mycoplasma, EBV

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13
Q

Microcytic anaemia

A

Iron deficiency

Thalassaemia

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14
Q

Iron def anaemia sings

A

Koilonychia
Angular stomatitis
Plummer-Vinson

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15
Q

Iron def anaemia investigations

A

low ferritin, transferrin saturation

increased TIBC

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16
Q

Thalassaemia

A

inherited mutation to globing chain

haemolysis by spleen

17
Q

Macrocytic anaemia

A

B12, folate

Alcohol/liver

18
Q

folate deficiency

A

green veg, nuts
4 months
absorbed in proximal jejunum
treat w B12 & folate

19
Q

b12 role

A

meat, fish
absorbed in terminal ileum w IF (from gastric parietal cells)
needed for DNA/myelin synth

20
Q

b12 deficiency

A
  • gastrectomy, ideal resection, chrons, diet
  • anaemia
  • pallor, mild jaundice
  • glossitis
  • neuro - paraethesia, neuropathy
21
Q

pernicious anaemia

A

autoimmune atrophic gastritis
by ABS to parietal cells or IF

assoc w thyroid, vitiligo, addisons

risk of gastric adenocarcinoma

22
Q

Hereditary Spherocytosis

A

aut dom RBC membrane defect
spherocytes trapped in spleen

  • splenomegaly
  • pigment gallstones
  • jaundice
  • aplastic/megalobalstic crisis
23
Q

Sickle cell disease

A

B globin gene = glu –> val
HbSS (Trait - HbAS)

decreased life span
trapped - thrombosis

24
Q

Sickle cell complications

A

Sequestration crisis = splenic pooling, shock, severe anaemia

Splenic infarction

Aplastic crisis = Parvo b19

Gall stones

Osteomyelitis infection

25
Q

Haemophilia

A
A = factor 8 
B = factor 9 

X-linked
increased AAPT, normal P

26
Q

Von Willebrand disease

A

most common
vWF - binds plats via GpIb to damaged endothelium

increased APTT, bleeding

27
Q

bleeding disorder treatment

A

desmopressin
tranexamic acid

major & haemophilia rhF8