Tales from the Haematology Clinic: RBC Flashcards

1
Q

what does WBC stand for?

A

white blood cell count in a given volume of blood

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2
Q

what does RBC stand for?

A

red blood cell count in a given volume of blood

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3
Q

Hb?

A

haemoglobin concentration

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4
Q

Hct?

A

haematocrit (packed cell volume)

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5
Q

MCV? units?

A

mean cell volume (i.e. how large a cell is)
calculation:
divide total volume of red cells by number of red cells
=
Hct/RBC
units = fl

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6
Q

MCH?

A

mean cell haemoglobin
=the amount of haemoglobin in a given volume of blood divided by the number of red cells in the same volume
Hb/RBC

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7
Q

MCHC?

A

mean cell haemoglobin concentration
Hb/Hct

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8
Q

platelet count

A

the number of platelets in a given volume of blood

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9
Q

FBC?

A

=full blood count
frequently performed blood test, often requested routinely in GP surgeries and hospitals

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10
Q

anaemia meaning?

A

reduction in the amount of haemoglobin in a given volume of blood, below what would be expected

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11
Q

signs of anaemia?

A

Hb is reduced
RBC and Hct/PCV are usually reduced as well

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12
Q

mechanisms of anaemia?

A

RBC failure of production
RBC excess loss/destruction

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13
Q

microcytic?

A

RBC that is smaller than usual, also usually hypochromic (central pallor <1/3)
happens due to lower haemoglobin content and flatter cell

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14
Q

normocytic?

A

normal red cell

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15
Q

macrocytic?

A

usually also normochromic

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16
Q

poikilocytes?

A

abnormally shaped RBC

17
Q

elevated HbA2?

A

B thalassemia trait

18
Q

difference between iron deficiency and thalassaemia?

A

MCHC is low in iron deficiency but relatively preserved in thalassaemia
RBC is low in iron deficiency but increased in thalassaemia trait
Hb electrophoresis is normal for iron deficiency but Hb A2 is raised in B-thal trait

19
Q

common causes of microcytic anaemia

A

-defect in haem synthesis
-defect in globin synthesis (thalassaemia)
this defect will be in a/b chain haemoglobin depending on type of haemoglobin

20
Q

causes of haemolytic anaemia?

A

-membrane (hereditary spherocytosis)
-haemoglobin defects (HbSS)
-cellular metabolism (G6PD deficiency)

21
Q

polychromasia?

A

bluish tinge due to cell cytoplasm
= young red cell, due to increased erythropoiesis
polychromatic cells are also larger than normal red blood cells

22
Q

normocytic anaemia?

A

recent blood loss - gastrointestinal haemorrhage, trauma
failure of production of RBC - e.g. bone marrow failure
pooling of red cells in the spleen - hypersplenism

23
Q

symptoms of sickle cell?

A

anaemia
jaundice
gallstones
among many other symptoms
e.g. vaso occlusion - bone, kidney, retina

24
Q

why do symptoms of anaemia not show in HbSS?

A

HbS is a low affinity haemoglobin

25
Q

spleen in sickle cell disease?

A

repeated occlusion of spleen leads to functional hyposplenism

26
Q

blood film of sickle cell anaemia?

A

sickle cells
boat cells
target cells
Howell-jolly bodies