Physiology of blood cells and haematological terminology Flashcards

(38 cards)

1
Q

Anisocytosis

A

Red blood cells show more variation in size than is normal

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2
Q

Poikilocytosis

A

Red blood cells show more variation in shape than is normal

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3
Q

Microcytosis

A

Red blood cells are smaller than normal

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4
Q

Macrocytosis

A

Red blood cells are larger than normal

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5
Q

Leucocytosis

A

Too many white blood cells

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6
Q

Leucopenia

A

Too few white blood cells

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7
Q

Neutrophilia

A

Too many neutrophils

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8
Q

Neutropenia

A

Too few neutrophils

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9
Q

Lymphocytosis

A

Too many lymphocytes

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10
Q

Eosinophilia

A

Too many eosinophils

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11
Q

Thrombocytosis

A

Too many platelets

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12
Q

Thrombocytopenia

A

Too few platelets

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13
Q

Erythocytosis

A

Too many Red blood cells

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14
Q

Reticulocytosis

A

Too many reticulocytes

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15
Q

Lymphopenia/Lymphocytopenia

A

Too few lymphocytes

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16
Q

Atypical lymphocyte/atypical mononuclear cell

A

Abnormal lymphocyte

-seen in infectious mononucleosis (glandular fever)

17
Q

Left shift

A

Increase in non-segmented neutrophils or neutrophil precursors in the blood

  • from inflammation or infection
  • band cells with no segmentation indicate rapid production during infection
18
Q

Toxic granulation

A

Heavy granulation of neutrophils

from infection, inflammation, tissue necrosis and pregnancy

19
Q

Hypersegmented neutrophil

A

increase in average number of neutrophil lobes

- from vitamin B12/folic acid deficiency

20
Q

Howell-Jolly body

A

Nuclear remnant in a RBC

-common cause=lack of splenic function

21
Q

Red cell agglutinates

A

Irregular clumps of RBCs (not tidy stacks)

  • from antibody on cell surface
  • sticks better in cold temperatures
22
Q

Rouleaux

A

Stacks of RBCs

-from alterations in plasma proteins

23
Q

Fragments/schistocytes

A

Small pieces of Red blood cell

-indication cell has fragmented

24
Q

Sickle cells

A

crescent shaped

-from Hb S polymerisation when it is present in high concentrations

25
Elliptocytes
Elliptical shaped | -seen in hereditary elliptocytosis and iron deficiency
26
Target cells
accumulation of haemoglobin in the centre of the central pallor area -from obstructive jaundice, liver disease, haemoglobinopathies, hyposplenism
27
Poikilocyte shape variety
- spherocytes - irregularly contracted cells - sickle cells - target cells - elliptocytes - fragments
28
Polychromasia
Increased blue tinge to RBC cytoplasm | -indication of young RBCs
29
Irregularly contracted cells
Irregular outline, smaller than normal, no central pallor | -from oxidant damage to cell membrane and haemoglobin
30
Spherocytes
~spherical shaped, regular outline, no central pallor - from cell membrane loss without equivalent cytoplasm loss so cell forced to round up - seen in hereditary spherocytosis (not all spherical cells)
31
Hypochromia
larger area of central pallor than normal (normal ~1/3 diameter pale) - normal pallor from disc shape (less Hb in centre) - hypochromia from lower Hb content and concentration and flatter cell - often seen with microcytosis - 'hypochromic' RBCs
32
Hyperchromia
Cells lack central pallor -from abnormal shape or being thicker than normal (can have many causes as abnormally shaped cells often lack a central thinner area) -'hyperchromatic'/ 'hyperchromic' RBCs
33
Macrocytic
RBCs are larger than normal or anaemia with large RBCs (lymphocyte as reference material)
34
Normocytic
RBCs are normal size or anaemia with normal sized RBCs (lymphocyte as reference material)
35
Microcytic
RBCs are smaller than normal or anaemia with small RBCs (lymphocyte as reference material)
36
Microcyte
Red blood cell that is smaller than normal
37
Macrocyte
RBC that is larger than normal =large erthyrocyte | -variety of types (round macrocytes, oval macrocytes, polychromatic macrocytes)
38
Right shift
Increase in number of neutrophil lobes