Introduction to Haematology 22.09.2014 Flashcards

You may prefer our related Brainscape-certified flashcards:
1
Q

What would be the indications to look for erythrocytes, leukocytes, platelets and plasma on a haematology test?

A
  • Erythrocytes - anaemia, erythrocytosis (i.e. increased)
  • Leukocytes - inflammatory conditions, neoplastic conditiions, chemotheraphy
  • Platelets - bleeding disorders, DIC
  • Plasma - colour (normally colourless)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

How do you determine total protein?

A

Run a PCV, the put plasma into a refractometer to determine plasma protein

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Why would a stressed animal show a different PCV to normal?

A

The spleen releases stored RBCs when the animal is stressed.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

What variables are looked at in relation to RBCs? (7)

A

RBC concentration, HGB, HCT, MCV, MCH, MCHC, RDW (red cell distribution width)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

How is anaemia classified? (4) Why is it done these ways?

A
  1. ) Mild, moderate, severe
  2. ) MCV - normocytic, microcytic, macrocytic
  3. ) MCHC - normochromic, hypochromic, (hyperchromic)
  4. ) Regenerative vs. non-regenerative.

Helps narrow cause

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Examples of when you might see a normocytic anaemia.

A

Often associated with mild non-regenerative anaemia, acute haemorrhage etc,

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

When might you see microcytic anaemia? (3) Dog breed predisposition? (1)

A
Iron deficiency (allows an extra RBC division to ensure red cell haemoglobin concentration), PSS, hepatic failures. 
Akitas.
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

When might you see a macrocytic anaemia? Dog breed predisposition (1)

A

In regeneration.

Some poodles.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

When might you sees a normo- or hypochromic anaemia?

A

Decreased iron/poor iron incorporation (with microcytosis)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Why isn’t a hyperchromic anaemia not possible?

A

RBCs are haemolysed.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

2 reasons for regenerative anaemia

A

Haemolysis or haemorrhage

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Most common causes of non-regenerative anaemia (3)

A
  • Anaemia of inflammatory/chronic disease (mild, v. common)
  • CRF (severe)
  • Decreased production in marrow
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Differentiate polychromataphils and reticulocytes.

A

Same cells just different staining:

  • Polychromatophils: Diff-quik or giemsa stain, young cells containing rRNA show up as larger, bluer cells
  • Reticulocytes: same cells stained with New Methylene Blue and the RNA precipitates from aggregates (reticulum)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

How are cat reticulocytes different?

A

They are released as aggregate reticulocytes and mature to punctate retics over time. Retic. counts should record either aggregate or both.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

How do you differentiate between regenerative and non-regenerative aneamias? What are (ab)normal values?

A

Using the reticulocyte % (1000 RBCs counted, retics expressed as a percentage of this). Corrected reticulocyte % (same number of reticulocytes willt ake up more of a percentage in a very anaemic animal therefore calculate ritc %*(patient PCV/normal PCV).

NORMAL= 45% in dogs, 35% in cats
If regenerative>1% corrected (dog), >0.4% (cat)

Absolute reticulocyte concentration may be better:
RBC conc*retic%

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

What are the signs of regenerative anaemia on a blood smear? (7)

A

polychromasia, anisocytosis, macrocytosis, nRBCs, Howell-Jolly bodies, codocytosis, basophilic staining.

17
Q

What are different aspects of RBC morphology? (5)

A
  • Spherocytes, ghost cells
  • Hypochromasia/leptocytosis
  • Shear products (keratocytes, shistocytes, acanthocytes)
  • Oxidative damage (Heinz bodies, eccentrocytes, pyknocytes)
  • Organisms
18
Q

Which WBCs are considered in a CBC?

A

Neutrophils, lymphocytes, monocytes, eosinophils, basophils

19
Q

How can stress affect neutrophils?

A

Neutrophils normally circulate in the blood for approximately 6 hours but stress can cause neutrophils to move back from the tissue into the blood.

20
Q

What must be considered when looking at neutrophilia or neutropenia?

A

Ration of ProNP, MatNP and SNP. (i.e. look for left shift and toxicity)

21
Q

How is left shift classified?

A

REGENERATIVE: neutrophilia, segmented>bands
DEGENERATIVE: neutropenia, bands>segemented
In between?

22
Q

Which two ways can leukaemia be defined?

A

Acute/chronic or lymphoid/myeloid (i.e. lymphocytes vs neutrophils)

23
Q

How does clumping affect platelets?

A

It is a very common problem. It causes a decrease in platelet count/concentration as platelets aren’t evenly distributed in the fluid.

24
Q

Describe acute leukaemias

A

Blast cells in circulation (difficult to ID cell of origin). Much more likely to be lymphoid. ALL (acute lymphoid leukaemia) versus stage 5 lymphoma. If signs of segmentation = myeloid or myelomonocytic. Do immunophenotyping using a flow cytometer.

25
Q

Describe chronic leukaemias.

A
CLL = chronic lymphoid leukaemia; lymphocytes appear small and mature, persistant high numbers
CML = chronic myeloid leukaemia, neutrophils appear normal, persistant high numbers.
26
Q

How do you do a manual estimate of WBC numbers?

A

Average platelet number per 10 field, multiply by 15-20*10^9/L. Ensure you have a monolayer!