Cancer Flashcards

1
Q

Define o Anisocytosis

A

= unusual variation in RBC size

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2
Q

Cell size and colour in regenerative anaemia

A

Hypochromic macrocytosis
Also Polychromasia = blue/grey discolouration of large RBC

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3
Q

What can cause hyper chromic RBC

A

almost always due to haemolysis or lipaemia (raised MCHC is not physiologically possible due to restricted size of cells)

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4
Q

What to codocytes indicate

A

Target cells
Iron deficiency or liver disease

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5
Q

What do Acanthocytes indicate

A

Liver disease, splenic haemangioma or hemangiosarcoma or portosystemic shunts
Also high cholesterol diets

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6
Q

What do spherocytes indicate

A

IMHA
Transfusion reactions

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7
Q

What do Schistocytes indicate (Corn)

A

Disseminating intravascular coagulation (DIC),
thrombosis,
splenic hemangiosarcoma,
congestive heart failure,
immune mediated anaemia

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8
Q

Abnormal bodies: What are Heinz bodies?

A

Crystals of Hb on the outside of cells
Indicate oxidate damage like toxicity

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9
Q

Abnormal bodies: What is basophilic stippling?

A

= blue dots throughout cell
Associated with intensely regenerative anaemia or lead poisoning

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10
Q

Abnormal bodies: What do nucleated erythrocytes indicate?

A

Nuclear remnants
Due to regenerative anaemia, or marrow damage or non-functioning spleen

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11
Q

Abnormal bodies: What do Howell-Jolly bodies indicate?

A

Single, dark nuclear remnant
Regenerative anaemia, or after splenectomy/ reduced splenic function

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12
Q

name two RBC parasites

A

Babesiosis (TBF): Bi-lobed parasite
Mycoplasma haemofelis In cats

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13
Q

What is a stress leuckogram

A

Adrenaline and cortisol unsticks neutrophils from marginal pool so numbers increase
Stress leukogram = neutrophilia and lymphopenia and eosinopenia

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13
Q

What is a stress leuckogram

A

Adrenaline and cortisol unsticks neutrophils from marginal pool so numbers increase
Stress leukogram = neutrophilia and lymphopenia and eosinopenia

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14
Q

What do left shit neutrophils look like

A

More banded (less segmented)

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15
Q

What does toxic change look like

A

 Foamy cytoplasm, cytoplasmic basophilia, Dohle bodies (blue/grey cytoplasmic structures)
 Can be bands (D) or mature (B)

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16
Q

Reasons for lymphopenia

A

o Stress/steroids common reason
o Acute inflammation
o Loss of lymph

17
Q

which feline blood group has strong antibodies

A
  • Type B carry very strong anti-type A antibodies
18
Q

What is Feline neonatal isoerythrolysis

A

Type A/AB kittens born from a type B queen
Anti-A antibodies transferred in milk and attack kittens’ blood

19
Q

What blood groups are dogs broadly classed as

A

Dogs classed as either DEA1 positive (70%) or DEA1 negative

20
Q

Which blood transfusion is the only one that provides platelts

A

fresh whole blood

21
Q

when should you give frozen fresh plasma or frozen plasma?

A

FFP: contains ALL clotting factors

FP:: contains non-labile clotting factors (so not 5 and 8), good for coagulaotphy and haemophilia B

22
Q

Signs of anemia

A

Poor perfusion (Pale MM, lethargy, exercise intolerance)
Tachypnoea, tachycardia (compensatory)
Also: Icterus, weak + thready pulses, haemic murmur (diluted blood = less viscous)

23
Q

Indiactors of regneration

A

Macrocytic, hyper chromic cells
Polychromasia
nucleated RBCs, basophilic stippling, Howell-Jolley bodies

24
3 anaemia causes categories
Blood loss RBC destruction reduced bone marrow production (Non-regenerative)
25
most common form of anaemia and presentation
Anaemia of chronic disease is most common form to see. Normocytic, normochromic = normal cells, just not enough
26
Difference between true iron deficiency and functional
Functional: Bone marrow cannot incorporate iron into cells normocytic and normochronic True: loss of iron so not enough to go into cells seen in chronic haemhorrhage cells are hypo chromic and microcytic
27
Treatment for haemolysis
Immunosupression start with steroids
28
How to treat oxidative damage due to paracetamol
N-acetylcysteine
29
Treatment for Babesia or Enhrlichia
Doxycycline or imidocarb (unlicensed)
30
signs of primary haemostat disorders
* Petechiae/ecchymoses common * Bleeding from MMs (eyes, gingiva) * Often more than one site bleeding * Haematomas rare
31
signs of secondary haemastatic disorders
* Petechiae/ecchymoses rare * Deep/cavity bleeds * Sometimes a single site is bleeding * Haematomas common
32
Test for Petechiae
Does lesions blanch under microscope slide? o No = haemorrhage must be in skin = Petechiae
33
Common causes of primary haemostat disorders
Thrombocytopaenia: Low platelet numbers (Defective production in bone marrow or Accelerated removal (IMTP or DIC) , or Platelet sequestration or loss (Splenomegaly, vascular pooling, acute haemorrhage) Thrombocytopathia: Platelet dysfunction. Rarer caused by drugs or neoplasia. Dx: Normal platelet count but prolonged BMBT AND normal levels of VWF vWF deficiency: Common inherited disorder. Predisposed in Dobermans dx: Normal platelet count but slow BMBT AND low levels of VWF
34
What causes secondary haemostat disorders
* Issue with the coagulation pathway (intrinsic or extrinsic) * Requires various factors, factors, fibrinogen (F1) and vitamin K
35
What pathways do different tests... test
Whole blood clotting time: Intrinsic and common OSPT Aka Prothrombin time (PT): Extrinsic and common. Prolonged due to any factor Activated partial thromboplastin time (APTT): intrinsic and common. Prolonged due to a single factor.
36
Causes of secondary heamostatic disorders
Haemophilia - lack of factor 8 (APTT increased) Vitamin K antagonism - rodenticides Hepatic disease - all clotting factors produced in liver (APTT and OSPT increased)
37
Diagnostic sign of thrombosis (tertiary haemostat disorder)
Clot blocks vessel = hypoxia and tissue damage D-dimers produced during fibrinolysis so lots of fibrinolysis = lots of D-dimers
38
Homeostatic diagnostic summary (., 2, 3)
1. Platelet count, BMBT, platelet function, vWf 2. WBCT, APTT, OSPT, (specific factors) 3. D-Dimers (FDPs)
39
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