Pathology Exam- Anemia 2 Flashcards

1
Q

Reasons for nutritional anemia?

A
  • vitamin B12 and folic acid deficiency
  • iron deficiency
  • copper deficiency
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2
Q

Reasons for hypoproliferative anemia?

A
  • inflammation or chronic disease
  • chronic renal or hepatic failure
  • neoplasia
  • endocrine disease
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3
Q

What is megaloblastic anemia?

A

Due to vitamin B12 and folic acid deficiency
- leads to low proliferation and differentiation of erythroblast
Causes:
- diet deficiencies
- malabsorption syndrome
- high requirements (pregnancy, lactation)
-chemoteraphy and anticonvulsion teraphy
Pathophysiology:
-inhibition of DNA synthesis= inefficient erythropoiesis
-macrocytic and normochromic
Diagnosis:
-big RBCs
-megaloblasts, erythroblasts
-hyper segmented neutrophils

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4
Q

What is iron deficiency anemia?

A
Lack of iron needed for Hb synthesis
Causes:
-chronic bleeding
-low iron intake
-malabsorbtion
- high consumption in nursing animals
Normo- or microcytic, normo- or hypochromic anemia
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5
Q

What is copper deficiency anemia?

A

Copper is required to absorb and release iron
Signs:
-Neurological=“swayback”, hematological signs
-low growth rates
- GI signs

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6
Q

What are anemia’s of inflammation/chronic disease?

A
  1. High inflammatory cytokines
    -reduces iron availability
    - inhibition of EPO production/release
    - decreased biological activity of EPO2. Decreased RBC lifespan
    Normochromic, normocytic mild anemia
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7
Q

What is anemia’s due to neoplasia?

A
Could be due to:
- chronic disease
-blood loss
- immune mediated hemolysis
- chronic antineoplastic treatment
Inflammatory anemia: normochromic, normocytic
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8
Q

What is anemia due to renal disease?

A

Causes:

  • deficiency in EPO
  • effects of uremic toxins (GI ulcers, suppression BM, urea)
  • chronic inflammatory disease
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9
Q

What is anemia of liver disease?

A
  • anemia of chronic disease
  • interference with EPO synthesis
  • alteration of iron metabolism
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10
Q

What is anemia of endocrine disease?

A

Most endocrinopathies cause mild anemia

  • diabetes mellitus (ketoacidosis=oxidative damage)
  • hypothyroidism (generalized decrease in metabolism= low EPO, low proliferation in BM)
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11
Q

What are the types of primary BM anemia?

A

Aplastic= destruction of BM hematopoietic cells
- pancytopenia
- pure red cell aplasia
Mieloptisis= BM infiltration
- myeloproliferative or lymphoprilferative diseases

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12
Q

What is pancytopenia in aplastic anemia?

A
Clinical syndrome, BM doesn’t produce blood cells at all
Features:
- pancytopenia
- replacement of normal BM cells by fat
Causes:
- infection
- drugs
- immune mediated
Acute or chronic, BM biopsy
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13
Q

What is red cell aplasia in aplastic anemia?

A
Involves only red cell precursors
Findings:
- normocytic, normochromic anemia
- reticulocytopenia
- absence of red cell precursors in BM aspirate
- white cells are normal
Causes:
- immune mediated
- infectious
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14
Q

What is polycythaemia/erythrocytosis?

A

Absolute increase in RBC mass
- increased HCT and Hb concentration
- high RBC count, Hb and HCT
Relative or absolute

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15
Q

What is relative polycythaemia?

A
  • Decrease in plasma volume relative to no of RBCs
  • increase of concentration of RBCs due to loss of plasma
  • haemogram= high PCV, high TP
    1. Haemocincentration
  • dehydration
  • diarrhea
  • burns
    2. Splenic contraction in horses and greyhounds
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16
Q

What is absolute polycythemia?

A

Polycythaemia Vera:
- myeloproliferative disorder with abnormal increase in RBCs
- serum EPO activity is usually low
Secondary polycythaemia:
- physiological due to compensatory tissular hypoxia (hypoxia driven)
- non physiological due to pathological high EPO (hypoxia independent)

17
Q

What are the consequences of erythrocytosis?

A
Hyperviscosity syndrome:
- spontaneous bleeding from mucous membranes
- visual disturbances (retinopathy)
- neurological signs
Heart failure
Hypoxia