BIIC Pathology Lecture 3_Microcytic, Macrocytic, and Aplastic Anemias Flashcards

1
Q

What is transferrin?

A

It is an iron binding protein that is created in the liver and transports dietary iron through the blood to the locations of heme production

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2
Q

In healthy individuals, what is the typical transterrin saturation and serum iron levels for men and women?

A

1/3 transferrin saturation. 120 ug/dL serum iron in men and 100 mg/dL serum iron in women

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3
Q

What is ferritin?

A

It is a protein iron complex found in the spleen, bone marrow, liver, and skeletel muscle

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4
Q

What are the 4 microcytic anemias?

A

Iron deficency
Anemia of chronic disease
Thalassemia
Sideroblastic anemia

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5
Q

What are the two macrocytic anemias?

A
Folate deficiency (vitamin B9)
Vitamin B12 dificiency (cobalamine)
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6
Q

What is the most common nutritional deficency in the world?

A

Iron deficiency

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7
Q

What are the 4 mechanisiums that result in insuficient nutriant in the body?

A

1) dietary lack
2) Malabsorbtion
3) Increased demands (cancer)
4) Blood loss

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8
Q

What percentage of ingested iron is absorbed into the body? What is the required daily intake for men and women?

A

Only 10-15% of ingested iron is absorbed. Men need 7-10mg daily and women need 7-20 mg (premenopause women are on the higher end)

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9
Q

What conditions can cause malabsorbtion of Iron?

A

sprue, chronic diarrhea, gastrectomy, and celiacs.

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10
Q

What is the most common cause of iron deficiency in the developed world? What clinical significance does this have?

A

Chronic bleeding is the most common cause. This means, any iron deficency in men or postmenopausal women must be treated as a GI bleed until proven otherwise

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11
Q

What are Four key clinical findings in iron deficiency anemia?

A

low serum iron levels, low ferritin level, and low transferrin saturation, and disappearance of stainable iron bone marrow macrophages (this is seen with prussian blue stains).

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12
Q

What are the three histologic findings of iron deficiency anemia?

A

expanded cental palor, hypocromatic, and poikilocytosis (pencil cells)

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13
Q

What is the most common anemia in hospitalized patients

A

anemia of chronic disease

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14
Q

What is the MOA of Anemia of chronic Disease

A

Inflammatory cytokines like IL-6 cause elevated levels of hepcidin which block the transfer of iron to erythroid precursers and thus suppress erythropoesis

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15
Q

What is the MOA of Macrocytic anemias?

A

Both folate and B12 are required for DNA synthesis (they are required to make thymidine). Without them DNA syntheis does not occure and this is seen most quickly in rapidly dividing cells. Because this effects the megaloblastic stem cells, this is often causes pancytopenia (low count of RBC, WBC, and platlets)

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16
Q

What are two histologic findings of Macrocytic anemia? Which is the “early finding”

A

Macrocytic anemia presents with hypersegmented neutophils (an early finding) and macroovalocytes (egg shaped RBCs)

17
Q

What is the main cause of folate deficiency

A

typically inadequate dietary intake

18
Q

How does the manifestation of B12 deficiency differ from folate?

A

B12 Deficiency will often present with neurological banormalities (caused by demylination) as well.

19
Q

How can folate and and B12 macrocytic anemias be distinguished?

A

Measure serum and RBC levels of folate and B12

20
Q

How do B12 deficiencies typically arise?

A

They are most often a result of malaborbtion (can be intake in diets with no animal products)

21
Q

How many years of B12 can your liver store

A

5-20 years worth

22
Q

What is the main cause of malabsobtion of B12?

A

Perniciouse anemia which is an auto immune attack on the gastric mucosa so intrinsic factor is not produced and B12 is not absorbed. Other causes are gastrectomy, ileal resection, and conditions that effect the distal ilium like crohn’s

23
Q

What are the neurologic results of B12 deficiency?

A

Demylination of the posterior and lateral columns of the spinal cord.

24
Q

What is aplastic anemia?

A

It is a disorder in which multipotent myeloid stem cells are suppressed leading to pancytopenia. Histology of bone marrow is often devoid of hematopoetic elements

25
Q

What is the MOA of aplastic anemia?

A

65% of cases are idiopathic although some chemicals are known to cause it (benzene, chemotherapy) as well as some viral infections

26
Q

What is Fanconi anemia

A

A rear inherited aplastic anemia characterized by Marrow hypofunction becomes evident early in life, often accompanied by multiple
congenital anomalies, eg, hypoplasia of the kidney and spleen and bone anomalies,
which most commonly involve the thumbs or radii

27
Q

How does inherited defects of telomerase cause aplastic anemia?

A

The telomeres shorten prematurely and therefor become non functional leading to non functional hematopoetic precursors due to premature senescence

28
Q

What are the two major MOA of aplastic anemia?

A

✴ An extrinsic, immune-mediated suppression
of marrow progenitors
✴ An intrinsic abnormality of stem cells

29
Q

What is Pure Red Cell Aplasia

A

It is a condition where only RBC precursors are suppresed. Can be autoimmune or a result of parvo B19

30
Q

What is Myelophthistic Anemia

A

This is when hematopoesis is stopped because bone marrow is replaced by a space occupying legion

31
Q

How does renal failure cause anemia?

A

The kidney is what produces EPO. Without the kidney there will be now erythropoesis