Microcytic Anemias Flashcards

1
Q

What is the definition of anemia?

A

Decreased oxygen transport due to red blood cells not supplying enough oxygen

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2
Q

What values do we see when Microcytic/Hypochromic anemia occurs?

A

MCV < 80
MCHC < 32%

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3
Q

What are factors affecting Iron levels?

A

Ingestion
Absorption
Recycled Hemoglobin
Stores
Loss

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4
Q

What are factors affecting iron Absorption?

A

Health of the Gastric Mucosa
Gastroesophageal Reflux Disease (GERD)
Current Iron Stores
Erythropoietic Need
Amount of Iron Ingested

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5
Q

How much iron is recycled for adults?

A

95%
1.0 mg for men and infants
2.0 mg for women

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6
Q

How much iron is recycled for infants?

A

70%
1.0 mg for infants

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7
Q

What are the causes related to Iron Deficiency Anemia (IDA)?

A

Increased Demands
Lack of Iron Intake
Nutritional Deficiency
Blood Loss

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8
Q

Pica, Cheilitis, and Koilonychia are representative of what?

A

Unique Symptoms of Iron Deficiency Anemia (IDA)

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9
Q

How do we test for IDA in a lab?

A

RBC status by CBC
Iron Status (Serum Iron, Total Iron Binding Capacity (TIBC))

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10
Q

Accumulation of iron in the mitochondria, resulting in Mitochondrial Overload is a cause of what?

A

Sideroblastic Anemia

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11
Q

Is Sideroblastic Anemia Acquired or Hereditary?

A

Both
Acquired: High Transfusion, Alcoholism, Lead Poisoning, Chloramphenicol
Hereditary: Enzyme Deficiency

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12
Q

How do we diagnose Sideroblastic Anemia?

A

Ringed Siderblasts

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13
Q

What does the abnormal gene HFE cause at a young age?

A

Hereditary Hemochromatosis (HH)
Autosomal Recessive Disorder

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14
Q

Cirrhosis of the liver, Diabetes, Swollen Joints, and Hair Loss are characteristic of what?

A

Hereditary Hemochromatosis (HH)

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15
Q

What are the specific diagnostic guidelines set by the CDC in relation to Hereditary Hemochromatosis (HH)?

A

Serum Ferritin Levels > 300 ug/L
Transferrin Saturation Levels >60% (45-60% = borderline)

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16
Q

What is the cause of Thalassemia?

A

Defect in Hemoglobin Synthesis
Lack of Alpha or Beta globin chain production

17
Q

What is the cause of Alpha Thalassemia?

A

Deletion of one or more alpha genes
A-chain is critical in adult Hb formation

18
Q

What is known as the complete absence of alpha globin chain synthesis?

A

Bart’s Hydrops Fetalis

19
Q

How is Hgb Bart’s created?

A

4 gamma globin chains
Spontaneous abortion and stillbirth

20
Q

How is Hemoglobin H Disease acquired?

A

3 gene deletion, 1 functional A chain
RBC resembles a pitted golf ball

21
Q

What is known as having two functional alpha genes that is usually seen with mild anemia?

A

Alpha Thalassemia Trait

22
Q

What is known as having three functional alpha genes and is hematologically normal?

A

Silent Carrier

23
Q

Beta Thalassemia Major aka Cooley’s/Mediterranean Anemia is caused by?

A

Little or no Beta globin chain synthesis

24
Q

What is known as One abnormal beta gene that is inherited heterozygously?

A

Beta Thalassemia Trait (Minor)
Mimics IDA
Basophilic Stippling
Target cells