Exam Review-quick Flashcards

1
Q

WHich type of anemia has a HIGH TIBC?

A

Iron deficient

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2
Q

What type of anemia has normal or high ferritin, high ESR/CRP?

A

Anemia of chronic disease

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3
Q

Number one cause of Fe deficient anemia

A

Bleeding

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4
Q

Patho of anemia of chronic diseasE?

A

Increased IL-6, increased hepcidin, Fe stuck in liver and cant get out to serum

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5
Q

What types of cells are seen in alpha thalassemia?

A

HEINZ BODIES, target cells

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6
Q

What is the treatment for alpha thalassemia? And beta

A

Splenectomy, SCT, iron chelation, transfusions, folic acid supplements

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7
Q

What are the types of cells seen in beta thalassemia?

A

Dacrocytes, basophilic stippling, poikilocytosis

Also see target cells

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8
Q

Which type of anemia has DECREASED TIBC?

A

Sideroblastic

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9
Q

What types of cells are seen on sideroblastic anemia?

A

Pappenheimer bodies

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10
Q

What two drugs can cause sideroblastic anemia?

A

Chloramphenicol and linezolid

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11
Q

What type of anemia has abnormal spectrin and ankyrin?

A

Hereditary spherocytosis

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12
Q

What type of anemia has deficient CD55 and CD59 proteins?

A

PNH

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13
Q

Which type of anemia has episodic hemoglobinuria, thrombosis?

A

PNH

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14
Q

What is the treatment for PNH?

A

Eculizumab and corticosteroids

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15
Q

Which type of anemia has bite cells, blister cells, and Heinza bodies?

A

G6PD Deficiency

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16
Q

What drugs do you need to stay away from with G6PD?

A

Dapsone, Nitro, Bactrim, fava beans too

17
Q

What are some lab results for AIHA?

A

Sphrerocytes, NRBCs, + Coombs test, reticulocytosis

18
Q

Patho of AIHA?

A

IgG “warm” bind to RBCs

19
Q

What do you use to treat AIHA?

A

Prednisone

20
Q

What will labs show for cold Agglutinin?

A

Coombs + for IgM complement only, reticulocytosis, + cold Agglutinin titer

21
Q

What are the treatments for cold Agglutinin?

A

Avoid cold, Rituximab

22
Q

Rituximab

A

Treatment for cold Agglutinin

23
Q

Eculizumab

A

Treatment for PNH

24
Q

Howell-jolly bodies

A

Sickle cell anemia

25
Q

Substitute valine for glutamic acid in 6th AA

A

Sickle cell anemia

26
Q

Increased HbS?

A

Sickle cell anemia

27
Q

What is the treatment for sickle cell?

A

Hydroxyurea and omega-3 fatty acids, allergenic SCT with HLA matched donor

28
Q

Injury to pluripotent stem cell

A

Aplastic anemia

29
Q

What are some lab results for aplastic anemia?

A

Pancytopenia, nor abnormal hematopoietic cells, hypocellular bone marrow

30
Q

Moderate aplastic anemia

A

<30% cellularity, 2/3 blood elements decreased

31
Q

Severe aplastic anemia

A

<25% cellularity, retics <40,000 neutrophils <500 platelets <200

32
Q

Very severe aplastic anemia?

A

Same as severe except neutrophils <200

33
Q

VitB12 deficiency lab smear

A

Macroovalocytes, hypersegmented neutrophils, high MMA and homocysteine

34
Q

VitB12 si/sx

A

NEURO issues: decreased vibration, proprioception, memory issues

35
Q

Folic acid deficiency happens in who?

A

Alcoholics

36
Q

Smear for folic acid deficiency?

A

Megaloblastic smear, macroovalocytes and hypersegmented neutrophils, high homocysteine