ACE THIS EXAM GIRL! Flashcards

1
Q

Most common cause of anemia worldwide?

A

iron deficiency anemia

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2
Q

Most common cause for iron deficiency anemia?

A

bleeding

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3
Q

Spoon nails, cheilosis

A

iron deficiency anemia

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4
Q

Microcytosis, normal iron level and family hx

A

Thalassemia

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5
Q

What is the definitive dx for sideroblastic anemia?

A

bone marrow

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6
Q

Macrocytic anemia

A

Vitamin B12

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7
Q

What is the number 1 cause of Vit B12 deficiency?

A

inability to absorb

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8
Q

What test determines the underlying cause of anemia?

A

Shilling TEST

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9
Q

Most common cause of folate deficiency

A

inadequate dietary intake

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10
Q

Diagnostic RBC folic acid level?

A

<150 mg/ml

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11
Q

African African males and Mediterranean population

A

G6PD

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12
Q

Fava beans

A

G6PD

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13
Q

Heinz Bodies

A

G6PD

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14
Q

Primary cause of hospitilzations

A

acute vaso-occlusive crisis

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15
Q

Diagnosis of choice for sickle cell?

A

Hgb electrophoresis

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16
Q

Autoimmune suppression of hematopoiesis by a T cell mediated cellular mechanism

A

aplastic anemia

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17
Q

Basophillic stippling, target cells, poikilocytosis

A

Thalassemia

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18
Q

Lead line gum, foot drop, long bones lead lines

A

Sideroblastic Anemia

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19
Q

Elevated level of MMA and Homocysteine

A

B12

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20
Q

Risk factor for admin of Vit B12

A

Hypokalemia

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21
Q

Northern European and African American

A

Pernicious anemia

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22
Q

MC cause of folate acid deficiency?

A

inadequate dietary intake

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23
Q

RBC folic acid level?

A

<150 mg/ml

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24
Q

“Bite” or blister cells?

A

G6PD

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25
Q

Txt for G6PD?

A

self limited

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26
Q

Coombs test negative

A

Hereditary Spherocytosis

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27
Q

Disorder of RBC membrane, causing spherical shape

A

Hereditary Spherocytosis

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28
Q

Howell- Jolly bodies, and target cells (Hyposplenism)

A

Sickle cell Anemia

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29
Q

DOC for sickle cell?

A

Hgb electrophoresis

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30
Q

Panctyopenia

A

aplastic anemia

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31
Q

pallor, purpura, petechiae

A

aplastic anemia

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32
Q

TXT for aplastic anemia

A

supportive care

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33
Q

MC form of thrombocytopenia

A

immune thrombocytopenia

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34
Q

Hemorrhagic bullae

A

immune thrombocytopenia

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35
Q

Txt for immune thrombocytopenia?

A

corticosteriods

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36
Q

TTP defeiciency?

A

von Willebrand’s factor

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37
Q

Schistocytes, helmet cells

A

TTP

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38
Q

TXT for TTP?

A

Plasmapheresis

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39
Q

Hemolytic Uremic Syndrome bacteria?

A

E.coli

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40
Q

TXT for HUS?

A

supportive care

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41
Q

Decrease platelets and schistocytes?

42
Q

What does HELLP stand for?

A

Hemolysis, Elevated Liver enzymes, Low Platelets

43
Q

Severe form of DIC?

44
Q

Missing Factor 8

A

Hemophilia A

45
Q

Missing Factor 9

A

Hemophilia B

46
Q

Missing Factor 11

A

Hemophilia C

47
Q

Hemarthrosis?

A

Hemophilia A

48
Q

Ashkenzai Jewish descent?

A

Hemophilia C

49
Q

MC inherited bleeding disorder

A

Von Willebrand’s Disease

50
Q

MC von Willebrand type?

51
Q

TXT for von Willebrand?

52
Q

Des gamma carboxy prothrombin marker?

53
Q

Two factors the liver doesn’t produce?

A

VIII and vWF

54
Q

Deficiency in antithrombin III?

A

Antithrombin III

55
Q

Recurrent DVT and PE

A

Protein C and S deficiency

56
Q

MC of Protein C and S?

57
Q

Activated Protein C resistance test?

A

Factor V Leiden

58
Q

4 acquired hyper coagulability?

A

pregnancy
malignancy
OCP
Lupus anticoagulant

59
Q

Mutation in JAK2?

A

Polycythemia Vera

60
Q

Hemotocrit > 54% males, 51% females

A

Polycythemia Vera

61
Q

TXT for polycythemia vera?

A

Phlebotomy

62
Q

High altitudes?

A

Polycythemia vera

63
Q

Reed Sternberg cells

A

Hodgkin’s lymphoma

64
Q

Abdominal pain or fullness?

A

Non-Hodgkin’s lymphoma

65
Q

M-protein

A

Multiple Myeloma

66
Q

Lytic lesions, “Moth eaten”?

A

Multiple Myeloma

67
Q

Bence jones

A

Multiple Myeloma

68
Q

Rouleaux formation and hypercalcemia

A

Multiple Myeloma

69
Q

TXT for multiple myeloma?

A

biologic agents (IMIDs) and Dexmethasone

70
Q

Most common childhood malignancy?

A

Acute Lymphoblastic Leukemia

71
Q

Philadelphia chromosome w/ poor prognosis?

72
Q

negative peroxidase and sudan black stain

A

acute lymphoblastic leukemia

73
Q

MC form of leukemia in adults in US

A

Chronic lymphoblastic leukemia

74
Q

Proliferation of MATURE lymphocytes in peripheral

75
Q

Smudge cells?

A

Chronic Lymphoblastic leukemia (CLL)

76
Q

Lymphocytosis?

77
Q

Auer rods?

A

Acute myeloid leukemia (AML)

78
Q

Peroxidase and sudan black stain posItive

A

acute myeloid leukemia (AML)

79
Q

Philadelphia chromosome

A

chronic myeloid leukemia (CML)

80
Q

TXT for CML?

A

Tyrosine kinase inhibitor (Imatnib)

81
Q

Dx for chronic myeloid leukemia?

82
Q

MC type of Hodgkin?

83
Q

Staging of Lymphomas?

A

Stage I- 1 lymph node region involved
Stage II- 2 or more lymph node regions involved, one side of diaphragm
Stage III- lymph nodes regions on both sides of diaphragm
Stage IV- disseminated w/ extra nodal involvement

84
Q

Difference between folic and B12 defiecincy

A

neuro abnormalities

85
Q

How do you distinguish between hemolytic anemia’s?

A

Coombs test

Hgb Electrophoresis

86
Q

TXT for chronic anemia?

A

Darbepoetin, Erythropoietin

87
Q

List four disease states in which you may find

basophilic stippling

A

Lead poisoning, beta or alpha thalassemia, sideroblastic anemia,

88
Q

What molecule binds iron in the blood stream?

A

Transferrin

89
Q

Inability to absorb vitamin B12 due to lack of

intrinsic factor is what disease?

A

Perinicous anemia

90
Q

Will unconjugated bilirubin be high or low in a

patient with sickle cell disease?

91
Q

Would anemia of chronic disease most likely be

macrocytic, normocytic or microcytic?

A

normocytic

92
Q

Will the serum ferritin be high or low in a patient

with iron deficient anemia?

A

It will almost always be low

93
Q

G6PD deficiency follows what pattern of

inheritance?

94
Q

Strict vegans are at risk for what type of anemia?

A

B12 deficiency anemia

95
Q

The term Philadelphia chromosome should make

you think of what diagnosis?

A

Chronic myeloid leukemia

96
Q

List the three diagnosis you should be thinking of if

a question includes Heinz bodies.

A

G6PD deficiency anemia, chronic liver

disease, alpha thalassemia

97
Q

Normal range for MCV?

98
Q

Are target cells seen in mild or severe iron

deficiency anemia?

99
Q

How do you treat a sickle cell crisis?

A

Fluids, oxygen, pain medication,

transfusion may be necessary

100
Q

A patient of Mediterranean descent is a clue for

which type of anemia?

A

Beta thalassemia