
Hemolytic Anemias
Authored by Sheryl Schloss
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University
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20 questions
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1.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
These inclusions which cannot be visualized on Wright-stained peripheral smears are often associated with:
Pyruvate kinase deficiency
Basophilic stippling
Hgb H inclusion bodies
G6PD
deficiency
2.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
Which RBC morphology is formed as a result of Heinz bodies being pitted from the RBC in the spleen
acanthocytes
bite cells
burr cells
stomatocytes
3.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
Which of the following hemolytic disorders has RBCs that are especially sensitive to lysis by complement
PNH
PCH
Hereditary spherocytosis
G6PD deficiency
4.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
An anemia that manifests as decreased marrow cellularity, cytopenias in two cellular elements, and reticulocytopenia is termed
Diamond Blackfan Anemia
Aplastic anemia
Sideroblastic anemia
Hemolytic anemia
5.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
Individuals with Fanconi's anemia characteristically show
intravascular hemolysis
Increased Hgb F
Ringed Sideroblasts
Increased Hgb H
6.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
Which of the following red cell indices would most likely be found in Hereditary spherocytosis?
MCV - 87
MCH - 29.9
MCHC- 34.5
MCV - 65
MCH - 27
MCHC - 29.8
MCV - 80.5
MCH - 33.4
MCHC - 39.0
MCV 101
MCH 30
MCHC - 33.0
7.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
Choose the principal confirmation test for a diagnosis of hereditary spherocytosis
autohemolysis test
sucrose hemolysis test
thermal stability test
osmotic fragility test
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