Hemolytic Anemias

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1.
FLASHCARD QUESTION
Front
These inclusions which cannot be visualized on Wright-stained peripheral smears are often associated with:
Back
G6PD deficiency
2.
FLASHCARD QUESTION
Front
Which RBC morphology is formed as a result of Heinz bodies being pitted from the RBC in the spleen? Options: acanthocytes, burr cells, stomatocytes
Back
bite cells
3.
FLASHCARD QUESTION
Front
Which hemolytic disorder has RBCs that are especially sensitive to lysis by complement? Options: PNH, PCH, Hereditary spherocytosis, G6PD deficiency
Back
PNH
4.
FLASHCARD QUESTION
Front
An anemia that manifests as decreased marrow cellularity, cytopenias in two cellular elements, and reticulocytopenia is termed
Back
Aplastic anemia
5.
FLASHCARD QUESTION
Front
Individuals with Fanconi's anemia characteristically show
Back
Increased Hgb F
6.
FLASHCARD QUESTION
Front
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
Back
MCV - 80.5, MCH - 33.4, MCHC - 39.0
7.
FLASHCARD QUESTION
Front
Choose the principal confirmation test for a diagnosis of hereditary spherocytosis: autohemolysis test, sucrose hemolysis test, thermal stability test, osmotic fragility test
Back
osmotic fragility test
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