Hemolytic Anemias

Hemolytic Anemias

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University

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18 questions

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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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