Hematology ASCP Review UPDATED ACTUAL Questions and
CORRECT Answers
1. Alkaline Electrophoresis pattern C, S. F, A
2. Acid Electrophoresis pattern F, A, S, C
3. T cell Markers CD2, CD3, CD4, CD8
4. B cell markers CD19, CD20
5. WBC common marker CD45
6. Stem Cell marker CD34
7. Assay for heparin aPTT
8. Warfarin Assay PT/INR
9. MCV (Hct/RBC) x 10
10. MCH (Hgb/RBC) x 10
11. MCHC Hgb/Hct x 100
12. Fetal Hemoglobin Chains Alpha and gamma
13. A2 Hemoglobin chains Alpha and delta
14. Multiple Myeloma IgG, Bone lesions, rouleaux, plasma cells
15. Waldenstroms Macroglobulinemia IgM, High blood viscosity
16. CSF WBC Lymphs mostly, some monos
17. Prussian blue stain Iron
18. What happens to sickle cells upon re- They return to normal
oxygenation?
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, Hematology ASCP Review UPDATED ACTUAL Questions and
CORRECT Answers
19. Hemoglobin H chains Four Beta chains
20. May hegllin anomalies can be con- Giant Platelets
firmed by the presence of?
21. Heinz bodies can be viewed only with Supravital stein, caused by G6PD deficiency
22. Primary site of clotting factors Liver
23. Type of hemoglobin measured in Cyanomethemoglobin
HgB determinations?
24. Low molecular weight heparin assay anti-XA
25. Normal LAP score 20-100, low=CML, high=Leukamoid+PV
26. Platelet satalitism is caused by? EDTA
27. Alpha thalassemia silent carrier 1/4 genes mutated, no clinical signs, Chromosome
16
28. Alpha thalassemia minor 2/4 genes mutated, decreased hemoglobin and
mild anemia, some hemoglobin barts, Chromo-
some 16
29. Alpha thalassemia intermedia 3/4 genes mutated, Hemoglobin H disease, Chro-
mosome 16
30. Alpha thalassemia major 4/4 genes mutated, Hydrops fatalis, death, 80%
hemoglobin barts, Chromosome 16
31. Beta thalassemia minor 1/2 beta chains defect, mild anemia, Chromosome
11
2/9
CORRECT Answers
1. Alkaline Electrophoresis pattern C, S. F, A
2. Acid Electrophoresis pattern F, A, S, C
3. T cell Markers CD2, CD3, CD4, CD8
4. B cell markers CD19, CD20
5. WBC common marker CD45
6. Stem Cell marker CD34
7. Assay for heparin aPTT
8. Warfarin Assay PT/INR
9. MCV (Hct/RBC) x 10
10. MCH (Hgb/RBC) x 10
11. MCHC Hgb/Hct x 100
12. Fetal Hemoglobin Chains Alpha and gamma
13. A2 Hemoglobin chains Alpha and delta
14. Multiple Myeloma IgG, Bone lesions, rouleaux, plasma cells
15. Waldenstroms Macroglobulinemia IgM, High blood viscosity
16. CSF WBC Lymphs mostly, some monos
17. Prussian blue stain Iron
18. What happens to sickle cells upon re- They return to normal
oxygenation?
1/9
, Hematology ASCP Review UPDATED ACTUAL Questions and
CORRECT Answers
19. Hemoglobin H chains Four Beta chains
20. May hegllin anomalies can be con- Giant Platelets
firmed by the presence of?
21. Heinz bodies can be viewed only with Supravital stein, caused by G6PD deficiency
22. Primary site of clotting factors Liver
23. Type of hemoglobin measured in Cyanomethemoglobin
HgB determinations?
24. Low molecular weight heparin assay anti-XA
25. Normal LAP score 20-100, low=CML, high=Leukamoid+PV
26. Platelet satalitism is caused by? EDTA
27. Alpha thalassemia silent carrier 1/4 genes mutated, no clinical signs, Chromosome
16
28. Alpha thalassemia minor 2/4 genes mutated, decreased hemoglobin and
mild anemia, some hemoglobin barts, Chromo-
some 16
29. Alpha thalassemia intermedia 3/4 genes mutated, Hemoglobin H disease, Chro-
mosome 16
30. Alpha thalassemia major 4/4 genes mutated, Hydrops fatalis, death, 80%
hemoglobin barts, Chromosome 16
31. Beta thalassemia minor 1/2 beta chains defect, mild anemia, Chromosome
11
2/9
