Haematology Practice Exam
Prepare effectively for your ASCP and MLT certification with our Hematology Practice Exams. These exams are tailored to cover key topics such as red and white blood cell abnormalities, anemia classifications, coagulation pathways, and hematologic malignancies. Each question is designed to match ASCP exam standards and includes clear explanations to help you master the material and boost your test-taking confidence.
1. Which red blood cell indices are most useful in distinguishing microcytic anaemias?
A) MCV
B) MCH
C) MCHC
D) RDW
2. Heinz bodies are composed of which of the following?
A) DNA
B) Iron
C) Denatured haemoglobin
D) RNA
3. What is the most probable cause of a decreased ESR (erythrocyte sedimentation rate)?
A) Inflammation
B) High fibrinogen
C) Sickle cell anaemia
D) Pregnancy
4. Which inclusion is typically seen in lead poisoning?
A) Howell-Jolly bodies
B) Heinz bodies
C) Pappenheimer bodies
D) Basophilic stippling
5. What is the most appropriate stain for detecting iron in bone marrow?
A) Wright-Giemsa
B) Sudan black B
C) Prussian blue
D) PAS
6. Which of the following cells is the earliest recognizable erythroid precursor?
A) Reticulocyte
B) Pronormoblast
C) Basophilic normoblast
D) Orthochromatic normoblast
7. The LAP (leukocyte alkaline phosphatase) score is typically elevated in:
A) Chronic myelogenous leukaemia (CML)
B) Leukemoid reaction
C) Acute lymphoblastic leukaemia (ALL)
D) Aplastic anemia
8. A patient with chronic lymphocytic leukemia (CLL) would likely have which of the following findings?
A) Increased blasts
B) Hypersegmented neutrophils
C) Smudge cells
D) Döhle bodies
9. The most common cause of hereditary spherocytosis is a defect in which protein?
A) Haemoglobin
B) Spectrin
C) Fibrinogen
D) Actin
10. Which of the following is the most appropriate test to confirm a suspected diagnosis of PNH (Paroxysmal Nocturnal Hemoglobinuria)?
A) Coombs test
B) Flow cytometry for CD55/CD59
C) Osmotic fragility test
D) Haemoglobin electrophoresis
11. Which of the following findings is most consistent with megaloblastic anemia?
A) Target cells
B) Microcytic hypochromic cells
C) Oval macrocytes and hypersegmented neutrophils
D) Spherocytes
12. In iron deficiency anaemia, the TIBC is typically:
A) Decreased
B) Increased
C) Normal
D) Variable
13. Which of the following is a characteristic finding in chronic myelogenous leukemia (CML)?
A) Auer rods
B) Philadelphia chromosome
C) Increased LAP score
D) Smudge cells
14. Which RBC abnormality is associated with G6PD deficiency following oxidative stress?
A) Target cells
B) Spherocytes
C) Bite cells
D) Elliptocytes
15. What is the key feature of polycythemia vera?
A) Decreased RBC mass
B) JAK2 mutation
C) Elevated erythropoietin
D) Bone marrow failure
16. The presence of Auer rods in blasts is indicative of:
A) ALL
B) AML
C) CLL
D) CML
17. Which test is used to monitor heparin therapy?
A) PT
B) INR
C) aPTT
D) Bleeding time
18. The Philadelphia chromosome results from a translocation between chromosomes:
A) 9 and 22
B) 8 and 14
C) 15 and 17
D) 11 and 22
19. What is the expected bone marrow finding in aplastic anemia?
A) Hypercellularity
B) Increased megakaryocytes
C) Hypocellularity
D) Increased blasts
20. Rouleaux formation is most commonly seen in:
A) Hereditary spherocytosis
B) Iron deficiency anemia
C) Multiple myeloma
D) Sickle cell disease
21. Which stain is used to differentiate myeloblasts from lymphoblasts?
A) PAS
B) Prussian blue
C) Myeloperoxidase (MPO)
D) Wright-Giemsa
22. The M:E ratio in normal bone marrow is typically around:
A) 1:1
B) 2:1 to 4:1
C) 5:1
D) 10:1
23. In which conditions would schistocytes most likely be found?
A) Iron deficiency anaemia
B) Thalassemia
C) DIC
D) Aplastic anemia
24. In hereditary elliptocytosis, the predominant RBC shape is:
A) Sickle-shaped
B) Round
C) Elliptical
D) Tear-drop
25. The reticulocyte count is typically increased in which of the following?
A) Aplastic anaemia
B) Hemolytic anaemia
C) Iron deficiency anaemia
D) Thalassemia trait
26. Which form of hemoglobin occurs naturally in circulation and contributes to normal oxygen delivery?
A. Methemoglobin
B. Deoxyhemoglobin
C. Carboxyhemoglobin
D. Sulfhemoglobin
27. What condition typically causes a right shift in the oxyhemoglobin dissociation curve, promoting oxygen release to tissues?
A. Alkalosis
B. Massive transfusion
C. Acidosis
D. Presence of fetal hemoglobin
28. In a patient with aplastic anemia, which white cell type is most commonly seen on peripheral blood smear?
A. Lymphocytes
B. Neutrophils
C. Monocytes
D. Eosinophils
29. What is the normal range for lymphocytes in an adult WBC differential?
A. 10–20%
B. 5–10%
C. 50–70%
D. 20–44%
30. A 4-year-old child presents with 60% lymphocytes on a CBC. What is the correct interpretation?
A. Leukemia
B. Normal finding for this age group
C. Lymphopenia
D. Viral infection
31. Which automated differential result should prompt a manual smear review?
A. Monocytes = 15%
B. Bands = 6%
C. Segmented neutrophils = 70%
D. Eosinophils = 2%
32. At which erythroid maturation stage does hemoglobin production cause cytoplasm to begin turning pink?
A. Reticulocyte
B. Pronormoblast
C. Polychromatic normoblast
D. Basophilic normoblast
33. Which condition does NOT cause a rightward shift in the hemoglobin oxygen dissociation curve?
A. Alkalosis
B. Acidosis
C. Fever
D. Increased 2,3-DPG
34. What hemoglobin variant consists of four beta chains and is found in Hemoglobin H disease?
A. Hb H (β₄)
B. Hb F (γ₄)
C. Hb A2 (α₂δ₂)
D. Hb A (α₂β₂)
35. What lab abnormalities are caused by red cell autoagglutination at room temperature?
A. Increased hematocrit
B. Decreased MCV
C. Normal RBC count
D. Low RBC count with falsely high MCV
36. What is the most typical blood cell pattern in hypersplenism?
A. Pancytosis
B. Cytopenias with splenomegaly
C. Leukemoid reaction
D. Polycythemia
37. Which organ removes inclusions from red blood cells through a process called “pitting”?
A. Liver
B. Bone marrow
C. Spleen
D. Kidneys
38. Which of the following is NOT characteristic of spherocytes?
A. Reduced surface area
B. Lack of central pallor
C. Poor osmotic tolerance
D. Increased deformability
39. Which form of hemolysis is more typical in hereditary spherocytosis?
A. Intravascular
B. Complement-mediated
C. Extravascular
D. Mechanical trauma-related
40. In which disorder is osmotic fragility increased?
A. Hereditary elliptocytosis
B. Hereditary spherocytosis
C. Iron deficiency anemia
D. Thalassemia minor
41. Sickle cell anemia is best categorized as what type of anemia based on red cell indices?
A. Normocytic, normochromic
B. Microcytic, hypochromic
C. Normocytic, hypochromic
D. Macrocytic, normochromic
42. What is the major hemoglobin component in individuals with sickle cell trait?
A. Hemoglobin F
B. Hemoglobin C
C. Hemoglobin S
D. Hemoglobin A
43. What genetic mutation causes sickle cell disease?
A. Valine replaces glutamic acid at position 6 of the β-globin chain
B. Lysine replaces glutamic acid in α-globin
C. Aspartate replaces lysine in β-globin
D. Valine replaces histidine in α-globin
44. Hemoglobin C disease is characterized by all of the following EXCEPT:
A. Target cells
B. Hemoglobin C crystals
C. Lysine-for-glutamic acid substitution
D. Fast migration on alkaline electrophoresis
45. Which hemoglobins migrate with Hb A2 on alkaline electrophoresis?
A. Hemoglobin S
B. Hemoglobin H
C. Hemoglobin F
D. Hemoglobin C
46. Which of the following electrophoresis results is consistent with sickle cell trait?
A. Hb A = 40%, Hb S = 35%, Hb F = 5%
B. Hb A = 0%, Hb F = 95%, Hb A2 = 5%
C. Hb A = 60%, Hb S = 40%, Hb A2 = 2%
D. Hb A = 80%, Hb S = 10%, Hb A2 = 10%
47. Which condition commonly leads to autosplenectomy due to repeated splenic infarction?
A. Sickle cell disease
B. Thalassemia major
C. Hemoglobin C disease
D. Hereditary spherocytosis
48. Paroxysmal nocturnal hemoglobinuria (PNH) is best described as:
A. A hereditary red cell enzyme defect
B. An acquired stem cell disorder with complement sensitivity
C. An autosomal recessive trait
D. A congenital RBC membrane disorder
49. Which antibody is implicated in paroxysmal cold hemoglobinuria (PCH)?
A. Anti-i
B. Anti-P
C. Anti-M
D. Anti-I
50. Which feature is NOT typical of intravascular hemolysis?
A. Hemoglobinemia
B. Hemoglobinuria
C. Methemoglobinemia
D. Decreased haptoglobin
