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Clinical Laboratory Science Solved Exam Questions - 414 Verified Questions

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Clinical Laboratory Science

Solved Exam Questions

Course Introduction

Clinical Laboratory Science is an interdisciplinary course that introduces students to the theoretical principles and practical applications of laboratory testing in the diagnosis, treatment, and prevention of disease. The course covers key areas such as hematology, clinical chemistry, microbiology, immunology, and molecular diagnostics, emphasizing the role of laboratory professionals in supporting patient care through accurate and timely analysis of biological samples. Students gain proficiency in standard laboratory techniques, quality assurance, and the interpretation of test results, along with an understanding of laboratory safety, ethics, and regulatory requirements.

Recommended Textbook

Hematology in Practice 2nd Edition by Betty Ciesla

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19 Chapters

414 Verified Questions

414 Flashcards

Source URL: https://quizplus.com/study-set/3886 Page 2

Chapter 1: Introduction to Hematology and Basic Laboratory Practice

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20 Verified Questions

20 Flashcards

Source URL: https://quizplus.com/quiz/77408

Sample Questions

Q1) Proper mixing of samples and timely delivery of samples to the laboratory are both examples of:

A) Delta checks

B) Postanalytic variables

C) Preanalytic variables

D) Reflex testing

Answer: C

Q2) Which of the following is the definition of a reference interval?

A) A solution of a known amount of analyte

B) Materials analyzed concurrently with unknown samples

C) Values established for a particular analyte, given a method, instrument, or patient population

D) Validation techniques on flagged samples

Answer: C

Q3) Standards and calibrators differ from control materials because:

A) An exact amount of analyte is present in a standard or calibrator

B) A variable amount of analyte is present depending on patient samples

C) Standards only need to be within a target range

D) Standards are run to the best estimate of the known value

Answer: A

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Chapter 2: From Hematopoiesis to the Complete Blood Count

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20 Verified Questions

20 Flashcards

Source URL: https://quizplus.com/quiz/77407

Sample Questions

Q1) Opsonizing antibodies produced by the spleen serve to:

A) Strip the capsule from bacterial pathogens

B) Recycle erythrocyte byproducts

C) Aid in extramedullary hematopoiesis

D) Fight viral infection

Answer: A

Q2) A patient's hemoglobin is 12.3 g/dL.On the peripheral smear, the red cells appear normochromic, normocytic.The hematocrit value that correlates with these data is:

A) 34%

B) 37%

C) 40%

D) 43%

Answer: B

Q3) Bone marrow aspiration is usually required in conditions of:

A) Anemia

B) Hypoxia

C) Leukemia

D) Hepatosplenomegaly

Answer: C

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Chapter 3: Red Blood Cell Production, Function, and

Relevant Red Blood Cell Morphology

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24 Verified Questions

24 Flashcards

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Sample Questions

Q1) Most hypochromic cells will have an MCHC that is:

A) Greater than 36%

B) Less than 30%

C) Greater than 27%

D) Less than 27%

Answer: B

Q2) The anucleate mature red blood cell has no ability to produce protein.

A)True

B)False

Answer: True

Q3) The last nucleated stage of erythrocytic maturation is the:

A) Pronormoblast

B) Orthochromic normoblast

C) Polychromatophilic normoblast

D) Basophilic normoblast

Answer: B

Q4) The higher the N:C ratio, the more mature the cell.

A)True

B)False

Answer: False

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Chapter 4: Hemoglobin Function and Principles of Hemolysis

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20 Verified Questions

20 Flashcards

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Sample Questions

Q1) Which of the following clinical conditions is a definitive sign of intravascular lysis?

A) Bilirubinemia

B) Decreased RBC count

C) Hemoglobinuria

D) Elevated LDH

Q2) Hemoglobin begins to be synthesized at the polychromatophilic stage of red cell development.

A)True

B)False

Q3) Abnormal hemoglobins have a lower affinity for oxygen.

A)True

B)False

Q4) Which of the following abnormal hemoglobins will result in a cyanotic condition?

A) Sulfhemoglobin

B) Cyanmethemoglobin

C) Hemoglobin F

D) Hemoglobin M

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Chapter 5: The Microcytic Anemias

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26 Verified Questions

26 Flashcards

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Sample Questions

Q1) The alpha thalassemias result from:

A) Gene deletion

B) Defective alpha genes

C) Iron overload

D) Excessive production of alpha chains

Q2) What is the presumptive clinical condition?

A) Pernicious anemia

B) Autoimmune hemolytic anemia

C) Iron deficiency trait

D) Thalassemia trait

Q3) A 15-year-old Lebanese boy was sent to the laboratory for an evaluation of anemia and had the following lab results:

A) WBC = 7.5 \(\times\) 10<sup>9</sup>/L

B) RBC = 5.9 \(\times\) 10<sup>12</sup>/L

C) Hgb = 11.6 g/dL

D) Hct = 36%

Q4) In regards to the thalassemias, the deficit has nothing to do with iron.

A)True

B)False

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Chapter 6: The Macrocytic Anemias

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17 Verified Questions

17 Flashcards

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Sample Questions

Q1) One of the most common pathophysiologies that contribute to folic acid deficiency is:

A) Tropical sprue

B) Intrinsic factor deficiency

C) IDA

D) Infection with Diphyllobothrium latum

Q2) Which of the following terms describes the appearance of the erythropoietic precursors in the megaloblastic process?

A) Ordered arrangement of chromatin

B) Asynchrony

C) Eccentric nucleus

D) Pale cytoplasm

Q3) A bone marrow aspiration/examination is not necessary for patients with megaloblastic anemia.

A)True

B)False

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8

Chapter 7: Normochromic Anemias: Biochemical,

Membrane, and Miscellaneous Red Blood Cell Disorders

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20 Verified Questions

20 Flashcards

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Sample Questions

Q1) The inclusions pictured below are seen with supravital staining only.These inclusions are most likely:

A) Heinz bodies

B) Howell-Jolly bodies

C) Pappenheimer bodies

D) Due to stain contamination

Q2) Individuals with Fanconi's anemia characteristically will have:

A) Intravascular hemolysis

B) Increased Hgb F

C) Ringed sideroblastics

D) Thrombocytosis

Q3) In hereditary spherocytosis, the reticulocyte count will typically be:

A) Less than 0.5%

B) 0.5% to 1.5%

C) 3% to 10%

D) Greater than 10%

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9

Chapter 8: The Normochromic Anemias Caused by

Hemoglobinopathies

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23 Verified Questions

23 Flashcards

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Sample Questions

Q1) In sickle cell anemia, _____is substituted for glutamine.

A) valine

B) lysine

C) adenine

D) leucine

Q2) In hemoglobin C disease, is substituted for glutamic acid.

A) valine

B) adenine

C) lysine

D) leucine

Q3) A blood smear from a patient with sickle cell crisis shows 80 nucleated red cells per 100 leukocytes.The total leukocyte count is 18 \(\times\) 10<sup>9</sup>/L.The corrected white cell count is:

A) 17,200

B) 9,000

C) 10,000

D) 13,400

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Page 10

Chapter 9: Leukopoiesis and Leukopoietic Function

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20 Verified Questions

20 Flashcards

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Sample Questions

Q1) In automated hematology, what is the definition of the delta check?

A) Spinning the sample for hematocrit value

B) Comparison to previous value

C) Flagging criteria

D) Performing a manual platelet count

Q2) There are ___ maturation stages in the neutrophil.

A) five

B) four

C) three

D) six

Q3) Lymphocyte concentrations in peripheral blood are greatest during what age interval?

A) Immediately after birth

B) Older adult (40 to 70 years)

C) Young adult (16 to 40 years)

D) Young child (1 to 4 years)

Q4) The absolute WBC count refers to the percentage of a particular cell counted from the 100 WBC differential.

A)True

B)False

Page 11

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Chapter 10: Abnormalities of White Blood Cells:

Quantitative, Qualitative, and the Lipid Storage Diseases

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20 Verified Questions

20 Flashcards

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Sample Questions

Q1) All of the following are lipid storage syndromes/diseases except:

A) Gaucher's disease

B) Tay-Sachs disease

C) Chediak-Higashi syndrome

D) Niemann-Pick disease

Q2) Pelger-Huët anomaly is characterized mainly by:

A) Neutrophils with gray-green granules

B) Lipid depositions in the cytoplasm

C) Giant platelets

D) Hyposegmentation of the nucleus in the neutrophils

Q3) Infectious mononucleosis is caused by the EBV virus, which infects B lymphocytes.

A)True

B)False

Q4) Toxic granulation in neutrophils is a direct result of:

A) Cytokine production

B) Enhanced lysosome enzyme production

C) Toxic granulation

D) Ehrlichia infection

Page 12

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Chapter 11: Acute Leukemias

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25 Verified Questions

25 Flashcards

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Sample Questions

Q1) A patient presents with generalized lymphadenopathy and a WBC of 100 \(\times\) 10<sup>9</sup>/L.This hematologic picture would most likely be seen in:

A) Chronic lymphocytic leukemia

B) Acute lymphocytic leukemia

C) Burkitt's lymphoma

D) Hairy cell leukemia

Q2) Pure erythroid leukemia is defined as:

A) Erythroid precursors greater than 30%, myeloblasts less than 20%

B) Erythroid precursors greater than 50%, myeloblasts less than 40%

C) Erythroid precursors less than 50%

D) Erythroid precursors greater than 80%

Q3) Which of the following is characteristic of Auer rods?

A) Composed of fused primary granules

B) Predominantly seen in ALL

C) Predominantly seen in HCL

D) Composed of specific granules

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Chapter 12: Chronic Myeloproliferative Disorders

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24 Verified Questions

24 Flashcards

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Sample Questions

Q1) All of the following are causes of secondary erythrocytosis except:

A) Hypertension

B) Alcohol

C) Sleep apnea

D) Smoking

Q2) Plethora is a condition associated with:

A) Polycythemia vera

B) CML

C) Leukemoid reaction

D) Myelofibrosis

Q3) The JAK2 chromosomal mutation is associated with:

A) Polycythemia vera

B) CML

C) Leukemoid reaction

D) Myelofibrosis

Q4) What is the pathophysiology of the myeloproliferative disorders?

A) Fibroid infiltration of major organs

B) Neoplastic transformation of multipotential stem cells

C) Widespread deterioration of cellular function

D) Splenic sequestration of normal blood cells

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Chapter 13: Lymphoproliferative Disorders and Related

Plasma Cell Disorders

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20 Verified Questions

20 Flashcards

Source URL: https://quizplus.com/quiz/77396

Sample Questions

Q1) A significant feature of hairy cell leukemia not seen is other acute leukemias is:

A) Panmyelosis

B) Pancytosis

C) Pancytopenia

D) Panhyperplasia

Q2) The most characteristic change seen in the peripheral smear of a patient with multiple myeloma is the presence of:

A) Microcytic hypochromic cells

B) Intracellular inclusion bodies

C) Rouleaux

D) Agglutination

Q3) Hypogammaglobulinemia is a significant feature in half of patients with CLL.This complication can lead to:

A) Refractory anemia

B) Essential thrombocytosis

C) Autoimmune hemolytic anemia

D) Pernicious anemia

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Page 15

Chapter 14: The Myelodysplastic Syndromes

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20 Verified Questions

20 Flashcards

Source URL: https://quizplus.com/quiz/77395

Sample Questions

Q1) All of the following are associated with the development of the MDSs except:

A) Alkylating therapy

B) Benzene exposure

C) Alcoholism

D) Radiation

Q2) The FAB classification of the MDSs include CML.

A)True

B)False

Q3) Refractory anemia is an anemia that:

A) Has more than 5% blasts in the peripheral blood

B) Is resistant to treatment

C) Will usually demonstrate a hypoplastic bone marrow

D) Demonstrates a 17g deletion routinely

Q4) All of the following are dysplastic changes of platelets frequently seen in MDS except:

A) Abnormal granulation

B) Micromega karyocytes

C) Giant platelets

D) Platelet satellitism

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Chapter 15: Overview of Hemostasis and Platelet Physiology

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30 Verified Questions

30 Flashcards

Source URL: https://quizplus.com/quiz/77394

Sample Questions

Q1) Tissue factor pathway inhibitor (TFPI):

A) Prevents activation of factor X by VIIa

B) Activates the common pathway

C) Inhibits fibrinolysis

D) Inhibits the kallikrein proteins

Q2) The prothrombin group of factors consists of factors:

A) I, V, VIII, and XIII

B) XI, XII, prekallikrein, and HMWK

C) II, VII, IX, and X

D) III, VIII, IX, and X

Q3) Factor III

A)Stabile factor

B)Labile factor

C)Thromboplastin

D)Calcium

E)Anti-hemophiliac factor

F)Fibrinogen

G)Prothrombin

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17

Chapter 16: Quantitative and Qualitative Platelet Disorders

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25 Verified Questions

25 Flashcards

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Sample Questions

Q1) The correct anticoagulant-to-blood ratio for coagulation samples is:

A) 4:1

B) 9:1

C) 1:9

D) 1:4

Q2) The presence of thrombocytopenia and giant platelets on the peripheral smear of a patient is characteristic of:

A) Classic von Willebrand's disease

B) Hemophilia A

C) Glanzmann's thrombasthenia

D) Bernard-Soulier syndrome

Q3) In thrombotic thrombocytopenic purpura, which of the following statements is the most accurate?

A) It is associated with E. coli O157:H7.

B) It is associated with fever, renal failure, and neurological complications.

C) The organ most affected is the kidney.

D) More males are affected than females

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18

Chapter 17: Defects of Plasma Clotting Factors

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20 Verified Questions

20 Flashcards

Source URL: https://quizplus.com/quiz/77392

Sample Questions

Q1) A prolonged aPTT is corrected with factor VIII-deficient plasma but not with factor IX-deficient plasma.What factor is deficient?

A) IX

B) XIII

C) V

D) X

Q2) Which result will be within reference range in a patient with dysfibrinogenemia?

A) Thrombin time

B) Activated partial thromboplastin time

C) Immunologic fibrinogen level

D) Protein electrophoresis

Q3) Which of the following is the most prevalent inherited bleeding disorder?

A) von Willebrand disease

B) Hemophilia A

C) Factor VII deficiency

D) Factor XII deficiency

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Chapter 18: Fibrinogen, Thrombin, and the Fibrinolytic System

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20 Flashcards

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Sample Questions

Q1) The best component to use for patients with afibrinogenemia is:

A) Whole blood

B) Fresh frozen plasma

C) Tissue plasminogen activator

D) Factor XIII

Q2) An excess of which of the following is indicative of the breakdown of fibrin products within the circulating blood?

A) D-dimers

B) Alpha-2-antiplasmin

C) Protein C

D) Plasmin

Q3) The reference range for a thrombin time is:

A) 20 to 40 seconds

B) 100 to 120 seconds

C) 40 to 60 seconds

D) 11 to 15 seconds

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Chapter 19: Introduction to Thrombosis and Anticoagulant Therapy

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20 Verified Questions

20 Flashcards

Source URL: https://quizplus.com/quiz/77390

Sample Questions

Q1) The most common tests used to detect Lupus anticoagulants include all of the following except:

A) aPTT

B) Kaolin clotting time

C) PT/INR

D) Dilute Russell viper venom test

Q2) Heparin:

A) Inhibits PF3

B) Inhibits thrombin

C) Degrades antithrombin

D) Complexes with protein C

Q3) Coumadin acts in such a way that it:

A) Alters the synthesis of vitamin K-dependent factors

B) Reduces the circulating level of factors III and V

C) Reduces the circulating level of factor I

D) Cleaves carboxyreductase to generate glutamic acid

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