MediaLab Hematology Practice Questions Part 1

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Last updated 5:43 PM on 8/26/26
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140 Terms

1
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Detecting the BCR/ABL1 mutation by molecular techniques is useful in the diagnosis of which of the following diseases/conditions?

A) Paroxysmal Nocturnal Hemoglobinuria (PNH)

B) Chronic myelogenous leukemia (CML)

C) Acute Promyelocytic Leukemia (APL)

D) Iron Deficiency Anemia (IDA)

Chronic myelogenous leukemia (CML)

2
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What is a common early laboratory marker of hereditary hemochromatosis (HH)?

A) Increased serum ferritin

B) Decreased serum iron

C) Decreased transferrin saturation

D) Increased hemoglobin

Increased serum ferritin

3
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What is the predominant abnormal erythrocyte morphology associated with idiopathic myelofibrosis?

A) Target cells

B) Elliptocytes

C) Teardrop cells

D) Ovalocytes

Teardrop cells

4
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A hemoglobin F concentration of 100% may be seen in which beta thalassemia?

A) Beta thalassemia minor (ß0/ß)

B) Beta thalassemia major (ß0/ß0)

C) Delta-beta thalassemia minor (dß0/ß)

D) Delta-beta thalassemia major (dß0/dß0)

Delta-beta thalassemia major (dß0/dß0)

5
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Which of the following conditions would produce the results listed below in an anemic patient?

MCV = 115 fL

MCH = 30 pg

MCHC = 34 %

A) Sickle cell anemia

B) Aplastic anemia

C) Iron deficiency anemia

D) Pernicious anemia

Pernicious anemia

6
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Which abnormal gene is inherited with Chediak-Higashi syndrome resulting in dysfunctional cells causing greater susceptibility to infections?

A) CHS1 LYST

B) JAK2

C) TET2

D) ADAMTS13

CHS1 LYST

7
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What is the composition of the granules associated with basophilic stippling?

A) Aggregates of iron

B) Aggregates of hemoglobin

C) Aggregates of ribosomes

D) Aggregates of DNA

Aggregates of ribosomes

8
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A 1:100 dilution of a patient's peripheral blood was made, and a total of 136 platelets were counted in 5 squares of the RBC area of a Neubauer-ruled hemocytometer. What is the Platelet count? Note: The volume correction factor is 50 µL.

A) 27 x 103/µL

B) 68 x 103/µL

C) 136 x 103/µL

D) 680 x 103/µL

680 x 103/µL

9
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A cerebrospinal fluid sample was taken from an inpatient with severe neurological symptoms. The image shows a field from a cytospin preparation from this patient's fluid. What findings are present in this field?

A) Blast cells

B) Mesothelial cells

C) Choroid plexus clump

D) Tumor cells

Tumor cells

10
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What principle(s) of flow cytometry is employed when performing immuno-phenotyping?

A) Diffraction grating

B) Impedance

C) Diffraction grating and impedance

D) Fluorescent antibody tagging and light scatter

Fluorescent antibody tagging and light scatter

11
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What are the smallest nucleated cells seen in normal peripheral blood?

A) Lymphocytes

B) Segmented neutrophils

C) Monocytes

D) Platelets

Lymphocytes

12
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Esterase stains are used to help differentiate which of the following?

A) Myeloblasts from lymphoblasts

B) Monoblasts from myeloblasts

C) Monoblasts from lymphoblasts

D) Erythroblasts from lymphoblasts

Monoblasts from myeloblasts

13
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What is the most significant cause of decreased haptoglobin levels?

A) Acute infection

B) Intravascular hemolysis

C) Liver disease

D) Myoglobinuria

Intravascular hemolysis

14
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The large blue staining cells represented in the photomicrographs comprise 50% of the total white blood cell count. Which of the following conditions is this peripheral blood picture most consistent with?

A) Infectious mononucleosis

B) Chronic lymphocytic leukemia

C) Acute lymphoblastic leukemia

D) Bacterial infection

Infectious mononucleosis

15
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A patient has a prolonged non-therapeutic PT and a normal aPTT. The physician orders a PT mixing study. The results are as follows:

Original PT test- 32 seconds

1:1 Mix (room temp immediate) - 22 seconds

1:1 Mix (incubated for 90 minutes) - 23 seconds

Which factor may be present in abnormally low levels and causing the prolongation?

A) Factor XI

B) Factor VII

C) Factor IX

D) Factor VIII

Factor VII

16
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Which of the following bone marrow sampling methods would be advisable if the quantity is inadequate for an aspirate smear?

A) Touch imprint

B) Bone marrow core biopsy

C) Direct aspirate smear

D) Clot section

Touch imprint

17
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A complete blood count is performed on a post-surgical, post-transfusion patient. The red cell distribution width (RDW) reported with the automated cell count is 16.5%. The reference interval in this laboratory is 11.0-14.5%. What would be demonstrated on the peripheral smear that relates directly to the RDW value?

A) Anisocytosis

B) Macrocytosis

C) Microcytosis

D) Nucleated red blood cells

Anisocytosis

18
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Which of the following conditions can produce a normal aPTT and a prolonged PT?

A) Factor IX deficiency

B) Factor VII deficiency

C) Factor VIII deficiency

D) Factor X deficiency

Factor VII deficiency

19
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Which of the following factors is known as Hageman factor?

A) Factor X

B) Factor XII

C) Factor V

D) Factor VII

Factor XII

20
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The cells included in the composite image were found in the peripheral blood smear of a patient with the following results:

total WBC of 21.5 x 109/L.

Differential count:

metamyelocytes 4

band neutrophils 16

segmented neutrophils 48

monocytes 6

eosinophils 1

basophils 1

lymphocytes 24

This hematologic picture is most consistent with:

A) Leukemoid reaction

B) Chronic myeloid leukemia

C) Left shift

D) Leukoerythroblastosis

Left Shift

21
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Whole blood if composed of approximately:

A) 75% formed elements and 25% plasma

B) 60% formed elements and 40% plasma

C) 45% formed elements and 55% plasma

D) 30% formed elements and 70% plasma

45% formed elements and 55% plasma

22
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A known sickle cell trait patient has a hemoglobin electrophoresis test performed. Which of the following hemoglobin percentage sets would most closely match this patient's diagnostic state?

A) Hgb A = 90%, Hgb S = 8%, Hgb A2 = 2%, Hgb F = 0%

B) Hgb A = 60%, Hgb S = 38%, Hgb A2 = 2%, Hgb F = 0%

C) Hgb A = 40%, Hgb S = 58%, Hgb A2 = 2%, Hgb F = 0%

D) Hgb A = 25%, Hgb S = 70%, Hgb A2 = 2%, Hgb F = 3%

Hgb A = 60%, Hgb S = 38%, Hgb A2 = 2%, Hgb F = 0%

23
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The arrangement of the erythrocytes shown by the blue arrows in this peripheral smear should be reported out as ____________________ .

A) Agglutination

B) Rouleaux

C) Normal distribution

D) Aggregation

Agglutination

24
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Decrease platelet production can be caused by a lack of or decreased amount of which of the following?

A) Erythropoietin

B) Thrombopoietin

C) von Willebrand factor (vWF)

D) Factor VIII

Thrombopoietin

25
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Which of the following statements are true for the hematopoietic cords?

A) Hematopoietic cells develop at random locations in the marrow cells

B) Reticular cells (adventitial cells) provide support for developing hematopoietic cells within the hematopoietic cords

C) Lymphocytes are not seen in normal marrow

D) Fat cells content of bone marrow decrease with aging

Reticular cells (adventitial cells) provide support for developing hematopoietic cells within the hematopoietic cords

26
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An alpha thalassemia patient is diagnosed as having three of their four genes deleted which code for alpha hemoglobin chains. Which one of the following types of hemoglobin is abnormal and would be found in such a patient?

A) Hb A

B) Hb S

C) Hb F

D) Hb H

Hb H

27
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Calculate the red cell indices from the following set of patient data:

RBC count = 3.19 x 1012/L

Hemoglobin = 11.3 g/dL

Hematocrit = 35%

A) MCV = 99 fL, MCH = 38 pg, MCHC = 34 g/dL

B) MCV = 109 fL, MCH = 36 pg, MCHC = 34 g/dL

C) MCV = 110 fL, MCH = 35 pg, MCHC = 32 g/dL

D) MCV = 105 fL, MCH = 38 pg, MCHC = 32 g/dL

MCV = 110 fL, MCH = 35 pg, MCHC = 32 g/dL

28
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Which of the following conditions would be associated with an increased osmotic fragility test result?

A) Hereditary spherocytosis

B) Iron deficiency anemia

C) Sickle cell anemia

D) Thalassemia

Hereditary spherocytosis

29
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A peripheral smear with red blood cells photographed in a typical field was submitted for review. All of the following conditions are most likely associated with the red blood cell population found here, EXCEPT:

A) Severe liver disease

B) Hemoglobinopathy

C) Beta thalassemia

D) Hereditary Hemochromatosis

Hereditary Hemochromatosis

30
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The granules that basophils contain are composed of:

A) Histamine

B) Serotonin

C) Myeloperoxidase

D) Alkaline phosphatase

Histamine

31
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What is the best description of the phenomenon seen in this illustration?

A) Rouleau formation

B) Cold agglutination

C) Rosette formation

D) Monocyte activation

Rosette formation

32
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In the hemoglobin methodology using potassium ferricyanide the following measurable reaction occurs:

A) Carboxyhemoglobin is formed

B) Iron remains in the ferrous state

C) Ferrous iron is oxidized to ferric iron to form methemoglobin

D) Acid hematin is formed

Ferrous iron is oxidized to ferric iron to form methemoglobin

33
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All of the following CD markers are present on a normal mature T cell, EXCEPT?

A) CD20

B) CD7

C) CD3

D) CD5

CD20

34
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Fifty percent blasts are found on a peripheral blood smear. The cells are large (3-5x the size of a lymphocyte) with a nucleus that contains fine homogeneous chromatin and two to three nucleoli. There is moderate blue-grey cytoplasm with Auer rods. What leukemia is most likely?

A) Acute myelogenous leukemia (AML)

B) Hairy cell leukemia (HCL)

C) Acute lymphoblastic leukemia (ALL)

D) Chronic lymphocytic leukemia (CLL)

Acute myelogenous leukemia (AML)

35
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Which of the following inclusions are frequently seen on the same peripheral blood smear along with toxic granulation?

A) May-Hegglin bodies

B) Vacuoles

C) Auer rods

D) Primary granules

Vacuoles

36
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Which of the following laboratory results would be seen in a patient with acute Disseminated Intravascular Coagulation (DIC)?

A) Prolonged PT, decreased fibrinogen, elevated platelet count, increased FDP

B) Normal PT, decreased fibrinogen, decreased platelet count, decreased FDP

C) Prolonged PT, decreased fibrinogen, decreased platelet count, increased FDP

D) Normal PT, increased fibrinogen, decreased platelet count, decreased FDP

Prolonged PT, decreased fibrinogen, decreased platelet count, increased FDP

37
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Which of the following set of results would be consistent for a patient with the following findings: macrocytosis, anemia, leukopenia, and thrombocytopenia?

A) MCV 115 fL; Hgb 9.5 g/dL; WBC 6.5 x 103/µL; Platelets 75,000/µL

B) MCV 115 fL; Hgb 7.5 g/dL; WBC 2.5 x 103/µL; Platelets 75,000/µL

C) MCV 75 fL; Hgb 7.5 g/dL; WBC 2.5 x 103/µL; Platelets 75,000/µL

D) MCV 75 fL; Hgb 9.5 g/dL; WBC 6.5 x 103/µL; Platelets 175,000/µL

MCV 115 fL; Hgb 7.5 g/dL; WBC 2.5 x 103/µL; Platelets 75,000/µL

38
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Gastrointestinal infections of which of the following a organisms are associated with hemolytic uremic syndrome?

A) Shiga toxin producing E. coli

B) Salmonella

C) Proteus mirabilis

D) Clostridium difficile

Shiga toxin producing E. coli

39
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Which of the following statements is correct regarding bone marrow evaluation?

A) Bone marrow cellularity increases with age.

B) Bone marrow cellularity is highest in young children compared to adults.

C) In a healthy person, the expected myeloid : erythroid ratio is less than 1 (one).

D) As we age, the amount of adipose tissue (fat) decreases

Bone marrow cellularity is highest in young children compared to adults.

40
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The photomicrograph is a representative field from a peripheral blood smear. Which of the following MCV values correlates best with the peripheral blood picture?

A) 68 fL

B) 82 fL

C) 105 fL

D) 149 fL

105 fL

41
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A patient presents to the ER with prolonged bleeding. PT and aPTT tests both come back prolonged. After running Factor assays, it was determined the patient has Hemophilia B, also known as Christmas disease, a deficiency of which factor?

A) Factor VII

B) Factor VIII

C) Factor X

D) Factor IX

Factor IX

42
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Why is hereditary hemochromatosis (HH) thought to be underdiagnosed?

A) Its early symptoms are nonspecific and vague, and generally do not get serious until later in life.

B) It is an extremely rare disease.

C) It appears shortly after birth, but then symptoms rapidly subside.

D) It is a mild disorder and has no severe implications for one's health.

Its early symptoms are nonspecific and vague, and generally do not get serious until later in life.

43
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Which of the following is the most common method for diagnosing malaria?

A) Serological testing

B) Polymerase chain reaction (PCR) techniques

C) Demonstration of the organism in peripheral blood

D) Biochemical reactions

Demonstration of the organism in peripheral blood

44
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When scanning a Wright's stained blood smear, which of the following would describe the optimum area to begin your blood smear analysis and differential white blood cell count?

A) RBCs are fairly far apart showing a "cobblestone effect."

B) RBCs are lying singly, barely touching, with occasional overlapping.

C) RBCs are stacked like coins with the majority of cells overlapping.

D) RBCs are aggregated.

RBCs are lying singly, barely touching, with occasional overlapping.

45
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Four tubes of CSF on the same patient were received in the laboratory. It was noted on the report that all four tubes contained visible blood. Which of the following is the best explanation for this finding?

A) Traumatic tap

B) Subarachnoid hemorrhage

C) Meningitis

D) WAHA

Subarachnoid hemorrhage

46
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Which of the following stains is used to differentiate a neutrophilic leukemoid reaction from chronic myelogenous leukemia (CML)?

A) Sudan black B

B) Periodic acid-Schiff reagent (PAS)

C) Acid phosphatase with tartrate

D) Leukocyte alkaline phosphatase (LAP)

Leukocyte alkaline phosphatase (LAP)

47
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Which of the following laboratory test results indicates that a sickle cell patient may be in aplastic crisis?

A) Decreased reticulocyte count

B) Decreased haptoglobin level

C) Increased bilirubin level

D) Increased lactate dehydrogenase (LDH)

Decreased reticulocyte count

48
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Blood is diluted at 1:100 and charged on the hemocytometer counting chambers on both sides. If the average platelet count from a counting chamber in one mm2 (one large square) is 68, what is the calculated platelet count?

A) 680,000/mm3

B) 6,800/mm3

C) 68,000/mm3

D) 34,000/mm3

68,000/mm3

49
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Consider the following set of results from a mixing study of a patient with a suspected coagulopathy.

Initial aPTT: 86 sec. (reference range 21-34 sec.)

Immed. aPTT mixing study: 87 sec.

Incubated aPTT mixing study: 88 sec.

What is the most likely cause of these results?

A) The assay corrected, indicating a likely coagulation factor deficiency.

B) The assay corrected, indicating a likely coagulation inhibitor.

C) The assay did not correct, indicating a likely coagulation factor deficiency.

D) The assay did not correct, indicating a likely coagulation inhibitor.

The assay did not correct, indicating a likely coagulation inhibitor.

50
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Hematocrit is:

A) Percentage of blood made up of serum

B) Concentration of serum X 100

C) Percentage of blood made up of red blood cells

D) Concentration of red cells X 100

Percentage of blood made up of red blood cells

51
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All of the following disorders would affect the results of a Prothrombin time (PT) EXCEPT?

A) Factor VIII deficiency

B) Coumadin therapy

C) Vitamin K deficiency

D) Alcoholic cirrhosis

Factor VIII deficiency

52
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This image represents a field of red blood cells (RBCs) stained using a supravital stain. How would these cells appear if viewed on a Wright-stained smear?

A) Polychromatophilic RBCs

B) RBCs containing basophilic stippling

C) RBCs containing Cabot's rings

D) RBCs containing Pappenheimer bodies

Polychromatophilic RBCs

53
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When performing a manual white blood cell count, 236 cells were counted on side number one of the hemacytometer, 224 cells on side number two. A 1/20 dilution of 1% HC1 was used, and the area counted on each side was 4 sq. mm. Twenty-five nucleated red blood cells in the differential were observed per 100 white blood cells. What is the CORRECT WBC/µL?

A) 8,500

B) 9,200

C) 9,575

D) 12,425

9,200

54
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This image depicts a brilliant cresyl blue-stained blood smear. What inclusion bodies are shown in the erythrocyte indicated by the arrow (B)?

A) Howell-Jolly bodies

B) Hb H inclusions

C) Pappenheimer bodies

D) Siderotic granules

Hb H inclusions

55
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What RBC morphology on a Wright-stained smear may indicate the presence of an unstable hemoglobin?

A) Acanthocytes

B) Codocytes

C) Schistocytes

D) Xerocytes

Schistocytes

56
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What are Howell-Jolly bodies composed of?

A) Hemoglobin

B) DNA

C) Iron

D) RNA

DNA

57
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All of the following factors would cause an increase erythrocyte sedimentation rate (ESR) values EXCEPT?

A) Severe anemia

B) Abnormal proteins (Rouleaux)

C) Blood drawn into sodium citrate anticoagulant

D) A slanted (not perpendicular) tube

Blood drawn into sodium citrate anticoagulant

58
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When performing your mixing study, you aliquot your sample plasma and the pooled normal plasma to create your "mix." You then place the sample in a water bath to incubate for 90 minutes before running your new mixed sample. What is the problem with the steps involved in the procedure above?

A) You don't need to incubate your sample.

B) You have forgotten to add a reagent.

C) You have not run a PT or aPTT on the new mix before incubating.

D) You have incubated too long.

You have not run a PT or aPTT on the new mix before incubating.

59
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How is beta thalassemia defined?

A) A decrease in the rate of production of beta chains due to a partial or total deletion of loci from chromosome 16 that code for the beta chain.

B) A decrease in the rate of production of Hb A due to a substitution of an amino acid in the beta chain.

C) A decrease in the rate of production of beta chains due to a partial or total deletion of loci from chromosome 11 that code for the beta chain.

D) The production of an abnormal form of hemoglobin due to the substitution of an amino acid in the beta chain.

A decrease in the rate of production of beta chains due to a partial or total deletion of loci from chromosome 11 that code for the beta chain.

60
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The MOST accurate observation about osmotic pressure is that it is:

A) Proportional to concentration of solute particles

B) Equal to number of solvent molecules times a factor

C) Measurable by how much it raises the freezing point of water

D) Directly proportional to the inverse log of solvent molecules

Proportional to concentration of solute particles

61
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What is the identity of the white blood cell inclusions present in this image?

A) Toxic granulation

B) May-Hegglin bodies

C) Auer rods

D) Barr bodies

Toxic granulation

62
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This autosomal recessive disorder is associated with recurrent bacterial infections and cells consistent with the cell in the image.

A) Alder-Reilly anomaly

B) May-Hegglin anomaly

C) Chediak-Higashi syndrome

D) Pelger-Huet anomaly

Chediak-Higashi syndrome

63
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Which of the following cells is the most common nucleated cell in normal adult bone marrow?

A) Myeloblast

B) Promyelocyte

C) Myelocyte

D) Metamyelocyte

Metamyelocyte

64
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What is the prominent red blood cell (RBC) morphologic feature found in lead poisoning (plumbism)?

A) Basophilic stippling

B) Hypersegmentation

C) Macrocytosis

D) Target cell

Basophilic stippling

65
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What are the red cell inclusions in this split frame photomicrograph of peripheral smears (Wright's and Prussian Blue)?

A) Howell-Jolly bodies

B) Basophilic stippling

C) Malarial ring forms

D) Pappenheimer bodies

Pappenheimer bodies

66
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The structure indicated by the arrow in this image, along with giant platelets (also present in the image), is characteristic of which of the following conditions?

A) Chediak-Higashi anomaly

B) Alder-Reilly anomaly

C) May-Hegglin anomaly

D) Infectious Mononucleosis

May-Hegglin anomaly

67
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A newly admitted patient has the following coagulation results:

PT: 12.9 seconds (N = 12-14 seconds)

aPTT: 84 seconds (N = 25-35 seconds)

Platelet Count: 200 x 109/L (N = 150-450 x 109/L)

A mixing study was performed due to the abnormal aPTT test results. The mixing study demonstrated the following:

aPTT was corrected by normal plasma, factor IX deficient plasma, but not by factor VIII deficient plasma.

What factor assay should be performed next?

A) None; a platelet disorder is indicated

B) Factor V assay

C) Factor VIII assay

D) Factor IX assay

Factor VIII assay

68
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A patient's coagulation mixing study results are shown below after an initially prolonged aPTT result.

Initial aPTT: 63 sec. (normal range 21-34 seconds)

Immediate aPTT mixing study: 26 sec.

Incubated aPTT mixing study: 65 sec.

Has the aPTT been corrected by the mix? Is a factor deficiency or a coagulation inhibitor the more likely cause of the patient's prolonged aPTT?

A) Corrected, Factor Deficiency

B) Corrected, Coagulation Inhibitor

C) Not Corrected, Factor Deficiency

D) Not Corrected, Coagulation Inhibitor

Not Corrected, Coagulation Inhibitor

69
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In which of the following conditions would you NOT expect to find Howell-Jolly bodies?

A) Sickle cell anemia

B) Iron deficiency anemia

C) Post splenectomy

D) Megaloblastic anemia

Iron deficiency anemia

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A technologist decides to make a 1:20 dilution of cerebrospinal fluid (CSF) after briefly evaluating a portion of the sample microscopically. After making the dilution and charging the chambers, the number of observed cells in each of the large squares of the hemocytometer is >100. What should the technologist do to obtain the most accurate count?

A) Count all four corner squares.

B) Make a smaller dilution.

C) Make a larger dilution.

D) No dilution is necessary.

Make a larger dilution.

71
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A 55-year-old white male had the following lab data:

RBC 3.7 X 1012/L

Serum iron 220 µg/dL (N: 60-80 µg/dL)

TIBC 300 µg/dL (N: 260-400 µg/dL)

Hct 32%

Serum Ferritin 2,800 ng/mL (N: 10-200 ng/mL)

WBC 5.8 x 109/L

MCV 86 fL

MCH 26 pg

MCHC 32%

Prussian Blue stain of bone marrow aspirate indicates markedly elevated iron stores.

These laboratory results are MOST consistent with which of the following conditions?

A) Sideroblastic anemia

B) Anemia of chronic disease

C) Hemochromatosis

D) Megaloblastic anemia

Hemochromatosis

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One of the most common forms of hereditary hemochromatosis has been found to result from genetic mutations of the HFE gene. This mutation causes hemochromatosis by which of the following mechanisms?

A) Impairs hepcidin regulation of ferroportin activity

B) Increased binding of ß2 microglobulin

C) Impairs transferrin synthesis

D) Increases hepcidin synthesis therefore increasing iron absorption.

Impairs hepcidin regulation of ferroportin activity

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Which of the following leukocytes is most directly associated with antibody production?

A) B-Cell

B) T-Cell

C) Neutrophil

D) NK Cell

B-Cell

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All of the following are causes of hemolytic anemia, EXCEPT?

A) Thermal injury

B) Iron deficiency anemia

C) Brown recluse spider bite

D) Plasmodium infection

Iron deficiency anemia

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Which disease/condition can be indicated by the morphology displayed in the white blood cell to the right?

A) Chediak-Higashi syndrome

B) Pelger-Huet anomaly

C) Dohle bodies

D) Toxic granulation

Chediak-Higashi syndrome

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The granules of Basophil contain which of the following?

A) Antihistamine

B) IgE

C) The contents of helminth digestion

D) Initiators of allergic inflammation

Initiators of allergic inflammation

77
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Electrophoretic separation of hemoglobin fundamentally relies on:

A) Weight differences of molecules

B) Electrical charge differences of molecules

C) Concentration differences of molecules

D) Shape variations of molecules

Electrical charge differences of molecules

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Methods of identifying many of the major hemoglobin variants such as Hb A, Hb F, Hb S, etc. include all of the following EXCEPT:

A) Sodium metabisulfite solubility test

B) High performance liquid chromatography (HPLC)

C) Citrate agar electrophoresis

D) Alkaline electrophoresis

Sodium metabisulfite solubility test

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A patient with suspected intraabdominal malignancy had a paracentesis procedure performed. The fluid was then sent to the laboratory for examination and fluid differential. Which cells predominate in this cytospin field from the patient's sample?

A) Monocytes

B) Atypical lymphocytes

C) Blasts

D) Plasma cells

Plasma cells

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Approximately what percentage of pulmonary emboli originate from deep veins of the legs?

A) 65%

B) 75%

C) 85%

D) 95%

95%

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Calculate the mean corpuscular hemoglobin content (MCHC) when Hgb = 15 g/dL (150 g/L), RBC count = 4.50 x 106/µL (4.50 x 1012/L), and Hct = 47% (0.47).

A) 34.7 g/dL

B) 10.4 g/dL

C) 31.9 g/dL

D) 33.9 g/dL

31.9 g/dL

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The three main types of peripheral blood cells are:

A) White blood cells, red platelets, and thrombocytes

B) White blood cells, red blood cells, and platelets

C) Leukocytes, erythrocytes, red blood cells

D) Thrombocytes, platelets, and leukocytes

White blood cells, red blood cells, and platelets

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After experiencing crippling pain in her chest, Elizabeth's mother rushes her to the Emergency Room. After a complete blood count and differential are ordered, the hematology technologist views many peripheral cells similar in appearance to those found in the image below. Which condition is most likely present?

A) Beta Thalassemia

B) Myocardial Infarction

C) Sickle Cell Anemia

D) Hemoglobin C Disease

Sickle Cell Anemia

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Adult (normal) Hemoglobin is made up of the following composition:

A) >90% HbA, 1% HbA2, 5% HbF

B) >95% HbA,

>95% HbA,

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How many 1 mm x 1 mm squares is the Neubauer hemacytometer counting grid composed of?

A) Nine per side

B) Ten per side

C) Twenty-two between both sides

D) Thirty between both sides

Nine per side

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Which statement best describes the relationship between dietary iron and iron absorption in a healthy individual?

A) Only a small percentage of dietary iron is absorbed and used.

B) All dietary iron is needed for hemoglobin synthesis and therefore absorbed.

C) Most people need to take dietary iron supplements to meet their needs for iron.

D) All dietary iron is absorbed and excess is stored.

Only a small percentage of dietary iron is absorbed and used.

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Which one of the following is a true statement about Lupus Anticoagulant (LA)?

A) LA is a specific inhibitor found mainly in patients with the autoimmune disease, Systemic Lupus Erythematosus (SLE).

B) LA is common in hemophiliacs

C) LA prolongs coagulation leading to bleeding problems in patients.

D) LA is an immunoglobulin.

LA is an immunoglobulin.

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All of the following conditions are consistent with this peripheral blood picture, EXCEPT?

A) Abetalipoproteinemia

B) Alcoholic cirrhosis with hemolytic anemia

C) Hepatitis of the newborn

D) Post-splenectomy

Abetalipoproteinemia

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A small child has albino characteristics, photophobia, frequent pyogenic infections, and her blood smear shows giant dark granules in her monocytes and granulocytes. What is the probable diagnosis?

A) Pelger-Huet anomaly

B) Alder-Reilly

C) Toxic granulation

D) Chediak-Hegashi syndrome

Chediak-Hegashi syndrome

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A patient with multiple myeloma is admitted to the hospital due to a flare-up of symptoms. Her physician orders a complete blood count with differential. The peripheral blood smear is shown. Which morphology is consistent with the findings in this case?

A) Rouleaux

B) Agglutination

C) Polychromasia

D) Hypochromia

Rouleaux

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Which one of these test systems can be used to evaluate the adequacy of fibrinogen in heparinized patients?

A) D-Dimer

B) Reptilase Time

C) Thrombin Time

D) Prothrombin Time

Reptilase Time

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If a Mycobacterium sp. infection is suspected on a bone marrow or body fluid, what stain should be used to detect these bacteria?

A) Wright's stain

B) New methylene blue stain

C) Hematoxylin and Eosin (H&E) stain

D) Acid fast stain

Acid fast stain

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Which of the following is the cause of thrombotic thrombocytopenic purpura (TTP)?

A) Thrombopoietin (TPO) deficiency

B) ADAMTS13 deficiency

C) Platelet antibodies

D) The cause of TTP is idiopathic

ADAMTS13 deficiency

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All of the following are ways hemoglobin functions EXCEPT:

A) Transport Oxygen

B) Transport Carbon Dioxide

C) Transport Nitric Oxide

D) Transport Haptoglobin

Transport Haptoglobin

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Which of the following processes can lead to the formation of microclots in a patient specimen that is collected in a tube containing EDTA anticoagulant?

A) Failing to invert the tube after specimen collection.

B) Filling the tube as full as the vacuum in the tube allows.

C) Inverting the tube 5 - 10 times after specimen collection.

D) Using the EDTA tube for an automated platelet count.

Failing to invert the tube after specimen collection.

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How long are healthy neutrophils expected to reside in the peripheral blood of an adult?

A) 3 days

B) 1 day

C) 7-8 hours

D) 12-14 hours

7-8 hours

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If the red cell count is known, which of the following MUST also be known in order to calculate the mean corpuscular volume (MCV)?

A) Hemoglobin

B) Leukocyte count

C) Reticulocyte count

D) Hematocrit

Hematocrit

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The diagram above represents which of the following beta thalassemias?

A) Beta thalassemia minor

B) Beta thalassemia intermedia

C) Beta thalassemia major

D) Beta thalassemia minima

Beta thalassemia intermedia

This diagram represents ßo/ß+ beta thalassemia intermedia. It is intermedia even though one locus is deleted because only a small part of the remaining locus is missing. Beta thalassemia intermedia (ßo/ß+, ß+/ß+, or ßo/ß) causes a moderate anemia.

ß+/ß denotes one partially deleted or inactive beta chain gene and one fully functional beta gene. This results in beta thalassemia minor (ßo/ß can also phenotype as beta thalassemia minor). This genotype causes decreased production of beta chains and a mild, asymptomatic anemia.

Beta thalassemia major (ßo/ßo, ßo/ß+, or ß+/ß+ ), also known as Cooley's anemia, causes a severe anemia approximately six months after birth.

Beta thalassemia minima (ßsc/ß) is an asymptomatic beta thalassemia (silent carrier).

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The mediator cell type that binds to IgE antibodies is the:

A) Basophil

B) Eosinophil

C) Polymorphonuclear neutrophil (PMN)

D) Macrophage

Basophil

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The large cell shown in the illustration to the right is occasionally seen in the bone marrow and can be mistaken for a plasma cell. What is this cell?

A) Myeloblast

B) Osteoblast

C) Stem cell

D) Megakaryoblast

Osteoblast