Deck 5: Hematology

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سؤال
Which of the following statements regarding Pro time testing is false?

A) The major use of the Pro time test is to monitor patients who have been placed on anticoagulant therapy.
B) Patients taking anticoagulants will have lower Pro time and international normalized ratio (INR) results.
C) Patients with low Pro time results are in danger of internal clotting, which can cause strokes and heart attacks.
D) Patients who lack clotting factors, have liver disease, or are deficient in vitamin K will have higher Pro time results.
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سؤال
The erythrocyte indices:

A) aid in diagnosing anemia classifications.
B) provide information for hematocrit.
C) allow for calculations of oxygen in hemoglobin.
D) compare the RBC count to the WBC count.
E) are taken from the ESR results.
سؤال
Which of the following statements regarding erythrocyte sedimentation rate (ESR) is false?

A) The following technical interferences will increase the ESR result: vibrating surface, reading after 60 minutes, and tilting the sedimentation rate tube.
B) When plasma proteins increase, they cause the RBCs to stack together like poker chips, a condition known as rouleaux.
C) ESR tests cannot be performed on capillary blood because of the volume of blood needed.
D) The following medical conditions will cause a decreased ESR result: inflammatory diseases, autoimmune disorders, cancer, and leukemia.
سؤال
Which of the following WBCs does not match the associated description?

A) Basophil becomes a mast cell when it enters the tissues to mediate the inflammatory response.
B) Lymphocyte is the smallest WBC.
C) Eosinophil increases in number during allergic reactions.
D) Neutrophil can differentiate into a T cell or B cell.
E) Monocyte is the largest WBC.
سؤال
Which of the following statements regarding hematocrits is false?

A) If capillary blood from a finger is used for the microhematocrit, the capillary tube must not contain an anticoagulant.
B) Spun hematocrits should be performed in duplicate, with results falling within 2% of each other.
C) Note the appearance of the plasma for hemolysis (red) and/or lipemia (cloudy white due to high fat content).
D) One condition in which a high hematocrit value might be found is polycythemia.
سؤال
The complete blood count (CBC) generally includes all of the following except:

A) hemoglobin.
B) hematocrit.
C) ESR.
D) RBC count.
E) WBC count.
سؤال
Hematology is the study of:

A) blood chemistry.
B) proteins in the blood.
C) blood plasma.
D) formed elements in the blood and bone marrow.
E) infectious diseases in the blood.
سؤال
Which term does not match its description?

A) Erythrocytes are the most numerous blood cells, occupying almost 50% of blood volume.
B) Bands are immature neutrophils.
C) Platelets are fragments of cytoplasm.
D) Segs are mature neutrophils.
E) Basophils have coarse red granules in their cytoplasm.
سؤال
Which of the following is not a granulocyte?

A) Eosinophil
B) Neutrophil
C) Lymphocyte
D) Basophil
E) Band/seg
سؤال
The major component in the erythrocyte that carries oxygen is:

A) hematocrit.
B) hemoglobin.
C) plasma.
D) protein.
E) iron.
سؤال
Which of the following statements regarding the making and staining of a blood smear is true?

A) When identifying cells, one should note the size, shape, and color of the blood cell, its nucleus, and its cytoplasm.
B) Blood cells are observed and identified under the low power lens of the microscope.
C) A properly done blood smear will have a blunt edge at the end of the smear and a thinner distribution of blood cells in the heel of the slide.
D) Medical assistants are qualified to read and report a stained blood smear.
سؤال
Most CLIA-waived hematology tests use blood from a(n):

A) artery.
B) vein.
C) capillary.
D) Vacutainer.
E) syringe.
سؤال
Which of the following is not a formed element in the blood?

A) Prothrombin
B) White blood cells (WBCs)
C) Red blood cells (RBCs)
D) Platelets
سؤال
A critical vitamin used by the liver to produce clotting factors is vitamin:

A) A.
B) D.
C) E.
D) B.
E) K.
سؤال
The anticoagulant and Vacutainer tube used for most hematology testing in a reference lab is:

A) heparin in a green-top tube.
B) heparin in a lavender-top tube.
C) ethylenediaminetetraacetic acid (EDTA) in a green-top tube.
D) EDTA in a lavender-top tube.
E) none of these; no anticoagulant is needed for hematology tests.
سؤال
Match between columns
Increase in WBCs (usually due to infection)
Mononucleosis
Increase in WBCs (usually due to infection)
ALL (acute lymphocytic leukemia)
Increase in WBCs (usually due to infection)
CML (chronic myelocytic leukemia)
Increase in WBCs (usually due to infection)
Leukocytosis
Increase in WBCs (usually due to infection)
Leukocytopenia
Presence of atypical "reactive" lymphocytes
Mononucleosis
Presence of atypical "reactive" lymphocytes
CML (chronic myelocytic leukemia)
Presence of atypical "reactive" lymphocytes
Leukocytosis
Presence of atypical "reactive" lymphocytes
Leukocytopenia
Presence of atypical "reactive" lymphocytes
Mononucleosis
Long-term cancer of granulocytes in bone marrow
CML (chronic myelocytic leukemia)
Long-term cancer of granulocytes in bone marrow
ALL (acute lymphocytic leukemia)
Long-term cancer of granulocytes in bone marrow
Leukocytosis
Long-term cancer of granulocytes in bone marrow
Leukocytopenia
Long-term cancer of granulocytes in bone marrow
Mononucleosis
Abnormal decrease of WBCs
Leukocytopenia
Abnormal decrease of WBCs
Leukocytosis
Abnormal decrease of WBCs
CML (chronic myelocytic leukemia)
Abnormal decrease of WBCs
ALL (acute lymphocytic leukemia)
Abnormal decrease of WBCs
ALL (acute lymphocytic leukemia)
Sudden cancer of a nongranulocyte
Mononucleosis
Sudden cancer of a nongranulocyte
Leukocytopenia
Sudden cancer of a nongranulocyte
Leukocytosis
Sudden cancer of a nongranulocyte
CML (chronic myelocytic leukemia)
Sudden cancer of a nongranulocyte
ALL (acute lymphocytic leukemia)
سؤال
Match between columns
Seen with blood loss (menses, ulcers, hemorrhaging)
Iron deficiency anemia
Seen with blood loss (menses, ulcers, hemorrhaging)
Hemolytic anemia
Seen with blood loss (menses, ulcers, hemorrhaging)
Sickle cell anemia
Seen with blood loss (menses, ulcers, hemorrhaging)
Pernicious anemia
Seen with blood loss (menses, ulcers, hemorrhaging)
Aplastic anemia
Inherited abnormal hemoglobin S
Iron deficiency anemia
Inherited abnormal hemoglobin S
Hemolytic anemia
Inherited abnormal hemoglobin S
Sickle cell anemia
Inherited abnormal hemoglobin S
Pernicious anemia
Inherited abnormal hemoglobin S
Aplastic anemia
Destruction of stem cells in bone marrow from toxins
Iron deficiency anemia
Destruction of stem cells in bone marrow from toxins
Hemolytic anemia
Destruction of stem cells in bone marrow from toxins
Sickle cell anemia
Destruction of stem cells in bone marrow from toxins
Pernicious anemia
Destruction of stem cells in bone marrow from toxins
Aplastic anemia
Caused by decreased vitamin B12
Iron deficiency anemia
Caused by decreased vitamin B12
Hemolytic anemia
Caused by decreased vitamin B12
Sickle cell anemia
Caused by decreased vitamin B12
Pernicious anemia
Caused by decreased vitamin B12
Aplastic anemia
Destruction of circulating RBCs
Iron deficiency anemia
Destruction of circulating RBCs
Hemolytic anemia
Destruction of circulating RBCs
Sickle cell anemia
Destruction of circulating RBCs
Pernicious anemia
Destruction of circulating RBCs
Aplastic anemia
سؤال
Match between columns
MCH (mean cell hemoglobin)
Hgb/HCT (31% to37% or g/dL)
MCH (mean cell hemoglobin)
Hgb/RBC (26 to34 pg)
MCH (mean cell hemoglobin)
Hgb/HCT (31% to37% or g/dL)
MCHC (mean cell hemoglobin concentration)
HCT/RBC (82 to98 micrometers/fL)
MCHC (mean cell hemoglobin concentration)
Hgb/RBC (26 to34 pg)
MCHC (mean cell hemoglobin concentration)
HCT/RBC (82 to98 micrometers/fL)
MCV (mean cell volume)
Hgb/HCT (31% to37% or g/dL)
MCV (mean cell volume)
Hgb/RBC (26 to34 pg)
MCV (mean cell volume)
HCT/RBC (82 to98 micrometers/fL)
سؤال
Match between columns
Abnormal decrease in RBCs
Leukopenia
Abnormal decrease in RBCs
Anemia
Abnormal decrease in RBCs
Leukemia
Abnormal decrease in RBCs
Leukocytosis
Abnormal decrease in RBCs
Polycythemia
Cancer of the WBCs
Anemia
Cancer of the WBCs
Leukopenia
Cancer of the WBCs
Leukemia
Cancer of the WBCs
Leukocytosis
Cancer of the WBCs
Polycythemia
Abnormal increase in WBCs
Anemia
Abnormal increase in WBCs
Leukopenia
Abnormal increase in WBCs
Leukemia
Abnormal increase in WBCs
Leukocytosis
Abnormal increase in WBCs
Polycythemia
Abnormal decrease in WBCs
Anemia
Abnormal decrease in WBCs
Leukopenia
Abnormal decrease in WBCs
Leukemia
Abnormal decrease in WBCs
Leukocytosis
Abnormal decrease in WBCs
Polycythemia
Abnormal increase in RBCs
Anemia
Abnormal increase in RBCs
Leukopenia
Abnormal increase in RBCs
Leukemia
Abnormal increase in RBCs
Leukocytosis
Abnormal increase in RBCs
Polycythemia
سؤال
Match between columns
HemoCue
Hematocrit (HCT)
HemoCue
Sedimentation rate
HemoCue
Coagulation test
HemoCue
Hemoglobin (Hgb)
HemoCue
CBC
Sediplast/Westergren/Streck
Hematocrit (HCT)
Sediplast/Westergren/Streck
Sedimentation rate
Sediplast/Westergren/Streck
Coagulation test
Sediplast/Westergren/Streck
Hemoglobin (Hgb)
Sediplast/Westergren/Streck
CBC
HemataSTAT
CBC
HemataSTAT
Hemoglobin (Hgb)
HemataSTAT
Coagulation test
HemataSTAT
Sedimentation rate
HemataSTAT
Hematocrit (HCT)
QBC
Sedimentation rate
QBC
Coagulation test
QBC
Hemoglobin (Hgb)
QBC
CBC
QBC
Hematocrit (HCT)
Pro time
Hematocrit (HCT)
Pro time
Sedimentation rate
Pro time
Coagulation test
Pro time
Hemoglobin (Hgb)
Pro time
CBC
سؤال
Match between columns
Pro time
36% to55%
Pro time
12 to18 g/dL
Pro time
36% to55%
Pro time
0 to20 mm/hour
ESR
1.0 INR
ESR
12 to18 g/dL
ESR
0 to20 mm/hour
ESR
1.0 INR
Hemoglobin
12 to18 g/dL
Hemoglobin
36% to55%
Hemoglobin
0 to20 mm/hour
Hemoglobin
1.0 INR
Hematocrit
12 to18 g/dL
Hematocrit
36% to55%
Hematocrit
0 to20 mm/hour
Hematocrit
1.0 INR
سؤال
Match between columns
RBC layer
Label C
RBC layer
Label C
RBC layer
Label B
RBC layer
Label D
RBC layer
Label E
Air
Label A
Air
Label C
Air
Label B
Air
Label D
Air
Label E
Buffy layer
Label A
Buffy layer
Label C
Buffy layer
Label B
Buffy layer
Label D
Buffy layer
Label E
Clay sealant
Label A
Clay sealant
Label C
Clay sealant
Label B
Clay sealant
Label D
Clay sealant
Label E
Plasma
Label A
Plasma
Label B
Plasma
Label D
Plasma
Label E
Plasma
Label A
سؤال
Match between columns
A byproduct of RBC breakdown that is sent to the liver
Anemia
A byproduct of RBC breakdown that is sent to the liver
Heme
A byproduct of RBC breakdown that is sent to the liver
Globin
A byproduct of RBC breakdown that is sent to the liver
Bilirubin
A byproduct of RBC breakdown that is sent to the liver
Hemoglobin
The protein portion of the hemoglobin molecule
Hemoglobin
The protein portion of the hemoglobin molecule
Bilirubin
The protein portion of the hemoglobin molecule
Globin
The protein portion of the hemoglobin molecule
Heme
The protein portion of the hemoglobin molecule
Anemia
The iron portion of the hemoglobin molecule
Hemoglobin
The iron portion of the hemoglobin molecule
Bilirubin
The iron portion of the hemoglobin molecule
Anemia
The iron portion of the hemoglobin molecule
Globin
The iron portion of the hemoglobin molecule
Heme
A condition in which the RBC or hemoglobin levels are below normal
Anemia
A condition in which the RBC or hemoglobin levels are below normal
Hemoglobin
A condition in which the RBC or hemoglobin levels are below normal
Bilirubin
A condition in which the RBC or hemoglobin levels are below normal
Globin
A condition in which the RBC or hemoglobin levels are below normal
Heme
A molecule that has a reddish pigment and is capable of carrying oxygen
Anemia
A molecule that has a reddish pigment and is capable of carrying oxygen
Hemoglobin
A molecule that has a reddish pigment and is capable of carrying oxygen
Bilirubin
A molecule that has a reddish pigment and is capable of carrying oxygen
Globin
A molecule that has a reddish pigment and is capable of carrying oxygen
Heme
سؤال
Match between columns
Activates prothrombin to become thrombin
Thrombin
Activates prothrombin to become thrombin
Thromboplastin
Activates prothrombin to become thrombin
Fibrin
Activates prothrombin to become thrombin
Thrombin
Activates prothrombin to become thrombin
Heparin
A natural anticoagulant that prevents excessive clotting
Embolus
A natural anticoagulant that prevents excessive clotting
Thromboplastin
A natural anticoagulant that prevents excessive clotting
Fibrin
A natural anticoagulant that prevents excessive clotting
Heparin
A natural anticoagulant that prevents excessive clotting
Embolus
The final sticky, stringy product of coagulation
Thromboplastin
The final sticky, stringy product of coagulation
Fibrin
The final sticky, stringy product of coagulation
Thrombin
The final sticky, stringy product of coagulation
Heparin
The final sticky, stringy product of coagulation
Embolus
Activates fibrinogen to become fibrin
Thromboplastin
Activates fibrinogen to become fibrin
Fibrin
Activates fibrinogen to become fibrin
Thrombin
Activates fibrinogen to become fibrin
Heparin
Activates fibrinogen to become fibrin
Embolus
A moving clot
Thromboplastin
A moving clot
Fibrin
A moving clot
Thrombin
A moving clot
Heparin
A moving clot
Embolus
سؤال
Match between columns
Many-shaped nucleus or "seg"
Nongranulocytes
Many-shaped nucleus or "seg"
Myeloblast
Many-shaped nucleus or "seg"
Megakaryocyte
Many-shaped nucleus or "seg"
Macrophages
Many-shaped nucleus or "seg"
Nongranulocytes
Lymphocyte and monocyte group
Polymorphonuclear
Lymphocyte and monocyte group
Myeloblast
Lymphocyte and monocyte group
Megakaryocyte
Lymphocyte and monocyte group
Macrophages
Lymphocyte and monocyte group
Nongranulocytes
Large nuclear cell in the bone marrow that fragments its cytoplasm to become platelets
Polymorphonuclear
Large nuclear cell in the bone marrow that fragments its cytoplasm to become platelets
Myeloblast
Large nuclear cell in the bone marrow that fragments its cytoplasm to become platelets
Megakaryocyte
Large nuclear cell in the bone marrow that fragments its cytoplasm to become platelets
Macrophages
Large nuclear cell in the bone marrow that fragments its cytoplasm to become platelets
Polymorphonuclear
WBC stem cell that develops into the three kinds of granulocytes
Myeloblast
WBC stem cell that develops into the three kinds of granulocytes
Megakaryocyte
WBC stem cell that develops into the three kinds of granulocytes
Macrophages
WBC stem cell that develops into the three kinds of granulocytes
Nongranulocytes
WBC stem cell that develops into the three kinds of granulocytes
Polymorphonuclear
Large engulfing cells in the tissues that came from monocytes
Myeloblast
Large engulfing cells in the tissues that came from monocytes
Megakaryocyte
Large engulfing cells in the tissues that came from monocytes
Macrophages
Large engulfing cells in the tissues that came from monocytes
Nongranulocytes
Large engulfing cells in the tissues that came from monocytes
Polymorphonuclear
سؤال
Match between columns
Newly released RBCs into the blood that still contain some nuclear DNA
Anisocytosis
Newly released RBCs into the blood that still contain some nuclear DNA
Reticulocytes
Newly released RBCs into the blood that still contain some nuclear DNA
Poikilocytosis
Newly released RBCs into the blood that still contain some nuclear DNA
Hematologists
Newly released RBCs into the blood that still contain some nuclear DNA
Erythroblast
Immature red cell in bone marrow (also called rubriblast)
Anisocytosis
Immature red cell in bone marrow (also called rubriblast)
Reticulocytes
Immature red cell in bone marrow (also called rubriblast)
Poikilocytosis
Immature red cell in bone marrow (also called rubriblast)
Hematologists
Immature red cell in bone marrow (also called rubriblast)
Erythroblast
Variances in RBC size
Anisocytosis
Variances in RBC size
Reticulocytes
Variances in RBC size
Poikilocytosis
Variances in RBC size
Erythroblast
Variances in RBC size
Hematologists
Abnormally shaped
Erythroblast
Abnormally shaped
Anisocytosis
Abnormally shaped
Reticulocytes
Abnormally shaped
Poikilocytosis
Abnormally shaped
Hematologists
Specialists who evaluate the cellular elements of blood microscopically and analytically
Erythroblast
Specialists who evaluate the cellular elements of blood microscopically and analytically
Anisocytosis
Specialists who evaluate the cellular elements of blood microscopically and analytically
Reticulocytes
Specialists who evaluate the cellular elements of blood microscopically and analytically
Poikilocytosis
Specialists who evaluate the cellular elements of blood microscopically and analytically
Hematologists
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ملء الشاشة (f)
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Deck 5: Hematology
1
Which of the following statements regarding Pro time testing is false?

A) The major use of the Pro time test is to monitor patients who have been placed on anticoagulant therapy.
B) Patients taking anticoagulants will have lower Pro time and international normalized ratio (INR) results.
C) Patients with low Pro time results are in danger of internal clotting, which can cause strokes and heart attacks.
D) Patients who lack clotting factors, have liver disease, or are deficient in vitamin K will have higher Pro time results.
B
2
The erythrocyte indices:

A) aid in diagnosing anemia classifications.
B) provide information for hematocrit.
C) allow for calculations of oxygen in hemoglobin.
D) compare the RBC count to the WBC count.
E) are taken from the ESR results.
A
3
Which of the following statements regarding erythrocyte sedimentation rate (ESR) is false?

A) The following technical interferences will increase the ESR result: vibrating surface, reading after 60 minutes, and tilting the sedimentation rate tube.
B) When plasma proteins increase, they cause the RBCs to stack together like poker chips, a condition known as rouleaux.
C) ESR tests cannot be performed on capillary blood because of the volume of blood needed.
D) The following medical conditions will cause a decreased ESR result: inflammatory diseases, autoimmune disorders, cancer, and leukemia.
D
4
Which of the following WBCs does not match the associated description?

A) Basophil becomes a mast cell when it enters the tissues to mediate the inflammatory response.
B) Lymphocyte is the smallest WBC.
C) Eosinophil increases in number during allergic reactions.
D) Neutrophil can differentiate into a T cell or B cell.
E) Monocyte is the largest WBC.
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5
Which of the following statements regarding hematocrits is false?

A) If capillary blood from a finger is used for the microhematocrit, the capillary tube must not contain an anticoagulant.
B) Spun hematocrits should be performed in duplicate, with results falling within 2% of each other.
C) Note the appearance of the plasma for hemolysis (red) and/or lipemia (cloudy white due to high fat content).
D) One condition in which a high hematocrit value might be found is polycythemia.
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6
The complete blood count (CBC) generally includes all of the following except:

A) hemoglobin.
B) hematocrit.
C) ESR.
D) RBC count.
E) WBC count.
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7
Hematology is the study of:

A) blood chemistry.
B) proteins in the blood.
C) blood plasma.
D) formed elements in the blood and bone marrow.
E) infectious diseases in the blood.
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8
Which term does not match its description?

A) Erythrocytes are the most numerous blood cells, occupying almost 50% of blood volume.
B) Bands are immature neutrophils.
C) Platelets are fragments of cytoplasm.
D) Segs are mature neutrophils.
E) Basophils have coarse red granules in their cytoplasm.
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9
Which of the following is not a granulocyte?

A) Eosinophil
B) Neutrophil
C) Lymphocyte
D) Basophil
E) Band/seg
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10
The major component in the erythrocyte that carries oxygen is:

A) hematocrit.
B) hemoglobin.
C) plasma.
D) protein.
E) iron.
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11
Which of the following statements regarding the making and staining of a blood smear is true?

A) When identifying cells, one should note the size, shape, and color of the blood cell, its nucleus, and its cytoplasm.
B) Blood cells are observed and identified under the low power lens of the microscope.
C) A properly done blood smear will have a blunt edge at the end of the smear and a thinner distribution of blood cells in the heel of the slide.
D) Medical assistants are qualified to read and report a stained blood smear.
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12
Most CLIA-waived hematology tests use blood from a(n):

A) artery.
B) vein.
C) capillary.
D) Vacutainer.
E) syringe.
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13
Which of the following is not a formed element in the blood?

A) Prothrombin
B) White blood cells (WBCs)
C) Red blood cells (RBCs)
D) Platelets
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14
A critical vitamin used by the liver to produce clotting factors is vitamin:

A) A.
B) D.
C) E.
D) B.
E) K.
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15
The anticoagulant and Vacutainer tube used for most hematology testing in a reference lab is:

A) heparin in a green-top tube.
B) heparin in a lavender-top tube.
C) ethylenediaminetetraacetic acid (EDTA) in a green-top tube.
D) EDTA in a lavender-top tube.
E) none of these; no anticoagulant is needed for hematology tests.
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16
Match between columns
Increase in WBCs (usually due to infection)
Mononucleosis
Increase in WBCs (usually due to infection)
ALL (acute lymphocytic leukemia)
Increase in WBCs (usually due to infection)
CML (chronic myelocytic leukemia)
Increase in WBCs (usually due to infection)
Leukocytosis
Increase in WBCs (usually due to infection)
Leukocytopenia
Presence of atypical "reactive" lymphocytes
Mononucleosis
Presence of atypical "reactive" lymphocytes
CML (chronic myelocytic leukemia)
Presence of atypical "reactive" lymphocytes
Leukocytosis
Presence of atypical "reactive" lymphocytes
Leukocytopenia
Presence of atypical "reactive" lymphocytes
Mononucleosis
Long-term cancer of granulocytes in bone marrow
CML (chronic myelocytic leukemia)
Long-term cancer of granulocytes in bone marrow
ALL (acute lymphocytic leukemia)
Long-term cancer of granulocytes in bone marrow
Leukocytosis
Long-term cancer of granulocytes in bone marrow
Leukocytopenia
Long-term cancer of granulocytes in bone marrow
Mononucleosis
Abnormal decrease of WBCs
Leukocytopenia
Abnormal decrease of WBCs
Leukocytosis
Abnormal decrease of WBCs
CML (chronic myelocytic leukemia)
Abnormal decrease of WBCs
ALL (acute lymphocytic leukemia)
Abnormal decrease of WBCs
ALL (acute lymphocytic leukemia)
Sudden cancer of a nongranulocyte
Mononucleosis
Sudden cancer of a nongranulocyte
Leukocytopenia
Sudden cancer of a nongranulocyte
Leukocytosis
Sudden cancer of a nongranulocyte
CML (chronic myelocytic leukemia)
Sudden cancer of a nongranulocyte
ALL (acute lymphocytic leukemia)
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17
Match between columns
Seen with blood loss (menses, ulcers, hemorrhaging)
Iron deficiency anemia
Seen with blood loss (menses, ulcers, hemorrhaging)
Hemolytic anemia
Seen with blood loss (menses, ulcers, hemorrhaging)
Sickle cell anemia
Seen with blood loss (menses, ulcers, hemorrhaging)
Pernicious anemia
Seen with blood loss (menses, ulcers, hemorrhaging)
Aplastic anemia
Inherited abnormal hemoglobin S
Iron deficiency anemia
Inherited abnormal hemoglobin S
Hemolytic anemia
Inherited abnormal hemoglobin S
Sickle cell anemia
Inherited abnormal hemoglobin S
Pernicious anemia
Inherited abnormal hemoglobin S
Aplastic anemia
Destruction of stem cells in bone marrow from toxins
Iron deficiency anemia
Destruction of stem cells in bone marrow from toxins
Hemolytic anemia
Destruction of stem cells in bone marrow from toxins
Sickle cell anemia
Destruction of stem cells in bone marrow from toxins
Pernicious anemia
Destruction of stem cells in bone marrow from toxins
Aplastic anemia
Caused by decreased vitamin B12
Iron deficiency anemia
Caused by decreased vitamin B12
Hemolytic anemia
Caused by decreased vitamin B12
Sickle cell anemia
Caused by decreased vitamin B12
Pernicious anemia
Caused by decreased vitamin B12
Aplastic anemia
Destruction of circulating RBCs
Iron deficiency anemia
Destruction of circulating RBCs
Hemolytic anemia
Destruction of circulating RBCs
Sickle cell anemia
Destruction of circulating RBCs
Pernicious anemia
Destruction of circulating RBCs
Aplastic anemia
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MCH (mean cell hemoglobin)
Hgb/HCT (31% to37% or g/dL)
MCH (mean cell hemoglobin)
Hgb/RBC (26 to34 pg)
MCH (mean cell hemoglobin)
Hgb/HCT (31% to37% or g/dL)
MCHC (mean cell hemoglobin concentration)
HCT/RBC (82 to98 micrometers/fL)
MCHC (mean cell hemoglobin concentration)
Hgb/RBC (26 to34 pg)
MCHC (mean cell hemoglobin concentration)
HCT/RBC (82 to98 micrometers/fL)
MCV (mean cell volume)
Hgb/HCT (31% to37% or g/dL)
MCV (mean cell volume)
Hgb/RBC (26 to34 pg)
MCV (mean cell volume)
HCT/RBC (82 to98 micrometers/fL)
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Abnormal decrease in RBCs
Leukopenia
Abnormal decrease in RBCs
Anemia
Abnormal decrease in RBCs
Leukemia
Abnormal decrease in RBCs
Leukocytosis
Abnormal decrease in RBCs
Polycythemia
Cancer of the WBCs
Anemia
Cancer of the WBCs
Leukopenia
Cancer of the WBCs
Leukemia
Cancer of the WBCs
Leukocytosis
Cancer of the WBCs
Polycythemia
Abnormal increase in WBCs
Anemia
Abnormal increase in WBCs
Leukopenia
Abnormal increase in WBCs
Leukemia
Abnormal increase in WBCs
Leukocytosis
Abnormal increase in WBCs
Polycythemia
Abnormal decrease in WBCs
Anemia
Abnormal decrease in WBCs
Leukopenia
Abnormal decrease in WBCs
Leukemia
Abnormal decrease in WBCs
Leukocytosis
Abnormal decrease in WBCs
Polycythemia
Abnormal increase in RBCs
Anemia
Abnormal increase in RBCs
Leukopenia
Abnormal increase in RBCs
Leukemia
Abnormal increase in RBCs
Leukocytosis
Abnormal increase in RBCs
Polycythemia
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HemoCue
Hematocrit (HCT)
HemoCue
Sedimentation rate
HemoCue
Coagulation test
HemoCue
Hemoglobin (Hgb)
HemoCue
CBC
Sediplast/Westergren/Streck
Hematocrit (HCT)
Sediplast/Westergren/Streck
Sedimentation rate
Sediplast/Westergren/Streck
Coagulation test
Sediplast/Westergren/Streck
Hemoglobin (Hgb)
Sediplast/Westergren/Streck
CBC
HemataSTAT
CBC
HemataSTAT
Hemoglobin (Hgb)
HemataSTAT
Coagulation test
HemataSTAT
Sedimentation rate
HemataSTAT
Hematocrit (HCT)
QBC
Sedimentation rate
QBC
Coagulation test
QBC
Hemoglobin (Hgb)
QBC
CBC
QBC
Hematocrit (HCT)
Pro time
Hematocrit (HCT)
Pro time
Sedimentation rate
Pro time
Coagulation test
Pro time
Hemoglobin (Hgb)
Pro time
CBC
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Pro time
36% to55%
Pro time
12 to18 g/dL
Pro time
36% to55%
Pro time
0 to20 mm/hour
ESR
1.0 INR
ESR
12 to18 g/dL
ESR
0 to20 mm/hour
ESR
1.0 INR
Hemoglobin
12 to18 g/dL
Hemoglobin
36% to55%
Hemoglobin
0 to20 mm/hour
Hemoglobin
1.0 INR
Hematocrit
12 to18 g/dL
Hematocrit
36% to55%
Hematocrit
0 to20 mm/hour
Hematocrit
1.0 INR
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RBC layer
Label C
RBC layer
Label C
RBC layer
Label B
RBC layer
Label D
RBC layer
Label E
Air
Label A
Air
Label C
Air
Label B
Air
Label D
Air
Label E
Buffy layer
Label A
Buffy layer
Label C
Buffy layer
Label B
Buffy layer
Label D
Buffy layer
Label E
Clay sealant
Label A
Clay sealant
Label C
Clay sealant
Label B
Clay sealant
Label D
Clay sealant
Label E
Plasma
Label A
Plasma
Label B
Plasma
Label D
Plasma
Label E
Plasma
Label A
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A byproduct of RBC breakdown that is sent to the liver
Anemia
A byproduct of RBC breakdown that is sent to the liver
Heme
A byproduct of RBC breakdown that is sent to the liver
Globin
A byproduct of RBC breakdown that is sent to the liver
Bilirubin
A byproduct of RBC breakdown that is sent to the liver
Hemoglobin
The protein portion of the hemoglobin molecule
Hemoglobin
The protein portion of the hemoglobin molecule
Bilirubin
The protein portion of the hemoglobin molecule
Globin
The protein portion of the hemoglobin molecule
Heme
The protein portion of the hemoglobin molecule
Anemia
The iron portion of the hemoglobin molecule
Hemoglobin
The iron portion of the hemoglobin molecule
Bilirubin
The iron portion of the hemoglobin molecule
Anemia
The iron portion of the hemoglobin molecule
Globin
The iron portion of the hemoglobin molecule
Heme
A condition in which the RBC or hemoglobin levels are below normal
Anemia
A condition in which the RBC or hemoglobin levels are below normal
Hemoglobin
A condition in which the RBC or hemoglobin levels are below normal
Bilirubin
A condition in which the RBC or hemoglobin levels are below normal
Globin
A condition in which the RBC or hemoglobin levels are below normal
Heme
A molecule that has a reddish pigment and is capable of carrying oxygen
Anemia
A molecule that has a reddish pigment and is capable of carrying oxygen
Hemoglobin
A molecule that has a reddish pigment and is capable of carrying oxygen
Bilirubin
A molecule that has a reddish pigment and is capable of carrying oxygen
Globin
A molecule that has a reddish pigment and is capable of carrying oxygen
Heme
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Activates prothrombin to become thrombin
Thrombin
Activates prothrombin to become thrombin
Thromboplastin
Activates prothrombin to become thrombin
Fibrin
Activates prothrombin to become thrombin
Thrombin
Activates prothrombin to become thrombin
Heparin
A natural anticoagulant that prevents excessive clotting
Embolus
A natural anticoagulant that prevents excessive clotting
Thromboplastin
A natural anticoagulant that prevents excessive clotting
Fibrin
A natural anticoagulant that prevents excessive clotting
Heparin
A natural anticoagulant that prevents excessive clotting
Embolus
The final sticky, stringy product of coagulation
Thromboplastin
The final sticky, stringy product of coagulation
Fibrin
The final sticky, stringy product of coagulation
Thrombin
The final sticky, stringy product of coagulation
Heparin
The final sticky, stringy product of coagulation
Embolus
Activates fibrinogen to become fibrin
Thromboplastin
Activates fibrinogen to become fibrin
Fibrin
Activates fibrinogen to become fibrin
Thrombin
Activates fibrinogen to become fibrin
Heparin
Activates fibrinogen to become fibrin
Embolus
A moving clot
Thromboplastin
A moving clot
Fibrin
A moving clot
Thrombin
A moving clot
Heparin
A moving clot
Embolus
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Many-shaped nucleus or "seg"
Nongranulocytes
Many-shaped nucleus or "seg"
Myeloblast
Many-shaped nucleus or "seg"
Megakaryocyte
Many-shaped nucleus or "seg"
Macrophages
Many-shaped nucleus or "seg"
Nongranulocytes
Lymphocyte and monocyte group
Polymorphonuclear
Lymphocyte and monocyte group
Myeloblast
Lymphocyte and monocyte group
Megakaryocyte
Lymphocyte and monocyte group
Macrophages
Lymphocyte and monocyte group
Nongranulocytes
Large nuclear cell in the bone marrow that fragments its cytoplasm to become platelets
Polymorphonuclear
Large nuclear cell in the bone marrow that fragments its cytoplasm to become platelets
Myeloblast
Large nuclear cell in the bone marrow that fragments its cytoplasm to become platelets
Megakaryocyte
Large nuclear cell in the bone marrow that fragments its cytoplasm to become platelets
Macrophages
Large nuclear cell in the bone marrow that fragments its cytoplasm to become platelets
Polymorphonuclear
WBC stem cell that develops into the three kinds of granulocytes
Myeloblast
WBC stem cell that develops into the three kinds of granulocytes
Megakaryocyte
WBC stem cell that develops into the three kinds of granulocytes
Macrophages
WBC stem cell that develops into the three kinds of granulocytes
Nongranulocytes
WBC stem cell that develops into the three kinds of granulocytes
Polymorphonuclear
Large engulfing cells in the tissues that came from monocytes
Myeloblast
Large engulfing cells in the tissues that came from monocytes
Megakaryocyte
Large engulfing cells in the tissues that came from monocytes
Macrophages
Large engulfing cells in the tissues that came from monocytes
Nongranulocytes
Large engulfing cells in the tissues that came from monocytes
Polymorphonuclear
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Newly released RBCs into the blood that still contain some nuclear DNA
Anisocytosis
Newly released RBCs into the blood that still contain some nuclear DNA
Reticulocytes
Newly released RBCs into the blood that still contain some nuclear DNA
Poikilocytosis
Newly released RBCs into the blood that still contain some nuclear DNA
Hematologists
Newly released RBCs into the blood that still contain some nuclear DNA
Erythroblast
Immature red cell in bone marrow (also called rubriblast)
Anisocytosis
Immature red cell in bone marrow (also called rubriblast)
Reticulocytes
Immature red cell in bone marrow (also called rubriblast)
Poikilocytosis
Immature red cell in bone marrow (also called rubriblast)
Hematologists
Immature red cell in bone marrow (also called rubriblast)
Erythroblast
Variances in RBC size
Anisocytosis
Variances in RBC size
Reticulocytes
Variances in RBC size
Poikilocytosis
Variances in RBC size
Erythroblast
Variances in RBC size
Hematologists
Abnormally shaped
Erythroblast
Abnormally shaped
Anisocytosis
Abnormally shaped
Reticulocytes
Abnormally shaped
Poikilocytosis
Abnormally shaped
Hematologists
Specialists who evaluate the cellular elements of blood microscopically and analytically
Erythroblast
Specialists who evaluate the cellular elements of blood microscopically and analytically
Anisocytosis
Specialists who evaluate the cellular elements of blood microscopically and analytically
Reticulocytes
Specialists who evaluate the cellular elements of blood microscopically and analytically
Poikilocytosis
Specialists who evaluate the cellular elements of blood microscopically and analytically
Hematologists
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