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WorksheetsHEMA 1 FINAL EXAM
Total questions: 100
Worksheet time: 58mins
Which of the following cells is considered pathognomonic for Hodgkin’s disease?
Niemann-Pick cells
Reactive lymphocytes
Flame cells
Reed-Sternberg cells
In which of the following conditions does LAP show the least activity?
Leukomoid reactions
IMF
PV
Chronic Myelogenous Leukemia
What is the anticoagulant of choice for coagulation studies?
EDTA
Sodium fluoride
Sodium citrate
Acid citrate dextrose
Which of the following does not characterize anemia of chronic disease?
Decreased serum iron
Increased ferritin
Decreased % saturation
Increased TIBC
With what leukemia is disseminated intravascular coagulation associated?
M1
M3
M6
CML
The characteristic cell found to be increased in infectious mononucleosis is
Eosinophil
Variant lymphocyte
Monocyte
Neutrophil
The following are compounds formed in the synthesis of heme:
1. coproporphyrin
2. porphobilinogen
3. urophorphyrinogen
4. protoporphyrinogen
Which of the following responses lists these compounds in the order in which they are formed?
4, 3, 2,1
2, 3, 1, 4
4, 2, 3, 1
2, 1, 3,4
The majority of the iron in an adult is found as a constituent of:
hemoglobin
hemosiderin
myoglobin
transferrin
The main function of the hexose monophosphate shunt in the erythrocyte is:
regulate the level of 2,3 DPG
Provide reduced glutathione to prevent oxidation of hemoglobin
Prevent the reduction of heme iron
provide energy for membrane maintenance
In order for hemoglobin to combine reversibly with oxygen, the iron must be:
complexed with haptoglobulin
freely circulating in the cytoplasm
attached to transferrin
in the ferrous state
In which of the following disease states are teardrops cells and abnormal platelets most characteristically seen?
hemolytic anemia
multiple myeloma
G6PD deficiency
Myeloid Metaplasia
The characteristic erythrocyte found in pernicious anemia
microcytic
spherocytic
hypochromic
macrocytic
Platelet originates in the bone marrow from:
Megaloblasts
Myeloblasts
Macrophages
Monocytes
Megakaryocytes
RBC inclusion body seen in megaloblastic anemia:
Basophilic stipplings
Howell Jolly bodies
Hemoglobin H inclusion bodies
Heinz bodies
Red blood cell inclusions are removed without destroying the cell itself by the:
Liver
Spleen
Kidney
Bone marrow
Hemoglobin Bart’s is composed of
Four alpha chains
Four beta chains
Four gamma chains
Two alpha and tow gamma chains
Which of the following is characteristically seen in abetalipoproteinemia?
Discocytes
Acanthocytes
Stomatocytes
Codocytes
Spherocytes
Plasma from a patient with lupus coagulation inhibitor (lupus anticoagulant) can show:
a prolonged APTT and normal PT
may exhibit bleeding tendencies
no change with platelet neutralization
complete correction when incubated with normal plasma
A patient is diagnosed as having bacterial septicemia. Which of the following would best describe the expected change in his peripheral blood?
granulocytic leukemoid reaction
lymphocytic leukemoid reaction
neutropenia
eosinophilia
Which of the following stains is most frequently used to differentiate acute myelocytic (AML) from acute lymphocytic leukemia (ALL)?
alkaline phosphatase
nonspecific esterase
acid phosphatase
peroxidase
Which of the following stains is helpful in the diagnosis of suspected erythroleukemia?
peroxidase
nonspecific esterase
periodic acid-Schiff (PAS)
acid phosphatase
Of the following, the disease most closely associated with pale blue inclusions in granulocytes and giant platelets is:
Gaucher's disease
Alder-Reilly anomaly
May-Hegglin anomaly
Pelger-Huet anomaly
A patient has a congenital nonspherocytic hemolytic anemia. After exposure to antimalarial drugs, the patient experiences a severe hemolytic episode. This episode is characterized by red cell inclusions caused by hemoglobin denaturation. Which of the following conditions is most consistent with these findings?
G-6-PD deficiency
thalassemia major
pyruvate kinase deficiency
paroxysmal nocturnal hemoglobinuria
A useful chemical test for the diagnosis of hairy-cell leukemia is the:
peroxidase test
Sudan black B test
periodic acid-Schiff test
tartrate-resistant acid phosphatase test
Which of the following bone marrow findings favors the diagnosis of multiple myeloma?
presence of Reed-Sternberg cells
sheaths of immature plasma cells
presence of flame cells and Russell bodies
presence of plasmacytic satellitosis
The Philadelphia chromosome is formed by a translocation between the:
long arm of chromosome 22 and long arm of chromosome 9
long arm of chromosome 21 and long arm of chromosome 9
long arm of chromosome 21 and short arm of chromosome 6
long arm of chromosome 22 and short arm of chromosome 6
In normal adult bone marrow, the most common granulocyte is the:
basophil
myeloblast
eosinophil
metamyelocyte
Heparin acts by:
precipitating calcium
binding calcium
activating plasmin
inhibiting thrombin
Supravital staining is important for reticulocytes since the cells must be living in order to stain the:
remaining RNA in the cell
iron before it precipitates
cell membrane before it dries out
denatured hemoglobin in the cell
Most childhood leukemias are:
acute lymphocytic
acute monocytic
chronic myelocytic
chronic lymphocytic
Contains lithium heparin as anticoagulant:
blue top
pink top
gray top
green top
Three methods of venipuncture except:
arterial
ETS
syringe
butterfly
Which of the following is NOT a characteristic of the Brachial Artery?
It has pulse
The wall is thicker than a vein
The blood is bright red
It is preferred for venipuncture
Which of the following may result in the hemolysis of blood?
Using a needle with too small a lumen
Removing the needle before the tourniquet
Storing the tube at room temperature
Allowing the tube to fill to the exhaustion of the vacuum
Leaving a tourniquet on for too long can cause what complication?
Syncope
Hematoma
Hemolysis
Hemoconcentration
Shaking a tube rather than inverting it, can cause what complication?
Syncope
Hematoma
Hemolysis
Hemoconcentration
Thalassemias are characterized by:
structural abnormalities in the hemoglobin molecule
absence of iron in hemoglobin
decreased rate of heme synthesis
decreased rate of globin synthesis
Which of the following is associated with Chediak-Higashi syndrome?
membrane defect of lysosomes
Dohle bodies and giant platelets
two-lobed neutrophils
mucopolysaccharidosis
Morphologic variants of plasma cells do NOT include:
flame cells
morula cells
grape cells
Gaucher's cells
Which of the following cell types is characteristic of Pelger Huet anomaly?
band form
pince-nez form
normal neutrophil
myelocyte
Which of the following is the formula for mean corpuscular volume (MCV)?
(Hgb x 10)/RBC
Hgb/Hct
(Hct x 10)/RBC
RBC/Hct
Which of the following characteristics are common to hereditary spherocytosis, hereditary elliptocytosis, hereditary stomatocytosis, and paroxysmal nocturnal hemoglobinuria?
autosomal dominant inheritance
red cell membrane defects
positive direct antiglobulin test
measured platelet count
Which is the first stage of erythrocytic maturation in which the cytoplasm is pink due to the formation of hemoglobin?
Reticulocyte
Pronormoblast
Basophilic normoblast
Polychromatic normoblast
Which is the major Hgb found in the RBCs of patients with sickle cell trait?
Hgb S
Hgb F
Hgb A2
Hgb A1
Which antibiotic(s) is (are) most often implicated in the development of aplastic anemia
Sulfonamides
Penicillin
Tetracycline
Chloramphenicol
It is a sample of known quantity and are prepared from the same matrix as patient specimens and are sampled alongside patient specimens to accomplish within-run assay validation.
Calibrators
Standard
Controls
Blank reagent
When controls are run, they must fall within predetermined dispersal limits, typically at ________________.
+1SD
+2SD
+3SD
+4SD
It is a measure of the smallest increment/amount of the analyte that can be distinguished by the assay.
Accuracy
Precision
Specificity
Sensitivity
At what hematopoietic stage does Hgb F produced?
Hepatic Stage
Mesoblastic Stage
Myeloid Stage
Medullary Stage
It is the reference method for hemoglobin assay that is performed manually but has been adapted to automated instruments.
Alkaline Agar Electrophoresis
Citrate Agar Electrophoresis
Cyanmethemoglbin method
Copper Sulfate Method
Which granulocyte maturation stage does secondary granules occurs?
Myeloblast
Myelocyte
Promyelocyte
Metamyelocyte
It is a group of disorder characterized by iron loading and its accumulation in the mitochondria of erythroid precursors due to a defect in the heme synthesis.
Anemia of chronic disease
Thalassemia
Sideroblastic Anemia
Iron deficiency Anemia
The earliest granulocytic stage in the myeloid series capable of mitosis is:
Myeloblast
Metamyelocyte
Promyelocyte
Band cell
Myelocyte
The earliest stage in the myeloid series at which it is possible to classify a given cell
Myeloblast
Metamyelocyte
Promyelocyte
Band
Myelocyte
The earliest stage in the myeloid series to appear normally in the peripheral blood is the:
Myeloblast
Metamyelocyte
Promyelocyte
Band cell
Myelocyte
An extremely high speed centrifuge able to reach very high RCF values:
Horizontal head centrifuge
Angle head centrifuge
Ultracentrifuge
All of the given choices
Dilution for the RBC count in automated counting instruments:
1:5
1:250
1:2,500
1:50,000
Three values are counted directly on electronic impedance instruments
RBCs, WBCs, and platelets
RBCs, WBCs, and hemoglobin
RBCs, RDW, and MCV
Hematocrit
The correct sequence(s) of events in successful phagocytosis is (are)
chemotaxis, opsonization, phagosome formation, and the action of antibacterial substances
opsonization, chemotaxis, phagosome formation, and the action of antibacterial substances
engulfment, opsonization, digestion, and destruction of bacteria or particulate matter
None of the given choices
The incidence of leukemia is higher in
Scandinavian versus Japanese populations
American blacks versus American whites
chronic forms in children versus chronic forms in adults
acute forms in older adults versus acute forms in children
Which of the following is the correct maturation series of T lymphocyte?
Plasmablast, Proplasmacyte, Plasma cell
Proplasmacyte, Plasma cell, Plasmablast,
Lymphoblast, Prolymphocyte, Mature lymphocyte
Prolymphocyte, Lymphoblast, Mature lymphocyte
Which of the following is the correct maturation series of B lymphocyte?
Plasmablast, Proplasmacyte, Plasma cell
Proplasmacyte, Plasma cell, Plasmablast,
Lymphoblast, Prolymphocyte, Mature lymphocyte
Prolymphocyte, Lymphoblast, Mature lymphocyte
Associated with DIC.
M1
M2
M3
M4
M5
Spherocytes
Short, scalloped, or spike-like projections that are regularly distributed around the cell
Fragments of erythrocytes
The scooped-out part of an erythrocyte that remains after a blister cell ruptures
Compact round shape
Pappenheimer bodies
Nuclear remnants of DNA
Precipitated denatured hemoglobin
Granules composed of ribosomes and RNA
Aggregates of iron, mitochondria, and ribosomes near the red cell periphery as purple dots.
Auer rods may be seen in all of the following except:
Acute myelomonocytic leukemia (M4)
Acute lymphoblastic leukemia
Acute myeloid leukemia without maturation (M1)
Acute promyelocytic leukemia (M3)
Which type of anemia is usually present in a patient with acute leukemia?
Microcytic, hyperchromic
Microcytic, hypochromic
Normocytic, normochromic
Macrocytic, normochromic
In which age group does acute lymphoblastic leukemia occur with the highest frequency?
1–15 years
20–35 years
45–60 years
60–75 years
Muramidase (lysozyme) is present in:
granulocytes and their precursors
monocytes and their precursors
granulocytes, monocytes, and their precursors
lymphocytes and their precursors
In an electronic or laser particle cell counter, clumped platelets may interfere with which of the following parameters?
white blood cell count
red blood cell count
hemoglobin
hematocrit
Blood collected in EDTA undergoes which of the following changes if kept at room temperature for 6-24 hours?
increased hematocrit and MCV
increased ESR and MCV
increased MCHC and MCV
decreased reticulocyte count and hematocrit
Decreased to normal erythropoietin production is most likely to be associated with:
polycythemia Vera
polycythemia, secondary to hypoxia
relative polycythemia associated with dehydration
polycythemia associated with renal disease
Multiple myeloma is generally characterized by:
plasmacytic satellitosis in the bone marrow
many plasma cells in the peripheral blood
many Mott cells in the peripheral blood
rouleaux formation
Of the following, the disease most closely associated with granulocyte hyposegmentation is:
May-Hegglin anomaly
Pelger-Huet anomaly
Chediak-Higashi syndrome
Gaucher's disease
Erythropoietin acts to:
shorten the replication time of the granulocytes
stimulate RNA synthesis of erythroid cells
increase colony-stimulating factors produced by the B-lymphocytes
decrease the release of marrow reticulocytes
Which of the following is associated with Chediak-Higashi syndrome?
membrane defect of lysosomes
Dohle bodies and giant platelets
two-lobed neutrophils
mucopolysaccharidosis
Which of the following describes the process known as culling?
Release of red cells from the bone marrow
Binding of free hemoglobin by transport proteins
Incorporation of iron into protoporphyrin IX
Removal of abnormal red cells by the spleen
Hemoglobin forms that are incapable of oxygen transport include
Deoxyhemoglobin and oxyhemoglobin
Oxyhemoglobin and carboxyhemoglobin
Carboxyhemoglobin and methemoglobin
Methemoglobin and deoxyhemoglobin
The Na+-K+ cation pump is an important mechanism in keeping the red blood cell intact. Its function is to maintain a high level of
Intracellular Na+
Intracellular K+
Plasma Na+
Plasma K+
When spherocytes are reported, what is observed on the peripheral blood smear?
Red cells without a central pallor
Red cells with blunt projections
Red cells with sharp projections
Red cells with intracellular rod-shaped crystals
Which of the following factors will result in an immediate increase in oxygen delivery to the tissues?
Increased pH
High altitudes
Increased hemoglobin binding of 2,3-BPG
Increased renal release of erythropoietin
The major storage form of iron is
Ferritin
Transferrin
Hemosiderin
Hemachromatin
Which protein is primarily responsible for transport of hemoglobin dimers resulting from intravascular hemolysis?
Hemopexin
Albumin
Hemosiderin
Haptoglobin
A patient with normocytic, normochromic anemia secondary to small cell carcinoma may be exhibiting an anemia designated a
Hemolytic
Megaloblastic
Myelopthisic
Sideroblastic
Which of the following is the most appropriate treatment for sickle cell anemia?
Hydroxyurea
Supportive therapy
Hyperbaric oxygen
Iron
In children, the most important effect of lead poisoning is on the
Liver
Kidney
Neurologic system
Development of erythrocytes
An increase in erythropoietin is not a normal compensating mechanism in which of the following conditions?
Renal tumors
Heavy smoking
Cardiovascular disease
Pulmonary disease
Which of the following factors is not associated with variations in the total white blood cell count?
Age
Exercise
Emotional stress
Sex
The presence of both immature neutrophils and nucleated erythrocytes in the peripheral blood is most accurately called a
Neutrophilic left shift
Regenerative left shift
Neutrophilic leukemoid reaction
Leukoerythroblastic reaction
In which of the following are eosinophils not increased?
Cushing Syndrome
Allergic Disorders
Skin Disorders
Parasitic Infection
Which of the following is not commonly found in acute myelogenous leukemias?
Neutropenia
Thrombocytopenia
Hepatosplenomegaly
Lymphadenopathy
A Gaucher cell is best described as a macrophage with
"Wrinkled" cytoplasm due to an accumulation of glucocerebroside
"Foamy" cytoplasm filled with unmetabolized sphingomyelin
Pronounced vacuolization and deposits of cholesterol
Abundant cytoplasm containing storage iron and cellular remnants
The presence of the chromosomal abnormality t(15;17) and a high incidence of disseminated intravascular coagulation (DIG) is diagnostic of
Acute myeloblastic leukemia without maturation (FAB type Ml)
Acute myeloblastic leukemia with maturation (FAB type M2)
Acute promyelocytic leukemia (FAB type M3)
Acute myelomonocytic leukemia (FAB type M4)
Which of the following gene mutations correlates with the t(9;22) that is present in Philadelphia chromosome positive chronic myelogenous leukemia?
MYC/IGH
BCR/ABL
PML/RARA
JAK2
What is the key diagnostic test for Hodgkin lymphoma?
Bone marrow biopsy
Lymph node biopsy
Spinal tap
Skin biopsy
What combination of reagents is used to measure hemoglobin?
Hydrochloric acid and p-dimethyl-aminobenzaldehyde
Potassium ferricyanide and potassium cyanide
Sodium bisulfite and sodium metabisulfite
Sodium citrate and hydrogen peroxide
The slowest-moving hemoglobin(s) on an alkaline electrophoresis at pH 8.6 is(are)
A
A2, C,E, andO
F
S, D, andG
The components of Wright's stain include
Crystal violet and safranin
Brilliant green and neutral red
New methylene blue and carbolfuchsin
Methylene blue and eosin
What is the principle of automated impedance cell counters?
Angle of laser beam scatter by cells
Amplification of an electrical current by cells
Interruption of an electrical current by cells
Change in optical density of the solution containing cell
Side angle scatter in a laser-based cell counting system is used to measure
Cell size
Cytoplasmic granularity
Cell number
Immunologic (antigenic) identification
