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WorksheetsHEMATOLOGY ASSESSMENT EXAM SEMINAR 1&2
Total questions: 110
Worksheet time: 1hrs 8mins
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
Teardrop shaped RBC’s
Megalocyte
Elliptocyte
Dacryocyte
Drepanocyte
Codocyte
Target cells
Megalocyte
Elliptocyte
Dacryocyte
Drepanocyte
Codocyte
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
The Prussian blue staining of peripheral blood identifies:
Howell-Jolly bodies
siderotic granules
reticulocytes
basophilic stippling
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
The combination of increased capillary fragility and prolonged bleeding time suggests a deficiency in
thromboplastin
prothrombin
platelets
fibrinogen
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
Aspirin affects platelet function by interfering with platelets' metabolism of:
prostaglandins
lipids
carbohydrates
nucleic acids
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
Leukocyte alkaline phosphatase activity is decreased in:
acute infections
pregnant women
polycythemia Vera
paroxysmal nocturnal hemoglobinuria
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
Which of the following stains is used to demonstrate iron, ferritin, and hemosiderin?
peroxidase
Sudan black B
periodic acid-Schiff (PAS)
Prussian blue
Which of the following may be used to stain glycogen, polysaccharides, and glycoproteins?
peroxidase
Sudan black B
periodic acid-Schiff (PAS)
nitroblue tetrazolium (NBT)
Which of the following cells is the largest cell in the bone marrow:
megakaryocyte
histiocyte
osteoblast
monocytes
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
The most likely cause of the macrocytosis that often accompanies anemia of myelofibrosis is:
folic acid deficiency
increased reticulocyte count
inadequate B12 absorption
pyridoxine deficiency
A hypercellular marrow with an M:E ratio of 6:l is most commonly due to:
lymphoid hyperplasia
granulocytic hyperplasia
normoblastic hyperplasia
myeloid hypoplasia
In normal adult bone marrow, the most common granulocyte is the:
basophil
myeloblast
eosinophil
metamyelocyte
Megaloblastic asynchronous development in the bone marrow indicates which one of the following?
proliferation of erythrocyte precursors
impaired synthesis of DNA
inadequate production of erythropoietin
deficiency of G-6-PD
Which of the following platelet responses is most likely associated with hemophilia A (Factor VIII deficiency)?
defective ADP release; normal response to ADP
decreased amount of ADP in platelets
absent aggregation to epinephrine, ADP, and collagen
normal platelet aggregation
Giant, bizarre-shaped, multinucleated erythroid precursors are present in which of the following
chronic granulocytic leukemia
myelofibrosis with myeloid metaplasia
erythroleukemia
acute granulocytic leukemia
Terminal deoxynucleotidyl transferase (TdT) is a marker found on:
hairy cells
myeloblasts
monoblasts
lymphoblasts
The M:E ratio in chronic granulocytic leukemia is usually:
normal
high
low
variable
The characteristic morphologic feature in lead poisoning is:
macrocytosis
target cells (codocytes)
basophilic stippling
rouleaux formation
The morphologic feature most characteristic of hemolytic anemia is
spherocytosis
rouleaux formation
basophilic stippling
target cells
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
Prothrombin is
a protein formed by the liver in the presence of vitamin K
an enzyme that converts fibrinogen into fibrin threads
the end product of the reaction between fibrinogen and thrombin
a protein released by platelets during coagulation
Which of the following coagulation factors is considered to be labile?
II
V
VII
X
A coagulation factor synthesized in the liver and vitamin K dependent is:
I
II
VIII
XIII
Which of the following factors is used only in the extrinsic coagulation pathway?
II
V
VII
VIII
What cell shape is MOST commonly associated with an increased MCHC?
teardrop cells
target cells
spherocytes
sickle cells
Contains Sodium fluoride:
pink top
blue top
gray top
green top
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
The anemia of chronic infection is characterized by:
decreased iron stores in the reticuloendothelial system
decreased serum iron levels
macrocytic erythrocytes
increased serum iron-binding capacity
Which of the following is associated with Chediak-Higashi syndrome?
membrane defect of lysosomes
Dohle bodies and giant platelets
two-lobed neutrophils
mucopolysaccharidosis
Patients with chronic granulomatous disease suffer from frequent pyogenic infections owing to the inability of:
lymphocytes to produce bacterial antibodies
eosinophils to degranulate in the presence of bacteria
neutrophils to kill phagocytized bacteria
basophils to release histamine in the presence of bacteria
Which of the following is most closely associated with iron deficiency anemia?
iron overload in tissue
target cells
basophilic stippling
chronic blood loss
Auer rods are:
a normal aggregation of lysosomes or primary (azurophilic) granules
predominantly found in acute myelogenous leukemia
peroxidase negative
alkaline phosphatase positive
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
The ideal capillary blood collection site on a newborn is
tip of the thumb
ear lobe
plantar surface of the heel
the great toe
Of the following, the disease most closely associated with glucocerebrosidase deficiency is:
Gaucher's disease
Chediak-Higashi syndrome
Pelger-Huet anomaly
May-Hegglin anomaly
Of the following, the disease most closely associated with cytoplasmic granule fusion is:
Chediak-Higashi syndrome
Pelger-Huet anomaly
May-Hegglin anomaly
Alder-Reilly anomaly
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
Variation in red cell size observed on the peripheral smear is described as:
Anisocytosis
Hypochromia
Poikilocytosis
Pleocytosis
Which of the following erythrocyte inclusions can be visualized with supravital stain but cannot be detected on a Wright’s-stained blood smear?
Basophilic stippling
Heinz bodies
Howell–Jolly bodies
Siderotic granules
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 of the following can shift the hemoglobin oxygen dissociation curve to the right?
Increases in 2,3 DPG
Acidosis
Hypoxia
All of these options
Which is the major Hgb found in the RBCs of patients with sickle cell trait?
Hgb S
Hgb F
Hgb A2
Hgb A1
The morphological classification of anemias is based on which of the following?
M:E (myeloid:erythroid) ratio
Prussian blue stain
RBC indices
Reticulocyte count
Which antibiotic(s) is (are) most often implicated in the development of aplastic anemia
Sulfonamides
Penicillin
Tetracycline
Chloramphenicol
Iron deficiency anemia is characterized by
Decreased plasma iron, decreased % saturation, increased total iron-binding capacity (TIBC)
Decreased plasma iron, decreased plasma ferritin, normal RBC porphyrin
Decreased plasma iron, decreased % saturation, decreased TIBC
Decreased plasma iron, increased % saturation, decreased TIBC
Which morphological classification is characteristic of megaloblastic anemia?
Normocytic, normochromic
Microcytic, normochromic
Macrocytic, hypochromic
Macrocytic, normochromic
Components of quality assurance/assessment programs includes all of the following except?
Preexamination variables
Examination variables
Post examination variables
None of the given choices
Which of the following is not included in the examination/analytical phase of testing?
laboratory staff competence
assay and instrument selection
accuracy in transcription and filing of results
external and internal quality control
assay validation
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
These are materials used to adjust instrument accuracy by configuring an instrument to provide a result for a sample within an acceptable range.
Calibrators
Standard
Controls
Blank reagent
It is a measure of the smallest increment/amount of the analyte that can be distinguished by the assay.
Accuracy
Precision
Specificity
Sensitivity
Cells that is produced as early as mesoblastic stage of hematopoiesis.
Erythrocytes
Lymphocytes
Monocytes
Granuloytes
Megakaryocytes
At what hematopoietic stage does Hgb F produced?
Hepatic Stage
Mesoblastic Stage
Myeloid Stage
Medullary Stage
Which hemoglobin contains 2 alpha chains and 2 delta chains.
HgB A1
Hgb A2
Hgb F
Hgb A1c
This is considered the first human hematopoietic growth factor to be identified.
Thrombopoietin
Erythropoietin
Progesterone
Growth Hormone
Which of the following statement is incorrect as RBC matures?
The overall diameter of the cell decreases cytoplasm changes from blue to salmon pink.
The diameter of the nucleus decreases more rapidly and the size of the cell. As a result, the N:C ratio also decreases
The nuclear chromatin pattern becomes coarser, clumped, and condensed as RBC matures.
Nucleoli remains until the RBC matures and released in the bloodstream.
Which of the following is incorrectly paired:
Pronormoblasts aka Rubriblasts
Basophilic Normoblasts aka Prorubricyte
Polychromatophilic Normoblast aka Rubricyte
Orthochromic normoblast aka Polychromatophilic erythrocyte
Reticulcyte aka Diffusely Basophilic Erythrocyte
Which of the following is incorrectly paired:
Pronormoblasts aka Rubriblasts
Basophilic Normoblasts aka Prorubricyte
Polychromatophilic Normoblast aka Rubricyte
Orthochromic normoblast aka Polychromatophilic erythrocyte
Reticulcyte aka Diffusely Basophilic Erythrocyte
Which of the following RBC maturation stage does hemoglobin first appear?
Rubricyte
Metarubricyte
Reticulocyte
Rubriblasts
This pathway of RBC metabolism is the aerobic pathway.
Pentose phosphate pathway
Embden Meyerhoff Pathway
Rapoprt-Luebering Pathway
Methemoglobin Pathway
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 of the following is incorrect regarding anemia?
Anemia refers to the decrease in the oxygen carrying capacity of the blood which can arise if there is insufficient hemoglobin or the hemoglobin has impaired function.
Anemia is operationally defined as the reduction in the hemoglobin content of blood that can be caused by a decrease in RBCs, hemoglobin, and hematocrit below the reference interval for healthy individuals of similar age, sex, and race, under similar environmental conditions.
Anemia can be acute or chronic.
Anemia occurs when there is a decrease in the number of leukocyte precursors in the bone marrow.
A type of anemia that is usually associated with traumatic conditions such as an accident or severe injury and an anemia that may occur during or after surgery.
Chronic Blood Loss Anemia
Acute Blood Loss Anemia
Aplastic Anemia
Iron deficiency Anemoa
A type of anemia that is frequently associated with disorders of the gastrointestinal (GI) tract, although chronic blood loss may be related to heavy menstruation in women or urinary tract abnormalities.
Chronic Blood Loss Anemia
Acute Blood Loss Anemia
Aplastic Anemia
Iron deficiency Anemoa
A full manifestation of iron deficiency anemia will exhibit ___________________ red cell pattern.
hypochromic and microcytic
Hyperchromic and microcytic
Hyperchromic and macrocytic
hypochromic and normocytic
A type of autoimmune hemolytic anemia that is due to immunoglobulin G (IgG) coating of erythrocytes with or without complement fixation.
Warm Autoimmune Hemolytic Anemia
Cold Autoimmune Hemolytic Anemia
Isoimmune Hemolytic Anemia
Drug Induced Hemolytic Anemia
Which granulocyte maturation stage does secondary granules occurs?
Myeloblast
Myelocyte
Promyelocyte
Metamyelocyte
The nucleus of this cell is eccentric and exhibits cartwheel like pattern and has well-defined hof/perinuclear halo in the cytoplasm
Plasmablast
Plasma cell
Monocyte
Small Lymphocyte
It is a plasma cell with red to pink cytoplasm that is found in multiple myeloma.
Tart Cell
LE cell
Flame cell
Hairy Cell
This lipid storage disease is mainly due to deficiency in Glucocerebrosidase or Beta-glucosidase.
Gaucher's Disease
Niemann-pick Disease
Tay-Sachs
Sandhoff
It formed from degenerated /disintegrated nucleus of a ruptured white blood cell usually found in Chronic Lymphocytic
Leukemia (CLL).
Tart Cell
LE cell
Flame cell
Basket cell
