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[Mock Boards] HEMA exam with correct answers 2024 GRADED A+

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1. Which of the following is the anticoagulant of choice for most coagulation studies A. Sodiumoxalate B. Heparin C. SodiumCitrate D. EDTA E. Noneofthechoices correct answers C. SodiumCitrate 2. What would be the most likely designation by the WHO for the FAB AML M3 by the French-American-British classification? A. AMLwitht(15;17) B. AMLwitht(8;21) C. AMLwithmixedlineage D. AMLwithinv(16) E. noneofthesechoices correct answers A. AMLwitht(15;17) Which of the following findings would be most typical of severe septicemia? A. Toxicgranulation B. Hypersegmentation C. Auerrods D. Alder-Reillyanomaly E. noneofthesechoices correct answers A. Toxicgranulation The absence of the Philadelphia chromosome in granulocytic leukemia suggests: A. GoodPrognosis B. Rapidprogressionofthedisease C. Excellentresponsetotherapy D. Apolyclonalorigintothedisease E. Conversionfromanothermyeloproliferativedisorder correct answers B. Rapidprogressionofthedisease Approximately ____ of the total number of platelets circulate in the systemic circulation? A. One-fourth B. One-half C. One-third D. Two-third E. noneofthesechoices correct answers D. Two-third Which results are associated with hemophilia A? A. ProlongedAPTT,normalPT B. ProlongedAPTTandPT

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[Mock Boards] HEMA
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[Mock Boards] HEMA

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[Mock Boards] HEMA

1. Which of the following is the anticoagulant of choice for most coagulation
studies
A. Sodiumoxalate
B. Heparin
C. SodiumCitrate
D. EDTA
E. Noneofthechoices correct answers C. SodiumCitrate

2.What would be the most likely designation by the WHO for the FAB
AML M3 by the French-American-British classification?
A. AMLwitht(15;17)
B. AMLwitht(8;21)
C. AMLwithmixedlineage
D. AMLwithinv(16)
E. noneofthesechoices correct answers A. AMLwitht(15;17)

Which of the following findings would be most typical of severe
septicemia?
A. Toxicgranulation
B. Hypersegmentation
C. Auerrods
D. Alder-Reillyanomaly
E. noneofthesechoices correct answers A. Toxicgranulation

The absence of the Philadelphia chromosome in granulocytic leukemia
suggests:
F. GoodPrognosis
G. Rapidprogressionofthedisease
H. Excellentresponsetotherapy
I. Apolyclonalorigintothedisease
J.Conversionfromanothermyeloproliferativedisorder correct
answers B. Rapidprogressionofthedisease

Approximately of the total number of platelets circulate in
the systemic circulation?
K. One-fourth
L. One-half
M. One-third
N. Two-third
O. noneofthesechoices correct answers D. Two-third

Which results are associated with hemophilia A?
P. ProlongedAPTT,normalPT
Q. ProlongedAPTTandPT

,C. ProlongedPT,normalAPTT
D. NormalPTandAPTT
E. noneofthesechoices correct answers A. ProlongedAPTT,normalPT

Primary granules in the neutrophil appear at which stage:
A. Myeloblast
B. Myelocyte
C. Metamyelocyte
D. Promyelocyte
E. noneofthesechoices correct answers D. Promyelocyte

Platelet function is impaired after ingesting aspirin because:
F.Aspirinblockscertainglycoproteinreceptorsonthesurfaceofthe
platelet B.
Aspirininterfereswithliversynthesisofanumberofcoagulationfactor
s
C. Aspirinaltersthestructureoftheglycocalyx
D. Aspirin decreases thromboxaneA2 formationby inhibiting
cyclooxygenase correct answers D. Aspirin decreases thromboxaneA2
formationby inhibiting cyclooxygenase

Which of the following is most closely associated with acute promyelocytic
leukemia?
G. Ringedsideroblasts
H. Micromegakaryocytes
I. DisseminatedIntravascularCoagulation
J. Philadelphiachromosome
K. noneofthesechoices correct answers C.
DisseminatedIntravascularCoagulation

The test reagent in APTT contains which of the following substance(s)?
1. Citrated plasma, 2. Calcium ions, 3. Tissue thromboplastin, 4.
Phospholipids
L. 1,2,and3
M.2and4
N. 1and3
O. Only4 correct answers B. 2and4

Which of the following abnormalities is consistent with the
presence of lupus anticoagulant?

P. ShortenedAPTT/bleedingcomplications
Q. ProlongedAPTT/thrombosis
R. ProlongedAPTT/thrombocytosis
S. Thrombocytosis/thrombosis
T. noneofthesechoices correct answers B.
ProlongedAPTT/thrombosis

Platelet aggregation studies revealed normal aggregation curves with
collagen, epinephrine, and ADP, but an abnormal aggregation curve with
ristocetin. Based on these findings, what is the differential diagnosis?
U. VonWillebranddiseaseandBernard-Souliersyndrome
V. Glanzmann'sthrombastheniaandvonWillebranddisease

, C. StoragepooldiseaseandGlanzmann'sthrombasthenia
D. Bernard-Souliersyndromeandstoragepooldisease
E. noneofthesechoices correct answers A.
VonWillebranddiseaseandBernard- Souliersyndrome

The Philadelphia chromosome is formed by a translocation between
the:

A. longarmofchromosome21andlongarmofchromosome9
B. longarmofchromosome21andshortarmofchromosome6
C. longarmofchromosome22andlongarmofchromosome9
D. longarmofchromosome22andshortarmofchromosome6
E.noneofthesechoices correct answers C.
longarmofchromosome22andlongarmofchromos
ome9

Platelet adhesion is abnormal in Bernard-
Soulier disease because:

F. Aplasmafactorneededforplateletadhesionisab
sent
G. Antibodiestophospholipidarepresent
H. GlycoproteinIboftheplateletmembraneisdefec
tive
I. Abnormalproteinsintheplasmacoattheplatelet
membrane
J.noneofthesechoices correct answers
C.
GlycoproteinIboftheplateletmembraneisdef
ective

Morphologic variants of plasma cells do
not include:

K. Flamecells
L. Grapecells
M. Morulacells
N. Gauchercells
O. noneofthesechoices correct answers D.
Gauchercells

Which ratio of anticoagulant to blood is
correct for coagulation studies

P. 1:4
Q. 1:9
R. 1:5
S. 1:10
T. noneofthesechoices correct answers B.
1:9

In differentiating the maturation stages of the megakaryocytic cells,
emphasis should be placed on the .

U. Cytoplasmicappearance
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