Pathophysiology Module 5 Mcqs 2022-23

Pathophysiology Module 5 Mcqs 2022-23

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1. What changes occur in peripheral blood at chronic lymphoblastic leukemia?

 
 
 
 

2. The components of anticoagulation system are:

 
 
 
 

3. Lack of vitamin K leads to:

 
 
 
 

4. Chronic leukemias are characterized by :

 
 
 
 

5. Extrinsic pathway of clotting factors is measured by?

 
 
 
 

6. The count of platelets lead to hemorrhagic syndrome:

 
 
 
 

7. Idiopathic thrombocytopenic purpura is example of a :

 
 
 
 

8. Life span of transfused RBC?

 
 
 
 

9. Iron deficiency anemia is seen with all of the following, except:

 
 
 
 

10. Which cells present in peripheral blood at chronic myeloid leukemia?

 
 
 
 

11. Components of anticoagulant system are:

 
 
 
 

12. Factors which induce platelet aggregation?

 
 
 
 

13. Thrombogenesis is promoted by all factors, except:

 
 
 

14. Chronic myeloid leukemia is associated with:

 
 
 
 

15. Hemosthasiopathias – are the disturbances of :

 
 
 
 

16. What kind of changes occurs in peripheral blood during acute myeloblastic leukemia?

 
 
 
 

17. Eosinophilia is:

 
 
 
 

18. Signs of a regenerative shift to the left are all listed, except:

 
 
 
 

19. The coagulation disorder with disturbance of the 2nd stage of blood coagulation is:

 
 
 
 

20. Microcytic hypochromic anemia is seen in:

 
 
 
 

21. Coagulation disorders are:

 
 
 
 

22. Nuclear shift shows :

 
 
 
 

23. Hiatus leukemicus is the absence of:

 
 
 
 

24. Following are seen in polycythemia vera, except:

 
 
 
 

25. Leukopenia may be a result of :

 
 
 
 

26. What concerns to hemorrhagic hemostasiopathias

 
 
 
 

27. Hematocrit during simple normovolemia is:

 
 
 

28. Typical signs of neutrophilic leukocytosis are:

 
 
 
 

29. Earliest feature of correction of iron deficiency anemia is:

 
 
 
 

30. Hodgkin,s lymphoma is caused by:

 
 
 
 

31. Which factor can initiate blood coagulation?

 
 
 
 

32. The major constituent of red thrombus is:

 
 
 
 

33. Hematocrit during oligocythemic normovolemia is:

 
 
 

34. What platelet factor takes part in the prothrombinase synthesis?

 
 
 
 

35. In aleukemic type of leukemias :

 
 
 
 

36. Dehydration leads to:

 
 
 

37. Increased count of eosinophils and basophils can be observed at:

 
 
 
 

38. What is the cause of hemorrhagic syndrome during leukemia?

 
 
 
 

39. One of the developmental stages of neutrophylic leukocyte is :

 
 
 
 

40. All are seen in thalassemia major, except:

 
 
 
 

41. Reticulocytes are stained with:

 
 
 
 

42. The causes of hemorrhagic angiopathias – are:

 
 
 
 

43. Antiaggregant for thrombocytes is:

 
 
 
 

44. The endothelial cells of intact vessels prevent blood coagulation by secretion of:

 
 
 
 

45. The main sign of trombophilic hemostasiopathias is:

 
 
 
 

46. Index of the nuclear shift is relation:

 
 
 
 

47. The main sign of hemorragic hemostasiopathia is:

 
 
 

48. Glucose-6-phosphate dehydrogenase helps in maintaining the integrity of RBC by:

 
 
 
 

49. Von Willebrand disease is:

 
 
 
 

50. Reticulocytosis is not seen in:

 
 
 
 

51. Fibrinolytics – are:

 
 
 
 

52. What kind of cells in the peripheral blood indicates acute myeloid leukemia?

 
 
 
 

53. Fibrin-split products stimulate:

 
 
 
 

54. Lack of calcium leads to:

 
 
 
 

55. What disease is accompanied with eosinophilia?

 
 
 
 

56. Inhibition of erythropoesis leads to:

 
 
 

57. The physiologic leukocytosis occurs in :

 
 
 
 

58. Physiologic leukocytosis occurs:

 
 
 

59. Signs of degenerative shift to the left are all listed, except:

 
 
 
 

60. Henoch-Schonlein purpura is :

 
 
 
 

61. The factor which converts the prothrombin to thrombin :

 
 
 
 

62. Compensatory mechanism of 2 stage of acute post-hemorrhagic anemia is:

 
 
 
 

63. Compensatory mechanisms of 1 stage of acute post-hemorrhagic anemia include all listed, except:

 
 
 
 

64. Chronic lymphoid leukemia is characterized by:

 
 
 
 

65. The main signs of chronic leukemias in hemogram are :

 
 
 
 

66. Acute leukemia is characterized by:

 
 
 
 

67. The major constituent of white thrombus is:

 
 
 
 

68. All of the following are true regarding hemolytic anemia, except:

 
 
 
 

69. Extrinsic coagulation pathway of hemostasis includes activation of:

 
 
 
 

70. The cause of the coagulation disorder with disturbance of the 3ed stage of blood coagulation are:

 
 
 
 

71. The anticoagulative effect of plasmin is realized through:

 
 
 
 

72. The coagulation disorders are:

 
 
 
 

73. What kind of changes occurs in peripheral blood during chronic myeloid leukemia?

 
 
 
 

74. One of the developmental stages of lymphocyte is:

 
 
 
 

75. Leukemoid reaction is characterized by:

 
 
 
 

76. Which causes can lead to the death during leukemia?

 
 
 
 

77. Normal value of color index is:

 
 
 
 

78. Substances can split the fibrin molecule?

 
 
 
 

79. Deficiency of what factor leads to hemophilia A?

 
 
 
 

80. Lack of plasmin leads to disorder of:

 
 
 
 

81. Acute myelogenous leukemia is characterized bу:

 
 
 
 

82. Inducers of platelets aggregation are:

 
 
 
 

83. Increased osmotic fragility is characteristic of:

 
 
 
 

84. Hematocrit during polycythemic normovolemia is:

 
 
 

85. Deficiency of prothrombin leads to disorder of:

 
 
 
 

86. All cause reticulocytosis, except:

 
 
 
 

87. Chronic hypoxia leads to:

 
 
 

88. Substances can split the fibrin molecule?

 
 
 
 

89. The causes of thrombocytopenia are:

 
 
 
 

90. Trombohemorrhagic hemostasiopathias is a kind of pathology with:

 
 
 
 

91. The synthesis of thrombin is blocked by

 
 
 
 

92. Deficiency of what factor leads to hemophilia B?

 
 
 
 

93. What changes occur in peripheral blood at acute lymphoblastic leukemia?

 
 
 
 

94. Hemophilia is a:

 
 
 
 

95. Type of leukocytes increase in allergic reactions more often :

 
 
 
 

96. Administration of cytostatics leads to:

 
 
 
 

97. Percentage of blasts in acute myeloid leukemia:

 
 
 

98. The sign of agranulocytosis is:

 
 
 
 

99. Morphologically recognized granulocytic cell is:

 
 
 
 

100. Factors which induce platelet aggregation

 
 
 
 

101. Deficiency of fibrinogen leads to disorder of :

 
 
 
 

102. What diseases are often accompanied with monocytosis?

 
 
 
 

103. The platelet-vascular hemostasis is necessary for:

 
 
 
 

104. Acute leukemia differs from chronic one by:

 
 
 
 

105. Disturbances of blood coagulation lead to:

 
 
 
 

106. Acute purulent inflammatory processes lead to :

 
 
 
 

107. Endoerythrocytic hemolytic anemias are:

 
 
 
 

108. The nuclear shift to the left (regenerative) is:

 
 
 
 

109. We should differentiate leukemoid reaction of neutrophil type with:

 
 
 
 

110. Compensatory mechanism of 3 stage of acute post-hemorrhagic anemia is

 
 
 
 
 

111. The functions of platelets in hemostasis are:

 
 
 
 

112. What is leukemia?

 
 
 
 

113. Mechanisms of leukopenia are :

 
 
 
 

114. GLUT present on surface of RBC?

 
 
 
 

115. DIC may be caused by:

 
 
 
 

116. Leukopenia may be a result of :

 
 
 
 

117. The function of the neutrophils is:

 
 
 
 

118. Chronic myeloid leukemia is characterized by:

 
 
 
 

119. What are the main changes in the hemogram during acute leukemia?

 
 
 
 

120. Procoagulant activity of the endothelium is caused by the production of:

 
 
 
 

121. Platelet precursor is:

 
 
 
 

122. Vitamin B12 deficiency results in:

 
 
 
 

123. RBC contains?

 
 
 
 

124. The nuclear shift to the right is the increase of the:

 
 
 
 

125. What leukocytes present in the peripheral blood of healthy people?

 
 
 
 

126. Leucopenia is not seen in:

 
 
 

127. Thrombogenic property of the endothelium is caused by production of:

 
 
 
 

128. What disease can lead to eosinophilia?

 
 
 
 

129. The types of nuclear shift to the right are:

 
 
 
 

130. Anticoagulant system is aimed at:

 
 
 
 

131. activation of blood coagulation

 
 
 
 

132. What type of leukocytes increases in viral infection?

 
 
 
 

133. Granulocytes are formed in

 
 
 
 

134. The cause of the coagulation disorders with disturbance of the first phase of blood coagulation is the deficiency of:

 
 
 
 


 

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