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Pathology MCQ
PHASE 1
1.Which of the following appear in the red cells
of Ivemark syndrome/asplenic individuals?
a. Macroovalocytosis
b. Basophilic stippling
c. Howell-Jolly bodies
d. Target cells
2. The life span of platelets in circulation is
about?
a. 1 to 3 days
b.3 to 5 days
c. 5 to 7 days
d. 7 to 10 days
3. A 13 yr old child suffered from dysentery one
week ago, currently complaining of hematuria
and raised serum creatinine. PBS examination
is expected to show:
a. Target cell
b. Spherocyte
c. Schistocyte
d. Bite cell
4. HbC is best illustrated
as?
a. Α2ß2
3Glu→Lys
b. Α2ß2
4Glu→Lys
c. Α2ß2
5Glu→Lys
d. Α2ß2
6Glu→Lys
5. The 4T ‘s scoring system for pre-test
probability of HIT includes all except:
a. Thrombocytopenia
b. Timing of platelet count fall
c. Thrombosis
d. Treatment dose
6.In comparison to myeloma,which is more
frequent in plasma cell leukemia:
a. Osteolytic lesion
b. Bone pain
c. Renal failure
d. All of the above
7. Leukaemia with t(15;17)(q22;q12) usually has
the immunophenotype:
a. CD13,CD33,CD15,CD117
b. CD13,CD33,CD117,HLADR
c. CD13,CD33,CD117,cMPO
d. CD13,CD33,CD15,cMPO
8. Match the following with respect to iron deficiency
anaemia:
a. Red cell zinc
protoporphyrin (ZPP)
b. Serum transferrin
receptor
c. Transferrin saturation
d. Hepcidin
1. Increases
2. Decreases
3. Increases
4. Decreases
9. Which of the following is safe in therapeutic
doses in patients with G6PD deficiency:
a. Primaquine
b. Acetaminophen
c. Sulfamethoxazole
d. Dapsone
10. The affinity of haemoglobin for Oxygen is
decreased by all except:
a. Fever
b. Alkalosis
c. Binding of CO2
d. Binding of 2,3-DPG
11. An Increased percentage of HbA2 is
expected in :
a. αthal trait
b. ßthal trait
c. δßthal trait
d. All of the above
12. A 15 yr old child presents with fever and generalised
petechiae, lab investigation reveal:
• Hb 6gm% MCV = 105fl MCH = 30pg
• WBC = 1.2 X 109 /L PC = 10 X 109 /L
• LYMP%- 73%, GRAN%-25%,MID%-2%
• BM: Hypo cellular. What is the most likely diagnosis?
a. Severe aplastic anemia
b. Very severe aplastic anemia
c. Nonsevere aplastic anemia
d. Hypoplastic MDS
13. All are direct thrombin inhibitors except:
a. Fondaparinux sodium
b. Bivalirudin
c. Argatroban
d. Lepirudin
14. For the given coagulation work up results which is the
most probable diagnosis:
• BT- 5 min
• PT- 11 sec ( 10 sec)
• APTT- 50sec (32 sec)
• Mixing study with factor IX deficient plasma: APTT – 40
sec
a. Hemophilia A
b. Hemophilia B
c. Hemophilia C
d. Factor VIII inhibitor positive
15. Regarding febrile nonhemolytic transfusion
reaction false is:
a.More common in multiply transfused patients
b.HLA antibodies are most common
c. Leucodepletion of blood products is not
helpful
d.Due to transfusion of cytokines
16. Which is not a GpIIb/IIIa inhibitor:
a. Abciximab
b. Eptifibatide
c. Tirofiban
d. Argatroban
17.Haemolytic disease of new
born(erythroblastosis fetalis ) is an example
of:
a. Type I hypersenstivity
b. Type II hypersenstivity
c. Type III hypersenstivity
d. Type IV hypersenstivity
18. Pre-transfusion cross-match is not required
for:
a. Cryoprecipitate
b. pRBC
c. FFP
d. Granulocyte tranfusion
19. Neutrophilia is seen in all except:
a.Leucocyte adhesion defect
b.Steroid administration
c. Lithium therapy
d.Kostmann syndrome
20. Infectious complications of blood transfusion
may result from all except:
a. HTLV I
b. HTLV II
c. West Nile virus
d. None of the above
21. Good prognosis ALL:
a. t(4;11)
b. t(9;22)
c. t(12;21)
d. t(1;19)
22. For diagnosis of Smoldering Myeloma, false
is:
a. BM plasma cells ≤ 10%
b. Absence of anemia
c. Serum monoclonal protein ≥ 3g/dl
d. None of the above
23. IPSS for MDS includes all except:
a.Marrow blast %
b.Karyotype
c. Cytopenias
d.Age
24. Hairy cell leukaemia , immunophenotype:
a. Bright CD20,CD10,CD25,CD103
b. Dim CD20,CD10,CD25,CD103
c. Bright CD20,CD11c,CD25,CD103
d. Dim CD20,CD11c,CD25,CD103
25. WHO definition of anaemia in pregnancy
requires Hb below:
a. 10g%
b. 11g%
c. 12g%
d. 13g%
26. Albino child with repeated
infection
most probable diagnosis:
a. Grescilli syndrome
b. Chediac Higashi syndrome
c. Dohle bodies
d. Toxic granules
27.
Comment on
PBS:
28.
Identify the cell
with arrow head:
a.Gaucher cell
b.Mott cell
c.Histoplasma
inclusion
d.Fungal bodies
29.
Identify the
abnormality in
the Karyotype
30.Identify the cytogenetic finding shown in
the FISH metaphase spread.

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Path_MCQ.ppt

  • 2. 1.Which of the following appear in the red cells of Ivemark syndrome/asplenic individuals? a. Macroovalocytosis b. Basophilic stippling c. Howell-Jolly bodies d. Target cells
  • 3. 2. The life span of platelets in circulation is about? a. 1 to 3 days b.3 to 5 days c. 5 to 7 days d. 7 to 10 days
  • 4. 3. A 13 yr old child suffered from dysentery one week ago, currently complaining of hematuria and raised serum creatinine. PBS examination is expected to show: a. Target cell b. Spherocyte c. Schistocyte d. Bite cell
  • 5. 4. HbC is best illustrated as? a. Α2ß2 3Glu→Lys b. Α2ß2 4Glu→Lys c. Α2ß2 5Glu→Lys d. Α2ß2 6Glu→Lys
  • 6. 5. The 4T ‘s scoring system for pre-test probability of HIT includes all except: a. Thrombocytopenia b. Timing of platelet count fall c. Thrombosis d. Treatment dose
  • 7. 6.In comparison to myeloma,which is more frequent in plasma cell leukemia: a. Osteolytic lesion b. Bone pain c. Renal failure d. All of the above
  • 8. 7. Leukaemia with t(15;17)(q22;q12) usually has the immunophenotype: a. CD13,CD33,CD15,CD117 b. CD13,CD33,CD117,HLADR c. CD13,CD33,CD117,cMPO d. CD13,CD33,CD15,cMPO
  • 9. 8. Match the following with respect to iron deficiency anaemia: a. Red cell zinc protoporphyrin (ZPP) b. Serum transferrin receptor c. Transferrin saturation d. Hepcidin 1. Increases 2. Decreases 3. Increases 4. Decreases
  • 10. 9. Which of the following is safe in therapeutic doses in patients with G6PD deficiency: a. Primaquine b. Acetaminophen c. Sulfamethoxazole d. Dapsone
  • 11. 10. The affinity of haemoglobin for Oxygen is decreased by all except: a. Fever b. Alkalosis c. Binding of CO2 d. Binding of 2,3-DPG
  • 12. 11. An Increased percentage of HbA2 is expected in : a. αthal trait b. ßthal trait c. δßthal trait d. All of the above
  • 13. 12. A 15 yr old child presents with fever and generalised petechiae, lab investigation reveal: • Hb 6gm% MCV = 105fl MCH = 30pg • WBC = 1.2 X 109 /L PC = 10 X 109 /L • LYMP%- 73%, GRAN%-25%,MID%-2% • BM: Hypo cellular. What is the most likely diagnosis? a. Severe aplastic anemia b. Very severe aplastic anemia c. Nonsevere aplastic anemia d. Hypoplastic MDS
  • 14. 13. All are direct thrombin inhibitors except: a. Fondaparinux sodium b. Bivalirudin c. Argatroban d. Lepirudin
  • 15. 14. For the given coagulation work up results which is the most probable diagnosis: • BT- 5 min • PT- 11 sec ( 10 sec) • APTT- 50sec (32 sec) • Mixing study with factor IX deficient plasma: APTT – 40 sec a. Hemophilia A b. Hemophilia B c. Hemophilia C d. Factor VIII inhibitor positive
  • 16. 15. Regarding febrile nonhemolytic transfusion reaction false is: a.More common in multiply transfused patients b.HLA antibodies are most common c. Leucodepletion of blood products is not helpful d.Due to transfusion of cytokines
  • 17. 16. Which is not a GpIIb/IIIa inhibitor: a. Abciximab b. Eptifibatide c. Tirofiban d. Argatroban
  • 18. 17.Haemolytic disease of new born(erythroblastosis fetalis ) is an example of: a. Type I hypersenstivity b. Type II hypersenstivity c. Type III hypersenstivity d. Type IV hypersenstivity
  • 19. 18. Pre-transfusion cross-match is not required for: a. Cryoprecipitate b. pRBC c. FFP d. Granulocyte tranfusion
  • 20. 19. Neutrophilia is seen in all except: a.Leucocyte adhesion defect b.Steroid administration c. Lithium therapy d.Kostmann syndrome
  • 21. 20. Infectious complications of blood transfusion may result from all except: a. HTLV I b. HTLV II c. West Nile virus d. None of the above
  • 22. 21. Good prognosis ALL: a. t(4;11) b. t(9;22) c. t(12;21) d. t(1;19)
  • 23. 22. For diagnosis of Smoldering Myeloma, false is: a. BM plasma cells ≤ 10% b. Absence of anemia c. Serum monoclonal protein ≥ 3g/dl d. None of the above
  • 24. 23. IPSS for MDS includes all except: a.Marrow blast % b.Karyotype c. Cytopenias d.Age
  • 25. 24. Hairy cell leukaemia , immunophenotype: a. Bright CD20,CD10,CD25,CD103 b. Dim CD20,CD10,CD25,CD103 c. Bright CD20,CD11c,CD25,CD103 d. Dim CD20,CD11c,CD25,CD103
  • 26. 25. WHO definition of anaemia in pregnancy requires Hb below: a. 10g% b. 11g% c. 12g% d. 13g%
  • 27. 26. Albino child with repeated infection most probable diagnosis: a. Grescilli syndrome b. Chediac Higashi syndrome c. Dohle bodies d. Toxic granules
  • 29. 28. Identify the cell with arrow head: a.Gaucher cell b.Mott cell c.Histoplasma inclusion d.Fungal bodies
  • 31. 30.Identify the cytogenetic finding shown in the FISH metaphase spread.