1.

Chronic liver disease, massive bleeding, surgery

2. Purpura, dorsum of hands and forearns, old people

3. Prol bleeding, tooth extraction, essential for normal blood coag

(Mga ions and vitamins an choices)

4. Bleeding patients, scurvy

5. 8:00

6. Bleeding, umbilical stump, newborn, mother w/ vit K deficiency

A. Hemolytic disease of newborn
B. Hemorrhagic disease of newborn
C.
D.

7. Factors, requires vit K

8. Bleeding, prol biliary obstruction

9. Not involved in blood coag

A. Platelet
B. Prothrombin
C. Erythropoietin
D. Fibrinogen

10. Petechiae, purpura on the arms and legs, spontaneous bleeding, platelet count is
low

11. Most common cause, acquired qualitative platelet disorder

A. Drugs
B.
C.
D.

12. Can inh platelet function

A. Penicillin
B. Uremia
C. Myeloproliferative disorder

13. Bleeding time

14. Blood, stored in ref for 1 week, results in

A. Inc platelet
B. Dec platelet
C. No change

15. Not performed by platelets

A. Clot retraction
B. Conversion of fibrinogen to fibrin
C. Hemostatic plug

16. Thrombotic eps, digestion of fibrin effected by

17. Fibrin clot hydrolyzed, what substance is produced

18. Coag factors synthesized in what organ

A. Spleen
B. Liver
C. Bone marrow

19. Contraction or retraction of formed clot

20. Test, extrinsic pathway mechanism

21. Activates fibrinogen

22. Converts fibrinogen to fibrin

23. Complete action of plasma coagulation factors, test

A.
B. Thrombin time
C. Bleeding time
D. Coag time

24. Factor deficiency, prol PT and PTT

A.
B. F 5
C. F 5 and 10
D. F 7,9,11

25. Pathway, conversion of f 10 to 10a

A. Extrinsic
B. Intrinsic

26. Bleeding, DIC

A. Thrombocytopenia w/ fibrinogenopenia
B. Deficiency of vit K rel factors
C. Normal platelet count
D. Deficiency of plasmin

27. Abn coag time

28. Platelets are produced in the

29. Chem released, platelet aggregation

A. Thromboxane
B. Thrombin
C. Thromboplastin
D.
30. Thrombocytopenia, except
A. Hyposplenism
B. Aplastic anemia
C. Acute leukemia
D. Long term anti coag

31. Prol ingestion of salicylates, effect on platelets

32. Phospholipid on surface of platelet

A.
B.
C. Factor 3
D.

33. Substance not found in blood under ordinary conditions

A. Plasmin
B. Thrombin
C. FDP
D. Nota

34. Tested by clot retraction time

35. Actual digestion of fibrin effected by

36. Fibrin clot hydrolyzed, what substance is prod

37. Formation of hemostatic plug accom plug

A. Prod
B. Function
C. Dilution
D. Destruction
38. Acute DIC
39. Bone marrow infiltration
40. HIV
41. Malaria, splenomegaly
42. ITP
43. Leukemic infil of BM
44. Megaloblastic anemia
45. Prosthetic heart valves
46. Abruptio placenta
47. Salicylates

48. Hemorrhagic syndrome, uncontrolled pro coag, fibrin depo in microvasculature

49. Specific cell, platelet is derived from
50. In vivo aggregation of platelets via fibrin

1. Cellularity 20%
A. Normocellular marrow
B. Hypocellular marrow
C. Hypercellular marrow
D.

2. Cytoplasmic abn, except

A. May hegglin
B. Dohle bodies
C. Pelger huet
D.

3. Movement of leukocyte impaired

A. Lazy leukocyte
B. Job's syndrome
C.
D.

4. Dist factor bet CML and leukomoid

A. Tear drop
B. No of WBC

5. Inh form of leukocyte disorder except

A. Alder reilly
B. Pelger huet
C. Dohle
D. Chediak higashi

6. Erythrocytosis, thrombocytosis, erythropoietin dec, plasma vol high, something normal

A. Dehydration
B. Renal disease
C. Jak2 mutation
D. Paraneoplastic

7. Physiologic neutrophilia except

A. Pregnancy
B. Typhoid fever
C. Vomitting
D. Stress

8. Dry tap BM
A. Idiopathic
B.

9. Chronic myeloprolif disorders except

A. Idiopathic
B. Essential thrombocytopenia
C. CML
D. Polycythemia vera

10. Dohle bodies

11. Tear drop RBC

12. Large cytoplasmic granules

13. Philadelphia chromosome

14. Normal myeloid erythroid ratio

15. LAP, chronic myelogenous leukemia, w/o infection

16. Neutrophilia pronounced

17. Auer rods

18. Eosinophil attraction to parasites

A. T cell
B. B cell
C. Antibody

19. Cine qua non CML

20. Erythropoietin level, polycythemia vera

21. What are the PMNs

22. Normal newboorn, WBC differential

23. Physio var, affect leukocyte conc, except

A. Race
B. Time of day
C. Pregnancy
D. Height and weight

24. Marginating neutrophils, to roam freely, no. of circulating neutrophils

A. Double
C. Triple
D. Quadruple
E. No change

25. Not a cause of eosinophilia

A. Eczema
B. Steroid
C. Hodgkins
D. Hookworm

26. Acute bacterial infections, blood finding

27. Abn function, leukocytes

A. DM
B. Steroid
C. Folic acid deficiency
D.

28. Auer bodies

29. Blood cell, macrophage, from
A. Monocytes

30. CML
A. Leukocytosis
B. Inc LAP
D. Dec ME ratio

31. Cytoplasmic inclusion bodies, PMN, severe infections

32. Differentiation of granulocytes into 3 specific types, stage of maturation

33. Chronic granulomatous inflammation

A. Neutrophilia
B. Eosinophilia
C. Monocytosis
D.

34. Early stage, granulocyte, cytoplasmic granules are seen 1st

35. Enlarged, hypersegmentef neutrophils

36. Hyposegmented neutrophuls

37. Hypersplenism

38. Hypersensitivity type 1

39. Hypersplenism and BM

40. Aleukemic leukemia, BM

41. Leukocye not normally seen in peripheral blood

A.
B. Juvenile
C. Band

42. LAP dec

43. Leukomoid rxn, char

A. Leukocytosis, inc something
B. Leukocytosis, dec LAP
C. Leukocytosis, many blasts
D. Agranulocytosis, auer rods

44. Myelofibrosis, BM disorder

45. Myeloproliferative disorder except

A. Pernicious anemia
B. Polycythemia vera
C. CML
D. Erythroid leukemia

46. Philadelphia chromosome

47. Tissue necrosis, leukocytic response

48. Absolute lymphocytosis

49. Releases histamine, what cell

50. Antibodies producing cell