Hematology

1. Which of the following is not true in thrombotic thrombocytopenic purpura?

2. Coagulation factor deficient in stored blood is:

3. Malignancy of which lineage is associated with autoimmune haemolytic anemia?

4. Punctate basophilia is seen in all except:

5. Which isolated coagulation factor deficiency causes thrombosis?

6. Commonest pathogen involved in sickle cell anemia-induced osteomyelitis is:

7. G6PD may reflect a ‘false normal’ report in:

8. The presence of anemia, jaundice and splenomegaly with increased mean corpuscular haemoglobin concentration (MCHC) is seen in:

9. Red cell osmotic fragility is increased in:

10. Agranulocytosis may be seen in treatment with:

11. Acanthosis nigricans may be associated with all except:

12. Hand-Schwier-Christian disease does not have:

13. Sickle cell anaemia is not complicated by:

14. Which of the following is not seen in sickle cell anaemia?

15. Coombs positive haemolytic anaemia is a feature of:

16. Patients on aspirin will have:

17. Eosinophilia is a feature of:

18. All of the following produce microcytic anaemia except:

19. Splenectomy is contraindicated in:

20. Which of the following is not a myelodysplastic syndrome (MDS)?

21. Which of the following is not seen in hemolytic-uraemic syndrome?

22. The half-life of a platelet is:

23. Which test detects haemolytic anemia?

24. Platelet transfusion is not indicated in:

25. Sezary syndrome is:

26. Low-dose arsenic trioxide has recently been used in relapsed patients of:

27. Busulfan therapy may lead to all except:

28. All of the following are seen in intravascular haemolysis except:

29. Alopecia mucinosa may be seen in:

30. vW antigen level is increased in:

31. Iron transport protein is:

32. Total serum LDH is not raised in:

33. Palpable purpura is seen in:

34. Microcytic hypochromic anaemia is characteristic of:

35. Transient myeloproliferative disorder of the newborn is commonly seen in association with:

36. The most effective treatment of polycythaemia vera is:

37. Pelger-Huet anomaly is:

38. Immunoproliferative small intestinal disease (IPSID) is a variety of:

39. Which is not an example of microangiopathic haemolytic anemia?

40. Raised Fe and normal TIBC are found in:

41. Para-hemophilia is a deficiency of factor:

42. Leucocyte alkaline phosphatase (LAP) score is high in all except:

43. Leucocyte alkaline phosphatase (LAP) score is diminished in:

44. Pseudolymphoma may be produced by all except:

45. All of the following may cause pain abdomen in thalassaemia major except:

46. Increased serum iron and reduced iron-binding capacity are features of:

47. All are true regarding midline granuloma except:

48. Wiskott-Aldrich syndrome does not feature:

49. alpha-interferon is not beneficial in:

50. Schumm test is done to detect?