Hematology Home Hematology 0% 13 votes, 0 avg 40 Hematology Welcome to Hematology Quiz. There are 50 shot-stemmed, single-best type Hematology questions. We have a collection of over 100 questions. Contact us and get a free link in case you are interested. 1 / 50 1. Pseudolymphoma may be produced by all except: A. Cyclosporine B. Primidone C. Phenytoin D. Lithium 2 / 50 2. Hepatosplenomegaly with lymphadenopathy is found in all except: A. Lymphoma B. Chronic myeloid leukemia C. Disseminated tuberculosis D. Acute lymphatic leukemia 3 / 50 3. Which is not true in relation to multiple myeloma? A. Response to Melphalan B. Renal failure C. Hyperviscosity syndrome D. Moderate splenomegaly 4 / 50 4. Conditions resistant to malaria are all except: A. Thalassemia major B. Duffy -ve blood group C. Hb C disease D. Sickle cell disease 5 / 50 5. Low-dose arsenic trioxide has recently been used in relapsed patients of: A. Aplastic anemia B. Hairy cell leukemia C. Acute lymphoblastic leukemia D. Acute promyelocytic leukemia 6 / 50 6. Splenectomy is virtually curative in: A. G6PD deficiency B. Idiopathic thrombocytopenic purpura (ITP) C. Hereditary spherocytosis D. Thalassemia 7 / 50 7. Which of the following is contraindicated in polycythaemia vera? A. Low-dose aspirin B. Chlorambucil C. Hydroxyurea D. Interferon-a 8 / 50 8. Gum bleeding is characteristic of all except: A. Hemophilia B. Chronic phenytoin therapy C. Aplastic anaemia D. Scurvy 9 / 50 9. ‘Suggilations’ are haemorrhagic spots in the size of: A. 2-5 mm in diameter B. 1-2 mm in diameter C. > 20 mm in diameter D. > 10 mm in diameter 10 / 50 10. Features of sickle cell anaemia do not include: A. Leg ulcers B. Hypersplenism C. Priapism D. Nocturia 11 / 50 11. Giant lysosomal granules in granulocytes associated with albinism is known as: A. Schultz syndrome B. Niemann-Pick disease C. May-Hegglin anomaly D. Chediak-Higashi syndrome 12 / 50 12. The half-life of a platelet is: A. 10-12 days B. 1-2 days C. 3-4 days D. 5-6 days 13 / 50 13. Total serum LDH is not raised in: A. AMI B. Crush injury C. Hemolysis D. Stroke 14 / 50 14. All of the following may complicate bone marrow transplantation except: A. Leukoencephalopathy B. Emphysema C. Cataract formation D. Cardiomyopathy 15 / 50 15. In polycythaemia vera, which is not true? A. High ESR B. Increased LAP score C. High serum vitamin B12 level D. Low level of erythropoietin 16 / 50 16. Which of the following is associated with prolonged bleeding time? A. Antiphospholipid syndrome B. Hemophilia C. von Willebrand's disease D. Polycythaemia vera 17 / 50 17. Cooley’s anemia is: A. Megaloblastic anemia B. Thalassemia major C. Sickle cell anemia D. Aplastic anemia 18 / 50 18. Epitrochlear adenopathy may be produced by all except: A. Tularemia B. Leprosy C. Sarcoidosis D. Secondary syphilis 19 / 50 19. In chronic granulomatous disease, which is false? A. Diagnosed by amount of nitroblue tetrazolium reduction B. Difficulty in phagocytosis C. Prone to infection by staphylococci D. Neutrophil count is normal 20 / 50 20. Decreased iron and decreased iron-binding capacity are seen in: A. Menorrhagia B. Recurrent GI tract hemorrhage C. Intestinal resection D. Chronic infections 21 / 50 21. Coagulation factor deficient in stored blood is: A. IX B. II C. VII D. V 22 / 50 22. Macrocytic-hypochromic anemia is found in: A. Iron deficiency anemia B. Pernicious anemia C. Pregnancy D. Thalassemia 23 / 50 23. Which test detects haemolytic anemia? A. Benedict's test B. Coombs' test C. Schilling test D. Occult blood test in stool 24 / 50 24. Pancytopenia may develop from all except: A. Paroxysmal nocturnal hemoglobinuria (PNH) B. Acute myeloid leukemia (AML) C. Hemosiderosis D. Systemic lupus erythematosus 25 / 50 25. Which of the following may develop in sites other than bone marrow? A. Neutrophil B. Monocyte C. Lymphocyte D. Megakaryocyte 26 / 50 26. The commonest cause of jaundice in thalassaemia is: A. Viral hepatitis B B. Hemolysis C. Viral hepatitis C D. Iron deposition in liver 27 / 50 27. Acanthosis nigricans may be associated with all except: A. Ulcerative colitis B. Carcinoma of the stomach C. Stein-Leventhal syndrome D. Diabetes mellitus 28 / 50 28. Which of the following is not true in thrombasthenia? A. Normal platelet count B. Prolonged clotting time C. Prolonged bleeding time D. Platelet aggregation defect 29 / 50 29. Pelger-Huet anomaly is: A. Presence of Dohle bodies in neutrophils B. Faulty maturation of platelets C. Hereditary hyposegmentation of neutrophils D. Hereditary hypersegmentation of neutrophils 30 / 50 30. All of the following are true in paroxysmal nocturnal haemoglobinuria (PNH) except: A. Elevated red cell acetylcholinesterase B. Elevated LDH C. Positive acidified serum lysis (HAM) test D. Low leucocyte alkaline phosphatase 31 / 50 31. Busulfan therapy may lead to all except: A. Hyperpigmentation B. Optic neuritis C. Bone marrow suppression D. Pulmonary fibrosis 32 / 50 32. alpha-interferon is not beneficial in: A. Chronic granulomatous disease B. Chronic myeloid leukaemia C. Kaposi's sarcoma D. Hairy cell leukemia 33 / 50 33. Haemolytic anaemia is not produced by: A. Quinidine B. Penicillin C. Methyldopa D. Lithium 34 / 50 34. Leucoerythroblastic blood picture may be seen in all except: A. Myelophthisic anemia B. Sickle cell anemia C. Myelofibrosis D. Gaucher's disease 35 / 50 35. Serum alkaline phosphatase level in multiple myeloma is usually? A. High B. Low C. Fluctuates D. Normal 36 / 50 36. Which of the following factors is unstable in stored blood? A. V B. II C. VII D. X 37 / 50 37. Which of the following is not true in paroxysmal cold hemoglobinuria? A. Precipitated by exposure to cold B. Not a cold agglutinin disease C. Associated with mycoplasma infection D. IgG antibody-mediated 38 / 50 38. Microcytic hypochromic anaemia is characteristic of: A. Munchausen's syndrome B. Pseudohypoparathyroidism C. Persons who are true vegetarians D. Patterson-Kelly syndrome 39 / 50 39. Virchow’s node receives lymphatics from all except: A. Stomach B. Testes C. Prostate D. Breast (left) 40 / 50 40. Thymoma may be associated with all of the following except: A. Pure red cell aplasia B. Hypergammaglobulinaemia C. Cushing's syndrome D. Myasthenia gravis 41 / 50 41. Which of the following is not seen in hemolytic-uraemic syndrome? A. Thrombocytopenia B. Hypofibrinogenaemia C. Positive Coombs test D. High creatinine level 42 / 50 42. Hand-Schwier-Christian disease does not have: A. Hepatosplenomegaly B. Hypercholesterolemia C. Exophthalmos D. Diabetes mellitus 43 / 50 43. All the following drugs produce methemoglobinaemia except: A. Amyl nitrite B. Phenacetin C. Sodium nitroprusside D. Hydralazine 44 / 50 44. Migratory thrombophlebitis is commonly due to: A. Hepatocellular carcinoma B. Carcinoma of the pancreas C. Hypernephroma D. Bronchogenic carcinoma 45 / 50 45. Which of the following is not associated with a microangiopathic blood picture? A. Infectious mononucleosis (glandular fever) B. Thrombotic thrombocytopenic purpura C. Severe burns D. Meningococcal septicaemia 46 / 50 46. Commonest pathogen involved in sickle cell anemia-induced osteomyelitis is: A. Salmonella B. Nocardia C. Streptococcus D. Staphylococcus 47 / 50 47. Coombs positive haemolytic anaemia is a feature of: A. Polyarteritis nodosa (PAN) B. Hemolytic-uremic syndrome (HUS) C. Thrombotic thrombocytopenic purpura (TTP) D. Systemic lupus erythematosus (SLE) 48 / 50 48. The half-life of albumin is: A. 16-20 days B. 20-22 days C. 1-2 days D. 10-14 days 49 / 50 49. Which of the following is false in hereditary haemorrhagic telangiectasis? A. Telangiectasia in skin and mucous membrane B. May have hematemesis C. Telangiectasia does not blanch on pressure D. Positive familial pattern 50 / 50 50. Packed red cells are constructed by: A. Precipitation B. Centrifugation C. Filtration D. Sedimentation LinkedIn Facebook Twitter VKontakte Visit our FB page Restart Quiz Send Feedback Previous Post Pulmonology Next Post Neurology